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Sample records for aerosol properties measured

  1. 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.

  2. International Workshop on Stratospheric Aerosols: Measurements, Properties, and Effects

    NASA Technical Reports Server (NTRS)

    Pueschel, Rudolf F. (Editor)

    1991-01-01

    Following a mandate by the International Aerosol Climatology Program under the auspices of International Association of Meteorology and Atmospheric Physics International Radiation Commission, 45 scientists from five nations convened to discuss relevant issues associated with the measurement, properties, and effects of stratospheric aerosols. A summary is presented of the discussions on formation and evolution, transport and fate, effects on climate, role in heterogeneous chemistry, and validation of lidar and satellite remote sensing of stratospheric aerosols. Measurements are recommended of the natural (background) and the volcanically enhanced aerosol (sulfuric acid and silica particles), the exhaust of shuttle, civil aviation and supersonic aircraft operations (alumina, soot, and ice particles), and polar stratospheric clouds (ice, condensed nitric and hydrochloric acids).

  3. Measuring Aerosol Optical Properties with the Ozone Monitoring Instrument (OMI)

    NASA Technical Reports Server (NTRS)

    Veefkind, J. P.; Torres, O.; Syniuk, A.; Decae, R.; deLeeuw, G.

    2003-01-01

    The Ozone Monitoring Instrument (OMI) is the Dutch-Finnish contribution to the NASA EOS-Aura mission scheduled for launch in January 2004. OM1 is an imaging spectrometer that will measure the back-scattered Solar radiance between 270 an 500 nm. With its relatively high spatial resolution (13x24 sq km at nadir) and daily global coverage. OM1 will make a major contribution to our understanding of atmospheric chemistry and to climate research. OM1 will provide data continuity with the TOMS instruments. One of the pleasant surprises of the TOMS data record was its information on aerosol properties. First, only the absorbing aerosol index, which is sensitive to elevated lay- ers of aerosols such as desert dust and smoke aerosols, was derived. Recently these methods were further improved to yield aerosol optical thickness and single scattering albedo over land and ocean for 19 years of TOMS data (1979-1992,1997-2002), making it one of the longest and most valuable time series for aerosols presently available. Such long time series are essential to quantify the effect of aerosols on the Earth& climate. The OM1 instrument is better suited to measure aerosols than the TOMS instruments because of the smaller footprint, and better spectral coverage. The better capabilities of OMI will enable us to provide an improved aerosol product, but the knowledge will also be used for further analysis of the aerosol record from TOMS. The OM1 aerosol product that is currently being developed for OM1 combines the TOMS experience and the multi-spectral techniques that are used in the visible and near infrared. The challenge for this new product is to provide aerosol optical thickness and single scattering albedo from the near ultraviolet to the visible (330-500 nm) over land and ocean. In this presentation the methods for deriving the OM1 aerosol product will be presented. Part of these methods developed for OM1 can already be applied to TOMS data and results of such analysis will be shown.

  4. Evaluation of Aerosol Properties in GCMs using Satellite Measurements

    NASA Astrophysics Data System (ADS)

    Wang, Y.; Jiang, J. H.; Su, H.; Zhang, H.

    2015-12-01

    Atmospheric aerosols from natural or anthropogenic sources have profound impacts on the regional and global climate. Currently the radiative forcing of aerosols predicted by global climate models remains highly uncertain, representing the largest uncertainty in climate predictions. The uncertainty mainly arises from the complicated aerosol chemical and physical properties, coarse emission inventories for pre-cursor gases as well as unrealistic representations of aerosol activation and cloud processing in global climate models. In this study, we will utilize multiple satellite measurements including MODIS, MISR and CALIPSO to quantitatively evaluate aerosol simulations from climate models. Our analyses show that the global means in AOD climatology from NCAR CAM5 and GFDL AM3 simulations are comparable with satellite measurements. However, the overall correlation coefficient between the AOD spatial patterns from CAM5 and satellite is only 0.4. Moreover, at finer scales, the magnitude of AOD in CAM5 is much lower than satellite measurements for most of the non-dust regions, especially over East Asia. GFDL AM3 shows better AOD simulations over East Asia. The underestimated AOD over remote maritime areas in CAM5 was attributed to the unrealistic wet removal processes in convective clouds of CAM5. Over continents, biases on AOD could stem from underestimations in the emissions inventory and unresolved sub-grid variations of relative humidity due to the model's coarse resolution. Uncertainty from emission inventory over developing countries in East Asia will be assessed using the newly updated Regional Emission inventory in Asia (REAS) and Multi-resolution Emission Inventory in China (MEIC) in the model simulations.

  5. AEROSOL AND GAS MEASUREMENT

    EPA Science Inventory

    Measurements provide fundamental information for evaluating and managing the impact of aerosols on air quality. Specific measurements of aerosol concentration and their physical and chemical properties are required by different users to meet different user-community needs. Befo...

  6. Ground-based Network and Supersite Measurements for Studying Aerosol Properties and Aerosol-Cloud Interactions

    NASA Technical Reports Server (NTRS)

    Tsay, Si-Chee; Holben, Brent N.

    2008-01-01

    From radiometric principles, it is expected that the retrieved properties of extensive aerosols and clouds from reflected/emitted measurements by satellite (and/or aircraft) should be consistent with those retrieved from transmitted/emitted radiance observed at the surface. Although space-borne remote sensing observations contain large spatial domain, they are often plagued by contamination of surface signatures. Thus, ground-based in-situ and remote-sensing measurements, where signals come directly from atmospheric constituents, the sun, and the Earth-atmosphere interactions, provide additional information content for comparisons that confirm quantitatively the usefulness of the integrated surface, aircraft, and satellite datasets. The development and deployment of AERONET (AErosol RObotic NETwork) sunphotometer network and SMART-COMMIT (Surface-sensing Measurements for Atmospheric Radiative Transfer - Chemical, Optical & Microphysical Measurements of In-situ Troposphere) mobile supersite are aimed for the optimal utilization of collocated ground-based observations as constraints to yield higher fidelity satellite retrievals and to determine any sampling bias due to target conditions. To characterize the regional natural and anthropogenic aerosols, AERONET is an internationally federated network of unique sunphotometry that contains more than 250 permanent sites worldwide. Since 1993, there are more than 480 million aerosol optical depth observations and about 15 sites have continuous records longer than 10 years for annual/seasonal trend analyses. To quantify the energetics of the surface-atmosphere system and the atmospheric processes, SMART-COMMIT instrument into three categories: flux radiometer, radiance sensor and in-situ probe. Through participation in many satellite remote-sensing/retrieval and validation projects over eight years, SMART-COMMIT have gradually refine( and been proven vital for field deployment. In this paper, we will demonstrate the

  7. Retrieval of stratospheric aerosol size distributions and integral properties from simulated lidar backscatter measurements.

    PubMed

    Yue, G K

    2000-10-20

    A new approach for retrieving aerosol properties from extinction spectra is extended to retrieve aerosol properties from lidar backscatter measurements. In this method it is assumed that aerosol properties are expressed as a linear combination of backscatters at three or fewer wavelengths commonly used in lidar measurements. The coefficients in the weighted linear combination are obtained by minimization of the retrieval error averaged for a set of testing size distributions. The formulas can be used easily by investigators to retrieve aerosol properties from lidar backscatter measurements such as the Lidar In-Space Technology Experiment and Pathfinder Instruments for Clouds and Aerosols Spaceborne Observations.

  8. 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

  9. Vertical Profiles of Cloud Condensation Nuclei, Condensation Nuclei, Optical Aerosol, Aerosol Optical Properties, and Aerosol Volatility Measured from Balloons

    NASA Technical Reports Server (NTRS)

    Deshler, T.; Snider, J. R.; Vali, G.

    1998-01-01

    Under the support of this grant a balloon-borne gondola containing a variety of aerosol instruments was developed and flown from Laramie, Wyoming, (41 deg N, 105 deg W) and from Lauder, New Zealand (45 deg S, 170 deg E). The gondola includes instruments to measure the concentrations of condensation nuclei (CN), cloud condensation nuclei (CCN), optically detectable aerosol (OA.) (r greater than or equal to 0.15 - 2.0 microns), and optical scattering properties using a nephelometer (lambda = 530 microns). All instruments sampled from a common inlet which was heated to 40 C on ascent and to 160 C on descent. Flights with the CN counter, OA counter, and nephelometer began in July 1994. The CCN counter was added in November 1994, and the engineering problems were solved by June 1995. Since then the flights have included all four instruments, and were completed in January 1998. Altogether there were 20 flights from Laramie, approximately 5 per year, and 2 from Lauder. Of these there were one or more engineering problems on 6 of the flights from Laramie, hence the data are somewhat limited on those 6 flights, while a complete data set was obtained from the other 14 flights. Good CCN data are available from 12 of the Laramie flights. The two flights from Lauder in January 1998 were successful for all measurements. The results from these flights, and the development of the balloon-bome CCN counter have formed the basis for five conference presentations. The heated and unheated CN and OA measurements have been used to estimate the mass fraction of the aerosol volatile, while comparisons of the nephelometer measurements were used to estimate the light scattering, associated with the volatile aerosol. These estimates were calculated for 0.5 km averages of the ascent and descent data between 2.5 km and the tropopause, near 11.5 km.

  10. Retrieval of Aerosol Properties from Multi-Spectral Extinction Measurements

    NASA Technical Reports Server (NTRS)

    Lacis, Andrew A.

    1999-01-01

    The direct-beam spectral extinction of solar radiation contains information on atmospheric composition in a form that is essentially free from the data analysis complexities that often arise from multiple scattering. Ground based Multi-Filter Shadowband Radiometer (MFRSR) measurements provide such information for the vertical atmospheric column path, while solar occultation measurements from a satellite platform provide horizontal slices through the atmosphere. We describe application of a Multi-Spectral Atmospheric Column Extinction (MACE) analysis technique used to analyze MFRSR data also to occultation measurements made by SAGE II. For analysis, we select the 1985 Nevado del Ruiz volcanic eruption period to retrieve atmospheric profiles of ozone and NO2, and changes in the stratospheric aerosol size and optical depth. The time evolution of volcanic aerosol serves as a passive tracer to study stratospheric dynamics, and changes in particle size put constraints on the sulfur chemistry modeling of volcanic aerosols. Paper presented at The '99 Kyoto Aerosol-Cloud Workshop, held Dec 1-3, 1999, Kyoto, Japan

  11. New algorithm to derive the microphysical properties of the aerosols from lidar measurements using OPAC aerosol classification schemes

    NASA Astrophysics Data System (ADS)

    Talianu, Camelia; Labzovskii, Lev; Toanca, Florica

    2014-05-01

    This paper presents a new method to retrieve the aerosol complex refractive index and effective radius from multiwavelength lidar data, using an integrated model-measurement approach. In the model, aerosols are assumed to be a non-spherical ensemble of internally mixed components, with variable proportions. OPAC classification schemes and basic components are used to calculate the microphysical properties, which are then fed into the T-matrix calculation code to generate the corresponding optical parameters. Aerosol intensive parameters (lidar ratios, extinction and backscatter Angstrom coefficients, and linear particle depolarization ratios) are computed at the altitude of the aerosol layers determined from lidar measurements, and iteratively compared to the values obtained by simulation for a certain aerosol type, for which the critical component's proportion in the overall mixture is varied. Microphysical inversion based on the Truncated Singular Value Decomposition (TSVD) algorithm is performed for selected cases of spherical aerosols, and comparative results of the two methods are shown. Keywords: Lidar, aerosols, Data inversion, Optical parameters, Complex Refractive Index Acknowledgments: This work has been supported by grants of the Romanian National Authority for Scientific Research, Programme for Research- Space Technology and Advanced Research - STAR, project numbers 38/2012 - CAPESA and 55/2013 - CARESSE, and by the European Community's FP7-INFRASTRUCTURES-2010-1 under grant no. 262254 - ACTRIS and by the European Community's FP7-PEOPLE-2011-ITN under grant no. 289923 - ITARS

  12. Vertical distribution of aerosol optical properties based on aircraft measurements over the Loess Plateau in China.

    PubMed

    Li, Junxia; Liu, Xingang; Yuan, Liang; Yin, Yan; Li, Zhanqing; Li, Peiren; Ren, Gang; Jin, Lijun; Li, Runjun; Dong, Zipeng; Li, Yiyu; Yang, Junmei

    2015-08-01

    Vertical distributions of aerosol optical properties based on aircraft measurements over the Loess Plateau were measured for the first time during a summertime aircraft campaign, 2013 in Shanxi, China. Data from four flights were analyzed. The vertical distributions of aerosol optical properties including aerosol scattering coefficients (σsc), absorption coefficients (σab), Angström exponent (α), single scattering albedo (ω), backscattering ratio (βsc), aerosol mass scattering proficiency (Qsc) and aerosol surface scattering proficiency (Qsc(')) were obtained. The mean statistical values of σsc were 77.45 Mm(-1) (at 450 nm), 50.72 Mm(-1) (at 550n m), and 32.02 Mm(-1) (at 700 nm). The mean value of σab was 7.62 Mm(-1) (at 550 nm). The mean values of α, βsc and ω were 1.93, 0.15, and 0.91, respectively. Aerosol concentration decreased with altitude. Most effective diameters (ED) of aerosols were less than 0.8 μm. The vertical profiles of σsc,, α, βsc, Qsc and Qsc(') showed that the aerosol scattering properties at lower levels contributed the most to the total aerosol radiative forcing. Both α and βsc had relatively large values, suggesting that most aerosols in the observational region were small particles. The mean values of σsc, α, βsc, Qsc, Qsc('), σab and ω at different height ranges showed that most of the parameters decreased with altitude. The forty-eight hour backward trajectories of air masses during the observation days indicated that the majority of aerosols in the lower level contributed the most to the total aerosol loading, and most of these particles originated from local or regional pollution emissions.

  13. 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.

