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Sample records for aerosol mixing ratio

  1. New Examination of the Traditional Raman Lidar Technique II: Temperature Dependence Aerosol Scattering Ratio and Water Vapor Mixing Ratio Equations

    NASA Technical Reports Server (NTRS)

    Whiteman, David N.; Abshire, James B. (Technical Monitor)

    2002-01-01

    In a companion paper, the temperature dependence of Raman scattering and its influence on the Raman water vapor signal and the lidar equations was examined. New forms of the lidar equation were developed to account for this temperature sensitivity. Here we use those results to derive the temperature dependent forms of the equations for the aerosol scattering ratio, aerosol backscatter coefficient, extinction to backscatter ratio and water vapor mixing ratio. Pertinent analysis examples are presented to illustrate each calculation.

  2. Estimated SAGE II ozone mixing ratios in early 1993 and comparisons with Stratospheric Photochemistry, Aerosols and Dynamic Expedition measurements

    NASA Technical Reports Server (NTRS)

    Yue, G. K.; Veiga, R. E.; Poole, L. R.; Zawodny, J. M.; Proffitt, M. H.

    1994-01-01

    An empirical time-series model for estimating ozone mixing ratios based on Stratospheric Aerosols and Gas Experiment II (SAGE II) monthly mean ozone data for the period October 1984 through June 1991 has been developed. The modeling results for ozone mixing ratios in the 10- to 30- km region in early months of 1993 are presented. In situ ozone profiles obtained by a dual-beam UV-absorption ozone photometer during the Stratospheric Photochemistry, Aerosols and Dynamics Expedition (SPADE) campaign, May 1-14, 1993, are compared with the model results. With the exception of two profiles at altitudes below 16 km, ozone mixing ratios derived by the model and measured by the ozone photometer are in relatively good agreement within their individual uncertainties. The identified discrepancies in the two profiles are discussed.

  3. Seasonal variations in Titan's stratosphere observed with Cassini/CIRS: temperature, trace molecular gas and aerosol mixing ratio profiles

    NASA Astrophysics Data System (ADS)

    Vinatier, S.; Bézard, B.; Lebonnois, S.; Teanby, N. A.; Rannou, P.; Anderson, C. M.; Achterberg, R. K.

    2013-12-01

    Titan's northern spring equinox occurred in August 2009. General Circulation Models predict strong modifications of the global circulation in this period, with formation of two circulation cells instead of the pole-to-pole cell that occurred during northern winter. This winter single cell, which had its descending branch at the north pole, was at the origin of the enrichment of molecular abundances and high stratopause temperatures observed by Cassini/CIRS at high northern latitudes. The predicted dynamical seasonal variations after the equinox have strong impact on the spatial distributions of trace gas, temperature and aerosol abundances. We will present here an analysis of CIRS limb-geometry datasets acquired between 2009 and 2013 that we used to monitor the seasonal evolution of the vertical profiles of temperature, molecular (C2H2, C2H6, HCN, ...) and aerosol abundances.

  4. Seasonal Variations in Titan's Stratosphere Observed with Cassini/CIRS: Temperature, Trace Molecular Gas and Aerosol Mixing Ratio Profiles

    NASA Technical Reports Server (NTRS)

    Vinatier, S.; Bezard, B.; Anderson, C. M.; Coustenis, A.; Teanby, N.

    2012-01-01

    Titan's northern spring equinox occurred in August 2009. General Circulation Models (e.g. Lebonnois et al., 2012) predict strong modifications of the global circulation in this period, with formation of two circulation cells instead of the pole-to-pole cell that occurred during northern winter. This winter single cell, which had its descending branch at the north pole, was at the origin of the enrichment of molecular abundances and high stratopause temperatures observed by Cassini/CIRS at high northern latitudes (e.g. Achterberg et al., 2011, Coustenis et al., 2010, Teanby et al., 2008, Vinatier et al., 2010). The predicted dynamical seasonal variations after the equinox have strong impact on the spatial distributions of trace gas, temperature and aerosol abundances. We will present here an analysis of CIRS limb-geometry datasets acquired in 2010 and 2011 that we used to monitor the seasonal evolution of the vertical profiles of temperature, molecular (C2H2, C2H6, HCN, ..) and aerosol abundances.

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

    PubMed

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

    2001-01-01

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

  6. Shaken, not Stirred: Mixing Organic Aerosol

    NASA Astrophysics Data System (ADS)

    Donahue, N. M.; Robinson, E.; Trump, E. R.; Saleh, R.

    2013-12-01

    For organic vapors to condense onto or into existing particles in the atmosphere, the compounds must have a positive thermodynamic driving force. Their activity (saturation ratio) in the gas phase must exceed their activity (modified mole fraction) at the particle surface. Organic-aerosol production rates are generally quite small -- a few μg m-3 per hour at most -- and thus gas-phase saturation ratios are correspondingly small. Most experiments are conducted with far higher production rates and thus far higher saturation ratios. Consequently, experiments may or may not constrain whether organics coat particles in the real world. In addition, surface activity is often assumed to equal bulk activity for most species, meaning that particles are well mixed. However, if particles are viscous and coating rates high, diffusion through the bulk of even 100 nm particles may be slow. Again, matching experimental timescales to real-world timescales is important. Here we describe organic particle mixing experiments in which two organic particle populations are prepared separately and then intermingled by transferring the contents of one preparation chamber into another. Constituents of one population are isotopically labeled, making the mass spectra of the two particle types completely orthogonal. Following the intermingling, single-particle mass spectra allow us to track individual particle composition as the populations mix via gas-phase exchange. This allows us to explore the mixing and coating behavior of organic-aerosol populations under conditions much closer to concentrations found in the real world.

  7. Radiative forcing under mixed aerosol conditions

    NASA Astrophysics Data System (ADS)

    GarcíA, O. E.; Expósito, F. J.; DíAz, J. P.; DíAz, A. M.

    2011-01-01

    The mixture of mineral dust with biomass burning or urban-industrial aerosols presents significant differences in optical properties when compared to those of the individual constituents, leading to different impacts on solar radiation levels. This effect is assessed by estimating the direct radiative forcing (ΔF) of these aerosols from solar flux models using the radiative parameters derived from the Aerosol Robotic Network (AERONET). These data reveal that, in oceanic and vegetative covers (surface albedo (SA) < 0.30), the aerosol effect at the top of atmosphere (TOA) is always cooling the Earth-atmosphere system, regardless of the aerosol type. The obtained average values of ΔF range between -27 ± 15 Wm-2 (aerosol optical depth (AOD) at 0.55 μm, 0.3 ± 0.3) for mineral dust mixed with urban-industrial aerosols, registered in the East Asia region, and -34 ± 18 Wm-2 (AOD = 0.8 ± 0.4) for the mixture of the mineral dust and biomass burning particles, observed in the Central Africa region. In the intermediate SA range (0.30-0.50) the TOA radiative effect depends on the aerosol absorption properties. Thus, aerosols with single scattering albedo at 0.55 μm lower than ˜0.88 lead to a warming of the system, with ΔF of 10 ± 11 Wm-2 for the mixture of mineral dust and biomass burning. Cases with SA > 0.30 are not present in East Asia region. At the bottom of atmosphere (BOA) the maximum ΔF values are associated with the highest AOD levels obtained for the mixture of mineral dust and biomass burning aerosols (-130 ± 44 Wm-2 with AOD = 0.8 ± 0.4 for SA < 0.30).

  8. Influences of external vs. core-shell mixing on aerosol optical properties at various relative humidities.

    PubMed

    Ramachandran, S; Srivastava, Rohit

    2013-05-01

    Aerosol optical properties of external and core-shell mixtures of aerosol species present in the atmosphere are calculated in this study for different relative humidities. Core-shell Mie calculations are performed using the values of radii, refractive indices and densities of aerosol species that act as core and shell, and the core-shell radius ratio. The single scattering albedo (SSA) is higher when the absorbing species (black carbon, BC) is the core, while for a sulfate core SSA does not vary significantly as the BC in the shell dominates the absorption. Absorption gets enhanced in core-shell mixing of absorbing and scattering aerosols when compared to their external mixture. Thus, SSA is significantly lower for a core-shell mixture than their external mixture. SSA is more sensitive to core-shell ratio than mode radius when BC is the core. The extinction coefficient, SSA and asymmetry parameter are higher for external mixing when compared to BC (core)-water soluble aerosol (shell), and water soluble aerosol (core)-BC (shell) mixtures in the relative humidity range of 0 to 90%. Spectral SSA exhibits the behaviour of the species which acts as a shell in core-shell mixing. The asymmetry parameter for an external mixture of water soluble aerosol and BC is higher than BC (core)-water soluble aerosol (shell) mixing and increases as function of relative humidity. The asymmetry parameter for the water soluble aerosol (core)-BC (shell) is independent of relative humidity as BC is hydrophobic. The asymmetry parameter of the core-shell mixture decreases when BC aerosols are involved in mixing, as the asymmetry parameter of BC is lower. Aerosol optical depth (AOD) of core-shell mixtures increases at a higher rate when the relative humidity exceeds 70% in continental clean and urban aerosol models, whereas AOD remains the same when the relative humidity exceeds 50% in maritime aerosol models. The SSA for continental aerosols varies for core-shell mixing of water soluble

  9. Development of a low-pressure "counterflow exchanging virtual impactor" for aerosol analysis, and, Measurement of ozone mixing ratios and meteorological parameters through the boundary layer at Summit, Greenland

    NASA Astrophysics Data System (ADS)

    Boulter, James Edward

    Trace atmospheric gases may provide significant interferences for in situ chemical analyses of atmospheric particles. Hence, a continuous technique to selectively remove the aerosol fraction from ambient air is desirable. A low-pressure "counterflow exchanging virtual impactor" (LP-CEVI), based upon the principle of inertial particle impaction, was developed to exchange aerosol particles larger than a certain aerodynamic size into a stream of inert gas while excluding atmospheric gases. Impactor particle transmission was characterized by two experimental techniques, one utilizing condensation particle counting of size-selected, nebulized salt particles and the other utilizing filter collection and extraction of monodisperse fluorescent microspheres. The impactor was also characterized for the ability to exclude ambient air, using the detection of nitric oxide by gas-phase chemiluminescence resulting from its reaction with ozone. Within certain pressure and counterflow regimes, the LP-CEVI was found to reproducibly transmit particles greater than approximately 0.2 mum in diameter while excluding more than 99.9% of ambient gas from the particle stream. Potential applications of the impactor to laboratory and field studies are discussed. Chemical processes occurring in firn air, interstitial air within the top several centimeters of snowpack, are important to understanding the composition of the Arctic troposphere. Research was conducted at Summit, Greenland in June 2000 to measure vertical profiles of the ozone mixing ratio and various meteorological parameters through the top of the boundary layer from tethered helium balloon platforms. Ozone mixing ratio profiles were measured using electrochemical ozonesondes in addition to a compact, lightweight, single-beam UV absorbance ozone instrument designed for field use. Profiles of meteorological parameters such as temperature, water vapor pressure, wind speed, and wind direction were measured using radiosondes and

  10. Tower Water-Vapor Mixing Ratio

    SciTech Connect

    Guastad, Krista; Riihimaki, Laura; none,

    2013-04-01

    The purpose of the Tower Water-Vapor Mixing Ratio (TWRMR) value-added product (VAP) is to calculate water-vapor mixing ratio at the 25-meter and 60-meter levels of the meteorological tower at the Southern Great Plains (SGP) Central Facility.

  11. Mixing state of aerosols over the Indo-Gangetic Plain: Radiative forcing and heating rate

    NASA Astrophysics Data System (ADS)

    Srivastava, R.; Ramachandran, S.

    2012-12-01

    ratio is calculated from the geometry of core-shell particles, which depends on the mass and density of the core and shell. The size distribution parameters and refractive indices of different aerosol species are taken from OPAC database [3]. Different fractions of black carbon, water soluble and mineral dust aerosols involved in core-shell mixing emerge as the most probable mixing states over the IGP. Aerosol forcing for external mixing shows higher deviations from those for probable mixing cases during winter and pre-monsoon. The heating rate over Kanpur and Gandhi College in the lower troposphere is similar during pre-monsoon (March-May) ( 0.75 K day^{-1}) and monsoon (June-September) ( 0.5 K day^{-1}), while differences occur in other seasons [4]. Aerosol heating rate profiles exhibit primary and secondary peaks over the IGP and exhibit seasonal variations. Details on the calculations of aerosol mixing states over IGP, the impact of aerosol mixing state on aerosol forcing and heating rate will be discussed. References: [1] Intergovernmental panel on climate change (2007), Solomon S. et al. (eds.), Cambridge Univ. Press, NewYork. [2] Holben B. N., et al. (2001), J. Geophys. Res., 106(D11), 12067-12097. [3] Hess M., P. Koepke, I. Schult (1998), Bull. Am. Meteorol. Soc., 79, 831-844. [4] Srivastava R., S. Ramachandran (2012), Q. J. R. Meteorol. Soc., 138, doi:10.1002/qj.1958.

  12. Flowmeter determines mix ratio for viscous adhesives

    NASA Technical Reports Server (NTRS)

    Lemons, C. R.

    1967-01-01

    Flowmeter determines mix ratio for continuous flow mixing machine used to produce an adhesive from a high viscosity resin and aliphatic amine hardener pumped through separate lines to a rotary blender. The flowmeter uses strain gages in the two flow paths and monitors their outputs with appropriate instrumentation.

  13. New Examination of the Traditional Raman Lidar Technique II: Evaluating the Ratios for Water Vapor and Aerosols

    NASA Technical Reports Server (NTRS)

    Whiteman, David N.

    2003-01-01

    In a companion paper, the temperature dependence of Raman scattering and its influence on the Raman and Rayleigh-Mie lidar equations was examined. New forms of the lidar equation were developed to account for this temperature sensitivity. Here those results are used to derive the temperature dependent forms of the equations for the water vapor mixing ratio, aerosol scattering ratio, aerosol backscatter coefficient, and extinction to backscatter ratio (Sa). The error equations are developed, the influence of differential transmission is studied and different laser sources are considered in the analysis. The results indicate that the temperature functions become significant when using narrowband detection. Errors of 5% and more can be introduced in the water vapor mixing ratio calculation at high altitudes and errors larger than 10% are possible for calculations of aerosol scattering ratio and thus aerosol backscatter coefficient and extinction to backscatter ratio.

  14. A conceptual framework for mixing structures in individual aerosol particles

    NASA Astrophysics Data System (ADS)

    Li, Weijun; Sun, Jiaxing; Xu, Liang; Shi, Zongbo; Riemer, Nicole; Sun, Yele; Fu, Pingqing; Zhang, Jianchao; Lin, Yangting; Wang, Xinfeng; Shao, Longyi; Chen, Jianmin; Zhang, Xiaoye; Wang, Zifa; Wang, Wenxing

    2016-11-01

    This study investigated the particle size- and age-dependent mixing structures of individual particles in clean and polluted air. Aerosols were classified into eight components: sea salt, mineral dust, fly ash, metal, soot, sulfates, nitrates, and organic matter (OM). Based on our aerosol classification, a particle that consists of two or more aerosol components can be defined as an internally mixed particle. Otherwise, it is considered to be an externally mixed particle. Within the internally mixed particle class, we identified four heterogeneous mixing structures: core-shell, dumbbell, OM coating, and dispersed OM, as well as one homogeneous-like mixing structure. Homogeneous-like mixing mainly occurred in fine particles (<1 µm), while the frequency of heterogeneously mixed particles increased with particle size. Our study demonstrated that particle mixing structures depend on particle size and location and evolve with time. OM-coating and core-shell structures are important indicators for particle aging in air as long as they are distant from specific emission sources. Long-range transported particles tended to have core-shell and OM-coating structures. We found that secondary aerosol components (e.g., sulfates, nitrates, and organics) determined particle mixing structures, because their phases change following particle hydration and dehydration under different relative humidities. Once externally mixed particles are transformed into internally mixed particles, they cannot revert to their former state, except when semivolatile aerosol components are involved. Categorizing mixing structures of individual particles is essential for studying their optical and hygroscopic properties and for tracing the development of their physical or chemical properties over time.

  15. Golden ratio prediction for solar neutrino mixing

    SciTech Connect

    Kajiyama, Yuji; Raidal, Martti; Strumia, Alessandro

    2007-12-01

    We present a simple texture that predicts the cotangent of the solar neutrino mixing angle to be equal to the golden ratio. This prediction is 1.4{sigma} below the present best-fit value and final SNO and KamLAND data could discriminate it from tri-bimaximal mixing. The neutrino mass matrix is invariant under a Z{sub 2} x Z{sub 2}{sup '} symmetry: that geometrically is a reflection along the diagonal of the golden rectangle. Assuming an analogous structure in the quark sector suggests a golden prediction for the Cabibbo angle, {theta}{sub C}={pi}/4-{theta}{sub 12}{approx_equal}13.3 deg., up to the uncertainties comparable to V{sub ub}.

  16. CO (Carbon Monoxide Mixing Ratio System) Handbook

    SciTech Connect

    Biraud, S

    2011-02-23

    The main function of the CO instrument is to provide continuous accurate measurements of carbon monoxide mixing ratio at the ARM SGP Central Facility (CF) 60-meter tower (36.607 °N, 97.489 °W, 314 meters above sea level). The essential feature of the control and data acquisition system is to record signals from a Thermo Electron 48C and periodically calibrate out zero and span drifts in the instrument using the combination of a CO scrubber and two concentrations of span gas (100 and 300 ppb CO in air). The system was deployed on May 25, 2005.

  17. Using Retrieved Aerosol Spectral Properties to Characterize Aerosol Composition and Mixing

    NASA Astrophysics Data System (ADS)

    Li, J.

    2015-12-01

    The spectral dependence of aerosol properties, such as aerosol absorption optical depth (AAOD) and single scattering albedo (SSA), can be used to infer aerosol composition. In particular, aerosol mixtures dominated by dust absorption will have monotonically increasing SSA with wavelength while that dominated by black carbon absorption has monotonically decreasing SSA spectra. However, spectral AAOD and SSA measured in reality may differ from these extreme cases, due to the complicated composition and mixing states. In this study, we use spectral SSA and AAOD retrieved from AERONET measurements, assisted by CALIPSO aerosol type product and Mie calculations, to characterize aerosol mixtures over representative regions. Moreover, in addition to the monotonically increasing or decreasing AAOD and SSA spectra, we find the spectral dependence of these two parameters are frequently peaked (at 675 nm or 870 nm) over several places including East Asia, India, West Africa and South America. We thus suggest that SSA spectral curvature, defined as the negative of the second derivative of SSA as a function of wavelength, can provide additional information on the composition of these aerosol mixtures. Further analysis indicates that moderate mixing of black carbon with dust or organic carbon is mainly responsible for producing the SSA curvature. An optimization scheme was developed to match the observed AAOD and SSA spectra with Mie calculations assuming different aerosol composition and mixing states. Results suggest that while external mixing can explain most of the observed AAOD and SSA spectral dependence, internal mixing or core-shell mode is also likely under many circumstances, such as East Asia during winter and post-monsoon and winter seasons over India. This method offers the potential to quantitatively infer aerosol composition from these spectral measurements of aerosol optical properties.

  18. Study of atmospheric aerosols and mixing layer by LIDAR.

    PubMed

    Angelini, Federico; Barnaba, Francesca; Landi, Tony Christian; Caporaso, Luca; Gobbi, Gian Paolo

    2009-12-01

    The LIDAR (laser radar) is an active remote sensing technique, which allows for the altitude-resolved observation of several atmospheric constituents. A typical application is the measurement of the vertically resolved aerosol optical properties. By using aerosol particles as a marker, continuous determination of the mixing layer height (MLH) can also be obtained by LIDAR. Some examples of aerosol extinction coefficient profiles and MLH extracted from a 1-year LIDAR data set collected in Milan (Italy) are discussed and validated against in situ data (from a balloon-borne optical particle counter). Finally a comparison of the observation-based MLH with relevant numerical simulations (mesoscale model MM5) is provided.

  19. On the mixing and evaporation of secondary organic aerosol components.

    PubMed

    Loza, Christine L; Coggon, Matthew M; Nguyen, Tran B; Zuend, Andreas; Flagan, Richard C; Seinfeld, John H

    2013-06-18

    The physical state and chemical composition of an organic aerosol affect its degree of mixing and its interactions with condensing species. We present here a laboratory chamber procedure for studying the effect of the mixing of organic aerosol components on particle evaporation. The procedure is applied to the formation of secondary organic aerosol (SOA) from α-pinene and toluene photooxidation. SOA evaporation is induced by heating the chamber aerosol from room temperature (25 °C) to 42 °C over 7 h and detected by a shift in the peak diameter of the SOA size distribution. With this protocol, α-pinene SOA is found to be more volatile than toluene SOA. When SOA is formed from the two precursors sequentially, the evaporation behavior of the SOA most closely resembles that of SOA from the second parent hydrocarbon, suggesting that the structure of the mixed SOA resembles a core of SOA from the initial precursor coated by a layer of SOA from the second precursor. Such a core-and-shell configuration of the organic aerosol phases implies limited mixing of the SOA from the two precursors on the time scale of the experiments, consistent with a high viscosity of at least one of the phases.

  20. Development of the RAQM2 aerosol chemical transport model and predictions of the Northeast Asian aerosol mass, size, chemistry, and mixing type

    NASA Astrophysics Data System (ADS)

    Kajino, M.; Inomata, Y.; Sato, K.; Ueda, H.; Han, Z.; An, J.; Katata, G.; Deushi, M.; Maki, T.; Oshima, N.; Kurokawa, J.; Ohara, T.; Takami, A.; Hatakeyama, S.

    2012-12-01

    A new aerosol chemical transport model, the Regional Air Quality Model 2 (RAQM2), was developed to simulate the Asian air quality. We implemented a simple version of a triple-moment modal aerosol dynamics model (MADMS) and achieved a completely dynamic (non-equilibrium) solution of a gas-to-particle mass transfer over a wide range of aerosol diameters from 1 nm to super-μm. To consider a variety of atmospheric aerosol properties, a category approach was utilized in which the aerosols were distributed into four categories: particles in the Aitken mode (ATK), soot-free particles in the accumulation mode (ACM), soot aggregates (AGR), and particles in the coarse mode (COR). The aerosol size distribution in each category is characterized by a single mode. The condensation, evaporation, and Brownian coagulations for each mode were solved dynamically. A regional-scale simulation (Δx = 60 km) was performed for the entire year of 2006 covering the Northeast Asian region. The modeled PM1/bulk ratios of the chemical components were consistent with observations, indicating that the simulated aerosol mixing types were consistent with those in nature. The non-sea-salt SO42- mixed with ATK + ACM was the largest at Hedo in summer, whereas the SOSO42- was substantially mixed with AGR in the cold seasons. Ninety-eight percent of the modeled NO3- was mixed with sea salt at Hedo, whereas 53.7% of the NO3- was mixed with sea salt at Gosan, which is located upwind toward the Asian continent. The condensation of HNO3 onto sea salt particles during transport over the ocean accounts for the difference in the NO3- mixing type at the two sites. Because the aerosol mixing type alters the optical properties and cloud condensation nuclei activity, its accurate prediction and evaluation are indispensable for aerosol-cloud-radiation interaction studies.

  1. Aerosol penetration ratio: a new index of ventilation

    SciTech Connect

    Sirr, S.A.; Elliott, G.R.; Regelmann, W.E.; Juenemann, P.J.; Morin, R.L.; Boudreau, R.J.; Warwick, W.J.; Loken, M.K.

    1986-08-01

    Superimposition of nuclear medicine scintigrams and standard radiographs provides a unique opportunity for merging functional information intrinsic to nuclear medicine images with the high resolution anatomic detail of radiographs. A newly developed image processing system allows the merging of two separate films of greatly varying sizes to form a single composite image. Subsequent quantitative analysis of the composite image may be performed. Using the superimposition technique, (/sup 99m/Tc)DTPA aerosol ventilation scans (4.5 X 4.5 cm) were superimposed upon chest radiographs (35.6 X 43.2 cm) in 17 cystic fibrosis (CF) patients. Subsequent quantification of the area of nuclear scan ventilation and the radiographic lung area was then performed. A new quantitative radiologic index of ventilation, the aerosol penetration ratio (APR), was defined. Linear correlation of aerosol penetration ratio with residual volume (RV) as percent of total lung capacity (TLC) measured by body plethysmography was good. We conclude that the APR has validity as a physiologic parameter which localized regional excessive residual volume and correlates well with RV/TLC, the gold standard pulmonary function index of obstructive airway disease.

  2. Accurate and precise zinc isotope ratio measurements in urban aerosols.

    PubMed

    Gioia, Simone; Weiss, Dominik; Coles, Barry; Arnold, Tim; Babinski, Marly

    2008-12-15

    We developed an analytical method and constrained procedural boundary conditions that enable accurate and precise Zn isotope ratio measurements in urban aerosols. We also demonstrate the potential of this new isotope system for air pollutant source tracing. The procedural blank is around 5 ng and significantly lower than published methods due to a tailored ion chromatographic separation. Accurate mass bias correction using external correction with Cu is limited to Zn sample content of approximately 50 ng due to the combined effect of blank contribution of Cu and Zn from the ion exchange procedure and the need to maintain a Cu/Zn ratio of approximately 1. Mass bias is corrected for by applying the common analyte internal standardization method approach. Comparison with other mass bias correction methods demonstrates the accuracy of the method. The average precision of delta(66)Zn determinations in aerosols is around 0.05 per thousand per atomic mass unit. The method was tested on aerosols collected in Sao Paulo City, Brazil. The measurements reveal significant variations in delta(66)Zn(Imperial) ranging between -0.96 and -0.37 per thousand in coarse and between -1.04 and 0.02 per thousand in fine particular matter. This variability suggests that Zn isotopic compositions distinguish atmospheric sources. The isotopic light signature suggests traffic as the main source. We present further delta(66)Zn(Imperial) data for the standard reference material NIST SRM 2783 (delta(66)Zn(Imperial) = 0.26 +/- 0.10 per thousand).

  3. CCN activation of fumed silica aerosols mixed with soluble pollutants

    NASA Astrophysics Data System (ADS)

    Dalirian, M.; Keskinen, H.; Ahlm, L.; Ylisirniö, A.; Romakkaniemi, S.; Laaksonen, A.; Virtanen, A.; Riipinen, I.

    2015-04-01

    Particle-water interactions of completely soluble or insoluble particles are fairly well understood but less is known of aerosols consisting of mixtures of soluble and insoluble components. In this study, laboratory measurements were performed to investigate cloud condensation nuclei (CCN) activity of silica particles mixed with ammonium sulfate (a salt), sucrose (a sugar) and bovine serum albumin known as BSA (a protein). The agglomerated structure of the silica particles was investigated using measurements with a differential mobility analyser (DMA) and an aerosol particle mass analyser (APM). Based on these data, the particles were assumed to be compact agglomerates when studying their CCN activation capabilities. Furthermore, the critical supersaturations of particles consisting of pure and mixed soluble and insoluble compounds were explored using existing theoretical frameworks. These results showed that the CCN activation of single-component particles was in good agreement with Köhler- and adsorption theory based models when the agglomerated structure was accounted for. For mixed particles the CCN activation was governed by the soluble components, and the soluble fraction varied considerably with particle size for our wet-generated aerosols. Our results confirm the hypothesis that knowing the soluble fraction is the key parameter needed for describing the CCN activation of mixed aerosols, and highlight the importance of controlled coating techniques for acquiring a detailed understanding of the CCN activation of atmospheric insoluble particles mixed with soluble pollutants.

  4. Stable lead isotope ratios in Alaskan arctic aerosols

    NASA Astrophysics Data System (ADS)

    Sturges, W. T.; Hopper, J. F.; Barrie, L. A.; Schnell, R. C.

    Aerosol samples collected at Barrow, Alaska, during February and March 1990 were found to have uniform stable lead isotope compositions. The mean 208Pb/ 207Pb ratio was 2.423±0.009 and the mean 206Pb/ 207Pb ratio was 1.161±0.014. The latter ratio is essentially the same as that obtained from an earlier study of aerosols at two Canadian stations in the High Arctic and is typical of, but not unique to, Eurasian sources of atmospheric lead. Further discriminating power was available in this study through the inclusion of 208Pb/ 207Pb ratios, which provided additional evidence that the former Soviet Union and eastern Europe are major contributors to atmospheric particulate lead in the Alaskan Arctic, accounting for around two-thirds of the particulate lead measured at Barrow. The remaining third of the lead is attributed to west European sources. There was no evidence for a substantial North American component, other than local contamination.

  5. Effects of morphology on the radiative properties of internally mixed light absorbing carbon aerosols with different aging status.

    PubMed

    Cheng, Tianhai; Wu, Yu; Chen, Hao

    2014-06-30

    Light absorbing carbon aerosols play a substantial role in climate change through radiative forcing, which is the dominant absorber of solar radiation. Radiative properties of light absorbing carbon aerosols are strongly dependent on the morphological factors and the mixing mechanism of black carbon with other aerosol components. This study focuses on the morphological effects on the optical properties of internally mixed light absorbing carbon aerosols using the numerically exact superposition T-matrix method. Three types aerosols with different aging status such as freshly emitted BC particles, thinly coated light absorbing carbon aerosols, heavily coated light absorbing carbon aerosols are studied. Our study showed that morphological factors change with the aging of internally mixed light absorbing carbon aerosols to result in a dramatic change in their optical properties. The absorption properties of light absorbing carbon aerosols can be enhanced approximately a factor of 2 at 0.67 um, and these enhancements depend on the morphological factors. A larger shell/core diameter ratio of volume-equivalent shell-core spheres (S/C), which indicates the degree of coating, leads to stronger absorption. The enhancement of absorption properties accompanies a greater enhancement of scattering properties, which is reflected in an increase in single scattering albedo (SSA). The enhancement of single scattering albedo due to the morphological effects can reach a factor of 3.75 at 0.67 μm. The asymmetry parameter has a similar yet smaller enhancement. Moreover, the corresponding optical properties of shell-and-core model determined by using Lorenz -Mie solutions are presented for comparison. We found that the optical properties of internally mixed light absorbing carbon aerosol can differ fundamentally from those calculated for the Mie theory shell-and-core model, particularly for thinly coated light absorbing carbon aerosols. Our studies indicate that the complex morphology

  6. 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

  7. Using the Aerosol Single Scattering Albedo and Angstrom Exponent from AERONET to Determine Aerosol Origins and Mixing States over the Indo-Gangetic Plain

    NASA Astrophysics Data System (ADS)

    Giles, D. M.; Holben, B. N.; Eck, T. F.; Sinyuk, A.; Slutsker, I.; Smirnov, A.; Schafer, J. S.; Dickerson, R. R.; Thompson, A. M.; Tripathi, S. N.; Singh, R. P.; Ghauri, B.

    2012-12-01

    various fuel types (e.g., from open agricultural waste, forest, or dung burning), combustion phases, or aging processes including aggregation or mixing with ambient aerosols. Other intensive aerosol properties (e.g., depolarization ratio or absorption Angstrom exponent) may provide improved definition of fine mode dominated aerosol types from U/I and BB sources [Burton et al., 2012, Giles et al., 2012]. Additional sites in India and Pakistan are also analyzed using available AERONET Version 2, Level 2.0 data.

  8. Optical properties of mixed aerosol layers over Japan derived with multi-wavelength Mie-Raman lidar system

    NASA Astrophysics Data System (ADS)

    Hara, Yukari; Nishizawa, Tomoaki; Sugimoto, Nobuo; Matsui, Ichiro; Pan, Xiaole; Kobayashi, Hiroshi; Osada, Kazuo; Uno, Itsushi

    2017-02-01

    Mixing state of aerosols and optical properties including lidar ratio, particle depolarization ratio, and Ångström exponent were investigated at Fukuoka in western Japan using a multi-wavelength Mie-Raman lidar (MMRL), various aerosol mass-concentration measurements, and a polarization optical particle counter during Winter-Spring 2015. Aerosol extinction coefficient, backscatter coefficient, and depolarization at 355 and 532 nm and attenuated backscatter coefficient at 1064 nm are obtained from the MMRL measurements. Ten aerosol episodes were classified into three categories (air pollution, mineral dust, and marine aerosol) based on aerosol mass-concentration measurements in the fine-mode (particle diameter Dp<2.5 μm) and coarse-mode (2.5 μmratio for air pollution was 57±4 sr at 355 nm and 53±8 sr at 532 nm with Ångström exponent of 1.4±0.5. For mineral dust, a slightly high averaged lidar ratio (50±7 sr at 355 nm and 54±9 sr at 532 nm) was obtained with relatively high Ångström exponent of 0.8±0.3 owing to contributions from fine-mode particles (PMf). The mean particle depolarization ratios of 13±8% at 355 nm and 16±6% at 532 nm also suggest mixing of mineral dust and anthropogenic fine-mode aerosols. The lowest lidar ratio was obtained for marine case. Classification of aerosol types using the lidar ratio and particle depolarization ratio was conducted based on the results obtained in this study. The classified aerosol types almost corresponded to aerosol category obtained by previous studies. We found no remarkable correlation between the fraction of black carbon and the lidar ratio: this might be due to the complexity of the mixing state among various aerosols. The obtained lidar ratio was rather correlated with the ratio of PMf to PM10, representing the mixing state of fine- and coarse-mode particles.

  9. Spray Gun With Constant Mixing Ratio

    NASA Technical Reports Server (NTRS)

    Simpson, William G.

    1987-01-01

    Conceptual mechanism mounted in handle of spray gun maintains constant ratio between volumetric flow rates in two channels leading to spray head. With mechanism, possible to keep flow ratio near 1:1 (or another desired ratio) over range of temperatures, orifice or channel sizes, or clogging conditions.

  10. Measurement of Sulfur Isotope Ratios in Micrometer-Sized Aerosol Samples by NanoSIMS

    NASA Astrophysics Data System (ADS)

    Winterholler, B.; Hoppe, P.; Foley, S.; Andreae, M. O.

    2005-12-01

    The isotopic composition of sulfur in the atmosphere is highly variable and source dependent. Sulfur isotopic ratios are a well established tool for identifying sources of sulfur in the environment, estimating emission factors, and tracing the spread of sulfur from anthropogenic point sources in terrestrial ecosystems. Conventional mass spectrometry needs a minimum of 1 micromol of sulfur to perform one analysis. In the case of atmospheric aerosol particles the results of such an analysis averages the isotopic compositions of millions of aerosol particles, and thus normally includes several different types of sulfur aerosol. The new Cameca NanoSIMS 50 ion microprobe technique permits analysis of individual aerosol particles with volumes down to 0.3 cubic micron and a precision for delta34S of 3-10 (2 sigma). As a result, this technique is able to introduce a new scale into the study of the atmospheric sulfur cycle. Linking the chemical, mineralogical, morphological and isotopic information of individual particles will allow a better understanding of external and internal mixing states by analyzing more than one spot on coarse mode particles. Moreover it will improve source identification by complementing the chemical and isotopic information. First samples have been collected from the Sahara desert, an urban site in central Europe, and a costal site in Western Ireland and show the potentials of this new technique.

  11. Retrieving the aerosol lidar ratio profile by combining ground- and space-based elastic lidars.

    PubMed

    Feiyue, Mao; Wei, Gong; Yingying, Ma

    2012-02-15

    The aerosol lidar ratio is a key parameter for the retrieval of aerosol optical properties from elastic lidar, which changes largely for aerosols with different chemical and physical properties. We proposed a method for retrieving the aerosol lidar ratio profile by combining simultaneous ground- and space-based elastic lidars. The method was tested by a simulated case and a real case at 532 nm wavelength. The results demonstrated that our method is robust and can obtain accurate lidar ratio and extinction coefficient profiles. Our method can be useful for determining the local and global lidar ratio and validating space-based lidar datasets.

  12. A variable mixing-length ratio for convection theory

    NASA Technical Reports Server (NTRS)

    Chan, K. L.; Wolff, C. L.; Sofia, S.

    1981-01-01

    It is argued that a natural choice for the local mixing length in the mixing-length theory of convection has a value proportional to the local density scale height of the convective bubbles. The resultant variable mixing-length ratio (the ratio between the mixing length and the pressure scale height) of this theory is enhanced in the superadiabatic region and approaches a constant in deeper layers. Numerical tests comparing the new mixing length successfully eliminate most of the density inversion that typically plagues conventional results. The new approach also seems to indicate the existence of granular motion at the top of the convection zone.

  13. Aerosol optical properties and mixing state of black carbon in the Pearl River Delta, China

    NASA Astrophysics Data System (ADS)

    Tan, Haobo; Liu, Li; Fan, Shaojia; Li, Fei; Yin, Yan; Cai, Mingfu; Chan, P. W.

    2016-04-01

    Aerosols contribute the largest uncertainty to the total radiative forcing estimate, and black carbon (BC) that absorbs solar radiation plays an important role in the Earth's energy budget. This study analysed the aerosol optical properties from 22 February to 18 March 2014 at the China Meteorological Administration Atmospheric Watch Network (CAWNET) station in the Pearl River Delta (PRD), China. The representative values of dry-state particle scattering coefficient (σsp), hemispheric backscattering coefficient (σhbsp), absorption coefficient (σabsp), extinction coefficient (σep), hemispheric backscattering fraction (HBF), single scattering albedo (SSA), as well as scattering Ångström exponent (α) were presented. A comparison between a polluted day and a clean day shows that the aerosol optical properties depend on particle number size distribution, weather conditions and evolution of the mixing layer. To investigate the mixing state of BC at the surface, an optical closure study of HBF between measurements and calculations based on a modified Mie model was employed for dry particles. The result shows that the mixing state of BC might be between the external mixture and the core-shell mixture. The average retrieved ratio of the externally mixed BC to the total BC mass concentration (rext-BC) was 0.58 ± 0.12, and the diurnal pattern of rext-BC can be found. Furthermore, considering that non-light-absorbing particles measured by a Volatility-Tandem Differential Mobility Analyser (V-TDMA) exist independently with core-shell and homogenously internally mixed BC particles, the calculated optical properties were just slightly different from those based on the assumption that BC exist in each particle. This would help understand the influence of the BC mixing state on aerosol optical properties and radiation budget in the PRD.

  14. Changes in monoterpene mixing ratios during summer storms in rural New Hampshire (USA)

    USGS Publications Warehouse

    Haase, K.B.; Jordan, C.; Mentis, E.; Cottrell, L.; Mayne, H.R.; Talbot, R.; Sive, B.C.

    2011-01-01

    Monoterpenes are an important class of biogenic hydrocarbons that influence ambient air quality and are a principle source of secondary organic aerosol (SOA). Emitted from vegetation, monoterpenes are a product of photosynthesis and act as a response to a variety of environmental factors. Most parameterizations of monoterpene emissions are based on clear weather models that do not take into account episodic conditions that can drastically change production and release rates into the atmosphere. Here, the ongoing monoterpene dataset from the rural Thompson Farm measurement site in Durham, New Hampshire is examined in the context of a set of known severe storm events. While some storm systems had a negligible influence on ambient monoterpene mixing ratios, the average storm event increased mixing ratios by 0.59 ?? 0.21 ppbv, a factor of 93 % above pre-storm levels. In some events, mixing ratios reached the 10's of ppbv range and persisted overnight. These mixing ratios correspond to increases in the monoterpene emission rate, ranging from 120 to 1240 g km-2 h -1 compared to an estimated clear weather rate of 116 to 193 g km-2 h-1. Considering the regularity of storm events over most forested areas, this could be an important factor to consider when modeling global monoterpene emissions and their resulting influence on the formation of organic aerosols. ?? 2011 Author(s).

  15. Changes in monoterpene mixing ratios during summer storms in rural New Hampshire (USA)

    USGS Publications Warehouse

    Haase, Karl B.; Jordan, C.; Mentis, E.; Cottrell, L.; Mayne, H.R.; Talbot, R.; Sive, B.C.

    2011-01-01

    Monoterpenes are an important class of biogenic hydrocarbons that influence ambient air quality and are a principle source of secondary organic aerosol (SOA). Emitted from vegetation, monoterpenes are a product of photosynthesis and act as a response to a variety of environmental factors. Most parameterizations of monoterpene emissions are based on clear weather models that do not take into account episodic conditions that can drastically change production and release rates into the atmosphere. Here, the monoterpene dataset from the rural Thompson Farm measurement site in Durham, New Hampshire is examined in the context of a set of known severe storm events. While some storm systems had a negligible influence on ambient monoterpene mixing ratios, the average storm event increased mixing ratios by 0.59 ?? 0.21 ppbv, a factor of 93% above pre-storm levels. In some events, mixing ratios reached the 10's of ppbv range and persisted overnight. These mixing ratios correspond to increases in the monoterpene emission rate, ranging from 120 to 1240 g km-2 h -1 compared to an estimated clear weather rate of 116 to 193 g km-2 h-1. Considering the regularity of storm events over most forested areas, this could be an important factor to consider when modeling global monoterpene emissions and their resulting influence on the formation of organic aerosols.

  16. Investigate the relationship between multiwavelength lidar ratios and aerosol size distributions using aerodynamic particle sizer spectrometer

    NASA Astrophysics Data System (ADS)

    Zhao, Hu; Hua, Dengxin; Mao, Jiandong; Zhou, Chunyan

    2017-02-01

    The real aerosol size distributions were obtained by aerodynamic particle sizer spectrometer (APS) in China YinChuan. The lidar ratios at wavelengths of 355 nm, 532 nm and 1064 nm were calculated using Mie theory. The effective radius of aerosol particles reff and volume C/F ratio (coarse/fine) Vc/f were retrieved from the real aerosol size distributions. The relationship between multiwavelength lidar ratios and particle reff and Vc/f were investigated. The results indicate that the lidar ratio is positive correlated to the particle reff and Vc/f. The lidar ratio is more sensitive to the coarse particles. The short wavelength lidar ratio is more sensitive to the particle Vc/f and the long wavelength lidar ratio is more sensitive to the particle reff. The wavelength dependency indicated that the lidar ratios decrease with increasing the wavelength. The lidar ratios are almost irrelevant to the shape and total particles of aerosol size distributions.

  17. MATRIX (Multiconfiguration Aerosol TRacker of mIXing state): an aerosol microphysical module for global atmospheric models

    NASA Astrophysics Data System (ADS)

    Bauer, S. E.; Wright, D.; Koch, D.; Lewis, E. R.; McGraw, R.; Chang, L.-S.; Schwartz, S. E.; Ruedy, R.

    2008-05-01

    A new aerosol microphysical module MATRIX, the Multiconfiguation Aerosol TRacker of mIXing state, and its application in the Goddard Institute for Space Studies (GISS) climate model (ModelE) is described. This module, which is based on the quadrature method of moments (QMOM), represents nucleation, condensation, coagulation, internal and external mixing, and cloud-drop activation and provides aerosol particle mass and number concentration and particle size information for up to 16 mixed-mode aerosol populations. Internal and external mixing among aerosol components sulfate, nitrate, ammonium, carbonaceous aerosols, dust and sea-salt particles are represented. The solubility of each aerosol mode, which is explicitly calculated based on its soluble and insoluble components, enables calculation of the dependence of cloud drop activation on the microphysical characterization of multiple soluble modes. A detailed model description and results of box-model simulations of various mode configurations are presented. The number concentration of aerosol particles activated to cloud drops depends on the mode configuration. Simulations on the global scale with the GISS climate model are evaluated against aircraft and station measurements of aerosol mass and number concentration and particle size. The model accurately captures the observed size distributions in the aitken and accumulation modes up to particle diameter 1 μm, in which sulfate, nitrate, black and organic carbon are predominantly located; however the model underestimates coarse-mode number concentration and size, especially in the marine environment.

  18. Model analysis of influences of aerosol mixing state upon its optical properties in East Asia

    NASA Astrophysics Data System (ADS)

    Han, Xiao; Zhang, Meigen; Zhu, Lingyun; Xu, Liren

    2013-07-01

    The air quality model system RAMS (Regional Atmospheric Modeling System)-CMAQ (Models-3 Community Multi-scale Air Quality) coupled with an aerosol optical/radiative module was applied to investigate the impact of different aerosol mixing states (i.e., externally mixed, half externally and half internally mixed, and internally mixed) on radiative forcing in East Asia. The simulation results show that the aerosol optical depth (AOD) generally increased when the aerosol mixing state changed from externally mixed to internally mixed, while the single scattering albedo (SSA) decreased. Therefore, the scattering and absorption properties of aerosols can be significantly affected by the change of aerosol mixing states. Comparison of simulated and observed SSAs at five AERONET (Aerosol Robotic Network) sites suggests that SSA could be better estimated by considering aerosol particles to be internally mixed. Model analysis indicates that the impact of aerosol mixing state upon aerosol direct radiative forcing (DRF) is complex. Generally, the cooling effect of aerosols over East Asia are enhanced in the northern part of East Asia (Northern China, Korean peninsula, and the surrounding area of Japan) and are reduced in the southern part of East Asia (Sichuan Basin and Southeast China) by internal mixing process, and the variation range can reach ±5 W m-2. The analysis shows that the internal mixing between inorganic salt and dust is likely the main reason that the cooling effect strengthens. Conversely, the internal mixture of anthropogenic aerosols, including sulfate, nitrate, ammonium, black carbon, and organic carbon, could obviously weaken the cooling effect.

  19. MATRIX (Multiconfiguration Aerosol TRacker of mIXing state): an aerosol microphysical module for global atmospheric models

    NASA Astrophysics Data System (ADS)

    Bauer, S. E.; Wright, D. L.; Koch, D.; Lewis, E. R.; McGraw, R.; Chang, L.-S.; Schwartz, S. E.; Ruedy, R.

    2008-10-01

    A new aerosol microphysical module MATRIX, the Multiconfiguration Aerosol TRacker of mIXing state, and its application in the Goddard Institute for Space Studies (GISS) climate model (ModelE) are described. This module, which is based on the quadrature method of moments (QMOM), represents nucleation, condensation, coagulation, internal and external mixing, and cloud-drop activation and provides aerosol particle mass and number concentration and particle size information for up to 16 mixed-mode aerosol populations. Internal and external mixing among aerosol components sulfate, nitrate, ammonium, carbonaceous aerosols, dust and sea-salt particles are represented. The solubility of each aerosol population, which is explicitly calculated based on its soluble and insoluble components, enables calculation of the dependence of cloud drop activation on the microphysical characterization of multiple soluble aerosol populations. A detailed model description and results of box-model simulations of various aerosol population configurations are presented. The box model experiments demonstrate the dependence of cloud activating aerosol number concentration on the aerosol population configuration; comparisons to sectional models are quite favorable. MATRIX is incorporated into the GISS climate model and simulations are carried out primarily to assess its performance/efficiency for global-scale atmospheric model application. Simulation results were compared with aircraft and station measurements of aerosol mass and number concentration and particle size to assess the ability of the new method to yield data suitable for such comparison. The model accurately captures the observed size distributions in the Aitken and accumulation modes up to particle diameter 1 μm, in which sulfate, nitrate, black and organic carbon are predominantly located; however the model underestimates coarse-mode number concentration and size, especially in the marine environment. This is more likely due to

  20. Oxidative aging of mixed oleic acid/sodium chloride aerosol particles

    NASA Astrophysics Data System (ADS)

    Dennis-Smither, Benjamin J.; Miles, Rachael E. H.; Reid, Jonathan P.

    2012-10-01

    Studies of the oxidative aging of single mixed component aerosol particles formed from oleic acid (OL) and sodium chloride over a range of relative humidities (RH) and ozone concentrations by aerosol optical tweezers are reported. The rate of loss of OL and changes in the organic phase volume are directly measured, comparing particles with effloresced and deliquesced inorganic seeds. The kinetics of the OL loss are analyzed and the value of the reactive uptake coefficient of ozone by OL is compared to previous studies. The reaction of OL is accompanied by a decrease in the particle volume, consistent with the evaporation of semivolatile products over a time scale of tens of thousands of seconds. Measurements of the change in the organic phase volume allow the branching ratio to involatile components to be estimated; between 50 and 85% of the initial organic volume remains involatile, depending on ozone concentration. The refractive index (RI) of the organic phase increases during and after evaporation of volatile products, consistent with aging followed by a slow restructuring in particle morphology. The hygroscopicity of the particle and kinetics of the response of the organic phase to changes in RH are investigated. Both size and RI of unoxidized and oxidized particles respond promptly to RH changes with values of the RI consistent with linear mixing rules. Such studies of the simultaneous changes in composition and size of mixed component aerosol provide valuable data for benchmarking kinetic models of heterogeneous atmospheric aging.

  1. Retrieval of constituent mixing ratios from limb thermal emission spectra

    NASA Technical Reports Server (NTRS)

    Shaffer, William A.; Kunde, Virgil G.; Conrath, Barney J.

    1988-01-01

    An onion-peeling iterative, least-squares relaxation method to retrieve mixing ratio profiles from limb thermal emission spectra is presented. The method has been tested on synthetic data, containing various amounts of added random noise for O3, HNO3, and N2O. The retrieval method is used to obtain O3 and HNO3 mixing ratio profiles from high-resolution thermal emission spectra. Results of the retrievals compare favorably with those obtained previously.

  2. Morphology and Optical Properties of Mixed Aerosol Particles

    NASA Astrophysics Data System (ADS)

    Fard, Mehrnoush M.; Krieger, Ulrich; Rudich, Yinon; Marcolli, Claudia; Peter, Thomas

    2015-04-01

    Experiments and modeling studies have shown that deliquesced aerosols can be present not only as one-phase system containing organics, inorganic salts and water, but often as two-phase systems consisting of a predominantly organic and a predominantly inorganic aqueous phase 1,2. Recent laboratory studies conducted with model mixtures representing tropospheric aerosols1,2,3, secondary organic aerosol (SOA) from smog chamber experiments4, and field measurements5 suggest that liquid- liquid phase separations (LLPS) is indeed a common phenomenon in mixed organic/ ammonium sulfate (AS) particles. During LLPS, particles may adopt different morphologies mainly core- shell and partially engulfed. A core- shell configuration will have consequences for heterogeneous chemistry and hygroscopicity and as a result will alter the optical properties of the particles since the aqueous inorganic-rich phase will be totally enclosed by a probably highly viscous organic coating with low diffusivity for reactants and water. The primary objective of this project is to establish a method for investigating the morphology of mixed inorganic and absorbing organic compounds of atmospheric relevance and study their radiative properties before, during, and after phase transitions mainly during LLPS. This will be the first study looking into the radiative effect of LLPS in detail. In this first experiment, the behavior of single droplets of carminic acid (CA)/ AS/ H2O mixture was monitored during relative humidity (RH) cycles using optical microscopy. The same mixture particle was levitated in an electrodynamic balance (EDB) and the change in its absorption properties was measured at varying RH. We also intend to determine the occurrence of LLPS in accumulation- sized particles and the change in their absorption using a cavity ring down aerosol spectrometer. If LLPS alters the absorptive properties of the suggested model aerosols significantly, absorption measurements of accumulation mode

  3. CFD Assessment of Orifice Aspect Ratio and Mass Flow Ratio on Jet Mixing in Rectangular Ducts

    NASA Technical Reports Server (NTRS)

    Bain, D. B.; Smith, C. E.; Holdeman, J. D.

    1994-01-01

    Isothermal CFD analysis was performed on axially opposed rows of jets mixing with cross flow in a rectangular duct. Laterally, the jets' centerlines were aligned with each other on the top and bottom walls. The focus of this study was to characterize the effects of orifice aspect ratio and jet-to-mainstream mass flow ratio on jet penetration and mixing. Orifice aspect ratios (L/W) of 4-to-1, 2-to-1, and 1-to-1, along with circular holes, were parametrically analyzed. Likewise, jet-to-mainstream mass flow ratios (MR) of 2.0, 0.5, and 0.25 were systematically investigated. The jet-to-mainstream momentum-flux ratio (J) was maintained at 36 for all cases, and the orifice spacing-to-duct height (S/H) was varied until optimum mixing was attained for each configuration. The numerical results showed that orifice aspect ratio (and likewise orifice blockage) had little effect on jet penetration and mixing. Based on mixing characteristics alone, the 4-to-1 slot was comparable to the circular orifice. The 4-to-1 slot has a smaller jet wake which may be advantageous for reducing emissions. However, the axial length of a 4-to-1 slot may be prohibitively long for practical application, especially for MR of 2.0. The jet-to-mainstream mass flow ratio had a more significant effect on jet penetration and mixing. For a 4-to-1 aspect ratio orifice, the design correlating parameter for optimum mixing (C = (S/H)(sq. root J)) varied from 2.25 for a mass flow ratio of 2.0 to 1.5 for a mass flow ratio of 0.25.

  4. Mixing properties of coaxial jets with large velocity ratios and large inverse density ratios

    NASA Astrophysics Data System (ADS)

    Alexander Schumaker, S.; Driscoll, James F.

    2012-05-01

    An experimental study was conducted to better understand the mixing properties of coaxial jets as several parameters were systematically varied, including the velocity ratio, density ratio, and the Reynolds number. Diameters of the inner and outer jet were also varied. Coaxial jets are commonly used to mix fluids due to the simplicity of their geometry and the rapid mixing that they provide. A measure of the overall mixing efficiency is the stoichiometric mixing length (Ls), which is the distance along the jet centerline where the two fluids have mixed to some desired concentration, which was selected to be the stoichiometric concentration for H2/O2 and CH4/O2 in this case. For 56 cases, the profiles of mean mixture fraction, rms mixture fraction fluctuations (unmixedness), and Ls were measured using acetone planar laser induced fluorescence diagnostics. Results were compared to three mixing models. The entrainment model of Villermaux and Rehab showed good agreement with the data, indicating that the proper non-dimensional scaling parameter is the momentum flux ratio M. The work extends the existing database of coaxial jet scalar mixing properties because it considers the specific regime of large values of both the velocity ratio and the inverse density ratio, which is the regime in which rocket injectors operate. Also the work focuses on the mixing up to Ls where previous work focused on the mixing up to the end of the inner core. The Reynolds numbers achieved for a number of cases were considerably larger than previous gas mixing studies, which insures that the jet exit boundary conditions are fully turbulent.

  5. Elucidating carbonaceous aerosol sources by the stable carbon δ13CTC ratio in size-segregated particles

    NASA Astrophysics Data System (ADS)

    Masalaite, A.; Remeikis, V.; Garbaras, A.; Dudoitis, V.; Ulevicius, V.; Ceburnis, D.

    2015-05-01

    Carbonaceous aerosol sources were investigated by measuring the stable carbon isotope ratio (δ13CTC) in size-segregated aerosol particles. The samples were collected with a micro-orifice uniform deposit impactor (MOUDI) in 11 size intervals ranging from 0.056 μm to 18 μm. The aerosol particle size distribution obtained from combined measurements with a scanning mobility particle sizer (SMPS; TSI 3936) and an aerosol particle sizer (APS; TSI 3321) is presented for comparison with MOUDI data. The analysis of δ13CTC values revealed that the total carbonaceous matter in size-segregated aerosol particles significantly varied from - 23.4 ± 0.1‰ in a coarse mode to - 30.1 ± 0.5‰ in a fine mode. A wide range of the δ13CTC values of size-segregated aerosol particles suggested various sources of aerosol particles contributing to carbonaceous particulate matter. Therefore, the source mixing equation was applied to verify the idea of mixing of two sources: continental non-fossil and fossil fuel combustion. The obtained δ13CTC value of aerosol particles originating from fossil fuel combustion was - 28.0 to - 28.1‰, while the non-fossil source δ13CTC value was in the range of - 25.0 to - 25.5‰. The two source mixing model applied to the size-segregated samples revealed that the fossil fuel combustion source contributed from 100% to 60% to the carbonaceous particulate matter in the fine mode range (Dp < 1 μm). Meanwhile, the second source, continental non-fossil, was the main contributor in the coarse fraction (Dp > 2 μm). The particle range from 0.5 to 2.0 μm was identified as a transition region where two sources almost equally contributed to carbonaceous particulate matter. The proposed mixing model offers an alternative method for determining major carbonaceous matter sources where radiocarbon analysis may lack the sensitivity (as in size-segregated samples).

  6. Calculation of aerosol optical properties under different assumptions on mixing state, refractive index, density and hygroscopicity: uncertainties and importance of representation of aerosol mixing state

    NASA Astrophysics Data System (ADS)

    Curci, Gabriele

    2015-04-01

    The calculation of aerosol optical properties from aerosol mass is a process subject to uncertainty related to necessary assumptions on the treatment of the chemical species mixing state, density, refractive index, and hygroscopic growth. We used the FlexAOD post-processing tool to calculate the optical properties (aerosol optical depth (AOD), single scattering albedo (SSA) and asymmetry parameter (g)) from chemistry-transport model aerosol profiles, using a wide range of assumptions on aerosol chemical and physical properties. We calculated that the most important factor of uncertainty is the assumption about the mixing state, for which we estimate an uncertainty of 30-35% on the simulated aerosol optical depth (AOD) and single scattering albedo (SSA). The choice of the core composition in the core-shell representation is of minor importance for calculation of AOD, while it is critical for the SSA. Other factors of uncertainty tested here have a maximum average impact of 10% each on calculated AOD, and an impact of a few percent on SSA and g. We then tested simple parameterizations of the aerosol mixing state, expressed as a function of the aerosol aging, and verified that they may be helpful in reducing the uncertainty when comparing simulations with AERONET retrievals.

  7. Representation and evaluation of aerosol mixing state in a climate model

    NASA Astrophysics Data System (ADS)

    Bauer, S. E.; Prather, K. A.; Ault, A. P.

    2011-12-01

    Aerosol particles in the atmosphere are composed out of multiple chemical species. The aerosol mixing state is an important aerosol property that will determine the interaction of aerosols with the climate system via radiative forcings and cloud activation. Through the introduction of aerosol microphysics into climate models, aerosol mixing state is by now taken into account to a certain extend in climate models, and evaluation of mixing state is the next challenge. Here we use data from the Aerosol Time of Flight Mass Spectrometer (ATOFMS) and compare the results to the GISS-modelE-MATRIX model, a global climate model including a detailed aerosol micro-physical scheme. We use data from various field campaigns probing, urban, rural and maritime air masses and compare those to climatological and nudged simulations for the years 2005 to 2009. ATOFMS provides information about the size distributions of several mixing state classes, including the chemical components of black and organic carbon, sulfates, dust and salts. MATRIX simulates 16 aerosol populations, which definitions are based on mixing state. We have grouped ATOFMS and MATRIX data into similar mixing state classes and compare the size resolved number concentrations against each other. As a first result we find that climatological simulations are rather difficult to evaluate with field data, and that nudged simulations give a much better agreement. However this is not just caused by the better fit of natural - meteorological driven - aerosol components, but also due to the interaction between meteorology and aerosol formation. The model seems to get the right amount of mixing state of black carbon material with sulfate and organic components, but seems to always overestimate the fraction of black carbon that is externally mixed. In order to understand this bias between model and the ATOFMS data, we will look into microphysical processes near emission sources and investigate the climate relevance of these sub

  8. Impact of Mixing State on Anthropogenic Aerosol Radiative Forcing and Associated Climate Response

    NASA Astrophysics Data System (ADS)

    Avramov, A.; Shin, H. J.; Wang, C.

    2014-12-01

    Atmospheric aerosols affect Earth's radiation balance directly by scattering and absorbing solar radiation and, indirectly, by changing the microphysical structure, lifetime and spatial extent of clouds. The aerosol mixing state to a large extent determines not only their optical properties (direct effect) but also their ability to serve as cloud condensation nuclei or ice nuclei (indirect effect). Results from previous research have highlighted the importance of the aerosol mixing assumptions in radiative forcing estimates in model simulations. Here we take a step further to analyze the differences in associated climate responses, using a multimodal, size- and mixing-dependent aerosol model (MARC) incorporated within the Community Earth System Model (CESM). The new model allows for a detailed representation of aerosol-radiation and aerosol-cloud interactions by including an improved treatment of aerosol mixing state and composition. First, we estimate and compare the magnitudes of direct and indirect forcing of anthropogenic aerosols under different mixing assumptions. We then carry out several century-long fully-coupled climate simulations designed to isolate the climate responses to direct and indirect forcings under the same aerosol mixing assumptions. In our analysis, we specifically focus on the following three climate response components: 1) cloud distribution and coverage; 2) precipitation amount and distribution; and 3) changes in circulation patterns.

  9. Thermohaline Mixing and Isotopic Ratios in AGB Stars

    NASA Astrophysics Data System (ADS)

    Stancliffe, R. J.

    2015-08-01

    I investigate the effects of thermohaline mixing on the isotopic ratios of asymptotic giant branch (AGB) stars. While thermohaline mixing has been shown to be an effective means of changing the surface composition of low-mass stars while they ascend the upper part of the giant branch, the effect of this mechanism on the AGB is almost negligible. The carbon isotopic ratio is barely affected during the earliest pulses, and as the 12C content increases due to third dredge-up this effect becomes seriously curtailed. This is because structural changes affect the relative locations of 3He-burning and the CNO cycle. While the isotopic ratios are barely affected by thermohaline mixing on the AGB, there is a substantial increase in the surface lithium abundance due to the action of this mechanism.

  10. Mixing ratios of carbon monoxide in the troposphere

    SciTech Connect

    Novelli, P.C.; Steele, L.P. ); Tans, P.P. )

    1992-12-20

    Carbon monoxide (CO) mixing ratios were measured in air samples collected weekly at eight locations. The air was collected as part of the CMDL/NOAA cooperative flask sampling program (Climate Monitoring and Diagnostics Laboratory, formerly Geophysical Monitoring for Climatic Change, Air Resources Laboratory/National Oceanic and Atmospheric Administration) at Point Barrow, Alaska, Niwot Ridge, Colorado, Mauna Loa and Cape Kumakahi, Hawaii, Guam, Marianas Islands, Christmas Island, Ascension Island and American Samoa. Half-liter or 3-L glass flasks fitted with glass piston stopcocks holding teflon O rings were used for sample collection. CO levels were determined within several weeks of collection using gas chromatography followed by mercuric oxide reduction detection, and mixing ratios were referenced against the CMDL/NOAA carbon monoxide standard scale. During the period of study (mid-1988 through December 1990) CO levels were greatest in the high latitudes of the northern hemisphere (mean mixing ratio from January 1989 to December 1990 at Point Barrow was approximately 154 ppb) and decreased towards the south (mean mixing ratio at Samoa over a similar period was 65 ppb). Mixing ratios varied seasonally, the amplitude of the seasonal cycle was greatest in the north and decreased to the south. Carbon monoxide levels were affected by both local and regional scale processes. The difference in CO levels between northern and southern latitudes also varied seasonally. The greatest difference in CO mixing ratios between Barrow and Samoa was observed during the northern winter (about 150 ppb). The smallest difference, 40 ppb, occurred during the austral winter. The annually averaged CO difference between 71[degrees]N and 14[degrees]S was approximately 90 ppb in both 1989 and 1990; the annually averaged interhemispheric gradient from 71[degrees]N to 41[degrees]S is estimated as approximately 95 ppb. 66 refs., 5 figs., 5 tabs.

  11. Aerosols in the study of convective acinar mixing

    NASA Technical Reports Server (NTRS)

    Darquenne, Chantal; Prisk, G. Kim

    2005-01-01

    Convective mixing (CM) refers to the different transport mechanisms except Brownian diffusion that irreversibly transfer inspired air into resident air and can be studied using aerosol bolus inhalations. This paper provides a review of the present understanding of how each of these mechanisms contributes to CM. Original data of the combined effect of stretch and fold and gravitational sedimentation on CM are also presented. Boli of 0.5 microm-diameter particles were inhaled at penetration volumes (V(p)) of 300 and 1200 ml in eight subjects. Inspiration was followed by a 10-s breath hold, during which small flow reversals (FR) were imposed, and expiration. There was no physiologically significant dependence in dispersion and deposition with increasing FR. The results were qualitatively similar to those obtained in a previous study in microgravity in which it was speculated that the phenomenon of stretch and fold occurred during the first breathing cycle without the need of any subsequent FR.

  12. Morphology and Optical Properties of Mixed Aerosol Particles

    NASA Astrophysics Data System (ADS)

    Fard, Mehrnoush M.; Krieger, Ulrich; Rudich, Yinon; Marcolli, Claudia; Peter, Thomas

    2016-04-01

    Experiments and modeling studies have shown that deliquesced aerosols can exist not only as one-phase system containing organics, inorganic salts and water, but often as two-phase systems consisting of a predominantly organic and a predominantly inorganic aqueous phase (1,2). Recent laboratory studies conducted with model mixtures representing tropospheric aerosols (1,2,3), secondary organic aerosol (SOA) from smog chamber experiments (4), and field measurements (5) suggest that liquid-liquid phase separations (LLPS) is indeed a common phenomenon in mixed organic/ inorganic particles. During LLPS, particles may adopt different morphologies mainly core-shell and partially engulfed. A core-shell configuration will have consequences for heterogeneous chemistry and hygroscopicity and as a result will alter the optical properties of the particles in particular for organic phases containing absorbing molecules, e.g. brown carbon. The primary objective of this project is to establish a method for investigating the morphology of mixed inorganic and absorbing organic compounds of atmospheric relevance and study their radiative properties before, during, and after phase transitions mainly during LLPS. This will be the first study looking into the radiative effect of LLPS in detail. Our ternary model system consist of ammonium sulfate (AS)/ Polyethylene Glycol (PEG)/ and water (H2O). Carminic acid (CA) was added as a proxy for an absorbing organic compound to the system. The behavior of single droplets of above ternary mixture was monitored during relative humidity (RH) cycles using optical microscopy. The same ternary mixture particle was levitated in an electrodynamic balance (EDB) and the change in its absorption properties was measured at varying RH. In addition, Mie-code modeling is used to predict the absorption efficiency of the same ternary system and the result will be compared with the data obtained from EDB experiment. We also intend to determine the occurrence of

  13. Influence of particle phase state on the hygroscopic behavior of mixed organic-inorganic aerosols

    NASA Astrophysics Data System (ADS)

    Hodas, N.; Zuend, A.; Mui, W.; Flagan, R. C.; Seinfeld, J. H.

    2014-12-01

    Recent work has demonstrated that organic and mixed organic-inorganic particles can exhibit multiple phase states depending on their chemical composition and on ambient conditions such as relative humidity (RH). To explore the extent to which water uptake varies with particle phase behavior, hygroscopic growth factors (HGFs) of nine laboratory-generated, organic and organic-inorganic aerosol systems with physical states ranging from well-mixed liquids, to phase-separated particles, to viscous liquids or semi-solids were measured with the Differential Aerosol Sizing and Hygroscopicity Spectrometer Probe at RH values ranging from 40-90%. Water-uptake measurements were accompanied by HGF and RH-dependent thermodynamic equilibrium calculations using the Aerosol Inorganic-Organic Mixtures Functional groups Activity Coefficients (AIOMFAC) model. In addition, AIOMFAC-predicted growth curves are compared to several simplified HGF modeling approaches: (1) representing particles as ideal, well-mixed liquids, (2) forcing a single phase, but accounting for non-ideal interactions through activity coefficient calculations, and (3) a Zdanovskii-Stokes-Robinson-like calculation in which complete separation between the inorganic and organic components is assumed at all RH values, with water-uptake treated separately in each of the individual phases. We observed variability in the characteristics of measured hygroscopic growth curves across aerosol systems with differing phase behaviors, with growth curves approaching smoother, more continuous water uptake with decreasing prevalence of liquid-liquid phase separation and increasing oxygen : carbon ratios of the organic aerosol components. We also observed indirect evidence for the dehydration-induced formation of highly viscous semi-solid phases and for kinetic limitations to the crystallization of ammonium sulfate at low RH for sucrose-containing particles. AIOMFAC-predicted growth curves are generally in good agreement with the HGF

  14. Influence of particle-phase state on the hygroscopic behavior of mixed organic-inorganic aerosols

    NASA Astrophysics Data System (ADS)

    Hodas, N.; Zuend, A.; Mui, W.; Flagan, R. C.; Seinfeld, J. H.

    2015-05-01

    Recent work has demonstrated that organic and mixed organic-inorganic particles can exhibit multiple phase states depending on their chemical composition and on ambient conditions such as relative humidity (RH). To explore the extent to which water uptake varies with particle-phase behavior, hygroscopic growth factors (HGFs) of nine laboratory-generated, organic and organic-inorganic aerosol systems with physical states ranging from well-mixed liquids to phase-separated particles to viscous liquids or semi-solids were measured with the Differential Aerosol Sizing and Hygroscopicity Spectrometer Probe at RH values ranging from 40 to 90%. Water-uptake measurements were accompanied by HGF and RH-dependent thermodynamic equilibrium calculations using the Aerosol Inorganic-Organic Mixtures Functional groups Activity Coefficients (AIOMFAC) model. In addition, AIOMFAC-predicted growth curves are compared to several simplified HGF modeling approaches: (1) representing particles as ideal, well-mixed liquids; (2) forcing a single phase but accounting for non-ideal interactions through activity coefficient calculations; and (3) a Zdanovskii-Stokes-Robinson-like calculation in which complete separation of the inorganic and organic components is assumed at all RH values, with water uptake treated separately in each of the individual phases. We observed variability in the characteristics of measured hygroscopic growth curves across aerosol systems with differing phase behaviors, with growth curves approaching smoother, more continuous water uptake with decreasing prevalence of liquid-liquid phase separation and increasing oxygen : carbon ratios of the organic aerosol components. We also observed indirect evidence for the dehydration-induced formation of highly viscous semi-solid phases and for kinetic limitations to the crystallization of ammonium sulfate at low RH for sucrose-containing particles. AIOMFAC-predicted growth curves are generally in good agreement with the HGF

  15. Long-range transport and mixing of aerosol sources during the 2013 North American biomass burning episode: analysis of multiple lidar observations in the western Mediterranean basin

    NASA Astrophysics Data System (ADS)

    Ancellet, Gerard; Pelon, Jacques; Totems, Julien; Chazette, Patrick; Bazureau, Ariane; Sicard, Michaël; Di Iorio, Tatiana; Dulac, Francois; Mallet, Marc

    2016-04-01

    Long-range transport of biomass burning (BB) aerosols between North America and the Mediterranean region took place in June 2013. A large number of ground-based and airborne lidar measurements were deployed in the western Mediterranean during the Chemistry-AeRosol Mediterranean EXperiment (ChArMEx) intensive observation period. A detailed analysis of the potential North American aerosol sources is conducted including the assessment of their transport to Europe using forward simulations of the FLEXPART Lagrangian particle dispersion model initialized using satellite observations by MODIS and CALIOP. The three-dimensional structure of the aerosol distribution in the ChArMEx domain observed by the ground-based lidars (Minorca, Barcelona and Lampedusa), a Falcon-20 aircraft flight and three CALIOP tracks, agrees very well with the model simulation of the three major sources considered in this work: Canadian and Colorado fires, a dust storm from western US and the contribution of Saharan dust streamers advected from the North Atlantic trade wind region into the westerlies region. Four aerosol types were identified using the optical properties of the observed aerosol layers (aerosol depolarization ratio, lidar ratio) and the transport model analysis of the contribution of each aerosol source: (i) pure BB layer, (ii) weakly dusty BB, (iii) significant mixture of BB and dust transported from the trade wind region, and (iv) the outflow of Saharan dust by the subtropical jet and not mixed with BB aerosol. The contribution of the Canadian fires is the major aerosol source during this episode while mixing of dust and BB is only significant at an altitude above 5 km. The mixing corresponds to a 20-30 % dust contribution in the total aerosol backscatter. The comparison with the MODIS aerosol optical depth horizontal distribution during this episode over the western Mediterranean Sea shows that the Canadian fire contributions were as large as the direct northward dust outflow

  16. Comparison of N2O5 mixing ratios during NO3Comp 2007 in SAPHIR

    NASA Astrophysics Data System (ADS)

    Fuchs, H.; Simpson, W. R.; Apodaca, R. L.; Brauers, T.; Cohen, R. C.; Crowley, J. N.; Dorn, H.-P.; Dubé, W. P.; Fry, J. L.; Häseler, R.; Kajii, Y.; Kiendler-Scharr, A.; Labazan, I.; Matsumoto, J.; Mentel, T. F.; Nakashima, Y.; Rohrer, F.; Rollins, A. W.; Schuster, G.; Tillmann, R.; Wahner, A.; Wooldridge, P. J.; Brown, S. S.

    2012-11-01

    N2O5 detection in the atmosphere has been accomplished using techniques which have been developed during the last decade. Most techniques use a heated inlet to thermally decompose N2O5 to NO3, which can be detected by either cavity based absorption at 662 nm or by laser-induced fluorescence. In summer 2007, a large set of instruments, which were capable of measuring NO3 mixing ratios, were simultaneously deployed in the atmosphere simulation chamber SAPHIR in Jülich, Germany. Some of these instruments measured N2O5 mixing ratios either simultaneously or alternatively. Experiments focused on the investigation of potential interferences from, e.g., water vapour or aerosol and on the investigation of the oxidation of biogenic volatile organic compounds by NO3. The comparison of N2O5 mixing ratios shows an excellent agreement between measurements of instruments applying different techniques (3 cavity ring-down (CRDS) instruments, 2 laser-induced fluorescence (LIF) instruments). Datasets are highly correlated as indicated by the square of the linear correlation coefficients, R2, which values were larger than 0.96 for the entire datasets. N2O5 mixing ratios well agree within the combined accuracy of measurements. Slopes of the linear regression range between 0.87 and 1.26 and intercepts are negligible. The most critical aspect of N2O5 measurements by cavity ring-down instruments is the determination of the inlet and filter transmission efficiency. Measurements here show that the N2O5 inlet transmission efficiency can decrease in the presence of high aerosol loads, and that frequent filter/inlet changing is necessary to quantitatively sample N2O5 in some environments. The analysis of data also demonstrates that a general correction for degrading filter transmission is not applicable for all conditions encountered during this campaign. Besides the effect of a gradual degradation of the inlet transmission efficiency aerosol exposure, no other interference for N2O5

  17. Comparison of N2O5 mixing ratios during NO3Comp 2007 in SAPHIR

    NASA Astrophysics Data System (ADS)

    Fuchs, H.; Simpson, W. R.; Apodaca, R. L.; Brauers, T.; Cohen, R. C.; Crowley, J. N.; Dorn, H.-P.; Dubé, W. P.; Fry, J. L.; Häseler, R.; Kajii, Y.; Kiendler-Scharr, A.; Labazan, I.; Matsumoto, J.; Mentel, T. F.; Nakashima, Y.; Rohrer, F.; Rollins, A. W.; Schuster, G.; Tillmann, R.; Wahner, A.; Wooldridge, P. J.; Brown, S. S.

    2012-07-01

    N2O5 detection in the atmosphere has been accomplished using techniques which have been developed during the last decade. Most techniques use a heated inlet to thermally decompose N2O5 to NO3, which can be detected by either cavity based absorption at 662 nm or by laser-induced fluorescence. In summer 2007, a large set of instruments, which were capable of measuring NO3 mixing ratios, were simultaneously deployed in the atmosphere simulation chamber SAPHIR in Jülich, Germany. Some of these instruments measured N2O5 mixing ratios either simultaneously or alternatively. Experiments focussed on the investigation of potential interferences from e.g. water vapor or aerosol and on the investigation of the oxidation of biogenic volatile organic compounds by NO3. The comparison of N2O5 mixing ratios shows an excellent agreement between measurements of instruments applying different techniques (3 cavity ring-down (CRDS) instruments, 2 laser-induced fluorescence (LIF) instruments). Data sets are highly correlated as indicated by the square of the linear correlation coefficients, R2, which values are larger than 0.96 for the entire data sets. N2O5 mixing ratios well agree within the combined accuracy of measurements. Slopes of the linear regression range between 0.87 and 1.26 and intercepts are negligible. The most critical aspect of N2O5 measurements by cavity ring-down instruments is the determination of the inlet and filter transmission efficiency. Measurements here show that the N2O5 inlet transmission efficiency can decrease in the presence of high aerosol loads, and that frequent filter/inlet changing is necessary to quantitatively sample N2O5 in some environments. The analysis of data also demonstrates that a general correction for degrading filter transmission is not applicable for all conditions encountered during this campaign. Besides the effect of a gradual degradation of the inlet transmission efficiency aerosol exposure, no other interference for N2O5

  18. Occultation determination of Neptune's oblateness and stratospheric methane mixing ratio

    NASA Technical Reports Server (NTRS)

    Lellouch, E.; Hubbard, W. B.; Sicardy, B.; Vilas, F.; Bouchet, P.

    1986-01-01

    The occultation of a star by Neptune on August 20, 1985 was observed at 2.2 micron wavelength with telescopes at the European Southern Observatory (ESO) and the Cerro Tololo Inter-American Observatory (CTIO). The detection of a 'central flash' midway between immersion and emersion has allowed the determination of Neptune's oblateness and the atmospheric extinction at 2.2 microns, which is related to the stratospheric methane mixing ratio. An oblateness of (2.08 +0.19 or -0.18) x 10 to the 2nd is found and, assuming a stratospheric temperature of 120 K, a value of 0.6 percent is inferred (with an uncertainty of a factor of 10) for the methane mixing ratio (CH4/H2) at 0.3 mbar. The latter value may indicate supersaturation of methane in Neptune's stratosphere.

