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Sample records for aerosol direct effect

  1. 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.

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

    SciTech Connect

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

    2011-06-21

    The direct and semi-direct radiative effects of biomass burning aerosols from Southern African fires during July-October are investigated using 20 year runs of the Community Atmospheric Model (CAM) coupled to a slab ocean model. The aerosol optical depth is constrained using observations in clear skies from MODIS and for aerosol layers above clouds from CALIPSO. Over the ocean, where the absorbing biomass burning aerosol layers are primarily located above cloud, negative top of atmosphere (TOA) semi-direct radiative effects associated with increased low cloud cover dominate over a weaker positive all-sky direct radiative effect (DRE). In contrast, over the land where the aerosols are often below or within cloud layers, reductions in cloud liquid water path (LWP) lead to a positive semi-direct radiative effect that dominates over a near-zero DRE. Over the ocean, the cloud response can be understood as a response to increased lower tropospheric stability (LTS) which is caused both by aerosol absorptive warming in overlying layers and surface cooling in response to direct aerosol forcing. The ocean cloud changes are robust to changes in the cloud parameterization (removal of the hard-wired dependence of clouds on LTS), suggesting that they are physically realistic. Over land where cloud cover changes are minimal, decreased LWP is consistent with weaker convection driven by increased static stability. Over the entire region the overall TOA radiative effect from the biomass burning aerosols is almost zero due to opposing effects over the land and ocean. However, the surface forcing is strongly negative requiring a reduction in precipitation. This is primarily realized through reductions in convective precipitation on both the southern and northern flanks of the convective precipitation region spanning the equatorial rainforest and the ITCZ in the southern Sahel. The changes are consistent with the low-level aerosol forced cooling pattern. The results highlight the

  3. 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.

  4. 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

  5. Quantifying Aerosol Direct Effects from Broadband Irradiance and Spectral Aerosol Optical Depth Observations

    SciTech Connect

    Creekmore, Torreon N.; Joseph, Everette; Long, Charles N.; Li, Siwei

    2014-05-16

    We outline a methodology using broadband and spectral irradiances to quantify aerosol direct effects on the surface diffuse shortwave (SW) irradiance. Best Estimate Flux data span a 13 year timeframe at the Department of Energy Atmospheric Radiation Measurement Program’s Southern Great Plains (SGP) site. Screened clear-sky irradiances and aerosol optical depth (AOD), for solar zenith angles ≤ 65°, are used to estimate clear-sky diffuse irradiances. We validate against detected clear-sky observations from SGP’s Basic Radiation System (BRS). BRS diffuse irradiances were in accordance with estimates, producing a root-mean-square error and mean bias errors of 4.0 W/m2 and -1.4 W/m2, respectively. Absolute differences show 99% of estimates within ±10 W/m2 (10%) of the mean BRS observations. Clear-sky diffuse estimates are used to derive quantitative estimates of aerosol radiative effects, represented as the aerosol diffuse irradiance (ADI). ADI is the contribution of diffuse SW to global SW, attributable to scattering of atmospheric transmission by natural plus anthropogenic aerosols. Estimated slope for the ADI as a function of AOD indicates an increase of ~22 W/m2 in diffuse SW for every 0.1 increase in AOD. Such significant increases in the diffuse fraction could possibly increase photosynthesis. Annual mean ADI is 28.2 W/m2, and heavy aerosol loading at SGP provides up to a maximum increase of 120 W/m2 in diffuse SW over background conditions. With regard to seasonal variation, the mean diffuse forcings are 17.2, 33.3, 39.0, and 23.6 W/m2 for winter, spring, summer, and fall, respectively.

  6. Influence of Observed Diurnal Cycles of Aerosol Optical Depth on Aerosol Direct Radiative Effect

    NASA Technical Reports Server (NTRS)

    Arola, A.; Eck, T. F.; Huttunen, J.; Lehtinen, K. E. J.; Lindfors, A. V.; Myhre, G.; Smirinov, A.; Tripathi, S. N.; Yu, H.

    2013-01-01

    The diurnal variability of aerosol optical depth (AOD) can be significant, depending on location and dominant aerosol type. However, these diurnal cycles have rarely been taken into account in measurement-based estimates of aerosol direct radiative forcing (ADRF) or aerosol direct radiative effect (ADRE). The objective of our study was to estimate the influence of diurnal aerosol variability at the top of the atmosphere ADRE estimates. By including all the possible AERONET sites, we wanted to assess the influence on global ADRE estimates. While focusing also in more detail on some selected sites of strongest impact, our goal was to also see the possible impact regionally.We calculated ADRE with different assumptions about the daily AOD variability: taking the observed daily AOD cycle into account and assuming diurnally constant AOD. Moreover, we estimated the corresponding differences in ADREs, if the single AOD value for the daily mean was taken from the the Moderate Resolution Imaging Spectroradiometer (MODIS) Terra or Aqua overpass times, instead of accounting for the true observed daily variability. The mean impact of diurnal AOD variability on 24 h ADRE estimates, averaged over all AERONET sites, was rather small and it was relatively small even for the cases when AOD was chosen to correspond to the Terra or Aqua overpass time. This was true on average over all AERONET sites, while clearly there can be much stronger impact in individual sites. Examples of some selected sites demonstrated that the strongest observed AOD variability (the strongest morning afternoon contrast) does not typically result in a significant impact on 24 h ADRE. In those cases, the morning and afternoon AOD patterns are opposite and thus the impact on 24 h ADRE, when integrated over all solar zenith angles, is reduced. The most significant effect on daily ADRE was induced by AOD cycles with either maximum or minimum AOD close to local noon. In these cases, the impact on 24 h ADRE was

  7. Optical characterization of continental and biomass-burning aerosols over Bozeman, Montana: A case study of the aerosol direct effect

    NASA Astrophysics Data System (ADS)

    Nehrir, Amin R.; Repasky, Kevin S.; Reagan, John A.; Carlsten, John L.

    2011-11-01

    shown to compare favorably with regional-scale forcing calculations using MODIS-Terra and AERONET data in an effort to assess the accuracy of estimating the regional-scale aerosol direct radiative forcing effect using aerosol optical properties measured from a single rural site such as Bozeman, Montana.

  8. 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

  9. Impact of aerosol hygroscopic growth on the direct aerosol radiative effect in summer on North China Plain

    NASA Astrophysics Data System (ADS)

    Kuang, Y.; Zhao, C. S.; Tao, J. C.; Bian, Y. X.; Ma, N.

    2016-12-01

    In this paper, relative humidity (RH) profiles and their impacts on the vertical variations of aerosol optical properties and the direct aerosol radiative effect (DARE) have been investigated based on surface measurements from the Haze in China campaign and sounding data from the North China Plain. Among the profiles obtained from July to September in 2008, about half have RHs greater than 80% within the mixed layer. The vertical variations in the aerosol optical properties at ambient RH, including the extinction coefficient (σext), single scattering albedo (SSA) and asymmetry factor (g), are remarkably different from the variations in the dry aerosols and are highly dependent on the RH profiles. Increases of the aerosol optical depth and column-averaged SSA and g due to aerosol water uptake can reach up to 64%, 0.052 and 0.079, respectively. The fractional contribution to the instantaneous DARE at the top of the atmosphere due to aerosol hygroscopic growth reaches 60% in high RH profiles. DARE estimates can be significantly biased if the RH dependence of SSA or g is not considered. We suggest that if their vertical profiles or column-averaged values are absent, then the ambient values of SSA and g at the surface should be used rather than the values of SSA and g obtained from dry aerosols when estimating DAREs.

  10. CALIPSO-Inferred Aerosol Direct Radiative Effects: Bias Estimates Using Ground-Based Raman Lidars

    NASA Technical Reports Server (NTRS)

    Thorsen, Tyler; Fu, Qiang

    2015-01-01

    Observational constraints on the change in the radiative energy budget caused by the presence of aerosols, i.e. the aerosol direct radiative effect (DRE), have recently been made using observations from the Cloud- Aerosol Lidar and Infrared Pathfinder Satellite (CALIPSO). CALIPSO observations have the potential to provide improved global estimates of aerosol DRE compared to passive sensor-derived estimates due to CALIPSO's ability to perform vertically-resolved aerosol retrievals over all surface types and over cloud. In this study we estimate the uncertainties in CALIPSO-inferred aerosol DRE using multiple years of observations from the Atmospheric Radiation Measurement (ARM) program's Raman lidars (RL) at mid-latitude and tropical sites. Examined are assumptions about the ratio of extinction-to-backscatter (i.e. the lidar ratio) made by the CALIPSO retrievals, which are needed to retrieve the aerosol extinction profile. The lidar ratio is shown to introduce minimal error in the mean aerosol DRE at the top-of-atmosphere and surface. It is also shown that CALIPSO is unable to detect all radiatively-significant aerosol, resulting in an underestimate in the magnitude of the aerosol DRE by 30â€"50%. Therefore, global estimates of the aerosol DRE inferred from CALIPSO observations are likely too weak.

  11. CALIPSO-Inferred Aerosol Direct Radiative Effects: Bias Estimates Using Ground-Based Raman Lidars

    NASA Technical Reports Server (NTRS)

    Thorsen, Tyler; Fu, Qiang

    2016-01-01

    Observational constraints on the change in the radiative energy budget caused by the presence of aerosols, i.e. the aerosol direct radiative effect (DRE), have recently been made using observations from the Cloud- Aerosol Lidar and Infrared Pathfinder Satellite (CALIPSO). CALIPSO observations have the potential to provide improved global estimates of aerosol DRE compared to passive sensor-derived estimates due to CALIPSO's ability to perform vertically-resolved aerosol retrievals over all surface types and over cloud. In this study we estimate the uncertainties in CALIPSO-inferred aerosol DRE using multiple years of observations from the Atmospheric Radiation Measurement (ARM) program's Raman lidars (RL) at midlatitude and tropical sites. Examined are assumptions about the ratio of extinction-to-backscatter (i.e. the lidar ratio) made by the CALIPSO retrievals, which are needed to retrieve the aerosol extinction profile. The lidar ratio is shown to introduce minimal error in the mean aerosol DRE at the top-of-atmosphere and surface. It is also shown that CALIPSO is unable to detect all radiatively-significant aerosol, resulting in an underestimate in the magnitude of the aerosol DRE by 30-50%. Therefore, global estimates of the aerosol DRE inferred from CALIPSO observations are likely too weak.

  12. Direct Aerosol Forcing Uncertainty

    DOE Data Explorer

    Mccomiskey, Allison

    2008-01-15

    Understanding sources of uncertainty in aerosol direct radiative forcing (DRF), the difference in a given radiative flux component with and without aerosol, is essential to quantifying changes in Earth's radiation budget. We examine the uncertainty in DRF due to measurement uncertainty in the quantities on which it depends: aerosol optical depth, single scattering albedo, asymmetry parameter, solar geometry, and surface albedo. Direct radiative forcing at the top of the atmosphere and at the surface as well as sensitivities, the changes in DRF in response to unit changes in individual aerosol or surface properties, are calculated at three locations representing distinct aerosol types and radiative environments. The uncertainty in DRF associated with a given property is computed as the product of the sensitivity and typical measurement uncertainty in the respective aerosol or surface property. Sensitivity and uncertainty values permit estimation of total uncertainty in calculated DRF and identification of properties that most limit accuracy in estimating forcing. Total uncertainties in modeled local diurnally averaged forcing range from 0.2 to 1.3 W m-2 (42 to 20%) depending on location (from tropical to polar sites), solar zenith angle, surface reflectance, aerosol type, and aerosol optical depth. The largest contributor to total uncertainty in DRF is usually single scattering albedo; however decreasing measurement uncertainties for any property would increase accuracy in DRF. Comparison of two radiative transfer models suggests the contribution of modeling error is small compared to the total uncertainty although comparable to uncertainty arising from some individual properties.

  13. Potential sensitivity of photosynthesis and isoprene emission to direct radiative effects of atmospheric aerosol pollution

    NASA Astrophysics Data System (ADS)

    Strada, S.; Unger, N.

    2015-09-01

    A global Earth system model is applied to quantify the impacts of direct anthropogenic aerosol effective radiative forcing on gross primary productivity (GPP) and isoprene emission. The impacts of different pollution aerosol sources (all anthropogenic, biomass burning and non-biomass burning) are investigated by performing sensitivity experiments. On the global scale, our results show that land carbon fluxes (GPP and isoprene emission) are not sensitive to pollution aerosols, even under a global decline in surface solar radiation (direct + diffuse) by ~ 9 %. At the regional scale, plant productivity (GPP) and isoprene emission show a robust but opposite sensitivity to pollution aerosols, in regions where complex canopies dominate. In eastern North America and Europe, anthropogenic pollution aerosols (mainly from non-biomass burning sources) enhance GPP by +8-12 % on an annual average, with a stronger increase during the growing season (> 12 %). In the Amazon basin and central Africa, biomass burning aerosols increase GPP by +2-5 % on an annual average, with a peak in the Amazon basin during the dry-fire season (+5-8 %). In Europe and China, anthropogenic pollution aerosols drive a decrease in isoprene emission of -2 to -12 % on the annual average. Anthropogenic aerosols affect land carbon fluxes via different mechanisms and we suggest that the dominant mechanism varies across regions: (1) light scattering dominates in the eastern US; (2) cooling in the Amazon basin; and (3) reduction in direct radiation in Europe and China.

  14. Direct radiative effects of aerosols over South Asia from observations and modeling

    NASA Astrophysics Data System (ADS)

    Nair, Vijayakumar S.; Babu, S. Suresh; Manoj, M. R.; Moorthy, K. Krishna; Chin, Mian

    2016-10-01

    Quantitative assessment of the seasonal variations in the direct radiative effect (DRE) of composite aerosols as well as the constituent species over the Indian sub continent has been carried out using a synergy of observations from a dense network of ground based aerosol observatories and modeling based on chemical transport model simulations. Seasonal variation of aerosol constituents depict significant influence of anthropogenic aerosol sources in winter and the dominance of natural sources in spring, even though the aerosol optical depth doesn't change significantly between these two seasons. A significant increase in the surface cooling and atmospheric warming has been observed as season changes from winter (DRESUR = -28 ± 12 W m-2 and DREATM = +19.6 ± 9 W m-2) to spring (DRESUR = -33.7 ± 12 W m-2 and DREATM = +27 ± 9 W m-2). Interestingly, springtime aerosols are more absorptive in nature compared to winter and consequently the aerosol induced diabatic heating of the atmosphere goes as high as 1 K day-1 during spring, especially over eastern India. The atmospheric DRE due to dust aerosols (+14 ± 7 W m-2) during spring overwhelms that of black carbon DRE (+11.8 ± 6 W m-2) during winter. The DRE at the top of the atmosphere is mostly governed by the anthropogenic aerosols during all the seasons. The columnar aerosol loading, its anthropogenic fraction and radiative effects shows a steady increase with latitude across Indian mainland leading to a larger aerosol-induced atmospheric warming during spring than in winter.

  15. 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

  16. 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

  17. Effect of stratospheric aerosols on direct sunlight and implications for concentrating solar power.

    PubMed

    Murphy, Daniel M

    2009-04-15

    Light scattering calculations and data show that stratospheric aerosols reduce direct sunlight by about 4 W for every watt reflected to outer space. The balance becomes diffuse sunlight. One consequence of deliberate enhancement of the stratospheric aerosol layer would be a significant reduction in the efficiency of solar power generation systems using parabolic or other concentrating optics. There also would be a reduction in the effectiveness of passive solar design.

  18. Potential sensitivity of photosynthesis and isoprene emission to direct radiative effects of atmospheric aerosol pollution

    NASA Astrophysics Data System (ADS)

    Strada, Susanna; Unger, Nadine

    2016-04-01

    A global Earth system model is applied to quantify the impacts of direct anthropogenic aerosol effective radiative forcing on gross primary productivity (GPP) and isoprene emission. The impacts of different pollution aerosol sources (anthropogenic, biomass burning, and non-biomass burning) are investigated by performing sensitivity experiments. The model framework includes all known light and meteorological responses of photosynthesis, but uses fixed canopy structures and phenology. On a global scale, our results show that global land carbon fluxes (GPP and isoprene emission) are not sensitive to pollution aerosols, even under a global decline in surface solar radiation (direct + diffuse) by ˜ 9 %. At a regional scale, GPP and isoprene emission show a robust but opposite sensitivity to pollution aerosols in regions where forested canopies dominate. In eastern North America and Eurasia, anthropogenic pollution aerosols (mainly from non-biomass burning sources) enhance GPP by +5-8 % on an annual average. In the northwestern Amazon Basin and central Africa, biomass burning aerosols increase GPP by +2-5 % on an annual average, with a peak in the northwestern Amazon Basin during the dry-fire season (+5-8 %). The prevailing mechanism varies across regions: light scattering dominates in eastern North America, while a reduction in direct radiation dominates in Europe and China. Aerosol-induced GPP productivity increases in the Amazon and central Africa include an additional positive feedback from reduced canopy temperatures in response to increases in canopy conductance. In Eurasia and northeastern China, anthropogenic pollution aerosols drive a decrease in isoprene emission of -2 to -12 % on an annual average. Future research needs to incorporate the indirect effects of aerosols and possible feedbacks from dynamic carbon allocation and phenology.

  19. The direct radiative forcing effects of aerosols on the climate in California

    NASA Astrophysics Data System (ADS)

    Du, Hui

    The Weather Research and Forecast (WRF) model is used to explore the influence of aerosol direct radiative effects on regional climate of California. Aerosol data is provided by the MOZART global chemistry transport model and includes sulfate, black carbon, organic carbon, dust and sea salt. To investigate the sensitivity of aerosol radiative effects to different aerosol species and to the quantity of sulfate and dust, tests are conducted by using different combinations of aerosols and by resetting the quantity of sulfate and dust. The model results show that all the considered aerosols could have a cooling effect of one half to one degree in terms of temperature and that dust and sulfate are the most important aerosols. However, large uncertainties exist. The results suggest that the dust from MOZART is greatly overestimated over the simulation domain. The single scattering albedo (SSA) values of dust used in some global climate models are likely underestimated compared to recent studies on dust optical properties and could result in overestimating the corresponding cooling effects by approximately 0.1 degree. Large uncertainties exist in estimating the roles of different forcing factors which are causing the observed temperature change in the past century in California.

  20. Impact of aerosol vertical distribution on aerosol direct radiative effect and heating rate in the Mediterranean region

    NASA Astrophysics Data System (ADS)

    Pappas, Vasileios; Hatzianastassiou, Nikolaos; Matsoukas, Christos; Koras Carracca, Mario; Kinne, Stefan; Vardavas, Ilias

    2015-04-01

    been presented and its validity has been tested against satellite-based retrievals. A detailed spectral radiative transfer model (RTM), already used in a number of planetary and regional studies, has been used in the present study to calculate the vertically distributed aerosol direct radiative effects (DREs) and the associated aerosol heating/cooling profiles within the troposphere. Specific emphasis is given to assessment of the crucial issue of the differences between modeling the aerosol DREs using either columnar aerosol optical properties, as usually done, or vertically layered information on those properties, which is the state of the art and ideal practice. To address this problem, the following experiment has been performed: the same RTM has been used twice with the same meteorological conditions but in the first run (set1) columnar values for aerosol optical depth (AOD) have been used while using vertically distributed AOD in the second run (set2). In the second run vertically layered information for AOD is considered for 20 layers extending from the surface to 20 km a.m.s.l.. The vertical profile of AOD has been mainly based on ECHAM model. The aerosol DREs are computed at the Earth's surface, at TOA and at various levels in the atmosphere. Apart from AOD, the model also requires single-scattering albedo (SSA) and asymmetry parameter (ASY) in 18 different wavelengths, which are obtained by linear interpolation from the available wavelengths in HAC. The comparison between the obtained two sets of DRE (set1 and set2) reveal small, but notable differences which vary from one place to another. Within the atmosphere, the difference -averaged over the four seasons - ranges from -0.3 to 1.7 Wm-2 with a mean value of 0.32 Wm-2. Given the fact that the average column-integrated DREAtm values for the entire Mediterranean region based on columnar aerosol optical properties is 11.44 Wm-2, there is an average variance of 3.7 %, which locally could get to 14

  1. Modelling the direct effect of aerosols in the solar near-infrared on a planetary scale

    NASA Astrophysics Data System (ADS)

    Hatzianastassiou, N.; Matsoukas, C.; Fotiadi, A.; Stackhouse, P. W., Jr.; Koepke, P.; Pavlakis, K. G.; Vardavas, I.

    2007-06-01

    We used a spectral radiative transfer model to compute the direct radiative effect (DRE) of natural plus anthropogenic aerosols in the solar near-infrared (IR), between 0.85-10 μm, namely, their effect on the outgoing near-IR radiation at the top of atmosphere (TOA, ΔFTOA), on the atmospheric absorption of near-IR radiation (ΔFatmab) and on the surface downward and absorbed near-IR radiation (ΔFsurf, and ΔFsurfnet, respectively). The computations were performed on a global scale (over land and ocean) under all-sky conditions, using detailed spectral aerosol optical properties taken from the Global Aerosol Data Set (GADS) supplemented by realistic data for the rest of surface and atmospheric parameters. The computed aerosol DRE, averaged over the 12-year period 1984-1995 for January and July, shows that on a global mean basis aerosols produce a planetary cooling by increasing the scattered near-IR radiation back to space by 0.48 W m-2, they warm the atmosphere by 0.37 W m-2 and cool the surface by decreasing the downward and absorbed near-IR radiation at surface by 1.03 and 0.85 W m-2, respectively. The magnitude of the near-IR aerosol DRE is smaller than that of the combined ultraviolet (UV) and visible DRE, but it is still energetically important, since it contributes to the total shortwave (SW) DRE by 22-31%. The aerosol-produced near-IR surface cooling combined with the atmospheric warming, may affect the thermal dynamics of the Earth-atmosphere system, by increasing the atmospheric stability, decreasing thus cloud formation, and precipitation, especially over desertification threatened regions such as the Mediterranean basin. This, together with the fact that the sign of near-IR aerosol DRE is sometimes opposite to that of UV-visible DRE, demonstrates the importance of performing detailed spectral computations to provide estimates of the climatic role of aerosols for the Earth-atmosphere system. This was demonstrated by sensitivity tests revealing very

  2. Measurement-based estimates of direct radiative effects of absorbing aerosols above clouds

    NASA Astrophysics Data System (ADS)

    Feng, Nan; Christopher, Sundar A.

    2015-07-01

    The elevated layers of absorbing smoke aerosols from western African (e.g., Gabon and Congo) biomass burning activities have been frequently observed above low-level stratocumulus clouds off the African coast, which presents an excellent natural laboratory for studying the effects of aerosols above clouds (AAC) on regional energy balance in tropical and subtropical environments. Using spatially and temporally collocated Moderate Resolution Imaging Spectroradiometer, Ozone Monitoring Instrument (OMI), and Clouds and the Earth's Radiant Energy System data sets, the top-of-atmosphere shortwave aerosol direct shortwave radiative effects (ARE) of absorbing aerosols above low-level water clouds in the southeast Atlantic Ocean was examined in this study. The regional averaged instantaneous ARE has been estimated to be 36.7 ± 20.5 Wm-2 (regional mean ± standard deviation) along with a mean positive OMI Aerosol Index at 1.3 in August 2006 based on multisensors measurements. The highest magnitude of instantaneous ARE can even reach 138.2 Wm-2. We assess that the 660 nm cloud optical depth (COD) values of 8-12 is the critical value above (below) which aerosol absorption (scattering) effect dominates and further produces positive (negative) ARE values. The results further show that ARE values are more sensitive to aerosols above lower COD values than cases for higher COD values. This is among the first studies to provide quantitative estimates of shortwave ARE due to AAC events from an observational perspective.

  3. Direct radiative effect due to brownness in organic carbon aerosols generated from biomass combustion

    NASA Astrophysics Data System (ADS)

    Rathod, T. D.; Sahu, S. K.; Tiwari, M.; Pandit, G. G.

    2016-12-01

    We report the enhancement in the direct radiative effect due the presence of Brown carbon (BrC) as a part of organic carbon aerosols. The optical properties of organic carbon aerosols generated from pyrolytic combustion of mango tree wood (Magnifera Indica) and dung cake at different temperatures were considered. Mie codes were used to calculate absorption and scattering coefficients coupled with experimentally derived imaginary complex refractive index. The direct radiative effect (DRE) for sampled organic carbon aerosols was estimated using a wavelength dependent radiative transfer equation. The BrC DRE was estimated taking virtually non absorbing organic aerosols as reference. The BrC DRE from wood and dung cake was compared at different combustion temperatures and conditions. The BrC contributed positively to the direct top of the atmosphere radiative effect. Dung cake generated BrC aerosols were found to be strongly light absorbing as compared to BrC from wood combustion. It was noted that radiative effects of BrC from wood depended on its generation temperature and conditions. For BrC aerosols from dung cake such strong dependence was not observed. The average BrC aerosol DRE values were 1.53±0.76 W g-1 and 17.84±6.45 W g-1 for wood and dung cake respectively. The DRE contribution of BrC aerosols came mainly (67-90%) from visible light absorption though they exhibited strong absorption in shorter wavelengths of the UV-visible spectrum.

  4. Aerosol direct effect retrieval over clouds from space-borne passive hyperspectral measurements (Invited)

    NASA Astrophysics Data System (ADS)

    de Graaf, M.; Tilstra, L.; Stammes, P.

    2013-12-01

    A novel approach for the retrieval of the aerosol direct radiative effect (DRE) over clouds will be presented, which is independent of aerosol parameters estimates. The direct effect at the top of the atmosphere (TOA) of aerosols over clouds can be estimated using hyperspectral reflectance measurements from space-borne spectrometers, when the equivalent aerosol-unpolluted cloud scene reflectance spectrum is known. For smoke over clouds the cloud parameters can be estimated from the shortwave infrared (SWIR), where the absorption of the small smoke particles becomes sufficiently small. Using precomputed tables of cloud reflectance spectra, the unpolluted cloud scene spectrum can then be simulated and compared to the real measured polluted cloud scene reflectance spectrum. The UV-radiation absorption by the smoke will lead to a difference between the measured and simulated spectra, which is proportional to the aerosol DRE at TOA. Aerosol microphysical assumptions and retrievals are avoided by modeling only the aerosol-free scene spectra, all the aerosol effects are in the reflectance measurements. The method works especially well for cloud scenes, which can be simulated relatively accurately. An algorithm was developed to derive the aerosol DRE over marine clouds, using the space-borne spectrometer SCIAMACHY, which produced shortwave reflectance spectra (from 240 to 1700 nm contiguously) from 2002 till 2012. These are ideally suited to study the effect of aerosols on the shortwave spectrum. However, since aerosols in general do not have high resolution spectral features, the algorithm can be adapted to suit data from any combination of instruments that measures UV, visible and SWIR reflectances simultaneously. Examples include OMI and MODIS, flying in the A-Train constellation, and TROPOMI, on the future Sentinel 5 precursor mission, combined with NOAA's NPP VIIRS. This would produce aerosol DRE estimates with unprecedented accuracy and spatial resolution. The

  5. 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

  6. 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

  7. FY 2011 4th Quarter Metric: Estimate of Future Aerosol Direct and Indirect Effects

    SciTech Connect

    Koch, D

    2011-09-21

    The global and annual mean aerosol direct and indirect effects, relative to 1850 conditions, estimated from CESM simulations are 0.02 W m-2 and -0.39 W m-2, respectively, for emissions in year 2100 under the IPCC RCP8.5 scenario. The indirect effect is much smaller than that for 2000 emissions because of much smaller SO2 emissions in 2100; the direct effects are small due to compensation between warming by black carbon and cooling by sulfate.

  8. Direct radiative effect of aerosols based on PARASOL and OMI satellite observations

    NASA Astrophysics Data System (ADS)

    Lacagnina, Carlo; Hasekamp, Otto P.; Torres, Omar

    2017-02-01

    Accurate portrayal of the aerosol characteristics is crucial to determine aerosol contribution to the Earth's radiation budget. We employ novel satellite retrievals to make a new measurement-based estimate of the shortwave direct radiative effect of aerosols (DREA), both over land and ocean. Global satellite measurements of aerosol optical depth, single-scattering albedo (SSA), and phase function from PARASOL (Polarization and Anisotropy of Reflectances for Atmospheric Sciences coupled with Observations from a Lidar) are used in synergy with OMI (Ozone Monitoring Instrument) SSA. Aerosol information is combined with land-surface bidirectional reflectance distribution function and cloud characteristics from MODIS (Moderate Resolution Imaging Spectroradiometer) satellite products. Eventual gaps in observations are filled with the state-of-the-art global aerosol model ECHAM5-HAM2. It is found that our estimate of DREA is largely insensitive to model choice. Radiative transfer calculations show that DREA at top-of-atmosphere is -4.6 ± 1.5 W/m2 for cloud-free and -2.1 ± 0.7 W/m2 for all-sky conditions, during year 2006. These fluxes are consistent with, albeit generally less negative over ocean than, former assessments. Unlike previous studies, our estimate is constrained by retrievals of global coverage SSA, which may justify different DREA values. Remarkable consistency is found in comparison with DREA based on CERES (Clouds and the Earth's Radiant Energy System) and MODIS observations.

  9. Direct Radiative Effect of Aerosols Based on PARASOL and OMI Satellite Observations

    NASA Technical Reports Server (NTRS)

    Lacagnina, Carlo; Hasekamp, Otto P.; Torres, Omar

    2017-01-01

    Accurate portrayal of the aerosol characteristics is crucial to determine aerosol contribution to the Earth's radiation budget. We employ novel satellite retrievals to make a new measurement-based estimate of the shortwave direct radiative effect of aerosols (DREA), both over land and ocean. Global satellite measurements of aerosol optical depth, single-scattering albedo (SSA), and phase function from PARASOL (Polarization and Anisotropy of Reflectances for Atmospheric Sciences coupled with Observations from a Lidar) are used in synergy with OMI (Ozone Monitoring Instrument) SSA. Aerosol information is combined with land-surface bidirectional reflectance distribution function and cloud characteristics from MODIS (Moderate Resolution Imaging Spectroradiometer) satellite products. Eventual gaps in observations are filled with the state-of-the-art global aerosol model ECHAM5-HAM2. It is found that our estimate of DREA is largely insensitive to model choice. Radiative transfer calculations show that DREA at top-of-atmosphere is -4.6 +/- 1.5 W/sq m for cloud-free and -2.1 +/- 0.7 W/sq m for all-sky conditions, during year 2006. These fluxes are consistent with, albeit generally less negative over ocean than, former assessments. Unlike previous studies, our estimate is constrained by retrievals of global coverage SSA, which may justify different DREA values. Remarkable consistency is found in comparison with DREA based on CERES (Clouds and the Earth's Radiant Energy System) and MODIS observations.

  10. Implications of the Temporal Resolution of Fire Emissions on Direct and Indirect Aerosol Effects

    NASA Astrophysics Data System (ADS)

    Darmenov, A.; Barahona, D.; Kim, K. M.; da Silva, A.; Colarco, P. R.; Govindaraju, R.

    2014-12-01

    Biomass burning is an important source of particulates and trace gases and a major element of the terrestrial carbon cycle. Well constrained emissions from open vegetation fires in both time and space are needed to model direct and indirect effect of biomass burning aerosols, homogeneous and heterogeneous chemistry in the atmosphere and perform credible integrated earth system analysis, climate and air pollution studies. However representing fires in regional and global numerical models is challenging because of the subgrid scales at which fire processes operate. An example of apparent discrepancy in scales is the use of monthly- or seasonal-mean fire emissions which given the stochastic nature of fires means that at certain spatial scales the temporal behavior of emissions becomes influenced by individual fire events and becomes more variable. The present study aims at investigating the impact of monthly-mean fire emissions on direct and indirect aerosol effects. Key element of our work is the use of fire radiative power (FRP) based emissions and a global fully interactive cloud-aerosol-radiation modeling system. We used the Goddard Earth Observing System Model, Version 5 (GEOS-5) with two moment cloud microphysics and explicit cloud droplet activation and ice nucleation. GEOS-5 is coupled with an online version of the Goddard Chemistry Aerosol Radiation and Transport (GOCART) model. Biomass burning emissions used in this study are from the Quick Fire Emission Dataset (QFED) available daily at up to 0.1 degrees horizontal resolution. We performed experiments with daily-mean and monthly-mean QFED emissions at two degree horizontal resolutions and report differences in aerosol burden and radiative forcing, for example we found that regional differences of clear-sky aerosol direct radiative effect at the surface and at the top of the atmosphere in MAM and JJA can be as high as 4 Wm-2 and 3 Wm-2, respectively.

  11. Estimating the direct aerosol radiative effect over China using multi-sensor satellite remote sensing measurements

    NASA Astrophysics Data System (ADS)

    Sundström, Anu-Maija; Arola, Antti; Kolmonen, Pekka; de Leeuw, Gerrit

    2013-04-01

    The quantification of aerosol radiative effects is complex and large uncertainties still exist, mainly due to the high spatial and temporal variation of the aerosol concentration and mass as well as their relatively short lifetime in the atmosphere. In this work a multi-sensor satellite based approach is studied for defining the direct short wave aerosol radiative effect (ADRE) over China. ADRE at the top of the atmosphere (TOA) is defined as the difference between the net solar flux with (F) and without (F0) aerosols. The negative values of ADRE correspond to increased outgoing radiation and planetary cooling, whereas positive values correspond to decreased outgoing radiation at TOA and increased atmospheric warming. To derive instantaneous ADRE from the satellite observations, the challenge is to estimate the value for F0. In this work F0 is derived using the colocated observations of CERES (Clouds and the Earth's Radian Energy System) short wave broad band TOA-flux and MODIS (Moderate Imaging Spectroradiometer) aerosol optical depth (AOD). Assuming that aerosol type does not change systematically within a 0.5 deg. grid cell over a month, a linear relationship is established between the TOA-flux and AOD when AOD < 2.0. Using the linear fit an estimate for F0 can be obtained and F is the monthly mean of CERES observations. However, there are several other parameters affecting the observed TOA flux than the aerosol loading and aerosol type, such as solar zenith angle, water vapour, land surface albedo and Earth-Sun distance. Changes in these parameters within a grid cell over a month inflect the correlation. To minimize the effect of zenith angle, water vapour, and Earth-Sun distance the CERES fluxes are normalized before the linear fitting using reference fluxes calculated with a radiative transfer code (Libradtran). The normalization, especially to a fixed zenith angle increases the correlation between TOA flux and AOD significantly. For a comparison theF0 is

  12. Impact of aerosol direct effect on East Asian air quality during the EAST-AIRE campaign

    NASA Astrophysics Data System (ADS)

    Wang, Jing; Allen, Dale J.; Pickering, Kenneth E.; Li, Zhanqing; He, Hao

    2016-06-01

    WRF-Chem simulations were performed for the March 2005 East Asian Studies of Tropospheric Aerosols: an International Regional Experiment (EAST-AIRE) Intensive Observation Campaign (IOC) to investigate the direct effects of aerosols on surface radiation and air quality. Domain-wide, WRF-Chem showed a decrease of 20 W/m2 in surface shortwave (SW) radiation due to the aerosol direct effect (ADE), consistent with observational studies. The ADE caused 24 h surface PM2.5 (particulate matter with diameter < 2.5 µm) concentrations to increase in eastern China (4.4%), southern China (10%), western China (2.3%), and the Sichuan Basin (9.6%), due to different aerosol compositions in these four regions. Conversely, surface 1 h maximum ozone was reduced by 2.3% domain-wide and up to 12% in eastern China because less radiation reached the surface. We also investigated the impact of reducing SO2 and black carbon (BC) emissions by 80% on aerosol amounts via two sensitivity simulations. Reducing SO2 decreased surface PM2.5 concentrations in the Sichuan Basin and southern China by 5.4% and decreased ozone by up to 6 ppbv in the Sichuan Basin and Southern China. Reducing BC emissions decreased PM2.5 by 3% in eastern China and the Sichuan Basin but increased surface ozone by up to 3.6 ppbv in eastern China and the Sichuan Basin. This study indicates that the benefits of reducing PM2.5 associated with reducing absorbing aerosols may be partially offset by increases in ozone at least for a scenario when NOx and VOC emissions are unchanged.

  13. Radiative forcing of the direct aerosol effect from AeroCom Phase II simulations

    NASA Astrophysics Data System (ADS)

    Myhre, G.; Samset, B. H.; Schulz, M.; Balkanski, Y.; Bauer, S.; Berntsen, T. K.; Bian, H.; Bellouin, N.; Chin, M.; Diehl, T.; Easter, R. C.; Feichter, J.; Ghan, S. J.; Hauglustaine, D.; Iversen, T.; Kinne, S.; Kirkevåg, A.; Lamarque, J.-F.; Lin, G.; Liu, X.; Lund, M. T.; Luo, G.; Ma, X.; van Noije, T.; Penner, J. E.; Rasch, P. J.; Ruiz, A.; Seland, Ø.; Skeie, R. B.; Stier, P.; Takemura, T.; Tsigaridis, K.; Wang, P.; Wang, Z.; Xu, L.; Yu, H.; Yu, F.; Yoon, J.-H.; Zhang, K.; Zhang, H.; Zhou, C.

    2013-02-01

    We report on the AeroCom Phase II direct aerosol effect (DAE) experiment where 16 detailed global aerosol models have been used to simulate the changes in the aerosol distribution over the industrial era. All 16 models have estimated the radiative forcing (RF) of the anthropogenic DAE, and have taken into account anthropogenic sulphate, black carbon (BC) and organic aerosols (OA) from fossil fuel, biofuel, and biomass burning emissions. In addition several models have simulated the DAE of anthropogenic nitrate and anthropogenic influenced secondary organic aerosols (SOA). The model simulated all-sky RF of the DAE from total anthropogenic aerosols has a range from -0.58 to -0.02 Wm-2, with a mean of -0.27 Wm-2 for the 16 models. Several models did not include nitrate or SOA and modifying the estimate by accounting for this with information from the other AeroCom models reduces the range and slightly strengthens the mean. Modifying the model estimates for missing aerosol components and for the time period 1750 to 2010 results in a mean RF for the DAE of -0.35 Wm-2. Compared to AeroCom Phase I (Schulz et al., 2006) we find very similar spreads in both total DAE and aerosol component RF. However, the RF of the total DAE is stronger negative and RF from BC from fossil fuel and biofuel emissions are stronger positive in the present study than in the previous AeroCom study. We find a tendency for models having a strong (positive) BC RF to also have strong (negative) sulphate or OA RF. This relationship leads to smaller uncertainty in the total RF of the DAE compared to the RF of the sum of the individual aerosol components. The spread in results for the individual aerosol components is substantial, and can be divided into diversities in burden, mass extinction coefficient (MEC), and normalized RF with respect to AOD. We find that these three factors give similar contributions to the spread in results.

  14. Radiative forcing of the direct aerosol effect from AeroCom Phase II simulations

    NASA Astrophysics Data System (ADS)

    Myhre, G.; Samset, B. H.; Schulz, M.; Balkanski, Y.; Bauer, S.; Berntsen, T. K.; Bian, H.; Bellouin, N.; Chin, M.; Diehl, T.; Easter, R. C.; Feichter, J.; Ghan, S. J.; Hauglustaine, D.; Iversen, T.; Kinne, S.; Kirkevåg, A.; Lamarque, J.-F.; Lin, G.; Liu, X.; Luo, G.; Ma, X.; Penner, J. E.; Rasch, P. J.; Seland, Ø.; Skeie, R. B.; Stier, P.; Takemura, T.; Tsigaridis, K.; Wang, Z.; Xu, L.; Yu, H.; Yu, F.; Yoon, J.-H.; Zhang, K.; Zhang, H.; Zhou, C.

    2012-08-01

    We report on the AeroCom Phase II direct aerosol effect (DAE) experiment where 15 detailed global aerosol models have been used to simulate the changes in the aerosol distribution over the industrial era. All 15 models have estimated the radiative forcing (RF) of the anthropogenic DAE, and have taken into account anthropogenic sulphate, black carbon (BC) and organic aerosols (OA) from fossil fuel, biofuel, and biomass burning emissions. In addition several models have simulated the DAE of anthropogenic nitrate and anthropogenic influenced secondary organic aerosols (SOA). The model simulated all-sky RF of the DAE from total anthropogenic aerosols has a range from -0.58 to -0.02 W m-2, with a mean of -0.30 W m-2 for the 15 models. Several models did not include nitrate or SOA and modifying the estimate by accounting for this with information from the other AeroCom models reduces the range and slightly strengthens the mean. Modifying the model estimates for missing aerosol components and for the time period 1750 to 2010 results in a mean RF for the DAE of -0.39 W m-2. Compared to AeroCom Phase I (Schulz et al., 2006) we find very similar spreads in both total DAE and aerosol component RF. However, the RF of the total DAE is stronger negative and RF from BC from fossil fuel and biofuel emissions are stronger positive in the present study than in the previous AeroCom study. We find a tendency for models having a strong (positive) BC RF to also have strong (negative) sulphate or OA RF. This relationship leads to smaller uncertainty in the total RF of the DAE compared to the RF of the sum of the individual aerosol components. The spread in results for the individual aerosol components is substantial, and can be divided into diversities in burden, mass extinction coefficient (MEC), and normalized RF with respect to AOD. We find that these three factors give similar contributions to the spread in results.

  15. Radiative Forcing of the Direct Aerosol Effect from AeroCom Phase II Simulations

    NASA Technical Reports Server (NTRS)

    Myhre, G.; Samset, B. H.; Schulz, M.; Balkanski, Y.; Bauer, S.; Berntsen, T. K.; Bian, H.; Bellouin, N.; Chin, M.; Diehl, T.; Easter, R. C.; Feichter, J.; Ghan, S. J.; Hauglustaine, D.; Iversen, T.; Kinne, S.; Kirkevag, A.; Lamarque, J.-F.; Lin, G.; Liu, X.; Lund, M. T.; Luo, G.; Ma, X.; vanNoije, T.; Penner, J. E.; Rasch, P. J.; Ruiz, A.; Seland, O.; Skeie, R. B.; Stier, P.; Takemura, T.; Tsigaridis, K.; Wang, P.; Wang, Z.; Xu, L.; Yu, H.; Yu, F.; Yoon, J. -H.; Zhang, K.; Zhang, H.; Zhou, C.

    2013-01-01

    We report on the AeroCom Phase II direct aerosol effect (DAE) experiment where 16 detailed global aerosol models have been used to simulate the changes in the aerosol distribution over the industrial era. All 16 models have estimated the radiative forcing (RF) of the anthropogenic DAE, and have taken into account anthropogenic sulphate, black carbon (BC) and organic aerosols (OA) from fossil fuel, biofuel, and biomass burning emissions. In addition several models have simulated the DAE of anthropogenic nitrate and anthropogenic influenced secondary organic aerosols (SOA). The model simulated all-sky RF of the DAE from total anthropogenic aerosols has a range from -0.58 to -0.02 W m(sup-2), with a mean of -0.27 W m(sup-2 for the 16 models. Several models did not include nitrate or SOA and modifying the estimate by accounting for this with information slightly strengthens the mean. Modifying the model estimates for missing aerosol components and for the time period 1750 to 2010 results in a mean RF for the DAE of -0.35 W m(sup-2). Compared to AeroCom Phase I (Schulz et al., 2006) we find very similar spreads in both total DAE and aerosol component RF. However, the RF of the total DAE is stronger negative and RF from BC from fossil fuel and biofuel emissions are stronger positive in the present study than in the previous AeroCom study.We find a tendency for models having a strong (positive) BC RF to also have strong (negative) sulphate or OA RF. This relationship leads to smaller uncertainty in the total RF of the DAE compared to the RF of the sum of the individual aerosol components. The spread in results for the individual aerosol components is substantial, and can be divided into diversities in burden, mass extinction coefficient (MEC), and normalized RF with respect to AOD. We find that these three factors give similar contributions to the spread in results

  16. Radiative forcing of the direct aerosol effect from AeroCom Phase II simulations

    SciTech Connect

    Myhre, G.; Samset, B. H.; Schulz, M.; Balkanski, Y.; Bauer, S.; Berntsen, T. K.; Bian, H.; Bellouin, N.; Chin, M.; Diehl, T.; Easter, R. C.; Feichter, J.; Ghan, S. J.; Hauglustaine, D.; Iversen, T.; Kinne, S.; Kirkevåg, A.; Lamarque, J. -F.; Lin, G.; Liu, X.; Lund, M. T.; Luo, G.; Ma, X.; van Noije, T.; Penner, J. E.; Rasch, P. J.; Ruiz, A.; Seland, Ø.; Skeie, R. B.; Stier, P.; Takemura, T.; Tsigaridis, K.; Wang, P.; Wang, Z.; Xu, L.; Yu, H.; Yu, F.; Yoon, J. -H.; Zhang, K.; Zhang, H.; Zhou, C.

    2013-01-01

    We report on the AeroCom Phase II direct aerosol effect (DAE) experiment where 16 detailed global aerosol models have been used to simulate the changes in the aerosol distribution over the industrial era. All 16 models have estimated the radiative forcing (RF) of the anthropogenic DAE, and have taken into account anthropogenic sulphate, black carbon (BC) and organic aerosols (OA) from fossil fuel, biofuel, and biomass burning emissions. In addition several models have simulated the DAE of anthropogenic nitrate and anthropogenic influenced secondary organic aerosols (SOA). The model simulated all-sky RF of the DAE from total anthropogenic aerosols has a range from -0.58 to -0.02 Wm-2, with a mean of -0.27 Wm-2 for the 16 models. Several models did not include nitrate or SOA and modifying the estimate by accounting for this with information from the other AeroCom models reduces the range and slightly strengthens the mean. Modifying the model estimates for missing aerosol components and for the time period 1750 to 2010 results in a mean RF for the DAE of -0.35 Wm-2. Compared to AeroCom Phase I (Schulz et al., 2006) we find very similar spreads in both total DAE and aerosol component RF. However, the RF of the total DAE is stronger negative and RF from BC from fossil fuel and biofuel emissions are stronger positive in the present study than in the previous AeroCom study. We find a tendency for models having a strong (positive) BC RF to also have strong (negative) sulphate or OA RF. This relationship leads to smaller uncertainty in the total RF of the DAE compared to the RF of the sum of the individual aerosol components. The spread in results for the individual aerosol components is substantial, and can be divided into diversities in burden, mass extinction coefficient (MEC), and normalized RF with respect to AOD. We find that these three factors give similar contributions to the spread in results.

  17. Southeast Atlantic Ocean aerosol direct radiative effects over clouds: Comparison of observations and simulations

    NASA Astrophysics Data System (ADS)

    de Graaf, M.; Haywood, J.; Bellouin, N.; Tilstra, L. G.; Stammes, P.

    2017-02-01

    Absorbing aerosols exert a warming or a cooling effect on the Earth's system, depending on the circumstances. The direct radiative effect (DRE) of absorbing aerosols is negative (cooling) at the top-of-the-atmosphere (TOA) over a dark surface like the ocean, as the aerosols increase the planetary albedo, but it is positive (warming) over bright backgrounds like clouds. Furthermore, radiation absorption by aerosols heat the atmosphere locally, and, through rapid adjustments of the atmospheric column and cloud dynamics, the net effect can be amplified considerably. We developed a technique to study the absorption of radiation of smoke over low lying clouds using satellite spectrometry. The TOA DRE of smoke over clouds is large and positive over the southeast Atlantic Ocean off the west coast of Africa, which can be explained by the large decrease of reflected radiation by a polluted cloud, especially in the UV. However, general circulation models (GCMs) fail to reproduce these strong positive DRE, and in general GCMs disagree on the magnitude and even sign of the aerosol DRE in the southeast Atlantic region. Our satellite-derived DRE measurements show clear seasonal and inter-annual variations, consistent with other satellite measurements, which are not reproduced by GCMs. A comparison with model results showed discrepancies with the Ångström exponent of the smoke aerosols, which is larger than assumed in simulations, and a sensitivity to emission scenarios. However, this was not enough to explain the discrepancies, and we suspect that the modeling of cloud distributions and microphysics will have the necessary larger impact on DRE that will explain the differences between observations and modeling.

  18. Modelling the direct effect of aerosols in the solar near-infrared on a planetary scale

    NASA Astrophysics Data System (ADS)

    Hatzianastassiou, N.; Matsoukas, C.; Fotiadi, A.; Drakakis, E.; Stackhouse, P. W., Jr.; Koepke, P.; Pavlakis, K. G.; Hatzidimitriou, D.; Vardavas, I.

    2006-09-01

    We used a spectral radiative transfer model to compute the direct radiative effect (DRE) of natural plus anthropogenic aerosols in the solar near-infrared (IR), between 0.85-10 µm, namely, their effect on the outgoing near-IR radiation at the top of atmosphere (TOA, ΔFTOA), on the atmospheric absorption of near-IR radiation (ΔFatmab) and on the surface downward and absorbed near-IR radiation (ΔFsurf, and ΔFsurfnet, respectively). The computations were performed on a global scale (over land and ocean) under all-sky conditions, using spectral aerosol optical properties taken from the Global Aerosol Data Set (GADS) supplemented by realistic data for the rest of surface and atmospheric parameters. The computed aerosol DRE, averaged over the 12-year period 1984-1995 for January and July, shows that aerosols produce a planetary cooling by increasing the scattered near-IR radiation back to space (by up to 6 Wm-2), they warm the atmosphere (by up to 7 Wm-2) and cool the surface (by up to 12 Wm-2). However, they can also slightly warm the Earth-atmosphere system or cool the atmosphere (by less than 1 Wm-2) over limited areas. The magnitude of the near-IR aerosol DRE is smaller than that of the combined ultraviolet (UV) and visible DRE, but it is still energetically important, since it contributes to the total shortwave (SW) DRE by 22-31%. On a global mean basis, the DREs ΔFTOA, ΔFatmab, ΔFsurf, and ΔFsurfnet are equal to about 0.48, 0.37, -1.03 and -0.85 Wm-2, i.e. their magnitude is similar to that of climate forcing associated with increasing concentrations of greenhouse gases. The aerosol induced near-IR surface cooling combined with the atmospheric warming, affects the thermal dynamics of the Earth-atmosphere system, by increasing the atmospheric stability, decreasing thus cloud formation, and precipitation, especially over desertification threatened regions such as the Mediterranean basin. This, together with the fact that the sign of near-IR aerosol DRE is

  19. 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.

  20. "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...

  1. “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...

  2. Direct effect of aerosol optical properties on global dimming and brightening

    NASA Astrophysics Data System (ADS)

    Kudo, R.; Uchiyama, A.

    2011-12-01

    Surface solar radiation observed at numerous locations has decreased from the 1960s to the 1980s (Global dimming), thereafter increased (Global brightening). The dimming and brightening is considered to be due to the changes in both clouds and aerosols. Aerosols have a direct impact on the surface solar radiation by scattering and absorption. The impact is determined by three parameters: optical depth (AOD), single scattering albedo (SSA), and asymmetry factor, but the effect of asymmetry factor is rather smaller than the others. Therefore, the long-term changes in AOD and SSA are necessary to evaluate the aerosol impact on the global dimming and brightening. We have developed the method to estimate AOD and SSA from the hourly accumulated direct and diffuse irradiances measured by the ground-based broadband radiometers. In the estimation, the real part of the refractive index is fixed, and the size distribution is defined by the Junge distribution with a fixed shaping constant. Using the developed method, the measurements from 1975 to 2008 at 14 sites in Japan were analyzed. Consequently, a decrease of AOD by 0.02 and an increase of SSA by 0.2 during the period were seen. The surface solar radiation under the clear sky conditions, which was calculated from the estimated aerosol optical properties, was increased by 5% due to the changes in AOD and SSA; the influence of SSA was dominant. We also investigate the cloud impact on the surface solar radiation which was simply defined as the difference between the surface solar radiation under the cloudy sky conditions and under the clear sky conditions; the cloud impact had no statistically significant trends. The brightening in Japan may be due to the changes in aerosol optical properties, especially SSA. Our developed method can be applied to measurements at other sites around the world and would be helpful to understand the causes of the global dimming and brightening.

  3. Impact of Aerosol Direct Effect on East Asian Air Quality During the EAST-AIRE Campaign

    NASA Astrophysics Data System (ADS)

    Wang, J.; Allen, D. J.; Pickering, K. E.; Li, Z.

    2015-12-01

    Three WRF-Chem simulations were conducted for East Asia region during March 2005 East Asian Studies of Tropospheric Aerosols: an International Regional Experiment (EAST-AIRE) Intensive Observation Campaign (IOC) period to investigate the direct effects of aerosols on surface radiation and air quality. WRF-Chem captured the temporal and spatial variations of meteorological fields, trace gases, and aerosol loadings. Surface shortwave radiation changes due to the aerosol direct effect (ADE) were calculated and compared with data from six World Radiation Data Center (WRDC) stations. The comparison indicated that WRF-Chem can simulate the surface short wave radiation moderately well, with temporal correlations between 0.4 and 0.7, and high biases between 9 to 120 W/m2. Domain-wide, WRF-Chem showed a decrease of 22 W/m2 in surface SW radiation due to the aerosol direct effect, consistent with observational studies. The ADE demonstrates diverse influences on air quality in East Asian. For example, the surface concentration of PM2.5 increases in eastern China (~11.1%) due to ADE, but decreases in central China (-7.3%), western China (-8.8%), and Sichuan Basin (-4%). Surface 1-hour maximum ozone is reduced by 2.3%, owing to less radiation reaching the surface due to the ADE. Since PM2.5 pollution raises serious public concern in China, regulations that control the emissions of PM2.5 and its precursors have been implemented. We investigate the impact of reducing two different types of aerosols, sulfate (scattering) and black carbon (absorbing), by cutting 80% of SO2 and black carbon (BC) emissions in two sensitivity simulations. We found that reducing SO2 emissions results in the decline of PM2.5 as much as 16mg/m3 in eastern China, and 20mg/m3 in the Sichuan Basin. Reducing the BC emissions by the same percentage causes the PM2.5 to decrease as much as 40mg/m3 in eastern China, and 25mg/m3 in the Sichuan Basin. The monthly averaged surface 1-hour maximum ozone increases 3

  4. 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.

  5. Quantification of the aerosol direct radiative effect from smoke over clouds using passive space-borne spectrometry

    NASA Astrophysics Data System (ADS)

    de Graaf, M.; Stammes, P.; Tilstra, L. G.

    2013-05-01

    The solar radiative absorption by smoke layers above clouds is quantified, using the unique broad spectral range of the space-borne spectrometer Scanning Imaging Absorption Spectrometer for Atmospheric Chartography (SCIAMACHY) from the ultraviolet (UV) to the shortwave infrared (SWIR). Aerosol radiative effects in the UV are separated from cloud radiative effects in the shortwave infrared (SWIR). In the UV, aerosol absorption from smoke is strong, creating a strong signal in the measured reflectance. In the SWIR, absorbing and scattering effects from smoke are negligible, allowing the retrieval of cloud parameters from the measured spectrum using existing retrieval techniques. The spectral signature of the cloud can be modelled using a radiative transfer model (RTM) and the cloud parameters retrieved in the SWIR. In this way, the aerosol effects can be determined from the measured aerosol-polluted cloud shortwave spectrum and the modelled aerosol-unpolluted cloud shortwave spectrum. This can be used to derive the aerosol direct radiative effect (DRE) over marine clouds, independent of aerosol parameter retrievals, significantly improving the current accuracy of aerosol DRE estimates. Only cloud parameters are needed to model the aerosolunpolluted cloud reflectance, while the effects of the aerosol absorption are in the aerosol-polluted cloud reflectance measurements. In this paper we present a case study of the above method using SCIAMACHY data over the South Atlantic Ocean west of Africa on 13 August 2006, when a huge plume of smoke was present over persistent cloud fields. The aerosol DRE over clouds was as high as 128 ± 8 Wm-2 for this case, while the aerosol DRE over clouds averaged through August 2006 was found to be 23 ± 8 Wm-2 with a mean variation over the region in this month of 22 Wm-2.

  6. 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.

  7. Understanding the direct radiative effect of dust aerosols on transport pathways using the NASA GEOS-5 AGCM

    NASA Astrophysics Data System (ADS)

    Nowottnick, E. P.; Colarco, P. R.; Lau, W. K.; Kim, K.

    2012-12-01

    African dust aerosols are transported across the Atlantic Ocean to the Caribbean by the easterly trade winds.While in transport, dust aerosols interact with the Earth system in various ways, ranging from influencing the local radiation balance to serving as a nutrient for tropical ecosystems.However, our current understanding of these processes is incomplete and serves as a source of uncertainty in Earth system modeling.Here, we focus on understanding the direct radiative impacts of African dust aerosols on the atmosphere using the NASA GEOS-5 atmospheric general circulation model that simulates aerosols with an online version of the GOCART model. For this study, we compare a high resolution GEOS-5 climate simulation where aerosols have been radiatively coupled to the atmosphere to one where aerosols are treated as passive tracers for June - September, 2009. Utilizing streamfunction and velocity potentials of the simulated dust mass flux, we isolate differences in dust transport pathways caused by the direct radiative effect of dust by comparing the rotational and divergent components of the dust flow in the horizontal and vertical on various timescales.Additionally, we pay special attention to the influence of dust aerosols on African Easterly Jet (AEJ) position and strength, as well as temperature profiles, cloudiness, and precipitation to gain further insight into the direct radiative effect of dust aerosols on the atmosphere

  8. The direct effect of aerosols on solar radiation over the broader Mediterranean basin

    NASA Astrophysics Data System (ADS)

    Papadimas, C. D.; Hatzianastassiou, N.; Matsoukas, C.; Kanakidou, M.; Mihalopoulos, N.; Vardavas, I.

