National Library of Energy BETA

Sample records for aerosols atmospheric profiling

  1. Toxicity of atmospheric aerosols on marine phytoplankton

    E-Print Network [OSTI]

    2009-01-01

    address: Center for Atmospheric Chemistry Study, Departmenttween phytoplankton, atmospheric chemistry, and climate areno. 12 ? 4601– 4605 CHEMISTRY Atmospheric aerosol deposition

  2. Composition and Reactions of Atmospheric Aerosol Particles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    Composition and Reactions of Atmospheric Aerosol Particles Print Microscopic aerosol particles in the atmosphere contain carbonaceous components from mineral dust and combustion...

  3. ARM: 10-minute Raman Lidar: aerosol extinction profiles and aerosol optical thickness, from first Ferrare algorithm

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Chitra Sivaraman; Connor Flynn

    1998-03-01

    10-minute Raman Lidar: aerosol extinction profiles and aerosol optical thickness, from first Ferrare algorithm

  4. ARM: 1-minute Raman Lidar: aerosol extinction profiles and aerosol optical thickness, from first Ferrare algorithm

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Chitra Sivaraman; Connor Flynn

    2004-10-01

    1-minute Raman Lidar: aerosol extinction profiles and aerosol optical thickness, from first Ferrare algorithm

  5. ARM: 10-minute Raman Lidar: aerosol extinction profiles and aerosol optical thickness, from first Ferrare algorithm

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Chitra Sivaraman; Connor Flynn

    10-minute Raman Lidar: aerosol extinction profiles and aerosol optical thickness, from first Ferrare algorithm

  6. ARM: 1-minute Raman Lidar: aerosol extinction profiles and aerosol optical thickness, from first Ferrare algorithm

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Chitra Sivaraman; Connor Flynn

    1-minute Raman Lidar: aerosol extinction profiles and aerosol optical thickness, from first Ferrare algorithm

  7. Composition and Reactions of Atmospheric Aerosol Particles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    on high-resolution scanning transmission x-ray images obtained at the ALS have revealed chemical reactions on and in atmospheric aerosol particles that caused particle growth...

  8. ARM: 10-minute TEMPORARY Raman Lidar: aerosol extinction profiles and aerosol optical thickness, from first Ferrare algorithm

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Sivaraman, Chitra; Flynn, Connor

    2010-12-15

    10-minute TEMPORARY Raman Lidar: aerosol extinction profiles and aerosol optical thickness, from first Ferrare algorithm

  9. ARM: 10-minute TEMPORARY Raman Lidar: aerosol extinction profiles and aerosol optical thickness, from first Ferrare algorithm

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Sivaraman, Chitra; Flynn, Connor

    10-minute TEMPORARY Raman Lidar: aerosol extinction profiles and aerosol optical thickness, from first Ferrare algorithm

  10. Atmospheric aerosol light scattering and polarization peculiarities

    E-Print Network [OSTI]

    Patlashenko, Zh I

    2015-01-01

    This paper considers environmental problems of natural and anthropogenic atmospheric aerosol pollution and its global and regional monitoring. Efficient aerosol investigations may be achieved by spectropolarimetric measurements. Specifically second and fourth Stokes parameters spectral dependencies carry information on averaged refraction and absorption indexes and on particles size distribution functions characteristics.

  11. Formation mechanisms and quantification of organic nitrates in atmospheric aerosol

    E-Print Network [OSTI]

    Rollins, Andrew Waite

    2010-01-01

    and J. Viidanoja, Atmospheric chemistry of c 3 -c 6organic nitrates, Atmospheric Chemistry and Physics, 9 (4),organic aerosol yields, Atmospheric Chemistry and Physics

  12. INTRODUCTION Atmospheric aerosol particles influence the Earth's

    E-Print Network [OSTI]

    Wunderle, Stefan

    , scattering, and absorbing solar electromagnetic radiation and by modifying cloud properties due to their roleINTRODUCTION Atmospheric aerosol particles influence the Earth's radiation budget by reflecting to maximum cover a region once in the daytime. In contrary, up-to-date geostationary instruments like

  13. The coupling of winds, aerosols and chemistry in Titan's atmosphere

    E-Print Network [OSTI]

    Hourdin, Chez Frédéric

    REVIEW The coupling of winds, aerosols and chemistry in Titan's atmosphere BY SEBASTIEN LEBONNOIS 1'Ae´ronomie, IPSL, CNRS, BP3, 91371 Verrie`res le Buisson, France The atmosphere of Titan is a complex system, where the observed atmospheric structure of Titan's lower atmosphere (mainly in the stratosphere and troposphere

  14. ARM: 10-minute Raman Lidar: aerosol scattering ratio and backscattering coefficient profiles, from first Ferrare algorithm

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Newsom, Rob; Goldsmith, John

    1998-03-01

    10-minute Raman Lidar: aerosol scattering ratio and backscattering coefficient profiles, from first Ferrare algorithm

  15. ARM: 1-minute Raman Lidar: aerosol scattering ratio and backscattering coefficient profiles, from first Ferrare algorithm

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Chitra Sivaraman; Connor Flynn

    2004-10-01

    1-minute Raman Lidar: aerosol scattering ratio and backscattering coefficient profiles, from first Ferrare algorithm

  16. ARM: 2-minute Raman Lidar: aerosol scattering ratio and backscattering coefficient profiles, from first Ferrare algorithm

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Sivaraman, Chitra; Flynn, Connor

    2004-10-01

    2-minute Raman Lidar: aerosol scattering ratio and backscattering coefficient profiles, from first Ferrare algorithm

  17. ARM: 10-second Raman Lidar: aerosol scattering ratio and backscattering coefficient profiles, from first Ferrare algorithm

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Chitra Sivaraman; Connor Flynn

    2004-10-01

    10-second Raman Lidar: aerosol scattering ratio and backscattering coefficient profiles, from first Ferrare algorithm

  18. ARM: 10-second Raman Lidar: aerosol scattering ratio and backscattering coefficient profiles, from first Ferrare algorithm

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Chitra Sivaraman; Connor Flynn

    10-second Raman Lidar: aerosol scattering ratio and backscattering coefficient profiles, from first Ferrare algorithm

  19. ARM: 10-minute Raman Lidar: aerosol scattering ratio and backscattering coefficient profiles, from first Ferrare algorithm

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Chitra Sivaraman; Connor Flynn

    10-minute Raman Lidar: aerosol scattering ratio and backscattering coefficient profiles, from first Ferrare algorithm

  20. ARM: 2-minute Raman Lidar: aerosol scattering ratio and backscattering coefficient profiles, from first Ferrare algorithm

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Sivaraman, Chitra; Flynn, Connor

    2-minute Raman Lidar: aerosol scattering ratio and backscattering coefficient profiles, from first Ferrare algorithm

  1. ARM: 1-minute Raman Lidar: aerosol scattering ratio and backscattering coefficient profiles, from first Ferrare algorithm

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Chitra Sivaraman; Connor Flynn

    1-minute Raman Lidar: aerosol scattering ratio and backscattering coefficient profiles, from first Ferrare algorithm

  2. Measurements of aerosol vertical profiles and optical properties during INDOEX

    E-Print Network [OSTI]

    , and the Kaashidhoo Climate Observatory (KCO) in the Maldives. Sun photometers were used to provide aerosol optical depths (AOD) needed to calibrate the MPL. This study focuses on the height distribution and optical trajectories, radiosonde profiles of temperature and humidity, and aerosol concentration and optical

  3. Composition and Reactions of Atmospheric Aerosol Particles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    they can have either cooling or warming effects. Lighter-colored organic carbon particles cool regions of the planet by scattering sunlight back into space. Other aerosol particles...

  4. Real time in situ detection of organic nitrates in atmospheric aerosols

    E-Print Network [OSTI]

    Rollins, Andrew W.

    2011-01-01

    +NO 3 reaction. Atmospheric Chemistry and Physics 2009, 9,radicals (NO 3 ). Atmospheric Chemistry and Physics 2008, 8,aerosol yields. Atmospheric Chemistry and Physics 2009, 9,

  5. Observations of Secondary Organic Aerosol Production and Soot Aging under Atmospheric Conditions Using a Novel Environmental Aerosol Chamber 

    E-Print Network [OSTI]

    Glen, Crystal

    2012-02-14

    of the processes leading to SOA production under ambient gaseous and particulate concentrations as well as the impact these aerosol types have on climate is poorly understood. Although the majority of atmospheric aerosols scatter radiation either directly...

  6. Profiling atmospheric aerosols | Argonne National Laboratory

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration wouldMass mapSpeedingProgramExemptions | NationalProcurementwork up forJackProbability

  7. Composition and Reactions of Atmospheric Aerosol Particles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    particles remain in the atmosphere can have a huge impact on the global climate. Measurements based on high-resolution scanning transmission x-ray images obtained at the ALS...

  8. Diesel Aerosol Sampling in the Atmosphere

    SciTech Connect (OSTI)

    David Kittelson; Jason Johnson; Winthrop Watts; Qiang Wei; Marcus Drayton; Dwane Paulsen; Nicolas Bukowiecki

    2000-06-19

    The University of Minnesota Center for Diesel Research along with a research team including Caterpillar, Cummins, Carnegie Mellon University, West Virginia University (WVU), Paul Scherrer Institute in Switzerland, and Tampere University in Finland have performed measurements of Diesel exhaust particle size distributions under real-world dilution conditions. A mobile aerosol emission laboratory (MEL) equipped to measure particle size distributions, number concentrations, surface area concentrations, particle bound PAHs, as well as CO 2 and NO x concentrations in real time was built and will be described. The MEL was used to follow two different Cummins powered tractors, one with an older engine (L10) and one with a state-of-the-art engine (ISM), on rural highways and measure particles in their exhaust plumes. This paper will describe the goals and objectives of the study and will describe representative particle size distributions observed in roadway experiments with the truck powered by the ISM engine.

  9. ARM: 10-minute TEMPORARY Raman Lidar: aerosol scattering ratio and backscattering coefficient profiles, from first Ferrare algorithm

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Sivaraman, Chitra; Flynn, Connor

    2010-12-15

    10-minute TEMPORARY Raman Lidar: aerosol scattering ratio and backscattering coefficient profiles, from first Ferrare algorithm

  10. ARM: 10-minute TEMPORARY Raman Lidar: aerosol scattering ratio and backscattering coefficient profiles, from first Ferrare algorithm

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Sivaraman, Chitra; Flynn, Connor

    10-minute TEMPORARY Raman Lidar: aerosol scattering ratio and backscattering coefficient profiles, from first Ferrare algorithm

  11. Unintended consequences of atmospheric injection of sulphate aerosols.

    SciTech Connect (OSTI)

    Brady, Patrick Vane; Kobos, Peter Holmes; Goldstein, Barry

    2010-10-01

    Most climate scientists believe that climate geoengineering is best considered as a potential complement to the mitigation of CO{sub 2} emissions, rather than as an alternative to it. Strong mitigation could achieve the equivalent of up to -4Wm{sup -2} radiative forcing on the century timescale, relative to a worst case scenario for rising CO{sub 2}. However, to tackle the remaining 3Wm{sup -2}, which are likely even in a best case scenario of strongly mitigated CO{sub 2} releases, a number of geoengineering options show promise. Injecting stratospheric aerosols is one of the least expensive and, potentially, most effective approaches and for that reason an examination of the possible unintended consequences of the implementation of atmospheric injections of sulphate aerosols was made. Chief among these are: reductions in rainfall, slowing of atmospheric ozone rebound, and differential changes in weather patterns. At the same time, there will be an increase in plant productivity. Lastly, because atmospheric sulphate injection would not mitigate ocean acidification, another side effect of fossil fuel burning, it would provide only a partial solution. Future research should aim at ameliorating the possible negative unintended consequences of atmospheric injections of sulphate injection. This might include modeling the optimum rate and particle type and size of aerosol injection, as well as the latitudinal, longitudinal and altitude of injection sites, to balance radiative forcing to decrease negative regional impacts. Similarly, future research might include modeling the optimum rate of decrease and location of injection sites to be closed to reduce or slow rapid warming upon aerosol injection cessation. A fruitful area for future research might be system modeling to enhance the possible positive increases in agricultural productivity. All such modeling must be supported by data collection and laboratory and field testing to enable iterative modeling to increase the accuracy and precision of the models, while reducing epistemic uncertainties.

  12. A VIBRATIONAL SPECTROSCOPIC STUDY OF AQUEOUS HYDROGEN HALIDE SOLUTIONS: APPLICATION TO ATMOSPHERIC AEROSOL CHEMISTRY

    E-Print Network [OSTI]

    Heterogeneous reactions on the surfaces of atmospheric aerosols play an important role in atmospheric chemistryA VIBRATIONAL SPECTROSCOPIC STUDY OF AQUEOUS HYDROGEN HALIDE SOLUTIONS: APPLICATION TO ATMOSPHERIC AEROSOL CHEMISTRY A Thesis Presented in Partial Fulfillment of the Requirements for the Degree Master

  13. Heterogeneous freezing of ice on atmospheric aerosols containing ash, soot, and soil

    E-Print Network [OSTI]

    Heterogeneous freezing of ice on atmospheric aerosols containing ash, soot, and soil Adam P. Fornea in the atmosphere often occurs through heterogeneous freezing processes in which an atmospheric aerosol acts, heterogeneous nucleation may occur through one of several freezing mechanisms, including contact and immersion

  14. Investigations of cloud altering effects of atmospheric aerosols using a new mixed Eulerian-Lagrangian aerosol model

    E-Print Network [OSTI]

    Steele, Henry Donnan, 1974-

    2004-01-01

    Industry, urban development, and other anthropogenic influences have substantially altered the composition and size-distribution of atmospheric aerosol particles over the last century. This, in turn, has altered cloud ...

  15. Atmospheric aerosols in Amazonia and land use change: from natural biogenic to biomass

    E-Print Network [OSTI]

    Atmospheric aerosols in Amazonia and land use change: from natural biogenic to biomass burning in Central Amazonia (TT34 North of Manaus) and at a heavily biomass burning impacted site in south-refractory PM1 aerosol loading at TT34, while biomass burning aerosols at PVH shows a 93% content of organic

  16. Radiative and thermodynamic responses to aerosol extinction profiles during the pre-monsoon month over South Asia

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Feng, Y.; Kotamarthi, V. R.; Coulter, R.; Zhao, C.; Cadeddu, M.

    2015-01-01

    Aerosol radiative effects and thermodynamic responses over South Asia are examined with a version of the Weather Research and Forecasting model coupled with Chemistry (WRF-Chem) for March 2012. Model results of Aerosol Optical Depth (AOD) and extinction profiles are analyzed and compared to satellite retrievals and two ground-based lidars located in the northern India. The WRF-Chem model is found to underestimate the AOD during the simulated pre-monsoon month and about 83 % of the model low-bias is due to aerosol extinctions below ~2 km. Doubling the calculated aerosol extinctions below 850 hPa generates much better agreement with the observed AODmore »and extinction profiles averaged over South Asia. To separate the effect of absorption and scattering properties, two runs were conducted: in one run (Case I), the calculated scattering and absorption coefficients were increased proportionally, while in the second run (Case II) only the calculated aerosol scattering coefficient was increased. With the same AOD and extinction profiles, the two runs produce significantly different radiative effects over land and oceans. On the regional mean basis, Case I generates 48 % more heating in the atmosphere and 21 % more dimming at the surface than Case II. Case I also produces stronger cooling responses over the land from the longwave radiation adjustment and boundary layer mixing. These rapid adjustments offset the stronger radiative heating in Case I and lead to an overall lower-troposphere cooling up to -0.7 K day?1, which is smaller than that in Case II. Over the ocean, direct radiative effects dominate the heating rate changes in the lower atmosphere lacking such surface and lower atmosphere adjustments due to fixed sea surface temperature, and the strongest atmospheric warming is obtained in Case I. Consequently, atmospheric dynamics (boundary layer heights and meridional circulation) and thermodynamic processes (water vapor and cloudiness) are shown to respond differently between Case I and Case II underlying the importance of determining the exact portion of scattering or absorbing aerosols that lead to the underestimation of aerosol optical depth in the model. In addition, the model results suggest that both direct radiative effect and rapid thermodynamic responses need to be quantified for understanding aerosol radiative impacts.« less

  17. Radiative and thermodynamic responses to aerosol extinction profiles during the pre-monsoon month over South Asia

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Feng, Y.; Kotamarthi, V. R.; Coulter, R.; Zhao, C.; Cadeddu, M.

    2015-06-19

    Aerosol radiative effects and thermodynamic responses over South Asia are examined with a version of the Weather Research and Forecasting model coupled with Chemistry (WRF-Chem) for March 2012. Model results of Aerosol Optical Depth (AOD) and extinction profiles are analyzed and compared to satellite retrievals and two ground-based lidars located in the northern India. The WRF-Chem model is found to underestimate the AOD during the simulated pre-monsoon month and about 83 % of the model low-bias is due to aerosol extinctions below ~2 km. Doubling the calculated aerosol extinctions below 850 hPa generates much better agreement with the observed AODmore »and extinction profiles averaged over South Asia. To separate the effect of absorption and scattering properties, two runs were conducted: in one run (Case I), the calculated scattering and absorption coefficients were increased proportionally, while in the second run (Case II) only the calculated aerosol scattering coefficient was increased. With the same AOD and extinction profiles, the two runs produce significantly different radiative effects over land and oceans. On the regional mean basis, Case I generates 48 % more heating in the atmosphere and 21 % more dimming at the surface than Case II. Case I also produces stronger cooling responses over the land from the longwave radiation adjustment and boundary layer mixing. These rapid adjustments offset the stronger radiative heating in Case I and lead to an overall lower-troposphere cooling up to -0.7 K day?1, which is smaller than that in Case II. Over the ocean, direct radiative effects dominate the heating rate changes in the lower atmosphere lacking such surface and lower atmosphere adjustments due to fixed sea surface temperature, and the strongest atmospheric warming is obtained in Case I. Consequently, atmospheric dynamics (boundary layer heights and meridional circulation) and thermodynamic processes (water vapor and cloudiness) are shown to respond differently between Case I and Case II underlying the importance of determining the exact portion of scattering or absorbing aerosols that lead to the underestimation of aerosol optical depth in the model. In addition, the model results suggest that both direct radiative effect and rapid thermodynamic responses need to be quantified for understanding aerosol radiative impacts.« less

  18. The aging of organic aerosol in the atmosphere : chemical transformations by heterogeneous oxidation

    E-Print Network [OSTI]

    Kessler, Sean Herbert

    2013-01-01

    The immense chemical complexity of atmospheric organic particulate matter ("aerosol") has left the general field of condensed-phase atmospheric organic chemistry relatively under-developed when compared with either gas-phase ...

  19. Investigating the Impacts of Atmospheric Aerosols on Cloud Formation Relevant to Weather and Climate 

    E-Print Network [OSTI]

    Mckeown, Megan Alexandra

    2014-12-10

    on weather, climate, visibility, air quality, and human health. In this project, the impacts of aerosols on cloud formation potential in the atmosphere have been assessed using several laboratory experimental approaches. To study the effects of atmospheric...

  20. The impact of atmospheric aerosols on trace metal chemistry in open ocean surface seawater 3. Lead

    SciTech Connect (OSTI)

    Maring, H.B.; Duce, R.A. )

    1990-04-15

    Atmospheric aerosols collected at Enewetak Atoll in the tropical North Pacific were exposed to seawater in laboratory experiments to assess the impact of atmospheric aerosols on lead chemistry in surface seawater. The net atmospheric flux of soluble lead to the ocean is between 16 and 32 pmol cm{sup {minus}2}/yr at Enewetak. The stable lead isotopic composition of soluble aerosol lead indicates that it is of anthropogenic origin. Anthropogenic aerosol lead from Central and North America appears to be less soluble and/or to dissolve less rapidly than that from Asia. Dissolved organic matter and possibly lower pH appear to increase the nonaluminosilicate aerosol lead solubility and/or dissolution rate. The isotopic composition of lead in air, seawater and dry deposition suggests that after deposition in the ocean, nonaluminosilicate particulate lead can be reinjected into the atmosphere during sea salt aerosol production.

  1. ARM: 10-minute Raman Lidar: aerosol depolarization profiles and single layer cloud optical depths from first Turner algorithm

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Chitra Sivaraman; Connor Flynn

    1998-03-01

    10-minute Raman Lidar: aerosol depolarization profiles and single layer cloud optical depths from first Turner algorithm

  2. ARM: 10-minute Raman Lidar: aerosol depolarization profiles and single layer cloud optical depths from first Turner algorithm

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Chitra Sivaraman; Connor Flynn

    10-minute Raman Lidar: aerosol depolarization profiles and single layer cloud optical depths from first Turner algorithm

  3. Atmospheric Environment 41 (2007) 73897400 Fire and biofuel contributions to annual mean aerosol mass

    E-Print Network [OSTI]

    Jacob, Daniel J.

    2007-01-01

    Atmospheric Environment 41 (2007) 7389­7400 Fire and biofuel contributions to annual mean aerosol estimate the contributions from biomass burning (summer wildfires, other fires, residential biofuel, and industrial biofuel) to seasonal and annual aerosol concentrations in the United States. Our approach

  4. Chemistry of carbonaceous aerosols : studies of atmospheric processing and OH-initiated oxidation

    E-Print Network [OSTI]

    Johnson, Kirsten S. (Kirsten Sue)

    2008-01-01

    Carbonaceous aerosols are among the most prevalent yet least understood constituents of the atmosphere, particularly in urban environments. We have performed analyses of field samples and laboratory studies to probe the ...

  5. Light Scattering by Ice Crystals and Mineral Dust Aerosols in the Atmosphere 

    E-Print Network [OSTI]

    Bi, Lei

    2012-07-16

    Modeling the single-scattering properties of nonspherical particles in the atmo¬sphere (in particular, ice crystals and dust aerosols) has important applications to climate and remote sensing studies. The ?rst part of the dissertation (Chapters II...

  6. Constraining the atmospheric composition of the day-night terminators of HD 189733b: Atmospheric retrieval with aerosols

    SciTech Connect (OSTI)

    Lee, Jae-Min; Irwin, Patrick G. J.; Fletcher, Leigh N.; Barstow, Joanna K.; Heng, Kevin

    2014-07-01

    A number of observations have shown that Rayleigh scattering by aerosols dominates the transmission spectrum of HD 189733b at wavelengths shortward of 1 ?m. In this study, we retrieve a range of aerosol distributions consistent with transmission spectroscopy between 0.3-24 ?m that were recently re-analyzed by Pont et al. To constrain the particle size and the optical depth of the aerosol layer, we investigate the degeneracies between aerosol composition, temperature, planetary radius, and molecular abundances that prevent unique solutions for transit spectroscopy. Assuming that the aerosol is composed of MgSiO{sub 3}, we suggest that a vertically uniform aerosol layer over all pressures with a monodisperse particle size smaller than about 0.1 ?m and an optical depth in the range 0.002-0.02 at 1 ?m provides statistically meaningful solutions for the day/night terminator regions of HD 189733b. Generally, we find that a uniform aerosol layer provide adequate fits to the data if the optical depth is less than 0.1 and the particle size is smaller than 0.1 ?m, irrespective of the atmospheric temperature, planetary radius, aerosol composition, and gaseous molecules. Strong constraints on the aerosol properties are provided by spectra at wavelengths shortward of 1 ?m as well as longward of 8 ?m, if the aerosol material has absorption features in this region. We show that these are the optimal wavelengths for quantifying the effects of aerosols, which may guide the design of future space observations. The present investigation indicates that the current data offer sufficient information to constrain some of the aerosol properties of HD189733b, but the chemistry in the terminator regions remains uncertain.

  7. Simulation of Aerosol Behavior in a Saturated Atmosphere With the CONTAIN Code

    SciTech Connect (OSTI)

    Kljenak, Ivo; Mavko, Borut [Jozef Stefan Institute, Jamova cesta 39, 1000 Ljubljana (Slovenia)

    2002-07-01

    Experiments on aerosol behavior in an atmosphere containing saturated vapor, which were performed in the KAEVER experimental facility and proposed for the OECD International Standard Problem No. 44, were simulated with the CONTAIN thermal-hydraulic computer code. The purpose of the work was to assess the capability of the CONTAIN code to model aerosol condensation and deposition in a containment of a light-water-reactor nuclear power plant at severe accident conditions. Results of dry and wet aerosol concentrations in the test vessel atmosphere are presented and analyzed. (authors)

  8. The impact of natural versus anthropogenic aerosols on atmospheric circulation in the Community

    E-Print Network [OSTI]

    Sherwood, Steven

    The impact of natural versus anthropogenic aerosols on atmospheric circulation in the Community strengthen wintertime zonal wind near 60°N, weaken it near 30°N, warm the tropo- sphere, cool and absorb solar radiation, and therefore contribute to atmospheric solar heating and surface cooling (Ramana

  9. Aerosol specification in single-column Community Atmosphere Model version 5

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Lebassi-Habtezion, B.; Caldwell, P. M.

    2015-03-27

    Single-column model (SCM) capability is an important tool for general circulation model development. In this study, the SCM mode of version 5 of the Community Atmosphere Model (CAM5) is shown to handle aerosol initialization and advection improperly, resulting in aerosol, cloud-droplet, and ice crystal concentrations which are typically much lower than observed or simulated by CAM5 in global mode. This deficiency has a major impact on stratiform cloud simulations but has little impact on convective case studies because aerosol is currently not used by CAM5 convective schemes and convective cases are typically longer in duration (so initialization is less important).more »By imposing fixed aerosol or cloud-droplet and crystal number concentrations, the aerosol issues described above can be avoided. Sensitivity studies using these idealizations suggest that the Meyers et al. (1992) ice nucleation scheme prevents mixed-phase cloud from existing by producing too many ice crystals. Microphysics is shown to strongly deplete cloud water in stratiform cases, indicating problems with sequential splitting in CAM5 and the need for careful interpretation of output from sequentially split climate models. Droplet concentration in the general circulation model (GCM) version of CAM5 is also shown to be far too low (~ 25 cm?3) at the southern Great Plains (SGP) Atmospheric Radiation Measurement (ARM) site.« less

  10. ATMOSPHERIC AEROSOL RESEARCH, ANNUAL REPORT 1976-77

    E-Print Network [OSTI]

    Novakov, T.

    2010-01-01

    Atmospheric Chemistry Catalytic Oxidation of ,S02 on Carbonand S.G. Chang, "Catalytic oxidation of S02 on carbonCHEMISTRY LBL-6819 Catalytic Oxidation of S02 on Carbon in

  11. Laboratory Studies of Processing of Carbonaceous Aerosols by Atmospheric Oxidants/Hygroscopicity and CCN Activity of Secondary & Processed Primary Organic Aerosols

    SciTech Connect (OSTI)

    Ziemann, P.J.; Arey, J.; Atkinson, R.; Kreidenweis, S.M.; Petters, M.D.

    2012-06-13

    The atmosphere is composed of a complex mixture of gases and suspended microscopic aerosol particles. The ability of these particles to take up water (hygroscopicity) and to act as nuclei for cloud droplet formation significantly impacts aerosol light scattering and absorption, and cloud formation, thereby influencing air quality, visibility, and climate in important ways. A substantial, yet poorly characterized component of the atmospheric aerosol is organic matter. Its major sources are direct emissions from combustion processes, which are referred to as primary organic aerosol (POA), or in situ processes in which volatile organic compounds (VOCs) are oxidized in the atmosphere to low volatility reaction products that subsequent condense to form particles that are referred to as secondary organic aerosol (SOA). POA and VOCs are emitted to the atmosphere from both anthropogenic and natural (biogenic) sources. The overall goal of this experimental research project was to conduct laboratory studies under simulated atmospheric conditions to investigate the effects of the chemical composition of organic aerosol particles on their hygroscopicity and cloud condensation nucleation (CCN) activity, in order to develop quantitative relationships that could be used to more accurately incorporate aerosol-cloud interactions into regional and global atmospheric models. More specifically, the project aimed to determine the products, mechanisms, and rates of chemical reactions involved in the processing of organic aerosol particles by atmospheric oxidants and to investigate the relationships between the chemical composition of organic particles (as represented by molecule sizes and the specific functional groups that are present) and the hygroscopicity and CCN activity of oxidized POA and SOA formed from the oxidation of the major classes of anthropogenic and biogenic VOCs that are emitted to the atmosphere, as well as model hydrocarbons. The general approach for this project was to carry out reactions of representative anthropogenic and biogenic VOCs and organic particles with ozone (O3), and hydroxyl (OH), nitrate (NO3), and chlorine (Cl) radicals, which are the major atmospheric oxidants, under simulated atmospheric conditions in large-volume environmental chambers. A combination of on-line and off-line analytical techniques were used to monitor the chemical and physical properties of the particles including their hygroscopicity and CCN activity. The results of the studies were used to (1) improve scientific understanding of the relationships between the chemical composition of organic particles and their hygroscopicity and CCN activity, (2) develop an improved molecular level theoretical framework for describing these relationships, and (3) establish a large database that is being used to develop parameterizations relating organic aerosol chemical properties and SOA sources to particle hygroscopicity and CCN activity for use in regional and global atmospheric air quality and climate models.

  12. Scale-free Universal Spectrum for Atmospheric Aerosol Size Distribution for Davos, Mauna Loa and Izana

    E-Print Network [OSTI]

    A. M. Selvam

    2014-08-14

    Atmospheric flows exhibit fractal fluctuations and inverse power law form for power spectra indicating an eddy continuum structure for the selfsimilar fluctuations. A general systems theory for fractal fluctuations developed by the author is based on the simple visualisation that large eddies form by space-time integration of enclosed turbulent eddies, a concept analogous to Kinetic Theory of Gases in Classical Statistical Physics. The ordered growth of atmospheric eddy continuum is in dynamical equilibrium and is associated with Maximum Entropy Production. The model predicts universal (scale-free) inverse power law form for fractal fluctuations expressed in terms of the golden mean. Atmospheric particulates are held in suspension in the fractal fluctuations of vertical wind velocity. The mass or radius (size) distribution for homogeneous suspended atmospheric particulates is expressed as a universal scale-independent function of the golden mean, the total number concentration and the mean volume radius. Model predicted spectrum is in agreement (within two standard deviations on either side of the mean) with total averaged radius size spectra for the AERONET (aerosol inversions) stations Davos and Mauna Loa for the year 2010 and Izana for the year 2009 daily averages. The general systems theory model for aerosol size distribution is scale free and is derived directly from atmospheric eddy dynamical concepts. At present empirical models such as the log normal distribution with arbitrary constants for the size distribution of atmospheric suspended particulates are used for quantitative estimation of earth-atmosphere radiation budget related to climate warming/cooling trends. The universal aerosol size spectrum will have applications in computations of radiation balance of earth-atmosphere system in climate models.

  13. Nuclear Emergency and the Atmospheric Dispersion of Nuclear Aerosols: Discussion of the Shared Nuclear Future - 13163

    SciTech Connect (OSTI)

    Rana, Mukhtar A. [Science-Admin Coherence Cell (SACC), PINSTECH Admin Blk, PAEC, Islamabad (Pakistan)] [Science-Admin Coherence Cell (SACC), PINSTECH Admin Blk, PAEC, Islamabad (Pakistan); Ali, Nawab [Physics Division, Directorate of Science, Pakistan Institute of Nuclear Science and Technology (PINSTECH), P.O. Nilore, Islamabad (Pakistan)] [Physics Division, Directorate of Science, Pakistan Institute of Nuclear Science and Technology (PINSTECH), P.O. Nilore, Islamabad (Pakistan); Akhter, Parveen [Pakistan Institute of Engineering and Applied Sciences (PIEAS), Islamabad (Pakistan)] [Pakistan Institute of Engineering and Applied Sciences (PIEAS), Islamabad (Pakistan); Khan, E.U. [Department of Physics, International Islamic University (IIU), Kettle Fields, Kashmir Highways, Islamabad (Pakistan)] [Department of Physics, International Islamic University (IIU), Kettle Fields, Kashmir Highways, Islamabad (Pakistan); Mathieson, John [International Relations, Nuclear Decommissioning Authority (NDA), Building 587, Curie Avenue, Harwell, Didcot, Oxon, OX11 0RH (United Kingdom)] [International Relations, Nuclear Decommissioning Authority (NDA), Building 587, Curie Avenue, Harwell, Didcot, Oxon, OX11 0RH (United Kingdom)

    2013-07-01

    This paper has a twofold objective. One is to analyze the current status of high-level nuclear waste disposal along with presentation of practical perspectives about the environmental issues involved. Present disposal designs and concepts are analyzed on a scientific basis and modifications to existing designs are proposed from the perspective of environmental safety. Other is to understand the aerosol formation in the atmosphere for the case of the leakage from the nuclear waste containers or a nuclear accident. Radio-nuclides released from the waste will attach themselves to the existing aerosols in the atmosphere along with formation of new aerosols. Anticipating the nuclear accident when a variety of radioactive aerosols will form and exist in the atmosphere, as a simple example, measurement of naturally existing radioactive aerosols are made in the atmosphere of Islamabad and Murree. A comparison with similar measurements in 3 cities of France is provided. Measurement of radionuclides in the atmosphere, their attachment to aerosols and follow up transport mechanisms are key issues in the nuclear safety. It is studied here how {sup 7}Be concentration in the atmospheric air varies in the capital city of Islamabad and a Himalaya foothill city of Murree (Pakistan). Present results are compared with recent related published results to produce a {sup 7}Be concentration versus altitude plot up to an altitude of 4000 m (a.s.l.). Origin and variance of {sup 7}Be concentration at different altitudes is discussed in detail. The relevance of results presented here with the evaluation of implications of Chernobyl and Fukushima nuclear disasters has been discussed in a conclusive manner. It is the first international report of a joint collaboration/project. The project is being generalized to investigate and formulate a smooth waste storage and disposal policy. The project will address the fission and fusion waste reduction, its storage, its recycling, air, water and soil quality monitoring, and the final disposal with the major foci of dealing with related chemical, biogical, physical, geophysical, engineering, management and administration aspects. (authors)

  14. Sampling, characterization, and remote sensing of aerosols formed in the atmospheric hydrolysis of uranium hexafluoride

    SciTech Connect (OSTI)

    Bostick, W.D.; McCulla, W.H.; Pickrell, P.W.

    1984-05-01

    When gaseous uranium hexafluoride (UF/sub 6/) is released into the atmosphere, it rapidly reacts with ambient moisture to form an aerosol of uranyl fluoride (UO/sub 2/F/sub 2/) and hydrogen fluoride (HF). As part of our Safety Analysis program, we have performed several experimental releases of HF/sub 6/ in contained volumes in order to investigate techniques for sampling and characterizing the aerosol materials. The aggregate particle morphology and size distribution have been found to be dependent upon several conditions, including the temperature of the UF/sub 6/ at the time of its release, the relative humidity of the air into which it is released, and the elapsed time after the release. Aerosol composition and settling rate have been investigated using stationary samplers for the separate collection of UO/sub 2/F/sub 2/ and HF and via laser spectroscopic remote sensing (Mie scatter and infrared spectroscopy). 25 refs., 16 figs., 5 tabs.

  15. Sampling and characterization of aerosols formed in the atmospheric hydrolysis of UF/sub 6/

    SciTech Connect (OSTI)

    Bostick, W.D.; McCulla, W.H.; Pickrell, P.W.; Branam, D.A.

    1983-01-01

    When gaseous UF/sub 6/ is released into the atmosphere, it rapidly reacts with ambient moisture to form an aerosol of uranyl fluoride and HF. As part of our Safety Analysis program, we have performed several experimental releases of UF/sub 6/ (from natural uranium) in contained volumes in order to investigate techniques for sampling and characterizing the aerosol materials. The aggregrate particle morphology and size distribution have been found to be dependent upon several conditions, including the relative humidity at the time of the release and the elapse time after the release. Aerosol composition and settling rate have been investigated using isokinetic samplers for the separate collection of UO/sub 2/F/sub 2/ and HF, and via laser spectroscopic remote sensing (Mie scatter and infrared spectroscopy). 8 references.

  16. Program Abstracts: Formation and Growth of Atmospheric Aerosols

    SciTech Connect (OSTI)

    Peter H. McMurry; Markku Kulmala

    2006-09-07

    DOE provided $11,000 to sponsor the Workshop on New Particle Formation in the Atmosphere, which was held at The Riverwood Inn and Conference Center near Minneapolis, MN from September 7 to 9, 2006. Recent work has shown that new particle formation is an important atmospheric process that must be better understood due to its impact on cloud cover and the Earth's radiation balance. The conference was an informal gathering of atmospheric and basic scientists with expertise pertinent to this topic. The workshop included discussions of: • atmospheric modeling; • computational chemistry pertinent to clustering; • ions and ion induced nucleation; • basic laboratory and theoretical studies of nucleation; • studies on neutral molecular clusters; • interactions of organic compounds and sulfuric acid; • composition of freshly nucleated particles. Fifty six scientists attended the conference. They included 27 senior scientists, 9 younger independent scientists (assistant professor or young associate professor level), 7 postdocs, 13 graduate students, 10 women, 35 North Americans (34 from the U.S.), 1 Asian, and 20 Europeans. This was an excellent informal workshop on an important topic. An effort was made to include individuals from communities that do not regularly interact. A number of participants have provided informal feedback indicating that the workshop led to research ideas and possible future collaborations.

  17. Typical atmospheric aerosol behavior at the Cherenkov Telescope Array candidate sites in Argentina

    E-Print Network [OSTI]

    Piacentini, Rubén D; Micheletti, María I; Salum, Graciela M; Maya, Javier; Mancilla, Alexis; García, Beatriz

    2013-01-01

    Aerosols from natural and antropogenic sources are one of the atmospheric components that have the largest spacial-temporal variability, depending on the type (land or ocean) surface, human activity and climatic conditions (mainly temperature and wind). Since Cherenkov photons generated by the incidence of a primary ultraenergetic cosmic gamma photon have a spectral intensity distribution concentrated in the UV and visible ranges [Hillas AM. Space Science Reviews, 75, 17-30, 1996], it is important to know the aerosol concentration and its contribution to atmospheric radiative transfer. We present results of this concentration measured in typical rather calm (not windy) days at San Antonio de los Cobres (SAC) and El Leoncito/CASLEO proposed Argentinean Andes range sites for the placement of the Cherenkov Telescope Array (CTA). In both places, the aerosol concentration has a peak in the 2.5-5.0$\\mu$m range of the mean aerosol diameter and a very low mean total concentration of 0.097$\\mu$g/m$^3$ (0.365$\\mu$g/m$^...

  18. Assessing the Influence of Secondary Organic versus Primary Carbonaceous Aerosols on Long-Range Atmospheric Polycyclic Aromatic Hydrocarbon Transport

    E-Print Network [OSTI]

    Pierce, J. R.

    We use the chemical transport model GEOS-Chem to evaluate the hypothesis that atmospheric polycyclic aromatic hydrocarbons (PAHs) are trapped in secondary organic aerosol (SOA) as it forms. We test the ability of three ...

  19. Nonlinear Effects of Coexisting Surface and Atmospheric Forcing of Anthropogenic Absorbing Aerosols: Impact on the South Asian Monsoon Onset

    E-Print Network [OSTI]

    Lee, Shao-Yi

    The direct radiative effect of absorbing aerosols consists of absorption-induced atmospheric heating together with scattering- and absorption-induced surface cooling. It is thus important to understand whether some of the ...

  20. Non-linear photochemical pathways in laser induced atmospheric aerosol formation

    E-Print Network [OSTI]

    Mongin, Denis; Schubert, Elise; Brisset, Jean-Gabriel; Berti, Nicolas; Moret, Michel; Prévôt, André S H; Baltensperger, Urs; Kasparian, Jérôme; Wolf, Jean-Pierre

    2015-01-01

    We measured the chemical composition and the size distribution of aerosols generated by femtosecond-Terawatt laser pulses in the atmosphere using an aerosol mass spectrometer (AMS). We show that nitric acid condenses in the form of ammonium nitrate, and that oxidized volatile organics also contribute to particle growth. These two components account for two thirds and one third, respectively, of the dry laser-condensed mass. They appear in two different modes centred at 380 nm and 150 nm. The number concentration of particles between 25 and 300 nm increases by a factor of 15. Pre-existing water droplets strongly increase the oxidative properties of the laser-activated atmosphere, substantially enhancing the condensation of organics under laser illumination.

  1. Climatological simulations of ozone and atmospheric aerosols in the Greater Cairo region

    SciTech Connect (OSTI)

    Steiner, A. L.; Tawfik, A. B.; Shalaby, A.; Zakey, A. S.; Abdel Wahab, M. M.; Salah, Z.; Solmon, F.; Sillman, S.; Zaveri, Rahul A.

    2014-04-16

    An integrated chemistry-climate model (RegCM4-CHEM) simulates present-day climate, ozone and tropospheric aerosols over Egypt with a focus on Greater Cairo (GC) region. The densley populated GC region is known for its severe air quality issues driven by high levels of anthropogenic pollution in conjuction with natural sources such as dust and agricultural burning events. We find that current global emission inventories underestimate key pollutants such as nitrogen oxides and anthropogenic aerosol species. In the GC region, average-ground-based NO2 observations of 40-60 ppb are substantially higher than modeled estimates (5-10 ppb), likely due to model grid resolution, improper boundary layer representation, and poor emissions inventories. Observed ozone concentrations range from 35 ppb (winter) to 80 ppb (summer). The model reproduces the seasonal cycle fairly well, but modeled summer ozone is understimated by approximately 15 ppb and exhibits little interannual variability. For aerosols, springtime dust events dominate the seasonal aerosol cycle. The chemistry-climate model captures the springtime peak aerosol optical depth (AOD) of 0.7-1 but is slightly greater than satellite-derived AOD. Observed AOD decreases in the summer and increases again in the fall due to agricultural burning events in the Nile Delta, yet the model underestimates this fall observed AOD peak, as standard emissions inventories underestimate this burning and the resulting aerosol emissions. Our comparison of modeled gas and particulate phase atmospheric chemistry in the GC region indicates that improved emissions inventories of mobile sources and other anthropogenic activities are needed to improve air quality simulations in this region.

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

    SciTech Connect (OSTI)

    Keene, William C.; Long, Michael S.

    2013-05-20

    This project examined the potential large-scale influence of marine aerosol cycling on atmospheric chemistry, physics and radiative transfer. Measurements indicate that the size-dependent generation of marine aerosols by wind waves at the ocean surface and the subsequent production and cycling of halogen-radicals are important but poorly constrained processes that influence climate regionally and globally. A reliable capacity to examine the role of marine aerosol in the global-scale atmospheric system requires that the important size-resolved chemical processes be treated explicitly. But the treatment of multiphase chemistry across the breadth of chemical scenarios encountered throughout the atmosphere is sensitive to the initial conditions and the precision of the solution method. This study examined this sensitivity, constrained it using high-resolution laboratory and field measurements, and deployed it in a coupled chemical-microphysical 3-D atmosphere model. First, laboratory measurements of fresh, unreacted marine aerosol were used to formulate a sea-state based marine aerosol source parameterization that captured the initial organic, inorganic, and physical conditions of the aerosol population. Second, a multiphase chemical mechanism, solved using the Max Planck Institute for Chemistryâ??s MECCA (Module Efficiently Calculating the Chemistry of the Atmosphere) system, was benchmarked across a broad set of observed chemical and physical conditions in the marine atmosphere. Using these results, the mechanism was systematically reduced to maximize computational speed. Finally, the mechanism was coupled to the 3-mode modal aerosol version of the NCAR Community Atmosphere Model (CAM v3.6.33). Decadal-scale simulations with CAM v.3.6.33, were run both with and without reactive-halogen chemistry and with and without explicit treatment of particulate organic carbon in the marine aerosol source function. Simulated results were interpreted (1) to evaluate influences of marine aerosol production on the microphysical properties of aerosol populations and clouds over the ocean and the corresponding direct and indirect effects on radiative transfer; (2) atmospheric burdens of reactive halogen species and their impacts on O3, NOx, OH, DMS, and particulate non-sea-salt SO42-; and (3) the global production and influences of marine-derived particulate organic carbon. The model reproduced major characteristics of the marine aerosol system and demonstrated the potential sensitivity of global, decadal-scale climate metrics to multiphase marine-derived components of Earthâ??s troposphere. Due to the combined computational burden of the coupled system, the currently available computational resources were the limiting factor preventing the adequate statistical analysis of the overall impact that multiphase chemistry might have on climate-scale radiative transfer and climate.

  3. Change in atmospheric mineral aerosols in response to climate: Last glacial period, preindustrial, modern, and doubled carbon dioxide

    E-Print Network [OSTI]

    Mahowald, Natalie

    Change in atmospheric mineral aerosols in response to climate: Last glacial period, preindustrial generated by the National Center for Atmospheric Research's Community Climate System Model for the current climate are shown to be consistent with present day satellite and deposition data. The response

  4. Atmospheric Radiation Measurement (ARM) Data from Point Reyes, California for the Marine Stratus, Radiation, Aerosol, and Drizzle (MASRAD) Project

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Point Reyes National Seashore, on the California coast north of San Francisco, was the location of the first deployment of the DOE's Atmospheric Radiation Measurement (ARM) Mobile Facility (AMF). The ARM Program collaborated with the U.S. Office of Naval Research and DOE's Aerosol Science Program in the Marine Stratus, Radiation, Aerosol, and Drizzle (MASRAD) project. Their objectives were to collect data from cloud/aerosol interactions and to improve understanding of cloud organization that is often associated with patches of drizzle. Between March and September 2005, the AMF and at least two research aircraft were used to collect data.

  5. Atmospheric Radiation Measurment (ARM) Data from the Ganges Valley, India for the Ganges Valley Aerosol Experiment (GVAX)

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    In 2011 and 2012, the Ganges Valley Aerosol Experiment (GVAX) began in the Ganges Valley region of India. The objective was to obtain measurements of clouds, precipitation, and complex aerosols to study their impact on cloud formation and monsoon activity in the region. During the Indian Ocean Experiment (INDOEX) field studies, aerosols from the Ganges Valley region were shown to affect cloud formation and monsoon activity over the Indian Ocean. The complex field study used the ARM Mobile Facility (AMF) to measure radiative, cloud, convection, and aerosol characteristics over the mainland. The resulting data set captured pre-monsoon to post-monsoon conditions to establish a comprehensive baseline for advancements in the study of the effects of atmospheric conditions of the Ganges Valley.

  6. Surface Electric Fields of Aqueous Solutions of NH4NO3, Mg(NO3)2, NaNO3, and LiNO3: Implications for Atmospheric Aerosol Chemistry

    E-Print Network [OSTI]

    for Atmospheric Aerosol Chemistry Wei Hua, Dominique Verreault, and Heather C. Allen* Department of Chemistry aerosol processes and potential impact on atmospheric chemistry. However, there is sparse surface data heterogeneous chemistry of atmospheric aerosols.1-7 Yet, surface propensity, or surface activity, of ions

  7. UNDERSTANDING THE INFLUENCES OF ATMOSPHERIC AEROSOLS ON CLIMATE AND CLIMATE CHANGE

    E-Print Network [OSTI]

    Schwartz, Stephen E.

    remarks #12;DMS #12;AEROSOL IN MEXICO CITY BASIN #12;AEROSOL IN MEXICO CITY BASIN Light scattering by aerosols decreases absorption of solar radiation. #12;AEROSOLS AS SEEN FROM SPACE Fire plumes from southern Mexico transported north into Gulf of Mexico. #12;CLOUD BRIGHTENING BY SHIP TRACKS Satellite photo off

  8. Data quality monitoring in the presence of aerosols and other adverse atmospheric conditions with H.E.S.S

    E-Print Network [OSTI]

    Hahn, J; Bernlöhr, K; Krüger, P; Lo, Y T E; Chadwick, P M; Daniel, M K; Deil, C; Gast, H; Kosack, K; Marandon, V

    2015-01-01

    Cherenkov telescope experiments, such as H.E.S.S., have been very successful in astronomical observations in the very-high-energy (VHE; E $>$ 100 GeV) regime. As an integral part of the detector, such experiments use Earth's atmosphere as a calorimeter. For the calibration and energy determination, a standard model atmosphere is assumed. Deviations of the real atmosphere from the model may therefore lead to an energy misreconstruction of primary gamma rays. To guarantee satisfactory data quality with respect to difficult atmospheric conditions, several atmospheric data quality criteria are implemented in the H.E.S.S. software. These quantities are sensitive to clouds and aerosols. Here, the Cherenkov transparency coefficient will be presented. It is a new monitoring quantity that is able to measure long-term changes in the atmospheric transparency. The Cherenkov transparency coefficient derives exclusively from Cherenkov data and is quite hardware-independent. Furthermore, its positive correlation with indepe...

  9. Atmospheric Radiation Measurement (ARM) Data from Shouxian, China for the Study of Aerosol Indirect Effects in China

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    In a complex ARM Mobile Facility (AMF) deployment, monitoring data was collected at four locations in China during 2008. The various sites are located in regions with different climate regimes and with high aerosol loadings of different optical, physical, and chemical properties. Measurements obtained at all the AMF sites during the 8-month deployment in China will help scientists to validate satellite-based findings, understand the mechanisms of the aerosol indirect effects in the region, and examine the roles of aerosols in affecting regional climate and atmospheric circulation, with a special focus on the impact of the East Asian monsoon system. As with other collections from the ARM Mobile Facility, the datasets are available from the ARM Archive. The ARM Archive physically resides at the Oak Ridge National Laboratory.

  10. Retrieval of cloud-cleared atmospheric temperature profiles from hyperspectral infrared and microwave observations

    E-Print Network [OSTI]

    Blackwell, William Joseph, 1971-

    2002-01-01

    This thesis addresses the problem of retrieving the temperature profile of the Earth's atmosphere from overhead infrared and microwave observations of spectral radiance in cloudy conditions. The contributions of the thesis ...

