Science.gov

Sample records for aerosol extinction spectroscopy

  1. Optical and Physicochemical Properties of Brown Carbon Aerosol: Light Scattering, FTIR Extinction Spectroscopy, and Hygroscopic Growth.

    PubMed

    Tang, Mingjin; Alexander, Jennifer M; Kwon, Deokhyeon; Estillore, Armando D; Laskina, Olga; Young, Mark A; Kleiber, Paul D; Grassian, Vicki H

    2016-06-23

    A great deal of attention has been paid to brown carbon aerosol in the troposphere because it can both scatter and absorb solar radiation, thus affecting the Earth's climate. However, knowledge of the optical and chemical properties of brown carbon aerosol is still limited. In this study, we have investigated different aspects of the optical properties of brown carbon aerosol that have not been previously explored. These properties include extinction spectroscopy in the mid-infrared region and light scattering at two different visible wavelengths, 532 and 402 nm. A proxy for atmospheric brown carbon aerosol was formed from the aqueous reaction of ammonium sulfate with methylglyoxal. The different optical properties were measured as a function of reaction time for a period of up to 19 days. UV/vis absorption experiments of bulk solutions showed that the optical absorption of aqueous brown carbon solution significantly increases as a function of reaction time in the spectral range from 200 to 700 nm. The analysis of the light scattering data, however, showed no significant differences between ammonium sulfate and brown carbon aerosol particles in the measured scattering phase functions, linear polarization profiles, or the derived real parts of the refractive indices at either 532 or 402 nm, even for the longest reaction times with greatest visible extinction. The light scattering experiments are relatively insensitive to the imaginary part of the refractive index, and it was only possible to place an upper limit of k ≤ 0.01 on the imaginary index values. These results suggest that after the reaction with methylglyoxal the single scattering albedo of ammonium sulfate aerosol is significantly reduced but that the light scattering properties including the scattering asymmetry parameter, which is a measure of the relative amount of forward-to-backward scattering, remain essentially unchanged from that of unprocessed ammonium sulfate. The optical extinction properties

  2. Measurements of extinction by aerosol particles in the near-infrared using continuous wave cavity ring-down spectroscopy.

    PubMed

    Mellon, Daniel; King, Simon J; Kim, Jin; Reid, Jonathan P; Orr-Ewing, Andrew J

    2011-02-10

    Cavity ring-down spectroscopy using a fiber-coupled continuous wave distributed feedback laser at a wavelength of 1520 nm has been used to measure extinction of light by samples of nearly monodisperse aerosol particles <1 μm in diameter. A model is tested for the analysis of the sample extinction that is based on the Poisson statistics of the number of particles within the intracavity laser beam: variances of measured extinction are used to derive values of the scattering cross section for size-selected aerosol particles, without need for knowledge of the particle number density or sample length. Experimental parameters that influence the performance of the CRD system and the application and limitations of the statistical model are examined in detail. Determinations are reported of the scattering cross sections for polystyrene spheres (PSSs), sodium chloride, and ammonium sulfate, and, for particles greater than 500 nm in diameter, are shown to be in agreement with the corresponding values calculated using Mie theory or Discrete Dipole Approximation methods. For smaller particles, the experimentally derived values of the scattering cross section are larger than the theoretical predictions, and transmission of a small fraction of larger particles into the cavity is argued to be responsible for this discrepancy. The effects of cubic structure on the determination of optical extinction efficiencies of sodium chloride aerosol particles are examined. Values are reported for the real components of the refractive indices at 1520 nm of PSS, sodium chloride, and ammonium sulfate aerosol particles.

  3. Infrared spectroscopy of aerosols

    NASA Astrophysics Data System (ADS)

    Mentel, Th.; Sebald, H.

    2003-04-01

    In our large Aerosol Chamber at the FZ Jülich we apply HR FTIR absorption spectroscopy for the determination of trace gases. In the FTIR spectra we also observe broad absorptions of several 10 to a few 100 cm-1 widths that arise from species in the condensed aerosol phase: liquid H_2O, NO_3^-, SO_42-, HSO_4^-, or dicarboxylic acids. Moreover, the aerosol droplets caused extinctions over several 1000 cm-1 by IR scattering. This allows for in-situ observation of changes in the condensed aerosol phase e.g. on HNO_3 uptake, like the shift of the sulfate/bisulfate equilibrium or the growth by water condensation. The IR absorptions of the condensed aerosol phase provide useful extra information in process studies, if they can be quantified. Therefore the absorption cross section, respective, the absorption index which is the imaginary part of the complex refractive index is needed. We set up an aerosol flow tube in which IR spectroscopy on a 8 m light path and aerosol size distribution measurements in the range from 20 nm - 10 μm can be performed simultaneously. We measured sulfate aerosols at several relative humidities (dry, metastable, deliquescent). We will demonstrate an iterative procedure based on Mie calculations and Kramers Kronig transformation to retrieve the absorption index from the observed IR spectra and the corresponding size distribution (for dry ammonium sulfate). We will compare resulting absorption indices for aqueous sodium bisulfate aerosols at several relative humidties with thermodynamic model calculations for the Na^+/H^+/HSO_4^-/SO_42-/H_2O system.

  4. Single nanowire extinction spectroscopy.

    PubMed

    Giblin, Jay; Vietmeyer, Felix; McDonald, Matthew P; Kuno, Masaru

    2011-08-10

    Here we show the first direct extinction spectra of single one-dimensional (1D) semiconductor nanostructures obtained at room temperature utilizing a spatial modulation approach. (1) For these materials, ensemble averaging in conventional extinction spectroscopy has limited our understanding of the interplay between carrier confinement and their electrostatic interactions. (2-4) By probing individual CdSe nanowires (NWs), we have identified and assigned size-dependent exciton transitions occurring across the visible. In turn, we have revealed the existence of room temperature 1D excitons in the narrowest NWs.

  5. Broadband measurements of aerosol extinction in the ultraviolet spectral region

    NASA Astrophysics Data System (ADS)

    Washenfelder, R. A.; Flores, J. M.; Brock, C. A.; Brown, S. S.; Rudich, Y.

    2013-01-01

    Aerosols influence the Earth's radiative budget by scattering and absorbing incoming solar radiation. The optical properties of aerosols vary as a function of wavelength, but few measurements have reported the wavelength dependence of aerosol extinction cross-sections and complex refractive indices. We describe a new laboratory instrument to measure aerosol optical extinction as a function of wavelength, using cavity enhanced spectroscopy with a broadband light source. The instrument consists of two broadband channels which span the 360-390 and 385-420 nm spectral regions using two light emitting diodes (LED) and a grating spectrometer with charge-coupled device (CCD) detector. We determined aerosol extinction cross-sections and directly observed Mie scattering resonances for aerosols that are purely scattering (polystyrene latex spheres and ammonium sulfate), slightly absorbing (Suwannee River fulvic acid), and strongly absorbing (nigrosin dye). We describe an approach for retrieving refractive indices as a function of wavelength from the measured extinction cross-sections over the 360-420 nm wavelength region. The retrieved refractive indices for PSL and ammonium sulfate agree within uncertainty with literature values for this spectral region. The refractive index determined for nigrosin is 1.78 (±0.03) + 0.19 (±0.08) i at 360 nm and 1.53 (±0.03) + 0.21 (±0.05) i at 420 nm. The refractive index determined for Suwannee River fulvic acid is 1.71 (±0.02) + 0.07 (±0.06) i at 360 nm and 1.66 (±0.02) + 0.06 (±0.04) i at 420 nm. These laboratory results support the potential for a field instrument capable of determining ambient aerosol optical extinction, average aerosol extinction cross-section, and complex refractive index as a function of wavelength.

  6. Broadband measurements of aerosol extinction in the ultraviolet spectral region

    NASA Astrophysics Data System (ADS)

    Washenfelder, R. A.; Flores, J. M.; Brock, C. A.; Brown, S. S.; Rudich, Y.

    2013-04-01

    Aerosols influence the Earth's radiative budget by scattering and absorbing incoming solar radiation. The optical properties of aerosols vary as a function of wavelength, but few measurements have reported the wavelength dependence of aerosol extinction cross sections and complex refractive indices. We describe a new laboratory instrument to measure aerosol optical extinction as a function of wavelength, using cavity enhanced spectroscopy with a broadband light source. The instrument consists of two broadband channels which span the 360-390 and 385-420 nm spectral regions using two light emitting diodes (LED) and a grating spectrometer with charge-coupled device (CCD) detector. We determined aerosol extinction cross sections and directly observed Mie scattering resonances for aerosols that are purely scattering (polystyrene latex spheres and ammonium sulfate), slightly absorbing (Suwannee River fulvic acid), and strongly absorbing (nigrosin dye). We describe an approach for retrieving refractive indices as a function of wavelength from the measured extinction cross sections over the 360-420 nm wavelength region. The retrieved refractive indices for PSL and ammonium sulfate agree within uncertainty with the literature values for this spectral region. The refractive index determined for nigrosin is 1.78 (± 0.03) + 0.19 (± 0.08)i at 360 nm and 1.63 (± 0.03) + 0.21 (± 0.05)i at 420 nm. The refractive index determined for Suwannee River fulvic acid is 1.71 (± 0.02) + 0.07 (± 0.06)i at 360 nm and 1.66 (± 0.02) + 0.06 (± 0.04)i at 420 nm. These laboratory results support the potential for a field instrument capable of determining ambient aerosol optical extinction, average aerosol extinction cross section, and complex refractive index as a function of wavelength.

  7. Humidity Dependent Extinction of Clay Aerosols

    NASA Astrophysics Data System (ADS)

    Greenslade, M. E.; Attwood, A. R.

    2010-12-01

    Aerosols play an important role in the Earth’s radiative balance by directly scattering and absorbing radiation. The magnitude of aerosol forcing can be altered by changes in relative humidity which cause aerosol size, shape and refractive index to vary. To quantify these effects, a custom cavity ring down instrument operated at 532 nm with two sample channels measures aerosols extinction under dry conditions and at elevated humidity. The optical growth, fRH(ext), is determined as a ratio of the extinction cross section at high relative humidity to that under dry conditions. Three key clay components of mineral dust and mixtures of clay components with ammonium sulfate are investigated using this method. Experimentally obtained optical growth is compared with physical growth factors from the literature and our work determined using several different techniques. Further, Mie theory calculations based on published optical constants are compared with experimental results. Differences between theory and experiment will be discussed.

  8. Intercomparison of aerosol extinction profiles retrieved from MAX-DOAS measurements

    NASA Astrophysics Data System (ADS)

    Frieß, U.; Klein Baltink, H.; Beirle, S.; Clémer, K.; Hendrick, F.; Henzing, B.; Irie, H.; de Leeuw, G.; Li, A.; Moerman, M. M.; van Roozendael, M.; Shaiganfar, R.; Wagner, T.; Wang, Y.; Xie, P.; Yilmaz, S.; Zieger, P.

    2016-07-01

    A first direct intercomparison of aerosol vertical profiles from Multi-Axis Differential Optical Absorption Spectroscopy (MAX-DOAS) observations, performed during the Cabauw Intercomparison Campaign of Nitrogen Dioxide measuring Instruments (CINDI) in summer 2009, is presented. Five out of 14 participants of the CINDI campaign reported aerosol extinction profiles and aerosol optical thickness (AOT) as deduced from observations of differential slant column densities of the oxygen collision complex (O4) at different elevation angles. Aerosol extinction vertical profiles and AOT are compared to backscatter profiles from a ceilometer instrument and to sun photometer measurements, respectively. Furthermore, the near-surface aerosol extinction coefficient is compared to in situ measurements of a humidity-controlled nephelometer and dry aerosol absorption measurements. The participants of this intercomparison exercise use different approaches for the retrieval of aerosol information, including the retrieval of the full vertical profile using optimal estimation and a parametrised approach with a prescribed profile shape. Despite these large conceptual differences, and also differences in the wavelength of the observed O4 absorption band, good agreement in terms of the vertical structure of aerosols within the boundary layer is achieved between the aerosol extinction profiles retrieved by the different groups and the backscatter profiles observed by the ceilometer instrument. AOTs from MAX-DOAS and sun photometer show a good correlation (R>0.8), but all participants systematically underestimate the AOT. Substantial differences between the near-surface aerosol extinction from MAX-DOAS and from the humidified nephelometer remain largely unresolved.

  9. Photothermal spectroscopy of aerosols

    SciTech Connect

    Campillo, A.J.; Lin, H.B.

    1981-04-01

    In situ aerosol absorption spectroscopy was performed using two novel photothermal detection schemes. The first, based on a photorefractive effect and coherent detection, called phase fluctuation optical heterodyne (PFLOH) spectroscopy, could, depending on the geometry employed, yield particle specific or particle and gas absorption data. Single particles of graphite as small as 1 ..mu..m were detected in the particle specific mode. In another geometrical configuration, the total absorption (both gas and particle) of submicron sized aerosols of ammonium sulfate particles in equilibrium with gaseous ammonia and water vapor were measured at varying CO/sub 2/ laser frequencies. The specific absorption coefficient for the sulfate ion was measured to be 0.5 m/sup 2//g at 1087 cm/sup -1/. The absorption coefficient sensitivity of this scheme was less than or equal to 10/sup -8/ cm/sup -1/. The second scheme is a hybrid visible Mie scattering scheme incorporating photothermal modulation. Particle specific data on ammonium sulfate droplets were obtained. For chemically identical species, the relative absorption spectrum versus laser frequency can be obtained for polydisperse aerosol distributions directly from the data without the need for complex inverse scattering calculations.

  10. Mid-infrared extinction by sulfate aerosols from the Mt. Pinatubo eruption

    NASA Technical Reports Server (NTRS)

    Rinsland, C. P.; Yue, G. K.; Gunson, M. R.; Zander, R.; Abrams, M. C.

    1994-01-01

    Quantitative measurements of the wavelength dependence of aerosol extinction in the 750-3400/cm spectral region have been derived from 0.01/cm resolution stratospheric solar occultation spectra recorded by the ATMOS (Atmospheric Trace Molecule Spectroscopy) Fourier transform spectrometer about 9 1/2 months after the Mt Pinatubo volcanic eruption. Strong, broad aerosol features have been identified near 900, 1060, 1190, 1720, and 2900/cm below a tangent height of approximately 30 km. Aerosol extinction measurements derived from approximately 0.05/cm wide microwindows nearly free of telluric line absorption in the ATMOS spectra are compared with transmission calculations derived from aerosol size distribution profiles retrieved from correlative SAGE (Stratospheric Aerosol and Gas Experiment) II visible and near i.r. extinction measurements, seasonal and zonally averaged H2SO4 aerosol weight percentage profiles, and published sulfuric acid optical constants derived from room temperature laboratory measurements. The calculated shapes and positions of the aerosol features are generally consistent with the observations, thereby confirming that the aerosols are predominantly concentrated H2SO4-H2O droplets, but there are significant differences between the measured and calculated wavelength dependences of the aerosol extinction. We attribute these differences as primarily the result of errors in the calculated low temperature H2SO4-H2O optical constants. Errors in both the published room temperature optical constants and the limitations of the Lorentz-Lorenz relation are likely to be important.

  11. Field Studies of Broadband Aerosol Optical Extinction in the Ultraviolet Spectral Region

    NASA Astrophysics Data System (ADS)

    Washenfelder, R. A.; Attwood, A.; Brock, C. A.; Brown, S. S.

    2013-12-01

    Aerosols influence the Earth's radiative budget by scattering and absorbing incoming solar radiation. The optical properties of aerosols vary as a function of wavelength, but few measurements have reported the wavelength dependence of aerosol extinction cross sections and complex refractive indices. In the case of brown carbon, its wavelength-dependent absorption in the ultraviolet spectral region has been suggested as an important component of aerosol radiative forcing. We describe a new field instrument to measure aerosol optical extinction as a function of wavelength, using cavity enhanced spectroscopy with a broadband light source. The instrument consists of two broadband channels which span the 360-390 and 385-420 nm spectral regions using two light emitting diodes (LED) and a grating spectrometer with charge-coupled device (CCD) detector. We deployed this instrument during the Fire Lab at Missoula Experiment during Fall 2012 to measure biomass burning aerosol, and again during the Southern Oxidant and Aerosol Study in summer 2013 to measure organic aerosol in the Southeastern U.S. In both field experiments, we determined aerosol optical extinction as a function of wavelength and can interpret this together with size distribution and composition measurements to characterize the aerosol optical properties and radiative forcing.

  12. Mount St. Helens related aerosol properties from solar extinction measurements

    SciTech Connect

    Michalsky, J.J.; Kleckner, E.W.; Stokes, G.M.

    1980-11-01

    The optical extinction due to the introduction of aerosols and aerosol-precursors into the troposphere and stratosphere during the major eruptive phase of Mount St. Helens, Washington, is quantified. The concentration is on the two-week period centered on the major eruption of 22 July 1980. (ACR)

  13. Interpretation of solar extinction data for stratospheric aerosols

    NASA Technical Reports Server (NTRS)

    Pepin, T. J.

    1980-01-01

    This paper discusses the inversion problem for aerosols using the solar extinction method. A series of numerical experiments is described in which solar extinction measurement systems are modeled. A numerical model of a solar extinction measurement system has been coupled with model atmospheres that exhibit fine scale structures to produce numerically generated data signals. These signals were then inverted to study the effect that measurement errors and desired vertical resolution produce in the inverted results. Knowledge o2 the trade off between vertical resolution and the accuracy of inversion aid in the interpretation of the inverted results.

  14. Recent Improvements to CALIOP Level 3 Aerosol Profile Product for Global 3-D Aerosol Extinction Characterization

    NASA Astrophysics Data System (ADS)

    Tackett, J. L.; Getzewich, B. J.; Winker, D. M.; Vaughan, M. A.

    2015-12-01

    With nine years of retrievals, the CALIOP level 3 aerosol profile product provides an unprecedented synopsis of aerosol extinction in three dimensions and the potential to quantify changes in aerosol distributions over time. The CALIOP level 3 aerosol profile product, initially released as a beta product in 2011, reports monthly averages of quality-screened aerosol extinction profiles on a uniform latitude/longitude grid for different cloud-cover scenarios, called "sky conditions". This presentation demonstrates improvements to the second version of the product which will be released in September 2015. The largest improvements are the new sky condition definitions which parse the atmosphere into "cloud-free" views accessible to passive remote sensors, "all-sky" views accessible to active remote sensors and "cloudy-sky" views for opaque and transparent clouds which were previously inaccessible to passive remote sensors. Taken together, the new sky conditions comprehensively summarize CALIOP aerosol extinction profiles for a broad range of scientific queries. In addition to dust-only extinction profiles, the new version will include polluted-dust and smoke-only extinction averages. A new method is adopted for averaging dust-only extinction profiles to reduce high biases which exist in the beta version of the level 3 aerosol profile product. This presentation justifies the new averaging methodology and demonstrates vertical profiles of dust and smoke extinction over Africa during the biomass burning season. Another crucial advancement demonstrated in this presentation is a new approach for computing monthly mean aerosol optical depth which removes low biases reported in the beta version - a scenario unique to lidar datasets.

  15. MAX-DOAS retrieval of aerosol extinction properties in Madrid, Spain

    NASA Astrophysics Data System (ADS)

    Wang, Shanshan; Cuevas, Carlos A.; Frieß, Udo; Saiz-Lopez, Alfonso

    2016-10-01

    Multi-axis differential optical absorption spectroscopy (MAX-DOAS) measurements were performed in the urban environment of Madrid, Spain, from March to September 2015. The O4 absorption in the ultraviolet (UV) spectral region was used to retrieve the aerosol extinction profile using an inversion algorithm. The results show a good agreement between the hourly retrieved aerosol optical depth (AOD) and the correlative Aerosol Robotic Network (AERONET) product, with a correlation coefficient of R = 0.87. Higher AODs are found in the summer season due to the more frequent occurrence of Saharan dust intrusions. The surface aerosol extinction coefficient as retrieved by the MAX-DOAS measurements was also compared to in situ PM2.5 concentrations. The level of agreement between both measurements indicates that the MAX-DOAS retrieval has the ability to characterize the extinction of aerosol particles near the surface. The retrieval algorithm was also used to study a case of severe dust intrusion on 12 May 2015. The capability of the MAX-DOAS retrieval to recognize the dust event including an elevated particle layer is investigated along with air mass back-trajectory analysis.

  16. Improvement of Raman lidar algorithm for quantifying aerosol extinction

    NASA Technical Reports Server (NTRS)

    Russo, Felicita; Whiteman, David; Demoz, Belay; Hoff, Raymond

    2005-01-01

    Aerosols are particles of different composition and origin and influence the formation of clouds which are important in atmospheric radiative balance. At the present there is high uncertainty on the effect of aerosols on climate and this is mainly due to the fact that aerosol presence in the atmosphere can be highly variable in space and time. Monitoring of the aerosols in the atmosphere is necessary to better understanding many of these uncertainties. A lidar (an instrument that uses light to detect the extent of atmospheric aerosol loading) can be particularly useful to monitor aerosols in the atmosphere since it is capable to record the scattered intensity as a function of altitude from molecules and aerosols. One lidar method (the Raman lidar) makes use of the different wavelength changes that occur when light interacts with the varying chemistry and structure of atmospheric aerosols. One quantity that is indicative of aerosol presence is the aerosol extinction which quantifies the amount of attenuation (removal of photons), due to scattering, that light undergoes when propagating in the atmosphere. It can be directly measured with a Raman lidar using the wavelength dependence of the received signal. In order to calculate aerosol extinction from Raman scattering data it is necessary to evaluate the rate of change (derivative) of a Raman signal with respect to altitude. Since derivatives are defined for continuous functions, they cannot be performed directly on the experimental data which are not continuous. The most popular technique to find the functional behavior of experimental data is the least-square fit. This procedure allows finding a polynomial function which better approximate the experimental data. The typical approach in the lidar community is to make an a priori assumption about the functional behavior of the data in order to calculate the derivative. It has been shown in previous work that the use of the chi-square technique to determine the most

  17. Applications of Sunphotometry to Aerosol Extinction and Surface Anisotropy

    SciTech Connect

    Tsay, S.

    2002-09-30

    Support cost-sharing of a newly developed sunphotometer in field deployment for aerosol studies. This is a cost-sharing research to deploy a newly developed sun-sky-surface photometer for studying aerosol extinction and surface anisotropy at the ARM SGP, TWP, and NSA-AAO CART sites and in many field campaigns. Atmospheric aerosols affect the radiative energy balance of the Earth, both directly by perturbing the incoming/outgoing radiation fields and indirectly by influencing the properties/processes of clouds and reactive greenhouse gases. The surface bidirectional reflectance distribution function (BRDF) also plays a crucial role in the radiative energy balance, since the BRDF is required to determine (i) the spectral and spectrally-averaged surface albedo, and (ii) the top-of-the-atmosphere (TOA) angular distribution of radiance field. Therefore, the CART sites provide an excellent, albeit unique, opportunity to collect long-term climatic data in characterizing aerosol properties and various types of surface anisotropy.

  18. Applications of Sunphotometry to Aerosol Extinction and Surface Anisotropy

    NASA Technical Reports Server (NTRS)

    Tsay, S. C.; Holben, B. N.; Privette, J. L.

    2005-01-01

    Support cost-sharing of a newly developed sunphotometer in field deployment for aerosol studies. This is a cost-sharing research to deploy a newly developed sun-sky-surface photometer for studying aerosol extinction and surface anisotropy at the ARM SGP, TWP, and NSA-AAO CART sites and in many field campaigns. Atmospheric aerosols affect the radiative energy balance of the Earth, both directly by perturbing the incoming/outgoing radiation fields and indirectly by influencing the properties/processes of clouds and reactive greenhouse gases. The surface bidirectional reflectance distribution function (BRDF) also plays a crucial role in the radiative energy balance, since the BRDF is required to determine (1) the spectral and spectrally-averaged surface albedo, and (2) the top-of-the-atmosphere (TOA) angular distribution of radiance field. Therefore, the CART sites provide an excellent, albeit unique, opportunity to collect long-term climatic data in characterizing aerosol properties and various types of surface anisotropy.

  19. Aerosol and Light Extinction Databases for North America and Europe

    DTIC Science & Technology

    1992-06-10

    Light Extinction Database ........................................... 5 2.3 NPS - NFPN Aerosol Chemestry Database...E. Wilson of U.S. Environmental Protection Agency, co-operative agreement # CR-81-5727-02-0. His help is greatly appreciated. The NESCAUM data were...Environment 11: 803-812. 8. EPA Report to Congress, 1979. Protecting Visibility. Environmental Protection Agency, Report No. EPA-450/5-79-008. 9. Husar, R. B

  20. Measurement of size-dependent single scattering albedo of fresh biomass burning aerosols using the extinction-minus-scattering technique with a combination of cavity ring-down spectroscopy and nephelometry

    NASA Astrophysics Data System (ADS)

    Singh, Sujeeta; Fiddler, Marc N.; Bililign, Solomon

    2016-11-01

    Biomass burning (BB) aerosols have a significant effect on regional climate, and represent a significant uncertainty in our understanding of climate change. Using a combination of cavity ring-down spectroscopy and integrating nephelometry, the single scattering albedo (SSA) and Ångstrom absorption exponent (AAE) were measured for several North American biomass fuels. This was done for several particle diameters for the smoldering and flaming stage of white pine, red oak, and cedar combustion. Measurements were done over a wider wavelength range than any previous direct measurement of BB particles. While the offline sampling system used in this work shows promise, some changes in particle size distribution were observed, and a thorough evaluation of this method is required. The uncertainty of SSA was 6 %, with the truncation angle correction of the nephelometer being the largest contributor to error. While scattering and extinction did show wavelength dependence, SSA did not. SSA values ranged from 0.46 to 0.74, and were not uniformly greater for the smoldering stage than the flaming stage. SSA values changed with particle size, and not systematically so, suggesting the proportion of tar balls to fractal black carbon change with fuel type/state and particle size. SSA differences of 0.15-0.4 or greater can be attributed to fuel type or fuel state for fresh soot. AAE values were quite high (1.59-5.57), despite SSA being lower than is typically observed in wildfires. The SSA and AAE values in this work do not fit well with current schemes that relate these factors to the modified combustion efficiency of a burn. Combustion stage, particle size, fuel type, and fuel condition were found to have the most significant effects on the intrinsic optical properties of fresh soot, though additional factors influence aged soot.

  1. Airborne Cavity Ring-Down Measurement of Aerosol Extinction and Scattering During the Aerosol IOP

    NASA Technical Reports Server (NTRS)

    Strawa, A. W.; Ricci, K.; Provencal, R.; Schmid, B.; Covert, D.; Elleman, R.; Arnott, P.

    2003-01-01

    Large uncertainties in the effects of aerosols on climate require improved in-situ measurements of extinction coefficient and single-scattering albedo. This paper describes preliminary results from Cadenza, a new continuous wave cavity ring-down (CW-CRD) instrument designed to address these uncertainties. Cadenza measures the aerosol extinction coefficient for 675 nm and 1550 nm light, and simultaneously measures the scattering coefficient at 675 nm. In the past year Cadenza was deployed in the Asian Dust Above Monterey (ADAM) and DOE Aerosol Intensive Operating Period (IOP) field projects. During these flights Cadenza produced measurements of aerosol extinction in the range from 0.2 to 300 Mm-1 with an estimated precision of 0.1 Min-1 for 1550 nm light and 0.2 Mm-1 for 675 nm light. Cadenza data from the ADAM and Aerosol IOP missions compared favorably with data from the other instruments aboard the CIRPAS Twin Otter aircraft and participating in those projects.= We present comparisons between the Cadenza measurements and those friom a TSI nephelometer, Particle Soot Absorption Photometer (PSAP), and the AATS 14 sun-photometer. Measurements of the optical properties of smoke and dust plumes sampled during these campaigns are presented and estimates of heating rates due to these plumes are made.

  2. Comparison of aerosol extinction profiles from lidar and SAGE II data at a tropical station

    NASA Technical Reports Server (NTRS)

    Parameswaran, K.; Rose, K. O.; Murthy, B. V. K.; Osborn, M. T.; Mcmaster, L. R.

    1991-01-01

    Aerosol extinction profiles obtained from lidar data at Trivandrum (8.6 deg N, 77 deg E) are compared with corresponding Stratospheric Aerosol and Gas Experiment II extinction profiles. The agreement between the two is found to be satisfactory. The extinction profiles obtained by both the experiments showed a prominent peak at 23-24 km altitude in the stratosphere. The study revealed large variability in upper tropospheric extinction with location (latitude).

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

    NASA Technical Reports Server (NTRS)

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

    1984-01-01

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

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

    NASA Technical Reports Server (NTRS)

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

    1989-01-01

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

  5. Two-Column Aerosol Project: Aerosol Light Extinction Measurements Field Campaign Report

    SciTech Connect

    Dubey, Manvendra; Aiken, Allison; Berg, Larry K.; Freedman, Andrew; Gorkowski, Kyle

    2016-09-01

    We deployed Aerodyne Research Inc.’s first Cavity Attenuated Phase Shift extinction (CAPS PMex) monitor (built by Aerodyne) that measures light extinction by using a visible-light-emitting diode (LED) as a light source, a sample cell incorporating two high-reflectivity mirrors centered at the wavelength of the LED, and a vacuum photodiode detector in Cape Cod in 2012/13 for the U.S. Department of Energy (DOE) Atmospheric Radiation Measurement (ARM) Climate Research Facility’s Two-Column Aerosol Project (TCAP). The efficacy of this instrument is based on the fact that aerosols are broadband scatterers and absorbers of light. The input LED is square-wave modulated and passed through the sample cell that distorts it due to exponential decay by aerosol light absorption and scattering; this is measured at the detector. The amount of phase shift of the light at the detector is used to determine the light extinction. This extinction measurement provides an absolute value, requiring no calibration. The goal was to compare the CAPS performance with direct measurements of absorption with ARM’s baseline photoacoustic soot spectrometer (PASS-3) and nephelometer instruments to evaluate its performance.

  6. Extinction spectra of mineral dust aerosol components in an environmental aerosol chamber: IR resonance studies

    NASA Astrophysics Data System (ADS)

    Mogili, Praveen K.; Yang, K. H.; Young, Mark A.; Kleiber, Paul D.; Grassian, Vicki H.

    Mineral dust aerosol plays an important role in determining the physical and chemical equilibrium of the atmosphere. To better understand the impact that mineral dust aerosol may have on climate forcing and on remote sensing, we have initiated a study of the optical properties of important components of mineral dust aerosol including silicate clays (illite, kaolinite, and montmorillonite), quartz, anhydrite, and calcite. The extinction spectra are measured in an environmental simulation chamber over a broad wavelength range, which includes both the IR (650-5000 cm -1) and UV-vis (12,500-40,000 cm -1) spectral regions. In this paper, we focus on the IR region from 800 to 1500 cm -1, where many of these mineral dust constituents have characteristic vibrational resonance features. Experimental spectra are compared with Mie theory simulations based on published mineral optical constants. We find that Mie theory generally does a poor job in fitting the IR resonance peak positions and band profiles for nonspherical aerosols in the accumulation mode size range ( D˜0.1-2.5 μm). We explore particle shape effects on the IR resonance line profiles by considering analytic models for extinction of particles with characteristic shapes (i.e. disks, needles, and ellipsoids). Interestingly, Mie theory often appears to give more accurate results for the absorption line profiles of larger particles that fall in the coarse mode size range.

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

    NASA Technical Reports Server (NTRS)

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

    1978-01-01

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

  8. Applications of broadband cavity enhanced spectroscopy for measurements of trace gases and aerosols

    NASA Astrophysics Data System (ADS)

    Washenfelder, R. A.; Attwood, A. R.; Brock, C. A.; Brown, S. S.; Dube, W. P.; Flores, J. M.; Langford, A. O.; Min, K. E.; Rudich, Y.; Stutz, J.; Wagner, N.; Young, C.; Zarzana, K. J.

    2015-12-01

    Broadband cavity enhanced spectroscopy (BBCES) uses a broadband light source, optical cavity, and multichannel detector to measure light extinction with high sensitivity. This method differs from cavity ringdown spectroscopy, because it uses an inexpensive, incoherent light source and allows optical extinction to be determined simultaneously across a broad wavelength region.Spectral fitting methods can be used to retrieve multiple absorbers across the observed wavelength region. We have successfully used this method to measure glyoxal (CHOCHO), nitrous acid (HONO), and nitrogen dioxide (NO2) from ground-based and aircraft-based sampling platforms. The detection limit (2-sigma) in 5 s for retrievals of CHOCHO, HONO and NO2 is 32, 250 and 80 parts per trillion (pptv).Alternatively, gas-phase absorbers can be chemically removed to allow the accurate determination of aerosol extinction. In the laboratory, we have used the aerosol extinction measurements to determine scattering and absorption as a function of wavelength. We have deployed a ground-based field instrument to measure aerosol extinction, with a detection limit of approximately 0.2 Mm-1 in 1 min.BBCES methods are most widely used in the near-ultraviolet and visible spectral region. Recently, we have demonstrated measurements at 315-350 nm for formaldehyde (CH2O) and NO2. Extending the technique further into the ultraviolet spectral region will allow important additional measurements of trace gas species and aerosol extinction.

  9. Light source effects on aerosol photoacoustic spectroscopy measurements

    NASA Astrophysics Data System (ADS)

    Radney, James G.; Zangmeister, Christopher D.

    2017-01-01

    Photoacoustic spectroscopy measurements of flame-generated soot aerosol coated with small amounts of water yielded absorption enhancements that were dependent on the laser used: quasi-continuous wave (Q-CW, ≈650 ps pulse duration and 78 MHz repetition rate) versus continuous wave (CW). Water coating thickness was controlled by exposing the aerosol to a set relative humidity (RH). At ≈85% RH, the mass of the soot particles increased by an amount comparable to a monolayer of water being deposited and enhanced the measured absorption by 36% and 15% for the Q-CW and CW lasers, respectively. Extinction measurements were also performed using a cavity ring-down spectrometer (extinction equals the sum of absorption and scattering) with a CW laser and negligible enhancement was observed at all RH. These findings demonstrate that source choice can impact measurements of aerosols with volatile coatings and that the absorption enhancements at high RH previously measured by Radney and Zangmeister [1] are the result of laser source used (Q-CW) and not from an increase in the particle absorption cross section.

  10. Optical modeling of aerosol extinction for remote sensing in the marine environment

    NASA Astrophysics Data System (ADS)

    Kaloshin, G. A.

    2013-05-01

    A microphysical model is presented for the surface layer marine and coastal atmospheric aerosols that is based on long-term observations of size distributions for 0.01-100 μm particles in different geographic sites. The fundamental feature of the model is a parameterization of amplitudes and widths for aerosol modes of the aerosol size distribution function (ASDF) as functions of fetch and wind speed. The shape of the ASDF and its dependence on meteorological parameters, altitudes above sea level (H), fetch (X), wind speed (U) and relative humidity (RH) are investigated. The spectral profiles of the aerosol extinction coefficients calculated by MaexPro (Marine Aerosol Extinction Profiles) are in good agreement with observational data and the numerical results obtained from the Navy Aerosol Model (NAM) and the Advanced Navy Aerosol Model (ANAM). Moreover, MaexPro was found to be an accurate and reliable tool for investigation of the optical properties of atmospheric aerosols.

  11. Toward a Combined SAGE II-HALOE Aerosol Climatology: An Evaluation of HALOE Version 19 Stratospheric Aerosol Extinction Coefficient Observations

    NASA Technical Reports Server (NTRS)

    Thomason, L. W.

    2012-01-01

    Herein, the Halogen Occultation Experiment (HALOE) aerosol extinction coefficient data is evaluated in the low aerosol loading period after 1996 as the first necessary step in a process that will eventually allow the production of a combined HALOE/SAGE II (Stratospheric Aerosol and Gas Experiment) aerosol climatology of derived aerosol products including surface area density. Based on these analyses, it is demonstrated that HALOE's 3.46 microns is of good quality above 19 km and suitable for scientific applications above that altitude. However, it is increasingly suspect at lower altitudes and should not be used below 17 km under any circumstances after 1996. The 3.40 microns is biased by about 10% throughout the lower stratosphere due to the failure to clear NO2 but otherwise appears to be a high quality product down to 15 km. The 2.45 and 5.26 micron aerosol extinction coefficient measurements are clearly biased and should not be used for scientific applications after the most intense parts of the Pinatubo period. Many of the issues in the aerosol data appear to be related to either the failure to clear some interfering gas species or doing so poorly. For instance, it is clear that the 3.40micronaerosol extinction coefficient measurements can be improved through the inclusion of an NO2 correction and could, in fact, end up as the highest quality overall HALOE aerosol extinction coefficient measurement. It also appears that the 2.45 and 5.26 micron channels may be improved by updating the Upper Atmosphere Pilot Database which is used as a resource for the removal of gas species otherwise not available from direct HALOE measurements. Finally, a simple model to demonstrate the promise of mixed visible/infrared aerosol extinction coefficient ensembles for the retrieval of bulk aerosol properties demonstrates that a combined HALOE/SAGE II aerosol climatology is feasible and may represent a substantial improvement over independently derived data sets.

  12. Accuracy of near-surface aerosol extinction determined from columnar aerosol optical depth measurements in Reno, NV, USA

    NASA Astrophysics Data System (ADS)

    Loría-Salazar, S. Marcela; Arnott, W. Patrick; Moosmüller, Hans

    2014-10-01

    The aim of the present work is a detailed analysis of aerosol columnar optical depth as a tool to determine near-surface aerosol extinction in Reno, Nevada, USA, during the summer of 2012. Ground and columnar aerosol optical properties were obtained by use of in situ Photoacoustic and Integrated Nephelometer and Cimel CE-318 Sun photometer instruments, respectively. Both techniques showed that seasonal weather changes and fire plumes had enormous influence on local aerosol optics. The apparent optical height followed the shape but not magnitude of the development of the convective boundary layer when fire conditions were not present. Back trajectory analysis demonstrated that a local flow known as the Washoe Zephyr circulation often induced aerosol transport from Northern California over the Sierra Nevada Mountains that increased the aerosol optical depth at 500 nm during afternoons when compared with mornings. Aerosol fine mode fraction indicated that afternoon aerosols in June and July and fire plumes in August were dominated by submicron particles, suggesting upwind urban plume biogenically enhanced evolution toward substantial secondary aerosol formation. This fine particle optical depth was inferred to be beyond the surface, thereby complicating use of remote sensing measurements for near-ground aerosol extinction measurements. It is likely that coarse mode depletes fine mode aerosol near the surface by coagulation and condensation of precursor gases.

  13. Spectrally-resolved measurements of aerosol extinction at ultraviolet and visible wavelengths

    NASA Astrophysics Data System (ADS)

    Flores, M.; Washenfelder, R. A.; Brock, C. A.; Brown, S. S.; Rudich, Y.

    2012-12-01

    Aerosols play an important role in the Earth's radiative budget. Aerosol extinction includes both the scattering and absorption of light, and these vary with wavelength, aerosol diameter, and aerosol composition. Historically, aerosol absorption has been measured using filter-based or extraction methods that are prone to artifacts. There have been few investigations of ambient aerosol optical properties at the blue end of the visible spectrum and into the ultraviolet. Brown carbon is particularly important in this spectral region, because it both absorbs and scatters light, and encompasses a large and variable group of organic compounds from biomass burning and secondary organic aerosol. We have developed a laboratory instrument that combines new, high-power LED light sources with high-finesse optical cavities to achieve sensitive measurements of aerosol optical extinction. This instrument contains two broadband channels, with spectral coverage from 360 - 390 nm and 385 - 420 nm. Using this instrument, we report aerosol extinction in the ultraviolet and near-visible spectral region as a function of chemical composition and structure. We have measured the extinction cross-sections between 360 - 420 nm with 0.5 nm resolution using different sizes and concentrations of polystyrene latex spheres, ammonium sulfate, and Suwannee River fulvic acid. Fitting the real and imaginary part of the refractive index allows the absorption and scattering to be determined.

  14. Raman Lidar Measurements of Aerosol Extinction and Backscattering. Report 1; Methods and Comparisons

    NASA Technical Reports Server (NTRS)

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

    1998-01-01

    This paper examines the aerosol backscattering and extinction profiles measured at night by the NASA Goddard Space Flight Center Scanning Raman Lidar (SRL) during the remote cloud sensing (RCS) intensive operations period (IOP) at the Department of Energy Atmospheric Radiation Measurement (ARM) southern Great Plains (SGP) site in April 1994. These lidar data are used to derive aerosol profiles for altitudes between 0.0 1 5 and 5 km. Since this lidar detects Raman scattering from nitrogen and oxygen molecules as well as the elastic scattering from molecules and aerosols, it measures both aerosol backscattering and extinction simultaneously. The aerosol extinction/backscattering ratio varied between approximately 30 sr and 75 sr at 351 nm. Aerosol optical thicknesses derived by integrating the lidar profiles of aerosol extinction measured at night between 0. I and 5 km are found to be about 10-40% lower than those measured by a Sun photometer during the day. This difference is attributed to the contribution by stratospheric aerosols not included in the lidar estimates as well as to diurnal differences in aerosol properties and concentrations. Aerosol profiles close to the surface were acquired by pointing the lidar nearly horizontally. Measurements of aerosol scattering from a tower-mounted nephelometer are found to be 40% lower than lidar measurements of aerosol extinction over a wide range of relative humidities even after accounting for the difference in wavelengths. The reasons for this difference are not clear but may be due to the inability of the nephelometer to accurately measure scattering by large particles.

  15. Light extinction by Secondary Organic Aerosol: an intercomparison of three broadband cavity spectrometers

    NASA Astrophysics Data System (ADS)

    Varma, R. M.; Ball, S. M.; Brauers, T.; Dorn, H.-P.; Heitmann, U.; Jones, R. L.; Platt, U.; Pöhler, D.; Ruth, A. A.; Shillings, A. J. L.; Thieser, J.; Wahner, A.; Venables, D. S.

    2013-07-01

    Broadband optical cavity spectrometers are maturing as a technology for trace gas detection, but only recently have they been used to retrieve the extinction coefficient of aerosols. Sensitive broadband extinction measurements allow explicit separation of gas and particle phase spectral contributions, as well as continuous spectral measurements of aerosol extinction in favourable cases. In this work, we report an intercomparison study of the aerosol extinction coefficients measured by three such instruments: a broadband cavity ring-down spectrometer (BBCRDS), a cavity-enhanced differential optical absorption spectrometer (CE-DOAS), and an incoherent broadband cavity-enhanced absorption spectrometer (IBBCEAS). Experiments were carried out in the SAPHIR atmospheric simulation chamber as part of the NO3Comp campaign to compare the measurement capabilities of NO3 and N2O5 instrumentation. Aerosol extinction coefficients between 655 and 690 nm are reported for secondary organic aerosols (SOA) formed by the NO3 oxidation of β-pinene under dry and humid conditions. Despite different measurement approaches and spectral analysis procedures, the three instruments retrieved aerosol extinction coefficients that were in close agreement. The refractive index of SOA formed from the β-pinene + NO3 reaction was 1.61, and was not measurably affected by the chamber humidity or by aging of the aerosol over several hours. This refractive index is significantly larger than SOA refractive indices observed in other studies of OH and ozone-initiated terpene oxidations, and may be caused by the large proportion of organic nitrates in the particle phase. In an experiment involving ammonium sulphate particles the aerosol extinction coefficients as measured by IBBCEAS were found to be in reasonable agreement with those calculated using Mie theory. The results of the study demonstrate the potential of broadband cavity spectrometers for determining the optical properties of aerosols.

  16. Light extinction by secondary organic aerosol: an intercomparison of three broadband cavity spectrometers

    NASA Astrophysics Data System (ADS)

    Varma, R. M.; Ball, S. M.; Brauers, T.; Dorn, H.-P.; Heitmann, U.; Jones, R. L.; Platt, U.; Pöhler, D.; Ruth, A. A.; Shillings, A. J. L.; Thieser, J.; Wahner, A.; Venables, D. S.

    2013-11-01

    Broadband optical cavity spectrometers are maturing as a technology for trace-gas detection, but only recently have they been used to retrieve the extinction coefficient of aerosols. Sensitive broadband extinction measurements allow explicit separation of gas and particle phase spectral contributions, as well as continuous spectral measurements of aerosol extinction in favourable cases. In this work, we report an intercomparison study of the aerosol extinction coefficients measured by three such instruments: a broadband cavity ring-down spectrometer (BBCRDS), a cavity-enhanced differential optical absorption spectrometer (CE-DOAS), and an incoherent broadband cavity-enhanced absorption spectrometer (IBBCEAS). Experiments were carried out in the SAPHIR atmospheric simulation chamber as part of the NO3Comp campaign to compare the measurement capabilities of NO3 and N2O5 instrumentation. Aerosol extinction coefficients between 655 and 690 nm are reported for secondary organic aerosols (SOA) formed by the NO3 oxidation of β-pinene under dry and humid conditions. Despite different measurement approaches and spectral analysis procedures, the three instruments retrieved aerosol extinction coefficients that were in close agreement. The refractive index of SOA formed from the β-pinene + NO3 reaction was 1.61, and was not measurably affected by the chamber humidity or by aging of the aerosol over several hours. This refractive index is significantly larger than SOA refractive indices observed in other studies of OH and ozone-initiated terpene oxidations, and may be caused by the large proportion of organic nitrates in the particle phase. In an experiment involving ammonium sulfate particles, the aerosol extinction coefficients as measured by IBBCEAS were found to be in reasonable agreement with those calculated using the Mie theory. The results of the study demonstrate the potential of broadband cavity spectrometers for determining the optical properties of aerosols.

  17. Spectral Aerosol Extinction (SpEx): a new instrument for in situ ambient aerosol extinction measurements across the UV/visible wavelength range

    NASA Astrophysics Data System (ADS)

    Jordan, C. E.; Anderson, B. E.; Beyersdorf, A. J.; Corr, C. A.; Dibb, J. E.; Greenslade, M. E.; Martin, R. F.; Moore, R. H.; Scheuer, E.; Shook, M. A.; Thornhill, K. L.; Troop, D.; Winstead, E. L.; Ziemba, L. D.

    2015-06-01

    We introduce a new instrument for the measurement of in situ ambient aerosol extinction over the 300-700 nm wavelength range, the Spectral Aerosol Extinction (SpEx) instrument. This measurement capability is envisioned to complement existing in situ instrumentation, allowing for simultaneous measurement of the evolution of aerosol optical, chemical, and physical characteristics in the ambient environment. In this work, a detailed description of the instrument is provided along with characterization tests performed in the laboratory. Measured spectra of NO2 and polystyrene latex spheres (PSLs) agreed well with theoretical calculations. Good agreement was also found with simultaneous aerosol extinction measurements at 450, 530, and 630 nm using CAPS PMex instruments in a series of 22 tests including non-absorbing compounds, dusts, soot, and black and brown carbon analogs. SpEx can more accurately distinguish the presence of brown carbon from other absorbing aerosol due to its 300 nm lower wavelength limit compared to measurements limited to visible wavelengths. Extinction spectra obtained with SpEx contain more information than can be conveyed by a simple power law fit (typically represented by Ångström Exponents). Planned future improvements aim to lower detection limits and ruggedize the instrument for mobile operation.

  18. Comparison of LIDAR and Cavity Ring-Down Measurements of Aerosol Extinction and Study of Inferred Aerosol Gradients

    NASA Astrophysics Data System (ADS)

    Eberhard, W. L.; Massoli, P.; McCarty, B. J.; Machol, J. L.; Tucker, S. C.

    2007-12-01

    A LIDAR and a Cavity Ring-Down Aerosol Extinction Spectrometer (CRD) instrument simultaneously measured aerosol extinction at 355-nm wavelength from aboard the Research Vessel Ronald H. Brown during the Texas Air Quality Study II campaign. The CRD measured air sampled from the top of the common mast used by several in situ aerosol optical and chemical instruments. The LIDAR's scan sequence included near-horizontal stares (2° elevation angle) with pointing corrected for ship's roll. Aerosol extinction was retrieved using a variant of the slope method. The LIDAR therefore sampled air over a short vertical extent with midpoint higher above the surface than the CRD intake and at a horizontal distance of as much as a few kilometers. The CRD measured aerosol extinction at dry and at high (near-ambient) relative humidity (RH) levels, which were used to scale the measurements to ambient RH for the comparisons. Data from the two instruments for well-mixed conditions (supported by turbulence and atmospheric stability data) are compared to evaluate the degree of agreement between the two methods and reasons for differences. For instances of larger differences, the aerosol gradient below approximately 100 m altitude is inferred and examined in context of low-level meteorological parameters and LIDAR measurements at higher angles.

  19. Seasonal and diurnal variations of aerosol extinction profile and type distribution from CALIPSO 5-year observations

    NASA Astrophysics Data System (ADS)

    Huang, Lei; Jiang, Jonathan H.; Tackett, Jason L.; Su, Hui; Fu, Rong

    2013-05-01

    The new Level 3 aerosol profile data derived from the Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observations (CALIPSO) provide a multiyear global aerosol distribution with high vertical resolution. We analyzed seasonal and diurnal variations of the vertical distributions of aerosol properties represented by 5-year CALIPSO data. Results show that dust, smoke, and polluted dust are the most frequently detected aerosol types during all seasons. Dust is the dominant type, especially in the middle to upper troposphere, over most areas during boreal spring and summer, while smoke and polluted dust tend to dominate during biomass burning seasons. The seasonal variations of dust layer top height and dust contribution to all-aerosol extinction are positively correlated with the seasonal variation of the dust occurrence frequency. The seasonal cycle of aerosol properties over west Australia is similar to that over biomass burning regime areas, despite its desert regime. In general, smoke is detected more frequently from the lower to middle troposphere; clean marine and polluted continental aerosols are detected more frequently, while polluted dust is detected less frequently, in the lower troposphere during nighttime than daytime. The all-aerosol extinction is generally larger, and the aerosol layer top is detected at high altitudes more frequently during nighttime than daytime. The diurnal changes of aerosol properties are similar within the same aerosol regime. Dust extinction shows little diurnal variation except when dust is the dominant aerosol type. The results contribute to an initial global 3-D aerosol climatology which will likely be extended and improved in the future.

  20. Spectral aerosol extinction (SpEx): a new instrument for in situ ambient aerosol extinction measurements across the UV/visible wavelength range

    NASA Astrophysics Data System (ADS)

    Jordan, C. E.; Anderson, B. E.; Beyersdorf, A. J.; Corr, C. A.; Dibb, J. E.; Greenslade, M. E.; Martin, R. F.; Moore, R. H.; Scheuer, E.; Shook, M. A.; Thornhill, K. L.; Troop, D.; Winstead, E. L.; Ziemba, L. D.

    2015-11-01

    We introduce a new instrument for the measurement of in situ ambient aerosol extinction over the 300-700 nm wavelength range, the spectral aerosol extinction (SpEx) instrument. This measurement capability is envisioned to complement existing in situ instrumentation, allowing for simultaneous measurement of the evolution of aerosol optical, chemical, and physical characteristics in the ambient environment. In this work, a detailed description of the instrument is provided along with characterization tests performed in the laboratory. Measured spectra of NO2 and polystyrene latex spheres (PSLs) agreed well with theoretical calculations. Good agreement was also found with simultaneous aerosol extinction measurements at 450, 530, and 630 nm using CAPS PMex instruments in a series of 22 tests including nonabsorbing compounds, dusts, soot, and black and brown carbon analogs. SpEx measurements are expected to help identify the presence of ambient brown carbon due to its 300 nm lower wavelength limit compared to measurements limited to longer UV and visible wavelengths. Extinction spectra obtained with SpEx contain more information than can be conveyed by a simple power law fit (typically represented by Ångström exponents). Planned future improvements aim to lower detection limits and ruggedize the instrument for mobile operation.

  1. Visible and infrared extinction of atmospheric aerosol in the marine and coastal environment.

    PubMed

    Kaloshin, Gennady A

    2011-05-10

    The microphysical model Marine Aerosol Extinction Profiles (MaexPro) for surface layer marine and coastal atmospheric aerosols, which is based on long-term observations of size distributions for 0.01-100 μm particles, is presented. The fundamental feature of the model is a parameterization of amplitudes and widths for aerosol modes of the aerosol size distribution function (ASDF) as functions of fetch and wind speed. The shape of the ASDF and its dependence on meteorological parameters, altitudes above the sea level (H), fetch (X), wind speed (U), and relative humidity is investigated. The model is primarily to characterize aerosols for the near-surface layer (within 25 m). The model is also applicable to higher altitudes within the atmospheric boundary layer, where the change in the vertical profile of aerosol is not very large. In this case, it is only valid for "clean" marine environments, in the absence of air pollution or any other major sources of continental aerosols, such desert dust or smoke from biomass burning. The spectral profiles of the aerosol extinction coefficients calculated by MaexPro are in good agreement with observational data and the numerical results obtained by the well-known Navy Aerosol Model and Advanced Navy Aerosol Model codes. Moreover, MaexPro was found to be an accurate and reliable instrument for investigation of the optical properties of atmospheric aerosols.

  2. Spectral Aerosol Extinction (SpEx): A New Instrument for In situ Ambient Aerosol Extinction Measurements Across the UV/Visible Wavelength Range

    NASA Technical Reports Server (NTRS)

    Jordan, C. E.; Anderson, B. E.; Beyersdorf, A. J.; Corr, C. A.; Dibb, J. E.; Greenslade, M. E.; Martin, R. F.; Moore, R. H.; Scheuer, E.; Shook, M. A.; Thornhill, K. L.; Troop, D.; Winstead, Edward L.; Ziemba, L. D.

    2015-01-01

    We introduce a new instrument for the measurement of in situ ambient aerosol extinction over the 300-700 nm wavelength range, the Spectral Aerosol Extinction (SpEx) instrument. This measurement capability is envisioned to complement existing in situ instrumentation, allowing for simultaneous measurement of the evolution of aerosol optical, chemical, and physical characteristics in the ambient environment. In this work, a detailed description of the instrument is provided along with characterization tests performed in the laboratory. Measured spectra of NO2 and polystyrene latex spheres agreed well with theoretical calculations. Good agreement was also found with simultaneous aerosol extinction measurements at 450, 530, and 630 nm using CAPS PMex instruments in a series of 22 tests including non-absorbing compounds, dusts, soot, and black and brown carbon analogs. SpEx can more accurately distinguish the presence of brown carbon from other absorbing aerosol due to its 300 nm lower wavelength limit compared to measurements limited to visible wavelengths. In addition, the spectra obtained by SpEx carry more information than can be conveyed by a simple power law fit that is typically defined by the use of Angstrom Exponents. Future improvements aim at lowering detection limits and ruggedizing the instrument for mobile operation.

  3. In Situ Aerosol Profile Measurements and Comparisons with SAGE 3 Aerosol Extinction and Surface Area Profiles at 68 deg North

    NASA Technical Reports Server (NTRS)

    2005-01-01

    Under funding from this proposal three in situ profile measurements of stratospheric sulfate aerosol and ozone were completed from balloon-borne platforms. The measured quantities are aerosol size resolved number concentration and ozone. The one derived product is aerosol size distribution, from which aerosol moments, such as surface area, volume, and extinction can be calculated for comparison with SAGE III measurements and SAGE III derived products, such as surface area. The analysis of these profiles and comparison with SAGE III extinction measurements and SAGE III derived surface areas are provided in Yongxiao (2005), which comprised the research thesis component of Mr. Jian Yongxiao's M.S. degree in Atmospheric Science at the University of Wyoming. In addition analysis continues on using principal component analysis (PCA) to derive aerosol surface area from the 9 wavelength extinction measurements available from SAGE III. Ths paper will present PCA components to calculate surface area from SAGE III measurements and compare these derived surface areas with those available directly from in situ size distribution measurements, as well as surface areas which would be derived from PCA and Thomason's algorithm applied to the four wavelength SAGE II extinction measurements.

  4. Using Airborne High Spectral Resolution Lidar Data to Evaluate Combined Active Plus Passive Retrievals of Aerosol Extinction Profiles

    NASA Technical Reports Server (NTRS)

    Burton, S. P.; Ferrare, R. A.; Kittaka, C.; Hostetler, C. A.; Hair, J. W.; Obland, M. D.; Rogers, R. R.; Cook, A. L.; Haper, D. B.

    2008-01-01

    Aerosol extinction profiles are derived from backscatter data by constraining the retrieval with column aerosol optical thickness (AOT), for example from coincident MODIS observations and without reliance on a priori assumptions about aerosol type or optical properties. The backscatter data were acquired with the NASA Langley High Spectral Resolution Lidar (HSRL). The HSRL also simultaneously measures extinction independently, thereby providing an ideal data set for evaluating the constrained retrieval of extinction from backscatter. We will show constrained extinction retrievals using various sources of column AOT, and examine comparisons with the HSRL extinction measurements and with a similar retrieval using data from the CALIOP lidar on the CALIPSO satellite.

  5. Comparison of SAGE II and lidar stratospheric aerosol extinction datasets after the Mt Pinatubo eruption

    NASA Astrophysics Data System (ADS)

    Antuna Marrero, Juan Carlos

    Both observations and modeling demonstrate that stratospheric aerosols from intense explosive volcanic eruptions cause several different effects on weather and climate. The main effect is the cooling of the earth's surface between one and three years after the eruption. Stratospheric heating, winter warming on the Northern Hemisphere continental areas, ozone depletion and cirrus cloud seeding are several other effects attributed to stratospheric aerosols. Studying the stratospheric aerosol features and their effects on weather and climate requires a precise knowledge of their physical and optical properties. Accurate volcanic climate effects simulations using state of the art general circulation models require detailed and precise information about stratospheric aerosol concentration, distribution in space and time, and optical properties. Satellite aerosol extinction measurements are the main source of information for such studies, however they have gaps because of missing data and time and space coverage. Although lidar aerosol backscattering measurements have been recognized for a long time as a valuable complementary source to the satellite information, they have not been used so far for such a goal. A necessary step for combining both sources of information is the comparison between them, but only very few and limited ones have been conducted. I conducted the most comprehensive comparison ever between lidar and SAGE II aerosol extinction, covering the two and half years after the 1991 Mount Pinatubo eruption. I address the crucial issue of the aerosol extinction variability at the daily scale and I calculated its quantitative magnitudes for the first time. Using both SAGE II coincident sunrise-sunset measurements and lidar measurements one and two days apart I determine it ranges between 50 and 150%. I compared extinction-derived profiles from five lidars with space and time coincident SAGE II extinction measurements. Three lidars are in the tropics and two in

  6. The CU Airborne MAX-DOAS instrument: vertical profiling of aerosol extinction and trace gases

    NASA Astrophysics Data System (ADS)

    Baidar, S.; Oetjen, H.; Coburn, S.; Dix, B.; Ortega, I.; Sinreich, R.; Volkamer, R.

    2013-03-01

    The University of Colorado Airborne Multi-Axis Differential Optical Absorption Spectroscopy (CU AMAX-DOAS) instrument uses solar stray light to detect and quantify multiple trace gases, including nitrogen dioxide (NO2), glyoxal (CHOCHO), formaldehyde (HCHO), water vapor (H2O), nitrous acid (HONO), iodine monoxide (IO), bromine monoxide (BrO), and oxygen dimers (O4) at multiple wavelengths (absorption bands at 360, 477, 577, 632 nm) simultaneously in the open atmosphere. The instrument is unique as it (1) features a motion compensation system that decouples the telescope field of view from aircraft movements in real time (<0.35° accuracy), and (2) includes measurements of solar stray light photons from nadir, zenith, and multiple elevation angles forward and below the plane by the same spectrometer/detector system. Sets of solar stray light spectra collected from nadir to zenith scans provide some vertical profile information within 2 km above and below the aircraft altitude, and the vertical column density (VCD) below the aircraft is measured in nadir view. Maximum information about vertical profiles is derived simultaneously for trace gas concentrations and aerosol extinction coefficients over similar spatial scales and with a vertical resolution of typically 250 m during aircraft ascent/descent. The instrument is described, and data from flights over California during the CalNex (California Research at the Nexus of Air Quality and Climate Change) and CARES (Carbonaceous Aerosols and Radiative Effects Study) air quality field campaigns is presented. Horizontal distributions of NO2 VCD (below the aircraft) maps are sampled with typically 1 km resolution, and show good agreement with two ground-based MAX-DOAS instruments (slope = 0.95 ± 0.09, R2 = 0.86). As a case study vertical profiles of NO2, CHOCHO, HCHO, and H2O concentrations and aerosol extinction coefficients, ɛ, at 477 nm calculated from O4 measurements from a low approach at Brackett airfield inside the

  7. SAGE 1 and SAM 2 measurements of 1 micron aerosol extinction in the free troposphere

    NASA Technical Reports Server (NTRS)

    Kent, G. S.; Farrukh, U. O.; Wang, P. H.; Deepak, A.

    1988-01-01

    The SAGE 1 and SAM 2 satellite sensors were designed to measure, with global coverage, the 1 micron extinction produced by the stratospheric aerosol. In the absence of high altitude cloud, similar measurements may be made for the free tropospheric aerosol. Median extinction values in the Northern Hemisphere, for altitudes between 5 and 10 km, are found to be one-half to one order of magnitude greater than values at corresponding latitudes in the Southern Hemisphere. In addition, a seasonal increase by a factor of 1.5 yields 2 is observed in both hemispheres in local spring and summer. Following major volcanic eruptions, a long-lived enhancement of the aerosol extinction is observed for altitudes above 5 km.

  8. SAGE I and SAM II measurements of 1 micron aerosol extinction in the free troposphere

    NASA Technical Reports Server (NTRS)

    Kent, G. S.; Farrukh, U. O.; Wang, P. H.; Deepak, A.

    1988-01-01

    The SAGE-I and SAM-II satellite sensors were designed to measure, with global coverage, the 1 micron extinction produced by the stratospheric aerosol. In the absence of high altitude clouds, similar measurements may be made for the free tropospheric aerosol. Median extinction values at middle and high latitudes in the Northern Hemisphere, for altitudes between 5 and 10 km, are found to be one-half to one order of magnitude greater than values at corresponding latitudes in the Southern Hemisphere. In addition, a seasonal increase by a factor of 1.5-2 was observed in both hemispheres, in 1979-80, in local spring and summer. Following major volcanic eruptions, a long-lived enhancement of the aerosol extinction is observed for altitudes above 5 km.

  9. Enhanced extinction of visible radiation due to hydrated aerosols in mist and fog

    NASA Astrophysics Data System (ADS)

    Elias, T.; Dupont, J.-C.; Hammer, E.; Hoyle, C. R.; Haeffelin, M.; Burnet, F.; Jolivet, D.

    2015-06-01

    The study assesses the contribution of aerosols to the extinction of visible radiation in the mist-fog-mist cycle. Relative humidity is large in the mist-fog-mist cycle, and aerosols most efficient in interacting with visible radiation are hydrated and compose the accumulation mode. Measurements of the microphysical and optical properties of these hydrated aerosols with diameters larger than 0.4 μm were carried out near Paris, during November 2011, under ambient conditions. Eleven mist-fog-mist cycles were observed, with a cumulated fog duration of 96 h, and a cumulated mist-fog-mist cycle duration of 240 h. In mist, aerosols grew by taking up water at relative humidities larger than 93%, causing a visibility decrease below 5 km. While visibility decreased down from 5 to a few kilometres, the mean size of the hydrated aerosols increased, and their number concentration (Nha) increased from approximately 160 to approximately 600 cm-3. When fog formed, droplets became the strongest contributors to visible radiation extinction, and liquid water content (LWC) increased beyond 7 mg m-3. Hydrated aerosols of the accumulation mode co-existed with droplets, as interstitial non-activated aerosols. Their size continued to increase, and some aerosols achieved diameters larger than 2.5 μm. The mean transition diameter between the aerosol accumulation mode and the small droplet mode was 4.0 ± 1.1 μm. Nha also increased on average by 60 % after fog formation. Consequently, the mean contribution to extinction in fog was 20 ± 15% from hydrated aerosols smaller than 2.5 μm and 6 ± 7% from larger aerosols. The standard deviation was large because of the large variability of Nha in fog, which could be smaller than in mist or 3 times larger. The particle extinction coefficient in fog can be computed as the sum of a droplet component and an aerosol component, which can be approximated by 3.5 Nha (Nha in cm-3 and particle extinction coefficient in Mm-1. We observed an influence of

  10. Measurements of Stratospheric Pinatubo Aerosol Extinction Profiles by a Raman Lidar

    NASA Technical Reports Server (NTRS)

    Abo, Makoto; Nagasawa, Chikao

    1992-01-01

    The Raman lidar has been used for remote measurements of water vapor, ozone and atmospheric temperature in the lower troposphere because the Raman cross section is three orders smaller than the Rayleigh cross section. We estimated the extinction coefficients of the Pinatubo volcanic aerosol in the stratosphere using a Raman lidar. If the precise aerosol extinction coefficients are derived, the backscatter coefficient of a Mie scattering lidar will be more accurately estimated. The Raman lidar has performed to measure density profiles of some species using Raman scattering. Here we used a frequency-doubled Nd:YAG laser for transmitter and received nitrogen vibrational Q-branch Raman scattering signal. Ansmann et al. (1990) derived tropospherical aerosol extinction profiles with a Raman lidar. We think that this method can apply to dense stratospheric aerosols such as Pinatubo volcanic aerosols. As dense aerosols are now accumulated in the stratosphere by Pinatubo volcanic eruption, the error of Ramen lidar signal regarding the fluctuation of air density can be ignored.

  11. In situ measurement of the infrared absorption and extinction of chemical and biologically derived aerosols using flow-through photoacoustics

    NASA Astrophysics Data System (ADS)

    Gurton, Kristan P.; Dahmani, Rachid; Ligon, David; Bronk, Burt V.

    2005-07-01

    In an effort to establish a more reliable set of optical cross sections for a variety of chemical and biological aerosol simulants, we have developed a flow-through photoacoustic system that is capable of measuring absolute, mass-normalized extinction and absorption cross sections. By employing a flow-through design we avoid issues associated with closed aerosol photoacoustic systems and improve sensitivity. Although the results shown here were obtained for the tunable CO2 laser waveband region, i.e., 9.20-10.80 μm, application to other wavelengths is easily achievable. The aerosols considered are categorized as biological, chemical, and inorganic in origin, i.e., Bacillus atrophaeus endospores, dimethicone silicone oil (SF-96 grade 50), and kaolin clay powder (alumina and silicate), respectively. Results compare well with spectral extinction measured previously by Fourier-transform infrared spectroscopy. Comparisons with Mie theory calculations based on previously published complex indices of refraction and measured size distributions are also presented.

  12. Enhanced extinction of visible radiation due to hydrated aerosols in mist and fog

    NASA Astrophysics Data System (ADS)

    Elias, T.; Dupont, J.-C.; Hammer, E.; Hoyle, C. R.; Haeffelin, M.; Burnet, F.; Jolivet, D.