  19. A simple method for estimation of coagulation efficiency in mixed aerosols. [environmental pollution control

    NASA Technical Reports Server (NTRS)

    Dimmick, R. L.; Boyd, A.; Wolochow, H.

    1975-01-01

    Aerosols of KBr and AgNO3 were mixed, exposed to light in a glass tube and collected in the dark. About 15% of the collected material was reduced to silver upon development. Thus, two aerosols of particles that react to form a photo-reducible compound can be used to measure coagulation efficiency.

  20. Selection Algorithm for the CALIPSO Lidar Aerosol Extinction-to-Backscatter Ratio

    NASA Technical Reports Server (NTRS)

    Omar, Ali H.; Winker, David M.; Vaughan, Mark A.

    2006-01-01

    The extinction-to-backscatter ratio (S(sub a)) is an important parameter used in the determination of the aerosol extinction and subsequently the optical depth from lidar backscatter measurements. We outline the algorithm used to determine Sa for the Cloud and Aerosol Lidar and Infrared Pathfinder Spaceborne Observations (CALIPSO) lidar. S(sub a) for the CALIPSO lidar will either be selected from a look-up table or calculated using the lidar measurements depending on the characteristics of aerosol layer. Whenever suitable lofted layers are encountered, S(sub a) is computed directly from the integrated backscatter and transmittance. In all other cases, the CALIPSO observables: the depolarization ratio, delta, the layer integrated attenuated backscatter, beta, and the mean layer total attenuated color ratio, gamma, together with the surface type, are used to aid in aerosol typing. Once the type is identified, a look-up-table developed primarily from worldwide observations, is used to determine the S(sub a) value. The CALIPSO aerosol models include desert dust, biomass burning, background, polluted continental, polluted dust, and marine aerosols.

  1. An Aerosol Extinction-to-Backscatter Ratio Database Derived from the NASA Micro-Pulse Lidar Network: Applications for Space-based Lidar Observations

    NASA Technical Reports Server (NTRS)

    Welton, Ellsworth J.; Campbell, James R.; Spinhime, James D.; Berkoff, Timothy A.; Holben, Brent; Tsay, Si-Chee; Bucholtz, Anthony

    2004-01-01

    Backscatter lidar signals are a function of both backscatter and extinction. Hence, these lidar observations alone cannot separate the two quantities. The aerosol extinction-to-backscatter ratio, S, is the key parameter required to accurately retrieve extinction and optical depth from backscatter lidar observations of aerosol layers. S is commonly defined as 4*pi divided by the product of the single scatter albedo and the phase function at 180-degree scattering angle. Values of S for different aerosol types are not well known, and are even more difficult to determine when aerosols become mixed. Here we present a new lidar-sunphotometer S database derived from Observations of the NASA Micro-Pulse Lidar Network (MPLNET). MPLNET is a growing worldwide network of eye-safe backscatter lidars co-located with sunphotometers in the NASA Aerosol Robotic Network (AERONET). Values of S for different aerosol species and geographic regions will be presented. A framework for constructing an S look-up table will be shown. Look-up tables of S are needed to calculate aerosol extinction and optical depth from space-based lidar observations in the absence of co-located AOD data. Applications for using the new S look-up table to reprocess aerosol products from NASA's Geoscience Laser Altimeter System (GLAS) will be discussed.

  2. The Effect of Aerosol Formation on Stable Isotopes Ratio in Titan's Atmosphere

    NASA Astrophysics Data System (ADS)

    Gautier, Thomas; Trainer, Melissa G.; Sebree, Joshua; Wold, Allison; Stern, Jennifer

    2016-10-01

    The formation of large amounts of aerosol in Titan atmosphere induces a significant sink for carbon and nitrogen in the atmosphere. Due to the high complexity of the chemistry leading to aerosol formation, there may be isotopic fractionation along the formation pathways of the aerosol. So far several stable isotopes have been measured in Titan atmosphere including the 13C/12C, 15N/14N and D/H ratios for different gaseous species. However, the fractionation effect of the aerosol formation and its impact on atmospheric stable isotope ratios has yet to be fully understood. Two experimental studies were recently published on the stable carbon [1] and nitrogen [1,2] isotope fractionation during aerosol formation in N2-CH4 reactant mixture. To better constrain the fractionation effect of aerosol formation on the Titan atmosphere we have measured the isotopic fractionation induced in laboratory aerosol analogues produced exploring the space of parameters that are expected to have an effect on fractionation processes. Parameters studied include pressure and temperature of aerosol formation and the reactant gas phase composition, including the standard "Titan" mixture of CH4/N2 as well as other trace species such as benzene (C6H6).[1] Sebree, J.A., Stern, J.C., Mandt, K.E., Domagal-Goldman, S.D., and Trainer, M.G.: C and N Fractionation of CH /N Mixtures during Photochemical Aerosol Formation: Relevance to Titan, (2016) Icarus 270:421-428[2] Kuga, M., Carrasco, N., Marty, B., Marrochi, Y., Bernard, S., Rigaudier, T., Fleury, B., Tissandier, L.: Nitrogen isotopic fractionation during abiotic synthesis of organic solid particles, (2014) EPSL 393:2-13

  3. Long range transport and mixing of aerosol sources during the 2013 North American biomass burning episode: analysis of multiple lidar observations in the Western Mediterranean basin

    NASA Astrophysics Data System (ADS)

    Ancellet, G.; Pelon, J.; Totems, J.; Chazette, P.; Bazureau, A.; Sicard, M.; Di Iorio, T.; Dulac, F.; Mallet, M.

    2015-11-01

    Long range transport of biomass burning (BB) aerosols between North America and the Mediterranean region took place in June 2013. A large number of ground based and airborne lidar measurements were deployed in the Western Mediterranean during the Chemistry-AeRosol Mediterranean EXperiment (ChArMEx) intensive observation period. A detailed analysis of the potential North American aerosol sources is conducted including the assessment of their transport to Europe using forward simulations of the FLEXPART Lagrangian particle dispersion model initialized using satellite observations by MODIS and CALIOP. The three dimensional structure of the aerosol distribution in the ChArMEx domain observed by the ground-based lidars (Menorca, Barcelona and Lampedusa), a Falcon-20 aircraft flight and three CALIOP tracks, agree very well with the model simulation of the three major sources considered in this work: Canadian and Colorado fires, a dust storm from Western US and the contribution of Saharan dust streamers advected from the North Atlantic trade wind region into the Westerlies region. Four aerosol types were identified using the optical properties of the observed aerosol layers (aerosol depolarization ratio, lidar ratio) and the transport model analysis of the contribution of each aerosol source: (I) pure BB layer, (II) weakly dusty BB, (III) significant mixture of BB and dust transported from the trade wind region (IV) the outflow of Saharan dust by the subtropical jet and not mixed with BB aerosol. The contribution of the Canadian fires is the major aerosol source during this episode while mixing of dust and BB is only significant at altitude above 5 km. The mixing corresponds to a 20-30 % dust contribution in the total aerosol backscatter. The comparison with the MODIS AOD horizontal distribution during this episode over the Western Mediterranean sea shows that the Canadian fires contribution were as large as the direct northward dust outflow from Sahara.

  4. Meteorological factors affecting lower tropospheric ozone mixing ratios in Bangkok, Thailand

    NASA Astrophysics Data System (ADS)

    Janjai, S.; Buntoung, S.; Nunez, M.; Chiwpreecha, K.; Pattarapanitchai, S.

    2016-09-01

    This paper examines the influence of meteorological conditions in ozone mixing ratio measured at the Thai Meteorological Department (TMD) in Bangkok, Thailand. In addition to surface wind speed and direction, surface ozone concentrations, ozonesondes and CALIPSO Lidar images were collected during the study period extending from 01/01/2014 to 30/04/2015. Surface ozone concentrations show a strong seasonality, with maximum in the dry months of December to April and minimum during the wet southwest (SW) monsoon period extending from May to October. High ozone concentrations are related to biomass burning in the northeast highland regions of the country and neighboring Myanmar and southern China. These precursors travel in a southerly direction towards Bangkok in a well-defined aerosol layer which may be at ground level or at elevated heights. The growth of the daytime mixed layer scavenges some of the upper level aerosols, although local maxima in ozone concentrations at 1-2 km are a frequent feature at Bangkok. There is an evidence of fumigation in the Gulf of Thailand and a return flow via the southerly sea breezes.

  5. Surrogate/spent fuel sabotage : aerosol ratio test program and Phase 2 test results.

    SciTech Connect

    Borek, Theodore Thaddeus III; Thompson, N. Slater; Sorenson, Ken Bryce; Hibbs, R.S.; Nolte, Oliver; Molecke, Martin Alan; Autrusson, Bruno; Young, F. I.; Koch, Wolfgang; Brochard, Didier; Pretzsch, Gunter Guido; Lange, Florentin

    2004-05-01

    A multinational test program is in progress to quantify the aerosol particulates produced when a high energy density device, HEDD, impacts surrogate material and actual spent fuel test rodlets. This program provides needed data that are relevant to some sabotage scenarios in relation to spent fuel transport and storage casks, and associated risk assessments; the program also provides significant political benefits in international cooperation. We are quantifying the spent fuel ratio, SFR, the ratio of the aerosol particles released from HEDD-impacted actual spent fuel to the aerosol particles produced from surrogate materials, measured under closely matched test conditions. In addition, we are measuring the amounts, nuclide content, size distribution of the released aerosol materials, and enhanced sorption of volatile fission product nuclides onto specific aerosol particle size fractions. These data are crucial for predicting radiological impacts. This document includes a thorough description of the test program, including the current, detailed test plan, concept and design, plus a description of all test components, and requirements for future components and related nuclear facility needs. It also serves as a program status report as of the end of FY 2003. All available test results, observations, and analyses - primarily for surrogate material Phase 2 tests using cerium oxide sintered ceramic pellets are included. This spent fuel sabotage - aerosol test program is coordinated with the international Working Group for Sabotage Concerns of Transport and Storage Casks, WGSTSC, and supported by both the U.S. Department of Energy and Nuclear Regulatory Commission.

  6. Black carbon mixing state impacts on cloud microphysical properties: effects of aerosol plume and environmental conditions

    SciTech Connect

    Ching, Ping Pui; Riemer, Nicole; West, Matthew

    2016-05-27

    Black carbon (BC) is usually mixed with other aerosol species within individual aerosol particles. This mixture, along with the particles' size and morphology, determines the particles' optical and cloud condensation nuclei properties, and hence black carbon's climate impacts. In this study the particle-resolved aerosol model PartMC-MOSAIC was used to quantify the importance of black carbon mixing state for predicting cloud microphysical quantities. Based on a set of about 100 cloud parcel simulations a process level analysis framework was developed to attribute the response in cloud microphysical properties to changes in the underlying aerosol population ("plume effect") and the cloud parcel cooling rate ("parcel effect"). It shows that the response of cloud droplet number concentration to changes in BC emissions depends on the BC mixing state. When the aerosol population contains mainly aged BC particles an increase in BC emission results in increasing cloud droplet number concentrations ("additive effect"). In contrast, when the aerosol population contains mainly fresh BC particles they act as sinks for condensable gaseous species, resulting in a decrease in cloud droplet number concentration as BC emissions are increased ("competition effect"). Additionally, we quantified the error in cloud microphysical quantities when neglecting the information on BC mixing state, which is often done in aerosol models. The errors ranged from -12% to +45% for the cloud droplet number fraction, from 0% to +1022% for the nucleation-scavenged black carbon (BC) mass fraction, from -12% to +4% for the effective radius, and from -30% to +60% for the relative dispersion.

  7. Stratospheric HBr mixing ratio obtained from far infrared emission spectra

    NASA Technical Reports Server (NTRS)

    Park, J. H.; Carli, B.; Barbis, A.

    1989-01-01

    Emission features of HBr isotopes have been identified in high-resolution FIR emission spectra obtained with a balloon-borne Fourier-transform spectrometer in the spring of 1979 at 32 deg N latitude. When six single-scan spectra at a zenith angle of 93.2 deg were averaged, two features of HBr isotopes at 50.054 and 50.069/cm were obtained with a signal-to-noise ratio of 2.5. The volume mixing ratio retrieved from the average spectrum is 2.0 x 10 to the -11th, which is assumed to be constant above 28 km, with an uncertainty of 35 percent. This stratospheric amount of HBr is about the same as the current level of tropospheric organic bromine compounds, 25 pptv. Thus HBr could be the major stratospheric bromine species.

  8. Stratospheric HBr mixing ratio obtained from far infrared emission spectra

    SciTech Connect

    Park, J.H. ); Carli, B. ); Barbis, A. )

    1989-08-01

    Emission features of HBr isotopes have been identified in high-resolution far-infrared emission spectra obtained with a balloon-born Fourier transform spectrometer in the spring of 1979 at 32{degree}N latitude. When six single-scan spectra at a zenith angle of 93.2{degree} were averaged, two features of HBr isotopes at 50.054 and 50.069 cm{sup {minus}1} were obtained with a signal-to-noise ratio of 2.5. The volume mixing ratio retrieved from the average spectrum is 2.0 {times} 10{sub {minus}11}, which is assumed to be constant above 28 km, with an uncertainty of 35%. This stratospheric amount of HBr is about the same as the current level of tropospheric organic bromine compounds, 25 pptv. Thus, HBr could be the major stratospheric bromine species.

  9. The Impact of Aerosol Particle Mixing State on the Hygroscopicity of Sea Spray Aerosol.

    PubMed

    Schill, Steven R; Collins, Douglas B; Lee, Christopher; Morris, Holly S; Novak, Gordon A; Prather, Kimberly A; Quinn, Patricia K; Sultana, Camille M; Tivanski, Alexei V; Zimmermann, Kathryn; Cappa, Christopher D; Bertram, Timothy H

    2015-06-24

    Aerosol particles influence global climate by determining cloud droplet number concentrations, brightness, and lifetime. Primary aerosol particles, such as those produced from breaking waves in the ocean, display large particle-particle variability in chemical composition, morphology, and physical phase state, all of which affect the ability of individual particles to accommodate water and grow into cloud droplets. Despite such diversity in molecular composition, there is a paucity of methods available to assess how particle-particle variability in chemistry translates to corresponding differences in aerosol hygroscopicity. Here, an approach has been developed that allows for characterization of the distribution of aerosol hygroscopicity within a chemically complex population of atmospheric particles. This methodology, when applied to the interpretation of nascent sea spray aerosol, provides a quantitative framework for connecting results obtained using molecular mimics generated in the laboratory with chemically complex ambient aerosol. We show that nascent sea spray aerosol, generated in situ in the Atlantic Ocean, displays a broad distribution of particle hygroscopicities, indicative of a correspondingly broad distribution of particle chemical compositions. Molecular mimics of sea spray aerosol organic material were used in the laboratory to assess the volume fractions and molecular functionality required to suppress sea spray aerosol hygroscopicity to the extent indicated by field observations. We show that proper accounting for the distribution and diversity in particle hygroscopicity and composition are important to the assessment of particle impacts on clouds and global climate.

  10. Quantification of black carbon mixing state from traffic: Implications for aerosol optical properties

    SciTech Connect

    Willis, Megan D.; Healy, Robert M.; Riemer, Nicole; West, Matthew; Wang, Jon M.; Jeong, Cheol -Heon; Wenger, John C.; Evans, Greg J.; Abbatt, Jonathan P. D.; Lee, Alex K. Y.

    2016-04-14

    The climatic impacts of black carbon (BC) aerosol, an important absorber of solar radiation in the atmosphere, remain poorly constrained and are intimately related to its particle-scale physical and chemical properties. Using particle-resolved modelling informed by quantitative measurements from a soot-particle aerosol mass spectrometer, we confirm that the mixing state (the distribution of co-emitted aerosol amongst fresh BC-containing particles) at the time of emission significantly affects BC-aerosol optical properties even after a day of atmospheric processing. Both single particle and ensemble aerosol mass spectrometry observations indicate that BC near the point of emission co-exists with hydrocarbon-like organic aerosol (HOA) in two distinct particle types: HOA-rich and BC-rich particles. The average mass fraction of black carbon in HOA-rich and BC-rich particle classes was  < 0.1 and 0.8, respectively. Notably, approximately 90 % of BC mass resides in BC-rich particles. This new measurement capability provides quantitative insight into the physical and chemical nature of BC-containing particles and is used to drive a particle-resolved aerosol box model. Lastly, significant differences in calculated single scattering albedo (an increase of 0.1) arise from accurate treatment of initial particle mixing state as compared to the assumption of uniform aerosol composition at the point of BC injection into the atmosphere.

  11. Quantification of black carbon mixing state from traffic: Implications for aerosol optical properties

    DOE PAGES

    Willis, Megan D.; Healy, Robert M.; Riemer, Nicole; ...

    2016-04-14

    The climatic impacts of black carbon (BC) aerosol, an important absorber of solar radiation in the atmosphere, remain poorly constrained and are intimately related to its particle-scale physical and chemical properties. Using particle-resolved modelling informed by quantitative measurements from a soot-particle aerosol mass spectrometer, we confirm that the mixing state (the distribution of co-emitted aerosol amongst fresh BC-containing particles) at the time of emission significantly affects BC-aerosol optical properties even after a day of atmospheric processing. Both single particle and ensemble aerosol mass spectrometry observations indicate that BC near the point of emission co-exists with hydrocarbon-like organic aerosol (HOA) inmore » two distinct particle types: HOA-rich and BC-rich particles. The average mass fraction of black carbon in HOA-rich and BC-rich particle classes was  < 0.1 and 0.8, respectively. Notably, approximately 90 % of BC mass resides in BC-rich particles. This new measurement capability provides quantitative insight into the physical and chemical nature of BC-containing particles and is used to drive a particle-resolved aerosol box model. Lastly, significant differences in calculated single scattering albedo (an increase of 0.1) arise from accurate treatment of initial particle mixing state as compared to the assumption of uniform aerosol composition at the point of BC injection into the atmosphere.« less

  12. Multipole mixing ratios and substate populations in Rn-219

    NASA Astrophysics Data System (ADS)

    Jones, G. D.

    2016-08-01

    Historical alpha-gamma angular correlation data for the decay of 223Ra into excited states of 219Rn have been analysed, using the correct spins of the states involved, for the first time. The analyses produced multipole mixing ratios (E2/M1) of δ (144)=-0.11\\+/- 0.03, δ (154)=0, δ (158)=-0.205\\+/- 0.018 and δ (269)=-0.149\\+/- 0.004 where the nominal transition energies, in keV, are given in brackets. These values are consistent with published values obtained from internal conversion electron spectroscopy. It is also found that δ (324)=0 and δ (338)=-0.235\\+/- 0.030 (where both values differ from current tabulations) and that the sign of the multipole mixing ratio for the 122 keV transition is negative. The 158, 269 and 338 keV states are found to be aligned with high population of M=+/- 3/2 substates and the 127 keV state is believed to have undergone spin relaxation.

  13. Spent fuel sabotage aerosol ratio program : FY 2004 test and data summary.

    SciTech Connect

    Brucher, Wenzel; Koch, Wolfgang; Pretzsch, Gunter Guido; Loiseau, Olivier; Mo, Tin; Billone, Michael C.; Autrusson, Bruno A.; Young, F. I.; Coats, Richard Lee; Burtseva, Tatiana; Luna, Robert Earl; Dickey, Roy R.; Sorenson, Ken Bryce; Nolte, Oliver; Thompson, Nancy Slater; Hibbs, Russell S.; Gregson, Michael Warren; Lange, Florentin; Molecke, Martin Alan; Tsai, Han-Chung

    2005-07-01

    This multinational, multi-phase spent fuel sabotage test program is quantifying the aerosol particles produced when the products of a high energy density device (HEDD) interact with and explosively particulate test rodlets that contain pellets of either surrogate materials or actual spent fuel. This program has been underway for several years. This program provides data that are relevant to some sabotage scenarios in relation to spent fuel transport and storage casks, and associated risk assessments. The program also provides significant technical and political benefits in international cooperation. We are quantifying the Spent Fuel Ratio (SFR), the ratio of the aerosol particles released from HEDD-impacted actual spent fuel to the aerosol particles produced from surrogate materials, measured under closely matched test conditions, in a contained test chamber. In addition, we are measuring the amounts, nuclide content, size distribution of the released aerosol materials, and enhanced sorption of volatile fission product nuclides onto specific aerosol particle size fractions. These data are the input for follow-on modeling studies to quantify respirable hazards, associated radiological risk assessments, vulnerability assessments, and potential cask physical protection design modifications. This document includes an updated description of the test program and test components for all work and plans made, or revised, during FY 2004. It also serves as a program status report as of the end of FY 2004. All available test results, observations, and aerosol analyses plus interpretations--primarily for surrogate material Phase 2 tests, series 2/5A through 2/9B, using cerium oxide sintered ceramic pellets are included. Advanced plans and progress are described for upcoming tests with unirradiated, depleted uranium oxide and actual spent fuel test rodlets. This spent fuel sabotage--aerosol test program is coordinated with the international Working Group for Sabotage Concerns of

  14. Aerosol organic carbon to black carbon ratios: Analysis ofpublished data and implications for climate forcing

    SciTech Connect

    Novakov, T.; Menon, S.; Kirchstetter, T.W.; Koch, D.; Hansen, J.E.

    2005-07-11

    Measurements of organic carbon (OC) and black carbon (BC)concentrations over a variety of locations worldwide, have been analyzed to infer the spatial distributions of the ratios of OC to BC. Since these ratios determine the relative amounts of scattering and absorption, they are often used to estimate the radiative forcing due to aerosols. An artifact in the protocol for filter measurements of OC has led to widespread overestimates of the ratio of OC to BC in atmospheric aerosols. We developed a criterion to correct for this artifact and analyze corrected OC to BC ratios. The OC to BC ratios, ranging from 1.3to 2.4, appear relatively constant and are generally unaffected by seasonality, sources or technology changes, at the locations considered here. The ratios compare well with emission inventories over Europe and China but are a factor of two lower in other regions. The reduced estimate for OC/BC in aerosols strengthens the argument that reduction of soot emissions maybe a useful approach to slow global warming.

  15. Passive scalar mixing: Analytic study of time scale ratio, variance, and mix rate

    NASA Astrophysics Data System (ADS)

    Ristorcelli, J. R.

    2006-07-01

    Some very reasonable approximations, consistent with numerical and experimental evidence, were applied to the skewness and palinstrophy coefficients in the dissipation equations to produce a simple closed moment model for mixing. Such a model, first suggested on the grounds of a Taylor microscale self-similarity of the scalar field, was studied numerically by Gonzalez and Fall ["The approach to self-preservation of scalar fluctuation decay in isotropic turbulence," Phys. Fluids 10, 654 (1998)]. Here, in a somewhat old fashioned and physically meaningful style, analytic solutions to the four coupled nonlinear moment equations for mixing by decaying and forced stationary turbulence, are given. Analytic expressions for the variance ⟨c2⟩, the mixing rate ɛc, and the time scale ratio r(t ) are derived and compared in different mixing situations. The solutions show the sensitive dependence on the initial relative length ratio as studied experimentally by Warhaft and Lumley ["An experimental study of the decay of temperature fluctuations in grid-generated turbulence," J. Fluid Mech. 88, 659 (1978)], and simulated by Eswaran and Pope ["Direct numerical simulation of the turbulent mixing of a passive scalar," Phys. Fluids 31, 506 (1988)]. The length scale ratio saturation effect predicted by Durbin ["Analysis of the decay of temperature fluctuations in isotropic turbulence," Phys. Fluids 25, 1328 (1982)], resolving the apparent contradiction with the results of Sreenivasan, Tavoularis, and Corrsin ["Temperature fluctuations and scales in grid generated turbulence," J. Fluid Mech. 100, 597 (1980)] is predicted. For stationary turbulence the solutions indicate, in contradistinction to the power law "stirring" result predicted by a stochastic Lagrangian analysis, that the mixing is asymptotically exponential as shown in the phenomenological analysis of Corrsin ["The isotropic turbulent mixer," AIChE J. 10, 870 (1964)]. That the time scale ratio solution also depends on

  16. Elemental ratio measurements of organic compounds using aerosol mass spectrometry: characterization, improved calibration, and implications

    NASA Astrophysics Data System (ADS)

    Canagaratna, M. R.; Jimenez, J. L.; Kroll, J. H.; Chen, Q.; Kessler, S. H.; Massoli, P.; Hildebrandt Ruiz, L.; Fortner, E.; Williams, L. R.; Wilson, K. R.; Surratt, J. D.; Donahue, N. M.; Jayne, J. T.; Worsnop, D. R.

    2015-01-01

    Elemental compositions of organic aerosol (OA) particles provide useful constraints on OA sources, chemical evolution, and effects. The Aerodyne high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS) is widely used to measure OA elemental composition. This study evaluates AMS measurements of atomic oxygen-to-carbon (O : C), hydrogen-to-carbon (H : C), and organic mass-to-organic carbon (OM : OC) ratios, and of carbon oxidation state (OS C) for a vastly expanded laboratory data set of multifunctional oxidized OA standards. For the expanded standard data set, the method introduced by Aiken et al. (2008), which uses experimentally measured ion intensities at all ions to determine elemental ratios (referred to here as "Aiken-Explicit"), reproduces known O : C and H : C ratio values within 20% (average absolute value of relative errors) and 12%, respectively. The more commonly used method, which uses empirically estimated H2O+ and CO+ ion intensities to avoid gas phase air interferences at these ions (referred to here as "Aiken-Ambient"), reproduces O : C and H : C of multifunctional oxidized species within 28 and 14% of known values. The values from the latter method are systematically biased low, however, with larger biases observed for alcohols and simple diacids. A detailed examination of the H2O+, CO+, and CO2+ fragments in the high-resolution mass spectra of the standard compounds indicates that the Aiken-Ambient method underestimates the CO+ and especially H2O+ produced from many oxidized species. Combined AMS-vacuum ultraviolet (VUV) ionization measurements indicate that these ions are produced by dehydration and decarboxylation on the AMS vaporizer (usually operated at 600 °C). Thermal decomposition is observed to be efficient at vaporizer temperatures down to 200 °C. These results are used together to develop an "Improved-Ambient" elemental analysis method for AMS spectra measured in air

  17. Elemental ratio measurements of organic compounds using aerosol mass spectrometry: characterization, improved calibration, and implications

    DOE PAGES

    Canagaratna, M. R.; Jimenez, J. L.; Kroll, J. H.; ...

    2015-01-12

    Elemental compositions of organic aerosol (OA) particles provide useful constraints on OA sources, chemical evolution, and effects. The Aerodyne high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS) is widely used to measure OA elemental composition. This study evaluates AMS measurements of atomic oxygen-to-carbon (O : C), hydrogen-to-carbon (H : C), and organic mass-to-organic carbon (OM : OC) ratios, and of carbon oxidation state (OS C) for a vastly expanded laboratory data set of multifunctional oxidized OA standards. For the expanded standard data set, the method introduced by Aiken et al. (2008), which uses experimentally measured ion intensities at all ions to determinemore » elemental ratios (referred to here as "Aiken-Explicit"), reproduces known O : C and H : C ratio values within 20% (average absolute value of relative errors) and 12%, respectively. The more commonly used method, which uses empirically estimated H2O+ and CO+ ion intensities to avoid gas phase air interferences at these ions (referred to here as "Aiken-Ambient"), reproduces O : C and H : C of multifunctional oxidized species within 28 and 14% of known values. The values from the latter method are systematically biased low, however, with larger biases observed for alcohols and simple diacids. A detailed examination of the H2O+, CO+, and CO2+ fragments in the high-resolution mass spectra of the standard compounds indicates that the Aiken-Ambient method underestimates the CO+ and especially H2O+ produced from many oxidized species. Combined AMS–vacuum ultraviolet (VUV) ionization measurements indicate that these ions are produced by dehydration and decarboxylation on the AMS vaporizer (usually operated at 600 °C). Thermal decomposition is observed to be efficient at vaporizer temperatures down to 200 °C. These results are used together to develop an "Improved-Ambient" elemental analysis method for AMS spectra measured in air. The Improved-Ambient method uses specific ion

  18. Aerosol mixing state, hygroscopic growth and cloud activation efficiency during MIRAGE 2006

    NASA Astrophysics Data System (ADS)

    Lance, S.; Raatikainen, T.; Onasch, T. B.; Worsnop, D. R.; Yu, X.-Y.; Alexander, M. L.; Stolzenburg, M. R.; McMurry, P. H.; Smith, J. N.; Nenes, A.

    2013-05-01

    Observations of aerosol hygroscopic growth and CCN activation spectra for submicron particles are reported for the T1 ground site outside of Mexico City during the MIRAGE 2006 campaign. κ-Köhler theory is used to evaluate the characteristic hygroscopicity parameter, κ*, for the CCN active aerosol population using both size-resolved HTMDA and size-resolved CCNc measurements. Organic mass fractions (forg) are evaluated from size-resolved aerosol mass spectrometer (AMS) measurements, from which predictions of the hygroscopicity parameter are compared against κ*. Strong diurnal changes in aerosol water uptake parameters and aerosol composition are observed. We find that new particle formation (NPF) events are correlated with an increased κ* and CCN-active fraction during the daytime, with greater impact on smaller particles. During NPF events, the number concentration of 40 nm particles acting as CCN at 0.51% ± 0.06% supersaturation can surpass by more than a factor of two the corresponding concentrations of 100 nm particles. We also find that at 06:00-08:00 LT throughout the campaign, fresh traffic emissions result in substantial changes to the chemical distribution of the aerosol, with on average 65% externally mixed fraction for 40 nm particles and 30% externally mixed fraction for 100 nm particles, whereas at midday nearly all particles of both sizes can be described as "internally mixed". Average activation spectra and growth factor distributions are analyzed for different time periods characterizing the daytime (with and without NPF events), the early morning "rush hour" and the entire campaign. We show that κ* derived from CCNc measurements decreases as a function of size during all time periods, while the CCN-active fraction increases as a function of size. Size-resolved AMS measurements do not predict the observed trend for κ* versus particle size, which can be attributed to unresolved mixing state and the presence of refractory material not measured

  19. Effective Lidar Ratios of Dense Dust Aerosol Layers over North Africa Observed by the CALIPSO Lidar

    NASA Astrophysics Data System (ADS)

    Liu, Z.; Winker, D. M.; Omar, A. H.; Vaughan, M.; Trepte, C. R.; Hu, Y.; Hostetler, C. A.; Sun, W.; Lin, B.

    2009-12-01

    The Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observation (CALIPSO) satellite, a joint US and French mission, was launched three years ago to provide new insight into the role that clouds and aerosols play in regulating Earth's weather, climate, and air quality. A key instrument on board the CALIPSO payload is a two-wavelength, polarization-sensitive backscatter lidar. With its capabilities of depolarization ratio measurement and high resolution profiling, the CALIPSO lidar provides a unique opportunity to study the dust aerosol globally. Currently, a cloud and aerosol discrimination (CAD) algorithm that incorporates five-dimensional probability distribution function (5D-PDF) is being developed for implementation in future data releases. This new 5D-PDF approach allows nearly unambiguous identification of dense dust layers over/near their source regions and therefore enables the study of these layers using a large amount of the CALIPSO data. Lidar ratio (i.e., extinction-to-backscatter ratio) is an intrinsic optical property of aerosols and a key parameter necessary in the lidar signal inversion to retrieve profiles of aerosol extinction and backscatter coefficients, which are two primary products of the CALIPSO level 2 data. This parameter is usually selected in the CALIPSO lidar level 2 data processing based on the aerosol type identified. (Six types of aerosols have been modeled: dust, polluted dust, marine, continental, polluted continental, and smoke.) As more data is being collected by the CALIPSO lidar, validation studies with the CALIPSO measurements are being performed and are now becoming available. For opaque dust layers, the effective lidar ratio (the product of lidar ratio and multiple scattering factor) can be determined easily from integrated attenuated backscatter over the layer top and apparent base. We have performed an extensive analysis based on the first two and a half years (June 2006 - December 2008) of the CALIPSO lidar nighttime

  20. Elemental ratio measurements of organic compounds using aerosol mass spectrometry: characterization, improved calibration, and implications

    DOE PAGES

    Canagaratna, M. R.; Jimenez, J. L.; Kroll, J. H.; ...

    2014-07-31

    Elemental compositions of organic aerosol (OA) particles provide useful constraints on OA sources, chemical evolution, and effects. The Aerodyne high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS) is widely used to measure OA elemental composition. This study evaluates AMS measurements of atomic oxygen-to-carbon (O : C), hydrogen-to-carbon (H : C), organic mass-to-organic carbon (OM : OC), and carbon oxidation state (OSC) for a vastly expanded laboratory dataset of multifunctional oxidized OA standards. For the expanded standard dataset, the "Aiken-Explicit" method (Aiken et al., 2008), which uses experimentally measured ion intensities at all ions to determine elemental ratios, reproduces known molecular O :more » C and H : C ratio values within 20% (average absolute value of relative errors) and 12% respectively. The more commonly used "Aiken-Ambient" method, which uses empirically estimated H2O+ and CO+ ion intensities to avoid gas phase air interferences at these ions, reproduces O : C and H : C of multifunctional oxidized species within 28% and 14% of known values. These values are systematically biased low, however, with larger biases observed for alcohols and simple diacids. A detailed examination of the H2O+, CO+, and CO2+ fragments in the high-resolution mass spectra of the standard compounds indicates that the Aiken-Ambient method underestimates the CO+ and H2O+ produced from many oxidized species. Combined AMS-vacuum ultraviolet (VUV) ionization measurements indicate that these ions are produced by dehydration and decarboxylation on the AMS vaporizer (usually operated at 600 °C). Thermal decomposition is observed to be efficient at vaporizer temperatures down to 200 °C. These results are used together to develop an "Improved-Ambient" elemental analysis method for AMS spectra measured in air. The Improved-Ambient method reduces the systematic biases and reproduces O : C (H : C) ratios of individual oxidized standards within 28% (13

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

    SciTech Connect

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

    2010-03-15

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

  2. Influence of the external mixing state of atmospheric aerosol on derived CCN number concentrations

    NASA Astrophysics Data System (ADS)

    Wex, H.; McFiggans, G.; Henning, S.; Stratmann, F.

    2010-05-01

    We derived the range of particle hygroscopicities ($\\kappa$) that occurs in the atmosphere, based on literature data of measured hygroscopic growth or based on chemical composition. The derived $\\kappa$-values show that the atmospheric aerosol often is an external mixture with respect to hygroscopicity. Mean $\\kappa$ were derived for urban, rural, and marine aerosols for the different hygroscopic modes. Using these $\\kappa$ and exemplary particle number size distributions for the different aerosols, the number concentration of cloud condensation nuclei (NCCN) was derived for two cases, (1) accounting for the less hygroscopic fraction of particles and (2) assuming all particles to have $\\kappa$ of the more hygroscopic mode. NCCN derived from measured particle hygroscopicity is overestimated for case (2). Overestimation of NCCN is largest for fresh continental aerosol and less pronounced for marine aerosol. With $\\kappa$ derived from bulk aerosol composition data, only the hygroscopicity of more soluble aerosol particles is captured. Bulk or even size-resolved composition data will be insufficient to predict NCCN under many conditions unless independent information about particle mixing state is available.

  3. Venus cloud properties: Infrared opacity and mass mixing ratio

    NASA Technical Reports Server (NTRS)

    Samuelson, R. E.; Hanel, R. A.; Herath, L. W.; Kunde, V. G.; Maguire, W. C.

    1974-01-01

    By using the Mariner 5 temperature profile and a homogeneous cloud model, and assuming that CO2 and cloud particles are the only opacity sources, the wavelength dependence of the Venus cloud opacity is inferred from the infrared spectrum of the planet between 450 and 1250/cm. Justification for applying the homogeneous cloud model is found in the fact that numerous polarization and infrared data are mutually consistent within the framework of such a model; on the other hand, dense cloud models are not satisfactory. Volume extinction coefficients varying from 0.000005 to 0.000015/cm depending on the wavelength, are determined at the tropopause level of 6110 km. By using all available data, a cloud mass mixing ratio of approximately 0.000005 and a particle concentration of about 900 particles per cu cm at this level are also inferred. The derived cloud opacity compares favorably with that expected for a haze of droplets of a 75% aqueous solution of sulfuric acid.

  4. Parameterizing radiative transfer to convert MAX-DOAS dSCDs into near-surface box-averaged mixing ratios

    NASA Astrophysics Data System (ADS)

    Sinreich, R.; Merten, A.; Molina, L.; Volkamer, R.

    2013-06-01

    We present a novel parameterization method to convert multi-axis differential optical absorption spectroscopy (MAX-DOAS) differential slant column densities (dSCDs) into near-surface box-averaged volume mixing ratios. The approach is applicable inside the planetary boundary layer under conditions with significant aerosol load, and builds on the increased sensitivity of MAX-DOAS near the instrument altitude. It parameterizes radiative transfer model calculations and significantly reduces the computational effort, while retrieving ~ 1 degree of freedom. The biggest benefit of this method is that the retrieval of an aerosol profile, which usually is necessary for deriving a trace gas concentration from MAX-DOAS dSCDs, is not needed. The method is applied to NO2 MAX-DOAS dSCDs recorded during the Mexico City Metropolitan Area 2006 (MCMA-2006) measurement campaign. The retrieved volume mixing ratios of two elevation angles (1° and 3°) are compared to volume mixing ratios measured by two long-path (LP)-DOAS instruments located at the same site. Measurements are found to agree well during times when vertical mixing is expected to be strong. However, inhomogeneities in the air mass above Mexico City can be detected by exploiting the different horizontal and vertical dimensions probed by the MAX-DOAS and LP-DOAS instruments. In particular, a vertical gradient in NO2 close to the ground can be observed in the afternoon, and is attributed to reduced mixing coupled with near-surface emission inside street canyons. The existence of a vertical gradient in the lower 250 m during parts of the day shows the general challenge of sampling the boundary layer in a representative way, and emphasizes the need of vertically resolved measurements.

  5. Quantification of Feedbacks in Aerosol-Cloud-Precipitation Interactions of Mixed-Phase Clouds

    NASA Astrophysics Data System (ADS)

    Glassmeier, F.; Herger, N.; Ramelli, F.; Lohmann, U.

    2014-12-01

    The notion of clouds as buffered or resilient systems implies that generalized feedback processes unaccounted for in climate simulations may lead to an overestimation of the effective radiative forcing due to aerosol-cloud interactions, i.e. cloud lifetime effects. In this contribution, we study the importance of microphysical feedback processes in response to anthropogenic aerosols in orographic mixed-phase clouds. Our methods can be extended to other cloud regimes as well as dynamical and thermodynamical feedbacks. For our simulations, we use the regional atmospheric model COSMO-ART-M7 in a 2D setup with an idealized mountain. To capture major processes from aerosol emission to precipitation, the model is coupled to a modal aerosol scheme and includes aerosol activation and heterogeneous freezing as well as two-moment cold and warm cloud microphysics. We perform simulations with aerosol conditions that vary in amount and chemical composition and thus perturb the warm- and ice-phase pathways of precipitation formation and their mixed-phase interactions. Our analysis is based on quantifying the interaction strength between aerosol, cloud and precipitation variables by susceptibilities, i.e. relative sensitivities d ln(Y) / d ln(X), where the change in variable Y is a response to a perturbation in variable X. We describe how to decompose susceptibilities into a direct response expected from the parameterization and a contribution from feedbacks. Resilience features similar magnitudes but opposite signs for those contributions, resulting in an overall small susceptibility. We find considerable contributions from feedbacks, which appear more important for warm-phase than for cold-phase processes. We do not observe, however, a trend for resilience in mixed-phase cloud microphysics. Moreover, feedback contributions seem of secondary importance when compared to the strong dependence of susceptibilities on the microphysical state of the cloud.

  6. Deriving aerosol hygroscopic mixing state from size-resolved CCN activity and HR-ToF-AMS measurements

    NASA Astrophysics Data System (ADS)

    Bhattu, Deepika; Tripathi, S. N.; Chakraborty, Abhishek

    2016-10-01

    The ability of a particle to uptake water and form a cloud droplet depends on its hygroscopicity. To understand its impact on cloud properties and ultimately radiative forcing, knowledge of chemically-resolved mixing state information or the one based on hygroscopic growth is crucial. Typically, global models assume either pure internal or external mixing state which might not be true for all conditions and sampling locations. To investigate into this, the current study employed an indirect approach to infer the probable mixing state. The hygroscopic parameters derived from κ-Kohler theory using size-resolved CCN measurements (κCCN) and bulk/size-resolved aerosol mass spectrometer (AMS) measurements (κAMS) were compared. The accumulation mode particles were found to be more hygroscopic (κCCN = 0.24) than Aitken mode (κCCN = 0.13), perhaps due to increased ratio of inorganic to organic mass fraction. The activation diameter calculated from size-resolved CCN activity measurements at 5 different supersaturation (SS) levels varied in the range of 115 nm-42 nm with κCCN = 0.13-0.23 (avg = 0.18 ± 0.10 (±1σ)). Further, κAMS>κCCN was observed possibly due to the fact that organic and inorganic mass present in the Aitken mode was not correctly represented by bulk chemical composition and size-resolved fractional contribution of oxidized OA was not accurately accounted. Better correlation of organic fraction (forg) and κCCN at lower SS explained this behaviour. The decrease in κCCN with the time of the day was more pronounced at lower SS because of the relative mass reduction of soluble inorganic species by ∼17%. Despite the large differences between κ measured from two approaches, less over-prediction (up to 18%) between measured and predicted CCN concentration suggested lower impact of chemical composition and mixing state at higher SS. However, at lower SS, presences of externally mixed CCN-inactive aerosols lead to CCN over-prediction reflecting the

  7. Differences in the OC/EC Ratios that Characterize Ambient and Source Aerosols due to Thermal-Optical Analysis

    EPA Science Inventory

    Thermal-optical analysis (TOA) is typically used to measure the OC/EC (organic carbon/elemental carbon) and EC/TC (elemental carbon/total carbon) ratios in source and atmospheric aerosols. The present study utilizes a dual-optical carbon aerosol analyzer to examine the effects of...

  8. Simulating the Evolution of Soot Mixing State with a Particle-Resolved Aerosol Model

    SciTech Connect

    Riemer, Nicole; West, Matt; Zaveri, Rahul A.; Easter, Richard C.

    2009-05-05

    The mixing state of soot particles in the atmosphere is of crucial importance for assessing their climatic impact, since it governs their chemical reactivity, cloud condensation nuclei activity and radiative properties. To improve the mixing state representation in models, we present a new approach, the stochastic particle-resolved model PartMC-MOSAIC, which explicitly resolves the composition of individual particles in a given population of different types of aerosol particles. This approach accurately tracks the evolution of the mixing state of particles due to emission, dilution, condensation and coagulation. To make this direct stochastic particle-based method practical, we implemented a new multiscale stochastic coagulation method. With this method we achieved optimal efficiency for applications when the coagulation kernel is highly non-uniform, as is the case for many realistic applications. PartMC-MOSAIC was applied to an idealized urban plume case representative of a large urban area to simulate the evolution of carbonaceous aerosols of different types due to coagulation and condensation. For this urban plume scenario we quantified the individual processes that contribute to the aging of the aerosol distribution, illustrating the capabilities of our modeling approach. The results showed for the first time the multidimensional structure of particle composition, which is usually lost in internally-mixed sectional or modal aerosol models.

  9. Fine Iron Aerosols Are Internally Mixed with Nitrate in the Urban European Atmosphere.

    PubMed

    Dall'Osto, Manuel; Beddows, D C S; Harrison, Roy M; Onat, Burcu

    2016-04-19

    Atmospheric iron aerosol is a bioavailable essential nutrient playing a role in oceanic productivity. Using aerosol time-of-flight mass spectrometry (ATOFMS), the particle size (0.3-1.5 μm), chemical composition and mixing state of Fe-containing particles collected at two European urban sites (London and Barcelona) were characterized. Out of the six particle types accounting for the entire Fe-aerosol population, that arising from long-range transport (LRT) of fine Fe-containing particles (Fe-LRT, 54-82% across the two sites) was predominant. This particle type was found to be internally mixed with nitrate and not with sulfate, and likely mostly associated with urban traffic activities. This is in profound contrast with previous studies carried out in Asia, where the majority of iron-containing particles are mixed with sulfate and are of coal combustion origin. Other minor fine iron aerosol sources included mineral dust (8-11%), traffic brake wear material (1-17%), shipping/oil (1-6%), biomass combustion (4-13%) and vegetative debris (1-3%). Overall, relative to anthropogenic Asian Fe-sulfate dust, anthropogenic European dust internally mixed with additional key nutrients such as nitrate is likely to play a different role in ocean global biogeochemical cycles.

  10. Chemical imaging of ambient aerosol particles: Observational constraints on mixing state parameterization

    DOE PAGES

    O'Brien, Rachel E.; Wang, Bingbing; Laskin, Alexander; ...

    2015-08-26

    In this study, a new parameterization for quantifying the mixing state of aerosol populations has been applied for the first time to samples of ambient particles analyzed using spectro-microscopy techniques. Scanning transmission X-ray microscopy/near edge X-ray absorption fine structure (STXM/NEXAFS) and computer-controlled scanning electron microscopy/energy dispersive X-ray spectroscopy (CCSEM/EDX) were used to probe the composition of the organic and inorganic fraction of individual particles collected on 27 and 28 June during the 2010 Carbonaceous Aerosols and Radiative Effects study in the Central Valley, California. The first field site, T0, was located in downtown Sacramento, while T1 was located near themore » Sierra Nevada Mountains. Mass estimates of the aerosol particle components were used to calculate mixing state metrics, such as the particle-specific diversity, bulk population diversity, and mixing state index, for each sample. The STXM data showed evidence of changes in the mixing state associated with a buildup of organic matter confirmed by collocated measurements, and the largest impact on the mixing state was due to an increase in soot dominant particles during this buildup. The mixing state from STXM was similar between T0 and T1, indicating that the increased organic fraction at T1 had a small effect on the mixing state of the population. The CCSEM/EDX analysis showed the presence of two types of particle populations: the first was dominated by aged sea-salt particles and had a higher mixing state index (indicating a more homogeneous population); the second was dominated by carbonaceous particles and had a lower mixing state index.« less

  11. Chemical imaging of ambient aerosol particles: Observational constraints on mixing state parameterization

    SciTech Connect

    O'Brien, Rachel E.; Wang, Bingbing; Laskin, Alexander; Riemer, Nicole; West, Matthew; Zhang, Qi; Sun, Yele; Yu, Xiao -Ying; Alpert, Peter; Knopf, Daniel A.; Gilles, Mary K.; Moffet, Ryan C.

    2015-08-26

    In this study, a new parameterization for quantifying the mixing state of aerosol populations has been applied for the first time to samples of ambient particles analyzed using spectro-microscopy techniques. Scanning transmission X-ray microscopy/near edge X-ray absorption fine structure (STXM/NEXAFS) and computer-controlled scanning electron microscopy/energy dispersive X-ray spectroscopy (CCSEM/EDX) were used to probe the composition of the organic and inorganic fraction of individual particles collected on 27 and 28 June during the 2010 Carbonaceous Aerosols and Radiative Effects study in the Central Valley, California. The first field site, T0, was located in downtown Sacramento, while T1 was located near the Sierra Nevada Mountains. Mass estimates of the aerosol particle components were used to calculate mixing state metrics, such as the particle-specific diversity, bulk population diversity, and mixing state index, for each sample. The STXM data showed evidence of changes in the mixing state associated with a buildup of organic matter confirmed by collocated measurements, and the largest impact on the mixing state was due to an increase in soot dominant particles during this buildup. The mixing state from STXM was similar between T0 and T1, indicating that the increased organic fraction at T1 had a small effect on the mixing state of the population. The CCSEM/EDX analysis showed the presence of two types of particle populations: the first was dominated by aged sea-salt particles and had a higher mixing state index (indicating a more homogeneous population); the second was dominated by carbonaceous particles and had a lower mixing state index.

  12. Numerical investigation of the coagulation mixing between dust and hygroscopic aerosol particles and its impacts

    NASA Astrophysics Data System (ADS)

    Tsai, I.-Chun; Chen, Jen-Ping; Lin, Yi-Chiu; Chung-Kuang Chou, Charles; Chen, Wei-Nai

    2015-05-01

    A statistical-numerical aerosol parameterization was incorporated into the Community Multiscale Air Quality modeling system to study the coagulation mixing process focusing on a dust storm event that occurred over East Asia. Simulation results show that the coagulation mixing process tends to decrease aerosol mass, surface area, and number concentrations over the dust source areas. Over the downwind oceanic areas, aerosol concentrations generally increased due to enhanced sedimentation as particles became larger upon coagulation. The mixture process can reduce the overall single-scattering albedo by up to 10% as a result of enhanced core with shell absorption by dust and reduction in the number of scattering particles. The enhanced dry deposition speed also altered the vertical distribution. In addition, the ability of aerosol particles to serve as cloud condensation nuclei (CCN) increased from around 107 m-3 to above 109 m-3 over downwind areas because a large amount of mineral dust particles became effective CCN with solute coating, except over the highly polluted areas where multiple collections of hygroscopic particles by dust in effect reduced CCN number. This CCN effect is much stronger for coagulation mixing than by the uptake of sulfuric acid gas on dust, although the nitric acid gas uptake was not investigated. The ability of dust particles to serve as ice nuclei may decrease or increase at low or high subzero temperatures, respectively, due to the switching from deposition nucleation to immersion freezing or haze freezing.

  13. Mixed-layer ocean responses to anthropogenic aerosol dimming from 1870 to 2000

    NASA Astrophysics Data System (ADS)

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

    2016-04-01

    It is still debated, to what extent anthropogenic aerosol-induced changes in surface solar radiation (SSR) since industrialization affected surface temperatures (tsurf). We use mixed-layer ocean (MLO) experiments with the general circulation model ECHAM6.1 and explicit aerosols (HAM2.2) to identify regions where this effect is discernible. For each decade from 1870 to 2000 we derive three equilibria: anthropogenic aerosol emissions and greenhouse gas concentrations at the respective decade's levels (ALL), either aerosols or greenhouse gases fixed at year 1850 levels (GHG and AERO). We duplicated parts of the experiments with different prescribed divergence of ocean heat transport (Q_ALL, Q_AERO, Q_GHG). Comparing year 2000 with year 1870 equilibria, we find global average cooling of -1.4K for AERO, and warming of 1.4K for GHG. ALL and Q_ALL warm by 0.6K and 0.4K, respectively. The way divergence of ocean heat transport is prescribed thus matters. Pattern correlations of year 2000 tsurf responses in ALL with the sum of AERO and GHG are higher (0.88) than with Q_ALL (0.71) confirming additivity of global patterns, but not of global means. The imprint of anthropogenic aerosols on tsurf response patterns in ALL is distinct, thus potentially detectable. Over the decades, ocean fractions affected by either changing aerosol optical depth or all-sky SSR vary in concert, supporting linkage between anthropogenic aerosols and all-sky SSR. SSR changes and tsurf responses are marginally collocated. Oceanic regions with strongest tsurf response to aerosol-induced SSR changes are the northern mid-latitudes and North Pacific with tsurf sensitivities up to -0.7K per Wm-2 SSR change. Results presented have been published under the same title in the Journal of Geophysical Research, Volume 121, DOI 10.1002/2015JD024070.

  14. Mixed-layer ocean responses to anthropogenic aerosol dimming from 1870 to 2000

    NASA Astrophysics Data System (ADS)

    Dallafior, T. N.; Folini, D.; Knutti, R.; Wild, M.

    2016-01-01

    It is debated to what extent surface solar radiation (SSR) changes through varying anthropogenic aerosol emissions since industrialization affected surface temperatures (tsurf). We use mixed-layer ocean experiments with the general circulation model ECHAM6.1 and explicit aerosols (HAM2.2) to identify regions where this effect is discernible. For each decade from 1870 to 2000 we derive three equilibria: anthropogenic aerosol emissions and greenhouse gas concentrations at the respective decade's levels (ALL), either aerosols or greenhouse gases fixed at year 1850 levels (GHG and AERO). We duplicated parts of the experiments with different prescribed divergence of ocean heat transport (Q_ALL, Q_AERO, and Q_GHG). Comparing year 2000 with year 1870 equilibria, we find global average cooling of -1.4 K for AERO and warming of 1.4 K for GHG. ALL and Q_ALL warm by 0.6 K and 0.4 K, respectively. The way divergence of ocean heat transport is prescribed thus matters. Pattern correlations of year 2000 tsurf responses in ALL with the sum of AERO and GHG are higher (0.88) than with Q_ALL (0.71) confirming additivity of global patterns, but not of global means. The imprint of anthropogenic aerosols on tsurf response patterns in ALL is distinct, thus potentially detectable. Over the decades, ocean fractions affected by either changing aerosol optical depth or all-sky SSR vary in concert, supporting linkage between anthropogenic aerosols and all-sky SSR. SSR changes and tsurf responses are marginally collocated. Oceanic regions with strongest tsurf response to aerosol-induced SSR changes are the northern midlatitudes and North Pacific with tsurf sensitivities up to -0.7 K W m-2 SSR change.

  15. Particle-Resolved Modeling of Aerosol Mixing State in an Evolving Ship Plume

    NASA Astrophysics Data System (ADS)

    Riemer, N. S.; Tian, J.; Pfaffenberger, L.; Schlager, H.; Petzold, A.

    2011-12-01

    The aerosol mixing state is important since it impacts the particles' optical and CCN properties and thereby their climate impact. It evolves continuously during the particles' residence time in the atmosphere as a result of coagulation with other particles and condensation of secondary aerosol species. This evolution is challenging to represent in traditional aerosol models since they require the representation of a multi-dimensional particle distribution. While modal or sectional aerosol representations cannot practically resolve the aerosol mixing state for more than a few species, particle-resolved models store the composition of many individual aerosol particles directly. They thus sample the high-dimensional composition state space very efficiently and so can deal with tens of species, fully resolving the mixing state. Here we use the capabilities of the particle-resolved model PartMC-MOSAIC to simulate the evolution of particulate matter emitted from marine diesel engines and compare the results to aircraft measurements made in the English Channel in 2007 as part of the European campaign QUANTIFY. The model was initialized with values of gas concentrations and particle size distributions and compositions representing fresh ship emissions. These values were obtained from a test rig study in the European project HERCULES in 2006 using a serial four-stroke marine diesel engine operating on high-sulfur heavy fuel oil. The freshly emitted particles consisted of sulfate, black carbon, organic carbon and ash. We then tracked the particle population for several hours as it evolved undergoing coagulation, dilution with the background air, and chemical transformations in the aerosol and gas phase. This simulation was used to compute the evolution of CCN properties and optical properties of the plume on a per-particle basis. We compared our results to size-resolved data of aged ship plumes from the QUANTIFY Study in 2007 and showed that the model was able to reproduce

  16. Chemical Imaging of Ambient Aerosol Particles: Observational Constraints on Mixing State Parameterization

    SciTech Connect

    O'Brien, Rachel; Wang, Bingbing; Laskin, Alexander; Riemer, Nicole; West, Matthew; Zhang, Qi; Sun, Yele; Yu, Xiao-Ying; Alpert, Peter A.; Knopf, Daniel A.; Gilles, Mary K.; Moffet, Ryan

    2015-09-28

    A new parameterization for quantifying the mixing state of aerosol populations has been applied for the first time to samples of ambient particles analyzed using spectro-microscopy techniques. Scanning transmission x-ray microscopy/near edge x-ray absorption fine structure (STXM/NEXAFS) and computer controlled scanning electron microscopy/energy dispersive x-ray spectroscopy (CCSEM/EDX) were used to probe the composition of the organic and inorganic fraction of individual particles collected on June 27th and 28th during the 2010 Carbonaceous Aerosols and Radiative Effects (CARES) study in the Central Valley, California. The first field site, T0, was located in downtown Sacramento, while T1 was located near the Sierra Nevada Mountains. Mass estimates of the aerosol particle components were used to calculate mixing state metrics, such as the particle-specific diversity, bulk population diversity, and mixing state index, for each sample. Both microscopy imaging techniques showed more changes over these two days in the mixing state at the T0 site than at the T1 site. The STXM data showed evidence of changes in the mixing state associated with a build-up of organic matter confirmed by collocated measurements and the largest impact on the mixing state was due to an increase in soot dominant particles during this build-up. The CCSEM/EDX analysis showed the presence of two types of particle populations; the first was dominated by aged sea salt particles and had a higher mixing state index (indicating a more homogeneous population), the second was dominated by carbonaceous particles and had a lower mixing state index.

  17. Retrieval of Aerosol Optical Depth in Vicinity of Broken Clouds from Reflectance Ratios: Case Study

    SciTech Connect

    Kassianov, Evgueni I.; Ovchinnikov, Mikhail; Berg, Larry K.; McFarlane, Sally A.; Flynn, Connor J.; Ferrare, Richard; Hostetler, Chris A.; Alexandrov, Mikhail

    2010-10-06

    A recently developed reflectance ratio (RR) method for the retrieval of aerosol optical depth (AOD) is evaluated using extensive airborne and ground-based data sets collected during the Cloud and Land Surface Interaction Campaign (CLASIC) and the Cumulus Humilis Aerosol Processing Study (CHAPS), which took place in June 2007 over the U.S. Department of Energy (DOE) Atmospheric Radiation Measurement (ARM) Southern Great Plains site. A detailed case study is performed for a field of single-layer shallow cumuli observed on June 12, 2007. The RR method is applied to retrieve the spectral values of AOD from the reflectance ratios measured by the MODIS Airborne Simulator (MAS) for two pairs of wavelengths (660 and 470 nm and 870 and 470 nm) collected at a spatial resolution of 0.05 km. The retrieval is compared with an independent AOD estimate from three ground-based Multi-filter Rotating Shadowband Radiometers (MFRSRs). The interpolation algorithm that is used to project MFRSR point measurements onto the aircraft flight tracks is tested using AOD derived from NASA Langley High Spectral Resolution Lidar (HSRL). The RR AOD estimates are in a good agreement (within 5%) with the MFRSR-derived AOD values for the 660-nm wavelength. The AODs obtained from MAS reflectance ratios overestimate those derived from MFRSR measurements by 15-30% for the 470-nm wavelength and underestimate the 870-nm AOD by the same amount.

  18. Impact of mixing state and hygroscopicity on CCN activity of biomass burning aerosol in Amazonia

    NASA Astrophysics Data System (ADS)

    Sánchez Gácita, Madeleine; Longo, Karla M.; Freire, Julliana L. M.; Freitas, Saulo R.; Martin, Scot T.

    2017-02-01

    Smoke aerosols prevail throughout Amazonia because of widespread biomass burning during the dry season, and external mixing, low variability in the particle size distribution and low particle hygroscopicity are typical. There can be profound effects on cloud properties. This study uses an adiabatic cloud model to simulate the activation of smoke particles as cloud condensation nuclei (CCN) for three hypothetical case studies, chosen as to resemble biomass burning aerosol observations in Amazonia. The relative importance of variability in hygroscopicity, mixing state, and activation kinetics for the activated fraction and maximum supersaturation is assessed. For a population with κp = 0.04, an overestimation of the cloud droplet number concentration Nd for the three selected case studies between 22.4 ± 1.4 and 54.3 ± 3.7 % was obtained when assuming a hygroscopicity parameter κp = 0.20. Assuming internal mixing of the aerosol population led to overestimations of up to 20 % of Nd when a group of particles with medium hygroscopicity was present in the externally mixed population cases. However, the overestimations were below 10 % for external mixtures between very low and low-hygroscopicity particles, as seems to be the case for Amazon smoke particles. Kinetic limitations were significant for medium- and high-hygroscopicity particles, and much lower for very low and low-hygroscopicity particles. When particles were assumed to be at equilibrium and to respond instantly to changes in the air parcel supersaturation, the overestimation of the droplet concentration was up to ˜ 100 % in internally mixed populations, and up to ˜ 250 % in externally mixed ones, being larger for the higher values of hygroscopicity. In addition, a perceptible delay between the times when maximum supersaturation and maximum aerosol activated fraction are reached was noticed and, for aerosol populations with effective hygroscopicity κpeff higher than a certain threshold value, the delay in

  19. Optical Properties of Internally Mixed Aerosol Particles Composed of Dicarboxylic Acids and Ammonium Sulfate

    NASA Astrophysics Data System (ADS)

    Freedman, Miriam A.; Hasenkopf, Christa A.; Beaver, Melinda R.; Tolbert, Margaret A.

    2009-10-01

    We have investigated the optical properties of internally mixed aerosol particles composed of dicarboxylic acids and ammonium sulfate using cavity ring-down aerosol extinction spectroscopy at a wavelength of 532 nm. The real refractive indices of these nonabsorbing species were retrieved from the extinction and concentration of the particles using Mie scattering theory. We obtain refractive indices for pure ammonium sulfate and pure dicarboxylic acids that are consistent with literature values, where they exist, to within experimental error. For mixed particles, however, our data deviates significantly from a volume-weighted average of the pure components. Surprisingly, the real refractive indices of internal mixtures of succinic acid and ammonium sulfate are higher than either of the pure components at the highest organic weight fractions. For binary internal mixtures of oxalic or adipic acid with ammonium sulfate, the real refractive indices of the mixtures are approximately the same as ammonium sulfate for all organic weight fractions. Various optical mixing rules for homogeneous and slightly heterogeneous systems fail to explain the experimental real refractive indices. It is likely that complex particle morphologies are responsible for the observed behavior of the mixed particles. Implications of our results for atmospheric modeling and aerosol structure are discussed.

  20. Modeling the Thermodynamics of Mixed Organic-Inorganic Aerosols to Predict Water Activities and Phase Equilibria

    NASA Astrophysics Data System (ADS)

    Zuend, A.; Marcolli, C.; Luo, B.; Peter, T.

    2008-12-01

    Tropospheric aerosol particles contain mixtures of inorganic salts, acids, water, and a large variety of organic compounds. Interactions between these substances in liquid mixtures lead to discrepancies from ideal thermodynamic behavior. While the thermodynamics of aqueous inorganic systems at atmospheric temperatures are well established, little is known about the physicochemistry of mixed organic-inorganic particles. Salting-out and salting-in effects result from organic-inorganic interactions and are used to improve industrial separation processes. In the atmosphere, they may influence the aerosol phases. Liquid-liquid phase separations into a mainly polar (aqueous) and a less polar organic phase may considerably influence the gas/particle partitioning of semi-volatile substances compared to a single phase estimation. Moreover, the phases present in the aerosol define the reaction medium for heterogeneous and multiphase chemistry occurring in aerosol particles. A correct description of these phases is needed when gas- or cloud-phase reaction schemes are adapted to aerosols. Non-ideal thermodynamic behavior in mixtures is usually described by an expression for the excess Gibbs energy. We present the group-contribution model AIOMFAC (Aerosol Inorganic-Organic Mixtures Functional groups Activity Coefficients), which explicitly accounts for molecular interactions between solution constituents, both organic and inorganic, to calculate activities, chemical potentials and the total Gibbs energy of mixed systems. This model allows to compute vapor-liquid (VLE), liquid-liquid (LLE) and solid-liquid (SLE) equilibria within one framework. Focusing on atmospheric applications we considered eight different cations, five anions and a wide range of alcohols/polyols as organic compounds. With AIOMFAC, the activities of the components within an aqueous electrolyte solution are very well represented up to high ionic strength. We show that the semiempirical middle

  1. Black carbon aerosol optical properties are influenced by initial mixing state

    NASA Astrophysics Data System (ADS)

    Willis, M. D.; Healy, R. M.; Riemer, N.; West, M.; Wang, J. M.; Jeong, C. H.; Wenger, J.; Abbatt, J.; Lee, A.

    2015-12-01

    Incomplete combustion emits teragram quantities of black carbon (BC) aerosol to the troposphere each year, resulting in a significant warming effect on climate that may be second only to carbon dioxide. The magnitude of BC impacts on a global scale remains poorly constrained and is intimately related to its particle-scale physical and chemical properties. Using particle-resolved modeling informed by novel quantitative measurements from an Aerodyne soot-particle aerosol mass spectrometer (SP-AMS), we show that initial mixing state (or the distribution of co-emitted components amongst fresh BC-containing particles) significantly affects BC-aerosol optical properties even after a day of atmospheric processing. Both single particle and ensemble observations indicate that BC near emission co-exists with hydrocarbon-like organic aerosol (HOA) in two distinct particle types: HOA-rich and BC-rich particles. The average mass fraction of black carbon (mfBC) in HOA- and BC-rich particle types was 0.02-0.08 and 0.72-0.93, respectively. Notably, positive matrix factorization (PMF) analysis of ensemble SP-AMS measurements indicates that BC-rich particles contribute the majority of BC mass (> 90%) in freshly emitted particles. This new measurement capability provides quantitative insight into the physical and chemical nature of BC-containing particles and is used to drive a particle-resolved aerosol box model. Significant differences in calculated single scattering albedo (an increase of 0.1) arise from accurate treatment of initial particle mixing state as compared to the assumption of uniform aerosol composition at the point of BC injection to the atmosphere.

  2. 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

    The use of co-located multiple spectroscopic techniques can provide detailed information on the atmospheric processes regulating aerosol chemical composition and mixing state. So far, field campaigns heavily equipped with aerosol mass spectrometers have been carried out mainly in large conurbations and in areas directly affected by their outflow, whereas lesser efforts have been dedicated to continental areas characterised by a less dense urbanisation. We present here the results obtained at a background site in the Po Valley, Italy, in summer 2009. For the first time in Europe, six state-of-the-art spectrometric techniques were used in parallel: aerosol time-of-flight mass spectrometer (ATOFMS), two aerosol mass spectrometers (high-resolution time-of-flight aerosol mass spectrometer - HR-ToF-AMS and soot particle aerosol mass spectrometer - SP-AMS), thermal desorption aerosol gas chromatography (TAG), chemical ionisation mass spectrometry (CIMS) and (offline) proton nuclear magnetic resonance (1H-NMR) spectroscopy. The results indicate that, under high-pressure conditions, atmospheric stratification at night and early morning hours led to the accumulation of aerosols produced by anthropogenic sources distributed over the Po Valley plain. Such aerosols include primary components such as black carbon (BC), secondary semivolatile compounds such as ammonium nitrate and amines and a class of monocarboxylic acids which correspond to the AMS cooking organic aerosol (COA) already identified in urban areas. In daytime, the entrainment of aged air masses in the mixing layer is responsible for the accumulation of low-volatility oxygenated organic aerosol (LV-OOA) and also for the recycling of non-volatile primary species such as black carbon. According to organic aerosol source apportionment, anthropogenic aerosols accumulating in the lower layers overnight accounted for 38% of organic aerosol mass on average, another 21% was accounted for by aerosols recirculated in

  3. Modeling immersion freezing with aerosol-dependent prognostic ice nuclei in Arctic mixed-phase clouds

    NASA Astrophysics Data System (ADS)

    Paukert, M.; Hoose, C.

    2014-07-01

    While recent laboratory experiments have thoroughly quantified the ice nucleation efficiency of different aerosol species, the resulting ice nucleation parameterizations have not yet been extensively evaluated in models on different scales. Here the implementation of an immersion freezing parameterization based on laboratory measurements of the ice nucleation active surface site density of mineral dust and ice nucleation active bacteria, accounting for nucleation scavenging of ice nuclei, into a cloud-resolving model with two-moment cloud microphysics is presented. We simulated an Arctic mixed-phase stratocumulus cloud observed during Flight 31 of the Indirect and Semi-Direct Aerosol Campaign near Barrow, Alaska. Through different feedback cycles, the persistence of the cloud strongly depends on the ice number concentration. It is attempted to bring the observed cloud properties, assumptions on aerosol concentration, and composition and ice formation parameterized as a function of these aerosol properties into agreement. Depending on the aerosol concentration and on the ice crystal properties, the simulated clouds are classified as growing, dissipating, and quasi-stable. In comparison to the default ice nucleation scheme, the new scheme requires higher aerosol concentrations to maintain a quasi-stable cloud. The simulations suggest that in the temperature range of this specific case, mineral dust can only contribute to a minor part of the ice formation. The importance of ice nucleation active bacteria and possibly other ice formation modes than immersion freezing remains poorly constrained in the considered case, since knowledge on local variations in the emissions of ice nucleation active organic aerosols in the Arctic is scarce.

  4. Mixing state and spectral absorption of atmospheric aerosols observed at a marine background site

    NASA Astrophysics Data System (ADS)

    Cayetano, M. G.; Lee, K. Y.; Kim, Y. J.

    2011-12-01

    Mineral dust and sea salt particles are portions of atmospheric aerosols in Korea due to the periodic transport of loess dust particles from Gobi and Taklimakan deserts in west China, as well as the sea salt enrichment of atmospheric particles from the seas surrounding the Korean peninsula [Kim et al., 2009; Sahu et al., 2009]. Carbonaceous particles and secondary inorganic aerosols (sulphates and nitrates) are ubiquitous due to the proliferating biomass burning [Ryu et al., 2004], as well as the increasing use of fossil fuels locally and by regional transport from neighbouring countries. Collectively, when these aerosols are transported, their compositions are further modified due to the aging process, impacting their physico-chemical properties including spectral absorption. In order to investigate the spectral response of the absorption under different ambient aerosol conditions, measurements have been conducted at a marine background site in Korea (Deokjeok Island. 37° 13' 33" N, 126° 8' 51" E) during the spring (13 days) and fall (8 days) seasons of 2009 using an aethalometer (Magee AE31), a nephelometer (Optec NGN2a) and other supporting instruments (PILS-IC, PM2.5 cyclone samplers for off-line OC/EC measurements). It has been found that spring aerosols were dominated by sulphate-rich and carbonaceous-rich fractions (21.4%±8.0% and 28.8%±7.9%, respectively), with an Angström exponent of absorption, αabs = 1.3±0.1 at 370-950 nm. The fall season aerosols were grouped based on their chemical composition as acidic aerosols, dust-enriched, and seasalt-enriched aerosols. Angström exponent of absorption, αabs for acidic aerosols was obtained to be 1.3±0.2 at 370-950 nm. However, dust enriched aerosols showed increased absorption in the short UV-Vis range (370-590 nm), which can be attributed to their mixing with light absorbing aerosols. Different types of aerosols exhibit different spectral absorption characteristics depending on their composition and

  5. Extinction-to-Backscatter Ratios of Lofted Aerosol Layers Observed During the First Three Months of CALIPSO Measurements

    NASA Technical Reports Server (NTRS)

    Omar, Ali H.; Vaughan, Mark A.; Liu, Zhaoyan; Hu, Yongxiang; Reagan, John A.; Winker, David M.

    2007-01-01

    Case studies from the first three months of the Cloud and Aerosol Lidar and Infrared Pathfinder Spaceborne Observations (CALIPSO) measurements of lofted aerosol layers are analyzed using transmittance [Young, 1995] and two-wavelength algorithms [Vaughan et al., 2004] to determine the aerosol extinction-to-backscatter ratios at 532 and 1064 nm. The transmittance method requires clear air below the layer so that the transmittance through the layer can be determined. Suitable scenes are selected from the browse images and clear air below features is identified by low 532 nm backscatter signal and confirmed by low depolarization and color ratios. The transmittance and two-wavelength techniques are applied to a number of lofted layers and the extinction-to-backscatter ratios are compared with values obtained from the CALIPSO aerosol models [Omar et al., 2004]. The results obtained from these studies are used to adjust the aerosol models and develop observations based extinction-to-backscatter ratio look-up tables and phase functions. Values obtained by these techniques are compared to Sa determinations using other independent methods with a goal of developing probability distribution functions of aerosol type-specific extinction to backscatter ratios. In particular, the results are compared to values determined directly by the High Spectral Resolution Lidar (HSRL) during the CALIPSO CloudSat Validation Experiments (CCVEX) and Sa determined by the application of the two-wavelength lidar Constrained Ratio Aerosol Model-fit (CRAM) retrieval approach [Cattrall et al., 2005; Reagan et al., 2004] to the HSRL data. The results are also compared to values derived using the empirical relationship between the multiple-scattering fraction and the linear depolarization ratio by using Monte Carlo simulations of water clouds [Hu et al., 2006].

  6. On deriving the accurate aerosol extinction profiles in the troposphere and lower stratosphere using the range dependent scattering ratio

    NASA Astrophysics Data System (ADS)

    Satyanarayana, M. V.; Radhakrishnan, S. R.; Mahadevanpillai, V. P.; Krishnakumar, V.

    2008-12-01

    Lidar has proven to be an effective instrument for obtaining high resolution profiles of atmospheric aerosols. Deriving the optical properties of aerosols from the experimentally obtained lidar data is one of the most interesting and challenging task for the atmospheric scientists. A few methods had been developed so far, to obtain the quantitative profiles of extinction and backscattering coefficient of aerosols from the pulsed backscattering lidar measurements. Most of the existing inversion methods assume a range independent value for the scattering ratio for inverting the lidar signal even though it is known that the scattering ratio depends on the nature of aerosols and as such range dependent. We used a modified Klett's method for the inversion of lidar signal that uses range dependent scattering ratio (s) for the characterization of atmospheric aerosols. This method provides the constants k and s for all the altitude regions of the atmosphere and leads to derive the aerosol extinction profile for the lidar data. In this paper we made a study on the errors involved in the extinction profiles derived using the range dependent scattering ratio and discuss the approach in this regard to obtain the accurate extinction profiles.

  7. Retrieval of water vapor mixing ratio from a multiple channel Raman-scatter lidar using an optimal estimation method.

    PubMed

    Sica, R J; Haefele, A

    2016-02-01

    Lidar measurements of the atmospheric water vapor mixing ratio provide an excellent complement to radiosoundings and passive, ground-based remote sensors. Lidars are now routinely used that can make high spatial-temporal resolution measurements of water vapor from the surface to the stratosphere. Many of these systems can operate during the day and night, with operation only limited by clouds thick enough to significantly attenuate the laser beam. To enhance the value of these measurements for weather and climate studies, this paper presents an optimal estimation method (OEM) to retrieve the water vapor mixing ratio, aerosol optical depth profile, Ångstrom exponent, lidar constants, detector dead times, and measurement backgrounds from multichannel vibrational Raman-scatter lidars. The OEM retrieval provides the systematic uncertainties due to the overlap function, calibration factor, air density and Rayleigh-scatter cross sections, in addition to the random uncertainties of the retrieval due to measurement noise. The OEM also gives the vertical resolution of the retrieval as a function of height, as well as the height to which the contribution of the a priori is small. The OEM is applied to measurements made by the Meteoswiss Raman Lidar for Meteorological Observations (RALMO) in the day and night for clear and cloudy conditions. The retrieved water vapor mixing ratio is in excellent agreement with both the traditional lidar retrieval method and coincident radiosoundings.

  8. Retrieval of Aerosol Optical Depth in Vicinity of Broken Clouds from Reflectance Ratios: A Novel Approach

    SciTech Connect

    Kassianov, Evgueni I.; Ovtchinnikov, Mikhail; Berg, Larry K.; McFarlane, Sally A.; Flynn, Connor J.

    2008-10-13

    A novel method for the retrieval of aerosol optical depth (AOD) under partly cloudy conditions has been suggested. The method exploits reflectance ratios, which are not sensitive to the three-dimensional (3D) effects of clouds. As a result, the new method provides an effective way to avoid the 3D cloud effects, which otherwise would have a large (up to 140%) contaminating impact on the aerosol retrievals. The 1D version of the radiative transfer model has been used to develop look-up tables (LUTs) of reflectance ratios as functions of two parameters describing the spectral dependence of AOD (a power law). The new method implements an innovative 2D inversion for simultaneous retrieval of these two parameters and, thus, the spectral behavior of AOD. The performance of the new method has been illustrated with a model-output inverse problem. We demonstrated that a new retrieval has the potential for (i) detection of clear pixels outside of cloud shadows and (ii) accurate (~15%) estimation of AOD for the majority of them.

  9. The effect of water to ethanol feed ratio on physical properties and aerosolization behavior of spray dried cromolyn sodium particles.