  11. El Roque de Los Muchachos Site Characteristics. III. Analysis of Atmospheric Dust and Aerosol Extinction

    E-Print Network [OSTI]

    Lombardi, G; Ortolani, S; Pedani, M; Ghedina, A

    2008-01-01

    Canary Islands are normally interested by dominant North-East winds that, in some meteorological conditions, can transport sand at high altitude from the Sahara desert. The dust may affect the efficiency of the telescopes and decreases the transparency of the sky. In order to maximize the scientific return of the telescopes located at the ORM, we present an analysis of the atmospheric dust content and its effects on astronomical observations. B, V and I dust aerosol astronomical extinction are derived. Using a 5 years series database of data taken from the four channel TNG dust monitor, we compute a mean hourly and daily values of the dust content. We have detected particles having size 0.3, 0.5, 1.0 and 5.0 um. Using a power law we have derived the content of 10.0 um particles. We found a typical local dust concentration ranging from 3x10^6 particles per cubic meter at 0.3 um, to 10^3 at 5.0 um and 10 at 10.0 um, increasing up to 3 order of magnitudes during the dust storms, with a relative higher increase o...

  12. Profiling the atmospheric water vapor content using a GPS-Meteorology network

    E-Print Network [OSTI]

    Mountziaris, T. J.

    Profiling the atmospheric water vapor content using a GPS-Meteorology network Jayson Maldonado-Meteorological stations. Research Objectives · Develop the hardware necessary for the collection atmospheric water content gives the real Water Vapor Content (WVC) in 3D instead of the Zenith Delay. Future Work · Testing

  13. X-RAY ABSORPTION SPECTROSCOPY FOR THE CHEMICAL CHARACTERIZATION OF ATMOSPHERIC AEROSOLS

    E-Print Network [OSTI]

    Jaklevic, J. M.

    2011-01-01

    aerosol samples and on fly ash samples obtained from powerMajor elements present in fly ash samples obtained both in-

  14. Atmospheric Measurements of Submicron Aerosols at the California-Mexico Border and in Houston, Texas 

    E-Print Network [OSTI]

    Levy, Misti E

    2013-04-29

    as the concentration of Mexico, the submicron aerosols are heavily influenced by vehicle emissions. We observe an average single scattering albedo of 0...

  15. Environmental Chamber Study of Atmospheric Chemistry and Secondary Organic Aerosol Formation Using Cavity Enhanced Absorption Spectroscopy

    E-Print Network [OSTI]

    Liu, Yingdi

    2011-01-01

    modelling: a review. Atmospheric Chemistry and Physics,emerging issues. Atmospheric Chemistry and Physics, 2009. 9:aqueous phase. Atmospheric Chemistry and Physics, 2009. 9:

  16. Chemistry of atmospheric aerosol particles and their resulting warm cloud-nucleation properties

    E-Print Network [OSTI]

    Moore, Meagan Julia Kerry

    2011-01-01

    for CCN activation, Atmospheric Chemistry and Physics, 10,and precipitation, Atmospheric Chemistry and Physics, 9,dust particles. Atmospheric Chemistry and Physics, 2009, 9,

  17. Chemistry of atmospheric aerosol particles and their resulting warm cloud-nucleation properties

    E-Print Network [OSTI]

    Moore, Meagan Julia Kerry

    2011-01-01

    CCN activation, Atmospheric Chemistry and Physics, 10, 5241-precipitation, Atmospheric Chemistry and Physics, 9, 3223-particles. Atmospheric Chemistry and Physics, 2009, 9, A. P.

  18. Source identification of lead pollution in the atmosphere of Shanghai City by analyzing single aerosol particles (SAP)

    SciTech Connect (OSTI)

    Wang, J.; Guo, P.; Li, X. [and others] [and others

    2000-05-15

    A new method combining the pattern recognition (PR) technique with micro-PIXE spectrum was used for direct assessment of lead pollution in the atmosphere of Shanghai City. Single aerosol particles (SAP) of PM{sub 10} (<10 {micro}m) were analyzed using the nuclear microprobe. Every particle is characterized with its micro-PICE spectrum, which can be considered its fingerprint. The PR technique was applied to trace a lead contaminated aerosol particle back to its source. The discrimination of different pollutant sources was enhanced with investigating the individual aerosol particles. The results showed that the lead contamination from automobile exhaust should not be neglected. The lead concentration with low level was detected in most unleaded gasoline particles; however, the highest lead level of 1,500 ppm was found in one of them. Furthermore, four other main pollutant sources contributing to the lead contamination in the Shanghai atmosphere were clearly identified by this method. They are the cement industry, the coal combustion, the oil combustion, and the metallurgic industry. Some other unidentified particles suggested that some more lead emitters might also exist in Shanghai.

  19. Extending the physicochemical characterization of aerosol particles in California

    E-Print Network [OSTI]

    Zauscher, Melanie Dorothy

    2012-01-01

    Combustion Aerosol, Atmospheric Chemistry and Physics, 11 (Based Receptor Modeling, Atmospheric Chemistry and Physics,Aerosols, Journal of Atmospheric Chemistry, 22 (1-2), 19-39.

  20. Modeling the Direct and Indirect Effects of Atmospheric Aerosols on Tropical Cyclones 

    E-Print Network [OSTI]

    Lee, Keun-Hee

    2012-02-14

    The direct and indirect effects of aerosols on the hurricane ‘Katrina’ have been investigated using the WRF model with a two-moment bulk microphysical scheme and modified Goddard shortwave radiation scheme. Simulations of the hurricane ‘Katrina...

  1. Atmospheric Aerosols Aging Involving Organic Compounds and Impacts on Particle Properties 

    E-Print Network [OSTI]

    Qiu, Chong

    2013-02-01

    In the first part of this dissertation, we study the aging of soot, a representative type of primary aerosols, in the presence of OH-initiated oxidation products of toluene. Monodisperse soot particles are introduced into an environmental chamber...

  2. Real time in situ detection of organic nitrates in atmospheric aerosols

    E-Print Network [OSTI]

    Rollins, Andrew W.

    2011-01-01

    and Field Calibration. Aero. Sci. Tech. 1994, 21, 325 –Collected in Houston, Texas. Aero. Sci. Tech. 2002, 36,aerosol GC/MS- FID (TAG). Aero. Sci. Tech. 2006, 40, 627–

  3. Heterogeneous Surface-Based Freezing of Atmospheric Aerosols Containing Ash, Soot, and Soil 

    E-Print Network [OSTI]

    Fornea, Adam P.

    2010-07-14

    nucleation will occur through one of several mechanisms including the contact and immersion freezing mechanisms. Through a series of contact freezing experiments, we have characterized the ability of aerosols composed of volcanic ash, soot, and peat soil...

  4. Aerosol Effects on Cirrus through Ice Nucleation in the Community Atmosphere Model CAM5 with a Statistical Cirrus Scheme

    SciTech Connect (OSTI)

    Wang, Minghuai; Liu, Xiaohong; Zhang, Kai; Comstock, Jennifer M.

    2014-09-01

    A statistical cirrus cloud scheme that tracks ice saturation ratio in the clear-sky and cloudy portion of a grid box separately has been implemented into NCAR CAM5 to provide a consistent treatment of ice nucleation and cloud formation. Simulated ice supersaturation and ice crystal number concentrations strongly depend on the number concentrations of heterogeneous ice nuclei (IN), subgrid temperature formulas and the number concentration of sulfate particles participating in homogeneous freezing, while simulated ice water content is insensitive to these perturbations. 1% to 10% dust particles serving as heterogeneous IN is 20 found to produce ice supersaturaiton in better agreement with observations. Introducing a subgrid temperature perturbation based on long-term aircraft observations of meso-scale motion produces a better hemispheric contrast in ice supersaturation compared to observations. Heterogeneous IN from dust particles significantly alter the net radiative fluxes at the top of atmosphere (TOA) (-0.24 to -1.59 W m-2) with a significant clear-sky longwave component (0.01 to -0.55 W m-2). Different cirrus treatments significantly perturb the net TOA anthropogenic aerosol forcing from -1.21 W m-2 to -1.54 W m-2, with a standard deviation of 0.10 W m-2. Aerosol effects on cirrus clouds exert an even larger impact on the atmospheric component of the radiative fluxes (two or three times the changes in the TOA radiative fluxes) and therefore on the hydrology cycle through the fast atmosphere response. This points to the urgent need to quantify aerosol effects on cirrus clouds through ice nucleation and how these further affect the hydrological cycle.

  5. El Roque de Los Muchachos Site Characteristics. III. Analysis of Atmospheric Dust and Aerosol Extinction

    E-Print Network [OSTI]

    G. Lombardi; V. Zitelli; S. Ortolani; M. Pedani; A. Ghedina

    2008-03-26

    Canary Islands are normally interested by dominant North-East winds that, in some meteorological conditions, can transport sand at high altitude from the Sahara desert. The dust may affect the efficiency of the telescopes and decreases the transparency of the sky. In order to maximize the scientific return of the telescopes located at the ORM, we present an analysis of the atmospheric dust content and its effects on astronomical observations. B, V and I dust aerosol astronomical extinction are derived. Using a 5 years series database of data taken from the four channel TNG dust monitor, we compute a mean hourly and daily values of the dust content. We have detected particles having size 0.3, 0.5, 1.0 and 5.0 um. Using a power law we have derived the content of 10.0 um particles. We found a typical local dust concentration ranging from 3x10^6 particles per cubic meter at 0.3 um, to 10^3 at 5.0 um and 10 at 10.0 um, increasing up to 3 order of magnitudes during the dust storms, with a relative higher increase of 1.0, 5.0 and 10.0 um particles. The number of local dust storm events is the same in winter- and summertime, but, the average background and storm-related increases in the dust concentration in summer are significantly higher than in winter. In a uniform approximation, during the dust storms, an average height of the dust layer of 2.5 km above the telescope is inferred. During the sand storms La Palma Island is affected by an almost uniform layer extending up to 5 km above the sea level, down, at least the height of the telescope. The visible extinction is dominated by particles at 1.0, 5.0 and 10.0 um. In agreement with the results from Carlsberg Automatic Meridian Circle (CAMC) we find a typical extinction during dust storms of about 0.2 mag/airmass.

  6. ERRORS IN VIKING LANDER ATMOSPHERIC PROFILES DISCOVERED USING MOLA TOPOGRAPHY. Paul Withers1

    E-Print Network [OSTI]

    Withers, Paul

    ERRORS IN VIKING LANDER ATMOSPHERIC PROFILES DISCOVERED USING MOLA TOPOGRAPHY. Paul Withers1 , R. D above the spatially-varying martian topography, were used to constrain the reconstructed trajectory of martian topography pro- vided by the laser altimeter (MOLA) aboard the Mars Global Surveyor spacecraft

  7. Evaluating Global Aerosol Models and Aerosol and Water Vapor Properties Near Clouds

    SciTech Connect (OSTI)

    Turner, David, D.; Ferrare, Richard, A.

    2011-07-06

    The 'Evaluating Global Aerosol Models and Aerosol and Water Vapor Properties Near Clouds' project focused extensively on the analysis and utilization of water vapor and aerosol profiles derived from the ARM Raman lidar at the Southern Great Plains ARM site. A wide range of different tasks were performed during this project, all of which improved quality of the data products derived from the lidar or advanced the understanding of atmospheric processes over the site. These activities included: upgrading the Raman lidar to improve its sensitivity; participating in field experiments to validate the lidar aerosol and water vapor retrievals; using the lidar aerosol profiles to evaluate the accuracy of the vertical distribution of aerosols in global aerosol model simulations; examining the correlation between relative humidity and aerosol extinction, and how these change, due to horizontal distance away from cumulus clouds; inferring boundary layer turbulence structure in convective boundary layers from the high-time-resolution lidar water vapor measurements; retrieving cumulus entrainment rates in boundary layer cumulus clouds; and participating in a field experiment that provided data to help validate both the entrainment rate retrievals and the turbulent profiles derived from lidar observations.

  8. Atmospheric Aerosol Monitoring from Satellite Observations: A History of Three Decades

    E-Print Network [OSTI]

    Zeng, Ning

    and energy and water cycles, and the involvement of aerosols with the dynamic system. The synergetic use of data from different satellite sensors provides more comprehen- sive information to better quantify (e.g., pollens, sea- salt, wind-blown dust, volcanic ash) or from man- made sources (e.g., smoke

  9. 1. Introduction The aerosol DRE at the top-of-atmosphere

    E-Print Network [OSTI]

    Graaf, Martin de

    is the incident solar irradiance spectrum. The anisotropy factor , a measure for the angular distribution observed aerosol DRE in a case of smoke over clouds off the west coast of Africa was 69±7 Wm-2 (ESA) within the Support to Science Element, project number 22403. µ0E0 Figure 2. CALIOP 1064 nm

  10. ATMOSPHERIC AND OCEANIC SCIENCE LETTERS, 2013, VOL. 6, NO. 1, 39-43 Effects of Clouds and Aerosols on Surface Radiation Budget Inferred from

    E-Print Network [OSTI]

    Dong, Xiquan

    of Atmospheric Physics, NUIST, Nanjing 210044, China 3 Global Change and Earth System Science (GCESS), Beijing Radiative Effects (AREs) are 12.7, ­37.6, and ­24.9 W m­2 , indicating that aerosols have LW warming impact have much stronger LW warming effect and SW cooling effect on the surface radiation budget than AREs

  11. Future Scientific Directions: Coupling between land ecosystems and the atmospheric hydrologic cycle through biogenic aerosol pathways

    E-Print Network [OSTI]

    Nenes, Athanasios

    , College Station, TX Robert Griffin University of New Hampshire, Durham, NH Michael Hannigan University Athanasios Nenes Georgia Institute of Technology, Atlanta, GA Mark Potosnak National Center for Atmospheric

  12. Research by BNL investigators was performed under the auspices of the U.S. Department of Energy under Contract No. DE-AC02-DOE research on atmospheric aerosols

    E-Print Network [OSTI]

    Division, the Atmospheric Radiation Measurement (ARM) Program and the Atmospheric Chemistry Program (ACP of Energy under Contract No. DE-AC02- 98CH10886. BNL-62609 DOE research on atmospheric aerosols S are an programs dealing with atmospheric science, subsurface science, environmental radon, ocean margins

  13. Initial Assessment of the Spectrometer for Sky-Scanning, Sun-Tracking Atmospheric Research (4STAR)-Based Aerosol Retrieval: Sensitivity Study

    SciTech Connect (OSTI)

    Kassianov, Evgueni I.; Flynn, Connor J.; Redemann, Jens; Schmid, Beat; Russell, P. B.; Sinyuk, Alexander

    2012-10-24

    The Spectrometer for Sky-Scanning, Sun-Tracking Atmospheric Research (4STAR) being developed for airborne measurements will offer retrievals of aerosol microphysical and optical properties from multi-angular and multi-spectral measurements of sky radiance and direct-beam sun transmittance. In this study, we assess the expected accuracy of the 4STAR-based aerosol retrieval and its sensitivity to major sources of anticipated perturbations in the 4STAR measurements by adapting a theoretical approach previously developed for the AERONET measurements. The major anticipated perturbations are (1) an apparent enhancement of sky radiance at small scattering angles associated with the necessarily compact design of the 4STAR and (2) and an offset (i.e. uncertainty) of sky radiance calibration independent of scattering angle. The assessment is performed through application of the operational AERONET aerosol retrieval and constructed synthetic 4STAR-like data. Particular attention is given to the impact of these perturbations on the upwelling and downwelling broadband fluxes and the direct aerosol radiative forcing at the bottom and top of the atmosphere. The results from this study suggest that limitations in the accuracy of 4STAR-retrieved particle size distributions and scattering phase functions have diminished impact on the accuracy of retrieved bulk microphysical parameters, permitting quite accurate retrievals of properties including the effective radius (up to 10%, or 0.03), and the radiatively important optical properties, such as the asymmetry factor (up to 4%, or ±0.02) and single-scattering albedo (up to 6%, or ±0.04). Also, the obtained results indicate that the uncertainties in the retrieved aerosol optical properties are quite small in the context of the calculated fluxes and direct aerosol radiative forcing (up to 15%, or 3 Wm-2).

  14. Development and Characterization of a Thermodenuder for Aerosol Volatility Measurements

    SciTech Connect (OSTI)

    Dr. Timothy Onasch

    2009-09-09

    This SBIR Phase I project addressed the critical need for improved characterization of carbonaceous aerosol species in the atmosphere. The proposed work focused on the development of a thermodenuder (TD) system capable of systematically measuring volatility profiles of primary and secondary organic aerosol species and providing insight into the effects of absorbing and nonabsorbing organic coatings on particle absorption properties. This work provided the fundamental framework for the generation of essential information needed for improved predictions of ambient aerosol loadings and radiative properties by atmospheric chemistry models. As part of this work, Aerodyne Research, Inc. (ARI) continued to develop and test, with the final objective of commercialization, an improved thermodenuder system that can be used in series with any aerosol instrument or suite of instruments (e.g., aerosol mass spectrometers-AMS, scanning mobility particle sizers-SMPS, photoacoustic absorption spectrometers-PAS, etc.) to obtain aerosol chemical, physical, and optical properties as a function of particle volatility. In particular, we provided the proof of concept for the direct coupling of our improved TD design with a full microphysical model to obtain volatility profiles for different organic aerosol components and to allow for meaningful comparisons between different TD-derived aerosol measurements. In a TD, particles are passed through a heated zone and a denuding (activated charcoal) zone to remove semi-volatile material. Changes in particle size, number concentration, optical absorption, and chemical composition are subsequently detected with aerosol instrumentation. The aerosol volatility profiles provided by the TD will strengthen organic aerosol emission inventories, provide further insight into secondary aerosol formation mechanisms, and provide an important measure of particle absorption (including brown carbon contributions and identification, and absorption enhancements due to coatings on soot particles). The successfully completed Phase I project included construction of a prototype design for the TD with detailed physical modeling, testing with laboratory and ambient aerosol particles, and the initiation of a detailed microphysical model of the aerosol particles passing through the TD to extract vapor pressure distributions. The objective of the microphysical model is to derive vapor pressure distributions (i.e. vapor pressure ranges, including single chemical compounds, mixtures of known compounds, and complex ‘real-world’ aerosols, such as SOA, and soot particles with absorbing and nonabsorbing coatings) from TD measurements of changes in particle size, mass, and chemical composition for known TD temperatures and flow rates (i.e. residence times). The proposed Phase II project was designed to optimize several TD systems for different instrument applications and to combine the hardware and modeling into a robust package for commercial sales.

  15. ATMOSPHERIC AEROSOL SOURCE-RECEPTOR RELATIONSHIPS: THE ROLE OF COAL-FIRED POWER PLANTS

    SciTech Connect (OSTI)

    Allen L. Robinson; Spyros N. Pandis; Cliff I. Davidson

    2005-04-01

    This report describes the technical progress made on the Pittsburgh Air Quality Study (PAQS) during the period of September 2004 through February 2005. Significant progress was made this project period on the analysis of ambient data, source apportionment, and deterministic modeling activities. The major experimental achievement this project period was the characterization of the mercury and fine particle emissions from two modern, large, commercial pulverized coal boilers. This testing completes the field work component of the Source Characterization Activity. This report highlights results from mercury emission measurements made using a dilution sampler. The measurements clearly indicate that mercury is being transformed from an oxidized to an elemental state within the dilution. However, wall effects are significant making it difficult to determine whether or not these changes occur in the gas phase or due to some interaction with the sampler walls. This report also presents results from an analysis that uses spherical aluminum silicate (SAS) particles as a marker for primary PM{sub 2.5} emitted from coal combustion. Primary emissions from coal combustion contribute only a small fraction of the PM{sub 2.5} mass (less than 1.5% in the summer and less than 3% in the winter) at the Pittsburgh site. Ambient SAS concentrations also appear to be reasonably spatially homogeneous. Finally, SAS emission factors measured at pilot-scale are consistent with measurements made at full-scale. This report also presents results from applying the Unmix and PMF models to estimate the contribution of different sources to the PM{sub 2.5} mass concentrations in Pittsburgh using aerosol composition information. Comparison of the two models shows similar source composition and contribution for five factors: crustal material, nitrate, an Fe, Mn, and Zn factor, specialty steel production, and a cadmium factor. PMF found several additional factors. Comparison between source contributions for the similar factors shows reasonable agreement between the two models. The sulfate factor shows the highest contribution to local PM{sub 2.5} with an annual average contribution of approximately 28% (from PMF). The nitrate, crustal material, and primary OC and EC factors also show significant contributions on the order of 10-14%. The sulfate factor is affected by photochemistry and therefore shows maximum values in summer.

  16. A Sensitivity Study of Radiative Fluxes at the Top of Atmosphere to Cloud-Microphysics and Aerosol Parameters in the Community Atmosphere Model CAM5

    SciTech Connect (OSTI)

    Zhao, Chun; Liu, Xiaohong; Qian, Yun; Yoon, Jin-Ho; Hou, Zhangshuan; Lin, Guang; McFarlane, Sally A.; Wang, Hailong; Yang, Ben; Ma, Po-Lun; Yan, Huiping; Bao, Jie

    2013-11-08

    In this study, we investigated the sensitivity of net radiative fluxes (FNET) at the top of atmosphere (TOA) to 16 selected uncertain parameters mainly related to the cloud microphysics and aerosol schemes in the Community Atmosphere Model version 5 (CAM5). We adopted a quasi-Monte Carlo (QMC) sampling approach to effectively explore the high dimensional parameter space. The output response variables (e.g., FNET) were simulated using CAM5 for each parameter set, and then evaluated using generalized linear model analysis. In response to the perturbations of these 16 parameters, the CAM5-simulated global annual mean FNET ranges from -9.8 to 3.5 W m-2 compared to the CAM5-simulated FNET of 1.9 W m-2 with the default parameter values. Variance-based sensitivity analysis was conducted to show the relative contributions of individual parameter perturbation to the global FNET variance. The results indicate that the changes in the global mean FNET are dominated by those of cloud forcing (CF) within the parameter ranges being investigated. The size threshold parameter related to auto-conversion of cloud ice to snow is confirmed as one of the most influential parameters for FNET in the CAM5 simulation. The strong heterogeneous geographic distribution of FNET variation shows parameters have a clear localized effect over regions where they are acting. However, some parameters also have non-local impacts on FNET variance. Although external factors, such as perturbations of anthropogenic and natural emissions, largely affect FNET variations at the regional scale, their impact is weaker than that of model internal parameters in terms of simulating global mean FNET in this study. The interactions among the 16 selected parameters contribute a relatively small portion of the total FNET variations over most regions of the globe. This study helps us better understand the CAM5 model behavior associated with parameter uncertainties, which will aid the next step of reducing model uncertainty via calibration of uncertain model parameters with the largest sensitivity.

  17. The Indirect and Semi-Direct Aerosol Campaign

    SciTech Connect (OSTI)

    Ghan, Steve

    2014-03-24

    Research projects like the Indirect and Semi-Direct Aerosol Campaign, or ISDAC, increase our knowledge of atmospheric aerosol particles and cloud physics.

  18. ARM - Field Campaign - Aerosol and Cloud Experiments in the Eastern...

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    horizontal variabilities of aerosol, trace gases, cloud, drizzle, and atmospheric thermodynamics are critically needed for understanding and quantifying the budget of MBL aerosol,...

  19. The Indirect and Semi-Direct Aerosol Campaign

    ScienceCinema (OSTI)

    Ghan, Steve

    2014-06-12

    Research projects like the Indirect and Semi-Direct Aerosol Campaign, or ISDAC, increase our knowledge of atmospheric aerosol particles and cloud physics.

  20. Oxidation of atmospheric organic carbon : interconnecting volatile organic compounds, intermediate-volatility organic compounds, and organic aerosol

    E-Print Network [OSTI]

    Hunter, James Freeman

    2015-01-01

    .Organic molecules have many important roles in the atmosphere, acting as climate and biogeochemical forcers, and in some cases as toxic pollutants. The lifecycle of atmospheric organic carbon is extremely complex, with ...

  1. Aircraft vertical profiles of trace gas and aerosol pollution over the mid-Atlantic United States: Statistics and meteorological cluster

    E-Print Network [OSTI]

    Thompson, Anne

    measurements of O3, CO, SO2, and aerosol properties were made during summertime air pollution episodes over. Introduction [2] In 1992, in response to mounting air pollution prob- lems over the mid-Atlantic United States holistic, long-term air quality studies in the region and analyzing transboundary pollution transport

  2. The middle Martian atmosphere

    SciTech Connect (OSTI)

    Jaquin, R.F.

    1989-01-01

    Profiles of scattered light above the planetary limb from 116 Viking Orbiter images are used to constrain the temporal and spatial behavior of aerosols suspended in the Martian atmosphere. The data cover a wide range of seasons, locations, and viewing geometry, providing information about the aerosol optical properties and vertical distribution. The typical atmospheric column contains one or more discrete, optically thin, ice-like haze layers between 30 and 90 km elevation whose composition is inferred to be water ice. Below the detached hazes, a continuous haze, interpreted to have a large dust component, extends from as much as 50 km to the surface. The haze distribution exhibits an annual variation that reflects a seasonally driven circulation in the middle atmosphere. The potential role of stationary gravity waves in modifying the middle atmosphere circulation is explored using a linear theory applied to a realistic Martian environment. Martian topography derived from radar observations is decomposed into Fourier harmonics and used to linearly superpose gravity waves arising from each component. The larger amplitude topography on Mars combined with the absence of extended regions of smooth topography like oceans generates larger wave amplitudes than on the Earth. The circulation of the middle atmosphere is examined using a two-dimensional, linearized, axisymmetric model successfully employed in the study of the terrestrial mesosphere. Illustrations of temperature and wind speeds are presented for the southern summer solstice and southern spring equinox.

  3. Aerosol remote sensing in polar regions

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Tomasi, Claudio; Kokhanovsky, Alexander A.; Lupi, Angelo; Ritter, Christoph; Smirnov, Alexander; O'Neill, Norman T.; Stone, Robert S.; Holben, Brent N.; Nyeki, Stephan; Wehrli, Christoph; et al

    2015-01-01

    Multi-year sets of ground-based sun-photometer measurements conducted at 12 Arctic sites and 9 Antarctic sites were examined to determine daily mean values of aerosol optical thickness ?(?) at visible and near-infrared wavelengths, from which best-fit values of Ĺngström's exponent ? were calculated. Analysing these data, the monthly mean values of ?(0.50 ?m) and ? and the relative frequency histograms of the daily mean values of both parameters were determined for winter–spring and summer–autumn in the Arctic and for austral summer in Antarctica. The Arctic and Antarctic covariance plots of the seasonal median values of ? versus ?(0.50 ?m) showed: (i)more »a considerable increase in ?(0.50 ?m) for the Arctic aerosol from summer to winter–spring, without marked changes in ?; and (ii) a marked increase in ?(0.50 ?m) passing from the Antarctic Plateau to coastal sites, whereas ? decreased considerably due to the larger fraction of sea-salt aerosol. Good agreement was found when comparing ground-based sun-photometer measurements of ?(?) and ? at Arctic and Antarctic coastal sites with Microtops measurements conducted during numerous AERONET/MAN cruises from 2006 to 2013 in three Arctic Ocean sectors and in coastal and off-shore regions of the Southern Atlantic, Pacific, and Indian Oceans, and the Antarctic Peninsula. Lidar measurements were also examined to characterise vertical profiles of the aerosol backscattering coefficient measured throughout the year at Ny-Ĺlesund. Satellite-based MODIS, MISR, and AATSR retrievals of ?(?) over large parts of the oceanic polar regions during spring and summer were in close agreement with ship-borne and coastal ground-based sun-photometer measurements. An overview of the chemical composition of mode particles is also presented, based on in-situ measurements at Arctic and Antarctic sites. Fourteen log-normal aerosol number size-distributions were defined to represent the average features of nuclei, accumulation and coarse mode particles for Arctic haze, summer background aerosol, Asian dust and boreal forest fire smoke, and for various background austral summer aerosol types at coastal and high-altitude Antarctic sites. The main columnar aerosol optical characteristics were determined for all 14 particle modes, based on in-situ measurements of the scattering and absorption coefficients. Diurnally averaged direct aerosol-induced radiative forcing and efficiency were calculated for a set of multimodal aerosol extinction models, using various Bidirectional Reflectance Distribution Function models over vegetation-covered, oceanic and snow-covered surfaces. These gave a reliable measure of the pronounced effects of aerosols on the radiation balance of the surface–atmosphere system over polar regions.« less

  4. Aerosol remote sensing in polar regions

    SciTech Connect (OSTI)

    Tomasi, Claudio; Kokhanovsky, Alexander A.; Lupi, Angelo; Ritter, Christoph; Smirnov, Alexander; O'Neill, Norman T.; Stone, Robert S.; Holben, Brent N.; Nyeki, Stephan; Mazzola, Mauro; Lanconelli, Christian; Vitale, Vito; Stebel, Kerstin; Aaltonen, Veijo; de Leeuw, Gerrit; Rodriguez, Edith; Herber, Andreas B.; Radionov, Vladimir F.; Zielinski, Tymon; Petelski, Tomasz; Sakerin, Sergey M.; Kabanov, Dmitry M.; Xue, Yong; Mei, Linlu; Istomina, Larysa; Wagener, Richard; McArthur, Bruce; Sobolewski, Piotr S.; Kivi, Rigel; Courcoux, Yann; Larouche, Pierre; Broccardo, Stephen; Piketh, Stuart J.

    2015-01-01

    Multi-year sets of ground-based sun-photometer measurements conducted at 12 Arctic sites and 9 Antarctic sites were examined to determine daily mean values of aerosol optical thickness ?(?) at visible and near-infrared wavelengths, from which best-fit values of Ĺngström's exponent ? were calculated. Analysing these data, the monthly mean values of ?(0.50 ?m) and ? and the relative frequency histograms of the daily mean values of both parameters were determined for winter–spring and summer–autumn in the Arctic and for austral summer in Antarctica. The Arctic and Antarctic covariance plots of the seasonal median values of ? versus ?(0.50 ?m) showed: (i) a considerable increase in ?(0.50 ?m) for the Arctic aerosol from summer to winter–spring, without marked changes in ?; and (ii) a marked increase in ?(0.50 ?m) passing from the Antarctic Plateau to coastal sites, whereas ? decreased considerably due to the larger fraction of sea-salt aerosol. Good agreement was found when comparing ground-based sun-photometer measurements of ?(?) and ? at Arctic and Antarctic coastal sites with Microtops measurements conducted during numerous AERONET/MAN cruises from 2006 to 2013 in three Arctic Ocean sectors and in coastal and off-shore regions of the Southern Atlantic, Pacific, and Indian Oceans, and the Antarctic Peninsula. Lidar measurements were also examined to characterise vertical profiles of the aerosol backscattering coefficient measured throughout the year at Ny-Ĺlesund. Satellite-based MODIS, MISR, and AATSR retrievals of ?(?) over large parts of the oceanic polar regions during spring and summer were in close agreement with ship-borne and coastal ground-based sun-photometer measurements. An overview of the chemical composition of mode particles is also presented, based on in-situ measurements at Arctic and Antarctic sites. Fourteen log-normal aerosol number size-distributions were defined to represent the average features of nuclei, accumulation and coarse mode particles for Arctic haze, summer background aerosol, Asian dust and boreal forest fire smoke, and for various background austral summer aerosol types at coastal and high-altitude Antarctic sites. The main columnar aerosol optical characteristics were determined for all 14 particle modes, based on in-situ measurements of the scattering and absorption coefficients. Diurnally averaged direct aerosol-induced radiative forcing and efficiency were calculated for a set of multimodal aerosol extinction models, using various Bidirectional Reflectance Distribution Function models over vegetation-covered, oceanic and snow-covered surfaces. These gave a reliable measure of the pronounced effects of aerosols on the radiation balance of the surface–atmosphere system over polar regions.

  5. Chemical and Physical Properties of Atmospheric Aerosols (a) A Case Study in the Unique Properties of Agricultural Aerosols (b) The Role of Chemical Composition in Ice Nucleation during the Arctic Spring 

    E-Print Network [OSTI]

    Moon, Seong-Gi

    2011-08-08

    dataset is reported for these physical and chemical properties of agricultural aerosols appropriate for use in a site-specific emission inventory. The emission rate and transport of the aerosols are also discussed. In addition, mixing ratios of total...

  6. Mechanism of the hydroxy radical oxidation of methacryoyl peroxynitrate (MPAN) and its pathway toward secondary organic aerosol formation in the atmosphere

    SciTech Connect (OSTI)

    Nguyen, Tran B.; Bates, Kelvin H.; Crounse, J. D.; Schwantes, Rebecca H.; Zhang, Xuan; Kjaergaard, Henrik G.; Surratt, Jason D.; Lin, Peng; Laskin, Alexander; Seinfeld, John H.; Wennberg, P. O.

    2015-01-01

    Methacryoyl peroxynitrate (MPAN), the acylperoxyl nitrate of methacrolein, has been suggested to be an important secondary organic aerosol (SOA) precursor from isoprene oxidation. Yet, the mechanism by which MPAN produces SOA via reaction with the hydroxyl radical (OH) is unclear. We systematically evaluate three proposed mechanisms in controlled chamber experiments and provide the first experimental support for the theoretically-predicted lactone formation pathway from the MPAN + OH reaction, producing hydroxymethyl-methyl-?-lactone (HMML). The decomposition of the MPAN-OH adduct yields HMML + NO3 (~ 75%) and hydroxyacetone + CO + NO3 (~ 25%), out-competing its reaction with atmospheric oxygen. The production of other proposed SOA precursors, e.g., methacrylic acid epoxide (MAE), from MPAN and methacrolein are negligible (< 2 %). Furthermore, we show that the beta-alkenyl moiety of MPAN is critical for lactone formation. Alkyl radicals formed via OH abstraction nstead of addition are thermalized; thus, even if they are structurally identical to the MPAN-OH adduct, they do not decompose to HMML. The SOA formation from HMML, via polyaddition of the lactone to organic compounds, is close to unity under dry conditions. However, the SOA yield is sensitive to particle liquid water and solvated ions. In hydrated sulfate-containing particles, HMML reacts primarily with H2O and aqueous sulfate, producing monomeric 2-methylglyceric acid (2MGA) and the associated organosulfate. 2MGA, a tracer for isoprene SOA, is semivolatile and its volatility increases with decreasing pH in the aerosol water. Conditions that enhance the production of neutral 2MGA will suppress SOA mass from the HMML channel. Considering the liquid water content and pH ranges of ambient particles, MGA may exist largely as a gaseous compound in some parts of the atmosphere.

  7. Source profiles for nonmethane organic compounds in the atmosphere of Cairo, Egypt.

    SciTech Connect (OSTI)

    Doskey, P. V.; Fukui, Y.; Sultan, M.; Maghraby, A. A.; Taher, A.; Environmental Research; Cairo Univ.

    1999-07-01

    Profiles of the sources of nonmethane organic compounds (NMOCs) were developed for emissions from vehicles, petroleum fuels (gasoline, liquefied petroleum gas (LPG), and natural gas), a petroleum refinery, a smelter, and a cast iron factory in Cairo, Egypt. More than 100 hydrocarbons and oxygenated hydrocarbons were tentatively identified and quantified. Gasoline-vapor and whole-gasoline profiles could be distinguished from the other profiles by high concentrations of the C{sub 5} and C{sub 6} saturated hydrocarbons. The vehicle emission profile was similar to the whole-gasoline profile, with the exception of the unsaturated and aromatic hydrocarbons, which were present at higher concentrations in the vehicle emission profile. High levels of the C{sub 2}-C{sub 4} saturated hydrocarbons, particularly n-butane, were characteristic features of the petroleum refinery emissions. The smelter and cast iron factory emissions were similar to the refinery emissions; however, the levels of benzene and toluene were greater in the former two sources. The LPG and natural gas emissions contained high concentrations of n-butane and ethane, respectively. The NMOC source profiles for Cairo were distinctly different from profiles for U.S. sources, indicating that NMOC source profiles are sensitive to the particular composition of petroleum fuels that are used in a location.

  8. A new aerosol collector for quasi on-line analysis of particulate organic matter: the Aerosol Collection Module (ACM) and first applications with a GC/MS-FID

    E-Print Network [OSTI]

    Hohaus, T.

    In many environments organic matter significantly contributes to the composition of atmospheric aerosol particles influencing its properties. Detailed chemical characterization of ambient aerosols is critical in order to ...

  9. Direct Aerosol Forcing Uncertainty

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Mccomiskey, Allison

    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.

  10. Direct Aerosol Forcing Uncertainty

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    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.

  11. Aerosol properties, in-canopy gradients, turbulent fluxes and VOC concentrations at a pristine forest site in Amazonia

    E-Print Network [OSTI]

    Rizzo, LV; Artaxo, P; Karl, T; Guenther, AB; Greenberg, J

    2010-01-01

    wet season. Atmospheric Chemistry and Physics Discussions 9,carbonaceous aerosols. Atmospheric Chemistry and Physics 6,of the EU project OSOA. Atmospheric Chemistry and Physics 4,

  12. Correlations in the chemical composition of rural background atmospheric aerosol in the UK determined in real time using time-of-flight mass spectrometry 

    E-Print Network [OSTI]

    Beddows, David C S; Donovan, Robert J; Harrison, Roy M; Heal, Mathew R; Kinnersley, Robert P; King, Martin; Nicholson, David; Thompson, Katherine

    2004-01-01

    polluted air mass that had passed over the British mainland before reaching Eskdalemuir, interposed between two cleaner air masses that had arrived directly from the sea. Such changes in the background aerosol could clearly be very important to studies...

  13. Hyperspectral Aerosol Optical Depths from TCAP Flights

    SciTech Connect (OSTI)

    Shinozuka, Yohei; Johnson, Roy R.; Flynn, Connor J.; Russell, P. B.; Schmid, Beat; Redemann, Jens; Dunagan, Stephen; Kluzek, Celine D.; Hubbe, John M.; Segal-Rosenheimer, Michal; Livingston, J. M.; Eck, T.; Wagener, Richard; Gregory, L.; Chand, Duli; Berg, Larry K.; Rogers, Ray; Ferrare, R. A.; Hair, John; Hostetler, Chris A.; Burton, S. P.

    2013-11-13

    4STAR (Spectrometer for Sky-Scanning, Sun-Tracking Atmospheric Research), the world’s first hyperspectral airborne tracking sunphotometer, acquired aerosol optical depths (AOD) at 1 Hz during all July 2012 flights of the Two Column Aerosol Project (TCAP). Root-mean square differences from AERONET ground-based observations were 0.01 at wavelengths between 500-1020 nm, 0.02 at 380 and 1640 nm and 0.03 at 440 nm in four clear-sky fly-over events, and similar in ground side-by-side comparisons. Changes in the above-aircraft AOD across 3-km-deep spirals were typically consistent with integrals of coincident in situ (on DOE Gulfstream 1 with 4STAR) and lidar (on NASA B200) extinction measurements within 0.01, 0.03, 0.01, 0.02, 0.02, 0.02 at 355, 450, 532, 550, 700, 1064 nm, respectively, despite atmospheric variations and combined measurement uncertainties. Finer vertical differentials of the 4STAR measurements matched the in situ ambient extinction profile within 14% for one homogeneous column. For the AOD observed between 350-1660 nm, excluding strong water vapor and oxygen absorption bands, estimated uncertainties were ~0.01 and dominated by (then) unpredictable throughput changes, up to +/-0.8%, of the fiber optic rotary joint. The favorable intercomparisons herald 4STAR’s spatially-resolved high-frequency hyperspectral products as a reliable tool for climate studies and satellite validation.

  14. Experimental Characterization Of The Asymmetry And The Dip Form Of The H{sub {beta}}-Line Profiles In Microwave-Produced Plasmas At Atmospheric Pressure

    SciTech Connect (OSTI)

    Palomares, J. M.; Torres, J.; Gamero, A.; Sola, A. [Departamento de Fisica, Universidad de Cordoba. Campus Universitario de Rabanales C2. E-14071 Cordoba (Spain); Gigosos, M. A. [Departamento de Optica, Universidad de Valladolid. Campus Universitario de la Merced. E-47072 Valladolid Spain (Spain); Mullen, J. J. A. M. van der [Department of Applied Physics, Eindhoven University of Technology. P.O. Box 513. 5600 MD Eindhoven (Netherlands)

    2008-10-22

    An experimental study on the asymmetry of the Balmer H{sub {beta}} profile in plasmas produced by microwaves at atmospheric pressure is presented. The asymmetry of the whole profile is studied with the help of one function that quantified this characteristic. The asymmetry and shape of the central valley is also studied with the definition of several parameters. The study shows the presence of the Stark asymmetry in plasmas with electron density of the order of 10{sup 21}m{sup -3}.

  15. Marine aerosols

    E-Print Network [OSTI]

    Saltzman, ES

    2009-01-01

    proper- ties found in the marine boundary layer over theand R. E. Larson (1994), Marine boundary layer measurementsand T. Hoffmann (2002), Marine aerosol formation from

  16. Climatic effects of different aerosol types in China simulated

    E-Print Network [OSTI]

    Y. GU

    2006-01-01

    P. Shettle (1991), Atmospheric Aero- sols—Global ClimatologyEffects of stratospheric aero- sols and preliminarytypes, such as volcanic aero- sols, desert aerosols, or

  17. Reduction of photosynthetically active radiation under extreme stratospheric aerosol loads

    SciTech Connect (OSTI)

    Gerstl, S.A.W.; Zardecki, A.

    1981-08-01

    The recently published hypothesis that the Cretaceous-Tertiary extinctions might be caused by an obstruction of sunlight is tested by model calculations. First we compute the total mass of stratospheric aerosols under normal atmospheric conditions for four different (measured) aerosol size distributions and vertical profiles. For comparison, the stratospheric dust masses after four volcanic eruptions are also evaluated. Detailed solar radiative transfer calculations are then performed for artificially increased aerosol amounts until the postulated darkness scenario is obtained. Thus we find that a total stratospheric aerosol mass between 1 and 4 times 10/sup 1/ g is sufficient to reduce photosynthesis to 10/sup -3/ of normal. We also infer from this result tha the impact of a 0.4- to 3-km-diameter asteroid or a close encounter with a Halley-size comet may deposit that amount of particulates into the stratosphere. The darkness scenario of Alvarez et al. is thus shown to be a possible extinction mechanism, even with smaller size asteroids of comets than previously estimated.

  18. Gas-phase chemistry dominates O3 loss to a forest, implying a source of aerosols and hydroxyl radicals to the atmosphere

    E-Print Network [OSTI]

    Goldstein, Allen

    Gas-phase chemistry dominates O3 loss to a forest, implying a source of aerosols and hydroxyl into its major loss pathways; stomatal uptake, non-stomatal surface deposition, and gas-phase chemistry. Total O3 flux was dominated by gas-phase chemistry during the summer and by stomatal uptake during

  19. Final Report for �¢����Cloud-Aerosol Physics in Super-Parameterized Atmospheric Regional Climate Simulations (CAP-SPARCS)�¢��� (DE-SC0002003) for 8/15/2009 through 8/14/2012

    SciTech Connect (OSTI)

    Lynn M. Russell; Richard C.J. Somerville

    2012-11-05

    Improving the representation of local and non-local aerosol interactions in state-of-the-science regional climate models is a priority for the coming decade (Zhang, 2008). With this aim in mind, we have combined two new technologies that have a useful synergy: (1) an aerosol-enabled regional climate model (Advanced Weather Research and Forecasting Model with Chemistry WRF-Chem), whose primary weakness is a lack of high quality boundary conditions and (2) an aerosol-enabled multiscale modeling framework (PNNL Multiscale Aerosol Climate Model (MACM)), which is global but captures aerosol-convection-cloud feedbacks, and thus an ideal source of boundary conditions. Combining these two approaches has resulted in an aerosol-enabled modeling framework that not only resolves high resolution details in a particular region, but crucially does so within a global context that is similarly faithful to multi-scale aerosol-climate interactions. We have applied and improved the representation of aerosol interactions by evaluating model performance over multiple domains, with (1) an extensive evaluation of mid-continent precipitation representation by multiscale modeling, (2) two focused comparisons to transport of aerosol plumes to the eastern United States for comparison with observations made as part of the International Consortium for Atmospheric Research on Transport and Transformation (ICARTT), with the first being idealized and the second being linked to an extensive wildfire plume, and (3) the extension of these ideas to the development of a new approach to evaluating aerosol indirect effects with limited-duration model runs by �¢����nudging�¢��� to observations. This research supported the work of one postdoc (Zhan Zhao) for two years and contributed to the training and research of two graduate students. Four peer-reviewed publications have resulted from this work, and ground work for a follow-on project was completed.

  20. Group Report: Connections between Aerosol Properties

    E-Print Network [OSTI]

    effect and causes surface warming. Absorption of solar or thermal radiation within the atmospheric column-influencing constituents (such as green- house gases) by this process, anthropogenic aerosols can contribute to climate

  1. Characterizing Aerosol Distributions and Optical Properties Using the NASA Langley High Spectral Resolution Lidar

    SciTech Connect (OSTI)

    Hostetler, Chris; Ferrare, Richard

    2013-02-14

    The objective of this project was to provide vertically and horizontally resolved data on aerosol optical properties to assess and ultimately improve how models represent these aerosol properties and their impacts on atmospheric radiation. The approach was to deploy the NASA Langley Airborne High Spectral Resolution Lidar (HSRL) and other synergistic remote sensors on DOE Atmospheric Science Research (ASR) sponsored airborne field campaigns and synergistic field campaigns sponsored by other agencies to remotely measure aerosol backscattering, extinction, and optical thickness profiles. Synergistic sensors included a nadir-viewing digital camera for context imagery, and, later in the project, the NASA Goddard Institute for Space Studies (GISS) Research Scanning Polarimeter (RSP). The information from the remote sensing instruments was used to map the horizontal and vertical distribution of aerosol properties and type. The retrieved lidar parameters include profiles of aerosol extinction, backscatter, depolarization, and optical depth. Products produced in subsequent analyses included aerosol mixed layer height, aerosol type, and the partition of aerosol optical depth by type. The lidar products provided vertical context for in situ and remote sensing measurements from other airborne and ground-based platforms employed in the field campaigns and was used to assess the predictions of transport models. Also, the measurements provide a data base for future evaluation of techniques to combine active (lidar) and passive (polarimeter) measurements in advanced retrieval schemes to remotely characterize aerosol microphysical properties. The project was initiated as a 3-year project starting 1 January 2005. It was later awarded continuation funding for another 3 years (i.e., through 31 December 2010) followed by a 1-year no-cost extension (through 31 December 2011). This project supported logistical and flight costs of the NASA sensors on a dedicated aircraft, the subsequent analysis and archival of the data, and the presentation of results in conferences, workshops, and publications. DOE ASR field campaigns supported under this project included - MAX-Mex /MILAGRO (2006) - TexAQS 2006/GoMACCS (2006) - CHAPS (2007) - RACORO (2009) - CARE/CalNex (2010) In addition, data acquired on HSRL airborne field campaigns sponsored by other agencies were used extensively to fulfill the science objectives of this project and the data acquired have been made available to other DOE ASR investigators upon request.

  2. A geostatistical data fusion technique for merging remote sensing and groundbased observations of aerosol optical thickness

    E-Print Network [OSTI]

    Michalak, Anna M.

    that aerosols contrib- ute significantly to reflected solar radiation (the aerosol direct effect) and modify of aerosols in climate and atmospheric chemistry. To date, however, there have been only limited attempts of the growing concentrations of CO2 and other greenhouse gases. Although the radiative forcing of aerosols

  3. Simulated aerosol key optical properties over global scale using an aerosol transport model coupled with a new type of dynamic core

    E-Print Network [OSTI]

    Dong, Xiquan

    effects: (a) a direct effect in which aerosol particles scatter and absorb the solar and thermal radiation Atmospheric aerosols greatly impact the Earth's climate in many ways, and to date, not all of them are well

  4. Aerosol Science and Technology, 48:803812, 2014 Copyright C American Association for Aerosol Research

    E-Print Network [OSTI]

    Aerosol Science and Technology, 48:803­812, 2014 Copyright C American Association for Aerosol of particle growth in the atmosphere, and many properties of the resulting mixed particles depend on organic. In this article, analytic equations are derived p(;d) for condensational growth in a continuously mixed flow

  5. Evaluating Global Aerosol Models and Aerosol and Water Vapor Properties Near Clouds

    SciTech Connect (OSTI)

    Richard A. Ferrare; David D. Turner

    2011-09-01

    Project goals: (1) Use the routine surface and airborne measurements at the ARM SGP site, and the routine surface measurements at the NSA site, to continue our evaluations of model aerosol simulations; (2) Determine the degree to which the Raman lidar measurements of water vapor and aerosol scattering and extinction can be used to remotely characterize the aerosol humidification factor; (3) Use the high temporal resolution CARL data to examine how aerosol properties vary near clouds; and (4) Use the high temporal resolution CARL and Atmospheric Emitted Radiance Interferometer (AERI) data to quantify entrainment in optically thin continental cumulus clouds.

  6. Inferring middle atmospheric ozone height profiles from ground-based measurements of molecular oxygen emission rates. 2. Comparison with O[sub 2]([sup 1][Delta][sub g])(0,1) band measurements at sunset

    SciTech Connect (OSTI)

    Sica, R.J.; Lowe, R.P. (Univ. of Western Ontario, London (Canada))

    1993-01-20

    The ability to routinely acquire measurements of the ozone density profile in the mesosphere and lower thermosphere is important for use in chemical-dynamical models of the middle atmosphere. Zenith measurements of the O[sub 2]([sup 1][Delta][sub g]) (0,1) band emission rate in the evening twilight were acquired near the spring equinox of 1982 with a Michelson interferometer from London, Ontario, Canada. Knowledge of the change of the O[sub 2]([sup 1][Delta][sub g])(0,1) band emission rate at twilight can be related directly to ozone density, since ozone destruction by sunlight is the primary source of O[sub 2]([sup 1][Delta][sub g]) in the atmosphere. Measurements and calculations have shown that a secondary peak in the ozone density often exists in the middle atmosphere. A model has been developed to infer the ozone profile in the middle atmosphere by simultaneously solving the time-dependent chemistry of the molecular oxygen atmospheric and atmospheric-IR bands and O(ID) during twilight. Calculations are presented which show the effect of a secondary peak in the ozone density at various heights on the O[sub 2]([sup 1][Delta][sub g]) (0,1) band emission rate during twilight. The model is used to demonstrate that the London measurements are consistent with an ozone profile with a secondary peak at 85-90 km. 17 refs., 7 figs.