    2011-11-01

    For the first time, the direct radiative effect (DRE) of aerosols on solar radiation is computed over the entire Mediterranean basin, one of the most climatically sensitive world regions, by using a deterministic spectral radiation transfer model (RTM). The DRE effects on the outgoing shortwave radiation at the top of atmosphere (TOA), DRETOA, on the absorption of solar radiation in the atmospheric column, DREatm, and on the downward and absorbed surface solar radiation (SSR), DREsurf and DREnetsurf, respectively, are computed separately. The model uses input data for the period 2000-2007 for various surface and atmospheric parameters, taken from satellite (International Satellite Cloud Climatology Project, ISCCP-D2), Global Reanalysis projects (National Centers for Environmental Prediction - National Center for Atmospheric Research, NCEP/NCAR), and other global databases. The spectral aerosol optical properties (aerosol optical depth, AOD, asymmetry parameter, gaer and single scattering albedo, ωaer), are taken from the MODerate resolution Imaging Spectroradiometer (MODIS) of NASA (National Aeronautics and Space Administration) and they are Supplemented by the Global Aerosol Data Set (GADS). The model SSR fluxes have been successfully validated against measurements from 80 surface stations of the Global Energy Balance Archive (GEBA) covering the period 2000-2007. A planetary cooling is found above the Mediterranean on an annual basis (regional mean DRETOA = -2.4 Wm-2). Though planetary cooling is found over most of the region, up to -7 Wm-2, large positive DRETOA values (up to +25 Wm-2) are found over North Africa, indicating a strong planetary warming, as well as over the Alps (+0.5 Wm-2). Aerosols are found to increase the absorption of solar radiation in the atmospheric column over the region (DREatm = +11.1 Wm-2) and to decrease SSR (DREsurf = -16.5 Wm-2 and DREnetsurf -13.5 Wm-2) inducing thus significant atmospheric warming and surface radiative cooling

  9. 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.

  10. 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.

  11. 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.

  12. QUantifying the Aerosol Direct and Indirect Effect over Eastern Mediterranean from Satellites (QUADIEEMS): Satellite, model and reanalysis data synergy

    NASA Astrophysics Data System (ADS)

    Georgoulias, A.; Zanis, P.; Poeschl, U.; Kourtidis, K.; Alexandri, G.; Dogras, C.; Marinou, E.; Amiridis, V.

    2013-12-01

    The research implemented within the QUADIEEMS project is presented here. Satellite data from five sensors (MODIS aboard EOS TERRA, MODIS aboard EOS AQUA, TOMS aboard Earth Probe, OMI aboard EOS AURA and CALIOP aboard CALIPSO) are combined with meteorological data from ECMWF ERA-interim reanalysis, aerosol data from a global chemical-aerosol-transport model (GOCART) and MACC reanalysis as well as simulation results from a regional climate model (RegCM4) coupled with a simplified aerosol scheme. QUADIEEMS focuses on Eastern Mediterranean [30N-45N, 17.5E-37.5E]. Various sources, like industry and transport, occasional Saharan dust intrusions, sea spray and agricultural fires in Southeastern and Eastern Europe as well as occasional fire events in the region, create an ideal environment for the investigation of the direct and indirect effects of various aerosol types. The acquired data were spatially homogenized resulting in a novel satellite-model-reanalysis high resolution (0.1x0.1 degree) dataset of aerosol and cloud optical properties. The relative contribution of marine, dust and anthropogenic aerosols to the total aerosol optical depth (AOD550) is quantified combining different parameters from our high resolution dataset. The same procedure is repeated at a moderate resolution (1.0x1.0 degree). Within QUADIEEMS, decadal REGCM4/aerosol regional climate model simulations are implemented for the greater European region at a resolution of 50 km. We evaluate the ability of REGCM4 to simulate AOD550 patterns. For different sub-regions of Eastern Mediterranean, the aerosol-cloud relationships are examined. The same procedure is repeated also taking into account the relative position of aerosol and cloud layers as defined by CALIPSO observations. Results and data from the first four components of the project are used in satellite-based parameterizations to quantify the direct and indirect (first) radiative effect of the different aerosol types at a resolution of 0.1x0

  13. Combined multispectral/hyperspectral remote sensing of tropospheric aerosols for quantification of their direct radiative effect

    NASA Astrophysics Data System (ADS)

    McGarragh, Gregory R.

    Scattering and absorption of solar radiation by aerosols in the atmosphere has a direct radiative effect on the climate of the Earth. Unfortunately, according to the IPCC the uncertainties in aerosol properties and their effect on the climate system represent one of the largest uncertainties in climate change research. Related to aerosols, one of the largest uncertainties is the fraction of the incident radiation that is scattered rather than absorbed, or their single scattering albedo. In fact, differences in single scattering albedo have a significant impact on the magnitude of the cooling effect of aerosols (opposite to that of greenhouse gasses) which can even have a warming effect for strongly absorbing aerosols. Satellites provide a unique opportunity to measure aerosol properties on a global scale. Traditional approaches use multispectral measurements of intensity at a single view angle to retrieve at most two aerosol parameters over land but it is being realized that more detail is required for accurate quantification of the direct effect of aerosols, in particular its anthropogenic component, and therefore more measurement information is required. One approach to more advanced measurements is to use not only intensity measurements but also polarimetric measurements and to use multiple view angles. In this work we explore another alternative: the use of hyperspectral measurements in molecular absorption bands. Our study can be divided into three stages the first of which is the development of a fast radiative transfer model for rapid simulation of measurements. Our approach is matrix operator based and uses the Pade approximation for the matrix exponential to evaluate the homogeneous solution. It is shown that the method is two to four times faster than the standard and efficient discrete ordinate technique and is accurate to the 6th decimal place. The second part of our study forms the core and is divided into two chapters the first of which is a rigorous

  14. Can Aerosol Direct Radiative Effects Account for Analysis Increments of Temperature in the Tropical Atlantic?

    NASA Technical Reports Server (NTRS)

    da Silva, Arlindo M.; Alpert, Pinhas

    2016-01-01

    In the late 1990's, prior to the launch of the Terra satellite, atmospheric general circulation models (GCMs) did not include aerosol processes because aerosols were not properly monitored on a global scale and their spatial distributions were not known well enough for their incorporation in operational GCMs. At the time of the first GEOS Reanalysis (Schubert et al. 1993), long time series of analysis increments (the corrections to the atmospheric state by all available meteorological observations) became readily available, enabling detailed analysis of the GEOS-1 errors on a global scale. Such analysis revealed that temperature biases were particularly pronounced in the Tropical Atlantic region, with patterns depicting a remarkable similarity to dust plumes emanating from the African continent as evidenced by TOMS aerosol index maps. Yoram Kaufman was instrumental encouraging us to pursue this issue further, resulting in the study reported in Alpert et al. (1998) where we attempted to assess aerosol forcing by studying the errors of a the GEOS-1 GCM without aerosol physics within a data assimilation system. Based on this analysis, Alpert et al. (1998) put forward that dust aerosols are an important source of inaccuracies in numerical weather-prediction models in the Tropical Atlantic region, although a direct verification of this hypothesis was not possible back then. Nearly 20 years later, numerical prediction models have increased in resolution and complexity of physical parameterizations, including the representation of aerosols and their interactions with the circulation. Moreover, with the advent of NASA's EOS program and subsequent satellites, atmospheric aerosols are now monitored globally on a routine basis, and their assimilation in global models are becoming well established. In this talk we will reexamine the Alpert et al. (1998) hypothesis using the most recent version of the GEOS-5 Data Assimilation System with assimilation of aerosols. We will

  15. A multi-satellite analysis of the direct radiative effects of absorbing aerosols above clouds

    NASA Astrophysics Data System (ADS)

    Chang, Y. Y.; Christopher, S. A.

    2015-12-01

    Radiative effects of absorbing aerosols above liquid water clouds in the southeast Atlantic as a function of fire sources are investigated using A-Train data coupled with the Visible Infrared Imaging Radiometer Suite (VIIRS) onboard Suomi National Polar-orbiting Partnership (Suomi NPP). Both the VIIRS Active Fire product and the Aqua Moderate Resolution Imaging Spectroradiometer (MODIS) Thermal Anomalies product (MYD14) are used to identify the biomass burning fire origin in southern Africa. The Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP) are used to assess the aerosol type, aerosol altitude, and cloud altitude. We use back trajectory information, wind data, and the Fire Locating and Modeling of Burning Emissions (FLAMBE) product to infer the transportation of aerosols from the fire source to the CALIOP swath in the southeast Atlantic during austral winter.

  16. 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

  17. 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.

  18. The interplay between assumed morphology and the direct radiative effect of light-absorbing organic aerosol

    NASA Astrophysics Data System (ADS)

    Saleh, Rawad; Adams, Peter J.; Donahue, Neil M.; Robinson, Allen L.

    2016-08-01

    Mie theory is widely employed in aerosol top-of-the-atmosphere direct radiative effect (DRE) calculations and to retrieve the absorptivity of light-absorbing organic aerosol (OA) from measurements. However, when OA is internally mixed with black carbon, it may exhibit complex morphologies whose optical behavior is imperfectly predicted by Mie theory, introducing bias in the retrieved absorptivities. We performed numerical experiments and global radiative transfer modeling (RTM) to investigate the effect of this bias on the calculated absorption and thus the DRE. We show that using true OA absorptivity, retrieved with a realistic representation of the complex morphology, leads to significant errors in DRE when the RTM employs the simplified Mie theory. On the other hand, when Mie theory is consistently applied in both OA absorptivity retrieval and the RTM, the errors largely cancel out, yielding accurate DRE. As long as global RTMs use Mie theory, they should implement parametrizations of light-absorbing OA derived from retrievals based on Mie theory.

  19. Parameterization of clear-sky surface irradiance and its implications for estimation of aerosol direct radiative effect and aerosol optical depth

    PubMed Central

    Xia, Xiangao

    2015-01-01

    Aerosols impact clear-sky surface irradiance () through the effects of scattering and absorption. Linear or nonlinear relationships between aerosol optical depth (τa) and have been established to describe the aerosol direct radiative effect on (ADRE). However, considerable uncertainties remain associated with ADRE due to the incorrect estimation of (τa in the absence of aerosols). Based on data from the Aerosol Robotic Network, the effects of τa, water vapor content (w) and the cosine of the solar zenith angle (μ) on are thoroughly considered, leading to an effective parameterization of as a nonlinear function of these three quantities. The parameterization is proven able to estimate with a mean bias error of 0.32 W m−2, which is one order of magnitude smaller than that derived using earlier linear or nonlinear functions. Applications of this new parameterization to estimate τa from , or vice versa, show that the root-mean-square errors were 0.08 and 10.0 Wm−2, respectively. Therefore, this study establishes a straightforward method to derive from τa or estimate τa from measurements if water vapor measurements are available. PMID:26395310

  20. Simultaneous retrieval of aerosol properties and clear-sky direct radiative effect over the global ocean from MODIS

    NASA Astrophysics Data System (ADS)

    Lee, Jaehwa; Kim, Jhoon; Lee, Yun Gon

    2014-08-01

    A unified satellite algorithm is presented to simultaneously retrieve aerosol properties (aerosol optical depth; AOD and aerosol type) and clear-sky shortwave direct radiative effect (hereafter, DREA) over ocean. The algorithm is applied to Moderate Resolution Imaging spectroradiometer (MODIS) observations for a period from 2003 to 2010 to assess the DREA over the global ocean. The simultaneous retrieval utilizes lookup table (LUT) containing both spectral reflectances and solar irradiances calculated using a single radiative transfer model with the same aerosol input data. This study finds that aerosols cool the top-of-atmosphere (TOA) and bottom-of-atmosphere (BOA) by 5.2 ± 0.5 W/m2 and 8.3 W/m2, respectively, and correspondingly warm the atmosphere (hereafter, ATM) by 3.1 W/m2. These quantities, solely based on the MODIS observations, are consistent with those of previous studies incorporating chemical transport model simulations and satellite observations. However, the DREAs at BOA and ATM are expected to be less accurate compared to that of TOA due to low sensitivity in retrieving aerosol type information, which is related with the atmospheric heating by aerosols, particularly in low AOD conditions; consequently, the uncertainties could not be quantified. Despite the issue in the aerosol type information, the present method allows us to confine the DREA attributed only to fine-mode dominant aerosols, which are expected to be mostly anthropogenic origin, in the range from -1.1 W/m2 to -1.3 W/m2 at TOA. Improvements in size-resolved AOD and SSA retrievals from current and upcoming satellite instruments are suggested to better assess the DREA, particularly at BOA and ATM, where aerosol absorptivity induces substantial uncertainty.

  1. Direct aerosol effects during periods of solar dimming and brightening hidden in the regression residuals: Evidence from Potsdam measurements

    NASA Astrophysics Data System (ADS)

    Vetter, Tobias; Wechsung, Frank

    2015-11-01

    A recent empirical study of Stanhill et al. (2014), which was based on the Angstrom-Prescott relationship between global radiation and sunshine duration, was evaluated. The parameters of this relationship seemed to be rather stable across the dimming and brightening periods. Thus, the authors concluded that the variation in global radiation is more influenced by changes in cloud cover and sunshine duration than by the direct aerosol effects. In our study, done for the Potsdam station (one of six globally distributed stations, the source of one of the longest observational records and closely located to former hot spots of aerosol emission), we tested and rejected the hypothesis that the dimming of global radiation directly caused by aerosols is negligible. The residuals of the Angstrom-Prescott regression reveal a statistically significant positive temporal trend and a temporal level segmentation. The latter was consistent with the temporal emission patterns around Potsdam. The trend in the residuals only disappeared when the model intercept varied according to the temporal level segmentation. The magnitude of the direct aerosol effect on the level changes in global radiation derived from the modified Angstrom-Prescott relationship was in the range indicated in previous studies. Thus, from here, a specific request cannot be made for a revision of current climate models state-of-the-art representation of both the cooling effect directly caused by aerosols and the temperature sensitivity to the increase of greenhouse gases.

  2. Diurnal variations of aerosol optical properties in the North China Plain and their influences on the estimates of direct aerosol radiative effect

    NASA Astrophysics Data System (ADS)

    Kuang, Ye; Zhao, Chunsheng

    2016-04-01

    In this paper, the diurnal variations of aerosol optical properties and their influences on the estimation of daily average direct aerosol radiative effect (DARE) in the North China Plain (NCP) are investigated based on in situ measurements from Haze in China campaign. For ambient aerosol, the diurnal patterns of single scattering albedo (SSA) and asymmetry factor (g) in the NCP are both highest at dawn and lowest in the late afternoon, and quite different from those of dry-state aerosol. The relative humidity is the dominant factor which determines the diurnal patterns of SSA and g for ambient aerosol. Basing on the calculated SSA and g, several cases are designed to investigate the impacts of the diurnal changes of aerosol optical properties on DARE. The results demonstrate that the diurnal changes of SSA and g in the NCP have significant influences on the estimation of DARE at the top of the atmosphere (TOA). If the full temporal coverage of aerosol optical depth (AOD), SSA and g are available, an accurate estimation of daily average DARE can be achieved by using the daily averages of AOD, SSA and g. However, due to the lack of full temporal coverage datasets of SSA and g, their daily averages are usually not available. Basing on the results of designed cases, if the RH plays a dominant role in the diurnal variations of SSA and g, we suggest that using both SSA and g averaged over early morning and late afternoon as inputs for radiative transfer model to improve the accurate estimation of DARE. If the temporal samplings of SSA or g are too few to adopt this method, either averaged over early morning or late afternoon of both SSA and g can be used to improve the estimation of DARF at TOA.

  3. Top-of-Atmosphere Direct Radiative Effect of Aerosols over Global Oceans from Merged CERES and MODIS Observations

    NASA Technical Reports Server (NTRS)

    Loeb, N. G.; Smith, N. M.

    2004-01-01

    The direct radiative effect of aerosols (DREA) is defined as the difference between radiative fluxes in the absence and presence of aerosols. In this study, the direct radiative effect of aerosols is estimated for 46 months (March, 2000 to December, 2003) of merged CERES and MODIS Terra global measurements over ocean. This analysis includes the contribution from clear regions in both clear and partly cloudy CERES footprints. MODIS-CERES narrow-to-broadband regressions are developed to convert clear-sky MODIS narrowband radiances to broadband SW radiances, and CERES clear-sky Angular Distribution Models (ADMs) are used to estimate the corresponding TOA radiative fluxes needed to determine the DREA. Clear-sky MODIS pixels are identified using two independent cloud masks: (i) the NOAA-NESDIS algorithm used for inferring aerosol properties from MODIS on the CERES Single Scanner Footprint TOA/Surface Fluxes and Clouds (SSF) product (NOAA-SSF); and (ii) the standard algorithm used by the MODIS aerosol group to produce the MODO4 product (MODO4). Over global oceans, direct radiative cooling by aerosols for clear scenes identified from MODO4 is estimated to be 5.5 W m-2, compared to 3.8 W m-2 for clear scenes from NOAA-SSF. Regionally, differences are largest in areas affected by dust aerosol, such as oceanic regions adjacent to the Saharan and Saudi Arabian deserts, and in northern Pacific Ocean regions influenced by dust transported from Asia. The net total-sky (clear and cloudy) DREA is negative (cooling) and is estimated to be -2.0 W m-2 from MOD04, and -1.6 W m-2 from NOAA-SSF. The DREA is shown to have pronounced seasonal cycles in the Northern Hemisphere and large year-to-year fluctuations near deserts. However, no systematic trend in deseasonalized anomalies of the DREA is observed over the 46-month time series considered.

  4. A Novel Method for Estimating Shortwave Direct Radiative Effect of Above-Cloud Aerosols Using CALIOP and MODIS Data

    NASA Technical Reports Server (NTRS)

    Zhang, Z.; Meyer, K.; Platnick, S.; Oreopoulos, L.; Lee, D.; Yu, H.

    2014-01-01

    This paper describes an efficient and unique method for computing the shortwave direct radiative effect (DRE) of aerosol residing above low-level liquid-phase clouds using CALIOP and MODIS data. It accounts for the overlapping of aerosol and cloud rigorously by utilizing the joint histogram of cloud optical depth and cloud top pressure. Effects of sub-grid scale cloud and aerosol variations on DRE are accounted for. It is computationally efficient through using grid-level cloud and aerosol statistics, instead of pixel-level products, and a pre-computed look-up table in radiative transfer calculations. We verified that for smoke over the southeast Atlantic Ocean the method yields a seasonal mean instantaneous shortwave DRE that generally agrees with more rigorous pixel-level computation within 4. We have also computed the annual mean instantaneous shortwave DRE of light-absorbing aerosols (i.e., smoke and polluted dust) over global ocean based on 4 yr of CALIOP and MODIS data. We found that the variability of the annual mean shortwave DRE of above-cloud light-absorbing aerosol is mainly driven by the optical depth of the underlying clouds.

  5. 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...

  6. Investigation on the direct radiative effect of fossil fuel black-carbon aerosol over China

    NASA Astrophysics Data System (ADS)

    Zhuang, Bingliang; Jiang, Fei; Wang, Tijian; Li, Shu; Zhu, Bin

    2011-06-01

    In China, due to lack of countrywide monitoring and coarse emission inventory of black carbon (BC) in early years, there are large uncertainties as to the estimations of its loading, direct radiative forcing (DRF) and climate response. Here, we apply an up-to-date emission inventory of BC in 2006 to investigate its loading, optical depth (AOD) at 550 nm and DRF using the coupled Regional Climate Chemistry Modeling System (RegCCMS). A state of the art air quality model (WRF/Chem) is also used to access surface BC concentration. Simulated surface concentrations of BC from these two models were compared with observations, while the AOD was compared with the results both from the Goddard Chemistry Aerosol Radiation and Transport (GOCART) model and from satellite and ground-based simulations. Results show that RegCCMS presented similar patterns and levels of annual mean-surface BC concentration to those of WRF/Chem. The regional distributions and monthly variations of RegCCMS BC were reproduced well in comparison to observations. Simulated pattern of AODs are consistent to but lower than those from satellite (Omi-0.25°) and AERONET simulations. Annual mean DRFs mainly distribute in the area with high BC loadings, with regional mean of 0.75 W m-2 and predicted global mean of 0.343 W m-2. In general, the results are about 0.4-5 times for regional column burden, about 2 times as high for regional mean DRFs, about 1.3-1.8 times for global mean DRFs and about 3-4 times for AOD at 550 nm as compared to those in previous studies in China. These increasing DRFs of BC imply that its warming effect and climate response should be stronger and the DRF of total aerosols should be weaker (less negative).

  7. Assesment of the Indirect and Semi-Direct Aerosol-Effect During ISDAC Through Integrated Observational and Modeling Studies

    SciTech Connect

    Boybeyi, Zafer

    2014-09-29

    The Department of Energy (DOE) awarded George Mason University (GMU) with a research project. This project started on June, 2009 and ended July 2014. Main objectives of this research project are; a) to assess the indirect and semi-direct aerosol effects on microphysical structure and radiative properties of Arctic clouds, b) to assess the impact of feedback between the aerosol-cloud interactions and atmospheric boundary layer (ABL) processes on the surface energy balance, c) to better understand and characterize the important unresolved microphysical processes, aerosol effects, and ABL processes and feedbacks, over meso-γ spatial (~1-2 km) and temporal scales (a few minutes to days), and d) to investigate the scale dependency of microphysical parameterizations and its effect on simulations.

  8. Global modelling of direct and indirect effects of sea spray aerosol using a source function encapsulating wave state

    NASA Astrophysics Data System (ADS)

    Partanen, A.-I.; Dunne, E. M.; Bergman, T.; Laakso, A.; Kokkola, H.; Ovadnevaite, J.; Sogacheva, L.; Baisnée, D.; Sciare, J.; Manders, A.; O'Dowd, C.; de Leeuw, G.; Korhonen, H.

    2014-11-01

    Recently developed parameterizations for the sea spray aerosol source flux, encapsulating wave state, and its organic fraction were incorporated into the aerosol-climate model ECHAM-HAMMOZ to investigate the direct and indirect radiative effects of sea spray aerosol particles. Our simulated global sea salt emission of 805 Tg yr-1 (uncertainty range 378-1233 Tg yr-1) was much lower than typically found in previous studies. Modelled sea salt and sodium ion concentrations agreed relatively well with measurements in the smaller size ranges at Mace Head (annual normalized mean model bias -13% for particles with vacuum aerodynamic diameter Dva < 1 μm), Point Reyes (-29% for particles with aerodynamic diameter Da < 2.5 μm) and Amsterdam Island (-52% for particles with Da < 1 μm) but the larger sizes were overestimated (899% for particles with 2.5 μm < Da < 10 μm) at Amsterdam Island. This suggests that at least the high end of the previous estimates of sea spray mass emissions is unrealistic. On the other hand, the model clearly underestimated the observed concentrations of organic or total carbonaceous aerosol at Mace Head (-82%) and Amsterdam Island (-68%). The large overestimation (212%) of organic matter at Point Reyes was due to the contribution of continental sources. At the remote Amsterdam Island site, the organic concentration was underestimated especially in the biologically active months, suggesting a need to improve the parameterization of the organic sea spray fraction. Globally, the satellite-retrieved AOD over the oceans, using PARASOL data, was underestimated by the model (means over ocean 0.16 and 0.10, respectively); however, in the pristine region around Amsterdam Island the measured AOD fell well within the simulated uncertainty range. The simulated sea spray aerosol contribution to the indirect radiative effect was positive (0.3 W m-2), in contrast to previous studies. This positive effect was ascribed to the tendency of sea salt aerosol to

  9. Impacts of the direct radiative effect of aerosols in numerical weather prediction over Europe using the ALADIN-HIRLAM NWP system

    NASA Astrophysics Data System (ADS)

    Toll, V.; Gleeson, E.; Nielsen, K. P.; Männik, A.; Mašek, J.; Rontu, L.; Post, P.

    2016-05-01

    Aerosol feedbacks are becoming more accepted as physical mechanisms that should be included in numerical weather prediction models in order to improve the accuracy of the weather forecasts. The default set-up in the Aire Limitee Adaptation dynamique Developpement INternational (ALADIN) - High Resolution Limited Area Model (HIRLAM) numerical weather prediction system includes monthly aerosol climatologies to account for the average direct radiative effect of aerosols. This effect was studied using the default aerosol climatology in the system and compared to experiments run using the more up-to-date Max-Planck-Institute Aerosol Climatology version 1 (MACv1), and time-varying aerosol data from the Monitoring Atmospheric Composition and Climate (MACC) reanalysis aerosol dataset. Accounting for the direct radiative effect using monthly aerosol climatologies or near real-time aerosol distributions improved the accuracy of the simulated radiative fluxes and temperature and humidity forecasts in the lower troposphere. However, the dependency of forecast meteorological conditions on the aerosol dataset itself was found to be weak.

  10. A Novel Method for Estimating Shortwave Direct Radiative Effect of Above-Cloud Aerosols Using CALIOP and MODIS Data

    NASA Technical Reports Server (NTRS)

    Zhang, Zhibo; Meyer, Kerry G.; Platnick, Steven; Oreopoulos, Lazaros; Lee, Dongmin; Yu, Hongbin

    2014-01-01

    This paper describes an efficient and unique method for computing the shortwave direct radiative effect (DRE) of aerosol residing above low-level liquid-phase clouds using CALIOP and MODIS data. It addresses the overlap of aerosol and cloud rigorously by utilizing the joint histogram of cloud optical depth and cloud top pressure while also accounting for subgrid-scale variations of aerosols. The method is computationally efficient because of its use of grid-level cloud and aerosol statistics, instead of pixel-level products, and a pre-computed look-up table based on radiative transfer calculations. We verify that for smoke over the southeast Atlantic Ocean the method yields a seasonal mean instantaneous (approximately 1:30PM local time) shortwave DRE of above cloud aerosol (ACA) that generally agrees with more rigorous pixel-level computation within 4 percent. We also estimate the impact of potential CALIOP aerosol optical depth (AOD) retrieval bias of ACA on DRE. We find that the regional and seasonal mean instantaneous DRE of ACA over southeast Atlantic Ocean would increase, from the original value of 6.4 W m(-2) based on operational CALIOP AOD to 9.6 W m(-2) if CALIOP AOD retrieval are biased low by a factor of 1.5 (Meyer et al., 2013) and further to 30.9 W m(-2) if CALIOP AOD retrieval are biased low by a factor of 5 as suggested in (Jethva et al., 2014). In contrast, the instantaneous ACA radiative forcing efficiency (RFE) remains relatively invariant in all cases at about 53 W m(-2) AOD(-1), suggesting a near linear relation between the instantaneous RFE and AOD. We also compute the annual mean instantaneous shortwave DRE of light-absorbing aerosols (i.e., smoke and polluted dust) over global oceans based on 4 years of CALIOP and MODIS data. We find that the variability of the annual mean shortwave DRE of above-cloud light-absorbing aerosol is mainly driven by the optical depth of the underlying clouds. While we demonstrate our method using CALIOP and MODIS

  11. On the use of satellite remote sensing to determine aerosol direct radiative effect over land: A case study over China

    NASA Astrophysics Data System (ADS)

    Sundström, Anu-Maija; Arola, Antti; Kolmonen, Pekka; de Leeuw, Gerrit

    2014-05-01

    The quantification of aerosol radiative effects is complex and large uncertainties still exist, mainly due to the high spatial and temporal variation of the aerosol concentration and mass as well as their relatively short lifetime in the atmosphere. In this work a multi-sensor satellite based approach is studied for defining the direct short wave aerosol radiative effect (ADRE) over China. ADRE at the top of the atmosphere (TOA) is defined as the difference between the net solar flux with (F ) and without (F0) aerosols. The negative values of ADRE correspond to increased outgoing radiation and planetary cooling, whereas positive values correspond to decreased outgoing radiation at TOA and increased atmospheric warming. To derive instantaneous ADRE from the satellite observations, the challenge is to estimate the value for F0. In this work F0 is derived using the colocated observations of CERES (Clouds and the Earth's Radian Energy System) short wave broad band TOA-flux for cloud free sky and MODIS (Moderate Imaging Spectroradiometer) aerosol optical depth (AOD). Assuming that aerosol type does not change systematically within a 0.5 deg. grid cell over a month, a linear relationship is established between the clear-sky TOA-fluxes and AODs. Using the linear regression an estimate for instantaneous monthly F0 can be obtained by extrapolating the line to AOD=0, while F is the monthly mean of cloud free CERES observations. However, there are several other parameters affecting the observed TOA flux than the aerosol loading and aerosol type, such as solar zenith angle, water vapour, land surface albedo and Earth-Sun distance. Changes in these parameters within a grid cell over a month inflect the correlation between AOD and TOA fluxes. To minimize the effect of zenith angle, water vapour, and Earth-Sun distance the CERES fluxes are normalized before the linear fitting using reference fluxes calculated with a radiative transfer code (Libradtran). The normalization

  12. Aerosol direct radiative effects over the northwest Atlantic, northwest Pacific, and North Indian Oceans: estimates based on in-situ chemical and optical measurements and chemical transport modeling

    NASA Astrophysics Data System (ADS)

    Bates, T. S.; Anderson, T. L.; Baynard, T.; Bond, T.; Boucher, O.; Carmichael, G.; Clarke, A.; Erlick, C.; Guo, H.; Horowitz, L.; Howell, S.; Kulkarni, S.; Maring, H.; McComiskey, A.; Middlebrook, A.; Noone, K.; O'Dowd, C. D.; Ogren, J.; Penner, J.; Quinn, P. K.; Ravishankara, A. R.; Savoie, D. L.; Schwartz, S. E.; Shinozuka, Y.; Tang, Y.; Weber, R. J.; Wu, Y.

    2006-05-01

    The largest uncertainty in the radiative forcing of climate change over the industrial era is that due to aerosols, a substantial fraction of which is the uncertainty associated with scattering and absorption of shortwave (solar) radiation by anthropogenic aerosols in cloud-free conditions (IPCC, 2001). Quantifying and reducing the uncertainty in aerosol influences on climate is critical to understanding climate change over the industrial period and to improving predictions of future climate change for assumed emission scenarios. Measurements of aerosol properties during major field campaigns in several regions of the globe during the past decade are contributing to an enhanced understanding of atmospheric aerosols and their effects on light scattering and climate. The present study, which focuses on three regions downwind of major urban/population centers (North Indian Ocean (NIO) during INDOEX, the Northwest Pacific Ocean (NWP) during ACE-Asia, and the Northwest Atlantic Ocean (NWA) during ICARTT), incorporates understanding gained from field observations of aerosol distributions and properties into calculations of perturbations in radiative fluxes due to these aerosols. This study evaluates the current state of observations and of two chemical transport models (STEM and MOZART). Measurements of burdens, extinction optical depth (AOD), and direct radiative effect of aerosols (DRE - change in radiative flux due to total aerosols) are used as measurement-model check points to assess uncertainties. In-situ measured and remotely sensed aerosol properties for each region (mixing state, mass scattering efficiency, single scattering albedo, and angular scattering properties and their dependences on relative humidity) are used as input parameters to two radiative transfer models (GFDL and University of Michigan) to constrain estimates of aerosol radiative effects, with uncertainties in each step propagated through the analysis. Constraining the radiative transfer

  13. Aerosol Direct Radiative Effects Over the Northwest Atlantic, Northwest Pacific, and North Indian Oceans: Estimates Based on In-situ Chemical and Optical Measurements and Chemical Transport Modeling

    NASA Astrophysics Data System (ADS)

    Bates, T. S.; Anderson, T. L.; Baynard, T.; Bond, T.; Boucher, O.; Carmichael, G.; Clarke, A.; Erlick, C.; Guo, H.; Horowitz, L.; Howell, S.; Kulkarni, S.; Maring, H.; McComiskey, A.; Middlebrook, A.; Noone, K.; O'Dowd, C. D.; Ogren, J. A.; Penner, J.; Quinn, P. K.; Ravishankara, A. R.; Savoie, D. L.; Schwartz, S. E.; Shinozuka, Y.; Tang, Y.; Weber, R. J.; Wu, Y.

    2005-12-01

    The largest uncertainty in the radiative forcing of climate change over the industrial era is that due to aerosols, a substantial fraction of which is the uncertainty associated with scattering and absorption of shortwave (solar) radiation by anthropogenic aerosols in cloud-free conditions. Quantifying and reducing the uncertainty in aerosol influences on climate is critical to understanding climate change over the industrial period and to improving predictions of future climate change for assumed emission scenarios. Measurements of aerosol properties during major field campaigns in several regions of the globe during the past decade are contributing to an enhanced understanding of atmospheric aerosols and their effects on light scattering and climate. The present study, which focuses on three regions downwind of major urban/population centers (North Indian Ocean during INDOEX, the Northwest Pacific Ocean during ACE-Asia, and the Northwest Atlantic Ocean during ICARTT), incorporates understanding gained from field observations of aerosol distributions and properties into calculations of perturbations in radiative fluxes due to these aerosols. This study evaluates the current state of observations and of two chemical transport models (STEM and MOZART). Measurements of burdens, extinction optical depth, and direct radiative effect of aerosols (change in radiative flux due to total aerosols) are used as measurement-model check points to assess uncertainties. In-situ measured and remotely sensed aerosol properties for each region (mixing state, mass scattering efficiency, single scattering albedo, and angular scattering properties and their dependences on relative humidity) are used as input parameters to two radiative transfer models (GFDL and University of Michigan) to constrain estimates of aerosol radiative effects, with uncertainties in each step propagated through the analysis. Such comparisons with observations and resultant reductions in uncertainties are

  14. Satellite-Based Assessment of Possible Dust Aerosols Semi-Direct Effect on Cloud Water Path over East Asia

    NASA Technical Reports Server (NTRS)

    Huang, Jianping; Lin, Bing; Minnis, Patrick; Wang, Tainhe; Wang, Xin; Hu, Yongxiang; Yi, Yuhong; Ayers, J. Kirk

    2006-01-01

    The semi-direct effects of dust aerosols are analyzed over eastern Asia using 2 years (June 2002 to June 2004) of data from the Clouds and the Earth s Radiant Energy System (CERES) scanning radiometer and MODerate Resolution Imaging Spectroradiometer (MODIS) on the Aqua satellite, and 18 years (1984 to 2001) of International Satellite Cloud Climatology Project (ISCCP) data. The results show that the water path of dust-contaminated clouds is considerably smaller than that of dust-free clouds. The mean ice water path (IWP) and liquid water path (LWP) of dusty clouds are less than their dust-free counterparts by 23.7% and 49.8%, respectively. The long-term statistical relationship derived from ISCCP also confirms that there is significant negative correlation between dust storm index and ISCCP cloud water path. These results suggest that dust aerosols warm clouds, increase the evaporation of cloud droplets and further reduce cloud water path, the so-called semi-direct effect. The semi-direct effect may play a role in cloud development over arid and semi-arid areas of East Asia and contribute to the reduction of precipitation.

  15. Shortwave direct radiative effects of above cloud aerosols over global oceans derived from eight years of CALIOP and MODIS observations

    NASA Astrophysics Data System (ADS)

    Zhang, Z.; Meyer, K.; Yu, H.; Platnick, S.; Colarco, P.; Liu, Z.; Oreopoulos, L.

    2015-09-01

    In this paper, we studied the frequency of occurrence and shortwave direct radiative effects (DRE) of above-cloud aerosols (ACAs) over global oceans using eight years of collocated CALIOP and MODIS observations. Similar to previous work, we found high ACA occurrence in four regions: Southeast (SE) Atlantic region where ACAs are mostly light-absorbing aerosols, i.e., smoke and polluted dust according to CALIOP classification, originating from biomass burning over African Savanna; Tropical Northeast Atlantic and Arabian Sea where ACAs are predominantly windblown dust from the Sahara and Arabian desert, respectively; and Northwest Pacific where ACAs are mostly transported smoke and polluted dusts from Asian. From radiative transfer simulations based on CALIOP-MODIS observations and a set of the preselected aerosol optical models, we found the DREs of ACAs at the top of atmosphere (TOA) to be positive (i.e., warming) in the SE Atlantic and NW Pacific regions, but negative (i.e., cooling) in TNE Atlantic and Arabian Sea. The cancellation of positive and negative regional DREs results in a global ocean annual mean diurnally averaged cloudy-sky DRE of 0.015 W m-2 (range of -0.03 to 0.06 W m-2) at TOA. The DREs at surface and within atmosphere are -0.15 W m-2 (range of -0.09 to -0.21 W m-2), and 0.17 W m-2 (range of 0.11 to 0.24 W m-2), respectively. The regional and seasonal mean DREs are much stronger. For example, in the SE Atlantic region the JJA (July ~ August) seasonal mean cloudy-sky DRE is about 0.7 W m-2 (range of 0.2 to 1.2 W m-2) at TOA. The uncertainty in our DRE computations is mainly cause by the uncertainties in the aerosol optical properties, in particular aerosol absorption, and uncertainties in the CALIOP operational aerosol optical thickness retrieval. In situ and remotely sensed measurements of ACA from future field campaigns and satellite missions, and improved lidar retrieval algorithm, in particular vertical feature masking, would help reduce the

  16. Aerosol direct radiative effects over the northwest Atlantic, northwest Pacific, and North Indian Oceans: estimates based on in-situ chemical and optical measurements and chemical transport modeling

    NASA Astrophysics Data System (ADS)

    Bates, T. S.; Anderson, T. L.; Baynard, T.; Bond, T.; Boucher, O.; Carmichael, G.; Clarke, A.; Erlick, C.; Guo, H.; Horowitz, L.; Howell, S.; Kulkarni, S.; Maring, H.; McComiskey, A.; Middlebrook, A.; Noone, K.; O'Dowd, C. D.; Ogren, J.; Penner, J.; Quinn, P. K.; Ravishankara, A. R.; Savoie, D. L.; Schwartz, S. E.; Shinozuka, Y.; Tang, Y.; Weber, R. J.; Wu, Y.

    2006-01-01

    The largest uncertainty in the radiative forcing of climate change over the industrial era is that due to aerosols, a substantial fraction of which is the uncertainty associated with scattering and absorption of shortwave (solar) radiation by anthropogenic aerosols in cloud-free conditions (IPCC, 2001). Quantifying and reducing the uncertainty in aerosol influences on climate is critical to understanding climate change over the industrial period and to improving predictions of future climate change for assumed emission scenarios. Measurements of aerosol properties during major field campaigns in several regions of the globe during the past decade are contributing to an enhanced understanding of atmospheric aerosols and their effects on light scattering and climate. The present study, which focuses on three regions downwind of major urban/population centers (North Indian Ocean (NIO) during INDOEX, the Northwest Pacific Ocean (NWP) during ACE-Asia, and the Northwest Atlantic Ocean (NWA) during ICARTT), incorporates understanding gained from field observations of aerosol distributions and properties into calculations of perturbations in radiative fluxes due to these aerosols. This study evaluates the current state of observations and of two chemical transport models (STEM and MOZART). Measurements of burdens, extinction optical depth (AOD), and direct radiative effect of aerosols (DRE - change in radiative flux due to total aerosols) are used as measurement-model check points to assess uncertainties. In-situ measured and remotely sensed aerosol properties for each region (mixing state, mass scattering efficiency, single scattering albedo, and angular scattering properties and their dependences on relative humidity) are used as input parameters to two radiative transfer models (GFDL and University of Michigan) to constrain estimates of aerosol radiative effects, with uncertainties in each step propagated through the analysis. Constraining the radiative transfer

  17. The Fully Online Integrated Model System COSMO-ART to Simulate Direct and Indirect Effects of Aerosols

    NASA Astrophysics Data System (ADS)

    Vogel, B.; Athanasopoulou, E.; Bangert, M.; Ferrone, A.; Lundgren, K.; Vogel, H.; Knote, Ch.; Brunner, D.

    2012-04-01

    The interplay between air quality and regional climate has become a focal point in recent atmospheric research. The treatment of the interaction of the involved processes requires a new class of air quality models. The fully online integrated model system COSMO-ART was developed (Vogel et al., 2009, Bangert et al., 2010) to quantify the feedback processes between aerosols and the state of the atmosphere on the continental to the regional scale with two-way interactions between different atmospheric processes. The meteorological driver is the operational weather forecast model of the Deutscher Wetterdienst (German Weather Service, DWD). The model system treats secondary aerosols as well as directly emitted components like soot, mineral dust, sea salt, volcanic ash and biological material. Secondary aerosol particles are formed from the gas phase. Therefore, a complete gas phase mechanism (RADMKA) is included in COSMO-ART. Modules for the emissions of biogenic precursors of aerosols, mineral dust, sea salt, biomass burning aerosol and pollen grains are included. For the treatment of secondary organic aerosol (SOA) chemistry the volatility basis set (VBS) was included. Wet scavenging and in-cloud chemistry are taken into account (Knote, 2012). To simulate the impact of the various aerosol particles on the cloud microphysics and precipitation COSMO-ART was coupled with the two-moment cloud microphysics scheme of Seifert and Beheng (2006) by using comprehensive parameterisations for aerosol activation and ice nucleation. The model system was applied for a different model domains and meteorological situations to quantify the direct and the indirect of the various aerosol particles. Studies over a few days as well as over longer time periods were carried out. Results of the simulations of the heat wave of 2003 taken into account all included particles will be shown as well as results of simulations of May 2008 focusing on the contribution of specific aerosol particles, e

  18. Interpreting the ultraviolet aerosol index observed with the OMI satellite instrument to understand absorption by organic aerosols: implications for atmospheric oxidation and direct radiative effects

    NASA Astrophysics Data System (ADS)

    Hammer, Melanie S.; Martin, Randall V.; van Donkelaar, Aaron; Buchard, Virginie; Torres, Omar; Ridley, David A.; Spurr, Robert J. D.

    2016-03-01

    , thus reducing the bias against observed values. We calculate the direct radiative effect (DRE) of BrC using GEOS-Chem coupled with the radiative transfer model RRTMG (GC-RT). Treating organic aerosol as containing more strongly absorbing BrC changes the global annual mean all-sky top of atmosphere (TOA) DRE by +0.03 W m-2 and all-sky surface DRE by -0.08 W m-2. Regional changes of up to +0.3 W m-2 at TOA and down to -1.5 W m-2 at the surface are found over major biomass burning regions.

  19. Interpreting the Ultraviolet Aerosol Index observed with the OMI satellite instrument to understand absorption by organic aerosols: implications for atmospheric oxidation and direct radiative effects

    NASA Astrophysics Data System (ADS)

    Hammer, M. S.; Martin, R. V.; van Donkelaar, A.; Buchard, V.; Torres, O.; Ridley, D. A.; Spurr, R. J. D.

    2015-10-01

    reducing the bias against observed values. We calculate the direct radiative effect (DRE) of BrC using GEOS-Chem coupled with the radiative transfer model RRTMG (GC-RT). Treating organic aerosol as containing absorbing BrC rather than as primarily scattering changes global annual mean all-sky top of atmosphere (TOA) DRE by +0.05 W m-2 and all-sky surface DRE by -0.06 W m-2. Regional changes of up to +0.5 W m-2 at TOA and down to -1 W m-2 at the surface are found over major biomass burning regions.

  20. Interpreting the Ultraviolet Aerosol Index Observed with the OMI Satellite Instrument to Understand Absorption by Organic Aerosols: Implications for Atmospheric Oxidation and Direct Radiative Effects

    NASA Technical Reports Server (NTRS)

    Hammer, Melanie S.; Martin, Randall V.; Donkelaar, Aaron van; Buchard, Virginie; Torres, Omar; Ridley, David A.; Spurr, Robert J. D.

    2016-01-01

    reducing the bias against observed values. We calculate the direct radiative effect (DRE) of BrC using GEOS-Chem coupled with the radiative transfer model RRTMG (GC-RT). Treating organic aerosol as containing more strongly absorbing BrC changes the global annual mean all-sky top of atmosphere (TOA) DRE by +0.03Wm(exp -2) and all-sky surface DRE by -0.08Wm(exp -2). Regional changes of up to +0.3Wm(exp -2) at TOA and down to -1.5Wm(exp -2) at the surface are found over major biomass burning regions.

  1. Top-of-Atmosphere Direct Radiative Effect of Aerosols from the Clouds and the Earth's Radiant Energy System Satellite Instrument (CERES)

    NASA Technical Reports Server (NTRS)

    Loeb, N. G.; Kato, S.

    2002-01-01

    Nine months of CERES/TRMM broadband fluxes combined with VIRS high-resolution imager measurements are used to estimate the daily average direct radiative effect of aerosols for clear-sky conditions over the tropical oceans. On average, aerosols have a cooling effect over the tropics of 4.6 +/- 1 W/sq m. The magnitude is approx.2 W/sq m smaller over the southern tropical oceans than it is over northern tropical oceans. The direct effect derived from CERES is highly correlated with coincident aerosol optical depth retrievals inferred from 0.63 microns VIRS radiances (correlation coefficient of 0.96). The slope of the regression line is approx. -32 W/sq m/t over the equatorial Pacific Ocean, but changes both regionally and seasonally, depending on the aerosol characteristics. Near sources of biomass burning and desert dust, the aerosol direct effect reaches -25 W sq m to -30 W/sq m. The direct effect from CERES also shows a dependence on wind speed. The reason for this dependence is unclear-it may be due to increased aerosol (e.g. sea-salt or aerosol transport) or increased surface reflection (e.g. due to whitecaps). The uncertainty in the tropical average direct effect from CERES is approx. 1 W/sq m (approx. 20%) due mainly to cloud contamination, the radiance-to-flux conversion, and instrument calibration. By comparison, uncertainties in the direct effect from the ERBE and CERES "ERBE-Like" products are a factor of 3 to 5 larger.

  2. First results on the direct effects of aerosols in the Brazilian Earth System Model

    NASA Astrophysics Data System (ADS)

    Pendharkar, J.; Alvim, D. S., Sr.; Figueroa, S. N.; Nobre, P. N.; Kubota, P. Y.

    2015-12-01

    Brazilian Earth System Model (BESM) is being developed at Instituto Nacional de Pesquisas Espaciais (INPE), Brazil with a mission to build and utilize the potential to generate scenarios for future climate change, represent in the best capacity the processes relevant to Brazil's interest thereby playing a lead role in determining policies pertaining to environment and climate change, and participate in the IPCC global climate change scenarios. One of the developmental goals of BESM is to simulate the affects of aerosols in its climate model. The Hamburg Aerosol Model (HAM) is been chosen as the aerosol transport module for BESM. The implementation is categorized in three phases, of which the initialization phase has been completed. The work is underway to include the radiative affect of aerosols. We propose to present the first results of the implementation of the radiative affects of the aerosols that is, radiative forcing over different regions of Brazil with sector specific environmental conditions like forest fires, industrial, domestic etc. The initial simulations will be crucial for the BESM and will also shed light on the performance of the different radiation schemes in BESM and to its response to aerosols.

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

    EPA Science Inventory

    A comprehensive investigation of the processes regulating tropospheric aerosol distributions, their optical properties, and their radiative effects in conjunction with verification of their simulated radiative effects for past conditions relative to measurements is needed in orde...

  4. Effect of Spectrally Varying Albedo of Vegetation Surfaces on Shortwave Radiation Fluxes and Aerosol Direct Radiative Forcing

    NASA Technical Reports Server (NTRS)

    Zhu, L.; Martins, J. V.; Yu, H.

    2012-01-01

    This study develops an algorithm for representing detailed spectral features of vegetation albedo based on Moderate Resolution Imaging Spectrometer (MODIS) observations at 7 discrete channels, referred to as the MODIS Enhanced Vegetation Albedo (MEVA) algorithm. The MEVA algorithm empirically fills spectral gaps around the vegetation red edge near 0.7 micrometers and vegetation water absorption features at 1.48 and 1.92 micrometers which cannot be adequately captured by the MODIS 7 channels. We then assess the effects of applying MEVA in comparison to four other traditional approaches to calculate solar fluxes and aerosol direct radiative forcing (DRF) at the top of atmosphere (TOA) based on the MODIS discrete reflectance bands. By comparing the DRF results obtained through the MEVA method with the results obtained through the other four traditional approaches, we show that filling the spectral gap of the MODIS measurements around 0.7 micrometers based on the general spectral behavior of healthy green vegetation leads to significant improvement in the instantaneous aerosol DRF at TOA (up to 3.02Wm(exp -2) difference or 48% fraction of the aerosol DRF, .6.28Wm(exp -2), calculated for high spectral resolution surface reflectance from 0.3 to 2.5 micrometers for deciduous vegetation surface). The corrections of the spectral gaps in the vegetation spectrum in the near infrared, again missed by the MODIS reflectances, also contributes to improving TOA DRF calculations but to a much lower extent (less than 0.27Wm(exp -2), or about 4% of the instantaneous DRF). Compared to traditional approaches, MEVA also improves the accuracy of the outgoing solar flux between 0.3 to 2.5 micrometers at TOA by over 60Wm(exp -2) (for aspen 3 surface) and aerosol DRF by over 10Wm(exp -2) (for dry grass). Specifically, for Amazon vegetation types, MEVA can improve the accuracy of daily averaged aerosol radiative forcing in the spectral range of 0.3 to 2.5 micrometers at equator at the

  5. Spatially Refined Aerosol Direct Radiative Forcing Efficiencies

    EPA Science Inventory

    Global aerosol direct radiative forcing (DRF) is an important metric for assessing potential climate impacts of future emissions changes. However, the radiative consequences of emissions perturbations are not readily quantified nor well understood at the level of detail necessary...

  6. Spatially Refined Aerosol Direct Radiative Focusing Efficiencies

    EPA Science Inventory

    Global aerosol direct radiative forcing (DRF) is an important metric for assessing potential climate impacts of future emissions changes. However, the radiative consequences of emissions perturbations are not readily quantified nor well understood at the level of detail necessary...

  7. 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.

  8. Direct Radiative Effect and Heating Rate of black carbon aerosol: high time resolution measurements and source-identified forcing effects

    NASA Astrophysics Data System (ADS)

    Ferrero, Luca; Mocnik, Grisa; Cogliati, Sergio; Comi, Alberto; Degni, Francesca; Di Mauro, Biagio; Colombo, Roberto; Bolzacchini, Ezio

    2016-04-01

    Black carbon (BC) absorbs sunlight in the atmosphere heating it. However, up to now, heating rate (HR) calculations from the divergence of the net radiative flux with altitude or from the modelling activity are too sparse. This work fills the aforementioned gap presenting a new methodology based on a full set of physical equations to experimentally determine both the radiative power density absorbed into a ground-based atmospheric layer (ADRE), and the consequent HR induced by the absorptive component of aerosol. In urban context, it is essentially related to the BC. The methodology is also applicable to natural components (i.e. dust) and is obtained solving the first derivative of the main radiative transfer equations. The ADRE and the consequent HR can be determined coupling spectral aerosol absorption measurements with the spectrally resolved measurements of the direct, diffuse downward radiation and the surface reflected radiance components. Moreover, the spectral absorption of BC aerosol allows its source apportionment (traffic and biomass burning (BB)) allowing the same apportionment on HR. This work reports one year of high-time resolution measurements (5 min) of sunlight absorption and HR induced by BC aerosol over Milan. A unique sampling site was set up from March 2015 with: 1) Aethalometer (AE-31, Magee Scientific, 7-λ), 2) the Multiplexer-Radiometer-Irradiometer which detects downward and reflected radiance (350-1000 nm in 3648 spectral bands) coupled with a rotating shadow-band to measure spectrally-resolved global and diffuse radiation (thus direct), 3) a meteorological station (LSI-Lastem) equipped with 3 pyranometers (global, diffuse and refrected radiation; 300-3000 nm), a thermohygrometer, a barometer, an anemometer, 4) condensation and optical particle counters (TSI 3775 and Grimm 1.107), 5) low volume sampler (FAI Hydra dual sampler, PM2.5 and PM10) for sample collection and chemistry determination. Results concerning the radiative power

  9. Aerosol Direct Radiative Effect at the Top of the Atmosphere Over Cloud Free Ocean Derived from Four Years of MODIS Data

    NASA Technical Reports Server (NTRS)

    Remer, L. A.; Kaufman, Y. J.

    2006-01-01

    A four year record of MODIS spaceborne data provides a new measurement tool to assess the aerosol direct radiative effect at the top of the atmosphere. MODIS derives the aerosol optical thickness and microphysical properties from the scattered sunlight at 0.55-2.1 microns. The monthly MODIS data used here are accumulated measurements across a wide range of view and scattering angles and represent the aerosol s spectrally resolved angular properties. We use these data consistently to compute with estimated accuracy of +/-0.6W/sq m the reflected sunlight by the aerosol over global oceans in cloud free conditions. The MODIS high spatial resolution (0.5 km) allows observation of the aerosol impact between clouds that can be missed by other sensors with larger footprints. We found that over the clear-sky global ocean the aerosol reflected 5.3+/-0.6W/sq m with an average radiative efficiency of 49+/-2W/sq m per unit optical thickness. The seasonal and regional distribution of the aerosol radiative effects are discussed. The analysis adds a new measurement perspective to a climate change problem dominated so far by models.

  10. Possible effect of extreme solar energetic particle event of 20 January 2005 on polar stratospheric aerosols: direct observational evidence

    NASA Astrophysics Data System (ADS)

    Mironova, I. A.; Usoskin, I. G.; Kovaltsov, G. A.; Petelina, S. V.

    2012-01-01

    Energetic cosmic rays are the main source of ionization of the low-middle atmosphere, leading to associated changes in atmospheric properties. Via the hypothetical influence of ionization on aerosol growth and facilitated formation of clouds, this may be an important indirect link relating solar variability to climate. This effect is highly debated, however, since the proposed theoretical mechanisms still remain illusive and qualitative, and observational evidence is inconclusive and controversial. Therefore, important questions regarding the existence and magnitude of the effect, and particularly the fraction of aerosol particles that can form and grow, are still open. Here we present empirical evidence of the possible effect caused by cosmic rays upon polar stratospheric aerosols, based on a case study of an extreme solar energetic particle (SEP) event of 20 January 2005. Using aerosol data obtained over polar regions from different satellites with optical instruments that were operating during January 2005, such as the Stratospheric Aerosol and Gas Experiment III (SAGE III), and Optical Spectrograph and Infrared Imaging System (OSIRIS), we found a significant simultaneous change in aerosol properties in both the Southern and Northern Polar regions in temporal association with the SEP event. We speculate that ionization of the atmosphere, which was abnormally high in the lower stratosphere during the extreme SEP event, might have led to formation of new particles and/or growth of preexisting ultrafine particles in the polar stratospheric region. However, a detailed interpretation of the effect is left for subsequent studies. This is the first time high vertical resolution measurements have been used to discuss possible production of stratospheric aerosols under the influence of cosmic ray induced ionization. The observed effect is marginally detectable for the analyzed severe SEP event and can be undetectable for the majority of weak-moderate events. The present

  11. Investigation on semi-direct and indirect climate effects of fossil fuel black carbon aerosol over China

    NASA Astrophysics Data System (ADS)

    Zhuang, Bingliang; Liu, Qian; Wang, Tijian; Yin, Changqin; Li, Shu; Xie, Min; Jiang, Fei; Mao, Huiting

    2013-11-01

    A Regional Climate Chemistry Modeling System that employed empirical parameterizations of aerosol-cloud microphysics was applied to investigate the spatial distribution, radiative forcing (RF), and climate effects of black carbon (BC) over China. Results showed high levels of BC in Southwest, Central, and East China, with maximum surface concentrations, column burden, and optical depth (AOD) up to 14 μg m-3, 8 mg m-2, and 0.11, respectively. Black carbon was found to result in a positive RF at the top of the atmosphere (TOA) due to its direct effect while a negative RF due to its indirect effect. The regional-averaged direct and indirect RF of BC in China was about +0.81 and -0.95 W m-2, respectively, leading to a net RF of -0.15 W m-2 at the TOA. The BC indirect RF was larger than its direct RF in South China. Due to BC absorption of solar radiation, cloudiness was decreased by 1.33 %, further resulting in an increase of solar radiation and subsequently a surface warming over most parts of China, which was opposite to BC's indirect effect. Further, the net effect of BC might cause a decrease of precipitation of -7.39 % over China. Investigations also suggested large uncertainties and non-linearity in BC's indirect effect on regional climate. Results suggested that: (a) changes in cloud cover might be more affected by BC's direct effect, while changes in surface air temperature and precipitation might be influenced by BC's indirect effect; and (b) BC second indirect effect might have more influence on cloud cover and water content compared to first indirect effect. This study highlighted a substantial role of BC on regional climate changes.

  12. Direct impact aerosol sampling by electrostatic precipitation

    SciTech Connect

    Braden, Jason D.; Harter, Andrew G.; Stinson, Brad J.; Sullivan, Nicholas M.

    2016-02-02

    The present disclosure provides apparatuses for collecting aerosol samples by ionizing an air sample at different degrees. An air flow is generated through a cavity in which at least one corona wire is disposed and electrically charged to form a corona therearound. At least one grounded sample collection plate is provided downstream of the at least one corona wire so that aerosol ions generated within the corona are deposited on the at least one grounded sample collection plate. A plurality of aerosol samples ionized to different degrees can be generated. The at least one corona wire may be perpendicular to the direction of the flow, or may be parallel to the direction of the flow. The apparatus can include a serial connection of a plurality of stages such that each stage is capable of generating at least one aerosol sample, and the air flow passes through the plurality of stages serially.

  13. Combining Satellite Data, Trajectory Modeling and Surface Insolation Measurements to Deduce the Direct Radiative Effect of Smoke Aerosol

    NASA Technical Reports Server (NTRS)

    Stackhouse, Paul W., Jr.; Pierce, R. Bradley; Baum, Bryan A.; DiPasquale, Robert C.

    2004-01-01

    In this paper, we have introduced a method of inferring the radiative effect of smoke aerosols using a technique that combines satellite remote sensing with trajectory modeling. The results shown here clearly show large flux biases between theoretical and measured radiative fluxes correlate with the arrival of smoke aerosol to the area. Further analysis is required to convincingly demonstrate that the reason for these differences is the radiative effect of the smoke aerosols. To do this, the estimated fluxes taken from the ERA-15 will be recomputed every 3 hours using International Satellite Cloud Climatology Project (ISCCP) data set entitled DX gridded to a 1o equal angle resolution (see paper 7B.2 for details). Surface radiometric and ancillary data for several more Canadian surface sites are being obtained at minute temporal resolution. The ultimate purpose of this research is to derive aerosol smoke maps for fire events such as this to be included in an aerosol climatology and be incorporated in the computation of the earth's surface radiation budget to better understand the radiative effect of aerosols.

