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Note: This page contains sample records for the topic "aerosols atmospheric profiling" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


1

Atmospheric Aerosol Systems | EMSL  

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

Science Themes Atmospheric Aerosol Systems Overview Atmospheric Aerosol Systems Biosystem Dynamics & Design Energy Materials & Processes Terrestrial & Subsurface Ecosystems...

2

Turn-key Raman lidar for profiling atmospheric water vapor, clouds, and aerosols at the US Southern Great Plains Climate Study Site  

SciTech Connect (OSTI)

There are clearly identified scientific requirements for continuous profiling of atmospheric water vapor at the Department of Energy, Atmospheric Radiation Measurement program, Southern Great Plains CART (Cloud and Radiation Testbed) site in northern Oklahoma. Research conducted at several laboratories has demonstrated the suitability of Raman lidar for providing measurements that are an excellent match to those requirements. We have developed and installed a ruggedized Raman lidar system that resides permanently at the CART site, and that is computer automated to eliminate the requirements for operator interaction. In addition to the design goal of profiling water vapor through most of the troposphere during nighttime and through the boundary layer during daytime, the lidar provides quantitative characterizations of aerosols and clouds, including depolarization measurements for particle phase studies.

Goldsmith, J.E.M.; Blair, F.H.; Bisson, S.E.

1997-12-31T23:59:59.000Z

3

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)]

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

Sivaraman, Chitra; Flynn, Connor

4

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)]

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

Newsom, Rob; Goldsmith, John

5

Atmospheric Aerosol Systems | EMSL  

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary)morphinanInformation InInformationCenterResearch HighlightsTools PrintableCARIBU ProposalBeamAtmospheric

6

DOE research on atmospheric aerosols  

SciTech Connect (OSTI)

Atmospheric aerosols are the subject of a significant component of research within DOE`s environmental research activities, mainly under two programs within the Department`s Environmental Sciences Division, the Atmospheric Radiation Measurement (ARM) Program and the Atmospheric Chemistry Program (ACP). Research activities conducted under these programs include laboratory experiments, field measurements, and theoretical and modeling studies. The objectives and scope of these programs are briefly summarized. The ARM Program is the Department`s major research activity focusing on atmospheric processes pertinent to understanding global climate and developing the capability of predicting global climate change in response to energy related activities. The ARM approach consists mainly of testing and improving models using long-term measurements of atmospheric radiation and controlling variables at highly instrumented sites in north central Oklahoma, in the Tropical Western Pacific, and on the North Slope of Alaska. Atmospheric chemistry research within DOE addresses primarily the issue of atmospheric response to emissions from energy-generation sources. As such this program deals with the broad topic known commonly as the atmospheric source-receptor sequence. This sequence consists of all aspects of energy-related pollutants from the time they are emitted from their sources to the time they are redeposited at the Earth`s surface.

Schwartz, S.E.

1995-11-01T23:59:59.000Z

7

Comparative Analysis of Urban Atmospheric Aerosol by Particle...  

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

Analysis of Urban Atmospheric Aerosol by Particle-Induced X-ray Emission (PIXE), Proton Elastic Scattering Analysis Comparative Analysis of Urban Atmospheric Aerosol by...

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)]

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

Sivaraman, Chitra; Flynn, Connor

9

atmospheric aerosols basic: Topics by E-print Network  

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

of atmospheric aerosol. Aplin, KL 2012-01-01 13 1. Introduction The atmospheric greenhouse effect is the basic mechanism Environmental Sciences and Ecology Websites Summary: 1....

10

Upper Atmospheric Density Profiles  

E-Print Network [OSTI]

· Uncertainties in aerodynamics, problems with signals from shaking solar panel, rotation of instrument about · Change in latitude per unit change in longitude along profile set by orbit inclination and latitude (not engineering) instrument, very high sensitivity, unseen part of 11-yr solar cycle · Current science

Withers, Paul

11

E-Print Network 3.0 - atmospheric aerosol size Sample Search...  

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

for about ten percent of all aerosols in the atmosphere. We... , can actually absorb solar energy and warm the atmosphere. Atmospheric aerosols are very important... by...

12

Vapor scavenging by atmospheric aerosol particles  

SciTech Connect (OSTI)

Particle growth due to vapor scavenging was studied using both experimental and computational techniques. Vapor scavenging by particles is an important physical process in the atmosphere because it can result in changes to particle properties (e.g., size, shape, composition, and activity) and, thus, influence atmospheric phenomena in which particles play a role, such as cloud formation and long range transport. The influence of organic vapor on the evolution of a particle mass size distribution was investigated using a modified version of MAEROS (a multicomponent aerosol dynamics code). The modeling study attempted to identify the sources of organic aerosol observed by Novakov and Penner (1993) in a field study in Puerto Rico. Experimentally, vapor scavenging and particle growth were investigated using two techniques. The influence of the presence of organic vapor on the particle`s hydroscopicity was investigated using an electrodynamic balance. The charge on a particle was investigated theoretically and experimentally. A prototype apparatus--the refractive index thermal diffusion chamber (RITDC)--was developed to study multiple particles in the same environment at the same time.

Andrews, E.

1996-05-01T23:59:59.000Z

13

Nonequilibrium Atmospheric Secondary Organic Aerosol Formation...  

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

Aerosol Formation and Growth. Abstract: Airborne particles play a critical role in air quality, human health effects, visibility and climate. Secondary organic aerosols (SOA)...

14

Raman lidar profiling of water vapor and aerosols over the ARM SGP Site  

SciTech Connect (OSTI)

The authors have developed and implemented automated algorithms to retrieve profiles of water vapor mixing ratio, aerosol backscattering, and aerosol extinction from Southern Great Plains (SGP) Cloud and Radiation Testbed (CART) Raman Lidar data acquired during both daytime and nighttime operations. The Raman lidar sytem is unique in that it is turnkey, automated system designed for unattended, around-the-clock profiling of water vapor and aerosols. These Raman lidar profiles are important for determining the clear-sky radiative flux, as well as for validating the retrieval algorithms associated with satellite sensors. Accurate, high spatial and temporal resolution profiles of water vapor are also required for assimilation into mesoscale models to improve weather forecasts. The authors have also developed and implemented routines to simultaneously retrieve profiles of relative humidity. These routines utilize the water vapor mixing ratio profiles derived from the Raman lidar measurements together with temperature profiles derived from a physical retrieval algorithm that uses data from a collocated Atmospheric Emitted Radiance Interferometer (AERI) and the Geostationary Operational Environmental Satellite (GOES). These aerosol and water vapor profiles (Raman lidar) and temperature profiles (AERI+GOES) have been combined into a single product that takes advantage of both active and passive remote sensors to characterize the clear sky atmospheric state above the CART site.

Ferrare, R.A.

2000-01-09T23:59:59.000Z

15

RAMAN LIDAR PROFILING OF WATER VAPOR AND AEROSOLS OVER THE ARM SGP SITE.  

SciTech Connect (OSTI)

We have developed and implemented automated algorithms to retrieve profiles of water vapor mixing ratio, aerosol backscattering, and aerosol extinction from Southern Great Plains (SGP) Cloud and Radiation Testbed (CART) Raman Lidar data acquired during both daytime and nighttime operations. This Raman lidar system is unique in that it is turnkey, automated system designed for unattended, around-the-clock profiling of water vapor and aerosols (Goldsmith et al., 1998). These Raman lidar profiles are important for determining the clear-sky radiative flux, as well as for validating the retrieval algorithms associated with satellite sensors. Accurate, high spatial and temporal resolution profiles of water vapor are also required for assimilation into mesoscale models to improve weather forecasts. We have also developed and implemented routines to simultaneously retrieve profiles of relative humidity. These routines utilize the water vapor mixing ratio profiles derived from the Raman lidar measurements together with temperature profiles derived from a physical retrieval algorithm that uses data from a collocated Atmospheric Emitted Radiance Interferometer (AERI) and the Geostationary Operational Environmental Satellite (GOES) (Feltz et al., 1998; Turner et al., 1999). These aerosol and water vapor profiles (Raman lidar) and temperature profiles (AERI+GOES) have been combined into a single product that takes advantage of both active and passive remote sensors to characterize the clear sky atmospheric state above the CART site.

FERRARE,R.A.

2000-01-09T23:59:59.000Z

16

The effect of aerosol vertical profiles on satellite-estimated surface particle sulfate concentrations  

SciTech Connect (OSTI)

The aerosol vertical distribution is an important factor in determining the relationship between satellite retrieved aerosol optical depth (AOD) and ground-level fine particle pollution concentrations. We evaluate how aerosol profiles measured by ground-based lidar and simulated by models can help improve the association between AOD retrieved by the Multi-angle Imaging Spectroradiometer (MISR) and fine particle sulfate (SO4) concentrations using matched data at two lidar sites. At the Goddard Space Flight Center (GSFC) site, both lidar and model aerosol profiles marginally improve the association between SO4 concentrations and MISR fractional AODs, as the correlation coefficient between cross-validation (CV) and observed SO4 concentrations changes from 0.87 for the no-scaling model to 0.88 for models scaled with aerosol vertical profiles. At the GSFC site, a large amount of urban aerosols resides in the well-mixed boundary layer so the column fractional AODs are already excellent indicators of ground-level particle pollution. In contrast, at the Atmospheric Radiation Measurement Program (ARM) site with relatively low aerosol loadings, scaling substantially improves model performance. The correlation coefficient between CV and observed SO4 concentrations is increased from 0.58 for the no-scaling model to 0.76 in the GEOS-Chem scaling model, and the model bias is reduced from 17% to 9%. In summary, despite the inaccuracy due to the coarse horizontal resolution and the challenges of simulating turbulent mixing in the boundary layer, GEOS-Chem simulated aerosol profiles can still improve methods for estimating surface aerosol (SO4) mass from satellite-based AODs, particularly in rural areas where aerosols in the free troposphere and any long-range transport of aerosols can significantly contribute to the column AOD.

Liu, Yang; Wang, Zifeng; Wang, Jun; Ferrare, Richard A.; Newsom, Rob K.; Welton, Ellsworth J.

2011-02-15T23:59:59.000Z

17

Composition and Reactions of Atmospheric Aerosol Particles  

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

Source type and mechanism information for the four aerosol samples gathered from the Caribbean, the Sea of Japan, and New Jersey. One way to gauge an aerosol's ability to stay...

18

AT631, Spring 2011 Introduction to Atmospheric Aerosols  

E-Print Network [OSTI]

. Pandis, Atmospheric Chemistry and Physics: From Air Pollution to Climate Change, Wiley-Interscience, 2006AT631, Spring 2011 Introduction to Atmospheric Aerosols Tuesdays 9-9:50 AM, 212B ACRC Wednesdays, Lab, 1-4 PM, ACB 10 Instructor: Prof. Sonia Kreidenweis Atmospheric Chemistry Bldg., Room 19 491

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)]

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

Newsom, Rob; Goldsmith, John

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)]

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

Sivaraman, Chitra; Flynn, Connor

Note: This page contains sample records for the topic "aerosols atmospheric profiling" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


21

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)]

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

Sivaraman, Chitra; Flynn, Connor

22

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)]

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

Sivaraman, Chitra; Flynn, Connor

23

atmospheric aerosol limb: Topics by E-print Network  

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

coefficient is 0.5 and then 1.0 2. For the same conditions calculate the H Weber, Rodney 5 Secondary organic aerosol 1. Atmospheric chemical mechanism for production...

24

atmospheric aerosols recorded: Topics by E-print Network  

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

coefficient is 0.5 and then 1.0 2. For the same conditions calculate the H Weber, Rodney 4 Secondary organic aerosol 1. Atmospheric chemical mechanism for production...

25

atmospheric aerosols relation: Topics by E-print Network  

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

coefficient is 0.5 and then 1.0 2. For the same conditions calculate the H Weber, Rodney 4 Secondary organic aerosol 1. Atmospheric chemical mechanism for production...

26

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

E-Print Network [OSTI]

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...

Glen, Crystal

2012-02-14T23:59:59.000Z

27

Diesel Aerosol Sampling in the Atmosphere  

SciTech Connect (OSTI)

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.

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

2000-06-19T23:59:59.000Z

28

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)]

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

Sivaraman, Chitra; Flynn, Connor

29

Cloud and Aerosol Properties, Precipitable Water, and Profiles of Temperature and Water Vapor from MODIS  

E-Print Network [OSTI]

Cloud and Aerosol Properties, Precipitable Water, and Profiles of Temperature and Water Vapor from such as cloud mask, atmos- pheric profiles, aerosol properties, total precipitable water, and cloud properties vapor amount, aerosol particles, and the subsequently formed clouds [9]. Barnes et al. [2] provide

Sheridan, Jennifer

30

Unintended consequences of atmospheric injection of sulphate aerosols.  

SciTech Connect (OSTI)

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.

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

2010-10-01T23:59:59.000Z

31

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth (AOD)ProductssondeadjustsondeadjustAboutScience Program Cumulus Humilis Aerosol Processing Study (CHAPS)

32

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation ProposedUsing Zirconia Nanoparticles asSecond stage of theEMI SIG

33

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed New SubstationCleanCommunity Involvement andMISR, and4ComplianceCW 2013

34

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed New SubstationCleanCommunity Involvement andMISR, and4ComplianceCW 2013Composition

35

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed New SubstationCleanCommunity Involvement andMISR, and4ComplianceCW

36

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed New SubstationCleanCommunity Involvement andMISR, and4ComplianceCWComposition and

37

E-Print Network 3.0 - atmospheric aerosol aggregates Sample Search...  

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

are also directly associated with reduction in visibility and with long-range transport... for atmospheric aerosols is their association ... Source: Brookhaven National...

38

E-Print Network 3.0 - atmospheric aerosol optical Sample Search...  

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

as a consequence of industrial activities. These aerosols enhance reflection of solar radiation by the earth-atmosphere... , Pittsburgh, PA, 1995. Loadings of ... Source:...

39

E-Print Network 3.0 - atmospheric aerosol characterisation Sample...  

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

October 4, 2004 Abstract Atmospheric aerosol particles scatter and absorb shortwave (solar) radiation and... of the U.S. Department of Energy under Contract No....

40

E-Print Network 3.0 - aerosols influencing atmospheric Sample...  

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

October 4, 2004 Abstract Atmospheric aerosol particles scatter and absorb shortwave (solar) radiation and... influencing cloud reflectance and precipitation formation. The...

Note: This page contains sample records for the topic "aerosols atmospheric profiling" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


41

E-Print Network 3.0 - atmospheric aerosol properties Sample Search...  

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

October 4, 2004 Abstract Atmospheric aerosol particles scatter and absorb shortwave (solar) radiation and... the industrial period, largely on account of uncertainties in the...

42

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

E-Print Network [OSTI]

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 ...

Steele, Henry Donnan, 1974-

2004-01-01T23:59:59.000Z

43

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

E-Print Network [OSTI]

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 ...

Kessler, Sean Herbert

2013-01-01T23:59:59.000Z

44

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)]

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

Newsom, Rob; Goldsmith, John

45

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

E-Print Network [OSTI]

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 ...

Johnson, Kirsten S. (Kirsten Sue)

2008-01-01T23:59:59.000Z

46

atmospheric aerosol source-receptor: Topics by E-print Network  

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

coefficient is 0.5 and then 1.0 2. For the same conditions calculate the H Weber, Rodney 6 Secondary organic aerosol 1. Atmospheric chemical mechanism for production...

47

DETERMINATION OF LOW-Z ELEMENTS IN ATMOSPHERIC AEROSOLS BY CHARGED-PARTICLE-INDUCED NUCLEAR REACTIONS  

E-Print Network [OSTI]

the nuclear reaction N14 (p,a)c 11 with low-energy protonsLOW-Z ELEMENTS IN ATMOSPHERIC AEROSOLS BY CHARGED-PARTICLE-INDUCED NUCLEAR REACTIONS Mark Steven Clemenson Energy

Clemenson, Mark Steven

2013-01-01T23:59:59.000Z

48

Scanning Transmission X-ray Microscopy: Applications in Atmospheric Aerosol Research  

SciTech Connect (OSTI)

Scanning transmission x-ray microscopy (STXM) combines x-ray microscopy and near edge x-ray absorption fine structure spectroscopy (NEXAFS). This combination provides spatially resolved bonding and oxidation state information. While there are reviews relevant to STXM/NEXAFS applications in other environmental fields (and magnetic materials) this chapter focuses on atmospheric aerosols. It provides an introduction to this technique in a manner approachable to non-experts. It begins with relevant background information on synchrotron radiation sources and a description of NEXAFS spectroscopy. The bulk of the chapter provides a survey of STXM/NEXAFS aerosol studies and is organized according to the type of aerosol investigated. The purpose is to illustrate the current range and recent growth of scientific investigations employing STXM-NEXAFS to probe atmospheric aerosol morphology, surface coatings, mixing states, and atmospheric processing.

Moffet, Ryan C.; Tivanski, Alexei V.; Gilles, Mary K.

2011-01-20T23:59:59.000Z

49

Impact of Aerosols on Atmospheric Attenuation Loss in Central Receiver Systems: Preprint  

SciTech Connect (OSTI)

Atmospheric attenuation loss between the heliostat field and receiver has been recognized as a significant source of loss in Central Receiver Systems. In clear sky situations, extinction of Direct Normal Irradiance (DNI) is primarily by aerosols in the atmosphere. When aerosol loading is high close to the surface the attenuation loss between heliostat and receivers is significantly influenced by the amount of aerosols present on a particular day. This study relates measured DNI to aerosol optical depths close to the surface of the earth. The model developed in the paper uses only measured DNI to estimate the attenuation between heliostat and receiver in a central receiver system. The requirement that only a DNI measurement is available potentially makes the model a candidate for widespread use.

Sengupta, M.; Wagner, M. J.

2011-08-01T23:59:59.000Z

50

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

E-Print Network [OSTI]

Pacific Northwest National Laboratory POAs Primary Organic Aerosols SEMARNAT Secretaria del Medio Ambiente Recursos Naturales SHARP Study of Houston Atmospheric Radical Precursors SSA Single Scattering Albedo SOAs Secondary Organic Aerosols... quality and climate. Historically, the region has exceeded both the US EPA National Ambient Air Quality (NAAQS) and Mexico?s Secretaria del Medio Ambiente Recursos Naturales (SEMARNAT) air standards, stimulating a united interest. When comparing...

Levy, Misti E

2013-04-29T23:59:59.000Z

51

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 Union 2007 Joint Assembly Acapulco, Mexico May 22-25, 2007 Environmental Sciences Department Research Observations (MILAGRO) /Megacity Aerosol Experiment in Mexico City (MAX

52

Measurements of aerosol vertical profiles and optical properties during INDOEX  

E-Print Network [OSTI]

Markowicz,5 James R. Campbell,6 James D. Spinhirne,7 Howard R. Gordon,2 and James E. Johnson3 Received 5 field phase. Measurements were made from two platforms: the NOAA ship R/V Ronald H. Brown. Markowicz, J. R. Campbell, J. D. Spinhirne, H. R. Gordon, and J. E. Johnson, Measurements of aerosol

53

Carbon oxidation state as a metric for describing the chemistry of atmospheric organic aerosol  

SciTech Connect (OSTI)

A detailed understanding of the sources, transformations, and fates of organic species in the environment is crucial because of the central roles that organics play in human health, biogeochemical cycles, and Earth's climate. However, such an understanding is hindered by the immense chemical complexity of environmental mixtures of organics; for example, atmospheric organic aerosol consists of at least thousands of individual compounds, all of which likely evolve chemically over their atmospheric lifetimes. Here we demonstrate the utility of describing organic aerosol (and other complex organic mixtures) in terms of average carbon oxidation state (OSC), a quantity that always increases with oxidation, and is readily measured using state-of-the-art analytical techniques. Field and laboratory measurements of OSC , using several such techniques, constrain the chemical properties of the organics and demonstrate that the formation and evolution of organic aerosol involves simultaneous changes to both carbon oxidation state and carbon number (nC).

Massachusetts Institute of Technology; Kroll, Jesse H.; Donahue, Neil M.; Jimenez, Jose L.; Kessler, Sean H.; Canagaratna, Manjula R.; Wilson, Kevin R.; Altieri, Katye E.; Mazzoleni, Lynn R.; Wozniak, Andrew S.; Bluhm, Hendrik; Mysak, Erin R.; Smith, Jared D.; Kolb, Charles E.; Worsnop, Douglas R.

2010-11-05T23:59:59.000Z

54

The importance of aerosol composition and mixing state on predicted CCN concentration and the variation of the importance with atmospheric processing of aerosol  

SciTech Connect (OSTI)

The influences of atmospheric aerosols on cloud properties (i.e., aerosol indirect effects) strongly depend on the aerosol CCN concentrations, which can be effectively predicted from detailed aerosol size distribution, mixing state, and chemical composition using Khler theory. However, atmospheric aerosols are complex and heterogeneous mixtures of a large number of species that cannot be individually simulated in global or regional models due to computational constraints. Furthermore, the thermodynamic properties or even the molecular identities of many organic species present in ambient aerosols are often not known to predict their cloud-activation behavior using Khler theory. As a result, simplified presentations of aerosol composition and mixing state are necessary for large-scale models. In this study, aerosol microphysics, CCN concentrations, and chemical composition measured at the T0 urban super-site in Mexico City during MILAGRO are analyzed. During the campaign in March 2006, aerosol size distribution and composition often showed strong diurnal variation as a result of both primary emissions and aging of aerosols through coagulation and local photochemical production of secondary aerosol species. The submicron aerosol composition was ~1/2 organic species. Closure analysis is first carried out by comparing CCN concentrations calculated from the measured aerosol size distribution, mixing state, and chemical composition using extended Khler theory to concurrent CCN measurements at five supersaturations ranging from 0.11% to 0.35%. The closure agreement and its diurnal variation are studied. CCN concentrations are also derived using various simplifications of the measured aerosol mixing state and chemical composition. The biases associated with these simplifications are compared for different supersaturations, and the variation of the biases is examined as a function of aerosol age. The results show that the simplification of internally mixed, size-independent particle composition leads to substantial overestimation of CCN concentration for freshly emitted aerosols in early morning, but can reasonably predict the CCN concentration after the aerosols underwent atmospheric processing for several hours. This analysis employing various simplifications provides insights into the essential information of particle chemical composition that needs to be represented in models to adequately predict CCN concentration and cloud microphysics.

Wang, J.; Cubison, M.; Aiken, A.; Jimenez, J.; Collins, D.; Gaffney, J.; Marley, N.

2010-03-15T23:59:59.000Z

55

Method for Characterization of Low Molecular Weight Organic Acids in Atmospheric Aerosols Using Ion Chromatography Mass  

E-Print Network [OSTI]

spectrometry (ESI-MS).17-19 ESI has the advantage of being compatible with polar mobile phases, and softMethod for Characterization of Low Molecular Weight Organic Acids in Atmospheric Aerosols Using Ion Chromatography Mass Spectrometry Lacey C. Brent,* Jessica L. Reiner, Russell R. Dickerson, and Lane C. Sander

Dickerson, Russell R.

56

Influence of transport and ocean ice extent on biogenic aerosol sulfur in the Arctic atmosphere  

E-Print Network [OSTI]

Influence of transport and ocean ice extent on biogenic aerosol sulfur in the Arctic atmosphere S, such as methanesulfonic acid (MSA). This study examines relationships between changes in total sea ice extent north of 70. These results suggest that a decrease in seasonal ice cover influencing other mechanisms of DMS production could

57

Mineralogy of Martian atmospheric dust inferred from thermal infrared spectra of aerosols  

E-Print Network [OSTI]

Mineralogy of Martian atmospheric dust inferred from thermal infrared spectra of aerosols Victoria deconvolution algorithm to the spectra to model the dust mineralogy. Models of the M9 IRIS transmission data generally are of poor quality, and the mineralogical results of these fits are unlikely to be valid. Fits

Hamilton, Victoria E.

58

atmospheric aerosol characteristics: Topics by E-print Network  

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

Size Distribution Physics (arXiv) Summary: Atmospheric flows exhibit selfsimilar fractal spacetime fluctuations manifested as the fractal geometry to global cloud cover...

59

atmospheric aerosol processes: Topics by E-print Network  

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

Size Distribution Physics (arXiv) Summary: Atmospheric flows exhibit selfsimilar fractal spacetime fluctuations manifested as the fractal geometry to global cloud cover...

60

atmospheric aerosols apports: Topics by E-print Network  

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

Size Distribution Physics (arXiv) Summary: Atmospheric flows exhibit selfsimilar fractal spacetime fluctuations manifested as the fractal geometry to global cloud cover...

Note: This page contains sample records for the topic "aerosols atmospheric profiling" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


61

atmospheric aerosol samples: Topics by E-print Network  

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

Size Distribution Physics (arXiv) Summary: Atmospheric flows exhibit selfsimilar fractal spacetime fluctuations manifested as the fractal geometry to global cloud cover...

62

atmospheric aerosol particle: Topics by E-print Network  

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

suspension in the fractal fluctuations of vertical wind velocity. The mass or radius (size) distribution for homogeneous suspended atmospheric particulates is expressed as a...

63

atmospheric aerosol particles: Topics by E-print Network  

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

suspension in the fractal fluctuations of vertical wind velocity. The mass or radius (size) distribution for homogeneous suspended atmospheric particulates is expressed as a...

64

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

SciTech Connect (OSTI)

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.

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

2012-06-13T23:59:59.000Z

65

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

E-Print Network [OSTI]

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.

A. M. Selvam

2014-08-14T23:59:59.000Z

66

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

SciTech Connect (OSTI)

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.