    PubMed

    Gilani, Kambiz; Najafabadi, Abdolhossien Rouholamini; Barghi, Mohammadali; Rafiee-Tehrani, Morteza

    2005-05-01

    Cromolyn sodium (CS) was spray dried under constant operation conditions from different water to ethanol feed ratios (50:50-0:100). The spray dried CS samples were characterized for their physicochemical properties including crystallinity, particle size distribution, morphology, density, and water/ethanol content. To determine quantitatively the crystallinity of the powders, an X-ray diffraction (XRD) method was developed using samples with different crystallinity prepared by physical mixing of 100% amorphous and 100% crystalline CS materials. The aerodynamic behavior of the CS samples was determined using an Andersen Cascade Impactor (ACI) with a Spinhaler at an air flow of 60 L/min. Binary mixtures of each spray dried CS powder and Pharmatose 325, a commercial alpha-lactose monohydrate available for DPI formulations, were prepared and in vitro aerosol deposition of the drug from the mixtures was analyzed using ACI to evaluate the effect of carrier on deposition profiles of the spray dried samples. CS spray dried from absolute ethanol exhibited XRD pattern characteristic for crystalline materials and different from patterns of the other samples. The crystallinity of spray dried CS obtained in the presence of water varied from 0% to 28.37%, depending on the ratio of water to ethanol in the feed suspensions. All samples presented different particle size, water/ethanol content, and bulk density values. CS particles spray dried from absolute ethanol presented uniform elongated shape whereas the other samples consisted mainly of particles with irregular shape. Overall, fine particle fraction increased significantly (p < 0.01) with decreasing d50% and water and ethanol content of spray dried CS samples. Significant difference (p < 0.01) in deposition profiles of the drug were observed between corresponding carrier free and carrier blended formulations. The difference in deposition profiles of CS aerosolized from various spray dried samples were described according to

  10. Determination of the organic aerosol mass to organic carbon ratio in IMPROVE samples.

    PubMed

    El-Zanan, Hazem S; Lowenthal, Douglas H; Zielinska, Barbara; Chow, Judith C; Kumar, Naresh

    2005-07-01

    The ratio of organic mass (OM) to organic carbon (OC) in PM(2.5) aerosols at US national parks in the IMPROVE network was estimated experimentally from solvent extraction of sample filters and from the difference between PM(2.5) mass and chemical constituents other than OC (mass balance) in IMPROVE samples from 1988 to 2003. Archived IMPROVE filters from five IMPROVE sites were extracted with dichloromethane (DCM), acetone and water. The extract residues were weighed to determine OM and analyzed for OC by thermal optical reflectance (TOR). On average, successive extracts of DCM, acetone, and water contained 64%, 21%, and 15%, respectively, of the extractable OC, respectively. On average, the non-blank-corrected recovery of the OC initially measured in these samples by TOR was 115+/-42%. OM/OC ratios from the combined DCM and acetone extracts averaged 1.92 and ranged from 1.58 at Indian Gardens, AZ in the Grand Canyon to 2.58 at Mount Rainier, WA. The average OM/OC ratio determined by mass balance was 2.07 across the IMPROVE network. The sensitivity of this ratio to assumptions concerning sulfate neutralization, water uptake by hygroscopic species, soil mass, and nitrate volatilization were evaluated. These results suggest that the value of 1.4 for the OM/OC ratio commonly used for mass and light extinction reconstruction in IMPROVE is too low.

  11. Forecasting Plant Productivity and Health Using Diffuse-to-Global Irradiance Ratios Extracted from the OMI Aerosol Product

    NASA Technical Reports Server (NTRS)

    Knowlton, Kelly; Andrews, Jane C.; Ryan, Robert E.

    2007-01-01

    Atmospheric aerosols are a major contributor to diffuse irradiance. This Candidate Solution suggests using the OMI (Ozone Monitoring Instrument) aerosol product as input into a radiative transfer model, which would calculate the ratio of diffuse to global irradiance at the Earth s surface. This ratio can significantly influence the rate of photosynthesis in plants; increasing the ratio of diffuse to global irradiance can accelerate photosynthesis, resulting in greater plant productivity. Accurate values of this ratio could be useful in predicting crop productivity, thereby improving forecasts of regional food resources. However, disagreements exist between diffuse-to-global irradiance values measured by different satellites and ground sensors. OMI, with its unique combination of spectral bands, high resolution, and daily global coverage, may be able to provide more accurate aerosol measurements than other comparable sensors.

  12. Externally mixed aerosol : simulation of ice nucleation in a parcel model

    NASA Astrophysics Data System (ADS)

    Anquetil-Deck, Candy; Hoose, Corinna; Conolly, Paul

    2014-05-01

    The effect of different aerosol (mineral dust, bacteria and soot) acting as immersion ice nuclei is investigated using ACPIM (AerosolCloud Precipitation Interaction Model) [1]. ACPIM is a powerful tool which can be used in two different ways. This box model can be, either, driven by experimental data (experiments carried out at the AIDA cloud chamber facility) or used as an air parcel in order to examine different ice nucleation parameterizations under specific conditions. This adiabatic air parcel model was employed for the simulation of a convective cloud. The study consists here in the investigation of how two externally mixed aerosols interact with one another. The initial study concentrates on mineral dust aerosol and biological aerosol without any background in order to fully understand the interaction between the different types of aerosol. Immersion freezing is described for the mineral dust aerosol by Niemand et al. 's parameterization [2], which was derived from laboratory studies in AIDA and is an extension of surface site density approach suggested by Connolly et al. [1]. Regarding bioaerosol, we introduce Hummel et al. 's parameterization [3] : f(in) = f(max)(1 - exp(- Ap *n(s)(T))) With an empirically fitted ice nucleation active site density n s based on AIDA measurements of Pseudomonas syringae bacteria [4]. This initial study is conducted for different proportion of each aerosol (the total number of aerosol being constant throughout all the simulation runs) at different vertical velocities. We then extented this study with different backgrounds (urban, marine, rural) in order to get a full picture. We found that there is not only a CCN competition but an IN competition as well. References : [1] Connolly, P. J., Möhler O., Field P. R., Saathoff H., Burgess, R., Choularton, T. and Gallagher, M., Atmos. Chem. Phys 9, 2805-2824 (2009). [2] Niemand, M., Möhler, O., Vogel B., Vogel, H., Hoose, C., Connolly, P., Klein, H., Bingemer, H., De

  13. Parameterization retrieval of trace gas volume mixing ratios from Airborne MAX-DOAS

    NASA Astrophysics Data System (ADS)

    Dix, Barbara; Koenig, Theodore K.; Volkamer, Rainer

    2016-11-01

    We present a parameterization retrieval of volume mixing ratios (VMRs) from differential slant column density (dSCD) measurements by Airborne Multi-AXis Differential Optical Absorption Spectroscopy (AMAX-DOAS). The method makes use of the fact that horizontally recorded limb spectra (elevation angle 0°) are strongly sensitive to the atmospheric layer at instrument altitude. These limb spectra are analyzed using reference spectra that largely cancel out column contributions from above and below the instrument, so that the resulting limb dSCDs, i.e., the column integrated concentration with respect to a reference spectrum, are almost exclusively sensitive to the atmospheric layers around instrument altitude. The conversion of limb dSCDs into VMRs is then realized by calculating box air mass factors (Box-AMFs) for a Rayleigh atmosphere and applying a scaling factor constrained by O4 dSCDs to account for aerosol extinction. An iterative VMR retrieval scheme corrects for trace gas profile shape effects. Benefits of this method are (1) a fast conversion that only requires the computation of Box-AMFs in a Rayleigh atmosphere; (2) neither local aerosol extinction nor the slant column density in the DOAS reference (SCDref) needs to be known; and (3) VMRs can be retrieved for every measurement point along a flight track, thus increasing statistics and adding flexibility to capture concentration gradients. Sensitivity studies are performed for bromine monoxide (BrO), iodine monoxide (IO) and nitrogen dioxide (NO2), using (1) simulated dSCD data for different trace gas and aerosol profiles and (2) field measurements from the Tropical Ocean tRoposphere Exchange of Reactive halogen species and Oxygenated VOC (TORERO) field experiment. For simulated data in a Rayleigh atmosphere, the agreement between the VMR from the parameterization method (VMRpara) and the true VMR (VMRtrue) is excellent for all trace gases. Offsets, slopes and R2 values for the linear fit of VMRpara over

  14. Characterization of the aerosol type using simultaneous measurements of the lidar ratio and estimations of the single scattering albedo

    NASA Astrophysics Data System (ADS)

    Amiridis, Vassilis; Balis, Dimitrios; Giannakaki, Eleni; Kazadzis, Stylianos; Arola, Antti; Gerasopoulos, Evangelos

    2011-07-01

    Lidar measurements of the vertical distribution of the aerosol extinction and backscatter coefficient and the corresponding extinction to backscatter ratio (so-called lidar ratio) at 355 nm have been performed at Thessaloniki, Greece using a Raman lidar system in the frame of the EARLINET for the period 2001-2005. Coincident spectral UV irradiance measurements, total ozone observations and aerosol optical depth estimates were available from a double Brewer spectroradiometer. The retrieval of single scattering albedo employed the Brewer global irradiance measurements and radiative transfer modeling. Vertically averaged values of the lidar ratio ranged from a minimum of 16 sr to a maximum value of 90 sr, while the effective single scattering albedo ranged from 0.78 to 1.00. The mean value of the lidar ratio for the dataset under study was 45.5 ± 21.0 sr while the average value of the single scattering albedo was 0.94 ± 0.05. For the majority of our measurements (80%) the single scattering albedo found to be greater than 0.90. Using additional information from backward trajectory calculations and lidar-derived free tropospheric contribution of aerosols in the columnar aerosol optical depth, it is shown that the combined use of the directly measured lidar ratio, and the indirectly estimated single scattering albedo, leads to a better characterization of the aerosol type probed.

  15. Aerosols

    Atmospheric Science Data Center

    2013-04-17

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

  16. Surface tensions, viscosities, and diffusion constants in mixed component single aerosol particles

    NASA Astrophysics Data System (ADS)

    Bzdek, Bryan; Marshall, Frances; Song, Young-Chul; Haddrell, Allen; Reid, Jonathan

    2016-04-01

    Surface tension and viscosity are important aerosol properties but are challenging to measure on individual particles owing to their small size and mass. Aerosol viscosity impacts semivolatile partitioning from the aerosol phase, molecular diffusion in the bulk of the particle, and reaction kinetics. Aerosol surface tension impacts how particles activate to serve as cloud condensation nuclei. Knowledge of these properties and how they change under different conditions hinders accurate modelling of aerosol physical state and atmospheric impacts. We present measurements made using holographic optical tweezers to directly determine the viscosity and surface tension of optically trapped droplets containing ~1-4 picolitres of material (corresponding to radii of ~5-10 micrometres). Two droplets are captured in the experimental setup, equilibrated to a relative humidity, and coalesced through manipulation of the relative trap positions. The moment of coalescence is captured using camera imaging as well as from elastically backscattered light connected to an oscilloscope. For lower viscosity droplets, the relaxation in droplet shape to a sphere follows the form of a damped oscillator and gives the surface tension and viscosity. For high viscosity droplets, the relaxation results in a slow merging of the two droplets to form a sphere and the timescale of that process permits determination of viscosity. We show that droplet viscosity and surface tension can be quantitatively determined to within <10% of the expected value for low viscosity droplets and to better than 1 order of magnitude for high viscosity droplets. Examples illustrating how properties such as surface tension can change in response to environmental conditions will be discussed. Finally, a study of the relationship between viscosity, diffusion constants, vapour pressures, and reactive uptake coefficients for a mixed component aerosol undergoing oxidation and volatilisation will be discussed.

  17. Effects of Iron Sand Ratios on the Basic Characteristics of Vanadium Titanium Mixed Ores

    NASA Astrophysics Data System (ADS)

    Liu, Dong-hui; Zhang, Jian-liang; Liu, Zheng-jian; Wang, Yao-zu; Xue, Xun; Yan, Jie

    2016-09-01

    Effects of iron sand ratios on the basic characteristics of vanadium titanium mixed ores were investigated using micro-sinter and grey relational analysis methods. The results show that iron sand presents poor assimilability, poor liquid flow capability, and low bonding phase strength. As the iron sand ratio in vanadium titanium mixed ores increases, the mixed ore's assimilation temperature increases, the fluidity index of liquid decreases, and the bonding phase strength first rises and then decreases. The comprehensive index of basic characteristic (CI) improves and then deteriorates with increasing iron sand ratio. The CI of vanadium titanium mixed ores is optimized when the iron sand ratio is 9 wt.%. In order to make full use of low-price iron-bearing materials and improve the sintering characteristics of vanadium titanium magnetite, the iron sand ratio in vanadium titanium mixed ores should be controlled within 9-12 wt.%.

  18. Organic aerosol emission ratios from the laboratory combustion of biomass fuels

    NASA Astrophysics Data System (ADS)

    Jolleys, Matthew D.; Coe, Hugh; McFiggans, Gordon; McMeeking, Gavin R.; Lee, Taehyoung; Kreidenweis, Sonia M.; Collett, Jeffrey L.; Sullivan, Amy P.

    2014-11-01

    Organic aerosol (OA) emission ratios (ER) have been characterized for 67 burns during the second Fire Laboratory at Missoula Experiment. These fires involved 19 different species representing 6 major fuels, each of which forms an important contribution to the U.S. biomass burning inventory. Average normalized ΔOA/ΔCO ratios show a high degree of variability, both between and within different fuel types and species, typically exceeding differen-ces between separate plumes in ambient measurements. This variability is strongly influenced by highly contrasting ΔOA levels between burns and the increased partitioning of semivolatile organic compounds to the particle phase at high ΔOA concentrations. No correlation across all fires was observed between ΔOA/ΔCO and modified combustion efficiency (MCE), which acts as an indicator of the proportional contributions of flaming and smoldering combustion phases throughout each burn. However, a negative correlation exists with MCE for some coniferous species, most notably Douglas fir, for which there is also an influence from fuel moisture content. 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 measured by aerosol mass spectrometer provides an indication of oxygenation as influenced by combustion processes at source, with ΔOA/ΔCO decreasing with increasing f44 for all fuel types. Inconsistencies in the magnitude of the effects associated with each potential influence on ΔOA/ΔCO emphasize the lack of a single dominant control on fire emissions, and a dependency on both fuel properties and combustion conditions.

  19. Application of a mixing-ratios based formulation to model mixing-driven dissolution experiments

    NASA Astrophysics Data System (ADS)

    Guadagnini, Alberto; Sanchez-Vila, Xavier; Saaltink, Maarten W.; Bussini, Michele; Berkowitz, Brian

    2009-05-01

    We address the question of how one can combine theoretical and numerical modeling approaches with limited measurements from laboratory flow cell experiments to realistically quantify salient features of complex mixing-driven multicomponent reactive transport problems in porous media. Flow cells are commonly used to examine processes affecting reactive transport through porous media, under controlled conditions. An advantage of flow cells is their suitability for relatively fast and reliable experiments, although measuring spatial distributions of a state variable within the cell is often difficult. In general, fluid is sampled only at the flow cell outlet, and concentration measurements are usually interpreted in terms of integrated reaction rates. In reactive transport problems, however, the spatial distribution of the reaction rates within the cell might be more important than the bulk integrated value. Recent advances in theoretical and numerical modeling of complex reactive transport problems [De Simoni M, Carrera J, Sanchez-Vila X, Guadagnini A. A procedure for the solution of multicomponent reactive transport problems. Water Resour Res 2005;41:W11410. doi: 10.1029/2005WR004056, De Simoni M, Sanchez-Vila X, Carrera J, Saaltink MW. A mixing ratios-based formulation for multicomponent reactive transport. Water Resour Res 2007;43:W07419. doi: 10.1029/2006WR005256] result in a methodology conducive to a simple exact expression for the space-time distribution of reaction rates in the presence of homogeneous or heterogeneous reactions in chemical equilibrium. The key points of the methodology are that a general reactive transport problem, involving a relatively high number of chemical species, can be formulated in terms of a set of decoupled partial differential equations, and the amount of reactants evolving into products depends on the rate at which solutions mix. The main objective of the current study is to show how this methodology can be used in conjunction

  20. The mixing state of carbonaceous aerosol particles in northern and southern California measured during CARES and CalNex 2010

    SciTech Connect

    Cahill, John F.; Suski, Kaitlyn; Seinfeld, John H.; Zaveri, Rahul A.; Prather, Kimberly A.

    2012-11-21

    Carbonaceous aerosols impact climate directly by scattering and absorbing radiation, and hence play a major, although highly uncertain, role in global radiative forcing. Commonly, ambient carbonaceous aerosols are internally mixed with secondary species such as nitrate, sulfate, and ammonium, which influence their climate impacts through optical properties, hygroscopicity, and atmospheric lifetime. Aircraft-aerosol time-of-flight mass spectrometry (A-ATOFMS), which measures single-particle mixing state, was used to determine the fraction of organic and soot aerosols that were internally mixed and the variability of their mixing state in California during the Carbonaceous Aerosol and Radiative Effects Study (CARES) and the Research at the Nexus of Air Quality and Climate Change (CalNex) field campaigns in the late spring and early summer of 2010. Nearly 88% of all A-ATOFMS measured particles (100-1000 nm in diameter) were internally mixed with secondary species, with 96% and 75% of particles internally mixed with nitrate and/or sulfate in southern and northern California, respectively. Even though atmospheric particle composition in both regions was primarily influenced by urban sources, the mixing state was found to vary greatly, with nitrate and soot being the dominant species in southern California, and sulfate and organic carbon in northern California. Furthermore, mixing state varied temporally in northern California, with soot becoming the prevalent particle type towards the end of the study as regional pollution levels increased. The results from these studies demonstrate that the majority of ambient carbonaceous particles are internally mixed and are heavily influenced by secondary species that are most predominant in each region. Based on these findings, considerations of regionally dominant sources and secondary species, as well as temporal variations of aerosol physical and optical properties, will be required to obtain more accurate predictions of the

  1. The mixing state of carbonaceous aerosol particles in northern and southern California measured during CARES and CalNex 2010

    NASA Astrophysics Data System (ADS)

    Cahill, J. F.; Suski, K.; Seinfeld, J. H.; Zaveri, R. A.; Prather, K. A.

    2012-11-01

    Carbonaceous aerosols impact climate directly by scattering and absorbing radiation, and hence play a major, although highly uncertain, role in global radiative forcing. Commonly, ambient carbonaceous aerosols are internally mixed with secondary species such as nitrate, sulfate, and ammonium, which influences their optical properties, hygroscopicity, and atmospheric lifetime, thus impacting climate forcing. Aircraft-aerosol time-of-flight mass spectrometry (A-ATOFMS), which measures single-particle mixing state, was used to determine the fraction of organic and soot aerosols that are internally mixed and the variability of their mixing state in California during the Carbonaceous Aerosols and Radiative Effects Study (CARES) and the Research at the Nexus of Air Quality and Climate Change (CalNex) field campaigns in the late spring and early summer of 2010. Nearly 88% of all A-ATOFMS measured particles (100-1000 nm in diameter) were internally mixed with secondary species, with 96% and 75% of particles internally mixed with nitrate and/or sulfate in southern and northern California, respectively. Even though atmospheric particle composition in both regions was primarily influenced by urban sources, the mixing state was found to vary greatly, with nitrate and soot being the dominant species in southern California, and sulfate and organic carbon in northern California. Furthermore, mixing state varied temporally in northern California, with soot becoming the prevalent particle type towards the end of the study as regional pollution levels increased. The results from these studies demonstrate that the majority of ambient carbonaceous particles in California are internally mixed and are heavily influenced by secondary species that are most prevalent in the particular region. Based on these findings, considerations of regionally dominant sources and secondary species, as well as temporal variations of aerosol physical and optical properties, will be required to obtain more

  2. The mixing state of carbonaceous aerosol particles in Northern and Southern California measured during CARES and CalNex 2010

    NASA Astrophysics Data System (ADS)

    Cahill, J. F.; Suski, K.; Seinfeld, J. H.; Zaveri, R. A.; Prather, K. A.

    2012-07-01

    Carbonaceous aerosols impact climate directly by scattering and absorbing radiation, and hence play a major, although highly uncertain, role in global radiative forcing. Commonly, ambient carbonaceous aerosols are internally mixed with secondary species such as nitrate, sulfate, and ammonium, which influences their optical properties, hygroscopicity, and atmospheric lifetime, thus impacting climate forcing. Aircraft-aerosol time-of-flight mass spectrometry (A-ATOFMS), which measures single-particle mixing state, was used to determine the fraction of organic and soot aerosols that are internally mixed and the variability of their mixing state in California during the Carbonaceous Aerosols and Radiative Effects Study (CARES) and the Research at the Nexus of Air Quality and Climate Change (CalNex) field campaigns in the late spring and early summer of 2010. Nearly 88% of all A-ATOFMS measured particles (100-1000 nm in diameter) were internally mixed with secondary species, with 96% and 75% of particles internally mixed with nitrate and/or sulfate in Southern and Northern California, respectively. Even though atmospheric particle composition in both regions was primarily influenced by urban sources, the mixing state was found to vary greatly, with nitrate and soot being the dominant species in Southern California, and sulfate and organic carbon in Northern California. Furthermore, mixing state varied temporally in Northern California, with soot becoming the prevalent particle type towards the end of the study as regional pollution levels increased. The results from these studies demonstrate that the majority of ambient carbonaceous particles in California are internally mixed and are heavily influenced by secondary species that are most prevalent in the particular region. Based on these findings, considerations of regionally dominant sources and secondary species, as well as temporal variations of aerosol physical and optical properties, will be required to obtain more

  3. Measurement of mixed biomass burning and mineral dust aerosol in the thermal infrared

    NASA Astrophysics Data System (ADS)

    Koehler, C. H.; Trautmann, T.; Lindermeir, E.

    2009-03-01

    From January 19th to February 7th, 2008, we installed a Fourier transform infrared spectrometer (FTIR) at Praia Airport on the island of Santiago, Cape Verde. Our goal was to measure the combined radiative effect of biomass burning aerosol and mineral dust usually observed there during that time of the year, when mineral dust emerging from the Sahara mixes with biomass burning aerosol transported north-westwards from the Sahelian region. Our measurements were part of the Saharan Mineral Dwst Experiment 2 (SAMUM 2) funded by the German Research Foundation (DFG) as continuation of the SAMUM field experiment in Morocco in 2006. SAMUM 2 is a joint venture of several German research institutes and universities and included both ground based as well as airborne measurements with the DLR Falcon research aircraft. The ground based instrumentation included spectrometers for visible and thermal infrared downwelling radiation, sun photometers, LIDAR and particle impactors while the Falcon was equipped with LIDAR and several instruments for aerosol analysis and sample return. A comparison of the FTIR measurements with radiative transfer simulations yields the expected aerosol forcing in the atmospheric window region after application of a suitable calibration method.

  4. Detection of internally mixed Asian dust with air pollution aerosols using a polarization optical particle counter and a polarization-sensitive two-wavelength lidar

    NASA Astrophysics Data System (ADS)

    Sugimoto, Nobuo; Nishizawa, Tomoaki; Shimizu, Atsushi; Matsui, Ichiro; Kobayashi, Hiroshi

    2015-01-01

    East Asia is a unique region where mineral dust (Asian dust) sources are located near urban and industrial areas. Asian dust is often mixed with air pollution aerosols during transportation. It is important to understand the mixing states of Asian dust and other aerosols, because the effects on the environment and human health differ depending on the mixing state. We studied the mixing states of Asian dust using a polarization particle counter (POPC) that measures the forward scattering and the two polarization components of backscattering for single particles and a polarization-sensitive (532 nm) two-wavelength (1064 nm and 532 nm) lidar. We conducted the simultaneous observations using the POPC and the lidar in Seoul from March to December 2013 and captured the characteristics of pure Asian dust and internally mixed polluted Asian dust. POPC measurements indicated that the density of large particles was lower in polluted Asian dust that transported slowly over the polluted areas than in pure Asian dust that transported quickly from the dust source region. Moreover, the backscattering depolarization ratio was smaller for all particle sizes in polluted dust. The optical characteristics measured using the lidar were consistent with the POPC measurements. The backscattering color ratio of polluted dust was comparable to that of pure dust, but the depolarization ratio was lower for polluted dust. In addition, coarse non-spherical particles (Asian dust) almost always existed in the background, and the depolarization ratio had seasonal variation with a lower depolarization ratio in the summer. These results suggest background Asian dust particles are internally mixed in the summer.

  5. A combined particle trap/HTDMA hygroscopicity study of mixed inorganic/organic aerosol particles

    NASA Astrophysics Data System (ADS)

    Zardini, A. A.; Sjogren, S.; Marcolli, C.; Krieger, U. K.; Gysel, M.; Weingartner, E.; Baltensperger, U.; Peter, T.

    2008-03-01

    Atmospheric aerosols are often mixtures of inorganic and organic material. Organics can represent a large fraction of the total aerosol mass and are comprised of water-soluble and insoluble compounds. Increasing attention was paid in the last decade to the capability of mixed inorganic/organic aerosol particles to take up water (hygroscopicity). We performed hygroscopicity measurements of internally mixed particles containing ammonium sulfate and carboxylic acids (citric, glutaric, adipic acid) in parallel with an electrodynamic balance (EDB) and a hygroscopicity tandem differential mobility analyzer (HTDMA). The organic compounds were chosen to represent three distinct physical states. During hygroscopicity cycles covering hydration and dehydration measured by the EDB and the HTDMA, pure citric acid remained always liquid, adipic acid remained always solid, while glutaric acid could be either. We show that the hygroscopicity of mixtures of the above compounds is well described by the Zdanovskii-Stokes-Robinson (ZSR) relationship as long as the two-component particle is completely liquid in the ammonium sulfate/citric acid and in the ammonium sulfate/glutaric acid cases. However, we observe significant discrepancies compared to what is expected from bulk thermodynamics when a solid component is present. We explain this in terms of a complex morphology resulting from the crystallization process leading to veins, pores, and grain boundaries which allow for water sorption in excess of bulk thermodynamic predictions caused by the inverse Kelvin effect on concave surfaces.

  6. Two extreme types of mixing of dust with urban aerosols observed in Kosa particles: ‘After’ mixing and ‘on-the-way’ mixing

    NASA Astrophysics Data System (ADS)

    Suzuki, Issei; Igarashi, Yasuhito; Dokiya, Yukiko; Akagi, Tasuku

    2010-02-01

    Besides well-known episodic Kosa during spring, high concentrations of Ca 2+ in aerosols were observed early in summer as well as in the semi-continuous data of the aerosols at the summit of Mt. Fuji. We further analysed the data to study the chemical characteristics of the high calcium event during early summer. The back trajectory analyses of the event indicated that Ca was transported from arid and semi-arid regions (e.g. the Taklamakan desert) through the westerly-dominated troposphere higher than the height of the summit of Fuji. The amount of SO 42- was always equivalent to that of NH 4+ unlike the case of the normal Kosa period where SO 42- is in excess with respect to NH 4+. This shows the 'after' mixing of unreacted CaCO 3 of Kosa origin with (NH 4) 2SO 4, which was only realized by the downward injection of Kosa particles from higher altitudes to the air masses of different origin. In the case of normal Kosa, the air bearing Kosa particles passed through the polluted area to absorb unneutralized acids ('on-the-way' mixing), whereas in the case of the Kosa-like phenomena in summer, the acids from the polluted area have been neutralized by NH 4+ and become inactive before mixing with CaCO 3 ("after" mixing). We have simplified the chemistry of aerosols using their three major components, Ca 2+, SO 42- and NH 4+, and introduced a new triangle diagram with the three assumed end-members of CaCO 3, CaSO 4 and (NH 4) 2SO 4 to quantify the contribution of the 'after' mixing to the aerosols (AMI; 'after' mixing index). Based on the back trajectories of some high AMI cases, CaCO 3 in Kosa particles was transported through the middle troposphere (5000-7000 m) and descended to meet another air mass where SO 42- had been already neutralized by NH 3.

  7. 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.; Gilde, S.; Zhang, Y.; Dall'Osto, M.

    2014-04-01

    The use of co-located multiple spectroscopic techniques can provide detailed information on the atmospheric processes regulating aerosol chemical composition and mixing state. So far, field campaigns heavily equipped with aerosol mass spectrometers have been carried out mainly in large conurbations and in areas directly affected by their outflow, whereas lesser efforts have been dedicated to continental areas characterized by a less dense urbanization. We present here the results obtained in San Pietro Capofiume, which is located in a sparsely inhabited sector of the Po Valley, Italy. The experiment was carried out in summer 2009 in the framework of the EUCAARI project ("European Integrated Project on Aerosol, Cloud Climate Aerosol Interaction"). For the first time in Europe, six state-of-the-art techniques were used in parallel: (1) on-line TSI aerosol time-of-flight mass spectrometer (ATOFMS), (2) on-line Aerodyne high-resolution time-of-flight aerosol mass spectrometer (HR-TOF-AMS), (3) soot particle aerosol mass spectrometer (SP-AMS), (4) on-line high resolution time-of-flight mass spectrometer-thermal desorption aerosol gas chromatograph (HR-ToFMS-TAG), (5) off-line twelve-hour resolution proton nuclear magnetic resonance (H-NMR) spectroscopy, and (6) chemical ionization mass spectrometry (CIMS) for the analysis of gas-phase precursors of secondary aerosol. Data from each aerosol spectroscopic method were analysed individually following ad-hoc tools (i.e. PMF for AMS, Art-2a for ATOFMS). The results obtained from each techniques are herein presented and compared. This allows us to clearly link the modifications in aerosol chemical composition to transitions in air mass origin and meteorological regimes. Under stagnant conditions, atmospheric stratification at night and early morning hours led to the accumulation of aerosols produced by anthropogenic sources distributed over the Po Valley plain. Such aerosols include primary components such as black carbon (BC

  8. Use of stable carbon and nitrogen isotope ratios in size segregated aerosol particles for the O/I penetration evaluation

    NASA Astrophysics Data System (ADS)

    Garbaras, Andrius; Garbariene, Inga; Masalaite, Agne; Ceburnis, Darius; Krugly, Edvinas; Kvietkus, Kestutis; Remeikis, Vidmantas; Martuzevicius, Dainius

    2015-04-01

    Stable carbon and nitrogen isotope ratio are successfully used in the atmospheric aerosol particle source identification [1, 2], transformation, pollution [3] research. The main purpose of this study was to evaluate the penetration of atmospheric aerosol particles from outdoor to indoor using stable carbon and nitrogen isotope ratios. Six houses in Kaunas (Lithuania) were investigated during February and March 2013. Electrical low pressure impactor was used to measure in real time concentration and size distribution of outdoor aerosol particles. ELPI+ includes 15 channels covering the size range from 0.017 to 10.0 µm. The 25 mm diameter aluminium foils were used to collect aerosol particles. Gravimetric analysis of samples was made using microbalance. In parallel, indoor aerosol samples were collected with a micro-orifice uniform deposition impactor (MOUDI model 110), where the aerosol particles were separated with the nominal D50 cut-off sizes of 0.056, 0.1, 0.18,0.32,0.56, 1.0, 1.8, 3.2, 5.6, 10, 18 μm for impactor stages 1-11, respectively. The impactor was run at a flow rate of 30 L/min. Air quality meters were used to record meteorological conditions (temperature, relative humidity) during the investigated period. All aerosol samples were analyzed for total carbon (TC) and total nitrogen (TN) contents and their isotopic compositions using elemental analyzer (EA) connected to the stable isotope ratio mass spectrometer (IRMS). TC concentration in indoors ranged from 1.5 to 247.5 µg/m3. During the sampling period outdoors TN levels ranged from 0.1 to 10.9 µg/m3. The obtained outdoor δ13C(PM2.5) values varied from -24.21 to -26.3‰, while the δ15N values varied from 2.4 to 11.1 ‰ (average 7.2±2.5 ‰). Indoors carbonaceous aerosol particles were depleted in 13C compared to outdoors in all sampling sites. This depletion in δ13C varied from 0.1 to 3.2 ‰. We think that this depletion occurs due ongoing chemical reactions (oxidation) when aerosol

  9. Single point aerosol sampling: Evaluation of mixing and probe performance in a nuclear stack

    SciTech Connect

    Rodgers, J.C.; Fairchild, C.I.; Wood, G.O.

    1995-02-01

    Alternative Reference Methodologies (ARMs) have been developed for sampling of radionuclides from stacks and ducts that differ from the methods required by the U.S. EPA. The EPA methods are prescriptive in selection of sampling locations and in design of sampling probes whereas the alternative methods are performance driven. Tests were conducted in a stack at Los Alamos National Laboratory to demonstrate the efficacy of the ARMs. Coefficients of variation of the velocity tracer gas, and aerosol particle profiles were determined at three sampling locations. Results showed numerical criteria placed upon the coefficients of variation by the ARMs were met at sampling stations located 9 and 14 stack diameters from flow entrance, but not at a location that is 1.5 diameters downstream from the inlet. Experiments were conducted to characterize the transmission of 10 {mu}m aerodynamic equivalent diameter liquid aerosol particles through three types of sampling probes. The transmission ratio (ratio of aerosol concentration at the probe exit plane to the concentration in the free stream) was 107% for a 113 L/min (4-cfm) anisokinetic shrouded probe, but only 20% for an isokinetic probe that follows the EPA requirements. A specially designed isokinetic probe showed a transmission ratio of 63%. The shrouded probe performance would conform to the ARM criteria; however, the isokinetic probes would not.

  10. Airborne measurements of hygroscopicity and mixing state of aerosols in the planetary boundary layer during the PEGASOS campaigns

    NASA Astrophysics Data System (ADS)

    Rosati, Bernadette; Weingartner, Ernest; Gysel, Martin; Rubach, Florian; Mentel, Thomas; Baltensperger, Urs

    2014-05-01

    Aerosols interact directly with the incident solar radiation by scattering or absorbing the light. The optical properties of an aerosol particle can strongly be altered at enhanced relative humidity (RH). Depending on the particle's chemical composition, it can experience hygroscopic growth, leading to a change in size and index of refraction compared to the dry particle (Zieger et al., 2011). Besides, aerosols can exist in different mixing states which are usually divided into internal and external mixtures. If all particles of a certain size have the same chemical composition, they are described as internally mixed, whereas if particles of equal size have different chemical composition, they are defined as externally mixed. Depending on the mixture the hygroscopic behavior will change: internally mixed aerosols will grow uniformly with increasing RH, while the different substances in external mixtures will experience different growing behaviors leading to a mode-splitting or broadened size distribution. Laboratory studies are commonly performed at dry conditions but it is known that temperature and RH as well as chemical composition are changing with altitude (Morgan et al., 2010). This further leads to the conclusion that the in-situ measurements of optical properties at different heights are crucial for climate forcing calculations. Within the Pan-European Gas-Aerosols-climate interaction Study (PEGASOS) the white- light humidified optical particle spectrometer (WHOPS) was developed and installed on the Zeppelin to investigate changes of light scattering with regard to water uptake and altitude. This instrument firstly selects a dry monodisperse aerosol by its electrical mobility and then exposes it to a well-defined RH (typically 95%). Alternately, the dry and humidified particles are measured in a white-light optical particle spectrometer (WELAS). In this way it is possible to infer the effective index of refraction of the dry particles, their hygroscopic

  11. A numerical study of aerosol influence on mixed-phase stratiform clouds through modulation of the liquid phase

    NASA Astrophysics Data System (ADS)

    de Boer, G.; Hashino, T.; Tripoli, G. J.; Eloranta, E. W.

    2013-02-01

    Numerical simulations were carried out in a high-resolution two-dimensional framework to increase our understanding of aerosol indirect effects in mixed-phase stratiform clouds. Aerosol characteristics explored include insoluble particle type, soluble mass fraction, influence of aerosol-induced freezing point depression and influence of aerosol number concentration. Simulations were analyzed with a focus on the processes related to liquid phase microphysics, and ice formation was limited to droplet freezing. Of the aerosol properties investigated, aerosol insoluble mass type and its associated freezing efficiency was found to be most relevant to cloud lifetime. Secondary effects from aerosol soluble mass fraction and number concentration also alter cloud characteristics and lifetime. These alterations occur via various mechanisms, including changes to the amount of nucleated ice, influence on liquid phase precipitation and ice riming rates, and changes to liquid droplet nucleation and growth rates. Alteration of the aerosol properties in simulations with identical initial and boundary conditions results in large variability in simulated cloud thickness and lifetime, ranging from rapid and complete glaciation of liquid to the production of long-lived, thick stratiform mixed-phase cloud.

  12. A three-dimensional sectional representation of aerosol mixing state for simulating optical properties and cloud condensation nuclei

    SciTech Connect

    Ching, Ping Pui; Zaveri, Rahul A.; Easter, Richard C.; Riemer, Nicole; Fast, Jerome D.

    2016-05-27

    Light absorption by black carbon (BC) particles emitted from fossil fuel combustion depends on the how thickly they are coated with non-refractory species such as ammonium, sulfate, nitrate, organics, and water. The cloud condensation nuclei (CCN) activation property of a particle depends on its dry size and the hygroscopicities of all the individual species mixed together. It is therefore necessary to represent both size and mixing state of aerosols to reliably predict their climate-relevant properties in atmospheric models. Here we describe and evaluate a novel sectional framework in the Model for Simulating Aerosol Interactions and Chemistry, referred to as MOSAIC-mix, that represents the mixing state by resolving aerosol dry size (Ddry), BC dry mass fraction (wBC), and hygroscopicity (κ). Using ten idealized urban plume scenarios in which different types of aerosols evolve over 24 hours under a range of atmospherically relevant environmental conditions, we examine errors in CCN concentrations and optical properties with respect to a more explicit aerosol mixing state representation. We find that only a small number of wBC and κ bins are needed to achieve significant reductions in the errors, and propose a configuration consisting of 24 Ddry bins, 2 wBC bins, and 2 κ bins that gives 24-hour average errors of about 5% or less in CCN concentrations and optical properties, 3-4 times lower than those from size-only-resolved simulations. These results show that MOSAIC-mix is suitable for use in regional and global models to examine the effects of evolving aerosol mixing states on aerosol-radiation-cloud feedbacks.

  13. Aerosol Inflluence on Ice Nucleation via the Immersion Mode in Mixed-Phase Arctic Stratiform Clouds

    NASA Astrophysics Data System (ADS)

    de Boer, G.; Hashino, T.; Tripoli, G. J.; Eloranta, E. W.

    2009-12-01

    Mixed-phase stratiform clouds are commonly observed at high latitudes (e.g. Shupe et al., 2006; de Boer et al., 2009a). Herman and Goody (1976), as well as Curry et al. (1996) present summaries of Arctic cloud climatologies that show low altitude stratus frequencies of up to 70% during transitional seasons. In addition to their frequent occurrence, these clouds have significant impacts on the near-surface atmospheric radiative budget, with estimates of wintertime reductions in net surface cooling of 40-50 Wm-2 (Curry et al., 1996) due predominantly to liquid in the mixed-phase layer. Both observational and modeling studies (e.g. Harrington et al., 1999; Jiang et al., 2000; Shupe et al., 2008; Klein et al., 2008) show a strong connection between the amount of ice present and the lifetime of the liquid portion of the cloud layer. This is thought to occur via the Bergeron-Findeissen mechanism (Pruppacher and Klett, 1997) in which ice grows at the expense of liquid due to its lower saturation vapor pressure. Unfortunately, the mechanisms by which ice is nucleated within these mixed-phase layers are not yet fully understood, and therefore an accurate depiction of this process for mixed-phase stratiform clouds has not yet been characterized. The nucleation mechanisms that are active in a given environment are sensitive to aerosol properties. Insoluble particles are typically good nuclei for ice particle formation, while soluble particles are typically better at nucleating water droplets. Aerosol observations from the Arctic often show mixed aerosol particles that feature both soluble and insoluble mass (Leaitch et al., 1984). Soluble mass fractions for these particles have been shown to be high, with estimates of 60-80% and are often made up of sulfates (Zhou et al., 2001; Bigg and Leck, 2001). It is believed that a significant portion of this sulfate mass comes from dimethyl sulfide (DMS) production in the Arctic Ocean and subsequent atmospheric oxidation. Since these

  14. 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

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

    SciTech Connect

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

    2010-05-01

    Aerosol microphysics, chemical composition, and CCN concentrations were measured at the T0 urban supersite in Mexico City during Megacity Initiative: Local and Global Research Observations (MILAGRO) in March 2006. The aerosol size distribution and composition often showed strong diurnal variation associated with traffic emissions and aging of aerosols through coagulation and local photochemical production of secondary aerosol species. CCN concentrations (N{sub CCN}) are derived using Kohler theory from the measured aerosol size distribution and various simplified aerosol mixing state and chemical composition, and are compared to concurrent measurements at five supersaturations ranging from 0.11% to 0.35%. The influence of assumed mixing state on calculated N{sub CCN} is examined using both aerosols observed during MILAGRO and representative aerosol types. The results indicate that while ambient aerosols often consist of particles with a wide range of compositions at a given size, N{sub CCN} may be derived within {approx}20% assuming an internal mixture (i.e., particles at a given size are mixtures of all participating species, and have the identical composition) if great majority of particles has an overall {kappa} (hygroscopicity parameter) value greater than 0.1. For a non-hygroscopic particle with a diameter of 100 nm, a 3 nm coating of sulfate or nitrate is sufficient to increase its {kappa} from 0 to 0.1. The measurements during MILAGRO suggest that the mixing of non-hygroscopic primary organic aerosol (POA) and black carbon (BC) particles with photochemically produced hygroscopic species and thereby the increase of their {kappa} to 0.1 take place in a few hours during daytime. This rapid process suggests that during daytime, a few tens of kilometers away for POA and BC sources, N{sub CCN} may be derived with sufficient accuracy by assuming an internal mixture, and using bulk chemical composition. The rapid mixing also indicates that, at least for very active

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

    NASA Astrophysics Data System (ADS)

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

    2016-09-01

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

  17. Formation of secondary aerosols from gasoline vehicle exhaust when mixing with SO2

    NASA Astrophysics Data System (ADS)

    Liu, T.; Wang, X.; Hu, Q.; Deng, W.; Zhang, Y.; Ding, X.; Fu, X.; Bernard, F.; Zhang, Z.; Lü, S.; He, Q.; Bi, X.; Chen, J.; Sun, Y.; Yu, J.; Peng, P.; Sheng, G.; Fu, J.

    2016-01-01

    Sulfur dioxide (SO2) can enhance the formation of secondary aerosols from biogenic volatile organic compounds (VOCs), but its influence on secondary aerosol formation from anthropogenic VOCs, particularly complex mixtures like vehicle exhaust, remains uncertain. Gasoline vehicle exhaust (GVE) and SO2, a typical pollutant from coal burning, are directly co-introduced into a smog chamber, in this study, to investigate the formation of secondary organic aerosols (SOA) and sulfate aerosols through photooxidation. New particle formation was enhanced, while substantial sulfate was formed through the oxidation of SO2 in the presence of high concentration of SO2. Homogenous oxidation by OH radicals contributed a negligible fraction to the conversion of SO2 to sulfate, and instead the oxidation by stabilized Criegee intermediates (sCIs), formed from alkenes in the exhaust reacting with ozone, dominated the conversion of SO2. After 5 h of photochemical aging, GVE's SOA production factor revealed an increase by 60-200 % in the presence of high concentration of SO2. The increase could principally be attributed to acid-catalyzed SOA formation as evidenced by the strong positive linear correlation (R2 = 0.97) between the SOA production factor and in situ particle acidity calculated by the AIM-II model. A high-resolution time-of-flight aerosol mass spectrometer (HR-TOF-AMS) resolved OA's relatively lower oxygen-to-carbon (O : C) (0.44 ± 0.02) and higher hydrogen-to-carbon (H : C) (1.40 ± 0.03) molar ratios for the GVE / SO2 mixture, with a significantly lower estimated average carbon oxidation state (OSc) of -0.51 ± 0.06 than -0.19 ± 0.08 for GVE alone. The relative higher mass loading of OA in the experiments with SO2 might be a significant explanation for the lower SOA oxidation degree.

  18. Formation of secondary aerosols from gasoline vehicle exhausts when mixing with SO2

    NASA Astrophysics Data System (ADS)

    Liu, T.; Wang, X.; Hu, Q.; Deng, W.; Zhang, Y.; Ding, X.; Fu, X.; Bernard, F.; Zhang, Z.; Lü, S.; He, Q.; Bi, X.; Chen, J.; Sun, Y.; Yu, J.; Peng, P.; Sheng, G.; Fu, J.

    2015-09-01

    Sulfur dioxide (SO2) can enhance the formation of secondary aerosols from biogenic volatile organic compounds (VOCs), but its influence on secondary aerosol formation from anthropogenic VOCs, particularly complex mixtures like vehicle exhausts, is still poorly understood. Here we directly co-introduced gasoline vehicles exhausts (GVE) and SO2, a typical pollutant from coal burning, into a smog chamber to investigate the formation of secondary organic aerosols (SOA) and sulfate aerosols through photooxidation. In the presence of high concentration of SO2, new particle formation was enhanced while substantial sulfate was formed through the oxidation of SO2. The homogenous oxidation by OH radicals contributed a negligible fraction to the conversion of SO2 to sulfate, and instead the oxidation by stabilized Criegee intermediates (sCIs), formed from alkenes in the exhaust reacting with ozone, dominated the conversion of SO2. After 5 h of photochemical aging, GVE's SOA production factor revealed an increase by 60-200 % in the presence of high concentration of SO2. This increase could largely be attributed to acid-catalyzed SOA formation, which was evidenced by the strong positive linear correlation (R2 = 0.97) between the SOA production factor and in-situ particle acidity calculated by AIM-II model. A high-resolution time-of-flight aerosol mass spectrometer (HR-TOF-AMS) resolved OA's relatively lower oxygen-to-carbon (O : C) and higher hydrogen-to-carbon (H : C) molar ratios for the GVE/SO2 mixture, with a much lower estimated average carbon oxidation state (OSc) of -0.51 ± 0.06 than that of -0.19 ± 0.08 for GVE alone. The relative higher mass loading of OA in the experiments with SO2 might be the major reason for the lower oxidation degree of SOA.

  19. On the graphical extraction of multipole mixing ratios of nuclear transitions

    NASA Astrophysics Data System (ADS)

    Rezynkina, K.; Lopez-Martens, A.; Hauschild, K.

    2017-02-01

    We propose a novel graphical method for determining the mixing ratios δ and their associated uncertainties for mixed nuclear transitions. It incorporates the uncertainties on both the measured and the theoretical conversion coefficients. The accuracy of the method has been studied by deriving the corresponding probability density function. The domains of applicability of the method are carefully defined.

  20. Behavior of zonal mean aerosol extinction ratio and its relationship with zonal mean temperature during the winter 1978-1979 stratospheric warming

    NASA Technical Reports Server (NTRS)

    Wang, P.-H.; Mccormick, M. P.

    1985-01-01

    The behavior of the zonal mean aerosol extinction ratio in the lower stratosphere near 75 deg N and its relationship with the zonal mean temperature during the January-February 1979 stratospheric sudden warming have been investigated based on the satellite sensor SAM II (Stratospheric Aerosol Measurement) and auxiliary meteorological measurements. The results indicate that distinct changes in the zonal mean aerosol extinction ratio occurred during this stratospheric sudden warming. It is also found that horizontal eddy transport due to planetary waves may have played a significant role in determining the distribution of the zonal mean aerosol extinction ratio.

  1. Shapes of internally mixed hygroscopic aerosol particles after deliquescence, and their effect on light scattering

    NASA Astrophysics Data System (ADS)

    Adachi, Kouji; Freney, Evelyn J.; Buseck, Peter R.

    2011-07-01

    Hygroscopic aerosol particles change the magnitude of light scattering through condensation and evaporation of water vapor. We collected aerosol particles from two megacities and observed the particle shapes at various values of relative humidity (RH) using an environmental cell within a transmission electron microscope. Many Mexico City samples had sulfate particles that were embedded within weakly hygroscopic organic aerosol, whereas the Los Angeles samples mainly consisted of externally mixed sulfate particles. For the Mexico City samples, when the RH was increased in the microscope, only the sulfate parts deliquesced, but the entire particle did not become spherical, i.e., particles containing deliquescent phases do not necessarily become spherical upon deliquescence. This result conflicts with the assumption used in many models, i.e., that deliquesced particles become spherical. Using a discrete-dipole approximation to calculate light scattering of simulated particles that resemble the observed ones, we show that, for particles >1.0 μm, the spherical-shape assumption used in Mie theory underestimates the light scattering by ˜50%, with the exact value depending on the sizes and relative volumes of the constituent phases.

  2. Mixing state of ambient aerosols in Nanjing city by single particle mass spectrometry

    NASA Astrophysics Data System (ADS)

    Wang, Honglei; An, Junlin; Shen, Lijuan; Zhu, Bin; Xia, Li; Duan, Qing; Zou, Jianan

    2016-05-01

    To investigate the mixing state and size-resolved aerosol in Nanjing, measurements were carried out for the period 14th January-1st February 2013 by using a Single Particle Aerosol Mass Spectrometer (SPAMS). A total of 10,864,766 particles were sized with vacuum aerodynamic diameter (dva) in the range of 0.2-2.0 μm. Of which, 1,989,725 particles were successfully ionized. Aerosol particles employed for analyzing SPAMS data utilized 96% of the hit particles to identify 5 main particle groups. The particle classes include: K-rich particles (K-CN, K-Nitrate, K-Sulfate and K-Secondary), sodium particles, ammonium particles, carbon-rich particles (OC, EC and OCEC) and heavy-metal particles (Fe-Secondary, Pb-Nitrate, Cu-Mn-Secondary and V-Secondary). EC was the largest contributor with a fraction of 21.78%, followed by K-Secondary (17.87%), K-Nitrate (12.68%) and K-CN (11.25%). High particle level and high RH (relative humidity) are two important factors decreasing visibility in Nanjing. Different particle classes have distinct extinction effects. It anti-correlated well with visibility for the K-secondary, sodium, ammonium, EC, Fe-Secondary and K-Nitrate particles. The proportion of EC particles at 0.65-1.4 μm was up to 25% on haze days and was below 10% on clean days.

  3. Seasonal variability and long term trends of chlorofluorocarbon mixing ratios in the unsaturated zone.

    PubMed

    Santella, Nicholas; Schlosser, Peter; Smethie, William M; Ho, David T; Stute, Martin

    2006-07-15

    To investigate processes that might affect chlorofluorocarbon (CFC) mixing ratios at the water table, a time series was obtained of unsaturated zone soil gas CFCs to depths of ca. 4 m at a site near New York City (NYC). Observed CFC 11, 12, and 113 mixing ratios were lower in winter than expected from either a local, high-resolution time series or remote atmospheric mixing ratios. A diffusion model, which includes seasonal changes in soil temperature, moisture, and CFC solubility, reproduces to first order the observed soil gas mixing ratios for CFC 11 and 12. Underestimation by the model of the seasonal cycle of CFC 11 points to changing levels of sorption to soils due to seasonal changes in temperature as an additional cause of the cycle seen in CFC 11 mixing ratios in soil air. In the case of spring recharge, low CFC mixing ratios in soil air caused by increased solubility may result in low CFC 11 concentrations in groundwater and, when dating groundwater recharged before the 1990s with CFCs, older apparent ages by up to 4 years. Attempts to observe average atmospheric CFC levels from soil gas are also significantly hindered by these seasonal fluctuations. Our results indicate the importance of considering seasonal changes in soil temperature when making precise observations of even very moderately soluble gases in the unsaturated zone and shallow groundwater.

  4. Large-scale distribution of surface ozone mixing ratio in southern Mongolia: A survey

    NASA Astrophysics Data System (ADS)

    Meixner, F. X.; Behrendt, T.; Ermel, M.; Hempelmann, N.; Andreae, M. O.; Jöckel, P.

    2012-04-01

    For the first time, measurements of surface ozone mixing ratio have been performed from semi-arid steppe to arid/hyper-arid southern Mongolian Gobi desert. During 12-29 August 2009, ozone mixing ratio was continuously measured from a mobile platform (4x4 Furgon SUV). The survey (3060 km / 229171km2) started at the Mongolian capital Ulaan-Baatar (47.9582° N, 107.0190° E ), heading to south-west (Echin Gol, 43.2586° N, 99.0255° E), eastward to Dalanzadgad (43.6061° N, 104.4445° E), and finally back to Ulaan-Baatar. Ambient air was sampled (approx. 1 l/min) through a 4 m long PTFE-intake line along a forward facing boom mounted on the roof of a 4x4 Furgon SUV. Ozone mixing ratio has been measured by UV-spectroscopy using a mobile dual-cell ozone analyzer (model 205, 2BTechnologies, Boulder, U.S.A.). While ozone signals were measured every 5 seconds, 1 minute averages and standard deviations have been calculated on-line and stored into the data logger. The latter are used to identify and to discriminate against unrealistic low or high ozone mixing ratios which have been due to occasionally passing plumes of vehicle exhaust and/or biomass burning gases, as well as gasoline (at gas filling stations). Even under desert conditions, the temporal behaviour of ozone mixing ratio was characterized by considerable and regular diel variations. Minimum mixing ratios (15-25 ppb) occurred early in the morning (approx. 06:00 local), when surface depletion of ozone (by dry deposition) can not be compensated by supply from the free troposphere due to thermodynamic stability of the nocturnal boundary layer. Late in the afternoon (approx. 17:00 local), under conditions of a turbulently well mixed convective boundary layer, maximum ozone mixing ratios (45-55 ppb) were reached. Daily amplitudes of the diel cycle of ozone mixing ratio were in the order of 30 ppb (steppe), 20 ppb (arid desert), to approx. 5 ppb (hyper-arid Gobi desert (Shargyn Gobi)). Ozone surface measurements were

  5. Detection of Remarkably Low Isotopic Ratio of Iron in Anthropogenic Aerosols and Evaluation of its Contribution to the Surface Ocean

    NASA Astrophysics Data System (ADS)

    Kurisu, M.; Iizuka, T.; Sakata, K.; Uematsu, M.; Takahashi, Y.

    2015-12-01

    It has been reported that phytoplankton growth in the High Nutrient-Low Chlorophyll (HNLC) regions is limited by dissolved iron (DFe) concentration (e.g., Martin and Fitzwater, 1988). Aerosol is known as one of the dominant sources of DFe to the ocean and classified into two origins such as anthropogenic and natural. A series of recent studies showed that Fe in anthropogenic aerosols is more soluble than that in natural aerosols (Takahashi et al., 2013) and has lower isotopic ratio (Mead et al., 2013). However, the difference between Fe isotopic ratio (δ56Fe: [(56Fe/54Fe)sample/(56Fe/54Fe)IRMM-14]-1) of two origins reported in Mead et al. (2013) is not so large compared with the standard deviation. Therefore, the aim of this study is to determine Fe species and δ56Fe in anthropogenic aerosols more accurately and to evaluate its contribution to the ocean surface. Iron species were determined by X-ray absorption fine structure (XAFS) analysis, while δ56Fe in size-fractionated aerosols were measured by MC-ICP-MS (NEPTUNE Plus) after chemical separation using anion exchange resin. Dominant Fe species in the samples were, ferrihydrite, hematite, and biotite. It was also revealed that coarse particles contained a larger amount of biotite and that fine particles contained a larger amount of hematite, which suggested that anthropogenic aerosols were emitted during combustion processes. In addition, results of Fe isotopic ratio analysis suggested that δ56Fe of coarse particles were around +0.25‰, whereas that of fine particles were -0.5 ˜ -2‰, which was lower than the δ56Fe in anthropogenic aerosol by Mead et al. (2013). The size-fractionated sampling made it possible to determine the δ56Fe in anthropogenic aerosol. Soluble component in fine particles extracted by simulated rain water also showed much lower δ56Fe (δ56Fe = -3.9±0.12‰), suggesting that anthropogenic Fe has much lower isotopic ratio. The remarkably low δ56Fe may be caused by the

  6. A numerical study of aerosol influence on mixed-phase stratiform clouds through modulation of the liquid phase

    NASA Astrophysics Data System (ADS)

    de Boer, G.; Hashino, T.; Tripoli, G. J.; Eloranta, E. W.

    2012-08-01

    Numerical simulations were carried out in a high-resolution two dimensional framework to increase our understanding of aerosol indirect effects in mixed-phase stratiform clouds. Aerosol characteristics explored include insoluble particle type, soluble mass fraction, the influence of aerosol-induced freezing point depression and the influence of aerosol number concentration. These experiments were completed with an emphasis on the liquid phase, with droplet freezing the mechanism for ice production. Of the aerosol properties investigated, aerosol insoluble mass type and its associated freezing efficiency was found to be most relevant to cloud lifetime. Secondary effects from aerosol soluble mass fraction and number concentration also alter cloud characteristics and lifetime. These alterations occur via various mechanisms, including changes to the amount of nucleated ice, influence on liquid phase precipitation and ice riming rates, and changes to liquid droplet growth rates. Simulation of the same environment leads to large variability of cloud thickness and lifetime, ranging from rapid and complete glaciation of the cloud to the production of a long-lived, thick stratiform mixed-phase cloud. In the end, these processes are summarized into a diagram that includes internal feedback loops that act within the cloud system.

  7. A combined particle trap/HTDMA hygroscopicity study of mixed inorganic/organic aerosol particles

    NASA Astrophysics Data System (ADS)

    Zardini, A. A.; Sjogren, S.; Marcolli, C.; Krieger, U. K.; Gysel, M.; Weingartner, E.; Baltensperger, U.; Peter, T.

    2008-09-01

    Atmospheric aerosols are often mixtures of inorganic and organic material. Organics can represent a large fraction of the total aerosol mass and are comprised of water-soluble and insoluble compounds. Increasing attention was paid in the last decade to the capability of mixed inorganic/organic aerosol particles to take up water (hygroscopicity). We performed hygroscopicity measurements of internally mixed particles containing ammonium sulfate and carboxylic acids (citric, glutaric, adipic acid) in parallel with an electrodynamic balance (EDB) and a hygroscopicity tandem differential mobility analyzer (HTDMA). The organic compounds were chosen to represent three distinct physical states. During hygroscopicity cycles covering hydration and dehydration measured by the EDB and the HTDMA, pure citric acid remained always liquid, adipic acid remained always solid, while glutaric acid could be either. We show that the hygroscopicity of mixtures of the above compounds is well described by the Zdanovskii-Stokes-Robinson (ZSR) relationship as long as the two-component particle is completely liquid in the ammonium sulfate/glutaric acid system; deviations up to 10% in mass growth factor (corresponding to deviations up to 3.5% in size growth factor) are observed for the ammonium sulfate/citric acid 1:1 mixture at 80% RH. We observe even more significant discrepancies compared to what is expected from bulk thermodynamics when a solid component is present. We explain this in terms of a complex morphology resulting from the crystallization process leading to veins, pores, and grain boundaries which allow for water sorption in excess of bulk thermodynamic predictions caused by the inverse Kelvin effect on concave surfaces.

  8. Importance of aerosol composition, mixing state, and morphology for heterogeneous ice nucleation: A combined field and laboratory approach

    NASA Astrophysics Data System (ADS)

    Baustian, Kelly J.; Cziczo, Daniel J.; Wise, Matthew E.; Pratt, Kerri A.; Kulkarni, Gourihar; Hallar, A. Gannet; Tolbert, Margaret A.

    2012-03-01

    In this study chemical compositions of background aerosol and ice nuclei were examined through laboratory investigations using Raman spectroscopy and field measurements by single-particle mass spectrometry. Aerosol sampling took place at Storm Peak Laboratory in Steamboat Springs, Colorado (elevation of 3210 m). A cascade impactor was used to collect coarse-mode aerosol particles for laboratory analysis by Raman spectroscopy; the composition, mixing state, and heterogeneous ice nucleation activity of individual particles were examined. For in situ analysis of fine-mode aerosol, ice nucleation on ambient particles was observed using a compact ice nucleation chamber. Ice crystals were separated from unactivated aerosol using a pumped counterflow virtual impactor, and ice nuclei were analyzed using particle analysis by laser mass spectrometry. For both fine and coarse modes, the ice nucleating particle fractions were enriched in minerals and depleted in sulfates and nitrates, compared to the background aerosol sampled. The vast majority of particles in both the ambient and ice active aerosol fractions contained a detectable amount of organic material. Raman spectroscopy showed that organic material is sometimes present in the form of a coating on the surface of inorganic particles. We find that some organic-containing particles serve as efficient ice nuclei while others do not. For coarse-mode aerosol, organic particles were only observed to initiate ice formation when oxygen signatures were also present in their spectra.

  9. Effect of velocity ratio on plane mixing layer development - Influence of the splitter plate wake

    NASA Technical Reports Server (NTRS)

    Mehta, R. D.

    1991-01-01

    The effect of the velocity ratio on the approach of a plane mixing layer to self-similarity was investigated experimentally. In the experiment, plane mixing layers with velocity ratios 0.5, 0.6, 0.7, 0.8, and 0.9 were generated in a mixing-layer wind tunnel consisting of two individually driven legs, in which the two streams were allowed to merge at the sharp edge of a tappered splitter plate. The leg driven by the bigger blower was operated at a free-stream velocity in the test section of 21 m/s, while the flow speed in the other leg was varied to change the velocity ratio. For each velocity ratio, the mean flow- and turbulence measurements were carried out at eight streamwise locations. Results showed that, for velocity ratios between 0.5 and 0.7, self-similarity of the mixing layer was achieved, with the asymptotic states comparable; mixing layers with higher velocity ratios failed to achieve a self-similar state within the measurement domain.

  10. Saharan and Arabian Dust Aerosols: A Comparative Case Study of Lidar Ratio

    NASA Astrophysics Data System (ADS)

    Córdoba-Jabonero, Carmen; Sabbah, Ismail; Sorribas, Mar; Adame, José Antonio; Cuevas, Emilio; Sharifi, Faisal Al; Gil-Ojeda, Manuel

    2016-06-01

    This work presents a first comparative study of the Lidar Ratio (LR) values obtained for dust particles in two singular dust-influenced regions: the Canary Islands (Spain, close to the African coast in the North Atlantic Ocean), frequently affected by Saharan dust intrusions, and the Kuwait area (Arabian Peninsula) as usually influenced by Arabian dust storms. Synergetic lidar and sun-photometry measurements are carried out in two stations located in these particular regions for that purpose. Several dusty cases were observed during 2014 in both stations and, just for illustration, two specific dusty case studies have been selected and analyzed to be shown in this work. In general, mean LR values of 54 sr and 40 sr were obtained in these studies cases for Saharan and Arabian dust particles, respectively. Indeed, these results are in agreement with other studies performed for dust particles arriving from similar desert areas. In particular, the disparity found in Saharan and Arabian dust LR values can be based on the singular composition of the suspended dust aerosols over each station. These results can be useful for CALIPSO extinction retrievals, where a single LR value (40 sr) is assumed for pure dust particles independently on the dust source region.

  11. The Pagami Creek smoke plume after long-range transport to the upper troposphere over Europe - aerosol properties and black carbon mixing state

    NASA Astrophysics Data System (ADS)

    Dahlkötter, F.; Gysel, M.; Sauer, D.; Minikin, A.; Baumann, R.; Seifert, P.; Ansmann, A.; Fromm, M.; Voigt, C.; Weinzierl, B.

    2013-11-01

    During the CONCERT~2011 field experiment with the DLR research aircraft Falcon an enhanced aerosol layer with particle linear depolarization ratios of 6-8% at 532 nm has been observed at altitudes above 10 km over northeast Germany on 16 September 2011. Dispersion simulations with HYSPLIT suggest that the elevated aerosol layer originated from the pyro-convective Pagami Creek forest fire in Minnesota, USA. The 3-4 days old smoke plume has high total refractory black carbon (rBC) mass concentrations of 0.03-0.35 μg m-3 at standard temperature and pressure (stp) with rBC mass equivalent diameters predominantly smaller than 130 nm. Assuming a~core-shell particle structure, the BC cores exhibit very thick (median: 105-136 nm) BC-free coatings, which modify the radiative transfer through this layer. A large fraction of the BC-containing particles disintegrate while passing the laser beam of the Single Particle Soot Photometer (SP2). This is shown for the first time for high-altitude aerosol layers in this study, giving evidence for heterogeneous mixing structures and possibly modified light-scattering and light-absorbing properties of the particles. This case study estimates the rBC mass import from the Pagami Creek forest fire into the upper troposphere/lower stratosphere (UTLS) region (best estimate: 25 Mg BC). A comparison to black carbon emission rates from aviation underlines the relevance of the import of forest fire aerosol on the BC load in the UTLS region. Our detailed information on the microphysics and the mixing state of the BC forest fire aerosol layer will help to better understand and investigate its radiative impact.

  12. In vitro dissolution of respirable aerosols of industrial uranium and plutonium mixed-oxide nuclear fuels.

    PubMed

    Eidson, A F; Mewhinney, J A

    1983-12-01

    Dissolution characteristics of mixed-oxide nuclear fuels are important considerations for prediction of biological behavior of inhaled particles. Four representative industrial mixed-oxide powders were obtained from fuel fabrication enclosures. Studies of the dissolution of Pu, Am and U from aerosol particles of these materials in a serum simulant solution and in 0.1M HCl showed: (1) dissolution occurred at a rapid rate initially and slowed at longer times, (2) greater percentages of U dissolved than Pu or Am: with the dissolution rates of U and Pu generally reflecting the physical nature of the UO2-PuO2 matrix, (3) the temperature history of industrial mixed-oxides could not be reliably related to Pu dissolution except for a 3-5% increase when incorporated into a solid solution by sintering at 1750 degrees C, and (4) dissolution in the serum simulant agreed with the in vivo UO2 dissolution rate and suggested the dominant role of mechanical processes in PuO2 clearance from the lung. The rapid initial dissolution rate was shown to be related, in part, to an altered surface layer. The advantages and uses of in vitro solubility data for estimation of biological behavior of inhaled industrial mixed oxides, such as assessing the use of chelation therapy and interpretation of urinary excretion data, are discussed. It was concluded that in vitro solubility tests were useful, simple and easily applied to individual materials potentially inhaled by humans.

  13. Mixing and water-soluble characteristics of particulate organic compounds in individual urban aerosol particles

    NASA Astrophysics Data System (ADS)

    Li, Weijun; Shao, Longyi

    2010-01-01

    Particulate organic compounds (POCs) in the atmosphere can alter the morphology and hygroscopicity of inorganic particles by coagulation and mixing. Direct observations can illustrate the mixing of organic and inorganic particles. Compositions, mixing states, and morphologies of 360 aerosol particles from urban Beijing collected on transmission electron microscopy (TEM) grids with Si-O substrate were obtained using TEM coupled with energy-dispersive X ray spectrometry (TEM/EDX). The Si-O substrate used in this study allows TEM/EDX to detect carbonaceous particles internally mixed with inorganic particles. POCs were present in approximately 90% of the nitrate-coated mineral particles on both hazy and clear days. Approximately 73% of K- and S-rich particles contained organic coatings and organic inclusions/aggregations on hazy days, while 53% of S-rich particles on clear days during the Beijing Olympics contained only organic coatings. Water dialysis of individual particles indicated that the organic inclusions/aggregations in the K- and S-rich particles were insoluble in water but that POCs from the coatings of individual particles were soluble. The organic coatings on individual inorganic particles may influence their surface hygroscopicity and optical properties.

  14. Hygroscopicity of internally mixed multi-component aerosol particles of atmospheric relevance

    NASA Astrophysics Data System (ADS)

    Liu, Qifan; Jing, Bo; Peng, Chao; Tong, Shengrui; Wang, Weigang; Ge, Maofa

    2016-01-01

    The hygroscopic properties of two water-soluble organic compounds (WSOCs) relevant to urban haze pollution (phthalic acid and levoglucosan) and their internally mixtures with inorganic salts (ammonium sulfate and ammonium nitrate) are investigated using a hygroscopicity tandem differential mobility analyzer (H-TDMA) system. The multi-component particles uptake water gradually in the range 5-90% relative humidity (RH). The experimental results are compared with the thermodynamic model predictions. For most mixtures, Extended Aerosol Inorganic Model (E-AIM) predictions agree well with the measured growth factors. The hygroscopic growth of mixed particles can be well described by the Zdanovskii-Stokes-Robinson (ZSR) relation as long as the mixed particles are completely liquid. ZSR calculations underestimate the water uptake of mixed particles at moderate RH due to the partial dissolution of ammonium sulfate in the organic and ammonium nitrate solution in this RH region. The phase of ammonium nitrate in the initial dry particles changes dramatically with the composition of mixtures. The presence of organics in the mixed particles can inhibit the crystallization of ammonium nitrate during the drying process and results in water uptake at low RH (RH < 60%). These results demonstrate that certain representative WSOCs can substantially influence the hygroscopicity of inorganic salts and overall water uptake of particles.

  15. Along-strike magma mixing beneath mid-ocean ridges - Effects on isotopic ratios

    NASA Technical Reports Server (NTRS)

    Kenyon, P. M.; Turcotte, D. L.

    1987-01-01

    The effects of mixing processes on the isotopic variability of midocean ridge basalts are studied. The processes considered are porous flow dispersion and convective mixing in magma chambers. Porous flow dispersion is capable of mixing magmas over distances of only a few tens of meters. Convective mixing, on the other hand, is found to produce continuous magma chambers, where mixing is limited by convective processes, and for discontinuous chambers, where mixing is limited by chamber size. Preliminary comparison of the calculations with observations along the midocean ridges shows that the calculations are consistent with the existence of a correlation between bathymetry and isotopic ratio at long, but not at short, wavelengths. They are also capable of explaining a decrease in isotopic variability with increasing spreading rate.

  16. A smog chamber study coupling a photoionization aerosol electron/ion spectrometer to VUV synchrotron radiation: organic and inorganic-organic mixed aerosol analysis

    NASA Astrophysics Data System (ADS)

    Baeza-Romero, María Teresa; Gaie-Levrel, Francois; Mahjoub, Ahmed; López-Arza, Vicente; Garcia, Gustavo A.; Nahon, Laurent

    2016-07-01

    A reaction chamber was coupled to a photoionization aerosol time-of-flight mass spectrometer based on an electron/ion coincidence scheme and applied for on-line analysis of organic and inorganic-organic mixed aerosols using synchrotron tunable vacuum ultraviolet (VUV) photons as the ionization source. In this proof of principle study, both aerosol and gas phase were detected simultaneously but could be differentiated. Present results and perspectives for improvement for this set-up are shown in the study of ozonolysis ([O3] = 0.13-3 ppm) of α-pinene (2-3 ppm), and the uptake of glyoxal upon ammonium sulphate. In this work the ozone concentration was monitored in real time, together with the particle size distributions and chemical composition, the latter taking advantage of the coincidence spectrometer and the tuneability of the synchrotron radiation as a soft VUV ionization source.

  17. Transport and Mixing Patterns over Central California during the Carbonaceous Aerosol and Radiative Effects Study (CARES)

    SciTech Connect

    Fast, Jerome D.; Gustafson, William I.; Berg, Larry K.; Shaw, William J.; Pekour, Mikhail S.; Shrivastava, ManishKumar B.; Barnard, James C.; Ferrare, R.; Hostetler, Chris A.; Hair, John; Erickson, Matthew H.; Jobson, Tom; Flowers, Bradley; Dubey, Manvendra K.; Springston, Stephen R.; Pirce, Bradley R.; Dolislager, Leon; Pederson, J. R.; Zaveri, Rahul A.

    2012-02-17

    We describe the synoptic and regional-scale meteorological conditions that affected the transport and mixing of trace gases and aerosols in the vicinity of Sacramento, California during June 2010 when the Carbonaceous Aerosol and Radiative Effects Study (CARES) was conducted. The meteorological measurements collected by various instruments deployed during the campaign and the performance of the chemistry version of the Weather Research and Forecasting model (WRF-Chem) are both discussed. WRF-Chem was run daily during the campaign to forecast the spatial and temporal variation of carbon monoxide emitted from 20 anthropogenic source regions in California to guide aircraft sampling. The model is shown to reproduce the overall circulations and boundary-layer characteristics in the region, although errors in the upslope wind speed and boundary-layer depth contribute to differences in the observed and simulated carbon monoxide. Thermally-driven upslope flows that transported pollutants from Sacramento over the foothills of the Sierra Nevada occurred every afternoon, except during three periods when the passage of mid-tropospheric troughs disrupted the regional-scales flow patterns. The meteorological conditions after the passage of the third trough were the most favorable for photochemistry and likely formation of secondary organic aerosols. Meteorological measurements and model forecasts indicate that the Sacramento pollutant plume was likely transported over a downwind site that collected trace gas and aerosol measurements during 23 periods; however, direct transport occurred during only eight of these periods. The model also showed that emissions from the San Francisco Bay area transported by intrusions of marine air contributed a large fraction of the carbon monoxide in the vicinity of Sacramento, suggesting that this source likely affects local chemistry. Contributions from other sources of pollutants, such as those in the Sacramento Valley and San Joaquin Valley

  18. Transport and mixing patterns over Central California during the carbonaceous aerosol and radiative effects study (CARES)

    SciTech Connect

    Fast J. D.; Springston S.; Gustafson Jr., W. I.; Berg, L. K.; Shaw, W. J.; Pekour, M.; Shrivastava, M.; Barnard, J. C.; Ferrare, R. A.; Hostetler, C. A.; Hair, J. A.; Erickson, M.; Jobson, B. T.; Flowers, B.; Dubey, M. K.; Pierce, R. B.; Dolislager, L.; Pederson, J.; Zaveri, R. A.

    2012-02-17

    We describe the synoptic and regional-scale meteorological conditions that affected the transport and mixing of trace gases and aerosols in the vicinity of Sacramento, California during June 2010 when the Carbonaceous Aerosol and Radiative Effects Study (CARES) was conducted. The meteorological measurements collected by various instruments deployed during the campaign and the performance of the chemistry version of the Weather Research and Forecasting model (WRF-Chem) are both discussed. WRF-Chem was run daily during the campaign to forecast the spatial and temporal variation of carbon monoxide emitted from 20 anthropogenic source regions in California to guide aircraft sampling. The model is shown to reproduce the overall circulations and boundary-layer characteristics in the region, although errors in the upslope wind speed and boundary-layer depth contribute to differences in the observed and simulated carbon monoxide. Thermally-driven upslope flows that transported pollutants from Sacramento over the foothills of the Sierra Nevada occurred every afternoon, except during three periods when the passage of mid-tropospheric troughs disrupted the regional-scale flow patterns. The meteorological conditions after the passage of the third trough were the most favorable for photochemistry and likely formation of secondary organic aerosols. Meteorological measurements and model forecasts indicate that the Sacramento pollutant plume was likely transported over a downwind site that collected trace gas and aerosol measurements during 23 time periods; however, direct transport occurred during only eight of these periods. The model also showed that emissions from the San Francisco Bay area transported by intrusions of marine air contributed a large fraction of the carbon monoxide in the vicinity of Sacramento, suggesting that this source likely affects local chemistry. Contributions from other sources of pollutants, such as those in the Sacramento Valley and San Joaquin

  19. Children's preference for mixed- versus fixed-ratio schedules of reinforcement: A translational study of risky choice.

    PubMed

    Mullane, Michael P; Martens, Brian K; Baxter, Emily L; Steeg, Danica Ver

    2017-01-01

    Laboratory research has shown that when subjects are given a choice between fixed-ratio and bi-valued mixed-ratio schedules of reinforcement, preference typically emerges for the mixed-ratio schedule even with a larger ratio requirement. The current study sought to replicate and extend these findings to children's math problem completion. Using an ABCBC reversal design, four fourth-grade students were given the choice of completing addition problems reinforced on either a fixed-ratio 5 schedule or one of three mixed-ratio schedules; an equivalent mixed-ratio (1, 9) schedule, a mixed-ratio (1, 11) schedule with a 20% larger ratio requirement, and an equally lean mixed-ratio (5, 7) schedule without the small fixed-ratio 1 component. This was followed by a reversal back to the preceding phase in which preference for the mixed-ratio schedule had been observed, and a final reversal back to the mixed-ratio (5, 7) phase. Findings were consistent with previous research in that all children preferred the mixed-ratio (1, 9) schedule over the equivalent fixed-ratio 5 schedule. Preference persisted for the leaner mixed-ratio (1, 11) schedule for three of the four children. Indifference or preference for the fixed-ratio 5 alternative was observed in phases containing the mixed-ratio (5, 7) schedule. These results extend previous research on risky choice to children's math problem completion and highlight the importance of a small ratio component in the emergence of preference for bi-valued mixed-ratio schedules. Implications of these results for arranging reinforcement to increase children's academic responding are discussed.