  7. Chemistry of Atmospheric Brown Carbon Alexander Laskin,*,

    E-Print Network [OSTI]

    Nizkorodov, Sergey

    Chemistry of Atmospheric Brown Carbon Alexander Laskin,*, Julia Laskin,*, and Sergey A. Nizkorodov fraction of atmospheric aerosol and has profound effects on air quality, atmospheric chemistry, and climate of radiation through Earth's atmosphere. The cloud albedo effect, Special Issue: 2015 Chemistry in Climate

  8. Aerosol Characterization Data from the Asian Pacific Regional Aerosol Characterization Project (ACE-Asia)

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    The Aerosol Characterization Experiments (ACE) were designed to increase understanding of how atmospheric aerosol particles affect the Earth's climate system. These experiments integrated in-situ measurements, satellite observations, and models to reduce the uncertainty in calculations of the climate forcing due to aerosol particles and improve the ability of models to predict the influences of aerosols on the Earth's radiation balance. ACE-Asia was the fourth in a series of experiments organized by the International Global Atmospheric Chemistry (IGAC) Program (A Core Project of the International Geosphere Biosphere Program). The Intensive Field Phase for ACE-Asia took place during the spring of 2001 (mid-March through early May) off the coast of China, Japan and Korea. ACE-Asia pursued three specific objectives: 1) Determine the physical, chemical, and radiative properties of the major aerosol types in the Eastern Asia and Northwest Pacific region and investigate the relationships among these properties. 2) Quantify the physical and chemical processes controlling the evolution of the major aerosol types and in particular their physical, chemical, and radiative properties. 3) Develop procedures to extrapolate aerosol properties and processes from local to regional and global scales, and assess the regional direct and indirect radiative forcing by aerosols in the Eastern Asia and Northwest Pacific region [Edited and shortened version of summary at http://data.eol.ucar.edu/codiac/projs?ACE-ASIA]. The Ace-Asia collection contains 174 datasets.

  9. Reduction of photosynthetically active radiation under extreme stratospheric-aerosol loads

    SciTech Connect (OSTI)

    Gerstl, S.A.W.; Zardecki, A.

    1981-01-01

    The recently published hypothesis that the Cretaceous-Tertiary extinctions might be caused by an obstruction of sunlight is tested by model calculations. First we compute the total mass of stratospheric aerosols under normal atmospheric conditions for four different (measured) aerosol size distributions and vertical profiles. For comparison, the stratospheric dust masses after four volcanic eruptions are also evaluated. Detailed solar radiative transfer calculations are then performed for artificially increased aerosol amounts until the postulated darkness scenario is obtained. Thus we find that a total stratospheric aerosol mass between 1 and 4 times 10/sup 16/ g is sufficient to reduce photosynthesis to 10/sup 3/ of normal. We also infer from this result that the impact of a 0.4- to 3-km-diameter asteroid or a close encounter with a Halley-size comet may deposit that amount of particulates into the stratosphere. The darkness scenario of Alvarez et al., is thus shown to be a possible extinction mechanism, even with smaller size asteroids or comets than previously estimated.

  10. WRF-Chem Simulations of Aerosols and Anthropogenic Aerosol Radiative Forcing in East Asia

    SciTech Connect (OSTI)

    Gao, Yi; Zhao, Chun; Liu, Xiaohong; Zhang, Meigen; Leung, Lai-Yung R.

    2014-08-01

    This study aims to provide a first comprehensive evaluation of WRF-Chem for modeling aerosols and anthropogenic aerosol radiative forcing (RF) over East Asia. Several numerical experiments were conducted from November 2007 to December 2008. Comparison between model results and observations shows that the model can generally reproduce the observed spatial distributions of aerosol concentration, aerosol optical depth (AOD) and single scattering albedo (SSA) from measurements at different sites, including the relatively higher aerosol concentration and AOD over East China and the relatively lower AOD over Southeast Asia, Korean, and Japan. The model also depicts the seasonal variation and transport of pollutions over East Asia. Particulate matter of 10 um or less in the aerodynamic diameter (PM10), black carbon (BC), sulfate (SO42-), nitrate (NO3-) and ammonium (NH4+) concentrations are higher in spring than other seasons in Japan due to the pollutant transport from polluted area of East Asia. AOD is high over Southwest and Central China in winter, spring and autumn and over North China in summer while is low over South China in summer due to monsoon precipitation. SSA is lowest in winter and highest in summer. The model also captures the dust events at the Zhangye site in the semi-arid region of China. Anthropogenic aerosol RF is estimated to range from -5 to -20 W m-2 over land and -20 to -40 W m-2 over ocean at the top of atmosphere (TOA), 5 to 30 W m-2 in the atmosphere (ATM) and -15 to -40 W m-2 at the bottom (BOT). The warming effect of anthropogenic aerosol in ATM results from BC aerosol while the negative aerosol RF at TOA is caused by scattering aerosols such as SO4 2-, NO3 - and NH4+. Positive BC RF at TOA compensates 40~50% of the TOA cooling associated with anthropogenic aerosol.

  11. Absorbing Aerosol Index (AAI) The residue method for the detection of aerosols

    E-Print Network [OSTI]

    Graaf, Martin de

    and calculation Main sensitivities of residue Problems with the residue Conclusions and outlook #12;#12;o = 380 scattering and absorption #12;#12;#12;Nadir View Solar zenith angle = 45o Residue = 3.5 Rayleigh atmosphere View Solar zenith angle = 45o Residue = -1.0 Rayleigh atmosphere, As = 0.16 Scattering aerosol layer

  12. A New Photochemistry Code for Terrestrial Exoplanet Atmospheres

    E-Print Network [OSTI]

    Johnson, Robert E.

    A New Photochemistry Code for Terrestrial Exoplanet Atmospheres Renyu Hu, Sara Seager Massachusetts-transport equation for 111 molecules and aerosols · Eddy diffusion · Chemical kinetics · Photolysis · Boundary

  13. Atmospheric optical calibration system

    DOE Patents [OSTI]

    Hulstrom, Roland L. (Bloomfield, CO); Cannon, Theodore W. (Golden, CO)

    1988-01-01

    An atmospheric optical calibration system is provided to compare actual atmospheric optical conditions to standard atmospheric optical conditions on the basis of aerosol optical depth, relative air mass, and diffuse horizontal skylight to global horizontal photon flux ratio. An indicator can show the extent to which the actual conditions vary from standard conditions. Aerosol scattering and absorption properties, diffuse horizontal skylight to global horizontal photon flux ratio, and precipitable water vapor determined on a real-time basis for optical and pressure measurements are also used to generate a computer spectral model and for correcting actual performance response of a photovoltaic device to standard atmospheric optical condition response on a real-time basis as the device is being tested in actual outdoor conditions.

  14. Atmospheric optical calibration system

    DOE Patents [OSTI]

    Hulstrom, R.L.; Cannon, T.W.

    1988-10-25

    An atmospheric optical calibration system is provided to compare actual atmospheric optical conditions to standard atmospheric optical conditions on the basis of aerosol optical depth, relative air mass, and diffuse horizontal skylight to global horizontal photon flux ratio. An indicator can show the extent to which the actual conditions vary from standard conditions. Aerosol scattering and absorption properties, diffuse horizontal skylight to global horizontal photon flux ratio, and precipitable water vapor determined on a real-time basis for optical and pressure measurements are also used to generate a computer spectral model and for correcting actual performance response of a photovoltaic device to standard atmospheric optical condition response on a real-time basis as the device is being tested in actual outdoor conditions. 7 figs.

  15. Aerosol-Cloud interactions : a new perspective in precipitation enhancement

    E-Print Network [OSTI]

    Gunturu, Udaya Bhaskar

    2010-01-01

    Increased industrialization and human activity modified the atmospheric aerosol composition and size-distribution during the last several decades. This has affected the structure and evolution of clouds, and precipitation ...

  16. Cloud-Driven Changes in Aerosol Optical Properties - Final Technical Report

    SciTech Connect (OSTI)

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

    2007-09-30

    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.

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

    SciTech Connect (OSTI)

    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.

  18. Formation of ozone and growth of aerosols in young smoke plumes from biomass burning

    E-Print Network [OSTI]

    Alvarado, Matthew James

    2008-01-01

    The combustion of biomass is a major source of atmospheric trace gases and aerosols. Regional and global-scale models of atmospheric chemistry and climate take estimates for these emissions and arbitrarily "mix" them into ...

  19. Surface organization of aqueous MgCl2 and application to atmospheric marine

    E-Print Network [OSTI]

    Surface organization of aqueous MgCl2 and application to atmospheric marine aerosol chemistry Nadia) Inorganic salts in marine aerosols play an active role in atmospheric chemistry, particularly in coastalCl2 surfaces as models of marine aerosol. Spectroscopy results reveal that the disturbance

  20. MEASUREMENT BASED DETERMINATION OF AEROSOL FORCINGS AT ARM SITES: PROPOSED JOINT ASP-ARM STUDY

    E-Print Network [OSTI]

    MEASUREMENT BASED DETERMINATION OF AEROSOL FORCINGS AT ARM SITES: PROPOSED JOINT ASP-ARM STUDY Stephen E. Schwartz For presentation at the Atmospheric Radiation Measurement (ARM) Program Science Team) Atmospheric Radiation Measurement (ARM) Southern Great Plains (SGP) site. There are numerous aerosol forcings

  1. Atmospheric Chemistry and Air Pollution

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Gaffney, Jeffrey S.; Marley, Nancy A.

    2003-01-01

    Atmospheric chemistry is an important discipline for understanding air pollution and its impacts. This mini-review gives a brief history of air pollution and presents an overview of some of the basic photochemistry involved in the production of ozone and other oxidants in the atmosphere. Urban air quality issues are reviewed with a specific focus on ozone and other oxidants, primary and secondary aerosols, alternative fuels, and the potential for chlorine releases to amplify oxidant chemistry in industrial areas. Regional air pollution issues such as acid rain, long-range transport of aerosols and visibility loss, and the connections of aerosols to ozonemore »and peroxyacetyl nitrate chemistry are examined. Finally, the potential impacts of air pollutants on the global-scale radiative balances of gases and aerosols are discussed briefly.« less

  2. Tethered balloon-based soundings of ozone, aerosols, and solar radiation near Mexico City during MIRAGE-MEX

    E-Print Network [OSTI]

    Greenberg, JP; Guenther, AB; Turnipseed, A

    2009-01-01

    ozone, aerosols, and solar radiation near Mexico City duringand solar radiation in the atmospheric boundary layer on the northern edge of Mexico

  3. Tethered balloon-based soundings of ozone, aerosols, and solar radiation near Mexico City during MIRAGE-MEX

    E-Print Network [OSTI]

    Greenberg, JP; Guenther, AB; Turnipseed, A

    2009-01-01

    ozone, aerosols, and solar radiation near Mexico City duringsolar radiation in the atmospheric boundary layer on the northern edge of Mexico

  4. Aerosol mobility size spectrometer

    DOE Patents [OSTI]

    Wang, Jian (Port Jefferson, NY); Kulkarni, Pramod (Port Jefferson Station, NY)

    2007-11-20

    A device for measuring aerosol size distribution within a sample containing aerosol particles. The device generally includes a spectrometer housing defining an interior chamber and a camera for recording aerosol size streams exiting the chamber. The housing includes an inlet for introducing a flow medium into the chamber in a flow direction, an aerosol injection port adjacent the inlet for introducing a charged aerosol sample into the chamber, a separation section for applying an electric field to the aerosol sample across the flow direction and an outlet opposite the inlet. In the separation section, the aerosol sample becomes entrained in the flow medium and the aerosol particles within the aerosol sample are separated by size into a plurality of aerosol flow streams under the influence of the electric field. The camera is disposed adjacent the housing outlet for optically detecting a relative position of at least one aerosol flow stream exiting the outlet and for optically detecting the number of aerosol particles within the at least one aerosol flow stream.

  5. STATUS OF THE BROADBAND HEATING RATE PROFILE (BBHRP) VAP Mlawer, E., Clough, S., and Delamere, J., Atmospheric and Environmental Research, Inc.

    E-Print Network [OSTI]

    STATUS OF THE BROADBAND HEATING RATE PROFILE (BBHRP) VAP Mlawer, E., Clough, S., and Delamere, J.bnl.gov ABSTRACT The Broadband Heating Rate Profile (BBHRP) VAP is a collaborative effort of all ARM Working Groups spatial/temporal scales; and b) produce a dataset of computed heating rates profiles for use by the Cloud

  6. Solid aerosol generator

    DOE Patents [OSTI]

    Prescott, D.S.; Schober, R.K.; Beller, J.

    1992-03-17

    An improved solid aerosol generator used to produce a gas borne stream of dry, solid particles of predetermined size and concentration is disclosed. The improved solid aerosol generator nebulizes a feed solution of known concentration with a flow of preheated gas and dries the resultant wet heated aerosol in a grounded, conical heating chamber, achieving high recovery and flow rates. 2 figs.

  7. Improved solid aerosol generator

    DOE Patents [OSTI]

    Prescott, D.S.; Schober, R.K.; Beller, J.

    1988-07-19

    An improved solid aerosol generator used to produce a gas borne stream of dry, solid particles of predetermined size and concentration. The improved solid aerosol generator nebulizes a feed solution of known concentration with a flow of preheated gas and dries the resultant wet heated aerosol in a grounded, conical heating chamber, achieving high recovery and flow rates. 2 figs.

  8. Atmospheric Aerosols and Cloud Condensation Nuclei

    E-Print Network [OSTI]

    Delene, David J.

    Vapor Pressure Ambient Vapor Pressure Top Plate Temperature = 297 K Bottom Plate Temperature = 292 K Maximum Supersautration = 1.0% Vapor Pressure ­ Ambient vapor pressure is linear from top to bottom. ­ Saturation vapor pressure is a curve from top to bottom. ­ A supersaturation exists between top and bottom

  9. Toxicity of atmospheric aerosols on marine phytoplankton

    E-Print Network [OSTI]

    2009-01-01

    the European and African aero- sols. Although the Africanblack bars) and European aero- sols (white bars) collectedpreindustrial and contemporary aero- sol Cu deposition

  10. Composition and Reactions of Atmospheric Aerosol Particles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    STXM measurements near the carbon absorption K edge at ALS Beamlines 7.0.1 and 5.3.2 in a helium-filled sample chamber maintained at 1 atm. X-ray transmission images, typically...

  11. Toxicity of atmospheric aerosols on marine phytoplankton

    E-Print Network [OSTI]

    2009-01-01

    fertilization on carbon sequestration in the Southern Ocean.production, and carbon sequestration (4–7). In areas whereproductivity and carbon sequestration and thus influence

  12. Composition and Reactions of Atmospheric Aerosol Particles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration would like submit the following commentsMethods forPortal

  13. Composition and Reactions of Atmospheric Aerosol Particles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration would like submit the following commentsMethods forPortalComposition and Reactions of

  14. Composition and Reactions of Atmospheric Aerosol Particles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration would like submit the following commentsMethods forPortalComposition and Reactions

  15. Composition and Reactions of Atmospheric Aerosol Particles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration would like submit the following commentsMethods forPortalComposition and

  16. Composition and Reactions of Atmospheric Aerosol Particles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity ofkandz-cm11 Outreach Home Room News PublicationsAuditsCluster Compatibilitydefault Changes from TukeyCryogenic

  17. Composition and Reactions of Atmospheric Aerosol Particles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity ofkandz-cm11 Outreach Home Room News PublicationsAuditsCluster Compatibilitydefault Changes from TukeyCryogenicComposition and

  18. Emerging Technology for Measuring Atmospheric Aerosol Properties

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration would like submitKansas NuclearElectronic StructureEly M. Gelbard,SevenEconomic Methodologyfor

  19. Carbonaceous aerosol particles from common vegetation in the Grand Canyon

    SciTech Connect (OSTI)

    Hallock, K.A.; Mazurek, M.A. (Brookhaven National Lab., Upton, NY (United States)); Cass, G.R. (California Inst. of Tech., Pasadena, CA (United States). Dept. of Environmental Engineering Science)

    1992-05-01

    The problem of visibility reduction in the Grand Canyon due to fine organic aerosol particles in the atmosphere has become an area of increased environmental concern. Aerosol particles can be derived from many emission sources. In this report, we focus on identifying organic aerosols derived from common vegetation in the Grand Canyon. These aerosols are expected to be significant contributors to the total atmospheric organic aerosol content. Aerosol samples from living vegetation were collected by resuspension of surface wax and resin components liberated from the leaves of vegetation common to areas of the Grand Canyon. The samples were analyzed using high-resolution gas chromatography/mass spectrometry (GC/MS). Probable identification of compounds was made by comparison of sample spectra with National Institute of Standards and Technology (NIST) mass spectral references and positive identification of compounds was made when possible by comparison with authentic standards as well as NIST references. Using these references, we have been able to positively identify the presence of n-alkane and n-alkanoic acid homolog series in the surface waxes of the vegetation sampled. Several monoterpenes, sesquiterpenes, and diterpenes were identified also as possible biogenic aerosols which may contribute to the total organic aerosol abundance leading to visibility reduction in the Grand Canyon.

  20. AEROSOL CHEMICAL COMPOSITION CHARACTERIZATION AT THE ARM SOUTHERN GREAT PLAINS (SGP) SITE USING AN AEROSOL CHEMICAL

    E-Print Network [OSTI]

    ) was integrated into the Aerosol Observing System (AOS) at the Atmospheric Radiation Measurement (ARM) SGP site in Oklahoma in Nov 2010. This instrument has been measuring concentrations of sulfate, ammonium, nitrate of oxygenated OA with minor contributions from hydrocarbon-like OA, indicating that the OA at the SGP site

  1. Aerosol Science and Technology, 43:486501, 2009 Copyright American Association for Aerosol Research

    E-Print Network [OSTI]

    a NOAA research vessel during the Texas Air Quality Study 2006/Gulf of Mexico Atmospheric Composition for glutaric acid in mixed glutaric acid/NH4HSO4 test aerosols was 0.22 ng collected mass, which corresponds min­1. During TexAQS 2006/GoMACCS, signals well above the detection limit were observed at a number

  2. Phase of atmospheric secondary organic material affects its reactivity

    E-Print Network [OSTI]

    of the reactivity of atmospheric SOM particles. atmospheric chemistry chemical aging organic aerosol collectionPhase of atmospheric secondary organic material affects its reactivity Mikinori Kuwata and Scot T of atmospheric organic particles among solid, semisolid, and liquid phases is of keen current scientific interest

  3. Predicted change in global secondary organic aerosol concentrations in response to future climate, emissions, and land use change

    E-Print Network [OSTI]

    Heald, C. L.; Henze, D. K.; Horowitz, L. W.; Feddema, Johannes J.; Lamarque, J. F.; Guenther, A.; Hess, P. G.; Vitt, F.; Seinfeld, J. H.; Goldstein, A. H.; Fung, I.

    2008-03-01

    The sensitivity of secondary organic aerosol (SOA) concentration to changes in climate and emissions is investigated using a coupled global atmosphere-land model driven by the year 2100 IPCC A1B scenario predictions. The Community Atmosphere Model...

  4. South African night sky brightness during high aerosol epochs

    E-Print Network [OSTI]

    Winkler, Hartmut; Marang, Fred

    2014-01-01

    Sky conditions in the remote, dry north-western interior of South Africa are now the subject of considerable interest in view of the imminent construction of numerous solar power plants in this area. Furthermore, the part of this region in which the core of the SKA is to be located (which includes SALT) has been declared an Astronomical Advantage Zone, for which sky brightness monitoring will now be mandatory. In this project we seek to characterise the sky brightness profile under a variety of atmospheric conditions. Key factors are of course the lunar phase and altitude, but in addition the sky brightness is also significantly affected by the atmospheric aerosol loading, as that influences light beam scattering. In this paper we chose to investigate the sky characteristics soon after the Mount Pinatubo volcanic eruption in 1991, which resulted in huge ash masses reaching the stratosphere (where they affected solar irradiance for several years). We re-reduced photometric sky measurements from the South Afric...

  5. ARESE (ARM Enhanced Shortwave Experiment) Science Plan [Atmospheric Radiation Program

    SciTech Connect (OSTI)

    Valero, F.P.J.; Schwartz, S.E.; Cess, R.D.; Ramanathan, V.; Collins, W.D.; Minnis, P.; Ackerman, T.P.; Vitko, J.; Tooman, T.P.

    1995-09-27

    Several recent studies have indicated that cloudy atmospheres may absorb significantly more solar radiation than currently predicted by models. The magnitude of this excess atmospheric absorption, is about 50% more than currently predicted and would have major impact on our understanding of atmospheric heating. Incorporation of this excess heating into existing general circulation models also appears to ameliorate some significant shortcomings of these models, most notably a tendency to overpredict the amount of radiant energy going into the oceans and to underpredict the tropopause temperature. However, some earlier studies do not show this excess absorption and an underlying physical mechanism that would give rise to such absorption has yet to be defined. Given the importance of this issue, the Department of Energy's (DOE) Atmospheric Radiation Measurement (ARM) program is sponsoring the ARM Enhanced Shortwave Experiment (ARESE) to study the absorption of solar radiation by clear and cloudy atmospheres. The experimental results will be compared with model calculations. Measurements will be conducted using three aircraft platforms (ARM-UAV Egrett, NASA ER-2, and an instrumented Twin Otter), as well as satellites and the ARM central and extended facilities in North Central Oklahoma. The project will occur over a four week period beginning in late September, 1995. Spectral broadband, partial bandpass, and narrow bandpass (10nm) solar radiative fluxes will be measured at different altitudes and at the surface with the objective to determine directly the magnitude and spectral characteristics of the absorption of shortwave radiation by the atmosphere (clear and cloudy). Narrow spectral channels selected to coincide with absorption by liquid water and ice will help in identifying the process of absorption of radiation. Additionally, information such as water vapor profiles, aerosol optical depths, cloud structure and ozone profiles, needed to use as input in radiative transfer calculations, will be acquired using the aircraft and surface facilities available to ARESE. This document outlines the scientific approach and measurement requirements of the project.

  6. Aerosol source term in high pressure melt ejection

    SciTech Connect (OSTI)

    Brockmann, J.E.; Tarbell, W.W.

    1984-11-01

    Pressurized ejection of melt from a reactor pressure vessel has been identified as an important element of a severe reactor accident. Copious aerosol production is observed when thermitically generated melts pressurized with nitrogen or carbon dioxide to 1.3 to 17 MPa are ejected into an air atmosphere. Aerosol particle size distributions measured in the tests have modes of about 0.5, 5, and > 10 ..mu..m. Mechanisms leading to formation of these multimodal size distributions are suggested. This aerosol is a potentially important fission product source term that has not been considered in previous severe accident analyses.

  7. Limited effect of anthropogenic nitrogen oxides on secondary organic aerosol formation

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Zheng, Y.; Unger, N.; Hodzic, A.; Emmons, L.; Knote, C.; Tilmes, S.; Lamarque, J.-F.; Yu, P.

    2015-12-08

    Globally, secondary organic aerosol (SOA) is mostly formed from emissions of biogenic volatile organic compounds (VOCs) by vegetation, but it can be modified by human activities as demonstrated in recent research. Specifically, nitrogen oxides (NOx = NO + NO2) have been shown to play a critical role in the chemical formation of low volatility compounds. We have updated the SOA scheme in the global NCAR (National Center for Atmospheric Research) Community Atmospheric Model version 4 with chemistry (CAM4-chem) by implementing a 4-product volatility basis set (VBS) scheme, including NOx-dependent SOA yields and aging parameterizations. Small differences are found for themore »no-aging VBS and 2-product schemes; large increases in SOA production and the SOA-to-OA ratio are found for the aging scheme. The predicted organic aerosol amounts capture both the magnitude and distribution of US surface annual mean measurements from the Interagency Monitoring of Protected Visual Environments (IMPROVE) network by 50 %, and the simulated vertical profiles are within a factor of 2 compared to aerosol mass spectrometer (AMS) measurements from 13 aircraft-based field campaigns across different regions and seasons. We then perform sensitivity experiments to examine how the SOA loading responds to a 50 % reduction in anthropogenic nitric oxide (NO) emissions in different regions. We find limited SOA reductions of 0.9–5.6, 6.4–12.0 and 0.9–2.8 % for global, southeast US and Amazon NOx perturbations, respectively. The fact that SOA formation is almost unaffected by changes in NOx can be largely attributed to a limited shift in chemical regime, to buffering in chemical pathways (low- and high-NOx pathways, O3 versus NO3-initiated oxidation) and to offsetting tendencies in the biogenic versus anthropogenic SOA responses.« less

  8. Broadband Heating Rate Profile Project (BBHRP) - SGP ripbe1mcfarlane

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Riihimaki, Laura; Shippert, Timothy

    The objective of the ARM Broadband Heating Rate Profile (BBHRP) Project is to provide a structure for the comprehensive assessment of our ability to model atmospheric radiative transfer for all conditions. Required inputs to BBHRP include surface albedo and profiles of atmospheric state (temperature, humidity), gas concentrations, aerosol properties, and cloud properties. In the past year, the Radiatively Important Parameters Best Estimate (RIPBE) VAP was developed to combine all of the input properties needed for BBHRP into a single gridded input file. Additionally, an interface between the RIPBE input file and the RRTM was developed using the new ARM integrated software development environment (ISDE) and effort was put into developing quality control (qc) flags and provenance information on the BBHRP output files so that analysis of the output would be more straightforward. This new version of BBHRP, sgp1bbhrpripbeC1.c1, uses the RIPBE files as input to RRTM, and calculates broadband SW and LW fluxes and heating rates at 1-min resolution using the independent column approximation. The vertical resolution is 45 m in the lower and middle troposphere to match the input cloud properties, but is at coarser resolution in the upper atmosphere. Unlike previous versions, the vertical grid is the same for both clear-sky and cloudy-sky calculations.

  9. Broadband Heating Rate Profile Project (BBHRP) - SGP ripbe370mcfarlane

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Riihimaki, Laura; Shippert, Timothy

    The objective of the ARM Broadband Heating Rate Profile (BBHRP) Project is to provide a structure for the comprehensive assessment of our ability to model atmospheric radiative transfer for all conditions. Required inputs to BBHRP include surface albedo and profiles of atmospheric state (temperature, humidity), gas concentrations, aerosol properties, and cloud properties. In the past year, the Radiatively Important Parameters Best Estimate (RIPBE) VAP was developed to combine all of the input properties needed for BBHRP into a single gridded input file. Additionally, an interface between the RIPBE input file and the RRTM was developed using the new ARM integrated software development environment (ISDE) and effort was put into developing quality control (qc) flags and provenance information on the BBHRP output files so that analysis of the output would be more straightforward. This new version of BBHRP, sgp1bbhrpripbeC1.c1, uses the RIPBE files as input to RRTM, and calculates broadband SW and LW fluxes and heating rates at 1-min resolution using the independent column approximation. The vertical resolution is 45 m in the lower and middle troposphere to match the input cloud properties, but is at coarser resolution in the upper atmosphere. Unlike previous versions, the vertical grid is the same for both clear-sky and cloudy-sky calculations.

  10. Broadband Heating Rate Profile Project (BBHRP) - SGP ripbe1mcfarlane

    SciTech Connect (OSTI)

    Riihimaki, Laura; Shippert, Timothy

    2014-11-05

    The objective of the ARM Broadband Heating Rate Profile (BBHRP) Project is to provide a structure for the comprehensive assessment of our ability to model atmospheric radiative transfer for all conditions. Required inputs to BBHRP include surface albedo and profiles of atmospheric state (temperature, humidity), gas concentrations, aerosol properties, and cloud properties. In the past year, the Radiatively Important Parameters Best Estimate (RIPBE) VAP was developed to combine all of the input properties needed for BBHRP into a single gridded input file. Additionally, an interface between the RIPBE input file and the RRTM was developed using the new ARM integrated software development environment (ISDE) and effort was put into developing quality control (qc) flags and provenance information on the BBHRP output files so that analysis of the output would be more straightforward. This new version of BBHRP, sgp1bbhrpripbeC1.c1, uses the RIPBE files as input to RRTM, and calculates broadband SW and LW fluxes and heating rates at 1-min resolution using the independent column approximation. The vertical resolution is 45 m in the lower and middle troposphere to match the input cloud properties, but is at coarser resolution in the upper atmosphere. Unlike previous versions, the vertical grid is the same for both clear-sky and cloudy-sky calculations.

  11. Broadband Heating Rate Profile Project (BBHRP) - SGP ripbe370mcfarlane

    SciTech Connect (OSTI)

    Riihimaki, Laura; Shippert, Timothy

    2014-11-05

    The objective of the ARM Broadband Heating Rate Profile (BBHRP) Project is to provide a structure for the comprehensive assessment of our ability to model atmospheric radiative transfer for all conditions. Required inputs to BBHRP include surface albedo and profiles of atmospheric state (temperature, humidity), gas concentrations, aerosol properties, and cloud properties. In the past year, the Radiatively Important Parameters Best Estimate (RIPBE) VAP was developed to combine all of the input properties needed for BBHRP into a single gridded input file. Additionally, an interface between the RIPBE input file and the RRTM was developed using the new ARM integrated software development environment (ISDE) and effort was put into developing quality control (qc) flags and provenance information on the BBHRP output files so that analysis of the output would be more straightforward. This new version of BBHRP, sgp1bbhrpripbeC1.c1, uses the RIPBE files as input to RRTM, and calculates broadband SW and LW fluxes and heating rates at 1-min resolution using the independent column approximation. The vertical resolution is 45 m in the lower and middle troposphere to match the input cloud properties, but is at coarser resolution in the upper atmosphere. Unlike previous versions, the vertical grid is the same for both clear-sky and cloudy-sky calculations.

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

    SciTech Connect (OSTI)

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

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

    SciTech Connect (OSTI)

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

    2010-04-09

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

  14. Pre-Cloud Aerosol, Cloud Droplet Concentration, and Cloud Condensation Nuclei from the VAMOS Ocean-Cloud-Atmosphere Land Study (VOCALS) Field Campaign First Quarter 2010 ASR Program Metric Report

    SciTech Connect (OSTI)

    Kleinman, LI; Springston, SR; Daum, PH; Lee, Y-N; Sedlacek, AJ; Senum, G; Wang, J

    2011-08-31

    In this, the first of a series of Program Metric Reports, we (1) describe archived data from the DOE G-1 aircraft, (2) illustrate several relations between sub-cloud aerosol, CCN, and cloud droplets pertinent to determining the effects of pollutant sources on cloud properties, and (3) post to the data archive an Excel spreadsheet that contains cloud and corresponding sub-cloud data.

  15. Thermophoretic separation of aerosol particles from a sampled gas stream

    DOE Patents [OSTI]

    Postma, Arlin K. (Halfway, OR)

    1986-01-01

    A method for separating gaseous samples from a contained atmosphere that includes aerosol particles uses the step of repelling particles from a gas permeable surface or membrane by heating the surface to a temperature greater than that of the surrounding atmosphere. The resulting thermophoretic forces maintain the gas permeable surface clear of aerosol particles. The disclosed apparatus utilizes a downwardly facing heated plate of gas permeable material to combine thermophoretic repulsion and gravity forces to prevent particles of any size from contacting the separating plate surfaces.

  16. Long-term impacts of aerosols on vertical development of cloud and precipitation

    SciTech Connect (OSTI)

    Li Z.; Liu Y.; Niu, F.; Fan, J.; Rosenfeld, D.; Ding, Y.

    2011-11-13

    Aerosols alter cloud density and the radiative balance of the atmosphere. This leads to changes in cloud microphysics and atmospheric stability, which can either suppress or foster the development of clouds and precipitation. The net effect is largely unknown, but depends on meteorological conditions and aerosol properties. Here, we examine the long-term impact of aerosols on the vertical development of clouds and rainfall frequencies, using a 10-year dataset of aerosol, cloud and meteorological variables collected in the Southern Great Plains in the United States. We show that cloud-top height and thickness increase with aerosol concentration measured near the ground in mixed-phase clouds-which contain both liquid water and ice-that have a warm, low base. We attribute the effect, which is most significant in summer, to an aerosol-induced invigoration of upward winds. In contrast, we find no change in cloud-top height and precipitation with aerosol concentration in clouds with no ice or cool bases. We further show that precipitation frequency and rain rate are altered by aerosols. Rain increases with aerosol concentration in deep clouds that have a high liquid-water content, but declines in clouds that have a low liquid-water content. Simulations using a cloud-resolving model confirm these observations. Our findings provide unprecedented insights of the long-term net impacts of aerosols on clouds and precipitation.

  17. Statistical analysis of aerosol species, trace gasses, and meteorology in Chicago

    E-Print Network [OSTI]

    O'Brien, Timothy E.

    ) and principal component analysis (PCA) were applied to atmospheric aerosol and trace gas concentrations and Schmeling 2006, 2007; Shen et al. 2009). The composition of aerosols is region-specific and encompasses inorganic and organic species of natural and anthropogenic ori- gin, present due to primary emission

  18. Mars aerosol studies with the MGS TES emission phase function observations: Optical depths, particle

    E-Print Network [OSTI]

    Whitney, Barbara A.

    aerosol properties to date. TES solar band and infrared (IR) spectral EPF sequences are analyzed to obtain and scattering of radiation; 6225 Planetology: Solar System Objects: Mars; KEYWORDS: Martian atmosphere, aerosols, radiative forcing from atmo- spheric dust solar absorption and thermal emission was recognized as a primary

  19. Measuring Nighttime Atmospheric Opacity Using Images From the Mars Exploration Rovers 

    E-Print Network [OSTI]

    Bean, Keri M

    2012-07-11

    Atmospheric opacity, otherwise known as optical depth, is the measurement of the amount of radiation reaching the surface through the atmosphere. The spatial and temporal patterns in optical depth tell us about the aerosol and cloud cycles...

  20. Contrasting the direct radiative effect and direct radiative forcing of aerosols

    E-Print Network [OSTI]

    Heald, Colette L.

    The direct radiative effect (DRE) of aerosols, which is the instantaneous radiative impact of all atmospheric particles on the Earth's energy balance, is sometimes confused with the direct radiative forcing (DRF), which ...

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

    E-Print Network [OSTI]

    Cziczo, Daniel James

    Substantial uncertainties still exist in the scientific understanding of the possible interactions between urban and natural (biogenic) emissions in the production and transformation of atmospheric aerosol and the resulting ...

  2. The role of aqueous-phase oxidation in the formation of highly-oxidized organic aerosol

    E-Print Network [OSTI]

    Daumit, Kelly Elizabeth

    2015-01-01

    Atmospheric particulate matter (or "aerosol") is known to have important implications for climate change, air quality, and human health. Our ability to predict its formation and fate is hindered by uncertainties associated ...

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

    SciTech Connect (OSTI)

    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.

  4. The Two-Column Aerosol Project (TCAP) Science Plan

    SciTech Connect (OSTI)

    Berkowitz, CM; Berg, LK; Cziczo, DJ; Flynn, CJ; Kassianov, EI; Fast, JD; Rasch, PJ; Shilling, JE; Zaveri, RA; Zelenyuk, A; Ferrare, RA; Hostetler, CA; Cairns, B; Russell, PB; Ervens, B

    2011-07-27

    The Two-Column Aerosol Project (TCAP) field campaign will provide a detailed set of observations with which to (1) perform radiative and cloud condensation nuclei (CCN) closure studies, (2) evaluate a new retrieval algorithm for aerosol optical depth (AOD) in the presence of clouds using passive remote sensing, (3) extend a previously developed technique to investigate aerosol indirect effects, and (4) evaluate the performance of a detailed regional-scale model and a more parameterized global-scale model in simulating particle activation and AOD associated with the aging of anthropogenic aerosols. To meet these science objectives, the Atmospheric Radiation Measurement (ARM) Climate Research Facility will deploy the ARM Mobile Facility (AMF) and the Mobile Aerosol Observing System (MAOS) on Cape Cod, Massachusetts, for a 12-month period starting in the summer of 2012 in order to quantify aerosol properties, radiation, and cloud characteristics at a location subject to both clear and cloudy conditions, and clean and polluted conditions. These observations will be supplemented by two aircraft intensive observation periods (IOPs), one in the summer and a second in the winter. Each IOP will deploy one, and possibly two, aircraft depending on available resources. The first aircraft will be equipped with a suite of in situ instrumentation to provide measurements of aerosol optical properties, particle composition and direct-beam irradiance. The second aircraft will fly directly over the first and use a multi-wavelength high spectral resolution lidar (HSRL) and scanning polarimeter to provide continuous optical and cloud properties in the column below.

  5. On the relationship between stratospheric aerosols and nitrogen dioxide

    SciTech Connect (OSTI)

    Mills, M.J.; Langford, A.O.; O'Leary, T.J.; Arpag, K.; Miller, H.L.; Proffitt, M.H.; Sanders, R.W.; Solomon, S. (Aeronomy Laboratory, NOAA, Boulder, CO (United States) Univ. of Colorado, Boulder (United States))

    1993-06-18

    The authors report measurements of stratospheric column abundances of nitrogen dioxide above the Colorado mountains during Jan, Feb, and Mar 1992, following the arrival of the aerosol loading injected by Mt. Pinatubo. The column abundance data was correlated with concurrent lidar measurements which provided vertical aerosol profiles at the same site. Chemical reactions within polar stratospheric clouds have been shown to play a major role in ozone chemistry in the polar regions, and one could ask whether such clouds at mid latitudes could play a similar role. The sulfur dioxide loading due to the volcanic eruption provides an abrupt increase in sulfuric acid aerosol surface area in mid latitude areas, providing a convenient test of this question. Column NO[sub 2] densities are observed to fall, but also found to saturate at a certain stratospheric aerosol density.

  6. Atmospheric Environment ] (

    E-Print Network [OSTI]

    Raman, Sethu

    that the influence of the urban region on wind patterns and atmospheric stability could be studied. HeightAtmospheric Environment ] (

  7. Speciation of Fe in ambient aerosol and cloudwater

    SciTech Connect (OSTI)

    Siefert, L. [California Institute of Technology, Pasadena, CA (United States)

    1996-08-15

    Atmospheric iron (Fe) is thought to play an important role in cloudwater chemistry (e.g., S(IV) oxidation, oxidant production, etc.), and is also an important source of Fe to certain regions of the worlds oceans where Fe is believed to be a rate-limiting nutrient for primary productivity. This thesis focuses on understanding the chemistry, speciation and abundance of Fe in cloudwater and aerosol in the troposphere, through observations of Fe speciation in the cloudwater and aerosol samples collected over the continental United States and the Arabian Sea. Different chemical species of atmospheric Fe were measured in aerosol and cloudwater samples to help assess the role of Fe in cloudwater chemistry.

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

    SciTech Connect (OSTI)

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

    2014-05-13

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

  9. RACORO aerosol data processing

    SciTech Connect (OSTI)

    Elisabeth Andrews

    2011-10-31

    The RACORO aerosol data (cloud condensation nuclei (CCN), condensation nuclei (CN) and aerosol size distributions) need further processing to be useful for model evaluation (e.g., GCM droplet nucleation parameterizations) and other investigations. These tasks include: (1) Identification and flagging of 'splash' contaminated Twin Otter aerosol data. (2) Calculation of actual supersaturation (SS) values in the two CCN columns flown on the Twin Otter. (3) Interpolation of CCN spectra from SGP and Twin Otter to 0.2% SS. (4) Process data for spatial variability studies. (5) Provide calculated light scattering from measured aerosol size distributions. Below we first briefly describe the measurements and then describe the results of several data processing tasks that which have been completed, paving the way for the scientific analyses for which the campaign was designed. The end result of this research will be several aerosol data sets which can be used to achieve some of the goals of the RACORO mission including the enhanced understanding of cloud-aerosol interactions and improved cloud simulations in climate models.

  10. Impact of anthropogenic absorbing aerosols on clouds and precipitation

    E-Print Network [OSTI]

    Impact of anthropogenic absorbing aerosols on clouds and precipitation: A review of recent and precipitation: A review of recent progresses Chien Wang Massachusetts Institute of Technology, E19-439K, 77 atmospheric circulation, and hence clouds and precipitation. Recent studies have suggested that the changes

  11. Aerosol Retrievals from ARM SGP MFRSR Data

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Alexandrov, Mikhail

    2008-01-15

    The Multi-Filter Rotating Shadowband Radiometer (MFRSR) makes precise simultaneous measurements of the solar direct normal and diffuse horizontal irradiances at six wavelengths (nominally 415, 500, 615, 673, 870, and 940 nm) at short intervals (20 sec for ARM instruments) throughout the day. Time series of spectral optical depth are derived from these measurements. Besides water vapor at 940 nm, the other gaseous absorbers within the MFRSR channels are NO2 (at 415, 500, and 615 nm) and ozone (at 500, 615, and 670 nm). Aerosols and Rayleigh scattering contribute atmospheric extinction in all MFRSR channels. Our recently updated MFRSR data analysis algorithm allows us to partition the spectral aerosol optical depth into fine and coarse modes and to retrieve the fine mode effective radius. In this approach we rely on climatological amounts of NO2 from SCIAMACHY satellite retrievals and use daily ozone columns from TOMS.

  12. Aerosol Retrievals from ARM SGP MFRSR Data

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Alexandrov, Mikhail

    The Multi-Filter Rotating Shadowband Radiometer (MFRSR) makes precise simultaneous measurements of the solar direct normal and diffuse horizontal irradiances at six wavelengths (nominally 415, 500, 615, 673, 870, and 940 nm) at short intervals (20 sec for ARM instruments) throughout the day. Time series of spectral optical depth are derived from these measurements. Besides water vapor at 940 nm, the other gaseous absorbers within the MFRSR channels are NO2 (at 415, 500, and 615 nm) and ozone (at 500, 615, and 670 nm). Aerosols and Rayleigh scattering contribute atmospheric extinction in all MFRSR channels. Our recently updated MFRSR data analysis algorithm allows us to partition the spectral aerosol optical depth into fine and coarse modes and to retrieve the fine mode effective radius. In this approach we rely on climatological amounts of NO2 from SCIAMACHY satellite retrievals and use daily ozone columns from TOMS.

  13. Limited effect of anthropogenic nitrogen oxides on Secondary Organic Aerosol formation

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Zheng, Y.; Unger, N.; Hodzic, A.; Emmons, L.; Knote, C.; Tilmes, S.; Lamarque, J.-F.; Yu, P.

    2015-08-28

    Globally, secondary organic aerosol (SOA) is mostly formed from emissions of biogenic volatile organic compounds (VOCs) by vegetation, but can be modified by human activities as demonstrated in recent research. Specifically, nitrogen oxides (NOx = NO + NO2) have been shown to play a critical role in the chemical formation of low volatility compounds. We have updated the SOA scheme in the global NCAR Community Atmospheric Model version 4 with chemistry (CAM4-chem) by implementing a 4-product Volatility Basis Set (VBS) scheme, including NOx-dependent SOA yields and aging parameterizations. The predicted organic aerosol amounts capture both the magnitude and distribution ofmore »US surface annual mean measurements from the Interagency Monitoring of Protected Visual Environments (IMPROVE) network by 50 %, and the simulated vertical profiles are within a factor of two compared to Aerosol Mass Spectrometer (AMS) measurements from 13 aircraft-based field campaigns across different region and seasons. We then perform sensitivity experiments to examine how the SOA loading responds to a 50 % reduction in anthropogenic nitric oxide (NO) emissions in different regions. We find limited SOA reductions of 0.9 to 5.6, 6.4 to 12.0 and 0.9 to 2.8 % for global, the southeast US and the Amazon NOx perturbations, respectively. The fact that SOA formation is almost unaffected by changes in NOx can be largely attributed to buffering in chemical pathways (low- and high-NOx pathways, O3 versus NO3-initiated oxidation) and to offsetting tendencies in the biogenic versus anthropogenic SOA responses.« less

  14. On modification of global warming by sulfate aerosols

    SciTech Connect (OSTI)

    Mitchell, J.F.B.; Johns, T.C.

    1997-02-01

    There is increasing evidence that the response of climate to increasing greenhouse gases may be modified by accompanying increases in sulfate aerosols. In this study, the patterns of response in the surface climatology of a coupled ocean-atmosphere general circulation model forced by increases in carbon dioxide alone is compared with those obtained by increasing carbon dioxide and aerosol forcing. The simulations are run from early industrial times using the estimated historical forcing and continued to the end of the twenty-first century assuming a nonintervention emissions scenario for greenhouse gases and aerosols. The comparison is made for the period 2030-2050 when the aerosol forcing is a maximum. In winter, the cooling due to aerosols merely tends to reduce the response to carbon dioxide, whereas in summer, it weakens the monsoon circulations and reverses some of the changes in the hydrological cycle on increasing carbon dioxide. This response is in some respects similar to that found in simulations with changed orbital parameters, as between today and the middle Holocene. The hydrological response in the palaeosimulations is supported by palaeoclimatic reconstructions. The results of changes in aerosol concentrations of the magnetic projected in the scenarios would have a major effect on regional climate, especially over Europe and Southeast Asia. 74 refs., 12 figs., 6 tabs.

  15. Aerosol collection characteristics of ambient aerosol samplers 

    E-Print Network [OSTI]

    Ortiz, Carlos A

    1978-01-01

    when the sampler is not in operation, both as functions of particle size and wind speed. Wind velocity was a major cause of bias for the four samplers when collecting aerosol particles & 10 um. Characteristic curves were very similar for the 0. 38 m... x 0. 38 m ( 15" x 15") Hi-Vol and the 0. 29 m x 0. 36 m (11&" x 14") Hi-Vol. At 28 um and wind speeds of 2, 8, and 24 km/hr, sampling effectiveness values respectively were 70, 43, and 43 percent for the 0. 38 m x 0. 38 m Hi-Vol and 81, 56, and 43...

  16. Thermophoretic separation of aerosol particles from a sampled gas stream

    DOE Patents [OSTI]

    Postma, A.K.

    1984-09-07

    This disclosure relates to separation of aerosol particles from gas samples withdrawn from within a contained atmosphere, such as containment vessels for nuclear reactors or other process equipment where remote gaseous sampling is required. It is specifically directed to separation of dense aerosols including particles of any size and at high mass loadings and high corrosivity. The United States Government has rights in this invention pursuant to Contract DE-AC06-76FF02170 between the US Department of Energy and Westinghouse Electric Corporation.

  17. Impacts of aerosols and clouds on photolysis frequencies and photochemistry during TRACE-P

    E-Print Network [OSTI]

    Clarke, Antony

    with the polluted air masses. The accumulated aerosol impact generally is to reduce O3 concentrations by about 6 Atmospheric Composition and Structure: Pollution--urban and regional (0305); 0365 Atmospheric Composition and Earth Science and Technology, University of Hawaii at Manoa, Honolulu, Hawaii, USA. 7 Department

  18. A reanalysis of carbonyl sulfide as a source of stratospheric background sulfur aerosol

    SciTech Connect (OSTI)

    Chin, M.; Davis, D.D. [Georgia Institute of Technology, Atlanta, GA (United States)] [Georgia Institute of Technology, Atlanta, GA (United States)

    1995-05-20

    The authors present an analysis of carbonyl sulfide (OCS) in the earth`s atmosphere, with the objective being to assess its role in the formation of sulfate aerosols in the stratosphere. They review the amount of OCS in the atmosphere, its distribution between the troposphere and stratosphere, the estimated source term for emission to the atmosphere, and from one-dimensional model calculations infer a stratospheric lifetime to photochemical reactions of ten years. Calculations infer a sulfur production rate from OCS oxidation which is a factor of 2 to 5 less than recent sulfur aerosol estimates would infer. They discuss a number of possible explanations for the discrepancy.

  19. Atmospheric Radiation Measurement (ARM) Data from Specific Instruments Used in the ARM Program

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    ARM is known for its comprehensive set of world-class, and in some cases, unique, instruments available for use by the global scientific community. In addition to the ARM instruments, the ARM Climate Research Facility identifies and acquires a wide variety of data including model, satellite, and surface data, from "external instruments," to augment the data being generated within the program. External instruments belong to organizations that are outside of the ARM Program. Field campaign instruments are another source of data used to augment routine observations. The huge archive of ARM data can be organized by instrument categories into twelve "collections:" Aerosols, Airborne Observations, Atmospheric Carbon, Atmospheric Profiling, Cloud Properties, Derived Quantities and Models, Ocean Observations, Radiometric, Satellite Observations, Surface Meteorology, Surface/Subsurface Properties, and Other. Clicking on one of the instrument categories leads to a page that breaks that category down into sub-categories. For example, "Atmospheric Profiling" is broken down into ARM instruments (with 11 subsets), External Instruments (with 6 subsets), and Field Campaign Instruments (with 42 subsets). Each of the subset links, in turn, leads to detailed information pages and links to specific data streams. Users will be requested to create a password, but the data files are free for viewing and downloading.

  20. Ganges Valley Aerosol Experiment: Science and Operations Plan

    SciTech Connect (OSTI)

    Kotamarthi, VR

    2010-06-21

    The Ganges Valley region is one of the largest and most rapidly developing sections of the Indian subcontinent. The Ganges River, which provides the region with water needed for sustaining life, is fed primarily by snow and rainfall associated with Indian summer monsoons. Impacts of changes in precipitation patterns, temperature, and the flow of the snow-fed rivers can be immense. Recent satellite-based measurements have indicated that the upper Ganges Valley has some of the highest persistently observed aerosol optical depth values. The aerosol layer covers a vast region, extending across the Indo-Gangetic Plain to the Bay of Bengal during the winter and early spring of each year. The persistent winter fog in the region is already a cause of much concern, and several studies have been proposed to understand the economic, scientific, and societal dimensions of this problem. During the INDian Ocean EXperiment (INDOEX) field studies, aerosols from this region were shown to affect cloud formation and monsoon activity over the Indian Ocean. This is one of the few regions showing a trend toward increasing surface dimming and enhanced mid-tropospheric warming. Increasing air pollution over this region could modify the radiative balance through direct, indirect, and semi-indirect effects associated with aerosols. The consequences of aerosols and associated pollution for surface insolation over the Ganges Valley and monsoons, in particular, are not well understood. The proposed field study is designed for use of (1) the ARM Mobile Facility (AMF) to measure relevant radiative, cloud, convection, and aerosol optical characteristics over mainland India during an extended period of 9–12 months and (2) the G-1 aircraft and surface sites to measure relevant aerosol chemical, physical, and optical characteristics in the Ganges Valley during a period of 6–12 weeks. The aerosols in this region have complex sources, including burning of coal, biomass, and biofuels; automobile emissions; and dust. The extended AMF deployment will enable measurements under different regimes of the climate and aerosol abundance—in the wet monsoon period with low aerosol loading; in the dry, hot summer with aerosols dispersed throughout the atmospheric column; and in the cool, dry winter with aerosols confined mostly to the boundary later and mid-troposphere. Each regime, in addition, has its own distinct radiative and atmospheric dynamic drivers. The aircraft operational phase will assist in characterizing the aerosols at times when they have been observed to be at the highest concentrations. A number of agencies in India will collaborate with the proposed field study and provide support in terms of planning, aircraft measurements, and surface sites. The high concentration of aerosols in the upper Ganges Valley, together with hypotheses involving several possible mechanisms with direct impacts on the hydrologic cycle of the region, gives us a unique opportunity to generate data sets that will be useful both in understanding the processes at work and in providing answers regarding the effects of aerosols on climate in a region where the perturbation is the highest.