  14. 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

  15. Intercomparison and closure calculations using measurements of aerosol species and optical properties during the Yosemite Aerosol Characterization Study

    NASA Astrophysics Data System (ADS)

    Malm, William C.; Day, Derek E.; Carrico, Christian; Kreidenweis, Sonia M.; Collett, Jeffrey L.; McMeeking, Gavin; Lee, Taehyoung; Carrillo, Jacqueline; Schichtel, Bret

    2005-07-01

    Physical and optical properties of inorganic aerosols have been extensively studied, but less is known about carbonaceous aerosols, especially as they relate to the non-urban settings such as our nation's national parks and wilderness areas. Therefore an aerosol characterization study was conceived and implemented at one national park that is highly impacted by carbonaceous aerosols, Yosemite. The primary objective of the study was to characterize the physical, chemical, and optical properties of a carbon-dominated aerosol, including the ratio of total organic matter weight to organic carbon, organic mass scattering efficiencies, and the hygroscopic characteristics of a carbon-laden ambient aerosol, while a secondary objective was to evaluate a variety of semi-continuous monitoring systems. Inorganic ions were characterized using 24-hour samples that were collected using the URG and Interagency Monitoring of Protected Visual Environments (IMPROVE) monitoring systems, the micro-orifice uniform deposit impactor (MOUDI) cascade impactor, as well as the semi-continuous particle-into-liquid sampler (PILS) technology. Likewise, carbonaceous material was collected over 24-hour periods using IMPROVE technology along with the thermal optical reflectance (TOR) analysis, while semi-continuous total carbon concentrations were measured using the Rupprecht and Patashnick (R&P) instrument. Dry aerosol number size distributions were measured using a differential mobility analyzer (DMA) and optical particle counter, scattering coefficients at near-ambient conditions were measured with nephelometers fitted with PM10 and PM2.5 inlets, and "dry" PM2.5 scattering was measured after passing ambient air through Perma Pure Nafion® dryers. In general, the 24-hour "bulk" measurements of various aerosol species compared more favorably with each other than with the semi-continuous data. Semi-continuous sulfate measurements correlated well with the 24-hour measurements, but were biased low by

  16. Aerosol Properties and Processes: A Path from Field and Laboratory Measurements to Global Climate Models

    SciTech Connect

    Ghan, Steven J.; Schwartz, Stephen E.

    2007-07-01

    Aerosols exert a substantial influence on climate and climate change through a variety of complex mechanisms. Consequently there is a need to represent aerosol effects in global climate models, and models have begun to include representations of these effects. However, the treatment of aerosols in current global climate models is presently highly simplified, omitting many important processes and feedbacks. Consequently there is need for substantial improvement. Here we describe the U. S. Department of Energy strategy for improving the treatment of aerosol properties and processes in global climate models. The strategy begins with a foundation of field and laboratory measurements that provide the basis for modules of selected aerosol properties and processes. These modules are then integrated in regional aerosol models, which are evaluated by comparing with field measurements. Issues of scale are then addressed so that the modules can be applied to global aerosol models, which are evaluated by comparing with global satellite measurements. Finally, the validated set of modules are applied to global climate models for multi-century simulations. This strategy can be applied to successive generations of global climate models.

  17. Atmospheric aerosols: Their Optical Properties and Effects

    NASA Technical Reports Server (NTRS)

    1976-01-01

    Measured properties of atmospheric aerosol particles are presented. These include aerosol size frequency distribution and complex retractive index. The optical properties of aerosols are computed based on the presuppositions of thermodynamic equilibrium and of Mie-theory.

  18. LIDAR Measurements of the Vertical Distribution of Aerosol Optical and Physical Properties over Central Asia

    EPA Science Inventory

    The vertical structure of aerosol optical and physical properties was measured by Lidar in Eastern Kyrgyzstan, Central Asia, from June 2008 to May 2009. Lidar measurements were supplemented with surface-based measurements of PM2.5 and PM10 mass and chemical ...

  19. An algorithm for retrieving fine and coarse aerosol microphysical properties from AERONET-type photopolarimetric measurements

    NASA Astrophysics Data System (ADS)

    Xu, X.; Wang, J.; Zeng, J.; Spurr, R. J. D.; Liu, X.; Dubovik, O.; Li, Z.; Li, L.; Holben, B. N.; Mishchenko, M. I.

    2014-12-01

    A new retrieval algorithm has been developed to retrieve both fine and coarse modal aerosol properties from multi-spectral and multi-angular solar polarimetric radiation fields such as those measured by the AErosol RObotic NETwork (AERONET) but with additional channels of polarization observations (hereafter AEROENT-type measurements). Most AERONET sites lack the capability to measure light polarization, though a few measure polarization only at 870 nm. From both theory and real cases, we show that adding multi-spectral polarization data can allow a mode-resolved inversion of aerosol microphysical parameters. In brief, the retrieval algorithm incorporates AERONET-type measurements in conjunction with advanced vector radiative transfer model specifically designed for studying the inversion problems in aerosol remote sensing. It retrieves aerosol parameters associated to a bi-lognormal particle size distribution (PSD) including aerosol volume concentrations, effective radius and variance, and complex indices of aerosol refraction. Our algorithm differs from the current AERONET inversion algorithm in two major aspects. First, it retrieves effective radius and variance and total volume by assuming a bi-modal lognormal PSD, while AERONET one retrieves aerosol volumes of 22 size bins. Second, our algorithm retrieves spectral refractive indices for both fine and coarse modes. Mode-resolved refractive indices can improve the estimate of single scattering albedo (SSA) for each mode, which also benefits the evaluation for satellite products and chemistry transport models. While bi-lognormal PSD can well represent aerosol size spectrum in most cases, future research efforts will include implementation for tri-modal aerosol mixtures in situations of cloud-formation or volcanic aerosols. Applying the algorithm to a suite of real cases over Beijing_RADI site, we found that our retrievals are overall consistent with AERONET inversion products, but can offer mode

  20. Dual-aureole and sun spectrometer system for airborne measurements of aerosol optical properties.

    PubMed

    Zieger, Paul; Ruhtz, Thomas; Preusker, Rene; Fischer, Jürgen

    2007-12-10

    We have designed an airborne spectrometer system for the simultaneous measurement of the direct sun irradiance and the aureole radiance in two different solid angles. The high-resolution spectral radiation measurements are used to derive vertical profiles of aerosol optical properties. Combined measurements in two solid angles provide better information about the aerosol type without additional and elaborate measuring geometries. It is even possible to discriminate between absorbing and nonabsorbing aerosol types. Furthermore, they allow to apply additional calibration methods and simplify the detection of contaminated data (e.g., by thin cirrus clouds). For the characterization of the detected aerosol type a new index is introduced that is the slope of the aerosol phase function in the forward scattering region. The instrumentation is a flexible modular setup, which has already been successfully applied in airborne and ground-based field campaigns. We describe the setup as well as the calibration of the instrument. In addition, example vertical profiles of aerosol optical properties--including the aureole measurements--are shown and discussed.

  1. 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.

  2. 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

  3. AeroCom INSITU Project: Comparison of Aerosol Optical Properties from In-situ Surface Measurements and Model Simulations

    NASA Astrophysics Data System (ADS)

    Schmeisser, L.; Andrews, E.; Schulz, M.; Fiebig, M.; Zhang, K.; Randles, C. A.; Myhre, G.; Chin, M.; Stier, P.; Takemura, T.; Krol, M. C.; Bian, H.; Skeie, R. B.; da Silva, A. M., Jr.; Kokkola, H.; Laakso, A.; Ghan, S.; Easter, R. C.

    2015-12-01

    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 have the unique property of being traceable to physical standards, which is a big asset in accomplishing the overarching goal of bettering the accuracy of aerosol processes and predicative capability of global climate models. The INSITU project looks at how well models reproduce aerosol climatologies on 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, using GOCART and other models participating in this AeroCom project, show substantial model biases in absorption and scattering coefficients compared to surface measurements, though the sign and magnitude of the bias varies with location and optical property. Spatial patterns in the biases highlight model weaknesses, e.g., the inability of models to properly simulate aerosol characteristics at sites with complex topography (see Figure 1). Additionally, differences in modeled and measured systematic variability of aerosol optical properties suggest that some models are not accurately capturing specific aerosol co-dependencies, for example, the tendency of in-situ surface single scattering albedo to decrease with decreasing aerosol extinction coefficient. This study elucidates specific problems with current aerosol models and suggests additional model runs and perturbations that could further evaluate the discrepancies between measured and modeled

  4. The Measurement of Aerosol Optical Properties using Continuous Wave Cavity Ring-Down Techniques

    NASA Technical Reports Server (NTRS)

    Strawa, Anthony W.; Castaneda, Rene; Owano, Thomas; Baer, Douglas S.; Paldus, Barbara A.; Gore, Warren J. (Technical Monitor)

    2002-01-01

    Large uncertainties in the effects that aerosols have on climate require improved in situ measurements of extinction coefficient and single-scattering albedo. This paper describes the use of continuous wave cavity ring-down (CW-CRD) technology to address this problem. The innovations in this instrument are the use of CW-CRD to measure aerosol extinction coefficient, the simultaneous measurement of scattering coefficient, and small size suitable for a wide range of aircraft applications. Our prototype instrument measures extinction and scattering coefficient at 690 nm and extinction coefficient at 1550 nm. The instrument itself is small (60 x 48 x 15 cm) and relatively insensitive to vibrations. The prototype instrument has been tested in our lab and used in the field. While improvements in performance are needed, the prototype has been shown to make accurate and sensitive measurements of extinction and scattering coefficients. Combining these two parameters, one can obtain the single-scattering albedo and absorption coefficient, both important aerosol properties. The use of two wavelengths also allows us to obtain a quantitative idea of the size of the aerosol through the Angstrom exponent. Minimum sensitivity of the prototype instrument is 1.5 x 10(exp -6)/m (1.5 M/m). Validation of the measurement of extinction coefficient has been accomplished by comparing the measurement of calibration spheres with Mie calculations. This instrument and its successors have potential to help reduce uncertainty currently associated with aerosol optical properties and their spatial and temporal variation. Possible applications include studies of visibility, climate forcing by aerosol, and the validation of aerosol retrieval schemes from satellite data.

  5. The Measurement of Aerosol Optical Properties Using Continuous Wave Cavity Ring-Down Techniques

    NASA Technical Reports Server (NTRS)

    Strawa, A. W.; Owano, T.; Castaneda, R.; Baer, D. S.; Paldus, B. A.; Gore, Warren J. (Technical Monitor)

    2002-01-01

    Large uncertainties in the effects that aerosols have on climate require improved in-situ measurements of extinction coefficient and single-scattering albedo. This abstract describes the use of continuous wave cavity ring-down (CW-CRD) technology to address this problem. The innovations in this instrument are the use of CW-CRD to measure aerosol extinction coefficient, the simultaneous measurement of scattering coefficient, and small size suitable for a wide range of aircraft applications. Our prototype instrument measures extinction and scattering coefficient at 690 nm and extinction coefficient at 1550 nm. The instrument itself is small (60 x 48 x 15 cm) and relatively insensitive to vibrations. The prototype instrument has been tested in our lab and used in the field. While improvements in performance are needed, the prototype has been shown to make accurate and sensitive measurements of extinction and scattering coefficients. Combining these two parameters, one can obtain the single-scattering albedo and absorption coefficient, both important aerosol properties. The use of two wavelengths also allows us to obtain a quantitative idea of the size of the aerosol through the Angstrom exponent. Minimum sensitivity of the prototype instrument is 1.5 x 10(exp -6)/m (1.5/Mm). Validation of the measurement of extinction coefficient has been accomplished by comparing the measurement of calibration spheres with Mie calculations. This instrument and its successors have potential to help reduce uncertainty currently associated with aerosol optical properties and their spatial and temporal variation. Possible applications include studies of visibility, climate forcing by aerosol, and the validation of aerosol retrieval schemes from satellite data.

  6. Aircraft measurements of aerosol properties during GoAmazon - G1 and HALO inter-comparison

    NASA Astrophysics Data System (ADS)

    Mei, F.; Cecchini, M. A.; Wang, J.; Tomlinson, J. M.; Comstock, J. M.; Hubbe, J. M.; Pekour, M. S.; Machado, L.; Wendisch, M.; Longo, K.; Martin, S. T.; Schmid, B.; Weinzierl, B.; Krüger, M. L.; Zöger, M.

    2015-12-01

    Currently, the indirect effects of atmospheric aerosols remain the most uncertain components in forcing of climate change over the industrial period (IPCC, 2013). This large uncertainty is partially a result of our incomplete understanding of the ability of particles to form cloud droplets under atmospherically relevant supersaturations. One objective of the US Department of Energy (DOE) Green Ocean Amazon Project (GoAmazon2014/5) is to understand the influence of the emission from Manaus, a tropical megacity, on aerosol size, concentration, and chemical composition, and their impact on cloud condensation nuclei (CCN) spectrum. The GoAmazon2014/5 study was an international campaign with the collaboration efforts from US, Brazil and Germany. During the intensive operation period, in the dry season (Sep. 1st - Oct. 10th, 2014), aerosol concentration, size distributions, and CCN spectra, both under pristine conditions and inside the Manaus plume, were characterized in-situ from the DOE Gulfstream-1 (G-1) research aircraft and German HALO aircraft during 4 coordinated flights on Sep. 9th, Sep. 16th, Sep 21st and Oct. 1st, 2014. During those four flights, aerosol number concentrations and CCN concentrations at two supersaturations (0.25% and 0.5%) were measured by condensation particle counters (CPCs) and a DMT dual column CCN counter onboard both G-1 and HALO. Aerosol size distribution was also measured by a Fast Integrated Mobility Spectrometer (FIMS) aboard the G-1 and is compared with the size distribution from Ultra High Sensitivity Aerosol Spectrometer - Airborne (UHSAS-A, DMT), which were deployed both on the G-1 and the HALO. Good agreement between the aerosol properties measured from the two aircraft has been achieved. The vertical profiles of aerosol size distribution and CCN spectrum will be discussed.

  7. Aerosol Properties over the Eastern North Pacific based on Measurements from the MAGIC Field Campaign

    NASA Astrophysics Data System (ADS)

    Lewis, E. R.; Senum, G.; Springston, S. R.; Kuang, C.