    2015-01-01

    The study assesses the contribution of aerosols to the extinction of visible radiation in the mist-fog-mist cycle. Measurements of the microphysical and optical properties of hydrated aerosols with diameters larger than 400 nm, composing the accumulation mode, which are the most efficient to interact with visible radiation, were carried out near Paris, during November 2011, in ambient conditions. Eleven mist-fog-mist cycles were observed, with cumulated fog duration of 95 h, and cumulated mist-fog-mist duration of 240 h. In mist, aerosols grew up by taking up water at relative humidities larger than 93%, causing a visibility decrease below 5 km. While visibility decreased down to few km, the mean size of the hydrated aerosols increased, and their number concentration (Nha) increased from approximately 160 to approximately 600 cm-3. When fog formed, droplets became the strongest contributors to visible radiation extinction, and liquid water content (LWC) increased beyond 7 mg m-3. Hydrated aerosols of the accumulation mode co-existed with droplets, as interstitial non-activated aerosols. Their size continued to increase, and a significant proportion of aerosols achieved diameters larger than 2.5 μm. The mean transition diameter between the accumulation mode and the small droplet mode was 4.0 ± 1.1 μm. Moreover Nha increased on average by 60% after fog formation. Consequently the mean aerosol contribution to extinction in fog was 20 ± 15% for diameter smaller than 2.5 μm and 6 ± 7% beyond. The standard deviation is large because of the large variability of Nha in fog, which could be smaller than in mist or three times larger. The particle extinction coefficient in fog can be computed as the sum of a droplet component and an aerosol component, which can be approximated by 3.5 Nha (Nha in cm-3 and particle extinction coefficient in Mm-1). We observed an influence of the main formation process on Nha, but not on the contribution to fog extinction by aerosols

  13. Retrieval of Aerosol Profiles using Multi-Axis Differential Optical Absorption Spectroscopy (MAX-DOAS)

    NASA Astrophysics Data System (ADS)

    Yilmaz, Selami; Frieß, Udo; Apituley, Arnoud; Henzing, Bas; Baars, Holger; Heese, Birgit; Althausen, Dietrich; Adam, Mariana; Putaud, Jean-Philippe; Zieger, Paul; Platt, Ulrich

    2010-05-01

    Multi Axis Differential Absorption Spectroscopy (MAX-DOAS) is a well established measurement technique to derive atmospheric trace gas profiles. Using MAX-DOAS measurements of trace gases with a known vertical profile, like the oxygen-dimer O4, it is possible to retrieve information on atmospheric aerosols. Based on the optimal estimation method, we have developed an algorithm which fits simultaneously measured O4 optical densities and relative intensities at several wavelengths and elevation angles to values simulated by a radiative transfer model. Retrieval parameters are aerosol extinction profile and optical properties such as single scattering albedo, phase function and Angström exponent. In 2008 and 2009 several intercomparison campaigns with established aerosol measurement techniques took place in Cabauw/Netherlands, Melpitz/Germany, Ispra/Italy and Leipzig/Germany, where simultaneous DOAS, lidar, Sun photometer and Nephelometer measurements were performed. Here we present results of the intercomparisons for cloud free conditions. The correlation of the aerosol optical thickness retrieved by the DOAS technique and the Sun photometer shows coefficients of determination from 0.96 to 0.98 and slopes from 0.94 to 1.07. The vertical structure of the DOAS retrieved aerosol extinction profiles compare favourably with the structures seen by the backscatter lidar. However, the vertical spatial development of the boundary layer is reproduced with a lower resolution by the DOAS technique. Strategies for the near real-time retrieval of trace gas profiles, aerosol profiles and optical properties will be discussed as well.

  14. A Laboratory Investigation of Aerosol and Extinction Characteristics for SALTY DOG, NWC 29 and NWC 78 Pyrotechnics

    DTIC Science & Technology

    1980-10-01

    Dispersion Extinction Pyrotechnics Salty Dog Smokes Deliquescent Growth i *0. ABSTRACT (Continue on reverse aide Iti nee.,ary and idently by block... deliquescent aerosol. Results from the laboratory investigation of individual particle growth indicate that the aerosol generated by NVC 78 has the...due to liquid water (i.e., the deliquesced aerosol) absorption at those IR wavelengths. To compare the extinction effectiveness of Salty Dog to that of

  15. Light extinction by aerosols during summer air pollution

    NASA Technical Reports Server (NTRS)

    Kaufman, Y. J.; Fraser, R. S.

    1983-01-01

    In order to utilize satellite measurements of optical thickness over land for estimating aerosol properties during air pollution episodes, the optical thickness was measured from the surface and investigated. Aerosol optical thicknesses have been derived from solar transmission measurements in eight spectral bands within the band lambda 440-870 nm during the summers of 1980 and 1981 near Washington, DC. The optical thicknesses for the eight bands are strongly correlated. It was found that first eigenvalue of the covariance matrix of all observations accounts for 99 percent of the trace of the matrix. Since the measured aerosol optical thickness was closely proportional to the wavelength raised to a power, the aerosol size distribution derived from it is proportional to the diameter (d) raised to a power for the range of diameters between 0.1 to 1.0 micron. This power is insensitive to the total optical thickness. Changes in the aerosol optical thickness depend on several aerosol parameters, but it is difficult to identify the dominant one. The effects of relative humidity and accumulation mode concentration on the optical thickness are analyzed theoretically, and compared with the measurements.

  16. Inter-Comparison of ILAS-II Version 1.4 Aerosol Extinction Coefficient at 780 nm with SAGE II, SAGE III, and POAM III Aerosol Data

    NASA Technical Reports Server (NTRS)

    Saitoh, Naoko; Hayashida, S.; Sugita, T.; Nakajima, H.; Yokota, T.; Hayashi, M.; Shiraishi, K.; Kanzawa, H.; Ejiri, M. K.; Irie, H.; Tanaka, T.; Terao, Y.; Kobayashi, H.; Sasano, Y.; Bevilacqua, R.; Randall, C.; Thomason, L.; Taha, G.

    2006-01-01

    The Improved Limb Atmospheric Spectrometer (ILAS) II on board the Advanced Earth Observing Satellite (ADEOS) II observed stratospheric aerosol in visible/near-infrared/infrared spectra over high latitudes in the Northern and Southern Hemispheres. Observations were taken intermittently from January to March, and continuously from April through October, 2003. We assessed the data quality of ILAS-II version 1.4 aerosol extinction coefficients at 780 nm from comparisons with the Stratospheric Aerosol and Gas Experiment (SAGE) II, SAGE III, and the Polar Ozone and Aerosol Measurement (POAM) III aerosol data. At heights below 20 km in the Northern Hemisphere, aerosol extinction coefficients from ILAS-II agreed with those from SAGE II and SAGE III within 10%, and with those from POAM III within 15%. From 20 to 26 km, ILAS-II aerosol extinction coefficients were smaller than extinction coefficients from the other sensors; differences between ILAS-II and SAGE II ranged from 10% at 20 km to 34% at 26 km. ILAS-II aerosol extinction coefficients from 20 to 25 km in February over the Southern Hemisphere had a negative bias (12-66%) relative to SAGE II aerosol data. The bias increased with increasing altitude. Comparisons between ILAS-II and POAM III aerosol extinction coefficients from January to May in the Southern Hemisphere (defined as the non-Polar Stratospheric Cloud (PSC) season ) yielded qualitatively similar results. From June to October (defined as the PSC season ), aerosol extinction coefficients from ILAS-II were smaller than those from POAM III above 17 km, as in the case of the non-PSC season; however, ILAS-II and POAM III aerosol data were within 15% of each other from 12 to 17 km.

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

    NASA Technical Reports Server (NTRS)

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

    2006-01-01

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

  18. Radiative properties of the background aerosol: absorption component of extinction.

    PubMed

    Clarke, A D; Charlson, R J

    1985-07-19

    The light-scattering and light-absorption coefficients of the global background aerosol define its single-scatter albedo. Continuous, simultaneous measurements of these optical coefficients were made on a daily basis for the remote marine mid-troposphere; such measurements are essential for assessment of the effects of aerosol on atmospheric radiative transfer. Measurements of light-absorption coefficients made at the Mauna Loa Observatory in Hawaii were higher than expected, and the single-scatter albedo was lower than the value often used in radiative transfer models. Soot appears to be the most likely primary absorber, and hemispheric dispersal of this combustion-derived material is suggested.

  19. Daytime aerosol extinction profiles from the combination of CALIOP profiles and AERONET products

    NASA Astrophysics Data System (ADS)

    Marcos, C.; Pedrós, R.; Gómez-Amo, J. L.; Sicard, M.; Utrillas, M. P.; Muñoz, C.; Comerón, A.; Martinez-Lozano, J. A.

    2013-04-01

    The solar background illumination has a strong effect on CALIOP (Cloud-Aerosol Lidar with Orthogonal Polarization) measurements, leading to a decrease in the signal-to-noise ratio of the lidar signal. Because of this, CALIOP level 2 data algorithms might be limited in the retrieval of the properties of the aerosols in the atmosphere. In this work, we present a methodology that combines CALIOP level 1 data with AERONET (Aerosol RObotic NETwork) measurements to retrieve aerosol extinction profiles and lidar ratios in daytime conditions. In this way, we fulfill a two-fold objective: first, we obtain more accurate daytime aerosol information; second, we supplement column integrated measurements from AERONET sun photometers with information about the vertical distribution of aerosols. The methodology has been applied to Burjassot (39.30° N, 0.25° W) and Barcelona (41.39° N, 2.11° E) AERONET stations in the Mediterranean coast of Spain in the period from June 2006 to September 2011. We have found good agreement for the extinction profiles in several study cases of ground lidar measurements in Barcelona, coincident with CALIOP overpasses. Finally, the methodology has proved to be useful for the study of special episodes such as Saharan dust outbreaks.

  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. Using high time resolution aerosol and number size distribution measurements to estimate atmospheric extinction.

    PubMed

    Malm, William C; McMeeking, Gavin R; Kreidenweis, Sonia M; Levin, Ezra; Carrico, Christian M; Day, Derek E; Collett, Jeffrey L; Lee, Taehyoung; Sullivan, Amy P; Raja, Suresh

    2009-09-01

    Rocky Mountain National Park is experiencing reduced visibility and changes in ecosystem function due to increasing levels of oxidized and reduced nitrogen. The Rocky Mountain Atmospheric Nitrogen and Sulfur (RoMANS) study was initiated to better understand the origins of sulfur and nitrogen species as well as the complex chemistry occurring during transport from source to receptor. As part of the study, a monitoring program was initiated for two 1-month time periods--one during the spring and the other during late summer/fall. The monitoring program included intensive high time resolution concentration measurements of aerosol number size distribution, inorganic anions, and cations, and 24-hr time resolution of PM2.5 and PM10 mass, sulfate, nitrate, carbon, and soil-related elements concentrations. These data are combined to estimate high time resolution concentrations of PM2.5 and PM10 aerosol mass and fine mass species estimates of ammoniated sulfate, nitrate, and organic and elemental carbon. Hour-by-hour extinction budgets are calculated by using these species concentration estimates and measurements of size distribution and assuming internal and external particle mixtures. Summer extinction was on average about 3 times higher than spring extinction. During spring months, sulfates, nitrates, carbon mass, and PM10 - PM2.5 mass contributed approximately equal amounts of extinction, whereas during the summer months, carbonaceous material extinction was 2-3 times higher than other species.

  2. Measurement of wavelength-dependent extinction to distinguish between absorbing and nonabsorbing aerosol particulates

    NASA Technical Reports Server (NTRS)

    Portscht, R.

    1977-01-01

    Measurements of spectral transmission factors in smoky optical transmission paths reveal a difference between wavelength exponents of the extinction cross section of high absorption capacity and those of low absorption capacity. A theoretical explanation of this behavior is presented. In certain cases, it is possible to obtain data on the absorption index of aerosol particles in the optical path by measuring the spectral decadic extinction coefficient at, at least, two wavelengths. In this manner it is possible, for instance, to distinguish smoke containing soot from water vapor.

  3. Inherent calibration of a novel LED-CE-DOAS instrument to measure iodine oxide, glyoxal, methyl glyoxal, nitrogen dioxide, water vapour and aerosol extinction in open cavity mode

    NASA Astrophysics Data System (ADS)

    Thalman, R.; Volkamer, R.

    2010-06-01

    The combination of Cavity Enhanced Absorption Spectroscopy (CEAS) with broad-band light sources (e.g. Light-Emitting Diodes, LEDs) lends itself to the application of cavity enhanced Differential Optical Absorption Spectroscopy (CE-DOAS) to perform sensitive and selective point measurements of multiple trace gases and aerosol extinction with a single instrument. In contrast to other broad-band CEAS techniques, CE-DOAS relies only on the measurement of relative intensity changes, i.e. does not require knowledge of the light intensity in the absence of trace gases and aerosols (I0). We have built a prototype LED-CE-DOAS instrument in the blue spectral range (420-490 nm) to measure nitrogen dioxide (NO2), glyoxal (CHOCHO), methyl glyoxal (CH3COCHO), iodine oxide (IO), water vapour (H2O) and oxygen dimers (O4). We demonstrate the first CEAS detection of methyl glyoxal, and the first CE-DOAS detection of CHOCHO and IO. A further innovation consists in the measurement of extinction losses from the cavity, e.g. due to aerosols, at two wavelengths by observing O4 (477 nm) and H2O (443 nm) and measuring the pressure, relative humidity and temperature independently. This approach is demonstrated by experiments where laboratory aerosols of known size and refractive index were generated and their extinction measured. The measured extinctions were then compared to the theoretical extinctions calculated using Mie theory (3-7×10-7 cm-1). Excellent agreement is found from both the O4 and H2O retrievals. This enables the first inherently calibrated CEAS measurement in open cavity mode (mirrors facing the open atmosphere), and eliminates the need for sampling lines to supply air to the cavity, and/or keep the cavity enclosed and aerosol free. Measurements in open cavity mode are demonstrated for CHOCHO, CH3COCHO, NO2, H2O and aerosol extinction at 477 nm and 443 nm. Our prototype LED-CE-DOAS provides a low cost, yet research grade innovative instrument for applications in simulation

  4. Use of Lidar Derived Optical Extinction and Backscattering Coefficients Near Cloud Base to Explore Aerosol-Cloud Interactions

    NASA Astrophysics Data System (ADS)

    Han, Zaw; Wu, Yonhgua; Gross, Barry; Moshary, Fred

    2016-06-01

    Combination of microwave radiometer (MWR) and mutlifilter rotating shadowband radiometer (MFRSR) measurement data together with SBDART radiative transfer model to compute cloud optical depth (COD) and cloud droplet effective radius (Reff). Quantify the first aerosol indirect effect using calculated Reff and aerosol extinction from Raman lidar measurement in urban coastal region. Illustrate comparison between ground-based and satellite retrievals. Demonstrate relationship between surface aerosol (PM2.5) loading and Reff. We also explain the sensitivity of aerosol-cloud-index (ACI) depend on the aerosol layer from cloud base height. Potential used of less noisy elastic backscattering to calculate the ACI instead of using Raman extinction. We also present comparison of elastic backscattering and Raman extinction correlation to Reff.

  5. Comparison of vertical aerosol extinction coefficients from in-situ and LIDAR measurements

    NASA Astrophysics Data System (ADS)

    Rosati, B.; Herrmann, E.; Bucci, S.; Fierli, F.; Cairo, F.; Gysel, M.; Tillmann, R.; Größ, J.; Gobbi, G. P.; Di Liberto, L.; Di Donfrancesco, G.; Wiedensohler, A.; Weingartner, E.; Virtanen, A.; Mentel, T. F.; Baltensperger, U.

    2015-07-01

    Vertical profiles of aerosol optical properties were explored in a case study near the San Pietro Capofiume (SPC) ground station during the PEGASOS Po Valley campaign in the summer of 2012. A Zeppelin NT airship was employed to investigate the effect of the dynamics of the planetary boundary layer at altitudes between ~ 50-800 m above ground. Determined properties included the aerosol size distribution, the hygroscopic growth factor, the effective index of refraction and the light absorption coefficient. The first three parameters were used to retrieve the light scattering coefficient. Simultaneously, direct measurements of both the scattering and absorption coefficient were carried out at the SPC ground station. Additionally, a LIDAR system provided aerosol extinction coefficients for a vertically resolved comparison between in-situ and remote sensing results. First, the airborne results at low altitudes were validated with the ground measurements. Agreement within approximately ±25 and ±20% was found for the dry scattering and absorption coefficient, respectively. The single scattering albedo, ranged between 0.83 to 0.95, indicating the importance of the absorbing particles in the Po Valley region. A clear layering of the atmosphere was observed during the beginning of the flight (until ~ 10 local time) before the mixed layer (ML) was fully developed. Highest extinction coefficients were found at low altitudes, in the new ML, while values in the residual layer, which could be probed at the beginning of the flight at elevated altitudes, were lower. At the end of the flight (after ~ 12 local time) the ML was fully developed, resulting in constant extinction coefficients at all altitudes measured on the Zeppelin NT. LIDAR results captured these dynamic features well and good agreement was found for the extinction coefficients compared to the in-situ results, using fixed LIDAR ratios (LR) between 30 and 70 sr for the altitudes probed with the Zeppelin. These LR are

  6. The impacts of aerosol loading, composition, and water uptake on aerosol extinction variability in the Baltimore-Washington, D.C. region

    NASA Astrophysics Data System (ADS)

    Beyersdorf, A. J.; Ziemba, L. D.; Chen, G.; Corr, C. A.; Crawford, J. H.; Diskin, G. S.; Moore, R. H.; Thornhill, K. L.; Winstead, E. L.; Anderson, B. E.

    2016-01-01

    In order to utilize satellite-based aerosol measurements for the determination of air quality, the relationship between aerosol optical properties (wavelength-dependent, column-integrated extinction measured by satellites) and mass measurements of aerosol loading (PM2.5 used for air quality monitoring) must be understood. This connection varies with many factors including those specific to the aerosol type - such as composition, size, and hygroscopicity - and to the surrounding atmosphere, such as temperature, relative humidity (RH), and altitude, all of which can vary spatially and temporally. During the DISCOVER-AQ (Deriving Information on Surface conditions from Column and Vertically Resolved Observations Relevant to Air Quality) project, extensive in situ atmospheric profiling in the Baltimore, MD-Washington, D.C. region was performed during 14 flights in July 2011. Identical flight plans and profile locations throughout the project provide meaningful statistics for determining the variability in and correlations between aerosol loading, composition, optical properties, and meteorological conditions. Measured water-soluble aerosol mass was composed primarily of ammonium sulfate (campaign average of 32 %) and organics (57 %). A distinct difference in composition was observed, with high-loading days having a proportionally larger percentage of sulfate due to transport from the Ohio River Valley. This composition shift caused a change in the aerosol water-uptake potential (hygroscopicity) such that higher relative contributions of inorganics increased the bulk aerosol hygroscopicity. These days also tended to have higher relative humidity, causing an increase in the water content of the aerosol. Conversely, low-aerosol-loading days had lower sulfate and higher black carbon contributions, causing lower single-scattering albedos (SSAs). The average black carbon concentrations were 240 ng m-3 in the lowest 1 km, decreasing to 35 ng m-3 in the free troposphere (above

  7. SAGE III Aerosol Extinction Validation in the Arctic Winter: Comparisons with SAGE II and POAM III

    NASA Technical Reports Server (NTRS)

    Thomason, L. W.; Poole, L. R.; Randall, C. E.

    2007-01-01

    The use of SAGE III multiwavelength aerosol extinction coefficient measurements to infer PSC type is contingent on the robustness of both the extinction magnitude and its spectral variation. Past validation with SAGE II and other similar measurements has shown that the SAGE III extinction coefficient measurements are reliable though the comparisons have been greatly weighted toward measurements made at mid-latitudes. Some aerosol comparisons made in the Arctic winter as a part of SOLVE II suggested that SAGE III values, particularly at longer wavelengths, are too small with the implication that both the magnitude and the wavelength dependence are not reliable. Comparisons with POAM III have also suggested a similar discrepancy. Herein, we use SAGE II data as a common standard for comparison of SAGE III and POAM III measurements in the Arctic winters of 2002/2003 through 2004/2005. During the winter, SAGE II measurements are made infrequently at the same latitudes as these instruments. We have mitigated this problem through the use potential vorticity as a spatial coordinate and thus greatly increased the number of coincident events. We find that SAGE II and III extinction coefficient measurements show a high degree of compatibility at both 1020 nm and 450 nm except a 10-20% bias at both wavelengths. In addition, the 452 to 1020-nm extinction ratio shows a consistent bias of approx. 30% throughout the lower stratosphere. We also find that SAGE II and POAM III are on average consistent though the comparisons show a much higher variability and larger bias than SAGE II/III comparisons. In addition, we find that the two data sets are not well correlated below 18 km. Overall, we find both the extinction values and the spectral dependence from SAGE III are robust and we find no evidence of a significant defect within the Arctic vortex.

  8. Optical and physical properties of stratospheric aerosols from balloon measurements in the visible and near-infrared domains. 1. Analysis of aerosol extinction spectra from the AMON and SALOMON balloonborne spectrometers.

    PubMed

    Berthet, Gwenaël; Renard, Jean-Baptiste; Brogniez, Colette; Robert, Claude; Chartier, Michel; Pirre, Michel

    2002-12-20

    Aerosol extinction coefficients have been derived in the 375-700-nm spectral domain from measurement in the stratosphere since 1992, at night, at mid- and high latitudes from 15 to 40 km, by two balloonborne spectrometers, Absorption par les Minoritaires Ozone et NO(chi) (AMON) and Spectroscopie d'Absorption Lunaire pour l'Observation des Minoritaires Ozone et NO(chi) (SALOMON). Log-normal size distributions associated with the Mie-computed extinction spectra that best fit the measurements permit calculation of integrated properties of the distributions. Although measured extinction spectra that correspond to background aerosols can be reproduced by the Mie scattering model by use of monomodal log-normal size distributions, each flight reveals some large discrepancies between measurement and theory at several altitudes. The agreement between measured and Mie-calculated extinction spectra is significantly improved by use of bimodal log-normal distributions. Nevertheless, neither monomodal nor bimodal distributions permit correct reproduction of some of the measured extinction shapes, especially for the 26 February 1997 AMON flight, which exhibited spectral behavior attributed to particles from a polar stratospheric cloud event.

  9. Optical and physical properties of stratospheric aerosols from balloon measurements in the visible and near-infrared domains. I. Analysis of aerosol extinction spectra from the AMON and SALOMON balloonborne spectrometers

    NASA Astrophysics Data System (ADS)

    Berthet, Gwenaël; Renard, Jean-Baptiste; Brogniez, Colette; Robert, Claude; Chartier, Michel; Pirre, Michel

    2002-12-01

    Aerosol extinction coefficients have been derived in the 375-700-nm spectral domain from measurements in the stratosphere since 1992, at night, at mid- and high latitudes from 15 to 40 km, by two balloonborne spectrometers, Absorption par les Minoritaires Ozone et NOx (AMON) and Spectroscopie d'Absorption Lunaire pour l'Observation des Minoritaires Ozone et NOx (SALOMON). Log-normal size distributions associated with the Mie-computed extinction spectra that best fit the measurements permit calculation of integrated properties of the distributions. Although measured extinction spectra that correspond to background aerosols can be reproduced by the Mie scattering model by use of monomodal log-normal size distributions, each flight reveals some large discrepancies between measurement and theory at several altitudes. The agreement between measured and Mie-calculated extinction spectra is significantly improved by use of bimodal log-normal distributions. Nevertheless, neither monomodal nor bimodal distributions permit correct reproduction of some of the measured extinction shapes, especially for the 26 February 1997 AMON flight, which exhibited spectral behavior attributed to particles from a polar stratospheric cloud event.

  10. Statistical analysis of the spatial-temporal distribution of aerosol extinction retrieved by micro-pulse lidar in Kashgar, China.

    PubMed

    Zhu, Wenyue; Xu, Chidong; Qian, Xianmei; Wei, Heli

    2013-02-11

    The spatial-temporal distribution of dust aerosol is important in climate model and ecological environment. An observation experiment of the aerosol vertical distribution in the low troposphere was made using the micro-pulse lidar system from Sept. 2008 to Aug. 2009 at the oasis city Kashgar, China, which is near the major dust source area of the Taklimakan desert. The monthly averaged temporal variation of aerosol extinction profiles are given in the paper. The profile of aerosol extinction coefficient suggested that the dust aerosol could be vertically transported from the ground level to the higher altitude of above 5 km around the source region, and the temporal distribution showed that the dust aerosol layer of a few hundred meters thick appeared in the seasons of early spring and summer near the ground surface.

  11. Inherent calibration of a blue LED-CE-DOAS instrument to measure iodine oxide, glyoxal, methyl glyoxal, nitrogen dioxide, water vapour and aerosol extinction in open cavity mode

    NASA Astrophysics Data System (ADS)

    Thalman, R.; Volkamer, R.

    2010-12-01

    The combination of Cavity Enhanced Absorption Spectroscopy (CEAS) with broad-band light sources (e.g. Light-Emitting Diodes, LEDs) lends itself to the application of cavity enhanced Differential Optical Absorption Spectroscopy (CE-DOAS) to perform sensitive and selective point measurements of multiple trace gases and aerosol extinction with a single instrument. In contrast to other broad-band CEAS techniques, CE-DOAS relies only on the measurement of relative intensity changes, i.e. does not require knowledge of the light intensity in the absence of trace gases and aerosols (I0). We have built a prototype LED-CE-DOAS instrument in the blue spectral range (420-490 nm) to measure nitrogen dioxide (NO2), glyoxal (CHOCHO), methyl glyoxal (CH3COCHO), iodine oxide (IO), water vapour (H2O) and oxygen dimers (O4). We demonstrate the first direct detection of methyl glyoxal, and the first CE-DOAS detection of CHOCHO and IO. The instrument is further inherently calibrated for light extinction from the cavity by observing O4 or H2O (at 477 nm and 443 nm) and measuring the pressure, relative humidity and temperature independently. This approach is demonstrated by experiments where laboratory aerosols of known size and refractive index were generated and their extinction measured. The measured extinctions were then compared to the theoretical extinctions calculated using Mie theory (3-7 × 10-7cm-1). Excellent agreement is found from both the O4 and H2O retrievals. This enables the first inherently calibrated CEAS measurement at blue wavelengths in open cavity mode, and eliminates the need for sampling lines to supply air to the cavity, i.e., keep the cavity enclosed and/or aerosol free. Measurements in open cavity mode are demonstrated for CHOCHO, CH3COCHO, NO2, H2O and aerosol extinction. Our prototype LED-CE-DOAS provides a low cost, yet research grade innovative instrument for applications in simulation chambers and in the open atmosphere.

  12. Analysis of DIAL/HSRL aerosol backscatter and extinction profiles during the SEAC4RS campaign with an aerosol assimilation system

    NASA Astrophysics Data System (ADS)

    Weaver, C. J.; da Silva, A. M., Jr.; Colarco, P. R.; Randles, C. A.

    2015-12-01

    We retrieve aerosol concentrations and optical information from vertical profiles of airborne 532 nm extinction and 532 and 1064 nm backscatter measurements made during the SEAC4RS summer 2013 campaign. The observations are from the High Spectral Resolution Lidar (HSRL) Airborne Differential Absorption Lidar (DIAL) on board the NASA DC-8. Instead of retrieving information about aerosol microphysical properties such as indexes of refraction, we seek information more directly applicable to an aerosol transport model - in our case the Goddard Chemistry Aerosol Radiation and Transport (GOCART) module used in the GEOS-5 Earth modeling system. A joint atmosphere/aerosol mini-reanalysis was performed for the SEAC4RS period using GEOS-5. The meteorological reanalysis followed the MERRA-2 atmospheric reanalysis protocol, and aerosol information from MODIS, MISR, and AERONET provided a constraint on the simulated aerosol optical depth (i.e., total column loading of aerosols). We focus on the simulated concentrations of 10 relevant aerosol species simulated by the GOCART module: dust, sulfate, and organic and black carbon. Our first retrieval algorithm starts with the SEAC4RS mini-reanalysis and adjusts the concentration of each GOCART aerosol species so that differences between the observed and simulated backscatter and extinction measurements are minimized. In this case, too often we are unable to simulate the observations by simple adjustment of the aerosol concentrations. A second retrieval approach adjusts both the aerosol concentrations and the optical parameters (i.e., assigned mass extinction efficiency) associated with each GOCART species. We present results from DC-8 flights over smoke from forest fires over the western US using both retrieval approaches. Finally, we compare our retrieved quantities with in-situ observations of aerosol absorption, scattering, and mass concentrations at flight altitude.

  13. Using Airborne High Spectral Resolution Lidar Data to Evaluate Combined Active Plus Passive Retrievals of Aerosol Extinction Profiles

    NASA Technical Reports Server (NTRS)

    Burton, S. P.; Ferrare, R. A.; Hostetler, C. A.; Hair, J. W.; Kittaka, C.; Vaughn, M. A.; Remer, L. A.

    2010-01-01

    We derive aerosol extinction profiles from airborne and space-based lidar backscatter signals by constraining the retrieval with column aerosol optical thickness (AOT), with no need to rely on assumptions about aerosol type or lidar ratio. The backscatter data were acquired by the NASA Langley Research Center airborne High Spectral Resolution Lidar (HSRL) and by the Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP) instrument on the Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observation (CALIPSO) satellite. The HSRL also simultaneously measures aerosol extinction coefficients independently using the high spectral resolution lidar technique, thereby providing an ideal data set for evaluating the retrieval. We retrieve aerosol extinction profiles from both HSRL and CALIOP attenuated backscatter data constrained with HSRL, Moderate-Resolution Imaging Spectroradiometer (MODIS), and Multiangle Imaging Spectroradiometer column AOT. The resulting profiles are compared with the aerosol extinction measured by HSRL. Retrievals are limited to cases where the column aerosol thickness is greater than 0.2 over land and 0.15 over water. In the case of large AOT, the results using the Aqua MODIS constraint over water are poorer than Aqua MODIS over land or Terra MODIS. The poorer results relate to an apparent bias in Aqua MODIS AOT over water observed in August 2007. This apparent bias is still under investigation. Finally, aerosol extinction coefficients are derived from CALIPSO backscatter data using AOT from Aqua MODIS for 28 profiles over land and 9 over water. They agree with coincident measurements by the airborne HSRL to within +/-0.016/km +/- 20% for at least two-thirds of land points and within +/-0.028/km +/- 20% for at least two-thirds of ocean points.

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

    NASA Astrophysics Data System (ADS)

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

    2014-12-01

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

  15. Aerosol extinction properties over coastal West Bengal Gangetic plain under inter-seasonal and sea breeze influenced transport processes

    NASA Astrophysics Data System (ADS)

    Verma, S.; Priyadharshini, B.; Pani, S. K.; Bharath Kumar, D.; Faruqi, A. R.; Bhanja, S. N.; Mandal, M.

    2016-01-01

    We analysed the atmospheric aerosol extinction properties under an influence of inter-seasonal and sea breeze (SB) transport processes over coastal West Bengal (WB) Gangetic plain (WBGP). The predominant frequency of airmass back trajectory path was through the Arabian Sea (AS) during southwest monsoon (SWmon) and that through the Indo-Gangetic plain (IGP) during transition to winter (Twin) season and the Bay of Bengal during transition to summer (Tsumm) season. Aerosol surface concentration (Sconc) and aerosol extinction exhibited heterogeneity in the seasonal variability over coastal WBGP with their highest seasonal mean being during winter and summer seasons respectively. Seasonal mean extinction was respectively 17% and 30% higher during winter and summer seasons than that during SWmon. While angstrom exponent (AE) was less than one during SWmon, Tsumm, and summer seasons, it was near to one during Twin and winter monsoon (Wmon), and was more than one during winter season. Relative contribution (%) of upper (at altitude above 1 km) aerosol layer (UAL) to aerosol extinction during summer was four times of that during winter. Seasonally distinct vertical distribution of aerosol extinction associated with meteorological and SB influenced transport and that due to influence of high rise open burning emissions was inferred. Possible aerosol subtypes extracted during days in Tsumm were inferred to be mostly constituted of dust and polluted dust during daytime, in addition to polluted continental and smoke in UAL during nighttime. In contrast to that at nearby urban location (Kolkata, KOL), intensity of updraft of airmass evaluated during evening/SB activity hour (1730 local time, (LT)) at study site (Kharagpur, KGP) was as high as 3.5 times the intensity during near to noon hour (1130 LT); this intensity was the highest along coast of westBengal-Orissa. Enhanced Sconc and relative contribution of UAL to aerosol extinction (58% compared to 36% only at nearby urban

  16. Modeling of growth and evaporation effects on the extinction of 1.0-micron solar radiation traversing stratospheric sulfuric acid aerosols

    NASA Technical Reports Server (NTRS)

    Yue, G. K.; Deepak, A.

    1981-01-01

    The effects of growth and evaporation of stratospheric sulfuric acid aerosols on the extinction of solar radiation traversing such an aerosol medium are reported for the case of 1.0-micron solar radiation. Modeling results show that aerosol extinction is not very sensitive to the change of ambient water vapor concentration, but is sensitive to ambient temperature changes, especially at low ambient temperatures and high ambient water vapor concentration. A clarification is given of the effects of initial aerosol size distribution and composition on the change of aerosol extinction due to growth and evaporation processes. It is shown that experiments designed to observe solar radiation extinction of aerosols may also be applied to the determination of observed changes in aerosol optical properties, environmental parameters, or the physical and optical characteristics of sulfate aerosols.

  17. In situ infrared aerosol spectroscopy for a variety of nerve agent simulants using flow-through photoacoustics

    NASA Astrophysics Data System (ADS)

    Gurton, Kristan P.; Felton, Melvin; Dahmani, Rachid; Ligon, David

    2007-09-01

    We present newly measured results of an ongoing experimental program established to measure optical cross sections in the mid- and long-wave infrared for a variety of chemically and biologically based aerosols. For this study we consider only chemically derived aerosols, and in particular, a group of chemical compounds often used as simulants for the detection of extremely toxic organophosphorus nerve agents. These materials include: diethyl methylphosphonate (DEMP), dimethyl methylphosphonate (DMMP), diisopropyl methylphosphonate (DIMP), and diethyl phthalate (DEP). As reported in a prior study [Appl. Opt. 44, 4001 (2005)], we combine two optical techniques well suited for aerosol spectroscopy [i.e., flow-through photoacoustics and Fourier transform infrared (FTIR) emission spectroscopy], to measure in situ the absolute extinction and absorption cross sections over a variety of wavelengths spanning the IR spectral region from 3 to 13 μm. Aerosol size distribution(s), particle number density, and dosimetric measurements are recorded simultaneously in order to present optical cross sections that are aerosol mass normalized, i.e., m2/gram. Photoacoustic results, conducted at a series of CO2 laser lines, compare well with measured broadband FTIR spectral extinction. Both FTIR and photoacoustic data also compare well with Mie theory calculations based on measured size distributions and previously published complex indices of refraction.

  18. Measurement of aerosol optical properties by cw cavity enhanced spectroscopy

    NASA Astrophysics Data System (ADS)

    Jie, Guo; Ye, Shan-Shan; Yang, Xiao; Han, Ye-Xing; Tang, Huai-Wu; Yu, Zhi-Wei

    2016-10-01

    The CAPS (Cavity Attenuated Phase shift Spectroscopy) system, which detects the extinction coefficients within a 10 nm bandpass centered at 532 nm, comprises a green LED with center wavelength in 532nm, a resonant optical cavity (36 cm length), a Photo Multiplier Tube detector, and a lock in amplifier. The square wave modulated light from the LED passes through the optical cavity and is detected as a distorted waveform which is characterized by a phase shift with respect to the initial modulation. Extinction coefficients are determined from changes in the phase shift of the distorted waveform of the square wave modulated LED light that is transmitted through the optical cavity. The performance of the CAPS system was evaluated by using measurements of the stability and response of the system. The minima ( 0.1 Mm-1) in the Allan plots show the optimum average time ( 100s) for optimum detection performance of the CAPS system. In the paper, it illustrates that extinction coefficient was correlated with PM2.5 mass (0.91). These figures indicate that this method has the potential to become one of the most sensitive on-line analytical techniques for extinction coefficient detection. This work aims to provide an initial validation of the CAPS extinction monitor in laboratory and field environments. Our initial results presented in this paper show that the CAPS extinction monitor is capable of providing state-of-the-art performance while dramatically reducing the complexity of optical instrumentation for directly measuring the extinction coefficients.

  19. 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.

  20. Studying the vertical aerosol extinction coefficient by comparing in situ airborne data and elastic backscatter lidar

    NASA Astrophysics Data System (ADS)

    Rosati, Bernadette; Herrmann, Erik; Bucci, Silvia; Fierli, Federico; Cairo, Francesco; Gysel, Martin; Tillmann, Ralf; Größ, Johannes; Gobbi, Gian Paolo; Di Liberto, Luca; Di Donfrancesco, Guido; Wiedensohler, Alfred; Weingartner, Ernest; Virtanen, Annele; Mentel, Thomas F.; Baltensperger, Urs

    2016-04-01

    Vertical profiles of aerosol particle optical properties were explored in a case study near the San Pietro Capofiume (SPC) ground station during the PEGASOS Po Valley campaign in the summer of 2012. A Zeppelin NT airship was employed to investigate the effect of the dynamics of the planetary boundary layer at altitudes between ˜ 50 and 800 m above ground. Determined properties included the aerosol particle size distribution, the hygroscopic growth factor, the effective index of refraction and the light absorption coefficient. The first three parameters were used to retrieve the light scattering coefficient. Simultaneously, direct measurements of both the scattering and absorption coefficient were carried out at the SPC ground station. Additionally, a single wavelength polarization diversity elastic lidar system provided estimates of aerosol extinction coefficients using the Klett method to accomplish the inversion of the signal, for a vertically resolved comparison between in situ and remote-sensing results. Note, however, that the comparison was for the most part done in the altitude range where the overlap function is incomplete and accordingly uncertainties are larger. First, the airborne results at low altitudes were validated with the ground measurements. Agreement within approximately ±25 and ±20 % was found for the dry scattering and absorption coefficient, respectively. The single scattering albedo, ranged between 0.83 and 0.95, indicating the importance of the absorbing particles in the Po Valley region. A clear layering of the atmosphere was observed during the beginning of the flight (until ˜ 10:00 LT - local time) before the mixing layer (ML) was fully developed. Highest extinction coefficients were found at low altitudes, in the new ML, while values in the residual layer, which could be probed at the beginning of the flight at elevated altitudes, were lower. At the end of the flight (after ˜ 12:00 LT) the ML was fully developed, resulting in

  1. How well can we Measure the Vertical Profile of Tropospheric Aerosol Extinction?

    NASA Technical Reports Server (NTRS)

    Schmid, Beat; Ferrare, R.; Flynn, C.; Elleman, R.; Covert, D.; Strawa, A.; Welton, E.; Turner, D.; Jonsson, H.; Redemann, J.

    2005-01-01

    The recent Department of Energy Atmospheric Radiation Measurement (ARM) Aerosol Intensive Operations Period (MOP, May 2003) yielded one of the best measurement sets obtained to-date to assess our ability to measure the vertical profile of ambient aerosol extinction sigma(sub ep)(lambda) in the lower troposphere. During one month, a heavily instrumented aircraft with well characterized aerosol sampling ability carrying well proven and new aerosol instrumentation, devoted most of the 60 available flight hours to flying vertical profiles over the heavily instrumented ARM Southern Great Plains (SGP) Climate Research Facility (CRF). This allowed us to compare vertical extinction profiles obtained from 6 different instuments: airborne Sun photometer (AATS-14), airborne nephelometer/absorption photometer, airborne cavity ring-down system, ground-based Raman lidar and 2 ground-based elastic backscatter lidars. We find the in-situ measured sigma(sub ep)(lambda) to be lower than the AATS-14 derived values. Bias differences are 0.002 - 0.004 K/m equivalent to 12-17% in the visible, or 45% in the near-infrared. On the other hand, we find that with respect to AATS-14, the lidar sigma(sub ep)(lambda) are higher. An unnoticed loss of sensitivity of the Raman lidar had occurred leading up to AIOP and we expect better agreement from the recently restored system looking at the collective results from 6 field campaigns conducted since 1996, airborne in situ measurements of sigma(sub ep)(lambda) tend to be biased slightly low (17% at visible wavelengths) when compared to airborne Sun photometer sigma(sub ep)(lambda). On the other hand, sigma(sub ep)(lambda) values derived from lidars tend to have no or positive biases. From the bias differences we conclude that the typical systematic error associated with measuring the tropospheric vertical profile of the ambient aerosol extinction with current state of-the art instrumentation is 15-20% at visible wavelengths and potentially larger in

  2. Infrared extinction spectra of mineral dust aerosol: Single components and complex mixtures

    NASA Astrophysics Data System (ADS)

    Laskina, Olga; Young, Mark A.; Kleiber, Paul D.; Grassian, Vicki H.

    2012-09-01

    Simultaneous Fourier transform infrared (FTIR) extinction spectra and aerosol size distributions have been measured for some components of mineral dust aerosol including feldspars (albite, oligoclase) and diatomaceous earth, as well as more complex authentic dust samples that include Iowa loess and Saharan sand. Spectral simulations for single-component samples, derived from Rayleigh-theory models for characteristic particle shapes, better reproduce the experimental spectra including the peak position and band shape compared to Mie theory. The mineralogy of the authentic dust samples was inferred using analysis of FTIR spectra. This approach allows for analysis of the mineralogy of complex multicomponent dust samples. Extinction spectra for the authentic dust samples were simulated from the derived sample mineralogy using published optical constant data for the individual mineral constituents and assuming an external mixture. Nonspherical particle shape effects were also included in the simulations and were shown to have a significant effect on the results. The results show that the position of the peak and the shape of the band of the IR characteristic features in the 800 to 1400 cm-1 spectral range are not well simulated by Mie theory. The resonance peaks are consistently shifted by more than +40 cm-1 relative to the experimental spectrum in the Mie simulation. Rayleigh model solutions for different particle shapes better predict the peak position and band shape of experimental spectra, even though the Rayleigh condition may not be strictly obeyed in these experiments.

  3. Characterization of urban aerosol using aerosol mass spectrometry and proton nuclear magnetic resonance spectroscopy

    NASA Astrophysics Data System (ADS)

    Cleveland, M. J.; Ziemba, L. D.; Griffin, R. J.; Dibb, J. E.; Anderson, C. H.; Lefer, B.; Rappenglück, B.

    2012-07-01

    Particulate matter was measured during August and September of 2006 in Houston as part of the Texas Air Quality Study II Radical and Aerosol Measurement Project. Aerosol size and composition were determined using an Aerodyne quadrupole aerosol mass spectrometer. Aerosol was dominated by sulfate (4.1 ± 2.6 μg m-3) and organic material (5.5 ± 4.0 μg m-3), with contributions of organic material from both primary (˜32%) and secondary (˜68%) sources. Secondary organic aerosol appears to be formed locally. In addition, 29 aerosol filter samples were analyzed using proton nuclear magnetic resonance (1H NMR) spectroscopy to determine relative concentrations of organic functional groups. Houston aerosols are less oxidized than those observed elsewhere, with smaller relative contributions of carbon-oxygen double bonds. These particles do not fit 1H NMR source apportionment fingerprints for identification of secondary, marine, and biomass burning organic aerosol, suggesting that a new fingerprint for highly urbanized and industrially influenced locations be established.

  4. The CU Airborne MAX-DOAS instrument: ground based validation, and vertical profiling of aerosol extinction and trace gases

    NASA Astrophysics Data System (ADS)

    Baidar, S.; Oetjen, H.; Coburn, S.; Dix, B.; Ortega, I.; Sinreich, R.; Volkamer, R.

    2012-09-01

    The University of Colorado Airborne Multi Axis Differential Optical Absorption Spectroscopy (CU AMAX-DOAS) instrument uses solar stray light remote sensing to detect and quantify multiple trace gases, including nitrogen dioxide (NO2), glyoxal (CHOCHO), formaldehyde (HCHO), water vapor (H2O), nitrous acid (HONO), iodine monoxide (IO), bromine monoxide (BrO), and oxygen dimers (O4) at multiple wavelengths (360 nm, 477 nm, 577 nm and 632 nm) simultaneously, and sensitively in the open atmosphere. The instrument is unique, in that it presents the first systematic implementation of MAX-DOAS on research aircraft, i.e. (1) includes measurements of solar stray light photons from nadir, zenith, and multiple elevation angles forward and below the plane by the same spectrometer/detector system, and (2) features a motion compensation system that decouples the telescope field of view (FOV) from aircraft movements in real-time (< 0.35° accuracy). Sets of solar stray light spectra collected from nadir to zenith scans provide some vertical profile information within 2 km above and below the aircraft altitude, and the vertical column density (VCD) below the aircraft is measured in nadir view. Maximum information about vertical profiles is derived simultaneously for trace gas concentrations and aerosol extinction coefficients over similar spatial scales and with a vertical resolution of typically 250 m during aircraft ascent/descent. The instrument is described, and data from flights over California during the CalNex and CARES air quality field campaigns is presented. Horizontal distributions of NO2 VCDs (below the aircraft) maps are sampled with typically 1 km resolution, and show good agreement with two ground based CU MAX-DOAS instruments (slope 0.95 ± 0.09, R2 = 0.86). As a case study vertical profiles of NO2, CHOCHO, HCHO, and H2O mixing ratios and aerosol extinction coefficients, ɛ, at 477nm calculated from O4 measurements from a low approach at Brackett airfield inside the

  5. Statistics of aerosol extinction coefficient profiles and optical depth using lidar measurement over Lanzhou, China since 2005-2008

    NASA Astrophysics Data System (ADS)

    Cao, X.; Wang, Z.; Tian, P.; Wang, J.; Zhang, L.; Quan, X.

    2013-06-01

    The aerosol extinction coefficient profiles and optical depth over Lanzhou in China were observed under no precipitation and dust free condition using the micropulse lidar CE370-2 from September 2005 to July 2008. The statistics of the variations of monthly average aerosol optical depth (AOD) and daily average AOD, frequency distribution of daily average AOD, and the seasonal variation of aerosol vertical distribution were analyzed based on the observation data. The results showed that the daily average AOD of Main Observatory and City Observatory was 87.8% and 78.2% ranged below 0.4 respectively with similar frequency distribution patterns. The AOD in autumn and winter were larger than that in spring and summer, and AOD in suburb was in certain extent smaller than that in city of Lanzhou. Aerosol existed in the layer below 4km, and its extinction coefficient decreased with increasing of height.

  6. Retrieval of aerosol refractive index from extinction spectra with a damped harmonic-oscillator band model.

    PubMed

    Thomas, Gareth E; Bass, Stephen F; Grainger, Roy G; Lambert, Alyn

    2005-03-01

    A new method for the retrieval of the spectral refractive indices of micrometer-sized particles from infrared aerosol extinction spectra has been developed. With this method we use a classical damped harmonic-oscillator model of molecular absorption in conjunction with Mie scattering to model extinction spectra, which we then fit to the measurements using a numerical optimal estimation algorithm. The main advantage of this method over the more traditional Kramers-Kronig approach is that it allows the full complex refractive-index spectra, along with the parameters of the particle size distribution, to be retrieved from a single extinction spectrum. The retrieval scheme has been extensively characterized and has been found to provide refractive indices with a maximum uncertainty of approximately 10% (with a minimum of approximately 0.1%). Comparison of refractive indices calculated from measurements of a ternary solution of HNO3, H2SO4, and H2O with those published in J. Phys. Chem. A 104, 783 (2000) show similar differences as found by other authors.

  7. Characterization and source apportionment of aerosol light extinction with a coupled model of CMB-IMPROVE in Hangzhou, Yangtze River Delta of China

    NASA Astrophysics Data System (ADS)

    Wang, Jiao; Zhang, Yu-fen; Feng, Yin-chang; Zheng, Xian-jue; Jiao, Li; Hong, Sheng-mao; Shen, Jian-dong; Zhu, Tan; Ding, Jing; Zhang, Qi

    2016-09-01

    To investigate the characteristics and sources of aerosol light extinction in the Yangtze River Delta of China, a campaign was carried out in Hangzhou from December 2013 to November 2014. Hourly data for air pollutants including PM2.5, SO2, NO2, O3 and CO, and aerosol optical properties including aerosol scattering coefficient and aerosol absorbing coefficient was obtained in the environmental air quality automatic monitoring station. Meteorological parameters were measured synchronously in the automated meteorology monitoring station. Additionally, around seven sets of ambient PM2.5 samples per month were collected and analyzed during the campaign. The annual mean aerosol scattering coefficient, aerosol absorbing coefficient and aerosol single scattering albedo measured in this study was 514 ± 284 Mm- 1, 35 ± 20 Mm- 1 and 94% respectively. The aerosol extinction coefficient reconstructed using the modified IMPROVE (Interagency Monitoring of Protected Visual Environment) formula was compared to the measured extinction coefficient. Better correlations could be found between the measured and reconstructed extinction coefficient when RH was under 90%. A coupled model of CMB (chemical mass balance) and modified IMPROVE was used to apportion the sources of aerosol light extinction in Hangzhou. Vehicle exhaust, secondary nitrate and secondary sulfate were identified as the most significant sources for aerosol light extinction, accounted for 30.2%, 24.1% and 15.8% respectively.

  8. 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.

  9. Retrieval of Aerosol Profiles using Multi Axis Differential Absorption Spectroscopy (MAX-DOAS)

    NASA Astrophysics Data System (ADS)

    Yilmaz, S.; Friess, U.; Apituley, A.; de Leeuw, G.; Platt, U.

    2009-04-01

    Multi Axis Differential Absorption Spectroscopy (MAX-DOAS) is a well established measurement technique to derive atmospheric trace gas profiles. Using MAX-DOAS measurements of trace gases with a known vertical profile, like the oxygen-dimer O4, it is possible to retrieve information on atmospheric aerosols. Based on the optimal estimation method, we have developed an algorithm which fits simultaneously measured O4 optical densities at several wavelengths and elevation angles to values simulated by a radiative transfer model. Retrieval parameters are aerosol extinction profile and optical properties like single scattering albedo, phase function and Angström exponent. In the scope of a joint research activity of the EU funded project EUSAAR (European Supersites for Atmospheric Aerosol Research) we have developed a new kind of DOAS instrument, which uses three miniature spectrometers to cover the near-ultraviolet to visible wavelength range (290-790nm), enabling to capture all absorption bands of the oxygen-dimer O4. Additionally, it is possible to point to any direction in the sky with a 2D telescope unit which is connected to the spectrometers via fiber optics. In May 2008, an intercomparison campaign with established aerosol measurement techniques took place in Cabauw/Netherlands, where simultaneous DOAS, LIDAR, Sun photometer and Nephelometer measurements were performed. We present first results of selected days from this period. The optical properties of aerosols retrieved by the DOAS measurement technique show very promising qualitative agreement with the established measurement techniques demonstrating the progress towards our goal of establishing the MAX-DOAS technique for retrieving optical properties of atmospheric aerosols. Quantitative comparison is ongoing.

  10. In situ vertical profiles of aerosol extinction, mass, and composition over the southeast United States during SENEX and SEAC4RS: observations of a modest aerosol enhancement aloft

    NASA Astrophysics Data System (ADS)

    Wagner, N. L.; Brock, C. A.; Angevine, W. M.; Beyersdorf, A.; Campuzano-Jost, P.; Day, D. A.; de Gouw, J. A.; Diskin, G. S.; Gordon, T. D.; Graus, M. G.; Huey, G.; Jimenez, J. L.; Lack, D. A.; Liao, J.; Liu, X.; Markovic, M. Z.; Middlebrook, A. M.; Mikoviny, T.; Peischl, J.; Perring, A. E.; Richardson, M. S.; Ryerson, T. B.; Schwarz, J. P.; Warneke, C.; Welti, A.; Wisthaler, A.; Ziemba, L. D.; Murphy, D. M.

    2015-02-01

    Vertical profiles of submicron aerosol over the southeastern United States (SEUS) during the summertime from in situ aircraft-based measurements were used to construct aggregate profiles of chemical, microphysical, and optical properties. Shallow cumulus convection was observed during many profiles. These conditions enhance vertical transport of trace gases and aerosol and create a cloudy transition layer on top of the sub-cloud mixed layer. The trace gas and aerosol concentrations in the transition layer were modeled as a mixture with contributions from the mixed layer below and the free troposphere above. The amount of vertical mixing, or entrainment of air from the free troposphere, was quantified using the observed mixing ratio of carbon monoxide (CO). Although the median aerosol mass, extinction, and volume decreased with altitude in the transition layer, they were ~10% larger than expected from vertical mixing alone. This enhancement was likely due to secondary aerosol formation in the transition layer. Although the transition layer enhancements of the particulate sulfate and organic aerosol (OA) were both similar in magnitude, only the enhancement of sulfate was statistically significant. The column integrated extinction, or aerosol optical depth (AOD), was calculated for each individual profile, and the transition layer enhancement of extinction typically contributed less than 10% to the total AOD. Our measurements and analysis were motivated by two recent studies that have hypothesized an enhanced layer of secondary organic aerosol (SOA) aloft to explain the summertime enhancement of AOD (2-3 times greater than winter) over the southeastern United States. In contrast to this hypothesis, the modest enhancement we observed in the transition layer was not dominated by OA and was not a large fraction of the summertime AOD.

  11. 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].

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

    NASA Astrophysics Data System (ADS)

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

    2014-12-01

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

  13. On the accuracy of stratospheric aerosol extinction derived from in situ size distribution measurements and surface area density derived from remote SAGE II and HALOE extinction measurements

    SciTech Connect

    Kovilakam, Mahesh; Deshler, Terry

    2015-08-26

    In situ stratospheric aerosol measurements, from University of Wyoming optical particle counters (OPCs), are compared with Stratospheric Aerosol Gas Experiment (SAGE) II (versions 6.2 and 7.0) and Halogen Occultation Experiment (HALOE) satellite measurements to investigate differences between SAGE II/HALOE-measured extinction and derived surface area and OPC-derived extinction and surface area. Coincident OPC and SAGE II measurements are compared for a volcanic (1991-1996) and nonvolcanic (1997 2005) period. OPC calculated extinctions agree with SAGE II measurements, within instrumental uncertainty, during the volcanic period, but have been a factor of 2 low during the nonvolcanic period. Three systematic errors associated with the OPC measurements, anisokineticity, inlet particle evaporation, and counting efficiency, were investigated. An overestimation of the OPC counting efficiency is found to be the major source of systematic error. With this correction OPC calculated extinction increases by 15 30% (30 50%) for the volcanic (nonvolcanic) measurements. These changes significantly improve the comparison with SAGE II and HALOE extinctions in the nonvolcanic cases but slightly degrade the agreement in the volcanic period. These corrections have impacts on OPC-derived surface area density, exacerbating the poor agreement between OPC and SAGE II (version 6.2) surface areas. This disparity is reconciled with SAGE II version 7.0 surface areas. For both the volcanic and nonvolcanic cases these changes in OPC counting efficiency and in the operational SAGE II surface area algorithm leave the derived surface areas from both platforms in significantly better agreement and within the 40% precision of the OPC moment calculations.

  14. On the accuracy of stratospheric aerosol extinction derived from in situ size distribution measurements and surface area density derived from remote SAGE II and HALOE extinction measurements

    DOE PAGES

    Kovilakam, Mahesh; Deshler, Terry

    2015-08-26

    In situ stratospheric aerosol measurements, from University of Wyoming optical particle counters (OPCs), are compared with Stratospheric Aerosol Gas Experiment (SAGE) II (versions 6.2 and 7.0) and Halogen Occultation Experiment (HALOE) satellite measurements to investigate differences between SAGE II/HALOE-measured extinction and derived surface area and OPC-derived extinction and surface area. Coincident OPC and SAGE II measurements are compared for a volcanic (1991-1996) and nonvolcanic (1997 2005) period. OPC calculated extinctions agree with SAGE II measurements, within instrumental uncertainty, during the volcanic period, but have been a factor of 2 low during the nonvolcanic period. Three systematic errors associated with themore » OPC measurements, anisokineticity, inlet particle evaporation, and counting efficiency, were investigated. An overestimation of the OPC counting efficiency is found to be the major source of systematic error. With this correction OPC calculated extinction increases by 15 30% (30 50%) for the volcanic (nonvolcanic) measurements. These changes significantly improve the comparison with SAGE II and HALOE extinctions in the nonvolcanic cases but slightly degrade the agreement in the volcanic period. These corrections have impacts on OPC-derived surface area density, exacerbating the poor agreement between OPC and SAGE II (version 6.2) surface areas. This disparity is reconciled with SAGE II version 7.0 surface areas. For both the volcanic and nonvolcanic cases these changes in OPC counting efficiency and in the operational SAGE II surface area algorithm leave the derived surface areas from both platforms in significantly better agreement and within the 40% precision of the OPC moment calculations.« less

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

    SciTech Connect

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

    2016-01-01

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

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

    DOE PAGES

    Feng, Y.; Kotamarthi, V. R.; Coulter, R.; ...

    2015-06-19

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

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

    SciTech Connect

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

    2015-06-19

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

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

    DOE PAGES

    Feng, Y.; Kotamarthi, V. R.; Coulter, R.; ...

    2016-01-18

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

  19. VUV spectroscopy of carbon dust analogs: contribution to interstellar extinction

    NASA Astrophysics Data System (ADS)

    Gavilan, L.; Alata, I.; Le, K. C.; Pino, T.; Giuliani, A.; Dartois, E.

    2016-02-01

    Context. A full spectral characterization of carbonaceous dust analogs is necessary to understand their potential as carriers of observed astronomical spectral signatures such as the ubiquitous UV bump at 217.5 nm and the far-ultraviolet (FUV) rise common to interstellar extinction curves. Aims: Our goal is to study the spectral properties of carbonaceous dust analogs from the FUV to the mid-infrared (MIR) domain. We seek in particular to understand the spectra of these materials in the FUV range, for which laboratory studies are scarce. Methods: We produced analogs to carbonaceous interstellar dust encountered in various phases of the interstellar medium: amorphous hydrogenated carbons (a-C:H), for carbonaceous dust observed in the diffuse interstellar medium, and soot particles, for the polyaromatic component. Analogs to a-C:H dust were produced using a radio-frequency plasma reactor at low pressures, and soot nanoparticles films were produced in an ethylene (C2H4) flame. We measured transmission spectra of these thin films (thickness <100 nm) in the far-ultraviolet (190-250 nm) and in the vacuum-ultraviolet (VUV; 50-190 nm) regions using the APEX chamber at the DISCO beam line of the SOLEIL synchrotron radiation facility. These were also characterized through infrared microscopy at the SMIS beam line. Results: We successfully measured the transmission spectra of these analogs from λ = 1 μm to 50 nm. From these, we extracted the laboratory optical constants via Kramers-Kronig inversion. We used these constants for comparison to existing interstellar extinction curves. Conclusions: We extend the spectral measurements of these types of carbonaceous analogs into the VUV and link the spectral features in this range to the 3.4 μm band. We suggest that these two materials might contribute to different classes of interstellar extinction curves.

  20. AerGOM, an improved algorithm for stratospheric aerosol extinction retrieval from GOMOS observations - Part 2: Intercomparisons

    NASA Astrophysics Data System (ADS)

    Étienne Robert, Charles; Bingen, Christine; Vanhellemont, Filip; Mateshvili, Nina; Dekemper, Emmanuel; Tétard, Cédric; Fussen, Didier; Bourassa, Adam; Zehner, Claus

    2016-09-01

    AerGOM is a retrieval algorithm developed for the GOMOS instrument onboard Envisat as an alternative to the operational retrieval (IPF). AerGOM enhances the quality of the stratospheric aerosol extinction retrieval due to the extension of the spectral range used, refines the aerosol spectral parameterization, the simultaneous inversion of all atmospheric species as well as an improvement of the Rayleigh scattering correction. The retrieval algorithm allows for a good characterization of the stratospheric aerosol extinction for a wide range of wavelengths.In this work, we present the results of stratospheric aerosol extinction comparisons between AerGOM and various spaceborne instruments (SAGE II, SAGE III, POAM III, ACE-MAESTRO and OSIRIS) for different wavelengths. The aerosol extinction intercomparisons for λ < 700 nm and above 20 km show agreements with SAGE II version 7 and SAGE III version 4.0 within ±15 % and ±45 %, respectively. There is a strong positive bias below 20 km at λ < 700 nm, which suggests that cirrus clouds at these altitudes have a large impact on the extinction values. Comparisons performed with GOMOS IPF v6.01 alongside AerGOM show that at short wavelengths and altitudes below 20 km, IPF retrievals are more accurate when evaluated against SAGE II and SAGE III but are much less precise than AerGOM. A modified aerosol spectral parameterization can improve AerGOM in this spectral and altitude range and leads to results that have an accuracy similar to IPF retrievals. Comparisons of AerGOM aerosol extinction coefficients with OSIRIS and SAGE III measurements at wavelengths larger than 700 nm show a very large negative bias at altitudes above 25 km. Therefore, the use of AerGOM aerosol extinction data is not recommended for λ > 700 nm.Due to the unique observational technique of GOMOS, some of the results appear to be dependent on the star occultation parameters such as star apparent temperature and magnitude, solar zenith angle

  1. In situ vertical profiles of aerosol extinction, mass, and composition over the southeast United States during SENEX and SEAC4RS: observations of a modest aerosol enhancement aloft

    NASA Astrophysics Data System (ADS)

    Wagner, N. L.; Brock, C. A.; Angevine, W. M.; Beyersdorf, A.; Campuzano-Jost, P.; Day, D.; de Gouw, J. A.; Diskin, G. S.; Gordon, T. D.; Graus, M. G.; Holloway, J. S.; Huey, G.; Jimenez, J. L.; Lack, D. A.; Liao, J.; Liu, X.; Markovic, M. Z.; Middlebrook, A. M.; Mikoviny, T.; Peischl, J.; Perring, A. E.; Richardson, M. S.; Ryerson, T. B.; Schwarz, J. P.; Warneke, C.; Welti, A.; Wisthaler, A.; Ziemba, L. D.; Murphy, D. M.

    2015-06-01

    Vertical profiles of submicron aerosol from in situ aircraft-based measurements were used to construct aggregate profiles of chemical, microphysical, and optical properties. These vertical profiles were collected over the southeastern United States (SEUS) during the summer of 2013 as part of two separate field studies: the Southeast Nexus (SENEX) study and the Study of Emissions and Atmospheric Composition, Clouds, and Climate Coupling by Regional Surveys (SEAC4RS). Shallow cumulus convection was observed during many profiles. These conditions enhance vertical transport of trace gases and aerosol and create a cloudy transition layer on top of the sub-cloud mixed layer. The trace gas and aerosol concentrations in the transition layer were modeled as a mixture with contributions from the mixed layer below and the free troposphere above. The amount of vertical mixing, or entrainment of air from the free troposphere, was quantified using the observed mixing ratio of carbon monoxide (CO). Although the median aerosol mass, extinction, and volume decreased with altitude in the transition layer, they were ~10 % larger than expected from vertical mixing alone. This enhancement was likely due to secondary aerosol formation in the transition layer. Although the transition layer enhancements of the particulate sulfate and organic aerosol (OA) were both similar in magnitude, only the enhancement of sulfate was statistically significant. The column integrated extinction, or aerosol optical depth (AOD), was calculated for each individual profile, and the transition layer enhancement of extinction typically contributed less than 10 % to the total AOD. Our measurements and analysis were motivated by two recent studies that have hypothesized an enhanced layer of secondary aerosol aloft to explain the summertime enhancement of AOD (2-3 times greater than winter) over the southeastern United States. The first study attributes the layer aloft to secondary organic aerosol (SOA) while

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

    NASA Technical Reports Server (NTRS)

    Pepin, T. J.

    1977-01-01

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

  3. Evaluating Nighttime CALIOP 0.532 micron Aerosol Optical Depth and Extinction Coefficient Retrievals

    NASA Technical Reports Server (NTRS)

    Campbell, J. R.; Tackett, J. L.; Reid, J. S.; Zhang, J.; Curtis, C. A.; Hyer, E. J.; Sessions, W. R.; Westphal, D. L.; Prospero, J. M.; Welton, E. J.; Omar, A. H.; Vaughan, M. A.; Winker, D. M.

    2012-01-01

    NASA Cloud Aerosol Lidar with Orthogonal Polarization (CALIOP) Version 3.01 5-km nighttime 0.532 micron aerosol optical depth (AOD) datasets from 2007 are screened, averaged and evaluated at 1 deg X 1 deg resolution versus corresponding/co-incident 0.550 micron AOD derived using the US Navy Aerosol Analysis and Prediction System (NAAPS), featuring two-dimensional variational assimilation of quality-assured NASA Moderate Resolution Imaging Spectroradiometer (MODIS) and Multi-angle Imaging Spectroradiometer (MISR) AOD. In the absence of sunlight, since passive radiometric AOD retrievals rely overwhelmingly on scattered radiances, the model represents one of the few practical global estimates available from which to attempt such a validation. Daytime comparisons, though, provide useful context. Regional-mean CALIOP vertical profiles of night/day 0.532 micron extinction coefficient are compared with 0.523/0.532 micron ground-based lidar measurements to investigate representativeness and diurnal variability. In this analysis, mean nighttime CALIOP AOD are mostly lower than daytime (0.121 vs. 0.126 for all aggregated data points, and 0.099 vs. 0.102 when averaged globally per normalised 1 deg. X 1 deg. bin), though the relationship is reversed over land and coastal regions when the data are averaged per normalised bin (0.134/0.108 vs. 0140/0.112, respectively). Offsets assessed within single bins alone approach +/- 20 %. CALIOP AOD, both day and night, are higher than NAAPS over land (0.137 vs. 0.124) and equal over water (0.082 vs. 0.083) when averaged globally per normalised bin. However, for all data points inclusive, NAAPS exceeds CALIOP over land, coast and ocean, both day and night. Again, differences assessed within single bins approach 50% in extreme cases. Correlation between CALIOP and NAAPS AOD is comparable during both day and night. Higher correlation is found nearest the equator, both as a function of sample size and relative signal magnitudes inherent at

  4. Composition of the Martian aerosols through near-IR spectroscopy

    NASA Technical Reports Server (NTRS)

    Erard, Stephane; Cerroni, Priscilla; Coradini, Angioletta

    1993-01-01

    Near-infrared spectroscopy is a powerful technique to study the composition of planetary surfaces, as the main minerals exhibit absorption bands in this spectral range. It gave important information on the mineralogy and petrology of Mars in the past twenty years although in this case it is well known that a large fraction of light is scattered by the airborne particles before reaching the surface. The measured signal is thus the sum of two different contributions that should be studied separately: One from the surface and one from the aerosols that depends on their density, size distribution and composition. Data from the ISM imaging spectrometer are used here to derive the aerosols spectrum. They consist in sets of spectra (from 0.76 to 3.16 microns) of approximately 3000 pixels approximately 25x25 sq km in size. The resulting spectrum exhibits both water-ice and clay mineral features superimposed on a scattering continuum.

  5. How much information do extinction and backscattering measurements contain about the chemical composition of atmospheric aerosol?

    NASA Astrophysics Data System (ADS)

    Kahnert, Michael; Andersson, Emma

    2017-03-01

    We theoretically and numerically investigate the problem of assimilating multiwavelength lidar observations of extinction and backscattering coefficients of aerosols into a chemical transport model. More specifically, we consider the inverse problem of determining the chemical composition of aerosols from these observations. The main questions are how much information the observations contain to determine the particles' chemical composition, and how one can optimize a chemical data assimilation system to make maximum use of the available information. We first quantify the information content of the measurements by computing the singular values of the scaled observation operator. From the singular values we can compute the number of signal degrees of freedom, Ns, and the reduction in Shannon entropy, H. As expected, the information content as expressed by either Ns or H grows as one increases the number of observational parameters and/or wavelengths. However, the information content is strongly sensitive to the observation error. The larger the observation error variance, the lower the growth rate of Ns or H with increasing number of observations. The right singular vectors of the scaled observation operator can be employed to transform the model variables into a new basis in which the components of the state vector can be partitioned into signal-related and noise-related components. We incorporate these results in a chemical data assimilation algorithm by introducing weak constraints that restrict the assimilation algorithm to acting on the signal-related model variables only. This ensures that the information contained in the measurements is fully exploited, but not overused. Numerical tests show that the constrained data assimilation algorithm provides a solution to the inverse problem that is considerably less noisy than the corresponding unconstrained algorithm. This suggests that the restriction of the algorithm to the signal-related model variables suppresses

  6. Ultra-high spectral extinction Brillouin spectroscopy for turbid tissue measurements (Conference Presentation)

    NASA Astrophysics Data System (ADS)

    Zhang, Jitao; Fiore, Antonio; Shao, Peng; Yun, Seok-Hyun; Scarcelli, Giuliano

    2016-03-01

    Brillouin spectroscopy allows non-invasive measurement of the mechanical properties of a sample by measuring the spectra of acoustically induced light scattering therein, and thus has been widely investigated for biomedical application. Recently, the development of fast Brillouin spectrometry based on virtually-imaged phased array (VIPA) has made in-situ measurement of biomedical sample possible. However, one limitation of current Brillouin technique is the low spectral extinction, which limits the measurement to nearly transparent sample. In order to measure turbid sample, multistage VIPA can be cascaded to gain spectral extinction. For example, spectral extinction of ~80 dB was achieved using three-stage VIPA; however, this approach significantly sacrificed measurement throughput. In this work, we develop a novel spectrometer that achieves high extinction without significant signal loss. To achieve this goal, we combine a two-stage VIPA spectrometer with a triple-pass Fabry-Perot interferometer. The triple-pass Fabry-Perot interferometer acts as a band-pass filter with ~3 GHz bandwidth and ~35-dB spectral extinction. Therefore, the overall extinction of this spectrometer greatly surpasses 80 dB with only ~20% excess loss. We demonstrated the performance of this spectrometer measuring background-free Brillouin spectra from Intralipid solutions and within chicken tissue.