  1. Broadband Heating Rate Profile Project (BBHRP) - SGP 1bbhrpripbe1mcfarlane

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Riihimaki, Laura; Shippert, Timothy

    The objective of the ARM Broadband Heating Rate Profile (BBHRP) Project is to provide a structure for the comprehensive assessment of our ability to model atmospheric radiative transfer for all conditions. Required inputs to BBHRP include surface albedo and profiles of atmospheric state (temperature, humidity), gas concentrations, aerosol properties, and cloud properties. In the past year, the Radiatively Important Parameters Best Estimate (RIPBE) VAP was developed to combine all of the input properties needed for BBHRP into a single gridded input file. Additionally, an interface between the RIPBE input file and the RRTM was developed using the new ARM integrated software development environment (ISDE) and effort was put into developing quality control (qc) flags and provenance information on the BBHRP output files so that analysis of the output would be more straightforward. This new version of BBHRP, sgp1bbhrpripbeC1.c1, uses the RIPBE files as input to RRTM, and calculates broadband SW and LW fluxes and heating rates at 1-min resolution using the independent column approximation. The vertical resolution is 45 m in the lower and middle troposphere to match the input cloud properties, but is at coarser resolution in the upper atmosphere. Unlike previous versions, the vertical grid is the same for both clear-sky and cloudy-sky calculations.

  2. Broadband Heating Rate Profile Project (BBHRP) - SGP 1bbhrpripbe1mcfarlane

    SciTech Connect (OSTI)

    Riihimaki, Laura; Shippert, Timothy

    2014-11-05

    The objective of the ARM Broadband Heating Rate Profile (BBHRP) Project is to provide a structure for the comprehensive assessment of our ability to model atmospheric radiative transfer for all conditions. Required inputs to BBHRP include surface albedo and profiles of atmospheric state (temperature, humidity), gas concentrations, aerosol properties, and cloud properties. In the past year, the Radiatively Important Parameters Best Estimate (RIPBE) VAP was developed to combine all of the input properties needed for BBHRP into a single gridded input file. Additionally, an interface between the RIPBE input file and the RRTM was developed using the new ARM integrated software development environment (ISDE) and effort was put into developing quality control (qc) flags and provenance information on the BBHRP output files so that analysis of the output would be more straightforward. This new version of BBHRP, sgp1bbhrpripbeC1.c1, uses the RIPBE files as input to RRTM, and calculates broadband SW and LW fluxes and heating rates at 1-min resolution using the independent column approximation. The vertical resolution is 45 m in the lower and middle troposphere to match the input cloud properties, but is at coarser resolution in the upper atmosphere. Unlike previous versions, the vertical grid is the same for both clear-sky and cloudy-sky calculations.

  3. People Profiles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    People Profiles Featured Profile Peter Thelin The art of optics Read More Lisa Burrows Lisa Burrows Jeremy Huckins Jeremy Huckins Ibo Matthews Ibo Matthews Susanna Reyes Susana...

  4. Relative Content of Black Carbon in Submicron Aerosol as a Sign of the Effect of Forest Fire Smokes

    SciTech Connect (OSTI)

    Kozlov, V.S.; Panchenko, M.V.; Yauscheva, E.P.

    2005-03-18

    Biomass burning occurs often in regions containing vast forest tracts and peat-bogs. These processes are accompanied by the emission of a large amount of aerosol particles and crystal carbon (black carbon [BC], soot). BC is the predominant source of solar absorption in atmospheric aerosol, which impacts climate. (Jacobson 2001; Rozenberg 1982). In this paper, we analyze the results of laboratory and field investigations that focused on the relative content of BC in aerosol particles. Main attention is given to the study of possibility using this parameter as an informative sign for estimating the effect of remote forest fire smokes on the near-ground aerosol composition.

  5. Aerosols and Clouds: In Cahoots to Change Climate

    ScienceCinema (OSTI)

    Berg, Larry

    2014-06-02

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

  6. Aerosols and Clouds: In Cahoots to Change Climate

    SciTech Connect (OSTI)

    Berg, Larry

    2014-03-29

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

  7. Maritime Aerosol Network as a component of Aerosol Robotic A. Smirnov,1,2

    E-Print Network [OSTI]

    Maritime Aerosol Network as a component of Aerosol Robotic Network A. Smirnov,1,2 B. N. Holben,2 I of the Maritime Aerosol Network (MAN), which has been developed as a component of the Aerosol Robotic Network), Maritime Aerosol Network as a component of Aerosol Robotic Network, J. Geophys. Res., 114, D06204, doi:10

  8. Parameterizations of Cloud Microphysics and Indirect Aerosol Effects

    SciTech Connect (OSTI)

    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, 2005]. Recently, a detailed spectral-bin microphysical scheme was implemented into the Goddard Cumulus Ensemble (GCE) model. Atmospheric aerosols are also described using number density size-distribution functions. A spectral-bin microphysical model is very expensive from a computational point of view and has only been implemented into the 2D version of the GCE at the present time. The model is tested by studying the evolution of deep tropical clouds in the west Pacific warm pool region and summertime convection over a mid-latitude continent with different concentrations of CCN: a low "clean" concentration and a high "dirty" concentration. The impact of atmospheric aerosol concentration on cloud and precipitation will be investigated. 2. MODEL DESCRIPTION AND CASE STUDIES 2.1 GCE MODEL The model used in this study is the 2D version of the GCE model. Modeled flow is anelastic. Second- or higher-order advection schemes can produce negative values in the solution. Thus, a Multi-dimensional Positive Definite Advection Transport Algorithm (MPDATA) has been implemented into the model. All scalar variables (potential temperature, water vapor, turbulent coefficient and all five hydrometeor classes) use forward time differencing and the MPDATA for advection. Dynamic variables, u, v and w, use a second-order accurate advection scheme and a leapfrog time integration (kinetic energy semi-conserving method). Short-wave (solar) and long-wave radiation as well as a subgrid-scale TKE turbulence scheme are also included in the model. Details of the model can be found in Tao and Simpson (1993) and Tao et al. (2003). 2.2 Microphysics (Bin Model) The formulation of the explicit spectral-bin microphysical processes is based on solving stochastic kinetic equations for the size distribution functions of water droplets (cloud droplets and raindrops), and six types of ice particles: pristine ice crystals (columnar and plate-like), snow (dendrites and aggregates), graupel and frozen drops/hail. Each type is described by a special size distribution function containing 33 categories (bin

  9. Aerosol Observing System (AOS) Handbook

    SciTech Connect (OSTI)

    Jefferson, A

    2011-01-17

    The Aerosol Observing System (AOS) is a suite of in situ surface measurements of aerosol optical and cloud-forming properties. The instruments measure aerosol properties that influence the earth’s radiative balance. The primary optical measurements are those of the aerosol scattering and absorption coefficients as a function of particle size and radiation wavelength and cloud condensation nuclei (CCN) measurements as a function of percent supersaturation. Additional measurements include those of the particle number concentration and scattering hygroscopic growth. Aerosol optical measurements are useful for calculating parameters used in radiative forcing calculations such as the aerosol single-scattering albedo, asymmetry parameter, mass scattering efficiency, and hygroscopic growth. CCN measurements are important in cloud microphysical models to predict droplet formation.

  10. Aerosol source term in high-pressure-melt ejection. [PWR; BWR

    SciTech Connect (OSTI)

    Brockmann, J.E.; Tarbell, W.W.

    1983-01-01

    Pressurized ejection of melt from a reactor pressure vessel has been identified as an important element of a severe reactor accident. Copious aerosol production is observed when thermitically generated melts pressurized with nitrogen or carbon dioxide to 1.3 to 17 MPa are ejected into an air atmosphere. Aerosol particle size distributions measured in the tests have modes of about 0.5, 5, and > 10..mu..m. Mechanisms leading to formation of these multimodal size distributions are suggested. This aerosol is a potentially important fission product source term which has not been considered in previous severe accident analyses.

  11. Aerosol specification in single-column CAM5

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Lebassi-Habtezion, B.; Caldwell, P.

    2014-11-17

    The ability to run a global climate model in single-column mode is very useful for testing model improvements because single-column models (SCMs) are inexpensive to run and easy to interpret. A major breakthrough in Version 5 of the Community Atmosphere Model (CAM5) is the inclusion of prognostic aerosol. Unfortunately, this improvement was not coordinated with the SCM version of CAM5 and as a result CAM5-SCM initializes aerosols to zero. In this study we explore the impact of running CAM5-SCM with aerosol initialized to zero (hereafter named Default) and test three potential fixes. The first fix is to use CAM5'smore »prescribed aerosol capability, which specifies aerosols at monthly climatological values. The second method is to prescribe aerosols at observed values. The third approach is to fix droplet and ice crystal numbers at prescribed values. We test our fixes in four different cloud regimes to ensure representativeness: subtropical drizzling stratocumulus (based on the DYCOMS RF02 case study), mixed-phase Arctic stratocumulus (using the MPACE-B case study), tropical shallow convection (using the RICO case study), and summertime mid-latitude continental convection (using the ARM95 case study). Stratiform cloud cases (DYCOMS RF02 and MPACE-B) were found to have a strong dependence on aerosol concentration, while convective cases (RICO and ARM95) were relatively insensitive to aerosol specification. This is perhaps expected because convective schemes in CAM5 do not currently use aerosol information. Adequate liquid water content in the MPACE-B case was only maintained when ice crystal number concentration was specified because the Meyers et al. (1992) deposition/condensation ice nucleation scheme used by CAM5 greatly overpredicts ice nucleation rates, causing clouds to rapidly glaciate. Surprisingly, predicted droplet concentrations for the ARM95 region in both SCM and global runs were around 25 cm?3, which is much lower than observed. This finding suggests that CAM5 has problems capturing aerosol effects in this climate regime.« less

  12. Aerosols and their influence on radiation partitioning and savanna productivity in northern Australia

    SciTech Connect (OSTI)

    Kanniah, K. D.; Beringer, J.; Tapper, N. J.; Long, Charles N.

    2010-05-01

    We investigated the effect of aerosols and clouds on the Net Ecosystem Productivity (NEP) of savannas in northern Australia using aerosol optical depth, clouds and radiation data from the Atmospheric Radiation Measurement (ARM) site in Darwin and carbon flux data measured from eddy covariance techniques from a site at Howard Springs, 35km southeast of Darwin. Generally we found that the concentration of aerosols in this region was relatively low than observed at other sites, therefore the proportion of diffuse radiation reaching the earths surface was only ~ 30%. As a result, we observed only a modest change in carbon uptake under aerosol laden skies and there was no significant difference for dry season Radiation Use Efficiency (RUE) between clear sky, aerosols or thin clouds. On the other hand thick clouds in the wet season produce much more diffuse radiation than aerosols or thin clouds and therefore the initial canopy quantum efficiency was seen to increase 45 and 2.5 times more than under thin clouds and aerosols respectively. The normalized carbon uptake under thick clouds is 57% and 50% higher than under aerosols and thin clouds respectively even though the total irradiance received under thick clouds was reduced 59% and 50% than under aerosols and thin clouds respectively. However, reduction in total irradiance decreases the mean absolute carbon uptake as much as 22% under heavy cloud cover compared to thin clouds or aerosols. Thus, any increase in aerosol concentration or cloud cover that can enhance the diffuse component may have large impacts on productivity in this region.

  13. Revised for Journal of Atmospheric and Oceanic Technology Dec. 18, 2001 DO NOT QUOTE OR CIRCULATE

    E-Print Network [OSTI]

    Clarke, Antony

    of Hawaii, Honolulu, HI *Department of Atmospheric Sciences, University of Washington, Seattle, WA #12 studies of atmospheric pollution, atmospheric chemistry, aerosol radiative effects on climate, visibility etc. Hence in-situ measurements in minimally disturbed air are desirable for many applications

  14. A Study of Cloud Processing of Organic Aerosols Using Models and CHAPS Data

    SciTech Connect (OSTI)

    Ervens, Barbara

    2012-01-17

    The main theme of our work has been the identification of parameters that mostly affect the formation and modification of aerosol particles and their interaction with water vapor. Our detailed process model studies led to simplifications/parameterizations of these effects that bridge detailed aerosol information from laboratory and field studies and the need for computationally efficient expressions in complex atmospheric models. One focus of our studies has been organic aerosol mass that is formed in the atmosphere by physical and/or chemical processes (secondary organic aerosol, SOA) and represents a large fraction of atmospheric particulate matter. Most current models only describe SOA formation by condensation of low volatility (or semivolatile) gas phase products and neglect processes in the aqueous phase of particles or cloud droplets that differently affect aerosol size and vertical distribution and chemical composition (hygroscopicity). We developed and applied models of aqueous phase SOA formation in cloud droplets and aerosol particles (aqSOA). Placing our model results into the context of laboratory, model and field studies suggests a potentially significant contribution of aqSOA to the global organic mass loading. The second focus of our work has been the analysis of ambient data of particles that might act as cloud condensation nuclei (CCN) at different locations and emission scenarios. Our model studies showed that the description of particle chemical composition and mixing state can often be greatly simplified, in particular in aged aerosol. While over the past years many CCN studies have been successful performed by using such simplified composition/mixing state assumptions, much more uncertainty exists in aerosol-cloud interactions in cold clouds (ice or mixed-phase). Therefore we extended our parcel model that describes warm cloud formation by ice microphysics and explored microphysical parameters that determine the phase state and lifetime of Arctic mixed-phase clouds.

  15. Modelled Black Carbon Radiative Forcing and Atmospheric Lifetime in AeroCom Phase II Constrained by Aircraft Observations

    SciTech Connect (OSTI)

    Samset, B. H.; Myhre, G.; Herber, Andreas; Kondo, Yutaka; Li, Shao-Meng; Moteki, N.; Koike, Makoto; Oshima, N.; Schwarz, Joshua P.; Balkanski, Y.; Bauer, S.; Bellouin, N.; Berntsen, T.; Bian, Huisheng; Chin, M.; Diehl, Thomas; Easter, Richard C.; Ghan, Steven J.; Iversen, T.; Kirkevag, A.; Lamarque, Jean-Francois; Lin, Guang; Liu, Xiaohong; Penner, Joyce E.; Schulz, M.; Seland, O.; Skeie, R. B.; Stier, P.; Takemura, T.; Tsigaridis, Kostas; Zhang, Kai

    2014-11-27

    Black carbon (BC) aerosols absorb solar radiation, and are generally held to exacerbate global warming through exerting a positive radiative forcing1. However, the total contribution of BC to the ongoing changes in global climate is presently under debate2-8. Both anthropogenic BC emissions and the resulting spatial and temporal distribution of BC concentration are highly uncertain2,9. In particular, long range transport and processes affecting BC atmospheric lifetime are poorly understood, leading to large estimated uncertainty in BC concentration at high altitudes and far from emission sources10. These uncertainties limit our ability to quantify both the historical, present and future anthropogenic climate impact of BC. Here we compare vertical profiles of BC concentration from four recent aircraft measurement campaigns with 13 state of the art aerosol models, and show that recent assessments may have overestimated present day BC radiative forcing. Further, an atmospheric lifetime of BC of less than 5 days is shown to be essential for reproducing observations in transport dominated remote regions. Adjusting model results to measurements in remote regions, and at high altitudes, leads to a 25% reduction in the multi-model median direct BC forcing from fossil fuel and biofuel burning over the industrial era.

  16. Alveolar targeting of aerosol pentamidine. Toward a rational delivery system

    SciTech Connect (OSTI)

    Simonds, A.K.; Newman, S.P.; Johnson, M.A.; Talaee, N.; Lee, C.A.; Clarke, S.W. )

    1990-04-01

    Nebulizer systems that deposit a high proportion of aerosolized pentamidine on large airways are likely to be associated with marked adverse side effects, which may lead to premature cessation of treatment. We have measured alveolar deposition and large airway-related side effects (e.g., cough, breathlessness, and effect on pulmonary function) after aerosolization of 150 mg pentamidine isethionate labeled with {sup 99m}Tc-Sn-colloid. Nine patients with AIDS were studied using three nebulizer systems producing different droplet size profiles: the Acorn System 22, Respirgard II, and Respirgard II with the inspiratory baffle removed. Alveolar deposition was greatest and side effects least with the nebulizer producing the smallest droplet size profile (Respirgard II), whereas large airway-related side effects were prominent and alveolar deposition lowest with the nebulizer producing the largest droplet size (Acorn System 22). Values for alveolar deposition and adverse airway effects were intermediate using the Respirgard with inspiratory baffle removed, thus indicating the importance of the baffle valve in determining droplet size. Addition of a similar baffle valve to the Acorn System 22 produced a marked improvement in droplet size profile. Selection of a nebulizer that produces an optimal droplet size range offers the advantage of enhancing alveolar targeting of aerosolized pentamidine while reducing large airway-related side effects.

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

    SciTech Connect (OSTI)

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

    2012-08-22

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

  18. Aerosol Observing System Upgraded

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity ofkandz-cm11 OutreachProductswsicloudwsiclouddenDVA N C E D B L O O D S TA I N P A T T E R N A NA LY S IDOE Office2 Aerosol

  19. A Temperature and Abundance Retrieval Method for Exoplanet Atmospheres

    E-Print Network [OSTI]

    Madhusudhan, Nikku

    We present a new method to retrieve molecular abundances and temperature profiles from exoplanet atmosphere photometry and spectroscopy. We run millions of one-dimensional (1D) atmosphere models in order to cover the large ...

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

    SciTech Connect (OSTI)

    Menon, Surabi; Del Genio, Anthony D.

    2007-09-03

    Any attempt to reconcile observed surface temperature changes within the last 150 years to changes simulated by climate models that include various atmospheric forcings is sensitive to the changes attributed to aerosols and aerosol-cloud-climate interactions, which are the main contributors that may well balance the positive forcings associated with greenhouse gases, absorbing aerosols, ozone related changes, etc. These aerosol effects on climate, from various modeling studies discussed in Menon (2004), range from +0.8 to -2.4 W m{sup -2}, with an implied value of -1.0 W m{sup -2} (range from -0.5 to -4.5 W m{sup -2}) for the aerosol indirect effects. Quantifying the contribution of aerosols and aerosol-cloud interactions remain complicated for several reasons some of which are related to aerosol distributions and some to the processes used to represent their effects on clouds. Aerosol effects on low lying marine stratocumulus clouds that cover much of the Earth's surface (about 70%) have been the focus of most of prior aerosol-cloud interaction effect simulations. Since cumulus clouds (shallow and deep convective) are short lived and cover about 15 to 20% of the Earth's surface, they are not usually considered as radiatively important. However, the large amount of latent heat released from convective towers, and corresponding changes in precipitation, especially in biomass regions due to convective heating effects (Graf et al. 2004), suggest that these cloud systems and aerosol effects on them, must be examined more closely. The radiative heating effects for mature deep convective systems can account for 10-30% of maximum latent heating effects and thus cannot be ignored (Jensen and Del Genio 2003). The first study that isolated the sensitivity of cumulus clouds to aerosols was from Nober et al. (2003) who found a reduction in precipitation in biomass burning regions and shifts in circulation patterns. Aerosol effects on convection have been included in other models as well (cf. Jacobson, 2002) but the relative impacts on convective and stratiform processes were not separated. Other changes to atmospheric stability and thermodynamical quantities due to aerosol absorption are also known to be important in modifying cloud macro/micro properties. Linkages between convection and boreal biomass burning can also impact the upper troposphere and lower stratosphere, radiation and cloud microphysical properties via transport of tropospheric aerosols to the lower stratosphere during extreme convection (Fromm and Servranckx 2003). Relevant questions regarding the impact of biomass aerosols on convective cloud properties include the effects of vertical transport of aerosols, spatial and temporal distribution of rainfall, vertical shift in latent heat release, phase shift of precipitation, circulation and their impacts on radiation. Over land surfaces, a decrease in surface shortwave radiation ({approx} 3-6 W m{sup -2} per decade) has been observed between 1960 to 1990, whereas, increases of 0.4 K in land temperature during the same period that occurred have resulted in speculations that evaporation and precipitation should also have decreased (Wild et al. 2004). However, precipitation records for the same period over land do not indicate any significant trend (Beck et al. 2005). The changes in precipitation are thought to be related to increased moisture advection from the oceans (Wild et al. 2004), which may well have some contributions from aerosol-radiation-convection coupling that could modify circulation patterns and hence moisture advection in specific regions. Other important aspects of aerosol effects, besides the direct, semi-direct, microphysical and thermodynamical impacts include alteration of surface albedos, especially snow and ice covered surfaces, due to absorbing aerosols. These effects are uncertain (Jacobson, 2004) but may produce as much as 0.3 W m{sup -2} forcing in the Northern hemisphere that could contribute to melting of ice and permafrost and change in the length of the season (e.g. early arrival of Spring

  1. The Model of Emissions of Gases and Aerosols from Nature version 2.1 (MEGAN2.1): an extended and updated framework for modeling biogenic emissions

    E-Print Network [OSTI]

    Guenther, A. B.

    The Model of Emissions of Gases and Aerosols from Nature version 2.1 (MEGAN2.1) is a modeling framework for estimating fluxes of biogenic compounds between terrestrial ecosystems and the atmosphere using simple mechanistic ...

  2. Aerosol plume transport and transformation in high spectral resolution lidar measurements and WRF-Flexpart simulations during the MILAGRO Field Campaign

    E-Print Network [OSTI]

    de Foy, B.

    The Mexico City Metropolitan Area (MCMA) experiences high loadings of atmospheric aerosols from anthropogenic sources, biomass burning and wind-blown dust. This paper uses a combination of measurements and numerical ...

  3. Atmospheric Neutrinos

    E-Print Network [OSTI]

    Thomas K. Gaisser

    2006-12-11

    This paper is a brief overview of the theory and experimental data of atmospheric neutrino production at the fiftieth anniversary of the experimental discovery of neutrinos.

  4. FY 2011 Second Quarter: Demonstration of New Aerosol Measurement Verification Testbed for Present-Day Global Aerosol Simulations

    SciTech Connect (OSTI)

    Koch, D

    2011-03-20

    The regional-scale Weather Research and Forecasting (WRF) model is being used by a DOE Earth System Modeling (ESM) project titled “Improving the Characterization of Clouds, Aerosols and the Cryosphere in Climate Models” to evaluate the performance of atmospheric process modules that treat aerosols and aerosol radiative forcing in the Arctic. We are using a regional-scale modeling framework for three reasons: (1) It is easier to produce a useful comparison to observations with a high resolution model; (2) We can compare the behavior of the CAM parameterization suite with some of the more complex and computationally expensive parameterizations used in WRF; (3) we can explore the behavior of this parameterization suite at high resolution. Climate models like the Community Atmosphere Model version 5 (CAM5) being used within the Community Earth System Model (CESM) will not likely be run at mesoscale spatial resolutions (10–20 km) until 5–10 years from now. The performance of the current suite of physics modules in CAM5 at such resolutions is not known, and current computing resources do not permit high-resolution global simulations to be performed routinely. We are taking advantage of two tools recently developed under PNNL Laboratory Directed Research and Development (LDRD) projects for this activity. The first is the Aerosol Modeling Testbed (Fast et al., 2011b), a new computational framework designed to streamline the process of testing and evaluating aerosol process modules over a range of spatial and temporal scales. The second is the CAM5 suite of physics parameterizations that have been ported into WRF so that their performance and scale dependency can be quantified at mesoscale spatial resolutions (Gustafson et al., 2010; with more publications in preparation).

  5. CARES Helps Explain Secondary Organic Aerosols

    ScienceCinema (OSTI)

    Zaveri, Rahul

    2014-06-02

    What happens when urban man-made pollution mixes with what we think of as pristine forest air? To know more about what this interaction means for the climate, the Carbonaceous Aerosol and Radiative Effects Study, or CARES, field campaign was designed in 2010. The sampling strategy during CARES was coordinated with CalNex 2010, another major field campaign that was planned in California in 2010 by the California Air Resources Board (CARB), the National Oceanic and Atmospheric Administration (NOAA), and the California Energy Commission (CEC). "We found two things. When urban pollution mixes with forest pollutions we get more secondary organic aerosols," said Rahul Zaveri, FCSD scientist and project lead on CARES. "SOAs are thought to be formed primarily from forest emissions but only when they interact with urban emissions. The data is saying that there will be climate cooling over the central California valley because of these interactions." Knowledge gained from detailed analyses of data gathered during the CARES campaign, together with laboratory experiments, is being used to improve existing climate models.

  6. CARES Helps Explain Secondary Organic Aerosols

    SciTech Connect (OSTI)

    Zaveri, Rahul

    2014-03-28

    What happens when urban man-made pollution mixes with what we think of as pristine forest air? To know more about what this interaction means for the climate, the Carbonaceous Aerosol and Radiative Effects Study, or CARES, field campaign was designed in 2010. The sampling strategy during CARES was coordinated with CalNex 2010, another major field campaign that was planned in California in 2010 by the California Air Resources Board (CARB), the National Oceanic and Atmospheric Administration (NOAA), and the California Energy Commission (CEC). "We found two things. When urban pollution mixes with forest pollutions we get more secondary organic aerosols," said Rahul Zaveri, FCSD scientist and project lead on CARES. "SOAs are thought to be formed primarily from forest emissions but only when they interact with urban emissions. The data is saying that there will be climate cooling over the central California valley because of these interactions." Knowledge gained from detailed analyses of data gathered during the CARES campaign, together with laboratory experiments, is being used to improve existing climate models.

  7. 2010 Atmospheric System Research (ASR) Science Team Meeting Summary

    SciTech Connect (OSTI)

    Dupont, DL

    2011-05-04

    This document contains the summaries of papers presented in poster format at the March 2010 Atmospheric System Research Science Team Meeting held in Bethesda, Maryland. More than 260 posters were presented during the Science Team Meeting. Posters were sorted into the following subject areas: aerosol-cloud-radiation interactions, aerosol properties, atmospheric state and surface, cloud properties, field campaigns, infrastructure and outreach, instruments, modeling, and radiation. To put these posters in context, the status of ASR at the time of the meeting is provided here.

  8. DEVELOPMENT OF FINE PARTICULATE EMISSION FACTORS AND SPECIATION PROFILES FOR OIL AND GAS-FIRED COMBUSTION SYSTEMS

    SciTech Connect (OSTI)

    Glenn C. England

    2004-10-20

    In 1997, the United States Environmental Protection Agency (EPA) promulgated new National Ambient Air Quality Standards (NAAQS) for particulate matter, including for the first time particles with aerodynamic diameter smaller than 2.5 micrometers ({micro}m) referred to as PM2.5. PM2.5 in the atmosphere also contributes to reduced atmospheric visibility, which is the subject of existing rules for siting emission sources near Class 1 areas and new Regional Haze rules. There are few existing data regarding emissions and characteristics of fine aerosols from oil, gas and power generation industry combustion sources, and the information that is available is generally outdated and incomplete. Traditional stationary source air emission sampling methods tend to underestimate or overestimate the contribution of the source to ambient aerosols because they do not properly account for primary aerosol formation, which occurs after the gases leave the stack. Primary aerosol includes both filterable particles that are solid or liquid aerosols at stack temperature plus those that form as the stack gases cool through mixing and dilution processes in the plume downwind of the source. These deficiencies in the current methods can have significant impacts on regulatory decision-making. PM2.5 measurement issues were extensively reviewed by the American Petroleum Institute (API) (England et al., 1998), and it was concluded that dilution sampling techniques are more appropriate for obtaining a representative particulate matter sample from combustion systems for determining PM2.5 emission rate and chemical speciation. Dilution sampling is intended to collect aerosols including those that condense and/or react to form solid or liquid aerosols as the exhaust plume mixes and cools to near-ambient temperature immediately after the stack discharge. These techniques have been widely used in recent research studies. For example, Hildemann et al. (1994) and McDonald et al. (1998) used filtered ambient air to dilute the stack gas sample followed by 80-90 seconds residence time to allow aerosol formation and growth to stabilize prior to sample collection and analysis. More accurate and complete emissions data generated using the methods developed in this program will enable more accurate source-receptor and source apportionment analysis for PM2.5 National Ambient Air Quality Standards (NAAQS) implementation and streamline the environmental assessment of oil, gas and power production facilities. The overall goals of this program were to: (1) Develop improved dilution sampling technology and test methods for PM2.5 mass emissions and speciation measurements, and compare results obtained with dilution and traditional stationary source sampling methods. (2) Develop emission factors and speciation profiles for emissions of fine particulate matter, especially organic aerosols, for use in source-receptor and source apportionment analyses. (3) Identify and characterize PM2.5 precursor compound emissions that can be used in source-receptor and source apportionment analyses.

  9. AERONET: The Aerosol Robotic Network

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    AERONET collaboration provides globally distributed observations of spectral aerosol optical Depth (AOD), inversion products, and precipitable water in diverse aerosol regimes. Aerosol optical depth data are computed for three data quality levels: Level 1.0 (unscreened), Level 1.5 (cloud-screened), and Level 2.0 (cloud screened and quality-assured). Inversions, precipitable water, and other AOD-dependent products are derived from these levels and may implement additional quality checks.[Copied from http://aeronet.gsfc.nasa.gov/new_web/system_descriptions.html

  10. eDPS Aerosol Collection

    SciTech Connect (OSTI)

    Venzie, J.

    2015-10-13

    The eDPS Aerosol Collection project studies the fundamental physics of electrostatic aerosol collection for national security applications. The interpretation of aerosol data requires understanding and correcting for biases introduced from particle genesis through collection and analysis. The research and development undertaken in this project provides the basis for both the statistical correction of existing equipment and techniques; as well as, the development of new collectors and analytical techniques designed to minimize unwanted biases while improving the efficiency of locating and measuring individual particles of interest.

  11. Assessing regional scale predictions of aerosols, marine stratocumulus, and their interactions during VOCALS-REx using WRF-Chem

    SciTech Connect (OSTI)

    Yang Q.; Lee Y.; Gustafson Jr., W. I.; Fast, J. D.; Wang, H.; Easter, R. C.; Morrison, H.; Chapman, E. G.; Spak, S. N.; Mena-Carrasco, M. A.

    2011-12-02

    This study assesses the ability of the recent chemistry version (v3.3) of the Weather Research and Forecasting (WRF-Chem) model to simulate boundary layer structure, aerosols, stratocumulus clouds, and energy fluxes over the Southeast Pacific Ocean. Measurements from the VAMOS Ocean-Cloud-Atmosphere-Land Study Regional Experiment (VOCALS-REx) and satellite retrievals (i.e., products from the MODerate resolution Imaging Spectroradiometer (MODIS), Clouds and Earth's Radiant Energy System (CERES), and GOES-10) are used for this assessment. The Morrison double-moment microphysics scheme is newly coupled with interactive aerosols in the model. The 31-day (15 October-16 November 2008) WRF-Chem simulation with aerosol-cloud interactions (AERO hereafter) is also compared to a simulation (MET hereafter) with fixed cloud droplet number concentrations in the microphysics scheme and simplified cloud and aerosol treatments in the radiation scheme. The well-simulated aerosol quantities (aerosol number, mass composition and optical properties), and the inclusion of full aerosol-cloud couplings lead to significant improvements in many features of the simulated stratocumulus clouds: cloud optical properties and microphysical properties such as cloud top effective radius, cloud water path, and cloud optical thickness. In addition to accounting for the aerosol direct and semi-direct effects, these improvements feed back to the simulation of boundary-layer characteristics and energy budgets. Particularly, inclusion of interactive aerosols in AERO strengthens the temperature and humidity gradients within the capping inversion layer and lowers the marine boundary layer (MBL) depth by 130 m from that of the MET simulation. These differences are associated with weaker entrainment and stronger mean subsidence at the top of the MBL in AERO. Mean top-of-atmosphere outgoing shortwave fluxes, surface latent heat, and surface downwelling longwave fluxes are in better agreement with observations in AERO, compared to the MET simulation. Nevertheless, biases in some of the simulated meteorological quantities (e.g., MBL temperature and humidity) and aerosol quantities (e.g., underestimations of accumulation mode aerosol number) might affect simulated stratocumulus and energy fluxes over the Southeastern Pacific, and require further investigation. The well-simulated timing and outflow patterns of polluted and clean episodes demonstrate the model's ability to capture daily/synoptic scale variations of aerosol and cloud properties, and suggest that the model is suitable for studying atmospheric processes associated with pollution outflow over the ocean. The overall performance of the regional model in simulating mesoscale clouds and boundary layer properties is encouraging and suggests that reproducing gradients of aerosol and cloud droplet concentrations and coupling cloud-aerosol-radiation processes are important when simulating marine stratocumulus over the Southeast Pacific.

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

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Meskhidze, Nicholas; Nenes, Athanasios

    2010-01-01

    Using satellite 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 previousmore »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

  13. Aerosol penetration through transport lines 

    E-Print Network [OSTI]

    Dileep, V.R.

    1996-01-01

    It is very important to minimize the losses in aerosol transport systems for the Continuous Air Monitors (CAM) to have a prompt and a meaningful alarm and the U.S. Environmental Protection Agency (EPA) also Currently mandates continuous emissions...

  14. Aerosol characterization study using multi-spectrum remote sensing measurement techniques.

    SciTech Connect (OSTI)

    Glen, Crystal Chanea; Sanchez, Andres L.; Lucero, Gabriel Anthony; Schmitt, Randal L.; Johnson, Mark S.; Tezak, Matthew Stephen; Servantes, Brandon Lee

    2013-09-01

    A unique aerosol flow chamber coupled with a bistatic LIDAR system was implemented to measure the optical scattering cross sections and depolarization ratio of common atmospheric particulates. Each of seven particle types (ammonium sulfate, ammonium nitrate, sodium chloride, potassium chloride, black carbon and Arizona road dust) was aged by three anthropogenically relevant mechanisms: 1. Sulfuric acid deposition, 2. Toluene ozonolysis reactions, and 3. m-Xylene ozonolysis reactions. The results of pure particle scattering properties were compared with their aged equivalents. Results show that as most particles age under industrial plume conditions, their scattering cross sections are similar to pure black carbon, which has significant impacts to our understanding of aerosol impacts on climate. In addition, evidence emerges that suggest chloride-containing aerosols are chemically altered during the organic aging process. Here we present the direct measured scattering cross section and depolarization ratios for pure and aged atmospheric particulates.

  15. White Paper: Airborne Observations in Western North Dakota to Obtain Baseline Measurements for Qualification of Important Atmospheric Components

    E-Print Network [OSTI]

    Delene, David J.

    and aerosols. The production, transportation and storage of crude oil and natural gas can result in methane atoms) vapors from crude oil production form aerosols within the atmosphere. The research objective determine the magnitude of emission rates from the region's oil and gas production (Karion et al. 2013

  16. Formation mechanisms and quantification of organic nitrates in atmospheric aerosol

    E-Print Network [OSTI]

    Rollins, Andrew Waite

    2010-01-01

    limonene-1-nitrate, 1-hydroxy-butane- 2-nitrate, 3-hydroxy-our measured spectra of the butane hydroxynitrate we foundstandards except for the butane hydroxynitrate the O/C based

  17. Formation mechanisms and quantification of organic nitrates in atmospheric aerosol

    E-Print Network [OSTI]

    Rollins, Andrew Waite

    2010-01-01

    the nitrate radical (no 3 ) with isoprene, 1,3-butadiene and2,3-dimethyl- 1,3-butadiene in air, Atmos. Environ. , 26A(Isoprene (2-methyl-1,3-butadiene) is globally the most

  18. Atmospheric aerosol optical property retrieval with scanning polarimeters

    E-Print Network [OSTI]

    scatter and absorb incident solar radiation and emitted infra-red radiation. Climate models simulate Mexico suspended over low altitude marine stratocumulus clouds in the Gulf of Mexico. These studies

  19. AIRBORNE HIGH SPECTRAL RESOLUTION LIDAR MEASUREMENTS OF ATMOSPHERIC AEROSOLS

    E-Print Network [OSTI]

    the evolution and transport of pollution from Mexico City. The second major experiment was the Texas Air Quality, A., University of Hawaii, Department of Oceanography University of Hawaii, Honolulu, HI 96822 Air B200 aircraft during several field experiments. Most of the flights were conducted during two

  20. Nonequilibrium atmospheric secondary organic aerosol formation and growth

    E-Print Network [OSTI]

    2012-01-01

    mass spectrometry (SPLAT-II) show that the SOA containsfrom NO ţ and NO 2 ţ (SPLAT-II spectra show primarily m?zand the densities mea- sured by SPLAT-II, the total mass

  1. ATMOSPHERIC AEROSOL RESEARCH ANNUAL REPORT 1975-76

    E-Print Network [OSTI]

    Novakov, T.

    2010-01-01

    particles from propane-benzene combustion in air; b) exhaustsoot particles from propane-benzene combustion in air; (b)particles produced by combustion of propane saturated with

  2. ATMOSPHERIC AEROSOL RESEARCH ANNUAL REPORT 1975-76

    E-Print Network [OSTI]

    Novakov, T.

    2010-01-01

    propane-benzene combustion in air; b) exhaust particles from an internal combustion engine;propane-benzene combustion in air; (b) exhaust particulates from an internal combustion engine; (

  3. Atmospheric Science Program Cumulus Humilis Aerosol Processing Study (CHAPS)

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity ofkandz-cm11 OutreachProductswsicloudwsiclouddenDVA N C E D B L O O DBiomass and BiofuelsPhysicist47July 1999Science Program

  4. The Atmosphere as a Laboratory: Aerosols, Air Quality, and Climate |

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity ofkandz-cm11 Outreach Home RoomPreservationBio-Inspired Solar FuelTechnologyTel: Name: Rm. Tel:Test1The Ames ProjectPrinceton

  5. Impacts of greenhouse gases and aerosol direct and indirect effects on clouds and

    E-Print Network [OSTI]

    Dufresne, Jean-Louis

    Impacts of greenhouse gases and aerosol direct and indirect effects on clouds and radiation/C.N.R.S., Villeneuve d'Ascq, France Among anthropogenic perturbations of the Earth's atmosphere, greenhouse gases the radiative impacts of five species of greenhouse gases (CO2, CH4, N2O, CFC-11 and CFC-12) and sulfate

  6. Aerosol Optical Depth Retrieval by Neural Networks Ensemble with Adaptive Cost Function

    E-Print Network [OSTI]

    Obradovic, Zoran

    and warming the atmosphere. Therefore, the accurate prediction of aerosols composition and their concentration (AERONET) is global remote sensing network of about 540 ground-based radiometers that retrieve AOD several as ground truth when validating retrieval quality of various satellite- based AOD retrieval algorithms [4

  7. DIESEL AEROSOL SAMPLING IN THE David Kittelson, Jason Johnson, and Winthrop Watts

    E-Print Network [OSTI]

    Minnesota, University of

    chemical composition of diesel particulate matter collected in laboratory and in wind tunnel #12;In OrderDIESEL AEROSOL SAMPLING IN THE ATMOSPHERE David Kittelson, Jason Johnson, and Winthrop Watts Center for Diesel Research University of Minnesota 10th CRC ON-ROAD VEHICLE EMISSIONS WORKSHOP San Diego, California

  8. FOSSIL ENERGY, CO2, CLIMATE CHANGE, AND THE AEROSOL PROBLEM Stephen E. Schwartz

    E-Print Network [OSTI]

    (energy penalty). Consequently, until alternative energy sources are developed or a practical meansFOSSIL ENERGY, CO2, CLIMATE CHANGE, AND THE AEROSOL PROBLEM Stephen E. Schwartz For presentation of Energy Office of Science ABSTRACT Climate change due to increasing atmospheric carbon dioxide differs

  9. Global observations and spectral characteristics of desert dust and biomass burning aerosols

    E-Print Network [OSTI]

    Graaf, Martin de

    the advantage of monitoring of the global atmosphere. The disadvantage is often a poor spacial reso- lution quantity, but a radiation difference in the UV. Its main advantages are its insensitivity to scattering in climate physics today is the effect of aerosols on the global energy budget. The amount and sign

  10. Aerosol properties and their influences on marine boundary layer cloud condensation nuclei

    E-Print Network [OSTI]

    Dong, Xiquan

    and early spring months had the highest mean surface wind speed (> 5 m sŔ1 ) and greatest contribution of aerosols found in the atmosphere such as mineral dust, urban/industrial pollution, biomass burning, and sea by using observations and model simulations [Rosenfeld et al., 2008; Li et al., 2011; Feingold et al., 2006

  11. Niamey Aerosol Optical Depths

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Flynn, Connor

    2008-10-01

    MFRSR irradiance data collected during the ACRF AMF deployment in Niamey, Niger have been used to derive AOD for five wavelength channels of the MFRSR. These data have been corrected to adjust for filter drift over the course of the campaign and contamination due to forward scattering as a result of large dust particles in the atmosphere around Niamey.

  12. Nanomaterials from Aerosols Aerosols are suspensions of liquid or solid particles in a gas. Aerosol particles

    E-Print Network [OSTI]

    Beaucage, Gregory

    changes which are evidenced by changes in the temperature of the oceans and rapid melting of the polar and glacial ice packs. Of pollution sources, aerosols represent the least understood and could potentially

  13. Chemical and Physical Characteristics of Diesel Aerosol | Department...

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    and Physical Characteristics of Diesel Aerosol Chemical and Physical Characteristics of Diesel Aerosol 2002 DEER Conference Presentation: University of Minnesota...

  14. Atmospheric Radiation Measurement Climate Research Facility (ACRF) Annual Report 2007

    SciTech Connect (OSTI)

    LR Roeder

    2007-12-01

    This annual report describes the purpose and structure of the program, and presents key accomplishments in 2007. Notable achievements include: • Successful review of the ACRF as a user facility by the DOE Biological and Environmental Research Advisory Committee. The subcommittee reinforced the importance of the scientific impacts of this facility, and its value for the international research community. • Leadership of the Cloud Land Surface Interaction Campaign. This multi-agency, interdisciplinary field campaign involved enhanced surface instrumentation at the ACRF Southern Great Plains site and, in concert with the Cumulus Humilis Aerosol Processing Study sponsored by the DOE Atmospheric Science Program, coordination of nine aircraft through the ARM Aerial Vehicles Program. • Successful deployment of the ARM Mobile Facility in Germany, including hosting nearly a dozen guest instruments and drawing almost 5000 visitors to the site. • Key advancements in the representation of radiative transfer in weather forecast models from the European Centre for Medium-Range Weather Forecasts. • Development of several new enhanced data sets, ranging from best estimate surface radiation measurements from multiple sensors at all ACRF sites to the extension of time-height cloud occurrence profiles to Niamey, Niger, Africa. • Publication of three research papers in a single issue (February 2007) of the Bulletin of the American Meteorological Society.

  15. Determination of vertical profiles of aerosol extinction, single scatter

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration would like submit theCovalent BondingMeeting |Design CompetitionsFuelofSourcesalbedo and

  16. Global distribution and climate forcing of marine organic aerosol: 1. Model improvements and evaluation

    SciTech Connect (OSTI)

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

    2011-11-23

    Marine organic aerosol emissions have been implemented and evaluated within the National Center of Atmospheric Research (NCAR)'s Community Atmosphere Model (CAM5) with the Pacific Northwest National Laboratory's 7-mode Modal Aerosol Module (MAM-7). Emissions of marine primary organic aerosols (POA), phytoplanktonproduced isoprene- and monoterpenes-derived secondary organic aerosols (SOA) and methane sulfonate (MS{sup -}) are shown to affect surface concentrations of organic aerosols in remote marine regions. Global emissions of submicron marine POA is estimated to be 7.9 and 9.4 Tg yr{sup -1}, for the Gantt et al. (2011) and Vignati et al. (2010) emission parameterizations, respectively. Marine sources of SOA and particulate MS{sup -} (containing both sulfur and carbon atoms) contribute an additional 0.2 and 5.1 Tg yr{sup -1}, respectively. Widespread areas over productive waters of the Northern Atlantic, Northern Pacific, and the Southern Ocean show marine-source submicron organic aerosol surface concentrations of 100 ngm{sup -3}, with values up to 400 ngm{sup -3} over biologically productive areas. Comparison of long-term surface observations of water insoluble organic matter (WIOM) with POA concentrations from the two emission parameterizations shows that despite revealed discrepancies (often more than a factor of 2), both Gantt et al. (2011) and Vignati et al. (2010) formulations are able to capture the magnitude of marine organic aerosol concentrations, with the Gantt et al. (2011) parameterization attaining better seasonality. Model simulations show that the mixing state of the marine POA can impact the surface number concentration of cloud condensation nuclei (CCN). The largest increases (up to 20 %) in CCN (at a supersaturation (S) of 0.2 %) number concentration are obtained over biologically productive ocean waters when marine organic aerosol is assumed to be externally mixed with sea-salt. Assuming marine organics are internally-mixed with sea-salt provides diverse results with increases and decreases in the concentration of CCN over different parts of the ocean. The sign of the CCN change due to the addition of marine organics to seasalt aerosol is determined by the relative significance of the increase in mean modal diameter due to addition of mass, and the decrease in particle hygroscopicity due to compositional changes in marine aerosol. Based on emerging evidence for increased CCN concentration over biologically active surface ocean areas/periods, our study suggests that treatment of sea spray in global climate models (GCMs) as an internal mixture of marine organic aerosols and sea-salt will likely lead to an underestimation in CCN number concentration.

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

    SciTech Connect (OSTI)

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

    2012-07-25

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

  18. European Atmospheric Pollution Imported by Cooler Air Masses to

    E-Print Network [OSTI]

    Einat, Aharonov

    European Atmospheric Pollution Imported by Cooler Air Masses to the Eastern Mediterranean during between PT modes and air pollution episodes over the East Mediterranean (5-9) led us to adopt the same months aerosols collected in Israel are highly polluted by metals (EFNi ) 120, EFCu ) 320, EFZn ) 30

  19. Atmospheric Radiation Measurement Climate Research Facility (ACRF) Annual Report 2008

    SciTech Connect (OSTI)

    LR Roeder

    2008-12-01

    The Importance of Clouds and Radiation for Climate Change: The Earth’s surface temperature is determined by the balance between incoming solar radiation and thermal (or infrared) radiation emitted by the Earth back to space. Changes in atmospheric composition, including greenhouse gases, clouds, and aerosols, can alter this balance and produce significant climate change. Global climate models (GCMs) are the primary tool for quantifying future climate change; however, there remain significant uncertainties in the GCM treatment of clouds, aerosol, and their effects on the Earth’s energy balance. In 1989, the U.S. Department of Energy (DOE) Office of Science created the Atmospheric Radiation Measurement (ARM) Program to address scientific uncertainties related to global climate change, with a specific focus on the crucial role of clouds and their influence on the transfer of radiation in the atmosphere. To reduce these scientific uncertainties, the ARM Program uses a unique twopronged approach: • The ARM Climate Research Facility, a scientific user facility for obtaining long-term measurements of radiative fluxes, cloud and aerosol properties, and related atmospheric characteristics in diverse climate regimes; and • The ARM Science Program, focused on the analysis of ACRF and other data to address climate science issues associated with clouds, aerosols, and radiation, and to improve GCMs. This report provides an overview of each of these components and a sample of achievements for each in fiscal year (FY) 2008.

  20. Cheng-Hsuan Lu Atmospheric Sciences and Research Center

    E-Print Network [OSTI]

    Alexandrova, Ivana

    and aerosols in Goddard Earth Observing System Model, Version 5 (GEOS-5) by introducing a double-moment cloud component of the Community Earth System Model (CESM) primarily at the National Center for Atmospheric global models (i.e., the Global Forecast System, GFS, and the Climate Forecast System, CFS). Our proposed

  1. Effects of Aerosols on Autumn Precipitation over Mid-Eastern China

    SciTech Connect (OSTI)

    Chen, Siyu; Huang, J.; Qian, Yun; Ge, Jinming; Su, Jing

    2014-09-20

    Long-term observational data indicated a decreasing trend for the amount of autumn precipitation (i.e. 54.3 mm per decade) over Mid-Eastern China, especially after 1980s (~ 5.6% per decade). To examine the cause of the decreasing trend, the mechanisms associated with the change of autumn precipitation were investigated from the perspective of water vapor transportation, atmospheric stability and cloud microphysics. Results show that the decrease of convective available potential energy (i.e. 12.81 J kg-1/ decade) and change of cloud microphysics, which were closely related to the increase of aerosol loading during the past twenty years, were the two primary factors responsible for the decrease of autumn precipitation. Ours results showed that increased aerosol could enhance the atmospheric stability thus weaken the convection. Meanwhile, more aerosols also led to a significant decline of raindrop concentration and to a delay of raindrop formation because of smaller size of cloud droplets. Thus, increased aerosols produced by air pollution could be one of the major reasons for the decrease of autumn precipitation. Furthermore, we found that the aerosol effects on precipitation in autumn was more significant than in other seasons, partly due to the relatively more stable synoptic system in autumn. The impact of large-scale circulation dominated in autumn and the dynamic influence on precipitation was more important than the thermodynamic activity.