  20. Study on optical and microphysical properties of mixed aerosols from lidar during the EMEP 2012 summer campaign at 45oN 26oE

    NASA Astrophysics Data System (ADS)

    Talianu, Camelia; Nicolae, Doina; Belegante, Livio; Marmureanu, Luminita

    2013-04-01

    Aerosols optical and chemical properties in the upper layers of the atmosphere and near ground are variable, as function of the different mixtures of aerosol components resulting from their origin and transport over polluted areas. Due to a complex dynamics of air masses, the Romanian atmosphere has strong influences from dust and biomass-burning transported from South, West or East Europe. The dominant transport, and consequently the dominant aerosol type, depends on the season. As a result of the transport distance from the source and depending on the chemical and physical characteristics of the particles, tropospheric aerosols detected at Magurele, Romania, show different optical and microphysical properties than at the originating source. The differences are caused by the mixing with local particles, and also by the ageing processes and hygroscopic growth during the transport. This paper presents a statistical analysis of tropospheric aerosol optical properties during the EMEP (European Monitoring and Evaluation Programme) summer campaign (08 June - 17 July 2012), as retrieved from multiwavelength Raman and depolarization lidar data. Three elastic (1064, 532 and 355 nm), two Raman (607 and 387 nm) and one depolarization channel (532 nm parallel / 532 nm cross) are used to independently retrieve the backscatter coefficient, extinction coefficient and linear particle depolarization ratio of aerosols between 0.8 and 10 km altitude. Intensive optical parameters (Angstrom exponent, color ratios and color indexes) and microphysical parameters (effective radius, complex refractive index) from multiwavelength optical data inversion of the layer mean values are obtained. During the campaign, aerosol profiles were measured daily around sunset, following EARLINET standards. An intensive 3-days continuous measurements exercise was also performed. Layers were generally present above 2 km and bellow 6 km altitude, but descent of air masses from the free troposphere to the

  1. Very low isotope ratio of iron in fine aerosols related to its contribution to the surface ocean

    NASA Astrophysics Data System (ADS)

    Kurisu, Minako; Takahashi, Yoshio; Iizuka, Tsuyoshi; Uematsu, Mitsuo

    2016-09-01

    Seven size-fractionated aerosol samples were collected from Hiroshima, Japan, and were analyzed in terms of chemical composition, soluble fraction of iron (Fe), Fe species, and Fe isotope ratios. The results suggested that Fe in fine particles contained a larger fraction of anthropogenic aerosols than coarse particles did. Iron in the fine particles was more soluble in simulated seawater (up to 25%) than that in the coarse particles and was in the form of Fe (hydr)oxide species, such as ferrihydrite or hematite. The Fe isotope ratios (δ56Fe) of the coarse particles (+0.04‰ to +0.30‰) were close to the crustal mean value (0.0‰). By contrast, the δ56Fe values of fine particles were much lower and ranged from -2.01‰ to -0.56‰. δ56Fe values of the soluble Fe fraction in the fine particles were remarkably low (-3.91 to -1.87‰), suggesting that anthropogenic aerosols yield soluble Fe with low δ56Fe values. Such low values could be explained by kinetic isotope fractionation during evaporation of Fe at high temperatures, coupled with the refractory characteristics of Fe. Marine aerosols from the Northwest Pacific were also analyzed. The δ56Fe values in the fine particles were also lower than those in the coarse particles. These results may be important to quantitatively estimate the contribution of anthropogenic Fe deposited on the surface ocean on the basis of the Fe isotopes.

  2. Uptake of ozone to deliquesced KI and mixed KI/NaCl aerosol particles.

    PubMed

    Rouvière, Aurélie; Sosedova, Yulia; Ammann, Markus

    2010-07-08

    The kinetics of uptake of ozone to deliquesced potassium iodide (KI) aerosol particles has been investigated in an aerosol flow tube at 72-75% relative humidity, room temperature, and atmospheric pressure. The observed loss of ozone was further analyzed in terms of a numeric model to explicitly track the iodide concentration in the particles. This allowed retrieving a value alpha(b) = 0.6 +/- (0.5)(0.4) for the bulk accommodation coefficient (alpha(b)). The second order rate constant in the bulk phase agreed with available literature (k(b) = (1.0 +/- 0.3) x 10(9) M(-1) s(-1)) even for the high ionic strength conditions of the present experiments. As long as iodide remained in excess, the average uptake coefficient was gamma = (1.10 +/- 0.20) x 10(-2). Different experiments were performed where the iodide to chloride ratio, the ozone concentration, and the surface to volume ratio of particles were varied. In combination, the results obtained indicate that uptake was driven by fast bulk accommodation and reaction in the bulk for all conditions investigated. The results further suggest that ozone uptake is not limited by the bulk accommodation coefficient alpha(b) under atmospheric conditions.

  3. Mixing of Asian dust with pollution aerosol and the transformation of aerosol components during the dust storm over China in spring 2007

    NASA Astrophysics Data System (ADS)

    Huang, Kan; Zhuang, Guoshun; Li, Juan; Wang, Qiongzhen; Sun, Yele; Lin, Yanfen; Fu, Joshua S.

    2010-04-01

    An intensive spring aerosol sampling campaign over northwestern and northern China and a megacity in eastern China was conducted in the spring of 2007 to investigate the mixing of Asian dust with pollution aerosol during its long-range transport. On the basis of the results of the three sites near dust source regions (Tazhong, Yulin, and Duolun) and a metropolitan city (Shanghai), three dust sources, i.e., the western high-Ca dust in the Taklimakan Desert, the northwestern high-Ca dust and the northeastern low-Ca dust in Mongolia Gobi, were identified on the basis of the air mass trajectories and the elemental tracer analysis (e.g., Ca/Al, SO42-/S, Ca2+/Ca, and Na+/Na). The western dust was least polluted in comparison to the other two dust sources. The results evidently indicated that the dust could have already mixed with pollution aerosol even in near dust source regions. The concentrations of As, Cd, Cu, Pb, Zn, and S were elevated several times at all sites during dust days, showing the entrainment of pollution elements by dust. The secondary SO42- was observed to show much higher concentration due to the heterogeneous reaction on the alkaline dust during dust storm, while the concentrations of NO3- and NH4+ decreased owing to the dilution of the local pollution by the invaded dust. The western dust contained relatively low anthropogenic aerosols, and it mainly derived from the Taklimakan Desert, a paleomarine source. The northwestern dust had a considerable chemical reactivity and mixing with sulfur precursors emitted from the coal mines on the pathway of the long-range transport of dust. The northeastern dust reached Shanghai with high acidity, and it became the mixed aerosol with the interaction among dust, local pollutants, and sea salts. Comparison of the speciation of the water-soluble ions on both nondust and dust days at all sites illustrated the evolution of major ion species from different dust sources during the long-range transport of dust. The

  4. Stable Carbon Isotope Ratio of OC and TC in Aerosol Particles at Urban, Marine and Forest Sites

    NASA Astrophysics Data System (ADS)

    Masalaite, Agne; Dusek, Ulrike; Holzinger, Rupert; Röckmann, Thomas; Remeikis, Vidmantas

    2014-05-01

    Atmospheric aerosols contain up to 50 % (of) organic substances, thus substantially contributing to aerosol climate forcing and affecting human health. In addition to health and climate impacts, aerosol particulate matter is increasingly recognized for its role in biogeochemical cycles. δ13C value of carbonaceous aerosols is a useful tracer for distinguishing the origin of carbonaceous materials. Stable carbon isotope ratios were determined for organic carbon (OC) fraction and total carbon (TC) of PM1 collected on quartz fiber filters in Lithuania in March 2013 at three sites: the urban location of Vilnius, the coastal location of Preila and forest location of Rugsteliskis. The isotope values varied from -27.5 o to -25.5 o for OC and -27.9 o to -25.4 o for TC. δ13C values of TC of the marine site were depleted with some exceptions, at the forest site they were most enriched and the values of the city were in between. The city had the narrowest variation in TC indicating one main source of aerosol particles. The situation was different for OC values. δ13C values of the marine and the forest sites were relatively depleted, meanwhile the city site values were enriched and OC had a highest variability (1.6 o). The city samples had the best correlation (TC via OC). The marine values varied over a wide range (1.5 o) compared to the forest ones. The difference between TC and OC was not as high at the marine and city sites as at the forest site (the variation was about 5 times larger - the average OC was 1 o depleted). This indicates that VOC had a different origin than TC in the forest and in the city. Meanwhile marine aerosol particles had more or less the same source of OC and TC.

  5. Aerosol lidar observations of atmospheric mixing in Los Angeles: Climatology and implications for greenhouse gas observations.

    PubMed

    Ware, John; Kort, Eric A; DeCola, Phil; Duren, Riley

    2016-08-27

    Atmospheric observations of greenhouse gases provide essential information on sources and sinks of these key atmospheric constituents. To quantify fluxes from atmospheric observations, representation of transport-especially vertical mixing-is a necessity and often a source of error. We report on remotely sensed profiles of vertical aerosol distribution taken over a 2 year period in Pasadena, California. Using an automated analysis system, we estimate daytime mixing layer depth, achieving high confidence in the afternoon maximum on 51% of days with profiles from a Sigma Space Mini Micropulse LiDAR (MiniMPL) and on 36% of days with a Vaisala CL51 ceilometer. We note that considering ceilometer data on a logarithmic scale, a standard method, introduces, an offset in mixing height retrievals. The mean afternoon maximum mixing height is 770 m Above Ground Level in summer and 670 m in winter, with significant day-to-day variance (within season σ = 220m≈30%). Taking advantage of the MiniMPL's portability, we demonstrate the feasibility of measuring the detailed horizontal structure of the mixing layer by automobile. We compare our observations to planetary boundary layer (PBL) heights from sonde launches, North American regional reanalysis (NARR), and a custom Weather Research and Forecasting (WRF) model developed for greenhouse gas (GHG) monitoring in Los Angeles. NARR and WRF PBL heights at Pasadena are both systematically higher than measured, NARR by 2.5 times; these biases will cause proportional errors in GHG flux estimates using modeled transport. We discuss how sustained lidar observations can be used to reduce flux inversion error by selecting suitable analysis periods, calibrating models, or characterizing bias for correction in post processing.

  6. Increasing interannual and altitudinal ozone mixing ratios in the Catalan Pyrenees

    NASA Astrophysics Data System (ADS)

    Díaz-de-Quijano, Maria; Peñuelas, Josep; Ribas, Àngela

    2009-12-01

    Interannual, seasonal, daily and altitudinal patterns of tropospheric ozone mixing ratios, as well as ozone phytotoxicity and the relationship with NO x precursors and meteorological variables were monitored in the Central Catalan Pyrenees (Meranges valley and Forest of Guils) over a period of 5 years (2004-2008). Biweekly measurements using Radiello passive samplers were taken along two altitudinal transects comprised of thirteen stations ranging from 1040 to 2300 m a.s.l. Visual symptoms of ozone damage in Bel-W3 tobacco cultivars were evaluated biweekly for the first three years (2004-2006). High ozone mixing ratios, always above forest and vegetation protection AOT40 thresholds, were monitored every year. In the last 14 years, the AOT40 (Apr-Sept.) has increased significantly by 1047 μg m -3 h per year. Annual means of ozone mixing ratios ranged between 38 and 67 ppb v (38 and 74 ppb v during the warm period) at the highest site (2300 m) and increased at a rate of 5.1 ppb v year -1. The ozone mixing ratios were also on average 35-38% greater during the warm period and had a characteristic daily pattern with minimum values in the early morning, a rise during the morning and a decline overnight, that was less marked the higher the altitude. Whereas ozone mixing ratios increased significantly with altitude from 35 ppb v at 1040 m-56 ppb v at 2300 m (on average for 2004-2007 period), NO 2 mixing ratios decreased with altitude from 5.5 ppb v at 1040 m-1 ppb v at 2300 m. The analysis of meteorological variables and NO x values suggests that the ozone mainly originated from urban areas and was transported to high-mountain sites, remaining aloft in absence of NO. Ozone damage rates increased with altitude in response to increasing O 3 mixing ratios and a possible increase in O 3 uptake due to more favorable microclimatic conditions found at higher altitude, which confirms Bel-W3 as a suitable biomonitor for ozone concentrations during summer time. Compared to the

  7. Aerosol properties computed from aircraft-based observations during the ACE- Asia campaign. 2; A case study of lidar ratio closure and aerosol radiative effects

    NASA Technical Reports Server (NTRS)

    Kuzmanoski, Maja; Box, M. A.; Schmid, B.; Box, G. P.; Wang, J.; Russell, P. B.; Bates, D.; Jonsson, H. H.; Welton, Ellsworth J.; Flagan, R. C.

    2005-01-01

    For a vertical profile with three distinct layers (marine boundary, pollution and dust), observed during the ACE-Asia campaign, we carried out a comparison between the modeled lidar ratio vertical profile and that obtained from collocated airborne NASA AATS-14 sunphotometer and shipborne Micro-Pulse Lidar (MPL) measurements. Vertically resolved lidar ratio was calculated from two size distribution vertical profiles - one obtained by inversion of sunphotometer-derived extinction spectra, and one measured in-situ - combined with the same refractive index model based on aerosol chemical composition. The aerosol model implies single scattering albedos of 0.78 - 0.81 and 0.93 - 0.96 at 0.523 microns (the wavelength of the lidar measurements), in the pollution and dust layers, respectively. The lidar ratios calculated from the two size distribution profiles have close values in the dust layer; they are however, significantly lower than the lidar ratios derived from combined lidar and sunphotometer measurements, most probably due to the use of a simple nonspherical model with a single particle shape in our calculations. In the pollution layer, the two size distribution profiles yield generally different lidar ratios. The retrieved size distributions yield a lidar ratio which is in better agreement with that derived from lidar/sunphotometer measurements in this layer, with still large differences at certain altitudes (the largest relative difference was 46%). We explain these differences by non-uniqueness of the result of the size distribution retrieval and lack of information on vertical variability of particle refractive index. Radiative transfer calculations for this profile showed significant atmospheric radiative forcing, which occurred mainly in the pollution layer. We demonstrate that if the extinction profile is known then information on the vertical structure of absorption and asymmetry parameter is not significant for estimating forcing at TOA and the surface

  8. Effect of the HITRAN 92 spectral data on the retrieval of NO2 mixing ratios from Nimbus 7 LIMS

    NASA Technical Reports Server (NTRS)

    Remsburg, Ellis E.; Bhatt, Praful P.; Eckman, Richard S.; Gordley, Larry L.; Russell, James M., III; Siskind, David E.

    1994-01-01

    To ensure spectral consistency when comparing Nimbus 7 Limb Infrared Monitor of the Stratosphere Experiment (LIMS) NO2 distributions with those from Atmosphere Trace Molecule Spectroscopy (ATMOS) and Upper Atmosphere Research Satellite Experiments (UARS), 1 day (May 5, 1979) of LIMS measurements were reprocessed using the NO2 line list on the HITRAN 92 tape compiled by the Airforce Geophysics Laboratory (AFGL). The revised NO2 mixing ratios are smaller by up to 20%. The decrease is not constant with height, latitude, or time of day but depends on the absolute amount of NO2 in the profile, as a result of a change in the degree of saturation for the strong NO2 spectral lines. The revised NO2 agrees better with correlative measurements and with NO2 distributions from the Stratospheric Aerosol and Gas Experiment (SAGE) and Halogen Occultation Experiment (HALOE) satellite experiments but not with those from ATMOS 85. Profiles of the day/night ratio of revised NO2 are now larger near 5 hPa. There is also some improvement between observed and modeled ozone in the upper stratosphere, when the revised nighttime NO2 profile is used as the estimate of NO(y) for the model calculations.

  9. Effect of the HITRAN 92 spectral data on the retrieval of NO2 mixing ratios from Nimbus 7 LIMS

    NASA Astrophysics Data System (ADS)

    Remsburg, Ellis E.; Bhatt, Praful P.; Eckman, Richard S.; Gordley, Larry L.; Russell, James M., III; Siskind, David E.

    1994-11-01

    To ensure spectral consistency when comparing Nimbus 7 Limb Infrared Monitor of the Stratosphere Experiment (LIMS) NO2 distributions with those from Atmosphere Trace Molecule Spectroscopy (ATMOS) and Upper Atmosphere Research Satellite Experiments (UARS), 1 day (May 5, 1979) of LIMS measurements were reprocessed using the NO2 line list on the HITRAN 92 tape compiled by the Airforce Geophysics Laboratory (AFGL). The revised NO2 mixing ratios are smaller by up to 20%. The decrease is not constant with height, latitude, or time of day but depends on the absolute amount of NO2 in the profile, as a result of a change in the degree of saturation for the strong NO2 spectral lines. The revised NO2 agrees better with correlative measurements and with NO2 distributions from the Stratospheric Aerosol and Gas Experiment (SAGE) and Halogen Occultation Experiment (HALOE) satellite experiments but not with those from ATMOS 85. Profiles of the day/night ratio of revised NO2 are now larger near 5 hPa. There is also some improvement between observed and modeled ozone in the upper stratosphere, when the revised nighttime NO2 profile is used as the estimate of NO(y) for the model calculations.

  10. Particle-resolved simulation of aerosol size, composition, mixing state, and the associated optical and cloud condensation nuclei activation properties in an evolving urban plume

    SciTech Connect

    Zaveri, Rahul A.; Barnard, James C.; Easter, Richard C.; Riemer, Nicole; West, Matthew

    2010-09-11

    The recently developed particle-resolved aerosol box model PartMC-MOSAIC was used to simulate the evolution of aerosol mixing state and the associated optical and cloud condensation nuclei (CCN) activation properties in an idealized urban plume. The model explicitly resolved the size and composition of individual particles from a number of sources and tracked their evolution due to condensation/evaporation, coagulation, emission, and dilution. The ensemble black carbon (BC) specific absorption cross section increased by 40% over the course of two days as a result of BC aging by condensation and coagulation. Three- and four-fold enhancements in CCN/CN ratios were predicted to occur within 6 hours for 0.2% and 0.5% supersaturations (S), respectively. The particle-resolved results were used to evaluate the errors in the optical and CCN activation properties that would be predicted by a conventional sectional framework that assumes monodisperse, internally-mixed particles within each bin. This assumption artificially increased the ensemble BC specific absorption by 14-30% and decreased the single scattering albedo by 0.03-0.07 while the bin resolution had a negligible effect. In contrast, the errors in CCN/CN ratios were sensitive to the bin resolution, and they depended on the chosen supersaturation. For S = 0.2%, the CCN/CN ratio predicted using 100 internally-mixed bins was up to 25% higher than the particle-resolved results, while it was up to 125% higher using 10 internally-mixed bins. Errors introduced in the predicted optical and CCN properties by neglecting coagulation were also quantified.

  11. Effect of relative humidity on soot - secondary organic aerosol mixing: A case study from the Soot Aerosol Aging Study (PNNL-SAAS)

    NASA Astrophysics Data System (ADS)

    Sharma, N.; China, S.; Zaveri, R. A.; Shilling, J. E.; Pekour, M. S.; Liu, S.; Aiken, A. C.; Dubey, M. K.; Wilson, J. M.; Zelenyuk, A.; OBrien, R. E.; Moffet, R.; Gilles, M. K.; Gourihar, K.; Chand, D.; Sedlacek, A. J., III; Subramanian, R.; Onasch, T. B.; Laskin, A.; Mazzoleni, C.

    2014-12-01

    Atmospheric processing of fresh soot particles emitted by anthropogenic as well as natural sources alters their physical and chemical properties. For example, fresh and aged soot particles interact differently with incident solar radiation, resulting in different overall radiation budgets. Varying atmospheric chemical and meteorological conditions can result in complex soot mixing states. The Soot Aerosol Aging Study (SAAS) was conducted at the Pacific Northwest National Laboratory in November 2013 and January 2014 as a step towards understanding the evolution of mixing state of soot and its impact on climate-relevant properties. Aging experiments on diesel soot were carried out in a controlled laboratory chamber, and the effects of condensation and coagulation processes were systematically explored in separate sets of experiments. In addition to online measurement of aerosol properties, aerosol samples were collected for offline single particle analysis to investigate the evolution of the morphology, elemental composition and fine structure of sample particles from different experiments. Condensation experiments focused on the formation of α-pinene secondary organic aerosol on diesel soot aerosol seeds. Experiments were conducted to study the aging of soot under dry (RH < 2%) and humid conditions (RH ~ 80%). We present an analysis of the morphology of soot, its evolution, and its correlation with optical properties, as the condensation of α-pinene SOA is carried out for the two different RH conditions. The analysis was performed by using scanning electron microscopy, transmission electron microscopy, scanning transmission x-ray microscopy and atomic force microscopy for single particle characterization. In addition, particle size, mass, composition, shape, and density were characterized in-situ, as a function of organics condensed on soot seeds, using single particle mass spectrometer.

  12. Aerosol lidar observations of atmospheric mixing in Los Angeles: Climatology and implications for greenhouse gas observations

    NASA Astrophysics Data System (ADS)

    Ware, John; Kort, Eric A.; DeCola, Phil; Duren, Riley

    2016-08-01

    Atmospheric observations of greenhouse gases provide essential information on sources and sinks of these key atmospheric constituents. To quantify fluxes from atmospheric observations, representation of transport—especially vertical mixing—is a necessity and often a source of error. We report on remotely sensed profiles of vertical aerosol distribution taken over a 2 year period in Pasadena, California. Using an automated analysis system, we estimate daytime mixing layer depth, achieving high confidence in the afternoon maximum on 51% of days with profiles from a Sigma Space Mini Micropulse LiDAR (MiniMPL) and on 36% of days with a Vaisala CL51 ceilometer. We note that considering ceilometer data on a logarithmic scale, a standard method, introduces, an offset in mixing height retrievals. The mean afternoon maximum mixing height is 770 m Above Ground Level in summer and 670 m in winter, with significant day-to-day variance (within season σ = 220m≈30%). Taking advantage of the MiniMPL's portability, we demonstrate the feasibility of measuring the detailed horizontal structure of the mixing layer by automobile. We compare our observations to planetary boundary layer (PBL) heights from sonde launches, North American regional reanalysis (NARR), and a custom Weather Research and Forecasting (WRF) model developed for greenhouse gas (GHG) monitoring in Los Angeles. NARR and WRF PBL heights at Pasadena are both systematically higher than measured, NARR by 2.5 times; these biases will cause proportional errors in GHG flux estimates using modeled transport. We discuss how sustained lidar observations can be used to reduce flux inversion error by selecting suitable analysis periods, calibrating models, or characterizing bias for correction in post processing.

  13. Background NO/sub x/ mixing ratios in air masses over the North Atlantic ocean

    SciTech Connect

    Helas, G.; Warneck, P.

    1981-08-20

    A chemiluminescence analyzer was used to measure NO/sub x/ mixing ratios at the west coast of Ireland. Two measurement modes allowed the determination of NO and NO/sub x/ = NO+NO/sub 2/. In a third mode using a molybdenum converter, higher signals were observed than was in the second mode indicating that nitrogen compounds other than NO+NO/sub 2/ are registered. They are denoted 'excess NO/sub x/'. The average NO/sub 2/ mixing ratio for a week period was 101 +- 87 pptv. In pure marine air masses identified by means of trajectory calculations, the NO/sub 2/ mixing ratios were lower and exhibited in addition a diurnal variation with nighttime values of 37 +- 6 pptv and average values of 87 +- 47 pptv. Possible origins of the diurnal variation are discussed. For such conditions, the NO mixing ratio generally was unmeasurably small, certainly less than 10 pptv. The excess NO/sub x/ is also higher during the day compared with nighttime values of about 70 pptv. Further studies are required to identify the compounds involved.

  14. Impact of updated traffic emissions on HONO mixing ratios simulated for urban site in Houston, Texas

    NASA Astrophysics Data System (ADS)

    Czader, B. H.; Choi, Y.; Li, X.; Alvarez, S.; Lefer, B.

    2014-08-01

    Recent measurements in Houston show that HONO traffic emissions are 1.7% of NOx emissions which is about twice the previously estimated value of 0.8% based on tunnel measurements in 2001. The 0.8% value is widely used to estimate mobile emissions of HONO for air quality modeling applications. This study applies the newly estimated HONO/NOx ratio in the WRF-SMOKE-CMAQ modeling system and estimates the impact of higher HONO traffic emissions on its mixing ratios. Since applied emission inventory resulted in overestimates of NOx mixing ratios and because HONO emissions and chemical formation depends on the magnitude of NOx, thus, before proceeding with HONO emission modifications emissions of NOx were adjusted to reflect current emission trends. The modeled mixing ratios of NOx were evaluated against measured data from a number of sites in the Houston area. Overall, the NOx mean value dropped from 11.11 ppbv in the base case to 7.59 ppbv in the NOx adjusted case becoming much closer to the observed mean of 7.76 ppbv. The Index of Agreement (IOA) is improved in the reduced NOx case (0.71 vs. 0.75) and the Absolute Mean Error (AME) is lowered from 6.76 to 4.94. The modeled mixing ratios of HONO were evaluated against the actual observed values attained at the Moody Tower in Houston. The model could not reproduce the morning HONO peaks when the low HONO/NOx ratio of 0.008 was used to estimate HONO emissions. Doubling HONO emissions from mobile sources resulted in higher mixing ratios, the mean value increased from 0.30 to 0.41 ppbv becoming closer to the observed mean concentrations of 0.69 but still low; AME was slightly reduced from 0.46 to 0.43. IOA for simulation that used the 2001 emission values is 0.63 while for simulation with higher HONO emission it increased to 0.70. Increased HONO emissions impacted OH mixing ratio, up to about 6% increase was found during morning and mid-day hours. The impact on ozone is marginal. This study results sheds light on the

  15. Concentrations of iodine isotopes ((129)I and (127)I) and their isotopic ratios in aerosol samples from Northern Germany.

    PubMed

    Daraoui, A; Riebe, B; Walther, C; Wershofen, H; Schlosser, C; Vockenhuber, C; Synal, H-A

    2016-04-01

    New data about (129)I, (127)I concentrations and their isotopic ratios in aerosol samples from the trace survey station of the Physikalisch-Technische Bundesanstalt (PTB) in Braunschweig, Northern Germany, are presented and discussed in this paper. The investigated samples were collected on a weekly basis during the years 2011 to 2013. Iodine was extracted from aerosol filters using a strong basic solution and was separated from the matrix elements with chloroform and was analysed by accelerator mass spectrometry (AMS) for (129)I and by inductively coupled plasma mass spectrometry (ICP-MS) for (127)I. The concentrations of (127)I and (129)I in aerosol filters ranged from 0.31 to 3.71 ng m(-3) and from 0.06 to 0.75 fg m(-3), respectively. The results of (129)I/(127)I isotopic ratios were in the order 10(-8) to 10(-7). The (129)I originated directly from gaseous emissions and indirectly from liquid emissions (via sea spray) from the reprocessing plants in Sellafield and La Hague. In comparison with the results of (131)I after the Fukushima accident, no contribution of (129)I from this accident was detectable in Central Europe due to the high background originating from the (129)I releases of the European reprocessing plants. (129)I atmospheric activity concentrations were compared with those of an anthropogenic radionuclide ((85)Kr). We did not find any correlation between (129)I and (85)Kr, both having nuclear reprocessing plant as the main source.

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

    NASA Astrophysics Data System (ADS)

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

    2016-08-01

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

  17. Airborne In-Situ Measurements of Aerosol and Cloud Microphysical Properties in Mixed-Phase Clouds Under Varying Conditions

    NASA Astrophysics Data System (ADS)

    Comstock, J. M.; Fan, J.; Tomlinson, J. M.; Mei, F.; Hubbe, J. M.; Schmid, B.

    2014-12-01

    Cloud microphysical properties impact the interaction of clouds and radiation in the atmosphere, and can influence atmospheric circulations through changes in cloud phase. Characterizing the conditions that control phase changes and the microphysical properties of mixed-phase clouds is important for improving understanding of physical processes that influence cloud phase. We characterize the aerosol and cloud microphysical properties in relation to the atmospheric dynamic and thermodynamic conditions observed in mixed-phase clouds during several aircraft-based field experiments. The Department of Energy Atmospheric Radiation Measurement program's Gulfstream-1 aircraft was used to sample aerosol and cloud properties in warm and cold clouds during several recent field experiments. We analyze in-situ observations from the CalWater and TCAP field campaigns to examine the variability of cloud properties (phase, hydrometeor size, ice and liquid water content, particle habit) with changes in aerosol, vertical velocity, and temperature. These measurements indicate that in addition to aerosol concentration, vertical velocity strength has important influence on cloud phase in mixed-phase cloud regimes.

  18. Contact ratio of rough surfaces with multiple asperities in mixed lubrication at high pressures

    NASA Astrophysics Data System (ADS)

    Xiao, Huaping; Guo, Dan; Liu, Shuhai; Pan, Guoshun; Lu, Xinchun

    2012-02-01

    Relative optical intensity interference was used to measure the lubrication film thickness when four kinds of polyalphaolefin (PAO) were used as lubricants confined between a smooth sapphire disc surface and a rough steel ball surface. Maximum Hertz contact pressure up to 3 GPa was applied in the central part of the contact region in mixed lubrication. It was found that the contact ratio (the ratio of real contact region to the whole nominal contact region) is related to the film thickness, the applied pressure, the surface roughness and the rolling speed, and so on. Contact ratio evidently reduces as lubrication film thickness or rolling speed increases. Quantitative relationship between the contact ratio and the influence factors was summarized based on the nonlinear fitting of experimental measurements. A formula was put forward to calculate the contact ratio at high pressure conditions according to the current experimental results.

  19. Confidence interval of the likelihood ratio associated with mixed stain DNA evidence.

    PubMed

    Beecham, Gary W; Weir, Bruce S

    2011-01-01

    Likelihood ratios are necessary to properly interpret mixed stain DNA evidence. They can flexibly consider alternate hypotheses and can account for population substructure. The likelihood ratio should be seen as an estimate and not a fixed value, because the calculations are functions of allelic frequency estimates that were estimated from a small portion of the population. Current methods do not account for uncertainty in the likelihood ratio estimates and are therefore an incomplete picture of the strength of the evidence. We propose the use of a confidence interval to report the consequent variation of likelihood ratios. The confidence interval is calculated using the standard forensic likelihood ratio formulae and a variance estimate derived using the Taylor expansion. The formula is explained, and a computer program has been made available. Numeric work shows that the evidential strength of DNA profiles decreases as the variation among populations increases.

  20. Differences in Fine- Coarse Aerosol Ratios in Convective and Non-Convective Dust Events in a Desert City

    NASA Astrophysics Data System (ADS)

    Gill, T. E.; Rivera Rivera, N. I.; Novlan, D. J.

    2014-12-01

    El Paso, Texas (USA) and Ciudad Juarez, Chihuahua (Mexico) form the Paso del Norte, the largest metropolitan area in North America's Chihuahuan Desert. The cities are subject to frequent dust storms presenting a hazard to local infrastructure and health, including synoptic-scale dust events during winter and spring, and dusty outflows from convective storms (haboobs) primarily during the summer. We evaluate particulate matter (PM2.5 and PM10) concentrations over a decade of convective and non-convective dust events, based on hourly aerosol data collected by Texas Commission on Environmental Quality (TCEQ) continuous air monitors in El Paso cross-referenced to weather observations from the USA National Weather Service. A total of 219 dust events (95 convective and 124 non-convective) events occurred between 2001 and 2010. The PM2.5/PM10 ratio was significantly higher (proportionally greater concentration of fine aerosols) in convective episodes and during summertime events than during non-convective dust events and dust episodes in other seasons, although overall concentrations of both PM2.5 and PM10 were higher in the non-convective events, which were also longer-lasting. These differences in fine/coarse aerosol ratios are likely related to different atmospheric stability conditions, and/or different mechanisms of dust particle entrainment and transport in haboobs versus non-convective dust events. Since visibility degradation and adverse human health effects are known to be exacerbated by to fine aerosol concentrations, thunderstorm-related dust events may present a proportionally greater hazard.

  1. Surrogate/spent fuel sabotage aerosol ratio testing:phase 1 summary and results.

    SciTech Connect

    Vigil, Manuel Gilbert; Sorenson, Ken Bryce; Lange, F. , Germany); Nolte, O. (Fraunhofer Institut fur Toxikologie und Experimentelle Medizin, Germany); Koch, W. (Fraunhofer Institut fur Toxikologie und Experimentelle Medizin, Germany); Dickey, Roy R.; Yoshimura, Richard Hiroyuki; Molecke, Martin Alan; Autrusson, Bruno (Institut de Radioprotection et de Surete Nucleaire , France); Young, F. I.; Pretzsch, Gunter Guido (Gesellschaft fur Anlagen- und reaktorsicherheit , Germany)

    2005-10-01

    This multinational test program is quantifying the aerosol particulates produced when a high energy density device (HEDD) impacts surrogate material and actual spent fuel test rodlets. The experimental work, performed in four consecutive test phases, has been in progress for several years. The overall program provides needed data that are relevant to some sabotage scenarios in relation to spent fuel transport and storage casks, and associated risk assessments. This program also provides significant political benefits in international cooperation for nuclear security related evaluations. The spent fuel sabotage--aerosol test program is coordinated with the international Working Group for Sabotage Concerns of Transport and Storage Casks (WGSTSC), and supported by both the U.S. Department of Energy and Nuclear Regulatory Commission. This report summarizes the preliminary, Phase 1 work performed in 2001 and 2002 at Sandia National Laboratories and the Fraunhofer Institute, Germany, and documents the experimental results obtained, observations, and preliminary interpretations. Phase 1 testing included: performance quantifications of the HEDD devices; characterization of the HEDD or conical shaped charge (CSC) jet properties with multiple tests; refinement of the aerosol particle collection apparatus being used; and, CSC jet-aerosol tests using leaded glass plates and glass pellets, serving as representative brittle materials. Phase 1 testing was quite important for the design and performance of the following Phase 2 test program and test apparatus.

  2. Effect of Co/Ni ratios in cobalt nickel mixed oxide catalysts on methane combustion

    SciTech Connect

    Lim, Tae Hwan; Cho, Sung June; Yang, Hee Sung; Engelhard, Mark H.; Kim, Do Heui

    2015-07-31

    A series of cobalt nickel mixed oxide catalysts with the varying ratios of Co to Ni, prepared by co-precipitation method, were applied to methane combustion. Among the various ratios, cobalt nickel mixed oxides having the ratios of Co to Ni of (50:50) and (67:33) demonstrate the highest activity for methane combustion. Structural analysis obtained from X-ray diffraction (XRD) and extended X-ray absorption fine structure (EXAFS) evidently demonstrates that CoNi (50:50) and (67:33) samples consist of NiCo2O4and NiO phase and, more importantly, NiCo2O4spinel structure is largely distorted, which is attributed to the insertion of Ni2+ions into octahedral sites in Co3O4spinel structure. Such structural dis-order results in the enhanced portion of surface oxygen species, thus leading to the improved reducibility of the catalysts in the low temperature region as evidenced by temperature programmed reduction by hydrogen (H2TPR) and X-ray photoelectron spectroscopy (XPS) O 1s results. They prove that structural disorder in cobalt nickel mixed oxides enhances the catalytic performance for methane combustion. Thus, it is concluded that a strong relationship between structural property and activity in cobalt nickel mixed oxide for methane combustion exists and, more importantly, distorted NiCo2O4spinel structure is found to be an active site for methane combustion.

  3. Effect of jet-to-mainstream momentum flux ratio on mixing process

    NASA Astrophysics Data System (ADS)

    Gupta, Alka; Ibrahim, Mohamed Saeed; Amano, R. S.

    2016-03-01

    Temperature uniformity after a mixing process plays a very important role in many applications. Non-uniform temperature at the entrance of the turbine in gas turbine systems has an adverse effect on the life of the blades. These temperature non-uniformities cause thermal stresses in the blades leading to higher maintenance costs. This paper presents experimental and numerical results for mixing process in coaxial ducts. The effect of increased jet-to-mainstream momentum flux ratio on the temperature uniformity of the exit flow was analyzed. It was found that better mixing of primary (or hot) stream and dilution (or cold) stream was achieved at higher flux ratio. Almost 85 % of the equilibrium mixture fraction was achieved at flux ratio of 0.85 after which no significant improvement was achieved while the exergy destruction kept on increasing. A new parameter, `Cooling Rate Number', was defined to identify the potential sites for presence of cold zones within the mixing section. Parametric study reveals that the cooling rate numbers were higher near the dilution holes which may result in rapid cooling of the gases.

  4. Atmospheric mixing ratios of methyl ethyl ketone (2-butanone) in tropical, boreal, temperate and marine environments

    NASA Astrophysics Data System (ADS)

    Yáñez-Serrano, A. M.; Nölscher, A. C.; Bourtsoukidis, E.; Derstroff, B.; Zannoni, N.; Gros, V.; Lanza, M.; Brito, J.; Noe, S. M.; House, E.; Hewitt, C. N.; Langford, B.; Nemitz, E.; Behrendt, T.; Williams, J.; Artaxo, P.; Andreae, M. O.; Kesselmeier, J.

    2016-09-01

    Methyl ethyl ketone (MEK) enters the atmosphere following direct emission from vegetation and anthropogenic activities, as well as being produced by the gas-phase oxidation of volatile organic compounds (VOCs) such as n-butane. This study presents the first overview of ambient MEK measurements at six different locations, characteristic of forested, urban and marine environments. In order to understand better the occurrence and behaviour of MEK in the atmosphere, we analyse diel cycles of MEK mixing ratios, vertical profiles, ecosystem flux data, and HYSPLIT back trajectories, and compare with co-measured VOCs. MEK measurements were primarily conducted with proton-transfer-reaction mass spectrometer (PTR-MS) instruments. Results from the sites under biogenic influence demonstrate that vegetation is an important source of MEK. The diel cycle of MEK follows that of ambient temperature and the forest structure plays an important role in air mixing. At such sites, a high correlation of MEK with acetone was observed (e.g. r2 = 0.96 for the SMEAR Estonia site in a remote hemiboreal forest in Tartumaa, Estonia, and r2 = 0.89 at the ATTO pristine tropical rainforest site in central Amazonia). Under polluted conditions, we observed strongly enhanced MEK mixing ratios. Overall, the MEK mixing ratios and flux data presented here indicate that both biogenic and anthropogenic sources contribute to its occurrence in the global atmosphere.

  5. Aerosol black carbon characteristics over Central India: Temporal variation and its dependence on mixed layer height

    NASA Astrophysics Data System (ADS)

    Kompalli, Sobhan Kumar; Babu, S. Suresh; Moorthy, K. Krishna; Manoj, M. R.; Kumar, N. V. P. Kiran; Shaeb, K. Hareef Baba; Joshi, Ashok Kumar

    2014-10-01

    In a first of its kind study over the Indian region, concurrent and extensive measurements of black carbon (BC) concentration and atmospheric boundary layer parameters are used to quantify the role of atmospheric boundary layer in producing temporal changes in BC. During this study, 18 months (2011-12) data of continuous measurements of BC aerosols, made over a semi-urban location, Nagpur, in Central India are used along with concurrent measurements of vertical profiles of atmospheric thermodynamics, made using weekly ascents of GPS aided Radiosonde for a period of 1 year. From the balloon data, mixed layer heights and ventilation coefficients are estimated, and the monthly and seasonal changes in BC mass concentration are examined in the light of the boundary layer changes. Seasonally, the BC mass concentration was highest (~ 4573 ± 1293 ng m- 3) in winter (December-February), and lowest (~ 1588 ± 897 ng m- 3) in monsoon (June-September), while remained moderate (~ 3137 ± 1446 ng m- 3) in pre-monsoon (March-May), and post-monsoon (~ 3634 ± 813 ng m- 3) (October-November) seasons. During the dry seasons, when the rainfall is scanty or insignificantly small, the seasonal variations in BC concentrations have a strong inverse relationship with mixed layer height and ventilation coefficient. However, the lowest BC concentrations do not occur during the season when the mixed layer height (MLH) is highest or the ventilation coefficient is the highest; rather it occurs when the rainfall is strong (during summer monsoon season) and airmass changes to primarily of marine origin.

  6. Impact of updated traffic emissions on HONO mixing ratios simulated for urban site in Houston, Texas

    NASA Astrophysics Data System (ADS)

    Czader, B. H.; Choi, Y.; Li, X.; Alvarez, S.; Lefer, B.

    2015-02-01

    Recent measurements in Houston show that HONO traffic emissions are 1.7% of NOx emissions, which is about twice the previously estimated value of 0.8% based on tunnel measurements in 2001. The 0.8% value is widely used to estimate mobile emissions of HONO for air quality modeling applications. This study applies the newly estimated HONO / NOx ratio in the WRF-SMOKE-CMAQ modeling system and estimates the impact of higher HONO traffic emissions on its mixing ratios. Since applied emission inventory resulted in overestimates of NOx mixing ratios and because HONO emissions and chemical formation depend on the magnitude of NOx, thus, before proceeding with HONO emission modifications emissions of NOx were adjusted to reflect current emission trends. The modeled mixing ratios of NOx were evaluated against measured data from a number of sites in the Houston area. Overall, the NOx mean value dropped from 11.11 ppbv in the base case to 7.59 ppbv in the NOx-adjusted case becoming much closer to the observed mean of 7.76 ppbv. The index of agreement (IOA) is improved in the reduced NOx case (0.71 vs. 0.75) and the absolute mean error (AME) is lowered from 6.76 to 4.94. The modeled mixing ratios of HONO were evaluated against the actual observed values attained at the Moody Tower in Houston. The model could not reproduce the morning HONO peaks when the low HONO / NOx ratio of 0.008 was used to estimate HONO emissions. Doubling HONO emissions from mobile sources resulted in higher mixing ratios, and the mean value increased from 0.30 to 0.41 ppbv becoming closer to the observed mean concentrations of 0.69 but still low; AME was slightly reduced from 0.46 to 0.43. IOA for simulation that used the 2001 emission values is 0.63 while for simulation with higher HONO emission it increased to 0.70. Increased HONO emissions from mobile sources resulted in a 14% increase in OH during morning time at the location of the Moody Tower and 3% when averaged over an urban area. The increase

  7. Effects of specimen size and mix ratio on the nickel migration behavior of landfill waste mixed mortar.

    PubMed

    Haque, M Aminul

    2017-04-01

    Landfill solid waste management system poses the potential source of silent wide-spread heavy metals like nickel poisoning in the entire ecosystem of nearby environment. Nickel containing demolish solid wastes are disposed at landfill zones to a great extent from where nickel migrate into the food chain through the surface water body as well as groundwater. Consequently, nickel exposure may cause different environmental problems. From this sense, it may be an attractive proposal to recycle the waste as a sustainable product. Herein is presented a long-term feasibility study on potential leaching behavioral pattern of nickel from different sizes and mixes based solidified landfill waste mixed mortar block. The calculated results revealed the larger sizes block entrapped more nickel content than the smaller in relation to the available for leaching. Moreover, the specimen bearing the higher amount of waste resulted the significant nickel immobilization within the crystalline structure. The study observed the fixation results 97.72%-99.35%, 97.08%-99.11%, 96.19%-98.58% and 95.86%-91.6% under the stabilizing agent to fine aggregate mixing combination 1:1, 1:1.5, 1:2 and 1:2.5 respectively where 30% of the total volume of fine aggregate was replaced by landfill waste. Although, mechanical strength test of all surrogate waste forms was also conducted that showed acceptable performance for land disposal, the current research pointing out that constructed green products were non-hazardous except the specimens having mixture ratio 1:2.5 because nickel ion release mechanism was observed under this ratio by surface decay or physical erosion of the monolithic matrices. Furthermore, semi-empirical based dominant leaching mechanism models were justified against the goodness of fit statistical parameters for interpreting the experimental observations of nickel transport profile where the adopted models possessed strong potential for predicting Ni content with high accuracy.

  8. Effective Giromagnetic Ratios in Artifical Nuclear Magnetization Pumping of the Noble Gases Mix

    NASA Astrophysics Data System (ADS)

    Popov, E. N.; Barantsev, K. A.; Litvinov, A. N.

    2015-09-01

    Dynamic of the nuclear magnetization of the two noble gases mix was studied in this research. Nuclear magnetization pumped along the induction of external magnetic field. Vector of nuclear magnetization is given a tilt by the week rotational magnetic field, which makes NMR for noble gases. Interaction between the nuclear magnetic moments of the different noble gases adducted to shifts at the frequency of nuclear moments precession in external magnetic field. Effective gyromagnetic ratios of the nuclear of noble gases is defined and it different from the tabulated value. There is theoretical calculation of effective gyromagnetic ratios in this research.

  9. Calibration method for the lidar-observed stratospheric depolarization ratio in the presence of liquid aerosol particles.

    PubMed

    Adachi, H; Shibata, T; Iwasaka, Y; Fujiwara, M

    2001-12-20

    A fine calibration of the depolarization ratio is required for a detailed interpretation of lidar-observed polar stratospheric clouds. We propose a procedure for analyzing data by using atmospheric depolarization lidar. The method is based on a plot of deltaT versus (1 - RT(-1)), where deltaT is the total depolarization ratio and RT is the total backscattering ratio. Assuming that there are only spherical particles in some altitude ranges of the lidar data, the characteristics of the plot of deltaT versus (1 - RT(-1)) lead to a simple but effective calibration method for deltaT. Additionally, the depolarization of air molecules deltam can be determined in the process of deltaT calibration. We compared determined values with theoretically calculated values for the depolarization of air to test the proposed method. The deltam value was calculated from the lidar data acquired at Ny-Alesund (79 degrees N, 12 degrees E), Svalbard in winter 1994-1995. When only sulfate aerosols were present on 24 December 1994, deltam was 0.46 +/- 0.35%. When the particles consisted of sulfate aerosols and spherical particles of polar stratospheric clouds on 4 January 1995, deltam was 0.45 +/- 0.07%. Both deltam values were in good agreement with the theoretically calculated value, 0.50 +/- 0.03%.

  10. Increasing Springtime Ozone Mixing Ratios in the Free Troposphere Over Western North America

    NASA Technical Reports Server (NTRS)

    Cooper, O. R.; Parrish, D. D.; Stohl, A.; Trainer, M.; Nedelec, P.; Thouret, V.; Cammas, J. P.; Oltmans, S. J.; Johnson, B. J.; Tarasick, D.; Leblanc, T.; McDermid, I. S.; Jaffe, D.; Gao, R.; Stith, J.; Ryerson, T.; Aikin, K.; Campos, T.; Weinheimer, A.; Avery, M. A.

    2010-01-01

    In the lowermost layer of the atmosphere - the troposphere - ozone is an important source of the hydroxyl radical, an oxidant that breaks down most pollutants and some greenhouse gases. High concentrations of tropospheric ozone are toxic, however, and have a detrimental effect on human health and ecosystem productivity1. Moreover, tropospheric ozone itself acts as an effective greenhouse gas. Much of the present tropospheric ozone burden is a consequence of anthropogenic emissions of ozone precursors resulting in widespread increases in ozone concentrations since the late 1800s. At present, east Asia has the fastest-growing ozone precursor emissions. Much of the springtime east Asian pollution is exported eastwards towards western North America. Despite evidence that the exported Asian pollution produces ozone, no previous study has found a significant increase in free tropospheric ozone concentrations above the western USA since measurements began in the late 1970s. Here we compile springtime ozone measurements from many different platforms across western North America. We show a strong increase in springtime ozone mixing ratios during 1995-2008 and we have some additional evidence that a similar rate of increase in ozone mixing ratio has occurred since 1984. We find that the rate of increase in ozone mixing ratio is greatest when measurements are more heavily influenced by direct transport from Asia. Our result agrees with previous modelling studies, which indicate that global ozone concentrations should be increasing during the early part of the twenty-first century as a result of increasing precursor emissions, especially at northern mid-latitudes, with western North America being particularly sensitive to rising Asian emissions. We suggest that the observed increase in springtime background ozone mixing ratio may hinder the USA s compliance with its ozone air quality standard.

  11. Mixing ratio and carbon isotopic composition investigation of atmospheric CO2 in Beijing, China.

    PubMed

    Pang, Jiaping; Wen, Xuefa; Sun, Xiaomin

    2016-01-01

    The stable isotope composition of atmospheric CO2 can be used as a tracer in the study of urban carbon cycles, which are affected by anthropogenic and biogenic CO2 components. Continuous measurements of the mixing ratio and δ(13)C of atmospheric CO2 were conducted in Beijing from Nov. 15, 2012 to Mar. 8, 2014 including two heating seasons and a vegetative season. Both δ(13)C and the isotopic composition of source CO2 (δ(13)CS) were depleted in the heating seasons and enriched in the vegetative season. The diurnal variations in the CO2 mixing ratio and δ(13)C contained two peaks in the heating season, which are due to the effects of morning rush hour traffic. Seasonal and diurnal patterns of the CO2 mixing ratio and δ(13)C were affected by anthropogenic emissions and biogenic activity. Assuming that the primary CO2 sources at night (22:00-04:00) were coal and natural gas combustion during heating seasons I and II, an isotopic mass balance analysis indicated that coal combustion had average contributions of 83.83±14.11% and 86.84±12.27% and that natural gas had average contributions of 16.17±14.11% and 13.16±12.27%, respectively. The δ(13)C of background CO2 in air was the main error source in the isotopic mass balance model. Both the mixing ratio and δ(13)C of atmospheric CO2 had significant linear relationships with the air quality index (AQI) and can be used to indicate local air pollution conditions. Energy structure optimization, for example, reducing coal consumption, will improve the local air conditions in Beijing.

  12. Effects of different mixing ratios on emissions from passenger cars fueled with methanol/gasoline blends.

    PubMed

    Zhao, Hong; Ge, Yunshan; Tan, Jianwei; Yin, Hang; Guo, Jiadong; Zhao, Wei; Dai, Peipei

    2011-01-01

    Regulated and unregulated emissions from four passenger cars fueled with methanol/gasoline blends at different mixing ratios (M15, M20, M30, M50, M85 and M100) were tested over the New European Driving Cycle (NEDC). Volatile organic compounds (VOCs) were sampled by Tenax TA and analyzed by thermal desorption-gas chromatograph/mass spectrometer (TD-GC/MS). Carbonyls were trapped on dinitrophenylhydrazine (DNPH) cartridges and analyzed by high performance liquid chromatography (HPLC). The results showed that total emissions of VOCs and BTEX (benzene, toluene, ethylbenzene, p, m, o-xylene) from all vehicles fueled with methanol/gasoline blends were lower than those from vehicles fueled with only gasoline. Compared to the baseline, the use of M85 decreased BTEX emissions by 97.4%, while the use of M15 decreased it by 19.7%. At low-to-middle mixing ratios (M15, M20, M30 and M50), formaldehyde emissions showed a slight increase while those of high mixing ratios (M85 and M100) were three times compared with the baseline gasoline only. When the vehicles were retrofitted with new three-way catalytic converters (TWC), emissions of carbon monoxide (CO), total hydrocarbon (THC), and nitrogen oxides (NO(x)) were decreased by 24%-50%, 10%-35%, and 24%-58% respectively, compared with the cars using the original equipment manufacture (OEM) TWC. Using the new TWC, emissions of formaldehyde and BTEX were decreased, while those of other carbonyl increased. It is necessary that vehicles fueled with methanol/gasoline blends be retrofitted with a new TWC. In addition, the specific reactivity of emissions of vehicles fueled with M15 and retrofitted with the new TWC was reduced from 4.51 to 4.08 compared to the baseline vehicle. This indicates that the use of methanol/gasoline blend at a low mixing ratio may have lower effect on environment than gasoline.

  13. Increasing springtime ozone mixing ratios in the free troposphere over western North America.

    PubMed

    Cooper, O R; Parrish, D D; Stohl, A; Trainer, M; Nédélec, P; Thouret, V; Cammas, J P; Oltmans, S J; Johnson, B J; Tarasick, D; Leblanc, T; McDermid, I S; Jaffe, D; Gao, R; Stith, J; Ryerson, T; Aikin, K; Campos, T; Weinheimer, A; Avery, M A

    2010-01-21

    In the lowermost layer of the atmosphere-the troposphere-ozone is an important source of the hydroxyl radical, an oxidant that breaks down most pollutants and some greenhouse gases. High concentrations of tropospheric ozone are toxic, however, and have a detrimental effect on human health and ecosystem productivity. Moreover, tropospheric ozone itself acts as an effective greenhouse gas. Much of the present tropospheric ozone burden is a consequence of anthropogenic emissions of ozone precursors resulting in widespread increases in ozone concentrations since the late 1800s. At present, east Asia has the fastest-growing ozone precursor emissions. Much of the springtime east Asian pollution is exported eastwards towards western North America. Despite evidence that the exported Asian pollution produces ozone, no previous study has found a significant increase in free tropospheric ozone concentrations above the western USA since measurements began in the late 1970s. Here we compile springtime ozone measurements from many different platforms across western North America. We show a strong increase in springtime ozone mixing ratios during 1995-2008 and we have some additional evidence that a similar rate of increase in ozone mixing ratio has occurred since 1984. We find that the rate of increase in ozone mixing ratio is greatest when measurements are more heavily influenced by direct transport from Asia. Our result agrees with previous modelling studies, which indicate that global ozone concentrations should be increasing during the early part of the twenty-first century as a result of increasing precursor emissions, especially at northern mid-latitudes, with western North America being particularly sensitive to rising Asian emissions. We suggest that the observed increase in springtime background ozone mixing ratio may hinder the USA's compliance with its ozone air quality standard.

  14. Inter-comparison of 2 microm Heterodyne Differential Absorption Lidar, Laser Diode Spectrometer, LICOR NDIR analyzer and flasks measurements of near-ground atmospheric CO2 mixing ratio.

    PubMed

    Gibert, Fabien; Joly, Lilian; Xuéref-Rémy, Irène; Schmidt, Martina; Royer, Adrien; Flamant, Pierre H; Ramonet, Michel; Parvitte, Bertrand; Durry, Georges; Zéninari, Virginie

    2009-01-01

    Remote sensing and in situ instruments are presented and compared in the same location for accurate CO(2) mixing ratio measurements in the atmosphere: (1) a 2.064 microm Heterodyne DIfferential Absorption Lidar (HDIAL), (2) a field deployable infrared Laser Diode Spectrometer (LDS) using new commercial diode laser technology at 2.68 microm, (3) LICOR NDIR analyzer and (4) flasks. LDS, LICOR and flasks measurements were made in the same location, LICOR and flasks being taken as reference. Horizontal HDIAL measurements of CO(2) absorption using aerosol backscatter signal are reported. Using new spectroscopic data in the 2 microm band and meteorological sensor measurements, a mean CO(2) mixing ratio is inferred by the HDIAL in a 1 km long path above the 15m height location of the CO(2) in situ sensors. We compare HDIAL and LDS measurements with the LICOR data for 30 min of time averaging. The mean standard deviation of the HDIAL and the LDS CO(2) mixing ratio results are 3.3 ppm and 0.89 ppm, respectively. The bias of the HDIAL and the LDS measurements are -0.54 ppm and -0.99 ppm, respectively.

  15. Cloud condensation nucleus activity of secondary organic aerosol particles mixed with sulfate

    NASA Astrophysics Data System (ADS)

    King, Stephanie M.; Rosenoern, Thomas; Shilling, John E.; Chen, Qi; Martin, Scot T.

    2007-12-01

    The cloud condensation nucleus (CCN) activity of organic-sulfate particles was investigated using a steady-state environmental chamber. The organic component consisted of secondary organic aerosol (SOA) generated in the dark from 24 +/- 2 ppb α-pinene for conditions of 300 +/- 5 ppb ozone, 40 +/- 2% relative humidity, and 25 +/- 1°C, with the organic mass loading in the chamber ranging from 23 to 37 μg m-3. CCN analysis was performed for 80- to 150-nm particles having variable organic-sulfate volume fractions, which were estimated from the diameter of the organic-sulfate particle relative to that of the seed as well as independently from mass spectra. Critical supersaturation, which increased for greater SOA volume fraction and smaller particle diameter, was well predicted by a Köhler model having two components, one for ammonium sulfate and another for SOA. The entire data set could be successfully modeled by a single suite of effective chemical parameters for SOA. The results suggest that the effects of limited organic solubility in mixed SOA-sulfate particles may be reliably omitted in the treatment of cloud droplet formation.

  16. Iron Speciation and Mixing in Single Aerosol Particles from the Asian Continental Outflow

    SciTech Connect

    Moffet, Ryan C.; Furutani, Hiroshi; Rodel, Tobias; Henn, Tobias R.; Sprau, Peter; Laskin, Alexander; Uematsu, Mitsuo; Gilles, Marry K.

    2012-04-04

    Bioavailable iron from atmospheric aerosol is an essential nutrient that can control oceanic productivity, thereby impacting the global carbon budget and climate. Particles collected on Okinawa Island during an atmospheric pollution transport event from China were analyzed using complementary single particle techniques to determine the iron source and speciation. Comparing the spatial distribution of iron within ambient particles and standard Asian mineral dust, it was determined that field-collected atmospheric Fe-containing particles have numerous sources, including anthropogenic sources such as coal combustion. Fe-containing particles were found to be internally mixed with secondary species such as sulfate, soot, and organic carbon. The mass weighted average Fe(II) fraction (defined as Fe(II)/[Fe(II)+Fe(III)]) was determined to be 0.33 {+-} 0.08. Within the experimental uncertainty, this value lies close to the range of 0.26-0.30 determined for representative Asian mineral dust. Previous studies have indicated that the solubility of iron from combustion is much higher than that from mineral dust. Therefore, chemical and/or physical differences other than oxidation state may help explain the higher solubility of iron in atmospheric particles.

  17. Study of CFU for individual microorganisms in mixed cultures with a known ratio using MBRT.

    PubMed

    Nandy, Subir Kumar; Venkatesh, Kv

    2014-01-01

    Determination of metabolically active cell count is an important step in designing, operating and controlling fermentation processes. It's particularly relevant in processes involving mixed cultures, where multiple species contribute to the total growth. The motivation for the current study is to develop a methodology to estimate metabolically active cell counts for the individual species in a mixed culture with approximate equal numbers. Further, the methodology should indicate the presence of a contaminant in short time periods since in the agar plate methods used frequently it takes about 24 h. We present a methodology based on the rate of Methylene blue (MB) reduction to evaluate total count of metabolically active cells. The standard curve relating the slope of MB reduction and CFU of the individual species could be used to measure the metabolic activity of each species in the mixed culture. The slope of MB reduction could also be used to obtain the growth rate of individual species in a mixed culture and that of the total cell count. These measurements were achieved in less than 6 minutes during the growth of the cells. Evaluating the metabolic activity of individual species in a mixed culture is tedious, difficult and time consuming. The Methylene Blue dye Reduction Test (MBRT) presented here is capable of quickly estimating colony forming units (CFU) of individual species in a mixed culture if the ratio of the numbers of cells is known. The method was used to dynamically detect the occurrence of a contaminating microorganism during fermentation. The protocol developed here can be adapted to applications in processes involving mixed cultures.

  18. An enhanced VIIRS aerosol optical thickness (AOT) retrieval algorithm over land using a global surface reflectance ratio database

    NASA Astrophysics Data System (ADS)

    Zhang, Hai; Kondragunta, Shobha; Laszlo, Istvan; Liu, Hongqing; Remer, Lorraine A.; Huang, Jingfeng; Superczynski, Stephen; Ciren, Pubu

    2016-09-01

    The Visible/Infrared Imager Radiometer Suite (VIIRS) on board the Suomi National Polar-orbiting Partnership (S-NPP) satellite has been retrieving aerosol optical thickness (AOT), operationally and globally, over ocean and land since shortly after S-NPP launch in 2011. However, the current operational VIIRS AOT retrieval algorithm over land has two limitations in its assumptions for land surfaces: (1) it only retrieves AOT over the dark surfaces and (2) it assumes that the global surface reflectance ratios between VIIRS bands are constants. In this work, we develop a surface reflectance ratio database over land with a spatial resolution 0.1° × 0.1° using 2 years of VIIRS top of atmosphere reflectances. We enhance the current operational VIIRS AOT retrieval algorithm by applying the surface reflectance ratio database in the algorithm. The enhanced algorithm is able to retrieve AOT over both dark and bright surfaces. Over bright surfaces, the VIIRS AOT retrievals from the enhanced algorithm have a correlation of 0.79, mean bias of -0.008, and standard deviation (STD) of error of 0.139 when compared against the ground-based observations at the global AERONET (Aerosol Robotic Network) sites. Over dark surfaces, the VIIRS AOT retrievals using the surface reflectance ratio database improve the root-mean-square error from 0.150 to 0.123. The use of the surface reflectance ratio database also increases the data coverage of more than 20% over dark surfaces. The AOT retrievals over bright surfaces are comparable to MODIS Deep Blue AOT retrievals.

  19. Deep Uranus Cloud Structure and Methane Mixing Ratio as Constrained by Keck AO Imaging Observations.

    NASA Astrophysics Data System (ADS)

    Sromovsky, Lawrence A.; Fry, P. M.

    2006-09-01

    Keck AO imaging of Uranus in 2004 with H and H-continuum filters provide deep views of scattered light in the Uranian atmosphere with different sensitivities to methane absorption and collision-induced absorption by Hydrogen. After deconvolution, these images provide accurate low-latitude center-to-limb (east-west) profiles out to view angles of nearly 80 degrees, permitting solutions for both cloud properties and the methane mixing ratio. After accounting for a very small high-altitude haze contribution, the observed central disk I/F values for H and H-continuum filters can be modeled using an opaque semi-infinite cloud of very low albedo (near 0.04), a broken cloud of high albedo (fractional coverage near 0.04-.06), or a continuous cloud of low optical depth (0.2-1.0) containing particles of high single-scattering albedo. For low methane mixing ratios (0.5-1 percent) the central disk I/F values require a deep cloud (near 8 bars), while for the high methane mixing ratios (2-4 percent) a higher altitude solution is possible (near 3 bars). However, the observed slightly limb-brightened and relatively flat center-to-limb H-continuum profile is only consistent with an optically thin cloud. The best-fit solution is a low methane mixing ratio (0.75-1.0 percent vmr), and a deep low opacity cloud (optical depth ranging from 0.2 to 0.4 for scattering asymmetry parameters ranging from 0 to 0.3). This CH4 mixing ratio is slightly below the lower limit of the Baines et al. (1995, Icarus 114, 328-340) result of 1.6(+0.7/-0.5) percent. This work was supported by NASA's Planetary Astronomy and Planetary Atmospheres programs and the W.M. Keck Observatory. We thank those of Hawaiian ancestry whose generous hospitality in allowing use of their sacred mountain made the observations possible.

  20. Size distribution, mixing state and source apportionment of black carbon aerosol in London during wintertime

    NASA Astrophysics Data System (ADS)

    Liu, D.; Allan, J. D.; Young, D. E.; Coe, H.; Beddows, D.; Fleming, Z. L.; Flynn, M. J.; Gallagher, M. W.; Harrison, R. M.; Lee, J.; Prevot, A. S. H.; Taylor, J. W.; Yin, J.; Williams, P. I.; Zotter, P.

    2014-09-01

    Black carbon aerosols (BC) at a London urban site were characterised in both winter- and summertime 2012 during the Clean Air for London (ClearfLo) project. Positive matrix factorisation (PMF) factors of organic aerosol mass spectra measured by a high-resolution aerosol mass spectrometer (HR-AMS) showed traffic-dominant sources in summer but in winter the influence of additional non-traffic sources became more important, mainly from solid fuel sources (SF). Measurements using a single particle soot photometer (SP2, DMT), showed the traffic-dominant BC exhibited an almost uniform BC core size (Dc) distribution with very thin coating thickness throughout the detectable range of Dc. However, the size distribution of sf (project average mass median Dc = 149 ± 22 nm in winter, and 120 ± 6 nm in summer) and BC coating thickness varied significantly in winter. A novel methodology was developed to attribute the BC number concentrations and mass abundances from traffic (BCtr) and from SF (BCsf), by using a 2-D histogram of the particle optical properties as a function of BC core size, as measured by the SP2. The BCtr and BCsf showed distinctly different sf distributions and coating thicknesses, with BCsf displaying larger Dc and larger coating thickness compared to BCtr. BC particles from different sources were also apportioned by applying a multiple linear regression between the total BC mass and each AMS-PMF factor (BC-AMS-PMF method), and also attributed by applying the absorption spectral dependence of carbonaceous aerosols to 7-wavelength Aethalometer measurements (Aethalometer method). Air masses that originated from westerly (W), southeasterly (SE), and easterly (E) sectors showed BCsf fractions that ranged from low to high, and whose mass median Dc values were 137 ± 10 nm, 143 ± 11 nm and 169 ± 29 nm, respectively. The corresponding bulk relative coating thickness of BC (coated particle size/BC core - Dp/Dc) for these same sectors was 1.28 ± 0.07, 1.45 ± 0

  1. Size distribution, mixing state and source apportionments of black carbon aerosols in London during winter time

    NASA Astrophysics Data System (ADS)

    Liu, D.; Allan, J. D.; Young, D. E.; Coe, H.; Beddows, D.; Fleming, Z. L.; Flynn, M. J.; Gallagher, M. W.; Harrison, R. M.; Lee, J.; Prevot, A. S. H.; Taylor, J. W.; Yin, J.; Williams, P. I.; Zotter, P.

    2014-06-01

    Black carbon aerosols (BC) at a London urban site were characterized in both winter and summer time 2012 during the Clean Air for London (ClearfLo) project. Positive matrix factorization (PMF) factors of organic aerosol mass spectra measured by a high resolution aerosol mass spectrometer (HR-AMS) showed traffic-dominant sources in summer but in winter the influence of additional non-traffic sources became more important, mainly from solid fuel sources (SF). Measurements using a single particle soot photometer (SP2, DMT), showed the traffic-dominant BC exhibited an almost uniform BC core size (Dc) distribution with very thin coating thickness throughout the detectable range of Dc. However the size distribution of Dc (project average mass median Dc = 149 ± 22 nm in winter, and 120 ± 6 nm in summer) and BC coating thickness varied significantly in winter. A novel methodology was developed to attribute the BC number concentrations and mass abundances from traffic (BCtr) and from SF (BCsf), by using a 2-D histogram of the particle optical properties as a function of BC core size, as measured by the SP2. The BCtr and BCsf showed distinctly different Dc distributions and coating thicknesses, with BCsf displaying larger Dc and larger coating thickness compared to BCtr. BC particles from different sources were also apportioned by applying a multiple linear regression between the total BC mass and each AMS-PMF factor (BC-AMS-PMF method), and also attributed by applying the absorption spectral dependence of carbonaceous aerosols to 7-wavelength Aethalometer measurements (Aethalometer method). Air masses that originated from westerly (W), southeasterly (SE), or easterly (E) sectors showed BCsf fractions that ranged from low to high, and whose mass median Dc values were 137 ± 10 nm, 143 ± 11 nm, and 169 ± 29 nm respectively. The corresponding bulk relative coating thickness of BC (coated particle size / BC core - Dp / Dc) for these same sectors was 1.28 ± 0.07, 1.45 ± 0

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

    NASA Astrophysics Data System (ADS)

    Jacobson, M. Z.

    2005-12-01

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

  3. Evaluation of Aerosol Mixing State Classes in the GISS Modele-matrix Climate Model Using Single-particle Mass Spectrometry Measurements

    NASA Technical Reports Server (NTRS)

    Bauer, Susanne E.; Ault, Andrew; Prather, Kimberly A.

    2013-01-01

    Aerosol particles in the atmosphere are composed of multiple chemical species. The aerosol mixing state, which describes how chemical species are mixed at the single-particle level, provides critical information on microphysical characteristics that determine the interaction of aerosols with the climate system. The evaluation of mixing state has become the next challenge. This study uses aerosol time-of-flight mass spectrometry (ATOFMS) data and compares the results to those of the Goddard Institute for Space Studies modelE-MATRIX (Multiconfiguration Aerosol TRacker of mIXing state) model, a global climate model that includes a detailed aerosol microphysical scheme. We use data from field campaigns that examine a variety of air mass regimens (urban, rural, and maritime). At all locations, polluted areas in California (Riverside, La Jolla, and Long Beach), a remote location in the Sierra Nevada Mountains (Sugar Pine) and observations from Jeju (South Korea), the majority of aerosol species are internally mixed. Coarse aerosol particles, those above 1 micron, are typically aged, such as coated dust or reacted sea-salt particles. Particles below 1 micron contain large fractions of organic material, internally-mixed with sulfate and black carbon, and few external mixtures. We conclude that observations taken over multiple weeks characterize typical air mass types at a given location well; however, due to the instrumentation, we could not evaluate mass budgets. These results represent the first detailed comparison of single-particle mixing states in a global climate model with real-time single-particle mass spectrometry data, an important step in improving the representation of mixing state in global climate models.

  4. Evaluation of aerosol mixing state classes in the GISS modelE-MATRIX climate model using single-particle mass spectrometry measurements

    NASA Astrophysics Data System (ADS)

    Bauer, Susanne E.; Ault, Andrew; Prather, Kimberly A.

    2013-09-01

    Aerosol particles in the atmosphere are composed of multiple chemical species. The aerosol mixing state, which describes how chemical species are mixed at the single-particle level, provides critical information on microphysical characteristics that determine the interaction of aerosols with the climate system. The evaluation of mixing state has become the next challenge. This study uses aerosol time-of-flight mass spectrometry (ATOFMS) data and compares the results to those of the Goddard Institute for Space Studies modelE-MATRIX (Multiconfiguration Aerosol TRacker of mIXing state) model, a global climate model that includes a detailed aerosol microphysical scheme. We use data from field campaigns that examine a variety of air mass regimens (urban, rural, and maritime). At all locations, polluted areas in California (Riverside, La Jolla, and Long Beach), a remote location in the Sierra Nevada Mountains (Sugar Pine) and observations from Jeju (South Korea), the majority of aerosol species are internally mixed. Coarse aerosol particles, those above 1 µm, are typically aged, such as coated dust or reacted sea-salt particles. Particles below 1 µm contain large fractions of organic material, internally mixed with sulfate and black carbon, and few external mixtures. We conclude that observations taken over multiple weeks characterize typical air mass types at a given location well; however, due to the instrumentation, we could not evaluate mass budgets. These results represent the first detailed comparison of single-particle mixing states in a global climate model with real-time single-particle mass spectrometry data, an important step in improving the representation of mixing state in global climate models.

  5. Finite mixture models for the computation of isotope ratios in mixed isotopic samples

    NASA Astrophysics Data System (ADS)

    Koffler, Daniel; Laaha, Gregor; Leisch, Friedrich; Kappel, Stefanie; Prohaska, Thomas

    2013-04-01

    Finite mixture models have been used for more than 100 years, but have seen a real boost in popularity over the last two decades due to the tremendous increase in available computing power. The areas of application of mixture models range from biology and medicine to physics, economics and marketing. These models can be applied to data where observations originate from various groups and where group affiliations are not known, as is the case for multiple isotope ratios present in mixed isotopic samples. Recently, the potential of finite mixture models for the computation of 235U/238U isotope ratios from transient signals measured in individual (sub-)µm-sized particles by laser ablation - multi-collector - inductively coupled plasma mass spectrometry (LA-MC-ICPMS) was demonstrated by Kappel et al. [1]. The particles, which were deposited on the same substrate, were certified with respect to their isotopic compositions. Here, we focus on the statistical model and its application to isotope data in ecogeochemistry. Commonly applied evaluation approaches for mixed isotopic samples are time-consuming and are dependent on the judgement of the analyst. Thus, isotopic compositions may be overlooked due to the presence of more dominant constituents. Evaluation using finite mixture models can be accomplished unsupervised and automatically. The models try to fit several linear models (regression lines) to subgroups of data taking the respective slope as estimation for the isotope ratio. The finite mixture models are parameterised by: • The number of different ratios. • Number of points belonging to each ratio-group. • The ratios (i.e. slopes) of each group. Fitting of the parameters is done by maximising the log-likelihood function using an iterative expectation-maximisation (EM) algorithm. In each iteration step, groups of size smaller than a control parameter are dropped; thereby the number of different ratios is determined. The analyst only influences some control

  6. European isotopic signatures for lead in atmospheric aerosols: a source apportionment based upon 206Pb/207Pb ratios.

    PubMed

    Flament, Pascal; Bertho, Marie-Laure; Deboudt, Karine; Véron, Alain; Puskaric, Emile

    2002-09-16

    To investigate the capability of the lead isotope signature technique to support a source apportionment study at a Continental scale, atmospheric particulate matter was collected at Cap Gris-Nez (Eastern Channel, northern France), over one year (1995-1996). Four days retrospective trajectories of air masses were available during each sampling experiment. Twenty-eight samples, for which the origin of aerosols was unambiguously determined, were selected for isotopic measurements. Considering the Enrichment Factors, EF(Crust) of lead and its size distribution, we show that lead is mostly from anthropogenic origin and mainly associated with [0.4 < diameter < 0.9 microm] particles. The extent to which various Continental sources influence the lead abundance in aerosols is exhibited by considering both the lead concentration and the origin of air masses. Lead concentration is higher by a factor of approximately seven, when air masses are derived from Continental Europe, by comparison with marine air masses. Taking into account these concentrations and the vertical movements of air masses, we compare the different isotopic compositions using a statistical non-parametric test (Kolmogorov-Smirnov). We produce evidence that, for most of the cases, air masses originating from Continental Europe exhibit a more radiogenic composition (1.134 < 206Pb/207Pb < 1.172) than air masses coming from the United Kingdom (1.106 < 206Pb/207Pb < 1.124). Generally, lead isotopic compositions in aerosols are clearly distinct from the gasoline signatures in European countries, strongly suggesting that automotive lead is no longer the major component of this metal in the air. Gasoline and industrial isotopic signatures could explain the origin of lead in our aerosol samples. A source apportionment based upon 206Pb/207Pb ratios, suggests that the difference between British (206Pb/207Pb = 1.122 +/- 0.038) and Continental (206Pb/207Pb = 1.155 +/- 0.022) signatures may be largely explained by

  7. Modelling the chemically aged and mixed aerosols over the eastern central Atlantic Ocean - potential impacts

    NASA Astrophysics Data System (ADS)

    Astitha, M.; Kallos, G.; Spyrou, C.; O'Hirok, W.; Lelieveld, J.; Denier van der Gon, H. A. C.

    2010-07-01

    Detailed information on the chemical and physical properties of aerosols is important for assessing their role in air quality and climate. This work explores the origin and fate of continental aerosols transported over the Central Atlantic Ocean, in terms of chemical composition, number and size distribution, using chemistry-transport models, satellite data and in situ measurements. We focus on August 2005, a period with intense hurricane and tropical storm activity over the Atlantic Ocean. A mixture of anthropogenic (sulphates, nitrates), natural (desert dust, sea salt) and chemically aged (sulphate and nitrate on dust) aerosols is found entering the hurricane genesis region, most likely interacting with clouds in the area. Results from our modelling study suggest rather small amounts of accumulation mode desert dust, sea salt and chemically aged dust aerosols in this Atlantic Ocean region. Aerosols of smaller size (Aitken mode) are more abundant in the area and in some occasions sulphates of anthropogenic origin and desert dust are of the same magnitude in terms of number concentrations. Typical aerosol number concentrations are derived for the vertical layers near shallow cloud formation regimes, indicating that the aerosol number concentration can reach several thousand particles per cubic centimetre. The vertical distribution of the aerosols shows that the desert dust particles are often transported near the top of the marine cloud layer as they enter into the region where deep convection is initiated. The anthropogenic sulphate aerosol can be transported within a thick layer and enter the cloud deck through multiple ways (from the top, the base of the cloud, and by entrainment). The sodium (sea salt related) aerosol is mostly found below the cloud base. The results of this work may provide insights relevant for studies that consider aerosol influences on cloud processes and storm development in the Central Atlantic region.

  8. Chemically aged and mixed aerosols over the Central Atlantic Ocean - potential impacts

    NASA Astrophysics Data System (ADS)

    Astitha, M.; Kallos, G.; Spyrou, C.; O'Hirok, W.; Lelieveld, J.; Denier van der Gon, H. A. C.

    2010-02-01

    Detailed information on the chemical and physical properties of aerosols is important for assessing their role in air quality and climate. This work explores the origin and fate of continental aerosols transported over the Central Atlantic Ocean, in terms of chemical composition, number and size distribution, using chemistry-transport models, satellite data and in situ measurements. We focus on August 2005, a period with intense hurricane and tropical storm activity over the Atlantic Ocean. A mixture of anthropogenic (sulphates, nitrates), natural (desert dust, sea salt) and chemically aged (sulphate and nitrate on dust) aerosols is found entering the hurricane genesis region, most likely interacting with clouds in the area. Results from our modelling study suggest rather small amounts of accumulation mode desert dust, sea salt and chemically aged dust aerosols in this Atlantic Ocean region. Aerosols of smaller size (Aitken mode) are more abundant in the area and in some occasions sulphates of anthropogenic origin and desert dust are of the same magnitude in terms of number concentrations. Typical aerosol number concentrations are derived for the vertical layers near shallow cloud formation regimes, designating that the aerosol number concentration can reach several thousand particles per cubic centimetre. The vertical distribution of the aerosols indicates that the desert dust particles are often transported near the top of the marine cloud layer as they enter into the region where deep convection is initiated. The anthropogenic sulphate aerosol can be transported within a thick layer and enter the cloud deck through multiple ways (from the top, the base of the cloud and entrainment). The sodium (sea salt related) aerosol is mostly found below the cloud base. The results of this work may provide insights relevant for studies that consider aerosol influences on cloud processes and storm development in the Central Atlantic region.