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

1983-01-01T23:59:59.000Z

67

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

SciTech Connect (OSTI)

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.

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

1984-05-01T23:59:59.000Z

68

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

SciTech Connect (OSTI)

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)

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)

2013-07-01T23:59:59.000Z

69

Program Abstracts: Formation and Growth of Atmospheric Aerosols  

SciTech Connect (OSTI)

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.

Peter H. McMurry; Markku Kulmala

2006-09-07T23:59:59.000Z

70

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

E-Print Network [OSTI]

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$^...

Piacentini, Rubn D; Micheletti, Mara I; Salum, Graciela M; Maya, Javier; Mancilla, Alexis; Garca, Beatriz

2013-01-01T23:59:59.000Z

71

Atmospheric aerosol microphysics: Formation, characterization, and interaction. Progress report, September 1, 1991--February 28, 1994  

SciTech Connect (OSTI)

This project conducts theoretical and computational studies of the physical transformation processes of aerosols which underlie their atmospheric formation, interaction, transport, and removal and derives results that contribute to improved capabilities for modelling aerosol physical and chemical evolution in support of the environmental component of the National Energy Strategy. The subject of study is submicrometer aerosol particles with primary focus upon the ultrafine fraction. This report summarizes technical progress during the first two and one-half years of the project. Results of calculations of equilibrium vapor pressures over adhering pairs of 50, 100, and 200 nm particles are reported showing substantial depression of equilibrium vapor pressure relative to isolated spheres. Calculations are given of collective, long-range intermolecular energies for irregular particles to be used for growth rate calculations for realistic particles. Molecular dynamic simulations of thermal collisions of small clusters with each other and with single atoms are presented as a function of cluster size in the range from 1 to 8 atoms. Calculations of aerosol condensation in which vapor depletion and heating effects are taken into account for atmospheric cloud nucleation modelling are reported.

Marlow, W.H.

1994-12-31T23:59:59.000Z

72

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

E-Print Network [OSTI]

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 ...

Lee, Shao-Yi

73

Nonequilibrium Atmospheric Secondary Organic Aerosol Formation and Growth.  

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmosphericNuclear Security Administration the Contributions andDataNationalNewportBig Eddy ArcheologicalSolar ThermalNDA(s)

74

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed Newcatalyst phasesData FilesShape, Density,TiO2(110). |Gas-phase Tracer Tests.

75

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

SciTech Connect (OSTI)

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.

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

2014-04-16T23:59:59.000Z

76

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

SciTech Connect (OSTI)

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 Chemistry??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 Earth??s troposphere. Due to the combined computational burden of the coupled system, the currently available computational resources were the limiting factor preventing the adequate statistical analysis of the overall impact that multiphase chemistry might have on climate-scale radiative transfer and climate.

Keene, William C. [University of Virginia] [University of Virginia; Long, Michael S. [University of Virginia] [University of Virginia

2013-05-20T23:59:59.000Z

77

Laboratory Experiments and Instrument Development for the Study of Atmospheric Aerosols  

SciTech Connect (OSTI)

Soot particles are generated by incomplete combustion of fossil and biomass fuels. Through direct effects clear air aerosols containing black carbon (BC) such as soot aerosols, absorb incoming light heating the atmosphere, while most other aerosols scatter light and produce cooling. Even though BC represents only 1-2% of the total annual emissions of particulate mass to the atmosphere, it has been estimated that the direct radiative effect of BC is the second-most important contributor to global warming after absorption by CO2. Ongoing studies continue to underscore the climate forcing importance of black carbon. However, estimates of the radiative effects of black carbon on climate remain highly uncertain due to the complexity of particles containing black carbon. Quantitative measurement of BC is challenging because BC often occurs in highly non-spherical soot particles of complex morphology. Freshly emitted soot particles are typically fractal hydrophobic aggregates. The aggregates consist of black carbon spherules with diameters typically in the range of about 15-40 nm, and they are usually coated by adsorbed polyaromatic hydrocarbons (PAHs) produced during combustion. Diesel-generated soot particles are often emitted with an organic coating composed primarily of lubricating oil and unburned fuel, as well as well as PAH compounds. Sulfuric acid has also been detected in diesel and aircraft-emitted soot particles. In the course of aging, these particle coatings may be substantially altered by chemical reactions and/or the deposition of other materials. Such processes transform the optical and CCN properties of the soot aerosols in ways that are not yet well understood. Our work over the past seven years consisted of laboratory research, instrument development and characterization, and field studies with the central focus of improving our understanding of the black carbon aerosol climate impacts. During the sixth year as well as during this seventh year (no-cost extension period) of our grant, we extended our studies to perform experiments on the controlled production and characterization of secondary organic aerosol.

Davidovits, Paul

2011-12-10T23:59:59.000Z

78

Atmospheric Chemistry, Carbon Cycle, and Climate (AC4): Observational Constraints on Sources and Sinks of Aerosols and Greenhouse Gases  

E-Print Network [OSTI]

and gas extraction can also inform future energy choices. In FY 2014, Atmospheric Chemistry, Carbon Cycle anthropogenic-biogenic emission intense regions 3. Deposition processes controlling atmospheric concentrations of aerosols and greenhouse gases Projects that quantify sources and sinks via new measurements and/or modeling

79

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.

80

Atmospheric pressure flow reactor / aerosol mass spectrometer studies of tropospheric aerosol nucleat and growth kinetics. Final report, June, 2001  

SciTech Connect (OSTI)

The objective of this program was to determine the mechanisms and rates of growth and transformation and growth processes that control secondary aerosol particles in both the clear and polluted troposphere. The experimental plan coupled an aerosol mass spectrometer (AMS) with a chemical ionization mass spectrometer to provide simultaneous measurement of condensed and particle phases. The first task investigated the kinetics of tropospheric particle growth and transformation by measuring vapor accretion to particles (uptake coefficients, including mass accommodation coefficients and heterogeneous reaction rate coefficients). Other work initiated investigation of aerosol nucleation processes by monitoring the appearance of submicron particles with the AMS as a function of precursor gas concentrations. Three projects were investigated during the program: (1) Ozonolysis of oleic acid aerosols as model of chemical reactivity of secondary organic aerosol; (2) Activation of soot particles by measurement deliquescence in the presence of sulfuric acid and water vapor; (3) Controlled nucleation and growth of sulfuric acid aerosols.

Worsnop, Douglas R.

2001-06-01T23:59:59.000Z

Note: This page contains sample records for the topic "aerosols atmospheric profiling" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


81

AAI Absorbing Aerosol Index ADAGUC Atmospheric Data Access for the Geospatial User Community  

E-Print Network [OSTI]

Change IPT Integrated Profiling Technique IR Infrared IsA International standard Atmosphere (recommended by WMO) IsCCP International satellite Cloud Climatology Project IsO International Organization in Europe (EU project) IPC International Pyrheliometer Comparison IPCC Intergovernmental Panel on Climate

Haak, Hein

82

E-Print Network 3.0 - aerosol atmospheric interactions Sample...  

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

for Climate Summary: order estimates of aerosol-climate interaction But... only Earth System Models can include all... of the interactions (in theory at least) 12;Aerosols <>...

83

E-Print Network 3.0 - atmospheric state profiles Sample Search...  

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

Sciences and Ecology 2 INVESTIGATING THERMODYNAMICS OF VERTICAL ATMOSPHERIC ENERGY TRANSPORT Summary: the Earth's radiation entropy fluxes. The vertical profiles of net...

84

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.

85

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

E-Print Network [OSTI]

are conducted under the three aerosol scenarios: 1) the clean case with an aerosol number concentration of 200 cm-1, 2) the polluted case with a number concentration of 1000 cm-1, and 3) the aerosol radiative effects (AR) case with same aerosol concentration...

Lee, Keun-Hee

2012-02-14T23:59:59.000Z

86

A numerical simulation of atmospheric photochemical processes including interactions with aerosol particles  

SciTech Connect (OSTI)

We propose a comprehensive model of atmospheric photochemical processes that can be used to investigate the interactions between gas species and aerosol particles. We considered both gas and particle phase reactions, transport of material between these phases, convection, turbulent diffusion, particle growth, coagulation, nucleation, and sources. The aerosol particle phase is not forced to follow the gas phase in equilibrium; transport to the particles is described by diffusion to the particle surface. The resulting model treats 33 gas phase species and 39 particles phase species; 16 of these are transported between the phases. The particle size distribution is approximated by 9 sections between 0.01 and 10 {mu}m diameter. Strong interactions between the gas and particles are seen. Higher relative humidity results in more particle volume and surface area, allowing the interphase transport to become competitive with the reaction terms. In particular, at high relative humidities the increased scavenging of HO{sub 2} radicals by particles reduces the O{sub 3} maximum concentration. This effect is seen only on days when the maximum relative humidity exceeds 90%. This conclusion has implications for the applicability of models developed for the Los Angeles Basin, where the maximum relative humidity rarely exceeds 75%, to more humid climates like Houston.

Hackler, M.A.

1989-01-01T23:59:59.000Z

87

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.

88

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

SciTech Connect (OSTI)

This report describes the technical progress made on the Pittsburgh Air Quality Study (PAQS) during the period of September 2003 through February 2004. Significant progress was made this project period on the analysis of ambient data, source apportionment, and deterministic modeling activities. Results highlighted in this report include chemical fractionation of the organic fraction to quantify the ratio of organic mass to organic carbon (OM/OC). The average OM/OC ratio for the 31 samples analyzed so far is 1.89, ranging between 1.62 and 2.53, which is consistent with expectations for an atmospherically processed regional aerosol. Analysis of the single particle data reveals that a on a particles in Pittsburgh consist of complex mixture of primary and secondary components. Approximately 79% of all particles measured with the instrument containing some form of carbon, with Carbonaceous Ammonium Nitrate (54.43%) being the dominant particle class. PMCAMx predictions were compared with data from more than 50 sites of the STN network located throughout the Eastern United States for the July 2001 period. OC and sulfate concentrations predicted by PMCAMx are within {+-}30% of the observed concentration at most of these sites. Spherical Aluminum Silicate particle concentrations (SAS) were used to estimate the contribution of primary coal emissions to fine particle levels at the central monitoring site. Primary emissions from coal combustion contribute on average 0.44 {+-} 0.3 {micro}g/m{sup 3} to PM{sub 2.5} at the site or 1.4 {+-} 1.3% of the total PM{sub 2.5} mass. Chemical mass balance analysis was performed to apportion the primary organic aerosol. About 70% of the primary OC emissions are from vehicular sources, with the gasoline contribution being on average three times greater than the diesel emissions in the summer.

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

2004-04-01T23:59:59.000Z

89

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

E-Print Network [OSTI]

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 ...

Blackwell, William Joseph, 1971-

2002-01-01T23:59:59.000Z

90

Atmospheric Aerosol Source-Receptor Relationships: The Role of Coal-Fired Power Plants  

SciTech Connect (OSTI)

This report describes the technical progress made on the Pittsburgh Air Quality Study (PAQS) during the period of March 2005 through August 2005. Significant progress was made this project period on the source characterization, source apportionment, and deterministic modeling activities. This report highlights new data on road dust, vegetative detritus and motor vehicle emissions. For example, the results show significant differences in the composition in urban and rural road dust. A comparison of the organic of the fine particulate matter in the tunnel with the ambient provides clear evidence of the significant contribution of vehicle emissions to ambient PM. The source profiles developed from this work are being used by the source-receptor modeling activities. The report presents results on the spatial distribution of PMF-factors. The results can be grouped into three different categories: regional sources, local sources, or potentially both regional and local sources. Examples of the regional sources are the sulfate and selenium PMF-factors which most likely-represent coal fired power plants. Examples of local sources are the specialty steel and lead factors. There is reasonable correspondence between these apportionments and data from the EPA TRI and AIRS emission inventories. Detailed comparisons between PMCAMx predictions and measurements by the STN and IMPROVE measurements in the Eastern US are presented. Comparisons were made for the major aerosol components and PM{sub 2.5} mass in July 2001, October 2001, January 2002, and April 2002. The results are encouraging with average fraction biases for most species less than 0.25. The improvement of the model performance during the last two years was mainly due to the comparison of the model predictions with the continuous measurements in the Pittsburgh Supersite. Major improvements have included the descriptions: of ammonia emissions (CMU inventory), night time nitrate chemistry, EC emissions and their diurnal variation, and nitric acid dry removal.

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

2005-12-01T23:59:59.000Z

91

Development of an atmospheric aerosol model for studies of global budgets and effects of airborne particulate material  

SciTech Connect (OSTI)

A microphysics-removal Atmospheric Aerosol Model (AAM) is developed for use in General Circulation Models (GCM) to study global budgets and effects of particulate material. In this model the particle population is assumed to be composed of a set of log-normal modes whose time evolution due to microphysical processes is described via prognostic equations for an appropriate number of moments of the particle size distribution. This newly devised technique, by making use of a small number of prognostic equations for the aerosol variables and utilizing optimized numerical procedures, renders the model computationally efficient, hence particularly suitable for use in complex 3D GCMs. Detailed parameterizations of particle coagulation, sedimentation, dry deposition, and wet removal are incorporated into the AAM.

Giorgi, F.

1986-01-01T23:59:59.000Z

92

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

E-Print Network [OSTI]

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...

Fornea, Adam P.

2010-07-14T23:59:59.000Z

93

E-Print Network 3.0 - atmospheric aerosol concentration Sample...  

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

and absorb shortwave (solar) radiation and... of the U.S. Department of Energy under Contract No. DE-AC02-98CH10886. AEROSOLS AND CLIMATE CHANGE... : A TUTORIAL S. E. Schwartz...

94

E-Print Network 3.0 - atmospheric aerosol desarrollo Sample Search...  

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

and absorb shortwave (solar) radiation and... of the U.S. Department of Energy under Contract No. DE-AC02-98CH10886. AEROSOLS AND CLIMATE CHANGE... : A TUTORIAL S. E. Schwartz...

95

E-Print Network 3.0 - affect atmospheric aerosols Sample Search...  

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

and absorb shortwave (solar) radiation and... of the U.S. Department of Energy under Contract No. DE-AC02-98CH10886. AEROSOLS AND CLIMATE CHANGE... : A TUTORIAL S. E. Schwartz...

96

The Evolution of the Physicochemical Properties of Aerosols in the Atmosphere  

E-Print Network [OSTI]

A Differential Mobility Analyzer/Tandem Differential Mobility Analyzer (DMA/TDMA) system was used to measure simultaneously the size distribution and hygroscopicity of the ambient aerosol population. The system was operated aboard the National...

Tomlinson, Jason

2011-02-22T23:59:59.000Z

97

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmosphericNuclear Security Administration the Contributions andDataNational Library of1, 2007TransmissiontoSystemNewApproaches3 New

98

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

SciTech Connect (OSTI)

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.

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

2014-09-01T23:59:59.000Z

99

Origin of atmospheric aerosols at the Pierre Auger Observatory using studies of air mass trajectories in South America  

E-Print Network [OSTI]

The Pierre Auger Observatory is making significant contributions towards understanding the nature and origin of ultra-high energy cosmic rays. One of its main challenges is the monitoring of the atmosphere, both in terms of its state variables and its optical properties. The aim of this work is to analyze aerosol optical depth $\\tau_{\\rm a}(z)$ values measured from 2004 to 2012 at the observatory, which is located in a remote and relatively unstudied area of the Pampa Amarilla, Argentina. The aerosol optical depth is in average quite low - annual mean $\\tau_{\\rm a}(3.5~{\\rm km})\\sim 0.04$ - and shows a seasonal trend with a winter minimum - $\\tau_{\\rm a}(3.5~{\\rm km})\\sim 0.03$ -, and a summer maximum - $\\tau_{\\rm a}(3.5~{\\rm km})\\sim 0.06$ -, and an unexpected increase from August to September - $\\tau_{\\rm a}(3.5~{\\rm km})\\sim 0.055$). We computed backward trajectories for the years 2005 to 2012 to interpret the air mass origin. Winter nights with low aerosol concentrations show air masses originating from t...

Curci, Gabriele

2014-01-01T23:59:59.000Z

100

Atmospheric multiple scattering of fluorescence light from extensive air showers and effect of the aerosol size on the reconstruction of energy and depth of maximum  

E-Print Network [OSTI]

The reconstruction of the energy and the depth of maximum $X_{\\rm max}$ of an extensive air shower depends on the multiple scattering of fluorescence photons in the atmosphere. In this work, we explain how atmospheric aerosols, and especially their size, scatter the fluorescence photons during their propagation. Using a Monte Carlo simulation for the scattering of light, the dependence on the aerosol conditions of the multiple scattered light contribution to the recorded signal is fully parameterised. A clear dependence on the aerosol size is proposed for the first time. Finally, using this new parameterisation, the effect of atmospheric aerosols on the energy and on the $X_{\\rm max}$ reconstructions is presented for a vertical extensive air shower observed by a ground-based detector at $30~$km: for typical aerosol conditions, multiple scattering leads to a systematic over-estimation of $5\\pm1.5\\%$ for the energy and $4.0\\pm 1.5~$g/cm$^2$ for the $X_{\\rm max}$, where the uncertainties refer to a variation of the aerosol size.

K. Louedec; J. Colombi

2014-03-17T23:59:59.000Z

Note: This page contains sample records for the topic "aerosols atmospheric profiling" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


101

Continuous Profiles of Cloud Microphysical Properties for the Fixed Atmospheric Radiation Measurement Sites  

SciTech Connect (OSTI)

The Atmospheric Radiation Measurement (ARM) Program defined a specific metric for the third quarter of Fiscal Year 2006 to produce and refine a one-year continuous time series of cloud microphysical properties based on cloud radar measurements for each of the fixed ARM sites. To accomplish this metric, we used a combination of recently developed algorithms that interpret radar reflectivity profiles, lidar backscatter profiles, and microwave brightness temperatures into the context of the underlying cloud microphysical structure.

Jensen, M; Jensen, K

2006-06-01T23:59:59.000Z

102

Effects of aerosol species on atmospheric visibility in Kaohsiung City, Taiwan  

SciTech Connect (OSTI)

Visibility data collected from Kaohsiung City, Taiwan, for the past two decades indicated that the air pollutants have significantly degraded visibility in recent years. During the study period, the seasonal mean visibilities in spring, summer, fall, and winter were only 5.4, 9.1, 8.2, and 3.4 km, respectively. To ascertain how urban aerosols influence the visibility, we conducted concurrent visibility monitoring and aerosol sampling in 1999 to identify the principal causes of visibility impairments in the region. In this study, ambient aerosols were sampled and analyzed for 11 constituents, including water-soluble ions and carbon materials, to investigate the chemical composition of Kaohsiung aerosols. Stepwise regression method was used to correlate the impact of aerosol species on visibility impairments. Both seasonal and diurnal variation patterns were found from the monitoring of visibility. Results showed that light scattering was attributed primarily to aerosols with sizes that range from 0.26 to 0.90 {mu}m, corresponding with the wavelength region of visible light, which accounted for {approximately} 72% of the light scattering coefficient. Sulfate was a dominant component that affected both the light scattering coefficient and the visibility in the region. On average, (NH{sub 4}){sup 2}SO{sub 4}, NH{sub 4}NO{sub 3}, total carbon, and fine particulate matter (PM2.5)-remainder contributed 53%, 17%, 16%, and 14% to total light scattering, respectively. An empirical regression model of visibility based on sulfate, elemental carbon, and humidity was developed, and the comparison indicated that visibility in an urban area could be properly simulated by the equation derived herein. 35 refs., 10 figs., 4 tabs.

Chang-Gai Lee; Chung-Shin Yuan; Jui-Cheng Chang; Ching Yuan [National Sun Yat-Sen University (Taiwan)

2005-07-01T23:59:59.000Z

103

Atmospheric Aerosols Aging Involving Organic Compounds and Impacts on Particle Properties  

E-Print Network [OSTI]

through sandstorm.2 Examples of anthropogenic sources are vehicle exhaust, plant emission, and construction sites. Some aerosols may have both biogenic and anthropogenic sources. For example, soot aerosols, also known as black carbon, can be produced... with an initial size of 150 nm increases slightly faster than those of soot with the initial size of 80 or 100 nm. Table 1. Properties of Fresh Soot Particles. Dp, nm mp, 10 ?16 g Dve, nm Npp a 82.4 1.47 54.1 20 101 2.34 63.2 32 155 7.77 94.3 105 a...

Qiu, Chong

2013-02-01T23:59:59.000Z

104

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

SciTech Connect (OSTI)

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.

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

2011-07-06T23:59:59.000Z

105

Comparison of temperature and humidity profiles with elastic-backscatter lidar data  

SciTech Connect (OSTI)

This contribution analyzes elastic-backscatter lidar data and temperature and humidity profiles from radiosondes acquired in Barcelona in July 1992. Elastic-backscatter lidar data reveal the distribution of aerosols within the volume of atmosphere scanned. By comparing this information with temperature and humidity profiles of the atmosphere at a similar time, we are able to asses de relationship among aerosol distribution and atmospheric stability or water content, respectively. Comparisons have shown how lidar`s revealed layers of aerosols correspond to atmospheric layers with different stability condition and water content.

Soriano, C. [Universidad Politecnica de Cataluna, Barcelona (Spain)]|[Los Alamos National Lab., NM (United States); Buttler, W.T. [Los Alamos National Lab., NM (United States); Baldasano, J.M. [Universidad Politecnica de Cataluna, Barcelona (Spain)

1995-04-01T23:59:59.000Z

106

Final Report "Nucleation and Growth of Atmospheric Aerosols" DOE Grant No. DE-FG02-98ER62556  

SciTech Connect (OSTI)

Research that was supported by this contract has contributed substantially to progress in our understanding of new particle formation in the atmosphere. Objectives included the development of new measurement methods, the application of those new instrument systems in atmospheric field studies, and the interpretation of results from those studies. We developed the "Nano TDMA" to measure the hygroscopicity and volatility of 4-20 nm particles. We used this instrument system to characterize properties of atmospheric particles in the Atlanta atmosphere in July/August 2002 as well as to study properties of diesel exhaust particles. We also developed the thermal desorption chemical ionization mass spectrometer (TDCIMS) to measure the chemical composition of nanoparticles as small as 7 nm with a time resolution of 10-20 minutes. The TDCIMS is currently the only instrument that can perform such measurements. Atmospheric field measurements were carried out in Atlanta (July/August 2002; we refer to this as the ANARChE study) and in Boulder, CO (2003/04). In the ANARChE study we measured, for the first time, the composition of freshly nucleated particles as small as 7 nm using the TDCIMS. The ANARChE study also included the first nano-TDMA measurements of the volatility and hygroscopicity of freshly nucleated particles as small as 4 nm. Other parameters that were measured included particle size distributions (3 nm-2 m), and sulfuric acid and ammonia concentrations. Key discoveries from the ANARChE study are: (1) freshly nucleated particles in Atlanta consist primarily of ammonium and sulfate; evidence for significant amounts of other species such as organics and nitrates was not found; (2) new particle formation occurs when rates of cluster loss to preexisting particles are small compared to rates of lost to the next larger cluster size by growth; a dimensionless parameter L describes the ratio of these rates, and measurements showed that new particle formation was always observed when L was less than one and not when L was greater than one; (3) growth rates of freshly nucleated particles could be explained by condensation of sulfuric acid and coagulation of the newly formed nucleation mode in the mornings when particles were small (<20 nm), but at midday when particles had growth to larger sizes measured growth rates were often five times greater than calculated growth rates suggesting that species in addition to sulfuric acid were contributing to growth. This contract also supported TDCIMS and aerosol physical property measurements performed at NCAR?s Mesa Laboratory in Boulder, CO, intermittently since the Spring of 2002. The TDCIMS measurements were made on sub-20 nm diameter atmospheric particles, and have uncovered many intriguing questions that warrant further investigation. For example, unlike the case in Atlanta where primarily ammonium was observed in the positive ion spectrum for ambient aerosol, Boulder aerosols appear to be composed of a variety of compounds most of which have not been identified. In the negative ion spectrum, Boulder sub-20 nm diameter particles are characterized by large nitrate peaks, with integrated areas up to 3 orders of magnitude greater than aerosol sulfate.

Peter H. McMurry; James N. Smith; Fred L. Eisele

2005-06-02T23:59:59.000Z

107

JOURNAL OF GEOPHYSICAL RESEARCH, VOL. 102, NO. D24, PAGES 29,737-29,745, DECEMBER 26, 1997 Atmospheric aerosol and water vapor characteristics over north  

E-Print Network [OSTI]

Atmospheric aerosol and water vapor characteristics over north central Canada during BOREAS B. L. Markham, J typically0.09 and 0.34 cm, respectively.Size distributionsderivedfrom solar almucantarmeasurementsshowtheHughesSTXCorporation,Greenbelt,Maryland. 2Formerlyat HSTX/GSFC-NASA,Greenbelt,Maryland. Copyright1997by the American

108

E-Print Network 3.0 - atmospheric aerosol emissions Sample Search...  

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

Top-level Science Question: What are the effects of gaseous and particulate emissions and climate variability and change on global atmospheric composition, Summary: of the...

109

Development of an atmospheric aerosol model for studies of global budgets and effects of airborne particulate material  

SciTech Connect (OSTI)

A microphysics-removal atmospheric aerosol model (AAM) is developed for use in general circulation models (GCMs) to study global budgets and effects of particulate material. In this model the particle population is composed of a set of log-normal modes whose time evolution due to microphysical processes is described via prognostic equations for an appropriate number of moments of the particle-size distribution. Detailed parameterizations of particle coagulation, sedimentation, dry deposition, and wet removal are developed and implemented into the AAM. The AAM is incorporated into a GCM and is applied to two types of studies: (1) characteristics of the particle wet and dry removal processes, and (2) climatic impact of massive particulate injections following a global nuclear war, with emphasis on the sensitivity of the simulated effects to the inclusion of particle microphysics. Results are discussed.