  14. Impacts of global open-fire aerosols on direct radiative, cloud and surface-albedo effects simulated with CAM5

    NASA Astrophysics Data System (ADS)

    Jiang, Yiquan; Lu, Zheng; Liu, Xiaohong; Qian, Yun; Zhang, Kai; Wang, Yuhang; Yang, Xiu-Qun

    2016-11-01

    Aerosols from open-land fires could significantly perturb the global radiation balance and induce climate change. In this study, Community Atmosphere Model version 5 (CAM5) with prescribed daily fire aerosol emissions is used to investigate the spatial and seasonal characteristics of radiative effects (REs, relative to the case of no fires) of open-fire aerosols including black carbon (BC) and particulate organic matter (POM) from 2003 to 2011. The global annual mean RE from aerosol-radiation interactions (REari) of all fire aerosols is 0.16 ± 0.01 W m-2 (1σ uncertainty), mainly due to the absorption of fire BC (0.25 ± 0.01 W m-2), while fire POM induces a small effect (-0.05 and 0.04 ± 0.01 W m-2 based on two different methods). Strong positive REari is found in the Arctic and in the oceanic regions west of southern Africa and South America as a result of amplified absorption of fire BC above low-level clouds, in general agreement with satellite observations. The global annual mean RE due to aerosol-cloud interactions (REaci) of all fire aerosols is -0.70 ± 0.05 W m-2, resulting mainly from the fire POM effect (-0.59 ± 0.03 W m-2). REari (0.43 ± 0.03 W m-2) and REaci (-1.38 ± 0.23 W m-2) in the Arctic are stronger than in the tropics (0.17 ± 0.02 and -0.82 ± 0.09 W m-2 for REari and REaci), although the fire aerosol burden is higher in the tropics. The large cloud liquid water path over land areas and low solar zenith angle of the Arctic favor the strong fire aerosol REaci (up to -15 W m-2) during the Arctic summer. Significant surface cooling, precipitation reduction and increasing amounts of low-level cloud are also found in the Arctic summer as a result of the fire aerosol REaci based on the atmosphere-only simulations. The global annual mean RE due to surface-albedo changes (REsac) over land areas (0.03 ± 0.10 W m-2) is small and statistically insignificant and is mainly due to the fire BC-in-snow effect (0.02 W m-2) with the maximum albedo effect

  15. 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.

  16. Describing the direct and indirect radiative effects of atmospheric aerosols over Europe by using coupled meteorology-chemistry simulations: a contribution from the AQMEII-Phase II exercise

    NASA Astrophysics Data System (ADS)

    Jimenez-Guerrero, Pedro; Balzarini, Alessandra; Baró, Rocío; Curci, Gabriele; Forkel, Renate; Hirtl, Marcus; Honzak, Luka; Langer, Matthias; Pérez, Juan L.; Pirovano, Guido; San José, Roberto; Tuccella, Paolo; Werhahn, Johannes; Zabkar, Rahela

    2014-05-01

    The study of the response of the aerosol levels in the atmosphere to a changing climate and how this affects the radiative budget of the Earth (direct, semi-direct and indirect effects) is an essential topic to build confidence on climate science, since these feedbacks involve the largest uncertainties nowadays. Air quality-climate interactions (AQCI) are, therefore, a key, but uncertain contributor to the anthropogenic forcing that remains poorly understood. To build confidence in the AQCI studies, regional-scale integrated meteorology-atmospheric chemistry models (i.e., models with on-line chemistry) that include detailed treatment of aerosol life cycle and aerosol impacts on radiation (direct effects) and clouds (indirect effects) are in demand. In this context, the main objective of this contribution is the study and definition of the uncertainties in the climate-chemistry-aerosol-cloud-radiation system associated to the direct radiative forcing and the indirect effect caused by aerosols over Europe, using an ensemble of fully-coupled meteorology-chemistry model simulations with the WRF-Chem model run under the umbrella of AQMEII-Phase 2 international initiative. Simulations were performed for Europe for the entire year 2010. According to the common simulation strategy, the year was simulated as a sequence of 2-day time slices. For better comparability, the seven groups applied the same grid spacing of 23 km and shared common processing of initial and boundary conditions as well as anthropogenic and fire emissions. With exception of a simulation with different cloud microphysics, identical physics options were chosen while the chemistry options were varied. Two model set-ups will be considered here: one sub-ensemble of simulations not taking into account any aerosol feedbacks (the baseline case) and another sub-ensemble of simulations which differs from the former by the inclusion of aerosol-radiation feedback. The existing differences for meteorological

  17. A Novel Method for Estimating Shortwave Direct Radiative Effect of Above-cloud Aerosols over Ocean Using CALIOP and MODIS Data

    NASA Technical Reports Server (NTRS)

    Zhang, Z.; Meyer, K.; Platnick, S.; Oreopoulos, L.; Lee, D.; Yu, H.

    2013-01-01

    This paper describes an efficient and unique method for computing the shortwave direct radiative effect (DRE) of aerosol residing above low-level liquid-phase clouds using CALIOP and MODIS data. It accounts for the overlapping of aerosol and cloud rigorously by utilizing the joint histogram of cloud optical depth and cloud top pressure. Effects of sub-grid scale cloud and aerosol variations on DRE are accounted for. It is computationally efficient through using grid-level cloud and aerosol statistics, instead of pixel-level products, and a pre-computed look-up table in radiative transfer calculations. We verified that for smoke over the southeast Atlantic Ocean the method yields a seasonal mean instantaneous shortwave DRE that generally agrees with more rigorous pixel-level computation within 4%. We have also computed the annual mean instantaneous shortwave DRE of light-absorbing aerosols (i.e., smoke and polluted dust) over global ocean based on 4 yr of CALIOP and MODIS data. We found that the variability of the annual mean shortwave DRE of above-cloud light-absorbing aerosol is mainly driven by the optical depth of the underlying clouds.

  18. An assessment of the quality of aerosol retrievals over the Red Sea and evaluation of the climatological cloud-free dust direct radiative effect in the region

    NASA Astrophysics Data System (ADS)

    Brindley, H.; Osipov, S.; Bantges, R.; Smirnov, A.; Banks, J.; Levy, R.; Jish Prakash, P.; Stenchikov, G.

    2015-10-01

    Ground-based and satellite observations are used in conjunction with the Rapid Radiative Transfer Model (RRTM) to assess climatological aerosol loading and the associated cloud-free aerosol direct radiative effect (DRE) over the Red Sea. Aerosol optical depth (AOD) retrievals from the Moderate Resolution Imaging Spectroradiometer and Spinning Enhanced Visible and InfraRed Imager (SEVIRI) instruments are first evaluated via comparison with ship-based observations. Correlations are typically better than 0.9 with very small root-mean-square and bias differences. Calculations of the DRE along the ship cruises using RRTM also show good agreement with colocated estimates from the Geostationary Earth Radiation Budget instrument if the aerosol asymmetry parameter is adjusted to account for the presence of large particles. A monthly climatology of AOD over the Red Sea is then created from 5 years of SEVIRI retrievals. This shows enhanced aerosol loading and a distinct north to south gradient across the basin in the summer relative to the winter months. The climatology is used with RRTM to estimate the DRE at the top and bottom of the atmosphere and the atmospheric absorption due to dust aerosol. These climatological estimates indicate that although longwave effects can reach tens of W m-2, shortwave cooling typically dominates the net radiative effect over the Sea, being particularly pronounced in the summer, reaching 120 W m-2 at the surface. The spatial gradient in summertime AOD is reflected in the radiative effect at the surface and in associated differential heating by aerosol within the atmosphere above the Sea. This asymmetric effect is expected to exert a significant influence on the regional atmospheric and oceanic circulation.

  19. Possible effect of extreme solar energetic particle event of 20 January 2005 on polar stratospheric aerosols: direct observational evidence

    NASA Astrophysics Data System (ADS)

    Mironova, I. A.; Usoskin, I. G.; Kovaltsov, G. A.; Petelina, S. V.

    2011-05-01

    Energetic cosmic rays are the main source of ionization of the low-middle atmosphere, leading to associated changes in atmospheric properties. Via the hypothetical influence of ionization on aerosol growth and facilitated formation of cloud condensation nuclei, this may be an important indirect link relating solar variability to climate. This effect is highly debated, however, since the proposed theoretical mechanisms still remain illusive and qualitative, and observational evidence is inconclusive and controversial. Therefore, important questions regarding the existence and magnitude of the effect, and particularly the fraction of aerosol particles that can be formed and grow large enough to influence cloud condensation nuclei (CCN), are still open. Here we present empirical evidence of the possible effect caused by cosmic rays upon polar stratospheric aerosols, based on a case study of an extreme solar energetic particle (SEP) event of 20 January 2005. Using aerosol data obtained over polar regions from different satellites with optical instruments that were operating during January 2005, such as the Stratospheric Aerosol and Gas Experiment III (SAGE III), and Optical Spectrograph and Infrared Imaging System (OSIRIS), we found a significant simultaneous change in aerosol properties in both the southern and northern polar regions in temporal association with the SEP event. We speculate that ionization of the atmosphere, which was abnormally high during this extreme SEP event, might have led to formation of new particles and/or growth of preexisting ultrafine particles up to the size of CCN. However, a detailed interpretation of the effect is left for subsequent studies. This is the first time high vertical resolution measurements have been used to provide evidence for the probable production of stratospheric CCN from cosmic ray induced ionization.

  20. Aerosol Direct, Indirect, Semidirect, and Surface Albedo Effects from Sector Contributions Based on the IPCC AR5 Emissions for Preindustrial and Present-day Conditions

    NASA Technical Reports Server (NTRS)

    Bauer, Susanne E.; Menon, Surabi

    2012-01-01

    The anthropogenic increase in aerosol concentrations since preindustrial times and its net cooling effect on the atmosphere is thought to mask some of the greenhouse gas-induced warming. Although the overall effect of aerosols on solar radiation and clouds is most certainly negative, some individual forcing agents and feedbacks have positive forcing effects. Recent studies have tried to identify some of those positive forcing agents and their individual emission sectors, with the hope that mitigation policies could be developed to target those emitters. Understanding the net effect of multisource emitting sectors and the involved cloud feedbacks is very challenging, and this paper will clarify forcing and feedback effects by separating direct, indirect, semidirect and surface albedo effects due to aerosols. To this end, we apply the Goddard Institute for Space Studies climate model including detailed aerosol microphysics to examine aerosol impacts on climate by isolating single emission sector contributions as given by the Coupled Model Intercomparison Project Phase 5 (CMIP5) emission data sets developed for Intergovernmental Panel on Climate Change (IPCC) AR5. For the modeled past 150 years, using the climate model and emissions from preindustrial times to present-day, the total global annual mean aerosol radiative forcing is -0.6 W/m(exp 2), with the largest contribution from the direct effect (-0.5 W/m(exp 2)). Aerosol-induced changes on cloud cover often depends on cloud type and geographical region. The indirect (includes only the cloud albedo effect with -0.17 W/m(exp 2)) and semidirect effects (-0.10 W/m(exp 2)) can be isolated on a regional scale, and they often have opposing forcing effects, leading to overall small forcing effects on a global scale. Although the surface albedo effects from aerosols are small (0.016 W/m(exp 2)), triggered feedbacks on top of the atmosphere (TOA) radiative forcing can be 10 times larger. Our results point out that each

  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. 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.

  3. Indirect and semi-direct aerosol campaign: The impact of Arctic aerosols on clouds

    SciTech Connect

    McFarquhar, Greg M.; Ghan, Steven; Verlinde, Johannes; Korolev, Alexei; Strapp, J. Walter; Schmid, Beat; Tomlinson, Jason M.; Wolde, Menqistu; Brooks, Sarah D.; Cziczo, Dan; Dubey, Manvendra K.; Fan, Jiwen; Flynn, Connor; Gultepe, Ismail; Hubbe, John; Gilles, Mary K.; Laskin, Alexander; Lawson, Paul; Leaitch, W. Richard; Liu, Peter; Liu, Xiaohong; Lubin, Dan; Mazzoleni, Claudio; Macdonald, Ann -Marie; Moffet, Ryan C.; Morrison, Hugh; Ovchinnikov, Mikhail; Ronfeld, Debbie; Shupe, Matthew D.; Xie, Shaocheng; Zelenyuk, Alla; Bae, Kenny; Freer, Matt; Glen, Andrew

    2011-02-01

    A comprehensive dataset of microphysical and radiative properties of aerosols and clouds in the boundary layer in the vicinity of Barrow, Alaska, was collected in April 2008 during the Indirect and Semi-Direct Aerosol Campaign (ISDAC). ISDAC's primary aim was to examine the effects of aerosols, including those generated by Asian wildfires, on clouds that contain both liquid and ice. ISDAC utilized the Atmospheric Radiation Measurement Pro- gram's permanent observational facilities at Barrow and specially deployed instruments measuring aerosol, ice fog, precipitation, and radiation. The National Research Council of Canada Convair-580 flew 27 sorties and collected data using an unprecedented 41 stateof- the-art cloud and aerosol instruments for more than 100 h on 12 different days. Aerosol compositions, including fresh and processed sea salt, biomassburning particles, organics, and sulfates mixed with organics, varied between flights. Observations in a dense arctic haze on 19 April and above, within, and below the single-layer stratocumulus on 8 and 26 April are enabling a process-oriented understanding of how aerosols affect arctic clouds. Inhomogeneities in reflectivity, a close coupling of upward and downward Doppler motion, and a nearly constant ice profile in the single-layer stratocumulus suggests that vertical mixing is responsible for its longevity observed during ISDAC. Data acquired in cirrus on flights between Barrow and Fairbanks, Alaska, are improving the understanding of the performance of cloud probes in ice. Furthermore, ISDAC data will improve the representation of cloud and aerosol processes in models covering a variety of spatial and temporal scales, and determine the extent to which surface measurements can provide retrievals of aerosols, clouds, precipitation, and radiative heating.

  4. Indirect and semi-direct aerosol campaign: The impact of Arctic aerosols on clouds

    DOE PAGES

    McFarquhar, Greg M.; Ghan, Steven; Verlinde, Johannes; ...

    2011-02-01

    A comprehensive dataset of microphysical and radiative properties of aerosols and clouds in the boundary layer in the vicinity of Barrow, Alaska, was collected in April 2008 during the Indirect and Semi-Direct Aerosol Campaign (ISDAC). ISDAC's primary aim was to examine the effects of aerosols, including those generated by Asian wildfires, on clouds that contain both liquid and ice. ISDAC utilized the Atmospheric Radiation Measurement Pro- gram's permanent observational facilities at Barrow and specially deployed instruments measuring aerosol, ice fog, precipitation, and radiation. The National Research Council of Canada Convair-580 flew 27 sorties and collected data using an unprecedented 41more » stateof- the-art cloud and aerosol instruments for more than 100 h on 12 different days. Aerosol compositions, including fresh and processed sea salt, biomassburning particles, organics, and sulfates mixed with organics, varied between flights. Observations in a dense arctic haze on 19 April and above, within, and below the single-layer stratocumulus on 8 and 26 April are enabling a process-oriented understanding of how aerosols affect arctic clouds. Inhomogeneities in reflectivity, a close coupling of upward and downward Doppler motion, and a nearly constant ice profile in the single-layer stratocumulus suggests that vertical mixing is responsible for its longevity observed during ISDAC. Data acquired in cirrus on flights between Barrow and Fairbanks, Alaska, are improving the understanding of the performance of cloud probes in ice. Furthermore, ISDAC data will improve the representation of cloud and aerosol processes in models covering a variety of spatial and temporal scales, and determine the extent to which surface measurements can provide retrievals of aerosols, clouds, precipitation, and radiative heating.« less

  5. Estimating the Direct Radiative Effect of Absorbing Aerosols Overlying Marine Boundary Layer Clouds in the Southeast Atlantic Using MODIS and CALIOP

    NASA Technical Reports Server (NTRS)

    Meyer, Kerry; Platnick, Steven; Oreopoulos, Lazaros; Lee, Dongmin

    2013-01-01

    Absorbing aerosols such as smoke strongly absorb solar radiation, particularly at ultraviolet and visible/near-infrared (VIS/NIR) wavelengths, and their presence above clouds can have considerable implications. It has been previously shown that they have a positive (i.e., warming) direct aerosol radiative effect (DARE) when overlying bright clouds. Additionally, they can cause biased passive instrument satellite retrievals in techniques that rely on VIS/NIR wavelengths for inferring the cloud optical thickness (COT) and effective radius (re) of underlying clouds, which can in turn yield biased above-cloud DARE estimates. Here we investigate Moderate Resolution Imaging Spectroradiometer (MODIS) cloud optical property retrieval biases due to overlying absorbing aerosols observed by Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP) and examine the impact of these biases on above-cloud DARE estimates. The investigation focuses on a region in the southeast Atlantic Ocean during August and September (2006-2011), where smoke from biomass burning in southern Africa overlies persistent marine boundary layer stratocumulus clouds. Adjusting for above-cloud aerosol attenuation yields increases in the regional mean liquid COT (averaged over all ocean-only liquid clouds) by roughly 6%; mean re increases by roughly 2.6%, almost exclusively due to the COT adjustment in the non-orthogonal retrieval space. It is found that these two biases lead to an underestimate of DARE. For liquid cloud Aqua MODIS pixels with CALIOP-observed above-cloud smoke, the regional mean above-cloud radiative forcing efficiency (DARE per unit aerosol optical depth (AOD)) at time of observation (near local noon for Aqua overpass) increases from 50.9Wm(sup-2)AOD(sup-1) to 65.1Wm(sup-2)AOD(sup -1) when using bias-adjusted instead of nonadjusted MODIS cloud retrievals.

  6. Impacts of global open-fire aerosols on direct radiative, cloud and surface-albedo effects simulated with CAM5

    SciTech Connect

    Jiang, Yiquan; Lu, Zheng; Liu, Xiaohong; Qian, Yun; Zhang, Kai; Wang, Yuhang; Yang, Xiu-Qun

    2016-11-29

    Aerosols from open-land fires could significantly perturb the global radiation balance and induce climate change. In this study, Community Atmosphere Model version 5 (CAM5) with prescribed daily fire aerosol emissions is used to investigate the spatial and seasonal characteristics of radiative effects (REs, relative to the case of no fires) of open-fire aerosols including black carbon (BC) and particulate organic matter (POM) from 2003 to 2011. The global annual mean RE from aerosol–radiation interactions (REari) of all fire aerosols is 0.16 ± 0.01 W m-2 (1σ uncertainty), mainly due to the absorption of fire BC (0.25 ± 0.01 W m-2), while fire POM induces a small effect (-0.05 and 0.04 ± 0.01 W m-2 based on two different methods). Strong positive REari is found in the Arctic and in the oceanic regions west of southern Africa and South America as a result of amplified absorption of fire BC above low-level clouds, in general agreement with satellite observations. The global annual mean RE due to aerosol–cloud interactions (REaci) of all fire aerosols is -0.70 ± 0.05 W m-2, resulting mainly from the fire POM effect (-0.59 ± 0.03 W m-2). REari (0.43 ± 0.03 W m-2) and REaci (-1.38 ± 0.23 W m-2) in the Arctic are stronger than in the tropics (0.17 ± 0.02 and -0.82 ± 0.09 W m-2 for REari and REaci), although the fire aerosol burden is higher in the tropics. The large cloud liquid water path over land areas and low solar zenith angle of the Arctic favor the strong fire aerosol REaci (up to -15 Wm-2) during the Arctic summer. Significant surface cooling, precipitation reduction and increasing amounts of low-level cloud are also found in the Arctic summer as a result of the fire aerosol REaci based on the atmosphere-only simulations. The global annual mean RE due to surface-albedo changes (REsac) over land areas (0.03 ± 0.10 W m-2) is small

  7. Impacts of global open-fire aerosols on direct radiative, cloud and surface-albedo effects simulated with CAM5

    DOE PAGES

    Jiang, Yiquan; Lu, Zheng; Liu, Xiaohong; ...

    2016-11-29

    Aerosols from open-land fires could significantly perturb the global radiation balance and induce climate change. In this study, Community Atmosphere Model version 5 (CAM5) with prescribed daily fire aerosol emissions is used to investigate the spatial and seasonal characteristics of radiative effects (REs, relative to the case of no fires) of open-fire aerosols including black carbon (BC) and particulate organic matter (POM) from 2003 to 2011. The global annual mean RE from aerosol–radiation interactions (REari) of all fire aerosols is 0.16 ± 0.01 W m−2 (1σ uncertainty), mainly due to the absorption of fire BC (0.25 ± 0.01 W m−2), while fire POM induces a small effect (−0.05 andmore » 0.04 ± 0.01 W m−2 based on two different methods). Strong positive REari is found in the Arctic and in the oceanic regions west of southern Africa and South America as a result of amplified absorption of fire BC above low-level clouds, in general agreement with satellite observations. The global annual mean RE due to aerosol–cloud interactions (REaci) of all fire aerosols is −0.70 ± 0.05 W m−2, resulting mainly from the fire POM effect (−0.59 ± 0.03 W m−2). REari (0.43 ± 0.03 W m−2) and REaci (−1.38 ± 0.23 W m−2) in the Arctic are stronger than in the tropics (0.17 ± 0.02 and −0.82 ± 0.09 W m−2 for REari and REaci), although the fire aerosol burden is higher in the tropics. The large cloud liquid water path over land areas and low solar zenith angle of the Arctic favor the strong fire aerosol REaci (up to −15 W m−2) during the Arctic summer. Significant surface cooling, precipitation reduction and increasing amounts of low-level cloud are also found in the Arctic summer as a result of the fire aerosol REaci based on the atmosphere-only simulations. The global annual mean RE due to surface-albedo changes (REsac) over land areas (0.03 ± 0.10 W m−2) is small

  8. 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.

  9. Assessment of multi-decadal WRF-CMAQ simulations for understanding direct aerosol effects on radiation "brightening" in the United States

    NASA Astrophysics Data System (ADS)

    Gan, C.-M.; Pleim, J.; Mathur, R.; Hogrefe, C.; Long, C. N.; Xing, J.; Wong, D.; Gilliam, R.; Wei, C.

    2015-07-01

    Multi-decadal simulations with the coupled WRF-CMAQ model have been conducted to systematically investigate the changes in anthropogenic emissions of SO2 and NOx over the past 21 years (1990-2010) across the United States (US), their impacts on anthropogenic aerosol loading over North America, and subsequent impacts on regional radiation budgets. In particular, this study attempts to determine the consequences of the changes in tropospheric aerosol burden arising from substantial reductions in emissions of SO2 and NOx associated with control measures under the Clean Air Act (CAA) especially on trends in solar radiation. Extensive analyses conducted by Gan et al. (2014) utilizing observations (e.g. SURFRAD, CASTNET, IMPROVE and ARM) over the past 16 years (1995-2010) indicate a shortwave (SW) radiation (both all-sky and clear-sky) "brightening" in the US. The relationship of the radiation brightening trend with decreases in the aerosol burden is less apparent in the western US. One of the main reasons for this is that the emission controls under the CAA were aimed primarily at reducing pollutants in areas violating national air quality standards, most of which were located in the eastern US while the relatively less populated areas in the western US were less polluted at the beginning of this study period. Comparisons of model results with observations of aerosol optical depth (AOD), aerosol concentration, and radiation demonstrate that the coupled WRF-CMAQ model is capable of replicating the trends well even through it tends to underestimate the AOD. In particular, the sulfate concentration predictions were well matched with the observations. The discrenpancies found in the clear-sky diffuse SW radiation are likely due to several factors such as potential increase of ice particles associated with increasing air traffic, the definition of "clear-sky" in the radiation retrieval methodology and aerosol semi-direct and/or indirect effects which cannot be readily

  10. Air pollution and climate response to aerosol direct radiative ...

    EPA Pesticide Factsheets

    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 surface temperature, relative humidity, wind speed, and direction was evaluated through comparison with observations from NOAA's National Climatic Data Center Integrated Surface Data. The inclusion of aerosol direct radiative effects improves the model's ability to reproduce the trend in daytime temperature range which over the past two decades was increasing in eastern China but decreasing in eastern U.S. and Europe. Trends and spatial and diurnal variations of the surface-level gaseous and particle concentrations to the aerosol direct effect were analyzed. The inclusion of aerosol direct radiative effects was found to increase the surface-level concentrations of SO2, NO2, O3, SO42−, NO3−, and particulate matter 2.5 in eastern China, eastern U.S., and Europe by 1.5–2.1%, 1–1.5%, 0.1–0.3%, 1.6–2.3%, 3.5–10.0%, and 2.2–3.2%, respectively, on average over the entire 21 year period. However, greater impacts are noted during polluted days with increases of 7.6–10.6%, 6.2–6.7%, 2.0–3.0%, 7.8–9.5%, 11.1–18.6%, and 7.2–10.1%, respectively. Due to the aerosol direct radiative effects, stabilizing of the atmosphere associated with reduced planetary boundary layer height a

  11. Indirect and Semi-Direct Aerosol Campaign: The Impact of Arctic Aerosols on Clouds

    SciTech Connect

    McFarquhar, Greg; Ghan, Steven J.; Verlinde, J.; Korolev, Alexei; Strapp, J. Walter; Schmid, Beat; Tomlinson, Jason M.; Wolde, Mengistu; Brooks, Sarah D.; Cziczo, Daniel J.; Dubey, Manvendra K.; Fan, Jiwen; Flynn, Connor J.; Gultepe, Ismail; Hubbe, John M.; Gilles, Mary K.; Laskin, Alexander; Lawson, Paul; Leaitch, W. R.; Liu, Peter S.; Liu, Xiaohong; Lubin, Dan; Mazzoleni, Claudio; Macdonald, A. M.; Moffet, Ryan C.; Morrison, H.; Ovchinnikov, Mikhail; Shupe, Matthew D.; Turner, David D.; Xie, Shaocheng; Zelenyuk, Alla; Bae, Kenny; Freer, Matthew; Glen, Andrew

    2011-02-01

    A comprehensive dataset of microphysical and radiative properties of aerosols and clouds in the arctic boundary layer in the vicinity of Barrow, Alaska was collected in April 2008 during the Indirect and Semi-Direct Aerosol Campaign (ISDAC) sponsored by the Department of Energy Atmospheric Radiation Measurement (ARM) and Atmospheric Science Programs. The primary aim of ISDAC was to examine indirect effects of aerosols on clouds that contain both liquid and ice water. The experiment utilized the ARM permanent observational facilities at the North Slope of Alaska (NSA) in Barrow. These include a cloud radar, a polarized micropulse lidar, and an atmospheric emitted radiance interferometer as well as instruments specially deployed for ISDAC measuring aerosol, ice fog, precipitation and spectral shortwave radiation. The National Research Council of Canada Convair-580 flew 27 sorties during ISDAC, collecting data using an unprecedented 42 cloud and aerosol instruments for more than 100 hours on 12 different days. Data were obtained above, below and within single-layer stratus on 8 April and 26 April 2008. These data enable a process-oriented understanding of how aerosols affect the microphysical and radiative properties of arctic clouds influenced by different surface conditions. Observations acquired on a heavily polluted day, 19 April 2008, are enhancing this understanding. Data acquired in cirrus on transit flights between Fairbanks and Barrow are improving our understanding of the performance of cloud probes in ice. Ultimately the ISDAC data will be used to improve the representation of cloud and aerosol processes in models covering a variety of spatial and temporal scales, and to determine the extent to which long-term surface-based measurements can provide retrievals of aerosols, clouds, precipitation and radiative heating in the Arctic.

  12. Direct Aerosol Radiative Forcing: Calculations and Measurements from the Tropospheric

    NASA Technical Reports Server (NTRS)

    Russell, P. B.; Hignett, P.; Stowe, L. L.; Livingston, J. M.; Kinne, S.; Wong, J.; Chan, K. Roland (Technical Monitor)

    1997-01-01

    Radiative forcing is defined as the change in the net (downwelling minus upwelling) radiative flux at a given level in the atmosphere. This net flux is the radiative power density available to drive climatic processes in the earth-atmosphere system below that level. Recent research shows that radiative forcing by aerosol particles is a major source of uncertainty in climate predictions. To reduce those uncertainties, TARFOX was designed to determine direct (cloud-free) radiative forcing by the aerosols in one of the world's major industrial pollution plumes--that flowing from the east coast of the US over the Atlantic Ocean. TARFOX measured a variety of aerosol radiative effects (including direct forcing) while simultaneously measuring the chemical, physical, and optical properties of the aerosol particles causing those effects. The resulting data sets permit a wide variety of tests of the consistency, or closure, among the measurements and the models that link them. Because climate predictions use the same or similar model components, closure tests help to assess and reduce prediction uncertainties. In this work we use the TARFOX-determined aerosol, gas, and surface properties to compute radiative forcing for a variety of aerosol episodes, with inadvisable optical depths ranging from 0.07 to 0.6. We calculate forcing by several techniques with varying degrees of sophistication, in part to test the range of applicability of simplified techniques--which are often the only ones feasible in climate predictions by general circulation models (GCMs). We then compare computed forcing to that determined from: (1) Upwelling and downwelling fluxes (0.3-0.7 mm and 0.7-3.0 mm) measured by radiometers on the UK MRF C-130. and (2) Daily average cloud-free absorbed solar and emitted thermal radiative flux at the top of the atmosphere derived from the AVHRR radiometer on the NOAA- 14 satellite. The calculations and measurements all yield aerosol direct radiative forcing in the

  13. Evaluation of multidecadal variability in CMIP5 surface solar radiation and inferred underestimation of aerosol direct effects over Europe, China, Japan, and India

    NASA Astrophysics Data System (ADS)

    Allen, R. J.; Norris, J. R.; Wild, M.

    2013-06-01

    Observations from the Global Energy Balance Archive indicate regional decreases in all sky surface solar radiation from ˜1950s to 1980s, followed by an increase during the 1990s. These periods are popularly called dimming and brightening, respectively. Removal of the radiative effects of cloud cover variability from all sky surface solar radiation results in a quantity called "clear sky proxy" radiation, in which multidecadal trends can be seen more distinctly, suggesting aerosol radiative forcing as a likely cause. Prior work has shown climate models from the Coupled Model Intercomparison Project 3 (CMIP3) generally underestimate the magnitude of these trends, particularly over China and India. Here we perform a similar analysis with 173 simulations from 42 climate models participating in the new CMIP5. Results show negligible improvement over CMIP3, as CMIP5 dimming trends over four regions—Europe, China, India, and Japan—are all underestimated. This bias is largest for both India and China, where the multimodel mean yields a decrease in clear sky proxy radiation of -1.3±0.3 and -1.2±0.2 W m-2decade-1, respectively, compared to observed decreases of -6.5±0.9 and -8.2±1.3 W m-2decade-1. Similar underestimation of the observed dimming over Japan exists, with the CMIP5 mean dimming ˜20% as large as observed. Moreover, not a single simulation reproduces the magnitude of the observed dimming trend for these three regions. Relative to dimming, CMIP5 models better simulate the observed brightening, but significant underestimation exists for both China and Japan. Overall, no individual model performs particularly well for all four regions. Model biases do not appear to be related to the use of prescribed versus prognostic aerosols or to aerosol indirect effects. However, models exhibit significant correlations between clear sky proxy radiation and several aerosol-related fields, most notably aerosol optical depth (AOD) and absorption AOD. This suggests model

  14. Shortwave direct radiative effects of above-cloud aerosols over global oceans derived from 8 years of CALIOP and MODIS observations

    NASA Astrophysics Data System (ADS)

    Zhang, Zhibo; Meyer, Kerry; Yu, Hongbin; Platnick, Steven; Colarco, Peter; Liu, Zhaoyan; Oreopoulos, Lazaros

    2016-03-01

    In this paper, we studied the frequency of occurrence and shortwave direct radiative effects (DREs) of above-cloud aerosols (ACAs) over global oceans using 8 years (2007-2014) of collocated CALIOP and MODIS observations. Similar to previous work, we found high ACA occurrence in four regions: southeastern (SE) Atlantic region, where ACAs are mostly light-absorbing aerosols, i.e., smoke and polluted dust according to CALIOP classification, originating from biomass burning over the African Savanna; tropical northeastern (TNE) Atlantic and the Arabian Sea, where ACAs are predominantly windblown dust from the Sahara and Arabian deserts, respectively; and the northwestern (NW) Pacific, where ACAs are mostly transported smoke and polluted dusts from Asian. From radiative transfer simulations based on CALIOP-MODIS observations and a set of the preselected aerosol optical models, we found the DREs of ACAs at the top of atmosphere (TOA) to be positive (i.e., warming) in the SE Atlantic and NW Pacific regions, but negative (i.e., cooling) in the TNE Atlantic Ocean and the Arabian Sea. The cancellation of positive and negative regional DREs results in a global ocean annual mean diurnally averaged cloudy-sky DRE of 0.015 W m-2 (range of -0.03 to 0.06 W m-2) at TOA. The DREs at surface and within the atmosphere are -0.15 W m-2 (range of -0.09 to -0.21 W m-2), and 0.17 W m-2 (range of 0.11 to 0.24 W m-2), respectively. The regional and seasonal mean DREs are much stronger. For example, in the SE Atlantic region, the JJA (July-August) seasonal mean cloudy-sky DRE is about 0.7 W m-2 (range of 0.2 to 1.2 W m-2) at TOA. All our DRE computations are publicly available1. The uncertainty in our DRE computations is mainly caused by the uncertainties in the aerosol optical properties, in particular aerosol absorption, the uncertainties in the CALIOP operational aerosol optical thickness retrieval, and the ignorance of cloud and potential aerosol diurnal cycle. In situ and remotely sensed

  15. The impact of the direct effects of sulfate and black carbon aerosols on the subseasonal march of the East Asian subtropical summer monsoon

    NASA Astrophysics Data System (ADS)

    Wang, Dongdong; Zhu, Bin; Jiang, Zhihong; Yang, Xiu-Qun; Zhu, Tong

    2016-03-01

    Aerosol emissions have rapidly increased in East Asia since the late 1970s. During the same period, the East Asian summer monsoon has shown a weakening trend. In this work, the direct effects (DE) of sulfate and black carbon (BC) aerosols on the subseasonal (pentad mean) march of the East Asian subtropical summer monsoon (EASSM) are investigated using an interactive global climate-chemistry model. The simulation results suggest that the DE of sulfate aerosols have a notable effect on the cooling of the low troposphere across the continent in spring and autumn, hence, changing the time of the seasonal transition of the zonal land-sea thermal contrast (ZTC). The DE of BC result in cooling of the low troposphere and heating of the middle troposphere, leading to a different impact than that caused by sulfates. The cooling of the surface and troposphere by sulfates leads to a delay in the warming of East Asian continent in spring and the EASSM onset time; it also accelerates the process of the continent turning colder and advances the retreat of the EASSM. The deeper heating in the middle-upper troposphere than the cooling in the low troposphere due to the DE of BC or the combination of both lead to an advance in the onset time of the monsoon caused by the continent turning warmer earlier in spring. In autumn, the same cooling effect by sulfates leads to the continent turning colder earlier, resulting in an advance in the retreat time.

  16. In vitro exposure to isoprene-derived secondary organic aerosol by direct deposition and its effects on COX-2 and IL-8 gene expression

    NASA Astrophysics Data System (ADS)

    Arashiro, Maiko; Lin, Ying-Hsuan; Sexton, Kenneth G.; Zhang, Zhenfa; Jaspers, Ilona; Fry, Rebecca C.; Vizuete, William G.; Gold, Avram; Surratt, Jason D.

    2016-11-01

    Atmospheric oxidation of isoprene, the most abundant non-methane hydrocarbon emitted into Earth's atmosphere primarily from terrestrial vegetation, is now recognized as a major contributor to the global secondary organic aerosol (SOA) burden. Anthropogenic pollutants significantly enhance isoprene SOA formation through acid-catalyzed heterogeneous chemistry of epoxide products. Since isoprene SOA formation as a source of fine aerosol is a relatively recent discovery, research is lacking on evaluating its potential adverse effects on human health. The objective of this study was to examine the effect of isoprene-derived SOA on inflammation-associated gene expression in human lung cells using a direct deposition exposure method. We assessed altered expression of inflammation-related genes in human bronchial epithelial cells (BEAS-2B) exposed to isoprene-derived SOA generated in an outdoor chamber facility. Measurements of gene expression of known inflammatory biomarkers interleukin 8 (IL-8) and cyclooxygenase 2 (COX-2) in exposed cells, together with complementary chemical measurements, showed that a dose of 0.067 µg cm-2 of SOA from isoprene photooxidation leads to statistically significant increases in IL-8 and COX-2 mRNA levels. Resuspension exposures using aerosol filter extracts corroborated these findings, supporting the conclusion that isoprene-derived SOA constituents induce the observed changes in mRNA levels. The present study is an attempt to examine the early biological responses of isoprene SOA exposure in human lung cells.

  17. Aerosol effects on deep convective clouds: impact of changes in aerosol size distribution and aerosol activation parameterization

    NASA Astrophysics Data System (ADS)

    Ekman, A. M. L.; Engström, A.; Söderberg, A.

    2010-03-01

    A cloud-resolving model including explicit aerosol physics and chemistry is used to study the impact of aerosols on deep convective strength. More specifically, by conducting six sensitivity series we examine how the complexity of the aerosol model, the size of the aerosols and the aerosol activation parameterization influence the aerosol-induced deep convective cloud sensitivity. Only aerosol effects on liquid droplet formation are considered. We find that an increased aerosol concentration generally results in stronger convection, which for the simulated case is in agreement with the conceptual model presented by Rosenfeld et al. (2008). However, there are two sensitivity series that do not display a monotonic increase in updraft velocity with increasing aerosol concentration. These exceptions illustrate the need to: 1) account for changes in evaporation processes and subsequent cooling when assessing aerosol effects on deep convective strength, 2) better understand graupel impaction scavenging of aerosols which may limit the number of CCN at a critical stage of cloud development and thereby dampen the convection, 3) increase our knowledge of aerosol recycling due to evaporation of cloud droplets. Furthermore, we find a significant difference in the aerosol-induced deep convective cloud sensitivity when using different complexities of the aerosol model and different aerosol activation parameterizations. For the simulated case, a 100% increase in aerosol concentration results in a difference in average updraft between the various sensitivity series which is as large as the average updraft increase itself. The model simulations also show that the change in graupel and rain formation is not necessarily directly proportional to the change in updraft velocity. For example, several of the sensitivity series display a decrease of the rain amount at the lowest model level with increasing updraft velocity. Finally, an increased number of aerosols in the Aitken mode (here

  18. CATS Aerosol Typing and Future Directions

    NASA Technical Reports Server (NTRS)

    McGill, Matt; Yorks, John; Scott, Stan; Palm, Stephen; Hlavka, Dennis; Hart, William; Nowottnick, Ed; Selmer, Patrick; Kupchock, Andrew; Midzak, Natalie; Trepte, Chip; Vaughan, Mark; Colarco, Peter; da Silva, Arlindo

    2016-01-01

    The Cloud Aerosol Transport System (CATS), launched in January of 2015, is a lidar remote sensing instrument that will provide range-resolved profile measurements of atmospheric aerosols and clouds from the International Space Station (ISS). CATS is intended to operate on-orbit for at least six months, and up to three years. Status of CATS Level 2 and Plans for the Future:Version. 1. Aerosol Typing (ongoing): Mode 1: L1B data released later this summer; L2 data released shortly after; Identify algorithm biases (ex. striping, FOV (field of view) biases). Mode 2: Processed Released Currently working on correcting algorithm issues. Version 2 Aerosol Typing (Fall, 2016): Implementation of version 1 modifications Integrate GEOS-5 aerosols for typing guidance for non spherical aerosols. Version 3 Aerosol Typing (2017): Implementation of 1-D Var Assimilation into GEOS-5 Dynamic lidar ratio that will evolve in conjunction with simulated aerosol mixtures.

  19. Spatially Refined Aerosol Direct Radiative Forcing Efficiencies

    NASA Technical Reports Server (NTRS)

    Henze, Daven K.; Shindell, Drew Todd; Akhtar, Farhan; Spurr, Robert J. D.; Pinder, Robert W.; Loughlin, Dan; Kopacz, Monika; Singh, Kumaresh; Shim, Changsub

    2012-01-01

    Global aerosol direct radiative forcing (DRF) is an important metric for assessing potential climate impacts of future emissions changes. However, the radiative consequences of emissions perturbations are not readily quantified nor well understood at the level of detail necessary to assess realistic policy options. To address this challenge, here we show how adjoint model sensitivities can be used to provide highly spatially resolved estimates of the DRF from emissions of black carbon (BC), primary organic carbon (OC), sulfur dioxide (SO2), and ammonia (NH3), using the example of emissions from each sector and country following multiple Representative Concentration Pathway (RCPs). The radiative forcing efficiencies of many individual emissions are found to differ considerably from regional or sectoral averages for NH3, SO2 from the power sector, and BC from domestic, industrial, transportation and biomass burning sources. Consequently, the amount of emissions controls required to attain a specific DRF varies at intracontinental scales by up to a factor of 4. These results thus demonstrate both a need and means for incorporating spatially refined aerosol DRF into analysis of future emissions scenario and design of air quality and climate change mitigation policies.

  20. Assessment of long-term WRF-CMAQ simulations for understanding direct aerosol effects on radiation "brightening" in the United States

    NASA Astrophysics Data System (ADS)

    Gan, C.-M.; Pleim, J.; Mathur, R.; Hogrefe, C.; Long, C. N.; Xing, J.; Wong, D.; Gilliam, R.; Wei, C.

    2015-11-01

    aerosol semi-direct and/or indirect effects which cannot be readily isolated from the observed data.

  1. Assessment of long-term WRF–CMAQ simulations for understanding direct aerosol effects on radiation "brightening" in the United States

    DOE PAGES

    Gan, C.-M.; Pleim, J.; Mathur, R.; ...

    2015-11-03

    methodology, and aerosol semi-direct and/or indirect effects which cannot be readily isolated from the observed data.« less

  2. Assessment of multi-decadal WRF-CMAQ simulations for understanding direct aerosol effects on radiation "brightening" in the United States

    DOE PAGES

    Gan, C.-M.; Pleim, J.; Mathur, R.; ...

    2015-07-01

    Multi-decadal simulations with the coupled WRF-CMAQ model have been conducted to systematically investigate the changes in anthropogenic emissions of SO2 and NOx over the past 21 years (1990–2010) across the United States (US), their impacts on anthropogenic aerosol loading over North America, and subsequent impacts on regional radiation budgets. In particular, this study attempts to determine the consequences of the changes in tropospheric aerosol burden arising from substantial reductions in emissions of SO2 and NOx associated with control measures under the Clean Air Act (CAA) especially on trends in solar radiation. Extensive analyses conducted by Gan et al. (2014) utilizingmore » observations (e.g. SURFRAD, CASTNET, IMPROVE and ARM) over the past 16 years (1995–2010) indicate a shortwave (SW) radiation (both all-sky and clear-sky) "brightening" in the US. The relationship of the radiation brightening trend with decreases in the aerosol burden is less apparent in the western US. One of the main reasons for this is that the emission controls under the CAA were aimed primarily at reducing pollutants in areas violating national air quality standards, most of which were located in the eastern US while the relatively less populated areas in the western US were less polluted at the beginning of this study period. Comparisons of model results with observations of aerosol optical depth (AOD), aerosol concentration, and radiation demonstrate that the coupled WRF-CMAQ model is capable of replicating the trends well even through it tends to underestimate the AOD. In particular, the sulfate concentration predictions were well matched with the observations. The discrenpancies found in the clear-sky diffuse SW radiation are likely due to several factors such as potential increase of ice particles associated with increasing air traffic, the definition of "clear-sky" in the radiation retrieval methodology and aerosol semi-direct and/or indirect effects which cannot be

  3. Sensitivity of clear-sky direct radiative effect of the aerosol to micro-physical properties by using 6SV radiative transfer model: preliminary results

    NASA Astrophysics Data System (ADS)

    Bassani, Cristiana; Tirelli, Cecilia; Manzo, Ciro; Pietrodangelo, Adriana; Curci, Gabriele

    2015-04-01

    The aerosol micro-physical properties are crucial to analyze their radiative impact on the Earth's radiation budget [IPCC, 2007]. The 6SV model, last generation of the Second Simulation of a Satellite Signal in the Solar Spectrum (6S) radiative transfer code [Kotchenova et al., 2007; Vermote et al., 1997] has been used to perform physically-based atmospheric correction of hyperspectral airborne and aircraft remote sensing data [Vermote et al., 2009; Bassani et al. 2010; Tirelli et al., 2014]. The atmospheric correction of hyperspectral data has been shown to be sensitive to the aerosol micro-physical properties, as reported in Bassani et al., 2012. The role of the aerosol micro-physical properties on the accuracy of the atmospheric correction of hyperspectral data acquired over water and land targets is investigated within the framework of CLAM-PHYM (Coasts and Lake Assessment and Monitoring by PRISMA HYperspectral Mission) and PRIMES (Synergistic use of PRISMA products with high resolution meteo-chemical simulations and their validation on ground and from satellite) projects, both funded by Italian Space Agency (ASI). In this work, the results of the radiative field of the Earth/Atmosphere coupled system simulated by using 6SV during the atmospheric correction of hyperspectral data are presented. The analysis of the clear-sky direct radiative effect is performed considering the aerosol micro-physical properties used to define the aerosol model during the atmospheric correction process. In particular, the AERONET [Holben et al., 1998] and FLEXAOD [Curci et al., 2014] micro-physical properties are used for each image to evaluate the contribution of the size distribution and refractive index of the aerosol type on the surface reflectance and on the direct radiative forcing. The results highlight the potential of the hyperspectral remote sensing data for atmospheric studies as well as for environmental studies. Currently, the future hyperspectral missions, such as the

  4. Aerosol feed direct methanol fuel cell

    NASA Technical Reports Server (NTRS)

    Kindler, Andrew (Inventor); Narayanan, Sekharipuram R. (Inventor); Valdez, Thomas I. (Inventor)

    2002-01-01

    Improvements to fuel cells include introduction of the fuel as an aerosol of liquid fuel droplets suspended in a gas. The particle size of the liquid fuel droplets may be controlled for optimal fuel cell performance by selection of different aerosol generators or by separating droplets based upon size using a particle size conditioner.

  5. Photoacoustics of single laser-trapped nanodroplets for the direct observation of nanofocusing in aerosol photokinetics

    PubMed Central

    Cremer, Johannes W.; Thaler, Klemens M.; Haisch, Christoph; Signorell, Ruth

    2016-01-01

    Photochemistry taking place in atmospheric aerosol droplets has a significant impact on the Earth's climate. Nanofocusing of electromagnetic radiation inside aerosols plays a crucial role in their absorption behaviour, since the radiation flux inside the droplet strongly affects the activation rate of photochemically active species. However, size-dependent nanofocusing effects in the photokinetics of small aerosols have escaped direct observation due to the inability to measure absorption signatures from single droplets. Here we show that photoacoustic measurements on optically trapped single nanodroplets provide a direct, broadly applicable method to measure absorption with attolitre sensitivity. We demonstrate for a model aerosol that the photolysis is accelerated by an order of magnitude in the sub-micron to micron size range, compared with larger droplets. The versatility of our technique promises broad applicability to absorption studies of aerosol particles, such as atmospheric aerosols where quantitative photokinetic data are critical for climate predictions. PMID:26979973

  6. Can a coupled meteorology–chemistry model reproduce the historical trend in aerosol direct radiative effects over the Northern Hemisphere?

    EPA Science Inventory

    The ability of a coupled meteorology–chemistry model, i.e., Weather Research and Forecast and Community Multiscale Air Quality (WRF-CMAQ), to reproduce the historical trend in aerosol optical depth (AOD) and clear-sky shortwave radiation (SWR) over the Northern Hemisphere h...

  7. Jet and ultrasonic nebuliser output: use of a new method for direct measurement of aerosol output.

    PubMed Central

    Dennis, J H; Stenton, S C; Beach, J R; Avery, A J; Walters, E H; Hendrick, D J

    1990-01-01

    Output from jet nebulisers is calibrated traditionally by weighing them before and after nebulisation, but the assumption that the weight difference is a close measure of aerosol generation could be invalidated by the concomitant process of evaporation. A method has been developed for measuring aerosol output directly by using a solute (fluoride) tracer and aerosol impaction, and this has been compared with the traditional weight loss method for two Wright, six Turbo, and four Micro-Cirrus jet nebulisers and two Microinhaler ultrasonic nebulisers. The weight loss method overestimated true aerosol output for all jet nebulisers. The mean aerosol content, expressed as a percentage of the total weight loss, varied from as little as 15% for the Wright jet nebulisers to 54% (range 45-61%) for the Turbo and Micro-Cirrus jet nebulisers under the operating conditions used. In contrast, there was no discrepancy between weight loss and aerosol output for the ultrasonic nebulisers. These findings, along with evidence of both concentrating and cooling effects from jet nebulisation, confirm that total output from jet nebulisers contains two distinct fractions, vapour and aerosol. The vapour fraction, but not the aerosol fraction, was greatly influenced by reservoir temperature within the nebuliser; so the ratio of aerosol output to total weight loss varied considerably with temperature. It is concluded that weight loss is an inappropriate method of calibrating jet nebuliser aerosol output, and that this should be measured directly. PMID:2247862

  8. 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.

  9. Continental pollution in the Western Mediterranean basin: large variability of the aerosol single scattering albedo and influence on the direct shortwave radiative effect

    NASA Astrophysics Data System (ADS)

    Di Biagio, Claudia; Formenti, Paola; Doppler, Lionel; Gaimoz, Cécile; Grand, Noel; Ancellet, Gerard; Attié, Jean-Luc; Bucci, Silvia; Dubuisson, Philippe; Fierli, Federico; Mallet, Marc; Ravetta, François

    2016-08-01

    Pollution aerosols strongly influence the composition of the Western Mediterranean basin, but at present little is known on their optical properties. We report in this study in situ observations of the single scattering albedo (ω) of pollution aerosol plumes measured over the Western Mediterranean basin during the TRAQA (TRansport and Air QuAlity) airborne campaign in summer 2012. Cases of pollution export from different source regions around the basin and at different altitudes between ˜ 160 and 3500 m above sea level were sampled during the flights. Data from this study show a large variability of ω, with values between 0.84-0.98 at 370 nm and 0.70-0.99 at 950 nm. The single scattering albedo generally decreases with the wavelength, with some exception associated to the mixing of pollution with sea spray or dust particles over the sea surface. The lowest values of ω (0.84-0.70 between 370 and 950 nm) are measured in correspondence of a fresh plume possibly linked to ship emissions over the basin. The range of variability of ω observed in this study seems to be independent of the source region around the basin, as well as of the altitude and aging time of the plumes. The observed variability of ω reflects in a large variability for the complex refractive index of pollution aerosols, which is estimated to span in the large range 1.41-1.77 and 0.002-0.097 for the real and the imaginary parts, respectively, between 370 and 950 nm. Radiative calculations in clear-sky conditions were performed with the GAME radiative transfer model to test the sensitivity of the aerosol shortwave Direct Radiative Effect (DRE) to the variability of ω as observed in this study. Results from the calculations suggest up to a 50 and 30 % change of the forcing efficiency (FE), i.e. the DRE per unit of optical depth, at the surface (-160/-235 W m-2 τ-1 at 60° solar zenith angle) and at the Top-Of-Atmosphere (-137/-92 W m-2 τ-1) for ω varying between its maximum and minimum value

  10. Effect of Carbonaceous Aerosols on Clouds and Precipitation in Asia

    NASA Astrophysics Data System (ADS)

    v, V.; Wang, H.; Ganguly, D.; Minghuai, W.; Rasch, P. J.

    2010-12-01

    Carbonaceous aerosols enhance scattering and absorption of solar radiation (i.e., direct radiative effect) in the atmosphere and also affect clouds and precipitation through indirect effects, thus heating the atmosphere but reducing the amount of solar radiation that reaches the earth’s surface. These effects through dynamic feedbacks can also have remote impact over regions far away from their emission sources and hence demand special scientific attention. Previous modeling studies have revealed that large amount of anthropogenic carbonaceous aerosols over the Asian region can alter monsoon circulation and precipitation patterns and thereby influence its strength by varying degrees spatially. Most of the studies focused on the direct radiative effect of aerosols and their subsequent effect on monsoon precipitation. We evaluate the changes in clouds and precipitation in Asia due to carbonaceous aerosols using the community atmospheric model (CAM5) which accounts for not only aerosol direct effects, but also aerosol indirect effects on warm, mixed-phase and cirrus clouds. This study focuses on the precipitation efficiency with emphasis on aerosol indirect effects. In addition to carbonaceous aerosol emissions over Asia, the effect of emissions from other regions like North America, North Africa and Europe are also investigated for their influence on precipitation in the Asian region. In addition to the focus on the aerosol effect on monsoon, we also study the seasonality in aerosol induced changes to precipitation efficiency. We present the quantitative estimates of changes in precipitation efficiency related to changes in aerosol loading and compare them with those estimated from satellite observations, and further explore the potential role of aerosol indirect effects to changes in precipitation efficiency.

  11. 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.

  12. New Directions: Emerging Satellite Observations of Above-cloud Aerosols and Direct Radiative Forcing

    NASA Technical Reports Server (NTRS)

    Yu, Hongbin; Zhang, Zhibo

    2013-01-01

    Spaceborne lidar and passive sensors with multi-wavelength and polarization capabilities onboard the A-Train provide unprecedented opportunities of observing above-cloud aerosols and direct radiative forcing. Significant progress has been made in recent years in exploring these new aerosol remote sensing capabilities and generating unique datasets. The emerging observations will advance the understanding of aerosol climate forcing.

  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. Direct photolysis of α-pinene ozonolysis secondary organic aerosol: effect on particle mass and peroxide content.

    PubMed

    Epstein, Scott A; Blair, Sandra L; Nizkorodov, Sergey A

    2014-10-07

    Primary and secondary organic aerosols (POA and SOA) contain a complex mixture of multifunctional chemicals, many of which are photolabile. Much of the previous work that aimed to understand the chemical evolution (aging) of POA and SOA has focused on the reactive uptake of gas-phase oxidants by particles. By stripping volatile compounds and ozone from α-pinene ozonolysis SOA with three 1-m-long denuders, and exposing the residual particles in a flow cell to near-ultraviolet (λ>300 nm) radiation, we find that condensed-phase photochemistry can induce significant changes in SOA particle size and chemical composition. The particle-bound organic peroxides, which are highly abundant in α-pinene ozonolysis SOA (22 ± 5% by weight), have an atmospheric photolysis lifetime of about 6 days at a 24-h average solar zenith angle (SZA) of 65° experienced at 34° latitude (Los Angeles) in the summer. In addition, the particle diameter shrinks 0.56% per day under these irradiation conditions as a result of the loss of volatile photolysis products. Experiments with and without the denuders show similar results, suggesting that condensed-phase processes dominate over heterogeneous reactions of particles with organic vapors, excess ozone, and gas-phase free radicals. These condensed-phase photochemical processes occur on atmospherically relevant time scales and should be considered when modeling the evolution of organic aerosol in the atmosphere.

  15. How Well Will MODIS Measure Top of Atmosphere Aerosol Direct Radiative Forcing?

    NASA Technical Reports Server (NTRS)

    Remer, Lorraine A.; Kaufman, Yoram J.; Levin, Zev; Ghan, Stephen; Einaudi, Franco (Technical Monitor)

    2000-01-01

    The new generation of satellite sensors such as the Moderate Resolution Imaging Spectroradiometer (MODIS) will be able to detect and characterize global aerosols with an unprecedented accuracy. The question remains whether this accuracy will be sufficient to narrow the uncertainties in our estimates of aerosol radiative forcing at the top of the atmosphere. Satellite remote sensing detects aerosol optical thickness with the least amount of relative error when aerosol loading is high. Satellites are less effective when aerosol loading is low. We use the monthly mean results of two global aerosol transport models to simulate the spatial distribution of smoke aerosol in the Southern Hemisphere during the tropical biomass burning season. This spatial distribution allows us to determine that 87-94% of the smoke aerosol forcing at the top of the atmosphere occurs in grid squares with sufficient signal to noise ratio to be detectable from space. The uncertainty of quantifying the smoke aerosol forcing in the Southern Hemisphere depends on the uncertainty introduced by errors in estimating the background aerosol, errors resulting from uncertainties in surface properties and errors resulting from uncertainties in assumptions of aerosol properties. These three errors combine to give overall uncertainties of 1.5 to 2.2 Wm-2 (21-56%) in determining the Southern Hemisphere smoke aerosol forcing at the top of the atmosphere. The range of values depend on which estimate of MODIS retrieval uncertainty is used, either the theoretical calculation (upper bound) or the empirical estimate (lower bound). Strategies that use the satellite data to derive flux directly or use the data in conjunction with ground-based remote sensing and aerosol transport models can reduce these uncertainties.

  16. 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.

  17. 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.

  18. Anthropogenic Aerosol Effects on Sea Surface Temperatures: Mixed-Layer Ocean Experiments with Explicit Aerosol Representation

    NASA Astrophysics Data System (ADS)

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

    2014-05-01

    Anthropogenic aerosols affect the Earth's radiative balance both through direct and indirect effects. These effects can lead to a reduction of the incoming solar radiation at the surface, i.e. dimming, which may lead to a change in sea surface temperatures (SST) or SST pattern. This, in turn, may affect precipitation patterns. The goal of the present work is to achieve an estimate of the equilibrium SST changes under anthropogenic aerosol forcing since industrialisation. We show preliminary results from mixed-layer ocean (MLO) experiments with explicit aerosol representation performed with ECHAM6-HAM. The (fixed) MLO heat flux into the deep ocean was derived from atmosphere only runs with fixed climatological SSTs (1961-1990 average) and present day (year 2000) aerosols and GHG burdens. Some experiments we repeated with an alternative MLO deep ocean heat flux (based on pre-industrial conditions) to test the robustness of our results with regard to this boundary condition. The maximum surface temperature responses towards anthropogenic aerosol and GHG forcing (separately and combined) were derived on a global and regional scale. The same set of experiments was performed with aerosol and GHG forcings representative of different decades over the past one and a half centuries. This allows to assess how SST patterns at equilibrium changed with changing aerosol (and GHG) forcing. Correlating SST responses with the change in downward clear-sky and all-sky shortwave radiation provides a first estimate of the response to anthropogenic aerosols. Our results show a clear contrast in hemispheric surface temperature response, as expected from the inter-hemispheric asymmetry of aerosol forcing The presented work is part of a project aiming at quantifying the effect of anthropogenic aerosol forcing on SSTs and the consequences for global precipitation patterns. Results from this study will serve as a starting point for further experiments involving a dynamic ocean model, which

  19. Science Overview Document Indirect and Semi-Direct Aerosol Campaign (ISDAC) April 2008

    SciTech Connect

    SJ Ghan; B Schmid; JM Hubbe; CJ Flynn; A Laskin; AA Zelenyuk; DJ Czizco; CN Long; G McFarquhar; J Verlinde; J Harrington; JW Strapp; P Liu; A Korolev; A McDonald; M Wolde; A Fridlind; T Garrett; G Mace; G Kok; S Brooks; D Collins; D Lubin; P Lawson; M Dubey; C Mazzoleni; M Shupe; S Xie; DD Turner; Q Min; EJ Mlawer; D Mitchell

    2007-11-01

    The ARM Climate Research Facility’s (ACRF) Aerial Vehicle Program (AVP) will deploy an intensive cloud and aerosol observing system to the ARM North Slope of Alaska (NSA) locale for a five week Indirect and Semi-Direct Aerosol Campaign (ISDAC) during period 29 March through 30 April 2008. The deployment period is within the International Polar Year, thus contributing to and benefiting from the many ancillary observing systems collecting data synergistically. We will deploy the Canadian National Research Council Convair 580 aircraft to measure temperature, humidity, total particle number, aerosol size distribution, single particle composition, concentrations of cloud condensation nuclei and ice nuclei, optical scattering and absorption, updraft velocity, cloud liquid water and ice contents, cloud droplet and crystal size distributions, cloud particle shape, and cloud extinction. In addition to these aircraft measurements, ISDAC will deploy two instruments at the ARM site in Barrow: a spectroradiometer to retrieve cloud optical depth and effective radius, and a tandem differential mobility analyzer to measure the aerosol size distribution and hygroscopicity. By using many of the same instruments used during Mixed-Phase Arctic Cloud Experiment (M-PACE), conducted in October 2004, we will be able to contrast the arctic aerosol and cloud properties during the fall and spring transitions. The aerosol measurements can be used in cloud models driven by objectively analyzed boundary conditions to test whether the cloud models can simulate the aerosol influence on the clouds. The influence of aerosol and boundary conditions on the simulated clouds can be separated by running the cloud models with all four combinations of M-PACE and ISDAC aerosol and boundary conditions: M-PACE aerosol and boundary conditions, M-PACE aerosol and ISDAC boundary conditions, ISDAC aerosol and M-PACE boundary conditions, and ISDAC aerosol and boundary conditions. ISDAC and M-PACE boundary

  20. Evaluation of Aerosol Direct Radiative Forcing in MIRAGE

    SciTech Connect

    Ghan, Steven J.; Laulainen, Nels S.; Easter, Richard C.; Wagener, Richard; Nemesure, Seth; Chapman, Elaine G.; Zhang, Yang; Leung, Lai-Yung R.