  7. Vertical distribution of ambient aerosol extinctive properties during haze and haze-free periods based on the Micro-Pulse Lidar observation in Shanghai.

    PubMed

    Liu, Qiong; He, Qianshan; Fang, Sihua; Guang, Ying; Ma, Chengyu; Chen, Yonghang; Kang, Yanming; Pan, Hu; Zhang, Hua; Yao, Yifeng

    2017-01-01

    Ambient aerosols make a significant contribution to the environment and climate through their optical properties. In this study, the aerosol extinction coefficient and Aerosol optical depth (AOD) retrieved using the Fernald Method from the ground-based Micro-Pulse Lidar (MPL) were used to investigate the characteristics of aerosols during haze and haze-free periods in Shanghai. There were 216 haze days including 145 dry haze days, 39 damp haze days and 32days of both dry and damp haze in Shanghai from March 2009 to February 2010. During the haze periods, aerosols were concentrated mainly below 600m resulting in the most severe pollution layer in Shanghai. In contrast to the aerosol optical properties during haze-free periods, aerosol extinction coefficients and AOD were larger in the lower altitude (below 1km) during haze periods. The lowest 1km contributed 53-72% of the Aerosol optical depth (AOD) below 6km for the haze periods and <41% of that for the haze-free periods except summer. According to the analysis of influencing factors, although atmospheric convection was strong in summer which led to reduce the extinction, the highest occurrence of haze with relatively low aerosol extinction most of time was in summer, which resulted from the factors such as higher relative humidity, temperature and more solar radiation causing hygroscopic growth of particles and formation of secondary aerosols; in spring and autumn, there was less haze occurrences because the boundary layer was relatively higher, which allowed pollutants to diffuse more easily, but spring was the second most frequency season of haze due to frequent dust transport from the north; in winter high concentrations of particles and low boundary layer height were not beneficial to the diffusion of pollutants near the surface and caused haze occurrence rather high with high aerosol extinction.

  8. 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.

  9. Optical properties of urban aerosols, aircraft emissions, and heavy-duty diesel trucks using aerosol light extinction measurements by an Aerodyne Cavity Attenuated Phase Shift Particle Extinction Monitor (CAPS PMex)

    NASA Astrophysics Data System (ADS)

    Freedman, A.; Massoli, P.; Wood, E. C.; Allan, J. D.; Fortner, E.; Yu, Z.; Herndon, S. C.; Miake-Lye, R. C.; Onasch, T. B.

    2010-12-01

    We present results of optical property characterization of ambient particulate during several field deployments where measurements of aerosol light extinction (σep) are obtained using an Aerodyne Cavity Attenuated Phase Shift Particle Extinction Monitor (CAPS PMex). The CAPS PMex is able to provide extinction measurements with 3-σ detection limit of 3 Mm-1 for 1s integration time. The CAPS PMex (630 nm) is integrated in the Aerodyne Research, Inc. (ARI) mobile laboratory where a co-located Multi Angle Absorption Photometer (MAAP) provides particle light absorption coefficient at 632 nm. The combination of the CAPS with the MAAP data allows estimating the single scattering albedo (ω) of the ambient aerosol particles. The ARI mobile laboratory was deployed in winter 2010 at the Chicago O’Hare International Airport to measure gas phase and particulate emissions from different aircraft engines, and during summer 2010 in Oakland, CA, to characterize vehicular gaseous and particulate emissions (mainly exhaust from heavy-duty diesel trucks) from the Caldecott Tunnel. We provide estimates of black carbon emission factors from individual aircraft engines and diesel trucks, in addition to characterizing the optical properties of these ambient samples studying fleet-average emissions for both light-duty passenger vehicles and heavy-duty diesel trucks. Two CAPS PMex instruments (measuring σep at 630 and 532 nm) were also deployed during the CalNex 2010 study (May 14 - June 16) at the CalTech ground site in Pasadena, CA. During the same time, a photo-acoustic spectrometer (PAS, DMT) and an aethalometer instrument (Magee Sci.) measured particle light absorption of submicron aerosol particles from the same sample line as the CAPS PMex monitors. We combine these data to provide multi-wavelength ω trends for the one-month campaign. Our results show the high potential of the CAPS as light weight, compact instrument to perform precise and accurate σep measurements of

  10. Investigating vertical distributions of ozone and of the aerosol extinction coefficient in the middle atmosphere with the MKS-M and SFN-4 instruments on board Salyut-7

    NASA Astrophysics Data System (ADS)

    Badaev, V. V.; Grechko, G. M.; Elanskii, N. F.; Kan, V.; Plotkin, M. E.

    1989-04-01

    The technical characteristics of the multichannel spectrometer (MKS-M) system combined with a camera containing a spectrophotography attachment (SFN-4) are discussed together with results obtained by this system on distributions of ozone and aerosol in the middle atmosphere. It is demonstrated that this system is capable of retrieving the fine structure of vertical ozone and aerosol extinction distributions in the lower stratosphere. Results show that, in the ozonosphere, the contents of ozone and of aerosol exhibit a negative correlation.

  11. Broadband optical extinction measurements and complex refractive indices in the ultraviolet spectral region for biogenic secondary organic aerosol exposed to ammonia

    NASA Astrophysics Data System (ADS)

    Flores, J.; Washenfelder, R. A.; Lee, H.; Segev, L.; Nizkorodov, S.; Brown, S. S.; Rudich, Y.

    2013-12-01

    The interaction between aerosols and sunlight plays an important role in the radiative balance of Earth's atmosphere. Aerosols can both scatter and absorb solar radiation causing surface cooling and heating of the atmosphere. These interactions depend on the optical properties of the aerosols (i.e., complex refractive index). Secondary organic aerosol (SOA) account for a significant fraction of the tropospheric aerosol. However, their chemical, physical, and optical properties, especially as they are processed in the atmosphere (aging), are still poorly understood. In this study, SOA formed by the ozonolysis of various biogenic volatile organic compound (BVOC) precursors (α-pinene, limonene, and α-humulene) were exposed to humid air containing various concentrations of gaseous ammonia which has been shown to cause the biogenic SOA to ';brown' on filters. The extent of absorption of the SOA in the aerosol phase cause by the exposure to gaseous ammonia was measured by a newly developed instrument to measure aerosol extinction as a function of wavelength using Broadband Cavity Enhanced Spectroscopy (BBCES) with a broadband light source. Size-selected measurements of the humid SOA exposed to NH3 for about 1.5 hours were used to derive complex refractive indices (RI) as a function of wavelength in the UV spectral region (from 360 - 420nm). The imaginary part of the refractive index did not exceed 0.05 in the 360 - 420 nm range for SOA formed from the three BVOCs even at high concentrations of NH3 (>1ppm), allowing to place an upper limit of k = 0.05. Furthermore, the small k values are consistent with bulk UV-VIS measurements. However, for the α-pinene SOA, the real part of the RI slightly increased from n = 1.49 to n = 1.55 with negligible spectral dependence. For limonene and α-humulene the real part remind constant within error calculations. Based on these observations, reactive uptake of gaseous ammonia is not expected to significantly affect absorption and

  12. Development of an Internet accessible software: optics and spectroscopy of gas-aerosol media

    NASA Astrophysics Data System (ADS)

    Voitsekhovskaya, O. K.; Kashirskii, D. E.; Egorov, O. V.

    2015-11-01

    A description of an Internet accessible software «Optics and spectroscopy of gas-aerosol media» is represented. The new software is focused on research in the field of direct and inverse problems of optics and spectroscopy of gas-aerosol media.

  13. AerGOM, an improved algorithm for stratospheric aerosol extinction retrieval from GOMOS observations - Part 1: Algorithm description

    NASA Astrophysics Data System (ADS)

    Vanhellemont, Filip; Mateshvili, Nina; Blanot, Laurent; Étienne Robert, Charles; Bingen, Christine; Sofieva, Viktoria; Dalaudier, Francis; Tétard, Cédric; Fussen, Didier; Dekemper, Emmanuel; Kyrölä, Erkki; Laine, Marko; Tamminen, Johanna; Zehner, Claus

    2016-09-01

    The GOMOS instrument on Envisat has successfully demonstrated that a UV-Vis-NIR spaceborne stellar occultation instrument is capable of delivering quality data on the gaseous and particulate composition of Earth's atmosphere. Still, some problems related to data inversion remained to be examined. In the past, it was found that the aerosol extinction profile retrievals in the upper troposphere and stratosphere are of good quality at a reference wavelength of 500 nm but suffer from anomalous, retrieval-related perturbations at other wavelengths. Identification of algorithmic problems and subsequent improvement was therefore necessary. This work has been carried out; the resulting AerGOM Level 2 retrieval algorithm together with the first data version AerGOMv1.0 forms the subject of this paper. The AerGOM algorithm differs from the standard GOMOS IPF processor in a number of important ways: more accurate physical laws have been implemented, all retrieval-related covariances are taken into account, and the aerosol extinction spectral model is strongly improved. Retrieval examples demonstrate that the previously observed profile perturbations have disappeared, and the obtained extinction spectra look in general more consistent. We present a detailed validation study in a companion paper; here, to give a first idea of the data quality, a worst-case comparison at 386 nm shows SAGE II-AerGOM correlation coefficients that are up to 1 order of magnitude larger than the ones obtained with the GOMOS IPFv6.01 data set.

  14. UV/Visible Aerosol Extinction Measurements performed by GOMOS onboard ENVISAT: results for the period August 2002 to March 2005.

    NASA Astrophysics Data System (ADS)

    Vanhellemont, F.; Fussen, D.; Dodion, J.; Bingen, C.; Mateshvili, N.; Gomos Team

    Launched in March 2002 the GOMOS Global Ozone Monitoring by Occultation of Stars instrument onboard the European Envisat satellite has already provided a wealth of information on the geographical and temporal distribution of several atmospheric species Vertical profiles for these species are numerically retrieved from measurements of starlight that is transmitted through the atmosphere at different tangent altitudes The actual spectrum at each tangent altitude is measured within the UV Visible wavelength range Typically within the useful range from 248 nm to 690 nm gas concentration profiles for O 3 NO 2 H 2 O neutral air and aerosol extinction profiles can be retrieved Although stars are relatively weak light sources the advantage of the star occultation lies in the fact that useful stars are available at all times during orbit As a consequence GOMOS has measured more than 300 000 occultations in the considered period from August 2002 to March 2005 In this work we present results for the aerosol extinction retrievals Using selection criteria for different occultation properties such as the star magnitude and the illumination conditions a subset of reliable occultations were picked Subsequently a spatial and temporal binning was performed and data were averaged The resulting climatology provides a good view on the spatial distribution and temporal evolution of aerosols in the stratosphere Special attention is given to the presence of PSCs in the Antarctic polar vortex and equatorial cirrus clouds First results on particle sizes

  15. Four-year long-path monitoring of ambient aerosol extinction at a central European urban site: dependence on relative humidity

    NASA Astrophysics Data System (ADS)

    Skupin, A.; Ansmann, A.; Engelmann, R.; Seifert, P.; Müller, T.

    2016-02-01

    The ambient aerosol particle extinction coefficient is measured with the Spectral Aerosol Extinction Monitoring System (SÆMS) along a 2.84 km horizontal path at 30-50 m height above ground in the urban environment of Leipzig (51.3° N, 12.4° E), Germany, since 2009. The dependence of the particle extinction coefficient (wavelength range from 300 to 1000 nm) on relative humidity up to almost 100 % was investigated. The main results are presented. For the wavelength of 550 nm, the mean extinction enhancement factor was found to be 1.75 ± 0.4 for an increase of relative humidity from 40 to 80 %. The respective 4-year mean extinction enhancement factor is 2.8 ± 0.6 for a relative-humidity increase from 40 to 95 %. A parameterization of the dependency of the urban particle extinction coefficient on relative humidity is presented. A mean hygroscopic exponent of 0.46 for the 2009-2012 period was determined. Based on a backward trajectory cluster analysis, the dependence of several aerosol optical properties for eight air flow regimes was investigated. Large differences were not found, indicating that local pollution sources widely control the aerosol conditions over the urban site. The comparison of the SÆMS extinction coefficient statistics with respective statistics from ambient AERONET sun photometer observations yields good agreement. Also, time series of the particle extinction coefficient computed from in situ-measured dry particle size distributions and humidity-corrected SÆMS extinction values (for 40 % relative humidity) were found in good overall consistency, which verifies the applicability of the developed humidity parameterization scheme. The analysis of the spectral dependence of particle extinction (Ångström exponent) revealed an increase of the 390-881 nm Ångström exponent from, on average, 0.3 (at 30 % relative humidity) to 1.3 (at 95 % relative humidity) for the 4-year period.

  16. Aerosol collection and analysis using diffuse reflectance infrared spectroscopy

    NASA Astrophysics Data System (ADS)

    Samuels, Alan C.; Wong, Diane M.; Meyer, Gerald J.; Roelant, Geoffrey J.; Williams, Barry R.; Miles, Ronald W., Jr.; Manning, Christopher J.

    2004-08-01

    Infrared spectroscopy is routinely employed for the identification of organic molecules and, more recently, for the classification of biological materials. We have developed a sample collection method that facilitates infrared analysis of airborne particulates using a diffuse reflectance (DR) technique. Efforts are underway to extend the method to include simultaneous analysis of vapor phase organics by using adsorbent substrates compatible with the DR technique. This series of laboratory results provides proof-of-principle for both the sample collection and data collection processes. Signal processing of the DR spectra is shown to provide rapid qualitative identification of representative aerosol materials, including particulate matter commonly found in the environment. We compare the results for such materials as bacterial spores, pollens and molds, clays and dusts, smoke and soot. Background correction analysis is shown to be useful for differentiation and identification of these constituents. Issues relating to complex mixtures of environmental samples under highly variable conditions are considered. Instrumentation development and materials research are now underway with the aim of constructing a compact sampling system for near real-time monitoring of aerosol and organic pollutants. A miniature, tilt-compensated Fourier transform spectrometer will provide spectroscopic interrogation. A series of advanced digital signal processing methods are also under development to enhance the sensor package. The approach will be useful for industrial applications, chemical and biological agent detection, and environmental monitoring for chemical vapors, hazardous air pollutants, and allergens.

  17. CU AMAX-DOAS applications in cloud-free and cloudy atmospheres: innovative Scattered Sun Light observations of trace gases and aerosol extinction

    NASA Astrophysics Data System (ADS)

    Volkamer, R.; Baidar, S.; Coburn, S.; Dix, B. K.; Oetjen, H.; Ortega, I.; Sinreich, R.; Atmospeclab

    2011-12-01

    An innovative airborne scanning multi-axis differential optical absorption spectroscopy (CU AMAX-DOAS) instrument has been developed at the University of Colorado, Boulder. The instrument collects scattered sunlight spectra in a sequence of discrete viewing angles, and employs the DOAS method (inherently calibrated, and selective) to simultaneously retrieve multiple trace gases, e.g., nitrogen dioxide (NO2), nitrous acid (HONO), formaldehyde (HCHO), glyoxal (CHOCHO), bromine oxide (BrO), iodine oxide (IO), chlorine dioxide (OClO), water vapor (H2O), and oxygen dimers (O4, at 360nm, 477nm, and 632nm) differential slant column densities (dSCD). Vertical profiles of these gases and multi-spectral aerosol extinction are inferred by combining Monte-Carlo Radiative Transfer Modelling (RTM) and optimal estimation techniques to construct a model atmosphere that can in principle represent 3D clouds and aerosols. The atmospheric state of this model atmosphere is constrained by observations of O4 dSCDs, Raman Scattering Probability (RSP), and intensity ratios, i.e., quantities that depend solely on relative intensity changes, without need for a direct sun view, or absolute radiance calibration. We show results from ongoing validation efforts (NOAA TwinOtter aircraft during CalNex and CARES), and demonstrate vertical profile retrievals (NSF/NCAR GV over the tropical Pacific Ocean) in both cloud-free and cloudy atmospheres.

  18. Verification and application of the extended spectral deconvolution algorithm (SDA+) methodology to estimate aerosol fine and coarse mode extinction coefficients in the marine boundary layer

    NASA Astrophysics Data System (ADS)

    Kaku, K. C.; Reid, J. S.; O'Neill, N. T.; Quinn, P. K.; Coffman, D. J.; Eck, T. F.

    2014-10-01

    The spectral deconvolution algorithm (SDA) and SDA+ (extended SDA) methodologies can be employed to separate the fine and coarse mode extinction coefficients from measured total aerosol extinction coefficients, but their common use is currently limited to AERONET (AErosol RObotic NETwork) aerosol optical depth (AOD). Here we provide the verification of the SDA+ methodology on a non-AERONET aerosol product, by applying it to fine and coarse mode nephelometer and particle soot absorption photometer (PSAP) data sets collected in the marine boundary layer. Using data sets collected on research vessels by NOAA-PMEL(National Oceanic and Atmospheric Administration - Pacific Marine Environmental Laboratory), we demonstrate that with accurate input, SDA+ is able to predict the fine and coarse mode scattering and extinction coefficient partition in global data sets representing a range of aerosol regimes. However, in low-extinction regimes commonly found in the clean marine boundary layer, SDA+ output accuracy is sensitive to instrumental calibration errors. This work was extended to the calculation of coarse and fine mode scattering coefficients with similar success. This effort not only verifies the application of the SDA+ method to in situ data, but by inference verifies the method as a whole for a host of applications, including AERONET. Study results open the door to much more extensive use of nephelometers and PSAPs, with the ability to calculate fine and coarse mode scattering and extinction coefficients in field campaigns that do not have the resources to explicitly measure these values.

  19. Study of MPLNET-Derived Aerosol Climatology over Kanpur, India, and Validation of CALIPSO Level 2 Version 3 Backscatter and Extinction Products

    NASA Technical Reports Server (NTRS)

    Misra, Amit; Tripathi, S. N.; Kaul, D. S.; Welton, Ellsworth J.

    2012-01-01

    The level 2 aerosol backscatter and extinction profiles from the NASA Micropulse Lidar Network (MPLNET) at Kanpur, India, have been studied from May 2009 to September 2010. Monthly averaged extinction profiles from MPLNET shows high extinction values near the surface during October March. Higher extinction values at altitudes of 24 km are observed from April to June, a period marked by frequent dust episodes. Version 3 level 2 Cloud Aerosol Lidar with Orthogonal Polarization (CALIOP) aerosol profile products have been compared with corresponding data from MPLNET over Kanpur for the above-mentioned period. Out of the available backscatter profiles, the16 profiles used in this study have time differences less than 3 h and distances less than 130 km. Among these profiles, four cases show good comparison above 400 m with R2 greater than 0.7. Comparison with AERONET data shows that the aerosol type is properly identified by the CALIOP algorithm. Cloud contamination is a possible source of error in the remaining cases of poor comparison. Another source of error is the improper backscatter-to-extinction ratio, which further affects the accuracy of extinction coefficient retrieval.

  20. Measurement of elemental concentration of aerosols using spark emission spectroscopy.

    PubMed

    Diwakar, Prasoon K; Kulkarni, Pramod

    A coaxial microelectrode system has been used to collect and analyse the elemental composition of aerosol particles in near real-time using spark emission spectroscopy. The technique involves focused electrostatic deposition of charged aerosol particles onto the flat tip of a microelectrode, followed by introduction of spark discharge. A pulsed spark discharge was generated across the electrodes with input energy ranging from 50 to 300 mJ per pulse, resulting in the formation of controlled pulsed plasma. The particulate matter on the cathode tip is ablated and atomized by the spark plasma, resulting in atomic emissions which are subsequently recorded using a broadband optical spectrometer for element identification and quantification. The plasma characteristics were found to be very consistent and reproducible even after several thousands of spark discharges using the same electrode system. The spark plasma was characterized by measuring the excitation temperature (~7000 to 10 000 K), electron density (~10(16) cm(-3)), and evolution of spectral responses as a function of time. The system was calibrated using particles containing Pb, Si, Na and Cr. Absolute mass detection limits in the range 11 pg to 1.75 ng were obtained. Repeatability of spectral measurements varied from 2 to 15%. The technique offers key advantages over similar microplasma-based techniques such as laser-induced breakdown spectroscopy, as: (i) it does not require any laser beam optics and eliminates any need for beam alignment, (ii) pulse energy from dc power supply in SIBS system can be much higher compared to that from laser source of the same physical size, and (iii) it is quite conducive to compact, field-portable instrumentation.

  1. Initial investigation of the wavelength dependence of optical properties measured with a new multi-pass Aerosol Extinction Differential Optical Absorption Spectrometer (AE-DOAS)

    NASA Astrophysics Data System (ADS)

    Chartier, R. T.; Greenslade, M. E.

    2012-04-01

    Atmospheric aerosols directly affect climate by scattering and absorbing radiation. The magnitude of the impact is dependent upon the wavelength of light, but is often estimated near 550 nm. When light scattering and absorption by aerosols is approximated, the wavelength dependence of the refractive index for specific components is lost. As a result, climate models would have inherent uncertainties for aerosol contributions to radiative forcing when considering the entire solar spectrum. An aerosol extinction differential optical absorption spectrometer has been developed to directly measure aerosol extinction at mid-ultraviolet to near infrared wavelengths. The instrument consists of a spectrometer coupled to a closed White-type multi-pass gas cell with an adjustable path length of up to approximately 20 m. Laboratory measurements of various gases are compared with known absorption cross sections. Additionally, the extinction of monodisperse samples of polystyrene latex spheres are measured and compared to Mie theory generated with refractive index values from the literature to validate the new instrument. The polystyrene experiments also emphasize the ability of the new instrument to retrieve the wavelength dependent refractive index, especially in the ultraviolet wavelength regions where variability is expected. The spectrometer will be a significant advancement for determining wavelength dependent complex refractive indices in future laboratory studies as well as provide the ability to monitor ambient aerosol light extinction.

  2. Initial investigation of the wavelength dependence of optical properties measured with a new multi-pass aerosol extinction differential optical absorption spectrometer (AE-DOAS)

    NASA Astrophysics Data System (ADS)

    Chartier, R. T.; Greenslade, M. E.

    2011-10-01

    Atmospheric aerosols directly affect climate by scattering and absorbing radiation. The magnitude of the impact is dependent upon the wavelength of light, but is often estimated near 550 nm. When light scattering and absorption by aerosols is approximated, the wavelength dependence of the refractive index for specific components is lost. As a result, climate models would have inherent uncertainties for aerosol contributions to radiative forcing when considering the entire solar spectrum. An aerosol extinction differential optical absorption spectrometer has been developed to directly measure aerosol extinction at mid-ultraviolet to near infrared wavelengths. The instrument consists of a spectrometer coupled to a closed White-type multi-pass gas cell with an adjustable path length of up to approximately 20 m. Laboratory measurements of various gases are compared with known absorption cross sections. Additionally, the extinction of monodisperse samples of polystyrene latex spheres are measured and compared to Mie theory generated with refractive index values from the literature to validate the new instrument. The polystyrene experiments also emphasize the ability of the new instrument to retrieve the wavelength dependent refractive index, especially in the ultraviolet wavelength regions where variability is expected. The spectrometer will be a significant advancement for determining wavelength dependent complex refractive indices in future laboratory studies as well as provide the ability to monitor ambient aerosol light extinction.

  3. A broadband cavity-enhanced spectrometer for measuring the extinction of aerosols at blue and near-UV wavelengths

    NASA Astrophysics Data System (ADS)

    Venables, Dean; Fullam, Donovan; Hoa Le, Phuoc; Chen, Jun; Böge, Olaf; Herrmann, Hartmut

    2016-04-01

    We describe a new broadband cavity-enhanced absorption spectrometer for sensitive extinction measurements of aerosols. The instrument is distinguished by its broad and continuous spectral coverage from the near-UV to blue wavelengths (ca. 320 to 450 nm). The short wavelength region has been little explored compared to visible wavelengths, but is important because (1) brown carbon (BrC) absorbs strongly in this wavelength region, and (2) absorption of near-UV radiation in the atmosphere alters the photolysis rate of the key atmospheric species O3, NO2, and HONO, with implications for air quality and atmospheric oxidation capacity. The instrument performance and the effect of a switchable in-line filter are characterised. Early results using the instrument in the TROPOS atmospheric simulation chamber are presented. These experiments include studies of secondary organic aerosol formation (SOA), and biomass burning experiments of rice and wheat straw, followed by experiments simulating particle aging under daytime and nighttime conditions.

  4. How Well do State-of-the-Art Techniques Measuring the Vertical Profile of Tropospheric Aerosol Extinction Compare?

    NASA Technical Reports Server (NTRS)

    Schmid, B.; Ferrare, R.; Flynn, C.; Elleman, R.; Covert, D.; Strawa, A.; Welton, E.; Turner, D.; Jonsson, H.; Redemann, J.; Eilers, J.; Ricci, K.; Hallar, A. G.; Clayton, M.; Michalsky, J.; Smirnov, A.; Holben, B.; Barnard, J.

    2006-01-01

    The recent Department of Energy Atmospheric Radiation Measurement (ARM) Aerosol Intensive Operations Period (AIOP, May 2003) yielded one of the best measurement sets obtained to date to assess our ability to measure the vertical profile of ambient aerosol extinction sigma(ep)(lambda) in the lower troposphere. During one month, a heavily instrumented aircraft with well-characterized aerosol sampling ability carrying well-proven and new aerosol instrumentation devoted most of the 60 available flight hours to flying vertical profiles over the heavily instrumented ARM Southern Great Plains (SGP) Climate Research Facility (CRF). This allowed us to compare vertical extinction profiles obtained from six different instruments: airborne Sun photometer (AATS-14), airborne nephelometer/absorption photometer, airborne cavity ring-down system, groundbased Raman lidar, and two ground-based elastic backscatter lidars. We find the in situ measured sigma(ep)(lambda) to be lower than the AATS-14 derived values. Bias differences are 0.002-0.004 Km!1 equivalent to 13-17% in the visible, or 45% in the near-infrared. On the other hand, we find that with respect to AATS-14, the lidar sigma(ep)(lambda) are higher: Bias differences are 0.004 Km(-1) (13%) and 0.007 Km(-1) (24%) for the two elastic backscatter lidars (MPLNET and MPLARM, lambda = 523 nm) and 0.029 Km(-1) (54%) for the Raman lidar (lambda = 355 nm). An unnoticed loss of sensitivity of the Raman lidar had occurred leading up to AIOP, and we expect better agreement from the recently restored system. Looking at the collective results from six field campaigns conducted since 1996, airborne in situ measurements of sigma(ep)(lambda) tend to be biased slightly low (17% at visible wavelengths) when compared to airborne Sun photometer sigma(ep)(lambda). On the other hand, sigma(ep)(lambda) values derived from lidars tend to have no or positive biases. From the bias differences we conclude that the typical systematic error associated

  5. Extinction coefficient (1 micrometer) properties of high-altitude clouds from solar occultation measurements (1985-1990): Evidence of volcanic aerosol effect

    NASA Technical Reports Server (NTRS)

    Wang, Pi-Huan; Minnis, Patrick; Yue, Glenn K.

    1995-01-01

    The properties of the 1-micrometer volume extinction coefficient of two geographically different high-altitude cloud systems have been examined for the posteruption period (1985-1990) of the April 1982 El Chichon volcanic event with emphasis on the effect of volcanic aerosols on clouds. These two high-altitude cloud systems are the tropical clouds in the tropopause region observed by the Stratospheric Aerosol and Gas Experiment (SAGE) 2 and the polar stratospheric clouds (PSCs) sighted by the Stratospheric Aerosol Measurement (SAM) 2. The results indicate that volcanic aerosols alter the frequency distributions of these high-altitude clouds in such a manner that the occurrence of clouds having high extinction coefficients (6 x 10(exp -3) - 2 x 10(exp -2)/km) is suppressed, while that of clouds having low extinction coefficients (2 x 10(exp -3) - 6 x 10(exp -2)/km) is enhanced. This influence of the volcanic aerosols appears to be opposite to the increase in the extinction coefficient of optically thick clouds observed by the Earth Radiation Budget Experiment (ERBE) during the initial posteruption period of the June 1991 Pinatubo eruption. A plausible explanation of this difference, based on the Mie theory, is presented. As a consequence of the Mie theory, the effective radius of most, if not all, of the high-altitude clouds, measured by the SAGE series of satellite instruments must be less than about 0.8 micrometers. This mean cloud particle size implied by the satellite extinction-coefficient data at a single wavelength (1 micrometer) is further substantiated by the particle size analysis based on cloud extinction coefficient at two wavelengths (0.525 and 1.02 micrometers) obtained by the SAGE 2 observations. Most of the radiation measured by ERBE is reflected by cloud systems comprised of particles having effective radii much greater than 1 micrometer. A reduction in the effective radius of these clouds due to volcanic aerosols is expected to increase their

  6. An Accuracy Assessment of the CALIOP/CALIPSO Version 2/Version 3 Daytime Aerosol Extinction Product Based on a Detailed Multi-Sensor, Multi-Platform Case Study

    NASA Technical Reports Server (NTRS)

    Kacenelenbogen, M.; Vaughan, M. A.; Redemann, J.; Hoff, R. M.; Rogers, R. R.; Ferrare, R. A.; Russell, P. B.; Hostetler, C. A.; Hair, J. W.; Holben, B. N.

    2011-01-01

    The Cloud Aerosol LIdar with Orthogonal Polarization (CALIOP), on board the CALIPSO platform, has measured profiles of total attenuated backscatter coefficient (level 1 products) since June 2006. CALIOP s level 2 products, such as the aerosol backscatter and extinction coefficient profiles, are retrieved using a complex succession of automated algorithms. The goal of this study is to help identify potential shortcomings in the CALIOP version 2 level 2 aerosol extinction product and to illustrate some of the motivation for the changes that have been introduced in the next version of CALIOP data (version 3, released in June 2010). To help illustrate the potential factors contributing to the uncertainty of the CALIOP aerosol extinction retrieval, we focus on a one-day, multi-instrument, multiplatform comparison study during the CALIPSO and Twilight Zone (CATZ) validation campaign on 4 August 2007. On that day, we observe a consistency in the Aerosol Optical Depth (AOD) values recorded by four different instruments (i.e. spaceborne MODerate Imaging Spectroradiometer, MODIS: 0.67 and POLarization and Directionality of Earth s Reflectances, POLDER: 0.58, airborne High Spectral Resolution Lidar, HSRL: 0.52 and ground-based AErosol RObotic NETwork, AERONET: 0.48 to 0.73) while CALIOP AOD is a factor of two lower (0.32 at 532 nm). This case study illustrates the following potential sources of uncertainty in the CALIOP AOD: (i) CALIOP s low signal-to-noise ratio (SNR) leading to the misclassification and/or lack of aerosol layer identification, especially close to the Earth s surface; (ii) the cloud contamination of CALIOP version 2 aerosol backscatter and extinction profiles; (iii) potentially erroneous assumptions of the aerosol extinction-to-backscatter ratio (Sa) used in CALIOP s extinction retrievals; and (iv) calibration coefficient biases in the CALIOP daytime attenuated backscatter coefficient profiles. The use of version 3 CALIOP extinction retrieval for our case

  7. An accuracy assessment of the CALIOP/CALIPSO version 2/version 3 daytime aerosol extinction product based on a detailed multi-sensor, multi-platform case study

    NASA Astrophysics Data System (ADS)

    Kacenelenbogen, M.; Vaughan, M. A.; Redemann, J.; Hoff, R. M.; Rogers, R. R.; Ferrare, R. A.; Russell, P. B.; Hostetler, C. A.; Hair, J. W.; Holben, B. N.

    2011-04-01

    The Cloud Aerosol LIdar with Orthogonal Polarization (CALIOP), on board the CALIPSO platform, has measured profiles of total attenuated backscatter coefficient (level 1 products) since June 2006. CALIOP's level 2 products, such as the aerosol backscatter and extinction coefficient profiles, are retrieved using a complex succession of automated algorithms. The goal of this study is to help identify potential shortcomings in the CALIOP version 2 level 2 aerosol extinction product and to illustrate some of the motivation for the changes that have been introduced in the next version of CALIOP data (version 3, released in June 2010). To help illustrate the potential factors contributing to the uncertainty of the CALIOP aerosol extinction retrieval, we focus on a one-day, multi-instrument, multiplatform comparison study during the CALIPSO and Twilight Zone (CATZ) validation campaign on 4 August 2007. On that day, we observe a consistency in the Aerosol Optical Depth (AOD) values recorded by four different instruments (i.e. space-borne MODerate Imaging Spectroradiometer, MODIS: 0.67 and POLarization and Directionality of Earth's Reflectances, POLDER: 0.58, airborne High Spectral Resolution Lidar, HSRL: 0.52 and ground-based AErosol RObotic NETwork, AERONET: 0.48 to 0.73) while CALIOP AOD is a factor of two lower (0.32 at 532 nm). This case study illustrates the following potential sources of uncertainty in the CALIOP AOD: (i) CALIOP's low signal-to-noise ratio (SNR) leading to the misclassification and/or lack of aerosol layer identification, especially close to the Earth's surface; (ii) the cloud contamination of CALIOP version 2 aerosol backscatter and extinction profiles; (iii) potentially erroneous assumptions of the aerosol extinction-to-backscatter ratio (Sa) used in CALIOP's extinction retrievals; and (iv) calibration coefficient biases in the CALIOP daytime attenuated backscatter coefficient profiles. The use of version 3 CALIOP extinction retrieval for our case

  8. Phase function, backscatter, extinction, and absorption for standard radiation atmosphere and El Chichon aerosol models at visible and near-infrared wavelengths

    NASA Technical Reports Server (NTRS)

    Whitlock, C. H.; Suttles, J. T.; Lecroy, S. R.

    1985-01-01

    Tabular values of phase function, Legendre polynominal coefficients, 180 deg backscatter, and extinction cross section are given for eight wavelengths in the atmospheric windows between 0.4 and 2.2 microns. Also included are single scattering albedo, asymmetry factor, and refractive indices. These values are based on Mie theory calculations for the standard rediation atmospheres (continental, maritime, urban, unperturbed stratospheric, volcanic, upper atmospheric, soot, oceanic, dust, and water-soluble) assest measured volcanic aerosols at several time intervals following the El Chichon eruption. Comparisons of extinction to 180 deg backscatter for different aerosol models are presented and related to lidar data.

  9. Design Of A Novel Open-Path Aerosol Extinction Cavity Ringdown Spectrometer And Initial Data From Deployment At NOAA's Atmospheric Observatory

    NASA Astrophysics Data System (ADS)

    Gordon, T. D.; Wagner, N. L.; Richardson, M.; Law, D. C.; Wolfe, D. E.; Brock, C. A.; Erdesz, F.; Murphy, D. M.

    2014-12-01

    The ability to frame effective climate change policy depends strongly on reducing the uncertainty in aerosol radiative forcing, which is currently nearly as great as best estimates of its magnitude. Achieving this goal will require significant progress in measuring aerosol properties, including aerosol optical depth, single scattering albedo and the effect of relative humidity on these properties for both fine and coarse particles. However both ground- and space-based instruments fail or are highly biased in the presence of clouds, severely limiting quantitative estimates of the radiative effects of aerosols where they are advected over low-level clouds. Moreover, many in situ aerosol measurements exclude the coarse fraction, which can be very important in and downwind of desert regions. By measuring the decay rate of a pulsed laser in an optically resonant cavity, cavity ringdown spectrometers (CRDSs) have been employed successfully in measuring aerosol extinction for particles in relative humidities below 90%. At very high humidities (as found in and near clouds), however, existing CRDSs perform poorly, diverging significantly from theoretical extinction values as humidities approach 100%. The new open-path aerosol extinction CRDS described in this poster measures extinction as aerosol is drawn through the sample cavity directly without inlets or tubing for channeling the flow, which cause particle losses, condensation at high RH and other artifacts. This poster presents the key elements of the new open-path CRDS design as well as comparisons with an earlier generation closed-path CRDS and preliminary data obtained during a field study at the 300 meter tower at NOAA's Boulder Atmospheric Observatory (BAO) in Colorado.

  10. Aerosol particle absorption spectroscopy by photothermal modulation of Mie scattered light

    SciTech Connect

    Campillo, A.J.; Dodge, C.J.; Lin, H.B.

    1981-09-15

    Absorption spectroscopy of suspended submicron-sized aqueous ammonium-sulfate aerosol droplets has been performed by employing a CO/sub 2/ laser to photothermally modulate visible Mie scattered light. (AIP)

  11. Altitude Differentiated Aerosol Extinction Over Tenerife (North Atlantic Coast) During ACE-2 by Means of Ground and Airborne Photometry and Lidar Measurements

    NASA Technical Reports Server (NTRS)

    Formenti, P.; Elias, T.; Welton, J.; Diaz, J. P.; Exposito, F.; Schmid, B.; Powell, D.; Holben, B. N.; Smirnov, A.; Andreae, M. O.; Devaux, C.; Voss, K.; Lelieveld, J.; Livingston, J. M.; Russell, P. B.; Durkee, P. A.

    2000-01-01

    Retrievals of spectral aerosol optical depths (tau(sub a)) by means of sun photometers have been undertaken in Tenerife (28 deg 16' N, 16 deg 36' W) during ACE-2 (June-July 1997). Five ground-based sites were located at four different altitudes in the marine boundary layer and in the free troposphere, from 0 to 3570 m asl. The goal of the investigation was to provide estimates of the vertical aerosol extinction over the island, both under clean and turbid conditions. Inversion of spectral tau(sub a) allowed to retrieve size distributions, from which the single scattering albedo omega(sub 0) and the asymmetry factor g could be estimated as a function of altitude. These parameters were combined to calculate aerosol forcing in the column. Emphasis is put on episodes of increased turbidity, which were observed at different locations simultaneously, and attributed to outbreaks of mineral dust from North Africa. Differentiation of tau(sub a) as a function of altitude provided the vertical profile of the extinction coefficient sigma(sub e). For dust outbreaks, aerosol extinction is concentrated in two distinct layers above and below the strong subsidence inversion around 1200 m asl. Vertical profiles of tau(sub a) and sigma(sub e) are shown for July 8. In some occasions, vertical profiles are compared to LIDAR observations, performed both at sea level and in the low free troposphere, and to airborne measurements of aerosol optical depths.

  12. Determination of the Aerosol Size Distribution by Analytic Inversion of the Extinction Spectrum in the Complex Anomalous Diffraction Approximation

    NASA Astrophysics Data System (ADS)

    Franssens, Ghislain; de Maziére, Martine; Fonteyn, Dominique

    2000-08-01

    A new derivation is presented for the analytical inversion of aerosol spectral extinction data to size distributions. It is based on the complex analytic extension of the anomalous diffraction approximation (ADA). We derive inverse formulas that are applicable to homogeneous nonabsorbing and absorbing spherical particles. Our method simplifies, generalizes, and unifies a number of results obtained previously in the literature. In particular, we clarify the connection between the ADA transform and the Fourier and Laplace transforms. Also, the effect of the particle refractive-index dispersion on the inversion is examined. It is shown that, when Lorentz s model is used for this dispersion, the continuous ADA inverse transform is mathematically well posed, whereas with a constant refractive index it is ill posed. Further, a condition is given, in terms of Lorentz parameters, for which the continuous inverse operator does not amplify the error.

  13. Changes in surface aerosol extinction trends over China during 1980-2013 inferred from quality-controlled visibility data

    NASA Astrophysics Data System (ADS)

    Li, Jing; Li, Chengcai; Zhao, Chunsheng; Su, Tianning

    2016-08-01

    Pollution in China has been attracting extensive attention both globally and regionally, especially due to the perceptually worsening "smog" condition in recent years. We use routine visibility measurements from 1980 to 2013 at 272 World Meteorological Organization stations in China to assess the temporal changes in the magnitude and the sign of pollution trends. A strict and comprehensive quality control procedure is enforced by considering several issues not typically addressed in previous studies. Two methods are used to independently estimate the trend and its significance level. Results show that, in general, a strong increase in aerosol extinction coefficient over the majority of China is observed in the 1980s, followed by a moderate decrease in the 1990s, another increase in the 2000s, and a shift to decrease since around 2006 for some regions. Seasonally, winter and fall trends appear to be the strongest, while summer has the lowest trend.

  14. Determination of the aerosol size distribution by analytic inversion of the extinction spectrum in the complex anomalous diffraction approximation.

    PubMed

    Franssens, G; De Maziére, M; Fonteyn, D

    2000-08-20

    A new derivation is presented for the analytical inversion of aerosol spectral extinction data to size distributions. It is based on the complex analytic extension of the anomalous diffraction approximation (ADA). We derive inverse formulas that are applicable to homogeneous nonabsorbing and absorbing spherical particles. Our method simplifies, generalizes, and unifies a number of results obtained previously in the literature. In particular, we clarify the connection between the ADA transform and the Fourier and Laplace transforms. Also, the effect of the particle refractive-index dispersion on the inversion is examined. It is shown that, when Lorentz's model is used for this dispersion, the continuous ADA inverse transform is mathematically well posed, whereas with a constant refractive index it is ill posed. Further, a condition is given, in terms of Lorentz parameters, for which the continuous inverse operator does not amplify the error.

  15. Four-year long-path monitoring of ambient aerosol extinction at a central European urban site: dependence on relative humidity

    NASA Astrophysics Data System (ADS)

    Skupin, A.; Ansmann, A.; Engelmann, R.; Seifert, P.; Müller, T.

    2015-04-01

    The ambient aerosol particle extinction coefficient is measured with the Spectral Aerosol Extinction Monitoring System (SÆMS) along a 2.84 km horizontal path at 30-50 m height above ground in the urban environment of Leipzig (51.3° N, 12.4° E), Germany, since 2009. The dependence of the particle extinction coefficient (wavelength range from 300-1000 nm) on relative humidity up to almost 100% was investigated. The main results are presented. For the wavelength of 550 nm, the mean extinction enhancement factor was found to be 1.75 ± 0.4 for an increase of relative humidity from 40 to 80%. The respective four-year mean extinction enhancement factor is 2.8 ± 0.6 for a relative-humidty increase from 40 to 95%. A parameterization of the dependency of the urban particle extinction coefficient on relative humidity is presented. A mean hygroscopic exponent of 0.463 for the 2009-2012 period was determined. Based on a backward trajectory cluster analysis, the dependence of several aerosol optical properties for eight air flow regimes was investigated. Large differences were not found indicating that local pollution sources widely control the aerosol conditions over the urban site. The comparison of the SÆMS extinction coefficient statistics with respective statistics from ambient AERONET sun photometer observations yield good agreement. Also, time series of the particle extinction coefficient computed from in-situ-measured dry particle size distributions and humidity-corrected SÆMS extinction values (for 40% relative humidity) were found in good overall consistency, which corroborates the applicability of the developed humidity parameterization scheme. The analysis of the spectral dependence of particle extinction (Ångström exponent) revealed an increase of the 390-881 nm Ångström exponent from, on average, 0.3 (at 30% relative humidity) to 1.3 (at 95% relative humidity) for the four-year period.

  16. Inter-comparison of MAX-DOAS Retrieved Vertical Profiles of Aerosol Extinction, SO2 and NO2 in the Alberta Oil Sands with LIDAR Data and GEM-MACH Air Quality Model.

    NASA Astrophysics Data System (ADS)

    Davis, Zoe; Friess, Udo; Strawbridge, Kevin; Whiteway, James; Aggarwal, Monika; Makar, Paul; Li, Shao-Meng; O'Brien, Jason; Baray, Sabour; Schnitzler, Elijah; Olfert, Jason S.; Osthoff, Hans D.; Lobo, Akshay; McLaren, Robert

    2016-04-01

    Understanding industrial emissions of trace gas pollutants in the Alberta oil sands is essential to maintaining air quality standards and informing public policy. Multi-Axis Differential Optical Absorption Spectroscopy (MAX-DOAS) measurements of trace gases can improve knowledge of pollutant levels, vertical distribution and chemical transformation. During an intensive air measurement campaign to study emissions, transport, transformation and deposition of oil sands air pollutants from August to September of 2013, a MAX-DOAS instrument was deployed at a site north of Fort McMurray, Alberta to determine the vertical profiles of aerosol extinction, NO2 and SO2 through retrieval from the MAX-DOAS spectral measurements using an optimal estimation method. The large complement of data collected from multiple instruments deployed during this field campaign provides a unique opportunity to validate and characterize the performance of the MAX-DOAS vertical profile retrievals. Aerosol extinction profiles determined from two Light Detection and Ranging (LIDAR) instruments, one collocated and the other on a Twin Otter aircraft that flew over the site during the study, will be compared to the MAX-DOAS aerosol extinction profile retrievals. Vertical profiles of NO2 and SO2 retrieved from the MAX-DOAS measurements will be further compared with the composite vertical profiles measured from the flights of a second aircraft, the NRC-Convair 580, over the field site during the same measurement period. Finally, the MAX-DOAS retrieved tropospheric vertical column densities (VCDs) of SO2 and NO2 will be compared to the predicted VCDs from Environment and Climate Change Canada's Global Environmental Multi-scale - Modelling Air quality and Chemistry (GEM-MACH) air quality model over the grid cell containing the field site. Emission estimates of SO2 from the major oil mining facility Syncrude Mildred Lake using the MAX-DOAS VCD results, validated through the detailed characterization above

  17. Vertical columns of NO2, HONO, HCHO, CHOCHO and aerosol extinction: diurnal and seasonal variations in context of CalNex and CARES

    NASA Astrophysics Data System (ADS)

    Ortega, I.; Coburn, S.; Oetjen, H.; Sinreich, R.; Thalman, R. M.; Waxman, E.; Volkamer, R.

    2011-12-01

    We present results from two ground-based University of Colorado Multi Axis Differential Optical Absorption Spectroscopy (CU-MAX-DOAS) instruments that were deployed during the CALNEX and CARES 2010 field campaigns. Ground based CU-MAX-DOAS measurements were carried out through Dec 2010, and measured vertical column abundances of nitrogen dioxide (NO2), nitrous acid (HONO), formaldehyde (HCHO), glyoxal (CHOCHO), and aerosol extinction, which is determined indirectly from observing the oxygen dimers (O4). The measurements were acquired on the top of Millikan library at Caltech, Pasadena, CA, at the Fontana Arrows site located 60 Km east of Caltech, and for a limited period also downwind of Sacramento at T1 site during CARES. In the South Coast Air Basin, the MAX-DOAS instruments at both sites collected an extended time series of use to test satellites, and atmospheric chemistry models. We determine the state of the planetary boundary layer by comparing the columns observations with in-situ sensors, and place the CALNEX and CARES measurements intensive into seasonal context.

  18. Aerosol Extinction Transmissometry at Visible and Infrared Wavelengths Applied to Specialized Problems in CB Defense

    DTIC Science & Technology

    1989-10-01

    Transmission of Light Through Fog." Phy. hev= 38, 159-165 (1931). 30, Kerker, M., Matijevic . E., Espenscheid. W.F., Farone, W.A., and Kitani, S...W.F., Matijevic , E., and Kerker, M., "Aerosol Studies by Light Scattering. III. Preparation and Particle Size Analysis of Sodium Chloride t.arosols of

  19. Determination of the size distribution of metallic nanoparticles by optical extinction spectroscopy

    SciTech Connect

    Pena, Ovidio; Rodriguez-Fernandez, Luis; Rodriguez-Iglesias, Vladimir; Kellermann, Guinther; Crespo-Sosa, Alejandro; Cheang-Wong, Juan Carlos; Silva-Pereyra, Hector Gabriel; Arenas-Alatorre, Jesus; Oliver, Alicia

    2009-01-20

    A method is proposed to estimate the size distribution of nearly spherical metallic nanoparticles (NPs) from optical extinction spectroscopy (OES) measurements based on Mie's theory and an optimization algorithm. The described method is compared against two of the most widely used techniques for the task: transmission electron microscopy (TEM) and small-angle x-ray scattering (SAXS). The size distribution of Au and Cu NPs, obtained by ion implantation in silica and a subsequent thermal annealing in air, was determined by TEM, grazing-incidence SAXS (GISAXS) geometry, and our method, and the average radius obtained by all the three techniques was almost the same for the two studied metals. Concerning the radius dispersion (RD), OES and GISAXS give very similar results, while TEM considerably underestimates the RD of the distribution.

  20. Quantifying the effect of finite spectral bandwidth on extinction coefficient of species in laser absorption spectroscopy

    NASA Astrophysics Data System (ADS)

    Singh, Manjeet; Singh, Jaswant; Singh, Baljit; Ghanshyam, C.

    2016-11-01

    The aim of this study is to quantify the finite spectral bandwidth effect on laser absorption spectroscopy for a wide-band laser source. Experimental analysis reveals that the extinction coefficient of an analyte is affected by the bandwidth of the spectral source, which may result in the erroneous conclusions. An approximate mathematical model has been developed for optical intensities having Gaussian line shape, which includes the impact of source's spectral bandwidth in the equation for spectroscopic absorption. This is done by introducing a suitable first order and second order bandwidth approximation in the Beer-Lambert law equation for finite bandwidth case. The derived expressions were validated using spectroscopic analysis with higher SBW on a test sample, Rhodamine B. The concentrations calculated using proposed approximation, were in significant agreement with the true values when compared with those calculated with conventional approach.

  1. The vertical distribution of BrO and aerosols in the Arctic: Measurements by active and passive differential optical absorption spectroscopy

    NASA Astrophysics Data System (ADS)

    Frieß, U.; Sihler, H.; Sander, R.; PöHler, D.; Yilmaz, S.; Platt, U.

    2011-07-01

    We present results from multiaxis differential optical absorption spectroscopy (MAX-DOAS) and long-path DOAS (LP-DOAS) measurements performed at the North Slope of Alaska from February to April 2009 as part of the Ocean-Atmosphere-Sea Ice-Snowpack Barrow 2009 campaign. For the first time, vertical profiles of aerosol extinction and BrO in the boundary layer were retrieved simultaneously from MAX-DOAS measurements using the method of optimal estimation. Even at very low visibility, retrieved extinction profiles and aerosol optical thickness are in good agreement with colocated ceilometer and Sun photometer measurements, respectively. BrO surface concentrations measured by MAX-DOAS and LP-DOAS are in very good agreement, and it has been found that useful information on the BrO vertical distribution can be retrieved from MAX-DOAS even in cases when blowing snow strongly reduces visibility. The retrieved BrO and extinction vertical profiles allow for a thorough characterization of the vertical structure of the boundary layer during numerous ozone depletion events observed during Barrow 2009. High BrO concentrations are usually present during the onset of ozone depletion events, and BrO disappears as ozone concentrations approach zero. The finding that elevated BrO concentrations occur mainly in the presence of high extinction near the surface strongly suggests that release of reactive bromine from airborne aerosols and/or ice particles at high wind speed plays an important role. Back trajectory calculations indicate that the particles were transported from the frozen ocean to the measurement site and that the release of reactive bromine from sea ice and/or frost flowers occurs when low temperatures (<250 K) prevail in the regions where reactive bromine is emitted.

  2. Electron mean free path from angle-dependent photoelectron spectroscopy of aerosol particles

    SciTech Connect

    Goldmann, Maximilian; Miguel-Sánchez, Javier; West, Adam H. C.; Yoder, Bruce L.; Signorell, Ruth

    2015-06-14

    We propose angle-resolved photoelectron spectroscopy of aerosol particles as an alternative way to determine the electron mean free path of low energy electrons in solid and liquid materials. The mean free path is obtained from fits of simulated photoemission images to experimental ones over a broad range of different aerosol particle sizes. The principal advantage of the aerosol approach is twofold. First, aerosol photoemission studies can be performed for many different materials, including liquids. Second, the size-dependent anisotropy of the photoelectrons can be exploited in addition to size-dependent changes in their kinetic energy. These finite size effects depend in different ways on the mean free path and thus provide more information on the mean free path than corresponding liquid jet, thin film, or bulk data. The present contribution is a proof of principle employing a simple model for the photoemission of electrons and preliminary experimental data for potassium chloride aerosol particles.

  3. Aerosol particle microphotography and glare-spot absorption spectroscopy.

    PubMed

    Arnold, S; Holler, S; Li, J H; Serpengüzel, A; Auffermann, W F; Hill, S C

    1995-04-01

    The relative intensities of glare spots in the image of an electrodynamically trapped aerosol droplet are measured experimentally with an aerosol particle microscope and calculated theoretically. The theoretical calculations are in good agreement with these experiments and indicate that the intensities of these spots are extremely sensitive to the imaginary part of the refractive index. Experimentally, we obtain the molecular absorption spectrum of an impurity within a droplet by recording the spectrum of an individual glare spot produced by broadband illumination.

  4. Surface-Enhanced Resonance Raman Scattering and Visible Extinction Spectroscopy of Copper Chlorophyllin: An Upper Level Chemistry Experiment

    ERIC Educational Resources Information Center

    Schnitzer, Cheryl S.; Reim, Candace Lawson; Sirois, John J.; House, Paul G.

    2010-01-01

    Advanced chemistry students are introduced to surface-enhanced resonance Raman scattering (SERRS) by studying how sodium copper chlorophyllin (CuChl) adsorbs onto silver colloids (CuChl/Ag) as a function of pH. Using both SERRS and visible extinction spectroscopy, the extent of CuChl adsorption and colloidal aggregation are monitored. Initially at…

  5. Field test of a new instrument to measure UV/Vis (300-700 nm) ambient aerosol extinction spectra in Colorado during DISCOVER-AQ

    NASA Astrophysics Data System (ADS)

    Jordan, C. E.; Anderson, B. E.; Beyersdorf, A. J.; Dibb, J. E.; Greenslade, M. E.; Martin, R.; Scheuer, E. M.; Shook, M.; Thornhill, K. L., II; Troop, D.; Winstead, E.; Ziemba, L. D.

    2014-12-01

    An optical instrument has been developed to investigate aerosol extinction spectra in the ambient atmosphere. Based on a White-type cell design and using a differential optical approach, aerosol extinction spectra over the 300-700 nm ultraviolet and visible (UV/Vis) wavelength range are obtained. Laboratory tests conducted at NASA Langley Research Center (NASA LaRC) in March 2014 showed good agreement with Cavity Attenuated Phase Shift (CAPS PMex, Aerodyne Research) extinction measurements (at 450, 530, and 630 nm) for a variety of aerosols, e.g., scatterers such as polystyrene latex spheres and ammonium sulfate; absorbers such as dust (including pigmented minerals), smoke (generated in a miniCAST burning propane) and laboratory smoke analogs (e.g., fullerene soot and aquadag). The instrument was field tested in Colorado in July and August 2014 aboard the NASA mobile laboratory at various ground sites during the DISCOVER-AQ (Deriving Information on Surface Conditions from Column and Vertically Resolved Observations Relevant to Air Quality) field campaign. A description of the instrument, results from the laboratory tests, and summer field data will be presented. The instrument provides a new tool for probing in situ aerosol optical properties that may help inform remote sensing approaches well into the UV range.

  6. Aerosol optical extinction during the Front Range Air Pollution and Photochemistry Éxperiment (FRAPPÉ) 2014 summertime field campaign, Colorado, USA

    NASA Astrophysics Data System (ADS)

    Dingle, Justin H.; Vu, Kennedy; Bahreini, Roya; Apel, Eric C.; Campos, Teresa L.; Flocke, Frank; Fried, Alan; Herndon, Scott; Hills, Alan J.; Hornbrook, Rebecca S.; Huey, Greg; Kaser, Lisa; Montzka, Denise D.; Nowak, John B.; Reeves, Mike; Richter, Dirk; Roscioli, Joseph R.; Shertz, Stephen; Stell, Meghan; Tanner, David; Tyndall, Geoff; Walega, James; Weibring, Petter; Weinheimer, Andrew

    2016-09-01

    Summertime aerosol optical extinction (βext) was measured in the Colorado Front Range and Denver metropolitan area as part of the Front Range Air Pollution and Photochemistry Éxperiment (FRAPPÉ) campaign during July-August 2014. An Aerodyne cavity attenuated phase shift particle light extinction monitor (CAPS-PMex) was deployed to measure βext (at average relative humidity of 20 ± 7 %) of submicron aerosols at λ = 632 nm at 1 Hz. Data from a suite of gas-phase instrumentation were used to interpret βext behavior in various categories of air masses and sources. Extinction enhancement ratios relative to CO (Δβext / ΔCO) were higher in aged urban air masses compared to fresh air masses by ˜ 50 %. The resulting increase in Δβext / ΔCO for highly aged air masses was accompanied by formation of secondary organic aerosols (SOAs). In addition, the impacts of aerosol composition on βext in air masses under the influence of urban, natural oil and gas operations (O&G), and agriculture and livestock operations were evaluated. Estimated non-refractory mass extinction efficiency (MEE) values for different air mass types ranged from 1.51 to 2.27 m2 g-1, with the minimum and maximum values observed in urban and agriculture-influenced air masses, respectively. The mass distribution for organic, nitrate, and sulfate aerosols presented distinct profiles in different air mass types. During 11-12 August, regional influence of a biomass burning event was observed, increasing the background βext and estimated MEE values in the Front Range.

  7. Aerosol optical properties measurement by recently developed cavity-enhanced aerosol single scattering albedometer

    NASA Astrophysics Data System (ADS)

    Zhao, Weixiong; Xu, Xuezhe; Zhang, Qilei; Fang, Bo; Qian, Xiaodong; Chen, Weidong; Gao, Xiaoming; Zhang, Weijun

    2015-04-01

    Development of appropriate and well-adapted measurement technologies for real-time in-situ measurement of aerosol optical properties is an important step towards a more accurate and quantitative understanding of aerosol impacts on climate and the environment. Aerosol single scattering albedo (SSA, ω), the ratio between the scattering (αscat) and extinction (αext) coefficients, is an important optical parameter that governs the relative strength of the aerosol scattering and absorption capacity. Since the aerosol extinction coefficient is the sum of the absorption and scattering coefficients, a commonly used method for the determination of SSA is to separately measure two of the three optical parameters - absorption, scattering and extinction coefficients - with different instruments. However, as this method involves still different instruments for separate measurements of extinction and absorption coefficients under different sampling conditions, it might cause potential errors in the determination of SSA value, because aerosol optical properties are very sensitive to the sampling conditions such as temperature and relative humidity (RH). In this paper, we report on the development of a cavity-enhanced aerosol single scattering albedometer incorporating incoherent broad-band cavity-enhanced spectroscopy (IBBCEAS) and an integrating sphere (IS) for direct in-situ measurement of aerosol scattering and extinction coefficients on the exact same sample volume. The cavity-enhanced albedometer holds great promise for high-sensitivity and high-precision measurement of ambient aerosol scattering and extinction coefficients (hence absorption coefficient and SSA determination) and for absorbing trace gas concentration. In addition, simultaneous measurements of aerosol scattering and extinction coefficients enable a potential application for the retrieval of particle number size distribution and for faster retrieval of aerosols' complex RI. The albedometer was deployed to

  8. Characterizing the Vertical Profile of Aerosol Particle Extinction and Linear Depolarization over Southeast Asia and the Maritime Continent: The 2007-2009 View from CALIOP

    NASA Technical Reports Server (NTRS)

    Campbell, James R.; Reid, Jeffrey S.; Westphal, Douglas L.; Zhang, Jianglong; Tackett, Jason L.; Chew, Boon Ning; Welton, Ellsworth J.; Shimizu, Atsushi; Sugimoto, Nobuo; Aoki, Kazuma; Winker, David M.

    2012-01-01

    Vertical profiles of 0.532 µm aerosol particle extinction coefficient and linear volume depolarization ratio are described for Southeast Asia and the Maritime Continent. Quality-screened and cloud-cleared Version 3.01 Level 2 NASA Cloud Aerosol Lidar with Orthogonal Polarization (CALIOP) 5-km Aerosol Profile datasets are analyzed from 2007 to 2009. Numerical simulations from the U.S. Naval Aerosol Analysis and Predictive System (NAAPS), featuring two-dimensional variational assimilation of NASA Moderate Resolution Imaging Spectroradiometer and Multi-angle Imaging Spectro- Radiometer quality-assured datasets, combined with regional ground-based lidar measurements, are considered for assessing CALIOP retrieval performance, identifying bias, and evaluating regional representativeness. CALIOP retrievals of aerosol particle extinction coefficient and aerosol optical depth (AOD) are high over land and low over open waters relative to NAAPS (0.412/0.312 over land for all data points inclusive, 0.310/0.235 when the per bin average is used and each is treated as single data points; 0.102/0.151 and 0.086/0.124, respectively, over ocean). Regional means, however, are very similar (0.180/0.193 for all data points and 0.155/0.159 when averaged per normalized bin), as the two factors offset one another. The land/ocean offset is investigated, and discrepancies attributed to interpretation of particle composition and a-priori assignment of the extinction-to-backscatter ratio ("lidar ratio") necessary for retrieving the extinction coefficient from CALIOP signals. Over land, NAAPS indicates more dust present than CALIOP algorithms are identifying, indicating a likely assignment of a higher lidar ratio representative of more absorptive particles. NAAPS resolvesmore smoke overwater than identified with CALIOP, indicating likely usage of a lidar ratio characteristic of less absorptive particles to be applied that biases low AOD there. Over open waters except within the Bay of Bengal

  9. Characterizing the vertical profile of aerosol particle extinction and linear depolarization over Southeast Asia and the Maritime Continent: The 2007-2009 view from CALIOP

    NASA Astrophysics Data System (ADS)

    Campbell, James R.; Reid, Jeffrey S.; Westphal, Douglas L.; Zhang, Jianglong; Tackett, Jason L.; Chew, Boon Ning; Welton, Ellsworth J.; Shimizu, Atsushi; Sugimoto, Nobuo; Aoki, Kazuma; Winker, David M.

    2013-03-01

    Vertical profiles of 0.532 μm aerosol particle extinction coefficient and linear volume depolarization ratio are described for Southeast Asia and the Maritime Continent. Quality-screened and cloud-cleared Version 3.01 Level 2 NASA Cloud Aerosol Lidar with Orthogonal Polarization (CALIOP) 5-km Aerosol Profile datasets are analyzed from 2007 to 2009. Numerical simulations from the U.S. Naval Aerosol Analysis and Predictive System (NAAPS), featuring two-dimensional variational assimilation of NASA Moderate Resolution Imaging Spectroradiometer and Multi-angle Imaging SpectroRadiometer quality-assured datasets, combined with regional ground-based lidar measurements, are considered for assessing CALIOP retrieval performance, identifying bias, and evaluating regional representativeness. CALIOP retrievals of aerosol particle extinction coefficient and aerosol optical depth (AOD) are high over land and low over open waters relative to NAAPS (0.412/0.312 over land for all data points inclusive, 0.310/0.235 when the per bin average is used and each is treated as single data points; 0.102/0.151 and 0.086/0.124, respectively, over ocean). Regional means, however, are very similar (0.180/0.193 for all data points and 0.155/0.159 when averaged per normalized bin), as the two factors offset one another. The land/ocean offset is investigated, and discrepancies attributed to interpretation of particle composition and a-priori assignment of the extinction-to-backscatter ratio (“lidar ratio”) necessary for retrieving the extinction coefficient from CALIOP signals. Over land, NAAPS indicates more dust present than CALIOP algorithms are identifying, indicating a likely assignment of a higher lidar ratio representative of more absorptive particles. NAAPS resolves more smoke over water than identified with CALIOP, indicating likely usage of a lidar ratio characteristic of less absorptive particles to be applied that biases low AOD there. Over open waters except within the Bay of

  10. Mass spectroscopy of single aerosols from field measurements

    SciTech Connect

    Thomson, D.S.; Murphy, D.M.

    1995-12-31

    We are developing an aircraft instrument for the chemical analysis of individual ambient aerosols in real time. In order to test the laboratory version of this instrument, we participated in a field campaign near the continental divide in Colorado in September, 1993. During this campaign, over 5000 mass spectra of ambient aerosols were collected. Analysis of the negative ion spectra shows that sulfate was the most commonly seen component of smaller particles, while nitrate was more common in larger particles. Organic compounds are present in most particles, and we believe we can distinguish inorganic carbon in some particles. Although numerous distinct classes of particles were observed, indicating external mixtures, almost all of these particle types were themselves mixtures of several compounds. Finally, we note that although the field site experienced distinct polluted and unpolluted episodes, aerosol composition did not correlate with gas phase chemistry.

  11. Infrared spectroscopy of sulfuric acid/water aerosols: Freezing characteristics

    NASA Astrophysics Data System (ADS)

    Clapp, M. L.; Niedziela, R. F.; Richwine, L. J.; Dransfield, T.; Miller, R. E.; Worsnop, D. R.

    1997-04-01

    A low-temperature flow cell has been used in conjunction with a Fourier transform infrared (FT-IR) spectrometer to study sulfuric acid/water aerosols. The aerosols were generated with a wide range of composition (28 to 85 wt%), including those characteristic of stratospheric sulfate aerosols, and studied over the temperature range from 240 K to 160 K. The particles exhibited deep supercooling, by as much as 100 K below the freezing point in some cases. Freezing of water ice was observed in the more dilute (<40 wt% sulfuric acid) particles, in agreement with the predictions of Jensen et al. and recent observations by Bertram et al. In contrast with theoretical predictions, however, the entire particle often does not immediately freeze, at least on the timescale of the present experiments (seconds to minutes). Freezing of the entire particle is observed at lower temperatures, well below that characteristic of the polar stratosphere.

  12. MAX-DOAS measurements in southern China: retrieval of aerosol extinctions and validation using ground-based in-situ data

    NASA Astrophysics Data System (ADS)

    Li, X.; Brauers, T.; Shao, M.; Garland, R. M.; Wagner, T.; Deutschmann, T.; Wahner, A.

    2010-03-01

    We performed MAX-DOAS measurements during the PRiDe-PRD2006 campaign in the Pearl River Delta region 50 km north of Guangzhou, China, for 4 weeks in June 2006. We used an instrument sampling at 7 different elevation angles between 3° and 90°. During 9 cloud-free days, differential slant column densities (DSCDs) of O4 (O2 dimer) absorptions between 351 nm and 389 nm were evaluated for 6 elevation angles. Here, we show that radiative transfer modeling of the DSCDS can be used to retrieve the aerosol extinction and the height of the boundary layer. A comparison of the aerosol extinction with simultaneously recorded, ground based nephelometer data shows excellent agreement.

  13. Aerosol Phosphorus Composition: New Insights from Synchrotron X-ray Spectroscopy

    NASA Astrophysics Data System (ADS)

    Longo, A.; Ingall, E. D.; Diaz, J. M.; Oakes, M. M.; King, L.; Nenes, A.; Mihalopoulos, N.; Violaki, K.; Avila, A.; Benitez-Nelson, C. R.; Brandes, J. A.; McNulty, I.; Vine, D.

    2014-12-01

    Biological productivity in many ocean regions is controlled by the availability of the nutrient phosphorus (P), including the eastern Mediterranean Sea. Aerosol deposition is a key source of P in the Mediterranean. Understanding the composition of this P is critical for determining its solubility and therefore potential bioavailability. We investigated aerosol P composition in European and North African air masses, the main sources of aerosol deposition to the Mediterranean Sea, using Phosphorus Near Edge X-ray Fluorescence Spectroscopy (P-NEXFS). We show that European aerosols are a significant source of soluble P to the Mediterranean Sea. The traditionally studied North African sourced air masses carry more total P to the Mediterranean Sea than European sourced air masses and contain mostly apatite, a largely insoluble calcium phosphate mineral. However, European aerosols deliver P that is on average 3.5 times more soluble than North African aerosols and furthermore are dominated by organic P compounds. The increased solubility of European aerosols leads to comparable amounts of soluble P by mass delivered to the Mediterranean Sea by both air masses. The ultimate origin of organic P does not stem from common primary emission sources, such as coal fly ash and diesel emissions. Rather, P associated with bacteria best explains the presence of organic P in Mediterranean aerosols. The soluble organic nature of the P in European sourced air masses underscores the need to examine aerosols from this region as a source of P to the Mediterranean Sea. This study also demonstrates that synchrotron-based techniques are effective tools for characterizing aerosols and gaining new insights.