Giorgi, F.

1986-01-01T23:59:59.000Z

110

Evaluation of Hydrometeor Occurrence Profiles in the Multiscale Modeling Framework Climate Model using Atmospheric Classification  

SciTech Connect (OSTI)

Vertical profiles of hydrometeor occurrence from the Multiscale Modeling Framework (MMF) climate model are compared with profiles observed by a vertically pointing millimeter wavelength cloud-radar (located in the U.S. Southern Great Plains) as a function of the largescale atmospheric state. The atmospheric state is determined by classifying (or clustering) the large-scale (synoptic) fields produced by the MMF and a numerical weather prediction model using a neural network approach. The comparison shows that for cold frontal and post-cold frontal conditions the MMF produces profiles of hydrometeor occurrence that compare favorably with radar observations, while for warm frontal conditions the model tends to produce hydrometeor fractions that are too large with too much cloud (non-precipitating hydrometeors) above 7 km and too much precipitating hydrometeor coverage below 7 km. We also find that the MMF has difficulty capturing the formation of low clouds and that for all atmospheric states that occur during June, July, and August, the MMF produces too much high and thin cloud, especially above 10 km.

Marchand, Roger T.; Beagley, Nathaniel; Ackerman, Thomas P.

2009-09-01T23:59:59.000Z

111

SUPPLEMENTARY MATERIALS Exploring the vertical profile of atmospheric organic aerosol: comparing 17 aircraft field campaigns  

E-Print Network [OSTI]

values. #12;Figure S2: Scatter plot of observed acetonitrile and OA concentrations for seven campaigns in black. 80th percentile acetonitrile concentrations for each campaign are indicated with a dashed line

Meskhidze, Nicholas

112

Experimental and theoretical investigation of nucleation and growth of atmospheric aerosols  

E-Print Network [OSTI]

, and a theoretical study of atmospheric molecular complexes and clusters. The nucleation rate was considerably enhanced in the presence of cis-pinonic acid and ammonia. The composition of the critical cluster was estimated from the dependence...

Zhao, Jun

2009-05-15T23:59:59.000Z

113

WHAT DO SPECTRAL LINE PROFILE ASYMMETRIES TELL US ABOUT THE SOLAR ATMOSPHERE?  

SciTech Connect (OSTI)

Recently, analysis of solar spectra obtained with the EUV Imaging Spectrograph (EIS) onboard the Hinode satellite has revealed the ubiquitous presence of asymmetries in transition region (TR) and coronal spectral line profiles. These asymmetries have been observed especially at the footpoints of coronal loops and have been associated with strong upflows that may play a significant role in providing the corona with hot plasma. Here, we perform a detailed study of the various processes that can lead to spectral line asymmetries, using both simple forward models and state-of-the-art three-dimensional radiative MHD simulations of the solar atmosphere using the Bifrost code. We describe a novel technique to determine the presence and properties of faint secondary components in the wings of spectral line profiles. This method is based on least-squares fitting of observed so-called R(ed)B(lue) asymmetry profiles with pre-calculated RB asymmetry profiles for a wide variety of secondary component properties. We illustrate how this method could be used to perform reliable double Gaussian fits that are not over- or under-constrained. We also find that spectral line asymmetries appear in TR and coronal lines that are synthesized from our three-dimensional MHD simulations. Our models show that the spectral asymmetries are a sensitive measure of the velocity gradient with height in the TR of coronal loops. The modeled TR shows a large gradient of velocity that increases with height: this occurs as a consequence of ubiquitous, episodic heating at low heights in the model atmosphere. We show that the contribution function of spectral lines as a function of temperature is critical for sensitivity to velocity gradients and thus line asymmetries: lines that are formed over a temperature range that includes most of the TR are the most sensitive. As a result, lines from lithium-like ions (e.g., O VI) are found to be the most sensitive to line asymmetries. We compare the simulated line profiles directly with line profiles observed in the quiet Sun with SOHO/SUMER and Hinode/EIS and find that the shape of the profiles is very similar. In addition, the simulated profiles with the strongest blueward asymmetry occur in footpoint regions of coronal loops, which is similar to what we observe with SUMER and EIS. There is however a significant discrepancy between the simulations and observations: the simulated RB asymmetries are an order of magnitude smaller than the observations. We discuss the possible reasons for this discrepancy. In summary, our analysis shows that observations of spectral line asymmetries can provide a powerful new diagnostic to help constrain coronal heating models.

MartInez-Sykora, Juan; De Pontieu, Bart [Lockheed Martin Solar and Astrophysics Laboratory, Palo Alto, CA 94304 (United States); Hansteen, Viggo [Institute of Theoretical Astrophysics, University of Oslo, P.O. Box 1029 Blindern, N-0315 Oslo (Norway); McIntosh, Scott W., E-mail: j.m.sykora@astro.uio.no [High Altitude Observatory, National Center for Atmospheric Research, Boulder, CO 80307 (United States)

2011-05-10T23:59:59.000Z

114

2.1 RAMAN LIDAR PROFILING OF WATER VAPOR AND AEROSOLS OVER THE ARM SGP SITE  

E-Print Network [OSTI]

with satellite sensors. Accurate, high spatial and temporal resolution profiles of water vapor are also required+GOES) have been combined into a single product that takes advantage of both active and passive remote sensors with the use of narrowband (~0.4 nm bandpass) filters, reduces the background skylight and, therefore

115

The importance of aerosol mixing state and size-resolved composition on CCN concentration and the variation of the importance with atmospheric aging of aerosols  

SciTech Connect (OSTI)

Aerosol microphysics, chemical composition, and CCN concentrations were measured at the T0 urban supersite in Mexico City during Megacity Initiative: Local and Global Research Observations (MILAGRO) in March 2006. The aerosol size distribution and composition often showed strong diurnal variation associated with traffic emissions and aging of aerosols through coagulation and local photochemical production of secondary aerosol species. CCN concentrations (N{sub CCN}) are derived using Kohler theory from the measured aerosol size distribution and various simplified aerosol mixing state and chemical composition, and are compared to concurrent measurements at five supersaturations ranging from 0.11% to 0.35%. The influence of assumed mixing state on calculated N{sub CCN} is examined using both aerosols observed during MILAGRO and representative aerosol types. The results indicate that while ambient aerosols often consist of particles with a wide range of compositions at a given size, N{sub CCN} may be derived within {approx}20% assuming an internal mixture (i.e., particles at a given size are mixtures of all participating species, and have the identical composition) if great majority of particles has an overall {kappa} (hygroscopicity parameter) value greater than 0.1. For a non-hygroscopic particle with a diameter of 100 nm, a 3 nm coating of sulfate or nitrate is sufficient to increase its {kappa} from 0 to 0.1. The measurements during MILAGRO suggest that the mixing of non-hygroscopic primary organic aerosol (POA) and black carbon (BC) particles with photochemically produced hygroscopic species and thereby the increase of their {kappa} to 0.1 take place in a few hours during daytime. This rapid process suggests that during daytime, a few tens of kilometers away for POA and BC sources, N{sub CCN} may be derived with sufficient accuracy by assuming an internal mixture, and using bulk chemical composition. The rapid mixing also indicates that, at least for very active photochemical environments such as Mexico City, a substantially shorter timescale during daytime for the conversion of hydrophobic POA and BC to hydrophilic particles than the 1-2 days used in some global models. The conversion time scale is substantially longer during night. Most POA and BC particles emitted during evening hours likely remain non-hygroscopic until efficiently internally mixed with secondary species in the next morning. The results also suggest that the assumed mixing state strongly impacts calculated N{sub CCN} only when POA and BC represent a large fraction of the total aerosol volume. One of the implications is that while physically unrealistic, external mixtures, which are used in many global models, may also sufficiently predict N{sub CCN} for aged aerosol, as the contribution of non-hygroscopic POA and BC to overall aerosol volume is often substantially reduced due to the condensation of secondary species.

Wang, J.; Cubison, M. J.; Aiken, A. C.; Jimenez, J. L.; Collins, D. R.

2010-05-01T23:59:59.000Z

116

Development and Characterization of a Thermodenuder for Aerosol Volatility Measurements  

SciTech Connect (OSTI)

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.

Dr. Timothy Onasch

2009-09-09T23:59:59.000Z

117

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmosphericNuclear Security Administration the1 - September 2006PhotovoltaicSeptember 22, 2014SocietyJ. Dudhia51 Posters7551

118

Comparative Analysis of Urban Atmospheric Aerosol by Particle-Induced X-ray  

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed New SubstationCleanCommunity Involvement and Making aCompactCompany TemplateEmission

119

About EffectiveŽ 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth (AOD)ProductssondeadjustsondeadjustAbout the Building Technologies Office About theofAbout SHARE About

120

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

SciTech Connect (OSTI)

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.

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

2005-04-01T23:59:59.000Z

Note: This page contains sample records for the topic "aerosols atmospheric profiling" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


121

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

SciTech Connect (OSTI)

This report describes the technical progress made on the Pittsburgh Air Quality Study (PAQS) during the period of March 2004 through August 2004. Significant progress was made this project period on the analysis of ambient data, source apportionment, and deterministic modeling activities. Results highlighted in this report include evaluation of the performance of PMCAMx+ for an air pollution episode in the Eastern US, an emission profile for a coke production facility, ultrafine particle composition during a nucleation event, and a new hybrid approach for source apportionment. An agreement was reached with a utility to characterize fine particle and mercury emissions from a commercial coal fired power. Research in the next project period will include source testing of a coal fired power plant, source apportionment analysis, emission scenario modeling with PMCAMx+, and writing up results for submission as journal articles.

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

2004-12-01T23:59:59.000Z

122

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

SciTech Connect (OSTI)

This report describes the technical progress made on the Pittsburgh Air Quality Study (PAQS) during the period of March 2003 through August 2003. Significant progress was made this project period on the source characterization, source apportionment, and deterministic modeling activities. Major accomplishments included: Development of an emission profile for an integrated coke production facility and simulations using PMCAMx for a two week period during July 2001. The emissions from the coke facility are dominated by carbonaceous compounds. Forty seven percent of the organic carbon mass was identified on a compound level basis. Polycyclic aromatic hydrocarbons were the dominant organic compound class in the coke emissions. Initial comparisons with the data collected in Pittsburgh suggest good agreement between the model predictions and observations. Single particle composition data appear useful for identifying primary sources. An example of this unique approach is illustrated using the Fe and Ce particle class with appear associated with steel production.

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

2003-11-01T23:59:59.000Z

123

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)

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.

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

2013-11-08T23:59:59.000Z

124

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

E-Print Network [OSTI]

possible pollutant sources. Keywords Atmospheric aerosols . Canonical correlation analysis . Chicago air pollution studies involve collection and anal- ysis of atmospheric aerosols and concurrent meteorol- ogy) and principal component analysis (PCA) were applied to atmospheric aerosol and trace gas concentrations

O'Brien, Timothy E.

125

Atmospheric Radiation Measurement (ARM) Data from Cape Cod, Massachusetts for the Two-Column Aerosol Project (TCAP)  

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

The Two-Column Aerosol Project (TCAP) was designed to 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 ARM Mobile Facility and the Mobile Aerosol Observing System were deployed 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 were supplemented by two aircraft intensive observation periods, one in the summer and a second in the winter.

126

EMSL - Atmospheric Aerosol Systems  

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May JunDatastreamsmmcrcalgovInstrumentsruc DocumentationP-Series to UserProduct:DirectivesSAND2015-21271 7 6 EIA-176Page 1What's New

127

Atmospheric Aerosols Workshop | EMSL  

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May JunDatastreamsmmcrcalgovInstrumentsruc DocumentationP-Series to someone byDear Friend,Arthur J. Nozik -GrownAn overhead

128

aerosol ratio program: Topics by E-print Network  

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

contribute a major portion of atmospheric aerosol mass loading 5. The estimated global annual Liou, K. N. 2 Studying Clouds and Aerosols with Lidar Depolarization Ratio and...

129

aerosol optical thickness: Topics by E-print Network  

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

of solar radiation by atmospheric aerosols is a key el- ement of the Earth's radiative energy balance and climate. The optical properties of aerosol particles are, however,...

130

aerosol black carbon: Topics by E-print Network  

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

of solar radiation by atmospheric aerosols is a key el- ement of the Earth's radiative energy balance and climate. The optical properties of aerosol particles are, however,...

131

The Indirect and Semi-Direct Aerosol Campaign  

ScienceCinema (OSTI)

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

Ghan, Steve

2014-06-12T23:59:59.000Z

132

The Indirect and Semi-Direct Aerosol Campaign  

SciTech Connect (OSTI)

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

Ghan, Steve

2014-03-24T23:59:59.000Z

133

aerosol research study: Topics by E-print Network  

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

in atmospheric thermal structure, burning, bio-sources changes? 12;Aerosol microphysics: size distribution, mixing state, morphology, shape 9 Aerosol Science and Technology,...

134

Atmospheric aerosol light scattering and surface wetness influence the diurnal pattern of net ecosystem exchange in a semi-arid  

E-Print Network [OSTI]

and can enhance terrestrial carbon sequestration (Gu et al., 1999, 2002, 2003; Roderick et al., 2001 observational evidence of a link between routine aerosol variability, diffuse radiation and carbon sequestration.g. Baldocchi, 1997). Relation- ships using these variables have been used to model carbon exchange between

Cohen, Ronald C.

135

Remote sensing of terrestrial tropospheric aerosols from aircraft and satellites  

E-Print Network [OSTI]

Remote sensing of terrestrial tropospheric aerosols from aircraft and satellites M I Mishchenko1 instruments suitable for aerosol remote sensing and give examples of aerosol retrievals obtained forcing directly by absorbing and reflecting sunlight, thereby cooling or heating the atmosphere

136

Aerosol remote sensing in polar regions  

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

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 ngstrm'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 winterspring and summerautumn 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 winterspring, 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-lesund. 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 surfaceatmosphere system over polar regions.

Tomasi, C.; Wagener, R.; Kokhanovsky, A. A.; Lupi, A.; Ritter, C.; Smirnov, A.; O Neill, N. T.; Stone, R. S.; Holben, B. N.; Nyeki, S.; Wehrli, C.; Stohl, A.; Mazzola, M.; Lanconelli, C.; Vitale, V.; Stebel, K.; Aaltonen, V.; de Leeuw, G.; Rodriguez, E.; Herber, A. B.; Radionov, V. F.; Zielinski, T.; Petelski, T.; Sakerin, S. M.; Kabanov, D. M.; Xue, Y.; Mei, L.; Istomina, L.; Wagener, R.; McArthur, B.; Sobolewski, P. S.; Kivi, R.; Courcoux, Y.; Larouche, P.; Broccardo, S.; Piketh, S. J.

2015-01-01T23:59:59.000Z

137

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

SciTech Connect (OSTI)

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.

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

1999-07-01T23:59:59.000Z

138

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]

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 ...

Hohaus, T.

139

aerosols | EMSL  

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

aerosols aerosols Leads No leads are available at this time. Magnesium behavior and structural defects in Mg+ ion implanted silicon carbide. Abstract: As a candidate material for...

140

Direct Aerosol Forcing Uncertainty  

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

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.

Mccomiskey, Allison

Note: This page contains sample records for the topic "aerosols atmospheric profiling" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


141

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

SciTech Connect (OSTI)

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

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

2013-06-05T23:59:59.000Z

142

E-Print Network 3.0 - aerosolized polymerized type Sample Search...  

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

spheric aerosol particles and isolated from fog... in atmospheric aerosol particles and rainwater in the 1980's (Si- moneit, 1980; Likens and ... Source: Ecole Polytechnique,...

143

Large Aerosols Play Unexpected Role in Ganges Valley | U.S. DOE...  

Office of Science (SC) Website

The data have revealed that large aerosols in this region absorb a greater amount of light than expected. The Science Aerosol particles in the atmosphere may absorb solar...

144

Chemical Bonding and Structural Information of Black CarbonReference Materials and Individual Carbonaceous AtmosphericAerosols  

SciTech Connect (OSTI)

The carbon-to-oxygen ratios and graphitic nature of a rangeof black carbon standard reference materials (BC SRMs), high molecularmass humic-like substances (HULIS) and atmospheric particles are examinedusing scanning transmission X-ray microscopy (STXM) coupled with nearedge X-ray absorption fine structure (NEXAFS) spectroscopy. UsingSTXM/NEXAFS, individual particles with diameter>100 nm are studied,thus the diversity of atmospheric particles collected during a variety offield missions is assessed. Applying a semi-quantitative peak fittingmethod to the NEXAFS spectra enables a comparison of BC SRMs and HULIS toparticles originating from anthropogenic combustion and biomass burns,thus allowing determination of the suitability of these materials forrepresenting atmospheric particles. Anthropogenic combustion and biomassburn particles can be distinguished from one another using both chemicalbonding and structural ordering information. While anthropogeniccombustion particles are characterized by a high proportion ofaromatic-C, the presence of benzoquinone and are highly structurallyordered, biomass burn particles exhibit lower structural ordering, asmaller proportion of aromatic-C and contain a much higher proportion ofoxygenated functional groups.

Hopkins, Rebecca J.; Tivanski, Alexei V.; Marten, Bryan D.; Gilles, Mary K.

2007-04-25T23:59:59.000Z

145

Headspace profiles of modified atmosphere packaged fresh red snapper (Lutjanus campechanus) by gas liquid chromatography  

E-Print Network [OSTI]

activity. Typical components found in the headspace were, butanal, ethanol, hexanal, dimethylamine and trimethylamine. During storage at 4 C, the microbial population within the packages containing C02 tended to shift from an initial gram negative... dioxide (CO2) enriched atmospheres and vacuum packaging have become important new technologies that will improve the quality and shelf-life of fresh seafood products. This type of packaging not only extends the shelf-life of seafoods, it also makes...

Scorah, Craig Darrell Allen

1988-01-01T23:59:59.000Z

146

Atomic Force and Scanning Electron Microscopy of Atmospheric Particles  

E-Print Network [OSTI]

conducted so as to characterize atmospheric aerosols from anthropogenic (pollution) and natural (sea saltAtomic Force and Scanning Electron Microscopy of Atmospheric Particles ZAHAVA BARKAY,1 * AMIT 69978, Israel KEY WORDS atmospheric aerosols; atomic force microscopy; scanning electron microscopy

Shapira, Yoram

147

Integrated Study of MFRSR-derived Parameters of Atmospheric Aerosols and Trace Gases Over the ARM CART Site Extended Facili...  

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation ProposedUsingFunInfrared Land SurfaceVirus-Infected Macaques throughBiomass

148

8, 68456901, 2008 Aerosol optical  

E-Print Network [OSTI]

of solar radiation by atmospheric aerosols is a key el- ement of the Earth's radiative energy balance, Germany 2 Helmholtz Center Munich, German Research Center for Environmental Health, Institute

Paris-Sud XI, Université de

149

Stratospheric and mesospheric pressure-temperature profiles from rotational analysis of CO2 lines in atmospheric trace molecule spectroscopy/ATLAS 1 infrared solar occultation spectra  

SciTech Connect (OSTI)

A simple, classical, and expedient method for the retrieval of atmospheric pressure-temperature profiles has been applied to the high-resolution infrared solar absorption spectra obtained with the atmospheric trace molecule spectroscopy (ATMOS) instrument. The basis for this method is a rotational analysis of retrieved apparent abundances from CO2 rovibrational absorption lines, employing existing constituent concentration retrieval software used in the analysis of data returned by ATMOS. Pressure-temperature profiles derived from spectra acquired during the ATLAS 1 space shuttle mission of March-April 1992 are quantitatively evaluated and compared with climatological and meteorological data as a means of assessing the validity of this approach.

Stiller, G.P.; Gunson, M.R.; Lowes, L.L.; Abrams, M.C.; Raper, O.F.; Farmer, C.B.; Zander, R.; Rinsland, C.P. [Kernforschungszentrum Karlsruhe, Karlsruhe (Germany)] [Kernforschungszentrum Karlsruhe, Karlsruhe (Germany); [Jet Propulsion Lab., California Inst. of Tech., Pasadena, CA (United States); [Liege Univ., Liege (Belgium); [NASA, Langley Research Center, Hampton, VA (United States)

1995-02-01T23:59:59.000Z

150

Constraining the influence of natural variability to improve estimates of global aerosol indirect effects in a nudged version of the Community Atmosphere Model 5  

E-Print Network [OSTI]

Zhao (2006), A simulated climatology of Asian dust aerosolN) PI (F) ? PI (F) ? X ? 2000 (PD Climatology) ? ? 2000 (PD Climatology) ? PD (F) X a All simulations used the same

Kooperman, Gabriel J; Pritchard, Michael S; Ghan, Steven J; Wang, Minghuai; Somerville, Richard C. J; Russell, Lynn M

2012-01-01T23:59:59.000Z

151

Highly stable aerosol generator  

DOE Patents [OSTI]

An improved compressed air nebulizer has been developed such that a uniform aerosol particle size and concentration may be produced over long time periods. This result is achieved by applying a vacuum pressure to the makeup assembly and by use of a vent tube between the atmosphere and the makeup solution. By applying appropriate vacuum pressures to the makeup solution container and by proper positioning of the vent tube, a constant level of aspirating solution may be maintained within the aspirating assembly with aspirating solution continuously replaced from the makeup solution supply. This device may also be adapted to have a plurality of aerosol generators and only one central makeup assembly. 2 figs.

DeFord, H.S.; Clark, M.L.

1981-11-03T23:59:59.000Z

152

E-Print Network 3.0 - aerosol pool scrubbing Sample Search Results  

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

sensing of non-aerosol absorption in cloud free atmosphere Yoram J. Kaufman,1 Summary: Remote sensing of non-aerosol absorption in cloud free atmosphere Yoram J. Kaufman,1 Oleg...

153

E-Print Network 3.0 - arctic aerosol burden Sample Search Results  

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

and surface... generally exhibits low aerosol ... Source: National Oceanic and Atmospheric Administration, Pacific Marine Environmental Laboratory, Atmopsheric Chemistry and...

154

E-Print Network 3.0 - aerosol sellest rgivad Sample Search Results  

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

October 4, 2004 Abstract Atmospheric aerosol particles scatter and absorb shortwave (solar) radiation and Source: Brookhaven National Laboratory, Environmental Chemistry...

155

E-Print Network 3.0 - aerosol biokinetics concentrations Sample...  

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

October 4, 2004 Abstract Atmospheric aerosol particles scatter and absorb shortwave (solar) radiation and Source: Brookhaven National Laboratory, Environmental Chemistry...

156

E-Print Network 3.0 - aerosols Sample Search Results  

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

October 4, 2004 Abstract Atmospheric aerosol particles scatter and absorb shortwave (solar) radiation and Source: Brookhaven National Laboratory, Environmental Chemistry...

157

Hyperspectral Aerosol Optical Depths from TCAP Flights  

SciTech Connect (OSTI)

4STAR (Spectrometer for Sky-Scanning, Sun-Tracking Atmospheric Research), the worlds 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 4STARs spatially-resolved high-frequency hyperspectral products as a reliable tool for climate studies and satellite validation.

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.

2013-11-13T23:59:59.000Z

158

EMSL - aerosols  

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

aerosols en Magnesium behavior and structural defects in Mg+ ion implanted silicon carbide. http:www.emsl.pnl.govemslwebpublicationsmagnesium-behavior-and-structural-defects-m...

159

Climate Sciences: Atmospheric Thermodynamics  

E-Print Network [OSTI]

1 Climate Sciences: Atmospheric Thermodynamics Instructor: Lynn Russell, NH343 http://aerosol.ucsd.edu/courses.html Text: Curry & Webster Atmospheric Thermodynamics Ch1 Composition Ch2 Laws Ch3 Transfers Ch12 Energy Climate Sciences: Atmospheric Thermodynamics Instructor: Lynn Russell, NH343 http

Russell, Lynn

160

Iron Speciation and Mixing in Single Aerosol Particles from the...  

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

iron from atmospheric aerosol is an essential nutrient that can control oceanic productivity, thereby impacting the global carbon budget and climate. Particles collected on...

Note: This page contains sample records for the topic "aerosols atmospheric profiling" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


161

aerosol monitor development: Topics by E-print Network  

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

Paris May 2003John Matthews Monitoring the Aerosol Phase Function University of New Mexico 12;AstroParticles & Atmosphere, Paris May 2003John Matthews 12;AstroParticles &...

162

Aerosols, Clouds, and Climate Change Stephen E. Schwartz  

E-Print Network [OSTI]

in atmospheric carbon dioxide associated with fossil fuel combustion. Briefly the options are mitigation work has shown instances of large magnitude of aerosol indirect forcing, with local instantaneous

Schwartz, Stephen E.

163

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)

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.