    2001-04-01

    A variety of measurements have been used to evaluate the treatment of aerosol radiative properties and radiative impacts of aerosols simulated by the Model for Integrated Research on Atmospheric Global Exchanges (MIRAGE). The treatment of water uptake in MIRAGE agrees with laboratory measurements for the aerosol components that have been measured. The simulated frequency of relative humidity near 100% is about twice that of European Center for Medium-range Weather Forecasts analyzed relative humidity. When the analyzed relative humidity is used to calculate aerosol water uptake in MIRAGE, the simulated aerosol optical depth agrees with most surface measurements after cloudy conditions are filtered out and differences between model and station elevations are accounted for. Simulated optical depths are low over sites in Brazil during the biomass burning season and over sites in central Canada during the wildfire season, which can be attributed to limitations in the organic and black car bon emissions data used by MIRAGE. The simulated aerosol optical depths are mostly within a factor of two of satellite estimates, but MIRAGE simulates excessively high aerosol optical depths off the east coast of the US and China, and too little dust off the coast of West Africa and in the Arabian Sea. The simulated distribution of single-scatter albedo is consistent with the available in situ surface measurements. The simulated sensitivity of radiative forcing to aerosol optical depth is consistent with estimates from measurements where available. The simulated spatial distribution of aerosol radiance is broadly consistent with estimates from satellite measurements, but with the same errors as the aerosol optical depth. The simulated direct forcing is within the uncertainty of estimates from measurements in the North Atlantic.

  1. 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.

  2. 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.

  3. A direct method for e-cigarette aerosol sample collection.

    PubMed

    Olmedo, Pablo; Navas-Acien, Ana; Hess, Catherine; Jarmul, Stephanie; Rule, Ana

    2016-08-01

    E-cigarette use is increasing in populations around the world. Recent evidence has shown that the aerosol produced by e-cigarettes can contain a variety of toxicants. Published studies characterizing toxicants in e-cigarette aerosol have relied on filters, impingers or sorbent tubes, which are methods that require diluting or extracting the sample in a solution during collection. We have developed a collection system that directly condenses e-cigarette aerosol samples for chemical and toxicological analyses. The collection system consists of several cut pipette tips connected with short pieces of tubing. The pipette tip-based collection system can be connected to a peristaltic pump, a vacuum pump, or directly to an e-cigarette user for the e-cigarette aerosol to flow through the system. The pipette tip-based system condenses the aerosol produced by the e-cigarette and collects a liquid sample that is ready for analysis without the need of intermediate extraction solutions. We tested a total of 20 e-cigarettes from 5 different brands commercially available in Maryland. The pipette tip-based collection system condensed between 0.23 and 0.53mL of post-vaped e-liquid after 150 puffs. The proposed method is highly adaptable, can be used during field work and in experimental settings, and allows collecting aerosol samples from a wide variety of e-cigarette devices, yielding a condensate of the likely exact substance that is being delivered to the lungs.

  4. Simulation of aerosol direct radiative forcing with RAMS-CMAQ in East Asia

    NASA Astrophysics Data System (ADS)

    Zhang, M.; Han, X.; Liu, X.

    2011-12-01

    The air quality modeling system RAMS-CMAQ is developed to assess aerosol direct radiative forcing by linking simulated meteorological parameters and aerosol mass concentration with the aerosol optical properties/radiative transfer module in this study. The module is capable of accounting for important factors that affect aerosol optical properties and radiative effect, such as incident wave length, aerosol size distribution, water uptake, and internal mixture. Subsequently, the modeling system is applied to simulate the temporal and spatial variations in mass burden, optical properties, and direct radiative forcing of diverse aerosols, including sulfate, nitrate, ammonium, black carbon, organic carbon, dust, and sea salt over East Asia throughout 2005. Model performance is fully evaluated using various observational data, including satellite monitoring of MODIS and surface measurements of EANET (Acid Deposition Monitoring Network), AERONET (Aerosol Robotic Network), and CSHNET (Chinese Sun Hazemeter Network). The correlation coefficients of the comparisons of daily average mass concentrations of sulfate, PM2.5, and PM10 between simulations and EANET measurements are 0.70, 0.61, and 0.64, respectively. It is also determined that the modeled aerosol optical depth (AOD) is in congruence with the observed results from the AERONET, the CSHNET, and the MODIS. The model results suggest that the high AOD values ranging from 0.8 to 1.2 are mainly distributed over the Sichuan Basin as well as over central and southeastern China, in East Asia. The aerosol direct radiative forcing patterns generally followed the AOD patterns. The strongest forcing effect ranging from -12 to -8 W/m2 was mainly distributed over the Sichuan Basin and the eastern China's coastal regions in the all-sky case at TOA, and the forcing effect ranging from -8 to -4 W/m2 could be found over entire eastern China, Korea, Japan, East China Sea, and the sea areas of Japan.

  5. Simulation of aerosol direct radiative forcing with RAMS-CMAQ in East Asia

    NASA Astrophysics Data System (ADS)

    Han, Xiao; Zhang, Meigen; Han, Zhiwei; Xin, Jinyuan; Liu, Xiaohong

    2011-11-01

    The air quality modeling system RAMS-CMAQ is developed to assess aerosol direct radiative forcing by linking simulated meteorological parameters and aerosol mass concentration with the aerosol optical properties/radiative transfer module in this study. The module is capable of accounting for important factors that affect aerosol optical properties and radiative effect, such as incident wave length, aerosol size distribution, water uptake, and internal mixture. Subsequently, the modeling system is applied to simulate the temporal and spatial variations in mass burden, optical properties, and direct radiative forcing of diverse aerosols, including sulfate, nitrate, ammonium, black carbon, organic carbon, dust, and sea salt over East Asia throughout 2005. Model performance is fully evaluated using various observational data, including satellite monitoring of MODIS and surface measurements of EANET (Acid Deposition Monitoring Network), AERONET (Aerosol Robotic Network), and CSHNET (Chinese Sun Hazemeter Network). The correlation coefficients of the comparisons of daily average mass concentrations of sulfate, PM2.5, and PM10 between simulations and EANET measurements are 0.70, 0.61, and 0.64, respectively. It is also determined that the modeled aerosol optical depth (AOD) is in congruence with the observed results from the AERONET, the CSHNET, and the MODIS. The model results suggest that the high AOD values ranging from 0.8 to 1.2 are mainly distributed over the Sichuan Basin as well as over central and southeastern China, in East Asia. The aerosol direct radiative forcing patterns generally followed the AOD patterns. The strongest forcing effect ranging from -12 to -8 W m -2 was mainly distributed over the Sichuan Basin and the eastern China's coastal regions in the all-sky case at TOA, and the forcing effect ranging from -8 to -4 W m -2 could be found over entire eastern China, Korea, Japan, East China Sea, and the sea areas of Japan

  6. 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

  7. Global all-sky shortwave direct radiative forcing of anthropogenic aerosols from combined satellite observations and GOCART simulations

    NASA Astrophysics Data System (ADS)

    Su, Wenying; Loeb, Norman G.; Schuster, Gregory L.; Chin, Mian; Rose, Fred G.

    2013-01-01

    Estimation of aerosol direct radiative forcing (DRF) from satellite measurements is challenging because current satellite sensors do not have the capability of discriminating between anthropogenic and natural aerosols. We combine 3-hourly cloud properties from satellite retrievals with two aerosol data sets to calculate the all-sky aerosol direct radiative effect (DRE), which is the mean radiative perturbation due to the presence of both natural and anthropogenic aerosols. The first aerosol data set is based upon Moderate Resolution Imaging Spectroradiometer (MODIS) and Model for Atmospheric Transport and Chemistry (MATCH) assimilation model and is largely constrained by MODIS aerosol optical depth, but it does not distinguish between anthropogenic and natural aerosols. The other aerosol data set is based upon the Goddard Chemistry Aerosol Radiation and Transport (GOCART) model, which does not assimilate aerosol observations but predicts the anthropogenic and natural components of aerosols. Thus, we can calculate the aerosol DRF using GOCART classifications of anthropogenic and natural aerosols and the ratio of DRF to DRE. We then apply this ratio to DRE calculated using MODIS/MATCH aerosols to partition it into DRF (MODIS/MATCH DRF) by assuming that the anthropogenic fractions from GOCART are representative. The global (60°N~60°S) mean all-sky MODIS/MATCH DRF is -0.51 Wm-2 at the top of the atmosphere (TOA), 2.51 Wm-2 within the atmosphere, and -3.02 Wm-2 at the surface. The GOCART all-sky DRF is -0.17 Wm-2 at the TOA, 2.02 Wm-2 within the atmosphere, and -2.19 Wm-2 at the surface. The differences between MODIS/MATCH DRF and GOCART DRF are solely due to the differences in aerosol properties, since both computations use the same cloud properties and surface albedo and the same proportion of anthropogenic contributions to aerosol DRE. Aerosol optical depths simulated by the GOCART model are smaller than those in MODIS/MATCH, and aerosols in the GOCART model are

  8. 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...

  9. Global All-sky Shortwave Direct Radiative Forcing of Anthropogenic Aerosols from Combined Satellite Observations and GOCART Simulations

    NASA Astrophysics Data System (ADS)

    Su, W.; Loeb, N. G.; Schuster, G. L.; Chin, M.; Rose, F. G.

    2013-05-01

    Estimation of aerosol direct radiative forcing (DRF) from satellite measurements is challenging because current satellite sensors do not have the capability of discriminating between anthropogenic and natural aerosols. We combine 3-hourly cloud properties from satellite retrievals with two aerosol data sets to calculate the all-sky aerosol direct radiative effect (DRE), which is the mean radiative perturbation due to the presence of both natural and anthropogenic aerosols. The first aerosol data set is based upon MODIS and MATCH assimilation model and is largely constrained by MODIS aerosol optical depth, but it does not distinguish between anthropogenic and natural aerosols. The other aerosol data set is based upon the GOCART model, which does not assimilate aerosol observations but predicts the anthropogenic and natural components of aerosols. Thus, we can calculate the aerosol DRF using GOCART classifications of anthropogenic and natural aerosols and the ratio of DRF to DRE. We then apply this ratio to DRE calculated using MODIS/MATCH aerosols to partition it into DRF (MODIS/MATCH DRF), by assuming that the anthropogenic fractions from GOCART are representative. The global (60oN ˜60oS) mean all-sky MODIS/MATCH DRF is -0.51 Wm-2 at the TOA, 2.51 Wm-2 within the atmosphere, and -3.02 Wm-2 at the surface. The GOCART all-sky DRF is -0.17 Wm-2 at the TOA, 2.02 Wm-2 within the atmosphere, and -2.19 Wm-2 at the surface. The differences between MODIS/MATCH DRF and GOCART DRF are solely due to the differences in aerosol properties, since both computations use the same cloud properties and surface albedo, and the same proportion of anthropogenic contributions to aerosol DRE. Aerosol optical depths simulated by the GOCART model are smaller than those in MODIS/MATCH, and aerosols in the GOCART model are more absorbing than those in MODIS/MATCH. Large difference in all-sky TOA DRF from these two aerosol data sets highlights the complexity in determining the all-sky DRF

  10. Sensitivity of scattering and absorbing aerosol direct radiative forcing to physical climate factors

    NASA Astrophysics Data System (ADS)

    Ocko, Ilissa B.; Ramaswamy, V.; Ginoux, Paul; Ming, Yi; Horowitz, Larry W.

    2012-10-01

    The direct radiative forcing of the climate system includes effects due to scattering and absorbing aerosols. This study explores how important physical climate characteristics contribute to the magnitudes of the direct radiative forcings (DRF) from anthropogenic sulfate, black carbon, and organic carbon. For this purpose, we employ the GFDL CM2.1 global climate model, which has reasonable aerosol concentrations and reconstruction of twentieth-century climate change. Sulfate and carbonaceous aerosols constitute the most important anthropogenic aerosol perturbations to the climate system and provide striking contrasts between primarily scattering (sulfate and organic carbon) and primarily absorbing (black carbon) species. The quantitative roles of cloud coverage, surface albedo, and relative humidity in governing the sign and magnitude of all-sky top-of-atmosphere (TOA) forcings are examined. Clouds reduce the global mean sulfate TOA DRF by almost 50%, reduce the global mean organic carbon TOA DRF by more than 30%, and increase the global mean black carbon TOA DRF by almost 80%. Sulfate forcing is increased by over 50% as a result of hygroscopic growth, while high-albedo surfaces are found to have only a minor (less than 10%) impact on all global mean forcings. Although the radiative forcing magnitudes are subject to uncertainties in the state of mixing of the aerosol species, it is clear that fundamental physical climate characteristics play a large role in governing aerosol direct radiative forcing magnitudes.

  11. Sensitivity analysis of aerosol direct radiative forcing in ultraviolet visible wavelengths and consequences for the heat budget

    NASA Astrophysics Data System (ADS)

    Hatzianastassiou, N.; Katsoulis, B.; Vardavas, I.

    2004-09-01

    A series of sensitivity studies were performed with a spectral radiative transfer model using aerosol data from the Global Aerosol Data Set (GADS, data available at aerosol/aerosol.htm">http://www.meteo.physik.uni-muenchen.de/strahlung/aerosol/aerosol.htm) in order to investigate and quantify the relative role of key climatic parameters on clear-sky ultraviolet visible direct aerosol radiative forcing at the top of the atmosphere (TOA), within the atmosphere and at the Earth's surface. The model results show that relative humidity and aerosol single-scattering albedo are the most important climatic parameters that determine aerosol forcing at the TOA and at the Earth's surface and atmosphere, respectively. Relative humidity exerts a non-linear positive radiative effect, i.e. increasing humidity amplifies the magnitude of the forcing in the atmosphere and at the surface. Our model sensitivity studies show that increasing relative humidity by 10%, in relative terms, increases the aerosol forcing by factors of 1.42 at the TOA, 1.02 in the atmosphere and 1.17 at the surface. An increase in aerosol single-scattering albedo by 10%, in relative terms, increased the aerosol forcing at the TOA by 1.29, while it decreased the forcing in the atmosphere and at the surface by factors of 0.2 and 0.69, respectively. Our results show that an increase in relative humidity enhances the planetary cooling effect of aerosols (increased reflection of solar radiation to space) over oceans and low-albedo land areas, whilst over polar regions and highly reflecting land surfaces the warming effect of aerosols changes to a cooling effect. Thus, global warming and an associated increase in relative humidity would lead to enhanced aerosol cooling worldwide. The sensitivity results also demonstrate that an increase in surface albedo due to

  12. Effect of aerosol subgrid variability on aerosol optical depth and cloud condensation nuclei: implications for global aerosol modelling

    NASA Astrophysics Data System (ADS)

    Weigum, Natalie; Schutgens, Nick; Stier, Philip

    2016-11-01

    A fundamental limitation of grid-based models is their inability to resolve variability on scales smaller than a grid box. Past research has shown that significant aerosol variability exists on scales smaller than these grid boxes, which can lead to discrepancies in simulated aerosol climate effects between high- and low-resolution models. This study investigates the impact of neglecting subgrid variability in present-day global microphysical aerosol models on aerosol optical depth (AOD) and cloud condensation nuclei (CCN). We introduce a novel technique to isolate the effect of aerosol variability from other sources of model variability by varying the resolution of aerosol and trace gas fields while maintaining a constant resolution in the rest of the model. We compare WRF-Chem (Weather and Research Forecast model) runs in which aerosol and gases are simulated at 80 km and again at 10 km resolutions; in both simulations the other model components, such as meteorology and dynamics, are kept at the 10 km baseline resolution. We find that AOD is underestimated by 13 % and CCN is overestimated by 27 % when aerosol and gases are simulated at 80 km resolution compared to 10 km. The processes most affected by neglecting aerosol subgrid variability are gas-phase chemistry and aerosol uptake of water through aerosol-gas equilibrium reactions. The inherent non-linearities in these processes result in large changes in aerosol properties when aerosol and gaseous species are artificially mixed over large spatial scales. These changes in aerosol and gas concentrations are exaggerated by convective transport, which transports these altered concentrations to altitudes where their effect is more pronounced. These results demonstrate that aerosol variability can have a large impact on simulating aerosol climate effects, even when meteorology and dynamics are held constant. Future aerosol model development should focus on accounting for the effect of subgrid variability on these

  13. Direct radiative forcing of aerosols in cloudy condition using CALIPSO satellite data

    NASA Astrophysics Data System (ADS)

    Oikawa, E.; Nakajima, T.; Winker, D. M.

    2013-12-01

    The aerosol direct effect occurs by direct scattering and absorption of solar and thermal radiation. Shortwave direct aerosol radiative forcing (DARF) under clear-sky condition is estimated about 5 Wm-2 from satellite retrievals and model simulations [Yu et al., 2006ACP]. Simultaneous observations of aerosols and clouds are very limited, thus it is difficult to validate the estimation of DARF under cloudy-sky condition. In 2006, the CALIPSO (Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observations) satellite was launched with the space-borne lidar, CALIOP (Cloud-Aerosol Lidar with Orthogonal Polarization). This enabled us to get data of the vertical distribution of aerosols and clouds all over the world. Oikawa et al. [2013JGR] estimated DARF under clear-sky, cloudy-sky, and all-sky conditions using CALIPSO and MODIS (Moderate resolution Imaging Spectrometer) data. Over Atlantic Ocean off southwest Africa, biomass burning aerosols are transported above low-level clouds and cause large positive DARF [Oikawa et al., 2013JGR; Chand et al., 2009Nat. Geosci.; De Graaf et al., 2012JGR; Takemura et al., 2005JGR]. We calculate DARF using CALIOP Level 2 Cloud and Aerosol Layer Products Version 3 and the method of Oikawa et al. [2013]. In this study, we focus on the case that aerosols exist above clouds (above-cloud case) in 2007. Over Atlantic Ocean off southwest Africa, DARF caused by smoke aerosols is +7.1 Wm-2 in September. On the other hand, aerosol optical thickness (AOT) of smoke is small as close to 0 Wm-2 in spring season. Over North Pacific, yellow sand and industrial smoke are transported from Asia and DARF is +5.2 Wm-2 in May. Dust AOT at 532 nm is 0.014 and polluted dust AOT at 532 nm is 0.052; in other words, a large part of dust emitted from Taklamakan and Gobi deserts are mixed with the industrial smoke and transported to the Pacific Ocean according to the CALIPSO algorithms.

  14. 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

  15. Direct radiative forcing from black carbon aerosols over urban environment

    NASA Astrophysics Data System (ADS)

    Badarinath, K. V. S.; Madhavi Latha, K.

    There is growing evidence that the earth’s climate is changing and will likely continue to change in the future. It is still debated whether these changes are due to natural variability of the climate system or a result of increases in the concentration of greenhouse gases in the atmosphere. Black carbon (BC) has become the subject of interest for a variety of reasons. BC aerosol may cause environmental as well as harmful health effects in densely inhabited regions. BC is a strong absorber of radiation in the visible and near-infrared part of the spectrum, where most of the solar energy is distributed. Black carbon is emitted into the atmosphere as a byproduct of all combustion processes, viz., vegetation burning, industrial effluents and motor vehicle exhausts, etc. In this paper, we present results from our measurements on black carbon aerosols, total aerosol mass concentration and aerosol optical depth over an urban environment namely Hyderabad during January to May, 2003. Diurnal variations of BC indicate high BC concentrations during 6:00 9:00 and 19:00 23:00 h. Weekday variations of BC concentrations increase gradually from Monday to Wednesday and gradually decrease from Thursday to Sunday. Analysis of traffic density along with meteorological parameters suggests that the primary determinant for BC concentration levels and patterns is traffic density. Seasonal variations of BC suggest that the BC concentrations are high during dry season compared to rainy season due to the scavenging by air. The fraction of BC to total mass concentration has been observed to be 7% during January to May. BC showed positive correlation with total mass concentration and aerosol optical depth at 500 nm. Radiative transfer calculations suggests that during January to May, diurnal averaged aerosol forcing at the surface is -33 Wm2 and at the top of the atmosphere (TOA) above 100 km it is observed to be +9 Wm-2. The results have been discussed in detail in the paper.

  16. The impact of aerosol optical depth assimilation on aerosol forecasts and radiative effects during a wild fire event over the United States

    NASA Astrophysics Data System (ADS)

    Chen, D.; Liu, Z.; Schwartz, C. S.; Lin, H.-C.; Cetola, J. D.; Gu, Y.; Xue, L.

    2014-11-01

    The Gridpoint Statistical Interpolation three-dimensional variational data assimilation (DA) system coupled with the Weather Research and Forecasting/Chemistry (WRF/Chem) model was utilized to improve aerosol forecasts and study aerosol direct and semi-direct radiative feedbacks during a US wild fire event. Assimilation of MODIS total 550 nm aerosol optical depth (AOD) retrievals clearly improved WRF/Chem forecasts of surface PM2.5 and organic carbon (OC) compared to the corresponding forecasts without aerosol data assimilation. The scattering aerosols in the fire downwind region typically cooled layers both above and below the aerosol layer and suppressed convection and clouds, which led to an average of 2% precipitation decrease during the fire week. This study demonstrated that, even with no input of fire emissions, AOD DA improved the aerosol forecasts and allowed a more realistic model simulation of aerosol radiative effects.

  17. The impact of aerosol optical depth assimilation on aerosol forecasts and radiative effects during a wild fire event over the United States

    NASA Astrophysics Data System (ADS)

    Chen, D.; Liu, Z.; Schwartz, C. S.; Lin, H.-C.; Cetola, J. D.; Gu, Y.; Xue, L.

    2014-06-01

    The Gridpoint Statistical Interpolation three-dimensional variational data assimilation (DA) system coupled with the Weather Research and Forecasting/Chemistry (WRF/Chem) model was utilized to improve aerosol forecasts and study aerosol direct and semi-direct radiative feedbacks during a US wild fire event. Assimilation of MODIS total 550 nm aerosol optical depth (AOD) retrievals clearly improved WRF/Chem forecasts of surface PM2.5 and organic carbon (OC) compared to the corresponding forecasts without aerosol data assimilation. The scattering aerosols in the fire downwind region typically cooled layers both above and below the aerosol layer and suppressed convection and clouds, which led to an average 2% precipitation decease during the fire week. This study demonstrated that even with no input of fire emissions, AOD DA improved the aerosol forecasts and allowed a more realistic model simulation of aerosol radiative effects.

  18. Climate Response to Warm Cloud-Aerosol Interactions: Comparisons With Direct Aerosol and Long-Lived Greenhouse Gas Impacts

    NASA Astrophysics Data System (ADS)

    Ramaswamy, V.; Ming, Y.

    2006-12-01

    We employ the NOAA/ GFDL global atmospheric model coupled to a mixed-layer ocean to investigate the mechanisms and quantitative aspects underlying the radiative perturbations and climate response arising due to cloud-aerosol interactions in low-lying clouds. The aerosol species considered include sulfate, sea-salt and carbonaceous species, whose space-time distributions are determined offline by the MOZART 2 chemistry- transport model based on emissions data. The model's prognostic cloud scheme of liquid water and amount is expanded to include cloud droplet concentration in a way that importantly allows them to be computed using the same large-scale and convective updraft velocity field. The equilibrium response of the model's global climate system to the change in aerosols from pre- industrial to present-day is evaluated, in terms of the forcing applied and the role of the large- and cloud-scale feedback mechanisms. The cloud characteristics simulated are compared against observations, while the model's response is compared with that obtained from using a diagnostic aerosol-cloud relationship to highlight the significance of specific cloud microphysical processes. The spatial distributions of the thermal and hydrologic responses are also compared with those resulting from simulations performed for the pre-industrial to present-day direct aerosol effect. The temperature responses in the low and high latitudes, including changes in the large-scale precipitation pattern, are contrasted with those due to the well-mixed greenhouse gases. The forcing-response relationship is examined for the radiative perturbations investigated, with surface radiative forcing included in these considerations. We finally investigate the concept of linear additivity of the responses in various climate variables for the set of radiative perturbations considered above, extending from the global- and zonal-mean to continental scales.

  19. Background on health effects of acid aerosols

    SciTech Connect

    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 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.

  20. Effects of aerosol organics on cloud condensation nucleus (CCN) concentration and first indirect aerosol effect

    SciTech Connect

    Wang, J. X.; Lee, Y.- N.; Daum, Peter H.; Jayne, John T.; Alexander, M. L.

    2008-11-03

    Abstract. Aerosol microphysics, chemical composition, and CCN properties were measured on the Department of Energy Gulfstream-1 aircraft during the Marine Stratus/ Stratocumulus Experiment (MASE) conducted over the coastal waters between Point Reyes National Seashore and Monterey Bay, California, in July 2005. Aerosols measured during MASE included free tropospheric aerosols, marine boundary layer aerosols, and aerosols with high organic concentration within a thin layer above the cloud. Closure analysis was carried out for all three types of aerosols by comparing the measured CCN concentrations at 0.2% supersaturation to those predicted based on size distribution and chemical composition using K¨ohler theory. The effect of aerosol organic species on predicted CCN concentration was examined using a single hygroscopicity parameterization.

  1. 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.

  2. Direct gravimetric determination of aerosol mass concentration in central antarctica.

    PubMed

    Annibaldi, Anna; Truzzi, Cristina; Illuminati, Silvia; Scarponi, Giuseppe

    2011-01-01

    In Antarctica, experimental difficulties due to extreme conditions have meant that aerosol mass has rarely been measured directly by gravimetry, and only in coastal areas where concentrations were in the range of 1-7 μg m(-3). The present work reports on a careful differential weighing methodology carried out for the first time on the plateau of central Antarctica (Dome C, East Antarctica). To solve problems of accurate aerosol mass measurements, a climatic room was used for conditioning and weighing filters. Measurements were carried out in long stages of several hours of readings with automatic recording of temperature/humidity and mass. This experimental scheme allowed us to sample from all the measurements (up to 2000) carried out before and after exposure, those which were recorded under the most stable humidity conditions and, even more importantly, as close to each other as possible. The automatic reading of the mass allowed us in any case to obtain hundreds of measurements from which to calculate average values with uncertainties sufficiently low to meet the requirements of the differential weighing procedure (±0.2 mg in filter weighing, between ±7% and ±16% both in aerosol mass and concentration measurements). The results show that the average summer aerosol mass concentration (aerodynamic size ≤10 μm) in central Antarctica is about 0.1 μg m(-3), i.e., about 1/10 of that of coastal Antarctic areas. The concentration increases by about 4-5 times at a site very close to the station.

  3. Direct radiative forcing from black carbon aerosols over urban environment

    NASA Astrophysics Data System (ADS)

    Madhavi Latha, K.; Badarinath, K. V. S.

    There is growing evidence that the earth's climate is changing and will likely continue to change in the future. It is still debated whether these changes are due to natural variability of the climate system or a result of increases in the concentration of greenhouse gases in the atmosphere. Black carbon (BC) has become the subject of interest for a variety of reasons. BC aerosol may cause environmental as well as harmful health effects in densely inhabited regions. BC is a strong absorber of radiation in the visible and near-infrared part of the spectrum, where most of the solar energy is distributed. Black carbon is emitted into the atmosphere as a byproduct of all combustion processes viz., vegetation burning, industrial effluents and motor vehicle exhausts etc. In this paper, we present results from our measurements on black carbon aerosols, total aerosol mass concentration and aerosol optical depth over an urban environment namely Hyderabad during January to May, 2003. Diurnal variations of BC suggests that high BC concentrations observed during 6:00-9:00hrs and 19:00-23:00hrs. Weekday variations of BC suggest that the day average BC concentrations increases gradually from Monday to Wednesday and gradually decreased from Thursday to Sunday. Analysis of traffic density along with meteorological parameters suggests that the primary determinant for BC concentration levels and patterns is traffic density. Seasonal variations of BC suggest that the BC concentrations are high during dry season compared to rainy season due to scavenging effects of BC during rainy season. Fraction of BC to total mass concentration has been observed to be 7% during January to May. BC showed positive correlation with total mass concentration and aerosol optical depth at 500nm. Radiative transfer calculations suggests that during January to May, diurnal averaged aerosol forcing at the surface calculated to be -33Wm -2 and at the top of the atmosphere (TOA) it is observed to +9 Wm -2. The

  4. Direct contact test for estimating the ecotoxicity of aerosol samples.

    PubMed

    Kováts, Nora; Acs, András; Kovács, Anikó; Ferincz, Arpád; Turóczi, Beatrix; Gelencsér, András

    2012-03-01

    Atmospheric particulate matter with aerodynamic diameter less than 10 μm (PM10) and 2.5 μm (PM2.5) is now identified as one of the most dangerous pollutants on human health by the EU new directive on air quality (2008/50/CE). Although these primary pollutants are monitored in cities, little information is available on their ecotoxicity. In this paper a 'whole-aerosol' testing protocol is suggested based on the kinetic version of the Vibrio fischeri bioluminescence inhibition test.

  5. Effect of aerosolization on subsequent bacterial survival.

    PubMed Central

    Walter, M V; Marthi, B; Fieland, V P; Ganio, L M

    1990-01-01

    To determine whether aerosolization could impair bacterial survival, Pseudomonas syringae and Erwinia herbicola were aerosolized in a greenhouse, the aerosol was sampled at various distances from the site of release by using all-glass impingers, and bacterial survival was followed in the impingers for 6 h. Bacterial survival subsequent to aerosolization of P. syringae and E. herbicola was not impaired 1 m from the site of release. P. syringae aerosolized at 3 to 15 m from the site of release at a temperature of 12 degrees C and a relative humidity of 80% survived 35- to 65-fold better than P. syringae released at 27 degrees C and a relative humidity of 40%. No difference was observed in the survival of P. syringae and E. herbicola following aerosolization at the same temperature and relative humidity. Bacteria sprayed directly onto bean and oat plants established stable populations at comparable numbers on both plants over an 8-day period following inoculation. Bacteria that inoculated adjacent plants by drifting downwind up to 5 m were detectable at an initial population of 10(2) CFU/g on oats and 10(5) CFU/g on beans 2 h after the spray. However, bacterial populations on both plants were undetectable within 48 h. PMID:2268157

  6. Assessing the direct occupational and public health impacts of solar radiation management with stratospheric aerosols.

    PubMed

    Effiong, Utibe; Neitzel, Richard L

    2016-01-19

    Geoengineering is the deliberate large-scale manipulation of environmental processes that affects the Earth's climate, in an attempt to counteract the effects of climate change. Injecting sulfate aerosol precursors and designed nanoparticles into the stratosphere to (i.e., solar radiation management [SRM]), has been suggested as one approach to geoengineering. Although much is being done to unravel the scientific and technical challenges around geoengineering, there have been few efforts to characterize the potential human health impacts of geoengineering, particularly with regards to SRM approaches involving stratospheric aerosols. This paper explores this information gap. Using available evidence, we describe the potential direct occupational and public health impacts of exposures to aerosols likely to be used for SRM, including environmental sulfates, black carbon, metallic aluminum, and aluminum oxide aerosols. We speculate on possible health impacts of exposure to one promising SRM material, barium titanate, using knowledge of similar nanomaterials. We also explore current regulatory efforts to minimize exposure to these toxicants. Our analysis suggests that adverse public health impacts may reasonably be expected from SRM via deployment of stratospheric aerosols. Little is known about the toxicity of some likely candidate aerosols, and there is no consensus regarding acceptable levels for public exposure to these materials. There is also little infrastructure in place to evaluate potential public health impacts in the event that stratospheric aerosols are deployed for solar radiation management. We offer several recommendations intended to help characterize the potential occupation and public health impacts of SRM, and suggest that a comprehensive risk assessment effort is needed before this approach to geoengineering receives further consideration.

  7. Linking Aerosol Source Activities to Present and Future Climate Effects

    NASA Astrophysics Data System (ADS)

    Koch, D.; Bond, T. C.; Streets, D.; Menon, S.; Unger, N.

    2007-05-01

    Aerosol source sectors (transport, power, industry, residential, biomass burning) generate distinct mixtures of aerosol species. These mixtures in turn have different effects on climate. As sectoral emissions change in coming decades, whether by regulation or not, it is helpful to link pollution from source types to climate consequences. We do so, using our global (GISS GCM) aerosol model for present and future IPCC SRES scenarios. According to our model, residential and transport sectors have net positive 1995 aerosol forcings (0.04 and 0.03 W m-2) due to their large black carbon contents. However, the sulfate-dominated power and industry sectors have net negative 1995 forcings (-0.10 and -0.09 W m-2). Due to the near-balance of absorbing and scattering components, biomass burning forcing is small. For the 2050 SRES A1B scenario, the net (negative) aerosol forcing is double 1995 due primarily to increased sulfur emissions in the industry and power sectors. For 2050 B1 the net (negative) forcing decreases relative to 1995, as sulfur emissions are reduced. Both future scenarios project decreasing residential emissions. Yet transport emissions are expected to remain significant and thus become the dominant source of warming aerosols in the future. Aerosol pollution is projected to shift southward relative to the present, as the current industrialized regions generally reduce emissions and tropical and southern hemispheric regions continue to develop. Similar to these SRES scenarios, IIASA scenarios project a decline in residential emissions; however IIASA is more optimistic about transport sector emissions reductions. We will conduct present-day climate experiments, including aerosol direct and indirect effects, to study impacts of power and transport sectors on climate features such as air temperature and hydrologic cycle.

  8. Measurements of Semi-volatile Aerosol and Its Effect on Aerosol Optical Properties During Southern Oxidant and Aerosol Study

    NASA Astrophysics Data System (ADS)

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

    2013-12-01

    Semi-volatile compounds, including particle-bound water, comprise a large part of aerosol mass and have a significant influence on aerosol lifecycle and its optical properties. Understanding the properties of semi-volatile compounds, especially those pertaining to gas/aerosol partitioning, is of critical importance for our ability to predict concentrations and properties of ambient aerosol. 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 temperature and relative humidity 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). In parallel to these measurements, a long residence time temperature-stepping thermodenuder and a variable residence time constant temperature thermodenuder in combination with three SMPS systems and an Aerosol Chemical Speciation Monitor (ACSM) were used to assess aerosol volatility and kinetics of aerosol evaporation. It was found that both temperature and relative humidity have a strong effect on aerosol optical properties. The variable residence time thermodenuder data suggest that aerosol equilibrated fairly quickly, within 2 s, in contrast to other ambient observations. Preliminary analysis show that approximately 50% and 90% of total aerosol mass evaporated at temperatures of 100 C and 180C, respectively. Evaporation varied substantially with ambient aerosol loading and composition and meteorology. During course of this study, T50 (temperatures at which 50% aerosol mass evaporates) varied from 60 C to more than 120 C.

  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. Aerosol indirect effect dictated by liquid clouds

    NASA Astrophysics Data System (ADS)

    Christensen, Matthew W.; Chen, Yi-Chun; Stephens, Graeme L.

    2016-12-01

    Anthropogenic aerosols have been shown to enhance the solar reflection from warm liquid clouds and mask part of the warming due to the buildup of greenhouse gases. However, very little is known about the effects of aerosol on mixed-phase stratiform clouds as well as other cloud regimes including cumulus, altocumulus, nimbostratus, deep convection, and anvil cirrus. These additional cloud categories are ubiquitous and typically overlooked in satellite-based assessments of the global aerosol indirect forcing. Here we provide their contribution to the aerosol indirect forcing estimate using satellite data collected from several colocated sensors in the A-train for the period 2006-2010. Cloud type is determined according to the 2B-CLDCLASS-LIDAR CloudSat product, and the observations are matched to the radiative flux measurements from CERES (Clouds and the Earth's Radiant Energy System) and aerosol retrievals from MODIS (MODerate resolution Imaging Spectroradiometer). The oceanic mean aerosol indirect forcing is estimated to be -0.20 ± 0.31 W m-2 with warm low-level cloud largely dictating the strength of the response (-0.36 ± 0.21 W m-2) due to their abundance and strong cloud albedo effect. Contributions from mixed-phase low-level cloud (0.01 ± 0.06 W m-2) and convective cloud (0.15 ± 0.23 W m-2) are positive and buffer the system due to strong aerosol-cloud feedbacks that reduce the cloud albedo effect and/or lead to convective invigoration causing a countering positive longwave warming response. By combining all major cloud categories together, aerosol indirect forcing decreases and now contains positive values in the uncertainty estimate.

  11. Regional simulation of aerosol radiative effects and their influence on rainfall over India using WRFChem model

    NASA Astrophysics Data System (ADS)

    Kedia, Sumita; Cherian, Ribu; Islam, Sahidul; Das, Subrata Kumar; Kaginalkar, Akshara

    2016-12-01

    A regional climate model, WRFChem has been utilized to simulate aerosol and rainfall distribution over India during July 2010 which was a normal monsoon year. Two identical simulations, one includes aerosol feedback via their direct and indirect effects and other one without any aerosol effect, are structured to understand the impact of aerosol net (direct + indirect) effect on rainfall pattern over India. Model results are accompanied by satellite and ground based observations to examine the robustness of the model simulations. It is shown that the model can reproduce the spatial and temporal characteristics of meteorological parameters, rainfall distribution, aerosol optical depth and single scattering albedo reasonably well. Model simulated spatial distribution and magnitude of aerosol optical depth over India are realistic, particularly over northwest India, where mineral dust is a major contributor to the total aerosol loading and over Indo-Gangetic Plain region (IGP) where AOD remains high throughout the year. Net (shortwave + longwave) atmospheric heating rate is the highest (> 0.27 K day - 1) over east IGP due to abundant dust and anthropogenic aerosols while it is the lowest over peninsular India and over the Thar desert (< 0.03 K day - 1) which can be attributed to less aerosol concentration and longwave cooling, respectively. It is shown that, inclusion of aerosol direct and indirect effects have strong influence ( ± 20%) on rainfall magnitude and its distribution over Indian subcontinent during monsoon.

  12. 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

  13. 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

  14. A study of the aerosol radiative properties needed to compute direct aerosol forcing in the southeastern United States

    NASA Astrophysics Data System (ADS)

    Yu, Shaocai; Saxena, V. K.; Wenny, B. N.; Deluisi, J. J.; Yue, G. K.; Petropavlovskikh, I. V.

    2000-10-01

    To assess the direct radiative forcing due to aerosols in southeastern United States where a mild cooling is under way, an accurate set of data describing the aerosol radiative properties are needed. We report here aerosol optical depth (AOD) and diffuse to-direct solar irradiance ratio (DDR) at three operational wavelengths (415, 500, 673 nm) determined by using Multifilter Rotating Shadowband Radiometers (MFRSR) at two sites (a mountain top site: Mount Gibbes, 35.78°N, 82.29°W, 2006 m mean sea level (msl); a valley site: Black Mountain, 35.66°N, 82.38°W, 951 m msl), which are separated horizontally by 10 km and vertically by 1 km. The characteristics AOD and DDR were determined from the field measurements obtained during 1995. It was found that the representative total AOD values at 500 nm at the valley site for highly polluted (HP), marine (M) and continental (C) air masses were 0.68±0.33, 0.29±0.19, and 0.10±0.04, respectively. The fact that the ratio of the mean 1 km layer optical depth to total mean optical depth at 500 nm from the valley site was 71% indicates that the major portion of the atmospheric aerosol was located in the lowest 1 km surface boundary layer (SBL). There was a significant linear correlation between the DDR and the total AOD at both sites. A simple, fast, and operative search-graph method was used to retrieve the columnar size distribution (number concentration N effective radius reff, and geometric standard deviation σg) from the optical depth observations at the three operational wavelengths. The ground albedo, single-scattering albedo, and imaginary part of the refractive index are calculated using a mathematically unique procedure involving a Mie code and a radiative transfer code in conjunction with the retrieved aerosol size distribution, AOD, and DDR. It was found that N, reff, and σg were in the range of 1.9×10 to 1.7×104 cm-3, 0.09-0.68 μm, and 1.12-2.70, respectively. The asymmetry factor and single-scattering albedo

  15. Climatic Effects of Marine Organic Aerosols

    NASA Astrophysics Data System (ADS)

    Xu, J.; Meskhidze, N.; Zhang, Y.; Gantt, B.; Ghan, S. J.; Nenes, A.; Liu, X.; Easter, R. C.; Zaveri, R. A.

    2009-12-01

    Recent studies suggest that the emissions of primary organic matter (POM) of marine biogenic origin and secondary organic aerosol (SOA) from phytoplankton-produced volatile organic compounds can lead to changes of chemical composition and size distribution of marine aerosol, thus modifying the cloud droplet activation potential and affecting climate. In this study, the effects of marine organic aerosol emissions and the dissolved marine organic aerosol components as surfactant are explored using the National Center of Atmospheric Research’s Community Atmosphere Model, coupled with the Pacific Northwest National Laboratory’s Modal Aerosol Model (CAM-MAM). Primary marine organic aerosol emissions are separated into sub- and super-micron modes, and calculated based on wind speed-dependent sea-spray mass flux and remotely-sensed surface chlorophyll-a concentration. Two distinct sea spray emission functions used in this study yield different amounts and spatial distributions of sub-micron marine POM mass flux. The super-micron sea-spray flux is determined based on simulated sea-spray number flux. Both sub and super-micron marine POM are assumed to be mostly water-insoluble and added in the accumulation mode and coarse sea-salt mode, respectively. A prescribed soluble mass fraction of 50% is assumed for marine SOA, formed from phytoplankton-emitted isoprene and allowed to be condensed on existing aerosols in different modes. Surfactant effects from the soluble part of sub-micron marine POM are included in the cloud droplet activation parameterization by some modifications based on the mass fraction of dissolved marine POM. 10 year model simulations are conducted to examine the effects of marine organic aerosols on cloud microphysical and optical properties. Analyses of model results show that different marine aerosol emissions and cloud droplet activation mechanisms can yield 9% to 16% increase in global maritime mean cloud droplet number concentration. Changes

  16. Implementation and initial application of new chemistry-aerosol options in WRF/Chem for simulating secondary organic aerosols and aerosol indirect effects for regional air quality

    NASA Astrophysics Data System (ADS)

    Wang, Kai; Zhang, Yang; Yahya, Khairunnisa; Wu, Shiang-Yuh; Grell, Georg

    2015-08-01

    Atmospheric aerosols play important roles in affecting regional meteorology and air quality through aerosol direct and indirect effects. Two new chemistry-aerosol options have been developed in WRF/Chem v3.4.1 by incorporating the 2005 Carbon Bond (CB05) mechanism and coupling it with the existing aerosol module MADE with SORGAM and VBS modules for simulating secondary organic aerosol (SOA), aqueous-phase chemistry in both large scale and convective clouds, and aerosol feedback processes (hereafter CB05-MADE/SORGAM and CB05-MADE/VBS). As part of the Air Quality Model Evaluation International Initiative (AQMEII) Phase II model intercomparison that focuses on online-coupled meteorology and chemistry models, WRF/Chem with the two new options is applied to an area over North America for July 2006 episode. The simulations with both options can reproduce reasonably well most of the observed meteorological variables, chemical concentrations, and aerosol/cloud properties. Compared to CB05-MADE/SORGAM, CB05-MADE/VBS greatly improves the model performance for organic carbon (OC) and PM2.5, reducing NMBs from -81.2% to -13.1% and from -26.1% to -15.6%, respectively. Sensitivity simulations show that the aerosol indirect effects (including aqueous-phase chemistry) can reduce the net surface solar radiation by up to 53 W m-2 with a domainwide mean of 12 W m-2 through affecting cloud formation and radiation scattering and reflection by increasing cloud cover, which in turn reduce the surface temperature, NO2 photolytic rate, and planetary boundary layer height by up to 0.3 °C, 3.7 min-1, and 64 m, respectively. The changes of those meteorological variables further impact the air quality through the complex chemistry-aerosol-cloud-radiation interactions by reducing O3 mixing ratios by up to 5.0 ppb. The results of this work demonstrate the importance of aerosol indirect effects on the regional climate and air quality. For comparison, the impacts of aerosol direct effects on both

  17. 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.

  18. 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

  19. Long-term AOD timeseries by Precision Filter Radiometer and assessment of radiative forcing due to the aerosol direct effect at four sites in Switzerland over the last two decades.

    NASA Astrophysics Data System (ADS)

    Martucci, Giovanni; Vuilleumier, Laurent

    2016-04-01

    In association with the WMO GAW Precision Filter Radiometer network, MeteoSwiss operates four automatic stations measuring the direct solar irradiance in 16 narrow spectral bands within the range 305-1024 nm since 1998. The four sites are (i) Payerne (timeseries 2002-2016), characterized by rural environment (Swiss plateau), (ii) Davos (timeseries 1998-2016), characterized by alpine environment, (iii) Jungfraujoch (timeseries 1999-2016), characterized by alpine environment and partial free tropospheric conditions (mainly in winter, Hermann et al, 2015), and (iv) Locarno-Monti (timeseries 2001-2016), characterized by semi-alpine and urban environment (southern side of the Swiss-Italian Alps). WE present the long-term, almost uninterrupted, timeseries of Aerosol Optical Depth (AOD) in the spectral range 368-1024 nm that has been calculated for each of the four sites along the last two decades. Additionally, we present a study of the trends over almost twenty years of the AOD at different wavelengths. Based on the simulations of the LibRadtran software package for radiative transfer calculations (Meyer and Kylling, 2005) and on the PFR-based timeseries of AOD it has been possible to assess the radiative forcing due to the direct effect of aerosols over Switzerland since 1998.

  20. Quantifying the climatological cloud-free direct radiative forcing of aerosol over the Red Sea

    NASA Astrophysics Data System (ADS)

    Brindley, Helen; Osipov, Serega; Bantges, Richard; Smirnov, Alexander; Banks, Jamie; Levy, Robert; Prakash, P.-Jish; Stenchikov, Georgiy

    2015-04-01

    A combination of ground-based and satellite observations are used, in conjunction with column radiative transfer modelling, to assess the climatological aerosol loading and quantify its corresponding cloud-free direct radiative forcing (DRF) over the Red Sea. While there have been campaigns designed to probe aerosol-climate interactions over much of the world, relatively little attention has been paid to this region. Because of the remoteness of the area, satellite retrievals provide a crucial tool for assessing aerosol loading over the Sea. However, agreement between aerosol properties inferred from measurements from different instruments, and even in some cases from the same measurements using different retrieval algorithms can be poor, particularly in the case of mineral dust. Ground based measurements which can be used to evaluate retrievals are thus highly desirable. Here we take advantage of ship-based sun-photometer micro-tops observations gathered from a series of cruises which took place across the Red Sea during 2011 and 2013. To our knowledge these data represent the first set of detailed aerosol measurements from the Sea. They thus provide a unique opportunity to assess the performance of satellite retrieval algorithms in this region. Initially two aerosol optical depth (AOD) retrieval algorithms developed for the MODerate Resolution Imaging Spectroradiometer (MODIS) and Spinning Enhanced Visible and InfraRed Imager (SEVIRI) instruments are evaluated via comparison with the co-located cruise observations. These show excellent agreement, with correlations typically better than 0.9 and very small root-mean-square and bias differences. Calculations of radiative fluxes and DRF along one of the cruises using the observed aerosol and meteorological conditions also show good agreement with co-located estimates from the Geostationary Earth Radiation Budget (GERB) instrument if the aerosol asymmetry parameter is adjusted to account for the presence of large

  1. 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.

  2. Assessing effects of esfenvalerate aerosol applications on resident populations of Tribolium castaneum (Herbst), the red flour beetle, through direct and indirect sampling

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Small-scale field sheds were infested with resident populations of the red flour beetle, Tribolium castaneum (Herbst), and either left untreated or treated every two or four weeks with an aerosol spray of esfenvalerate (Conquer ®). The sheds were infested by placing flour food patches underneath she...

  3. 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.

  4. Radiative effects of aerosols on the environment in China

    NASA Astrophysics Data System (ADS)

    Yu, Hongbin

    Anthropogenic emissions and concentrations of aerosol precursors and aerosols over China are among the highest in major countries of the world. Due to large emissions of soot and dust, aerosol absorption is high. Based on the observed direct and diffuse irradiance, a single scattering albedo of about 0.8 is derived for two large agri/eco/industrial areas. Aerosol direct effect can exert various environmental impacts in China. Photochemical activities in the atmospheric boundary layer (ABL) are significantly reduced because of reductions in photolysis rates and in emissions of biogenic hydrocarbons. Crop yields under optimal conditions can be reduced due to the reduction in surface solar irradiance. The most significant aerosol radiative perturbation is in changing the air-surface interaction and diurnal evolution of ABL. Reductions in various surface heat fluxes due to aerosols depend on soil moisture. Over a relatively dry surface, the evaporation has a small change, leading to the largest decrease of surface skin temperature at noon. Over a relatively wet surface, a substantial reduction in evaporation results in the largest surface cooling in the early morning. The diurnal temperature range (DTR) can be reduced by an amount comparable to the observed decrease of DTR. The longwave absorption of aerosols can lead to an increase of the daily minimum temperature and contributes to about 20% of the decrease in the DTR. The near-surface air temperature has the largest cooling in the early morning because the ABL is shallow and the temperature is sensitive to the radiative perturbation. As a result of the reduced sensible heat flux, the surface layer becomes more stable. Moreover, the aerosol heating enhances the stabilization of surface layer and in turn further reduces the sensible heat flux. As a result the ABL height can be reduced substantially. This will have many important ramifications, including trapping/accumulation of air pollutants, and perturbing the water

  5. Dense Heavy Metal Aerosol Monitoring by Direct X-Ray Fluorescence

    DTIC Science & Technology

    1989-06-01

    TECHNICAL REPORT BRL-TR-3003 BRL 0 sDENSE HEAVY METAL AEROSOL MONITORING BY DIRECT X-RAY FLUORESCENCE I GEORGE M. THOMSON flgDTIC ELF% CTE b JUN 16...21005-5066 /F 6261A jIN8 1001I 11. TITLE (-’mi- Sawt Cauif&aan)II DENSE HEAVY METAL AEROSOL MONITORMN BY DIRECT X-RAY FLUORESCENCE 12. PERSONAL AUTHOR(S...Before proceeding, a definition of the term "dense, heavy - metal aerosol" is in order. For present purposes, it is an aerosol in which the suspended

  6. Estimates of the direct and indirect radiative forcing due to tropospheric aerosols: A review

    NASA Astrophysics Data System (ADS)

    Haywood, James; Boucher, Olivier

    2000-11-01

    This paper reviews the many developments in estimates of the direct and indirect global annual mean radiative forcing due to present-day concentrations of anthropogenic tropospheric aerosols since Intergovernmental Panel on Climate Change [1996]. The range of estimates of the global mean direct radiative forcing due to six distinct aerosol types is presented. Additionally, the indirect effect is split into two components corresponding to the radiative forcing due to modification of the radiative properties of clouds (cloud albedo effect) and the effects of anthropogenic aerosols upon the lifetime of clouds (cloud lifetime effect). The radiative forcing for anthropogenic sulphate aerosol ranges from -0.26 to -0.82 W m-2. For fossil fuel black carbon the radiative forcing ranges from +0.16 W m-2 for an external mixture to +0.42 W m-2 for where the black carbon is modeled as internally mixed with sulphate aerosol. For fossil fuel organic carbon the two estimates of the likely weakest limit of the direct radiative forcing are -0.02 and -0.04 W m-2. For biomass-burning sources of black carbon and organic carbon the combined radiative forcing ranges from -0.14 to -0.74 W m-2. Estimates of the radiative forcing due to mineral dust vary widely from +0.09 to -0.46 W m-2; even the sign of the radiative forcing is not well established due to the competing effects of solar and terrestrial radiative forcings. A single study provides a very tentative estimate of the radiative forcing of nitrates to be -0.03 W m-2. Estimates of the cloud albedo indirect radiative forcing range from -0.3 to approximately -1.8 W m-2. Although the cloud lifetime effect is identified as a potentially important climate forcing mechanism, it is difficult to quantify in the context of the present definition of radiative forcing of climate change and current model simulations. This is because its estimation by general circulation models necessarily includes some level of cloud and water vapor feedbacks

  7. Water absorption by secondary organic aerosol and its effect on inorganic aerosol behavior

    SciTech Connect

    Ansari, A.S.; Pandis, S.N.

    2000-01-01

    The hygroscopic nature of atmospheric aerosol has generally been associated with its inorganic fraction. In this study, a group contribution method is used to predict the water absorption of secondary organic aerosol (SOA). Compared against growth measurements of mixed inorganic-organic particles, this method appears to provide a first-order approximation in predicting SOA water absorption. The growth of common SOA species is predicted to be significantly less than common atmospheric inorganic salts such as (NH{sub 4}){sub 2}SO{sub 4} and NaCl. Using this group contribution method as a tool in predicting SOA water absorption, an integrated modeling approach is developed combining available SOA and inorganic aerosol models to predict overall aerosol behavior. The effect of SOA on water absorption and nitrate partitioning between the gas and aerosol phases is determined. On average, it appears that SOA accounts for approximately 7% of total aerosol water and increases aerosol nitrate concentrations by approximately 10%. At high relative humidity and low SOA mass fractions, the role of SOA in nitrate partitioning and its contribution to total aerosol water is negligible. However, the water absorption of SOA appears to be less sensitive to changes in relative humidity than that of inorganic species, and thus at low relative humidity and high SOA mass fraction concentrations, SOA is predicted to account for approximately 20% of total aerosol water and a 50% increase in aerosol nitrate concentrations. These findings could improve the results of modeling studies where aerosol nitrate has often been underpredicted.

  8. Volcanic aerosols: Chemistry, evolution, and effects

    NASA Astrophysics Data System (ADS)

    Turco, Richard

    1991-02-01

    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.

  9. 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.

  10. Impact of aerosol radiative effects on 2000-2010 surface temperatures

    NASA Astrophysics Data System (ADS)

    Gettelman, A.; Shindell, D. T.; Lamarque, J. F.

    2015-10-01

    Aerosol radiative forcing from direct and indirect effects of aerosols is examined over the recent past (last 10-15 years) using updated sulfate aerosol emissions in two Earth System Models with very different surface temperature responses to aerosol forcing. The hypothesis is that aerosol forcing and in particular, the impact of indirect effects of aerosols on clouds (Aerosol-Cloud Interactions, or ACI), explains the recent `hiatus' in global mean surface temperature increases. Sulfate aerosol emissions increase globally from 2000 to 2005, and then decrease slightly to 2010. Thus the change in anthropogenic sulfate induced net global radiative forcing is small over the period. Regionally, there are statistically significant forcings that are similar in both models, and consistent with changes in simulated emissions and aerosol optical depth. Coupled model simulations are performed to look at impacts of the forcing on recent surface temperatures. Temperature response patterns in the models are similar, and reflect the regional radiative forcing. Pattern correlations indicate significant correlations between observed decadal surface temperature changes and simulated surface temperature changes from recent sulfate aerosol forcing in an equilibrium framework. Sulfate ACI might be a contributor to the spatial patterns of recent temperature forcing, but not to the global mean `hiatus' itself.

  11. 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.

  12. Reducing the Uncertainties in Direct Aerosol Radiative Forcing

    NASA Technical Reports Server (NTRS)

    Kahn, Ralph A.

    2011-01-01

    Airborne particles, which include desert and soil dust, wildfire smoke, sea salt, volcanic ash, black carbon, natural and anthropogenic sulfate, nitrate, and organic aerosol, affect Earth's climate, in part by reflecting and absorbing sunlight. This paper reviews current status, and evaluates future prospects for reducing the uncertainty aerosols contribute to the energy budget of Earth, which at present represents a leading factor limiting the quality of climate predictions. Information from satellites is critical for this work, because they provide frequent, global coverage of the diverse and variable atmospheric aerosol load. Both aerosol amount and type must be determined. Satellites are very close to measuring aerosol amount at the level-of-accuracy needed, but aerosol type, especially how bright the airborne particles are, cannot be constrained adequately by current techniques. However, satellite instruments can map out aerosol air mass type, which is a qualitative classification rather than a quantitative measurement, and targeted suborbital measurements can provide the required particle property detail. So combining satellite and suborbital measurements, and then using this combination to constrain climate models, will produce a major advance in climate prediction.

  13. A Simple Model of Global Aerosol Indirect Effects

    SciTech Connect

    Ghan, Steven J.; Smith, Steven J.; Wang, Minghuai; Zhang, Kai; Pringle, K. J.; Carslaw, K. S.; Pierce, Jeffrey; Bauer, Susanne E.; Adams, P. J.