    2015-12-01

    The MAGIC field campaign, funded and operated by the ARM (Atmospheric Radiation Measurement) Climate Research Facility of the US Department of Energy, occurred between September 2012 and October, 2013 aboard the Horizon Lines cargo container ship Spirit making regular trips between Los Angeles, CA and Honolulu, HI. Along this route, which lies very near the GPCI (GCSS Pacific Cross-section Intercomparison) transect, the predominant cloud regime changes from stratocumulus near the California coast to trade-wind cumulus near Hawaii. The transition between these two regimes is poorly understood and not accurately represented in models. The goal of MAGIC was to acquire statistic of this transition and thus improve its representation in models by making repeated transects through this region and measuring properties of clouds and precipitation, aerosols, radiation, and atmospheric structure. To achieve these goals, the Second ARM Mobile Facility (AMF2) was deployed on the Horizon Spirit as it ran its regular route between Los Angeles and Honolulu. AMF2 consists of three 20-foot SeaTainers and includes three radars and other instruments to measure properties of clouds and precipitation; the Aerosol Observing System (AOS), which has a suite of instruments to measure properties of aerosols; and other instruments to measure radiation, meteorological quantities, and sea surface temperature. Two technicians accompanied the AMF2, and scientists rode the ship as observers. MAGIC made nearly 20 round trips between Los Angeles and Honolulu (and thus nearly 40 excursions through the stratocumulus-to-cumulus transition) and spent 200 days at sea, collecting an unprecedented data set. Aerosol properties measured with the AOS include number concentration and size distribution, CCN activity, hygroscopic growth, and light-scattering and absorption. Additionally, more than one hundred filter samples were collected. Aerosol properties and their spatial and temporal behavior are discussed

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

    SciTech Connect

    Torres, B.; Toledano, C.; Cachorro, V. E.; Bennouna, Y. S.; Fuertes, D.; Gonzalez, R.; Frutos, A. M. de; Berjon, A. J.; Dubovik, O.; Goloub, P.; Podvin, T.; Blarel, L.

    2013-05-10

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

  9. The analysis of in situ and retrieved aerosol properties measured during three airborne field campaigns

    NASA Astrophysics Data System (ADS)

    Corr, Chelsea A.

    Aerosols can directly influence climate, visibility, and photochemistry by scattering and absorbing solar radiation. Aerosol chemical and physical properties determine how efficiently a particle scatters and/or absorbs incoming short-wave solar radiation. Because many types of aerosol can act as nuclei for cloud droplets (CCN) and a smaller population of airborne particles facilitate ice crystal formation (IN), aerosols can also alter cloud-radiation interactions which have subsequent impacts on climate. Thus aerosol properties determine the magnitude and sign of both the direct and indirect impacts of aerosols on radiation-dependent Earth System processes. This dissertation will fill some gaps in our understanding of the role of aerosol properties on aerosol absorption and cloud formation. Specifically, the impact of aerosol oxidation on aerosol spectral (350nm < lambda< 500nm) absorption was examined for two biomass burning plumes intercepted by the NASA DC-S aircraft during the Arctic Research of the Composition of the Troposphere from Aircraft and Satellites (ARCTAS) mission in Spring and Summer 2008. Spectral aerosol single scattering albedo (SSA) retrieved using actinic flux measured aboard the NASA DC-8 was used to calculate the aerosol absorption Angstrom exponents (AAE) for a 6-day-old plume on April 17 th and a 3-hour old plume on June 29th. Higher AAE values for the April 17th plume (6.78+/-0.38) indicate absorption by aerosol was enhanced in the ultraviolet relative to the visible portion of the short-wave spectrum in the older plume compared to the fresher plume (AAE= 3.34 0.11). These differences were largely attributed to the greater oxidation of the organic aerosol in the April 17th plume which can arise either from the aging of primary organic aerosol or the formation of spectrally-absorbing secondary organic aerosol. The validity of the actinic flux retrievals used above were also evaluated in this work by the comparison of SSA retrieved using

  10. Long term measurements of aerosol optical properties at a primary forest site in Amazonia

    NASA Astrophysics Data System (ADS)

    Rizzo, L. V.; Artaxo, P.; Müller, T.; Wiedensohler, A.; Paixão, M.; Cirino, G. G.; Arana, A.; Swietlicki, E.; Roldin, P.; Fors, E. O.; Wiedemann, K. T.; Leal, L. S. M.; Kulmala, M.

    2013-03-01

    A long term experiment was conducted in a primary forest area in Amazonia, with continuous in-situ measurements of aerosol optical properties between February 2008 and April 2011, comprising, to our knowledge, the longest database ever in the Amazon Basin. Two major classes of aerosol particles, with significantly different optical properties were identified: coarse mode predominant biogenic aerosols in the wet season (January-June), naturally released by the forest metabolism, and fine mode dominated biomass burning aerosols in the dry season (July-December), transported from regional fires. Dry particle median scattering coefficients at the wavelength of 550 nm increased from 6.3 Mm-1 to 22 Mm-1, whereas absorption at 637 nm increased from 0.5 Mm-1 to 2.8 Mm-1 from wet to dry season. Most of the scattering in the dry season was attributed to the predominance of fine mode (PM2) particles (40-80% of PM10 mass), while the enhanced absorption coefficients are attributed to the presence of light absorbing aerosols from biomass burning. As both scattering and absorption increased in the dry season, the single scattering albedo (SSA) did not show a significant seasonal variability, in average 0.86 ± 0.08 at 637 nm for dry aerosols. Measured particle optical properties were used to estimate the aerosol forcing efficiency at the top of the atmosphere. Results indicate that in this primary forest site the radiative balance was dominated by the cloud cover, particularly in the wet season. Due to the high cloud fractions, the aerosol forcing efficiency absolute values were below -3.5 W m-2 in 70% of the wet season days and in 46% of the dry season days. Besides the seasonal variation, the influence of out-of-Basin aerosol sources was observed occasionally. Periods of influence of the Manaus urban plume were detected, characterized by a consistent increase on particle scattering (factor 2.5) and absorption coefficients (factor 5). Episodes of biomass burning and mineral dust

  11. Long term measurements of aerosol optical properties at a pristine forest site in Amazonia

    NASA Astrophysics Data System (ADS)

    Rizzo, L. V.; Artaxo, P.; Müller, T.; Wiedensohler, A.; Paixão, M.; Cirino, G. G.; Arana, A.; Swietlicki, E.; Roldin, P.; Fors, E. O.; Wiedemann, K. T.; Leal, L. S. M.; Kulmala, M.

    2012-09-01

    A long term experiment was conducted in a pristine area in the Amazon forest, with continuous in situ measurements of aerosol optical properties between February 2008 and April 2011, comprising, to our knowledge, the longest database ever in Amazonia. Two types of aerosol particles, with significantly different optical properties were identified: coarse mode predominant biogenic aerosols in the wet season (January-June), naturally released by the forest metabolism, and fine mode dominated biomass burning aerosols in the dry season (July-December), transported from regional fires. Dry particle median scattering coefficients at the wavelength of 550 nm increased from 6.3 Mm-1 to 22 Mm-1, whereas absorption at 637 nm increased from 0.5 Mm-1 to 2.8 Mm-1 from wet to dry season. Most of the scattering in the dry season was attributed to the predominance of fine mode particles (40-80% of PM10 mass), while the enhanced absorption coefficients are attributed to the presence of light absorbing aerosols from biomass burning. As both scattering and absorption increased in the dry season, the single scattering albedo (SSA) did not show a significant seasonal variability, in average 0.86 ± 0.08 at 637 nm for dry particles. Measured particle optical properties were used to estimate the aerosol forcing efficiency at the top of the atmosphere. Results indicate that in this pristine forest site the radiative balance was dominated by the cloud cover, or, in other words, the aerosol indirect effect predominated over the direct effect, particularly in the wet season. Due to the high cloud fractions, the aerosol forcing efficiency was below -3.5 W m-2 in 70% of the wet season days and in 46% of the dry season days. These values are lower than the ones reported in the literature, which are based on remote sensing data. Besides the seasonal variation, the influence of external aerosol sources was observed occasionally. Periods of influence of the Manaus urban plume were detected

  12. Aerosol Properties over Southeastern China from Multi-Wavelength Raman and Depolarization Lidar Measurements

    NASA Astrophysics Data System (ADS)

    Heese, Birgit; Althausen, Dietrich; Baars, Holger; Bohlmann, Stephanie; Deng, Ruru

    2016-06-01

    A dataset of particle optical properties of highly polluted urban aerosol over the Pearl River Delta, Guangzhou, China is presented. The data were derived from multi-wavelengths Raman and depolarization lidar PollyXT and AERONET sun photometer measurements. The measurement campaign was conducted from Nov 2011 to June 2012. High aerosol optical depth was observed in the polluted atmosphere over this megacity, with a mean value of 0.54 ± 0.33 and a peak value of even 1.9. For the particle characterization the lidar ratio and the linear particle depolarization ratio, both at 532 nm, were used. The mean values of these properties are 48.0 sr ± 10.7 sr for the lidar ratio and 4%+-4% for the particle depolarization ratio, which means most depolarization measurements stayed below 10%. So far, most of these results indicate urban pollution particles mixed with particles arisen from biomass and industrial burning.

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

    DOE PAGES

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

    2013-01-01

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

  14. Airborne Sunphotometer Studies of Aerosol Properties and Effects, Including Closure Among Satellite, Suborbital Remote, and In situ Measurements

    NASA Technical Reports Server (NTRS)

    Russlee, Philip B.; Schmid, B.; Redemann, J.; Livingston, J. M.; Bergstrom, R. W.; Ramirez, S. A.; Hipskind, R. Stephen (Technical Monitor)

    2001-01-01

    Airborne sunphotometry has been used to measure aerosols from North America, Europe, and Africa in coordination with satellite and in situ measurements in TARFOX (1996), ACE-2 (1997), PRIDE (2000), and SAFARI 2000. Similar coordinated measurements of Asian aerosols are being conducted this spring in ACE-Asia and are planned for North American aerosols this summer in CLAMS. This paper summarizes the approaches used, key results, and implications for aerosol properties and effects, such as single scattering albedo and regional radiative forcing. The approaches exploit the three-dimensional mobility of airborne sunphotometry to access satellite scenes over diverse surfaces (including open ocean with and without sunglint) and to match exactly the atmospheric layers sampled by airborne in situ measurements and other radiometers. These measurements permit tests of the consistency, or closure, among such diverse measurements as aerosol size-resolved chemical composition; number or mass concentration; light extinction, absorption, and scattering (total, hemispheric back and 180 deg.); and radiative fluxes. In this way the airborne sunphotometer measurements provide a key link between satellite and in situ measurements that helps to understand any discrepancies that are found. These comparisons have led to several characteristic results. Typically these include: (1) Better agreement among different types of remote measurements than between remote and in situ measurements. (2) More extinction derived from transmission measurements than from in situ measurements. (3) Larger aerosol absorption inferred from flux radiometry than from in situ measurements. Aerosol intensive properties derived from these closure studies have been combined with satellite-retrieved fields of optical depth to produce fields of regional radiative forcing. We show results for the North Atlantic derived from AVHRR optical depths and aerosol intensive properties from TARFOX and ACE-2. Companion papers

  15. Aerosol Optical Properties and Chemical Composition Measured on the Ronald H. Brown During ACE-Asia

    NASA Astrophysics Data System (ADS)

    Quinn, P. K.; Bates, T. S.; Miller, T. L.; Coffman, D.

    2001-12-01

    Measurements of aerosol chemical, physical, and optical properties were made onboard the NOAA R/V Ronald H. Brown during the ACE-Asia Intensive Field Program to characterize Asian aerosol as it was transported across the Pacific Ocean. The ship traveled across the Pacific from Hawaii to Japan and into the East China Sea and the Sea of Japan. Trajectories indicate that remote marine air masses were sampled on the transit to Japan. In the ACE-Asia study region air masses from Japan, China, Mongolia, and the Korea Peninsula were sampled. A variety of aerosol types were encountered including those of marine, volcanic, crustal, and industrial origin. Presented here, for the different air masses encountered, are aerosol optical properties (scattering and absorption coefficients, single scattering albedo, Angstrom Exponent, and aerosol optical depth) and chemical composition (major ions, total organic and black carbon, and trace elements). Scattering by submicron aerosol (55 % RH and 550 nm) was less than 20 1/Mm during the transit from Hawaii to Japan. In continental air masses, values ranged from 60 to 320 1/Mm with the highest submicron scattering coefficients occurring during prefrontal conditions with a low marine boundary layer height and trajectories from Japan. For the continental air masses, the ratio of scattering by submicron to sub-10 micron aerosol during polluted conditions averaged 0.8 and during a dust event 0.41. Aerosol optical depth (500 nm) ranged from 0.08 during the Pacific transit to 1.3 in the prefrontal conditions described above. Optical depths during dust events ranged from 0.2 to 0.6. Submicron non-sea salt (nss) sulfate concentrations ranged from 0.5 ug/m-3 during the Pacific transit to near 30 ug/m-3 during the prefrontal conditions described above. Black carbon to total carbon mass ratios in air masses from Asia averaged 0.18 with highest values (0.32) corresponding to trajectories crossing the Yangtze River valley.

  16. Evolution of biomass burning aerosol over the Amazon: airborne measurements of aerosol chemical composition, microphysical properties, mixing state and optical properties during SAMBBA

    NASA Astrophysics Data System (ADS)

    Morgan, W.; Allan, J. D.; Flynn, M.; Darbyshire, E.; Hodgson, A.; Liu, D.; O'Shea, S.; Bauguitte, S.; Szpek, K.; Johnson, B.; Haywood, J.; Longo, K.; Artaxo, P.; Coe, H.

    2013-12-01

    Biomass burning represents one of the largest sources of particulate matter to the atmosphere, resulting in a significant perturbation to the Earth's radiative balance coupled with serious impacts on public health. On regional scales, the impacts are substantial, particularly in areas such as the Amazon Basin where large, intense and frequent burning occurs on an annual basis for several months. Absorption by atmospheric aerosols is underestimated by models over South America, which points to significant uncertainties relating to Black Carbon (BC) aerosol properties. Initial results from the South American Biomass Burning Analysis (SAMBBA) field experiment, which took place during September and October 2012 over Brazil on-board the UK Facility for Airborne Atmospheric Measurement (FAAM) BAe-146 research aircraft, are presented here. Aerosol chemical composition was measured by an Aerodyne Aerosol Mass Spectrometer (AMS) and a DMT Single Particle Soot Photometer (SP2). The physical, chemical and optical properties of the aerosols across the region will be characterized in order to establish the impact of biomass burning on regional air quality, weather and climate. The aircraft sampled a range of conditions including sampling of pristine Rainforest, fresh biomass burning plumes, regional haze and elevated biomass burning layers within the free troposphere. The aircraft sampled biomass burning aerosol across the southern Amazon in the states of Rondonia and Mato Grosso, as well as in a Cerrado (Savannah-like) region in Tocantins state. This presented a range of fire conditions, in terms of their number, intensity, vegetation-type and their combustion efficiencies. Near-source sampling of fires in Rainforest environments suggested that smouldering combustion dominated, while flaming combustion dominated in the Cerrado. This led to significant differences in aerosol chemical composition, particularly in terms of the BC content, with BC being enhanced in the Cerrado

  17. The unique properties of agricultural aerosols measured at a cattle feeding operation

    NASA Astrophysics Data System (ADS)

    Hiranuma, N.; Brooks, S. D.; Gramann, J.; Auvermann, B. W.