Lynn M. Russell; Richard C.J. Somerville

2012-11-05T23:59:59.000Z

164

Heterogeneous chemistry of atmospheric mineral dust particles and their resulting cloud-nucleation properties  

E-Print Network [OSTI]

Aerosol size distribution The size of an aerosol particle is an important parameter that controls the rates of diffusion, coagulation,coagulation into the larger ultrafine and accumulation Figure 1.1. Typical size distribution of atmospheric aerosols and

Sullivan, Ryan Christopher

2008-01-01T23:59:59.000Z

165

Modal Bin Hybrid Model: A Surface Area Consistent, Triple Moment Sectional Method for Use in Process-oriented Modeling of Atmospheric Aerosols  

SciTech Connect (OSTI)

A triple moment sectional method, Modal Bin Hybrid Model (MBHM), has been developed. In addition to number and mass (volume), surface area is predicted (and preserved), which is important for gas-to-particle mass transfer and light extinction cross section. The performance of MBHM was evaluated against double moment sectional (DMS) methods with various size resolutions up to BIN256 (BINx: x is number of sections over three orders of magnitude in size, ?logD = 3/x) for simulating evolution of particles under simultaneously occurring nucleation, condensation and coagulation processes. Because MBHM gives a physically consistent form of the intra-sectional distributions, errors and biases of MBHM at BIN4-8 resolution were almost equivalent to those of DMS at BIN16-32 resolution for various important variables such as the moments Mk (k: 0, 2, 3), dMk/dt, and the number and volume of particles larger than a certain diameter. Another important feature of MBHM is that only a single bin is adequate to simulate full aerosol dynamics for particles whose size distribution can be approximated by a single lognormal mode. This flexibility is useful for process-oriented (multi category and/or mixing state) modeling: primary aerosols whose size parameters would not differ substantially in time and space can be expressed by a single or a small number of modes, whereas secondary aerosols whose size changes drastically from one to several hundred nanometers can be expressed by a number of modes. Added dimensions can be applied to MBHM to represent mixing state or photo-chemical age for aerosol mixing state studies.

Kajino, Mizuo; Easter, Richard C.; Ghan, Steven J.

2013-09-10T23:59:59.000Z

166

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

SciTech Connect (OSTI)

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.

Hostetler, Chris; Ferrare, Richard

2013-02-14T23:59:59.000Z

167

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

E-Print Network [OSTI]

AEROSOL CHEMICAL COMPOSITION CHARACTERIZATION AT THE ARM SOUTHERN GREAT PLAINS (SGP) SITE USING AN AEROSOL CHEMICAL SPECIATION MONITOR Yin-Nan Lee1 , Fan Mei1 , Stephanie DeJong1 , Anne Jefferson2 1 Atmospheric Sciences Division, Brookhaven National Lab, Upton, NY 2 CIRES, University of Colorado, Boulder, CO

168

Lidar determination of altitude profile of the refraction index in electro-optical monitoring of the Earths atmosphere  

E-Print Network [OSTI]

generated data 1. Introduction Control of atmosphere pollution is a complex problem of environmental of the reconstruction of the individual contributions and the overall altitude pro- file of the refraction index of air the pollutants and obtain detailed information about the distri- bution of the substances both in altitude

169

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]

emissions from livestock have been documented as a significant regional, national, and global source of methane _____________ This dissertation follows the style of Atmospheric Environment. *Reprinted with permission from ?Using environmental scanning..., 1993) and tandem differential mobility analyzers, (Cruz and Pandis, 2000). The Environmental Scanning Electron Microscope (ESEM) technique employed here was previously used by Ebert et al. (2002) and Krueger et al. (2003). The ESEM has two specific...

Moon, Seong-Gi

2011-08-08T23:59:59.000Z

170

Investigation of the aerosol-cloud interaction using the WRF framework  

E-Print Network [OSTI]

. Simulations with various aerosol profiles demonstrate that the response of precipitation to the increase of aerosol concentrations is non-monotonic. The maximal cloud cover, core updraft, and maximal vertical velocity exhibit similar responses as precipitation...

Li, Guohui

2009-05-15T23:59:59.000Z

171

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

SciTech Connect (OSTI)

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.

Richard A. Ferrare; David D. Turner

2011-09-01T23:59:59.000Z

172

AEROSOL, CLOUDS, AND CLIMATE CHANGE  

SciTech Connect (OSTI)

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

SCHWARTZ, S.E.

2005-09-01T23:59:59.000Z

173

Technical Note: Estimating Aerosol Effects on Cloud Radiative Forcing  

SciTech Connect (OSTI)

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

Ghan, Steven J.

2013-10-09T23:59:59.000Z

174

Atmospheric Pb deposition since the Industrial Revolution recorded by five Swiss peat profiles: Enrichment factors, fluxes, isotopic composition, and sources  

SciTech Connect (OSTI)

Atmospheric Pb deposition since the Industrial Revolution was studied in western, central, and southern Switzerland using five rural peat bogs. Similar temporal patterns were found in western and central Switzerland, with two distinct periods of Pb enrichment relative to the natural background: between 1880 and 1920 with enrichments ranging from 40 to 80 times, and between 1960 and 1980 with enrichments ranging from 80 to 100 times. The fluxes also were generally elevated in those time periods: in western Switzerland between 1.16 and 1.55 {micro}g cm{sup {minus}2} y{sup {minus}1} during the second period. Between the Industrial Revolution and 1985, nonradiogenic Pb became increasingly important in all five cores because of the replacement of coal by oil after ca. 1920, the use of Australian Pb in industry, and the extensive combustion of leaded gasoline after 1950. The introduction of unleaded gasoline in 1985 had a pronounced effect on the Pb deposition in all five cores. Enrichments dropped sharply, and the isotopic ratios reverted back toward natural values. The cores from western and central Switzerland showed very similar isotopic trends throughout the time period studied, implying that these sites were influenced contemporaneously by similar pollution sources and atmospheric pathways. Southern Switzerland revealed a different record with respect to the Pb pollution: it was dominated by a single massive Pb enrichment dated between 1930 and 1950.

Weiss, D.; Shotyk, W.; Kramers, J.D. [Univ. of Bern (Switzerland)] [Univ. of Bern (Switzerland); Appleby, P.G. [Univ. of Liverpool (United Kingdom). Dept. of Mathematical Sciences] [Univ. of Liverpool (United Kingdom). Dept. of Mathematical Sciences; Cheburkin, A.K. [Ukrainian Academy of Sciences, Kiev (Ukraine). Inst. of Geological Sciences] [Ukrainian Academy of Sciences, Kiev (Ukraine). Inst. of Geological Sciences

1999-05-01T23:59:59.000Z

175

E-Print Network 3.0 - atmosphere part ii Sample Search Results  

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

particles (Duce, 2005). Atmospheric... and thus influence atmospheric carbon dioxide con- centrations and climate. As a result, studies of aerosol... in surface waters of...

176

E-Print Network 3.0 - atmospheric material particles Sample Search...  

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

MECHANICAL AND AEROSPACE ENGINEERING COLLOQUIUM SERIES Atmospheric Aerosols: Linking Air Pollution... Earth's atmosphere with sulfur to cool down the earth? Is this true that...

177

E-Print Network 3.0 - atmospheric pollution part Sample Search...  

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

MECHANICAL AND AEROSPACE ENGINEERING COLLOQUIUM SERIES Atmospheric Aerosols: Linking Air Pollution... Earth's atmosphere with sulfur to cool down the earth? Is this true that...

178

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.

179

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

SciTech Connect (OSTI)

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.

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

2014-08-01T23:59:59.000Z

180

E-Print Network 3.0 - aerosol concentration enrichment Sample...  

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

observed aerosol170 ... Source: Heald, Colette L. - Department of Atmospheric Science, Colorado State University Collection: Environmental Sciences and Ecology ; Geosciences 57...

Note: This page contains sample records for the topic "aerosols atmospheric profiling" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


181

E-Print Network 3.0 - aerosol direct radiative Sample Search...  

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

Transfer Encyclopedia of Atmospheric Science William D. Collins... system. Naturally occurring aerosols reflect some of the incident solar radiation back to space before... the...

182

E-Print Network 3.0 - annually occurring aerosol Sample Search...  

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

in Radiative Transfer Encyclopedia of Atmospheric Science Summary: system. Naturally occurring aerosols reflect some of the incident solar radiation back to space before... in...

183

E-Print Network 3.0 - aerosol generators Sample Search Results  

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

Dodd Way, Atlanta, GA, 30332, U.S.A. Abstract. Atmospheric aerosols scatter and absorb solar Source: Bergin, Mike - Schools of Civil and Environmental Engineering & Earth and...

184

E-Print Network 3.0 - aerosol monitoring Sample Search Results  

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

Dodd Way, Atlanta, GA, 30332, U.S.A. Abstract. Atmospheric aerosols scatter and absorb solar Source: Bergin, Mike - Schools of Civil and Environmental Engineering & Earth and...

185

E-Print Network 3.0 - aerosol size classification Sample Search...  

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

Imaging Spectroradiometer observations: Top-of-atmosphere albedo change Summary: Panel on Climate Change, 2007. Aerosol particles have a variety of shapes, sizes, and...

186

E-Print Network 3.0 - aerosol retrieval algorithms Sample Search...  

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

the scavenging... site provide retrievals of aerosol, cloud, precipitation and radiative heating in the Arctic? 12;Key... profiles derived from ground-based and satellite remote...

187

FY 2010 Third Quarter Report Comparison of Aerosol and Cloud Condensation Nuclei (CCN) Relationship Parameterizations with Data Collected During the 2008 VAMOS Ocean-Cloud-Atmosphere Land Study (VOCALS) Field Campaign  

SciTech Connect (OSTI)

Metric for Quarter 3: Report comparisons of aerosol/CCN relationship parameterizations with data collected in the first quarter and best parameterization for VOCALS data set.

Wang, J; Daum, PH; Kleinman, LI; Lee, YN; McGraw, R; Sedlacek, AJ; Senum, G; Springston, SR

2010-06-01T23:59:59.000Z

188

Emerging Issues in Nanoparticle Aerosol Science and Technology Workshop report sponsored by: NSF, Southern California Particle Center and UCLA  

E-Print Network [OSTI]

has responsibility for nuclear reactor safety which includes emissions of radioactive particles pollution sources, (2) industrial production of nanoparticle reinforcing fillers such as carbon black nanoparticle products by aerosol processes, (4) atmospheric dynamics of fractal-like nanoparticle aerosols (e

Jimenez, Jose-Luis

189

atmosphere gcm implications: Topics by E-print Network  

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

gases, and sulfate aerosols are predicted to raise global temperatures via the "greenhouse effect" (IPCC, 1996), growing emissions of SO2Interactions Among Emissions, Atmospheric...

190

Atmospheric optical calibration system  

DOE Patents [OSTI]

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.

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

1988-10-25T23:59:59.000Z

191

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

SciTech Connect (OSTI)

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.

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

2009-03-05T23:59:59.000Z

192

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

SciTech Connect (OSTI)

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.

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

2007-09-30T23:59:59.000Z

193

Aerosol-Cloud interactions : a new perspective in precipitation enhancement  

E-Print Network [OSTI]

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 ...

Gunturu, Udaya Bhaskar

2010-01-01T23:59:59.000Z

194

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

E-Print Network [OSTI]

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 ...

Alvarado, Matthew James

2008-01-01T23:59:59.000Z

195

Phase transformation and growth of hygroscopic aerosols  

SciTech Connect (OSTI)

Ambient aerosols play an important role in many atmospheric processes affecting air quality, visibility degradation, and climatic changes as well. Both natural and anthropogenic sources contribute to the formation of ambient aerosols, which are composed mostly of sulfates, nitrates, and chlorides in either pure or mixed forms. These inorganic salt aerosols are hygroscopic by nature and exhibit the properties of deliquescence and efflorescence in humid air. For pure inorganic salt particles with diameter larger than 0.1 micron, the phase transformation from a solid particle to a saline droplet occurs only when the relative humidity in the surrounding atmosphere reaches a certain critical level corresponding to the water activity of the saturated solution. The droplet size or mass in equilibrium with relative humidity can be calculated in a straightforward manner from thermodynamic considerations. For aqueous droplets 0.1 micron or smaller, the surface curvature effect on vapor pressure becomes important and the Kelvin equation must be used.

Tang, I.N.

1999-11-01T23:59:59.000Z

196

3, 59195976, 2003 The nitrate aerosol  

E-Print Network [OSTI]

ACPD 3, 5919­5976, 2003 The nitrate aerosol field over Europe M. Schaap et al. Title Page Abstract of Utrecht, Institute of Marine and Atmospheric Science, PO Box 80005, 3508 TA, Utrecht, The Netherlands 2, The Netherlands 3 Netherlands Energy Research Foundation (ECN), PO Box 1, 1755 LE Petten, The Netherlands 4 Joint

Paris-Sud XI, Université de

197

Improved solid aerosol generator  

DOE Patents [OSTI]

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.

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

1988-07-19T23:59:59.000Z

198

Characterizing the formation of secondary organic aerosols  

SciTech Connect (OSTI)

Organic aerosol is an important fraction of the fine particulate matter present in the atmosphere. This organic aerosol comes from a variety of sources; primary organic aerosol emitted directly from combustion process, and secondary aerosol formed in the atmosphere from condensable vapors. This secondary organic aerosol (SOA) can result from both anthropogenic and biogenic sources. In rural areas of the United States, organic aerosols can be a significant part of the aerosol load in the atmosphere. However, the extent to which gas-phase biogenic emissions contribute to this organic load is poorly understood. Such an understanding is crucial to properly apportion the effect of anthropogenic emissions in these rural areas that are sometimes dominated by biogenic sources. To help gain insight on the effect of biogenic emissions on particle concentrations in rural areas, we have been conducting a field measurement program at the University of California Blodgett Forest Research Facility. The field location includes has been used to acquire an extensive suite of measurements resulting in a rich data set, containing a combination of aerosol, organic, and nitrogenous species concentration and meteorological data with a long time record. The field location was established in 1997 by Allen Goldstein, a professor in the Department of Environmental Science, Policy and Management at the University of California at Berkeley to study interactions between the biosphere and the atmosphere. The Goldstein group focuses on measurements of concentrations and whole ecosystem biosphere-atmosphere fluxes for volatile organic compounds (VOC's), oxygenated volatile organic compounds (OVOC's), ozone, carbon dioxide, water vapor, and energy. Another important collaborator at the Blodgett field location is Ronald Cohen, a professor in the Chemistry Department at the University of California at Berkeley. At the Blodgett field location, his group his group performs measurements of the concentrations of important gas phase nitrogen compounds. Experiments have been ongoing at the Blodgett field site since the fall of 2000, and have included portions of the summer and fall of 2001, 2002, and 2003. Analysis of both the gas and particle phase data from the year 2000 show that the particle loading at the site correlates with both biogenic precursors emitted in the forest and anthropogenic precursors advected to the site from Sacramento and the Central Valley of California. Thus the particles at the site are affected by biogenic processing of anthropogenic emissions. Size distribution measurements show that the aerosol at the site has a geometric median diameter of approximately 100 nm. On many days, in the early afternoon, growth of nuclei mode particles (<20 nm) is also observed. These growth events tend to occur on days with lower average temperatures, but are observed throughout the summer. Analysis of the size resolved data for these growth events, combined with typical measured terpene emissions, show that the particle mass measured in these nuclei mode particles could come from oxidation products of biogenic emissions, and can serve as a significant route for SOA partitioning into the particle phase. During periods of each year, the effect of emissions for forest fires can be detected at the Blodgett field location. During the summer of 2002 emissions from the Biscuit fire, a large fire located in Southwest Oregon, was detected in the aerosol data. The results show that increases in particle scattering can be directly related to increased black carbon concentration and an appearance of a larger mode in the aerosol size distribution. These results show that emissions from fires can have significant impact on visibility over large distances. The results also reinforce the view that forest fires can be a significant source of black carbon in the atmosphere, which has important climate and visibility. Continuing work with the 2002 data set, particularly the combination of the aerosol and gas phase data, will continue to provide important information o

Lunden, Melissa; Black, Douglas; Brown, Nancy

2004-02-01T23:59:59.000Z

199

Toxicity of atmospheric aerosols on marine phytoplankton  

E-Print Network [OSTI]

fertilization on carbon sequestration in the Southern Ocean.production, and carbon sequestration (47). In areas whereproductivity and carbon sequestration and thus influence

2009-01-01T23:59:59.000Z

200

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May JunDatastreamsmmcrcalgovInstrumentsruc DocumentationP-Series to User Group and UserofProteinNewsatCompilerMarch-25,-2015

Note: This page contains sample records for the topic "aerosols atmospheric profiling" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


201

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May JunDatastreamsmmcrcalgovInstrumentsruc DocumentationP-Series to User Group and UserofProteinNewsatCompilerMarch-25,-2015Composition and

202

Aerodynamic size associations of natural radioactivity with ambient aerosols  

SciTech Connect (OSTI)

The aerodynamic size of /sup 214/Pb, /sup 212/Pb, /sup 210/Pb, /sup 7/Be, /sup 32/P, /sup 35/S (as SO/sub 4//sup 2 -/), and stable SO/sub 4//sup 2 -/ was measured using cascade impactors. The activity distribution of /sup 212/Pb and /sup 214/Pb, measured by alpha spectroscopy, was largely associated with aerosols smaller than 0.52 ..mu..m. Based on 46 measurements, the activity median aerodynamic diameter of /sup 212/Pb averaged 0.13 ..mu..m (sigma/sub g/ = 2.97), while /sup 214/Pb averaged 0.16 ..mu..m (sigma/sub g/ = 2.86). The larger median size of /sup 214/Pb was attributed to ..cap alpha..-recoil depletion of smaller aerosols following decay of aerosol-associated /sup 218/Po. Subsequent /sup 214/Pb condensation on all aerosols effectively enriches larger aerosols. /sup 212/Pb does not undergo this recoil-driven redistribution. Low-pressure impactor measurements indicated that the mass median aerodynamic diameter of SO/sub 4//sup 2 -/ was about three times larger than the activity median diameter /sup 212/Pb, reflecting differences in atmospheric residence times as well as the differences in surface area and volume distributions of the atmospheric aerosol. Cosmogenic radionuclides, especially /sup 7/Be, were associated with smaller aerosols than SO/sub 4//sup 2 -/ regardless of season, while /sup 210/Pb distributions in summer measurements were similar to sulfate but smaller in winter measurements. Even considering recoil following /sup 214/Po ..cap alpha..-decay, the avervage /sup 210/Pb labeled aerosol grows by about a factor of two during its atmospheric lifetime. The presence of 5 to 10% of the /sup 7/Be on aerosols greater than 1 ..mu..m was indicative of post-condensation growth, probably either in the upper atmosphere or after mixing into the boundary layer.

Bondietti, E.A.; Papastefanou, C.; Rangarajan, C.

1986-04-01T23:59:59.000Z

203

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]

are an programs dealing with atmospheric science, subsurface science, environmental radon, ocean margins Division, the Atmospheric Radiation Measurement (ARM) Program and the Atmospheric Chemistry Program (ACP--Atmospheric Radiation Measurement Program. The ARM Program is the Department's major research activity focusing

204

Pressure-flow reducer for aerosol focusing devices  

DOE Patents [OSTI]

A pressure-flow reducer, and an aerosol focusing system incorporating such a pressure-flow reducer, for performing high-flow, atmosphere-pressure sampling while delivering a tightly focused particle beam in vacuum via an aerodynamic focusing lens stack. The pressure-flow reducer has an inlet nozzle for adjusting the sampling flow rate, a pressure-flow reduction region with a skimmer and pumping ports for reducing the pressure and flow to enable interfacing with low pressure, low flow aerosol focusing devices, and a relaxation chamber for slowing or stopping aerosol particles. In this manner, the pressure-flow reducer decouples pressure from flow, and enables aerosol sampling at atmospheric pressure and at rates greater than 1 liter per minute.

Gard, Eric (San Francisco, CA); Riot, Vincent (Oakland, CA); Coffee, Keith (Diablo Grande, CA); Woods, Bruce (Livermore, CA); Tobias, Herbert (Kensington, CA); Birch, Jim (Albany, CA); Weisgraber, Todd (Brentwood, CA)

2008-04-22T23:59:59.000Z

205

Residence times of fine tropospheric aerosols as determined by {sup 210}Pb progeny.  

SciTech Connect (OSTI)

Fine tropospheric aerosols can play important roles in the radiative balance of the atmosphere. The fine aerosols can act directly to cool the atmosphere by scattering incoming solar radiation, as well as indirectly by serving as cloud condensation nuclei. Fine aerosols, particularly carbonaceous soots, can also warm the atmosphere by absorbing incoming solar radiation. In addition, aerosols smaller than 2.5 {micro}m have recently been implicated in the health effects of air pollution. Aerosol-active radioisotopes are ideal tracers for the study of atmospheric transport processes. The source terms of these radioisotopes are relatively well known, and they are removed from the atmosphere only by radioactive decay or by wet or dry deposition of the host aerosol. The progeny of the primordial radionuclide {sup 238}U are of particular importance to atmospheric studies. Uranium-238 is common throughout Earth's crust and decays to the inert gas {sup 222}Rn, which escapes into the atmosphere. Radon-222 decays by the series of alpha and beta emissions shown in Figure 1 to the long-lived {sup 210}Pb. Once formed, {sup 210}Pb becomes attached to aerosol particles with average attachment times of 40 s to 3 min.

Marley, N. A.; Gaffney, J. S.; Drayton, P. J.; Cunningham, M. M.; Mielcarek, C.; Ravelo, R.; Wagner, C.

1999-10-05T23:59:59.000Z

206

E-Print Network 3.0 - atmospheric surface layer Sample Search...  

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

determining albedo and opacity Clouds Snow and ice Aerosols Time... Horizontal transport in the atmosphere Dry and moist static energy Eddy ... Source: Sherwood, Steven -...

207

E-Print Network 3.0 - atmospherically derived pb Sample Search...  

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

on leaded gasoline usage, aerosols in remote regions... long-term histories of atmospheric Pb pollution ... Source: Wolfe, Alexander P. - Department of Earth and...

208

E-Print Network 3.0 - atmospheric monitoring mass Sample Search...  

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

Paris May 2003John Matthews Monitoring the Aerosol Phase Function... University of New Mexico 12;AstroParticles & Atmosphere, Paris May 2003John Matthews 12;Astro... Particles &...

209

Simulation of aerosol dynamics: a comparative review of mathematical models  

SciTech Connect (OSTI)

Three modeling approaches used are based-continuous, discrete (sectional), and parameterized representations of the aerosol size distribution. Simulations of coagulation and condensation are performed with the three models for clear, hazy, and urban atmospheric conditions. Relative accuracies and computational costs are compared. Reference for the comparison is the continuous approach. The results of the study provide useful information for the selection of an aerosol model, depending on the accuracy requirements and computational constraints associated with a specific application.

Seigneur, C.; Hudischewskyj, A.B.; Seinfeld, J.H.; Whitby, K.T.; Whitby, E.R.

1986-01-01T23:59:59.000Z

210

The Aerosol Modeling Testbed: A community tool to objectively evaluate aerosol process modules  

SciTech Connect (OSTI)

This study describes a new modeling paradigm that significantly advances how the third activity is conducted while also fully exploiting data and findings from the first two activities. The Aerosol Modeling Testbed (AMT) is a computational framework for the atmospheric sciences community that streamlines the process of testing and evaluating aerosol process modules over a wide range of spatial and temporal scales. The AMT consists of a fully-coupled meteorology-chemistry-aerosol model, and a suite of tools to evaluate the performance of aerosol process modules via comparison with a wide range of field measurements. The philosophy of the AMT is to systematically and objectively evaluate aerosol process modules over local to regional spatial scales that are compatible with most field campaigns measurement strategies. The performance of new treatments can then be quantified and compared to existing treatments before they are incorporated into regional and global climate models. Since the AMT is a community tool, it also provides a means of enhancing collaboration and coordination among aerosol modelers.

Fast, Jerome D.; Gustafson, William I.; Chapman, Elaine G.; Easter, Richard C.; Rishel, Jeremy P.; Zaveri, Rahul A.; Grell, Georg; Barth, Mary

2011-03-02T23:59:59.000Z

211

Direct and semidirect aerosol effects of Southern African biomass burning aerosol  

SciTech Connect (OSTI)

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.

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

2011-06-21T23:59:59.000Z

212

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)

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.

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

2011-08-31T23:59:59.000Z

213

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

SciTech Connect (OSTI)

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.

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.

1995-09-27T23:59:59.000Z

214

Aerosol Working Group Contributions Accomplishments for 2006  

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth (AOD)ProductssondeadjustsondeadjustAbout the BuildingInnovation 2011 Simulation StudiesAerosol

215

Broadband Heating Rate Profile Project (BBHRP) - SGP ripbe370mcfarlane  

SciTech Connect (OSTI)

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.

Riihimaki, Laura; Shippert, Timothy

2014-11-05T23:59:59.000Z

216

Broadband Heating Rate Profile Project (BBHRP) - SGP ripbe1mcfarlane  

SciTech Connect (OSTI)

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.

Riihimaki, Laura; Shippert, Timothy

2014-11-05T23:59:59.000Z

217

Broadband Heating Rate Profile Project (BBHRP) - SGP ripbe1mcfarlane  

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

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.

Riihimaki, Laura; Shippert, Timothy

218

Broadband Heating Rate Profile Project (BBHRP) - SGP ripbe370mcfarlane  

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

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.

Riihimaki, Laura; Shippert, Timothy

219

Thermophoretic separation of aerosol particles from a sampled gas stream  

SciTech Connect (OSTI)

A method is described for separating aerosol particles from a gas sample being withdrawn from a contained atmosphere, comprising the following steps: placing within the contained atmosphere a covering gas impermeable enclosure have an interior chamber partly defined by a bottom metal plate that is permeable to gas; fixing the position of the enclosure with the plate facing downwardly and directly exposed to the contained atmosphere; heating the metal plate to a temperature greater than that of the contained atmosphere, whereby aerosol particles are repelled to the resulting thermophoretic forces applied to them by the temperature gradient produced in the atmosphere immediately under the plate; and sampling gas within the interior chamber of the enclosure.

Poztman, A.K.