  2. ARM - Field Campaign - In-situ Aerosol Profiles (Cessna Aerosol Flights)

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity ofkandz-cm11 Comments? WeDatastreamstps DocumentationAtlanticENA ContactsProductsSACR26,

  3. THE INFLUENCE OF BENZENE AS A TRACE REACTANT IN TITAN AEROSOL ANALOGS

    SciTech Connect (OSTI)

    Trainer, Melissa G.; Sebree, Joshua A.; Heidi Yoon, Y.; Tolbert, Margaret A.

    2013-03-20

    Benzene has been detected in Titan's atmosphere by Cassini instruments, with concentrations ranging from sub-ppb in the stratosphere to ppm in the ionosphere. Sustained levels of benzene in the haze formation region could signify that it is an important reactant in the formation of Titan's organic aerosol. To date, there have not been laboratory investigations to assess the influence of benzene on aerosol properties. We report a laboratory study on the chemical composition of organic aerosol formed from C{sub 6}H{sub 6}/CH{sub 4}/N{sub 2} via far ultraviolet irradiation (120-200 nm). The compositional results are compared to those from aerosol generated by a more ''traditional Titan'' mixture of CH{sub 4}/N{sub 2}. Our results show that even a trace amount of C{sub 6}H{sub 6} (10 ppm) has significant impact on the chemical composition and production rates of organic aerosol. There are several pathways by which photolyzed benzene may react to form larger molecules, both with and without the presence of CH{sub 4}, but many of these reaction mechanisms are only beginning to be explored for the conditions at Titan. Continued work investigating the influence of benzene in aerosol growth will advance understanding of this previously unstudied reaction system.

  4. 4, 20552088, 2004 Aerosol-ozone

    E-Print Network [OSTI]

    Boyer, Edmond

    ACPD 4, 2055­2088, 2004 Aerosol-ozone correlations during dust transport episodes P. Bonasoni et al and Physics Discussions Aerosol-ozone correlations during dust transport episodes P. Bonasoni1 , P.bonasoni@isac.cnr.it) 2055 #12;ACPD 4, 2055­2088, 2004 Aerosol-ozone correlations during dust transport episodes P. Bonasoni

  5. Real time infrared aerosol analyzer

    DOE Patents [OSTI]

    Johnson, Stanley A. (Countryside, IL); Reedy, Gerald T. (Bourbonnais, IL); Kumar, Romesh (Naperville, IL)

    1990-01-01

    Apparatus for analyzing aerosols in essentially real time includes a virtual impactor which separates coarse particles from fine and ultrafine particles in an aerosol sample. The coarse and ultrafine particles are captured in PTFE filters, and the fine particles impact onto an internal light reflection element. The composition and quantity of the particles on the PTFE filter and on the internal reflection element are measured by alternately passing infrared light through the filter and the internal light reflection element, and analyzing the light through infrared spectrophotometry to identify the particles in the sample.

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

    SciTech Connect (OSTI)

    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).

  7. Sources and composition of submicron organic mass in marine aerosol particles: Marine Aerosol Organic Mass Composition

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Frossard, Amanda A.; Russell, Lynn M.; Burrows, Susannah M.; Elliott, Scott M.; Bates, Timothy S.; Quinn, Patricia K.

    2014-11-26

    Recent studies have proposed a variety of interpretations of the sources and composition of atmospheric marine aerosol particles (aMA) based on a range of physical and chemical measurements collected during open-ocean research cruises. To investigate the processes that affect marine organic particles, this study uses the characteristic functional group composition (from Fourier transform infrared (FTIR) spectroscopy) of aMAP from five ocean regions to show that: (i) The organic functional group composition of aMAP that can be identified as atmospheric primary marine (ocean-derived) aerosol (aPMA) is 65±12% hydroxyl, 21±9% alkane, 6±6% amine, and 7±8% carboxylic acid functional groups. Contributions from photochemicalmore »reactions add carboxylic acid groups (15%-25%), shipping effluent in seawater and ship emissions add additional alkane groups (up to 70%), and coastal emissions mix in alkane and carboxylic acid groups from coastal pollution sources. (ii) The organic composition of aPMA is nearly identical to model generated primary marine aerosol particles (gPMA) from bubbled seawater (55% hydroxyl, 32% alkane, and 13% amine functional groups), indicating that its overall functional group composition is the direct consequence of the organic constituents of the seawater source. (iii) While the seawater organic functional group composition was nearly invariant across all three ocean regions studied, the gPMA alkane group fraction increased with chlorophyll-a concentrations (r = 0.79). gPMA from productive seawater had a larger fraction of alkane functional groups (35%) compared to gPMA from non-productive seawater (16%), likely due to the presence of surfactants in productive seawater that stabilize the bubble film and lead to preferential drainage of the more soluble (lower alkane group fraction) organic components. gPMA has a hydroxyl group absorption peak location characteristic of monosaccharides and disaccharides, where the seawater OM hydroxyl group peak location is closer to that of polysaccharides. This may result from the larger saccharides preferentially remaining in the seawater during gPMA and aPMA production« less

  8. Sources and composition of submicron organic mass in marine aerosol particles: Marine Aerosol Organic Mass Composition

    SciTech Connect (OSTI)

    Frossard, Amanda A. [Univ. of California, San Diego, CA (United States). Scripps Inst. of Oceanography; Russell, Lynn M. [Univ. of California, San Diego, CA (United States). Scripps Inst. of Oceanography; Burrows, Susannah M. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States). Atmospheric Science and Global Change Div. (ASGC); Elliott, Scott M. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Bates, Timothy S. [National Oceanic and Atmospheric Administration (NOAA), Seattle, WA (United States). Pacific Marine Environmental Lab. (PMEL); Quinn, Patricia K. [National Oceanic and Atmospheric Administration (NOAA), Seattle, WA (United States). Pacific Marine Environmental Lab. (PMEL)

    2014-11-26

    Recent studies have proposed a variety of interpretations of the sources and composition of atmospheric marine aerosol particles (aMA) based on a range of physical and chemical measurements collected during open-ocean research cruises. To investigate the processes that affect marine organic particles, this study uses the characteristic functional group composition (from Fourier transform infrared (FTIR) spectroscopy) of aMAP from five ocean regions to show that: (i) The organic functional group composition of aMAP that can be identified as atmospheric primary marine (ocean-derived) aerosol (aPMA) is 65±12% hydroxyl, 21±9% alkane, 6±6% amine, and 7±8% carboxylic acid functional groups. Contributions from photochemical reactions add carboxylic acid groups (15%-25%), shipping effluent in seawater and ship emissions add additional alkane groups (up to 70%), and coastal emissions mix in alkane and carboxylic acid groups from coastal pollution sources. (ii) The organic composition of aPMA is nearly identical to model generated primary marine aerosol particles (gPMA) from bubbled seawater (55% hydroxyl, 32% alkane, and 13% amine functional groups), indicating that its overall functional group composition is the direct consequence of the organic constituents of the seawater source. (iii) While the seawater organic functional group composition was nearly invariant across all three ocean regions studied, the gPMA alkane group fraction increased with chlorophyll-a concentrations (r = 0.79). gPMA from productive seawater had a larger fraction of alkane functional groups (35%) compared to gPMA from non-productive seawater (16%), likely due to the presence of surfactants in productive seawater that stabilize the bubble film and lead to preferential drainage of the more soluble (lower alkane group fraction) organic components. gPMA has a hydroxyl group absorption peak location characteristic of monosaccharides and disaccharides, where the seawater OM hydroxyl group peak location is closer to that of polysaccharides. This may result from the larger saccharides preferentially remaining in the seawater during gPMA and aPMA production

  9. 6. Impact of smoke and moisture on shortwave radia7ve hea7ng profile Dynamical and Radia7ve Influences of Smoke Transport on the Southeast Atlan7c Atmospheric Ver7cal Structure

    E-Print Network [OSTI]

    Zuidema, Paquita

    6. Impact of smoke and moisture on shortwave radia7ve hea7ng profile-tropospheric air above the cloud-top inversion layer, thereby inhibi:ng the entrainment stability impac:ng the stratocumulus deck. What is the role of regional circula

  10. Stratospheric Albedo Modification by Aerosol Injection

    E-Print Network [OSTI]

    Katz, J I

    2009-01-01

    This paper reviews and develops the proposal, widely discussed but not examined in detail, to use stratospheric aerosols to increase the Earth's albedo to Solar radiation in order to control climate change. The potential of this method has been demonstrated by the "natural experiments" of volcanic injection of sulfate aerosols into the stratosphere that led to subsequent observed global cooling. I consider several hygroscopic oxides as possible aerosol materials in addition to oxides of sulfur. Aerosol chemistry, dispersion and transport have been the subject of little study and are not understood, representing a significant scientific risk. Even the optimal altitude of injection and aerosol size distribution are poorly known. Past attention focused on guns and airplanes as means of lofting aerosols or their chemical precursors, but large sounding rockets are cheap, energetically efficient, can be designed to inject aerosols at any required altitude, and involve little technical risk. Sophisticated, mass-opti...

  11. Stratospheric Aerosol Geoengineering ALAN ROBOCK

    E-Print Network [OSTI]

    Robock, Alan

    hydrologic responses, whitening of the skies, reduction of solar power, and impacts of diffuse radiation Project, conducting climate model experiments with standard stratospheric aerosol in- jection scenarios, which stated that ``It is extremely likely that human in- fluence has been the dominant cause

  12. Reactive processing of formaldehyde and acetaldehyde in aqueous aerosol mimics: Surface tension depression and secondary organic products

    E-Print Network [OSTI]

    Li, Zhi; Sareen, Neha; McNeill, V Faye

    2011-01-01

    The reactive uptake of carbonyl-containing volatile organic compounds (cVOCs) by aqueous atmospheric aerosols is a likely source of particulate organic material. The aqueous-phase secondary organic products of some cVOCs are surface-active. Therefore, cVOC uptake can lead to organic film formation at the gas-aerosol interface and changes in aerosol surface tension. We examined the chemical reactions of two abundant cVOCs, formaldehyde and acetaldehyde, in water and aqueous ammonium sulfate (AS) solutions mimicking tropospheric aerosols. Secondary organic products were identified using Aerosol Chemical Ionization Mass Spectrometry (Aerosol-CIMS), and changes in surface tension were monitored using pendant drop tensiometry. Hemiacetal oligomers and aldol condensation products were identified using Aerosol-CIMS. A hemiacetal sulfate ester was tentatively identified in the formaldehyde-AS system. Acetaldehyde depresses surface tension to 65(\\pm2) dyn/cm in pure water and 62(\\pm1) dyn/cm in AS solutions. Surface t...

  13. DO AEROSOLS CHANGE CLOUD COVER AND AFFECT CLIMATE?

    E-Print Network [OSTI]

    Schwartz, Stephen E.

    IN MEXICO CITY BASIN Light scattering by aerosols decreases absorption of solar radiation. #12;AEROSOLS;AEROSOL INFLUENCES ON CLIMATE AND CLIMATE CHANGE #12;DMS #12;AEROSOL IN MEXICO CITY BASIN #12;AEROSOL AS SEEN FROM SPACE Fire plumes from southern Mexico transported north into Gulf of Mexico. #12;CLOUD

  14. Identification of source contributions to visibility-reducing organic aerosols in the vicinity of Grand Canyon National Park. Interim final report

    SciTech Connect (OSTI)

    Mazurek, M.A.; Hallock, K.A.; Leach, M. [Brookhaven National Lab., Upton, NY (United States); Mason-Jones, M.; Mason-Jones, H.; Salmon, L.G.; Winner, D.A.; Cass, G.R. [California Inst. of Tech., Pasadena, CA (United States). Dept. of Environmental Engineering Science

    1993-06-01

    Sulfates and carbonaceous aerosols are the largest contributors to the fine particle burden in the atmosphere near Grand Canyon National Park. While the effects of sulfate particles on visibility at the Grand Canyon has been extensively studied, much less is known about the nature and origin of the carbonaceous aerosols that are present. This disparity in understanding arises from at least two causes: aerosol carbon data for the region are less plentiful and many of the sources that could contribute to that organic aerosol are both diverse and not well characterized. The objective of this present study is to examine the origin of the carbonaceous aerosol at Grand Canyon National Park during the summer season based on molecular tracer techniques applied to source and ambient samples collected specifically for this purpose.

  15. Modeling Activities in the Department of Energy’s Atmospheric Sciences Program

    SciTech Connect (OSTI)

    Fast, Jerome D.; Ghan, Steven J.; Schwartz, Stephen E.

    2009-03-01

    The Department of Energy's Atmospheric Science Program (ASP) conducts research pertinent to radiative forcing of climate change by atmospheric aerosols. The program consists of approximately 40 highly interactive peer-reviewed research projects that examine aerosol properties and processes and the evolution of aerosols in the atmosphere. Principal components of the program are instrument development, laboratory experiments, field studies, theoretical investigations, and modeling. The objectives of the Program are to 1) improve the understanding of aerosol processes associated with light scattering and absorption properties and interactions with clouds that affect Earth's radiative balance and to 2) develop model-based representations of these processes that enable the effects of aerosols on Earth's climate system to be properly represented in global-scale numerical climate models. Although only a few of the research projects within ASP are explicitly identified as primarily modeling activities, modeling actually comprises a substantial component of a large fraction of ASP research projects. This document describes the modeling activities within the Program as a whole, the objectives and intended outcomes of these activities, and the linkages among the several modeling components and with global-scale modeling activities conducted under the support of the Department of Energy's Climate Sciences Program and other aerosol and climate research programs.

  16. Amine-Amine Exchange in Aminium-Methanesulfonate Aerosols

    SciTech Connect (OSTI)

    Dawson, Matthew L.; Varner, Mychel E.; Perraud, Veronique M.; Ezell, Michael J.; Wilson, Jacqueline M.; Zelenyuk, Alla; Gerber, Robert B.; Finlayson-Pitts, Barbara J.

    2014-12-18

    Aerosol particles are ubiquitous in the atmosphere and have been shown to impact the Earth’s climate, reduce visibility, and adversely affect human health. Modeling the evolution of aerosol systems requires an understanding of the species and mechanisms involved in particle growth, including the complex interactions between particle- and gas-phase species. Here we report studies of displacement of amines (methylamine, dimethylamine or trimethylamine) in methanesulfonate salt particles by exposure to a different gas-phase amine, using a single particle mass spectrometer, SPLAT II. The variation of the displacement with the nature of the amine suggests that behavior is dependent on water in or on the particles. Small clusters of methanesulfonic acid with amines are used as a model in quantum chemical calculations to identify key structural elements that are expected to influence water uptake, and hence the efficiency of displacement by gas-phase molecules in the aminium salts. Such molecular-level understanding of the processes affecting the ability of gas-phase amines to displace particle-phase aminium species is important for modeling the growth of particles and their impacts in the atmosphere.

  17. Cloud Effects on Radiative Heating Rate Profiles over Darwin using ARM and A-train Radar/Lidar Observations

    SciTech Connect (OSTI)

    Thorsen, Tyler J.; Fu, Qiang; Comstock, Jennifer M.

    2013-06-11

    Observations of clouds from the ground-based U.S. Department of Energy Atmospheric Radiation Measurement program (ARM) and satellite-based A-train are used to compute cloud radiative forcing profiles over the ARM Darwin, Australia site. Cloud properties are obtained from both radar (the ARM Millimeter Cloud Radar (MMCR) and the CloudSat satellite in the A-train) and lidar (the ARM Micropulse lidar (MPL) and the Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observation (CALIPSO) satellite in the A-train) observations. Cloud microphysical properties are taken from combined radar and lidar retrievals for ice clouds and radar only or lidar only retrievals for liquid clouds. Large, statistically significant differences of up to 1.43 K/day exist between the mean ARM and A-train net cloud radiative forcing profiles. The majority of the difference in cloud radiative forcing profiles is shown to be due to a large difference in the cloud fraction above 12 km. Above this altitude the A-train cloud fraction is significantly larger because more clouds are detected by CALIPSO than by the ground-based MPL. It is shown that the MPL is unable to observe as many high clouds as CALIPSO due to being more frequently attenuated and a poorer sensitivity even in otherwise clear-sky conditions. After accounting for cloud fraction differences and instrument sampling differences due to viewing platform we determined that differences in cloud radiative forcing due to the retrieved ice cloud properties is relatively small. This study demonstrates that A-train observations are better suited for the calculation cloud radiative forcing profiles. In addition, we find that it is necessary to supplement CloudSat with CALIPSO observations to obtain accurate cloud radiative forcing profiles since a large portion of clouds at Darwin are detected by CALIPSO only.

  18. Examination of the Effects of Sea Salt Aerosols on Southeast Texas Ozone and Secondary Organic Aerosol 

    E-Print Network [OSTI]

    Benoit, Mark David

    2013-02-06

    of this research is to examine sea salt aerosols and their impact on polluted environments. Sea salt aerosols act as Cloud Condensation Nuclei (CCN) as well as providing a surface for heterogeneous reactions. Such reactions have implications for trace gases...

  19. Atmospheric Trace Gases from the Carbon Dioxide Information Analysis Center (CDIAC)

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    CDIAC products are indexed and searchable through a customized interface powered by ORNL's Mercury search engine. Products include numeric data packages, publications, trend data, atlases, models, etc. and can be searched for by subject area, keywords, authors, product numbers, time periods, collection sites, spatial references, etc. Some of the collections may also be included in the CDIAC publication, Trends Online: A Compendium of Global Change Data. Most data sets, many with numerous data files, are free to download from CDIAC's ftp area. The collections under the CDIAC heading of Atmospheric Trace Gases include: Atmospheric Carbon Dioxide, Atmospheric Methane, Atmospheric Carbon Monoxide, Atmospheric Hydrogen, Isotopes in Greenhouse Gases, Radionuclides, Aerosols, and Other Trace Gases.

  20. Urban aerosols and their variations with clouds and rainfall: A case study for New York and Houston

    E-Print Network [OSTI]

    Jin, Menglin

    warming (urban heat island effect (UHI)) and urban pollution impacts on surface energy budget have raisedUrban aerosols and their variations with clouds and rainfall: A case study for New York and Houston Shepherd Laboratory for Atmospheres, NASA Goddard Space Flight Center, Greenbelt, Maryland, USA Michael D

  1. Spatial distribution and size evolution of particles in Asian outflow: Significance of primary and secondary aerosols during ACE-Asia

    E-Print Network [OSTI]

    Clarke, Antony

    in the presence of pollution and mineral dust aerosol surface areas as high as 1200 mm2 cmŔ3 . Concentrations­13 nm % 5000 cmŔ3 ) in postfrontal air masses associated with offshore flow during cloud-free conditions Composition and Structure: Pollution--urban and regional (0305); 0368 Atmospheric Composition and Structure

  2. Clouds, aerosol, and precipitation in the Marine Boundary Layer: An ARM mobile facility deployment

    SciTech Connect (OSTI)

    Wood, Robert; Luke, Ed; Wyant, Matthew; Bretherton, Christopher S.; Remillard, Jasmine; Kollias, Pavlos; Fletcher, Jennifer; Stemmler, Jayson; deSzoeke, S.; Yuter, Sandra; Miller, Matthew; Mechem, David; Tselioudis, George; Chiu, Christine; Mann, Julia; O Connor, Ewan; Hogan, Robin; Dong, Xiquan; Miller, Mark; Ghate, Virendra; Jefferson, Anne; Min, Qilong; Minnis, Patrick; Palinkonda, Rabindra; Albrecht, Bruce; Hannay, Cecile; Lin, Yanluan

    2014-04-27

    The Clouds, Aerosol, and Precipitation in the Marine Boundary Layer (CAP-MBL) deployment at Graciosa Island in the Azores generated a 21-month (April 2009-December 2010) comprehensive dataset documenting clouds, aerosols, and precipitation using the Atmospheric Radiation Measurement Program (ARM) Mobile Facility (AMF). The scientific aim of the deployment is to gain improved understanding of the interactions of clouds, aerosols, and precipitation in the marine boundary layer. Graciosa Island straddles the boundary between the subtropics and midlatitudes in the Northeast Atlantic Ocean and consequently experiences a great diversity of meteorological and cloudiness conditions. Low clouds are the dominant cloud type, with stratocumulus and cumulus occurring regularly. Approximately half of all clouds contained precipitation detectable as radar echoes below the cloud base. Radar and satellite observations show that clouds with tops from 1-11 km contribute more or less equally to surface-measured precipitation at Graciosa. A wide range of aerosol conditions was sampled during the deployment consistent with the diversity of sources as indicated by back-trajectory analysis. Preliminary findings suggest important two-way interactions between aerosols and clouds at Graciosa, with aerosols affecting light precipitation and cloud radiative properties while being controlled in part by precipitation scavenging.The data from Graciosa are being compared with short-range forecasts made with a variety of models. A pilot analysis with two climate and two weather forecast models shows that they reproduce the observed time-varying vertical structure of lower-tropospheric cloud fairly well but the cloud-nucleating aerosol concentrations less well. The Graciosa site has been chosen to be a permanent fixed ARM site that became operational in October 2013.

  3. Clouds, aerosol, and precipitation in the Marine Boundary Layer: An ARM mobile facility deployment

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Wood, Robert; Luke, Ed; Wyant, Matthew; Bretherton, Christopher S.; Remillard, Jasmine; Kollias, Pavlos; Fletcher, Jennifer; Stemmler, Jayson; deSzoeke, S.; Yuter, Sandra; et al

    2014-04-27

    The Clouds, Aerosol, and Precipitation in the Marine Boundary Layer (CAP-MBL) deployment at Graciosa Island in the Azores generated a 21-month (April 2009-December 2010) comprehensive dataset documenting clouds, aerosols, and precipitation using the Atmospheric Radiation Measurement Program (ARM) Mobile Facility (AMF). The scientific aim of the deployment is to gain improved understanding of the interactions of clouds, aerosols, and precipitation in the marine boundary layer. Graciosa Island straddles the boundary between the subtropics and midlatitudes in the Northeast Atlantic Ocean and consequently experiences a great diversity of meteorological and cloudiness conditions. Low clouds are the dominant cloud type, with stratocumulusmore »and cumulus occurring regularly. Approximately half of all clouds contained precipitation detectable as radar echoes below the cloud base. Radar and satellite observations show that clouds with tops from 1-11 km contribute more or less equally to surface-measured precipitation at Graciosa. A wide range of aerosol conditions was sampled during the deployment consistent with the diversity of sources as indicated by back-trajectory analysis. Preliminary findings suggest important two-way interactions between aerosols and clouds at Graciosa, with aerosols affecting light precipitation and cloud radiative properties while being controlled in part by precipitation scavenging.The data from Graciosa are being compared with short-range forecasts made with a variety of models. A pilot analysis with two climate and two weather forecast models shows that they reproduce the observed time-varying vertical structure of lower-tropospheric cloud fairly well but the cloud-nucleating aerosol concentrations less well. The Graciosa site has been chosen to be a permanent fixed ARM site that became operational in October 2013.« less

  4. Spectro-Microscopic Measurements of Carbonaceous Aerosol Aging in Central California

    SciTech Connect (OSTI)

    Moffet, Ryan C.; Rodel, Tobias; Kelly, Stephen T.; Yu, Xiao-Ying; Carroll, Gregory; Fast, Jerome D.; Zaveri, Rahul A.; Laskin, Alexander; Gilles, Mary K.

    2013-10-29

    Carbonaceous aerosols are responsible for large uncertainties in climate models, degraded visibility, and adverse health effects. The Carbonaceous Aerosols and Radiative Effects Study (CARES) was designed to study carbonaceous aerosols in the natural environment of Central Valley, California, and learn more about their atmospheric formation and aging. This paper presents results from spectro-microscopic measurements of carbonaceous particles collected during CARES at the time of pollution accumulation event (June 27-29, 2010), when in situ measurements indicated an increase in the organic carbon content of aerosols as the Sacramento urban plume aged. Computer controlled scanning electron microscopy coupled with an energy dispersive X-ray detector (CCSEM/EDX) and scanning transmission X-ray microscopy coupled with near edge X-ray absorption spectroscopy (STXM/NEXAFS) were used to probe the chemical composition and morphology of individual particles. It was found that the mass of organic carbon on individual particles increased through condensation of secondary organic aerosol. STXM/NEXAFS indicated that the number fraction of homogenous organic particles lacking inorganic inclusions (greater than ~50 nm diameter) increased with plume age as did the organic mass per particle. Comparison of the CARES spectro-microscopic data set with a similar dataset obtained in Mexico City during the MILAGRO campaign showed that individual particles in Mexico City contained twice as much carbon as those sampled during CARES. The number fraction of soot particles at the Mexico City urban site (30%) was larger than at the CARES urban site (10%) and the most aged samples from CARES contained less carbon-carbon double bonds. Differences between carbonaceous particles in Mexico City and California result from different sources, photochemical conditions, gas phase reactants, and secondary organic aerosol precursors. The detailed results provided by these spectro-microscopic measurements will allow for a comprehensive evaluation of aerosol process models used in climate research.

  5. Evaluating WRF-Chem aerosol indirect effects in Southeast Pacific marine stratocumulus during VOCALS-REx

    SciTech Connect (OSTI)

    Saide P. E.; Springston S.; Spak, S. N.; Carmichael, G. R.; Mena-Carrasco, M. A.; Yang, Q.; Howell, S.; Leon, D. C.; Snider, J. R.; Bandy, A. R.; Collett, J. L.; Benedict, K. B.; de Szoeke, S. P.; Hawkins, L. N.; Allen, G.; Crawford, I.; Crosier, J.

    2012-03-29

    We evaluate a regional-scale simulation with the WRF-Chem model for the VAMOS (Variability of the American Monsoon Systems) Ocean-Cloud-Atmosphere-Land Study Regional Experiment (VOCALS-REx), which sampled the Southeast Pacific's persistent stratocumulus deck. Evaluation of VOCALS-REx ship-based and three aircraft observations focuses on analyzing how aerosol loading affects marine boundary layer (MBL) dynamics and cloud microphysics. We compare local time series and campaign-averaged longitudinal gradients, and highlight differences in model simulations with (W) and without (NW) wet deposition processes. The higher aerosol loadings in the NW case produce considerable changes in MBL dynamics and cloud microphysics, in accordance with the established conceptual model of aerosol indirect effects. These include increase in cloud albedo, increase in MBL and cloud heights, drizzle suppression, increase in liquid water content, and increase in cloud lifetime. Moreover, better statistical representation of aerosol mass and number concentration improves model fidelity in reproducing observed spatial and temporal variability in cloud properties, including top and base height, droplet concentration, water content, rain rate, optical depth (COD) and liquid water path (LWP). Together, these help to quantify confidence in WRF-Chem's modeled aerosol-cloud interactions, especially in the activation parameterization, while identifying structural and parametric uncertainties including: irreversibility in rain wet removal; overestimation of marine DMS and sea salt emissions, and accelerated aqueous sulfate conversion. Our findings suggest that WRF-Chem simulates marine cloud-aerosol interactions at a level sufficient for applications in forecasting weather and air quality and studying aerosol climate forcing, and may do so with the reliability required for policy analysis.

  6. Evaluating WRF-Chem aerosol indirect effects in Southeast Pacific marine stratocumulus during VOCALS-REx

    SciTech Connect (OSTI)

    Saide, Pablo; Spak, S. N.; Carmichael, Gregory; Mena-Carrasco, M. A.; Yang, Qing; Howell, S. G.; Leon, Dolislager; Snider, Jefferson R.; Bandy, Alan R.; Collett, Jeffrey L.; Benedict, K. B.; de Szoeke, S.; Hawkins, Lisa; Allen, Grant; Crawford, I.; Crosier, J.; Springston, S. R.

    2012-03-30

    We evaluate a regional-scale simulation with the WRF-Chem model for the VAMOS (Variability of the American Monsoon Systems) Ocean-Cloud-Atmosphere-Land Study Regional Experiment (VOCALS-REx), which sampled the Southeast Pacific's persistent stratocumulus deck. Evaluation of VOCALS-REx ship-based and aircraft observations focuses on analyzing how aerosol loading affects marine boundary layer (MBL) dynamics and cloud microphysics. We compare local time series and campaign averaged longitudinal gradients, and highlight differences in model simulations with (W) and without wet (NW) deposition processes. The higher aerosol loadings in the NW case produce considerable changes in MBL dynamics and cloud microphysics, in accordance with the established conceptual model of aerosol indirect effects. These include increase in cloud albedo, increase in MBL and cloud heights, drizzle suppression, increase in liquid water content, and increase in cloud lifetime. Moreover, better statistical representation of aerosol mass and number concentration improves model fidelity in reproducing observed spatial and temporal variability in cloud properties, including top and base height, droplet concentration, water content, rain rate, optical depth (COD) and liquid water path (LWP). Together, these help to quantify confidence in WRF-Chem's modeled aerosol-cloud interactions, while identifying structural and parametric uncertainties including: irreversibility in rain wet removal; overestimation of marine DMS and sea salt emissions and accelerated aqueous sulfate conversion. Our findings suggest that WRF-Chem simulates marine cloud-aerosol interactions at a level sufficient for applications in forecasting weather and air quality and studying aerosol climate forcing, including the reliability required for policy analysis and geo-engineering applications.

  7. An Aerosol Condensation Model for Sulfur Trioxide

    SciTech Connect (OSTI)

    Grant, K E

    2008-02-07

    This document describes a model for condensation of sulfuric acid aerosol given an initial concentration and/or source of gaseous sulfur trioxide (e.g. fuming from oleum). The model includes the thermochemical effects on aerosol condensation and air parcel buoyancy. Condensation is assumed to occur heterogeneously onto a preexisting background aerosol distribution. The model development is both a revisiting of research initially presented at the Fall 2001 American Geophysical Union Meeting [1] and a further extension to provide new capabilities for current atmospheric dispersion modeling efforts [2]. Sulfuric acid is one of the most widely used of all industrial chemicals. In 1992, world consumption of sulfuric acid was 145 million metric tons, with 42.4 Mt (mega-tons) consumed in the United States [10]. In 2001, of 37.5 Mt consumed in the U.S., 74% went into producing phosphate fertilizers [11]. Another significant use is in mining industries. Lawuyi and Fingas [7] estimate that, in 1996, 68% of use was for fertilizers and 5.8% was for mining. They note that H{sub 2}SO{sub 4} use has been and should continue to be very stable. In the United States, the elimination of MTBE (methyl tertiary-butyl ether) and the use of ethanol for gasoline production are further increasing the demand for petroleum alkylate. Alkylate producers have a choice of either a hydrofluoric acid or sulfuric acid process. Both processes are widely used today. Concerns, however, over the safety or potential regulation of hydrofluoric acid are likely to result in most of the growth being for the sulfuric acid process, further increasing demand [11]. The implication of sulfuric acid being a pervasive industrial chemical is that transport is also pervasive. Often, this is in the form of oleum tankers, having around 30% free sulfur trioxide. Although sulfuric acid itself is not a volatile substance, fuming sulfuric acid (referred to as oleum) is [7], the volatile product being sulfur trioxide. Sulfate aerosols and mist may form in the atmosphere on tank rupture. From chemical spill data from 1990-1996, Lawuyi02 and Fingas [7] prioritize sulfuric acid as sixth most serious. During this period, they note 155 spills totaling 13 Mt, out of a supply volume of 3700 Mt. Lawuyi and Fingas [7] summarize information on three major sulfuric acid spills. On 12 February 1984, 93 tons of sulfuric acid were spilled when 14 railroad cars derailed near MacTier, Parry Sound, Ontario. On 13 December 1978, 51 railroad cars derailed near Springhill, Nova Scotia. One car, containing 93% sulfuric acid, ruptured, spilling nearly its entire contents. In July 1993, 20 to 50 tons of fuming sulfuric acid spilled at the General Chemical Corp. plant in Richmond, California, a major industrial center near San Francisco. The release occurred when oleum was being loaded into a nonfuming acid railroad tank car that contained only a rupture disk as a safety device. The tank car was overheated and this rupture disk blew. The resulting cloud of sulfuric acid drifted northeast with prevailing winds over a number of populated areas. More than 3,000 people subsequently sought medical attention for burning eyes, coughing, headaches, and nausea. Almost all were treated and released on the day of the spill. By the day after the release, another 5,000 people had sought medical attention. The spill forced the closure of five freeways in the region as well as some Bay Area Rapid Transit System stations. Apart from corrosive toxicity, there is the additional hazard that the reactions of sulfur trioxide and sulfuric acid vapors with water are extremely exothermic [10, 11]. While the vapors are intrinsically denser than air, there is thus the likelihood of strong, warming-induced buoyancy from reactions with ambient water vapor, water-containing aerosol droplets, and wet environmental surface. Nordin [12] relates just such an occurrence following the Richmond, CA spill, with the plume observed to rise to 300 m. For all practical purposes, sulfur trioxide was the constituent released from the heated tank

  8. Modeling Study of the Effect of Anthropogenic Aerosols on Late Spring Drought in South China

    SciTech Connect (OSTI)

    Hu, Ning; Liu, Xiaohong

    2013-10-01

    In this study, the mechanisms underlying the decadal variability of late spring precipitation in south China are investigated using the latest version 1 of Community Earth System Model (CESM1). We aim to unravel the effects of different climate forcing agents, such as aerosols and greenhouse gases (GHGs), on the decadal variation of precipitation with transient experiments from pre-industry (for year 1850) to present-day (for year 2000). Our results reveal that: (1) CESM1 can reproduce the climatological features of atmospheric circulation and precipitation for the late spring in south China; (2) Only simulations including the forcing of anthropogenic aerosols can reproduce the observed decreasing trend of late spring precipitation from 1950-2000 in south China; (3) Aerosols affect the decadal change of precipitation mainly by altering the large scale atmospheric circulation, and to a less extent by increasing the lower-tropospheric stability to inhibit the convective precipitation; and (4) In comparison, other climate forcing agents, such as GHGs, have much smaller effects on the decadal change of spring precipitation in south China. Key words: precipitation, aerosols, climate change, south China, Community Earth System Model

  9. Aerosol Science and Technology, 43:641652, 2009 Copyright American Association for Aerosol Research

    E-Print Network [OSTI]

    Aerosol Science and Technology, 43:641­652, 2009 Copyright © American Association for Aerosol Differential Mobility Analyzer for Measurement of the Irreversibility of the Hygroscopic Growth Factor T is the irreversibility of the hygroscopic growth fac- tor of aerosol particles. The instrument uses the hysteresis

  10. Shortwave aerosol radiative forcing over cloud-free oceans from Terra: 1. Angular models for aerosols

    E-Print Network [OSTI]

    Christopher, Sundar A.

    Sensor Microwave Imager (SSM/I) data to obtain near surface wind speed. The new aerosol ADMs are built to obtain aerosol properties within a Clouds and Earth Radiant Energy System (CERES) footprint and Special as functions of near-surface ocean wind speed and MODIS aerosol optical depth at 0.55 mm (t0.55). Among the new

  11. Universal Spectrum for Atmospheric Suspended Particulates: Comparison with Observations

    E-Print Network [OSTI]

    A. M. Selvam

    2011-08-25

    Atmospheric flows exhibit self-similar fractal space-time fluctuations on all space-time scales in association with inverse power law distribution for power spectra of meteorological parameters such as wind, temperature, etc., and thus implies long-range correlations, identified as self-organized criticality generic to dynamical systems in nature. A general systems theory based on classical statistical physical concepts developed by the author visualizes the fractal fluctuations to result from the coexistence of eddy fluctuations in an eddy continuum, the larger scale eddies being the integrated mean of enclosed smaller scale eddies. The model satisfies the maximum entropy principle and predicts that the probability distributions of component eddy amplitudes and the corresponding variances (power spectra) are quantified by the same universal inverse power law distribution which is a function of the golden mean. Atmospheric particulates are held in suspension by the vertical velocity distribution (spectrum). The atmospheric particulate size spectrum is derived in terms of the model predicted universal inverse power law characterizing atmospheric eddy spectrum. Model predicted spectrum is in agreement with the following four experimentally determined data sets: (i) CIRPAS mission TARFOX_WALLOPS_SMPS aerosol size distributions (ii) CIRPAS mission ARM-IOP (Ponca City, OK) aerosol size distributions (iii) SAFARI 2000 CV-580 (CARG Aerosol and Cloud Data) cloud drop size distributions and (iv) TWP-ICE (Darwin, Australia) rain drop size distributions.

  12. Researchers Model Impact of Aerosols Over California

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    Impact of Aerosols Over California Research may clarify the effectiveness of regional pollution controls May 28, 2013 | Tags: Climate Research, Hopper Contact: Linda Vu,...

  13. Aerosol Retrieval Using Remote-sensed Observations

    E-Print Network [OSTI]

    Wang, Yueqing

    2012-01-01

    4.1.2 Baltimore and the DRAGONaround Baltimore . . . . . . . . . . . . . . . . . . . 4.1.4component aerosol 1 for Baltimore-Washington region on June

  14. A 350-year atmospheric history for carbonyl sulfide inferred from Antarctic firn air and air trapped in ice

    E-Print Network [OSTI]

    Saltzman, Eric

    A 350-year atmospheric history for carbonyl sulfide inferred from Antarctic firn air and air August 2004; published 17 November 2004. [1] Carbonyl sulfide (COS) and other trace gases were measured: atmosphere composition, carbonyl sulfide, stratosphere sulfate aerosol Citation: Montzka, S. A., M. Aydin, M

  15. Building America Webinar: Sealing of Home Enclosures with Aerosol...

    Energy Savers [EERE]

    Sealing of Home Enclosures with Aerosol Particles Building America Webinar: Sealing of Home Enclosures with Aerosol Particles This webinar was presented by research team Building...

  16. Investigation of warm-cloud microphysics using a multi-component cloud model: Interactive effects of the aerosol spectrum. Master's thesis

    SciTech Connect (OSTI)

    Zahn, S.G.

    1993-12-01

    Clouds, especially low, warm, boundary-layer clouds, play an important role in regulating the earth's climate due to their significant contribution to the global albedo. The radiative effects of individual clouds are controlled largely by cloud microstructure, which is itself sensitive to the concentration and spectral distribution of the atmospheric aerosol. Increases in aerosol particle concentrations from anthropogenic activity could result in increased cloud albedo and global cloudiness, increasing the amount of reflected solar radiation. However, the effects of increased aerosol particle concentrations could be offset by the presence of giant or ultragiant aerosol particles. A one-dimensional, multi-component microphysical cloud model has been used to demonstrate the effects of aerosol particle spectral variations on the microstructure of warm clouds. Simulations performed with this model demonstrate that the introduction of increased concentrations of giant aerosol particles has a destabilizing effect on the cloud microstructure. Also, it is shown that warm-cloud microphysical processes modify the aerosol particle spectrum, favoring the generation of the largest sized particles via the collision-coalescence process. These simulations provide further evidence that the effect of aerosol particles on cloud microstructure must be addressed when considering global climate forecasts.

  17. Improving Bulk Microphysics Parameterizations in Simulations of Aerosol Effects

    SciTech Connect (OSTI)

    Wang, Yuan; Fan, Jiwen; Zhang, Renyi; Leung, Lai-Yung R.; Franklin, Charmaine N.

    2013-06-05

    To improve the microphysical parameterizations for simulations of the aerosol indirect effect (AIE) in regional and global climate models, a double-moment bulk microphysical scheme presently implemented in the Weather Research and Forecasting (WRF) model is modified and the results are compared against atmospheric observations and simulations produced by a spectral bin microphysical scheme (SBM). Rather than using prescribed aerosols as in the original bulk scheme (Bulk-OR), a prognostic doublemoment aerosol representation is introduced to predict both the aerosol number concentration and mass mixing ratio (Bulk-2M). The impacts of the parameterizations of diffusional growth and autoconversion and the selection of the embryonic raindrop radius on the performance of the bulk microphysical scheme are also evaluated. Sensitivity modeling experiments are performed for two distinct cloud regimes, maritime warm stratocumulus clouds (SC) over southeast Pacific Ocean from the VOCALS project and continental deep convective clouds (DCC) in the southeast of China from the Department of Energy/ARM Mobile Facility (DOE/AMF) - China field campaign. The results from Bulk-2M exhibit a much better agreement in the cloud number concentration and effective droplet radius in both the SC and DCC cases with those from SBM and field measurements than those from Bulk-OR. In the SC case particularly, Bulk-2M reproduces the observed drizzle precipitation, which is largely inhibited in Bulk-OR. Bulk-2M predicts enhanced precipitation and invigorated convection with increased aerosol loading in the DCC case, consistent with the SBM simulation, while Bulk-OR predicts the opposite behaviors. Sensitivity experiments using four different types of autoconversion schemes reveal that the autoconversion parameterization is crucial in determining the raindrop number, mass concentration, and drizzle formation for warm 2 stratocumulus clouds. An embryonic raindrop size of 40 ?m is determined as a more realistic setting in the autoconversion parameterization. The saturation adjustment employed in calculating condensation/evaporation in the bulk scheme is identified as the main factor responsible for the large discrepancies in predicting cloud water in the SC case, suggesting that an explicit calculation of diffusion growth with predicted supersaturation is necessary for further improvements of the bulk microphysics scheme. Lastly, a larger rain evaporation rate below cloud is found in the bulk scheme in comparison to the SBM simulation, which could contribute to a lower surface precipitation in the bulk scheme.

  18. FY 2010 Fourth Quarter Report: Evaluation of the Dependency of Drizzle Formation on Aerosol Properties

    SciTech Connect (OSTI)

    Lin, W; McGraw, R; Liu, Y; Wang, J; Vogelmann, A; Daum, PH

    2010-10-01

    Metric for Quarter 4: Report results of implementation of composite parameterization in single-column model (SCM) to explore the dependency of drizzle formation on aerosol properties. To better represent VOCALS conditions during a test flight, the Liu-Duam-McGraw (LDM) drizzle parameterization is implemented in the high-resolution Weather Research and Forecasting (WRF) model, as well as in the single-column Community Atmosphere Model (CAM), to explore this dependency.

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

    SciTech Connect (OSTI)

    Mahajan, Salil [ORNL; Evans, Katherine J [ORNL; Hack, James J [ORNL; Truesdale, John [National Center for Atmospheric Research (NCAR)

    2013-01-01

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

  20. Atmospheric Radiation Measurement (ARM) Data from Los Angeles, California, to Honolulu, Hawaii for the Marine ARM GPCI Investigation of Clouds (MAGIC) Field Campaign (an AMF2 Deployment)

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    From October 2012 through September 2013, the second ARM Mobile Facility (AMF2) was deployed on the container ship Spirit, operated by Horizon Lines, for the Marine ARM GPCI* Investigation of Clouds (MAGIC) field campaign. During approximately 20 round trips between Los Angeles, California, and Honolulu, Hawaii, AMF2 obtained continuous on-board measurements of cloud and precipitation, aerosols, and atmospheric radiation; surface meteorological and oceanographic variables; and atmospheric profiles from weather balloons launched every six hours. During two two-week intensive observational periods in January and July 2013, additional instruments were deployed and balloon soundings were be increased to every three hours. These additional data provided a more detailed characterization of the state of the atmosphere and its daily cycle during two distinctly different seasons. The primary objective of MAGIC was to improve the representation of the stratocumulus-to-cumulus transition in climate models. AMF2 data documented the small-scale physical processes associated with turbulence, convection, and radiation in a variety of marine cloud types.

  1. Carbonaceous Aerosol Study Using Advanced Particle Instrumentation

    E-Print Network [OSTI]

    Qi, Li

    2010-01-01

    6 6.1 Introduction Biomass combustion emissions contributeEmissions of trace gases and aerosols during the open combustion of biomassbiomass burning work explored the evolution of organic aerosol emissions as a function of modified combustion efficiency with correlations drawn between levoglucosan emissions

  2. Optimal Estimation Retrieval Aerosol Microphysical Properties

    E-Print Network [OSTI]

    Oxford, University of

    ) the validation of this algorithm on the basis of synthetic extinction data, and (3) application of the new algorithm to SAGE II measurements of stratospheric background aerosol. The validation results indicate that the new method is able to retrieve the particle size of typical background aerosols reasonably well

  3. Aerosol Properties from Multi-spectral and Multi-angular Aircraft 4STAR Observations: Expected Advantages and Challenges

    SciTech Connect (OSTI)

    Kassianov, Evgueni I.; Flynn, Connor J.; Redemann, Jens; Schmid, Beat; Russell, P. B.; Sinyuk, Alexander

    2012-11-01

    The airborne Spectrometer for Sky-Scanning, Sun-Tracking Atmospheric Research (4STAR) is developed to retrieve aerosol microphysical and optical properties from multi-angular and multi-spectral measurements of sky radiance and direct-beam sun transmittance. The necessarily compact design of the 4STAR may cause noticeable apparent enhancement of sky radiance at small scattering angles. We assess the sensitivity of expected 4STAR-based aerosol retrieval to such enhancement by applying the operational AERONET retrieval code and constructed synthetic 4STARlike data. Also, we assess the sensitivity of the broadband fluxes and the direct aerosol radiative forcing to uncertainties in aerosol retrievals associated with the sky radiance enhancement. Our sensitivity study results suggest that the 4STARbased aerosol retrieval has limitations in obtaining detailed information on particle size distribution and scattering phase function. However, these limitations have small impact on the retrieved bulk optical parameters, such as the asymmetry factor (up to 4%, or ±0.02) and single-scattering albedo (up to 2%, or ±0.02), and the calculated direct aerosol radiative forcing (up to 6%, or 2 Wm-2).

  4. Chemical Composition and Sources of Coastal Marine Aerosol Particles during the 2008 VOCALS-REx Campaign

    SciTech Connect (OSTI)

    Lee, Y.- N.; Springston, S.; Jayne, John T.; Wang, Jian; Hubbe, John M.; Senum, Gunnar I.; Kleinman, Lawrence I.; Daum, Peter H.

    2014-05-23

    The chemical composition of aerosol particles (Dp 1.5 ?m) was measured over the southeast Pacific Ocean during the VAMOS (Variability of the American Monsoon Systems) Ocean-Cloud-Atmosphere-Land Study Regional Experiment (VOCALS-Rex) between 16 October and 15 November 2008 using the US Department of Energy (DOE) G-1 aircraft. The objective of these flights was to gain an understanding of the sources and evolution of these aerosols, and of how they interact with the marine stratus cloud layer that prevails in this region of the globe. Our measurements showed that the marine boundary layer (MBL) aerosol mass was dominated by non-sea-salt SO2?4, followed by Na+, Cl?, Org (total organics), NH+4 , and NO?3 , in decreasing order of importance; CH3SO?3 (MSA), Ca2+, and K+ rarely exceeded their limits of detection. Aerosols were strongly acidic with a NH+4 to SO2?4 equivalents ratio typically < 0.3. Sea-salt aerosol (SSA) particles, represented by NaCl, exhibited Cl? deficits caused by both HNO3 and H2SO4, but for the most part were externally mixed with particles, mainly SO2?4. SSA contributed only a small fraction of the total accumulation mode particle number concentration. It was inferred that all aerosol species (except SSA) were of predominantly continental origin because of their strong land-to-sea concentration gradient. Comparison of relative changes in median values suggests that (1) an oceanic source of NH3 is present between 72° W and 76° W, (2) additional organic aerosols from biomass burns or biogenic precursors were emitted from coastal regions south of 31° S, with possible cloud processing, and (3) free tropospheric (FT) contributions to MBL gas and aerosol concentrations were negligible. The very low levels of CH3SO?3 observed as well as the correlation between SO2?4 and NO?3 (which is thought primarily anthropogenic) suggest a limited contribution of DMS to SO2?4 aerosol production during VOCALS.

  5. AEROSOL PARTICLE COLLECTOR DESIGN STUDY

    SciTech Connect (OSTI)

    Lee, S; Richard Dimenna, R

    2007-09-27

    A computational evaluation of a particle collector design was performed to evaluate the behavior of aerosol particles in a fast flowing gas stream. The objective of the work was to improve the collection efficiency of the device while maintaining a minimum specified air throughput, nominal collector size, and minimal power requirements. The impact of a range of parameters was considered subject to constraints on gas flow rate, overall collector dimensions, and power limitations. Potential improvements were identified, some of which have already been implemented. Other more complex changes were identified and are described here for further consideration. In addition, fruitful areas for further study are proposed.

  6. ARM Cloud Aerosol Precipitation Experiment

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity ofkandz-cm11 OutreachProductswsicloudwsicloudden Documentation Data Management Facility PlotsProducts (VAP) VAP38 ARM6Aerosol

  7. Impacts of aerosol-cloud interactions on past and future changes in tropospheric composition

    SciTech Connect (OSTI)

    Unger, N.; Menon, S.; Shindell, D. T.; Koch, D. M.

    2009-02-02

    The development of effective emissions control policies that are beneficial to both climate and air quality requires a detailed understanding of all the feedbacks in the atmospheric composition and climate system. We perform sensitivity studies with a global atmospheric composition-climate model to assess the impact of aerosols on tropospheric chemistry through their modification on clouds, aerosol-cloud interactions (ACI). The model includes coupling between both tropospheric gas-phase and aerosol chemistry and aerosols and liquid-phase clouds. We investigate past impacts from preindustrial (PI) to present day (PD) and future impacts from PD to 2050 (for the moderate IPCC A1B scenario) that embrace a wide spectrum of precursor emission changes and consequential ACI. The aerosol indirect effect (AIE) is estimated to be -2.0 Wm{sup -2} for PD-PI and -0.6 Wm{sup -2} for 2050-PD, at the high end of current estimates. Inclusion of ACI substantially impacts changes in global mean methane lifetime across both time periods, enhancing the past and future increases by 10% and 30%, respectively. In regions where pollution emissions increase, inclusion of ACI leads to 20% enhancements in in-cloud sulfate production and {approx}10% enhancements in sulfate wet deposition that is displaced away from the immediate source regions. The enhanced in-cloud sulfate formation leads to larger increases in surface sulfate across polluted regions ({approx}10-30%). Nitric acid wet deposition is dampened by 15-20% across the industrialized regions due to ACI allowing additional re-release of reactive nitrogen that contributes to 1-2 ppbv increases in surface ozone in outflow regions. Our model findings indicate that ACI must be considered in studies of methane trends and projections of future changes to particulate matter air quality.