  9. The role of grain-size ratio in the mobility of mixed granular beds

    NASA Astrophysics Data System (ADS)

    Staudt, Franziska; Mullarney, Julia C.; Pilditch, Conrad A.; Huhn, Katrin

    2017-02-01

    The main goal of the study was to understand the effects of grain-size distribution on the stability of beds in the sand-silt range, which is a critical subject for the understanding of geomorphological processes in aquatic environments. Although theoretical models can explain the mobilization of a mixed bed, there is a clear lack in knowledge regarding the stabilizing effect of non-cohesive fine material. To connect existing findings, we analysed bed stability in relation to grain-size distribution in laboratory experiments. Erosion experiments in an annular flume were conducted using beds of different size compositions of spherical glass beads, i.e. a) the grain-size ratio RD = D50,coarse/D50,fine (the relative size of coarse and fine grains; D50 = 39-367 μm) and b) the amount of fines. Several glass-bead combinations with unimodal and bimodal grain-size distributions (RD = 3.9, 5.8, and 9.4) and varying fine fractions (10-40% dry weight) were subjected to increasing flow speeds (0.01-0.19 m s-1). Using acoustic Doppler velocimetry (ADV) and optical backscatter, the flow profile in the vicinity of the bed surface, the changes in bed morphology, and the suspended sediment concentration (SSC) were measured. A new method was developed to evaluate the bed-level changes detected by the ADV as a proxy for the bed mobility. We found different modes of bed mobility depending on the grain-size ratio. For low grain-size ratios, an increase in the fine fraction (to 40%) led to increased bed-level changes during the experiment and the mobilization of the mixed bed at the highest flow speed. For high ratios an increase in fine fraction (to 40%) led to a decrease of bed-level changes and the beds remained stable, i.e. no bed forms developed even at the highest flow speed. Therefore, increasing the amount of fine particles can lead to different modes of behaviour depending on the grain-size ratio. For a bimodal sediment bed with spherical grains under unidirectional flow

  10. Optical Properties of Mixed Black Carbon, Inorganic and Secondary Organic Aerosols

    SciTech Connect

    Paulson, S E

    2012-05-30

    Summarizes the achievements of the project, which are divided into four areas: 1) Optical properties of secondary organic aerosols; 2) Development and of a polar nephelometer to measure aerosol optical properties and theoretical approaches to several optical analysis problems, 3) Studies on the accuracy of measurements of absorbing carbon by several methods, and 4) Environmental impacts of biodiesel.

  11. Mixing Characteristics of Coaxial Injectors at High Gas to Liquid Momentum Ratios

    NASA Technical Reports Server (NTRS)

    Strakey, P. A.; Talley, D. G.; Hutt, J. J.

    1999-01-01

    A study of the spray of a swirl coaxial gas-liquid injector operating at high gas to liquid momentum ratios is reported. Mixing and droplet size characteristics of the swirl injector are also compared to a shear coaxial injector, currently being used in the Space Shuttle Main Engine fuel preburner. The injectors were tested at elevated chamber pressures using water as a LOX simulant and nitrogen and helium as gaseous hydrogen simulants. The elevated chamber pressure allowed for matching of several of the preburner injector conditions including; gas to liquid momentum ratio, density ratio and Mach number. Diagnostic techniques used to characterize the spray included; strobe back-light imaging, laser sheet spray imaging, mechanical patternation, and a phase Doppler interferometry. Results thus far indicate that the radial spreading of the swirl coaxial spray is much less than was reported in previous studies of swirl injectors operating at atmospheric back-pressure. The swirl coaxial spray does, however, exhibit a smaller overall droplet size which may be interpreted as an increase in local mixing.

  12. Direct isotope ratio analysis of individual uranium-plutonium mixed particles with various U/Pu ratios by thermal ionization mass spectrometry.

    PubMed

    Suzuki, Daisuke; Esaka, Fumitaka; Miyamoto, Yutaka; Magara, Masaaki

    2015-02-01

    Uranium and plutonium isotope ratios in individual uranium-plutonium (U-Pu) mixed particles with various U/Pu atomic ratios were analyzed without prior chemical separation by thermal ionization mass spectrometry (TIMS). Prior to measurement, micron-sized particles with U/Pu ratios of 1, 5, 10, 18, and 70 were produced from uranium and plutonium certified reference materials. In the TIMS analysis, the peaks of americium, plutonium, and uranium ion signals were successfully separated by continuously increasing the evaporation filament current. Consequently, the uranium and plutonium isotope ratios, except the (238)Pu/(239)Pu ratio, were successfully determined for the particles at all U/Pu ratios. This indicates that TIMS direct analysis allows for the measurement of individual U-Pu mixed particles without prior chemical separation.

  13. Asymptotic solution of the turbulent mixing layer for velocity ratio close to unity

    NASA Technical Reports Server (NTRS)

    Higuera, F. J.; Jimenez, J.; Linan, A.

    1996-01-01

    The equations describing the first two terms of an asymptotic expansion of the solution of the planar turbulent mixing layer for values of the velocity ratio close to one are obtained. The first term of this expansion is the solution of the well-known time-evolving problem and the second, which includes the effects of the increase of the turbulence scales in the stream-wise direction, obeys a linear system of equations. Numerical solutions of these equations for a two-dimensional reacting mixing layer show that the correction to the time-evolving solution may explain the asymmetry of the entrainment and the differences in product generation observed in flip experiments.

  14. Computation of Phase Equilibria, State Diagrams and Gas/Particle Partitioning of Mixed Organic-Inorganic Aerosols

    NASA Astrophysics Data System (ADS)

    Zuend, A.; Marcolli, C.; Peter, T.

    2009-04-01

    The chemical composition of organic-inorganic aerosols is linked to several processes and specific topics in the field of atmospheric aerosol science. Photochemical oxidation of organics in the gas phase lowers the volatility of semi-volatile compounds and contributes to the particulate matter by gas/particle partitioning. Heterogeneous chemistry and changes in the ambient relative humidity influence the aerosol composition as well. Molecular interactions between condensed phase species show typically non-ideal thermodynamic behavior. Liquid-liquid phase separations into a mainly polar, aqueous and a less polar, organic phase may considerably influence the gas/particle partitioning of semi-volatile organics and inorganics (Erdakos and Pankow, 2004; Chang and Pankow, 2006). Moreover, the phases present in the aerosol particles feed back on the heterogeneous, multi-phase chemistry, influence the scattering and absorption of radiation and affect the CCN ability of the particles. Non-ideal thermodynamic behavior in mixtures is usually described by an expression for the excess Gibbs energy, enabling the calculation of activity coefficients. We use the group-contribution model AIOMFAC (Zuend et al., 2008) to calculate activity coefficients, chemical potentials and the total Gibbs energy of mixed organic-inorganic systems. This thermodynamic model was combined with a robust global optimization module to compute potential liquid-liquid (LLE) and vapor-liquid-liquid equilibria (VLLE) as a function of particle composition at room temperature. And related to that, the gas/particle partitioning of semi-volatile components. Furthermore, we compute the thermodynamic stability (spinodal limits) of single-phase solutions, which provides information on the process type and kinetics of a phase separation. References Chang, E. I. and Pankow, J. F.: Prediction of activity coefficients in liquid aerosol particles containing organic compounds, dissolved inorganic salts, and water - Part

  15. Hygroscopicity of organic compounds from biomass burning and their influence on the water uptake of mixed organic ammonium sulfate aerosols

    NASA Astrophysics Data System (ADS)

    Lei, T.; Zuend, A.; Wang, W. G.; Zhang, Y. H.; Ge, M. F.

    2014-10-01

    Hygroscopic behavior of organic compounds, including levoglucosan, 4-hydroxybenzoic acid, and humic acid, as well as their effects on the hygroscopic properties of ammonium sulfate (AS) in internally mixed particles are studied by a hygroscopicity tandem differential mobility analyzer (HTDMA). The organic compounds used represent pyrolysis products of wood that are emitted from biomass burning sources. It is found that humic acid aerosol particles only slightly take up water, starting at RH (relative humidity) above ~70%. This is contrasted by the continuous water absorption of levoglucosan aerosol particles in the range 5-90% RH. However, no hygroscopic growth is observed for 4-hydroxybenzoic acid aerosol particles. Predicted water uptake using the ideal solution theory, the AIOMFAC model and the E-AIM (with UNIFAC) model are consistent with measured hygroscopic growth factors of levoglucosan. However, the use of these models without consideration of crystalline organic phases is not appropriate to describe the hygroscopicity of organics that do not exhibit continuous water uptake, such as 4-hydroxybenzoic acid and humic acid. Mixed aerosol particles consisting of ammonium sulfate and levoglucosan, 4-hydroxybenzoic acid, or humic acid with different organic mass fractions, take up a reduced amount of water above 80% RH (above AS deliquescence) relative to pure ammonium sulfate aerosol particles of the same mass. Hygroscopic growth of mixtures of ammonium sulfate and levoglucosan with different organic mass fractions agree well with the predictions of the thermodynamic models. Use of the Zdanovskii-Stokes-Robinson (ZSR) relation and AIOMFAC model lead to good agreement with measured growth factors of mixtures of ammonium sulfate with 4-hydroxybenzoic acid assuming an insoluble organic phase. Deviations of model predictions from the HTDMA measurement are mainly due to the occurrence of a microscopical solid phase restructuring at increased humidity (morphology

  16. Mixing ratios of trace gases in the austral polar atmosphere during August and September of 1987

    NASA Technical Reports Server (NTRS)

    Vedder, James F.; Heidt, Leroy E.; Pollock, Walter H.; Henry, Bruce E.; Lueb, Richard A.

    1988-01-01

    Mixing ratios are presented for a number of long-lived trace gases in the austral polar atmosphere during August and September of 1987. The recent discovery of a 12-year trend of increasing depletion of ozone over the Antarctic Continent in the spring of each year led to numerous theoretical interpretations and several scientific expeditions to the region. The results herein were obtained as part of a major effort involving penetration of the region of ozone depletion by NASA's multi-instrumented aircraft. One of the 14 instruments on the high-altitude ER-2 aircraft collected pressurized air samples between latitudes of 53 degrees and 72 degrees south at pressure altitudes up to 21 km in a series of 12 flights from Punta Arenas, Chile, over the Palmer Peninsula. The sampling system, located in the nose section of ER-2, has an inlet tube in the free airstream, a metal-bellows air pump, and 14 specially treated 1.6 l stainless-steel canisters for containing the pressurized air at 350 kPa. A typical flight profile consisted of a southbound path on the 428 K potential temperature surface, a descent to a pressure altitude of 13.7 km, a climb to the 460 K surface, and return on this surface. Mixing ratios for the trace gases were obtained from gas chromatographic analyses of the pressurized air samples. Of the species measured, the mixing ratios for CH4, CO, N2O, CF2 Cl2, CFCl3, CH3, CCl3, CCl4, and C2F3Cl3 are reported here.

  17. Boundary Layer CO2 mixing ratio measurements by an airborne pulsed IPDA lidar

    NASA Astrophysics Data System (ADS)

    Ramanathan, A. K.; Mao, J.; Abshire, J. B.; Allan, G. R.

    2014-12-01

    Since the primary signature of CO2 fluxes at the surface occurs in the planetary boundary layer (PBL), remote sensing measurements of CO2 that can resolve the CO2 absorption in the PBL separate from the total column are more sensitive to fluxes than those that can only measure a total column. The NASA Goddard CO2 sounder is a pulsed, range-resolved lidar that samples multiple (presently 30) wavelengths across the 1572.335 nm CO2 absorption line. The range resolution and line shape measurement enable CO2 mixing ratio measurements to be made in two or more altitude layers including the PBL via lidar cloud-slicing and multi-layer retrievals techniques. The pulsed lidar approach allows range-resolved backscatter of scattering from ground and cloud tops. Post flight data analysis can be used split the vertical CO2 column into layers (lidar cloud-slicing) and solve for the CO2 mixing ratio in each layer. We have demonstrated lidar cloud slicing with lidar measurements from a flight over Iowa, USA in August 2011 during the corn-growing season, remotely measuring a ≈15 ppm drawdown in the PBL CO2. We will present results using an improved lidar cloud slicing retrieval algorithm as well as preliminary measurements from the upcoming ASCENDS 2014 flight campaign. The CO2 absorption line is also more pressure broadened at lower altitudes. Analyzing the line shape also allows solving for some vertical resolution in the CO2 distribution. By allowing the retrieval process to independently vary the column concentrations in two or more altitude layers, one can perform a best-fit retrieval to obtain the CO2 mixing ratios in each of the layers. Analysis of airborne lidar measurements (in 2011) over Iowa, USA and Four Corners, New Mexico, USA show that for altitudes above 8 km, the CO2 sounder can detect and measure enhanced or diminished CO2 mixing ratios in the PBL even in the absence of clouds. We will present these results as well as preliminary measurements from the upcoming

  18. Investigations of boundary layer structure, cloud characteristics and vertical mixing of aerosols at Barbados with large eddy simulations

    NASA Astrophysics Data System (ADS)

    Jähn, Michael; Muñoz-Esparza, Domingo; Chouza, Fernando; Reitebuch, Oliver; Knoth, Oswald; Haarig, Moritz; Ansmann, Albert; Tegen, Ina

    2016-04-01

    Large eddy simulations (LESs) with ASAM (All Scale Atmospheric Model) are performed for the area of the Caribbean island Barbados to investigate island effects on boundary layer modification, cloud generation and vertical mixing of aerosols. In order to generate inflow turbulence consistent with the upstream marine boundary layer forcing, we use the cell perturbation method based on finite amplitude potential temperature perturbations. This method is now also validated for moist boundary layer simulations with open lateral boundary conditions. Observational data obtained from the SALTRACE (Saharan Aerosol Long-range Transport and Aerosol-Cloud-Interaction Experiment) field campaign is used for both model initialization and comparisons. Several sensitivity tests are carried out to demonstrate the problems related to "gray zone modeling" or when the turbulent marine boundary layer flow is replaced by laminar winds. Additional simulation cases deal with modified surface characteristics and their impacts on the simulation results. Saharan dust layers that reach Barbados via long-range transport over the North Atlantic are included as passive tracers in the model. Effects of layer thinning, subsidence and turbulent downward transport near the layer bottom at z ≈ 1800 m become apparent. The exact position of these layers and strength of downward mixing is found to be mainly controlled atmospheric stability (especially inversion strength) and wind shear. Comparisons of LES model output with lidar data show similarities in the downwind vertical wind structure and accurately reproduces the development of the daytime convective boundary layer measured by the Raman lidar.

  19. Parametric experimental studies on mixing characteristics within a low area ratio rectangular supersonic gaseous ejector

    NASA Astrophysics Data System (ADS)

    Karthick, S. K.; Rao, Srisha M. V.; Jagadeesh, G.; Reddy, K. P. J.

    2016-07-01

    We use the rectangular gaseous supersonic ejector as a platform to study the mixing characteristics of a confined supersonic jet. The entrainment ratio (ER) of the ejector, the non-mixed length (LNM), and potential core length (LPC) of the primary supersonic jet are measures to characterize mixing within the supersonic ejector. Experiments are carried out on a low area ratio rectangular supersonic ejector with air as the working fluid in both primary and secondary flows. The design Mach number of the nozzle (MPD = 1.5-3.0) and primary flow stagnation pressure (Pop = 4.89-9.89 bars) are the parameters that are varied during experimentation. Wall static pressure measurements are carried out to understand the performance of the ejector as well as to estimate the LNM (the spatial resolution is limited by the placement of pressure transducers). Well-resolved flow images (with a spatial resolution of 50 μm/pixel and temporal resolution of 1.25 ms) obtained through Planar Laser Mie Scattering (PLMS) show the flow dynamics within the ejector with clarity. The primary flow and secondary flow are seeded separately with acetone that makes the LNM and LPC clearly visible in the flow images. These parameters are extracted from the flow images using in-house image processing routines. A significant development in this work is the definition of new scaling parameters within the ejector. LNM, non-dimensionalized with respect to the fully expanded jet height hJ, is found to be a linear function of the Mach number ratio (Mach number ratio is defined as the ratio of design Mach number (MPD) and fully expanded Mach number (MPJ) of the primary jet). This definition also provides a clear demarcation of under-expanded and over-expanded regimes of operation according to [MPD/MPJ] > 1 and [MPD/MPJ] < 1, respectively. It is observed that the ER increased in over-expanded mode (to 120%) and decreased in under-expanded mode (to 68%). Similarly, LNM decreased (to 21.8%) in over-expanded mode

  20. Regional and hemispheric influences on measured spring peroxyacetyl nitrate (PAN) mixing ratios at the Auchencorth UK EMEP supersite

    NASA Astrophysics Data System (ADS)

    Malley, Christopher S.; Cape, J. Neil; Jones, Matthew R.; Leeson, Sarah R.; Coyle, Mhairi; Braban, Christine F.; Heal, Mathew R.; Twigg, Marsailidh M.

    2016-06-01

    This work presents 15-min averaged measurements of peroxyacetyl nitrate (PAN) obtained during spring 2014 (24/04/2014 - 06/05/2014) at the Auchencorth UK EMEP supersite (southeast Scotland). The aim of this analysis was to investigate the conditions producing the distribution of PAN mixing ratios at the supersite in spring 2014. Air mass back trajectories showed the majority of air masses to have spent substantial time over the UK, continental Europe or Scandinavia prior to arrival at Auchencorth. The median and 95th percentile PAN mixing ratios observed were 0.46 ppb and 1.03 ppb, respectively. The median mixing ratio was elevated compared with previous PAN measurements during springtime (April-May) in southeast Scotland (corresponding median mixing ratios April-May 1994-1998: 0.1-0.3 ppb), which is hypothesised to be due to conditions conducive to regional (European) photochemical PAN production. Additionally, PAN mixing ratios during regionally influenced conditions (0.4-1.5 ppb) were substantially more elevated from hemispheric background mixing ratios (0.4-0.6 ppb) than for ozone (O3, regional: 10-45 ppb, hemispheric: 30-40 ppb). PAN and O3 both impact upon vegetation and human health and it is necessary to understand the extent to which hemispheric and regional processes contribute to their abundances in different locations. Regional processes can both increase and decrease PAN and O3 mixing ratios compared to imported hemispheric background mixing ratios. This study concludes that during the measurement period in spring 2014 at the Auchencorth supersite, regional PAN and O3 modifying processes enhanced PAN mixing ratios more than for O3.

  1. Lidar Ratios for Dust Aerosols Derived From Retrievals of CALIPSO Visible Extinction Profiles Constrained by Optical Depths from MODIS-Aqua and CALIPSO/CloudSat Ocean Surface Reflectance Measurements

    NASA Technical Reports Server (NTRS)

    Young, Stuart A.; Josset, Damien B.; Vaughan, Mark A.

    2010-01-01

    CALIPSO's (Cloud Aerosol Lidar Infrared Pathfinder Satellite Observations) analysis algorithms generally require the use of tabulated values of the lidar ratio in order to retrieve aerosol extinction and optical depth from measured profiles of attenuated backscatter. However, for any given time or location, the lidar ratio for a given aerosol type can differ from the tabulated value. To gain some insight as to the extent of the variability, we here calculate the lidar ratio for dust aerosols using aerosol optical depth constraints from two sources. Daytime measurements are constrained using Level 2, Collection 5, 550-nm aerosol optical depth measurements made over the ocean by the MODIS (Moderate Resolution Imaging Spectroradiometer) on board the Aqua satellite, which flies in formation with CALIPSO. We also retrieve lidar ratios from night-time profiles constrained by aerosol column optical depths obtained by analysis of CALIPSO and CloudSat backscatter signals from the ocean surface.

  2. Applications of High-Resolution Electrospray Ionization Mass Spectrometry to Measurements of Average Oxygen to Carbon Ratios in Secondary Organic Aerosols

    SciTech Connect

    Bateman, Adam P.; Laskin, Julia; Laskin, Alexander; Nizkorodov, Sergey

    2012-07-02

    The applicability of high resolution electrospray ionization mass spectrometry (HR ESI-MS) to measurements of the average oxygen to carbon ratio (O/C) in organic aerosols was investigated. Solutions with known average O/C containing up to 10 standard compounds representative of secondary organic aerosol (SOA) were analyzed and corresponding electrospray ionization efficiencies were quantified. The assumption of equal ionization efficiency commonly used in estimating O/C ratios of organic aerosols was found to be reasonably accurate. We found that the accuracy of the measured O/C ratios increases by averaging the values obtained from both (+) and (-) modes. A correlation was found between the ratio of the ionization efficiencies in the positive and negative ESI modes with the octanol-water partition constant, and more importantly, with the compound's O/C. To demonstrate the utility of this correlation for estimating average O/C values of unknown mixtures, we analyzed the ESI (+) and ESI (-) data for SOA produced by oxidation of limonene and isoprene and compared to online O/C measurements using an aerosol mass spectrometer (AMS). This work demonstrates that the accuracy of the HR ESI-MS methods is comparable to that of the AMS, with the added benefit of molecular identification of the aerosol constituents.

  3. The global methane cycle: isotopes and mixing ratios, sources and sinks.

    PubMed

    Bréas, O; Guillou, C; Reniero, F; Wada, E

    2001-01-01

    A review of the global cycle of methane is presented with emphasis on its isotopic composition. The history of methane mixing ratios, reconstructed from measurements of air trapped in ice-cores is described. The methane record now extends back to 420 kyr ago in the case of the Vostok ice cores from Antarctica. The trends in mixing ratios and in delta13C values are reported for the two Hemispheres. The increase of the atmospheric methane concentration over the past 200 years, and by 1% per year since 1978, reaching 1.7 ppmv in 1990 is underlined. The various methane sources are presented. Indeed the authors describe the methane emissions by bacterial activity under anaerobic conditions in wet environments (wetlands, bogs, tundra, rice paddies), in ruminant stomachs and termite guts, and that originating from fossil carbon sources, such as biomass burning, coal mining, industrial losses, automobile exhaust, sea floor vent, and volcanic emissions. Furthermore, the main sinks of methane in the troposphere, soils or waters via oxidation are also reported, and the corresponding kinetic isotope effects.

  4. Column Averaged CO2, CH4, and CO Mixing Ratios at ARM-SGP

    NASA Astrophysics Data System (ADS)

    Fischer, M. L.; Wunch, D.; Biraud, S.; Abshire, J. B.; Blavier, J. L.; Keppel-Aleks, G.; Kulawik, S. S.; Miller, C. E.; Roehl, C. M.; Payne, V.; Sweeney, C.; Smith, J.; Toon, G. C.; Torn, M. S.; Wennberg, P. O.

    2009-12-01

    We report column-averaged measurements of CO2, CH4, and CO made at the ARM Climate Research Facility in the Southern Great Plains (36.6053 N, 97.4891 W), near Lamont, Oklahoma, USA. Data include multi-year records of midday near-surface (60 m) CO2 and CO mixing ratios, periodic continuous CO2, and flask CO2, CH4, and CO profiles (to ~ 5 km) from a small aircraft, a limited number of flask profiles (to ~ 12 km) from a NASA Lear 25, column CO2, CH4, and CO retrievals made with a sun-tracking Fourier transform spectrometer (FTS) deployed at the SGP site, and estimates of CO2, CH4, and CO from the Tropospheric Emission Spectrometer (TES) on the NASA Aura spacecraft. We compare aircraft measurements with prototype TES retrievals of CO2, TES representative tropospheric values of CH4, and TES CO profile values. We then compare the column-average mixing ratios with the FTS retrievals, and examine the differences in each comparison for seasonality. These results provide an initial evaluation of the TES and FTS retrievals at the ARM-SGP and prepare for future evaluation of CO2 and CH4 retrievals from future satellite missions including GOSAT.

  5. Deep Atmosphere Ammonia Mixing Ratio at Jupiter from the Galileo Probe Mass Spectrometer

    NASA Technical Reports Server (NTRS)

    Mahaffy, P. R.; Niemann, H. B.; Demick, J. E.

    1999-01-01

    New laboratory studies employing the Engineering Unit (EU) of the Galileo Probe Mass Spectrometer (GPMS) have resulted in a substantial reduction in the previously reported upper limit on the ammonia mixing ratio derived from the GPMS experiment at Jupiter. This measurement is complicated by background ammonia contributions in the GPMS during direct atmospheric sampling produced from the preceding gas enrichment experiments. These backgrounds can be quantified with the data from the EU studies when they are carried out in a manner that duplicates the descent profile of pressure and enrichment cell loading. This background is due to the tendency of ammonia to interact strongly with the walls of the mass spectrometer and on release to contribute to the gas being directly directed into the ion source from the atmosphere through a capillary pressure reduction leak. It is evident from the GPMS and other observations that the mixing ratio of ammonia at Jupiter reaches the deep atmosphere value at substantially higher pressures than previously assumed. This is a likely explanation for the previously perceived discrepancy between ammonia values derived from ground based microwave observations and those obtained from attenuation of the Galileo Probe radio signal.

  6. Nitric acid oxide mixing ratio measurements using a rocket launched chemiluminescent instrument

    NASA Technical Reports Server (NTRS)

    Horvath, Jack J.

    1989-01-01

    A total of 18 rocket launched parachute borne nitric oxide instruments were launched from 1977 to 1985. A very precise instrument for the measurement of the nitric oxide mixing ratio was fabricated. No changes were made in the main body of the instruments, i.e., things associated with the reaction volume. Except for the last 4 launches, however, it did not yield the required absolute values that was hoped for. Two major problems were encountered. First, the wrong choice of the background calibration gas, nitrogen, caused the first 10 data sets to be too low in the absolute mixing ratio by nearly the order of 2 to 5 ppbv. The error was realized, and air was substituted for the bias gas measurement. Second, in the desire to extend the measurement to higher altitudes, the problem of contaminating the inlet flow tube with ozone from the reagent gas was encountered. The ozone valve was opened too early in the flight and this caused the pressure in the reaction volume to exceed the pressure at the flow tube entrance, permitting the ozone to migrate backwards. This problem was restricted to an altitude above 45 km.

  7. Optical Properties and Mixing State of Aerosols from Residential Wood Burning and Vehicle Emissions in Central and Southern California

    NASA Astrophysics Data System (ADS)

    Zhang, X.; Cappa, C. D.; Collier, S.; Zhang, Q.; Williams, L. R.; Lee, A.; Abbatt, J.; Russell, L. M.; Liu, J.; Chen, C. L.; Betha, R.

    2015-12-01

    Light-absorbing materials such as black carbon (BC) and brown carbon (BrC) in atmospheric aerosols play important roles in regulating the earth's radiative budget and climate. However, the representations of BC and BrC in state-of-the-art climate models remain highly uncertain, in part due to the poor understanding of their microphysical and optical properties. Direct observations and characterizations of the mixing state and absorption enhancement of ambient aerosols could provide invaluable constraints for current model representations of aerosol radiative effects. Here, we will discuss results from measurements of aerosol light absorption and absorption enhancement (Eabs), using a thermodenuder-absorption method, made during two recent field studies in central and southern California. The winter study took place in Dec/Jan of 2014/2015 in Fresno, CA. This region is severely impacted by particulate matter from local and regional residential biomass burning. The summer study took place in July 2015 in Fontana, CA, a region ~80 km downwind of Los Angeles and strongly impacted by vehicular emissions, and thus provides a sharp contrast to the Fresno study. Eabs of BC particles due to the "lensing" effect from coatings to BC core and/or the presence of BrC will be quantified and compared between the two studies. Additionally, the chemical composition of bulk and the BC-containing particles are determined via a HR-ToF-AMS and a SP-AMS, respectively. Variations in the composition and mixing state of the ambient particles and how these affect the observed Eabs will be examined. The overall measurements suggest a relatively small role for lensing-induced absorption enhancements for ambient particles in these regions.

  8. The Pagami Creek smoke plume after long-range transport to the upper troposphere over Europe - aerosol properties and black carbon mixing state

    NASA Astrophysics Data System (ADS)

    Dahlkötter, F.; Gysel, M.; Sauer, D.; Minikin, A.; Baumann, R.; Seifert, P.; Ansmann, A.; Fromm, M.; Voigt, C.; Weinzierl, B.

    2014-06-01

    During the CONCERT 2011 field experiment with the DLR research aircraft Falcon, an enhanced aerosol layer with particle linear depolarization ratios of 6-8% at 532 nm was observed at altitudes above 10 km over northeast Germany on 16 September 2011. Dispersion simulations with HYSPILT suggest that the elevated aerosol layer originated from the Pagami Creek forest fire in Minnesota, USA, which caused pyro-convective uplift of particles and gases. The 3-4 day-old smoke plume had high total refractory black carbon (rBC) mass concentrations of 0.03-0.35 μg m-3 at standard temperature and pressure (STP) with rBC mass equivalent diameter predominantly smaller than 130 nm. Assuming a core-shell particle structure, the BC cores exhibit very thick (median: 105-136 nm) BC-free coatings. A large fraction of the BC-containing particles disintegrated into a BC-free fragment and a BC fragment while passing through the laser beam of the Single Particle Soot Photometer (SP2). In this study, the disintegration is a result of very thick coatings around the BC cores. This is in contrast to a previous study in a forest-fire plume, where it was hypothesized to be a result of BC cores being attached to a BC-free particle. For the high-altitude forest-fire aerosol layer observed in this study, increased mass specific light-absorption cross sections of BC can be expected due to the very thick coatings around the BC cores, while this would not be the case for the attached-type morphology. We estimate the BC mass import from the Pagami Creek forest fire into the upper troposphere/lower stratosphere (UTLS) region (best estimate: 25 Mg rBC). A comparison to black carbon emission rates from aviation underlines the importance of pyro-convection on the BC load in the UTLS region. Our study provides detailed information on the microphysics and the mixing state of BC in the forest-fire aerosol layer in the upper troposphere that can be used to better understand and investigate the radiative

  9. Mixing state of particles with secondary species by single particle aerosol mass spectrometer in an atmospheric pollution event

    NASA Astrophysics Data System (ADS)

    Xu, Lingling; Chen, Jinsheng

    2016-04-01

    Single particle aerosol mass spectrometer (SPAMS) was used to characterize size distribution, chemical composition, and mixing state of particles in an atmospheric pollution event during 20 Oct. - 5 Nov., 2015 in Xiamen, Southeast China. A total of 533,012 particle mass spectra were obtained and clustered into six groups, comprising of industry metal (4.5%), dust particles (2.6%), carbonaceous species (70.7%), K-Rich particles (20.7%), seasalt (0.6%) and other particles (0.9%). Carbonaceous species were further divided into EC (70.6%), OC (28.5%), and mixed ECOC (0.9%). There were 61.7%, 58.3%, 4.0%, and 14.6% of particles internally mixed with sulfate, nitrate, ammonium and C2H3O, respectively, indicating that these particles had undergone significant aging processing. Sulfate was preferentially mixed with carbonaceous particles, while nitrate tended to mix with metal-containing and dust particles. Compared to clear days, the fractions of EC-, metal- and dust particles remarkably increased, while the fraction of OC-containing particles decreased in pollution days. The mixing state of particles, excepted for OC-containing particles with secondary species was much stronger in pollution days than that in clear days, which revealed the significant influence of secondary particles in atmospheric pollution. The different activity of OC-containing particles might be related to their much smaller aerodynamic diameter. These results could improve our understanding of aerosol characteristics and could be helpful to further investigate the atmospheric process of particles.

  10. Anthropogenic Effects on the Mixing State of Aerosols over Manaus during the Green Ocean Amazon (GoAmazon) Campaign

    NASA Astrophysics Data System (ADS)

    Fraund, M. W.; Pham, D.; Harder, T.; O'Brien, R.; Wang, B.; Laskin, A.; Gilles, M. K.; Moffet, R.

    2015-12-01

    The role that anthropogenic aerosols play in cloud formation is uncertain and contributes largely to the uncertainty in predicting future climate. One region of particular importance is the Amazon rainforest, which accounts for over half of the world's rainforest. During GoAmazon2014/15 IOP2, aerosol samples were collected at multiple sites in and around the rapidly growing industrial city of Manaus in the Amazon basin. Manaus is of scientific interest due to the pristine nature of the surrounding rainforest and the high levels of pollution coming from the city in the form of SO2, NOx, and soot. Some sites, such as the Terrestrial Ecosystem Science center (TES, also designated ZF2) located to the north of Manaus, represent air masses which have not interacted with emissions from the city. The comparison of pristine atmosphere with heavy pollution allows both for the determination of a natural baseline level of pollutants, as well as the study of pollutant's impact on the conversion of biogenic volatile organic compounds to secondary organic aerosols. Towards this goal, samples from ZF2 and other unpolluted sites will be compared to samples from the Atmospheric Radiation Measurement (ARM) climate research facility in Manacapuru (T3), which is southwest (downwind) of Manaus. Spatially resolved spectra were recorded at the sub-particle level using scanning transmission X-ray microscopy (STXM) at the carbon, nitrogen, and oxygen K-absorption edges. Scanning electron microscopy coupled with energy dispersive x-ray spectroscopy (SEM/EDX) was also performed on to characterize higher Z elements. These two techniques together will allow for the mass fraction of atmospherically relevant elements to be determined on a per-particle basis. We will apply established procedures to determine the mixing state index for samples collected at ZF2 and T3 using elemental mass fractions. Preliminary results will be presented which focus on investigating the difference between mixing

  11. Morphology of Mixed Primary and Secondary Organic Particles and the Adsorption of Spectator Organic Gases during Aerosol Formation

    SciTech Connect

    Vaden, Timothy D.; Song, Chen; Zaveri, Rahul A.; Imre, D.; Zelenyuk, Alla

    2010-04-13

    Traditional semi-empirical secondary organic aerosol (SOA) models assume that SOA mixes well with primary organic aerosols (POA), which significantly enhances the modeled SOA yields. These models further assume that the organic compounds in the gas phase do no condense on SOA as it forms. These assumptions were challenged through a detailed experimental investigation of the compositions and morphologies of SOA particles formed during ozonolysis of α-pinene in the presence of dioctyl phthalate (DOP) particles and DOP gas phase component using a single particle mass spectrometer. Ultraviolet (UV) laser depth-profiling experiments were used to characterize different types of mixed SOA/DOP particles: those formed by condensation of the oxidized α-pinene products on size-selected DOP particles and by condensation of DOP on size-selected α-pinene SOA particles. The results of these measurements conclusively show that the hydrophilic SOA and hydrophobic DOP do not mix, but instead form distinct phases. An examination of homogeneously-nucleated SOA particles formed in the presence of DOP shows them to be encapsulated by a thin DOP layer. Thus SOA can adsorb gas-phase DOP even though it has an extremely low vapor pressure (1.3×10-7 Torr), which has significant implications for SOA formation and fate in the atmosphere, where numerous organic compounds with various volatilities are present.

  12. Size distribution and mixing state of refractory black carbon aerosol from a coastal city in South China

    NASA Astrophysics Data System (ADS)

    Wang, Qiyuan; Huang, Ru-Jin; Zhao, Zhuzi; Zhang, Ningning; Wang, Yichen; Ni, Haiyan; Tie, Xuexi; Han, Yongming; Zhuang, Mazhan; Wang, Meng; Zhang, Jieru; Zhang, Xuemin; Dusek, Uli; Cao, Junji

    2016-11-01

    An intensive measurement campaign was conducted in the coastal city of Xiamen, China to investigate the size distribution and mixing state of the refractory black carbon (rBC) aerosol. The average rBC concentration for the campaign, measured with a ground-based single particle soot photometer (SP2), was 2.3 ± 1.7 μg m- 3, which accounted for ~ 4.3% of the PM2.5 mass. A potential source contribution function model indicated that emissions from coastal cities to the southwest were the most important source for the rBC and that shipping traffic was another likely source. The mass size distribution of the rBC particles was mono-modal and approximately lognormal, with a mass median diameter (MMD) of ~ 185 nm. Larger MMDs (~ 195 nm) occurred during polluted conditions compared with non-polluted times (~ 175 nm) due to stronger biomass burning activities during pollution episodes. Uncoated or thinly-coated particles composed the bulk of the rBC aerosol, and on average ~ 31% of the rBC was internally-mixed or thickly-coated. A positive matrix factorization model showed that organic materials were the predominant component of the rBC coatings and that mixing with nitrate increased during pollution conditions. These findings should lead to improvements in the parameterizations used to model the radiative effects of rBC.

  13. Effect of mixing ratio of food waste and rice husk co-digestion and substrate to inoculum ratio on biogas production.

    PubMed

    Haider, Muhammad Rizwan; Zeshan; Yousaf, Sohail; Malik, Riffat Naseem; Visvanathan, Chettiyappan

    2015-08-01

    Aim of this study was to find out suitable mixing ratio of food waste and rice husk for their co-digestion in order to overcome VFA accumulation in digestion of food waste alone. Four mixing ratios of food waste and rice husk with C/N ratios of 20, 25, 30 and 35 were subjected to a lab scale anaerobic batch experiment under mesophilic conditions. Highest specific biogas yield of 584L/kgVS was obtained from feedstock with C/N ratio of 20. Biogas yield decreased with decrease in food waste proportion. Further, fresh cow dung was used as inoculum to investigate optimum S/I ratio with the selected feedstock. In experiment 2, feedstock with C/N ratio 20 was subjected to anaerobic digestion at five S/I ratios of 0.25, 0.5, 1.0, 1.5 and 2.0. Specific biogas yield of 557L/kgVS was obtained at S/I ratio of 0.25. However, VFA accumulation occurred at higher S/I ratios due to higher organic loadings.

  14. Black Carbon, Metal Concentrations and Lead Isotopes Ratios in Aerosols as Tracers of Human and Natural Activities in Northern Vietnam

    NASA Astrophysics Data System (ADS)

    Guinot, B. P.

    2015-12-01

    Atmospheric brown clouds (ABC) observed as widespread layers of brownish haze are regional scale plumes of air pollutants with a hot spot of emission located in East Asia. ABC are mainly composed of aerosol particles such as Black Carbon (BC) emitted to the atmosphere during biomass burning and fossil fuels combustion. The atmospheric lifetime of BC ranges from a few days in wet season up to one month in dry season. The use of stable lead isotopes and 21 elements as tracers of air pollution was applied to identify and characterized the main sources of anthropogenic activities in Asian region. Aerosol samples from Haiphong (North Vietnam) were collected by a high volume sampler for a period of one year from October 2012 to October 2013. Vietnam's 207Pb/206Pb ratios were almost identical to those found for China. Ratios of 207Pb/206Pb ranged from 0.837 to 0.871 which agrees with values previously reported for the last 10 years in China (0.841 - 0.879). No significant variation in isotope ratio was observed during the sampling period, which suggests that there was no large seasonal variation in the isotope ratios of airborne lead. Trajectory analysis showed that almost two third of the air masses originated from East Northeast which implies that China was a major source of lead in atmosphere. Enrichment factor calculations indicated a large influence of coal activity (EF(Al) As = 1982 ± 796, EF(Al) Cd = 972 ± 659, EF(Al) Sb = 1358 ± 930) but the difference between combustion and mining exploitation could not be evidenced. Significant correlations were found between two others groups of elements: As, Cu, Ni, Zn, and Al, Fe K, Co. Wind dilution was effective on metals concentration variation. During the cold and dry season (winter) ambient concentrations were high and variable, during the warm and wet season (summer) concentrations were stable and low. Taken together, these factors also identified industrial and lithogenic activities in the region.

  15. Secondary organic aerosol formation during June 2010 in Central Europe: measurements and modelling studies with a mixed thermodynamic-kinetic approach

    NASA Astrophysics Data System (ADS)

    Langmann, B.; Sellegri, K.; Freney, E.

    2013-10-01

    Until recently secondary organic carbon (SOC) aerosol mass concentrations have been systematically underestimated by three-dimensional atmospheric-chemistry-aerosol models. With a newly proposed concept of aging of organic vapours more realistic model results for organic carbon aerosol mass concentrations could be achieved. Applying a mixed thermodynamic-kinetic approach for SOC aerosol formation shifted the aerosol size distribution towards particles in the cloud condensation nuclei size range, thereby emphasising the importance of SOC aerosol formation schemes for modelling realistic cloud and precipitation formation. The additional importance of hetero-molecular nucleation between H2SO4 and organic vapours remains to be evaluated in three-dimensional atmospheric-chemistry-aerosol models. Here a case study is presented focusing on Puy-de-Dôme, France in June 2010. Even though nucleation events at Puy-de-Dôme were rare during the chosen period of investigation a weak event in the boundary layer could be reproduced by the model when nucleation of low-volatile secondary organic vapour is included. Differences in the model results with and without nucleation of organic vapour are visible in the lower free troposphere over several days of the period. Taking into account nucleation of organic vapour leads to an increase in accumulation mode particles due to coagulation of nucleation and aitken mode particles. Moreover, the measurements indicate a considerable increase in SOC aerosol mass concentration during the measurement campaign, which could be reproduced by modelling using a simplified thermodynamic-kinetic approach for SOC aerosol formation and increased biogenic VOC precursor emissions. Comparison with a thermodynamic SOC aerosol formation approach shows a huge improvement in modelled SOC aerosol mass concentration with the thermodynamic-kinetic approach for SOC aerosol formation and a slight improvement of modelled particle size distribution.

  16. Mixing state of aerosols and direct observation of carbonaceous and marine coatings on African dust by individual particle analysis

    NASA Astrophysics Data System (ADS)

    Deboudt, Karine; Flament, Pascal; ChoëL, Marie; Gloter, Alexandre; Sobanska, Sophie; Colliex, Christian

    2010-12-01

    The mixing state of aerosols collected at M'Bour, Senegal, during the Special Observing Period conducted in January-February 2006 (SOP-0) of the African Monsoon Multidisciplinary Analysis project (AMMA), was studied by individual particle analysis. The sampling location on the Atlantic coast is particularly adapted for studying the mixing state of tropospheric aerosols since it is (1) located on the path of Saharan dust plumes transported westward over the northern tropical Atlantic, (2) influenced by biomass burning events particularly frequent from December to March, and (3) strongly influenced by anthropogenic emissions from polluted African cities. Particle size, morphology, and chemical composition were determined for 12,672 particles using scanning electron microscopy (automated SEM-EDX). Complementary analyses were performed using transmission electron microscopy combined with electron energy loss spectrometry (TEM-EELS) and Raman microspectrometry. Mineral dust and carbonaceous and marine compounds were predominantly found externally mixed, i.e., not present together in the same particles. Binary internally mixed particles, i.e., dust/carbonaceous, carbonaceous/marine, and dust/marine mixtures, accounted for a significant fraction of analyzed particles (from 10.5% to 46.5%). Western Sahara was identified as the main source of mineral dust. Two major types of carbonaceous particles were identified: "tar balls" probably coming from biomass burning emissions and soot from anthropogenic emissions. Regarding binary internally mixed particles, marine and carbonaceous compounds generally formed a coating on mineral dust particles. The carbonaceous coating observed at the particle scale on African dust was evidenced by the combined use of elemental and molecular microanalysis techniques, with the identification of an amorphous rather than crystallized carbon structure.

  17. A new method for the determination of the mixing ratio hydrogen to helium in the giant planets.

    NASA Technical Reports Server (NTRS)

    Gautier, D.; Grossman, K.

    1972-01-01

    By using a numerical iterative method, it is demonstrated that the mixing ratio H2/He on the giant planets can be inferred from spectral measurements of the intensity emitted by these planets in the far infrared range. The method is successfully applied to synthetic spectra of Saturn computed from atmospheric thermal models. The effect of random and systematic measurement errors on the determination of the mixing ratio is also studied.

  18. Anaerobic co-digestion of kitchen waste and pig manure with different mixing ratios.

    PubMed

    Tian, Hailin; Duan, Na; Lin, Cong; Li, Xue; Zhong, Mingzhu

    2015-07-01

    Anaerobic co-digestion of kitchen waste (KW) and pig manure (PM) with seven different PM to KW total solids (TS) ratios of 1:0, 5:1, 3:1, 1:1, 1:3, 1:5 and 0:1 was conducted at mesophilic temperature (35 ± 1 °C) to investigate the feasibility and process performance. The co-digestion of PM and KW was found to be an available way to enhance methane production compared with solo-digestion of PM or KW. The ratio of PM to KW of 1:1 got the highest biodegradability (BDA) of 85.03% and a methane yield of 409.5 mL/gVS. For the co-digestion of KW and PM, there was no obvious inhibition of ammonia nitrogen because it was in an acceptable range from 1380 mg/L to 2020 mg/L in the whole process. However, severe methane inhibition and long lag phase due to the accumulation of volatile fatty acids (VFAs) was observed while the KW content was over 50%, and in the lag phase, propionic acid and butyric acid made up the major constituents of the total VFAs. The technical digestion time (T80: the time it takes to produce 80% of the digester's maximum gas production) of the above 7 ratios was 15, 21, 22, 27, 49, 62 and 61 days, respectively. In this study, a mixing ratio of 1:1 for PM and KW was found to maximize BDA and methane yield, provided a short digestion time and stable digestion performance and was therefore recommended for further study and engineering application.

  19. Phase, morphology, and hygroscopicity of mixed oleic acid/sodium chloride/water aerosol particles before and after ozonolysis.

    PubMed

    Dennis-Smither, Benjamin J; Hanford, Kate L; Kwamena, Nana-Owusua A; Miles, Rachael E H; Reid, Jonathan P

    2012-06-21

    Aerosol optical tweezers are used to probe the phase, morphology, and hygroscopicity of single aerosol particles consisting of an inorganic component, sodium chloride, and a water insoluble organic component, oleic acid. Coagulation of oleic acid aerosol with an optically trapped aqueous sodium chloride droplet leads to formation of a phase-separated particle with two partially engulfed liquid phases. The dependence of the phase and morphology of the trapped particle with variation in relative humidity (RH) is investigated by cavity enhanced Raman spectroscopy over the RH range <5% to >95%. The efflorescence and deliquescence behavior of the inorganic component is shown to be unaffected by the presence of the organic phase. Whereas efflorescence occurs promptly (<1 s), the deliquescence process requires both dissolution of the inorganic component and the adoption of an equilibrium morphology for the resulting two phase particle, occurring on a time-scale of <20 s. Comparative measurements of the hygroscopicity of mixed aqueous sodium chloride/oleic acid droplets with undoped aqueous sodium chloride droplets show that the oleic acid does not impact on the equilibration partitioning of water between the inorganic component and the gas phase or the time response of evaporation/condensation. The oxidative aging of the particles through reaction with ozone is shown to increase the hygroscopicity of the organic component.

  20. Water vapour mixing ratio profiles over Hornsund, Arctic. Intercomparison of lidar and AIRS results

    NASA Astrophysics Data System (ADS)

    Bloch, Magdalena; Karasiński, Grzegorz

    2014-04-01

    Since October 2009, a ground-based Raman lidar system has been deployed to perform a regular, night-time, vertical sounding of a water vapour content in the lower and middle troposphere above Polish Polar Station at Hornsund (77.00°N, 15.55°E, 10 m a.s.l.) in the Arctic. The water vapour mixing ratio profiles were obtained for the atmosphere up to 6 km altitude, based on analysis of inelastic Raman backscattering signals from nitrogen molecules (at 387 nm) and water vapour particles (at 407 nm), calibrated with the data from a local Vaisala's automatic meteorological station. The results obtained for winter seasons in the years 2009-2012 are in a good general agreement with the results obtained from the atmospheric infrared sounder (AIRS) on the Aqua satellite.

  1. Calibration of the Purple Crow Lidar vibrational Raman water-vapour mixing ratio and temperature measurements

    NASA Astrophysics Data System (ADS)

    Argall, P. S.; Sica, R. J.; Bryant, C. R.; Algara-Siller, M.; Schijns, H.

    2007-02-01

    Purple Crow Lidar (PCL) measurements of the vibrational Raman-shifted backscatter from water vapour and nitrogen molecules allows height profiles of the water-vapour mixing ratio to be measured from 500 m up into the lower stratosphere. In addition, the Raman nitrogen measurements allow the determination of temperature profiles from about 10 to 40 km altitude. However, external calibration of these measurements is necessary to compensate for instrumental effects, uncertainties in our knowledge of the relevant molecular cross sections, and atmospheric transmission. A comparison of the PCL-derived water-vapour concentration and temperature profiles with routine radiosonde measurements from Detroit and Buffalo on 37 and 141 nights, respectively, was undertaken to provide this calibration. The calibration is then applied to the measurements and monthly mean-temperature and water-vapour profiles are determined.

  2. Reevaluated martian atmospheric mixing ratios from the mass spectrometer on the Curiosity rover

    NASA Astrophysics Data System (ADS)

    Franz, Heather B.; Trainer, Melissa G.; Wong, Michael H.; Mahaffy, Paul R.; Atreya, Sushil K.; Manning, Heidi L. K.; Stern, Jennifer C.

    2015-05-01

    The Sample Analysis at Mars (SAM) instrument suite of the Mars Science Laboratory (MSL) Curiosity rover is a miniature geochemical laboratory designed to analyze martian atmospheric gases as well as volatiles released by pyrolysis of solid surface materials (Mahaffy et al., 2012). SAM began sampling the martian atmosphere to measure its chemical and isotopic composition shortly after Curiosity landed in Mars' Gale Crater in August 2012 (Mahaffy et al., 2013). Analytical methods and constants required for atmospheric measurements with SAM's quadrupole mass spectrometer (QMS) were provided in a previous contribution (Franz et al., 2014). Review of results obtained through application of these constants to repeated analyses over a full martian year and supporting studies with laboratory instruments offer new insights into QMS performance that allow refinement of the calibration constants and critical reassessment of their estimated uncertainties. This report describes the findings of these studies, provides updated calibration constants for atmospheric analyses with the SAM QMS, and compares volume mixing ratios for the martian atmosphere retrieved with the revised constants to those initially reported (Mahaffy et al., 2013). Sufficient confidence is enabled by the extended data set to support calculation of precise abundances for CO rather than an upper limit. Reanalysis of data acquired on mission sols 45 and 77 (at solar longitudes of 175° and 193°, respectively) with the revised constants leads to the following average volume mixing ratios: CO2 0.957(±0.016), N2 0.0203(±0.0003), Ar 0.0207(±0.0002), O2 1.73(±0.06)×10-3, CO 7.49(±0.026)×10-4.

  3. A conceptual framework to quantify the influence of convective boundary layer development on carbon dioxide mixing ratios

    NASA Astrophysics Data System (ADS)

    Pino, D.; Vilà-Guerau de Arellano, J.; Peters, W.; Schroter, J.; van Heerwaarden, C. C.; Krol, M.

    2011-12-01

    Interpretation of observed diurnal carbon dioxide (CO2) mixing ratios near the surface requires knowledge of the local dynamics of the planetary boundary layer. In this paper, we quantify the relationship between the boundary layer dynamics and the CO2 budget in convective conditions through a newly derived set of analytical equations. From these equations, we are able to quantify how uncertainties in boundary layer dynamical variables or in the morning CO2 distribution in the mixed-layer or in the free atmosphere influence the bulk CO2 mixing ratio. We find that the largest uncertainty incurred on the mid-day CO2 mixing ratio comes from the prescribed early morning CO2 mixing ratios in the stable boundary layer, and in the free atmosphere. Errors in these values influence CO2 mixing ratios inversely proportional to the boundary layer depth (h), just like uncertainties in the assumed initial boundary layer depth and surface CO2 flux. The influence of uncertainties in the boundary layer depth itself are one order of magnitude smaller. If we "invert" the problem and calculate CO2 surface exchange from observed or simulated CO2 mixing ratios, the sensitivities to errors in boundary layer dynamics also invert: they become linearly proportional to the boundary layer depth. We demonstrate these relations for a typical well characterized situation at the Cabauw tower in the Netherlands, and conclude that knowledge of the temperature and carbon dioxide vertical profiles in the early morning are of vital importance to correctly interpret observed CO2 mixing ratios during midday.

  4. A conceptual framework to quantify the influence of convective boundary layer development on carbon dioxide mixing ratios

    NASA Astrophysics Data System (ADS)

    Pino, D.; Vilà-Guerau de Arellano, J.; Peters, W.; Schröter, J.; van Heerwaarden, C. C.; Krol, M. C.

    2012-03-01

    Interpretation of observed diurnal carbon dioxide (CO2) mixing ratios near the surface requires knowledge of the local dynamics of the planetary boundary layer. In this paper, we study the relationship between the boundary layer dynamics and the CO2 budget in convective conditions through a newly derived set of analytical equations. From these equations, we are able to quantify how uncertainties in boundary layer dynamical variables or in the morning CO2 distribution in the mixed-layer or in the free atmosphere (FA) influence the bulk CO2 mixing ratio. We find that the largest uncertainty incurred on the mid-day CO2 mixing ratio comes from the prescribed early morning CO2 mixing ratios in the stable boundary layer, and in the free atmosphere. Errors in these values influence CO2 mixing ratios inversely proportional to the boundary layer depth (h), just like uncertainties in the assumed initial boundary layer depth and surface CO2 flux. The influence of uncertainties in the boundary layer depth itself is one order of magnitude smaller. If we "invert" the problem and calculate CO2 surface exchange from observed or simulated CO2 mixing ratios, the sensitivities to errors in boundary layer dynamics also invert: they become linearly proportional to the boundary layer depth. We demonstrate these relations for a typical well characterized situation at the Cabauw site in The Netherlands, and conclude that knowledge of the temperature and carbon dioxide profiles of the atmosphere in the early morning are of vital importance to correctly interpret observed CO2 mixing ratios during midday.

  5. Variations in the methanesulfonate to sulfate molar ratio in submicrometer marine aerosol particles over the south Pacific Ocean

    NASA Technical Reports Server (NTRS)

    Bates, Timothy S.; Calhoun, Julie A.; Quinn, Patricia K.

    1992-01-01

    Seawater concentrations of dimethylsulfide (DMS) and atmospheric concentrations of DMS, sulfur dioxide, methanesulfonate (MSA), and non-sea-salt (nss) sulfate were measured over the eastern Pacific Ocean between 105 deg and 110 deg W from 20 deg N to 60 deg S during February and March 1989. Although the samples collected in the Southern Hemisphere appear to be of marine origin, no significant correlation was found between the latitudinal distributions of DMS, SO2, MSA, and nss SO4(2-). However, an inverse correlation was found between atmospheric temperature and the MSA to nss SO4(2-) molar ratio in submicrometer aerosol particles with a decrease in temperature corresponding to an increase in the molar ratio. Although this trend is consistent with laboratory results indicating the favored production of MSA at lower temperatures, it is contrary to Southern Hemisphere baseline station data. This suggests either a decrease in the supply of DMS relative to nonmarine sources of nss SO4(2-) at the baseline stations in winter or additional mechanisms that affect the relative production of MSA and nss SO4(2-).

  6. 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.

  7. Reactive bromine chemistry in Mount Etna's volcanic plume: the influence of total Br, high-temperature processing, aerosol loading and plume-air mixing

    NASA Astrophysics Data System (ADS)

    Roberts, T. J.; Martin, R. S.; Jourdain, L.

    2014-10-01

    Volcanic emissions present a source of reactive halogens to the troposphere, through rapid plume chemistry that converts the emitted HBr to more reactive forms such as BrO. The nature of this process is poorly quantified, yet is of interest in order to understand volcanic impacts on the troposphere, and infer volcanic activity from volcanic gas measurements (i.e. BrO / SO2 ratios). Recent observations from Etna report an initial increase and subsequent plateau or decline in BrO / SO2 ratios with distance downwind. We present daytime PlumeChem model simulations that reproduce and explain the reported trend in BrO / SO2 at Etna including the initial rise and subsequent plateau. Suites of model simulations also investigate the influences of volcanic aerosol loading, bromine emission, and plume-air mixing rate on the downwind plume chemistry. Emitted volcanic HBr is converted into reactive bromine by autocatalytic bromine chemistry cycles whose onset is accelerated by the model high-temperature initialisation. These rapid chemistry cycles also impact the reactive bromine speciation through inter-conversion of Br, Br2, BrO, BrONO2, BrCl, HOBr. We predict a new evolution of Br speciation in the plume. BrO, Br2, Br and HBr are the main plume species near downwind whilst BrO and HOBr are present further downwind (where BrONO2 and BrCl also make up a minor fraction). BrNO2 is predicted to be only a relatively minor plume component. The initial rise in BrO / SO2 occurs as ozone is entrained into the plume whose reaction with Br promotes net formation of BrO. Aerosol has a modest impact on BrO / SO2 near-downwind (< ~6 km, ~10 min) at the relatively high loadings considered. The subsequent decline in BrO / SO2 occurs as entrainment of oxidants HO2 and NO2 promotes net formation of HOBr and BrONO2, whilst the plume dispersion dilutes volcanic aerosol so slows the heterogeneous loss rates of these species. A higher volcanic aerosol loading enhances BrO / SO2 in the (> 6 km

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

    NASA Technical Reports Server (NTRS)

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

    1993-01-01

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

  9. Optical, size and mass properties of mixed type aerosols in Greece and Romania as observed by synergy of lidar and sunphotometers in combination with model simulations: a case study.

    PubMed

    Papayannis, A; Nicolae, D; Kokkalis, P; Binietoglou, I; Talianu, C; Belegante, L; Tsaknakis, G; Cazacu, M M; Vetres, I; Ilic, L

    2014-12-01

    A coordinated experimental campaign aiming to study the aerosol optical, size and mass properties was organized in September 2012, in selected sites in Greece and Romania. It was based on the synergy of lidar and sunphotometers. In this paper we focus on a specific campaign period (23-24 September), where mixed type aerosols (Saharan dust, biomass burning and continental) were confined from the Planetary Boundary Layer (PBL) up to 4-4.5 km height. Hourly mean linear depolarization and lidar ratio values were measured inside the dust layers, ranging from 13 to 29 and from 44 to 65sr, respectively, depending on their mixing status and the corresponding air mass pathways over Greece and Romania. During this event the columnar Aerosol Optical Depth (AOD) values ranged from 0.13 to 0.26 at 532 nm. The Lidar/Radiometer Inversion Code (LIRIC) and the Polarization Lidar Photometer Networking (POLIPHON) codes were used and inter-compared with regards to the retrieved aerosol (fine and coarse spherical/spheroid) mass concentrations, showing that LIRIC generally overestimates the aerosol mass concentrations, in the case of spherical particles. For non-spherical particles the difference in the retrieved mass concentration profiles from these two codes remained smaller than ±20%. POLIPHON retrievals showed that the non-spherical particles reached concentrations of the order of 100-140 μg/m(3) over Romania compared to 50-75 μg/m(3) over Greece. Finally, the Dust Regional Atmospheric Model (DREAM) model was used to simulate the dust concentrations over the South-Eastern Europe.

  10. Modulation of aerosol radiative forcing due to mixing state in clear and cloudy-sky: A case study from Delhi National Capital Region, India

    NASA Astrophysics Data System (ADS)

    Srivastava, Parul; Dey, Sagnik; Srivastava, Atul K.; Singh, Sachchidanand; Tiwari, Suresh; Agarwal, Poornima

    2016-04-01

    Aerosol properties change with the change in mixing state of aerosols and therefore it is a source of uncertainty in estimated aerosol radiative forcing (ARF) from observations or by models assuming a specific mixing state. The problem is important in the Indo-Gangetic Basin, Northern India, where various aerosol types mix and show strong seasonal variations. Quantifying the modulation of ARF by mixing state is hindered by lack of knowledge about proper aerosol composition. Hence, first a detailed chemical composition analysis of aerosols for Delhi National capital region (NCR) is carried out. Aerosol composition is arranged quantitatively into five major aerosol types - accumulation dust, coarse dust, water soluble (WS), water insoluble (WINS), and black carbon (BC) (directly measured by Athelometer). Eight different mixing cases - external mixing, internal mixing, and six combinations of core- shell mixing (BC over dust, WS over dust, WS over BC, BC over WS, WS over WINS, and BC over WINS; each of the combinations externally mixed with other species) have been considered. The spectral aerosol optical properties - extinction coefficient, single scattering albedo (SSA) and asymmetry parameter (g) for each of the mixing cases are calculated and finally 'clear-sky' and 'cloudy-sky' ARF at the top-of-the-atmosphere (TOA) and surface are estimated using a radiative transfer model. Comparison of surface-reaching flux for each of the cases with MERRA downward shortwave surface flux reveals the most likely mixing state. 'BC-WINS+WS+Dust' show least deviation relative to MERRA during the pre-monsoon (MAMJ) and monsoon (JAS) seasons and hence is the most probable mixing states. During the winter season (DJF), 'BC-Dust+WS+WINS' case shows the closest match with MERRA, while external mixing is the most probable mixing state in the post-monsoon season (ON). Lowest values for both TOA and surface 'clear-sky' ARF is observed for 'BC-WINS+WS+ Dust' mixing case. TOA ARF is 0.28±2

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

    SciTech Connect

    Jackson, Robert C.; McFarquhar, Greg; Korolev, Alexei; Earle, Michael; Liu, Peter S.; Lawson, R. P.; Brooks, Sarah D.; Wolde, Mengistu; Laskin, Alexander; Freer, Matthew

    2012-08-14

    Cloud and aerosol data acquired by the National Research Council of Canada (NRC) Convair-580 aircraft in, above, and below single-layer arctic stratocumulus cloud during the Indirect and Semi-Direct Aerosol Campaign (ISDAC) in April 2008 were used to test three aerosol indirect effects hypothesized to act in mixed-phase clouds: the riming indirect effect, the glaciation indirect effect, and the cold second indirect effect. The data showed a correlation of R= 0.75 between liquid drop number concentration, Nliq, inside cloud and ambient aerosol number concentration NPCASP below cloud. This, combined with increasing liquid water content LWC with height above cloud base and the nearly constant profile of Nliq, suggested that liquid drops were nucleated from aerosol at cloud base. No strong evidence of a riming indirect effect was observed, but a strong correlation of R = 0.69 between ice crystal number concentration Ni and NPCASP above cloud was noted. Increases in ice nuclei (IN) concentration with NPCASP above cloud combined with the subadiabatic LWC profiles suggest possible mixing of IN from cloud top consistent with the glaciation indirect effect. The higher Nice and lower effective radius rel for the more polluted ISDAC cases compared to data collected in cleaner single-layer stratocumulus conditions during the Mixed-Phase Arctic Cloud Experiment is consistent with the operation of the cold second indirect effect. However, more data in a wider variety of meteorological and surface conditions, with greater variations in aerosol forcing, are required to identify the dominant aerosol forcing mechanisms in mixed-phase arctic clouds.

  12. Angular and Seasonal Variation of Spectral Surface Reflectance Ratios: Implications for the Remote Sensing of Aerosol over Land

    NASA Technical Reports Server (NTRS)

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

    1999-01-01

    We obtain valuable information on the angular and seasonal variability of surface reflectance using a hand-held spectrometer from a light aircraft. The data is used to test a procedure that allows us to estimate visible surface reflectance from the longer wavelength 2.1 micrometer channel (mid-IR). Estimating or avoiding surface reflectance in the visible is a vital first step in most algorithms that retrieve aerosol optical thickness over land targets. The data indicate that specular reflection found when viewing targets from the forward direction can severely corrupt the relationships between the visible and 2.1 micrometer reflectance that were derived from nadir data. There is a month by month variation in the ratios between the visible and the mid-IR, weakly correlated to the Normalized Difference Vegetation Index (NDVI). If specular reflection is not avoided, the errors resulting from estimating surface reflectance from the mid-IR exceed the acceptable limit of DELTA-rho approximately 0.01 in roughly 40% of the cases, using the current algorithm. This is reduced to 25% of the cases if specular reflection is avoided. An alternative method that uses path radiance rather than explicitly estimating visible surface reflectance results in similar errors. The two methods have different strengths and weaknesses that require further study.

  13. Effects of volatile solid concentration and mixing ratio on hydrogen production by co-digesting molasses wastewater and sewage sludge.

    PubMed

    Lee, Jung-Yeol; Wee, Daehyun; Cho, Kyung-Suk

    2014-11-28

    Co-digesting molasses wastewater and sewage sludge was evaluated for hydrogen production by response surface methodology (RSM). Batch experiments in accordance with various dilution ratios (40- to 5-fold) and waste mixing composition ratios (100:0, 80:20, 60:40, 40:60, 20:80, and 0:100, on a volume basis) were conducted. Volatile solid (VS) concentration strongly affected the hydrogen production rate and yield compared with the waste mixing ratio. The specific hydrogen production rate was predicted to be optimal when the VS concentration ranged from 10 to 12 g/l at all the mixing ratios of molasses wastewater and sewage sludge. A hydrogen yield of over 50 ml H2/g VS(removed) was obtained from mixed waste of 10% sewage sludge and 10 g/l VS (about 10-fold dilution ratio). The optimal chemical oxygen demand/ total nitrogen ratio for co-digesting molasses wastewater and sewage sludge was between 250 and 300 with a hydrogen yield above 20 ml H2/g VS(removed).

  14. Mobile lidar system for measurement of water vapor mixing ratio and ozone number density

    NASA Technical Reports Server (NTRS)

    Whiteman, D.

    1988-01-01

    The Water Vapor Lidar was modified and extended to make differential absorption measurements of ozone. Water vapor measurements make use of a weak molecular scattering process known as Raman scattering. It is characterized by a shift in wavelength of the scattered beam of light relative to the incident one. Some of the energy of the incident photon is converted to vibrational or rotational energy within the molecule leaving the scattered photon shifted to a slightly longer wavelength. When performing water vapor measurements, profiles are acquired of water vapor mixing ratio from near the ground to beyond 7 km every 2 minutes. By forming a color composite image of the individual profiles, the spatial and temporal evolution of water vapor is visible with vertical resolution of 75 to 150m and temporal resolution of 2 minutes. The ozone lidar is intended for use as a cross calibration facility for other stationary ozone lidar systems. The ozone measurement employs the technique known as differential absorption. The backscattered laser radiation from two different wavelengths is measured. Successful measurements of 308 nm returns were made from 80 km with an averaging period of 6 hours. Using these data and a standard atmosphere density curve, an ozone number density profile was made which agrees very well with the standard ozone curve between 20 and 40 km.

  15. O/M RATIO MEASUREMENT IN PURE AND MIXED OXIDE FULES - WHERE ARE WE NOW?

    SciTech Connect

    J. RUBIN; ET AL

    2000-12-01

    The oxygen-to-metal (O/M) ratio is one of the most critical parameters of nuclear fuel fabrication, and its measurement is closely monitored for manufacturing process control and to ensure the service behavior of the final product. Thermogravimetry is the most widely used method, the procedure for which has remained largely unchanged since its development some thirty years ago. It was not clear to us, however, that this method is still the optimum one in light of advances in instrumentation, and in the current regulatory environment, particularly with regard to waste management and disposal. As part of the MOX fuel fabrication program at Los Alamos, we conducted a comprehensive review of methods for O/M measurements in UO{sub 2}, PuO{sub 2} and mixed oxide fuels for thermal reactors. A concerted effort was made to access information not available in the open literature. We identified approximately thirty five experimental methods that (a) have been developed with the intent of measuring O/M, (b) provided O/M indirectly by suitable reduction of the measured data, or (c) could provide O/M data with suitable data reduction or when combined with other methods. We will discuss the relative strengths and weaknesses of these methods in their application to current routine and small-lot production environment.

  16. On the cross-sensitivity between water vapor mixing ratio and stable isotope measurements of in-situ analyzers

    NASA Astrophysics Data System (ADS)

    Parkes, Stephen; Wang, Lixin; McCabe, Matthew

    2015-04-01

    In recent years there has been an increasing amount of water vapor stable isotope data collected using in-situ instrumentation. A number of papers have characterized the performance of these in-situ analyzers and suggested methods for calibrating raw measurements. The cross-sensitivity of the isotopic measurements on the mixing ratio has been shown to be a major uncertainty and a variety of techniques have been suggested to characterize this inaccuracy. However, most of these are based on relating isotopic ratios to water vapor mixing ratios from in-situ analyzers when the mixing ratio is varied and the isotopic composition kept constant. An additional correction for the span of the isotopic ratio scale is then applied by measuring different isotopic standards. Here we argue that the water vapor cross-sensitivity arises from different instrument responses (span and offset) of the parent H2O isotope and the heavier isotopes, rather than spectral overlap that could cause a true variation in the isotopic ratio with mixing ratio. This is especially relevant for commercial laser optical instruments where absorption lines are well resolved. Thus, the cross-sensitivity determined using more conventional techniques is dependent on the isotopic ratio of the standard used for the characterization, although errors are expected to be small. Consequently, the cross-sensitivity should be determined by characterizing the span and zero offset of each isotope mixing ratio. In fact, this technique makes the span correction for the isotopic ratio redundant. In this work we model the impact of changes in the span and offset of the heavy and light isotopes and illustrate the impact on the cross-sensitivity of the isotopic ratios on water vapor. This clearly shows the importance of determining the zero offset for the two isotopes. The cross-sensitivity of the isotopic ratios on water vapor is then characterized by determining the instrument response for the individual isotopes for a

  17. Simultaneous Engineering of the Substrate Temperature and Mixing Ratio to Improve the Performance of Organic Photovoltaic Cells.

    PubMed

    Song, Hyung-Jun; Roh, Jeongkyun; Lee, Changhee

    2016-05-01

    In this study, we investigated the effect of the donor/acceptor mixing ratio and the substrate temperature (T(SUB)) during the co-deposition process on the performance of bulk heterojunction organic photovoltaic cells. We found that the ratio of dispersed donor islands (less than 10 nm), which hinders charge carrier transport, increased as the donor concentration (C(D)) increased in the film processed at room temperature. By contrast, the donor cluster (larger than 10 nm), providing percolation paths for the carriers, was enlarged in the film containing a high C(D) fabricated at high T(SUB) (70 degrees C). This enhanced phase separation in the mixed layer led to an improved fill factor and a decreased activation energy of the short-circuit current (J(SC)). Therefore, we demonstrated a 23% improvement in the device performance by employing an elevated T(SUB) and optimized mixing ratio in comparison with the device fabricated at room temperature.

  18. Weekly and Seasonal Trends in the Diurnal Variation of CO2 Mixing Ratio in Pasadena, CA

    NASA Astrophysics Data System (ADS)

    Newman, S.; Stolper, E. M.

    2009-12-01

    Diurnal variations in CO2 mixing ratio ([CO2]) in urban areas reflect changing proportions of biogenic and anthropogenic sources and changes in meteorological conditions (e.g., London, England: Rigby et al., 2008, Atm. Env. 42, 8943-8953). We have monitored [CO2] in Pasadena, CA almost continuously since 2001 using an infrared gas analyzer. In a typical day there is a low [CO2] plateau at about ~10 AM-4 PM (all times given as Pacific Standard Time) and a high [CO2] plateau at ~9 PM-3 AM, as observed previously for both CO (e.g., Riverside, CA: Gentner et al., 2009, Env. Sci. Tech. 43, 4247-4252) and CO2 (e.g., Vancouver, British Columbia, Canada: Reid and Steyn, 1997, Atm. Env. 31, 3101-3114; Phoenix, AZ: Idso et al., 2002, Atm. Env. 36, 1655-1660; Salt Lake City, UT: Pataki et al., 2007, Oecolog. 152, 307-322; London, England: Rigby et al., 2008). The midday low and nighttime high in [CO2] are probably due to draw-down by photosynthesis during daylight hours and respiration at night, accompanied by diurnal changes in the mixed-layer depth resulting from formation and destruction of a nocturnal temperature inversion layer (e.g., Reid and Steyn, 1997). The amplitude of the diurnal variation in Pasadena ranges from ~20 ppm in June to ~70 ppm in December. We typically observe a maximum in [CO2] at ~5-9 AM on weekday mornings. This peak is smaller on weekends, generally being smallest on Sundays. This morning [CO2] peak coincides with increased traffic on surface streets in Los Angeles due to weekday morning rush hour (Chinkin et al., 2003, J. Air Waste Mgmt. Assoc. 53, 829-843) it has also been observed by Reid and Steyn (1997) and Idso, et al. (2002 ) in Vancouver, BC, Canada, and Phoenix, AZ, respectively. There is no corresponding peak that can be associated with afternoon rush hour, perhaps because the time period of the afternoon commute is ill-defined in Pasadena and/or increased emissions from this time of day contribute to the evening increase in [CO2] along

  19. Large Engine Technology (LET) Task XXXVII Low-Bypass Ratio Mixed Turbofan Engine Subsonic Jet Noise Reduction Program Test Report

    NASA Technical Reports Server (NTRS)

    Hauser, Joseph R.; Zysman, Steven H.; Barber, Thomas J.

    2001-01-01

    NASA Glenn Research Center supported a three year effort to develop the technology for reducing jet noise from low-bypass ratio engines. This effort concentrated on both analytical and experimental approaches using various mixer designs. CFD and MGB predictions are compared with LDV and noise data, respectively. While former predictions matched well with data, experiment shows a need for improving the latter predictions. Data also show that mixing noise can be sensitive to engine hardware upstream of the mixing exit plane.

  20. Single particle characterization of biomass burning organic aerosol (BBOA): evidence for non-uniform mixing of high molecular weight organics and potassium

    NASA Astrophysics Data System (ADS)

    Lee, A. K. Y.; Willis, M. D.; Healy, R. M.; Wang, J. M.; Jeong, C.-H.; Wenger, J. C.; Evans, G. J.; Abbatt, J. P. D.

    2015-11-01

    Biomass burning is a major source of black carbon (BC) and primary organic aerosol globally. In particular, biomass burning organic aerosol (BBOA) is strongly associated with atmospheric brown carbon (BrC) that absorbs near ultraviolet and visible light, resulting in significant impacts on regional visibility degradation and radiative forcing. The mixing state of BBOA can play a critical role in the prediction of aerosol optical properties. In this work, single particle measurements from a soot-particle aerosol mass spectrometer coupled with a light scattering module (LS-SP-AMS) were performed to examine the mixing state of BBOA, refractory black carbon (rBC) and potassium (K+, a tracer for biomass burning aerosol) in an air mass influenced by aged biomass burning. Cluster analysis of single particle measurements identified five BBOA-related particle types. rBC accounted for 3-14 w.t. % of these particle types on average. Only one particle type exhibited a strong ion signal for K+, with mass spectra characterized by low molecular weight organic species. The remaining four particle types were classified based on the apparent molecular weight of the BBOA constituents. Two particle types were associated with low potassium content and significant amounts of high molecular weight (HMW) organic compounds. Our observations indicate non-uniform mixing of particles within a biomass burning plume in terms of molecular weight and illustrate that HMW BBOA can be a key contributor to low-volatility BrC observed in BBOA particles.

  1. Probing the impact of different aerosol sources on cloud microphysics and precipitation through in-situ measurements of chemical mixing state

    NASA Astrophysics Data System (ADS)

    Prather, K. A.; Suski, K.; Cazorla, A.; Cahill, J. F.; Creamean, J.; Collins, D. B.; Heymsfield, A.; Roberts, G. C.; DeMott, P. J.; Sullivan, R. C.; Rosenfeld, D.; Comstock, J. M.; Tomlinson, J. M.

    2011-12-01

    Aerosol particles play a crucial role in affecting cloud processes by serving as cloud nuclei. However, our understanding of which particles actually form cloud and ice nuclei limits our ability to treat aerosols properly in climate models. In recent years, it has become possible to measure the chemical composition of individual cloud nuclei within the clouds using on-line mass spectrometry. In-situ high time resolution chemistry can now be compared with cloud physics measurements to directly probe the impact of aerosol chemistry on cloud microphysics. This presentation will describe results from two recent field campaigns, CalWater in northern California and ICE-T in the western Caribbean region. Ground-based and aircraft measurements will be presented of aerosol mixing state, cloud microphysics, and meteorology. Results from single particle mass spectrometry will show the sources of the cloud seeds, including dust, biomass burning, sea spray, and biological particles. Details will be provided on how we are now able to probe the sources and cycling of atmospheric aerosols by measuring individual aerosols, cloud nuclei, and precipitation chemistry. The important role of dust, both Asian and African, and bioparticles in forming ice nuclei will be discussed. Finally, a summary will be provided discussing how these new in-situ measurements are being used to advance our understanding of complex atmospheric processes, and improve our understanding of aerosol impacts on climate.

  2. Fluid mixing and recycling during Pyrenean thrusting: evidence from fluid inclusion halogen ratios

    NASA Astrophysics Data System (ADS)

    McCaig, A. M.; Tritlla, J.; Banks, D. A.

    2000-10-01

    Syntectonic fluids have been sampled through fluid inclusion microthermometry and crush-leach analyses (cations and halogens) from a 50 km N-S transect through the central-southern Pyrenees. The fluid inclusions are contained in syntectonic quartz veins in Triassic redbeds, Cretaceous carbonates and Hercynian basement rocks, with some calcite and dolomite data from limestones and evaporites in more external parts of the belt. The main datasets come from (1) Alpine shear zones cutting the Néouvielle granodiorite in the Hercynian Axial Zone at the north end of the transect; (2) An imbricate zone beneath the Alpine Gavarnie Thrust at the Pic de Port Vieux; (3) Several localities in the footwall and hangingwall of the Gavarnie Thrust on the southern margin of the Axial Zone. The inclusion fluids generally decrease in salinity from 27-35% at the northern end of the transect to 7-22% on the southern margin of the Axial Zone. The majority of the inclusions have Cl/Br ratios lower than seawater and are interpreted as relict fluids after seawater evaporation and halite precipitation in the upper Trias. This interpretation is supported by Cl-Br-Na systematics, which are consistent with a change from halite to halite + sylvite precipitation with progressive evaporation. Fluids in the basement shear zones are interpreted to have essentially the same evaporitic origin as those still contained in sedimentary formations, although it is possible that final concentration of brines in the Néouvielle Massif involved retrograde hydration reactions with removal of water by precipitation of hydrous minerals. The fluids are also very similar in salinity and halogen chemistry to those found in veins associated with Mesozoic Pb-Zn-F deposits which predate the thrusting. The lower salinities seen at the southern margin of the Axial Zone are interpreted to reflect mixing of the brines with a higher level fluid (connate or meteoric water) circulating within the Mesozoic carbonates of the

  3. Aerosol Classification from High Spectral Resolution Lidar Measurements

    NASA Astrophysics Data System (ADS)

    Burton, S. P.; Hair, J. W.; Ferrare, R. A.; Hostetler, C. A.; Kahnert, M.; Vaughan, M. A.; Cook, A. L.; Harper, D. B.; Berkoff, T.; Seaman, S. T.; Collins, J. E., Jr.; Fenn, M. A.; Rogers, R. R.