  14. Use of In Situ Cloud Condensation Nuclei, Extinction, and Aerosol Size Distribution Measurements to Test a Method for Retrieving Cloud Condensation Nuclei Profiles From Surface Measurements

    NASA Technical Reports Server (NTRS)

    Ghan, Stephen J.; Rissman, Tracey A.; Ellman, Robert; Ferrare, Richard A.; Turner, David; Flynn, Connor; Wang, Jian; Ogren, John; Hudson, James; Jonsson, Haflidi H.; VanReken, Timothy; Flagan, Richard C.; Seinfeld, John H.

    2006-01-01

    If the aerosol composition and size distribution below cloud are uniform, the vertical profile of cloud condensation nuclei (CCN) concentration can be retrieved entirely from surface measurements of CCN concentration and particle humidification function and surface-based retrievals of relative humidity and aerosol extinction or backscatter. This provides the potential for long-term measurements of CCN concentrations near cloud base. We have used a combination of aircraft, surface in situ, and surface remote sensing measurements to test various aspects of the retrieval scheme. Our analysis leads us to the following conclusions. The retrieval works better for supersaturations of 0.1% than for 1% because CCN concentrations at 0.1% are controlled by the same particles that control extinction and backscatter. If in situ measurements of extinction are used, the retrieval explains a majority of the CCN variance at high supersaturation for at least two and perhaps five of the eight flights examined. The retrieval of the vertical profile of the humidification factor is not the major limitation of the CCN retrieval scheme. Vertical structure in the aerosol size distribution and composition is the dominant source of error in the CCN retrieval, but this vertical structure is difficult to measure from remote sensing at visible wavelengths.

  15. 1984-1995 Evolution of Stratospheric Aerosol Size, Surface Area, and Volume Derived by Combining SAGE II and CLAES Extinction Measurements

    NASA Technical Reports Server (NTRS)

    Russell, Philip B.; Bauman, Jill J.

    2000-01-01

    This SAGE II Science Team task focuses on the development of a multi-wavelength, multi- sensor Look-Up-Table (LUT) algorithm for retrieving information about stratospheric aerosols from global satellite-based observations of particulate extinction. The LUT algorithm combines the 4-wavelength SAGE II extinction measurements (0.385 <= lambda <= 1.02 microns) with the 7.96 micron and 12.82 micron extinction measurements from the Cryogenic Limb Array Etalon Spectrometer (CLAES) instrument, thus increasing the information content available from either sensor alone. The algorithm uses the SAGE II/CLAES composite spectra in month-latitude-altitude bins to retrieve values and uncertainties of particle effective radius R(sub eff), surface area S, volume V and size distribution width sigma(sub g).

  16. Analysis of Venus Express optical extinction due to aerosols in the upper haze of Venus

    NASA Astrophysics Data System (ADS)

    Parkinson, Christopher; Bougher, Stephen; Mahieux, Arnaud; Tellmann, Silvia; Pätzold, Martin; Vandaele, Ann C.; Wilquet, Valérie; Schulte, Rick; Yung, Yuk; Gao, Peter; Bardeen, Charles

    Observations by the SPICAV/SOIR instruments aboard Venus Express (VEx) have revealed that the Upper Haze of Venus is populated by two particle modes, as reported by Wilquet et al. (J. Geophys. Res., 114, E00B42, 2009; Icarus 217, 2012). Gao et al. (In press, Icarus, 2013) posit that the large mode is made up of cloud particles that have diffused upwards from the cloud deck below, while the smaller mode is generated by the in situ nucleation of meteoric dust. They tested this hypothesis by using version 3.0 of the Community Aerosol and Radiation Model for Atmospheres, first developed by Turco et al. (J. Atmos. Sci., 36, 699-717, 1979) and upgraded to version 3.0 by Bardeen et al. (The CARMA 3.0 microphysics package in CESM, Whole Atmosphere Working Group Meeting, 2011). Using the meteoric dust production profile of Kalashnikova et al. (Geophys. Res. Lett., 27, 3293-3296, 2000), the sulfur/sulfate condensation nuclei production profile of Imamura and Hashimoto (J. Atmos. Sci., 58, 3597-3612, 2001), and sulfuric acid vapor production profile of Zhang et al. (Icarus, 217, 714-739, 2012), they numerically simulate a column of the Venus atmosphere from 40 to 100 km above the surface. Their aerosol number density results agree well with Pioneer Venus Orbiter (PVO) data from Knollenberg and Hunten (J. Geophys. Res., 85, 8039-8058, 1980), while their gas distribution results match that of Kolodner and Steffes below 55 km (Icarus, 132, 151-169, 1998). The resulting size distribution of cloud particles shows two distinct modes, qualitatively matching the observations of PVO. They also observe a third mode in their results with a size of a few microns at 48 km altitude, which appears to support the existence of the controversial third mode in the PVO data. This mode disappears if coagulation is not included in the simulation. The Upper Haze size distribution shows two lognormal-like distributions overlapping each other, possibly indicating the presence of the two distinct

  17. Aerosol Optical Extinction during the Front Range Air Pollution and Photochemistry Experiment (FRAPPE) 2014 Summertime Field Campaign, Colorado U.S.A.

    NASA Astrophysics Data System (ADS)

    Dingle, J. H.; Vu, K. K. T.; Bahreini, R.; Apel, E. C.; Campos, T. L.; Cantrell, C. A.; Cohen, R. C.; Ebben, C. J.; Flocke, F. M.; Fried, A.; Herndon, S. C.; Hills, A. J.; Hornbrook, R. S.; Huey, L. G.; Kaser, L.; Mauldin, L.; Montzka, D. D.; Nowak, J. B.; Richter, D.; Roscioli, J. R.; Shertz, S.; Stell, M. H.; Tanner, D.; Tyndall, G. S.; Walega, J.; Weibring, P.; Weinheimer, A. J.

    2015-12-01

    Aerosol optical extinction (βext) was measured in the Colorado Front Range Denver Metropolitan Area as part of the summertime air quality airborne field campaign to characterize the influence of sources, photochemical processing, and transport of pollution on local air quality. An Aerodyne Cavity Attenuated Phase Shift particle light extinction monitor (CAPS-PMex) was deployed to measure dry βext at λ=632 nm at 1 Hz. Data from a suite of gas-phase instrumentation were used to interpret the βext under various categories of aged air masses and sources. Extinction enhancement ratios of Δβext/ΔCO were evaluated under 3 differently aged air mass categories (fresh, intermediately aged, and aged) to investigate impacts of photochemistry on βext. Δβext/ΔCO was significantly increased in heavily aged air masses compared to fresh air masses (0.17 Mm-1/ppbv and 0.094 Mm-1/ppbv respectively). The resulting increase in Δβext/ΔCO under heavily aged air masses was represented by secondary organic aerosols (SOA) formation. Aerosol composition and sources from urban, natural oil and gas wells (OG), and agriculture and livestock operations were also evaluated for their impacts on βext. Linear regression fits to βext vs. organic aerosol mass showed higher correlation coefficients under the urban and OG plumes (r=0.55 and r=0.71 respectively) and weakest under agricultural and livestock plumes (r=0.28). The correlation between βext and nitrate aerosol mass however was best under the agriculture and livestock plumes (r=0.81), followed by OG plumes (r=0.74), suggesting co-location of aerosol nitrate precursor sources with OG emissions. Finally, non-refractory mass extinction efficiency (MEE) was analyzed. MEE was observed to be 1.37 g/m2 and 1.30 g/m2 in OG and urban+OG plumes, respectively.

  18. Analysis of Venus Express optical extinction due to aerosols in the upper haze of Venus

    NASA Astrophysics Data System (ADS)

    Parkinson, C. D.; Bougher, S. W.; Schulte, R.; Gao, P.; Yung, Y. L.; Vandaele, A.; Wilquet, V.; Mahieux, A.; Tellmann, S.

    2013-12-01

    Observations by the SPICAV/SOIR instruments aboard the Venus Express (VEx) spacecraft have revealed that the upper haze (UH) of Venus, between 70 and 90 km, is variable on the order of days to weeks and that it is populated by two particle modes. Gao et al. (submitted, Icarus, 2013) posit that one mode is made up of cloud particles that have diffused upwards from the main sulfuric acid cloud deck below, while the other mode is generated in situ by nucleation of sulfuric acid droplets on meteoric dust. They also propose that the observed variability in the UH is caused in part by vertical transient winds. They test this hypothesis by simulating a column of the Venus atmosphere from 40 to 100 km above the surface using a model based upon the Community Aerosol and Radiation Model for Atmospheres (CARMA). In this work, we significantly extend the analysis using the new more detailed SOIR/VeRa VEx temperature profiles which better constrain the observed strong CO2 15-micron cooling emission and 4.3-μm near-IR heating in Venus' atmosphere (and consistent with Venus Thermospheric General Circulation Model (VTGCM) simulations of Brecht et al. (2011)). We discuss our new results in context of the recent VEx observations (Wilquet et al., Icarus 217, 2012) with an intercomparison with the PVO data. We will also discuss similarities and differences arising from the PVO and VEx epochs where they exist. Additionally we report on our efforts self-consistently applying the VTGCM to constrain the degree to which effects due to vertical transient wind simulations can establish variability timescales and number density profiles that match VEx observations.

  19. Infrared spectroscopy and Mie scattering of acetylene aerosols formed in a low temperature diffusion cell

    NASA Technical Reports Server (NTRS)

    Dunder, T.; Miller, R. E.

    1990-01-01

    A method is described for forming and spectroscopically characterizing cryogenic aerosols formed in a low temperature gas cell. By adjusting the cell pressure, gas composition and flow rate, the size distribution of aerosol particles can be varied over a wide range. The combination of pressure and flow rate determine the residence time of the aerosols in the cell and hence the time available for the particles to grow. FTIR spectroscopy, over the range from 600/cm to 6000/cm, is used to characterize the aerosols. The particle size distribution can be varied so that, at one extreme, the spectra show only absorption features associated with the infrared active vibrational bands and, at the other, they display both absorption and Mie scattering. In the latter case, Mie scattering theory is used to obtain semiquantitative aerosol size distributions, which can be understood in terms of the interplay between nucleation and condensation. In the case of acetylene aerosols, the infrared spectra suggest that the particles exist in the high temperature cubic phase of the solid.

  20. Use of Cavity Ring Down Spectroscopy to Characterize Organic Acids and Aerosols Emitted in Biomass Burning

    NASA Astrophysics Data System (ADS)

    Bililign, Solomon; Fiddler, Marc; Singh, Sujeeta

    2012-02-01

    One poorly understood, but significant class of volatile organic compounds (VOC) present in biomass burning is gas-phase organic acids and inorganic acids. These acids are extremely difficult to measure because of their adsorptive nature. Particulates and aerosols are also produced during biomass burning and impact the radiation budget of the Earth and, hence, impact global climate. Use cavity ring down spectroscopy (CRD) to measure absorption cross sections for OH overtone induced photochemistry in some organic acids (acetic acid and peracetic acid) will be presented and planed measurements of optical properties of aerosols composed of mixtures of different absorbing and non-absorbing species using CRD will be discussed.

  1. A rapid method to derive horizontal distributions of trace gases and aerosols near the surface using multi-axis differential optical absorption spectroscopy

    NASA Astrophysics Data System (ADS)

    Wang, Y.; Li, A.; Xie, P. H.; Wagner, T.; Chen, H.; Liu, W. Q.; Liu, J. G.

    2014-06-01

    We apply a novel experimental procedure for the rapid measurement of the average volume mixing ratios (VMRs) and horizontal distributions of trace gases such as NO2, SO2, and HCHO in the boundary layer, which was recently suggested by Sinreich et al. (2013). The method is based on two-dimensional scanning multi-axis differential optical absorption spectroscopy (MAX-DOAS). It makes use of two facts (Sinreich et al., 2013): first, the light path for observations at 1° elevation angle traverses mainly air masses located close to the ground (typically < 200 m); second, the light path length can be calculated using the simultaneous measured absorption of the oxygen dimer O4. Thus, the average value of the trace gas VMR in the atmospheric layer between the surface and the particular altitude, for which this observation was sensitive, can be calculated. Compared to the originally proposed method, we introduce several important modifications and improvements: We apply the method only to measurements at 1° elevation angle (besides zenith view), for which the uncertainties of the retrieved values of the VMRs and surface extinctions are especially small. Using only 1° elevation angle for off-axis observation also allows an increased temporal resolution. We determine (and apply) correction factors (and their uncertainties) directly as function of the measured O4 absorption. Finally, the method is extended to trace gases analysed at other wavelengths and also to the retrieval of aerosol extinction. Depending on atmospheric visibility, the typical uncertainty of the results ranges from about 20% to 30%. We apply the rapid method to observations of a newly-developed ground-based multifunctional passive differential optical absorption spectroscopy (GM-DOAS) instrument in the north-west outskirts near Hefei in China. We report NO2, SO2, and HCHO VMRs and aerosol extinction for four azimuth angles and compare these results with those from simultaneous long-path DOAS observations

  2. Variation of haemoglobin extinction coefficients can cause errors in the determination of haemoglobin concentration measured by near-infrared spectroscopy

    NASA Astrophysics Data System (ADS)

    Kim, J. G.; Liu, H.

    2007-10-01

    Near-infrared spectroscopy or imaging has been extensively applied to various biomedical applications since it can detect the concentrations of oxyhaemoglobin (HbO2), deoxyhaemoglobin (Hb) and total haemoglobin (Hbtotal) from deep tissues. To quantify concentrations of these haemoglobin derivatives, the extinction coefficient values of HbO2 and Hb have to be employed. However, it was not well recognized among researchers that small differences in extinction coefficients could cause significant errors in quantifying the concentrations of haemoglobin derivatives. In this study, we derived equations to estimate errors of haemoglobin derivatives caused by the variation of haemoglobin extinction coefficients. To prove our error analysis, we performed experiments using liquid-tissue phantoms containing 1% Intralipid in a phosphate-buffered saline solution. The gas intervention of pure oxygen was given in the solution to examine the oxygenation changes in the phantom, and 3 mL of human blood was added twice to show the changes in [Hbtotal]. The error calculation has shown that even a small variation (0.01 cm-1 mM-1) in extinction coefficients can produce appreciable relative errors in quantification of Δ[HbO2], Δ[Hb] and Δ[Hbtotal]. We have also observed that the error of Δ[Hbtotal] is not always larger than those of Δ[HbO2] and Δ[Hb]. This study concludes that we need to be aware of any variation in haemoglobin extinction coefficients, which could result from changes in temperature, and to utilize corresponding animal's haemoglobin extinction coefficients for the animal experiments, in order to obtain more accurate values of Δ[HbO2], Δ[Hb] and Δ[Hbtotal] from in vivo tissue measurements.

  3. Optical and physical properties of stratospheric aerosols from balloon measurements in the visible and near-infrared domains. II. Comparison of extinction, reflectance, polarization, and counting measurements

    NASA Astrophysics Data System (ADS)

    Renard, Jean-Baptiste; Berthet, Gwenaël; Robert, Claude; Chartier, Michel; Pirre, Michel; Brogniez, Colette; Herman, Maurice; Verwaerde, Christian; Balois, Jean-Yves; Ovarlez, Joëlle; Ovarlez, Henri; Crespin, Jacques; Deshler, Terry

    2002-12-01

    The physical properties of stratospheric aerosols can be retrieved from optical measurements involving extinction, radiance, polarization, and counting. We present here the results of measurements from the balloonborne instruments AMON, SALOMON, and RADIBAL, and from the French Laboratoire de Météorologie Dynamique and the University of Wyoming balloonborne particle counters. A cross comparison of the measurements was made for observations of background aerosols conducted during the polar winters of February 1997 and January-February 2000 for various altitudes from 13 to 19 km. On the one hand, the effective radius and the total amount of background aerosols derived from the various sets of data are similar and are in agreement with pre-Pinatubo values. On the other hand, strong discrepancies occur in the shapes of the bimodal size distributions obtained from analysis of the raw measurements of the various instruments. It seems then that the log-normal assumption cannot fully reproduce the size distribution of background aerosols. The effect of the presence of particular aerosols on the measurements is discussed, and a new strategy for observations is proposed.

  4. 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.

  5. A Chronology of Annual-Mean Effective Radii of Stratospheric Aerosols from Volcanic Eruptions During the Twentieth Century as Derived From Ground-based Spectral Extinction Measurements

    NASA Technical Reports Server (NTRS)

    Strothers, Richard B.; Hansen, James E. (Technical Monitor)

    2001-01-01

    Stratospheric extinction can be derived from ground-based spectral photometric observations of the Sun and other stars (as well as from satellite and aircraft measurements, available since 1979), and is found to increase after large volcanic eruptions. This increased extinction shows a characteristic wavelength dependence that gives information about the chemical composition and the effective (or area weighted mean) radius of the particles responsible for it. Known to be tiny aerosols constituted of sulfuric acid in a water solution, the stratospheric particles at midlatitudes exhibit a remarkable uniformity of their column-averaged effective radii r(sub eff) in the first few months after the eruption. Considering the seven largest eruptions of the twentieth century, r(sub eff) at this phase of peak aerosol abundance is approx. 0.3 micrometers in all cases. A year later, r(sub eff) either has remained about the same size (almost certainly in the case of the Katmai eruption of 1912) or has increased to approx. 0.5 micrometers (definitely so for the Pinatubo eruption of 1991). The reasons for this divergence in aerosol growth are unknown.

  6. Characteristics of solid aerosols produced by optical catapulting studied by laser-induced breakdown spectroscopy

    NASA Astrophysics Data System (ADS)

    Fortes, F. J.; Laserna, J. J.

    2010-08-01

    Optical catapulting (OC) constitutes an effective method to transport small amounts of different materials in the form of a solid aerosol. In this report, laser-induced breakdown spectroscopy (LIBS) is used for the analysis of those aerosols produced by OC. For this purpose, materials were catapulted using a Q-switch Nd:YAG laser. A second Q-switch Nd:YAG laser was used for LIBS analysis of the ejected particles. Data processing of aerosols was conducted using conditional data analysis. Also, the standard deviation method was used for the qualitative identification of the ejected particles. Two modes of interaction in OC (OC with focused or defocused pulses) have been evaluated and discussed. LIBS demonstrates that the distribution (spreading) of the ejected particles along the propagation axis increased as a function of the interpulse delay time. The mass density and the thickness of the target also play an important role in OC-LIBS.

  7. Nuclear magnetic resonance spectroscopy for determining the functional content of organic aerosols: a review.

    PubMed

    Chalbot, Marie-Cecile G; Kavouras, Ilias G

    2014-08-01

    The knowledge deficit of organic aerosol (OA) composition has been identified as the most important factor limiting our understanding of the atmospheric fate and implications of aerosol. The efforts to chemically characterize OA include the increasing utilization of nuclear magnetic resonance spectroscopy (NMR). Since 1998, the functional composition of different types, sizes and fractions of OA has been studied with one-dimensional, two-dimensional and solid state proton and carbon-13 NMR. This led to the use of functional group ratios to reconcile the most important sources of OA, including secondary organic aerosol and initial source apportionment using positive matrix factorization. Future research efforts may be directed towards the optimization of experimental parameters, detailed NMR experiments and analysis by pattern recognition methods to identify the chemical components, determination of the NMR fingerprints of OA sources and solid state NMR to study the content of OA as a whole.

  8. 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 ...

  9. 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.

  10. Simultaneous ion luminescence imaging and spectroscopy of individual aerosol particles with external proton or helium microbeams

    NASA Astrophysics Data System (ADS)

    Kada, Wataru; Satoh, Takahiro; Yokoyama, Akihito; Koka, Masashi; Kamiya, Tomihiro

    2014-08-01

    Simultaneous microscopic imaging and spectroscopy of individual aerosol particles were performed with an external microbeam. Visible luminescence induced by the external microbeam was successfully used as a probe to detect organic contaminants in the targets. Combined ion luminescence (IL)/particle-induced X-ray emission (PIXE) analysis of the aerosol targets revealed microscopic chemical and elemental composition distributions under ambient atmospheric conditions. The simple confocal micro-optics for the IL spectroscopy and microscopic imaging were sufficiently sensitive for detecting these molecules at sub-parts per million concentrations and at a wavelength resolution of less than 5 nm. The IL spectra were monitored to prevent severe damage to the samples. Furthermore, our IL system has the advantage that it is simple to add to a conventional micro-PIXE system.

  11. Method and apparatus for aerosol particle absorption spectroscopy

    DOEpatents

    Campillo, Anthony J.; Lin, Horn-Bond

    1983-11-15

    A method and apparatus for determining the absorption spectra, and other properties, of aerosol particles. A heating beam source provides a beam of electromagnetic energy which is scanned through the region of the spectrum which is of interest. Particles exposed to the heating beam which have absorption bands within the band width of the heating beam absorb energy from the beam. The particles are also illuminated by light of a wave length such that the light is scattered by the particles. The absorption spectra of the particles can thus be determined from an analysis of the scattered light since the absorption of energy by the particles will affect the way the light is scattered. Preferably the heating beam is modulated to simplify the analysis of the scattered light. In one embodiment the heating beam is intensity modulated so that the scattered light will also be intensity modulated when the particles absorb energy. In another embodiment the heating beam passes through an interferometer and the scattered light reflects the Fourier Transform of the absorption spectra.

  12. Determination of the biogenic secondary organic aerosol fraction in the boreal forest by NMR spectroscopy

    NASA Astrophysics Data System (ADS)

    Finessi, E.; Decesari, S.; Paglione, M.; Giulianelli, L.; Carbone, C.; Gilardoni, S.; Fuzzi, S.; Saarikoski, S.; Raatikainen, T.; Hillamo, R.; Allan, J.; Mentel, Th. F.; Tiitta, P.; Laaksonen, A.; Petäjä, T.; Kulmala, M.; Worsnop, D. R.; Facchini, M. C.

    2012-01-01

    The study investigates the sources of fine organic aerosol (OA) in the boreal forest, based on measurements including both filter sampling (PM1) and online methods and carried out during a one-month campaign held in Hyytiälä, Finland, in spring 2007. Two aerosol mass spectrometers (Q-AMS, ToF-AMS) were employed to measure on-line concentrations of major non-refractory aerosol species, while the water extracts of the filter samples were analyzed by nuclear magnetic resonance (NMR) spectroscopy for organic functional group characterization of the polar organic fraction of the aerosol. AMS and NMR spectra were processed separately by non-negative factorization algorithms, in order to apportion the main components underlying the submicrometer organic aerosol composition and depict them in terms of both mass fragmentation patterns and functional group compositions. The NMR results supported the AMS speciation of oxidized organic aerosol (OOA) into two main fractions, which could be generally labelled as more and less oxidized organics. The more oxidized component was characterized by a mass spectrum dominated by the m/z 44 peak, and in parallel by a NMR spectrum showing aromatic and aliphatic backbones highly substituted with oxygenated functional groups (carbonyls/carboxyls and hydroxyls). Such component, contributing on average 50% of the OA mass throughout the observing period, was associated with pollution outbreaks from the Central Europe. The less oxidized component was enhanced in concomitance with air masses originating from the North-to-West sector, in agreement with previous investigations conducted at this site. NMR factor analysis was able to separate two distinct components under the less oxidized fraction of OA. One of these NMR-factors was associated with the formation of terrestrial biogenic secondary organic aerosol (BSOA), based on the comparison with spectral profiles obtained from laboratory experiments of terpenes photo-oxidation. The second NMR

  13. A rapid method to derive horizontal distributions of trace gases and aerosols near the surface using multi-axis differential optical absorption spectroscopy

    NASA Astrophysics Data System (ADS)

    Wang, Y.; Li, A.; Xie, P. H.; Wagner, T.; Chen, H.; Liu, W. Q.; Liu, J. G.

    2013-09-01

    We apply a novel experimental procedure for the rapid measurement of the average volume mixing ratios (VMRs) and horizontal distributions of trace gases such as NO2, SO2, and HCHO in the boundary layer, which was recently suggested by Sinreich et al. (2013). The method is based on two-dimensional scanning multi-axis differential optical absorption spectroscopy (MAX-DOAS). It makes use of two facts (Sinreich et al. 2013): First, the light path for observations at 1° elevation angle traverses mainly air masses located close to the ground (typically < 200 m). Second, the light path length can be calculated using the simultaneous measured absorption of the oxygen dimer O4. Thus, the average value of the trace gas VMR in the atmospheric layer between the surface and the altitude, for which this observation was sensitive, can be calculated. Compared to the originally proposed method, we introduce several important modifications and improvements: We apply the method only to measurements at 1° elevation angles, for which the uncertainties are especially small. Using only 1 elevation angle also allows an increased temporal resolution. We apply correction factors (and their uncertainties) as function of the simultaneously modelled O4 absorption. In this way the correction factors can be directly determined according to the measured O4 dAMF. Finally, the method is extended to trace gases analysed at other wavelengths and also to the retrieval of the aerosol extinction. Depending on the atmospheric visibility, the typical uncertainty of the results ranges from about 15 to 30%. We apply the rapid method to observations of a newly developed ground-based multifunctional passive differential optical absorption spectroscopy (GM-DOAS) instrument in the north-west outskirt near Hefei City in China. We report NO2, SO2, and HCHO VMRs and aerosol extinction for four azimuth angles and compare these results with those from simultaneous long-path DOAS observations. Good agreement is

  14. Toward new techniques to measure heterogeneous oxidation of aerosol: Electrodynamic Balance-Mass Spectrometry (EDB-MS) and Aerosol X-ray Photoelectron Spectroscopy

    NASA Astrophysics Data System (ADS)

    Jacobs, M. I.; Heine, N.; Xu, B.; Davies, J. F.; Kirk, B. B.; Kostko, O.; Alayoglu, S.; Wilson, K. R.; Ahmed, M.

    2015-12-01

    The chemical composition and physical properties of aerosol can be changed via heterogeneous oxidation with the OH radical. However, the physical state of the aerosol influences the kinetics of this reaction; liquid particles with a high diffusion coefficient are expected to be well mixed and homogenously oxidized, while oxidation of solid, diffusion-limited aerosol is expected to occur primarily on the surface, creating steep chemical gradients within the particle. We are working to develop several new techniques to study the heterogeneous oxidation of different types of aerosol. We are developing a "modular" electrodynamic balance (EDB) that will enable us to study heterogeneous oxidation at aqueous interfaces using a mass-spectrometer (and potentially other detection techniques). Using a direct analysis in real time (DART) interface, preliminary droplet train measurements have demonstrated single-droplet mass spectrometry to be possible. With long reaction times in our EDB, we will be able to study heterogeneous oxidation of a wide variety of organic species in aqueous droplets. Additionally, we are working to use aerosol photoemission and velocity map imaging (VMI) to study the surface of aerosol particles as they undergo heterogeneous oxidation. With VMI, we're able to collect electrons with a 4π collection efficiency over conventional electron energy analyzers. Preliminary results looking at the ozonolysis of squalene using ultraviolet photoelectron spectroscopy (UPS) show that heterogeneous oxidation kinetic data can be extracted from photoelectron spectra. By moving to X-ray photoemission spectroscopy (XPS), we will determine elemental and chemical composition of the aerosol surface. Thus, aerosol XPS will provide information on the steep chemical gradients that form as diffusion-limited aerosol undergo heterogeneous oxidation.

  15. Three-dimensional dust aerosol distribution and extinction climatology over northern Africa simulated with the ALADIN numerical prediction model from 2006 to 2010

    NASA Astrophysics Data System (ADS)

    Mokhtari, M.; Tulet, P.; Fischer, C.; Bouteloup, Y.; Bouyssel, F.; Brachemi, O.

    2015-08-01

    The seasonal cycle and optical properties of mineral dust aerosols in northern Africa were simulated for the period from 2006 to 2010 using the numerical atmospheric model ALADIN (Aire Limitée Adaptation dynamique Développement InterNational) coupled to the surface scheme SURFEX (SURFace EXternalisée). The particularity of the simulations is that the major physical processes responsible for dust emission and transport, as well as radiative effects, are taken into account on short timescales and at mesoscale resolution. The aim of these simulations is to quantify the dust emission and deposition, locate the major areas of dust emission and establish a climatology of aerosol optical properties in northern Africa. The mean monthly aerosol optical thickness (AOT) simulated by ALADIN is compared with the AOTs derived from the standard Dark Target (DT) and Deep Blue (DB) algorithms of the Aqua-MODIS (MODerate resolution Imaging Spectroradiometer) products over northern Africa and with a set of sun photometer measurements located at Banizoumbou, Cinzana, Soroa, Mbour and Cape Verde. The vertical distribution of dust aerosol represented by extinction profiles is also analysed using CALIOP (Cloud-Aerosol Lidar with Orthogonal Polarization) observations. The annual dust emission simulated by ALADIN over northern Africa is 878 Tg year-1. The Bodélé Depression appears to be the main area of dust emission in northern Africa, with an average estimate of about 21.6 Tg year-1. The simulated AOTs are in good agreement with satellite and sun photometer observations. The positions of the maxima of the modelled AOTs over northern Africa match the observed positions, and the ALADIN simulations satisfactorily reproduce the various dust events over the 2006-2010 period. The AOT climatology proposed in this paper provides a solid database of optical properties and consolidates the existing climatology over this region derived from satellites, the AERONET network and regional climate

  16. Raman Lidar Measurements of Aerosol Extinction and Backscattering. Report 2; Derivation of Aerosol Real Refractive Index, Single-Scattering Albedo, and Humidification Factor using Raman Lidar and Aircraft Size Distribution

    NASA Technical Reports Server (NTRS)

    Ferrare, R. A.; Melfi, S. H.; Whiteman, D. N.; Evans, K. D.; Poellot, M.; Kaufman, Y. J.

    1998-01-01

    Aerosol backscattering and extinction profiles measured by the NASA Goddard Space Flight Center Scanning Raman Lidar (SRL) during the remote cloud sensing (RCS) intensive operations period (IOP) at the Department of Energy Atmospheric Radiation Measurement (ARM) southern Great Plains (SGP) site during two nights in April 1994 are discussed. These profiles are shown to be consistent with the simultaneous aerosol size distribution measurements made by a PCASP (Passive Cavity Aerosol Spectrometer Probe) optical particle counter flown on the University of North Dakota Citation aircraft. We describe a technique which uses both lidar and PCASP measurements to derive the dependence of particle size on relative humidity, the aerosol real refractive index n, and estimate the effective single-scattering albedo Omega(sub 0). Values of n ranged between 1.4-1.5 (dry) and 1.37-1.47 (wet); Omega(sub 0) varied between 0.7 and 1.0. The single-scattering albedo derived from this technique is sensitive to the manner in which absorbing particles are represented in the aerosol mixture; representing the absorbing particles as an internal mixture rather than the external mixture assumed here results in generally higher values of Omega(sub 0). The lidar measurements indicate that the change in particle size with relative humidity as measured by the PCASP can be represented in the form discussed by Hattel with the exponent gamma = 0.3 + or - 0.05. The variations in aerosol optical and physical characteristics captured in the lidar and aircraft size distribution measurements are discussed in the context of the meteorological conditions observed during the experiment.

  17. Relationships between aerosol optical depth and surface-layer extinction in the central part of the Upper Silesia industrial region over the period of 1983-1994

    NASA Astrophysics Data System (ADS)

    Sztyler, Apoloniusz

    The subject of analysis is the aerosol optical depth (AOD) in the visible part of the solar spectrum (τ) (wavelength λ=0.295-0.695μ m). Calculation of τ-values was based on pyrheliometric observation data performed from 1983 to 1994 at IEIA's station (Katowice-Załęże). This paper examines the dependence of τ and its relation to surface-layer extinction coefficient σ (Koschmider quotient of 3.912 and visibility V) on meteorological and anthropological factors during the observation period. Knowledge of the relationship between columnar aerosol turbidity (which can be expressed by τ) and σ allows a more precise and accurate estimation of the aerosol effect on the radiative composition of climate. This work offers some contributions to solving this problem. Therefore, the relations have been described in the form of mathematical/statistical models of AOD (based on "momentary" and mean seasonal values), in which meteorological (and astronomical) parameters as well as the amount of industry dust emission were used as independent variables to improve exactness and credibility in the models.

  18. High-extinction virtually imaged phased array-based Brillouin spectroscopy of turbid biological media.

    PubMed

    Fiore, Antonio; Zhang, Jitao; Shao, Peng; Yun, Seok Hyun; Scarcelli, Giuliano

    2016-05-16

    Brillouin microscopy has recently emerged as a powerful technique to characterize the mechanical properties of biological tissue, cell, and biomaterials. However, the potential of Brillouin microscopy is currently limited to transparent samples, because Brillouin spectrometers do not have sufficient spectral extinction to reject the predominant non-Brillouin scattered light of turbid media. To overcome this issue, we combined a multi-pass Fabry-Perot interferometer with a two-stage virtually imaged phased array spectrometer. The Fabry-Perot etalon acts as an ultra-narrow band-pass filter for Brillouin light with high spectral extinction and low loss. We report background-free Brillouin spectra from Intralipid solutions and up to 100 μm deep within chicken muscle tissue.

  19. High-extinction virtually imaged phased array-based Brillouin spectroscopy of turbid biological media

    NASA Astrophysics Data System (ADS)

    Fiore, Antonio; Zhang, Jitao; Shao, Peng; Yun, Seok Hyun; Scarcelli, Giuliano

    2016-05-01

    Brillouin microscopy has recently emerged as a powerful technique to characterize the mechanical properties of biological tissue, cell, and biomaterials. However, the potential of Brillouin microscopy is currently limited to transparent samples, because Brillouin spectrometers do not have sufficient spectral extinction to reject the predominant non-Brillouin scattered light of turbid media. To overcome this issue, we combined a multi-pass Fabry-Perot interferometer with a two-stage virtually imaged phased array spectrometer. The Fabry-Perot etalon acts as an ultra-narrow band-pass filter for Brillouin light with high spectral extinction and low loss. We report background-free Brillouin spectra from Intralipid solutions and up to 100 μm deep within chicken muscle tissue.

  20. Infrared Extinction Coefficients of Aerosolized Conductive Flake Powders and Flake Suspensions having a Zero-Truncated Poisson Size Distribution

    DTIC Science & Technology

    2012-11-01

    A twin-fluid atomizing nozzle was used to disseminate all materials into a stirred 190 m 3 cylindrical aerosol chamber. After dispersion by the... nozzle and thorough chamber mixing with a low speed fan, spectral aerosol transmittance and concentration were simultaneously measured to obtain spectral...varying concentrations were prepared by stirring and sonicating the powders in ethanol. A twin-fluid atomizing nozzle , consisting of a jet of the

  1. Evaluating the impact of assimilating CALIOP-derived aerosol extinction profiles on a global mass transport model

    NASA Astrophysics Data System (ADS)

    Zhang, Jianglong; Campbell, James R.; Reid, Jeffrey S.; Westphal, Douglas L.; Baker, Nancy L.; Campbell, William F.; Hyer, Edward J.

    2011-07-01

    Coupled two/three-dimensional variational (2D/3DVAR) assimilation of aerosol physical properties retrieved from the Moderate Resolution Imaging Spectroradiometer (MODIS), Multi-angle Imaging Spectroradiometer (MISR) and Cloud Aerosol Lidar with Orthogonal Polarization (CALIOP) satellite-borne instruments is described for the U. S. Navy Aerosol Analysis and Prediction System (NAAPS) global aerosol mass transport model. Coupled 2D/3DVAR assimilation for NAAPS is evaluated for 48-hr forecast cycles, computed four times daily in six-hour intervals, versus stand-alone 2DVAR assimilation of MODIS and MISR aerosol optical depths (AOD). Both systems are validated against AERONET ground-based sun photometer measurements of AOD. Despite a narrow nadir viewing swath and more than 2700 km of equatorial separation between orbits, satellite lidar data assimilation elicits a positive model response. Improvements in analysis and forecast AOD absolute errors are found over both land and maritime AERONET sites. The primary impact to the model from 3DVAR assimilation is the redistribution of aerosol mass into the boundary layer, though the process is sensitive to parameterization of vertical error correlation lengths.

  2. SERRS and visible extinction spectroscopy of copper chlorophyllin on silver colloids as a function of pH.

    PubMed

    House, Paul G; Schnitzer, Cheryl S

    2008-02-15

    A study of sodium copper chlorophyllin adsorbed on silver colloids (CuChl/Ag) is conducted using surface-enhanced resonance Raman scattering (SERRS) and visible extinction spectroscopy to examine how the system changes as a function of pH. Initially at basic pH, SERRS signal is not detected even though CuChl is adsorbed onto the silver surface and deprotonated. Upon decreasing the solution pH slightly, colloidal aggregation is induced, evidenced by the broadening of the visible extinction spectra. The larger aggregates possess a surface plasmon that is in resonance with the laser excitation frequency (633-nm) and SERRS signal is detected. As the acid protonates CuChl, the overall negatively-charged surface approaches neutrality which induces more aggregation. Complete protonation of CuChl by pH 4.6 results in colloidal precipitation. However, when aggregation is halted about pH 5, adding NaOH(aq) to the system maintains the extent of aggregation and an intense SERRS signal is detected at basic pH.

  3. Simultaneous measurement of atmospheric temperature, humidity, and aerosol extinction and backscatter coefficients by a combined vibrational pure-rotational Raman lidar

    NASA Astrophysics Data System (ADS)

    Balin, I.; Serikov, I.; Bobrovnikov, S.; Simeonov, V.; Calpini, B.; Arshinov, Y.; van den Bergh, H.

    2004-10-01

    Implementation of the pure-rotational Raman (PRR) lidar method for simultaneous measurement of atmospheric temperature, humidity, and aerosol extinction and backscatter coefficients is reported. The isolation of two wavelength domains of the PRR spectrum and the suppression of the elastically scattered light is carried out by a double-grating polychromator. Experiments involving elastic backscatter from dense clouds and a solid target confirm the high level of suppression of the elastic light in the corresponding acquisition channels of the two selected PRR domains. Calibration of the temperature channel was done both by comparison with an experimentally verified atmospheric temperature model profile and by inter-comparison with radiosondes. Night-time temperature profiles with high vertical resolution were obtained up to the lower stratosphere. The PRR temperature profile combined with the water vapor mixing ratio obtained from the ro-vibrational Raman channel is used to estimate the relative humidity.

  4. Condensation nuclei and aerosol-scattering extinction measurements at Mauna Loa Observatory: 1974-1985. Data report

    SciTech Connect

    Massey, D.M.; Quakenbush, T.K.; Bodhaine, B.A.

    1987-07-01

    The observatory at Mauna Loa, Hawaii measures the characteristics of surface aerosols under background conditions. The instruments provide data that are representative of the background-aerosol climatology at Mauna Loa. These data can also be used to identify potential local contamination periods. The nephelometer's light-scattering measurements show an annual cycle: a maximum in April and a minimum in November, with a variation of a factor of 5.5. The Condensation Nucleus (CN) counter shows a much smaller annual cycle: a maximum in September and a minimum in March, with a variation of a factor of 1.5. A local decrease in CN concentration occurs in August. The Angstrom exponent minimum occurs in May. This indicates larger aerosol particles within the month as compared with the remainder of the year.

  5. Lidar conversion parameters derived from SAGE II extinction measurements

    NASA Technical Reports Server (NTRS)

    Thomason, L. W.; Osborn, M. T.

    1992-01-01

    SAGE II multiwavelength aerosol extinction measurements are used to estimate mass- and extinction-to-backscatter conversion parameters. The basis of the analysis is the principal component analysis of the SAGE II extinction kernels to estimate both total aerosol mass and aerosol backscatter at a variety of wavelengths. Comparisons of coincident SAGE II extinction profiles with 0.694-micron aerosol backscatter profiles demonstrate the validity of the method.

  6. Aircraft Measurements of BrO, IO, Glyoxal, NO2, H2O, O2-O2 and Aerosol Extinction Profiles in the Tropics: Comparison with Aircraft-/Ship-Based in Situ and Lidar Measurements

    NASA Technical Reports Server (NTRS)

    Volkamer, R.; Baidar, S.; Campos, T. L.; Coburn, S.; DiGangi, J. P.; Dix, B.; Eloranta, E. W.; Koenig, T. K.; Morley, B.; Ortega, I.; Pierce, B. R.; Reeves, M.; Sinreich, R.; Wang, S.; Zondlo, M. A.; Romashkin, P. A.

    2015-01-01

    Tropospheric chemistry of halogens and organic carbon over tropical oceans modifies ozone and atmospheric aerosols, yet atmospheric models remain largely untested for lack of vertically resolved measurements of bromine monoxide (BrO), iodine monoxide (IO) and small oxygenated hydrocarbons like glyoxal (CHOCHO) in the tropical troposphere. BrO, IO, glyoxal, nitrogen dioxide (NO2), water vapor (H2O) and O2-O2 collision complexes (O4/ were measured by the University of Colorado Airborne Multi-AXis Differential Optical Absorption Spectroscopy (CU AMAXDOAS) instrument, aerosol extinction by high spectral resolution lidar (HSRL), in situ aerosol size distributions by an ultra high sensitivity aerosol spectrometer (UHSAS) and in situ H2O by vertical-cavity surface-emitting laser (VCSEL) hygrometer. Data are presented from two research flights (RF12, RF17) aboard the National Science Foundation/ National Center for Atmospheric Research Gulfstream V aircraft over the tropical Eastern Pacific Ocean (tEPO) as part of the "Tropical Ocean tRoposphere Exchange of Reactive halogens and Oxygenated hydrocarbons" (TORERO) project (January/February 2012). We assess the accuracy of O4 slant column density (SCD) measurements in the presence and absence of aerosols. Our O4-inferred aerosol extinction profiles at 477 nm agree within 6% with HSRL in the boundary layer and closely resemble the renormalized profile shape of Mie calculations constrained by UHSAS at low (sub-Rayleigh) aerosol extinction in the free troposphere. CU AMAX-DOAS provides a flexible choice of geometry, which we exploit to minimize the SCD in the reference spectrum (SCDREF, maximize signal-to-noise ratio) and to test the robustness of BrO, IO and glyoxal differential SCDs. The RF12 case study was conducted in pristine marine and free tropospheric air. The RF17 case study was conducted above the NOAA RV Ka'imimoana (TORERO cruise, KA-12-01) and provides independent validation data from ship-based in situ cavity

  7. Aircraft measurements of BrO, IO, glyoxal, NO2, H2O, O2-O2 and aerosol extinction profiles in the tropics: comparison with aircraft-/ship-based in situ and lidar measurements

    NASA Astrophysics Data System (ADS)

    Volkamer, R.; Baidar, S.; Campos, T. L.; Coburn, S.; DiGangi, J. P.; Dix, B.; Eloranta, E. W.; Koenig, T. K.; Morley, B.; Ortega, I.; Pierce, B. R.; Reeves, M.; Sinreich, R.; Wang, S.; Zondlo, M. A.; Romashkin, P. A.

    2015-05-01

    Tropospheric chemistry of halogens and organic carbon over tropical oceans modifies ozone and atmospheric aerosols, yet atmospheric models remain largely untested for lack of vertically resolved measurements of bromine monoxide (BrO), iodine monoxide (IO) and small oxygenated hydrocarbons like glyoxal (CHOCHO) in the tropical troposphere. BrO, IO, glyoxal, nitrogen dioxide (NO2), water vapor (H2O) and O2-O2 collision complexes (O4) were measured by the University of Colorado Airborne Multi-AXis Differential Optical Absorption Spectroscopy (CU AMAX-DOAS) instrument, aerosol extinction by high spectral resolution lidar (HSRL), in situ aerosol size distributions by an ultra high sensitivity aerosol spectrometer (UHSAS) and in situ H2O by vertical-cavity surface-emitting laser (VCSEL) hygrometer. Data are presented from two research flights (RF12, RF17) aboard the National Science Foundation/National Center for Atmospheric Research Gulfstream V aircraft over the tropical Eastern Pacific Ocean (tEPO) as part of the "Tropical Ocean tRoposphere Exchange of Reactive halogens and Oxygenated hydrocarbons" (TORERO) project (January/February 2012). We assess the accuracy of O4 slant column density (SCD) measurements in the presence and absence of aerosols. Our O4-inferred aerosol extinction profiles at 477 nm agree within 6% with HSRL in the boundary layer and closely resemble the renormalized profile shape of Mie calculations constrained by UHSAS at low (sub-Rayleigh) aerosol extinction in the free troposphere. CU AMAX-DOAS provides a flexible choice of geometry, which we exploit to minimize the SCD in the reference spectrum (SCDREF, maximize signal-to-noise ratio) and to test the robustness of BrO, IO and glyoxal differential SCDs. The RF12 case study was conducted in pristine marine and free tropospheric air. The RF17 case study was conducted above the NOAA RV Ka'imimoana (TORERO cruise, KA-12-01) and provides independent validation data from ship-based in situ cavity

  8. Measured Infrared Absorption and Extinction Cross Sections for a Variety of Chemically and Biologically Derived Aerosol Simulants

    DTIC Science & Technology

    2004-06-01

    Aerosols considered are categorized as biological, chemical, and inorganic in origin, i.e., bacillus subtilis endospores, dimethicone silicone oil...achieved. The materials considered for this study include dimethicone silicone oil (SF-96 grade 50), bacillus subtilis endospores (BG), and Kaolin

  9. GMASS ultradeep spectroscopy of galaxies at z ~ 2. VI. Star formation, extinction, and gas outflows from UV spectra

    NASA Astrophysics Data System (ADS)

    Talia, M.; Mignoli, M.; Cimatti, A.; Kurk, J.; Berta, S.; Bolzonella, M.; Cassata, P.; Daddi, E.; Dickinson, M.; Franceschini, A.; Halliday, C.; Pozzetti, L.; Renzini, A.; Rodighiero, G.; Rosati, P.; Zamorani, G.

    2012-03-01

    Aims: We use rest-frame UV spectroscopy to investigate the properties related to large-scale gas outflow, and both the dust extinction and star-formation rates (SFRs) of a sample of z ~ 2 star-forming galaxies from the Galaxy Mass Assembly ultradeep Spectroscopic Survey (GMASS). Methods: Dust extinction is estimated from the rest-frame UV continuum slope and used to obtain dust-corrected SFRs for the galaxies in the sample. A composite spectrum is created by averaging all the single spectra of our sample, and the equivalent widths and centroids of the absorption lines associated with the interstellar medium are measured. We then calculate the velocity offsets of these lines relative to the composite systemic velocity, which is obtained from photospheric stellar absorption lines and nebular emission lines. Finally, to investigate correlations between galaxy UV spectral characteristics and galaxy general properties, the sample is divided into two bins that are equally populated, according to the galaxy properties of stellar mass, color excess, and SFR. A composite spectrum for each group of galaxies is then created, and both the velocity offsets and the equivalent widths of the interstellar absorption lines are measured. Results: For the entire sample, we derive a mean value of the continuum slope ⟨β⟩ = -1.11 ± 0.44 (rms). For each galaxy, we calculate the dust extinction from the UV spectrum and then use this to correct the flux measured at 1500 Å (rest-frame), before converting the corrected UV flux into a SFR. We find that our galaxies have an average SFR of ⟨SFR⟩ = 52 ± 48 M⊙ yr-1 (rms) and that there is a positive correlation between SFR and stellar mass, in agreement with other works, the logarithmic slope of the relation being 1.10 ± 0.10. We discover that the low-ionization absorption lines associated with the interstellar medium measured in the composite spectrum, are blueshifted with respect to the rest frame of the system, which indicates

  10. Simulation model of scattering properties and extinction of laser light applied to urban aerosols over the city of Cali, Colombia

    NASA Astrophysics Data System (ADS)

    Rodríguez, Edith; Montilla, Elena; Jaramillo, Mauricio; Solarte, Efraín; Bastidas, Alvaro

    2005-10-01

    Aerosols are among the most spatially variable components of the atmosphere, and thus their study requires their monitoring over a broad geographic range. The backscattering of light from suspended solid and liquid particles in the atmosphere obeys Mie scattering theory. Light attenuation in the spectral region from 300 to 4000 nm due to Mie scattering exceeds that due to molecular (Rayleigh) scattering and ozone absorption combined. This occurs despite the fact that aerosol particle concentrations in the atmosphere are many orders of magnitude smaller than molecular concentrations. Starting from the characteristics of urban aerosols measured over the city of Cali (Colombia), 3° 30' N, 76° 30' W, with a PM10 particle selector, along with information on meteorological conditions typical of the region, we present the results of a study of light scattering properties generated using a model applied Mie scattering theory to size parameter between 0 and 50, with an increment of 0.01, and Matlab computer code, to simulate and predict measurements with a Lidar system operating at 532 nm.

  11. Chemical Analysis of Individual Aerosols Particles by Electron Energy-Loss Spectroscopy (EELS)

    NASA Astrophysics Data System (ADS)

    Buseck, P. R.; Buseck, P. R.; Garvie, L. A.; Li, J.; Posfai, M.

    2001-12-01

    We use electron energy-loss spectroscopy (EELS) with a transmission electron microscope (TEM) to obtain chemical and bonding information on individual aerosol particles. EELS is ideally suited to this task because of its high spatial resolution and sensitivity to light elements such as C, N, and O. In addition, the spectral shapes provide information regarding bonding, atomic coordination and, for polyvalent elements, oxidation states. Our current focus is on carbonaceous aerosols both in the ambient air and emissions from biomass burning, with emphasis on the heterogeneous chemistry, particle structure, and chemical composition of soot particles. From the EELS spectra we were able to record for the first time, differences in composition between individual spherules within the same soot aggregate. We also found evidence of chemical variations even within individual soot spheres as small as 50 nm across. In the case of biomass burning, the most striking chemical differences are in the quantity of K, minor O and, in places, N. The quantity of elements associated with C decreases with the degree of graphitization of the soot spheres, as shown by the shapes of the C spectra and was corroborated by high-resolution TEM images of the analyzed particles. Knowledge of the degree of graphitization and quantity of associated elements is important for understanding and modeling their optical properties and in some case in source attributions.

  12. Laser-Induced Breakdown Spectroscopy (LIBS) in a Novel Molten Salt Aerosol System.

    PubMed

    Williams, Ammon N; Phongikaroon, Supathorn

    2017-04-01

    In the pyrochemical separation of used nuclear fuel (UNF), fission product, rare earth, and actinide chlorides accumulate in the molten salt electrolyte over time. Measuring this salt composition in near real-time is advantageous for operational efficiency, material accountability, and nuclear safeguards. Laser-induced breakdown spectroscopy (LIBS) has been proposed and demonstrated as a potential analytical approach for molten LiCl-KCl salts. However, all the studies conducted to date have used a static surface approach which can lead to issues with splashing, low repeatability, and poor sample homogeneity. In this initial study, a novel molten salt aerosol approach has been developed and explored to measure the composition of the salt via LIBS. The functionality of the system has been demonstrated as well as a basic optimization of the laser energy and nebulizer gas pressure used. Initial results have shown that this molten salt aerosol-LIBS system has a great potential as an analytical technique for measuring the molten salt electrolyte used in this UNF reprocessing technology.

  13. Understanding hygroscopic growth and phase transformation of aerosols using single particle Raman spectroscopy in an electrodynamic balance.

    PubMed

    Lee, Alex K Y; Ling, T Y; Chan, Chak K

    2008-01-01

    Hygroscopic growth is one of the most fundamental properties of atmospheric aerosols. By absorbing or evaporating water, an aerosol particle changes its size, morphology, phase, chemical composition and reactivity and other parameters such as its refractive index. These changes affect the fate and the environmental impacts of atmospheric aerosols, including global climate change. The ElectroDynamic Balance (EDB) has been widely accepted as a unique tool for measuring hygroscopic properties and for investigating phase transformation of aerosols via single particle levitation. Coupled with Raman spectroscopy, an EDB/Raman system is a powerful tool that can be used to investigate both physical and chemical changes associated with the hygroscopic properties of individually levitated particles under controlled environments. In this paper, we report the use of an EDB/Raman system to investigate (1) contact ion pairs formation in supersaturated magnesium sulfate solutions; (2) phase transformation in ammonium nitrate/ammonium sulfate mixed particles; (3) hygroscopicity of organically coated inorganic aerosols; and (4) heterogeneous reactions altering the hygroscopicity of organic aerosols.

  14. Data Fusion of Imaging Spectroscopy, Lidar, and In-Situ Laboratory Data for Detecting Aerosols from Biomass Burning Events

    NASA Astrophysics Data System (ADS)

    McCubbin, I. B.; Arnott, W. P.; Schläpfer, D.; McGill, M.

    2007-12-01

    Aerosols absorb and scatter solar and thermal infrared radiation, thereby altering the radiative balance of the Earth-atmosphere system. This is called the aerosol direct effect. Remote sensing of aerosols from satellites is essential to obtain the contribution of anthropogenic emission to the radiative balance. It is necessary to be able to map their presence and abundance using remote measurements. If we can quantify the occurrence of aerosols from biomass burning using remote sensing, we can improve our understanding of the direct radiative effect. This study uses airborne remote sensing data to understand, identify, and quantify smoke aerosols in the atmosphere. In particular, using Imaging Spectroscopy and lidar data to detect the presence and abundance of aerosols. Airborne remote sensing data was collected over the active Simi Valley wildfire on October 27, 2003 in Southern California. The Airborne Visible and Infrared Imaging Spectrometer (AVIRIS) was flown on a commercially operated Twin Otter aircraft at an altitude of 6 km, and collected 224 channels of radiance data from 380 - 2400 nm with 10 nm spectral resolution. Shortly after the AVIRIS data collection, the Cloud Physics Lidar (CPL) was flown on the NASA ER-2 at an altitude of 20 km. CPL is a three wavelength instrument that operates at 1064, 532, and 355 nm, with a 30 m vertical and 200 m horizontal resolution. Controlled laboratory measurements of aerosol optics from burning various woods and grasses provide insight and refinement of our understanding of remote sensing data for biomass burning aerosol. In 2006 and 2007 a two-phase project was conducted at the US Forest Service's Fire Science Laboratory to characterize particulate matter generated by biomass burning. The Fire Lab at Missoula Experiment (FLAME) is supported by the Joint Fire Science Program and is a cooperative effort between the National Park Service, the Desert Research Institute, and Colorado State University. FLAME was a series

  15. Vertical profiles of aerosol volume from high-spectral-resolution infrared transmission measurements. I. Methodology.

    PubMed

    Eldering, A; Irion, F W; Chang, A Y; Gunson, M R; Mills, F P; Steele, H M

    2001-06-20

    The wavelength-dependent aerosol extinction in the 800-1250-cm(-1) region has been derived from ATMOS (atmospheric trace molecule spectroscopy) high-spectral-resolution IR transmission measurements. Using models of aerosol and cloud extinction, we have performed weighted nonlinear least-squares fitting to determine the aerosol-volume columns and vertical profiles of stratospheric sulfate aerosol and cirrus cloud volume. Modeled extinction by use of cold-temperature aerosol optical constants for a 70-80% sulfuric-acid-water solution shows good agreement with the measurements, and the derived aerosol volumes for a 1992 occultation are consistent with data from other experiments after the eruption of Mt. Pinatubo. The retrieved sulfuric acid aerosol-volume profiles are insensitive to the aerosol-size distribution and somewhat sensitive to the set of optical constants used. Data from the nonspherical cirrus extinction model agree well with a 1994 mid-latitude measurement indicating the presence of cirrus clouds at the tropopause.

  16. Phase transition behaviour of sodium oleate aerosol particles

    NASA Astrophysics Data System (ADS)

    Nájera, Juan J.

    Field measurements have shown that organic surfactants are significant components of atmospheric aerosols. While fatty acids, among other surfactants, are prevalent in the atmosphere, the influence of these species on the chemical and physical properties of atmospheric aerosols remains not fully characterized. In order to assess the phase in which particles may exist, a detailed study of the deliquescence of a model surfactant aerosol has been carried out. Sodium oleate was chosen as a surfactant proxy relevant in atmospheric aerosol. Sodium oleate micelle aerosol particles were generated nebulizing a sodium oleate aqueous solution. In this study, the water uptake and phase transition of sodium oleate aerosol particles have been studied in a room temperature aerosol flow tube system (AFT) using Fourier transform infrared (FTIR) spectroscopy. Aerosol morphology and elemental composition were also analysed using scanning electron microscopy/energy dispersive X-ray analysis (SEM/EDX) techniques. The particles are homogeneously distributed as ellipsoidal-shape aggregates of micelles particles with an average size of ˜1.1 μm. The deliquescence by the sodium oleate aerosol particles was monitored by infrared extinction spectroscopy, where the dried aerosol particles were exposed to increasing relative humidity as they passed through the AFT. Observations of the infrared absorption features of condensed phase liquid water enable to determine the sodium oleate deliquescence phase transition at 88±2%.

  17. Characterization of atmospheric aerosols in the Adirondack Mountains using PIXE, SEM/EDX, and Micro-Raman spectroscopies

    NASA Astrophysics Data System (ADS)

    Vineyard, M. F.; LaBrake, S. M.; Ali, S. F.; Nadareski, B. J.; Safiq, A. D.; Smith, J. W.; Yoskowitz, J. T.

    2015-05-01

    We are making detailed measurements of the composition of atmospheric aerosols collected in the Adirondack Mountains as a function of particle size using proton-induced X-ray emission, scanning electron microscopy with energy-dispersive X-ray spectroscopy, and Micro-Raman spectroscopy. These measurements provide valuable data to help identify the sources and understand the transport, transformation, and effects of airborne pollutants in upstate New York. Preliminary results indicate significant concentrations of sulfur in small particles that can travel great distances, and that this sulfur may be in the form of oxides that can contribute to acid rain.

  18. Micro-Raman Spectroscopy to Complement Proton-Induced X-Ray Emission in the Analysis of Atmospheric Aerosols

    NASA Astrophysics Data System (ADS)

    Safiq, Alexandrea; Ali, Salina; Nadarski, Benjamin; Smith, Jeremy; Yoskowitz, Josh; Labrake, Scott; Vineyard, Michael; Union College Team

    2013-10-01

    There is an active research program in the Union College Ion-Beam Analysis Laboratory on proton-induced X-ray emission (PIXE) analysis of atmospheric aerosols. PIXE is a powerful tool for the study of airborne pollution because it provides information on a broad range of elements simultaneously, has low detection limits, is nondestructive, does not require large samples, and the analysis can be performed in a short amount of time. However, PIXE provides only elemental information. We are investigating the use of Micro-Raman spectroscopy (MRS) to complement PIXE analysis of aerosol samples by providing chemical information. In MRS, laser light is inelastically scattered from a sample and the vibrational spectrum of the scattered light is used to identify molecules and their functional groups. We are focusing on aerosol samples collected in the Adirondack Mountains that have considerable concentrations of sulfur that may contribute to acid rain. The MRS spectra collected on aerosol samples are being compared with a library of standards to try to determine the molecular structures in which the sulfur is bound. We will describe the analysis and present preliminary results. Union College Undergraduate Research Program.

  19. New Approach for Near-Real-Time Measurement of Elemental Composition of Aerosol Using Laser-Induced Breakdown Spectroscopy

    PubMed Central

    Diwakar, Prasoon; Kulkarni, Pramod; Birch, M. Eileen

    2015-01-01

    A new approach has been developed for making near-real-time measurement of elemental composition of aerosols using plasma spectroscopy. The method allows preconcentration of miniscule particle mass (pg to ng) directly from the sampled aerosol stream through electrostatic deposition of charged particles (30–900 nm) onto a flat-tip microneedle electrode. The collected material is subsequently ablated from the electrode and monitored by laser-induced breakdown spectroscopy. Atomic emission spectra were collected using a broadband spectrometer with a wavelength range of 200–980 nm. A single-sensor delay time of 1.3 μs was used in the spectrometer for all elements to allow simultaneous measurement of multiple elements. The system was calibrated for various elements including Cd, Cr, Cu, Mn, Na, and Ti. The absolute mass detection limits for these elements were experimentally determined and found to be in the range of 0.018–5 ng. The electrostatic collection technique has many advantages over other substrate-based methods involving aerosol collection on a filter or its focused deposition using an aerodynamic lens. Because the particle mass is collected over a very small area that is smaller than the spatial extent of the laser-induced plasma, the entire mass is available for analysis. This considerably improves reliability of the calibration and enhances measurement accuracy and precision. Further, the aerosol collection technique involves very low pressure drop, thereby allowing higher sample flow rates with much smaller pumps—a desirable feature for portable instrumentation. Higher flow rates also make it feasible to measure trace element concentrations at part per trillion levels. Detection limits in the range of 18–670 ng m−3 can be achieved for most of the elements studied at a flow rate of 1.5 L min−1 with sampling times of 5 min. PMID:26692632

  20. New Approach for Near-Real-Time Measurement of Elemental Composition of Aerosol Using Laser-Induced Breakdown Spectroscopy.

    PubMed

    Diwakar, Prasoon; Kulkarni, Pramod; Birch, M Eileen

    A new approach has been developed for making near-real-time measurement of elemental composition of aerosols using plasma spectroscopy. The method allows preconcentration of miniscule particle mass (pg to ng) directly from the sampled aerosol stream through electrostatic deposition of charged particles (30-900 nm) onto a flat-tip microneedle electrode. The collected material is subsequently ablated from the electrode and monitored by laser-induced breakdown spectroscopy. Atomic emission spectra were collected using a broadband spectrometer with a wavelength range of 200-980 nm. A single-sensor delay time of 1.3 μs was used in the spectrometer for all elements to allow simultaneous measurement of multiple elements. The system was calibrated for various elements including Cd, Cr, Cu, Mn, Na, and Ti. The absolute mass detection limits for these elements were experimentally determined and found to be in the range of 0.018-5 ng. The electrostatic collection technique has many advantages over other substrate-based methods involving aerosol collection on a filter or its focused deposition using an aerodynamic lens. Because the particle mass is collected over a very small area that is smaller than the spatial extent of the laser-induced plasma, the entire mass is available for analysis. This considerably improves reliability of the calibration and enhances measurement accuracy and precision. Further, the aerosol collection technique involves very low pressure drop, thereby allowing higher sample flow rates with much smaller pumps-a desirable feature for portable instrumentation. Higher flow rates also make it feasible to measure trace element concentrations at part per trillion levels. Detection limits in the range of 18-670 ng m(-3) can be achieved for most of the elements studied at a flow rate of 1.5 L min(-1) with sampling times of 5 min.

  1. Analysis of functional groups in atmospheric aerosols by infrared spectroscopy: sparse methods for statistical selection of relevant absorption bands

    NASA Astrophysics Data System (ADS)

    Takahama, Satoshi; Ruggeri, Giulia; Dillner, Ann M.

    2016-07-01

    Various vibrational modes present in molecular mixtures of laboratory and atmospheric aerosols give rise to complex Fourier transform infrared (FT-IR) absorption spectra. Such spectra can be chemically informative, but they often require sophisticated algorithms for quantitative characterization of aerosol composition. Naïve statistical calibration models developed for quantification employ the full suite of wavenumbers available from a set of spectra, leading to loss of mechanistic interpretation between chemical composition and the resulting changes in absorption patterns that underpin their predictive capability. Using sparse representations of the same set of spectra, alternative calibration models can be built in which only a select group of absorption bands are used to make quantitative prediction of various aerosol properties. Such models are desirable as they allow us to relate predicted properties to their underlying molecular structure. In this work, we present an evaluation of four algorithms for achieving sparsity in FT-IR spectroscopy calibration models. Sparse calibration models exclude unnecessary wavenumbers from infrared spectra during the model building process, permitting identification and evaluation of the most relevant vibrational modes of molecules in complex aerosol mixtures required to make quantitative predictions of various measures of aerosol composition. We study two types of models: one which predicts alcohol COH, carboxylic COH, alkane CH, and carbonyl CO functional group (FG) abundances in ambient samples based on laboratory calibration standards and another which predicts thermal optical reflectance (TOR) organic carbon (OC) and elemental carbon (EC) mass in new ambient samples by direct calibration of infrared spectra to a set of ambient samples reserved for calibration. We describe the development and selection of each calibration model and evaluate the effect of sparsity on prediction performance. Finally, we ascribe

  2. [Characteristics and Parameterization for Atmospheric Extinction Coefficient in Beijing].

    PubMed

    Chen, Yi-na; Zhao, Pu-sheng; He, Di; Dong, Fan; Zhao, Xiu-juan; Zhang, Xiao-ling

    2015-10-01

    In order to study the characteristics of atmospheric extinction coefficient in Beijing, systematic measurements had been carried out for atmospheric visibility, PM2.5 concentration, scattering coefficient, black carbon, reactive gases, and meteorological parameters from 2013 to 2014. Based on these data, we compared some published fitting schemes of aerosol light scattering enhancement factor [ f(RH)], and discussed the characteristics and the key influence factors for atmospheric extinction coefficient. Then a set of parameterization models of atmospheric extinction coefficient for different seasons and different polluted levels had been established. The results showed that aerosol scattering accounted for more than 94% of total light extinction. In the summer and autumn, the aerosol hygroscopic growth caused by high relative humidity had increased the aerosol scattering coefficient by 70 to 80 percent. The parameterization models could reflect the influencing mechanism of aerosol and relative humidity upon ambient light extinction, and describe the seasonal variations of aerosol light extinction ability.

  3. Infrared spectroscopy of homogeneously nucleated hydrazine aerosols - Disordered and crystalline phases. [in planetary atmospheres

    NASA Technical Reports Server (NTRS)

    Dunder, T.; Clapp, M. L.; Miller, R. E.

    1993-01-01

    It is shown that aerosols generated at low temperatures and high condensation rate spontaneously form in a highly crystalline state. The resonant absorption bands in the IR spectra of these highly crystalline particles are much sharper than any reported previously in the bulk, and reveal details in the N-H vibrational bands that have not been previously observed. A disordered phase is also observed at somewhat higher temperatures. These results are consistent with this being a supercooled liquid. The fact that the spectra associated with these two aerosol phases are quite different is important to any future attempts at detecting hydrazine aerosols in planetary atmospheres by remote sensing techniques.

  4. A study of phase transformations in hygroscopic aerosols by Raman spectroscopy

    SciTech Connect

    Tang, I.N.; Fung, K.H.

    1995-12-31

    Atmospheric aerosol particles are composed mostly of hygroscopic inorganic salts. These aerosols play an important role in many atmospheric processes which affect local air quality, visibility degradation, and the global climate as well. Indeed, hygroscopic aerosols as metastable supersaturated solution droplets are routinely observed in laboratories. Here, we report first spectroscopic evidence that new metastable solid states form from hygroscopic aerosol particles. Levitated single particles undergo hydration and crystallization in calibrated humidity environment. Laser Raman and Mie scattering techniques are used to probe the chemical and physical state of the microparticle before and after phase transformation. The formation of these states is not predicted from bulk-phase thermodynamics. In some cases, the resulting metastable state is entirely unknown heretofore. We also present new solid/solution and solid/solid phase transitions which occur exclusively in microparticles.

  5. Stand-off detection of aerosols using mid-infrared backscattering Fourier transform spectroscopy

    NASA Astrophysics Data System (ADS)

    Maidment, L.; Zhang, Z.; Bowditch, M. D.; Howle, C. R.; Reid, D. T.

    2016-10-01

    The spectrum of mid-infrared light scattered from an actively illuminated aerosol was used to distinguish between different chemicals. Using spectrally broad illumination from an optical parametric oscillator covering 3.2 - 3.55 μm, characteristic absorption features of two different chemicals were detected, and two similar molecules were clearly distinguished using the spectra of backscattered light from each chemical aerosol.

  6. 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.

  7. 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

  8. 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.

  9. Discriminating Bio-aerosols from Non-Bio-aerosols in Real-Time by Pump-Probe Spectroscopy.

    PubMed

    Sousa, Gustavo; Gaulier, Geoffrey; Bonacina, Luigi; Wolf, Jean-Pierre

    2016-09-13

    The optical identification of bioaerosols in the atmosphere and its discrimination against combustion related particles is a major issue for real-time, field compatible instruments. In the present paper, we show that by embedding advanced pump-probe depletion spectroscopy schemes in a portable instrument, it is possible to discriminate amino acid containing airborne particles (bacteria, humic particles, etc.) from poly-cyclic aromatic hydrocarbon containing combustion particles (Diesel droplets, soot, vehicle exhausts) with high selectivity. Our real-time, multi-modal device provides, in addition to the pump-probe depletion information, fluorescence spectra (over 32 channels), fluorescence lifetime and Mie scattering patterns of each individually flowing particle in the probed air.