    2011-05-01

    Housing roughly 10 million head of cattle in the United States alone, open air cattle feedlots represent a significant but poorly constrained source of atmospheric particles. Here we present a comprehensive characterization of physical and chemical properties of particles emitted from a large representative cattle feedlot in the Southwest United States. In the summer of 2008, measurements and samplings were conducted at the nominally upwind and downwind edges of the facility. A series of far-field measurements and samplings was also conducted 3.5 km north of the facility. Two instruments, a GRIMM Sequential Mobility Particle Sizer (SMPS) and a GRIMM Portable Aerosol Spectrometer (PAS), were used to measure particle size distributions over the range of 0.01 to 25 μm diameter. Raman microspectroscopy (RM) was used to determine the chemical composition of particles on a single particle basis. Volume size distributions of fugitive dust were dominated by coarse mode particles. Twenty-four hour averaged concentrations of PM10 (particulate matter with a diameter of 10 μm or less) were as high as 1200 μg m-3 during the campaign. The primary constituents of the particulate matter were carbonaceous materials, such as humic acid, water soluble organics, and less soluble fatty acids, including stearic acid and tristearin. A significant percentage of the organic particles, up to 28 %, were composed of internally mixed with salts. Basic characteristics such as size distribution and composition of agricultural aerosols were found to be different than the properties of those found in urban and semi-urban aerosols. Failing to account for such differences will lead to serious errors in estimates of aerosol effects on climate, visibility, and public health.

  18. The Unique Properties of Agricultural Aerosols Measured at a Cattle Feeding Operation

    SciTech Connect

    Hiranuma, Naruki; Brooks, S. D.; Gramann, J.; Auvermann, B. W.

    2011-05-11

    Housing roughly 10 million head of cattle in the United States alone, open air cattle feedlots represent a significant but poorly constrained source of atmospheric particles. Here we present a comprehensive characterization of physical and chemical properties of particles emitted from a large representative cattle feedlot in the Southwest United States. In the summer of 2008, measurements and samplings were conducted at the nominally upwind and downwind edges of the facility. A series of far-field measurements and samplings was also conducted 3.5 km north of the facility. Two instruments, a GRIMM Sequential Mobility Particle Sizer (SMPS) and a GRIMM Portable Aerosol Spectrometer (PAS), were used to measure particle size distributions over the range of 0.01 to 25 μm diameter. Raman microspectroscopy (RM) was used to determine the chemical composition of particles on a single particle basis. Volume size distributions of fugitive dust were dominated by coarse mode particles. Twenty-four hour averaged concentrations of PM10 (particulate matter with a diameter of 10 µm or less) were as high as 1200 μg/m3 during the campaign. The primary constituents of the particulate matter were carbonaceous materials, such as humic acid, water soluble organics, and less soluble fatty acids, including stearic acid and tristearin. A significant fraction of the organic particles was composed of internally mixed with salts. Basic characteristics such as size distribution and composition of agricultural aerosols were found to be different than the properties of those found in urban and semi-urban aerosols. Failing to account for such differences will lead to serious errors in estimates of aerosol effects on climate, visibility, and public health.

  19. Long term measurements of atmospheric aerosol optical properties in the Eastern Mediterranean

    NASA Astrophysics Data System (ADS)

    Kalivitis, N.; Bougiatioti, A.; Kouvarakis, G.; Mihalopoulos, N.

    2011-11-01

    Optical properties of atmospheric aerosol particles have been recorded at a remote location of the Eastern Mediterranean on a continuous basis since 2000. Measurements of aerosol scattering coefficient (bsp) and absorption coefficient (bap) have been conducted, providing the longest data series of such ground based measurements in the Eastern Mediterranean basin. bsp shows an annual cycle with maximum values observed during summer and minimum during winter. In addition, in periods when mineral dust is transported into the area, high values are observed. It has been shown that both the level and the annual variation of bsp can be well represented if ammonium sulfate (AS) and particulate organic matter (POM) are assumed as the only scattering species in the aerosol phase. bap was measured at three wavelengths using two different instruments and a single wavelength data series was extracted. Maximum values of bap were observed during summer and during periods with extended dust transport to the area. If mineral dust particles are present in the atmosphere they can contribute up to 80% of bap levels at the visible wavelengths.

  20. Airborne High Spectral Resolution Lidar Measurements of Aerosol Distributions and Properties during the NASA DISCOVER-AQ Missions

    NASA Astrophysics Data System (ADS)

    Ferrare, R. A.; Hostetler, C. A.; Hair, J. W.; Scarino, A. J.; Burton, S. P.; Harper, D. B.; Cook, A. L.; Berkoff, T.; Rogers, R. R.; Seaman, S. T.; Fenn, M. A.; Sawamura, P.; Clayton, M.; Mueller, D.; Chemyakin, E.; Anderson, B. E.; Beyersdorf, A. J.; Ziemba, L. D.; Crawford, J. H.

    2015-12-01

    The NASA Langley Research Center airborne High Spectral Resolution Lidars, HSRL-1 and HSRL-2, were deployed for the DISCOVER-AQ (Deriving Information on Surface Conditions from COlumn and VERtically Resolved Observations Relevant to Air Quality) missions. DISCOVER-AQ provided systematic and concurrent observations of column-integrated, surface, and vertically-resolved distributions of aerosols and trace gases to improve the interpretation of satellite observations related to air quality. HSRL-1, deployed during the first DISCOVER-AQ mission over the Washington DC-Baltimore region, measured profiles of aerosol backscatter and depolarization (532, 1064 nm) and aerosol extinction and optical thickness (AOT) (532 nm). HSRL-2, the first airborne multiwavelength HSRL, was deployed for the following three DISCOVER-AQ missions over the California Central Valley, Houston, and Denver. HSRL-2 measures profiles of aerosol backscatter and depolarization (355, 532, 1064 nm) and aerosol extinction and AOT (355, 532 nm). Additional HSRL-2 data products include aerosol type, mixed layer depth, and range-resolved aerosol microphysical parameters. The HSRL measurements reveal the temporal, spatial, and vertical variability of aerosol optical properties over these locations. HSRL measurements show that surface PM2.5 concentrations were better correlated with near surface aerosol extinction than AOT scaled by the mixed layer height. During the missions over Washington DC-Baltimore, Houston, and Denver, only about 20-65% of AOT was within the mixed layer. In contrast, nearly all of the AOT was within the mixed layer over the California Central Valley. HSRL-2 retrievals of aerosol fine mode volume concentration and effective radius compare well with coincident airborne in situ measurements and vary with relative humidity. HSRL-2 retrievals of aerosol fine mode volume concentration were also used to derive PM2.5 concentrations which compare well with surface PM2.5 measurements.

  1. Regional aerosol properties: Comparisons of boundary layer measurements from ACE 1, ACE 2, Aerosols99, INDOEX, ACE Asia, TARFOX, and NEAQS

    NASA Astrophysics Data System (ADS)

    Quinn, Patricia K.; Bates, Timothy S.

    2005-07-01

    Means and variability of aerosol chemical composition and optical properties are compared for the first and second Aerosol Characterization Experiments (ACE 1 and ACE 2), a cruise across the Atlantic (Aerosols99), the Indian Ocean Experiment (INDOEX), the Asian Aerosol Characterization Experiment (ACE Asia), the Tropospheric Aerosol Radiative Forcing Observational Experiment (TARFOX), and the New England Air Quality Study (NEAQS). These experiments were focused either on the remote marine atmosphere (ACE 1) or areas downwind of continental aerosol source regions including western Europe, North America, Africa, India, and Asia. Presented here are size-segregated concentrations of aerosol mass, sea salt, non-sea-salt (nss) SO4=, NH4+, NO3-, dust, organic carbon (OC), elemental carbon (EC), and nss K+, as well as mass ratios that are commonly used to identify aerosol sources and to assess aerosol processing (Cl- to Na+, OC to nss SO4=, EC to total carbon (TC), EC to nss SO4=, nss K+ to EC, Fe to Al, and Si to Al). Optical properties that are compared include size-segregated scattering, backscattering, and absorption coefficients, and single-scattering albedo at 550 nm. Size-segregated mass scattering and mass absorption efficiencies for the total aerosol and mass extinction efficiencies for the dominant chemical components also are compared. In addition, we present the contribution to light extinction by the dominant chemical components for each region. All data are based on shipboard measurements performed at a relative humidity of 55 ± 5%. Scattering coefficients and single-scattering albedos also are reported at ambient relative humidity (RH) using published values of f(RH). Finally, aerosol optical depths from each region are compared. Identical sampling protocols were used in all experiments in order to eliminate sampling biases and to make the data directly comparable. Major findings include (1) nss SO4= makes up only 16 to 46% of the submicron aerosol mass

  2. Aerosol Properties under Air Quality Control Measures of APEC 2014 in Beijing

    NASA Astrophysics Data System (ADS)

    Chen, X.; Xu, H.; Lv, Y.; Xie, Y.; Li, K.; Li, Z.; Li, D.; Ma, Y.; Mei, X.

    2015-12-01

    Because the economic and society were developing fast in the middle of last century, Los Angeles and London both were polluted by photochemical smog, which massacred thousands of people. Now, many regions are often covered by heavy haze in those large developing countries, especially in China and India. The Asia-Pacific Economic Cooperation (APEC) was held in Beijing during 5-11 November 2014. Beijing, Hebei, Tianjin, Shandong, Shanxi, Inner Mongolia reduced air pollution emissions for the APEC 2014 meeting held in Beijing. Only in Hebei province, there were 1028 factories stopped or restricted and 881 construction sites stopped. Half of the cars were prohibited driving even in the Zibo city which is 400 km far from Beijing. For scientific aims, these control measures were indeed a huge and uncommon atmospheric experiment led by the government. During the experiment, what did the "APEC Blue" mean? We analyzed aerosol properties with the data of an AERONET site in Beijing which is located 500m far from the main reception hall of APEC 2014. The Cimel solar photometers can give a series parameters of aerosol and water vapor. In this paper, we used CE318 solar photometer which is the main instrument of NASA AERONET. The CE318 of RADI belongs to the Chinese SONET (Sun-sky radiometer Observation NETwork) too. We analyzed the total, coarse and fine Aerosol Optical Depth (AOD), Fine-Mode Fraction (FMF) and Ångström exponent, Size Distribution and Real Refractive Index. In conclusion, the aerosol properties were analysed with the measurements of a sun photometer. During the APEC 2014, AOD decreased obviously with a 0.27 mean value compared with the annual mean 0.7. Around Beijing, the southern is polluted emission area including the cross part of Shandong, Shanxi, Hebei, Henan four provinces, and the northern is clean for less fine mode particles emission in the large Inner Mongolia province. In fact, during the APEC 2014, the weather condition was not good for the

  3. Contribution of long-range transported aerosols to aerosol optical and physical properties: 3-year measurements at Gosan, Korea

    NASA Astrophysics Data System (ADS)

    Heo, J.; Kim, S. W.; Kim, J. H.; Ogren, J. A.; Yoon, S. C.

    2015-12-01

    Recently, more attentions have been paid to air quality in East Asia due to the enhanced loading of atmospheric pollutants related to rapid industrialization. Gosan Climate Observatory (GCO), Korea is regarded as an ideal site to study the transport of atmospheric pollutants because it is frequently influenced by various airmasses from China, Korea, Japan and Pacific Ocean. In order to understand aerosol optical and physical properties according to airmass transport routes, three-year (2012-2014) continuous measurements of aerosol scattering/absorption coefficient and number size distribution were analyzed, together with 48-hour backward trajectory calculations. The averaged aerosol absorption (σa) and scattering coefficient (σs) for airmasses transported from North China (NC; 36% of all trajectories) were 6.65 Mm-1 and 94.72 Mm-1 at 550 nm wavelength, respectively, which were similar to those for stagnant airmasses (ST; 22% of all trajectories; σa: 6.26 Mm-1, σs: 93.99 Mm-1). The highest values of σa (7.03 Mm-1) and σs (108.34 Mm-1) were observed when airmasses were traveled from South China (SC; 11% of all trajectories). σa and σs for airmasses from Korean Peninsula (KP; 7% of all trajectories) and Pacific Ocean (PO; 14% of all trajectories; in parenthesis) were 5.63 (2.76) Mm-1 and 73.63 (50.93) Mm-1, respectively. Compared to other airmasses, the higher values of Scattering Angstrom Exponent (SAE) for ST (1.65) is thought to be the build-up of anthropogenic fine particulate pollutants. The Absorption Angstrom Exponent (AAE) was estimated to be 1.32 for NC airmass and 1.02 for SC airmass. Over the study period, 130 days of total 557 days were identified as new particle formation and growth event (NPF) from Scanning Mobility Particle Sizer (SMPS) measurements by Cyclostationary Empirical Orthogonal Function (CSEOF) approach. Especially, 55.4% (72 days) of total 130 NPF days were found when a cold and dry airmass comes from NC after passing the frontal

  4. Ground-based SMART-COMMIT Measurements for Studying Aerosol and Cloud Properties

    NASA Technical Reports Server (NTRS)

    Tsay, Si-Chee

    2008-01-01

    From radiometric principles, it is expected that the retrieved properties of extensive aerosols and clouds from reflected/emitted measurements by satellite (and/or aircraft) should be consistent with those retrieved from transmitted/emitted radiance observed at the surface. Although space-borne remote sensing observations cover large spatial domain, they are often plagued by contamination of surface signatures. Thus, ground-based in-situ and remote-sensing measurements, where signals come directly from atmospheric constituents, the sun, and/or the Earth-atmosphere interactions, provide additional information content for comparisons that confirm quantitatively the usefulness of the integrated surface, aircraft, and satellite data sets. The development and deployment of SMARTCOMMIT (Surface-sensing Measurements for Atmospheric Radiative Transfer - Chemical, Optical & Microphysical Measurements of In-situ Troposphere) mobile facilities are aimed for the optimal utilization of collocated ground-based observations as constraints to yield higher fidelity satellite retrievals and to determine any sampling bias due to target conditions. To quantify the energetics of the surface-atmosphere system and the atmospheric processes, SMART-COMMIT instruments fall into three categories: flux radiometer, radiance sensor and in-situ probe. In this paper, we will demonstrate the capability of SMART-COMMIT in recent field campaigns (e.g., CRYSTAL-FACE, UAE 2, BASEASIA, NAMMA) that were designed and executed to study the compelling variability in temporal scale of both anthropogenic and natural aerosols (e.g., biomass-burning smoke, airborne dust) and cirrus clouds. We envision robust approaches in which well-collocated ground-based measurements and space-borne observations will greatly advance our knowledge of extensive aerosols and clouds.