    2015-12-01

    The NASA Langley airborne High Spectral Resolution Lidars, HSRL-1 and HSRL-2, have acquired large datasets of vertically resolved aerosol extinction, backscatter, and depolarization during >30 airborne field missions since 2006. The lidar measurements of aerosol intensive parameters like lidar ratio and color ratio embed information about intrinsic aerosol properties, and are combined to qualitatively classify HSRL aerosol measurements into aerosol types. Knowledge of aerosol type is important for assessing aerosol radiative forcing, and can provide useful information for source attribution studies. However, atmospheric aerosol is frequently not a single pure type, but instead is a mixture, which affects the optical and radiative properties of the aerosol. We show that aerosol intensive parameters measured by lidar can be understood using mixing rules for cases of external mixing. Beyond coarse classification and mixing between classes, variations in the lidar aerosol intensive parameters provide additional insight into aerosol processes and composition. This is illustrated by depolarization measurements at three wavelengths, 355 nm, 532 nm, and 1064 nm, made by HSRL-2. Particle depolarization ratio is an indicator of non-spherical particles. Three cases each have a significantly different spectral dependence of the depolarization ratio, related to the size of the depolarizing particles. For two dust cases, large non-spherical particles account for the depolarization of the lidar light. The spectral dependence reflects the size distribution of these particles and reveals differences in the transport histories of the two plumes. For a smoke case, the depolarization is inferred to be due to the presence of small coated soot aggregates. Interestingly, the depolarization at 355 nm is similar for this smoke case compared to the dust cases, having potential implications for the upcoming EarthCARE satellite, which will measure particle depolarization ratio only at 355 nm.

  4. Ratio

    NASA Astrophysics Data System (ADS)

    Webster, Nathan A. S.; Pownceby, Mark I.; Madsen, Ian C.; Studer, Andrew J.; Manuel, James R.; Kimpton, Justin A.

    2014-12-01

    Effects of basicity, B (CaO:SiO2 ratio) on the thermal range, concentration, and formation mechanisms of silico-ferrite of calcium and aluminum (SFCA) and SFCA-I iron ore sinter bonding phases have been investigated using an in situ synchrotron X-ray diffraction-based methodology with subsequent Rietveld refinement-based quantitative phase analysis. SFCA and SFCA-I phases are the key bonding materials in iron ore sinter, and improved understanding of the effects of processing parameters such as basicity on their formation and decomposition may assist in improving efficiency of industrial iron ore sintering operations. Increasing basicity significantly increased the thermal range of SFCA-I, from 1363 K to 1533 K (1090 °C to 1260 °C) for a mixture with B = 2.48, to ~1339 K to 1535 K (1066 °C to 1262 °C) for a mixture with B = 3.96, and to ~1323 K to 1593 K (1050 °C to 1320 °C) at B = 4.94. Increasing basicity also increased the amount of SFCA-I formed, from 18 wt pct for the mixture with B = 2.48 to 25 wt pct for the B = 4.94 mixture. Higher basicity of the starting sinter mixture will, therefore, increase the amount of SFCA-I, considered to be more desirable of the two phases. Basicity did not appear to significantly influence the formation mechanism of SFCA-I. It did, however, affect the formation mechanism of SFCA, with the decomposition of SFCA-I coinciding with the formation of a significant amount of additional SFCA in the B = 2.48 and 3.96 mixtures but only a minor amount in the highest basicity mixture. In situ neutron diffraction enabled characterization of the behavior of magnetite after melting of SFCA produced a magnetite plus melt phase assemblage.

  5. Polar and non-polar organic aerosols from large-scale agricultural-waste burning emissions in Northern India: Implications to organic mass-to-organic carbon ratio.

    PubMed

    Rajput, Prashant; Sarin, M M

    2014-05-01

    This study focuses on characteristics of organic aerosols (polar and non-polar) and total organic mass-to-organic carbon ratio (OM/OC) from post-harvest agricultural-waste (paddy- and wheat-residue) burning emissions in Northern India. Aerosol samples from an upwind location (Patiala: 30.2°N, 76.3°E) in the Indo-Gangetic Plain were analyzed for non-polar and polar fractions of organic carbon (OC1 and OC2) and their respective mass (OM1 and OM2). On average, polar organic aerosols (OM2) contribute nearly 85% of the total organic mass (OM) from the paddy- and wheat-residue burning emissions. The water-soluble-OC (WSOC) to OC2 ratio, within the analytical uncertainty, is close to 1 from both paddy- and wheat-residue burning emissions. However, temporal variability and relatively low WSOC/OC2 ratio (Av: 0.67±0.06) is attributed to high moisture content and poor combustion efficiency during paddy-residue burning, indicating significant contribution (∼30%) of aromatic carbon to OC2. The OM/OC ratio for non-polar (OM1/OC1∼1.2) and polar organic aerosols (OM2/OC2∼2.2), hitherto unknown for open agricultural-waste burning emissions, is documented in this study. The total OM/OC ratio is nearly identical, 1.9±0.2 and 1.8±0.2, from paddy- and wheat-residue burning emissions.

  6. Comparison of MADE3-simulated and observed aerosol distributions with a focus on aerosol vertical profiles

    NASA Astrophysics Data System (ADS)

    Kaiser, Christopher; Hendricks, Johannes; Righi, Mattia; Jöckel, Patrick

    2016-04-01

    The reliability of aerosol radiative forcing estimates from climate models depends on the accuracy of simulated global aerosol distribution and composition, as well as on the models' representation of the aerosol-cloud and aerosol-radiation interactions. To help improve on previous modeling studies, we recently developed the new aerosol microphysics submodel MADE3 that explicitly tracks particle mixing state in the Aitken, accumulation, and coarse mode size ranges. We implemented MADE3 into the global atmospheric chemistry general circulation model EMAC and evaluated it by comparison of simulated aerosol properties to observations. Compared properties include continental near-surface aerosol component concentrations and size distributions, continental and marine aerosol vertical profiles, and nearly global aerosol optical depth. Recent studies have shown the specific importance of aerosol vertical profiles for determination of the aerosol radiative forcing. Therefore, our focus here is on the evaluation of simulated vertical profiles. The observational data is taken from campaigns between 1990 and 2011 over the Pacific Ocean, over North and South America, and over Europe. The datasets include black carbon and total aerosol mass mixing ratios, as well as aerosol particle number concentrations. Compared to other models, EMAC with MADE3 yields good agreement with the observations - despite a general high bias of the simulated mass mixing ratio profiles. However, BC concentrations are generally overestimated by many models in the upper troposphere. With MADE3 in EMAC, we find better agreement of the simulated BC profiles with HIPPO data than the multi-model average of the models that took part in the AeroCom project. There is an interesting difference between the profiles from individual campaigns and more "climatological" datasets. For instance, compared to spatially and temporally localized campaigns, the model simulates a more continuous decline in both total

  7. Morphology of mixed primary and secondary organic particles and the adsorption of spectator organic gases during aerosol formation

    PubMed Central

    Vaden, Timothy D.; Song, Chen; Zaveri, Rahul A.; Imre, Dan; Zelenyuk, Alla

    2010-01-01

    Primary organic aerosol (POA) and associated vapors can play an important role in determining the formation and properties of secondary organic aerosol (SOA). If SOA and POA are miscible, POA will significantly enhance SOA formation and some POA vapor will incorporate into SOA particles. When the two are not miscible, condensation of SOA on POA particles forms particles with complex morphology. In addition, POA vapor can adsorb to the surface of SOA particles increasing their mass and affecting their evaporation rates. To gain insight into SOA/POA interactions we present a detailed experimental investigation of the morphologies of SOA particles formed during ozonolysis of α-pinene in the presence of dioctyl phthalate (DOP) particles, serving as a simplified model of hydrophobic POA, using a single-particle mass spectrometer. Ultraviolet laser depth-profiling experiments were used to characterize two different types of mixed SOA/DOP particles: those formed by condensation of the oxidized α-pinene products on size-selected DOP particles and by condensation of DOP on size-selected α-pinene SOA particles. The results show that the hydrophilic SOA and hydrophobic DOP do not mix but instead form layered phases. In addition, an examination of homogeneously nucleated SOA particles formed in the presence of DOP vapor shows them to have an adsorbed DOP coating layer that is ∼4 nm thick and carries 12% of the particles mass. These results may have implications for SOA formation and behavior in the atmosphere, where numerous organic compounds with various volatilities and different polarities are present. PMID:20194795

  8. Measurements of stratospheric sulfate mixing ratio with a multi filter sampler

    NASA Astrophysics Data System (ADS)

    Gandrud, B. W.; Lazrus, A. L.

    1981-01-01

    A new multi filter sampler (MFS) was used to measure daily profiles of sulfate aerosol in Alaska during the period July 16 through July 19, 1979. During these 4 days, the variability is such that the percent standard deviation of an individual profile from the mean is as high as 23%. The results of these flights are compared with the Project Airstream results from the same time period.

  9. Extinction ratio improvement by pump-modulated four-wave mixing in a dispersion-flattened nonlinear photonic crystal fiber.

    PubMed

    Chow, K K; Shu, C; Lin, Chinlon; Bjarklev, A

    2005-10-31

    We demonstrate extinction ratio improvement by using pump-modulated four-wave mixing in a dispersion-flattened nonlinear photonic crystal fiber. A 6-dB improvement in the extinction ratio of a degraded return-to-zero signal has been achieved. A power penalty improvement of 3 dB at 10(-9) bit-error-rate level is obtained in the 10 Gb/s bit-error-rate measurements.

  10. Mixing ratios of volatile organic compounds (VOCs) in the atmosphere of Karachi, Pakistan

    NASA Astrophysics Data System (ADS)

    Barletta, Barbara; Meinardi, Simone; Simpson, Isobel J.; Khwaja, Haider A.; Blake, Donald R.; Rowland, F. Sherwood

    Mixing ratios of carbon monoxide (CO), methane (CH 4), non-methane hydrocarbons, halocarbons and alkyl nitrates (a total of 72 species) were determined for 78 whole air samples collected during the winter of 1998-1999 in Karachi, Pakistan. This is the first time that volatile organic compound (VOC) levels in Karachi have been extensively characterized. The overall air quality of the urban environment was determined using air samples collected at six locations throughout Karachi. Methane (6.3 ppmv) and ethane (93 ppbv) levels in Karachi were found to be much higher than in other cities that have been studied. The very high CH 4 levels highlight the importance of natural gas leakage in Karachi. The leakage of liquefied petroleum gas contributes to elevated propane and butane levels in Karachi, although the propane and butane burdens were lower than in other cities (e.g., Mexico City, Santiago). High levels of benzene (0.3-19 ppbv) also appear to be of concern in the Karachi urban area. Vehicular emissions were characterized using air samples collected along the busiest thoroughfare of the city (M.A. Jinnah Road). Emissions from vehicular exhaust were found to be the main source of many of the hydrocarbons reported here. Significant levels of isoprene (1.2 ppbv) were detected at the roadside, and vehicular exhaust is estimated to account for about 20% of the isoprene observed in Karachi. 1,2-Dichloroethane, a lead scavenger added to leaded fuel, was also emitted by cars. The photochemical production of ozone (O 3) was calculated for CO and the various VOCs using the Maximum Incremental Reactivity (MIR) scale. Based on the MIR scale, the leading contributors to O 3 production in Karachi are ethene, CO, propene, m-xylene and toluene.

  11. Uncertainty analysis of projections of ozone-depleting substances: mixing ratios, EESC, ODPs, and GWPs

    NASA Astrophysics Data System (ADS)

    Velders, G. J. M.; Daniel, J. S.

    2013-10-01

    The rates at which ozone depleting substances (ODSs) are removed from the atmosphere, that is, their lifetimes, are key factors for determining the rate of ozone layer recovery in the coming decades. We present here a comprehensive uncertainty analysis of future mixing ratios of ODSs, levels of equivalent effective stratospheric chlorine (EESC), ozone depletion potentials, and global warming potentials, using, among other information, the 2013 WCRP/SPARC assessment of lifetimes of ODSs and their uncertainties. The year EESC returns to pre-1980 levels, a metric commonly used to indicate a level of recovery from ODS-induced ozone depletion, is 2048 for mid-latitudes based on the lifetimes from the SPARC assessment, which is about 2 yr later than based on the lifetimes from the WMO assessment of 2011. However, the uncertainty in this return to 1980 levels is much larger than the 2 yr change. The year EESC returns to pre-1980 levels ranges from 2039 to 2064 (95% confidence interval) for mid-latitudes and 2061 to 2105 for the Antarctic spring. The primary contribution to these ranges comes from the uncertainty in the lifetimes. The earlier years of the return estimates are comparable to a hypothetical scenario in which emissions of ODSs cease in 2014. The later end of the range corresponds to a scenario containing an additional emission of about 7 Mt CFC-11-eq in 2015, which is the same as about 2 times the cumulative anthropogenic emissions of all ODSs from 2014 to 2050, or about 12 times the cumulative HCFC emissions from 2014 to 2050.

  12. Lidar measurements of the column CO2 mixing ratio made by NASA Goddard's CO2 Sounder during the NASA ASCENDS 2014 Airborne campaign.

    NASA Astrophysics Data System (ADS)

    Ramanathan, A. K.; Mao, J.; Abshire, J. B.; Kawa, S. R.

    2015-12-01

    Remote sensing measurements of CO2 from space can help improve our understanding of the carbon cycle and help constrain the global carbon budget. However, such measurements need to be sufficiently accurate to detect small (1 ppm) changes in the CO2 mixing ratio (XCO2) against a large background (~ 400 ppm). Satellite measurements of XCO2 using passive spectrometers, such as those from the Japanese GOSAT (Greenhouse gas Observing Satellite) and the NASA OCO-2 (Orbiting Carbon Observatory-2) are limited to daytime sunlit portions of the Earth and are susceptible to biases from clouds and aerosols. For this reason, NASA commissioned the formulation study of ASCENDS a space-based lidar mission. NASA Goddard Space Flight Center's CO2 Sounder lidar is one candidate approach for the ASCENDS mission. The NASA GSFC CO2 Sounder measures the CO2 mixing ratio using a pulsed multi-wavelength integrated path differential absorption (IPDA) approach. The CO2 Sounder has flown in the 2011, 2013 and 2014 ASCENDS airborne campaigns over the continental US, and has produced measurements in close agreement with in situ measurements of the CO2 column. In 2014, the CO2 Sounder upgraded its laser with a precision step-locked diode laser source to improve the lidar wavelength position accuracy. It also improved its optical receiver with a low-noise, high efficiency, HgCdTe avalanche photo diode detector. The combination of these two technologies enabled lidar XCO2 measurements with unprecedented accuracy. In this presentation, we show analysis from the ASCENDS 2014 field campaign, exploring: (1) Horizontal XCO2 gradients measured by the lidar, (2) Comparisons of lidar XCO2 measurements against the Parameterized Chemistry Transport Model (PCTM), and (3) Lidar column water vapor measurements using a HDO absorption line that occurs next to the CO2 absorption line. This can reduce the uncertainty in the dry air column used in XCO2 retrievals.

  13. Diurnal variations of carbonaceous components, major ions, and stable carbon and nitrogen isotope ratios in suburban aerosols from northern vicinity of Beijing

    NASA Astrophysics Data System (ADS)

    He, Nannan; Kawamura, Kimitaka; Kanaya, Yugo; Wang, Zifa

    2015-12-01

    We report diurnal variations of organic carbon (OC), elemental carbon (EC), water-soluble organic carbon (WSOC) and major ions as well as stable carbon and nitrogen isotope ratios (δ13C and δ15N) in ambient aerosols at a suburban site (Mangshan), 40 km north of Beijing, China. We found that aerosol chemical compositions were largely controlled by the air mass transport from Beijing in daytime with southerly winds and by relatively fresh air mass in nighttime from the northern forest areas with northerly winds. Higher concentrations of aerosol mass and total carbon were obtained in daytime. Further, higher OC/EC ratios were recorded in daytime (4.0 ± 1.7) than nighttime (3.2 ± 0.7), suggesting that OC is formed by photochemical oxidation of gaseous precursors in daytime. Contributions of WSOC to OC were slightly higher in daytime (38%) than nighttime (34%), possibly due to secondary formation of WSOC in daytime. We also found higher concentrations of Ca2+ in daytime, which was originated from the construction dust in Beijing area and transported to the sampling site. δ13C ranged from -25.3 to -21.2‰ (ave. -23.5 ± 0.9‰) in daytime and -29.0 to -21.4‰ (-24.0 ± 1.5‰) in nighttime, suggesting that Mangshan aerosols were more influenced by fossil fuel combustion products in daytime and by terrestrial C3 plants in nighttime. This study suggests that daytime air mass delivery from megacity Beijing largely influence the air quality at the receptor site in the north together with photochemical processing of organic aerosols during the atmospheric transport, whereas the Mangshan site is covered with relatively clean air masses at night.

  14. CONVERTING ISOTOPE RATIOS TO DIET COMPOSITION - THE USE OF MIXING MODELS

    EPA Science Inventory

    Investigations of wildlife foraging ecology with stable isotope analysis are increasing. Converting isotope values to proportions of different foods in a consumer's diet requires the use of mixing models. Simple mixing models based on mass balance equations have been used for d...

  15. Lidar observations of long-range transported Saharan dust over Sofia, Bulgaria: a case study of dust mixed with local aerosols

    NASA Astrophysics Data System (ADS)

    Peshev, Zahary Y.; Dreischuh, Tanja N.; Evgenieva, Tsvetina T.; Deleva, Atanaska D.; Tonev, Dimitar; Stoyanov, Dimitar V.

    2016-07-01

    Two-wavelength (1064/532 nm) lidar observations of long-range transported Saharan dust present in the atmosphere over Sofia, Bulgaria, during a 4-day dust intrusion event in winter 2010, are reported. Aged desert aerosols are detected at altitudes up to 4 km above the sea level, within and above the boundary layer as mixed with other aerosols-representing the particular case under consideration. Optical, microphysical, and dynamical properties of dust aerosols are obtained and analyzed. Special attention is paid to retrieving and vertical profiling of dust backscatter-related Ångström exponents (BAEs), as well as to determining their frequency-count distributions. Obtained BAE values in the range 0.3 to 0.6 (±0.2) indicate domination of coarse particles in the near overmicron size range. Reasonability of coarse-mode-dominated dust size composition is substantiated, based on measurement and transportation-history analysis. The performed frequency-count statistics reveals dust BAE distributions asymmetrically extended to multimode distribution shapes, resulting from dust mixing with finer local aerosol fractions. Peculiarities and patterns of the aerosol dynamics at different stages of dust-loading event are revealed and discussed.

  16. Effects of inoculum to substrate ratio, substrate mix ratio and inoculum source on batch co-digestion of grass and pig manure.

    PubMed

    Dechrugsa, Sumeth; Kantachote, Duangporn; Chaiprapat, Sumate

    2013-10-01

    Biochemical methane potential (BMP) assay was conducted at 35 °C to evaluate the effects of inoculum to substrate ratio (ISR) and substrate mix ratio between para-grass and pig manure co-digesting using different inocula. Rubber latex digester (RLD) inoculum showed higher methanogenic activity (41.4 mL CH4/gVS) than pig farm digester (PFD) inoculum (37.3 mL CH4/gVS). However, the maximum methane yields, occurred at the highest para-grass mix ratio (G), were 369.6, 437.6, 465.9 and 442.6 mL CH4/gTSadded for RLD inoculum, versus 332.4, 475.0, 519.5 and 521.9 mL/gTSadded for PFD inoculum at ISR 1, 2, 3, and 4, respectively. HPr, HBu and HVa appeared at higher G, corresponding to substrate's higher biodegradability. Response surface indicated that higher ISR and G had a significantly positive impact on methane yield. It suggested the use of higher ISR, i.e. 3 or 4, for BMP assay of these co-substrates. Dominant species of fermentative bacteria in each inoculum was tested by DGGE.

  17. A thermodynamic model of mixed organic-inorganic aerosols to predict activity coefficients

    NASA Astrophysics Data System (ADS)

    Zuend, A.; Marcolli, C.; Luo, B. P.; Peter, T.

    2008-08-01

    Tropospheric aerosols contain mixtures of inorganic salts, acids, water, and a large variety of organic compounds. Interactions between these substances in liquid mixtures lead to discrepancies from ideal thermodynamic behaviour. By means of activity coefficients, non-ideal behaviour can be taken into account. We present here a thermodynamic model named AIOMFAC (Aerosol Inorganic-Organic Mixtures Functional groups Activity Coefficients) that is able to calculate activity coefficients covering inorganic, organic, and organic-inorganic interactions in aqueous solutions over a wide concentration range. This model is based on the activity coefficient model LIFAC by Yan et al. (1999) that we modified and reparametrised to better describe atmospherically relevant conditions and mixture compositions. Focusing on atmospheric applications we considered H+, Li+, Na+, K+, NH+4, Mg2+, Ca2+, Cl-, Br-, NO-3, HSO-4, and SO2-4 as cations and anions and a wide range of alcohols/polyols composed of the functional groups CHn and OH as organic compounds. With AIOMFAC, the activities of the components within an aqueous electrolyte solution are well represented up to high ionic strength. Most notably, a semi-empirical middle-range parametrisation of direct organic-inorganic interactions in alcohol+water+salt solutions strongly improves the agreement between experimental and modelled activity coefficients. At room temperature, this novel thermodynamic model offers the possibility to compute equilibrium relative humidities, gas/particle partitioning and liquid-liquid phase separations with high accuracy. In further studies, other organic functional groups will be introduced. The model framework is not restricted to specific ions or organic compounds and is therefore also applicable for other research topics.

  18. A thermodynamic model of mixed organic-inorganic aerosols to predict activity coefficients

    NASA Astrophysics Data System (ADS)

    Zuend, A.; Marcolli, C.; Luo, B. P.; Peter, Th.

    2008-03-01

    Tropospheric aerosols contain mixtures of inorganic salts, acids, water, and a large variety of organic compounds. Interactions between these substances in liquid mixtures lead to discrepancies from ideal thermodynamic behaviour. By means of activity coefficients, non-ideal behaviour can be taken into account. We present here a thermodynamic model named AIOMFAC (Aerosol Inorganic-Organic Mixtures Functional groups Activity Coefficients) that is able to calculate activity coefficients covering inorganic, organic, and organic-inorganic interactions in aqueous solutions over a wide concentration range. This model is based on the activity coefficient model LIFAC by Yan et al. (1999) that we modified and reparametrised to better describe atmospherically relevant conditions and mixture compositions. Focusing on atmospheric applications we considered H+, Li+, Na+, K+, NH4+, Mg2+, Ca2+, Cl-, Br-, NO3-, HSO4-, and SO42- as cations and anions and a wide range of alcohols/polyols composed of the functional groups CHn and OH as organic compounds. With AIOMFAC, the activities of the components within an aqueous electrolyte solution are well represented up to high ionic strength. Most notably, a semi-empirical middle-range parametrisation of direct organic-inorganic interactions in alcohol + water + salt solutions strongly improves the agreement between experimental and modelled activity coefficients. At room temperature, this novel thermodynamic model offers the possibility to compute equilibrium relative humidities, gas/particle partitioning and liquid-liquid phase separations with high accuracy. In further studies, other organic functional groups will be introduced. The model framework is not restricted to specific ions or organic compounds and is therefore also applicable for other research topics.

  19. Uncertainty analysis of projections of ozone-depleting substances: mixing ratios, EESC, ODPs, and GWPs

    NASA Astrophysics Data System (ADS)

    Velders, G. J. M.; Daniel, J. S.

    2014-03-01

    The rates at which ozone-depleting substances (ODSs) are removed from the atmosphere, which determine the lifetimes of these ODSs, are key factors for determining the rate of ozone layer recovery in the coming decades. We present here a comprehensive uncertainty analysis of future mixing ratios of ODSs, levels of equivalent effective stratospheric chlorine (EESC), ozone depletion potentials, and global warming potentials (GWPs), using, among other information, the 2013 WCRP/SPARC (World Climate Research Programme/Stratospheric Processes and their Role in Climate) assessment of lifetimes of ODSs and their uncertainties. The year EESC returns to pre-1980 levels, a metric commonly used to indicate a level of recovery from ODS-induced ozone depletion, is 2048 for midlatitudes and 2075 for Antarctic conditions based on the lifetimes from the SPARC assessment, which is about 2 and 4 yr, respectively, later than based on the lifetimes from the WMO (World Meteorological Organization) assessment of 2011. However, the uncertainty in this return to 1980 levels is much larger than the shift due to this change in lifetimes. The year EESC returns to pre-1980 levels ranges from 2039 to 2064 (95% confidence interval) for midlatitudes and from 2061 to 2105 for the Antarctic spring. The primary contribution to these ranges comes from the uncertainty in the lifetimes, with smaller contributions from uncertainties in other modeled parameters. The earlier years of the return estimates derived by the uncertainty analysis, i.e., 2039 for midlatitudes and 2061 for Antarctic spring, are comparable to a hypothetical scenario in which emissions of ODSs cease in 2014. The later end of the range, i.e., 2064 for midlatitudes and 2105 for Antarctic spring, can also be obtained by a scenario with an additional emission of about 7 Mt CFC-11 eq. (eq. - equivalent) in 2015, which is the same as about 2 times the projected cumulative anthropogenic emissions of all ODSs from 2014 to 2050, or about 12

  20. Uncertainty Analysis of Ozone-Depleting Substances: Mixing Ratios, EESC, ODPs, and GWPs

    NASA Astrophysics Data System (ADS)

    Velders, G. J.; Daniel, J. S.

    2013-12-01

    Important for the recovery of the ozone layer from depletion by ozone-depleting substances (ODSs) is the rate at which ODSs are removed from the atmosphere, that is, their lifetimes. Recently the WCRP/SPARC project conducted an assessment of lifetimes of ODSs [SPARC, 2013] and presented a new set of recommended lifetimes as well as their uncertainties. We present here a comprehensive uncertainty analysis of ODS mixing ratios, levels of equivalent effective stratospheric chlorine (EESC), radiative forcing, ozone depletion potentials (ODPs), and global warming potentials (GWPs), using the new lifetimes and their uncertainties as well as uncertainties on all other relevant parameters. Using a box model the year EESC returns to pre-1980 levels, a metric commonly used to indicate a level of recovery for ODS induced ozone depletion, is 2048 for mid-latitudes based on the new lifetimes, which is 2 years later than that based on the lifetimes from WMO [2011]. The uncertainty in this return time is much larger than this change, however. The year EESC returns to pre-1980 levels ranges from is 2038 to 2064 (95% CI) for mid-latitudes and 2060 to 2104 for the Antarctic. The largest contribution to these ranges comes from the uncertainties in the lifetimes, since the current atmospheric burden of CFCs is much larger than the amounts present in existing equipment or still being produced. The earlier end of the recovery times is comparable to the return time in a hypothetical scenario with a cease in anthropogenic ODS emissions in 2014. The upper end of the range corresponds with an extra emission of about 7 MtCFC-11-eq in 2015, or about twice the cumulative anthropogenic emissions of all ODSs from 2014 to 2050. Semi-empirical ODPs calculated using the lifetimes from SPARC [2013] are up to 25% lower than the data reported in WMO [2011] for most species, mainly as a result of the increase in the estimated lifetime of CFC-11. The ODP of Halon-2402 increases by 20%, while the only

  1. Validating MODIS above-cloud aerosol optical depth retrieved from "color ratio" algorithm using direct measurements made by NASA's airborne AATS and 4STAR sensors

    NASA Astrophysics Data System (ADS)

    Jethva, Hiren; Torres, Omar; Remer, Lorraine; Redemann, Jens; Livingston, John; Dunagan, Stephen; Shinozuka, Yohei; Kacenelenbogen, Meloe; Segal Rosenheimer, Michal; Spurr, Rob

    2016-10-01

    We present the validation analysis of above-cloud aerosol optical depth (ACAOD) retrieved from the "color ratio" method applied to MODIS cloudy-sky reflectance measurements using the limited direct measurements made by NASA's airborne Ames Airborne Tracking Sunphotometer (AATS) and Spectrometer for Sky-Scanning, Sun-Tracking Atmospheric Research (4STAR) sensors. A thorough search of the airborne database collection revealed a total of five significant events in which an airborne sun photometer, coincident with the MODIS overpass, observed partially absorbing aerosols emitted from agricultural biomass burning, dust, and wildfires over a low-level cloud deck during SAFARI-2000, ACE-ASIA 2001, and SEAC4RS 2013 campaigns, respectively. The co-located satellite-airborne matchups revealed a good agreement (root-mean-square difference < 0.1), with most matchups falling within the estimated uncertainties associated the MODIS retrievals (about -10 to +50 %). The co-retrieved cloud optical depth was comparable to that of the MODIS operational cloud product for ACE-ASIA and SEAC4RS, however, higher by 30-50 % for the SAFARI-2000 case study. The reason for this discrepancy could be attributed to the distinct aerosol optical properties encountered during respective campaigns. A brief discussion on the sources of uncertainty in the satellite-based ACAOD retrieval and co-location procedure is presented. Field experiments dedicated to making direct measurements of aerosols above cloud are needed for the extensive validation of satellite-based retrievals.

  2. Complex vertical layering and mixing of aerosols over the eastern Mediterranean: active and passive remote sensing at the Cyprus University of Technology

    NASA Astrophysics Data System (ADS)

    Mamouri, R.-E.; Nisantzi, A.; Hadjimitsis, D. G.; Ansmann, A.; Schwarz, A.; Basart, S.; Baldasano, J. M.

    2013-08-01

    Aerosols can have a complicated influence on climate conditions, directly as well as indirectly via cloud formation. The southeastern Mediterranean region can be characterized as a cross road of aerosols originating from European, Asian and African continents. Complex vertical aerosol distributions are frequently detected over Cyprus by means of active remote sensing. Observations of such complex aerosol layering and comparison of the measurements with aerosol products of regional and global atmospheric transport models are required to improve our understanding of life cycles of aerosol mixtures and their impact on climate as well as on satellite remote sensing products. In this study, a case of an intense desert dust outbreak from Syria and Saudi Arabia towards the eastern Mediterranean in September 2011 is presented. The observations used in this study were performed with a 532-nm polarization Lidar and a sun/sky AERONET photometer operated at 8 channels from 340 to 1640 nm wavelength. Both instruments belong to remote sensing station of the Cyprus Technical University at Limassol, Cyprus (34°N, 33°E). The lofted dust plume was doped with air masses that crossed sources of biomass burning smoke and anthropogenic pollution. In addition, the shallow marine boundary layer over the Mediterranean Sea and over Limassol became mixed with the anthropogenic haze by sea breeze circulations. The case study demonstrates the potential of combined lidar/photometer observations to deliver detailed vertically resolved information of the aerosol characteristics in terms of particle optical and microphysical properties, separately for the spherical particle fraction as well as for the non-spherical aerosol mode.

  3. 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.

  4. Reactive bromine chemistry in Mt. Etna's volcanic plume: the influence of total Br, high temperature processing, aerosol loading and plume-air mixing

    NASA Astrophysics Data System (ADS)

    Roberts, T. J.; Martin, R. S.; Jourdain, L.

    2014-03-01

    Volcanic emissions present a source of reactive halogens to the troposphere, through rapid plume chemistry that converts the emitted HBr to more reactive forms such as BrO. The nature of this process is poorly quantified, yet is of interest to understand volcanic impacts on the troposphere, and infer volcanic activity from volcanic gas measurements (i.e. BrO / SO2 ratios). Recent observations from Etna report an initial increase and subsequent plateau or decline in BrO / SO2 ratios with distance downwind. We present daytime PlumeChem model simulations that reproduce and explain the reported trend in BrO / SO2 at Etna including the initial rise and subsequent plateau. Through suites of model simulations we also investigate the influences of volcanic aerosol loading, bromine emission, and plume-air mixing rate on the downwind plume chemistry. Emitted volcanic HBr is converted into reactive bromine by autocatalytic bromine chemistry cycles whose onset is accelerated by the model high-temperature initialisation. These rapid chemistry cycles also impact the reactive bromine speciation through inter-conversion of Br, Br2, BrO, BrONO2, BrCl, HOBr. Formation of BrNO2 is also discussed. We predict a new evolution of Br-speciation in the plume, with BrO, Br2, Br and HBr as the main plume species in the near downwind plume whilst BrO, and HOBr are present in significant quantities further downwind (where BrONO2 and BrCl also make up a minor fraction). The initial rise in BrO / SO2 occurs as ozone is entrained into the plume whose reaction with Br promotes net formation of BrO. Aerosol has a modest impact on BrO / SO2 near-downwind (< 6 km) at the relatively high loadings considered. The subsequent decline in BrO / SO2 occurs as entrainment of oxidants HO2 and NO2 promotes net formation of HOBr and BrONO2, whilst the plume dispersion dilutes volcanic aerosol so slows the heterogeneous loss rates of these species. A higher volcanic aerosol loading enhances BrO / SO2 in the (> 6

  5. Characterization of submicron particles influenced by mixed biogenic and anthropogenic emissions using high-resolution aerosol mass spectrometry: results from CARES

    SciTech Connect

    Setyan, Ari; Zhang, Qi; Merkel, M.; Knighton, Walter B.; Sun, Y.; Song, Chen; Shilling, John E.; Onasch, Timothy B.; Herndon, Scott C.; Worsnop, Douglas R.; Fast, Jerome D.; Zaveri, Rahul A.; Berg, Larry K.; Wiedensohler, A.; Flowers, B. A.; Dubey, Manvendra K.; Subramanian, R.

    2012-09-11

    The Carbonaceous Aerosols and Radiative Effects Study (CARES) took place in the Sacramento Valley of California in summer 2010. We present results obtained at Cool, CA, the T1 site of the project ({approx}40 km downwind of urban emissions from Sacramento), where we deployed an Aerodyne high resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS) in parallel with complementary instrumentation to characterize the sources and processes of submicron particles (PM1). Cool is located at the foothill of the Sierra Nevada Mountains, where intense biogenic emissions are periodically mixed with urban outflow transported by daytime southwesterly winds from the Sacramento metropolitan area. The particle mass loading was low (3.0 {micro}gm{sup -3} on average) and dominated by organics (80% of the PM1 mass) followed by sulfate (9.9 %). Organics and sulfate appeared to be externally mixed, as suggested by their different time series (r2 = 0.13) and size distributions. Sulfate showed a bimodal distribution with a droplet mode peaking at {approx}400nm in vacuum aerodynamic diameter (Dva), and a condensation mode at {approx}150 nm, while organics generally displayed a broad distribution in 60-600nm (Dva). New particle formation and growth events were observed almost every day, emphasizing the roles of organics and sulfate in new particle growth, especially that of organics. The organic aerosol (OA) had a nominal formula of C{sub 1}H{sub 1.38}N{sub 0.004}O{sub 0.44}, thus an average organic mass-to-carbon (OM/OC) ratio of 1.70. Two different oxygenated OA (OOA, 90% of total OA mass) and a hydrocarbon-like OA (HOA, 10 %) were identified by Positive matrix factorization (PMF) of the high resolution mass spectra. The more oxidized MO-OOA (O/C = 0.54) corresponded to secondary OA (SOA) primarily influenced by biogenic emissions, while the less oxidized LO-OOA (O/C = 0.42) corresponded to SOA associated with urban transport. The HOA factor corresponded to primary emissions mainly

  6. Optics of Water Cloud Droplets Mixed with Black-Carbon Aerosols

    NASA Technical Reports Server (NTRS)

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

    2014-01-01

    We use the recently extended superposition T-matrix method to calculate scattering and absorption properties of micrometer-sized water droplets contaminated by black carbon. Our numerically exact results reveal that, depending on the mode of soot-water mixing, the soot specific absorption can vary by a factor exceeding 6.5. The specific absorption is maximized when the soot material is quasi-uniformly distributed throughout the droplet interior in the form of numerous small monomers. The range of mixing scenarios captured by our computations implies a wide range of remote sensing and radiation budget implications of the presence of black carbon in liquid-water clouds. We show that the popular Maxwell-Garnett effective-medium approximation can be used to calculate the optical cross sections, single-scattering albedo, and asymmetry parameter for the quasi-uniform mixing scenario, but is likely to fail in application to other mixing scenarios and in computations of the elements of the scattering matrix.

  7. Mixing a sol and a precipitate of block copolymers with different block ratios leads to an injectable hydrogel.

    PubMed

    Yu, Lin; Zhang, Zheng; Zhang, Huan; Ding, Jiandong

    2009-06-08

    A facile method to obtain a thermoreversible physical hydrogel was found by simply mixing an aqueous sol of a block copolymer with a precipitate of a similar copolymer but with a different block ratio. Two ABA-type triblock copolymers poly(D,L-lactic acid-co-glycolic acid)-B-poly(ethylene glycol)-B-poly(D,L-lactic acid-co-glycolic acid) (PLGA-PEG-PLGA) were synthesized. One sample in water was a sol in a broad temperature region, while the other in water was just a precipitate. The mixture of these two samples with a certain mix ratio underwent, however, a sol-to-gel-to-precipitate transition upon an increase of temperature. A dramatic tuning of the sol-gel transition temperature was conveniently achieved by merely varying mix ratio, even in the case of a similar molecular weight. Our study indicates that the balance of hydrophobicity and hydrophilicity within this sort of amphiphilic copolymers is critical to the inverse thermal gelation in water resulting from aggregation of micelles. The availability of encapsulation and sustained release of lysozyme, a model protein by the thermogelling systems was confirmed. This "mix" method provides a very convenient approach to design injectable thermogelling biomaterials with a broad adjustable window, and the novel copolymer mixture platform is potentially used in drug delivery and other biomedical applications.

  8. Fifteen years of atmospheric methane and carbon dioxide mixing ratio measurements at the mountain site Kasprowy Wierch, southern Poland

    NASA Astrophysics Data System (ADS)

    Chmura, L.; Korus, A.; Necki, J.; Rozanski, K.; Zimnoch, M.

    2009-04-01

    The Kasprowy Wierch station is located in the south of Poland, within the High Tatra Mountains. The meteorological observatory which hosts the monitoring station is located on top of a mountain peak called Kasprowy Wierch (49o14'N, 19o59'E, 1989 m a.s.l., 300 m above the tree line). Climate of Kasprowy Wierch area is typical for a continental mountain location, with relatively large diurnal and seasonal variations of temperature, high precipitation rate, frequent changes of atmospheric pressure and strong winds. Regular observations of atmospheric CH4 and CO2mixing ratios at Kasprowy Wierch begun in 1994. Continuous measurements using GC technique were initiated in 1996. The available dataset of CO2 and CH4mixing ratios at Kasprowy Wierch comprise a valuable source of information about temporal variability of those gases in the atmosphere above central Europe over 15-year period. Significant year-to-year variability of carbon dioxide mixing ratio, both with respect to the observed annual growth rate as well as the amplitude of seasonal changes, was observed. The presented carbon dioxide mixing ratio record reveals typical behaviour of atmospheric CO2 observed at mid-latitude continental sites of the Northern Hemisphere. The winter maximum ends in spring, when the photosynthetic sink starts to operate. From that time on, the CO2 mixing ratio gradually decreases, reaching a minimum in August/September. Afterwards, the CO2 level increases, reaching winter maximum in February/March. The length of the CO2 deficit season at Kasprowy Wierch, defined as the period when CO2 mixing ratio remains below the long-term trend curve, is getting shorter (c.a. -0.5 ppm year-1, averaged over the observation period 1994-2008). The average peak-to-peak amplitude for the period 1994-2008 is equal c.a. 19 ppm (minimum value of 14,7 ppm recorded in 2003 and maximum of 20,7 ppm recorded in 1995). It is worth to note that the 2003 summer draw-down of CO2 concentration at Kasprowy Wierch was

  9. Influence of mixed liquor recycle ratio and dissolved oxygen on performance of pre-denitrification submerged membrane bioreactors.

    PubMed

    Tan, Teck Wee; Ng, How Yong

    2008-02-01

    The conflicting influence of mixed liquor recycle ratio and dissolved oxygen on nitrogen removal and membrane fouling of a pre-denitrification submerged MBR was investigated in this study. It was found that a high aeration rate of 10 L air/min was able to minimize membrane fouling as compared with lower aeration rates of 5 and 2.5L air/min in this study. Faster fouling at lower aeration rate was due to the decrease in cross-flow velocity across the membrane surface. However, high DO concentration (average of 5.1+/-0.5mg O2/L) present in the recycle mixed liquor at an aeration rate of 10 L air/min deteriorated the TN removal efficiency when operating at a recycle ratio of more than 3. A lower aeration rate of 5L air/min, resulting in an average DO concentration of 3.4+/-0.7 mg O2/L in the recycle mixed liquor, led to an improvement in TN removal efficiency: 63%, 80%, 84% and 89% for mixed liquor recycle ratio of 1, 3, 5 and 10, respectively. Further decrease in aeration rate to 2.5L air/min, resulting in an average DO concentration of 1.9+/-0.8 mg O2/L, did not improve the TN removal efficiency. Using a newly developed simplified nitrification-denitrification model, it was calculated that the COD/NO3(-)-N required for denitrification at 10 L air/min aeration rate was higher than those associated with 5 and 2.5L air/min aeration rates. The model also revealed that denitrification at an aeration rate of 10 L air/min was limited by COD concentration present in the wastewater when operating at a mixed liquor recycle ratio of 3 and higher.

  10. Arctic organic aerosol measurements show particles from mixed combustion in spring haze and from frost flowers in winter

    NASA Astrophysics Data System (ADS)

    Shaw, P. M.; Russell, L. M.; Jefferson, A.; Quinn, P. K.

    2010-05-01

    Submicron atmospheric aerosol particles were collected between 1 March 2008 and 1 March 2009 at Barrow, Alaska, to characterize the organic mass (OM) in the Arctic aerosol. Organic functional group concentrations and trace metals were measured with FTIR on submicron particles collected on Teflon filters. The OM varied from 0.07 μg m-3 in summer to 0.43 μg m-3 in winter, and 0.35 μg m-3 in spring, showing a transition in OM composition between spring and winter. Most of the OM in spring could be attributed to anthropogenic sources, consisting primarily of alkane and carboxylic acid functional groups and correlated to elemental tracers of industrial pollution, biomass burning, and shipping emissions. PMF analysis associated OM with two factors, a Mixed Combustion factor (MCF) and an Ocean-derived factor (ODF). Back trajectory analysis revealed that the highest fractions of the MCF were associated with air masses that had originated from northeastern Asia and the shipping lanes south of the Bering Straits. The ODF consisted of organic hydroxyl groups and correlated with organic and inorganic seawater components. The ODF accounted for more than 55% of OM in winter when the sampled air masses originated along the coastal and lake regions of the Northwest Territories of Canada. Frost flowers with organic-salt coatings that arise by brine rejection during sea ice formation may account for this large source of carbohydrate-like OM during the ice-covered winter season. While the anthropogenic sources contributed more than 0.3 μg m-3 of the springtime haze OM, ocean-derived particles provided comparable OM sources in winter.

  11. Late-occurring pulmonary pathologies following inhalation of mixed oxide (uranium + plutonium oxide) aerosol in the rat.

    PubMed

    Griffiths, N M; Van der Meeren, A; Fritsch, P; Abram, M-C; Bernaudin, J-F; Poncy, J L

    2010-09-01

    Accidental exposure by inhalation to alpha-emitting particles from mixed oxide (MOX: uranium and plutonium oxide) fuels is a potential long-term health risk to workers in nuclear fuel fabrication plants. For MOX fuels, the risk of lung cancer development may be different from that assigned to individual components (plutonium, uranium) given different physico-chemical characteristics. The objective of this study was to investigate late effects in rat lungs following inhalation of MOX aerosols of similar particle size containing 2.5 or 7.1% plutonium. Conscious rats were exposed to MOX aerosols and kept for their entire lifespan. Different initial lung burdens (ILBs) were obtained using different amounts of MOX. Lung total alpha activity was determined by external counting and at autopsy for total lung dose calculation. Fixed lung tissue was used for anatomopathological, autoradiographical, and immunohistochemical analyses. Inhalation of MOX at ILBs ranging from 1-20 kBq resulted in lung pathologies (90% of rats) including fibrosis (70%) and malignant lung tumors (45%). High ILBs (4-20 kBq) resulted in reduced survival time (N = 102; p < 0.05) frequently associated with lung fibrosis. Malignant tumor incidence increased linearly with dose (up to 60 Gy) with a risk of 1-1.6% Gy for MOX, similar to results for industrial plutonium oxide alone (1.9% Gy). Staining with antibodies against Surfactant Protein-C, Thyroid Transcription Factor-1, or Oct-4 showed differential labeling of tumor types. In conclusion, late effects following MOX inhalation result in similar risk for development of lung tumors as compared with industrial plutonium oxide.

  12. Effects of turbulence on mixed-phase deep convective clouds under different basic-state winds and aerosol concentrations

    NASA Astrophysics Data System (ADS)

    Lee, Hyunho; Baik, Jong-Jin; Han, Ji-Young

    2014-12-01

    The effects of turbulence-induced collision enhancement (TICE) on mixed-phase deep convective clouds are numerically investigated using a 2-D cloud model with bin microphysics for uniform and sheared basic-state wind profiles and different aerosol concentrations. Graupel particles account for the most of the cloud mass in all simulation cases. In the uniform basic-state wind cases, graupel particles with moderate sizes account for some of the total graupel mass in the cases with TICE, whereas graupel particles with large sizes account for almost all the total graupel mass in the cases without TICE. This is because the growth of ice crystals into small graupel particles is enhanced due to TICE. The changes in the size distributions of graupel particles due to TICE result in a decrease in the mass-averaged mean terminal velocity of graupel particles. Therefore, the downward flux of graupel mass, and thus the melting of graupel particles, is reduced due to TICE, leading to a decrease in the amount of surface precipitation. Moreover, under the low aerosol concentration, TICE increases the sublimation of ice particles, consequently playing a partial role in reducing the amount of surface precipitation. The effects of TICE are less pronounced in the sheared basic-state wind cases than in the uniform basic-state wind cases because the number of ice crystals is much smaller in the sheared basic-state wind cases than in the uniform basic-state wind cases. Thus, the size distributions of graupel particles in the cases with and without TICE show little difference.

  13. The retrieval of atmospheric constituent mixing-ratio profiles from solar absorption spectra. Ph.D. Thesis. Interim Technical Report

    NASA Technical Reports Server (NTRS)

    Shaffer, W. A.

    1983-01-01

    Methods used to determine various atmospheric gas distributions are summarized. The experimentally determined mixing ratio profiles (the mixing ratio of a gas is the ratio of the number of gas molecules to the number of air molecules) of some atmospheric gases are shown. In most in situ experiments stratospheric gas samples are collected at several altitudes by balloon, aircraft, or rocket. These samples are then analyzed by various methods. Mixing ratio profiles of Ci, ClO, and OH were determined by laser induced fluorescence of samples. Others have analyzed gas samples by gas chromatography in order to determine the molecular abundances of CCl2F2, CCl4, CCl3F, CFCl3, CF2Cl2, CHClF2, CH3CCl3, CH4, CO, C2Cl3F3, C2Cl4, C2HCl3, C2H2, C2H4, C2H6, C3H8, C6H6, C7H8, H2, and N2O.

  14. Observations of Atmospheric Methane and Carbon Dioxide Mixing Ratios: Tall-Tower or Mountain-Top Stations?

    NASA Astrophysics Data System (ADS)

    Bamberger, Ines; Oney, Brian; Brunner, Dominik; Henne, Stephan; Leuenberger, Markus; Buchmann, Nina; Eugster, Werner

    2017-02-01

    Mountain-top observations of greenhouse gas mixing ratios may be an alternative to tall-tower measurements for regional scale source and sink estimation. To investigate the equivalence or limitations of a mountain-top site as compared to a tall-tower site, we used the unique opportunity of comparing in situ measurements of methane (CH4 ) and carbon dioxide (CO2 ) mixing ratios at a mountain top (986 m above sea level, a.s.l.) with measurements from a nearby (distance 28.4 km) tall tower, sampled at almost the same elevation (1009 m a.s.l.). Special attention was given to, (i) how local wind statistics and greenhouse gas sources and sinks at the mountain top influence the observations, and (ii) whether mountain-top observations can be used as for those from a tall tower for constraining regional greenhouse gas emissions. Wind statistics at the mountain-top site are clearly more influenced by local flow systems than those at the tall-tower site. Differences in temporal patterns of the greenhouse gas mixing ratios observed at the two sites are mostly related to the influence of local sources and sinks at the mountain-top site. Major influences of local sources can be removed by applying a statistical filter (5{th} percentile) or a filter that removes periods with unfavourable flow conditions. In the best case, the bias in mixing ratios between the mountain-top and the tall-tower sites after the application of the wind filter was {-}0.0005± 0.0010 ppm for methane (September, 0000-0400 UTC) and 0.11± 0.18 ppm for CO2 (February, 1200-1600 UTC). Temporal fluctuations of atmospheric CH4 and CO2 mixing ratios at both stations also showed good agreement (apart from CO2 during summertime) as determined by moving bi-weekly Pearson correlation coefficients (up to 0.96 for CO2 and 0.97 for CH4 ). When only comparing mixing ratios minimally influenced by local sources (low bias and high correlation coefficients), our measurements indicate that mountain-top observations are

  15. Water Vapour Mixing Ratio Measurements in Potenza in the Frame of the International Network for the Detection of Atmospheric Composition Change - NDACC

    NASA Astrophysics Data System (ADS)

    De Rosa, Benedetto; Di Girolamo, Paolo; Summa, Donato; Stelitano, Dario; Mancini, Ignazio

    2016-06-01

    In November 2012 the University of BASILicata Raman Lidar system (BASIL) was approved to enter the International Network for the Detection of Atmospheric Composition Change (NDACC). This network includes more than 70 high-quality, remote-sensing research stations for observing and understanding the physical and chemical state of the upper troposphere and stratosphere and for assessing the impact of stratosphere changes on the underlying troposphere and on global climate. As part of this network, more than thirty groundbased Lidars deployed worldwide are routinely operated to monitor atmospheric ozone, temperature, aerosols, water vapour, and polar stratospheric clouds. In the frame of NDACC, BASIL performs measurements on a routine basis each Thursday, typically from local noon to midnight, covering a large portion of the daily cycle. Measurements from BASIL are included in the NDACC database both in terms of water vapour mixing ratio and temperature. This paper illustrates some measurement examples from BASIL, with a specific focus on water vapour measurements, with the goal to try and characterize the system performances.

  16. Atmospheric trace metals over the Atlantic and South Indian Oceans: Investigation of metal concentrations and lead isotope ratios in coastal and remote marine aerosols

    NASA Astrophysics Data System (ADS)

    Witt, Melanie; Baker, Alex R.; Jickells, Tim D.

    Atmospheric concentrations of trace metals over the oceans are investigated through analysis of aerosol samples collected during cruises from the UK to the Falkland Islands and from South Africa to Australia. The readily soluble concentrations of Cu (4-256 pmol m -3), Ni (0.1-54 pmol m -3), Ba (0.2-60 pmol m -3), Zn (6-316 pmol m -3), Cd (0.01-0.29 pmol m -3) and Pb (0.4-22 pmol m -3) were measured in the aerosols, along with total concentrations of crustal elements (Fe, Al and Mn) to evaluate the crustal contributions. Air mass back trajectories suggested most of the aerosol samples had spent several days over the ocean prior to collection. The highest metal concentrations were observed in aerosols close to South Africa, Australia and major cities in South America, although these concentrations were lower than had been reported previously in the literature. Apart from Ba, which had a major crustal source, the trace metals were enriched relative to crustal sources in most samples, including some collected thousands of kilometers from emission sources. The mean trace metal concentrations in the remote Indian Ocean were lower than those measured in the Atlantic Ocean. Even lower concentrations are reported in the literature for the remote Pacific Ocean. In contrast to previous studies, no clear north-south gradient is observed in the concentrations of the trace metals in the aerosols. Lead isotope measurements were also carried out on aerosol samples using a multicollector inductively coupled plasma mass spectrometer to assist in source apportionment. Clear differences were noted in the isotope ratios collected on either side of the Indian Ocean with Australian lead ore dominating over much of the eastern and mid-southern Indian Ocean. Samples collected over the western Indian Ocean and Atlantic Ocean under South African influence had lead isotopes quite different from those seen in South African cities in the past, and are closer in ratio to the coal signature of

  17. Atmospheric carbon diooxide mixing ratios from the NOAA Climate Monitoring and Diagnostics Laboratory cooperative flask sampling network, 1967-1993

    SciTech Connect

    Conway, T.J.; Tans, P.P.; BBoden, T.A.

    1996-02-01

    This data report documents monthly atmospheric CO{sub 2} mixing ratios and measurements obtained by analyzing individual flask air samples for the NOAA/CMDL global cooperative flask sampling network. Measurements include land-based sampling sites and shipboard measurements covering 14 latitude bands in the Pacific Ocean and South China Sea. Analysis of the NOAA/CMDL flask CO{sub 2} database shows a long-term increase in atmospheric CO{sub 2} mixing ratios since the late 1960s. This report describes how the samples are collected and analyzed and how the data are processed, defines limitations, and restrictions of the data, describes the contents and format of the data files, and provides tabular listings of the monthly carbon dioxide records.

  18. The Impact of New Estimates of Mixing Ratio and Flux-based Halogen Scenarios on Ozone Evolution

    NASA Technical Reports Server (NTRS)

    Oman, Luke D.; Douglass, Anne R.; Liang, Qing; Strahan, Susan E.

    2014-01-01

    The evolution of ozone in the 21st century has been shown to be mainly impacted by the halogen emissions scenario and predicted changes in the circulation of the stratosphere. New estimates of mixing ratio and flux-based emission scenarios have been produced from the SPARC Lifetime Assessment 2013. Simulations using the Goddard Earth Observing System Chemistry-Climate Model (GEOSCCM) are conducted using this new A1 2014 halogen scenario and compared to ones using the A1 2010 scenario. This updated version of GEOSCCM includes a realistic representation of the Quasi-Biennial Oscillation and improvements related to the break up of the Antarctic polar vortex. We will present results of the ozone evolution over the recent past and 21st century to the A1 2010, A1 2014 mixing ratio, and an A1 2014 flux-based halogen scenario. Implications of the uncertainties in these estimates as well as those from possible circulation changes will be discussed.

  19. Methods for Retrievals of CO2 Mixing Ratios from JPL Laser Absorption Spectrometer Flights During a Summer 2011 Campaign

    NASA Technical Reports Server (NTRS)

    Menzies, Robert T.; Spiers, Gary D.; Jacob, Joseph C.

    2013-01-01

    The JPL airborne Laser Absorption Spectrometer instrument has been flown several times in the 2007-2011 time frame for the purpose of measuring CO2 mixing ratios in the lower atmosphere. This instrument employs CW laser transmitters and coherent detection receivers in the 2.05- micro m spectral region. The Integrated Path Differential Absorption (IPDA) method is used to retrieve weighted CO2 column mixing ratios. We present key features of the evolving LAS signal processing and data analysis algorithms and the calibration/validation methodology. Results from 2011 flights in various U.S. locations include observed mid-day CO2 drawdown in the Midwest and high spatial resolution plume detection during a leg downwind of the Four Corners power plant in New Mexico.

  20. Airborne Laser Absorption Spectrometer Measurements of CO2 Column Mixing Ratios: Source and Sink Detection in the Atmospheric Environment

    NASA Astrophysics Data System (ADS)

    Menzies, Robert T.; Spiers, Gary D.; Jacob, Joseph C.

    2016-06-01

    The JPL airborne Laser Absorption Spectrometer instrument has been flown several times in the 2007-2011 time frame for the purpose of measuring CO2 mixing ratios in the lower atmosphere. The four most recent flight campaigns were on the NASA DC-8 research aircraft, in support of the NASA ASCENDS (Active Sensing of CO2 Emissions over Nights, Days, and Seasons) mission formulation studies. This instrument operates in the 2.05-μm spectral region. The Integrated Path Differential Absorption (IPDA) method is used to retrieve weighted CO2 column mixing ratios. We present key features of the CO2LAS signal processing, data analysis, and the calibration/validation methodology. Results from flights in various U.S. locations during the past three years include observed mid-day CO2 drawdown in the Midwest, also cases of point-source and regional plume detection that enable the calculation of emission rates.

  1. Variations in methane and nitrous oxide mixing ratios at the southern boundary of a Canadian boreal forest

    NASA Astrophysics Data System (ADS)

    Simpson, I. J.; Edwards, G. C.; Thurtell, G. W.

    Diurnal and seasonal variations in methane (CH 4) and nitrous oxide (N 2O) mixing ratios were measured above a boreal aspen stand at the southern boundary of the Canadian boreal forest, about 5 km north of agricultural land. The research was conducted between 16 April and 16 September 1994, in the Prince Albert National Park, Saskatchewan, to better understand patterns of CH 4 and N 2O cycling in boreal ecosystems. The research also presents a method for detecting the long-range transport of trace gases using a micrometeorological, laser-based gas monitoring system. Both CH 4 and N 2O featured diurnal cycles consistent with a pattern of net emission for each trace gas. The CH 4 mixing ratio displayed a seasonal variation that was strongly related to soil temperature, with measured values roughly 30 ppb higher in the late summer than in spring. During the latter half of the experiment, the CH 4 mixing ratios varied with wind direction and suggested areas of higher emission to the northeast and east of the measurement tower. The N 2O fluxes also showed favoured directions, although in this case the highest mixing ratios were measured during the springtime in air masses originating south and southwest of the tower. The high springtime values coincided with spring thaw emissions of N 2O from agricultural fields to the south, and the results suggest that the trace gas analysis system detected the long-range transport of N 2O from the agricultural land. Ammonia and ammonium likewise may be transported to the southern boreal forest from agricultural land, and a future investigation at this site could seek to determine the effect of their long-range transport on the southern boreal forest.

  2. Converting isotope ratios to diet composition - the use of mixing models - June 2010

    EPA Science Inventory

    One application of stable isotope analysis is to reconstruct diet composition based on isotopic mass balance. The isotopic value of a consumer’s tissue reflects the isotopic values of its food sources proportional to their dietary contributions. Isotopic mixing models are used ...

  3. Simulation of the effects of aerosol on mixed-phase orographic clouds using the WRF model with a detailed bin microphysics scheme

    NASA Astrophysics Data System (ADS)

    Xiao, Hui; Yin, Yan; Jin, Lianji; Chen, Qian; Chen, Jinghua

    2015-08-01

    The Weather Research Forecast (WRF) mesoscale model coupled with a detailed bin microphysics scheme is used to investigate the impact of aerosol particles serving as cloud condensation nuclei and ice nuclei on orographic clouds and precipitation. A mixed-phase orographic cloud developed under two scenarios of aerosol (a typical continental background and a relatively polluted urban condition) and ice nuclei over an idealized mountain is simulated. The results show that, when the initial aerosol condition is changed from the relatively clean case to the polluted scenario, more droplets are activated, leading to a delay in precipitation, but the precipitation amount over the terrain is increased by about 10%. A detailed analysis of the microphysical processes indicates that ice-phase particles play an important role in cloud development, and their contribution to precipitation becomes more important with increasing aerosol particle concentrations. The growth of ice-phase particles through riming and Wegener-Bergeron-Findeisen regime is more effective under more polluted conditions, mainly due to the increased number of droplets with a diameter of 10-30 µm. Sensitivity tests also show that a tenfold increase in the concentration of ice crystals formed from ice nucleation leads to about 7% increase in precipitation, and the sensitivity of the precipitation to changes in the concentration and size distribution of aerosol particles is becoming less pronounced when the concentration of ice crystals is also increased.

  4. Semi-Empirical Validation of the Cross-Band Relative Absorption Technique for the Measurement of Molecular Mixing Ratios

    NASA Technical Reports Server (NTRS)

    Pliutau, Denis; Prasad, Narasimha S

    2013-01-01

    Studies were performed to carry out semi-empirical validation of a new measurement approach we propose for molecular mixing ratios determination. The approach is based on relative measurements in bands of O2 and other molecules and as such may be best described as cross band relative absorption (CoBRA). . The current validation studies rely upon well verified and established theoretical and experimental databases, satellite data assimilations and modeling codes such as HITRAN, line-by-line radiative transfer model (LBLRTM), and the modern-era retrospective analysis for research and applications (MERRA). The approach holds promise for atmospheric mixing ratio measurements of CO2 and a variety of other molecules currently under investigation for several future satellite lidar missions. One of the advantages of the method is a significant reduction of the temperature sensitivity uncertainties which is illustrated with application to the ASCENDS mission for the measurement of CO2 mixing ratios (XCO2). Additional advantages of the method include the possibility to closely match cross-band weighting function combinations which is harder to achieve using conventional differential absorption techniques and the potential for additional corrections for water vapor and other interferences without using the data from numerical weather prediction (NWP) models.

  5. Assessing filtering of mountaintop CO2 mixing ratios for application to inverse models of biosphere-atmosphere carbon exchange

    NASA Astrophysics Data System (ADS)

    Brooks, B.-G. J.; Desai, A. R.; Stephens, B. B.; Bowling, D. R.; Burns, S. P.; Watt, A. S.; Heck, S. L.; Sweeney, C.

    2011-09-01

    There is a widely recognized need to improve our understanding of biosphere-atmosphere carbon exchanges in areas of complex terrain including the United States Mountain West. CO2 fluxes over mountainous terrain are difficult to measure often due to unusual and complicated influences associated with atmospheric transport in complex terrain. Using five years of CO2 mixing ratio observations from the Regional Atmospheric Continuous CO2 Network in the Rocky Mountains (Rocky RACCOON), five statistical (subsetting) filters are used to investigate a range of approaches for identifying regionally representative CO2 mixing ratios. Test results from three filters indicate that subsets based on short-term variance and local CO2 gradients across tower inlet heights retain nine-tenths of the total observations and are able to define representative diurnal variability and seasonal cycles even for difficult-to-model sites where the influence of local fluxes is much larger than regional mixing ratio variations. Test results from two other filters that consider measurements from previous and following days using spline fitting or sliding windows are overly selective. Case study examples showed that even when standardized to common subset sizes these windowing-filters rejected measurements representing synoptic changes in CO2, which suggests that they are not well suited to filtering continental CO2 measurements. We present a novel CO2 lapse rate filter that uses CO2 differences between levels in the model atmosphere to constrain subsets of site measurements that are representative on model scales.

  6. Vertical and meridional distributions of the atmospheric CO2 mixing ratio between northern midlatitudes and southern subtropics

    NASA Astrophysics Data System (ADS)

    Machida, T.; Kita, K.; Kondo, Y.; Blake, D.; Kawakami, S.; Inoue, G.; Ogawa, T.

    2002-02-01

    The atmospheric CO2 mixing ratio was measured using a continuous measurement system onboard a Gulfstream-II aircraft between the northern midlatitudes and the southern subtropics during the Biomass Burning and Lightning Experiment Phase A (BIBLE A) campaign in September-October 1998. The vertical distribution of CO2 over tropical regions was almost constant from the surface to an altitude of 13 km. CO2 enhancements from biomass burning and oceanic release were observed in the tropical boundary layer. Measurements in the upper troposphere indicate interhemispheric exchange was effectively suppressed between 2°N-7°N. Interhemispheric transport of air in the upper troposphere was suppressed effectively in this region. The CO2 mixing ratios in the Northern and Southern Hemispheres were almost constant, with an average value of about 365 parts per million (ppm) and 366 ppm, respectively. The correlation between the CO2 and NOy mixing ratios observed north of 7°N was apparently different from that obtained south of 2°N. This fact strongly supports the result that the north-south boundary in the upper troposphere during BIBLE A was located around 2°N-7°N as the boundary is not necessary a permanent feature.

  7. Vertical and meridional distributions of the atmospheric CO2 mixing ratio between northern midlatitudes and southern subtropics

    NASA Astrophysics Data System (ADS)

    Machida, T.; Kita, K.; Kondo, Y.; Blake, D.; Kawakami, S.; Inoue, G.; Ogawa, T.

    2003-02-01

    The atmospheric CO2 mixing ratio was measured using a continuous measurement system onboard a Gulfstream-II aircraft between the northern midlatitudes and the southern subtropics during the Biomass Burning and Lightning Experiment Phase A (BIBLE A) campaign in September-October 1998. The vertical distribution of CO2 over tropical regions was almost constant from the surface to an altitude of 13 km. CO2 enhancements from biomass burning and oceanic release were observed in the tropical boundary layer. Measurements in the upper troposphere indicate interhemispheric exchange was effectively suppressed between 2°N-7°N. Interhemispheric transport of air in the upper troposphere was suppressed effectively in this region. The CO2 mixing ratios in the Northern and Southern Hemispheres were almost constant, with an average value of about 365 parts per million (ppm) and 366 ppm, respectively. The correlation between the CO2 and NOy mixing ratios observed north of 7°N was apparently different from that obtained south of 2°N. This fact strongly supports the result that the north-south boundary in the upper troposphere during BIBLE A was located around 2°N-7°N as the boundary is not necessary a permanent feature.

  8. Investigations of boundary layer structure, cloud characteristics and vertical mixing of aerosols at Barbados with large eddy simulations

    NASA Astrophysics Data System (ADS)

    Jähn, M.; Muñoz-Esparza, D.; Chouza, F.; Reitebuch, O.

    2015-08-01

    Large eddy simulations (LES) are performed for the area of the Caribbean island Barbados to investigate island effects on boundary layer modification, cloud generation and vertical mixing of aerosols. Due to the presence of a topographically structured island surface in the domain center, the model setup has to be designed with open lateral boundaries. In order to generate inflow turbulence consistent with the upstream marine boundary layer forcing, we use the cell perturbation method based on finite amplitude perturbations. In this work, this method is for the first time tested and validated for moist boundary layer simulations with open lateral boundary conditions. Observational data obtained from the SALTRACE field campaign is used for both model initialization and a comparison with Doppler wind lidar data. Several numerical sensitivity tests are carried out to demonstrate the problems related to "gray zone modeling" when using coarser spatial grid spacings beyond the inertial subrange of three-dimensional turbulence or when the turbulent marine boundary layer flow is replaced by laminar winds. Especially cloud properties in the downwind area west of Barbados are markedly affected in these kinds of simulations. Results of an additional simulation with a strong trade-wind inversion reveal its effect on cloud layer depth and location. Saharan dust layers that reach Barbados via long-range transport over the North Atlantic are included as passive tracers in the model. Effects of layer thinning, subsidence and turbulent downward transport near the layer bottom at z ~ 1800 m become apparent. The exact position of these layers and strength of downward mixing is found to be mainly controlled atmospheric stability (especially inversion strength) and wind shear. Comparisons of LES model output with wind lidar data show similarities in the formation of the daytime convective plume and the mean vertical wind structure.

  9. Measurements of CH4 Mixing Ratio and D/H and 13C/12C Isotope Ratios in Atmospheric Samples from Continental United States

    NASA Astrophysics Data System (ADS)

    Tyler, S. C.; Ajie, H. O.; Gotoh, A. A.; Rice, A. L.

    2002-12-01

    We report δD and δ13C measurements of atmospheric CH4 from air samples collected bi-weekly from fixed surface sites in the United States. Our fixed surface sites are located at the mid-continental site Niwot Ridge, CO (41°N, 105°W) and a Pacific coastal northern hemispheric site receiving strong westerlies, Montaña de Oro, CA (35°N, 121°W). Data from multiyear bi-weekly sampling provide information relating seasonal cycling of CH4 sources and sinks in background air, provide a record of long term trends in CH4 mixing and isotope ratio related to atmospheric CH4 loading, and may reveal information on regional sources of CH4. Measurements of δD-CH4 average -93+/-3‰ (versus V-SMOW) at Niwot Ridge from 1999 through 2001 and -97+/-4‰ at Montaña de Oro from 2000 through 2001. Annual seasonal cycles observed at both sites are 6-7‰ , exhibiting strong anti-correlation with CH4 mixing ratio seasonality that appears to be largely sink-driven (i.e. through reaction with OH). More extensive time series in δ13C-CH4 average -47.2+/-0.1‰ (versus V-PDB) at Niwot Ridge from 1995 through 2001 and -47.3+/-0.2‰ at Montaña de Oro from 1996 through 2001. In contrast to δD-CH4, seasonality in δ13C-CH4 has a relatively poor anti-correlation with seasonality in CH4 mixing ratio, indicating significant source-driven influence. We discuss the implications of these measurements on the atmospheric CH4 budget and detail the precision and accuracy of our data with respect international reference standards. It is our intention to have these data archived and available for modeling and advanced calculations by other atmospheric researchers in the near future.

  10. The Houston Urban Heat Island: Surface Temperature, Aerosol Mixing Layer Height, and Surface Wind Field Relationships

    NASA Astrophysics Data System (ADS)

    Darby, L. S.; Senff, C. J.

    2007-12-01

    Both Dallas and Houston, Texas have comprehensive networks of surface meteorology and chemistry sensors. The similarities of the networks and lack of terrain in Dallas and Houston allow for the comparison of their urban heat islands (UHI). The Dallas UHI, unperturbed by thermal flows driven by the land/sea temperature difference, is a well-defined phenomenon over the summers of 2000-2006. Including all weather conditions, the average nighttime T(urban) - T(rural) temperature difference was between 1.5° and 2.0° C and the average daytime difference was ~ 1.0° C. Analysis of Houston temperature data, however, revealed a different picture due to the bay and gulf breezes. While the Houston UHI was a distinct phenomenon, even when including all weather conditions, the bay or gulf breeze modified the Houston UHI by cooling the city. Average nighttime T(urban) - T(rural) temperature differences in Houston were between 1.75° and 2.75° C. However, during the day, the rural areas to the north and west of the city were often warmer than the downtown area during afternoon hours as a result of the sea breeze. Averaging the Houston T(urban) - T(rural) temperature differences over the summers of 2000-2006 indicated a very small urban-rural temperature difference between 1400 to 1600 LST. In some individual years, such as 2000, 2003, 2005 and 2006, the urban areas were actually cooler than the rural areas, on average, in the mid-afternoon. These years had more bay breeze/gulf breeze activity to cool the urban area. We will also look at how land use, the UHI, and boundary-layer winds impact the horizontal distribution of boundary layer heights over the Houston area, as calculated from backscatter measurements from TOPAZ, an ozone and aerosol profiling lidar deployed on a NOAA Twin Otter in the summer of 2006 during the Texas Air Quality Study II.

  11. Nuclear Data Matters - The obvious case of a bad mixing ratio for 58Co

    SciTech Connect

    Hoffman, R. D.; Nesaraja, Caroline D.; Mattoon, Caleb

    2015-05-13

    We present results of modeled cross sections for neutron- and proton-induced reactions leading to the final product nucleus 58Co. In each case the gamma-cascade branching ratios given in the ENSDF database circa 2014 predict modeled nuclear cross sections leading to the ground and first excited metastable state that are incompatible with measured cross sections found in the NNDC experimental cross section database EXFOR. We show that exploring the uncertainty in the mixing ratio used to calculate the gamma-cascade branching ratios for the 53.15 keV 2nd excited state leads to changes in the predicted partial cross sections by amounts that give good agreement with measured data.

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

    NASA Astrophysics Data System (ADS)

    Burton, S. P.; Ferrare, R. A.; Omar, A. H.; Hostetler, C. A.; Hair, J. W.; Rogers, R.; Obland, M. D.; Butler, C. F.; Cook, A. L.; Harper, D. B.

    2012-12-01

    The NASA Langley Research Center (LaRC) airborne High Spectral Resolution Lidar (HSRL-1) on the NASA B200 aircraft has acquired large datasets of aerosol extinction (532nm), backscatter (532 and 1064nm), and depolarization (532 and 1064nm) profiles during 349 science flights in 19 field missions across North America since 2006. The extinction-to-backscatter ratio ("lidar ratio"), aerosol depolarization ratios, and backscatter color ratio measurements from HSRL-1 are scale-invariant parameters that depend on aerosol type but not concentration. These four aerosol intensive parameters are combined to qualitatively classify HSRL aerosol measurements into eight separate composition types. The classification methodology uses models formed from "training cases" with known aerosol type. The remaining measurements are then compared with these models using the Mahalanobis distance. Aerosol products from the CALIPSO satellite include aerosol type information as well, which is used as input to the CALIPSO aerosol retrieval. CALIPSO aerosol types are inferred using a mix of aerosol loading-dependent parameters, estimated aerosol depolarization, and location, altitude, and surface type information. The HSRL instrument flies beneath the CALIPSO satellite orbit track, presenting the opportunity for comparisons between the HSRL aerosol typing and the CALIPSO Vertical Feature Mask Aerosol Subtype product, giving insight into the performance of the CALIPSO aerosol type algorithm. We find that the aerosol classification from the two instruments frequently agree for marine aerosols and pure dust, and somewhat less frequently for pollution and smoke. In addition, the comparison suggests that the CALIPSO polluted dust type is overly inclusive, encompassing cases of dust combined with marine aerosol as well as cases without much evidence of dust. Qualitative classification of aerosol type combined with quantitative profile measurements of aerosol backscatter and extinction has many useful

  13. Black carbon aerosol in winter northeastern Qinghai-Tibetan Plateau, China: the source, mixing state and optical property

    NASA Astrophysics Data System (ADS)

    Wang, Q. Y.; Huang, R.-J.; Cao, J. J.; Tie, X. X.; Ni, H. Y.; Zhou, Y. Q.; Han, Y. M.; Hu, T. F.; Zhu, C. S.; Feng, T.; Li, N.; Li, J. D.

    2015-11-01

    Black carbon (BC) aerosol at high altitudes of the Qinghai-Tibetan Plateau has potential effects on the regional climate and hydrological cycle. An intensive measurement campaign was conducted at Qinghai Lake (~ 3200 m above sea level) at the edge of the northeastern Qinghai-Tibetan Plateau during winter using a ground-based single particle soot photometer (SP2) and a photoacoustic extinctiometer (PAX). The average concentration of refractory BC (rBC) and number fraction of coated rBC were found to be 160 ± 190 ng m-3 and 59 % for the entire campaign, respectively. Significant enhancements of rBC loadings and number fraction of coated rBC were observed during a pollution episode, with an average value of 390 ng m-3 and 65 %, respectively. The mass size distribution of rBC particles showed log-normal distribution, with a peak diameter of ~ 187 nm regardless of the pollution level. Five-day backward trajectory analysis suggests that the air masses from north India contributed to the increased rBC loadings during the campaign. The potential source contribution function (PSCF) model combined with the fire counts map further proves that biomass burning from north India is an important potential source influencing the northeastern Qinghai-Tibetan Plateau during the pollution episode. The rBC mass absorption cross section (MACrBC) at λ = 532 nm was slightly larger in clean days (14.9 m2 g-1) than during the pollution episode (9.3 m2 g-1), likely due to the effects of brown carbon and the uncertainty of the MACrBC calculation. The MACrBC was positively correlated with number fraction of coated rBC during the pollution episode with an increasing rate of 0.18 (m2 g-1) %-1. The number fraction of coated rBC particles showed positive correlation with light absorption, suggesting that the increase of coated rBC particles will enhance the light absorption. Compared to rBC mass concentration, rBC mixing sate is more important in determining absorption during the pollution

  14. A Tropical Lake Breeze System : The Effect on Surface NO, NO2, O3, and CO2 Mixing Ratios

    NASA Astrophysics Data System (ADS)

    Lima Moura, M. A.; Eça D'Almeida Rocha, C. H.; Trebs, I.; Andreae, M. O.; Meixner, F. X.