    2013-06-28

    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 using analytic representations of droplet nucleation, cloud and aerosol vertical structure, and horizontal variability in cloud water and aerosol concentration. Although the simple model is able to produce estimates of aerosol indirect effects that are comparable to those from some global aerosol models using the same global mean aerosol properties, the estimates are found to be sensitive to several uncertain parameters, including the preindustrial cloud condensation nuclei concentration, primary and secondary anthropogenic emissions, the size of the primary particles, 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. Aerosol indirect effects are surprisingly linear in emissions. This simple model provides a much stronger physical basis for representing aerosol indirect effects than previous representations in integrated assessment models designed to quickly explore the parameter space of emissions-climate interactions. The model also produces estimates that depend on parameter values in ways that are consistent with results from detailed global aerosol-climate simulation models.

  14. Secondary inorganic aerosol formation and its shortwave direct radiative forcing in China

    NASA Astrophysics Data System (ADS)

    Huang, Xin

    2015-04-01

    Secondary inorganic aerosol (SIA), including sulfate, nitrate and ammonium, is an important part of fine particle. SIA plays a significant role in shortwave radiation transfer. Numerical simulation is usually used to study SIA formation and its climate effect. In this work, we used the Weather Research and Forecasting model coupled with Chemistry (WRF-Chem) to study SIA formation and its direct radiative forcing (DRF) over China. SO2 oxidation pathways related to mineral aerosol, including transition metal-catalyzed oxidation in aqueous phase and heterogeneous reactions, play an important role in sulfate production, but they are not well treated in current atmospheric models. In this work, we improved the WRF-Chem model by simulating the enhancement role of mineral aerosol in sulfate production. Firstly, we estimated mineral cations based on local measurements in order to well represent aqueous phase acidity. Secondly, we scaled the transition metal concentration to the mineral aerosol levels according to the existing observations and improved transition metal-catalyzed oxidation calculation. Lastly, heterogeneous reactions of acid gases on the surface of mineral aerosol were included in this simulation. Accuracy in the prediction of sulfate by the model was significantly improved and we concluded that mineral aerosol can facilitate SO2 oxidation and subsequent sulfate formation. It was demonstrated that, over China, mineral aerosol was responsible for 21.8% of annual mean sulfate concentration. The enhanced aqueous oxidation was more significant compared to the heterogeneous reactions. In winter, mineral aerosol was responsible for 39.6% of sulfate production. In summer, gaseous oxidation and aqueous oxidation of SO2 by hydrogen peroxide and ozone were the dominant pathways of sulfate formation. Mineral aerosol only contributed 11.9% to the total sulfate production. The increase in annual mean sulfate concentration due to mineral aerosol could reach up to over 6

  15. 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

    2005-08-09

    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.

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

    PubMed Central

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

    2005-01-01

    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. PMID:16076949

  17. 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.

  18. 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.

  19. 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.

  20. High sensitivity sensor for continuous direct measurement of bipolar charged aerosols

    NASA Astrophysics Data System (ADS)

    Baxter, Karen; Jones, Chris; Fletcher-Wood, Guy

    2008-12-01

    The disruptive generation of aerosols is known to cause particles to carry electrostatic charges. Anthropogenic aerosol may have a standard deviation of charges when generated that is different to other sources or equilibrated aerosols. A simple, low cost 'Bipolar Charged Aerosol Sensor' (BCAS) has been developed to continuously measure charged aerosol in the ambient environment in real-time. Direct measurement of the current released from the charged aerosol particles when they deposit onto an electrode in a DC field is achieved using custom designed, sensitive electrometers. The mobility range of particles collected is defined by the DC field strength, air flow rate through the instrument and the electrode geometry. The mobility range of interest has been selected based on measurements made previously with a complex Laser Doppler Velocimetry (LDV) based instrument. The BCAS has been assessed in laboratory. The sensor design and initial measurement data will be discussed.

  1. Aerosols

    Atmospheric Science Data Center

    2013-04-17

    ... article title:  Aerosols over Central and Eastern Europe     View Larger Image ... last weeks of March 2003, widespread aerosol pollution over Europe was detected by several satellite-borne instruments. The Multi-angle ...

  2. 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.

  3. Effects of aerosols on clear-sky solar radiation in the ALADIN-HIRLAM NWP system

    NASA Astrophysics Data System (ADS)

    Gleeson, Emily; Toll, Velle; Pagh Nielsen, Kristian; Rontu, Laura; Masek, Jan

    2016-05-01

    The direct shortwave radiative effect of aerosols under clear-sky conditions in the Aire Limitee Adaptation dynamique Developpement InterNational - High Resolution Limited Area Model (ALADIN-HIRLAM) numerical weather prediction system was investigated using three shortwave radiation schemes in diagnostic single-column experiments: the Integrated Forecast System (IFS), acraneb2 and the hlradia radiation schemes. The multi-band IFS scheme was formerly used operationally by the European Centre for Medium Range Weather Forecasts (ECMWF) whereas hlradia and acraneb2 are broadband schemes. The former is a new version of the HIRLAM radiation scheme while acraneb2 is the radiation scheme in the ALARO-1 physics package. The aim was to evaluate the strengths and weaknesses of the numerical weather prediction (NWP) system regarding aerosols and to prepare it for use of real-time aerosol information. The experiments were run with particular focus on the August 2010 Russian wildfire case. Each of the three radiation schemes accurately (within ±4 % at midday) simulates the direct shortwave aerosol effect when observed aerosol optical properties are used. When the aerosols were excluded from the simulations, errors of more than +15 % in global shortwave irradiance were found at midday, with the error reduced to +10 % when standard climatological aerosols were used. An error of -11 % was seen at midday if only observed aerosol optical depths at 550 nm, and not observation-based spectral dependence of aerosol optical depth, single scattering albedos and asymmetry factors, were included in the simulations. This demonstrates the importance of using the correct aerosol optical properties. The dependency of the direct radiative effect of aerosols on relative humidity was tested and shown to be within ±6 % in this case. By modifying the assumptions about the shape of the IFS climatological vertical aerosol profile, the inherent uncertainties associated with assuming fixed vertical

  4. Effects of seed aerosols on the growth of secondary organic aerosols from the photooxidation of toluene.

    PubMed

    Hao, Li-qing; Wang, Zhen-ya; Huang, Ming-qiang; Fang, Li; Zhang, Wei-jun

    2007-01-01

    Hydroxyl radical (.OH)-initiated photooxidation reaction of toluene was carried out in a self-made smog chamber. Four individual seed aerosols such as ammonium sulfate, ammonium nitrate, sodium silicate and calcium chloride, were introduced into the chamber to assess their influence on the growth of secondary organic aerosols (SOA). It was found that the low concentration of seed aerosols might lead to high concentration of SOA particles. Seed aerosols would promote rates of SOA formation at the start of the reaction and inhibit its formation rate with prolonging the reaction time. In the case of ca. 9000 pt/cm3 seed aerosol load, the addition of sodium silicate induced a same effect on the SOA formation as ammonium nitrate. The influence of the four individual seed aerosols on the generation of SOA decreased in the order of calcium chloride>sodium silicate and ammonium nitrate>ammonium sulfate.

  5. Direct Aerosol Radiative Forcing Based on Combined A-Train Observations: Towards All-sky Estimates and Attribution to Aerosol Type

    NASA Technical Reports Server (NTRS)

    Redemann, Jens; Shinozuka, Y.; Kacenelenbogen, M.; Russell, P.; Vaughan, M.; Ferrare, R.; Hostetler, C.; Rogers, R.; Burton, S.; Livingston, J.; Torres, O.; Remer, L.

    2014-01-01

    We describe a technique for combining CALIOP aerosol backscatter, MODIS spectral AOD (aerosol optical depth), and OMI AAOD (absorption aerosol optical depth) measurements for the purpose of estimating full spectral sets of aerosol radiative properties, and ultimately for calculating the 3-D distribution of direct aerosol radiative forcing. We present results using one year of data collected in 2007 and show comparisons of the aerosol radiative property estimates to collocated AERONET retrievals. Initial calculations of seasonal clear-sky aerosol radiative forcing based on our multi-sensor aerosol retrievals compare well with over-ocean and top of the atmosphere IPCC-2007 model-based results, and with more recent assessments in the "Climate Change Science Program Report: Atmospheric Aerosol Properties and Climate Impacts" (2009). We discuss some of the challenges that exist in extending our clear-sky results to all-sky conditions. On the basis of comparisons to suborbital measurements, we present some of the limitations of the MODIS and CALIOP retrievals in the presence of adjacent or underlying clouds. Strategies for meeting these challenges are discussed. We also discuss a methodology for using the multi-sensor aerosol retrievals for aerosol type classification based on advanced clustering techniques. The combination of research results permits conclusions regarding the attribution of aerosol radiative forcing to aerosol type.

  6. Analyzing the contribution of aerosols to an observed increase in direct normal irradiance in Oregon

    SciTech Connect

    Riihimaki, L. D.; Vignola, F.; Long, Charles N.

    2009-01-22

    Annual average total irradiance increases by 1-2% per decade at three monitoring stations in Oregon over the period from 1980 to 2007. Direct normal irradiance measurements increase by 5% per decade over the same time period. The measurements show no sign of a dimming before 1990. Clear-sky periods from this long direct normal time series are used in conjunction with radiative transfer calculations to look for changes in anthropogenic aerosols. Stratospheric aerosols from the volcanic eruptions of El Chichon and Mt. Pinatubo are clearly seen in the measurements. The period from 1987 to 2007 shows no detectable change in aerosols not explained by the volcanic aerosols. All three sites show relatively low clear-sky measurements before the eruption of El Chichon in 1982, suggesting higher aerosol loads during this period.

  7. 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.

  8. A global modeling study on carbonaceous aerosol microphysical characteristics and radiative effects

    NASA Astrophysics Data System (ADS)

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

    2010-08-01

    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.

  9. 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.

  10. Direct Radiative Forcing Due to Carbonaceous Aerosols in Biomass Burning Emissions

    NASA Astrophysics Data System (ADS)

    Saleh, R.; Marks, M.; Heo, J.; Adams, P. J.; Donahue, N. M.; Robinson, A. L.

    2014-12-01

    Most climate forcing calculations treat black carbon (BC) as the only carbonaceous particulate light-absorber. Numerous studies have shown that some organic aerosols (OA), mainly associated with biomass burning emissions, contain significant amounts of light-absorbing brown carbon (BrC). However, the light absorption properties of biomass burning OA are poorly constrained, complicating its representation in climate models. During the Fire Laboratory at Missoula Experiment (FLAME 4), we conducted experiments to characterize the light absorption properties of OA in emissions of globally important biomass fuels. We showed that the effective absorptivity of OA depends largely on burn conditions, not fuel type, and derived a parameterization that links OA absorptivity to the BC-to-OA ratio of the emissions (Nature Geoscience, DOI:10.1038/ngeo2220). Here, we utilize this parameterization to estimate the direct radiative effect (DRE) of carbonaceous aerosols in biomass burning emissions using a global chemical transport model (GEOS-Chem) and a column radiative transfer model (libRadTran). The simulations were performed for the year 2005. Monthly-averaged global aerosol concentrations, including BC, OA, inorganic sulfates and nitrates, sea salt, and mineral dust, were obtained from GEOS-Chem simulations. Concentrations of BC and OA from biomass burning emissions were determined by running two GEOS-Chem simulations, one with and one without biomass burning emissions. We attributed the difference in BC and OA concentrations between the two simulations to biomass burning, and could thus calculate the BC-to-OA ratio for biomass burning emissions. libRadTran was used (offline) to calculated DRE due to biomass burning carbonaceous aerosols at each GEOS-Chem grid-cell. Our results show that the global average DRE due to carbonaceous biomass burning emissions increases significantly if light-absorption by OA is considered (using our parameterization for OA absorptivity), compared

  11. A modeling study of the effects of aerosols on clouds and precipitation over East Asia

    NASA Astrophysics Data System (ADS)

    Liu, Xiaodong; Xie, Xiaoning; Yin, Zhi-Yong; Liu, Changhai; Gettelman, Andrew

    2011-12-01

    The National Center for Atmospheric Research Community Atmosphere Model (version 3.5) coupled with the Morrison-Gettelman two-moment cloud microphysics scheme is employed to simulate the aerosol effects on clouds and precipitation in two numerical experiments, one representing present-day conditions (year 2000) and the other the pre-industrial conditions (year 1750) over East Asia by considering both direct and indirect aerosol effects. To isolate the aerosol effects, we used the same set of boundary conditions and only altered the aerosol emissions in both experiments. The simulated results show that the cloud microphysical properties are markedly affected by the increase in aerosols, especially for the column cloud droplet number concentration (DNC), liquid water path (LWP), and the cloud droplet effective radius (DER). With increased aerosols, DNC and LWP have been increased by 137% and 28%, respectively, while DER is reduced by 20%. Precipitation rates in East Asia and East China are reduced by 5.8% and 13%, respectively, by both the aerosol's second indirect effect and the radiative forcing that enhanced atmospheric stability associated with the aerosol direct and first indirect effects. The significant reduction in summer precipitation in East Asia is also consistent with the weakening of the East Asian summer monsoon, resulting from the decreasing thermodynamic contrast between the Asian landmass and the surrounding oceans induced by the aerosol's radiative effects. The increase in aerosols reduces the surface net shortwave radiative flux over the East Asia landmass, which leads to the reduction of the land surface temperature. With minimal changes in the sea surface temperature, hence, the weakening of the East Asian summer monsoon further enhances the reduction of summer precipitation over East Asia.

  12. Impact of the oxidant chemistry description on direct and indirect aerosol forcing estimates

    NASA Astrophysics Data System (ADS)

    Olivié, D.; Sand, M.; Berntsen, T.; Seland; Kirkevåg, A.; Iversen, T.

    2011-12-01

    Sulfate aerosol is formed as a consequence of the oxidation of dimethyl sulfide (DMS) and sulfur dioxide (SO2) by the hydroxyl radical (OH), ozone (O3), hydrogen peroxide (H2O2) and the nitrate radical (NO3). In addition, the amount of particulate organic matter (POM) is also influenced by the atmospheric oxidant concentrations. Oxidant levels can therefore have a considerable impact on aerosols and on their direct and indirect forcing. Here we study the impact of the description of these oxidation reactions. The model which is used is the CAM-Oslo model, which contains an aerosol module describing the evolution of DMS, SO2, sea-salt, dust, BC, POM, and sulfate. It also describes the interaction of the aerosols with radiation and clouds, and therefore gives estimates of the direct and indirect forcing of aerosols. In the standard version of the aerosol module, the oxidation rates are calculated using prescribed monthly fields of OH, O3, H2O2 and NO3. In the new version, we use oxidant fields calculated on-line by a full tropospheric chemistry scheme. On-line OH, O3, H2O2 and NO3 distributions induce both lower sulfate concentrations (-10 %) and lower POM concentrations (-2.5 %). The impact on the direct and indirect forcing is +0.065 and +0.185 W/m2 respectively, underlining the importance of the oxidant description for the estimation of the direct and indirect aerosol forcing.

  13. Satellite Estimates of the Direct Radiative Forcing of Biomass Burning Aerosols Over South America and Africa

    NASA Technical Reports Server (NTRS)

    Christopher, Sundar A.; Wang, Min; Kliche, Donna V.; Berendes, Todd; Welch, Ronald M.; Yang, S.K.

    1997-01-01

    Atmospheric aerosol particles, both natural and anthropogenic are important to the earth's radiative balance. Therefore it is important to provide adequate validation information on the spatial, temporal and radiative properties of aerosols. This will enable us to predict realistic global estimates of aerosol radiative effects more confidently. The current study utilizes 66 AVHRR LAC (Local Area Coverage) and coincident Earth Radiation Budget Experiment (ERBE) images to characterize the fires, smoke and radiative forcings of biomass burning aerosols over four major ecosystems of South America.

  14. Sensitivity of Aerosol Indirect Effects to Representation of Autoconversion

    NASA Astrophysics Data System (ADS)

    Hsieh, W.; Adams, P. J.; Seinfeld, J. H.; Nenes, A.

    2008-12-01

    We study the sensitivity of aerosol indirect effects to the approach used for computing autoconversion of cloudwater into rain. The NASA GISS II-prime GCM, with online simulation of aerosol and cloud droplet number (using the activation parameterization of Fountoukis and Nenes, 2005) are used for simulating the sensitivity of climate and aerosol indirect effects to autoconversion schemes. Simulations are done using the autoconversion parameterizations of Liu and Daum (2004) [P6], Khairoutdinov and Kogan, (2000) [KK], Manton and Cotton, (1977) [MC] and direct integration of the kinetic collection equation (KCE) using a gravitational (GRV) collection kernel with and without enhancement from turbulence (TUR). Given the uncertainty associated with the importance of turbulence on droplet collection, we carry out simulations using two published kernels with substantially different sensitivity to turbulence. Simulations show that increased aerosol associated with anthropogenic activity increase annual mean LWP from changes in autoconversion; strongest effects are seen in highly polluted areas. The spatial distribution of indirect forcing strongly correlates with simulated changes in LWP between pre-industrial and present day simulations; strongest cooling is seen in SE Asia, Western Europe, and eastern US. The combined first and second indirect effect is quite sensitive to the autoconversion scheme used, being -1.30 W m-2 using P6, - 2.05 W m-2 for KK, and, -1.53 W m-2 MC. Using KCE, a smaller indirect effect is simulated, being -0.89 W m- 2 when gravitational collection is only considered, and, equal to -1.03 W m-2 when also enhanced by turbulence. The spatial and temporal distribution of cloud droplet number, effective radius and liquid water content and their sensitivity to the approach used for autoconversion is also assessed.

  15. Effect of environmental factors on aerosol-induced Lassa virus infection.

    PubMed

    Stephenson, E H; Larson, E W; Dominik, J W

    1984-01-01

    Previous studies suggested that the most frequent means of transmission of Lassa virus was by either direct or indirect contact with infectious material. Aerosol stability and respiratory infectivity of the Josiah strain of Lassa virus were assessed to determine the effect of environmental factors on aerosol-induced infection. The stability of the virus in aerosol, particularly at low relative humidity (30% RH), plus the ability of the virus to infect guinea pigs and monkeys via the respiratory route emphasize the potential for aerosol transmission of Lassa virus. Biological half-lives at both 24 and 32 degrees C ranged from 10.1 to 54.6 min, and were sufficient for aerosol dispersion of virus to considerable distances in natural situations. Infectivity of Lassa virus in small particle aerosol was demonstrated in outbred guinea pigs and cynomolgus monkeys using dynamic aerosol equipment. Monkeys exposed to inhaled doses to 465 PFU were infected and died. The median infectious dose (ID50) for guinea pigs was 15 PFU, yet a definitive median lethal aerosol dose (LD50) could not be established. Organ tropism of aerosol-induced Lassa virus infections in outbred guinea pigs was similar to that previously reported for inbred guinea pigs infected by subcutaneous inoculation.

  16. Aerosols and lightning activity: The effect of vertical profile and aerosol type

    NASA Astrophysics Data System (ADS)

    Proestakis, E.; Kazadzis, S.; Lagouvardos, K.; Kotroni, V.; Amiridis, V.; Marinou, E.; Price, C.; Kazantzidis, A.

    2016-12-01

    The Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP) instrument on board the Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observations (CALIPSO) satellite has been utilized for the first time in a study regarding lightning activity modulation due to aerosols. Lightning activity observations, obtained by the ZEUS long range Lightning Detection Network, European Centre for Medium range Weather Forecasts (ECMWF) Convective Available Potential Energy (CAPE) data and Cloud Fraction (CF) retrieved by MODIS on board Aqua satellite have been combined with CALIPSO CALIOP data over the Mediterranean basin and for the period March to November, from 2007 to 2014. The results indicate that lightning activity is enhanced during days characterized by higher Aerosol Optical Depth (AOD) values, compared to days with no lightning. This study contributes to existing studies on the link between lightning activity and aerosols, which have been based just on columnar AOD satellite retrievals, by performing a deeper analysis into the effect of aerosol profiles and aerosol types. Correlation coefficients of R = 0.73 between the CALIPSO AOD and the number of lightning strikes detected by ZEUS and of R = 0.93 between ECMWF CAPE and lightning activity are obtained. The analysis of extinction coefficient values at 532 nm indicates that at an altitudinal range exists, between 1.1 km and 2.9 km, where the values for extinction coefficient of lightning-active and non-lightning-active cases are statistically significantly different. Finally, based on the CALIPSO aerosol subtype classification, we have investigated the aerosol conditions of lightning-active and non-lightning-active cases. According to the results polluted dust aerosols are more frequently observed during non-lightning-active days, while dust and smoke aerosols are more abundant in the atmosphere during the lightning-active days.

  17. The Invigoration of Deep Convective Clouds Over the Atlantic: Aerosol Effect, Meteorology or Retrieval Artifact?

    NASA Technical Reports Server (NTRS)

    Koren, Ilan; Feingold, Graham; Remer, Lorraine A.

    2010-01-01

    Associations between cloud properties and aerosol loading are frequently observed in products derived from satellite measurements. These observed trends between clouds and aerosol optical depth suggest aerosol modification of cloud dynamics, yet there are uncertainties involved in satellite retrievals that have the potential to lead to incorrect conclusions. Two of the most challenging problems are addressed here: the potential for retrieved aerosol optical depth to be cloud-contaminated, and as a result, artificially correlated with cloud parameters; and the potential for correlations between aerosol and cloud parameters to be erroneously considered to be causal. Here these issues are tackled directly by studying the effects of the aerosol on convective clouds in the tropical Atlantic Ocean using satellite remote sensing, a chemical transport model, and a reanalysis of meteorological fields. Results show that there is a robust positive correlation between cloud fraction or cloud top height and the aerosol optical depth, regardless of whether a stringent filtering of aerosol measurements in the vicinity of clouds is applied, or not. These same positive correlations emerge when replacing the observed aerosol field with that derived from a chemical transport model. Model-reanalysis data is used to address the causality question by providing meteorological context for the satellite observations. A correlation exercise between the full suite of meteorological fields derived from model reanalysis and satellite-derived cloud fields shows that observed cloud top height and cloud fraction correlate best with model pressure updraft velocity and relative humidity. Observed aerosol optical depth does correlate with meteorological parameters but usually different parameters from those that correlate with observed cloud fields. The result is a near-orthogonal influence of aerosol and meteorological fields on cloud top height and cloud fraction. The results strengthen the case

  18. Intercomparison of Models Representing Direct Shortwave Radiative Forcing by Sulfate Aerosols

    NASA Technical Reports Server (NTRS)

    Boucher, O.; Schwartz, S. E.; Ackerman, T. P.; Anderson, T. L.; Bergstrom, B.; Bonnel, B.; Dahlback, A.; Fouquart, Y.; Chylek, P.; Fu, Q.; Halthore, R. N.; Haywood, J. M.; Iversen, T.; Kato, S.; Kinne, S.; Kirkevag, A.; Knapp, K. R.; Lacis, A.; Laszlo, I.; Mishchenko, M. I.

    2000-01-01

    The importance of aerosols as agents of climate change has recently been highlighted. However, the magnitude of aerosol forcing by scattering of shortwave radiation (direct forcing) is still very uncertain even for the relatively well characterized sulfate aerosol. A potential source of uncertainty is in the model representation of aerosol optical properties and aerosol influences on radiative transfer in the atmosphere. Although radiative transfer methods and codes have been compared in the past, these comparisons have not focused on aerosol forcing (change in net radiative flux at the top of the atmosphere). Here we report results of a project involving 12 groups using 15 models to examine radiative forcing by sulfate aerosol for a wide range of values of particle radius, aerosol optical depth, surface albedo, and solar zenith angle. Among the models that were employed were high and low spectral resolution models incorporating a variety of radiative transfer approximations as well as a line-by-line model. The normalized forcings (forcing per sulfate column burden) obtained with the several radiative transfer models were examined, and the discrepancies were characterized. All models simulate forcings of comparable amplitude and exhibit a similar dependence on input parameters. As expected for a non-light-absorbing aerosol, forcings were negative (cooling influence) except at high surface albedo combined with small solar zenith angle. The relative standard deviation of the zenith-angle-averaged normalized broadband forcing for 15 models-was 8% for particle radius near the maximum in this forcing (approx. 0.2 microns) and at low surface albedo. Somewhat greater model-to-model discrepancies were exhibited at specific solar zenith angles. Still greater discrepancies were exhibited at small particle radii and much greater discrepancies were exhibited at high surface albedos, at which the forcing changes sign; in these situations, however, the normalized forcing is

  19. 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

  20. The effect of volcanic aerosols on ultraviolet radiation in Antarctica

    NASA Astrophysics Data System (ADS)

    Tsitas, Steven R.; Yung, Yuk L.

    Volcanic eruptions can inject large amounts of aerosol into the atmosphere, and, at large solar zenith angles, scattering by these aerosols can actually increase the flux of UV-B (290-320 nm) radiation reaching the surface. This is surprising since aerosols increase the reflection of sunlight to space. As previous explanations of this phenomenon are heuristic and incomplete, we first provide a rigorous and complete explanation of how this surprising effect occurs. This phenomenon makes Antarctica during spring the most susceptible place on Earth to the scattering effect of volcanic aerosols, due to the combined effect of the spring ozone hole and the large solar zenith angles characteristic of this time of year. We show that an aerosol layer lying above Antarctica during spring will decrease the integrated daily dose of biologically weighted irradiance, weighted by the erythema action spectrum, by only up to 5%. Hence the effects of any significant destruction of ozone induced by volcanic aerosols will not be offset by aerosol scattering. Thus after a volcanic eruption, life in Antarctica during spring will suffer the combined effects of the spring ozone hole and ozone destruction induced by volcanic aerosols, with the latter effect only slightly offset by aerosol scattering.

  1. A new chemistry option in WRF-Chem v. 3.4 for the simulation of direct and indirect aerosol effects using VBS: evaluation against IMPACT-EUCAARI data

    NASA Astrophysics Data System (ADS)

    Tuccella, P.; Curci, G.; Grell, G. A.; Visconti, G.; Crumeyrolle, S.; Schwarzenboeck, A.; Mensah, A. A.

    2015-09-01

    condensation nuclei (CCN) are also overestimated, but the bias is more contained with respect to that of CN. The CCN efficiency, which is a characterization of the ability of aerosol particles to nucleate cloud droplets, is underestimated by a factor of 1.5 and 3.8 in the PBL and FT, respectively. The comparison with MODIS data shows that the model overestimates the aerosol optical thickness (AOT). The domain averages (for 1 day) are 0.38 ± 0.12 and 0.42 ± 0.10 for MODIS and WRF-Chem data, respectively. The droplet effective radius (Re) in liquid-phase clouds is underestimated by a factor of 1.5; the cloud liquid water path (LWP) is overestimated by a factor of 1.1-1.6. The consequence is the overestimation of average liquid cloud optical thickness (COT) from a few percent up to 42 %. The predicted cloud water path (CWP) in all phases displays a bias in the range +41-80 %, whereas the bias of COT is about 15 %. In sensitivity tests where we excluded SOA, the skills of the model in reproducing the observed patterns and average values of the microphysical and optical properties of liquid and all phase clouds decreases. Moreover, the run without SOA (NOSOA) shows convective clouds with an enhanced content of liquid and frozen hydrometers, and stronger updrafts and downdrafts. Considering that the previous version of WRF-Chem coupled with a modal aerosol module predicted very low SOA content (secondary organic aerosol model (SORGAM) mechanism) the new proposed option may lead to a better characterization of aerosol-cloud feedbacks.

  2. 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.

  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

    radiative properties to aerosol composition, size distribution, relative humidity (RH) is examined for the following aerosol systems: inorganic and organic ions (Cl-, Br-, NO3 -, SO4 2-, Na+, NH4 +, K+, Ca2+, Mg2+, HCOO-, CH3COO-, CH3CH2COO-, CH3COCOO-, OOCCOO2-, MSA-1); water-insoluble inorganic and organic compounds (elemental carbon, n-alkanes, SiO2, Al2O3, Fe2O3 and other organic compounds). The partial molar refraction method was used to calculate the real part of the refractive index. It was found that the asymmetry factor increased by approximately 48% with the real part varying from 1.40 to 1.65, and the single scattering albedo decreased by 24% with the imaginary part varying from -0.005 to -0.1. The asymmetry factor increased by 5.4 times with the geometric standard deviation varying from 1.2 to 3.0. The radiation transmission is very sensitive to the change in size distribution; other factors are not as significant. To determine the aerosol direct radiative forcing (ADRF), the aerosol optical depth (AOD) values at the three operational wavelengths (415, 500 and 673 nm) were determined at a regionally representative site, namely, Mt. Gibbs (35.78 deg N, 82.29 deg W, elevation 2006 m) in Mt. Mitchell State Park, NC, and a site located in an adjacent valley (Black Mountain, 35.66 deg N, 82.38 deg W, elevation 951 m) in the southeastern US. The two sites are separated horizontally by 10 km and vertically by 1 km. It was found that the representative total AOD values at 500 nm at the valley site for highly polluted (HP), marine (M) and continental (C) air masses were 0.68 +/- 0.33, 0.29 +/- 0.19 and 0.10 +/- 0.04, respectively. A search-graph method was used to retrieve the columnar size distribution (number concentration N, effective radius reff and geometric standard deviation=?g) from the optical depth observations at three operational wavelengths. The ground albedo, single scattering albedo and imaginary part of the refractive index were calculated using a

  4. Quantifying the climatological cloud-free shortwave direct radiative forcing of mineral dust aerosol over the Red Sea

    NASA Astrophysics Data System (ADS)

    Stenchikov, G. L.; Brindley, H. E.; Osipov, S.; Bantges, R. J.; Smirnov, A.; Prakash, P. J.

    2014-12-01

    While there have been a number of campaigns designed to probe dust-climate interactions over much of the world, relatively little attention has been paid to the Red Sea. Because of the remoteness of the area, satellite retrievals provide a crucial tool for assessing aerosol loading over the Sea. However, agreement between aerosol properties inferred from measurements from different instruments, and even in some cases from the same measurements using different retrieval algorithms can be poor, particularly in the case of mineral dust. Ground based measurements, which can be used to evaluate retrievals, are thus highly desirable. Here we take advantage of ship-based hand-held sun-photometer (microtops) observations gathered within the framework of NASA Aerosol Maritime Network from a series of cruises, which took place across the Red Sea during 2011 and 2013. To our knowledge these data represent the first set of detailed aerosol measurements from the Sea. They thus provide a unique opportunity to assess the performance of satellite retrieval algorithms in this region. Here we used the microtops measurements to evaluate the performance of co-located satellite retrievals from the Spinning Enhanced Visible and InfraRed Imager (SEVIRI) and the MODerate Imaging Spectrometer (MODIS). Both algorithms show good agreement with the ship-based measurements and with each other, although it appears that the MODIS cloud detection scheme in particular is rather conservative. The stand alone Rapid Radiative Transfer Model (RRTM) driven by reanalysis meteorological fields is used to estimate the cloud-free aerosol direct radiative effect at the surface and TOA along the ship tracks. The TOA effects are compared to co-located measurements from the Geostationary Earth Radiation Budget (GERB) instrument. Having evaluated both the quality of the retrievals and the ability of the model to capture the associated radiative effect, we will present a climatology of aerosol loading over the

  5. The Effects of Transpacific Transported Aerosol on Clouds in California

    NASA Astrophysics Data System (ADS)

    Suski, K.; Creamean, J.; Rosenfeld, D.; Cazorla, A.; DeMott, P. J.; Sullivan, R. C.; White, A. B.; Ralph, F. M.; Cahill, J.; Tomlinson, J. M.; Chand, D.; Schmid, B.; Prather, K. A.

    2012-12-01

    Atmospheric aerosols are frequently lofted high into the atmosphere and can travel large distances within several days. Long-range transported aerosols can have large impacts on radiative and microphysical cloud properties and can affect precipitation on both regional and global scales. Research flights were conducted out of Sacramento, California onboard the DOE G-1 aircraft during the CalWater 2011 flight campaign, which aimed to understand the effects of aerosols on clouds and precipitation in California. To investigate aerosol effects on clouds, measurements of cloud microphysical properties were coupled with an aircraft aerosol time-of-flight mass spectrometer (A-ATOFMS), which characterized the chemical composition of aerosols and cloud residues. California Central Valley pollution aerosols were hypothesized to have a large impact on orographic clouds in the California Sierra Nevada Mountains; however transpacific transported aerosols were observed in cloud residues on several flights. Our observations indicate that dust from Asia, Africa, and the Middle East initiated ice formation in upper level clouds, while Asian soot from biomass burning served as cloud condensation nuclei in clouds with large concentrations of small liquid droplets. Previous work has linked large concentrations of small droplets to suppression of orographic precipitation, while ice formation has been shown to enhance precipitation. Therefore, the overall impact of these competing effects on precipitation in the Sierra Nevada is highly uncertain. The varying impacts of long-range transported aerosols on clouds and precipitation in California are presented.

  6. Direct lung delivery of a dry powder formulation of DTPA with improved aerosolization properties: effect on lung and systemic decorporation of plutonium.

    PubMed

    Gervelas, C; Serandour, A-L; Geiger, S; Grillon, G; Fritsch, P; Taulelle, C; Le Gall, B; Benech, H; Deverre, J-R; Fattal, E; Tsapis, N

    2007-03-12

    DTPA, an actinide chelating agent, has demonstrated its ability to complex plutonium (Pu) and to facilitate its urinary excretion after internal contamination. This process, known as decorporation is crucial to diminish the burden of Pu in the body. The ability to deliver a chelating agent directly to the alveolar region may increase its local concentration as compared to systemic delivery and therefore increase the extent of decorporation. Second, inhalation offers the potential for needle-free, systemic delivery of small molecules and would be convenient in case of nuclear accident as a first pass emergency treatment. To benefit from the improvement of inhalation technology, we have formulated DTPA into porous particles by spray-drying with dl-Leucine, DPPC and ammonium bicarbonate. The optimized particles possess a volume mean geometric diameter around 4.5 mum and crumpled paper morphology. The in vitro aerodynamic evaluation shows that about 56% of the powder should deposits in the lungs, with about 27% in the alveolar region, an improvement as compared with the micronized powder available with the Spinhaler. After pulmonary administration to rats contaminated with PuO(2), a 3-fold increase of the Pu urinary excretion was observed, but the dissolution of PuO(2) in the lungs was not enhanced.

  7. New Satellite Measurements of Aerosol Direct Radiative Forcing from MODIS, MISR, and POLDER

    NASA Technical Reports Server (NTRS)

    Kaufman, Y.

    2000-01-01

    New set of satellites, MODIS and MISR launched on EOS-Terra and POLDER launched on ADEOS-1, and scheduled for ADEOS-II and PARASOL in orbit with EOS-AQUA, open exciting opportunities to measure aerosol and their radiative forcing of climate. Each of these instruments has a different approach to invert remote sensing data to derive the aerosol properties. MODIS is using wide spectral range 0.47-2.1 micron. MISR is using narrower spectral range (0.44 to 0.87 micron) but observing the same spot from 9 different angles along the satellite track. POLDER using similar wavelengths, uses two dimensional view with a wide angle optics and adds polarization to the inversion process. Among these instruments, we expect to measure the global distribution of aerosol, to distinguish small pollution particles from large particles from deserts and ocean spray. We shall try to measure the aerosol absorption of solar radiation, and their refractive index that indicates the effect of liquid water on the aerosol size and interaction with sunlight. The radiation field measured by these instruments in variety of wavelengths and angles, is also used to derive the effect of the aerosol on reflection of sunlight spectral fluxes to space. When combined with flux measurements at the ground, it gives a complete characterization of the effect of aerosol on solar illumination, heating in the atmosphere and reflection to space.

  8. Evolution of ozone, particulates, and aerosol direct radiative forcing in the vicinity of Houston using a fully coupled meteorology-chemistry-aerosol model

    NASA Astrophysics Data System (ADS)

    Fast, Jerome D.; Gustafson, William I.; Easter, Richard C.; Zaveri, Rahul A.; Barnard, James C.; Chapman, Elaine G.; Grell, Georg A.; Peckham, Steven E.

    2006-11-01

    A new fully coupled meteorology-chemistry-aerosol model is used to simulate the urban- to regional-scale variations in trace gases, particulates, and aerosol direct radiative forcing in the vicinity of Houston over a 5 day summer period. Model performance is evaluated using a wide range of meteorological, chemistry, and particulate measurements obtained during the 2000 Texas Air Quality Study. The predicted trace gas and particulate distributions were qualitatively similar to the surface and aircraft measurements with considerable spatial variations resulting from urban, power plant, and industrial sources of primary pollutants. Sulfate, organic carbon, and other inorganics were the largest constituents of the predicted particulates. The predicted shortwave radiation was 30 to 40 W m-2 closer to the observations when the aerosol optical properties were incorporated into the shortwave radiation scheme; however, the predicted hourly aerosol radiative forcing was still underestimated by 10 to 50 W m-2. The predicted aerosol radiative forcing was larger over Houston and the industrial ship channel than over the rural areas, consistent with surface measurements. The differences between the observed and simulated aerosol radiative forcing resulted from transport errors, relative humidity errors in the upper convective boundary layer that affect aerosol water content, secondary organic aerosols that were not yet included in the model, and uncertainties in the primary particulate emission rates. The current model was run in a predictive mode and demonstrates the challenges of accurately simulating all of the meteorological, chemical, and aerosol parameters over urban to regional scales that can affect aerosol radiative forcing.

  9. Influence of the vertical absorption profile of mixed Asian dust plumes on aerosol direct radiative forcing over East Asia

    NASA Astrophysics Data System (ADS)

    Noh, Young Min; Lee, Kwonho; Kim, Kwanchul; Shin, Sung-Kyun; Müller, Detlef; Shin, Dong Ho

    2016-08-01

    We estimate the aerosol direct radiative forcing (ADRF) and heating rate profiles of mixed East Asian dust plumes in the solar wavelength region ranging from 0.25 to 4.0 μm using the Santa Barbara Discrete Ordinate Atmospheric Radiative Transfer (SBDART) code. Vertical profiles of aerosol extinction coefficients and single-scattering albedos (SSA) were derived from measurements with a multi-wavelength Raman lidar system. The data are used as input parameters for our radiative transfer calculations. We considered four cases of radiative forcing in SBDART: 1. dust, 2. pollution, 3. mixed dust plume and the use of vertical profiles of SSA, and 4. mixed dust plumes and the use of column-averaged values of SSA. In our sensitivity study we examined the influence of SSA and aerosol layer height on our results. The ADRF at the surface and in the atmosphere shows a small dependence on the specific shape of the aerosol extinction vertical profile and its light-absorption property for all four cases. In contrast, at the top of the atmosphere (TOA), the ADRF is largely affected by the vertical distribution of the aerosols extinction. This effect increases if the light-absorption capacity (decrease of SSA) of the aerosols increases. We find different radiative effects in situations in which two layers of aerosols had different light-absorption properties. The largest difference was observed at the TOA for an absorbing aerosol layer at high altitude in which we considered in one case the vertical profile of SSA and in another case the column-averaged SSA only. The ADRF at the TOA increases when the light-absorbing aerosol layer is located above 3 km altitude. The differences between height-resolved SSA, which can be obtained from lidar data, and total layer-mean SSA indicates that the use of a layer-mean SSA can be rather misleading as it can induce a large error in the calculation of the ADRF at the TOA, which in turn may cause errors in the vertical profiles of heating rates.

  10. 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.

  11. Aerosol, Cloud and Trace Gas Observations Derived from Airborne Hyperspectral Radiance and Direct Beam Measurements in Recent Field Campaigns

    NASA Technical Reports Server (NTRS)

    Redemann, J.; Flynn, C. J.; Shinozuka, Y.; Kacenelenbogen, M.; Segal-Rosenheimer, M.; LeBlanc, S.; Russell, P. B.; Livingston, J. M.; Schmid, B.; Dunagan, S. E.; Johnson, R. R.

    2014-01-01

    The AERONET (AErosol RObotic NETwork) ground-based suite of sunphotometers provides measurements of spectral aerosol optical depth (AOD), precipitable water and spectral sky radiance, which can be inverted to retrieve aerosol microphysical properties that are critical to assessments of aerosol-climate interactions. Because of data quality criteria and sampling constraints, there are significant limitations to the temporal and spatial coverage of AERONET data and their representativeness for global aerosol conditions. The 4STAR (Spectrometer for Sky-Scanning, Sun-Tracking Atmospheric Research) instrument, jointly developed by NASA Ames and PNNL with NASA Goddard collaboration, combines airborne sun tracking and AERONET-like sky scanning with spectroscopic detection. Being an airborne instrument, 4STAR has the potential to fill gaps in the AERONET data set. Dunagan et al. [2013] present results establishing the performance of the instrument, along with calibration, engineering flight test, and preliminary scientific field data. The 4STAR instrument operated successfully in the SEAC4RS [Studies of Emissions and Atmospheric Composition, Clouds and Climate Coupling by Regional Surveys] experiment in Aug./Sep. 2013 aboard the NASA DC-8 and in the DoE [Department of Energy]-sponsored TCAP [Two Column Aerosol Project, July 2012 & Feb. 2013] experiment aboard the DoE G-1 aircraft (Shinozuka et al., 2013), and acquired a wealth of data in support of mission objectives on all SEAC4RS and TCAP research flights. 4STAR provided direct beam measurements of hyperspectral AOD, columnar trace gas retrievals (H2O, O3, NO2; Segal-Rosenheimer et al., 2014), and the first ever airborne hyperspectral sky radiance scans, which can be inverted to yield the same products as AERONET ground-based observations. In addition, 4STAR measured zenith radiances underneath cloud decks for retrievals of cloud optical depth and effective diameter. In this presentation, we provide an overview of the new

  12. 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

  13. Direct aerosol chemical composition measurements to evaluate the physicochemical differences between controlled sea spray aerosol generation schemes

    NASA Astrophysics Data System (ADS)

    Collins, D. B.; Zhao, D. F.; Ruppel, M. J.; Laskina, O.; Grandquist, J. R.; Modini, R. L.; Stokes, M. D.; Russell, L. M.; Bertram, T. H.; Grassian, V. H.; Deane, G. B.; Prather, K. A.

    2014-11-01

    Controlled laboratory studies of the physical and chemical properties of sea spray aerosol (SSA) must be under-pinned by a physically and chemically accurate representation of the bubble-mediated production of nascent SSA particles. Bubble bursting is sensitive to the physico-chemical properties of seawater. For a sample of seawater, any important differences in the SSA production mechanism are projected into the composition of the aerosol particles produced. Using direct chemical measurements of SSA at the single-particle level, this study presents an intercomparison of three laboratory-based, bubble-mediated SSA production schemes: gas forced through submerged sintered glass filters ("frits"), a pulsed plunging-waterfall apparatus, and breaking waves in a wave channel filled with natural seawater. The size-resolved chemical composition of SSA particles produced by breaking waves is more similar to particles produced by the plunging waterfall than those produced by sintered glass filters. Aerosol generated by disintegrating foam produced by sintered glass filters contained a larger fraction of organic-enriched particles and a different size-resolved elemental composition, especially in the 0.8-2 μm dry diameter range. Interestingly, chemical differences between the methods only emerged when the particles were chemically analyzed at the single-particle level as a function of size; averaging the elemental composition of all particles across all sizes masked the differences between the SSA samples. When dried, SSA generated by the sintered glass filters had the highest fraction of particles with spherical morphology compared to the more cubic structure expected for pure NaCl particles produced when the particle contains relatively little organic carbon. In addition to an intercomparison of three SSA production methods, the role of the episodic or "pulsed" nature of the waterfall method on SSA composition was under-taken. In organic-enriched seawater, the continuous

  14. On the influence of the diurnal variations of aerosol content to estimate direct aerosol radiative forcing using MODIS data

    NASA Astrophysics Data System (ADS)

    Xu, Hui; Guo, Jianping; Ceamanos, Xavier; Roujean, Jean-Louis; Min, Min; Carrer, Dominique

    2016-09-01

    Long-term measurements of aerosol optical depth (AOD) from the Aerosol Robotic Network (AERONET) located in Beijing reveal a strong diurnal cycle of aerosol load staged by seasonal patterns. Such pronounced variability is matter of importance in respect to the estimation of daily averaged direct aerosol radiative forcing (DARF). Polar-orbiting satellites could only offer a daily revisit, which turns in fact to be even much less in case of frequent cloudiness. Indeed, this places a severe limit to properly capture the diurnal variations of AOD and thus estimate daily DARF. Bearing this in mind, the objective of the present study is however to evaluate the impact of AOD diurnal variations for conducting quantitative assessment of DARF using Moderate Resolution Imaging Spectroradiometer (MODIS) AOD data over Beijing. We provide assessments of DARF with two different assumptions about diurnal AOD variability: taking the observed hourly-averaged AOD cycle into account and assuming constant MODIS (including Terra and Aqua) AOD value throughout the daytime. Due to the AOD diurnal variability, the absolute differences in annual daily mean DARFs, if the constant MODIS/Terra (MODIS/Aqua) AOD value is used instead of accounting for the observed hourly-averaged daily variability, is 1.2 (1.3) Wm-2 at the top of the atmosphere, 27.5 (30.6) Wm-2 at the surface, and 26.4 (29.3) Wm-2 in the atmosphere, respectively. During the summertime, the impact of the diurnal AOD variability on seasonal daily mean DARF estimates using MODIS Terra (Aqua) data can reach up to 2.2 (3.9) Wm-2 at the top of the atmosphere, 43.7 (72.7) Wm-2 at the surface, and 41.4 (68.8) Wm-2 in the atmosphere, respectively. Overall, the diurnal variation in AOD tends to cause large bias in the estimated DARF on both seasonal and annual scales. In summertime, the higher the surface albedo, the stronger impact on DARF at the top of the atmosphere caused by dust and biomass burning (continental) aerosol. This

  15. Aerosol direct radiative forcing in desert and semi-desert regions of northwestern China

    NASA Astrophysics Data System (ADS)

    Xin, Jinyuan; Gong, Chongshui; Wang, Shigong; Wang, Yuesi

    2016-05-01

    The optical properties of dust aerosols were measured using narrow-band data from a portable sun photometer at four desert and semi-desert stations in northwestern China from 2004 to 2007. Ground-based and satellite observations indicated absorbing dust aerosol loading over the region surrounded by eight large-scale deserts. Radiation forcing was identified by using the Santa Barbara DISORT Atmospheric Radiative Transfer (SBDART) model. The ranges of annual mean aerosol optical depth (AOD), Angström exponents, and single-scattering albedo (SSA) were from 0.25 to 0.35, from - 0.73 to 1.18, and from 0.77 to 0.86, respectively. The ranges of annual mean aerosol direct radiative forcing values at the top of the atmosphere (TOA), mid-atmosphere, and on the surface were from 3.9 to 12.0, from 50.0 to 53.1, and from - 39.1 to - 48.1 W/m2, respectively. The aerosols' optical properties and radiative characteristics showed strong seasonal variations in both the desert and semi-desert regions. Strong winds and relatively low humidity will lead dust aerosols in the atmosphere to an increase, which played greatly affected these optical properties during spring and winter in northwestern China. Based on long-term observations and retrieved data, aerosol direct radiative forcing was confirmed to heat the atmosphere (50-53 W/m2) and cool the surface (- 39 to - 48 W/m2) above the analyzed desert. Radiative forcing in the atmosphere in spring and winter was 18 to 21 W/m2 higher than other two seasons. Based on the dust sources around the sites, the greater the AOD, the more negative the forcing. The annual averaged heating rates for aerosols close to the ground (1 km) were approximately 0.80-0.85 K/day.

  16. 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.

  17. Radiative effects of interannually varying vs. interannually invariant aerosol emissions from fires

    NASA Astrophysics Data System (ADS)

    Grandey, Benjamin S.; Lee, Hsiang-He; Wang, Chien

    2016-11-01

    Open-burning fires play an important role in the earth's climate system. In addition to contributing a substantial fraction of global emissions of carbon dioxide, they are a major source of atmospheric aerosols containing organic carbon, black carbon, and sulfate. These "fire aerosols" can influence the climate via direct and indirect radiative effects. In this study, we investigate these radiative effects and the hydrological fast response using the Community Atmosphere Model version 5 (CAM5). Emissions of fire aerosols exert a global mean net radiative effect of -1.0 W m-2, dominated by the cloud shortwave response to organic carbon aerosol. The net radiative effect is particularly strong over boreal regions. Conventionally, many climate modelling studies have used an interannually invariant monthly climatology of emissions of fire aerosols. However, by comparing simulations using interannually varying emissions vs. interannually invariant emissions, we find that ignoring the interannual variability of the emissions can lead to systematic overestimation of the strength of the net radiative effect of the fire aerosols. Globally, the overestimation is +23 % (-0.2 W m-2). Regionally, the overestimation can be substantially larger. For example, over Australia and New Zealand the overestimation is +58 % (-1.2 W m-2), while over Boreal Asia the overestimation is +43 % (-1.9 W m-2). The systematic overestimation of the net radiative effect of the fire aerosols is likely due to the non-linear influence of aerosols on clouds. However, ignoring interannual variability in the emissions does not appear to significantly impact the hydrological fast response. In order to improve understanding of the climate system, we need to take into account the interannual variability of aerosol emissions.

  18. Quantifying the Indirect Effect of Sulfate Aerosol on Climate Change Through the Carbon Cycle

    NASA Astrophysics Data System (ADS)

    Cadule, P.; Friedlingstein, P.; Bopp, L.; Piao, S.; Ciais, P.

    2008-12-01

    Elevated atmospheric concentrations of greenhouse gases will continue to warm the Earth's climate in the coming century. Coupled climate-carbon models have demonstrated a significant climate-induced reduction of natural carbon sinks, which acts as a positive feedback on the atmospheric CO2 concentration (between +20 and +220 ppm in 2100, for the SRES A2 emission scenario). Sulfate aerosols are known to affect climate through a radiative direct effect and a series of indirect effects involving the atmospheric water cycle. However, the effects of sulfate aerosols and non-CO2 greenhouse gases were neglected in these coupled climate-carbon cycle models. Here we performed new coupled climate-carbon simulations wherein the evolution of sulfate aerosols and non-CO2 greenhouse gases were explicitly represented. We show a hitherto undocumented indirect effect of aerosols on climate, via the carbon cycle. While sulfate aerosols cool the climate by 0.79°C globally, this cooling reduces land carbon sinks, leaving additional CO2 in the atmosphere. At mid-to-high northern latitudes, the aerosol-induced cooling is responsible for a decline in photosynthesis and land carbon uptake (-63 PgC by 2100). On the other hand, a variety of processes yields increased tropical carbon uptake (+28 PgC) in response to aerosol induced cooling, which is insufficient to balance the decline in the northern hemisphere. Overall, including non- CO2 greenhouse gases and sulfate aerosols, in coupled simulations, doubles the additional quantity of CO2 accumulating in the atmosphere due to climate change. Our results demonstrate that any climate mitigation policy that aims to reduce warming via sulfate aerosols must also account for their indirect warming effect, which arises from interactions between climate and the carbon cycle.

  19. 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...

  20. 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...

  1. The effect of subtropical aerosol loading on equatorial precipitation

    NASA Astrophysics Data System (ADS)

    Dagan, G.; Chemke, R.

    2016-10-01

    Cloud-aerosol interactions are considered as one of the largest sources of uncertainties in the study of climate change. Here another possible cloud-aerosol effect on climate is proposed. A series of large eddy simulations (LES) with bin microphysics reveal a sensitivity of the total atmospheric water vapor amount to aerosol concentration. Under polluted conditions the rain is suppressed and the total amount of water vapor in the atmosphere increases with time compared to clean precipitating conditions. Theoretical examination of this aerosol effect on water vapor transport from the subtropics to the tropics, and hence on the equatorial rain and Hadley circulation, is conducted using an idealized general circulation model (GCM). It is shown that a reduction in the subtropical rain amount results in increased water vapor advection to the tropics and enhanced equatorial rain and Hadley circulation. This joins previously proposed mechanisms on the radiative aerosol effect on the general circulation.

  2. Influence of atmospheric relative humidity on ultraviolet flux and aerosol direct radiative forcing: Observation and simulation

    NASA Astrophysics Data System (ADS)

    Xia, Dong; Chen, Ling; Chen, Huizhong; Luo, Xuyu; Deng, Tao

    2016-08-01

    The atmospheric aerosols can absorb moisture from the environment due to their hydrophilicity and thus affect atmospheric radiation fluxes. In this article, the ultraviolet radiation and relative humidity (RH) data from ground observations and a radiative transfer model were used to examine the influence of RH on ultraviolet radiation flux and aerosol direct radiative forcing under the clear-sky conditions. The results show that RH has a significant influence on ultraviolet radiation because of aerosol hygroscopicity. The relationship between attenuation rate and RH can be fitted logarithmically and all of the R2 of the 4 sets of samples are high, i.e. 0.87, 0.96, 0.9, and 0.9, respectively. When the RH is 60%, 70%, 80% and 90%, the mean aerosol direct radiative forcing in ultraviolet is -4.22W m-2, -4.5W m-2, -4.82W m-2 and -5.4W m-2, respectively. For the selected polluted air samples the growth factor for computing aerosol direct radiative forcing in the ultraviolet for the RH of 80% varies from 1.19 to 1.53, with an average of 1.31.

  3. 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

  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. Reallocation in modal aerosol models: impacts on predicting aerosol radiative effects

    NASA Astrophysics Data System (ADS)

    Korhola, T.; Kokkola, H.; Korhonen, H.; Partanen, A.-I.; Laaksonen, A.; Lehtinen, K. E. J.; Romakkaniemi, S.

    2014-01-01

    Atmospheric models often represent the aerosol particle size distribution with a modal approach, in which particles are described with log-normal modes within predetermined size ranges. This approach reallocates particles numerically from one mode to another for example during particle growth, potentially leading to artificial changes in the aerosol size distribution. In this study we analysed how the modal reallocation affects climate-relevant variables: cloud droplet number concentration (CDNC), aerosol-cloud interaction parameter (ACI) and light extinction coefficient (qext). The ACI parameter gives the response of CDNC to a change in total aerosol number concentration. We compared these variables between a modal model (with and without reallocation routines) and a high resolution sectional model, which was considered a reference model. We analysed the relative differences in the chosen variables in four experiments designed to assess the influence of atmospheric aerosol processes. We find that limiting the allowed size ranges of the modes, and subsequent remapping of the distribution, leads almost always to an underestimation of cloud droplet number concentrations (by up to 100%) and an overestimation of light extinction (by up to 20%). On the other hand, the aerosol-cloud interaction parameter can be either over- or underestimated by the reallocating model, depending on the conditions. For example, in the case of atmospheric new particle formation events followed by rapid particle growth, the reallocation can cause on average a 10% overestimation of the ACI parameter. Thus it is shown that the reallocation affects the ability of a model to estimate aerosol climate effects accurately, and this should be taken into account when using and developing aerosol models.

  6. Combined effects of organic aerosol loading and fog processing on organic aerosols oxidation, composition, and evolution.

    PubMed

    Chakraborty, Abhishek; Gupta, Tarun; Tripathi, S N

    2016-12-15

    Chemical characterization of ambient non-refractory submicron aerosols (NR-PM1) was carried out in real time at Kanpur, India. The measurements were performed during the winter (December 2014 to February 2015), and comprised of two very distinct high and low aerosol loading periods coupled with prevalent foggy conditions. The average non-refractory submicron aerosol loading varied significantly from high (HL, ~240μg/m(3)) to low loading (LL, ~100μg/m(3)) period and was dominated by organic aerosols (OA) which contributed more than half (~60%) of the measured aerosol mass. OA source apportionment via positive matrix factorization (PMF) showed drastic changes in the composition of OA from HL to LL period. Overall, O/C (oxygen to carbon) ratios also varied significantly from HL (=0.59) to LL (=0.69) period. Fog episodes (n=17) studied here seem to be reducing the magnitude of the negative impact of OA loading on O/C ratio (OA loading and O/C ratio are anti-correlated, as higher OA loading allows gas to particle partitioning of relatively less oxidized organics) by 60% via aqueous processing. This study provided new insights into the combined effects of OA loading and fog aqueous processing on the evolution of ambient organic aerosols (OA) for the first time.

  7. Effect of Dust and Anthropogenic Aerosols on Columnar Aerosol Optical Properties over Darjeeling (2200 m asl), Eastern Himalayas, India

    PubMed Central

    Chatterjee, Abhijit; Ghosh, Sanjay K.; Adak, Anandamay; Singh, Ajay K.; Devara, Panuganti C. S.; Raha, Sibaji

    2012-01-01

    Background The loading of atmospheric particulate matter (aerosol) in the eastern Himalaya is mainly regulated by the locally generated anthropogenic aerosols from the biomass burning and by the aerosols transported from the distance sources. These different types of aerosol loading not only affect the aerosol chemistry but also produce consequent signature on the radiative properties of aerosol. Methodology/Principal Findings An extensive study has been made to study the seasonal variations in aerosol components of fine and coarse mode aerosols and black carbon along with the simultaneous measurements of aerosol optical depth on clear sky days over Darjeeling, a high altitude station (2200 masl) at eastern Himalayas during the year 2008. We observed a heavy loading of fine mode dust component (Ca2+) during pre-monsoon (Apr – May) which was higher by 162% than its annual mean whereas during winter (Dec – Feb), the loading of anthropogenic aerosol components mainly from biomass burning (fine mode SO42− and black carbon) were higher (76% for black carbon and 96% for fine mode SO42−) from their annual means. These high increases in dust aerosols during pre-monsoon and anthropogenic aerosols during winter enhanced the aerosol optical depth by 25 and 40%, respectively. We observed that for every 1% increase in anthropogenic aerosols, AOD increased by 0.55% during winter whereas for every 1% increase in dust aerosols, AOD increased by 0.46% during pre-monsoon. Conclusion/Significance The natural dust transport process (during pre-monsoon) plays as important a role in the radiation effects as the anthropogenic biomass burning (during winter) and their differential effects (rate of increase of the AOD with that of the aerosol concentration) are also very similar. This should be taken into account in proper modeling of the atmospheric environment over eastern Himalayas. PMID:22792264

  8. 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.

  9. The effect of sea ice loss on sea salt aerosol concentrations and the radiative balance in the Arctic

    NASA Astrophysics Data System (ADS)

    Struthers, H.; Ekman, A. M. L.; Glantz, P.; Iversen, T.; Kirkevåg, A.; Mårtensson, E. M.; Seland, Ø.; Nilsson, E. D.