  5. Continuous and automatic measurement of atmospheric structures and aerosols optical properties with R-Man510 nitrogen Raman lidar

    NASA Astrophysics Data System (ADS)

    Royer, P.; Renaudier, M.; Sauvage, L.; Boquet, M.; Thobois, L.; Bizard, A.

    2012-04-01

    A new compact and light nitrogen Raman lidar (R-Man510) has recently been developed by Leosphere company. This UV-lidar system is based on a low energy diode pumped Nd:YAG laser at 355 nm and has been developed to be operated unmanly for the meteorological and airport needs. Measurements are typically performed with a vertical resolution between 15 and 60 m and a temporal resolution between 30 seconds (for elastic channel) and 10 minutes (for Raman channel). The elastic channel of the lidar is used to automatically detect up to 9 atmospheric structures (Plantery Boundary Layer height, aerosol and cloud layers) in quasi real-time. Aerosols are classified in 6 types (pollution aerosols, desert dusts, volcanic ashes, marine aerosols, biomass burning and no aerosols) considering informations on depolarization ratio determined with the two cross-polarized elastic channels and on aerosols optical properties (extinction-to-backscatter ratio, aerosol backscatter and extinction coefficients) determined thanks to the nitrogen Raman channel at 387 nm. Aerosols optical properties can then been used for the assessment of mass concentrations which is crucial in case of hypothetical volcanic eruption. We will present the first results obtained with this new commercial lidar system. Daytime and nighttime performances of the system will be analyzed and compared with simulations from an instrumental model.

  6. Simultaneous retrieval of aerosol and surface optical properties from combined airborne- and ground-based direct and diffuse radiometric measurements

    NASA Astrophysics Data System (ADS)

    Gatebe, C. K.; Dubovik, O.; King, M. D.; Sinyuk, A.

    2009-12-01

    This paper presents a new method for simultaneously retrieving aerosol and surface reflectance properties from combined airborne and ground-based direct and diffuse radiometric measurements. The method is based on the standard Aerosol Robotic Network (AERONET) method for retrieving aerosol size distribution, complex index of refraction, and single scattering albedo, but modified to retrieve aerosol properties in two layers, below and above the aircraft, and parameters on surface optical properties from combined datasets (Cloud Absorption Radiometer, CAR, and AERONET data). A key advantage of this method is the inversion of all available spectral and angular data at the same time, while accounting for the influence of noise in the inversion procedure using statistical optimization. The wide spectral (0.34-2.30 μm) and angular range (180°) of the CAR instrument, combined with observations from an AERONET sunphotometer, provide sufficient measurement constraints for characterizing aerosol and surface properties with minimal assumptions. The robustness of the method was tested on observations made during four different field campaigns: (a) the Southern African Regional Science Initiative 2000 over Mongu, Zambia, (b) the Intercontinental Transport Experiment-Phase B over Mexico City, Mexico (c) Cloud and Land Surface Interaction Campaign over the Atmospheric Radiation Measurement (ARM) Central Facility, Oklahoma, USA, and (d) the Arctic Research of the Composition of the Troposphere from Aircraft and Satellites (ARCTAS) over Elson Lagoon in Barrow, Alaska, USA. The four areas are dominated by different surface characteristics and aerosol types, and therefore provide good test cases for the new inversion method.

  7. Simultaneous Retrieval of Aerosol and Surface Optical Properties from Combined Airborne- and Ground-Based Direct and Diffuse Radiometric Measurements

    NASA Technical Reports Server (NTRS)

    Gatebe, C. K.; Dubovik, O.; King, M. D.; Sinyuk, A.

    2010-01-01

    This paper presents a new method for simultaneously retrieving aerosol and surface reflectance properties from combined airborne and ground-based direct and diffuse radiometric measurements. The method is based on the standard Aerosol Robotic Network (AERONET) method for retrieving aerosol size distribution, complex index of refraction, and single scattering albedo, but modified to retrieve aerosol properties in two layers, below and above the aircraft, and parameters on surface optical properties from combined datasets (Cloud Absorption Radiometer (CAR) and AERONET data). A key advantage of this method is the inversion of all available spectral and angular data at the same time, while accounting for the influence of noise in the inversion procedure using statistical optimization. The wide spectral (0.34-2.30 m) and angular range (180 ) of the CAR instrument, combined with observations from an AERONET sunphotometer, provide sufficient measurement constraints for characterizing aerosol and surface properties with minimal assumptions. The robustness of the method was tested on observations made during four different field campaigns: (a) the Southern African Regional Science Initiative 2000 over Mongu, Zambia, (b) the Intercontinental Transport Experiment-Phase B over Mexico City, Mexico (c) Cloud and Land Surface Interaction Campaign over the Atmospheric Radiation Measurement (ARM) Central Facility, Oklahoma, USA, and (d) the Arctic Research of the Composition of the Troposphere from Aircraft and Satellites (ARCTAS) over Elson Lagoon in Barrow, Alaska, USA. The four areas are dominated by different surface characteristics and aerosol types, and therefore provide good test cases for the new inversion method.

  8. Measurements of the chemical, physical, and optical properties of single aerosol particles

    NASA Astrophysics Data System (ADS)

    Moffet, Ryan Christopher

    Knowledge of aerosol physical, chemical, optical properties is essential for judging the effect that particulates have on human health, climate and visibility. The aerosol time-of-flight mass spectrometer (ATOFMS) is capable of measuring, in real-time, the size and chemical composition of atmospheric aerosols. This was exemplified by the recent deployments of the ATOFMS to Mexico City and Riverside. The ATOFMS provided rapid information about the major particle types present in the atmosphere. Industrial sources of particles, such as fine mode particles containing lead, zinc and chloride were detected in Mexico City. The rapid time response of the ATOFMS was also exploited to characterize a coarse particle concentrator used in human health effects studies. The ATOFMS showed the ability to detect changes in particle composition with a time resolution of 15 min during short 2 hour human exposure studies. As a major component of this work, an optical measurement has been added to the ATOFMS. The scattered light intensity was acquired for each sized and chemically analyzed particle. This scattering information together with the particle aerodynamic diameter, enabled the refractive index and density of the aerosol to be retrieved. This method was validated in the laboratory using different test particles such as oils, aqueous salt solutions and black carbon particles. It was found that the nozzle-type inlet does not evaporate aqueous salt particles as has been observed for aerodynamic lens inlets. These new optical and microphysical measurements were integrated into the ATOFMS for field deployment in Riverside and Mexico City. For both cities, the different mixing states were found to have unique refractive indexes and densities. A fraction of the strongly absorbing elemental carbon particles were observed to have a spherical morphology due to heavy mixing with secondary species. In addition to the quantitative refractive index and effective density measurements

  9. Vertical profiles of aerosol optical properties and the solar heating rate estimated by combining sky radiometer and lidar measurements

    NASA Astrophysics Data System (ADS)

    Kudo, Rei; Nishizawa, Tomoaki; Aoyagi, Toshinori

    2016-07-01

    The SKYLIDAR algorithm was developed to estimate vertical profiles of aerosol optical properties from sky radiometer (SKYNET) and lidar (AD-Net) measurements. The solar heating rate was also estimated from the SKYLIDAR retrievals. The algorithm consists of two retrieval steps: (1) columnar properties are retrieved from the sky radiometer measurements and the vertically mean depolarization ratio obtained from the lidar measurements and (2) vertical profiles are retrieved from the lidar measurements and the results of the first step. The derived parameters are the vertical profiles of the size distribution, refractive index (real and imaginary parts), extinction coefficient, single-scattering albedo, and asymmetry factor. Sensitivity tests were conducted by applying the SKYLIDAR algorithm to the simulated sky radiometer and lidar data for vertical profiles of three different aerosols, continental average, transported dust, and pollution aerosols. The vertical profiles of the size distribution, extinction coefficient, and asymmetry factor were well estimated in all cases. The vertical profiles of the refractive index and single-scattering albedo of transported dust, but not those of transported pollution aerosol, were well estimated. To demonstrate the performance and validity of the SKYLIDAR algorithm, we applied the SKYLIDAR algorithm to the actual measurements at Tsukuba, Japan. The detailed vertical structures of the aerosol optical properties and solar heating rate of transported dust and smoke were investigated. Examination of the relationship between the solar heating rate and the aerosol optical properties showed that the vertical profile of the asymmetry factor played an important role in creating vertical variation in the solar heating rate. We then compared the columnar optical properties retrieved with the SKYLIDAR algorithm to those produced with the more established scheme SKYRAD.PACK, and the surface solar irradiance calculated from the SKYLIDAR

  10. Comparison of the aerosol optical properties and size distribution retrieved by sun photometer with in situ measurements at midlatitude

    NASA Astrophysics Data System (ADS)

    Chauvigné, Aurélien; Sellegri, Karine; Hervo, Maxime; Montoux, Nadège; Freville, Patrick; Goloub, Philippe

    2016-09-01

    Aerosols influence the Earth radiative budget through scattering and absorption of solar radiation. Several methods are used to investigate aerosol properties and thus quantify their direct and indirect impacts on climate. At the Puy de Dôme station, continuous high-altitude near-surface in situ measurements and low-altitude ground-based remote sensing atmospheric column measurements give the opportunity to compare the aerosol extinction measured with both methods over a 1-year period. To our knowledge, it is the first time that such a comparison is realised with continuous measurements of a high-altitude site during a long-term period. This comparison addresses to which extent near-surface in situ measurements are representative of the whole atmospheric column, the aerosol mixing layer (ML) or the free troposphere (FT). In particular, the impact of multi-aerosol layers events detected using lidar backscatter profiles is analysed. A good correlation between in situ aerosol extinction coefficient and aerosol optical depth (AOD) measured by the Aerosol Robotic Network (AERONET) sun photometer is observed with a correlation coefficient around 0.80, indicating that the in situ measurements station is representative of the overall atmospheric column. After filtering for multilayer cases and correcting for each layer optical contribution (ML and FT), the atmospheric structure seems to be the main factor influencing the comparison between the two measurement techniques. When the site lies in the ML, the in situ extinction represents 45 % of the sun photometer ML extinction while when the site lies within the FT, the in situ extinction is more than 2 times higher than the FT sun photometer extinction. Moreover, the assumption of a decreasing linear vertical aerosol profile in the whole atmosphere has been tested, significantly improving the instrumental agreement. Remote sensing retrievals of the aerosol particle size distributions (PSDs) from the sun photometer

  11. Intercomparison of Aerosol Optical Properties Derived from PREDE Skyradiometer and CIMEL Sunphotometer Measurements for the DRAGON-Korea Campaign

    NASA Astrophysics Data System (ADS)

    Choi, Y.; Ghim, Y.; Holben, B. N.

    2012-12-01

    The Distributed Regional Aerosol Gridded Observation Networks (DRAGON) campaign for validation of satellite aerosol products and comparison/validation of ground-based aerosol retrievals has been launched in Asia. It was conducted in Korea (DRAGON-Korea) between March and May 2012, with CIMEL sunphotometers being operated at around 20 sites throughout the country. The Hankuk University of Foreign Studies site (Hankuk_UFS, 37.02oN, 127.16oE, 167 m above sea level) is located about 35 km southeast of downtown Seoul. A PREDE skyradiometer (POM-02) is operated along with CIMEL sunphotometer (CE 318-1) to compare the aerosol optical properties derived from the two instruments. The operation for intercomparison study started with the DRAGON-Korea campaign and will continue for a year. POM-02 and CE 318-1 measure diffuse radiation at 6-minute intervals and 11 wavelengths and at 1-hour intervals and 4 wavelengths, respectively. Aerosol optical depths from these two instruments are compared at 440, 675, 870, and 1020 nm when the measurement time coincides within 3 minutes. Other aerosol optical properties such as Angstrom exponent and single scattering albedo (SSA) from the two instruments are also compared in a similar way. It is reported that SSA from the skyradiometer tends to be larger than that from sunphotometer. Factors causing the difference are closely examined.

  12. Aerosol Optical Properties and Component Extinction from Measurements on the Ronald H. Brown During ACE-Asia

    NASA Astrophysics Data System (ADS)

    Quinn, P. K.; Bates, T. S.; Coffman, D.; Miller, T.; Anderson, J.

    2002-12-01

    Measurements of aerosol chemical, physical, and optical properties were made onboard the NOAA R/V Ronald H. Brown during the ACE-Asia Intensive Field Program to characterize Asian aerosol as it was transported across the Pacific Ocean. The ship traveled across the Pacific from Hawaii to Japan and into the East China Sea and the Sea of Japan. Based on trajectory analysis, the aerosol has been categorized as remote marine, volcanic from the Miyakejima volcano, polluted from Korea and Japan, polluted from Beijing, polluted mixed with dust during post frontal conditions, and polluted mixed with dust from Shanghai and Korea. Presented here, for these different categories, are aerosol optical properties (scattering and absorption coefficients, single scattering albedo (SSA), Angstrom Exponent, and aerosol optical depth), mass fractions of the major chemical components, and mass extinction efficiencies and extinction coefficients for individual aerosol components. Lowest scattering and absorption coefficients and highest single scattering albedos were measured in marine air masses encountered as the ship transited from Hawaii toward Japan (mean SSA = 0.97). Lowest SSA were measured in polluted air masses from Korea and Japan (mean SSA = 0.90). With dust mixed into the polluted air masses, SSA increased due to the high scattering levels associated with the dust (mean SSA ranged from 0.92 to 0.96 for different pollution/dust mixtures). These SSA are for the sub-10 micron aerosol at 55 percent RH. They were 1 to 4 percent lower for the sub-1 micron aerosol. Unique to the ACE Asia aerosol was the observation of significant absorption at 550 nm by supermicron aerosol. A correlation between supermicron elemental carbon concentrations and the ratio of absorption by sub-1 um aerosol to absorption by sub-10 um aerosol suggests that supermicron EC is responsible. As the mean concentration of supermicron EC increased from the marine to polluted to polluted with dust cases, the ratio

  13. Extensive aerosol optical properties and aerosol mass related measurements during TRAMP/TexAQS 2006 - Implications for PM compliance and planning

    NASA Astrophysics Data System (ADS)

    Wright, Monica E.; Atkinson, Dean B.; Ziemba, Luke; Griffin, Robert; Hiranuma, Naruki; Brooks, Sarah; Lefer, Barry; Flynn, James; Perna, Ryan; Rappenglück, Bernhard; Luke, Winston; Kelley, Paul

    2010-10-01

    Extensive aerosol optical properties, particle size distributions, and Aerodyne quadrupole aerosol mass spectrometer measurements collected during TRAMP/TexAQS 2006 were examined in light of collocated meteorological and chemical measurements. Much of the evident variability in the observed aerosol-related air quality is due to changing synoptic meteorological situations that direct emissions from various sources to the TRAMP site near the center of the Houston-Galveston-Brazoria (HGB) metropolitan area. In this study, five distinct long-term periods have been identified. During each of these periods, observed aerosol properties have implications that are of interest to environmental quality management agencies. During three of the periods, long range transport (LRT), both intra-continental and intercontinental, appears to have played an important role in producing the observed aerosol. During late August 2006, southerly winds brought super-micron Saharan dust and sea salt to the HGB area, adding mass to fine particulate matter (PM 2.5) measurements, but apparently not affecting secondary particle growth or gas-phase air pollution. A second type of LRT was associated with northerly winds in early September 2006 and with increased ozone and sub-micron particulate matter in the HGB area. Later in the study, LRT of emissions from wildfires appeared to increase the abundance of absorbing aerosols (and carbon monoxide and other chemical tracers) in the HGB area. However, the greatest impacts on Houston PM 2.5 air quality are caused by periods with low-wind-speed sea breeze circulation or winds that directly transport pollutants from major industrial areas, i.e., the Houston Ship Channel, into the city center.