1986-02-25T23:59:59.000Z

220

Organic Aerosols in the Earth's J O O S T D E G O U W *  

E-Print Network [OSTI]

, and indirectly through their role as cloud-condensation nuclei. A large fraction (50%) of the submicron aerosol(primaryorganicaerosolorPOA) are distinguished from secondary organic aerosol (SOA) formed in the atmosphere from gas-phase precursors. Both POA scales of minutes: particle-into-liquid sampling combined with total organic carbon analysis for measure

Jimenez, Jose-Luis

Note: This page contains sample records for the topic "aerosols atmospheric profiling" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


221

GOME-2 ABSORBING AEROSOL INDEX: STATISTICAL ANALYSIS, COMPARISON TO GOME-1 AND IMPACT OF INSTRUMENT  

E-Print Network [OSTI]

DEGRADATION Lieuwe G. Tilstra, Olaf N.E. Tuinder, and Piet Stammes Royal Netherlands Meteorological Institute the presence of UV-absorbing aerosols. These aerosols are mainly injected into the atmosphere by desert dust that the GOME-2 AAI product is suffering more and more from the effects of instrument degradation. In particular

Tilstra, Gijsbert

222

Generation and characterization of radiolabelled nanosized carbonaceous aerosols for human inhalation studies  

E-Print Network [OSTI]

and the aerosol residence time were the main parameters influencing15 the particle size distribution. Under-fractionation and gamma-scintigraphy detection to7 determine the aerosol aerodynamic-related distributions. It was found in an atmosphere of pure argon.34 The number size distribution of Technegas particles is mainly below 100 nm (Vita

Boyer, Edmond

223

Thermophoretic separation of aerosol particles from a sampled gas stream  

SciTech Connect (OSTI)

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.

Postma, Arlin K. (Halfway, OR)

1986-01-01T23:59:59.000Z

224

Modal aerosol dynamics modeling  

SciTech Connect (OSTI)

The report presents the governing equations for representing aerosol dynamics, based on several different representations of the aerosol size distribution. Analytical and numerical solution techniques for these governing equations are also reviewed. Described in detail is a computationally efficient numerical technique for simulating aerosol behavior in systems undergoing simultaneous heat transfer, fluid flow, and mass transfer in and between the gas and condensed phases. The technique belongs to a general class of models known as modal aerosol dynamics (MAD) models. These models solve for the temporal and spatial evolution of the particle size distribution function. Computational efficiency is achieved by representing the complete aerosol population as a sum of additive overlapping populations (modes), and solving for the time rate of change of integral moments of each mode. Applications of MAD models for simulating aerosol dynamics in continuous stirred tank aerosol reactors and flow aerosol reactors are provided. For the application to flow aerosol reactors, the discussion is developed in terms of considerations for merging a MAD model with the SIMPLER routine described by Patankar (1980). Considerations for incorporating a MAD model into the U.S. Environmental Protection Agency's Regional Particulate Model are also described. Numerical and analytical techniques for evaluating the size-space integrals of the modal dynamics equations (MDEs) are described. For multimodal logonormal distributions, an analytical expression for the coagulation integrals of the MDEs, applicable for all size regimes, is derived, and is within 20% of accurate numerical evaluation of the same moment coagulation integrals. A computationally efficient integration technique, based on Gauss-Hermite numerical integration, is also derived.

Whitby, E.R.; McMurry, P.H.; Shankar, U.; Binkowski, F.S.

1991-02-01T23:59:59.000Z

225

Microphysical modeling of ultrane hydrocarbon-containing aerosols in aircraft emissions  

E-Print Network [OSTI]

Combustion engines emit precursors of ne particulate matter (PM) into the atmosphere. Numerous gaseous species, soot particles, and liquid aerosols in the aircraft exhaust are involved in PM formation, and these very ne, ...

Jun, Mina

2011-01-01T23:59:59.000Z

226

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

E-Print Network [OSTI]

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 ...

Cziczo, Daniel James

227

Contrasting the direct radiative effect and direct radiative forcing of aerosols  

E-Print Network [OSTI]

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 ...

Heald, Colette L.

228

Aerosol Cans? -Aerosol cans use a pressurized  

E-Print Network [OSTI]

? - The waste generated in the processing of images/photos contains silver. Silver is a toxic heavy metal the product. Propellants are often flammable and/or toxic. Therefore, never store aerosol cans near ignition of this pamphlet. -Carefully transfer the old paint thinner from the one gallon closable can to the 30 gallon metal

Jia, Songtao

229

Acidbase chemical reaction model for nucleation rates in the polluted atmospheric boundary layer  

E-Print Network [OSTI]

Atmospheric Sciences Division, Brookhaven National Laboratory, Upton, NY 11973; f Sustainable Energy Systems Group, Environmental Energy Technologies Division, E. O. Lawrence Berkeley National Laboratory, Berkeley agreement with measurements from Mexico City and Atlanta. amines | atmospheric aerosol | climate forcing

230

Measuring Nighttime Atmospheric Opacity Using Images From the Mars Exploration Rovers  

E-Print Network [OSTI]

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...

Bean, Keri M

2012-07-11T23:59:59.000Z

231

The Ability of MM5 to Simulate Ice Clouds: Systematic Comparison between Simulated and Measured Fluxes and Lidar/Radar Profiles at SIRTA Atmospheric Observatory  

SciTech Connect (OSTI)

Ice clouds play a major role in the radiative energy budget of the Earth-atmosphere system (Liou 1986). Their radiative effect is governed primarily by the equilibrium between their albedo and greenhouse effects. Both macrophysical and microphysical properties of ice clouds regulate this equilibrium. For quantifying the effect of these clouds onto climate and weather systems, they must be properly characterized in atmospheric models. In this paper we use remote-sensing measurements from the SIRTA ground based atmospheric observatory (Site Instrumental de Recherche par Teledetection Atmospherique, http://sirta.lmd.polytechnique.fr). Lidar and radar observations taken over 18 months are used, in order to gain statistical confidence in the model evaluation. Along this period of time, 62 days are selected for study because they contain parts of ice clouds. We use the ''model to observations'' approach by simulating lidar and radar signals from MM5 outputs. Other more classical variables such as shortwave and longwave radiative fluxes are also used. Four microphysical schemes, among which that proposed by Reisner et al. (1998) with original or modified parameterizations of particle terminal fall velocities (Zurovac-Jevtic and Zhang 2003, Heymsfield and Donner 1990), and the simplified Dudhia (1989) scheme are evaluated in this study.

Chiriaco, M.; Vautard, R.; Chepfer, H.; Haeffelin, M.; Wanherdrick, Y.; Morille, Y.; Protat, A.; Dudhia, J.

2005-03-18T23:59:59.000Z

232

The Two-Column Aerosol Project (TCAP) Science Plan  

SciTech Connect (OSTI)

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.

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

2011-07-27T23:59:59.000Z

233

Influence of clouds and diffuse radiation on ecosystem-atmosphere CO 2 and CO 18 O exchanges  

E-Print Network [OSTI]

cover, radiation, meteorological and water isotope data tohere, radiation, cloud property, and aerosol data wereData were obtained from the Atmospheric Radiation

2009-01-01T23:59:59.000Z

234

Aerosol Sampler Operations Manual  

E-Print Network [OSTI]

-1123 Laboratory FAX (916) 752-4107 Standard Operating Procedures Technical Information Document TI 201A #12;TI 201.................................................................................................................................................. 3 1.0 Weekly Maintenance ProceduresIMPROVE Aerosol Sampler Operations Manual February 10, 1997 Air Quality Group Crocker Nuclear

Fischer, Emily V.

235

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

SciTech Connect (OSTI)

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.

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

2014-05-13T23:59:59.000Z

236

Speciation of Fe in ambient aerosol and cloudwater  

SciTech Connect (OSTI)

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.

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

1996-08-15T23:59:59.000Z

237

Correction to Hyperspectral Aerosol Optical Depths from TCAP Flights  

SciTech Connect (OSTI)

In the paper Hyperspectral aerosol optical depths from TCAP flights by Y. Shinozuka et al. (Journal of Geophysical Research: Atmospheres, 118, doi:10.1002/2013JD020596, 2013), Tables 1 and 2 were published with the column heads out of order. Tables 1 and 2 are published correctly here. The publisher regrets the error.

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.

2014-02-16T23:59:59.000Z

238

Water content and morphology of sodium chloride aerosol particles  

E-Print Network [OSTI]

to explain the H2O content. The model in which the NaCl particles contain pockets of aqueous NaCl solution was found to be most consistent with the spectroscopic observations. The relevance of salt particle morphology and water content to atmospheric aerosol...

Weis, David D.; Ewing, George E.

1999-09-20T23:59:59.000Z

239

Aerosol Retrievals from ARM SGP MFRSR Data  

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

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.

Alexandrov, Mikhail

240

5, 79658026, 2005 Simulating aerosol  

E-Print Network [OSTI]

composition, number concentration, and size distribution of the global submicrometer aerosol. The present, coagulation, condensation, nucleation of sulfuric acid vapor, aerosol chemistry, cloud processing, and sizeACPD 5, 7965­8026, 2005 Simulating aerosol microphysics with ECHAM/MADE A. Lauer et al. Title Page

Paris-Sud XI, Université de

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they are not comprehensive nor are they the most current set.
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241

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

SciTech Connect (OSTI)

The climatic effects of dust aerosols in North Africa have been investigated using the atmospheric general circulation model (AGCM) developed at the University of California, Los Angeles (UCLA). The model includes an efficient and physically based radiation parameterization scheme developed specifically for application to clouds and aerosols. Parameterization of the effective ice particle size in association with the aerosol indirect effect based on cloud and aerosol data retrieved from A-Train satellite observations have been employed in the climate model simulations. Offline simulations reveal that the direct solar, IR, and net forcings by dust aerosols generally increase with increasing aerosol optical depth (AOD). When the dust semi-direct effect is included with the presence of ice clouds, positive IR radiative forcing is enhanced, since ice clouds trap substantial IR radiation, while the positive solar forcing with dust aerosols alone has been changed to negative values due to the strong reflection of solar radiation by clouds, indicating that cloud forcing could exceed aerosol forcing. With the aerosol indirect effect, the net cloud forcing is generally reduced for ice water path (IWP) larger than 20 g m-2. The magnitude of the reduction increases with IWP. AGCM simulations show that the reduced ice crystal mean effective size due to the aerosol first indirect effect result in less OLR and net solar flux at the top of the atmosphere over the cloudy area of the North Africa region because ice clouds with smaller size trap more IR radiation and reflect more solar radiation. The precipitation in the same area, however, increases due to the aerosol indirect effect on ice clouds, corresponding to the enhanced convection as indicated by reduced OLR. The increased precipitation seems to be associated with enhanced ice water contents in this region. The 200 mb radiative heating rate shows more cooling with the aerosol indirect effect since greater cooling is produced at the cloud top with smaller ice crystal size. The 500 mb omega indicates strong upward motion, which, together with the increased cooling effect, results in the increased ice water contents. Adding the aerosol direct effect into the model simulation reduces the precipitation in the normal rainfall band over North Africa, where precipitation is shifted to the south and the northeast produced by the absorption of sunlight and the subsequent heating of the air column by dust particles. As a result, rainfall is drawn further inland to the northeast. This study represents the first attempt to quantify the climate impact of aerosol indirect effect using a GCM in connection with A-train satellite data. The parameterization for the aerosol first indirect effect developed in this study can be readily incorporated for application to any other GCMs.

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

2012-02-15T23:59:59.000Z

242

Aerosol engineering: design and stability of aerosol reactors  

SciTech Connect (OSTI)

A theoretical study of the performance of aerosol reactors is presented. The goals of this study are (1) to identify the appropriate reactor types (batch, CSTR, and tubular) for production of aerosol with specific properties (for example, uniform size particles, high aerosol surface area, etc.) and (2) to investigate the effect of various process parameters on product aerosol characteristics and on the stability of operation of aerosol reactors. In all the reactors considered, the aerosol dynamics were detemined by chemical reaction, nucleation, and aerosol growth in the free molecule regime in the absence of coagulation at isothermal conditions. Formulation of the aerosol dynamics in terms of moments of the aerosol size distribution facilitated the numerical solution of the resulting systems of ordinary or partial differential equations. The stability characteristics of a continuous stirred tank aerosol reactor (CSTAR) were investigated since experimental data in the literature indicate that under certain conditions this reactor exhibits oscillatory behavior with respect to product aerosol concentration and size distribution.

Pratsinis, S.E.

1985-01-01T23:59:59.000Z

243

REPRESENTING AEROSOL DYNAMICS AND PROPERTIES IN CHEMICAL TRANSPORT MODELS BY THE METHOD OF MOMENTS.  

SciTech Connect (OSTI)

Atmospheric aerosols, suspensions of solid or liquid particles, are an important multi-phase system. Aerosols scatter and absorb shortwave (solar) radiation, affecting climate (Charlson et al., 1992; Schwartz, 1996) and visibility; nucleate cloud droplet formation, modifying the reflectivity of clouds (Twomey et al., 1984; Schwartz and Slingo, 1996) as well as contributing to composition of cloudwater and to wet deposition (Seinfeld and Pandis, 1998); and affect human health through inhalation (NRC, 1998). Existing and prospective air quality regulations impose standards on concentrations of atmospheric aerosols to protect human health and welfare (EPA, 1998). Chemical transport and transformation models representing the loading and geographical distribution of aerosols and precursor gases are needed to permit development of effective and efficient strategies for meeting air quality standards, and for examining aerosol effects on climate retrospectively and prospectively for different emissions scenarios. Important aerosol properties and processes depend on their size distribution: light scattering, cloud nucleating properties, dry deposition, and penetration into airways of lungs. The evolution of the mass loading itself depends on particle size because of the size dependence of growth and removal processes. For these reasons it is increasingly recognized that chemical transport and transformation models must represent not just the mass loading of atmospheric particulate matter but also the aerosol microphysical properties and the evolution of these properties if aerosols are to be accurately represented in these models. If the size distribution of the aerosol is known, a given property can be evaluated as the integral of the appropriate kernel function over the size distribution. This has motivated the approach of determining aerosol size distribution, and of explicitly representing this distribution and its evolution in chemical transport models.

SCHWARTZ,S.E.; MCGRAW,R.; BENKOVITZ,C.M.; WRIGHT,D.L.

2001-04-01T23:59:59.000Z

244

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmosphericNuclear Security AdministrationcontrollerNanocrystalline Gallium Oxide Thin Films.AdministrationAerosol Indirect

245

Aerosol Remote Sealing System - Energy Innovation Portal  

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth (AOD)ProductssondeadjustsondeadjustAbout the BuildingInnovation 2011 Simulation StudiesAerosol Remote Sealing

246

Dynamics of Planetary Atmospheres  

E-Print Network [OSTI]

pressure (bars) N2 82%; Ar 12%; CH4 6%CO2 96.5%; N2 3.5%Atmospheric composition 26177Orbital inclination (1992) orbiter ­ Winds from cloud-tracking and probe drifts ­ IR temperatures, solar-fixed tides, polar-Huygens mission (from 2005) ­ Doppler wind descent profile ­ IR temperature and composition maps ­ Visible, IR

Read, Peter L.

247

Thermophoretic separation of aerosol particles from a sampled gas stream  

DOE Patents [OSTI]

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.

Postma, A.K.

1984-09-07T23:59:59.000Z

248

Electrostatics and radioactive aerosol behavior  

SciTech Connect (OSTI)

Radioactive aerosols differ from their nonradioactive counterparts by their ability to charge themselves by emitting charged particles during the radioactive decay process. Evidence that electrostatics, including this charging process, can affect the transport of the aerosols was summarized previously. Charge distributions and the mean charge for a monodisperse radioactive aerosol have been considered in detail. The principal results of theory to calculate charge distributions on a aerosol with a size distribution, changes to Brownian coagulation rates for an aerosol in a reactor containment, and possible changes to aerosol deposition resulting from the charging will be presented. The main purpose of the work has been to improve calculations of aerosol behavior in reactor containments, but behavior in less ionizing environments will be affected more strongly, and some problems remain to be solved in performing reliable calculations.

Clement, C.F.

1994-12-31T23:59:59.000Z

249

aerosols and climate : uncertainties  

E-Print Network [OSTI]

contributes to creating a level playing field. (BC emissions tradeble like CO2 emissions?) OUTLINE #12;size. policy measures, is even more uncertain (emissions & their chemical fingerprint are uncertain (not just aerosol emissions, not just climate impacts) OUTLINE #12;- Standardization doesn't reduce

250

Where do particulate toxins reside? An improved paradigm for the structure and dynamics of the urban mid-Atlantic aerosol  

SciTech Connect (OSTI)

Discussions of excess mortality and morbidity from exposure to urban aerosol particles typically invoke the now 20-year-old trimodal aerosol paradigm proposed by Whitby to explain the structure and behavior of ambient aerosol volume and its major constituent, sulfate. However, this paradigm largely ignores the primary high-temperature combustion (HTC) components of the urban aerosol, which contribute minor amounts of the aerosol mass, but carry the bulk of the particulate toxins and numbers of aerosol particles. Studies encompassing the analyses of >100 size distributions of important intrinsic tracers of primary particles from HTC sources collected over the past decade in various environments show that urban aerosol contains a complex mixture of physically-discrete fresh and aged, primary particle populations from a variety of sources. Furthermore, whereas the behavior of fine-particulate aerosol mass and sulfate was described in terms of coagulation and accumulation aerosol scavenging of new secondary sulfate nuclei, studies reviewed herein suggest that the behavior of primary aerosol is mediated more by hygroscopic growth and cloud processing, accompanied by oxidation of SO{sub 2} on wet particles and droplets. The authors conclude that the distribution of airborne particulate toxins and their atmospheric behavior is far more complex than commonly conceptualized on the basis of the classical trimodal model, and they develop an extended paradigm in which the focus is on the primary accumulation aerosol.

Ondov, J.M. [Univ. of Maryland, College Park, MD (United States). Dept. of Chemistry and Biochemistry] [Univ. of Maryland, College Park, MD (United States). Dept. of Chemistry and Biochemistry; Wexler, A.S. [Univ. of Delaware, Newark, DE (United States). Dept. of Mechanical Engineering] [Univ. of Delaware, Newark, DE (United States). Dept. of Mechanical Engineering

1998-09-01T23:59:59.000Z

251

Ganges Valley Aerosol Experiment: Science and Operations Plan  

SciTech Connect (OSTI)

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 912 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 612 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 abundancein 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.

Kotamarthi, VR

2010-06-21T23:59:59.000Z

252

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

E-Print Network [OSTI]

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 ...

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.

2008-03-01T23:59:59.000Z

253

hal-00205429,version1-16Jan2008 On the number of droplets in aerosols  

E-Print Network [OSTI]

and pollution. Epidemics, radioactive elements can be carried by small droplets; volcanoes generate sulphated aerosols contributing to the destruction of the ozone layer. The planetary atmospheres are charged with such mixtures in suspension. The interaction between oceans and atmosphere generates mixtures of gas and water

Paris-Sud XI, Université de

254

Influence of the thermophoresis on aerosol deposition on warm urban surfaces P. Roupsard1  

E-Print Network [OSTI]

.roupsard@irsn.fr In the case of an accidental or chronic atmospheric pollution by a nuclear plant, aerosols' deposition in the radioactive plume on urban areas with the smallest uncertainties. In this case, deposition must be determined locally in urban canopy. In dry atmospheric conditions, transfer coefficients are defined by the dry

Paris-Sud XI, Université de

255

Characteristics of aerosol optical properties in pollution and Asian dust episodes  

E-Print Network [OSTI]

Characteristics of aerosol optical properties in pollution and Asian dust episodes over Beijing, China Chenbo Xie,1,2 Tomoki Nishizawa,2, * Nobuo Sugimoto,2 Ichiro Matsui,2 and Zifa Wang3 1 Atmospheric for Atmospheric Optics, Anhui Institute of Optics and Fine Mechanics, Chinese Academy of Sciences, Hefei, Anhui

256

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.

257

Aerosols and Clouds: In Cahoots to Change Climate  

SciTech Connect (OSTI)

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."

Berg, Larry

2014-03-29T23:59:59.000Z

258

Aerosols and Clouds: In Cahoots to Change Climate  

ScienceCinema (OSTI)

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."

Berg, Larry

2014-06-02T23:59:59.000Z

259

Parameterizations of Cloud Microphysics and Indirect Aerosol Effects  

SciTech Connect (OSTI)

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

Tao, Wei-Kuo [NASA/GSFC] [NASA/GSFC

2014-05-19T23:59:59.000Z

260

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

SciTech Connect (OSTI)

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.

Riihimaki, Laura; Shippert, Timothy

2014-11-05T23:59:59.000Z

Note: This page contains sample records for the topic "aerosols atmospheric profiling" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


261

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

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

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.

Riihimaki, Laura; Shippert, Timothy

262

Interactive Visualization of Modeled Atmospheric Trace Constituents Carmen M. Benkovitz  

E-Print Network [OSTI]

the effects of the emissions of Popocatepetl volcano, located near Mexico City. The effects of stronger of the Brookhaven National Laboratory Chemical Transport Model (CTM) of sulfate in the atmosphere. The visualization on climate. Anthropogenic activities affect the aerosol content of the atmosphere. Anthropogenic emissions

263

Experimental study of nuclear workplace aerosol samplers  

E-Print Network [OSTI]

LITERATURE REVIEW Aerosol Losses in an Inlet . Aerosol Losses in a Transport System Aerosol Losses in CAMs Critical Flow Venturi 8 13 15 16 EXPERIMENT PROCEDURE 18 CAM Evaluation Consideration FAS Evaluation Consideration Test Protocol Mixing... Chamber Setup High Speed Aerosol Wind Tunnel Setup Low Speed Aerosol Wind Tunnel Setup Critical Flow Venturi 18 19 21 22 24 25 27 RESULTS AND DISCUSSION Page 28 Aerosol Penetration through Transport Systems and CAM Areal Uniformity Deposits...

Parulian, Antony

2012-06-07T23:59:59.000Z

264

Secondary Aerosol: Precursors and Formation Mechanisms. Technical Report on Grant  

SciTech Connect (OSTI)

This project focused on studying trace gases that participate in chemical reactions that form atmospheric aerosols. Ammonium sulfate is a major constituent of these tiny particles, and one important pathway to sulfate formation is oxidation of dissolved sulfur dioxide by hydrogen peroxide in cloud, fog and rainwater. Sulfate aerosols influence the number and size of cloud droplets, and since these factors determine cloud radiative properties, sulfate aerosols also influence climate. Peroxide measurements, in conjunction with those of other gaseous species, can used to distinguish the contribution of in-cloud reaction to new sulfate aerosol formation from gas-phase nucleation reactions. This will lead to more reliable global climate models. We constructed and tested a new 4-channel fluorescence detector for airborne detection of peroxides. We integrated the instrument on the G-1 in January, 2006 and took a test flight in anticipation of the MAX-Mex field program, where we planned to fly under pressurized conditions for the first time. We participated in the 2006 Megacity Initiative: Local and Global Research Observations (MILAGRO) - Megacity Aerosol EXperiment ?? Mexico City (MAX-Mex) field measurement campaign. Peroxide instrumentation was deployed on the DOE G-1 research aircraft based in Veracruz, and at the surface site at Tecamac University.

Weinstein-Lloyd, Judith B

2009-05-04T23:59:59.000Z

265

Molecular Characterization of Biomass Burning Aerosols Using...  

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

Biomass Burning Aerosols Using High Resolution Mass Spectrometry. Molecular Characterization of Biomass Burning Aerosols Using High Resolution Mass Spectrometry. Abstract: Chemical...

266

The impact of biogenic carbon emissions on aerosol absorption inMexico City  

SciTech Connect (OSTI)

In order to determine the wavelength dependence of atmospheric aerosol absorption in the Mexico City area, the absorption angstrom exponents (AAEs) were calculated from aerosol absorption measurements at seven wavelengths obtained with a seven-channel aethalometer during two field campaigns, the Mexico City Metropolitan Area study in April 2003 (MCMA 2003) and the Megacity Initiative: Local and Global Research Observations in March 2006 (MILAGRO). The AAEs varied from 0.76 to 1.56 in 2003 and from 0.54 to 1.52 in 2006. The AAE values determined in the afternoon were consistently higher than the corresponding morning values, suggesting the photochemical formation of absorbing secondary organic aerosols (SOA) in the afternoon. The AAE values were compared to stable and radiocarbon isotopic measurements of aerosol samples collected at the same time to determine the sources of the aerosol carbon. The fraction of modern carbon (fM) in the aerosol samples, as determined from {sup 14}C analysis, showed that 70% of the carbonaceous aerosols in Mexico City were from modern sources, indicating a significant impact from biomass burning during both field campaigns. The {sup 13}C/{sup 12}C ratios of the aerosol samples illustrate the significant impact of Yucatan forest fires (C-3 plants) in 2003 and local grass fires (C-4 plants) at site T1 in 2006. A direct comparison of the fM values, stable carbon isotope ratios, and calculated aerosol AAEs suggested that the wavelength dependence of the aerosol absorption was controlled by the biogenically derived aerosol components.

Marley, N; Gaffney, J; Tackett, M J; Sturchio, N; Hearty, L; Martinez, N; Hardy, K D; Machany-Rivera, A; Guilderson, T P; MacMillan, A; Steelman, K

2009-02-24T23:59:59.000Z

267

THE DOE ATMOSPHERIC SCIENCE PROGRAM Highlights from the 2008 Science Team Meeting  

E-Print Network [OSTI]

atmospheric CO2 that would result in a given increase in global mean surface temperature. · Uncertainty Aerosol Experiment­MEXico City (MAX-MEX) ­ 2006. Cumulus Humilis Aerosol Processing Study (CHAPS) ­ OK in global chemical transport models and global climate models. Summary. DOE workshop on "grand challenges

Schwartz, Stephen E.