    2011-04-01

    Understanding Arctic climate change requires knowledge of both the external and the local drivers of Arctic climate as well as local feedbacks within the system. An Arctic feedback mechanism relating changes in sea ice extent to an alteration of the emission of sea salt aerosol and the consequent change in radiative balance is examined. A set of idealized climate model simulations were performed to quantify the radiative effects of changes in sea salt aerosol emissions induced by prescribed changes in sea ice extent. The model was forced using sea ice concentrations consistent with present day conditions and projections of sea ice extent for 2100. Sea salt aerosol emissions increase in response to a decrease in sea ice, the model results showing an annual average increase in number emission over the polar cap (70-90° N) of 86 × 106 m-2 s-1 (mass emission increase of 23 μg m-2 s-1). This in turn leads to an increase in the natural aerosol optical depth of approximately 23%. In response to changes in aerosol optical depth, the natural component of the aerosol direct forcing over the Arctic polar cap is estimated to be between -0.2 and -0.4 W m-2 for the summer months, which results in a negative feedback on the system. The model predicts that the change in first indirect aerosol effect (cloud albedo effect) is approximately a factor of ten greater than the change in direct aerosol forcing although this result is highly uncertain due to the crude representation of Arctic clouds and aerosol-cloud interactions in the model. This study shows that both the natural aerosol direct and first indirect effects are strongly dependent on the surface albedo, highlighting the strong coupling between sea ice, aerosols, Arctic clouds and their radiative effects.

  10. Analyzing the Contribution of Aerosols to an Observed Increase in Direct Normal Irradiance in Oregon

    SciTech Connect

    Riihimaki, Laura D.; Vignola, F.; Long, Charles N.

    2009-01-22

    Annual average total irradiance increases by 1-2% per decade at three mon- itoring stations in Oregon over the period from 1980 to 2007. Direct normal irradiance measurements increase by 5% per decade over the same time pe- riod. The measurements show no sign of a dimming before 1990. The impact of high concentrations of stratospheric aerosols following the volcanic erup- tions of El Chich¶on and Mt. Pinatubo are clearly seen in the measurements. Removing these years from the annual average all-sky time series reduces the trends in both total and direct normal irradiance. Clear-sky periods from this long direct normal time series are used in conjunction with radiative trans- fer calculations to test whether part of the increase could be caused by an- thropogenic aerosols. All three sites show relatively low clear-sky measure- ments before the eruption of El Chich¶on in 1982, suggesting higher aerosol loads during this period. After removing the periods most strongly impacted by volcanic eruptions, two of the sites show statistically signi¯cant increases in clear-sky direct normal irradiance from 1987 to 2007. Radiative transfer calculations of the impact of volcanic aerosols and tropospheric water vapor indicate that only about 20% of that clear-sky increase between background aerosol periods before and after the eruption of Mt. Pinatubo can be explained by these two factors. Thus, a statistically signi¯cant clear-sky trend remains between 1987 and 2007 that is consistent with the hypothesis that at least some of the increase in surface irradiance could be caused by a reduction of anthropogenic aerosols. D

  11. 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

    levels of atmospheric pollutants or intense biomass burning events in the region. However, numerous mineral dust plumes were observed during the campaign, with the main sources located in Morocco, Algeria and Tunisia, leading to aerosol optical depth (AOD) values ranging between 0.2 and 0.6 (at 440 nm) over the western and central Mediterranean basins. One important point of this experiment concerns the direct observations of aerosol extinction onboard the ATR-42, using the CAPS system, showing local maxima reaching up to 150 M m-1 within the dust plume. Non-negligible aerosol extinction (about 50 M m-1) has also been observed within the marine boundary layer (MBL). By combining the ATR-42 extinction coefficient observations with absorption and scattering measurements, we performed a complete optical closure revealing excellent agreement with estimated optical properties. This additional information on extinction properties has allowed calculation of the dust single scattering albedo (SSA) with a high level of confidence over the western Mediterranean. Our results show a moderate variability from 0.90 to 1.00 (at 530 nm) for all flights studied compared to that reported in the literature on this optical parameter. Our results underline also a relatively low difference in SSA with values derived near dust sources. In parallel, active remote-sensing observations from the surface and onboard the F-20 aircraft suggest a complex vertical structure of particles and distinct aerosol layers with sea spray and pollution located within the MBL, and mineral dust and/or aged North American smoke particles located above (up to 6-7 km in altitude). Aircraft and balloon-borne observations allow one to investigate the vertical structure of the aerosol size distribution showing particles characterized by a large size (> 10 µm in diameter) within dust plumes. In most of cases, a coarse mode characterized by an effective diameter ranging between 5 and 10 µm, has been detected above the

  12. 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

  13. Reallocation in modal aerosol models: impacts on predicting aerosol radiative effects

    NASA Astrophysics Data System (ADS)

    Korhola, T.; Kokkola, H.; Korhonen, H.; Partanen, A.-I.; Laaksonen, A.; Lehtinen, K. E. J.; Romakkaniemi, S.

    2013-08-01

    In atmospheric modelling applications the aerosol particle size distribution is commonly represented by modal approach, in which particles in different size ranges are described with log-normal modes within predetermined size ranges. Such method includes numerical reallocation of particles from a mode to another for example during particle growth, leading to potentially artificial changes in the aerosol size distribution. In this study we analysed how this reallocation affects climatologically relevant parameters: cloud droplet number concentration, aerosol-cloud interaction coefficient and light extinction coefficient. We compared these parameters between a modal model with and without reallocation routines, and a high resolution sectional model that was considered as a reference model. We analysed the relative differences of the parameters in different experiments that were designed to cover a wide range of dynamic aerosol processes occurring in the atmosphere. According to our results, limiting the allowed size ranges of the modes and the following numerical remapping of the distribution by reallocation, leads on average to underestimation of cloud droplet number concentration (up to 100%) and overestimation of light extinction (up to 20%). The analysis of aerosol first indirect effect is more complicated as the ACI parameter can be either over- or underestimated by the reallocating model, depending on the conditions. However, for example in the case of atmospheric new particle formation events followed by rapid particle growth, the reallocation can cause around average 10% overestimation of the ACI parameter. Thus it is shown that the reallocation affects the ability of a model to estimate aerosol climate effects accurately, and this should be taken into account when using and developing aerosol models.

  14. Effect of relative humidity on mixed aerosols in atmosphere.

    PubMed

    Lee, W M; Huang, W M; Chen, Y Y

    2001-01-01

    In this study, the effects of relative humidity on the deliquescent point and size of internally mixed aerosols diameter, NH4NO3 and (NH4)2SO4 were investigated using a Tandem Differential Mobility Analyzer (TDMA) with a relative humidity conditioner. The growth of mixed aerosols appears to have two deliquescent steps. The first one was at about 61.2-61.3%, but the second one was at around 77-78%. At the first deliquescence point, growth ratio at phase change was 7.5%, which agrees with the growth ratio of ammonium nitrate aerosol. Growth ratio of phase change at the second deliquescence point was about 20%, lower than the growth ratio of ammonium sulfate aerosol. In the relative humidity range of 80-85%, the growth ratio of the mixed aerosols reached 60%. In other words, it appears that growth ratio increases with the size of aerosol. Furthermore, a theoretical growth model of mixed aerosols was developed and applied to estimate the amount of composition of the mixed aerosols dissolved at each deliquescence point. The results also show that some of ammonium sulfate already dissolved at the first deliquescence point according to the theoretical growth model.

  15. Effects of Aerosols over the Indian Ocean

    NASA Technical Reports Server (NTRS)

    2002-01-01

    Aerosols that contain black carbon both absorb and reflect incoming sunlight. Even as these atmospheric particles reduce the amount of sunlight reaching the surface, they increase the amount of solar energy absorbed in the atmosphere, thus making it possible to both cool the surface and warm the atmosphere. The images above show satellite measurements of the region studied during the Indian Ocean Experiment (INDOEX)a vast region spanning the Arabian Sea and Bay of Bengal (west to east), and from the foot of the Himalayan Mountains, across the Indian subcontinent to the southern Indian Ocean (north to south). The Aerosol images show aerosol pollution (brownish pixels) in the lower atmosphere over the INDOEX study area, as measured by the Moderate-resolution Imaging Spectroradiometer (MODIS) aboard Terra. These were composited from March 14-21, 2001. The Albedo images show the total solar energy reflected back to space, as measured by Clouds and Earth's Radiant Energy System (CERES) aboard Terra. White pixels show high values, greens are intermediate values, and blues are low. Note how the aerosols, particularly over the ocean, increase the amount of energy reflected back to space. The Atmospheric Warming images show the absorption of the black carbon aerosols in the atmosphere. Where the aerosols are most dense, the absorption is highest. Red pixels indicate the highest levels of absorption, blues are low. The Surface Cooling images show that the aerosol particles reduce the amount of sunlight reaching the surface. Dark pixels show where the aerosols exert their cooling influence on the surface (or a high magnitude of negative radiative forcing). The bright pixels show where there is much less aerosol pollution and the incoming sunlight is relatively unaffected.

  16. Radiative effects of interannually varying vs. interannually invariant aerosol emissions from fires

    DOE PAGES

    Grandey, Benjamin S.; Lee, Hsiang-He; Wang, Chien

    2016-11-23

    Open-burning fires play an important role in the earth's climate system. In addition to contributing a substantial fraction of global emissions of carbon dioxide, they are a major source of atmospheric aerosols containing organic carbon, black carbon, and sulfate. These “fire aerosols” can influence the climate via direct and indirect radiative effects. In this study, we investigate these radiative effects and the hydrological fast response using the Community Atmosphere Model version 5 (CAM5). Emissions of fire aerosols exert a global mean net radiative effect of −1.0 W m−2, dominated by the cloud shortwave response to organic carbon aerosol. The net radiative effect ismore » particularly strong over boreal regions. Conventionally, many climate modelling studies have used an interannually invariant monthly climatology of emissions of fire aerosols. However, by comparing simulations using interannually varying emissions vs. interannually invariant emissions, we find that ignoring the interannual variability of the emissions can lead to systematic overestimation of the strength of the net radiative effect of the fire aerosols. Globally, the overestimation is +23 % (−0.2 W m−2). Regionally, the overestimation can be substantially larger. For example, over Australia and New Zealand the overestimation is +58 % (−1.2 W m−2), while over Boreal Asia the overestimation is +43 % (−1.9 W m−2). The systematic overestimation of the net radiative effect of the fire aerosols is likely due to the non-linear influence of aerosols on clouds. However, ignoring interannual variability in the emissions does not appear to significantly impact the hydrological fast response. In order to improve understanding of the climate system, we need to take into account the interannual variability of aerosol emissions.« less

  17. Profiling Transboundary Aerosols over Taiwan and Assessing Their Radiative Effects

    NASA Technical Reports Server (NTRS)

    Wang, Sheng-Hsiang; Lin, Neng-Huei; Chou, Ming-Dah; Tsay, Si-Chee; Welton, Ellsworth J.; Hsu, N. Christina; Giles, David M.; Liu, Gin-Rong; Holben, Brent N.

    2010-01-01

    A synergistic process was developed to study the vertical distributions of aerosol optical properties and their effects on solar heating using data retrieved from ground-based radiation measurements and radiative transfer simulations. Continuous MPLNET and AERONET observations were made at a rural site in northern Taiwan from 2005 to 2007. The aerosol vertical extinction profiles retrieved from ground-based lidar measurements were categorized into near-surface, mixed, and two-layer transport types, representing 76% of all cases. Fine-mode (Angstrom exponent, alpha, approx.1.4) and moderate-absorbing aerosols (columnar single-scattering albedo approx.0.93, asymmetry factor approx.0.73 at 440 nm wavelength) dominated in this region. The column-integrated aerosol optical thickness at 500 nm (tau(sub 500nm)) ranges from 0.1 to 0.6 for the near-surface transport type, but can be doubled in the presence of upper-layer aerosol transport. We utilize aerosol radiative efficiency (ARE; the impact on solar radiation per unit change of tau(sub 500nm)) to quantify the radiative effects due to different vertical distributions of aerosols. Our results show that the ARE at the top-of-atmosphere (-23 W/ sq m) is weakly sensitive to aerosol vertical distributions confined in the lower troposphere. On the other hand, values of the ARE at the surface are -44.3, -40.6 and -39.7 W/sq m 38 for near-surface, mixed, and two-layer transport types, respectively. Further analyses show that the impact of aerosols on the vertical profile of solar heating is larger for the near-surface transport type than that of two-layer transport type. The impacts of aerosol on the surface radiation and the solar heating profiles have implications for the stability and convection in the lower troposphere.

  18. Spectral aerosol direct radiative forcing from airborne radiative measurements during CalNex and ARCTAS

    NASA Astrophysics Data System (ADS)

    Leblanc, Samuel E.; Schmidt, K. S.; Pilewskie, P.; Redemann, J.; Hostetler, C.; Ferrare, R.; Hair, J.; Langridge, J. M.; Lack, D. A.

    2012-09-01

    This study presents the aerosol radiative forcing derived from airborne measurements of shortwave spectral irradiance during the 2010 Research at the Nexus of Air Quality and Climate Change (CalNex). Relative forcing efficiency, the radiative forcing normalized by aerosol optical thickness and incident irradiance, is a means of comparing the aerosol radiative forcing for different conditions. In this study, it is used to put the aerosol radiative effects of an air mass in the Los Angeles basin in context with case studies from three field missions that targeted other regions and aerosol types, including a case study from the Arctic Research of the Composition of the Troposphere from Aircraft and Satellites (ARCTAS). For CalNex, we relied on irradiance measurements onboard the NOAA P-3 aircraft during a flight on 19 May 2010 over a ground station. CalNex presented a difficulty for determining forcing efficiency since one of the input parameters, optical thickness, was not available from the same aircraft. However, extinction profiles were available from a nearby aircraft. An existing retrieval algorithm was modified to use those measurements as initial estimate for the missing optical thickness. In addition, single scattering albedo and asymmetry parameter (secondary products of the method), were compared with CalNex in situ measurements. The CalNex relative forcing efficiency spectra agreed with earlier studies that found this parameter to be constrained at each wavelength within 20% per unit of aerosol optical thickness at 500 nm regardless of aerosol type and experiment, except for highly absorbing aerosols sampled near Mexico City. The diurnally averaged below-layer forcing efficiency integrated over the wavelength range of 350-700 nm for CalNex is estimated to be -58.6 ± 13.8 W/m2, whereas for the ARCTAS case it is -48.7 ± 11.5 W/m2.

  19. A climatologically significant aerosol longwave indirect effect in the Arctic

    NASA Astrophysics Data System (ADS)

    Lubin, Dan; Vogelmann, Andrew M.

    2006-01-01

    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 3.4watts 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.

  20. Cyclosporin a aerosol improves the anticancer effect of Paclitaxel aerosol in mice.

    PubMed Central

    Knight, Vernon; Koshkina, N. V.; Golunski, E.; Roberts, L. E.; Gilbert, B. E.

    2004-01-01

    Paclitaxel (PTX) is a lipophilic agent with broad anticancer activity. In the present study we examined the antitumor effect and toxicity of co-administration of cyclosporine A (CsA) and PTX in liposomal aerosol using the Renca lung metastases mouse model. The untreated and PTX-only groups exhibited cancer growth while CsA aerosol plus PTX had more favorable effects on tumor growth. Weight loss was seen in mice treated with CsA/PTX+CsA by day 9 to 22. Histopathological examination showed no toxicity following treatment. The findings offer evidence that a combination of CsA and PTX may be suitable for aerosol treatment of lung cancer if it is possible to control toxicity of the therapy. Images Fig. 1 PMID:17060982

  1. Effect of CALIPSO Cloud Aerosol Discrimination (CAD) Confidence Levels on Observations of Aerosol Properties near Clouds

    NASA Technical Reports Server (NTRS)

    Yang, Weidong; Marshak, Alexander; Varnai, Tamas; Liu, Zhaoyan

    2012-01-01

    CALIPSO aerosol backscatter enhancement in the transition zone between clouds and clear sky areas is revisited with particular attention to effects of data selection based on the confidence level of cloud-aerosol discrimination (CAD). The results show that backscatter behavior in the transition zone strongly depends on the CAD confidence level. Higher confidence level data has a flatter backscatter far away from clouds and a much sharper increase near clouds (within 4 km), thus a smaller transition zone. For high confidence level data it is shown that the overall backscatter enhancement is more pronounced for small clear-air segments and horizontally larger clouds. The results suggest that data selection based on CAD reduces the possible effects of cloud contamination when studying aerosol properties in the vicinity of clouds.

  2. 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

  3. Spatially resolved measurements of size and velocity distributions of aerosol droplets from a direct injection nebulizer

    SciTech Connect

    Shum, S.C.K.; Johnson, S.K.; Pang, H.M.; Houk, R.S. )

    1993-05-01

    Aerosol droplet sizes and velocities from a direct injection nebulizer (DIN) are measured with radial and axial spatial resolution by phase Doppler particle analysis (PDPA). The droplets on the central axis of the spray become finer and their size becomes more uniform when [approx]20% methanol is added to the usual aqueous solvent. This could explain why the analyte signal is a maximum at this solvent composition when the DIN is used for inductively coupled plasma-mass spectrometry (ICP-MS). Mean droplet velocities are 12 to 22 m s[sup [minus]1] with standard deviations of [plus minus]4 to [plus minus]7 m s[sup [minus]1]. The outer fringes of the aerosol plume tend to be enriched in large droplets. The Sauter mean diameter (D[sub 3,2]) and velocity of the droplets also vary substantially with axial position in the aerosol plume. 35 refs., 10 figs., 1 tab.

  4. Real Effect or Artifact of Cloud Cover on Aerosol Optical Thickness?

    SciTech Connect

    Jeong, M-J.; Li, Z.

    2005-03-18

    retrievals of AOT from both satellite and ground sensors; (2) separate artifact from real effect; (3) create ''clean'' aerosol products for studying their direct and indirect effect. Presented are some very preliminary findings.

  5. 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.

  6. Aerosol effects on climate in China: a consistent picture?

    NASA Astrophysics Data System (ADS)

    Folini, Doris; Wild, Martin

    2013-04-01

    Population growth and industrialization in China in recent decades were accompanied by a substantial increase in aerosol emissions. Corresponding inventory data as well as consequences of increasing aerosol emissions are debated on the quantitative level, e.g. urbanization effects in observed data. We use transient sensitivity studies with the global atmosphere only climate model ECHAM5-HAM (aerosol emission data from NIES, the National Institute of Environmental Studies, Japan; prescribed, observation based sea surface temperatures (SSTs) from the Hadley Center) to investigate the effect of different aerosol emissions on surface solar radiation (SSR), surface air temperature (SAT), and precipitation. Observed and modeled SSR show a decrease of around -7 W/m2 in eastern parts of China, before increasing again in the late 1990s. Modeled SAT reflects the decrease in SSR in recent decades but carries also a substantial SST signature, in particular in the first half of the 20th century. Modeled precipitation decreases under the influence of increasing aerosol emissions, the 'northern drought, southern flood' pattern gets lost. We discuss how modeled changes due to increasing aerosol emissions compare with observations and what this may imply for the prescribed aerosol emissions, the model results, and the observed data.

  7. Laser Propagation Experiments - Aerosol and Stagnation Zone Effects

    DTIC Science & Technology

    1977-08-01

    Phys. 46, 402 (1975). 5. D. E. Lencioni and H. Kleiman. Effects of Aerosol Particle Heating on Laser Beam Propagation, Project Report LTP -27 on...1977. 18. J. Herrmann and L. C. Bradley. Numerical Calculations of Light Propagat , MIT/Lincln Laboratory Laser Technology Program Report LTP -10...R77-922578-13 ,/ Laser Propagation Experimets Aerosol and Stagnation "Zone Effects Final Technical Report "June 19, 1977 M.C. Fowe; J.R. Dunphy 3.3 0

  8. Direct aerosol chemical composition measurements to evaluate the physicochemical differences between controlled sea spray aerosol generation schemes

    NASA Astrophysics Data System (ADS)

    Collins, D. B.; Zhao, D. F.; Ruppel, M. J.; Laskina, O.; Grandquist, J. R.; Modini, R. L.; Stokes, M. D.; Russell, L. M.; Bertram, T. H.; Grassian, V. H.; Deane, G. B.; Prather, K. A.

    2014-07-01

    Controlled laboratory studies of the physical and chemical properties of sea spray aerosol (SSA) must be underpinned by a physically and chemically accurate representation of the bubble mediated production of nascent SSA particles. Since bubble bursting is sensitive to the physicochemical properties of seawater, any important differences in the SSA production mechanism are projected into SSA composition. Using direct chemical measurements of SSA at the single-particle level, this study presents an inter-comparison of three laboratory-based, bubble-mediated SSA production schemes: gas forced through submerged sintered glass filters ("frits"), a pulsed plunging waterfall apparatus, and breaking waves in a wave channel filled with natural seawater. The size-resolved chemical composition of SSA particles produced by breaking waves is more similar to particles produced by the plunging waterfall than sintered glass filters. Aerosol generated by disintegrating foam produced by sintered glass filters contained a larger fraction of organic enriched particles and a different size-resolved elemental composition, especially in the 0.8-2 μm size range. These particles, when dried, had more spherical morphologies compared to the more cubic structure expected for pure NaCl particles, which can be attributed to the presence of additional organic carbon. In addition to an inter-comparison of three SSA production methods, the role of the episodic or "pulsed" nature of the waterfall method utilized in this study on SSA composition was undertaken. In organic-enriched seawater, the continuous operation of the plunging waterfall mechanism resulted in the accumulation of surface foam and an over-expression of organic matter in SSA particles compared to pulsed plunging waterfall. Throughout this set of experiments, comparative differences in the SSA number size distribution were coincident with differences in aerosol composition, indicating that the production mechanism of SSA exerts

  9. 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

    . Nevertheless, the strengths of the statistical relationships are good predictors for the aerosol forcings in the models. An estimate of the total short-wave aerosol forcing inferred from the combination of these predictors for the modelled forcings with the satellite-derived statistical relationships yields a global annual mean value of -1.5+-0.5 Wm-2. An alternative estimate obtained by scaling the simulated clear- and cloudy-sky forcings with estimates of anthropogenic Ta and satellite-retrieved Nd - Ta regression slopes, respectively, yields a global annual mean clear-sky (aerosol direct effect) estimate of -0.4+-0.2 Wm-2 and a cloudy-sky (aerosol indirect effect) estimate of -0.7+-0.5 Wm-2, with a total estimate of -1.2+-0.4 Wm-2.

  10. Effects of meteoric debris on stratospheric aerosols and gases

    NASA Technical Reports Server (NTRS)

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

    1981-01-01

    Characterizations of meteoric dust height and size distributions are obtained using Hunten's calculations of meteor ablation and recondensation rates. The contribution of meteor residues to aerosol composition, the role of meteoric dust as condensation nuclei, and the effects of meteor debris on aerosol size distributions are quantified, and particle surface areas are estimated. The potential importance of heterogeneous chemistry for stratospheric trace gases is discussed. The interaction between H2SO4 vapor and meteor metal vapors is investigated. It is concluded that meteoric particles may dominate the natural stratospheric aerosols at small (less than .01 micron radius) and large (greater than 1 micron radius) sizes under normal conditions.

  11. Indirect aerosol effect increases CMIP5 models projected Arctic warming

    SciTech Connect

    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 aerosol 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.

  12. Aerosol indirect effect on tropospheric ozone via lightning

    NASA Astrophysics Data System (ADS)

    Yuan, T.; Remer, L. A.; Bian, H.; Ziemke, J. R.; Albrecht, R. I.; Pickering, K. E.; Oreopoulos, L.; Goodman, S. J.; Yu, H.; Allen, D. J.

    2012-12-01

    Tropospheric ozone (O3) is a pollutant and major greenhouse gas and its radiative forcing is still uncertain. The unresolved difference between modeled and observed natural background O3 concentrations is a key source of the uncertainty. Here we demonstrate remarkable sensitivity of lightning activity to aerosol loading with lightning activity increasing more than 30 times per unit of aerosol optical depth over our study area. 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 suggest O3 is increased as a result of aerosol-induced increase in lightning and lightning produced NOx. Model simulations with prescribed lightning change corroborate the satellite data analysis. This aerosol-O3 connection is achieved via aerosol increasing lightning and thus lightning produced nitrogen oxides. This aerosol-lightning-ozone link provides a potential physical mechanism that may account for a part of the model-observation difference in background O3 concentration. More importantly, O3 production increase from this link is concentrated in the upper troposphere, where O3 is most efficient as a greenhouse gas. Both of these implications suggest a stronger O3 historical radiative forcing. This introduces a new pathway, through which increasing in aerosols from pre-industrial time to present day enhances tropospheric O3 production. Aerosol forcing thus has a warming component via its effect on O3 production. Sensitivity simulations suggest that 4-8% increase of 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

  13. 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).

  14. Effects of Aircraft On Aerosol Abundance in the Upper Troposphere

    NASA Technical Reports Server (NTRS)

    Ferry, G. V.; Pueschel, R. F.; Strawa, A. W.; Howard, S. D.; Verma, S.; Mahoney, M. J.; Bui, T. P.; Hannan, J. R.; Fuelberg, H. E.; Condon, Estelle P. (Technical Monitor)

    1999-01-01

    A significant increase in sulfuric acid aerosol concentration was detected above 10 km pressure altitude during a cross-corridor flight out of Shannon on October 23, 1997. The source of this aerosol is ascribed to commercial aircraft operations in flight corridors above 10 km, because (1) a stable atmosphere prevented vertical air mass exchanges and thus eliminated surface sources, (2) air mass back trajectories documented the absence of remote continental sources, and (3) temperature profiler data showed the tropopause at least one kilometers above flight altitude throughout the flight. Particle volatility identified 70% H2SO4, 20% (NH4)2SO4 and 10% nonvolatile aerosol in the proximity of flight corridors, and (10-30)% H2SO4, up to 50% (NH4)2SO4, and (40-60)% nonvolatile aerosols in air that was not affected by aircraft operations below 10 km. Only a very small fraction of the nonvolatile particles (determined with a condensation nucleus counter) could be morphologically identified as soot aerosol (validated by scanning electron microscopy of wire impactor samples). The newly formed H2SO4 particles did not measurably affect surface area and volume of the background aerosol due to their small size, hence did not affect radiative transfer directly.

  15. Effects of aerosols on tropospheric oxidants: A global model study

    NASA Astrophysics Data System (ADS)

    Tie, Xuexi; Brasseur, Guy; Emmons, Louisa; Horowitz, Larry; Kinnison, Douglas

    2001-10-01

    The global distributions of sulfate and soot particles in the atmosphere are calculated, and the effect of aerosol particles on tropospheric oxidants is studied using a global chemical/transport/aerosol model. The model is developed in the framework of the National Center for Atmospheric Research (NCAR) global three-dimensional chemical/transport model (Model for Ozone and Related Chemical Tracers (MOZART)). In addition to the gas-phase photochemistry implemented in the MOZART model, the present study also accounts for the formation of sulfate and black carbon aerosols as well as for heterogeneous reactions on particles. The simulated global sulfate aerosol distributions and seasonal variation are compared with observations. The seasonal variation of sulfate aerosols is in agreement with measurements, except in the Arctic region. The calculated vertical profiles of sulfate aerosol agree well with the observations over North America. In the case of black carbon the calculated surface distribution is in fair agreement with observations. The effects of aerosol formation and heterogeneous reactions on the surface of sulfate aerosols are studied. The model calculations show the following: (1) The concentration of H2O2 is reduced when sulfate aerosols are formed due to the reaction of SO2 + H2O2 in cloud droplets. The gas-phase reaction SO2 + OH converts OH to HO2, but the reduction of OH and enhancement of HO2 are insignificant (<3%). (2) The heterogeneous reaction of HO2 on the surface of sulfate aerosols produces up to 10% reduction of hydroperoxyl radical (HO2) with an uptake coefficient of 0.2. However, this uptake coefficient could be overestimated, and the results should be regard as an upper limit estimation. (3) The N2O5 reaction on the surface of sulfate aerosols leads to an 80% reduction of NOx at middle to high latitudes during winter. Because ozone production efficiency is low in winter, ozone decreases by only 10% as a result of this reaction. However

  16. 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.

    2014-08-01

    Aerosol particles were characterized by an Aerodyne Aerosol Chemical Speciation Monitor (ACSM) along with various collocated instruments in Beijing, China to investigate the aerosol composition and sources during the Chinese Spring Festival, 2013. Three fireworks (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 showed major impacts on non-refractory potassium, chloride, sulfate, and organics in PM1, of which the FW organics appeared to be mainly secondary with its mass spectrum resembling to 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 PM1 accounting for 63-82% during the nine PEs observed. The elevated contributions of secondary species during PEs resulted in a higher mass extinction efficiency of PM1 (6.4 m2 g-1) than that during CPs (4.4 m2 g-1). The Chinese Spring Festival also provides a unique opportunity to study the impacts of reduced anthropogenic emissions on aerosol chemistry in the city. The primary species showed ubiquitous reductions during the holiday period with the largest reduction for cooking OA (69%), nitrogen monoxide (54%), and coal combustion OA (28%). The secondary sulfate, however, remained minor change, and the SOA and the total PM2.5 even slightly increased. These results have significant implications that controlling local primary source emissions, e.g., cooking and traffic activities, might have limited effects on improving air quality during PEs when SPM that is formed over regional scales dominates aerosol particle composition.

  17. Aerosol-radiation-cloud interactions in a regional coupled model: the effects of convective parameterisation and resolution

    NASA Astrophysics Data System (ADS)

    Archer-Nicholls, Scott; Lowe, Douglas; Schultz, David M.; McFiggans, Gordon

    2016-05-01

    The Weather Research and Forecasting model with Chemistry (WRF-Chem) has been used to simulate a region of Brazil heavily influenced by biomass burning. Nested simulations were run at 5 and 1 km horizontal grid spacing for three case studies in September 2012. Simulations were run with and without fire emissions, convective parameterisation on the 5 km domain, and aerosol-radiation interactions in order to explore the differences attributable to the parameterisations and to better understand the aerosol direct effects and cloud responses. Direct aerosol-radiation interactions due to biomass burning aerosol resulted in a net cooling, with an average short-wave direct effect of -4.08 ± 1.53 Wm-2. However, around 21.7 Wm-2 is absorbed by aerosol in the atmospheric column, warming the atmosphere at the aerosol layer height, stabilising the column, inhibiting convection, and reducing cloud cover and precipitation. The changes to clouds due to radiatively absorbing aerosol (traditionally known as the semi-direct effects) increase the net short-wave radiation reaching the surface by reducing cloud cover, producing a secondary warming that counters the direct cooling. However, the magnitude of the semi-direct effect was found to be extremely sensitive to the model resolution and the use of convective parameterisation. Precipitation became organised in isolated convective cells when not using a convective parameterisation on the 5 km domain, reducing both total cloud cover and total precipitation. The SW semi-direct effect varied from 6.06 ± 1.46 with convective parameterisation to 3.61 ± 0.86 Wm-2 without. Convective cells within the 1 km domain are typically smaller but with greater updraft velocity than equivalent cells in the 5 km domain, reducing the proportion of the domain covered by cloud in all scenarios and producing a smaller semi-direct effect. Biomass burning (BB) aerosol particles acted as cloud condensation nuclei (CCN), increasing the droplet number

  18. Direct radiative forcing properties of atmospheric aerosols over semi-arid region, Anantapur in India.

    PubMed

    Kalluri, Raja Obul Reddy; Gugamsetty, Balakrishnaiah; Kotalo, Rama Gopal; Nagireddy, Siva Kumar Reddy; Tandule, Chakradhar Rao; Thotli, Lokeswara Reddy; Rajuru Ramakrishna, Reddy; Surendranair, Suresh Babu

    2016-10-01

    This paper describes the aerosols optical, physical characteristics and the aerosol radiative forcing pertaining to semi-arid region, Anantapur for the period January 2013-December 2014. Collocated measurements of Aerosol Optical Depth (AOD) and Black Carbon mass concentration (BC) are carried out by using MICROTOPS II and Aethalometer and estimated the aerosol radiative forcing over this location. The mean values of AOD at 500nm are found to be 0.47±0.09, 0.34±0.08, 0.29±0.06 and 0.30±0.07 during summer, winter, monsoon and post-monsoon respectively. The Angstrom exponent (α380-1020) value is observed maximum in March (1.25±0.19) and which indicates the predominance of fine - mode aerosols and lowest in the month of July (0.33±0.14) and may be due to the dominance of coarse-mode aerosols. The diurnal variation of BC is exhibited two height peaks during morning 07:00-08:00 (IST) and evening 19:00-21:00 (IST) hours and one minima noticed during afternoon (13:00-16:00). The highest monthly mean BC concentration is observed in the month of January (3.4±1.2μgm(-3)) and the lowest in July (1.1±0.2μgm(-3)). The estimated Aerosol Direct Radiative Forcing (ADRF) in the atmosphere is found to be +36.8±1.7Wm(-2), +26.9±0.2Wm(-2), +18.0±0.6Wm(-2) and +18.5±3.1Wm(-2) during summer, winter, monsoon and post-monsoon seasons, respectively. Large difference between TOA and BOA forcing is observed during summer which indicate the large absorption of radiant energy (36.80Wm(-2)) which contributes more increase in atmospheric heating by ~1K/day. The BC contribution on an average is found to be 64% and is responsible for aerosol atmospheric heating.

  19. Downward solar global irradiance at the surface in São Paulo city - The climatological effects of aerosol and clouds

    NASA Astrophysics Data System (ADS)

    Yamasoe, M. A.; Rosário, N. M. E.; Barros, K. M.

    2017-01-01

    We analyzed the variability of downward solar irradiance reaching the surface at São Paulo city, Brazil, and estimated the climatological aerosol and cloud radiative effects. Eleven years of irradiance were analyzed, from 2005 to 2015. To distinguish the aerosol from the cloud effect, the radiative transfer code LibRadtran was used to calculate downward solar irradiance. Two runs were performed, one considering only ozone and water vapor daily variability, with AOD set to zero and the second allowing the three variables to change, according to mean climatological values. The difference of the 24 h mean irradiance calculated with and without aerosol resulted in the shortwave aerosol direct radiative effect, while the difference between the measured and calculated, including the aerosol, represented the cloud effect. Results showed that, climatologically, clouds can be 4 times more effective than aerosols. The cloud shortwave radiative effect presented a maximum reduction of about -170 W m-2 in January and a minimum in July, of -37 W m-2. The aerosol direct radiative effect was maximum in spring, when the transport of smoke from the Amazon and central parts of South America is frequent toward São Paulo. Around mid-September, the 24 h radiative effect due to aerosol only was estimated to be -50 W m-2. Throughout the rest of the year, the mean aerosol effect was around -20 W m-2 and was attributed to local urban sources. The effect of the cloud fraction on the cloud modification factor, defined as the ratio of all-sky irradiation to cloudless sky irradiation, showed dependence on the cloud height. Low clouds presented the highest impact while the presence of high clouds only almost did not affect solar transmittance, even in overcast conditions.

  20. 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; Kristansson, Jon Egill; Liu, Xiaohong; Balkanski, Yves; Donner, Leo J.; Ginoux, Paul A.; Stier, Philip; Grandey, Benjamin; 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

    2010-03-12

    strongly influenced by the simulated anthropogenic fraction of {tau}{sub a}, and parameterization assumptions such as a lower bound on N{sub d}. Nevertheless, the strengths of the statistical relationships are good predictors for the aerosol forcings in the models. An estimate of the total short-wave aerosol forcing inferred from the combination of these predictors for the modelled forcings with the satellite-derived statistical relationships yields a global annual mean value of -1.5 {+-} 0.5 Wm{sup -2}. In an alternative approach, the radiative flux perturbation due to anthropogenic aerosols can be broken down into a component over the cloud-free portion of the globe (approximately the aerosol direct effect) and a component over the cloudy portion of the globe (approximately the aerosol indirect effect). An estimate obtained by scaling these simulated clear- and cloudy-sky forcings with estimates of anthropogenic {tau}{sub a} and satellite-retrieved Nd - {tau}{sub a} regression slopes, respectively, yields a global, annual-mean aerosol direct effect estimate of -0.4 {+-} 0.2 Wm{sup -2} and a cloudy-sky (aerosol indirect effect) estimate of -0.7 {+-} 0.5 Wm{sup -2}, with a total estimate of -1.2 {+-} 0.4 Wm{sup -2}.

  1. Total reflection X-ray fluorescence (TXRF) for direct analysis of aerosol particle samples.

    PubMed

    Bontempi, E; Zacco, A; Benedetti, D; Borgese, L; Colombi, P; Stosnach, H; Finzi, G; Apostoli, P; Buttini, P; Depero, L E

    2010-04-14

    Atmospheric aerosol particles have a great impact on the environment and on human health. Routine analysis of the particles usually involves only the mass determination. However, chemical composition and phases provide fundamental information about the particles' origins and can help to prevent health risks. For example, these particles may contain heavy metals such as Pb, Ni and Cd, which can adversely affect human health. In this work, filter samples were collected in Brescia, an industrial town located in Northern Italy. In order to identify the chemical composition and the phases of the atmospheric aerosols, the samples were analysed by means of total reflection X-ray fluorescence (TXRF) spectrometry with a laboratory instrument and X-ray microdiffraction at Synchrotron Daresbury Laboratories, Warrington (Cheshire, UK). The results are discussed and correlated to identify possible pollution sources. The novelty of this analytical approach is that filter samples for TXRF were analysed directly and did not require chemical pretreatment to leach elements from the aerosol particulates. The results of this study clearly show that TXRF is a powerful technique for the analysis of atmospheric aerosols on 'as-received' filters, thereby leaving samples intact and unaltered for possible subsequent analyses by other methods. In addition, the low detection limits for many elements (low ng/cm2) indicate that this method may hold promise in various application fields, such as nanotechnology.

  2. 3D direct impacts of urban aerosols on dynamics during the CAPITOUL field experiment

    NASA Astrophysics Data System (ADS)

    Aouizerats, B.; Tulet, P.; Gomes, L.

    2012-12-01

    Evaluating the radiative impacts of aerosol particles is of great interest for understanding atmospheric physics and processes feedbacks. To respond to such objectives, the online fully coupled model Meso-NH is applied to a real case during a two-day Intensive Observation Period (IOP) of the CAPITOUL campaign. The aerosol optical properties are computed from the chemical composition and the size distribution of the particle population, and are compared to observations and analysed at local and regional scales. The differences between two simulations are then studied in order to isolate the direct radiative impacts of aerosols on dynamics. Results show that the aerosol particles generate a forcing on shortwave flux by a decrease of the amount reaching the surface up to 30 Wm-2. The resulting feedbacks lead to a cooling up to 0.6 K on the 2-meter temperature over the city of Toulouse and over the larger 125 km by 125 km area around Toulouse. This cooling is also modeled along the whole boundary layer, leading to a decrease of the boundary layer height up to -50 m during the afternoon and a decrease of the vertical velocities with an average of -3 %.

  3. 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

  4. Evidence for a Glaciation Aerosol Indirect Effect from Ship Tracks

    NASA Astrophysics Data System (ADS)

    Christensen, M.; Suzuki, K.; Stephens, G. L.

    2013-12-01

    Ship tracks are a prominent manifestation of the aerosol indirect effect that provides a unique opportunity to study aerosol interactions in both warm and mixed-phase clouds. While ample evidence supports that an increase in aerosol concentration generally suppresses warm phase precipitation leading to longer cloud lifetime and more reflected sunlight (Albrecht, 1989) there is less understood about these effects in mixed-phase clouds. Lohmann, (2002) propose that an increase in IN (Ice Nuclei) may cause a glaciation indirect effect which results in more frequent glaciation of super-cooled droplets via the Bergeron process thereby increasing the amount of precipitation, which could decrease cloud cover, cloud longevity, and reflected sunlight. In this study, over 200 ship tracks are identified in mixed phase clouds using MODIS (MODerate resolution Imaging Spectroradiometer) imagery. Retrievals of the ice phase are obtained using CALIPSO (Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observations). These measurements provide evidence that glaciation is more frequent in polluted clouds compared to the unpolluted clouds that lie adjacent to ship tracks. Larger ice fractions may result from the increased IN emitted from the ship or by other processes (e.g., immersion/contact freezing) that lead to faster ice multiplication in polluted clouds with smaller and more numerous supercooled droplets. Observations from the profiling radar on CloudSat show that aerosol suppresses warm phase precipitation but enhances the cold phase precipitation. For mixed-phase clouds, these differences roughly cancel resulting in small changes in precipitation between polluted and unpolluted clouds. When cloud tops are warm, aerosol decreases precipitation rates and cloud water paths due to the entrainment effect but the differences in cloud water amount are considerably smaller than those found in cold phase clouds. These results provide the first glance of ship tracks in mixed

  5. UV spectral irradiance measurements in New Zealand: Effects of Pinatubo volcanic aerosol

    NASA Technical Reports Server (NTRS)

    Mckenzie, Richard L.

    1994-01-01

    Since late 1989, regular UV spectral irradiance measurements have been made at Lauder, New Zealand (45 deg S, 170 deg E), whenever weather permits. Here, the instrumentation and measurement strategy are outlined, and early results are discussed. Following the eruption of Mt Pinatubo in June 1991, large amounts of volcanic aerosol were injected into the stratosphere and were subsequently transported to New Zealand's latitudes in the latter half of 1991. This provides an opportunity to investigate the effects of volcanic aerosols on UV irradiances measured at this clean-air site. Although changes in global (sum of diffuse plus direct) irradiances were below the detection threshold, there were significant changes in the partitioning of radiation between the direct beam and diffuse skylight. Decreases by nearly a factor of two in the direct/diffuse ratio were observed at longer wavelengths, and at smaller solar zenith angles (sza's). The aerosol optical depth due to volcanic aerosol over Lauder in December 1991 was 0.15 plus or minus 0.02 at 450 nm, with lower values at shorter wavelengths. Although effects were relatively small in the UVB region, an implication of the changes is that the contrast between shade and direct sun is reduced, so that shaded areas received relatively more radiation in the summer of 1991/92 in New Zealand.

  6. 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

  7. A numerical study of aerosol effects on electrification of thunderstorms

    NASA Astrophysics Data System (ADS)

    Tan, Y. B.; Shi, Z.; Chen, Z. L.; Peng, L.; Yang, Y.; Guo, X. F.; Chen, H. R.

    2017-02-01

    Numerical simulations are performed to investigate the effect of aerosol on microphysical and electrification in thunderstorm clouds. A two-dimensional (2-D) cumulus model with electrification scheme including non-inductive and inductive charge separation is used. The concentration of aerosol particles with distribution fitted by superimposing three log-normal distributions rises from 50 to 10,000 cm-3. The results show that the response of charge separation rate to the increase of aerosol concentration is nonmonotonic. When aerosol concentration is changed from 50 to 1000 cm-3, a stronger formation of cloud droplet, graupel and ice crystal results in increasing charge separation via non-inductive and inductive mechanism. However, in the range of 1000-3000 cm-3, vapor competition arises in the decrease of ice crystal mixing ratio and the reduction of ice crystals size leads to a slightly decrease in non-inductive charge rate, while inductive charging rate has no significant change in magnitude. Above aerosol concentration of 3000 cm-3, the magnitude of charging rate which keeps steady is insensitive to the increase in aerosol concentration. The results also suggest that non-inductive charge separation between ice crystal and graupel contributes to the main upper positive charge region and the middle negative charge region. Inductive graupel-cloud droplet charge separation, on the other hand, is found to play an important role in the development of lower charge region.

  8. Using Aerocom Results to Constrain Black Carbon, Sulphate and Total Direct Aerosol Radiative Forcing and Their Uncertainties

    NASA Astrophysics Data System (ADS)

    Samset, B. H.; Myhre, G.

    2014-12-01

    Aerosols affect the global radiative balance, and hence the climate, through a multitude of processes. However, even the direct interaction of aerosols with incoming sunlight is at present insufficiently constrained. Here we compare the output of 15 recent aerosol climate models (AeroCom Phase II), both column averaged and vertically resolved. Through a simple MonteCarlo approach, we show that the model based total anthropogenic aerosol direct radiative forcing (DRF) uncertainty may be underestimated. Constraining modelled vertical profiles of black carbon (BC) concentration to aircraft measurements in remote regions, we further show that recent BC DRF estimates may be biased high. A short modelled BC lifetime is indicated as a necessary, though not sufficient, requirement for reproducing measurements. Finally, modeled sulphate aerosol DRF is discussed in the context of differences in representation of humidity and hygroscopic growth in the models.

  9. Effects of biomass burning aerosols on CO2 fluxes on Amazon Region

    NASA Astrophysics Data System (ADS)

    Soares Moreira, Demerval; Freitas, Saulo; Longo, Karla; Rosario, Nilton

    2015-04-01

    During the dry season in Central Brazil and Southern Amazon, there is an usually high concentration of aerosol particles associated with intense human activities, with extensive biomass burning. It has been observed through remote sensing that the smoke clouds in these areas often cover an area of about 4 to 5 million km2. Thus, the average aerosol optical depth of these regions at 500 ηm, is usually below 0.1 during the rainy season and can exceed 0.9 in the fire season. Aerosol particles act as condensation nuclei and also increase scattering and absorption of the incident radiation. Therefore, the layer of the aerosol alters the precipitation rate; reduces the amount of solar energy that reaches the surface, producing a cooling; and causes an increase of diffuse radiation. These factors directly and indirectly affect the CO2 fluxes at the surface. In this work, the chemical-atmospheric model CCATT-BRAMS (Coupled Chemistry-Aerosol-Tracer Transport model to the Brazilian developments on the Regional Atmospheric Modeling System) coupled to the surface model JULES (Joint UK Land Environment Simulator) was used to simulate the effects of biomass burning aerosols in CO2 fluxes in the Amazon region. Both the total effect of the aerosols and the contribution related only to the increase of the diffuse fraction caused by the their presence were analyzed. The results show that the effect of the scattered fraction is dominant over all other effects. It was also noted that the presence of aerosols from fires can substantially change biophysiological processes of the carbon cycle. In some situations, it can lead to a sign change in the net ecosystem exchange (NEE), turning it from a source of CO2 to the atmosphere, when the aerosol is not considered in the simulations, to a sink, when it is considered. Thus, this work demonstrates the importance of considering the presence of aerosols in numerical simulations of weather and climate, since carbon dioxide is a major

  10. Effects of Biomass Burning Aerosols on CO2 Fluxes in the Amazon Region

    NASA Astrophysics Data System (ADS)

    Moreira, D. S.; Freitas, S. R.

    2014-12-01

    During the dry season in Central Brazil and Southern Amazon, there is an usually high concentration of aerosol particles associated with intense human activities, with extensive biomass burning. It has been observed through remote sensing that the smoke clouds in these areas often cover an area of about 4 to 5 million km2. Thus, the average aerosol optical depth of these regions at 500 ηm, is usually below 0.1 during the rainy season and can exceed 0.9 in the fire season. Aerosol particles act as condensation nuclei and also increase scattering and absorption of the incident radiation. Therefore, the layer of the aerosol alters the precipitation rate; reduces the amount of solar energy that reaches the surface, producing a cooling; and causes an increase of diffuse radiation. These factors directly and indirectly affect the CO2 fluxes at the surface. In this work, the chemical-atmospheric model CCATT-BRAMS (Coupled Chemistry-Aerosol-Tracer Transport model to the Brazilian developments on the Regional Atmospheric Modeling System) coupled to the surface model JULES (Joint UK Land Environment Simulator) was used to simulate the effects of biomass burning aerosols in CO2 fluxes in the Amazon region. Both the total effect of the aerosols and the contribution related only to the increase of the diffuse fraction caused by the their presence were analyzed. The results show that the effect of the scattered fraction is dominant over all other effects. It was also noted that the presence of aerosols from fires can substantially change biophysiological processes of the carbon cycle. In some situations, it can lead to a sign change in the net ecosystem exchange (NEE), turning it from a source of CO2 to the atmosphere, when the aerosol is not considered in the simulations, to a sink, when it is considered. Thus, this work demonstrates the importance of considering the presence of aerosols in numerical simulations of weather and climate, since carbon dioxide is a major

  11. Indirect aerosol effect increases CMIP5 models projected Arctic warming

    DOE PAGES

    Chylek, Petr; Vogelsang, Timothy J.; Klett, James D.; ...

    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

  12. Method for estimating the atmospheric content of sub-micrometer aerosol using direct-sun photometric data

    NASA Astrophysics Data System (ADS)

    Stefan, S.; Filip, L.

    2009-04-01

    It is well known that the aerosol generated by human activity falls in the sub-micrometer rage [1]. The rapid increase of such emissions led to massive accumulations in the planetary boundary layer. Aerosol pollutants influence the quality of life on the Earth in at least two ways: by direct physiological effects following their penetration into living organisms and by the indirect implications on the overall energy balance of the Earth-atmosphere system. For these reasons monitoring the sub-micrometer aerosol on a global scale, become a stringent necessity in protecting the environment. The sun-photometry proved a very efficient way for such monitoring activities, mainly when vast networks of instruments (like AERONET [2]) are used. The size distribution of aerosols is currently a product of AERONET obtained through an inversion algorithm of sky-photometry data [3, 4]. Alternatively, various methods of investigating the aerosol size distribution have been developed through the use of direct-sun photometric data, with the advantages of simpler computation algorithms and a more convenient use [5, 6]. Our research aims to formulate a new simpler way to retrieve aerosol fine and coarse mode volume concentrations, as well as dimensional information, from direct-sun data. As in other works from the literature [3-6], the main hypothesis is that of a bi-modal shape of the size distribution of aerosols that can be reproduced rather satisfactorily by a linear combination of two lognormal functions. Essentially, the method followed in this paper relies on aerosol size information retrieval through fitting theoretical computations to measured aerosol optical depth (AOD) and related data. To this purpose, the experimental spectral dependence of AOD is interpolated and differentiated numerically to obtain the Ǻngström parameter. The reduced (i.e. normalized to the corresponding columnar volumetric content) contributions of the fine and coarse modes to the AOD have also been

  13. The Effect of Non-Lambertian Surface Reflectance on Aerosol Radiative Forcing

    SciTech Connect

    Ricchiazzi, P.; O'Hirok, W.; Gautier, C.

    2005-03-18

    Surface reflectance is an important factor in determining the strength of aerosol radiative forcing. Previous studies of radiative forcing assumed that the reflected surface radiance is isotropic and does not depend on incident illumination angle. This Lambertian reflection model is not a very good descriptor of reflectance from real land and ocean surfaces. In this study we present computational results for the seasonal average of short and long wave aerosol radiative forcing at the top of the atmosphere and at the surface. The effect of the Lambertian assumption is found through comparison with calculations using a more detailed bi-direction reflectance distribution function (BRDF).

  14. Webinar Presentation: Linking Regional Aerosol Emission Changes with Multiple Impact Measures through Direct and Cloud-Related Forcing Estimates

    EPA Pesticide Factsheets

    This presentation, Linking Regional Aerosol Emission Changes with Multiple Impact Measures through Direct and Cloud-Related Forcing Estimates, was given at the STAR Black Carbon 2016 Webinar Series: Accounting for Impact, Emissions, and Uncertainty.

  15. Evaluation of atmospheric aerosol and tropospheric ozone effects on global terrestrial ecosystem carbon dynamics

    NASA Astrophysics Data System (ADS)

    Chen, Min

    The increasing human activities have produced large amounts of air pollutants ejected into the atmosphere, in which atmospheric aerosols and tropospheric ozone are considered to be especially important because of their negative impacts on human health and their impacts on global climate through either their direct radiative effect or indirect effect on land-atmosphere CO2 exchange. This dissertation dedicates to quantifying and evaluating the aerosol and tropospheric ozone effects on global terrestrial ecosystem dynamics using a modeling approach. An ecosystem model, the integrated Terrestrial Ecosystem Model (iTem), is developed to simulate biophysical and biogeochemical processes in terrestrial ecosystems. A two-broad-band atmospheric radiative transfer model together with the Moderate-Resolution Imaging Spectroradiometer (MODIS) measured atmospheric parameters are used to well estimate global downward solar radiation and the direct and diffuse components in comparison with observations. The atmospheric radiative transfer modeling framework were used to quantify the aerosol direct radiative effect, showing that aerosol loadings cause 18.7 and 12.8 W m -2 decrease of direct-beam Photosynthetic Active Radiation (PAR) and Near Infrared Radiation (NIR) respectively, and 5.2 and 4.4 W m -2 increase of diffuse PAR and NIR, respectively, leading to a total 21.9 W m-2 decrease of total downward solar radiation over the global land surface during the period of 2003-2010. The results also suggested that the aerosol effect may be overwhelmed by clouds because of the stronger extinction and scattering ability of clouds. Applications of the iTem with solar radiation data and with or without considering the aerosol loadings shows that aerosol loading enhances the terrestrial productions [Gross Primary Production (GPP), Net Primary Production (NPP) and Net Ecosystem Production (NEP)] and carbon emissions through plant respiration (RA) in global terrestrial ecosystems over the

  16. Susceptibility of Tribolium confusum (Coleoptera: Tenebrionidae) to pyrethrin aerosol: effects of aerosol particle size, concentration, and exposure conditions

    Technology Transfer Automated Retrieval System (TEKTRAN)

    A series of laboratory studies were conducted to assess effect of droplet size on efficacy of pyrethrin aerosol against adults of Tribolium confusum Jacqueline DuVal, the confused flour beetle. A vertical flow aerosol exposure chamber that generated a standardized particle size diameter was used for...

  17. Aerosol-radiation-cloud interactions in a regional coupled model: the effects of convective parameterisation and resolution

    NASA Astrophysics Data System (ADS)

    Archer-Nicholls, S.; Lowe, D.; Schultz, D. M.; McFiggans, G.

    2015-10-01

    The Weather Research and Forecasting model with Chemistry (WRF-Chem) has been used to simulate a region of Brazil heavily influenced by biomass burning. Nested simulations were run at 5 km and 1 km horizontal grid spacing for three case studies in September 2012. Simulations were run with and without fire emissions, convective parameterisation on the 5 km domain and aerosol-radiation interactions in order to explore the differences attributable to the parameterisations and to better understand the aerosol direct effects and cloud responses. Direct aerosol-radiation interactions due to biomass burning aerosol resulted in a net cooling, with an average reduction of downwelling shortwave radiation at the surface of -24.7 W m-2 over the three case studies. However, around 21.7 W m-2 is absorbed by aerosol in the atmospheric column, warming the atmosphere at the aerosol layer height, stabilising the column, inhibiting convection and reducing cloud cover and precipitation. The changes to clouds due to radiatively interacting aerosol (traditionally known as the semi-direct effects) increase net shortwave radiation reaching the surface by reducing cloud cover, producing a secondary warming that largely counters the direct cooling. However, the magnitude of the semi-direct effect was difficult to quantify, being extremely sensitive to the model resolution and use of convective parameterisation. The 1 km domain simulated clouds less horizontally spread, reducing the proportion of the domain covered by cloud in all scenarios and producing a smaller semi-direct effect. Not having a convective parameterisation on the 5 km domain reduced total cloud cover, but also total precipitation. BB aerosol particles acted as CCN, increasing the droplet number concentration of clouds. However, the changes to cloud properties had negligible impact on net radiative balance on either domain, with or without convective parameterisation. Sensitivity to the uncertainties relating to the semi-direct

  18. Determination of Aerosol Optical Depth and Land Surface Directional Reflectances Using Multiangle Imagery

    NASA Technical Reports Server (NTRS)

    Martonchik, John V.

    1997-01-01

    Spectral aerosol optical depths, surface hemispherical-directional reflectance factors, and bihemispherical reflectances (albedos) are retrieved for an area of Glacier National Park using spectral, multiangle imagery obtained with the airborne advanced solid state array spectroradiometer (ASAS). The retrieval algorithms are described and are identical in principle to those being devised for use by the multiangle imaging spectroradiometer (MISR) which will fly on the EOS-AMI spacecraft in 1998. As part of its science mission, MISR will produce global coverage of both aerosol amounts an an surface reflection properties. The results in this paper represent the initial effort in applying the MISR algorithms to real data. These algorithms will undergo additional testing and validation as more multiangle data become available.

  19. A new high spectral resolution lidar technique for direct retrievals of cloud and aerosol extinction

    NASA Astrophysics Data System (ADS)

    Yorks, J. E.; McGill, M. J.; Hlavka, D. L.

    2014-12-01

    The Airborne Cloud-Aerosol Transport System (ACATS) is a Doppler lidar system and high spectral resolution lidar (HSRL) recently developed at NASA Goddard Space Flight Center (GSFC). ACATS passes the returned atmospheric backscatter through a single etalon and divides the transmitted signal into several channels (wavelength intervals), which are measured simultaneously and independently (Figure 1). Both the particulate and molecular scattered signal can be directly and unambiguously measured, allowing for direct retrievals of particle extinction. The broad Rayleigh-scattered spectrum is imaged as a nearly flat background, illustrated in Figure 1c. The integral of the particulate backscattered spectrum is analogous to the aerosol measurement from the typical absorption filter HSRL technique in that the molecular and particulate backscatter components can be separated (Figure 1c and 1d). The main difference between HSRL systems that use the iodine filter technique and the multichannel etalon technique used in the ACATS instrument is that the latter directly measures the spectral broadening of the particulate backscatter using the etalon to filter out all backscattered light with the exception of a narrow wavelength interval (1.5 picometers for ACATS) that contains the particulate spectrum (grey, Figure 1a). This study outlines the method and retrieval algorithms for ACATS data products, focusing on the HSRL derived cloud and aerosol properties. While previous ground-based multi-channel etalon systems have been built and operated for wind retrievals, there has been no airborne demonstration of the technique and the method has not been used to derive HSRL cloud and aerosol properties. ACATS has flown on the NASA ER-2 during flights over Alaska in July 2014 and as part of the Wallops Airborne Vegetation Experiment (WAVE) in September 2012. This study will focus on the HSRL aspect of the ACATS instrument, since the method and retrieval algorithms have direct application

  20. Effects of ozone and aerosol on surface UV radiation variability.

    PubMed

    Kim, Jhoon; Cho, Hi-Ku; Mok, Jungbin; Yoo, Hee Dong; Cho, Nayeong

    2013-02-05

    Global (direct+diffuse) spectral ultraviolet (UV, 290-363nm) and total ozone measurements made on the roof of the Main Science Building, Yonsei University at Seoul (37.57°, 128.98°E) were analyzed to quantify the effects of ozone and aerosol on the variability of surface erythemal UV (EUV) irradiance. The measurements have been made with a Brewer Spectrophotometer MKIV (SCI-TEC#148) and a Dobson Ozone Spectrophotometer (Beck#123), respectively, during 2004-2008. The overall mean radiation amplification factor, RAF(AOD, SZA) [23,24] due to total ozone (O(3)) (hereafter O(3) RAF) shows that 1% decrease in total ozone results in an increase of 1.18±0.02% in the EUV irradiance with the range of 0.67-1.74% depending on solar zenith angles (SZAs) (40-70°) and on aerosol optical depths (AODs) (<4.0), under both clear (cloud cover<25%) and all sky conditions. For the mean AOD, the O(3) RAFs(SZA) for both sky conditions increased as SZA increased from 40° to 60°, and then decreased for higher SZA 70°, where the patterns are consistent with results of the previous studies [2,10]. A similar analysis of the RAF(O(3), SZA) due to AOD (hereafter AOD RAF) under clear and all-sky conditions shows that on average, a 1% increase in AOD forces a decrease of 0.29±0.06% in the EUV irradiance with the maximum range 0.18-0.63% depending on SZAs and O(3). Thus, overall sensitivity of UV to ozone (O(3), RAF) was estimated to be about four times higher than to the aerosol (AOD RAF). At the mean O(3), the AOD RAFs(SZA) for both skies appears to be almost independent of SZAs. It is shown that the O(3) RAFs are nearly independent of the sky conditions, whereas the AOD RAFs depend distinctly on the sky conditions with the larger values for all skies. Under cloud free conditions, the overall mean ratio for measured-to-modeled O(3), RAF(AOD, SZA) is 1.13, whereas the ratio for AOD RAF(O(3), SZA) shows 0.82 in the EUV irradiance. Overall, the RAF measurements are corroborated by radiative

  1. Effect of aerosol propellants and surfactants on airway resistance

    PubMed Central

    Sterling, G. M.; Batten, J. C.