  8. AEROSOL ABSORPTION IN CLOUDY SCENES USING PASSIVE SATELLITE INSTRUMENTS

    E-Print Network [OSTI]

    Graaf, Martin de

    AEROSOL ABSORPTION IN CLOUDY SCENES USING PASSIVE SATELLITE INSTRUMENTS M. de Graaf, L.G. Tilstra information has become available from active space-based sensors and some dedicated field campaigns on aerosol-absorption, is the Absorbing Aerosol Index (AAI), which can indicate absorbing aerosols overlying clouds. The AAI is available

  9. Pathways of sulfate enhancement by natural and anthropogenic mineral aerosols in China

    SciTech Connect (OSTI)

    Huang, Xin [Peking Univ., Beijing (China); Song, Yu [Peking Univ., Beijing (China); Zhao, Chun [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Li, Mengmeng [Peking Univ., Beijing (China); Zhu, Tong [Peking Univ., Beijing (China); Zhang, Qiang [Tsinghua Univ., Beijing (China); Zhang, Xiaoye [Chinese Academy of Meteorological Sciences, CMA, Beijing (China)

    2014-12-27

    China, the world’s largest consumer of coal, emits approximately 30 million tons of sulfur dioxide (SO?) per year. SO? is subsequently oxidized to sulfate in the atmosphere. However, large gaps exist between model-predicted and measured sulfate levels in China. Long-term field observations and numerical simulations were integrated to investigate the effect of mineral aerosols on sulfate formation. We found that mineral aerosols contributed a nationwide average of approximately 22% to sulfate production in 2006. The increased sulfate concentration was approximately 2 ?g m?ł in the entire China. In East China and the Sichuan Basin, the increments reached 6.3 ?g m?ł and 7.3 ?g m?ł, respectively. Mineral aerosols led to faster SO? oxidation through three pathways. First, more SO? was dissolved as cloud water alkalinity increased due to water-soluble mineral cations. Sulfate production was then enhanced through the aqueous-phase oxidation of S(IV) (dissolved sulfur in oxidation state +4). The contribution to the national sulfate production was 5%. Second, sulfate was enhanced through S(IV) catalyzed oxidation by transition metals. The contribution to the annual sulfate production was 8%, with 19% during the winter that decreased to 2% during the summer. Third, SO? reacts on the surface of mineral aerosols to produce sulfate. The contribution to the national average sulfate concentration was 9% with 16% during the winter and a negligible effect during the summer. The inclusion of mineral aerosols does resolve model discrepancies with sulfate observations in China, especially during the winter. These three pathways, which are not fully considered in most current chemistry-climate models, will significantly impact assessments regarding the effects of aerosol on climate change in China.

  10. Understanding oxygen photochemistry in CO2-dominated planetary atmospheres

    E-Print Network [OSTI]

    Strong, Kimberly

    of confidence in forecasting the temperature profile for the Martian atmosphere over the aerobraking region temperature, dust load, water concentrations, etc., on the vertical ii #12;structure of the emissions the NO airglow emission in the Mars atmosphere from the SPICAM instrument. The method is tested with one year

  11. Aerosol optical hygroscopicity measurements during the 2010 CARES campaign

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Atkinson, D. B.; Radney, J. G.; Lum, J.; Kolesar, K. R.; Cziczo, D. J.; Pekour, M. S.; Zhang, Q.; Setyan, A.; Zelenyuk, A.; Cappa, C. D.

    2015-04-17

    Measurements of the effect of water uptake on particulate light extinction or scattering made at two locations during the 2010 Carbonaceous Aerosols and Radiative Effects Study (CARES) study around Sacramento, CA are reported. The observed influence of water uptake, characterized through the dimensionless optical hygroscopicity parameter ?, is compared with calculations constrained by observed particle size distributions and size-dependent particle composition. A closure assessment has been carried out that allowed for determination of the average hygroscopic growth factors (GFs) at 85% relative humidity and the dimensionless hygroscopicity parameter ? for oxygenated organic aerosol (OA) and for supermicron particles (defined heremore »as particles with aerodynamic diameters between 1 and 2.5 microns), yielding ? = 0.1–0.15 and 0.9–1.0, respectively. The derived range of oxygenated OA ? values are in line with previous observations. The relatively large values for supermicron particles is consistent with substantial contributions of sea-salt-containing particles in this size range. Analysis of time-dependent variations in the supermicron particle hygroscopicity suggest that atmospheric processing, specifically chloride displacement by nitrate and the accumulation of secondary organics on supermicron particles, can lead to substantial depression of the observed GF.« less

  12. Studying trends in biomass burning aerosol using the Absorbing Aerosol Index derived from GOME, SCIAMACHY, and GOME-2

    E-Print Network [OSTI]

    Tilstra, Gijsbert

    Studying trends in biomass burning aerosol using the Absorbing Aerosol Index derived from GOME the resulting time series, we use tropospheric NO2 data as a reference in the regions dominated by biomass sensitive to desert dust aerosols (DDA) and biomass burning aerosols (BBA). See Figure 1. The AAI

  13. Removal of Sarin Aerosol and Vapor by Water Sprays

    SciTech Connect (OSTI)

    Brockmann, John E.

    1998-09-01

    Falling water drops can collect particles and soluble or reactive vapor from the gas through which they fall. Rain is known to remove particles and vapors by the process of rainout. Water sprays can be used to remove radioactive aerosol from the atmosphere of a nuclear reactor containment building. There is a potential for water sprays to be used as a mitigation technique to remove chemical or bio- logical agents from the air. This paper is a quick-look at water spray removal. It is not definitive but rather provides a reasonable basic model for particle and gas removal and presents an example calcu- lation of sarin removal from a BART station. This work ~ a starting point and the results indicate that further modeling and exploration of additional mechanisms for particle and vapor removal may prove beneficial.

  14. Raman Lidar Profiles–Temperature (RLPROFTEMP) Value-Added Product

    SciTech Connect (OSTI)

    Newsom, RK; Sivaraman, C; McFarlane, SA

    2012-10-31

    The purpose of this document is to describe the Raman Lidar Profiles–Temperature (RLPROFTEMP) value-added product (VAP) and the procedures used to derive atmospheric temperature profiles from the raw RL measurements. Sections 2 and 4 describe the input and output variables, respectively. Section 3 discusses the theory behind the measurement and the details of the algorithm, including calibration and overlap correction.

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

    SciTech Connect (OSTI)

    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.

  16. Long-term impacts of aerosols on the vertical development of clouds and precipitation

    SciTech Connect (OSTI)

    Li, Zhanqing; Niu, F.; Fan, Jiwen; Liu, Yangang; Rosenfeld, Daniel; Ding, Yanni

    2011-12-01

    Aerosol has complex effects on clouds and precipitation that may augment or offset each other contingent upon a variety of variables. As a result, its long-term impact on climate is largely unknown. Using 10 years of the US Atmospheric Radiation Measurement (ARM) measurements, strong aerosol effects of climatologically significance are detected. With increasing total aerosol number concentration (condensation nucleus, CN) measured near the ground, both cloud top height and precipitation change systematically for mix-phase clouds of warm-base (cloud base <1km) and cold-top (above the freezing level), but not for pure liquid and ice clouds. Cloud thickness can increase systematically with the CN concentration by up to a factor of 2. The response of precipitation to CN depends on cloud liquid water path (LWP). As CN increases, rain occurs more frequently for high LWP but less frequently for low LWP. Such strong signals of aerosol long-term impact on cloud and precipitation have not been reported and have significant implications for climate change studies, especially concerning regional and global climate change induced by pollution.

  17. PUBLISHED ONLINE: 28 FEBRUARY 2010 | DOI: 10.1038/NGEO778 Atmospheric nanoparticles formed from

    E-Print Network [OSTI]

    and heterogeneous reactions of organics. However, particles in the nucleation mode (subject to a large simulations of new particle formation. Atmospheric aerosols impair visibility, alter the radiative balance. Considerable efforts have been devoted to understanding the processes governing new particle formation

  18. Estimates of atmospheric dry deposition and associated input of nutrients to Gulf of Aqaba seawater

    E-Print Network [OSTI]

    Jacobson, Mark

    and subsequently low- ered atmospheric CO2 level during that period [Martin, 1990; Mahowald et al., 1999; Bopp et and September 2005. The main inorganic N compounds in the water soluble fraction of aerosol particles were in other seasons. The inorganic N/P molar ratios in the seawater-soluble fraction of the dry deposition

  19. BNL-67852-AB CHARACTERIZATION OF ORGANICS IN ATMOSPHERIC PARTICLES BY SINGLE

    E-Print Network [OSTI]

    the fundamental processes, which constitute the "aerosol atmospheric life cycle", i.e., primary emission at present to evaporate and ionize the components for time of flight mass spectroscopic analysis. SPLAT. The resolving power of the instrument in mass-to-charge units is 1000. The TOF- MS spectra are digitized

  20. Project Overview: Cumulus Humilis Aerosol Processing Study (CHAPS): Proposed Summer 2007 ASP Field Campaign

    SciTech Connect (OSTI)

    Berkowitz, Carl M.; Berg, Larry K.; Ogren, J. A.; Hostetler, Chris A.; Ferrare, Richard

    2006-05-18

    This white paper presents the scientific motivation and preliminary logistical plans for a proposed ASP field campaign to be carried out in the summer of 2007. The primary objective of this campaign is to use the DOE Gulfstream-1 aircraft to make measurements characterizing the chemical, physical and optical properties of aerosols below, within and above large fields of fair weather cumulus and to use the NASA Langley Research Center’s High Spectral Resolution Lidar (HSRL) to make independent measurements of aerosol backscatter and extinction profiles in the vicinity of these fields. Separate from the science questions to be addressed by these observations will be information to add in the development of a parameterized cumulus scheme capable of including multiple cloud fields within a regional or global scale model. We will also be able to compare and contrast the cloud and aerosol properties within and outside the Oklahoma City plume to study aerosol processes within individual clouds. Preliminary discussions with the Cloud and Land Surface Interaction Campaign (CLASIC) science team have identified overlap between the science questions posed for the CLASIC Intensive Operation Period (IOP) and the proposed ASP campaign, suggesting collaboration would benefit both teams.

  1. Lidar Measurements of the Vertical Distribution of Aerosol Optical and Physical Properties over Central Asia

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Chen, Boris B.; Sverdlik, Leonid G.; Imashev, Sanjar A.; Solomon, Paul A.; Lantz, Jeffrey; Schauer, James J.; Shafer, Martin M.; Artamonova, Maria S.; Carmichael, Gregory R.

    2013-01-01

    The vertical structure of aerosol optical and physical properties was measured by Lidar in Eastern Kyrgyzstan, Central Asia, from June 2008 to May 2009. Lidar measurements were supplemented with surface-based measurements of PM 2.5 and PM 10 mass and chemical composition in both size fractions. Dust transported into the region is common, being detected 33% of the time. The maximum frequency occurred in the spring of 2009. Dust transported to Central Asia comes from regional sources, for example, Taklimakan desert and Aral Sea basin, and from long-range transport, for example, deserts of Arabia, Northeast Africa, Iran, and Pakistan. Regionalmore »sources are characterized by pollution transport with maximum values of coarse particles within the planetary boundary layer, aerosol optical thickness, extinction coefficient, integral coefficient of aerosol backscatter, and minimum values of the Ĺngström exponent. Pollution associated with air masses transported over long distances has different characteristics during autumn, winter, and spring. During winter, dust emissions were low resulting in high values of the Ĺngström exponent (about 0.51) and the fine particle mass fraction (64%). Dust storms were more frequent during spring with an increase in coarse dust particles in comparison to winter. The aerosol vertical profiles can be used to lower uncertainty in estimating radiative forcing. « less

  2. Ozone Profile Retrieval from an Advanced Infrared Sounder: Experiments with Tropopause-Based Climatology and Optimal Estimation Approach

    E-Print Network [OSTI]

    Pan, Laura

    Ozone Profile Retrieval from an Advanced Infrared Sounder: Experiments with Tropopause for retrieving atmospheric ozone profile information from advanced satellite infrared sounders, this study investigates various methods to optimize ozone retrievals. A set of retrieval experiments has been performed

  3. Lidar Investigation of Tropical Nocturnal Boundary Layer Aerosols and Cloud Macrophysics

    SciTech Connect (OSTI)

    Manoj, M. G.; Devara, PC S.; Taraphdar, Sourav

    2013-10-01

    Observational evidence of two-way association between nocturnal boundary layer aerosols and cloud macrophysical properties under different meteorological conditions is reported in this paper. The study has been conducted during 2008-09 employing a high space-time resolution polarimetric micro-pulse lidar over a tropical urban station in India. Firstly, the study highlights the crucial role of boundary layer aerosols and background meteorology on the formation and structure of low-level stratiform clouds in the backdrop of different atmospheric stability conditions. Turbulent mixing induced by the wind shear at the station, which is associated with a complex terrain, is found to play a pivotal role in the formation and structural evolution of nocturnal boundary layer clouds. Secondly, it is shown that the trapping of energy in the form of outgoing terrestrial radiation by the overlying low-level clouds can enhance the aerosol mixing height associated with the nocturnal boundary layer. To substantiate this, the long-wave heating associated with cloud capping has been quantitatively estimated in an indirect way by employing an Advanced Research Weather Research and Forecasting (WRF-ARW) model version 2.2 developed by National Center for Atmospheric Research (NCAR), Colorado, USA, and supplementary data sets; and differentiated against other heating mechanisms. The present investigation as well establishes the potential of lidar remote-sensing technique in exploring some of the intriguing aspects of the cloud-environment relationship.

  4. Aerosol, Cloud, and Climate: From Observation to Model (457th Brookhaven Lecture)

    ScienceCinema (OSTI)

    Wang, Jian [Ph.D., Environmental Sciences Department

    2010-09-01

    In the last 100 years, the Earth has warmed by about 1şF, glaciers and sea ice have been melting more quickly than previously, especially during the past decade, and the level of the sea has risen about 6-8 inches worldwide. Scientists have long been investigating this phenomenon of ?global warming,? which is believed to be at least partly due to the increased carbon dioxide (CO2) concentration in the air from burning fossil fuels. Funded by DOE, teams of researchers from BNL and other national labs have been gathering data in the U.S. and internationally to build computer models of climate and weather to help in understanding general patterns, causes, and perhaps, solutions. Among many findings, researchers observed that atmospheric aerosols, minute particles in the atmosphere, can significantly affect global energy balance and climate. Directly, aerosols scatter and absorb sunlight. Indirectly, increased aerosol concentration can lead to smaller cloud droplets, changing clouds in ways that tend to cool global climate and potentially mask overall warming from man-made CO2.

  5. Aerosol, Cloud, and Climate: From Observation to Model (457th Brookhaven Lecture)

    SciTech Connect (OSTI)

    Wang, Jian (Ph.D., Environmental Sciences Department) [Ph.D., Environmental Sciences Department

    2010-05-12

    In the last 100 years, the Earth has warmed by about 1şF, glaciers and sea ice have been melting more quickly than previously, especially during the past decade, and the level of the sea has risen about 6-8 inches worldwide. Scientists have long been investigating this phenomenon of “global warming,” which is believed to be at least partly due to the increased carbon dioxide (CO2) concentration in the air from burning fossil fuels. Funded by DOE, teams of researchers from BNL and other national labs have been gathering data in the U.S. and internationally to build computer models of climate and weather to help in understanding general patterns, causes, and perhaps, solutions. Among many findings, researchers observed that atmospheric aerosols, minute particles in the atmosphere, can significantly affect global energy balance and climate. Directly, aerosols scatter and absorb sunlight. Indirectly, increased aerosol concentration can lead to smaller cloud droplets, changing clouds in ways that tend to cool global climate and potentially mask overall warming from man-made CO2.

  6. Aerosol Condensational Growth in Cloud Formation 

    E-Print Network [OSTI]

    Geng, Jun

    2010-10-12

    A code for the quasi-stationary solution of the coupled heat and mass transport equations for aerosols in a finite volume was developed. Both mass and heat are conserved effectively in the volume, which results in a ...

  7. Aerosol fabrication methods for monodisperse nanoparticles

    DOE Patents [OSTI]

    Jiang, Xingmao; Brinker, C Jeffrey

    2014-10-21

    Exemplary embodiments provide materials and methods for forming monodisperse particles. In one embodiment, the monodisperse particles can be formed by first spraying a nanoparticle-containing dispersion into aerosol droplets and then heating the aerosol droplets in the presence of a shell precursor to form core-shell particles. By removing either the shell layer or the nanoparticle core of the core-shell particles, monodisperse nanoparticles can be formed.

  8. Electrically Driven Technologies for Radioactive Aerosol Abatement

    SciTech Connect (OSTI)

    David W. DePaoli; Ofodike A. Ezekoye; Costas Tsouris; Valmor F. de Almeida

    2003-01-28

    The purpose of this research project was to develop an improved understanding of how electriexecy driven processes, including electrocoalescence, acoustic agglomeration, and electric filtration, may be employed to efficiently treat problems caused by the formation of aerosols during DOE waste treatment operations. The production of aerosols during treatment and retrieval operations in radioactive waste tanks and during thermal treatment operations such as calcination presents a significant problem of cost, worker exposure, potential for release, and increased waste volume.

  9. Development of plutonium aerosol fractionation system 

    E-Print Network [OSTI]

    Mekala, Malla R.

    1993-01-01

    DEVELOPMENT OF A PLUTONIUM AEROSOL FRACTIONATION SYSTEM A Thesis by MALLA R. MEKALA Submitted to the Office of Graduate Studies of Texas A&M University in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE August... 1993 Major Subject: Mechanical Engineering DEVELOPMENT OP A PLUTONIUM AEROSOL FRACTIONATION SYSTEM A Thesis by MALLA R. MEKALA Approved as to style and content by: A. R. McFarland (Chair of Committee) N. K. Anand (Mer toer) (', & C. B...

  10. Optical Properties of Secondary Organic Aerosols

    E-Print Network [OSTI]

    Kim, Hwajin

    2012-01-01

    J. H. Journal of Atmospheric Chemistry 1997 , 26, 189-193. (induced ageing, Atmospheric Chemistry and Physics, 11(21),emerging issues, Atmospheric Chemistry and Physics, 9(14),

  11. Secondary Organic Aerosol Formation From Aromatic Hydrocarbon

    E-Print Network [OSTI]

    Tang, Ping

    2013-01-01

    Sources and Role in Atmospheric Chemistry. Science 276,2.5. Journal of Atmospheric Chemistry 47, 79–100. Kleinman,toluene and benzene. Atmospheric Chemistry and Physics 7,

  12. Aerosol-cloud radiative effects from passive satellite instruments Mar%n de Graaf

    E-Print Network [OSTI]

    Graaf, Martin de

    Satellite measurements of absorbing aerosols Reflectance Difference Method Cloud modelling Results Outlook Aerosol-Radiation Interac. Aerosol-Cloud Interac. Total anthropogenic Solar irradiance #12;Absorbing aerosols: SCIAMACHY Results Outlook #12;SCIAMACHY on ESA's Environmetal Satellite: ENVISAT Polar orbi

  13. Relative humidity and its effect on aerosol optical depth in the vicinity of convective clouds

    E-Print Network [OSTI]

    Altaratz, O

    The hygroscopic growth of aerosols is controlled by the relative humidity (RH) and changes the aerosols' physical and hence optical properties. Observational studies of aerosol–cloud interactions evaluate the aerosol ...

  14. Saharan dust as a causal factor of hemispheric asymmetry in aerosols and cloud cover over the tropical Atlantic Ocean

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Kishcha, Pavel; Da Sliva, Arlindo; Starobinets, Boris; Long, Charles N.; Kalashnikova, Olga; Alpert, Pinhas

    2015-07-09

    Meridional distribution of aerosol optical thickness (AOT) over the tropical Atlantic Ocean (30°N – 30°S) was analyzed to assess seasonal variations of meridional AOT asymmetry. Ten-year MERRA Aerosol Reanalysis (MERRAero) data (July 2002 – June 2012) confirms that the Sahara desert emits a significant amount of dust into the atmosphere over the Atlantic Ocean. Only over the Atlantic Ocean did MERRAero show that desert dust dominates other aerosol species and is responsible for meridional aerosol asymmetry between the tropical North and South Atlantic. Over the 10-year period under consideration, both MISR measurements and MERRAero data showed a pronounced meridional AOTmore »asymmetry. The meridional AOT asymmetry, characterized by the hemispheric ratio (RAOT) of AOT averaged separately over the North and over the South Atlantic, was about 1.7. Seasonally, meridional AOT asymmetry over the Atlantic was the most pronounced between March and July, when dust presence is maximal (RAOT ranged from 2 to 2.4). There was no noticeable meridional aerosol asymmetry in total AOT from September to October. During this period the contribution of carbonaceous aerosols to total AOT in the South Atlantic was comparable to the contribution of dust aerosols to total AOT in the North Atlantic. During the same 10-year period, MODIS cloud fraction (CF) data showed that there was no noticeable asymmetry in meridional CF distribution in different seasons (the hemispheric ratio of CF ranged from 1.0 to 1.2). MODIS CF data illustrated significant cloud cover (CF of 0.7 – 0.9) with limited precipitation ability along the Saharan Air Layer.« less

  15. Aerosol Science and Technology, 45:244261, 2011 Copyright American Association for Aerosol Research

    E-Print Network [OSTI]

    Aerosol Science and Technology, 45:244­261, 2011 Copyright © American Association for Aerosol University, Cambridge, Massachusetts, USA The hygroscopic phase transitions and growth factors of mixed chemical composition on phase transitions. The hygroscopic growth factors of the mixed particles were

  16. Aerosol Science and Technology, 38:12061222, 2004 Copyright c American Association for Aerosol Research

    E-Print Network [OSTI]

    Jimenez, Jose-Luis

    to Combustion-Generated Soot Aerosols as a Function of Fuel Equivalence Ratio Jay G. Slowik,1 K. Stainken,1 Paul factor, size, and fractal dimension of soot aerosol particles generated in a propane/O2 flame were on the fuel equivalence ratio. Type 1: for propane/O2), dva was nearly constant and independent

  17. ARM - Midlatitude Continental Convective Clouds Experiment (MC3E): Multi-Frequency Profilers, 449 MHz Profiler(williams-449_prof)

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Williams, Christopher; Jensen, Mike

    2012-11-06

    This data was collected by the NOAA 449-MHz and 2.8-GHz profilers in support of the Department of Energy (DOE) and NASA sponsored Mid-latitude Continental Convective Cloud Experiment (MC3E). The profiling radars were deployed in Northern Oklahoma at the DOE Atmospheric Radiation Mission (ARM) Southern Great Plans (SGP) Central Facility from 22 April through 6 June 2011. NOAA deployed three instruments: a Parsivel disdrometer, a 2.8-GHz profiler, and a 449-MHz profiler. The parasivel provided surface estimates of the raindrop size distribution and is the reference used to absolutely calibrate the 2.8 GHz profiler. The 2.8-GHz profiler provided unattenuated reflectivity profiles of the precipitation. The 449-MHz profiler provided estimates of the vertical air motion during precipitation from near the surface to just below the freezing level. By using the combination of 2.8-GHz and 449-MHz profiler observations, vertical profiles of raindrop size distributions can be retrieved. The profilers are often reference by their frequency band: the 2.8-GHz profiler operates in the S-band and the 449-MHz profiler operates in the UHF band. The raw observations are available as well as calibrated spectra and moments. This document describes how the instruments were deployed, how the data was collected, and the format of the archived data.

  18. ARM - Midlatitude Continental Convective Clouds Experiment (MC3E): Multi-Frequency Profilers, 449 MHz Profiler(williams-449_prof)

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Williams, Christopher; Jensen, Mike

    This data was collected by the NOAA 449-MHz and 2.8-GHz profilers in support of the Department of Energy (DOE) and NASA sponsored Mid-latitude Continental Convective Cloud Experiment (MC3E). The profiling radars were deployed in Northern Oklahoma at the DOE Atmospheric Radiation Mission (ARM) Southern Great Plans (SGP) Central Facility from 22 April through 6 June 2011. NOAA deployed three instruments: a Parsivel disdrometer, a 2.8-GHz profiler, and a 449-MHz profiler. The parasivel provided surface estimates of the raindrop size distribution and is the reference used to absolutely calibrate the 2.8 GHz profiler. The 2.8-GHz profiler provided unattenuated reflectivity profiles of the precipitation. The 449-MHz profiler provided estimates of the vertical air motion during precipitation from near the surface to just below the freezing level. By using the combination of 2.8-GHz and 449-MHz profiler observations, vertical profiles of raindrop size distributions can be retrieved. The profilers are often reference by their frequency band: the 2.8-GHz profiler operates in the S-band and the 449-MHz profiler operates in the UHF band. The raw observations are available as well as calibrated spectra and moments. This document describes how the instruments were deployed, how the data was collected, and the format of the archived data.

  19. Atmospheric Radiation Measurement Program Science Plan

    SciTech Connect (OSTI)

    Ackerman, T

    2004-10-31

    The Atmospheric Radiation Measurement (ARM) Program has matured into one of the key programs in the U.S. Climate Change Science Program. The ARM Program has achieved considerable scientific success in a broad range of activities, including site and instrument development, atmospheric radiative transfer, aerosol science, determination of cloud properties, cloud modeling, and cloud parameterization testing and development. The focus of ARM science has naturally shifted during the last few years to an increasing emphasis on modeling and parameterization studies to take advantage of the long time series of data now available. During the next 5 years, the principal focus of the ARM science program will be to: Maintain the data record at the fixed ARM sites for at least the next five years. Improve significantly our understanding of and ability to parameterize the 3-D cloud-radiation problem at scales from the local atmospheric column to the global climate model (GCM) grid square. Continue developing techniques to retrieve the properties of all clouds, with a special focus on ice clouds and mixed-phase clouds. Develop a focused research effort on the indirect aerosol problem that spans observations, physical models, and climate model parameterizations. Implement and evaluate an operational methodology to calculate broad-band heating rates in the atmospheric columns at the ARM sites. Develop and implement methodologies to use ARM data more effectively to test atmospheric models, both at the cloud-resolving model scale and the GCM scale. Use these methodologies to diagnose cloud parameterization performance and then refine these parameterizations to improve the accuracy of climate model simulations. In addition, the ARM Program is actively developing a new ARM Mobile Facility (AMF) that will be available for short deployments (several months to a year or more) in climatically important regions. The AMF will have much of the same instrumentation as the remote facilities at ARM's Tropical Western Pacific and the North Slope of Alaska sites. Over time, this new facility will extend ARM science to a much broader range of conditions for model testing.

  20. Atmospheric Transport of Radionuclides

    SciTech Connect (OSTI)

    Crawford, T.V.

    2003-03-03

    The purpose of atmospheric transport and diffusion calculations is to provide estimates of concentration and surface deposition from routine and accidental releases of pollutants to the atmosphere. This paper discusses this topic.

  1. Non-intrusive characterization of heat transfer fluid aerosol formation 

    E-Print Network [OSTI]

    Krishna, Kiran

    2001-01-01

    in process equipment. Predictive models relating the aerosol formation distances, aerosol droplet size, and volume concentrations to bulk liquid pressure, temperature, fluid properties, leak size and ambient conditions are developed. These models will be used...

  2. The seasonality of aerosol properties in Big Bend National Park 

    E-Print Network [OSTI]

    Allen, Christopher Lee

    2007-04-25

    ), to characterize the seasonal variability of the Big Bend regions aerosol optical properties. Mass extinction efficiencies and relative humidity scattering enhancement factors were calculated for both externally and internally mixed aerosol populations for all size...

  3. Apparatus for rapid measurement of aerosol bulk chemical composition

    DOE Patents [OSTI]

    Lee, Yin-Nan E.; Weber, Rodney J.; Orsini, Douglas

    2006-04-18

    An apparatus for continuous on-line measurement of chemical composition of aerosol particles with a fast time resolution is provided. The apparatus includes an enhanced particle size magnifier for producing activated aerosol particles and an enhanced collection device which collects the activated aerosol particles into a liquid stream for quantitative analysis by analytical means. Methods for on-line measurement of chemical composition of aerosol particles are also provided, the method including exposing aerosol carrying sample air to hot saturated steam thereby forming activated aerosol particles; collecting the activated aerosol particles by a collection device for delivery as a jet stream onto an impaction surface; and flushing off the activated aerosol particles from the impaction surface into a liquid stream for delivery of the collected liquid stream to an analytical instrument for quantitative measurement.

  4. Apparatus for rapid measurement of aerosol bulk chemical composition

    DOE Patents [OSTI]

    Lee, Yin-Nan E. (East Setauket, NY); Weber, Rodney J. (Atlanta, GA)

    2003-01-01

    An apparatus and method for continuous on-line measurement of chemical composition of aerosol particles with a fast time resolution are provided. The apparatus includes a modified particle size magnifier for producing activated aerosol particles and a collection device which collects the activated aerosol particles into a liquid stream for quantitative analysis by analytical methods. The method provided for on-line measurement of chemical composition of aerosol particles includes exposing aerosol carrying sample air to hot saturated steam thereby forming activated aerosol particles; collecting the activated aerosol particles by a collection device for delivery as a jet stream onto an impaction surface; flushing off the activated aerosol particles from the impaction surface into a liquid stream for delivery of the collected liquid stream to an analytical instrument for quantitative measurement.

  5. Atmospheric benzenoid emissions from plants rival those from fossil fuels

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Misztal, P. K.; Hewitt, C. N.; Wildt, J.; Blande, J. D.; Eller, A. S.D.; Fares, S.; Gentner, D. R.; Gilman, J. B.; Graus, M.; Greenberg, J.; et al

    2015-07-13

    Despite the known biochemical production of a range of aromatic compounds by plants and the presence of benzenoids in floral scents, the emissions of only a few benzenoid compounds have been reported from the biosphere to the atmosphere. Here, using evidence from measurements at aircraft, ecosystem, tree, branch and leaf scales, with complementary isotopic labeling experiments, we show that vegetation (leaves, flowers, and phytoplankton) emits a wide variety of benzenoid compounds to the atmosphere at substantial rates. Controlled environment experiments show that plants are able to alter their metabolism to produce and release many benzenoids under stress conditions. The functionsmore »of these compounds remain unclear but may be related to chemical communication and protection against stress. We estimate the total global secondary organic aerosol potential from biogenic benzenoids to be similar to that from anthropogenic benzenoids (~10 Tg y-1), pointing to the importance of these natural emissions in atmospheric physics and chemistry.« less

  6. Long-term measurements of submicrometer aerosol chemistry at the Southern Great Plains (SGP) using an Aerosol Chemical Speciation Monitor (ACSM)

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Parworth, Caroline; Tilp, Alison; Fast, Jerome; Mei, Fan; Shippert, Tim; Sivaraman, Chitra; Watson, Thomas; Zhang, Qi

    2015-04-01

    In this study the long-term trends of non-refractory submicrometer aerosol (NR-PM1) composition and mass concentration measured by an Aerosol Chemical Speciation Monitor (ACSM) at the Atmospheric Radiation Measurement (ARM) program's Southern Great Plains (SGP) site are discussed. NR-PM1 data was recorded at ~30 min intervals over a period of 19 months between November 2010 and June 2012. Positive Matrix Factorization (PMF) was performed on the measured organic mass spectral matrix using a rolling window technique to derive factors associated with distinct sources, evolution processes, and physiochemical properties. The rolling window approach also allows us to capture the dynamic variations ofmore »the chemical properties in the organic aerosol (OA) factors over time. Three OA factors were obtained including two oxygenated OA (OOA) factors, differing in degrees of oxidation, and a biomass burning OA (BBOA) factor. Back trajectory analyses were performed to investigate possible sources of major NR-PM1 species at the SGP site. Organics dominated NR-PM1 mass concentration for the majority of the study with the exception of winter, when ammonium nitrate increases due to transport of precursor species from surrounding urban and agricultural areas and also due to cooler temperatures. Sulfate mass concentrations have little seasonal variation with mixed regional and local sources. In the spring BBOA emissions increase and are mainly associated with local fires. Isoprene and carbon monoxide emission rates were obtained by the Model of Emissions of Gases and Aerosols from Nature (MEGAN) and the 2011 U.S. National Emissions Inventory to represent the spatial distribution of biogenic and anthropogenic sources, respectively. The combined spatial distribution of isoprene emissions and air mass trajectories suggest that biogenic emissions from the southeast contribute to SOA formation at the SGP site during the summer.« less

  7. Atmospheric chemistry and global change

    E-Print Network [OSTI]

    Prather, MJ

    1999-01-01

    and particles. Thus Atmospheric Chemistry and Global Changethe future of atmospheric chemistry. BROWSINGS Tornadothe complexity of atmospheric chemistry well, but trips a

  8. Multiday production of condensing organic aerosol mass in urban and forest outflow

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Lee-Taylor, J.; Hodzic, A.; Madronich, S.; Aumont, B.; Camredon, M.; Valorso, R.

    2015-01-16

    Secondary organic aerosol (SOA) production in air masses containing either anthropogenic or biogenic (terpene-dominated) emissions is investigated using the explicit gas-phase chemical mechanism generator GECKO-A. Simulations show several-fold increases in SOA mass continuing for multiple days in the urban outflow, even as the initial air parcel is diluted into the regional atmosphere. The SOA mass increase in the forest outflow is more modest (~50%) and of shorter duration (1–2 days). The multiday production in the urban outflow stems from continuing oxidation of gas-phase precursors which persist in equilibrium with the particle phase, and can be attributed to multigenerational reaction productsmore »of both aromatics and alkanes, especially those with relatively low carbon numbers (C4–15). In particular we find large contributions from substituted maleic anhydrides and multi-substituted peroxide-bicyclic alkenes. The results show that the predicted production is a robust feature of our model even under changing atmospheric conditions and different vapor pressure schemes, and contradict the notion that SOA undergoes little mass production beyond a short initial formation period. The results imply that anthropogenic aerosol precursors could influence the chemical and radiative characteristics of the atmosphere over an extremely wide region, and that SOA measurements near precursor sources may routinely underestimate this influence.« less

  9. Multiday production of condensing organic aerosol mass in urban and forest outflow

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Lee-Taylor, J.; Hodzic, A.; Madronich, S.; Aumont, B.; Camredon, M.; Valorso, R.

    2014-07-03

    Secondary organic aerosol (SOA) production in air masses containing either anthropogenic or biogenic (terpene-dominated) emissions is investigated using the explicit gas-phase chemical mechanism generator GECKO-A. Simulations show several-fold increases in SOA mass continuing for several days in the urban outflow, even as the initial air parcel is diluted into the regional atmosphere. The SOA mass increase in the forest outflow is more modest (?50%) and of shorter duration (1–2 days). The production in the urban outflow stems from continuing oxidation of gas-phase precursors which persist in equilibrium with the particle phase, and can be attributed to multigenerational reaction products ofmore »both aromatics and alkanes. In particular we find large contributions from substituted maleic anhydrides and multi-substituted peroxide-bicyclic alkenes. The results show that the predicted production is a robust feature of our model even under changing atmospheric conditions, and contradict the notion that SOA undergoes little mass production beyond a short initial formation period. The results imply that anthropogenic aerosol precursors could influence the chemical and radiative characteristics of the atmosphere over an extremely wide region, and that SOA measurements near precursor sources may routinely underestimate this influence.« less

  10. New Atmospheric Profiling Instrument Added to SGP CART Suite

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration wouldMass map shinesSolar Photovoltaic(MillionNatureThousand Cubic Feet) Sold3 New

  11. Effect of Aerosol Humidification on the Column Aerosol Optical Thickness

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration would like submitKansas Nuclear Profile 2010MesoscopyStaff »Vehicle automation is aover the ARM

  12. ARM - Midlatitude Continental Convective Clouds - Ultra High Sensitivity Aerosol Spectrometer(tomlinson-uhsas)

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Tomlinson, Jason; Jensen, Mike

    Ultra High Sensitivity Aerosol Spectrometer (UHSASA) A major component of the Mid-latitude Continental Convective Clouds Experiment (MC3E) field campaign was the deployment of an enhanced radiosonde array designed to capture the vertical profile of atmospheric state variables (pressure, temperature, humidity wind speed and wind direction) for the purpose of deriving the large-scale forcing for use in modeling studies. The radiosonde array included six sites (enhanced Central Facility [CF-1] plus five new sites) launching radiosondes at 3-6 hour sampling intervals. The network will cover an area of approximately (300)2 km2 with five outer sounding launch sites and one central launch location. The five outer sounding launch sites are: S01 Pratt, KS [ 37.7oN, 98.75oW]; S02 Chanute, KS [37.674, 95.488]; S03 Vici, Oklahoma [36.071, -99.204]; S04 Morris, Oklahoma [35.687, -95.856]; and S05 Purcell, Oklahoma [34.985, -97.522]. Soundings from the SGP Central Facility during MC3E can be retrieved from the regular ARM archive. During routine MC3E operations 4 radiosondes were launched from each of these sites (approx. 0130, 0730, 1330 and 1930 UTC). On days that were forecast to be convective up to four additional launches were launched at each site (approx. 0430, 1030, 1630, 2230 UTC). There were a total of approximately 14 of these high frequency launch days over the course of the experiment. These files contain brightness temperatures observed at Purcell during MC3E. The measurements were made with a 5 channel (22.235, 23.035, 23.835, 26.235, 30.000GHz) microwave radiometer at one minute intervals. The results have been separated into daily files and the day of observations is indicated in the file name. All observations were zenith pointing. Included in the files are the time variables base_time and time_offset. These follow the ARM time conventions. Base_time is the number seconds since January 1, 1970 at 00:00:00 for the first data point of the file and time_offset is the offset in seconds from base_time.

  13. ARM - Midlatitude Continental Convective Clouds - Ultra High Sensitivity Aerosol Spectrometer(tomlinson-uhsas)

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Tomlinson, Jason; Jensen, Mike

    2012-02-28

    Ultra High Sensitivity Aerosol Spectrometer (UHSASA) A major component of the Mid-latitude Continental Convective Clouds Experiment (MC3E) field campaign was the deployment of an enhanced radiosonde array designed to capture the vertical profile of atmospheric state variables (pressure, temperature, humidity wind speed and wind direction) for the purpose of deriving the large-scale forcing for use in modeling studies. The radiosonde array included six sites (enhanced Central Facility [CF-1] plus five new sites) launching radiosondes at 3-6 hour sampling intervals. The network will cover an area of approximately (300)2 km2 with five outer sounding launch sites and one central launch location. The five outer sounding launch sites are: S01 Pratt, KS [ 37.7oN, 98.75oW]; S02 Chanute, KS [37.674, 95.488]; S03 Vici, Oklahoma [36.071, -99.204]; S04 Morris, Oklahoma [35.687, -95.856]; and S05 Purcell, Oklahoma [34.985, -97.522]. Soundings from the SGP Central Facility during MC3E can be retrieved from the regular ARM archive. During routine MC3E operations 4 radiosondes were launched from each of these sites (approx. 0130, 0730, 1330 and 1930 UTC). On days that were forecast to be convective up to four additional launches were launched at each site (approx. 0430, 1030, 1630, 2230 UTC). There were a total of approximately 14 of these high frequency launch days over the course of the experiment. These files contain brightness temperatures observed at Purcell during MC3E. The measurements were made with a 5 channel (22.235, 23.035, 23.835, 26.235, 30.000GHz) microwave radiometer at one minute intervals. The results have been separated into daily files and the day of observations is indicated in the file name. All observations were zenith pointing. Included in the files are the time variables base_time and time_offset. These follow the ARM time conventions. Base_time is the number seconds since January 1, 1970 at 00:00:00 for the first data point of the file and time_offset is the offset in seconds from base_time.

  14. Atmospheric lead in downtown Guatemala City

    SciTech Connect (OSTI)

    Durando, M.L.; Aragon, S.R.

    1982-01-01

    Atomic absorption (AA) analysis was employed to determine, for the first time in this country, lead concentrations in aerosols collected in Nuclepore filter media during the months of February and March (1980) in Guatemala City, Guatemala. In particular, the lead in the atmospheric fine particulate was measured in different downtown locations around noontime and in a single location at 1-h intervals throughout the day. The first was used to study short-term variations from one location to the other, and the second one was used to correlate parameters such as traffic density and wind velocity with the levels of airborne lead on the same day. In addition, this paper presents a brief discussion of the lead content in Guatemalan gasoline, the lead levels in street dusts, and the total suspended particulate matter in downtown Guatemala City.

  15. The Radiative Role of Free Tropospheric Aerosols and Marine Clouds over the Central North Atlantic

    SciTech Connect (OSTI)

    Mazzoleni, Claudio; Kumar, Sumit; Wright, Kendra; Kramer, Louisa; Mazzoleni, Lynn; Owen, Robert; Helmig, Detlev

    2014-12-09

    The scientific scope of the project was to exploit the unique location of the Pico Mountain Observatory (PMO) located in the summit caldera of the Pico Volcano in Pico Island in the Azores, for atmospheric studies. The observatory, located at 2225m a.s.l., typically samples free tropospheric aerosols laying above the marine low-level clouds and long-range transported from North America. The broad purpose of this research was to provide the scientific community with a better understanding of fundamental physical processes governing the effects of aerosols on radiative forcing and climate; with the ultimate goal of improving our abilities to understand past climate and to predict future changes through numerical models. The project was 'exploratory' in nature, with the plan to demonstrate the feasibility of deploying for the first time, an extensive aerosol research package at PMO. One of the primary activities was to test the deployment of these instruments at the site, to collect data during the 2012 summer season, and to further develop the infrastructure and the knowledge for performing novel research at PMO in follow-up longer-term aerosol-cloud studies. In the future, PMO could provide an elevated research outpost to support the renewed DOE effort in the Azores that was intensified in 2013 with the opening of the new sea-level ARM-DOE Eastern North Atlantic permanent facility at Graciosa Island. During the project period, extensive new data sets were collected for the planned 2012 season. Thanks to other synergistic activities and opportunities, data collection was then successfully extended to 2013 and 2014. Highlights of the scientific findings during this project include: a) biomass burning contribute significantly to the aerosol loading in the North Atlantic free troposphere; however, long-range transported black carbon concentrations decreased substantially in the last decade. b) Single black carbon particles – analyzed off-line at the electron microscope – were often very compacted, suggesting cloud processing and exhibiting different optical properties from fresh emissions. In addition, black carbon was found to be sometimes mixed with mineral dust, affecting its optical properties and potential forcing. c) Some aerosols collected at PMO acted as ice nuclei, potentially contributing to cirrus cloud formation during their transport in the upper free troposphere. Identified good ice nuclei were often mineral dust particles. d) The free tropospheric aerosols studied at PMO have relevance to low level marine clouds due, for example, to synoptic subsidence entraining free tropospheric aerosols into the marine boundary layer. This has potentially large consequences on cloud condensation nuclei concentrations and compositions in the marine boundary layer; therefore, having an effect on the marine stratus clouds, with potentially important repercussions on the radiative forcing. The scientific products of this project currently include contributions to two papers published in the Nature Publishing group (Nature Communications and Scientific Reports), one paper under revision for Atmospheric Chemistry and Physics, one in review in Geophysical Research Letters and one recently submitted to Atmospheric Chemistry and Physics Discussion. In addition, four manuscripts are in advanced state of preparation. Finally, twenty-eight presentations were given at international conferences, workshops and seminars.

  16. AEROSOL-PRECIPITATION INTERACTIONS IN THE SOUTHERN APPALACHIAN MOUNTAINS

    E-Print Network [OSTI]

    AEROSOL-PRECIPITATION INTERACTIONS IN THE SOUTHERN APPALACHIAN MOUNTAINS A Thesis by GINGER MARIE of the requirements for the degree of MASTER OF ARTS May 2011 Department of Geography and Planning #12;AEROSOL-PRECIPITATION and Graduate Studies #12;Copyright by Ginger Marie Kelly 2011 All Rights Reserved #12;iv ABSTRACT AEROSOL-PRECIPITATION

  17. Aerodynamic Focusing Of High-Density Aerosols

    SciTech Connect (OSTI)

    Ruiz, D. E.; Fisch, Nathaniel

    2014-02-24

    High-density micron-sized particle aerosols might form the basis for a number of applications in which a material target with a particular shape might be quickly ionized to form a cylindrical or sheet shaped plasma. A simple experimental device was built in order to study the properties of high-density aerosol focusing for 1#22; m silica spheres. Preliminary results recover previous findings on aerodynamic focusing at low densities. At higher densities, it is demonstrated that the focusing properties change in a way which is consistent with a density dependent Stokes number.

  18. Flattening coefficient of aerosols collected on treated slides 

    E-Print Network [OSTI]

    Olan-Figueroa, Excel

    1981-01-01

    was found to be 1. 338, and for DOP, 1. 354. There is no apparent variation of F with particle diameter for aerosols in the 2. 7-29. 1 um range. The slightly lower value of F for oleic acid suggests that the contact angle of oleic acid with respect... monodisoerse aerosols in the 1. 5 to 50 um diameter range, the vibratino j et monodisperse aerosol generator has been used. The monodisperse aerosols generated by this device can be considered as an "aerosol standard" since the size and concentration...

  19. Near real time vapor detection and enhancement using aerosol adsorption

    DOE Patents [OSTI]

    Novick, V.J.; Johnson, S.A.

    1999-08-03

    A vapor sample detection method is described where the vapor sample contains vapor and ambient air and surrounding natural background particles. The vapor sample detection method includes the steps of generating a supply of aerosol that have a particular effective median particle size, mixing the aerosol with the vapor sample forming aerosol and adsorbed vapor suspended in an air stream, impacting the suspended aerosol and adsorbed vapor upon a reflecting element, alternatively directing infrared light to the impacted aerosol and adsorbed vapor, detecting and analyzing the alternatively directed infrared light in essentially real time using a spectrometer and a microcomputer and identifying the vapor sample. 13 figs.

  20. Global and regional modeling of clouds and aerosols in the marine boundary layer during VOCALS: the VOCA intercomparison

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Wyant, M. C.; Bretherton, Christopher S.; Wood, Robert; Carmichael, Gregory; Clarke, A. D.; Fast, Jerome D.; George, R.; Gustafson, William I.; Hannay, Cecile; Lauer, Axel; et al

    2015-01-09

    A diverse collection of models are used to simulate the marine boundary layer in the southeast Pacific region during the period of the October–November 2008 VOCALS REx (VAMOS Ocean Cloud Atmosphere Land Study Regional Experiment) field campaign. Regional models simulate the period continuously in boundary-forced free-running mode, while global forecast models and GCMs (general circulation models) are run in forecast mode. The models are compared to extensive observations along a line at 20° S extending westward from the South American coast. Most of the models simulate cloud and aerosol characteristics and gradients across the region that are recognizably similar tomore »observations, despite the complex interaction of processes involved in the problem, many of which are parameterized or poorly resolved. Some models simulate the regional low cloud cover well, though many models underestimate MBL (marine boundary layer) depth near the coast. Most models qualitatively simulate the observed offshore gradients of SO2, sulfate aerosol, CCN (cloud condensation nuclei) concentration in the MBL as well as differences in concentration between the MBL and the free troposphere. Most models also qualitatively capture the decrease in cloud droplet number away from the coast. However, there are large quantitative intermodel differences in both means and gradients of these quantities. Many models are able to represent episodic offshore increases in cloud droplet number and aerosol concentrations associated with periods of offshore flow. Most models underestimate CCN (at 0.1% supersaturation) in the MBL and free troposphere. The GCMs also have difficulty simulating coastal gradients in CCN and cloud droplet number concentration near the coast. The overall performance of the models demonstrates their potential utility in simulating aerosol–cloud interactions in the MBL, though quantitative estimation of aerosol–cloud interactions and aerosol indirect effects of MBL clouds with these models remains uncertain.« less

  1. Global and regional modeling of clouds and aerosols in the marine boundary layer during VOCALS: the VOCA intercomparison

    SciTech Connect (OSTI)

    Wyant, M. C.; Bretherton, Christopher S.; Wood, Robert; Carmichael, Gregory; Clarke, A. D.; Fast, Jerome D.; George, R.; Gustafson, William I.; Hannay, Cecile; Lauer, Axel; Lin, Yanluan; Morcrette, J. -J.; Mulcahay, Jane; Saide, Pablo; Spak, S. N.; Yang, Qing

    2015-01-01

    A diverse collection of models are used to simulate the marine boundary layer in the southeast Pacific region during the period of the October–November 2008 VOCALS REx (VAMOS Ocean Cloud Atmosphere Land Study Regional Experiment) field campaign. Regional models simulate the period continuously in boundary-forced free-running mode, while global forecast models and GCMs (general circulation models) are run in forecast mode. The models are compared to extensive observations along a line at 20° S extending westward from the South American coast. Most of the models simulate cloud and aerosol characteristics and gradients across the region that are recognizably similar to observations, despite the complex interaction of processes involved in the problem, many of which are parameterized or poorly resolved. Some models simulate the regional low cloud cover well, though many models underestimate MBL (marine boundary layer) depth near the coast. Most models qualitatively simulate the observed offshore gradients of SO2, sulfate aerosol, CCN (cloud condensation nuclei) concentration in the MBL as well as differences in concentration between the MBL and the free troposphere. Most models also qualitatively capture the decrease in cloud droplet number away from the coast. However, there are large quantitative intermodel differences in both means and gradients of these quantities. Many models are able to represent episodic offshore increases in cloud droplet number and aerosol concentrations associated with periods of offshore flow. Most models underestimate CCN (at 0.1% supersaturation) in the MBL and free troposphere. The GCMs also have difficulty simulating coastal gradients in CCN and cloud droplet number concentration near the coast. The overall performance of the models demonstrates their potential utility in simulating aerosol–cloud interactions in the MBL, though quantitative estimation of aerosol–cloud interactions and aerosol indirect effects of MBL clouds with these models remains uncertain.

  2. Organic aerosol components observed in Northern Hemispheric datasets from Aerosol Mass Spectrometry

    E-Print Network [OSTI]

    Kroll, Jesse

    In this study we compile and present results from the factor analysis of 43 Aerosol Mass Spectrometer (AMS) datasets (27 of the datasets are reanalyzed in this work). The components from all sites, when taken together, ...