268

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelaware Electricity ProfileMichigan Electricity Profile

269

6, 75197562, 2006 Simulating aerosol  

E-Print Network [OSTI]

, particle number concentration and aerosol size-distribution. The model takes into account sulfate (SO4. This model system enables explicit simulations of the particle number concentration and size-distribution of aerosol dynamical processes (nucleation, condensation, coagulation) is evaluated by comparison

Paris-Sud XI, Université de

270

Alveolar targeting of aerosol pentamidine. Toward a rational delivery system  

SciTech Connect (OSTI)

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.

Simonds, A.K.; Newman, S.P.; Johnson, M.A.; Talaee, N.; Lee, C.A.; Clarke, S.W. (Royal Free Hospital, London (England))

1990-04-01T23:59:59.000Z

271

Temporal Variability of Aerosol Properties during TCAP: Impact on Radiative Forcing  

SciTech Connect (OSTI)

Ground-based remote sensing and in situ observations of aerosol microphysical and optical properties have been collected during summertime (June-August, 2012) as part of the Two-Column Aerosol Project (TCAP; http://campaign.arm.gov/tcap/), which was supported by the U.S. Department of Energys (DOEs) Atmospheric Radiation Measurement (ARM) Program (http://www.arm.gov/). The overall goal of the TCAP field campaign is to study the evolution of optical and microphysical properties of atmospheric aerosol transported from North America to the Atlantic and their impact on the radiation energy budget. During TCAP, the ground-based ARM Mobile Facility (AMF) was deployed on Cape Cod, an arm-shaped peninsula situated on the easternmost portion of Massachusetts (along the east coast of the United States) and that is generally downwind of large metropolitan areas. The AMF site was equipped with numerous instruments for sampling aerosol, cloud and radiative properties, including a Multi-Filter Rotating Shadowband Radiometer (MFRSR), a Scanning Mobility Particle Sizer (SMPS), an Aerodynamic Particle Sizer (APS), and a three-wavelength nephelometer. In this study we present an analysis of diurnal and day-to-day variability of the column and near-surface aerosol properties obtained from remote sensing (MFRSR data) and ground-based in situ measurements (SMPS, APS, and nephelometer data). In particular, we show that the observed diurnal variability of the MFRSR aerosol optical depth is strong and comparable with that obtained previously from the AERONET climatology in Mexico City, which has a larger aerosol loading. Moreover, we illustrate how the variability of aerosol properties impacts the direct aerosol radiative forcing at different time scales.

Kassianov, Evgueni I.; Barnard, James C.; Pekour, Mikhail S.; Berg, Larry K.; Fast, Jerome D.; Michalsky, Joseph J.; Lantz, K.; Hodges, G. B.

2013-11-01T23:59:59.000Z

272

156 | Triennial Scientific Report ADAGUC Atmospheric Data Access for the Geospatial User Community  

E-Print Network [OSTI]

Advanced Very High Resolution Radiometer BBC British Broadcasting Company BJEPB Beijing Environmental Radiometer AOGCM Atmosphere-Ocean General Circulation Model AOT Aerosol Optical Thickness API Application Potential Energy CERC Cambridge Environmental Research Consultants CESAR Cabauw Experimental Site

Stoffelen, Ad

273

ARM - Publications: Science Team Meeting Documents: Effects of Aerosol Size  

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth (AOD) by Microtops AtmosphericApplication andAn AssessmentARMArctic FacilityRetrievalsAerosol

274

ARM - Field Campaign - Two-Column Aerosol Project (TCAP)  

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth (AOD) by Microtops Atmospheric Optical DepthgovCampaignsSpring(PROBE)govCampaignsTwo-Column Aerosol

275

Regional variation of organic functional groups in aerosol particles on four U.S. east coast platforms during the International Consortium for  

E-Print Network [OSTI]

and secondary organic aerosol (SOA) formation. SOA can be formed by condensation of species produced by gas aerosol samples were collected during the International Consortium for Atmospheric Research on Transport) spectroscopy at all four sampling platforms. The ratio of molar concentrations of carbonyl C=O to saturated

276

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

SciTech Connect (OSTI)

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

Menon, Surabi; Del Genio, Anthony D.

2007-09-03T23:59:59.000Z

277

The Nearby Supernova Factory Ozone + Aerosol + Rayleigh  

E-Print Network [OSTI]

Rayleigh + Aerosol Extinction monitor filter Auxiliary Camera CCD Spectrograph picko ff mirror Umbra

278

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

SciTech Connect (OSTI)

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.

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

2014-11-27T23:59:59.000Z

279

aerosol particles collected: Topics by E-print Network  

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

Saller 2002-05-07 6 Nanomaterials from Aerosols Aerosols are suspensions of liquid or solid particles in a gas. Aerosol particles Materials Science Websites Summary: being clouds...

280

Mexico City Aerosol Analysis during MILAGRO using High Resolution...  

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

2: Mexico City Aerosol Analysis during MILAGRO using High Resolution Aerosol Mass Spectrometry at the Urban Supersite (T0). Part 2: Abstract: Submicron aerosol was analyzed during...

Note: This page contains sample records for the topic "aerosols atmospheric profiling" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


281

Mexico City Aerosol Analysis during MILAGRO using High Resolution...  

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

1: Mexico City Aerosol Analysis during MILAGRO using High Resolution Aerosol Mass Spectrometry at the Urban Supersite (T0). Part 1: Abstract: Submicron aerosol was analyzed during...

282

Cloud Condensation Nuclei Profile Value-Added Product  

SciTech Connect (OSTI)

The cloud condensation nuclei (CCN) concentration at cloud base is the most relevant measure of the aerosol that influences droplet formation in clouds. Since the CCN concentration depends on supersaturation, a more general measure of the CCN concentration is the CCN spectrum (values at multiple supersaturations). The CCN spectrum is now measured at the surface at several fixed ARM sites and by the ARM Mobile Facility (AMF), but is not measured at the cloud base. Rather than rely on expensive aircraft measurements for all studies of aerosol effects on clouds, a way to project CCN measurements at the surface to cloud base is needed. Remote sensing of aerosol extinction provides information about the vertical profile of the aerosol, but cannot be directly related to the CCN concentration because the aerosol extinction is strongly influenced by humidification, particularly near cloud base. Ghan and Collins (2004) and Ghan et al. (2006) propose a method to remove the influence of humidification from the extinction profiles and tie the dry extinction retrieval to the surface CCN concentration, thus estimating the CCN profile. This methodology has been implemented as the CCN Profile (CCNPROF) value-added product (VAP).

McFarlane, S; Sivaraman, C; Ghan, S

2012-10-08T23:59:59.000Z

283

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

SciTech Connect (OSTI)

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 (1020 km) until 510 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).

Koch, D

2011-03-20T23:59:59.000Z

284

CARES Helps Explain Secondary Organic Aerosols  

SciTech Connect (OSTI)

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.

Zaveri, Rahul

2014-03-28T23:59:59.000Z

285

CARES Helps Explain Secondary Organic Aerosols  

ScienceCinema (OSTI)

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.

Zaveri, Rahul

2014-06-02T23:59:59.000Z

286

Atmospheric Neutrinos  

E-Print Network [OSTI]

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.

Thomas K. Gaisser

2006-12-11T23:59:59.000Z

287

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]

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 ...

Guenther, A. B.

288

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

E-Print Network [OSTI]

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 ...

de Foy, B.

289

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

SciTech Connect (OSTI)

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.

Glenn C. England

2004-10-20T23:59:59.000Z

290

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

291

2010 Atmospheric System Research (ASR) Science Team Meeting Summary  

SciTech Connect (OSTI)

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.

Dupont, DL

2011-05-04T23:59:59.000Z

292

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

SciTech Connect (OSTI)

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.

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

2011-12-02T23:59:59.000Z

293

Microphysical Effects Determine Macrophysical Response for Aerosol Impacts on Deep Convective Clouds  

SciTech Connect (OSTI)

Deep convective clouds (DCCs) play a crucial role in the general circulation and energy and hydrological cycle of our climate system. Anthropogenic and natural aerosol particles can influence DCCs through changes in cloud properties, precipitation regimes, and radiation balance. Modeling studies have reported both invigoration and suppression of DCCs by aerosols, but none has fully quantified aerosol impacts on convection life cycle and radiative forcing. By conducting multiple month-long cloud-resolving simulations with spectral-bin cloud microphysics that capture the observed macro- and micro-physical properties of summer convective clouds in the tropics and mid-latitudes, this study provides the first comprehensive look at how aerosols affect cloud cover, cloud top height (CTH), and radiative forcing. Observations validate these simulation results. We find that microphysical aerosol effects contribute predominantly to increased cloud cover and CTH by inducing larger amount of smaller but longer lasting ice particles in the stratiform/anvils of DCCs with dynamical aerosol effects contributing at most ~ 1/4 of the total increase of cloud cover. The overall effect is a radiative warming in the atmosphere (3 to 5 W m-2) with strong surface cooling (-5 to -8 W m-2). Herein we clearly identified mechanisms more important than and additional to the invigoration effects hypothesized previously that explain the consistent signatures of increased cloud tops area and height by aerosols in DCCs revealed by observations.

Fan, Jiwen; Leung, Lai-Yung R.; Rosenfeld, Daniel; Chen, Qian; Li, Zhanqing; Zhang, Jinqiang; Yan, Hongru

2013-11-26T23:59:59.000Z

294

atmospheric infrared sounder: Topics by E-print Network  

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

Infrared Atmospheric Sounding Interferometer (IASI)Advanced Very High Resolution Radiometer (AVHRR Li, Jun 4 Ozone Profile Retrieval from an Advanced Infrared Sounder:...

295

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

SciTech Connect (OSTI)

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.

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

2013-09-01T23:59:59.000Z

296

Atmospheric processing of organic aerosols G. Barney Ellison  

E-Print Network [OSTI]

of an aqueous core that is encapsulated in an inert, hydrophobic organic monolayer. The organic materials important roles in climate and elsewhere through their interaction with solar and terrestrial radiation

Ellison, Barney

297

Atmospheric Aerosol Chemistry, Climate Change, and Air Quality  

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May JunDatastreamsmmcrcalgovInstrumentsruc DocumentationP-Series to someone byDear Friend,Arthur J. Nozik -GrownAn overhead viewAt-HomeR607

298

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May JunDatastreamsmmcrcalgovInstrumentsrucLas ConchasPassiveSubmittedStatus TomAboutManusScience and HowInsiderPrinceton Plasma Physics

299

ATMOSPHERIC AEROSOL RESEARCH ANNUAL REPORT 1975-76  

E-Print Network [OSTI]

of a) soot particles from propane-benzene combustion in air;tempera downstream from a propane Photoelectron spectraand carbon (Is) regions of propane soot particles produced

Novakov, T.

2010-01-01T23:59:59.000Z

300

High-resolution mass spectrometric analysis of secondary organic aerosol produced by ozonation of limonenew  

E-Print Network [OSTI]

and measured reaction products in the monomer product range. Introduction Atmospheric aerosols impact local air of both monomeric (m/z o 300) and oligomeric (m/z 4 300) condensed products of oxidation. A combination by previous studies. The isomerization reactions yield numerous products with a progressively increasing

Nizkorodov, Sergey

Note: This page contains sample records for the topic "aerosols atmospheric profiling" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


301

Supplement for "Secondary organic aerosol1 formation from idling gasoline passenger vehicle2  

E-Print Network [OSTI]

Supplement for "Secondary organic aerosol1 formation from idling gasoline passenger vehicle2.O. Box 503, FIN-00101 Helsinki, Finland}14 [5]{Department of Chemistry, Atmospheric Science, University experiment show a total concentration of light aromatics of less than 1 ppb.6 Vehicles7 In total six gasoline

Meskhidze, Nicholas

302

CHARACTERIZING THE INFLUENCE OF ANTHROPOGENIC EMISSIONS AND TRANSPORT VARIABILITY ON SULFATE AEROSOL CONCENTRATIONS AT MAUNA  

E-Print Network [OSTI]

CONCENTRATIONS AT MAUNA LOA OBSERVATORY Sulfate aerosol in the atmosphere has substantial impacts on human health confirmed that anthropogenic pollutants from Asian sources can be transported long distances with important implications for future air quality and global climate change. Located in the remote Pacific Ocean (19.54°N

Pierce, Jeffrey

303

Influence of anthropogenic aerosol on cloud optical depth and albedo shown by satellite measurements  

E-Print Network [OSTI]

- flux of sulfate aerosol from industrial regions of Europe or North America to remote areas of the North- atmosphere system over the industrial period and a cooling influence on climate. Estimates of the global), the negative sign indicating a cooling influence. Such a global mean forcing would more than offset the warming

304

Hygroscopic growth of submicron and supermicron aerosols in the marine boundary layer  

E-Print Network [OSTI]

balance and climate directly through absorption and scattering of the incoming solar radiation and indirectly through modification of cloud properties [Intergovernmental Panel on Climate Change, 2007 behaviors of the dynamic and complex atmospheric aerosol consisting of particles with a wide range of sizes

305

Significant aerosol direct radiative effects during a pollution episode in northern China  

E-Print Network [OSTI]

Significant aerosol direct radiative effects during a pollution episode in northern China J. Liu,1 during a heavy pollution episode that occurred in October 2004 over northern China are explored , resulting in solar heating of the atmosphere on the order of 300 Wm2 . Solar radiation reflected

Li, Zhanqing

306

Direct radiative forcing due to aerosols in Asia during Soon-Ung Parka,, Jaein I. Jeongb  

E-Print Network [OSTI]

Direct radiative forcing due to aerosols in Asia during March 2002 Soon-Ung Parka,, Jaein I. Jeongb Model (CRM) of Community Climate Model 3 and the output of the fifth generation of meso-scale model (MM5 in the global climate system by changing atmospheric radiation balance (Tegen and Fung, 1994; Andreae, 1996; Li

Park, Rokjin

307

Observations of new aerosol particle formation in a tropical urban Raghu Betha a  

E-Print Network [OSTI]

-19, Singapore 117576, Singapore b School of Earth and Environment, University of Leeds, Leeds LS2 9JT, United. These nucleation events were frequently observed during the SW monsoon period, but were rarely seen during the NE events were suppressed. ? 2013 Elsevier Ltd. All rights reserved. 1. Introduction Atmospheric aerosols

Spracklen, Dominick

308

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

SciTech Connect (OSTI)

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.

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

2011-11-23T23:59:59.000Z

309

Direct and semi-direct aerosol effects of Southern African1 biomass burning aerosol2  

E-Print Network [OSTI]

1 Direct and semi-direct aerosol effects of Southern African1 biomass burning aerosol2 Naoko effects of biomass burning aerosols from Southern African fires9 during July-October are investigated region the overall TOA radiative effect from the23 biomass burning aerosols is almost zero due

Wood, Robert

310

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

SciTech Connect (OSTI)

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.

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

2012-07-25T23:59:59.000Z

311

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May JunDatastreamsmmcrcalgovInstrumentsrucLasDelivered‰PNGExperience4AJ01)3,CloudgovCampaignsIR Cloud Camera Feasibility Study

312

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

SciTech Connect (OSTI)

The Importance of Clouds and Radiation for Climate Change: The Earths 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 Earths 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.

LR Roeder

2008-12-01T23:59:59.000Z

313

6, 93519388, 2006 Aerosol-cloud  

E-Print Network [OSTI]

ACPD 6, 9351­9388, 2006 Aerosol-cloud interaction inferred from MODIS and models G. Myhre et al Chemistry and Physics Discussions Aerosol-cloud interaction inferred from MODIS satellite data and global 6, 9351­9388, 2006 Aerosol-cloud interaction inferred from MODIS and models G. Myhre et al. Title

Paris-Sud XI, Université de

314

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelaware Electricity Profile 2012 Table 1. 2012 Summary

315

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelaware Electricity Profile 2012 Table 1. 2012

316

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelaware Electricity Profile 2012 Table 1. 2012Florida

317

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelaware Electricity Profile 2012 Table 1.

318

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelaware Electricity Profile 2012 Table 1.Hawaii

319

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelaware Electricity Profile 2012 Table 1.HawaiiIdaho

320

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelaware Electricity Profile 2012 Table

Note: This page contains sample records for the topic "aerosols atmospheric profiling" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


321

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelaware Electricity Profile 2012 TableIndiana

322

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelaware Electricity Profile 2012 TableIndianaIowa

323

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelaware Electricity Profile 2012 TableIndianaIowaKansas

324

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelaware Electricity Profile 2012

325

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelaware Electricity Profile 2012Louisiana Electricity

326

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelaware Electricity Profile 2012Louisiana

327

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelaware Electricity Profile 2012LouisianaMaryland

328

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelaware Electricity Profile

329

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelaware Electricity ProfileMichigan Electricity

330

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelaware Electricity ProfileMichigan

331

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelaware Electricity ProfileMichiganMissouri Electricity

332

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelaware Electricity ProfileMichiganMissouri

333

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelaware Electricity ProfileMichiganMissouriNebraska

334

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelaware ElectricityHampshire Electricity Profile 2012

335

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelaware ElectricityHampshire Electricity Profile

336

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelaware ElectricityHampshire Electricity ProfileMexico

337

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelawareTexas Electricity Profile 2012 Table 1. 2012

338

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelawareTexas Electricity Profile 2012 Table 1.

339

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelawareTexas Electricity Profile 2012 Table 1.Utah

340

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelawareTexas Electricity Profile 2012 Table

Note: This page contains sample records for the topic "aerosols atmospheric profiling" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


341

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelawareTexas Electricity Profile 2012 TableVirginia

342

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelawareTexas Electricity Profile 2012

343

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelawareTexas Electricity Profile 2012West Virginia

344

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelawareTexas Electricity Profile 2012West

345

EIA - State Electricity 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelawareTexas Electricity Profile 2012WestWyoming

346

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelawareTexas Electricity Profile 2012WestWyomingAlabama

347

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelawareTexas Electricity Profile

348

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelawareTexas Electricity ProfileArkansas Nuclear

349

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelawareTexas Electricity ProfileArkansas

350

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelawareTexas Electricity ProfileArkansasConnecticut

351

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelawareTexas ElectricityGeorgia Nuclear Profile 2010

352

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelawareTexas ElectricityGeorgia Nuclear Profile

353

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelawareTexas ElectricityGeorgia Nuclear ProfileIowa

354

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelawareTexasMissouri Nuclear Profile 2010 Missouri

355

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelawareTexasMissouri Nuclear Profile 2010

356

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelawareTexasMissouri Nuclear Profile 2010Hampshire

357

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelawareTexasMissouri Nuclear Profile

358

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelawareTexasMissouri Nuclear ProfileYork Nuclear

359

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelawareTexasMissouri Nuclear ProfileYork NuclearNorth

360

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelawareTexasMissouri Nuclear ProfileYork

Note: This page contains sample records for the topic "aerosols atmospheric profiling" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


361

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelawareTexasMissouri Nuclear ProfileYorkPennsylvania

362

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelawareTexasMissouri NuclearTennessee profile Tennessee

363

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelawareTexasMissouri NuclearTennessee profile

364

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelawareTexasMissouri NuclearTennessee profileVermont

365

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutron scatteringDelawareTexasMissouri NuclearTennesseeWashington profile

366

Effects of Aerosols on Autumn Precipitation over Mid-Eastern China  

SciTech Connect (OSTI)

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.

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

2014-09-20T23:59:59.000Z

367

Influence of sky radiance measurement errors on inversion-retrieved aerosol properties  

SciTech Connect (OSTI)

Remote sensing of the atmospheric aerosol is a well-established technique that is currently used for routine monitoring of this atmospheric component, both from ground-based and satellite. The AERONET program, initiated in the 90's, is the most extended network and the data provided are currently used by a wide community of users for aerosol characterization, satellite and model validation and synergetic use with other instrumentation (lidar, in-situ, etc.). Aerosol properties are derived within the network from measurements made by ground-based Sun-sky scanning radiometers. Sky radiances are acquired in two geometries: almucantar and principal plane. Discrepancies in the products obtained following both geometries have been observed and the main aim of this work is to determine if they could be justified by measurement errors. Three systematic errors have been analyzed in order to quantify the effects on the inversion-derived aerosol properties: calibration, pointing accuracy and finite field of view. Simulations have shown that typical uncertainty in the analyzed quantities (5% in calibration, 0.2 Degree-Sign in pointing and 1.2 Degree-Sign field of view) yields to errors in the retrieved parameters that vary depending on the aerosol type and geometry. While calibration and pointing errors have relevant impact on the products, the finite field of view does not produce notable differences.

Torres, B.; Toledano, C.; Cachorro, V. E.; Bennouna, Y. S.; Fuertes, D.; Gonzalez, R.; Frutos, A. M. de [Atmospheric Optics Group (GOA), University of Valladolid, Valladolid (Spain); Berjon, A. J. [Izana Atmospheric Research Center, Meteorological State Agency of Spain (AEMET), Sta. Cruz de Tenerife (Spain); Dubovik, O.; Goloub, P.; Podvin, T.; Blarel, L. [Laboratory of Atmospheric Optics, Universite Lille 1, Villeneuve d'Ascq (France)

2013-05-10T23:59:59.000Z

368

Investigation of Aerosol Indirect Effects using a Cumulus Microphysics Parameterization in a Regional Climate Model  

SciTech Connect (OSTI)

A new Zhang and McFarlane (ZM) cumulus scheme includes a two-moment cloud microphysics parameterization for convective clouds. This allows aerosol effects to be investigated more comprehensively by linking aerosols with microphysical processes in both stratiform clouds that are explicitly resolved and convective clouds that are parameterized in climate models. This new scheme is implemented in the Weather Research and Forecasting (WRF) model, which is coupled with the physics and aerosol packages from the Community Atmospheric Model version 5 (CAM5). A test case of July 2008 during the East Asian summer monsoon is selected to evaluate the performance of the new ZM scheme and to investigate aerosol effects on monsoon precipitation. The precipitation and radiative fluxes simulated by the new ZM scheme show a better agreement with observations compared to simulations with the original ZM scheme that does not include convective cloud microphysics and aerosol convective cloud interactions. Detailed analysis suggests that an increase in detrained cloud water and ice mass by the new ZM scheme is responsible for this improvement. To investigate precipitation response to increased anthropogenic aerosols, a sensitivity experiment is performed that mimics a clean environment by reducing the primary aerosols and anthropogenic emissions to 30% of that used in the control simulation of a polluted environment. The simulated surface precipitation is reduced by 9.8% from clean to polluted environment and the reduction is less significant when microphysics processes are excluded from the cumulus clouds. Ensemble experiments with ten members under each condition (i.e., clean and polluted) indicate similar response of the monsoon precipitation to increasing aerosols.

Lim, Kyo-Sun; Fan, Jiwen; Leung, Lai-Yung R.; Ma, Po-Lun; Singh, Balwinder; Zhao, Chun; Zhang, Yang; Zhang, Guang; Song, Xiaoliang

2014-01-29T23:59:59.000Z

369

Atmospheric Environment ] (  

E-Print Network [OSTI]

and the other site was located downwind of the city to study the effect of the urban area on the stability energy budget located throughout Oklahoma City. Three wind-profiling radars were used to measure wind mixing heights during the Joint URBAN (2003) experiment in Oklahoma City, Oklahoma. AERMET is a simple 2

Raman, Sethu

370

Direct Aerosol Forcing: Sensitivity to Uncertainty in Measurements of  

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed Newcatalyst phasesData FilesShape,PhysicsDileepDirac Charge DynamcsAerosol

371

Importance of Iron Mineralogy to Aerosol Solubility: Potential Effects of  

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation ProposedUsingFun withconfinementEtching. |EndecahemeEMSLImagingOregonAerosol Source on

372

Aerosol Simulations by LLNL IMPACT and Comparisons with Field Measurements  

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth (AOD)ProductssondeadjustsondeadjustAbout the BuildingInnovation 2011 Simulation StudiesAerosol Remote

373

Ganges Valley Aerosol 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation ProposedUsingFun with Big Sky Learning Fun with Big SkyDIII-DRMRGamma Radiation and

374

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth (AOD)ProductssondeadjustsondeadjustAbout the BuildingInnovation 2011 Simulation Studies ofBusiness Forum2

375

Review of models applicable to accident aerosols  

SciTech Connect (OSTI)

Estimations of potential airborne-particle releases are essential in safety assessments of nuclear-fuel facilities. This report is a review of aerosol behavior models that have potential applications for predicting aerosol characteristics in compartments containing accident-generated aerosol sources. Such characterization of the accident-generated aerosols is a necessary step toward estimating their eventual release in any accident scenario. Existing aerosol models can predict the size distribution, concentration, and composition of aerosols as they are acted on by ventilation, diffusion, gravity, coagulation, and other phenomena. Models developed in the fields of fluid mechanics, indoor air pollution, and nuclear-reactor accidents are reviewed with this nuclear fuel facility application in mind. The various capabilities of modeling aerosol behavior are tabulated and discussed, and recommendations are made for applying the models to problems of differing complexity.

Glissmeyer, J.A.