    1969-01-01

    The effects on the airways of inhalation of the vehicles used in two commercial pressurized bronchodilator aerosols were studied in 20 normal and seven asthmatic subjects. Changes in bronchial calibre due to bronchoconstriction were measured as changes in airway resistance using a constant volume whole body plethysmograph, and results were expressed as changes in the ratio Airway conductance/Thoracic gas volume (=specific airway conductance). The aerosols caused very slight bronchoconstriction in the normal subjects, with a mean decrease of 5·3% in specific airway conductance after inhalation of a spray containing sorbitol trioleate as a surface tension lowering agent, and of 9·7% after inhalation of a spray containing lecithin. This effect was prevented by prior inhalation of atropine methonitrate, and its mechanism was therefore probably a vagally mediated reflex. The bronchoconstriction was also reversed by the addition of isoprenaline to the aerosol. The asthmatic subjects showed larger mean reductions in specific airway conductance of 13% and 21% after sorbitol and lecithin respectively: the response was again prevented by atropine. We conclude that, although the aerosol vehicles cause slight bronchoconstriction, this is unlikely to be a clinical danger since it is insufficient to cause symptoms of wheezing, and is less than that caused by inhalation of a single cigarette. Moreover, the constriction is regularly converted to dilatation in both normal and asthmatic subjects by the addition of atropine or isoprenaline to the aerosol. PMID:5821624

  2. Comparison of Aerosol Classification From Airborne High Spectral Resolution Lidar and the CALIPSO Vertical Feature Mask

    NASA Technical Reports Server (NTRS)

    Burton, Sharon P.; Ferrare, Rich A.; Omar, Ali H.; Vaughan, Mark A.; Rogers, Raymond R.; Hostetler, Chris a.; Hair, Johnathan W.; Obland, Michael D.; Butler, Carolyn F.; Cook, Anthony L.; Harper, David B.

    2012-01-01

    Knowledge of aerosol composition and vertical distribution is crucial for assessing the impact of aerosols on climate. In addition, aerosol classification is a key input to CALIOP aerosol retrievals, since CALIOP requires an inference of the lidar ratio in order to estimate the effects of aerosol extinction and backscattering. In contrast, the NASA airborne HSRL-1 directly measures both aerosol extinction and backscatter, and therefore the lidar ratio (extinction-to-backscatter ratio). Four aerosol intensive properties from HSRL-1 are combined to infer aerosol type. Aerosol classification results from HSRL-1 are used here to validate the CALIOP aerosol type inferences.

  3. A survey of effects of gaseous and aerosol pollutants on pulmonary function of normal males.

    PubMed

    Stacy, R W; Seal, E; House, D E; Green, J; Roger, L J; Raggio, L

    1983-01-01

    A total of 231 normal male human subjects were exposed for 4 hr to air, ozone, nitrogen dioxide, or sulfur dioxide; to sulfuric acid, ammonium bisulfate, ammonium sulfate, or ammonium nitrate aerosols; or to mixtures of these gaseous and aerosol pollutants. Only one concentration of each pollutant was used. This study, therefore, represents a preliminary survey, intended to allow direct comparison of studies to plan future research. During exposure each subject had two 15-min exercise sessions on a treadmill at 4 mph and 10% grade. Environmental conditions were mildly stressful, i.e., temperature = 30 degrees C and relative humidity = 60%. A battery of 19 measurements of pulmonary function was performed just prior to exposure (air control); 2 hr into the exposure, following the first exercise session; 4 hr into the exposure, following the second exercise session; and 24 hr after exposure. Significant differences were noted in specific airway resistance (SRAW), forced vital capacity (FVC), and forced expiratory flow at 50% of FVC (FEF50) and in related measurements in those experimental groups exposed to ozone or to ozone plus aerosols. None of the aerosols alone, nitrogen dioxide or sulfur dioxide alone, or mixtures of nitrogen dioxide or sulfur dioxide with aerosols produced significant effects. A distribution analysis of subject responsivity to ozone gave a normal distribution among subjects not exposed to ozone, and a distribution shifted to the right and skewed to the right among those exposed to ozone alone or in mixture, with no evidence of bimodal distribution of ozone sensitivity.

  4. An effective inversion algorithm for retrieving bimodal aerosol particle size distribution from spectral extinction data

    NASA Astrophysics Data System (ADS)

    He, Zhenzong; Qi, Hong; Yao, Yuchen; Ruan, Liming

    2014-12-01

    The Ant Colony Optimization algorithm based on the probability density function (PDF-ACO) is applied to estimate the bimodal aerosol particle size distribution (PSD). The direct problem is solved by the modified Anomalous Diffraction Approximation (ADA, as an approximation for optically large and soft spheres, i.e., χ≫1 and |m-1|≪1) and the Beer-Lambert law. First, a popular bimodal aerosol PSD and three other bimodal PSDs are retrieved in the dependent model by the multi-wavelength extinction technique. All the results reveal that the PDF-ACO algorithm can be used as an effective technique to investigate the bimodal PSD. Then, the Johnson's SB (J-SB) function and the modified beta (M-β) function are employed as the general distribution function to retrieve the bimodal PSDs under the independent model. Finally, the J-SB and M-β functions are applied to recover actual measurement aerosol PSDs over Beijing and Shanghai obtained from the aerosol robotic network (AERONET). The numerical simulation and experimental results demonstrate that these two general functions, especially the J-SB function, can be used as a versatile distribution function to retrieve the bimodal aerosol PSD when no priori information about the PSD is available.

  5. Effect of volcanic aerosols on stratospheric radiance at wavelengths between 8 and 13 microm.

    PubMed

    Halperin, B; Murcray, D G

    1987-06-01

    A set of stratospheric aerosol optical models is employed in a radiative-transfer computation to study the effects of postvolcanic particle size distributions and compositions on the spectral radiance in the 8-13-microm window region. The models are based on direct measurements of post El Chichon aerosol size distributions and vertical profiles. They represent various maturity states of aerosols composed of sulfuric acid aqueous solutions, formed and evolved in the stratosphere following a massive volcanic eruption. Comparisons are made with concurrent radiance observations obtained on balloon flights 6 months after the eruption and 1 yr later. Most of the calculations are done using the LOWTRAN-6 code (either alone or combined with a multiple scattering calculation), revised so as to include the appropriate aerosol optical models. A better quantitative agreement is found between the calculated and observed spectral radiances when the aerosol loading is relatively high, indicating that additional minor radiance sources of a yet unresolved nature should be incorporated in the present version of the calculation.

  6. Multi-Decadal Change of Atmospheric Aerosols and their Effects on Surface Radiation

    NASA Technical Reports Server (NTRS)

    Chin, Mian

    2011-01-01

    We present an investigation on multi-decadal changes of atmospheric aerosols and their effects on surface radiation using a global chemistry transport model along with the near-term to long-term data records. We focus on a 28-year time period of satellite era from 1980 to 2007) during which a suite of aerosol data from satellite observations) ground-based measurements) and intensive field experiments have become available. We analyze the long-term global and regional aerosol trends and their relationship to the changes of aerosol and precursor emissions and assess the role aerosols play in the multi-decadal change of solar radiation reaching the surface (known as "dimming" or "brightening") at different regions of the world) including the major anthropogenic source regions (North America) Europe) Asia) that have been experiencing considerable changes of emissions) dust and biomass burning regions that have large interannual variabilities) downwind regions that are directly affected by the changes in the source area) and remote regions that are considered to representing "backgroundH conditions.

  7. Aerosol effects on the anvil characteristics of mesoscale convective systems

    NASA Astrophysics Data System (ADS)

    Saleeby, S. M.; Heever, S. C.; Marinescu, P. J.; Kreidenweis, S. M.; DeMott, P. J.

    2016-09-01

    Simulations of two mesoscale convective systems (MCSs) that occurred during the Midlatitude Continental Convective Clouds Experiment were performed to examine the impact of aerosol number concentration on the vertical distributions of liquid and ice condensate and the macrophysical, microphysical, and radiative properties of the cirrus-anvil cloud shield. Analyses indicate that for an increase in aerosol concentration from a clean continental to a highly polluted state, there was an increase in the rime collection rate of cloud water, which led to less lofted cloud water. Aerosol-induced trends in the cloud mixing ratio profiles were, however, nonmonotonic in the mixed phase region, such that a moderate increase in aerosol concentration produced the greatest reduction in cloud water. Generally, less lofted cloud water led to less anvil ice mixing ratio but more numerous, small ice crystals within the anvil. In spite of reduced anvil ice mixing ratio, the anvil clouds exhibited greater areal coverage, increased albedo, reduced cloud top cooling, and reduced net radiative flux, which led to an aerosol-induced warming (reduced cooling) effect in these squall lines.

  8. Cloud Scavenging Effects on Aerosol Radiative and Cloud-nucleating Properties - Final Technical Report

    SciTech Connect

    Ogren, John A.; Sheridan, Patrick S.; Andrews, Elisabeth

    2009-03-05

    The optical properties of aerosol particles are the controlling factors in determining direct aerosol radiative forcing. These optical properties depend on the chemical composition and size distribution of the aerosol particles, which can change due to various processes during the particles’ lifetime in the atmosphere. Over the course of this project we have studied how cloud processing of atmospheric aerosol changes the aerosol optical properties. A counterflow virtual impactor was used to separate cloud drops from interstitial aerosol and parallel aerosol systems were used to measure the optical properties of the interstitial and cloud-scavenged aerosol. Specifically, aerosol light scattering, back-scattering and absorption were measured and used to derive radiatively significant parameters such as aerosol single scattering albedo and backscatter fraction for cloud-scavenged and interstitial aerosol. This data allows us to demonstrate that the radiative properties of cloud-processed aerosol can be quite different than pre-cloud aerosol. These differences can be used to improve the parameterization of aerosol forcing in climate models.

  9. Direct observation of aqueous secondary organic aerosol from biomass-burning emissions

    NASA Astrophysics Data System (ADS)

    Gilardoni, Stefania; Massoli, Paola; Paglione, Marco; Giulianelli, Lara; Carbone, Claudio; Rinaldi, Matteo; Decesari, Stefano; Sandrini, Silvia; Costabile, Francesca; Gobbi, Gian Paolo; Chiara Pietrogrande, Maria; Visentin, Marco; Scotto, Fabiana; Fuzzi, Sandro; Facchini, Maria Cristina

    2016-09-01

    The mechanisms leading to the formation of secondary organic aerosol (SOA) are an important subject of ongoing research for both air quality and climate. Recent laboratory experiments suggest that reactions taking place in the atmospheric liquid phase represent a potentially significant source of SOA mass. Here, we report direct ambient observations of SOA mass formation from processing of biomass-burning emissions in the aqueous phase. Aqueous SOA (aqSOA) formation is observed both in fog water and in wet aerosol. The aqSOA from biomass burning contributes to the “brown” carbon (BrC) budget and exhibits light absorption wavelength dependence close to the upper bound of the values observed in laboratory experiments for fresh and processed biomass-burning emissions. We estimate that the aqSOA from residential wood combustion can account for up to 0.1-0.5 Tg of organic aerosol (OA) per y in Europe, equivalent to 4-20% of the total OA emissions. Our findings highlight the importance of aqSOA from anthropogenic emissions on air quality and climate.

  10. Direct observation of aqueous secondary organic aerosol from biomass-burning emissions

    PubMed Central

    Massoli, Paola; Paglione, Marco; Giulianelli, Lara; Carbone, Claudio; Rinaldi, Matteo; Decesari, Stefano; Sandrini, Silvia; Costabile, Francesca; Gobbi, Gian Paolo; Pietrogrande, Maria Chiara; Visentin, Marco; Scotto, Fabiana; Fuzzi, Sandro; Facchini, Maria Cristina

    2016-01-01

    The mechanisms leading to the formation of secondary organic aerosol (SOA) are an important subject of ongoing research for both air quality and climate. Recent laboratory experiments suggest that reactions taking place in the atmospheric liquid phase represent a potentially significant source of SOA mass. Here, we report direct ambient observations of SOA mass formation from processing of biomass-burning emissions in the aqueous phase. Aqueous SOA (aqSOA) formation is observed both in fog water and in wet aerosol. The aqSOA from biomass burning contributes to the “brown” carbon (BrC) budget and exhibits light absorption wavelength dependence close to the upper bound of the values observed in laboratory experiments for fresh and processed biomass-burning emissions. We estimate that the aqSOA from residential wood combustion can account for up to 0.1–0.5 Tg of organic aerosol (OA) per y in Europe, equivalent to 4–20% of the total OA emissions. Our findings highlight the importance of aqSOA from anthropogenic emissions on air quality and climate. PMID:27551086

  11. Direct effects protection

    NASA Technical Reports Server (NTRS)

    1977-01-01

    Protection of an aircraft and each of its various systems against the direct effects of lightning were analyzed. Components located in different sections of the aircraft were individually examined since they are likely to experience different degrees of susceptibility to lightning, and may be vulnerable to different components of the lightning flash. The basic steps to be followed in establishing lightning protection were presented by discussing the varieties of arc entry and current flow-through damage. The lightning-strike zones and lightning current environments are established, since environmental conditions in the zones are those under which specific protective measures must perform. Airworthiness regulations which apply to lightning protection are cited.

  12. [Effectiveness of individual units of aerosol therapy equipment].

    PubMed

    Smirnova, L A; Perel'mutr, A S

    1975-01-01

    Various methods of drug atomization and future prospects for their application in medical practice are considered. On the ground of a research into the influence produced by the administered doses and the density of the aerosol on the therapeutic activity the expediency of employing aerosol generators based upon pneumatic atomization by using the principle of ejecting an additional volume of air, as units yielding a substantial curative effect, is demonstrated. Data which bear proof to economic advantages of the units under review are given.

  13. Advances in Quantifying the Radiative Effects of Aerosol Particles on Climate from Airborne Field Studies

    NASA Astrophysics Data System (ADS)

    Pilewskie, P.; Schmidt, K. S.; Coddington, O.; Bergstrom, R.; Redemann, J.

    2007-12-01

    In the fourth assessment report of the Intergovernmental Panel on Climate Change, large uncertainties persist in estimates of climate forcing by aerosol particles. One contributor to this uncertainty is the poorly quantified vertical distribution of solar radiation absorbed by aerosol particles, from the regional to global scale. Another is the spectral and spatial variability of surface albedo, an effect that can dominate the top-of-atmosphere perturbations due to aerosol scattering and absorption, particularly over land. Over the past three years a number of intensive airborne field experiments (ICARTT, MILAGRO, GoMACCS) have contributed significantly to our understanding of the impact of pollution outflow from urban-industrial centers on radiative forcing, using spectrally resolved radiometric measurements and novel observationally-based methods to derive forcing efficiency and flux divergence. We present an overview of some of the most significant advances in direct radiative forcing realized by these studies, and recommendations on where the greatest challenges remain. In addition we present findings from these experiments on the influence of aerosol particles on cloud radiative properties, a potentially greater effect but even more uncertain than direct radiative forcing.

  14. 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...

  15. Detecting Aerosol Effect on Deep Precipitation Systems: A Modeling Study

    NASA Astrophysics Data System (ADS)

    Li, X.; Tao, W.; Khain, A.; Kummerow, C.; Simpson, J.

    2006-05-01

    Urban cities produce high concentrations of anthropogenic aerosols. These aerosols are generally hygroscopic and may serve as Cloud Condensation Nuclei (CCN). This study focuses on the aerosol indirect effect on the deep convective systems over the land. These deep convective systems contribute to the majority of the summer time rainfall and are important for local hydrological cycle and weather forecast. In a companion presentation (Tao et al.) in this session, the mechanisms of aerosol-cloud-precipitation interactions in deep convective systems are explored using cloud-resolving model simulations. Here these model results will be analyzed to provide guidance to the detection of the impact of aerosols as CCN on summer time, deep convections using the currently available observation methods. The two-dimensional Goddard Cumulus Ensemble (GCE) model with an explicit microphysical scheme has been used to simulate the aerosol effect on deep precipitation systems. This model simulates the size distributions of aerosol particles, as well as cloud, rain, ice crystals, snow, graupel, and hail explicitly. Two case studies are analyzed: a midlatitude summer time squall in Oklahoma, and a sea breeze convection in Florida. It is shown that increasing the CCN number concentration does not affect the rainfall structure and rain duration in these two cases. The total surface rainfall rate is reduced in the squall case, but remains essentially the same in the sea breeze case. For the long-lived squall system with a significant portion of the stratiform rain, the surface rainfall PDF (probability density function) distribution is more sensitive to the change of the initial CCN concentrations compared with the total surface rainfall. The possibility of detecting the aerosol indirect effect in deep precipitation systems from the space is also studied in this presentation. The hydrometeors fields from the GCE model simulations are used as inputs to a microwave radiative transfer model

  16. Improved retrieval of direct and diffuse downwelling surface shortwave flux in cloudless atmosphere using dynamic estimates of aerosol content and type: application to the LSA-SAF project

    NASA Astrophysics Data System (ADS)

    Ceamanos, X.; Carrer, D.; Roujean, J.-L.

    2014-08-01

    .9, 6.5, and 19.1% for global, direct, and diffuse DSSF with regard to the McClear algorithm). The main limitation of the proposed approach is its high sensitivity to the quality of the ECMWF aerosol inputs, which is proved to be sufficiently accurate for reanalyses but not for forecast data. Given the proximity of DSSF retrieval to the modeling of the atmospheric direct effect, SIRAMix is also able to quantify the direct radiative forcing at the surface due to a given atmospheric component (e.g., gases or aerosols).

  17. Modeling Aerosol Effects on Shallow Cumuli and Turbulent Activities Under Various Meteorological Conditions

    NASA Astrophysics Data System (ADS)

    Wang, H.; McFarquhar, G. M.

    2007-12-01

    To determine conditions over the Indian Ocean for which cloud fields are most susceptible to modification from aerosols and to study how turbulent activities and shallow cumuli vary for different meteorological scenarios, the National Center for Atmospheric Research Eulerian-semi-Lagrangian (EULAG) three-dimensional large-eddy simulation model was initialized using data collected during the Indian Ocean Experiment (INDOEX). Radiosonde data were used to construct 6 soundings encompassing the range of temperature and humidity observed in the trade-wind boundary layer. By then adding the characteristics (height, depth and strength) of either a typical transition layer (TL), a strong inversion layer (IL) or no stable layer a total of 18 meteorological scenarios were produced. Separate simulations were conducted using EULAG assuming pristine and polluted conditions (i.e., cloud droplet number concentrations, aerosol extinction profiles and single-scattering albedos) using INDOEX observations. For the range of meteorological conditions observed during INDOEX, sensitivity studies showed that the semi- direct effect always dominated indirect effects, producing a positive daytime mean net indirect forcing varying between 0.2 and 4.5 W m-2. The simulations showed that changes in the environmental relative humidity (RH) and the presence of the TL had critical impacts on the cloud properties, turbulence and lateral detrainment rates, and on how aerosols affect these quantities. The net indirect forcing was larger when the RH was higher and in the absence of any dry and stable layers. It was reduced to less than 1.2 W m-2 when the TL was present. The impact of the IL was dependent on convective strength which increases with increasing RH. In fact, changes in meteorological factors had larger impacts on the simulated cloud properties than did the presence of anthropogenic aerosols, indicating large uncertainties can be introduced when solely using observations of aerosols and

  18. Experimental Measurements of the Effects of Photo-chemical Oxidation on Aerosol Emissions in Aircraft Exhaust

    NASA Astrophysics Data System (ADS)

    Miracolo, M. A.; Presto, A. A.; Hennigan, C. J.; Nguyen, N.; Ranjan, M.; Reeder, A.; Lipsky, E.; Donahue, N. M.; Robinson, A. L.

    2009-12-01

    dominant. At low loads, photo-oxidation increased aerosol loadings in the chamber by a factor of fifty. We attribute this substantial secondary organic aerosol (SOA) production to oxidation of low-volatility organic vapors emitted under low loads. At higher loads, we see more modest secondary aerosol production from both organics and inorganics. Therefore secondary aerosol production can substantially exceed the direct aerosol emissions from aircraft. The results underscore the dramatic effects that photo-oxidation has on aerosol emissions from aircraft.

  19. Simulating Aerosol Indirect Effects with Improved Aerosol-Cloud- Precipitation Representations in a Coupled Regional Climate Model

    SciTech Connect

    Zhang, Yang; Leung, L. Ruby; Fan, Jiwen

    2016-04-27

    This is a collaborative project among North Carolina State University, Pacific Northwest National Laboratory, and Scripps Institution of Oceanography, University of California at San Diego to address the critical need for an accurate representation of aerosol indirect effect in climate and Earth system models. In this project, we propose to develop and improve parameterizations of aerosol-cloud-precipitation feedbacks in climate models and apply them to study the effect of aerosols and clouds on radiation and hydrologic cycle. Our overall objective is to develop, improve, and evaluate parameterizations to enable more accurate simulations of these feedbacks in high resolution regional and global climate models.

  20. Effect of Hydrophilic Organic Seed Aerosols on Secondary Organic Aerosol Formation from Ozonolysis of α-Pinene

    SciTech Connect

    Song, Chen; Zaveri, Rahul A.; Shilling, John E.; Alexander, M. L.; Newburn, Matthew K.

    2011-07-26

    Gas-particle partitioning theory is widely used in atmospheric models to predict organic aerosol loadings. This theory predicts that secondary organic aerosol (SOA) yield of an oxidized VOC product will increase as the mass loading of preexisting organic aerosol increases. In a previous study, we showed that the presence of model hydrophobic primary organic aerosol (POA) had no detectable effect on the secondary organic aerosol (SOA) yields from ozonolysis of {alpha}-pinene, suggesting that the condensing SOA compounds form a separate phase from the preexisting POA. However, non-polar, hydrophobic POA may gradually become polar and hydrophilic as it undergoes oxidative aging while POA formed from biomass burning is already somewhat polar and hydrophilic. In this study, we investigate the effects of model hydrophilic POA such as fulvic acid, adipic acid and citric acid on the gas-particle partitioning of SOA from {alpha}-pinene ozonolysis. The results show that only citric acid seed significantly enhances the absorption of {alpha}-pinene SOA into the particle-phase. The other two POA seed particles have negligible effect on the {alpha}-pinene SOA yields, suggesting that {alpha}-pinene SOA forms a well-mixed organic aerosol phase with citric acid while a separate phase with adipic acid and fulvic acid. This finding highlights the need to improve the thermodynamics treatment of organics in current aerosol models that simply lump all hydrophilic organic species into a single phase, thereby potentially introducing an erroneous sensitivity of SOA mass to emitted POA.

  1. The radiative effect of aerosols in the earth's atmosphere

    NASA Technical Reports Server (NTRS)

    Wang, W.-C.; Domoto, G. A.

    1974-01-01

    A modified two-flux approximation is employed to compute the transfer of radiation in a finite, inhomogeneous, turbid atmosphere. A perturbation technique is developed to allow the treatment of nongray gaseous absorption with multiple scattering. The perturbation method, which employs a backscatter factor as a parameter, can be used with anisotropic particle scattering as well as Rayleigh scattering. This method is used to study the effect of aerosols on radiative solar heating and infrared cooling as well as the radiative-convective temperature distribution in the earth's atmosphere. It is found that the effect of aerosols in the infrared cannot be neglected; while in the visible, the effect can be of the same order as that due to absorption by water vapor. For a high surface albedo (greater than 0.30) heating of the earth-atmosphere system results due to the presence of aerosols. The aerosols also reduce the amount of convection needed to maintain a stable atmosphere. For the case of a dense haze a temperature inversion is found to exist close to the ground.

  2. 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.

  3. On the effect of different aerosol types on surface solar radiation levels over the region of Eastern Mediterranean

    NASA Astrophysics Data System (ADS)

    Alexandri, Georgia; Georgoulias, Aristeidis K.; Kourtidis, Konstantinos; Meleti, Charikleia; Balis, Dimitris

    2014-05-01

    In this work, we examine the direct effect of different aerosol types on the surface solar radiation (SSR) levels in the region of Eastern Mediterranean. Simulations with the Santa Barbara DISORT Atmospheric Radiative Transfer (SBDART) model were performed using ground and satellite-based data as input. An IDL tool that "feeds" SBDART with the appropriate input data was developed allowing us to simulate SSR with a time step of 1 hour. Level-2 aerosol optical depth, cloud optical depth, cloud fraction, effective droplet radius, cloud top pressure, precipitable water and surface albedo data from MODIS, as well as ozone total column data from Earth Probe TOMS and OMI satellite sensors, coarse resolution cloud data from the ISCCP and single scattering albedo, asymmetry factor and Angström exponent sunphotometric data from the AERONET are used in our radiative transfer simulations. Simulations are performed over selected spots within Eastern Mediterranean for clear, liquid cloud and ice cloud covered skies and for different aerosol types (maritime, dust, anthropogenic, fine-mode natural). The optical properties of aerosols were determined using a combination of satellite, ground-based, model and reanalysis products. The aerosol direct radiative effect is defined as the difference between simulations done with and without the presence of aerosols. This research has been financed by EPAN II and PEP under the national action "Bilateral, multilateral and regional R&T cooperations" (AEROVIS Sino-Greek project).

  4. Aerosol properties and associated radiative effects over Cairo (Egypt)

    NASA Astrophysics Data System (ADS)

    El-Metwally, M.; Alfaro, S. C.; Wahab, M. M. Abdel; Favez, O.; Mohamed, Z.; Chatenet, B.

    2011-02-01

    Cairo is one of the largest megacities in the World and the particle load of its atmosphere is known to be particularly important. In this work we aim at assessing the temporal variability of the aerosol's characteristics and the magnitude of its impacts on the transfer of solar radiation. For this we use the level 2 quality assured products obtained by inversion of the instantaneous AERONET sunphotometer measurements performed in Cairo during the Cairo Aerosol CHaracterization Experiment (CACHE), which lasted from the end of October 2004 to the end of March 2006. The analysis of the temporal variation of the aerosol's optical depth (AOD) and spectral dependence suggests that the aerosol is generally a mixture of at least 3 main components differing in composition and size. This is confirmed by the detailed analysis of the monthly-averaged size distributions and associated optical properties (single scattering albedo and asymmetry parameter). The components of the aerosol are found to be 1) a highly absorbing background aerosol produced by daily activities (traffic, industry), 2) an additional, 'pollution' component produced by the burning of agricultural wastes in the Nile delta, and 3) a coarse desert dust component. In July, an enhancement of the accumulation mode is observed due to the atmospheric stability favoring its building up and possibly to secondary aerosols being produced by active photochemistry. More generally, the time variability of the aerosol's characteristics is due to the combined effects of meteorological factors and seasonal production processes. Because of the large values of the AOD achieved during the desert dust and biomass burning episodes, the instantaneous aerosol radiative forcing (RF) at both the top (TOA) and bottom (BOA) of the atmosphere is maximal during these events. For instance, during the desert dust storm of April 8, 2005 RF BOA, RF TOA, and the corresponding atmospheric heating rate peaked at - 161.7 W/m 2, - 65.8 W/m 2

  5. Aerosol Monitoring during Carbon Nanofiber Production: Mobile Direct-Reading Sampling

    PubMed Central

    Evans, Douglas E.; Ku, Bon Ki; Birch, M. Eileen; Dunn, Kevin H.

    2010-01-01

    Detailed investigations were conducted at a facility that manufactures and processes carbon nanofibers (CNFs). Presented research summarizes the direct-reading monitoring aspects of the study. A mobile aerosol sampling platform, equipped with an aerosol instrument array, was used to characterize emissions at different locations within the facility. Particle number, respirable mass, active surface area, and photoelectric response were monitored with a condensation particle counter (CPC), a photometer, a diffusion charger, and a photoelectric aerosol sensor, respectively. CO and CO2 were additionally monitored. Combined simultaneous monitoring of these metrics can be utilized to determine source and relative contribution of airborne particles (CNFs and others) within a workplace. Elevated particle number concentrations, up to 1.15 × 106 cm−3, were found within the facility but were not due to CNFs. Ultrafine particle emissions, released during thermal treatment of CNFs, were primarily responsible. In contrast, transient increases in respirable particle mass concentration, with a maximum of 1.1 mg m−3, were due to CNF release through uncontrolled transfer and bagging. Of the applied metrics, our findings suggest that particle mass was probably the most useful and practical metric for monitoring CNF emissions in this facility. Through chemical means, CNFs may be selectively distinguished from other workplace contaminants (Birch et al., in preparation), and for direct-reading monitoring applications, the photometer was found to provide a reasonable estimate of respirable CNF mass concentration. Particle size distribution measurements were conducted with an electrical low-pressure impactor and a fast particle size spectrometer. Results suggest that the dominant CNF mode by particle number lies between 200 and 250 nm for both aerodynamic and mobility equivalent diameters. Significant emissions of CO were also evident in this facility. Exposure control recommendations

  6. Aerosol monitoring during carbon nanofiber production: mobile direct-reading sampling.

    PubMed

    Evans, Douglas E; Ku, Bon Ki; Birch, M Eileen; Dunn, Kevin H

    2010-07-01

    Detailed investigations were conducted at a facility that manufactures and processes carbon nanofibers (CNFs). Presented research summarizes the direct-reading monitoring aspects of the study. A mobile aerosol sampling platform, equipped with an aerosol instrument array, was used to characterize emissions at different locations within the facility. Particle number, respirable mass, active surface area, and photoelectric response were monitored with a condensation particle counter (CPC), a photometer, a diffusion charger, and a photoelectric aerosol sensor, respectively. CO and CO(2) were additionally monitored. Combined simultaneous monitoring of these metrics can be utilized to determine source and relative contribution of airborne particles (CNFs and others) within a workplace. Elevated particle number concentrations, up to 1.15 x 10(6) cm(-3), were found within the facility but were not due to CNFs. Ultrafine particle emissions, released during thermal treatment of CNFs, were primarily responsible. In contrast, transient increases in respirable particle mass concentration, with a maximum of 1.1 mg m(-3), were due to CNF release through uncontrolled transfer and bagging. Of the applied metrics, our findings suggest that particle mass was probably the most useful and practical metric for monitoring CNF emissions in this facility. Through chemical means, CNFs may be selectively distinguished from other workplace contaminants (Birch et al., in preparation), and for direct-reading monitoring applications, the photometer was found to provide a reasonable estimate of respirable CNF mass concentration. Particle size distribution measurements were conducted with an electrical low-pressure impactor and a fast particle size spectrometer. Results suggest that the dominant CNF mode by particle number lies between 200 and 250 nm for both aerodynamic and mobility equivalent diameters. Significant emissions of CO were also evident in this facility. Exposure control

  7. Atmospheric impact of the 1783-1784 Laki Eruption: Part II Climatic effect of sulphate aerosol

    NASA Astrophysics Data System (ADS)

    Highwood, E. J.; Stevenson, D. S.

    2003-03-01

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

  8. 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.

  9. Aerosol Direct Radiative Forcing in the Southern Appalachian Mountains: Initial Results from the Appalachian Atmospheric Interdisciplinary Research (AppalAIR) Facility

    NASA Astrophysics Data System (ADS)

    Taubman, B.; Sherman, J.; Sheridan, P. J.; Perry, L. B.; Neufeld, H.; Emanuel, R. E.; Tashakkori, R.; Bowman, D.; Long, C.

    2009-12-01

    AppalAIR (Appalachian Atmospheric Interdisciplinary Research, http://appalair.appstate.edu/) is a new interdisciplinary, atmospheric research facility located on the campus of Appalachian State University (1076 m; 36.2° N, 81.7° W) in the southern Appalachian Mountains. The facility was designed to investigate air pollution formation and transport, the relationships among biogenic and anthropogenic inputs to a changing climate, and the effects of these factors on regional ecosystems. AppalAIR is a collaborating member of the NOAA Earth System Research Laboratory Global Monitoring Division (NOAA/ESRL GMD) Collaborative Global Aerosol Network (http://www.esrl.noaa.gov/gmd/aero/net/app/index.html). Measurements are made from a 34 m tower and include aerosol light scattering (3-λ nephelometer) and absorption (3-λ PSAP, 7-λ aethalometer, 6-λ UV aethalometer), particle number concentration (CPC), and aerosol chemistry, size, and morphology using SPME/GC-MS and SEM analyses on 24 h filter samples. Initial results indicate alternating periods of small, highly absorptive (ssa < 0.90) fractal agglomerates and large, highly scattering (ssa > 0.95) spherical particles that are strongly dependent upon the highly variably meteorological patterns that have occurred over the summertime (JJA) in the southeastern U.S. By quantifying the aerosol direct radiative forcing during discrete meteorological patterns as defined by statistical cluster analysis as well as from specific aerosol chemical sources, we are able to extrapolate the results beyond the immediate region.

  10. Case studies on aerosol feedback effects in online coupled chemistry-meteorology models during the 2010 Russian fire event

    NASA Astrophysics Data System (ADS)

    Forkel, Renate; Brunner, Dominik; Balzarini, Alessandra; Baró, Rocio; Hirtl, Marcus; Jiménez-Guerrero, Pedro; Jorba, Oriol; Perez, Juan L.; Pirovano, Guido; San Jose, Roberto; Schröder, Wolfram; Werhahn, Johannes; Wolke, Ralf; Žabkar, Rahela

    2015-04-01

    Aerosol particles are known to have an impact on weather and climate directly via radiation and via their impact on cloud formation and subsequent modified optical properties of clouds. Integrated or "online" coupled regional meteorology-chemistry models like WRF-Chem, COSMO-ART, COSMO-Muscat, EnviroHIRLAM, NMMB/BSC-CTM, RAMS/ICLAMS or WRF-CMAQ are able to account for this impact of aerosol on simulated meteorological variables. However, besides of the meteorological situation simulated effects may also depend on model configuration. In order to analyse these effects and to compare their representation in different models currently used in Europe, multi model simulations were performed for two episodes with high aerosol loads as a coordinated exercise of the COST Action ES1004 (EuMetChem). Here we analyze the first of these two case studies, the severe Russian forest fires in summer 2010. Emission data, boundary conditions, simulation strategy and data output format were harmonized as much as possible to maximize the comparability of the results from the different models. The high aerosol emissions during the summer 2010 Russian wildfire episode led to pronounced feedback effects. For example, the direct aerosol effect lowered the summer mean solar radiation by 20 W m-3 and seasonal mean temperature by 0.25 degrees. This might be considered as a lower limit as it must be taken into account that aerosol concentrations were generally underestimated by the WRF-Chem simulations by up to 50%. The high aerosol concentrations emitted from the wildfires over Russia were found to decrease the small amount of precipitation over Russia during this episode by another 10% to 30% when aerosol cloud interactions were taken into account. The focus of the discussion will be on case study results from WRF-Chem and a comparison with results from COSMO-ART, COSMO-Muscat, and NMMB/BSC-CTM.

  11. Global Impacts of Gas-Phase Chemistry-Aerosol Interactions on Direct Radiative Forcing by Anthropogenic Aerosols and Ozone

    NASA Technical Reports Server (NTRS)

    Liao, Hong; Seinfeld, John H.

    2005-01-01

    We present here a first global modeling study on the influence of gas-phase chemistry/aerosol interactions on estimates of anthropogenic forcing by tropospheric O3 and aerosols. Concentrations of gas-phase species and sulfate, nitrate, ammonium, black carbon, primary organic carbon, secondary organic carbon, sea salt, and mineral dust aerosols in the preindustrial, present-day, and year 2100 (IPCC SRES A2) atmospheres are simulated online in the Goddard Institute for Space Studies general circulation model II' (GISS GCM II'). With fully coupled chemistry and aerosols, the preindustrial, presentday, and year 2100 global burdens of tropospheric ozone are predicted to be 190, 319, and 519 Tg, respectively. The burdens of sulfate, nitrate, black carbon, and organic carbon are predicted respectively to be 0.32. 0.18, 0.01, 0.33 Tg in preindustrial time, 1.40, 0.48, 0.23, 1.60 Tg in presentday, and 1.37, 1.97, 0.54, 3.31 Tg in year 2100. Anthropogenic O3 is predicted to have a globally and annually averaged present-day forcing of +0.22 W m(sup -2) and year 2100 forcing of +0.57 W m(sup -2) at the top of the atmosphere (TOA). Net anthropogenic TOA forcing by internally mixed sulfate, nitrate, organic carbon, and black carbon aerosols is estimated to be virtually zero in the present-day and +0.34 W m(sup -2) in year 2100, whereas it is predicted to be -0.39 W m(sup -2) in present-day and -0.61 W m(sup -2) in year 2100 if the aerosols are externally mixed. Heterogeneous reactions are shown to be important in affecting anthropogenic forcing. When reactions of N2O5, NO3, NO2, and HO2 on aerosols are accounted for, TOA anthropogenic O3 forcing is less by 20-45% in present-day and by 20-32% in year 2100 at mid to high latitudes in the Northern Hemisphere, as compared with values predicted in the absence of heterogeneous gas aerosol reactions. Mineral dust uptake of HNO3 and O3 is shown to have practically no influence on anthropogenic O3 forcing. Heterogeneous reactions of N2Os

  12. Investigation on seasonal variations of aerosol properties and its influence on radiative effect over an urban location in central India

    NASA Astrophysics Data System (ADS)

    Jose, Subin; Gharai, Biswadip; Niranjan, K.; Rao, P. V. N.

    2016-05-01

    Aerosol plays an important role in modulating solar radiation, which are of great concern in perspective of regional climate change. The study analysed the physical and optical properties of aerosols over an urban area and estimated radiative effect using three years in-situ data from sunphotometer, aethalometer and nephelometer as input to radiative transfer model. Aerosols properties indicate the dominance of fine mode aerosols over the study area. However presence of coarse mode aerosols is also found during pre-monsoon [March-April-May]. Daily mean aerosol optical depth showed a minimum during winter [Dec-Jan-Feb] (0.45-0.52) and a maximum during pre-monsoon (0.6-0.7), while single scattering albedo (ω) attains its maximum (0.78 ± 0.05) in winter and minimum (0.67 ± 0.06) during pre-monsoon and asymmetry factor varied in the range between 0.48 ± 0.02 to 0.53 ± 0.04. Episodic events of dust storm and biomass burning are identified by analyzing intrinsic aerosol optical properties like scattering Ångström exponent (SAE) and absorption Ångström exponent (AAE) during the study periods and it has been observed that during dust storm events ω is lower (˜0.77) than that of during biomass burning (˜0.81). The aerosol direct radiative effect at top of the atmosphere during winter is -11.72 ± 3.5 Wm-2, while during pre-monsoon; it is -5.5 ± 2.5 Wm-2, which can be due to observed lower values of ω during pre-monsoon. A large positive enhancement of atmospheric effect of ˜50.53 Wm-2 is observed during pre-monsoon compared to winter. Due to high aerosol loading in pre-monsoon, a twofold negative surface forcing is also observed in comparison to winter.

  13. Use of ARM Mobile Facility (AMF) Data to Study Aerosol Indirect Effects in China

    SciTech Connect

    Li, Zhanqing

    2012-12-19

    General goals: 1) Facilitating the deployment of the ARM Mobile Facility (AMF) and Ancillary Facility (AAF) in China in 2008, 2) Processing, retrieving, improving and analyzing observation data from ground-based, air-borne and space-borne instruments; 3) Conducting a series of studies to gain insights into the direct and indirect effects of these aerosols on radiation, clouds, and precipitation using both

  14. 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.

  15. In situ observations of aerosol and chlorine monoxide after the 1991 eruption of Mount Pinatubo - Effect of reactions on sulfate aerosol

    NASA Technical Reports Server (NTRS)

    Wilson, J. C.; Jonsson, H. H.; Brock, C. A.; Toohey, D. W.; Avallone, L. M.; Baumgardner, D.; Dye, J. E.; Poole, L. R.; Woods, D. C.; Decoursey, R. J.

    1993-01-01

    Highly resolved aerosol size distributions measured from high-altitude aircraft can be used to describe the effect of the 1991 eruption of Mount Pinatubo on the stratospheric aerosol. In some air masses, aerosol mass mixing ratios increased by factors exceeding 100 and aerosol surface area concentrations increased by factors of 30 or more. Increases in aerosol surface area concentration were accompanied by increases in chlorine monoxide at mid-latitudes when confounding factors were controlled. This observation supports the assertion that reactions occurring on the aerosol can increase the fraction of stratospheric chlorine that occurs in ozone-destroying forms.

  16. CALIPSO Observations of Aerosol Properties Near Clouds

    NASA Technical Reports Server (NTRS)

    Marshak, Alexander; Varnai, Tamas; Yang, Weidong

    2010-01-01

    Clouds are surrounded by a transition zone of rapidly changing aerosol properties. Characterizing this zone is important for better understanding aerosol-cloud interactions and aerosol radiative effects as well as for improving satellite measurements of aerosol properties. We present a statistical analysis of a global dataset of CALIPSO (Cloud-Aerosol Lidar and infrared Pathfinder Satellite Observation) Lidar observations over oceans. The results show that the transition zone extends as far as 15 km away from clouds and it is ubiquitous over all oceans. The use of only high confidence level cloud-aerosol discrimination (CAD) data confirms the findings. However, the results underline the need for caution to avoid biases in studies of satellite aerosol products, aerosol-cloud interactions, and aerosol direct radiative effects.

  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.

  18. Effect of tropospheric aerosols upon atmospheric infrared cooling rates

    NASA Technical Reports Server (NTRS)

    Harshvardhan, MR.; Cess, R. D.

    1978-01-01

    The effect of tropospheric aerosols on atmospheric infrared cooling rates is investigated by the use of recent models of infrared gaseous absorption. A radiative model of the atmosphere that incorporates dust as an absorber and scatterer of infrared radiation is constructed by employing the exponential kernel approximation to the radiative transfer equation. Scattering effects are represented in terms of a single scattering albedo and an asymmetry factor. The model is applied to estimate the effect of an aerosol layer made of spherical quartz particles on the infrared cooling rate. Calculations performed for a reference wavelength of 0.55 microns show an increased greenhouse effect, where the net upward flux at the surface is reduced by 10% owing to the strongly enhanced downward emission. There is a substantial increase in the cooling rate near the surface, but the mean cooling rate throughout the lower troposphere was only 10%.

  19. Effects of Ocean Ecosystem on Marine Aerosol-Cloud Interaction

    DOE PAGES

    Meskhidze, Nicholas; Nenes, Athanasios

    2010-01-01

    Using smore » atellite data for the surface ocean, aerosol optical depth (AOD), and cloud microphysical parameters, we show that statistically significant positive correlations exist between ocean ecosystem productivity, the abundance of submicron aerosols, and cloud microphysical properties over different parts of the remote oceans. The correlation coefficient for remotely sensed surface chlorophyll a concentration ([Chl- a ]) and liquid cloud effective radii over productive areas of the oceans varies between − 0.2 and − 0.6 . Special attention is given to identifying (and addressing) problems from correlation analysis used in the previous studies that can lead to erroneous conclusions. A new approach (using the difference between retrieved AOD and predicted sea salt aerosol optical depth, AOD diff ) is developed to explore causal links between ocean physical and biological systems and the abundance of cloud condensation nuclei (CCN) in the remote marine atmosphere. We have found that over multiple time periods, 550 nm AOD diff (sensitive to accumulation mode aerosol, which is the prime contributor to CCN) correlates well with [Chl- a ] over the productive waters of the Southern Ocean. Since [Chl- a ] can be used as a proxy of ocean biological productivity, our analysis demonstrates the role of ocean ecology in contributing CCN, thus shaping the microphysical properties of low-level marine clouds.« less

  20. Effects of mineral dust on the semivolatile inorganic aerosol components in a polluted Megacity

    NASA Astrophysics Data System (ADS)

    Karydis, V. A.; Tsimpidi, A. P.; Fountoukis, C.; Nenes, A.; Zavala, M.; Lei, W.; Molina, L. T.; Pandis, S. N.

    2009-04-01

    Aerosols play a significant role in the atmosphere having adverse impacts on human health and directly affecting air quality, visibility and climate change. One of the most challenging tasks for models is the prediction of the partitioning of the semivolatile inorganic aerosol components (ammonia, nitric acid, hydrochloric acid, etc) between the gas and particulate phases. Moreover, the effects of mineral aerosols in the atmosphere remain largely uncertain. As a result, most current models have serious difficulties in reproducing the observed particulate nitrate and chloride concentrations. The improved aerosol thermodynamic model ISORROPIA II (Fountoukis and Nenes, 2007) simulating explicitly the chemistry of Ca, Mg, and K salts has been linked to the regional chemical transport model PMCAMx (Gaydos et al., 2007). PMCAMx also includes the CMU inorganic aerosol growth module (Gaydos et al., 2003; Koo et al., 2003a) and the VSRM aqueous-phase chemistry module (Fahey and Pandis, 2001). The hybrid approach (Koo et al., 2003b) for modeling aerosol dynamics is applied in order to accurately simulate the inorganic components in the coarse mode. This approach assumes that the smallest particles are in equilibrium, while the condensation/evaporation equation is solved for the larger ones. PMCAMx is applied to the Mexico City Metropolitan Area (MCMA). The emission inventory has been improved and now includes more accurate dust and NaCl emissions. The April 2003 (MCMA Campaign) and the March 2006 (MILAGRO campaign) datasets are used to evaluate the inorganic aerosol module of PMCAMx in order to test our understanding of inorganic aerosol. The results from the new modeling framework are also compared with the results from the previous version of PMCAMx in order to investigate the influence of each of the added features to the formation of the semivolatile inorganic components. References Fountoukis, C. and Nenes, A., (2007). ISORROPIA II: a computationally efficient

  1. The Effect of Recent Aerosol Trends on Solar Radiation in the Central and Southeastern United States: Implications for Regional Hydrology.

    NASA Astrophysics Data System (ADS)

    Cusworth, D.; Mickley, L. J.; Leibensperger, E. M.; Iacono, M. J.

    2015-12-01

    Observations show large increases in summertime (JJA) surface solar radiation (SWdn) over the central and southeastern United States during the last 20 years, as much as a +40 Wm-2 at midday. At the same time, in response to environmental regulations in the early 1990s, emissions of U.S. aerosol precursors have decreased by as much as 60%. Detecting a possible connection between these two trends has been difficult due to the secondary effects of aerosols on cloud concentration and lifetime, and previous efforts have failed to find a direct link. Here we investigate the clear-sky direct effect of decreasing U.S. aerosols on climate, using a radiative transfer model (RRTMG) driven by 1997-2014 measurements of aerosol optical depth at Surface Radiation Budget Network (SURFRAD) sites in the central and southeastern United States. We impose aerosol asymmetry parameters and single scattering albedos from nearby Aerosol Robotic Network (AERONET) sites. Preliminary results indicate that declining aerosols drive a summer noontime change in clear-sky SWdn of +25 Wm-2 since 1997 at Goodwin Creek, MS, accounting for 56% of the observed increase in SWdn at that site. Similarly, we find that aerosols increase clear-sky SWdn by +6.5 Wm-2 in Bondville, IL, which accounts for 21% of the observed SWdn trend there. These results suggest that the climate in these regions of the U.S. may be sensitive to recent reductions in aerosol concentrations, especially during summer months. We also analyze in situ soil measurements from the Illinois Climate Network from 1990-present, and find that a significant decrease in soil moisture (-0.6 m3 m-3 a-1) accompanies the increase in SWdn, implying a link between aerosol trends and regional hydrology. Aerosol reductions are expected to continue in the United States and may further influence regional climate including hydrological factors. Our work has implications for polluted regions outside the U.S., where future reductions in the aerosol burden

  2. 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.

  3. MODIS Aerosol Optical Depth retrieval over land considering surface BRDF effects

    NASA Astrophysics Data System (ADS)

    Wu, Yerong; de Graaf, Martin; Menenti, Massimo

    2016-04-01

    Aerosols in the atmosphere play an important role in the climate system and human health. Retrieval from satellite data, Aerosol Optical Depth (AOD), one of most important indices of aerosol optical properties, has been extensively investigated. Benefiting from the high resolution at spatial and temporal and the maturity of the aerosol retrieval algorithm, MOderate Resolution Imaging Spectroradiometer (MODIS) Dark Target AOD product has been extensively applied in other scientific research such as climate change and air pollution. The latest product - MODIS Collection 6 Dark Target AOD (C6_DT) has been released. However, the accuracy of C6_DT AOD (global mean ±0.03) over land is still too low for the constraint on radiative forcing in the climate system, where the uncertainty should be reduced to ±0.02. The major uncertainty mainly lies on the underestimation/overestimation of the surface contribution to the Top Of Atmosphere (TOA) radiance since a lambertian surface is assumed in the C6_DT land algorithm. In the real world, it requires considering the heterogeneity of the surface reflection in the radiative transfer process. Based on this, we developed a new algorithm to retrieve AOD by considering surface Bidirectional Reflectance Distribution Function (BRDF) effects. The surface BRDF is much more complicated than isotropic reflection, described as 4 elements: directional-directional, directional-hemispherical, hemispherical-directional and hemispherical-hemispherical reflectance, and coupled into radiative transfer equation to generate an accurate top of atmosphere reflectance. The limited MODIS measurements (three channels available) allow us to retrieve only three parameters, which including AOD, the surface directional-directional reflectance and fine aerosol ratio η. The other three elements of the surface reflectance are expected to be constrained by ancillary data and assumptions or "a priori" information since there are more unknowns than MODIS

  4. Spatial distributions and seasonal cycles of aerosol climate effects in India seen in a global climate-aerosol model

    NASA Astrophysics Data System (ADS)

    Henriksson, S. V.; Pietikäinen, J.-P.; Hyvärinen, A.-P.; Räisänen, P.; Kupiainen, K.; Tonttila, J.; Hooda, R.; Lihavainen, H.; O'Donnell, D.; Backman, L.; Klimont, Z.; Laaksonen, A.

    2014-09-01

    Climate-aerosol interactions in India are studied by employing the global climate-aerosol model ECHAM5-HAM and the GAINS inventory for anthropogenic aerosol emissions. Model validation is done for black carbon surface concentrations in Mukteshwar and for features of the monsoon circulation. Seasonal cycles and spatial distributions of radiative forcing and the temperature and rainfall responses are presented for different model setups. While total aerosol radiative forcing is strongest in the summer, anthropogenic forcing is considerably stronger in winter than in summer. Local seasonal temperature anomalies caused by aerosols are mostly negative with some exceptions, e.g., parts of northern India in March-May. Rainfall increases due to the elevated heat pump (EHP) mechanism and decreases due to solar dimming mechanisms (SDMs) and the relative strengths of these effects during different seasons and for different model setups are studied. Aerosol light absorption does increase rainfall in northern India, but effects due to solar dimming and circulation work to cancel the increase. The total aerosol effect on rainfall is negative for northern India in the months of June-August, but during March-May the effect is positive for most model setups. These differences between responses in different seasons might help converge the ongoing debate on the EHPs and SDMs. Due to the complexity of the problem and known or potential sources for error and bias, the results should be interpreted cautiously as they are completely dependent on how realistic the model is. Aerosol-rainfall correlations and anticorrelations are shown not to be a reliable sole argument for deducing causality.

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

    SciTech Connect

    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 transitional 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.

  6. 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; ...

    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

  7. A new chemistry option in WRF/Chem v. 3.4 for the simulation of direct and indirect aerosol effects using VBS: evaluation against IMPACT-EUCAARI data

    NASA Astrophysics Data System (ADS)

    Tuccella, P.; Curci, G.; Grell, G. A.; Visconti, G.; Crumeroylle, S.; Schwarzenboeck, A.; Mensah, A. A.

    2015-02-01

    A parameterization for secondary organic aerosol (SOA) production based on the volatility basis set (VBS) approach has been coupled with microphysics and radiative scheme in WRF/Chem model. The new chemistry option called "RACM/MADE/VBS" was evaluated on a cloud resolving scale against ground-based and aircraft measurements collected during the IMPACT-EUCAARI campaign, and complemented with satellite data from MODIS. The day-to-day variability and the diurnal cycle of ozone (O3) and nitrogen oxides (NOx) at the surface is captured by the model. Surface aerosol mass of sulphate (SO4), nitrate (NO3), ammonium (NH4), and organic matter (OM) is simulated with a correlation larger than 0.55. WRF/Chem captures the vertical profile of the aerosol mass in both the planetary boundary layer (PBL) and free troposphere (FT) as a function of the synoptic condition, but the model does not capture the full range of the measured concentrations. Predicted OM concentration is at the lower end of the observed mass. The bias may be attributable to the missing aqueous chemistry processes of organic compounds, the uncertainties in meteorological fields, the assumption on the deposition velocity of condensable organic vapours, and the uncertainties in the anthropogenic emissions of primary organic carbon. Aerosol particle number concentration (condensation nuclei, CN) is overestimated by a factor 1.4 and 1.7 within PBL and FT, respectively. Model bias is most likely attributable to the uncertainties of primary particle emissions (mostly in the PBL) and to the nucleation rate. The overestimation of simulated cloud condensation nuclei (CCN) is more contained with respect to that of CN. The CCN efficiency, which is a measure of the ability of aerosol particles to nucleate cloud droplets, is underestimated by a factor of 1.5 and 3.8 in the PBL and FT, respectively. The comparison with MODIS data shows that the model overestimates the aerosol optical thickness (AOT). The domain averages (for

  8. Recent Updates on Electronic Cigarette Aerosol and Inhaled Nicotine Effects on Periodontal and Pulmonary Tissues.

    PubMed

    Javed, Fawad; Kellesarian, Sergio V; Sundar, Isaac K; Romanos, Georgios E; Rahman, Irfan

    2017-02-06

    E-cigarette derived inhaled nicotine may contribute to the pathogenesis of periodontal and pulmonary diseases in particular via lung inflammation, injurious and dysregulated repair responses. Nicotine is shown to have anti-proliferative properties and affects fibroblasts in vitro, which may interfere in tissue myofibroblast differentiation in e-cig users. This will affect the ability to heal wounds by decreasing wound contraction. In periodontics, direct exposure to e-vapor has been shown to produce harmful effects in periodontal ligament and gingival fibroblasts in culture. This is due to the generation of reactive oxygen species/aldehydes/carbonyls from e-cig aerosol, leading to protein carbonylation of extracellular matrix and DNA adducts/damage. A limited number of studies regarding the effects of e-cig in oral and lung health are available. However, no reports are available to directly link the deleterious effects on e-cigs, inhaled nicotine, and flavorings aerosol on oral periodontal and pulmonary health in particular to identify the risk of oral diseases by e-cigarettes and nicotine aerosols. This mini-review summarizes the recent perspectives on e-cigarettes including inhaled nicotine effects on several pathophysiological events, such as oxidative stress, DNA damage, innate host response, inflammation, cellular senescence, pro-fibrogenic and dysregulated repair, leading to lung remodeling, oral submucous fibrosis and periodontal diseases. This article is protected by copyright. All rights reserved.

  9. Direct evaluation of aerosol-mass loadings from multispectral extinction data

    NASA Technical Reports Server (NTRS)

    Box, M. A.; Mckellar, B. H. J.

    1978-01-01

    A formula is derived for the evaluation of the total volume of aerosol in a column, and hence for the aerosol columnar mass loading, from multispectral extinction data. This formula is exact in the 'anomalous diffraction' approximation, and reasonably accurate for Mie scattering, over a fairly wide range of refractive indices typical of real aerosols.

  10. Organic aerosols

    SciTech Connect

    Penner, J.E.

    1994-01-01

    Organic aerosols scatter solar radiation. They may also either enhance or decrease concentrations of cloud condensation nuclei. This paper summarizes observed concentrations of aerosols in remote continental and marine locations and provides estimates for the sources of organic aerosol matter. The anthropogenic sources of organic aerosols may be as large as the anthropogenic sources of sulfate aerosols, implying a similar magnitude of direct forcing of climate. The source estimates are highly uncertain and subject to revision in the future. A slow secondary source of organic aerosols of unknown origin may contribute to the observed oceanic concentrations. The role of organic aerosols acting as cloud condensation nuclei (CCN) is described and it is concluded that they may either enhance or decrease the ability of anthropogenic sulfate aerosols to act as CCN.

  11. Observations of the first aerosol indirect effect in shallow cumuli

    SciTech Connect

    Berg, Larry K.; Berkowitz, Carl M.; Barnard, James C.; Senum, Gunar; Springston, Stephen R.

    2011-02-08

    Data from the Cumulus Humilis Aerosol Processing Study (CHAPS) are used to estimate the impact of both aerosol indirect effects and cloud dynamics on the microphysical and optical properties of shallow cumuli observed in the vicinity of Oklahoma City, Oklahoma. Not surprisingly, we find that the amount of light scattered by the clouds is dominated by their liquid water content (LWC), which in turn is driven by cloud dynamics. However, removing the effect of cloud dynamics by examining the scattering normalized by LWC shows a strong sensitivity of scattering to pollutant loading. These results suggest that even moderately sized cities, like Oklahoma City, can have a measureable impact on the optical properties of shallow cumuli.

