Science.gov

Sample records for aerosol containment experiments

  1. Experiences from Occupational Exposure Limits Set on Aerosols Containing Allergenic Proteins

    PubMed Central

    Nielsen, Gunnar D.

    2012-01-01

    Occupational exposure limits (OELs) together with determined airborne exposures are used in risk assessment based managements of occupational exposures to prevent occupational diseases. In most countries, OELs have only been set for few protein-containing aerosols causing IgE-mediated allergies. They comprise aerosols of flour dust, grain dust, wood dust, natural rubber latex, and the subtilisins, which are proteolytic enzymes. These aerosols show dose-dependent effects and levels have been established, where nearly all workers may be exposed without adverse health effects, which are required for setting OELs. Our aim is to analyse prerequisites for setting OELs for the allergenic protein-containing aerosols. Opposite to the key effect of toxicological reactions, two thresholds, one for the sensitization phase and one for elicitation of IgE-mediated symptoms in sensitized individuals, are used in the OEL settings. For example, this was the case for flour dust, where OELs were based on dust levels due to linearity between flour dust and its allergen levels. The critical effects for flour and grain dust OELs were different, which indicates that conclusion by analogy (read-across) must be scientifically well founded. Except for subtilisins, no OEL have been set for other industrial enzymes, where many of which are high volume chemicals. For several of these, OELs have been proposed in the scientific literature during the last two decades. It is apparent that the scientific methodology is available for setting OELs for proteins and protein-containing aerosols where the critical effect is IgE sensitization and IgE-mediated airway diseases. PMID:22843406

  2. Note: Design and development of wireless controlled aerosol sampling network for large scale aerosol dispersion experiments

    SciTech Connect

    Gopalakrishnan, V.; Subramanian, V.; Baskaran, R.; Venkatraman, B.

    2015-07-15

    Wireless based custom built aerosol sampling network is designed, developed, and implemented for environmental aerosol sampling. These aerosol sampling systems are used in field measurement campaign, in which sodium aerosol dispersion experiments have been conducted as a part of environmental impact studies related to sodium cooled fast reactor. The sampling network contains 40 aerosol sampling units and each contains custom built sampling head and the wireless control networking designed with Programmable System on Chip (PSoC™) and Xbee Pro RF modules. The base station control is designed using graphical programming language LabView. The sampling network is programmed to operate in a preset time and the running status of the samplers in the network is visualized from the base station. The system is developed in such a way that it can be used for any other environment sampling system deployed in wide area and uneven terrain where manual operation is difficult due to the requirement of simultaneous operation and status logging.

  3. Note: Design and development of wireless controlled aerosol sampling network for large scale aerosol dispersion experiments

    NASA Astrophysics Data System (ADS)

    Gopalakrishnan, V.; Subramanian, V.; Baskaran, R.; Venkatraman, B.

    2015-07-01

    Wireless based custom built aerosol sampling network is designed, developed, and implemented for environmental aerosol sampling. These aerosol sampling systems are used in field measurement campaign, in which sodium aerosol dispersion experiments have been conducted as a part of environmental impact studies related to sodium cooled fast reactor. The sampling network contains 40 aerosol sampling units and each contains custom built sampling head and the wireless control networking designed with Programmable System on Chip (PSoC™) and Xbee Pro RF modules. The base station control is designed using graphical programming language LabView. The sampling network is programmed to operate in a preset time and the running status of the samplers in the network is visualized from the base station. The system is developed in such a way that it can be used for any other environment sampling system deployed in wide area and uneven terrain where manual operation is difficult due to the requirement of simultaneous operation and status logging.

  4. THERMODYNAMIC MODELING OF LIQUID AEROSOLS CONTAINING DISSOLVED ORGANICS AND ELECTROLYTES

    EPA Science Inventory

    Many tropospheric aerosols contain large fractions of soluble organic material, believed to derive from the oxidation of precursors such alpha-pinene. The chemical composition of aerosol organic matter is complex and not yet fully understood.

    The key properties of solu...

  5. MELCOR 1. 8. 1 assessment: LACE aerosol experiment LA4

    SciTech Connect

    Kmetyk, L.N.

    1991-09-01

    The MELCOR code has been used to simulate LACE aerosol experiment LA4. In this test, the behavior of single- and double-component, hygroscopic and nonhygroscopic, aerosols in a condensing environment was monitored. Results are compared to experimental data, and to CONTAIN calculations. Sensitivity studies have been done on time step effects and machine dependencies; thermal/hydraulic parameters such as condensation on heat structures and on pool surface, and radiation heat transfer; and aerosol parameters such as number of MAEROS components and sections assumed, the degree to which plated aerosols are washed off heat structures by condensate film draining, and the effect of non-default values for shape factors and diameter limits. 9 refs., 50 figs., 13 tabs.

  6. Note: Design and development of wireless controlled aerosol sampling network for large scale aerosol dispersion experiments.

    PubMed

    Gopalakrishnan, V; Subramanian, V; Baskaran, R; Venkatraman, B

    2015-07-01

    Wireless based custom built aerosol sampling network is designed, developed, and implemented for environmental aerosol sampling. These aerosol sampling systems are used in field measurement campaign, in which sodium aerosol dispersion experiments have been conducted as a part of environmental impact studies related to sodium cooled fast reactor. The sampling network contains 40 aerosol sampling units and each contains custom built sampling head and the wireless control networking designed with Programmable System on Chip (PSoC™) and Xbee Pro RF modules. The base station control is designed using graphical programming language LabView. The sampling network is programmed to operate in a preset time and the running status of the samplers in the network is visualized from the base station. The system is developed in such a way that it can be used for any other environment sampling system deployed in wide area and uneven terrain where manual operation is difficult due to the requirement of simultaneous operation and status logging. PMID:26233420

  7. The salting behavior of glyoxal in model aerosols containing sulfate

    NASA Astrophysics Data System (ADS)

    Waxman, Eleanor; Kampf, Christopher; Slowik, Jay; Dommen, Josef; Pfaffenberger, Lisa; Praplan, Arnaud; Prevot, Andre; Baltensperger, Urs; Hoffmann, Thorsten; Volkamer, Rainer

    2013-04-01

    Glyoxal, the smallest alpha-dicarbonyl, is a ubiquitous component of biogenic environments and urban, arctic, and marine atmospheres. An increasing body of evidence finds small water soluble and polar oxygenated hydrocarbons (OVOC) like glyoxal in the condensed phase despite their high vapor pressures. It is generally believed that multiphase chemical reactions in cloud or aerosol water form soluble products with lower vapor pressures, and that this lowering of the vapor pressure is the primary cause for the enhanced partitioning. However, our data shows that this could be due to electrostatic forces instead. We have performed a series of simulation chamber experiments to quantify for the first time the time-resolved evolution of glyoxal partitioning to aqueous model aerosols containing sulfate. These measurements show an exponential increase in Henry's law constants with seed particle salt concentrations. This exponential increase is found to be independent of the presence or absence of organics in the seed particles, and can be explained by means of a single parameter, the salting constant K_S, to predict the partitioning of glyoxal over a wide range of environmental conditions (cloud water and concentrated salt solutions of aerosol water). The formalism that we find best explains our data builds on the theory developed by Setschenow in the late 19th century. It is known to the limnology community, but to our knowledge has not previously been used to describe aqueous systems in the atmosphere (aerosols or cloud droplets). The rapid and high monomer partitioning suggests that electrostatic forces triggered by the high dipole moment of glyoxal, rather than vapor pressure, are at the core of the mechanism that causes the high partitioning. This high abundance of glyoxal monomers is compared with oligomeric reservoirs and irreversible reaction pathways (NH4 or OH radical reactions), and representations for use in atmospheric models are discussed that can explain most

  8. Characteristics of atmospheric aerosols containing heavy metals measured on Fukue Island, Japan

    NASA Astrophysics Data System (ADS)

    Hidemori, Takehiro; Nakayama, Tomoki; Matsumi, Yutaka; Kinugawa, Takashi; Yabushita, Akihiro; Ohashi, Masafumi; Miyoshi, Takao; Irei, Satoshi; Takami, Akinori; Kaneyasu, Naoki; Yoshino, Ayako; Suzuki, Ryota; Yumoto, Yayoi; Hatakeyama, Shiro

    2014-11-01

    To investigate transport and chemical compositions of fine aerosols in the East Asian region, aerosol chemical components and their mixing states were measured at Fukue Island in the spring of 2010. Off-line chemical analyses using an ion chromatographic analyzer and an inductively coupled plasma-mass spectrometer for the aerosols sampled by a high volume sampler have also been conducted. The mixing state and temporal variation of number concentrations of the particles containing lead (Pb) and vanadium (V) were studied by using a laser ionization single-particle aerosol mass spectrometer (LISPA-MS). The temporal variation of number concentrations of particles containing Pb measured by the LISPA-MS is well consistent with those obtained by the chemical analysis of the aerosols sampled by the high volume sampler. The Pb-containing particles were classified into four types from the statistical analysis on the basis of the single-particle mass spectra with assists of laboratory experiments. It is estimated that 52% of observed particles containing Pb were originated from coal combustion. The concentration-weighted trajectory (CWT) analysis suggests that these particles are mainly transported from China continent. The V-containing particles were classified into three types. The 41% of V-containing particles were internally mixed with sea salt and the result of CWT analysis suggests that the potentially anthropogenic V-containing particles possibility emitted from ships are mixing with sea salt in the region that is highly loaded with sea salt in the Pacific Ocean.

  9. Laboratory Experiments and Instrument Intercomparison Studies of Carbonaceous Aerosol Particles

    SciTech Connect

    Davidovits, Paul

    2015-10-20

    Aerosols containing black carbon (and some specific types of organic particulate matter) directly absorb incoming light, heating the atmosphere. In addition, all aerosol particles backscatter solar light, leading to a net-cooling effect. Indirect effects involve hydrophilic aerosols, which serve as cloud condensation nuclei (CCN) that affect cloud cover and cloud stability, impacting both atmospheric radiation balance and precipitation patterns. At night, all clouds produce local warming, but overall clouds exert a net-cooling effect on the Earth. The effect of aerosol radiative forcing on climate may be as large as that of the greenhouse gases, but predominantly opposite in sign and much more uncertain. The uncertainties in the representation of aerosol interactions in climate models makes it problematic to use model projections to guide energy policy. The objective of our program is to reduce the uncertainties in the aerosol radiative forcing in the two areas highlighted in the ASR Science and Program Plan. That is, (1) addressing the direct effect by correlating particle chemistry and morphology with particle optical properties (i.e. absorption, scattering, extinction), and (2) addressing the indirect effect by correlating particle hygroscopicity and CCN activity with particle size, chemistry, and morphology. In this connection we are systematically studying particle formation, oxidation, and the effects of particle coating. The work is specifically focused on carbonaceous particles where the uncertainties in the climate relevant properties are the highest. The ongoing work consists of laboratory experiments and related instrument inter-comparison studies both coordinated with field and modeling studies, with the aim of providing reliable data to represent aerosol processes in climate models. The work is performed in the aerosol laboratory at Boston College. At the center of our laboratory setup are two main sources for the production of aerosol particles: (a

  10. AEROSOL CHARACTERIZATION WITH CENTRIFUCAL AEROSOL SPECTROMETERS: THEORY AND EXPERIMENT

    EPA Science Inventory

    A general mathematical model describing the motion of particles in aerosol centrifuges has been developed. t has been validated by comparisons of theoretically predicted calibration sites with experimental data from tests sizing aerosols in instruments of three different spiral d...

  11. LMFBR source term experiments in the Fuel Aerosol Simulant Test (FAST) facility

    SciTech Connect

    Petrykowski, J.C.; Longest, A.W.

    1985-01-01

    The transport of uranium dioxide (UO/sub 2/) aerosol through liquid sodium was studied in a series of ten experiments in the Fuel Aerosol Simulant Test (FAST) facility at Oak Ridge National Laboratory (ORNL). The experiments were designed to provide a mechanistic basis for evaluating the radiological source term associated with a postulated, energetic core disruptive accident (CDA) in a liquid metal fast breeder reactor (LMFBR). Aerosol was generated by capacitor discharge vaporization of UO/sub 2/ pellets which were submerged in a sodium pool under an argon cover gas. Measurements of the pool and cover gas pressures were used to study the transport of aerosol contained by vapor bubbles within the pool. Samples of cover gas were filtered to determine the quantity of aerosol released from the pool. The depth at which the aerosol was generated was found to be the most critical parameter affecting release. The largest release was observed in the baseline experiment where the sample was vaporized above the sodium pool. In the nine ''undersodium'' experiments aerosol was generated beneath the surface of the pool at depths varying from 30 to 1060 mm. The mass of aerosol released from the pool was found to be a very small fraction of the original specimen. It appears that the bulk of aerosol was contained by bubbles which collapsed within the pool. 18 refs., 11 figs., 4 tabs.

  12. SAGE II inversion algorithm. [Stratospheric Aerosol and Gas Experiment

    NASA Technical Reports Server (NTRS)

    Chu, W. P.; Mccormick, M. P.; Lenoble, J.; Brogniez, C.; Pruvost, P.

    1989-01-01

    The operational Stratospheric Aerosol and Gas Experiment II multichannel data inversion algorithm is described. Aerosol and ozone retrievals obtained with the algorithm are discussed. The algorithm is compared to an independently developed algorithm (Lenoble, 1989), showing that the inverted aerosol and ozone profiles from the two algorithms are similar within their respective uncertainties.

  13. 10 CFR 30.20 - Gas and aerosol detectors containing byproduct material.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 10 Energy 1 2011-01-01 2011-01-01 false Gas and aerosol detectors containing byproduct material... LICENSING OF BYPRODUCT MATERIAL Exemptions § 30.20 Gas and aerosol detectors containing byproduct material... distribution gas and aerosol detectors containing byproduct material, any person is exempt from...

  14. 10 CFR 30.20 - Gas and aerosol detectors containing byproduct material.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 10 Energy 1 2012-01-01 2012-01-01 false Gas and aerosol detectors containing byproduct material... LICENSING OF BYPRODUCT MATERIAL Exemptions § 30.20 Gas and aerosol detectors containing byproduct material... distribution gas and aerosol detectors containing byproduct material, any person is exempt from...

  15. 10 CFR 30.20 - Gas and aerosol detectors containing byproduct material.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 10 Energy 1 2014-01-01 2014-01-01 false Gas and aerosol detectors containing byproduct material... LICENSING OF BYPRODUCT MATERIAL Exemptions § 30.20 Gas and aerosol detectors containing byproduct material... distribution gas and aerosol detectors containing byproduct material, any person is exempt from...

  16. 10 CFR 30.20 - Gas and aerosol detectors containing byproduct material.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 10 Energy 1 2013-01-01 2013-01-01 false Gas and aerosol detectors containing byproduct material... LICENSING OF BYPRODUCT MATERIAL Exemptions § 30.20 Gas and aerosol detectors containing byproduct material... distribution gas and aerosol detectors containing byproduct material, any person is exempt from...

  17. 10 CFR 30.20 - Gas and aerosol detectors containing byproduct material.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 10 Energy 1 2010-01-01 2010-01-01 false Gas and aerosol detectors containing byproduct material... LICENSING OF BYPRODUCT MATERIAL Exemptions § 30.20 Gas and aerosol detectors containing byproduct material... distribution gas and aerosol detectors containing byproduct material, any person is exempt from...

  18. Online Aerosol Mass Spectrometry of Single Micrometer-Sized Particles Containing Poly(ethylene glycol)

    SciTech Connect

    Bogan, M J; Patton, E; Srivastava, A; Martin, S; Fergenson, D; Steele, P; Tobias, H; Gard, E; Frank, M

    2006-10-25

    Analysis of poly(ethylene glycol)(PEG)-containing particles by online single particle aerosol mass spectrometers equipped with laser desorption ionization (LDI) is reported. We demonstrate that PEG-containing particles are useful in the development of aerosol mass spectrometers because of their ease of preparation, low cost, and inherently recognizable mass spectra. Solutions containing millimolar quantities of PEGs were nebulized and, after drying, the resultant micrometer-sized PEG containing particles were sampled. LDI (266 nm) of particles containing NaCl and PEG molecules of average molecular weight <500 generated mass spectra reminiscent of mass spectra of PEG collected by other MS schemes including the characteristic distribution of positive ions (Na{sup +} adducts) separated by the 44 Da of the ethylene oxide units separating each degree of polymerization. PEGs of average molecular weight >500 were detected from particles that also contained t the tripeptide tyrosine-tyrosine-tyrosine or 2,5-dihydroxybenzoic acid, which were added to nebulized solutions to act as matrices to assist LDI using pulsed 266 nm and 355 nm lasers, respectively. Experiments were performed on two aerosol mass spectrometers, one reflectron and one linear, that each utilize two time-of-flight mass analyzers to detect positive and negative ions created from a single particle. PEG-containing particles are currently being employed in the optimization of our bioaerosol mass spectrometers for the application of measurements of complex biological samples, including human effluents, and we recommend that the same strategies will be of great utility to the development of any online aerosol LDI mass spectrometer platform.

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

    NASA Astrophysics Data System (ADS)

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

    2014-05-01

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

  20. 21 CFR 700.16 - Use of aerosol cosmetic products containing zirconium.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 7 2010-04-01 2010-04-01 false Use of aerosol cosmetic products containing... SERVICES (CONTINUED) COSMETICS GENERAL Requirements for Specific Cosmetic Products § 700.16 Use of aerosol... in cosmetics and/or cosmetics that are also drugs, as, for example, aerosol antiperspirants....

  1. The Charged Aerosol Release Experiment (CARE) Program

    NASA Astrophysics Data System (ADS)

    Bernhardt, Paul; Scales, Wayne; Sternovsky, Zoltan; Kelley, Michael; Hysell, David; Holzworth, Robert

    A new experiment called the Charged Aerosol Release Experiment (CARE) employs the release of dust in the upper atmosphere to form a dusty plasma in space. Two solid rocket motors strapped side-by-side in opposition will provide a pin-wheel high speed dust dispenser for the CARE experiment. A spherical dust cloud will form as a radial expansion around the CARE dust release module. The release will occur between 200 and 250 km altitude in the F-region where the 10 to 1000 nm diameter particles will become charged by electron attachment. As the charged dust particle stream through the ionosphere, plasma irregularities will be produced by streaming and fluid plasma instabilities. The plasma turbulence will driven by large electric fields at the surface of the cloud resulting from the separation of unmagnetized negatively charge dust from the background positive ions which are tied to magnetic field lines. In addition, two stream instabilities from the charge particles moving through the plasma will cause plasma wave structures. The effects of the CARE dust release will be diagnosed with in situ electric field booms, dust detectors, and Langmuir probes. Remote sensing of the CARE release will involve ground backscatter radars in the HF, VHF, and UHF frequency ranges. At late times, the dust cloud will settle into the mesosphere where an artificial mesospheric cloud will be formed. Satellite imagery using the AIM satellite will measure the long-term dispersal of the artificial dust cloud. The results of the CARE experiment will be compared with radar, optical and rocket measurements of natural polar mesospheric clouds.

  2. Aerosol effects and corrections in the Halogen Occultation Experiment

    NASA Technical Reports Server (NTRS)

    Hervig, Mark E.; Russell, James M., III; Gordley, Larry L.; Daniels, John; Drayson, S. Roland; Park, Jae H.

    1995-01-01

    The eruptions of Mt. Pinatubo in June 1991 increased stratospheric aerosol loading by a factor of 30, affecting chemistry, radiative transfer, and remote measurements of the stratosphere. The Halogen Occultation Experiment (HALOE) instrument on board Upper Atmosphere Research Satellite (UARS) makes measurements globally for inferring profiles of NO2, H2O, O3, HF, HCl, CH4, NO, and temperature in addition to aerosol extinction at five wavelengths. Understanding and removing the aerosol extinction is essential for obtaining accurate retrievals from the radiometer channels of NO2, H2O and O3 in the lower stratosphere since these measurements are severely affected by contaminant aerosol absorption. If ignored, aerosol absorption in the radiometer measurements is interpreted as additional absorption by the target gas, resulting in anomalously large mixing ratios. To correct the radiometer measurements for aerosol effects, a retrieved aerosol extinction profile is extrapolated to the radiometer wavelengths and then included as continuum attenuation. The sensitivity of the extrapolation to size distribution and composition is small for certain wavelength combinations, reducing the correction uncertainty. The aerosol corrections extend the usable range of profiles retrieved from the radiometer channels to the tropopause with results that agree well with correlative measurements. In situations of heavy aerosol loading, errors due to aerosol in the retrieved mixing ratios are reduced to values of about 15, 25, and 60% in H2O, O3, and NO2, respectively, levels that are much less than the correction magnitude.

  3. Beijing Olympics as an aerosol field experiment

    NASA Astrophysics Data System (ADS)

    Cermak, J.; Knutti, R.

    2009-05-01

    During the 2008 Olympic Summer Games, emission reductions were enforced in Beijing to improve air quality. Here we explore their effect on the regional aerosol load. We compare satellite-retrieved aerosol optical thickness (AOT) of that period with previous years, both in absolute terms and in a neural network approach taking into account the meteorological conditions. A statistically significant reduction of aerosol load is found in Beijing that decreases in magnitude and significance with increasing region size. Locally, the aerosol load (log(AOT)) was about 0.4 to 0.75 standard deviations below the levels expected for the prevailing meteorological situation. The small size of this effect relative to meteorological variability highlights the importance of regional aerosol transport.

  4. Aerosol Performance and Stability of Liposomes Containing Ciprofloxacin Nanocrystals

    PubMed Central

    Wu, Huiying; Gonda, Igor; Chan, Hak-Kim

    2015-01-01

    Abstract Background: Previously we showed that the release properties of a liposomal ciprofloxacin (CFI) formulation could be attenuated by incorporation of drug nanocrystals within the vesicles. Rather than forming these drug nanocrystals during drug loading, they were created post manufacture simply by freezing and thawing the formulation. The addition of surfactant to CFI, either polysorbate 20 or Brij 30, provided an additional means to modify the release profile or incorporate an immediate-release or ‘burst’ component as well. The goal of this study was to develop a CFI formulation that retained its nanocrystalline morphology and attenuated release profile after delivery as an inhaled aerosol. Methods: Preparations of 12.5 mg/mL CFI containing 90 mg/mL sucrose and 0.1% polysorbate 20 were formulated between pH 4.6 to 5.9, stored frozen, and thawed prior to use. These thawed formulations, before and after mesh nebulization, and after subsequent refrigerated storage for up to 6 weeks, were characterized in terms of liposome structure by cryogenic transmission electron microscopy (cryo-TEM) imaging, vesicle size by dynamic light scattering, pH, drug encapsulation by centrifugation-filtration, and in vitro release (IVR) performance. Results: Within the narrower pH range of 4.9 to 5.3, these 12.5 mg/mL liposomal ciprofloxacin formulations containing 90 mg/mL sucrose and 0.1% polysorbate 20 retained their physicochemical stability for an additional 3 months refrigerated storage post freeze-thaw, were robust to mesh nebulization maintaining their vesicular form containing nanocrystalline drug and an associated slower release profile, and formed respirable aerosols with a mass median aerodynamic diameter (MMAD) of ∼3.9 μm and a geometric standard deviation (GSD) of ∼1.5. Conclusions: This study demonstrates that an attenuated release liposomal ciprofloxacin formulation can be created through incorporation of drug nanocrystals in response to freeze

  5. Formation of highly oxygenated organic aerosol in the atmosphere: Insights from the Finokalia Aerosol Measurement Experiments

    NASA Astrophysics Data System (ADS)

    Hildebrandt, Lea; Kostenidou, Evangelia; Mihalopoulos, Nikos; Worsnop, Douglas R.; Donahue, Neil M.; Pandis, Spyros N.

    2010-12-01

    Aged organic aerosol (OA) was measured at a remote coastal site on the island of Crete, Greece during the Finokalia Aerosol Measurement Experiments (FAME-08 and FAME-09), which were part of the EUCAARI intensive campaigns. Quadrupole aerosol mass spectrometers (Q-AMSs) were employed to measure the size-resolved chemical composition of non-refractory submicron aerosol (NR-PM1), and to estimate the extent of oxidation of the OA. The experiments provide unique insights into ambient oxidation of aerosol by measuring at the same site but under different photochemical conditions. NR-PM1 concentrations were about a factor of three lower during FAME-09 (winter) than during FAME-08 (summer). The OA sampled was significantly less oxidized and more variable in composition during the winter than during the early summer. Lower OH concentrations in the winter were the main difference between the two campaigns, suggesting that atmospheric formation of highly oxygenated OA is associated with homogeneous photochemical aging.

  6. 21 CFR 700.16 - Use of aerosol cosmetic products containing zirconium.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 7 2011-04-01 2010-04-01 true Use of aerosol cosmetic products containing... SERVICES (CONTINUED) COSMETICS GENERAL Requirements for Specific Cosmetic Products § 700.16 Use of aerosol cosmetic products containing zirconium. (a) Zirconium-containing complexes have been used as an...

  7. 21 CFR 700.16 - Use of aerosol cosmetic products containing zirconium.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 7 2012-04-01 2012-04-01 false Use of aerosol cosmetic products containing... SERVICES (CONTINUED) COSMETICS GENERAL Requirements for Specific Cosmetic Products § 700.16 Use of aerosol cosmetic products containing zirconium. (a) Zirconium-containing complexes have been used as an...

  8. 21 CFR 700.16 - Use of aerosol cosmetic products containing zirconium.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 7 2014-04-01 2014-04-01 false Use of aerosol cosmetic products containing... SERVICES (CONTINUED) COSMETICS GENERAL Requirements for Specific Cosmetic Products § 700.16 Use of aerosol cosmetic products containing zirconium. (a) Zirconium-containing complexes have been used as an...

  9. Aged organic aerosol in the Eastern Mediterranean: the Finokalia aerosol measurement experiment-2008

    NASA Astrophysics Data System (ADS)

    Hildebrandt, L.; Engelhart, G. J.; Mohr, C.; Kostenidou, E.; Lanz, V. A.; Bougiatioti, A.; Decarlo, P. F.; Prévôt, A. S. H.; Baltensperger, U.; Mihalopoulos, N.; Donahue, N. M.; Pandis, S. N.

    2010-01-01

    Aged organic aerosol (OA) was measured at a remote coastal site on the island of Crete, Greece during the Finokalia Aerosol Measurement Experiment-2008 (FAME-2008), which was part of the EUCAARI intensive campaign of May 2008. The site at Finokalia is influenced by air masses from different source regions, including long-range transport of pollution from continental Europe. A quadrupole aerosol mass spectrometer (Q-AMS) was employed to measure the size-resolved chemical composition of non-refractory submicron aerosol (NR-PM1), and to estimate the extent of oxidation of the organic aerosol. Factor analysis was used to gain insights into the processes and sources affecting the OA composition. The particles were internally mixed and liquid. The largest fraction of the dry NR-PM1 sampled was ammonium sulfate and ammonium bisulfate, followed by organics and a small amount of nitrate. The variability in OA composition could be explained with two factors of oxygenated organic aerosol (OOA) with differing extents of oxidation but similar volatility. Hydrocarbon-like organic aerosol (HOA) was not detected. There was no statistically significant diurnal variation in the bulk composition of NR-PM1 such as total sulfate or total organic aerosol concentrations. However, the OA composition exhibited statistically significant diurnal variation with more oxidized OA in the afternoon. The organic aerosol was highly oxidized, regardless of the source region. Total OA concentrations also varied little with time of day, suggesting that local sources had only a small effect on OA concentrations measured at Finokalia. The aerosol was transported for about one day before arriving at the site, corresponding to an OH exposure of approximately 4×1011 molecules cm-3 s. The constant extent of oxidation suggests that atmospheric aging results in a highly oxidized OA at these OH exposures, regardless of the aerosol source.

  10. Aged organic aerosol in the Eastern Mediterranean: the Finokalia Aerosol Measurement Experiment - 2008

    NASA Astrophysics Data System (ADS)

    Hildebrandt, L.; Engelhart, G. J.; Mohr, C.; Kostenidou, E.; Lanz, V. A.; Bougiatioti, A.; Decarlo, P. F.; Prevot, A. S. H.; Baltensperger, U.; Mihalopoulos, N.; Donahue, N. M.; Pandis, S. N.

    2010-05-01

    Aged organic aerosol (OA) was measured at a remote coastal site on the island of Crete, Greece during the Finokalia Aerosol Measurement Experiment-2008 (FAME-2008), which was part of the EUCAARI intensive campaign of May 2008. The site at Finokalia is influenced by air masses from different source regions, including long-range transport of pollution from continental Europe. A quadrupole aerosol mass spectrometer (Q-AMS) was employed to measure the size-resolved chemical composition of non-refractory submicron aerosol (NR-PM1), and to estimate the extent of oxidation of the organic aerosol. Factor analysis was used to gain insights into the processes and sources affecting the OA composition. The particles were internally mixed and liquid. The largest fraction of the dry NR-PM1 sampled was ammonium sulfate and ammonium bisulfate, followed by organics and a small amount of nitrate. The variability in OA composition could be explained with two factors of oxygenated organic aerosol (OOA) with differing extents of oxidation but similar volatility. Hydrocarbon-like organic aerosol (HOA) was not detected. There was no statistically significant diurnal variation in the bulk composition of NR-PM1 such as total sulfate or total organic aerosol concentrations. However, the OA composition exhibited statistically significant diurnal variation with more oxidized OA in the afternoon. The organic aerosol was highly oxidized, regardless of the source region. Total OA concentrations also varied little with source region, suggesting that local sources had only a small effect on OA concentrations measured at Finokalia. The aerosol was transported for about one day before arriving at the site, corresponding to an OH exposure of approximately 4×1011 molecules cm-3 s. The constant extent of oxidation suggests that atmospheric aging results in a highly oxidized OA at these OH exposures, regardless of the aerosol source.

  11. Molecular Characterization of Nitrogen Containing Organic Compounds in Biomass Burning Aerosols Using High Resolution Mass Spectrometry

    SciTech Connect

    Laskin, Alexander; Smith, Jeffrey S.; Laskin, Julia

    2009-05-13

    Although nitrogen-containing organic compounds (NOC) are important components of atmospheric aerosols, little is known about their chemical compositions. Here we present detailed characterization of the NOC constituents of biomass burning aerosol (BBA) samples using high resolution electrospray ionization mass spectrometry (ESI/MS). Accurate mass measurements combined with MS/MS fragmentation experiments of selected ions were used to assign molecular structures to individual NOC species. Our results indicate that N-heterocyclic alkaloid compounds - species naturally produced by plants and living organisms - comprise a substantial fraction of NOC in BBA samples collected from test burns of five biomass fuels. High abundance of alkaloids in test burns of ponderosa pine - a widespread tree in the western U.S. areas frequently affected by large scale fires - suggests that N-heterocyclic alkaloids in BBA can play a significant role in dry and wet deposition of fixed nitrogen in this region.

  12. MELCOR 1.8.2 assessment: Aerosol experiments ABCOVE AB5, AB6, AB7, and LACE LA2

    SciTech Connect

    Souto, F.J.; Haskin, F.E.; Kmetyk, L.N.

    1994-10-01

    The MELCOR computer code has been used to model four of the large-scale aerosol behavior experiments conducted in the Containment System Test Facility (CSTF) vessel. Tests AB5, AB6 and AB7 of the ABCOVE program simulate the dry aerosol conditions during a hypothetical severe accident in an LMFBR. Test LA2 of the LACE program simulates aerosol behavior in a condensing steam environment during a postulated severe accident in an LWR with failure to isolate the containment. The comparison of code results to experimental data show that MELCOR is able to correctly predict most of the thermal-hydraulic results in the four tests. MELCOR predicts reasonably well the dry aerosol behavior of the ABCOVE tests, but significant disagreements are found in the aerosol behavior modelling for the LA2 experiment. These results tend to support some of the concerns about the MELCOR modelling of steam condensation onto aerosols expressed in previous works. During these analyses, a limitation in the MELCOR input was detected for the specification of the aerosol parameters for more than one component. A Latin Hypercube Sampling (LHS) sensitivity study of the aerosol dynamic constants is presented for test AB6. The study shows the importance of the aerosol shape factors in the aerosol deposition behavior, and reveals that MELCOR input/output processing is highly labor intensive for uncertainty and sensitivity analyses based on LHS.

  13. Ganges Valley Aerosol Experiment (GVAX) Final Campaign Report

    SciTech Connect

    Kotamarthi, VR

    2013-12-01

    In general, the Indian Summer Monsoon (ISM) as well as the and the tropical monsoon climate is influenced by a wide range of factors. Under various climate change scenarios, temperatures over land and into the mid troposphere are expected to increase, intensifying the summer pressure gradient differential between land and ocean and thus strengthening the ISM. However, increasing aerosol concentration, air pollution, and deforestation result in changes to surface albedo and insolation, potentially leading to low monsoon rainfall. Clear evidence points to increasing aerosol concentrations over the Indian subcontinent with time, and several hypotheses regarding the effect on monsoons have been offered. The Ganges Valley Aerosol Experiment (GVAX) field study aimed to provide critical data to address these hypotheses and contribute to developing better parameterizations for tropical clouds, convection, and aerosol-cloud interactions. The primary science questions for the mission were as follows:

  14. Discrete dipole approximation for black carbon-containing aerosols in arbitrary mixing state: A hybrid discretization scheme

    NASA Astrophysics Data System (ADS)

    Moteki, Nobuhiro

    2016-07-01

    An accurate and efficient simulation of light scattering by an atmospheric black carbon (BC)-containing aerosol-a fractal-like cluster of hundreds of carbon monomers that is internally mixed with other aerosol compounds such as sulfates, organics, and water-remains challenging owing to the enormous diversities of such aerosols' size, shape, and mixing state. Although the discrete dipole approximation (DDA) is theoretically an exact numerical method that is applicable to arbitrary non-spherical inhomogeneous targets, in practice, it suffers from severe granularity-induced error and degradation of computational efficiency for such extremely complex targets. To solve this drawback, we propose herein a hybrid DDA method designed for arbitrary BC-containing aerosols: the monomer-dipole assumption is applied to a cluster of carbon monomers, whereas the efficient cubic-lattice discretization is applied to the remaining particle volume consisting of other materials. The hybrid DDA is free from the error induced by the surface granularity of carbon monomers that occurs in conventional cubic-lattice DDA. In the hybrid DDA, we successfully mitigate the artifact of neglecting the higher-order multipoles in the monomer-dipole assumption by incorporating the magnetic dipole in addition to the electric dipole into our DDA formulations. Our numerical experiments show that the hybrid DDA method is an efficient light-scattering solver for BC-containing aerosols in arbitrary mixing states. The hybrid DDA could be also useful for a cluster of metallic nanospheres associated with other dielectric materials.

  15. Aerosol effect on Umkehr ozone profiles using Stratospheric Aerosol and Gas Experiment II measurements

    NASA Technical Reports Server (NTRS)

    Newchurch, M. J.; Cunnold, D. M.

    1994-01-01

    This study examines 1211 cases of coincident ozone profiles derived from 1164 Umkehrs and 928 Stratospheric Aerosol and Gas Experiment II (SAGE II) profiles within 1000 km and 12 hours between October 1984 and April 1989 to study the stratospheric-aerosol effect on Umkehr ozone profiles. Because of the close correspondence of stratospheric aerosol optical depth at the SAGE II-measured 0.525-micrometer wavelength and the extrapolated 0.32 Umkehr wavelength determined in this study we use the 0.525-micrometer data to determine the aerosol effect on Umkehr profiles. At the 95% confidence level, we find the following errors to the Umkehr ozone amounts: in Umkehr layer 9 (-2.9 +/- 2.1), layer 8 (-2.3 +/- 1.1), layer 7 (0.1 +/- 1.1), layer 6 (2.2 +/- 1.0), layer 5 (-1.5 +/- 0.8), and layer 4 (-2.4 +/- 1.7) in percent ozone amount per 0.01 stratospheric aerosol optical depth. These results agree with previous theoretical and empirical studies within their respective error bounds in layers 9, 8, and 7. The results in layers 6, 5, and 4 differ significantly from those in previous works. Using only those eight stations with more than 47 coincidences results in mean aerosol effects that are not significantly different from the 14-station results. Because SAGE II and Umkehr produce different ozone retrievals in layer 9 and because the intralayer correlation of SAGE II ozone and aerosol in layer 9 is nonzero, one must exercise some caution in attributing the entire SAGE II-Umkehr difference in this layer to an aerosol effect.

  16. Evaluation of cell sorting aerosols and containment by an optical airborne particle counter.

    PubMed

    Xie, Mike; Waring, Michael T

    2015-08-01

    Understanding aerosols produced by cell sorting is critical to biosafety risk assessment and validation of containment efficiency. In this study an Optical Airborne Particle Counter was used to analyze aerosols produced by the BD FACSAria and to assess the effectiveness of its aerosol containment. The suitability of using this device to validate containment was directly compared to the Glo-Germ method put forth by the International Society for Advancement of Cytometry (ISAC) as a standard for testing. It was found that high concentrations of aerosols ranging from 0.3 µm to 10 µm can be detected in failure mode, with most less than 5 µm. In most cases, while numerous aerosols smaller than 5 µm were detected by the Optical Airborne Particle Counter, no Glo-Germ particles were detected, indicating that small aerosols are under-evaluated by the Glo-Germ method. The results demonstrate that the Optical Airborne Particle Counter offers a rapid, economic, and quantitative analysis of cell sorter aerosols and represents an improved method over Glo-Germ for the task of routine validation and monitoring of aerosol containment for cell sorting. PMID:26012776

  17. 10 CFR 32.26 - Gas and aerosol detectors containing byproduct material: Requirements for license to manufacture...

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 10 Energy 1 2010-01-01 2010-01-01 false Gas and aerosol detectors containing byproduct material... CONTAINING BYPRODUCT MATERIAL Exempt Concentrations and Items § 32.26 Gas and aerosol detectors containing... application for a specific license to manufacture, process, or produce gas and aerosol detectors...

  18. Containment Prospectus for the TRUMPET Experiments

    SciTech Connect

    Pawloski, G A

    2004-02-05

    TRUMPET is a series of dynamic subcritical experiments planned for execution in the U1a.102D alcove of the U1a Complex at the Nevada Test Site (NTS). The location of LLNL drifts at the U1a Complex is shown in Figure 1. The data from the TRUMPET experiments will be used in the Stockpile Stewardship Program to assess the aging of nuclear weapons components and to better model the long-term performance of weapons in the enduring stockpile. The TRUMPET series of experiments will be conducted in an almost identical way as the OBOE series of experiments. Individual TRUMPET experiments will be housed in an experiment vessel, as was done for OBOE. These vessels are the same as those utilized for OBOE. All TRUMPET experiments will occur in the zero room in the U1a.102D alcove, which is on the opposite side of the U1a.102 drift from U1a.102C, which housed the OBOE experiments. The centerlines of these two alcoves are separated by only 10 feet. As with OBOE experiments, expended TRUMPET experiment vessels will be moved to the back of the alcove and entombed in grout. After the TRUMPET series of experiments is completed, another experiment will be sited in the U1a.102D alcove and it will be the final experiment in the zero room, as was similarly done for the OBOE series of experiments followed by the execution of the PIANO experiment. Each experimental package for TRUMPET will be composed of high explosive (HE) and special nuclear material (SNM) in a subcritical assembly. Each experimental package will be placed in an experimental vessel within the TRUMPET zero room in the U1a.102D alcove. The containment plan for the TRUMPET experiments utilizes a two-nested containment vessel concept, similar to OBOE and other subcritical experiments in the U1a Complex. The first containment vessel is formed by the primary containment barrier that seals the U1a.102D drift. The second containment vessel is formed by the secondary containment barrier in the U1a.100 drift. While it is likely

  19. The Finokalia Aerosol Measurement Experiment - 2008 (FAME-08): an overview

    NASA Astrophysics Data System (ADS)

    Pikridas, M.; Bougiatioti, A.; Hildebrandt, L.; Engelhart, G. J.; Kostenidou, E.; Mohr, C.; Prévôt, A. S. H.; Kouvarakis, G.; Zarmpas, P.; Burkhart, J. F.; Lee, B.-H.; Psichoudaki, M.; Mihalopoulos, N.; Pilinis, C.; Stohl, A.; Baltensperger, U.; Kulmala, M.; Pandis, S. N.

    2010-07-01

    A month (4 May to 8 June 2008) of ambient aerosol, air ion and gas phase sampling (Finokalia Aerosol Measurement Experiment 2008, FAME-08) was conducted at Finokalia, on the island of Crete, Greece. The purpose of the study was to characterize the physical and chemical properties of aged aerosol and to investigate new particle formation. Measurements included aerosol and air ion size distributions, size-resolved chemical composition, organic aerosol thermal volatility, water uptake and particle optical properties (light scattering and absorption). Statistical analysis of the aerosol mass concentration variations revealed the absence of diurnal patterns suggesting the lack of strong local sources. Sulfates accounted for approximately half of the particulate matter less than 1 micrometer in diameter (PM1) and organics for 28%. The PM1 organic aerosol fraction was highly oxidized with 80% water soluble. The supermicrometer particles were dominated by crustal components (50%), sea salt (24%) and nitrates (16%). The organic carbon to elemental carbon (OC/EC) ratio correlated with ozone measurements but with a one-day lag. The average OC/EC ratio for the study period was equal to 5.4. For three days air masses from North Africa resulted in a 6-fold increase of particulate matter less than 10 micrometers in diameter (PM10) and a decrease of the OC/EC ratio by a factor of 2. Back trajectory analysis, based on FLEXPART footprint plots, identified five source regions (Athens, Greece, Africa, other continental and marine), each of which influenced the PM1 aerosol composition and properties. Marine air masses had the lowest PM1 concentrations and air masses from the Balkans, Turkey and Eastern Europe the highest.

  20. The Finokalia Aerosol Measurement Experiment - 2008 (FAME-08): an overview

    NASA Astrophysics Data System (ADS)

    Pikridas, M.; Bougiatioti, A.; Hildebrandt, L.; Engelhart, G. J.; Kostenidou, E.; Mohr, C.; Prevot, A. S. H.; Kouvarakis, G.; Zarmpas, P.; Burkhart, J. F.; Lee, B.-H.; Psichoudaki, M.; Mihalopoulos, N.; Pilinis, C.; Stohl, A.; Baltensperger, U.; Kulmala, M.; Pandis, S. N.

    2010-03-01

    A month (4 May to 8 June 2008) of ambient aerosol, air ion and gas phase sampling (Finokalia Aerosol Measurement Experiment 2008, FAME-08) was conducted at Finokalia, on the island of Crete, Greece. The purpose of the study was to characterize the physical and chemical properties of aged aerosol and to investigate new particle formation. Measurements included aerosol and air ion size distributions, size-resolved chemical composition, organic aerosol thermal volatility, water uptake and particle optical properties (light scattering and absorption). Statistical analysis of the aerosol mass concentration variations revealed the absence of diurnal patterns suggesting the lack of strong local sources. Sulfates accounted for approximately half of the particulate matter less than 1 micrometer in diameter (PM1) and organics for 26%. The PM1 organic aerosol fraction was highly oxidized with 80% water soluble. The supermicrometer particles were dominated by crustal components (50%), sea salt (24%) and nitrates (16%). The organic carbon to elemental carbon (OC/EC) ratio correlated with ozone measurements but with a one-day lag. The average OC/EC ratio for the study period was equal to 5.4. For three days air masses from North Africa resulted in a 6-fold increase of particulate matter less than 10 micrometers in diameter (PM10) and a decrease of the OC/EC ratio by a factor of 2. Back trajectory analysis, based on FLEXPART footprint plots, identified five source regions (Athens, Greece, Africa, other continental and marine), each of which influenced the PM1 aerosol composition and properties. Marine air masses had the lowest PM1 concentrations and air masses from the Balkans, Turkey and Eastern Europe the highest.

  1. Containment Prospectus for the PIANO Experiment

    SciTech Connect

    Burkhard, N R

    2001-03-23

    PIANO is a dynamic, subcritical, zero-yield experiment intended for execution in the U1a.102C drift of the U1a complex at the Nevada Test Site (NTS) (Figure 1). The data from the PIANO experiment will be used in the Stockpile Stewardship Program to assess the aging of nuclear weapon components and to better model the long-term performance of the weapons in the enduring stockpile. The PIANO experiment is composed of one experimental package. The experimental package will have high explosive (HE) and special nuclear material (SNM) in a subcritical assembly. The containment plan for the PIANO series of experiments utilizes a two-containment-vessel concept. The first Containment vessel is formed by the primary containment barrier that seals the U1a.102C drift. The second containment vessel is formed by the secondary containment barrier in the U100 drift. The PIANO experiment is the final experiment to be conducted in the U1a.102C alcove. It will be an ''open'' experiment--meaning that PIANO will not utilize a confinement vessel as the previous OBOE experiments in this alcove did. We expect that the SNM from the PIANO experiment will be fully contained within the first containment vessel.

  2. Elemental composition of aerosols in fourteen experiments of the Cloud Condensation Nuclei Workshop

    NASA Technical Reports Server (NTRS)

    Mach, W. H.; Hucek, R. R.

    1981-01-01

    Aeosols were collected with two Ci impactors and analyzed with proton induced X-ray emission (PIXE) for chemical composition and to detect if contamination was present. One of the impactors sampled the generated aerosols; the other impactor sampled droplets from a diffusion cloud chamber. The purpose of the experiments was to test the feasibility of a study of the transfer of chemical elements from the fine particle sizes to the coarse particle sizes, after CCN are activated and cloud droplets are formed. The data indicated that sulfur-containing aerosols did exhibit the expected transfer.

  3. Ganges Valley Aerosol Experiment: Science and Operations Plan

    SciTech Connect

    Kotamarthi, VR

    2010-06-21

    The Ganges Valley region is one of the largest and most rapidly developing sections of the Indian subcontinent. The Ganges River, which provides the region with water needed for sustaining life, is fed primarily by snow and rainfall associated with Indian summer monsoons. Impacts of changes in precipitation patterns, temperature, and the flow of the snow-fed rivers can be immense. Recent satellite-based measurements have indicated that the upper Ganges Valley has some of the highest persistently observed aerosol optical depth values. The aerosol layer covers a vast region, extending across the Indo-Gangetic Plain to the Bay of Bengal during the winter and early spring of each year. The persistent winter fog in the region is already a cause of much concern, and several studies have been proposed to understand the economic, scientific, and societal dimensions of this problem. During the INDian Ocean EXperiment (INDOEX) field studies, aerosols from this region were shown to affect cloud formation and monsoon activity over the Indian Ocean. This is one of the few regions showing a trend toward increasing surface dimming and enhanced mid-tropospheric warming. Increasing air pollution over this region could modify the radiative balance through direct, indirect, and semi-indirect effects associated with aerosols. The consequences of aerosols and associated pollution for surface insolation over the Ganges Valley and monsoons, in particular, are not well understood. The proposed field study is designed for use of (1) the ARM Mobile Facility (AMF) to measure relevant radiative, cloud, convection, and aerosol optical characteristics over mainland India during an extended period of 9–12 months and (2) the G-1 aircraft and surface sites to measure relevant aerosol chemical, physical, and optical characteristics in the Ganges Valley during a period of 6–12 weeks. The aerosols in this region have complex sources, including burning of coal, biomass, and biofuels; automobile

  4. The Indian ocean experiment: aerosol forcing obtained from satellite data

    NASA Astrophysics Data System (ADS)

    Rajeev, K.; Ramanathan, V.

    The tropical Indian Ocean provides an ideal and unique natural laboratory to observe and understand the role of anthropogenic aerosols in climate forcing. Since 1996, an international team of American, European and Indian scientists have been collecting aerosol, chemical and radiation data from ships and surface stations, which culminated in a multi-platform field experiment conducted during January to March of 1999. A persistent haze layer that spread over most of the northern Indian Ocean during wintertime was discovered. The layer, a complex mix of organics, black carbon, sulfates, nitrates and other species, subjects the lower atmosphere to a strong radiative heating and a larger reduction in the solar heating of the ocean. We present here the regional distribution of aerosols and the resulting clear sky aerosol radiative forcing at top-of-atmosphere (TOA) observed over the Indian Ocean during the winter months of 1997, 1998 and 1999 based on the aerosol optical depth (AOD) estimated using NOAA14-AVHRR and the TOA radiation budget data from CERES on board TRMM. Using the ratio of surface to TOA clear sky aerosol radiative forcing observed during the same period over the Indian Ocean island of Kaashidhoo (Satheesh and Ramanathan, 2000), the clear sky aerosol radiative forcing at the surface and the atmosphere are discussed. The regional maps of AVHRR derived AOD show abnormally large aerosol concentration during the winter of 1999 which is about 1.5 to 2 times larger than the AOD during the corresponding period of 1997 and 1998. A large latitudinal gradient in AOD is observed during all the three years of observation, with maximum AOD in the northern hemisphere. The diurnal mean clear sky aerosol forcing at TOA in the northern hemisphere Indian Ocean is in the range of -4 to -16 Wm -2 and had large spatio-temporal variations while in the southern hemisphere Indian Ocean it is in the range of 0 to -6Wm -2. The importance of integrating in-situ data with satellite

  5. Prenatal Experiences of Containment in the Light of Bion's Model of Container/Contained

    ERIC Educational Resources Information Center

    Maiello, Suzanne

    2012-01-01

    This paper explores the idea of possible proto-experiences of the prenatal child in the context of Bion's model of container/contained. The physical configuration of the embryo/foetus contained in the maternal uterus represents the starting point for an enquiry into the unborn child's possible experiences of its state of being contained in a…

  6. Aerosol Climate Effects: Local Radiative Forcing and Column Closure Experiments

    NASA Technical Reports Server (NTRS)

    Russell, P. B.; Bergstrom, Robert W.; Kinne, S. A.

    2000-01-01

    In an effort to reduce uncertainties in climate change predictions, experiments are being planned and conducted to measure anthropogenic aerosol properties and effects, including effects on radiative fields. The global average, direct anthropogenic aerosol effect on upwelling shortwave fluxes is estimated to be about +1/2 W/sq m, whereas errors in flux changes measured with airborne and spaceborne radiometers are 2 to 8 W/sq m or larger. This poses the question of whether flux changes expected in field experiments will be large enough to measure accurately. This paper obtains a new expression for the aerosol-induced change in upwelling flux, compares it to two-stream and adding-doubling (AD) results, and uses all three methods to estimate expected flux changes. The new expression accounts for the solar zenith angle dependences of aerosol transmission and reflection, as well as of surface albedo, all of which can have a strong effect in determining flux changes measured in field experiments. Despite its relative simplicity, the new expression gives results similar to previous two-stream results. Relative to AD results, it agrees within a few watts per square meter for the intermediate solar elevation angles where the flux changes peak (roughly 10 to 30 degrees), but it has negative errors for higher Sun and positive errors for lower Sun. All three techniques yield aerosol-induced changes in upwelling flux of +8 to +50 W/sq m for aerosol midvisible optical depths of 0.1 to 0.5. Because such aerosol optical depths occur frequently off the U.S. and European Atlantic coasts in summer, the flux changes they induce should be measurable by airborne, and possibly by spaceborne, radiometers, provided sufficient care is taken in experiment design (including measurements to separate aerosol radiative effects from those of absorbing gases). The expected flux changes are about 15 to 100 times larger than the global average flux change expected for the global average

  7. Continuation of Lithium Aerosol Injection Experiments on NSTX

    NASA Astrophysics Data System (ADS)

    Mansfield, D. K.; Roquemore, A. L.; Kugel, H.; Maingi, R.; Irby, J.; Wang, Z.

    2009-11-01

    During the 2008 run campaign, a Li powder dropper was installed on NSTX that successfully injected up to 35 mg/s of Li aerosol into the SOL. Initial improvements in the plasma performance from these initial experiments warranted the installation of a second Li dropper for the 2009 campaign. Design improvements in the dropper have resulted in accurate control of the flux of Li powder injected. The improved duel-dropper system has injected lithium fluxes of from 30 - 140 mg/s. At the highest flux, plasmas of 950 kA with 6 MW off NBI auxiliary heating have been successfully operated. This flux corresponds to 2.5 x106 - 5.8 x106 aerosol particles/s and is stoichiometrically equivalent 80 - 187 Torr L/s of D2. Operation of the Li dropper and the effects of the Li aerosol on the plasma performance will be discussed.

  8. Complex Aerosol Experiment in Western Siberia (April - October 2013)

    NASA Astrophysics Data System (ADS)

    Matvienko, G. G.; Belan, B. D.; Panchenko, M. V.; Romanovskii, O. A.; Sakerin, S. M.; Kabanov, D. M.; Turchinovich, S. A.; Turchinovich, Yu. S.; Eremina, T. A.; Kozlov, V. S.; Terpugova, S. A.; Pol'kin, V. V.; Yausheva, E. P.; Chernov, D. G.; Zuravleva, T. B.; Bedareva, T. V.; Odintsov, S. L.; Burlakov, V. D.; Arshinov, M. Yu.; Ivlev, G. A.; Savkin, D. E.; Fofonov, A. V.; Gladkikh, V. A.; Kamardin, A. P.; Balin, Yu. S.; Kokhanenko, G. P.; Penner, I. E.; Samoilova, S. V.; Antokhin, P. N.; Arshinova, V. G.; Davydov, D. K.; Kozlov, A. V.; Pestunov, D. A.; Rasskazchikova, T. M.; Simonenkov, D. V.; Sklyadneva, T. K.; Tolmachev, G. N.; Belan, S. B.; Shmargunov, V. P.

    2016-06-01

    The primary project objective was to accomplish the Complex Aerosol Experiment, during which the aerosol properties should be measured in the near-ground layer and free atmosphere. Three measurement cycles were performed during the project implementation: in spring period (April), when the maximum of aerosol generation is observed; in summer (July), when atmospheric boundary layer height and mixing layer height are maximal; and in late summer - early autumn (October), when the secondary particle nucleation period is recorded. Numerical calculations were compared with measurements of fluxes of downward solar radiation. It was shown that the relative differences between model and experimental values of fluxes of direct and total radiation, on the average, do not exceed 1% and 3% respectively.

  9. Skylab experiment performance evaluation manual. Appendix P: Experiment T003 inflight aerosol analysis (DOT/MSFC)

    NASA Technical Reports Server (NTRS)

    Purushotham, K. S.

    1972-01-01

    A series of analyses is presented for experiment T003, inflight aerosol analysis, to be used for evaluating the performance of the Skylab corollary experiments under preflight, inflight, and post-flight conditions. Experiment contingency plan workaround procedure and malfunction analyses are presented in order to assist in making the experiment operationally successful.

  10. Analysis of Nitrogen Containing Organic Compounds in Biomass Burning Aerosols Using High Resolution Mass Spectrometry

    NASA Astrophysics Data System (ADS)

    Laskin, A.; Smith, J. S.; Laskin, J.

    2009-05-01

    Chemical characterization of atmospheric aerosols presents a serious analytical challenge because of the complexity of particulate matter analyte composed of a large number of compounds with a wide range of molecular structures, physico-chemical properties, and reactivity. In this study the chemical composition of the nitrogen containing organic (NOC) constituents of biomass burning aerosol (BBA) samples is characterized by high-resolution electrospray ionization mass spectrometry (ESI/MS). Accurate mass measurements combined with MS/MS fragmentation experiments of selected ions were used to assign molecular structures to individual NOC species. Our results indicate that N-heterocyclic alkaloid compounds - species naturally produced by plants and living organisms - comprise a substantial fraction of NOC in BBA samples collected from test burns of five biomass fuels. High abundance of alkaloids in test burns of ponderosa pine - a widespread tree in the western U.S. areas frequently affected by large scale fires - suggests that N-heterocyclic alkaloids in BBA may play a significant role in dry and wet deposition of fixed nitrogen in this region. Atmospheric processing and chemical transformations of alkaloids in the particulate phase will be discussed.

  11. A simplified model of aerosol removal by natural processes in reactor containments

    SciTech Connect

    Powers, D.A.; Washington, K.E.; Sprung, J.L.; Burson, S.B.

    1996-07-01

    Simplified formulae are developed for estimating the aerosol decontamination that can be achieved by natural processes in the containments of pressurized water reactors and in the drywells of boiling water reactors under severe accident conditions. These simplified formulae were derived by correlation of results of Monte Carlo uncertainty analyses of detailed models of aerosol behavior under accident conditions. Monte Carlo uncertainty analyses of decontamination by natural aerosol processes are reported for 1,000, 2,000, 3,000, and 4,000 MW(th) pressurized water reactors and for 1,500, 2,500, and 3,500 MW(th) boiling water reactors. Uncertainty distributions for the decontamination factors and decontamination coefficients as functions of time were developed in the Monte Carlo analyses by considering uncertainties in aerosol processes, material properties, reactor geometry and severe accident progression. Phenomenological uncertainties examined in this work included uncertainties in aerosol coagulation by gravitational collision, Brownian diffusion, turbulent diffusion and turbulent inertia. Uncertainties in aerosol deposition by gravitational settling, thermophoresis, diffusiophoresis, and turbulent diffusion were examined. Electrostatic charging of aerosol particles in severe accidents is discussed. Such charging could affect both the coagulation and deposition of aerosol particles. Electrostatic effects are not considered in most available models of aerosol behavior during severe accidents and cause uncertainties in predicted natural decontamination processes that could not be taken in to account in this work. Median (50%), 90 and 10% values of the uncertainty distributions for effective decontamination coefficients were correlated with time and reactor thermal power. These correlations constitute a simplified model that can be used to estimate the decontamination by natural aerosol processes at 3 levels of conservatism. Applications of the model are described.

  12. Preliminary Results from the Smoke Aerosol Measurement Experiment - Reflight

    NASA Astrophysics Data System (ADS)

    Urban, D. L.; Ruff, G. A.; Mulholland, G. W.; Yuan, Z.; Cleary, T.; Yang, J.; Meyer, M. E.; Bryg, V. M.

    2012-01-01

    Preliminary results are presented from the Reflight of the Smoke Aerosol Measurement Experiment (SAME- R) which was conducted during Expedition 24 (July- September 2010). The reflight experiment built upon the results of the original flight during Expedition 15 by adding diagnostic measurements and expanding the test matrix. Five different materials representative of those found in spacecraft (Teflon, Kapton, cotton, silicone rubber and Pyrell) were heated to temperatures below the ignition point with conditions controlled to provide repeatable sample surface temperatures and air flow. Particle size determinations were made using aerosol instruments and by capturing particles for ground based examination in a Transmission Electron Microscope (TEM). Overall the majority of the average smoke particle sizes were found to be in the 200 to 400 nanometer range with the some of the quiescent cases producing substantially larger particles. When combined with particle morphology data from the TEM analysis, these results can be used to guide the design of future smoke detectors.

  13. Rural continental aerosol properties and processes observed during the Hohenpeissenberg Aerosol Characterization Experiment (HAZE2002)

    NASA Astrophysics Data System (ADS)

    Hock, N.; Schneider, J.; Borrmann, S.; Römpp, A.; Moortgat, G.; Franze, T.; Schauer, C.; Pöschl, U.; Plass-Dülmer, C.; Berresheim, H.

    2007-06-01

    Detailed investigations of the chemical and microphysical properties of rural continental aerosols were performed during the HAZE2002 experiment, which was conducted in May 2002 at the Meteorological Observatory Hohenpeissenberg (DWD) in Southern Germany. The online measurement data and techniques included: size-resolved chemical composition of submicron particles by aerosol mass spectrometry (AMS); total particle number concentrations and size distributions over the diameter range of 3 nm to 9 μm (CPC, SMPS, OPC); monoterpenes determined by gas chromatography- ion trap mass spectrometry; OH and H2SO4 determined by atmospheric pressure chemical ionization mass spectrometry (CIMS). Filter sampling and offline analytical techniques were used to determine: fine particle mass (PM2.5), organic, elemental and total carbon in PM2.5 (OC2.5, EC2.5, TC2.5), and selected organic compounds (dicarboxylic acids, polycyclic aromatic hydrocarbons, proteins). Overall, the non-refractory components of submicron particles detected by aerosol mass spectrometry (PM1, 6.6±5.4 μg m-3, arithmetic mean and standard deviation) accounted for ~62% of PM2.5 determined by filter gravimetry (10.6±4.7 μg m-3). The relative proportions of non-refractory submicron particle components were: 11% ammonium, 19% nitrate, 20% sulfate, and 50% organics (OM1). In spite of strongly changing meteorological conditions and absolute concentration levels of particulate matter (3-13 μg m-3 PM1), OM1 was closely correlated with PM1 (r2=0.9) indicating a near-constant ratio of non-refractory organics and inorganics. In contrast, the ratio of nitrate to sulfate was highly dependent on temperature (14-32°C) and relative humidity (20-100%), which could be explained by thermodynamic model calculations of NH3/HNO3/NH4NO3 gas-particle partitioning. From the combination of optical and other sizing techniques (OPC, AMS, SMPS), an average refractive index of 1.40-1.45 was inferred for the measured rural aerosol

  14. Comparison of two in vitro systems to assess cellular effects of nanoparticles-containing aerosols

    PubMed Central

    Fröhlich, Eleonore; Bonstingl, Gudrun; Höfler, Anita; Meindl, Claudia; Leitinger, Gerd; Pieber, Thomas R.; Roblegg, Eva

    2013-01-01

    Inhalation treatment with nanoparticle containing aerosols appears a promising new therapeutic option but new formulations have to be assessed for efficacy and toxicity. We evaluated the utility of a VITROCELL®6 PT-CF + PARI LC SPRINT® Baby Nebulizer (PARI BOY) system compared with a conventional MicroSprayer. A549 cells were cultured in the air–liquid interface, exposed to nanoparticle aerosols and characterized by measurement of transepithelial electrical resistance and staining for tight junction proteins. Deposition and distribution rates of polystyrene particles and of carbon nanotubes on the cells were assessed. In addition, cytotoxicity of aerosols containing polystyrene particles was compared with cytotoxicity of polystyrene particles in suspension tested in submersed cultures. Exposure by itself in both exposure systems did not damage the cells. Deposition rates of aerosolized polystyrene particles were about 700 times and that of carbon nanotubes about 4 times higher in the MicroSprayer than in the VITROCELL®6 PT-CF system. Cytotoxicity of amine-functionalized polystyrene nanoparticles was significantly higher when applied as an aerosol on cell cultured in air–liquid interface culture compared with nanoparticle suspensions tested in submersed culture. The higher cytotoxicity of aerosolized nanoparticles underscores the importance of relevant exposure systems. PMID:22906573

  15. The influence of fog parameters on aerosol depletion measured in the KAEVER experiments

    SciTech Connect

    Poss, G.; Weber, D.; Fritsche, B.

    1995-12-31

    The release of radioactive aerosols in the environment is one of the most serious hazards in case of an accident in nuclear power plant. Many efforts have been made in the past in numerous experimental programs like NSPP, DEMONA, VANAM, LACE, MARVIKEN, others are still underway to improve the knowledge of the aerosol behavior and depletion in a reactor containment in order to estimate the possible source term and to validate computer codes. In the German single compartment KAEVER facility the influence of size distribution, morphology, composition and solubility on the aerosol behavior is investigated. One of the more specific items is to learn about {open_quotes}wet depletion{close_quotes} means, the aerosol depletion behavior in condensing atmospheres. There are no experiments known where the fog parameters like droplet size distribution, volume concentration, respectively airborne liquid water content have been measured in- and on-line explicitly. To the authors knowledge the use of the Battelle FASP photometer, which was developed especially for this reason, for the first time gives insight in condensation behavior under accident typical thermal hydraulic conditions. It delivers a basis for code validation in terms of a real comparison of measurements and calculations. The paper presents results from {open_quotes}wet depletion{close_quotes} aerosol experiments demonstrating how depletion velocity depends on the fog parameters and where obviously critical fog parameter seem to change the regime from a {open_quotes}pseudo dry depletion{close_quotes} at a relative humidity of 100% but quasi no or very low airborne liquid water content to a real {open_quotes}wet depletion{close_quotes} under the presence of fogs with varying densities. Characteristics are outlined how soluble and insoluble particles as well as aerosol mixtures behave under condensing conditions.

  16. Results from the DCH-1 (Direct Containment Heating) experiment. [Pressurized melt ejection and direct containment heating

    SciTech Connect

    Tarbell, W.W.; Brockmann, J.E.; Pilch, M.; Ross, J.E.; Oliver, M.S.; Lucero, D.A.; Kerley, T.E.; Arellano, F.E.; Gomez, R.D.

    1987-05-01

    The DCH-1 (Direct Containment Heating) test was the first experiment performed in the Surtsey Direct Heating Test Facility. The test involved 20 kg of molten core debris simulant ejected into a 1:10 scale model of the Zion reactor cavity. The melt was produced by a metallothermic reaction of iron oxide and aluminum powders to yield molten iron and alumina. The cavity model was placed so that the emerging debris propagated directly upwards along the vertical centerline of the chamber. Results from the experiment showed that the molten material was ejected from the caviity as a cloud of particles and aerosol. The dispersed debris caused a rapid pressurization of the 103-m/sup 3/ chamber atmosphere. Peak pressure from the six transducers ranged from 0.09 to 0.13 MPa (13.4 to 19.4 psig) above the initial value in the chamber. Posttest debris collection yielded 11.6 kg of material outside the cavity, of which approximately 1.6 kg was attributed to the uptake of oxygen by the iron particles. Mechanical sieving of the recovered debris showed a lognormal size distribution with a mass mean size of 0.55 mm. Aerosol measurements indicated a subsantial portion (2 to 16%) of the ejected mass was in the size range less than 10 m aerodynamic equivalent diameter.

  17. Rural continental aerosol properties and processes observed during the Hohenpeissenberg Aerosol Characterization Experiment (HAZE2002)

    NASA Astrophysics Data System (ADS)

    Hock, N.; Schneider, J.; Borrmann, S.; Römpp, A.; Moortgat, G.; Franze, T.; Schauer, C.; Pöschl, U.; Plass-Dülmer, C.; Berresheim, H.

    2008-02-01

    Detailed investigations of the chemical and microphysical properties of rural continental aerosols were performed during the HAZE2002 experiment, which was conducted in May 2002 at the Meteorological Observatory Hohenpeissenberg (DWD) in Southern Germany. Online measurements included: Size-resolved chemical composition of submicron particles; total particle number concentrations and size distributions over the diameter range of 3 nm to 9 μm; gas-phase concentration of monoterpenes, CO, O3, OH, and H2SO4. Filter sampling and offline analytical techniques were used to determine: Fine particle mass (PM2.5), organic, elemental and total carbon in PM2.5 (OC2.5, EC2.5, TC2.5), and selected organic compounds (dicarboxylic acids, polycyclic aromatic hydrocarbons, proteins). Overall, the non-refractory components of submicron particles detected by aerosol mass spectrometry (PM1, 6.6±5.4 μg m-3, arithmetic mean and standard deviation) accounted for ~62% of PM2.5 determined by filter gravimetry (10.6±4.7 μg m-3). The relative proportions of non-refractory submicron particle components were: (23±39)% ammonium nitrate, (27±23)% ammonium sulfate, and (50±40)% organics (OM1). OM1 was closely correlated with PM1 (r2=0.9) indicating a near-constant ratio of non-refractory organics and inorganics. The average ratio of OM1 to OC2.5 was 2.1±1.4, indicating a high proportion of heteroelements in the organic fraction of the sampled rural aerosol. This is consistent with the high ratio of oxygenated organic aerosol (OOA) over hydrocarbon-like organic aerosol (HOA) inferred from the AMS results (4:1), and also with the high abundance of proteins (~3%) indicating a high proportion of primary biological material (~30%) in PM2.5. This finding was confirmed by low abundance of PAHs (<1 ng m-3) and EC (<1 μg m-3) in PM2.5 and detection of several secondary organic aerosol compounds (dicarboxylic acids) and their precursors (monoterpenes). New particle formation was observed almost

  18. Source term experiments project (STEP): aerosol characterization system

    SciTech Connect

    Schlenger, B.J.; Dunn, P.F.

    1985-01-01

    A series of four experiments is being conducted at Argonne National Laboratory's TREAT Reactor. They have been designed to provide some of the necessary data regarding magnitude and release rates of fission products from degraded fuel pins, physical and chemical characteristics of released fission products, and aerosol formation and transport phenomena. These are in-pile experiments, whereby the test fuel is heated by neutron induced fission and subsequent clad oxidation in steam environments that simulate as closely as practical predicted reactor accident conditions. The test sequences cover a range of pressure and fuel heatup rate, and include the effect of Ag/In/Cd control rod material.

  19. Measurement of the ambient organic aerosol volatility distribution: application during the Finokalia Aerosol Measurement Experiment (FAME-2008)

    NASA Astrophysics Data System (ADS)

    Lee, B. H.; Kostenidou, E.; Hildebrandt, L.; Riipinen, I.; Engelhart, G. J.; Mohr, C.; Decarlo, P. F.; Mihalopoulos, N.; Prevot, A. S. H.; Baltensperger, U.; Pandis, S. N.

    2010-07-01

    A variable residence time thermodenuder (TD) was combined with an Aerodyne Aerosol Mass Spectrometer (AMS) and a Scanning Mobility Particle Sizer (SMPS) to measure the volatility distribution of aged organic aerosol in the Eastern Mediterranean during the Finokalia Aerosol Measurement Experiment in May of 2008 (FAME-2008). A new method for the quantification of the organic aerosol volatility distribution was developed combining measurements of all three instruments together with an aerosol dynamics model. Challenges in the interpretation of ambient thermodenuder-AMS measurements include the potential resistances to mass transfer during particle evaporation, the effects of particle size on the evaporated mass fraction, the changes in the AMS collection efficiency and particle density as the particles evaporate partially in the TD, and finally potential losses inside the TD. Our proposed measurement and data analysis method accounts for all of these problems combining the AMS and SMPS measurements. The AMS collection efficiency of the aerosol that passed through the TD was found to be approximately 10% lower than the collection efficiency of the aerosol that passed through the bypass. The organic aerosol measured at Finokalia is approximately 2 orders of magnitude less volatile than fresh laboratory-generated biogenic secondary organic aerosol. This low volatility is consistent with its highly oxygenated AMS mass spectrum. The results are found to be highly sensitive to the mass accommodation coefficient of the evaporating species.

  20. Aerosols containing Legionella pneumophila generated by shower heads and hot-water faucets.

    PubMed Central

    Bollin, G E; Plouffe, J F; Para, M F; Hackman, B

    1985-01-01

    Shower heads and hot-water faucets containing Legionella pneumophila were evaluated for aerosolization of the organism with a multistage cascade impaction air sampler. Air was collected above two shower doors and from the same rooms approximately 3 ft (91 cm) from the shower doors while the hot water was running. Low numbers (3 to 5 CFU/15 ft3 [0.43 m3] of air) of L. pneumophila were recovered above both shower doors, but none was recovered from the air in either room outside the shower door. Approximately 90% (7 of 8 CFU) of the L. pneumophila recovered were trapped in aerosol particles between 1 and 5 micron in diameter. Air was collected 1 to 3 ft (30 to 91 cm) from 14 sinks while the hot water was running. Low numbers (1 to 5 CFU/15 ft3 of air) were recovered from 6 of 19 air samples obtained. Approximately 50% (6 of 13 CFU) of the organisms recovered were trapped in aerosol particles between 1 and 8 microns in diameter. Shower heads and hot-water taps containing L. pneumophila can aerosolize low numbers of the organism during routine use. The aerosol particle size is small enough to penetrate to the lower human respiratory system. Thus, these sites may be implicated as a means of transmission of L. pneumophila from potable water to the patient. PMID:4091548

  1. Nitrogen Containing Organic Compounds and Oligomers in Secondary Organic Aerosol Formed by Photooxidation of Isoprene

    SciTech Connect

    Nguyen, Tran B.; Laskin, Julia; Laskin, Alexander; Nizkorodov, Serguei

    2011-07-06

    Electrospray ionization high-resolution mass spectrometry (ESI HR-MS) was used to probe molecular structures of oligomers in secondary organic aerosol (SOA) generated in laboratory experiments on isoprene photooxidation at low- and high-NOx conditions. Up to 80-90% of the observed products are oligomers and up to 33% are nitrogen-containing organic compounds (NOC). We observe oligomers with up to 8 monomer units in length. Tandem mass spectrometry (MSn) confirms NOC compounds are organic nitrates and elucidates plausible chemical building blocks contributing to oligomer formation. Most organic nitrates are comprised of methylglyceric acid units. Other important multifunctional C2-C5 monomer units are identified including methylglyoxal, hydroxyacetone, hydroxyacetic acid, glycolaldehyde, and 2-methyltetrols. The majority of the NOC oligomers contain only one nitrate moiety resulting in a low average N:C ratio of 0.019. Average O:C ratios of the detected SOA compounds are 0.54 under the low-NOx conditions and 0.83 under the high-NOx conditions. Our results underscore the importance of isoprene photooxidation as a source of NOC in organic particulate matter.

  2. AEROSOLS CONTAINING 'LEGIONELLA PNEUMOPHILA' GENERATED BY SHOWER HEADS AND HOT-WATER FAUCETS

    EPA Science Inventory

    Shower heads and hot-water faucets containing Legionella pneumophila were evaluated for aerosolization of the organism with a multistage cascade impaction air sampler. Air was collected above two shower doors and from the same rooms approximately 3 ft (91 cm) from the shower door...

  3. Seawater mesocosm experiments in the Arctic uncover differential transfer of marine bacteria to aerosols.

    PubMed

    Fahlgren, Camilla; Gómez-Consarnau, Laura; Zábori, Julia; Lindh, Markus V; Krejci, Radovan; Mårtensson, E Monica; Nilsson, Douglas; Pinhassi, Jarone

    2015-06-01

    Biogenic aerosols critically control atmospheric processes. However, although bacteria constitute major portions of living matter in seawater, bacterial aerosolization from oceanic surface layers remains poorly understood. We analysed bacterial diversity in seawater and experimentally generated aerosols from three Kongsfjorden sites, Svalbard. Construction of 16S rRNA gene clone libraries from paired seawater and aerosol samples resulted in 1294 sequences clustering into 149 bacterial and 34 phytoplankton operational taxonomic units (OTUs). Bacterial communities in aerosols differed greatly from corresponding seawater communities in three out of four experiments. Dominant populations of both seawater and aerosols were Flavobacteriia, Alphaproteobacteria and Gammaproteobacteria. Across the entire dataset, most OTUs from seawater could also be found in aerosols; in each experiment, however, several OTUs were either selectively enriched in aerosols or little aerosolized. Notably, a SAR11 clade OTU was consistently abundant in the seawater, but was recorded in significantly lower proportions in aerosols. A strikingly high proportion of colony-forming bacteria were pigmented in aerosols compared with seawater, suggesting that selection during aerosolization contributes to explaining elevated proportions of pigmented bacteria frequently observed in atmospheric samples. Our findings imply that atmospheric processes could be considerably influenced by spatiotemporal variations in the aerosolization efficiency of different marine bacteria. PMID:25682947

  4. Comparative studies of aerosol extinction measurements made by the SAM II and SAGE II satellite experiments

    NASA Technical Reports Server (NTRS)

    Yue, Glenn K.; Mccormick, M. P.; Chu, W. P.; Wang, P.; Osborn, M. T.