  14. Relations Between Cloud Condensation Nuclei And Aerosol Optical Properties Relevant to Remote Sensing: Airborne Measurements in Biomass Burning, Pollution and Dust Aerosol Over North America

    NASA Astrophysics Data System (ADS)

    Shinozuka, Y.; Clarke, A.; Howell, S.; Kapustin, V.; McNaughton, C.; Zhou, J.; Decarlo, P.; Jimenez, J.; Roberts, G.; Tomlinson, J.; Collins, D.

    2008-12-01

    Remote sensing of the concentration of cloud condensation nuclei (CCN) would help investigate the indirect effect of tropospheric aerosols on clouds and climate. In order to assess its feasibility, this paper evaluates the spectral-based retrieval technique for aerosol number and seeks one for aerosol solubility, using in-situ aircraft measurements of aerosol size distribution, chemical composition, hygroscopicity, CCN activity and optical properties. Our statistical analysis reveals that the CCN concentration over Mexico can be optically determined to a relative error of <20%, smaller than that for the mainland US and the surrounding oceans (~a factor of 2). Mexico's advantage is four-fold. Firstly, many particles originating from the lightly regulated industrial combustion and biomass burning are large enough to significantly affect light extinction, elevating the correlation between extinction and CCN number in absence of substantial dust. Secondly, the generally low ambient humidity near the major aerosol sources limits the error in the estimated response of particle extinction to humidity changes. Thirdly, because many CCN contain black carbon, light absorption also provides a measure of the CCN concentration. Fourthly, the organic fraction of volatile mass of submicron particles (OMF) is anti-correlated with the wavelength dependence of extinction due to preferential anion uptake by coarse dust, which provides a potential tool for remote-sensing OMF and the particle solubility.

  15. Aerosol Properties Derived from Airborne Sky Radiance and Direct Beam Measurements in Recent NASA and DoE Field Campaigns

    NASA Technical Reports Server (NTRS)

    Redemann, J.; Flynn, C. J.; Shinozuka, Y.; Russell, P. B.; Kacenelenbogen, M.; Segal-Rosenheimer, M.; Livingston, J. M.; Schmid, B.; Dunagan, S. E.; Johnson, R. R.; LeBlanc, S.; Schmidt, S.; Pilewskie, P.; Song, S.

    2014-01-01

    The AERONET (AErosol RObotic NETwork) ground-based suite of sunphotometers provides measurements of spectral aerosol optical depth (AOD), precipitable water and spectral sky radiance, which can be inverted to retrieve aerosol microphysical properties that are critical to assessments of aerosol-climate interactions. Because of data quality criteria and sampling constraints, there are significant limitations to the temporal and spatial coverage of AERONET data and their representativeness for global aerosol conditions.The 4STAR (Spectrometer for Sky-Scanning, Sun-Tracking Atmospheric Research) instrument, jointly developed by NASA Ames and PNNL (Pacific Northwest National Laboratory) with NASA Goddard collaboration, combines airborne sun tracking and AERONET-like sky scanning with spectroscopic detection. Being an airborne instrument, 4STAR has the potential to fill gaps in the AERONET data set. The 4STAR instrument operated successfully in the SEAC4RS (Studies of Emissions and Atmospheric Composition, Clouds and Climate Coupling by Regional Surveys) experiment in Aug./Sep. 2013 aboard the NASA DC-8 and in the DoE (Department of Energy)-sponsored TCAP (Two Column Aerosol Project, July 2012 & Feb. 2013) experiment aboard the DoE G-1 aircraft. 4STAR provided direct beam measurements of hyperspectral AOD, columnar trace gas retrievals (H2O, O3, NO2), and the first ever airborne hyperspectral sky radiance scans, which can be inverted to yield the same products as AERONET ground-based observations. In this presentation, we provide an overview of the new 4STAR capabilities, with an emphasis on 26 high-quality sky radiance measurements carried out by 4STAR in SEAC4RS. We compare collocated 4STAR and AERONET sky radiances, as well as their retrievals of aerosol microphysical properties for a subset of the available case studies. We summarize the particle property and air-mass characterization studies made possible by the combined 4STAR direct beam and sky radiance

  16. Aerosol properties derived from airborne sky radiance and direct beam measurements in recent NASA and DoE field campaigns

    NASA Astrophysics Data System (ADS)

    Redemann, J.; Flynn, C. J.; Shinozuka, Y.; Russell, P. B.; Kacenelenbogen, M. S.; Segal-Rosenhaimer, M.; Livingston, J. M.; Schmid, B.; Dunagan, S. E.; Johnson, R. R.; LeBlanc, S. E.; Schmidt, S.; Pilewskie, P.; Song, S.

    2014-12-01

    The AERONET (AErosol RObotic NETwork) ground-based suite of sunphotometers provides measurements of spectral aerosol optical depth (AOD), precipitable water and spectral sky radiance, which can be inverted to retrieve aerosol microphysical properties that are critical to assessments of aerosol-climate interactions. Because of data quality criteria and sampling constraints, there are significant limitations to the temporal and spatial coverage of AERONET data and their representativeness for global aerosol conditions. The 4STAR (Spectrometer for Sky-Scanning, Sun-Tracking Atmospheric Research) instrument, jointly developed by NASA Ames and PNNL with NASA Goddard collaboration, combines airborne sun tracking and AERONET-like sky scanning with spectroscopic detection. Being an airborne instrument, 4STAR has the potential to fill gaps in the AERONET data set. The 4STAR instrument operated successfully in the SEAC4RS [Studies of Emissions and Atmospheric Composition, Clouds and Climate Coupling by Regional Surveys] experiment in Aug./Sep. 2013 aboard the NASA DC-8 and in the DoE [Department of Energy]-sponsored TCAP [Two Column Aerosol Project, July 2012 & Feb. 2013] experiment aboard the DoE G-1 aircraft. 4STAR provided direct beam measurements of hyperspectral AOD, columnar trace gas retrievals (H2O, O3, NO2), and the first ever airborne hyperspectral sky radiance scans, which can be inverted to yield the same products as AERONET ground-based observations. In this presentation, we provide an overview of the new 4STAR capabilities, with an emphasis on 26 high-quality sky radiance measurements carried out by 4STAR in SEAC4RS. We compare collocated 4STAR and AERONET sky radiances, as well as their retrievals of aerosol microphysical properties for a subset of the available case studies. We summarize the particle property and airmass characterization studies made possible by the combined 4STAR direct beam and sky radiance observations.

  17. Climatology of aerosol and cloud optical properties at the Atmospheric Radiation Measurements Climate Research Facility Barrow and Atqasuk sites

    NASA Astrophysics Data System (ADS)

    Yin, Bangsheng; Min, Qilong

    2014-02-01

    The long-term measurements at the Barrow and Atqasuk sites have been processed to develop the climatology of aerosol and cloud properties at interannual, seasonal, and diurnal temporal scales. At the Barrow site, the surface temperature exhibits an increasing trend in both thawed and frozen seasons over the period studied here, about one decade. Corresponding to the warming, the snow melting day arrives earlier, and the non-snow-cover duration increases. Aerosol optical depth increased during 2001-2003 and 2005-2009 and decreased during 2003-2005. The liquid water path (LWP), cloud optical depth (COD), and cloud fraction exhibit apparently decreasing trends from 2002 to 2007 and increased significantly after 2008. In the frozen season, the arctic haze and ice clouds are dominant, while in the thawed season, the oceanic biogenic aerosols and liquid water clouds or mixed-phase clouds are dominant. The cloud droplet effective radius during the thawed season is larger than that during the frozen season. The diurnal variations of aerosol and cloud-related atmospheric properties are not obvious at these two sites. During the sunshine periods, the aerosol has a cooling effect on the surface through direct aerosol radiative forcing. In the frozen season, clouds have a positive impact on the net surface radiation, and the water vapor path, LWP, and COD have good positive correlations with the surface temperature, suggesting that the cloud radiation feedback is positive. In the thawed season, clouds have a negative impact on the net surface radiation.

  18. Retrieval of aerosol microphysical properties from AERONET photopolarimetric measurements: 1. Information content analysis

    NASA Astrophysics Data System (ADS)

    Xu, Xiaoguang; Wang, Jun

    2015-07-01

    This paper is the first part of a two-part study that aims to retrieve aerosol particle size distribution (PSD) and refractive index from the multispectral and multiangular polarimetric measurements taken by the new-generation Sun photometer as part of the Aerosol Robotic Network (AERONET). It provides theoretical analysis and guidance to the companion study in which we have developed an inversion algorithm for retrieving 22 aerosol microphysical parameters associated with a bimodal PSD function from real AERONET measurements. Our theoretical analysis starts with generating the synthetic measurements at four spectral bands (440, 675, 870, and 1020 nm) with a Unified Linearized Vector Radiative Transfer Model for various types of spherical aerosol particles. Subsequently, the quantitative information content for retrieving aerosol parameters is investigated in four observation scenarios, i.e., I1, I2, P1, and P2. Measurements in the scenario (I1) comprise the solar direct radiances and almucantar radiances that are used in the current AERONET operational inversion algorithm. The other three scenarios include different additional measurements: (I2) the solar principal plane radiances, (P1) the solar principal plane radiances and polarization, and (P2) the solar almucantar polarization. Results indicate that adding polarization measurements can increase the degree of freedom for signal by 2-5 in the scenario P1, while not as much of an increase is found in the scenarios I2 and P2. Correspondingly, smallest retrieval errors are found in the scenario P1: 2.3% (2.9%) for the fine-mode (coarse-mode) aerosol volume concentration, 1.3% (3.5%) for the effective radius, 7.2% (12%) for the effective variance, 0.005 (0.035) for the real-part refractive index, and 0.019 (0.068) for the single-scattering albedo. These errors represent a reduction from their counterparts in scenario I1 of 79% (57%), 76% (49%), 69% (52%), 66% (46%), and 49% (20%), respectively. We further

  19. Comparison of in situ and columnar aerosol spectral measurements during TexAQS-GoMACCS 2006: testing parameterizations for estimating aerosol fine mode properties

    NASA Astrophysics Data System (ADS)

    Atkinson, D. B.; Massoli, P.; O'Neill, N. T.; Quinn, P. K.; Brooks, S.; Lefer, B.

    2009-08-01

    During the 2006 Texas Air Quality Study and Gulf of Mexico Atmospheric Composition and Climate Study (TexAQS-GoMACCS 2006), the optical, chemical and microphysical properties of atmospheric aerosols were measured on multiple mobile platforms and at ground based stations. In situ measurements of the aerosol light extinction coefficient (σep) were performed by two multi-wavelength cavity ring-down (CRD) instruments, one located on board the NOAA R/V Ronald H. Brown (RHB) and the other located at the University of Houston, Moody Tower (UHMT). An AERONET sunphotometer was also located at the UHMT to measure the columnar aerosol optical depth (AOD). The σep data were used to extract the extinction Ångström exponent (åep), a measure of the wavelength dependence of σep. There was general agreement between the åep (and to a lesser degree σep measurements by the two spatially separated CRD instruments during multi-day periods, suggesting a regional scale consistency of the sampled aerosols. Two spectral models are applied to the σep and AOD data to extract the fine mode fraction of extinction (η) and the fine mode effective radius (Reff f). These two parameters are robust measures of the fine mode contribution to total extinction and the fine mode size distribution respectively. The results of the analysis are compared to Reff f values extracted using AERONET V2 retrievals and calculated from in situ particle size measurements on the RHB and at UHMT. During a time period when fine mode aerosols dominated the extinction over a large area extending from Houston/Galveston Bay and out into the Gulf of Mexico, the various methods for obtaining Reff f agree qualitatively (showing the same temporal trend) and quantitatively (pooled standard deviation=28 nm).

  20. Comparison of in situ and columnar aerosol spectral measurements during TexAQS-GoMACCS 2006: testing parameterizations for estimating aerosol fine mode properties

    NASA Astrophysics Data System (ADS)

    Atkinson, D. B.; Massoli, P.; O'Neill, N. T.; Quinn, P. K.; Brooks, S. D.; Lefer, B.

    2010-01-01

    During the 2006 Texas Air Quality Study and Gulf of Mexico Atmospheric Composition and Climate Study (TexAQS-GoMACCS 2006), the optical, chemical and microphysical properties of atmospheric aerosols were measured on multiple mobile platforms and at ground based stations. In situ measurements of the aerosol light extinction coefficient (σep) were performed by two multi-wavelength cavity ring-down (CRD) instruments, one located on board the NOAA R/V Ronald H. Brown (RHB) and the other located at the University of Houston, Moody Tower (UHMT). An AERONET sunphotometer was also located at the UHMT to measure the columnar aerosol optical depth (AOD). The σep data were used to extract the extinction Ångström exponent (åep), a measure of the wavelength dependence of σep. There was general agreement between the åep (and to a lesser degree σep) measurements by the two spatially separated CRD instruments during multi-day periods, suggesting a regional scale consistency of the sampled aerosols. Two spectral models are applied to the σep and AOD data to extract the fine mode fraction of extinction (η) and the fine mode effective radius (Reff,f). These two parameters are robust measures of the fine mode contribution to total extinction and the fine mode size distribution, respectively. The results of the analysis are compared to Reff,f values extracted using AERONET V2 retrievals and calculated from in situ particle size measurements on the RHB and at UHMT. During a time period when fine mode aerosols dominated the extinction over a large area extending from Houston/Galveston Bay and out into the Gulf of Mexico, the various methods for obtaining Reff,f agree qualitatively (showing the same temporal trend) and quantitatively (pooled standard deviation = 28 nm).