  12. Multi-Decadal Change of Atmospheric Aerosols and Their Effect on Surface Radiation

    NASA Technical Reports Server (NTRS)

    Chin, Mian; Diehl, Thomas; Tan, Qian; Wild, Martin; Qian, Yun; Yu, Hongbin; Bian, Huisheng; Wang, Weiguo

    2012-01-01

    We present an investigation on multi-decadal changes of atmospheric aerosols and their effects on surface radiation using a global chemistry transport model along with the near-term to long-term data records. We focus on a 28-year time period of satellite era from 1980 to 2007, during which a suite of aerosol data from satellite observations and ground-based remote sensing and in-situ measurements have become available. We analyze the long-term global and regional aerosol optical depth and concentration trends and their relationship to the changes of emissions" and assess the role aerosols play in the multi-decadal change of solar radiation reaching the surface (known as "dimming" or "brightening") at different regions of the world, including the major anthropogenic source regions (North America, Europe, Asia) that have been experiencing considerable changes of emissions, dust and biomass burning regions that have large interannual variabilities, downwind regions that are directly affected by the changes in the source area, and remote regions that are considered to representing "background" conditions.

  13. Observed aerosol-induced radiative effect on plant productivity in the eastern United States

    NASA Astrophysics Data System (ADS)

    Strada, S.; Unger, N.; Yue, X.

    2015-12-01

    We apply satellite observations of aerosol optical depth (AOD) in conjunction with flux tower-derived estimates of gross primary productivity (GPP) to probe the relationship between atmospheric aerosol loading and carbon uptake rate at 10 select sites (4 deciduous broadleaf, 3 cropland, 1 evergreen needle leaf, 1 mixed forest and 1 grassland) on hourly time scales in the growing season in the eastern United States. For deciduous and mixed forests, the aerosol light scattering increases GPP with a maximum effect observed under polluted conditions (AOD >0.6), when diffuse radiation is 40-60%. During midday hours, high AOD conditions (>0.4) enhance plant productivity by ∼13% in deciduous forests. In contrast, we find that high diffuse light fraction does not increase the carbon uptake rate in croplands and grasslands; for these ecosystems, we estimate that high AOD conditions reduce GPP by ∼17% during midday hours. Our findings are consistent with previous studies that have attributed these contrasting response sensitivities to the complex and closed canopy architecture of forests versus crops and grasslands. C4 but not C3 crops may benefit from pollution-induced changes in diffuse and direct light. Further research is needed to investigate the role of local meteorology as a possible confounder in the connection between atmospheric aerosols and plant productivity.

  14. Aerosols optical and physical characteristics and direct radiative forcing during a "Shamal" dust storm, a case study

    NASA Astrophysics Data System (ADS)

    Saeed, T. M.; Al-Dashti, H.; Spyrou, C.

    2013-09-01

    Dust aerosols are analyzed for their optical and physical properties during an episode of dust storm that hit Kuwait on 26 March 2003 when "Iraqi Freedom" military operation was in full swing. The intensity of the dust storm was such that it left a thick suspension of dust throughout the following day, 27 March, resulting in a considerable cooling effect at the surface on both days. Ground-based measurements of aerosol optical thickness reached 3.617 and 4.17 on 26-27 March respectively while Ångstrom coefficient, α870/440, dropped to -0.0234 and -0.0318. Particulate matter concentration of diameter 10 μm or less, PM10, peaked at 4800 μg m-3 during dust storm hours of 26 March. Moderate resolution imaging spectrometer (MODIS) retrieved optical and physical characteristics that exhibited extreme values as well. The synoptic of the dust storm is presented and source regions are identified using total ozone mapping spectrometer (TOMS) aerosol index retrieved images. The vertical profile of the dust layer was simulated using SKIRON atmospheric model. Instantaneous net direct radiative forcing is calculated at top of atmosphere (TOA) and surface level. The thick dust layer of 26 March resulted in cooling the TOA by -60 Wm-2 and surface level by -175 Wm-2 for a surface albedo of 0.35. Slightly higher values were obtained for 27 March due to the increase in aerosol optical thickness. The large reduction in the radiative flux at the surface level had caused a drop in surface temperature by approximately 6 °C below its average value. Radiative heating/cooling rates in the shortwave and longwave bands were also examined. Shortwave heating rate reached a maximum value of 2 °K day-1 between 3 and 5 km, dropped to 1.5 °K day-1 at 6 km and diminished at 8 km. Longwave radiation initially heated the lower atmosphere by a maximum value of 0.2 °K day-1 at surface level, declined sharply at increasing altitude and diminished at 4 km. Above 4 km longwave radiation started to

  15. Tropospheric Aerosols

    NASA Astrophysics Data System (ADS)

    Buseck, P. R.; Schwartz, S. E.

    2003-12-01

    m, PM10=1.1 μg m-3; estimated coefficient of light scattering by particulate matter, σep, at 570 nm=12 Mm-1). (b) High aerosol concentration (PM2.5=43.9 μg m-3; PM10=83.4 μg m-3; estimated σep at 570 nm=245 Mm-1) (reproduced by permission of National Park Service, 2002). Although comprising only a small fraction of the mass of Earth's atmosphere, aerosol particles are highly important constituents of the atmosphere. Special interest has focused on aerosols in the troposphere, the lowest part of the atmosphere, extending from the land or ocean surface typically to ˜8 km at high latitudes, ˜12 km in mid-latitudes, and ˜16 km at low latitudes. That interest arises in large part because of the importance of aerosol particles in geophysical processes, human health impairment through inhalation, environmental effects through deposition, visibility degradation, and influences on atmospheric radiation and climate.Anthropogenic aerosols are thought to exert a substantial influence on Earth's climate, and the need to quantify this influence has sparked much of the current interest in and research on tropospheric aerosols. The principal mechanisms by which aerosols influence the Earth radiation budget are scattering and absorbing solar radiation (the so-called "direct effects") and modifying clouds and precipitation, thereby affecting both radiation and hydrology (the so-called "indirect effects"). Light scattering by aerosols increases the brightness of the planet, producing a cooling influence. Light-absorbing aerosols such as black carbon exert a warming influence. Aerosols increase the reflectivity of clouds, another cooling influence. These radiative influences are quantified as forcings, where a forcing is a perturbation to the energy balance of the atmosphere-Earth system, expressed in units of watts per square meter, W m-2. A warming influence is denoted a positive forcing, and a cooling influence, negative. The radiative direct and indirect forcings by

  16. Dependence of the spectral diffuse-direct irradiance ratio on aerosol spectral distribution and single scattering albedo

    NASA Astrophysics Data System (ADS)

    Kaskaoutis, D. G.; Kambezidis, H. D.; Dumka, U. C.; Psiloglou, B. E.

    2016-09-01

    This study investigates the modification of the clear-sky spectral diffuse-direct irradiance ratio (DDR) as a function of solar zenith angle (SZA), spectral aerosol optical depth (AOD) and single scattering albedo (SSA). The solar spectrum under various atmospheric conditions is derived with Simple Model of the Atmospheric Radiative Transfer of Sunshine (SMARTS) radiative transfer code, using the urban and continental aerosol models as inputs. The spectral DDR can be simulated with great accuracy by an exponentially decreasing curve, while the aerosol optical properties strongly affect the scattering processes in the atmosphere, thus modifying the DDR especially in the ultraviolet (UV) spectrum. Furthermore, the correlation between spectral DDR and spectral AOD can be represented precisely by an exponential function and can give valuable information about the dominance of specific aerosol types. The influence of aerosols on spectral DDR increases with increasing SZA, while the simulations using the urban aerosol model as input in SMARTS are closer to the measurements taken in the Athens urban environment. The SMARTS simulations are interrelated with spectral measurements and can be used for indirect estimations of SSA. Overall, the current work provides some theoretical approximations and functions that help in understanding the dependence of DDR on astronomical and atmospheric parameters.

  17. Simultaneous Retrieval of Aerosol and Surface Optical Properties from Combined Airborne- and Ground-Based Direct and Diffuse Radiometric Measurements

    NASA Technical Reports Server (NTRS)

    Gatebe, C. K.; Dubovik, O.; King, M. D.; Sinyuk, A.

    2010-01-01

    This paper presents a new method for simultaneously retrieving aerosol and surface reflectance properties from combined airborne and ground-based direct and diffuse radiometric measurements. The method is based on the standard Aerosol Robotic Network (AERONET) method for retrieving aerosol size distribution, complex index of refraction, and single scattering albedo, but modified to retrieve aerosol properties in two layers, below and above the aircraft, and parameters on surface optical properties from combined datasets (Cloud Absorption Radiometer (CAR) and AERONET data). A key advantage of this method is the inversion of all available spectral and angular data at the same time, while accounting for the influence of noise in the inversion procedure using statistical optimization. The wide spectral (0.34-2.30 m) and angular range (180 ) of the CAR instrument, combined with observations from an AERONET sunphotometer, provide sufficient measurement constraints for characterizing aerosol and surface properties with minimal assumptions. The robustness of the method was tested on observations made during four different field campaigns: (a) the Southern African Regional Science Initiative 2000 over Mongu, Zambia, (b) the Intercontinental Transport Experiment-Phase B over Mexico City, Mexico (c) Cloud and Land Surface Interaction Campaign over the Atmospheric Radiation Measurement (ARM) Central Facility, Oklahoma, USA, and (d) the Arctic Research of the Composition of the Troposphere from Aircraft and Satellites (ARCTAS) over Elson Lagoon in Barrow, Alaska, USA. The four areas are dominated by different surface characteristics and aerosol types, and therefore provide good test cases for the new inversion method.

  18. War Induced Aerosol Optical, Microphysical and Radiative Effects

    NASA Astrophysics Data System (ADS)

    Munshi, Pavel; Tiwari, Shubhansh

    2017-01-01

    The effect of war on air pollution and climate is assessed in this communication. War today in respect of civil wars and armed conflict in the Middle East area is taken into consideration. Impacts of war are not only in loss of human life and property, but also in the environment. It is well known that war effects air pollution and in the long run contribute to anthropogenic climate change, but general studies on this subject are few because of the difficulties of observations involved. In the current scenario of the ongoing conflict in the Middle East regions, deductions in parameters of atmosphere are discussed. Aerosol Optical Depth, Aerosol loads, Black Carbon, Ozone,Dust, regional haze and many more are analyzed using various satellite data. Multi-model analysis is also studied to verify the analysis. Type segregation of aerosols, in-depth constraints to atmospheric chemistry, biological effects and particularly atmospheric physics in terms of radiative forcing, etc. are discussed. Undergraduate in Earth Sciences.

  19. Delineating the effect of El-Nino Southern Oscillations using oxygen and sulfur isotope anomalies of sulfate aerosols

    NASA Astrophysics Data System (ADS)

    Shaheen, R.; Abaunza Quintero, M. M.; Jackson, T.; McCabe, J.; Savarino, J. P.; Thiemens, M. H.

    2013-12-01

    Sulfate aerosols, unlike greenhouse gases, contribute to global cooling by acting as cloud condensation nuclei in the troposphere and by directly reflecting solar radiation in the stratosphere. To understand the long-term effect of natural and anthropogenic sulfate aerosol on the climate cycle, it is critical to obtain a clear picture of the factors controlling the transport and transformation of sulfate aerosols. We have employed both oxygen triple isotopes and sulfur quadruple isotopes on sulfates from Antarctic ice samples to define the oxidation history, long range transport dynamics, and sources of sulfate aerosols over time. The measurements are used to deconvolve the impact of natural and anthropogenic aerosols on the stratospheric sulfate aerosol composition. Sulfate aerosols were extracted from a snow pit at the South Pole (1979-2002) with a high resolution temporal (6 month) record of the winter and summer seasons covering two largest volcanic events, Pinatubo and El-chichon and three largest ENSO events of the century. All three oxygen and four sulfur isotopes were measured on the extracted sulfate (Shaheen et al., 2013). The high temperature pyrolysis (1000oC) of silver sulfate yielded O2 and SO2. The oxygen triple isotopic composition of the O2 gas was used to determine the oxidation history of sulfate aerosol and SO2 gas obtained during this reaction was utilized to measure sulfur quadruple isotopes following appropriate reaction chemistry (Farquhar et al., 2001). The data revealed that oxygen isotope anomalies in Antarctic aerosols (Δ17O = 0.8-3.7‰) from 1990 to 2001 are strongly linked to the variation in ozone levels in the upper stratosphere/lower stratosphere. The variations in ozone levels are reflective of the intensity of the ENSO events and changes in relative humidity in the atmosphere during this time period. Sulfate concentrations and sulfur quadruple isotopic composition and associated anomalies were used to elucidate the sources of

  20. Correlation between model-calculated anthropogenic aerosols and satellite-derived cloud optical depths: Indication of indirect effect?

    NASA Astrophysics Data System (ADS)

    Chameides, W. L.; Luo, C.; Saylor, R.; Streets, D.; Huang, Y.; Bergin, M.; Giorgi, F.

    2002-05-01

    is a mechanistic coupling between anthropogenic aerosol concentrations and cloud optical properties; one such mechanism is the so-called first and second indirect effect by which aerosols enhance the optical depths and albedos of clouds by increasing the number of droplets within clouds and suppressing precipitation from clouds, respectively. The regressions further suggest that the cloud optical depths increase on average by 0.16 for each 1 mg m-2 increase in the column-integrated anthropogenic aerosol burden. Simple box-model calculations suggest that this is equivalent to a cooling over the model domain from anthropogenic aerosols via the indirect effect that is a factor of about 1.5 times that from the direct effect. Accounting for a possible underestimate in model-simulated aerosol concentrations over the model domain of as much as a factor of 0.6 would lower the estimated cooling from the indirect effect to about 1 times that from the direct effect. In contrast to the results using ISSCP-derived cloud optical depths, the correlation between the model-calculated anthropogenic aerosols and average cloud amount over the model domain was relatively weak and inconsistent. This result arose perhaps because of a cancelling of the competing influences on cloud lifetime and frequency by the second indirect effect and the so-called semi direct effect (i.e., the suppression of clouds by absorbing aerosols).

  1. Aerosol Radiative Effects on Deep Convective Clouds and Associated Radiative Forcing

    NASA Technical Reports Server (NTRS)

    Fan, J.; Zhang, R.; Tao, W.-K.; Mohr, I.

    2007-01-01

    The aerosol radiative effects (ARE) on the deep convective clouds are investigated by using a spectral-bin cloud-resolving model (CRM) coupled with a radiation scheme and an explicit land surface model. The sensitivity of cloud properties and the associated radiative forcing to aerosol single-scattering albedo (SSA) are examined. The ARE on cloud properties is pronounced for mid-visible SSA of 0.85. Relative to the case excluding the ARE, cloud fraction and optical depth decrease by about 18% and 20%, respectively. Cloud droplet and ice particle number concentrations, liquid water path (LWP), ice water path (IWP), and droplet size decrease significantly when the ARE is introduced. The ARE causes a surface cooling of about 0.35 K and significantly high heating rates in the lower troposphere (about 0.6K/day higher at 2 km), both of which lead to a more stable atmosphere and hence weaker convection. The weaker convection and the more desiccation of cloud layers explain the less cloudiness, lower cloud optical depth, LWP and IWP, smaller droplet size, and less precipitation. The daytime-mean direct forcing induced by black carbon is about 2.2 W/sq m at the top of atmosphere (TOA) and -17.4 W/sq m at the surface for SSA of 0.85. The semi-direct forcing is positive, about 10 and 11.2 W/sq m at the TOA and surface, respectively. Both the TOA and surface total radiative forcing values are strongly negative for the deep convective clouds, attributed mostly to aerosol indirect forcing. Aerosol direct and semi-direct effects are very sensitive to SSA. Because the positive semi-direct forcing compensates the negative direct forcing at the surface, the surface temperature and heat fluxes decrease less significantly with the increase of aerosol absorption (decreasing SSA). The cloud fraction, optical depth, convective strength, and precipitation decrease with the increase of absorption, resulting from a more stable and dryer atmosphere due to enhanced surface cooling and

  2. Aerosol properties derived from airborne sky radiance and direct beam measurements in recent NASA and DoE field campaigns

    NASA Astrophysics Data System (ADS)

    Redemann, J.; Flynn, C. J.; Shinozuka, Y.; Russell, P. B.; Kacenelenbogen, M. S.; Segal-Rosenhaimer, M.; Livingston, J. M.; Schmid, B.; Dunagan, S. E.; Johnson, R. R.; LeBlanc, S. E.; Schmidt, S.; Pilewskie, P.; Song, S.

    2014-12-01

    The AERONET (AErosol RObotic NETwork) ground-based suite of sunphotometers provides measurements of spectral aerosol optical depth (AOD), precipitable water and spectral sky radiance, which can be inverted to retrieve aerosol microphysical properties that are critical to assessments of aerosol-climate interactions. Because of data quality criteria and sampling constraints, there are significant limitations to the temporal and spatial coverage of AERONET data and their representativeness for global aerosol conditions. The 4STAR (Spectrometer for Sky-Scanning, Sun-Tracking Atmospheric Research) instrument, jointly developed by NASA Ames and PNNL with NASA Goddard collaboration, combines airborne sun tracking and AERONET-like sky scanning with spectroscopic detection. Being an airborne instrument, 4STAR has the potential to fill gaps in the AERONET data set. The 4STAR instrument operated successfully in the SEAC4RS [Studies of Emissions and Atmospheric Composition, Clouds and Climate Coupling by Regional Surveys] experiment in Aug./Sep. 2013 aboard the NASA DC-8 and in the DoE [Department of Energy]-sponsored TCAP [Two Column Aerosol Project, July 2012 & Feb. 2013] experiment aboard the DoE G-1 aircraft. 4STAR provided direct beam measurements of hyperspectral AOD, columnar trace gas retrievals (H2O, O3, NO2), and the first ever airborne hyperspectral sky radiance scans, which can be inverted to yield the same products as AERONET ground-based observations. In this presentation, we provide an overview of the new 4STAR capabilities, with an emphasis on 26 high-quality sky radiance measurements carried out by 4STAR in SEAC4RS. We compare collocated 4STAR and AERONET sky radiances, as well as their retrievals of aerosol microphysical properties for a subset of the available case studies. We summarize the particle property and airmass characterization studies made possible by the combined 4STAR direct beam and sky radiance observations.

  3. Aerosol Properties Derived from Airborne Sky Radiance and Direct Beam Measurements in Recent NASA and DoE Field Campaigns

    NASA Technical Reports Server (NTRS)

    Redemann, J.; Flynn, C. J.; Shinozuka, Y.; Russell, P. B.; Kacenelenbogen, M.; Segal-Rosenheimer, M.; Livingston, J. M.; Schmid, B.; Dunagan, S. E.; Johnson, R. R.; LeBlanc, S.; Schmidt, S.; Pilewskie, P.; Song, S.

    2014-01-01

    The AERONET (AErosol RObotic NETwork) ground-based suite of sunphotometers provides measurements of spectral aerosol optical depth (AOD), precipitable water and spectral sky radiance, which can be inverted to retrieve aerosol microphysical properties that are critical to assessments of aerosol-climate interactions. Because of data quality criteria and sampling constraints, there are significant limitations to the temporal and spatial coverage of AERONET data and their representativeness for global aerosol conditions.The 4STAR (Spectrometer for Sky-Scanning, Sun-Tracking Atmospheric Research) instrument, jointly developed by NASA Ames and PNNL (Pacific Northwest National Laboratory) with NASA Goddard collaboration, combines airborne sun tracking and AERONET-like sky scanning with spectroscopic detection. Being an airborne instrument, 4STAR has the potential to fill gaps in the AERONET data set. The 4STAR instrument operated successfully in the SEAC4RS (Studies of Emissions and Atmospheric Composition, Clouds and Climate Coupling by Regional Surveys) experiment in Aug./Sep. 2013 aboard the NASA DC-8 and in the DoE (Department of Energy)-sponsored TCAP (Two Column Aerosol Project, July 2012 & Feb. 2013) experiment aboard the DoE G-1 aircraft. 4STAR provided direct beam measurements of hyperspectral AOD, columnar trace gas retrievals (H2O, O3, NO2), and the first ever airborne hyperspectral sky radiance scans, which can be inverted to yield the same products as AERONET ground-based observations. In this presentation, we provide an overview of the new 4STAR capabilities, with an emphasis on 26 high-quality sky radiance measurements carried out by 4STAR in SEAC4RS. We compare collocated 4STAR and AERONET sky radiances, as well as their retrievals of aerosol microphysical properties for a subset of the available case studies. We summarize the particle property and air-mass characterization studies made possible by the combined 4STAR direct beam and sky radiance

  4. Meteorological and aerosol effects on marine cloud microphysical properties

    NASA Astrophysics Data System (ADS)

    Sanchez, K. J.; Russell, L. M.; Modini, R. L.; Frossard, A. A.; Ahlm, L.; Corrigan, C. E.; Roberts, G. C.; Hawkins, L. N.; Schroder, J. C.; Bertram, A. K.; Zhao, R.; Lee, A. K. Y.; Lin, J. J.; Nenes, A.; Wang, Z.; Wonaschütz, A.; Sorooshian, A.; Noone, K. J.; Jonsson, H.; Toom, D.; Macdonald, A. M.; Leaitch, W. R.; Seinfeld, J. H.

    2016-04-01

    Meteorology and microphysics affect cloud formation, cloud droplet distributions, and shortwave reflectance. The Eastern Pacific Emitted Aerosol Cloud Experiment and the Stratocumulus Observations of Los-Angeles Emissions Derived Aerosol-Droplets studies provided measurements in six case studies of cloud thermodynamic properties, initial particle number distribution and composition, and cloud drop distribution. In this study, we use simulations from a chemical and microphysical aerosol-cloud parcel (ACP) model with explicit kinetic drop activation to reproduce observed cloud droplet distributions of the case studies. Four cases had subadiabatic lapse rates, resulting in fewer activated droplets, lower liquid water content, and higher cloud base height than an adiabatic lapse rate. A weighted ensemble of simulations that reflect measured variation in updraft velocity and cloud base height was used to reproduce observed droplet distributions. Simulations show that organic hygroscopicity in internally mixed cases causes small effects on cloud reflectivity (CR) (<0.01), except for cargo ship and smoke plumes, which increased CR by 0.02 and 0.07, respectively, owing to their high organic mass fraction. Organic hygroscopicity had larger effects on droplet concentrations for cases with higher aerosol concentrations near the critical diameter (namely, polluted cases with a modal peak near 0.1 µm). Differences in simulated droplet spectral widths (k) caused larger differences in CR than organic hygroscopicity in cases with organic mass fractions of 60% or less for the cases shown. Finally, simulations from a numerical parameterization of cloud droplet activation suitable for general circulation models compared well with the ACP model, except under high organic mass fraction.

  5. Observed aerosol effects on marine cloud nucleation and supersaturation

    NASA Astrophysics Data System (ADS)

    Russell, Lynn M.; Sorooshian, Armin; Seinfeld, John H.; Albrecht, Bruce A.; Nenes, Athanasios; Leaitch, W. Richard; Macdonald, Anne Marie; Ahlm, Lars; Chen, Yi-Chun; Coggon, Matthew; Corrigan, Ashley; Craven, Jill S.; Flagan, Richard C.; Frossard, Amanda A.; Hawkins, Lelia N.; Jonsson, Haflidi; Jung, Eunsil; Lin, Jack J.; Metcalf, Andrew R.; Modini, Robin; Mülmenstädt, Johannes; Roberts, Greg C.; Shingler, Taylor; Song, Siwon; Wang, Zhen; Wonaschütz, Anna

    2013-05-01

    Aerosol particles in the marine boundary layer include primary organic and salt particles from sea spray and combustion-derived particles from ships and coastal cities. These particle types serve as nuclei for marine cloud droplet activation, although the particles that activate depend on the particle size and composition as well as the supersaturation that results from cloud updraft velocities. The Eastern Pacific Emitted Aerosol Cloud Experiment (EPEACE) 2011 was a targeted aircraft campaign to assess how different particle types nucleate cloud droplets. As part of E-PEACE 2011, we studied the role of marine particles as cloud droplet nuclei and used emitted particle sources to separate particle-induced feedbacks from dynamical variability. The emitted particle sources included shipboard smoke-generated particles with 0.05-1 μm diameters (which produced tracks measured by satellite and had drop composition characteristic of organic smoke) and combustion particles from container ships with 0.05-0.2 μm diameters (which were measured in a variety of conditions with droplets containing both organic and sulfate components) [1]. Three central aspects of the collaborative E-PEACE results are: (1) the size and chemical composition of the emitted smoke particles compared to ship-track-forming cargo ship emissions as well as background marine particles, with particular attention to the role of organic particles, (2) the characteristics of cloud track formation for smoke and cargo ships, as well as the role of multi-layered low clouds, and (3) the implications of these findings for quantifying aerosol indirect effects. For comparison with the E-PEACE results, the preliminary results of the Stratocumulus Observations of Los-Angeles Emissions Derived Aerosol-Droplets (SOLEDAD) 2012 provided evidence of the cloud-nucleating roles of both marine organic particles and coastal urban pollution, with simultaneous measurements of the effective supersaturations of the clouds in the

  6. Analysis of Measurement Requirements for the Aerosol Indirect Effect: A Synthesis of Observations and Modeling

    NASA Astrophysics Data System (ADS)

    Feingold, G.; Previdi, M.; Veron, D. E.

    2003-12-01

    The aerosol indirect effect has been measured for some time now by satellite remote sensors, and more recently by surface-based remote sensors. The indirect effect is often expressed in terms of a relative change in drop size for a relative change in aerosol optical depth or extinction. Here we present some recent results of surface based remote sensing of the indirect effect and assess whether aerosol optical depth or extinction is a suitable proxy for the aerosol affecting drop formation. To do so, we use multiple realizations of a cloud model to investigate the sensitivity of cloud drop effective radius re to aerosol parameters (size distribution and composition) and dynamical parameters (updraft and liquid water content). A breakdown of the individual aerosol terms contributing to drop size change shows that use of aerosol extinction as a proxy for size distribution and composition tends to underestimate the magnitude of the first indirect effect. The use of the aerosol index alleviates this problem somewhat. We show that re is most sensitive to cloud liquid water, a parameter often ignored in indirect effect analyses. The relative importance of the other parameters varies for different conditions but aerosol concentration Na is consistently important. Updraft plays an increasingly important role under high aerosol loadings. Requirements for measuring the indirect effect over polluted continents are shown to be more stringent than those over cleaner, remote oceans. This may influence interpretation of current satellite and surface remote measurements of the indirect effect.

  7. 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.

  8. Seasonal variations of aerosol optical properties, vertical distribution and associated radiative effects in the Yangtze Delta Region of China

    SciTech Connect

    Liu, Jianjun; Zheng, Youfei; Li, Zhanqing; Flynn, Connor J.; Cribb, Maureen

    2012-02-09

    Four years of columnar aerosol particle optical properties (2006 to 2009) and one year database worth of aerosol particle vertical profile of 527 nm extinction coefficient (June 2008 to May 2009) are analyzed at Taihu in the central Yangtze Delta region in eastern China. Seasonal variations of aerosol optical properties, vertical distribution, and influence on shortwave radiation and heating rates were investigated. Multiyear variations of aerosol optical depths (AOD), Angstrom exponents, single scattering albedo (SSA) and asymmetry factor (ASY) are analyzed, together with the vertical profile of aerosol extinction. AOD is largest in summer and smallest in winter. SSAs exhibit weak seasonal variation with the smallest values occurring during winter and the largest during summer. The vast majority of aerosol particles are below 2 km, and about 62%, 67%, 67% and 83% are confined to below 1 km in spring, summer, autumn and winter, respectively. Five-day back trajectory analyses show that the some aerosols aloft are traced back to northern/northwestern China, as far as Mongolia and Siberia, in spring, autumn and winter. The presence of dust aerosols were identified based on the linear depolarization measurements together with other information (i.e., back trajectory, precipitation, aerosol index). Dust strongly impacts the vertical particle distribution in spring and autumn, with much smaller effects in winter. The annual mean aerosol direct shortwave radiative forcing (efficiency) at the bottom, top and within the atmosphere are -34.8 {+-} 9.1 (-54.4 {+-} 5.3), -8.2 {+-} 4.8 (-13.1 {+-} 1.5) and 26.7 {+-} 9.4 (41.3 {+-} 4.6) W/m{sup 2} (Wm{sup -2} T{sup -1}), respectively. The mean reduction in direct and diffuse radiation reaching surface amount to 109.2 {+-} 49.4 and 66.8 {+-} 33.3 W/m{sup 2}, respectively. Aerosols significantly alter the vertical profile of solar heating, with great implications for atmospheric stability and dynamics within the lower troposphere.

  9. Effect of aging on morphology, hygroscopicity, and optical properties of soot aerosol

    NASA Astrophysics Data System (ADS)

    Khalizov, A. F.; Xue, H.; Pagels, J.; McMurry, P. H.; Zhang, R.

    2009-12-01

    Soot from incomplete combustion represents one of the major forms of particulate matter pollution, profoundly impacting human health, air quality, and climate. The direct and indirect radiative effects of soot aerosol depend on particle composition and morphology, which may vary significantly when aerosol is subjected to atmospheric aging. We will present an overview of a comprehensive set of experimental measurements performed in our laboratory at Texas A&M to study the effect of internal mixing with atmospheric species on morphology, hygroscopicity, and optical properties of combustion soot. In our experiments, size-classified soot aerosol was exposed to 0.1 - 1000 ppb (part per billion) mixing ratios of sulfuric acid and dicarboxylic organic acids and resulting changes particle morphology and mixing state under dry and humid conditions were characterized through mass-mobility measurements by aerosol particle mass analyzer (APM) and tandem differential mobility analyzer (TDMA). Light absorption and scattering cross-sections for well-characterized fresh and coated soot aerosol were derived using a cavity ring-down spectrometer and an integrating nephelometer in order to assess the effect of atmospheric processing on the radiative properties of atmospheric soot. Internally mixed soot shows significant changes in particle morphology, increasing with the mass fraction of the coating material and relative humidity. Restructuring was the strongest for aggregates coated by sulfuric and glutaric acids whereas succinic acid coating did not result in observable morphology change. Sulfuric acid - coated particles experienced large hygroscopic growth at sub-saturated conditions and activated to cloud droplets at atmospherically relevant supersaturations. Furthermore, coating and subsequent hygroscopic growth considerably altered the optical properties of soot aerosol, increasing light scattering and absorption cross-sections. We found that irreversible restructuring of soot

  10. Effect of Aerosol Size and Hygroscopicity on Aerosol Optical Depth in the Southeastern United States

    NASA Astrophysics Data System (ADS)

    Brock, Charles; Wagner, Nick; Gordon, Timothy

    2016-04-01

    Aerosol optical depth (AOD) is affected by the size, optical characteristics, and hygroscopicity of particles, confounding attempts to link remote sensing observations of AOD to measured or modeled aerosol mass concentrations. In situ airborne observations of aerosol optical, chemical, microphysical and hygroscopic properties were made in the southeastern United States in the daytime in summer 2013. We use these observations to constrain a simple model that is used to test the sensitivity of AOD to the various measured parameters. As expected, the AOD was found to be most sensitive to aerosol mass concentration and to aerosol water content, which is controlled by aerosol hygroscopicity and the ambient relative humidity. However, AOD was also fairly sensitive to the mean particle diameter and the width of the size distribution. These parameters are often prescribed in global models that use simplified modal parameterizations to describe the aerosol, suggesting that the values chosen could substantially bias the calculated relationship between aerosol mass and optical extinction, AOD, and radiative forcing.

  11. Effects of chemical aging on global secondary organic aerosol using the volatility basis set approach

    NASA Astrophysics Data System (ADS)

    Jo, D. S.; Park, R. J.; Kim, M. J.; Spracklen, D. V.

    2013-12-01

    A global 3-D chemical transport model (GEOS-Chem) is used with the volatility basis set (VBS) approach to examine the effects of chemical aging on global secondary organic aerosol (SOA) concentrations and budgets. We present full-year simulations and their comparisons with the global aerosol mass spectrometer (AMS) dataset, the Interagency Monitoring of Protected Visual Environments (IMPROVE) dataset from the United States, the European Monitoring and Evaluation Programme (EMEP) dataset from Europe, and water-soluble organic carbon observation data collected over East Asia. Using different chemical aging constants, we find that the model results with 4 × 10-11 cm3 molecule-1 s-1 are in better agreement with all observations relative to the model results with other aging constants, without aging, and with the two-product approach. The model simulations are improved when chemical aging is considered, especially for rural regions. However, the simulations still underestimate observed oxygenated organic aerosol (OOA) in urban areas. Two sensitivity simulations including semi-volatile primary organic aerosol (POA) were conducted. We find that including semi-volatile POA improves the model in terms of the hydrogen-like organic aerosol (HOA) to OOA ratio. However, the total OA concentrations are not improved. The total SOA production is considerably increased by 53%, from 26.0 to 39.9 Tg yr-1, after considering chemical aging, remaining lower than top-down estimates of SOA production. Direct radiative forcing (DRF) increases by -0.07 W m-2 due to the chemical aging of SOA, which is comparable to the mean DRF (-0.13 W m-2) of OA from the AeroCom multi-model study. This result indicates considerable global and, more importantly, regional climate implications. For example, the regional DRF change due to chemical aging of SOA in the eastern US is -0.29 W m-2, which is 4 times greater in magnitude than the global mean value.

  12. Effects of flame made zinc oxide particles in human lung cells - a comparison of aerosol and suspension exposures

    PubMed Central

    2012-01-01

    Background Predominantly, studies of nanoparticle (NPs) toxicology in vitro are based upon the exposure of submerged cell cultures to particle suspensions. Such an approach however, does not reflect particle inhalation. As a more realistic simulation of such a scenario, efforts were made towards direct delivery of aerosols to air-liquid-interface cultivated cell cultures by the use of aerosol exposure systems. This study aims to provide a direct comparison of the effects of zinc oxide (ZnO) NPs when delivered as either an aerosol, or in suspension to a triple cell co-culture model of the epithelial airway barrier. To ensure dose–equivalence, ZnO-deposition was determined in each exposure scenario by atomic absorption spectroscopy. Biological endpoints being investigated after 4 or 24h incubation include cytotoxicity, total reduced glutathione, induction of antioxidative genes such as heme-oxygenase 1 (HO–1) as well as the release of the (pro)-inflammatory cytokine TNFα. Results Off-gases released as by-product of flame ZnO synthesis caused a significant decrease of total reduced GSH and induced further the release of the cytokine TNFα, demonstrating the influence of the gas phase on aerosol toxicology. No direct effects could be attributed to ZnO particles. By performing suspension exposure to avoid the factor “flame-gases”, particle specific effects become apparent. Other parameters such as LDH and HO–1 were not influenced by gaseous compounds: Following aerosol exposure, LDH levels appeared elevated at both timepoints and the HO–1 transcript correlated positively with deposited ZnO-dose. Under submerged conditions, the HO–1 induction scheme deviated for 4 and 24h and increased extracellular LDH was found following 24h exposure. Conclusion In the current study, aerosol and suspension-exposure has been compared by exposing cell cultures to equivalent amounts of ZnO. Both exposure strategies differ fundamentally in their dose–response pattern

  13. Effect of aerosol number concentration on cloud droplet dispersion: An LES study and implications for aerosol indirect forcing

    NASA Astrophysics Data System (ADS)

    Lu, M.; Seinfeld, J. H.

    2005-12-01

    Through three-dimensional LES simulations of marine stratocumulus we explore the factors that control the cloud spectral relative dispersion (ratio of cloud droplet spectral width to the mean radius of the distribution) as a function of aerosol number concentration and the extent to which the relative dispersion either enhances or mitigates the Twomey effect. We find that relative dispersion decreases with increasing aerosol number concentration (for aerosol number concentrations less than about 1000 cm- 3) because smaller droplets resulting from higher aerosol number concentrations inhibit precipitation and lead to: (1) less spectral broadening by suppressed collision and coalescence processes; and (2) more spectral narrowing by droplet condensational growth at higher updraft velocity, because reduced drizzle latent heating at cloud top results in increased boundary layer turbulent kinetic energy production by buoyancy and thereby stronger turbulence. Increased spectral broadening owing to increased cloud-top entrainment mixing, also as a result of increased boundary layer turbulence, is relatively insignificant compared with (1) and (2). The coefficient k, an important parameter that relates cloud droplet effective radius and volume mean radius in large-scale models, is a function of skewness and relative dispersion of the distribution and is negatively correlated with relative dispersion. Increasing k with increasing aerosol number concentration leads to maximum enhancement of the cloud susceptibility (the change of cloud optical depth due to change of cloud droplet number concentration) over that attributable to the Twomey effect alone by about 4.2% and 39% for simulated FIRE and ASTEX cases, respectively.

  14. Aerosol effect on the evolution of the thermodynamic properties of warm convective cloud fields

    PubMed Central

    Dagan, Guy; Koren, Ilan; Altaratz, Orit; Heiblum, Reuven H.

    2016-01-01

    Convective cloud formation and evolution strongly depend on environmental temperature and humidity profiles. The forming clouds change the profiles that created them by redistributing heat and moisture. Here we show that the evolution of the field’s thermodynamic properties depends heavily on the concentration of aerosol, liquid or solid particles suspended in the atmosphere. Under polluted conditions, rain formation is suppressed and the non-precipitating clouds act to warm the lower part of the cloudy layer (where there is net condensation) and cool and moisten the upper part of the cloudy layer (where there is net evaporation), thereby destabilizing the layer. Under clean conditions, precipitation causes net warming of the cloudy layer and net cooling of the sub-cloud layer (driven by rain evaporation), which together act to stabilize the atmosphere with time. Previous studies have examined different aspects of the effects of clouds on their environment. Here, we offer a complete analysis of the cloudy atmosphere, spanning the aerosol effect from instability-consumption to enhancement, below, inside and above warm clouds, showing the temporal evolution of the effects. We propose a direct measure for the magnitude and sign of the aerosol effect on thermodynamic instability. PMID:27929097

  15. Aerosol effect on the evolution of the thermodynamic properties of warm convective cloud fields

    NASA Astrophysics Data System (ADS)

    Dagan, Guy; Koren, Ilan; Altaratz, Orit; Heiblum, Reuven H.

    2016-12-01

    Convective cloud formation and evolution strongly depend on environmental temperature and humidity profiles. The forming clouds change the profiles that created them by redistributing heat and moisture. Here we show that the evolution of the field’s thermodynamic properties depends heavily on the concentration of aerosol, liquid or solid particles suspended in the atmosphere. Under polluted conditions, rain formation is suppressed and the non-precipitating clouds act to warm the lower part of the cloudy layer (where there is net condensation) and cool and moisten the upper part of the cloudy layer (where there is net evaporation), thereby destabilizing the layer. Under clean conditions, precipitation causes net warming of the cloudy layer and net cooling of the sub-cloud layer (driven by rain evaporation), which together act to stabilize the atmosphere with time. Previous studies have examined different aspects of the effects of clouds on their environment. Here, we offer a complete analysis of the cloudy atmosphere, spanning the aerosol effect from instability-consumption to enhancement, below, inside and above warm clouds, showing the temporal evolution of the effects. We propose a direct measure for the magnitude and sign of the aerosol effect on thermodynamic instability.

  16. Aerosol effects on clouds, convection and precipitation in the chemistry-climate model EMAC.

    NASA Astrophysics Data System (ADS)

    Chang, D. Y.; Steil, B.; Tost, H.; Lelieveld, J.

    2014-12-01

    This study addresses aerosol effects on clouds and precipitation using the EMAC atmospheric chemistry general circulation model. Aerosol-cloud interactions are explicitly considered in two prognostic cloud droplet nucleation schemes, i.e., applying an osmotic model and the κ method. The two schemes have rather different effects on cloud properties such as cloud droplet number and size distribution, cloud water content, and cloud optical properties. Much higher cloud droplet number concentrations (CDNC) are simulated with the osmotic model compared to the k method, leading to substantially different cloud radiative effects and consequently convection and precipitation, particularly over the continents. The osmotic model simulation yields an about 6.5 W/m2 stronger cooling effect over land than the κ method, with three times higher CDNC. The convective activity in terms of convective available potential energy (CAPE) is decreased by 20%, which corresponds to a decrease in convective precipitation by 23% in favor of large-scale precipitation. Note that in the current model setup only large-scale clouds are directly affected by interactions with aerosols, while in convection and associated precipitation are affected indirectly.

  17. Aerosol effect on the evolution of the thermodynamic properties of warm convective cloud fields.

    PubMed

    Dagan, Guy; Koren, Ilan; Altaratz, Orit; Heiblum, Reuven H

    2016-12-08

    Convective cloud formation and evolution strongly depend on environmental temperature and humidity profiles. The forming clouds change the profiles that created them by redistributing heat and moisture. Here we show that the evolution of the field's thermodynamic properties depends heavily on the concentration of aerosol, liquid or solid particles suspended in the atmosphere. Under polluted conditions, rain formation is suppressed and the non-precipitating clouds act to warm the lower part of the cloudy layer (where there is net condensation) and cool and moisten the upper part of the cloudy layer (where there is net evaporation), thereby destabilizing the layer. Under clean conditions, precipitation causes net warming of the cloudy layer and net cooling of the sub-cloud layer (driven by rain evaporation), which together act to stabilize the atmosphere with time. Previous studies have examined different aspects of the effects of clouds on their environment. Here, we offer a complete analysis of the cloudy atmosphere, spanning the aerosol effect from instability-consumption to enhancement, below, inside and above warm clouds, showing the temporal evolution of the effects. We propose a direct measure for the magnitude and sign of the aerosol effect on thermodynamic instability.

  18. 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

    2017-02-01

    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

  19. 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

  20. Combined effects of organic aerosol loading and fog processing on organic aerosols oxidation and composition

    NASA Astrophysics Data System (ADS)

    Chakraborty, Abhishek; Tripathi, Sachchida; Gupta, Tarun

    2016-04-01

    Fog is a natural meteorological phenomenon that occurs throughout the world, it contains substantial quantity of liquid water and generally seen as a natural cleansing agent but it also has the potential to form highly oxidized secondary organic aerosols (SOA) via aqueous processing of ambient aerosols. On the other hand higher organic aerosols (OA) loading tend to decrease the overall oxidation level (O/C) of the particle phase organics, due to enhanced partitioning of less oxidized organics from gas to particle phase. However, combined impact of these two parameters; aqueous oxidation and OA loading, on the overall oxidation ratio (O/C) of ambient OA has never been studied. To assess this, real time ambient sampling using HR-ToF-AMS was carried out at Kanpur, India from 15 December 2014 - 10 February 2015. In first 3 weeks of this campaign, very high OA loading is (134 ± 42 μg/m3) observed (termed as high loading or HL period) while loading is substantially reduced from 2nd January, 2016 (56 ± 20 μg/m3, termed as low loading or LL period) . However, both the loading period was affected by several fog episodes (10 in HL and 7 in LL), thus providing the opportunity of studying the combined effects of fog and OA loading on OA oxidation. It is found that O/C ratio is very strongly anti-correlated with OA loading in both the loading period, however, slope of this ant-correlation is much steep during HL period than in LL period. Source apportionment of OA revealed that there is drastic change in the types of OA from HL to LL period, clearly indicating difference in OA composition from HL to LL period. During foggy night continuous oxidation of OA is observed from early evening to early morning with 15-20% enhancement in O/C ratio, while the same is absent during non-foggy period, clearly indicating the efficient fog processing of ambient OA. It is also found that night time fog aqueous oxidation can be as effective as daytime photo chemistry in oxidation of OA. Fog

  1. Atmospheric aerosols: Their Optical Properties and Effects (supplement)

    NASA Technical Reports Server (NTRS)

    1976-01-01

    A digest of technical papers is presented. Topics include aerosol size distribution from spectral attenuation with scattering measurements; comparison of extinction and backscattering coefficients for measured and analytic stratospheric aerosol size distributions; using hybrid methods to solve problems in radiative transfer and in multiple scattering; blue moon phenomena; absorption refractive index of aerosols in the Denver pollution cloud; a two dimensional stratospheric model of the dispersion of aerosols from the Fuego volcanic eruption; the variation of the aerosol volume to light scattering coefficient; spectrophone in situ measurements of the absorption of visible light by aerosols; a reassessment of the Krakatoa volcanic turbidity, and multiple scattering in the sky radiance.

  2. Direct observations of organic aerosols in common wintertime hazes in North China: insights into direct emissions from Chinese residential stoves

    NASA Astrophysics Data System (ADS)

    Chen, Shurui; Xu, Liang; Zhang, Yinxiao; Chen, Bing; Wang, Xinfeng; Zhang, Xiaoye; Zheng, Mei; Chen, Jianmin; Wang, Wenxing; Sun, Yele; Fu, Pingqing; Wang, Zifa; Li, Weijun

    2017-01-01

    Many studies have focused on the physicochemical properties of aerosol particles in unusually severe haze episodes in North China instead of the more frequent and less severe hazes. Consistent with this lack of attention, the morphology and mixing state of organic matter (OM) particles in the frequent light and moderate (L & M) hazes in winter in the North China Plain (NCP) have not been examined, even though OM dominates these fine particles. In the present work, morphology, mixing state, and size of organic aerosols in the L & M hazes were systematically characterized using transmission electron microscopy coupled with energy-dispersive X-ray spectroscopy, atomic force microscopy, and nanoscale secondary ion mass spectrometer, with the comparisons among an urban site (Jinan, S1), a mountain site (Mt. Tai, S2), and a background island site (Changdao, S3) in the same hazes. Based on their morphologies, the OM particles were divided into six different types: spherical (type 1), near-spherical (type 2), irregular (type 3), domelike (type 4), dispersed-OM (type 5), and OM-coating (type 6). In the three sampling sites, types 1-3 of OM particles were most abundant in the L & M hazes and most of them were internally mixed with non-OM particles. The abundant near-spherical OM particles with higher sphericity and lower aspect ratio indicate that these primary OM particles formed in the cooling process after polluted plumes were emitted from coal combustion and biomass burning. Based on the Si-O-C ratio in OM particles, we estimated that 71 % of type 1-3 OM particles were associated with coal combustion. Our result suggests that coal combustion in residential stoves was a widespread source from urban to rural areas in NCP. Average OM thickness which correlates with the age of the air masses in type 6 particles only slightly increased from S1 to S2 to S3, suggesting that the L & M hazes were usually dry (relative humidity < 60 %) with weak photochemistry and

  3. Effects of aerosol from biomass burning on the global radiation budget

    NASA Technical Reports Server (NTRS)

    Penner, Joyce E.; Dickinson, Robert E.; O'Neill, Christine A.

    1992-01-01

    An analysis is made of the likely contribution of smoke particles from biomass burning to the global radiation balance. These particles act to reflect solar radiation directly; they also can act as cloud condensation nuclei, increasing the reflectivity of clouds. Together these effects, although uncertain, may add up globally to a cooling effect as large as 2 watts per square meter, comparable to the estimated contribution to sulfate aerosols. Anthropogenic increases of smoke emission thus may have helped weaken the net greenhouse warming from anthropogenic trace gases.

  4. 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

  5. The effect of organic aerosol material on aerosol reactivity towards ozone

    NASA Astrophysics Data System (ADS)

    Batenburg, Anneke; Gaston, Cassandra; Thornton, Joel; Virtanen, Annele

    2015-04-01

    After aerosol particles are formed or emitted into the atmosphere, heterogeneous reactions with gaseous oxidants cause them to 'age'. Aging can change aerosol properties, such as the hygroscopicity, which is an important parameter in how the particles scatter radiation and form clouds. Conversely, heterogeneous reactions on aerosol particles play a significant role in the cycles of various atmospheric trace gases. Organic compounds, a large part of the total global aerosol matter, can exist in liquid or amorphous (semi)solid physical phases. Different groups have shown that reactions with ozone (O3) can be limited by bulk diffusion in organic aerosol, particularly in viscous, (semi)solid materials, and that organic coatings alter the surface interactions between gas and aerosol particles. We aim to better understand and quantify how the viscosity and phase of organic aerosol matter affect gas-particle interactions. We have chosen the reaction of O3 with particles composed of a potassium iodide (KI) core and a variable organic coating as a model system. The reaction is studied in an aerosol flow reactor that consists of a laminar flow tube and a movable, axial injector for the injection of O3. The aerosol-containing air is inserted at the tube's top. The interaction length (and therefore time), between the particles and the O3 can be varied by moving the injector. Alternatively, the production of aerosol particles can be modulated. The remaining O3 concentration is monitored from the bottom of the tube and particle concentrations are measured simultaneously, which allows us to calculate the reactive uptake coefficient γ. We performed exploratory experiments with internally mixed KI and polyethylene glycol (PEG) particles at the University of Washington (UW) in a setup with a residence time around 50 s. Aerosol particles were generated in an atomizer from solutions with varying concentrations of KI and PEG and inserted into the flow tube after they were diluted and

  6. Biological aerosol effects on clouds and precipitation

    NASA Astrophysics Data System (ADS)

    Hallar, A. Gannet; Huffman, J. Alex; Fridlind, Ann

    2012-12-01

    Bioaerosol Effects on Clouds Workshop;Steamboat Springs, Colorado, 5-6August 2012 Bioaerosols such as bacteria have been proposed as significant contributors to cloud ice nucleation, but too little is known about the properties and impacts of bioaerosol and other ice nuclei to make reliable conclusions about their wide-scale impact on clouds and precipitation. During late summer an international group of 40 participants met at a Steamboat Springs ski resort to share perspectives on bioaerosol sources, activity, and influence on clouds. Participants who were invited collectively spanned a broad range of expertise, including atmospheric chemistry, microbiology, micrometeorology, and cloud physics, as well as a broad range of research approaches, including laboratory measurement, field measurement, and modeling. Tours of Storm Peak Laboratory (http://www.stormpeak.dri.edu) were offered before and after the workshop.

  7. Internally Consistent MODIS Estimate of Aerosol Clear-Sky Radiative Effect Over the Global Oceans

    NASA Technical Reports Server (NTRS)

    Remer, Lorraine A.; Kaufman, Yoram J.

    2004-01-01

    Modern satellite remote sensing, and in particular the MODerate resolution Imaging Spectroradiometer (MODIS), offers a measurement-based pathway to estimate global aerosol radiative effects and aerosol radiative forcing. Over the Oceans, MODIS retrieves the total aerosol optical thickness, but also reports which combination of the 9 different aerosol models was used to obtain the retrieval. Each of the 9 models is characterized by a size distribution and complex refractive index, which through Mie calculations correspond to a unique set of single scattering albedo, assymetry parameter and spectral extinction for each model. The combination of these sets of optical parameters weighted by the optical thickness attributed to each model in the retrieval produces the best fit to the observed radiances at the top of the atmosphere. Thus the MODIS Ocean aerosol retrieval provides us with (1) An observed distribution of global aerosol loading, and (2) An internally-consistent, observed, distribution of aerosol optical models that when used in combination will best represent the radiances at the top of the atmosphere. We use these two observed global distributions to initialize the column climate model by Chou and Suarez to calculate the aerosol radiative effect at top of the atmosphere and the radiative efficiency of the aerosols over the global oceans. We apply the analysis to 3 years of MODIS retrievals from the Terra satellite and produce global and regional, seasonally varying, estimates of aerosol radiative effect over the clear-sky oceans.

  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. DEVELOPMENTS IN DIRECT THERMAL EXTRACTION GAS CHROMATOGRAPHY-MASS SPECTROMETRY OF FINE AEROSOLS

    EPA Science Inventory

    This examines thermal extraction gas chromatography-mass spectrometry (TE/GC/MS) applied to aerosols collected on filters. Several different TE/GC/MS systems as a group have speciated hundreds of individual organic constituents in ambient fine aerosols. Molecular marker source ap...

  10. Airborne measurements of spectral direct aerosol radiative forcing in INTEX/ICARTT (2004) and comparisons to previous campaigns

    NASA Astrophysics Data System (ADS)

    Redemann, J.; Pilewskie, P.; Russell, P.; Livingston, J.; Howard, S.; Schmid, B.; Pommier, J.; Gore, W.; Eilers, J.; Wendisch, M.; Bush, B.; Valero, F.

    2005-12-01

    As part of the INTEX-NA (INtercontinental chemical Transport EXperiment-North America) and ITCT (Intercontinental Transport and Chemical Transformation of anthropogenic pollution) field studies, the NASA Ames 14-channel Airborne Tracking Sunphotometer (AATS-14) and a pair of Solar Spectral Flux Radiometers (SSFR) took measurements from aboard a Jetstream 31 (J31) aircraft during 19 science flights (~ 53 flight hours) over the Gulf of Maine between 12 July and 8 August 2004. AATS-14 measures the direct solar beam transmission at 14 discrete wavelengths (354-2138 nm), yielding aerosol optical depth (AOD) spectra, while the SSFR system yields down- and upwelling solar irradiance at a spectral resolution of ~ 8-12 nm over the wavelength range 300-1700 nm. The combination of simultaneous AATS and SSFR measurements yields plots of net spectral irradiance as a function of aerosol optical depth as measured along horizontal flight legs. From the slope of these plots we determine the instantaneous aerosol-induced change in net radiative flux per change in AOD. By normalization to an aerosol optical depth change of unity we derive the spectral aerosol radiative forcing efficiency [W m-2 nm-1]. Numerical integration of the irradiance measurements over a given spectral range yields the broadband aerosol radiative forcing efficiency [W m-2]. In INTEX/ITCT, we observed a total of 16 horizontal AOD gradients, with 10 gradients well suited for our analysis because of the small changes in solar zenith angle. Within the 10 case studies we found a high variability in the derived instantaneous aerosol forcing efficiencies for the visible wavelength range (350-700 nm), with a mean of -79.6 W m-2 and a standard deviation of 21.8 W m-2 (27%). The mean instantaneous forcing efficiency for the visible plus near-IR wavelength range (350-1670 nm) was derived to be 135.3 W m-2 with a standard deviation of 36.0 W m-2 (27%). An analytical conversion of the instantaneous forcing efficiencies to

  11. A Sensitivity Study of Aerosol Effects on an Idealized Supercell Storm

    NASA Astrophysics Data System (ADS)

    Takeishi, A.; Storelvmo, T.

    2013-12-01

    One of the largest uncertainties in future climate projections lies in the climatic effects of aerosols. It has been shown that the cooling effect of aerosols could partially offset the current global warming induced by increased greenhouse gas concentration. Among the effects of aerosols, the interaction between aerosols and deep convective clouds is especially difficult to quantify, due to the complex interaction and limited measurements available. Although the radiative effect of deep convective clouds on climate is small, they could affect the local, regional, and global climate by altering precipitation and the large-scale circulations. Thus, it is of importance to understand how deep convection changes its development and evolution with aerosol loading. This study aims to understand the effects of varying aerosol number concentrations on deep convective clouds, using the Weather Research and Forecasting (WRF) model. A quarter-circular shear supercell is simulated with three different microphysics schemes in an idealized setting, while mimicking the changes in aerosol concentration by changing either cloud droplet concentration or activated cloud condensation nuclei concentration. We find that the simulated amount of precipitation has quite different sensitivities to aerosol concentration, depending on the microphysics scheme used; one of the simulations shows a drastic decrease in precipitation with increased aerosol loading, whereas simulations with the other two schemes show relatively low sensitivities to aerosol concentration. This fact highlights uncertainties in the complex microphysical interactions in convective clouds. In addition, changes in ice nuclei concentration are mimicked by changing the ice nucleation rate in each scheme. Sensitivity to this variation is also dependent on the microphysics scheme used. Furthermore, radiation is added in the simulations so that both radiative and microphysical effects of aerosol on the supercell storm are

  12. OMI tropospheric NO2 air mass factors over South America: effects of biomass burning aerosols

    NASA Astrophysics Data System (ADS)

    Castellanos, P.; Boersma, K. F.; Torres, O.; de Haan, J. F.

    2015-03-01

    Biomass burning is an important and uncertain source of aerosols and NOx (NO + NO2) to the atmosphere. OMI observations of tropospheric NO2 are essential for characterizing this emissions source, but inaccuracies in the retrieval of NO2 tropospheric columns due to the radiative effects of aerosols, especially light-absorbing carbonaceous aerosols, are not well understood. It has been shown that the O2-O2 effective cloud fraction and pressure retrieval is sensitive to aerosol optical and physical properties, including aerosol optical depth (AOD). Aerosols implicitly influence the tropospheric air mass factor (AMF) calculations used in the NO2 retrieval through the effective cloud parameters used in the independent pixel approximation. In this work, we explicitly account for the effects of biomass burning aerosols in the tropospheric NO2 AMF calculation by including collocated aerosol extinction vertical profile observations from the CALIOP instrument, and aerosol optical depth (AOD) and single scattering albedo (SSA) retrieved by the OMI near-UV aerosol algorithm (OMAERUV) in the DISAMAR radiative transfer model for cloud-free scenes. Tropospheric AMFs calculated with DISAMAR were benchmarked against AMFs reported in the Dutch OMI NO2 (DOMINO) retrieval; the mean and standard deviation (SD) of the difference was 0.6 ± 8%. Averaged over three successive South American biomass burning seasons (2006-2008), the spatial correlation in the 500 nm AOD retrieved by OMI and the 532 nm AOD retrieved by CALIOP was 0.6, and 72% of the daily OMAERUV AOD observations were within 0.3 of the CALIOP observations. Overall, tropospheric AMFs calculated with observed aerosol parameters were on average 10% higher than AMFs calculated with effective cloud parameters. For effective cloud radiance fractions less than 30%, or effective cloud pressures greater than 800 hPa, the difference between tropospheric AMFs based on implicit and explicit aerosol parameters is on average 6 and 3

  13. 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

  14. The Effects of Mineral Dust on the Hygroscopic and Optical Properties of Inorganic Salt Aerosols

    NASA Astrophysics Data System (ADS)

    Attwood, A. R.; Greenslade, M. E.

    2011-12-01

    Mineral dust particles are a significant fraction of the total aerosol mass, thus they play an important role in the Earth's radiative budget by direct scattering and absorption of radiation. Assessing this impact is complicated by the variability of optical properties resulting from water uptake and changes in chemical composition due to atmospheric mixing. Internal mixtures of montmorillonite, a clay component of mineral dust, with sodium chloride and ammonium sulfate were studied optically using cavity ring down spectroscopy. The effects of the addition of the clay to the optically observed deliquescence relative humidity (DRH) and water uptake of these salts was considered by investigating a series of different salt mass fractions. In most cases, montmorillonite alters the hygroscopic properties and causes the DRH to occur at a lower relative humidity. For ammonium sulfate, optical properties can be approximated by volume weighted mixing rules with some minor deviations around the DRH. For sodium chloride, this approximation is only accurate below the DRH with enhanced water uptake at higher relative humidities. Our results show