  10. Discriminating Bio-aerosols from Non-Bio-aerosols in Real-Time by Pump-Probe Spectroscopy

    NASA Astrophysics Data System (ADS)

    Sousa, Gustavo; Gaulier, Geoffrey; Bonacina, Luigi; Wolf, Jean-Pierre

    2016-09-01

    The optical identification of bioaerosols in the atmosphere and its discrimination against combustion related particles is a major issue for real-time, field compatible instruments. In the present paper, we show that by embedding advanced pump-probe depletion spectroscopy schemes in a portable instrument, it is possible to discriminate amino acid containing airborne particles (bacteria, humic particles, etc.) from poly-cyclic aromatic hydrocarbon containing combustion particles (Diesel droplets, soot, vehicle exhausts) with high selectivity. Our real-time, multi-modal device provides, in addition to the pump-probe depletion information, fluorescence spectra (over 32 channels), fluorescence lifetime and Mie scattering patterns of each individually flowing particle in the probed air.

  11. Discriminating Bio-aerosols from Non-Bio-aerosols in Real-Time by Pump-Probe Spectroscopy

    PubMed Central

    Sousa, Gustavo; Gaulier, Geoffrey; Bonacina, Luigi; Wolf, Jean-Pierre

    2016-01-01

    The optical identification of bioaerosols in the atmosphere and its discrimination against combustion related particles is a major issue for real-time, field compatible instruments. In the present paper, we show that by embedding advanced pump-probe depletion spectroscopy schemes in a portable instrument, it is possible to discriminate amino acid containing airborne particles (bacteria, humic particles, etc.) from poly-cyclic aromatic hydrocarbon containing combustion particles (Diesel droplets, soot, vehicle exhausts) with high selectivity. Our real-time, multi-modal device provides, in addition to the pump-probe depletion information, fluorescence spectra (over 32 channels), fluorescence lifetime and Mie scattering patterns of each individually flowing particle in the probed air. PMID:27619546

  12. [Development of a photoacoustic spectroscopy system for the measurement of absorption coefficient of atmospheric aerosols].

    PubMed

    Liu, Qiang; Niu, Ming-Sheng; Wang, Gui-Shi; Cao, Zhen-Song; Liu, Kun; Chen, Wei-Dong; Gao, Xiao-Ming

    2013-07-01

    In the present paper, the authors focus on the effect of the resonance frequency shift due to the changes in temperature and humidity on the PA signal, present several methods to control the noise derived form gas flow and vibration from the sampling pump. Based on the efforts mentioned above, a detection limit of 1.4 x 10(-8) W x cm(-1) x Hz(-1/2) was achieved for the measurement of atmospheric aerosols absorption coefficient. During the experiments, the PA cell was calibrated with the absorption of standard NO2 gas at 532 nm and the atmospheric aerosols were measured continuously. The measurement results show that the PAS is suitable for the real-time measurement of the absorption coefficient of atmospheric aerosols in their natural suspended state.

  13. Measurement of Aerosol Optical Properties by Integrating Cavity Ring-Down Spectroscopy and Nephelometry

    DTIC Science & Technology

    2013-01-01

    and agricultural burning. Mineral dust is formed from storms over arid areas such as the Sahara desert. Dust particles can be transported several...CLASSIFICATION OF: We measure scattering coefficient , extinction coefficient , scattering cross-section and single scattering albedo of 102, 203 and 296...We compared experimental optical property measurements with Mie theory predicted values. The scattering coefficient and scattering cross-section

  14. Series cell light extinction monitor

    DOEpatents

    Novick, Vincent J.

    1990-01-01

    A method and apparatus for using the light extinction measurements from two or more light cells positioned along a gasflow chamber in which the gas volumetric rate is known to determine particle number concentration and mass concentration of an aerosol independent of extinction coefficient and to determine estimates for particle size and mass concentrations. The invention is independent of particle size. This invention has application to measurements made during a severe nuclear reactor fuel damage test.

  15. Discrimination and classification of bio-aerosol particles using optical spectroscopy and scattering

    NASA Astrophysics Data System (ADS)

    Eversole, Jay D.

    2011-03-01

    For more than a decade now, there has been significant emphasis for development of sensors of agent aerosols, especially for biological warfare (BW) agents. During this period, the Naval Research Laboratory (NRL) and other labs have explored the application of optical and spectroscopic methods relevant to biological composition discrimination to aerosol particle characterization. I will first briefly attempt to establish the connection between sensor performance metrics which are statistically determined, and aerosol particle measurements through the use of computational models, and also describe the challenge of ambient background characterization that would be needed to establish more reliable and deterministic sensor performance predictions. Greater attention will then be devoted to a discussion of basic particle properties and their measurement. The NRL effort has adopted an approach based on direct measurements on individual particles, principally of elastic scatter and laser-induced fluorescence (LIF), rather than populations of particles. The development of a LIF instrument using two sequential excitation wavelengths to detect fluorescence in discrete spectral bands will be described. Using this instrument, spectral characteristics of particles from a variety of biological materials including BW agent surrogates, as well as other ``calibration'' particles and some known ambient air constituents will be discussed in terms of the dependence of optical signatures on aerosol particle composition, size and incident laser fluence. Comparison of scattering and emission measurements from particles composed of widely different taxa, as well as from similar species under different growth conditions highlight the difficulties of establishing ground truth for complex biological material compositions. One aspect that is anticipated to provide greater insight to this type of particle classification capability is the development of a fundamental computational model of

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

    NASA Technical Reports Server (NTRS)

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

    2012-01-01

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

  17. Optical and physical properties of stratospheric aerosols from balloon measurements in the visible and near-infrared domains. III. Presence of aerosols in the middle stratosphere.

    PubMed

    Renard, Jean-Baptiste; Ovarlez, Joëlle; Berthet, Gwenaël; Fussen, Didier; Vanhellemont, Filip; Brogniez, Colette; Hadamcik, Edith; Chartier, Michel; Ovarlez, Henri

    2005-07-01

    The aerosol extinction measurements in the ultraviolet and visible wavelengths by the balloonborne spectrometer Spectroscopie d'Absorption Lunaire pour l'Observation des Minoritaires Ozone et NOx (SALOMON) show that aerosols are present in the middle stratosphere, above 25-km altitude. These observations are confirmed by the extinction measurements performed by a solar occultation radiometer. The balloonborne Laboratoire de Météorologie Dynamique (LMD) counter instrument also confirms the presence of aerosol around 30-km altitude, with an unrealistic excess of micronic particles assuming that only liquid sulfate aerosols are present. An unexpected spectral structure around 640-nm observed by SALOMON is also detectable in extinction measurements by the satellite instrument Stratospheric Aerosols and Gas Experiment III. This set of measurements could indicate that solid aerosols were detected at these altitude ranges. The amount of soot detected up to now in the lower stratosphere is too low to explain these measurements. Thus, the presence of interplanetary dust grains and micrometeorites may need to be invoked. Moreover, it seems that these grains fill the stratosphere in stratified layers.

  18. Optical and physical properties of stratospheric aerosols from balloon measurements in the visible and near-infrared domains. III. Presence of aerosols in the middle stratosphere

    NASA Astrophysics Data System (ADS)

    Renard, Jean-Baptiste; Ovarlez, Joëlle; Berthet, Gwenaël; Fussen, Didier; Vanhellemont, Filip; Brogniez, Colette; Hadamcik, Edith; Chartier, Michel; Ovarlez, Henri

    2005-07-01

    The aerosol extinction measurements in the ultraviolet and visible wavelengths by the balloonborne spectrometer Spectroscopie d'Absorption Lunaire pour l'Observation des Minoritaires Ozone et NO_x (SALOMON) show that aerosols are present in the middle stratosphere, above 25-km altitude. These observations are confirmed by the extinction measurements performed by a solar occultation radiometer. The balloonborne Laboratoire de Météorologie Dynamique (LMD) counter instrument also confirms the presence of aerosol around 30-km altitude, with an unrealistic excess of micronic particles assuming that only liquid sulfate aerosols are present. An unexpected spectral structure around 640-nm observed by SALOMON is also detectable in extinction measurements by the satellite instrument Stratospheric Aerosols and Gas Experiment III. This set of measurements could indicate that solid aerosols were detected at these altitude ranges. The amount of soot detected up to now in the lower stratosphere is too low to explain these measurements. Thus, the presence of interplanetary dust grains and micrometeorites may need to be invoked. Moreover, it seems that these grains fill the stratosphere in stratified layers.

  19. Rethinking Extinction

    PubMed Central

    Dunsmoor, Joseph E.; Niv, Yael; Daw, Nathaniel; Phelps, Elizabeth A.

    2015-01-01

    Extinction serves as the leading theoretical framework and experimental model to describe how learned behaviors diminish through absence of anticipated reinforcement. In the past decade, extinction has moved beyond the realm of associative learning theory and behavioral experimentation in animals and has become a topic of considerable interest in the neuroscience of learning, memory, and emotion. Here, we review research and theories of extinction, both as a learning process and as a behavioral technique, and consider whether traditional understandings warrant a re-examination. We discuss the neurobiology, cognitive factors, and major computational theories, and revisit the predominant view that extinction results in new learning that interferes with expression of the original memory. Additionally, we reconsider the limitations of extinction as a technique to prevent the relapse of maladaptive behavior, and discuss novel approaches, informed by contemporary theoretical advances, that augment traditional extinction methods to target and potentially alter maladaptive memories. PMID:26447572

  20. Rethinking Extinction.

    PubMed

    Dunsmoor, Joseph E; Niv, Yael; Daw, Nathaniel; Phelps, Elizabeth A

    2015-10-07

    Extinction serves as the leading theoretical framework and experimental model to describe how learned behaviors diminish through absence of anticipated reinforcement. In the past decade, extinction has moved beyond the realm of associative learning theory and behavioral experimentation in animals and has become a topic of considerable interest in the neuroscience of learning, memory, and emotion. Here, we review research and theories of extinction, both as a learning process and as a behavioral technique, and consider whether traditional understandings warrant a re-examination. We discuss the neurobiology, cognitive factors, and major computational theories, and revisit the predominant view that extinction results in new learning that interferes with expression of the original memory. Additionally, we reconsider the limitations of extinction as a technique to prevent the relapse of maladaptive behavior and discuss novel approaches, informed by contemporary theoretical advances, that augment traditional extinction methods to target and potentially alter maladaptive memories.

  1. Development of infrared photothermal deflection spectroscopy (mirage effect) for analysis of condensed-phase aerosols collected in a micro-orifice uniform deposit impactor.

    PubMed

    Dada, Oluwatosin O; Bialkowski, Stephen E

    2008-12-01

    The potential of mid-infrared photothermal deflection spectrometry for aerosol analysis is demonstrated. Ammonium nitrate aerosols are deposited on a flat substrate using a micro-orifice uniform deposit impactor (MOUDI). Photothermal spectroscopy with optical beam deflection (mirage effect) is used to detect deposited aerosols. Photothermal deflection from aerosols is measured by using pulsed infrared laser light to heat up aerosols collected on the substrate. The deflection signal is obtained by measuring the position of a spot from a beam of light as it passes near the heated surface. The results indicate non-rotating impaction as the preferred MOUDI impaction method. Energy-dependent photothermal measurement shows a linear relationship between signal and laser intensity, and no loss of signal with time is observed. The detection limit from the signal-mass curve is 7.31 ng. For 30 minutes collection time and 30 L/min flow rate of the impactor, the limit of detection in terms of aerosol mass concentration is 0.65 microg m(-3).

  2. Gas Phase Spectroscopy of Cold PAH Ions: Contribution to the Interstellar Extinction and the Diffuse Interstellar Bands

    NASA Technical Reports Server (NTRS)

    Biennier, L.; Salama, F.; Allamandola, L. J.; Scherer, J. J.; OKeefe, A.

    2002-01-01

    Polycyclic Aromatic Hydrocarbon molecules (PAHs) are ubiquitous in the interstellar medium (ISM) and constitute the building blocks of interstellar dust grains. Despite their inferred important role in mediating the energetic and chemical processes in thc ISM, their exact contribution to the interstellar extinction, and in particular to the diffuse interstellar bands (DIBs) remains unclear. The DIBs are spectral absorption features observed in the line of sight of stars that are obscured by diffuse interstellar clouds. More than 200 bands have been reported to date spanning from the near UV to the near IR with bandwidths ranging from 0.4 to 40 Angstroms (Tielens & Snow 1995). The present consensus is that the DIBs arise from free flying, gas-phase, organic molecules and/or ions that are abundant under the typical conditions reigning in the diffuse ISM. PAHs have been proposed as possible carriers (Allamandola et al. 1985; Leger & DHendecourt 1985). The PAH hypothesis is consistent with the cosmic abundance of Carbon and Hydrogen and with the required photostability of the DIB carriers against the strong VUV radiation field in the diffuse interstellar clouds. A significant fraction of PAHs is expected to be ionized in the diffuse ISM.

  3. The complex, dusty narrow-line region of NGC 4388: gas-jet interactions, outflows and extinction revealed by near-IR spectroscopy

    NASA Astrophysics Data System (ADS)

    Rodríguez-Ardila, A.; Mason, R. E.; Martins, L.; Ramos Almeida, C.; Riffel, R. A.; Riffel, R.; Lira, P.; González Martín, O.; Dametto, N. Z.; Flohic, H.; Ho, L. C.; Ruschel-Dutra, D.; Thanjavur, K.; Colina, L.; McDermid, R. M.; Perlman, E.; Winge, C.

    2017-02-01

    We present Gemini/GNIRS (Gemini Near-Infrared Spectrograph) spectroscopy of the Seyfert 2 galaxy NGC 4388, with simultaneous coverage from 0.85 to 2.5 μm. Several spatially extended emission lines are detected for the first time, both in the obscured and unobscured portion of the optical narrow-line region (NLR), allowing us to assess the combined effects of the central continuum source, outflowing gas and shocks generated by the radio jet on the central 280 pc gas. The H I and [Fe II] lines allow us to map the extinction affecting the NLR. We found that the nuclear region is heavily obscured, with E(B - V) ˜ 1.9 mag. To the NE of the nucleus and up to ˜150 pc, the extinction remains large, ˜1 mag or larger, consistent with the system of dust lanes seen in optical imaging. We derived position-velocity diagrams for the most prominent lines as well as for the stellar component. Only the molecular gas and the stellar component display a well-organized pattern consistent with disc rotation. Other emission lines are kinematically perturbed or show little evidence of rotation. Extended high-ionization emission of sulphur, silicon and calcium is observed to distances of at least 200 pc both NE and SW of the nucleus. We compared flux ratios between these lines with photoionization models and conclude that radiation from the central source alone cannot explain the observed high-ionization spectrum. Shocks between the radio jet and the ambient gas are very likely an additional source of excitation. We conclude that NGC 4388 is a prime laboratory to study the interplay between all these mechanisms.

  4. Extinction, emission, and scattering spectroscopy of 5-50 nm citrate-coated gold nanoparticles: An argument for curvature effects on aggregation.

    PubMed

    Esfahani, Milad Rabbani; Pallem, Vasanta L; Stretz, Holly A; Wells, Martha J M

    2017-03-15

    The interaction of macromolecules with gold nanoparticles (GNPs) is of interest in the emerging field of biomedical and environmental detection devices. However, the physicochemical properties, including spectra, of GNPs in aqueous solution in the absence of metal-macromolecular interactions must first be considered before their activity in biological and environmental systems can be understood. The specific objective of this research was to experimentally illuminate the role of nanoparticle core size on the spectral (simultaneous consideration of extinction, emission, and scattering) versus aggregation behaviors of citrate-coated GNPs (CT-GNPs). It is difficult to find in the literature systematic simultaneous presentation of scattering, emission, and extinction spectra, including the UV range, and thus the present work will aid those who would use such particles for spectroscopic related separations or sensors. The spectroscopic behavior of CT-GNPs with different core sizes (5, 10, 30, and 50nm) was studied in ultra-pure water at pH6.0-6.5 employing UV-visible extinction, excitation-emission matrix (EEM), resonance Rayleigh scattering, and dynamic light scattering (DLS) spectroscopies. The CT-GNP-5 and CT-GNP-10 samples aggregated, absorbed light, and emitted light. In contrast, the CT-GNP-30 and CT-GNP-50 samples did not aggregate and did not emit light, but scattered light intensely. Multimodal peaks were observed in the intensity-based DLS spectra of CT-GNP-5 and CT-GNP-10 samples. Monomodal peaks in the volume-based DLS spectra overestimated particle diameters by 60% and 30% for the CT-GNP-5 and CT-GNP-10 samples, respectively, but underestimated diameters by 10% and 4% for the CT-GNP-30 and CT-GNP-50 samples. The volume-based DLS spectra indicated that dimer and trimer aggregates contributed most to the overall volume of particles in the 5- and 10-nm CT-GNPs, whereas the CT-GNP-30 and CT-GNP-50 samples did not aggregate. Here, we discuss the potential

  5. Extinction, emission, and scattering spectroscopy of 5-50 nm citrate-coated gold nanoparticles: An argument for curvature effects on aggregation

    NASA Astrophysics Data System (ADS)

    Esfahani, Milad Rabbani; Pallem, Vasanta L.; Stretz, Holly A.; Wells, Martha J. M.

    2017-03-01

    The interaction of macromolecules with gold nanoparticles (GNPs) is of interest in the emerging field of biomedical and environmental detection devices. However, the physicochemical properties, including spectra, of GNPs in aqueous solution in the absence of metal-macromolecular interactions must first be considered before their activity in biological and environmental systems can be understood. The specific objective of this research was to experimentally illuminate the role of nanoparticle core size on the spectral (simultaneous consideration of extinction, emission, and scattering) versus aggregation behaviors of citrate-coated GNPs (CT-GNPs). It is difficult to find in the literature systematic simultaneous presentation of scattering, emission, and extinction spectra, including the UV range, and thus the present work will aid those who would use such particles for spectroscopic related separations or sensors. The spectroscopic behavior of CT-GNPs with different core sizes (5, 10, 30, and 50 nm) was studied in ultra-pure water at pH 6.0-6.5 employing UV-visible extinction, excitation-emission matrix (EEM), resonance Rayleigh scattering, and dynamic light scattering (DLS) spectroscopies. The CT-GNP-5 and CT-GNP-10 samples aggregated, absorbed light, and emitted light. In contrast, the CT-GNP-30 and CT-GNP-50 samples did not aggregate and did not emit light, but scattered light intensely. Multimodal peaks were observed in the intensity-based DLS spectra of CT-GNP-5 and CT-GNP-10 samples. Monomodal peaks in the volume-based DLS spectra overestimated particle diameters by 60% and 30% for the CT-GNP-5 and CT-GNP-10 samples, respectively, but underestimated diameters by 10% and 4% for the CT-GNP-30 and CT-GNP-50 samples. The volume-based DLS spectra indicated that dimer and trimer aggregates contributed most to the overall volume of particles in the 5- and 10-nm CT-GNPs, whereas the CT-GNP-30 and CT-GNP-50 samples did not aggregate. Here, we discuss the potential

  6. Light extinction in the atmosphere

    SciTech Connect

    Laulainen, N.

    1992-06-01

    Atmospheric aerosol particles originating from natural sources, such as volcanos and sulfur-bearing gas emissions from the oceans, and from human sources, such as sulfur emissions from fossil fuel combustion and biomass burning, strongly affect visual air quality and are suspected to significantly affect radiative climate forcing of the planet. During the daytime, aerosols obscure scenic vistas, while at night they diminish our ability to observe stellar objects. Scattering of light is the main means by which aerosols attenuate and redistribute light in the atmosphere and by which aerosols can alter and reduce visibility and potentially modify the energy balance of the planet. Trends and seasonal variability of atmospheric aerosol loading, such as column-integrated light extinction or optical depth, and how they may affect potential climate change have been difficult to quantify because there have been few observations made of important aerosol optical parameters, such as optical depth, over the globe and over time and often these are of uneven quality. To address questions related to possible climate change, there is a pressing need to acquire more high-quality aerosol optical depth data. Extensive deployment of improved solar radiometers over the next few years will provide higher-quality extinction data over a wider variety of locations worldwide. An often overlooked source of turbidity data, however, is available from astronomical observations, particularly stellar photoelectric photometry observations. With the exception of the Project ASTRA articles published almost 20 years ago, few of these data ever appear in the published literature. This paper will review the current status of atmospheric extinction observations, as highlighted by the ASTRA work and augmented by more recent solar radiometry measurements.

  7. Vertical Profiles of Aerosol Volume from High Spectral Resolution Infrared Transmission Measurements: Results

    NASA Technical Reports Server (NTRS)

    Eldering, Annmarie; Kahn, Brian H.; Mills, Franklin P.; Irion, Fredrick W.; Steele, Helen M.; Gunson, Michael R.

    2004-01-01

    The high-resolution infrared absorption spectra of the Atmospheric Trace Molecule Spectroscopy (ATMOS) experiment are utilized to derive vertical profiles of sulfate aerosol volume density and extinction coefficient. Following the eruption of Mt. Pinatubo in June 1991, the ATMOS spectra obtained on three Space Shuttle missions (1992, 1993, and 1994) provide a unique opportunity to study the global stratospheric sulfate aerosol layer shortly after a major volcanic eruption and periodically during the decay phase. Synthetic sulfate aerosol spectra are fit to the observed spectra, and a global fitting inversion routine is used to derive vertical profiles of sulfate aerosol volume density. Vertical profiles of sulfate aerosol volume density for the three missions over portions of the globe are presented, with the peak in aerosol volume density occurring from as low as 10 km (polar latitudes) to as high as 20 km (subtropical latitudes). Derived aerosol volume density is as high as 2-3.5 (mu)m(exp 3) per cubic centimeter +/-10% in 1992, decreasing to 0.2-0.5 (mu)m(exp 3) per cubic centimeter +/-20% in 1994, in agreement with other experiments. Vertical extinction profiles derived from ATMOS are compared with profiles from Improved Stratospheric And Mesospheric Sounder (ISAMS) and Cryogenic Limb Array Etalon Spectrometer (CLAES) that coincide in space and time and show good general agreement. The uncertainty of the ATMOS vertical profiles is similar to CLAES and consistently smaller than ISAMS at similar altitudes.

  8. Method and apparatus for aerosol-particle absorption spectroscopy. [DOE patent application

    SciTech Connect

    Campillo, A.J.; Lin, H.B.

    1981-06-25

    A method and apparatus are described for determining the absorption spectra, and other properties, of aerosol particles. A heating beam source provides a beam of electromagnetic energy which is scanned through the region of the spectrum which is of interest. Particles exposed to the heating beam which have absorption bands within the band width of the heating beam absorb energy from the beam. The particles are also illuminated by light of a wave length such that the light is scattered by the particles. The absorption spectra of the particles can thus be determined from an analysis of the scattered light since the absorption of energy by the particles will affect the way the light is scattered. Preferably the heating beam is modulated to simplify the analysis of the scattered light. In one embodiment the heating beam is intensity modulated so that the scattered light will also be intensity modulated when the particles absorb energy. In another embodiment the heating beam passes through an interferometer and the scattered light reflects the Fourier Transform of the absorption spectra.

  9. Atmospheric aerosol characterization combining multi-wavelength Raman lidar and MAX-DOAS measurements in Gwanjgu

    NASA Astrophysics Data System (ADS)

    Chong, Jihyo; Shin, Dong Ho; Kim, Kwang Chul; Lee, Kwon-Ho; Shin, Sungkyun; Noh, Young M.; Müller, Detlef; Kim, Young J.

    2011-11-01

    Integrated approach has been adopted at the ADvanced Environmental Research Center (ADEMRC), Gwangju Institute of Science and Technology (GIST), Korea for effective monitoring of atmospheric aerosol. Various active and passive optical remote sensing techniques such as multi-wavelength (3β+2α+1δ) Raman LIDAR, sun-photometry, MAX-DOAS, and satellite retrieval have been utilized. This integrated monitoring system approach combined with in-situ surface measurement is to allow better characterization of physical and optical properties of atmospheric aerosol. Information on the vertical distribution and microphysical properties of atmospheric aerosol is important for understanding its transport characteristics as well as radiative effect. The GIST multi-wavelength (3β + 2α+1δ) Raman lidar system can measure vertical profiles of optical properties of atmospheric aerosols such as extinction coefficients at 355 and 532nm, particle backscatter coefficients at 355, 532 and 1064 nm, and depolarization ratio at 532nm. The incomplete overlap between the telescope field-of-view and beam divergence of the transmitting laser significantly affects lidar measurement, resulting in higher uncertainty near the surface where atmospheric aerosols of interest are concentrated. Differential Optical Absorption Spectroscopy (DOAS) technique is applied as a complementary tool for the detection of atmospheric aerosols near the surface. The passive Multi-Axis DOAS (MAX-DOAS) technique uses scattered sunlight as a light source from several viewing directions. Recently developed aerosol retrieval algorithm based on O4 slant column densities (SCDs) measured at UV and visible wavelengths has been utilized to derive aerosol information (e.g., aerosol optical depth (AOD) and aerosol extinction coefficients (AECs)) in the lower troposphere. The aerosol extinction coefficient at 356 nm was retrieved for the 0-1 and 1-2 km layers based on the MAX-DOAS measurements using the retrieval algorithm

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

    NASA Technical Reports Server (NTRS)

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

    1989-01-01

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

  11. A comprehensive evaluation of water uptake on atmospherically relevant mineral surfaces: DRIFT spectroscopy, thermogravimetric analysis and aerosol growth measurements

    NASA Astrophysics Data System (ADS)

    Gustafsson, R. J.; Orlov, A.; Badger, C. L.; Griffiths, P. T.; Cox, R. A.; Lambert, R. M.

    2005-08-01

    The hygroscopicity of mineral aerosol samples has been examined by three independent methods: diffuse reflectance infrared Fourier transform spectroscopy, thermogravimetric analysis and differential mobility analysis. All three methods allow an evaluation of the water coverage of two samples, CaCO3 and Arizona Test dust, as a function of relative humidity. For the first time, a correlation between absolute gravimetric measurements and the other two (indirect) methods has been established. Water uptake isotherms were reliably determined for both solids which at 298 K and 80% relative humidity exhibited similar coverages of ~4 monolayers. However, the behaviour at low relative humidity was markedly different in the two cases, with Arizona Test Dust showing a substantially higher affinity for water in the contact layer. This is understandable in terms of the chemical composition of these two materials. The mobility analysis results are in good accord with field observations and with our own spectroscopic and gravimetric measurements. These findings are of value for an improved understanding of atmospheric chemical processes.

  12. A comprehensive evaluation of water uptake on atmospherically relevant mineral surfaces: DRIFT spectroscopy, thermogravimetric analysis and aerosol growth measurements

    NASA Astrophysics Data System (ADS)

    Gustafsson, R. J.; Orlov, A.; Badger, C. L.; Griffiths, P. T.; Cox, R. A.; Lambert, R. M.

    2005-12-01

    The hygroscopicity of mineral aerosol samples has been examined by three independent methods: diffuse reflectance infrared Fourier transform spectroscopy, thermogravimetric analysis and differential mobility analysis. All three methods allow an evaluation of the water coverage of two samples, CaCO3 and Arizona Test dust, as a function of relative humidity. For the first time, a correlation between absolute gravimetric measurements and the other two (indirect) methods has been established. Water uptake isotherms were reliably determined for both solids which at 298 K and 80% relative humidity exhibited similar coverages of ~4 monolayers. However, the behaviour at low relative humidity was markedly different in the two cases, with Arizona Test Dust showing a substantially higher affinity for water in the contact layer. This is understandable in terms of the chemical composition of these two materials. The mobility analysis results are in good accord with field observations and with our own spectroscopic and gravimetric measurements. These findings are of value for an understanding of atmospheric chemical processes.

  13. SAGE Aerosol Measurements. Volume 2: 1 January - 31 December 1980

    NASA Technical Reports Server (NTRS)

    Mccormick, M. P.

    1986-01-01

    The stratospheric Aerosol and Gas Experiment (SAGE) satellite system, launched on February 18, 1979, provides profiles of aerosol extinction at wavelengths of 1.00 and 0.45 micron, ozone concentration, and nitrogen dioxide concentration. Data taken during sunset events in the form of zonal averages and seasonal averages of the aerosol extinction at 1.00 and 0.45 micron, ratios of the aerosol extinction to the molecular extinction at 1.00 micron, and ratios of the aerosol extinction at 0.45 micron to the aerosol extinction at 1.00 micron are presented. The averages for l980 are shown in tables and in profile and contour plots (as a function of altitude and latitude). In addition, temperature data provided by the National Oceanic and Atmospheric Administration (NOAA) for the time and location of each SAGE measurement are averaged and shown in a similar format.

  14. SAGE II aerosol correlative observations - Profile measurements

    NASA Technical Reports Server (NTRS)

    Osborn, M. T.; Rosen, J. M.; Mccormick, M. P.; Wang, Pi-Huan; Livinfston, J. M.

    1989-01-01

    Profiles of the aerosol extinction measurements from the Stratospheric Aerosol and Gas Experiment (SAGE) II are compared with profiles from five correlative experiments between November 1984 and July 1986. The correlative profiles were derived from six-channel dustsonde measurements and two-wavelength lidar backscatter data. The correlation between the dustsonde- and lidar-derived measurements and the SAGE II data is good, validating the SAGE II lower stratospheric aerosol extinction measurements.

  15. VizieR Online Data Catalog: Atmospheric extinction properties above Mauna Kea (Buton+, 2013)

    NASA Astrophysics Data System (ADS)

    Buton, C.; Copin, Y.; Aldering, G.; Antilogus, P.; Aragon, C.; Bailey, S.; Baltay, C.; Bongard, S.; Canto, A.; Cellier-Holzem, F.; Childress, M.; Chotard, N.; Fakhouri, H. K.; Gangler, E.; Guy, J.; Hsiao, E. Y.; Kerschhaggl, M.; Kowalski, M.; Loken, S.; Nugent, P.; Paech, K.; Pain, R.; Pecontal, E.; Pereira, R.; Perlmutter, S.; Rabinowitz, D.; Rigault, M.; Runge, K.; Scalzo, R.; Smadja, G.; Tao, C.; Thomas, R. C.; Weaver, B. A.; Wu, C.; Nearby Supernova Factory

    2012-10-01

    SNfactory median atmospheric extinction [mag/airmass] and its decomposition into physical components (Ozone, Aerosol optical depth and Aerosol Angstroem exponent) from 3200Å to 10000Å (2Å bins). (2 data files).

  16. Extinctions of life

    NASA Technical Reports Server (NTRS)

    Sepkoski, J. J. Jr; Sepkoski JJ, J. r. (Principal Investigator)

    1988-01-01

    This meeting presentation examines mass extinctions through earth's history. Extinctions are charted for marine families and marine genera. Timing of marine genera extinctions is discussed. Periodicity in extinctions during the Mesozoic and Cenozoic eras is plotted and compared with Paleozoic extinction peaks. The role of extinction in evolution and mankind's role in present extinctions are examined.

  17. Australian Extinctions

    ERIC Educational Resources Information Center

    Science Teacher, 2005

    2005-01-01

    Massive extinctions of animals and the arrival of the first humans in ancient Australia--which occurred 45,000 to 55,000 years ago--may be linked. Researchers at the Carnegie Institution, University of Colorado, Australian National University, and Bates College believe that massive fires set by the first humans may have altered the ecosystem of…

  18. MAX-DOAS Measurements of Nitrogen Dioxide and Aerosol

    NASA Astrophysics Data System (ADS)

    Mendolia, Deanna

    Multi-axis differential optical absorption spectroscopy (MAX-DOAS) was applied to retrieve tropospheric NO2 and aerosol vertical profiles from downtown Toronto, and King City, Ontario during select periods in 2006 - 2010. Linear regression of MAX-DOAS NO2 vertical column density (VCD) versus OMI (satellite) VCD yielded a good correlation (R = 0.88) and MAX-DOAS negative bias of 20%, which was within the reported uncertainty of the MAX-DOAS and OMI VCD. The average regional Toronto VCD (remotely-sensed via MAX-DOAS and OMI) was half of the near-road VCD obtained in-situ (2.4 x 1016 ± 1.2 x 1016 molec/cm2 ). MAX-DOAS measurements of O4 were coupled with radiative transfer modeling to obtain vertical aerosol extinction profiles and aerosol optical depth (AOD). A strong linear agreement was observed between PM 2.5 concentration and aerosol extinction coefficient (R = 0.92), and MAX-DOAS versus sun photometer AOD (slope = 0.94; R= 0.90).

  19. Direct measurements of the optical cross sections and refractive indices of individual volatile and hygroscopic aerosol particles.

    PubMed

    Mason, B J; Cotterell, M I; Preston, T C; Orr-Ewing, A J; Reid, J P

    2015-06-04

    We present measurements of the evolving extinction cross sections of individual aerosol particles (spanning 700-2500 nm in radius) during the evaporation of volatile components or hygroscopic growth using a combination of a single particle trap formed from a Bessel light beam and cavity ring-down spectroscopy. For single component organic aerosol droplets of 1,2,6-hexanetriol, polyethylene glycol 400, and glycerol, the slow evaporation of the organic component (over time scales of 1000 to 10,000 s) leads to a time-varying size and extinction cross section that can be used to estimate the refractive index of the droplet. Measurements on binary aqueous-inorganic aerosol droplets containing one of the inorganic solutes ammonium bisulfate, ammonium sulfate, sodium nitrate, or sodium chloride (over time scales of 1000 to 15,000 s) under conditions of changing relative humidity show that extinction cross-section measurements are consistent with expectations from accepted models for the variation in droplet refractive index with hygroscopic growth. In addition, we use these systems to establish an experimental protocol for future single particle extinction measurements. The advantages of mapping out the evolving light extinction cross-section of an individual particle over extended time frames accompanied by hygroscopic cycling or component evaporation are discussed.

  20. Primary and secondary biomass burning aerosols determined by proton nuclear magnetic resonance (1H-NMR) spectroscopy during the 2008 EUCAARI campaign in the Po Valley (Italy)

    NASA Astrophysics Data System (ADS)

    Paglione, M.; Saarikoski, S.; Carbone, S.; Hillamo, R.; Facchini, M. C.; Finessi, E.; Giulianelli, L.; Carbone, C.; Fuzzi, S.; Moretti, F.; Tagliavini, E.; Swietlicki, E.; Eriksson Stenström, K.; Prévôt, A. S. H.; Massoli, P.; Canaragatna, M.; Worsnop, D.; Decesari, S.

    2014-05-01

    Atmospheric organic aerosols are generally classified as primary and secondary (POA and SOA) according to their formation processes. An actual separation, however, is challenging when the timescales of emission and gas-to-particle formation overlap. The presence of SOA formation in biomass burning plumes leads to scientific questions about whether the oxidized fraction of biomass burning aerosol is rather of secondary or primary origin, as some studies would suggest, and about the chemical compositions of oxidized biomass burning POA and SOA. In this study, we apply nuclear magnetic resonance (NMR) spectroscopy to investigate the functional group composition of fresh and aged biomass burning aerosols during an intensive field campaign in the Po Valley, Italy. The campaign was part of the EUCAARI project and was held at the rural station of San Pietro Capofiume in spring 2008. Factor analysis applied to the set of NMR spectra was used to apportion the wood burning contribution and other organic carbon (OC) source contributions, including aliphatic amines. Our NMR results, referred to the polar, water-soluble fraction of OC, show that fresh wood burning particles are composed of polyols and aromatic compounds, with a sharp resemblance to wood burning POA produced in wood stoves, while aged samples are clearly depleted of alcohols and are enriched in aliphatic acids with a smaller contribution of aromatic compounds. The comparison with biomass burning organic aerosols (BBOA) determined by high-resolution aerosol mass spectrometry (HR-TOF-AMS) at the site shows only a partial overlap between NMR BB-POA and AMS BBOA, which can be explained by either the inability of BBOA to capture all BB-POA composition, especially the alcohol fraction, or the fact that BBOA account for insoluble organic compounds unmeasured by the NMR. Therefore, an unambiguous composition for biomass burning POA could not be derived from this study, with NMR analysis indicating a higher O / C ratio

  1. Primary and secondary biomass burning aerosols determined by proton nuclear magnetic resonance (H-NMR) spectroscopy during the 2008 EUCAARI campaign in the Po Valley (Italy)

    NASA Astrophysics Data System (ADS)

    Paglione, M.; Saarikoski, S.; Carbone, S.; Hillamo, R.; Facchini, M. C.; Finessi, E.; Giulianelli, L.; Carbone, C.; Fuzzi, S.; Moretti, F.; Tagliavini, E.; Swietlicki, E.; Eriksson Stenström, K.; Prévôt, A. S. H.; Massoli, P.; Canaragatna, M.; Worsnop, D.; Decesari, S.

    2013-12-01

    Atmospheric organic aerosols are generally classified into primary and secondary (POA and SOA) according to their formation processes. An actual separation, however, is challenging when the timescales of emission and of gas-to-particle formation overlap. The presence of SOA formation in biomass burning plumes leads to scientific questions about whether the oxidized fraction of biomass burning aerosol is rather of secondary or primary origin, as some studies would suggest, and about the chemical compositions of oxidized biomass burning POA and SOA. In this study, we apply nuclear magnetic resonance (NMR) spectroscopy to investigate the functional group composition of fresh and aged biomass burning aerosols during an intensive field campaign in the Po Valley, Italy. The campaign was part of the EUCAARI project and was held at the rural station of San Pietro Capofiume in spring 2008. Factor analysis applied to the set of NMR spectra was used to apportion the wood burning contribution and other organic carbon (OC) source contributions, including aliphatic amines. Our NMR results, referred to the polar, water-soluble fraction of OC, show that fresh wood burning particles are composed of polyols and aromatic compounds, with a sharp resemblance with wood burning POA produced in wood stoves, while aged samples are clearly depleted of alcohols and are enriched in aliphatic acids with a smaller contribution of aromatic compounds. The comparison with biomass burning organic aerosols (BBOA) determined by high resolution aerosol mass spectrometry (HR-TOF-AMS) at the site shows only a partial overlap between NMR BB-POA and AMS BBOA, which can be explained by either the inability of BBOA to capture all BB-POA composition, especially the alcohol fraction, or the fact that BBOA account for insoluble organic compounds unmeasured by the NMR. Therefore, an unambiguous composition for biomass burning POA could not be derived from this study, with NMR analysis indicating a higher O / C

  2. DUST EXTINCTION FROM BALMER DECREMENTS OF STAR-FORMING GALAXIES AT 0.75 {<=} z {<=} 1.5 WITH HUBBLE SPACE TELESCOPE/WIDE-FIELD-CAMERA 3 SPECTROSCOPY FROM THE WFC3 INFRARED SPECTROSCOPIC PARALLEL SURVEY

    SciTech Connect

    Dominguez, A.; Siana, B.; Masters, D.; Henry, A. L.; Martin, C. L.; Scarlata, C.; Bedregal, A. G.; Malkan, M.; Ross, N. R.; Atek, H.; Colbert, J. W.; Teplitz, H. I.; Rafelski, M.; McCarthy, P.; Hathi, N. P.; Dressler, A.; Bunker, A.

    2013-02-15

    Spectroscopic observations of H{alpha} and H{beta} emission lines of 128 star-forming galaxies in the redshift range 0.75 {<=} z {<=} 1.5 are presented. These data were taken with slitless spectroscopy using the G102 and G141 grisms of the Wide-Field-Camera 3 (WFC3) on board the Hubble Space Telescope as part of the WFC3 Infrared Spectroscopic Parallel survey. Interstellar dust extinction is measured from stacked spectra that cover the Balmer decrement (H{alpha}/H{beta}). We present dust extinction as a function of H{alpha} luminosity (down to 3 Multiplication-Sign 10{sup 41} erg s{sup -1}), galaxy stellar mass (reaching 4 Multiplication-Sign 10{sup 8} M {sub Sun }), and rest-frame H{alpha} equivalent width. The faintest galaxies are two times fainter in H{alpha} luminosity than galaxies previously studied at z {approx} 1.5. An evolution is observed where galaxies of the same H{alpha} luminosity have lower extinction at higher redshifts, whereas no evolution is found within our error bars with stellar mass. The lower H{alpha} luminosity galaxies in our sample are found to be consistent with no dust extinction. We find an anti-correlation of the [O III] {lambda}5007/H{alpha} flux ratio as a function of luminosity where galaxies with L {sub H{alpha}} < 5 Multiplication-Sign 10{sup 41} erg s{sup -1} are brighter in [O III] {lambda}5007 than H{alpha}. This trend is evident even after extinction correction, suggesting that the increased [O III] {lambda}5007/H{alpha} ratio in low-luminosity galaxies is likely due to lower metallicity and/or higher ionization parameters.

  3. Measuring black carbon spectral extinction in the visible and infrared

    NASA Astrophysics Data System (ADS)

    Smith, A. J. A.; Peters, D. M.; McPheat, R.; Lukanihins, S.; Grainger, R. G.

    2015-09-01

    This work presents measurements of the spectral extinction of black carbon aerosol from 400 nm to 15 μm. The aerosol was generated using a Miniature Combustion Aerosol Standard soot generator and then allowed to circulate in an aerosol cell where its extinction was measured using a grating spectrometer in the visible and a Fourier transform spectrometer in the infrared. Size distribution, number concentration, and mass extinction cross sections have also been obtained using single-particle aerosol samplers. A mean mass extinction cross section at 550 nm of 8.3 ± 1.6 m2 g-1 is found which, assuming a reasonable single scatter albedo of 0.2, corresponds to a mass absorption cross section of 6.6 ± 1.3 m2 g-1. This compares well with previously reported literature values. Computer analysis of electron microscope images of the particles provides independent confirmation of the size distribution as well as fractal parameters of the black carbon aerosol. The aerosol properties presented in this work are representative of very fresh, uncoated black carbon aerosol. After atmospheric processing of such aerosols (which could include mixing with other constituents and structural changes), different optical properties would be expected.

  4. Measured Infrared Optical Cross Sections For a Variety Of Chemical and Biological Aerosol Simulants

    NASA Astrophysics Data System (ADS)

    Gurton, Kristan P.; Ligon, David; Dahmani, Rachid

    2004-08-01

    We conducted a series of spectral extinction measurements on a variety of aerosolized chemical and biological simulants over the spectral range 3-13 µm using conventional Fourier-transform IR (FTIR) aerosol spectroscopy. Samples consist of both aerosolized particulates and atomized liquids. Materials considered include Bacillus subtilis endospores, lyophilized ovalbumin, polyethylene glycol, dimethicone (SF-96), and three common background materials: kaolin clay (hydrated aluminum silicate), Arizona road dust (primarily SiO2), and diesel soot. Aerosol size distributions and mass density were measured simultaneously with the FTIR spectra. As a result, all optical parameters presented here are mass normalized, i.e., in square meters per gram. In an effort to establish the utility of using Mie theory to predict such parameters, we conducted a series of calculations. For materials in which the complex indices of refraction are known, e.g., silicone oil (SF-96) and kaolin, measured size distributions were convolved with Mie theory and the resultant spectral extinction calculated. Where there was good agreement between measured and calculated extinction spectra, absorption, total scattering, and backscatter were also calculated.

  5. The application of accelerator mass spectroscopy (AMS) in the study of source identification of aerosols in China

    SciTech Connect

    Shao Min; Tang Xiaoyan; Li Jinlong

    1995-12-01

    Accelerator Mass Spectrometry is a new physical technique and it was successfully established in China in 1992. This paper tried to apply the AMS in source identification for atmospheric aerosols which was part of our national project of AMS application in environmental research. For comparison, we also studied the aerosol sources by multivariate analysis models such as correspond factor analysis, principal factor analysis and target recognition analysis. For the samples we collected in suburb of Beijing, the results by factor analysis showed that the predominant TSP source was soil which contributed more than 50% to atmospheric particles. However, the AMS results demonstrated that carbonaceous aerosols have quite different emission sources. For carbonaceous aerosols of Beijing, Hunan and Shandong, the contribution to ambient particles from fossil fuel was nearly 2/3, and as the man-made activities (coal-burning, etc.) increased, the fossil part contributed more. Therefore, it`s significant to combine the method of factor analysis and AMS in the study of atmospheric aerosols.

  6. Interstellar Extinction

    NASA Astrophysics Data System (ADS)

    Gontcharov, G. A.

    2016-12-01

    This review describes our current understanding of interstellar extinction. This differ substantially from the ideas of the 20th century. With infrared surveys of hundreds of millions of stars over the entire sky, such as 2MASS, SPITZER-IRAC, and WISE, we have looked at the densest and most rarefied regions of the interstellar medium at distances of a few kpc from the Sun. Observations at infrared and microwave wavelengths, where the bulk of the interstellar dust absorbs and radiates, have brought us closer to an understanding of the distribution of the dust particles on scales of the Galaxy and the universe. We are in the midst of a scientific revolution in our understanding of the interstellar medium and dust. Progress in, and the key results of, this revolution are still difficult to predict. Nevertheless, (a) a physically justified model has been developed for the spatial distribution of absorbing material over the nearest few kiloparsecs, including the Gould belt as a dust container, which gives an accurate estimate of the extinction for any object just by its galactic coordinates. It is also clear that (b) the interstellar medium contains roughly half the mass of matter in the galactic vicinity of the solar system (the other half is made up of stars, their remnants, and dark matter) and (c) the interstellar medium and, especially, dust, differ substantially in different regions of space and deep space cannot be understood by only studying near space.

  7. Impossible Extinction

    NASA Astrophysics Data System (ADS)

    Cockell, Charles S.

    2003-03-01

    Every 225 million years the Earth, and all the life on it, completes one revolution around the Milky Way Galaxy. During this remarkable journey, life is influenced by calamitous changes. Comets and asteroids strike the surface of the Earth, stars explode, enormous volcanoes erupt, and, more recently, humans litter the planet with waste. Many animals and plants become extinct during the voyage, but humble microbes, simple creatures made of a single cell, survive this journey. This book takes a tour of the microbial world, from the coldest and deepest places on Earth to the hottest and highest, and witnesses some of the most catastrophic events that life can face. Impossible Extinction tells this remarkable story to the general reader by explaining how microbes have survived on Earth for over three billion years. Charles Cockell received his doctorate from the University of Oxford, and is currently a microbiologist with rhe Search for Extraterrestrial Intelligence Institute (SETI), based at the British Antarctic Survey in Cambridge, UK. His research focusses on astrobiology, life in the extremes and the human exploration of Mars. Cockell has been on expeditions to the Arctic, Antarctic, Mongolia, and in 1993 he piloted a modified insect-collecting ultra-light aircraft over the Indonesian rainforests. He is Chair of the Twenty-one Eleven Foundation for Exploration, a charity that supports expeditions that forge links between space exploration and environmentalism.

  8. Large Binocular Telescope and Sptizer Spectroscopy of Star-forming Galaxies at 1 < z < 3: Extinction and Star Formation Rate Indicators

    NASA Technical Reports Server (NTRS)

    Rujopakarn, W.; Rieke, G. H.; Papovich, C. J.; Weiner, B. J.; Rigby, Jane; Rex, M.; Bian, F.; Kuhn, O. P.; Thompson, D.

    2012-01-01

    We present spectroscopic observations in the rest-frame optical and near- to mid-infrared wavelengths of four gravitationally lensed infrared (IR) luminous star-forming galaxies at redshift 1 < z < 3 from the LUCIFER instrument on the Large Binocular Telescope and the Infrared Spectrograph on Spitzer. The sample was selected to represent pure, actively star-forming systems, absent of active galactic nuclei. The large lensing magnifications result in high signal-to-noise spectra that can probe faint IR recombination lines, including Paa and Bra at high redshifts. The sample was augmented by three lensed galaxies with similar suites of unpublished data and observations from the literature, resulting in the final sample of seven galaxies. We use the IR recombination lines in conjunction with Ha observations to probe the extinction, Av, of these systems, as well as testing star formation rate (SFR) indicators against the SFR measured by fitting spectral energy distributions to far-IR photometry. Our galaxies occupy a range of Av from 0 to 5.9 mag, larger than previously known for a similar range of IR luminosities at these redshifts. Thus, estimates of SFR even at z 2 must take careful count of extinction in the most IR luminous galaxies.We also measure extinction by comparing SFR estimates from optical emission lines with those from far- IR measurements. The comparison of results from these two independent methods indicates a large variety of dust distribution scenarios at 1 < z < 3. Without correcting for dust extinction, the Ha SFR indicator underestimates the SFR; the size of the necessary correction depends on the IR luminosity and dust distribution scenario. Individual SFR estimates based on the 6.2µm polycyclic aromatic hydrocarbon emission line luminosity do not show a systematic discrepancy with extinction, although a considerable, 0.2 dex, scatter is observed.

  9. Infrared differential-absorption Mueller matrix spectroscopy and neural network-based data fusion for biological aerosol standoff detection.

    PubMed

    Carrieri, Arthur H; Copper, Jack; Owens, David J; Roese, Erik S; Bottiger, Jerold R; Everly, Robert D; Hung, Kevin C

    2010-01-20

    An active spectrophotopolarimeter sensor and support system were developed for a military/civilian defense feasibility study concerning the identification and standoff detection of biological aerosols. Plumes of warfare agent surrogates gamma-irradiated Bacillus subtilis and chicken egg white albumen (analytes), Arizona road dust (terrestrial interferent), water mist (atmospheric interferent), and talcum powders (experiment controls) were dispersed inside windowless chambers and interrogated by multiple CO(2) laser beams spanning 9.1-12.0 microm wavelengths (lambda). Molecular vibration and vibration-rotation activities by the subject analyte are fundamentally strong within this "fingerprint" middle infrared spectral region. Distinct polarization-modulations of incident irradiance and backscatter radiance of tuned beams generate the Mueller matrix (M) of subject aerosol. Strings of all 15 normalized elements {M(ij)(lambda)/M(11)(lambda)}, which completely describe physical and geometric attributes of the aerosol particles, are input fields for training hybrid Kohonen self-organizing map feed-forward artificial neural networks (ANNs). The properly trained and validated ANN model performs pattern recognition and type-classification tasks via internal mappings. A typical ANN that mathematically clusters analyte, interferent, and control aerosols with nil overlap of species is illustrated, including sensitivity analysis of performance.

  10. Influence of oxygen addition to the carrier gas on laser-induced breakdown spectroscopy measurements on aerosols

    NASA Astrophysics Data System (ADS)

    Palazzo, N.; Migliorini, F.; Dondè, R.; Maffi, S.; De Iuliis, S.

    2016-01-01

    In this work, laser-induced breakdown spectrosopy is implemented on aerosol particles for absolute concentration analysis. The aim of this work is the investigation of the effect of the bath gas used for nebulizing the aerosol. Nitrogen, air, and 50% O2 in N2 mixture have been chosen as carrier gasses in order to analyze the effect of oxygen addition to the gas. LIBS measurements have been carried out on aerosol particles produced from CuCl2 2H2O solutions, and the 324.7 nm Cu line is considered. As a first analysis, plasma parameters, such as temperature and electron density, have been evaluated changing the carrier gas. Measurements to derive the LIBS calibration curve of the 324.7 nm Cu line are carried out in air and in N2. The significant difference in the slope of the resulting calibration curves has to be attributed to the oxygen addition to the bath gas. To explore such behavior, time-resolved measurements of the Cu line and peak/base ratio have been performed. The presence of two competitive effects have been observed that becomes significant increasing the amount of oxygen in the carrier gas. One is the oxygen-quenching effect, already observed in the literature, and the other one is the enhancement of the Cu LIBS signal, expecially at short delay times. These effects have been observed also at other Cu lines and changing the analyte source. The results are presented and widely discussed.

  11. Asian Aerosols: A Geophysical Fluid Dynamics Laboratory general circulation model sensitivity study of model response to aerosol optical depth and aerosol absorption

    NASA Astrophysics Data System (ADS)

    Randles, C. A.; Ramaswamy, V.

    2007-12-01

    Atmospheric absorption by black carbon (BC) aerosol heats the atmosphere while simultaneously cooling the surface and reducing latent and sensible heat fluxes from the land. Recent studies have shown that absorbing BC aerosol can have a large impact on regional climates, including modification of the hydrological cycle. However, significant uncertainties remain with regards to (a) the total amount of all aerosol species and (b) the amount of aerosol absorption. Here we present a GCM sensitivity study focusing on the influences due to total aerosol amount and aerosol absorption in the south and east Asian regions. Six experiments are conducted to test the equilibrium response of the GFDL AM2 GCM (under conditions of prescribed, observed sea surface temperatures) to (i) changes in aerosol absorption caused by changes in BC aerosol amount, and (ii) aerosol extinction optical depth increases corresponding to the year 1990 relative to a control case of 1950. In order to systematically explore the uncertainties in aerosol loading and absorption, the sensitivity experiments are classified into four regimes: low extinction optical depth, low absorption; low extinction optical depth, high absorption; high extinction optical depth, low absorption; and high extinction optical depth, high absorption. Changes in surface temperature and changes in the hydrological cycle are generally insignificant when lower aerosol extinction optical depths are considered. For higher extinction optical depths, the change in the modeled regional circulation relative to the control circulation over south and east Asia is affected by the amount of aerosol absorption and contrasts sharply to the regional circulation change associated with increasing only scattering aerosols. When increasing absorbing aerosols over the region, low-level convergence and increases in vertical velocity overcome the stabilizing effects of the absorbing aerosol and enhance the monsoonal circulation and precipitation rate

  12. Hygroscopicity of Early Earth and Titan Laboratory Aerosol Analogs

    NASA Astrophysics Data System (ADS)

    Hasenkopf, C. A.; Beaver, M. R.; Freedman, M. A.; Toon, O. B.; Tolbert, M. A.

    2009-12-01

    We have explored the ability of organic hazes, known to exist in the atmosphere of Titan and postulated to have existed in the Archean Earth atmosphere, to act as cloud condensation nuclei (CCN). These laboratory aerosol analogs are generated via UV-photolysis of early Earth and Titan analog gas mixtures and are designed to mimic the present day atmospheric conditions on Titan and the early Earth atmosphere before the rise of oxygen. Water uptake is observed to occur on the early Earth and Titan aerosol analogs at relative humidities of 80% - 90% via optical growth measurements using cavity ring-down aerosol extinction spectroscopy. We find the optical growth of these aerosols is similar to known slightly-soluble organic acids, such as phthalic and pyromellitic acids. On average, the optical growth of the early Earth analog is slightly larger than the Titan analog. In order to translate our measurements obtained in a subsaturated regime into the CCN ability of these particles, we rely on the hygroscopicity parameter κ, developed by Petters & Kreidenweis (2007). We retrieve κ = 0.17±0.03 and 0.06±0.01 for the early Earth and Titan analogs, respectively. This early Earth analog hygroscopicity value indicates that the aerosol could activate at reasonable water vapor supersaturations. We use previous aerosol mass spectrometry results to correlate the chemical structure of the two types of analog with their hygroscopicity. The hygroscopicity of the early Earth aerosol analog, coupled with the apparent lack of other good CCN during the Archean, helps explain the role of the organic haze in the indirect effect of clouds on the early Earth and indicates that it may have had a significant impact on the hydrological cycle.

  13. A case study of dust aerosol radiative properties over Lanzhou, China

    NASA Astrophysics Data System (ADS)

    Zhang, L.; Cao, X.; Bao, J.; Zhou, B.; Huang, J.; Shi, J.; Bi, J.

    2010-02-01

    The vertical distribution of dust aerosol and its radiative properties are analysed using the data measured by the micropulse lidar, profiling microwave radiometer, sunphotometer, particulate monitor, and nephelometer at the Semi-Arid Climate and Environment Observatory of Lanzhou University (SACOL) during a dust storm from 27 March to 29 March 2007. The analysis shows that the dust aerosol mainly exists below 2 km in height, and the dust aerosol extinction coefficient decreases with height. The temporal evolution of aerosol optical depth (AOD) during the dust storm is characterized by a sub-maximum at 22:00 (Beijing Time) on 27 March and a maximum at 12:00 on 28 March. The AOD derived by lidar is compared with that obtained by sunphotometer, and shows a good consistency. The PM10 concentration and aerosol scattering coefficient share identical variation trends, and their maximums both appear at 22:00 on 27 March. The aerosol extinction coefficient and relative humidity have the same trends and their maximums appear at identical heights, showing a correlation between extinction coefficient and relative humidity known as aerosol hygroscopicity. Nevertheless, the correlation between aerosol extinction coefficient and temperature cannot be obviously seen. The aerosol extinction coefficient, scattering coefficient, and PM10 concentration present good linear correlations. The correlation coefficients of the aerosol scattering coefficient and PM10 concentration, of aerosol extinction coefficient and PM10 concentration, and of aerosol extinction and scattering coefficient are respectively 0.98, 0.94, and 0.96.

  14. Radiative Effects of Aerosols

    NASA Technical Reports Server (NTRS)

    Valero, Francisco P. J.

    1996-01-01

    During the Atlantic Stratocumulus Transition Experiment (ASTEX) in June 1992, two descents in cloud-free regions allowed comparison of the change in aerosol optical depth as determined by an onboard total-direct-diffuse radiometer (TDDR) to the change calculated from measured size-resolved aerosol microphysics and chemistry. Both profiles included a pollution haze from Europe but the second also included the effect of a Saharan dust layer above the haze. The separate contributions of supermicrometer (coarse) and submicrometer (fine) aerosol were determined and thermal analysis of the pollution haze indicated that the fine aerosol was composed primarily of a sulfate/water mixture with a refractory soot-like core. The soot core increased the calculated extinction by about 10% in the most polluted drier layer relative to a pure sulfate aerosol but had significantly less effect at higher humidities. A 3 km descent through a boundary layer air mass dominated by pollutant aerosol with relative humidities (RH) 10-77% yielded a close agreement between the measured and calculated aerosol optical depths (550 nm) of 0.160 (+/- 0.07) and 0. 157 (+/- 0.034) respectively. During descent the aerosol mass scattering coefficient per unit sulfate mass varied from about 5 to 16 m(exp 2)/g and primarily dependent upon ambient RH. However, the total scattering coefficient per total fine mass was far less variable at about 4+/- 0.7 m(exp 2)/g. A subsequent descent through a Saharan dust layer located above the pollution aerosol layer revealed that both layers contributed similarly to aerosol optical depth. The scattering per unit mass of the coarse aged dust was estimated at 1.1 +/- 0.2 m(exp 2)/g. The large difference (50%) in measured and calculated optical depth for the dust layer exceeded measurements.

  15. Heterogeneous interaction of SiO2 with N2O5: aerosol flow tube and single particle optical levitation-Raman spectroscopy studies.

    PubMed

    Tang, M J; Camp, J C J; Rkiouak, L; McGregor, J; Watson, I M; Cox, R A; Kalberer, M; Ward, A D; Pope, F D

    2014-09-25

    Silica (SiO2) is an important mineral present in atmospheric mineral dust particles, and the heterogeneous reaction of N2O5 on atmospheric aerosol is one of the major pathways to remove nitrogen oxides from the atmosphere. The heterogeneous reaction of N2O5 with SiO2 has only been investigated by two studies previously, and the reported uptake coefficients differ by a factor of >10. In this work two complementary laboratory techniques were used to study the heterogeneous reaction of SiO2 particles with N2O5 at room temperature and at different relative humidities (RHs). The uptake coefficients of N2O5, γ(N2O5), were determined to be (7.2 ± 0.6) × 10(-3) (1σ) at 7% RH and (5.3 ± 0.8) × 10(-3) (1σ) at 40% RH for SiO2 particles, using the aerosol flow tube technique. We show that γ(N2O5) determined in this work can be reconciled with the two previous studies by accounting for the difference in geometric and BET derived aerosol surface areas. To probe the particle phase chemistry, individual micrometer sized SiO2 particles were optically levitated and exposed to a continuous flow of N2O5 at different RHs, and the composition of levitated particles was monitored online using Raman spectroscopy. This study represents the first investigation into the heterogeneous reactions of levitated individual SiO2 particles as a surrogate for mineral dust. Relative humidity was found to play a critical role: while no significant change of particle composition was observed by Raman spectroscopy during exposure to N2O5 at RH of <2%, increasing the RH led to the formation of nitrate species on the particle surface which could be completely removed after decreasing the RH back to <2%. This can be explained by the partitioning of HNO3 between the gas and adsorbed phases. The atmospheric implications of this work are discussed.

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

    NASA Technical Reports Server (NTRS)

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

    1989-01-01

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

  17. Airborne Aerosol Closure Studies During PRIDE

    NASA Technical Reports Server (NTRS)

    Redemann, Jens; Livingston, John M.; Russell, Philip B.; Schmid, Beat; Reid, Jeff

    2000-01-01

    The Puerto Rico Dust Experiment (PRIDE) was conducted during June/July of 2000 to study the properties of Saharan dust aerosols transported across the Atlantic Ocean to the Caribbean Islands. During PRIDE, the NASA Ames Research Center six-channel (380 - 1020 nm) airborne autotracking sunphotometer (AATS-6) was operated aboard a Piper Navajo airplane alongside a suite of in situ aerosol instruments. The in situ aerosol instrumentation relevant to this paper included a Forward Scattering Spectrometer Probe (FSSP-100) and a Passive Cavity Aerosol Spectrometer Probe (PCASP), covering the radius range of approx. 0.05 to 10 microns. The simultaneous and collocated measurement of multi-spectral aerosol optical depth and in situ particle size distribution data permits a variety of closure studies. For example, vertical profiles of aerosol optical depth obtained during local aircraft ascents and descents can be differentiated with respect to altitude and compared to extinction profiles calculated using the in situ particle size distribution data (and reasonable estimates of the aerosol index of refraction). Additionally, aerosol extinction (optical depth) spectra can be inverted to retrieve estimates of the particle size distributions, which can be compared directly to the in situ size distributions. In this paper we will report on such closure studies using data from a select number of vertical profiles at Cabras Island, Puerto Rico, including measurements in distinct Saharan Dust Layers. Preliminary results show good agreement to within 30% between mid-visible aerosol extinction derived from the AATS-6 optical depth profiles and extinction profiles forward calculated using 60s-average in situ particle size distributions and standard Saharan dust aerosol refractive indices published in the literature. In agreement with tendencies observed in previous studies, our initial results show an underestimate of aerosol extinction calculated based on the in situ size distributions

  18. Quality Screening Algorithms Implemented in the New CALIPSO Level 3 Aerosol Profile Product

    NASA Astrophysics Data System (ADS)

    Tackett, J. L.; Winker, D. M.; Getzewich, B. J.; Vaughan, M.

    2012-12-01

    Global observations of aerosol extinction profiles can improve the ability of climate models to properly account for aerosol radiative forcing in Earth's atmosphere. In response to this need, a new CALIPSO (Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observations) level 3 aerosol profile product has been released which for the first time provides monthly, globally gridded and quality-screened aerosol extinction profiles within the troposphere for the entire 6-year mission. Level 3 aerosol extinction profiles are aggregated from CALIOP (Cloud-Aerosol Lidar with Orthogonal Polarization) lidar extinction retrievals reported in the CALIPSO level 2 aerosol profile product onto an equal-angle grid after quality screening algorithms are applied to reduce occurrences of failed retrievals, misclassified aerosol, surface contamination, and spurious outliers. Implementation of these quality screening algorithms is a substantial value to aerosol modeling groups who desire high confidence datasets without having to independently develop quality screening metrics. Furthermore, quality screening is paramount to understand the scientific content of the resultant CALIPSO level 3 aerosol profile product since classification and retrieval errors in level 2 aerosol data may lead to misinterpretation of the distribution and optical properties of aerosol in the troposphere. This presentation summarizes the averaging and quality screening algorithms implemented in the CALIPSO level 3 aerosol profile product, provides rationale for their implementation, and discusses averaging and filtering differences unique to CALIPSO data compared to level 3 products aggregated from passive satellite measurements. Examples are given that illustrate the benefits of quality screening and the dangers of improper screening CALIPSO level 2 aerosol extinction data. Sensitivity study results are presented to highlight the impact of quality screening on final level 3 statistics. Since overlying cloud

  19. The nature of extinction.

    PubMed

    Delord, Julien

    2007-09-01

    The phenomenon of species extinction raises more and more concern among ecologists facing the actual crisis of biodiversity. Scientific investigations of the causes and effects of extinction must be completed by a philosophical analysis of the concept of extinction that aims to clarify the meanings of the term 'extinction' and to analyse modalities, criteria and degrees of extinction. We will focus our attention on the apparent paradox of the possible 'resurrection' of species in the near future with the help of genetic biotechnology and cloning techniques. The ontological background of the extinction concept is analysed in relation to the idea of species as classes. We will also show that there is no simple analogy between death and species extinction, and develop a conceptualist and dualistic system of supra-individual entities (species vs. population), supported by an instrumentalist approach to genetic manipulations which transform species into interactive kinds, which can go extinct and be recreated.

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

    NASA Technical Reports Server (NTRS)

    1976-01-01

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

  1. Is extinction forever?

    PubMed Central

    Bridge, Eli S.; Crawford, Priscilla H. C.; Hough, Daniel J.; Kelly, Jeffrey F.; Patten, Michael A.

    2015-01-01

    Mistrust of science has seeped into public perception of the most fundamental aspect of conservation—extinction. The term ought to be straightforward, and yet, there is a disconnect between scientific discussion and public views. This is not a mere semantic issue, rather one of communication. Within a population dynamics context, we say that a species went locally extinct, later to document its return. Conveying our findings matters, for when we use local extinction, an essentially nonsensical phrase, rather than extirpation, which is what is meant, then we contribute to, if not create outright, a problem for public understanding of conservation, particularly as local extinction is often shortened to extinction in media sources. The public that receives the message of our research void of context and modifiers comes away with the idea that extinction is not forever or, worse for conservation as a whole, that an extinction crisis has been invented. PMID:25711479

  2. Stratospheric aerosol forcing for climate modeling: 1850-1978

    NASA Astrophysics Data System (ADS)

    Arfeuille, Florian; Luo, Beiping; Thomason, Larry; Vernier, Jean-Paul; Peter, Thomas

    2016-04-01

    We present here a stratospheric aerosol dataset produced using the available aerosol optical depth observations from the pre-satellite period. The scarce atmospheric observations are supplemented by additional information from an aerosol microphysical model, initialized by ice-core derived sulfur emissions. The model is used to derive extinctions at all altitudes, latitudes and times when sulfur injections are known for specific volcanic eruptions. The simulated extinction coefficients are then scaled to match the observed optical depths. In order to produce the complete optical properties at all wavelengths (and the aerosol surface area and volume densities) needed by climate models, we assume a lognormal size distribution of the aerosols. Correlations between the extinctions in the visible and the effective radius and distribution width parameters are taken from the better constrained SAGE II period. The aerosol number densities are then fitted to match the derived extinctions in the 1850-1978 period. From these aerosol size distributions, we then calculate extinction coefficients, single scattering albedos and asymmetry factors at all wavelengths using the Mie theory. The aerosol surface area densities and volume densities are also provided.