    1989-01-01

    Results from the Stratospheric Aerosol Measurement (SAM) II and Stratospheric Aerosol and Gas Experiment (SAGE) II are compared for measurement locations which are coincident in time and space. At 1.0 micron, the SAM II and SAGE II aerosol extinction profiles are similar within their measurement errors. In addition, sunrise and sunset aerosol extinction data at four different wavelengths are compared for occasions when the SAGE II and SAM II measurements are nearly coincident in space and about 12 hours apart.

  5. CONTAIN assessment of the NUPEC mixing experiments

    SciTech Connect

    Stamps, D.W.

    1995-08-01

    The ability of the CONTAIN code to predict the thermal hydraulics of five experiments performed in the NUPEC 1/4-scale model containment was assessed. These experiments simulated severe accident conditions in a nuclear power plant in which helium (as a nonflammable substitute for hydrogen) and steam were coinjected at different locations in the facility with and without the concurrent injection of water sprays in the dome. Helium concentrations, gas temperatures and pressures, and wall temperatures were predicted and compared with the data. The use of different flow solvers, nodalization schemes, and analysis methods for the treatment of water sprays was emphasized. As a result, a general procedure was suggested for lumped-parameter code analyses of problems in which the thermal hydraulics are dominated by water sprays.

  6. Pampre : a new laboratory experiment to better understand the physico-chemical processes of Titan aerosols formation and growth

    NASA Astrophysics Data System (ADS)

    Szopa, C.; Cernogora, G.; Boufendi, L.; Correia, J. J.; Coll, P.

    2003-04-01

    Titan s atmosphere contains aerosols issued from the organic chemistry induced by the photochemistry of N2 and CH4, the major gaseous atmospheric compounds. These organic aerosols are important as they : i) have a significant influence on the properties of the atmosphere, linked to their optical properties; ii) represent the best known example of transition from the gaseous to the solid phase by chemistry; iii) represent the most complex organics produced in Titan s atmosphere, making them particularly interesting from an exo/astrobiological point of view. However, few direct information are available about them, and their processes of formation and growth are not well understood. In order to bring answers to these questions, we developed a new type of laboratory simulation which is dedicated to better understand the physico-chemical processes involved in the formation and growth of the aerosols. The main originality of this experiment (named PAMPRE) comes from its ability to produce aerosols in volume, as they are maintained in levitation thanks to an electric force compensating gravity, whereas the other similar experiments produce tholins on the reactors walls. Thus, one should produce analogs of Titan s aerosols within representative conditions. Moreover, beyond the ex-situ analyses generally led to characterize the aerosols properties with conventional techniques (MEB, GC-MS), the experimental set-up allows to operate in situ studies of the reactive plasma by UV-vis spectroscopy, in order to deduce the electron energy distribution function which have to be compared with the sun spectrum. Beyond the characterization of the aerosols properties and formation, this experiment will also provide information and materials that will be used to operate the calibrations of the Aerosol and Collector Pyrolyser and Gas Chromatograph-Mass Spectrometer experiments of the Cassini-Huygens mission, and to develop the ICAPS-IMPF facility which should be present in the ISS within

  7. Stratospheric Aerosol and Gas Experiment (SAGE) II and III Aerosol Extinction Measurements in the Arctic Middle and Upper Troposphere

    NASA Technical Reports Server (NTRS)

    Treffeisen, R. E.; Thomason, L. W.; Strom, J.; Herber, A. B.; Burton, S. P.; Yamanouchi, T.

    2006-01-01

    In recent years, substantial effort has been expended toward understanding the impact of tropospheric aerosols on Arctic climate and chemistry. A significant part of this effort has been the collection and documentation of extensive aerosol physical and optical property data sets. However, the data sets present significant interpretive challenges because of the diverse nature of these measurements. Among the longest continuous records is that by the spaceborne Stratospheric Aerosol and Gas Experiment (SAGE) II. Although SAGE tropospheric measurements are restricted to the middle and upper troposphere, they may be able to provide significant insight into the nature and variability of tropospheric aerosol, particularly when combined with ground and airborne observations. This paper demonstrates the capacity of aerosol products from SAGE II and its follow-on experiment SAGE III to describe the temporal and vertical variations of Arctic aerosol characteristics. We find that the measurements from both instruments are consistent enough to be combined. Using this combined data set, we detect a clear annual cycle in the aerosol extinction for the middle and upper Arctic troposphere.

  8. Titan aerosol and gas experiment for the Huygens Probe

    NASA Technical Reports Server (NTRS)

    Carle, G. C.; Kojiro, D. R.; Oberbeck, V.; Ohara, B. J.; Pollack, J. B.; Valentin, J. R.; Bar-Nun, A.; Cohen, M. J.; Ferris, J. P.; Greenberg, J. M.

    1991-01-01

    The Cassini Mission is a joint undertaking of NASA and the European Space Agency (ESA) to explore the Saturnian System with a Saturn Orbiter and a Titan Probe. The launch vehicle and the Saturn Orbiter are the responsibility of NASA while the Huygens Probe (detachable Titan Probe) is the responsibility of ESA. The spacecraft will be launched in 1996 and the Huygens Probe will arrive at Titan in 2003. The Cassini Mission-Huygens Probe provides a unique opportunity to obtain detailed information about the atmosphere and, possibly, the surface of Titan. Titan possesses a substantial nitrogen atmosphere containing methane and many other organic compounds. Aerosols play an important role in the atmospheric processes on Titan. The Huygens Probe offers an opportunity to determine how organic particles are formed and grow which will clarify their role on Earth. A powerful analytical instrument, capable of addressing the above technology and other science questions, was recently proposed for the Huygens Probe. It is comprised of an aerosol and gas sampler and processor, and a gas chromatograph-ion mobility spectrometer. The instrument will be able to measure complex organics that make up the collected aerosols to the approximate 1 ppm level. Gases will be measured to approximately 10 ppb. Because the Titan atmosphere is expected to be quite complex, a gas chromatograph-ion mobility spectrometer is used to provide unequivocal identification of the components of the analytes. Further details of the science question to be investigated and the proposed instrument are described. The expected results and their implications are also addressed.

  9. MELCOR 1.8.3 assessment: CSE containment spray experiments

    SciTech Connect

    Kmetyk, L.N.

    1994-12-01

    MELCOR is a fully integrated, engineering-level computer code, being developed at Sandia National Laboratories for the USNRC, that models the entire spectrum of severe accident phenomena in a unified framework for both BWRs and PWRS. As part, of an ongoing assessment program, the MELCOR computer code has been used to analyze a series of containment spray tests performed in the Containment Systems Experiment (CSE) vessel to evaluate the performance of aqueous sprays as a means of decontaminating containment atmospheres. Basecase MELCOR results are compared with test data, and a number of sensitivity studies on input modelling parameters and options in both the spray package and the associated aerosol washout and atmosphere decontamination by sprays modelled in the radionuclide package have been done. Time-step and machine-dependency calculations were done to identify whether any numeric effects exist in these CSE assessment analyses. A significant time-step dependency due to an error in the spray package coding was identified and eliminated. A number of other code deficiencies and inconveniences also are noted.

  10. A unique approach to determine the ice nucleating potential of soot-containing aerosol from biomass combustion

    NASA Astrophysics Data System (ADS)

    Levin, E. J.; McMeeking, G. R.; McCluskey, C.; DeMott, P. J.; Kreidenweis, S. M.

    2013-12-01

    Ice nucleating particles (INP) play a crucial role in cloud and precipitation development in mixed phase clouds by catalyzing ice formation at temperatures warmer than -36 C. Despite their importance, however, there is still considerable uncertainty as to the sources and chemical nature of INP. Water insoluble particles such as mineral dust and certain biological aerosols have been shown to be efficient ice nuclei, and soot particles have also been suggested as potential INP. Biomass burning, such as wildfires and prescribed burning, is a large contributor to atmospheric soot concentrations, and could therefore be a potentially important source of INP. Both laboratory and field studies have detected enhanced INP concentrations in smoke plumes; however, the chemical composition of these INP is still uncertain as fires emit and loft a complex mixture of aerosol particles. In this work we employ a novel approach to selectively remove soot aerosol from the sample stream to determine the specific contribution of soot to INP concentrations. A number of commonly consumed biomass fuels were burned in the U.S. Forest Service combustion laboratory during the FLAME-4 (Fire Laboratory At Missoula Experiment - 4) study. Number concentrations of INP acting in the condensation and immersion freezing modes and total aerosol greater than 500 nm in diameter (N500) were measured using the Colorado State University Continuous Flow Diffusion Chamber (CFDC). To determine the contribution of soot to INP concentrations, the sample stream was passed through a Single Particle Soot Photometer (SP2; Droplet Measurement Technologies) which employs laser induced incandescence (LII) to detect soot containing particles and total soot mass. During LII, soot containing particles are vaporized and removed from the sample while non-soot containing particles pass through the instrument unaffected. By sampling the exhaust of the SP2 with the CFDC and alternately cycling laser power on and off we were

  11. Measurement of the ambient organic aerosol volatility distribution: application during the Finokalia Aerosol Measurement Experiment (FAME-2008)

    NASA Astrophysics Data System (ADS)

    Lee, B. H.; Kostenidou, E.; Hildebrandt, L.; Riipinen, I.; Engelhart, G. J.; Mohr, C.; Decarlo, P. F.; Mihalopoulos, N.; Prevot, A. S. H.; Baltensperger, U.; Pandis, S. N.

    2010-12-01

    A variable residence time thermodenuder (TD) was combined with an Aerodyne Aerosol Mass Spectrometer (AMS) and a Scanning Mobility Particle Sizer (SMPS) to measure the volatility distribution of aged organic aerosol in the Eastern Mediterranean during the Finokalia Aerosol Measurement Experiment in May of 2008 (FAME-2008). A new method for the quantification of the organic aerosol volatility distribution was developed combining measurements of all three instruments together with an aerosol dynamics model. Challenges in the interpretation of ambient thermodenuder-AMS measurements include the potential resistances to mass transfer during particle evaporation, the effects of particle size on the evaporated mass fraction, the changes in the AMS collection efficiency and particle density as the particles evaporate partially in the TD, and finally potential losses inside the TD. Our proposed measurement and data analysis method accounts for all of these problems combining the AMS and SMPS measurements. The AMS collection efficiency of the aerosol that passed through the TD was found to be approximately 10% lower than the collection efficiency of the aerosol that passed through the bypass. The organic aerosol measured at Finokalia is approximately 2 or more orders of magnitude less volatile than fresh laboratory-generated monoterpene (α-pinene, β-pinene and limonene under low NOx conditions) secondary organic aerosol. This low volatility is consistent with its highly oxygenated AMS mass spectrum. The results are found to be highly sensitive to the mass accommodation coefficient of the evaporating species. This analysis is based on the assumption that there were no significant reactions taking place inside the thermodenuder.

  12. Laboratory Experiments and Instrument Development for the Study of Atmospheric Aerosols

    SciTech Connect

    Davidovits, Paul

    2011-12-10

    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

  13. Effective Henry's Law constant measurements for glyoxal in model aerosols containing sulfate

    NASA Astrophysics Data System (ADS)

    Kampf, C.; Waxman, E.; Slowik, J.; Dommen, J.; Prevot, A.; Baltensperger, U.; Noziere, B.; Hoffmann, T.; Volkamer, R.

    2012-04-01

    Traditional models represent secondary organic aerosol (SOA) formation based on the gas-phase oxidation of a limited set of precursor molecules. However, these models tend to under-estimate the amounts and degree of oxygenation of actual SOA, indicating missing processes. One such source that has become increasingly important in recent years is glyoxal (CHOCHO, the smallest alpha-dicarbonyl). Unlike traditional SOA precursors, glyoxal forms SOA by partitioning to the aqueous phase according to Henry's Law. This work presents an analysis of Henry's Law constants for glyoxal uptake to laboratory-generated aerosols in a dynamically coupled gas-aerosol system. We combine CU LED-CE-DOAS measurements of gas-phase glyoxal with online HR-Tof-AMS and time-resolved HPLC ESI MS/MS particle-phase measurements to characterize the time resolved evolution of glyoxal partitioning, and relate molecular-specific measurements to AMS mass spectra. The experiments were performed in the simulation chamber facility at PSI, Switzerland, and investigate ammonium sulfate (AS), and mixed AS / fulvic acid seed aerosols under relative humidity conditions ranging from 50 to 85% RH. The Henry's Law and effective Henry's Law constants are compared with other values reported in the literature.

  14. Effective Henry's Law constant measurements for glyoxal in model aerosols containing sulfate

    NASA Astrophysics Data System (ADS)

    Kampf, C. J.; Waxman, E.; Slowik, J. G.; Dommen, J.; Prevot, A. S.; Noziere, B.; Hoffmann, T.; Volkamer, R.

    2011-12-01

    Traditional models represent secondary organic aerosol (SOA) formation based on the gas-phase oxidation of a limited set of precursor molecules. However, these models tend to under-estimate the amounts and degree of oxygenation of actual SOA, indicating missing processes. One such source that has become increasingly important in recent years is glyoxal (CHOCHO, the smallest alpha-dicarbonyl). Unlike traditional SOA precursors, glyoxal forms SOA by partitioning to the aqueous phase according to Henry's Law. This work presents an analysis of Henry's Law constants for glyoxal uptake to laboratory-generated aerosols in a dynamically coupled gas-aerosol system. We combine CU LED-CE-DOAS measurements of gas-phase glyoxal with online HR-Tof-AMS and time-resolved HPLC ESI MS/MS particle-phase measurements to characterize the time resolved evolution of glyoxal partitioning, and relate molecular-specific measurements to AMS mass spectra. The experiments were performed in the simulation chamber facility at PSI, Switzerland, and investigate ammonium sulfate (AS), and mixed AS / fulvic acid seed aerosols under relative humidity conditions ranging from 50 to 85% RH. The Henry's Law and effective Henry's Law constants are compared with other values reported in the literature.

  15. MELCOR 1.8.1 assessment: PNL Ice Condenser Aerosol Experiments

    SciTech Connect

    Gross, R.J.

    1993-06-01

    The MELCOR code was used to simulate PNL`s Ice Condenser Experiments 11-6 and 16-11. In these experiments, ZnS was injected into a mixing chamber, and the combined steam/air/aerosol mixture flowed into an ice condenser which was l4.7m tall. Experiment 11-6 was a low flow test; Experiment l6-1l was a high flow test. Temperatures in the ice condenser region and particle retention were measured in these tests. MELCOR predictions compared very well to the experimental data. The MELCOR calculations were also compared to CONTAIN code calculations for the same tests. A number of sensitivity studies were performed. It as found that simulation time step, aerosol parameters such as the number of MAEROS components and sections used and the particle density, and ice condenser parameters such as the energy capacity of the ice, ice heat transfer coefficient multiplier, and ice heat structure characteristic length all could affect the results. Thermal/hydraulic parameters such as control volume equilibrium assumptions, flow loss coefficients, and the bubble rise model were found to affect the results less significantly. MELCOR results were not machine dependent for this problem.

  16. An alternative treatment method for fluorosurfactant-containing wastewater by aerosol-mediated separation.

    PubMed

    Ebersbach, Ina; Ludwig, Svenja M; Constapel, Marc; Kling, Hans-Willi

    2016-09-15

    The treatment of fluorosurfactant-containing wastewater is still challenging nowadays. Here, a method is presented to remove fluorosurfactants from water, amongst others from electroplating wastewater. This elimination technique is based on the generation of gas bubbles in solution, enrichment and scavenging of fluorosurfactants by transport of the gas bubbles to the water surface. Finally the bubbles collapse and release an aerosol which is enriched with fluorosurfactants. By sampling of the released aerosols a mass balance was established for 6:2 fluorotelomer sulfonic acid (6:2 FTSA). Thereby 99.8% of the initial amount was revocered in the collected aerosols. Fluorosurfactant concentration in solution decreased exponentially with half-lives ranging from 2 to 6 min for 6:2 FTSA as well as perfluorooctane carboxylate (PFOA) and perfluorooctane sulfonate (PFOS). Elimination rate in defined matrix (0.2 M H2SO4) within 60 min was 99.6, 99.9 and 99.8% for 6:2 FTSA, PFOA and PFOS, respectively. The removal rate of 6:2 FTSA increased in solutions with higher ionic strength. Different wastewater from an electroplating industry containing 6:2 FTSA was treated with the described method without any sample pre-treatment and elimination of 6:2 FTSA took place with the same effectiveness as in synthetic matrices. PMID:27286468

  17. Effects of explosively venting aerosol-sized particles through earth-containment systems on the cloud-stabilization height

    SciTech Connect

    Dyckes, G.W.

    1980-07-01

    A method of approximating the cloud stabilization height for aerosol-sized particles vented explosively through earth containment systems is presented. The calculated values for stabilization heights are in fair agreement with those obtained experimentally.

  18. Generation and characterization of aerosols and vapors for inhalation experiments.

    PubMed Central

    Tillery, M I; Wood, G O; Ettinger, H J

    1976-01-01

    Control of aerosol and vapor characteristics that affect the toxicity of inhaled contaminants often determines the methods of generating exposure atmospheres. Generation methods for aerosols and vapors are presented. The characteristics of the resulting exposure atmosphere and the limitations of the various generation methods are discussed. Methods and instruments for measuring the airborne contaminant with respect to various charcteristics are also described. PMID:797565

  19. A comparative study of aerosol extinction measurements made by the SAM II and SAGE satellite experiments

    NASA Technical Reports Server (NTRS)

    Yue, G. K.; Mccormick, M. P.; Chu, W. P.

    1984-01-01

    SAM II and SAGE are two satellite experiments designed to measure stratospheric aerosol extinction using the technique of solar occultation or limb extinction. Although each sensor is mounted aboard a different satellite, there are occasions when their measurement locations are nearly coincident, thereby providing opportunities for a measurement comparison. In this paper, the aerosol extinction profiles and daily contour plots for some of these events in 1979 are reported. The comparisons shown in this paper demonstrate that SAM II and SAGE are producing similar aerosol extinction profiles within their measurement errors and that since SAM II has been previously validated, these results show the validity of the SAGE aerosol measurements.

  20. Effect of photochemical self-action of carbon-containing aerosol: Wildfires

    NASA Astrophysics Data System (ADS)

    Konovalov, I. B.; Berezin, E. V.; Beekmann, M.

    2016-05-01

    It has been shown by numerical simulation that the rate of formation of secondary organic aerosols (SOAs) in smoke plumes caused by vegetation and peat fires under real conditions can significantly depend on the aerosol optical thickness (AOT). The AOT determines the photodissociation rate and hydroxyl radical concentration, which in turn determines the rate of SOA generation as a result of oxidation of semivolatile organic compounds. Quantitative analysis has been carried out for the situation that took place in European Russia during the 2010 Russian wildfires. The state-of-the-art 3D chemical transport model is used in this study; the simulations are optimized and validated using the data of monitoring of the particulate matter in the Moscow region and Finland. The findings indicate that it is important to allow for this effect in studies focused on the analysis and prediction of air pollution due to wildfires, as well as climate and weather studies, whose results may depend on the assumptions about the content and properties of atmospheric carbon-containing aerosol.

  1. Organic Aerosol Formation in the Humid, Photochemically-Active Southeastern US: SOAS Experiments and Simulations

    NASA Astrophysics Data System (ADS)

    Sareen, N.; Lim, Y. B.; Carlton, A. G.; Turpin, B. J.

    2013-12-01

    Aqueous multiphase chemistry in the atmosphere can lead to rapid transformation of organic compounds, forming highly oxidized low volatility organic aerosol and, in some cases, light absorbing (brown) carbon. Because liquid water is globally abundant, this chemistry could substantially impact climate, air quality, health, and the environment. Gas-phase precursors released from biogenic and anthropogenic sources are oxidized and fragmented forming water-soluble gases that can undergo reactions in the aqueous phase (in clouds, fogs, and wet aerosols) leading to the formation of secondary organic aerosol (SOAAQ). Recent studies have highlighted the role of certain precursors like glyoxal, methylglyoxal, glycolaldehyde, acetic acid, acetone, and epoxides in the formation of SOAAQ. The goal of this work is to identify other precursors that are atmospherically important. In this study, ambient mixtures of water-soluble gases were scrubbed from the atmosphere at Brent, Alabama during the Southern Oxidant and Aerosol Study (SOAS). Four mist chambers in parallel collected ambient gases in a DI water medium at 20-25 LPM with a 4 hr collection time. Total organic carbon (TOC) values in daily composited samples were 64-180 μM. Aqueous OH radical oxidation experiments were conducted with these mixtures in a newly designed cuvette chamber to understand the formation of SOA through gas followed by aqueous chemistry. OH radicals (3.5E-2 μM [OH] s-1) were formed in-situ in the chamber, continuously by H2O2 photolysis. Precursors and products of these aqueous OH experiments were characterized using ion chromatography (IC), electrospray ionization mass spectrometry (ESI-MS), and IC-ESI-MS. ESI-MS results from a June 12th, 2013 sample showed precursors to be primarily odd, positive mode ions, indicative of the presence of non-nitrogen containing alcohols, aldehydes, organic peroxides, or epoxides. Products were seen in the negative mode and included organic acid ions like pyruvate

  2. The Stratospheric Aerosol and Gas Experiment III - International Space Station: Extending Long-Term Ozone and Aerosol Observations (Invited)

    NASA Astrophysics Data System (ADS)

    Eckman, R.; Zawodny, J. M.; Cisewski, M.; Gasbarre, J.; Flittner, D. E.; Hill, C.; Roell, M.; Moore, J. R.; Hernandez, G.; McCormick, M. P.

    2013-12-01

    The Stratospheric Aerosol and Gas Experiment III - International Space Station (SAGE III on ISS) will extend the global measurements of vertical profiles of ozone, aerosols, water vapor, nitrogen dioxide, and other trace gases begun with SAGE I in 1979, enabling the detection of long-term trends. SAGE III on ISS is the fourth in a series of instruments developed for monitoring these constituents in the stratosphere and troposphere. The SAGE III instrument is a moderate resolution spectrometer covering wavelengths from 290 nm to 1550 nm, using the heritage occultation technique, utilizing both the sun and the moon. Launch to ISS is planned for early 2015 aboard a Falcon 9 spacecraft. SAGE III will investigate the spatial and temporal variability of the measured species in order to determine their role in climatological processes, biogeochemical cycles, the hydrologic cycle, and atmospheric chemistry. It will characterize tropospheric, as well as stratospheric aerosols and upper tropospheric and stratospheric clouds, and investigate their effects on the Earth's environment including radiative, microphysical, and chemical interactions. The multi-decadal SAGE ozone and aerosol data sets have undergone intense scrutiny and are the international standard for accuracy and stability. SAGE data have been used to monitor the effectiveness of the Montreal Protocol. Amongst its key objectives will be to assess the state of the recovery in the distribution of ozone, to reestablish the aerosol measurements needed by both climate and ozone models, and to gain further insight into key processes contributing to ozone and aerosol variability. The ISS is ideal for Earth observing experiments; its mid-inclination orbit allows for a large range in latitude sampling and nearly continuous communications with payloads. In this presentation, we describe the SAGE III on ISS mission, its implementation, current status, and concentrate on its key science objectives.

  3. MAPTIP experiment, marine aerosol properties and thermal imager performance

    SciTech Connect

    Eijk, A.M.J. van; Leeuw, G. de; Jensen, D.R.

    1994-12-31

    During the fall of 1993, a field experimental study on Marine Aerosol Properties and Thermal Imager Performance (MAPTIP) was conducted in the Dutch coastal waters. The objectives of the MAPTIP trial were: (1) to improve and validate vertical marine aerosol models by providing an extensive set of aerosol and meteorological measurements, within a coastal environment, at different altitudes and for a range of meteorological conditions; (2) to make aerosol and meteorological observations in the first 10 m above the ocean surface with a view to extending existing aerosol models to incorporate near-surface effects; (3) to assess marine boundary layer effects on thermal imaging systems. Aerosol and meteorological instruments, as well as thermal imagers and calibrated targets, were used at several platforms and locations. Measurements have been made of atmospheric turbulence and refractivity effects at wavelengths in the IR and visible, to assess the marine boundary layer effects on the degradation of thermal images. Calibrated targets at different altitudes were observed to the maximum observable range under a wide variety of conditions in both the 3--5 and 8--12 gm bands, These data will be used for the development and validation of IRST models and IR ship signature models with the view of determining the effects of marine-generated aerosols, turbulence and meteorological profiles on their performance.

  4. Fire aerosol experiment and comparisons with computer code predictions

    NASA Astrophysics Data System (ADS)

    Gregory, W. S.; Nichols, B. D.; White, B. W.; Smith, P. R.; Leslie, I. H.; Corkran, J. R.

    1988-08-01

    Los Alamos National Laboratory, in cooperation with New Mexico State University, has carried on a series of tests to provide experimental data on fire-generated aerosol transport. These data will be used to verify the aerosol transport capabilities of the FIRAC computer code. FIRAC was developed by Los Alamos for the U.S. Nuclear Regulatory Commission. It is intended to be used by safety analysts to evaluate the effects of hypothetical fires on nuclear plants. One of the most significant aspects of this analysis deals with smoke and radioactive material movement throughout the plant. The tests have been carried out using an industrial furnace that can generate gas temperatures to 300 C. To date, we have used quartz aerosol with a median diameter of about 10 microns as the fire aerosol simulant. We also plan to use fire-generated aerosols of polystyrene and polymethyl methacrylate (PMMA). The test variables include two nominal gas flow rates (150 and 300 cu ft/min) and three nominal gas temperatures (ambient, 150 C, and 300 C). The test results are presented in the form of plots of aerosol deposition vs length of duct. In addition, the mass of aerosol caught in a high-efficiency particulate air (HEPA) filter during the tests is reported. The tests are simulated with the FIRAC code, and the results are compared with the experimental data.

  5. Reactive uptake of N2O5 by aerosol particles containing mixtures of humic acid and ammonium sulfate.

    PubMed

    Badger, Claire L; Griffiths, Paul T; George, Ingrid; Abbatt, Jonathan P D; Cox, R Anthony

    2006-06-01

    The kinetics of reactive uptake of N2O5 on submicron aerosol particles containing humic acid and ammonium sulfate has been investigated as a function of relative humidity (RH) and aerosol composition using a laminar flow reactor coupled with a differential mobility analyzer (DMA) to characterize the aerosol. For single-component humic acid aerosol the uptake coefficient, gamma, was found to increase from 2 to 9 x 10(-4) over the range 25-75% RH. These values are 1-2 orders of magnitude below those typically observed for single-component sulfate aerosols (Phys. Chem. Chem. Phys. 2003, 5, 3453-3463;(1) Atmos. Environ. 2000, 34, 2131-2159(2)). For the mixed aerosols, gamma was found to decrease with increasing humic acid mass fraction and increase with increasing RH. For aerosols containing only 6% humic acid by dry mass, a decrease in reactivity of more than a factor of 2 was observed compared with the case for single-component ammonium sulfate. The concentration of liquid water in the aerosol droplets was calculated using the aerosol inorganic model (for the ammonium sulfate component) and a new combined FTIR-DMA system (for the humic acid component). Analysis of the uptake coefficients using the water concentration data shows that the change in reactivity cannot be explained by the change in water content alone. We suggest that, due to its surfactant properties, the main effect of the humic acid is to reduce the mass accommodation coefficient for N2O5 at the aerosol particle surface. This has implications for the use of particle hygroscopicity data for predictions of the rate of N2O5 hydrolysis. PMID:16722713

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

    NASA Technical Reports Server (NTRS)

    Russell, Philip B.

    1994-01-01

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

  7. Remote Sensing of Spectral Aerosol Properties: A Classroom Experience

    NASA Technical Reports Server (NTRS)

    Levy, Robert C.; Pinker, Rachel T.

    2006-01-01

    Bridging the gap between current research and the classroom is a major challenge to today s instructor, especially in the sciences where progress happens quickly. NASA Goddard Space Flight Center and the University of Maryland teamed up in designing a graduate class project intended to provide a hands-on introduction to the physical basis for the retrieval of aerosol properties from state-of-the-art MODIS observations. Students learned to recognize spectral signatures of atmospheric aerosols and to perform spectral inversions. They became acquainted with the operational MODIS aerosol retrieval algorithm over oceans, and methods for its evaluation, including comparisons with groundbased AERONET sun-photometer data.

  8. Heterogeneous Ice Nucleation on Kaolinite Particles, Particle Surrogates of HUmic-Like Substances (HULIS), and Organics-Containing Urban Aerosols

    NASA Astrophysics Data System (ADS)

    Wang, B.; Knopf, D. A.

    2009-12-01

    Aerosol particles can affect the global radiation budget through aerosol-cloud interactions by acting as cloud condensation nuclei and ice nuclei (IN) thereby inducing new clouds and/or modifying the radiative properties of existing clouds. This study presents heterogeneous ice nucleation data as a function of particle temperature and relative humidity with respect to ice (RHice) for laboratory generated kaolinite particles, leonardite and fulvic acid particles serving as surrogates for aerosols composed of HULIS, and organics-containing urban aerosols collected during the MILAGRO (Mexico City) campaign. These experiments are conducted using an improved version of a previously developed ice nucleation cell coupled to an optical microscope which allows to control particle temperatures between 200-300 K and corresponding atmospherically relevant RHice. Micrometer-sized particles are deposited onto a hydrophobic substrate and are placed in the nucleation cell. To validate the experimental approach and quality of substrates, ice nucleation experiments were performed 1. on plain sample substrates and 2. using a well studied IN: kaolinite particles. The results corroborate that kaolinite particles are efficient IN inducing ice nucleation at 102-120% RHice via deposition mode at temperatures between 200 and 245 K, in agreement with previous studies. The ice nucleation efficiency of leonardite and fulvic acid particles with median diameters of 2-3 µm is determined. Leonardite particles nucleate ice via deposition mode at 120-140% RHice for temperatures between 200 and 240 K with the minimum RHice threshold observed at 220 K. Fulvic acid particles nucleate ice via deposition mode at 135-150% RHice for temperatures between 200 and 230 K with the minimum RHice threshold determined at 216 K. The fulvic acid particles take up water at RH>95% for temperatures between 235 and 250 K. The contact angle derived from experimentally determined heterogeneous ice nucleation rate

  9. Characterization of Aerosols Containing Zn, Pb, and Cl from an Industrial Region of Mexico City

    SciTech Connect

    Moffet, Ryan C; Desyaterik, Yury; Hopkins, Rebecca J; Tivanski, Alexei V; Gilles, Marry K; Wang, Yan A; Shutthanandan, V; Molina, Luisa T; Abraham, Rodrigo G; Johnson, Kirsten S; Mugica, Violeta; Molina, Mario J; Laskin, Alexander; Prather, Kimberly A

    2008-10-01

    During the March, 2006 MILAGRO campaign, measurements in the Northern Mexico City Metropolitan Area revealed the frequent appearance of particles with a characteristically high content of internally mixed Zn, Pb, Cl, and P. A comprehensive study of the chemical and physical properties of these particles was performed using a complementary combination of aerosol measurement techniques. Individual particles were analyzed using Aerosol Time-of-Flight Mass Spectrometry (ATOFMS) and Computer Controlled Scanning Electron Microscopy/Energy Dispersive X-Ray spectroscopy (CCSEM/EDX). Proton Induced X-Ray Emission (PIXE) analysis of bulk aerosol samples provided time-resolved mass concentrations of individual elements. The PIXE measurements indicated that Zn is more strongly correlated with Cl than with any other element and that Zn concentrations are higher than other non-ferrous transition metals. The Zn- and Pb - containing particles have both spherical and non-spherical morphologies. Many metal rich particles had needle-like structures and were found to be composed of ZnO and/or Zn(NO3)2∙6H2O as indicated by scanning transmission x-ray microscopy/near edge X-ray absorption spectroscopy (STXM/NEXAFS). The Zn and Pb rich particles were primarily in the submicron size range and internally mixed with elemental carbon. The unique chemical associations most closely match signatures acquired for garbage incineration. This unique combination of complementary analytical techniques has allowed for a comprehensive evaluation of Zn- and Pb- containing particles in a complex urban environment, highlighting unique characteristics that give powerful insight into their origin.

  10. Tropospheric ozone and aerosols measured by airborne lidar during the 1988 Arctic boundary layer experiment

    NASA Technical Reports Server (NTRS)

    Browell, Edward V.; Butler, Carolyn F.; Kooi, Susan A.

    1991-01-01

    Ozone (O3) and aerosol distributions were measured from an aircraft using a differential absorption lidar (DIAL) system as part of the 1988 NASA Global Tropospheric Experiment - Arctic Boundary Layer Experiment (ABLE-3A) to study the sources and sinks of gases and aerosols over the tundra regions of Alaska during the summer. The tropospheric O3 budget over the Arctic was found to be strongly influenced by stratospheric intrusions. Regions of low aerosol scattering and enhanced O3 mixing ratios were usually correlated with descending air from the upper troposphere or lower stratosphere. Several cases of continental polar air masses were examined during the experiment. The aerosol scattering associated with these air masses was very low, and the atmospheric distribution of aerosols was quite homogeneous for those air masses that had been transported over the ice for greater than or = 3 days. The transition in O3 and aerosol distributions from tundra to marine conditions was examined several times. The aerosol data clearly show an abrupt change in aerosol scattering properties within the mixed layer from lower values over the tundra to generally higher values over the water. The distinct differences in the heights of the mixed layers in the two regions was also readily apparent. Several cases of enhanced O3 were observed during ABLE-3 in conjunction with enhanced aerosol scattering in layers in the free atmosphere. Examples are presented of the large scale variations of O3 and aerosols observed with the airborne lidar system from near the surface to above the tropopause over the Arctic during ABLE-3.

  11. Note: A portable laser induced breakdown spectroscopy instrument for rapid sampling and analysis of silicon-containing aerosols

    NASA Astrophysics Data System (ADS)

    McLaughlin, R. P.; Mason, G. S.; Miller, A. L.; Stipe, C. B.; Kearns, J. D.; Prier, M. W.; Rarick, J. D.

    2016-05-01

    A portable instrument has been developed for measuring silicon-containing aerosols in near real-time using laser-induced breakdown spectroscopy (LIBS). The instrument uses a vacuum system to collect and deposit airborne particulate matter onto a translatable reel of filter tape. LIBS is used to analyze the deposited material, determining the amount of silicon-containing compounds present. In laboratory testing with pure silica (SiO2), the correlation between LIBS intensity for a characteristic silicon emission and the concentration of silica in a model aerosol was determined for a range of concentrations, demonstrating the instrument's plausibility for identifying hazardous levels of silicon-containing compounds.

  12. Note: A portable laser induced breakdown spectroscopy instrument for rapid sampling and analysis of silicon-containing aerosols.

    PubMed

    McLaughlin, R P; Mason, G S; Miller, A L; Stipe, C B; Kearns, J D; Prier, M W; Rarick, J D

    2016-05-01

    A portable instrument has been developed for measuring silicon-containing aerosols in near real-time using laser-induced breakdown spectroscopy (LIBS). The instrument uses a vacuum system to collect and deposit airborne particulate matter onto a translatable reel of filter tape. LIBS is used to analyze the deposited material, determining the amount of silicon-containing compounds present. In laboratory testing with pure silica (SiO2), the correlation between LIBS intensity for a characteristic silicon emission and the concentration of silica in a model aerosol was determined for a range of concentrations, demonstrating the instrument's plausibility for identifying hazardous levels of silicon-containing compounds. PMID:27250478

  13. EFFECT OF AN ACTIVATED SLUDGE WASTEWATER TREATMENT PLANT ON AMBIENT AIR DENSITIES OF AEROSOLS CONTAINING BACTERIA AND VIRUSES

    EPA Science Inventory

    Bacteria and virus-containing aerosols were studied during late summer and fall in a U.S. midwestern suburb before and during the start up and operation of an unenclosed activated sludge wastewater treatment plant. The air in this suburban area contained low-level densities of in...

  14. Laboratory experiments on the formation and recoil jet transport of aerosol by laser ablation

    NASA Astrophysics Data System (ADS)

    Hirooka, Yoshi; Tanaka, Kazuo A.; Imamura, Keisuke; Okazaki, Katsuya

    2016-05-01

    In a high-repetition rate inertial fusion reactor, the first wall will be subjected to repeated ablation along with pellet implosions, which then leads to the formation of aerosol to scatter and/or deflect laser beams for the subsequent implosion, affecting the overall reactor performance. Proposed in the present work is a method of in-situ directed transport of aerosol particles by the use of laser ablation-induced jet recoil momenta. Lithium and carbon are used as the primary ablation targets, the former of which is known to form aerosol in the form of droplet, and the latter of which tends to form carbon nanotubes. Laboratory-scale experiments have been conducted to irradiate airborne aerosol particles with high-intensity laser to produce ablation-induced jet. Data have indicated a change in aerosol flow direction, but only in the case of lithium.

  15. A Global Aerosol Model Forecast for the ACE-Asia Field Experiment

    NASA Technical Reports Server (NTRS)

    Chin, Mian; Ginoux, Paul; Lucchesi, Robert; Huebert, Barry; Weber, Rodney; Anderson, Tad; Masonis, Sarah; Blomquist, Byron; Bandy, Alan; Thornton, Donald

    2003-01-01

    We present the results of aerosol forecast during the Aerosol Characterization Experiment (ACE-Asia) field experiment in spring 2001, using the Georgia Tech/Goddard Global Ozone Chemistry Aerosol Radiation and Transport (GOCART) model and the meteorological forecast fields from the Goddard Earth Observing System Data Assimilation System (GEOS DAS). The aerosol model forecast provides direct information on aerosol optical thickness and concentrations, enabling effective flight planning, while feedbacks from measurements constantly evaluate the model, making successful model improvements. We verify the model forecast skill by comparing model predicted total aerosol extinction, dust, sulfate, and SO2 concentrations with those quantities measured by the C-130 aircraft during the ACE-Asia intensive operation period. The GEOS DAS meteorological forecast system shows excellent skills in predicting winds, relative humidity, and temperature for the ACE-Asia experiment area as well as for each individual flight, with skill scores usually above 0.7. The model is also skillful in forecast of pollution aerosols, with most scores above 0.5. The model correctly predicted the dust outbreak events and their trans-Pacific transport, but it constantly missed the high dust concentrations observed in the boundary layer. We attribute this missing dust source to the desertification regions in the Inner Mongolia Province in China, which have developed in recent years but were not included in the model during forecasting. After incorporating the desertification sources, the model is able to reproduce the observed high dust concentrations at low altitudes over the Yellow Sea. Two key elements for a successful aerosol model forecast are correct source locations that determine where the emissions take place, and realistic forecast winds and convection that determine where the aerosols are transported. We demonstrate that our global model can not only account for the large

  16. Comparison of Aerosol Single Scattering Albedos Derived by Diverse Techniques In Two North Atlantic Experiments

    NASA Technical Reports Server (NTRS)

    Russell, P. B.; Redemann, J.; Schmid, B.; Bergstrom, R. W.; Livingston, J. M.; McIntosh, D. M.; Ramirez, S. A.; Hartley, S.; Hobbs, P. V.; Quinn, P. K.

    2002-01-01

    Aerosol single scattering albedo omega (the ratio of scattering to extinction) is important in determining aerosol climatic effects, in explaining relationships between calculated and measured radiative fluxes, and in retrieving aerosol optical depths from satellite radiances. Recently, two experiments in the North Atlantic region, the Tropospheric Aerosol Radiative Forcing Observational Experiment (TARFOX) and the Second Aerosol Characterization Experiment (ACE-2), determined aerosol omega by a variety of techniques. The techniques included fitting of calculated to measured radiative fluxes; retrievals of omega from skylight radiances; best fits of complex refractive index to profiles of backscatter extinction, and size distribution; and in situ measurements of scattering and absorption at the surface and aloft. Both TARFOX and ACE-2 found a fairly wide range of values for omega at midvisable wavelengths approx. 550 nm, with omega(sub midvis) greater than or equal to 0.85 and less than or equal to 0.99 for the marine aerosol impacted by continental pollution. Frequency distributions of omega could usually be approximated by lognormals in omega(sub max) - omega, with some occurrence of bimodality, suggesting the influence of different aerosol sources or processing. In both TARFOX and ACE-2, closure tests between measured and calculated radiative fluxes yielded best-fit values of omega(sub midvis) 0.90 +/- 0.04 for the polluted boundary layer. Although these results have the virtue of describing the column aerosol unperturbed by sampling, they are subject to questions about representativeness and other uncertainties (e.g., thermal offsets, unknown gas absorption) The other techniques gave larger values for omega(sub midvis) for the polluted boundary layer, with a typical result of omega(sub midvis) = 0.95 +/- 0.04. Current uncertainties in omega are large in terms of climate effects More tests are needed of the consistency among different methods and of

  17. Visible and near infrared observation on the Global Aerosol Backscatter Experiment (GLOBE)

    NASA Technical Reports Server (NTRS)

    Spinhirne, James D.; Cavanaugh, John F.; Chudamani, S.; Bufton, Jack L.; Sullivan, Robert J.

    1991-01-01

    The Global Aerosol Backscatter Experiment (GLOBE) was intended to provide data on prevailing values of atmospheric backscatter cross-section. The primary intent was predicting the performance of spaceborne lidar systems, most notably the Laser Atmospheric Wind Sounder (LAWS) for the Earth Observing System (EOS). The second and related goal was to understand the source and characteristics of atmospheric aerosol particles. From the GLOBE flights, extensive data was obtained on the structure of clouds and the marine planetary boundary layer. A notable result for all observations is the consistency of the large increases in the aerosol scattering ratio for the marine boundary layer. Other results are noted.

  18. Effect of an activated sludge wastewater treatment plant on ambient air densities of aerosols containing bacteria and viruses.

    PubMed

    Fannin, K F; Vana, S C; Jakubowski, W

    1985-05-01

    Bacteria- and virus-containing aerosols were studied during the late summer and fall seasons in a midwestern suburb of the United States before and during the start-up and operation of an unenclosed activated sludge wastewater treatment plant. The study showed that the air in this suburban area contained low-level densities of indicator microorganisms. After the plant began operating, the densities of total aerobic bacteria-containing particles, standard plate count bacteria, total coliforms, fecal coliforms, fecal streptococci, and coliphages increased significantly in the air within the perimeter of the plant. Before plant operations, bacteria were detected from five genera, Klebsiella, Enterobacter, Serratia, Salmonella, and Aeromonas. During plant operations, the number of genera identified increased to 11. In addition to those genera found before plant operations, Escherichia, Providencia, Citrobacter, Acinetobacter, Pasteurella, and Proteus, were also identified. Enteric viruses were detected in low densities from the air emissions of this plant. Only standard plate count bacteria remained at significantly higher than base-line densities beyond 250 m downwind from the center of the aeration tanks. Fecal streptococci and coliphages appeared to be more stable in aerosols than the other indicator microorganisms studied. In general, the densities of microorganism-containing aerosols were higher at night than during the day. The techniques used in this study may be employed to establish microorganism-containing aerosol exposure during epidemiological investigations. PMID:2988442

  19. Stratospheric Aerosol and Gas Experiment III on the International Space Station (SAGE III/ISS)

    NASA Technical Reports Server (NTRS)

    Gasbarre, Joseph; Walker, Richard; Cisewski, Michael; Zawodny, Joseph; Cheek, Dianne; Thornton, Brooke

    2015-01-01

    The Stratospheric Aerosol and Gas Experiment III on the International Space Station (SAGE III/ISS) mission will extend the SAGE data record from the ideal vantage point of the International Space Station (ISS). The ISS orbital inclination is ideal for SAGE measurements providing coverage between 70 deg north and 70 deg south latitude. The SAGE data record includes an extensively validated data set including aerosol optical depth data dating to the Stratospheric Aerosol Measurement (SAM) experiments in 1975 and 1978 and stratospheric ozone profile data dating to the Stratospheric Aerosol and Gas Experiment (SAGE) in 1979. These and subsequent data records, notably from the SAGE II experiment launched on the Earth Radiation Budget Satellite in 1984 and the SAGE III experiment launched on the Russian Meteor-3M satellite in 2001, have supported a robust, long-term assessment of key atmospheric constituents. These scientific measurements provide the basis for the analysis of five of the nine critical constituents (aerosols, ozone (O3), nitrogen dioxide (NO2), water vapor (H2O), and air density using O2) identified in the U.S. National Plan for Stratospheric Monitoring. SAGE III on ISS was originally scheduled to fly on the ISS in the same timeframe as the Meteor-3M mission, but was postponed due to delays in ISS construction. The project was re-established in 2009.

  20. Aerosol lofting from sea breeze during the Indian Ocean Experiment

    NASA Astrophysics Data System (ADS)

    Verma, S.; Boucher, O.; Venkataraman, C.; Reddy, M. S.; Müller, D.; Chazette, P.; Crouzille, B.

    2006-04-01

    This work was carried out to understand the mechanisms leading to lofting and large-scale advection of aerosols over the Indian Ocean region due to interaction of the sea breeze with the northeast monsoon winds along the west coast of India. European Centre for Medium-Range Weather Forecasts (ECMWF) wind fields for the months of February and March 1999 were analyzed at various times of day. Intense sea breeze activity was observed at 1200 UT (1730 local time) along the west coast of India with average intensity larger in March than in February. The sea breeze was seen to extend inland deeper in March than in February. Lofting of air observed as high as 800 hPa (approximately 2 km above sea level) could lead to entrainment of aerosols into the free troposphere and long-range transport. Upward motion of air was observed everywhere along the west coast of India (from 8° to 20°N), on average higher in March than in February, because of convergence between the sea breeze and the synoptic-scale flow. A region of intense lofting of air and well-defined convergence was observed along the coast of the Karnataka region (12°-16°N). A simulation with a general circulation model nudged with ECMWF data indicated that the intrusion of marine air masses with low concentrations of organic matter is seen as deep as 64 km inland in the evening (1500 UT). Intrusion of the sea-salt plume is seen to a maximum distance of around 200 km from 1500 until 2300 UT. A well-developed lofted layer of aerosols as high as 3 km was also simulated during sea breeze activity along the west coast of India. The general circulation model simulation shows a clear diurnal evolution of the vertical profile of the aerosol extinction coefficient at Goa but fails to reproduce several features of the lidar observations, for example, the marked diurnal variability of the upper layers between 1 and 3 km. However, the model simulates a diurnal cycle at the surface (0-0.7 km) that is not apparent in lidar

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

    NASA Technical Reports Server (NTRS)

    Lau, William K. M.

    2008-01-01

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

  2. Diffusion battery sampling of sulfuric acid aerosols formed in oleum spill experiments

    SciTech Connect

    Tang, I N; Wong, W T; Munkelwitz, H R

    1980-01-01

    Fuming sulfuric acid (oleum) is one of several hazardous chemicals routinely transported in bulk quantities on US waterways. In the event of a marine accident, a large amount of the cargo acid could suddenly be released into water, resulting in the formation of a dense sulfuric acid cloud. Experiments were carried out in the laboratory to study the factors controlling the extent of acid aerosol formation under conditions likely to occur in maritime spill accidents. A Sinclair-type diffusion battery was used for aerosol sizing. In this presentation, a brief discussion of an improved nonlinear iterative inversion method for the analysis of diffusion battery data is given. Experimental results obtained with monodisperse test aerosols and sulfuric acid aerosols formed during oleum spills are presented. It is shown that the diffusion battery, coupled with the inversion technique, is capable of sizing particles up to 0.8 ..mu..m in diameter.

  3. Experiments with the assimilation of fine aerosols using an ensemble Kalman filter

    NASA Astrophysics Data System (ADS)

    Pagowski, Mariusz; Grell, Georg A.

    2012-11-01

    In a series of experiments we issue forecasts of fine aerosol concentration over the coterminous USA and southern Canada using the Weather Research and Forecasting - Chemistry model initialized with 3D-VAR or ensemble Kalman filter (EnKF) assimilation methods. Assimilated observations include surface measurements of fine aerosols from the United States Environmental Protection Agency AIRNow Data Exchange program. Evaluation statistics calculated over a month-and-half-long summer period demonstrate the advantage of EnKF over 3D-VAR and point to the limitations of applying a simple aerosol parameterization for predicting air quality over the forecast area. Strategies for further improvement of forecasting aerosol concentrations are discussed.

  4. Experience and Challenges in Implementing Stratospheric Aerosol Gas Experiment on Meteor-3M Platform

    NASA Technical Reports Server (NTRS)

    Habib, Shahid; Newsom, Jerry; Rawls, Richard

    2001-01-01

    Implementation of Stratospheric Aerosol Gas Experiment (SAGE) is a joint science mission between the Rosavioskosmos, also called Russian Aviation and Space Agency (RASA) and the National Aeronautics and Space Administration (NASA). Under the global collaboration agreement established by President Clinton and Yeltsin in 1995 between the United States and Russia, space was one of the major areas identified for joint scientific collaboration. There were several collaborative projects identified under space, earth, human exploration of space and aeronautics. SAGE was one of the key Earth Science instruments selected common to both countries' interests in ozone research. SAGE has a long space heritage, and four earlier versions of this instrument have flown in space for the last 15-year period. It has provided a vital ozone and aerosol data in the mid latitudes and has contributed in the overall ozone depletion research. SAGE II, the fourth instrument has been flying in space on NASA's Earth Radiation Budget Satellite (ERBS) for the last 14 years. Ball Aerospace built the instrument under Langley Research Center's (LaRC) management. SAGE III for Russian Meteor-3M mission is a third generation design with more spectral bands, elaborate data gathering and storage and intelligent terrestrial software. The Russian collaboration required a complete integration of SAGE III on the Russian Meteor-3M satellite and a launch on a Zenit-2 launch vehicle manufactured in Ukraine. The whole complex is scheduled to be launched from Baikonur cosmodrome in early 2001. This cooperative mission has presented a number of management, technical and logistical challenges on both sides. This paper makes an attempt to review and document such experiences.

  5. Chemical Composition and Cloud Condensation Nuclei Properties of Marine Aerosols during the 2005 Marine Stratus Experiment

    NASA Astrophysics Data System (ADS)

    Lee, Y.; Hudson, J.; Daum, P.; Springston, S.; Wang, J.; Senum, G.; Alexander, L.; Jayne, J.; Hubbe, J.

    2006-12-01

    Marine aerosol chemical composition and cloud condensation nuclei (CCN) spectrum were determined on board the DOE G1 aircraft during the Marine Stratus Experiment conducted over the coastal waters between Point Reyes National Seashore and Monterey Bay, California, in July 2005. Aerosol components, including sea-salt- (sodium, chloride, magnesium, methansulfonate) and terrestrial/pollution-derived (ammonium, sulfate, nitrate, organics, potassium, and calcium) were measured using the particle-into-liquid sampler-ion chromatography technique and an Aerodyne AMS at a time resolution of 4 min and 30 s, respectively, both covering the size range of ~0.08 to 1.5 micrometers. The CCN spectrum was determined at a 1-s time resolution covering a supersaturation range between 0.02% and 1%. The accumulation mode particle size- number distribution was measured using a passive cavity aerosol spectrometer probe; the cloud droplet size- number distribution was determined using a Cloud Aerosol Probe. During the campaign sulfate/organic aerosols were always present, sea-salt aerosols were observed on half of the flights, and no dust or biomass burning contribution was noted as calcium and potassium were always below their limits-of-detection. Based on CCN spectra and cloud droplet number concentrations, the typical supersaturation of the marine stratus clouds was ~0.06%, corresponding to a CCN critical diameter between 0.1 and 0.2 micrometer. This large critical diameter makes the aerosol chemical composition measured appropriate for investigating the CCN properties and marine stratus clouds. We note that while sea-salt aerosols and sulfate aerosols were most likely externally mixed, the ensemble exhibits similar CCN properties irrespective of the relative mass concentrations of these two types of aerosols, owing partly to the similar activation properties of NaCl and (NH4)2SO4 aerosols, and that sea-salt particles were larger but fewer, accounting for a small fraction of cloud

  6. Characterizing the impact of urban emissions on regional aerosol particles: airborne measurements during the MEGAPOLI experiment

    NASA Astrophysics Data System (ADS)

    Freney, E. J.; Sellegri, K.; Canonaco, F.; Colomb, A.; Borbon, A.; Michoud, V.; Doussin, J.-F.; Crumeyrolle, S.; Amarouche, N.; Pichon, J.-M.; Bourianne, T.; Gomes, L.; Prevot, A. S. H.; Beekmann, M.; Schwarzenböeck, A.

    2014-02-01

    The MEGAPOLI (Megacities: Emissions, urban, regional and Global Atmospheric POLlution and climate effects, and Integrated tools for assessment and mitigation) experiment took place in July 2009. The aim of this campaign was to study the aging and reactions of aerosol and gas-phase emissions in the city of Paris. Three ground-based measurement sites and several mobile platforms including instrument equipped vehicles and the ATR-42 aircraft were involved. We present here the variations in particle- and gas-phase species over the city of Paris, using a combination of high-time resolution measurements aboard the ATR-42 aircraft. Particle chemical composition was measured using a compact time-of-flight aerosol mass spectrometer (C-ToF-AMS), giving detailed information on the non-refractory submicron aerosol species. The mass concentration of black carbon (BC), measured by a particle absorption soot photometer (PSAP), was used as a marker to identify the urban pollution plume boundaries. Aerosol mass concentrations and composition were affected by air-mass history, with air masses that spent longest time over land having highest fractions of organic aerosol and higher total mass concentrations. The Paris plume is mainly composed of organic aerosol (OA), BC, and nitrate aerosol, as well as high concentrations of anthropogenic gas-phase species such as toluene, benzene, and NOx. Using BC and CO as tracers for air-mass dilution, we observe the ratio of ΔOA / ΔBC and ΔOA / ΔCO increase with increasing photochemical age (-log(NOx / NOy)). Plotting the equivalent ratios of different organic aerosol species (LV-OOA, SV-OOA, and HOA) illustrate that the increase in OA is a result of secondary organic aerosol (SOA) formation. Within Paris the changes in the ΔOA / ΔCO are similar to those observed during other studies in London, Mexico City, and in New England, USA. Using the measured SOA volatile organic compounds (VOCs) species together with organic aerosol formation

  7. Characterizing the impact of urban emissions on regional aerosol particles; airborne measurements during the MEGAPOLI experiment

    NASA Astrophysics Data System (ADS)

    Freney, E. J.; Sellegri, K.; Canonaco, F.; Colomb, A.; Borbon, A.; Michoud, V.; Doussin, J.-F.; Crumeyrolle, S.; Amarouch, N.; Pichon, J.-M.; Prévôt, A. S. H.; Beekmann, M.; Schwarzenböeck, A.

    2013-09-01

    The MEGAPOLI experiment took place in July 2009. The aim of this campaign was to study the aging and reactions of aerosol and gas-phase emissions in the city of Paris. Three ground-based measurement sites and several mobile platforms including instrument equipped vehicles and the ATR-42 aircraft were involved. We present here the variations in particle- and gas-phase species over the city of Paris using a combination of high-time resolution measurements aboard the ATR-42 aircraft. Particle chemical composition was measured using a compact time-of-flight aerosol mass spectrometer (C-ToF-AMS) giving detailed information of the non-refractory submicron aerosol species. The mass concentration of BC, measured by a particle absorption soot photometer (PSAP), was used as a marker to identify the urban pollution plume boundaries. Aerosol mass concentrations and composition were affected by air-mass history, with air masses that spent longest time over land having highest fractions of organic aerosol and higher total mass concentrations. The Paris plume is mainly composed of organic aerosol (OA), black carbon and nitrate aerosol, as well as high concentrations of anthropogenic gas-phase species such as toluene, benzene, and NOx. Using BC and CO as tracers for air-mass dilution, we observe the ratio of ΔOA / ΔBC and ΔOA / ΔCO increase with increasing photochemical age (-log(NOx / NOy). Plotting the equivalent ratios for the Positive Matrix Factorization (PMF) resolved species (LV-OOA, SV-OOA, and HOA) illustrate that the increase in OA is a result of secondary organic aerosol (SOA). Within Paris the changes in the ΔOA / ΔCO are similar to those observed during other studies in Mexico city, Mexico and in New England, USA. Using the measured VOCs species together with recent organic aerosol formation yields we predicted ~ 50% of the measured organics. These airborne measurements during the MEGAPOLI experiment show that urban emissions contribute to the formation of OA

  8. ARM Cloud Aerosol Precipitation Experiment (ACAPEX) Science Plan

    SciTech Connect

    Leung, L. R.; Prather, K.; Ralph, R.; Rosenfeld, D.; Spackman, R.; DeMott, P.; Fairall, C.; Fan, J.; Hagos, S.; Hughes, M.; Long, C.; Rutledge, S.; Waliser, D.; Wang, H.

    2014-09-01

    The western U.S. receives precipitation predominantly during the cold season when storms approach from the Pacific Ocean. The snowpack that accumulates during winter storms provides about 70-90% of water supply for the region. Understanding and modeling the fundamental processes that govern the large precipitation variability and extremes in the western U.S. is a critical test for the ability of climate models to predict the regional water cycle, including floods and droughts. Two elements of significant importance in predicting precipitation variability in the western U.S. are atmospheric rivers and aerosols. Atmospheric rivers (ARs) are narrow bands of enhanced water vapor associated with the warm sector of extratropical cyclones over the Pacific and Atlantic oceans. Because of the large lower-tropospheric water vapor content, strong atmospheric winds and neutral moist static stability, some ARs can produce heavy precipitation by orographic enhancement during landfall on the U.S. West Coast. While ARs are responsible for a large fraction of heavy precipitation in that region during winter, much of the rest of the orographic precipitation occurs in post-frontal clouds, which are typically quite shallow, with tops just high enough to pass the mountain barrier. Such clouds are inherently quite susceptible to aerosol effects on both warm rain and ice precipitation-forming processes.

  9. Exploring Atmospheric Aqueous Chemistry (and Secondary Organic Aerosol Formation) through OH Radical Oxidation Experiments, Droplet Evaporation and Chemical Modeling

    NASA Astrophysics Data System (ADS)

    Turpin, B. J.; Kirkland, J. R.; Lim, Y. B.; Ortiz-Montalvo, D. L.; Sullivan, A.; Häkkinen, S.; Schwier, A. N.; Tan, Y.; McNeill, V. F.; Collett, J. L.; Skog, K.; Keutsch, F. N.; Sareen, N.; Carlton, A. G.; Decesari, S.; Facchini, C.

    2013-12-01

    effective vapor pressures that are orders of magnitude lower when ammonium hydroxide is present (pH 7) than without (at lower pH). In Po Valley experiments, nitrogen-containing organics were prominent precursors and intermediates. Pyruvate and oxalate were among the products. Importantly, formation of aqSOA helps to explain the high O/C ratios found in atmospheric aerosols. While uncertainties remain large, global modeling suggests that aqSOA is comparable in magnitude to SOA formed through gas phase chemistry and vapor pressure driven partitioning (gasSOA).

  10. Aerosol Properties over the Indo-Gangetic Plain: A Mesoscale Perspective from the TIGERZ Experiment

    NASA Technical Reports Server (NTRS)

    Giles, David M.; Holben, Brent N.; Tripathi, Sachchida; Eck, Thomas F.; Newcomb, W. Wayne; Slutsker, Ilya; Dickerson, Russell R.; Thompson, Anne M.; Mattoo, Shana; Wang, Sheng-Hsiang; Singh, Remesh P.; Sinyuk, Aliaksandr; Schafer, Joel S.

    2011-01-01

    High aerosol loading over the northern Indian subcontinent can result in poor air quality leading to human health consequences and climate perturbations. The international 2008 TIGERZ experiment intensive operational period (IOP) was conducted in the Indo \\Gangetic Plain (IGP) around the industrial city of Kanpur (26.51degN, 80.23deg E), India, during the premonsoon (April-June). Aerosol Robotic Network (AERONET) Sun photometers performed frequent measurements of aerosol properties at temporary sites distributed within an area covering 50 sq km around Kanpur to characterize pollution and dust in a region where complex aerosol mixtures and semi \\bright surface effects complicate satellite retrieval algorithms. TIGERZ IOP Sun photometers quantified aerosol optical depth (AOD) increases up to 0.10 within and downwind of the city, with urban emissions accounting for 10 C20% of the IGP aerosol loading on deployment days. TIGERZ IOP area \\averaged volume size distribution and single scattering albedo retrievals indicated spatially homogeneous, uniformly sized, spectrally absorbing pollution and dust particles. Aerosol absorption and size relationships were used to categorize black carbon and dust as dominant absorbers and to identify a third category in which both black carbon and dust dominate absorption.Moderate Resolution Imaging Spectroradiometer (MODIS) AOD retrievals with the lowest quality assurance (QA > or = 0) flags were biased high with respect to TIGERZ IOP area \\averaged measurements. MODIS AOD retrievals with QA 0 had moderate correlation (R(sup 2) = 0.52-69) with the Kanpur AERONET site, whereas retrievals with QA > 0 were limited in number. Mesoscale \\distributed Sun photometers quantified temporal and spatial variability of aerosol properties, and these results were used to validate satellite retrievals.

  11. Formation of nitrogen- and sulfur-containing light-absorbing compounds accelerated by evaporation of water from secondary organic aerosols

    NASA Astrophysics Data System (ADS)

    Nguyen, Tran B.; Lee, Paula B.; Updyke, Katelyn M.; Bones, David L.; Laskin, Julia; Laskin, Alexander; Nizkorodov, Sergey A.

    2012-01-01

    Aqueous extracts of secondary organic aerosols (SOA) generated from the ozonolysis of d-limonene were subjected to dissolution, evaporation, and re-dissolution in the presence and absence of ammonium sulfate (AS). Evaporation with AS at pH 4-9 produced chromophores that were stable with respect to hydrolysis and had a distinctive absorption band at 500 nm. Evaporation accelerated the rate of chromophore formation by at least three orders of magnitude compared to the reaction in aqueous solution, which produced similar compounds. Absorption spectroscopy and high-resolution nanospray desorption electrospray ionization (nano-DESI) mass spectrometry experiments suggested that the molar fraction of the chromophores was small (<2%), and that they contained nitrogen atoms. Although the colored products represented only a small fraction of SOA, their large extinction coefficients (>105 L mol-1 cm-1 at 500 nm) increased the effective mass absorption coefficient of the residual organics in excess of 103 cm2 g-1 - a dramatic effect on the optical properties from minor constituents. Evaporation of SOA extracts in the absence of AS resulted in the production of colored compounds only when the SOA extract was acidified to pH ˜ 2 with sulfuric acid. These chromophores were produced by acid-catalyzed aldol condensation, followed by a conversion into organosulfates. The presence of organosulfates was confirmed by high resolution mass spectrometry experiments. Results of this study suggest that evaporation of cloud or fog droplets containing dissolved organics leads to significant modification of the molecular composition and serves as a potentially important source of light-absorbing compounds.

  12. Formation of Nitrogen- and Sulfur-Containing Light-Absorbing Compounds Accelerated by Evaporation of Water from Secondary Organic Aerosols

    SciTech Connect

    Nguyen, Tran B.; Lee, Paula B.; Updyke, Katelyn M.; Bones, David L.; Laskin, Julia; Laskin, Alexander; Nizkorodov, Sergey

    2012-01-14

    Aqueous extracts of secondary organic aerosols (SOA) generated from the ozonolysis of dlimonene were subjected to dissolution, evaporation, and re-dissolution in the presence and absence of ammonium sulfate (AS). Evaporation with AS at pH 4-9 produced chromophores that were stable with respect to hydrolysis and had a distinctive absorption band at 500 nm. Evaporation accelerated the rate of chromophore formation by at least three orders of magnitude compared to the reaction in aqueous solution, which produced similar compounds. Absorption spectroscopy and high-resolution nanospray desorption electrospray ionization (nano-DESI) mass spectrometry experiments suggested that the molar fraction of the chromophores was small (< 2%), and that they contained nitrogen atoms. Although the colored products represented only a small fraction of SOA, their large extinction coefficients (>10{sup 5} L mol{sup -1} cm{sup -1} at 500 nm) increased the effective mass absorption coefficient of the residual organics in excess of 10{sup 3} cm{sup 2} g{sup -1} - a dramatic effect on the optical properties from minor constituents. Evaporation of SOA extracts in the absence of AS resulted in the production of colored compounds only when the SOA extract was acidified to pH {approx} 2 with sulfuric acid. These chromophores were produced by acid-catalyzed aldol condensation, followed by a conversion into organosulfates. The presence of organosulfates was confirmed by high resolution mass spectrometry experiments. Results of this study suggest that evaporation of cloud or fog droplets containing dissolved organics leads to significant modification of the molecular composition and serves as a potentially important source of light-absorbing compounds.

  13. T-matrix modeling of linear depolarization by morphologically complex soot and soot-containing aerosols

    NASA Astrophysics Data System (ADS)

    Mishchenko, Michael I.; Liu, Li; Mackowski, Daniel W.

    2013-07-01

    We use state-of-the-art public-domain Fortran codes based on the T-matrix method to calculate orientation and ensemble averaged scattering matrix elements for a variety of morphologically complex black carbon (BC) and BC-containing aerosol particles, with a special emphasis on the linear depolarization ratio (LDR). We explain theoretically the quasi-Rayleigh LDR peak at side-scattering angles typical of low-density soot fractals and conclude that the measurement of this feature enables one to evaluate the compactness state of BC clusters and trace the evolution of low-density fluffy fractals into densely packed aggregates. We show that small backscattering LDRs measured with ground-based, airborne, and spaceborne lidars for fresh smoke generally agree with the values predicted theoretically for fluffy BC fractals and densely packed near-spheroidal BC aggregates. To reproduce higher lidar LDRs observed for aged smoke, one needs alternative particle models such as shape mixtures of BC spheroids or cylinders.

  14. T-Matrix Modeling of Linear Depolarization by Morphologically Complex Soot and Soot-Containing Aerosols

    NASA Technical Reports Server (NTRS)

    Mishchenko, Michael I.; Liu, Li; Mackowski, Daniel W.

    2013-01-01

    We use state-of-the-art public-domain Fortran codes based on the T-matrix method to calculate orientation and ensemble averaged scattering matrix elements for a variety of morphologically complex black carbon (BC) and BC-containing aerosol particles, with a special emphasis on the linear depolarization ratio (LDR). We explain theoretically the quasi-Rayleigh LDR peak at side-scattering angles typical of low-density soot fractals and conclude that the measurement of this feature enables one to evaluate the compactness state of BC clusters and trace the evolution of low-density fluffy fractals into densely packed aggregates. We show that small backscattering LDRs measured with groundbased, airborne, and spaceborne lidars for fresh smoke generally agree with the values predicted theoretically for fluffy BC fractals and densely packed near-spheroidal BC aggregates. To reproduce higher lidar LDRs observed for aged smoke, one needs alternative particle models such as shape mixtures of BC spheroids or cylinders.

  15. Comparison of stratospheric aerosol and gas experiment I (SAGE I) and Umkehr ozone profiles including a search for Umkehr aerosol effects

    SciTech Connect

    Newchurch, M.J.

    1986-01-01

    After briefly reviewing ozone depletion predictions from atmospheric models and results from trend analysis of Umkehr data, this paper outlines the Umkehr method for deducing the vertical profile of ozone and reviews the theoretical and empirical studies of the aerosol effect on Umkehr measurements. A brief description of the Stratospheric Aerosol and Gas Experiment I (SAGE I) is followed by a method for approximating the best representation of the conditions over the Umkehr ground site as seen by the SAGE I satellite. Using a spatially weighted average of SAGE I events derived from an autocorrelation analysis, the authors find 337 co-located SAGE I and Umkehr events. The approximate total column ozone measured by SAGE I is 5% higher than that measured by Umkehr on average. Most of this difference resides in Umkehr layer two, three, and four, while layers seven, eight, and nine contain small differences in average ozone content. Intercomparison with four other ozone studies indicates agreement between SAGE I and SBUV in most layers and at most Umkehr stations north of 30/sup 0/. However, significant differences in Umkehr layer eight between SAGE I and SBUV remain. Ozone differences between SAGE I and Umkehr are strong functions of both total column ozone and season in the lower layers but not in the upper layers.

  16. Comparison of Coincident Multiangle Imaging Spectroradiometer and Moderate Resolution Imaging Spectroradiometer Aerosol Optical Depths over Land and Ocean Scenes Containing Aerosol Robotic Network Sites

    NASA Technical Reports Server (NTRS)

    Abdou, Wedad A.; Diner, David J.; Martonchik, John V.; Bruegge, Carol J.; Kahn, Ralph A.; Gaitley, Barbara J.; Crean, Kathleen A.; Remer, Lorraine A.; Holben, Brent

    2005-01-01

    The Multiangle Imaging Spectroradiometer (MISR) and the Moderate Resolution Imaging Spectroradiometer (MODIS), launched on 18 December 1999 aboard the Terra spacecraft, are making global observations of top-of-atmosphere (TOA) radiances. Aerosol optical depths and particle properties are independently retrieved from these radiances using methodologies and algorithms that make use of the instruments corresponding designs. This paper compares instantaneous optical depths retrieved from simultaneous and collocated radiances measured by the two instruments at locations containing sites within the Aerosol Robotic Network (AERONET). A set of 318 MISR and MODIS images, obtained during the months of March, June, and September 2002 at 62 AERONET sites, were used in this study. The results show that over land, MODIS aerosol optical depths at 470 and 660 nm are larger than those retrieved from MISR by about 35% and 10% on average, respectively, when all land surface types are included in the regression. The differences decrease when coastal and desert areas are excluded. For optical depths retrieved over ocean, MISR is on average about 0.1 and 0.05 higher than MODIS in the 470 and 660 nm bands, respectively. Part of this difference is due to radiometric calibration and is reduced to about 0.01 and 0.03 when recently derived band-to-band adjustments in the MISR radiometry are incorporated. Comparisons with AERONET data show similar patterns.

  17. Aerosol-Cloud Interactions Evaluated with Aircraft Measurements during the Marine Stratus Experiment (MASE)"

    NASA Astrophysics Data System (ADS)

    Conant, W. C.; Arnott, P.; Bucholtz, A.; Buzorius, G.; Chuang, P. Y.; Jonsson, H. H.; Murphy, S. M.; Rissman, T. A.; Small, J. D.; Sorooshian, A.; Varutbangkul, V.; Flagan, R. C.; Seinfeld, J. H.

    2005-12-01

    In this presentation we explore how aerosols influence the microphysical, dynamical, and radiative properties of marine stratocumulus clouds. We address these aerosol-cloud interactions using data collected by the CIRPAS Twin Otter aircraft during the MASE (Marine Stratus Experiment) campaign, which was conducted off the coast of northern California in July of this year. The otter was instrumented to measure aerosol number concentration, size distribution from 15 nm - 2500 nm, composition (TOF-AMS; PILS), and light absorption. Furthermore, an array of optical probes on the aircraft provided detailed information on the cloud microphysics, including droplet concentration, size distribution, liquid water content and precipitation size distribution. Pyranometers measuring upwelling and downwelling solar irradiance (0.3 μm - 3.5 μm) mounted on a stabilized radiometer platform were used to obtain cloud albedo immediately above the region that was being profiled. Localized (2-20 km wide) regions of high aerosol concentration in the marine boundary layer (MBL) were found and identified as "ship tracks", although no coincident features were immediately apparent in the visible satellite images. Vertical profiles were conducted by the Twin Otter within and on both sides of each ship track to obtain the contrast in aerosol and cloud properties. The ship emissions enhanced aerosol number concentration by factors ranging from 2 to more than 10. They contribute almost entirely to sulfate aerosol -- there was virtually no change in organic aerosol concentration measured by the Aerodyne TOF-AMS or light absorption measured by a photoacoustic instrument within the tracks. The ship emissions are found to have a significant impact on the cloud microphysics, including nearly a doubling of droplet concentration and a reduction in effective radius. The change in droplet dispersion is found to be important in understanding the indirect effect. Cloud albedo tended to be slightly enhanced

  18. Bedding disposal cabinet for containment of aerosols generated by animal cage cleaning procedures.

    PubMed Central

    Baldwin, C L; Sabel, F L; Henke, C B

    1976-01-01

    Laboratory tests with aerosolized spores and animal room tests with uranine dye indicate the effectiveness of a prototype bedding disposal cabinet in reducing airborne contamination generated by cage cleaning procedures. Images PMID:826219

  19. Bedding disposal cabinet for containment of aerosols generated by animal cage cleaning procedures.

    PubMed

    Baldwin, C L; Sabel, F L; Henke, C B

    1976-02-01

    Laboratory tests with aerosolized spores and animal room tests with uranine dye indicate the effectiveness of a prototype bedding disposal cabinet in reducing airborne contamination generated by cage cleaning procedures. PMID:826219

  20. The Stratospheric Aerosol and Gas Experiment III instrument proposed for EOS - A conceptual design

    NASA Technical Reports Server (NTRS)

    Mauldin, L. E.; Mccormick, M. P.; Zawodny, J. M.; Mcmaster, L. R.; Chu, W. P.; Gustafson, J. C.; Maddrea, G. L.

    1989-01-01

    This paper describes the Stratospheric Aerosol and Gas Experiment III (SAGE III) instrument proposed for the Earth Observing System (EOS), which is designed to monitor the vertical distribution of stratospheric aerosols, ozone, water vapor, nitrogen dioxide, and temperature by measuring the extinction and scattering of solar radiation in the 03 to 1.6 micron range through the atmosphere. The SAGE III employs proven concepts which have evolved from the SAM II, SAGE, and SAGE II programs. The launch is scheduled for the summer of 1996. The SAGE II block diagram is included.