  3. Effect of Hydrophobic Primary Organic Aerosols on Secondary Organic Aerosol Formation from Ozonolysis of ?-Pinene

    SciTech Connect (OSTI)

    Song, Chen; Zaveri, Rahul A.; Alexander, M. Lizabeth; Thornton, Joel A.; Madronich, Sasha; Ortega, John V.; Zelenyuk, Alla; Yu, Xiao-Ying; Laskin, Alexander; Maughan, A. D.

    2007-10-16

    Semi-empirical secondary organic aerosol (SOA) models typically assume a well-mixed organic aerosol phase even in the presence of hydrophobic primary organic aerosols (POA). This assumption significantly enhances the modeled SOA yields as additional organic mass is made available to absorb greater amounts of oxidized secondary organic gases than otherwise. We investigate the applicability of this critical assumption by measuring SOA yields from ozonolysis of ?-pinene (a major biogenic SOA precursor) in a smog chamber in the absence and in the presence of dioctyl phthalate (DOP) and lubricating oil seed aerosol. These particles serve as surrogates for urban hydrophobic POA. The results show that these POA did not enhance the SOA yields. If these results are found to apply to other biogenic SOA precursors, then the semi-empirical models used in many global models would predict significantly less biogenic SOA mass and display reduced sensitivity to anthropogenic POA emissions than previously thought.

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

    SciTech Connect (OSTI)

    Smith, Steven J.; Bond, Tami C.

    2014-01-20

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

  5. Transboundary Secondary Organic Aerosol in Western Japan: An Observed Limitation of the f44 Oxidation Indicator

    E-Print Network [OSTI]

    Irei, Satoshi; Sadanaga, Yasuhiro; Miyoshi, Takao; Arakaki, Tekemitsu; Sato, Kei; Kaneyasu, Naoki; Bandow, Hiroshi; Hatakeyama, Shiro

    2015-01-01

    To obtain evidence for secondary organic aerosol formation during the long range transport of air masses over the East China Sea, we conducted field measurements in March 2012 at the Fukue atmospheric monitoring station, Nagasaki, in western Japan. The relative abundance of m/z 44 in fine organic aerosol mass spectra (f44) was measured by an Aerodyne aerosol chemical speciation monitor. The stable carbon isotope ratio (d13C) of low volatile water soluble organic carbon (LV-WSOC) in the daily filter samples of total suspended particulate matter was also analyzed using an elemental analyzer coupled with an isotope ratio mass spectrometer. Additionally, in situ measurements of NOx and NOy were performed using NOx and NOy analyzers. The measurements showed that, unlike the systematic trends observed in a previous field study, a scatter plot for d13C of LV-WSOC versus f44 indicated a random variation. Comparison of f44 with the photochemical age estimated by the NOx to NOy ratio revealed that the f44 values distri...

  6. Results from simulated upper-plenum aerosol transport and aerosol resuspension experiments

    SciTech Connect (OSTI)

    Wright, A.L.; Pattison, W.L.

    1984-01-01

    Recent calculational results published as part of the Battelle-Columbus BMI-2104 source term study indicate that, for some LWR accident sequences, aerosol deposition in the reactor primary coolant system (PCS) can lead to significant reductions in the radionuclide source term. Aerosol transport and deposition in the PCS have been calculated in this study using the TRAP-MELT 2 computer code, which was developed at Battelle-Columbus; the status of validation of the TRAP-MELT 2 code has been described in an Oak Ridge National Laboratory (ORNL) report. The objective of the ORNL TRAP-MELT Validation Project, which is sponsored by the Fuel Systems Behavior Research Branch of the US Nuclear Regulatory Commission, is to conduct simulated reactor-vessel upper-plenum aerosol deposition and transport tests. The results from these tests will be used in the ongoing effort to validate TRAP-MELT 2. The TRAP-MELT Validation Project includes two experimental subtasks. In the Aerosol Transport Tests, aerosol transport in a vertical pipe is being studied; this geometry was chosen to simulate aerosol deposition and transport in the reactor-vessel upper-plenum. To date, four experiments have been performed; the results from these tests are presented in this paper. 7 refs., 4 figs., 4 tabs.

  7. Single point aerosol sampling: Evaluation of mixing and probe performance in a nuclear stack

    SciTech Connect (OSTI)

    Rodgers, J.C.; Fairchild, C.I.; Wood, G.O.; Ortiz, C.A.; Muyshondt, A.; McFarland, A.R. |

    1994-12-31

    Alternative Reference Methodologies (ARMS) have been developed for sampling of radionuclide; from stacks and ducts that differ from the methods required by the US EPA. The EPA methods are prescriptive in selection of sampling locations and in design of sampling probes whereas the alternative methods are performance driven. Tests were conducted in a stack at Los Alamos National Laboratory to demonstrate the efficacy of the ARMS. Coefficients of variation of the velocity tracer gas, and aerosol particle profiles were determined at three sampling locations. Results showed numerical criteria placed upon the coefficients of variation by the ARMs were met at sampling stations located 9 and 14 stack diameters from flow entrance, but not at a location that is 1.5 diameters downstream from the inlet. Experiments were conducted to characterize the transmission of 10 {mu}m aerodynamic equivalent diameter liquid aerosol particles through three types of sampling probes. The transmission ratio (ratio of aerosol concentration at the probe exit plane to the concentration in the free stream) was 107% for a 113 L/min (4-cfm) an isokinetic shrouded probe, but only 20% for an isokinetic probe that follows the EPA requirements. A specially designed isokinetic probe showed a transmission ratio of 63%. The shrouded probe performance would conform to the ARM criteria; however, the isokinetic probes would not.

  8. Experimental study of nuclear workplace aerosol samplers 

    E-Print Network [OSTI]

    Parulian, Antony

    1995-01-01

    consists of an inlet-elbow, a transport line, and a EL-900 CAM prototype manufactured by EG&G. Results show that only 12% of 10 []m aerodynamic diameter (AD) aerosol particles penetrate through the complete sampling system when it is operated at flow rate...

  9. Atmospheric Neutrino Fluxes

    E-Print Network [OSTI]

    Thomas K. Gaisser

    2005-02-18

    Starting with an historical review, I summarize the status of calculations of the flux of atmospheric neutrinos and how they compare to measurements.

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

    SciTech Connect (OSTI)

    Meskhidze, Nicholas; Zhang, Yang; Kamykowski, Daniel

    2012-03-28

    In this DOE project the improvements to parameterization of marine primary organic matter (POM) emissions, hygroscopic properties of marine POM, marine isoprene derived secondary organic aerosol (SOA) emissions, surfactant effects, new cloud droplet activation parameterization have been implemented into Community Atmosphere Model (CAM 5.0), with a seven mode aerosol module from the Pacific Northwest National Laboratory (PNNL)���¢��������s Modal Aerosol Model (MAM7). The effects of marine aerosols derived from sea spray and ocean emitted biogenic volatile organic compounds (BVOCs) on microphysical properties of clouds were explored by conducting 10 year CAM5.0-MAM7 model simulations at a grid resolution 1.9�������°��������2.5�������° with 30 vertical layers. Model-predicted relationship between ocean physical and biological systems and the abundance of CCN in remote marine atmosphere was compared to data from the A-Train satellites (MODIS, CALIPSO, AMSR-E). Model simulations show that on average, primary and secondary organic aerosol emissions from the ocean can yield up to 20% increase in Cloud Condensation Nuclei (CCN) at 0.2% Supersaturation, and up to 5% increases in droplet number concentration of global maritime shallow clouds. Marine organics were treated as internally or externally mixed with sea salt. Changes associated with cloud properties reduced (absolute value) the model-predicted short wave cloud forcing from -1.35 Wm-2 to -0.25 Wm-2. By using different emission scenarios, and droplet activation parameterizations, this study suggests that addition of marine primary aerosols and biologically generated reactive gases makes an important difference in radiative forcing assessments. All baseline and sensitivity simulations for 2001 and 2050 using global-through-urban WRF/Chem (GU-WRF) were completed. The main objective of these simulations was to evaluate the capability of GU-WRF for an accurate representation of the global atmosphere by exploring the most accurate configuration of physics options in GWRF for global scale modeling in 2001 at a horizontal grid resolution of 1�������° x 1�������°. GU-WRF model output was evaluated using observational datasets from a variety of sources including surface based observations (NCDC and BSRN), model reanalysis (NCEP/ NCAR Reanalysis and CMAP), and remotely-sensed data (TRMM) to evaluate the ability of GU-WRF to simulate atmospheric variables at the surface as well as aloft. Explicit treatment of nanoparticles produced from new particle formation in GU-WRF/Chem-MADRID was achieved by expanding particle size sections from 8 to 12 to cover particles with the size range of 1.16 nm to 11.6 �������µm. Simulations with two different nucleation parameterizations were conducted for August 2002 over a global domain at a 4�������º by 5�������º horizontal resolution. The results are evaluated against field measurement data from the 2002 Aerosol Nucleation and Real Time Characterization Experiment (ANARChE) in Atlanta, Georgia, as well as satellite and reanalysis data. We have also explored the relationship between ���¢��������clean marine���¢������� aerosol optical properties and ocean surface wind speed using remotely sensed data from the Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP) on board the CALIPSO satellite and the Advanced Microwave Scanning Radiometer (AMSR-E) on board the AQUA satellite. Detailed data analyses

  11. Evaluation of Preindustrial to Present-day Black Carbon and its Albedo Forcing from Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP)

    SciTech Connect (OSTI)

    Lee, Y. H.; Lamarque, J.-F.; Flanner, M. G.; Jiao, C.; Shindell, Drew; Berntsen, T.; Bisiauxs, M.; Cao, J.; Collins, W. J.; Curran, M.; Edwards, R.; Faluvegi, G.; Ghan, Steven J.; Horowitz, L.; McConnell, J.R.; Ming, J.; Myhre, G.; Nagashima, T.; Naik, Vaishali; Rumbold, S.; Skeie, R. B.; Sudo, K.; Takemura, T.; Thevenon, F.; Xu, B.; Yoon, Jin-Ho

    2013-03-05

    As a part of the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP), we evaluate the historical black carbon (BC) aerosols simulated by 8 ACCMIP models against the observations including 12 ice core records, a long-term surface mass concentrations and recent Arctic BC snowpack measurements. We also estimate BC albedo forcing by performing additional simulations using the NCAR Community Land and Sea-Ice model 4 with prescribed meteorology from 1996-2000, which includes the SNICAR BC-snow model. We evaluated the vertical profile of BC snow concentrations from these offline simulations to using recent BC snowpack measurements. Despite using the same BC emissions, global BC burden differs by approximately a factor of 3 among models due to the differences in aerosol removal parameterizations and simulated meteorology among models; 34 Gg to 103 Gg in 1850 and 82 Gg to 315 Gg in 2000. However,models agree well on 2.5~3 times increase in the global BC burden from preindustrial to present-day, which matches with the 2.5 times increase in BC emissions. We find a large model diversity at both NH and SH high latitude regions for BC burden and at SH high latitude regions for deposition fluxes. The ACCMIP simulations match the observed BC mass concentrations well in Europe and North America except at Jungfrauch and Ispra. However, the models fail to capture the Arctic BC seasonality due tosevere underestimations during winter and spring. Compared to recent snowpack measurements, the simulated vertically resolved BC snow concentrations are, on average, within a factor of 2-3 of observations except for Greenland and Arctic Ocean. However, model and observation differ widely due to missing interannual variations in emissions and possibly due to the choice of the prescribed meteorology period (i.e., 1996-2000).

  12. Plutonium-aerosol emission rates and human pulmonary deposition calculations for Nuclear Site 201, Nevada Test Site

    SciTech Connect (OSTI)

    Shinn, J.H.; Homan, D.N.

    1982-06-21

    This study determined the plutonium-aerosol fluxes from the soil to quantify (1) the extent of potential human exposure by deep-lung retention of alpha-emitting particles; (2) the source term should there be any significant, long-term, transport of plutonium aerosols; and (3) the resuspension factor and rate so that, for the first time at any nuclear site, one may calculate how long it will take for wind erosion to carry away a significant amount of the contaminated soil. High-volume air samplers and cascade impactors were used to characterize the plutonium aerosols. Meteorological flux-profile methods were used to calculate dust and plutonium aerosol emission rates. A floorless wind tunnel (10-m long) was used to examine resuspension under steady-state, high wind speed. The resuspension factor was two orders of magnitude lower than the other comparable sites at NTS and elsewhere, and the average resuspension rate of 5.3 x 10/sup -8//d was also very low, so that the half-time for resuspension by wind erosion was about 36,000 y.

  13. Oceanography and Atmospheric Sciences

    E-Print Network [OSTI]

    Kurapov, Alexander

    Oceanography and Atmospheric Sciences 1959­2009 WayneBurt. #12;Oceanography and Atmospheric in Oceanography (TENOC). Wayne Burt immediately responds with proposal to President Strand of Oregon State College to start a graduate Department of Oceanography. 1959 Oregon State Board of Higher Education approves

  14. Intercomparison and Evaluation of Global Aerosol Microphysical Properties among AeroCom Models of a Range of Complexity

    SciTech Connect (OSTI)

    Mann, G. W.; Carslaw, K. S.; Reddington, C. L.; Pringle, K. J.; Schulz, M.; Asmi, A.; Spracklen, D. V.; Ridley, D. A.; Woodhouse, M. T.; Lee, L. A.; Zhang, Kai; Ghan, Steven J.; Easter, Richard C.; Liu, Xiaohong; Stier, P.; Lee, Y. H.; Adams, P. J.; Tost, H.; Lelieveld, J.; Bauer, S.; Tsigaridis, Kostas; van Noije, T.; Strunk, A.; Vignati, E.; Bellouin, N.; Dalvi, M.; Johnson, C. E.; Bergman, T.; Kokkola, H.; Von Salzen, Knut; Yu, Fangqun; Luo, Gan; Petzold, A.; Heintzenberg, J.; Clarke, A. D.; Ogren, J. A.; Gras, J.; Baltensperger, Urs; Kaminski, U.; Jennings, S. G.; O'Dowd, C. D.; Harrison, R. M.; Beddows, D. C.; Kulmala, M.; Viisanen, Y.; Ulevicius, V.; Mihalopoulos, Nikos; Zdimal, V.; Fiebig, M.; Hansson, H. C.; Swietlicki, E.; Henzing, J. S.

    2014-05-13

    Many of the next generation of global climate models will include aerosol schemes which explicitly simulate the microphysical processes that determine the particle size distribution. These models enable aerosol optical properties and cloud condensation nuclei (CCN) concentrations to be determined by fundamental aerosol processes, which should lead to a more physically based simulation of aerosol direct and indirect radiative forcings. This study examines the global variation in particle size distribution simulated by twelve global aerosol microphysics models to quantify model diversity and to identify any common biases against observations. Evaluation against size distribution measurements from a new European network of aerosol supersites shows that the mean model agrees quite well with the observations at many sites on the annual mean, but there are some seasonal biases common to many sites. In particular, at many of these European sites, the accumulation mode number concentration is biased low during winter and Aitken mode concentrations tend to be overestimated in winter and underestimated in summer. At high northern latitudes, the models strongly underpredict Aitken and accumulation particle concentrations compared to the measurements, consistent with previous studies that have highlighted the poor performance of global aerosol models in the Arctic. In the marine boundary layer, the models capture the observed meridional variation in the size distribution, which is dominated by the Aitken mode at high latitudes, with an increasing concentration of accumulation particles with decreasing latitude. Considering vertical profiles, the models reproduce the observed peak in total particle concentrations in the upper troposphere due to new particle formation, although modelled peak concentrations tend to be biased high over Europe. Overall, the results suggest that most global aerosol microphysics models simulate the global variation of the particle size distribution with a good degree of skill, but some models are in poor agreement with the observations. Further work is required to better constrain size-resolved primary and secondary particle number sources, and an improved understanding of nucleation and growth (e.g. the role of nitrate and secondary organics) will improve the fidelity of simulated particle size distributions.

  15. Gaseous Chemistry and Aerosol Mechanism Developments for Version 3.5.1 of the Online Regional Model, WRF-Chem

    SciTech Connect (OSTI)

    Archer-Nicholls, Scott; Lowe, Douglas; Utembe, Steve; Allan, James D.; Zaveri, Rahul A.; Fast, Jerome D.; Hodnebrog, Oivind; Denier van der Gon, Hugo; McFiggans, Gordon

    2014-11-08

    We have made a number of developments in the regional coupled model WRF-Chem, with the aim of making the model more suitable for prediction of atmospheric composition and of interactions between air quality and weather. We have worked on the European domain, with a particular focus on making the model suitable for the study of night time chemistry and oxidation by the nitrate radical in the UK atmosphere. A reduced form of the Common Reactive Intermediates gas-phase chemical mechanism (CRIv2-R5) has been implemented to enable more explicit simulation of VOC degradation. N2O5 heterogeneous chemistry has been added to the existing sectional MOSAIC aerosol module, and coupled to both the CRIv2-R5 and existing CBM-Z gas phase scheme. Modifications have also been made to the sea-spray aerosol emission representation, allowing the inclusion of primary organic material in sea-spray aerosol. Driven by appropriate emissions, wind fields and chemical boundary conditions, implementation of the different developments is illustrated in order to demonstrate the impact that these changes have in the North-West European domain. These developments are now part of the freely available WRF-Chem distribution.

  16. Aerosol optical hygroscopicity measurements during the 2010 CARES Campaign

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Atkinson, D. B.; Radney, J. G.; Lum, J.; Kolesar, K. R.; Cziczo, D. J.; Pekour, M. S.; Zhang, Q.; Setyan, A.; Zelenyuk, A.; Cappa, C. D.

    2014-12-10

    Measurements of the effect of water uptake on particulate light extinction or scattering made at two locations during the 2010 CARES study around Sacramento, CA are reported. The observed influence of water uptake, characterized through the dimensionless optical hygroscopicity parameter ?, is compared with calculations constrained by observed particle size distributions and size-dependent particle composition. A closure assessment has been carried out that allowed for determination of the average hygroscopic growth factors (GF) at 85% relative humidity and the dimensionless hygroscopicity parameter ? for oxygenated organic aerosol (OA) and for supermicron particles, yielding ? = 0.1–0.15 and 0.9–1.0, respectively. Themore »derived range of oxygenated OA ? values are in line with previous observations. The relatively large values for supermicron particles is consistent with substantial contributions of sea salt-containing particles in this size range. Analysis of time-dependent variations in the supermicron particle hygroscopicity suggest that atmospheric processing, specifically chloride displacement by nitrate and the accumulation of secondary organics on supermicron particles, can lead to substantial depression of the observed GF.« less

  17. Aerosol optical hygroscopicity measurements during the 2010 CARES Campaign

    SciTech Connect (OSTI)

    Atkinson, D. B.; Radney, J. G.; Lum, J.; Kolesar, K. R.; Cziczo, Daniel J.; Pekour, Mikhail S.; Zhang, Qi; Setyan, Ari; Zelenyuk, Alla; Cappa, Christopher

    2015-01-01

    Measurements of the effect of water uptake on particulate light extinction or scattering made at two locations during the 2010 CARES study around Sacramento, CA are reported. The observed influence of water uptake, characterized through the dimensionless optical hygroscopicity parameter ?, is compared with calculations constrained by observed particle size distributions and size-dependent particle composition. A closure assessment has been carried out that allowed for determination of the average hygroscopic growth factors (GF) at 85% relative humidity and the dimensionless hygroscopicity parameter ? for oxygenated organic aerosol (OA) and for supermicron particles, yielding ? = 0.1–0.15 and 0.9–1.0, respectively. The derived range of oxygenated OA ? values are in line with previous observations. The relatively large values for supermicron particles is consistent with substantial contributions of sea salt-containing particles in this size range. Analysis of time-dependent variations in the supermicron particle hygroscopicity suggest that atmospheric processing, specifically chloride displacement by nitrate and the accumulation of secondary organics on supermicron particles, can lead to substantial depression of the observed GF.

  18. Aerosol can waste disposal device

    DOE Patents [OSTI]

    O'Brien, Michael D. (Las Vegas, NV); Klapperick, Robert L. (Las Vegas, NV); Bell, Chris (Las Vegas, NV)

    1993-01-01

    Disclosed is a device for removing gases and liquid from containers. The ice punctures the bottom of a container for purposes of exhausting gases and liquid from the container without their escaping into the atmosphere. The device includes an inner cup or cylinder having a top portion with an open end for receiving a container and a bottom portion which may be fastened to a disposal or waste container in a substantially leak-proof manner. A piercing device is mounted in the lower portion of the inner cylinder for puncturing the can bottom placed in the inner cylinder. An outer cylinder having an open end and a closed end fits over the top portion of the inner cylinder in telescoping engagement. A force exerted on the closed end of the outer cylinder urges the bottom of a can in the inner cylinder into engagement with the piercing device in the bottom of the inner cylinder to form an opening in the can bottom, thereby permitting the contents of the can to enter the disposal container.

  19. Aerosol can waste disposal device

    DOE Patents [OSTI]

    O'Brien, M.D.; Klapperick, R.L.; Bell, C.

    1993-12-21

    Disclosed is a device for removing gases and liquid from containers. The device punctures the bottom of a container for purposes of exhausting gases and liquid from the container without their escaping into the atmosphere. The device includes an inner cup or cylinder having a top portion with an open end for receiving a container and a bottom portion which may be fastened to a disposal or waste container in a substantially leak-proof manner. A piercing device is mounted in the lower portion of the inner cylinder for puncturing the can bottom placed in the inner cylinder. An outer cylinder having an open end and a closed end fits over the top portion of the inner cylinder in telescoping engagement. A force exerted on the closed end of the outer cylinder urges the bottom of a can in the inner cylinder into engagement with the piercing device in the bottom of the inner cylinder to form an opening in the can bottom, thereby permitting the contents of the can to enter the disposal container. 7 figures.

  20. Spectrometer for Sky-Scanning Sun-Tracking Atmospheric Research (4STAR): Instrument Technology

    SciTech Connect (OSTI)

    Dunagan, Stephen; Johnson, Roy; Zavaleta, Jhony; Russell, P. B.; Schmid, Beat; Flynn, Connor J.; Redemann, Jens; Shinozuka, Yohei; Livingston, J.; Segal Rozenhaimer, Michal

    2013-08-06

    The Spectrometer for Sky-Scanning, Sun-Tracking Atmospheric Research (4STAR) combines airborne sun tracking and sky scanning with diffraction spectroscopy, to improve knowledge of atmospheric constituents and their links to air-pollution/climate. Direct beam hyper-spectral measurement of optical depth improves retrievals of gas constituents and determination of aerosol properties. Sky scanning enhances retrievals of aerosol type and size distribution. 4STAR measurements will tighten the closure between satellite and ground-based measurements. 4STAR incorporates a modular sun-tracking/ sky-scanning optical head with fiber optic signal transmission to rack mounted spectrometers, permitting miniaturization of the external optical head, and future detector evolution. Technical challenges include compact optical collector design, radiometric dynamic range and stability, and broad spectral coverage. Test results establishing the performance of the instrument against the full range of operational requirements are presented, along with calibration, engineering flight test, and scientific field campaign data and results.

  1. Strategy Implementation for the CTA Atmospheric Monitoring Program

    E-Print Network [OSTI]

    Doro, M; Reyes, R de los; Gaug, M; Maccarone, M C

    2015-01-01

    The Cherenkov Telescope Array (CTA) is the next generation facility of Imaging Atmospheric Cherenkov Telescopes. It will reach unprecedented sensitivity and energy resolution in very-high-energy gamma-ray astronomy. CTA will detect Cherenkov light emitted within an atmospheric shower of particles initiated by cosmic-gamma rays or cosmic rays entering the Earth's atmosphere. From the combination of images the Cherenkov light produces in the telescopes, one is able to infer the primary particle energy and direction. A correct energy estimation can be thus performed only if the local atmosphere is well characterized. The atmosphere not only affects the shower development itself, but also the Cherenkov photon transmission from the emission point in the particle shower, at about 10-20 km above the ground, to the detector. Cherenkov light on the ground is peaked in the UV-blue region, and therefore molecular and aerosol extinction phenomena are important. The goal of CTA is to control systematics in energy reconstr...

  2. Atmospheric sensing for the H.E.S.S. array

    SciTech Connect (OSTI)

    Aye, K.-M.; Brown, A.M.; Chadwick, P.M.; Hadjichristidis, C.; Latham, I.J.; Le Gallou, R.; McComb, T.J.L.; Nolan, S.J.; Noutsos, A.; Orford, K.J.; Osborne, J.L.; Rayner, S.M.

    2005-02-21

    Several atmospheric monitoring instruments have been installed at the H.E.S.S. gamma-ray observatory in Namibia. Firstly, Heitronics KT19 infrared radiometers, aligned paraxially with the H.E.S.S. telescopes, measure the infrared radiation of the water molecules. These allow us to detect clouds crossing the telescopes' field of view and to estimate the humidity present in the atmosphere. For a general estimate of the atmosphere's transmittance, i.e. the detection of any light-attenuating aerosols, a ceilometer, which is a LIDAR with built-in atmospheric data reduction code, is being used. It will be complemented soon by an instrument which will measure the transmissivity of the atmosphere at different wavelengths up to 500m above the ground. The overall status of the weather is monitored by a fully automated weatherstation. This paper describes the setup, the data analysis and how this will be used in order to improve the knowledge of the telescopes' effective collection area.

  3. Strategic Environmental Research and Development Program: Atmospheric Remote Sensing and Assessment Program -- Final Report. Part 1: The lower atmosphere

    SciTech Connect (OSTI)

    Tooman, T.P.

    1997-01-01

    This report documents work done between FY91 and FY95 for the lower atmospheric portion of the joint Department of Defense (DoD) and Department of Energy (DOE) Atmospheric Remote Sensing and Assessment Program (ARSAP) within the Strategic Environmental Research and Development Program (SERDP). The work focused on (1) developing new measurement capabilities and (2) measuring atmospheric heating in a well-defined layer and then relating it to cloud properties an water vapor content. Seven new instruments were develop3ed for use with Unmanned Aerospace Vehicles (UAVs) as the host platform for flux, radiance, cloud, and water vapor measurements. Four major field campaigns were undertaken to use these new as well as existing instruments to make critically needed atmospheric measurements. Scientific results include the profiling of clear sky fluxes from near surface to 14 km and the strong indication of cloudy atmosphere absorption of solar radiation considerably greater than predicted by extant models.

  4. Total aerosol effect: forcing or radiative flux perturbation?

    SciTech Connect (OSTI)

    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.

  5. Climate Engineering with Stratospheric Aerosols and Associated Engineering Parameters

    SciTech Connect (OSTI)

    Kravitz, Benjamin S.

    2013-02-12

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

  6. Rice straw burning in Southeast Asia as a source of CO and COS to the atmosphere

    SciTech Connect (OSTI)

    Nguyen, B.C.; Mihalopoulos, N.; Putaud, J.P. [Centre des Faibles Radioactivites, Gif-sur-Yvette (France)

    1994-08-20

    This paper discusses the results of aerosol monitoring field tests conducted in four locations in Viet Nam during 1992 and 1993. Atmospheric samples were collected during the dry and wet seasons during the time when rice straw burning was taking place in the agricultural rangelands. The samples were analyzed for carbon monoxide, carbon dioxide, and carbonyl sulfide. Experimental methods and implications of the analytical results are described. 21 refs., 2 figs., 3 tabs.

  7. Elisa Carboni1, Roy Grainger1, Gareth Thomas1, Andy Sayer1,2,

    E-Print Network [OSTI]

    sensitivity to the aerosol vertical distribution, surface temperature and atmospheric profile. and 0, extinction profile concentration) Sun-photometer: Plymouth, Chilbolton-Aeronet,Sun-photometer: Plymouth, Chilbolton-Aeronet, Cambridge-microtop. (AOD, size distribution) Radiosonde: particle profile ( ash

  8. Design of Aerosol Face Masks for Children Using Computerized 3D Face Analysis

    E-Print Network [OSTI]

    Kimmel, Ron

    seal to the child's face, and thus may minimize aerosol leakage and dead space. Key words: inhaled supplied with valved aerosol hold- ing chambers used for aerosol therapy. (Adapted with per- mission from

  9. Ensemble Atmospheric Dispersion Modeling

    SciTech Connect (OSTI)

    Addis, R.P.

    2002-06-24

    Prognostic atmospheric dispersion models are used to generate consequence assessments, which assist decision-makers in the event of a release from a nuclear facility. Differences in the forecast wind fields generated by various meteorological agencies, differences in the transport and diffusion models, as well as differences in the way these models treat the release source term, result in differences in the resulting plumes. Even dispersion models using the same wind fields may produce substantially different plumes. This talk will address how ensemble techniques may be used to enable atmospheric modelers to provide decision-makers with a more realistic understanding of how both the atmosphere and the models behave.

  10. The Statistical Evolution of Multiple Generations of Oxidation Products in the Photochemical Aging of Chemically Reduced Organic Aerosol

    SciTech Connect (OSTI)

    Wilson, Kevin R.; Smith, Jared D.; Kessler, Sean; Kroll, Jesse H.

    2011-10-03

    The heterogeneous reaction of hydroxyl radicals (OH) with squalane and bis(2-ethylhexyl) sebacate (BES) particles are used as model systems to examine how distributions of reactionproducts evolve during the oxidation of chemically reduced organic aerosol. A kinetic model of multigenerational chemistry, which is compared to previously measured (squalane) and new(BES) experimental data, reveals that it is the statistical mixtures of different generations of oxidation products that control the average particle mass and elemental composition during thereaction. The model suggests that more highly oxidized reaction products, although initially formed with low probability, play a large role in the production of gas phase reaction products.In general, these results highlight the importance of considering atmospheric oxidation as a statistical process, further suggesting that the underlying distribution of molecules could playimportant roles in aerosol formation as well as in the evolution of key physicochemical properties such as volatility and hygroscopicity.

  11. Atmospheric Properties from the 2006 Niamey Deployment and Climate Simulation with a Geodesic Grid Coupled Climate Model Third Quarter 2008

    SciTech Connect (OSTI)

    JH Mather; DA Randall; CJ Flynn

    2008-06-30

    In 2008, the Atmospheric Radiation Measurement (ARM) Program and the Climate Change Prediction Program (CCPP) have been asked to produce joint science metrics. For CCPP, the metrics will deal with a decade-long control simulation using geodesic grid-coupled climate model. For ARM, the metrics will deal with observations associated with the 2006 deployment of the ARM Mobile Facility (AMF) to Niamey, Niger. Specifically, ARM has been asked to deliver data products for Niamey that describe cloud, aerosol, and dust properties. This report describes the aerosol optical depth (AOD) product.

  12. The oceanic cycle and global atmospheric budget of carbonyl sulfide

    SciTech Connect (OSTI)

    Weiss, P.S.

    1994-12-31

    A significant portion of stratospheric air chemistry is influenced by the existence of carbonyl sulfide (COS). This ubiquitous sulfur gas represents a major source of sulfur to the stratosphere where it is converted to sulfuric acid aerosol particles. Stratospheric aerosols are climatically important because they scatter incoming solar radiation back to space and are able to increase the catalytic destruction of ozone through gas phase reactions on particle surfaces. COS is primarily formed at the surface of the earth, in both marine and terrestrial environments, and is strongly linked to natural biological processes. However, many gaps in the understanding of the global COS cycle still exist, which has led to a global atmospheric budget that is out of balance by a factor of two or more, and a lack of understanding of how human activity has affected the cycling of this gas. The goal of this study was to focus on COS in the marine environment by investigating production/destruction mechanisms and recalculating the ocean-atmosphere flux.

  13. Challenge the future 1 Observations of aerosol-cloud-radiation

    E-Print Network [OSTI]

    Graaf, Martin de

    -road Industrial coal Residential solid fuel Biofuel cooking Biofuel heating Coal Open Burning Agricultural fields causes Differences in: · cloud properties · cloud fraction and location · aerosol properties · smoke

  14. Extending the physicochemical characterization of aerosol particles in California

    E-Print Network [OSTI]

    Zauscher, Melanie Dorothy

    2012-01-01

    W. T. (1997).Emissions from Smoldering Combustion of BiomassCombustion generated aerosols, including emissions from diesel and gasoline engines, biomass and

  15. Relating Secondary Organic Aerosol Characteristics with Cloud Condensation Nuclei Activity

    E-Print Network [OSTI]

    Tang, Xiaochen

    2013-01-01

    by V and Ni from heavy oil combustion: Anthropogenic sourcesgeneration from heavy fuel oil (HFO) as an alternative toengines operating with heavy fuel oils. Journal of Aerosol

  16. The Radiative Role of Free Tropospheric Aerosols and Marine Clouds...

    Office of Scientific and Technical Information (OSTI)

    Technical Report: The Radiative Role of Free Tropospheric Aerosols and Marine Clouds over the Central North Atlantic Citation Details In-Document Search Title: The Radiative Role...

  17. Clear sky atmosphere at cm-wavelengths from climatology data

    E-Print Network [OSTI]

    Lew, Bartosz

    2015-01-01

    We utilise ground-based, balloon-born and satellite climatology data to reconstruct site and season-dependent vertical profiles of precipitable water vapour (PWV). We use these profiles to numerically solve radiative transfer through the atmosphere, and derive atmospheric brightness temperature ($T_{\\rm atm}$) and optical depth ($\\tau$) at the centimetre wavelengths. We validate the reconstruction by comparing the model column PWV, with photometric measurements of PWV, performed in the clear sky conditions towards the Sun. Based on the measurements, we devise a selection criteria to filter the climatology data to match the PWV levels to the expectations of the clear sky conditions. We apply the reconstruction to the location of the Polish 32-metre radio telescope, and characterise $T_{\\rm atm}$ and $\\tau$ year-round, at selected frequencies. We also derive the zenith distance dependence for these parameters, and discuss shortcomings of using planar, single-layer, and optically thin atmospheric model approxima...

  18. Autumn 2014 Atmospheric Circulation

    E-Print Network [OSTI]

    Doty, Sharon Lafferty

    to perform atmospheric chemistry measurements in this remote region of ubiquitous oil and gas drilling 30 days they raised $12,000, enough to support Maria's travel to Utah and to cover the costs

  19. Abel transform inversion of radio occultation measurements made with a receiver inside the Earth's atmosphere.

    E-Print Network [OSTI]

    Haase, Jennifer

    with an Abel transform to give a vertical profile of refractive index and subsequently temperature an estimate of the atmospheric refractive index profile. The measurement geometry is closely related to problems encountered when inverting seismic time­travel data and solar occultation measurements, where

  20. Instant Profiling: Instrumentation Sampling for Profiling Datacenter Applications

    E-Print Network [OSTI]

    Cortes, Corinna

    Instant Profiling: Instrumentation Sampling for Profiling Datacenter Applications Hyoun Kyu Cho Profile-guided optimization possesses huge potential to save costs for datacenters. Hardware performance programmers find code regions to optimize by monitoring datacenter applications continuously on live traffic

  1. OH-initiated heterogeneous aging of highly oxidized organic aerosol

    E-Print Network [OSTI]

    Kessler, Sean H.

    2013-01-01

    Abbatt, J. P. D. Atmospheric Chemistry and Physics 2007, 7,Wilson, K. R. Atmospheric Chemistry and Physics DiscussionsKanakidou, M. et al. Atmospheric Chemistry and Physics 2005,

  2. Chemical and Physical Investigation of Secondary Organic Aerosol Formation

    E-Print Network [OSTI]

    Nakao, Shunsuke

    2012-01-01

    Saunders, R. W. : Atmospheric Chemistry of Iodine, Chemicalmodelling: a review, Atmospheric Chemistry and Physics, 5,emerging issues, Atmospheric Chemistry and Physics, 9, 5155-

  3. JP2.3 CLOUD RADIATIVE HEATING RATE FORCING FROM PROFILES OF RETRIEVED ARCTIC CLOUD MICROPHYSICS

    E-Print Network [OSTI]

    Shupe, Matthew

    JP2.3 CLOUD RADIATIVE HEATING RATE FORCING FROM PROFILES OF RETRIEVED ARCTIC CLOUD MICROPHYSICS). This data allows for observationally-based calculations ofradiative heating rate profiles within the Arctic atmosphere. In this paper we define cloud radiative heating rate forcing (CRHF) as the difference between

  4. Transport and mixing patterns over Central California during the carbonaceous aerosol and radiative effects study (CARES)

    SciTech Connect (OSTI)

    Fast J. D.; Springston S.; Gustafson Jr., W. I.; Berg, L. K.; Shaw, W. J.; Pekour, M.; Shrivastava, M.; Barnard, J. C.; Ferrare, R. A.; Hostetler, C. A.; Hair, J. A.; Erickson, M.; Jobson, B. T.; Flowers, B.; Dubey, M. K.; Pierce, R. B.; Dolislager, L.; Pederson, J.; Zaveri, R. A.

    2012-02-17

    We describe the synoptic and regional-scale meteorological conditions that affected the transport and mixing of trace gases and aerosols in the vicinity of Sacramento, California during June 2010 when the Carbonaceous Aerosol and Radiative Effects Study (CARES) was conducted. The meteorological measurements collected by various instruments deployed during the campaign and the performance of the chemistry version of the Weather Research and Forecasting model (WRF-Chem) are both discussed. WRF-Chem was run daily during the campaign to forecast the spatial and temporal variation of carbon monoxide emitted from 20 anthropogenic source regions in California to guide aircraft sampling. The model is shown to reproduce the overall circulations and boundary-layer characteristics in the region, although errors in the upslope wind speed and boundary-layer depth contribute to differences in the observed and simulated carbon monoxide. Thermally-driven upslope flows that transported pollutants from Sacramento over the foothills of the Sierra Nevada occurred every afternoon, except during three periods when the passage of mid-tropospheric troughs disrupted the regional-scale flow patterns. The meteorological conditions after the passage of the third trough were the most favorable for photochemistry and likely formation of secondary organic aerosols. Meteorological measurements and model forecasts indicate that the Sacramento pollutant plume was likely transported over a downwind site that collected trace gas and aerosol measurements during 23 time periods; however, direct transport occurred during only eight of these periods. The model also showed that emissions from the San Francisco Bay area transported by intrusions of marine air contributed a large fraction of the carbon monoxide in the vicinity of Sacramento, suggesting that this source likely affects local chemistry. Contributions from other sources of pollutants, such as those in the Sacramento Valley and San Joaquin Valley, were relatively low. Aerosol layering in the free troposphere was observed during the morning by an airborne Lidar. WRF-Chem forecasts showed that mountain venting processes contributed to aged pollutants aloft in the valley atmosphere that are then entrained into the growing boundary layer the subsequent day.

  5. Transport and Mixing Patterns over Central California during the Carbonaceous Aerosol and Radiative Effects Study (CARES)

    SciTech Connect (OSTI)

    Fast, Jerome D.; Gustafson, William I.; Berg, Larry K.; Shaw, William J.; Pekour, Mikhail S.; Shrivastava, ManishKumar B.; Barnard, James C.; Ferrare, R.; Hostetler, Chris A.; Hair, John; Erickson, Matthew H.; Jobson, Tom; Flowers, Bradley; Dubey, Manvendra K.; Springston, Stephen R.; Pirce, Bradley R.; Dolislager, Leon; Pederson, J. R.; Zaveri, Rahul A.

    2012-02-17

    We describe the synoptic and regional-scale meteorological conditions that affected the transport and mixing of trace gases and aerosols in the vicinity of Sacramento, California during June 2010 when the Carbonaceous Aerosol and Radiative Effects Study (CARES) was conducted. The meteorological measurements collected by various instruments deployed during the campaign and the performance of the chemistry version of the Weather Research and Forecasting model (WRF-Chem) are both discussed. WRF-Chem was run daily during the campaign to forecast the spatial and temporal variation of carbon monoxide emitted from 20 anthropogenic source regions in California to guide aircraft sampling. The model is shown to reproduce the overall circulations and boundary-layer characteristics in the region, although errors in the upslope wind speed and boundary-layer depth contribute to differences in the observed and simulated carbon monoxide. Thermally-driven upslope flows that transported pollutants from Sacramento over the foothills of the Sierra Nevada occurred every afternoon, except during three periods when the passage of mid-tropospheric troughs disrupted the regional-scales flow patterns. The meteorological conditions after the passage of the third trough were the most favorable for photochemistry and likely formation of secondary organic aerosols. Meteorological measurements and model forecasts indicate that the Sacramento pollutant plume was likely transported over a downwind site that collected trace gas and aerosol measurements during 23 periods; however, direct transport occurred during only eight of these periods. The model also showed that emissions from the San Francisco Bay area transported by intrusions of marine air contributed a large fraction of the carbon monoxide in the vicinity of Sacramento, suggesting that this source likely affects local chemistry. Contributions from other sources of pollutants, such as those in the Sacramento Valley and San Joaquin Valley, were relatively low. Aerosol layering in the free troposphere was observed during the morning by an airborne Lidar; WRF-Chem forecasts showed that mountain venting processes contributed to aged pollutants aloft in the valley atmosphere which then can be entrained into the growing boundary layer the subsequent day.

  6. Transport of anthropogenic and biomass burning aerosols from Europe to the Arctic during spring 2008

    SciTech Connect (OSTI)

    Marelle, L.; Raut, Jean-Christophe; Thomas, J. L.; Law, K. S.; Quennehen, Boris; Ancellet, G.; Pelon, J.; Schwarzenboeck, A.; Fast, Jerome D.

    2015-04-10

    During the POLARCAT-France airborne campaign in April 2008, pollution originating from anthropogenic and biomass burning emissions was measured in the European Arctic. We compare these aircraft measurements with simulations using the WRF-Chem model to investigate model representation of aerosols transported from Europe to the Arctic. Modeled PM2.5 is evaluated using European Monitoring and Evaluation Programme (EMEP) measurements in source regions and POLARCAT aircraft measurements in the Scandinavian Arctic. Total PM2.5 agrees well with the measurements, although the model overestimates nitrate and underestimates organic carbon in source regions. Using WRF-Chem in combination with the Lagrangian model FLEXPART-WRF, we find that during the campaign the research aircraft sampled two different types of European plumes: mixed anthropogenic and fire plumes from eastern Europe and Russia transported below 2 km, and anthropogenic plumes from central Europe uplifted by warm conveyor belt circulations to 5–6 km. Both modeled plume types had undergone significant wet scavenging (> 50% PM10) during transport. Modeled aerosol vertical distributions and optical properties below the aircraft are evaluated in the Arctic using airborne lidar measurements. Model results show that the pollution event transported aerosols into the Arctic (> 66.6° N) for a 4-day period. During this 4-day period, biomass burning emissions have the strongest influence on concentrations between 2.5 and 3 km altitudes, while European anthropogenic emissions influence aerosols at both lower (~ 1.5 km) and higher altitudes (~ 4.5 km). As a proportion of PM2.5, modeled black carbon and SO4= concentrations are more enhanced near the surface in anthropogenic plumes. The European plumes sampled during the POLARCAT-France campaign were transported over the region of springtime snow cover in northern Scandinavia, where they had a significant local atmospheric warming effect. We find that, during this transport event, the average modeled top-of-atmosphere (TOA) shortwave direct and semi-direct radiative effect (DSRE) north of 60° N over snow and ice-covered surfaces reaches +0.58 W m?2, peaking at +3.3 W m?2 at noon over Scandinavia and Finland.

  7. Transport of anthropogenic and biomass burning aerosols from Europe to the Arctic during spring 2008

    SciTech Connect (OSTI)

    Marelle, L.; Raut, Jean-Christophe; Thomas, J. L.; Law, K. S.; Quennehen, Boris; Ancellet, G.; Pelon, J.; Schwarzenboeck, A.; Fast, Jerome D.

    2015-01-01

    During the POLARCAT-France airborne campaign in April 2008, pollution originating from anthropogenic and biomass burning emissions was measured in the European Arctic. We compare these aircraft measurements with simulations using the WRF-Chem model to investigate model representation of aerosols transported from Europe to the Arctic. Modeled PM2.5 is evaluated using European Monitoring and Evaluation Programme (EMEP) measurements in source regions and POLARCAT aircraft measurements in the Scandinavian Arctic. Total PM2.5 agrees well with the measurements, although the model overestimates nitrate and underestimates organic carbon in source regions. Using WRF-Chem in combination with the Lagrangian model FLEXPART-WRF, we find that during the campaign the research aircraft sampled two different types of European plumes: mixed anthropogenic and fire plumes from eastern Europe and Russia transported below 2 km, and anthropogenic plumes from central Europe uplifted by warm conveyor belt circulations to 5–6 km. Both modeled plume types had undergone significant wet scavenging (> 50% PM10) during transport. Modeled aerosol vertical distributions and optical properties below the aircraft are evaluated in the Arctic using airborne lidar measurements. Model results show that the pollution event transported aerosols into the Arctic (> 66.6° N) for a 4-day period. During this 4-day period, biomass burning emissions have the strongest influence on concentrations between 2.5 and 3 km altitudes, while European anthropogenic emissions influence aerosols at both lower (~ 1.5 km) and higher altitudes (~ 4.5 km). As a proportion of PM2.5, modeled black carbon and SO4= concentrations are more enhanced near the surface in anthropogenic plumes. The European plumes sampled during the POLARCAT-France campaign were transported over the region of springtime snow cover in northern Scandinavia, where they had a significant local atmospheric warming effect. We find that, during this transport event, the average modeled top-of-atmosphere (TOA) shortwave direct and semi-direct radiative effect (DSRE) north of 60° N over snow and ice-covered surfaces reaches +0.58 W m?2, peaking at +3.3 W m?2 at noon over Scandinavia and Finland.

  8. Transport of anthropogenic and biomass burning aerosols from Europe to the Arctic during spring 2008

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Marelle, L.; Raut, Jean-Christophe; Thomas, J. L.; Law, K. S.; Quennehen, Boris; Ancellet, G.; Pelon, J.; Schwarzenboeck, A.; Fast, Jerome D.

    2015-04-10

    During the POLARCAT-France airborne campaign in April 2008, pollution originating from anthropogenic and biomass burning emissions was measured in the European Arctic. We compare these aircraft measurements with simulations using the WRF-Chem model to investigate model representation of aerosols transported from Europe to the Arctic. Modeled PM2.5 is evaluated using European Monitoring and Evaluation Programme (EMEP) measurements in source regions and POLARCAT aircraft measurements in the Scandinavian Arctic. Total PM2.5 agrees well with the measurements, although the model overestimates nitrate and underestimates organic carbon in source regions. Using WRF-Chem in combination with the Lagrangian model FLEXPART-WRF, we find that duringmore »the campaign the research aircraft sampled two different types of European plumes: mixed anthropogenic and fire plumes from eastern Europe and Russia transported below 2 km, and anthropogenic plumes from central Europe uplifted by warm conveyor belt circulations to 5–6 km. Both modeled plume types had undergone significant wet scavenging (> 50% PM10) during transport. Modeled aerosol vertical distributions and optical properties below the aircraft are evaluated in the Arctic using airborne lidar measurements. Model results show that the pollution event transported aerosols into the Arctic (> 66.6° N) for a 4-day period. During this 4-day period, biomass burning emissions have the strongest influence on concentrations between 2.5 and 3 km altitudes, while European anthropogenic emissions influence aerosols at both lower (~ 1.5 km) and higher altitudes (~ 4.5 km). As a proportion of PM2.5, modeled black carbon and SO4= concentrations are more enhanced near the surface in anthropogenic plumes. The European plumes sampled during the POLARCAT-France campaign were transported over the region of springtime snow cover in northern Scandinavia, where they had a significant local atmospheric warming effect. We find that, during this transport event, the average modeled top-of-atmosphere (TOA) shortwave direct and semi-direct radiative effect (DSRE) north of 60° N over snow and ice-covered surfaces reaches +0.58 W m?2, peaking at +3.3 W m?2 at noon over Scandinavia and Finland.« less

  9. Technical Note: On the use of nudging for aerosol–climate model intercomparison studies

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

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

    2014-08-26

    Nudging as an assimilation technique has seen increased use in recent years in the development and evaluation of climate models. Constraining the simulated wind and temperature fields using global weather reanalysis facilitates more straightforward comparison between simulation and observation, and reduces uncertainties associated with natural variabilities of the large-scale circulation. On the other hand, the forcing introduced by nudging can be strong enough to change the basic characteristics of the model climate. In the paper we show that for the Community Atmosphere Model version 5 (CAM5), due to the systematic temperature bias in the standard model and the sensitivity ofmore »simulated ice formation to anthropogenic aerosol concentration, nudging towards reanalysis results in substantial reductions in the ice cloud amount and the impact of anthropogenic aerosols on long-wave cloud forcing. In order to reduce discrepancies between the nudged and unconstrained simulations, and meanwhile take the advantages of nudging, two alternative experimentation methods are evaluated. The first one constrains only the horizontal winds. The second method nudges both winds and temperature, but replaces the long-term climatology of the reanalysis by that of the model. Results show that both methods lead to substantially improved agreement with the free-running model in terms of the top-of-atmosphere radiation budget and cloud ice amount. The wind-only nudging is more convenient to apply, and provides higher correlations of the wind fields, geopotential height and specific humidity between simulation and reanalysis. Results from both CAM5 and a second aerosol–climate model ECHAM6-HAM2 also indicate that compared to the wind-and-temperature nudging, constraining only winds leads to better agreement with the free-running model in terms of the estimated shortwave cloud forcing and the simulated convective activities. This suggests nudging the horizontal winds but not temperature is a good strategy for the investigation of aerosol indirect effects since it provides well-constrained meteorology without strongly perturbing the model's mean climate.« less

  10. EIA - State Nuclear Profiles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration would like submitKansas Nuclear Profile 2010 Kansas profile KansasHampshire Nuclear Profile 2010

  11. EIA - State Nuclear Profiles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration would like submitKansas Nuclear Profile 2010 Kansas profile KansasHampshire Nuclear Profile

  12. EIA - State Nuclear Profiles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration would like submitKansas Nuclear Profile 2010 Kansas profile KansasHampshire Nuclear ProfileYork

  13. EIA - State Nuclear Profiles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration would like submitKansas Nuclear Profile 2010 Kansas profile KansasHampshireTexas profile Texas

  14. EIA - State Nuclear Profiles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration would like submitKansas Nuclear Profile 2010 Kansas profile KansasHampshireTexas profile

  15. EIA - State Nuclear Profiles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration would like submitKansas Nuclear Profile 2010 Kansas profile KansasHampshireTexas profileVirginia

  16. Simulation and Theory of Ions at Atmospherically Relevant Aqueous Liquid-Air Interfaces

    E-Print Network [OSTI]

    Douglas J. Tobias; Abraham C. Stern; Marcel D. Baer; Yan Levin; Christopher J. Mundy

    2013-06-28

    Chemistry occurring at or near the surfaces of aqueous droplets and thin films in the atmosphere influences air quality and climate. Molecular dynamics simulations are becoming increasingly useful for gaining atomic-scale insight into the structure and reactivity of aqueous interfaces in the atmosphere. Here we review simulation studies of atmospherically relevant aqueous liquid-air interfaces, with an emphasis on ions that play important roles in the chemistry of atmospheric aerosols. In addition to surveying results from simulation studies, we discuss challenges to the refinement and experimental validation of the methodology for simulating ion adsorption to the air-water interface, and recent advances in elucidating the driving forces for adsorption. We also review the recent development of a dielectric continuum theory that is capable of reproducing simulation and experimental data on ion behavior at aqueous interfaces.