  3. Stratospheric Aerosol Measurements

    NASA Technical Reports Server (NTRS)

    Pueschel, Rudolf, F.; Gore, Warren J. (Technical Monitor)

    1998-01-01

    Stratospheric aerosols affect the atmospheric energy balance by scattering and absorbing solar and terrestrial radiation. They also can alter stratospheric chemical cycles by catalyzing heterogeneous reactions which markedly perturb odd nitrogen, chlorine and ozone levels. Aerosol measurements by satellites began in NASA in 1975 with the Stratospheric Aerosol Measurement (SAM) program, to be followed by the Stratospheric Aerosol and Gas Experiment (SAGE) starting in 1979. Both programs employ the solar occultation, or Earth limb extinction, techniques. Major results of these activities include the discovery of polar stratospheric clouds (PSCs) in both hemispheres in winter, illustrations of the impacts of major (El Chichon 1982 and Pinatubo 1991) eruptions, and detection of a negative global trend in lower stratospheric/upper tropospheric aerosol extinction. This latter result can be considered a triumph of successful worldwide sulfur emission controls. The SAGE record will be continued and improved by SAGE III, currently scheduled for multiple launches beginning in 2000 as part of the Earth Observing System (EOS). The satellite program has been supplemented by in situ measurements aboard the ER-2 (20 km ceiling) since 1974, and from the DC-8 (13 km ceiling) aircraft beginning in 1989. Collection by wire impactors and subsequent electron microscopic and X-ray energy-dispersive analyses, and optical particle spectrometry have been the principle techniques. Major findings are: (1) The stratospheric background aerosol consists of dilute sulfuric acid droplets of around 0.1 micrometer modal diameter at concentration of tens to hundreds of monograms per cubic meter; (2) Soot from aircraft amounts to a fraction of one percent of the background total aerosol; (3) Volcanic eruptions perturb the sulfuric acid, but not the soot, aerosol abundance by several orders of magnitude; (4) PSCs contain nitric acid at temperatures below 195K, supporting chemical hypotheses

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

    NASA Technical Reports Server (NTRS)

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

    1986-01-01

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

  5. 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.

  6. Secondary extinctions of biodiversity.

    PubMed

    Brodie, Jedediah F; Aslan, Clare E; Rogers, Haldre S; Redford, Kent H; Maron, John L; Bronstein, Judith L; Groves, Craig R

    2014-12-01

    Extinctions beget further extinctions when species lose obligate mutualists, predators, prey, or hosts. Here, we develop a conceptual model of species and community attributes affecting secondary extinction likelihood, incorporating mechanisms that buffer organisms against partner loss. Specialized interactors, including 'cryptic specialists' with diverse but nonredundant partner assemblages, incur elevated risk. Risk is also higher for species that cannot either evolve new traits following partner loss or obtain novel partners in communities reorganizing under changing environmental conditions. Partner loss occurs alongside other anthropogenic impacts; multiple stressors can circumvent ecological buffers, enhancing secondary extinction risk. Stressors can also offset each other, reducing secondary extinction risk, a hitherto unappreciated phenomenon. This synthesis suggests improved conservation planning tactics and critical directions for research on secondary extinctions.

  7. Regional characteristics of the relationship between columnar AOD and surface PM2.5: Application of lidar aerosol extinction profiles over Baltimore-Washington Corridor during DISCOVER-AQ

    NASA Astrophysics Data System (ADS)

    Chu, D. Allen; Ferrare, Richard; Szykman, James; Lewis, Jasper; Scarino, Amy; Hains, Jennifer; Burton, Sharon; Chen, Gao; Tsai, Tzuchin; Hostetler, Chris; Hair, Johnathan; Holben, Brent; Crawford, James

    2015-01-01

    The first field campaign of DISCOVER-AQ (Deriving Information on Surface conditions from COlumn and VERtically resolved observations relevant to Air Quality) took place in July 2011 over Baltimore-Washington Corridor (BWC). A suite of airborne remote sensing and in-situ sensors was deployed along with ground networks for mapping vertical and horizontal distribution of aerosols. Previous researches were based on a single lidar station because of the lack of regional coverage. This study uses the unique airborne HSRL (High Spectral Resolution Lidar) data to baseline PM2.5 (particulate matter of aerodynamic diameter less than 2.5 μm) estimates and applies to regional air quality with satellite AOD (Aerosol Optical Depth) retrievals over BWC (∼6500 km2). The linear approximation takes into account aerosols aloft above AML (Aerosol Mixing Layer) by normalizing AOD with haze layer height (i.e., AOD/HLH). The estimated PM2.5 mass concentrations by HSRL AOD/HLH are shown within 2 RMSE (Root Mean Square Error ∼9.6 μg/m3) with correlation ∼0.88 with the observed over BWC. Similar statistics are shown when applying HLH data from a single location over the distance of 100 km. In other words, a single lidar is feasible to cover the range of 100 km with expected uncertainties. The employment of MPLNET-AERONET (MicroPulse Lidar NETwork - AErosol RObotic NETwork) measurements at NASA GSFC produces similar statistics of PM2.5 estimates as those derived by HSRL. The synergy of active and passive remote sensing aerosol measurements provides the foundation for satellite application of air quality on a daily basis. For the optimal range of 10 km, the MODIS-estimated PM2.5 values are found satisfactory at 27 (out of 36) sunphotometer locations with mean RMSE of 1.6-3.3 μg/m3 relative to PM2.5 estimated by sunphotometers. The remaining 6 of 8 marginal sites are found in the coastal zone, for which associated large RMSE values ∼4.5-7.8 μg/m3 are most likely due to

  8. Characterization of Chromophoric Water-Soluble Organic Matter in Urban, Forest, and Marine Aerosols by HR-ToF-AMS Analysis and Excitation-Emission Matrix Spectroscopy.

    PubMed

    Chen, Qingcai; Miyazaki, Yuzo; Kawamura, Kimitaka; Matsumoto, Kiyoshi; Coburn, Sean; Volkamer, Rainer; Iwamoto, Yoko; Kagami, Sara; Deng, Yange; Ogawa, Shuhei; Ramasamy, Sathiyamurthi; Kato, Shungo; Ida, Akira; Kajii, Yoshizumi; Mochida, Michihiro

    2016-10-04

    Chromophoric water-soluble organic matter in atmospheric aerosols potentially plays an important role in aqueous reactions and light absorption by organics. The fluorescence and chemical-structural characteristics of the chromophoric water-soluble organic matter in submicron aerosols collected in urban, forest, and marine environments (Nagoya, Kii Peninsula, and the tropical Eastern Pacific) were investigated using excitation-emission matrices (EEMs) and a high-resolution aerosol mass spectrometer. A total of three types of water-soluble chromophores, two with fluorescence characteristics similar to those of humiclike substances (HULIS-1 and HULIS-2) and one with fluorescence characteristics similar to those of protein compounds (PLOM), were identified in atmospheric aerosols by parallel factor analysis (PARAFAC) for EEMs. We found that the chromophore components of HULIS-1 and -2 were associated with highly and less-oxygenated structures, respectively, which may provide a clue to understanding the chemical formation or loss of organic chromophores in atmospheric aerosols. Whereas HULIS-1 was ubiquitous in water-soluble chromophores over different environments, HULIS-2 was abundant only in terrestrial aerosols, and PLOM was abundant in marine aerosols. These findings are useful for further studies regarding the classification and source identification of chromophores in atmospheric aerosols.

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

    SciTech Connect

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

    1993-03-20

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

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

    NASA Astrophysics Data System (ADS)

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

    1993-03-01

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

  11. Infrared spectroscopic methods for the study of aerosol particles using White cell optics: Development and characterization of a new aerosol flow tube.

    PubMed

    Nájera, Juan J; Fochesatto, Javier G; Last, Deborah J; Percival, Carl J; Horn, Andrew B

    2008-12-01

    A description of a new aerosol flow tube apparatus for measurements in situ under atmospherically relevant conditions is presented here. The system consists of a laboratory-made nebulizer generation system and a flow tube with a White cell-based Fourier transform IR for the detection system. An assessment of the White cell coupled to the flow tube was carried out by an extensive set of experiments to ensure the alignment of the infrared beam and optimize the performance of this system. The detection limit for CO was established as (1.0+/-0.3) ppm and 16 passes was chosen as the optimum number of passes to be used in flow tube experiments. Infrared spectroscopy was used to characterize dry aerosol particles in the flow tube. Pure particles composed of ammonium sulfate or sodium chloride ranging between 0.8 and 2.1 mum for size diameter and (0.8-4.9)x10(6) particles/cm(3) for density number were generated by nebulization of aqueous solutions. Direct measurements of the aerosol particle size agree with size spectra retrieved from inversion of the extinction measurements using Mie calculations, where the difference residual value is in the order of 0.2%. The infrared detection limit for ammonium sulfate aerosol particles was determined as d(p)=0.9 mum and N=5x10(3) particles/cm(3) with sigma=1.1 by Mie calculation. Alternatively, Mie calculations were performed to determine the flexibility in varying the optical length when aerosol particles are sent by the injector. The very good agreement between the values retrieved for aerosol particles injected through the flow tube or through the injector clearly validates the estimation of the effective optical path length for the injector. To determine the flexibility in varying the reaction zone length, analysis of the extinction spectra as function of the position of the injector was carried out by monitoring the integrated area of different absorption modes of the ammonium sulfate. We conclude that the aerosol loss in the

  12. Infrared spectroscopic methods for the study of aerosol particles using White cell optics: Development and characterization of a new aerosol flow tube

    NASA Astrophysics Data System (ADS)

    Nájera, Juan J.; Fochesatto, Javier G.; Last, Deborah J.; Percival, Carl J.; Horn, Andrew B.

    2008-12-01

    A description of a new aerosol flow tube apparatus for measurements in situ under atmospherically relevant conditions is presented here. The system consists of a laboratory-made nebulizer generation system and a flow tube with a White cell-based Fourier transform IR for the detection system. An assessment of the White cell coupled to the flow tube was carried out by an extensive set of experiments to ensure the alignment of the infrared beam and optimize the performance of this system. The detection limit for CO was established as (1.0±0.3) ppm and 16 passes was chosen as the optimum number of passes to be used in flow tube experiments. Infrared spectroscopy was used to characterize dry aerosol particles in the flow tube. Pure particles composed of ammonium sulfate or sodium chloride ranging between 0.8 and 2.1 μm for size diameter and (0.8-4.9)×106 particles/cm3 for density number were generated by nebulization of aqueous solutions. Direct measurements of the aerosol particle size agree with size spectra retrieved from inversion of the extinction measurements using Mie calculations, where the difference residual value is in the order of 0.2%. The infrared detection limit for ammonium sulfate aerosol particles was determined as dp=0.9 μm and N =5×103 particles/cm3 with σ =1.1 by Mie calculation. Alternatively, Mie calculations were performed to determine the flexibility in varying the optical length when aerosol particles are sent by the injector. The very good agreement between the values retrieved for aerosol particles injected through the flow tube or through the injector clearly validates the estimation of the effective optical path length for the injector. To determine the flexibility in varying the reaction zone length, analysis of the extinction spectra as function of the position of the injector was carried out by monitoring the integrated area of different absorption modes of the ammonium sulfate. We conclude that the aerosol loss in the flow tube

  13. Gradual extinction reduces reinstatement

    PubMed Central

    Shiban, Youssef; Wittmann, Jasmin; Weißinger, Mara; Mühlberger, Andreas

    2015-01-01

    The current study investigated whether gradually reducing the frequency of aversive stimuli during extinction can prevent the return of fear. Thirty-one participants of a three-stage procedure (acquisition, extinction and a reinstatement test on day 2) were randomly assigned to a standard extinction (SE) and gradual extinction (GE) procedure. The two groups differed only in the extinction procedure. While the SE group ran through a regular extinction process without any negative events, the frequency of the aversive stimuli during the extinction phase was gradually reduced for the GE group. The unconditioned stimulus (US) was an air blast (5 bar, 10 ms). A spider and a scorpion were used as conditioned stimuli (CS). The outcome variables were contingency ratings and physiological measures (skin conductance response, SCR and startle response). There were no differences found between the two groups for the acquisition and extinction phases concerning contingency ratings, SCR, or startle response. GE compared to SE significantly reduced the return of fear in the reinstatement test for the startle response but not for SCR or contingency ratings. This study was successful in translating the findings in rodent to humans. The results suggest that the GE process is suitable for increasing the efficacy of fear extinction. PMID:26441581

  14. Mass extinction: a commentary.

    PubMed

    Raup, D M

    1987-01-01

    Four neocatastrophist claims about mass extinction are currently being debated; they are that: 1, the late Cretaceous mass extinction was caused by large body impact; 2, as many as five other major extinctions were caused by impact; 3, the timing of extinction events since the Permian is uniformly periodic; and 4, the ages of impact craters on Earth are also periodic and in phase with the extinctions. Although strongly interconnected the four claims are independent in the sense that none depends on the others. Evidence for a link between impact and extinction is strong but still needs more confirmation through bed-by-bed and laboratory studies. An important area for future research is the question of whether extinction is a continuous process, with the rate increasing at times of mass extinctions, or whether it is episodic at all scales. If the latter is shown to be generally true, then species are at risk of extinction only rarely during their existence and catastrophism, in the sense of isolated events of extreme stress, is indicated. This is line of reasoning can only be considered an hypothesis for testing. In a larger context, paleontologists may benefit from a research strategy that looks to known Solar System and Galactic phenomena for predictions about environmental effects on earth. The recent success in the recognition of Milankovitch Cycles in the late Pleistocene record is an example of the potential of this research area.

  15. Mass extinction: a commentary

    NASA Technical Reports Server (NTRS)

    Raup, D. M.

    1987-01-01

    Four neocatastrophist claims about mass extinction are currently being debated; they are that: 1, the late Cretaceous mass extinction was caused by large body impact; 2, as many as five other major extinctions were caused by impact; 3, the timing of extinction events since the Permian is uniformly periodic; and 4, the ages of impact craters on Earth are also periodic and in phase with the extinctions. Although strongly interconnected the four claims are independent in the sense that none depends on the others. Evidence for a link between impact and extinction is strong but still needs more confirmation through bed-by-bed and laboratory studies. An important area for future research is the question of whether extinction is a continuous process, with the rate increasing at times of mass extinctions, or whether it is episodic at all scales. If the latter is shown to be generally true, then species are at risk of extinction only rarely during their existence and catastrophism, in the sense of isolated events of extreme stress, is indicated. This is line of reasoning can only be considered an hypothesis for testing. In a larger context, paleontologists may benefit from a research strategy that looks to known Solar System and Galactic phenomena for predictions about environmental effects on earth. The recent success in the recognition of Milankovitch Cycles in the late Pleistocene record is an example of the potential of this research area.

  16. Absorbing aerosols over Asia: A Geophysical Fluid Dynamics Laboratory general circulation model sensitivity study of model response to aerosol optical depth and aerosol absorption

    NASA Astrophysics Data System (ADS)

    Randles, C. A.; Ramaswamy, V.

    2008-11-01

    Forcing by absorbing atmospheric black carbon (BC) tends to heat the atmosphere, cool the surface, and reduce the surface latent and sensible heat fluxes. BC aerosol can have a large impact on regional climates and the hydrologic cycle. However, significant uncertainties remain concerning the increases in (1) the total amount of all aerosol species and (2) the amount of aerosol absorption that may have occurred over the 1950-1990 period. Focusing on south and east Asia, the sensitivity of a general circulation model's climate response (with prescribed sea surface temperatures and aerosol distributions) to such changes is investigated by considering a range of both aerosol absorption and aerosol extinction optical depth increases. We include direct and semidirect aerosol effects only. Precipitation changes are less sensitive to changes in aerosol absorption optical depth at lower aerosol loadings. At higher-extinction optical depths, low-level convergence and increases in vertical velocity overcome the stabilizing effects of absorbing aerosols and enhance the monsoonal circulation and precipitation in northwestern India. In contrast, the presence of increases in only scattering aerosols weakens the monsoonal circulation and inhibits precipitation here. Cloud amount changes can enhance or counteract surface solar flux reduction depending on the aerosol loading and absorption, with the changes also influencing the surface temperature and the surface energy balance. The results have implications for aerosol reduction strategies in the future that seek to mitigate air pollution concerns. At higher optical depths, if absorbing aerosol is present, reduction of scattering aerosol alone has a reduced effect on precipitation changes, implying that reductions in BC aerosols should be undertaken at the same time as reductions in sulfate aerosols.

  17. Measurements of Aerosol Vertical Profiles and Optical Properties during INDOEX 1999 Using Micro-Pulse Lidars

    NASA Technical Reports Server (NTRS)

    Welton, Ellsworth J.; Voss, Kenneth J.; Quinn, Patricia K.; Flatau, Piotr J.; Markowicz, Krzysztof; Campbell, James R.; Spinhirne, James D.; Gordon, Howard R.; Johnson, James E.; Starr, David OC. (Technical Monitor)

    2001-01-01

    Micro-pulse lidar systems (MPL) were used to measure aerosol properties during the Indian Ocean Experiment (INDOEX) 1999 field phase. Measurements were made from two platforms: the NOAA ship RN Ronald H. Brown, and the Kaashidhoo Climate Observatory (KCO) in the Maldives. Sunphotometers were used to provide aerosol optical depths (AOD) needed to calibrate the MPL. This study focuses on the height distribution and optical properties (at 523 nm) of aerosols observed during the campaign. The height of the highest aerosols (top height) was calculated and found to be below 4 km for most of the cruise. The marine boundary layer (MBL) top was calculated and found to be less than 1 km. MPL results were combined with air mass trajectories, radiosonde profiles of temperature and humidity, and aerosol concentration and optical measurements. Humidity varied from approximately 80% near the surface to 50% near the top height during the entire cruise. The average value and standard deviation of aerosol optical parameters were determined for characteristic air mass regimes. Marine aerosols in the absence of any continental influence were found to have an AOD of 0.05 +/- 0.03, an extinction-to-backscatter ratio (S-ratio) of 33 +/- 6 sr, and peak extinction values around 0.05/km (near the MBL top). The marine results are shown to be in agreement with previously measured and expected values. Polluted marine areas over the Indian Ocean, influenced by continental aerosols, had AOD values in excess of 0.2, S-ratios well above 40 sr, and peak extinction values approximately 0.20/km (near the MBL top). The polluted marine results are shown to be similar to previously published values for continental aerosols. Comparisons between MPL derived extinction near the ship (75 m) and extinction calculated at ship-level using scattering measured by a nephelometer and absorption using a PSAP were conducted. The comparisons indicated that the MPL algorithm (using a constant S-ratio throughout the

  18. 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

  19. SAGE II aerosol data validation and initial data use - An introduction and overview

    NASA Technical Reports Server (NTRS)

    Russell, P. B.; Mccormick, M. P.

    1989-01-01

    The process of validating data from the Stratospheric Aerosol and Gas Experiment (SAGE) II and the initial use of the validated data are reviewed. The instruments developed for the SAGE II, the influence of the eruption of El Chichon on the global stratospheric aerosol, and various data validation experiments are discussed. Consideration is given to methods for deriving aerosol physical and optical properties from SAGE II extinction data and for inferring particle size distribution moments from SAGE II spectral extinction values.

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

    SciTech Connect

    Richard A. Ferrare; David D. Turner

    2011-09-01

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

  1. Aerosol vertical distribution characteristics over the Tibetan Plateau

    NASA Astrophysics Data System (ADS)

    Deng, Z. Q.; Han, Y. X.; Zhao, Q.; Li, J.

    2014-03-01

    The Stratospheric Aerosol and Gas Experiment II (SAGE II) aerosol products are widely used in climatic characteristic studies and stratospheric aerosol pattern research. Some SAGE II products, e.g., temperature, aerosol surface area density, 1020 nm aerosol extinction coefficient and dust storm frequency, from ground-based observations were analysed from 1984 to 2005. This analysis explored the time and spatial variations of tropospheric and stratospheric aerosols on the Tibet Plateau. The stratospheric aerosol extinction coefficient increased more than two orders of magnitude because of a large volcanic eruption. However, the tropospheric aerosol extinction coefficient decreased over the same period. Removing the volcanic eruption effect, the correlation coefficient for stratospheric AOD (Aerosol Optical Depth) and tropospheric AOD was 0.197. Moreover, the correlation coefficient for stratospheric AOD and dust storm frequency was 0.315. The maximum stratospheric AOD was attained in January, the same month as the tropospheric AOD, when the Qaidam Basin was the centre of low tropospheric AOD and the large mountains coincided with high stratospheric AOD. The vertical structure generated by westerly jet adjustment and the high altitude of the underlying surface of the Tibetan Plateau were important factors affecting winter stratospheric aerosols.

  2. Aerosol effects and corrections in the Halogen Occultation Experiment

    NASA Technical Reports Server (NTRS)

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

    1995-01-01

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

  3. Organic aerosols

    SciTech Connect

    Penner, J.E.

    1994-01-01

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

  4. A diagnostic stratospheric aerosol size distribution inferred from SAGE II measurements

    NASA Technical Reports Server (NTRS)

    Thomason, Larry W.

    1991-01-01

    An aerosol size distribution model for the stratosphere is inferred based on 5 years of Stratospheric Aerosol and Gas Experiment (SAGE) II measurements of multispectral aerosol and water vapor extinction. The SAGE II aerosol and water vapor extinction data strongly suggest that there is a critical particle radius below which there is a relatively weak dependence of particle number density with size and above which there are few, if any, particles. A segmented power law model, as a simple representation of this dependence, is used in theoretical calculations and intercomparisons with a variety of aerosol measurements including dustsondes, longwave lidar, and wire impactors and shows a consistently good agreement.

  5. Vertical distributions of aerosol optical properties during haze and floating dust weather in Shanghai

    NASA Astrophysics Data System (ADS)

    Liu, Qiong; Wang, Yuan; Kuang, Zhongyu; Fang, Sihua; Chen, Yonghang; Kang, Yanming; Zhang, Hua; Wang, Daoyuan; Fu, Yingying

    2016-06-01

    A comparative study on the vertical distributions of aerosol optical properties during haze and floating dust weather in Shanghai was conducted based on the data obtained from a micro pulse lidar. There was a distinct difference in layer thickness and extinction coefficient under the two types of weather conditions. Aerosols were concentrated below 1 km and the aerosol extinction coefficients ranged from 0.25 to 1.50 km-1 on haze days. In contrast, aerosols with smaller extinction coefficients (0.20-0.35 km-1) accumulated mainly from the surface to 2 km on floating dust days. The seasonal variations of extinction and aerosol optical depth (AOD) for both haze and floating dust cases were similar—greatest in winter, smaller in spring, and smallest in autumn. More than 85% of the aerosols appeared in the atmosphere below 1 km during severe haze and floating dust weather. The diurnal variation of the extinction coefficient of haze exhibited a bimodal shape with two peaks in the morning or at noon, and at nightfall, respectively. The aerosol extinction coefficient gradually increased throughout the day during floating dust weather. Case studies showed that haze aerosols were generated from the surface and then lifted up, but floating dust aerosols were transported vertically from higher altitude to the surface. The AOD during floating dust weather was higher than that during haze. The boundary layer was more stable during haze than during floating dust weather.

  6. Airborne High Spectral Resolution Lidar Measurements of Atmospheric Aerosols

    NASA Astrophysics Data System (ADS)

    Ferrare, R.; Hostetler, C.; Hair, J.; Cook, A.; Harper, D.; Kleinman, L.; Clarke, A.; Russell, P.; Redemann, J.; Livingston, J.; Szykman, J.; Al-Saadi, J.

    2007-05-01

    NASA Langley Research Center (LaRC) recently developed an airborne High Spectral Resolution Lidar (HSRL) to measure aerosol distributions and optical properties. The HSRL technique takes advantage of the spectral distribution of the lidar return signal to discriminate aerosol and molecular signals and thereby measure aerosol extinction and backscatter independently. The LaRC instrument employs the HSRL technique to measure aerosol backscatter and extinction profiles at 532 nm and the standard backscatter lidar technique to measure aerosol backscatter profiles at 1064 nm. Depolarization profiles are measured at both wavelengths. Since March 2006, the airborne HSRL has acquired over 215 flight hours of data deployed on the NASA King Air B200 aircraft during several field experiments. Most of the flights were conducted during two major field experiments. The first major experiment was the joint Megacity Initiative: Local and Global Research Observations (MILAGRO) /Megacity Aerosol Experiment in Mexico City (MAX-MEX)/Intercontinental Chemical Transport Experiment-B (INTEX B) experiment that was conducted during March 2006 to investigate the evolution and transport of pollution from Mexico City. The second major experiment was the Texas Air Quality Study (TEXAQS)/Gulf of Mexico Atmospheric Composition and Climate Study (GoMACCS) that was conducted during August and September 2006 to investigate climate and air quality in the Houston/Gulf of Mexico region. Several flights were also conducted to help validate the Cloud-Aerosol LIdar with Orthogonal Polarization (CALIOP) lidar on board the Cloud-Aerosol Lidar and Infrared Pathfinder Satellite (CALIPSO) satellite. In February 2007, several flights were carried out as part of an Environmental Protection Agency (EPA) experiment to assess air quality in central California. Airborne HSRL data acquired during these missions were used to quantify aerosol extinction and optical thickness contributed by various aerosol types

  7. Flame extinction limit and particulates formation in fuel blends

    NASA Astrophysics Data System (ADS)

    Subramanya, Mahesh

    Many fuels used in material processing and power generation applications are generally a blend of various hydrocarbons. Although the combustion and aerosol formation dynamics of individual fuels is well understood, the flame dynamics of fuel blends are yet to be characterized. This research uses a twin flame counterflow burner to measure flame velocity, flame extinction, particulate formation and particulate morphology of hydrogen fuel blend flames at different H2 concentration, oscillation frequencies and stretch conditions. Phase resolved spectroscopic measurements (emission spectra) of OH, H, O and CH radical/atom concentrations is used to characterize the heat release processes of the flame. In addition flame generated particulates are collected using thermophoretic sample technique and are qualitative analyzed using Raman Spectroscopy and SEM. Such measurements are essential for the development of advanced computational tools capable of predicting fuel blend flame characteristics at realistic combustor conditions. The data generated through the measurements of this research are representative, and yet accurate, with unique well defined boundary conditions which can be reproduced in numerical computations for kinetic code validations.

  8. Beliefs about Human Extinction

    SciTech Connect

    Tonn, Bruce Edward

    2009-11-01

    This paper presents the results of a web-based survey about futures issues. Among many questions, respondents were asked whether they believe humans will become extinct. Forty-five percent of the almost 600 respondents believe that humans will become extinct. Many of those holding this believe felt that humans could become extinct within 500-1000 years. Others estimated extinction 5000 or more years into the future. A logistic regression model was estimated to explore the bases for this belief. It was found that people who describe themselves a secular are more likely to hold this belief than people who describe themselves as being Protestant. Older respondents and those who believe that humans have little control over their future also hold this belief. In addition, people who are more apt to think about the future and are better able to imagine potential futures tend to also believe that humans will become extinct.

  9. Stratospheric aerosol properties and their effects on infrared radiation.

    NASA Technical Reports Server (NTRS)

    Remsberg, E. E.

    1973-01-01

    This paper presents a stratospheric aerosol model and infers its effects on terrestrial radiation. Composition of the aerosol is assumed to be concentrated sulfuric acid. An appropriate size distribution has been determined from available size distribution measurements of other investigators. Aerosols composed of concentrated sulfuric acid emit energy in the atmospheric window region of the infrared spectrum, 8-13 microns. Laboratory measurements of optical constant data obtained at room temperature are presented for 75 and 90% aqueous sulfuric acid. Calculations of an aerosol extinction coefficient are then performed by using the above data. Effects of changes in aerosol phase and temperature are discussed but not resolved.

  10. SEAC4RS Aerosol Radiative Effects and Heating Rates

    NASA Astrophysics Data System (ADS)

    Cochrane, S.; Schmidt, S.; Redemann, J.; Hair, J. W.; Ferrare, R. A.; Segal-Rosenhaimer, M.; LeBlanc, S. E.

    2015-12-01

    We will present (a) aerosol optical properties, (b) aerosol radiative forcing, (c) aerosol and gas absorption and heating rates, and (d) spectral surface albedo for cases from August 19th and 26th of the SEAC4RS mission. This analysis is based on irradiance data from the Solar Spectral Flux Radiometer (SSFR), spectral aerosol optical depth from the Sky-Scanning, Sun-Tracking Atmospheric Research (4STAR), and extinction profiles from the DIAL/High Spectral Resolution Lidar (HSRL). We derive spectrally resolved values of single scattering albedo, asymmetry parameter, and surface albedo from the data, and determine profiles of absorption and heating rate segregated by absorber (aerosol and gas).

  11. Aerosol Classification using Airborne High Spectral Resolution Lidar Measurements

    NASA Astrophysics Data System (ADS)

    Burton, S. P.; Ferrare, R. A.; Hostetler, C. A.; Hair, J. W.; Obland, M. D.; Rogers, R.; Butler, C. F.; Cook, A.; Harper, D.; Froyd, K. D.

    2011-12-01

    The NASA Langley Research Center (LaRC) airborne High Spectral Resolution Lidar (HSRL) on the NASA B200 aircraft has acquired extensive datasets of aerosol extinction (532 nm), aerosol optical thickness (AOT) (532 nm), backscatter (532 and 1064 nm), and depolarization (532 and 1064 nm) profiles during 18 field missions that have been conducted over North America since 2006. The lidar measurements of aerosol intensive parameters (lidar ratio, depolarization, backscatter color ratio, spectral depolarization ratio) are shown to vary with location and aerosol type. A methodology based on observations of known aerosol types is used to qualitatively classify the extensive set of HSRL aerosol measurements into eight separate types. Several examples are presented showing how the aerosol intensive parameters vary with aerosol type and how these aerosols are classified according to this new methodology. The HSRL-based classification reveals vertical variability of aerosol types during the NASA ARCTAS field experiment conducted over Alaska and northwest Canada during 2008. In two examples derived from flights conducted during ARCTAS, the HSRL classification of biomass burning smoke is shown to be consistent with aerosol types derived from coincident airborne in situ measurements of particle size and composition. The HSRL retrievals of aerosol optical thickness and inferences of aerosol types are used to apportion aerosol optical thickness to aerosol type; results of this analysis are shown for several experiments.

  12. Extinction and the fossil record

    NASA Technical Reports Server (NTRS)

    Sepkoski, J. J. Jr; Sepkoski JJ, ,. J. r. (Principal Investigator)

    1994-01-01

    The author examines evidence of mass extinctions in the fossil record and searches for reasons for such large extinctions. Five major mass extinctions eliminated at least 40 percent of animal genera in the oceans and from 65 to 95 percent of ocean species. Questions include the occurrence of gradual or catastrophic extinctions, causes, environment, the capacity of a perturbation to cause extinctions each time it happens, and the possibility and identification of complex events leading to a mass extinction.

  13. Is extinction age dependent?

    USGS Publications Warehouse

    Doran, N.A.; Arnold, A.J.; Parker, W.C.; Huffer, F.W.

    2006-01-01

    Age-dependent extinction is an observation with important biological implications. Van Valen's Red Queen hypothesis triggered three decades of research testing its primary implication: that age is independent of extinction. In contrast to this, later studies with species-level data have indicated the possible presence of age dependence. Since the formulation of the Red Queen hypothesis, more powerful tests of survivorship models have been developed. This is the first report of the application of the Cox Proportional Hazards model to paleontological data. Planktonic foraminiferal morphospecies allow the taxonomic and precise stratigraphic resolution necessary for the Cox model. As a whole, planktonic foraminiferal morphospecies clearly show age-dependent extinction. In particular, the effect is attributable to the presence of shorter-ranged species (range < 4 myr) following extinction events. These shorter-ranged species also possess tests with unique morphological architecture. The morphological differences are probably epiphenomena of underlying developmental and heterochronic processes of shorter-ranged species that survived various extinction events. Extinction survivors carry developmental and morphological characteristics into postextinction recovery times, and this sets them apart from species populations established independently of extinction events. Copyright ?? 2006, SEPM (Society for Sedimentary Geology).

  14. SAGE II aerosol validation - Selected altitude measurements, including particle micromeasurements

    NASA Technical Reports Server (NTRS)

    Oberbeck, Verne R.; Russell, Philip B.; Pueschel, Rudolf F.; Snetsinger, Kenneth G.; Ferry, Guy V.; Livingston, John M.; Rosen, James N.; Osborn, Mary T.; Kritz, Mark A.

    1989-01-01

    The validity of particulate extinction coefficients derived from limb path solar radiance measurements obtained during the Stratospheric Aerosol and Gas Experiment (SAGE) II is tested. The SAGE II measurements are compared with correlative aerosol measurements taken during January 1985, August 1985, and July 1986 with impactors, laser spectrometers, and filter samplers on a U-2 aircraft, an upward pointing lidar on a P-3 aircraft, and balloon-borne optical particle counters. The data for July 29, 1986 are discussed in detail. The aerosol measurements taken on this day at an altitude of 20.5 km produce particulate extinction values which validate the SAGE II values for similar wavelengths.

  15. Relative Humidity Dependent Optical Properties of Clay Aerosols and their Mixtures

    NASA Astrophysics Data System (ADS)

    Greenslade, M. E.; Attwood, A. R.

    2012-12-01

    Mineral dust particles impact the Earth's radiative budget significantly because they comprise a large fraction of the total aerosol mass. Their impact is complex due to variable shapes and compositions that can cause optical properties to deviate from predictive models. A range of clay proxies for mineral dust including montmorillonite, illite and kaolinite have been interrogated with visible cavity ring down spectroscopy to determine the humidity dependent aerosol extinction. In addition, mixtures of montmorillonite with ammonium sulfate, sodium chloride, and three atmospherically relevant dicarboxylic acids (succinic, glutaric, and malonic acid) have been studied. The results are not always in agreement with simple models such as Mie theory or linear mixing rules based on the Zdanovskii, Stokes and Robinson method. Unexpected decreases in the fRH were observed for illite and kaolinite, but these can be explained based on physical and chemical composition. Similar to previous observations by other researchers, the deliquescence relative humidity was lower than predicted for mixed aerosols in cases where the salt fraction was large. The difference between experiment and model for all of the mixed aerosol species was greatest at higher relative humidity, especially above 80%. Explanations for these results will be discussed.

  16. A case study of dust aerosol radiative properties over Lanzhou, China

    NASA Astrophysics Data System (ADS)

    Zhang, L.; Cao, X.; Bao, J.; Zhou, B.; Huang, J.; Shi, J.; Bi, J.

    2010-05-01

    The vertical distribution of dust aerosol and its radiative properties are analysed using the data measured by the micropulse lidar, profiling microwave radiometer, sunphotometer, particulate monitor, and nephelometer at the Semi-Arid Climate and Environment Observatory of Lanzhou University (SACOL) during a dust storm from 27 March to 29 March 2007. The analysis shows that the dust aerosol mainly exists below 2 km in height, and the dust aerosol extinction coefficient decreases with height. The temporal evolution of aerosol optical depth (AOD) during the dust storm is characterized by a sub-maximum at 22:00 (Beijing Time), 27 March and a maximum at 12:00, 28 March. The AOD respectively derived by lidar and sunphotometer shows a good consistency. The PM10 concentration and aerosol scattering coefficient share similar variation trends, and their maximums both appear at 22:00, 27 March. The aerosol extinction coefficient and relative humidity have the similar trends and their maximums almost appear at the same heights, which presents a correlation between extinction coefficient and relative humidity known as aerosol hygroscopicity. The relative humidity is related with temperature, and then the temperature will affect the aerosol extinction properties by modifying the relative humidity condition. The aerosol extinction coefficient, scattering coefficient, and PM10 concentration present good linear correlations. The correlation coefficients of the aerosol scattering coefficients of 450, 520, and 700 nm and PM10 concentration, of aerosol extinction coefficient retrieved by lidar at 532 nm and PM10 concentration, and of aerosol extinction and scattering coefficient are respectively 0.98, 0.94, and 0.96.

  17. Protection from extinction.

    PubMed

    Rescorla, Robert A

    2003-05-01

    The effect of the presence of a conditioned inhibitor on extinction of excitatory conditioning was studied in one magazine approach and three autoshaping experiments using rats and pigeons. In each case, the presence of an inhibitor reduced responding to an exciter during extinction but allowed substantial recovery of responding to that exciter when subsequently tested separately. Control stimuli with a history of being irrelevant to reinforcement or being nonreinforced had less of a protective effect. This constitutes a clear demonstration of protection from extinction, a phenomenon of substantial theoretical and applied importance.

  18. Development of 2-D-MAX-DOAS and retrievals of trace gases and aerosols optical properties

    NASA Astrophysics Data System (ADS)

    Ortega, Ivan

    Air pollution is a major problem worldwide that adversely a_ects human health, impacts ecosystems and climate. In the atmosphere, there are hundreds of important compounds participating in complex atmospheric reactions linked to air quality and climate. Aerosols are relevant because they modify the radiation balance, a_ect clouds, and thus Earth albedo. The amount of aerosol is often characterized by the vertical integral through the entire height of the atmosphere of the logarithm fraction of incident light that is extinguished called Aerosol Optical Depth (AOD). The AOD at 550 nm (AOD550) over land is 0.19 (multi annual global mean), and that over oceans is 0.13. About 43 % of the Earth surface shows AOD550 smaller than 0.1. There is a need for measurement techniques that are optimized to measure aerosol optical properties under low AOD conditions, sample spatial scales that resemble satellite ground-pixels and atmospheric models, and help integrate remote sensing and in-situ observations to obtain optical closure on the effects of aerosols and trace gases in our changing environment. In this work, I present the recent development of the University of Colorado two dimensional (2-D) Multi-AXis Differential Optical Absorption Spectroscopy (2-D-MAX-DOAS) instrument to measure the azimuth and altitude distribution of trace gases and aerosol optical properties simultaneously with a single instrument. The instrument measures solar scattered light from any direction in the sky, including direct sun light in the hyperspectral domain. In Chapter 2, I describe the capabilities of 2-D measurements in the context of retrievals of azimuth distributions of nitrogen dioxide (NO2), formaldehyde (HCHO), and glyoxal (CHOCHO), which are precursors for tropospheric O3 and aerosols. The measurements were carried out during the Multi-Axis DOAS Comparison campaign for Aerosols and Trace gases (MAD-CAT) campaign in Mainz, Germany and show the ability to bridge spatial scales to

  19. Time-resolved studies of the interactions between pulsed lasers and aerosols.

    PubMed

    DeForest, Cindy L; Qian, Jun; Miller, Roger E

    2002-09-20

    Studies of the interaction between a pulsed CO2 laser and micrometer-sized aqueous and organic particles by use of light-scattering methods and step-scan Fourier-transform infrared (FTIR) spectroscopy are reported. Visible two-color extinction experiments indicate primary particle shattering, accompanied by a high fraction of vaporization, followed by secondary particle evaporation. The extent of the latter depends on the pulse intensity and particle composition. Angle-resolved light-scattering investigations provide insight into the aerosol size distribution and temperature following the pulsed heating event. The time dependence of the vapor plume, monitored with step-scan FTIR spectroscopy, confirms that a large fraction of the initial particle is quickly evaporated during the shattering event, followed by secondary fragment evaporation and thermal expansion.

  20. SAGE aerosol measurements. Volume 1: February 21, 1979 to December 31, 1979

    NASA Technical Reports Server (NTRS)

    Mccormick, M. P.

    1985-01-01

    The Stratospheric Aerosol and Gas Experiment (SAGE) satellite system, launched on February 18, 1979, provides profiles of aerosol extinction, ozone concentration, and nitrogen dioxide concentration between about 80 N and 80 S. Zonal averages, separated into sunrise and sunset events, and seasonal averages of the aerosol extinction at 1.00 microns and 0.45 microns ratios of the aerosol extinction to the molecular extinction at 1.00 microns, and ratios of the aerosol extinction at 0.45 microns to the aerosol extinction at 1.00 microns are given. The averages for 1979 are shown in tables and in profile and contour plots (as a function of altitude and latitude). In addition, temperature data provided by the National Oceanic and Atmospheric Administration (NOAA) for the time and location of each SAGE measurement are averaged and shown in a similar format. Typical values of the peak aerosol extinction were 0.0001 to 0.0002 km at 1.00 microns depth values for the 1.00 microns channel varied between 0.001 and 0.002 over all latitudes.

  1. Temporal Dynamics of Recovery from Extinction Shortly after Extinction Acquisition

    ERIC Educational Resources Information Center

    Archbold, Georgina E.; Dobbek, Nick; Nader, Karim

    2013-01-01

    Evidence suggests that extinction is new learning. Memory acquisition involves both short-term memory (STM) and long-term memory (LTM) components; however, few studies have examined early phases of extinction retention. Retention of auditory fear extinction was examined at various time points. Shortly (1-4 h) after extinction acquisition…

  2. Ground-based MAX-DOAS observations of tropospheric aerosols, NO2, SO2 and HCHO in Wuxi, China, from 2011 to 2014

    NASA Astrophysics Data System (ADS)

    Wang, Yang; Lampel, Johannes; Xie, Pinhua; Beirle, Steffen; Li, Ang; Wu, Dexia; Wagner, Thomas

    2017-02-01

    We characterize the temporal variation and vertical distribution of nitrogen dioxide (NO2), sulfur dioxide (SO2), formaldehyde (HCHO) and aerosol extinction based on long-term multi-axis differential optical absorption spectroscopy (MAX-DOAS) observations from May 2011 to November 2014 in Wuxi, China. A new inversion algorithm (PriAM) is implemented to retrieve profiles of the trace gases (TGs) and aerosol extinction (AE) from the UV spectra of scattered sunlight recorded by the MAX-DOAS instrument. We investigated two important aspects of the retrieval process. We found that the systematic seasonal variation of temperature and pressure (which is regularly observed in Wuxi) can lead to a systematic bias of the retrieved aerosol profiles (e.g. up to 20 % for the AOD) if it is not explicitly considered. In this study we take this effect into account for the first time. We also investigated in detail the reason for the differences of tropospheric vertical column densities derived from either the geometric approximation or by the integration of the retrieved profiles, which were reported by earlier studies. We found that these differences are almost entirely caused by the limitations of the geometric approximation (especially for high aerosol loads). The results retrieved from the MAX-DOAS observations are compared with independent techniques not only under cloud-free sky conditions, but also under various cloud scenarios. Under most cloudy conditions (except fog and optically thick clouds), the trace gas results still show good agreements. In contrast, for the aerosol results, only near-surface AE could be still well retrieved under cloudy situations. After applying a quality control procedure, the MAX-DOAS data are used to characterize the seasonal, diurnal and weekly variations of NO2, SO2, HCHO and aerosols. A regular seasonality of the three trace gases is found, but not for aerosols. Similar annual variations of the profiles of the trace gases appear in different

  3. Vertical distribution of the different types of aerosols in the stratosphere: Detection of solid particles and analysis of their spatial variability

    NASA Astrophysics Data System (ADS)

    Renard, Jean-Baptiste; Brogniez, Colette; Berthet, GwenaëL.; Bourgeois, Quentin; Gaubicher, Bertrand; Chartier, Michel; Balois, Jean-Yves; Verwaerde, Christian; Auriol, FréDéRique; Francois, Philippe; Daugeron, Daniel; Engrand, CéCile

    2008-11-01

    Stratospheric aerosols play a significant role in stratospheric chemistry. In the past, it was assumed that only liquid droplets are present in the stratosphere. Nevertheless, a few lidar measurements have shown that sudden enhancement of aerosol content in the middle stratosphere could be due to meteoritic debris. Aircraft measurements have shown that solid particles can be found in the lower stratosphere; these particles are mainly soot, but also include some interplanetary material. In order to better document the various characteristics of aerosols in the unperturbed stratosphere (i.e., free of volcanic aerosols), we have performed observations using different balloon-borne instruments (Stratospheric and Tropospheric Aerosol Counter (STAC), Spectroscopie d'Absorption Lunaire pour l'Observation des Minoritaires Ozone et NOx (SALOMON), and Micro Radiomètre Ballon (MicroRADIBAL)) and also some satellite data (Global ozone monitoring by occultation of stars Envisat (GOMOS-Envisat)). These instruments allow us to obtain the number of particles in different size classes, the wavelength dependence of aerosol extinction, and the radiance of the light scattered by aerosols. Combining all the data together, it appears that significant amounts of particles are ubiquitous in the middle stratosphere, above the canonical sulfate aerosol layer. "Background" interplanetary dusts in low concentration are likely present in the stratosphere. Above 30 km, interplanetary dust and largest grains from meteoroid disintegration dominate. Although the disintegration of meteoroids occurs in the upper stratosphere or in the mesosphere at all latitudes, these solid aerosols can be transported to the polar regions by the general circulation and can descend into the middle and lower stratosphere during winter mesospheric descents. Between about 22 km and 30 km, soot particles contribute to the population of aerosols at all latitudes. These soot, likely originating from biomass burning at

  4. Merging the SAGE II and OSIRIS Stratospheric Aerosol Records

    NASA Astrophysics Data System (ADS)

    Rieger, Landon; Bourassa, Adam; Degenstein, Doug

    2016-04-01

    The Optical Spectrograph and InfraRed Imaging System (OSIRIS) instrument on the Odin satellite, launched in 2001 and currently operational, measures limb-scattered sunlight from which profiles of stratospheric aerosol extinction at 750nm are retrieved. The Stratospheric Aerosol and Gas (SAGE) II instrument was operational from 1985 to 2005, and provided aerosol extinction at several visible and near infrared wavelengths. This work compares the SAGE II and OSIRIS aerosol extinction measurements during the four years of instrument overlap by interpolating the SAGE II data to 750nm using the 525 and 1020nm channels. Agreement is generally favourable in the tropics and mid-latitudes with differences less than 10% for the majority of the aerosol layer. However, near the UTLS and outside of the tropics agreement is poorer and reasons for this are investigated. Comparisons between the OSIRIS and SAGE II aerosol extinction measurements at 750nm are used to develop a merged aerosol climatology as a function of time, latitude and altitude at the native SAGE II wavelength of 525nm. Error due to assumptions in the OSIRIS retrieval and wavelength conversion are explored through simulation studies over a range of particle size distributions and is found to be approximately 20% for the majority of low-to-moderate volcanic loading conditions and OSIRIS geometries. Other sources of error such as cloud contamination in the UTLS are also explored.

  5. Measuring Optical Properties of SOOT from Biomass Burning Using Cavity RING-DOWN Spectroscopy and Integrating Nephelometry

    NASA Astrophysics Data System (ADS)

    Bililign, S.; Smith, D. M.; Fiddler, M. N.; Singh, S.; Colon-Bernal, I. D.

    2014-12-01

    Since black carbon and brown carbon are among the greatest contributors to radiative forcing (black carbon being second only to carbon dioxide), this work focuses on the laboratory measurement of their optical properties using cavity ring-down spectroscopy (CRDS) and integrating nephelometry. Water soluble soot is collected using an impinger by burning different fuel types to mimic ambient aerosols dominant in regions where biomass burning is the main source of aerosols. Using an optical parametric oscillator (OPO) as a light source, we are able to measure extinction and scattering over a wide range of wavelengths. The extinction-minus-scattering method is then used to determine particle absorption and single scattering albedo for soot collected from different fuel sources at different stages of burning. Purely scattering polystyrene latex (PSL) spheres of known sizes (100 - 700 nm) are used in the lab to calibrate the system for this study. Our preliminary measurements of optical properties of soot samples collected by burning different wood samples will be reported. A correction method that properly accounts for and reduces systematic extinction uncertainties, random scattering and extinction errors, and reconciles nephelometer with CRDS measurements is used.

  6. Properties of aerosol processed by ice clouds

    NASA Astrophysics Data System (ADS)

    Rudich, Y.; Adler, G.; Moise, T.; Erlick-Haspel, C.

    2012-12-01

    We suggest that highly porous aerosol (HPA) can form in the upper troposphere/lower stratosphere when ice particles encounter sub-saturation leading to ice sublimation similar to freeze drying. This process can occur at the lower layers of cirrus clouds (few km), at anvils of high convective clouds and thunderstorms, in clouds forming in atmospheric gravitational waves, in contrails and in high convective clouds injecting to the stratosphere. A new experimental system that simulates freeze drying of proxies for atmospheric aerosol at atmospheric pressure was constructed and various proxies for atmospheric soluble aerosol were studied. The properties of resulting HPA were characterized by various methods. It was found that the resulting aerosol have larger sizes (extent depends on substance and mixing), lower density (largevoid fraction), lower optical extinction and higher CCN activity and IN activity. Implication of HPA's unique properties and their atmospheric consequences to aerosol processing in ice clouds and to cloud cycles will be discussed.

  7. Extinction of oscillating populations

    NASA Astrophysics Data System (ADS)

    Smith, Naftali R.; Meerson, Baruch

    2016-03-01

    Established populations often exhibit oscillations in their sizes that, in the deterministic theory, correspond to a limit cycle in the space of population sizes. If a population is isolated, the intrinsic stochasticity of elemental processes can ultimately bring it to extinction. Here we study extinction of oscillating populations in a stochastic version of the Rosenzweig-MacArthur predator-prey model. To this end we develop a WKB (Wentzel, Kramers and Brillouin) approximation to the master equation, employing the characteristic population size as the large parameter. Similar WKB theories have been developed previously in the context of population extinction from an attracting multipopulation fixed point. We evaluate the extinction rates and find the most probable paths to extinction from the limit cycle by applying Floquet theory to the dynamics of an effective four-dimensional WKB Hamiltonian. We show that the entropic barriers to extinction change in a nonanalytic way as the system passes through the Hopf bifurcation. We also study the subleading pre-exponential factors of the WKB approximation.

  8. Extinction with multiple excitors.

    PubMed

    McConnell, Bridget L; Miguez, Gonzalo; Miller, Ralph R

    2013-06-01

    Four conditioned suppression experiments with rats, using an ABC renewal design, investigated the effects of compounding the target conditioned excitor with additional, nontarget conditioned excitors during extinction. Experiment 1 showed stronger extinction, as evidenced by less renewal, when the target excitor was extinguished in compound with a second excitor, relative to when it was extinguished with associatively neutral stimuli. Critically, this deepened extinction effect was attenuated (i.e., more renewal occurred) when a third excitor was added during extinction training. This novel demonstration contradicts the predictions of associative learning models based on total error reduction, but it is explicable in terms of a counteraction effect within the framework of the extended comparator hypothesis. The attenuated deepened extinction effect was replicated in Experiments 2a and 3, which also showed that pretraining consisting of weakening the association between the two additional excitors (Experiments 2a and 2b) or weakening the association between one of the additional excitors and the unconditioned stimulus (Experiment 3) attenuated the counteraction effect, thereby resulting in a decrease in responding to the target excitor. These results suggest that more than simple total error reduction determines responding after extinction.

  9. Aerosol Climate Time Series Evaluation In ESA Aerosol_cci

    NASA Astrophysics Data System (ADS)

    Popp, T.; de Leeuw, G.; Pinnock, S.

    2015-12-01

    Within the ESA Climate Change Initiative (CCI) Aerosol_cci (2010 - 2017) conducts intensive work to improve algorithms for the retrieval of aerosol information from European sensors. By the end of 2015 full mission time series of 2 GCOS-required aerosol parameters are completely validated and released: Aerosol Optical Depth (AOD) from dual view ATSR-2 / AATSR radiometers (3 algorithms, 1995 - 2012), and stratospheric extinction profiles from star occultation GOMOS spectrometer (2002 - 2012). Additionally, a 35-year multi-sensor time series of the qualitative Absorbing Aerosol Index (AAI) together with sensitivity information and an AAI model simulator is available. Complementary aerosol properties requested by GCOS are in a "round robin" phase, where various algorithms are inter-compared: fine mode AOD, mineral dust AOD (from the thermal IASI spectrometer), absorption information and aerosol layer height. As a quasi-reference for validation in few selected regions with sparse ground-based observations the multi-pixel GRASP algorithm for the POLDER instrument is used. Validation of first dataset versions (vs. AERONET, MAN) and inter-comparison to other satellite datasets (MODIS, MISR, SeaWIFS) proved the high quality of the available datasets comparable to other satellite retrievals and revealed needs for algorithm improvement (for example for higher AOD values) which were taken into account for a reprocessing. The datasets contain pixel level uncertainty estimates which are also validated. The paper will summarize and discuss the results of major reprocessing and validation conducted in 2015. The focus will be on the ATSR, GOMOS and IASI datasets. Pixel level uncertainties validation will be summarized and discussed including unknown components and their potential usefulness and limitations. Opportunities for time series extension with successor instruments of the Sentinel family will be described and the complementarity of the different satellite aerosol products

  10. Changes in the optical properties of benzo[a]pyrene-coated aerosols upon heterogeneous reactions with NO2 and NO3.

    PubMed

    Lu, Jessica W; Flores, J Michel; Lavi, Avi; Abo-Riziq, Ali; Rudich, Yinon

    2011-04-14

    Chemical reactions can alter the chemical, physical, and optical properties of aerosols. It has been postulated that nitration of aerosols can account for atmospheric absorbance over urban areas. To study this potentially important process, the change in optical properties of laboratory-generated benzo[a]pyrene (BaP)-coated aerosols following exposure to NO(2) and NO(3) was investigated at 355 nm and 532 nm by three aerosol analysis techniques. The extinction coefficient was determined at 355 nm and 532 nm from cavity ring-down aerosol spectroscopy (CRD-AS); the absorption coefficient was measured by photoacoustic spectroscopy (PAS) at 532 nm, while an on-line aerosol mass spectrometer (AMS) supplied real-time quantitative information about the chemical composition of aerosols. In this study, 240 nm polystyrene latex (PSL) spheres were thinly coated with BaP to form 300 or 310 nm aerosols that were exposed to high concentrations of NO(2) and NO(3) and measured with CRD-AS, PAS, and the AMS. The extinction efficiencies (Q(ext)) changed after exposure to NO(2) and NO(3) at both wavelengths. Prior to reaction, Q(ext) for the 355 nm and 532 nm wavelengths were 4.36 ± 0.04 and 2.39 ± 0.05, respectively, and Q(ext) increased to 5.26 ± 0.04 and 2.79 ± 0.05 after exposure. The absorption cross-section at 532 nm, determined with PAS, reached σ(abs) = (0.039 ± 0.001) × 10(-8) cm(2), indicating that absorption increased with formation of nitro-BaP, the main reaction product detected by the AMS. The single-scattering albedo (SSA), a measure of particle scattering efficiency, decreased from 1 to 0.85 ± 0.03, showing that changes in the optical properties of BaP-covered aerosols due to nitration may have implications for regional radiation budget and, hence, climate.

  11. Extinction and backscatter measurements of Antarctic PSC's, 1987: Implications for particle and vapor removal

    NASA Technical Reports Server (NTRS)

    Poole, L. R.; Mccormick, M. Patrick; Browell, Edward V.; Trepte, C. R.; Fahey, D. W.; Kelly, K. K.; Ferry, G. V.; Pueschel, R. F.; Jones, R. L.

    1988-01-01

    The temperature dependence is examined of optical properties measured in the Antarctic during 1987 at the 70 mb level (near 18 km), a level chosen to correlate the results with in situ measurements made from the NASA-Ames ER-2 aircraft during the 1987 Airborne Antarctic Ozone Experiment (AAOE). The data set consists of extinction measurements by Sam 2 inside the Antarctic polar vortex from May to October 1987; and backscatter measurements by the UV-DIAL (Ultraviolet Differential Absorption Lidar) system aboard the Ames DC-8 aircraft during selected AAOE flights. Observed trends are compared with results from a revised version of Pole and McCormick's model to classify the PSC observations by Type (1 or 2) and infer the temporal behavior of the ambient aerosol and ambient vapor mixing ratios. The sample figures show monthly ensembles of the 70-mb Sam 2 extinction ratio (the ratio of aerosol or PSC extinction to molecule extinction) as a function of NMC temperature at the beginning (June) and (October) of the 1987 Antarctic winter. Both ensembles show two rather distinct clusters of points: one oriented in the near vertical direction which depicts the change with temperature of the ambient aerosol extinction ratio; and a second cluster oriented in the near horizontal direction whose position on the vertical scale marks a change in particle phase (i.e., PSC formation) and whose length (the extinction enhancement related to that of the ambient aerosol) is an indicator of PSC type.

  12. Improving Aerosol and Visibility Forecasting Capabilities Using Current and Future Generations of Satellite Observations

    DTIC Science & Technology

    2015-08-27

    of the study period, a 3-D CALIOP DA scheme, which is coupled with 2D aerosol optical depth ( AOD ) assimilation using MODIS and MISR aerosol data, has...with the support of this project) has been developed by using the variance in radiances within an artificial light source to retrieve AOD (McHardy et... AOD ) data and lidar vertical aerosol extinction profiles from Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observations (CALIOP) has been

  13. Extinction of CO2 Laser Radiation Under Adverse Weather Conditions

    DTIC Science & Technology

    1982-06-01

    81-1280 B0 91,a 4 TITLE (and Subtitle) S TYPE OF REPORT & PERIOD COVERED EXTINCTION OF CO2 LASER RADIATION UNDER FINAL Oct 78 Oct 81 ADVERSE WEATHER...CONDITIONS 6 PERFORMING O0G r_ r NUMBER 7. AUTHOR( s ) 8 CONTRACT OR GRANT NUMBER( s ) Dr. Vincent Chimelis ŝ PERFORMING ORGANIZATION NAME AND ADDRESS 10...number) Laser Propagation Rain Laser Extinction CO2 Lasers Adverse Weather Aerosol s - 20 RACT (Continue on reverse side If necessary and Identify by

  14. Optical and Hygroscopic Studies of Aerosols In Simulated Planetary Atmospheres

    NASA Astrophysics Data System (ADS)

    Hasenkopf, Christa A.

    2011-08-01

    Basic characteristics of the early Earth climate, the only known environment in the Universe in which life has been known to emerge and thrive, remain a mystery. In particular, little is understood about the Earth's atmosphere 2.8 billion years ago. From climate models and laboratory studies, it is postulated that an organic haze, much like that found on Saturn's largest moon Titan, covered the early Earth. This haze, generated from photolysis of carbon dioxide (CO2) and methane (CH4), may have had profound climatic consequences. Climate models of the early Earth that include this haze have had to rely upon optical properties of a Titan laboratory analog. Titan haze, though thought to be similar, is formed from a different combination of precursor gases and by different energy sources than early Earth haze. This thesis examines the direct and indirect radiative effects of aerosol on early Earth climate by studying the optical and hygroscopic properties of a laboratory analog. A Titan analog is studied for comparison and to better understand spacecraft-retrieved haze chemical and optical properties from Titan. The properties of the laboratory analogs, generated in a flowing reactor cell with a continuum ultraviolet (UV) light source, were primarily measured using cavity ringdown aerosol extinction spectroscopy and UV-visible (UV-Vis) transmission spectroscopy. We find that the optical properties of our early Earth analog are significantly different than those of the Titan analog from Khare et al. (1984). In both the UV and visible, when modeled as fractals, particles with the optical properties of the early Earth analog have approximately 30% larger extinction efficiencies than particles with Khare et al. (1984) values. This result implies our early Earth haze analog would provide a more efficient UV shield and have a stronger antigreenhouse effect than the Khare et al. (1984) Titan analog. Our Titan analog has significantly smaller imaginary refractive index values

  15. Elevated aerosol layers modify the O2–O2 absorption measured by ground-based MAX-DOAS

    SciTech Connect

    Ortega, Ivan; Berg, Larry K.; Ferrare, Richard A.; Hair, Johnathan W.; Hostetler, Chris A.; Volkamer, Rainer

    2016-06-01

    The oxygen collisional complex (O2-O2, or O4) is a greenhouse gas, and a calibration trace gas used to infer aerosol and cloud properties by Differential Optical Absorption Spectroscopy (DOAS). Recent reports suggest the need for an O4 correction factor (CFO4) when comparing simulated and measured O4 differential slant column densities (dSCD) by passive DOAS. We investigate the sensitivity of O4 dSCD simulations at ultraviolet (360 nm) and visible (477 nm) wavelengths towards separately measured aerosol extinction profiles. Measurements were conducted by the University of Colorado 2D-MAX-DOAS instrument and NASA’s multispectral High Spectral Resolution Lidar (HSRL-2) during the Two Column Aerosol Project (TCAP) at Cape Cod, MA in July 2012. During two case study days with (1) high aerosol load (17 July, AOD ~ 0.35 at 477 nm), and (2) near molecular scattering conditions (22 July, AOD < 0.10 at 477 nm) the measured and calculated O4 dSCDs agreed within 6.4±0.4% (360 nm) and 4.7±0.6% (477 nm) if the HSRL-2 profiles were used as input to the calculations. However, if in the calculations the aerosol is confined to the surface layer (while keeping AOD constant) we find 0.53aerosol layers, unless accounted for, can cause negative bias in the simulated O4 dSCDs that can explain CFO4. The air density and aerosol profile aloft needs to be taken into account when interpreting the O4 from ground-based MAX-DOAS. Opportunities to identify and better characterize these layers are also discussed.

  16. Airborne Lidar Measurements of Aerosol Optical Properties During SAFARI-2000

    NASA Technical Reports Server (NTRS)

    McGill, M. J.; Hlavka, D. L.; Hart, W. D.; Welton, E. J.; Campbell, J. R.; Starr, David OC. (Technical Monitor)

    2002-01-01

    The Cloud Physics Lidar (CPL) operated onboard the NASA ER-2 high altitude aircraft during the SAFARI-2000 field campaign. The CPL provided high spatial resolution measurements of aerosol optical properties at both 1064 nm and 532 nm. We present here results of planetary boundary layer (PBL) aerosol optical depth analysis and profiles of aerosol extinction. Variation of optical depth and extinction are examined as a function of regional location. The wide-scale aerosol mapping obtained by the CPL is a unique data set that will aid in future studies of aerosol transport. Comparisons between the airborne CPL and ground-based MicroPulse Lidar Network (MPL-Net) sites are shown to have good agreement.

  17. 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.

  18. Stress and Fear Extinction

    PubMed Central

    Maren, Stephen; Holmes, Andrew

    2016-01-01

    Stress has a critical role in the development and expression of many psychiatric disorders, and is a defining feature of posttraumatic stress disorder (PTSD). Stress also limits the efficacy of behavioral therapies aimed at limiting pathological fear, such as exposure therapy. Here we examine emerging evidence that stress impairs recovery from trauma by impairing fear extinction, a form of learning thought to underlie the suppression of trauma-related fear memories. We describe the major structural and functional abnormalities in brain regions that are particularly vulnerable to stress, including the amygdala, prefrontal cortex, and hippocampus, which may underlie stress-induced impairments in extinction. We also discuss some of the stress-induced neurochemical and molecular alterations in these brain regions that are associated with extinction deficits, and the potential for targeting these changes to prevent or reverse impaired extinction. A better understanding of the neurobiological basis of stress effects on extinction promises to yield novel approaches to improving therapeutic outcomes for PTSD and other anxiety and trauma-related disorders. PMID:26105142

  19. A global aerosol classification algorithm incorporating multiple satellite data sets of aerosol and trace gas abundances

    NASA Astrophysics Data System (ADS)

    Penning de Vries, M. J. M.; Beirle, S.; Hörmann, C.; Kaiser, J. W.; Stammes, P.; Tilstra, L. G.; Tuinder, O. N. E.; Wagner, T.

    2015-09-01

    Detecting the optical properties of aerosols using passive satellite-borne measurements alone is a difficult task due to the broadband effect of aerosols on the measured spectra and the influences of surface and cloud reflection. We present another approach to determine aerosol type, namely by studying the relationship of aerosol optical depth (AOD) with trace gas abundance, aerosol absorption, and mean aerosol size. Our new Global Aerosol Classification Algorithm, GACA, examines relationships between aerosol properties (AOD and extinction Ångström exponent from the Moderate Resolution Imaging Spectroradiometer (MODIS), UV Aerosol Index from the second Global Ozone Monitoring Experiment, GOME-2) and trace gas column densities (NO2, HCHO, SO2 from GOME-2, and CO from MOPITT, the Measurements of Pollution in the Troposphere instrument) on a monthly mean basis. First, aerosol types are separated based on size (Ångström exponent) and absorption (UV Aerosol Index), then the dominating sources are identified based on mean trace gas columns and their correlation with AOD. In this way, global maps of dominant aerosol type and main source type are constructed for each season and compared with maps of aerosol composition from the global MACC (Monitoring Atmospheric Composition and Climate) model. Although GACA cannot correctly characterize transported or mixed aerosols, GACA and MACC show good agreement regarding the global seasonal cycle, particularly for urban/industrial aerosols. The seasonal cycles of both aerosol type and source are also studied in more detail for selected 5° × 5° regions. Again, good agreement between GACA and MACC is found for all regions, but some systematic differences become apparent: the variability of aerosol composition (yearly and/or seasonal) is often not well captured by MACC, the amount of mineral dust outside of the dust belt appears to be overestimated, and the abundance of secondary organic aerosols is underestimated in comparison

  20. Detection and quantification of water-based aerosols using active open-path FTIR

    NASA Astrophysics Data System (ADS)

    Kira, Oz; Linker, Raphael; Dubowski, Yael

    2016-04-01

    Aerosols have a leading role in many eco-systems and knowledge of their properties is critical for many applications. This study suggests using active Open-Path Fourier Transform Infra-Red (OP-FTIR) spectroscopy for quantifying water droplets and solutes load in the atmosphere. The OP-FTIR was used to measure water droplets, with and without solutes, in a 20 m spray tunnel. Three sets of spraying experiments generated different hydrosols clouds: (1) tap water only, (2) aqueous ammonium sulfate (0.25–3.6%wt) and (3) aqueous ethylene glycol (0.47–2.38%wt). Experiment (1) yielded a linear relationship between the shift of the extinction spectrum baseline and the water load in the line-of-sight (LOS) (R2 = 0.984). Experiment (2) also yielded a linear relationship between the integrated extinction in the range of 880–1150 cm‑1 and the ammonium sulfate load in the LOS (R2 = 0.972). For the semi-volatile ethylene glycol (experiment 3), present in the gas and condense phases, quantification was much more complex and two spectral approaches were developed: (1) according to the linear relationship from the first experiment (determination error of 8%), and (2) inverse modeling (determination error of 57%). This work demonstrates the potential of the OP-FTIR for detecting clouds of water-based aerosols and for quantifying water droplets and solutes at relatively low concentrations.

  1. 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.

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

    NASA Astrophysics Data System (ADS)

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

    2016-12-01

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

  3. Biological extinction in earth history

    NASA Technical Reports Server (NTRS)

    Raup, D. M.

    1986-01-01

    Virtually all plant and animal species that have ever lived on the earth are extinct. For this reason alone, extinction must play an important role in the evolution of life. The five largest mass extinctions of the past 600 million years are of greatest interest, but there is also a spectrum of smaller events, many of which indicate biological systems in profound stress. Extinction may be episodic at all scales, with relatively long periods of stability alternating with short-lived extinction events. Most extinction episodes are biologically selective, and further analysis of the victims and survivors offers the greatest chance of deducing the proximal causes of extinction. A drop in sea level and climatic change are most frequently invoked to explain mass extinctions, but new theories of collisions with extraterrestrial bodies are gaining favor. Extinction may be constructive in a Darwinian sense or it may only perturb the system by eliminating those organisms that happen to be susceptible to geologically rare stresses.

  4. Species extinction mires ecosystem

    SciTech Connect

    Holzman, D.

    1990-03-26

    Extinction is normal in the evolution of life, but amphibians, insects, birds and mammals are vanishing at an alarming pace. While habitat destruction, overexploitation and pollution are among the main causes, some disappearances cannot be explained. The extinction problem among amphibians mirrors the general, worldwide phenomenon. A synergism of insults may be responsible. Chance events such as a dry year might occasionally clean out a pond. But a larger lake nearby would replenish it. Now acid pollution adds to the ponds' burden while stocking of amphibian-eating sport fish in the lake - which happens even in natural parks - would destroy the source of replenishment. Some fear that extinctions ultimately could destroy nature's fabric.

  5. Correlation of aerosol mass near the ground with aerosol optical depth during two seasons in Munich

    NASA Astrophysics Data System (ADS)

    Schäfer, Klaus; Harbusch, Andreas; Emeis, Stefan; Koepke, Peter; Wiegner, Matthias

    2008-06-01

    Relations of the aerosol optical depth (AOD) with aerosol mass concentration near the ground, particulate matter (PM), have been studied on the basis of measurements. The objective is with respect to possible remote sensing methods to get information on the spatial and temporal variation of aerosols which is important for human health effects. Worldwide the AOD of the atmospheric column is routinely monitored by sun-photometers and accessible from satellite measurements also. It is implied here that the AOD is caused mainly by attenuation processes within the mixing layer because this layer includes nearly all atmospheric aerosols. Thus the mixing layer height (MLH) is required together with the AOD, measured by ground-based sun-photometers (around 560 nm), to get information about aerosols near the ground. MLH is determined here from surface-based remote sensing. Investigations were performed during two measurement campaigns in and near Munich in May and November/December 2003 on the basis of daily mean values. Using AOD and MLH measurements the aerosol extinction coefficient of the mixing layer has been calculated. This quantity was correlated with the measured PM10, PM2.5 and PM1 mass concentrations near the ground by performing a linear regression and thus providing a mass extinction efficiency giving squares of the correlation coefficients (R2) between 0.48 (PM1 during summer campaign) and 0.90 (PM2.5 during winter campaign). These correlations suggest that the derived mass extinction efficiencies represent a statistically significant relation between the aerosol extinction coefficients and the surface-based PM mass concentrations mainly during winter conditions.