1983-07-01T23:59:59.000Z

376

Development of Aerosol Models for Radiative Flux Calculations at ARM Sites: Utility of Trajectory Clustering for Characterizing Aerosol Climatology  

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed Newcatalyst phasesData FilesShape, Density,TiO2(110).Development of Aerosol Models

377

Large historical changes of fossil-fuel black carbon aerosols  

SciTech Connect (OSTI)

Anthropogenic emissions of fine black carbon (BC) particles, the principal light-absorbing atmospheric aerosol, have varied during the past century in response to changes of fossil-fuel utilization, technology developments, and emission controls. We estimate historical trends of fossil-fuel BC emissions in six regions that represent about two-thirds of present day emissions and extrapolate these to global emissions from 1875 onward. Qualitative features in these trends show rapid increase in the latter part of the 1800s, the leveling off in the first half of the 1900s, and the re-acceleration in the past 50 years as China and India developed. We find that historical changes of fuel utilization have caused large temporal change in aerosol absorption, and thus substantial change of aerosol single scatter albedo in some regions, which suggests that BC may have contributed to global temperature changes in the past century. This implies that the BC history needs to be represented realistically in climate change assessments.

Novakov, T.; Ramanathan, V.; Hansen, J.E.; Kirchstetter, T.W.; Sato, M.; Sinton, J.E.; Sathaye, J.A.

2002-09-26T23:59:59.000Z

378

Stratospheric Aerosol Geoengineering ALAN ROBOCK  

E-Print Network [OSTI]

Stratospheric Aerosol Geoengineering ALAN ROBOCK ABSTRACT In response to global warming, one suggested geoengineering response involves creating a cloud of particles in the stratosphere to reflect some, the volcano analog also warns against geoengineering because of responses such as ozone depletion, regional

Robock, Alan

379

DO AEROSOLS CHANGE CLOUD COVER AND AFFECT CLIMATE?  

E-Print Network [OSTI]

BALANCE Global and annual average energy fluxes in watts per square meter Schwartz, 1996, modified from;AEROSOL INFLUENCES ON CLIMATE AND CLIMATE CHANGE #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

Schwartz, Stephen E.

380

The effects of emission of anthropogenic chemical species on chemical and physical properties of aerosols  

SciTech Connect (OSTI)

Numerical studies have been carried out to examine the effects of chemically reactive trace gases emitted into the atmosphere on the evolution of chemical species concentrations, on the chemical composition and size distribution of airborne particles, and on optical properties of aerosols. Argonne`s chemistry module has been modified by refining the treatment of gas-to-particle conversion. The changes in size distribution and chemical composition of aerosols are calculated with consideration of heteramolecular diffusion and coagulation. Results of the 24 h real-time simulation indicate that the maximum oxidation rate of sulfur dioxide is about 0.4% h{sup {minus}1}; that the total aerosol volume increases with the increase in relative humidity by as much as 36% (due mainly to the collection of sulfuric acid embryos by preexisting particles); and that the surface area, a measure of optical depth, increases with the increase in relative humidity by as much as 27%.

Lee, In Young

1994-07-01T23:59:59.000Z

Note: This page contains sample records for the topic "aerosols atmospheric profiling" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
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381

Modeling Activities in the Department of Energys Atmospheric Sciences Program  

SciTech Connect (OSTI)

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.

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

2009-03-01T23:59:59.000Z

382

Amine-Amine Exchange in Aminium-Methanesulfonate Aerosols  

SciTech Connect (OSTI)

Aerosol particles are ubiquitous in the atmosphere and have been shown to impact the Earths 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.

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

2014-12-18T23:59:59.000Z

383

Atmosphere Model  

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth (AOD)ProductssondeadjustsondeadjustAbout theOFFICEAmesApplication2ArgonneAssemblyDemandPlasma4 Medicare5Dust

384

Use of a continuous stirred tank reactor for the study of aqueous aerosol chemistry  

SciTech Connect (OSTI)

Atmospheric aerosol chemistry is important in areas ranging from urban air pollution to cloud formation. It has long been supposed that droplet-phase reactions account for a significant fraction of the atmospheric conversion of SO/sub 2/ to sulfate. In this thesis a reactor system is developed to carry out gas-aerosol reactions under humid, ambient-like conditions. The apparatus consists of a continuous stirred tank reactor (CSTR) in which the growth of the aqueous aerosol is measured. Absence of mass transfer limitation, coagulation, and nucleation ensure that particle growth is direct evidence of reaction. Special care is taken to minimize size biasing of the aqueous aerosol in the electrostatics classifier used to measure the reactor feed and effluent distributions. Aerosol behavior in the reactor is modeled assuming an ideal CSTR and, given the solution thermodynamics and equilibrium chemistry, the effluent distribution can be predicted using one of the proposed reaction rate mechanisms. Experiments were performed using a pure MnSO/sub 4/ or a MnSO/sub 4/minus// Na/sub 2/SO/sub 4/ mixture feed aerosol. The relative humidity ranged from 86 to 94% and 0.1 ppm < p/sub SO/sub 2// < 50 ppm. The various rate expressions proposed for this system in the literature resulted in varying estimates of growth. When reactor conditions were similar to those at which the rate expression was determined, the agreement between the predicted and observed distributions improved. This indicates that use of a rate expressions beyond its specified range may result in erroneous predictions.

Adkins, C.L.J.

1988-01-01T23:59:59.000Z

385

Water Structure at Aqueous Solution Surfaces of Atmospherically Relevant Dimethyl Sulfoxide and Methanesulfonic Acid Revealed by Phase-Sensitive Sum Frequency  

E-Print Network [OSTI]

layer (MBL), the sulfur cycle dominates in the gas-to-particle conversion process and in the growth-containing aerosols play an important role in atmospheric chemistry and climate.1-3 Especially in the marine boundary

386

Spectro-Microscopic Measurements of Carbonaceous Aerosol Aging in Central California  

SciTech Connect (OSTI)

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.

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

2013-10-29T23:59:59.000Z

387

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

SciTech Connect (OSTI)

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.

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.

2012-03-30T23:59:59.000Z

388

Optimization of aerosol penetration through transport lines  

E-Print Network [OSTI]

will be minimum and -' he penetration of aerosols through the transport system will be maximal. It is the purpose of the study reported herein to experimentally investigate the optimization of aerosol penetration through transport systems and to obtain a... numbers less than 869, bounded the use of this model to Reynolds numbers less than or equal to 1100. 19 IV. SUNNARY OF WORK AND EXPERINENTAL NETHODOLOGY The purpose of the study reported herein was to further analyze the optimization of aerosol...

Wong Luque, Fermin Samuel

1992-01-01T23:59:59.000Z

389

Direct and semidirect aerosol effects of southern African biomass burning aerosol  

E-Print Network [OSTI]

Direct and semidirect aerosol effects of southern African biomass burning aerosol Naoko Sakaeda,1 2011; published 21 June 2011. [1] Direct and semidirect radiative effects of biomass burning aerosols static stability. Over the entire region the overall TOA radiative effect from the biomass burning

Wood, Robert

390

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

SciTech Connect (OSTI)

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.

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

2013-06-11T23:59:59.000Z

391

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,...

392

Separating Cloud Forming Nuclei from Interstitial Aerosol  

SciTech Connect (OSTI)

It has become important to characterize the physicochemical properties of aerosol that have initiated the warm and ice clouds. The data is urgently needed to better represent the aerosol-cloud interaction mechanisms in the climate models. The laboratory and in-situ techniques to separate precisely the aerosol particles that act as cloud condensation nuclei (CCN) and ice nuclei (IN), termed as cloud nuclei (CN) henceforth, have become imperative in studying aerosol effects on clouds and the environment. This review summarizes these techniques, design considerations, associated artifacts and challenges, and briefly discusses the need for improved designs to expand the CN measurement database.

Kulkarni, Gourihar R.

2012-09-12T23:59:59.000Z

393

Indirect and Semi-Direct Aerosol Campaign  

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

October? 2. To what extent do the different properties of the Arctic aerosol during April produce differences in clouds? * Do the more polluted conditions during April in the...

394

An Aerosol Condensation Model for Sulfur Trioxide  

SciTech Connect (OSTI)

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

Grant, K E

2008-02-07T23:59:59.000Z

395

Experiment Profile:  

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation ProposedUsing ZirconiaPolicy and Assistance100 tonusingdeposition.EnergyExpedited6 DES and

396

People 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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary)morphinanInformation Desert Southwest RegionatSearch Welcome to the PacificCollaboration »People Profiles Featured

397

A Computational Approach to Understanding Aerosol Formation and Oxidant Chemistry in the Troposphere  

SciTech Connect (OSTI)

An understanding of the mechanisms and kinetics of aerosol formation and ozone production in the troposphere is currently a high priority because these phenomena are recognized as two major effects of energy-related air pollution. Atmospheric aerosols are of concern because of their effect on visibility, climate, and human health. Equally important, aerosols can change the chemistry of the atmosphere, in dramatic fashion, by providing new chemical pathways (in the condensed phase) unavailable in the gas phase. The oxidation of volatile organic compounds (VOCs) and inorganic compounds (e.g., sulfuric acid, ammonia, nitric acid, ions, and mineral) can produce precursor molecules that act as nucleation seeds. The U.S. Department of Energy (DOE) Atmospheric Chemistry Program (ACP) has identified the need to evaluate the causes of variations in tropospheric aerosol chemical composition and concentrations, including determining the sources of aerosol particles and the fraction of such that are of primary and secondary origin. In particular, the ACP has called for a deeper understanding into aerosol formation because nucleation creates substantial concentrations of fresh particles that, via growth and coagulation, influence the Earth's radiation budget. Tropospheric ozone is also of concern primarily because of its impact on human health. Ozone levels are controlled by NOx and by VOCs in the lower troposphere. The VOCs can be either from natural emissions from such sources as vegetation and phytoplankton or from anthropogenic sources such as automobiles and oil-fueled power production plants. The major oxidant for VOCs in the atmosphere is the OH radical. With the increase in VOC emissions, there is rising concern regarding the available abundance of HOx species needed to initiate oxidation. Over the last five years, there have been four field studies aimed at initial measurements of HOx species (OH and HO? radicals). These measurements revealed HOx levels that are two to four times higher than expected from the commonly assumed primary sources. Such elevated abundances of HOx imply a more photochemically active troposphere than previously thought. This implies that rates of ozone formation in the lower region of the atmosphere and the oxidation of SO? can be enhanced, thus promoting the formation of new aerosol properties. Central to unraveling this chemistry is the ability to assess the photochemical product distributions resulting from the photodissociation of by-products of VOC oxidation. We propose to use state-of-the-art theoretical techniques to develop a detailed understanding of the mechanisms of aerosol formation in multicomponent (mixed chemical) systems and the photochemistry of atmospheric organic species. The aerosol studies involve an approach that determines homogeneous gas-particle nucleation rates from knowledge of the molecular interactions that are used to define properties of molecular clusters. Over the past several years we developed Dynamical Nucleation Theory (DNT), a novel advance in the theoretical description of homogeneous gas-liquid nucleation, and applied it to gas-liquid nucleation of a single component system (e.g., water). The goal of the present research is to build upon these advances by extending the theory to multicomponent systems important in the atmosphere (such as clusters containing sulfuric acid, water, ions, ammonia, and organics). In addition, high-level ab initio electronic structure calculations will be used to unravel the chemical reactivity of the OH radical and water clusters.

Francisco, Joseph S.; Kathmann, Shawn M.; Schenter, Gregory K.; Dang, Liem X.; Xantheas, Sotiris S.; Garrett, Bruce C.; Du, Shiyu; Dixon, David A.; Bianco, Roberto; Wang, Shuzhi; Hynes, James T.; Morita, Akihiro; Peterson, Kirk A.

2006-04-18T23:59:59.000Z

398

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

SciTech Connect (OSTI)

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

Hu, Ning; Liu, Xiaohong

2013-10-01T23:59:59.000Z

399

An optimal fitting approach to improve the GISS ModelE aerosol optical property parameterization using AERONET data  

E-Print Network [OSTI]

and absorbing solar radiation and the indirect effect by interacting with water vapor to affect cloud formation and lifetime. Absorbing aerosols also have the semidirect effect by heating the atmosphere layer, reducing; Intergovernmental Panel on Climate Change, 2001]. [3] Globalscale models, which simulate the emission, transport

400

Reduction in biomass burning aerosol light absorption upon humidificat...  

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

in biomass burning aerosol light absorption upon humidification: Roles of inorganically-induced hygroscopicity, Reduction in biomass burning aerosol light absorption upon...

Note: This page contains sample records for the topic "aerosols atmospheric profiling" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


401

aerosols iii morphologic: Topics by E-print Network  

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

Sciences Websites Summary: of aerosols. Keywords: metal waste recycling; aerosols; fire hazard; explosion hazard. 1. OVERVIEW ProductsRisks generated by the treatment of...

402

ambient ultrafine aerosols: Topics by E-print Network  

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

soluble in water: 2. Isolation of acid, neutral, and basic fractions by modified size Weber, Rodney 4 Ambient aerosol sampling using the Aerodyne Aerosol Mass Spectrometer...

403

Synergy between Secondary Organic Aerosols and Long Range Transport...  

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

between Secondary Organic Aerosols and Long Range Transport of Polycyclic Aromatic Hydrocarbons. Synergy between Secondary Organic Aerosols and Long Range Transport of Polycyclic...

404

acid aerosol exposure: Topics by E-print Network  

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

Nenes, Athanasios 8 Neutralization of soil aerosol and its impact on the distribution of acid rain over east Asia Geosciences Websites Summary: Neutralization of soil aerosol and...

405

Aerosol Composition and Source Apportionment in the Mexico City...  

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

Aerosol Composition and Source Apportionment in the Mexico City Metropolitan Area with PIXEPESASTIM and Multivariate Analysis. Aerosol Composition and Source Apportionment in the...

406

Molecular Chemistry of Organic Aerosols Through the Application...  

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

Chemistry of Organic Aerosols Through the Application of High Resolution Mass Spectrometry. Molecular Chemistry of Organic Aerosols Through the Application of High Resolution Mass...

407

aerosol samples collected: Topics by E-print Network  

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

elements analysis of aerosol samples from some CiteSeer Summary: Aerosols deposits on filters from ten Romanian towns with different kinds and levels of industrial development...

408

Optical, physical, and chemical properties of springtime aerosol...  

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

Optical, physical, and chemical properties of springtime aerosol over Barrow Alaska in 2008. Optical, physical, and chemical properties of springtime aerosol over Barrow Alaska in...

409

aerosol particles emitted: Topics by E-print Network  

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

aerosols scatter and absorb solar, estimates of the impact of aerosols on visibility, the solar radiation balance, and crop production is presented. 1. INTRODUCTION The attenuation...

410

aerosolized pentamidine effect: Topics by E-print Network  

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

ON CCN CONCENTRATION AND AEROSOL FIRST INDIRECT RADIATIVE composition, aerosol size distribution is the more dominant parameter on CCN activation Feingold, GRL 2003;...

411

aerosols radioactifs artificiels: Topics by E-print Network  

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

ON CCN CONCENTRATION AND AEROSOL FIRST INDIRECT RADIATIVE composition, aerosol size distribution is the more dominant parameter on CCN activation Feingold, GRL 2003;...

412

aerosol particle analysis: Topics by E-print Network  

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

Summary: data analysis algorithm is presented. Our earlier algorithm assumed a monomodal aerosol size distribution, while the new algorithm allows us to partition the aerosol...

413

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...

414

The dependence of ice microphysics on aerosol concentration in...  

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

The dependence of ice microphysics on aerosol concentration in arctic mixed-phase stratus clouds during ISDAC and M-PACE. The dependence of ice microphysics on aerosol...

415

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.

416

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

SciTech Connect (OSTI)

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.

Zahn, S.G.

1993-12-01T23:59:59.000Z

417

Heterogeneous Chemistry: Understanding Aerosol/Oxidant Interactions  

SciTech Connect (OSTI)

Global radiative forcing of nitrate and ammonium aerosols has mostly been estimated from aerosol concentrations calculated at thermodynamic equilibrium or using approximate treatments for their uptake by aerosols. In this study, a more accurate hybrid dynamical approach (DYN) was used to simulate the uptake of nitrate and ammonium by aerosols and the interaction with tropospheric reactive nitrogen chemistry in a three-dimensional global aerosol and chemistry model, IMPACT, which also treats sulfate, sea salt and mineral dust aerosol. 43% of the global annual average nitrate aerosol burden, 0.16 TgN, and 92% of the global annual average ammonium aerosol burden, 0.29 TgN, exist in the fine mode (D<1.25 {micro}m) that scatters most efficiently. Results from an equilibrium calculation differ significantly from those of DYN since the fraction of fine-mode nitrate to total nitrate (gas plus aerosol) is 9.8%, compared to 13% in DYN. Our results suggest that the estimates of aerosol forcing from equilibrium concentrations will be underestimated. We also show that two common approaches used to treat nitrate and ammonium in aerosol in global models, including the first-order gas-to-particle approximation based on uptake coefficients (UPTAKE) and a hybrid method that combines the former with an equilibrium model (HYB), significantly overpredict the nitrate uptake by aerosols especially that by coarse particles, resulting in total nitrate aerosol burdens higher than that in DYN by +106% and +47%, respectively. Thus, nitrate aerosol in the coarse mode calculated by HYB is 0.18 Tg N, a factor of 2 more than that in DYN (0.086 Tg N). Excessive formation of the coarse-mode nitrate in HYB leads to near surface nitrate concentrations in the fine mode lower than that in DYN by up to 50% over continents. In addition, near-surface HNO{sub 3} and NO{sub x} concentrations are underpredicted by HYB by up to 90% and 5%, respectively. UPTAKE overpredicts the NO{sub x} burden by 56% and near-surface NO{sub x} concentrations by a factor of 2-5. These results suggest the importance of using the more accurate hybrid dynamical method in the estimates of both aerosol forcing and tropospheric ozone chemistry.

Joyce E. Penner

2005-03-14T23:59:59.000Z

418

NUCLEAR NON-PROLIFERATION-TASK 1: Deployable Plume and Aerosol Release Prediction and Tracking System  

SciTech Connect (OSTI)

This contract was awarded in response to a proposal in which a deployable plume and aerosol release prediction and tracking system would be designed, fabricated, and tested. The system would gather real time atmospheric data and input it into a real time atmospheric model that could be used for plume predition and tracking. The system would be able to be quickly deployed by aircraft to points of interest or positioned for deployment by vehicles. The system would provide three dimensional (u, v, and w) wind vector data, inversion height measurements, surface wind information, classical weather station data, and solar radiation. The on-board real time computer model would provide the prediction of the behavior of plumes and released aerosols.

John Kleppe, Ph.D., William Norris, Ph.D., Mehdi Etezada, Ph.D., P.E.

2006-07-19T23:59:59.000Z

419

Characterization of aerosols produced by surgical procedures  

SciTech Connect (OSTI)

In many surgeries, especially orthopedic procedures, power tools such as saws and drills are used. These tools may produce aerosolized blood and other biological material from bone and soft tissues. Surgical lasers and electrocautery tools can also produce aerosols when tissues are vaporized and condensed. Studies have been reported in the literature concerning production of aerosols during surgery, and some of these aerosols may contain infectious material. Garden et al. (1988) reported the presence of papilloma virus DNA in the fumes produced from laser surgery, but the infectivity of the aerosol was not assessed. Moon and Nininger (1989) measured the size distribution and production rate of emissions from laser surgery and found that particles were generally less than 0.5 {mu}m diameter. More recently there has been concern expressed over the production of aerosolized blood during surgical procedures that require power tools. In an in vitro study, the production of an aerosol containing the human immunodeficiency virus (HIV) was reported when power tools were used to cut tissues with blood infected with HIV. Another study measured the size distribution of blood aerosols produced by surgical power tools and found blood-containing particles in a number of size ranges. Health care workers are anxious and concerned about whether surgically produced aerosols are inspirable and can contain viable pathogens such as HIV. Other pathogens such as hepatitis B virus (HBV) are also of concern. The Occupational Safety and Health funded a project at the National Institute for Inhalation Toxicology Research Institute to assess the extent of aerosolization of blood and other tissues during surgical procedures. This document reports details of the experimental and sampling approach, methods, analyses, and results on potential production of blood-associated aerosols from surgical procedures in the laboratory and in the hospital surgical suite.

Yeh, H.C.; Muggenburg, B.A.; Lundgren, D.L.; Guilmette, R.A.; Snipes, M.B.; Jones, R.K. [Inhalation Toxicology Research Institute, Albuquerque, NM (United States); Turner, R.S. [Lovelace Health Systems, Albuquerque, NM (United States)

1994-07-01T23:59:59.000Z

420

Assessing temporal and spatial variations in atmospheric dust over Saudi Arabia through satellite, radiometric, and station data  

E-Print Network [OSTI]

1 Assessing temporal and spatial variations in atmospheric dust over Saudi Arabia through satellite Saud University, Riyadh, Saudi Arabia #12;2 Abstract1 Temporal and spatial variations in atmospheric dust over Saudi Arabia are studied for 2000-20102 using satellite and ground-based Aerosol Optical

Wisconsin at Madison, University of

Note: This page contains sample records for the topic "aerosols atmospheric profiling" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


421

Atmos. Chem. Phys., 3, 18871902, 2003 www.atmos-chem-phys.org/acp/3/1887/ Atmospheric  

E-Print Network [OSTI]

Atmos. Chem. Phys., 3, 1887­1902, 2003 www.atmos-chem-phys.org/acp/3/1887/ Atmospheric Chemistry, Germany 2Institute of Atmospheric Physic, DLR, Oberpfaffenhofen, D-82234 Wessling, Germany 3Max-platform field campaign to measure long-range transport of air-pollution and aerosols from South East Asia

Paris-Sud XI, Université de

422

Improving Bulk Microphysics Parameterizations in Simulations of Aerosol Effects  

SciTech Connect (OSTI)

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.

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

2013-06-05T23:59:59.000Z

423

Aircraft Observations of Sub-cloud Aerosol and Convective Cloud Physical Properties  

E-Print Network [OSTI]

of Department, Kenneth Bowman December 2009 Major Subject: Atmospheric Sciences iii iii ABSTRACT Aircraft Observations of Sub-Cloud Aerosol and Convective Cloud Physical Properties. (December 2009) Duncan Axisa, B.Ed., University of Malta; B... but for vertical velocity (ms-1). Negative values are updraft and positive values are downdraft ........................................... 30 18 Cloud droplet size distribution (dN/dlogD, cm-3) for 1Hz cloud penetration data...

Axisa, Duncan

2011-02-22T23:59:59.000Z

424

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

SciTech Connect (OSTI)

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.

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

2010-10-01T23:59:59.000Z

425

Indirect radiative forcing by ion-mediated nucleation of aerosol  

SciTech Connect (OSTI)

A clear understanding of particle formation mechanisms is critical for assessing aerosol indirect radiative forcing and associated climate feedback processes. Recent studies reveal the importance of ion-mediated nucleation (IMN) in generating new particles and cloud condensation nuclei (CCN) in the atmosphere. Here we implement for the first time a physically based treatment of IMN into the Community Atmosphere Model version 5. Our simulations show that, compared to globally averaged results based on binary homogeneous nucleation (BHN), the presence of ionization (i.e., IMN) halves H2SO4 column burden, but increases the column integrated nucleation rate by around one order of magnitude, total particle number burden by a factor of ~ 3, CCN burden by ~ 10% (at 0.2% supersaturation) to 65% (at 1.0% supersaturation), and cloud droplet number burden by ~ 18%. Compared to BHN, IMN increases cloud liquid water path by 7.5%, decreases precipitation by 1.1%, and increases total cloud cover by 1.9%. This leads to an increase of total shortwave cloud radiative forcing by 3.67 W/m2 (more negative) and longwave cloud forcing by 1.78 W/m2 (more positive), resulting in a -1.9 W/m2 net change in cloud radiative forcing associated with IMN. The significant impacts of ionization on global aerosol formation, CCN abundance, and cloud radiative forcing may provide an important physical mechanism linking the global energy balance to various processes affecting atmospheric ionization, which should be properly represented in climate models.

Yu, Fangqun; Luo, Gan; Liu, Xiaohong; Easter, Richard C.; Ma, Xiaoyan; Ghan, Steven J.

2012-12-03T23:59:59.000Z

426

Linearity of Climate Response to Increases in Black Carbon Aerosols  

SciTech Connect (OSTI)

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.

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

2013-01-01T23:59:59.000Z

427

ENCAPSULATION EFFECTS ON CARBONACEOUS AEROSOL LIGHT ABSORPTION  

E-Print Network [OSTI]

ENCAPSULATION EFFECTS ON CARBONACEOUS AEROSOL LIGHT ABSORPTION Arthur Sedlacek, Brookhaven National of aerosol absorption on direct radiative forcing is still an active area of research, in part, because. This poster presents data on black carbon (BC) light absorption measured by Photothermal Interferometry

428

2, 12871315, 2002 Aerosol sources and  

E-Print Network [OSTI]

in climate variability and climate change studies (IPCC, 2001). Radiative forcing of natural and their contribution to the chemical composition of aerosols in the Eastern Mediterranean Sea during summertime J aerosol sources in the Eastern Mediterranean5 Basin could be investigated at this location since the site

Paris-Sud XI, Université de

429

6, 1217912197, 2006 Aerosol formation in  

E-Print Network [OSTI]

troposphere and lower stratosphere. The model implements a first order scheme for resolving the aerosol size distribution within its geometric size10 sections, which efficiently suppresses numerical diffusion. We operate removes freshly nucleated particles by coagulation. The observation of high ultrafine aerosol

Paris-Sud XI, Université de

430

6, 32653319, 2006 Study aerosol with  

E-Print Network [OSTI]

ACPD 6, 3265­3319, 2006 Study aerosol with two emission inventories and time factors A. de Meij et in Europe to two different emission inventories and temporal distribution of emissions A. de Meij 1 , M Study aerosol with two emission inventories and time factors A. de Meij et al. Title Page Abstract

Paris-Sud XI, Université de

431

E-Print Network 3.0 - atmospheric diffusion Sample Search Results  

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

Horizontal transport in the atmosphere Dry and moist static energy Eddy vs. mean transport Horizontal... variations Radiative equilibrium temperature profile vs. actual...