  1. Comparison of Aerosol Single Scattering Albedos Derived By Diverse Techniques in Two North Atlantic Experiments

    NASA Technical Reports Server (NTRS)

    Russell, P. B.; Redemann, J.; Schmid, B.; Bergstrom, R. W.; Livingston, J. M.; McIntosh, D. M.; Hartley, S.; Hobbs, P. V.; Quinn, P. K.; Carrico, C. M.; Hipskind, R. Stephen (Technical Monitor)

    2000-01-01

    Aerosol single scattering albedo w (the ratio of scattering to extinction) is important in determining aerosol climatic effects, in explaining relationships between calculated and measured radiative fluxes, and in retrieving aerosol optical depths from satellite radiances. Recently, two experiments in the North Atlantic region, TARFOX and ACE-2, determined aerosol w by a variety of techniques. The techniques included fitting of calculated to measured fluxes; retrievals of w from skylight radiances; best fits of complex refractive index to profiles of backscatter, extinction, and size distribution; and in situ measurements of scattering and absorption at the surface and aloft. Both TARFOX and ACE-2 found a fairly wide range of values for w at midvisible wavelengths, with 0.85 less than wmidvis less than 0.99 for the marine aerosol impacted by continental pollution. Frequency distributions of w could usually be approximated by lognormals in wmax-w, with some occurrence of bimodality, suggesting the influence of different aerosol sources or processing. In both TARFOX and ACE-2, closure tests between measured and calculated radiative fluxes yielded best-fit values of wmidvis of 0.90+/-0.04 for the polluted boundary layer. Although these results have the virtue of describing the column aerosol unperturbed by sampling, they are subject to questions about representativeness and possible artifacts (e.g., unknown gas absorption). The other techniques gave larger values for wmidvis for the polluted boundary layer, with a typical result of wmidvis = 0.95+/-0.04, Current uncertainties in vv are large in terms of climate effects. More tests are needed of the consistency among different methods and of humidification effects on w.

  2. Analytical pyrolysis experiments of Titan aerosol analogues in preparation for the Cassini Huygens mission

    NASA Technical Reports Server (NTRS)

    Ehrenfreund, P.; Boon, J. J.; Commandeur, J.; Sagan, C.; Thompson, W. R.; Khare, B.

    1995-01-01

    Comparative pyrolysis mass spectrometric data of Titan aerosol analogs, called 'tholins', are presented. The Titan tholins were produced in the laboratory at Cornell by irradiation of simulated Titan atmospheres with high energy electrons in plasma discharge. Mass-spectrometry measurements were performed at FOM of the solid phase of various tholins by Curie-point pyrolysis Gas-Chromatography/Mass-Spectrometry (GCMS) and by temperature resolved in-source Pyrolysis Mass-Spectrometry to reveal the composition and evolution temperature of the dissociation products. The results presented here are used to further define the ACP (Aerosol Collector Pyrolyser)-GCMS experiment and provide a basis for modelling of aerosol composition on Titan and for the iterpretation of Titan atmosphere data from the Huygens probe in the future.

  3. Particle size distribution of aerosols sprayed from household hand-pump sprays containing fluorine-based and silicone-based compounds.

    PubMed

    Kawakami, Tsuyoshi; Isama, Kazuo; Ikarashi, Yoshiaki

    2015-01-01

    Japan has published safety guideline on waterproof aerosol sprays. Furthermore, the Aerosol Industry Association of Japan has adopted voluntary regulations on waterproof aerosol sprays. Aerosol particles of diameter less than 10 µm are considered as "fine particles". In order to avoid acute lung injury, this size fraction should account for less than 0.6% of the sprayed aerosol particles. In contrast, the particle size distribution of aerosols released by hand-pump sprays containing fluorine-based or silicone-based compounds have not been investigated in Japan. Thus, the present study investigated the aerosol particle size distribution of 16 household hand-pump sprays. In 4 samples, the ratio of fine particles in aerosols exceeded 0.6%. This study confirmed that several hand-pump sprays available in the Japanese market can spray fine particles. Since the hand-pump sprays use water as a solvent and their ingredients may be more hydrophilic than those of aerosol sprays, the concepts related to the safety of aerosol-sprays do not apply to the hand pump sprays. Therefore, it may be required for the hand-pump spray to develop a suitable method for evaluating the toxicity and to establish the safety guideline. PMID:26821469

  4. Organics Substantially Reduce HO2 Uptake onto Aerosols Containing Transition Metal ions.

    PubMed

    Lakey, Pascale S J; George, Ingrid J; Baeza-Romero, Maria T; Whalley, Lisa K; Heard, Dwayne E

    2016-03-10

    A HO2 mass accommodation coefficient of α = 0.23 ± 0.07 was measured onto submicron copper(II)-doped ammonium sulfate aerosols at a relative humidity of 60 ± 3%, at 293 ± 2 K and at an initial HO2 concentration of ∼ 1 × 10(9) molecules cm(-3) by using an aerosol flow tube coupled to a sensitive fluorescence assay by gas expansion (FAGE) HO2 detection system. The effect upon the HO2 uptake coefficient γ of adding different organic species (malonic acid, citric acid, 1,2-diaminoethane, tartronic acid, ethylenediaminetetraacetic acid (EDTA), and oxalic acid) into the copper(II)-doped aerosols was investigated. The HO2 uptake coefficient decreased steadily from the mass accommodation value to γ = 0.008 ± 0.009 when EDTA was added in a one-to-one molar ratio with the copper(II) ions, and to γ = 0.003 ± 0.004 when oxalic acid was added into the aerosol in a ten-to-one molar ratio with the copper(II). EDTA binds strongly to copper(II) ions, potentially making them unavailable for catalytic destruction of HO2, and could also be acting as a surfactant or changing the viscosity of the aerosol. The addition of oxalic acid to the aerosol potentially forms low-volatility copper-oxalate complexes that reduce the uptake of HO2 either by changing the viscosity of the aerosol or by causing precipitation out of the aerosol forming a coating. It is likely that there is a high enough oxalate to copper(II) ion ratio in many types of atmospheric aerosols to decrease the HO2 uptake coefficient. No observable change in the HO2 uptake coefficient was measured when the other organic species (malonic acid, citric acid, 1,2-diaminoethane, and tartronic acid) were added in a ten-to-one molar ratio with the copper(II) ions. PMID:26484935

  5. Ground-based aerosol characterization during the South American Biomass Burning Analysis (SAMBBA) field experiment

    NASA Astrophysics Data System (ADS)

    Brito, J.; Rizzo, L. V.; Morgan, W. T.; Coe, H.; Johnson, B.; Haywood, J.; Longo, K.; Freitas, S.; Andreae, M. O.; Artaxo, P.

    2014-11-01

    This paper investigates the physical and chemical characteristics of aerosols at ground level at a site heavily impacted by biomass burning. The site is located near Porto Velho, Rondônia, in the southwestern part of the Brazilian Amazon rainforest, and was selected for the deployment of a large suite of instruments, among them an Aerosol Chemical Speciation Monitor. Our measurements were made during the South American Biomass Burning Analysis (SAMBBA) field experiment, which consisted of a combination of aircraft and ground-based measurements over Brazil, aimed to investigate the impacts of biomass burning emissions on climate, air quality, and numerical weather prediction over South America. The campaign took place during the dry season and the transition to the wet season in September/October 2012. During most of the campaign, the site was impacted by regional biomass burning pollution (average CO mixing ratio of 0.6 ppm), occasionally superimposed by intense (up to 2 ppm of CO), freshly emitted biomass burning plumes. Aerosol number concentrations ranged from ~1000 cm-3 to peaks of up to 35 000 cm-3 (during biomass burning (BB) events, corresponding to an average submicron mass mean concentrations of 13.7 μg m-3 and peak concentrations close to 100 μg m-3. Organic aerosol strongly dominated the submicron non-refractory composition, with an average concentration of 11.4 μg m-3. The inorganic species, NH4, SO4, NO3, and Cl, were observed, on average, at concentrations of 0.44, 0.34, 0.19, and 0.01 μg m-3, respectively. Equivalent black carbon (BCe) ranged from 0.2 to 5.5 μg m-3, with an average concentration of 1.3 μg m-3. During BB peaks, organics accounted for over 90% of total mass (submicron non-refractory plus BCe), among the highest values described in the literature. We examined the ageing of biomass burning organic aerosol (BBOA) using the changes in the H : C and O : C ratios, and found that throughout most of the aerosol processing (O : C &cong

  6. The Stratospheric Aerosol and Gas Experiment (SAGE III) on the International Space Station (ISS) Mission

    NASA Technical Reports Server (NTRS)

    Cisewski, Michael; Zawodny, Joseph; Gasbarre, Joseph; Eckman, Richard; Topiwala, Nandkishore; Rodriquez-Alvarez, Otilia; Cheek, Dianne; Hall, Steve

    2014-01-01

    The Stratospheric Aerosol and Gas Experiment III on the International Space Station (SAGE III/ISS) mission will provide the science community with high-vertical resolution and nearly global observations of ozone, aerosols, water vapor, nitrogen dioxide, and other trace gas species in the stratosphere and upper-troposphere. SAGE III/ISS measurements will extend the long-term Stratospheric Aerosol Measurement (SAM) and SAGE data record begun in the 1970s. The multi-decadal SAGE ozone and aerosol data sets have undergone intense scrutiny and are considered the international standard for accuracy and stability. SAGE data have been used to monitor the effectiveness of the Montreal Protocol. Key objectives of the mission are to assess the state of the recovery in the distribution of ozone, to re-establish the aerosol measurements needed by both climate and ozone models, and to gain further insight into key processes contributing to ozone and aerosol variability. The space station mid-inclination orbit allows for a large range in latitude sampling and nearly continuous communications with payloads. The SAGE III instrument is the fifth in a series of instruments developed for monitoring atmospheric constituents with high vertical resolution. The SAGE III instrument is a moderate resolution spectrometer covering wavelengths from 290 nm to 1550 nm. Science data is collected in solar occultation mode, lunar occultation mode, and limb scatter measurement mode. A SpaceX Falcon 9 launch vehicle will provide access to space. Mounted in the unpressurized section of the Dragon trunk, SAGE III will be robotically removed from the Dragon and installed on the space station. SAGE III/ISS will be mounted to the ExPRESS Logistics Carrier-4 (ELC-4) location on the starboard side of the station. To facilitate a nadir view from this location, a Nadir Viewing Platform (NVP) payload was developed which mounts between the carrier and the SAGE III Instrument Payload (IP).

  7. Ground based aerosol characterization during the South American Biomass Burning Analysis (SAMBBA) field experiment

    NASA Astrophysics Data System (ADS)

    Brito, J.; Rizzo, L. V.; Morgan, W. T.; Coe, H.; Johnson, B.; Haywood, J.; Longo, K.; Freitas, S.; Andreae, M. O.; Artaxo, P.

    2014-05-01

    This paper investigates the physical and chemical characteristics of aerosols at ground level at a site heavily impacted by biomass burning. The site is located near Porto Velho, Rondônia, in the Southwestern part of the Brazilian Amazon forest, and was selected for the deployment of a large suite of instruments, among them an Aerosol Chemical Speciation Monitor. Our measurements were made during the South American Biomass Burning Analysis (SAMBBA) field experiment, which consisted of a combination of aircraft and ground based measurements over Brazil, aiming to investigate the impacts of biomass burning emissions on climate, air quality, and numerical weather prediction over South America. The campaign took place during the dry season and the transition to the wet season in September/October 2012. During most of the campaign, the site was impacted by regional biomass burning pollution (average CO mixing ratio of 0.6 ppm), occasionally superimposed by intense (up to 2 ppm of CO), freshly emitted biomass burning plumes. Aerosol number concentrations ranged from ∼1000 cm-3 to peaks of up to 35 000 cm-3 during biomass burning (BB) events, corresponding to an average submicron mass mean concentrations of 13.7 μg m-3 and peak concentrations close to 100 μg m-3. Organic aerosol strongly dominated the submicron non-refractory composition, with an average concentration of 11.4 μg m-3. The inorganic species, NH4, SO4, NO3, and Cl, were observed on average at concentrations of 0.44, 0.34, 0.19, and 0.01 μg m-3, respectively. Equivalent Black Carbon (BCe) ranged from 0.2 to 5.5 μg m-3, with an average concentration of 1.3 μg m-3. During BB peaks, organics accounted for over 90% of total mass (submicron non-refractory plus BCe), among the highest values described in the literature. We examined the ageing of Biomass Burning Organic Aerosol (BBOA) using the changes in the H : C and O : C ratios, and found that throughout most of the aerosol processing (O : C ≅ 0

  8. Aerosol Composition, Chemistry, and Source Characterization during the 2008 VOCALS Experiment

    NASA Astrophysics Data System (ADS)

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

    2009-12-01

    Chemical composition of fine aerosol particles over the northern Chilean coastal waters was determined on board the US DOE G-1 aircraft during the VOCALS (VAMOS Ocean-Cloud-Atmosphere-Land Study) field experiment between October 16 and November 15, 2008. Chemical species determined included SO42-, NO3-, NH4+, and total organics (Org) using an Aerodyne Aerosol Mass Spectrometer, and SO42-, NO3-, NH4+, Na+, Cl-, CH3SO3-, Mg2+, Ca2+, and K+ 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 ~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 believed to be externally mixed with the acidic sulfate aerosols. Nitrate was observed only on sea-salt particles, consistent with adsorption of HNO3 on non-acidic sea-salt aerosols, responsible partly 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 in the study domain were substantial (~0.5 - ~3 μg/m3) with a strong gradient (highest near the shore decreasing with distance from land), and the ocean-emitted dimethylsulfide and its unique oxidation product, CH3SO3-, were very low (i.e., ≤ 40 parts per trillion and <0.05 μg/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

  9. Dust and polluted aerosol impacts on diazotrophy during a mesocosm experiment in the Eastern Mediterranean Sea

    NASA Astrophysics Data System (ADS)

    Rahav, Eyal; Herut, Barak; Liu, Hongbin; Guo, Cui; Cheung, Isaac; Psarra, Stella; Lagaria, Anna; Tsiola, Anastasia; Tsagaraki, Tanya; Pitta, Paraskevi; Mulholland, Margaret; Berman-Frank, Ilana

    2014-05-01

    Atmospheric inputs of nutrients via dust and aerosols to the surface ocean layer are considered to contribute greatly to dinitrogen (N2) fixation and to primary productivity. N2 fixation rates in the Mediterranean Sea are typically low and the parameters limiting this process are still unclear. Addition of dust analogs to a mesocosm experiment in the Western Mediterranean Sea (DUNE) enhanced N2 fixation by 3 to 5 fold. However, in the Eastern Mediterranean Sea, an area highly exposed to Saharan dust and aerosol, the impact of these inputs on N2 fixation from onboard microcosm experiment are unclear and inconclusive. We examined the influence of Saharan dust (1.6 mg L-1) and polluted aerosol (1 mg L-1) additions on diazotroph populations and N2 fixation rates in nine 3 m3 mesocosms (MESOAQUA project) using the enriched seawater method of 15N uptake. The enrichments induced an immediate 2-4 fold increase in N2 fixation (measured from 6 to 48 h after enrichments). After 4 days, N2 fixation rates returned to their background level and no significant change was observed relative to the control mesocosms. The increase in N2 fixation rates were reflected in the differential composition of diazotrophs. Dust enrichment enhanced the abundance of the filamentous cyanobacterium Trichodesmium spp., while aerosol addition predominantly enhanced the presence of heterotrophic diazotrophs including Pseudomonas and Desulfovibrio. Our results indicate that sources of nutrients supplied via Saharan dust and polluted aerosol pulses to the stratified surface Eastern Mediterranean waters could increase the contribution of diazotrophs and N2 fixation in these ultraoligotrophic waters and impact productivity and biogeochemical cycling.

  10. CARBON CONTAINING COMPONENT OF THE LOS ANGELES AEROSOL: SOURCE APPORTIONMENT AND CONTRIBUTIONS TO THE VISIBILITY BUDGET

    EPA Science Inventory

    Source resolution of the organic component of the fine fraction of the ambient aerosol (d(sub p) < 3.5 micrometers) has been carried out by combining source information from the organic component with thermal analysis and local emission inventories. The primary and secondary carb...

  11. The CalWater 2 - ARM Cloud Aerosol Precipitation Experiment (ACAPEX)

    NASA Astrophysics Data System (ADS)

    Leung, L. Y.; Prather, K. A.; Ralph, F. M.; Rosenfeld, D.; Spackman, J. R.; Fairall, C. W.; DeMott, P. J.; Fan, J.; Zhao, C.

    2014-12-01

    The western U.S. receives precipitation predominantly during the cold season when storms approach from the Pacific Ocean. The snowpack that accumulates during winter storms provides about 70-90% of water supply for the region. Two elements of significant importance in predicting precipitation variability in the western U.S. are atmospheric rivers and aerosols. Atmospheric rivers (ARs) are narrow bands of enhanced water vapor associated with the warm sector of extratropical cyclones over the Pacific and Atlantic oceans. While ARs are responsible for a large fraction of heavy precipitation in the western U.S. during winter, much of the rest of the orographic precipitation occurs in post-frontal clouds, which are typically quite shallow, with tops just high enough to pass the mountain barrier. Such clouds are inherently quite susceptible to aerosol effects on both warm rain and ice precipitation-forming processes. In January - March 2015, the ARM Cloud Aerosol Precipitation Experiment (ACAPEX) field campaign will take place in northern California. Joined with CalWater 2, the field campaign aims to improve understanding and modeling of large-scale dynamics and cloud and precipitation processes associated with ARs and aerosol-cloud interactions that influence precipitation variability and extremes in the western U.S. We will implement an observational strategy consisting of the use of land and offshore assets to monitor (1) the evolution and structure of ARs from near their regions of development, (2) long range transport of aerosols in eastern North Pacific and potential interactions with ARs, and (3) how aerosols from long-range transport and local sources influence cloud and precipitation in the U.S. West Coast where ARs make landfall and post-frontal clouds are frequent. This presentation will provide an overview of the science questions and hypotheses to be addressed by CalWater 2/ACAPEX, review key results from prior studies, and discuss recent findings from

  12. AATSR Single View Satellite Aerosol Retrievals Over the Persian Gulf During the 2004 United Arabic Emirates Unified Aerosol Experiment (UAE2)

    NASA Astrophysics Data System (ADS)

    Schoemaker, R. M.

    2006-12-01

    During the months of August and September 2004 the United Arabic Emirates Unified Aerosol Experiment (UAE2) mission took place in the marine and desert region of the United Arabic Emirates. One of the primary goals of the mission was to evaluate and improve scientific based satellite aerosol and ocean retrieval products. Important aspect was the calibration and validation of remote sensing systems in order to gain more insight in space-based retrievals over this part of the region. This paper contributes to part of the space-based mission objectives and governs the retrieval of atmospheric aerosol properties over water through data from the AATSR instrument on board the European ENVISAT satellite. At TNO Defence, Security and Safety the retrieval of aerosol properties from AATSR is performed by means of the dual view algorithm for application over land and the single view algorithm for application over ocean. Both algorithms have been merged into a fast and efficient algorithm that allows for near real-time processing and which is suitable for semi-operational use. Data from retrievals over water have been compared with ground-truth measurements from the AERONET sun photometers present for the three water sites in the Persian Gulf during the campaign. The properties retrieved are a) aerosol optical depth for the visible wavelengths of AATSR and b) the Ångström wavelength coefficient α as an indicator for the size distribution. Different aerosol types have been pre-modeled by means of AERONET phase function information, and saved as look-up tables for the retrieval procedure. By comparing the satellite retrieved information with the ground-truth data for each of the modeled aerosol type more insight in the retrieval procedure and in the aerosol make-up in this region is obtained.

  13. Raman lidar and sun photometer measurements of aerosols and water vapor during the ARM RCS experiment

    NASA Technical Reports Server (NTRS)

    Ferrare, R. A.; Whiteman, D. N.; Melfi, S. H.; Evans, K. D.; Holben, B. N.

    1995-01-01

    The first Atmospheric Radiation Measurement (ARM) Remote Cloud Study (RCS) Intensive Operations Period (IOP) was held during April 1994 at the Southern Great Plains (SGP) Cloud and Radiation Testbed (CART) site near Lamont, Oklahoma. This experiment was conducted to evaluate and calibrate state-of-the-art, ground based remote sensing instruments and to use the data acquired by these instruments to validate retrieval algorithms developed under the ARM program. These activities are part of an overall plan to assess general circulation model (GCM) parameterization research. Since radiation processes are one of the key areas included in this parameterization research, measurements of water vapor and aerosols are required because of the important roles these atmospheric constituents play in radiative transfer. Two instruments were deployed during this IOP to measure water vapor and aerosols and study their relationship. The NASA/Goddard Space Flight Center (GSFC) Scanning Raman Lidar (SRL) acquired water vapor and aerosol profile data during 15 nights of operations. The lidar acquired vertical profiles as well as nearly horizontal profiles directed near an instrumented 60 meter tower. Aerosol optical thickness, phase function, size distribution, and integrated water vapor were derived from measurements with a multiband automatic sun and sky scanning radiometer deployed at this site.

  14. A new inversion for Stratospheric Aerosol and Gas Experiment II data

    NASA Astrophysics Data System (ADS)

    Rusch, D. W.; Randall, C. E.; Callan, M. T.; Horanyi, M.; Clancy, R. T.; Solomon, S. C.; Oltmans, S. J.; Johnson, B. J.; Koehler, U.; Claude, H.; de Muer, D.

    1998-04-01

    We describe a new inversion algorithm for retrieving ozone densities and aerosol extinctions from Stratospheric Aerosol and Gas Experiment (SAGE) II measurements. The primary differences between the new algorithm and the current operational SAGE II inversion are the order of the species and altitude inversions, and the methods used to calculate aerosol extinction and remove saturated signals. Ozone densities retrieved at altitudes from 15 to 30 km using the new algorithm are compared to those from the operational SAGE II inversion, as well as to ozone densities from coincident balloon ozonesonde measurements at four different locations in the northern hemisphere between 1984 and 1991 for low to medium stratospheric aerosol loading conditions. The results of the comparison show that the ozone densities resulting from the operational and new algorithms agree to within 1% above 22 km. Below 22 km, the new results are lower than the operational results by up to 30%, depending on altitude and location. At all four stations the new results agree better with the sondes, decreasing the SAGE II/sonde differences by a factor of 2 or more.

  15. Experiment to Characterize Aircraft Volatile Aerosol and Trace-Species Emissions (EXCAVATE)

    NASA Technical Reports Server (NTRS)

    Anderson, B. E.; Branham, H.-S.; Hudgins, C. H.; Plant, J. V.; Ballenthin, J. O.; Miller, T. M.; Viggiano, A. A.; Blake, D. R.; Boudries, H.; Canagaratna, M.

    2005-01-01

    The Experiment to Characterize Aircraft Volatile and Trace Species Emissions (EXCAVATE) was conducted at Langley Research Center (LaRC) in January 2002 and focused upon assaying the production of aerosols and aerosol precursors by a modern commercial aircraft, the Langley B757, during ground-based operation. Remaining uncertainty in the postcombustion fate of jet fuel sulfur contaminants, the need for data to test new theories of particle formation and growth within engine exhaust plumes, and the need for observations to develop air quality models for predicting pollution levels in airport terminal areas were the primary factors motivating the experiment. NASA's Atmospheric Effects of Aviation Project (AEAP) and the Ultra Effect Engine Technology (UEET) Program sponsored the experiment which had the specific objectives of determining ion densities; the fraction of fuel S converted from S(IV) to S(VI); the concentration and speciation of volatile aerosols and black carbon; and gas-phase concentrations of long-chain hydrocarbon and PAH species, all as functions of engine power, fuel composition, and plume age.

  16. Moisture dynamics in the cloudy and polluted tropical atmosphere: The Cloud Aerosol Radiative Forcing Dynamics Experiment (CARDEX)

    NASA Astrophysics Data System (ADS)

    Wilcox, E. M.; Thomas, R. M.; Praveen, P. S.; Pistone, K.; Bender, F.; Feng, Y.; Ramanathan, V.

    2012-12-01

    Aerosols are well known to modify the microphysical properties of clouds. This modification is expected to yield brighter clouds that cover a greater area. However, observations from satellites show little inter-hemispheric difference in cloud optical thickness and liquid water path in spite of the clear inter-hemispheric difference in aerosol optical thickness. Furthermore, comparisons of observations with global atmospheric models suggest that models that parameterize the mechanisms of aerosol nucleation of cloud drops but do not resolve cloud-scale dynamics may be overestimating the magnitude of aerosol effects on cloud radiative forcing. Resolving these discrepancies requires a deeper understanding of the factors determining the transport of moisture to the cloud layer and the effects of aerosols on that transport. Towards this goal, we have conducted a new field experiment to study the moisture dynamics in the boundary layer and lower troposphere of the polluted and cloudy tropical atmosphere. The Cloud Aerosol Radiative Forcing Dynamics Experiment (CARDEX) was conducted during the winter of 2012 at the Maldives Climate Observatory - Hanimaadhoo in the tropical northern Indian Ocean during the period of extensive outflow of the South Asian pollution. Pollution in the CARDEX region has been well documented to both modify the microphysical properties of low clouds and strongly absorb solar radiation with significant consequences for the lower atmosphere and surface radiative energy budgets. Three unmanned aerial vehicles (UAVs) flew nearly 60 research flights instrumented to measure turbulent latent and sensible heat fluxes, aerosol concentrations, and cloud microphysical properties. Airborne measurements were enhanced with continuous surface monitoring of surface turbulent heat fluxes, aerosol concentrations and physical properties, surface remote sensing of cloud water amount and aerosol profiles, and model analyses of aerosols and dynamics with WRFchem. This

  17. Characterization of mineral dust aerosols during the Saharan Dust Experiment (SHADE)

    NASA Astrophysics Data System (ADS)

    Léon, J.-F.; Tanré, D.; Haywood, J.; Pelon, J.; Kaufman, Y. J.

    2003-04-01

    Aerosols are known to be important in determining the Earth’s radiative balance. Dust aerosols are particularly interesting since, in addition to their scattering and absorbing properties that affect the solar radiation, they also perturb the terrestrial radiation. In addition, recent studies have shown that a significant proportion of mineral dust in the atmosphere may be of anthropogenic origin and therefore they may have an important role in climate change by exerting a significant radiative forcing. The Saharan Dust Experiment was designed to better determine the parameters that are relevant for computing the direct radiative effect of mineral dust. Two aircraft combining in situ measurements and remote sensing instruments were coordinated with satellite overpasses during the experiment which was based in Cape Verde during the period September 20-28, 2000. These in-situ and remotely sensed data provide valuable information on the microphysical, optical properties and radiative effects of a very large mineral dust outbreak with aerosol optical thickness up to 1.5. A new approach based on a synergy between active (lidar) and passive (spaceborne radiometer) remote sensing has been used to investigate the vertical structure of the dust plume. The retrieved profiles of extinction compare well with in situ aircraft measurements. Profiles derived from lidar measurements on September 25 highlight the presence of the so-called Saharan Air Layer, located between 2.2 and 4.5 km. Another dust layer within the sub-Saharan transition layer over the marine boundary layer is also observed. In this second layer, the effective radius of particles is significantly smaller than in the aloft layer. The trajectory analyses and the Total Mapping Ozone Spectrometer Aerosol Index suggest that the aerosols present at 1500m originates from West Mauritania. The higher aerosol layer originates from southern Algeria which confirms the difference of altitude of the dust transport

  18. A comparison of the Stratospheric Aerosol and Gas Experiment II tropospheric water vapor to radiosonde measurements

    NASA Astrophysics Data System (ADS)

    Larsen, J. C.; Chiou, E. W.; Chu, W. P.; McCormick, M. P.; McMaster, L. R.; Oltmans, S.; Rind, D.

    1993-03-01

    Upper tropospheric Stratospheric Aerosol and Gas Experiment II (SAGE II) water vapor observations are compared to correlative radiosonde observations and radiosonde based climatologies. The SAGE II 1987 monthly zonal mean water vapor climatology is compared to both the Global Atmospheric Circulation Statistics (1963-1973) climatology and to the 1987 radiosonde climatology. The clear sky SAGE II climatology is found to be approximately half the level of both the clear/cloudy sky radiosonde climatologies. To determine whether this is realistic for these two different climatologies or includes additional observational and instrumental biases, we took the 1987 radiosonde data set and identified approximately 800 correlative profile pairs. The observational biases inherent to SAGE II and the radiosondes produce a set of profile pairs characteristic of clear sky, land conditions. A critical review of the radiosonde measurement capability was carried out to establish the operating range and accuracy in the upper troposphere. We show that even with tight coincidence criterion, the quality of the profile pair comparisons varies considerably because of strong water vapor variability occurring on small time and space scales. Annual zonal means calculated from the set of profile pairs again finds SAGE II significantly drier in many latitude bands. Resolving the radiosonde data base by hygrometer type shows this to be true for all hygrometers except for the thin film capacitive type (Vaisala Humicap). For this hygrometer, between 4.5 and 6.5 km SAGE II is drier by approximately 25.%, and from 8.5 to 11.5 km they are nearly equivalent when global annual means are compared. The good agreement with the Vaisala Humicap, currently the most accurate and responsive hygrometer in operational use, suggests existing radiosonde climatologies contain a significant moist bias in the upper troposphere.

  19. A comparison of the Stratospheric Aerosol and Gas Experiment II tropospheric water vapor to radiosonde measurements

    SciTech Connect

    Larsen, J.C.; Chiou, E.W. ); Chu, W.P.; McCormick, M.P.; McMaster, L.R. ); Oltmans, S. ); Rind, D. )

    1993-03-20

    Upper tropospheric Stratospheric Aerosol and Gas Experiment II (SAGE II) water vapor observations are compared to correlative radiosonde observations and radiosonde based climatologies. The SAGE II 1987 monthly zonal mean water vapor climatology is compared to both the Global Atmospheric Circulation Statistics (1963-1973) climatology and to the 1987 radiosonde climatology. The clear sky SAGE II climatology is found to be approximately half the level of both the clear/cloudy sky radiosonde climatologies. To determine whether this is realistic for these two different climatologies or includes additional observational and instrumental biases, the authors took the 1987 radiosonde data set and identified approximately 800 correlative profile pairs. The observational biases inherent to SAGE II and the radiosondes produce a set of profile pairs characteristic of clear sky, land conditions. A critical review of the radiosonde measurement capability was carried out to establish the operating range and accuracy in the upper troposphere. The authors show that even with tight coincidence criterion, the quality of the profile pair comparisons varies considerably because of strong water vapor variability occurring on small time and space scales. Annual zonal means calculated from the set of profile pairs again finds SAGE II significantly drier in many latitude bands. Resolving the radiosonde data base by hygrometer type shows this to be true for all hygrometers except for the thin film capacitive type (Vaisala Humicap). For this hygrometer, between 4.5 and 6.5 km SAGE II is drier by approximately 25.%, and from 8.5 to 11.5 km they are nearly equivalent when global annual means are compared. The good agreement with the Vaisala Humicap, currently the most accurate and responsive hygrometer in operational use, suggests existing radiosonde climatologies contain a significant moist bias in the upper troposphere. 31 refs., 16 figs., 6 tabs.

  20. CONTAIN assessment of the NUPEC mixing experiments. Supplement 1

    SciTech Connect

    Stamps, D.W.; Murata, K.K.

    1998-02-01

    In the original report (Reference 1), to which this report is a supplement, the results of CONTAIN code calculations were presented for five thermal-hydraulic experiments performed in the NUPEC 1/4-scale model containment, including the International Standard Problem ISP-35. In the original report, calculated helium concentrations were presented per NUPEC`s specifications for ISP-35. In contrast, this supplemental report presents the helium concentrations on a conventional dry basis, which is physically consistent with the gas chromatography data. These conventionally defined dry helium concentrations are compared with the previously reported results and are found to exhibit trends that are more consistent with measured data. While agreement between the predicted results and data is substantially improved in general for the M-8-1 experiment using these helium concentrations as opposed to the ISP-35 specifications, general improvement in agreement is not observed in all cases.

  1. On the Stratospheric Aerosol and Gas Experiment III on the International Space Station

    NASA Technical Reports Server (NTRS)

    Hernandez, Gloria; Zawodny, Joseph M.; Cisewski, Michael S.; Thornton, Brooke M.; Panetta, Andrew D,; Roell, Marilee M.; Vernier, Jean-Paul

    2014-01-01

    The Stratospheric Aerosol and Gas Experiment III on International Space Station (SAGE3/ISS) is anticipated to be delivered to Cape Canaveral in the spring of 2015. This is the fourth generation, fifth instrument, of visible/near-IR solar occultation instruments operated by the National Aeronautics and Space Agency (NASA) to investigate the Earth's upper atmosphere. The instrument is a moderate resolution spectrometer covering wavelengths from 290 nm to 1550 nm. The nominal science products include vertical profiles of trace gases, such as ozone, nitrogen dioxide and water vapor, along with multi-wavelength aerosol extinction. The SAGE3/ISS validation program will be based upon internal consistency of the measurements, detailed analysis of the retrieval algorithm, and comparisons with independent correlative measurements. The Instrument Payload (IP), mission architecture, and major challenges are also discussed.

  2. Aerosols, clouds, and precipitation in the North Atlantic trades observed during the Barbados aerosol cloud experiment - Part 1: Distributions and variability

    NASA Astrophysics Data System (ADS)

    Jung, Eunsil; Albrecht, Bruce A.; Feingold, Graham; Jonsson, Haflidi H.; Chuang, Patrick; Donaher, Shaunna L.

    2016-07-01

    Shallow marine cumulus clouds are by far the most frequently observed cloud type over the Earth's oceans; but they are poorly understood and have not been investigated as extensively as stratocumulus clouds. This study describes and discusses the properties and variations of aerosol, cloud, and precipitation associated with shallow marine cumulus clouds observed in the North Atlantic trades during a field campaign (Barbados Aerosol Cloud Experiment- BACEX, March-April 2010), which took place off Barbados where African dust periodically affects the region. The principal observing platform was the Center for Interdisciplinary Remotely Piloted Aircraft Studies (CIRPAS) Twin Otter (TO) research aircraft, which was equipped with standard meteorological instruments, a zenith pointing cloud radar and probes that measured aerosol, cloud, and precipitation characteristics.The temporal variation and vertical distribution of aerosols observed from the 15 flights, which included the most intense African dust event during all of 2010 in Barbados, showed a wide range of aerosol conditions. During dusty periods, aerosol concentrations increased substantially in the size range between 0.5 and 10 µm (diameter), particles that are large enough to be effective giant cloud condensation nuclei (CCN). The 10-day back trajectories showed three distinct air masses with distinct vertical structures associated with air masses originating in the Atlantic (typical maritime air mass with relatively low aerosol concentrations in the marine boundary layer), Africa (Saharan air layer), and mid-latitudes (continental pollution plumes). Despite the large differences in the total mass loading and the origin of the aerosols, the overall shapes of the aerosol particle size distributions were consistent, with the exception of the transition period.The TO was able to sample many clouds at various phases of growth. Maximum cloud depth observed was less than ˜ 3 km, while most clouds were less than 1 km

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

    NASA Technical Reports Server (NTRS)

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

    1995-01-01

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

  4. Physical and optical properties of mineral dust aerosol during the Dust and Biomass-burning Experiment

    NASA Astrophysics Data System (ADS)

    Osborne, S. R.; Johnson, B. T.; Haywood, J. M.; Baran, A. J.; Harrison, M. A. J.; McConnell, C. L.

    2008-12-01

    We present aircraft measurements of dust aerosol during the Dust and Biomass-burning Experiment (DABEX), a project affiliated with the African Monsoon Multidisciplinary Analysis. DABEX took place between 13 January and 3 February 2006 in Sahelian west Africa, with the aircraft based at Niamey, Niger. The data set is augmented with Aerosol Robotic Network (AERONET) data. A mineral dust layer below 1-2 km (sourced from the north) and an overlying biomass burning (BB) layer (sourced from anthropogenic fires to the south) was observed on all days, although variability was observed in both layers. There is evidence of ozone loss within the dust, but with CO levels between 140 and 170 ppbv some history of combustion has occurred. Size distribution of the dust is compared with that of the BB aerosol and with dust measured near Senegal, during the Dust Outflow and Deposition to the Ocean (DODO-1) experiment. For accurate representation of the optical properties, five log-normals to the size distribution across sizes 0.05-5 μm are required, although two log-normals are adequate. The single scattering albedo was almost purely scattering, with values of 0.99 ± 0.01. During the strongest dust events the dust contribution to the column optical depth was 75-80%, compared to a DABEX mean of 50%. The aircraft-derived optical depth varied between 0.19 and 1.07, with the dust-only contribution between 0.07 and 0.81. AERONET optical depth trends are in good agreement with aircraft during DABEX, albeit with a bias to higher aircraft values. Retrieved AERONET aerosol size distributions show variable agreement with the aircraft. Differences between Versions 1 and 2 of the AERONET algorithm are highlighted.

  5. Stability and aerosolization of pressurized metered dose inhalers containing thymopentin nanoparticles produced using a bottom-up process.

    PubMed

    Tan, Yinhe; Yang, Zhiwen; Pan, Xin; Chen, Meiwan; Feng, Min; Wang, Lili; Liu, Hu; Shan, Ziyun; Wu, Chuanbin

    2012-05-10

    The objective of this study was to investigate the stability and aerosolization of pressurized metered dose inhalers (pMDIs) containing thymopentin nanoparticles. Thymopentin nanoparticles, fabricated by a bottom-up process, were suspended in hydrofluoroalkane (HFA) 134a together with cineole and/or n-heptane to produce pMDI formulations. The stability study of the pMDIs obtained was carried out at ambient temperature for 6 months. The amount of thymopentin and the aerosolization properties of pMDIs were determined using high-performance liquid chromatography (HPLC) and a twin-stage impinger (TSI), respectively. Based on the results, thymopentin nanoparticles were readily suspended in HFA 134a with the aid of cineole and/or n-heptane to form physically stable pMDI formulations, and more than 98% of the labeled amount of thymopentin and over 50% of the fine particle fraction (FPF) of the pMDIs were achieved. During storage, it was found that for all pMDIs more than 97% of the labeled amount of thymopentin and FPF greater than 47% were achieved. Moreover, the size of thymopentin nanoparticles in propellant containing cineole and n-heptane showed little change. It is, therefore, concluded that the pMDIs comprising thymopentin nanoparticles developed in this study were stable and suitable for inhalation therapy for systemic action. PMID:22343132

  6. Overview of the Stratospheric Aerosol and Gas Experiment III (SAGE III) on the International Space Station

    NASA Astrophysics Data System (ADS)

    Flittner, David; Pitts, Michael; Zawodny, Joe; Hill, Charles; Damadeo, Robert; Moore, Randy; Cisewski, Michael

    2012-07-01

    The Stratospheric Aerosol and Gas Experiment (SAGE) III is the fourth generation of solar occultation instruments operated by NASA, the first coming under a different acronym, to investigate the Earth's upper atmosphere. Three flight-ready SAGE III instruments were built by Ball Aerospace in the late 1990s, with one launched aboard the former Russian Avaiation and Space Agency (now known as Roskosmos) Meteor-3M (M3M) platform on 10 December 2001 (continuing until the platform lost power in 2006). Another of the original instruments was manifested for the International Space Station (ISS) in the 2004 time frame, but was delayed because of budgetary considerations. Fortunately, that SAGE III/ISS mission was restarted in 2009 with a major focus upon filling an anticipated gap in ozone and aerosol observations in the second half of this decade. This exciting mission utilizes contributions from both the Science Mission Directorate and the Human Exploration and Operations Mission Directorate within the National Aeronautics and Space Administration and the European Space Agency to enable scientific measurements that will provide the basis for the analysis of five of the nine critical constituents identified in the U.S. National Plan for Stratospheric Monitoring. A related paper by Anderson et al. discusses the. Presented here is an overview of the mission architecture, its implementation and the data that will be produced by SAGE III/ISS, including their expected accuracy and coverage. The 52-degree inclined orbit of the ISS is well-suited for solar occultation and provides near-global observations on a monthly basis with excellent coverage of low and mid-latitudes. This is similar to that of the SAGE II mission (1985-2005), whose data set has served the international atmospheric science community as a standard for stratospheric ozone and aerosol measurements. The nominal science products include vertical profiles of trace gases, such as ozone, nitrogen dioxide and water

  7. Comparison of In Situ Aerosol Data from the ACE-Asia 2001 Experiment

    NASA Astrophysics Data System (ADS)

    Knobelspiesse, K. D.; Pietras, C.; Miller, M. A.; Reynolds, R. M.; Frouin, R.; Quinn, P. K.; Deschamps, P. Y.; Werdell, P. J.; Fargion, G. S.

    2002-05-01

    The Asian Pacific Regional Aerosol Characterization Experiment (ACE-Asia) is an international, multidisciplinary project to further knowledge about atmospheric aerosols. ACE-Asia included an intensive field measurement campaign during the spring of 2001 off the coasts of China, Japan and Korea. The Sensor Intercomparison and Merger for Biological and Interdisciplinary Oceanic Studies (SIMBIOS) Project participated in the ACE-Asia cruise of the R/V Ronald H. Brown, which departed from Hawaii on 2001/03/15, sailed west to the Sea of Japan, and finished in Yokosuka, Japan on 2001/04/19. The SIMBIOS Project compares and merges data projects from multiple ocean color missions. As In Situ data are essential for merger and comparison of satellite ocean color measurements, the Project is interested in instrumentation devopment and data base building. The SeaWiFS Bio-optical Archive and Storage System (SeaBASS) is the database used and maintained by the SIMBIOS project. The ACE-Asia cruise was an excellent opportunity to compare data from a variety of maritime sun photometers, as several aerosol conditions were experienced. These included low Aerosol Optical Thickness (AOT) maritime conditions near Hawaii and extremely high AOT dust conditions in the Sea of Japan. Concurrant measurements were made with the PREDE POM-01 Mark II radiometer, a Laboratoire d'Optique Atmosphérique (LOA) SIMBAD, a Laboratorie d'Optique Atmosphérique (LOA) SIMBAD-a, two Solar Light, Inc. Microtops II's, and Brookhaven National Laboratory's Fast Rotating Shadowband Radiometer (FRSR). In addition, a Micro Pulse Lidar (MPL) was deployed that provides vertical aerosol distributions. Data were processed utilizing new algorithms to screen errors due to improper pointing at the sun, a problem previously recognized for the Microtops II. Comparisons of AOT at 500nm and Angstrom Exponent were made for all the instruments. The hand held, direct solar sun photometers (Microtops II, SIMBAD and SIMBADa

  8. Stratospheric aerosol and gas experiments I and II comparisons with ozonesondes

    SciTech Connect

    Veiga, R.E.; Cunnold, D.M.; Chu, W.P.

    1995-05-20

    Ozone profiles measured by the Stratospheric Aerosol and Gas Experiments (SAGE) I and II are compared with ozonesonde profiles at 24 stations over the period extending from 1979 through 1991. Ozonesonde/satellite differences at 21 stations with SAGE II overpasses were computed down to 11.5 km in the midlatitudes, to 15.5 km in the lower latitudes, and for nine stations with SAGE I overpasses down to 15.5 km. The set of individual satellite and ozonesonde profile comparisons most closely colocated in time and space shows mean absolute differences relative to the satellite measurement of 6 {plus_minus} 2% for SAGE II and 8 {plus_minus}3% for SAGE I. The ensemble of ozonesonde/satellite differences, when averaged over all altitudes, shows that for SAGE II, 70% were less than 5%, whereas for SAGE I, 50% were less than 5%. The best agreement occurred in the altitude region near the ozone density maximum where almost all the relative differences were less than 5%. Most of the statistically significant differences occurred below the ozone maximum down to the tropopause in the region of steepest ozone gradients and typically ranged between 0 and {minus}20%. Correlations between ozone and aerosol extinction in the northern midlatitudes indicate that aerosols had no discernible impact on the ozonesonde/satellite differences and on the stratosphere during 1984 to mid-1991. 42 refs., 8 figs., 1 tab.

  9. Trace Gases and Aerosol in the Boundary Layer of the Northern Asia: TROICA Experiments

    NASA Astrophysics Data System (ADS)

    Elanksy, N. F.; Aloyan, A. E.; Berezina, E. V.; Elokhov, A. S.; Brenninkmeijer, C. A.; Kopeikin, V. M.; Moeseenko, K. B.; Lavrova, O. V.; Pankratova, N. V.; Safronov, A. N.; Shumsky, R. A.; Skorokhod, A. I.; Tarasova, O. A.; Vivchar, A. V.; Grisenko, A. M.

    2007-12-01

    The TROICA experiment (Transcontinental Observations Into the Chemistry of the Atmosphere) started in 1995. A mobile railroad laboratory is being used for measurements of atmospheric gases, aerosol, solar radiation and meteorological parameters. The laboratory wagon is directly coupled to the locomotive of a passenger train traveling along electrified railroads of Russia. Eleven expeditions have been conducted to the moment of which nine were performed along the Trans-Siberian railroad from Moscow to Vladivostok (around 9300 km). One expedition was North-South between Murmansk and Kislovodsk, and one was around the mega-city of Moscow. The huge coverage of the continental regions and the repetition of the expeditions provide unique information on processes controlling variability of the key trace gases (O3, NOx, CO, CO2, CH4, some VOCs) and aerosols with high temporal and spatial resolution over different scales from continental to local (hundreds meters). Multiple crossings of settlements allowed determining typical variations of surface gases and aerosol concentrations within cities and their plumes. 222Rn concentration data were used for estimates of CO, CH4 and CO2 nocturnal fluxes from the soil and vegetation. Impacts of different factors, like Western Siberian gas and oil industry, forest fires, transboundary air pollution transport and some other can be evaluated based on the measurement data by comparing them with results of model output and hence can be used for model validation. Emissions of the atmospheric CO and CH4 were studied in several expeditions using isotopes analysis.

  10. Stratospheric Aerosol and Gas Experiments 1 and 2: Comparisons with ozonesondes

    NASA Technical Reports Server (NTRS)

    Veiga, Robert E.; Cunnold, Derek M.; Chu, William P.; McCormick, M. Patrick

    1995-01-01

    Ozone profiles measured by the Stratospheric Aerosol and Gas Experiments (SAGE) 1 and 2 are compared with ozonesonde profiles at 24 stations over the period extending from 1979 through 1991. Ozonesonde/satellite differences at 21 stations with SAGE 2 overpasses were computed down to 11.5 km in midlatitudes, to 15.5 km in the lower latitudes, and for nine stations with SAGE 1 overpasses down to 15.5 km. The set of individual satellite and ozonesonde profile comparisons most closely colocated in time and space shows mean absolute differences relative to the satellite measurement of 6 +/- 2% for SAGE 2 and 8 +/- 3% for SAGE 1. The ensemble of ozonesonde/satellite differences, when averaged over all altitudes, shows that for SAGE 2, 70% were less than 5%, whereas for SAGE 1, 50% were less than 5%. The best agreement occurred in the altitude region near the ozone density maximum where almost all the relative differences were less than 5%. Most of the statistically significant differences occurred below the ozone maximum down to the tropopause in the region of steepest ozone gradients and typically ranged between 0 and -20%. Correlations between ozone and aerosol extinction in the northern midlatitudes indicate that aerosols had no discernible impact on the ozonesonde/satellite differences and on the SAGE 2 ozone retrieval for the levels of extinction encountered in the lower stratosphere during 1984 to mid-1991.

  11. Aerosol and cloud sensing with the lidar in-space technology experiment (LITE)

    NASA Astrophysics Data System (ADS)

    Winker, David M.; McCormick, Michael P.

    1994-12-01

    The Lidar In-space Technology Experiment (LITE) is a multi-wavelength backscatter lidar developed by NASA Langley Research Center to fly on the Space Shuttle. The LITE instrument is built around a three-wavelength Nd:YAG laser and a 1-meter diameter telescope. The laser operates at 10 Hz and produces about 500 mJ per pulse at 1064 nm and 532 nm, and 150 mJ per pulse at 355 nm. The objective of the LITE program is to develop the engineering processes required for space lidar and to demonstrate applications of space-based lidar to remote sensing of the atmosphere. The LITE instrument was designed to study a wide range of cloud and aerosol phenomena. To this end, a comprehensive program of scientific investigations has been planned for the upcoming mission. Simulations of on-orbit performance show the instrument has sufficient sensitivity to detect even thin cirrus on a single-shot basis. Signal averaging provides the capability of measuring the height and structure of the planetary boundary layer, aerosols in the free troposphere, the stratospheric aerosol layer, and density profiles to an altitude of 40 km. The instrument has successfully completed a ground-test phase and is scheduled to fly on the Space Shuttle Discovery for a 9- day mission in September 1994.

  12. Aerosol and cloud sensing with the Lidar In-space Technology Experiment (LITE)

    NASA Technical Reports Server (NTRS)

    Winker, D. M.; McCormick, M. P.

    1994-01-01

    The Lidar In-space Technology Experiment (LITE) is a multi-wavelength backscatter lidar developed by NASA Langley Research Center to fly on the Space Shuttle. The LITE instrument is built around a three-wavelength ND:YAG laser and a 1-meter diameter telescope. The laser operates at 10 Hz and produces about 500 mJ per pulse at 1064 nm and 532 nm, and 150 mJ per pulse at 355 nm. The objective of the LITE program is to develop the engineering processes required for space lidar and to demonstrate applications of space-based lidar to remote sensing of the atmosphere. The LITE instrument was designed to study a wide range of cloud and aerosol phenomena. To this end, a comprehensive program of scientific investigations has been planned for the upcoming mission. Simulations of on-orbit performance show the instrument has sufficient sensitivity to detect even thin cirrus on a single-shot basis. Signal averaging provides the capability of measuring the height and structure of the planetary boundary layer, aerosols in the free troposphere, the stratospheric aerosol layer, and density profiles to an altitude of 40 km. The instrument has successfully completed a ground-test phase and is scheduled to fly on the Space Shuttle Discovery for a 9-day mission in September 1994.

  13. Experiments probing the influence of air exchange rates on secondary organic aerosols derived from indoor chemistry

    NASA Astrophysics Data System (ADS)

    Weschler, Charles J.; Shields, Helen C.

    Reactions between ozone and terpenes have been shown to increase the concentrations of submicron particles in indoor settings. The present study was designed to examine the influence of air exchange rates on the concentrations of these secondary organic aerosols as well as on the evolution of their particle size distributions. The experiments were performed in a manipulated office setting containing a constant source of d-limonene and an ozone generator that was remotely turned "on" or "off" at 6 h intervals. The particle number concentrations were monitored using an optical particle counter with eight-channels ranging from 0.1-0.2 to>2.0 μm diameter. The air exchange rates during the experiments were either high (working hours) or low (non-working hours) and ranged from 1.6 to>12 h -1, with intermediate exchange rates. Given the emission rates of ozone and d-limonene used in these studies, at an air exchange rate of 1.6 h -1 particle number concentration in the 0.1-0.2 μm size-range peaked 1.2 h after the ozone generator was switched on. In the ensuing 4.8 h particle counts increased in successive size-ranges up to the 0.5-0.7 μm diameter range. At higher air exchange rates, the resulting concentrations of total particles and particle mass (calculated from particle counts) were smaller, and at exchange rates exceeding 12 h -1, no excess particle formation was detectable with the instrument used in this study. Particle size evolved through accretion and, in some cases, coagulation. There was evidence for coagulation among particles in the smallest size-range at low air exchange rates (high particle concentrations) but no evidence of coagulation was apparent at higher air exchange rates (lower particle concentrations). At higher air exchange rates the particle count or size distributions were shifted towards smaller particle diameters and less time was required to achieve the maximum concentration in each of the size-ranges where discernable particle growth

  14. Assessment of aerosol optical property and radiative effect for the layer decoupling cases over the northern South China Sea during the 7-SEAS/Dongsha Experiment

    NASA Astrophysics Data System (ADS)

    Pani, Shantanu Kumar; Wang, Sheng-Hsiang; Lin, Neng-Huei; Tsay, Si-Chee; Lolli, Simone; Chuang, Ming-Tung; Lee, Chung-Te; Chantara, Somporn; Yu, Jin-Yi

    2016-05-01

    The aerosol radiative effect can be modulated by the vertical distribution and optical properties of aerosols, particularly when aerosol layers are decoupled. Direct aerosol radiative effects over the northern South China Sea (SCS) were assessed by incorporating an observed data set of aerosol optical properties obtained from the Seven South East Asian Studies (7-SEAS)/Dongsha Experiment into a radiative transfer model. Aerosol optical properties for a two-layer structure of aerosol transport were estimated. In the radiative transfer calculations, aerosol variability (i.e., diversity of source region, aerosol type, and vertical distribution) for the complex aerosol environment was also carefully quantified. The column-integrated aerosol optical depth (AOD) at 500 nm was 0.1-0.3 for near-surface aerosols and increased 1-5 times in presence of upper layer biomass-burning aerosols. A case study showed the strong aerosol absorption (single-scattering albedo (ω) ≈ 0.92 at 440 nm wavelength) exhibited by the upper layer when associated with predominantly biomass-burning aerosols, and the ω (≈0.95) of near-surface aerosols was greater than that of the upper layer aerosols because of the presence of mixed type aerosols. The presence of upper level aerosol transport could enhance the radiative efficiency at the surface (i.e., cooling) and lower atmosphere (i.e., heating) by up to -13.7 and +9.6 W m-2 per AOD, respectively. Such enhancement could potentially modify atmospheric stability, can influence atmospheric circulation, as well as the hydrological cycle over the tropical and low-latitude marginal northern SCS.

  15. CalWater 2 - Precipitation, Aerosols, and Pacific Atmospheric Rivers Experiment

    NASA Astrophysics Data System (ADS)

    Spackman, J. R.; Ralph, F. M.; Prather, K. A.; Cayan, D. R.; DeMott, P. J.; Dettinger, M. D.; Fairall, C. W.; Leung, L. R.; Rosenfeld, D.; Rutledge, S. A.; Waliser, D. E.; White, A. B.

    2014-12-01

    Emerging research has identified two phenomena that play key roles in the variability of the water supply and the incidence of extreme precipitation events along the West Coast of the United States. These phenomena include the role of (1) atmospheric rivers (ARs) in delivering much of the precipitation associated with major storms along the U.S. West Coast, and (2) aerosols—from local sources as well as those transported from remote continents—and their modulating effects on western U.S. precipitation. A better understanding of these processes is needed to reduce uncertainties in weather predictions and climate projections of extreme precipitation and its effects, including the provision of beneficial water supply. This presentation summarizes the science objectives and strategies to address gaps associated with (1) the evolution and structure of ARs including cloud and precipitation processes and air-sea interaction, and (2) aerosol interaction with ARs and the impact on precipitation, including locally-generated aerosol effects on orographic precipitation along the U.S. West Coast. Observations are proposed for multiple winter seasons as part of a 5-year broad interagency vision referred to as CalWater 2 to address these science gaps (http://esrl.noaa.gov/psd/calwater). In January-February 2015, a field campaign has been planned consisting of a targeted set of aircraft and ship-based measurements and associated evaluation of data in near-shore regions of California and in the eastern Pacific. In close coordination with NOAA, DOE's Atmospheric Radiation Measurement (ARM) program is also contributing air and shipborne facilities for ACAPEX (ARM Cloud Aerosol and Precipitation Experiment), a DOE-sponsored study complementing CalWater 2. Ground-based measurements from NOAA's HydroMeteorological Testbed (HMT) network in California and aerosol chemical instrumentation at Bodega Bay, California have been designed to add important near surface-level context for the

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

    DOE Data Explorer

    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.

  17. Characterization of aerosol-containing chemical simulant clouds using a sensitive, thermal infrared imaging spectrometer

    NASA Astrophysics Data System (ADS)

    Hall, Jeffrey L.; D'Amico, Francis M.; Kolodzey, Steven J.; Qian, Jun; Polak, Mark L.; Westerberg, Karl; Chang, Clement S.

    2011-05-01

    A sensitive, ground-based thermal imaging spectrometer was deployed at the Army's Dugway Proving Ground to remotely monitor explosively released chemical-warfare-agent-simulant clouds from stand-off ranges of a few kilometers. The sensor has 128 spectral bands covering the 7.6 to 13.5 micron region. The measured cloud spectra clearly showed scattering of high-elevation-angle sky radiance by liquid aerosols or dust in the clouds: we present arguments that show why the scattering is most likely due to dust. This observation has significant implications for early detection of dust-laden chemical clouds. On one hand, detection algorithms must properly account for the scattered radiation component, which would include out-of-scene radiation components as well as a dust signature; on the other hand, this scattering gives rise to an enhanced "delta-T" for detection by a ground-based sensor.

  18. IRES-Containing VEEV Vaccine Protects Cynomolgus Macaques from IE Venezuelan Equine Encephalitis Virus Aerosol Challenge

    PubMed Central

    Rossi, Shannan L.; Russell-Lodrigue, Kasi E.; Killeen, Stephanie Z.; Wang, Eryu; Leal, Grace; Bergren, Nicholas A.; Vinet-Oliphant, Heather; Weaver, Scott C.; Roy, Chad J.

    2015-01-01

    Venezuelan equine encephalitis virus (VEEV) is an arbovirus endemic to the Americas that is responsible for severe, sometimes fatal, disease in humans and horses. We previously described an IRES-based VEE vaccine candidate based up the IE serotype that offers complete protection against a lethal subtype IE VEEV challenge in mice. Here we demonstrate the IRES-based vaccine’s ability to protect against febrile disease in cynomolgus macaques. Vaccination was well tolerated and elicited robust neutralizing antibody titers noticed as early as day 14. Moreover, complete protection from disease characterized by absence of viremia and characteristic fever following aerosolized IE VEEV challenge was observed in all vaccinees compared to control animals, which developed clinical disease. Together, these results highlight the safety and efficacy of IRES-based VEEV vaccine to protect against an endemic, pathogenic VEEV IE serotype. PMID:26020513

  19. Eastern Pacific Emitted Aerosol Cloud Experiment (E-PEACE) 2011: Design and Highlights

    NASA Astrophysics Data System (ADS)

    Russell, L. M.; Sorooshian, A.; Seinfeld, J.; Albrecht, B. A.; Nenes, A.; Ahlm, L.; Chen, Y.; Craven, J. S.; Coggon, M.; Frossard, A. A.; Jung, E.; Lin, J. J.; Metcalf, A. R.; Modini, R.; Muelmenstaedt, J.; Shingler, T.; Song, S.; Wang, Z.; Wonaschuetz, A.

    2011-12-01

    Aerosol-cloud-radiation interactions are widely held to be the largest single source of uncertainty in climate model projections of future climate change due to increasing anthropogenic emissions. The underlying causes of this uncertainty among modeled predictions of climate are the gaps in our fundamental understanding of cloud processes. There has been significant progress with both observations and models on these important questions. However, while the qualitative aspects of the indirect effects of aerosols on clouds are well known, the quantitative representation of these processes is nontrivial and limits our ability to represent them in global climate models. The Eastern Pacific Emitted Aerosol Cloud Experiment (E-PEACE) 2011 was a targeted aircraft campaign with embedded modeling studies, using the Center for Interdisciplinary Remotely-Piloted Aircraft Studies (CIRPAS) Twin Otter aircraft and the R/V Point Sur in July 2011 off the coast of Monterey, California, with a full payload of instruments to measure particle and cloud number, mass, composition, and water uptake distributions. To date, the global models lack (i) accurate aerosol particle activation, with the resulting implications for the profiles of supersaturation, vertical velocity, liquid water content, and drop distribution; (ii) realistic microphysical growth and precipitation processes that control the formation and impacts of drizzle on cloud structure, lifetime, and particle concentration; and (iii) eddy-based transport processes that control the effects of entrainment on cloud thickness and lifetime as well as the dispersion of aerosol plumes. These are basic scientific issues that have not been addressed by climate models or by geoengineering proposals that involve perturbing marine stratocumulus. In this talk, we summarize three central aspects of the collaborative E-PEACE design and the resulting highlights: 1. Controlled particle sources were used to separate particle-induced feedbacks

  20. Aerosol and cloud chemistry of amines from CCS - reactivity experiments and numerical modeling

    NASA Astrophysics Data System (ADS)

    Weller, Christian; Tilgner, Andreas; Herrmann, Hartmut

    2013-04-01

    Capturing CO2 from the exhaust of power plants using amine scrubbing is a common technology. Therefore, amines can be released during the carbon capture process. To investigate the tropospheric chemical fate of amines from CO2 capturing processes and their oxidation products, the impact of aqueous aerosol particles and cloud droplets on the amine chemistry has been considered. Aqueous phase reactivity experiments of NO3 radicals and ozone with relevant amines and their corresponding nitrosamines were performed. Furthermore, nitrosamine formation and nitrosamine photolysis was investigated during laboratory experiments. These experiments implicated that aqueous phase photolysis can be an effective sink for nitrosamines and that ozone is unreactive towards amines and nitrosamines. Multiphase phase oxidation schemes of amines, nitrosamines and amides were developed, coupled to the existing multiphase chemistry mechanism CAPRAM and built into the Lagrangian parcel model SPACCIM using published and newly measured data. As a result, both deliquescent particles and cloud droplets are important compartments for the multiphase processing of amines and their products. Amines can be readily oxidised by OH radicals in the gas and cloud phase during daytime summer conditions. However, amine oxidation is restricted during winter conditions with low photochemical activity leading to long lifetimes of amines. The importance of the gas and aqueous phase depends strongly on the partitioning of the different amines. Furthermore, the simulations revealed that the aqueous formation of nitrosamines in aerosol particles and could droplets is not a relevant process under tropospheric conditions.

  1. Real time analysis of lead-containing atmospheric particles in Beijing during springtime by single particle aerosol mass spectrometry.

    PubMed

    Ma, Li; Li, Mei; Huang, Zhengxu; Li, Lei; Gao, Wei; Nian, Huiqing; Zou, Lilin; Fu, Zhong; Gao, Jian; Chai, Fahe; Zhou, Zhen

    2016-07-01

    Using a single particle aerosol mass spectrometer (SPAMS), the chemical composition and size distributions of lead (Pb)-containing particles with diameter from 0.1 μm to 2.0 μm in Beijing were analyzed in the spring of 2011 during clear, hazy, and dusty days. Based on mass spectral features of particles, cluster analysis was applied to Pb-containing particles, and six major classes were acquired consisting of K-rich, carboneous, Fe-rich, dust, Pb-rich, and Cl-rich particles. Pb-containing particles accounted for 4.2-5.3%, 21.8-22.7%, and 3.2% of total particle number during clear, hazy and dusty days, respectively. K-rich particles are a major contribution to Pb-containing particles, varying from 30.8% to 82.1% of total number of Pb-containing particles, lowest during dusty days and highest during hazy days. The results reflect that the chemical composition and amount of Pb-containing particles has been affected by meteorological conditions as well as the emissions of natural and anthropogenic sources. K-rich particles and carbonaceous particles could be mainly assigned to the emissions of coal combustion. Other classes of Pb-containing particles may be associated with metallurgical processes, coal combustion, dust, and waste incineration etc. In addition, Pb-containing particles during dusty days were first time studied by SPAMS. This method could provide a powerful tool for monitoring and controlling of Pb pollution in real time. PMID:27085059

  2. Reactive uptake of N2O5 by aerosols containing dicarboxylic acids. Effect of particle phase, composition, and nitrate content.

    PubMed

    Griffiths, Paul T; Badger, Claire L; Cox, R Anthony; Folkers, Mareike; Henk, Hartmut H; Mentel, Thomas F

    2009-04-30

    Reactive uptake coefficients for loss of N(2)O(5) to micron-size aerosols containing oxalic malonic, succinic, and glutaric acids, and mixtures with ammonium hydrogen sulfate and ammonium sulfate, are presented. The uptake measurements were made using two different systems: atmospheric pressure laminar flow tube reactor (Cambridge) and the Large Indoor Aerosol Chamber at Forschungszentrum Juelich. Generally good agreement is observed for the data recorded using the two techniques. Measured uptake coefficients lie in the range 5 x 10(-4)-3 x 10(-2), dependent on relative humidity, on particle phase, and on particle composition. Uptake to solid particles is generally slow, with observed uptake coefficients less than 1 x 10(-3), while uptake to liquid particles is around an order of magnitude more efficient. These results are rationalized using a numerical model employing explicit treatment of both transport and chemistry. Our results indicate a modest effect of the dicarboxylic acids on uptake and confirm the strong effect of particle phase, liquid water content, and particulate nitrate concentrations. PMID:19385680

  3. SPEAM-II experiment for the measurement of stratospheric NO2, O3 and aerosols

    NASA Technical Reports Server (NTRS)

    Mcelroy, C. T.; Mcarthur, L. J. B.; Kerr, J. B.; Wardle, D. I.; Tarasick, D.; Midwinter, C.

    1994-01-01

    Following the success of the Sunphotometer Earth Atmosphere Measurement (SPEAM-I) experiment, a more involved experiment was developed to fly as part of the second set of Canadian Experiments (CANEX-2) which will fly on the US Space Shuttle in the fall of 1992. The instrument complement includes an IBM-PC compatible control computer, a hand-held diode array spectrophotometer, and an interference-filter, limb imaging radiometer for the measurement of the atmospheric airglow. The hand-held spectrometer will measure nitrogen dioxide, ozone and aerosols. The limb imaging radiometer will observe emissions from the O2(1 DELTA) and O2(1 SIGMA) airglow bands. Only the spectrophotometer will be discussed here.

  4. The THS Experiment: Ex Situ Analyses of Titan's Aerosol Analogs Produced at Low Temperature (200K)

    NASA Astrophysics Data System (ADS)

    Sciamma-O'Brien, E. M.; Upton, K. T.; Beauchamp, J. L.; Salama, F.

    2014-12-01

    In the study presented here, we used the COSmIC/Titan Haze Simulation (THS) experiment, an experimental platform developed to study Titan's atmospheric chemistry at low temperature, to produce aerosols representative of the early stages of Titan's aerosol formation. In the THS, the chemistry is simulated by plasma in the stream of a supersonic expansion. With this unique design, the gas is jet-cooled to Titan-like temperature (~150K) before inducing the chemistry by plasma, and remains at low temperature in the plasma discharge (~200K). Because of the pulsed nature of the plasma, the residence time of the gas in the discharge is only a few microseconds, which leads to a truncated chemistry and allows for the study of the first and intermediate steps of the chemistry. Different N2-CH4-based gas mixtures can be injected in the plasma, with or without the addition of heavier precursors present as trace elements on Titan, in order to monitor the evolution of the chemical growth. Both the gas phase and solid phase products resulting from the plasma-induced chemistry can be monitored and analyzed using a combination of complementary in situ and ex situ diagnostics. In a recently published study, a mass spectrometry analysis of the gas phase has demonstrated that the THS is a unique tool to probe the first and intermediate steps of Titan's atmospheric chemistry at Titan-like temperature. In particular, the mass spectra obtained in a N2-CH4-C2H2-C6H6 mixture are relevant for comparison to Cassini's CAPS-IBS instrument. Here we present the results of a complementary study of the solid phase. Scanning Electron Microscopy images have shown that aggregates produced in N2-CH4-C2H2-C6H6 mixtures are much larger (up to 5 μm in diameter) than those produced in N2-CH4 mixtures (0.1-0.5 μm). Direct Analysis in Real Time mass spectrometry (DART-MS) combined with Collision Induced Dissociation (CID) have detected the presence of aminoacetonitrile, a precursor of glycine, in the THS

  5. Horizontal variability of aerosol optical properties observed during the ARCTAS airborne experiment

    NASA Astrophysics Data System (ADS)

    Shinozuka, Y.; Redemann, J.; Russell, P. B.; Livingston, J. M.; Clarke, A. D.; Podolske, J. R.

    2010-12-01

    The properties of tropospheric aerosol and gas vary within a satellite grid cell and between ground-based instruments. This hinders comparison between satellite and suborbital measurements of different spatial scales as well as their applications to climate and air quality studies. This paper quantifies the realistic range of the variability in aerosol optical depth (AOD), its Angstrom exponent, in-situ extinction coefficient and carbon monoxide mixing ratio over horizontal distances of 1-30 km, using measurements from the ARCTAS airborne experiment. The Canada phase in June and July 2008, in which smoke from local forest fires was sampled, likely represents the most heterogeneous of the ambient aerosol environments common over the globe. The relative standard deviation (stdrel) of AOD measured with the 14-channel Ames Airborne Tracking Sunphotometer (AATS-14) has median 19.4% (at 499 nm) among thousands of horizontal 20 km segments. For 6 km segments the analogous median is 9.1%. Another measure of horizontal variability, the autocorrelation (r) of AOD499 across 20 km and 6 km segments is 0.37 and 0.71, respectively. In contrast, the Alaska phase in April 2008, which sampled particles transported from Asia, is presumably among the most homogeneous environments. The median stdrel is 3.0% and r is 0.90, both over 30 km, only slightly different from those for 1 km (stdrel=0.4% and r=1.00). r in the Canada phase is ~0.2 less for in situ extinction coefficient (from a nephelometer and a particle soot absorption photometer) than for the AOD. It is ~0.1 less than for the carbon monoxide mixing ratio. The trends of horizontal variability with distance and aerosol environment are different for the wavelength dependence and the humidity response of light scattering. We discuss challenges in estimating aerosol optical properties, particle size and chemical composition from measurements at a distant location. The statistical parameters thus help interpret existing remote

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

    NASA Astrophysics Data System (ADS)

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

    2016-01-01

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

  7. Inference of stratospheric aerosol composition and size distribution from SAGE II satellite measurements

    NASA Technical Reports Server (NTRS)

    Wang, Pi-Huan; Mccormick, M. P.; Fuller, W. H.; Yue, G. K.; Swissler, T. J.; Osborn, M. T.

    1989-01-01

    A method for inferring stratospheric aerosol composition and size distribution from the water vapor concentration and aerosol extinction measurements obtained in the Stratospheric Aerosol and Gas Experiment (SAGE) II and the associated temperature from the NMC. The aerosols are assumed to be sulfuric acid-water droplets. A modified Levenberg-Marquardt algorithm is used to determine model size distribution parameters based on the SAGE II multiwavelength aerosol extinctions. It is found that the best aerosol size information is contained in the aerosol radius range between about 0.25 and 0.80 micron.

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

    NASA Astrophysics Data System (ADS)

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

    2015-07-01

    The Chemistry-Aerosol Mediterranean Experiment (ChArMEx; http://charmex.lsce.ipsl.fr) is a collaborative research program federating international activities to investigate Mediterranean regional chemistry-climate interactions. A special observing period (SOP-1a) including intensive airborne measurements was performed in the framework of the Aerosol Direct Radiative Forcing on the Mediterranean Climate (ADRIMED) project during the Mediterranean dry season over the western and central Mediterranean basins, with a focus on aerosol-radiation measurements and their modeling. The SOP-1a took place from 11 June to 5 July 2013. Airborne measurements were made by both the ATR-42 and F-20 French research aircraft operated from Sardinia (Italy) and instrumented for in situ and remote-sensing measurements, respectively, and by sounding and drifting balloons, launched in Minorca. The experimental set-up also involved several ground-based measurement sites on islands including two ground-based reference stations in Corsica and Lampedusa and secondary monitoring sites in Minorca and Sicily. Additional measurements including lidar profiling were also performed on alert during aircraft operations at EARLINET/ACTRIS stations at Granada and Barcelona in Spain, and in southern Italy. Remote sensing aerosol products from satellites (MSG/SEVIRI, MODIS) and from the AERONET/PHOTONS network were also used. Dedicated meso-scale and regional modelling experiments were performed in relation to this observational effort. We provide here an overview of the different surface and aircraft observations deployed during the ChArMEx/ADRIMED period and of associated modeling studies together with an analysis of the synoptic conditions that determined the aerosol emission and transport. Meteorological conditions observed during this campaign (moderate temperatures and southern flows) were not favorable to produce high level of atmospheric pollutants nor

  9. Comparison of Stratospheric Aerosol and Gas Experiment II and balloon-borne stratospheric water vapor measurements

    NASA Technical Reports Server (NTRS)

    Pruvost, P.; Ovarlez, J.; Lenoble, J.; Chu, W. P.

    1993-01-01

    The Stratospheric Aerosol and Gas Experiment II has one channel at 940 nm related to water vapor. Two inversion procedures were developed independently in order to obtain the water vapor profile: the Chahine method by the Langley Research Center, and the Mill method by the Laboratoire d'Optique Atmospherique. Comparisons were made between these two algorithms and some results are presented at midlatitudes (about 45 deg N) and tropical latitudes (12-25 deg S). They are compared with in situ frost point hygrometer data provided by balloon experiments from the Laboratoire de Meteorologie Dynamique. At +/- 0.5 ppmv, agreement between the inversion results and the experimental results was obtained in the altitude range from 18-19 to 26-27 km. Below 18-19 km and above 26-27 km the error is larger (sometimes 1 ppmv and more).

  10. Comparison of Stratospheric Aerosol and Gas Experiment II and balloon-borne stratospheric water vapor measurements

    SciTech Connect

    Pruvost, P.; Lenoble, J. ); Ovarlez, J. ); Chu, W.P. )

    1993-03-20

    The Stratospheric Aerosol and Gas Experiment II has one channel at 940 nm related to water vapor. Two inversion procedures were developed independently in order to obtain the water vapor profile: the Chahine method by the Langley Research Center, and the Mill method by the Laboratoire d'Optique Atmospherique. Comparisons were made between these two algorithms and some results are presented at mid-latitudes ([approximately]45[degrees]N) and tropical latitudes (12[degrees]S-25[degrees]S). They are compared with in situ frost point hygrometer data provided by balloon experiments from the Laboratoire de Meteorologie Dynamique. At [plus minus]0.5 ppmv, agreement between the inversion results and the experimental results was obtained in the altitude range from 18-19 to 26-27 km. Below 18-19 km and above 26-27 km the error is larger (sometimes 1 ppmv and more). 17 refs., 4 figs.

  11. Comparison of Stratospheric Aerosol and Gas Experiment II and balloon-borne stratospheric water vapor measurements

    NASA Astrophysics Data System (ADS)

    Pruvost, P.; Ovarlez, J.; Lenoble, J.; Chu, W. P.

    1993-03-01

    The Stratospheric Aerosol and Gas Experiment II has one channel at 940 nm related to water vapor. Two inversion procedures were developed independently in order to obtain the water vapor profile: the Chahine method by the Langley Research center, and the Mill method by the Laboratoire d'Optique Atmosphérique. Comparisons were made between these two algorithms and some results are presented at mid-latitudes (~45°N) and tropical latitudes (12°S-25°S). They are compared with in situ frost point hygrometer data provided by balloon experiments from the Laboratoire de Météorologie Dynamique. At +/-0.5 ppmv, agreement between the inversion results and the experimental results was obtained in the altitude range from 18-19 to 26-27 km. Below 18-19 km and above 26-27 km the error is larger (sometimes 1 ppmv and more).