  1. Improvements in AOD retrieval from geostationary measurements over Asia with aerosol optical properties derived from the DRAGON-Asia campaign

    NASA Astrophysics Data System (ADS)

    Kim, M.; Kim, J.; Jeong, U.; Kim, W.; Holben, B.; Eck, T. F.; Lim, J. H.; Song, C. K.; Lee, S.

    2015-04-01

    An aerosol model optimized for East Asia is improved by applying inversion data from both long-term monitoring of the Aerosol Robotic Network (AERONET) sun photometer and the Distributed Regional Aerosol Gridded Observation Networks (DRAGON)-Asia campaign from 2012. This model plays an important role in retrieving accurate aerosol optical depth (AOD) from satellite-based measurements. In particular, the performance of a single visible channel algorithm, limited to a specific aerosol type, from real-time measurements is strongly affected by the assumed aerosol optical properties (AOPs) for the measured scene. In sensitivity tests, a 4% difference in single scattering albedo (SSA) between modeled and measured values can cause a retrieval error in AOD of over 20%, and the overestimation of SSA leads to an underestimation of AOD. Based on the AERONET inversion datasets obtained over East Asia before 2011, seasonally analyzed AOPs can be summarized by SSAs (measured at 675 nm) of 0.92, 0.94, 0.92, and 0.91 for spring (March, April, and May), summer (June, July, and August), autumn (September, October, and November), and winter (December, January, and February), respectively. After DRAGON-Asia 2012, the SSA during spring shows a slight increase to 0.93. The large volume of data and spatially concentrated measurements from this campaign can be used to improve the representative aerosol model for East Asia. Accordingly, the AOD datasets retrieved from a single channel algorithm, which uses a pre-calculated look-up table (LUT) with the new aerosol model, show an improved correlation with the measured AOD during the DRAGON-Asia campaign (March to May 2012). Compared with the correlation of the AOD retrieved using the original aerosol model, the regression slope between the new AOD and the AERONET values is reduced from 1.08 to 1.00, while the change of the y-offset of -0.08 is significant. The correlation coefficients for the comparisons are 0.87 and 0.85, respectively. The

  2. Retrieval of aerosol properties over land surfaces: capabilities of multiple-viewing-angle intensity and polarization measurements

    NASA Astrophysics Data System (ADS)

    Hasekamp, Otto P.; Landgraf, Jochen

    2007-06-01

    We investigate the capabilities of different instrument concepts for the retrieval of aerosol properties over land. It was found that, if the surface reflection properties are unknown, only multiple-viewing-angle measurements of both intensity and polarization are able to provide the relevant aerosol parameters with sufficient accuracy for climate research. Furthermore, retrieval errors are only little affected when the number of viewing angles is increased at the cost of the number of spectral sampling points and vice versa. This indicates that there is a certain amount of freedom for the instrument design of dedicated aerosol instruments. The final choice on the trade-off between the spectral sampling and the number of viewing angles should be made taking other factors into account, such as instrument complexity and the ability to obtain global coverage.

  3. A new method of measuring aerosol optical properties from digital twilight photographs

    NASA Astrophysics Data System (ADS)

    Saito, M.; Iwabuchi, H.

    2015-10-01

    An optimal-estimation algorithm for inferring aerosol optical properties from digital twilight photographs is proposed. The sensitivity of atmospheric components and surface characteristics to brightness and color of twilight sky is investigated, and the results suggest that tropospheric and stratospheric aerosol optical thickness (AOT) are sensitive to condition of the twilight sky. The coarse-fine particle volume ratio is moderately sensitive to the sky condition near the horizon under a clean-atmosphere condition. A radiative transfer model that takes into account a spherical-shell atmosphere, refraction, and multiple scattering is used as a forward model. Error analysis shows that the tropospheric and stratospheric AOT can be retrieved without significant bias. Comparisons with results from other ground-based instruments exhibit reasonable agreement on AOT. A case study suggests that the AOT retrieval method can be applied to atmospheric conditions with varying aerosol vertical profiles and vertically inhomogeneous species in the troposphere.

  4. A new method of measuring aerosol optical properties from digital twilight photographs

    NASA Astrophysics Data System (ADS)

    Saito, M.; Iwabuchi, H.

    2015-01-01

    An optimal-estimation algorithm for inferring aerosol optical properties from digital twilight photographs is proposed. The sensitivity of atmospheric components and surface characteristics to brightness and color of twilight sky is investigated, and the results suggest that tropospheric and stratospheric aerosol optical thickness (AOT) are sensitive to condition of the twilight sky. The coarse-fine particle volume ratio is moderately sensitive to the sky condition near the horizon under a clean-atmosphere condition. A radiative transfer model that takes into account a spherical-shell atmosphere, refraction, and multiple scattering is used as a forward model. Error analysis shows that the tropospheric and stratospheric AOT can be retrieved without significant bias. Comparisons with results from other ground-based instruments exhibit reasonable agreement on AOT. A case study suggests that the AOT retrieval method can be applied to atmospheric conditions with varying aerosol vertical profiles and vertically inhomogeneous species in the troposphere.

  5. A comparison of measured and calculated optical properties of atmospheric aerosols at infrared wavelengths

    NASA Technical Reports Server (NTRS)

    Rosen, James M.

    1991-01-01

    Measurements of 10.6-micron lidar backscatter were compared with calculated backscatter based on nearly simultaneous observations of stratospheric and tropospheric aerosol size distributions. It was found that there is better agreement in the troposphere, even though the uncertainties of the calculation are greater for this region due to the variables in both the spatial concentration and the physical makeup of the aerosol. A second comparison study was made to test the consistency of the mean tropospheric extinction values at 1.02 micron (as reported by the SAGE satellite) with the values calculated from an ensemble of 400 measured size distributions thought to be representative of midcontinental tropospheric aerosol. The two methods produce consistent results within the expected degree of uncertainty. The ensemble of 400 'proven' size distributions is then used to calculate a statistical relationship between the 1.02-micron extinction and the 10.6-micron backscatter.

  6. Global Measurement of Junge Layer Stratospheric Aerosol with OMPS/LP. Scattering Properties and Particle Size

    NASA Astrophysics Data System (ADS)

    Rault, D. F.; Bhartia, P. K.

    2014-12-01

    The OMPS/LP was launched on board the NPP space platform in October 2011. Over the past two years, the OMPS/LP was used to retrieve the global distribution of ozone and aerosol. The paper will describe the aerosol product, which NASA is presently preparing for public release. The current OMPS/LP aerosol product consists of latitude-altitude curtains along the NPP Sun-synchronous orbit, from cloud top to about 40 km. These curtains extend from local sunrise in Southern polar region to local sunset in Northern polar region. Aerosol extinctions are produced at five distinct wavelengths, namely 513, 525, 670, 750 and 870 nm, with a sampling of 1 km in vertical direction and 1 degree latitude in the along-track direction. The OMPS/LP aerosol dataset is fairly large, with 7000 vertical profiles produced each day for each wavelength. The aerosol product will be presented in terms of extinction monthly median values and mean Angstrom coefficient (particle size). Over the past two years, the Junge layer was affected by several events such as volcanic eruptions (Nabro and Kelut) and a meteor (Chelyabinsk), the effects of which are clearly visible in the OMPS/LP dataset. The Asian Tropopause Aerosol Layer (ATAL) can also be observed in the OMPS/LP dataset. Moreover the effect of the Brewer Dobson Circulation (BDC) can be observed at high altitudes: the BDC velocity at 35 km can be estimated from the time variation of iso-density heights and was found to compare well with BDC velocities evaluated with the water vapor tape recorder technique as well as MERRA model values. Finally, aerosol filaments are clearly visible in OMPS/LP aerosol dataset as they appear as distinct "bubbles" on the OMPS/LP curtain files at periodic intervals in both the Southern and Northern hemispheres. These filaments are a main source of transport from tropical to polar region, and OMPS/LP data can therefore be instrumental in quantifying the rate of this transport. The quality of the OMPS/LP aerosol

  7. Deriving aerosol properties from measurements of the Atmosphere-Surface Radiation Automatic Instrument (ASRAI)

    NASA Astrophysics Data System (ADS)

    Xu, Hua; Li, Donghui; Li, Zhengqiang; Zheng, Xiaobing; Li, Xin; Xie, Yisong; Liu, Enchao

    2015-10-01

    The Atmosphere-surface Radiation Automatic Instrument (ASRAI) is a newly developed hyper-spectral apparatus by Anhui Institute of Optics and Fine Mechanics, Chinese Academy of Sciences (AIOFM, CAS), measuring total spectral irradiance, diffuse spectral irradiance of atmosphere and reflected radiance of the land surface for the purpose of in-situ calibration. The instrument applies VIS-SWIR spectrum (0.4~1.0 μm) with an averaged spectral resolution of 0.004 μm. The goal of this paper is to describe a method of deriving both aerosol optical depth (AOD) and aerosol modes from irradiance measurements under free cloudy conditions. The total columnar amounts of water vapor and oxygen are first inferred from solar transmitted irradiance at strong absorption wavelength. The AOD together with total columnar amounts of ozone and nitrogen dioxide are determined by a nonlinear least distance fitting method. Moreover, it is able to infer aerosol modes from the spectral dependency of AOD because different aerosol modes have their inherent spectral extinction characteristics. With assumption that the real aerosol is an idea of "external mixing" of four basic components, dust-like, water-soluble, oceanic and soot, the percentage of volume concentration of each component can be retrieved. A spectrum matching technology based on Euclidean-distance method is adopted to find the most approximate combination of components. The volume concentration ratios of four basic components are in accordance with our prior knowledge of regional aerosol climatology. Another advantage is that the retrievals would facilitate the TOA simulation when applying 6S model for satellite calibration.

  8. The Atmospheric Radiation Measurement Program May 2003 Intensive Operations Period Examining Aerosol Properties and Radiative Influences: Preface to Special Section

    NASA Technical Reports Server (NTRS)

    Ferrare, Richard; Feingold, Graham; Ghan, Steven; Ogren, John; Schmid, Beat; Schwartz, Stephen E.; Sheridan, Pat

    2006-01-01

    Atmospheric aerosols influence climate by scattering and absorbing radiation in clear air (direct effects) and by serving as cloud condensation nuclei, modifying the microphysical properties of clouds, influencing radiation and precipitation development (indirect effects). Much of present uncertainty in forcing of climate change is due to uncertainty in the relations between aerosol microphysical and optical properties and their radiative influences (direct effects) and between microphysical properties and their ability to serve as cloud condensation nuclei at given supersaturations (indirect effects). This paper introduces a special section that reports on a field campaign conducted at the Department of Energy Atmospheric Radiation Measurement site in North Central Oklahoma in May, 2003, examining these relations using in situ airborne measurements and surface-, airborne-, and space-based remote sensing.

  9. Shortwave Radiative Fluxes, Solar-Beam Transmissions, and Aerosol Properties: TARFOX and ACE-2 Find More Absorption from Flux Radiometry than from Other Measurements

    NASA Technical Reports Server (NTRS)

    Russell, Philip B.; Redemann, J.; Schmid, B.; Livingston, J. M.; Bergstrom, R. W.; Ramirez, S. A.; Hipskind, R. Stephen (Technical Monitor)

    2001-01-01

    The Tropospheric Aerosol Radiative Forcing Observational Experiment (TARFOX) and the Second Aerosol Characterization Experiment (ACE-2) made simultaneous measurements of shortwave radiative fluxes, solar-beam transmissions, and the aerosols affecting those fluxes and transmissions. Besides the measured fluxes and transmissions, other obtained properties include aerosol scattering and absorption measured in situ at the surface and aloft; aerosol single scattering albedo retrieved from skylight radiances; and aerosol complex refractive index derived by combining profiles of backscatter, extinction, and size distribution. These measurements of North Atlantic boundary layer aerosols impacted by anthropogenic pollution revealed the following characteristic results: (1) Better agreement among different types of remote measurements of aerosols (e.g., optical depth, extinction, and backscattering from sunphotometers, satellites, and lidars) than between remote and in situ measurements; 2) More extinction derived from transmission measurements than from in situ measurements; (3) Larger aerosol absorption inferred from flux radiometry than from other measurements. When the measured relationships between downwelling flux and optical depth (or beam transmission) are used to derive best-fit single scattering albedos for the polluted boundary layer aerosol, both TARFOX and ACE-2 yield midvisible values of 0.90 +/- 0.04. The other techniques give larger single scattering albedos (i.e. less absorption) for the polluted boundary layer, with a typical result of 0.95 +/- 0.04. Although the flux-based results have the virtue of describing the column aerosol unperturbed by sampling, they are subject to questions about representativeness and other uncertainties (e.g., unknown gas absorption). Current uncertainties in aerosol single scattering albedo are large in terms of climate effects. They also have an important influence on aerosol optical depths retrieved from satellite radiances

  10. Retrieval of Aerosol Microphysical Properties from AERONET Photo-Polarimetric Measurements. 2: A New Research Algorithm and Case Demonstration

    NASA Technical Reports Server (NTRS)

    Xu, Xiaoguang; Wang, Jun; Zeng, Jing; Spurr, Robert; Liu, Xiong; Dubovik, Oleg; Li, Li; Li, Zhengqiang; Mishchenko, Michael I.; Siniuk, Aliaksandr; Holben, Brent N.

    2015-01-01

    A new research algorithm is presented here as the second part of a two-part study to retrieve aerosol microphysical properties from the multispectral and multiangular photopolarimetric measurements taken by Aerosol Robotic Network's (AERONET's) new-generation Sun photometer. The algorithm uses an advanced UNified and Linearized Vector Radiative Transfer Model and incorporates a statistical optimization approach.While the new algorithmhas heritage from AERONET operational inversion algorithm in constraining a priori and retrieval smoothness, it has two new features. First, the new algorithmretrieves the effective radius, effective variance, and total volume of aerosols associated with a continuous bimodal particle size distribution (PSD) function, while the AERONET operational algorithm retrieves aerosol volume over 22 size bins. Second, our algorithm retrieves complex refractive indices for both fine and coarsemodes,while the AERONET operational algorithm assumes a size-independent aerosol refractive index. Mode-resolved refractive indices can improve the estimate of the single-scattering albedo (SSA) for each aerosol mode and thus facilitate the validation of satellite products and chemistry transport models. We applied the algorithm to a suite of real cases over Beijing_RADI site and found that our retrievals are overall consistent with AERONET operational inversions but can offer mode-resolved refractive index and SSA with acceptable accuracy for the aerosol composed by spherical particles. Along with the retrieval using both radiance and polarization, we also performed radiance-only retrieval to demonstrate the improvements by adding polarization in the inversion. Contrast analysis indicates that with polarization, retrieval error can be reduced by over 50% in PSD parameters, 10-30% in the refractive index, and 10-40% in SSA, which is consistent with theoretical analysis presented in the companion paper of this two-part study.