  6. Analysis of Characteristics of Dust Aerosols in Northwest China based on Satellite Remote-sensing Data

    NASA Astrophysics Data System (ADS)

    Zhang, L.; Liu, L.; Zhao, Y.; Gong, S.; Henze, D. K.

    2014-12-01

    Based on the CloudSat data, effects of dust aerosol on cloud parameters under the circumstance of the monthly average, dusty days and dust-free days were analyzed during April, 2010. By using L2 aerosol profiles satellite data of CALIOP/CALIOPSO the aerosol extinction coefficients were analyzed over northwest China. As an important case, space distribution and transmission route of dust aerosol were investigated during the dust events occurred from April 16th to 18th in 2013 over northwest China, based on L1 data of CALIOP/CALIOPSO, a combination of multiple satellite data and models. The results show that (1) dust aerosols could cause the reduction in effective radius of particle, cloud liquid water content and cloud optical thickness, and the increase of the number concentration of liquid cloud particles as well, (2) The aerosol extinction coefficients were decreased with the increase of height. The value of the aerosol extinction coefficients in desert area was greater than that in the area of Gansu Province due to urbanization. Distribution of the aerosol extinction coefficients in spring was nearly the same as the annual average. (3) Using aerosol products of the vertical characteristics from CALIOP/CALIOPSO, aerosol was classified during dust events, and with NAPPS Global aerosol model, daily distribution of the dust aerosol concentration was given, showing the transport and diffusion of dust aerosol. With HYSPLIT trajectory model dust transportation path of the sand dust source areas was simulated and identified. During the outbreak of dust event dust aerosol was mainly distributed over the surface about 3km, with depolarization ratio at 0.4 and color ratio at 1.2. During the dust events were close to weak and stop, dust aerosol was mainly distributed over the surface under 2 km, with depolarization ratio from 0.2 to 0.3, and color ratio about 1.

  7. Analysis of Characteristics of Dust Aerosols in Northwest China based on Satellite Remote-sensing Data

    NASA Astrophysics Data System (ADS)

    Zhang, W.; Liu, D.; Zhao, Q.

    2015-12-01

    Based on the CloudSat data, effects of dust aerosol on cloud parameters under the circumstance of the monthly average, dusty days and dust-free days were analyzed during April, 2010. By using L2 aerosol profiles satellite data of CALIOP/CALIOPSO the aerosol extinction coefficients were analyzed over northwest China. As an important case, space distribution and transmission route of dust aerosol were investigated during the dust events occurred from April 16th to 18th in 2013 over northwest China, based on L1 data of CALIOP/CALIOPSO, a combination of multiple satellite data and models. The results show that (1) dust aerosols could cause the reduction in effective radius of particle, cloud liquid water content and cloud optical thickness, and the increase of the number concentration of liquid cloud particles as well, (2) The aerosol extinction coefficients were decreased with the increase of height. The value of the aerosol extinction coefficients in desert area was greater than that in the area of Gansu Province due to urbanization. Distribution of the aerosol extinction coefficients in spring was nearly the same as the annual average. (3) Using aerosol products of the vertical characteristics from CALIOP/CALIOPSO, aerosol was classified during dust events, and with NAPPS Global aerosol model, daily distribution of the dust aerosol concentration was given, showing the transport and diffusion of dust aerosol. With HYSPLIT trajectory model dust transportation path of the sand dust source areas was simulated and identified. During the outbreak of dust event dust aerosol was mainly distributed over the surface about 3km, with depolarization ratio at 0.4 and color ratio at 1.2. During the dust events were close to weak and stop, dust aerosol was mainly distributed over the surface under 2 km, with depolarization ratio from 0.2 to 0.3, and color ratio about 1.

  8. Satellite-Derived Extinction at A Desert Site

    NASA Astrophysics Data System (ADS)

    Walker, P. L.; Blomshield, F. S.

    2002-12-01

    We have been conducting research aimed at enabling determination of desert optical environments from meteorological and satellite observations. To this end we have been making Rotating Shadowband Radiometer measurements, collecting aerosol size distributions, visibility and meteorological data continuously for the past 2 years in the Indian Wells Valley of the Mojave Desert of California. These data present an opportunity to validate satellite retrieval of atmospheric optical depth. Specifically, MISR-derived optical depths are compared to those derived from Shadowband measurements. A crude measure of extinction can be made by dividing the optical depth by the height of the mixing layer. The validity of this procedure is determined by comparison with extinction directly measured by nephelometers and calculated from measured aerosol size distributions.

  9. Supernovae and mass extinctions

    NASA Technical Reports Server (NTRS)

    Vandenbergh, S.

    1994-01-01

    Shklovsky and others have suggested that some of the major extinctions in the geological record might have been triggered by explosions of nearby supernovae. The frequency of such extinction events will depend on the galactic supernova frequency and on the distance up to which a supernova explosion will produce lethal effects upon terrestrial life. In the present note it will be assumed that a killer supernova has to occur so close to Earth that it will be embedded in a young, active, supernova remnant. Such young remnants typically have radii approximately less than 3 pc (1 x 10(exp 19) cm). Larger (more pessimistic?) killer radii have been adopted by Ruderman, Romig, and by Ellis and Schramm. From observations of historical supernovae, van den Bergh finds that core-collapse (types Ib and II) supernovae occur within 4 kpc of the Sun at a rate of 0.2 plus or minus 0.1 per century. Adopting a layer thickness of 0.3 kpc for the galacitc disk, this corresponds to a rate of approximately 1.3 x 10(exp -4) supernovae pc(exp -3) g.y.(exp -1). Including supernovae of type Ia will increase the total supernovae rate to approximately 1.5 x 10(exp -4) supernovae pc(exp -3) g.y.(exp -1). For a lethal radius of R pc the rate of killer events will therefore be 1.7 (R/3)(exp 3) x 10(exp -2) supernovae per g.y. However, a frequency of a few extinctions per g.y. is required to account for the extinctions observed during the phanerozoic. With R (extinction) approximately 3 pc, the galactic supernova frequency is therefore too low by 2 orders of magnitude to account for the major extinctions in the geological record.

  10. Extinction from a paleontological perspective

    NASA Technical Reports Server (NTRS)

    Raup, D. M.

    1993-01-01

    Extinction of widespread species is common in evolutionary time (millions of years) but rare in ecological time (hundreds or thousands of years). In the fossil record, there appears to be a smooth continuum between background and mass extinction; and the clustering of extinctions at mass extinctions cannot be explained by the chance coincidence of independent events. Although some extinction is selective, much is apparently random in that survivors have no recognizable superiority over victims. Extinction certainly plays an important role in evolution, but whether it is constructive or destructive has not yet been determined.

  11. A new description of Titan's aerosol optical properties from the analysis of VIMS Emission Phase Function observations

    NASA Astrophysics Data System (ADS)

    Rodriguez, Sebastien; Maltagliati, Luca; Sotin, Christophe; Rannou, Pascal; Bézard, Bruno; Cornet, Thomas

    2016-10-01

    The Huygens probe gave unprecedented information on the properties of Titan's aerosols (vertical distribution, opacity as a function of wavelength, phase function, single scattering albedo) by in-situ measurements (Tomasko et al. 2008). Being the only existing in-situ atmospheric probing for Titan, this aerosol model currently is the reference for many Titan studies (e.g. by being applied as physical input in radiative transfer models of the atmosphere). Recently a reanalysis of the DISR dataset, corroborated by data from the Downward-Looking Visible Spectrometer (DLVS), was carried out by the same group (Doose et al. 2016), leading to significant changes to the indications given by Tomasko et al. (2008).Here we present the analysis of the Emission Phase Function observation (EPF) performed by VIMS during the Cassini flyby T88 (November 2012). An EPF observes the same spot on the surface (and thus the same atmosphere) with the same emergence angle but with different incidence angles. In this way, our EPF allows, for the first time, to have direct information on the phase function of Titan's aerosols, as well as on other important physical parameters of the aerosols as the behavior of their extinction as a function of wavelength and the single scattering albedo (also as a function of wavelength) for the whole VIMS range (0.8-5.2 μm). The T88 EPF is composed of 25 VIMS datacubes spanning a scattering angle range approximately from 0°to 70°.We used the radiative transfer model described in Hirtzig et al. (2013) as baseline, updated with improved methane (+ related isotopes) spectroscopy. By changing the aerosol description in the model, we found the combination of aerosol optical parameters that fits best a constant aerosol column density over the whole set of the VIMS datacubes. We confirmed that the new results from Doose et al. (2016) do improve the fit for what concerns the vertical profile and the extinction as a function of wavelength. However, a different

  12. A new description of Titan's aerosol optical properties from the analysis of VIMS Emission Phase Function observations

    NASA Astrophysics Data System (ADS)

    Maltagliati, Luca; Rodriguez, Sebastien; Sotin, Christophe; Rannou, Pascal; Bezard, Bruno; Cornet, Thomas

    2016-06-01

    The Huygens probe gave unprecedented information on the properties of Titan's aerosols (vertical distribution, opacity as a function of wavelength, phase function, single scattering albedo) by in-situ measurements (Tomasko et al. 2008). Being the only existing in-situ atmospheric probing for Titan, this aerosol model currently is the reference for many Titan studies (e.g. by being applied as physical input in radiative transfer models of the atmosphere). Recently a reanalysis of the DISR dataset, corroborated by data from the Downward-Looking Visible Spectrometer (DLVS), was carried out by the same group (Doose et al. 2016), leading to significant changes to the indications given by Tomasko et al. (2008). Here we present the analysis of the Emission Phase Function observation (EPF) performed by VIMS during the Cassini flyby T88 (November 2012). An EPF observes the same spot on the surface (and thus the same atmosphere) with the same emergence angle but with different incidence angles. In this way, our EPF allows, for the first time, to have direct information on the phase function of Titan's aerosols, as well as on other important physical parameters of the aerosols as the behavior of their extinction as a function of wavelength and the single scattering albedo (also as a function of wavelength) for the whole VIMS range (0.8-5.2 µm). The T88 EPF is composed of 25 VIMS datacubes spanning a scattering angle range approximately from 0°to 70°. We used the radiative transfer model described in Hirtzig et al. (2013) as baseline, updated with improved methane (+ related isotopes) spectroscopy. By changing the aerosol description in the model, we found the combination of aerosol optical parameters that fits best a constant aerosol column density over the whole set of the VIMS datacubes. We confirmed that the new results from Doose et al. (2016) do improve the fit for what concerns the vertical profile and the extinction as a function of wavelength. However, a different

  13. Scattering and Absorption of E&M radiation by small particles-applications to study impact of biomass aerosols on climate

    NASA Astrophysics Data System (ADS)

    Bililign, Solomon; Singh, Sujeeta; Fiddler, Marc; Smith, Damon

    2015-03-01

    The phenomena of scattering, absorption, and emission of light and other electromagnetic radiation by small particles are central to many science and engineering disciplines. Absorption of solar radiation by black carbon aerosols has a significant impact on the atmospheric energy distribution and hydrologic processes. By intercepting incoming solar radiation before it reaches the surface, aerosols heat the atmosphere and, in turn, cool the surface. The magnitude of the atmospheric forcing induced by anthropogenic absorbing aerosols, mainly black carbon (BC) emitted from biomass burning and combustion processes has been suggested to be comparable to the atmospheric forcing by all greenhouse gases (GHGs). Despite the global abundance of biomass burning for cooking, forests clearing for agriculture and wild fires, the optical properties of these aerosols have not been characterized at wide range of wavelengths. Our laboratory uses a combination of Cavity ring down spectroscopy and integrating nephelometry to measure optical properties of (extinction, absorption and scattering coefficients) of biomass aerosols. Preliminary results will be presented. Supported by the Department of Defense under Grant #W911NF-11-1-0188.

  14. Contrasting organic aerosol particles from boreal and tropical forests during HUMPPA-COPEC-2010 and AMAZE-08 using coherent vibrational spectroscopy

    NASA Astrophysics Data System (ADS)

    Ebben, C. J.; Martinez, I. S.; Shrestha, M.; Buchbinder, A. M.; Corrigan, A. L.; Guenther, A.; Karl, T.; Petäjä, T.; Song, W. W.; Zorn, S. R.; Artaxo, P.; Kulmala, M.; Martin, S. T.; Russell, L. M.; Williams, J.; Geiger, F. M.

    2011-10-01

    We present the vibrational sum frequency generation spectra of organic particles collected in a boreal forest in Finland and a tropical forest in Brazil. These spectra are compared to those of secondary organic material produced in the Harvard Environmental Chamber. By comparing coherent vibrational spectra of a variety of terpene and olefin reference compounds, along with the secondary organic material synthesized in the environmental chamber, we show that submicron aerosol particles sampled in Southern Finland during HUMPPA-COPEC-2010 are composed to a large degree of material similar in chemical composition to synthetic α-pinene-derived material. For material collected in Brazil as part of AMAZE-08, the organic component is found to be chemically complex in the coarse mode but highly uniform in the fine mode. When combined with histogram analyses of the isoprene and monoterpene abundance recorded during the HUMPPA-COPEC-2010 and AMAZE-08 campaigns, the findings presented here indicate that if air is rich in monoterpenes, submicron-sized secondary aerosol particles that form under normal OH and O3 concentration levels can be described in terms of their hydrocarbon content as being similar to α-pinene-derived model secondary organic aerosol particles. If the isoprene concentration dominates the chemical composition of organic compounds in forest air, then the hydrocarbon component of secondary organic material in the submicron size range is not simply well-represented by that of isoprene-derived model secondary organic aerosol particles but is more complex. Throughout the climate-relevant size range of the fine mode, however, we find that the chemical composition of the secondary organic particle material from such air is invariant with size, suggesting that the particle growth does not change the chemical composition of the hydrocarbon component of the particles in a significant way.

  15. Contrasting organic aerosol particles from boreal and tropical forests during HUMPPA-COPEC-2010 and AMAZE-08 using coherent vibrational spectroscopy

    NASA Astrophysics Data System (ADS)

    Ebben, C. J.; Martinez, I. S.; Shrestha, M.; Buchbinder, A. M.; Corrigan, A. L.; Guenther, A.; Karl, T.; Petäjä, T.; Song, W. W.; Zorn, S. R.; Artaxo, P.; Kulmala, M.; Martin, S. T.; Russell, L. M.; Williams, J.; Geiger, F. M.

    2011-06-01

    We present the vibrational sum frequency generation spectra of organic particles collected in a boreal forest in Finland and a tropical forest in Brazil. These spectra are compared to those of secondary organic material produced in the Harvard Environmental Chamber. By comparing coherent vibrational spectra of a variety of terpene and olefin reference compounds, along with the secondary organic material synthesized in the environmental chamber, we show that submicron aerosol particles sampled in Southern Finland during HUMPPA-COPEC-2010 are composed to a large degree of material similar in chemical composition to synthetic α-pinene-derived material. For material collected in Brazil as part of AMAZE-08, the organic component is found to be chemically complex in the coarse mode but highly uniform in the fine mode. When combined with histogram analyses of the isoprene and monoterpene abundance recorded during the HUMPPA-COPEC-2010 and AMAZE-08 campaigns, the findings presented here indicate that if air is rich in monoterpenes, submicron-sized secondary aerosol particles that form under normal OH and O3 concentration levels can be described in terms of their hydrocarbon content as being similar to α-pinene-derived model secondary organic aerosol particles. If the isoprene concentration dominates the chemical composition of organic compounds in forest air, then the hydrocarbon component of secondary organic material in the submicron size range is not simply well-represented by that of isoprene-derived model secondary organic aerosol particles but is more complex. Throughout the climate-relevant size range of the fine mode, however, we find that the chemical composition of the secondary organic particle material from such air is invariant with size, suggesting that the particle growth does not change the chemical composition of the hydrocarbon component of the particles in a significant way.

  16. Protostars at Low Extinction in Orion A

    NASA Astrophysics Data System (ADS)

    Lewis, John Arban; Lada, Charles J.

    2016-07-01

    In the list of young stellar objects (YSOs) compiled by Megeath et al. for the Orion A molecular cloud, only 44 out of 1208 sources found projected onto low extinction ({A}{{K}}\\lt 0.8 mag) gas are identified as protostars. These objects are puzzling because protostars are not typically expected to be associated with extended low extinction material. Here, we use high resolution extinction maps generated from Herschel data, optical/infrared and Spitzer Space Telescope photometry and spectroscopy of the low extinction protostellar candidate sources to determine if they are likely true protostellar sources or contaminants. Out of 44 candidate objects, we determine that 10 sources are likely protostars, with the rest being more evolved YSOs (18), galaxies (4), false detections of nebulosity and cloud edges (9), or real sources for which more data are required to ascertain their nature (3). We find none of the confirmed protostars to be associated with recognizable dense cores and we briefly discuss possible origins for these orphaned objects.

  17. A model for the separation of cloud and aerosol in SAGE II occultation data

    NASA Technical Reports Server (NTRS)

    Kent, G. S.; Winker, D. M.; Osborn, M. T.; Skeens, K. M.

    1993-01-01

    The Stratospheric Aerosol and Gas Experiment (SAGE) II satellite experiment measures the extinction due to aerosols and thin cloud, at wavelengths of 0.525 and 1.02 micrometers, down to an altitude of 6 km. The wavelength dependence of the extinction due to aerosols differs from that of the extinction due to cloud and is used as the basis of a model for separating these two components. The model is presented and its validation using airborne lidar data, obtained coincident with SAGE II observations, is described. This comparison shows that smaller SAGE II cloud extinction values correspond to the presence of subvisible cirrus cloud in the lidar record. Examples of aerosol and cloud data products obtained using this model to interpret SAGE II upper tropospheric and lower stratospheric data are also shown.

  18. Biogeography and extinction

    SciTech Connect

    Jablonski, D.

    1985-01-01

    The geographic ranges of species and clades, and the deployment of those clades among biogeographic provinces, are important determinants of rates and patterns of extinction. Studies of Late Cretaceous mollusks of the Gulf and Atlantic Coastal Plain confirm that species duration is closely correlated with geographic range during times of normal, background extinction. When species that originate in the last 2 myr of the Cretaceous, the correlation increases significantly. The fact that even these truncated species frequently attained broad geographic ranges indicates that during background times duration is a function of geographic range and not vice versa. However, during the end-Cretaceous mass extinction, it is clade geographic range and not the within-province ranges of its constituent species that determines survivorship: about 55% of the widespread genera but only 12% of the endemic genera survive, regardless of the ranges of their individual species. Thus, clade geographic range is an irreducible property, with effects decoupled from species-level or organismic traits that determine species' geographic ranges. Clades with tropical distributions suffer disproportionately, again independent of species' geographic range magnitudes. Survivorship of taxa or morphologies during mass extinctions may have little to do with adaptation at the organismic or even species level, but depends at least in part on clade-level traits that are less important during background times.

  19. Context, Learning, and Extinction

    ERIC Educational Resources Information Center

    Gershman, Samuel J.; Blei, David M.; Niv, Yael

    2010-01-01

    A. Redish et al. (2007) proposed a reinforcement learning model of context-dependent learning and extinction in conditioning experiments, using the idea of "state classification" to categorize new observations into states. In the current article, the authors propose an interpretation of this idea in terms of normative statistical inference. They…

  20. The mechanisms causing extinction debts.

    PubMed

    Hylander, Kristoffer; Ehrlén, Johan

    2013-06-01

    Extinction debts can result from many types of habitat changes involving mechanisms other than metapopulation processes. This is a fact that most recent literature on extinction debts pays little attention to. We argue that extinction debts can arise because (i) individuals survive in resistant life-cycle stages long after habitat quality change, (ii) stochastic extinctions of populations that have become small are not immediate, and (iii) metapopulations survive long after that connectivity has decreased if colonization-extinction dynamics is slow. A failure to distinguish between these different mechanisms and to simultaneously consider both the size of the extinction debt and the relaxation time hampers our understanding of how extinction debts arise and our ability to prevent ultimate extinctions.

  1. Extinction of Light during the Fog Life Cycle: a Result from the ParisFog Experiment

    SciTech Connect

    Elias, T.; Haeffelin, M.; Drobinski, P.

    2009-03-11

    Data set acquired by five particle-dedicated instruments set up on the SIRTA experimental site during the ParisFog field campaign are exploited to document microphysical properties of particles contributing to extinction of visible radiation in variable situations. The case study is a 48-hour period when atmospheric conditions are highly variable: relative humidity changes between 50 and 100%, visibility ranges between 35000 and 65 m, the site is either downwind Paris area either under maritime influence. A dense and homogeneous fog formed by radiative cooling during the 18-19 February night. In 7 hours, visibility decreases from 26 000 m to 65 m, because of transported pollution (factor 3 in visibility reduction), aerosol hydration (factor 20) and aerosol activation (factor 6). According to Mie theory, extinction in clear-sky polluted and unpolluted regimes is due equally to Aitken and accumulation modes. Extinction in haze is due to hydrated aerosols distributed in the accumulation mode, for diameter smaller than 2 {mu}m. Hydrated aerosols of the accumulation mode still contribute to 20-30% extinction in the fog. Measurements show that fog droplets, with diameter included between 2 and 10 {mu}m, contribute to 40% extinction during the first hours of the fog.

  2. Composition and physical properties of the Asian Tropopause Aerosol Layer and the North American Tropospheric Aerosol Layer

    PubMed Central

    Yu, Pengfei; Toon, Owen B; Neely, Ryan R; Martinsson, Bengt G; Brenninkmeijer, Carl A M

    2015-01-01

    Recent studies revealed layers of enhanced aerosol scattering in the upper troposphere and lower stratosphere over Asia (Asian Tropopause Aerosol Layer (ATAL)) and North America (North American Tropospheric Aerosol Layer (NATAL)). We use a sectional aerosol model (Community Aerosol and Radiation Model for Atmospheres (CARMA)) coupled with the Community Earth System Model version 1 (CESM1) to explore the composition and optical properties of these aerosol layers. The observed aerosol extinction enhancement is reproduced by CESM1/CARMA. Both model and observations indicate a strong gradient of the sulfur-to-carbon ratio from Europe to the Asia on constant pressure surfaces. We found that the ATAL is mostly composed of sulfates, surface-emitted organics, and secondary organics; the NATAL is mostly composed of sulfates and secondary organics. The model also suggests that emission increases in Asia between 2000 and 2010 led to an increase of aerosol optical depth of the ATAL by 0.002 on average which is consistent with observations. Key Points The Asian Tropopause Aerosol Layer is composed of sulfate, primary organics, and secondary organics The North American Tropospheric Aerosol Layer is mostly composed of sulfate and secondary organics Aerosol Optical Depth of Asian Tropopause Aerosol Layer increases by 0.002 from 2000 to 2010 PMID:26709320

  3. Aerosol characterization and transport pathway using ground-based measurement and space borne remote sensing

    NASA Astrophysics Data System (ADS)

    Boyouk, Neda; Léon, Jean-François; Delbarre, Hervé

    2008-10-01

    Using two years measurements of aerosol extinction coefficient retrieval from CALIPSO as a joint NASA-CNES satellite mission along with ground-based measurements of particle mass concentration (PM2.5), we assess particulate matter air quality over different urban and periurban areas in France. In order to understanding the influence of the long range transport onto the local aerosol load we have focused on analysing of pollution event in Lille - urban area and Dunkerque - industrial area. We compared ground- based measurements with CALIPSO measurements. The CALIPSO level 2 aerosol records are more useful because the extinction coefficient is available. We use the extinction coefficient profiles which are provided by CALIPSO to depict the vertical structure of the aerosol properties. The combination of ground- based measurements of PM2.5, aerosol optical thickness (AOT's) obtained by Aeronet network data and CALIOP data enhances the possibilities of studying transport pathway of aerosol in the atmosphere and aerosol optical properties (aerosol extinction coefficient, aerosol optical depth, atmosphere transparency). The linear relationship between AOT _CALIPSO and AOT _ Aeronet network shows a slop of 0.4 in north of France. Moreover, we observed the good relationship between PM2.5 and AOT by CALIPSO profiles with a slope of 57.59 and correlation coefficient of 0.75 over France.

  4. 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

  5. Aerosol Best Estimate Value-Added Product

    SciTech Connect

    Flynn, C; Turner, D; Koontz, A; Chand, D; Sivaraman, C

    2012-07-19

    The objective of the Aerosol Best Estimate (AEROSOLBE) value-added product (VAP) is to provide vertical profiles of aerosol extinction, single scatter albedo, asymmetry parameter, and Angstroem exponents for the atmospheric column above the Central Facility at the ARM Southern Great Plains (SGP) site. We expect that AEROSOLBE will provide nearly continuous estimates of aerosol optical properties under a range of conditions (clear, broken clouds, overcast clouds, etc.). The primary requirement of this VAP was to provide an aerosol data set as continuous as possible in both time and height for the Broadband Heating Rate Profile (BBHRP) VAP in order to provide a structure for the comprehensive assessment of our ability to model atmospheric radiative transfer for all conditions. Even though BBHRP has been completed, AEROSOLBE results are very valuable for environmental, atmospheric, and climate research.

  6. Mass Extinctions Past and Present.

    ERIC Educational Resources Information Center

    Allmon, Warren Douglas

    1987-01-01

    Discusses some parallels that seem to exist between mass extinction recognizable in the geologic record and the impending extinction of a significant proportion of the earth's species due largely to tropical deforestation. Describes some recent theories of causal factors and periodicities in mass extinction. (Author/TW)

  7. Seasonality of Aerosols the Southeastern United States

    NASA Astrophysics Data System (ADS)

    Ford, B. J.; Heald, C. L.

    2012-12-01

    Previous studies have suggested that increases in atmospheric aerosols of biogenic origin may have caused regional cooling over the southeastern United States in recent decades. Understanding the sources and behaviors of these aerosols is important for determining their role in a changing climate and managing their air quality impacts. In this study, we investigate the strong seasonality in aerosol optical depth (AOD) observed by MODIS, MISR, and CALIOP instruments over the southeastern United States and show that this is not simulated by a chemical transport model (GEOS-Chem). However, the model does reproduce surface PM 2.5 concentrations in the region as reported by the IMPROVE and Southeastern Aerosol Research and Characterization (SEARCH) networks, as well as the muted seasonality of these concentrations. In addition, these surface measurements show that organic aerosol makes up a small fraction of total PM 2.5 and has relatively little seasonality, which calls into question the importance of biogenic aerosol as a driver for climate change in the region. Sounding profiles and ground observations of relative humidity suggest that the magnitude of seasonality in AOD cannot be explained by seasonal differences in the hygroscopic growth of aerosols. CALIOP measurements of the vertical profile of aerosol extinction confirm that the likely reconciliation of the differences in seasonality between the surface PM 2.5 and AOD observations is the formation of aerosol aloft, a process not captured by the model. These findings provide initial insights for the Southern Oxidant and Aerosol Study (SOAS) campaign in 2013 which aims to investigate the anthropogenic influence on biogenic aerosol formation in the Southeastern US and elucidate the impact on regional climate and air quality.

  8. ENCAPSULATED AEROSOLS

    DTIC Science & Technology

    acetate, polymerized rapidly and produced some polymer film encapsulation of the aerosol droplets. A two-stage microcapsule generator was designed...encapsulating material, the generator also produced microcapsules of dibutyl phosphite in polyethylene, nitrocellulose, and natural rubber.

  9. Information Retrieval from SAGE II and MFRSR Multi-Spectral Extinction Measurements

    NASA Technical Reports Server (NTRS)

    Lacis, Andrew A.; Hansen, James E. (Technical Monitor)

    2001-01-01

    Direct beam spectral extinction measurements of solar radiation contain important information on atmospheric composition in a form that is essentially free from multiple scattering contributions that otherwise tend to complicate the data analysis and information retrieval. Such direct beam extinction measurements are available from the solar occultation satellite-based measurements made by the Stratospheric and Aerosol Gas Experiment (SAGE II) instrument and by ground-based Multi-Filter Shadowband Radiometers (MFRSRs). The SAGE II data provide cross-sectional slices of the atmosphere twice per orbit at seven wavelengths between 385 and 1020 nm with approximately 1 km vertical resolution, while the MFRSR data provide atmospheric column measurements at six wavelengths between 415 and 940 nm but at one minute time intervals. We apply the same retrieval technique of simultaneous least-squares fit to the observed spectral extinctions to retrieve aerosol optical depth, effective radius and variance, and ozone, nitrogen dioxide, and water vapor amounts from the SAGE II and MFRSR measurements. The retrieval technique utilizes a physical model approach based on laboratory measurements of ozone and nitrogen dioxide extinction, line-by-line and numerical k-distribution calculations for water vapor absorption, and Mie scattering constraints on aerosol spectral extinction properties. The SAGE II measurements have the advantage of being self-calibrating in that deep space provides an effective zero point for the relative spectral extinctions. The MFRSR measurements require periodic clear-day Langley regression calibration events to maintain accurate knowledge of instrument calibration.

  10. Passive Detection of Biological Aerosols in the Atmosphere with a Fourier Transform Instrument (FTIR)—the Results of the Measurements in the Laboratory and in the Field

    NASA Astrophysics Data System (ADS)

    Błęcka, M. I.; Rataj, M.; Szymański, G.

    2012-06-01

    Fourier Transform Infrared Radiation (FTIR) spectroscopy is one of the most powerful methods for the detection of gaseous constituents, aerosols, and dust in planetary atmospheres. Infrared spectroscopy plays an important role in searching for biomarkers, organics and biological substances in the Universe. The possibility of detection and identifications with FTIR spectrometer of bio-aerosol spores ( Bacillus atrophaeus var. globigii=BG) in the atmosphere is discussed in this paper. We describe the results of initial spectral measurements performed in the laboratory and in the field. The purpose of these experiments was to detect and to identify bio-aerosol spores in two conditions: 1) In a closed chamber where the thermal contrast between the background and aerosols was large, and 2) In open air where the thermal contrast between the background and aerosols was small. The extinction spectrum of BG spores was deduced by comparing our measurements with models, and other measurements known from the literature. Our theoretical and experimental studies indicate that, during passive remote sensing measurements, it is difficult—but possible to detect and to identify bio-aerosol clouds by their spectral signatures. The simple spectral analysis described in the paper can be useful for the detection of various kinds of trace aerosols—not only in the Earth's atmosphere, but also during planetary missions in the environments of other astronomical objects such as planets, comets etc. We expect that the interpretation of data from spectrometric sounding of Venus and Mars during the current missions Mars and Venus Express, and later during the Rosetta mission will benefit from our experimental work and numerical modelling.

  11. Determination of trace metals in atmospheric aerosols with a heavy matrix of cellulose by microwave digestion-inductively coupled plasma mass spectroscopy

    NASA Astrophysics Data System (ADS)

    Yang, Karl X.; Swami, Kamal; Husain, Liaquat

    2002-01-01

    A microwave digestion method followed by inductively coupled plasma mass spectrometric (ICP-MS) analysis was developed to determine trace metal concentrations in atmospheric aerosol samples with a heavy matrix of cellulose material. A combination of HF-HNO 3-H 2O 2-H 3BO 3 was used for digestion. The background spectral features contributed by the matrix elements were studied. In particular, spectral and non-spectral interference caused by B and F were investigated. Detection limits of V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Se, Cd, Sb and Pb were determined in the presence of various amounts of matrix elements. In general, the detection limits of most elements degraded with an increase in B and F. Vanadium (V) suffered most due to severe spectral interference from 11B 40Ar + and/or 19F 16O 16O. The concentrations of elements in filter paper matrix blanks were measured. An NIST standard (urban particulate matter, 1648), as well as real world atmospheric aerosol samples from Whiteface Mountain, NY, and from Mayville, NY were pressed into pellets with a great amount of cellulose filter material and digested, and the concentrations of trace metals were determined. For the NIST standard, the recoveries of V, Mn, Fe, Co, Ni, Cu, Zn, Cd, As, Sb and Pb were over 90%, while 77 and 70% for Cr and Se, respectively. For the atmospheric aerosol samples from Whiteface Mountain and Mayville, NY, only the values of Fe, Se, As, Sb and Zn could be compared with those obtained through instrumental neutron activation analysis, and the agreement was within ±10%.

  12. Development of a laser-induced breakdown spectroscopy instrument for detection and classification of single-particle aerosols in real-time

    NASA Astrophysics Data System (ADS)

    Tjärnhage, Torbjörn; Gradmark, Per-Åke; Larsson, Anders; Mohammed, Abdelsalam; Landström, Lars; Sagerfors, Eva; Jonsson, Per; Kullander, Fredrik; Andersson, Magnus

    2013-06-01

    Detection of aerosolized biological warfare agents by means of LIBS commonly operate with pulsed lasers running at constant repetition rate, resulting in very low hit rates. In this paper, we present a prototype where the LIBS laser is only fired if a particle is expected in the focal zone. A significantly improved hit rate for detection and classification of μm sized single particles in real-time is achieved. Hit rates of 40% and 70% for NaCl particles of sizes 3 and 7.0 μm, respectively, can be reached in triggered configuration, as compared to 1% and 2% when the laser is un-triggered.

  13. Neuronal circuits of fear extinction.

    PubMed

    Herry, Cyril; Ferraguti, Francesco; Singewald, Nicolas; Letzkus, Johannes J; Ehrlich, Ingrid; Lüthi, Andreas

    2010-02-01

    Fear extinction is a form of inhibitory learning that allows for the adaptive control of conditioned fear responses. Although fear extinction is an active learning process that eventually leads to the formation of a consolidated extinction memory, it is a fragile behavioural state. Fear responses can recover spontaneously or subsequent to environmental influences, such as context changes or stress. Understanding the neuronal substrates of fear extinction is of tremendous clinical relevance, as extinction is the cornerstone of psychological therapy of several anxiety disorders and because the relapse of maladaptative fear and anxiety is a major clinical problem. Recent research has begun to shed light on the molecular and cellular processes underlying fear extinction. In particular, the acquisition, consolidation and expression of extinction memories are thought to be mediated by highly specific neuronal circuits embedded in a large-scale brain network including the amygdala, prefrontal cortex, hippocampus and brain stem. Moreover, recent findings indicate that the neuronal circuitry of extinction is developmentally regulated. Here, we review emerging concepts of the neuronal circuitry of fear extinction, and highlight novel findings suggesting that the fragile phenomenon of extinction can be converted into a permanent erasure of fear memories. Finally, we discuss how research on genetic animal models of impaired extinction can further our understanding of the molecular and genetic bases of human anxiety disorders.

  14. Pulsar extinction. [astrophysics

    NASA Technical Reports Server (NTRS)

    Sturrock, P. A.; Baker, K.; Turk, J. S.

    1975-01-01

    Radio emission from pulsars, attributed to an instability associated with the creation of electron-positron pairs from gamma rays was investigated. The condition for pair creation therefore lead to an extinction condition. The relevant physical processes were analyzed in the context of a mathematical model, according to which radiation originated at the polar caps and magnetic field lines changed from a closed configuration to an open configuration at the force balance or corotation radius.

  15. Extinction in SC galaxies

    NASA Astrophysics Data System (ADS)

    Giovanelli, Riccardo; Haynes, Martha P.; Salzer, John J.; Wegner, Gary; da Costa, Luiz N.; Freudling, Wolfram

    1994-06-01

    We analyze the photometric properties of a sample of Sbc-Sc galaxies with known redshifts, single-dish H I profiles, and Charge Coupled Device (CCD) I band images. We derive laws that relate the measured isophotal radius at muI = 23.5, magnitude, scale length, and H I flux to the face-on aspect. We find spiral galaxies to be substantially less transparent than suggested in most previous determinations, but not as opaque as claimed by Valentijn (1990). Regions in the disk farther than two or three scale lengths from the center are close to completely transparent. In addition to statistically derived relations for the inclination dependence of photometric parameters, we present the results of a modeling exercise that utilizes the 'triplex' model of Disney et al. (1989) to obtain upper limits of the disk opacity. Within the framework of that model, and with qualitative consideration of the effects of scattering on extinction, we estimate late spiral disks at I band to have central optical depths tauI(0) less than 5 and dust absorbing layers with scale heights on the order of half that of the stellar component or less. We discuss our results in light of previous determinations of internal extinction relations and point out the substantial impact of internal extinction on the scatter of the Tully-Fisher relation. We also find that the visual diameters by which large catalogs are constructed (UGC, ESO-Uppsala) are nearly proportional to face-on isophotal diameters.

  16. A method to quantify organic functional groups and inorganic compounds in ambient aerosols using attenuated total reflectance FTIR spectroscopy and multivariate chemometric techniques

    NASA Astrophysics Data System (ADS)

    Coury, Charity; Dillner, Ann M.

    An attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopic technique and a multivariate calibration method were developed to quantify ambient aerosol organic functional groups and inorganic compounds. These methods were applied to size-resolved particulate matter samples collected in winter and summer of 2004 at three sites: a downtown Phoenix, Arizona location, a rural site near Phoenix, and an urban fringe site between the urban and rural site. Ten organic compound classes, including four classes which contain a carbonyl functional group, and three inorganic species were identified in the ambient samples. A partial least squares calibration was developed and applied to the ambient spectra, and 13 functional groups related to organic compounds (aliphatic and aromatic CH, methylene, methyl, alkene, aldehydes/ketones, carboxylic acids, esters/lactones, acid anhydrides, carbohydrate hydroxyl and ethers, amino acids, and amines) as well as ammonium sulfate and ammonium nitrate were quantified. Comparison of the sum of the mass measured by the ATR-FTIR technique and gravimetric mass indicates that this method can quantify nearly all of the aerosol mass on sub-micrometer size-segregated samples. Analysis of sample results shows that differences in organic functional group and inorganic compound concentrations at the three sampling sites can be measured with these methods. Future work will analyze the quantified data from these three sites in detail.

  17. Aerosol Measurements by the Globally Distributed Micro Pulse Lidar Network

    NASA Technical Reports Server (NTRS)

    Spinhirne, James; Welton, Judd; Campbell, James; Berkoff, Tim; Starr, David (Technical Monitor)

    2001-01-01

    Full time measurements of the vertical distribution of aerosol are now being acquired at a number of globally distributed MP (micro pulse) lidar sites. The MP lidar systems provide full time profiling of all significant cloud and aerosol to the limit of signal attenuation from compact, eye safe instruments. There are currently eight sites in operation and over a dozen planned. At all sited there are also passive aerosol and radiation measurements supporting the lidar data. Four of the installations are at Atmospheric Radiation Measurement program sites. The network operation includes instrument operation and calibration and the processing of aerosol measurements with standard retrievals and data products from the network sites. Data products include optical thickness and extinction cross section profiles. Application of data is to supplement satellite aerosol measurements and to provide a climatology of the height distribution of aerosol. The height distribution of aerosol is important for aerosol transport and the direct scattering and absorption of shortwave radiation in the atmosphere. Current satellite and other data already provide a great amount of information on aerosol distribution, but no passive technique can adequately resolve the height profile of aerosol. The Geoscience Laser Altimeter System (GLAS) is an orbital lidar to be launched in early 2002. GLAS will provide global measurements of the height distribution of aerosol. The MP lidar network will provide ground truth and analysis support for GLAS and other NASA Earth Observing System data. The instruments, sites, calibration procedures and standard data product algorithms for the MPL network will be described.

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

    NASA Astrophysics Data System (ADS)

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

    2003-12-01

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

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

    SciTech Connect

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

    2011-07-06

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

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

    NASA Astrophysics Data System (ADS)

    Brock, Charles; Wagner, Nick; Gordon, Timothy

    2016-04-01

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

  1. Revisiting Aerosol Effects in Global Climate Models Using an Aerosol Lidar Simulator

    NASA Astrophysics Data System (ADS)

    Ma, P. L.; Chepfer, H.; Winker, D. M.; Ghan, S.; Rasch, P. J.

    2015-12-01

    Aerosol effects are considered a major source of uncertainty in global climate models and the direct and indirect radiative forcings have strong model dependency. These forcings are routinely evaluated (and calibrated) against observations, among them satellite retrievals are greatly used for their near-global coverage. However, the forcings calculated from model output are not directly comparable with those computed from satellite retrievals since sampling and algorithmic differences (such as cloud screening, noise reduction, and retrieval) between models and observations are not accounted for. It is our hypothesis that the conventional model validation procedures for comparing satellite observations and model simulations can mislead model development and introduce biases. Hence, we have developed an aerosol lidar simulator for global climate models that simulates the CALIOP lidar signal at 532nm. The simulator uses the same algorithms as those used to produce the "GCM-oriented CALIPSO Aerosol Product" to (1) objectively sample lidar signal profiles; and (2) derive aerosol fields (e.g., extinction profile, aerosol type, etc) from lidar signals. This allows us to sample and derive aerosol fields in the model and real atmosphere in identical ways. Using the Department of Energy's ACME model simulations, we found that the simulator-retrieved aerosol distribution and aerosol-cloud interactions are significantly different from those computed from conventional approaches, and that the model is much closer to satellite estimates than previously believed.

  2. Tropospheric Aerosols

    NASA Astrophysics Data System (ADS)

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

    2003-12-01

    It is widely believed that "On a clear day you can see forever," as proclaimed in the 1965 Broadway musical of the same name. While an admittedly beautiful thought, we all know that this concept is only figurative. Aside from Earth's curvature and Rayleigh scattering by air molecules, aerosols - colloidal suspensions of solid or liquid particles in a gas - limit our vision. Even on the clearest day, there are billions of aerosol particles per cubic meter of air.Atmospheric aerosols are commonly referred to as smoke, dust, haze, and smog, terms that are loosely reflective of their origin and composition. Aerosol particles have arisen naturally for eons from sea spray, volcanic emissions, wind entrainment of mineral dust, wildfires, and gas-to-particle conversion of hydrocarbons from plants and dimethylsulfide from the oceans. However, over the industrial period, the natural background aerosol has been greatly augmented by anthropogenic contributions, i.e., those produced by human activities. One manifestation of this impact is reduced visibility (Figure 1). Thus, perhaps more than in other realms of geochemistry, when considering the composition of the troposphere one must consider the effects of these activities. The atmosphere has become a reservoir for vast quantities of anthropogenic emissions that exert important perturbations on it and on the planetary ecosystem in general. Consequently, much recent research focuses on the effects of human activities on the atmosphere and, through them, on the environment and Earth's climate. For these reasons consideration of the geochemistry of the atmosphere, and of atmospheric aerosols in particular, must include the effects of human activities. (201K)Figure 1. Impairment of visibility by aerosols. Photographs at Yosemite National Park, California, USA. (a) Low aerosol concentration (particulate matter of aerodynamic diameter less than 2.5 μm, PM2.5=0.3 μg m-3; particulate matter of aerodynamic diameter less than 10

  3. Cloud identification in atmospheric trace molecule spectroscopy infrared occultation measurements.

    PubMed

    Kahn, Brian H; Eldering, Annmarie; Irion, Fredrick W; Mills, Franklin P; Sen, Bhaswar; Gunson, Michael R

    2002-05-20

    High-resolution infrared nongas absorption spectra derived from the Atmospheric Trace Molecule Spectroscopy (ATMOS) experiment are analyzed for evidence of the presence of cirrus clouds. Several nonspherical ice extinction models based on realistic size distributions and crystal habits along with a stratospheric sulfate aerosol model are fit to the spectra, and comparisons are made with different model combinations. Nonspherical ice models often fit observed transmission spectra better than a spherical Mie ice model, and some discrimination among nonspherical models is noted. The ATMOS lines of sight for eight occultations are superimposed on coincident geostationary satellite infrared imagery, and brightness temperatures along the lines of sight are compared with retrieved vertical temperature profiles. With these comparisons, studies of two cases of clear sky, three cases of opaque cirrus, and three cases of patchy cirrus are discussed.

  4. Composition of Polar Stratospheric Clouds from Infrared Spectroscopy

    NASA Technical Reports Server (NTRS)

    Tolbert, M. A.; Anthony, S. E.; Disselkamp, R.; Toon, O. B.; Condon, Estelle P. (Technical Monitor)

    1995-01-01

    Heterogeneous reactions on polar stratospheric clouds (PSCs) have recently been implicated in Arctic and Antarctic ozone destruction. Although the chemistry is well documented, the composition of the clouds remains uncertain. The most common PSCs (type I) are thought to be composed of HNO3/H2O mixtures. Although the exact process is not clear, type I PSCs are believed to nucleate on preexisting stratospheric sulfate aerosols (SSAs) composed of sulfuric acid and water. We are using infrared spectroscopy to study the composition and formation mechanism of type I PSCs. In the laboratory, we have used FTIR spectroscopy to probe the composition and phase of H2SO4/HNO3/H2O aerosols under winter polar stratospheric conditions. We have also used recently measured infrared optical constants for HNO3/H2O mixtures to analyze solar infrared extinction measurements of type I PSCs obtained in September 1987 over Antarctica. The results of these studies will be discussed in the context of current theories for polar stratospheric clouds formation.

  5. Spectral signatures of polar stratospheric clouds and sulfate aerosol

    SciTech Connect

    Massie, S.T.; Bailey, P.L.; Gille, J.C.; Lee, E.C.; Mergenthaler, J.L.; Roche, A.E.; Kumer, J.B.; Fishbein, E.F.; Waters, J.W.; Lahoz, W.A.

    1994-10-15

    Multiwavelength observations of Antarctic and midlatitude aerosol by the Cryogenic Limb Array Etalon Spectrometer (CLAES) experiment on the Upper Atmosphere Research Satellite are used to demonstrate a technique that identifies the location of polar stratospheric clouds. The technique discussed uses the normalized area of the triangle formed by the aerosol extinctions at 925, 1257, and 1605 cm{sup {minus}1} (10.8, 8.0, and 6.2 {mu}m) to derive a spectral aerosol measure M of the aerosol spectrum. Mie calculations for spherical particles and T-matrix calculations for spheroidal particles are used to generate theoretical spectral extinction curves for sulfate and polar stratospheric cloud particles. The values of the spectral aerosol measure M for the sulfate and polar stratospheric cloud particles are shown to be different. Aerosol extinction data, corresponding to temperatures between 180 and 220 K at a pressure of 46 hPa (near 21-km altitude) for 18 August 1992, are used to demonstrate the technique. Thermodynamic calculations, based upon frost-point calculation and laboratory phase-equilibrium studies of nitric acid trihydrate, are used to predict the location of nitric acid trihydrate cloud particles. 47 refs., 22 figs., 3 tabs.

  6. Spectral signatures of polar stratospheric clouds and sulfate aerosol

    NASA Technical Reports Server (NTRS)

    Massie, S. T.; Bailey, P. L.; Gille, J. C.; Lee, E. C.; Mergenthaler, J. L.; Roche, A. E.; Kumer, J. B.; Fishbein, E. F.; Waters, J. W.; Lahoz, W. A.

    1994-01-01

    Multiwavelength observations of Antarctic and midlatitude aerosol by the Cryogenic Limb Array Etalon Spectrometer (CLAES) experiment on the Upper Atmosphere Research Satellite (UARS) are used to demonstrate a technique that identifies the location of polar stratospheric clouds. The technique discussed uses the normalized area of the triangle formed by the aerosol extinctions at 925, 1257, and 1605/cm (10.8, 8.0, and 6.2 micrometers) to derive a spectral aerosol measure M of the aerosol spectrum. Mie calculations for spherical particles and T-matrix calculations for spheriodal particles are used to generate theoretical spectral extinction curves for sulfate and polar stratospheric cloud particles. The values of the spectral aerosol measure M for the sulfate and polar stratospheric cloud particles are shown to be different. Aerosol extinction data, corresponding to temperatures between 180 and 220 K at a pressure of 46 hPa (near 21-km altitude) for 18 August 1992, are used to demonstrate the technique. Thermodynamic calculations, based upon frost-point calculations and laboratory phase-equilibrium studies of nitric acid trihydrate, are used to predict the location of nitric acid trihydrate cloud particles.

  7. Stratospheric aerosols from the Sarychev volcano eruption in the 2009 Arctic summer

    NASA Astrophysics Data System (ADS)

    Jégou, F.; Berthet, G.; Brogniez, C.; Renard, J.-B.; François, P.; Haywood, J. M.; Jones, A.; Bourgeois, Q.; Lurton, T.; Auriol, F.; Godin-Beekmann, S.; Guimbaud, C.; Krysztofiak, G.; Gaubicher, B.; Chartier, M.; Clarisse, L.; Clerbaux, C.; Balois, J. Y.; Verwaerde, C.

    2013-02-01

    Aerosols from the Sarychev volcano eruption (Kuril Islands, northeast of Japan) were observed in the Arctic lower stratosphere a few days after the strongest SO2 injection which occurred on 15 and 16 June 2009. From the observations provided by the Infrared Atmospheric Sounding Interferometer (IASI) an estimated 0.9 Tg of sulphur dioxide was injected into the Upper Troposphere and Lower Stratosphere (UTLS). The resultant stratospheric sulphate aerosols were detected by the Optical Spectrograph and Infrared Imaging System (OSIRIS) limb sounder and by the Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP) satellite instruments. By the first week of July the aerosol plume had spread out over the entire Arctic region. The Sarychev-induced stratospheric aerosol over the Kiruna region (north of Sweden) was measured by the Stratospheric and Tropospheric Aerosol Counter (STAC) during eight balloon flights planned in August and September 2009. During this balloon campaign the Micro RADIomètre BALlon (MicroRADIBAL) and the Spectroscopie d'Absorption Lunaire pour l'Observation des Minoritaires Ozone et NOx (SALOMON) remote-sensing instruments also observed these aerosols. Aerosol concentrations returned to near-background levels by spring 2010. The effective radius, the Surface Area Density (SAD), the aerosol extinction, and the total sulphur mass from STAC in situ measurements are enhanced with mean values in the range 0.15-0.21 μm, 5.5-14.7 μm2 cm-3, 5.5-29.5×10-4 km-1, and 4.9-12.6×10-10 kg [S] kg-1 [air], respectively, between 14 km and 18 km. The observed and modelled e-folding time of sulphate aerosols from the Sarychev eruption is around 70-80 days, a value much shorter than the 12-14 months calculated for aerosols from the 1991 eruption of Mt. Pinatubo. The OSIRIS stratospheric Aerosol Optical Depth (AOD) at 750 nm is enhanced by a factor of 6 with a value of 0.02 in late July compared to 0.0035 before the eruption. The HadGEM2 and MIMOSA model outputs

  8. Stratospheric aerosols from the Sarychev volcano eruption in the 2009 Arctic summer

    NASA Astrophysics Data System (ADS)

    Jégou, F.; Berthet, G.; Brogniez, C.; Renard, J.-B.; François, P.; Haywood, J. M.; Jones, A.; Bourgeois, Q.; Lurton, T.; Auriol, F.; Godin-Beekmann, S.; Guimbaud, C.; Krysztofiak, G.; Gaubicher, B.; Chartier, M.; Clarisse, L.; Clerbaux, C.; Balois, J. Y.; Verwaerde, C.; Daugeron, D.

    2013-07-01

    Aerosols from the Sarychev volcano eruption (Kuril Islands, northeast of Japan) were observed in the Arctic lower stratosphere a few days after the strongest SO2 injection which occurred on 15 and 16 June 2009. From the observations provided by the Infrared Atmospheric Sounding Interferometer (IASI) an estimated 0.9 Tg of sulphur dioxide was injected into the upper troposphere and lower stratosphere (UTLS). The resultant stratospheric sulphate aerosols were detected from satellites by the Optical Spectrograph and Infrared Imaging System (OSIRIS) limb sounder and by the Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP) and from the surface by the Network for the Detection of Atmospheric Composition Changes (NDACC) lidar deployed at OHP (Observatoire de Haute-Provence, France). By the first week of July the aerosol plume had spread out over the entire Arctic region. The Sarychev-induced stratospheric aerosol over the Kiruna region (north of Sweden) was measured by the Stratospheric and Tropospheric Aerosol Counter (STAC) during eight balloon flights planned in August and September 2009. During this balloon campaign the Micro Radiomètre Ballon (MicroRADIBAL) and the Spectroscopie d'Absorption Lunaire pour l'Observation des Minoritaires Ozone et NOx (SALOMON) remote-sensing instruments also observed these aerosols. Aerosol concentrations returned to near-background levels by spring 2010. The effective radius, the surface area density (SAD), the aerosol extinction, and the total sulphur mass from STAC in situ measurements are enhanced with mean values in the range 0.15-0.21 μm, 5.5-14.7 μm2 cm-3, 5.5-29.5 × 10-4 km-1, and 4.9-12.6 × 10-10 kg[S] kg-1[air], respectively, between 14 km and 18 km. The observed and modelled e-folding time of sulphate aerosols from the Sarychev eruption is around 70-80 days, a value much shorter than the 12-14 months calculated for aerosols from the 1991 eruption of Mt Pinatubo. The OSIRIS stratospheric aerosol optical depth (AOD

  9. Endangered and Extinct Radioactivity

    NASA Astrophysics Data System (ADS)

    Leising, M. D.

    1993-07-01

    Gamma ray spectroscopy holds great promise for probing nucleosynthesis in individual nucleosynthesis events, via observations of short-lived radioactivity, and for measuring global galactic nucleosynthesis today with detections of longer-lived radioactivity. Many of the astrophysical issues addressed by these observations are precisely those that must be understood in order to interpret observations of extinct radioactivity in meteorites. It was somewhat surprising that the former case was realized first for a Type II supernova, when both 56Co [1] and 57Co [2] were detected in SN 1987A. These provide unprecedented constraints on models of Type II explosions. Live 26Al in the galaxy might come from Type II supernovae and their progenitors, and if this is eventually shown to be the case, can constrain massive star evolution, supernova nucleosynthesis, the galactic Type II supernova rate, and even models of the chemical evolution of the galaxy [3]. Titanium-44 is produced primarily in the alpha-rich freezeout from nuclear statistical equilibrium, possibly in Type Ia [4] and almost certainly in Type II supernovae [5]. The galactic recurrence time of these events is comparable to the 44Ti lifetime, so we expect to be able to see at most a few otherwise unseen 44Ti remnants at any given time. No such remnants have been detected yet [6]. Very simple arguments lead to the expectation that about 4 x 10^-4 M(sub)solar mass of 44Ca are produced per century. The product of the supernova frequency times the 44Ti yield per event must equal this number. Even assuming that only the latest event would be seen, rates in excess of 2 century^-1 are ruled out at >=99% confidence by the gamma ray limits. Only rates less than 0.3 century^-1 are acceptable at >5% confidence, and this means that the yield per event must be >10^-3 M(sub)solar mass to produce the requisite 44Ca. Rates this low are incompatible with current estimates for Type II supernovae and yields this high are also very

  10. Seasonal variability of tropospheric aerosols in Rome

    NASA Astrophysics Data System (ADS)

    Ciardini, Virginia; Di Iorio, Tatiana; Di Liberto, Luca; Tirelli, Cecilia; Casasanta, Giampietro; di Sarra, Alcide; Fiocco, Giorgio; Fuà, Daniele; Cacciani, Marco

    2012-11-01

    The seasonal evolution of the tropospheric aerosol vertical distribution and of its optical properties is investigated using lidar and multi-filter rotating shadow-band radiometer (MFRSR) measurements collected throughout the period 2006-2009 in the urban environment of Rome. The evolution of the aerosol distribution is studied also in relation to long range transport of dust. Hybrid Single-Particle Lagrangian Integrated Trajectory model backward trajectories are used to identify possible aerosol sources in remote regions. Aerosol optical depth at 500 nm, τ, and Ångström exponent, α, are derived from MFRSR measurements. The Ångström exponent generally displays relatively high values, indicating the predominance of fine particle over the entire column. The average optical depth at 500 nm and Ångström exponent over the whole period are 0.18 ± 0.09 and 1.12 ± 0.39, respectively. Cases affected by Saharan dust (class 1) are separated from those not influenced by dust (class 0) by using backward trajectories. The average values of τ and α are 0.17 ± 0.08 and 1.17 ± 0.36 for class 0, respectively, and 0.22 ± 0.09 and 0.95 ± 0.46 for class 1. About 214 days of lidar measurements are selected for the analysis. The aerosol vertical distribution is influenced by dust events that induce a marked seasonal behaviour. Desert dust generally reaches higher altitudes than other aerosol types; the maxima altitudes are observed during Spring and Summer, when the monthly average altitude exceeds 5 km. The annual average occurrence of desert dust is 27%, with maxima in Spring and in the first part of Summer. The decrease in the dust event frequency observed in winter months is mainly linked to the seasonal behaviour of the synoptic circulation in the Mediterranean. According to the back-trajectories aerosols are primarily observed below 3 km altitude throughout the year when classified as not affected by desert dust. The extinction coefficient vertical profiles for the

  11. MEST- avoid next extinction

    NASA Astrophysics Data System (ADS)

    Cao, Dayong

    2012-11-01

    Asteroid 2011 AG5 will impact on Earth in 2040. (See Donald K. Yoemans, ``Asteroid 2011 AG5 - A Reality Check,'' NASA-JPL, 2012) In 2011, The author say: the dark hole will take the dark comet to impact our solar system in 20 years, and give a systemic model between the sun and its companion-dark hole to explain why were there periodicity mass extinction on earth. (see Dayong Cao, BAPS.2011.CAL.C1.7, BAPS.2011.DFD.LA.24, BAPS.2012.APR.K1.78 and BAPS.2011.APR.K1.17) The dark Asteroid 2011 AG5 (as a dark comet) is made of the dark matter which has a space-time (as frequence-amplitude square) center- a different systemic model from solar systemic model. It can asborb the space-time and wave. So it is ``dark.'' When many dark matters hit on our earth, they can break our atom structure and our genetic code to trigger the Mass Extinction. In our experiments, consciousness can change the systematic model and code by a life-informational technology. So it can change the output signals of the solar cell. (see Dayong Cao, BAPS.2011.MAR.C1.286 and BAPS.2012.MAR.P33.14) So we will develop the genetic code of lives to evolution and sublimation, will use the dark matter to change the systemic model between dark hole and sun and will avoid next extinction.

  12. A Compact Airborne High Spectral Resolution Lidar for Observations of Aerosol and Cloud Optical Properties

    NASA Technical Reports Server (NTRS)

    Hostetler, Chris A.; Hair, John W.; Cook, Anthony L.

    2002-01-01

    We are in the process of developing a nadir-viewing, aircraft-based high spectral resolution lidar (HSRL) at NASA Langley Research Center. The system is designed to measure backscatter and extinction of aerosols and tenuous clouds. The primary uses of the instrument will be to validate spaceborne aerosol and cloud observations, carry out regional process studies, and assess the predictions of chemical transport models. In this paper, we provide an overview of the instrument design and present the results of simulations showing the instrument's capability to accurately measure extinction and extinction-to-backscatter ratio.

  13. Aerosol Climate Time Series in ESA Aerosol_cci

    NASA Astrophysics Data System (ADS)

    Popp, Thomas; de Leeuw, Gerrit; Pinnock, Simon

    2016-04-01

    Within the ESA Climate Change Initiative (CCI) Aerosol_cci (2010 - 2017) conducts intensive work to improve algorithms for the retrieval of aerosol information from European sensors. Meanwhile, full mission time series of 2 GCOS-required aerosol parameters are completely validated and released: Aerosol Optical Depth (AOD) from dual view ATSR-2 / AATSR radiometers (3 algorithms, 1995 - 2012), and stratospheric extinction profiles from star occultation GOMOS spectrometer (2002 - 2012). Additionally, a 35-year multi-sensor time series of the qualitative Absorbing Aerosol Index (AAI) together with sensitivity information and an AAI model simulator is available. Complementary aerosol properties requested by GCOS are in a "round robin" phase, where various algorithms are inter-compared: fine mode AOD, mineral dust AOD (from the thermal IASI spectrometer, but also from ATSR instruments and the POLDER sensor), absorption information and aerosol layer height. As a quasi-reference for validation in few selected regions with sparse ground-based observations the multi-pixel GRASP algorithm for the POLDER instrument is used. Validation of first dataset versions (vs. AERONET, MAN) and inter-comparison to other satellite datasets (MODIS, MISR, SeaWIFS) proved the high quality of the available datasets comparable to other satellite retrievals and revealed needs for algorithm improvement (for example for higher AOD values) which were taken into account for a reprocessing. The datasets contain pixel level uncertainty estimates which were also validated and improved in the reprocessing. For the three ATSR algorithms the use of an ensemble method was tested. The paper will summarize and discuss the status of dataset reprocessing and validation. The focus will be on the ATSR, GOMOS and IASI datasets. Pixel level uncertainties validation will be summarized and discussed including unknown components and their potential usefulness and limitations. Opportunities for time series extension

  14. 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.

  15. Volcanic Aerosols from Satellites: Current and Emerging Capabilities

    NASA Astrophysics Data System (ADS)

    Bhartia, P. K.; McCormick, M. P.; Loughman, R. P.

    2015-12-01

    There are 5 instruments currently operating in space with capability to measure stratospheric aerosols. Two of these are lidar backscatter instruments (CALIOP & ISS/CATS) that provide high vertical resolution, day/night coverage, and polarization information to separate ice clouds from sulfate aerosols. Two are limb scattering instruments (OSIRIS & OMPS-LP) with high sensitivity to aerosols and provide extensive spatial coverage of the sunlit globe. And a Canadian solar occultation instrument (ACE-MAESTRO) measures aerosol extinction twice per orbit. Next year we are expecting the launch of the SAGE III instrument on ISS with capability to measure aerosol extinction and Angstrom Exponent (AE) at multiple wavelengths by solar and lunar occultation techniques. It also has limb scattering capability to provide spatial coverage between solar occultations. The 51.6˚ inclination of the ISS orbit will allow SAGE III to measure aerosol scattering across the gobe for a wide range of scattering angles. Therefore, ISS SAGE III has the capability to provide vertically resolved information about a wide variety of aerosol properties, potentially including aerosol extinction, size distribution, refractive index, and particle shape parameters, similar to the one provided by the ground-based almucantar technique. In our talk we will focus primarily on the synergy between the OMPS LP instrument that has been flying on the Suomi NPP satellite since October 2011 and ISS SAGE III. We will show how these measurements can be combined together to capture spatial and temporal evolution of aerosols and ozone in large volcanic plumes to validate models and to support field campaigns.

  16. Periodicity in marine extinction events

    NASA Technical Reports Server (NTRS)

    Sepkoski, J. John, Jr.; Raup, David M.

    1986-01-01

    The periodicity of extinction events is examined in detail. In particular, the temporal distribution of specific, identifiable extinction events is analyzed. The nature and limitations of the data base on the global fossil record is discussed in order to establish limits of resolution in statistical analyses. Peaks in extinction intensity which appear to differ significantly from background levels are considered, and new analyses of the temporal distribution of these peaks are presented. Finally, some possible causes of periodicity and of interdependence among extinction events over the last quarter billion years of earth history are examined.

  17. The impact of mass extinctions

    NASA Technical Reports Server (NTRS)

    Flessa, Karl W.

    1988-01-01

    In the years since Snowbird an explosive growth of research on the patterns, causes, and consequences of extinction was seen. The fossil record of extinction is better known, stratigraphic sections were scrutinized in great detail, and additional markers of environmental change were discovered in the rock record. However flawed, the fossil record is the only record that exists of natural extinction. Compilations from the primary literature contain a faint periodic signal: the extinctions of the past 250 my may be regulary spaced. The reality of the periodicity remains a subject for debate. The implications of periodicity are so profound that the debate is sure to continue. The greater precision from stratigraphic sections spanning extinction events has yet to resolve controversies concerning the rates at which extinctions occurred. Some sections seem to record sudden terminations, while others suggest gradual or steplike environmental deterioration. Unfortunately, the manner in which the strata record extinctions and compile stratigraphic ranges makes a strictly literal reading of the fossil record inadvisable. Much progress was made in the study of mass extinctions. The issues are more sharply defined but they are not fully resolved. Scenarios should look back to the phenomena they purport to explain - not just an iridium-rich layer, but the complex fabric of a mass extinction.

  18. Overview of the Cumulus Humilis Aerosol Processing Study

    SciTech Connect

    Berg, Larry K.; Berkowitz, Carl M.; Ogren, John A.; Hostetler, Chris A.; Ferrare, Richard; Dubey, Manvendra K.; Andrews, Elizabeth; Coulter, Richard L.; Hair, John; Hubbe, John M.; Lee, Yin-Nan; Mazzoleni, Claudio; Olfert, Jason N.; Springston, Stephen R.

    2009-11-30

    The primary goal of the Cumulus Humilis Aerosol Processing Study (CHAPS) was to characterize and contrast freshly emitted aerosols below, above, and within fields of cumuli, and to study changes to the cloud microphysical structure within these same cloud fields. The CHAPS is one of very few studies that have had an Aerosol Mass Spectrometer (AMS) sampling downstream of a counter-flow virtual impactor (CVI) inlet on an aircraft, allowing the examination of the chemical composition of the nucleated aerosols within the cumuli. The results from the CHAPS will provide insights into changes in the aerosol chemical and optical properties as aerosols move through shallow cumuli downwind of a moderately sized city. Three instrument platforms were employed during the CHAPS, including the U.S. Department of Energy Gulfstream-1 aircraft, which was equipped for in situ sampling of aerosol optical and chemical properties; the NASA-Langley King Air B200, which carried the downward looking NASA Langley High Spectral Resolution Lidar (HSRL) to measure profiles of aerosol backscatter, extinction, and depolarization between the King Air and the surface; and a surface site equipped for continuous in situ measurements of aerosol properties, profiles of aerosol backscatter, and meteorological conditions including total sky cover and thermodynamic profiles of the atmosphere. In spite of record precipitation over central Oklahoma, a total of eight research flights were made by the G-1, and eighteen by the B200, including special satellite verification flights timed to coincide with NASA satellite A-Train overpasses.

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

    NASA Astrophysics Data System (ADS)

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

    2014-01-01

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

  20. The post-pinatubo evolution of stratospheric aerosol surface area density as inferred from SAGE 2

    NASA Technical Reports Server (NTRS)

    Poole, L. R.; Thomason, L. W.

    1994-01-01

    Following the eruption of Mount Pinatubo in June of 1991, the aerosol mass loading of the stratosphere increased from -1 Mt to approximately 30 Mt. This change in aerosol loading was responsible for numerous radiative and chemical changes observed within the stratosphere. As a result, the ability to quantify aerosol properties on a global basis during this period is important. Aerosol surface area density is a critical parameter in governing the rates of heterogeneous reactions, such as ClONO2 plus H2O yields HNO3 plus HOCl, which influence the stratospheric abundance of ozone. Following the eruption of Mt. Pinatubo, measurements by the Stratospheric Aerosol and Gas Experiment (SAGE 2) indicated that the stratospheric aerosol surface area density increased by as much as a factor of 100. Using SAGE 2 multi-wavelength aerosol extinction data, aerosol surface area density as well as mass are derived for the period following the eruption of Mt. Pinatubo through the present.

  1. Identifying Aerosol Type/Mixture from Aerosol Absorption Properties Using AERONET

    NASA Technical Reports Server (NTRS)

    Giles, D. M.; Holben, B. N.; Eck, T. F.; Sinyuk, A.; Dickerson, R. R.; Thompson, A. M.; Slutsker, I.; Li, Z.; Tripathi, S. N.; Singh, R. P.; Zibordi, G.