  12. Observations of Ozone and Aerosols Over Mexico and Gulf of Mexico During INTEX- B/MILAGRO Field Experiment

    NASA Astrophysics Data System (ADS)

    Butler, C. F.; Browell, E. V.; Hair, J. W.; Fenn, M. A.; Notari, A.; Kooi, S. A.; Ismail, S.; Avery, M. A.; Pierce, R. B.

    2007-12-01

    The NASA Langley Research Center's Differential Absorption Lidar (LaRC/DIAL) system has been used to measure ozone and aerosol distributions in many airborne global tropospheric and stratospheric campaigns since 1980. The tropospheric configuration of this system was flown on the NASA DC-8 during the INTEX-B (Phase-I)/MILAGRO (I/M) field experiment, which was conducted from 24 February to 22 March 2006 over Mexico and the Gulf of Mexico. DIAL remote profile measurements were made from near the surface to above the tropopause along the flight track of the DC-8 with a small data void region of 750 m above and below the aircraft. Aerosol scattering ratios were determined at two wavelengths for a gross estimation of the relative size of the observed particles and measurements of aerosol depolarization were made to distinguish nonspherical aerosols, such as dust and some aerosols in aged fire plumes. In situ measurements of ozone from the FASTOZ instrument on the DC-8 were used to constrain the interpolation of the nadir and zenith ozone lidar measurements, which then provided an estimate of the entire tropospheric ozone profile along the flight track. A first order correction for aerosol attenuation was made to the aerosol profiles by using an assumed extinction-to- backscatter ratio to better characterize the attenuation by thick aerosol layers. The DIAL system was used to determine the large-scale variability and context of air masses being sampled in situ on the DC-8 and to direct the in situ sampling strategy in real time. Plumes from biomass burning in southern Mexico were often observed in the free troposphere over the Gulf of Mexico and over eastern Mexico. The Mexico City (MC) pollution plume was readily apparent with high ozone (>100 ppbv), high aerosol scattering (S>20), and enhanced aerosol depolarization (D>10%). The top of the MC pollution extended to a depth of about 2.5 km AGL. Some observations showed the MC plume spilling out over the mountains to

  13. Initial operation and checkout of stratospheric aerosol gas experiment and Meteor-3M satellite

    NASA Astrophysics Data System (ADS)

    Habib, Shahid; Makridenko, Leonid; Chu, William P.; Salikhov, Rashid; Moore, Alvah S., Jr.; Trepte, Charles R.; Cisewski, Michael S.

    2003-04-01

    Under a joint agreement between the National Aeronautics and Space Agency (NASA) and the Russian Aviation and Space Agency (RASA), the Stratospheric Aerosol Gas Experiment III (SAGE III) instrument was launched in low earth orbit on December 10, 2001 aboard the Russian Meteor-3M(1) satellite from the Baikonur Cosmodrome. SAGE III is a spectrometer that measures attenuated radiation in the 282 nm to 1550 nm wavelength range to obtain the vertical profiles of ozone, aerosols, and other chemical species that are critical in studying the trends for the global climate change phenomena. This instrument version is more advanced than any of the previous versions and has more spectral bands, elaborate data gathering and storage, and intelligent terrestrial software. There are a number of Russian scientific instruments aboard the Meteor satellite in addition to the SAGE III instrument. These instruments deal with land imaging and biomass changes, hydro-meteorological monitoring, and helio-geophysical research. This mission was under development for over a period of six years and offered a number of unique technical and program management challenges for both Agencies. SAGE III has a long space heritage, and four earlier versions of this instrument have flown in space for nearly two decades now. In fact, SAGE II, the fourth instrument, is still flying in space on NASA's Earth Radiation Budget Satellite (ERBS), and has been providing important atmospheric data over the last 18 years. It has provided vital ozone and aerosol data in the mid latitudes and has contributed vastly in ozone depletion research. Ball Aerospace built the instrument under Langley Research Center's (LaRC) management. This paper presents the process and approach deployed by the SAGE III and the Meteor teams in performing the initial on-orbit checkout. It further documents a number of early science results obtained by deploying low risk, carefully coordinated procedures in resolving the serious operational

  14. Initial Operation and Checkout of Stratospheric Aerosol Gas Experiment and Meteor-3M Satellite

    NASA Technical Reports Server (NTRS)

    Habib, Shahid; Makridenko, L.; Chu, W.; Salikhov, R.; Moore, A.; Trepte, C.; Cisewski, M.

    2002-01-01

    Under a joint agreement between the National Aeronautics and Space Agency (NASA) and the Russian Aviation and Space Agency (RASA), the Stratospheric Aerosol Gas Experiment III (SAGE III) instrument was launched in low earth orbit on December 10,2001 aboard the Russian Meteor-3M satellite from the Baikonur Cosmodrome. SAGE III is a spectrometer that measures attenuated radiation in the 282 nm to 1550 nm wavelength range to obtain the vertical profiles of ozone, aerosols, and other chemical species that are critical in studying the trends for the global climate change phenomena. This instrument version is more advanced than any of the previous versions and has more spectral bands, elaborate data gathering and storage, and intelligent terrestrial software. There are a number of Russian scientific instruments aboard the Meteor satellite in addition to the SAGE III instrument. These instruments deal with land imaging and biomass changes, hydro-meteorological monitoring, and helio-geophysical research. This mission was under development for over a period of six years and offered a number of unique technical and program management challenges for both Agencies. SAGE III has a long space heritage, and four earlier versions of this instrument have flown in space for nearly two decades now. In fact, SAGE II, the fourth instrument, is still flying in space on NASA s Earth Radiation Budget Satellite (ERBS), and has been providing important atmospheric data over the last 18 years. It has provided vital ozone and aerosol data in the mid latitudes and has contributed vastly in ozone depletion research. Ball Aerospace built the instrument under Langley Research Center s (LaRC) management. This paper presents innovative approaches deployed by the SAGE III and the Meteor teams in performing the initial on-orbit checkout. It further documents a number of early science results obtained by deploying low risk, carefully coordinated procedures in resolving the serious operational issues

  15. Experiments on aerosol-induced cooling in the nocturnal boundary layer

    NASA Astrophysics Data System (ADS)

    Sreenivas, K.; Singh, D. K.; Vk, P.; Mukund, V.; Subramanian, G.

    2012-12-01

    In the nocturnal boundary layer (NBL), under calm & clear-sky conditions, radiation is the principal mode of heat transfer & it determines the temperature distribution close to the ground. Radiative processes thus influence the surface energy budget, & play a decisive role in many micro-meteorological processes including the formation of radiation-fog & inversion layer. Here, we report hyper-cooling of air layers close to the ground that has a radiative origin. Resulting vertical temperature distribution has an anomalous profile with an elevated minimum few decimetres above the ground (known as Lifted Temperature Minimum; LTM). Even though the first observation of this type of profile dates back to 1930s, its origin has not been explained till recently. We report field experiments to elucidate effects of emissivity and other physical properties of the ground on the LTM profile. Field observations clearly indicate that LTM-profiles are observed as a rule in the lowest meter of the NBL. We also demonstrate that the air-layer near the ground, rather than the ground itself, leads the post sunset cooling. This fact changes the very nature of the sensible heat-flux boundary condition. A laboratory experimental setup has been developed that can reproduce LTM. Lab-experiments demonstrate that the high cooling rates observed in the field experiments arise from the presence of aerosols & the intensity of cooling is proportional to aerosol concentration (Fig-1). We have also captured penetrative convection cells in the field experiments (Fig-2). Results presented here thus help in parameterizing transport processes in the NBL.

  16. Inversion of solar extinction data from the Apollo-Soyuz Test Project Stratospheric Aerosol Measurement (ASTP/SAM) experiment

    NASA Technical Reports Server (NTRS)

    Pepin, T. J.

    1977-01-01

    The inversion methods are reported that have been used to determine the vertical profile of the extinction coefficient due to the stratospheric aerosols from data measured during the ASTP/SAM solar occultation experiment. Inversion methods include the onion skin peel technique and methods of solving the Fredholm equation for the problem subject to smoothing constraints. The latter of these approaches involves a double inversion scheme. Comparisons are made between the inverted results from the SAM experiment and near simultaneous measurements made by lidar and balloon born dustsonde. The results are used to demonstrate the assumptions required to perform the inversions for aerosols.

  17. Stratospheric aerosol and gas experiment III (SAGE III) aerosol and trace gas measurements for Earth Observing System (EOS)

    NASA Technical Reports Server (NTRS)

    Mccormick, M. P.; Chu, W. P.; Zawodny, J. M.; Mauldin, L. E.; Mcmaster, L. R.

    1991-01-01

    The SAGE III instrument, the latest in a series of satellite-based instruments employing the self-calibrating solar occultation technique to monitor aerosols and trace gases in the atmosphere, and potential contributions to monitoring global change and other EOS objectives are described. Uses of these data are illustrated with SAGE I and II long-term ozone, aerosol, and water vapor data. The SAGE III instrument will improve the SAM II and SAGE data products with greater overall accuracy, and will provide the ability to extend these measurements over a greater height range. SAGE III will provide long-term self-calibrating global data sets from the midtroposphere to mesosphere, which will contribute greatly to the quantification and understanding of global change.

  18. Linking variations in sea spray aerosol particle hygroscopicity to composition during two microcosm experiments

    NASA Astrophysics Data System (ADS)

    Forestieri, Sara D.; Cornwell, Gavin C.; Helgestad, Taylor M.; Moore, Kathryn A.; Lee, Christopher; Novak, Gordon A.; Sultana, Camille M.; Wang, Xiaofei; Bertram, Timothy H.; Prather, Kimberly A.; Cappa, Christopher D.

    2016-07-01

    The extent to which water uptake influences the light scattering ability of marine sea spray aerosol (SSA) particles depends critically on SSA chemical composition. The organic fraction of SSA can increase during phytoplankton blooms, decreasing the salt content and therefore the hygroscopicity of the particles. In this study, subsaturated hygroscopic growth factors at 85 % relative humidity (GF(85 %)) of predominately submicron SSA particles were quantified during two induced phytoplankton blooms in marine aerosol reference tanks (MARTs). One MART was illuminated with fluorescent lights and the other was illuminated with sunlight, referred to as the "indoor" and "outdoor" MARTs, respectively. Optically weighted GF(85 %) values for SSA particles were derived from measurements of light scattering and particle size distributions. The mean optically weighted SSA diameters were 530 and 570 nm for the indoor and outdoor MARTs, respectively. The GF(85 %) measurements were made concurrently with online particle composition measurements, including bulk composition (using an Aerodyne high-resolution aerosol mass spectrometer) and single particle (using an aerosol time-of-flight mass spectrometer) measurement, and a variety of water-composition measurements. During both microcosm experiments, the observed optically weighted GF(85 %) values were depressed substantially relative to pure inorganic sea salt by 5 to 15 %. There was also a time lag between GF(85 %) depression and the peak chlorophyll a (Chl a) concentrations by either 1 (indoor MART) or 3-to-6 (outdoor MART) days. The fraction of organic matter in the SSA particles generally increased after the Chl a peaked, also with a time lag, and ranged from about 0.25 to 0.5 by volume. The observed depression in the GF(85 %) values (relative to pure sea salt) is consistent with the large observed volume fractions of non-refractory organic matter (NR-OM) comprising the SSA. The GF(85 %) values exhibited a reasonable negative

  19. CalWater 2 - Precipitation, Aerosols, and Pacific Atmospheric Rivers Experiment

    NASA Astrophysics Data System (ADS)

    Spackman, Ryan; Ralph, Marty; Prather, Kim; Cayan, Dan; DeMott, Paul; Dettinger, Mike; Fairall, Chris; Leung, Ruby; Rosenfeld, Daniel; Rutledge, Steven; Waliser, Duane; White, Allen

    2014-05-01

    Emerging research has identified two phenomena that play key roles in the variability of the water supply and the incidence of extreme precipitation events along the West Coast of the United States. These phenomena include the role of (1) atmospheric rivers (ARs) in delivering much of the precipitation associated with major storms along the U.S. West Coast, and (2) aerosols—from local sources as well as those transported from remote continents—and their modulating effects on western U.S. precipitation. A better understanding of these processes is needed to reduce uncertainties in weather predictions and climate projections of extreme precipitation and its effects, including the provision of beneficial water supply. This presentation summarizes science gaps associated with (1) the evolution and structure of ARs including cloud and precipitation processes and air-sea interaction, and (2) aerosol interaction with ARs and the impact on precipitation, including locally-generated aerosol effects on orographic precipitation along the U.S. West Coast. Observations are proposed for multiple winter seasons as part of a 5-year broad interagency vision referred to as CalWater 2 to address these science gaps (http://esrl.noaa.gov/psd/calwater). In the near term, a science investigation is being planned including a targeted set of aircraft and ship-based measurements and associated evaluation of data in near-shore regions of California and in the eastern Pacific for an intensive observing period between January 2015 and March 2015. DOE's Atmospheric Radiation Measurement (ARM) program and NOAA are coordinating on deployment of airborne and ship-borne facilities for this period in a DOE-sponsored study called ACAPEX (ARM Cloud Aerosol and Precipitation Experiment) to complement CalWater 2. The motivation for this major study is based on findings that have emerged in the last few years from airborne and ground-based studies including CalWater and NOAA's HydroMeterology Testbed

  20. Lidar Observations of Tropospheric Aerosols Over Northeastern South Africa During the ARREX and SAFARI-2000 Dry Season Experiments

    NASA Technical Reports Server (NTRS)

    Campbell, James R.; Welton, Ellsworth J.; Spinhirne, James D.; Ji, Qiang; Tsay, Si-Chee; Piketh, Stuart J.; Barenbrug, Marguerite; Holben, Brent; Starr, David OC. (Technical Monitor)

    2002-01-01

    During the ARREX-1999 and SAFARI-2000 Dry Season experiments a micropulse lidar (523 nm) instrument was operated at the Skukuza Airport in northeastern South Africa. The Mar was collocated with a diverse array of passive radiometric equipment. For SAFARI-2000 the processed Mar data yields a daytime time-series of layer mean/derived aerosol optical properties, including extinction-to-backscatter ratios and vertical extinction cross-section profile. Combined with 523 run aerosol optical depth and spectral Angstrom exponent calculations from available CIMEL sun-photometer data and normalized broadband flux measurements the temporal evolution of the near surface aerosol layer optical properties is analyzed for climatological trends. For the densest smoke/haze events the extinction-to-backscatter ratio is found to be between 60-80/sr, and corresponding Angstrom exponent calculations near and above 1.75. The optical characteristics of an evolving smoke event from SAFARI-2000 are extensively detailed. The advecting smoke was embedded within two distinct stratified thermodynamic layers, causing the particulate mass to advect over the instrument array in an incoherent manner on the afternoon of its occurrence. Surface broadband flux forcing due to the smoke is calculated, as is the evolution in the vertical aerosol extinction profile as measured by the Han Finally, observations of persistent elevated aerosol during ARREX-1999 are presented and discussed. The lack of corroborating observations the following year makes these observation; both unique and noteworthy in the scope of regional aerosol transport over southern Africa.

  1. The VOCALS Regional Experiment: Aerosol-Cloud-Precipitation Interactions in Marine Boundary Layer Cloud

    NASA Astrophysics Data System (ADS)

    Wood, R.

    2012-12-01

    Robert Wood, C.S. Bretherton, C. R. Mechoso, R. A. Weller, B. J. Huebert, H. Coe, B. A. Albrecht, P. H. Daum, D. Leon, A. Clarke, P. Zuidema, C. W. Fairall, G. Allen, S. deSzoeke, G. Feingold, J. Kazil, S. Yuter, R. George, A. Berner, C. Terai, G. Painter, H. Wang, M. Wyant, D. Mechem The VAMOS Ocean-Cloud-Atmosphere-Land Study Regional Experiment (VOCALS-REx) is an international field program designed to make observations of poorly understood but critical components of the coupled climate system of the southeast Pacific (SEP), a region dominated by strong coastal upwelling, extensive cold SSTs, and home to the largest subtropical stratocumulus deck on Earth. VOCALS-REx took place during October and November 2008 and involved five research aircraft, two ships and two surface sites in northen Chile. A central theme of VOCALS-REx is the improved understanding of links between aerosols, clouds and precipitation and their impacts on marine stratocumulus radiative properties. In this presentation, we will present a synthesis of results from VOCALS-REx focusing on the following questions: (a) how are aerosols, clouds and precipitation inter-related in the SEP region? (b) what microphysical-macrophysical interactions are necessary for the formation and maintenance of open cells? (c) how do cloud and MBL properties change across the strong microphysical gradients from the South American coast to the remote ocean?

  2. The Borexino solar neutrino experiment and its scintillator containment vessel

    NASA Astrophysics Data System (ADS)

    Cadonati, Laura

    2001-05-01

    Thirty years ago, the first solar neutrino detector proved fusion reactions power the Sun. However, the total rate detected in this and all subsequent solar neutrino experiments is consistently two to three times lower than predicted by the Standard Solar Model. Current experiments seek to explain this ``solar neutrino puzzle'' through non-standard particle properties, like neutrino mass and flavor mixing, within the context of the MSW theory. The detection of the monoenergetic 7Be solar neutrino is the missing clue for the solution of the solar neutrino problem; this constitutes the main physics goal of Borexino, a real- time, high-statistics solar neutrino detector located under the Gran Sasso mountain, in Italy. In the first part of this thesis, I present a Monte Carlo study of the expected performance of Borexino, with simulations of the neutrino rate, the external y background and the α/β/γ activity in the scintillator. The Standard Solar Model predicts a solar neutrino rate of about 60 events/day in Borexino in the 0.25-0.8 MeV window, mostly due to 7Be neutrinos. Given the design scintillator radiopurity levels (10-16 g/g 238U and 232Th and 10-14 g/g K), Borexino will detect such a rate with a ~2.4% statistical error, after one year. In the MSW Small (Large) Angle scenario, the predicted rate of ~13 (33) events/day will be detected with 8% (4%) error. The sensitivity of Borexino to 8B and pp neutrinos and to a Galactic supernova event is also discussed. The second part of this dissertation is devoted to the liquid scintillator containment vessel, an 8.5 m diameter sphere built of bonded panels of 0.125 mm polymer film. Through an extensive materials testing program we have identified an amorphous nylon-6 film which meets all the critical requirements for the success of Borexino. I describe tests of tensile strength, measurements of 222Rn diffusion through thin nylon films and of optical clarity. I discuss how the materials' radiopurity and mechanical

  3. Microanalysis of the aerosol collected over south-central New Mexico during the alive field experiment, May-December 1989

    NASA Astrophysics Data System (ADS)

    Sheridan, Patrick J.; Schnell, Russel C.; Kahl, Jonathan D.; Boatman, Joe F.; Garvey, Dennis M.

    Thirty-eight size-segregated aerosol samples were collected in the lower troposphere over the high desert of south-central New Mexico, using cascade impactors mounted onboard two research aircraft. Four of these samples were collected in early May, sixteen in mid-July, and the remaining ones in December 1989, during three segments of the ALIVE field initiative. Analytical electron microscope analyses of aerosol deposits and individual particles from these samples were performed to physically and chemically characterize the major particulate species present in the aerosol. Air-mass trajectories arriving at the sampling area in the May program were quite different from those calculated for the July period. In general, the May trajectories showed strong westerly winds, while the July winds were weaker and southerly, consistently passing over or very near the border cities of El Paso, Texas, and Ciudad Juarez, Mexico. Aerosol samples collected during the May period were predominantly fine (0.1-0.5 μm dia.), liquid H 2SO 4 droplets. Samples from the July experiment were comprised mostly of fine, solid (NH 4) 2SO 4 or mostly neutralized sulfate particles. In both sampling periods, numerous other particle classes were observed, including many types with probable terrestrial or anthropogenic sources. The numbers of these particles, however, were small when compared with the sulfates. Composite particle types, including sulfate/crustal and sulfate/carbonaceous, were also found to be present. The major differences in aerosol composition between the May and July samples (i.e. the extensive neutralization of sulfates in the July samples) can be explained by considering the different aerosol transport pathways and the proximity of the July aerosol to the El Paso/Juarez urban plume. Winds during the December experiment were quite variable, and may have contributed to the widely varying aerosol compositions observed in these samples. When the aircraft sampled the El Paso

  4. Micropulse lidar observations of tropospheric aerosols over northeastern South Africa during the ARREX and SAFARI 2000 dry season experiments

    NASA Astrophysics Data System (ADS)

    Campbell, James R.; Welton, Ellsworth J.; Spinhirne, James D.; Ji, Qiang; Tsay, Si-Chee; Piketh, Stuart J.; Barenbrug, Marguerite; Holben, Brent N.

    2003-07-01

    During the Aerosol Recirculation and Rainfall Experiment (ARREX 1999) and Southern African Regional Science Initiative (SAFARI 2000) dry season experiments, a micropulse lidar (523 nm) instrument was operated at the Skukuza Airport in northeastern South Africa. The lidar was colocated with a diverse array of passive radiometric equipment. For SAFARI 2000, a daytime time series of layer mean aerosol optical properties, including layer mean extinction-to-backscatter ratios and vertical extinction cross-section profiles are derived from the synthesis of the lidar data and aerosol optical depths from available AERONET Sun photometer data. Combined with derived spectral Angstrom exponents, normalized broadband flux measurements, and calculated air mass back-trajectories, the temporal evolution of the surface aerosol layer optical properties is analyzed for climatological trends. For dense biomass smoke events the extinction-to-backscatter ratio is between 50 and 90 sr, and corresponding spectral Angstrom exponent values are between 1.50 and 2.00. Observations of an advecting smoke event during SAFARI 2000 are shown. The smoke was embedded within two distinct stratified thermodynamic layers causing the particulate mass to advect over the instrument array in an incoherent manner on the afternoon of 1 September 2000. Significant surface broadband flux forcing of over -50 W/m2 was measured in this event. The evolution of the vertical aerosol extinction profile is profiled using the lidar data. Finally, observations of persistent elevated aerosol layers during ARREX 1999 are presented and discussed. Back-trajectory analyses combined with lidar and Sun photometer measurements indicate the likelihood for these aerosols being the result of long-range particulate transport from the southern and central South America.

  5. Individual aerosol particles in and below clouds along a Mt. Fuji slope: Modification of sea-salt-containing particles by in-cloud processing

    NASA Astrophysics Data System (ADS)

    Ueda, S.; Hirose, Y.; Miura, K.; Okochi, H.

    2014-02-01

    Sizes and compositions of atmospheric aerosol particles can be altered by in-cloud processing by absorption/adsorption of gaseous and particulate materials and drying of aerosol particles that were formerly activated as cloud condensation nuclei. To elucidate differences of aerosol particles before and after in-cloud processing, aerosols were observed along a slope of Mt. Fuji, Japan (3776 m a.s.l.) during the summer in 2011 and 2012 using a portable laser particle counter (LPC) and an aerosol sampler. Aerosol samples for analyses of elemental compositions were obtained using a cascade impactor at top-of-cloud, in-cloud, and below-cloud altitudes. To investigate composition changes via in-cloud processing, individual particles (0.5-2 μm diameter) of samples from five cases (days) collected at different altitudes under similar backward air mass trajectory conditions were analyzed using a transmission electron microscope (TEM) equipped with an energy dispersive X-ray analyzer. For most cases (four cases), most particles at all altitudes mainly comprised sea salts: mainly Na with some S and/or Cl. Of those, in two cases, sea-salt-containing particles with Cl were found in below-cloud samples, although sea-salt-containing particles in top-of-cloud samples did not contain Cl. This result suggests that Cl in the sea salt was displaced by other cloud components. In the other two cases, sea-salt-containing particles on samples at all altitudes were without Cl. However, molar ratios of S to Na (S/Na) of the sea-salt-containing particles of top-of-cloud samples were higher than those of below-cloud samples, suggesting that sulfuric acid or sulfate was added to sea-salt-containing particles after complete displacement of Cl by absorption of SO2 or coagulation with sulfate. The additional volume of sulfuric acid in clouds for the two cases was estimated using the observed S/Na values of sea-salt-containing particles. The estimation revealed that size changes by in

  6. A comparison of the Stratospheric Aerosol and Gas Experiment II tropospheric water vapor to radiosonde measurements

    NASA Technical Reports Server (NTRS)

    Larsen, J. C.; Chiou, E. W.; Chu, W. P.; Mccormick, M. P.; Mcmaster, L. R.; Oltmans, S.; Rind, D.

    1993-01-01

    Results are presented of a comparison beteen observations of the upper-tropospheric water vapor data obtained from the Stratospheric Aerosol and Gas Experiment II (SAGE II) instrument and radiosonde observations for 1987 and radiosonde-based climatologies. Colocated SAGE II-radiosonde measurement pairs are compared individually and in a zonal mean sense. A straight comparison of monthly zonal means between SAGE II and radiosondes for 1987 and Global Atmospheric Statistics (1963-1973) indicates that the clear-sky SAGE II climatology is approximately half the level of clear/cloudy sky of both radiosonde climatologies. Annual zonal means calculated from the set of profile pairs again showed SAGE II to be significantly drier in many altitude bands.

  7. The enhanced aerosol performance of salbutamol from dry powders containing engineered mannitol as excipient.

    PubMed

    Kaialy, Waseem; Martin, Gary P; Ticehurst, Martyn D; Momin, Mohammed N; Nokhodchi, Ali

    2010-06-15

    The aim of the present study was to investigate the effect of crystallising mannitol from different binary mixtures of acetone/water on the resultant physical properties and to determine the effects of any changes on in vitro aerosolisation performance, when the different mannitol crystals were used as a carrier in dry powder inhaler formulations containing salbutamol sulphate. Mannitol particles were crystallised under controlled conditions by dissolving the sugar in water and precipitating the sugar using binary mixtures of acetone/water in different percentages as anti-solvent media. For comparison purposes the physical properties and deposition behaviour of commercially available mannitol were also studied. SEM showed that all crystallised mannitol particles were more elongated than the commercial mannitol. Solid state studies revealed that commercial mannitol and mannitol crystallised using acetone in the presence of 10-25% v/v water as anti-solvent was beta-polymorphic form whereas mannitol crystallised in the presence of a small amount of water (0-7.5%) was the alpha-form. All the crystallised mannitol samples showed poor flowability. Nevertheless, the powdered crystallised mannitol and commercial samples were blended with salbutamol in the ratio 67.5:1. The aerosolisation performance of the formulations containing the engineered mannitol (evaluated using Multi Stage Liquid Impinger) was considerably better than that of the commercial mannitol formulation (the fine particle fraction was increased from 15.42% to 33.07-43.99%, for the formulations containing crystallised mannitol). Generally, carriers having a high tapped density and high fraction of fine carrier particles produced a high FPF. The improvement in the DPI performance could be attributed to the presence of elongated carrier particles with smooth surfaces since these are believed to have less adhesive forces between carrier and the drug resulting in easier detachment of the drug during the

  8. Inference of the aerosol Angstrom coefficient from SAGE short-wavelength data. [Stratospheric Aerosol and Gas Experiment

    NASA Technical Reports Server (NTRS)

    Lenoble, J.; Pruvost, P.

    1983-01-01

    SAGE four-channel transmission profiles are inverted to retrieve the extinction profiles from which the aerosol Angstrom coefficient alpha is obtained. The procedure allows one to check the influence of the NO2 absorption profile, which is small below 25 km. The results compare well with those obtained by a completely different procedure at NASA Langley Research Center, and the main features of the alpha profiles seem to be significant, even considering the rather large error bars. The relation between the retrieved Angstrom coefficient, the particle effective radius and the asymmetry factor is considered.

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

    NASA Astrophysics Data System (ADS)

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

    2016-01-01

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

  10. The Beijing Olympics as a Field Experiment - The Aerosol Footprint of a Megacity

    NASA Astrophysics Data System (ADS)

    Cermak, J.; Knutti, R.

    2009-04-01

    During the 2008 Olympic Summer Games, emission reductions were enforced in and around Beijing to improve the notoriously poor air quality in the city. In this presentation we explore the effect of these measures on the regional aerosol load. To this end, we compare satellite-retrieved aerosol optical thickness of that period with previous years. In addition to absolute changes we explore the 2008 situation in its meteorological context. Using a neural network approach we predict summer 2008 aerosol based on meteorological conditions. Predicted values are contrasted with observations. A statistically significant reduction of aerosol load is found in Beijing that decreases in magnitude and significance with increasing region size. Locally, the aerosol load (log(AOT)) was about 10-15% below the levels expected for the prevailing meteorological situation. The small size of this effect highlights the importance of regional aerosol transport.

  11. SAGE ground truth plan: Correlative measurements for the Stratospheric Aerosol and Gas Experiment (SAGE) on the AEM-B satellite

    NASA Technical Reports Server (NTRS)

    Russell, P. B. (Editor); Cunnold, D. M.; Grams, G. W.; Laver, J.; Mccormick, M. P.; Mcmaster, L. R.; Murcray, D. G.; Pepin, T. J.; Perry, T. W.; Planet, W. G.

    1979-01-01

    The ground truth plan is outlined for correlative measurements to validate the Stratospheric Aerosol and Gas Experiment (SAGE) sensor data. SAGE will fly aboard the Applications Explorer Mission-B satellite scheduled for launch in early 1979 and measure stratospheric vertical profiles of aerosol, ozone, nitrogen dioxide, and molecular extinction between 79 N and 79 S. latitude. The plan gives details of the location and times for the simultaneous satellite/correlative measurements for the nominal launch time, the rationale and choice of the correlative sensors, their characteristics and expected accuracies, and the conversion of their data to extinction profiles. In addition, an overview of the SAGE expected instrument performance and data inversion results are presented. Various atmospheric models representative of stratospheric aerosols and ozone are used in the SAGE and correlative sensor analyses.

  12. Ozone and aerosol distributions measured by airborne lidar during the 1988 Arctic Boundary Layer Experiment

    NASA Technical Reports Server (NTRS)

    Browell, Edward V.; Butler, Carolyn F.; Kooi, Susan A.

    1991-01-01

    Consideration is given to O3 and aerosol distributions measured from an aircraft using a DIAL system in order to study the sources and sinks of gases and aerosols over the tundra regions of Alaska during summer 1988. The tropospheric O3 budget over the Arctic was found to be strongly influenced by stratospheric intrusions. Regions of low aerosol scattering and enhanced O3 mixing ratios were usually correlated with descending air from the upper troposphere or lower stratosphere.

  13. Light absorption and morphological properties of soot-containing aerosols observed at an East Asian outflow site, Noto Peninsula, Japan

    NASA Astrophysics Data System (ADS)

    Ueda, Sayako; Nakayama, Tomoki; Taketani, Fumikazu; Adachi, Kouji; Matsuki, Atsushi; Iwamoto, Yoko; Sadanaga, Yasuhiro; Matsumi, Yutaka

    2016-03-01

    The coating of black carbon (BC) with inorganic salts and organic compounds can enhance the magnitude of light absorption by BC. To elucidate the enhancement of light absorption of aged BC particles and its relation to the mixing state and morphology of individual particles, we conducted observations of particles at an Asian outflow site in Noto Peninsula, Japan, in the spring of 2013. Absorption and scattering coefficients at 405, 532, and 781 nm and mass concentrations/mixing states of refractory BC in PM2.5 were measured using a three-wavelength photoacoustic soot spectrometer and a single-particle soot photometer (SP2), respectively, after passage through a thermodenuder (TD) maintained at 300 or 400 °C or a bypass line maintained at room temperature (25 °C). The average enhancement factor of BC light absorption due to coating was estimated by comparing absorption coefficients at 781 nm for particles that with and without passing through the TD at 300 °C and was found to be 1.22. The largest enhancements (> 1.30) were observed under high absorption coefficient periods when the air mass was long-range transported from urban areas in China. Aerosol samples were also analyzed using a transmission electron microscope (TEM) equipped with an energy dispersive X-ray analyzer. The morphological features and mixing states of soot-containing particles of four samples collected during the high absorption events were analyzed by comparing microphotographs before and after the evaporation of beam-sensitive materials by irradiation with a high-density electron beam. The majority of the soot in all samples was found as mixed particles with sulfate-containing spherules or as clusters of such spherules. For samples showing high enhancement (> 1.30) of BC light absorption, the TEM showed that the internally mixed soot-containing particles tended to have a more spherical shape and to be thickly coated. The SP2 measurements also suggested that the proportion of thickly coated

  14. Retrieval of composition and size distribution of stratospheric aerosols with the SAGE II satellite experiment

    NASA Technical Reports Server (NTRS)

    Yue, Glenn K.; Mccormick, M. P.; Chu, W. P.

    1986-01-01

    The SAGE II satellite system was launched on October 5, 1984. It has seven radiometric channels and is beginning to provide water vapor, NO2, and O3 concentration profiles and aerosol extinction profiles at a minimum of three wavelengths. A simple, fast and operational method of retrieving characteristics of stratospheric aerosols from the water vapor and three-wavelength aerosol extinction profiles is proposed. Some examples are given to show the practicality of the scheme. Possible sources of error for the retrieved values and the limitation of the proposed method are discussed. This method may also prove applicable to the study of aerosol characteristics in other multispectral extinction measurements.

  15. Phase transitions and hygroscopic growth of aerosol particles containing humic acid and mixtures of humic acid and ammonium sulphate

    NASA Astrophysics Data System (ADS)

    Badger, C. L.; George, I.; Griffiths, P. T.; Braban, C. F.; Cox, R. A.; Abbatt, J. P. D.

    2006-03-01

    The phase transitions and hygroscopic growth of two humic acid aerosols (Aldrich sodium salt and Leonardite Standard (IHSS)) and their mixtures with ammonium sulphate have been investigated using a combination of two techniques, Fourier transform infra-red (FTIR) spectroscopy and tandem differential mobility analysis (TDMA). A growth factor of 1.16 at 85% relative humidity (RH) was found for the Aldrich humic acid which can be regarded as an upper limit for growth factors of humic-like substances (HULIS) found in atmospheric aerosol and is significantly smaller than that of typical atmospheric inorganics. We find that the humic acid aerosols exhibit water uptake over all relative humidities with no apparent phase changes, suggesting that these aerosols readily form supersaturated droplets. In the mixed particles, the humic acid component decreases the deliquescence relative humidity (DRH) and increases the efflorescence relative humidity (ERH) of the ammonium sulphate component, and there is some degree of water uptake prior to ammonium sulphate deliquescence. In addition, at low RH, the FTIR spectra show that the ammonium is present in a different chemical environment in the mixed aerosols than in crystalline ammonium sulphate, perhaps existing as a complex with the humic materials. The growth factors of the mixed aerosols are intermediate between those of the single-component aerosols and can be predicted assuming that the inorganic and organic fractions take up water independently.

  16. Phase transitions and hygroscopic growth of aerosol particles containing humic acid and mixtures of humic acid and ammonium sulphate

    NASA Astrophysics Data System (ADS)

    Badger, C. L.; George, I.; Griffiths, P. T.; Braban, C. F.; Cox, R. A.; Abbatt, J. P. D.

    2005-10-01

    The phase transitions and hygroscopic growth of two humic acid aerosols (Aldrich sodium salt and Leonardite Standard (IHSS)) and their mixtures with ammonium sulphate have been investigated using a combination of two techniques, Fourier transform infra-red (FTIR) spectroscopy and tandem differential mobility analysis (TDMA). A growth factor of 1.16 at 85% relative humdity (RH) was found for the Aldrich humic acid which can be regarded as an upper limit for growth factors of humic-like substances (HULIS) found in atmospheric aerosol and is significantly smaller than that of typical atmospheric inorganics. We find that the humic acid aerosols exhibit water uptake over all relative humidites with no apparent phase changes, suggesting that these aerosols readily form supersaturated droplets. In the mixed particles, the humic acid component decreases the deliquescence relative humidity (DRH) and increases the efflorescence relative humidity (ERH) of the ammonium sulphate component, and there is some degree of water uptake prior to ammonium sulphate deliquescence. In addition, at low RH, the FTIR spectra show that the ammonium is present in a different chemical environment in the mixed aerosols than in crystalline ammonium sulphate, perhaps existing as a complex with the humic materials. The growth factors of the mixed aerosols are intermediate between those of the single component aerosols and can be predicted assuming that the inorganic and organic fractions take up water independently.

  17. The FLAME Deluge: organic aerosol emission ratios from combustion chamber experiments

    NASA Astrophysics Data System (ADS)

    Jolleys, Matthew; Coe, Hugh; McFiggans, Gordon; McMeeking, Gavin; Lee, Taehyoung; Sullivan, Amy; Kreidenweis, Sonia; Collett, Jeff

    2014-05-01

    A high level of variability has been identified amongst organic aerosol (OA) emission ratios (ER) from biomass burning (BB) under ambient conditions. However, it is difficult to assess the influences of potential drivers for this variability, given the wide range of conditions associated with wildfire measurements. Chamber experiments performed under controlled conditions provide a means of examining the effects of different fuel types and combustion conditions on OA emissions from biomass fuels. ERs have been characterised for 67 burns during the second Fire Laboratory at Missoula Experiment (FLAME II), involving 19 different species from 6 fuel types widely consumed in BB events in the US each year. Average normalised dOA/dCO ratios show a high degree of variability, both between and within different fuel types and species, typically exceeding variability between separate plumes in ambient measurements. Relationships with source conditions were found to be complex, with little consistent influence from fuel properties and combustion conditions for the entire range of experiments. No strong correlation across all fires was observed between dOA/dCO and modified combustion efficiency (MCE), which is used as an indicator of the proportional contributions of flaming and smouldering combustion phases throughout each burn. However, a negative correlation exists between dOA/dCO and MCE for some coniferous species, most notably Douglas fir, for which there is also an apparent influence from fuel moisture content. Significant contrasts were also identified between combustion emissions from different fuel components of additional coniferous species. Changes in fire efficiency were also shown to dramatically alter emissions for fires with very similar initial conditions. Although the relationship with MCE is variable between species, there is greater consistency with the level of oxygenation in OA. The ratio of the m/z 44 fragment to total OA mass concentration (f44) as

  18. Light absorption and morphological properties of soot-containing aerosols observed at an East Asian outflow site, Noto Peninsula, Japan

    NASA Astrophysics Data System (ADS)

    Ueda, S.; Nakayama, T.; Taketani, F.; Adachi, K.; Matsuki, A.; Iwamoto, Y.; Sadanaga, Y.; Matsumi, Y.

    2015-09-01

    The coating of black carbon (BC) with inorganic salts and organic compounds can enhance the magnitude of light absorption by BC. To elucidate the enhancement of light absorption of aged BC particles and its relation to the mixing state and morphology of individual particles, we conducted observations of particles at an Asian outflow site in Noto Peninsula, Japan, in the spring of 2013. Absorption and scattering coefficients at 405, 532, and 781 nm and mass concentrations/mixing states of refractory-BC in PM2.5 were measured using a three-wavelength photoacoustic soot spectrometer and a single-particle soot photometer (SP2), respectively, after passage through a heater maintained at 300 or 400 °C or a bypass line maintained at room temperature (25 °C). The average enhancement of BC light absorption due to coating was estimated by comparing absorption coefficients at 781 nm for particles that with and without passing through the heater and was found to be 22-23 %. The largest enhancements (> 30 %) were observed under high absorption coefficient conditions when the air mass was long-range transported from urban areas in China. Aerosol samples were also analyzed using a transmission electron microscope (TEM) equipped with an energy dispersive X-ray analyzer. The morphological features and mixing states of soot-containing particles of four samples collected during the high absorption coefficient events were analyzed by comparing microphotographs before and after the evaporation of beam-sensitive materials by irradiation with a high density electron beam. The majority of the soot in all samples was found as mixed particles with spherical sulfate or as clusters of sulfate spherules. For samples showing high enhancement (> 30 %) of BC light absorption, TEM showed that the internally mixed soot-containing particles tended to have a more spherical shape and to be embedded into the sulfate. The SP2 measurements also suggested that the proportion of thickly-coated soot was

  19. Aerosol source attributions and source-receptor relationships across the Northern Hemisphere ---- initial results from HTAP2 model experiments

    NASA Astrophysics Data System (ADS)

    Bian, H.; Chin, M.; Kucsera, T. L.; Torres, O.; Pan, X.

    2014-12-01

    Emissions and long-range transport of air pollution pose major concerns on air quality and climate change. To better assess the impact of intercontinental transport of air pollution on regional and global air quality, ecosystems, and near-term climate change, the UN Task Force on Hemispheric Transport of Air Pollution (HTAP) is organizing a phase II activity (HTAP2) that includes global and regional model experiments and data analysis, focusing on ozone and aerosols. This study presents the initial results of HTAP2 global aerosol modeling experiments. We will (a) evaluate the model results with surface and aircraft measurements, (b) examine the relative contributions of regional emission and extra-regional source on surface PM concentrations and column aerosol optical depth (AOD) over several NH pollution and dust source regions and the Arctic, and (c) quantify the source-receptor relationships in the pollution regions that reflect the sensitivity of regional aerosol amount to the regional and extra-regional emission reductions.

  20. Aerosol and nucleation research in support of NASA cloud physics experiments in space. [ice nuclei generator for the atmospheric cloud physics laboratory on Spacelab

    NASA Technical Reports Server (NTRS)

    Vali, G.; Rogers, D.; Gordon, G.; Saunders, C. P. R.; Reischel, M.; Black, R.

    1978-01-01

    Tasks performed in the development of an ice nucleus generator which, within the facility concept of the ACPL, would provide a test aerosol suitable for a large number and variety of potential experiments are described. The impact of Atmospheric Cloud Physics Laboratory scientific functional requirements on ice nuclei generation and characterization subsystems was established. Potential aerosol generating systems were evaluated with special emphasis on reliability, repeatability and general suitability for application in Spacelab. Possible contamination problems associated with aerosol generation techniques were examined. The ice nucleating abilities of candidate test aerosols were examined and the possible impact of impurities on the nucleating abilities of those aerosols were assessed as well as the relative merits of various methods of aerosol size and number density measurements.

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

    NASA Astrophysics Data System (ADS)

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

    2015-07-01

    The Chemistry-Aerosol Mediterranean Experiment (ChArMEx; http://charmex.lsce.ipsl.fr) is a collaborative research program federating international activities to investigate Mediterranean regional chemistry-climate interactions. A special observing period (SOP-1a) including intensive airborne measurements was performed in the framework of the Aerosol Direct Radiative Forcing on the Mediterranean Climate (ADRIMED) project during the Mediterranean dry season over the western and central Mediterranean basins, with a focus on aerosol-radiation measurements and their modeling. The SOP-1a took place from 11 June to 5 July 2013. Airborne measurements were made by both the ATR-42 and F-20 French research aircraft operated from Sardinia (Italy) and instrumented for in situ and remote-sensing measurements, respectively, and by sounding and drifting balloons, launched in Minorca. The experimental set-up also involved several ground-based measurement sites on islands including two ground-based reference stations in Corsica and Lampedusa and secondary monitoring sites in Minorca and Sicily. Additional measurements including lidar profiling were also performed on alert during aircraft operations at EARLINET/ACTRIS stations at Granada and Barcelona in Spain, and in southern Italy. Remote sensing aerosol products from satellites (MSG/SEVIRI, MODIS) and from the AERONET/PHOTONS network were also used. Dedicated meso-scale and regional modelling experiments were performed in relation to this observational effort. We provide here an overview of the different surface and aircraft observations deployed during the ChArMEx/ADRIMED period and of associated modeling studies together with an analysis of the synoptic conditions that determined the aerosol emission and transport. Meteorological conditions observed during this campaign (moderate temperatures and southern flows) were not favorable to produce high level of atmospheric pollutants nor

  2. An overview of the Chemistry-Aerosol Mediterranean Experiment (ChArMEx)

    NASA Astrophysics Data System (ADS)

    Dulac, François

    2014-05-01

    The Chemistry-Aerosol Mediterranean Experiment (ChArMEx, http://charmex.lsce.ipsl.fr) is a French initiative of the MISTRALS meta-programme (Mediterranean Integrated Studies at Regional And Locals Scales, http://www.mistrals-home.org). It federates a great number of national and international cooperative research actions aiming at a scientific assessment of the present and future state of the atmospheric environment in the Mediterranean Basin, and of its impacts on the regional climate, air quality, and marine biogeochemistry. The target is short-lived particulate and gaseous tropospheric trace species which are the cause of poor air quality events, have two-way interactions with climate, or impact the marine biogeochemistry, in a context of strong regional anthropogenic and climatic pressures. The six ChArMEx work packages include Emissions, Chemical processes and ageing, Transport processes and air quality, Aerosol-radiation-climate interactions, Deposition, and Present and future variability and trends. For several years, efforts have been deployed in several countries to develop (i) a network of relevant stations for atmospheric chemistry at background sites on islands and continental coasts around the basin and (ii) several intensive field campaigns including the operation of surface supersites and various instrumented mobile platforms (large and ultra-light aircraft, sounding and drifting balloons, ZeroCO2 sailboat). This presentation is an attempt to provide an overview of the various experimental, remote sensing and modelling efforts produced and to highlight major findings, by referencing more detailed ChArMEx presentations given in this conference and recently published or submitted papers. During the first phase of the project experimental efforts have been mainly concentrated on the western basin. Plans for the 2nd phase of ChArMEx, more dedicated towards the eastern basin, will also be given. In particular we plan to develop monitoring activities at

  3. The COSmIC/THS experiment: gas and solid phase studies of Titan aerosol simulants produced at cold temperature

    NASA Astrophysics Data System (ADS)

    Sciamma-OBrien, E. M.; Upton, K.; Beauchamp, J. L.; Salama, F.

    2013-12-01

    In Titan's atmosphere, a complex chemistry between N2 and CH4 occurs at temperatures lower than 200K and leads to the production of heavy molecules and subsequently solid aerosols that form the haze surrounding Titan. The Titan Haze Simulation (THS) experiment has been developed at the NASA Ames COSmIC facility to study Titan's atmospheric chemistry at low temperature, and in particular to study the chemical pathways that link the simple molecules resulting from the first steps of the N2-CH4 chemistry to benzene, and to PAHs and nitrogen-containing PAHs (PANHs), potential precursors to Titan's solid aerosols. In the COSmIC/THS, the chemistry is simulated by plasma in the stream of a supersonic expansion. With this unique design, the gas is jet-cooled to Titan-like temperature (~150K) before inducing the chemistry by plasma, and remains at low temperature in the plasma discharge (~200K measured by optical emission spectroscopy). Different N2-CH4-based gas mixtures can be injected in the plasma, with or without the addition of trace elements present on Titan. Both the gas phase and solid phase products resulting from the plasma-induced chemistry can be monitored and analyzed using a combination of complementary in situ and ex situ diagnostics: Cavity Ring Down Spectroscopy and Time-Of-Flight Mass Spectrometry (TOF-MS) for the gas phase; Direct Analysis in Real Time Mass Spectrometry (DART-MS), Gas Chromatography-Mass Spectrometry (GC-MS), Scanning Electron Microscopy (SEM), Raman spectroscopy, Nuclear Magnetic Resonance (NMR) and Infrared (IR) spectroscopy for the solid phase. Previous TOF-MS mass spectrometry analyses of the gas phase have demonstrated that the COSmIC/THS experiment can be used to study the first and intermediate steps as well as specific chemical pathways of Titan's atmospheric chemistry. The more complex chemistry, observed in the gas phase when adding trace elements to the initial N2-CH4 mixture, has been confirmed by an extensive study of the

  4. Cross-Institute Evaluations of Inhibitor-Resistant PCR Reagents for Direct Testing of Aerosol and Blood Samples Containing Biological Warfare Agent DNA

    PubMed Central

    Minogue, Timothy D.; Rachwal, Phillip A.; Trombley Hall, Adrienne; Koehler, Jeffery W.

    2014-01-01

    Rapid pathogen detection is crucial for the timely introduction of therapeutics. Two groups (one in the United Kingdom and one in the United States) independently evaluated inhibitor-resistant PCR reagents for the direct testing of substrates. In the United Kingdom, a multiplexed Bacillus anthracis (target) and Bacillus subtilis (internal-control) PCR was used to evaluate 4 reagents against 5 PCR inhibitors and down-selected the TaqMan Fast Virus 1-Step master mix (Life Technologies Inc.). In the United States, four real-time PCR assays (targeting B. anthracis, Brucella melitensis, Venezuelan equine encephalitis virus [VEEV], and Orthopoxvirus spp.) were used to evaluate 5 reagents (plus the Fast Virus master mix) against buffer, blood, and soil samples and down-selected the KAPA Blood Direct master mix (KAPA Biosystems Inc.) with added Platinum Taq (Life Technologies). The down-selected reagents underwent further testing. In the United Kingdom experiments, both reagents were tested against seven contrived aerosol collector samples containing B. anthracis Ames DNA and B. subtilis spores from a commercial formulation (BioBall). In PCR assays with reaction mixtures containing 40% crude sample, an airfield-collected sample induced inhibition of the B. subtilis PCR with the KAPA reagent and complete failure of both PCRs with the Fast Virus reagent. However, both reagents allowed successful PCR for all other samples—which inhibited PCRs with a non-inhibitor-resistant reagent. In the United States, a cross-assay limit-of-detection (LoD) study in blood was conducted. The KAPA Blood Direct reagent allowed the detection of agent DNA (by four PCRs) at higher concentrations of blood in the reaction mixture (2.5%) than the Fast Virus reagent (0.5%), although LoDs differed between assays and reagent combinations. Across both groups, the KAPA Blood Direct reagent was determined to be the optimal reagent for inhibition relief in PCR. PMID:24334660

  5. CONTAIN code analyses of direct containment heating (DCH) experiments: Model assessment and phenomenological interpretation

    SciTech Connect

    Williams, D.C.; Griffith, R.O.; Tadios, E.L.; Washington, K.E.

    1995-05-12

    Models for direct containment heating (DCH) in the CONTAIN code for severe accident analysis have been reviewed and a standard input prescription for their use has been defined. The code has been exercised against a large subset of the available DCH data base. Generally good agreement with the experimental results for containment pressurization ({Delta}P) and hydrogen generation has been obtained. Extensive sensitivity studies have been performed which permit assessment of many of the strengths and weaknesses of specific model features. These include models for debris transport and trapping, DCH heat transfer and chemistry, atmosphere-structure heat transfer, interactions between nonairborne debris and blowdown steam, potential effects of debris-water interactions, and hydrogen combustion under DCH conditions. Containment compartmentalization is an important DCH mitigator in the calculations, in agreement with experimental results. The CONTAIN model includes partially parametric treatments for some processes that are not well understood. The importance of the associated uncertainties depends upon the details of the DCH scenario being analyzed. Recommended sensitivity studies are summarized that allow the user to obtain a reasonable estimate of the uncertainties in the calculated results.

  6. Laboratory experiments on cluster/aerosol formation by colliding ablation plumes

    NASA Astrophysics Data System (ADS)

    Hirooka, Y.; Tanaka, K. A.; Sato, H.; Ishihara, K.; Sunahara, A.

    2010-08-01

    First-of-a-kind experiments on cluster/aerosol formation by colliding ablation plumes have been conducted, radiating Al, Cu and C with 3ω-YAG laser at power densities between 2~30 J/cm2/pulse. Visible spectroscopy indicates that the excitation light intensities of Cu and Al plumes are not necessarily be doubled in collision, but can rather be weakened due to atomic and molecular reactions. For colliding C plumes, Swan band radiation has been observed, indicative of C2 and/or C2+ formation, and ion mass spectrometry has identified Cn+-clusters, including C+, C2+, C3+, C4+ and C5+. From ICCD camera observations, C plumes generated at power densities above ~15 J/cm2/pulse tend to split into two components with respective velocities, only the slow component of which appears to be interactive to form clusters. Nano structures like CNT have been identified in deposits from colliding C plumes.

  7. Stratospheric ozone variations in the equatorial region as seen in Stratiospheric Aerosol and Gas Experiment data

    NASA Technical Reports Server (NTRS)

    Shiotani, Masato; Hasebe, Fumio

    1994-01-01

    An analysis is made of equatorial ozone variations for 5 years, 1984-1989, using the ozone profile data derived from the Stratospheric Aerosol and Gas Experiment II (SAGE II) instrument. Attention is focused on the annual cycle and also on interannual variability, particularly the quasi-biennial oscillation (QBO) and El Nino-Southern Oscillation (ENSO) variations in the lower stratosphere, where the largest contribution to total column ozone takes place. The annual variation in zonal mean total ozone around the equator is composed of symmetric and asymmetric modes with respect to the equator, with maximum contributions being around 19 km for the symmetric mode and around 25 km for the asymmetric mode. The persistent zonal wavenumber 1 structure observed by the total ozone mapping spectrometer over the equator is almost missing in the SAGE-derived column amounts integrated in the stratosphere, suggesting a significant contribution from tropospheric ozone. Interannual variations in the equatorial ozone are dominated by the QBO above 20 km and the ENSO-related variation below 20 km. The ozone QBO is characterized by zonally uniform phase changes in association with the zonal wind QBO in the equatorial lower stratosphere. The ENSO-related ozone variation consists of both the east-west vacillation and the zonally uniform phase variation. During the El Nino event, the east-west contrast with positive (negative) deviations in the eastern (western) hemisphere is conspicuous, while the decreasing tendency of the zonal mean values is maximum at the same time.

  8. From Clusters to Atmospheric Aerosol Particles: Nucleation in the CLOUD Experiment at CERN

    NASA Astrophysics Data System (ADS)

    Baltensperger, Urs

    2015-03-01

    Globally, a significant source of cloud condensation nuclei for cloud formation is thought to originate from new particle formation (aerosol nucleation). Despite extensive research, many questions remain about the dominant nucleation mechanisms. Specifically, a quantitative understanding of the dependence of the nucleation rate on the concentration of the nucleating substances such as gaseous sulfuric acid, ammonia, water vapor and others has not been reached. This is of relevance for climate as the atmospheric concentrations of sulfuric acid, ammonia and other nucleating agents are strongly influenced by anthropogenic emissions. By providing extremely well controlled and essentially contaminant free conditions in the CLOUD chamber, we were able to show that indeed sulfuric acid is an important component for such new particle formation, however, for the typical temperatures encountered in the planetary boundary layer the concentrations of sulfuric acid are not high enough to explain the atmospheric observations. Moreover, the effect of ammonia, amines and oxidized organic molecules on the nucleation rate of sulfuric acid has been investigated in CLOUD so far. Recent developments in instrument technology such as the Atmospheric Pressure interface-Time Of Flight (APi-TOF) mass spectrometer have allowed us to investigate the chemical composition of charged as well as neutral clusters during such nucleation experiments. The CLOUD (Cosmics Leaving OUtdoor Droplets) collaboration consists of 20 institutions from Europe and the United States and is funded by national funding institutions as well as the EU training network CLOUD-TRAIN (http://www.cloud-train.eu/).

  9. Stratospheric ozone variations in the equatorial region as seen in Stratiospheric Aerosol and Gas Experiment data

    SciTech Connect

    Shiotani, M.; Hasebe, F. |

    1994-07-01

    An analysis is made of equatorial ozone variations for 5 years, 1984-1989, using the ozone profile data derived from the Stratospheric Aerosol and Gas Experiment II (SAGE II) instrument. Attention is focused on the annual cycle and also on interannual variability, particularly the quasi-biennial oscillation (QBO) and El Nino-Southern Oscillation (ENSO) variations in the lower stratosphere, where the largest contribution to total column ozone takes place. The annual variation in zonal mean total ozone around the equator is composed of symmetric and asymmetric modes with respect to the equator, with maximum contributions being around 19 km for the symmetric mode and around 25 km for the asymmetric mode. The persistent zonal wavenumber 1 structure observed by the total ozone mapping spectrometer over the equator is almost missing in the SAGE-derived column amounts integrated in the stratosphere, suggesting a significant contribution from tropospheric ozone. Interannual variations in the equatorial ozone are dominated by the QBO above 20 km and the ENSO-related variation below 20 km. The ozone QBO is characterized by zonally uniform phase changes in association with the zonal wind QBO in the equatorial lower stratosphere. The ENSO-related ozone variation consists of both the east-west vacillation and the zonally uniform phase variation. During the El Nino event, the east-west contrast with positive (negative) deviations in the eastern (western) hemisphere is conspicuous, while the decreasing tendency of the zonal mean values is maximum at the same time.

  10. Dimers and organosulfates derived from biogenic oxidation products in aerosols during the Biosphere Effects on Aerosols and Photochemistry Experiment (BEARPEX) in California 2007 and 2009 (Invited)

    NASA Astrophysics Data System (ADS)

    Glasius, M.; Worton, D. R.; Kristensen, K.; Nguyen, Q.; Surratt, J.; Enggrob, K. L.; Bouvier-Brown, N. C.; Farmer, D.; Docherty, K. S.; Platt, S.; Bilde, M.; Nøjgaard, J. K.; Seinfeld, J.; Jimenez, J. L.; Goldstein, A.

    2010-12-01

    Oxidation products of biogenic volatile organic compounds, such as monoterpenes and isoprene, contribute to biogenic secondary organic aerosol (BSOA). The organosulfate derivatives of these compounds are formed through heterogeneous reactions involving sulphur compounds, with a considerable contribution from anthropogenic sources. Organosulfate derivatives of biogenic oxidation products thus belong to a new group of anthropogenic enhanced biogenic SOA (ABSOA). The Biosphere Effects on Aerosols and Photochemistry Experiment (BEARPEX) during summers of 2007 and 2009 provided an excellent platform at Blodgett Forest, California (a ponderosa pine plantation) for studying ABSOA. Typically, polluted air masses were transported upslope from the California Central Valley during day, while night conditions were influenced by downslope transport of air masses, low local atmospheric mixing and formation of a shallow boundary layer. We collected particle samples (PM2.5) as one nighttime and two daytime samples per day. After extraction of filters in polar organic solvents (i.e. acetonitrile or methanol), organic aerosol constituents were analyzed by HPLC coupled through an electrospray inlet to a quadrupole time-of-flight mass spectrometer (qTOF-MS). Organosulfates and nitrooxy organosulfates derived from oxidation products of α-pinene, β-pinene, limonene and isoprene were identified based on their molecular mass and MS fragmentation patterns. Measurements by High Resolution Time of Flight Aerosol Mass Spectrometry (HR-ToF-AMS) show high mass loadings of nitrate in the night and morning samples with highest levels of the nitrooxy organosulfates with MW 295 and MW 297. This may indicate that elevated levels of nitrate and nitrooxy organosulfates are formed in the same polluted air mass, probably through nitrate radical reactions. Terpenylic acid, diterpenylic acid acetate, and methylbutane tricarboxylic acid were found at concentrations comparable to pinic acid. A dimer of

  11. Heterogeneous ice nucleation on atmospheric aerosols: a review of results from laboratory experiments

    NASA Astrophysics Data System (ADS)

    Hoose, C.; Möhler, O.

    2012-10-01

    A small subset of the atmospheric aerosol population has the ability to induce ice formation at conditions under which ice would not form without them (heterogeneous ice nucleation). While no closed theoretical description of this process and the requirements for good ice nuclei is available, numerous studies have attempted to quantify the ice nucleation ability of different particles empirically in laboratory experiments. In this article, an overview of these results is provided. Ice nucleation "onset" conditions for various mineral dust, soot, biological, organic and ammonium sulfate particles are summarized. Typical temperature-supersaturation regions can be identified for the "onset" of ice nucleation of these different particle types, but the various particle sizes and activated fractions reported in different studies have to be taken into account when comparing results obtained with different methodologies. When intercomparing only data obtained under the same conditions, it is found that dust mineralogy is not a consistent predictor of higher or lower ice nucleation ability. However, the broad majority of studies agrees on a reduction of deposition nucleation by various coatings on mineral dust. The ice nucleation active surface site (INAS) density is discussed as a simple and empirical normalized measure for ice nucleation activity. For most immersion and condensation freezing measurements on mineral dust, estimates of the temperature-dependent INAS density agree within about two orders of magnitude. For deposition nucleation on dust, the spread is significantly larger, but a general trend of increasing INAS densities with increasing supersaturation is found. For soot, the presently available results are divergent. Estimated average INAS densities are high for ice-nucleation active bacteria at high subzero temperatures. At the same time, it is shown that INAS densities of some other biological aerosols, like certain pollen grains, fungal spores and diatoms

  12. Heterogeneous ice nucleation on atmospheric aerosols: a review of results from laboratory experiments

    NASA Astrophysics Data System (ADS)

    Hoose, C.; Möhler, O.

    2012-05-01

    A small subset of the atmospheric aerosol population has the ability to induce ice formation at conditions under which ice would not form without them (heterogeneous ice nucleation). While no closed theoretical description of this process and the requirements for good ice nuclei is available, numerous studies have attempted to quantify the ice nucleation ability of different particles empirically in laboratory experiments. In this article, an overview of these results is provided. Ice nucleation onset conditions for various mineral dust, soot, biological, organic and ammonium sulphate particles are summarized. Typical temperature-supersaturation regions can be identified for the onset of ice nucleation of these different particle types, but the various particle sizes and activated fractions reported in different studies have to be taken into account when comparing results obtained with different methodologies. When intercomparing only data obtained under the same conditions, it is found that dust mineralogy is not a consistent predictor of higher or lower ice nucleation ability. However, the broad majority of studies agrees on a reduction of deposition nucleation by various coatings on mineral dust. The ice nucleation active surface site (INAS) density is discussed as a normalized measure for ice nucleation activity. For most immersion and condensation freezing measurements on mineral dust, estimates of the temperature-dependent INAS density agree within about two orders of magnitude. For deposition nucleation on dust, the spread is significantly larger, but a general trend of increasing INAS densities with increasing supersaturation is found. For soot, the presently available results are divergent. Estimated average INAS densities are high for ice-nucleation active bacteria at high subzero temperatures. At the same time, it is shown that some other biological aerosols, like certain pollen grains and fungal spores, are not intrinsically better ice nuclei than dust

  13. Capillary Flow in Containers of Polygonal Section: Theory and Experiment

    NASA Technical Reports Server (NTRS)

    Weislogel, Mark M.; Rame, Enrique (Technical Monitor)

    2001-01-01

    An improved understanding of the large-length-scale capillary flows arising in a low-gravity environment is critical to that engineering community concerned with the design and analysis of spacecraft fluids management systems. Because a significant portion of liquid behavior in spacecraft is capillary dominated it is natural to consider designs that best exploit the spontaneous character of such flows. In the present work, a recently verified asymptotic analysis is extended to approximate spontaneous capillary flows in a large class of cylindrical containers of irregular polygonal section experiencing a step reduction in gravitational acceleration. Drop tower tests are conducted using partially-filled irregular triangular containers for comparison with the theoretical predictions. The degree to which the experimental data agree with the theory is a testament to the robustness of the basic analytical assumption of predominantly parallel flow. As a result, the closed form analytical expressions presented serve as simple, accurate tools for predicting bulk flow characteristics essential to practical low-g system design and analysis. Equations for predicting corner wetting rates, total container flow rates, and transient surfaces shapes are provided that are relevant also to terrestrial applications such as capillary flow in porous media.

  14. Overview of Asian Biomass Burning and Dust Aerosols Measured during the Dongsha Experiment in the Spring of 2010

    NASA Astrophysics Data System (ADS)

    Lin, N.; Tsay, S.; Wang, S.; Sheu, G.; Chi, K.; Lee, C.; Wang, J.

    2010-12-01

    The international campaign of Dongsha Experiment was conducted in the northern SE Asian region during March-May 2010. It is a pre-study of the Seven South East Asian Studies (7SEAS) which seeks to perform interdisciplinary research in the field of aerosol-meteorology and climate interaction in the Southeast Asian region, particularly for the impact of biomass burning on cloud, atmospheric radiation, hydrological cycle, and regional climate. Participating countries include Indonesia, Malaysia, Philippines, Singapore, Thailand, Taiwan, Vietnam, and USA (NASA, NRL, and NOAA). The main goals of Dongsha Experiment are (1) to develop the Dongsha Island (about 2 km2, 20°42'52" N, 116°43'51" E) in the South China Sea as an atmospheric observing platform of atmospheric chemistry, radiation and meteorological parameters, and (2) to characterize the chemical and physical properties of biomass burning aerosols in the northern SE Asian region. A monitoring network for ground-based measurements includes the Lulin Atmospheric Background Station (2,862 m MSL) in central Taiwan, Hen-Chun (coastal) in the very southern tip of Taiwan, Dongsha Island in South China Sea, Da Nang (near coastal region) in central Vietnam, and Chiang Mai (about 1,400 m, MSL) in northern Thailand. Besides, the Mobile Air Quality Station of Taiwan EPA and NASA/COMMIT were shipped to Dongsha Island for continuous measurements of CO, SO2, NOx, O3, and PM10, and aerosol optical and vertical profiles. Two Intensive Observation Periods (IOPs) for aerosol chemistry were conducted during 14-30 March and 10-20 April 2010, respectively. Ten aerosol samplers were deployed for each station for characterizing the compositions of PM2.5/PM10 (some for TSP) including water-soluble ions, metal elements, BC/OC, Hg and dioxins. Sampling tubes of VOCs were also deployed. Concurrent measurements with IOP-1, Taiwanese R/V also made a mission to South China Sea during 14-19 March. Enhanced sounding at Dongsha Island was

  15. Particle Morphology and Size Results from the Smoke Aerosol Measurement Experiment-2

    NASA Technical Reports Server (NTRS)

    Urban, David L.; Ruff, Gary A.; Greenberg, Paul S.; Fischer, David; Meyer, Marit; Mulholland, George; Yuan, Zeng-Guang; Bryg, Victoria; Cleary, Thomas; Yang, Jiann

    2012-01-01

    Results are presented from the Reflight of the Smoke Aerosol Measurement Experiment (SAME-2) which was conducted during Expedition 24 (July-September 2010). The reflight experiment built upon the results of the original flight during Expedition 15 by adding diagnostic measurements and expanding the test matrix. Five different materials representative of those found in spacecraft (Teflon, Kapton, cotton, silicone rubber and Pyrell) were heated to temperatures below the ignition point with conditions controlled to provide repeatable sample surface temperatures and air flow. The air flow past the sample during the heating period ranged from quiescent to 8 cm/s. The smoke was initially collected in an aging chamber to simulate the transport time from the smoke source to the detector. This effective transport time was varied by holding the smoke in the aging chamber for times ranging from 11 to 1800 s. Smoke particle samples were collected on Transmission Electron Microscope (TEM) grids for post-flight analysis. The TEM grids were analyzed to observe the particle morphology and size parameters. The diagnostics included a prototype two-moment smoke detector and three different measures of moments of the particle size distribution. These moment diagnostics were used to determine the particle number concentration (zeroth moment), the diameter concentration (first moment), and the mass concentration (third moment). These statistics were combined to determine the diameter of average mass and the count mean diameter and, by assuming a log-normal distribution, the geometric mean diameter and the geometric standard deviations can also be calculated. Overall the majority of the average smoke particle sizes were found to be in the 200 nm to 400 nm range with the quiescent cases producing some cases with substantially larger particles.

  16. LASE measurements of water vapor and aerosol profiles during the Plains Elevated Convection at Night (PECAN) field experiment

    NASA Astrophysics Data System (ADS)

    Nehrir, A. R.; Ferrare, R. A.; Kooi, S. A.; Butler, C. F.; Notari, A.; Hair, J. W.; Collins, J. E., Jr.; Ismail, S.

    2015-12-01

    The Lidar Atmospheric Sensing Experiment (LASE) system was deployed on the NASA DC-8 aircraft during the Plains Elevated Convection At Night (PECAN) field experiment, which was conducted during June-July 2015 over the central and southern plains. LASE is an active remote sensor that employs the differential absorption lidar (DIAL) technique to measure range resolved profiles of water vapor and aerosols above and below the aircraft. The DC-8 conducted nine local science flights from June 30- July 14 where LASE sampled water vapor and aerosol fields in support of the PECAN primary science objectives relating to better understanding nocturnal Mesoscale Convective Systems (MCSs), Convective Initiation (CI), the Low Level Jet (LLJ), bores, and to compare different airborne and ground based measurements. LASE observed large spatial and temporal variability in water vapor and aerosol distributions in advance of nocturnal MCSs, across bores resulting from MCS outflow boundaries, and across the LLJ associated with the development of MCSs and CI. An overview of the LASE data collected during the PECAN field experiment will be presented where emphasis will be placed on variability of water vapor profiles in the vicinity of severe storms and intense convection in the central and southern plains. Preliminary comparisons show good agreement between coincident LASE and radiosonde water vapor profiles. In addition, an advanced water vapor DIAL system being developed at NASA Langley will be discussed.

  17. The Joint Aerosol-Monsoon Experiment (JAMEX): A Core Element for the Asian Monsoon Year (2008-2009)

    NASA Technical Reports Server (NTRS)

    Lau, WIlliam K. M.

    2007-01-01

    The objective of the Joint Aerosol-Monsoon Experiment (JAMEX) is to unravel the physical mechanisms and multi-scale interactions associated with aerosol-monsoon water cycle in the Asian Indo-Paczj?c region towards improved prediction of rainfall in land regions of the Asian monsoon. JAMEX will be planned as a five-year (2007-201 1) multi-national aerosol-monsoon research project, aimed at promoting collaboration, partnership and alignment of ongoing and planned national and international programs. Two coordinated special observing periods (SOP), covering the pre-monsoon (April-May) and the monsoon (June-August) periods is tentatively targeted for 2008 and 2009. The major work on validation and reference site coordination will take place in 2007 through the spring of 2008. A major science workshop is planned after SOP-I1 in 2010. Modeling and satellite data utilization studies will continue throughout the entire period to help in design of the observation arrays and measurement platforms for SOPS. The tentative time schedule, including milestones and research activities is shown in Fig. 1. One of the unique aspects of JAMEX is that it stems from grass-root scientific and societal imperatives, and it bridges a gap in existing national and international research programs. Currently we have identified 10 major national and international projects/programs separately for aerosols and monsoon research planned in the next five years in China, India, Japan, Italy, and the US, that could be potential contributors or partners with JAMEX. These include the Asian-Indo- Pacific Ocean (AIPO) Project and Aerosol Research Project from China, Monsoon Asian Hydro- Atmospheric Science Research and predication Initiative (MAHASRI) from Japan, Continental Tropical Convergence Zone (CTCZ) and Severe Thunderstorm: Observations and Regional Modeling (STORM) from India, Share-Asia from Italy, Atmospheric Brown Cloud (ABC), Pacific Aerosol-Cloud-Dust Experiment (PACDEX), East Asia Study of

  18. The Joint Aerosol-Monsoon Experiment (JAMEX): A Core Element for the Asian Monsoon Year (2008-2009)

    NASA Technical Reports Server (NTRS)

    Lau, William K.M.

    2007-01-01

    The objective of the Joint Aerosol-Monsoon Experiment (JAMEX) is to unravel the physical mechanisms and multi-scale interactions associated with aerosol-monsoon water cycle in the Asian Indo-Pacific region towards improved prediction of rainfall in land regions of the Asian monsoon. JAMEX will be planned as a five-year (2007-201 1) multi-national aerosol-monsoon research project, aimed at promoting collaboration, partnership and alignment of ongoing and planned national and international programs. Two coordinated special observing periods (SOP), covering the pre-monsoon (April-May) and the monsoon (June-August) periods is tentatively targeted for 2008 and 2009. The major work on validation and reference site coordination will take place in 2007 through the spring of 2008. A major science workshop is planned after SOP-I1 in 2010. Modeling and satellite data utilization studies will continue throughout the entire period to help in design of the observation arrays and measurement platforms for SOPS. The tentative time schedule, including milestones and research activities is shown in Fig. 1. One of the unique aspects of JAMEX is that it stems from grass-root scientific and societal imperatives, and it bridges a gap in existing national and international research programs. Currently we have identified 10 major national and international projects/programs separately for aerosols and monsoon research planned in the next five years in China, India, Japan, Italy, and the US, that could be potential contributors or partners with JAMEX. These include the Asian-Indo- Pacific Ocean (AIPO) Project and Aerosol Research Project from China, Monsoon Asian Hydro- Atmospheric Science Research and predication Initiative (MAHASRI) from Japan, Continental Tropical Convergence Zone (CTCZ) and Severe Thunderstorm: Observations and Regional Modeling (STORM) from India, Share-Asia from Italy, Atmospheric Brown Cloud (ABC), Pacific Aerosol-Cloud-Dust Experiment (PACDEX), East Asia Study of

  19. Interpretation of FRESCO cloud retrievals in case of absorbing aerosol events

    NASA Astrophysics Data System (ADS)

    Wang, P.; Tuinder, O. N. E.; Tilstra, L. G.; de Graaf, M.; Stammes, P.

    2012-10-01

    Cloud and aerosol information is needed in trace gas retrievals from satellite measurements. The Fast REtrieval Scheme for Clouds from the Oxygen A band (FRESCO) cloud algorithm employs reflectance spectra of the O2 A band around 760 nm to derive cloud pressure and effective cloud fraction. In general, clouds contribute more to the O2 A band reflectance than aerosols. Therefore, the FRESCO algorithm does not correct for aerosol effects in the retrievals and attributes the retrieved cloud information entirely to the presence of clouds, and not to aerosols. For events with high aerosol loading, aerosols may have a dominant effect, especially for almost cloud free scenes. We have analysed FRESCO cloud data and Absorbing Aerosol Index (AAI) data from the Global Ozone Monitoring Experiment (GOME-2) instrument on the Metop-A satellite for events with typical absorbing aerosol types, such as volcanic ash, desert dust and smoke. We find that the FRESCO effective cloud fractions are correlated with the AAI data for these absorbing aerosol events and that the FRESCO cloud pressure contains information on aerosol layer pressure. For cloud free scenes, the derived FRESCO cloud pressure is close to the aerosol layer pressure, especially for optically thick aerosol layers. For cloudy scenes, if the strongly absorbing aerosols are located above the clouds, then the retrieved FRESCO cloud pressure may represent the height of the aerosol layer rather than the height of the clouds. Combining FRESCO and AAI data, an estimate for the aerosol layer pressure can be given.

  20. SUBMERGED GRAVEL SCRUBBER DEMONSTRATION AS A PASSIVE AIR CLEANER FOR CONTAINMENT VENTING AND PURGING WITH SODIUM AEROSOLS -- CSTF TESTS AC7 - AC10

    SciTech Connect

    HILLIARD, R K.; MCCORMACK, J D.; POSTMA, A K.