  17. Chemical aging of single and multicomponent biomass burning aerosol surrogate-particles by OH: Implications for cloud condensation nucleus activity

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Thalman, R.; Thalman, R.; Wang, J.; Knopf, D. A.

    2015-01-01

    Multiphase OH and O? oxidation reactions with atmospheric organic aerosol (OA) can influence particle physicochemical properties including composition, morphology, and lifetime. Chemical aging of initially insoluble or low soluble single-component OA by OH and O? can increase their water-solubility and hygroscopicity, making them more active as cloud condensation nuclei (CCN) and susceptible to wet deposition. However, an outstanding problem is whether the effects of chemical aging on their CCN activity are preserved when mixed with other organic or inorganic compounds exhibiting greater water-solubility. In this work, the CCN activity of laboratory-generated biomass burning aerosol (BBA) surrogate-particles exposed to OH andmore »O? is evaluated by determining the hygroscopicity parameter, ?, as a function of particle type, mixing state, and OH/O? exposure applying a CCN counter (CCNc) coupled to an aerosol flow reactor (AFR). Levoglucosan (LEV), 4-methyl-5-nitrocatechol (MNC), and potassium sulfate (KS) serve as representative BBA compounds that exhibit different hygroscopicity, water solubility, chemical functionalities, and reactivity with OH radicals, and thus exemplify the complexity of mixed inorganic/organic aerosol in the atmosphere. The CCN activities of all of the particles were unaffected by O? exposure. Following exposure to OH, ? of MNC was enhanced by an order of magnitude, from 0.009 to ~0.1, indicating that chemically-aged MNC particles are better CCN and more prone to wet deposition than pure MNC particles. No significant enhancement in ? was observed for pure LEV particles following OH exposure. ? of the internally-mixed particles was not affected by OH oxidation. Furthermore, the CCN activity of OH exposed MNC-coated KS particles is similar to the OH unexposed atomized 1:1 by mass MNC: KS binary-component particles. Our results strongly suggest that when OA is dominated by water-soluble organic carbon (WSOC) or inorganic ions, chemical aging has no significant impact on OA hygroscopicity. The organic compounds exhibiting low solubility behave as if they are infinitely soluble when mixed with a sufficient amount of water-soluble compounds. At and beyond this point, the particles' CCN activity is governed entirely by the water-soluble fraction and not influenced by the oxidized organic fraction. Our results have important implications for heterogeneous oxidation and its impact on cloud formation given that atmospheric aerosol is a complex mixture of organic and inorganic compounds exhibiting a wide-range of solubilities.« less

  18. Chemical aging of single and multicomponent biomass burning aerosol surrogate particles by OH: implications for cloud condensation nucleus activity

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Slade, J. H.; Thalman, R.; Wang, J.; Knopf, D. A.

    2015-09-14

    Multiphase OH and O3 oxidation reactions with atmospheric organic aerosol (OA) can influence particle physicochemical properties including composition, morphology, and lifetime. Chemical aging of initially insoluble or low-soluble single-component OA by OH and O3 can increase their water solubility and hygroscopicity, making them more active as cloud condensation nuclei (CCN) and susceptible to wet deposition. However, an outstanding problem is whether the effects of chemical aging on their CCN activity are preserved when mixed with other organic or inorganic compounds exhibiting greater water solubility. In this work, the CCN activity of laboratory-generated biomass burning aerosol (BBA) surrogate particles exposed tomore »OH and O3 is evaluated by determining the hygroscopicity parameter, ?, as a function of particle type, mixing state, and OH and O3 exposure applying a CCN counter (CCNc) coupled to an aerosol flow reactor (AFR). Levoglucosan (LEV), 4-methyl-5-nitrocatechol (MNC), and potassium sulfate (KS) serve as representative BBA compounds that exhibit different hygroscopicity, water solubility, chemical functionalities, and reactivity with OH radicals, and thus exemplify the complexity of mixed inorganic/organic aerosol in the atmosphere. The CCN activities of all of the particles were unaffected by O3 exposure. Following exposure to OH, ? of MNC was enhanced by an order of magnitude, from 0.009 to ~ 0.1, indicating that chemically aged MNC particles are better CCN and more prone to wet deposition than pure MNC particles. No significant enhancement in ? was observed for pure LEV particles following OH exposure. ? of the internally mixed particles was not affected by OH oxidation. Furthermore, the CCN activity of OH-exposed MNC-coated KS particles is similar to the OH unexposed atomized 1 : 1 by mass MNC : KS binary-component particles. Our results strongly suggest that when OA is dominated by water-soluble organic carbon (WSOC) or inorganic ions, chemical aging has no significant impact on OA hygroscopicity. The organic compounds exhibiting low solubility behave as if they are infinitely soluble when mixed with a sufficient number of water-soluble compounds. At and beyond this point, the particles' CCN activity is governed entirely by the water-soluble fraction and is not influenced by the oxidized organic fraction. Our results have important implications for heterogeneous oxidation and its impact on cloud formation given that atmospheric aerosol is a complex mixture of organic and inorganic compounds exhibiting a wide range of solubilities.« less

  19. Chemical aging of single and multicomponent biomass burning aerosol surrogate-particles by OH: implications for cloud condensation nucleus activity

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Slade, J. H.; Thalman, R.; Wang, J.; Knopf, D. A.

    2015-03-06

    Multiphase OH and O3 oxidation reactions with atmospheric organic aerosol (OA) can influence particle physicochemical properties including composition, morphology, and lifetime. Chemical aging of initially insoluble or low soluble single-component OA by OH and O3 can increase their water-solubility and hygroscopicity, making them more active as cloud condensation nuclei (CCN) and susceptible to wet deposition. However, an outstanding problem is whether the effects of chemical aging on their CCN activity are preserved when mixed with other organic or inorganic compounds exhibiting greater water-solubility. In this work, the CCN activity of laboratory-generated biomass burning aerosol (BBA) surrogate-particles exposed to OH andmore »O3 is evaluated by determining the hygroscopicity parameter, ?, as a function of particle type, mixing state, and OH/O3 exposure applying a CCN counter (CCNc) coupled to an aerosol flow reactor (AFR). Levoglucosan (LEV), 4-methyl-5-nitrocatechol (MNC), and potassium sulfate (KS) serve as representative BBA compounds that exhibit different hygroscopicity, water solubility, chemical functionalities, and reactivity with OH radicals, and thus exemplify the complexity of mixed inorganic/organic aerosol in the atmosphere. The CCN activities of all of the particles were unaffected by O3 exposure. Following exposure to OH, ? of MNC was enhanced by an order of magnitude, from 0.009 to ~0.1, indicating that chemically-aged MNC particles are better CCN and more prone to wet deposition than pure MNC particles. No significant enhancement in ? was observed for pure LEV particles following OH exposure. ? of the internally-mixed particles was not affected by OH oxidation. Furthermore, the CCN activity of OH exposed MNC-coated KS particles is similar to the OH unexposed atomized 1 : 1 by mass MNC : KS binary-component particles. Our results strongly suggest that when OA is dominated by water-soluble organic carbon (WSOC) or inorganic ions, chemical aging has no significant impact on OA hygroscopicity. The organic compounds exhibiting low solubility behave as if they are infinitely soluble when mixed with a sufficient amount of water-soluble compounds. At and beyond this point, the particles' CCN activity is governed entirely by the water-soluble fraction and not influenced by the oxidized organic fraction. Our results have important implications for heterogeneous oxidation and its impact on cloud formation given that atmospheric aerosol is a complex mixture of organic and inorganic compounds exhibiting a wide-range of solubilities.« less

  20. Observed high-altitude warming and snow cover retreat over Tibet and the Himalayas enhanced by black carbon aerosols

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Xu, Y.; Ramanathan, V.; Washington, W. M.

    2015-07-10

    Himalayan mountain glaciers and the snowpack over the Tibetan Plateau provide the headwater of several major rivers in Asia. In-situ observations of snow cover fraction since the 1960s suggest that the snow pack in the region have retreated significantly, accompanied by a surface warming of 2–2.5 °C observed over the peak altitudes (5000 m). Using a high-resolution ocean–atmosphere global climate model and an observationally constrained black carbon (BC) aerosol forcing, we attribute the observed altitude dependence of the warming trends as well as the spatial pattern of reductions in snow depths and snow cover fraction to various anthropogenic factors. Atmore »the Tibetan Plateau altitudes, the increase of atmospheric CO2 concentration exerted a warming of 1.7 °C, BC 1.3 °C where as cooling aerosols cause about 0.7 °C cooling, bringing the net simulated warming consistent with the anomalously large observed warming. We therefore conclude that BC together with CO2 has contributed to the snow retreat trends. Especially, BC increase is the major factor in the strong elevation dependence of the observed surface warming. The atmospheric warming by BC as well as its surface darkening of snow are coupled with the positive snow albedo feedbacks to account for the disproportionately large role of BC in high-elevation regions. These findings reveal that BC impact needs to be properly accounted for in future regional climate projections, in particular on high-altitude cryosphere.« less

  1. Polymer Physics Research Profile

    E-Print Network [OSTI]

    Giger, Christine

    Polymer Physics Research Profile Our main interests are the theory of simplification and some behavior on different autonomous levels of description. Our favorite applications range from polymer + Nonequilibrium Thermodynamics + Coarse Graining + Soft Matter + Polymer Physics + Rheology + Competences

  2. EIA - State Nuclear Profiles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration would like submitKansas Nuclear Profile 2010 Kansas profile Kansas total

  3. EIA - State Nuclear Profiles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration would like submitKansas Nuclear Profile 2010 Kansas profile Kansas

  4. Aerosol Science and Technology, 39:6883, 2005 Copyright c American Association for Aerosol Research

    E-Print Network [OSTI]

    . Coffman5 1 Finnish Meteorological Institute, Air Quality Research, Sahaajankatu, Helsinki, Finland 2¨ais¨al¨a Foundation (Finland), and the 100th Anniversary Foundation of Helsingin Sanomat (Finland). Address, 00880 Helsinki, Finland. E-mail: aki.virkkula@fmi.fi properties of aerosols depend on the wavelength

  5. Aerosol Science and Technology, 38:555573, 2004 Copyright c American Association for Aerosol Research

    E-Print Network [OSTI]

    Jimenez, Jose-Luis

    from motor vehicles are a significant source of fine particulate matter (PM) and gaseous pollutants of their emission. This work uses an Aero- dyne aerosol mass spectrometer (AMS) to provide size instrumentation, was deployed on the Aero- dyne Research Inc. (ARI) mobile laboratory, which was used to "chase

  6. Techniques for Minimizing Aerosols (aerosols are a common source of laboratoryacquired infections)

    E-Print Network [OSTI]

    Chan, Hue Sun

    " pipettes to avoid blowing out the last drop Drain pipettes gently with the tip against the inner wall glass rod to crack the glass, allow time for air to seep into the ampoule and gently remove the top than glass (less likely to break which generates aerosols) Source: Adapted from

  7. Role of ammonia chemistry and coarse mode aerosols in global climatological inorganic aerosol distributions

    E-Print Network [OSTI]

    Moore, Keith

    , the aerosolassociated water depends on the composition of the #12;3 particles, which is determined by gas in a three dimensional chemical transport model to understand the roles of ammonia chemistry and natural precursors among modeled aerosol species selfconsistently with ambient relative humidity and natural

  8. 13, 1479714822, 2013 Atmospheric waves

    E-Print Network [OSTI]

    Lovejoy, Shaun

    .5194/acpd-13-14797-2013 © Author(s) 2013. CC Attribution 3.0 License. Sciences ss Atmospheric Chemistry and Physics OpenAccess Atmospheric Chemistry and Physics OpenAccess Discussions Atmospheric Measurement s Discussions This discussion paper is/has been under review for the journal Atmospheric Chemistry and Physics

  9. SCIAMACHY'S ABSORBING AEROSOL INDEX AND THE CONSEQUENCES OF INSTRUMENT DEGRADATION

    E-Print Network [OSTI]

    Graaf, Martin de

    SCIAMACHY'S ABSORBING AEROSOL INDEX AND THE CONSEQUENCES OF INSTRUMENT DEGRADATION L. G. Tilstra1- itoring the Absorbing Aerosol Index (AAI) [1] measured by the satellite instrument SCIAMACHY [2]. We find. This we conclude from straightforward calculation of the effect of instrument degradation based

  10. Global observations of desert dust and biomass burning aerosols

    E-Print Network [OSTI]

    Graaf, Martin de

    and desert dust observations from GOME and SCIAMACHY · Conclusions and Outlook #12; · Absorbing Aerosol Transfer Model Solar zenith angle = 30° Viewing zenith angle = 0° Surface albedo = 5% #12;Reflectance at TOA with absorbing aerosols Doubling-Adding KNMI Radiative Transfer Model Solar zenith angle = 30

  11. GLOBAL AEROSOL EFFECT RETRIEVAL FROM PASSIVE HYPERSPECTRAL MEASUREMENTS

    E-Print Network [OSTI]

    Graaf, Martin de

    that can be detected using UV reflectance measurements. Since the aerosol extinction optical thickness any instrument, or a combination of instruments, that measures UV, visible and SWIR reflectancesGLOBAL AEROSOL EFFECT RETRIEVAL FROM PASSIVE HYPERSPECTRAL MEASUREMENTS M. de Graaf1,2 , L. G

  12. Organic Aerosol Formation Downwind from the Deepwater Horizon Oil Spill

    E-Print Network [OSTI]

    Toohey, Darin W.

    Organic Aerosol Formation Downwind from the Deepwater Horizon Oil Spill Nicole ONeill - ATOC 3500 and aerosol composition of air over the Deepwater Horizon oil spill in the Gulf of Mexico. · The lightest chemicals in the oil evaporated within hours, as scientists expected them to do. What they didn't expect

  13. Supplementary Material1 Characterization of Organic Aerosol Produced during2

    E-Print Network [OSTI]

    Meskhidze, Nicholas

    mass spectra of a dominant type (coal) of ambient aerosol in Shanghai using2 ATOFMS (m/z from 1501 Supplementary Material1 Characterization of Organic Aerosol Produced during2 Pulverized Coal diagram of combustion process of a single coal particle5 6 #12;3 10 100 10 3 10 4 10 5 Oxygen/coal ratio

  14. Effects of operating conditions on a heat transfer fluid aerosol 

    E-Print Network [OSTI]

    Sukmarg, Passaporn

    2000-01-01

    fluids are used as hot liquids at elevated pressures. If loss of containment does occur, the liquid will leak under pressure and may disperse as a fine aerosol mist. Though it has been recognized that aerosol mists can explode, very little is known about...

  15. Effects of aerosols on deep convective cumulus clouds 

    E-Print Network [OSTI]

    Fan, Jiwen

    2009-05-15

    in the droplet size. Ice processes are more sensitive to the changes of aerosol chemical properties than the warm rain processes. The most noticeable effect of increasing aerosol number concentrations is an increase of CDNC and cloud water content but a decrease...

  16. Flood or Drought: How Do Aerosols Affect Precipitation?

    E-Print Network [OSTI]

    Daniel, Rosenfeld

    Flood or Drought: How Do Aerosols Affect Precipitation? Daniel Rosenfeld,1 * Ulrike Lohmann,2 and the initiation of precipitation. Large concentrations of human-made aerosols have been reported to both decrease hand, heavily polluted clouds evaporate much of their water before precipitation can occur, if they can

  17. Impact of natural and anthropogenic aerosols on stratocumulus and precipitation in the Southeast Pacific: A regional modeling study using WRF-Chem

    SciTech Connect (OSTI)

    Yang, Qing; Gustafson, William I.; Fast, Jerome D.; Wang, Hailong; Easter, Richard C.; Wang, Minghuai; Ghan, Steven J.; Berg, Larry K.; Leung, Lai-Yung R.; Morrison, H.

    2012-09-28

    Cloud-system resolving simulations with the chemistry version of the Weather Research and Forecasting (WRF-Chem) model are used to quantify the impacts of regional anthropogenic and oceanic emissions on changes in aerosol properties, cloud macro- and microphysics, and cloud radiative forcing over the Southeast Pacific (SEP) during the VAMOS Ocean-Cloud-Atmosphere-Land Study Regional Experiment (VOCALS-REx) (15 Oct–Nov 16, 2008). The effects of oceanic aerosols on cloud properties, precipitation, and the shortwave forcing counteract those of anthropogenic aerosols. Despite the relatively small changes in Na concentrations (2-12%) from regional oceanic emissions, their net effect (direct and indirect) on the surface shortwave forcing is opposite and comparable or even larger in magnitude compared to those of regional anthropogenic emissions over the SEP. Two distinct regions are identified in the VOCALS-REx domain. The near-coast polluted region is characterized with strong droplet activation suppression of small particles by sea-salt particles, the more important role of the first than the second indirect effect, low surface precipitation rate, and low aerosol-cloud interaction strength associated with anthropogenic emissions. The relatively clean remote region is characterized with large contributions of Cloud Condensation Nuclei (CCN, number concentration denoted by NCCN) and droplet number concentrations (Nd) from non-local sources (lateral boundaries), a significant amount of surface precipitation, and high aerosol-cloud interactions under a scenario of five-fold increase in anthropogenic emissions. In the clean region, cloud properties have high sensitivity (e.g., 13% increase in cloud-top height and a 9% surface albedo increase) to the moderate increase in CCN concentration (?Nccn = 13 cm-3; 25%) produced by a five-fold increase in regional anthropogenic emissions. The increased anthropogenic aerosols reduce the precipitation amount over the relatively clean remote ocean. The reduction of precipitation (as a cloud water sink) more than doubles the wet scavenging timescale, resulting in an increased aerosol lifetime in the marine boundary layer. Therefore, the aerosol impacts on precipitation are amplified by the positive feedback of precipitation on aerosol. The positive feedback ultimately alters the cloud micro- and macro-properties, leading to strong aerosol-cloud-precipitation interactions. The higher sensitivity of clouds to anthropogenic aerosols over this region is also related to a 16% entrainment rate increase due to anthropogenic aerosols. The simulated aerosol-cloud-precipitation interactions are stronger at night over the clean marine region, while during the day, solar heating results in more frequent decoupling, thinner clouds, reduced precipitation, and reduced sensitivity to anthropogenic emissions. The simulated high sensitivity to the increased anthropogenic emissions over the clean region suggests that the perturbation of the clean marine environment with anthropogenic aerosols may have a larger effect on climate than that of already polluted marine environments.

  18. Experiments related to the resuspension of aerosols during hydrogen burns

    SciTech Connect (OSTI)

    Nelson, L.S.; Guay, K.P.

    1987-01-01

    We have performed seven ''add-on'' experiments in two large combustion facilities to investigate the capability of hydrogen burns to remove simulated structural and fission product aerosols previously deposited on small metal discs that have surfaces prototypical of those found in nuclear reactor containments. Our results suggest that hydrogen combustion provides an especially effective mechanism for removal (and, presumably, resuspension) of sedimented aerosols produced in a hypothetical nuclear reactor core-degradation or core-melting accident. The presence of condensing steam does not seem to assure adhesion of sedimented aerosols during hydrogen burns. Differences are exhibited between different surfaces as well as between types of aerosol. In-depth studies will be required to assess the impact exposure of sedimented aerosols to hydrogen burns might have on the radiological source term.

  19. Observations of Exoplanet Atmospheres

    E-Print Network [OSTI]

    Crossfield, Ian J M

    2015-01-01

    Detailed characterization of an extrasolar planet's atmosphere provides the best hope for distinguishing the makeup of its outer layers, and the only hope for understanding the interplay between initial composition, chemistry, dynamics & circulation, and disequilibrium processes. In recent years, some areas have seen rapid progress while developments in others have come more slowly and/or have been hotly contested. This article gives an observer's perspective on the current understanding of extrasolar planet atmospheres prior to the considerable advances expected from the next generation of observing facilities. Atmospheric processes of both transiting and directly-imaged planets are discussed, including molecular and atomic abundances, cloud properties, thermal structure, and planetary energy budgets. In the future we can expect a continuing and accelerating stream of new discoveries, which will fuel the ongoing exoplanet revolution for many years to come.

  20. Study of Aerosol Indirect Effects in China

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power AdministrationRobust,Field-effect PhotovoltaicsStructure andChallenge | Department,Aerosol Indirect Effects in

  1. Chemical distribution in high-solids paint overspray aerosols

    SciTech Connect (OSTI)

    D'Arcy, J.B.; Chan, T.L. )

    1990-03-01

    The chemical composition of high-solids basecoat paint overspray aerosols was determined as a function of particle size. Detailed information on the chemical composition of the overspray aerosols is important in health hazard evaluation since the composition and distribution within the airborne particles may differ significantly from the bulk paint material. This study was conducted in a typical down-draft paint booth equipped with air-atomized spray painting equipment. A fixed paint target was used to simulate typical overspray generation conditions and the aerosols were collected isokinetically with a seven-stage cascade impactor for size-fractionated analysis. The overspray aerosol from six paints consisted of organic paint binders with varying amounts of inorganic species as pigments or luster enhancers. These overspray aerosols had mass median aerodynamic diameters (MMAD) ranging from 2.9 to 9.7 microns. The size-fractionated paint samples collected on the impaction stages were analyzed by energy dispersive X-ray spectrometry on a scanning electron microscope (SEM-EDXRS) to identify the metallic elements. Atomic absorption spectrometry was used to determine the mass distribution of aluminum and iron as indicators of nonuniform distribution. Three of the aerosols containing aluminum were found to have bimodal distributions with most aluminum distributions having cumulative MMADs larger than the total aerosol. Iron in the aerosols was bimodal for three of the paints with all samples having an overall iron MMAD less than or equal to the overspray aerosol MMAD. Analysis using ultraviolet spectrometry revealed that the organic compounds present in the size-fractionated particulate samples consisted of a single, polydispersed mode with an MMAD similar to that of the total overspray aerosol.

  2. Seasonal and diurnal variations of submicron organic aerosol in Tokyo observed using the Aerodyne aerosol mass spectrometer

    E-Print Network [OSTI]

    Jimenez, Jose-Luis

    with carbon monoxide (CO) and fragments of aliphatic and oxygenated organic compounds in the AMS mass spectra. Combustion-related organic aerosol (combustion OA) is defined as the primary organic aerosol (POA) fraction the combustion OA and the background OA from the total OA. The combustion OA and excess OA show good correlation

  3. Single point aerosol sampling: Evaluation of mixing and probe performance in a nuclear stack

    SciTech Connect (OSTI)

    Rodgers, J.C.; Fairchild, C.I.; Wood, G.O.; Ortiz, C.A.; Muyshondt, A.

    1996-01-01

    Alternative reference methodologies have been developed for sampling of radionuclides from stacks and ducts, which differ from the methods previously required by the United States Environmental Protection Agency. These alternative reference methodologies have recently been approved by the U.S. EPA for use in lieu of the current standard techniques. The standard EPA methods are prescriptive in selection of sampling locations and in design of sampling probes whereas the alternative reference methodologies are performance driven. Tests were conducted in a stack at Los Alamos National Laboratory to demonstrate the efficacy of some aspects of the alternative reference methodologies. Coefficients of variation of velocity, tracer gas, and aerosol particle profiles were determined at three sampling locations. Results showed that numerical criteria placed upon the coefficients of variation by the alternative reference methodologies were met at sampling stations located 9 and 14 stack diameters from the flow entrance, but not at a location that was 1.5 diameters downstream from the inlet. Experiments were conducted to characterize the transmission of 10 {mu}m aerodynamic diameter liquid aerosol particles through three types of sampling probes. The transmission ratio (ratio of aerosol concentration at the probe exit plane to the concentration in the free stream) was 107% for a 113 L min{sup {minus}1} (4-cfm) anistokinetic shrouded probe, but only 20% for an isokinetic probe that follows the existing EPA standard requirements. A specially designed isokinetic probe showed a transmission ratio of 63%. The shrouded probe performance would conform to the alternative reference methodologies criteria; however, the isokinetic probes would not. 13 refs., 9 figs., 1 tab.

  4. Investigation of Aerosol Sources, Lifetime and Radiative Forcing through Multi-Instrument Data Assimilation

    E-Print Network [OSTI]

    Rubin, Juli Irene

    2012-01-01

    of the various radiative mechanims associated with aerosolof the various radiative mechanims associated with aerosol

  5. Analysis of reflectance spectra of UV-absorbing aerosol scenes measured by SCIAMACHY

    E-Print Network [OSTI]

    Graaf, Martin de

    Analysis of reflectance spectra of UV-absorbing aerosol scenes measured by SCIAMACHY M. de Graaf,1 of reflectance spectra of UV-absorbing aerosol scenes measured by SCIAMACHY, J. Geophys. Res., 112, D02206, doi aerosol (DDA) and biomass burning aerosol (BBA) scenes over oceans are presented, measured by the space

  6. Satellite observations of the seasonal cycles of absorbing aerosols in Africa

    E-Print Network [OSTI]

    Graaf, Martin de

    Satellite observations of the seasonal cycles of absorbing aerosols in Africa related to monsoon of aerosol emissions from the wet surface. 1. Introduction The main aerosol types occurring over Africa Africa can be characterized using Absorbing Aerosol Index (AAI) data from Global Ozone Monitoring

  7. Advances and applications of mass spectral techniques for the characterization of atmospheric aerosol particles

    E-Print Network [OSTI]

    Hatch, Lindsay Erighn

    2012-01-01

    characterization experiments utilized gas-phase analytes that were introduced by flowing nitrogen over a reservoir

  8. Carbonaceous aerosols are increasingly rec-ognized as an important atmospheric constituent.

    E-Print Network [OSTI]

    sunlight strongly and almost uniformly across the solar spectrum. However,the graphite seldom is pure with time; as,for example,with the transition from household stoves to less polluting central heating

  9. X-RAY METHODS FOR THE CHEMICAL CHARACTERIZATION OF ATMOSPHERIC AEROSOLS

    E-Print Network [OSTI]

    Jaklevic, J.M.

    2010-01-01

    for the routine analysis of air pollution samples, itof x-ray methods to the analysis of air particulate samples.

  10. ATMOSPHERIC AEROSOL SOURCE-RECEPTOR RELATIONSHIPS: THE ROLE OF COAL-FIRED POWER PLANTS

    SciTech Connect (OSTI)

    Allen L. Robinson; Spyros N. Pandis; Cliff I. Davidson

    2002-03-01

    This report describes the technical progress made on the Pittsburgh Air Quality Study (PAQS) during the period of August 2001 through January of 2002. The major activity during this project period was the continuation of the ambient monitoring effort. Work also progressed on organizing the upcoming source characterization effort, and there was continued development of several three-dimensional air quality models. The first PAQS data analysis workshop for the project was held at Carnegie Mellon in December 2001. Two new instruments were added to site during this project period: a single particle mass spectrometer and an in situ VOC instrument. The single particle mass spectrometer has been deployed since the middle of September and has collected more than 150 days of data. The VOC instrument was only deployed during the intensive sampling period. Several instruments experienced operational issues during this project period. The overall data recovery rate for the project has been high.

  11. Chemistry of atmospheric aerosol particles and their resulting warm cloud-nucleation properties

    E-Print Network [OSTI]

    Moore, Meagan Julia Kerry

    2011-01-01

    detection efficiency, Analytical Chemistry, 76, 712-719,Portable ATOFMS, Analytical Chemistry, 69, 4083-4091, 1997.Network, ART-2A, Analytical Chemistry, 71 (4), 860-865,

  12. The Evolution of the Physicochemical Properties of Aerosols in the Atmosphere 

    E-Print Network [OSTI]

    Tomlinson, Jason

    2011-02-22

    with an average kappa?between 0.01 and 0.05 for all dry particle diameters. Cloud condensation nuclei closure was attained at a supersaturation of 0.2 percent for all particles within the free troposphere by either assuming a pure ammonium bisulfate composition...

  13. EMSL Science Theme Advisory Panel Workshop - Atmospheric Aerosol Chemistry, Climate Change, and Air Quality

    SciTech Connect (OSTI)

    Baer, Donald R.; Finlayson-Pitts, Barbara J.; Allen, Heather C.; Bertram, Allan K.; Grassian, Vicki H.; Martin, Scot T.; Penner, Joyce E.; Prather, Kimberly; Rasch, Philip J.; Signorell, Ruth; Smith, James N.; Wyslouzil, Barbara; Ziemann, Paul; Dabdub, Donald; Furche, Filipp; Nizkorodov, Sergey; Tobias, Douglas J.; Laskin, Julia; Laskin, Alexander

    2013-07-01

    This report contains the workshop scope and recommendations from the workshop attendees in identifying scientific gaps in new particle formation, growth and properties of particles and reactions in and on particles as well as the laboratory-focused capabilities, field-deployable capabilities and modeling/theory tools along with linking of models to fundamental data.

  14. Chemical Bonding and Structural Information of Black Carbon Reference Materials and Individual Carbonaceous Atmospheric Aerosols

    E-Print Network [OSTI]

    Hopkins, Rebecca J.; Tivanski, Alexei V.; Marten, Bryan D.; Gilles, Mary K.

    2007-01-01

    A. (1998), Determination of chemical- structural changes inOptical, physical, and chemical properties of tar ballsE. (2001), Study on the chemical character of water soluble

  15. Advances and applications of mass spectral techniques for the characterization of atmospheric aerosol particles

    E-Print Network [OSTI]

    Hatch, Lindsay Erighn

    2012-01-01

    1 Isoprene (2-methyl-1,3-butadiene, C 5 H 8 ) is an abundant4 Isoprene (2-methyl-1,3-butadiene, C 5 H 8 ) is the most

  16. Advances and applications of mass spectral techniques for the characterization of atmospheric aerosol particles

    E-Print Network [OSTI]

    Hatch, Lindsay Erighn

    2012-01-01

    and biomass burning. Combustion-related emissions areBiomass burning emissions include similar components as combustion

  17. DETERMINATION OF CARBON IN ATMOSPHERIC AEROSOLS BY DEUTERON-INDUCED NUCLEAR REACTIONS

    E-Print Network [OSTI]

    Clemenson, Mark

    2013-01-01

    sensitive detection of the y radiation from the activationoverall detection coefficient for the annihilation radiationMeV annihilation radiation. The detection system is a Ge(Li)

  18. DETERMINATION OF LOW-Z ELEMENTS IN ATMOSPHERIC AEROSOLS BY CHARGED-PARTICLE-INDUCED NUCLEAR REACTIONS

    E-Print Network [OSTI]

    Clemenson, Mark Steven

    2013-01-01

    efficient for the detection of the radiation and because themost sensitive detection of gamma radiation from activationjust the detection of 0.511-MeV radiation the cheaper and

  19. ATMOSPHERIC AEROSOL RESEARCH FY-1979, CHAPTER IN THE ENERGY AND ENVIRONMENT ANNUAL REPORT, 1979

    E-Print Network [OSTI]

    Authors, Various

    2013-01-01

    1977), p. 249. the catalytic oxidation of S02 on carbon inand T. Novakov, "Catalytic oxidation of S02 on carbon inand mechanism for catalytic oxidation of S02 on carbon in

  20. Advances and applications of mass spectral techniques for the characterization of atmospheric aerosol particles

    E-Print Network [OSTI]

    Hatch, Lindsay Erighn

    2012-01-01

    86. Sullivan, A. P. ; Peltier, R. E. ; Brock, C. A. ; deD. R. ; Snyder, D. C. ; Peltier, R. E. ; Weber, R. J. ;A. G. ; Brock, C. A. ; Peltier, R. ; Sullivan, A. P. ;

  1. Experimental and theoretical investigation of nucleation and growth of atmospheric aerosols 

    E-Print Network [OSTI]

    Zhao, Jun

    2009-05-15

    of strong hydrogen bonding between an organic acid and sulfuric acid is likely responsible for a reduction of the nucleation barrier by modifying the hydrophobic properties of the organic acid and allowing further addition of hydrophilic species (e.g., H2SO4...

  2. DETERMINATION OF LOW-Z ELEMENTS IN ATMOSPHERIC AEROSOLS BY CHARGED-PARTICLE-INDUCED NUCLEAR REACTIONS

    E-Print Network [OSTI]

    Clemenson, Mark Steven

    2013-01-01

    of the target nuclide N0 =Avogadro's Number, 6.02 xlo- 2 3fractional abundance, and Avogadro's number, of course, will

  3. Carbon oxidation state as a metric for describing the chemistry of atmospheric organic aerosol

    E-Print Network [OSTI]

    Kroll, Jesse

    A detailed understanding of the sources, transformations and fates of organic species in the environment is crucial because of the central roles that they play in human health, biogeochemical cycles and the Earth's climate. ...

  4. ATMOSPHERIC AEROSOL RESEARCH FY-1979, CHAPTER IN THE ENERGY AND ENVIRONMENT ANNUAL REPORT, 1979

    E-Print Network [OSTI]

    Authors, Various

    2013-01-01

    been reproduced using coal fly ash samples, which have a lowH20 and acid washes on the fly- ash surface. Because ESCA isof the Ca species onto the fly- ash surface as leaching from

  5. Real time in situ detection of organic nitrates in atmospheric aerosols

    SciTech Connect (OSTI)

    Rollins, Andrew W.; Smith, Jared D.; Wilson, Kevin R.; Cohen, Ronald C.

    2010-06-11

    A new field instrument is described that quantifies total particle phase organic nitrates. The instrument is based on the thermal dissociation laser induced fluorescence (TD-LIF) method that thermally converts nitrates to NO2 which is then detected by LIF. This instrument is unique in its ability to provide fast sensitive measurements of particle phase organic nitrates, without interference from inorganic nitrate. Here we use it to quantify organic nitrates in SOA generated from high-NOx photooxidation of limonene, a-pinene, D-3-carene, and tridecane. In these experiments the organic nitrate moiety is observed to be 6-15percent of the total SOA mass, depending on the organic precursor.

  6. Atmospheric Aerosol Nucleation Shanhu Lee, Kent State University (http://www.personal.kent.edu/~slee19/)

    E-Print Network [OSTI]

    Lee, Shan-Hu

    pre- dicted rather low stabilities for HSO5 with respect to disso- ciation into SO3+HO2, and have, HSO5, SO3 and HO2, and also reanalyzed the individual steps of the HSO3+O2HSO5SO3+HO2 reaction

  7. ATMOSPHERIC AEROSOL RESEARCH FY-1979, CHAPTER IN THE ENERGY AND ENVIRONMENT ANNUAL REPORT, 1979

    E-Print Network [OSTI]

    Authors, Various

    2013-01-01

    XBL 801-45) Species found in leachate from flyash. Acid washinformation if the leachate is analyzed as a function ofand not be found in the leachate. Nevertheless, because

  8. Atmospheric Environment 40 (2006) 35363547 Long-range aerosol transport from Europe to Istanbul, Turkey

    E-Print Network [OSTI]

    Chen, Shu-Hua

    2006-01-01

    . Meteorological modeling provided the wind fields that were first used in a trajectory analysis and then, along. Istanbul is the largest urban settlement in Northwestern Turkey, with more than 12 million inhabitants with other meteorological data, input to an advanced air quality model. Backward trajectories suggested

  9. Scanning Transmission X-ray Microscopy: Applications in Atmospheric Aerosol Research

    E-Print Network [OSTI]

    Moffet, Ryan C.

    2011-01-01

    polymer photoresists by scanning transmission x-ray microscopy. Journal of Vacuum Science and Technology

  10. Method for Characterization of Low Molecular Weight Organic Acids in Atmospheric Aerosols Using Ion Chromatography Mass

    E-Print Network [OSTI]

    Dickerson, Russell R.

    Clean Air act as criteria pollutant particulate matter (PM). Although the Clean Air Act designates spectroscopy (FTIR), liquid chromatography with ultraviolet detection (LCUV), or nuclear magnetic resonance

  11. About ÂŤEffectiveÂŽ Height of the Aerosol Atmosphere in Visible and IR Wavelength Range

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity ofkandz-cm11 OutreachProductswsicloudwsicloudden Documentation DataStreamsTotalproposalsAbout SAGEAbout theAbout

  12. Posters Scanning Raman Lidar Measurements of Atmospheric Water Vapor and Aerosols

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration wouldMass mapSpeedingProgram Guidelines This document outlines the majorL.Posters955 Posters

  13. Global Aerosol Health Impacts: Quantifying Uncertainties

    E-Print Network [OSTI]

    Selin, Noelle E.

    Atmospheric fine particulate matter <2.5 ?m (PM2.5) can cause cardiovasculatory and respiratory damages and mortalities. Assessing population exposure to and damages from PM2.5 is important for policy, but measurement ...

  14. Autumn 2012 Atmospheric Circulation

    E-Print Network [OSTI]

    Doty, Sharon Lafferty

    wind, and accumulated precipitation at a designated city. Forecasts are made over a two-week period Department 1 The UW Atmospheric Sciences spring forecast contest has been an annual tradition there will be a marine push or a convergence zone wrecking their forecast for maximum temperature and precipitation

  15. Laboratory for Atmospheric and

    E-Print Network [OSTI]

    Mojzsis, Stephen J.

    Laboratory for Atmospheric and Space Physics Activity Report 2013 University of Colorado at Boulder from the Naval Research Center and the Air Force Cambridge Research Laboratory (now the Phillips Laboratory), the University of Colorado formed a research group called the Upper Air Laboratory (UAL

  16. Laboratory for Atmospheric and

    E-Print Network [OSTI]

    Mojzsis, Stephen J.

    Laboratory for Atmospheric and Space Physics Activity Report 2012 University of Colorado at Boulder from the Naval Research Center and the Air Force Cambridge Research Laboratory (now the Phillips Laboratory), the University of Colorado formed a research group called the Upper Air Laboratory (UAL

  17. Laboratory for Atmospheric and

    E-Print Network [OSTI]

    Mojzsis, Stephen J.

    Laboratory for Atmospheric and Space Physics Activity Report 2008 University of Colorado at Boulder, Jet Propulsion Laboratory) LASP: A Brief History In 1946-47, a handful of American universities joined Laboratory (now the Phillips Laboratory), the University of Colorado formed a research group called the Upper

  18. Laboratory for Atmospheric and

    E-Print Network [OSTI]

    Mojzsis, Stephen J.

    1 Laboratory for Atmospheric and Space Physics Activity Report 2010 University of Colorado from the Na- val Research Center and the Air Force Cambridge Research Laboratory (now the Phillips Laboratory), the University of Colorado formed a research group called the Upper Air Laboratory (UAL

  19. ATMOSPHERIC CHEMISTRY AND PHYSICS

    E-Print Network [OSTI]

    Brandenburg, Axel

    of electronic formats. Some content that appears in print may not be available in electronic formats. For more information about Wiley products, visit our web site at www.wiley.com. Library of Congress Cataloging components of the atmosphere, nitrogen, oxygen, water, carbon dioxide, and the noble gases. In the late

  20. Asthmatic responses to airborne acid aerosols

    SciTech Connect (OSTI)

    Ostro, B.D.; Lipsett, M.J.; Wiener, M.B.; Selner, J.C. )

    1991-06-01

    Controlled exposure studies suggest that asthmatics may be more sensitive to the respiratory effects of acidic aerosols than individuals without asthma. This study investigates whether acidic aerosols and other air pollutants are associated with respiratory symptoms in free-living asthmatics. Daily concentrations of hydrogen ion (H+), nitric acid, fine particulates, sulfates and nitrates were obtained during an intensive air monitoring effort in Denver, Colorado, in the winter of 1987-88. A panel of 207 asthmatics recorded respiratory symptoms, frequency of medication use, and related information in daily diaries. We used a multiple regression time-series model to analyze which air pollutants, if any, were associated with health outcomes reported by study participants. Airborne H+ was found to be significantly associated with several indicators of asthma status, including moderate or severe cough and shortness of breath. Cough was also associated with fine particulates, and shortness of breath with sulfates. Incorporating the participants' time spent outside and exercise intensity into the daily measure of exposure strengthened the association between these pollutants and asthmatic symptoms. Nitric acid and nitrates were not significantly associated with any respiratory symptom analyzed. In this population of asthmatics, several outdoor air pollutants, particularly airborne acidity, were associated with daily respiratory symptoms.

  1. Molecular marker analysis as a guide to the sources of fine organic aerosols

    SciTech Connect (OSTI)

    Rogge, W.F.; Cass, G.R.; Hildemann, L.M.; Mazurek, M.A.; Simoneit, B.R.T.

    1992-07-01

    The molecular composition of fine particulate (D{sub p} {ge} 2 {mu}m) organic aerosol emissions from the most important sources in the Los Angeles area has been determined. Likewise, ambient concentration patterns for more than 80 single organic compounds have been measured at four urban sites (West Los Angeles, Downtown Los Angeles, Pasadena, and Rubidoux) and at one remote offshore site (San Nicolas Island). It has been found that cholesterol serves as a marker compound for emissions from charbroilers and other meat cooking operations. Vehicular exhaust being emitted from diesel and gasoline powered engines can be traced in the Los Angeles atmosphere using fossil petroleum marker compounds such as steranes and pentacyclic triterpanes (e.g., hopanes). Biogenic fine particle emission sources such as plant fragments abraded from leaf surfaces by wind and weather can be traced in the urban atmosphere. Using distinct and specific source organic tracers or assemblages of organic compounds characteristic for the sources considered it is possible to estimate the influence of different source types at any urban site where atmospheric data are available.

  2. Molecular marker analysis as a guide to the sources of fine organic aerosols

    SciTech Connect (OSTI)

    Rogge, W.F.; Cass, G.R. ); Hildemann, L.M. . Dept. of Civil Engineering); Mazurek, M.A. ); Simoneit, B.R.T. Environmental Geochemistry Group)

    1992-07-01

    The molecular composition of fine particulate (D[sub p] [ge] 2 [mu]m) organic aerosol emissions from the most important sources in the Los Angeles area has been determined. Likewise, ambient concentration patterns for more than 80 single organic compounds have been measured at four urban sites (West Los Angeles, Downtown Los Angeles, Pasadena, and Rubidoux) and at one remote offshore site (San Nicolas Island). It has been found that cholesterol serves as a marker compound for emissions from charbroilers and other meat cooking operations. Vehicular exhaust being emitted from diesel and gasoline powered engines can be traced in the Los Angeles atmosphere using fossil petroleum marker compounds such as steranes and pentacyclic triterpanes (e.g., hopanes). Biogenic fine particle emission sources such as plant fragments abraded from leaf surfaces by wind and weather can be traced in the urban atmosphere. Using distinct and specific source organic tracers or assemblages of organic compounds characteristic for the sources considered it is possible to estimate the influence of different source types at any urban site where atmospheric data are available.

  3. Human health benefits of ambient sulfate aerosol reductions under Title IV of the 1990 Clean Air Act amendments

    SciTech Connect (OSTI)

    Chestnut, L.G. [Hagler Bailly Consulting, Inc., Boulder, CO (United States); Watkins, A.M. [Environmental Protection Agency, Washington, DC (United States)

    1997-12-31

    The Acid Rain Provisions (Title IV) of the Clean Air Act Amendments of 1990 call for about a 10 million ton reduction in annual SO{sub 2} emissions in the United States by the year 2010. Although the provisions apply nationwide, most of the reduction will take place in the eastern half of the United States, where use of high sulfur coal for electricity generation is most common. One potentially large benefit of Title IV is the expected reduction in adverse human health effects associated with exposure to ambient sulfate aerosols, a secondary pollutant formed in the atmosphere when SO{sub 2} is present. Sulfate aerosols are a significant constituent of fine particulate (PM{sub 2.5}). This paper combines available epidemiologic evidence of health effects associated with sulfate aerosols and economic estimates of willingness to pay for reductions in risks or incidence of health effects with available estimates of the difference between expected ambient sulfate concentrations in the eastern United States and southeastern Canada with and without Title IV to estimate the expected health benefits of Title IV. The results suggest a mean annual benefit in the eastern United States of $10.6 billion (in 1994 dollars) in 1997 and $40.0 billion in 2010, with an additional $1 billion benefit each year in Ontario and Quebec provinces.

  4. ATMOSPHERIC SCIENCES Observations from

    E-Print Network [OSTI]

    Pierce, Stephen

    samples from the recovery cruise and Bob O'Malley for evaluation of the CTD sensors used on the deployment p. 8 b. Instrument Calibration p. 9 Ocean Temperature and Salinity Sensors p. 9 Met Sensors p. 10 Doppler Profiler Compass p. 10 ADCP/ADP Battery Capacity p. 11 Pressure Sensors p. 11 CTD Sensors p. 12 c

  5. EIA - State Nuclear Profiles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration would like submitKansas Nuclear Profile 2010 Kansas profile Kansas total electric power

  6. EIA - State Nuclear Profiles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration would like submitKansas Nuclear Profile 2010 Kansas profile Kansas total electric powerLouisiana

  7. EIA - State Nuclear Profiles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration would like submitKansas Nuclear Profile 2010 Kansas profile Kansas total electric

  8. EIA - State Nuclear Profiles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration would like submitKansas Nuclear Profile 2010 Kansas profile Kansas total electricMassachusetts

  9. EIA - State Nuclear Profiles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration would like submitKansas Nuclear Profile 2010 Kansas profile Kansas totalMinnesota Nuclear

  10. EIA - State Nuclear Profiles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration would like submitKansas Nuclear Profile 2010 Kansas profile Kansas totalMinnesota

  11. EIA - State Nuclear Profiles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration would like submitKansas Nuclear Profile 2010 Kansas profile Kansas totalMinnesotaMissouri

  12. EIA - State Nuclear Profiles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration would like submitKansas Nuclear Profile 2010 Kansas profile KansasHampshire Nuclear

  13. EIA - State Nuclear Profiles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration would like submitKansas Nuclear Profile 2010 Kansas profile KansasHampshire NuclearOhio Nuclear

  14. EIA - State Nuclear Profiles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration would like submitKansas Nuclear Profile 2010 Kansas profile KansasHampshire NuclearOhio

  15. EIA - State Nuclear Profiles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration would like submitKansas Nuclear Profile 2010 Kansas profile KansasHampshire NuclearOhioSouth

  16. EIA - State Nuclear Profiles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration would like submitKansas Nuclear Profile 2010 Kansas profile KansasHampshire

  17. EIA - State Nuclear Profiles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration would like submitKansas Nuclear Profile 2010 Kansas profile KansasHampshireTexas

  18. EIA - State Nuclear Profiles

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration would like submitKansas Nuclear Profile 2010 Kansas profile KansasHampshireTexasWisconsin

  19. Fire aerosol experiment and comparisons with computer code predictions

    SciTech Connect (OSTI)

    Gregory, W.S.; Nichols, B.D.; White, B.W.; Smith, P.R.; Leslie, I.H.; Corkran, J.R.

    1988-01-01

    Los Alamos National Laboratory, in cooperation with New Mexico State University, has carried on a series of tests to provide experimental data on fire-generated aerosol transport. These data will be used to verify the aerosol transport capabilities of the FIRAC computer code. FIRAC was developed by Los Alamos for the US Nuclear Regulatory Commission. It is intended to be used by safety analysts to evaluate the effects of hypothetical fires on nuclear plants. One of the most significant aspects of this analysis deals with smoke and radioactive material movement throughout the plant. The tests have been carried out using an industrial furnace that can generate gas temperatures to 300/degree/C. To date, we have used quartz aerosol with a median diameter of about 10 ..mu..m as the fire aerosol simulant. We also plan to use fire-generated aerosols of polystyrene and polymethyl methacrylate (PMMA). The test variables include two nominal gas flow rates (150 and 300 ft/sup 3//min) and three nominal gas temperatures (ambient, 150/degree/C, and 300/degree/C). The test results are presented in the form of plots of aerosol deposition vs length of duct. In addition, the mass of aerosol caught in a high-efficiency particulate air (HEPA) filter during the tests is reported. The tests are simulated with the FIRAC code, and the results are compared with the experimental data. 3 refs., 10 figs., 1 tab.

  20. Implementing marine organic aerosols into the GEOS-Chem model

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Gantt, B.; Johnson, M. S.; Crippa, M.; Prévôt, A. S. H.; Meskhidze, N.

    2015-03-17

    Marine-sourced organic aerosols (MOAs) have been shown to play an important role in tropospheric chemistry by impacting surface mass, cloud condensation nuclei, and ice nuclei concentrations over remote marine and coastal regions. In this work, an online marine primary organic aerosol emission parameterization, designed to be used for both global and regional models, was implemented into the GEOS-Chem (Global Earth Observing System Chemistry) model. The implemented emission scheme improved the large underprediction of organic aerosol concentrations in clean marine regions (normalized mean bias decreases from -79% when using the default settings to -12% when marine organic aerosols are added). Modelmore »predictions were also in good agreement (correlation coefficient of 0.62 and normalized mean bias of -36%) with hourly surface concentrations of MOAs observed during the summertime at an inland site near Paris, France. Our study shows that MOAs have weaker coastal-to-inland concentration gradients than sea-salt aerosols, leading to several inland European cities having >10% of their surface submicron organic aerosol mass concentration with a marine source. The addition of MOA tracers to GEOS-Chem enabled us to identify the regions with large contributions of freshly emitted or aged aerosol having distinct physicochemical properties, potentially indicating optimal locations for future field studies.« less