    2010-01-01

    Aerosols are generated in the atmosphere through anthropogenic and natural mechanisms. These sources have signatures in the aerosol optical and microphysical properties that can be used to identify the aerosol type/mixture. Spectral aerosol absorption information (absorption Angstrom exponent; AAE) used in conjunction with the particle size parameterization (extinction Angstrom exponent; EAE) can only identify the dominant absorbing aerosol type in the sample volume (e.g., black carbon vs. iron oxides in dust). This AAE/EAE relationship can be expanded to also identify non-absorbing aerosol types/mixtures by applying an absorption weighting. This new relationship provides improved aerosol type distinction when the magnitude of absorption is not equal (e.g, black carbon vs. sulfates). The Aerosol Robotic Network (AERONET) data provide spectral aerosol optical depth and single scattering albedo - key parameters used to determine EAE and AAE. The proposed aerosol type/mixture relationship is demonstrated using the long-term data archive acquired at AERONET sites within various source regions. The preliminary analysis has found that dust, sulfate, organic carbon, and black carbon aerosol types/mixtures can be determined from this AAE/EAE relationship when applying the absorption weighting for each available wavelength (Le., 440, 675, 870nm). Large, non-spherical dust particles absorb in the shorter wavelengths and the application of 440nm wavelength absorption weighting produced the best particle type definition. Sulfate particles scatter light efficiently and organic carbon particles are small near the source and aggregate over time to form larger less absorbing particles. Both sulfates and organic carbon showed generally better definition using the 870nm wavelength absorption weighting. Black carbon generation results from varying combustion rates from a number of sources including industrial processes and biomass burning. Cases with primarily black carbon showed

  2. Midinfrared optical properties of petroleum oil aerosols

    NASA Astrophysics Data System (ADS)

    Gurton, K. P.; Bruce, C. W.

    1994-08-01

    The mass normalized absorption and extinction coefficients were measured for fog oil aerosol at 3.4 micrometers with a combined photoacoustic and transmissometer system. An extinction spectral profile was determined over a range of infrared (IR) wavelengths from 2.7 to 4.0 micrometers by an IR scanning transmissometer. The extinction spectrum was mass normalized by referencing it to the photoacoustic portion of the experiment. A corresponding Mie calculation was conducted and compared with the above measurements. Agreement is good for the most recent optical coefficients. An extrapolation of this data to other similar petroleum products such as kerosene or diesel fuel that exhibit similar bulk absorption characteristics were briefly examined.

  3. 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.

  4. Aerosol physical properties in the stratosphere (APPS) radiometer design

    NASA Technical Reports Server (NTRS)

    Gray, C. R.; Woodin, E. A.; Anderson, T. J.; Magee, R. J.; Karthas, G. W.

    1977-01-01

    The measurement concepts and radiometer design developed to obtain earth-limb spectral radiance measurements for the Aerosol Physical Properties in the Stratosphere (APPS) measurement program are presented. The measurements made by a radiometer of this design can be inverted to yield vertical profiles of Rayleigh scatterers, ozone, nitrogen dioxide, aerosol extinction, and aerosol physical properties, including a Junge size-distribution parameter, and a real and imaginary index of refraction. The radiometer design provides the capacity for remote sensing of stratospheric constituents from space on platforms such as the space shuttle and satellites, and therefore provides for global measurements on a daily basis.

  5. Vertical Profiles of Aerosol Optical Properties Over Central Illinois and Comparison with Surface and Satellite Measurements

    NASA Technical Reports Server (NTRS)

    Sheridan P. J.; Andrews, E.; Ogren, J A.; Tackett, J. L.; Winker, D. M.

    2012-01-01

    Between June 2006 and September 2009, an instrumented light aircraft measured over 400 vertical profiles of aerosol and trace gas properties over eastern and central Illinois. The primary objectives of this program were to (1) measure the in situ aerosol properties and determine their vertical and temporal variability and (2) relate these aircraft measurements to concurrent surface and satellite measurements. Underflights of the CALIPSO satellite show reasonable agreement in a majority of retrieved profiles between aircraft-measured extinction at 532 nm (adjusted to ambient relative humidity) and CALIPSO-retrieved extinction, and suggest that routine aircraft profiling programs can be used to better understand and validate satellite retrieval algorithms. CALIPSO tended to overestimate the aerosol extinction at this location in some boundary layer flight segments when scattered or broken clouds were present, which could be related to problems with CALIPSO cloud screening methods. The in situ aircraft-collected aerosol data suggest extinction thresholds for the likelihood of aerosol layers being detected by the CALIOP lidar. These statistical data offer guidance as to the likelihood of CALIPSO's ability to retrieve aerosol extinction at various locations around the globe.

  6. Extinction and backscatter cross sections of biological materials

    NASA Astrophysics Data System (ADS)

    Thomas, M. E.; Hahn, D. V.; Carr, A. K.; Limsui, D.; Carter, C. C.; Boggs, N. T.; Jackman, J.

    2008-04-01

    Aerosol backscatter and extinction cross-sections are required to model and evaluate the performance of both active and passive detection systems. A method has been developed that begins with laboratory measurements of thin films and suspensions of biological material to obtain the complex index refraction of the biological material from the UV to the LWIR. Using that result with particle size distribution and shape information as inputs to T-matrix or discrete dipole approximation (DDA) calculations yields the extinction cross-section and backscatter cross section as a function of wavelength. These are important inputs to the lidar equation. In a continuing effort to provide validated optical cross-sections, measurements have been made on a number of high purity biological species in the laboratory as well as measurements of material released at recent field tests. The resulting observed differences between laboratory and field measurements aid in distinguishing between intrinsic and extrinsic effects, which can affect the characteristic signatures of important biological aerosols. A variety of biological and test aerosols are examined, including Bacillus atrophaeus (BG), and Erwina, ovalbumin, silica and polystyrene.

  7. Evaluation of SAGE II and Balloon-Borne Stratospheric Aerosol Measurements: Evaluation of Aerosol Measurements from SAGE II, HALOE, and Balloonborne Optical Particle Counters

    NASA Technical Reports Server (NTRS)

    Hervig, Mark; Deshler, Terry; Moddrea, G. (Technical Monitor)

    2002-01-01

    Stratospheric aerosol measurements from the University of Wyoming balloonborne optical particle counters (OPCs), the Stratospheric Aerosol and Gas Experiment (SAGE) II, and the Halogen Occultation Experiment (HALOE) were compared in the period 1982-2000, when measurements were available. The OPCs measure aerosol size distributions, and HALOE multiwavelength (2.45-5.26 micrometers) extinction measurements can be used to retrieve aerosol size distributions. Aerosol extinctions at the SAGE II wavelengths (0.386-1.02 micrometers) were computed from these size distributions and compared to SAGE II measurements. In addition, surface areas derived from all three experiments were compared. While the overall impression from these results is encouraging, the agreement can change with latitude, altitude, time, and parameter. In the broadest sense, these comparisons fall into two categories: high aerosol loading (volcanic periods) and low aerosol loading (background periods and altitudes above 25 km). When the aerosol amount was low, SAGE II and HALOE extinctions were higher than the OPC estimates, while the SAGE II surface areas were lower than HALOE and the OPCS. Under high loading conditions all three instruments mutually agree to within 50%.

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

    NASA Technical Reports Server (NTRS)

    Thorsen, Tyler; Fu, Qiang

    2015-01-01

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

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

    NASA Technical Reports Server (NTRS)

    Thorsen, Tyler; Fu, Qiang

    2016-01-01

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

  10. Analysis of the unresolved organic fraction in atmospheric aerosols with ultrahigh-resolution mass spectrometry and nuclear magnetic resonance spectroscopy: organosulfates as photochemical smog constituents.

    PubMed

    Schmitt-Kopplin, Philippe; Gelencsér, Andras; Dabek-Zlotorzynska, Ewa; Kiss, Gyula; Hertkorn, Norbert; Harir, Mourad; Hong, Yang; Gebefügi, Istvan

    2010-10-01

    Complementary molecular and atomic signatures obtained from Fourier transform ion cyclotron resonance (FTICR) mass spectra and NMR spectra provided unequivocal attribution of CHO, CHNO, CHOS, and CHNOS molecular series in secondary organic aerosols (SOA) and high-resolution definition of carbon chemical environments. Sulfate esters were confirmed as major players in SOA formation and as major constituents of its water-soluble fraction (WSOC). Elevated concentrations of SO(2), sulfate, and photochemical activity were shown to increase the proportion of SOA sulfur-containing compounds. Sulfonation of CHO precursors by means of heterogeneous reactions between carbonyl derivatives and sulfuric acid in gas-phase photoreactions was proposed as a likely formation mechanism of CHOS molecules. In addition, photochemistry induced oligomerization processes of CHOS molecules. Methylesters found in methanolic extracts of a SOA subjected to strong photochemical exposure were considered secondary products derived from sulfate esters by methanolysis. The relative abundance of nitrogen-containing compounds (CHNO and CHNOS series) appeared rather dependent on local effects such as biomass burning. Extensive aliphatic branching and disruption of extended NMR spin-systems by carbonyl derivatives and other heteroatoms were the most significant structural motifs in SOA. The presence of heteroatoms in elevated oxidation states suggests a clearly different SOA formation trajectory in comparison with established terrestrial and aqueous natural organic matter.

  11. [Two Data Inversion Algorithms of Aerosol Horizontal Distributiol Detected by MPL and Error Analysis].

    PubMed

    Lü, Li-hui; Liu, Wen-qing; Zhang, Tian-shu; Lu, Yi-huai; Dong, Yun-sheng; Chen, Zhen-yi; Fan, Guang-qiang; Qi, Shao-shuai

    2015-07-01

    Atmospheric aerosols have important impacts on human health, the environment and the climate system. Micro Pulse Lidar (MPL) is a new effective tool for detecting atmosphere aerosol horizontal distribution. And the extinction coefficient inversion and error analysis are important aspects of data processing. In order to detect the horizontal distribution of atmospheric aerosol near the ground, slope and Fernald algorithms were both used to invert horizontal MPL data and then the results were compared. The error analysis showed that the error of the slope algorithm and Fernald algorithm were mainly from theoretical model and some assumptions respectively. Though there still some problems exist in those two horizontal extinction coefficient inversions, they can present the spatial and temporal distribution of aerosol particles accurately, and the correlations with the forward-scattering visibility sensor are both high with the value of 95%. Furthermore relatively speaking, Fernald algorithm is more suitable for the inversion of horizontal extinction coefficient.

  12. Research in Depolarization and Extinction Coefficient of Particles in Tibetan Plateau by Lidar

    NASA Astrophysics Data System (ADS)

    Dai, Guangyao; Song, Xiaoquan; Zhai, Xiaochun; Wu, Songhua

    2016-06-01

    Vertical profiles of the depolarization ratio and the extinction coefficient of atmospheric particles in Tibetan Plateau were measured with the OUC Water Vapor, Cloud and Aerosol Lidar during the 3rd Tibetan Plateau Atmospheric Expedition Experiment Campaign in 2013 and 2014. The cloud types and phases, the spatial temporal distribution of the aerosols and the boundary layer height in the Tibetan Plateau were obtained using polarization lidar technique. In this paper, the depolarization ratio was validated with CALIOP polarization simultaneous data, and the extinction coefficient was retrieved by the Fernald method. The result implied that the atmosphere in the Tibetan Plateau was quite clean with low aerosol load and serious pollution. The ice-water mixed cumulus, water cumulus or stratus clouds in Litang and Nagqu were occurred and classified, respectively. The boundary layer height in Nagqu at average altitude over 4600 m was obtained at around 200 m-300 m, which was commonly lower than that in other observed sites.

  13. Particulate contribution to extinction of visible radiation: Pollution, haze, and fog

    NASA Astrophysics Data System (ADS)

    Elias, Thierry; Haeffelin, Martial; Drobinski, Philippe; Gomes, Laurent; Rangognio, Jerome; Bergot, Thierry; Chazette, Patrick; Raut, Jean-Christophe; Colomb, Michèle

    2009-06-01

    A data set acquired by eight particle-dedicated instruments set up on the SIRTA (Site Instrumental de Recherche par Télédétection Atmosphérique, which is French for Instrumented Site for Atmospheric Remote Sensing Research) during the ParisFog field campaign are exploited to document microphysical properties of particles contributing to extinction of visible radiation in variable situations. The study focuses on a 48-hour period when atmospheric conditions are highly variable: relative humidity changes between 50 and 100%, visibility ranges between 65 and 35 000 m, the site is either downwind the Paris area either under maritime influence. A dense and homogeneous fog formed during the night by radiative cooling. In 6 h, visibility decreased down from 30 000 m in the clear-sky regime to 65 m within the fog, because of advected urban pollution (factor 3 to 4 in visibility reduction), aerosol hydration (factor 20) and aerosol activation (factor 6). Computations of aerosol optical properties, based on Mie theory, show that extinction in clear-sky regime is due equally to the ultrafine modes and to the accumulation mode. Extinction by haze is due to hydrated aerosol particles distributed in the accumulation mode, defined by a geometric mean diameter of 0.6 μm and a geometric standard deviation of 1.4. These hydrated aerosol particles still contribute by 20 ± 10% to extinction in the fog. The complementary extinction is due to fog droplets distributed around the geometric mean diameter of 3.2 μm with a geometric standard deviation of 1.5 during the first fog development stage. The study also shows that the experimental set-up could not count all fog droplets during the second and third fog development stages.

  14. Investigation of multiple scattering effects in aerosols

    NASA Technical Reports Server (NTRS)

    Deepak, A.

    1980-01-01

    The results are presented of investigations on the various aspects of multiple scattering effects on visible and infrared laser beams transversing dense fog oil aerosols contained in a chamber (4' x 4' x 9'). The report briefly describes: (1) the experimental details and measurements; (2) analytical representation of the aerosol size distribution data by two analytical models (the regularized power law distribution and the inverse modified gamma distribution); (3) retrieval of aerosol size distributions from multispectral optical depth measurements by two methods (the two and three parameter fast table search methods and the nonlinear least squares method); (4) modeling of the effects of aerosol microphysical (coagulation and evaporation) and dynamical processes (gravitational settling) on the temporal behavior of aerosol size distribution, and hence on the extinction of four laser beams with wavelengths 0.44, 0.6328, 1.15, and 3.39 micrometers; and (5) the exact and approximate formulations for four methods for computing the effects of multiple scattering on the transmittance of laser beams in dense aerosols, all of which are based on the solution of the radiative transfer equation under the small angle approximation.

  15. Aerosol measurements from earth orbiting spacecraft

    NASA Technical Reports Server (NTRS)

    Mccormick, M. P.

    1982-01-01

    The global aerosol data base evolving from monitoring being done by Stratospheric Aerosol Measurement (SAM) II and Stratospheric Aerosol and Gas Experiment (SAGE) since the fall of 1978 is presented. Data reveal that polar stratospheric clouds (PSC) enhance extinction and optical depths by up to two orders of magnitude and an order of magnitude, respectively. These data are over background 1000 nm values of approximately 1.2 x 10 to the -4th per km, and 1.3 x 10 to the -3rd, respectively. SAGE has offered, for the first time, quantitative measurements of volcanic eruptions on a nearly global basis, and estimates are given for the amount of aerosol injected into the stratosphere from each volcano. For example, Northern Hemisphere aerosol was enhanced by more than 100% by the 1980 eruption of Mount St. Helens, which produced about 0.32 x 10 to the 6th metric tons of aerosol. A cirrus cloud data base is being developed which will be useful in earth radiation and water vapor budget studies. Cross-section, contour, and temperature variation diagrams are included.

  16. Optimal Aerosol Parameterization for Remote Sensing Retrievals

    NASA Technical Reports Server (NTRS)

    Newchurch, Michael J.

    2004-01-01

    We have developed a new algorithm for the retrieval of aerosol and gases from SAGE It1 solar transmission measurements. This algorithm improves upon the NASA operational algorithm in several key aspects, including solving the problem non-linearly and incorporating a new methodology for separating the contribution of aerosols and gases. In order to extract aerosol information we have built a huge database of aerosol models for both stratospheric and tropospheric aerosols, and polar stratospheric cloud particles. This set of models allows us to calculate a vast range of possible extinction spectra for aerosols. and from these, derive a set of eigenvectors which then provide the basis set used in our inversion algorithm. Our aerosol algorithm and retrievals are described in several articles (listed in References Section) published under this grant. In particular they allow us to analyze the spectral properties of aerosols and PSCs and ultimately derive their microphysical properties. We have found some considerable differences between our spectra and the ones derived from the SAGE III operational algorithm. These are interesting as they provide an independent check on the validity of published aerosol data and, in particular, on their associated uncertainties. In order to understand these differences, we are assembling independent aerosol data from other sources with which to make comparisons. We have carried out extensive comparisons of our ozone retrievals with both SAGE III and independent lidar, ozonesonde, and satellite measurements (Polyakov et al., 2004). These show very good agreement throughout the stratosphere and help to quantify differences which can be attributed to natural variation in ozone versus that produced by algorithmic differences. In the mid - upper stratosphere, agreement with independent data was generally within 5 - 20%. but in the lower stratosphere the differences were considerably larger. We believe that a large proportion of this

  17. Interstellar Extinction and its Variation in the Galaxy

    NASA Astrophysics Data System (ADS)

    Ford Schlafly, Edward; Rix, Hans-Walter; Finkbeiner, Douglas P.; Green, Gregory; Lee, Albert; Meisner, Aaron M.

    2016-01-01

    Dust reddening is an important diagnostic of the interstellar medium and the dust grain size distribution, as well as a pervasive observational nuisance. Detailed studies of the dust extinction curve and its variation have hithertofore been largely limited to samples of hundreds of specially chosen stars. We use spectroscopy from APOGEE in combination with photometry from Pan-STARRS1, 2MASS, and WISE to characterize the dust extinction curve throughout much of the nearest few kiloparsecs of the Galactic plane using tens of thousands of stars. We make new measurements of the dust extinction curve and its variation, finding that the extinction curve in the optical through infrared is well characterized by a one-parameter family of curves, described, for instance, by R(V). Our data show little evidence of any need for further parameters. The local curvature of the extinction curve increases with decreasing R(V) throughout most of the optical and infrared: the extinction curve in the infrared is not more ``universal'' than in the optical, in contrast to several widely-used extinction curve parameterizations. We find that the shape of the dust extinction curve is rather uniform, with σ(R(V)) = 0.2, and with less than two percent of sight lines having R(V) > 4. However, significant spatially coherent variations in R(V) do exist. The primary variations are on scales much larger than individual molecular clouds, indicating that grain growth in dense molecular cloud environments is not the primary driver of R(V) variations in dust at large. Indeed, we find no correlation between R(V) and dust column density out to E(B-V) ≈ 2.

  18. Aerosol measurements at the south pole during 1987. Data report

    SciTech Connect

    Bodhaine, B.A.; Harris, J.M.

    1992-11-01

    The Climate Monitoring and Diagnostics Laboratory (CMDL) of the National Oceanic and Atmospheric Administration (NOAA) operates an atmospheric monitoring observatory at Amundsen-Scott Station, South Pole. The aerosol measurement program consists of the continuous measurement of condensation nuclei (CN) concentration and aerosol scattering extinction coefficient. During 1987, a special aerosol experiment was conducted that included filter samples for subsequent analysis by the proton induced x-ray emission technique, diffusion battery measurements for size information in the sub-0.1 micrometer size range, and aerosol absorption measurements using an aethalometer. Surface and upper air meteorological data were also available. The purpose of the report is to present all of the aerosol data obtained during 1987.

  19. Originations and Extinctions

    NASA Astrophysics Data System (ADS)

    Ray, Tane; Moseley, Leo; Jan, Naeem

    We analyse the fossil data of Benton1 with and without interpolation schemes. By Fourier transform analysis, we find a frequency dependence of the amplitude of 1/f for the various interpolation schemes used in the past. We illustrate that shuffling the interpolated data changes the spectra only slightly. On the other hand, an identical analysis performed on the raw (uninterpolated) fossil data gives a flat frequency spectrum. We conclude that the 1/f behavior is an artifact of the interpolation schemes. We next introduce a simulation of extinctions driven only by interactions between two trophic levels. Fourier transform analysis of the simulation data shows a frequency dependence of 1/f. When the data are grouped into a form resembling the fossil record the frequency dependence vanishes, giving a flat spectrum. Our simulation produces a frequency spectrum that agrees with the observed fossil record.

  20. Acoustic integrated extinction

    PubMed Central

    Norris, Andrew N.

    2015-01-01

    The integrated extinction (IE) is defined as the integral of the scattering cross section as a function of wavelength. Sohl et al. (2007 J. Acoust. Soc. Am. 122, 3206–3210. (doi:10.1121/1.2801546)) derived an IE expression for acoustic scattering that is causal, i.e. the scattered wavefront in the forward direction arrives later than the incident plane wave in the background medium. The IE formula was based on electromagnetic results, for which scattering is causal by default. Here, we derive a formula for the acoustic IE that is valid for causal and non-causal scattering. The general result is expressed as an integral of the time-dependent forward scattering function. The IE reduces to a finite integral for scatterers with zero long-wavelength monopole and dipole amplitudes. Implications for acoustic cloaking are discussed and a new metric is proposed for broadband acoustic transparency. PMID:27547100

  1. An Analysis of AERONET Aerosol Absorption Properties and Classifications Representative of Aerosol Source Regions

    NASA Technical Reports Server (NTRS)

    Giles, David M.; Holben, Brent N.; Eck, Thomas F.; Sinyuk, Aliaksandr; Smirnov, Alexander; Slutsker, Ilya; Dickerson, R. R.; Thompson, A. M.; Schafer, J. S.

    2012-01-01

    Partitioning of mineral dust, pollution, smoke, and mixtures using remote sensing techniques can help improve accuracy of satellite retrievals and assessments of the aerosol radiative impact on climate. Spectral aerosol optical depth (tau) and single scattering albedo (omega (sub 0) ) from Aerosol Robotic Network (AERONET) measurements are used to form absorption [i.e., omega (sub 0) and absorption Angstrom exponent (alpha(sub abs))] and size [i.e., extinction Angstrom exponent (alpha(sub ext)) and fine mode fraction of tau] relationships to infer dominant aerosol types. Using the long-term AERONET data set (1999-2010), 19 sites are grouped by aerosol type based on known source regions to: (1) determine the average omega (sub 0) and alpha(sub abs) at each site (expanding upon previous work); (2) perform a sensitivity study on alpha(sub abs) by varying the spectral omega (sub 0); and (3) test the ability of each absorption and size relationship to distinguish aerosol types. The spectral omega (sub 0) averages indicate slightly more aerosol absorption (i.e., a 0.0 < delta omega (sub 0) <= 0.02 decrease) than in previous work and optical mixtures of pollution and smoke with dust show stronger absorption than dust alone. Frequency distributions of alpha(sub abs) show significant overlap among aerosol type categories and at least 10% of the alpha(sub abs) retrievals in each category are below 1.0. Perturbing the spectral omega (sub 0) by +/- 0.03 induces significant alpha(sub abs) changes from the unperturbed value by at least approx. +/- 0.6 for Dust, approx. +/-0.2 for Mixed, and approx. +/-0.1 for Urban/Industrial and Biomass Burning. The omega (sub 0)440nm and alpha(sub ext) 440-870nm relationship shows the best separation among aerosol type clusters, providing a simple technique for determining aerosol type from surface- and future space-based instrumentation.

  2. Influences of relative humidity on aerosol optical properties and aerosol radiative forcing during ACE-Asia

    NASA Astrophysics Data System (ADS)

    Yoon, Soon-Chang; Kim, Jiyoung

    In situ measurements at Gosan, South Korea, and onboard C-130 aircraft during ACE-Asia were analyzed to investigate the influence of relative humidity (RH) on aerosol optical properties and radiative forcing. The temporal variation of aerosol chemical composition at the Gosan super-site was highly dependent on the air mass transport pathways and source region. RH in the springtime over East Asia were distributed with very high spatial and temporal variation. The RH profile onboard C-130 aircraft measurements exhibits a mixed layer height of about 2 km. Aerosol scattering coefficient ( σsp) under ambient RH was greatly enhanced as compared with that at dry RH (RH<40%). From the aerosol optical and radiative transfer modeling studies, we found that the extinction and scattering coefficients are greatly enhanced with RH. Single scattering albedo with RH is also sensitively changed in the longer wavelength. Asymmetry parameter ( g) is gradually increased with RH although g decreases with wavelength at a given RH. Aerosol optical depth (AOD) at 550 nm and RH of 50% increased to factors 1.24, 1.51, 2.16, and 3.20 at different RH levels 70, 80, 90, and 95%, respectively. Diurnal-averaged aerosol radiative forcings for surface, TOA, and atmosphere were increased with RH because AOD was increased with RH due to hygroscopic growth of aerosol particles. This result implies that the hygroscopic growth due to water-soluble or hydrophilic particles in the lower troposphere may significantly modify the magnitude of aerosol radiative forcing both at the surface and TOA. However, the diurnal-averaged radiative forcing efficiencies at the surface, TOA, and atmosphere were decreased with increasing RH. The decrease of the forcing efficiency with RH results from the fact that increasing rate of aerosol optical depth with RH is greater than the increasing rate of aerosol radiative forcing with RH.

  3. Pinpointing and preventing imminent extinctions.

    PubMed

    Ricketts, Taylor H; Dinerstein, Eric; Boucher, Tim; Brooks, Thomas M; Butchart, Stuart H M; Hoffmann, Michael; Lamoreux, John F; Morrison, John; Parr, Mike; Pilgrim, John D; Rodrigues, Ana S L; Sechrest, Wes; Wallace, George E; Berlin, Ken; Bielby, Jon; Burgess, Neil D; Church, Don R; Cox, Neil; Knox, David; Loucks, Colby; Luck, Gary W; Master, Lawrence L; Moore, Robin; Naidoo, Robin; Ridgely, Robert; Schatz, George E; Shire, Gavin; Strand, Holly; Wettengel, Wes; Wikramanayake, Eric

    2005-12-20

    Slowing rates of global biodiversity loss requires preventing species extinctions. Here we pinpoint centers of imminent extinction, where highly threatened species are confined to single sites. Within five globally assessed taxa (i.e., mammals, birds, selected reptiles, amphibians, and conifers), we find 794 such species, three times the number recorded as having gone extinct since 1500. These species occur in 595 sites, concentrated in tropical forests, on islands, and in mountainous areas. Their taxonomic and geographical distribution differs significantly from that of historical extinctions, indicating an expansion of the current extinction episode beyond sensitive species and places toward the planet's most biodiverse mainland regions. Only one-third of the sites are legally protected, and most are surrounded by intense human development. These sites represent clear opportunities for urgent conservation action to prevent species loss.

  4. Extinction of Harrington's mountain goat

    PubMed Central

    Mead, Jim I.; Martin, Paul S.; Euler, Robert C.; Long, Austin; Jull, A. J. T.; Toolin, Laurence J.; Donahue, Douglas J.; Linick, T. W.

    1986-01-01

    Keratinous horn sheaths of the extinct Harrington's mountain goat, Oreamnos harringtoni, were recovered at or near the surface of dry caves of the Grand Canyon, Arizona. Twenty-three separate specimens from two caves were dated nondestructively by the tandem accelerator mass spectrometer (TAMS). Both the TAMS and the conventional dates indicate that Harrington's mountain goat occupied the Grand Canyon for at least 19,000 years prior to becoming extinct by 11,160 ± 125 radiocarbon years before present. The youngest average radiocarbon dates on Shasta ground sloths, Nothrotheriops shastensis, from the region are not significantly younger than those on extinct mountain goats. Rather than sequential extinction with Harrington's mountain goat disappearing from the Grand Canyon before the ground sloths, as one might predict in view of evidence of climatic warming at the time, the losses were concurrent. Both extinctions coincide with the regional arrival of Clovis hunters. Images PMID:16593655

  5. Interstellar extinction in the ultraviolet

    NASA Technical Reports Server (NTRS)

    Bless, R. C.; Savage, B. D.

    1972-01-01

    Interstellar extinction curves over the region 3600-1100 A for 17 stars are presented. The observations were made by the two Wisconsin spectrometers onboard the OAO-2 with spectral resolutions of 10 A and 20 A. The extinction curves generally show a pronounced maximum at 2175 plus or minus 25 A, a broad minimum in the region 1800-1350 A, and finally a rapid rise to the far ultraviolet. Large extinction variations from star to star are found, especially in the far ultraviolet; however, with only two possible exceptions in this sample, the wavelength at the maximum of the extinction bump is essentially constant. These data are combined with visual and infrared observations to display the extinction behavior over a range in wavelength of about a factor of 20.

  6. Extinction of Harrington's Mountain Goat

    NASA Astrophysics Data System (ADS)

    Mead, Jim I.; Martin, Paul S.; Euler, Robert C.; Long, Austin; Jull, A. J. T.; Toolin, Laurence J.; Donahue, Douglas J.; Linick, T. W.

    1986-02-01

    Keratinous horn sheaths of the extinct Harrington's mountain goat, Oreamnos harringtoni, were recovered at or near the surface of dry caves of the Grand Canyon, Arizona. Twenty-three separate specimens from two caves were dated nondestructively by the tandem accelerator mass spectrometer (TAMS). Both the TAMS and the conventional dates indicate that Harrington's mountain goat occupied the Grand Canyon for at least 19,000 years prior to becoming extinct by 11,160 ± 125 radiocarbon years before present. The youngest average radiocarbon dates on Shasta ground sloths, Nothrotheriops shastensis, from the region are not significantly younger than those on extinct mountain goats. Rather than sequential extinction with Harrington's mountain goat disappearing from the Grand Canyon before the ground sloths, as one might predict in view of evidence of climatic warming at the time, the losses were concurrent. Both extinctions coincide with the regional arrival of Clovis hunters.

  7. Extinction of Harrington's mountain goat

    SciTech Connect

    Mead, J.I.; Martin, P.S.; Euler, R.C.; Long, A.; Jull, A.J.T.; Toolin, L.J.; Donahue, D.J.; Linick, T.W.

    1986-02-01

    Keratinous horn sheaths of the extinct Harrington's mountain goat, Oreamnos harringtoni, were recovered at or near the surface of dry caves of the Grand Canyon, Arizona. Twenty-three separate specimens from two caves were dated nondestructively by the tandem accelerator mass spectrometer (TAMS). Both the TAMS and the conventional dates indicate that Harrington's mountain goat occupied the Grand Canyon for at least 19,000 years prior to becoming extinct by 11,160 +/- 125 radiocarbon years before present. The youngest average radiocarbon dates on Shasta ground sloths, Nothrotheriops shastensis, from the region are not significantly younger than those on extinct mountain goats. Rather than sequential extinction with Harrington's mountain goat disappearing from the Grand Canyon before the ground sloths, as one might predict in view of evidence of climatic warming at the time, the losses were concurrent. Both extinctions coincide with the regional arrival of Clovis hunters.

  8. Measuring Extinction with ALE

    NASA Astrophysics Data System (ADS)

    Zimmer, Peter C.; McGraw, J. T.; Gimmestad, G. G.; Roberts, D.; Stewart, J.; Smith, J.; Fitch, J.

    2007-12-01

    ALE (Astronomical LIDAR for Extinction) is deployed at the University of New Mexico's (UNM) Campus Observatory in Albuquerque, NM. It has begun a year-long testing phase prior deployment at McDonald Observatory in support of the CCD/Transit Instrument II (CTI-II). ALE is designed to produce a high-precision measurement of atmospheric absorption and scattering above the observatory site every ten minutes of every moderately clear night. LIDAR (LIght Detection And Ranging) is the VIS/UV/IR analog of radar, using a laser, telescope and time-gated photodetector instead of a radio transmitter, dish and receiver. In the case of ALE -- an elastic backscatter LIDAR -- 20ns-long, eye-safe laser pulses are launched 2500 times per second from a 0.32m transmitting telescope co-mounted with a 50mm short-range receiver on an alt-az mounted 0.67m long-range receiver. Photons from the laser pulse are scattered and absorbed as the pulse propagates through the atmosphere, a portion of which are scattered into the field of view of the short- and long-range receiver telescopes and detected by a photomultiplier. The properties of a given volume of atmosphere along the LIDAR path are inferred from both the altitude-resolved backscatter signal as well as the attenuation of backscatter signal from altitudes above it. We present ALE profiles from the commissioning phase and demonstrate some of the astronomically interesting atmospheric information that can be gleaned from these data, including, but not limited to, total line-of-sight extinction. This project is funded by NSF Grant 0421087.

  9. ENCAPSULATED AEROSOLS

    DTIC Science & Technology

    materials determine the range of applicability of each method. A useful microencapsulation method, based on coagulation by inertial force was developed...The generation apparatus, consisting of two aerosol generators in series, was utilized to produce many kinds of microcapsules . A fluid energy mill...was found useful for the production of some microcapsules . The permeability of microcapsule films and the effect of exposure time and humidity were

  10. The end-Permian mass extinction: A complex, multicausal extinction

    NASA Technical Reports Server (NTRS)

    Erwin, D. H.

    1994-01-01

    The end-Permian mass extinction was the most extensive in the history of life and remains one of the most complex. Understanding its causes is particularly important because it anchors the putative 26-m.y. pattern of periodic extinction. However, there is no good evidence for an impact and this extinction appears to be more complex than others, involving at least three phases. The first began with the onset of a marine regression during the Late Permian and resulting elimination of most marine basins, reduction in habitat area, and increased climatic instability; the first pulse of tetrapod extinctions occurred in South Africa at this time. The second phase involved increased regression in many areas (although apparently not in South China) and heightened climatic instability and environmental degradation. Release of gas hydrates, oxidation of marine carbon, and the eruption of the Siberian flood basalts occurred during this phase. The final phase of the extinction episode began with the earliest Triassic marine regression and destruction of nearshore continental habitats. Some evidence suggests oceanic anoxia may have developed during the final phase of the extinction, although it appears to have been insufficient to the sole cause of the extinction.

  11. Aerosol properties derived from spectral actinic flux measurements

    NASA Astrophysics Data System (ADS)

    Stark, H.; Schmidt, K. S.; Pilewskie, P.; Cozic, J.; Wollny, A. G.; Brock, C. A.; Baynard, T.; Lack, D.; Parrish, D. D.; Fehsenfeld, F. C.

    2008-12-01

    Measurement of aerosol properties is very important for understanding climate change. Aerosol optical properties influence solar radiation throughout the troposphere. According to the Working Group I report of the intergovernmental panel for climate change [IPCC, 2007], aerosols have a direct radiative forcing of - 0.5±0.4 W/m2 with a medium to low level of scientific understanding. This relatively large uncertainty indicates the need for more frequent and precise measurements of aerosol properties. We will show how actinic flux measurements can be used to derive important optical aerosol parameters such as aerosol optical thickness and depth, surface albedo, angstrom exponent, radiative forcing by clouds and aerosols, aerosol extinction, and others. The instrument used for this study is a combination of two spectroradiometers measuring actinic flux in the ultraviolet and visible radiation range from 280 to 690 nm with a resolution of 1 nm. Actinic flux is measured as the radiation incident on a spherical surface with sensitivity independent of direction. In contrast, irradiance is measured as the radiation incident on a plane surface, which depends on the cosine of the incident angle. Our goal is to assess the capabilities of using spectral actinic flux measurements to derive various aerosol properties. Here we will compare 1) actinic flux measurements to irradiance measurements from the spectral solar flux radiometer (SSFR), 2) derived aerosol size distributions with measurements from a white light optical particle counter (WLOPC) and ultra high sensitivity aerosol size spectrometer (UHSAS), and 3) derived aerosol optical extinction with measurements from a cavity ringdown aerosol extinction spectrometer (CRD-AES). These comparisons will utilize data from three recent field campaigns over New England and the Atlantic Ocean (ICARTT 2004), Texas and the Gulf of Mexico during (TexAQS/GoMACCS 2006), and Alaska and the Arctic Ocean (ARCPAC 2008) when the instruments

  12. Aerosol Correction for Improving OMPS/LP Ozone Retrieval

    NASA Technical Reports Server (NTRS)

    Chen, Zhong; Bhartia, Pawan K.; Loughman, Robert

    2015-01-01

    The Ozone Mapping and Profiler Suite Limb Profiler (OMPS-LP) on board the Suomi National Polar-orbiting Partnership (SNPP) satellite was launched on Oct. 28, 2011. Limb profilers measures the radiance scattered from the Earth's atmospheric in limb viewing mode from 290 to 1000 nm and infer ozone profiles from tropopause to 60 km. The recently released OMPS-LP Version 2 data product contains the first publicly released ozone profiles retrievals, and these are now available for the entire OMPS mission, which extends from April, 2012. The Version 2 data product retrievals incorporate several important improvements to the algorithm. One of the primary changes is to turn off the aerosol retrieval module. The aerosol profiles retrieved inside the ozone code was not helping the ozone retrieval and was adding noise and other artifacts. Aerosols including polar stratospheric cloud (PSC) and polar mesospheric clouds (PMC) have a detectable effect on OMPS-LP data. Our results show that ignoring the aerosol contribution would produce an ozone density bias of up to 10 percent in the region of maximum aerosol extinction. Therefore, aerosol correction is needed to improve the quality of the retrieved ozone concentration profile. We provide Aerosol Scattering Index (ASI) for detecting aerosols-PMC-PSC, defined as ln(Im-Ic) normalized at 45km, where Im is the measured radiance and Ic is the calculated radiance assuming no aerosols. Since ASI varies with wavelengths, latitude and altitude, we can start by assuming no aerosol profiles in calculating the ASIs and then use the aerosol profile to see if it significantly reduces the residuals. We also discuss the effect of aerosol size distribution on the ozone profile retrieval process. Finally, we present an aerosol-PMC-PSC correction scheme.

  13. Aerosol Optical Properties Measured Onboard the Ronald H. Brown During ACE Asia as a Function of Aerosol Chemical Composition and Source Region

    NASA Technical Reports Server (NTRS)

    Quinn, P. K.; Coffman, D. J.; Bates, T. S.; Welton, E. J.; Covert, D. S.; Miller, T. L.; Johnson, J. E.; Maria, S.; Russell, L.; Arimoto, R.

    2004-01-01

    During the ACE Asia intensive field campaign conducted in the spring of 2001 aerosol properties were measured onboard the R/V Ronald H. Brown to study the effects of the Asian aerosol on atmospheric chemistry and climate in downwind regions. Aerosol properties measured in the marine boundary layer included chemical composition; number size distribution; and light scattering, hemispheric backscattering, and absorption coefficients. In addition, optical depth and vertical profiles of aerosol 180 deg backscatter were measured. Aerosol within the ACE Asia study region was found to be a complex mixture resulting from marine, pollution, volcanic, and dust sources. Presented here as a function of air mass source region are the mass fractions of the dominant aerosol chemical components, the fraction of the scattering measured at the surface due to each component, mass scattering efficiencies of the individual components, aerosol scattering and absorption coefficients, single scattering albedo, Angstrom exponents, optical depth, and vertical profiles of aerosol extinction. All results except aerosol optical depth and the vertical profiles of aerosol extinction are reported at a relative humidity of 55 +/- 5%. An over-determined data set was collected so that measured and calculated aerosol properties could be compared, internal consistency in the data set could be assessed, and sources of uncertainty could be identified. By taking into account non-sphericity of the dust aerosol, calculated and measured aerosol mass and scattering coefficients agreed within overall experimental uncertainties. Differences between measured and calculated aerosol absorption coefficients were not within reasonable uncertainty limits, however, and may indicate the inability of Mie theory and the assumption of internally mixed homogeneous spheres to predict absorption by the ACE Asia aerosol. Mass scattering efficiencies of non-sea salt sulfate aerosol, sea salt, submicron particulate organic

  14. Longwave radiative forcing by aqueous aerosols

    SciTech Connect

    Gaffney, J.S.; Marley, N.A.

    1995-01-01

    Recently, a great deal of interest has been focused on the role of aerosols in climatic change because of their potential cooling impacts due to light scattering. Recent advances in infrared spectroscopy using cylindrical internal reflectance have allowed the longwave absorption of dissolved aerosol species and the associated liquid water to be accurately determined and evaluated. Experimental measurements using these techniques have shown that dissolved sulfate, nitrate, and numerous other aerosol species will act to cause greenhouse effects. Preliminary calculations indicate that the longwave climate forcing (i.e., heating) for sulfate aerosol will be comparable in magnitude to the cooling effect produced by light scattering. However, more detailed modeling will clearly be needed to address the impact of the longwave forcing due to aerosols as a function of atmospheric height and composition. Their work has shown that aerosol composition will be important in determining longwave forcing, while shortwave forcing will be more related to the physical size of the aerosol droplets. On the basis of these studies, it is increasingly apparent that aerosols, fogs, and clouds play a key role in determining the radiative balance of the atmosphere and in controlling regional and global climates.

  15. At-Sea Evaluation of the Obscuration Characteristics of a Hygroscopic Aerosol Smoke Produced by the CY85A Pyrotechnic

    DTIC Science & Technology

    1983-12-01

    and IiWIU* by block nmber) Salty Dog Obscuration .2Hygroscopic aerosol Extinction ISmoke Pyrotechnically Generated ’For the past six years, Calapan, in...Extinction Characteristics for Salty Dog , NWC 29 and NWC 78 Pyrotechnics,", Calspan Report No. 6663-M-l, 40 pp, Calspan Corporation, Buffalo, NY 14225. 4

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

    NASA Astrophysics Data System (ADS)

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

    2013-08-01

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

  17. Absorption characteristics of aerosols over the northwestern region of India: Distinct seasonal signatures of biomass burning aerosols and mineral dust

    NASA Astrophysics Data System (ADS)

    Gogoi, Mukunda M.; Suresh Babu, S.; Krishna Moorthy, K.; Manoj, M. R.; Chaubey, Jai Prakash

    2013-07-01

    Continuous measurements of aerosol black carbon (BC) mass concentrations made over a period of 3 years from a semi-arid, near-coastal, remote and sparsely inhabited location along with satellite-based data of aerosol absorption index, optical depth and extinction profiles in western India are used to characterize the distinct nature of aerosols near the surface and in the free troposphere and their seasonality. Despite being far remote and sparsely inhabited, significant levels of BC are observed in the ambient during winter (1.45 ± 0.71 μg m-3) attributed to biomass burning aerosols, advected to the site from the north and west; while during summer the concentrations are far reduced (0.23 ± 0.11 μg m-3) and represent the apparent background concentrations. The spectral absorption coefficients suggest the BC during summer be mostly of fossil fuel combustions. The strong convective boundary layer dynamics produces significant diurnal variation during winter and modulates to a lesser extent the seasonal variation. Examination of aerosol (absorption) index from OMI data for the study period showed a seasonal pattern that is almost opposite to that seen at the surface; with high aerosol index in summer, showing a significant difference between the surface and columnar aerosol types in summer. MISR and MODIS-derived columnar AOD follow the OMI pattern. Analysis of the vertical profiles of aerosol extinction and volume depolarization ratio (VDR), derived from CALIPSO data indicates the presence of strong dust layers with VDR ˜ 0.3 in the altitude region 4-6 km, contributing to the high aerosol index in the OMI data, while the surface measurements show absorptive properties representing fossil fuel BC aerosols.

  18. Sensitivity of aerosol retrieval over snow surfaces

    NASA Astrophysics Data System (ADS)

    Seidel, F. C.; Painter, T. H.

    2011-12-01

    Significant amounts of black carbon and dust aerosols are transported to and accumulated in snowpacks of mountain ranges around the globe. The direct climate forcing of these particles is increasingly understood, whereas its indirect radiative forcing due to snow albedo and snow cover changes is still under investigation. In-situ and new remote sensing techniques are used to estimate snowpack properties from local to regional scales. Nevertheless, orbital and suborbital Earth observation data are difficult to analyze due to high spatial variability of the snowpack in rugged terrain. In addition, changes in atmospheric turbidity significantly complicate the estimation of snow cover characteristics and requires prior retrieval of optical and microphysical aerosol properties. Unfortunately, most aerosol retrieval techniques work only over dark surfaces. We therefore present a study on the sensitivity of aerosol optical depth (AOD) retrieval over snow surfaces. Radiative transfer calculations show that the sensitivity to surface spectral albedo depends strongly on the aerosol single scattering albedo (ratio of scattering efficiency to total extinction efficiency). Absorbing aerosol types (e.g. soot) provide a relatively good AOD retrieval sensitivity for very bright surfaces. The findings provide a basis for the development of future techniques and algorithms, which are able to concurrently retrieve snow and aerosol properties using remote sensing data. We explore these sensitivities with synthetic data and a time series of imaging spectrometer data, in situ spectral irradiance measurements, and sunphotometer measurements of AOD in the mountains of the Upper Colorado River Basin, USA. Ultimately, this research is important to map and better understand regional influences of aerosol and climate forcings on the cryosphere and water cycle in mountainous and other cold regions.

  19. Infrared and X-ray Absorption Near Edge Structure Spectroscopy Analyses of the Titan Haze Simulation (THS) Aerosols Produced at Low Temperature (200 K)

    NASA Astrophysics Data System (ADS)

    Sciamma-O'Brien, Ella; Salama, Farid

    2016-10-01

    We present our latest results on the Titan Haze Simulation (THS) experiment developed on the COSmIC simulation chamber at NASA Ames. In Titan's atmosphere, a complex organic chemistry induced by UV radiation and electron bombardment occurs between N2 and CH4 and leads to the production of larger molecules and solid aerosols. In the THS, Titan's chemistry is simulated by pulsed plasma in the stream of a supersonic expansion, at Titan-like temperature (200 K). The residence time of the gas in the pulsed plasma discharge is ~3 µs, hence the chemistry is truncated allowing us to probe the first and intermediate steps of the chemistry, by adding heavier precursors into the initial N2-CH4 gas mixture. Experiments have been performed in different gas mixtures from the simpler N2-CH4 (98:2 and 95:5), to more complex mixtures: N2-CH4-C2H2 (91:5:4 and 94.5:5:0.5), N2-CH4-C6H6 (90:5:5) and N2-CH4-C2H2-C6H6 (86:5:4:5). Both the gas and solid phases have been analyzed using a combination of in situ and ex situ diagnostics.A recent mass spectrometry analysis of the gas phase demonstrated that the THS is a unique tool to monitor the different steps of the N2-CH4 chemistry [1]. The results of the solid phase study are consistent with the chemical growth evolution observed in the gas phase. The solid phase products are in the form of grains produced in volume and not from interaction on the substrate's surface. Scanning Electron Microscopy images have shown that more complex mixtures produce larger aggregates (100-500 nm in N2-CH4, up to 5 µm in N2-CH4-C2H2-C6H6). Moreover, the morphology of the grains seems to depend on the precursors, a finding that could have an impact on Titan haze microphysical models. We will present the latest results of the infrared and x-ray absorption near edge structure spectroscopic measurements that have been performed on all four mixtures. These results provide information on the nature of the different functional groups present in our samples as

  20. Short-term Variability of Extinction by Broadband Stellar Photometry

    SciTech Connect

    Musat, I.C.; Ellingson, R.G.

    2005-03-18

    Aerosol optical depth variation over short-term time intervals is determined from broadband observations of stars with a whole sky imager. The main difficulty in such measurements consists of accurately separating the star flux value from the non-stellar diffuse skylight. Using correction method to overcome this difficulty, the monochromatic extinction at the ground due to aerosols is extracted from heterochromatic measurements. A form of closure is achieved by comparison with simultaneous or temporally close measurements with other instruments, and the total error of the method, as a combination of random error of measurements and systematic error of calibration and model, is assessed as being between 2.6 and 3% rms.

  1. Plant invasions and extinction debts.

    PubMed

    Gilbert, Benjamin; Levine, Jonathan M

    2013-01-29

    Whether introduced species invasions pose a major threat to biodiversity is hotly debated. Much of this debate is fueled by recent findings that competition from introduced organisms has driven remarkably few plant species to extinction. Instead, native plant species in invaded ecosystems are often found in refugia: patchy, marginal habitats unsuitable to their nonnative competitors. However, whether the colonization and extinction dynamics of these refugia allow long-term native persistence is uncertain. Of particular concern is the possibility that invasive plants may induce an extinction debt in the native flora, where persistence over the short term masks deterministic extinction trajectories. We examined how invader impacts on landscape structure influence native plant persistence by combining recently developed quantitative techniques for evaluating metapopulation persistence with field measurements of an invaded plant community. We found that European grass invasion of an edaphically heterogeneous California landscape has greatly decreased the likelihood of the persistence of native metapopulations. It does so via two main pathways: (i) decreasing the size of native refugia, which reduces seed production and increases local extinction, and (ii) eroding the dispersal permeability of the matrix between refugia, which reduces their connectivity. Even when native plant extinction is the deterministic outcome of invasion, the time to extinction can be on the order of hundreds of years. We conclude that the relatively short time since invasion in many parts of the world is insufficient to observe the full impact of plant invasions on native biodiversity.

  2. Mass Extinctions in Earth's History

    NASA Astrophysics Data System (ADS)

    Ward, P. D.

    2002-12-01

    Mass extinctions are short intervals of elevated species death. Possible causes of Earth's mass extinctions are both external (astronomical) and internal (tectonic and biotic changes from planetary mechanisms). Paleontologists have identified five "major" mass extinctions (>50 die-off in less than a million years) and more than 20 other minor events over the past 550 million years. Earlier major extinction events undoubtedly also occurred, but we have no fossil record; these were probably associated with, for example, the early heavy bombardment that cleared out the solar system, the advent of oxygen in the atmosphere, and various "snowball Earth" events. Mass extinctions are viewed as both destructive (species death ) and constructive, in that they allow evolutionary innovation in the wake of species disappearances. From an astrobiological perspective, mass extinctions must be considered as able both to reduce biodiversity and even potentially end life on any planet. Of the five major mass extinctions identified on Earth, only one (the Cretaceous/Tertiary event 65 million years ago that famously killed off the dinosaurs ) is unambiguously related to the impact of an asteroid or comet ( 10-km diameter). The Permian/Triassic (250 Myr ago) and Triassic/Jurassic (202 Myr ago) events are now the center of debate between those favoring impact and those suggesting large volume flooding by basaltic lavas. The final two events, Ordovician (440 Myr ago) and Devonian (370 Myr ago) have no accepted causal mechanisms.

  3. The learning of fear extinction.

    PubMed

    Furini, Cristiane; Myskiw, Jociane; Izquierdo, Ivan

    2014-11-01

    Recent work on the extinction of fear-motivated learning places emphasis on its putative circuitry and on its modulation. Extinction is the learned inhibition of retrieval of previously acquired responses. Fear extinction is used as a major component of exposure therapy in the treatment of fear memories such as those of the posttraumatic stress disorder (PTSD). It is initiated and maintained by interactions between the hippocampus, basolateral amygdala and ventromedial prefrontal cortex, which involve feedback regulation of the latter by the other two areas. Fear extinction depends on NMDA receptor activation. It is positively modulated by d-serine acting on the glycine site of NMDA receptors and blocked by AP5 (2-amino-5-phosphono propionate) in the three structures. In addition, histamine acting on H2 receptors and endocannabinoids acting on CB1 receptors in the three brain areas mentioned, and muscarinic cholinergic fibers from the medial septum to hippocampal CA1 positively modulate fear extinction. Importantly, fear extinction can be made state-dependent on circulating epinephrine, which may play a role in situations of stress. Exposure to a novel experience can strongly enhance the consolidation of fear extinction through a synaptic tagging and capture mechanism; this may be useful in the therapy of states caused by fear memory like PTSD.

  4. Extinction in young massive clusters

    NASA Astrophysics Data System (ADS)

    De Marchi, Guido; Panagia, Nino

    2016-01-01

    Up to ages of ~100 Myr, massive clusters are still swamped in large amounts of gas and dust, causing considerable and uneven levels of extinction. At the same time, large grains (ices?) produced by type II supernovae profoundly alter the interstellar medium (ISM), thus resulting in extinction properties very different from those of the diffuse ISM. To obtain physically meaningful parameters of stars (luminosities, effective temperatures, masses, ages, etc.) we must understand and measure the local extinction law. We have developed a powerful method to unambiguously determine the extinction law everywhere across a cluster field, using multi-band photometry of red giant stars belonging to the red clump (RC) and are applying it to young massive clusters in the Local Group. In the Large Magellanic Cloud, with about 20 RC stars per arcmin2, for each field we can easily derive an accurate extinction curve over the entire wavelength range of the photometry. As an example, we present the extinction law of the Tarantula nebula (30 Dor) based on thousands of stars observed as part of the Hubble Tarantula Treasury Project. We discuss how the incautious adoption of the Milky Way extinction law in the analysis of massive star forming regions may lead to serious underestimates of the fluxes and of the star formation rates by factors of 2 or more.

  5. SAGE II Measurements of Stratospheric Aerosol Properties at Non-Volcanic Levels

    NASA Technical Reports Server (NTRS)

    Thomason, Larry W.; Burton, Sharon P.; Luo, Bei-Ping; Peter, Thomas

    2008-01-01

    Since 2000, stratospheric aerosol levels have been relatively stable and at the lowest levels observed in the historical record. Given the challenges of making satellite measurements of aerosol properties at these levels, we have performed a study of the sensitivity of the product to the major components of the processing algorithm used in the production of SAGE II aerosol extinction measurements and the retrieval process that produces the operational surface area density (SAD) product. We find that the aerosol extinction measurements, particularly at 1020 nm, remain robust and reliable at the observed aerosol levels. On the other hand, during background periods, the SAD operational product has an uncertainty of at least a factor of 2 during due to the lack of sensitivity to particles with radii less than 100 nm.

  6. Airborne High Spectral Resolution Lidar Aerosol Measurements during MILAGRO and TEXAQS/GOMACCS

    NASA Technical Reports Server (NTRS)

    Ferrare, Richard; Hostetler, Chris; Hair, John; Cook Anthony; Harper, David; Burton, Sharon; Clayton, Marian; Clarke, Antony; Russell, Phil; Redemann, Jens

    2007-01-01

    Two1 field experiments conducted during 2006 provided opportunities to investigate the variability of aerosol properties near cities and the impacts of these aerosols on air quality and radiative transfer. The Megacity Initiative: Local and Global Research Observations (MILAGRO) /Megacity Aerosol Experiment in Mexico City (MAX-MEX)/Intercontinental Chemical Transport Experiment-B (INTEX-B) joint experiment conducted during March 2006 investigated the evolution and transport of pollution from Mexico City. The Texas Air Quality Study (TEXAQS)/Gulf of Mexico Atmospheric Composition and Climate Study (GoMACCS) (http://www.al.noaa.gov/2006/) conducted during August and September 2006 investigated climate and air quality in the Houston/Gulf of Mexico region. During both missions, the new NASA Langley airborne High Spectral Resolution Lidar (HSRL) was deployed on the NASA Langley B200 King Air aircraft and measured profiles of aerosol extinction, backscattering, and depolarization to: 1) characterize the spatial and vertical distributions of aerosols, 2) quantify aerosol extinction and optical thickness contributed by various aerosol types, 3) investigate aerosol variability near clouds, 4) evaluate model simulations of aerosol transport, and 5) assess aerosol optical properties derived from a combination of surface, airborne, and satellite measurements.

  7. Parameter sensitivity study of Arctic aerosol vertical distribution in CAM5

    NASA Astrophysics Data System (ADS)

    Jiao, C.; Flanner, M.

    2015-12-01

    Arctic surface temperature response to light-absorbing aerosols (black carbon, brown carbon and dust) depends strongly on their vertical distributions. Improving model simulations of three dimensional aerosol fields in the remote Arctic region will therefore lead to improved projections of the climate change caused by aerosol emissions. In this study, we investigate how different physical parameterizations in the Community Atmosphere Model version 5 (CAM5) influence the simulated vertical distribution of Arctic aerosols. We design experiments to test the sensitivity of the simulated aerosol fields to perturbations of selected aerosol process-related parameters in the Modal Aerosol Module with seven lognormal modes (MAM7), such as those govern aerosol aging, in-cloud and below-cloud scavenging, aerosol hygroscopicity and so on. The simulations are compared with observed aerosol vertical distributions and total optical depth to assess model performance and quantify uncertainties associated with these model parameterizations. Observations applied here include Arctic aircraft measurements of black carbon and sulfate vertical profiles, along with Aerosol Robotic Network (AERONET) optical depth measurements. We also assess the utility of using High Spectral Resolution Lidar (HSRL) measurements from the ARM Barrow site to infer vertical profiles of aerosol extinction. The sensitivity study explored here will provide guidance for optimizing global aerosol simulations.

  8. Aerosol classification using airborne High Spectral Resolution Lidar measurements - methodology and examples

    NASA Astrophysics Data System (ADS)

    Burton, S. P.; Ferrare, R. A.; Hostetler, C. A.; Hair, J. W.; Rogers, R. R.; Obland, M. D.; Butler, C. F.; Cook, A. L.; Harper, D. B.; Froyd, K. D.

    2012-01-01

    The NASA Langley Research Center (LaRC) airborne High Spectral Resolution Lidar (HSRL) on the NASA B200 aircraft has acquired extensive datasets of aerosol extinction (532 nm), aerosol optical depth (AOD) (532 nm), backscatter (532 and 1064 nm), and depolarization (532 and 1064 nm) profiles during 18 field missions that have been conducted over North America since 2006. The lidar measurements of aerosol intensive parameters (lidar ratio, depolarization, backscatter color ratio, and spectral depolarization ratio) are shown to vary with location and aerosol type. A methodology based on observations of known aerosol types is used to qualitatively classify the extensive set of HSRL aerosol measurements into eight separate types. Several examples are presented showing how the aerosol intensive parameters vary with aerosol type and how these aerosols are classified according to this new methodology. The HSRL-based classification reveals vertical variability of aerosol types during the NASA ARCTAS field experiment conducted over Alaska and northwest Canada during 2008. In two examples derived from flights conducted during ARCTAS, the HSRL classification of biomass burning smoke is shown to be consistent with aerosol types derived from coincident airborne in situ measurements of particle size and composition. The HSRL retrievals of AOD and inferences of aerosol types are used to apportion AOD to aerosol type; results of this analysis are shown for several experiments.

  9. Aerosol classification using airborne High Spectral Resolution Lidar measurements - methodology and examples

    NASA Astrophysics Data System (ADS)

    Burton, S. P.; Ferrare, R. A.; Hostetler, C. A.; Hair, J. W.; Rogers, R. R.; Obland, M. D.; Butler, C. F.; Cook, A. L.; Harper, D. B.; Froyd, K. D.

    2011-09-01

    The NASA Langley Research Center (LaRC) airborne High Spectral Resolution Lidar (HSRL) on the NASA B200 aircraft has acquired extensive datasets of aerosol extinction (532 nm), aerosol optical thickness (AOT) (532 nm), backscatter (532 and 1064 nm), and depolarization (532 and 1064 nm) profiles during 18 field missions that have been conducted over North America since 2006. The lidar measurements of aerosol intensive parameters (lidar ratio, depolarization, backscatter color ratio, and spectral depolarization ratio) are shown to vary with location and aerosol type. A methodology based on observations of known aerosol types is used to qualitatively classify the extensive set of HSRL aerosol measurements into eight separate types. Several examples are presented showing how the aerosol intensive parameters vary with aerosol type and how these aerosols are classified according to this new methodology. The HSRL-based classification reveals vertical variability of aerosol types during the NASA ARCTAS field experiment conducted over Alaska and northwest Canada during 2008. In two examples derived from flights conducted during ARCTAS, the HSRL classification of biomass burning smoke is shown to be consistent with aerosol types derived from coincident airborne in situ measurements of particle size and composition. The HSRL retrievals of AOT and inferences of aerosol types are used to apportion AOT to aerosol type; results of this analysis are shown for several experiments.

  10. Microphysical, chemical and optical aerosol properties in the Baltic Sea region

    NASA Astrophysics Data System (ADS)

    Kikas, Ülle; Reinart, Aivo; Pugatshova, Anna; Tamm, Eduard; Ulevicius, Vidmantas

    2008-11-01

    The microphysical structure, chemical composition and prehistory of aerosol are related to the aerosol optical properties and radiative effect in the UV spectral range. The aim of this work is the statistical mapping of typical aerosol scenarios and adjustment of regional aerosol parameters. The investigation is based on the in situ measurements in Preila (55.55° N, 21.00° E), Lithuania, and the AERONET data from the Gustav Dalen Tower (58 N, 17 E), Sweden. Clustering of multiple characteristics enabled to distinguish three aerosol types for clear-sky periods: 1) clean maritime-continental aerosol; 2) moderately polluted maritime-continental aerosol; 3) polluted continental aerosol. Differences between these types are due to significant differences in aerosol number and volume concentration, effective radius of volume distribution, content of SO 4- ions and Black Carbon, as well as different vertical profiles of atmospheric relative humidity. The UV extinction, aerosol optical depth (AOD) and the Ångstrom coefficient α increased with the increasing pollution. The value α = 1.96 was observed in the polluted continental aerosol that has passed over central and eastern Europe and southern Russia. Reduction of the clear-sky UV index against the aerosol-free atmosphere was of 4.5%, 27% and 41% for the aerosol types 1, 2 and 3, respectively.

  11. New theories about ancient extinctions

    USGS Publications Warehouse

    Spall, H.

    1986-01-01

    But all this may be changing. Mass extinctions have been very much in the news in the last few years, triggered in large part by the proposal that the extinction of the dinosaurs and marine animals was caused by a catastrophic collision between the Earth and an extra-terrestrial body (bolide). Recently an equally contentious suggestion has been made that mass extinctions have swept the Earth every 26 to 31 million years for at least the last 250 million years-caused by encounters with some kind of extra-terrestrial object such as one of the asteroids or the comets. 

  12. Evaluation of Daytime Measurements of Aerosols and Water Vapor made by an Operational Raman Lidar over the Southern Great Plains

    NASA Technical Reports Server (NTRS)

    Ferrare, Richard; Turner, David; Clayton, Marian; Schmid, Beat; Covert, David; Elleman, Robert; Orgren, John; Andrews, Elisabeth; Goldsmith, John E. M.; Jonsson, Hafidi

    2006-01-01

    Raman lidar water vapor and aerosol extinction profiles acquired during the daytime over the Department of Energy (DOE) Atmospheric Radiation Measurement (ARM) Southern Great Plains (SGP) site in northern Oklahoma (36.606 N, 97.50 W, 315 m) are evaluated using profiles measured by in situ and remote sensing instruments deployed during the May 2003 Aerosol Intensive Operations Period (IOP). The automated algorithms used to derive these profiles from the Raman lidar data were first modified to reduce the adverse effects associated with a general loss of sensitivity of the Raman lidar since early 2002. The Raman lidar water vapor measurements, which are calibrated to match precipitable water vapor (PWV) derived from coincident microwave radiometer (MWR) measurements were, on average, 5-10% (0.3-0.6 g/m(exp 3) higher than the other measurements. Some of this difference is due to out-of-date line parameters that were subsequently updated in the MWR PWV retrievals. The Raman lidar aerosol extinction measurements were, on average, about 0.03 km(exp -1) higher than aerosol measurements derived from airborne Sun photometer measurements of aerosol optical thickness and in situ measurements of aerosol scattering and absorption. This bias, which was about 50% of the mean aerosol extinction measured during this IOP, decreased to about 10% when aerosol extinction comparisons were restricted to aerosol extinction values larger than 0.15 km(exp -1). The lidar measurements of the aerosol extinction/backscatter ratio and airborne Sun photometer measurements of the aerosol optical thickness were used along with in situ measurements of the aerosol size distribution to retrieve estimates of the aerosol single scattering albedo (omega(sub o)) and the effective complex refractive index. Retrieved values of omega(sub o) ranged from (0.91-0.98) and were in generally good agreement with omega(sub o) derived from airborne in situ measurements of scattering and absorption. Elevated aerosol

  13. AeroCom INSITU Project: Comparing modeled and measured aerosol optical properties

    NASA Astrophysics Data System (ADS)

    Andrews, Elisabeth; Schmeisser, Lauren; Schulz, Michael; Fiebig, Markus; Ogren, John; Bian, Huisheng; Chin, Mian; Easter, Richard; Ghan, Steve; Kokkola, Harri; Laakso, Anton; Myhre, Gunnar; Randles, Cynthia; da Silva, Arlindo; Stier, Phillip; Skeie, Ragnehild; Takemura, Toshihiko; van Noije, Twan; Zhang, Kai

    2016-04-01

    AeroCom, an open international collaboration of scientists seeking to improve global aerosol models, recently initiated a project comparing model output to in-situ, surface-based measurements of aerosol optical properties. The model/measurement comparison project, called INSITU, aims to evaluate the performance of a suite of AeroCom aerosol models with site-specific observational data in order to inform iterative improvements to model aerosol modules. Surface in-situ data has the unique property of being traceable to physical standards, which is an asset in accomplishing the overall goal of bettering the accuracy of aerosols processes and the predicative capability of global climate models. Here we compare dry, in-situ aerosol scattering and absorption data from ~75 surface, in-situ sites from various global aerosol networks (including NOAA, EUSAAR/ACTRIS and GAW) with a simulated optical properties from a suite of models participating in the AeroCom project. We report how well models reproduce aerosol climatologies for a variety of time scales, aerosol characteristics and behaviors (e.g., aerosol persistence and the systematic relationships between aerosol optical properties), and aerosol trends. Though INSITU is a multi-year endeavor, preliminary phases of the analysis suggest substantial model biases in absorption and scattering coefficients compared to surface measurements, though the sign and magnitude of the bias varies with location. Spatial patterns in the biases highlight model weaknesses, e.g., the inability of models to properly simulate aerosol characteristics at sites with complex topography. Additionally, differences in modeled and measured systematic variability of aerosol optical properties suggest that some models are not accurately capturing specific aerosol behaviors, for example, the tendency of in-situ single scattering albedo to decrease with decreasing aerosol extinction coefficient. The endgoal of the INSITU project is to identify specific

  14. Detection and quantification of water-based aerosols using active open-path FTIR

    PubMed Central

    Kira, Oz; Linker, Raphael; Dubowski, Yael

    2016-01-01

    Aerosols have a leading role in many eco-systems and knowledge of their properties is critical for many applications. This study suggests using active Open-Path Fourier Transform Infra-Red (OP-FTIR) spectroscopy for quantifying water droplets and solutes load in the atmosphere. The OP-FTIR was used to measure water droplets, with and without solutes, in a 20 m spray tunnel. Three sets of spraying experiments generated different hydrosols clouds: (1) tap water only, (2) aqueous ammonium sulfate (0.25–3.6%wt) and (3) aqueous ethylene glycol (0.47–2.38%wt). Experiment (1) yielded a linear relationship between the shift of the extinction spectrum baseline and the water load in the line-of-sight (LOS) (R2 = 0.984). Experiment (2) also yielded a linear relationship between the integrated extinction in the range of 880–1150 cm−1 and the ammonium sulfate load in the LOS (R2 = 0.972). For the semi-volatile ethylene glycol (experiment 3), present in the gas and condense phases, quantification was much more complex and two spectral approaches were developed: (1) according to the linear relationship from the first experiment (determination error of 8%), and (2) inverse modeling (determination error of 57%). This work demonstrates the potential of the OP-FTIR for detecting clouds of water-based aerosols and for quantifying water droplets and solutes at relatively low concentrations. PMID:27121498

  15. Aerosol composition and variability in the Baltimore-Washington, DC region

    NASA Astrophysics Data System (ADS)

    Beyersdorf, A. J.; Ziemba, L. D.; Chen, G.; Corr, C. A.; Crawford, J. H.; Diskin, G. S.; Moore, R. H.; Thornhill, K. L.; Winstead, E. L.; Anderson, B. E.

    2015-08-01

    In order to utilize satellite-based aerosol measurements for the determination of air quality, the relationship between aerosol optical properties (wavelength-dependent, column-integrated extinction measured by satellites) and mass measurements of aerosol loading (PM2.5 used for air quality monitoring) must be understood. This connection varies with many factors including those specific to the aerosol type, such as composition, size and hygroscopicity, and to the surrounding atmosphere, such as temperature, relative humidity (RH) and altitude, all of which can vary spatially and temporally. During the DISCOVER-AQ (Deriving Information on Surface conditions from Column and Vertically Resolved Observations Relevant to Air Quality) project, extensive in-situ atmospheric profiling in the Baltimore, MD-Washington, DC region was performed during fourteen flights in July 2011. Identical flight plans and profile locations throughout the project provide meaningful statistics for determining the variability in and correlations between aerosol loading, composition, optical properties and meteorological conditions. Measured water-soluble aerosol mass was composed primarily of ammonium sulfate (campaign average of 32 %) and organics (57 %). A distinct difference in composition was observed with high-loading days having a proportionally larger percentage of ammonium sulfate (up to 49 %) due to transport from the Ohio River Valley. This composition shift caused a change in the aerosol water-uptake potential (hygroscopicity) such that higher relative contributions of ammonium sulfate increased the bulk aerosol hygroscopic