    1981-11-01

    Four large-scale air cleaning tests (AC7 - AC10) were performed in the Containment Systems Test Facility (CS'lF) to demonstrate the performance of a Submerged Gravel Scrubber for cleaning the effluent gas from a vented and purged breeder reactor containment vessel. The test article, comprised of a Submerged Gravel Scrubber (SGS) followed by a high efficiency fiber demister, had a design gas flow rate of 0.47 m{sup 3}/s (1000 ft{sup 3}/min) at a pressure drop of 9.0 kPa (36 in. H{sub 2}O). The test aerosol was sodium oxide, sodium hydroxide, or sodium carbonate generated in the 850-m{sup 3} CSTF vessel by continuously spraying sodium into the air-filled vessel while adding steam or carbon dioxide. Approximately 4500 kg (10,000 lb) of sodium was sprayed over a total period of 100 h during the tests. The SGS/Demister system was shown to be highly efficient (removing ~99.98% of the entering sodium aerosol mass), had a high mass loading capacity, and operated in a passive manner, with no electrical requirement. Models for predicting aerosol capture, gas cooling, and pressure drop are developed and compared with experimental results.

  1. The Stratospheric Aerosol and Gas Experiment III/International Space Station Mission: Science Objectives and Mission Status

    NASA Astrophysics Data System (ADS)

    Eckman, R.; Zawodny, J. M.; Cisewski, M. S.; Flittner, D. E.; McCormick, M. P.; Gasbarre, J. F.; Damadeo, R. P.; Hill, C. A.

    2015-12-01

    The Stratospheric Aerosol and Gas Experiment III/International Space Station (SAGE III/ISS) is a strategic climate continuity mission which was included in NASA's 2010 plan, "Responding to the Challenge of Climate and Environmental Change: NASA's Plan for a Climate-Centric Architecture for Earth Observations and Applications from Space." SAGE III/ISS continues the long-term, global measurements of trace gases and aerosols begun in 1979 by SAGE I and continued by SAGE II and SAGE III on Meteor 3M. Using a well characterized occultation technique, the SAGE III instrument's spectrometer will measure vertical profiles of ozone, aerosols, water vapor, nitrogen dioxide, and other trace gases relevant to ozone chemistry. The mission will launch in 2016 aboard a Falcon 9 spacecraft.The primary objective of SAGE III/ISS is to monitor the vertical distribution of aerosols, ozone, and other trace gases in the Earth's stratosphere and troposphere to enhance our understanding of ozone recovery and climate change processes in the stratosphere and upper troposphere. SAGE III/ISS will provide data necessary to assess the state of the recovery in the distribution of ozone, extend the SAGE III aerosol measurement record that is needed by both climate models and ozone models, and gain further insight into key processes contributing to ozone and aerosol variability. The multi-decadal SAGE ozone and aerosol data sets have undergone intense community scrutiny for accuracy and stability. SAGE ozone data have been used to monitor the effectiveness of the Montreal Protocol.The ISS inclined orbit of 51.6 degrees is ideal for SAGE III measurements because the orbit permits solar occultation measurement coverage to approximately +/- 70 degrees of latitude. SAGE III/ISS will make measurements using the solar occultation measurement technique, lunar occultation measurement technique, and the limb scattering measurement technique. In this presentation, we describe the SAGE III/ISS mission, its

  2. Dust Aerosol Optical Properties Retrieval and Radiative Forcing over Northwestern China during 2008 China-US Joint Field Experiment

    NASA Astrophysics Data System (ADS)

    Ge, J.; Su, J.; Ackerman, T. P.; Fu, Q.; Huang, J.; Shi, J.

    2009-12-01

    The Atmosphere Radiation Measurements (ARM) Program’s Ancillary Facility (AAF/SMART-COMMIT) was deployed to Zhangye (39.082° N, 100.276° E), which is located in a semi-desert area of Northwest China, during the period of late April to mid June in 2008. We selected 11 cases to retrieve dust aerosol optical depth (AOD), Angstrom exponent, size distribution, single-scattering albedo (SSA) and asymmetry parameter (ASY) from Multi-filter Rotating Shadowband Radiometer (MFRSR) measurements. These cases are dominated by large particles with Angstrom exponent values ranging from 0.34 to 0.93. The values of AOD at 0.67 µm range from 0.074 to 0.249. The mean SSA value increases with wavelength from 0.76±0.02 at 0.415 µm to 0.86±0.01 at 0.867 µm, while the mean ASY value decreases from 0.74±0.04 to 0.70±0.02. Before estimating dust aerosol direct radiative forcing, a radiative closure experiment was performed to verify that the retrieved aerosol optical properties and other input parameters to the radiative transfer model appropriately represent atmospheric conditions. The daytime-averaged differences between model simulations and ground observations are -8.5, -2.9, and -2.1 Wm-2 for the total, diffuse, and direct normal fluxes, respectively. The mean difference in the instantaneous reflected solar fluxes at the top of atmosphere (TOA) between the model and CERES observations is 8.0 Wm-2. The solar aerosol direct radiative forcing (ARF), averaged over a 24-hour period, at the surface is-22.4±8.9 Wm-2, while the TOA ARF is small and has an average value of only 0.52±1.69 Wm-2. The daily-average surface aerosol radiative forcing efficiency (ARFE) at 0.5 µm is -95.1±10.3 Wm-2τ-1. Our results illustrate that the primary role of dust aerosol is to alter the distribution of solar radiation within the climate system, rather than reflecting solar energy to space. We assess the satellite aerosol optical depth products from MISR and MODIS observations by comparing them

  3. Intercomparison of stratospheric water vapor observed by satellite experiments - Stratospheric Aerosol and Gas Experiment II versus Limb Infrared Monitor of the Stratosphere and Atmospheric Trace Molecule Spectroscopy

    NASA Technical Reports Server (NTRS)

    Chiou, E. W.; Mccormick, M. P.; Mcmaster, L. R.; Chu, W. P.; Larsen, J. C.; Rind, D.; Oltmans, S.

    1993-01-01

    A comparison is made of the stratospheric water vapor measurements made by the satellite sensors of the Stratospheric Aerosol and Gas Experiment II (SAGE II), the Nimbus-7 LIMS, and the Spacelab 3 Atmospheric Trace Molecule Spectroscopy (ATMOS) experiment. It was found that, despite differences in the measurement techniques, sampling bias, and observational periods, the three experiments have disclosed a generally consistent pattern of stratospheric water vapor distribution. The only significant difference occurs at high southern altitudes in May below 18 km, where LIMS measurements were 2-3 ppmv greater than those of SAGE II and ATMOS.

  4. An Overview of Regional Experiments on Biomass Burning Aerosols and Related Pollutants in Southeast Asia: From BASE-ASIA and the Dongsha Experiment to 7-SEAS

    NASA Technical Reports Server (NTRS)

    Lin, Neng-Huei; Tsay, Si-Chee; Maring, Hal B.; Yen, Ming-Cheng; Sheu, Guey-Rong; Wang, Sheng-Hsiang; Chi, Kai Hsien; Chuang, Ming-Tung; Ou-Yang, Chang-Feng; Fu, Joshua S.; Reid, Jeffrey S.; Lee, Chung-Te; Wang, Lin-Chi; Wang, Jia-Lin; Hsu, Christina N.; Sayer, Andrew M.; Holben, Brent N.; Chu, Yu-Chi; Nguyen, Xuan Anh; Sopajaree, Khajornsak; Chen, Shui-Jen; Cheng, Man-Ting; Tsuang, Ben-Jei; Tsai, Chuen-Jinn; Peng, Chi-Ming; Schnell, Russell C.; Conway, Tom; Chang, Chang-Tang; Lin, Kuen-Song; Tsai, Ying I.; Lee, Wen-Jhy; Chang, Shuenn-Chin; Liu, Jyh-Jian; Chang, Wei-Li; Huang, Shih-Jen; Lin, Tang-Huang; Liu, Gin-Rong

    2013-01-01

    By modulating the Earth-atmosphere energy, hydrological and biogeochemical cycles, and affecting regional-to-global weather and climate, biomass burning is recognized as one of the major factors affecting the global carbon cycle. However, few comprehensive and wide-ranging experiments have been conducted to characterize biomass-burning pollutants in Southeast Asia (SEA) or assess their regional impact on meteorology, the hydrological cycle, the radiative budget, or climate change. Recently, BASEASIA (Biomass-burning Aerosols in South-East Asia: Smoke Impact Assessment) and the 7-SEAS (7- South-East Asian Studies) Dongsha Experiment were conducted during the spring seasons of 2006 and 2010 in northern SEA, respectively, to characterize the chemical, physical, and radiative properties of biomass-burning emissions near the source regions, and assess their effects. This paper provides an overview of results from these two campaigns and related studies collected in this special issue, entitled Observation, modeling and impact studies of biomass burning and pollution in the SE Asian Environment. This volume includes 28 papers, which provide a synopsis of the experiments, regional weatherclimate, chemical characterization of biomass-burning aerosols and related pollutants in source and sink regions, the spatial distribution of air toxics (atmospheric mercury and dioxins) in source and remote areas, a characterization of aerosol physical, optical, and radiative properties, as well as modeling and impact studies. These studies, taken together, provide the first relatively complete dataset of aerosol chemistry and physical observations conducted in the sourcesink region in the northern SEA, with particular emphasis on the marine boundary layer and lower free troposphere (LFT). The data, analysis and modeling included in these papers advance our present knowledge of source characterization of biomass-burning pollutants near the source regions as well as the physical and

  5. Organic Composition of Size-Segregated Aerosols Sampled During the 2002 Bay Regional Atmospheric Chemistry Experiment (BRACE), Florida, USA

    NASA Astrophysics Data System (ADS)

    Tremblay, R. T.; Zika, R. G.

    2003-04-01

    Aerosol samples were collected for the analysis of organic source markers using non-rotating Micro Orifice Uniform Deposit Impactors (MOUDI) as part of the Bay Regional Atmospheric Chemistry Experiment (BRACE) in Tampa, FL, USA. Daily samples were collected 12 m above ground at a flow rate of 30 lpm throughout the month of May 2002. Aluminum foil discs were used to sample aerosol size fractions with aerodynamic cut diameter of 18, 10, 5.6, 3.2, 1.8, 1.0, 0.56, 0.32, 0.17 and 0.093 um. Samples were solvent extracted using a mixture of dichloromethane/acetone/hexane, concentrated and then analyzed using gas chromatography-mass spectrometry (GC/MS). Low detection limits were achieved using a HP Programmable Temperature Vaporizing inlet (PTV) and large volume injections (80ul). Excellent chromatographic resolution was obtained using a 60 m long RTX-5MS, 0.25 mm I.D. column. A quantification method was built for over 90 organic compounds chosen as source markers including straight/iso/anteiso alkanes and polycyclic aromatic hydrocarbons (PAH). The investigation of potential aerosol sources for different particle sizes using known organic markers and source profiles will be presented. Size distributions of carbon preference indices (CPI), percent wax n-alkanes (%WNA) and concentration of selected compounds will be discussed. Also, results will be compared with samples acquired in different environments including the 1999 Atlanta SuperSite Experiment, GA, USA.

  6. Successful experimental induction of acute malignant catarrhal fever in bison using aerosols of ovine nasal mucus containing ovine herpesvirus 2

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Malignant catarrhal fever is a common and fatal disease of American bison. Recently our group demonstrated that MCF can be induced experimentally in American bison by aerosol exposure to nasal secretions derived from sheep experiencing intensive shedding events. In the current study, we defined pr...

  7. Discrimination of water, ice and aerosols by light polarisation in the CLOUD experiment

    NASA Astrophysics Data System (ADS)

    Nichman, L.; Fuchs, C.; Järvinen, E.; Ignatius, K.; Höppel, N. F.; Dias, A.; Heinritzi, M.; Simon, M.; Tröstl, J.; Wagner, A. C.; Wagner, R.; Williamson, C.; Yan, C.; Bianchi, F.; Connolly, P. J.; Dorsey, J. R.; Duplissy, J.; Ehrhart, S.; Frege, C.; Gordon, H.; Hoyle, C. R.; Kristensen, T. B.; Steiner, G.; Donahue, N. M.; Flagan, R.; Gallagher, M. W.; Kirkby, J.; Möhler, O.; Saathoff, H.; Schnaiter, M.; Stratmann, F.; Tomé, A.

    2015-11-01

    Cloud microphysical processes involving the ice phase in tropospheric clouds are among the major uncertainties in cloud formation, weather and General Circulation Models (GCMs). The simultaneous detection of aerosol particles, liquid droplets, and ice crystals, especially in the small cloud-particle size range below 50 μm, remains challenging in mixed phase, often unstable ice-water phase environments. The Cloud Aerosol Spectrometer with Polarisation (CASPOL) is an airborne instrument that has the ability to detect such small cloud particles and measure their effects on the backscatter polarisation state. Here we operate the versatile Cosmics-Leaving-OUtdoor-Droplets (CLOUD) chamber facility at the European Organisation for Nuclear Research (CERN) to produce controlled mixed phase and other clouds by adiabatic expansions in an ultraclean environment, and use the CASPOL to discriminate between different aerosols, water and ice particles. In this paper, optical property measurements of mixed phase clouds and viscous Secondary Organic Aerosol (SOA) are presented. We report observations of significant liquid - viscous SOA particle polarisation transitions under dry conditions using CASPOL. Cluster analysis techniques were subsequently used to classify different types of particles according to their polarisation ratios during phase transition. A classification map is presented for water droplets, organic aerosol (e.g., SOA and oxalic acid), crystalline substances such as ammonium sulphate, and volcanic ash. Finally, we discuss the benefits and limitations of this classification approach for atmospherically relevant concentration and mixtures with respect to the CLOUD 8-9 campaigns and its potential contribution to Tropical Troposphere Layer (TTL) analysis.

  8. Optical properties of aerosols during APEX and ACE-Asia experiments

    NASA Astrophysics Data System (ADS)

    Sano, Itaru; Mukai, Sonoyo; Okada, Yasuhiko; Holben, Brent N.; Ohta, Sachio; Takamura, Tamio

    2003-12-01

    Sun/sky photometry and polarimetry of atmospheric light have been undertaken by multispectral photometers (CE-318-1 and -2, Cimel Electronique, France) and a polarimeter (PSR-1000, Opto Research, Japan) over Amami, Noto, and Shirahama, Japan, during APEX-E1, -E2, and ACE-Asia field campaigns. Radiometers provide us with the optical thickness of aerosols and Ångström exponent. Other aerosol characteristics, e.g., size distribution, refractive index, etc., are retrieved based on each inversion method corresponding each equipment. The former takes a standard AERONET processing, and the latter is according to our own procedure to analyze the polarimetry with PSR-1000. After several aerosol parameters are derived, the HYSPLIT4 backward trajectory analysis is adopted to search the origin of aerosols. It is shown from these ground measurements that aerosol optical thickness, Ångström exponent, and refractive index are classified into two typical categories as a background type detected in winter, and a soil dust type appeared in Asian dust events in spring. Further, it is found that the obtained size distribution of Asian dust indicates the dominance of large particles.

  9. Clinical experience with technetium-99m DTPA aerosol with perfusion scintigraphy in suspected pulmonary embolism

    SciTech Connect

    Selby, J.B.; Gardner, J.J.

    1987-01-01

    To evaluate the clinical value of radioaerosol imaging, 156 patients with suspected pulmonary embolism (PE) were studied. In 25 patients, a preperfusion xenon-133 (Xe-133) study was compared with a postperfusion study using Tc-99m DTPA aerosol. It was found that they were of equal value most of the time (56%), but that the aerosol study was more often helpful. Because of this, and the technical ease of using six standard views with radioaerosol, the series was completed using perfusion scintigraphy followed by radioaerosol images. In 19 patients the perfusion scintigraphy with Tc-99 macroaggregated albumin (Tc-99m MAA) was normal or nearly normal and no aerosol study was required. Tc-99m DTPA aerosol images were satisfactory when the count rate was at least twice and preferably three times that of the previous perfusion study. There were 17 studies (11%) classified as intermediate. There were 26 patients classified as high probability for PE, and angiographic or autopsy correlation was available in 14. All of the 14 proved to have PE. In the 113 patients classified as low probability, there were ten with angiographic or autopsy correlation. In the ten, there was one patient with a small pulmonary embolus found at autopsy. Clinical follow-up for over two months confirmed the absence of PE in the remainder of this group. Aerosol studies have proven technically easier to perform and a satisfactory substitute for xenon imaging in suspected PE.

  10. Ethical challenges of containing Ebola: the Nigerian experience.

    PubMed

    Maduka, Omosivie; Odia, Osaretin

    2015-11-01

    Responding effectively to an outbreak of disease often requires routine processes to be set aside in favour of unconventional approaches. Consequently, an emergency response situation usually generates ethical dilemmas. The emergence of the Ebola virus in the densely populated cities of Lagos and Port Harcourt in Nigeria brought bleak warnings of a rapidly expanding epidemic. However, these fears never materialised largely due to the swift reaction of emergency response and incident management organisations, and the WHO has now declared Nigeria free of Ebola. However, numerous ethical issues arose in relation to the response to the outbreak. This paper discusses some of these ethical challenges and the vital lessons learned. Ethical challenges relating to confidentiality, the dignity of persons, non-maleficence, stigma and the ethical obligations of health workers are examined. Interventions implemented to ensure that confidentiality and the dignity of persons improved and stigma was reduced, included community meetings, knowledge communication and the training of media personnel in the ethical reporting of Ebola issues. In addition, training in infection prevention and control helped to allay the fears of health workers. A potential disaster was also averted when the use of an experimental medicine was reconsidered. Other countries currently battling the epidemic can learn a lot from the Nigerian experience. PMID:26091816

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

    DOE Data Explorer

    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.

  12. Smog chamber experiments to investigate Henry's law constants of glyoxal using different seed aerosols

    NASA Astrophysics Data System (ADS)

    Jakob, Ronit

    2014-05-01

    Aerosols play an important role in the chemistry and physics of the atmosphere. Hence, they have a direct as well as an indirect impact on the earth's climate. Depending on their formation, one distinguishes between primary and secondary aerosols[1]. Important groups within the secondary aerosols are the secondary organic aerosols (SOAs). In order to improve predictions about these impacts on the earth's climate the existing models need to be optimized, because they still underestimate SOA formation[2]. Glyoxal, the smallest α-dicarbonyl, not only acts as a tracer for SOA formation but also as a direct contributor to SOA. Because glyoxal has such a high vapour pressure, it was common knowledge that it does not take part in gas-particle partitioning and therefore has no impact on direct SOA formation. However, the Henry's law constant for glyoxal is surprisingly high. This has been explained by the hydration of the aldehyde groups, which means that a species with a lower vapour pressure is produced. Therefore the distribution of glyoxal between gas- and particle phase is atmospherically relevant and the direct contribution of glyoxal to SOA can no longer be neglected. A high salt concentration present in chamber seed aerosols leads to an enhanced glyoxal uptake into the particle. This effect is called "salting-in". The salting effect depends on the composition of the seed aerosol as well as the soluble compound. For very polar compounds, like glyoxal, a "salting-in" is observed[3]. Glyoxal particle formation during a smog chamber campaign at Paul-Scherrer-Institut (PSI) in Switzerland was examined using different seed aerosols such as ammonium sulfate, sodium chloride and sodium nitrate. The aim of this campaign was to investigate Henry's law constants for different seed aerosols. During the campaign filter samples were taken to investigate the amount of glyoxal in the particle phase. After filter extraction, the analyte was derivatized and measured using UHPLC

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

    SciTech Connect

    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.

    2010-03-15

    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

  14. Earth Science With the Stratospheric Aerosol and Gas Experiment III (SAGE III) on the International Space Station

    NASA Technical Reports Server (NTRS)

    Zawodny, Joe; Vernier, Jean-Paul; Thomason, Larry; Roell, Marilee; Pitts, Mike; Moore, Randy; Hill, Charles; Flittner, David; Damadeo, Rob; Cisewski, Mike

    2015-01-01

    The Stratospheric Aerosol and Gas Experiment (SAGE) III is the fourth generation of solar occultation instruments operated by NASA, the first coming under a different acronym, to investigate the Earth's upper atmosphere. Three flight-ready SAGE III instruments were built by Ball Aerospace in the late 1990s, with one launched aboard the former Russian Aviation and Space Agency (now known as Roskosmos) Meteor-3M platform on 10 December 2001 (continuing until the platform lost power in 2006). Another of the original instruments was manifested for the ISS in the 2004 time frame, but was delayed because of budgetary considerations. Fortunately, that SAGE III/ISS mission was restarted in 2009 with a major focus upon filling an anticipated gap in ozone and aerosol observation in the second half of this decade. Here we discuss the mission architecture, its implementation, and data that will be produced by SAGE III/ISS, including their expected accuracy and coverage. The 52-degree inclined orbit of the ISS is well-suited for solar occultation and provides near-global observations on a monthly basis with excellent coverage of low and mid-latitudes. This is similar to that of the SAGE II mission (1985-2005), whose data set has served the international atmospheric science community as a standard for stratospheric ozone and aerosol measurements. The nominal science products include vertical profiles of trace gases, such as ozone, nitrogen dioxide and water vapor, along with multi-wavelength aerosol extinction. Though in the visible portion of the spectrum the brightness of the Sun is one million times that of the full Moon, the SAGE III instrument is designed to cover this large dynamic range and also perform lunar occultations on a routine basis to augment the solar products. The standard lunar products were demonstrated during the SAGE III/M3M mission and include ozone, nitrogen dioxide & nitrogen trioxide. The operational flexibility of the SAGE III spectrometer accomplishes

  15. Current and future advances in optical multiangle remote sensing of aerosols and clouds based on Terra/MISR experience

    NASA Astrophysics Data System (ADS)

    Diner, David J.; Davies, Roger; Kahn, Ralph; Martonchik, John; Gaitley, Barbara; Davis, Ab

    2006-12-01

    Through acquisition of well-calibrated near-nadir and oblique-angle imagery (0° - 70° zenith angles) at moderately high spatial resolution (275 m - 1.1 km), the Multi-angle Imaging SpectroRadiometer (MISR) experiment aboard NASA's Terra satellite has taken atmospheric remote sensing in new directions. Retrieval algorithms that were largely conceptual prior to Terra launch in 1999 have led to publicly available aerosol and cloud products with direct application to global climate and particulate air quality research. Automated algorithms making use of stereoscopic parallax, time lapse among the nine angular views, and the variation in radiance with view angle, scattering angle, and wavelength (446-866 nm) make possible unique data sets including geometric cloud and aerosol plume heights derived independently of emissivity or temperature assumptions; height-resolved cloud-tracked winds; and aerosol optical depth and particle type over a wide variety of surfaces including bright desert source regions. To illustrate these capabilities, examples of regional and global MISR data products, quantitative evaluations of product accuracies based on comparisons with independent data sources, and time series showing seasonal and interannual variations are presented here. Future sensor improvements aimed at building upon MISR heritage, including expanding the spectral coverage to ultraviolet and shortwave infrared wavelengths, adding polarization channels, and widening the sensor swath, are also discussed.

  16. One Year of Doppler Lidar Observations Characterizing Boundary Layer Wind, Turbulence, and Aerosol Structure During the Indianapolis Flux Experiment

    NASA Astrophysics Data System (ADS)

    Hardesty, R. M.; Brewer, A.; Shepson, P. B.; Cambaliza, M. O. L.; Salmon, O. E.; Heimburger, A. M. F.; Davis, K. J.; Lauvaux, T.; McGowan, L. E.; Miles, N. L.; Richardson, S.; Sarmiento, D. P.; Karion, A.; Sweeney, C.; Iraci, L. T.; Hillyard, P. W.; Podolske, J. R.; Gurney, K. R.; Razlivanov, I. N.; Song, Y.; Turnbull, J. C.; Whetstone, J. R.; Possolo, A.; Prasad, K.

    2014-12-01

    The Indianapolis Flux Experiment (INFLUX) is aimed at improving methods for estimation of greenhouse gas emissions at urban scales. INFLUX observational components include several-times-per-month aircraft measurements of gas concentrations and meteorological parameters, as well as a number of towers observing CO2, CH4, and CO and a single continuously operating Doppler lidar to estimate wind, turbulence and aerosol structure in the boundary layer. The observations are used to develop top-down emissions estimates from the aircraft measurements and as input to inversion models. The Doppler lidar provides information on boundary layer structure for both the aircraft and inversion studies. A commercial Doppler lidar characterized by low pulse energy and high pulse repetition rate has operated for well over a year at a site NE of downtown Indianapolis. The lidar produces profiles of horizontal wind speed, vertical velocity variance, and aerosol structure two to three times per hour. These data are then used to investigate boundary layer mixing and thickness and horizontal transport as inputs for the flux calculations. During its one year deployment the lidar generally operated reliably with few outages. Comparisons with aircraft spirals over the site and with the NOAA High Resolution research Doppler lidar deployed to Indianapolis for one month during May, 2014, were used to assess the performance of the INFLUX lidar. Measurements agreed quite well when aerosol loading was sufficient for lidar observations throughout the boundary layer. However, low aerosol loading during some periods limited the range of the lidar and precluded characterization of the full boundary layer. We present an overall assessment of the commercial Doppler lidar for providing the needed information on boundary layer structure for emission estimations, and show variability of the boundary layer observations over diurnal, seasonal, and annual cycles. Recommendations on system design changes to

  17. Aerosol and Cloud Properties during the Cloud Cheju ABC Plume -Asian Monsoon Experiment (CAPMEX) 2008: Linking between Ground-based and UAV Measurements

    NASA Astrophysics Data System (ADS)

    Kim, S.; Yoon, S.; Venkata Ramana, M.; Ramanathan, V.; Nguyen, H.; Park, S.; Kim, M.

    2009-12-01

    Cheju Atmospheric Brown Cloud (ABC) Plume-Monsoon Experiment (CAPMEX), comprehsensive ground-based measurements and a series of data-gathering flights by specially equipped autonomous unmanned aerial vehicles (AUAVs) for aerosol and cloud, had conducted at Jeju (formerly, Cheju), South Korea during August-September 2008, to improve our understanding of how the reduction of anthropogenic emissions in China (so-called “great shutdown” ) during and after the Summer Beijing Olympic Games 2008 effcts on the air quliaty and radiation budgets and how atmospheric brown clouds (ABCs) influences solar radiation budget off Asian continent. Large numbers of in-situ and remote sensing instruments at the Gosan ABC observatory and miniaturized instruments on the aircraft measure a range of properties such as the quantity of soot, size-segregated aerosol particle numbers, total particle numbers, size-segregated cloud droplet numbers (only AUAV), aerosol scattering properties (only ground), aerosol vertical distribution, column-integrated aerosol properties, and meteorological variables. By integrating ground-level and high-elevation AUAV measurements with NASA-satellite observations (e.g., MODIS, CALIPSO), we investigate the long range transport of aerosols, the impact of ABCs on clouds, and the role of biogenic and anthropogenic aerosols on cloud condensation nuclei (CCN). In this talk, we will present the results from CAPMEX focusing on: (1) the characteristics of aerosol optical, physical and chemical properties at Gosan observatory, (2) aerosol solar heating calculated from the ground-based micro-pulse lidar and AERONET sun/sky radiometer synergy, and comparison with direct measurements from UAV, and (3) aerosol-cloud interactions in conjunction with measurements by satellites and Gosan observatory.

  18. Measurements of aerosol distributions and properties from Airborne High Spectral Resolution Lidar and DRAGON during the DISCOVER-AQ California Experiment (Invited)

    NASA Astrophysics Data System (ADS)

    Ferrare, R. A.; Burton, S. P.; Scarino, A. J.; Hostetler, C. A.; Hair, J. W.; Rogers, R. R.; Mueller, D.; Chemyakin, E.; Cook, A. L.; Harper, D. B.; Hare, R.; Holben, B. N.; Schafer, J.; Anderson, B. E.; Sawamura, P.

    2011-12-01

    The new NASA Langley Research Center airborne High Spectral Resolution Lidar-2 (HSRL-2) was deployed from the NASA Langley King Air aircraft for the DISCOVER-AQ (Deriving Information on Surface Conditions from COlumn and VERtically Resolved Observations Relevant to Air Quality) and DRAGON experiments that occurred over the San Joaquin Valley during January and February, 2013. The HSRL-2, which is the world's first airborne multiwavelength HSRL, measures aerosol extinction at 355 and 532 nm via the HSRL technique, as well as aerosol backscatter and depolarization at 355, 532, and 1064 nm. Additional HSRL-2 data products include aerosol type, mixed layer depth, and range-resolved aerosol microphysical parameters (e.g., effective radius, index of refraction, single scatter albedo, and concentration). During this mission, the King Air flights and HSRL-2 measurements were acquired over the DRAGON network and long-term AERONET sites and were closely coordinated with flights of the NASA P-3 aircraft that carried a suite of in situ aerosol instruments. In this presentation, we discuss how the HSRL-2 and DRAGON observations have been used to examine aerosol optical and microphysical properties as well as spatial and temporal variability. On some days, both HSRL-2 and DRAGON measurements indicated that coarse mode dust contributed a significant fraction of the aerosol optical thickness (AOT); in these cases, HSRL-2 measurements indicated that this depolarizing layer was located at the top of the boundary layer. We discuss differences in the aerosol properties between two episodes of high surface PM2.5 concentrations as revealed by the HSRL-2 and DRAGON measurements. Both the HSRL-2 and DRAGON measurements reveal considerable day-to-day spatial variability in the aerosol distributions across the valley. The HSRL-2 measurements also show variability in the daily evolution of the vertical distribution of aerosols.

  19. Measurements of aerosol distributions and properties from Airborne High Spectral Resolution Lidar and DRAGON during the DISCOVER-AQ California Experiment (Invited)

    NASA Astrophysics Data System (ADS)

    Ferrare, R. A.; Burton, S. P.; Scarino, A. J.; Hostetler, C. A.; Hair, J. W.; Rogers, R. R.; Mueller, D.; Chemyakin, E.; Cook, A. L.; Harper, D. B.; Hare, R.; Holben, B. N.; Schafer, J.; Anderson, B. E.; Sawamura, P.

    2013-12-01

    The new NASA Langley Research Center airborne High Spectral Resolution Lidar-2 (HSRL-2) was deployed from the NASA Langley King Air aircraft for the DISCOVER-AQ (Deriving Information on Surface Conditions from COlumn and VERtically Resolved Observations Relevant to Air Quality) and DRAGON experiments that occurred over the San Joaquin Valley during January and February, 2013. The HSRL-2, which is the world's first airborne multiwavelength HSRL, measures aerosol extinction at 355 and 532 nm via the HSRL technique, as well as aerosol backscatter and depolarization at 355, 532, and 1064 nm. Additional HSRL-2 data products include aerosol type, mixed layer depth, and range-resolved aerosol microphysical parameters (e.g., effective radius, index of refraction, single scatter albedo, and concentration). During this mission, the King Air flights and HSRL-2 measurements were acquired over the DRAGON network and long-term AERONET sites and were closely coordinated with flights of the NASA P-3 aircraft that carried a suite of in situ aerosol instruments. In this presentation, we discuss how the HSRL-2 and DRAGON observations have been used to examine aerosol optical and microphysical properties as well as spatial and temporal variability. On some days, both HSRL-2 and DRAGON measurements indicated that coarse mode dust contributed a significant fraction of the aerosol optical thickness (AOT); in these cases, HSRL-2 measurements indicated that this depolarizing layer was located at the top of the boundary layer. We discuss differences in the aerosol properties between two episodes of high surface PM2.5 concentrations as revealed by the HSRL-2 and DRAGON measurements. Both the HSRL-2 and DRAGON measurements reveal considerable day-to-day spatial variability in the aerosol distributions across the valley. The HSRL-2 measurements also show variability in the daily evolution of the vertical distribution of aerosols.

  20. Aerosol mobility size spectrometer

    DOEpatents

    Wang, Jian; Kulkarni, Pramod

    2007-11-20

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

  1. MELCOR aerosol transport module modification for NSSR-1

    SciTech Connect

    Merrill, B.J.; Hagrman, D.L.

    1996-03-01

    This report describes modifications of the MELCOR computer code aerosol transport module that will increase the accuracy of calculations for safety analysis of the International Thermonuclear Experimental Reactor (ITER). The modifications generalize aerosol deposition models to consider gases other than air, add specialized models for aerosol deposition during high speed gas flows in ducts, and add models for resuspension of aerosols that are entrained in coolants when these coolants flash. Particular attention has been paid to the adhesion of aerosol particles once they are transported to duct walls. The results of calculations with the modified models have been successfully compared to data from Light Water Reactor Aerosol Containment Experiments (LACE) conducted by an international consortium at Hanford, Washington.

  2. Long-term safety of a non-chlorofluorocarbon-containing triamcinolone acetonide inhalation aerosol in patients with asthma. Azmacort HFA Study Group.

    PubMed

    Nelson, H S; Kane, R E; Petillo, J; Banerji, D

    2000-04-01

    In response to environmental concerns regarding chlorofluorocarbon (CFC), two new triamcinolone acetonide (TAA) inhalation aerosol (Azmacort Inhalation Aerosol) formulations have been developed using a more environmentally favorable propellant, HFA-134a (1,1,1,2-tetrafluoroethane). This multicenter, open-label study evaluated the safety of switching asthma patients from TAA-CFC to one of two TAA-HFA formulations. After a 2- or 4-week baseline period during which patients received only CFC-containing TAA Inhaler, 552 patients were randomized to receive TAA-HFA 75 or 225 microg for 6 or 12 months. A total of 493 patients completed treatment. Seven patients discontinued because of adverse events and two because of ineffective asthma control. The incidence of adverse events was similar in the two treatment groups, and most events were mild to moderate in severity and were not considered related to study medication. No clinically relevant suppression of the hypophyseal-pituitary-adrenal (HPA) axis was observed. Pulmonary function tests were not adversely affected by use of either study medication, and improvements were noted in forced expiratory volume in 1 sec (FEV1) and forced expiratory flow between 25% and 75% of forced vital capacity (FEF25%-75%) throughout the course of treatment. This study confirms that TAA-HFA provides effective, long-term asthma control and can safely be substituted for the currently marketed CFC-containing TAA product. PMID:10805203

  3. Attachment of radon progeny to cigarette-smoke aerosols

    SciTech Connect

    Biermann, A.H.; Sawyer, S.R.

    1995-05-01

    The daughter products of radon gas are now recognized as a significant contributor to radiation exposure to the general public. It is also suspected that a synergistic effect exists with the combination cigarette smoking and radon exposure. We have conducted an experimental investigation to determine the physical nature of radon progeny interactions with cigarette smoke aerosols. The size distributions of the aerosols are characterized and attachment rates of radon progeny to cigarette-smoke aerosols are determined. Both the mainstream and sidestream portions of the smoke aerosol are investigated. Unattached radon progeny are very mobile and, in the presence of aerosols, readily attach to the particle surfaces. In this study, an aerosol chamber is used to contain the radon gas, progeny and aerosol mixture while allowing the attachment process to occur. The rate of attachment is dependent on the size distribution, or diffusion coefficient, of the radon progeny as well as the aerosol size distribution. The size distribution of the radon daughter products is monitored using a graded-screen diffusion battery. The diffusion battery also enables separation of the unattached radon progeny from those attached to the aerosol particles. Analysis of the radon decay products is accomplished using alpha spectrometry. The aerosols of interest are size fractionated with the aid of a differential mobility analyzer and cascade impactor. The measured attachment rates of progeny to the cigarette smoke are compared to those found in similar experiments using an ambient aerosol. The lowest attachment coefficients observed, {approximately}10{sup {minus}6} cm{sup 3}/s, occurred for the ambient aerosol. The sidestream and mainstream smoke aerosols exhibited higher attachment rates in that order. The results compared favorably with theories describing the coagulation process of aerosols.

  4. Insights into aerosol formation chemistry from comprehensive gas-phase precursor measurement in the TRAPOZ chamber experiments; an overview

    NASA Astrophysics Data System (ADS)

    Carr, Timo; Wyche, Kevin; Monks, Paul S.; Camredon, Marie; Alam, Mohammed S.; Bloss, William J.; Rickard, Andrew R.

    2010-05-01

    Aerosols have a profound affect on the environment on local, regional and even global levels, with impacts including adverse health effects, (Alfarra, Paulsen et al. 2006) visibility reduction, cloud formation, direct radiative forcing (Charlson, Schwartz et al. 1992) and an important role in influencing the climate due to their contribution to important atmospheric processes (Baltensperger, Kalberer et al. 2005; Alfarra, Paulsen et al. 2006). The Total Radical Production from the OZonolysis of alkenes (TRAPOZ) project was used to study the gas phase and radical chemistry along with secondary organic aerosol (SOA) formation for a number of different alkenes and terpenes. In order to better the scientific knowledge regarding the oxidation mechanisms of terpene and alkene species along with radical and SOA formation, the experiments were conducted under varying conditions controlled and monitored by the EUropean PHOto REactor (EUPHORE) simulation chamber in Valencia, Spain. A vast number of instruments enabled a detailed examination of the chemistry within oxidation of each precursor. However the work here will focus on the results obtained from the University of Leicester Chemical Ionisation Reaction Time-of-Flight Mass Spectrometer (CIR-TOF-MS). With regard to the gas phase chemistry an analysis of the degradation of the precursor Volatile Organic Compounds (VOCs) and evolution of certain gas phase species in each experiment has been presented and discussed.

  5. Aerosol Disinfection Capacity of Slightly Acidic Hypochlorous Acid Water Towards Newcastle Disease Virus in the Air: An In Vivo Experiment.

    PubMed

    Hakim, Hakimullah; Thammakarn, Chanathip; Suguro, Atsushi; Ishida, Yuki; Nakajima, Katsuhiro; Kitazawa, Minori; Takehara, Kazuaki

    2015-12-01

    Existence of bioaerosol contaminants in farms and outbreaks of some infectious organisms with the ability of transmission by air increase the need for enhancement of biosecurity, especially for the application of aerosol disinfectants. Here we selected slightly acidic hypochlorous acid water (SAHW) as a candidate and evaluated its virucidal efficacy toward a virus in the air. Three-day-old conventional chicks were challenged with 25 doses of Newcastle disease live vaccine (B1 strain) by spray with nebulizer (particle size <3 μm in diameter), while at the same time reverse osmosis water as the control and SAHW containing 50 or 100 parts per million (ppm) free available chlorine in pH 6 were sprayed on the treated chicks with other nebulizers. Exposed chicks were kept in separated cages in an isolator and observed for clinical signs. Oropharyngeal swab samples were collected from 2 to 5 days postexposure from each chick, and then the samples were titrated with primary chicken kidney cells to detect the virus. Cytopathic effects were observed, and a hemagglutination test was performed to confirm the result at 5 days postinoculation. Clinical signs (sneezing) were recorded, and the virus was isolated from the control and 50 ppm treatment groups, while no clinical signs were observed in and no virus was isolated from the 100 ppm treatment group. The virulent Newcastle disease virus (NDV) strain Sato, too, was immediately inactivated by SAHW containing 50 ppm chlorine in the aqueous phase. These data suggest that SAHW containing 100 ppm chlorine can be used for aerosol disinfection of NDV in farms. PMID:26629621

  6. Chemistry of organic aerosol formation in urban atmospheres. Final report

    SciTech Connect

    Seinfeld, J.H.; Flagan, R.C.

    1994-04-04

    Aerosol formation from the photooxidation of A-pinene/NOx and B-pinene/NOx mixtures has been investigated in a series of outdoor smog chamber experiments. Both hydrocarbons are potent aerosol formers and in areas containing significant vegetation, terpenes are estimated to be a significant contributor to secondary organic aerosol formation. To model organic aerosol formation, estimates of the vapor pressures of the condensable species are needed. To measure the vapor pressures of the low volatility species characteristic of organic aerosols the Tandem Differential Mobility Analyzer (TDMA) method introduced by Liu and McMurray has been further developed for this task. Initial experiments with compounds of known vapor pressure confirm the usefulness of the method.

  7. Morphological characterization of soot aerosol particles during LACIS Experiment in November (LExNo)

    NASA Astrophysics Data System (ADS)

    Kiselev, A.; Wennrich, C.; Stratmann, F.; Wex, H.; Henning, S.; Mentel, T. F.; Kiendler-Scharr, A.; Schneider, J.; Walter, S.; Lieberwirth, I.

    2010-06-01

    Combined mobility and aerodynamic measurements were used to characterize the morphology of soot particles in an experimental campaign on the hygroscopic growth and activation of an artificial biomass burning aerosol. A custom-made, single-stage low-pressure impactor and two aerosol mass spectrometers (AMS) operating in the free molecular regime were used to measure the vacuum aerodynamic diameter of mobility-selected artificial soot particles that were produced in a spark discharge generator and then modified by condensation of ammonium hydrogen sulfate or levoglucosan as a coating to change their hydroscopic activity. Transmission electron microscope images revealed a relationship between the electrical mobility diameter and the diameter of the enveloping sphere, thus enabling evaluation of the effective density of soot agglomerates. A fractal description of the morphology of the soot aggregates allowed for evaluation of the average mass of the hygroscopic material per particle. The average mass of the hygroscopic material per particle was also measured directly with the two AMS instruments, and the agreement between the two methods was found satisfactory. This tandem approach allows detection of small changes in the particle effective density and morphology caused by condensation of organic material.

  8. Wavelength Dependence of the Absorption of Black Carbon Particles: Predictions and Results from the TARFOX Experiment and Implications for the Aerosol Single Scattering Albedo

    NASA Technical Reports Server (NTRS)

    Bergstrom, Robert W.; Russell, Philip B.; Hignett, Phillip

    2002-01-01

    Measurements are presented of the wavelength dependence of the aerosol absorption coefficient taken during the Tropical Aerosol Radiative Forcing Observational Experiment (TARFOX) over the northern Atlantic. The data show an approximate lamda(exp -1) variation between 0.40 and 1.0 micrometers. The theoretical basis of the wavelength variation of the absorption of solar radiation by elemental carbon [or black carbon (BC)] is explored. For a wavelength independent refractive index the small particle absorption limit simplifies to a lambda(exp -1) variation in relatively good agreement with the data. This result implies that the refractive indices of BC were relatively constant in this wavelength region, in agreement with much of the data on refractive indices of BC. However, the result does not indicate the magnitude of the refractive indices. The implications of the wavelength dependence of BC absorption for the spectral behavior of the aerosol single scattering albedo are discussed. It is shown that the single scattering albedo for a mixture of BC and nonabsorbing material decreases with wavelength in the solar spectrum (i.e., the percentage amount of absorption increases). This decease in the single scattering albedo with wavelength for black carbon mixtures is different from the increase in single scattering allied for most mineral aerosols (dusts). This indicates that, if generally true, the spectral variation of the single- scattering albedo can be used to distinguish aerosol types. It also highlights the importance of measurements of the spectral variation of the aerosol absorption coefficient and single scattering albedo.

  9. Carbonaceous aerosol characteristics over a Pinus taeda plantation: Results from the CELTIC experiment

    NASA Astrophysics Data System (ADS)

    Geron, Chris

    2011-01-01

    Carbonaceous particles smaller than 2.5 μm aerodynamic diameter (PM 2.5) were collected in July, 2003 over a Loblolly Pine plantation at Duke Forest, NC during the Chemical Emission, Loss, Transformation and Interactions within Canopies (CELTIC) field study. Organic (OC) and elemental (EC) carbon in PM 2.5 ranged from 1.4-6.3 and 0.08-0.41 μg C m -3, respectively, and concentrations measured above and below the pine canopy were in good agreement. Ambient OC was lower (<3 μg C m -3) during cooler periods (daytime maximum temperatures < 28 °C) and for periods following precipitation events, and was higher (>3 μg C m -3) during warm humid periods. Radiocarbon analysis indicates that on average 83% (range 78-91%) of the PM 2.5 carbon was derived from contemporary (biogenic VOC and biomass burning) sources. This is higher than previous estimates from urban and suburban sites, and in good agreement with recently published data from other rural sites throughout the U.S. The estimates of contemporary PM 2.5 carbon may represent a lower limit for this site since the sampler was located above the center of a 30 meter diameter plot fumigated with 200 ppm CO 2 derived from fossil carbon sources. However, this effect is likely to be negligible. The regression relationship between OC/EC ratios and percent biogenic carbon in aerosol is very similar to those observed in recent summertime data from Tennessee and Florida. However, our values for both OC/EC and percent biogenic carbon are higher than those observed in the latter studies, likely due to the more rural character of the site. Simple box model estimates indicate that biogenic VOC (BVOC) emissions measured at the site provide sufficient reactive carbon sources to account for the observed levels of aerosol biogenic carbon. The magnitude and temporal pattern in the box model secondary organic aerosol estimates correlate well with the ambient aerosol carbon measurements. The model estimates of the relative contribution

  10. The technical basis for air pathway assessment of resuspended radioactive aerosols: LLNL experiences at seven sites around the world

    SciTech Connect

    Shinn, J.H.

    1993-09-01

    There is a large uncertainty in quantifying the inhalation pathway and the aerosol emission rate in human health assessments of radioactive-contamination sites. The need for site-specific assessments led to formation of our team of specialists at LLNL, who have participated in numerous field campaigns around the world. Our goal was to obtain all the information necessary for determining potential human exposures and to estimate source terms for turbulent transport of the emissions during both normal and disturbed soil conditions. That is, measurements were made of the key variables to quantify the suspended aerosols at the actual contamination sites, but different scenarios for habitation, site management, and site cleanup were included. The most notable locations of these site-investigations were the Marshall Islands (Bikini, Enewetak, and Rongelap), Nevada Test Site (GMX, Little Feller, Palanquin, and Plutonium Valley), Tonopah (Nevada--site of Roller Coaster), Savannah River Lab (South Carolina--H-Area site), Johnston Island (cleanup of rocket-impact site), Chernobyl (Ukraine--grass field end sandy beach sites near Nuclear Power Plant Unit 4), and Palomares (Spain--site of aircraft accident). This discussion will review the variables quantified, methods developed, general results, uncertainty of estimations, and recommendations for future research that are a result of our experience in these field studies.

  11. Constraining Aerosol Optical Models Using Ground-Based, Collocated Particle Size and Mass Measurements in Variable Air Mass Regimes During the 7-SEAS/Dongsha Experiment

    NASA Technical Reports Server (NTRS)

    Bell, Shaun W.; Hansell, Richard A.; Chow, Judith C.; Tsay, Si-Chee; Wang, Sheng-Hsiang; Ji, Qiang; Li, Can; Watson, John G.; Khlystov, Andrey

    2012-01-01

    During the spring of 2010, NASA Goddard's COMMIT ground-based mobile laboratory was stationed on Dongsha Island off the southwest coast of Taiwan, in preparation for the upcoming 2012 7-SEAS field campaign. The measurement period offered a unique opportunity for conducting detailed investigations of the optical properties of aerosols associated with different air mass regimes including background maritime and those contaminated by anthropogenic air pollution and mineral dust. What appears to be the first time for this region, a shortwave optical closure experiment for both scattering and absorption was attempted over a 12-day period during which aerosols exhibited the most change. Constraints to the optical model included combined SMPS and APS number concentration data for a continuum of fine and coarse-mode particle sizes up to PM2.5. We also take advantage of an IMPROVE chemical sampler to help constrain aerosol composition and mass partitioning of key elemental species including sea-salt, particulate organic matter, soil, non sea-salt sulphate, nitrate, and elemental carbon. Our results demonstrate that the observed aerosol scattering and absorption for these diverse air masses are reasonably captured by the model, where peak aerosol events and transitions between key aerosols types are evident. Signatures of heavy polluted aerosol composed mostly of ammonium and non sea-salt sulphate mixed with some dust with transitions to background sea-salt conditions are apparent in the absorption data, which is particularly reassuring owing to the large variability in the imaginary component of the refractive indices. Extinctive features at significantly smaller time scales than the one-day sample period of IMPROVE are more difficult to reproduce, as this requires further knowledge concerning the source apportionment of major chemical components in the model. Consistency between the measured and modeled optical parameters serves as an important link for advancing remote

  12. Origin of surface and columnar Indian Ocean Experiment (INDOEX) aerosols using source- and region-tagged emissions transport in a general circulation model - article no. D24211

    SciTech Connect

    Verma, S.; Venkataraman, C.; Boucher, O.

    2008-12-15

    We study the relative influence of aerosols emitted from different sectors and geographical regions on aerosol loading in south Asia. Sectors contributing aerosol emissions include biofuel and fossil fuel combustion, open biomass burning, and natural sources. Geographical regions include India, southeast Asia, east Asia, Africa-west Asia, and the rest of the world. Simulations of the Indian Ocean Experiment (INDOEX), from January to March 1999, are made in the general circulation model of Laboratoire de Meteorologie Dynamique (LMD-ZT GCM) with emissions tagged by sector and geographical region. Anthropogenic emissions dominate (54-88%) the predicted aerosol optical depth (AOD) over all the receptor regions. Among the anthropogenic sectors, fossil fuel combustion has the largest overall influence on aerosol loading, primarily sulfate, with emissions from India (50-80%) and rest of the world significantly influencing surface concentrations and AOD. Biofuel combustion has a significant influence on both the surface and columnar black carbon (BC) in particular over the Indian subcontinent and Bay of Bengal with emissions largely from the Indian region (60-80%). Open biomass burning emissions influence organic matter (OM) significantly, and arise largely from Africa-west Asia. The emissions from Africa-west Asia affect the carbonaceous aerosols AOD in all receptor regions, with their largest influence (AOD-BC: 60%; and AOD-OM: 70%) over the Arabian Sea. Among Indian regions, the Indo-Gangetic Plain is the largest contributor to anthropogenic surface mass concentrations and AOD over the Bay of Bengal and India. Dust aerosols are contributed mainly through the long-range transport from Africa-west Asia over the receptor regions. Overall, the model estimates significant intercontinental incursion of aerosol, for example, BC, OM, and dust from Africa-west Asia and sulfate from distant regions (rest of the world) into the INDOEX domain.

  13. Aerosol phase transformation in the atmosphere

    SciTech Connect

    Tang, I.N.; Munkelwitz, H.R.

    1992-09-01

    Ambient aerosols are frequently composed of hygroscopic inorganic salts such as chlorides, sulfates and nitrates in either pure or mixed forms. Such inorganic salt aerosols exhibit the properties of deliquescence and efflorescence in air. The phase transformation from a solid particle to a saline droplet usually occurs spontaneously when atmospheric relative humidity reaches a level specific to the chemical composition of the aerosol particle. Conversely, when relative humidity decreases and becomes low enough, a saline droplet will evaporate and suddenly crystallize, expelling all its water content. Information on the composition and temperature dependence of these properties is required in mathematical models for describing the dynamic and transport behavior of ambient aerosols. Experiments are carried out in the temperature range 5--35{degrees}C, using single particles individually suspended in an electrodynamic cell that can be evacuated and back filled with water vapor. The phase transformation of the aerosol particle is monitored by laser light scattering and the relative humidity at the transition point is determined by directly measuring the water vapor pressure in the cell. Results are obtained for particles containing either a single salt or a preselected mixture of NaCl, KCl, NaNO{sub 3}, Na{sub 2}SO{sub 4} and (NH{sub 4}){sub 2}SO{sub 4}, which are common constituents of ambient aerosols. A theoretical model on the composition and temperature dependence of the deliquescence properties is developed for single and two-salt aerosol systems.

  14. Protection factor for N95 filtering facepiece respirators exposed to laboratory aerosols containing different concentrations of nanoparticles.

    PubMed

    Rengasamy, Samy; Walbert, Gary; Newcomb, William; Coffey, Christopher; Wassell, James Terrence; Szalajda, Jonathan

    2015-04-01

    A previous study used a PortaCount Plus to measure the ratio of particle concentrations outside (C out) to inside (C in) of filtering facepiece respirators (FFRs) worn by test subjects and calculated the total inward leakage (TIL) (C in/C out) to evaluate the reproducibility of the TIL test method between two different National Institute for Occupational Safety and Health laboratories (Laboratories 1 and 2) at the Pittsburgh Campus. The purpose of this study is to utilize the originally obtained PortaCount C out/C in ratio as a measure of protection factor (PF) and evaluate the influence of particle distribution and filter efficiency. PFs were obtained for five N95 model FFRs worn by 35 subjects for three donnings (5 models × 35 subjects × 3 donnings) for a total of 525 tests in each laboratory. The geometric mean of PFs, geometric standard deviation (GSD), and the 5th percentile values for the five N95 FFR models were calculated for the two laboratories. Filter efficiency was obtained by measuring the penetration for four models (A, B, C, and D) against Laboratory 2 aerosol using two condensation particle counters. Particle size distribution, measured using a Scanning Mobility Particle Sizer, showed a mean count median diameter (CMD) of 82 nm in Laboratory 1 and 131 nm in Laboratory 2. The smaller CMD showed relatively higher concentration of nanoparticles in Laboratory 1 than in Laboratory 2. Results showed that the PFs and 5th percentile values for two models (B and E) were larger than other three models (A, C, and D) in both laboratories. The PFs and 5th percentile values of models B and E in Laboratory 1 with a count median diameter (CMD) of 82 nm were smaller than in Laboratory 2 with a CMD of 131 nm, indicating an association between particle size distribution and PF. The three lower efficiency models (A, C, and D) showed lower PF values than the higher efficiency model B showing the influence of filter efficiency on PF value. Overall, the data show that

  15. Protection Factor for N95 Filtering Facepiece Respirators Exposed to Laboratory Aerosols Containing Different Concentrations of Nanoparticles

    PubMed Central

    Rengasamy, Samy; Walbert, Gary; Newcomb, William; Coffey, Christopher; Wassell, James Terrence; Szalajda, Jonathan

    2015-01-01

    A previous study used a PortaCount Plus to measure the ratio of particle concentrations outside (Cout) to inside (Cin) of filtering facepiece respirators (FFRs) worn by test subjects and calculated the total inward leakage (TIL) (Cin/Cout) to evaluate the reproducibility of the TIL test method between two different National Institute for Occupational Safety and Health laboratories (Laboratories 1 and 2) at the Pittsburgh Campus. The purpose of this study is to utilize the originally obtained PortaCount Cout/Cin ratio as a measure of protection factor (PF) and evaluate the influence of particle distribution and filter efficiency. PFs were obtained for five N95 model FFRs worn by 35 subjects for three donnings (5 models × 35 subjects × 3 donnings) for a total of 525 tests in each laboratory. The geometric mean of PFs, geometric standard deviation (GSD), and the 5th percentile values for the five N95 FFR models were calculated for the two laboratories. Filter efficiency was obtained by measuring the penetration for four models (A, B, C, and D) against Laboratory 2 aerosol using two condensation particle counters. Particle size distribution, measured using a Scanning Mobility Particle Sizer, showed a mean count median diameter (CMD) of 82 nm in Laboratory 1 and 131 nm in Laboratory 2. The smaller CMD showed relatively higher concentration of nanoparticles in Laboratory 1 than in Laboratory 2. Results showed that the PFs and 5th percentile values for two models (B and E) were larger than other three models (A, C, and D) in both laboratories. The PFs and 5th percentile values of models B and E in Laboratory 1 with a count median diameter (CMD) of 82 nm were smaller than in Laboratory 2 with a CMD of 131 nm, indicating an association between particle size distribution and PF. The three lower efficiency models (A, C, and D) showed lower PF values than the higher efficiency model B showing the influence of filter efficiency on PF value. Overall, the data show that

  16. An overview of the Ice Nuclei Research Unit Jungfraujoch/Cloud and Aerosol Characterization Experiment 2013 (INUIT-JFJ/CLACE-2013)

    NASA Astrophysics Data System (ADS)

    Schneider, Johannes

    2014-05-01

    Ice formation in mixed phase tropospheric clouds is an essential prerequisite for the formation of precipitation at mid-latitudes. Ice formation at temperatures warmer than -35°C is only possible via heterogeneous ice nucleation, but up to now the exact pathways of heterogeneous ice formation are not sufficiently well understood. The research unit INUIT (Ice NUcleation research unIT), funded by the Deutsche Forschungsgemeinschaft (DFG FOR 1525) has been established in 2012 with the objective to investigate heterogeneous ice nucleation by combination of laboratory studies, model calculation and field experiments. The main field campaign of the INUIT project (INUIT-JFJ) was conducted at the High Alpine Research Station Jungfraujoch (Swiss Alps, 3580 m asl) during January and February 2013, in collaboration with several international partners in the framework of CLACE2013. The instrumentation included a large set of aerosol chemical and physical analysis instruments (particle counters, particle sizers, particle mass spectrometers, cloud condensation nuclei counters, ice nucleus counters etc.), that were operated inside the Sphinx laboratory and sampled in mixed phase clouds through two ice selective inlets (Ice-CVI, ISI) as well as through a total aerosol inlet that was used for out-of-cloud aerosol measurements. Besides the on-line measurements, also samples for off-line analysis (ESEM, STXM) have been taken in and out of clouds. Furthermore, several cloud microphysics instruments were operated outside the Sphinx laboratory. First results indicate that a large fraction of ice residues sampled from mixed phase clouds contain organic material, but also mineral dust. Soot and lead were not found to be enriched in ice residues. The concentration of heterogeneous ice nuclei was found to be variable (ranging between < 1 and > 100 per liter) and to be strongly dependent on the operating conditions of the respective IN counter. The number size distribution of ice residues

  17. Modeling the organic aerosol fraction within the Mexico City basin during the MILAGRO field experiment

    NASA Astrophysics Data System (ADS)

    Hodzic, A.; Jimenez, J. L.; Madronich, S.; Aiken, A. C.; Bessagnet, B.; Fast, J.; Lamarque, J. F.; Onasch, T. B.; Roux, G.; Ulbrich, I. M.

    2009-04-01

    The meso-scale chemistry-transport model CHIMERE is used to asses our understanding of major sources and formation processes leading to a fairly abundant fraction of organic aerosols (OA, including primary OA (POA) and secondary OA (SOA)) observed in Mexico City during the MILAGRO field project (March 2006). Chemical analysis of submicron aerosols from aerosol mass spectrometers (AMS) indicate that carbonaceous particles found in the Mexico City basin have a large fraction of oxygenated organic species (OOA) which show strong correspondence with SOA, and that their production actively continues downwind of the city. The SOA formation is modeled according to the first-generation oxidation of anthropogenic (i.e. aromatics, alkanes) and biogenic (i.e. monoterpenes and isoprene) precursors and their partitioning into both organic and aqueous phases. The near-surface model evaluation shows that predicted OA correlates reasonably well with measurements during the campaign, however it remains a factor of 2-3 lower than the measured TOA. One of the reasons for this large gap is the inability of the model to simulate TOA peaks associated with the biomass burning events suggesting that near-city fires are not correctly represented in the emissions inventory (most likely too small to be detected by satellites). Fairly good agreement is found between observed and predicted POA within the city indicating that primary emissions are reasonable. Consistent with previous studies in Mexico City, large discrepancies are found for SOA species characterized by a factor of 5-10 model underestimate. When only anthropogenic SOA precursors were considered, the model was able to reproduce the sharp increase in SOA concentrations during the late morning at both urban and near-urban locations. However, predicted SOA concentrations were unrealistically low when photochemistry was not active, especially overnight. These discrepancies were not significantly reduced when greatly enhanced

  18. A comparison of Solar Mesosphere Explorer and Stratosphere Aerosol and Gas Experiment II ozone densities near the stratopause

    NASA Technical Reports Server (NTRS)

    Rusch, D. W.; Clancy, R. T.; Mccormick, M. P.; Zawodny, J. M.

    1990-01-01

    Ozone measurements made by the SME UV Spectrometer and the Stratosphere Aerosol and Gas Experiment II (SAGE II) spectometer are compared at 1.0 mbar for the time period from October 1984 to December 1986, using a model of the diurnal variation of ozone to correct for the difference in local times of the two measurements. The absolute values of the ozone mixing ratio measured by the two spectrometers were found to agree to better than 5 percent, with no significant divergence between the instruments. It is concluded that, since the SAGE II data are not dependent on the absolute calibration of the instrument, these data can be used as time-dependent 'ground truth' measurements for comparisons with other instruments.

  19. Overview of the Stratospheric Aerosol and Gas Experiment II water vapor observations - Method, validation, and data characteristics

    NASA Technical Reports Server (NTRS)

    Rind, D.; Chiou, E.-W.; Chu, W.; Oltmans, S.; Lerner, J.; Larsen, J.; Mccormick, M. P.; Mcmaster, L.

    1993-01-01

    Results are presented of water vapor observations in the troposphere and stratosphere performed by the Stratospheric Aerosol and Gas Experiment II solar occultation instrument, and the analysis procedure, the instrument errors, and data characteristics are discussed. The results are compared with correlative in situ measurements and other satellite data. The features of the data set collected between 1985 and 1989 include an increase in middle- and upper-tropospheric water vapor during northern hemisphere summer and autumn; minimum water vapor values of 2.5-3 ppmv in the tropical lower stratosphere; slowly increasing water vapor values with altitude in the stratosphere, reaching 5-6 ppmv or greater near the stratopause; extratropical values with minimum profile amounts occurring above the conventionally defined tropopause; and higher extratropical than tropical water vapor values throughout the stratosphere except in locations of possible polar stratospheric clouds.

  20. Airborne Lidar measurements of aerosols, mixed layer heights, and ozone during the 1980 PEPE/NEROS summer field experiment

    NASA Technical Reports Server (NTRS)

    Browell, E. V.; Shipley, S. T.; Butler, C. F.; Ismail, S.

    1985-01-01

    A detailed summary of the NASA Ultraviolet Differential Absorption Lidar (UV DIAL) data archive obtained during the EPA Persistent Elevated Pollution Episode/Northeast Regional Oxidant Study (PEPE/NEROS) Summer Field Experiment Program (July through August 1980) is presented. The UV dial data set consists of remote measurements of mixed layer heights, aerosol backscatter cross sections, and sequential ozone profiles taken during 14 long-range flights onboard the NASA Wallops Flight Center Electra aircraft. These data are presented in graphic and tabular form, and they have been submitted to the PEPE/NEROS data archive on digital magnetic tape. The derivation of mixing heights and ozone profiles from UV Dial signals is discussed, and detailed intercomparisons with measurements obtained by in situ sensors are presented.

  1. Automated nuclear material recovery and decontamination of large steel dynamic experiment containers

    SciTech Connect

    Dennison, D.K.; Gallant, D.A.; Nelson, D.C.; Stovall, L.A.; Wedman, D.E.

    1999-03-01

    A key mission of the Los Alamos National Laboratory (LANL) is to reduce the global nuclear danger through stockpile stewardship efforts that ensure the safety and reliability of nuclear weapons. In support of this mission LANL performs dynamic experiments on special nuclear materials (SNM) within large steel containers. Once these experiments are complete, these containers must be processed to recover residual SNM and to decontaminate the containers to below low level waste (LLW) disposal limits which are much less restrictive for disposal purposes than transuranic (TRU) waste limits. The purpose of this paper is to describe automation efforts being developed by LANL for improving the efficiency, increasing worker safety, and reducing worker exposure during the material cleanout and recovery activities performed on these containers.

  2. Direct containment heating experiments in Zion Nuclear Power Plant geometry using prototypic materials

    SciTech Connect

    Binder, J.L.; McUmber, L.M.; Spencer, B.W.

    1993-12-31

    Direct Containment Heating (DCH) experiments have been completed which utilize prototypic core materials. The experiments reported on here are a continuation of the Integral Effects Testing (IET) DCH program. The experiments incorporated a 1/40 scale model of the Zion Nuclear Power Plant containment structures. The model included representations of the primary system volume, RPV lower head, cavity and instrument tunnel, and the lower containment structures. The experiments were steam driven. Iron-alumina thermite with chromium was used as a core melt stimulant in the earlier IET experiments. These earlier IET experiments at Argonne National Laboratory (ANL) and Sandia National Laboratories (SNL) provided useful data on the effect of scale on DCH phenomena; however, a significant question concerns the potential experiment distortions introduced by the use of non-prototypic iron/alumina thermite. Therefore, further testing with prototypic materials has been carried out at ANL. Three tests have been completed, DCH-U1A, U1B and U2. DCH-U1A and U1B employed an inerted containment atmosphere and are counterpart to the IET-1RR test with iron/alumina thermite. DCH-U2 employed nominally the same atmosphere composition of its counterpart iron/alumina test, IET-6. All tests, with prototypic material, have produced lower peak containment pressure rises; 45, 111 and 185 kPa in U1A, U1B and U2, compared to 150 and 250 kPa IET-1RR and 6. Hydrogen production, due to metal-steam reactions, was 33% larger in U1B and U2 compared to IET-1RR and IET-6. The pressurization efficiency was consistently lower for the corium tests compared to the IET tests.

  3. Atmospheric Aerosols

    NASA Technical Reports Server (NTRS)

    Pueschel, R. F.; Lawless, James G. (Technical Monitor)

    1994-01-01

    Aerosols, defined as particles and droplets suspended in air, are always present in the atmosphere. They are part of the earth-atmosphere climate system, because they interact with both incoming solar and outgoing terrestrial radiation. They do this directly through scattering and absorption, and indirectly through effects on clouds. Submicrometer aerosols usually predominate in terms of number of particles per unit volume of air. They have dimensions close to the wavelengths of visible light, and thus scatter radiation from the sun very effectively. They are produced in the atmosphere by chemical reactions of sulfur-, nitrogen- and carbon-containing gases of both natural and anthropogenic origins. Light absorption is dominated by particles containing elemental carbon (soot), produced by incomplete combustion of fossil fuels and by biomass burning. Light-scattering dominates globally, although absorption can be significant at high latitudes, particularly over highly reflective snow- or ice-covered surfaces. Other aerosol substances that may be locally important are those from volcanic eruptions, wildfires and windblown dust.

  4. Ground based characterization of biomass burning aerosols during the South American Biomass Burning Analysis (SAMBBA) field experiment in Brazil during Sept - Oct 2012

    NASA Astrophysics Data System (ADS)

    Artaxo, Paulo; Ferreira de Brito, Joel; Varanda Rizzo, Luciana; Johnson, Ben; Haywood, Jim; Longo, Karla; Freitas, Saulo; Coe, Hugh

    2013-04-01

    Biomass burning is one of the major drivers for atmospheric composition in the Southern hemisphere. In Amazonia, deforestation rates have been steadily decreasing, from 27,000 Km² in 2004 to about 5,000 Km² in 2011. This large reduction (by factor 5) was not followed by similar reduction in aerosol loading in the atmosphere due to the increase in agricultural fires. AERONET measurements from 5 sites show a large year-to year variability due to climatic and socio-economic issues. Besides this strong reduction in deforestation rate, biomass burning emissions in Amazonia increases concentrations of aerosol particles, CO, ozone and other species, and also change the surface radiation balance in a significant way. To complement the long term biomass burning measurements in Amazonia, it was organized in 2012 the intensive campaign of the South American Biomass Burning Analysis (SAMBBA) experiment with an airborne and a ground based components. A sampling site was set up at Porto Velho, with measurements of aerosol size distribution, optical properties such as absorption and scattering at several wavelengths, organic aerosol characterization with an ACSM - Aerosol Chemical Speciation Monitor. CO, CO2 and O3 were also measured to characterize combustion efficiency and photochemical processes. Filters for trace elements measured by XRF and for OC/EC determined using a Sunset instrument were also collected. An AERONET CIMEL sunphotometer was operated in parallel with a multifilter radiometer (MFR). A large data set was collected from August to October 2012. PM2.5 aerosol concentrations up to 250 ug/m3 were measured, with up to 20 ug/m3 of black carbon. Ozone went up to 60 ppb at mid-day in August. At night time ozone was consumed completely most of the time. ACSM shows that more than 85% of the aerosol mass was organic with a clear diurnal pattern. The organic aerosol volatility was very variable depending on the air mass sampled over Porto Velho. Aerosol optical depth at

  5. Airborne LIDAR Measurements of Water Vapor, Ozone, Clouds, and Aerosols in the Tropics Near Central America During the TC4 Experiment

    NASA Technical Reports Server (NTRS)

    Kooi, Susan; Fenn, Marta; Ismail, Syed; Ferrare, Richard; Hair, John; Browell, Edward; Notari, Anthony; Butler, Carolyn; Burton, Sharon; Simpson, Steven

    2008-01-01

    Large scale distributions of ozone, water vapor, aerosols, and clouds were measured throughout the troposphere by two NASA Langley lidar systems on board the NASA DC-8 aircraft as part of the Tropical Composition, Cloud, and Climate Coupling Experiment (TC4) over Central and South America and adjacent oceans in the summer of 2007. Special emphasis was placed on the sampling of convective outflow and transport, sub-visible cirrus clouds, boundary layer aerosols, Saharan dust, volcanic emissions, and urban and biomass burning plumes. This paper presents preliminary results from this campaign, and demonstrates the value of coordinated measurements by the two lidar systems.

  6. Effects of Aerosols over the Indian Ocean

    NASA Technical Reports Server (NTRS)

    2002-01-01

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

  7. Nocturnal Boundary Layer Measurements during the Amazonian Aerosol Characterization Experiment (AMAZE)

    NASA Astrophysics Data System (ADS)

    Tota, J.; Fisch, G.; Santos, R.; Silva Dias, M.

    2009-05-01

    To characterize the Nocturnal Boundary Layer (NBL) hourly profiles of wind, pressure, temperature, humidity and 5 sizes particles concentration, were made by using tethered balloon at INPA tropical Amazon rainforest Reserve (Cuieiras) 100 km northwest from Manaus city. The measurements were made during the wet season March/2008. The NBL height was 100 to 150m, with a very well mixed layer close to surface associate with temperature inversion. The wind profiles shows a very clear low level in two nights, about 500 to 900 m, and, in general, all nights show an stable and cooler air layer close the surface uncoupled with outer residual boundary layer above. At the site a very clear drainage flow from north quadrant down slope eastward quadrant during very the stable cases. This findings is correlates with particles profiles where was commonly trapped by stable layer presenting high concentrations, for all 5 sizes measured, close to the surface at vegetation level and just above it. All nights presents high humidity with fog formation in three cases, associates with temperature below the 23C. The wind speed were very low about 0.5 to calm, in generally associate with drainage flow down hill. The NBL dynamics is a discussion issue associate to the aerosol nocturnal mixing in complex terrain with tall vegetation, the currently AMAZE site case.

  8. Nocturnal Boundary Layer Measurements during the Amazonian Aerosol Characterization Experiment (amaze)

    NASA Astrophysics Data System (ADS)

    Tota, J.; Santos, R.; Fisch, G.; Querino, C.; Silva Dias, M.; Artaxo, P.; Guenther, A.; Martin, S.; Manzi, A.

    2008-12-01

    To characterize the Nocturnal Boundary Layer (NBL) hourly profiles of wind, pressure, temperature, humidity and 5 sizes particles concentration, were made by using tethered balloon at INPA tropical Amazon rainforest Reserve (Cuieiras) 100 km northwest from Manaus city. The measurements were made during the wet season March/2008. The NBL height was 100 to 150m, with a very well mixed layer close to surface associate with temperature inversion. The wind profiles shows a very clear low level in two nights, about 500 to 900 m, and, in general, all nights show an stable and cooler air layer close the surface uncoupled with outer residual boundary layer above. At the site a very clear drainage flow from north quadrant down slope eastward quadrant during very the stable cases. This findings is correlates with particles profiles where was commonly trapped by stable layer presenting high concentrations, for all 5 sizes measured, close to the surface at vegetation level and just above it. All nights presents high humidity with fog formation in three cases, associates with temperature below the 23°C. The wind speed were very low about 0.5 to calm, in generally associate with drainage flow down hill. The NBL dynamics is a discussion issue associate to the aerosol nocturnal mixing in complex terrain with tall vegetation, the currently AMAZE site case.

  9. ABOVE03, The 2003 AIRS BBAERI Ocean Validation Experiment: AIRS Validation and Aerosols

    NASA Astrophysics Data System (ADS)

    McMillan, W. W.; Hoff, R.; Strow, L. L.; Desouza-Machado, S.; Lightner, K.; McCourt, M. L.; Maddy, E.; Kolb, N.; McCann, K.; Comer, J.; Russo, F.; Rutledge, C. K.

    2003-12-01

    From May 28 to July 9, 2003, a complementary set of instruments was deployed to the United States Coast Guard (USCG) Chesapeake Light lighthouse platform to provide correlative measurements characterizing the atmosphere and sea surface over the ocean for validation of NASA's Atmospheric InfraRed Sounder (AIRS) onboard the Aqua satellite. Located 25 km due east of Virginia Beach, VA, Chesapeake Light offers a relatively convenient site for measurements over the ocean while being far enough offshore for water only AIRS fields of view. In addition to the UMBC Baltimore Bomem Atmospheric Emitted Radiance Interferometer (BBAERI), the UMBC Elastic Lidar Facility (ELF), and Vaisala RS-90 rawinsondes used during ABOVE02, we deployed in situ O3 and CO gas analyzers and during the first three weeks, flew 18 ozonesondes in collaboration with Dr. Mike Newchurch, UAH. A total of 140 Vaisala RS-90 radiosondes were launched covering 61 Aqua and 12 Terra overpasses. Preliminary comparisons of ABOVE03 data products to AIRS observations and retrievals will be presented. Particular attention will be paid to both AIRS and ground-based aerosol observations.

  10. Influence of Aerosols on the Shortwave Cloud Radiative Forcing from North Pacific Oceanic Clouds: Results from the Cloud Indirect Forcing Experiment (CIFEX)

    NASA Technical Reports Server (NTRS)

    Wilcox, Eric M.; Roberts, Greg; Ramanathan, V.

    2007-01-01

    Aerosols over the Northeastern Pacific Ocean enhance the cloud drop number concentration and reduce the drop size for marine stratocumulus and cumulus clouds. These microphysical effects result in brighter clouds, as evidenced by a combination of aircraft and satellite observations. In-situ measurements from the Cloud Indirect Forcing Experiment (CIFEX) indicate that the mean cloud drop number concentration in low clouds over the polluted marine boundary layer is greater by 53 cm(sup -3) compared to clean clouds, and the mean cloud drop effective radius is smaller by 4 micrometers. We link these in-situ measurements of cloud modification by aerosols, for the first time, with collocated satellite broadband radiative flux observations from the Clouds and the Earth s Radiant Energy System to show that these microphysical effects of aerosols enhance the top-of-atmosphere cooling by -.9.9 plus or minus 4.3 W m(sup -2) for overcast conditions.

  11. The Influence of Aerosols on the Shortwave Cloud Radiative Forcing from North Pacific Oceanic Clouds: Results from the Cloud Indirect Forcing Experiment (CIFEX)

    NASA Technical Reports Server (NTRS)

    Wilcox, Eric M.; Roberts, Greg; Ramanathan, V.