    2003-04-01

    During the Cooperative LBA Airborne Regional Experiment 2001 (CLAIRE2001, July 2001), we investigated diel variations of nitric oxide (NO), nitrogen dioxide (NO_2), ozone (O_3) and carbon dioxide (CO_2) mixing ratios at Balbina Limnological Station (01^o55'994''S, 59^o28'071''W, Amazonia,Brazil). We applied sensitive and species-specific chemiluminescence (NO, NO_2, O_3) and NDIR (CO_2) analysers to record ambient mixing ratios on 1 min intervals. Simultaneously, we extensively monitored (micro-)meteorological qauntities (air temperature, relative humidity, wind speed and -direction, thermal stratification, rainfall intensity, soil temperatures and moisture, as well as radiation fluxes (global, net, short wave, NO_2 photolysis, and photosynthetic active)). Balbina Limnological Station is located just a few hundred meters south of a 2.360 km^2 hydroelectric power dam (Usina Hidrelétrica de Balbina) and about 100m north from the edge of a primary rainforest. Marked differences in surface albedo and heat storage capacity generate a local wind system, the lake breeze, which advects air from the dam (09:00 to 15:00 local) and from the rainforest (18:00 to 06:00 local), respectively. Generally, we observed marked diel variations of NO, NO_2, O_3, and CO_2 (high/low levels during night/day) and O_3 (low/high levels during night/day). Especially in the tropics, this behaviour is usually related to (a) accumulation of soil emissions (NO, CO_2), chemical reactions (NO, from NO_2-O_3 reaction) and surface destruction (O_3) in a shallow and strong nocturnal boundary layer inversion, and (b) to soil emission (NO), photochemical reactions (NO-NO_2-O_3), dry deposition/plant uptake (NO_2, O_3, and CO_2) and strong turbulent vertical mixing in the daytime mixed layer. However, under the specific conditions of the lake breeze soil emission and dry deposition/ plant uptake can be neglected during daytime. Consequently, the investigation of daytime mixing ratios can be confined to

  15. Deliquescence behavior of internally mixed clay and salt aerosols by optical extinction measurements.

    PubMed

    Attwood, Alexis Rae; Greenslade, Margaret E

    2012-05-10

    Internal mixtures of montmorillonite, a clay component of mineral dust, with sodium chloride or ammonium sulfate were studied optically using cavity ring down spectroscopy. The effects of the addition of the clay to the optically observed deliquescence relative humidity (DRH) and water uptake of these salts were considered by investigating a series of different salt mass fractions. In most cases, montmorillonite alters the hygroscopic properties, lowering the DRH in comparison to the pure salt, and causes the particles to transition from solid to liquid at a lower relative humidity than is expected based on the salt alone. Predictions based on volume-weighted mixing rules were not accurate for most measurements around the DRH. We attribute deviations from theory to changes in the Gibbs free energy of the system caused by disturbances in the ion-ion interactions and lattice structure allowing water uptake prior to the DRH of the salt. Our optical results contradict some current measurements in the literature that suggest little change in the hygroscopic behavior of salts when insoluble mineral dust components are added.

  16. Investigating Primary Marine Aerosol Properties: CCN Activity of Sea Salt and Mixed Inorganic–Organic Particles

    PubMed Central

    2012-01-01

    Sea spray particles ejected as a result of bubbles bursting from artificial seawater containing salt and organic matter in a stainless steel tank were sampled for size distribution, morphology, and cloud condensation nucleus (CCN) activity. Bubbles were generated either by aeration through a diffuser or by water jet impingement on the seawater surface. Three objectives were addressed in this study. First, CCN activities of NaCl and two types of artificial sea salt containing only inorganic components were measured to establish a baseline for further measurements of mixed organic–inorganic particles. Second, the effect of varying bubble residence time in the bulk seawater solution on particle size and CCN activity was investigated and was found to be insignificant for the organic compounds studied. Finally, CCN activities of particles produced from jet impingement were compared with those produced from diffuser aeration. Analyses indicate a considerable amount of organic enrichment in the jet-produced particles relative to the bulk seawater composition when sodium laurate, an organic surfactant, is present in the seawater. In this case, the production of a thick foam layer during impingement may explain the difference in activation and supports hypotheses that particle production from the two methods of generating bubbles is not equal. PMID:22809370

  17. Evolution of biomass burning aerosol over the Amazon: airborne measurements of aerosol chemical composition, microphysical properties, mixing state and optical properties during SAMBBA

    NASA Astrophysics Data System (ADS)

    Morgan, W.; Allan, J. D.; Flynn, M.; Darbyshire, E.; Hodgson, A.; Liu, D.; O'Shea, S.; Bauguitte, S.; Szpek, K.; Johnson, B.; Haywood, J.; Longo, K.; Artaxo, P.; Coe, H.

    2013-12-01

    Biomass burning represents one of the largest sources of particulate matter to the atmosphere, resulting in a significant perturbation to the Earth's radiative balance coupled with serious impacts on public health. On regional scales, the impacts are substantial, particularly in areas such as the Amazon Basin where large, intense and frequent burning occurs on an annual basis for several months. Absorption by atmospheric aerosols is underestimated by models over South America, which points to significant uncertainties relating to Black Carbon (BC) aerosol properties. Initial results from the South American Biomass Burning Analysis (SAMBBA) field experiment, which took place during September and October 2012 over Brazil on-board the UK Facility for Airborne Atmospheric Measurement (FAAM) BAe-146 research aircraft, are presented here. Aerosol chemical composition was measured by an Aerodyne Aerosol Mass Spectrometer (AMS) and a DMT Single Particle Soot Photometer (SP2). The physical, chemical and optical properties of the aerosols across the region will be characterized in order to establish the impact of biomass burning on regional air quality, weather and climate. The aircraft sampled a range of conditions including sampling of pristine Rainforest, fresh biomass burning plumes, regional haze and elevated biomass burning layers within the free troposphere. The aircraft sampled biomass burning aerosol across the southern Amazon in the states of Rondonia and Mato Grosso, as well as in a Cerrado (Savannah-like) region in Tocantins state. This presented a range of fire conditions, in terms of their number, intensity, vegetation-type and their combustion efficiencies. Near-source sampling of fires in Rainforest environments suggested that smouldering combustion dominated, while flaming combustion dominated in the Cerrado. This led to significant differences in aerosol chemical composition, particularly in terms of the BC content, with BC being enhanced in the Cerrado

  18. Modelling lactation curve for milk fat to protein ratio in Iranian buffaloes (Bubalus bubalis) using non-linear mixed models.

    PubMed

    Hossein-Zadeh, Navid Ghavi

    2016-08-01

    The aim of this study was to compare seven non-linear mathematical models (Brody, Wood, Dhanoa, Sikka, Nelder, Rook and Dijkstra) to examine their efficiency in describing the lactation curves for milk fat to protein ratio (FPR) in Iranian buffaloes. Data were 43 818 test-day records for FPR from the first three lactations of Iranian buffaloes which were collected on 523 dairy herds in the period from 1996 to 2012 by the Animal Breeding Center of Iran. Each model was fitted to monthly FPR records of buffaloes using the non-linear mixed model procedure (PROC NLMIXED) in SAS and the parameters were estimated. The models were tested for goodness of fit using Akaike's information criterion (AIC), Bayesian information criterion (BIC) and log maximum likelihood (-2 Log L). The Nelder and Sikka mixed models provided the best fit of lactation curve for FPR in the first and second lactations of Iranian buffaloes, respectively. However, Wood, Dhanoa and Sikka mixed models provided the best fit of lactation curve for FPR in the third parity buffaloes. Evaluation of first, second and third lactation features showed that all models, except for Dijkstra model in the third lactation, under-predicted test time at which daily FPR was minimum. On the other hand, minimum FPR was over-predicted by all equations. Evaluation of the different models used in this study indicated that non-linear mixed models were sufficient for fitting test-day FPR records of Iranian buffaloes.

  19. SAM II aerosol profile measurements, Poker Flat, Alaska; July 16-19, 1979

    NASA Technical Reports Server (NTRS)

    Mccormick, M. P.; Chu, W. P.; Mcmaster, L. R.; Grams, G. W.; Herman, B. M.; Pepin, T. J.; Russell, P. B.; Swissler, T. J.

    1981-01-01

    SAM II satellite measurements during the July 1979 Poker Flat mission, yielded an aerosol extinction coefficient of 0.0004/km at 1.0 micron wavelength, in the region of the stratospheric aerosol mixing ratio peak (12-16 km). The stratospheric aerosol optical depth for these data, calculated from the tropopause through 30 km, is approximately 0.001. These results are consistent with the average 1979 summertime values found throughout the Arctic.

  20. 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.

  1. LASE measurements of aerosols and water vapor during TARFOX

    NASA Technical Reports Server (NTRS)

    Ferrare, Richard A.; Ismail, Syed; Browell, Edward V.; Brackett, Vincent G.; Kooi, Susan A.; Clayton, Marian B.; Melfi, Harvey; Whiteman, David N.; Schwenner, Geary; Evans, Keith D.; Hobbs, Peter V.; Veefkind, J. Pepijn; Russell, Philip B.; Livingston, John M.; Hignett, Philip; Holben, Brent N.; Remer, Lorraine A.

    1998-01-01

    The TARFOX (Tropospheric Aerosol Radiative Forcing Observational Experiment) intensive field campaign was designed to reduce uncertainties in estimates of the effects of anthropogenic aerosols on climate by measuring direct radiative effects and the optical, physical, and chemical properties of aerosols [1]. TARFOX was conducted off the East Coast of the United States between July 10-31, 1996. Ground, aircraft, and satellite-based sensors measured the sensitivity of radiative fields at various atmospheric levels to aerosol optical properties (i.e., optical thickness, phase function, single-scattering albedo) and to the vertical profile of aerosols. The LASE (Lidar Atmospheric Sensing Experiment) instrument, which was flown on the NASA ER-2 aircraft, measured vertical profiles of total scattering ratio and water vapor during a series of 9 flights. These profiles were used in real-time to help direct the other aircraft to the appropriate altitudes for intensive sampling of aerosol layers. We have subsequently used the LASE aerosol data to derive aerosol backscattering and extinction profiles. Using these aerosol extinction profiles, we derived estimates of aerosol optical thickness (AOT) and compared these with measurements of AOT from both ground and airborne sun photometers and derived from the ATSR-2 (Along Track and Scanning Radiometer 2) sensor on ERS-2 (European Remote Sensing Satellite-2). We also used the water vapor mixing ratio profiles measured simultaneously by LASE to derive precipitable water vapor and compare these to ground based measurements.

  2. FORMATION CONDITIONS OF ICY MATERIALS IN COMET C/2004 Q2 (MACHHOLZ). I. MIXING RATIOS OF ORGANIC VOLATILES

    SciTech Connect

    Kobayashi, Hitomi; Kawakita, Hideyo

    2009-09-20

    We observed comet C/2004 Q2 (Machholz) with the Keck II telescope in late 2005 January and we obtained the spectra of C/2004 Q2 including many emission lines of volatile species such as H{sub 2}O, HCN, C{sub 2}H{sub 2}, NH{sub 3}, CH{sub 4}, C{sub 2}H{sub 6}, CH{sub 3}OH, and H{sub 2}CO with high-signal-to-noise ratios. Based on our observations, we determined the mixing ratios of the molecules relative to H{sub 2}O in C/2004 Q2. Since C/2004 Q2 is one of Oort Cloud comets, it is interesting to compare our results with other Oort Cloud comets. The mixing ratios of C{sub 2}H{sub 2}/H{sub 2}O and C{sub 2}H{sub 6}/H{sub 2}O in C/2004 Q2 are lower than typical Oort Cloud comets. Especially, C{sub 2}H{sub 2}/H{sub 2}O ratio in C/2004 Q2 is as lower as Jupiter Family comets. However, mixing ratios of other molecules in C/2004 Q2 are similar to typical Oort Cloud comets. C/2004 Q2 might be the intermediate type between Oort Cloud and Jupiter Family comets. To investigate the formation conditions of such intermediate type comet, we focused on the (C{sub 2}H{sub 2}+C{sub 2}H{sub 6})/H{sub 2}O ratios and C{sub 2}H{sub 6}/(C{sub 2}H{sub 6}+C{sub 2}H{sub 2}) ratios in comets from the viewpoint of conversion from C{sub 2}H{sub 2} to C{sub 2}H{sub 6} in the precometary ices. We found that (C{sub 2}H{sub 2}+C{sub 2}H{sub 6})/H{sub 2}O ratio in C/2004 Q2 is lower than the ratio in typical Oort Cloud comets while C{sub 2}H{sub 6}/(C{sub 2}H{sub 6}+C{sub 2}H{sub 2}) ratio in C/2004 Q2 is consistent with the ratio of the typical Oort Cloud comets and Jupiter family comets. If we assume that the cometary volatiles such as H{sub 2}O, CH{sub 4}, and C{sub 2}H{sub 2} formed similar environment, the C{sub 2}H{sub 6}/(C{sub 2}H{sub 6}+C{sub 2}H{sub 2}) ratio might not be sensitive in the temperature range where hydrogen-addition reactions occurred and cometesimals formed ({approx}30 K). We employed the dynamical-evolutional model and the chemical-evolutional model to determine the

  3. Single-particle characterization of biomass burning organic aerosol (BBOA): evidence for non-uniform mixing of high molecular weight organics and potassium

    NASA Astrophysics Data System (ADS)

    Lee, Alex K. Y.; Willis, Megan D.; Healy, Robert M.; Wang, Jon M.; Jeong, Cheol-Heon; Wenger, John C.; Evans, Greg J.; Abbatt, Jonathan P. D.

    2016-05-01

    Biomass burning organic aerosol (BBOA) can be emitted from natural forest fires and human activities such as agricultural burning and domestic energy generation. BBOA is strongly associated with atmospheric brown carbon (BrC) that absorbs near-ultraviolet and visible light, resulting in significant impacts on regional visibility degradation and radiative forcing. The mixing state of BBOA can play a critical role in the prediction of aerosol optical properties. In this work, single-particle measurements from a Soot-Particle Aerosol Mass Spectrometer coupled with a light scattering module (LS-SP-AMS) were performed to examine the mixing state of BBOA, refractory black carbon (rBC), and potassium (K, a tracer for biomass burning aerosol) in an air mass influenced by wildfire emissions transported from northern Québec to Toronto, representing aged biomass burning plumes. Cluster analysis of single-particle measurements identified five BBOA-related particle types. rBC accounted for 3-14 wt % of these particle types on average. Only one particle type exhibited a strong ion signal for K+, with mass spectra characterized by low molecular weight organic species. The remaining four particle types were classified based on the apparent molecular weight of the BBOA constituents. Two particle types were associated with low potassium content and significant amounts of high molecular weight (HMW) organic compounds. Our observations indicate non-uniform mixing of particles within a biomass burning plume in terms of molecular weight and illustrate that HMW BBOA can be a key contributor to low-volatility BrC observed in BBOA particles. The average mass absorption efficiency of low-volatility BBOA is about 0.8-1.1 m2 g-1 based on a theoretical closure calculation. Our estimates indicate that low-volatility BBOA contributes ˜ 33-44 % of thermo-processed particle absorption at 405 nm; and almost all of the BBOA absorption was associated with low-volatility organics.

  4. X-ray attenuation measurements in a cavitating mixing layer for instantaneous two-dimensional void ratio determination

    SciTech Connect

    Aeschlimann, Vincent; Barre, Stephane; Legoupil, Samuel

    2011-05-15

    The purpose of this experimental study was to analyze a two-dimensional cavitating shear layer. The global aim of this work was to obtain a better understanding and modeling of cavitation phenomenon in a 2D turbulent sheared flow which can be considered as quite representative of cavitating rocket engine turbopomp inducers. This 2D mixing layer flow provided us a well documented test case which can be used for the characterization of the cavitation effects in sheared flows. The development of a velocity gradient was observed inside a liquid water flow: Kelvin-Helmholtz instabilities developed at the interface. Vaporizations and implosions of cavitating structures inside the vortices were observed. X-ray attenuation measurements were performed to estimate the amount of vapor present inside the mixing area. Instantaneous two-dimensional void ratio fields were acquired. The real spatial resolutions are 0.5 mm with 2000 fps and 1.5 mm with 20 000 fps. The effective time resolution is equal to the camera frame rate up to a 19% void ratio variation between two consecutive images. This seems to be sufficient in the context of the present flow configuration. The two-phase structures present inside the mixing area were analyzed at three different cavitation levels and their behaviors were compared to non-cavitating flow dynamic. Convection velocities and vortices shedding frequencies were estimated. Results show that vapor was transported by the turbulent velocity field. Statistical analysis of the void ratio signal was carried out up to the fourth order moment. This study provided a global understanding of the cavitating structure evolution and of the cavitation effects on turbulent sheared flows.

  5. Hygroscopicity of organic compounds from biomass burning and their influence on the water uptake of mixed organic-ammonium sulfate aerosols

    NASA Astrophysics Data System (ADS)

    Lei, T.; Zuend, A.; Wang, W. G.; Zhang, Y. H.; Ge, M. F.

    2014-05-01

    Hygroscopic behavior of organic compounds, including levoglucosan, 4-hydroxybenzoic acid and humic acid, and their effects on the hygroscopic properties of ammonium sulfate (AS) in internally mixed particles are studied by a hygroscopicity tandem differential mobility analyzer (HTDMA). The organic compounds used represent pyrolysis products of wood that are emitted from biomass burning sources. It is found that humic acid aerosol particles only slightly take up water, starting at RH above ∼70%. This is contrasted by the continuous water absorption of levoglucosan aerosol particles in the range 5-90% RH. However, no hygroscopic growth is observed for 4-hydroxybenzoic acid aerosol particles. Predicted water uptake using the ideal solution theory, the AIOMFAC model and the E-AIM (with UNIFAC) model are consistent with measured hygroscopic growth factors of levoglucosan. However, the use of these models without consideration of crystalline organic phases is not appropriate to describe the hygroscopicity of organics that do not exhibit continuous water uptake, such as 4-hydroxybenzoic acid and humic acid. Mixed aerosol particles consisting of ammonium sulfate and levoglucosan, 4-hydroxybenzoic acid, or humic acid with different organic mass fractions, take up a reduced amount of water above 80% RH (above AS deliquescence) relative to pure ammonium sulfate aerosol particles of the same mass. Hygroscopic growth of mixtures of ammonium sulfate and levoglucosan with different organic mass fractions agree well with the predictions of the thermodynamic models. Use of the Zdanovskii-Stokes-Robinson (ZSR) relation and AIOMFAC model lead to good agreement with measured growth factors of mixtures of ammonium sulfate with 4-hydrobenxybenzoic acid assuming an insoluble organic phase. Deviations of model predictions from the HTDMA measurement are mainly due to the occurrence of a microscopical solid phase restructuring at increased humidity (morphology effects), which are not

  6. Investigating primary marine aerosol properties: CCN activity of sea salt and mixed particles

    NASA Astrophysics Data System (ADS)

    King, S. M.; Butcher, A. C.; Rosenoern, T.; Coz, E.; Lieke, K. I.; de Leeuw, G.; Nilsson, E. D.; Bilde, M.

    2012-04-01

    Sea salt particles ejected as a result of bubbles bursting from artificial seawater in a closed stainless steel tank were sampled for size distribution, morphology, and cloud condensation nucleus (CCN) activity. The two-component artificial seawater consisted of salt, either NaCl or sea salt, and one organic compound in deionized water. Several organic molecules representative of oceanic organic matter were investigated. Bubbles were generated either by aeration through a porous diffuser or by water jet impingement on the surface of the artificial seawater. The effect of bubble lifetime, which was controlled by varying the depth of the diffuser in the water column, on particle size and CCN activity was investigated and was found to be insignificant for the organic compounds studied. The CCN activities of particles produced from diffuser-generated bubbles were generally governed by the high hygroscopicity of salt, such that activation was indistinguishable from that of salt, except in the case of very low mass ratio of salt to organic matter in the seawater solution. There was, however, a considerable decrease in CCN activity for particles produced from jet impingement on seawater that had a salinity of 10‰ and contained 0.45 mM of sodium laurate, an organic surfactant. The production of a thick foam layer from impingement may explain the difference in activation and supports hypotheses that particle production from the two methods of generating bubbles is not similar. Accurate conclusions from observed CCN activities of particles from artificial seawater containing organic matter require knowledge of the CCN activity of the inorganic component, especially as a small amount of the inorganic can heavily influence activation. Therefore, the CCN activity of both artificial sea salt and NaCl were measured and compared. Part of the discrepancy observed between the CCN activities of the two salts may be due to morphological differences, which were investigated using

  7. Mean ocean temperature change over the last glacial transition based on atmospheric changes in heavy noble mixing ratios

    NASA Astrophysics Data System (ADS)

    Bereiter, Bernhard; Severinghaus, Jeff; Shackleton, Sarah; Baggenstos, Daniel; Kawamura, Kenji

    2016-04-01

    On paleo-climatic timescales heavy noble gases (Krypton and Xenon) are passively cycled through the atmosphere-ocean system without seeing any significant sink or source. Since the solubility in water of each gas species is characterized by a specific temperature dependency, mixing ratios in the atmosphere change with changing ocean temperatures. In this study, we use this fact to reconstruct mean global ocean temperatures (MOT) over the course of the last glacial transition based on measurements of trapped air in the WAIS Divide ice core. We analyzed 70 ice samples with a recently developed method which determines the isotopic ratios of N2, Ar, Kr (and in some cases also of Xe, though with less precision) and the elemental ratios of Kr/N2, Xe/N2 and Xe/Kr. We use the isotope ratios to correct the elemental ratios for gravitational enrichment in the firn column. The corrected elemental ratios are then used in a simple box model to reconstruct MOT. The three elemental ratio pairs are first interpreted as independent measures of MOT and then combined to a single "best-estimate" MOT record with an average uncertainty of 0.27°C. We find a clear link to Antarctic temperatures and a LGM-Holocene change in MOT of 2.4°C. This value is in good agreement with results from marine sediment cores (which, however, have an uncertainty of 1°C). Our record provides an unprecedented constrain on ocean heat uptake over the last glacial transition and therefore gives new insights in the mechanisms underlying long term ocean heat fluxes. To our knowledge, this is the first time that MOT has been reconstructed in such great detail.

  8. On atmospheric lidar performance comparison: from power aperture product to power aperture mixing ratio scattering cross-section product

    NASA Astrophysics Data System (ADS)

    She, Chiao-Yao

    2005-12-01

    A new performance index for atmospheric lidar, namely the power aperture mixing ratio scattering cross-section (PAMS) product, is proposed. Unlike the index widely used at present, namely the power aperture (PA) product, the new index provides an accurate comparison between different types of lidar for measuring the same atmospheric parameters. Using a sodium resonance lidar and a ‘Rayleigh’ lidar for measuring temperature and wind in the mesopause region (80 105 km) as an example, the concept and application of PAMS are illustrated.

  9. Abundance of fluorescent biological aerosol particles at temperatures conducive to the formation of mixed-phase and cirrus clouds

    NASA Astrophysics Data System (ADS)

    Twohy, Cynthia H.; McMeeking, Gavin R.; DeMott, Paul J.; McCluskey, Christina S.; Hill, Thomas C. J.; Burrows, Susannah M.; Kulkarni, Gourihar R.; Tanarhte, Meryem; Kafle, Durga N.; Toohey, Darin W.

    2016-07-01

    Some types of biological particles are known to nucleate ice at warmer temperatures than mineral dust, with the potential to influence cloud microphysical properties and climate. However, the prevalence of these particle types above the atmospheric boundary layer is not well known. Many types of biological particles fluoresce when exposed to ultraviolet light, and the Wideband Integrated Bioaerosol Sensor takes advantage of this characteristic to perform real-time measurements of fluorescent biological aerosol particles (FBAPs). This instrument was flown on the National Center for Atmospheric Research Gulfstream V aircraft to measure concentrations of fluorescent biological particles from different potential sources and at various altitudes over the US western plains in early autumn. Clear-air number concentrations of FBAPs between 0.8 and 12 µm diameter usually decreased with height and generally were about 10-100 L-1 in the continental boundary layer but always much lower at temperatures colder than 255 K in the free troposphere. At intermediate temperatures where biological ice-nucleating particles may influence mixed-phase cloud formation (255 K ≤ T ≤ 270 K), concentrations of fluorescent particles were the most variable and were occasionally near boundary-layer concentrations. Predicted vertical distributions of ice-nucleating particle concentrations based on FBAP measurements in this temperature regime sometimes reached typical concentrations of primary ice in clouds but were often much lower. If convection was assumed to lift boundary-layer FBAPs without losses to the free troposphere, better agreement between predicted ice-nucleating particle concentrations and typical ice crystal concentrations was achieved. Ice-nucleating particle concentrations were also measured during one flight and showed a decrease with height, and concentrations were consistent with a relationship to FBAPs established previously at the forested surface site below. The vertical

  10. Collection efficiency of the soot-particle aerosol mass spectrometer (SP-AMS) for internally mixed particulate black carbon

    DOE PAGES

    Willis, M. D.; Lee, A. K. Y.; Onasch, T. B.; ...

    2014-12-18

    The soot-particle aerosol mass spectrometer (SP-AMS) uses an intra-cavity infrared laser to vaporize refractory black carbon (rBC) containing particles, making the particle beam–laser beam overlap critical in determining the collection efficiency (CE) for rBC and associated non-refractory particulate matter (NR-PM). This work evaluates the ability of the SP-AMS to quantify rBC and NR-PM mass in internally mixed particles with different thicknesses of organic coating. Using apparent relative ionization efficiencies for uncoated and thickly coated rBC particles, we report measurements of SP-AMS sensitivity to NR-PM and rBC, for Regal Black, the recommended particulate calibration material. Beam width probe (BWP) measurements aremore » used to illustrate an increase in sensitivity for highly coated particles due to narrowing of the particle beam, which enhances the CE of the SP-AMS by increasing the laser beam–particle beam overlap. Assuming complete overlap for thick coatings, we estimate CE for bare Regal Black particles of 0.6 ± 0.1, which suggests that previously measured SP-AMS sensitivities to Regal Black were underestimated by up to a factor of 2. The efficacy of the BWP measurements is highlighted by studies at a busy road in downtown Toronto and at a non-roadside location, which show particle beam widths similar to, but greater than that of bare Regal Black and coated Regal Black, respectively. Further BWP measurements at field locations will help to constrain the range of CE for fresh and aged rBC-containing particles. The ability of the SP-AMS to quantitatively assess the composition of internally mixed particles is validated through measurements of laboratory-generated organic coated particles, which demonstrate that the SP-AMS can quantify rBC and NR-PM over a wide range of particle compositions and rBC core sizes.« less

  11. Optimization of the mixing ratio of ice crystal shapes in cirrus clouds for atmospheric point spread function modeling

    NASA Astrophysics Data System (ADS)

    Muguet, Isabelle; Chervet, Patrick; Rozé, Claude

    2007-10-01

    A critical issue to calculate the image transmission through cirrus clouds is to obtain a detailed description of the angular distribution of the scattered radiation in the forward direction. Computation of the scattering phase function on the basis of microphysics description of the cloud thanks to ray-tracing codes, seems to be the best way to fulfill this requirement. However, a comprehensive microphysical model can not be found, because of the great variability of the ice crystals composing natural cirrus. An optimization process has been developed to find the best mixing ratio of four pristine ice crystals shapes that minimizes the error on the forward peak of the scattering phase function. To achieve this goal, a comparison with a reference phase function derived from MODIS database has been led. The bulk scattering properties of the seven size distributions defined in this database have been computed at four wavelengths in the spectral domain from visible to medium infrared, applying the mixing ratio obtained after an optimization at 0.55μm. Used as an input to a propagation model based on a Monte Carlo method, PSF have been computed. They show very good agreement with the PSF calculated with the corresponding reference scattering properties.

  12. Recyclability of bottom ash mixed with dredged soils according to the transportation distance and mixing ratio through the estimation of CO2 emissions.

    PubMed

    Noh, Sookack; Son, Younghwan; Yoon, Taegang; Bong, Taeho

    2015-06-01

    Bottom ash and dredged soils can be used as construction materials because they are similar in physical characteristics to natural aggregates. However, whenever such byproducts as bottom ash and dredged soils are used, the energy efficiency of recycling is offset to a certain degree by emissions from transportation. The objective of this study is to analyze the environmental efficiency of recycling bottom ash and dredged soils through the estimation of CO2 emissions, considering both transportation distance and the mixing ratio. Agricultural reservoirs were selected as the final destinations of these recycled materials. This analysis demonstrated that using 100% bottom ash emits less CO2 than using natural aggregates when the ash is transported less than 35.15 km. This breakeven distance increases exponentially with the mass fraction of admixed dredged soil. However, admixture with natural soils does not affect the breakeven distance. Using the breakeven distances, the effective area with which it is efficient to recycle bottom ash was delineated. When dredged soil is admixed to a mass fraction of 70%, the effective area covers most of South Korea. In addition, 100% bottom ash was efficient in 1622 reservoirs (9.45%) in terms of CO2 emissions, and the mixture with 30% bottom ash and 70% dredged soils is efficient in 98.83% of all of the reservoirs in Korea. Bottom ash is most useful for reducing CO2 emissions when it is mixed with dredged soils, which are a byproduct of construction found on-site. This result is meaningful because bottom ash and dredged soils are complementary in their physical characteristics, and they need to be mixed before use as construction materials. The recycling of bottom ash becomes even more attractive with anticipated improvements in fuel efficiency.

  13. Mixing characteristics of a moderate aspect ratio screeching supersonic rectangular jet

    NASA Astrophysics Data System (ADS)

    Valentich, Griffin; Upadhyay, Puja; Kumar, Rajan

    2016-05-01

    Flow field characteristics of a moderate aspect ratio supersonic rectangular jet were examined at two overexpanded, a perfectly expanded, and an underexpanded jet conditions. The underexpanded and one overexpanded operating condition were of maximum screech, while the second overexpanded condition was of minimum screech intensity. Streamwise particle image velocimetry was performed along both major and minor axes of the jet and the measurements were made up to 30 nozzle heights, h, where h is the small dimension of the nozzle. Select cross planes were examined using stereoscopic particle image velocimetry to investigate the jet development and the role streamwise vortices play in jet spreading at each operating condition. The results show that streamwise vortices present at the nozzle corners along with vortices excited by screech tones play a major role in the jet evolution. All cases except for the perfectly expanded operating condition exhibited axis switching at streamwise locations ranging from 11 to 16 nozzle heights downstream of the exit. The overexpanded condition of maximum screech showed the most upstream switch over, while the underexpanded case showed the farthest downstream. Both of the maximum screeching cases developed into a diamond cross-sectional profile far downstream of the exit, while the ideally expanded case maintained a rectangular shape. The overexpanded minimum screeching case eventually decayed into an oblong profile.

  14. Identifying non-normal and lognormal characteristics of temperature, mixing ratio, surface pressure, and wind for data assimilation systems

    NASA Astrophysics Data System (ADS)

    Kliewer, A. J.; Fletcher, S. J.; Jones, A. S.; Forsythe, J. M.

    2015-09-01

    Data assimilation systems and retrieval systems that are based upon a maximum likelihood estimation, many of which are in operational use, rely on the assumption that all of the errors and variables involved follow a normal distribution. This work develops a series of statistical tests to show that mixing ratio, temperature, wind and surface pressure follow non-normal, or in fact, lognormal distributions thus impacting the design-basis of many operational data assimilation and retrieval systems. For this study one year of Global Forecast System 00:00 UTC 6 h forecast were analyzed using statistical hypothesis tests. The motivation of this work is to identify the need to resolve whether or not the assumption of normality is valid and to give guidance for where and when a data assimilation system or a retrieval system needs to adapt its cost function to the mixed normal-lognormal distribution-based Bayesian model. The statistical methods of detection are based upon Shapiro-Wilk, Jarque-Bera and a χ2 test, and a new composite indicator using all three measures. Another method of detection fits distributions to the temporal-based histograms of temperature, mixing ratio, and wind. The conclusion of this work is that there are persistent areas, times, and vertical levels where the normal assumption is not valid, and that the lognormal distribution-based Bayesian model is observationally justified to minimize the error for these conditions. The results herein suggest that comprehensive statistical climatologies may need to be developed to capture the non-normal traits of the 6 h forecast.

  15. Secondary organic aerosol formation during June 2010 in Central Europe: measurements and modelling studies with a mixed thermodynamic-kinetic approach

    NASA Astrophysics Data System (ADS)

    Langmann, B.; Sellegri, K.; Freney, E.

    2014-04-01

    Until recently secondary organic carbon aerosol (SOA) mass concentrations have been systematically underestimated by three-dimensional atmospheric-chemistry-aerosol models. With a newly proposed concept of aging of organic vapours, more realistic model results for organic carbon aerosol mass concentrations can be achieved. Applying a mixed thermodynamic-kinetic approach for SOA formation shifted the aerosol size distribution towards particles in the cloud condensation nuclei size range, thereby emphasising the importance of SOA formation schemes for modelling realistic cloud and precipitation formation. The additional importance of hetero-molecular nucleation between H2SO4 and organic vapours remains to be evaluated in three-dimensional atmospheric-chemistry-aerosol models. Here a case study is presented focusing on Puy-de-Dôme, France in June 2010. The measurements indicate a considerable increase in SOA mass concentration during the measurement campaign, which could be reproduced by modelling using a simplified thermodynamic-kinetic approach for SOA formation and increased biogenic volatile organic compound (VOC) precursor emissions. Comparison with a thermodynamic SOA formation approach shows a huge improvement in modelled SOA mass concentration with the thermodynamic-kinetic approach for SOA formation. SOA mass concentration increases by a factor of up to 6 accompanied by a slight improvement of modelled particle size distribution. Even though nucleation events at Puy-de-Dôme were rare during the chosen period of investigation, a weak event in the boundary layer could be reproduced by the model in a sensitivity study when nucleation of low-volatile secondary organic vapour is included. Differences in the model results with and without nucleation of organic vapour are visible in the lower free troposphere over several days. Taking into account the nucleation of organic vapour leads to an increase in accumulation mode particles due to coagulation and

  16. Solutions Network Formulation Report. Aerosol Polarimetry Sensor Measurements of Diffuse-to-Global Irradiance Ratio for Improved Forecasting of Plant Productivity and Health

    NASA Technical Reports Server (NTRS)

    Knowlton, Kelly; Andrews, Jane C.; Ryan, Robert E.

    2007-01-01

    Studies have shown that vegetation is directly sensitive to changes in the diffuse-to-global irradiance ratio and that increased percentage of diffuse irradiation can accelerate photosynthesis. Therefore, measurements of diffuse versus global irradiance could be useful for monitoring crop productivity and overall vegetative health as they relate to the total amount of particulates in the air that result from natural disasters or anthropogenic (manmade) causes. While the components of solar irradiance are measured by satellite and surface sensors and calculated with atmospheric models, disagreement exists between the results, creating a need for more accurate and comprehensive retrievals of atmospheric aerosol parameters. Two satellite sensors--APS and VIIRS--show promise for retrieving aerosol properties at an unprecedented level of accuracy. APS is expected to be launched in December 2008. The planned launch date for VIIRS onboard NPP is September 2009. Identified partners include the USDA s ARS, North Carolina State University, Purdue Climate Change Research Center, and the Cooperative Institute for Research in the Atmosphere at Colorado State University. Although at present no formal DSSs (decision support systems) require accurate values of diffuse-to-global irradiance, this parameter is sufficiently important that models are being developed that will incorporate these measurements. This candidate solution is aligned with the Agricultural Efficiency and Air Quality National Applications.

  17. [Study of the effect of light source stability on the signal to noise ratio in degenerate four wave mixing experiment].

    PubMed

    Wang, Wei-Bo; Chen, De-Ying; Fan, Rong-Wei; Xia, Yuan-Qin

    2010-02-01

    The effects of the stability of dye laser on the signal to noise ratio in degenerate four-wave mixing (DFWM) were first investigated in iodine vapor using forward geometries. Frequency-doubled outputs from a multi-mode Nd : YAG laser pumped dye laser with laser dye PM580 dissolved in ethanol was used. With the help of forward compensated beam-split technique and imaging detecting system, the saturation intensity of DFWM spectrum in the iodine vapor at 5 554.013 nm was first measured to be 290 microJ under the condition of atmospheric pressure and room temperature. The features of the dye laser such as wavelength ranges, beam quality and energy conversion efficiency decreased gradually with increasing pumping service use, pulse number and intensity. Additionally, with the comparison of the stable and unstable dye laser output, it was found that the instability of dye laser output had greatly influenced the DFWM signal and decreased the signal to background noise ratio. Shot to shot jitter and the broadening in the output frequency leads to an effective broadening of the recorded spectrum and loss of the DFWM signal to noise ratio under the same pumping intensity at different time. The study is of importance to the detection of trace atom, molecule and radical in combustion diagnosis.

  18. Characterization of a deep-level compensation ratio through picosecond four-wave mixing on a transient reflection grating

    NASA Astrophysics Data System (ADS)

    Kadys, A.; Delaye, Ph; Roosen, G.; Jarasiunas, K.

    2007-09-01

    We demonstrate a novel application of a time-resolved four-wave mixing technique for the determination of a deep-level compensation ratio in a semi-insulating crystal. The approach is based on photoexcitation of carriers from deep impurity levels, formation of a space-charge electric field in deep traps, and monitoring dynamics of photorefractive, free- carrier and absorption gratings by light diffraction. The analysis of anisotropic diffraction features on the reflection grating provided requirements for crystal orientation in order to discriminate contribution of amplitude grating from the photorefractive phase grating, both being related to deep-trap occupation. Contributions of these optical nonlinearities were studied experimentally in (0 0 1)-oriented GaAs wafers by using a transient reflection grating configuration with a very small grating period (150 nm). Comparison of the reflection grating picosecond kinetics and its diffraction efficiency with modeling curves allowed us to ascribe the slow decay component to amplitude grating in recharged deep traps and determine their compensation ratio. The proposed technique allowed the determination of the compensation ratio of a deep EL2 donor, equal to 0.6 ± 0.05 in the given GaAs crystal.

  19. Water soluble organic carbon in aerosols (PM1, PM2.5, PM10) and various precipitation forms (rain, snow, mixed) over the southern Baltic Sea station.

    PubMed

    Witkowska, Agnieszka; Lewandowska, Anita U

    2016-12-15

    In the urbanized coastal zone of the Southern Baltic, complex measurements of water soluble organic carbon (WSOC) were conducted between 2012 and 2015, involving atmospheric precipitation in its various forms (rain, snow, mixed) and PM1, PM2.5 and PM10 aerosols. WSOC constituted about 60% of the organic carbon mass in aerosols of various sizes. The average concentration of WSOC was equal to 2.6μg∙m(-3) in PM1, 3.6μg∙m(-3) in PM2.5 and 4.4μg∙m(-3) in PM10. The lowest concentration of WSOC was noted in summer as a result of effective removal of this compound with rainfall. The highest WSOC concentrations in PM2.5 and PM10 aerosols were measured in spring, which should be associated with developing vegetation on land and in the sea. On the other hand, the highest WSOC concentrations in PM1 occurred in winter at low air temperatures and greatest atmospheric stability, when there were increased carbon emissions from fuel combustion in the communal-utility sector and from transportation. WSOC concentrations in precipitation were determined by its form. Mixed precipitation turned out to be the richest in soluble organic carbon (5.1mg·dm(-3)), while snow contained the least WSOC (1.7mg·dm(-3)). Snow and rain cleaned carbon compounds from the atmosphere more effectively when precipitation lasted longer than 24h, while in the case of mixed precipitation WSOC was removed most effectively within the first 24h.

  20. Abundance of fluorescent biological aerosol particles at temperatures conducive to the formation of mixed-phase and cirrus clouds

    SciTech Connect

    Twohy, Cynthia H.; McMeeking, Gavin R.; DeMott, Paul J.; McCluskey, Christina S.; Hill, Thomas C. J.; Burrows, Susannah M.; Kulkarni, Gourihar R.; Tanarhte, Meryem; Kafle, Durga N.; Toohey, Darin W.

    2016-01-01

    Some types of biological particles are known to nucleate ice at warmer temperatures than mineral dust, with the potential to influence cloud microphysical properties and climate. However, the prevalence of these particle types above the atmospheric boundary layer is not well known. Many types of biological particles fluoresce when exposed to ultraviolet light, and the Wideband Integrated Bioaerosol Sensor takes advantage of this characteristic to perform real-time measurements of fluorescent biological aerosol particles (FBAPs). This instrument was flown on the National Center for Atmospheric Research Gulfstream V aircraft to measure concentrations of fluorescent biological particles from different potential sources and at various altitudes over the US western plains in early autumn. Clear-air number concentrations of FBAPs between 0.8 and 12 µm diameter usually decreased with height and generally were about 10–100 L-1 in the continental boundary layer but always much lower at temperatures colder than 255 K in the free troposphere. At intermediate temperatures where biological ice-nucleating particles may influence mixed-phase cloud formation (255 K ≤ T ≤ 270 K), concentrations of fluorescent particles were the most variable and were occasionally near boundary-layer concentrations. Predicted vertical distributions of ice-nucleating particle concentrations based on FBAP measurements in this temperature regime sometimes reached typical concentrations of primary ice in clouds but were often much lower. If convection was assumed to lift boundary-layer FBAPs without losses to the free troposphere, better agreement between predicted ice-nucleating particle concentrations and typical ice crystal concentrations was achieved. Ice-nucleating particle concentrations were also measured during one flight and showed a decrease with height, and concentrations were consistent with a relationship to FBAPs established previously at the forested surface

  1. Nickel, manganese and copper removal by a mixed consortium of sulfate reducing bacteria at a high COD/sulfate ratio.

    PubMed

    Barbosa, L P; Costa, P F; Bertolino, S M; Silva, J C C; Guerra-Sá, R; Leão, V A; Teixeira, M C

    2014-08-01

    The use of sulfate-reducing bacteria (SRB) in passive treatments of acidic effluents containing heavy metals has become an attractive alternative biotechnology. Treatment efficiency may be linked with the effluent conditions (pH and metal concentration) and also to the amount and nature of the organic substrate. Variations on organic substrate and sulfate ratios clearly interfere with the biological removal of this ion by mixed cultures of SRB. This study aimed to cultivate a mixed culture of SRB using different lactate concentrations at pH 7.0 in the presence of Ni, Mn and Cu. The highest sulfate removal efficiency obtained was 98 %, at a COD/sulfate ratio of 2.0. The organic acid analyses indicated an acetate accumulation as a consequence of lactate degradation. Different concentrations of metals were added to the system at neutral pH conditions. Cell proliferation and sulfate consumption in the presence of nickel (4, 20 and 50 mg l(-1)), manganese (1.5, 10 and 25 mg l(-1)) and copper (1.5, 10 and 25 mg l(-1)) were measured. The presence of metals interfered in the sulfate biological removal however the concentration of sulfide produced was high enough to remove over 90 % of the metals in the environment. The molecular characterization of the bacterial consortium based on dsrB gene sequencing indicated the presence of Desulfovibrio desulfuricans, Desulfomonas pigra and Desulfobulbus sp. The results here presented indicate that this SRB culture may be employed for mine effluent bioremediation due to its potential for removing sulfate and metals, simultaneously.

  2. Mixing ratios and eddy covariance flux measurements of volatile organic compounds from an urban canopy (Manchester, UK)

    NASA Astrophysics Data System (ADS)

    Langford, B.; Davison, B.; Nemitz, E.; Hewitt, C. N.

    2009-03-01

    Mixing ratios and fluxes of six selected volatile organic compounds (VOCs) were measured above the city of Manchester (UK) during the summer of 2006. A proton transfer reaction-mass spectrometer was used for the measurement of mixing ratios, and fluxes were calculated from these using both the disjunct and the virtual disjunct eddy covariance techniques. The two flux systems, which operated in alternate half hours, showed good agreement, with R2 values ranging between 0.74 and 0.9 for the individual analytes. On average, fluxes measured in the disjunct mode were approximately 20% lower than those measured in the virtual mode. This difference is due to both the dampening of the VOC signal by the disjunct flux sampler and carry over from one sample to the next. Correcting for these effects reduced the difference to less than 7%. Observed fluxes are thought to be largely controlled by anthropogenic sources, with vehicle emissions the major contributor. However, both evaporative and biogenic emissions may account for some of the VOCs present. Concentrations and fluxes of the oxygenated compounds were highest on average, ranging between 0.15 to 1 mg m-2 h-1; the fluxes of aromatic compounds were lower, between 0.12 to 0.28 mg m-2 h-1. The observed fluxes were up-scaled to give city wide emission estimates for each compound and the results compared to estimates made by the National Atmospheric Emission Inventory (NAEI) for the same flux footprint. Fluxes of toluene and benzene compared most closely differing by approximately 50%, while in contrast the oxygenated fluxes were found to be between 3.6-6.3 times larger than the annual average predicted by the NAEI.

  3. Acid Mine Drainage Passive Remediation: Potential Use of Alkaline Clay, Optimal Mixing Ratio and Long Term Impacts

    NASA Astrophysics Data System (ADS)

    Plaza, F.; Liang, X.; Wen, Y.; Perone, H.

    2015-12-01

    Acid mine drainage (AMD) is one of the most adverse environmental problems of the mine industry. Surface water and ground water affected by this pollution are characterized by their acidity and the high content of sulfates and heavy metals. In this study, alkaline clay, an industrial waste with a high pH, which is utilized in the alumina refining process, was used as the remediation material to inhibit pyrite oxidation. Through a series of batch and column experiments, complemented with field measurements and geochemical modeling, three important issues associated with this passive and auto sustainable acid mine drainage remediation method were investigated: 1) the potential use of alkaline clay as an AMD remediation material, 2) the adequate alkaline clay/coal refuse mixing ratio (AC/CR) to ensure pH values near to neutral conditions, and, 3) the prediction of long term impacts, in terms of the trends of the main parameters involved in this process such as pH, concentrations of sulfate, iron and other dissolved contaminants. Both field measurements and the samples used for the experiments came from a coal waste site located in Mather, Pennsylvania. Alkaline clay proved to be an effective remediation material for AMD. It was found that 10% AC/CR is an adequate mixing ratio (i.e. the upper limit), which has been also indicated by field measurements. The concentrations of some contaminants such as iron, manganese or sulfate are significantly reduced with the remediation approach, compared to those representative concentrations found in mine tailings. Moreover, results suggest a very reliable long-term stability of the remediation (i.e. neutral pH conditions are maintained), thus enhancing the generation of iron precipitates that could produce pyrite grain coating and hardpan (i.e. cemented layer) on the surface. These processes also made the amended layer less porous, thus increasing water retention and hindering oxygen diffusion.

  4. Emission ratio of carbonaceous aerosols observed near crop residual burning sources in a rural area of the Yangtze River Delta Region, China

    NASA Astrophysics Data System (ADS)

    Pan, X. L.; Kanaya, Y.; Wang, Z. F.; Taketani, F.; Tanimoto, H.; Irie, H.; Takashima, H.; Inomata, S.

    2012-11-01

    Intensive open crop residue burning (OCRB) has a great impact on regional air quality and climate. A field observation campaign in a rural area of the Yangtze River Delta Region (YRDR) was performed during the harvest season, and Elemental carbon (ECa), organic carbon (OC), black carbon (BCe), carbon monoxide (CO), carbon dioxide (CO2) and PM2.5mass were concurrently measured. During the observation period, urban pollution and OCRB-impact episodes were classified. The emission ratio of ECa mass (defined as the ΔECa/ΔCO ratio) from OCRB was estimated to be 18.2 ± 4.6 ng/m3/ppbv, much higher than that (3.0 ± 0.3 ng/m3/ppbv) of urban pollution from the YRDR. A significant amount of OC was emitted from OCRB with ΔOC/ΔCO ratio of 101.3 ± 41.6 ng/m3/ppbv. The value found in the present study was near the upper limit of OC emission ratios in the literature, implying great impacts from combustion conditions, types of biomass burned and subsequent evolution. Regarding urban pollution episodes, the ΔOC/ΔCO ratio was found to be 23.7 ± 2.4 ng/m3/ppbv, and secondary organics accounted for the major fraction of OC mass. Combustions phases of OCRB were classified according to a modified combustion efficiency (MCE, defined as ΔCO2/(ΔCO + ΔCO2)). Our results support the view that ECa tend to be produced in flaming combustions (MCE > 0.95) than in smoldering combustions (MCE < 0.95), whereas OC is emitted preferentially from smoldering combustions. Based on our observed carbonaceous aerosol correlations, we estimate that the ECa and OC emissions from OCRB in East Asia might be underestimated by at least 50%.

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

    NASA Astrophysics Data System (ADS)

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

    2016-09-01

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

  6. Mixing state and sources of submicron regional background aerosols in the northern Qinghai-Tibet Plateau and the influence of biomass burning

    NASA Astrophysics Data System (ADS)

    Li, W. J.; Chen, S. R.; Xu, Y. S.; Guo, X. C.; Sun, Y. L.; Yang, X. Y.; Wang, Z. F.; Zhao, X. D.; Chen, J. M.; Wang, W. X.

    2015-12-01

    Transmission electron microscopy (TEM) was employed to obtain morphology, size, composition, and mixing state of background aerosols with diameter less than 1 μm in the northern Qinghai-Tibet Plateau (QTP) during 15 September to 15 October 2013. Individual aerosol particles mainly contained secondary inorganic aerosols (SIA - sulfate and nitrate) and organics during clean periods (PM2.5 mass concentration less than 2.5 μg m-3). The presence of K-Na-Cl associated with organics and an increase in soot particles suggest that an intense biomass burning event caused the highest PM2.5 concentrations (> 30 μg m-3) during the study. A large number fraction of the fly-ash-containing particles (21.73 %) suggests that coal combustion emissions in the QTP significantly contributed to air pollutants at the medium pollution level (PM2.5: 10-30 μg m-3). We concluded that emissions from biomass burning and from coal combustion both constantly contribute to anthropogenic particles in the QTP atmosphere. Based on size distributions of individual particles at different pollution levels, we found that gas condensation on existing particles is an important chemical process for the formation of SIA with organic coating. TEM observations show that refractory aerosols (e.g., soot, fly ash, and visible organic particles) likely adhere to the surface of SIA particles larger than 200 nm due to coagulation. Organic coating and soot on surface of the aged particles likely influence their hygroscopic and optical properties, respectively, in the QTP. To our knowledge, this study reports the first microscopic analysis of fine particles in the background QTP air.

  7. Assessing Aerosol Mixed Layer Heights from the NASA Larc Airborne High Spectral Resolution Lidar (HSRL) during the Discover-AQ Field Campaigns

    NASA Astrophysics Data System (ADS)

    Scarino, A. J.; Ferrare, R. A.; Burton, S. P.; Hostetler, C. A.; Hair, J. W.; Rogers, R. R.; Berkoff, T.; Sawamura, P.; Collins, J. E., Jr.; Seaman, S. T.; Cook, A. L.; Harper, D. B.; Follette-Cook, M. B.; daSilva, A.; Randles, C. A.

    2014-12-01

    The first- and second-generation NASA airborne High Spectral Resolution Lidars (HSRL-1 and HSRL-2) have been deployed on board the NASA Langley Research Center King Air aircraft during the Deriving Information on Surface Conditions from Column and VERtically Resolved Observations Relevant to Air Quality (DISCOVER-AQ) field campaigns. These included deployments during July 2011 over Washington, D.C. and Baltimore, MD, during January and February 2013 over the San Joaquin Valley of California, during September 2013 over Houston, TX and during July and August 2014 over Denver, CO. Measurements of aerosol extinction, backscatter, and depolarization are available from both HSRL-1 and HSRL-2 in coordination with other participating research aircraft and ground sites. These measurements constitute a diverse data set for use in characterizing the spatial and temporal distribution of aerosols, aerosol optical thickness (AOT), as well as the mixed layer (ML) height. Analysis of the ML height at these four locations is presented, including temporal and horizontal variability and comparisons between land and water, including the Chesapeake Bay and Galveston Bay. Using the ML heights, the distribution of AOT relative to the ML heights is determined, which is relevant for assessing the long-range transport of aerosols. The ML heights are also used to help relate column AOT measurements and extinction profiles to surface PM2.5 concentrations. The HSRL ML heights are also used to evaluate the performance in simulating the temporal and spatial variability of ML heights from both chemical regional models and global forecast models.

  8. Quasi-biennial oscillation of the tropical stratospheric aerosol layer

    NASA Astrophysics Data System (ADS)

    Hommel, R.; Timmreck, C.; Giorgetta, M. A.; Graf, H. F.

    2015-05-01

    This study describes how aerosol in an aerosol-coupled climate model of the middle atmosphere is influenced by the quasi-biennial oscillation (QBO) during times when the stratosphere is largely unperturbed by volcanic material. In accordance with satellite observations, the vertical extent of the stratospheric aerosol layer in the tropics is modulated by the QBO by up to 6 km, or ~ 35% of its mean vertical extent between 100-7 hPa (about 16-33 km). Its largest vertical extent lags behind the occurrence of strongest QBO westerlies. The largest reduction lags behind maximum QBO easterlies. Strongest QBO signals in the aerosol surface area (30 %) and number densities (up to 100% e.g. in the Aitken mode) are found in regions where aerosol evaporates, that is above the 10 hPa pressure level (~ 31 km). Positive modulations are found in the QBO easterly shear, negative modulations in the westerly shear. Below 10 hPa, in regions where the aerosol mixing ratio is largest (50-20 hPa, or ~ 20-26 km), in most of the analysed parameters only moderate statistically significant QBO signatures (< 10%) have been found. QBO signatures in the model prognostic aerosol mixing ratio are significant at the 95% confidence level throughout the tropical stratosphere where modelled mixing ratios exceed 0.1 ppbm. In some regions of the tropical lower stratosphere the QBO signatures in other analysed parameters are partly not statistically significant. Peak-to-peak amplitudes of the QBO signature in the prognostic mixing ratios are up to twice as large as seasonal variations in the region where aerosols evaporate and between 70-30 hPa. Between the tropical tropopause and 70 hPa the QBO signature is relatively weak and seasonal variations dominate the variability of the simulated Junge layer. QBO effects on the upper lid of the tropical aerosol layer turn the quasi-static balance between processes maintaining the layer's vertical extent into a cyclic balance when considering this dominant mode

  9. Nutritive value of mixed proteins. 2. As determined by net protein utilization and protein efficiency ratio tests.

    PubMed

    Woodham, A A; Clarke, E M

    1977-05-01

    1. A fish meal, meat meal, soya-bean meal, groundnut meal and sunflower-seed meal of known amino acid composition were evaluated individually, and combined in all possible pairs, by the estimation of net protein utilization (NPU) and protein efficiency ratio (body-weight gain: crude protein intake; PER) using rats. Each pair provided a total of 100 g protein/kg diet made up so that the amounts of the constituents were (w/w) 100:0, 80:20, 60:40, 20:80, and 0:100. 2. Marked synergistic effects were noted only for mixtures of sunflower-seed meal with soya-bean, fish and meat meals. 3. Chemical score ([amount of limiting amino acid/the rat's requirement for the same amino acid] X100; CS), but not essential amino acid index; geometric mean for the ratio, amount of essential amino acid: the rat's requirement for that amino acid, for all ten essential amino acids; EAAI), successfully predicted the rankings of all mixtures except groundnut meal-meat meal and groundnut meal-soya-bean meal, by both PER and NPU tests. 4. Although there is broad agreement linking results of PER and NPU tests with results obtained by a more practical feeding trial in which the mixtures were evaluated as supplements to cereals, neither of these two standard tests is capable of predicting in every instance the advantages to be gained by mixing protein concentrates.

  10. On the implications of aerosol liquid water and phase separation for organic aerosol mass

    NASA Astrophysics Data System (ADS)

    Pye, Havala O. T.; Murphy, Benjamin N.; Xu, Lu; Ng, Nga L.; Carlton, Annmarie G.; Guo, Hongyu; Weber, Rodney; Vasilakos, Petros; Wyat Appel, K.; Hapsari Budisulistiorini, Sri; Surratt, Jason D.; Nenes, Athanasios; Hu, Weiwei; Jimenez, Jose L.; Isaacman-VanWertz, Gabriel; Misztal, Pawel K.; Goldstein, Allen H.

    2017-01-01

    Organic compounds and liquid water are major aerosol constituents in the southeast United States (SE US). Water associated with inorganic constituents (inorganic water) can contribute to the partitioning medium for organic aerosol when relative humidities or organic matter to organic carbon (OM / OC) ratios are high such that separation relative humidities (SRH) are below the ambient relative humidity (RH). As OM / OC ratios in the SE US are often between 1.8 and 2.2, organic aerosol experiences both mixing with inorganic water and separation from it. Regional chemical transport model simulations including inorganic water (but excluding water uptake by organic compounds) in the partitioning medium for secondary organic aerosol (SOA) when RH > SRH led to increased SOA concentrations, particularly at night. Water uptake to the organic phase resulted in even greater SOA concentrations as a result of a positive feedback in which water uptake increased SOA, which further increased aerosol water and organic aerosol. Aerosol properties, such as the OM / OC and hygroscopicity parameter (κorg), were captured well by the model compared with measurements during the Southern Oxidant and Aerosol Study (SOAS) 2013. Organic nitrates from monoterpene oxidation were predicted to be the least water-soluble semivolatile species in the model, but most biogenically derived semivolatile species in the Community Multiscale Air Quality (CMAQ) model were highly water soluble and expected to contribute to water-soluble organic carbon (WSOC). Organic aerosol and SOA precursors were abundant at night, but additional improvements in daytime organic aerosol are needed to close the model-measurement gap. When taking into account deviations from ideality, including both inorganic (when RH > SRH) and organic water in the organic partitioning medium reduced the mean bias in SOA for routine monitoring networks and improved model performance compared to observations from SOAS. Property updates from

  11. Cloud Forming Potential of Aminium Carboxylate Aerosols

    NASA Astrophysics Data System (ADS)

    Gomez Hernandez, M. E.; McKeown, M.; Taylor, N.; Collins, D. R.; Lavi, A.; Rudich, Y.; Zhang, R.

    2014-12-01

    Atmospheric aerosols affect visibility, air quality, human health, climate, and in particular the aerosol direct and indirect forcings represent the largest uncertainty in climate projections. In this paper, we present laboratory measurements of the hygroscopic growth factors (HGf) and cloud condensation nuclei (CCN) activity of a series of aminium carboxylate salt aerosols, utilizing a Hygroscopicity Tandem Differential Mobility Analyzer (HTDMA) coupled to a Condensation Particle Counter (CPC) and a CCN counter. HGf measurements were conducted for size-selected aerosols with diameters ranging from 46 nm to 151 nm and at relative humidity (RH%) values ranging from 10 to 90%. In addition, we have calculated the CCN activation diameters for the aminium carboxylate aerosols and derived the hygroscopicity parameter (k or kappa) values for all species using three methods, i.e., the mixing rule approximation, HGf, and CCN results. Our results show that variations in the ratio of acid to base directly affect the activation diameter, HGf, and (k) values of the aminium carboxylate aerosols. Atmospheric implications of the variations in the chemical composition of aminium carboxylate aerosols on their cloud forming potential will be discussed.

  12. Isotopic ratios of nitrate in aerosol samples from Mt. Lulin, a high-altitude station in Central Taiwan

    NASA Astrophysics Data System (ADS)

    Guha, Tania; Lin, C. T.; Bhattacharya, S. K.; Mahajan, A. S.; Ou-Yang, Chang-Feng; Lan, Yi-Ping; Hsu, S. C.; Liang, Mao-Chang

    2017-04-01

    The importance of Asian countries towards increase of atmospheric pollutants is being examined critically in recent times. In this context, we carried out analysis of nitrates separated from aerosol samples collected during 2010 from Mt. Lulin (NOAA code: LLN), Taiwan, located at an altitude of 2 862 m above sea level. Large temporal variations are seen in δ15N, δ18O and Δ17O values of the nitrate, with day-to-day variations comparable to the seasonal amplitude. The δ15N values of nitrate are found to be higher in spring months (March-April; -1±3‰) and lower in summer (June-September; -5±3‰). Similarly, the δ18O (69 ± 15‰ versus 32 ± 13‰) and Δ17O (23 ± 5‰ versus 12 ± 4‰) values are higher in spring and lower in summer. The lowest δ18O value observed was 10.8‰. The higher values of δ15N in spring could be attributed to enhanced contribution from fossil fuel combustions, especially burning of coal in nearby Asian countries like China, with the resultant pollutants being brought to the Lulin station by long-range transport. An alternative explanation is the isotopic exchange reaction between N2O5 and HNO3 that elevates the δ15N value in nitrate. The oxygen isotope variability is explained by changes in contribution from two major pathways of nitrate formation from its precursor NOx molecules. During spring time, nitrate formation via the N2O5 pathway is dominant, resulting in higher values of both δ18O and Δ17O. In contrast, during summer, formation involving HO2/RO2 radicals becomes important, producing lower values of δ18O and Δ17O. A chemistry box model was used to study the nitrate formation pathways through oxidation of NO and NO2 via formation of NO2 and NO3-/HNO3. Both the model results and observations suggest that for the formation of NO2 from NO, the pathway via O3 is more active in spring, whereas in summer the pathway via HO2/RO2 radicals predominates. For the subsequent formation of NO3- and HNO3, the OH pathway is more

  13. Effects of strain rate, mixing ratio, and stress-strain definition on the mechanical behavior of the polydimethylsiloxane (PDMS) material as related to its biological applications.

    PubMed

    Khanafer, Khalil; Duprey, Ambroise; Schlicht, Marty; Berguer, Ramon

    2009-04-01

    Tensile tests on Polydimethylsiloxane (PDMS) materials were conducted to illustrate the effects of mixing ratio, definition of the stress-strain curve, and the strain rate on the elastic modulus and stress-strain curve. PDMS specimens were prepared according to the ASTM standards for elastic materials. Our results indicate that the physiological elastic modulus depends strongly on the definition of the stress-strain curve, mixing ratio, and the strain rate. For various mixing ratios and strain rates, true stress-strain definition results in higher stress and elastic modulus compared with engineering stress-strain and true stress-engineering strain definitions. The elastic modulus increases as the mixing ratio increases up-to 9:1 ratio after which the elastic modulus begins to decrease even as the mixing ratio continues to increase. The results presented in this study will be helpful to assist the design of in vitro experiments to mimic blood flow in arteries and to understand the complex interaction between blood flow and the walls of arteries using PDMS elastomer.

  14. Lead isotopes and trace metal ratios of aerosols as tracers of Pb pollution sources in Kanpur, India

    NASA Astrophysics Data System (ADS)

    Sen, Indra; Bizimis, Michael; Tripathi, Sachchida; Paul, Debajyoti; Tyagi, Swati; Sengupta, Deep

    2015-04-01

    The anthropogenic flux of Pb in the Earth's surface is almost an order of magnitude higher than its corresponding natural flux [1]. Identifying the sources and pathways of anthropogenic Pb in environment is important because Pb toxicity is known to have adverse effects on human health. Pb pollution sources for America, Europe, and China are well documented. However, sources of atmospheric Pb are unknown in India, particularly after leaded gasoline was phased out in 2000. India has a developing economy with a rapidly emerging automobile and high temperature industry, and anthropogenic Pb emission is expected to rise in the next decade. In this study, we report on the Pb- isotope compositions and trace metal ratios of airborne particulates collected in Kanpur, an industrial city in northern India. The Pb concentration in the airborne particulate matter varies between 14-216 ng/m3, while the other heavy metals vary by factor of 10 or less, e.g. Cd=0.3-3 ng/m3, As=0.4-3.5 ng/m3, Zn=36-161 ng/m3, and Cu=3-22 ng/m3. The 206Pb/207Pb, 208Pb/206Pb, and 208Pb/207Pb vary between 1.112 - 1.129, 2.123-2.141, and 2.409-2.424 respectively, and are highly correlated with each other (R2>0.9). Pb isotopes and trace metal data reveals that coal combustion is the major source of anthropogenic Pb in the atmosphere, with limited contribution from mining and smelting processes. We further conclude that combination of Pb isotope ratios and V/Pb ratios are powerful tracers for Pb source apportionment studies, which is otherwise difficult to differentiate based only on Pb systematics [1] Sen and Peucker-Ehrenbrink (2012), Environ. Sci. Technol.(46), 8601-8609

  15. Recent activities in the Aerosol Generation and Transport Program

    SciTech Connect

    Adams, R.E.

    1984-01-01

    General statements may be made on the behavior of single-component and multi-component aerosols in the Nuclear Safety Pilot Plant vessel. The removal processes for U/sub 3/O/sub 8/, Fe/sub 2/O/sub 3/, and U/sub 3/O/sub 8/ + Fe/sub 2/O/sub 3/ aerosols are enhanced in a steam-air atmosphere. Steam-air seems to have little effect on removal of concrete aerosol from the vessel atmosphere. A steam-air environment causes a change in aerosol shape from chain-agglomerate to basically spherical for U/sub 3/O/sub 8/, Fe/sub 2/O/sub 3/, and U/sub 3/O/sub 8/ + Fe/sub 2/O/sub 3/ aerosol; for concrete the change in aerosol shape is from chain-agglomerate to partially spherical. The mass ratio of the individual components of a multi-component aerosol seems to have an observable influence on the resultant behavior of these aerosols in steam. The enhanced rate of removal of the U/sub 3/O/sub 8/, the Fe/sub 2/O/sub 3/, and the mixed U/sub 3/O/sub 8/ + Fe/sub 2/O/sub 3/ aerosols from the atmosphere of the NSPP vessel by steam-air is probably caused by the change in aerosol shape and the condensation of steam on the aerosol surfaces combining to increase the effect of gravitational settling. The apparent lack of an effect by steam-air on the removal rate of concrete aerosol could result from a differing physical/chemical response of the surfaces of this aerosol to condensing steam.

  16. Quantitative Reconstruction of Sulfur Deposition Using a Mixing Model Based on Sulfur Isotope Ratios in Tree Rings.

    PubMed

    Ishida, Takuya; Tayasu, Ichiro; Takenaka, Chisato

    2015-11-01

    Quantification of sulfur (S) deposition is critical to deciphering the environmental archive of S in terrestrial ecosystems. Here we propose a mixing model that quantifies S deposition based on the S isotope ratio (δS) in tree rings. We collected samples from Japanese cedar ( D. Don) stumps from two sites: one near Yokkaichi City (YOK), which is well known for having the heaviest S air pollution in the world, and one at Inabu-cho (INA) in central Japan, which has been much less affected by air pollution. The δS profiles at both sites are consistent with S air pollution and contributions of anthropogenic S. The minimum value in YOK is lower than the δS values of anthropogenic S or any other possible source. Because the δS in the tree rings is affected by fractionation in the forest ecosystems, we used a mixing model to account for the isotope effects and to distinguish the sources of S. Based on the model results, we infer that the peak of S emissions at YOK occurred sometime between the late 1960s and early 1970s (489 mmol m yr). This estimated value is comparable with the highest reported values in Europe. This is the first quantitative estimate of anthropogenic input of S in forest systems based on δS in tree rings. Our results suggest that tree ring data can be used when monitoring stations of atmospheric S are lacking and that estimates of S deposition using δS in tree rings will advance our understanding of the local-scale S dynamics and the effect of human activities on it.

  17. Plant lighting system with five wavelength-band light-emitting diodes providing photon flux density and mixing ratio control

    PubMed Central

    2012-01-01

    Background Plant growth and development depend on the availability of light. Lighting systems therefore play crucial roles in plant studies. Recent advancements of light-emitting diode (LED) technologies provide abundant opportunities to study various plant light responses. The LED merits include solidity, longevity, small element volume, radiant flux controllability, and monochromaticity. To apply these merits in plant light response studies, a lighting system must provide precisely controlled light spectra that are useful for inducing various plant responses. Results We have developed a plant lighting system that irradiated a 0.18 m2 area with a highly uniform distribution of photon flux density (PFD). The average photosynthetic PFD (PPFD) in the irradiated area was 438 micro-mol m–2 s–1 (coefficient of variation 9.6%), which is appropriate for growing leafy vegetables. The irradiated light includes violet, blue, orange-red, red, and far-red wavelength bands created by LEDs of five types. The PFD and mixing ratio of the five wavelength-band lights are controllable using a computer and drive circuits. The phototropic response of oat coleoptiles was investigated to evaluate plant sensitivity to the light control quality of the lighting system. Oat coleoptiles irradiated for 23 h with a uniformly distributed spectral PFD (SPFD) of 1 micro-mol m–2 s–1 nm–1 at every peak wavelength (405, 460, 630, 660, and 735 nm) grew almost straight upwards. When they were irradiated with an SPFD gradient of blue light (460 nm peak wavelength), the coleoptiles showed a phototropic curvature in the direction of the greater SPFD of blue light. The greater SPFD gradient induced the greater curvature of coleoptiles. The relation between the phototropic curvature (deg) and the blue-light SPFD gradient (micro-mol m–2 s–1 nm–1 m–1) was 2 deg per 1 micro-mol m–2 s–1 nm–1 m–1. Conclusions The plant lighting system, with a computer with a graphical user interface

  18. Water, ammonia, and H 2S mixing ratios in Jupiter's five-micron hot spots: A dynamical model

    NASA Astrophysics Data System (ADS)

    Friedson, A. James

    2005-09-01

    The Galileo probe entered the jovian atmosphere at the southern edge of a 5-micron hot spot, one of typically 8-10 quasi-evenly-spaced longitudinal areas of anomalously high 5-micron IR emission that reside in a narrow latitude band centered on +7.5 degrees. These hot spots are characterized primarily by a low abundance of the cloud particles that dominate the 5-micron opacity at other locations on the planet, and by significant desiccation of ammonia, water and hydrogen sulfide in the upper layers of the troposphere. Ortiz et al. [1998. Evolution and persistence of 5-micron hot spots at the Galileo probe entry latitude. J. Geophys. Res. 103, 23,051-23,069] found that the latitude and drift rate of the hot spots could be explained if they are formed by an equatorially trapped Rossby wave of meridional degree 1 moving with a phase speed between 99 and 103 m s -1 relative to System III. Here we model additional properties of the hot spots in terms of the amplitude saturation of such a wave propagating in the weakly stratified deep troposphere. We identify the hot spots with locations where the wave plus mean thermal stratification becomes marginally stable. In these locations, potential temperature isotherms stretch downward to very deep levels in the troposphere. Since fluid parcels follow these isotherms under adiabatic flow conditions, the parcels dive downward when they enter the portion of the wave associated with the hot spot and soar upward upon leaving the spot. We show that this model can account for the anomalous vertical profiles of NH 3, H 2O, and H 2S mixing ratio measured by the Galileo probe. Pressures vary by as much as 20 bar over potential temperature isotherms in solutions that produce sufficient desiccation of water and H 2S in hot spots. Approximately 6×10 of Jupiter's internal heat flux must be tapped to maintain the wave over the mean hot spot lifetime of 10 7 s. The results suggest that the phenomenon that causes hot spots may occur widely

  19. The New England Batholith of eastern Australia: Evidence of silicic magma mixing from zircon 176 Hf/ 177 Hf ratios

    NASA Astrophysics Data System (ADS)

    Shaw, S. E.; Flood, R. H.; Pearson, N. J.

    2011-09-01

    Zircon Hf isotopic data from six granite supersuites recognised in the New England Batholith of eastern Australia indicate that magma mixing is present in all plutons. Apart from the S-type supersuites, inherited zircons are rare to absent, suggesting that initial melt temperatures were above zircon saturation for the M-, I- and A-type granites. In all supersuites, the range of zircon Hf model ages calculated relative to arc mantle varies greatly, with younger model ages somewhat less than the Permian and Triassic age of crystallisation, and older model ages indicating derivation from source rocks that may be as old as Neoproterozoic. The older model ages are consistent with late Precambrian rocks in the lower crust that may be elements of the Lachlan Fold Belt underlying the New England Fold Belt. Whole-rock δ 18O and ɛNd values, 87Sr/ 86Sr initial ratios (Sr i) and oxidation state (Fe 2O 3/FeO) are summarised for the five named supersuites, and for a previously unnamed group of Triassic plutons situated east of the main Batholith for which we propose the name Carrai supersuite. Supersuites with higher δ 18O, higher Sr i, lower δ 7Li and lower Fe 2O 3/FeO ratios indicate a metasedimentary component input. The pattern of zircon Hf isotopic variation reflects the other isotopic and geochemical indicators closely, the additional value being that it preserves a magmatic crystallisation record of Hf isotopic variation, that is, a measure of magma mixing from magma generation to final crystallisation. Using the above criteria, at least three distinct crustal components are considered necessary to explain the compositional and isotopic diversity within the Batholith. The crustal components indicated are: 1) a metasedimentary component of Carboniferous and Devonian age for the Hillgrove, Bundarra and Uralla supersuites; 2) a lower crustal K-rich (and Sr-rich) I-type component for the Moonbi, Carrai and possibly Uralla supersuites that could be as old as Proterozoic

  20. Investigating the effect of mixing ratio on molar mass distributions of synthetic polymers determined by MALDI-TOF mass spectrometry using design of experiments.

    PubMed

    Brandt, Heike; Ehmann, Thomas; Otto, Matthias

    2010-11-01

    It is well known that the mixing ratio affects the molar mass distribution of synthetic polymers determined by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS). Surely, the molar mixing ratio determines whether a mass spectrum will be obtained or not. However, depending on the mass range, several effects such as multimer formation occur, which might be a source of errors in molar mass distribution calculations. In this study, the effect of mixing ratio was investigated for several synthetic polymers, including polystyrene (PS), poly(dimethylsiloxane) (PDMS), poly(ethylene glycol) (PEG), and poly(methyl methacrylate) (PMMA) using statistical designs of experiments. The 2(3) full factorial design was found to be suitable in the study of more than 1000 samples. The obtained MALDI mass spectra as well as the ANOVA statistics show that the mixing ratio affects the molar mass distribution. The optimal mixing ratio for a defined synthetic polymer depends on the studied combination (matrix, cationization reagent, solvent).

  1. On the implications of aerosol liquid water and phase ...

    EPA Pesticide Factsheets

    Organic compounds and liquid water are major aerosol constituents in the southeast United States (SE US). Water associated with inorganic constituents (inorganic water) can contribute to the partitioning medium for organic aerosol when relative humidities or organic matter to organic carbon (OM ∕ OC) ratios are high such that separation relative humidities (SRH) are below the ambient relative humidity (RH). As OM ∕ OC ratios in the SE US are often between 1.8 and 2.2, organic aerosol experiences both mixing with inorganic water and separation from it. Regional chemical transport model simulations including inorganic water (but excluding water uptake by organic compounds) in the partitioning medium for secondary organic aerosol (SOA) when RH  >  SRH led to increased SOA concentrations, particularly at night. Water uptake to the organic phase resulted in even greater SOA concentrations as a result of a positive feedback in which water uptake increased SOA, which further increased aerosol water and organic aerosol. Aerosol properties, such as the OM ∕ OC and hygroscopicity parameter (κorg), were captured well by the model compared with measurements during the Southern Oxidant and Aerosol Study (SOAS) 2013. Organic nitrates from monoterpene oxidation were predicted to be the least water-soluble semivolatile species in the model, but most biogenically derived semivolatile species in the Community Multiscale Air Quality (CMAQ) model were hig

  2. Photodiode array to charged aerosol detector response ratio enables comprehensive quantitative monitoring of basic drugs in blood by ultra-high performance liquid chromatography.

    PubMed

    Viinamäki, Jenni; Ojanperä, Ilkka

    2015-03-20

    Quantitative screening for a broad range of drugs in blood is regularly required to assess drug abuse and poisoning within analytical toxicology. Mass spectrometry-based procedures suffer from the large amount of work required to maintain quantitative calibration in extensive multi-compound methods. In this study, a quantitative drug screening method for blood samples was developed based on ultra-high performance liquid chromatography with two consecutive detectors: a photodiode array detector and a corona charged aerosol detector (UHPLC-DAD-CAD). The 2.1 mm × 150 mm UHPLC column contained a high-strength silica C18 bonded phase material with a particle size of 1.8 μm, and the mobile phase consisted of methanol/0.1% trifluoroacetic acid in gradient mode. Identification was based on retention time, UV spectrum and the response ratio from the two detectors. Using historic calibration over a one-month period, the median precision (RSD) of retention times was 0.04% and the median accuracy (bias) of quantification 6.75%. The median precision of the detector response ratio over two orders of magnitude was 12%. The applicable linear ranges were generally 0.05-5 mg L(-1). The method was validated for 161 compounds, including antipsychotics, antidepressants, antihistamines, opioid analgesics, and adrenergic beta blocking drugs, among others. The main novelty of the method was the proven utility of the response ratio of DAD to CAD, which provided the additional identification efficiency required. Unlike with mass spectrometry, the high stability of identification and quantification allowed the use of facile historic calibration.

  3. Comparative Analysis of Alternative Spectral Bands of CO2 and O2 for the Sensing of CO2 Mixing Ratios

    NASA Technical Reports Server (NTRS)

    Pliutau, Denis; Prasad, Narasimha S.

    2013-01-01

    We performed comparative studies to establish favorable spectral regions and measurement wavelength combinations in alternative bands of CO2 and O2, for the sensing of CO2 mixing ratios (XCO2) in missions such as ASCENDS. The analysis employed several simulation approaches including separate layers calculations based on pre-analyzed atmospheric data from the modern-era retrospective analysis for research and applications (MERRA), and the line-byline radiative transfer model (LBLRTM) to obtain achievable accuracy estimates as a function of altitude and for the total path over an annual span of variations in atmospheric parameters. Separate layer error estimates also allowed investigation of the uncertainties in the weighting functions at varying altitudes and atmospheric conditions. The parameters influencing the measurement accuracy were analyzed independently and included temperature sensitivity, water vapor interferences, selection of favorable weighting functions, excitations wavelength stabilities and other factors. The results were used to identify favorable spectral regions and combinations of on / off line wavelengths leading to reductions in interferences and the improved total accuracy.