432

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

SciTech Connect (OSTI)

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.

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

2014-05-23T23:59:59.000Z

433

AEROSOL PARTICLE COLLECTOR DESIGN STUDY  

SciTech Connect (OSTI)

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.

Lee, S; Richard Dimenna, R

2007-09-27T23:59:59.000Z

434

ARM - Field Campaign - Aerosol IOP  

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May JunDatastreamsmmcrcalgovInstrumentsrucLasDelivered‰PNGExperience4AJ01)3, 2010SeptemberInfrared SpectralgovCampaignsAerosol IOP

435

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.

436

ARM - Field Campaign - Two-Column Aerosol Project (TCAP): Airborne HSRL and  

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth (AOD) by Microtops Atmospheric Optical DepthgovCampaignsSpring(PROBE)govCampaignsTwo-Column AerosolRSP

437

Global observations of desert dust and biomass burning aerosols  

E-Print Network [OSTI]

Global observations of desert dust and biomass burning aerosols Martin de Graaf KNMI #12; Outline · Absorbing Aerosol Index - Theory · Absorbing Aerosol Index - Reality · Biomass burning.6 Biomass burning over Angola, 09 Sep. 2004 Absorbing Aerosol Index PMD image #12;biomass burning ocean

Graaf, Martin de

438

Climatology of aerosol optical depth in north?central Oklahoma: 19922008  

SciTech Connect (OSTI)

Aerosol optical depth (AOD) has been measured at the Atmospheric Radiation Measurement Program central facility near Lamont, Oklahoma, since the fall of 1992. Most of the data presented are from the multifilter rotating shadowband radiometer, a narrow?band, interference?filter Sun radiometer with five aerosol bands in the visible and near infrared; however, AOD measurements have been made simultaneously and routinely at the site by as many as three different types of instruments, including two pointing Sun radiometers. Scatterplots indicate high correlations and small biases consistent with earlier comparisons. The early part of this 16 year record had a disturbed stratosphere with residual Mt. Pinatubo aerosols, followed by the cleanest stratosphere in decades. As such, the last 13 years of the record reflect changes that have occurred predominantly in the troposphere. The field calibration technique is briefly described and compared to Langley calibrations from Mauna Loa Observatory. A modified cloudscreening technique is introduced that increases the number of daily averaged AODs retrieved annually to about 250 days compared with 175 days when a more conservative method was employed in earlier studies. AODs are calculated when the air mass is less than six; that is, when the Suns elevation is greater than 9.25. The more inclusive cloud screen and the use of most of the daylight hours yield a data set that can be used to more faithfully represent the true aerosol climate for this site. The diurnal aerosol cycle is examined month?by?month to assess the effects of an aerosol climatology on the basis of infrequent sampling such as that from satellites.

Michalsky, Joseph J.; Denn, Frederick; Flynn, Connor J.; Hodges, G. B.; Kiedron, Piotr; Koontz, Annette S.; Schlemmer, James; Schwartz, Stephen E.

2010-04-13T23:59:59.000Z

439

Optical, physical, and chemical properties of springtime aerosol over Barrow Alaska in 2008  

SciTech Connect (OSTI)

Airborne observations from four flights during the 2008 Indirect and Semi-Direct Aerosol Campaign (ISDAC) are used to examine some cloud-free optical, physical, and chemical properties of aerosol particles in the springtime Arctic troposphere. The number concentrations of particles larger than 0.12 ?m (Na>120), important for light extinction and cloud droplet formation, ranged from 15 to 2260 cm?3, with the higher Na>120 cases dominated by measurements from two flights of long-range transported biomass burning (BB) aerosols. The two other flights examined here document a relatively clean aerosol and an Arctic Haze aerosol impacted by larger particles largely composed of dust. For observations from the cleaner case and the BB cases, the particle light scattering coefficients at low relative humidity (RH<20%) increased nonlinearly with increasing Na>120, driven mostly by an increase in mean sizes of particles with increasing Na>120 (BB cases). For those three cases, particle light absorption coefficients also increased nonlinearly with increasing Na>120 and linearly with increasing submicron particle volume concentration. In addition to black carbon, brown carbon was estimated to have increased light absorption coefficients by 27% (450 nm wavelength) and 14% (550 nm) in the BB cases. For the case with strong dust influence, the absorption relative to submicron particle volume was small compared with the other cases. There was a slight gradient of Passive Cavity Aerosol Spectrometer Probe (PCASP) mean volume diameter (MVD) towards smaller sizes with increasing height, which suggests more scavenging of the more elevated particles, consistent with a typically longer lifetime of particles higher in the atmosphere. However, in approximately 10% of the cases, the MVD increased (>0.4 ?m) with increasing altitude, suggesting transport of larger fine particle mass (possibly coarse particle mass) at high levels over the Arctic. This may be because of transport of larger particles at higher elevations and relatively slow deposition to the surface.

Shantz, Nicole C.; Gultepe, Ismail; Andrews, Elisabeth; Zelenyuk, Alla; Earle, Michael; MacDonald, A. M.; Liu, Peter S.; Leaitch, W. R.

2014-03-06T23:59:59.000Z

440

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

E-Print Network [OSTI]

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

Tilstra, Gijsbert

Note: This page contains sample records for the topic "aerosols atmospheric profiling" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


441

Indirect and Semi-Direct Aerosol Campaign: The Impact of Arctic...  

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

Aerosol Campaign: The Impact of Arctic Aerosols on Clouds . Abstract: A comprehensive dataset of microphysical and radiative properties of aerosols and clouds in the arctic...

442

The behavior of constant rate aerosol reactors  

SciTech Connect (OSTI)

An aerosol reactor is a gaseous system in which fine particles are formed by chemical reaction in either a batch or flow process. The particle sizes of interest range from less than 10 angstrom (molecular clusters) to 10 ..mu..m. Such reactors may be operated to study the aerosol formation process, as in a smog reactor, or to generate a product such as a pigment or a catalytic aerosol. Aerosol reactors can be characterized by three temporal or spatial zones or regions of operation for batch and flow reactors, respectively. In zone I, chemical reaction results in the formation of condensable molecular products which nucleate and form very high concentrations of small particles. The number density depends on the concentration of preexisting aerosol. Zone II is a transition region in which the aerosol number concentration levels off as a result of hetergeneous condensation by the stable aerosol. In zone III coagulation becomes sufficiently rapid to reduce the particle number concentration. There may be a zone IV in which agglomerates form.

Friedlander, S.K.

1982-01-01T23:59:59.000Z

443

CARES: Carbonaceous Aerosol and Radiative Effects Study Science Plan  

SciTech Connect (OSTI)

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.

Zaveri, RA; Shaw, WJ; Cziczo, DJ

2010-05-27T23:59:59.000Z

444

Capstone Depleted Uranium Aerosols: Generation and Characterization  

SciTech Connect (OSTI)

In a study designed to provide an improved scientific basis for assessing possible health effects from inhaling depleted uranium (DU) aerosols, a series of DU penetrators was fired at an Abrams tank and a Bradley fighting vehicle. A robust sampling system was designed to collect aerosols in this difficult environment and continuously monitor the sampler flow rates. Aerosols collected were analyzed for uranium concentration and particle size distribution as a function of time. They were also analyzed for uranium oxide phases, particle morphology, and dissolution in vitro. The resulting data provide input useful in human health risk assessments.

Parkhurst, MaryAnn; Szrom, Fran; Guilmette, Ray; Holmes, Tom; Cheng, Yung-Sung; Kenoyer, Judson L.; Collins, John W.; Sanderson, T. Ellory; Fliszar, Richard W.; Gold, Kenneth; Beckman, John C.; Long, Julie

2004-10-19T23:59:59.000Z

445

Environmental radiation safety: source term modification by soil aerosols. Interim report  

SciTech Connect (OSTI)

The goal of this project is to provide information useful in estimating hazards related to the use of a pure refractory oxide of /sup 238/Pu as a power source in some of the space vehicles to be launched during the next few years. Although the sources are designed and built to withstand re-entry into the earth's atmosphere, and to impact with the earth's surface without releasing any plutonium, the possibility that such an event might produce aerosols composed of soil and /sup 238/PuO/sub 2/ cannot be absolutely excluded. This report presents the results of our most recent efforts to measure the degree to which the plutonium aerosol source term might be modified in a terrestrial environment. The five experiments described represent our best effort to use the original experimental design to study the change in the size distribution and concentration of a /sup 238/PuO/sub 2/ aerosol due to coagulation with an aerosol of clay or sandy loam soil.

Moss, O.R.; Allen, M.D.; Rossignol, E.J.; Cannon, W.C.

1980-08-01T23:59:59.000Z

446

Modeling LIDAR Detection of Biological Aerosols to Determine Optimum Implementation Strategy  

SciTech Connect (OSTI)

This report summarizes work performed for a larger multi-laboratory project named the Background Interferent Measurement and Standards project. While originally tasked to develop algorithms to optimize biological warfare agent detection using UV fluorescence LIDAR, the current uncertainties in the reported fluorescence profiles and cross sections the development of any meaningful models. It was decided that a better approach would be to model the wavelength-dependent elastic backscattering from a number of ambient background aerosol types, and compare this with that generated from representative sporulated and vegetative bacterial systems. Calculations in this report show that a 266, 355, 532 and 1064 nm elastic backscatter LIDAR experiment will allow an operator to immediately recognize when sulfate, VOC-based or road dust (silicate) aerosols are approaching, independent of humidity changes. It will be more difficult to distinguish soot aerosols from biological aerosols, or vegetative bacteria from sporulated bacteria. In these latter cases, the elastic scattering data will most likely have to be combined with UV fluorescence data to enable a more robust categorization.

Sheen, David M.; Aker, Pam M.

2007-09-19T23:59:59.000Z

447

Southern hemisphere tropospheric aerosol microphysics  

SciTech Connect (OSTI)

Aerosol particle size distribution data have been obtained in the southern hemisphere from approximately 4{degree}S to 44{degree}S and between ground level and 6 km, in the vicinity of eastern Australia. The relative shape of the free-tropospheric size distribution for particles with radii larger than approximately 0.04 {mu}m was found to be remarkably stable with time, altitude, and location for the autumn-winter periods considered. This was despite some large concentration changes which were found to be typical of the southeastern Australian coastal region. The majority of free-troposphere large particles were found to have sulfuric acid or lightly ammoniated sulfate morphology. Large particles in the boundary layer almost exclusively had a sea-salt morphology.

Gras, J.L. (Commonwealth Scientific and Industrial Research Organization, Aspendale (Australia))

1991-03-20T23:59:59.000Z

448

Aerosol composition, chemistry, and source characterization during the 2008 VOCALS Experiment  

SciTech Connect (OSTI)

Chemical composition of fine aerosol particles over the northern Chilean coastal waters was determined onboard the U.S. DOE G-1 aircraft during the VOCALS (VAMOS Ocean-Cloud-Atmosphere-Land Study) field campaign between October 16 and November 15, 2008. SO42-, NO3-, NH4+, and total organics (Org) were determined using an Aerodyne Aerosol Mass Spectrometer, and SO42-, NO3-, NH4+, Na+, Cl-, CH3SO3-, Mg2+, Ca2+, and K+ were determined using a particle-into-liquid sampler-ion chromatography technique. The results show the marine boundary layer (MBL) aerosol mass was dominated by non- sea-salt SO42- followed by Na+, Cl-, Org, NO3-, and NH4+, in decreasing importance; CH3SO3-, Ca2+, and K+ rarely exceeded their respective limits of detection. The SO42- aerosols were strongly acidic as the equivalent NH4+ to SO42- ratio was only {approx}0.25 on average. NaCl particles, presumably of sea-salt origin, showed chloride deficits but retained Cl- typically more than half the equivalency of Na+, and are externally mixed with the acidic sulfate aerosols. Nitrate was observed only on sea-salt particles, consistent with adsorption of HNO3 on sea-salt aerosols, responsible for the Cl- deficit. Dust particles appeared to play a minor role, judging from the small volume differences between that derived from the observed mass concentrations and that calculated based on particle size distributions. Because SO42- concentrations were substantial ({approx}0.5 - {approx}3 {micro}g/m3) with a strong gradient (highest near the shore), and the ocean-emitted dimethylsulfide and its unique oxidation product, CH3SO3-, were very low (i.e., {le} 40 parts per trillion and <0.05 {micro}g/m3, respectively), the observed SO42- aerosols are believed to be primarily of terrestrial origin. Back trajectory calculations indicate sulfur emissions from smelters and power plants along coastal regions of Peru and Chile are the main sources of these SO4- aerosols. However, compared to observations, model calculations appeared to underestimate sulfate concentrations based on an existing emission inventory. The agreement between observations and model predictions of CO as well as total sulfur is reexamined in this work with a new emission inventory made available recently.

Lee, Y.; Springston, S.; Jayne, J.; Wang, J.; Senum, G.; Hubbe, J.; Alexander, L.; Brioude, J.; Spak, S.; Mena-Carrasco, M.; Kleinman, L.; Daum, P.

2010-03-15T23:59:59.000Z

449

Radiative and climate impacts of absorbing aerosols  

E-Print Network [OSTI]

incident radiation are distinguished, and albedos for oceanOceans using multiple satellite datasets in conjunction with MACR (Monte Carlo Aerosol-Cloud-Radiation)ocean temperature is coupled with the rest of the climate system, the dimming of surface radiation

Zhu, Aihua

2010-01-01T23:59:59.000Z

450

CIRRICULUM VITAE: TOM BREIDER Atmospheric Chemistry Post-Doctoral Research Fellow  

E-Print Network [OSTI]

to changing anthropogenic and dynamic biogenic emissions of trace gases and aerosols. These chemistry and trace gas factors affecting the number concentration of atmospheric Aitken (Dp=50 nm) particles. Discuss., 3, 1185-1221, 2010 4) Hossani, R., M. P. Chipperfield, W. Feng, T. J. Breider, E. Atlas, S. A

Jacob, Daniel J.

451

Raman Lidar ProfilesTemperature (RLPROFTEMP) Value-Added Product  

SciTech Connect (OSTI)

The purpose of this document is to describe the Raman Lidar ProfilesTemperature (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.

Newsom, RK; Sivaraman, C; McFarlane, SA

2012-10-31T23:59:59.000Z

452

Aerosol fabrication methods for monodisperse nanoparticles  

DOE Patents [OSTI]

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.

Jiang, Xingmao; Brinker, C Jeffrey

2014-10-21T23:59:59.000Z

453

Development of plutonium aerosol fractionation system  

E-Print Network [OSTI]

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...

Mekala, Malla R.

1993-01-01T23:59:59.000Z

454

Electrically Driven Technologies for Radioactive Aerosol Abatement  

SciTech Connect (OSTI)

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.

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

2003-01-28T23:59:59.000Z

455

Case Study of Water-Soluble Metal Containing Organic Constituents of Biomass Burning Aerosol  

SciTech Connect (OSTI)

Natural and prescribed biomass fires are a major source of atmospheric aerosols that can persist in the atmosphere for long periods of time. Biomass burning aerosols (BBA) can be associated with long range transport of water soluble N?, S?, P?, and metal?containing species. In this study, BBA samples were collected using a particle?into?liquid sampler (PILS) from laboratory burns of vegetation collected on military bases in the southeastern and southwestern United States. The samples were then analyzed using high resolution electrospray ionization mass spectrometry (ESI/HR?MS) that enabled accurate mass measurements for hundreds of species with m/z values between 70 and 1000 and assignment of probable elemental formulae. Mg, Al, Ca, Cr, Mn, Fe, Ni, Cu, Zn, and Ba?containing organometallic species were identified. The results suggest that the biomass may have accumulated metal?containing species that were reemitted during biomass burning. Further research into the sources, persistence, and dispersion of metal?containing aerosols as well as their environmental effects is needed.

Chang-Graham, Alexandra L.; Profeta, Luisa Tm; Johnson, Timothy J.; Yokelson, Robert J.; Laskin, Alexander; Laskin, Julia

2011-01-10T23:59:59.000Z

456

Lidar Investigation of Tropical Nocturnal Boundary Layer Aerosols and Cloud Macrophysics  

SciTech Connect (OSTI)

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.

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

2013-10-01T23:59:59.000Z

457

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

SciTech Connect (OSTI)

In the last 100 years, the Earth has warmed by about 1F, 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.

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

2010-05-12T23:59:59.000Z

458

E-Print Network 3.0 - aerosol chemical vapor Sample Search Results  

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

chemical and microphysical properties influence aerosol optical properties and radiative effects... distribution of aerosol extensive and intensive properties will aid ......

459

Analyzing Surface Solar Flux Data in Oregon for Changes Due to Aerosols Laura D. Riihimaki1, Frank E. Vignola1, Charles N. Long2, James A. Coakley Jr.3 1 University of Oregon Solar Radiation Monitoring Lab 2 Pacific Northwest National Laboratory 3 Oregon State University, College of Oceanic and Atmospheric Sciences  

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth (AOD)ProductssondeadjustsondeadjustAbout theOFFICEAmes Laboratory Site| Department SeptemberSignificant

460

Development of Soft Ionization for Particulate Organic Detection with the Aerodyne Aerosol Mass Spectrometer  

SciTech Connect (OSTI)

During this DOE SBIR Phase II project, we have successfully developed several soft ionization techniques, i.e., ionization schemes which involve less fragmentation of the ions, for use with the Aerodyne time-of-flight aerosol mass spectrometer (ToF-AMS). Vacuum ultraviolet single photon ionization was demonstrated in the laboratory and deployed in field campaigns. Vacuum ultraviolet single photon ionization allows better identification of organic species in aerosol particles as shown in laboratory experiments on single component particles, and in field measurements on complex multi-component particles. Dissociative electron attachment with lower energy electrons (less than 30 eV) was demonstrated in the measurement of particulate organics in chamber experiments in Switzerland, and is now a routine approach with AMS systems configured for bipolar, negative ion detection. This technique is particularly powerful for detection of acidic and other highly oxygenated secondary organic aerosol (SOA) chemical functionality. Low energy electron ionization (10 to 12 eV) is also a softer ionization approach routinely available to AMS users. Finally, Lithium ion attachment has been shown to be sensitive to more alkyl-like chemical functionality in SOA. Results from Mexico City are particularly exciting in observing changes in SOA molecular composition under different photochemical/meteorological conditions. More recent results detecting biomass burns at the Montana fire lab have demonstrated quantitative and selective detection of levoglucosan. These soft ionization techniques provide the ToF-AMS with better capability for identifying organic species in ambient atmospheric aerosol particles. This, in turn, will allow more detailed study of the sources, transformations and fate of organic-containing aerosol.

Trimborn, A; Williams, L R; Jayne, J T; Worsnop, D R

2008-06-19T23:59:59.000Z

Note: This page contains sample records for the topic "aerosols atmospheric profiling" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


461

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutronEnvironmentZIRKLE FRUITYear 1

462

Effect of Hydrophobic Primary Organic Aerosols on Secondary Organic Aerosol  

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed NewcatalystNeutronEnvironmentZIRKLE FRUITYear

463

Application of computational fluid dynamics to aerosol sampling and concentration  

E-Print Network [OSTI]

An understanding of gas-liquid two-phase interactions, aerosol particle deposition, and heat transfer is needed. Computational Fluid Dynamics (CFD) is becoming a powerful tool to predict aerosol behavior for related design work. In this study...

Hu, Shishan

2009-05-15T23:59:59.000Z

464

Aerosol beam-focus laser-induced plasma spectrometer device  

DOE Patents [OSTI]

An apparatus for detecting elements in an aerosol includes an aerosol beam focuser for concentrating aerosol into an aerosol beam; a laser for directing a laser beam into the aerosol beam to form a plasma; a detection device that detects a wavelength of a light emission caused by the formation of the plasma. The detection device can be a spectrometer having at least one grating and a gated intensified charge-coupled device. The apparatus may also include a processor that correlates the wavelength of the light emission caused by the formation of the plasma with an identity of an element that corresponds to the wavelength. Furthermore, the apparatus can also include an aerosol generator for forming an aerosol beam from bulk materials. A method for detecting elements in an aerosol is also disclosed.

Cheng, Meng-Dawn (Oak Ridge, TN)

2002-01-01T23:59:59.000Z

465

aerosol particle penetration: Topics by E-print Network  

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

the subsequent aerosol penetration performance through these tubes were conducted for a aerosol particle size range of 5 nm to 20 nm and a flow rate range of 28 Lmin to 169.9...

466

Effects of operating conditions on a heat transfer fluid aerosol  

E-Print Network [OSTI]

of heat transfer fluid aerosols from process leaks. To simulate industrial leaks, aerosol formation from a plain orifice into ambient air is studied by measuring liquid drop sizes and size distributions at various distances from an orifice. Measurements...

Sukmarg, Passaporn

2000-01-01T23:59:59.000Z

467

Spectrophotometric Resolution of Stellar Atmospheres with Microlensing  

E-Print Network [OSTI]

Microlensing is a powerful tool for studying stellar atmospheres because as the source crosses regions of formally infinite magnification (caustics) the surfaceof the star is resolved, thereby allowing one to measure the radial intensity profile, both photometrically and spectroscopically. However, caustic crossing events are relatively rare, and monitoring them requires intensive application of telescope resources. It is therefore essential that the observational parameters needed to accurately measure the intensity profile are quantified. We calculate the expected errors in the recovered radial intensity profile as a function of the unlensed flux, source radius, spatial resolution the recovered intensity profile, and caustic crossing time for the two principle types of caustics: point-mass and binary lenses. We demonstrate that for both cases there exist simple scaling relations between these parameters and the resultant errors. We find that the error as a function of the spatial resolution of the recovered profile, parameterized by the number of radial bins, increases as $N_R^{3/2}$, considerably faster than the naive $N_R^{1/2}$ expectation. Finally, we discuss the relative advantages of binary caustic-crossing events and point-lens events. Binary events are more common, easier to plan for, and provide more homogeneous information about the stellar atmosphere. However, a sub-class of point-mass events with low impact parameters can provide dramatically more information provided that they can be recognized in time to initiate observations.

B. Scott Gaudi; Andrew Gould

1998-02-14T23:59:59.000Z

468

Atmospheric Radiation Measurement Program Science Plan  

SciTech Connect (OSTI)

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.

Ackerman, T

2004-10-31T23:59:59.000Z

469

Atmospheric profiles of CO? as integrators of regional scale exchange  

E-Print Network [OSTI]

not simulate uncultivated land associated with agriculture, which in Scotland represents 36 % of agricultural holdings. Therefore, uncultivated land components may provide an explanation for the increase in model-data error. Interannual variation in weather...

Smallman, Thomas Luke

2014-06-30T23:59:59.000Z

470

Analyzing Surface Solar Flux Data in Oregon for Changes Due to Aerosols Laura D. Riihimaki1, Frank E. Vignola1, Charles N. Long2, James A. Coakley Jr.3 1 University of Oregon Solar Radiation Monitoring Lab 2 Pacific Northwest National Laboratory 3 Oregon State University, College of Oceanic and Atmospheric Sciences  

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth (AOD)ProductssondeadjustsondeadjustAbout theOFFICEAmes Laboratory Site| Department SeptemberSignificant76 1980

471

ARM Aerosol Working Group Meeting  

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth (AOD)Productssondeadjustsondeadjust Documentation DataProductswsicloudwsicloudsummarygifAOS ProcessingReport

472

ARM Aerosol Working Group Meeting  

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth (AOD)Productssondeadjustsondeadjust Documentation DataProductswsicloudwsicloudsummarygifAOS ProcessingReport

473

ARM Aerosol Working Group Meeting  

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth (AOD)Productssondeadjustsondeadjust Documentation DataProductswsicloudwsicloudsummarygifAOS

474

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)]

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.

Williams, Christopher; Jensen, Mike

475

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

SciTech Connect (OSTI)

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.

Williams, Christopher; Jensen, Mike

2012-11-06T23:59:59.000Z

476

Project of Aerosol Optical Depth Change in South America  

E-Print Network [OSTI]

AerosolDepth Brazil Bolivia French Guiana Suriname Guyana Venezuela Colombia Ecuador Peru Chile Argentina Suriname Guyana Venezuela Colombia Ecuador Peru Chile Argentina Paraguay Uruguay #12;Statistics of Aerosol M ean D ec 01 to 06 Mean Month AerosolDepth Brazil Bolivia French Guiana Suriname Guyana Venezuela

Frank, Thomas D.

477

Sulfuric acid deposition from stratospheric geoengineering with sulfate aerosols  

E-Print Network [OSTI]

aerosols can potentially result in an increase in acid deposition. [4] Acid rain has been studiedSulfuric acid deposition from stratospheric geoengineering with sulfate aerosols Ben Kravitz,1 Alan limit of hydration of all sulfate aerosols into sulfuric acid. For annual injection of 5 Tg of SO2

Robock, Alan

478

Organic and Inorganic Aerosol Below-Cloud Scavenging by  

E-Print Network [OSTI]

concentrations, with an average gravimetric PM1.0 of 8.2 ( 1.6 µg m-3 and an average Fourier transform infrared-rinsing behavior was unaffected by source type. The aerosol OM was hydrophilic throughout the sampling period the description of aerosol lifetimes in global models. Introduction Wet and dry deposition of aerosol particles

Russell, Lynn