    2006-01-01

    Aerosols over the Northeastern Pacific Ocean enhance the cloud drop number concentration and reduce the drop size for marine stratocumulus and cumulus clouds. These microphysical effects result in brighter clouds, as evidenced by a combination of aircraft and satellite observations. In-situ measurements from the Cloud Indirect Forcing Experiment (CIFEX) indicate that the mean cloud drop number concentration in low clouds over the polluted marine boundary layer is greater by 53/cu cm compared to clean clouds, and the mean cloud drop effective radius is smaller by 4 microns. We link these in-situ measurements of cloud modification by aerosols, for the first time, with collocated satellite broadband radiative flux observations from the Clouds and the Earth's Radiant Energy System (CERES) to show that these microphysical effects of aerosols enhance the top-of-atmosphere cooling by -9.9+/-4.3 W/sq m for overcast conditions.

  12. Column-integrated aerosol optical properties from ground-based spectroradiometer measurements at Barrax (Spain) during the Digital Airborne Imaging Spectrometer Experiment (DAISEX) campaigns

    NASA Astrophysics Data System (ADS)

    Pedrós, Roberto; Martinez-Lozano, Jose A.; Utrillas, Maria P.; Gómez-Amo, José L.; Tena, Fernando

    2003-09-01

    The Digital Airborne Imaging Spectrometer Experiment (DAISEX) was carried out for the European Space Agency (ESA) in order to develop the potential of spaceborne imaging spectroscopy for a range of different scientific applications. DAISEX involved simultaneous data acquisitions using different airborne imaging spectrometers over test sites in southeast Spain (Barrax) and the Upper Rhine valley (Colmar, France, and Hartheim, Germany). This paper presents the results corresponding to the column-integrated aerosol optical properties from ground-based spectroradiometer measurements over the Barrax area during the DAISEX campaign days in the years 1998, 1999, and 2000. The instruments used for spectral irradiance measurements were two Licor 1800 and one Optronic OL-754 spectroradiometers. The analysis of the spectral aerosol optical depth in the visible range shows in all cases the predominance of the coarse-particle mode over the fine-particle mode. The analysis of the back trajectories of the air masses indicates a predominance of marine-type aerosols in the lower atmospheric layers in all cases. Overall, the results obtained show that during the DAISEX there was a combination of maritime aerosols with smaller continental aerosols.

  13. Type-segregated aerosol effects on regional monsoon activity: A study using ground-based experiments and model simulations

    NASA Astrophysics Data System (ADS)

    Vijayakumar, K.; Devara, P. C. S.; Sonbawne, S. M.

    2014-12-01

    Classification of observed aerosols into key types [e.g., clean-maritime (CM), desert-dust (DD), urban-industrial/biomass-burning (UI/BB), black carbon (BC), organic carbon (OC) and mixed-type aerosols (MA)] would facilitate to infer aerosol sources, effects, and feedback mechanisms, not only to improve the accuracy of satellite retrievals but also to quantify the assessment of aerosol radiative impacts on climate. In this paper, we report the results of a study conducted in this direction, employing a Cimel Sun-sky radiometer at the Indian Institute of Tropical Meteorology (IITM), Pune, India during 2008 and 2009, which represent two successive contrasting monsoon years. The study provided an observational evidence to show that the local sources are subject to heavy loading of absorbing aerosols (dust and black carbon), with strong seasonality closely linked to the monsoon annual rainfall cycle over Pune, a tropical urban station in India. The results revealed the absence of CM aerosols in the pre-monsoon as well as in the monsoon seasons of 2009 as opposed to 2008. Higher loading of dust aerosols is observed in the pre-monsoon and monsoon seasons of 2009; majority may be coated with fine BC aerosols from local emissions, leading to reduction in regional rainfall. Further, significant decrease in coarse-mode AOD and presence of carbonaceous aerosols, affecting the aerosol-cloud interaction and monsoon-rain processes via microphysics and dynamics, is considered responsible for the reduction in rainfall during 2009. Additionally, we discuss how optical depth, contributed by different types of aerosols, influences the distribution of monsoon rainfall over an urban region using the Monitoring Atmospheric Composition and Climate (MACC) aerosol reanalysis. Furthermore, predictions of the Dust REgional Atmospheric Model (DREAM) simulations combined with HYSPLIT (HYbrid Single Particle Lagrangian Integrated Trajectory) cluster model are also discussed in support of the

  14. Experiments to investigate direct containment heating phenomena with scaled models of the Surry Nuclear Power Plant

    SciTech Connect

    Blanchat, T.K.; Allen, M.D.; Pilch, M.M.; Nichols, R.T.

    1994-06-01

    The Containment Technology Test Facility (CTTF) and the Surtsey Test Facility at Sandia National Laboratories are used to perform scaled experiments that simulate High Pressure Melt Ejection accidents in a nuclear power plant (NPP). These experiments are designed to investigate the effects of direct containment heating (DCH) phenomena on the containment load. High-temperature, chemically reactive melt (thermite) is ejected by high-pressure steam into a scale model of a reactor cavity. Debris is entrained by the steam blowdown into a containment model where specific phenomena, such as the effect of subcompartment structures, prototypic air/steam/hydrogen atmospheres, and hydrogen generation and combustion, can be studied. Four Integral Effects Tests (IETs) have been performed with scale models of the Surry NPP to investigate DCH phenomena. The 1/61{sup th} scale Integral Effects Tests (IET-9, IET-10, and IET-11) were conducted in CTRF, which is a 1/6{sup th} scale model of the Surry reactor containment building (RCB). The 1/10{sup th} scale IET test (IET-12) was performed in the Surtsey vessel, which had been configured as a 1/10{sup th} scale Surry RCB. Scale models were constructed in each of the facilities of the Surry structures, including the reactor pressure vessel, reactor support skirt, control rod drive missile shield, biological shield wall, cavity, instrument tunnel, residual heat removal platform and heat exchangers, seal table room and seal table, operating deck, and crane wall. This report describes these experiments and gives the results.

  15. Drop-tower experiments for capillary surfaces in an exotic container

    NASA Technical Reports Server (NTRS)

    Concus, Paul; Finn, Robert; Weislogel, Mark

    1991-01-01

    Low-gravity drop-tower experiments are carried out for an 'exotic' rotationally-symmetric container, which admits an entire continuum of distinct equilibrium symmetric capillary free surfaces. It is found that an initial equilibrium planer interface, a member of the continuum, will reorient toward a non-symmetric interface, as predicted by recent mathematical theory.

  16. Drop-tower experiments for capillary surfaces in an exotic container

    SciTech Connect

    Concus, P. ); Finn, R. . Dept. of Mathematics); Weislogel, M. . Lewis Research Center)

    1990-10-01

    Low-gravity drop-tower experiments are carried out for an exotic'' rotationally-symmetric container, which admits an entire continuum of distinct equilibrium symmetric capillary free surfaces. It is found that an initial equilibrium planar interface, a member of the continuum, will reorient toward a non-symmetric interface, as predicted by recent mathematical theory. 7 refs., 4 figs.

  17. Radiative Effects of Aerosols

    NASA Technical Reports Server (NTRS)

    Valero, Francisco P. J.

    1997-01-01

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

  18. Size distribution, composition and origin of the submicron aerosol in the marine boundary layer during the eastern Mediterranean "SUB-AERO" experiment

    NASA Astrophysics Data System (ADS)

    Eleftheriadis, K.; Colbeck, I.; Housiadas, C.; Lazaridis, M.; Mihalopoulos, N.; Mitsakou, C.; Smolík, J.; Ždímal, V.

    A period of intensive physical and chemical aerosol characterisation measurements was held over 5 days during July 2000 as part of the European SUB-AERO experiment.. Concurrent measurements were performed at the Finokalia remote coastal site on the island of Crete (Greece) and onboard the R/V " Aegaeon" which cruised in south part of the Aegean Sea northwards of Crete. The objective of the study was to investigate the spatial and temporal variability of microphysical parameters of the submicron aerosol and their dependence on airmass origin and chemical composition. The results reflect the submicron aerosol properties during airmass transport from the north including Europe and the Balkans and are in line with other studies on the aerosol properties of polluted continental air entering the marine boundary layer (MBL). Concentrations of submicron particulate matter (PM) mass were relatively higher at sea (20 μg m -3) compared to the coastal site (16 μg m -3). Concentrations of both organic carbon and sulphate, being the major water soluble component, were also higher at sea than at land. The high concentrations of ammonium and those of the water soluble organics, such as oxalate, can be attributed to emissions from mainland forest fires. The submicron aerosol number size distribution was unimodal with mobility mean diameters ( dg) ranging from 98 to 144 μm and standard deviations ( σg) from 1.56 to 1.9. Aerosol number concentrations at Finokalia were at least 50% lower especially when R/V Aegaeon sampled polluted air, but the modal parameters of the size distribution were very similar ( dg: 111-120, σg: 1.55-1.91). The surface MBL, under these conditions, was an aerosol rich environment where aerosol particles were transported both by the surface wind, advected from higher layers, chemically processed by interactions with gaseous precursors and physically altered by water vapour. The number to volume ratio for the submicrometer aerosol fraction reflected the

  19. SAGE II aerosol data validation based on retrieved aerosol model size distribution from SAGE II aerosol measurements

    NASA Technical Reports Server (NTRS)

    Wang, Pi-Huan; Mccormick, M. P.; Mcmaster, L. R.; Chu, W. P.; Swissler, T. J.; Osborn, M. T.; Russell, P. B.; Oberbeck, V. R.; Livingston, J.; Rosen, J. M.

    1989-01-01

    Consideration is given to aerosol correlative measurements experiments for the Stratospheric Aerosol and Gas Experiment (SAGE) II, conducted between November 1984 and July 1986. The correlative measurements were taken with an impactor/laser probe, a dustsonde, and an airborne 36-cm lidar system. The primary aerosol quantities measured by the ground-based instruments are compared with those calculated from the aerosol size distributions from SAGE II aerosol extinction measurements. Good agreement is found between the two sets of measurements.

  20. An Investigation of Aerosol Measurements from the Halogen Occultation Experiment: Validation, Size Distributions, Composition, and Relation to Other Chemical Species

    NASA Technical Reports Server (NTRS)

    Deshler, Terry; Hervig, Mark E.

    1998-01-01

    The efforts envisioned within the original proposal (accepted February 1994) and the extension of this proposal (accepted February 1997) included measurement validations, the retrieval of aerosol size distributions and distribution moments, aerosol correction studies, and investigations of polar stratospheric clouds. A majority of the results from this grant have been published. The principal results from this grant are discussed.

  1. Interpretation of FRESCO cloud retrievals in case of absorbing aerosol events

    NASA Astrophysics Data System (ADS)

    Wang, P.; Tuinder, O. N. E.; Tilstra, L. G.; Stammes, P.

    2011-12-01

    Cloud and aerosol information is needed in trace gas retrievals from satellite measurements. The Fast REtrieval Scheme for Clouds from the Oxygen A band (FRESCO) cloud algorithm employs reflectance spectra of the O2 A band around 760 nm to derive cloud pressure and effective cloud fraction. In general, clouds contribute more to the O2 A band reflectance than aerosols. Therefore, the FRESCO algorithm does not correct for aerosol effects in the retrievals and attributes the retrieved cloud information entirely to the presence of clouds, and not to aerosols. For events with high aerosol loading, aerosols may have a dominant effect, especially for almost cloud-free scenes. We have analysed FRESCO cloud data and Absorbing Aerosol Index (AAI) data from the Global Ozone Monitoring Experiment (GOME-2) instrument on the Metop-A satellite for events with typical absorbing aerosol types, such as volcanic ash, desert dust and smoke. We find that the FRESCO effective cloud fractions are correlated with the AAI data for these absorbing aerosol events and that the FRESCO cloud pressures contain information on aerosol layer pressure. For cloud-free scenes, the derived FRESCO cloud pressures are close to those of the aerosol layer for optically thick aerosols. For cloudy scenes, if the strongly absorbing aerosols are located above the clouds, then the retrieved FRESCO cloud pressures may represent the height of the aerosol layer rather than the height of the clouds. Combining FRESCO cloud data and AAI, an estimate for the aerosol layer pressure can be given, which can be beneficial for aviation safety and operations in case of e.g. volcanic ash plumes.

  2. Characterization of PM2.5 aerosols dominated by local pollution and Asian dust observed at an urban site in Korea during aerosol characterization experiments (ACE)--Asia Project.

    PubMed

    Park, Seung Shik; Kim, Young J; Cho, Sung Yong; Kim, Seung Jai

    2007-04-01

    Daily fine particulate matter (PM2.5) samples were collected at Gwangju, Korea, during the Aerosol Characterization Experiments (ACE)-Asia Project to determine the chemical properties of PM2.5 originating from local pollution and Asian dust (AD) storms. During the study period, two significant events occurred on April 10-13 and 24-25, 2001, and a minor event occurred on April 19, 2001. Based on air mass transport pathways identified by back-trajectory calculation, the PM2.5 dataset was classified into three types of aerosol populations: local pollution and two AD aerosol types. The two AD types were transported along different pathways. One originated from Gobi desert area in Mongolia, passing through Hunshandake desert in Northern Inner Mongolia, urban and polluted regions of China (AD1), and the other originated in sandy deserts located in the Northeast Inner Mongolia Plateau and then flowed southward through the Korean peninsula (AD2). During the AD2 event, a smoke plume that originated in North Korea was transported to our study site. Mass balance closures show that crustal materials were the most significant species during both AD events, contributing -48% to the PM2.5 mass; sulfate aerosols (19.1%) and organic matter (OM; 24.6%) were the second greatest contributors during the AD1 and AD2 periods, respectively, indicating that aerosol properties were dependent on the transport pathway. The sulfate concentration constituted only 6.4% (4.5 microg/m3) of the AD2 PM2.5 mass. OM was the major chemical species in the local pollution-dominated PM2.5 aerosols, accounting for 28.7% of the measured PM2.5 mass, followed by sulfate (21.4%), nitrate (15%), ammonium (12.8%), elemental carbon (8.9%), and crustal material (6.5%). Together with substantial enhancement of the crustal elements (Mg, Al, K, Ca, Sc, Ti, Mn, Fe, Sr, Zr, Ba, and Ce), higher concentrations of pollution elements (S, V, Ni, Zn, As, Cd, and Pb) were observed during AD1 and AD2 than during the local

  3. Physical and Chemical Properties of Anthropogenic Aerosols: An Overview

    EPA Science Inventory

    Aerosol chemical composition is complex. Combustion aerosols can comprise tens of thousands of organic compounds, refractory brown and black carbon, heavy metals, cations, anions, salts, and other inorganic phases. Aerosol organic matter normally contains semivolatile material th...

  4. Systemic immune cell response in rats after pulmonary exposure to manganese-containing particles collected from welding aerosols.

    PubMed

    Antonini, James M; Zeidler-Erdely, Patti C; Young, Shih-Houng; Roberts, Jenny R; Erdely, Aaron

    2012-01-01

    Welding fume inhalation affects the immune system of exposed workers. Manganese (Mn) in welding fume may induce immunosuppressive effects. The goal was to determine if Mn in welding fume alters immunity by reducing the number of circulating total leukocytes and specific leukocyte sub-populations. Sprague-Dawley rats were treated by intratracheal instillation (ITI) with either a single dose (2.00 mg/rat) or repeated doses (0.125 or 2.00 mg/rat for 7 weeks) with welding fumes that contained different levels of Mn. Additional rats were treated by ITI once a week for 7 weeks with the two doses of manganese chloride (MnCl₂). Bronchoalveolar lavage was performed to assess lung inflammation. Also, whole blood was recovered, and the number of circulating total leukocytes, as well as specific lymphocyte subsets, was determined by flow cytometry. The welding fume highest in Mn content significantly increased lung inflammation, injury, and production of inflammatory cytokines and chemokines compared to all other treatment groups. In addition, the same group expressed significant decreases in the number of circulating CD4⁺ and CD8⁺ T-lymphocytes after a single exposure, and significant reductions in the number of circulating total lymphocytes, primarily CD4⁺ and CD8⁺ T-lymphocytes, after repeated exposures (compared to control values). Repeated MnCl₂ exposure led to a trend of a reduction (but not statistically significant) in circulating total lymphocytes, attributable to the changes in the CD4⁺ T-lymphocyte population levels. The welding fume with the lower concentration of Mn had no significant effect on the numbers of blood lymphocytes and lymphocyte subsets compared to control values. Evidence from this study indicates that pulmonary exposure to certain welding fumes cause decrements in systemic immune cell populations, specifically circulating T-lymphocytes, and these alterations in immune cell number are not dependent exclusively on Mn, but likely a

  5. Sodium oxide and uranium oxide aerosol experiments: NSPP Tests 106-108 and Tests 204-207, data record report

    SciTech Connect

    Adams, R.E.; Kress, T.S.; Tobias, M.L.

    1981-03-01

    This data record report describes three sodium oxide aerosol tests and four uranium oxide aerosol tests conducted in the Nuclear Safety Pilot Plant project at Oak Ridge National Laboratory. The goal of this project is to establish the validity (or level of conservatism) of the aerosol behavioral code, HAARM-3, and follow-on codes under development at the Battelle Columbus Laboratories for the US Nuclear Regulatory Commission. Descriptions of the seven tests with tables and graphs summarizing the results are included. 92 figs.

  6. Investigation of the relative fine and coarse mode aerosol loadings and properties in the Southern Arabian Gulf region

    NASA Astrophysics Data System (ADS)

    Kaku, Kathleen C.; Reid, Jeffrey S.; Reid, Elizabeth A.; Ross-Langerman, Kristy; Piketh, Stuart; Cliff, Steven; Al Mandoos, Abdulla; Broccardo, Stephen; Zhao, Yongjing; Zhang, Jianglong; Perry, Kevin D.

    2016-03-01

    The aerosol chemistry environment of the Arabian Gulf region is extraordinarily complex, with high concentrations of dust aerosols from surrounding deserts mixed with anthropogenic aerosols originating from a large petrochemical industry and pockets of highly urbanized areas. Despite the high levels of aerosols experienced by this region, little research has been done to explore the chemical composition of both the anthropogenic and mineral dust portion of the aerosol burden. The intensive portion of the United Arab Emirates Unified Aerosol Experiment (UAE2), conducted during August and September 2004 was designed in part to resolve the aerosol chemistry through the use of multiple size-segregated aerosol samplers. The coarse mode mass (derived by subtracting the PM2.5 aerosol mass from the PM10 mass) is largely dust at 76% ± 7% of the total coarse mode mass, but is significantly impacted by anthropogenic pollution, primarily sulfate and nitrate. The PM2.5 aerosol mass also contains a large dust burden, at 38% ± 26%, but the anthropogenic component dominates. The total aerosol burden has significant impact not only on the atmosphere, but also the local population, as the air quality levels for both the PM10 and PM2.5 aerosol masses reached unhealthy levels for 24% of the days sampled.

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

    NASA Astrophysics Data System (ADS)

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

    2015-04-01

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

  8. The first experience the transportation of deep-water methane hydrates in a container

    NASA Astrophysics Data System (ADS)

    Egorov, A. V.; Rimskii-Korsakov, N. A.; Rozhkov, A. N.; Chernyaev, E. S.

    2011-04-01

    Deep-water experiments on the transportation of collected samples of methane hydrates from a lake's bottom to a support container were carried out as part of the MIRY na Baikale (2008-2009) expedition run by the Russian Academy of Sciences. High pressures and low temperatures are necessary for gas hydrates stability. As a sample of the hydrate is lifted to the water's surface, it intensively decomposes into water and methane gas. To reduce the decomposition, we used a container in which the hydrate's sample occurs in a gas medium rather than in water, which results in a substantial reduction in the rate of the heat exchange. At that, the gas for the container's filling was supplied by the hydrate itself due to its partial decomposition. To estimate the method's efficiency, we observed the hydrate's decomposition during lifting from a depth of 1400 m using different transportation techniques such as gas- or water-filled containers or fixing the sample in the manipulator's arm of the submersible. The sample in the gaseous medium was the only one that was safely delivered on board the support container, while the two others completely decomposed during the transportation. It is remarkable that all the samples started to decompose simultaneously at a depth of 380 m but their decomposition occurred at different rates.

  9. NASA-Lewis in-pile high temperature reactor meltdown containment experiment

    NASA Astrophysics Data System (ADS)

    Rom, Frank E.; Finnegan, Patrick M.; Gumto, Klaus H.

    1995-01-01

    The purpose of the in-pile meltdown experiment was to demonstrate the feasibility of a proposed concept for preventing melt-through of the containment vessel during and after the meltdown of a nuclear reactor. The concept was modeled and tested in the NASA Plum Brook Reactor Facility using fission heating to simulate fission product heating. In the concept a 38 mm (1.5 in) thick depleted UO2 pellet liner was placed on the inner surface of the stainless steel containment vessel. The high density, high melting point, and poor thermal conductivity of the UO2 pellet liner prevents molten materials from reaching the containment vessel walls. In turn, this results in a substantial increase in temperature of the molten pool. The high pool temperature causes the heat generating fission products to more quickly vaporize and condense throughout cooler regions within the containment volume. (At its melting point UO2 vaporizes at the rate of about 0.14 mm/s (0.006 in/s). Most fission products and their compounds vaporize even more rapidly.) The net effect is to reduce by orders of magnitude the heat flux through the containment vessel wall. A detailed physical description of the meltdown and containment process as derived from interpretation of the experimental measurements is presented. After meltdown, temperatures of the Mo-UO2 core exceeded 3393 K (5647 °F), which surpassed the melting point of UO2 by 503 K (905 °F) and Mo by 313 K (563 °F). Temperatures at the midpoint of the depleted UO2 liner never exceeded 1300 K (1934 °F). No molten material penetrated as much as halfway through the UO2 barrier. The peak surface temperature of the stainless steel containment vessel never exceeded 928 K (1210 °F).

  10. Stratospheric Aerosol and Gas Experiment, SAGE III on ISS, An Earth Science Mission on the International Space Station, Schedule Risk Analysis, A Project Perspective

    NASA Technical Reports Server (NTRS)

    Bonine, Lauren

    2015-01-01

    The presentation provides insight into the schedule risk analysis process used by the Stratospheric Aerosol and Gas Experiment III on the International Space Station Project. The presentation focuses on the schedule risk analysis process highlighting the methods for identification of risk inputs, the inclusion of generic risks identified outside the traditional continuous risk management process, and the development of tailored analysis products used to improve risk informed decision making.

  11. Intercomparison of stratospheric water vapor observed by satellite experiments: Stratospheric Aerosol and Gas Experiment II versus Limb Infrared Monitor of the Stratosphere and Atmospheric Trace Molecule Spectroscopy

    SciTech Connect

    Chiou, E.W.; Larsen, J.C. ); McCormick, M.P.; McMaster, L.R.; Chu, W.P. ); Rind, D. ); Oltmans, S. )

    1993-03-20

    This paper presents a comparison of the stratospheric water vapor measurements made by the satellite-borne sensors the Stratospheric Aerosol and Gas Experiment II (SAGE II), the Nimbus 7 Limb Infrared Monitor of the Stratosphere (LIMS), and the Spacelab 3 Atmospheric Trace Molecule Spectroscopy (ATMOS) experiment. LIMS obtained data for 7 months between November 1978 and May 1979; ATMOS was carried on Shuttle and observed eight profiles from April 30 to May 6, 1985 at approximately 30[degrees]N and 50[degrees]S; and, SAGE II continues to make measurements since its launch in October 1984. For both 30[degrees]N and 50[degrees]S in May, the comparisons between SAGE II and ATMOS show agreement within the estimated combined uncertainty of the two experiments. Several important features identified by LIMS observations have been confirmed by SAGE II: a well-developed hygropause in the lower stratosphere at low- to mid-latitudes, a poleward latitudinal gradient, increasing water vapor mixing ratios with altitude in the tropics, and the transport of dry lower stratospheric water vapor upward and southward in May, and upward and northward in November. A detailed comparative study also indicates that the two previously suggested corrections for LIMS, a correction in tropical lower stratosphere due to a positive temperature bias and the correction above 28 km based on improved emissivities will bring LIMS measurements much closer to those of SAGE II. The only significant difference occurs at high southern latitudes in May below 18 km, where LIMS measurements are 2-3 ppmv greater. It should be noted that LIMS observations are from 16 to 50 km, ATMOS from 14 to 86 km, and SAGE II from mid-troposphere to 40 km. With multiyear coverage, SAGE II observations should be useful for studying tropospheric-stratospheric exchange, for stratospheric transport, and for preparing water vapor climatologies for the stratosphere and the upper troposphere. 32 refs., 14 figs., 2 tabs.

  12. Uranium oxide and sodium oxide aerosol experiments: NSPP mixed-oxide tests 303-307, data record report. [LMFBR

    SciTech Connect

    Adams, R.E.; Kress, T.S.; Tobias, M.L.

    1982-10-01

    This data record report summarizes five tests, involving mixtures of uranium oxide and sodium oxide aerosols, conducted in the Nuclear Safety Pilot Plant project at Oak Ridge National Laboratory. The goal of this project is to establish the validity (or level of conservatism) of the aerosol behavioral code, HAARM-3, and follow-on codes under development at Battelle Columbus Laboratories for the US Nuclear Regulatory Commission. Descriptions of the five tests with tables and graphs summarizing the results are included.

  13. On the relationship between aerosol content and errors in telephotometer experiments.

    NASA Technical Reports Server (NTRS)

    Thomas, R. W. L.

    1971-01-01

    This paper presents an invariant imbedding theory of multiple scattering phenomena contributing to errors in telephotometer experiments. The theory indicates that there is a simple relationship between the magnitudes of the errors introduced by successive orders of scattering and it is shown that for all optical thicknesses each order can be represented by a coefficient which depends on the field of view of the telescope and the properties of the scattering medium. The verification of the theory and the derivation of the coefficients have been accomplished by a Monte Carlo program. Both monodisperse and polydisperse systems of Mie scatterers have been treated. The results demonstrate that for a given optical thickness the coefficients increase strongly with the mean particle size particularly for the smaller fields of view.

  14. Formation of highly porous aerosol particles by atmospheric freeze-drying in ice clouds.

    PubMed

    Adler, Gabriela; Koop, Thomas; Haspel, Carynelisa; Taraniuk, Ilya; Moise, Tamar; Koren, Ilan; Heiblum, Reuven H; Rudich, Yinon

    2013-12-17

    The cycling of atmospheric aerosols through clouds can change their chemical and physical properties and thus modify how aerosols affect cloud microphysics and, subsequently, precipitation and climate. Current knowledge about aerosol processing by clouds is rather limited to chemical reactions within water droplets in warm low-altitude clouds. However, in cold high-altitude cirrus clouds and anvils of high convective clouds in the tropics and midlatitudes, humidified aerosols freeze to form ice, which upon exposure to subsaturation conditions with respect to ice can sublimate, leaving behind residual modified aerosols. This freeze-drying process can occur in various types of clouds. Here we simulate an atmospheric freeze-drying cycle of aerosols in laboratory experiments using proxies for atmospheric aerosols. We find that aerosols that contain organic material that undergo such a process can form highly porous aerosol particles with a larger diameter and a lower density than the initial homogeneous aerosol. We attribute this morphology change to phase separation upon freezing followed by a glass transition of the organic material that can preserve a porous structure after ice sublimation. A porous structure may explain the previously observed enhancement in ice nucleation efficiency of glassy organic particles. We find that highly porous aerosol particles scatter solar light less efficiently than nonporous aerosol particles. Using a combination of satellite and radiosonde data, we show that highly porous aerosol formation can readily occur in highly convective clouds, which are widespread in the tropics and midlatitudes. These observations may have implications for subsequent cloud formation cycles and aerosol albedo near cloud edges. PMID:24297908

  15. Formation of highly porous aerosol particles by atmospheric freeze-drying in ice clouds

    PubMed Central

    Adler, Gabriela; Koop, Thomas; Haspel, Carynelisa; Taraniuk, Ilya; Moise, Tamar; Koren, Ilan; Heiblum, Reuven H.; Rudich, Yinon

    2013-01-01

    The cycling of atmospheric aerosols through clouds can change their chemical and physical properties and thus modify how aerosols affect cloud microphysics and, subsequently, precipitation and climate. Current knowledge about aerosol processing by clouds is rather limited to chemical reactions within water droplets in warm low-altitude clouds. However, in cold high-altitude cirrus clouds and anvils of high convective clouds in the tropics and midlatitudes, humidified aerosols freeze to form ice, which upon exposure to subsaturation conditions with respect to ice can sublimate, leaving behind residual modified aerosols. This freeze-drying process can occur in various types of clouds. Here we simulate an atmospheric freeze-drying cycle of aerosols in laboratory experiments using proxies for atmospheric aerosols. We find that aerosols that contain organic material that undergo such a process can form highly porous aerosol particles with a larger diameter and a lower density than the initial homogeneous aerosol. We attribute this morphology change to phase separation upon freezing followed by a glass transition of the organic material that can preserve a porous structure after ice sublimation. A porous structure may explain the previously observed enhancement in ice nucleation efficiency of glassy organic particles. We find that highly porous aerosol particles scatter solar light less efficiently than nonporous aerosol particles. Using a combination of satellite and radiosonde data, we show that highly porous aerosol formation can readily occur in highly convective clouds, which are widespread in the tropics and midlatitudes. These observations may have implications for subsequent cloud formation cycles and aerosol albedo near cloud edges. PMID:24297908

  16. In situ measurements of trace gases and aerosol optical properties at a rural site in northern China during East Asian Study of Tropospheric Aerosols: An International Regional Experiment 2005

    NASA Astrophysics Data System (ADS)

    Li, Can; Marufu, Lackson T.; Dickerson, Russell R.; Li, Zhanqing; Wen, Tianxue; Wang, Yuesi; Wang, Pucai; Chen, Hongbin; Stehr, Jeffrey W.

    2007-11-01

    In situ measurements of trace gases and aerosol optical properties were made in March 2005 at Xianghe (39.798°N, 116.958°E, 35 m), a rural site about 70 km southeast, and generally downwind of the Beijing metropolitan area. High pollutant levels were observed during the experiment, with CO (1.09 ± 1.02 ppmv, average ± standard deviation), SO2 (17.8 ± 15.7 ppbv), NOy (26.0 ± 24.0 ppbv), aerosol scattering coefficients (bsp, (468 ± 472) × 10-6 m-1), and aerosol absorption coefficients (bap, (65 ± 75) × 10-6 m-1) all much higher than observed at some rural sites in the United States. O3 (29.1 ± 16.5 ppbv) was relatively low during this study, suggesting inactive photochemical processes. Strong synoptic fluctuations in pollutant levels were detected every 4-5 days during the experiment, as cold fronts passing over the region drastically reduced the ground-level pollution. Very little precipitation was measured during the whole observational period, implying pollutant uplift and transport by rain-free cold fronts and dry convection. The single scattering albedo (SSA) observed (0.81 in the morning and 0.85 in the afternoon) indicates strongly absorbing aerosols near surface. The observed CO/SO2 ratio (35.8) is higher than inventory values, but closer to the updated CO inventory of Streets et al. (2006) than to Streets et al. (2003) or Wang et al. (2005). The observed CO/NOy ratio agrees better with inventories. Further analysis suggests that such comparisons may shed some light on the quality of emission inventories, but quantification of any error requires more extensive measurements over longer period and larger areas, as well as direct characterization of emission sources, especially mobile sources and small boilers. Using black carbon (BC)/CO ratio from the experiment, BC emissions from China are estimated at about 1300 Gg (109 g)/yr, but could be as high as 2600 Gg/yr.

  17. Impact of aftertreatment devices on primary emissions and secondary organic aerosol formation potential from in-use diesel vehicles: results from smog chamber experiments

    NASA Astrophysics Data System (ADS)

    Chirico, R.; Decarlo, P. F.; Heringa, M. F.; Tritscher, T.; Richter, R.; Prevot, A. S. H.; Dommen, J.; Weingartner, E.; Wehrle, G.; Gysel, M.; Laborde, M.; Baltensperger, U.

    2010-06-01

    Diesel particulate matter (DPM) is a significant source of aerosol in urban areas and has been linked to adverse health effects. Although newer European directives have introduced increasingly stringent standards for primary PM emissions, gaseous organics emitted from diesel cars can still lead to large amounts of secondary organic aerosol (SOA) in the atmosphere. Here we present results from smog chamber investigations characterizing the primary organic aerosol (POA) and the corresponding SOA formation at atmospherically relevant concentrations for three in-use diesel vehicles with different exhaust aftertreatment systems. One vehicle lacked exhaust aftertreatment devices, one vehicle was equipped with a diesel oxidation catalyst (DOC) and the final vehicle used both a DOC and diesel particulate filter (DPF). The experiments presented here were obtained from the vehicles at conditions representative of idle mode, and for one car in addition at a speed of 60 km/h. An Aerodyne high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS) was used to measure the organic aerosol (OA) concentration and to obtain information on the chemical composition. For the conditions explored in this paper, primary aerosols from vehicles without a particulate filter consisted mainly of black carbon (BC) with a low fraction of organic matter (OM, OM/BC<0.5), while the subsequent aging by photooxidation resulted in a consistent production of SOA only for the vehicles without a DOC and with a deactivated DOC. After 5 h of aging ~80% of the total organic aerosol was on average secondary and the estimated "emission factor" for SOA was 0.23-0.56 g/kg fuel burned. In presence of both a DOC and a DPF, primary particles with a mobility diameter above 5 nm were 300±19 cm-3, and only 0.01 g SOA per kg fuel burned was produced within 5 h after lights on. The mass spectra indicate that POA was mostly a non-oxidized OA with an oxygen to carbon atomic ratio (O/C) ranging from 0.097 to 0

  18. Impact of aftertreatment devices on primary emissions and secondary organic aerosol formation potential from in-use diesel vehicles: results from smog chamber experiments

    NASA Astrophysics Data System (ADS)

    Chirico, R.; Decarlo, P. F.; Heringa, M. F.; Tritscher, T.; Richter, R.; Prévôt, A. S. H.; Dommen, J.; Weingartner, E.; Wehrle, G.; Gysel, M.; Laborde, M.; Baltensperger, U.

    2010-12-01

    Diesel particulate matter (DPM) is a significant source of aerosol in urban areas and has been linked to adverse health effects. Although newer European directives have introduced increasingly stringent standards for primary PM emissions, gaseous organics emitted from diesel cars can still lead to large amounts of secondary organic aerosol (SOA) in the atmosphere. Here we present results from smog chamber investigations characterizing the primary organic aerosol (POA) and the corresponding SOA formation at atmospherically relevant concentrations for three in-use diesel vehicles with different exhaust aftertreatment systems. One vehicle lacked exhaust aftertreatment devices, one vehicle was equipped with a diesel oxidation catalyst (DOC) and the third vehicle used both a DOC and diesel particulate filter (DPF). The experiments presented here were obtained from the vehicles at conditions representative of idle mode, and for one car in addition at a speed of 60 km/h. An Aerodyne high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS) was used to measure the organic aerosol (OA) concentration and to obtain information on the chemical composition. For the conditions explored in this paper, primary aerosols from vehicles without a particulate filter consisted mainly of black carbon (BC) with a low fraction of organic matter (OM, OM/BC < 0.5), while the subsequent aging by photooxidation resulted in a consistent production of SOA only for the vehicles without a DOC and with a deactivated DOC. After 5 h of aging ~80% of the total organic aerosol was on average secondary and the estimated "emission factor" for SOA was 0.23-0.56 g/kg fuel burned. In presence of both a DOC and a DPF, only 0.01 g SOA per kg fuel burned was produced within 5 h after lights on. The mass spectra indicate that POA was mostly a non-oxidized OA with an oxygen to carbon atomic ratio (O/C) ranging from 0.10 to 0.19. Five hours of oxidation led to a more oxidized OA with an O/C range of 0

  19. Smog chamber experiments to investigate Henry's law constants of glyoxal using different seed aerosols as well as imidazole formation in the presence of ammonia

    NASA Astrophysics Data System (ADS)

    Jakob, Ronit

    2015-04-01

    Aerosols play an important role in the chemistry and physics of the atmosphere. Hence, they have a direct as well as an indirect impact on the earth's climate. Depending on their formation, one distinguishes between primary and secondary aerosols[1]. Important groups within the secondary aerosols are the secondary organic aerosols (SOAs). In order to improve predictions about these impacts on the earth's climate the existing models need to be optimized, because they still underestimate SOA formation[2]. Glyoxal, the smallest α-dicarbonyl, not only acts as a tracer for SOA formation but also as a direct contributor to SOA. Because glyoxal has such a high vapour pressure, it was common knowledge that it does not take part in gas-particle partitioning and therefore has no impact on direct SOA formation. However, the Henry's law constant for glyoxal is surprisingly high. This has been explained by the hydration of the aldehyde groups, which means that a species with a lower vapour pressure is produced. Therefore the distribution of glyoxal between gas- and particle phase is atmospherically relevant and the direct contribution of glyoxal to SOA can no longer be neglected[3]. Besides this particulate glyoxal is able to undergo heterogeneous chemistry with gaseous ammonia to form imidazoles. This plays an important role for regions with aerosols exhibiting alkaline pH values for example from lifestock or soil dust because imidazoles as nitrogen containing compounds change the optical properties of aerosols[4]. A high salt concentration present in chamber seed aerosols leads to an enhanced glyoxal uptake into the particle. This effect is called "salting-in". The salting effect depends on the composition of the seed aerosol as well as the soluble compound. For very polar compounds, like glyoxal, a "salting-in" is observed[3]. Glyoxal particle formation during a smog chamber campaign at Paul-Scherrer-Institut (PSI) in Switzerland was examined using different seed aerosols

  20. AEROSOL INDUSTRY SUCCESS IN REDUCING CFC PROPELLANT USAGE

    EPA Science Inventory

    Part I of this report discusses the U.S. aerosol industry's experience in converting from chlorofluorocarbon (CFC) propellants to alternative aerosol formulations. Detailed examples of non-CFC formulations are provided for 28 categories of aerosol products. ydrocarbon propellants...

  1. The Charged Aerosol Release Experiment (Care II) to Study Artificial Dusty Plasmas in the Upper Atmosphere

    NASA Astrophysics Data System (ADS)

    Bernhardt, P. A.; Siefring, C. L.; Gatling, G.; Briczinski, S. J., Jr.; Vierinen, J.; Bhatt, A.; Holzworth, R. H., II; McCarthy, M.; Gustavsson, B.; La Hoz, C.; Latteck, R.

    2015-12-01

    A sounding rocket launched from Andoya, Norway in September 2015 carried 37 rocket motors and a multi-instrument daughter payload into the ionosphere to study the generation of plasma wave electric fields and ionospheric density disturbances by the high-speed injection of dust particles. The primary purpose of the CARE II mission is to validate the dress-particle theory of enhanced incoherent scatter from a dusty plasma and to validate models of plasma instabilities driven by high-speed charged particles. The CARE II chemical payload produces 66 kg of micron-sized dust particles composed of aluminium oxide. In addition to the dust, simple molecular combustion products such as N2, H2, CO2, CO, H20 and NO will be injected into the bottomside of the F-layer. Charging of the dust and ion charge exchange with the molecules yields plasma particles moving at hypersonic velocities. Streaming instabilities and shear electric fields causes plasma turbulence that can be detected using ground radars and in situ plasma instruments. The instrument payload was separated from the chemical release payload soon after launch to measure electric field vectors, electron and ion densities, and integrated electron densities from the rocket to the ground. The chemical release of high speed dust was directed upward on the downleg of the rocket trajectory to intersect the F-Layer. The instrument section was about 600 meters from the dust injection module at the release time. Ground HF and UHF radars were operated to detected scatter and refraction by the modified ionosphere. Optical instruments from airborne and ground observatories were used to map the dispersal of the dust using scattered sunlight. The plasma interactions are being simulated with both fluid and particle-in-cell (PIC) codes. CARE II is a follow-on to the CARE I rocket experiment conducted from Wallops Island Virginia in September 2009.

  2. Occupational exposure to inhalable and total aerosol in the primary nickel production industry.

    PubMed Central

    Tsai, P J; Vincent, J H; Wahl, G; Maldonado, G

    1995-01-01

    OBJECTIVES--This paper describes a study that was carried out in the primary nickel production industry to investigate the levels of personal exposure to aerosols containing nickel and the impact on exposure assessment of introducing new personal sampling techniques with performance consistent with the latest particle size-selective criteria. METHODS--Experiments were carried out at workplaces in mining, milling, smelting, and refining works to investigate the effect of changing from the current method of total aerosol (with the widely used 37 mm filter holder) to the new method of measuring inhalable aerosol (with the Institute of Occupational Medicine (IOM) inhalable aerosol sampler). RESULTS--The results show that inhalable aerosol exposure concentrations--for both overall aerosol and for total nickel--were consistently and significantly higher than the corresponding total aerosol concentrations. Weighted least squares linear regression yielded IOM/37 mm factors ranging from about 1.2 to 4.0. The exposure data for each company process were found to be log-normally distributed. CONCLUSIONS--The results suggest the possibility of generating a single pragmatic factor for each company process for converting current total aerosol exposures to new exposures based on the inhalability concept contained in the latest particle size-selective criteria for aerosol exposure assessment. Such data may be important in determining new occupational exposure limits for nickel. PMID:8563841

  3. Airborne measurements of black carbon aerosol over the Southeastern U.S. during the Southeast Atmosphere Study (SAS) experiment

    NASA Astrophysics Data System (ADS)

    Markovic, M. Z.; Perring, A. E.; Schwarz, J. P.; Fahey, D. W.; Gao, R.; Watts, L.; Holloway, J.; Graus, M.; Warneke, C.; De Gouw, J. A.; Veres, P. R.; Roberts, J. M.; Middlebrook, A. M.; Welti, A.; Liao, J.

    2013-12-01

    The Southeast Atmosphere Study (SAS) field campaign was a large-scale, collaborative project, which took place in the Southeastern U.S. in June and July of 2013. The goal of the campaign was to investigate the impacts of biogenic and anthropogenic gases and aerosols on the formation of haze and anomalous climate cooling in the region. During SAS, a NOAA Single Particle Soot Photometer (SP2) instrument was utilized onboard NOAA WP-3D research aircraft for measurements of black carbon (BC) aerosol mass and microphysical properties. BC aerosol is emitted into the atmosphere from biomass burning (BB) and incomplete combustion of fossil and biofuel. Hence, BC sources are strongly linked to anthropogenic activity. BC aerosol is currently the second largest anthropogenic climate forcing agent after CO2(g), and its climate impacts, which depend on vertical burden and internal mixing, are not fully understood. In the Southeast, BC aerosol is expected to provide surface area for the condensation of semi-volatile products of VOC oxidation and subsequent formation of secondary organic aerosol (SOA). Hence, BC is expected to impact the haze formation and regional climate. In this work we present an overview of BC measurements during Southeast Nexus (SENEX) study, the NOAA contribution to SAS. Geographical variations in mass mixing ratios, mass size distributions, and mixing state of BC over the Southeast U.S. are discussed. Relationships of BC with carbon monoxide (CO), acetonitrile (ACN) and other trace gases are used to investigate the impacts of urban, BB, natural gas development, and power plant emissions on the distribution and properties of BC aerosol in the region. Among studied urban centers, St. Louis and Atlanta were determined to be the largest source regions of BC. A clear weekend effect in BC mass mixing ratios and microphysical properties was observed in the metropolitan Atlanta region. Compared to BB and urban centers, power plants and natural gas developments

  4. A fine fraction of soil used as an aerosol analogue during the DUNE experiment: sequential solubility in water, decreasing pH step-by-step

    NASA Astrophysics Data System (ADS)

    Aghnatios, C.; Losno, R.; Dulac, F.

    2014-09-01

    A soil sample collected in a desert aerosol source area near Douz (southern Tunisia) was dry-sieved at 20 μm in order to extract the fraction similar to a wind-generated aerosol, and was used to seed mesocosms during the DUNE experiment (a DUst experiment in a low Nutrient, low chlorophyll Ecosystem). In this work, said "aerosol-like" fine dust was sequentially leached by short contacts with water at initial pHs, decreasing from seven to one, representing various wet environmental conditions. For each step, the solubility of a given element is calculated as the amount of its dissolved fraction, relative to its total amount. The evolution of this fractional solubility from the highest to lowest pHs provides information on the chemical strength needed to solubilise a given element and its lability. The behaviour of the elemental solubility was sorted into two groups: (1) Ca, Sr, Ba, Mn, and P, with a solubility between 23% and 70%, and a maximum sequential solubility at pH 3; (2) Al and Fe, with a solubility of less than 2% and the highest release at pH 1. Similar solubility patterns in group 1 for Ca, P, and Mn suggest a possible association of the elements in the same minerals, most probably carbonates.

  5. LMFBR aerosol release and transport program. Quarterly progress report, July-September 1981

    SciTech Connect

    Kress, T.S.; Tobias, M.L.

    1982-01-01

    This report summarizes progress for the Aerosol Release and Transport Program sponsored by the Office of Nuclear Regulatory Research, Division of Accident Evaluation of the Nuclear Regulatory Commission for the period July-September 1981. Topics discussed include (1) preparations for under-sodium tests at the Fast Aerosol Simulant Test Facility, (2) progress in interpretation of Oak Ridge National Laboratory-Sandia Laboratory normalization test results, (3) U/sub 3/O/sub 8/ in steam (light-water reactor accident) aerosol experiments conducted in the Nuclear Safety Power Plant, (4) experiments on B/sub 2/O/sub 3/ and SiO/sub 2/ aerosols at the Containment Research Installation-II Facility, (5) fuel-melting tests in small-scale experimental facilities for the core-melt aerosol program, (6) analytical comparison of simple adiabatic nonlinear and linear analytical models of bubble oscillation phenomena with experimental data.

  6. High temperature experiments on a 4 tons UF6 container TENERIFE program

    SciTech Connect

    Casselman, C.; Duret, B.; Seiler, J.M.; Ringot, C.; Warniez, P.

    1991-12-31

    The paper presents an experimental program (called TENERIFE) whose aim is to investigate the behaviour of a cylinder containing UF{sub 6} when exposed to a high temperature fire for model validation. Taking into account the experiments performed in the past, the modelization needs further information in order to be able to predict the behaviour of a real size cylinder when engulfed in a 800{degrees}C fire, as specified in the regulation. The main unknowns are related to (1) the UF{sub 6} behaviour beyond the critical point, (2) the relationship between temperature field and internal pressure and (3) the equivalent conductivity of the solid UF{sub 6}. In order to investigate these phenomena in a representative way it is foreseen to perform experiments with a cylinder of real diameter, but reduced length, containing 4 tons of UF{sub 6}. This cylinder will be placed in an electrically heated furnace. A confinement vessel prevents any dispersion of UF{sub 6}. The heat flux delivered by the furnace will be calibrated by specific tests. The cylinder will be changed for each test.

  7. Organic aerosols

    SciTech Connect

    Penner, J.E.

    1994-01-01

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

  8. Containment system for experiments on radioactive and other hazardous materials in a Paris-Edinburgh press

    DOE PAGESBeta

    Jacobsen, M. K.; Velisavljevic, N.

    2015-11-01

    Recent technical developments using the large volume Paris-Edinburgh press platform have enabled x-ray synchrotron studies at high pressure and temperature conditions. However, its application to some materials of interest, such as high hazard materials that require special handling due to safety issues, reactivity, or other challenges, has not been feasible without the introduction of special containment systems to eliminate the hazards. However, introduction of a containment system is challenging due to the requirement to provide full safety containment for operation in the variety of environments available, while not hindering any of the experimental probes that are available for inert samplemore » measurement. In this work, we report on the development and implementation of a full safety enclosure for a Paris-Edinburgh type press. During the initial development and subsequent application stage of work, experiments were performed on both cerium dioxide (CeO2) and uranium (U). As a result, this device allows for full implementation of all currently available experimental probes involving the Paris-Edinburgh press at the High Pressure Collaborative Access Team sector of the Advanced Photon Source.« less

  9. Containment system for experiments on radioactive and other hazardous materials in a Paris-Edinburgh press

    SciTech Connect

    Jacobsen, M. K. Velisavljevic, N.

    2015-11-15

    Recent technical developments using the large volume Paris-Edinburgh press platform have enabled x-ray synchrotron studies at high pressure and temperature conditions. However, its application to some materials of interest, such as high hazard materials that require special handling due to safety issues, reactivity, or other challenges, has not been feasible without the introduction of special containment systems to eliminate the hazards. However, introduction of a containment system is challenging due to the requirement to provide full safety containment for operation in the variety of environments available, while not hindering any of the experimental probes that are available for inert sample measurement. In this work, we report on the development and implementation of a full safety enclosure for a Paris-Edinburgh type press. During the initial development and subsequent application stage of work, experiments were performed on both cerium dioxide (CeO{sub 2}) and uranium (U). This device allows for full implementation of all currently available experimental probes involving the Paris-Edinburgh press at the High Pressure Collaborative Access Team sector of the Advanced Photon Source.

  10. Containment system for experiments on radioactive and other hazardous materials in a Paris-Edinburgh press

    NASA Astrophysics Data System (ADS)

    Jacobsen, M. K.; Velisavljevic, N.

    2015-11-01

    Recent technical developments using the large volume Paris-Edinburgh press platform have enabled x-ray synchrotron studies at high pressure and temperature conditions. However, its application to some materials of interest, such as high hazard materials that require special handling due to safety issues, reactivity, or other challenges, has not been feasible without the introduction of special containment systems to eliminate the hazards. However, introduction of a containment system is challenging due to the requirement to provide full safety containment for operation in the variety of environments available, while not hindering any of the experimental probes that are available for inert sample measurement. In this work, we report on the development and implementation of a full safety enclosure for a Paris-Edinburgh type press. During the initial development and subsequent application stage of work, experiments were performed on both cerium dioxide (CeO2) and uranium (U). This device allows for full implementation of all currently available experimental probes involving the Paris-Edinburgh press at the High Pressure Collaborative Access Team sector of the Advanced Photon Source.

  11. Containment system for experiments on radioactive and other hazardous materials in a Paris-Edinburgh press.

    PubMed

    Jacobsen, M K; Velisavljevic, N

    2015-11-01

    Recent technical developments using the large volume Paris-Edinburgh press platform have enabled x-ray synchrotron studies at high pressure and temperature conditions. However, its application to some materials of interest, such as high hazard materials that require special handling due to safety issues, reactivity, or other challenges, has not been feasible without the introduction of special containment systems to eliminate the hazards. However, introduction of a containment system is challenging due to the requirement to provide full safety containment for operation in the variety of environments available, while not hindering any of the experimental probes that are available for inert sample measurement. In this work, we report on the development and implementation of a full safety enclosure for a Paris-Edinburgh type press. During the initial development and subsequent application stage of work, experiments were performed on both cerium dioxide (CeO2) and uranium (U). This device allows for full implementation of all currently available experimental probes involving the Paris-Edinburgh press at the High Pressure Collaborative Access Team sector of the Advanced Photon Source. PMID:26628148

  12. Containment system for experiments on radioactive and other hazardous materials in a Paris-Edinburgh press

    SciTech Connect

    Jacobsen, M. K.; Velisavljevic, N.

    2015-11-20

    Recent technical developments using the large volume Paris-Edinburgh press platform have enabled x-ray synchrotron studies at high pressure and temperature conditions. However, its application to some materials of interest, such as high hazard materials that require special handling due to safety issues, reactivity, or other challenges, has not been feasible without the introduction of special containment systems to eliminate the hazards. However, introduction of a containment system is challenging due to the requirement to provide full safety containment for operation in the variety of environments available, while not hindering any of the experimental probes that are available for inert sample measurement. In this work, we report on the development and implementation of a full safety enclosure for a Paris-Edinburgh type press. During the initial development and subsequent application stage of work, experiments were performed on both cerium dioxide (CeO2) and uranium (U). As a result, this device allows for full implementation of all currently available experimental probes involving the Paris-Edinburgh press at the High Pressure Collaborative Access Team sector of the Advanced Photon Source.

  13. The nylon scintillator containment vessels for the Borexino solar neutrino experiment

    NASA Astrophysics Data System (ADS)

    Cadonati, L.; Calaprice, F.; Galbiati, C.; Pocar, A.; Shutt, T.

    2014-06-01

    The neutrino event rate in the Borexino scintillator is very low ( 0.5 events per day per ton) and concentrated in an energy region well below the 2.6 MeV threshold of natural radioactivity. The intrinsic radioactive contaminants in the photomultipliers (PMTs), in the Stainless Steel Sphere, and in other detector components, play special requirements on the system required to contain the scintillator. The liquid scintillator must be shielded from the Stainless Steel Sphere and from the PMTs by a thick barrier of buffer fluid. The fluid barrier, in addition, needs to be segmented in order to contain migration of radon and daughters emanated by the Stainless Steel Sphere and by the PMTs. These requirements were met by designing and building two spherical vessel made of thin nylon film. The inner vessel contains the scintillator, separating it from the surrounding buffer. The buffer region itself is divided into two concentric shells by the second, outer nylon vessel. In addition, the two nylon vessels must satisfy stringent requirements for radioactivity and for mechanical, optical and chemical properties. This paper describes the requirements of the the nylon vessels for the Borexino experiment and offers a brief overview of the construction methods adopted to meet those requirements.

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

    SciTech Connect

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

    2011-02-01

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

  15. Impacts of 20th century aerosol emissions on the South Asian monsoon in the CMIP5 models

    NASA Astrophysics Data System (ADS)

    Guo, L.; Turner, A. G.; Highwood, E. J.

    2014-12-01

    Comparison of single-forcing varieties of 20th century historical experiments in a subset of models from the Fifth Coupled Model Intercomparison Project (CMIP5) reveals that South Asian summer monsoon rainfall increases towards the present day in Greenhouse Gas (GHG)-only experiments with respect to pre-industrial levels, while it decreases in anthropogenic aerosol-only experiments. Comparison of these single-forcing experiments with the all-forcings historical experiment suggests aerosol emissions have dominated South Asian monsoon rainfall trends in recent decades, especially during the 1950s to 1970s. The variations in South Asian monsoon rainfall in these experiments follows approximately the time-evolution of inter-hemispheric temperature gradient over the same period, suggesting a contribution from the large-scale background state relating to the asymmetric distribution of aerosol emissions about the equator. By examining the twenty-five available all-forcings historical experiments, we show that models including aerosol indirect effects dominate the negative rainfall trend. Indeed, models including only the direct radiative effect of aerosol show an increase in monsoon rainfall, consistent with the dominance of increasing greenhouse gas emissions and planetary warming on monsoon rainfall in those models. For South Asia, reduced rainfall in the models with indirect effects is related to decreased evaporation at the land surface rather than from anomalies in horizontal moisture flux, suggesting the impact of indirect effects on local aerosol emissions. This is confirmed by examination of aerosol loading and cloud droplet number trends over the South Asia region. Thus while remote aerosols and their asymmetric distribution about the equator play a role in setting the inter-hemispheric temperature distribution on which the South Asian monsoon, as one of the global monsoons, operates, the addition of indirect aerosol effects acting on very local aerosol emissions

  16. Impacts of 20th century aerosol emissions on the South Asian monsoon in the CMIP5 models

    NASA Astrophysics Data System (ADS)

    Guo, L.; Turner, A. G.; Highwood, E. J.

    2015-06-01

    Comparison of single-forcing varieties of 20th century historical experiments in a subset of models from the Fifth Coupled Model Intercomparison Project (CMIP5) reveals that South Asian summer monsoon rainfall increases towards the present day in Greenhouse Gas (GHG)-only experiments with respect to pre-industrial levels, while it decreases in anthropogenic aerosol-only experiments. Comparison of these single-forcing experiments with the all-forcings historical experiment suggests aerosol emissions have dominated South Asian monsoon rainfall trends in recent decades, especially during the 1950s to 1970s. The variations in South Asian monsoon rainfall in these experiments follows approximately the time evolution of inter-hemispheric temperature gradient over the same period, suggesting a contribution from the large-scale background state relating to the asymmetric distribution of aerosol emissions about the equator. By examining the 24 available all-forcings historical experiments, we show that models including aerosol indirect effects dominate the negative rainfall trend. Indeed, models including only the direct radiative effect of aerosol show an increase in monsoon rainfall, consistent with the dominance of increasing greenhouse gas emissions and planetary warming on monsoon rainfall in those models. For South Asia, reduced rainfall in the models with indirect effects is related to decreased evaporation at the land surface rather than from anomalies in horizontal moisture flux, suggesting the impact of indirect effects on local aerosol emissions. This is confirmed by examination of aerosol loading and cloud droplet number trends over the South Asia region. Thus, while remote aerosols and their asymmetric distribution about the equator play a role in setting the inter-hemispheric temperature distribution on which the South Asian monsoon, as one of the global monsoons, operates, the addition of indirect aerosol effects acting on very local aerosol emissions also

  17. Radiative Effects of Aerosols

    NASA Technical Reports Server (NTRS)

    Valero, Francisco P. J.

    1996-01-01

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

  18. MCNP analysis of PNL split-table critical experiments containing mixed-oxide fuels

    SciTech Connect

    Abdurrahman, N.M.; Yavuz, M.; Radulescu, G.

    1997-12-01

    Pacific Northwest Laboratory (PNL) Split-Table Critical experiments containing mixed-oxide (MOX) fuels for various core configurations are studied using MCNP4A with the ENDF/B-VI continuous-energy library. These experiments were performed to provide necessary technical information and experimental criticality data that would serve as benchmark data in support of the liquid-metal fast breeder reactor program. Because of the current interest in the utilization of weapons-grade plutonium in the form of MOX fuel in light water reactors, such experimental data are extremely important for checking the performance of the modem computational tools. The {sup 239}Pu content in plutonium of the PNL MOX fuels is {approximately}91 wt%, which is very close to that of the weapons-grade {sup 239}Pu. The MOX fuels used in these critical experiments consist of 30.0, 14.62, and 7.89 wt% Pu and N{sub H}/(N{sub Pu} + Nu) moderation ratios (MRs) of 47.4, 30.6, and 51.8, respectively.

  19. Airborne Sunphotometer Measurements of Aerosol Optical Depth and Columnar Water Vapor During the Puerto Rico Dust Experiment, and Comparison with Land, Aircraft, and Satellite Measurements

    NASA Technical Reports Server (NTRS)

    Livingston, John M.; Russell, Philip B.; Reid, Jeffrey; Redemann, Jens; Schmid, Beat; Allen, Duane A.; Torres, Omar; Levy, Robert C.; Remer, Lorraine A.; Holben, Brent N.; Hipskind, R. Stephen (Technical Monitor)

    2002-01-01

    Analyses of aerosol optical depth (AOD) and columnar water vapor (CWV) measurements obtained with the six-channel NASA Ames Airborne Tracking Sunphotometer (AATS-6) mounted on a twin-engine aircraft during the summer 2000 Puerto Rico Dust Experiment are presented. In general, aerosol extinction values calculated from AATS-6 AOD measurements acquired during aircraft profiles up to 5 km ASL reproduce the vertical structure measured by coincident aircraft in-situ measurements of total aerosol number and surface area concentration. Calculations show that the spectral dependence of AOD was small (mean Angstrom wavelength exponents of approximately 0.20) within three atmospheric layers defined as the total column beneath the top of each aircraft profile, the region beneath the trade wind inversion, and the region within the Saharan Air Layer (SAL) above the trade inversion. This spectral behavior is consistent with attenuation of incoming solar radiation by large dust particles or by dust plus sea salt. Values of CWV calculated from profile measurements by AATS-6 at 941.9 nm and from aircraft in-situ measurements by a chilled mirror dewpoint hygrometer agree to within approximately 4% (0.13 g/sq cm). AATS-6 AOD values measured on the ground at Roosevelt Roads Naval Air Station and during low altitude aircraft runs over the adjacent Cabras Island aerosol/radiation ground site agree to within 0.004 to 0.030 with coincident data obtained with an AERONET Sun/sky Cimel radiometer located at Cabras Island. For the same observation times, AERONET retrievals of CWV exceed AATS-6 values by a mean of 0.74 g/sq cm (approximately 21 %) for the 2.9-3.9 g/sq cm measured by AATS-6. Comparison of AATS-6 aerosol extinction values obtained during four aircraft ascents over Cabras Island with corresponding values calculated from coincident aerosol backscatter measurements by a ground-based micro-pulse lidar (MPL-Net) located at Cabras yields a similar vertical structure above the trade

  20. A~fine fraction of soil used as an aerosol analogue during the DUNE experiment: sequential solubility in water with step-by-step decreasing pH

    NASA Astrophysics Data System (ADS)

    Aghnatios, C.; Losno, R.; Dulac, F.

    2014-02-01

    A soil sample collected in a desert aerosol source area near Douz (South Tunisia) was sieved at 20 μm in order to extract the fraction similar to an aerosol generated by wind and used to seed mesocosms during the DUNE experiment. In the present work, this "aerosol-like" fine dust was sequentially leached by short contacts with water at pHs decreasing from 7 to 1. These pHs are representative of various environmental wet conditions, the lowest of which could be reached during cloud conditions. The evolution of the solubility from the highest to the lowest pHs provides information on the necessary strength for the solubilisation of a given element and its lability. The behaviour of the elemental fractional solubility is sorted into two groups: (i) Ca, Sr, Ba, Mn, P constitute group 1, with a solubility between 23% and 70% and with a maximum solubility at pH 3; (ii) whereas in group 2 (Al, Fe), the solubility is less than 2% with the highest release at pH 1. Similar solubility patterns in group 1 for Ca, P and Mn suggest a~possible association of the elements in the same minerals, most probably carbonates, which gives phosphorus an unexpected high lability.

  1. Final Report: Part 1. In-Place Filter Testing Instrument for Nuclear Material Containers. Part 2. Canister Filter Test Standards for Aerosol Capture Rates.

    SciTech Connect

    Brown, Austin Douglas; Runnels, Joel T.; Moore, Murray E.; Reeves, Kirk Patrick

    2014-11-02

    A portable instrument has been developed to assess the functionality of filter sand o-rings on nuclear material storage canisters, without requiring removal of the canister lid. Additionally, a set of fifteen filter standards were procured for verifying aerosol leakage and pressure drop measurements in the Los Alamos Filter Test System. The US Department of Energy uses several thousand canisters for storing nuclear material in different chemical and physical forms. Specialized filters are installed into canister lids to allow gases to escape, and to maintain an internal ambient pressure while containing radioactive contaminants. Diagnosing the condition of container filters and canister integrity is important to ensure worker and public safety and for determining the handling requirements of legacy apparatus. This report describes the In-Place-Filter-Tester, the Instrument Development Plan and the Instrument Operating Method that were developed at the Los Alamos National Laboratory to determine the “as found” condition of unopened storage canisters. The Instrument Operating Method provides instructions for future evaluations of as-found canisters packaged with nuclear material. Customized stainless steel canister interfaces were developed for pressure-port access and to apply a suction clamping force for the interface. These are compatible with selected Hagan-style and SAVY-4000 storage canisters that were purchased from NFT (Nuclear Filter Technology, Golden, CO). Two instruments were developed for this effort: an initial Los Alamos POC (Proof-of-Concept) unit and the final Los Alamos IPFT system. The Los Alamos POC was used to create the Instrument Development Plan: (1) to determine the air flow and pressure characteristics associated with canister filter clogging, and (2) to test simulated configurations that mimicked canister leakage paths. The canister leakage scenarios included quantifying: (A) air leakage due to foreign material (i.e. dust and hair

  2. Organic composition of PM 2.5 and size-segregated aerosols and their sources during the 2002 Bay Regional Atmospheric Chemistry Experiment (BRACE), Florida, USA

    NASA Astrophysics Data System (ADS)

    Tremblay, Raphaël T.; Riemer, Daniel D.; Zika, Rod G.

    PM 2.5 and size-segregated aerosols were collected in May 2002 as part of the Bay Regional Atmospheric Chemistry Experiment (BRACE), Florida, USA. Aerosol organic composition was used to estimate sources of a series of alkanes and polycyclic aromatic hydrocarbons (PAHs) using chemical indices, hierarchical cluster analysis (HCA) and a chemical mass balance receptor model (CMB). Aerosols were collected on quartz fiber filters (QFF) using a PM 2.5 high volume sampler and on aluminum foil discs using a Micro-Orifice Uniform Deposit Impactor (MOUDI, 50% aerodynamic cut diameters were 18, 10, 5.6, 3.2, 1.8, 1.0, 0.56, 0.315 and 0.171 μm). Target compounds included alkanes and PAHs and were solvent extracted using a mixture of dichloromethane, acetone and hexane, concentrated and then analyzed using a gas chromatograph/mass spectrometer (GC/MS). The target compounds in PM 2.5 were dominated by six sources during the study period: mobile sources (39±5%), coal burning (33±5%), biogenic primary emission (20±2%), oil combustion (5±2%), biomass burning (1.0±0.3%) and an unidentified source (3±2%). Results obtained from the chemical indices, HCA and CMB were in very good agreement with each other. PAH size distributions are presented for days dominated by a same source. Seventy-five percent and 50% of the PAH were found below 1.8 and 0.56 μm, respectively (monthly PAH geometric diameters averaged 0.43 μm). Coarse size PAHs were observed on 1 day (15 May) and were correlated with nitrate and sodium size distribution. It is hypothesized that the PAHs, sodium and nitrate were internally mixed and that the PAHs deposited onto a pre-existing marine aerosol. This transfer process has significant implications for PAH deposition and lifetime and warrants further study.

  3. The remarkable effect of FeSO4 seed aerosols on secondary organic aerosol formation from photooxidation of α-pinene/NOx and toluene/NOx

    NASA Astrophysics Data System (ADS)

    Chu, Biwu; Hao, Jiming; Takekawa, Hideto; Li, Junhua; Wang, Kun; Jiang, Jingkun

    2012-08-01

    To investigate the effects of Fe(II) and Fe(III) ions on secondary organic aerosol (SOA) formation, we conducted a series of photooxidation experiments with α-pinene and toluene in the presence of nitric oxides (NOx) with/without FeSO4 or Fe2(SO4)3 seed aerosols. The FeSO4 seed aerosols suppressed SOA formation, while Fe2(SO4)3 seed aerosols did not display a noticeable effect on SOA formation. We did not observe effects of FeSO4 and Fe2(SO4)3 seed aerosols on gas phase compounds, including ozone, NOx, and hydrocarbons (HCs). The negative effect of Fe(II)-containing seed aerosols on SOA formation due to the reduction of condensable compounds (CCs) generated from hydrocarbon oxidation is discussed. The mean molecular weight of CCs reduced by Fe(II) is tentatively estimated to be larger than 300, indicating a possibility that many of the CCs reduced by Fe(II) are oligomers. Reduction of oligomer precursors may interrupt the oligomerization of other aldehyde products. If Fe(II) regeneration from photoreduction of Fe(III) is considered, the estimated mean molecular weight of the CCs reduced would be smaller. However, the negligible effect of Fe(III)-containing seed aerosols on SOA formation indicates that Fe(III) photoreduction is negligible in our experiments.

  4. Marine aerosol formation from biogenic iodine emissions.

    PubMed

    O'Dowd, Colin D; Jimenez, Jose L; Bahreini, Roya; Flagan, Richard C; Seinfeld, John H; Hämeri, Kaarle; Pirjola, Liisa; Kulmala, Markku; Jennings, S Gerard; Hoffmann, Thorsten

    2002-06-01

    The formation of marine aerosols and cloud condensation nuclei--from which marine clouds originate--depends ultimately on the availability of new, nanometre-scale particles in the marine boundary layer. Because marine aerosols and clouds scatter incoming radiation and contribute a cooling effect to the Earth's radiation budget, new particle production is important in climate regulation. It has been suggested that sulphuric acid derived from the oxidation of dimethyl sulphide is responsible for the production of marine aerosols and cloud condensation nuclei. It was accordingly proposed that algae producing dimethyl sulphide play a role in climate regulation, but this has been difficult to prove and, consequently, the processes controlling marine particle formation remains largely undetermined. Here, using smog chamber experiments under coastal atmospheric conditions, we demonstrate that new particles can form from condensable iodine-containing vapours, which are the photolysis products of biogenic iodocarbons emitted from marine algae. Moreover, we illustrate, using aerosol formation models, that concentrations of condensable iodine-containing vapours over the open ocean are sufficient to influence marine particle formation. We suggest therefore that marine iodocarbon emissions have a potentially significant effect on global radiative forcing. PMID:12050661

  5. Long- and/or short-range transportation of local Asian aerosols in DRAGON-Osaka Experiment

    NASA Astrophysics Data System (ADS)

    Nakata, M.; Sano, I.; Mukai, S.; Holben, B. N.

    2013-12-01

    This work intends to demonstrate the spatial and temporal variation of atmospheric particles in East Asia, especially around AERONET (Aerosol Robotics Network) -Osaka site during Dragon Asia period in the spring of 2012, named Dragon-Osaka. It is known that the air pollution in East Asia becomes to be severe due to both the increasing emissions of the anthropogenic aerosols associated with economic growth and the complicated behavior of natural aerosols. Thus the precise observations of atmospheric particles in East Asia are desired. Osaka is the second big city in Japan and a typical Asian urban area. The population of the region is around 20 millions including neighbor prefectures. Therefore, air quality in the region is slightly bad compared to remote area due to industries and auto mobiles. In recent years, Asian dusts and anthropogenic small particles transported from China and cover those cities throughout year. AERONET Osaka site was established in 2002 on the campus of Kinki University. Nowadays, LIDAR (Light Detection and Ranging), an SPM sampler (SPM-613D, Kimoto Electric, Japan) and others are available on the roof of a building. The site data are useful for algorithm development of aerosol retrieval over busy city. On the other hand, human activities in this region also emit the huge amount of pollutions, thus it is needed to investigate the local distribution of aerosols in this region. In order to investigate change of aerosol properties, PM-individual analysis is made with scanning electron microscope (SEM) coupled with energy dispersive X-ray analyzer (EDX). SEM/EDX is an effective instrument to observe the surface microstructure and analyze the chemical composition of such materials as metals, powders, biological specimens, etc. We used sampling data from the SPM sampler at AERONET Osaka site. During a period of DRAGON-Asia, high concentrations of air pollutant were observed on the morning of March 11 in Fukue Island in the East China Sea. On the

  6. Ground based chemical characterization of submicron aerosol during the South American Biomass Burning Analysis (SAMBBA) field experiment

    NASA Astrophysics Data System (ADS)

    Brito, Joel; Artaxo, Paulo; Varanda Rizzo, Luciana; Johnson, Ben; Haywood, Jim; Longo, Karla; Freitas, Saulo; Coe, Hugh

    2013-04-01

    This work presents the results of an Aerosol Chemical Speciation Monitor (ACSM) which was successfully operated at a ground station in Porto Velho, Brazil, during the South American Biomass Burning Analysis (SAMBBA). SAMBBA is an international research project based on experimental and modeling activities designed to investigate the impacts of biomass burning emissions on climate, air quality and numerical weather prediction over South America. The measurement program was headed by the deployment of UK's Facility for Airborne Atmospheric Measurements (FAAM) BAe-146 research aircraft over Brazil during the dry season of 2012. The aircraft operation was coordinated with ground-based measurements at Porto Velho, operated by the University of Sao Paulo. Besides the aerosol chemical speciation, continuous measurements of aerosol size distribution and optical properties were carried out at the ground station, together with CO, CO2 and O3. Filters for trace elements measured by XRF and for OC/EC determined using a Sunset instrument were also collected at the ground based component of SAMBBA. The ACSM collected data for three weeks during September 2012. This period included a strong biomass burning event which showed a marked peak in f60, linked with Levoglucosan, a well-known biomass burning marker. During the biomass burning event, organics concentrations rose up to 80 μg/m3, black carbon close to 6 μg/m3 and CO mixing ratio above 2 ppmv. Fast biomass burning aerosol processing in the atmosphere could be observed through the relative contributions of C2H3O+ vs. CO2+ relative to total organic mass (f44 vs. f43). A clear diurnal variation throughout the sampling period has been observed for organic aerosols with a median peak of 9 μg/m3 at 04:00 LT and a minima of 5 μg/m3 at 18:00 LT. Preliminary results indicate that organics are responsible for 85% of PM1 non-refractory aerosols. The data set will allow the study of interactions between biomass burning and biogenic

  7. CALWATER-2 An Experiment Exploring the Roles of Atmospheric Rivers and Aerosols in Modulating U.S. West Coast Precipitation in a Changing Climate

    NASA Astrophysics Data System (ADS)

    Ralph, F. M.; Prather, K. A.; Cayan, D. R.; Dettinger, M. D.; Fairall, C. W.; Leung, L.; Rosenfeld, D.; Rutledge, S. A.; Spackman, J.; Waliser, D. E.

    2013-12-01

    Two phenomena that play key roles in the variability of the water supply and the incidence of extreme precipitation events along the West Coast of the United States are: 1) Atmospheric rivers (ARs), which deliver much of the precipitation associated with major storms along the U.S. West Coast, and 2) Aerosols--from local sources as well as those transported from remote continents--which can modulate western U.S. precipitation. A better understanding of these processes is needed to reduce uncertainties in weather predictions and climate projections of extreme precipitation and its effects, including the provision of beneficial water supply. This presentation summarizes science gaps associated with (1) the evolution and structure of ARs including cloud and precipitation processes and air-sea interaction, and (2) aerosol interaction with ARs and the impact on precipitation, including locally-generated aerosol effects on orographic precipitation along the U.S. West Coast. A set of science investigations, called CalWater 2, have been proposed over the next several years to fill these gaps including a targeted set of aircraft and ship-based measurements and associated evaluation of data over regions offshore of California and in the eastern Pacific for an intensive observing period between December 2014 and March 2015. DOE's Atmospheric Radiation Measurement (ARM) program and NOAA are coordinating on deployment of airborne and ship-borne facilities for this period, including a DOE-sponsored study called ACAPEX (ARM Cloud Aerosol and Precipitation Experiment) that was proposed in the context of CalWater 2. A broad 5-year vision of an interagency effort to address these science gaps will be presented, and informal input into this planning is being solicited through this presentation, including consideration of potential synergistic connections to other relevant activities. The CalWater 2 white paper was prepared by a team of meteorologists, hydrologists, climate scientists

  8. Aerosol industry success in reducing CFC (chlorofluorocarbon) propellant usage. Final report, January-September 1989

    SciTech Connect

    Nelson, T.P.; Wevill, S.L.