  4. Purple Crow Lidar Vibrational Raman water vapor mixing ratio and temperature measurements in the Upper Troposphere and Lower Stratosphere

    NASA Astrophysics Data System (ADS)

    Sica, R. J.; Argall, P. S.

    2006-12-01

    Purple Crow Lidar (PCL) measurements of the vibrational Raman-shifted backscatter from water vapor and nitrogen molecules allows height profiles of water vapor mixing ratio to be measured from 500 m to up into the lower stratosphere from the Delaware Observatory near London, Canada. In addition, the Raman nitrogen measurements allow the determination of temperature profiles from about 10 km to 40 km altitude. External calibration of these measurements is necessary to compensate for instrumental effects, uncertainties in our knowledge of the relevant molecular cross sections, and atmospheric transmission. A comparison of the PCL derived water vapor concentration and temperature profiles with routine radiosonde measurements from Detroit and Buffalo on 37 and 141 nights respectively, was undertaken to provide this calibration, which showed mean temperature differences over all flights for altitudes above 9 km of about 0.5 K, with agreement for water vapor below 7 km to within ±12%. Comparisons of the cold point temperature with the coincident water vapor measurements will be presented to investigate the transport of air from the tropics to midlatitudes.

  5. First Look at the Upper Tropospheric Ozone Mixing Ratio from OMI Estimated using the Cloud Slicing Technique

    NASA Technical Reports Server (NTRS)

    Bhartia, Pawan K.; Ziemke, Jerry; Chandra, Sushil; Joiner, Joanna; Vassilkov, Alexandra; Taylor, Steven; Yang, Kai; Ahn, Chang-Woo

    2004-01-01

    The Cloud Slicing technique has emerged as a powerful tool for the study of ozone in the upper troposphere. In this technique one looks at the variation with cloud height of the above-cloud column ozone derived from the backscattered ultraviolet instruments, such as TOMS, to determine the ozone mixing ratio. For this technique to work properly one needs an instrument with relatively good horizontal resolution with very good signal to noise in measuring above-cloud column ozone. In addition, one needs the (radiatively) effective cloud pressure rather than the cloud-top pressure, for the ultraviolet photons received by a satellite instrument are scattered from inside the cloud rather than from the top. For this study we use data from the OMI sensor, which was recently launched on the EOS Aura satellite. OMI is a W-Visible backscattering instrument with a nadir pixel size of 13 x 24 km. The effective cloud pressure is derived from a new algorithm based on Rotational Raman Scattering and O2-O2, absorption in the 340-400 nm band of OMI.

  6. Remote sensing measurements of the CO2 mixing ratio in the planetary boundary layer using cloud slicing with airborne lidar

    NASA Astrophysics Data System (ADS)

    Ramanathan, Anand K.; Mao, Jianping; Abshire, James B.; Allan, Graham R.

    2015-03-01

    We have measured the CO2 volume mixing ratio (VMR) within the planetary boundary layer (PBL) using cloud slicing with an airborne pulsed integrated path differential absorption (IPDA) lidar from flight altitudes of up to 13 km. During a flight over Iowa in summer 2011, simultaneous measurement of the optical range and CO2 absorption to clouds and the ground were made using time-resolved detection of pulse echoes from each scattering surface. We determined the CO2 absorption in the PBL by differencing the two lidar-measured absorption line shapes, one to a broken shallow cumulus cloud layer located at the top of the PBL and the other to the ground. Solving for the CO2 VMR in the PBL and that of the free troposphere, we measured a ≈15 ppm (4%) drawdown in the PBL. Both CO2 VMRs were within ≈3 ppm of in situ CO2 profile measurements. We have also demonstrated cloud slicing using scatter from thin, diffuse cirrus clouds and cumulus clouds, which allowed solving for the CO2 VMR for three vertical layers. The technique and retrieval algorithm are applicable to a space-based lidar instrument as well as to lidar IPDA measurements of other trace gases. Thus, lidar cloud slicing also offers promise toward space-based remote sensing of vertical trace gas profiles in the atmosphere using a variety of clouds.

  7. Dependence of Ice Formation in Sierra Winter Orographic Clouds on the Mixing State of Aerosols Serving as Ice Nuclei

    NASA Astrophysics Data System (ADS)

    DeMott, P. J.; Prather, K. A.; Sullivan, R. C.; Suski, K.; Comstock, J. M.; Tomlinson, J. M.; Rosenfeld, D.; Prenni, A. J.; Cazorla, A.

    2011-12-01

    The CalWater study of February to March 2011 offered the opportunity for observations of aerosols from local, regional and long distance sources as they were integrated into clouds and precipitation in the Sierra Nevada. Single particle chemical analysis of cloud particle residual nuclei and surface precipitation, and their association with changes in cloud microphysical differences, suggest that ice initiation and precipitation formation were strongly affected by intrusions of Asian dust. This is consistent with coincident processing of aerosols present in ambient air and cloud particle residuals as ice nuclei. Elevated ice nuclei concentrations were associated with the presence of dust detected in cloud particle residuals, and dust particles dominated ice nuclei chemical compositions assessed by transmission electron microscopy x-ray analyses at these same times. Evidence of the role of Asian dust as ice nuclei during 2011 are consistent with back trajectory analyses and with recently published observational findings from CalWater Early Start data from 2009. The relative roles of aerosols from the marine boundary layer, biomass burning, and pollution as ice nuclei will also be discussed.

  8. Continuous anaerobic co-digestion of Ulva biomass and cheese whey at varying substrate mixing ratios: Different responses in two reactors with different operating regimes.

    PubMed

    Jung, Heejung; Kim, Jaai; Lee, Changsoo

    2016-12-01

    The feasibility of co-digestion of Ulva with whey was investigated at varying substrate mixing ratios in two continuous reactors run with increasing and decreasing proportions of Ulva, respectively. Co-digestion with whey proved beneficial to the biomethanation of Ulva, with the methane yield being greater by up to 1.6-fold in co-digestion phases than in the Ulva mono-digestion phases. The experimental reactors responded differently, in terms of process performance and community structure, to the changes in the substrate mixing ratio. This can be attributed to the different operating regimes between two reactors, which may have caused the microbial communities to develop in different ways to acclimate. Methanosaeta-related populations were the predominant methanogens responsible for the production of methane regardless of different substrate mixing ratios in both reactors. Considering the methane recovery and the Ulva treatment capacity, the optimal fraction of Ulva in the substrate mixture is suggested to be 50-75%.

  9. Mixing state, composition, and sources of fine aerosol particles in the Qinghai-Tibetan Plateau and the influence of agricultural biomass burning

    NASA Astrophysics Data System (ADS)

    Li, W. J.; Chen, S. R.; Xu, Y. S.; Guo, X. C.; Sun, Y. L.; Yang, X. Y.; Wang, Z. F.; Zhao, X. D.; Chen, J. M.; Wang, W. X.

    2015-09-01

    Transmission electron microscopy (TEM) was employed to obtain morphology, size, composition, and mixing state of background fine particles with diameter less than 1 μm in the Qinghai-Tibetan Plateau (QTP) during 15 September to 15 October 2013. Individual aerosol particles mainly contained secondary inorganic aerosols (SIA-sulfate and nitrate) and organics during clean periods (PM2.5: particles less than 2.5 μg m-3). The presence of KCl-NaCl associated with organics and an increase of soot particles suggest that an intense biomass burning event caused the highest PM2.5 concentrations (> 30 μg m-3) during the study. A large number fraction of the fly ash-containing particles (21.73 %) suggests that coal combustion emissions in the QTP significantly contributed to air pollutants at the median pollution level (PM2.5: 10-30 μg m-3). We concluded that emissions from biomass burning and from coal combustion both constantly contribute to anthropogenic particles in the QTP atmosphere. Based on size distributions of individual particles in different pollution levels, we found that gas condensation on existing particles is an important chemical process for the formation of SIA with organic coating. TEM observations show that refractory aerosols (e.g., soot, fly ash, and visible organic particles) likely adhere to the surface of SIA particles larger than 200 nm due to coagulation. Organic coating and soot on surface of the aged particles likely influence their hygroscopic and optical properties in the QTP, respectively. To our knowledge, this study reports the first microscopic analysis of fine particles in the background QTP air.

  10. Dynamic terahertz spectroscopy of gas molecules mixed with unwanted aerosol under atmospheric pressure using fibre-based asynchronous-optical-sampling terahertz time-domain spectroscopy.

    PubMed

    Hsieh, Yi-Da; Nakamura, Shota; Abdelsalam, Dahi Ghareab; Minamikawa, Takeo; Mizutani, Yasuhiro; Yamamoto, Hirotsugu; Iwata, Tetsuo; Hindle, Francis; Yasui, Takeshi

    2016-06-15

    Terahertz (THz) spectroscopy is a promising method for analysing polar gas molecules mixed with unwanted aerosols due to its ability to obtain spectral fingerprints of rotational transition and immunity to aerosol scattering. In this article, dynamic THz spectroscopy of acetonitrile (CH3CN) gas was performed in the presence of smoke under the atmospheric pressure using a fibre-based, asynchronous-optical-sampling THz time-domain spectrometer. To match THz spectral signatures of gas molecules at atmospheric pressure, the spectral resolution was optimized to 1 GHz with a measurement rate of 1 Hz. The spectral overlapping of closely packed absorption lines significantly boosted the detection limit to 200 ppm when considering all the spectral contributions of the numerous absorption lines from 0.2 THz to 1 THz. Temporal changes of the CH3CN gas concentration were monitored under the smoky condition at the atmospheric pressure during volatilization of CH3CN droplets and the following diffusion of the volatilized CH3CN gas without the influence of scattering or absorption by the smoke. This system will be a powerful tool for real-time monitoring of target gases in practical applications of gas analysis in the atmospheric pressure, such as combustion processes or fire accident.

  11. Dynamic terahertz spectroscopy of gas molecules mixed with unwanted aerosol under atmospheric pressure using fibre-based asynchronous-optical-sampling terahertz time-domain spectroscopy

    PubMed Central

    Hsieh, Yi-Da; Nakamura, Shota; Abdelsalam, Dahi Ghareab; Minamikawa, Takeo; Mizutani, Yasuhiro; Yamamoto, Hirotsugu; Iwata, Tetsuo; Hindle, Francis; Yasui, Takeshi

    2016-01-01

    Terahertz (THz) spectroscopy is a promising method for analysing polar gas molecules mixed with unwanted aerosols due to its ability to obtain spectral fingerprints of rotational transition and immunity to aerosol scattering. In this article, dynamic THz spectroscopy of acetonitrile (CH3CN) gas was performed in the presence of smoke under the atmospheric pressure using a fibre-based, asynchronous-optical-sampling THz time-domain spectrometer. To match THz spectral signatures of gas molecules at atmospheric pressure, the spectral resolution was optimized to 1 GHz with a measurement rate of 1 Hz. The spectral overlapping of closely packed absorption lines significantly boosted the detection limit to 200 ppm when considering all the spectral contributions of the numerous absorption lines from 0.2 THz to 1 THz. Temporal changes of the CH3CN gas concentration were monitored under the smoky condition at the atmospheric pressure during volatilization of CH3CN droplets and the following diffusion of the volatilized CH3CN gas without the influence of scattering or absorption by the smoke. This system will be a powerful tool for real-time monitoring of target gases in practical applications of gas analysis in the atmospheric pressure, such as combustion processes or fire accident. PMID:27301319

  12. Dynamic terahertz spectroscopy of gas molecules mixed with unwanted aerosol under atmospheric pressure using fibre-based asynchronous-optical-sampling terahertz time-domain spectroscopy

    NASA Astrophysics Data System (ADS)

    Hsieh, Yi-Da; Nakamura, Shota; Abdelsalam, Dahi Ghareab; Minamikawa, Takeo; Mizutani, Yasuhiro; Yamamoto, Hirotsugu; Iwata, Tetsuo; Hindle, Francis; Yasui, Takeshi

    2016-06-01

    Terahertz (THz) spectroscopy is a promising method for analysing polar gas molecules mixed with unwanted aerosols due to its ability to obtain spectral fingerprints of rotational transition and immunity to aerosol scattering. In this article, dynamic THz spectroscopy of acetonitrile (CH3CN) gas was performed in the presence of smoke under the atmospheric pressure using a fibre-based, asynchronous-optical-sampling THz time-domain spectrometer. To match THz spectral signatures of gas molecules at atmospheric pressure, the spectral resolution was optimized to 1 GHz with a measurement rate of 1 Hz. The spectral overlapping of closely packed absorption lines significantly boosted the detection limit to 200 ppm when considering all the spectral contributions of the numerous absorption lines from 0.2 THz to 1 THz. Temporal changes of the CH3CN gas concentration were monitored under the smoky condition at the atmospheric pressure during volatilization of CH3CN droplets and the following diffusion of the volatilized CH3CN gas without the influence of scattering or absorption by the smoke. This system will be a powerful tool for real-time monitoring of target gases in practical applications of gas analysis in the atmospheric pressure, such as combustion processes or fire accident.

  13. Cloud condensation nuclei (CCN) activity of aliphatic amine secondary aerosol

    NASA Astrophysics Data System (ADS)

    Tang, X.; Price, D.; Praske, E.; Vu, D. N.; Purvis-Roberts, K.; Silva, P. J.; Cocker, D. R., III; Asa-Awuku, A.

    2014-06-01

    Aliphatic amines can form secondary aerosol via oxidation with atmospheric radicals (e.g., hydroxyl radical and nitrate radical). The particle can contain both secondary organic aerosol (SOA) and inorganic salts. The ratio of organic to inorganic materials in the particulate phase influences aerosol hygroscopicity and cloud condensation nuclei (CCN) activity. SOA formed from trimethylamine (TMA) and butylamine (BA) reactions with hydroxyl radical (OH) is composed of organic material of low hygroscopicity (single hygroscopicity parameter, κ, ≤ 0.25). Secondary aerosol formed from the tertiary aliphatic amine (TMA) with N2O5 (source of nitrate radical, NO3) contains less volatile compounds than the primary aliphatic amine (BA) aerosol. As relative humidity (RH) increases, inorganic amine salts are formed as a result of acid-base reactions. The CCN activity of the humid TMA-N2O5 aerosol obeys Zdanovskii, Stokes, and Robinson (ZSR) ideal mixing rules. The humid BA + N2O5 aerosol products were found to be very sensitive to the temperature at which the measurements were made within the streamwise continuous-flow thermal gradient CCN counter; κ ranges from 0.4 to 0.7 dependent on the instrument supersaturation (ss) settings. The variance of the measured aerosol κ values indicates that simple ZSR rules cannot be applied to the CCN results from the primary aliphatic amine system. Overall, aliphatic amine aerosol systems' κ ranges within 0.2 < κ < 0.7. This work indicates that aerosols formed via nighttime reactions with amines are likely to produce hygroscopic and volatile aerosol, whereas photochemical reactions with OH produce secondary organic aerosol of lower CCN activity. The contributions of semivolatile secondary organic and inorganic material from aliphatic amines must be considered for accurate hygroscopicity and CCN predictions from aliphatic amine systems.

  14. Characterizing the Vertical Distribution of Aerosols Over the ARM SGP Site

    SciTech Connect

    Richard Ferrare, Connor Flynn, David Turner

    2009-05-05

    This project focused on: 1) evaluating the performance of the DOE ARM SGP Raman lidar system in measuring profiles of water vapor and aerosols, and 2) the use of the Raman lidar measurements of aerosol and water vapor profiles for assessing the vertical distribution of aerosols and water vapor simulated by global transport models and examining diurnal variability of aerosols and water vapor. The highest aerosol extinction was generally observed close to the surface during the nighttime just prior to sunrise. The high values of aerosol extinction are most likely associated with increased scattering by hygroscopic aerosols, since the corresponding average relative humidity values were above 70%. After sunrise, relative humidity and aerosol extinction below 500 m decreased with the growth in the daytime convective boundary layer. The largest aerosol extinction for altitudes above 1 km occurred during the early afternoon most likely as a result of the increase in relative humidity. The water vapor mixing ratio profiles generally showed smaller variations with altitude between day and night. We also compared simultaneous measurements of relative humidity, aerosol extinction, and aerosol optical thickness derived from the ARM SGP Raman lidar and in situ instruments on board a small aircraft flown routinely over the ARM SGP site. In contrast, the differences between the CARL and IAP aerosol extinction measurements are considerably larger. Aerosol extinction derived from the IAP measurements is, on average, about 30-40% less than values derived from the Raman lidar. The reasons for this difference are not clear, but may be related to the corrections for supermicron scattering and relative humidity that were applied to the IAP data. The investigators on this project helped to set up a major field mission (2003 Aerosol IOP) over the DOE ARM SGP site. One of the goals of the mission was to further evaluate the aerosol and water vapor retrievals from this lidar system

  15. High initial Sr isotopic ratios and evidence for magma mixing in the Pioneer batholith of southwest Montana

    SciTech Connect

    Arth, J.G.; Zen, E.; Sellers, G.; Hammarstrom, J.

    1986-05-01

    The northeast part of the composite Pioneer batholith of southwest Montana consists of Late Cretaceous calc-alkaline plutons that vary in composition as a function of age, changing from minor hornblende-biotite quartz diorite at about 76 m.y., to a small pluton of hornblende-biotite tonalite at about 74 m.y., to abundant biotite-hornblende granodiorite and biotite granite at about 72 m.y., to some biotite granodiorite and 2-mica granite at 67 to 65 m.y. Initial /sup 87/Sr//sup 86/Sr ratios (SIRs) for the plutons range from 0.7112 to 0.7160. Magmas having a SIR near 0.7112 appear in most episodes of emplacement, whereas those having higher values are restricted to individual episodes. Two granodiorite plutons of 72 m.y. age show a mutual gradational contact, across which the SIR varies over a distance of 7 km from 0.711 to 0.714. The variation is ascribed to mixing between contemporaneous but isotopically distinct granodiorite magmas. The high SIRs of the batholith are interpreted as reflecting partial melting of portions of Precambrian lower crustal lithosphere to produce mafic to intermediate magma. The source may be similar to parts of Proterozoic gneisses now exposed at the surface. Mafic to intermediate magma may have fractionally crystallized at depth and released residual magma episodically to the upper crust over approximately 11 m.y. The high SIR of the Pioneer batholith is broadly similar to that of large parts of the Idaho batholith to the west, but is distinct from the SIR of the Boulder batholith to the northeast. A significant crustal discontinuity may separate the Pioneer-Idaho region from the Boulder region.

  16. Nighttime lidar water vapor mixing ratio profiling over Warsaw - impact of the relative humidity profile on cloud formation

    NASA Astrophysics Data System (ADS)

    Costa Surós, Montserrat; Stachlewska, Iwona S.

    2016-04-01

    A long-term study, assessing ground-based remote Raman lidar versus in-situ radiosounding has been conducted with the aim of improving the knowledge on the water content vertical profile through the atmosphere, and thus the conditions for cloud formation processes. Water vapor mixing ratio (WVMR) and relative humidity (RH) profiles were retrieved from ADR Lidar (PollyXT-type, EARLINET site in Warsaw). So far, more than 100 nighttime profiles averaged over 1h around midnight from July 2013 to December 2015 have been investigated. Data were evaluated with molecular extinctions calculated using two approximations: the US62 standard atmosphere and the radiosounding launched in Legionowo (12374). The calibration factor CH2O for lidar retrievals was obtained for each profile using the regression method and the profile method to determine the best calibration factor approximation to be used in the final WVMR and RH calculation. Thus, statistically representative results for comparisons between lidar WVMR median profiles obtained by calibrating using radiosounding profiles and using atmospheric synthetic profiles, all of them with the best calibration factor, will be presented. Finally, in order to constrain the conditions of cloud formation in function of the RH profile, the COS14 algorithm, capable of deriving cloud bases and tops by applying thresholds to the RH profiles, was applied to find the cloud vertical structure (CVS). The algorithm was former applied to radiosounding profiles at SGP-ARM site and tested against the CVS obtained from the Active Remote Sensing of Clouds (ARSCL) data. Similarly, it was applied for lidar measurements at the Warsaw measurement site.

  17. Multilevel Nonlinear Mixed-Effect Crown Ratio Models for Individual Trees of Mongolian Oak (Quercus mongolica) in Northeast China.

    PubMed

    Fu, Liyong; Zhang, Huiru; Lu, Jun; Zang, Hao; Lou, Minghua; Wang, Guangxing

    2015-01-01

    In this study, an individual tree crown ratio (CR) model was developed with a data set from a total of 3134 Mongolian oak (Quercus mongolica) trees within 112 sample plots allocated in Wangqing Forest Bureau of northeast China. Because of high correlation among the observations taken from the same sampling plots, the random effects at levels of both blocks defined as stands that have different site conditions and plots were taken into account to develop a nested two-level nonlinear mixed-effect model. Various stand and tree characteristics were assessed to explore their contributions to improvement of model prediction. Diameter at breast height, plot dominant tree height and plot dominant tree diameter were found to be significant predictors. Exponential model with plot dominant tree height as a predictor had a stronger ability to account for the heteroskedasticity. When random effects were modeled at block level alone, the correlations among the residuals remained significant. These correlations were successfully reduced when random effects were modeled at both block and plot levels. The random effects from the interaction of blocks and sample plots on tree CR were substantially large. The model that took into account both the block effect and the interaction of blocks and sample plots had higher prediction accuracy than the one with the block effect and population average considered alone. Introducing stand density into the model through dummy variables could further improve its prediction. This implied that the developed method for developing tree CR models of Mongolian oak is promising and can be applied to similar studies for other tree species.

  18. Acid rock drainage passive remediation: Potential use of alkaline clay, optimal mixing ratio and long-term impacts.

    PubMed

    Plaza, Fernando; Wen, Yipei; Perone, Hanna; Xu, Yi; Liang, Xu

    2017-01-15

    Acid rock drainage (ARD) is one of the most adverse environmental problems of the mining industry. Surface and ground water affected by this pollution are characterized by their acidity and the high content of sulfates and metals/metalloids. In this study, alkaline clay (AC), an industrial waste with a high alkalinity, which is utilized in the alumina refining process, was used as the remediation material to inhibit pyrite oxidation in waste coal piles. Through a series of laboratory experiments (static and kinetic), complemented with field measurements and geochemical modeling, three important issues associated with this passive and sustainable ARD remediation method were investigated: 1) the potential use of alkaline clay as an ARD remediation material, 2) the adequate alkaline clay/coal refuse mixing ratio (AC/CR) to ensure pH values close to neutral conditions, and, 3) the implications for long-term performance, in terms of the trends of the main parameters involved in this process such as pH, concentrations of sulfate, iron and other dissolved contaminants. Both field measurements and the samples used for the experiments came from a local waste coal site. Through the analysis of the field measurements and the outcome of the laboratory experiments, AC proved to be an effective remediation material for ARD. Compared to those found in mine tailings, the concentrations of contaminants such as iron, manganese or sulfate were significantly reduced with this remediation approach. Moreover, results suggest a reliable long-term stability of the remediation (i.e. neutral pH conditions are maintained), thus enhancing the generation of iron precipitates that could produce pyrite grain coating. These processes also made the amended layer less porous, thus increased water retention and hindered oxygen diffusion.

  19. Multilevel Nonlinear Mixed-Effect Crown Ratio Models for Individual Trees of Mongolian Oak (Quercus mongolica) in Northeast China

    PubMed Central

    Fu, Liyong; Zhang, Huiru; Lu, Jun; Zang, Hao; Lou, Minghua; Wang, Guangxing

    2015-01-01

    In this study, an individual tree crown ratio (CR) model was developed with a data set from a total of 3134 Mongolian oak (Quercus mongolica) trees within 112 sample plots allocated in Wangqing Forest Bureau of northeast China. Because of high correlation among the observations taken from the same sampling plots, the random effects at levels of both blocks defined as stands that have different site conditions and plots were taken into account to develop a nested two-level nonlinear mixed-effect model. Various stand and tree characteristics were assessed to explore their contributions to improvement of model prediction. Diameter at breast height, plot dominant tree height and plot dominant tree diameter were found to be significant predictors. Exponential model with plot dominant tree height as a predictor had a stronger ability to account for the heteroskedasticity. When random effects were modeled at block level alone, the correlations among the residuals remained significant. These correlations were successfully reduced when random effects were modeled at both block and plot levels. The random effects from the interaction of blocks and sample plots on tree CR were substantially large. The model that took into account both the block effect and the interaction of blocks and sample plots had higher prediction accuracy than the one with the block effect and population average considered alone. Introducing stand density into the model through dummy variables could further improve its prediction. This implied that the developed method for developing tree CR models of Mongolian oak is promising and can be applied to similar studies for other tree species. PMID:26241912

  20. Airborne Remote-Sensing of Atmoshperic CH4 and CO2 Column Mixing Ratio With MAMap - First Results

    NASA Astrophysics Data System (ADS)

    Tretner, A.; Gerilowski, K.; Bovensmann, H.; Buchwitz, M.; Erzinger, J.; Burrows, J.

    2007-12-01

    The Methane Airborne Mapper (MAMap) performs quantitative CO2 and CH4 remote sensing measurements of the atmospheric column between an aircraft and the Earth's surface. Its two spectrometers cover wavelenghts of 1.59-1.62μm for CO2, 1.63-1.75μm for CH4 and 760nm for O2. A CH4 detection limit of <35ppbv and a resolution of <5% (at atmospheric background concentration of 1750ppbv) have been ascertained, which makes it possible to detect small changes within the atmospheric CH4 column at a local and regional scale. The atmospheric column mixing ratios of CH4 and CO2 were calculated using the WFM-DOAS algorithm which is known from the retrieval of CH4 and CO2 column concentrations from nadir measurements by SCIAMACHY. MAMap addresses the uncertainties in the current greenhouse gas emission budgets and provides a link between local ground-based small-scale and global satellite-based measurements. The aim of future MAMap research programs is the detection and quantification of CH4 and CO2 emission sources of both natural and anthropogenic origin. MAMap is designed for flexible operations at various planes, e.g. the DLR Dornier 228, the DLR 'Falcon' or the DLR Gulfstream 'HALO' aircraft. The results presented here were performed with a Cessna aircraft T207 at a flight height of 700m and a flight speed of 200km/h. The related ground pixel size covers 18m (across-track) x 10m (along track, albedo 0.18). The preliminary assessment of the sensor sensitivity under field campaign conditions includes measurements over a variety of natural and anthropogenic CH4 and CO2 emission sources, like coal-fired power plants, landfill sites, wetlands, a large number of different land surface types and a simulated CH4 source (CH4 released from a pressured gas bottle). First results will be reported.

  1. Aerosol backscatter studies supporting LAWS

    NASA Technical Reports Server (NTRS)

    Rothermel, Jeffry

    1989-01-01

    Optimized Royal Signals and Radar Establishment (RSRE), Laser True Airspeed System (LATAS) algorithm for low backscatter conditions was developed. The algorithm converts backscatter intensity measurements from focused continuous-wave (CW) airborne Doppler lidar into backscatter coefficients. The performance of optimized algorithm under marginal backscatter signal conditions was evaluated. The 10.6 micron CO2 aerosol backscatter climatologies were statistically analyzed. Climatologies reveal clean background aerosol mode near 10(exp -10)/kg/sq m/sr (mixing ratio units) through middle and upper troposhere, convective mode associated with planetary boundary layer convective activity, and stratospheric mode associated with volcanically-generated aerosols. Properties of clean background mode are critical to design and simulation studies of Laser Atmospheric Wind Sounder (LAWS), a MSFC facility Instrument on the Earth Observing System (Eos). Previous intercomparisons suggested correlation between aerosol backscatter at CO2 wavelength and water vapor. Field measurements of backscatter profiles with MSFC ground-based Doppler lidar system (GBDLS) were initiated in late FY-88 to coincide with independent program of local rawinsonde releases and overflights by Multi-spectral Atmospheric Mapping Sensor (MAMS), a multi-channel infrared radiometer capable of measuring horizontal and vertical moisture distributions. Design and performance simulation studies for LAWS would benefit from the existence of a relationship between backscatter and water vapor.

  2. Using Raman-lidar-based regularized microphysical retrievals and Aerosol Mass Spectrometer measurements for the characterization of biomass burning aerosols

    NASA Astrophysics Data System (ADS)

    Samaras, Stefanos; Nicolae, Doina; Böckmann, Christine; Vasilescu, Jeni; Binietoglou, Ioannis; Labzovskii, Lev; Toanca, Florica; Papayannis, Alexandros

    2015-10-01

    In this work we extract the microphysical properties of aerosols for a collection of measurement cases with low volume depolarization ratio originating from fire sources captured by the Raman lidar located at the National Institute of Optoelectronics (INOE) in Bucharest. Our algorithm was tested not only for pure smoke but also for mixed smoke and urban aerosols of variable age and growth. Applying a sensitivity analysis on initial parameter settings of our retrieval code was proved vital for producing semi-automatized retrievals with a hybrid regularization method developed at the Institute of Mathematics of Potsdam University. A direct quantitative comparison of the retrieved microphysical properties with measurements from a Compact Time of Flight Aerosol Mass Spectrometer (CToF-AMS) is used to validate our algorithm. Microphysical retrievals performed with sun photometer data are also used to explore our results. Focusing on the fine mode we observed remarkable similarities between the retrieved size distribution and the one measured by the AMS. More complicated atmospheric structures and the factor of absorption appear to depend more on particle radius being subject to variation. A good correlation was found between the aerosol effective radius and particle age, using the ratio of lidar ratios (LR: aerosol extinction to backscatter ratios) as an indicator for the latter. Finally, the dependence on relative humidity of aerosol effective radii measured on the ground and within the layers aloft show similar patterns.

  3. MEASUREMENT AND INTERPRETATION OF ISOPRENE FLUXES AND ISOPRENE, METHACROLEIN, AND METHYL VINYL KETONE MIXING RATIOS AT THE PROPHET SITE DURING THE 1998 INTENSIVE

    EPA Science Inventory

    Mixing ratios of isoprene, methyl vinyl ketone (MVK), and methacrolein (MACR) were determined continuously during an 8-day period in the summer of 1998 at a rural forested site located within the University of Michigan Biological Station (UMBS). The measurements were obtained as ...

  4. Black carbon in aerosol during BIBLE B

    NASA Astrophysics Data System (ADS)

    Liley, J. Ben; Baumgardner, D.; Kondo, Y.; Kita, K.; Blake, D. R.; Koike, M.; Machida, T.; Takegawa, N.; Kawakami, S.; Shirai, T.; Ogawa, T.

    2003-02-01

    The Biomass Burning and Lightning Experiment (BIBLE) A and B campaigns over the tropical western Pacific during springtime deployed a Gulfstream-II aircraft with systems to measure ozone and numerous precursor species. Aerosol measuring systems included a MASP optical particle counter, a condensation nucleus (CN) counter, and an absorption spectrometer for black carbon. Aerosol volume was very low in the middle and upper troposphere during both campaigns, and during BIBLE A, there was little aerosol enhancement in the boundary layer away from urban areas. In BIBLE B, there was marked aerosol enhancement in the lowest 3 km of the atmosphere. Mixing ratios of CN in cloud-free conditions in the upper troposphere were in general higher than in the boundary layer, indicating new particle formation from gaseous precursors. High concentrations of black carbon were observed during BIBLE B, with mass loadings up to 40 μg m-3 representing as much as one quarter of total aerosol mass. Strong correlations with hydrocarbon enhancement allow the determination of a black carbon emission ratio for the fires at that time. Expressed as elemental carbon, it is about 0.5% of carbon dioxide and 6% of carbon monoxide emissions from the same fires, comparable to methane production, and greater than that of other hydrocarbons.

  5. Black carbon in aerosol during BIBLE B

    NASA Astrophysics Data System (ADS)

    Liley, J. Ben; Baumgardner, D.; Kondo, Y.; Kita, K.; Blake, D. R.; Koike, M.; Machida, T.; Takegawa, N.; Kawakami, S.; Shirai, T.; Ogawa, T.

    2002-02-01

    The Biomass Burning and Lightning Experiment (BIBLE) A and B campaigns over the tropical western Pacific during springtime deployed a Gulfstream-II aircraft with systems to measure ozone and numerous precursor species. Aerosol measuring systems included a MASP optical particle counter, a condensation nucleus (CN) counter, and an absorption spectrometer for black carbon. Aerosol volume was very low in the middle and upper troposphere during both campaigns, and during BIBLE A, there was little aerosol enhancement in the boundary layer away from urban areas. In BIBLE B, there was marked aerosol enhancement in the lowest 3 km of the atmosphere. Mixing ratios of CN in cloud-free conditions in the upper troposphere were in general higher than in the boundary layer, indicating new particle formation from gaseous precursors. High concentrations of black carbon were observed during BIBLE B, with mass loadings up to 40 μg m-3 representing as much as one quarter of total aerosol mass. Strong correlations with hydrocarbon enhancement allow the determination of a black carbon emission ratio for the fires at that time. Expressed as elemental carbon, it is about 0.5% of carbon dioxide and 6% of carbon monoxide emissions from the same fires, comparable to methane production, and greater than that of other hydrocarbons.

  6. Airborne LIDAR Measurements of Aerosol and Ozone Above the Alberta Oil Sands Region

    NASA Astrophysics Data System (ADS)

    Aggarwal, M.; Whiteway, J. A.; Seabrook, J.; Gray, L. H.

    2014-12-01

    Lidar measurements of ozone and aerosol were conducted from a Twin Otter aircraft above the oil sands region of northern Alberta. The field campaign was carried out with a total of five flights out of Fort McMurray, Alberta during the period between August 22 and August 26, 2013. Significant amounts of aerosol were observed within the boundary layer, up to a height of 1.6 km, but the ozone concentration remained at or below background levels. On August 24th the lidar observed a separated layer of aerosol above the boundary layer, at a height of 1.8 km, in which the ozone mixing ratio increased to 70 ppbv. Backward trajectory calculations revealed that the air containing this separated aerosol layer had passed over an area of forest fires. Directly below the layer of forest fire smoke, in the pollution from the oil sands industry, the measured ozone mixing ratio was lower than the background levels (≤35 ppbv).

  7. Large mixing ratios of atmospheric nitrous acid (HONO) at Concordia (East Antarctic Plateau) in summer: a strong source from surface snow?

    NASA Astrophysics Data System (ADS)

    Legrand, M.; Preunkert, S.; Frey, M.; Bartels-Rausch, Th.; Kukui, A.; King, M. D.; Savarino, J.; Kerbrat, M.; Jourdain, B.

    2014-09-01

    During the austral summer 2011/2012 atmospheric nitrous acid (HONO) was investigated for the second time at the Concordia site (75°06' S, 123°33' E), located on the East Antarctic Plateau, by deploying a long-path absorption photometer (LOPAP). Hourly mixing ratios of HONO measured in December 2011/January 2012 (35 ± 5.0 pptv) were similar to those measured in December 2010/January 2011 (30.4 ± 3.5 pptv). The large value of the HONO mixing ratio at the remote Concordia site suggests a local source of HONO in addition to weak production from oxidation of NO by the OH radical. Laboratory experiments demonstrate that surface snow removed from Concordia can produce gas-phase HONO at mixing ratios half that of the NOx mixing ratio produced in the same experiment at typical temperatures encountered at Concordia in summer. Using these lab data and the emission flux of NOx from snow estimated from the vertical gradient of atmospheric concentrations measured during the campaign, a mean diurnal HONO snow emission ranging between 0.5 and 0.8 × 109 molecules cm-2 s-1 is calculated. Model calculations indicate that, in addition to around 1.2 pptv of HONO produced by the NO oxidation, these HONO snow emissions can only explain 6.5 to 10.5 pptv of HONO in the atmosphere at Concordia. To explain the difference between observed and simulated HONO mixing ratios, tests were done both in the field and at lab to explore the possibility that the presence of HNO4 had biased the measurements of HONO.

  8. Observations of molecular hydrogen mixing ratio and stable isotopic composition at the Cabauw tall tower in the Netherlands

    NASA Astrophysics Data System (ADS)

    Batenburg, A. M.; Popa, M. E.; Vermeulen, A. T.; van den Bulk, W. C. M.; Jongejan, P. A. C.; Fisher, R. E.; Lowry, D.; Nisbet, E. G.; Röckmann, T.

    2016-12-01

    Measurements of the stable isotopic composition (δD(H2) or δD) of atmospheric molecular hydrogen (H2) are a useful addition to mixing ratio (χ(H2)) measurements for understanding the atmospheric H2 cycle. δD datasets published so far consist mostly of observations at background locations. We complement these with observations from the Cabauw tall tower at the CESAR site, situated in a densely populated region of the Netherlands. Our measurements show a large anthropogenic influence on the local H2 cycle, with frequently occurring pollution events that are characterized by χ(H2) values that reach up to ≈1 ppm and low δD values. An isotopic source signature analysis yields an apparent source signature below -400‰, which is much more D-depleted than the fossil fuel combustion source signature commonly used in H2 budget studies. Two diurnal cycles that were sampled at a suburban site near London also show a more D-depleted source signature (≈-340‰), though not as extremely depleted as at Cabauw. The source signature of the Northwest European vehicle fleet may have shifted to somewhat lower values due to changes in vehicle technology and driving conditions. Even so, the surprisingly depleted apparent source signature at Cabauw requires additional explanation; microbial H2 production seems the most likely cause. The Cabauw tower site also allowed us to sample vertical profiles. We found no decrease in χ(H2) at lower sampling levels (20 and 60 m) with respect to higher sampling levels (120 and 200 m). There was a significant shift to lower median δD values at the lower levels. This confirms the limited role of soil uptake around Cabauw, and again points to microbial H2 production during an extended growing season, as well as to possible differences in average fossil fuel combustion source signature between the different footprint areas of the sampling levels. So, although knowledge of the background cycle of H2 has improved over the last decade, surprising

  9. Temporal Variation of Aerosol Properties at a Rural Continental Site and Study of Aerosol Evolution through Growth Law Analysis

    NASA Technical Reports Server (NTRS)

    Wang, Jian; Collins, Don; Covert, David; Elleman, Robert; Ferrare, Richard A.; Gasparini, Roberto; Jonsson, Haflidi; Ogren, John; Sheridan, Patrick; Tsay, Si-Chee

    2006-01-01

    Aerosol size distributions were measured by a Scanning Mobility Particle Sizer (SMPS) onboard the CIRPAS Twin Otter aircraft during 16 flights at the Southern Great Plains (SGP) site in northern central Oklahoma as part of the Aerosol Intensive Operation period in May, 2003. During the same period a second SMPS was deployed at a surface station and provided continuous measurements. Combined with trace gas measurements at the SGP site and back-trajectory analysis, the aerosol size distributions provided insights into the sources of aerosols observed at the SGP site. High particle concentrations, observed mostly during daytime, were well correlated with the sulfur dioxide (SO2) mixing ratios, suggesting nucleation involving sulfuric acid is likely the main source of newly formed particles at the SGP. Aerosols within plumes originating from wildfires in Central America were measured at the surface site. Vertically compact aerosol layers, which can be traced back to forest fires in East Asia, were intercepted at altitudes over 3000 meters. Analyses of size dependent particle growth rates for four periods during which high cloud coverage was observed indicate growth dominated by volume controlled reactions. Sulfate accounts for 50% to 72% of the increase in aerosol volume concentration; the rest of the volume concentration increase was likely due to secondary organic species. The growth law analyses and meteorological conditions indicate that the sulfate was produced mainly through aqueous oxidation of SO2 in clouds droplets and hydrated aerosol particles.

  10. Stable Carbon Isotope Ratios and Mixing Ratios of Several VOC Including n-Hexane, Benzene, Toluene, p-Xylene, n-Octane, and n-Decane Measured During the Border Air Quality Study Campaign (June-July, 2007)

    NASA Astrophysics Data System (ADS)

    Kornilova, A.; Moukhtar, S.; Huang, L.; Rudolph, J.

    2008-12-01

    Many important secondary pollutants are formed during the oxidation of Volatile Organic Compounds (VOC) in the atmosphere. These organic compounds can contribute significant mass to atmospheric particulate matter (PM) and therefore impact physical properties and composition of aerosols. Despite numerous studies, the formation processes for atmospheric PM are still not well understood. While there have been very extensive laboratory investigations of PM formation, nearly all of these studies have been conducted at VOC concentrations which exceed ambient atmospheric levels by several orders of magnitude. Consequently there is substantial uncertainty in the extrapolation of laboratory results to the atmosphere. Recently it has been demonstrated that stable carbon isotopic composition measurements can be very valuable in providing increased insight into the chemical and transport processes of VOC in the troposphere. Studies showed that isotope ratio measurements could aid in the determination of photochemical processing of individual VOC. It is expected that applying isotope measurements to studies of VOC oxidation products in the atmosphere will allow to establish quantitative relationship between the amount of precursor oxidized and the concentration of secondary pollutants formed during this process. Thus, the yield of secondary organic aerosols (SOA) from this reaction can be calculated. A cartridge technique was developed for field sampling of VOC and subsequent laboratory analysis by gas chromatography coupled with isotope ratio mass spectrometry. It was first implemented during the BAQS field study (June-July, 2007) parallel to PM sampling. Stable carbon isotopic composition and concentrations of several VOC were determined and compared to those of PM. The results of these measurements will be presented and discussed.

  11. Final Technical Report for "Ice nuclei relation to aerosol properties: Data analysis and model parameterization for IN in mixed-phase clouds" (DOE/SC00002354)

    SciTech Connect

    Anthony Prenni; Kreidenweis, Sonia M.

    2012-09-28

    Clouds play an important role in weather and climate. In addition to their key role in the hydrologic cycle, clouds scatter incoming solar radiation and trap infrared radiation from the surface and lower atmosphere. Despite their importance, feedbacks involving clouds remain as one of the largest sources of uncertainty in climate models. To better simulate cloud processes requires better characterization of cloud microphysical processes, which can affect the spatial extent, optical depth and lifetime of clouds. To this end, we developed a new parameterization to be used in numerical models that describes the variation of ice nuclei (IN) number concentrations active to form ice crystals in mixed-phase (water droplets and ice crystals co-existing) cloud conditions as these depend on existing aerosol properties and temperature. The parameterization is based on data collected using the Colorado State University continuous flow diffusion chamber in aircraft and ground-based campaigns over a 14-year period, including data from the DOE-supported Mixed-Phase Arctic Cloud Experiment. The resulting relationship is shown to more accurately represent the variability of ice nuclei distributions in the atmosphere compared to currently used parameterizations based on temperature alone. When implemented in one global climate model, the new parameterization predicted more realistic annually averaged cloud water and ice distributions, and cloud radiative properties, especially for sensitive higher latitude mixed-phase cloud regions. As a test of the new global IN scheme, it was compared to independent data collected during the 2008 DOE-sponsored Indirect and Semi-Direct Aerosol Campaign (ISDAC). Good agreement with this new data set suggests the broad applicability of the new scheme for describing general (non-chemically specific) aerosol influences on IN number concentrations feeding mixed-phase Arctic stratus clouds. Finally, the parameterization was implemented into a regional

  12. Absorbing aerosols at high relative humidity: linking hygroscopic growth to optical properties

    NASA Astrophysics Data System (ADS)

    Flores, J. Michel; Bar-Or, R. Z.; Bluvshtein, N.; Abo-Riziq, A.; Kostinski, A.; Borrmann, S.; Koren, I.; Koren, I.; Rudich, Y.

    2012-06-01

    One of the major uncertainties in the understanding of Earth's climate system is the interaction between solar radiation and aerosols in the atmosphere. Aerosols exposed to high humidity will change their chemical, physical, and optical properties due to their increased water content. To model hydrated aerosols, atmospheric chemistry and climate models often use the volume weighted mixing rule to predict the complex refractive index (RI) of aerosols when they interact with high relative humidity, and, in general, assume homogeneous mixing. This study explores the validity of these assumptions. A humidified cavity ring down aerosol spectrometer (CRD-AS) and a tandem hygroscopic DMA (differential mobility analyzer) are used to measure the extinction coefficient and hygroscopic growth factors of humidified aerosols, respectively. The measurements are performed at 80% and 90%RH at wavelengths of 532 nm and 355 nm using size-selected aerosols with different degrees of absorption; from purely scattering to highly absorbing particles. The ratio of the humidified to the dry extinction coefficients (fRHext(%RH, Dry)) is measured and compared to theoretical calculations based on Mie theory. Using the measured hygroscopic growth factors and assuming homogeneous mixing, the expected RIs using the volume weighted mixing rule are compared to the RIs derived from the extinction measurements. We found a weak linear dependence or no dependence of fRH(%RH, Dry) with size for hydrated absorbing aerosols in contrast to the non-monotonically decreasing behavior with size for purely scattering aerosols. No discernible difference could be made between the two wavelengths used. Less than 7% differences were found between the real parts of the complex refractive indices derived and those calculated using the volume weighted mixing rule, and the imaginary parts had up to a 20% difference. However, for substances with growth factor less than 1.15 the volume weighted mixing rule assumption

  13. Raman Lidar Profiling of Aerosols Over the Central US; Diurnal Variability and Comparisons with the GOCART Model

    NASA Technical Reports Server (NTRS)

    Ferrare, R. A.; Chin, M.; Clayton, M.; Turner, D.

    2002-01-01

    We use profiles of aerosol extinction, water vapor mixing ratio, and relative humidity measured by the ARM SGP Raman lidar in northern Oklahoma to show how the vertical distributions of aerosol extinction and water vapor vary throughout the diurnal cycle. While significant (20-30%) variations in aerosol extinction occurred near the surface as well as aloft, smaller (approximately 10%) variations were observed in the diurnal variability of aerosol optical thickness (AOT). The diurnal variations in aerosol extinction profiles are well correlated with corresponding variations in the average relative humidity profiles. The water vapor mixing ratio profiles and integrated water vapor amounts generally show less diurnal variability. The Raman lidar profiles are also used to evaluate the aerosol optical thickness and aerosol extinction profiles simulated by the GOCART global aerosol model. Initial comparisons show that the AOT simulated by GOCART was in closer agreement with the AOT derived from the Raman lidar and Sun photometer measurements during November 2000 than during September 2000. For both months, the vertical variability in average aerosol extinction profiles simulated by GOCART is less than the variability in the corresponding Raman lidar profiles.

  14. Fast-response CO2 mixing-ratio measurement with an open-path gas analyzer for eddy-flux applications

    NASA Astrophysics Data System (ADS)

    Bogoev, I.

    2014-12-01

    Infra-red gas analyzers operate on the principle of light absorption and measure the density of the gas in the sensing path. To account for density fluctuations caused by barometric pressure, thermal expansion and contraction, and water-vapor dilution, flux calculations using CO2 density measurements need to be corrected for sensible and latent heat transfer (also known as WPL corrections). In contrast, these corrections are not required if the flux calculation involves CO2 mixing ratio relative to dry air. Historically, CO2 mixing ratio measurements have been available only for analyzers with a closed-path where temperature fluctuations in the air sample are attenuated in the intake tubing to a level that they are adequately measured by a contact thermometer. Open-path gas analyzers are not able to make in situ CO2 mixing-ratio measurements because of the unavailability of a reliable, accurate and fast-response air-temperature sensor in the optical path. A newly developed eddy-flux system integrates an aerodynamic open-path gas analyzer with a sonic anemometer where the sensing volumes of the two instruments coincide. Thus the system has the ability to provide temporally and spatially synchronized fast-response measurements of the 3D wind vector, sonically derived air temperature, CO2 and water vapor densities. When these measurements are combined with a fast-response static pressure measurement an instantaneous in-situ CO2 mixing ratio can be calculated on-line, eliminating the need for density corrections in post-processing. In this study fluxes computed from CO2 mixing-ratio are compared to WPL corrected fluxes using CO2 density. Results from a field inter-comparison with an aspirated temperature probe suggest that accurate, fast response air temperature can be derived from humidity-corrected speed of sound measurements. Biases due to heat exchange with the analyzer surface are evaluated by comparing atmospheric sensible heat flux measurements with a

  15. Vertical structure of aerosols, temperature, and moisture associated with an intense African dust event observed over the eastern Caribbean

    NASA Astrophysics Data System (ADS)

    Jung, Eunsil; Albrecht, Bruce; Prospero, Joseph M.; Jonsson, Haflidi H.; Kreidenweis, Sonia M.

    2013-05-01

    unusually intense African dust event affected a large area of the western Atlantic and eastern Caribbean in early April 2010. Measurements made east of Barbados from the Center for Interdisciplinary Remotely Piloted Aircraft Studies (CIRPAS) Twin Otter research aircraft are used to characterize particle size distributions; vertical distributions of aerosols, temperature, and moisture; and processes leading to the observed stratification in the boundary layer. The vertical profiles of various aerosol characterizations were similar on both days and show three layers with distinct aerosol and thermodynamic characteristics: the Saharan Air Layer (SAL; ~2.2 km ± 500 m), a subcloud layer (SCL; surface to ~500 m), and an intermediate layer extending between them. The SAL and SCL display well-mixed aerosol and thermodynamic characteristics; but the most significant horizontal and vertical variations in aerosols and thermodynamics occur in the intermediate layer. The aerosol variability observed in the intermediate layer is likely associated with modification by shallow cumulus convection occurring sometime in the prior history of the air mass as it is advected across the Atlantic. A comparison of the thermodynamic structure observed in the event from its origin over Africa with that when it reached Barbados indicates that the lower part of the SAL was moistened by surface fluxes as the air mass was advected across the Atlantic. Mixing diagrams using aerosol concentrations and water vapor mixing ratios as conserved parameters provide insight into the vertical transports and mixing processes that may explain the observed aerosol and thermodynamic variability in each layer.

  16. Using the Mixed Effect Model as an Alternative Approach to Improve Correlation between Satellite Derived Aerosol Optical Depth (MISR & MODIS) and Ground Measured PM2.5 Data

    NASA Astrophysics Data System (ADS)

    Cabanes, H. V. O.; Lagrosas, N.

    2014-12-01

    The study seeks to determine the efficacy of using aerosol optical depth (AOD) data from MISR and MODIS as a surrogate for ground-based particulate matter (PM2.5) data by using AOD as an input for various computational methods. The data set used in the study ranged from January 2011 to December 2012. The advantage of the mixed effects model is in its ability to consider temporally changing attributes through the inclusion of random effects in the regression model. The study first established that MISR and MODIS AOD has a correlation with ground measured PM2.5 through regression analysis thereby providing rationale for further analysis. The regression analyses resulted in an R2 of 0.7513 and 0.7536 for MODIS and MISR, respectively. With the rationale established, data quality improvement measures were carried out through data screening and empirical correction. The data screening process involved the removal of data entries in which the absolute difference of MODIS and MISR AOD values deviated far more than the average of the data set. On the other hand, empirical correction was done by developing correction equations through multivariate regression with ground parameters such as AERONET AOD, relative humidity, and wind speed. Both methods were found to yield marked improvement in the correlation of satellite-derived AOD with PM2.5. After data quality had been improved, several computational methods are assessed by solving for the R2 and absolute error percentage. The methods are simple linear regression with MODIS (R2 = 0.7764, 18.43%) and MISR (R2 = 0.7614, 17.99%), multivariate linear regression with MODIS and MISR together (R2 = 0.8721, 13.63%), artificial neural network with MODIS and MISR as inputs (R2 = 0.8764, 13.45%), and the mixed effects model with MODIS and MISR as predictors (R2 = 0.9793, 5.20%). Among these, the mixed effects model performed the best and further error analysis showing an error that was independent on seasonality and dependent on the PM

  17. Mixing of anthropogenic dust and carbonaceous aerosols in seasonal snow on snow albedo reduction in 2014 China survey

    NASA Astrophysics Data System (ADS)

    Wang, Xin; Huang, Jianping; Pu, Wei

    2016-04-01

    Anthropogenic dusts produced from the affected by human activities derived from the industrial areas and carbonaceous aerosols (black carbon and organic carbon) deposited into snow or ice core via wet and dry deposition play key roles to the regional and global climate. Recently, a China survey was performed to measure the concentrations of insoluble light-absorbing particles (ILAP) in seasonal snow across northern China in January and February of 2014. The results indicate that the higher concentration of NO3- and SO42- and heavy metals of Zn, Pb, Cd, Ni, and Cu are likely to be attributed to enhanced local industrial emissions due to human activities. The emissions from fossil fuel combustion and biomass burning are likely to be important for the chemical elements in the seasonal snow with long-range transport, while medium enrichment factors of Mg, Ca, and Al were predominantly associated with soil dust, which is the most important natural source. There are large ranges of the BC and AD in seasonal snow over northeast China because of the anthropogenic emissions, which are caused by human activities. In addition, although the values of the snow albedo by model simulations are little higher in the visible to near-infrared wavelength than that during the China survey, the surface snow albedo by field campaign measurements have good agreement with the model simulations in the visible wavelength.

  18. Automated Chemical Analysis of Internally Mixed Aerosol Particles Using X-ray Spectromicroscopy at the Carbon K-Edge

    SciTech Connect

    Gilles, Mary K; Moffet, R.C.; Henn, T.; Laskin, A.

    2011-01-20

    We have developed an automated data analysis method for atmospheric particles using scanning transmission X-ray microscopy coupled with near edge X-ray fine structure spectroscopy (STXM/NEXAFS). This method is applied to complex internally mixed submicrometer particles containing organic and inorganic material. Several algorithms were developed to exploit NEXAFS spectral features in the energy range from 278 to 320 eV for quantitative mapping of the spatial distribution of elemental carbon, organic carbon, potassium, and noncarbonaceous elements in particles of mixed composition. This energy range encompasses the carbon K-edge and potassium L2 and L3 edges. STXM/NEXAFS maps of different chemical components were complemented with a subsequent analysis using elemental maps obtained by scanning electron microscopy coupled with energy dispersive X-ray analysis (SEM/EDX). We demonstrate the application of the automated mapping algorithms for data analysis and the statistical classification of particles.

  19. Aerosol Mass Loading, Mixing State, Size and Number in Present Day (2000) and Future (2100): Study with the Advanced Particle Microphysics (APM) module in the Community Earth System Model (CESM)

    NASA Astrophysics Data System (ADS)

    Luo, G.; Yu, F.

    2014-12-01

    Aerosols affect the global energy budget by scattering and absorbing sunlight (direct effects) and by changing the microphysical properties, lifetime, and coverage of clouds (indirect effects). One of the key challenges in quantifying the aerosol direct and indirect effects is to deep our understanding about the size distribution, size-resolved composition, and mixing state of aerosols. However, detailed information on size distribution and mixing state is often not available or incomplete in current climate models. Here, we incorporated APM into CESM. APM is a multi-type, multi-component (sulfate, nitrate, ammonium, SOA, BC, OC, dust, and sea salt), size-resolved particle microphysics model. Online chemistry, up-to-date nucleation, oxidation aging of medium-volatile and semi-volatile organic gases, aerosol-cloud interaction with stratiform cloud, shallow convection cloud, and deep convection cloud are considered. The amounts of secondary species coated on primary particles, through condensation, coagulation, equilibrium uptake, and aqueous chemistry, are also tracked. Model results are compared with aerosol mass observed by IMPROVE/EMEP, vertical structure of global particle number from aircraft-based field campaigns, particle and cloud condensation nuclei number at ground-based stations, aerosol optical properties retrieved by several satellites. Model results can capture the major characteristics shown in these observations. With this model system, we find that global burdens of sulfate, nitrate, ammonium, BC, OC from 2000 to 2100, under scenario RCP 4.5 where total radiative forcing is stabilized before 2100, are decreased by 44%, 50%, 43%, 40%, 40%, respectively. Dust and sea salt increase slightly. Global burdens of secondary species coated on BCOC, dust, and sea salt are deceased by 34%, 30% and 60%, respectively. Global averaged aerosol number in the lower troposphere (from surface to 3 km) is significantly decreased, especially for particles smaller than

  20. Aerosol processing in stratiform clouds in ECHAM6-HAM

    NASA Astrophysics Data System (ADS)

    Neubauer, David; Lohmann, Ulrike; Hoose, Corinna

    2013-04-01

    chemical components as well as 5 tracers for aerosol particles in ice crystals. This allows simulations of aerosol processing in warm, mixed-phase (e.g. through the Bergeron-Findeisen process) and ice clouds. The fixed scavenging ratios used for wet deposition in clouds in standard HAM are replaced by an explicit treatment of collision of cloud droplets/ice crystals with interstitial aerosol particles. Nucleation scavenging of aerosol particles by acting as cloud condensation nuclei or ice nuclei, freezing and evaporation of cloud droplets and melting and sublimation of ice crystals are treated explicitly. In extension to previous studies, aerosol particles from evaporating precipitation are released to modes which correspond to their size. Cloud processing of aerosol particles changes their size distribution and hence influences cloud droplet and ice crystal number concentrations as well as precipitation rate, which in turn affects aerosol concentrations. Results will be presented at the conference. Hoose et al., JGR, 2008a, doi: 10.1029/2007JD009251 Hoose et al., ACP, 2008b, doi: 10.5194/acp-8-6939-2008 Stevens et al., 2013, submitted Stier et al., ACP, 2005, doi: 10.5194/acp-5-1125-2005

  1. Search for D0-D0 mixing and branching-ratio measurement in the decay D0-->K+ pi- pi0.

    PubMed

    Aubert, B; Barate, R; Bona, M; Boutigny, D; Couderc, F; Karyotakis, Y; Lees, J P; Poireau, V; Tisserand, V; Zghiche, A; Grauges, E; Palano, A; Chen, J C; Qi, N D; Rong, G; Wang, P; Zhu, Y S; Eigen, G; Ofte, I; Stugu, B; Abrams, G S; Battaglia, M; Brown, D N; Button-Shafer, J; Cahn, R N; Charles, E; Gill, M S; Groysman, Y; Jacobsen, R G; Kadyk, J A; Kerth, L T; Kolomensky, Yu G; Kukartsev, G; Lynch, G; Mir, L M; Orimoto, T J; Pripstein, M; Roe, N A; Ronan, M T; Wenzel, W A; Del Amo Sanchez, P; Barrett, M; Ford, K E; Harrison, T J; Hart, A J; Hawkes, C M; Morgan, S E; Watson, A T; Held, T; Koch, H; Lewandowski, B; Pelizaeus, M; Peters, K; Schroeder, T; Steinke, M; Boyd, J T; Burke, J P; Cottingham, W N; Walker, D; Cuhadar-Donszelmann, T; Fulsom, B G; Hearty, C; Knecht, N S; Mattison, T S; McKenna, J A; Khan, A; Kyberd, P; Saleem, M; Sherwood, D J; Teodorescu, L; Blinov, V E; Bukin, A D; Druzhinin, V P; Golubev, V B; Onuchin, A P; Serednyakov, S I; Skovpen, Yu I; Solodov, E P; Todyshev, K Yu; Best, D S; Bondioli, M; Bruinsma, M; Chao, M; Curry, S; Eschrich, I; Kirkby, D; Lankford, A J; Lund, P; Mandelkern, M; Mommsen, R K; Roethel, W; Stoker, D P; Abachi, S; Buchanan, C; Foulkes, S D; Gary, J W; Long, O; Shen, B C; Wang, K; Zhang, L; Hadavand, H K; Hill, E J; Paar, H P; Rahatlou, S; Sharma, V; Berryhill, J W; Campagnari, C; Cunha, A; Dahmes, B; Hong, T M; Kovalskyi, D; Richman, J D; Beck, T W; Eisner, A M; Flacco, C J; Heusch, C A; Kroseberg, J; Lockman, W S; Nesom, G; Schalk, T; Schumm, B A; Seiden, A; Spradlin, P; Williams, D C; Wilson, M G; Albert, J; Chen, E; Dvoretskii, A; Fang, F; Hitlin, D G; Narsky, I; Piatenko, T; Porter, F C; Ryd, A; Samuel, A; Mancinelli, G; Meadows, B T; Mishra, K; Sokoloff, M D; Blanc, F; Bloom, P C; Chen, S; Ford, W T; Hirschauer, J F; Kreisel, A; Nagel, M; Nauenberg, U; Olivas, A; Ruddick, W O; Smith, J G; Ulmer, K A; Wagner, S R; Zhang, J; Chen, A; Eckhart, E A; Soffer, A; Toki, W H; Wilson, R J; Winklmeier, F; Zeng, Q; Altenburg, D D; Feltresi, E; Hauke, A; Jasper, H; Petzold, A; Spaan, B; Brandt, T; Klose, V; Lacker, H M; Mader, W F; Nogowski, R; Schubert, J; Schubert, K R; Schwierz, R; Sundermann, J E; Volk, A; Bernard, D; Bonneaud, G R; Grenier, P; Latour, E; Thiebaux, Ch; Verderi, M; Clark, P J; Gradl, W; Muheim, F; Playfer, S; Robertson, A I; Xie, Y; Andreotti, M; Bettoni, D; Bozzi, C; Calabrese, R; Cibinetto, G; Luppi, E; Negrini, M; Petrella, A; Piemontese, L; Prencipe, E; Anulli, F; Baldini-Ferroli, R; Calcaterra, A; de Sangro, R; Finocchiaro, G; Pacetti, S; Patteri, P; Peruzzi, I M; Piccolo, M; Rama, M; Zallo, A; Buzzo, A; Capra, R; Contri, R; Lo Vetere, M; Macri, M M; Monge, M R; Passaggio, S; Patrignani, C; Robutti, E; Santroni, A; Tosi, S; Brandenburg, G; Chaisanguanthum, K S; Morii, M; Wu, J; Dubitzky, R S; Marks, J; Schenk, S; Uwer, U; Bard, D J; Bhimji, W; Bowerman, D A; Dauncey, P D; Egede, U; Flack, R L; Nash, J A; Nikolich, M B; Panduro Vazquez, W; Behera, P K; Chai, X; Charles, M J; Mallik, U; Meyer, N T; Ziegler, V; Cochran, J; Crawley, H B; Dong, L; Eyges, V; Meyer, W T; Prell, S; Rosenberg, E I; Rubin, A E; Gritsan, A V; Denig, A G; Fritsch, M; Schott, G; Arnaud, N; Davier, M; Grosdidier, G; Höcker, A; Le Diberder, F; Lepeltier, V; Lutz, A M; Oyanguren, A; Pruvot, S; Rodier, S; Roudeau, P; Schune, M H; Stocchi, A; Wang, W F; Wormser, G; Cheng, C H; Lange, D J; Wright, D M; Chavez, C A; Forster, I J; Fry, J R; Gabathuler, E; Gamet, R; George, K A; Hutchcroft, D E; Payne, D J; Schofield, K C; Touramanis, C; Bevan, A J; Di Lodovico, F; Menges, W; Sacco, R; Cowan, G; Flaecher, H U; Hopkins, D A; Jackson, P S; McMahon, T R; Ricciardi, S; Salvatore, F; Wren, A C; Brown, D N; Davis, C L; Allison, J; Barlow, N R; Barlow, R J; Chia, Y M; Edgar, C L; Lafferty, G D; Naisbit, M T; Williams, J C; Yi, J I; Chen, C; Hulsbergen, W D; Jawahery, A; Lae, C K; Roberts, D A; Simi, G; Blaylock, G; Dallapiccola, C; Hertzbach, S S; Li, X; Moore, T B; Saremi, S; Staengle, H; Cowan, R; Sciolla, G; Sekula, S J; Spitznagel, M; Taylor, F; Yamamoto, R K; Kim, H; McLachlin, S E; Patel, P M; Robertson, S H; Lazzaro, A; Lombardo, V; Palombo, F; Bauer, J M; Cremaldi, L; Eschenburg, V; Godang, R; Kroeger, R; Sanders, D A; Summers, D J; Zhao, H W; Brunet, S; Côté, D; Simard, M; Taras, P; Viaud, F B; Nicholson, H; Cavallo, N; De Nardo, G; Fabozzi, F; Gatto, C; Lista, L; Monorchio, D; Paolucci, P; Piccolo, D; Sciacca, C; Baak, M; Raven, G; Snoek, H L; Jessop, C P; Losecco, J M; Allmendinger, T; Benelli, G; Gan, K K; Honscheid, K; Hufnagel, D; Jackson, P D; Kagan, H; Kass, R; Rahimi, A M; Ter-Antonyan, R; Wong, Q K; Blount, N L; Brau, J; Frey, R; Igonkina, O; Lu, M; Rahmat, R; Sinev, N B; Strom, D; Strube, J; Torrence, E; Gaz, A; Margoni, M; Morandin, M; Pompili, A; Posocco, M; Rotondo, M; Simonetto, F; Stroili, R; Voci, C; Benayoun, M; Chauveau, J; Briand, H; David, P; Del Buono, L; de la Vaissière, Ch; Hamon, O; Hartfiel, B L; John, M J J; Leruste, Ph; Malclès, J; Ocariz, J; Roos, L; Therin, G; Gladney, L; Panetta, J; Biasini, M; Covarelli, R; Angelini, C; Batignani, G; Bettarini, S; Bucci, F; Calderini, G; Carpinelli, M; Cenci, R; Forti, F; Giorgi, M A; Lusiani, A; Marchiori, G; Mazur, M A; Morganti, M; Neri, N; Paoloni, E; Rizzo, G; Walsh, J J; Haire, M; Judd, D; Wagoner, D E; Biesiada, J; Danielson, N; Elmer, P; Lau, Y P; Lu, C; Olsen, J; Smith, A J S; Telnov, A V; Bellini, F; Cavoto, G; D'Orazio, A; Del Re, D; Di Marco, E; Faccini, R; Ferrarotto, F; Ferroni, F; Gaspero, M; Li Gioi, L; Mazzoni, M A; Morganti, S; Piredda, G; Polci, F; Safai Tehrani, F; Voena, C; Ebert, M; Schröder, H; Waldi, R; Adye, T; De Groot, N; Franek, B; Olaiya, E O; Wilson, F F; Aleksan, R; Emery, S; Gaidot, A; Ganzhur, S F; Hamel de Monchenault, G; Kozanecki, W; Legendre, M; Vasseur, G; Yèche, Ch; Zito, M; Chen, X R; Liu, H; Park, W; Purohit, M V; Wilson, J R; Allen, M T; Aston, D; Bartoldus, R; Bechtle, P; Berger, N; Claus, R; Coleman, J P; Convery, M R; Cristinziani, M; Dingfelder, J C; Dorfan, J; Dubois-Felsmann, G P; Dujmic, D; Dunwoodie, W; Field, R C; Glanzman, T; Gowdy, S J; Graham, M T; Halyo, V; Hast, C; Hryn'ova, T; Innes, W R; Kelsey, M H; Kim, P; Leith, D W G S; Li, S; Luitz, S; Luth, V; Lynch, H L; Macfarlane, D B; Marsiske, H; Messner, R; Muller, D R; O'Grady, C P; Ozcan, V E; Perazzo, A; Perl, M; Pulliam, T; Ratcliff, B N; Roodman, A; Salnikov, A A; Schindler, R H; Schwiening, J; Snyder, A; Stelzer, J; Su, D; Sullivan, M K; Suzuki, K; Swain, S K; Thompson, J M; Va'vra, J; van Bakel, N; Weaver, M; Weinstein, A J R; Wisniewski, W J; Wittgen, M; Wright, D H; Yarritu, A K; Yi, K; Young, C C; Burchat, P R; Edwards, A J; Majewski, S A; Petersen, B A; Roat, C; Wilden, L; Ahmed, S; Alam, M S; Bula, R; Ernst, J A; Jain, V; Pan, B; Saeed, M A; Wappler, F R; Zain, S B; Bugg, W; Krishnamurthy, M; Spanier, S M; Eckmann, R; Ritchie, J L; Satpathy, A; Schilling, C J; Schwitters, R F; Izen, J M; Lou, X C; Ye, S; Bianchi, F; Gallo, F; Gamba, D; Bomben, M; Bosisio, L; Cartaro, C; Cossutti, F; Della Ricca, G; Dittongo, S; Lanceri, L; Vitale, L; Azzolini, V; Martinez-Vidal, F; Banerjee, Sw; Bhuyan, B; Brown, C M; Fortin, D; Hamano, K; Kowalewski, R; Nugent, I M; Roney, J M; Sobie, R J; Back, J J; Harrison, P F; Latham, T E; Mohanty, G B; Pappagallo, M; Band, H R; Chen, X; Cheng, B; Dasu, S; Datta, M; Flood, K T; Hollar, J J; Kutter, P E; Mellado, B; Mihalyi, A; Pan, Y; Pierini, M; Prepost, R; Wu, S L; Yu, Z; Neal, H

    2006-12-01

    We analyze 230.4 fb;{-1} of data collected with the BABAR detector at the PEP-II e;{+}e;{-} collider at SLAC to search for evidence of D0-D[over ];{0} mixing using regions of phase space in the decay D;{0}-->K;{+}pi;{-}pi;{0}. We measure the time-integrated mixing rate R_{M}=(0.023_{-0.014};{+0.018}(stat.)+/-0.004(syst.))%, and R_{M}<0.054% at the 95% confidence level, assuming CP invariance. The data are consistent with no mixing at the 4.5% confidence level. We also measure the branching ratio for D;{0}-->K;{+}pi;{-}pi;{0} relative to D;{0}-->K;{-}pi;{+}pi;{0} to be (0.214+/-0.008(stat.)+/-0.008(syst.))%.

  2. Multiple Flux Footprints, Flux Divergences and Boundary Layer Mixing Ratios: Studies of Ecosystem-Atmosphere CO2 Exchange Using the WLEF Tall Tower.

    NASA Astrophysics Data System (ADS)

    Davis, K. J.; Bakwin, P. S.; Yi, C.; Cook, B. D.; Wang, W.; Denning, A. S.; Teclaw, R.; Isebrands, J. G.

    2001-05-01

    Long-term, tower-based measurements using the eddy-covariance method have revealed a wealth of detail about the temporal dynamics of netecosystem-atmosphere exchange (NEE) of CO2. The data also provide a measure of the annual net CO2 exchange. The area represented by these flux measurements, however, is limited, and doubts remain about possible systematic errors that may bias the annual net exchange measurements. Flux and mixing ratio measurements conducted at the WLEF tall tower as part of the Chequamegon Ecosystem-Atmosphere Study (ChEAS) allow for unique assessment of the uncertainties in NEE of CO2. The synergy between flux and mixing ratio observations shows the potential for comparing inverse and eddy-covariance methods of estimating NEE of CO2. Such comparisons may strengthen confidence in both results and begin to bridge the huge gap in spatial scales (at least 3 orders of magnitude) between continental or hemispheric scale inverse studies and kilometer-scale eddy covariance flux measurements. Data from WLEF and Willow Creek, another ChEAS tower, are used to estimate random and systematic errors in NEE of CO2. Random uncertainty in seasonal exchange rates and the annual integrated NEE, including both turbulent sampling errors and variability in enviromental conditions, is small. Systematic errors are identified by examining changes in flux as a function of atmospheric stability and wind direction, and by comparing the multiple level flux measurements on the WLEF tower. Nighttime drainage is modest but evident. Systematic horizontal advection occurs during the morning turbulence transition. The potential total systematic error appears to be larger than random uncertainty, but still modest. The total systematic error, however, is difficult to assess. It appears that the WLEF region ecosystems were a small net sink of CO2 in 1997. It is clear that the summer uptake rate at WLEF is much smaller than that at most deciduous forest sites, including the nearby

  3. Aerosol vertical distribution and optical properties over China from long-term satellite and ground-based remote sensing

    NASA Astrophysics Data System (ADS)

    Tian, Pengfei; Cao, Xianjie; Zhang, Lei; Sun, Naixiu; Sun, Lu; Logan, Timothy; Shi, Jinsen; Wang, Yuan; Ji, Yuemeng; Lin, Yun; Huang, Zhongwei; Zhou, Tian; Shi, Yingying; Zhang, Renyi

    2017-02-01

    The seasonal and spatial variations of vertical distribution and optical properties of aerosols over China are studied using long-term satellite observations from the Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP) and ground-based lidar observations and Aerosol Robotic Network (AERONET) data. The CALIOP products are validated using the ground-based lidar measurements at the Semi-Arid Climate and Environment Observatory of Lanzhou University (SACOL). The Taklamakan Desert and Tibetan Plateau regions exhibit the highest depolarization and color ratios because of the natural dust origin, whereas the North China Plain, Sichuan Basin and Yangtze River Delta show the lowest depolarization and color ratios because of aerosols from secondary formation of the anthropogenic origin. Certain regions, such as the North China Plain in spring and the Loess Plateau in winter, show intermediate depolarization and color ratios because of mixed dust and anthropogenic aerosols. In the Pearl River Delta region, the depolarization and color ratios are similar to but higher than those of the other polluted regions because of combined anthropogenic and marine aerosols. Long-range transport of dust in the middle and upper troposphere in spring is well captured by the CALIOP observations. The seasonal variations in the aerosol vertical distributions reveal efficient transport of aerosols from the atmospheric boundary layer to the free troposphere because of summertime convective mixing. The aerosol extinction lapse rates in autumn and winter are more positive than those in spring and summer, indicating trapped aerosols within the boundary layer because of stabler meteorological conditions. More than 80 % of the column aerosols are distributed within 1.5 km above the ground in winter, when the aerosol extinction lapse rate exhibits a maximum seasonal average in all study regions except for the Tibetan Plateau. The aerosol extinction lapse rates in the polluted regions are higher

  4. Chemical composition of the atmospheric aerosol in the troposphere over the Hudson Bay lowlands and Quebec-Labrador regions of Canada

    NASA Astrophysics Data System (ADS)

    Gorzelska, K.; Talbot, R. W.; Klemm, K.; Lefer, B.; Klemm, O.; Gregory, G. L.; Anderson, B.; Barrie, L. A.

    1994-01-01

    Atmospheric aerosols were collected in the boundary layer and free troposphere over continental and coastal subarctic regions of Canada during the July-August 1990 joint U.S.-Canadian Arctic Boundary Layer Expedition (ABLE) SB/Northern Wetlands Study (NOWES). The samples were analyzed for the following water soluble species: sulfate, nitrate, ammonium, potassium, sodium, chloride, oxalate, methylsulfonate, and total amine nitrogen. Ammonium and sulfate were the major water soluble components of these aerosols. The nearly neutral (overall) chemical composition of summertime aerosol particles contrasts their strongly acidic wintertime composition. Aerosol samples were separated into several air mass categories and characterized in terms of chemical composition, associated mixing ratios of gaseous compounds, and meteorological parameters. The fundamental category represented particles associated with"background"air masses. The summertime atmospheric aerosols in background air over the North American subarctic and Arctic regions were characterized by relatively small and spatially uniform mixing ratios of the measured species. These aerosol particles were aged to the extent that they had lost their primary source signature. The chemical profile of the background air aerosols was frequently modified by additions from biomass fire plumes, aged tropical marine air, and intrusions of upper tropospheric/lower stratospheric air. Aerosols in boundary layer background air over the boreal forested region of Quebec-Labrador had significantly larger mixing ratios of ammonium and sulfate relative to the Hudson Bay region. This may reflect infiltration of anthropogenic pollution or be due to natural emissions from this region.

  5. Chemical composition of the atmospheric aerosol in the troposphere over the Hudson Bay lowlands and Quebec-Labrador regions of Canada

    NASA Technical Reports Server (NTRS)

    Gorzelska, K.; Talbot, R. W.; Klemm, K.; Lefer, B.; Klemm, O.; Gregory, G. L.; Anderson, B.; Barrie, L. A.

    1994-01-01

    Atmospheric aerosols were collected in the boundary layer and free troposphere over continental and coastal subarctic regions of Canada during the July - August 1990 joint U.S.-Canadian Arctic Boundary Layer Expedition (ABLE) 3B/Northern Wetlands Study (NOWES). The samples were analyzed for the following water soluble species: sulfate, nitrate, ammonium, potassium, sodium, chloride, oxalate, methylsulfonate, and total amine nitrogen. Ammonium and sulfate were the major water soluble components of these aerosols. The nearly neutral (overall) chemical composition of summertime aerosol particles contrasts their strongly acidic wintertime composition. Aerosol samples were separated into several air mass categories and characterized in terms of chemical composition, associated mixing ratios of gaseous compounds, and meteorological parameters. The fundamental category represented particles associated with 'background' air masses. The summertime atmospheric aerosols in background air over the North American subarctic and Arctic regions were characterized by relatively small and spatially uniform mixing ratios of the measured species. These aerosol particles were aged to the extent that they had lost their primary source signature. The chemical profile of the background air aerosols was frequently modified by additions from biomass fire plumes, aged tropical marine air, and intrusions of upper tropospheric/lower stratospheric air. Aerosols in boundary layer background air over the boreal forest region of Quebec-Labrador had significantly larger mixing ratios of ammonium and sulfate relative to the Hudson Bay region. This may reflect infiltration of anthropogenic pollution or be due to natural emissions from this region.