    1989-11-01

    The two-part report discusses the reduction of chlorofluorocarbon (CFC) propellant usage. Part I discusses the U.S. aerosol industry's experience in converting from CFC propellants to alternative aerosol formulations. Detailed examples of non-CFC formulations are provided for 28 categories of aerosol products. Hydrocarbon propellants, which cost less than CFCs, are most often selected as the propellants of choice unless special properties (e.g., increased solvency or reduced flammability) are needed. Dimethyl ether is the next most preferred CFC alternative although it is flammable and a strong solvent. Carbon dioxide, nitrous oxide, and nitrogen are inexpensive and widely available, but have been underused as aerosol propellants. Special equipment is often needed to add them to the aerosol containers.

  9. Containing Climate Change With Black Carbon Reductions: A Grand Challenge Field Experiment

    NASA Astrophysics Data System (ADS)

    Ramanathan, V.

    2009-12-01

    The manmade greenhouse gases that are now blanketing the planet is thick enough to push the system beyond the tipping point for several elements of the climate system such as the arctic sea ice and the Himalayan-Tibetan glaciers, to name a few. Even with a targeted reduction in CO2 emission of 50% by 2050, we would still be adding more than 50 ppm of CO2 and thicken the manmade blanket by another 30%. Fortunately there are scientific ways to contain the warming and these will be outlined. But these need a truly transformational and interdisciplinary approach that brings together social scientists, natural scientists, energy experts and engineers to develop effective mitigation pathways. Towards this goal an interdisciplinary team of academics, NGOs and intergovernmental organizations from US, Europe and India have developed Project Surya to drastically decrease emissions of the major non-CO2 climate warmers (soot, methane, ozone precursor gases) from rural areas in India and China. Surya will undertake the most comprehensive data collection, to-date, on the impact of reducing biomass burning on climate forcing, health and the wellbeing of rural inhabitants most of whom live under a dollar a day. The experiment thus offers the opportunity to field test our ideas and hypotheses about the impact of black carbon and brown clouds on dimming, the Asian monsoon and the melting of the Himalayan-Tibetan glaciers. The data from this soft ‘geo-engineering’ experiment is also anticipated to lead to a sustainable way of energy consumption for the roughly 4 billion who are forced to use solid bio-fuels for all of their energy needs.

  10. Molecular Characterization of S- and N-containing Organic Constituents in Ambient Aerosols by negative ion mode High-Resolution Nanospray Desorption Electrospray Ionization Mass Spectrometry: CalNex 2010 field study

    SciTech Connect

    O'Brien, Rachel E.; Laskin, Alexander; Laskin, Julia; Rubitschun, Caitlin L.; Surratt, Jason D.; Goldstein, Allen H.

    2014-11-27

    Samples of ambient aerosols from the 2010 California Research at the Nexus of Air Quality and Climate Change (CalNex) field study were analyzed using Nanospray Desorption Electrospray Ionization High Resolution Mass Spectrometry (nano-DESI/MS). Four samples per day were collected in Bakersfield, CA on June 20-24 with a collection time of 6 hours per sample. Four characteristic groups of organic constituents were identified in the samples: compounds containing carbon, hydrogen, and oxygen only (CHO), sulfur- (CHOS), nitrogen-(CHON), and both nitrogen- and sulfur-containing organics (CHONS). Within the groups, organonitrates, organosulfates, and nitroxy organosulfates were assigned based on accurate mass measurements and elemental ratio comparisons. Changes in the chemical composition of the aerosol samples were observed throughout the day. The number of observed CHO compounds increased in the afternoon samples, suggesting regional photochemical processing as a source. The average number of CHOS compounds had the smallest changes throughout the day, consistent with a more broadly distributed source. Both of the nitrogen-containing groups (CHON and CHONS) had greater numbers of compounds in the night and morning samples, indicating that nitrate radical chemistry was likely a source for those compounds. Most of the compounds were found in submicron particles. The size distribution of CHON compounds was bimodal. We conclude that the majority of the compounds observed were secondary in nature with both biogenic and anthropogenic sources.

  11. Damping analysis of a flexible cantilever beam containing an internal fluid channel: Experiment, modeling and analysis

    NASA Astrophysics Data System (ADS)

    Wang, Ya; Masoumi, Masoud; Gaucher-Petitdemange, Matthias

    2015-03-01

    Passive structural damping treatments have been applied with the use of high-viscosity fillings (in practice) and have been the focus of numerous research studies and papers. However, internal viscoelastic fluid leading to passive damping of flexible cantilever beams, has not yet been investigated in the literature. Although structures containing internal fluid channels provide multifunctional solutions to many engineering issues, they also raise damping control requests caused by unacceptable vibrations due to ambient environmental changes. In this paper, we examine ambient effects on damping properties of flexible cantilever beams, each conveying an internal high-viscosity fluid channel. Experiments are conducted to investigate how the internal fluids provide damping to the system under varied temperatures, frequencies and base-acceleration levels. While the vibration analysis of pipes conveying internal flow has been extensively studied, internal high-viscosity fluids in relation to passive damping of flexible cantilever beams and their ambient, environment-dependent behaviors have not been well-investigated. Originally motivated by research, which uses internal fluid channels to provide the cooling of multifunctional composite structures, we aim to research the damping behaviors of cantilever beams. We will conduct an experimental study and modeling analysis, examining the vibrations and frequency responses of the cantilever beams when filled with three types of internal fluids.

  12. Initial size distributions and hygroscopicity of indoor combustion aerosol particles

    SciTech Connect

    Li, W.; Hopke, P.K.

    1993-10-01

    Cigarette smoke, incense smoke, natural gas flames, propane fuel flames, and candle flames are contributors of indoor aerosol particles. To provide a quantitative basis for the modeling of inhaled aerosol deposition pattern, the hygroscopic growth of particles from these five sources as well as the source size distributions were measured. Because the experiments were performed on the bases of particles of single size, it provided not only the averaged particle`s hygroscopic growth of each source, but also the detailed size change for particles of different sizes within the whole size spectrum. The source particle size distribution measurements found that cigarette smoke and incense smoke contained particles in the size range of 100-700 nm, while the natural gas, propane, and candle flames generated particles between 10 and 100 nm. The hygroscopic growth experiments showed that these combustion aerosol particles could grow 10% to 120%, depending on the particle sizes and origins. 18 refs., 15 figs., 3 tabs.

  13. Enhanced Surface Photochemistry in Chloride-Nitrate Ion Aerosol Mixtures

    NASA Astrophysics Data System (ADS)

    Wingen, L. M.; Moskun, A. C.; Thomas, J. L.; Roeselova, M.; Tobias, D. J.; Finlayson-Pitts, B. J.

    2007-12-01

    Heterogeneous reactions of sea salt aerosol with various oxides of nitrogen often lead to replacement of chloride ion by nitrate ion. Photolysis of aqueous nitrate at wavelengths > 290 nm leads to the production of nitrogen dioxide, hydroxyl radicals and other oxidants. The photochemistry of aerosols containing NO3- and Cl-, however, has not been investigated. Aerosols containing mixtures of NaCl and NaNO3 were used as a model system for processed sea salt aerosol. Photolysis experiments (λmax = 306 nm) were performed in 55 L Teflon chambers that contained deliquesced aerosols and production of gas phase NO2 was measured as a function of time using chemiluminescence detection. Simple alkanes were added in some experiments to probe OH radical and Cl atom production. Molecular dynamics simulations were also carried out on mixed aqueous NaCl and NaNO3 slabs to help understand ion solvation in these mixed salt systems. The simulations showed that as the Cl- to NO3- ratio increases, nitrate ions are drawn toward the interface due to the large double layer of interfacial Cl- and subsurface Na+. The systems explored both experimentally and computationally included pure NaNO3 and mixtures of Cl- and NO3- in molar ratios of 1:9, 1:1, and 9:1. The photolysis experiments showed an enhanced yield of gas phase NO2 as the chloride to nitrate ratio increased. We attribute the observed enhanced NO2 yields to an increased interfacial concentration of under-coordinated nitrate ion as the ratio of Cl- to NO3- increases. The implications of these enhanced NO2 yields as sea salt aerosols become processed in the atmosphere will also be discussed.

  14. Heterogeneous Uptake of HO2 Radicals onto Atmospheric Aerosols

    NASA Astrophysics Data System (ADS)

    George, I. J.; Matthews, P. S.; Brooks, B.; Goddard, A.; Whalley, L. K.; Baeza-Romero, M. T.; Heard, D. E.

    2011-12-01

    containing metal ions, such as Cu and Fe. Humidity and aerosol pH did not significantly impact the reactive HO2 uptake. Preliminary experiments have also been conducted to study the temperature dependence of the uptake coefficients. These results suggest that particle phase and transition metal concentration are the most important factors to consider when modeling the impact of heterogeneous uptake onto aerosols as a HOx sink. References [1] R. Sommariva, A.-L.Haggerstone, L. J. Carpenter, N. Carslaw, D. J. Creasey, D. E. Heard, J. D. Lee, A. C. Lewis, M. J. Pilling, J. Zador, Atmos. Chem. Phys. 4 (2004) 839. [2] Y. Kanaya, R. Cao, S. Kato, Y. Miyakawa, Y. Kajii, H. Tanimoto, Y. Yokouchi, M. Mochida, K. Kawamura, H. J. Akimoto, Geophys. Res. 112 (2007) D11308.

  15. Meeting Review: Airborne Aerosol Inlet Workshop

    NASA Technical Reports Server (NTRS)

    Baumgardner, Darrel; Huebert, Barry; Wilson, Chuck

    1991-01-01

    Proceedings from the Airborne Aerosol Inlet Workshop are presented. The two central topics of discussion were the role of aerosols in atmospheric processes and the difficulties in characterizing aerosols. The following topics were discussed during the working sessions: airborne observations to date; identification of inlet design issues; inlet modeling needs and directions; objectives for aircraft experiments; and future laboratory and wind tunnel studies.

  16. Novel Measurements of Aerosol Particle Interfaces Using Biphasic Microfluidics

    NASA Astrophysics Data System (ADS)

    Metcalf, A. R.; Dutcher, C. S.

    2014-12-01

    Secondary organic aerosol (SOA) particles are nearly ubiquitous in the atmosphere and yet there remains large uncertainties in their formation processes and ambient properties. These particles are complex microenvironments, which can contain multiple interfaces due to internal aqueous-organic phase partitioning and to the external liquid-vapor surface. These aerosol interfaces can profoundly affect the fate of condensable organic compounds emitted into the atmosphere by altering the way in which organic vapors interact with the ambient aerosol. Aerosol interfaces affect particle internal structure, species uptake, equilibrium partitioning, activation to cloud condensation or ice nuclei, and optical properties. For example, organic thin films can shield the core of the aerosol from the ambient environment, which may disrupt equilibrium partitioning and mass transfer. To improve our ability to accurately predict the fate of SOA in the atmosphere, we must improve our knowledge of aerosol interfaces and their interactions with the ambient environment. Few technologies exist to accurately probe aerosol interfaces at atmospherically-relevant conditions. In this talk, a novel method using biphasic microscale flows will be introduced for generating, trapping, and perturbing complex interfaces at atmospherically relevant conditions. These microfluidic experiments utilize high-speed imaging to monitor interfacial phenomena at the microscale and are performed with phase contrast and fluorescence microscopy on a temperature-controlled inverted microscope stage. From these experiments, interfacial thermodynamic properties such as surface tension, rheological properties such as interfacial moduli, and kinetic properties such as mass transfer coefficients can be measured or inferred. Chemical compositions of the liquid phases studied here span a range of viscosities and include electrolyte and water soluble organic acid species often observed in the atmosphere, such as mixtures

  17. Aerosol chemistry in GLOBE

    NASA Technical Reports Server (NTRS)

    Clarke, Antony D.; Rothermel, Jeffry; Jarzembski, Maurice A.

    1993-01-01

    This task addresses the measurement and understanding of the physical and chemical properties of aerosol in remote regions that are responsible for aerosol backscatter at infrared wavelengths. Because it is representative of other clean areas, the remote Pacific is of extreme interest. Emphasis is on the determination size dependent aerosol properties that are required for modeling backscatter at various wavelengths and upon those features that may be used to help understand the nature, origin, cycling and climatology of these aerosols in the remote troposphere. Empirical relationships will be established between lidar measurements and backscatter derived from the aerosol microphysics as required by the NASA Doppler Lidar Program. This will include the analysis of results from the NASA GLOBE Survey Mission Flight Program. Additional instrument development and deployment will be carried out in order to extend and refine this data base. Identified activities include participation in groundbased and airborne experiments. Progress to date includes participation in, analysis of, and publication of results from Mauna Loa Backscatter Intercomparison Experiment (MABIE) and Global Backscatter Experiment (GLOBE).

  18. Measurements of the aerosol chemical composition and mixing state in the Po Valley using multiple spectroscopic techniques

    NASA Astrophysics Data System (ADS)

    Decesari, S.; Allan, J.; Plass-Duelmer, C.; Williams, B. J.; Paglione, M.; Facchini, M. C.; O'Dowd, C.; Harrison, R. M.; Gietl, J. K.; Coe, H.; Giulianelli, L.; Gobbi, G. P.; Lanconelli, C.; Carbone, C.; Worsnop, D.; Lambe, A. T.; Ahern, A. T.; Moretti, F.; Tagliavini, E.; Elste, T.; Gilge, S.; Zhang, Y.; Dall'Osto, M.

    2014-11-01

    residual layers but still originating in northern Italy, while a substantial fraction (41%) was due to the most aged aerosols imported from transalpine areas. The different meteorological regimes also affected the BC mixing state: in periods of enhanced stagnation and recirculation of pollutants, the number fraction of the BC-containing particles determined by ATOFMS was 75% of the total, while in the days of enhanced ventilation of the planetary boundary layer (PBL), such fraction was significantly lower (50%) because of the relative greater influence of non-BC-containing aerosol local sources in the Po Valley. Overall, a full internal mixing between BC and the non-refractory aerosol chemical components was not observed during the experiment in this environment.

  19. An intercomparison of SAGE and SBUV ozone observations for March and April 1979. [stratospheric aerosol and gas experiment solar backscatterd ultraviolet

    NASA Technical Reports Server (NTRS)

    Cunnold, D. M.; Pitts, M. C.; Trepte, C. R.

    1984-01-01

    Thirty-eight latitudinal cross sections of stratospheric ozone observed by the SAGE (Stratospheric Aerosol and Gas Experiment) and SBUV (Solar Backscattered Ultraviolet) satellite instruments on the same days in March and April 1979 and at approximately the same latitude are compared. Differences in the zonal-mean mixing ratios are found. At pressures less than 5 mbar, SAGE gives approximately 20 percent larger mixing ratios at tropical latitudes (after a correction has been applied for the expected diurnal variation of ozone). The uncorrelated portion of the SBUV variances are smaller than the SAGE noise variances at altitudes above 10 mbar, which indicates that the SBUV experiment should provide excellent detectability of longitudinal ozone variations.

  20. Chemical Composition of the Aerosol Fine Fraction during African Dust Events as part of the Dust ATtACk Experiment in the Caribbean Region

    NASA Astrophysics Data System (ADS)

    Vallejo, Pamela; Formenti, Paola; Desboeufs, Karine; Quiñones, Mariana; Chevaillier, Servanne; Santos, Stephanie; Andrews, Elizabeth; Ogren, John A.; Mayol-Bracero, Olga L.

    2015-04-01

    We present results on the assessment of aerosols' chemical composition at the atmospheric observatory of Cabezas de San Juan in Fajardo, Puerto Rico, during the summers of 2011 and 2012, where periods in the presence and absence of dust were studied under the framework of the Dust-ATtACk (Dust- Aging and Transport, from Africa to the Caribbean) experiment. Dust events were identified through observation and using air-mass back-trajectories, Saharan Air Layer images, measurements of aerosol optical thickness (AOT), in situ scattering and absorption coefficients, and chemical analyses. Results obtained for intense dust events were characterized by higher concentration of coarse particles, higher scattering and absorption coefficients (up to 100 Mm-1 and 5 Mm-1 at 550 and 530 nm, respectively), higher AOT (from 0.4 to 0.8) values, and higher concentration of elements associated with mineral dust (e.g., Si μ3 g/m3 compared to background concentrations of 0.15 μg/m3, obtained from XRF analysis). Elemental composition of the fine fraction (Dp < 1.8 μm), analyzed by ICP-OES, also yielded higher average concentrations during dust events of, for example, Fe (0.045 μg m-3, vs 0.016 μg m-3 during low or no dust). Detailed results of the submicron fraction composition for the carbonaceous aerosol (total carbon, organic carbon, black carbon), total nitrogen, the water-soluble organic carbon, water-soluble ions, and the elemental composition with their possible sources will be presented at the meeting.

  1. Analysis of a corporation's health care experience: implications for cost containment and disease prevention.

    PubMed

    Bernacki, E J; Tsai, S P; Reedy, S M

    1986-07-01

    This article presents the health care experience of 14,162 employees and their families, covered under a private third-party insurance plan of a large multinational corporation for the 1984 policy year. A total of $29.5 million was charged by health care providers to deliver medical care for the studied employees and their families. This amounted to $2,083 per employee and his/her family. Approximately 51% of the employees submitted claims, with females having greater utilization than males. The highest expenditures were for diseases of the circulatory system among adults (3.2 million or 23% for employees, $1.5 million or 14% for spouses). Among employees, neoplasms accounted for $1.4 million or 10% of costs, and musculoskeletal system $1.2 million or 9% of costs. Among spouses, pregnancy and diseases of the female reproductive system accounted for $1.2 million (12%) and $1.1 million (10%), respectively. Among dependents, the top three cost categories were mental disorders ($1.2 million or 24%), accident-related illnesses ($0.7 million or 14%), and diseases of the respiratory system ($0.6 million or 12%). Hospital care expenditures, including room and board, ancillary, and physician services, accounted for approximately 60% of total health care spending. The percentage of health care costs paid for by this insurance plan was 75% for active employees, 34% for retirees, 60% for female spouses, 38% for male spouses, and 64% for dependents. The analyses and parameters measured can be viewed as the first step toward the development of a health care cost containment and disease prevention strategy. PMID:3734919

  2. Highly stable aerosol generator

    DOEpatents

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

    1981-11-03

    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.

  3. Highly stable aerosol generator

    DOEpatents

    DeFord, Henry S.; Clark, Mark L.

    1981-01-01

    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.

  4. The new Mediterranean background monitoring station of Ersa, Cape Corsica: A long term Observatory component of the Chemistry-Aerosol Mediterranean Experiment (ChArMEx)

    NASA Astrophysics Data System (ADS)

    Dulac, Francois

    2013-04-01

    The Chemistry-Aerosol Mediterranean Experiment (ChArMEx, http://charmex.lsce.ipsl.fr/) is a French initiative supported by the MISTRALS program (Mediterranean Integrated Studies at Regional And Locals Scales, http://www.mistrals-home.org). It aims at a scientific assessment of the present and future state of the atmospheric environment in the Mediterranean Basin, and of its impacts on the regional climate, air quality, and marine biogeochemistry. The major stake is an understanding of the future of the Mediterranean region in a context of strong regional anthropogenic and climatic pressures. The target of ChArMEx is short-lived particulate and gaseous tropospheric trace species which are the cause of poor air quality events, have two-way interactions with climate, or impact the marine biogeochemistry. In order to fulfill these objectives, important efforts have been put in 2012 in order to implement the infrastructure and instrumentation for a fully equipped background monitoring station at Ersa, Cape Corsica, a key location at the crossroads of dusty southerly air masses and polluted outflows from the European continent. The observations at this station began in June 2012 (in the context of the EMEP / ACTRIS / PEGASOS / ChArMEx campaigns). A broad spectrum of aerosol properties is also measured at the station, from the chemical composition (off-line daily filter sampling in PM2.5/PM10, on-line Aerosol Chemical Speciation Monitor), ground optical properties (extinction/absorption/light scattering coeff. with 1-? CAPS PMex monitor, 7-? Aethalometer, 3-? Nephelometer), integrated and vertically resolved optical properties (4-? Cimel sunphotometer and LIDAR, respective), size distribution properties (N-AIS, SMPS, APS, and OPS instruments), mass (PM1/PM10 by TEOM/TEOM-FDMS), hygroscopicity (CCN), as well as total insoluble deposition. So far, real-time measurement of reactive gases (O3, CO, NO, NO2), and off-line VOC measurements (cylinders, cartridges) are also

  5. Organic aerosol formation photo-enhanced by the formation of secondary photosensitizers in aerosols.

    PubMed

    Aregahegn, Kifle Z; Nozière, Barbara; George, Christian

    2013-01-01

    Secondary organic aerosols (SOA), which are produced by the transformations of volatile organic compounds in the atmosphere, play a central role in air quality, public health, visibility and climate, but their formation and aging remain poorly characterized. This study evidences a new mechanism for SOA formation based on photosensitized particulate-phase chemistry. Experiments were performed with a horizontal aerosol flow reactor where the diameter growth of the particles was determined as a function of various parameters. In the absence of gas-phase oxidant, experiments in which ammonium sulfate seeds containing glyoxal were exposed to gas-phase limonene and UV light exhibited a photo-induced SOA growth. Further experiments showed that this growth was due to traces of imidazole-2-carboxaldehyde (IC) in the seeds, a condensation product of glyoxal acting as an efficient photosensitizer. Over a 19 min irradiation time, 50 nm seed particles containing this compound were observed to grow between 3.5 and 30 +/- 3% in the presence of either limonene, isoprene, alpha-pinene, beta-pinene, or toluene in concentrations between 1.8 and 352 ppmv. The other condensation products of glyoxal, imidazole (IM) and 2,2-bi1H-imidazole (BI), also acted as photosensitizer but with much less efficiency under the same conditions. In the atmosphere, glyoxal and potentially other gas precursors would thus produce efficient photosensitizers in aerosol and autophotocatalyze SOA growth. PMID:24601000

  6. Strategy to use the Terra Aerosol Information to Derive the Global Aerosol Radiative Forcing of Climate

    NASA Technical Reports Server (NTRS)

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

    2000-01-01

    Terra will derive the aerosol optical thickness and properties. The aerosol properties can be used to distinguish between natural and human-made aerosol. In the polar orbit Terra will measure aerosol only once a day, around 10:30 am. How will we use this information to study the global radiative impacts of aerosol on climate? We shall present a strategy to address this problem. It includes the following steps: - From the Terra aerosol optical thickness and size distribution model we derive the effect of aerosol on reflection of solar radiation at the top of the atmosphere. In a sensitivity study we show that the effect of aerosol on solar fluxes can be derived 10 times more accurately from the MODIS data than derivation of the optical thickness itself. Applications to data over several regions will be given. - Using 1/2 million AERONET global data of aerosol spectral optical thickness we show that the aerosol optical thickness and properties during the Terra 10:30 pass are equivalent to the daily average. Due to the aerosol lifetime of several days measurements at this time of the day are enough to assess the daily impact of aerosol on radiation. - Aerosol impact on the top of the atmosphere is only part of the climate question. The INDOEX experiment showed that addressing the impact of aerosol on climate, requires also measurements of the aerosol forcing at the surface. This can be done by a combination of measurements of MODIS and AERONET data.

  7. Mechanism for production of secondary organic aerosols and their representation in atmospheric models. Final report

    SciTech Connect

    Seinfeld, J.H.; Flagan, R.C.

    1999-06-07

    This document contains the following: organic aerosol formation from the oxidation of biogenic hydrocarbons; gas/particle partitioning of semivolatile organic compounds to model inorganic, organic, and ambient smog aerosols; and representation of secondary organic aerosol formation in atmospheric models.

  8. The physical state of UTLS aerosols

    NASA Astrophysics Data System (ADS)

    Peter, Th.; Colberg, C. A.; Corti, T.; Fueglistaler, S.; Hoyle, C. R.; Koop, T.; Krieger, U. K.; Luo, B. P.; Marcolli, C.

    2003-04-01

    This paper gives an overview of the present knowledge on the physical state of aerosols in the upper troposphere (UT) and lower stratosphere (LS). Are UTLS aerosols liquid, solid or mixed-phase? And how does ice nucleate in/on such aerosols? Good progress has been made towards a quantitative theory of homogeneous nucleation of ice in purely liquid solutions of arbitrary composition and concentration based on a volume-proportional description. Very recently it has been proposed that ice nucleation might be facilitated by the surface of aerosol droplets, rather than starting in the bulk, suggests a reversal of the traditional view. Nucleation rates would then be surface-proportional rather than volume-proportional, with potentially strong effects on cloud formation, ice number densities and dehydration of UT. However, laboratory and theoretical evidence is presented corroborating the traditional picture. Above the frost point UTLS aerosols remain either liquid or mixed-phase, e.g. solid letovicite plus the remaining liquid containing aqueous inorganic acids and organic compounds. Massive deliquescence and efflorescence point reductions are expected to occur upon mixing of miscible organic and inorganic components. Hence, for a reliable prediction of the phase composition of individual aerosol particles, the knowledge of the aerosol's mixing state is indispensable. By now little is known about the morphology of mixed-phase aerosols. Experiments suggest that the solid may be coated by liquid, or conversely that the liquid might be enclosed by the solid, possibly leading to different radiative and heterogeneous chemical properties. Knowledge on the impact of efflorescence or salting out on subsequent ice formation is at its infancy. The relative importance of all these processes, in particular of homogeneous and heterogeneous ice nucleation in the UTLS, depends crucially on gravity-wave-induced small-scale temperature fluctuations with typical amplitudes of 1-2 K and

  9. PROVING EXPERIMENTS AND ANALYSIS OF ROOFTOP HEAT SHIELD EXPERIMENT WITH WATER CONTAIN CONCRETE BOAD THAT USES ELEMENTARY SCHOOL BUILDING

    NASA Astrophysics Data System (ADS)

    Yamada, Hiroyuki; Tanaka, Akinori; 日根, 隆夫; Okuda, Yoshio; Koyama, Hiroyuki; Hada, Yuuichi

    In this study, the reduction effect of the heat inflow on the rooftop and the indoor thermal environment was measured by using the elementary school building, the rooftop of the bilding was covered with the water contain concrete boards. And, conserve energy effect and effectiveness for the indoor thermal environment improvement were evaluated. The effect of the decrease of the surface temperature and the slab side temperature at water contain concrete boad plot remarkably from the measurement result during the July-September of 2010, the temperatures decrease 22°C at the surface, 15°C at the waterproof layer surface that was caused compared with the gravel covered roof. The water contain concrete boards plot always drove the ceiling side temperature and the indoor temperature low as a result of comparing with the indoor condition of the control plot. The temperature fluctuate was small at time that opened the window and ventilated, and ventilation was discontinued, it became big temperatures fluctuate. The effect of the decrease of 0.5°C in PMV and 0.5 in WBGT was caused while the room had sealed up, and the effect of the decrease of 0.3 in WBGT was caused while the ventilated state.

  10. Photochemistry of Glyoxal in Wet Aerosols: Smog Chamber Study

    NASA Astrophysics Data System (ADS)

    Lim, Y. B.; Kim, H.; Turpin, B. J.

    2015-12-01

    Aqueous chemistry is an important pathway for the formation of secondary organic aerosol (SOA). Reaction vessel studies provide evidence that in the aqueous phase photooxidation of water soluble organic compounds (e.g., glyoxal, methylglyoxal) form multifunctional organic products and oligomers. In this work, we extend this bulk-phase chemistry to the condensed-phase chemistry that occurs in/on aerosols by conducting smog chamber experiments — photooxidation of ammonium sulfate and sulfuric acid aerosols containing glyoxal and hydrogen peroxide in the presence of NOx under dry/humid conditions. Particles were analyzed using ultra performance liquid chromatography coupled to quadrupole time-of-flight mass spectrometry (UPLC-Q-TOF-MS). In the irradiated chamber, photooxidation products of glyoxal as seen in reaction vessel experiments (e.g., oxalic acids and tartaric acids) were also formed in both ammonium sulfate aerosols and sulfuric acid aerosols at humid and even dry conditions. However, the major products were organosulfurs (CHOS), organonitrogens (CHON), and nitrooxy-organosulfates (CHONS), which were also dominantly formed in the dark chamber. These products were formed via non-radical reactions, which depend on acidity and humidity. However, the real-time profiles in the dark chamber and the irradiated chamber were very different, suggesting photochemistry substantially affects non-radical formation in the condensed phase.

  11. Capture of 0.1-μm aerosol particles containing viable H1N1 influenza virus by N95 filtering facepiece respirators.

    PubMed

    Harnish, Delbert A; Heimbuch, Brian K; Balzli, Charles; Choe, Melanie; Lumley, April E; Shaffer, Ronald E; Wander, Joseph D

    2016-01-01

    Nosocomial infections pose an escalating threat to both patients and healthcare workers (HCWs). A widely recommended device for individual respiratory protection, the N95 filtering facepiece respirator (FFR) has been shown to provide efficient filtration of inert particles larger and smaller than the nominal most-penetrating particle size (MPPS) range, 0.03-0.3 μm. Humans generate respiratory aerosols in the MPPS range, suggesting that short-range disease transmission could occur via small infectious particles. Data presented here show that the N95 FFR will afford a significant measure of protection against infectious particles as small as a bare H1N1 influenza virion, and that the capture mechanism does not discriminate in favor of, or against, biological particles. PMID:26554291

  12. Experiments to investigate direct containment heating phenomena with scaled models of the Calvert Cliffs Nuclear Power Plant

    SciTech Connect

    Blanchat, T.K.; Pilch, M.M.; Allen, M.D.

    1997-02-01

    The Surtsey Test Facility is used to perform scaled experiments simulating High Pressure Melt Ejection accidents in a nuclear power plant (NPP). The experiments investigate the effects of direct containment heating (DCH) on the containment load. The results from Zion and Surry experiments can be extrapolated to other Westinghouse plants, but predicted containment loads cannot be generalized to all Combustion Engineering (CE) plants. Five CE plants have melt dispersal flow paths which circumvent the main mitigation of containment compartmentalization in most Westinghouse PWRs. Calvert Cliff-like plant geometries and the impact of codispersed water were addressed as part of the DCH issue resolution. Integral effects tests were performed with a scale model of the Calvert Cliffs NPP inside the Surtsey test vessel. The experiments investigated the effects of codispersal of water, steam, and molten core stimulant materials on DCH loads under prototypic accident conditions and plant configurations. The results indicated that large amounts of coejected water reduced the DCH load by a small amount. Large amounts of debris were dispersed from the cavity to the upper dome (via the annular gap). 22 refs., 84 figs., 30 tabs.

  13. 21 CFR 510.301 - Records and reports concerning experience with animal feeds bearing or containing new animal...

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... animal feeds bearing or containing new animal drugs for which an approved medicated feed mill license... HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS NEW ANIMAL DRUGS Records and Reports § 510.301 Records and reports concerning experience with animal feeds bearing...

  14. 21 CFR 510.301 - Records and reports concerning experience with animal feeds bearing or containing new animal...

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS NEW ANIMAL DRUGS Records and Reports § 510.301 Records and reports concerning experience with animal feeds bearing or... animal feeds bearing or containing new animal drugs for which an approved medicated feed mill...

  15. 21 CFR 510.301 - Records and reports concerning experience with animal feeds bearing or containing new animal...

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS NEW ANIMAL DRUGS Records and Reports § 510.301 Records and reports concerning experience with animal feeds bearing or... animal feeds bearing or containing new animal drugs for which an approved medicated feed mill...

  16. 21 CFR 510.301 - Records and reports concerning experience with animal feeds bearing or containing new animal...

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS NEW ANIMAL DRUGS Records and Reports § 510.301 Records and reports concerning experience with animal feeds bearing or... animal feeds bearing or containing new animal drugs for which an approved medicated feed mill...

  17. Botany Facility. Thermal Control (TC) subsystem test report on experiment container of laboratory model and breadboard centrifuge

    NASA Astrophysics Data System (ADS)

    Fischer, W.

    1986-11-01

    The Botany Facility TC (Thermal Control or Thermocouple) subsystem was tested in the environmental laboratory. All data could be generated within the required accuracy and to the required extent. The TC-subsystems of the Laboratory Model and Experiment Container and Centrifuge were successfully tested.

  18. The presence of flour affects the efficacy of aerosolized insecticides used to treat the red flour beetle, Tribolium castaneum

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Experiments were conducted in tightly sealed pilot-scale warehouses to assess the efficacy of common aerosolized insecticides on all life stages of Tribolium castaneum when exposed in dishes containing 0 to 2 g of wheat flour either under pallets or out in the open. Petri dishes containing 0, 0.1, ...

  19. Global Aerosols

    Atmospheric Science Data Center

    2013-04-19

    ... sizes and from multiple sources, including biomass burning, mineral dust, sea salt and regional industrial pollution. A color scale is ... desert source region. Deserts are the main sources of mineral dust, and MISR obtains aerosol optical depth at visible wavelengths ...

  20. Headspace concentrations of explosive vapors in containers designed for canine testing and training: theory, experiment, and canine trials.

    PubMed

    Lotspeich, Erica; Kitts, Kelley; Goodpaster, John

    2012-07-10

    It is a common misconception that the amount of explosive is the chief contributor to the quantity of vapor that is available to trained canines. In fact, this quantity (known as odor availability) depends not only on the amount of explosive material, but also the container volume, explosive vapor pressure and temperature. In order to better understand odor availability, headspace experiments were conducted and the results were compared to theory. The vapor-phase concentrations of three liquid explosives (nitromethane, nitroethane and nitropropane) were predicted using the Ideal Gas Law for containers of various volumes that are in use for canine testing. These predictions were verified through experiments that varied the amount of sample, the container size, and the temperature. These results demonstrated that the amount of sample that is needed to saturate different sized containers is small, predictable and agrees well with theory. In general, and as expected, once the headspace of a container is saturated, any subsequent increase in sample volume will not result in the release of more vapors. The ability of canines to recognize and alert to differing amounts of nitromethane has also been studied. In particular, it was found that the response of trained canines is independent of the amount of nitromethane present, provided it is a sufficient quantity to saturate the container in which it is held. PMID:22421324

  1. Indian aerosols: present status.

    PubMed

    Mitra, A P; Sharma, C

    2002-12-01

    This article presents the status of aerosols in India based on the research activities undertaken during last few decades in this region. Programs, like International Geophysical Year (IGY), Monsoon Experiment (MONEX), Indian Middle Atmospheric Program (IMAP) and recently conducted Indian Ocean Experiment (INDOEX), have thrown new lights on the role of aerosols in global change. INDOEX has proved that the effects of aerosols are no longer confined to the local levels but extend at regional as well as global scales due to occurrence of long range transportation of aerosols from source regions along with wind trajectories. The loading of aerosols in the atmosphere is on rising due to energy intensive activities for developmental processes and other anthropogenic activities. One of the significant observation of INDOEX is the presence of high concentrations of carbonaceous aerosols in the near persistent winter time haze layer over tropical Indian Ocean which have probably been emitted from the burning of fossil-fuels and biofuels in the source region. These have significant bearing on the radiative forcing in the region and, therefore, have potential to alter monsoon and hydrological cycles. In general, the SPM concentrations have been found to be on higher sides in ambient atmosphere in many Indian cities but the NOx concentrations have been found to be on lower side. Even in the haze layer over Indian Ocean and surrounding areas, the NOx concentrations have been reported to be low which is not conducive of O3 formation in the haze/smog layer. The acid rain problem does not seem to exist at the moment in India because of the presence of neutralizing soil dust in the atmosphere. But the high particulate concentrations in most of the cities' atmosphere in India are of concern as it can cause deteriorated health conditions. PMID:12492171

  2. Estimation of lifetime of carbonaceous aerosol from open crop residue burning during Mount Tai Experiment 2006 (MTX2006)

    NASA Astrophysics Data System (ADS)

    Pan, X. L.; Kanaya, Y.; Wang, Z. F.; Komazaki, Y.; Taketani, F.; Akimoto, H.; Pochanart, P.; Liu, Y.

    2012-06-01

    Studying the emission ratios of carbonaceous aerosols (element carbon, EC, and organic carbon, OC) from open biomass burning helps to reduce uncertainties in emission inventories and provides necessary constraints for model simulations. We measured apparent elemental carbon (ECa) and OC concentrations at the summit of Mount Tai (Mt. Tai) during intensive open crop residue burning (OCRB) episodes using a Sunset OCEC analyzer. Equivalent black carbon (BCe) concentrations were determined using a Multiple Angle Absorption Photometer (MAAP). In the fine particle mode, OC and EC showed strong correlations (r > 0.9) with carbon monoxide (CO). Footprint analysis using the FLEXPART_WRF model indicated that OCRB in central east China (CEC) had a significant influence on ambient carbonaceous aerosol loadings at the summit of Mt. Tai. ΔECa/ΔCO ratios resulting from OCRB plumes were 14.3 ± 1.0 ng m-3 ppbv-1 at Mt. Tai. This ratio was more than three times those resulting from urban pollution in CEC, demonstrating that significant concentrations of soot particles were released from OCRB. ΔOC/ΔCO ratio from fresh OCRB plumes was found to be 41.9 ± 2.6 ng m-3 ppbv-1 in PM1. The transport time of smoke particles was estimated using the FLEXPART_WRF tracer model by releasing inert particles from the ground layer inside geographical regions where large numbers of hotspots were detected by a MODIS satellite sensor. Fitting regressions using the e-folding exponential function indicated that the removal efficiency of OC (normalized to CO) was much larger than that of ECa mass, with mean lifetimes of 27 h (1.1 days) for OC and 105 h (4.3 days) for ECa, respectively. The lifetime of black carbon estimated for the OCRB events in east China was comparably lower than the values normally adopted in the transport models. Short lifetime of organic carbon highlighted the vulnerability of OC to cloud scavenging in the presence of water-soluble organic species from biomass combustion.

  3. Experience report on coating concrete containment structures in a maintenance environment in power plants

    SciTech Connect

    Poncio, S.; Hall, D.

    1997-12-01

    Work experiences for coatings and lining applications in power plants are used to provide guidelines and recommendations for future projects. It should be emphasized that some of the work experiences are applicable to other industries, but the scope of this paper is primarily for maintenance concrete coating for immersion service in power plants. Also the importance of preplanning and scheduling of the concrete coating project is discussed.

  4. A synergetic approach for estimating the local direct aerosol forcing: Application to an urban zone during the Expérience sur Site pour Contraindre les Modèles de Pollution et de Transport d'Emission (ESCOMPTE) experiment

    NASA Astrophysics Data System (ADS)

    Roger, J. C.; Mallet, M.; Dubuisson, P.; Cachier, H.; Vermote, E.; Dubovik, O.; Despiau, S.

    2006-07-01

    A method dedicated to the investigation of direct radiative forcing of the main anthropogenic aerosol species (ammonium sulfate, black carbon, particulate organic matter) is presented. We computed the direct radiative aerosol forcing at the top of atmosphere (TOA), at the bottom of atmosphere (BOA), and into the atmospheric layer (ATM). The methodology is based on chemical, photometric, and satellite measurements. We first determined the optical properties of the main aerosol species and then computed their direct radiative impact at local scale. The method was applied to a periurban zone during the Expérience sur Site pour Contraindre les Modèles de Pollution et de Transport d'Emission experiment. Optical computations indicate that the single scattering albedo, for the total aerosol population in the external mixture, is equal to 0.83 ± 0.04 at 550 nm, indicative of a strong absorption of the solar radiation. At the same time the mean asymmetry parameter is equal to 0.59 ± 0.04, and the mean aerosol optical thickness is equal to 0.30 ± 0.02, at 550 nm. The anthropogenic urban aerosol layer reduces significantly the daily surface illumination (-24 W m-2 > ΔFBOA > -47.5 W m-2) by reflection to space (-6 W m-2 > ΔFTOA > -9 W m-2) and by absorption of the solar radiation into the atmosphere (17 W m-2 < ΔFATM < 39 W m-2). The available resulting energy in the atmospheric column heats the lowermost part of the atmosphere from 1.1°K d-1 to 2.8°K d-1. Our study shows that the black carbon particles have a large contribution to the BOA forcing (almost 50% of the total daily forcing), whereas the ammonium sulfate particles contribute only to about 10%. Conversely, the TOA daily forcing is mostly driven by the ammonium sulfate aerosol (around 50%).

  5. Using a laser aureole to study aerosols

    NASA Astrophysics Data System (ADS)

    Long, Brandon J. N.; Hook, D. A.; Pangle, Garrett E.; Hallen, Hans D.; Philbrick, C. R.

    2013-05-01

    Aerosol optical scattering experiments are often large, expensive, and provide poor control of dust uniformity and size distribution. The size distribution of such suspended atmospheric aerosols varies rapidly in time, since larger particles settle quickly. Even in large chambers, 10 micron particles settle in tens of seconds. We describe lab-scale experiments with stable particle distributions. A viscous colloidal solution can stabilize the particles for sufficient time to measure optical scattering properties. Colloids with different concentrations or size distributions enable nearly time independent studies of prepared distributions. We perform laser aureole scattering from a colloid containing a few percent by volume of Arizona Road Dust (ARD) in mineral oil and glycerin, and 1-micron polystyrene spheres in water. We discuss aureole analysis, the differences expected in scattering properties due to the index of refraction of the mineral oil medium versus air, and the impact of non-spherical shape on the scattering. This research demonstrates that particles suspended in a viscous medium can be used to simulate aerosol optical scattering in air, while enabling signal averaging, offering reproducibility, and easing problems resulting from parameter variations in studies of dust properties.

  6. Stratospheric aerosols and climatic change

    NASA Technical Reports Server (NTRS)

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

    1976-01-01

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

  7. HOUSTON URBAN PLUME STUDY, 1974. MICROSCOPICAL IDENTIFICATION OF COLLECTED AEROSOLS

    EPA Science Inventory

    An urban plume study was conducted in Houston during July 1974 to gain preliminary data on the concentration and composition of primary and secondary aerosols contributing to Houston's air pollution problem. Selected membrane filter samples containing urban aerosols were analyzed...

  8. Aerosol-halogen interaction: Change of physico-chemical properties of SOA by naturally released halogen species

    NASA Astrophysics Data System (ADS)

    Ofner, J.; Balzer, N.; Buxmann, J.; Grothe, H.; Krüger, H.; Platt, U.; Schmitt-Kopplin, P.; Zetzsch, C.

    2011-12-01

    Reactive halogen species are released by various sources like photo-activated sea-salt aerosol or salt pans and salt lakes. These heterogeneous release mechanisms have been overlooked so far, although their potential of interaction with organic aerosols like Secondary Organic Aerosol (SOA), Biomass Burning Organic Aerosol (BBOA) or Atmospheric Humic LIke Substances (HULIS) is completely unknown. Such reactions can constitute sources of gaseous organo-halogen compounds or halogenated organic particles in the atmospheric boundary layer. To study the interaction of organic aerosols with reactive halogen species (RHS), SOA was produced from α-pinene, catechol and guaiacol using an aerosol smog-chamber. The model SOAs were characterized in detail using a variety of physico-chemical methods (Ofner et al., 2011). Those aerosols were exposed to molecular halogens in the presence of UV/VIS irradiation and to halogens, released from simulated natural halogen sources like salt pans, in order to study the complex aerosol-halogen interaction. The heterogeneous reaction of RHS with those model aerosols leads to different gaseous species like CO2, CO and small reactive/toxic molecules like phosgene (COCl2). Hydrogen containing groups on the aerosol particles are destroyed to form HCl or HBr, and a significant formation of C-Br bonds could be verified in the particle phase. Carbonyl containing functional groups of the aerosol are strongly affected by the halogenation process. While changes of functional groups and gaseous species were visible using FTIR spectroscopy, optical properties were studied using Diffuse Reflectance UV/VIS spectroscopy. Overall, the optical properties of the processed organic aerosols are significantly changed. While chlorine causes a "bleaching" of the aerosol particles, bromine shifts the maximum of UV/VIS absorption to the red end of the UV/VIS spectrum. Further physico-chemical changes were recognized according to the aerosol size-distributions or the

  9. SAGE II aerosol correlative observations - Profile measurements

    NASA Technical Reports Server (NTRS)

    Osborn, M. T.; Rosen, J. M.; Mccormick, M. P.; Wang, Pi-Huan; Livinfston, J. M.

    1989-01-01

    Profiles of the aerosol extinction measurements from the Stratospheric Aerosol and Gas Experiment (SAGE) II are compared with profiles from five correlative experiments between November 1984 and July 1986. The correlative profiles were derived from six-channel dustsonde measurements and two-wavelength lidar backscatter data. The correlation between the dustsonde- and lidar-derived measurements and the SAGE II data is good, validating the SAGE II lower stratospheric aerosol extinction measurements.

  10. Aerosol in the Pacific troposphere

    NASA Technical Reports Server (NTRS)

    Clarke, Antony D.

    1989-01-01

    The use of near real-time optical techniques is emphasized for the measurement of mid-tropospheric aerosol over the Central Pacific. The primary focus is on measurement of the aerosol size distribution over the range of particle diameters from 0.15 to 5.0 microns that are essential for modeling CO2 backscatter values in support of the laser atmospheric wind sounder (LAWS) program. The measurement system employs a LAS-X (Laser Aerosol Spectrometer-PMS, Boulder, CO) with a custom 256 channel pulse height analyzer and software for detailed measurement and analysis of aerosol size distributions. A thermal preheater system (Thermo Optic Aerosol Descriminator (TOAD) conditions the aerosol in a manner that allows the discrimination of the size distribution of individual aerosol components such as sulfuric acid, sulfates and refractory species. This allows assessment of the relative contribution of each component to the BCO2 signal. This is necessary since the different components have different sources, exhibit independent variability and provide different BCO2 signals for a given mass and particle size. Field activities involve experiments designed to examine both temporal and spatial variability of these aerosol components from ground based and aircraft platforms.

  11. Aerosol Hygroscopicity Measured in Pristine and Polluted Conditions During the First Year of the GoAmazon 2014/15 Experiment

    NASA Astrophysics Data System (ADS)

    Barbosa, H. M.; Krüger, M. L.; Thalman, R.; Wang, J.; Pauliquevis, T.; Brito, J.; Poeschl, U.; Andreae, M. O.; Martin, S. T.; Artaxo, P.

    2015-12-01

    The effects of aerosol particles on cloud microphysical properties, cloud cover, precipitation, and regional climate are an important aspect of the climate system. The Amazon region is particularly susceptible to changes in number-diameter distributions of the atmospheric particle population because of the low background concentrations and high water vapor levels, indicating a regime of cloud properties that is highly sensitive to aerosol microphysics. This natural regime, different from most other continental areas worldwide, is expected to be perturbed by the interaction of the Manaus urban plume with the natural the natural environment. Studying the effects of this interaction on the cloud and aerosol life cycle is the main objective of the Green Ocean Amazon (GoAmazon) campaign taking place around Manaus-Brazil from January 2014 to December 2015. In this paper we compare the particle hygroscopicity calculated from measurements of size-resolved cloud condensation nuclei performed at three ground sites during the first year of the GoAmazon 2014/15 experiment. Site T3 is about 70 km downwind from Manaus experiencing urban polluted and background conditions; site T2 is just across the Rio Negro from Manaus and CCN measurements were performed there only from 15 August 2014 to 30 Jan 2015; and T0, at the Amazon Tall Tower Observatory (ATTO), is a pristine site about 200 km upwind from Manaus. Our results indicate a lower hygroscopicity under polluted conditions (mean kappa values around 0.14 to 0.16) than under clean conditions (mean kappa around 0.2 to 0.3). At the clean site, it was possible to identify peaks of large sea salt particles with organic coating, while small particles seems to be purely organic. The activation fraction and hygroscopicity will be compared and discussed as a function of particle size. The mean kappa at ATTO is 0.17+-0.05 (mean of June and September) when there is no impact from long range transport from Africa or fresh soot emissions

  12. Studies of organic aerosol and aerosol-cloud interactions

    NASA Astrophysics Data System (ADS)

    Duong, Hanh To

    Atmospheric aerosols can influence society and the environment in many ways including altering the planet's energy budget, the hydrologic cycle, and public health. However, the Fourth Assessment Report of the Intergovernmental Panel on Climate Change indicates that the anthropogenic radiative forcing associated with aerosol effects on clouds has the highest uncertainty in the future climate predictions. This thesis focuses on the nature of the organic fraction of ambient particles and how particles interact with clouds using a combination of tools including aircraft and ground measurements, models, and satellite data. Fine aerosol particles typically contain between 20 - 90% organic matter by mass and a major component of this fraction includes water soluble organic carbon (WSOC). Consequently, water-soluble organic species can strongly influence aerosol water-uptake and optical properties. However, the chemical composition of this fraction is not well-understood. PILS-TOC was used to characterize WSOC in ambient aerosol in Los Angeles, California. The spatial distribution of WSOC was found to be influenced by (i) a wide range of aerosol sources within this urban metropolitan area, (ii) transport of pollutants by the characteristic daytime sea breeze trajectory, (iii) topography, and (iv) secondary production during transport. Meteorology is linked with the strength of many of these various processes. Many methods and instruments have been used to study aerosol-cloud interactions. Each observational platform is characterized by different temporal/spatial resolutions and operational principles, and thus there are disagreements between different studies for the magnitude of mathematical constructs used to represent the strength of aerosol-cloud interactions. This work points to the sensitivity of the magnitude of aerosol-cloud interactions to cloud lifetime and spatial resolution of measurements and model simulations. Failure to account for above-cloud aerosol layers

  13. Results of direct containment heating integral experiments at 1/40th scale at Argonne National Laboratory

    SciTech Connect

    Binder, J.L.; McUmber, L.M.; Spencer, B.W.

    1993-09-01

    A series of integral tests have been completed that investigate the effect of scale and containment atmosphere initial composition on Direct Containment Heating (DCH) phenomena at 1/40 linear scale. A portion of these experiments were performed as counterparts to integral experiments conducted at 1/10th linear scale at Sandia National Laboratories. The tests investigated DCH phenomena in a 1/40th scale mockup of Zion Nuclear Power Plant geometry. The test apparatus was a scaled down version of the SNL apparatus and included models of the reactor vessel lower head, containment cavity, instrument tunnel, lower subcompartment structures and the upper dome. A High Pressure Melt Ejection (HPME) was produced using steam as a blowdown gas and iron-alumina thermite with chromium as a core melt simulant. The results of the counterpart experiments indicated no effect of scale on debris/gas heat transfer and debris metal oxidation with steam. However, the tests indicated a slight effect of scale on hydrogen combustion, the results indicating slightly more efficient combustion with increasing scale. The experiments demonstrated the effectiveness of the subcompartment structures in trapping debris exiting the cavity and preventing it from reaching the upper dome. The test results also indicated that a 50% air -- 50% steam atmosphere prevented hydrogen combustion. However, a 50% air - 50% nitrogen did not prevent hydrogen combustion in a HPME with all other conditions being nominally the same.

  14. Experiments to investigate the effect of flight path on direct containment heating (DCH) in the Surtsey test facility

    SciTech Connect

    Allen, M.D.; Pilch, M.; Griffith, R.O. ); Nichols, R.T. )

    1991-10-01

    The goal of the Limited Flight Path (LFP) test series was to investigate the effect of reactor subcompartment flight path length on direct containment heating (DCH). The test series consisted of eight experiments with nominal flight paths of 1, 2, or 8 m. A thermitically generated mixture of iron, chromium, and alumina simulated the corium melt of a severe reactor accident. After thermite ignition, superheated steam forcibly ejected the molten debris into a 1:10 linear scale the model of a dry reactor cavity. The blowdown steam entrained the molten debris and dispersed it into the Surtsey vessel. The vessel pressure, gas temperature, debris temperature, hydrogen produced by steam/metal reactions, debris velocity, mass dispersed into the Surtsey vessel, and debris particle size were measured for each experiment. The measured peak pressure for each experiment was normalized by the total amount of energy introduced into the Surtsey vessel; the normalized pressures increased with lengthened flight path. The debris temperature at the cavity exit was about 2320 K. Gas grab samples indicated that steam in the cavity reacted rapidly to form hydrogen, so the driving gas was a mixture of steam and hydrogen. These experiments indicate that debris may be trapped in reactor subcompartments and thus will not efficiently transfer heat to gas in the upper dome of a containment building. The effect of deentrainment by reactor subcompartments may significantly reduce the peak containment load in a severe reactor accident. 8 refs., 49 figs., 6 tabs.

  15. Review of models applicable to accident aerosols

    SciTech Connect

    Glissmeyer, J.A.

    1983-07-01

    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.

  16. Aerosol Behavior Log-Normal Distribution Model.

    2001-10-22

    HAARM3, an acronym for Heterogeneous Aerosol Agglomeration Revised Model 3, is the third program in the HAARM series developed to predict the time-dependent behavior of radioactive aerosols under postulated LMFBR accident conditions. HAARM3 was developed to include mechanisms of aerosol growth and removal which had not been accounted for in the earlier models. In addition, experimental measurements obtained on sodium oxide aerosols have been incorporated in the code. As in HAARM2, containment gas temperature, pressure,more » and temperature gradients normal to interior surfaces are permitted to vary with time. The effects of reduced density on sodium oxide agglomerate behavior and of nonspherical shape of particles on aerosol behavior mechanisms are taken into account, and aerosol agglomeration due to turbulent air motion is considered. Also included is a capability to calculate aerosol concentration attenuation factors and to restart problems requiring long computing times.« less

  17. Large outdoor chamber experiments and computer simulations: (I) Secondary organic aerosol formation from the oxidation of a mixture of d-limonene and α-pinene

    NASA Astrophysics Data System (ADS)

    Li, Qianfeng; Hu, Di; Leungsakul, Sirakarn; Kamens, Richard M.

    This work merges kinetic models for α-pinene and d-limonene which were individually developed to predict secondary organic aerosol (SOA) formation from these compounds. Three major changes in the d-limonene and α-pinene combined mechanism were made. First, radical-radical reactions were integrated so that radicals formed from both individual mechanisms all reacted with each other. Second, all SOA model species from both compounds were used to calculate semi-volatile partitioning for new semi-volatiles formed in the gas phase. Third particle phase reactions for particle phase α-pinene and d-limonene aldehydes, carboxylic acids, etc. were integrated. Experiments with mixtures of α-pinene and d-limonene, nitric oxide (NO), nitrogen dioxide (NO 2), and diurnal natural sunlight were carried out in a dual 270 m 3 outdoor Teflon film chamber located in Pittsboro, NC. The model closely simulated the behavior and timing for α-pinene, d-limonene, NO, NO 2, O 3 and SOA. Model sensitivities were tested with respect to effects of d-limonene/α-pinene ratios, initial hydrocarbon to NO x (HC 0/NO x) ratios, temperature, and light intensity. The results showed that SOA yield ( YSOA) was very sensitive to initial d-limonene/α-pinene ratio and temperature. The model was also used to simulate remote atmospheric SOA conditions that hypothetically could result from diurnal emissions of α-pinene, d-limonene and NO x. We observed that the volatility of the simulated SOA material on the aging aerosol decreased with time, and this was consistent with chamber observations. Of additional importance was that our simulation did not show a loss of SOA during the daytime and this was consistent with observed measurements.

  18. Design of experiments and multivariate analysis for evaluation of reversed-phase high-performance liquid chromatography with charged aerosol detection of sucrose caprate regioisomers.

    PubMed

    Lie, Aleksander; Wimmer, Reinhard; Pedersen, Lars Haastrup

    2013-03-15

    The use of step-down gradient elution profiles to improve separation of sucrose caprate regioisomers was investigated as part of the development of a quantitative RP-HPLC analysis method with charged aerosol detection. The investigation was conducted using design-of-experiments methodology and evaluated by multivariate regression analysis. This approach was proven to be useful for systematic method development in HPLC analysis. The gradient elution profiles were described by four variables - two concentration variables and two duration variables. The regression analysis showed that the concentration variables had the most significant effects on retention times, both as individual terms and as part of variable interactions. All the regioisomers exhibited non-linear relationships between eluent acetonitrile concentration and retention time with similar curvatures. Kendall rank correlation coefficients confirmed that the curvatures of the regioisomer curves were highly dependent on each other. Charged aerosol detection provided a mass-sensitivity of 10-100 ng for the sucrose fatty acid ester regioisomers. Resolution deviation (RD) was defined as an aggregate objective function for evaluating the separation of three specific sucrose caprate regioisomers with similar elution properties substituted at positions 6-, 3- and 1'-, respectively. The investigation resulted in the development of elution strategies for separation and quantitative RP-HPLC analysis of regioisomers of sucrose caprate with all eight sucrose caprate regioisomers successfully identified. Thus, resolutions above the level of adequacy for quantification, R(s)≥1.0, were achieved for all regioisomers, both with isocratic and gradient elution strategies. For isocratic elutions, the best separation was achieved with eluent acetonitrile concentration 34%. Gradient elution resulted in a similar RD, but decreased the analysis time by 7-28%. For the gradient resulting in the most desirable combination of

  19. Single-particle detection efficiencies of aerosol time-of-flight mass spectrometry during the North Atlantic marine boundary layer experiment.

    PubMed

    Dall'Osto, Manuel; Harrison, Roy M; Beddows, David C S; Freney, Evelyn J; Heal, Mathew R; Donovan, Robert J

    2006-08-15

    During the North Atlantic marine boundary layer experiment (NAMBLEX) sampling campaign at Mace Head, Ireland, both continental and maritime air masses were sampled. Aerosol was characterized both with a TSI 3800 time-of-flight mass spectrometer (ATOFMS) and a MOUDI microorifice impactor, and particle number counts were measured independently with an aerodynamic particle sizer. The data have been analyzed in order to elucidate factors determining the particle detection efficiencies of the ATOFMS. These are broken down according to the efficiency of the inlet system, the hit efficiency on particles which enter the sensing zone of the instrument and the sensitivity of the measured ion signal to the chemical species. A substantial matrix effect depending on the chemical composition of the aerosol sampled at the time was found, which is reflected in variations in the hit efficiency of particles entering the sensing zone of the instrument with the main desorption-ionization laser. This is in addition to the strong inverse power-law dependence of inlet transmission efficiency on particle diameter. The variation in hit efficiency with particle type is likely attributable to differences in the energetics of laser energy absorption, ablation, and ion formation. However, once variations in both inlet transmission and hit efficiencies are taken into account, no additional matrix dependence of ATOFMS response is required to obtain a linear relationship between the ion signal and the concentration of a particular chemical species. The observations show that a constant mass of material is ionized from each particle, irrespective of size. Consequently the integrated ion signal for a given chemical component and particle size class needs to be increased by a factor related to the cube of particle diameter in order to correlate with the airborne mass of that component. PMID:16955903

  20. Preliminary drop-tower experiments on liquid-interface geometry in partially filled containers at zero gravity

    NASA Technical Reports Server (NTRS)

    Smedley, G.

    1990-01-01

    Plexiglass containers with rounded trapezoidal cross sections were designed and built to test the validity of Concus and Finn's existence theorem (1974, 1983) for a bounded free liquid surface at zero gravity. Experiments were carried out at the NASA Lewis two-second drop tower. Dyed ethanol-water solutions and three immiscible liquid pairs, with one liquid dyed, were tested. High-speed movies were used to record the liquid motion. Liquid rose to the top of the smaller end of the containers when the contact angle was small enough, in agreement with the theory. Liquid interface motion demonstrated a strong dependence on physical properties, including surface roughness and contamination.

  1. Operational experience with ultrasonic bolt seals for safeguards containment of multielement bottles in THORP spent-fuel storage ponds

    SciTech Connect

    Hatt, C.D.; Reynolds, A.F.; Jeffrey, A.

    1995-12-31

    This paper describes the operational experience gained by British Nuclear Fuels Limited (BNFL) at the THORP spent-fuel storage facility in the application and verification of ultra-sonic bolt seals to light water reactor fuel containers and multielement bottles while in the storage ponds. Additionally, it discusses BNFL`s cooperation with the International Atomic Energy Agency, Euratom, and Joint Research Council-Ispra to facilitate the development and design modifications of the remote-handling tools used. Finally, it summarizes the benefits, from an operator`s point of view, of using the bolt seals as a safeguards/containment device.

  2. Uptake of all-trans retinoic acid–containing aerosol by inhalation to lungs in a guinea pig model system—A pilot study

    PubMed Central

    Schäffer, Michael W.; Roy, Somdutta Sinha; Mukherjee, Shyamali; Ong, David E.; Das, Salil K.

    2010-01-01

    Systemic therapies with retinoic acid (RA) can result in toxic side effects without yielding biologically effective levels in target tissues such as lung. The authors adapted a PARI LC Star nebulizer to create a tubular system for short-term inhalation treatment of guinea pigs using a water-miscible formulation of all-trans RA (ATRA) or vehicle. Based on the initial average weight, animals received an estimated average ATRA doses of either 0.32 mg·kg−1 (low dose, 1.4 mM), or 0.62 mg·kg−1 (medium dose, 2.8 mM), or 1.26 mg·kg−1 (high dose, 5.6 mM) 20 minutes per day for 6 consecutive days. This system led to a rise of ATRA levels in lung, but not liver or plasma. Cellular lung levels of retinol, retinyl palmitate, and retinyl stearate also appeared to be unaffected (245.6 ± 10.7, 47.4 ± 3.4, and 132.8 ± 7.7 ng·g−1 wet weight, respectively). The application of this aerosolized ATRA also induced a dose-dependent protein expression of the cellular retinol-binding protein 1 (CRBP-1) in lung, without apparent harmful side effects. PMID:21043991

  3. Global Aerosol Climatology Project.

    NASA Astrophysics Data System (ADS)

    Mishchenko, Michael; Penner, Joyce; Anderson, Donald

    2002-02-01

    This paper is concerned with uncertainties in the Advanced Very High Resolution Radiometer (AVHRR)-based retrieval of optical depth for heavy smoke aerosol plumes generated from forest fires that occurred in Canada due to a lack of knowledge on their optical properties (single-scattering albedo and asymmetry parameter). Typical values of the optical properties for smoke aerosols derived from such field experiments as Smoke, Clouds, and Radiation-Brazil (SCAR-B); Transport and Atmospheric Chemistry near the Equator-Atlantic (TRACE-A); Biomass Burning Airborne and Spaceborne Experiment in the Amazonas (BASE-A); and Boreal Ecosystem-Atmosphere Study (BOREAS) were first assumed for retrieving smoke optical depths. It is found that the maximum top-of-atmosphere (TOA) reflectance values calculated by models with these aerosol parameters are less than observations whose values are considerably higher. A successful retrieval would require an aerosol model that either has a substantially smaller asymmetry parameter (g < 0.4 versus g > 0.5), or higher single-scattering albedo ( 0.9 versus < 0.9), or both (e.g., g = 0.39 and = 0.91 versus g = 0.57 and = 0.87) than the existing models. Several potential causes were examined including small smoke particle size, low black carbon content, humidity effect, calibration errors, inaccurate surface albedo, mixture of cloud and aerosol layers, etc. A more sound smoke aerosol model is proposed that has a lower content of black carbon (mass ratio = 0.015) and smaller size (mean radius = 0.02 m for dry smoke particles), together with consideration of the effect of relative humidity. Ground-based observations of smoke suggest that for < 2.5 there is an increasing trend in and a decreasing trend in g with increases in , which is consistent with the results of satellite retrievals. Using these relationships as constraints, more plausible values of can be obtained for heavy smoke aerosol. The possibility of smoke-cloud mixtures is also

  4. Molecular characterization of S- and N-containing organic constituents in ambient aerosols by negative ion mode high-resolution Nanospray Desorption Electrospray Ionization Mass Spectrometry: CalNex 2010 field study

    NASA Astrophysics Data System (ADS)

    O'Brien, Rachel E.; Laskin, Alexander; Laskin, Julia; Rubitschun, Caitlin L.; Surratt, Jason D.; Goldstein, Allen H.

    2014-11-01

    Samples of ambient aerosols from the 2010 California Research at the Nexus of Air Quality and Climate Change (CalNex) field study were analyzed using negative ion mode Nanospray Desorption Electrospray Ionization High-Resolution Mass Spectrometry (nano-DESI/MS). Four samples per day (6 h each) were collected in Bakersfield, CA on 20-24 June. Four characteristic groups were identified: molecules composed of carbon, hydrogen, and oxygen only (CHO), sulfur- (CHOS), nitrogen- (CHON), and both nitrogen- and sulfur-containing organics (CHONS). The chemical formula and elemental ratios were consistent with the presence of organonitrates, organosulfate, and nitroxy organosulfates in the negative ion mode mass spectra. The number of observed CHO compounds increased in the afternoon samples, suggesting photochemical processing as a source. The average number of CHOS compounds had the smallest changes during the day, consistent with a more broadly distributed source. Both of the nitrogen-containing groups (CHONS and CHON) had greater numbers of compounds in the early morning (midnight to 6 A.M.) and night (6 P.M. to midnight) samples, respectively, consistent with nitrate radical chemistry as a likely source for those compounds. Most of the compounds were found in submicron particles. The size distribution of the number of CHON compounds was bimodal, potentially indicating two types of sources. We conclude that the majority of the compounds observed were secondary in nature with both biogenic and anthropogenic sources. These data are complementary to previous results from positive ion mode nano-DESI/MS analysis of a subset of the same samples providing a more complete view of aerosol chemical composition at Bakersfield.

  5. Experience in the use of hyperspectral data for the detection of vegetation containing narcotic substances

    NASA Astrophysics Data System (ADS)

    Sedelnikov, V. P.; Lukashevich, E. L.; Karpukhina, O. A.

    2014-12-01

    This paper provides the characteristics of an experimental sample of a hyperspectral videospectrometer Sokol-SCP and presents examples of the hyperspectral data received as a result of flight tests. The results of the detection of vegetation containing narcotic substances by spectral attributes using the obtained hyperspectral information are considered. The opportunity for using the hyperspectral data for detection of cannabis and papaver sites, including those in mixed crops with masking vegetation, is confirmed.

  6. Characterization of Florida red tide aerosol and the temporal profile of aerosol concentration

    PubMed Central

    Cheng, Yung Sung; Zhou, Yue; Pierce, Richard H.; Henry, Mike; Baden, Daniel G.

    2009-01-01

    Red tide aerosols containing aerosolized brevetoxins are produced during the red tide bloom and transported by wind to coastal areas of Florida. This study reports the characterization of Florida red tide aerosols in human volunteer studies, in which an asthma cohort spent 1 h on Siesta Beach (Sarasota, Florida) during aerosolized red tide events and non-exposure periods. Aerosol concentrations, brevetoxin levels, and particle size distribution were measured. Hourly filter samples were taken and analyzed for brevetoxin and NaCl concentrations. In addition, the aerosol mass concentration was monitored in real time. The results indicated that during a non-exposure period in October 2004, no brevetoxin was detected in the water, resulting in non-detectable levels of brevetoxin in the aerosol. In March 2005, the time-averaged concentrations of brevetoxins in water samples were moderate, in the range of 5–10 μg/L, and the corresponding brevetoxin level of Florida red tide aerosol ranged between 21 and 39 ng/m3. The temporal profiles of red tide aerosol concentration in terms of mass, NaCl, and brevetoxin were in good agreement, indicating that NaCl and brevetoxins are components of the red tide aerosol. By continuously monitoring the marine aerosol and wind direction at Siesta Beach, we observed that the marine aerosol concentration varied as the wind direction changed. The temporal profile of the Florida red tide aerosol during a sampling period could be explained generally with the variation of wind direction. PMID:19879288

  7. THAI Multi-Compartment Containment Test Program

    SciTech Connect

    Kanzleiter, T.; Poss, G.; Funke, F.; Allelein, H.J.

    2006-07-01

    The THAI experimental programme includes combined-effect investigations on thermal hydraulics, hydrogen, and fission product (iodine and aerosols) behaviour in LWR containments under severe accident conditions. An overview on the experiments performed up to now and on the future test program is presented, in combination with a selection of typical results to illustrate the versatility of the test facility and the broad variety of topics investigated. (authors)

  8. Bench-scale column experiments to study the containment of Cr(VI) in confined aquifers by bio-transformation.

    PubMed

    Shashidhar, T; Philip, Ligy; Murty Bhallamudi, S

    2006-04-17

    Bench-scale soil column experiments were conducted to study the effectiveness of Cr(VI) containment in confined aquifers using in situ bio-transformation. Batch adsorption studies were carried out to estimate the adsorption capacities of two different soils for Cr(VI) and Cr(III). Bio-kinetic parameters were evaluated for the enriched microbial system. The inhibition constant, evaluated using Monod's inhibition model, was found to be 11.46 mg/L of Cr(VI). Transport studies indicated that it would not be possible to contain Cr(VI) by adsorption alone. Transport and bio-transformation studies indicated that the pore velocity and the initial bio-mass concentration significantly affect the containment process. In situ bio-remediation is effective in the case of silty aquifers. Cr(VI) concentration of 25 mg/L was effectively contained within 60 cm of a confined silty aquifer. Cr(VI) containment could be achieved in sandy aquifers when the pore velocity was very low and the initial augmented bio-mass was high. A bio-barrier of approximately one meter width would be able to contain Cr(VI) if the initial Cr(VI) concentration is as much as 25 mg/L. PMID:16263213

  9. Investigation of aerosols released at high temperature from nuclear reactor core models

    NASA Astrophysics Data System (ADS)

    Pintér Csordás, A.; Matus, L.; Czitrovszky, A.; Jani, P.; Maróti, L.; Hózer, Z.; Windberg, P.; Hummel, R.

    2000-12-01

    Two experiments were performed to simulate severe reactor accident with air ingress into the hot reactor core. The model bundles contained nine PWR type fuel rods. Their cladding was pre-oxidised by argon-oxygen (test 1) and steam (test 2). The released aerosol was measured continuously by laser particle counters. Morphology and elemental composition of the aerosol particles were studied on samples collected by impactors and quartz filters. The highest aerosol release was detected at the steepest rise of the bundle temperature. A second increase of the aerosol release appeared at the cooling down period. Because of the higher maximum temperature at test 2 about two orders of magnitude more uranium was released than in test 1. The highest emission was found for tin at test 1 and for zirconium and iron at test 2.

  10. Responses of phytoplankton community to the input of different aerosols in the East China Sea

    NASA Astrophysics Data System (ADS)

    Meng, X.; Chen, Y.; Wang, B.; Ma, Q. W.; Wang, F. J.

    2016-07-01

    Atmospheric deposition can affect marine phytoplankton by supplying macronutrients and trace elements. We conducted mesocosm experiments by adding aerosols with different composition (dominated by mineral dust, biomass burning and high Cu, and secondary aerosol, respectively) to the surface seawater of the East China Sea. Chlorophyll a concentrations were found to be the highest and lowest after adding aerosols containing the highest Fe and dissolved inorganic nitrogen (DIN), respectively. The relative abundance of Haptophyceae increased significantly after adding mineral dust, whereas diatom, Dinophyceae and Cryptophyceae reached the maximum accompanied with the highest DIN. Our results suggest that Fe may be more important than DIN in promoting primary productivity in the sampled seawater. The input of mineral dust and anthropogenic aerosols may result in distinct changes of phytoplankton community structure.

  11. Wet scavenging limits the detection of aerosol effects on precipitation

    NASA Astrophysics Data System (ADS)

    Gryspeerdt, E.; Stier, P.; White, B. A.; Kipling, Z.

    2015-07-01

    Satellite studies of aerosol-cloud interactions usually make use of retrievals of both aerosol and cloud properties, but these retrievals are rarely spatially co-located. While it is possible to retrieve aerosol properties above clouds under certain circumstances, aerosol properties are usually only retrieved in cloud-free scenes. Generally, the smaller spatial variability of aerosols compared to clouds reduces the importance of this sampling difference. However, as precipitation generates an increase in spatial variability of aerosols, the imperfect co-location of aerosol and cloud property retrievals may lead to changes in observed aerosol-cloud-precipitation relationships in precipitating environments. In this work, we use a regional-scale model, satellite observations and reanalysis data to investigate how the non-coincidence of aerosol, cloud and precipitation retrievals affects correlations between them. We show that the difference in the aerosol optical depth (AOD)-precipitation relationship between general circulation models (GCMs) and satellite observations can be explained by the wet scavenging of aerosol. Using observations of the development of precipitation from cloud regimes, we show how the influence of wet scavenging can obscure possible aerosol influences on precipitation from convective clouds. This obscuring of aerosol-cloud-precipitation interactions by wet scavenging suggests that even if GCMs contained a perfect representation of aerosol influences on convective clouds, the difficulty of separating the "clear-sky" aerosol from the "all-sky" aerosol in GCMs may prevent them from reproducing the correlations seen in satellite data.

  12. A self-contained 3He refrigerator suitable for long duration balloon experiments

    NASA Astrophysics Data System (ADS)

    Masi, S.; Aquilini, E.; Cardoni, P.; de Bernardis, P.; Martinis, L.; Scaramuzzi, F.; Sforna, D.

    We describe the design, development and test of a self-contained 3He fridge, aimed to cool at ≲0.3 K a bolometric detection system with a hold time of two weeks. The system is robust and suitable for operation on a long-duration stratospheric balloon payload. A physical model of the fridge has been developed, which describes the measured hold time, limiting temperature and load curve of the fridge. The system has been flight tested successfully during two balloon flights of the BOOMERanG payload in summer 1997.

  13. [The experience of usage of alginate contain medication in complex therapy at children with GERD disease].

    PubMed

    Shcherbakov, P L; Lobanov, Iu F; Fugol, D S; Shilova, A V

    2009-01-01

    GERD Therapy at children is complicated task because of Physiological features of a children's body, which reflects on the processes of acid production, motility in upper gastro-intestinal tract and on the metabolism of pharmaceutical products. Some of these medications have age usage limitations due to lack of investigation of side effects in treatment of children. Usage of alginate contain medication in complex therapy of such pathological condition brings to not only fast and effective relief of such symptoms as heartburn, eructation and in positive endoscopy dynamics. PMID:20201310

  14. Synergy of Satellite-Surface Observations for Studying the Properties of Absorbing Aerosols in Asia

    NASA Technical Reports Server (NTRS)

    Tsay, Si-Chee

    2010-01-01

    Through interaction with clouds and alteration of the Earth's radiation budget, atmospheric aerosols significantly influence our weather and climate. Monsoon rainfalls, for example, sustain the livelihood of more than half of the world's population. Thus, understanding the mechanism that drives the water cycle and freshwater distribution is high-lighted as one of the major near-term goals in NASA's Earth Science Enterprise Strategy. Every cloud droplet/ice-crystal that serves as an essential element in portraying water cycle and distributing freshwater contains atmospheric aerosols at its core. In addition, the spatial and temporal variability of atmospheric aerosol properties is complex due to their dynamic nature. In fact, the predictability of the tropical climate system is much reduced during the boreal spring, which is associated with the peak season of biomass burning activities and regional/long-range transport of dust aerosols. Therefore, to accurately assess the impact of absorbing aerosols on regional-to-global climate requires not only modeling efforts but also continuous observations from satellites, aircraft, networks of ground-based instruments and dedicated field experiments. Since 1997 NASA has been successfully launching a series of satellites the Earth Observing System - to intensively study, and gain a better understanding of, the Earth as an integrated system. Through participation in many satellite remote-sensing/retrieval and validation projects over the years, we have gradually developed and refined the SMART (Surface-sensing Measurements for Atmospheric Radiative Transfer) and COMMIT (Chemical, Optical & Microphysical Measurements of In-situ Troposphere) mobile observatories, a suite of surface remote sensing and in-situ instruments that proved to be vital in providing high temporal measurements, which complement the satellite observations. In this talk, we will present SMART-COMMIT which has played key roles, serving as network or supersite

  15. Tropospheric Aerosols

    NASA Astrophysics Data System (ADS)

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

    2003-12-01

    It is widely believed that "On a clear day you can see forever," as proclaimed in the 1965 Broadway musical of the same name. While an admittedly beautiful thought, we all know that this concept is only figurative. Aside from Earth's curvature and Rayleigh scattering by air molecules, aerosols - colloidal suspensions of solid or liquid particles in a gas - limit our vision. Even on the clearest day, there are billions of aerosol particles per cubic meter of air.Atmospheric aerosols are commonly referred to as smoke, dust, haze, and smog, terms that are loosely reflective of their origin and composition. Aerosol particles have arisen naturally for eons from sea spray, volcanic emissions, wind entrainment of mineral dust, wildfires, and gas-to-particle conversion of hydrocarbons from plants and dimethylsulfide from the oceans. However, over the industrial period, the natural background aerosol has been greatly augmented by anthropogenic contributions, i.e., those produced by human activities. One manifestation of this impact is reduced visibility (Figure 1). Thus, perhaps more than in other realms of geochemistry, when considering the composition of the troposphere one must consider the effects of these activities. The atmosphere has become a reservoir for vast quantities of anthropogenic emissions that exert important perturbations on it and on the planetary ecosystem in general. Consequently, much recent research focuses on the effects of human activities on the atmosphere and, through them, on the environment and Earth's climate. For these reasons consideration of the geochemistry of the atmosphere, and of atmospheric aerosols in particular, must include the effects of human activities. (201K)Figure 1. Impairment of visibility by aerosols. Photographs at Yosemite National Park, California, USA. (a) Low aerosol concentration (particulate matter of aerodynamic diameter less than 2.5 μm, PM2.5=0.3 μg m-3; particulate matter of aerodynamic diameter less than 10

  16. Aerosol generation by raindrop impact on soil

    NASA Astrophysics Data System (ADS)

    Joung, Young Soo; Buie, Cullen R.

    2015-01-01

    Aerosols are investigated because of their significant impact on the environment and human health. To date, windblown dust and sea salt from sea spray through bursting bubbles have been considered the chief mechanisms of environmental aerosol dispersion. Here we investigate aerosol generation from droplets hitting wettable porous surfaces including various classifications of soil. We demonstrate that droplets can release aerosols when they influence porous surfaces, and these aerosols can deliver elements of the porous medium to the environment. Experiments on various porous media including soil and engineering materials reveal that knowledge of the surface properties and impact conditions can be used to predict when frenzied aerosol generation will occur. This study highlights new phenomena associated with droplets on porous media that could have implications for the investigation of aerosol generation in the environment.

  17. Characterization of ice-nucleating bacteria using on-line electron impact ionization aerosol mass spectrometry.

    PubMed

    Wolf, R; Slowik, J G; Schaupp, C; Amato, P; Saathoff, H; Möhler, O; Prévôt, A S H; Baltensperger, U

    2015-04-01

    The mass spectral signatures of airborne bacteria were measured and analyzed in cloud simulation experiments at the AIDA (Aerosol Interaction and Dynamics in the Atmosphere) facility. Suspensions of cultured cells in pure water were sprayed into the aerosol and cloud chambers forming an aerosol which consisted of intact cells, cell fragments and residual particles from the agar medium in which the bacteria were cultured. The aerosol particles were analyzed with a high-resolution time-of-flight aerosol mass spectrometer equipped with a newly developed PM2.5 aerodynamic lens. Positive matrix factorization (PMF) using the multilinear engine (ME-2) source apportionment was applied to deconvolve the bacteria and agar mass spectral signatures. The bacteria mass fraction contributed between 75 and 95% depending on the aerosol generation, with the remaining mass attributed to agar. We present mass spectra of Pseudomonas syringae and Pseudomonas fluorescens bacteria typical for ice-nucleation active bacteria in the atmosphere to facilitate the distinction of airborne bacteria from other constituents in ambient aerosol, e.g. by PMF/ME-2 source apportionment analyses. Nitrogen-containing ions were the most salient feature of the bacteria mass spectra, and a combination of C4 H8 N(+) (m/z 70) and C5 H12 N(+) (m/z 86) may be used as marker ions. PMID:26149110

  18. Aerosols in the Convective Boundary Layer: Radiation Effects on the Coupled Land-Atmosphere System

    NASA Astrophysics Data System (ADS)

    Barbaro, E.; Vila-Guerau Arellano, J.; Ouwersloot, H. G.; Schroter, J.; Donovan, D. P.; Krol, M. C.

    2013-12-01

    We investigate the responses of the surface energy budget and the convective boundary-layer (CBL) dynamics to the presence of aerosols using a combination of observations and numerical simulations. A detailed observational dataset containing (thermo)dynamic variables observed at CESAR (Cabauw Experimental Site for Atmospheric Research) and aerosol information from the European Integrated Project on Aerosol, Cloud, Climate, and Air Quality Interactions (IMPACT/EUCAARI) campaign is employed to design numerical experiments reproducing two prototype clear-sky days characterized by: (i) a well-mixed residual layer above a ground inversion and (ii) a continuously growing CBL. A large-eddy simulation (LES) model and a mixed-layer (MXL) model, both coupled to a broadband radiative transfer code and a land-surface model, are used to study the impacts of aerosol scattering and absorption of shortwave radiation on the land-atmosphere system. We successfully validate our model results using the measurements of (thermo)dynamic variables and aerosol properties for the two different CBL prototypes studied here. Our findings indicate that in order to reproduce the observed surface energy budget and CBL dynamics, information of the vertical structure and temporal evolution of the aerosols is necessary. Given the good agreement between the LES and the MXL model results, we use the MXL model to explore the aerosol effect on the land-atmosphere system for a wide range of optical depths and single scattering albedos. Our results show that higher loads of aerosols decrease irradiance, imposing an energy restriction at the surface. Over the studied well-watered grassland, aerosols reduce the sensible heat flux more than the latent heat flux. As a result, aerosols increase the evaporative fraction. Moreover, aerosols also delay the CBL morning onset and anticipate its afternoon collapse. If also present above the CBL during the morning transition, aerosols maintain a persistent near

  19. Four dimensional variational assimilation of in-situ and remote-sensing aerosol data

    NASA Astrophysics Data System (ADS)

    Nieradzik, L. P.; Elbern, H.

    2012-04-01

    Aerosols play an increasingly important role in atmospheric modelling. They have a strong influence on the radiative transfer balance and a significant impact on human health. Their origin is various and so are its effects. Most of the measurement sites in Europe account for an integrated aerosol load PMx (Particulate Matter of less than x μm in diameter) which does not give any qualitative information on the composition of the aerosol. Since very different constituents contribute to PMx, like e.g. mineral dust derived from desert storms or sea salt, it is necessary to make aerosol forecasts not only of load, but also type resolved. The method of four dimensional variational data assimilation (4Dvar) is a widely known technique to enhance forecast skills of CTMs (Chemistry-Transport-Models) by ingesting in-situ and, especially, remote-sensing measurements. The EURAD-IM (EURopean Air pollution Dispersion - Inverse Model), containing a full adjoint gas-phase model, has been expanded with an adjoint of the MADE (Modal Aerosol Dynamics model for Europe) to optimise initial and boundary values for aerosols using 4Dvar. A forward and an adjoint radiative transfer model is driven by the EURAD-IM as mapping between BLAOT (Boundary Layer Aerosol Optical Thickness) and internal aerosol species. Furthermore, its condensation scheme has been bypassed by an HDMR (High-Dimensional-Model-Representation) to ensure differentiability. In this study both in-situ measured PMx as well as satellite retrieved aerosol optical thicknesses have been assimilated and the effect on forecast performance has been investigated. The source of BLAOT is the aerosol retrieval system SYNAER (SYNergetic AErosol Retrieval) from DLR-DFD that retrieves AOT by making use of both AATSR/SCIAMACHY and AVHRR/GOME-2 data respectively. Its strengths are a large spatial coverage, near real-time availability, and the classification of five intrinsic aerosol species, namely water-solubles, water-insolubles, soot

  20. Critical experiments on an enriched uranium solution system containing periodically distributed strong thermal neutron absorbers

    SciTech Connect

    Rothe, R.E.

    1996-09-30

    A series of 62 critical and critical approach experiments were performed to evaluate a possible novel means of storing large volumes of fissile solution in a critically safe configuration. This study is intended to increase safety and economy through use of such a system in commercial plants which handle fissionable materials in liquid form. The fissile solution`s concentration may equal or slightly exceed the minimum-critical-volume concentration; and experiments were performed for high-enriched uranium solution. Results should be generally applicable in a wide variety of plant situations. The method is called the `Poisoned Tube Tank` because strong neutron absorbers (neutron poisons) are placed inside periodically spaced stainless steel tubes which separate absorber material from solution, keeping the former free of contamination. Eight absorbers are investigated. Both square and triangular pitched lattice patterns are studied. Ancillary topics which closely model typical plant situations are also reported. They include the effect of removing small bundles of absorbers as might occur during inspections in a production plant. Not taking the tank out of service for these inspections would be an economic advantage. Another ancillary topic studies the effect of the presence of a significant volume of unpoisoned solution close to the Poisoned Tube Tank on the critical height. A summary of the experimental findings is that boron compounds were excellent absorbers, as expected. This was true for granular materials such as Gerstley Borate and Borax; but it was also true for the flexible solid composed of boron carbide and rubber, even though only thin sheets were used. Experiments with small bundles of absorbers intentionally removed reveal that quite reasonable tanks could be constructed that would allow a few tubes at a time to be removed from the tank for inspection without removing the tank from production service.

  1. Impacts of 20th century aerosol emissions on the South Asian monsoon in the CMIP5 models

    NASA Astrophysics Data System (ADS)

    Turner, Andrew; Guo, Liang; Highwood, Eleanor

    2014-05-01

    Comparison of single-forcing varieties of 20th century historical experiments in a subset of models from the Fifth Coupled Model Intercomparison Project (CMIP5) reveals that South Asian summer monsoon rainfall increases towards the present day in GHG-only experiments with respect to pre-industrial levels, while it decreases in anthropogenic aerosol-only experiments. Comparison of these single-forcing runs with the all-forcings historical experiment suggests aerosol emissions have dominated South Asian monsoon rainfall trends in recent decades. By examining the 25 available all-forcings historical experiments, we show that models including aerosol indirect effects dominate this negative trend. Indeed, models including only the direct radiative effect of aerosol show an increase in monsoon rainfall, suggesting the dominance of increasing greenhouse gas emissions and planetary warming on monsoon rainfall in those models. The mechanism may be due to the indirect and direct effects acting in unison to suppress the monsoon, or to stronger local aerosol loading in the group of models containing indirect effects. The disparity between the two groups of models needs to be urgently investigated in the event that the suggested future decline in Asian anthropogenic aerosol emissions inherent to the representative concentration pathways (RCPs) used for future climate projection turns out to be optimistic.

  2. How much does sea spray aerosol organic matter impact clouds and radiation? Sensitivity studies in the Community Atmosphere Model

    NASA Astrophysics Data System (ADS)

    Burrows, S. M.; Liu, X.; Elliott, S.; Easter, R. C.; Singh, B.; Rasch, P. J.

    2015-12-01

    Submicron marine aerosol particles are frequently observed to contain substantial fractions of organic material, hypothesized to enter the atmosphere as part of the primary sea spray aerosol formed through bubble bursting. This organic matter in sea spray aerosol may affect cloud condensation nuclei and ice nuclei concentrations in the atmosphere, particularly in remote marine regions. Members of our team have developed a new, mechanistic representation of the enrichment of sea spray aerosol with organic matter, the OCEANFILMS parameterization (Burrows et al., 2014). This new representation uses fields from an ocean biogeochemistry model to predict properties of the emitted aerosol. We have recently implemented the OCEANFILMS representation of sea spray aerosol composition into the Community Atmosphere Model (CAM), and performed sensitivity experiments and comparisons with alternate formulations. Early results from these sensitivity simulations will be shown, including impacts on aerosols, clouds, and radiation. References: Burrows, S. M., Ogunro, O., Frossard, A. A., Russell, L. M., Rasch, P. J., and Elliott, S. M.: A physically based framework for modeling the organic fractionation of sea spray aerosol from bubble film Langmuir equilibria, Atmos. Chem. Phys., 14, 13601-13629, doi:10.5194/acp-14-13601-2014, 2014.

  3. Flight IV technical report for experiment 74-37 contained polycrystalline solidification in low-G

    NASA Technical Reports Server (NTRS)

    Papazian, J. M.; Kesselman, M.; Kattamis, T. Z.

    1977-01-01

    Experiments were performed to study the effect of a low-gravity environment on the columnar-to-equiaxed transition (CET) during polycrystalline solidification. Solutions of H2O-30 wt% NH4Cl and H2O-37 wt% NH4Cl were solidified in semicylindrical molds with radial heat extraction. Both solutions were quenched from the same soak temperature (90 C); the respective superheat temperatures were, therefore, approximately 57 and 23 C. The lower superheat resulted in a completely columnar structure, and the higher superheat resulted in a 1/3 columnar - 2/3 equiaxed microstructure; these results were independent of the relationship between heat flow direction and gravity. Grain multiplication mechanisms observed were showering, thermal inversion driven convection cells, and compositionally induced density inversion driven convection cells.

  4. Experiences in production and corrosion monitoring for a gas condensate field containing CO{sub 2}

    SciTech Connect

    Oberndorfer, M.; Dornstauder, K.; Brunner, W.

    1998-12-31

    The field Hoflein is located 10 km NW of Vienna. Gas condensate is produced out of 9 wells at the dew point of 28.1 MPa and 78 C. The reservoir fluid is lean but contains more than 16% CO{sub 2}. Lab test preceded the selection of the inhibitor for the carbon steel. Critical parts of the installations had 13%Cr steel. This paper describes the inhibitor testing procedures and the monitoring of the corrosion process by OMV Austria. The produced reservoir fluids and the critical components in the water (Cl, Fe, pH, inhibitor concentration) have been recorded over the years in various locations. Fluid analysis, corrosion coupon data visual inspection and caliper measurements of field installation document a high degree of protection. Recently the reservoir underwent a reevaluation in which the reserves could be doubled. This gave the incentive to produce at higher rates (from 8 to probably 16 m/s). Inhibitors of the 3rd generation that work even under high velocities were applied. For this case a test loop in the laboratory is described which allows for emulating the high velocity flow conditions that are planned in the field and where the inhibitors can be tested and selected.

  5. In situ vertical circulation column: Containment system for small-scale DNAPL field experiments

    SciTech Connect

    Sorel, D.; Cherry, J.A.; Lesage, S.

    1998-12-31

    The in situ vertical circulation column (ISVCC) is a cylindrical containment system consisting of an instrumented steel cylinder used for experimental ground water studies in sandy aquifers. Vertical flow is imposed inside the ISVCC. Although vertical wells are an option, the ISVCC installed in the Borden Aquifer is instrumented with horizontal wells and monitoring ports to avoid creating vertical preferential flow paths. Pure phase DNAPL (tetrachloroethene and 1,1,1-trichloroethane) was slowly pumped into two ports in the center of the column. Following this DNAPL injection, an aqueous solution of vitamin B{sub 12} and reduced titanium was circulated through the column to promote degradation of the solvents. Processes observed in the ISVCC included DNAPL distribution, dissolution, and degradation, and geochemical evolution of the aquifer. The ISVCC provides a convenient means for testing in situ technologies in the experimental stage or for selection of proven technologies to find the most effective at a specific site. It is inexpensive, easy to install, and maximizes control over flow distribution in a heterogeneous aquifer. Its application will be restricted where low hydraulic conductivity beds are present in the aquifer.

  6. Composition and diurnal variability of the natural Amazonian aerosol

    NASA Astrophysics Data System (ADS)

    Graham, Bim; Guyon, Pascal; Maenhaut, Willy; Taylor, Philip E.; Ebert, Martin; Matthias-Maser, Sabine; Mayol-Bracero, Olga L.; Godoi, Ricardo H. M.; Artaxo, Paulo; Meixner, Franz X.; Moura, Marcos A. Lima; Rocha, Carlos H. EçA. D'almeida; Grieken, Rene Van; Glovsky, M. Michael; Flagan, Richard C.; Andreae, Meinrat O.

    2003-12-01

    As part of the Large-Scale Biosphere-Atmosphere Experiment in Amazonia (LBA)-Cooperative LBA Airborne Regional Experiment (CLAIRE) 2001 campaign, separate day and nighttime aerosol samples were collected in July 2001 at a ground-based site in Amazonia, Brazil, in order to examine the composition and temporal variability of the natural "background" aerosol. A combination of analytical techniques was used to characterize the elemental and ionic composition of the aerosol. Major particle types larger than ˜0.5 μm were identified by electron and light microscopy. Both the coarse and fine aerosol were found to consist primarily of organic matter (˜70 and 80% by mass, respectively), with the coarse fraction containing small amounts of soil dust and sea-salt particles and the fine fraction containing some non-sea-salt sulfate. Coarse particulate mass concentrations (CPM ≈ PM10 - PM2) were found to be highest at night (average = 3.9 ± 1.4 μg m-3, mean night-to-day ratio = 1.9 ± 0.4), while fine particulate mass concentrations (FPM ≈ PM2) increased during the daytime (average = 2.6 ± 0.8 μg m-3, mean night-to-day ratio = 0.7 ± 0.1). The nocturnal increase in CPM coincided with an increase in primary biological particles in this size range (predominantly yeasts and other fungal spores), resulting from the trapping of surface-derived forest aerosol under a shallow nocturnal boundary layer and a lake-land breeze effect at the site, although active nocturnal sporulation may have also contributed. Associated with this, we observed elevated nighttime concentrations of biogenic elements and ions (P, S, K, Cu, Zn, NH4+) in the CPM fraction. For the FPM fraction a persistently higher daytime concentration of organic carbon was found, which indicates that photochemical production of secondary organic aerosol from biogenic volatile organic compounds may have made a significant contribution to the fine aerosol. Dust and sea-salt-associated elements/ions in the CPM fraction

  7. Hyaluron Filler Containing Lidocaine on a CPM Basis for Lip Augmentation: Reports from Practical Experience.

    PubMed

    Fischer, Tanja C; Sattler, Gerhard; Gauglitz, Gerd G

    2016-06-01

    Lip augmentation with hyaluronic acid fillers is established. As monophasic polydensified hyaluronic acid products with variable density, CPM-HAL1 (Belotero Balance Lidocaine, Merz Aesthetics, Raleigh, NC) and CPM-HAL2 (Belotero Intense Lidocaine, Merz Aesthetics, Raleigh, NC) are qualified for beautification and particularly natural-looking rejuvenation, respectively. The aim of this article was to assess the handling and outcome of lip augmentation using the lidocaine-containing hyaluronic acid fillers, CPM-HAL1 and CPM-HAL2. Data were documented from patients who received lip augmentation by means of beautification and/or rejuvenation using CPM-HAL1 and/or CPM-HAL2. Observation period was 4 months, with assessment of natural outcome, evenness, distribution, fluidity, handling, malleability, tolerability, as well as patient satisfaction and pain. A total of 146 patients from 21 German centers participated. Physicians rated natural outcome and evenness as good or very good for more than 95% of patients. Distribution, fluidity, handling, and malleability were assessed for both fillers as good or very good in more than 91% of patients. At every evaluation point, more than 93% of patients were very or very much satisfied with the product. A total of 125 patients (85.6%) experienced transient injection-related side effects. Pain intensity during the procedure was mild (2.72 ± 1.72 on the 0-10 pain assessment scale) and abated markedly within 30 minutes (0.42 ± 0.57). Lip augmentation with hyaluronic acid fillers produced a long-term cosmetic result. Due to the lidocaine content, procedural pain was low and transient. Accordingly, a high degree of patient satisfaction was achieved that was maintained throughout the observation period. PMID:27248026

  8. Investigation of Freeze-Linings in Copper-Containing Slag Systems: Part I. Preliminary Experiments

    NASA Astrophysics Data System (ADS)

    Fallah-Mehrjardi, Ata; Hayes, Peter C.; Jak, Evgueni

    2013-06-01

    Slag freeze-linings are increasingly used in industrial pyrometallurgical processes to insure that furnace integrity is maintained in aggressive high-temperature environments. Most previous studies of freeze-linings have analyzed the formation of slag deposits based solely on heat-transfer models. The focus of the present research is to determine the impact of slag chemistry and local process conditions on the microstructures, thickness, stability, and heat-transfer characteristics of the frozen deposit at steady-state conditions. The formation of the freeze-linings is studied under controlled laboratory conditions using an air-cooled "cold-finger" technique for Cu-Fe-Si-Al-O slag at equilibrium with metallic copper relevant to the industrial copper smelting processes. The phase assemblages and microstructures of the deposits formed in the cold-finger experiments differ significantly from those expected from phase equilibrium considerations. The freeze-lining deposits have been found, in general, to consist of several layers. Starting from the cold finger, these layers consist of glass; glass with microcrystalline precipitates; closed crystalline layer; and open crystalline layer. Even at steady-state conditions, there was no primary phase sealing layer of delafossite [Cu2O · (Al, Fe)2O3] present at the deposit/liquid interface—these observations differ markedly from those expected from phase equilibrium considerations. The findings have significant practical implications, and potential for the improved design and operation of industrial metallurgical furnaces.

  9. AEROSOL CHEMICAL CHARACTERISTION ON BOARD THE DOE G1 AIRCRAFT USING A PARTICLE INTO LIQUID SAMPLER DURING THE TEXAQS 2000 EXPERIMENT.

    SciTech Connect

    LEE,Y.N.; SONG,Z.; LIU,Y.; DAUM,P.; WEBER,R.; ORSINI,D.; LAULAINEN,N.; HUBBE,J.; MORRIS,V.

    2001-01-13

    Knowledge of aerosol chemical composition is key to understanding a number of properties of ambient aerosol particles including sources, size/number distribution, chemical evolution, optical properties and human health effects. Although filter based techniques have been widely used to determine aerosol chemical constituents, they generally cannot provide sufficiently fast time resolution needed to investigate sources and chemical evolution that effect aerosol chemical, size and number changes. In order to gain an ability to describe and predict the life cycles of ambient aerosols as a basis for ambient air quality control, fast and sensitive determination of the aerosol chemical composition must be made available. To help to achieve this goal, we deployed a newly developed technique, referred to as PILS (particle-into-liquid-sampler), on the DOE G1 aircraft during the 2000 Texas Air Quality Study (TexAQS 2000) to characterize the major ionic species of aerosol particles with aerodynamic size smaller than 2.5 {micro}m (PM 2.5). The results obtained are examined in the context of other simultaneously collected data for insights into the measurement capability of the PILS system.

  10. Extraction and Quantitation of FD&C Red Dye #40 from Beverages Containing Cranberry Juice: A College-Level Analytical Chemistry Experiment

    ERIC Educational Resources Information Center

    Rossi, Henry F., III; Rizzo, Jacqueline; Zimmerman, Devon C.; Usher, Karyn M.

    2012-01-01

    A chemical separation experiment can be an interesting addition to an introductory analytical chemistry laboratory course. We have developed an experiment to extract FD&C Red Dye #40 from beverages containing cranberry juice. After extraction, the dye is quantified using colorimetry. The experiment gives students hands-on experience in using solid…

  11. Characterization of aerosols produced by surgical procedures

    SciTech Connect

    Yeh, H.C.; Muggenburg, B.A.; Lundgren, D.L.; Guilmette, R.A.; Snipes, M.B.; Jones, R.K.; Turner, R.S.

    1994-07-01

    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.

  12. Ice nucleation by soil dust compared to desert dust aerosols

    NASA Astrophysics Data System (ADS)

    Moehler, O.; Steinke, I.; Ullrich, R.; Höhler, K.; Schiebel, T.; Hoose, C.; Funk, R.

    2015-12-01

    A minor fraction of atmospheric aerosol particles, so-called ice-nucleating particles (INPs), initiates the formation of the ice phase in tropospheric clouds and thereby markedly influences the Earth's weather and climate systems. Whether an aerosol particle acts as an INP depends on its size, morphology and chemical compositions. The INP fraction of certain aerosol types also strongly depends on the temperature and the relative humidity. Because both desert dust and soil dust aerosols typically comprise a variety of different particles, it is difficult to assess and predict their contribution to the atmospheric INP abundance. This requires both accurate modelling of the sources and atmospheric distribution of atmospheric dust components and detailed investigations of their ice nucleation activities. The latter can be achieved in laboratory experiments and parameterized for use in weather and climate models as a function of temperature and particle surface area, a parameter called ice-nucleation active site (INAS) density. Concerning ice nucleation activity studies, the soil dust is of particular interest because it contains a significant fraction of organics and biological components, both with the potential for contributing to the atmospheric INP abundance at relatively high temperatures compared to mineral components. First laboratory ice nucleation experiments with a few soil dust samples indicated their INP fraction to be comparable or slightly enhanced to that of desert dust. We have used the AIDA (Aerosol Interaction and Dynamics in the Atmosphere) cloud simulation chamber to study the immersion freezing ability of four different arable soil dusts, sampled in Germany, China and Argentina. For temperatures higher than about -20°C, we found the INP fraction of aerosols generated from these samples by a dry dispersion technique to be significantly higher compared to various desert dust aerosols also investigated in AIDA experiments. In this contribution, we

  13. Photoacoustic insight for aerosol light absorption aloft from meteorological aircraft and comparison with particle soot absorption photometer measurements: DOE Southern Great Plains climate research facility and the coastal stratocumulus imposed perturbation experiments

    NASA Astrophysics Data System (ADS)

    Arnott, W. Patrick; Walker, John W.; Moosmüller, Hans; Elleman, Robert A.; Jonsson, Haflidi H.; Buzorius, Gintautas; Conant, William C.; Flagan, Richard C.; Seinfeld, John H.

    2006-03-01

    Aerosol light absorption can be intense close to local sources such as wildland and oil fires, with smoke that disperses into the boundary layer and, with enough lift, into the upper atmosphere where it may be transported around the globe. Filter-based methods such as the Particle Soot Absorption Photometer (PSAP) are most commonly used to quantify aerosol light absorption aloft. This paper reports first measurements of aerosol light absorption aloft with photoacoustic instrumentation (PA). Three examples of aerosol light absorption are presented. The first one illustrates a case of detached layers aloft arising from intercontinental, interoceanic transport of smoke from wildland fires in Siberia to the North American continent and the measurement campaign held at the Department of Energy Atmospheric Radiation Measurement Program Climate Research Facility in north central Oklahoma. Then, two examples of intense local fire smoke light absorption from the Coastal Stratocumulus Imposed Perturbation Experiment near Marina, California, USA, are presented. The first local fire was an oil fire burning in a storage tank near Moss Landing, California, USA, and smoke from this fire was very dark, indicating a low single scattering albedo. By contrast, the second local fire was predominantly burning wood, vegetation, and structures near Fort Ord in Marina, California, USA, and the smoke was very bright, indicating a high single scattering albedo. In all examples, PA measurements at 676 nm were compared with those from a PSAP modified to measure at three wavelengths, including 660 nm.

  14. Direct containment heating experiments in Zion Nuclear Power Plant Geometry using prototypic core materials, the U2 test

    SciTech Connect

    Binder, J.L.; McUmber, L.M.; Spencer, B.W.

    1993-05-01

    A third Direct Containment Heating (DCH) experiments has been completed which utilizes prototypic core materials. The reactor material tests are a follow on to the Integral Effects Testing (IET) DCH program. The IET series of tests primarily addressed the effect of scale on DCH phenomena. This was accomplished by completing a series of counterpart tests in 1/40 and 1/10th linear scale DCH facilities at Argonne National Laboratory (ANL) and Sandia National Laboratories (SNL), respectively. The IET experiments modeled the Zion Nuclear Power Plant Geometry. The scale models included representations of the primary system volume, RPV lower head, cavity and instrument tunnel, and the lower containment structures. The experiments were steam driven at nominally 6.2 MPa. Iron-alumina thermite with chromium was used as a core melt simulant in the IET experiments. While the IET experiments at ANL and SNL provided useful data on the effect of scale on DCH phenomena, a significant question concerns the potential experiment distortions introduced by the use of non-prototypic iron/alumina thermite. Therefore, further testing with prototypic materials has been carried out at ANL. A prototypic core melt was produced for the experiment by first mixing powders of uranium, zirconium, iron oxide (Fe{sub 2}O{sub 3}), and chromium trioxide (CrO{sub 3}). When ignited the powders react exothermically to produce a molten mixture. The amounts of each powder were selected to produce the anticipated composition for a core melt following a station blackout: 57.8 mass% UO{sub 2} 10.5 mass% ZrO{sub 2} 14.3 mass% Fe, 13.7 mass% Zr, and 3.7 mass% Cr. Development tests measured the initial melt temperature to be in the range of 2600 - 2700 K. The total thermal specific energy content of the melt at 2700 K is 1.2 MJ/kg compared to 2.25 MJ/kg for the iron-alumina simulant at its measured initial temperature of 2500 K.

  15. A brief overview of the Chemistry-Aerosol Mediterranean Experiment (ChArMEx) database and campaign operation centre (ChOC)

    NASA Astrophysics Data System (ADS)

    Ferré, Hélène; Dulac, François; Belmahfoud, Nizar; Brissebrat, Guillaume; Cloché, Sophie; Descloitres, Jacques; Fleury, Laurence; Focsa, Loredana; Henriot, Nicolas; Ramage, Karim; Vermeulen, Anne

    2016-04-01

    Initiated in 2010 in the framework of the multidisciplinary research programme MISTRALS (Mediterranean Integrated Studies at Regional and Local Scales; http:www.mistrals-home.org), the Chemistry-Aerosol Mediterranean Experiment (ChArMEx, http://charmex.lsce.ipsl.fr/) aims at federating the scientific community for an updated assessment of the present and future state of the atmospheric environment in the Mediterranean Basin, and of its impacts on the regional climate, air quality, and marine biogeochemistry. The project combines mid- and long-term monitoring, intensive field campaigns, use of satellite data, and modelling studies. In this presentation we provide an overview of the campaign operation centre (http://choc.sedoo.fr/) and project database (http://mistrals.sedoo.fr/ChArMEx), at the end of the first experimental phase of the project that included a series of large campaigns based on airborne means (including balloons and various aircraft) and a network of surface stations. Those campaigns were performed mainly in the western Mediterranean basin in the summer of 2012, 2013 and 2014 with the help of the ChArMEx Operation Centre (ChOC), an open web site that has the objective to gather and display daily quick-looks from model forecasts and near-real time in situ and remote sensing observations of physical and chemical weather conditions relevant for the everyday campaign operation decisions. The ChOC is also useful for post campaign analyses and can be completed with a number of quick-looks of campaign results obtained later in order to offer an easy access to, and comprehensive view of all available data during the campaign period. The items included are selected according to the objectives and location of the given campaigns. The second experimental phase of ChArMEx from 2015 on is more focused on the eastern basin. In addition, the project operation centre is planned to be adapted for a joint MERMEX-ChArMEx oceanographic cruise (PEACETIME) for a study at

  16. A brief overview of the Chemistry-Aerosol Mediterranean Experiment (ChArMEx) database and campaign operation centre (ChOC)

    NASA Astrophysics Data System (ADS)

    Ferré, Hélène; Dulac, François; Belmahfoud, Nizar; Brissebrat, Guillaume; Cloché, Sophie; Descloitres, Jacques; Fleury, Laurence; Focsa, Loredana; Henriot, Nicolas; Ramage, Karim; Vermeulen, Anne

    2016-04-01

    Initiated in 2010 in the framework of the multidisciplinary research programme MISTRALS (Mediterranean Integrated Studies at Regional and Local Scales; http:www.mistrals-home.org), the Chemistry-Aerosol Mediterranean Experiment (ChArMEx, http://charmex.lsce.ipsl.fr/) aims at federating the scientific community for an updated assessment of the present and future state of the atmospheric environment in the Mediterranean Basin, and of its impacts on the regional climate, air quality, and marine biogeochemistry. The project combines mid- and long-term monitoring, intensive field campaigns, use of satellite data, and modelling studies. In this presentation we provide an overview of the campaign operation centre (http://choc.sedoo.fr/) and project database (http://mistrals.sedoo.fr/ChArMEx), at the end of the first experimental phase of the project that included a series of large campaigns based on airborne means (including balloons and various aircraft) and a network of surface stations. Those campaigns were performed mainly in the western Mediterranean basin in the summer of 2012, 2013 and 2014 with the help of the ChArMEx Operation Centre (ChOC), an open web site that has the objective to gather and display daily quick-looks from model forecasts and near-real time in situ and remote sensing observations of physical and chemical weather conditions relevant for the everyday campaign operation decisions. The ChOC is also useful for post campaign analyses and can be completed with a number of quick-looks of campaign results obtained later in order to offer an easy access to, and comprehensive view of all available data during the campaign period. The items included are selected according to the objectives and location of the given campaigns. The second experimental phase of ChArMEx from 2015 on is more focused on the eastern basin. In addition, the project operation centre is planned to be adapted for a joint MERMEX-ChArMEx oceanographic cruise (PEACETIME) for a study at

  17. Comparison of the impact of volcanic eruptions and aircraft emissions on the aerosol mass loading and sulfur budget in the stratosphere

    NASA Technical Reports Server (NTRS)

    Yue, Glenn K.; Poole, Lamont R.

    1992-01-01

    Data obtained by the Stratospheric Aerosol and Gas Experiment (SAGE) 1 and 2 were used to study the temporal variation of aerosol optical properties and to assess the mass loading of stratospheric aerosols from the eruption of volcanos Ruiz and Kelut. It was found that the yearly global average of optical depth at 1.0 micron for stratospheric background aerosols in 1979 was 1.16 x 10(exp -3) and in 1989 was 1.66 x 10(exp -3). The eruptions of volcanos Ruiz and Kelut ejected at least 5.6 x 10(exp 5) and 1.8 x 10(exp 5) tons of materials into the stratosphere, respectively. The amount of sulfur emitted per year from the projected subsonic and supersonic fleet is comparable to that contained in the background aerosol particles in midlatitudes from 35 deg N to 55 deg N.

  18. The evaluation of a shuttle borne lidar experiment to measure the global distribution of aerosols and their effect on the atmospheric heat budget

    NASA Technical Reports Server (NTRS)

    Shipley, S. T.; Joseph, J. H.; Trauger, J. T.; Guetter, P. J.; Eloranta, E. W.; Lawler, J. E.; Wiscombe, W. J.; Odell, A. P.; Roesler, F. L.; Weinman, J. A.

    1975-01-01

    A shuttle-borne lidar system is described, which will provide basic data about aerosol distributions for developing climatological models. Topics discussed include: (1) present knowledge of the physical characteristics of desert aerosols and the absorption characteristics of atmospheric gas, (2) radiative heating computations, and (3) general circulation models. The characteristics of a shuttle-borne radar are presented along with some laboratory studies which identify schemes that permit the implementation of a high spectral resolution lidar system.

  19. A satellite view of aerosols in the climate system

    NASA Technical Reports Server (NTRS)

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

    2002-01-01

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

  20. Toxicity of atmospheric aerosols on marine phytoplankton

    PubMed Central

    Paytan, Adina; Mackey, Katherine R. M.; Chen, Ying; Lima, Ivan D.; Doney, Scott C.; Mahowald, Natalie; Labiosa, Rochelle; Post, Anton F.

    2009-01-01

    Atmospheric aerosol deposition is an important source of nutrients and trace metals to the open ocean that can enhance ocean productivity and carbon sequestration and thus influence atmospheric carbon dioxide concentrations and climate. Using aerosol samples from different back trajectories in incubation experiments with natural communities, we demonstrate that the response of phytoplankton growth to aerosol additions depends on specific components in aerosols and differs across phytoplankton species. Aerosol additions enhanced growth by releasing nitrogen and phosphorus, but not all aerosols stimulated growth. Toxic effects were observed with some aerosols, where the toxicity affected picoeukaryotes and Synechococcus but not Prochlorococcus. We suggest that the toxicity could be due to high copper concentrations in these aerosols and support this by laboratory copper toxicity tests preformed with Synechococcus cultures. However, it is possible that other elements present in the aerosols or unknown synergistic effects between these elements could have also contributed to the toxic effect. Anthropogenic emissions are increasing atmospheric copper deposition sharply, and based on coupled atmosphere–ocean calculations, we show that this deposition can potentially alter patterns of marine primary production and community structure in high aerosol, low chlorophyll areas, particularly in the Bay of Bengal and downwind of South and East Asia. PMID:19273845

  1. Toxicity of atmospheric aerosols on marine phytoplankton

    USGS Publications Warehouse

    Paytan, A.; Mackey, K.R.M.; Chen, Y.; Lima, I.D.; Doney, S.C.; Mahowald, N.; Labiosa, R.; Post, A.F.

    2009-01-01

    Atmospheric aerosol deposition is an important source of nutrients and trace metals to the open ocean that can enhance ocean productivity and carbon sequestration and thus influence atmospheric carbon dioxide concentrations and climate. Using aerosol samples from different back trajectories in incubation experiments with natural communities, we demonstrate that the response of phytoplankton growth to aerosol additions depends on specific components in aerosols and differs across phytoplankton species. Aerosol additions enhanced growth by releasing nitrogen and phosphorus, but not all aerosols stimulated growth. Toxic effects were observed with some aerosols, where the toxicity affected picoeukaryotes and Synechococcus but not Prochlorococcus.We suggest that the toxicity could be due to high copper concentrations in these aerosols and support this by laboratory copper toxicity tests preformed with Synechococcus cultures. However, it is possible that other elements present in the aerosols or unknown synergistic effects between these elements could have also contributed to the toxic effect. Anthropogenic emissions are increasing atmospheric copper deposition sharply, and based on coupled atmosphere-ocean calculations, we show that this deposition can potentially alter patterns of marine primary production and community structure in high aerosol, low chlorophyll areas, particularly in the Bay of Bengal and downwind of South and East Asia.

  2. Toxicity of atmospheric aerosols on marine phytoplankton.

    PubMed

    Paytan, Adina; Mackey, Katherine R M; Chen, Ying; Lima, Ivan D; Doney, Scott C; Mahowald, Natalie; Labiosa, Rochelle; Post, Anton F

    2009-03-24

    Atmospheric aerosol deposition is an important source of nutrients and trace metals to the open ocean that can enhance ocean productivity and carbon sequestration and thus influence atmospheric carbon dioxide concentrations and climate. Using aerosol samples from different back trajectories in incubation experiments with natural communities, we demonstrate that the response of phytoplankton growth to aerosol additions depends on specific components in aerosols and differs across phytoplankton species. Aerosol additions enhanced growth by releasing nitrogen and phosphorus, but not all aerosols stimulated growth. Toxic effects were observed with some aerosols, where the toxicity affected picoeukaryotes and Synechococcus but not Prochlorococcus. We suggest that the toxicity could be due to high copper concentrations in these aerosols and support this by laboratory copper toxicity tests preformed with Synechococcus cultures. However, it is possible that other elements present in the aerosols or unknown synergistic effects between these elements could have also contributed to the toxic effect. Anthropogenic emissions are increasing atmospheric copper deposition sharply, and based on coupled atmosphere-ocean calculations, we show that this deposition can potentially alter patterns of marine primary production and community structure in high aerosol, low chlorophyll areas, particularly in the Bay of Bengal and downwind of South and East Asia. PMID:19273845

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

    SciTech Connect

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

    2008-11-03

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

  4. Identification of characteristic mass spectrometric markers for primary biological aerosol particles and comparison with field data from submicron pristine aerosol particles

    NASA Astrophysics Data System (ADS)

    Freutel, F.; Schneider, J.; Zorn, S. R.; Drewnick, F.; Borrmann, S.; Hoffmann, T.; Martin, S. T.

    2009-04-01

    The contribution of primary biological aerosol (PBA) to the total aerosol particle concentration is estimated to range between 25 and 80%, depending on location and season. Especially in the tropical rain forest it is expected that PBA is a major source of particles in the supermicron range, and is also an important fraction of the submicron aerosol. PBA particles like plant fragments, pollen, spores, fungi, viruses etc. contain chemical compounds as proteins, sugars, amino acids, chlorophyll, and cellular material as cellulose. For this reason we have performed mass spectrometric laboratory measurements (Aerodyne C-ToF and W-ToF AMS, single particle laser ablation instrument SPLAT) on pure submicron aerosol particles containing typical PBA compounds in order to identify typical mass spectral patterns of these compounds and to explain the observed fragmentation patterns on the basis of molecular structures. These laboratory data were compared to submicron particle mass spectra obtained during AMAZE-08 (Amazonian Aerosol CharacteriZation Experiment, Brazil, February/March 2008). The results indicate that characteristic m/z ratios for carbohydrates (e.g., glucose, saccharose, levoglucosan, mannitol) can be identified, for example m/z = 60(C2H4O2+) or m/z = 61(C2H5O2+). Certain characteristic peaks for amino acids were also identified in the laboratory experiments. In the field data from AMAZE-08, these characteristic peaks for carbohydrates and amino acids were found, and their contribution to the total organic mass was estimated to about 5%. Fragment ions from peptides and small proteins were also identified in laboratory experiments. Larger proteins, however, seem to become oxidized to CO2+ to a large extend in the vaporizing process of the AMS. Thus, detection of proteins in atmospheric aerosol particles with the AMS appears to be difficult.

  5. A global aerosol classification algorithm incorporating multiple satellite data sets of aerosol and trace gas abundances

    NASA Astrophysics Data System (ADS)

    Penning de Vries, M. J. M.; Beirle, S.; Hörmann, C.; Kaiser, J. W.; Stammes, P.; Tilstra, L. G.; Tuinder, O. N. E.; Wagner, T.

    2015-09-01

    Detecting the optical properties of aerosols using passive satellite-borne measurements alone is a difficult task due to the broadband effect of aerosols on the measured spectra and the influences of surface and cloud reflection. We present another approach to determine aerosol type, namely by studying the relationship of aerosol optical depth (AOD) with trace gas abundance, aerosol absorption, and mean aerosol size. Our new Global Aerosol Classification Algorithm, GACA, examines relationships between aerosol properties (AOD and extinction Ångström exponent from the Moderate Resolution Imaging Spectroradiometer (MODIS), UV Aerosol Index from the second Global Ozone Monitoring Experiment, GOME-2) and trace gas column densities (NO2, HCHO, SO2 from GOME-2, and CO from MOPITT, the Measurements of Pollution in the Troposphere instrument) on a monthly mean basis. First, aerosol types are separated based on size (Ångström exponent) and absorption (UV Aerosol Index), then the dominating sources are identified based on mean trace gas columns and their correlation with AOD. In this way, global maps of dominant aerosol type and main source type are constructed for each season and compared with maps of aerosol composition from the global MACC (Monitoring Atmospheric Composition and Climate) model. Although GACA cannot correctly characterize transported or mixed aerosols, GACA and MACC show good agreement regarding the global seasonal cycle, particularly for urban/industrial aerosols. The seasonal cycles of both aerosol type and source are also studied in more detail for selected 5° × 5° regions. Again, good agreement between GACA and MACC is found for all regions, but some systematic differences become apparent: the variability of aerosol composition (yearly and/or seasonal) is often not well captured by MACC, the amount of mineral dust outside of the dust belt appears to be overestimated, and the abundance of secondary organic aerosols is underestimated in comparison

  6. Optimal Delivery of Aerosols to Infants During Mechanical Ventilation

    PubMed Central

    Azimi, Mandana; Hindle, Michael

    2014-01-01

    Abstract Purpose: The objective of this study was to determine optimal aerosol delivery conditions for a full-term (3.6 kg) infant receiving invasive mechanical ventilation by evaluating the effects of aerosol particle size, a new wye connector, and timing of aerosol delivery. Methods: In vitro experiments used a vibrating mesh nebulizer and evaluated drug deposition fraction and emitted dose through ventilation circuits containing either a commercial (CM) or new streamlined (SL) wye connector and 3-mm endotracheal tube (ETT) for aerosols with mass median aerodynamic diameters of 880 nm, 1.78 μm, and 4.9 μm. The aerosol was released into the circuit either over the full inhalation cycle (T1 delivery) or over the first half of inhalation (T2 delivery). Validated computational fluid dynamics (CFD) simulations and whole-lung model predictions were used to assess lung deposition and exhaled dose during cyclic ventilation. Results: In vitro experiments at a steady-state tracheal flow rate of 5 L/min resulted in 80–90% transmission of the 880-nm and 1.78-μm aerosols from the ETT. Based on CFD simulations with cyclic ventilation, the SL wye design reduced depositional losses in the wye by a factor of approximately 2–4 and improved lung delivery efficiencies by a factor of approximately 2 compared with the CM device. Delivery of the aerosol over the first half of the inspiratory cycle (T2) reduced exhaled dose from the ventilation circuit by a factor of 4 compared with T1 delivery. Optimal lung deposition was achieved with the SL wye connector and T2 delivery, resulting in 45% and 60% lung deposition for optimal polydisperse (∼1.78 μm) and monodisperse (∼2.5 μm) particle sizes, respectively. Conclusions: Optimization of selected factors and use of a new SL wye connector can substantially increase the lung delivery efficiency of medical aerosols to infants from current values of <1–10% to a range of 45–60%. PMID:24299500

  7. Characteristics of aerosolized ice forming marine biogenic particles

    NASA Astrophysics Data System (ADS)

    Alpert, Peter A.

    Ice particles are ubiquitous in the atmosphere existing as the sole constituents of glaciated cirrus clouds or coexisting with supercooled liquid droplets in mixed-phase clouds. Aerosol particles serving as heterogeneous ice nuclei for ice crystal formation impact the global radiative balance by modification of cloud radiative properties, and thus climate. Atmospheric ice formation is not a well understood process and represents great uncertainty for climate prediction. The oceans which cover the majority of the earth's surface host nearly half the total global primary productivity and contribute to the greatest aerosol production by mass. However, the effect of biological activity on particle aerosolization, particle composition, and ice nucleation is not well established. This dissertation investigates the link between marine biological activity, aerosol particle production, physical/chemical particle characteristics, and ice nucleation under controlled laboratory conditions. Dry and humidified aerosol size distributions of particles from bursting bubbles generated by plunging water jets and aeration through frits in a seawater mesocosm containing bacteria and/or phytoplankton cultures, were measured as a function of biological activity. Total particle production significantly increases primarily due to enhanced aerosolization of particles ≤100 nm in diameter attributable to the presence and growth of phytoplankton. Furthermore, hygroscopicity measurements indicate primary organic material associated with the sea salt particles, providing additional evidence for the importance of marine biological activity for ocean derived aerosol composition. Ice nucleation experiments show that these organic rich particles nucleate ice efficiently in the immersion and deposition modes, which underscores their importance in mixed-phase and cirrus cloud formation processes. In separate ice nucleation experiments employing pure cultures of Thalassiosira pseudonana, Nannochloris

  8. Influence of aerosols on atmospheric variables in the HARMONIE model

    NASA Astrophysics Data System (ADS)

    Palamarchuk, Iuliia; Ivanov, Sergiy; Ruban, Igor; Pavlova, Hanna

    2016-03-01

    The mesoscale HARMONIE model is used to investigate the potential influence of aerosols on weather forecasts, and in particular, on precipitation. The study considers three numerical experiments over the Atlantic-Europe-Northern Africa region during 11-16 August 2010 with the following configurations: (a) no aerosols, (b) only the sea aerosols, and (c) the four types of the aerosols: sea, land, organic, and dust aerosols. The spatio-temporal analysis of forecast differences highlights the impact of aerosols on the prediction of main meteorological variables such as air temperature, humidity, precipitation, and cloud cover as well as their vertical profiles. The variations occur through changes in radiation fluxes and microphysics properties. The sensitivity experiments with the inclusion of climatological aerosol concentrations demonstrate the importance of aerosol effects on weather prediction.

  9. Efficient Nose-to-Lung (N2L) Aerosol Delivery with a Dry Powder Inhaler

    PubMed Central

    Golshahi, Laleh; Behara, Srinivas R.B.; Tian, Geng; Farkas, Dale R.; Hindle, Michael

    2015-01-01

    Abstract Purpose: Delivering aerosols to the lungs through the nasal route has a number of advantages, but its use has been limited by high depositional loss in the extrathoracic airways. The objective of this study was to evaluate the nose-to-lung (N2L) delivery of excipient enhanced growth (EEG) formulation aerosols generated with a new inline dry powder inhaler (DPI). The device was also adapted to enable aerosol delivery to a patient simultaneously receiving respiratory support from high flow nasal cannula (HFNC) therapy. Methods: The inhaler delivered the antibiotic ciprofloxacin, which was formulated as submicrometer combination particles containing a hygroscopic excipient prepared by spray-drying. Nose-to-lung delivery was assessed using in vitro and computational fluid dynamics (CFD) methods in an airway model that continued through the upper tracheobronchial region. Results: The best performing device contained a 2.3 mm flow control orifice and a 3D rod array with a 3-4-3 rod pattern. Based on in vitro experiments, the emitted dose from the streamlined nasal cannula had a fine particle fraction <5 μm of 95.9% and mass median aerodynamic diameter of 1.4 μm, which was considered ideal for nose-to-lung EEG delivery. With the 2.3-343 device, condensational growth in the airways increased the aerosol size to 2.5–2.7 μm and extrathoracic deposition was <10%. CFD results closely matched the in vitro experiments and predicted that nasal deposition was <2%. Conclusions: The developed DPI produced high efficiency aerosolization with significant size increase of the aerosol within the airways that can be used to enable nose-to-lung delivery and aerosol administration during HFNC therapy. PMID:25192072

  10. Satellite Remote Sensing: Aerosol Measurements

    NASA Technical Reports Server (NTRS)

    Kahn, Ralph A.

    2013-01-01

    Aerosols are solid or liquid particles suspended in the air, and those observed by satellite remote sensing are typically between about 0.05 and 10 microns in size. (Note that in traditional aerosol science, the term "aerosol" refers to both the particles and the medium in which they reside, whereas for remote sensing, the term commonly refers to the particles only. In this article, we adopt the remote-sensing definition.) They originate from a great diversity of sources, such as wildfires, volcanoes, soils and desert sands, breaking waves, natural biological activity, agricultural burning, cement production, and fossil fuel combustion. They typically remain in the atmosphere from several days to a week or more, and some travel great distances before returning to Earth's surface via gravitational settling or washout by precipitation. Many aerosol sources exhibit strong seasonal variability, and most experience inter-annual fluctuations. As such, the frequent, global coverage that space-based aerosol remote-sensing instruments can provide is making increasingly important contributions to regional and larger-scale aerosol studies.

  11. SAGE II aerosol data validation based on retrieved aerosol model size distribution from SAGE II aerosol measurements.

    PubMed

    Wang, P H; McCormick, M P; McMaster, L R; Chu, W P; Swissler, T J; Osborn, M T; Russell, P B; Oberbeck, V R; Livingston, J; Rosen, J M; Hofmann, D J; Grams, G W; Fuller, W H; Yue, G K

    1989-06-20

    This paper describes an investigation of the comprehensive aerosol correlative measurement experiments conducted between November 1984 and July 1986 for satellite measurement program of the Stratospheric Aerosol and Gas Experiment (SAGE II). The correlative sensors involved in the experiments consist of the NASA Ames Research Center impactor/laser probe, the University of Wyoming dustsonde, and the NASA Langley Research Center airborne 14-inch (36 cm) lidar system. The approach of the analysis is to compare the primary aerosol quantities measured by the ground-based instruments with the calculated ones based on the aerosol size distributions retrieved from the SAGE II aerosol extinction measurements. The analysis shows that the aerosol size distributions derived from the SAGE II observations agree qualitatively with the in situ measurements made by the impactor/laser probe. The SAGE II-derived vertical distributions of the ratio N0.15/N0.25 (where Nr is the cumulative aerosol concentration for particle radii greater than r, in micrometers) and the aerosol backscatter profiles at 0.532- and 0.6943-micrometer lidar wavelengths are shown to agree with the dustsonde and the 14-inch (36-cm) lidar observations, with the differences being within the respective uncertainties of the SAGE II and the other instruments. PMID:11539801

  12. [The institutional promotion of good practices in the operational management of health and safety: the experience of Italy Crown Aerosols on the monitoring of behavior].

    PubMed

    de Merich, D; Pellicci, M; Serignoli, R

    2010-01-01

    Within the intelligence support and training to small and medium-sized enterprises (SMEs) and promoting a culture of health and safety at work, ISPESL is engaged on two fundamental pillars of activity: Consolidation of the national surveillance system of injuries through the promotion of methods and tools for the reconstruction of the dynamics incidental identification of causal determinants, with the aim of improving the capabilities of risk assessment of systems to prevent corporate. The promotion of good working practices, as Focal Point of the European Health and Safety at Work in Bilbao, the goal is to support prevention activities by providing business application examples of measures for improvement (technical, organizational, procedural) made in the proposing firms and validated by a technical appraisal conducted by ISPESL. Among the methodologies and tools that can be made available to companies in the operational management of health and safety in work activities, the approach to analyze and evaluate the behavior implemented by all persons within the company (managers, employees, workers) is a the most innovative preventive strategies that can be implemented to correct any improper practices behavioral wrongly tolerated in everyday work practice. The experience of Crown Aerosol Italy, the program "STOP TO ACCIDENTS, 2009 Best Practices award in the competition on the theme" Risk Assessment ", aims to demonstrate how the application of a method for monitoring behavior at work, shared in its planning with all those business, has not only reached but would assist the organization has developed at an individual level greater awareness and sense of responsibility also to their colleagues, by promoting good working practices. PMID:20518217

  13. Toward Creating A Global Retrospective Climatology of Aerosol Properties

    NASA Technical Reports Server (NTRS)

    Curran, Robert J.; Mishchenko, Michael I.; Hansen, James E. (Technical Monitor)

    2000-01-01

    Tropospheric aerosols are thought to cause a significant direct and indirect climate forcing, but the magnitude of this forcing remains highly uncertain because of poor knowledge of global aerosol characteristics and their temporal changes. The standard long-term global product, the one-channel Advanced Very-High-Resolution Radiometer (AVHRR) aerosol optical thickness over the ocean, relies on a single predefined aerosol model and can be inaccurate in many cases. Furthermore, it provides no information on aerosol column number density, thus making it impossible to estimate the indirect aerosol effect on climate. Total Ozone Mapping Spectrometer (TOMS) data can be used to detect absorbing aerosols over land, but are insensitive to aerosols located below one kilometer. It is thus clear that innovative approaches must be employed in order to extract a more quantitative and accurate aerosol climatology from available satellite and other measurements, thus enabling more reliable estimates of the direct and indirect aerosol forcings. The Global Aerosol Climatology Project (GACP) was established in 1998 as part of the Global Energy and Water Cycle Experiment (GEWEX). Its main objective is to analyze satellite radiance measurements and field observations to infer the global distribution of aerosols, their properties, and their seasonal and interannual variations. The overall goal is to develop advanced global aerosol climatologies for the period of satellite data and to make the aerosol climatologies broadly available through the GACP web site.

  14. Genesis of elevated aerosol loading over the Indian region

    NASA Astrophysics Data System (ADS)

    Prijith, S. S.; Rao, P. V. N.; Mohan, Mannil

    2016-05-01

    Elevated aerosols assume importance as the diabatic heating due to aerosol absorption is more intense at higher altitudes where the atmosphere becomes thinner. Indian region, especially its central and northern latitudes, experiences significant loading of elevated aerosols during pre-monsoon and summer months. Genesis of elevated aerosol loading over Indian region is investigated in the present study, using multi-year satellite observations from Cloud Aerosol Lidar with Orthogonal Polarization (CALIOP) and Moderate Resolution Imaging Spectroradiometer (MODIS) along with reanalysis winds from MERRA. Central India is observed to have prominent aerosols loading at higher altitudes during pre-monsoon season, whereas it is during summer months over north-west India. Further analysis reveals that the elevated aerosols over Indian region in pre-monsoon and summer months are significantly contributed by transported mineral dust from the arid continental regions at west. In addition to the mineral dust advection, aerosols at higher altitudes over Indian region are enriched by strong convection and associated vertical transport of surface level aerosols. Vertical transport of aerosols observed over Indian region during pre-monsoon and summer months is aided by intense convergence at the surface level and divergence at the upper level. Moreover, aerosol source/sink strength estimated using aerosol flux continuity equation show significant aerosol production over central India during pre-monsoon. Strong vertical transport prevails during pre-monsoon uplifts the locally produced aerosols, with considerable anthropogenic fraction, to higher altitudes where their impacts would be more intense.

  15. SECONDARY ORGANIC AEROSOL FORMATION FROM THE OXIDATION OF AROMATIC HYDROCARBONS IN THE PRESENCE OF DRY SUBMICRON AMMONIUM SULFATE AEROSOL

    EPA Science Inventory

    A laboratory study was conducted to examine formation of secondary organic aerosols. A smog chamber system was developed for studying gas-aerosol interactions in a dynamic flow reactor. These experiments were conducted to investigate the fate of gas and aerosol phase compounds ...

  16. Experimental Assessment of Collection Efficiency of Submicron Aerosol Particles by Cloud Droplets

    NASA Astrophysics Data System (ADS)

    Huang, Y.; Oo, K.; Brown, M. D.; Dhaniyala, S.; Cziczo, D. J.

    2012-12-01

    An experimental setup has been constructed to measure the collection efficiency of submicron aerosol particles by cloud droplets. The collection efficiency study is a prelude to studying contact nucleation, which is a potentially important ice nucleation mode that is not well-understood. This laboratory setup is a step closer to experimentally assessing the importance of contact nucleation. Water droplets with 20 micron diameter and submicron aerosol particles are brought into contact in an injector situated inside a chilled glass flow tube. The water droplets that collect aerosol particles are allowed to pass through a counterflow virtual impactor (CVI), which accepts large droplets and rejects aerosol particles that have not coagulated with the water droplets. The collected droplets are sent into the Particle Analysis by Laser Mass Spectrometry (PALMS) instrument which performs in situ chemical analysis of a single particle. The number of aerosol particles collected by the single water droplet is quantified by calibrating the PALMS with known concentrations of aerosol particles. The water droplets contain a known amount of ammonium sulfate for identification purpose in the mass spectrometry. Preliminary results from the experiment will be discussed and compared with previous theoretical and experimental studies.

  17. New Photosensitized Processes at Aerosol and Ocean Surfaces

    NASA Astrophysics Data System (ADS)

    Rossignol, S.; Aregahegn, K. Z.; Ciuraru, R.; Bernard, F.; Tinel, L.; Fine, L.; George, C.

    2014-12-01

    From a few years now, there is a growing body of evidence that photoinduced processes could be of great importance for the tropospheric chemistry. Here, we would like to present two additional outcomes of this new area of research, firstly the photosensitized direct VOC uptake by aerosols and, secondly, the photoinduced chemical formation of unsaturated VOC from marine microlayer proxy. It was recently shown that the chemistry of glyoxal toward ammonium ions into droplets and wet aerosols leads to the formation of light-absorbing compounds. Among them, we found that imidazole-2-carboxaldehyde (IC) acts as a photosensitizer and is able to initiate the growth of organic aerosols via the uptake of VOC, such as limonene. Given its potential importance, the mechanism of this photoinduced uptake was investigated thanks to aerosol flow tube experiments and UPLC-ESI-HRMS analysis. Results reveal hydrogen abstraction on the VOC molecule by the triplet state of IC leading to the VOC oxidation without any traditional oxidant. As well as aerosol, the sea-surface microlayer, known to be enriched in light-absorbing organics, is largely impacted by photochemical processes. Recent studies have pointed out for example the role of photosentitized processes in the loss of NO2 and ozone at water surfaces containing photoactive compounds such as chlorophyll. In order to go further, we worked from sea-surface microlayer proxy containing humic acids as photoactive material and organic acids as surfactants. Beside oxidation processes, we monitored by high resolution PTR-MS the release in the gas phase of unsaturated compounds, including C5 dienes (isoprene ?). A strong correlation between the measured surface tension and the C5 diene concentration in the gas phase was evidenced, clearly pointing toward an interfacial process. This contribution will highlight the similarities between both systems and will attempt to present a general chemical scheme for photosensitized chemistry at

  18. Global Aerosol Optical Models and Lookup Tables for the New MODIS Aerosol Retrieval over Land

    NASA Technical Reports Server (NTRS)

    Levy, Robert C.; Remer, Loraine A.; Dubovik, Oleg

    2007-01-01

    Since 2000, MODIS has been deriving aerosol properties over land from MODIS observed spectral reflectance, by matching the observed reflectance with that simulated for selected aerosol optical models, aerosol loadings, wavelengths and geometrical conditions (that are contained in a lookup table or 'LUT'). Validation exercises have showed that MODIS tends to under-predict aerosol optical depth (tau) in cases of large tau (tau greater than 1.0), signaling errors in the assumed aerosol optical properties. Using the climatology of almucantur retrievals from the hundreds of global AERONET sunphotometer sites, we found that three spherical-derived models (describing fine-sized dominated aerosol), and one spheroid-derived model (describing coarse-sized dominated aerosol, presumably dust) generally described the range of observed global aerosol properties. The fine dominated models were separated mainly by their single scattering albedo (omega(sub 0)), ranging from non-absorbing aerosol (omega(sub 0) approx. 0.95) in developed urban/industrial regions, to neutrally absorbing aerosol (omega(sub 0) approx.90) in forest fire burning and developing industrial regions, to absorbing aerosol (omega(sub 0) approx. 0.85) in regions of savanna/grassland burning. We determined the dominant model type in each region and season, to create a 1 deg. x 1 deg. grid of assumed aerosol type. We used vector radiative transfer code to create a new LUT, simulating the four aerosol models, in four MODIS channels. Independent AERONET observations of spectral tau agree with the new models, indicating that the new models are suitable for use by the MODIS aerosol retrieval.

  19. Photochemistry of Model Organic Aerosol Systems

    NASA Astrophysics Data System (ADS)

    Mang, S. A.; Bateman, A. P.; Dailo, M.; Do, T.; Nizkorodov, S. A.; Pan, X.; Underwood, J. S.; Walser, M. L.

    2007-05-01

    Up to 90 percent of urban aerosol particles have been shown to contain organic molecules. Reactions of these particles with atmospheric oxidants and/or sunlight result in large changes in their composition, toxicity, and ability to act as cloud condensation nuclei. For this reason, chemistry of model organic aerosol particles initiated by oxidation and direct photolysis is of great interest to atmospheric, climate, and health scientists. Most studies in this area have focused on identifying the products of oxidation of the organic aerosols, while the products of direct photolysis of the resulting molecules remaining in the aerosol particle have been left mostly unexplored. We have explored direct photolytic processes occurring in selected organic aerosol systems using infrared cavity ringdown spectroscopy to identify small gas phase products of photolysis, and mass-spectrometric and photometric techniques to study the condensed phase products. The first model system was secondary organic aerosol formed from the oxidation of several monoterpenes by ozone in the presence and absence of NOx, under different humidities. The second system modeled after oxidatively aged primary organic aerosol particles was a thin film of either alkanes or saturated fatty acids oxidized in several different ways, with the oxidation initiated by ozone, chlorine atom, or OH. In every case, the general conclusion was that the photochemical processing of model organic aerosols is significant. Such direct photolysis processes are believed to age organic aerosol particles on time scales that are short compared to the particles' atmospheric lifetimes.

  20. A study of small systems containing H and O atoms using nonlocal functionals: Comparison with ab initio and experiment

    SciTech Connect

    Seminario, J.M.

    1994-12-31

    Structures and energies have been calculated for HO, H{sub 2}O, O{sub 2}, HO{sub 2}, H{sub 2}O{sub 2}, and O{sub 3} molecules using the nonlocal functionals PW 86, PW 91, B-P86, and B-LYP with the goal of obtaining their atomization energies. Results were compared with those form highly correlated methods and experiment. It was found that all nonlocal functionals perform similarly to or better than correlated methods MP4 and QCI (using relatively equivalent basis sets). All nonlocal energies were self-consistently calculated using the optimized geometries for each functional. None of the results contain any empirical correction except those inherent to some of the functionals. Increasing the size of the basis set when using the nonlocal functionals does not lead to any significant improvement of the energies and surprisingly it worsens the results for one of the functionals.

  1. Swelling under irradiation of MgO pellets containing americium oxide: The ECRIX-H irradiation experiment

    NASA Astrophysics Data System (ADS)

    Lamontagne, J.; Béjaoui, S.; Hanifi, K.; Valot, Ch.; Loubet, L.

    2011-06-01

    The ECRIX-H irradiation experiment studied the behaviour of pellets containing americium dispersed in MgO. The purpose of the irradiation was to demonstrate the capacity of magnesia to provide an efficient support matrix. After fabrication, the sintered pellets contained 16.65 wt.% of Am microdispersed in the inert matrix. The ECRIX-H pellets were irradiated under a locally moderated neutron flux in the Phénix sodium-cooled fast reactor (SFR) for 318 Effective Full Power Days (EFPD). Post-test calculations indicated that the fission and transmutation rates of americium at the maximum flux plane reached 33.9% and 92.6% respectively at the end of the irradiation phase. The results of the post-irradiation examinations - both non-destructive and destructive - are discussed in this paper. These results indicate a satisfactory behaviour of the MgO matrix. Particularly, a moderate swelling occurs in the pellets under irradiation even with significant quantities of helium generated and at high transmutation rate.

  2. Aerosol concentration and size distribution measured below, in, and above cloud from the DOE G-1 during VOCALS-REx

    SciTech Connect

    Kleinman L. I.; Daum, P. H.; Lee, Y.-N.; Lewis, E. R.; Sedlacek III, A. J.; Senum, G. I.; Springston, S. R.; Wang, J.; Hubbe, J.; Jayne, J.; Min, Q.; Yum, S. S.; Allen, G.

    2012-01-04

    During the VOCALS Regional Experiment, the DOE G-1 aircraft was used to sample a varying aerosol environment pertinent to properties of stratocumulus clouds over a longitude band extending 800 km west from the Chilean coast at Arica. Trace gas and aerosol measurements are presented as a function of longitude, altitude, and dew point in this study. Spatial distributions are consistent with an upper atmospheric source for O{sub 3} and South American coastal sources for marine boundary layer (MBL) CO and aerosol, most of which is acidic sulfate. Pollutant layers in the free troposphere (FT) can be a result of emissions to the north in Peru or long range transport from the west. At a given altitude in the FT (up to 3 km), dew point varies by 40 C with dry air descending from the upper atmospheric and moist air having a boundary layer (BL) contribution. Ascent of BL air to a cold high altitude results in the condensation and precipitation removal of all but a few percent of BL water along with aerosol that served as CCN. Thus, aerosol volume decreases with dew point in the FT. Aerosol size spectra have a bimodal structure in the MBL and an intermediate diameter unimodal distribution in the FT. Comparing cloud droplet number concentration (CDNC) and pre-cloud aerosol (D{sub p} > 100 nm) gives a linear relation up to a number concentration of {approx}150 cm{sup -3}, followed by a less than proportional increase in CDNC at higher aerosol number concentration. A number balance between below cloud aerosol and cloud droplets indicates that {approx}25 % of aerosol with D{sub p} > 100 nm are interstitial (not activated). A direct comparison of pre-cloud and in-cloud aerosol yields a higher estimate. Artifacts in the measurement of interstitial aerosol due to droplet shatter and evaporation are discussed. Within each of 102 constant altitude cloud transects, CDNC and interstitial aerosol were anti-correlated. An examination of one cloud as a case study shows that the

  3. Aerosolization, Chemical Characterization, Hygroscopicity and Ice Formation of Marine Biogenic Particles

    NASA Astrophysics Data System (ADS)

    Alpert, P. A.; Radway, J.; Kilthau, W.; Bothe, D.; Knopf, D. A.; Aller, J. Y.

    2013-12-01

    The oceans cover the majority of the earth's surface, host nearly half the total global primary productivity and are a major source of atmospheric aerosol particles. However, effects of biological activity on sea spray generation and composition, and subsequent cloud formation are not well understood. Our goal is to elucidate these effects which will be particularly important over nutrient rich seas, where microorganisms can reach concentrations of 10^9 per mL and along with transparent exopolymer particles (TEP) can become aerosolized. Here we report the results of mesocosm experiments in which bubbles were generated by two methods, either recirculating impinging water jets or glass frits, in natural or artificial seawater containing bacteria and unialgal cultures of three representative phytoplankton species, Thalassiosira pseudonana, Emiliania huxleyi, and Nannochloris atomus. Over time we followed the size distribution of aerosolized particles as well as their hygroscopicity, heterogeneous ice nucleation potential, and individual physical-chemical characteristics. Numbers of cells and the mass of dissolved and particulate organic carbon (DOC, POC), TEP (which includes polysaccharide-containing microgels and nanogels >0.4 μm in diameter) were determined in the bulk water, the surface microlayer, and aerosolized material. Aerosolized particles were also impacted onto substrates for ice nucleation and water uptake experiments, elemental analysis using computer controlled scanning electron microscopy and energy dispersive analysis of X-rays (CCSEM/EDX), and determination of carbon bonding with scanning transmission X-ray microscopy and near-edge X-ray absorption fine structure spectroscopy (STXM/NEXAFS). Regardless of bubble generation method, the overall concentration of aerosol particles, TEP, POC and DOC increased as concentrations of bacterial and phytoplankton cells increased, stabilized, and subsequently declined. Particles <100 nm generated by means of jets

  4. Understanding the impact of saharan dust aerosols on tropical cyclones

    NASA Astrophysics Data System (ADS)

    Naeger, Aaron

    Genesis of Tropical Cyclones (TCs) in the main development region for Atlantic hurricanes is tied to convection initiated by African easterly waves (AEWs) during Northern hemisphere summer and fall seasons. The main development region is also impacted by dust aerosols transported from the Sahara. It has been hypothesized that dust aerosols can modulate the development of TCs through aerosol-radiation and aerosol-cloud interaction processes. In this study, we investigate the impact of dust aerosols on TC development using the Weather Research and Forecasting model coupled with chemistry (WRF-Chem). We first develop a technique to constrain the WRF-Chem model with a realistic three-dimensional spatial distribution of dust aerosols. The horizontal distribution of dust is specified using the Moderate Resolution Imaging Spectroradiometer (MODIS) derived aerosol products and output from the Goddard Chemistry Aerosol Radiation and Transport (GOCART) model. The vertical distribution of dust is constrained using the Cloud Aerosol Lidar and Infrared Pathfinder Satellite Observations (CALIPSO). We validate our technique through in situ aircraft measurements where both showed aerosol number concentrations from 20-30 cm-3 in the atmosphere for Saharan dust moving over the eastern Atlantic Ocean. Then, we use the satellite data constraint technique to nudge the WRF-Chem aerosol fields throughout the simulation of TC Florence developing over the eastern Atlantic Ocean during September 2006. Three different experiments are conducted where the aerosol-radiation and aerosol-cloud interaction processes are either activated or deactivated in the model while all other model options are identical between the experiments. By comparing the model experiment results, the impact of the aerosol interaction processes on TC development can be understood. The results indicate that dust aerosols can delay or prevent the development of a TC as the minimum sea level pressure of TC Florence was 13 h

  5. Measurements and Modeling of Aerosol Absorption and Single Scattering Albedo at Ambient Relative Hum

    NASA Technical Reports Server (NTRS)

    Redemann, J.; Russell, P. B.; Hamill, P.

    2000-01-01

    Uncertainties in the aerosol single scattering albedo have been identified to be an important source of errors in current large-scale model estimates of the direct aerosol radiative forcing of climate. A number of investigators have obtained estimates of the single scattering albedo from a variety of remote sensing and in situ measurements during aerosol field experiments. During the Tropospheric Aerosol Radiative Forcing Observational Experiment (TARFOX, 1996) for example, estimates of the aerosol single scattering albedo were obtained (1) as a best-fit parameter in comparing radiative flux changes measured by airborne pyranometer to those computed from independently measured aerosol properties; (2) from estimates of the aerosol complex index of refraction derived using a combination of airborne sunphotometer, lidar backscatter and in situ size distribution measurements; and (3) from airborne measurements of aerosol scattering and absorption using nephelometers and absorption photometers. In this paper, we briefly compare the results of the latter two methods for two TARFOX case studies, since those techniques provide height-resolved information about the aerosol single scattering albedo. Estimates of the aerosol single scattering albedo from nephelometer and absorption photometer measurements require knowledge of the scattering and absorption humidification (i.e., the increase in these properties in response to an increase in ambient relative humidity), since both measurements are usually carried out at a relative humidity different from the ambient atmosphere. In principle, the scattering humidification factor can be measured, but there is currently no technique widely available to measure the absorption of an aerosol sample as a function of relative humidity. Frequently, for lack of better knowledge, the absorption humidification is assumed to be unity (meaning that there is no change in aerosol absorption due to an increase in ambient relative humidity). This

  6. Aldol Condensation Products and Polyacetals in Organic Films Formed from Reactions of Propanal in Sulfuric Acid at Upper Troposphere/Lower Stratosphere (UT/LS) Aerosol Acidities

    NASA Astrophysics Data System (ADS)

    Bui, J. V. H.; Perez-Montano, S.; Li, E. S. W.; Nelson, T. E.; Ha, K. T.; Leong, L.; Iraci, L. T.; Van Wyngarden, A. L.

    2015-12-01

    Aerosols in the upper troposphere and lower stratosphere (UT/LS) consist mostly of concentrated sulfuric acid (40-80 wt. %) which is highly reflective towards UV and visible radiation. However, airborne measurements have shown that these particles may also contain a significant amount of organic material. Experiments combining organics (propanal, glyoxal and/or methylglyoxal) with sulfuric acid at concentrations typical of UT/LS aerosols produced highly colored surface films (and solutions) t