  11. Retrieval of aerosol microphysical properties from AERONET photopolarimetric measurements: 2. A new research algorithm and case demonstration

    NASA Astrophysics Data System (ADS)

    Xu, Xiaoguang; Wang, Jun; Zeng, Jing; Spurr, Robert; Liu, Xiong; Dubovik, Oleg; Li, Li; Li, Zhengqiang; Mishchenko, Michael I.; Siniuk, Aliaksandr; Holben, Brent N.

    2015-07-01

    A new research algorithm is presented here as the second part of a two-part study to retrieve aerosol microphysical properties from the multispectral and multiangular photopolarimetric measurements taken by Aerosol Robotic Network's (AERONET's) new-generation Sun photometer. The algorithm uses an advanced UNified and Linearized Vector Radiative Transfer Model and incorporates a statistical optimization approach. While the new algorithm has heritage from AERONET operational inversion algorithm in constraining a priori and retrieval smoothness, it has two new features. First, the new algorithm retrieves the effective radius, effective variance, and total volume of aerosols associated with a continuous bimodal particle size distribution (PSD) function, while the AERONET operational algorithm retrieves aerosol volume over 22 size bins. Second, our algorithm retrieves complex refractive indices for both fine and coarse modes, while the AERONET operational algorithm assumes a size-independent aerosol refractive index. Mode-resolved refractive indices can improve the estimate of the single-scattering albedo (SSA) for each aerosol mode and thus facilitate the validation of satellite products and chemistry transport models. We applied the algorithm to a suite of real cases over Beijing_RADI site and found that our retrievals are overall consistent with AERONET operational inversions but can offer mode-resolved refractive index and SSA with acceptable accuracy for the aerosol composed by spherical particles. Along with the retrieval using both radiance and polarization, we also performed radiance-only retrieval to demonstrate the improvements by adding polarization in the inversion. Contrast analysis indicates that with polarization, retrieval error can be reduced by over 50% in PSD parameters, 10-30% in the refractive index, and 10-40% in SSA, which is consistent with theoretical analysis presented in the companion paper of this two-part study.

  12. Surface measurements of aerosol properties over northwest China during ARM China 2008 deployment

    NASA Astrophysics Data System (ADS)

    Wang, Xin; Huang, Jiangping; Zhang, Rudong; Chen, Bin; Bi, Jianrong

    2010-04-01

    To improve understanding and capture the direct evidence of the impact of dust aerosol on climate, the 2008 China-U.S. joint field campaigns are conducted. Three sites are involved this campaign, including one permanent site (Semi-Arid Climate and Environment Observatory of Lanzhou University (SACOL)) (located in Yuzhong, 35.95°N, 104.1°E), one SACOL's Mobile Facility (SMF) (deployed in Jintai, 37.57°N, 104.23°E), and the U.S. Department of Energy Atmospheric Radiation Measurements (ARM) Ancillary Facility (AAF mobile laboratories, SMART-COMMIT) (deployed in Zhangye, 39.08°N, 100.27°E). This paper presents the results of direct measurement analysis of the dust plume transport case. During the dust plume period, the OMI AI data and air mass back trajectory model (HYSPLIT) clearly illustrated that the air mass originated from the Taklamakan desert and Inner Mongolia Gobi desert. The daily averaged concentrations of PM10 were about 0.2 ± 0.03 mg/m3 at SACOL and Zhangye, but during the dust plume the mass concentration of dust aerosol were 0.98 mg/m3 at Zhangye and 0.52 mg/m3 at SACOL. The black carbon (BC) value reached its high peak during the dust plume. However, the concentration of BC was not only fluctuated with the dust plume, but also affected by the local air pollutants. When the dust plume occurred, the multiwavelength aerosol optical depth can be raised to ˜2, ˜1.5 times as high as that during the non dust plume period, and the number (mass) distribution during the dust plume showed the aerosol types considered correspond to urban/industrial aerosols, coarse mode particles. The meteorological analysis indicated that these polluted layers are not only transported from their sources, but also include the local sources.

  13. 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

  14. In situ measurements of aerosol mass concentration and radiative properties in Xianghe, southeast of Beijing

    NASA Astrophysics Data System (ADS)

    Chaudhry, Zahra; Martins, J. Vanderlei; Li, Zhanqing; Tsay, Si-Chee; Chen, Hongbin; Wang, Pucai; Wen, Tianxue; Li, Can; Dickerson, Russell R.

    2007-12-01

    As a part of the EAST-AIRE study, Nuclepore filters were collected in two size ranges (coarse, 2.5 μm < d < 10 μm, and fine, d < 2.5 μm) from January to May 2005 in Xianghe, about 70 km southeast of Beijing, and analyzed for aerosol mass concentration, spectral absorption efficiency and absorption coefficient. Twelve-hour aerosol mass concentration measurements showed an average concentration of 120 μg/m3 in the coarse mode and an average concentration of 25 μg/m3 in the fine mode. To determine how representative ground-based measurements are of the total column, the mass concentration data was compared with AERONET AOT at 500 nm and AERONET size distribution data. The vertical distribution of the aerosols were studied with a micropulse lidar and in the cases where the vertical column was found to be fairly homogenous, the comparisons of the filter results with AERONET agreed favorably, while in the cases of inhomogeneity, the comparisons have larger disagreement. For fine mode aerosols, the average spectral absorption efficiency equates well to a λ-1 model, while the coarse mode shows a much flatter spectral dependence, consistent with large particle models. The coarse mode absorption efficiency was compatible with that of the fine mode in the NIR region, indicating the much stronger absorption of the coarse mode due to its composition and sizable mass. Single scattering albedo results are presented from a combination between absorption coefficients derived from the filter measurements, from a PSAP and from a three-wavelength Nephelometer.

  15. Detailed Aerosol Characterization using Polarimetric Measurements

    NASA Astrophysics Data System (ADS)

    Hasekamp, Otto; di Noia, Antonio; Stap, Arjen; Rietjens, Jeroen; Smit, Martijn; van Harten, Gerard; Snik, Frans

    2016-04-01

    Anthropogenic aerosols are believed to cause the second most important anthropogenic forcing of climate change after greenhouse gases. In contrast to the climate effect of greenhouse gases, which is understood relatively well, the negative forcing (cooling effect) caused by aerosols represents the largest reported uncertainty in the most recent assessment of the International Panel on Climate Change (IPCC). To reduce the large uncertainty on the aerosol effects on cloud formation and climate, accurate satellite measurements of aerosol optical properties (optical thickness, single scattering albedo, phase function) and microphysical properties (size distribution, refractive index, shape) are essential. There is growing consensus in the aerosol remote sensing community that multi-angle measurements of intensity and polarization are essential to unambiguously determine all relevant aerosol properties. This presentations adresses the different aspects of polarimetric remote sensing of atmospheric aerosols, including retrieval algorithm development, validation, and data needs for climate and air quality applications. During past years, at SRON-Netherlands Instite for Space Research retrieval algorithms have been developed that make full use of the capabilities of polarimetric measurements. We will show results of detailed aerosol properties from ground-based- (groundSPEX), airborne- (NASA Research Scanning Polarimeter), and satellite (POLDER) measurements. Also we will discuss observational needs for future instrumentation in order to improve our understanding of the role of aerosols in climate change and air quality.

  16. Analysis of aerosol optical properties from continuous sun-sky radiometer measurements at Halley and Rothera, Antarctica over seven years

    NASA Astrophysics Data System (ADS)

    Campanelli, Monica; Estellés, Victor; Colwell, Steve; Shanklin, Jonathan; Ningombam, Shantikumar S.

    2015-04-01

    The Antarctic continent is located far from most anthropogenic emission sources on the planet, it has limited areas of exposed rock and human activities are less developed. Air circulation over Antarctica also seems to prevent the direct transport of air originating from anthropogenic sources of pollution at lower latitudes. Therefore Antarctica is considered an attractive site for studying aerosol properties as unaltered as possible by human activity. Long term monitoring of the optical and physical properties is necessary for observing possible changes in the atmosphere over time and understanding if such changes are due to human activity or natural variation. Columnar aerosol optical and physical properties can be obtained from sun-sky radiometers, very compact instruments measuring spectral direct and diffuse solar irradiance at the visible wavelengths and using fast and efficient inversion algorithms. The British Antarctic Survey has continuously operated two Prede Pom-01 sun-sky radiometers in Antarctica as part of the ESR-European Skynet Radiometers network (www.euroskyrad.net, Campanelli et al, 2012). They are located at Halley and Rothera, and have operated since 2009 and 2008 respectively. In the present study the aerosol optical thickness, single scattering albedo, Ångström exponent, volume size distribution and refractive index were retrieved from cloud-screened measurements of direct and diffuse solar irradiance using the Skyrad 4.2 pack code (Nakajima et al., 1986). The analysis of the daily and yearly averages showed an important increase of the absorbing properties of particles at Halley from 2013 to the beginning of 2014 related to the increasing presence of smaller particles (from 2012) but with a non-significant variation of aerosol optical depth. The same increase of absorption was visible at Rothera only in 2013. Air pressure measurements, wind directions and intensity, and vertical profiles from radio-soundings, together with HYSPLIT model

  17. Development and Assessment of a Neural Network Approach for Retrieving Aerosol Properties from Multispectral, Multiangle Polarization Measurements

    NASA Astrophysics Data System (ADS)

    Tucker-Simmons, Matthew

    Quantifying the microphysical properties of aerosols is crucial for quantifying global climate forcings. Satellite based aerosol retrievals usually rely on intensity measurements of the scattered light, but this approach has been proven inadequate for retrieving the complex refractive index and shape of aerosols, as well as the contamination from the ground surfaces. It is with these limitations in mind that we plan to improve the quality and scope of aerosol retrievals, by making use of the full capabilities of current and future polarimetric sensor systems. In order to utilize the increased information content on aerosol optical thickness (AOT), size distribution, shape and single scattering albedo (SSA), intrinsically available in multispectral-multiangle polarimetric observations, we make use of suitably constructed neural networks (NNs). We focus our analysis initially on simple retrievals over the ocean, in order to best assess the potential of the NNs as a practical approach and to identify any possible limitations. In particular, we find that, by choosing a suitable combination of inputs and outputs, based on principal component analysis (PCA), we can develop a robust NN retrieval trained on synthetic datasets. We further show the value of using cascaded NNs, to improve retrieval accuracy. Consequently, we demonstrate the potential and limitations of this approach on real aircraft instrument data from the Research Scanning Polarimeter (RSP). Discrepancies in the retrievals are found to be due to limitations from the use of spherical particle assumptions and preliminary efforts to overcome this restriction are identified. It is our belief that the value of these methods, in comparison to existing local inversion schemes, will further increase with the expected magnification of data sizes on future missions, such as the Aerosol-Cloud-Ecosystem (ACE) Mission.

  18. In-Situ Measurements of Aerosol Optical and Hygroscopic Properties at the Look Rock Site during SOAS 2013

    NASA Astrophysics Data System (ADS)

    Zhang, X.; Zimmermann, K.; Bertram, T. H.; Corrigan, A. L.; Guzman, J. M.; Russell, L. M.; Budisulistiorini, S.; Li, X.; Surratt, J. D.; Hicks, W.; Bairai, S. T.; Cappa, C. D.

    2013-12-01

    One of the main goals of the Southern Oxidant and Aerosol Study (SOAS) is to characterize the climate-relevant properties of aerosols over the southeastern United States at the interface of biogenic and anthropogenic emissions. As part of the SOAS campaign, the UCD cavity ringdown/photoacoustic spectrometer was deployed to make in-situ measurements of aerosol light extinction, absorption and sub-saturated hygroscopicity at the Look Rock site (LRK) in the Great Smoky Mountains National Park, TN from June 1 to July 15, 2013. The site is influenced by substantial biogenic emissions with varying impacts from anthropogenic pollutants, allowing for direct examination of the optical and hygroscopic properties of anthropogenic-influenced biogenic secondary organic aerosols (SOA). During the experiment period, the average dry aerosol extinction (Bext), absorption (Babs) coefficients and single scattering albedo (SSA) at 532 nm were 30.3 × 16.5 Mm-1, 1.12 × 0.78 Mm-1 and 0.96 × 0.06. The Babs at 532 nm was well correlated (r2 = 0.79) with the refractory black carbon (rBC) number concentration determined by a single particle soot spectrometer (SP2). The absorption by black carbon (BC), brown carbon (BrC) and the absorption enhancement due to the 'lensing' effect were quantified by comparing the Babs of ambient and thermo-denuded aerosols at 405 nm and 532 nm. The optical sub-saturated hygroscopic growth factor was derived from extinction and particle size distribution measurements at dry and elevated relative humidity. In addition, to explore the extent to which ammonia mediated chemistry leads to BrC formation, as suggested in recent laboratory studies(1,2), we performed an NH3 perturbation experiment in-situ for 1 week during the study, in which ambient aerosols were exposed to approximately 100 ppb NH3 with a residence time of ~ 3hr. The broader implications of these observational data at LRK will be discussed in the context of the concurrent gas and aerosol chemical

  19. 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.

    PubMed

    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

    2002-12-20

    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 band, 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 measurement of the various instruments. It seems then that the log-normal assumption cannot fully reproduce the size distribution of background aerosols. The effect ofthe presence of particular aerosols on the measurements is discussed, and a new strategy for observations is proposed.

  20. Optical properties of different aerosol types: seven years of combined Raman- elastic backscatter lidar measurements in Thessaloniki, Greece

    NASA Astrophysics Data System (ADS)

    Giannakaki, E.; Balis, D. S.; Amiridis, V.; Zerefos, C.

    2009-11-01

    We present our combined Raman/elastic backscatter lidar observations which were carried out at the EARLINET station of Thessaloniki, Greece, during the period 2001-2007. The largest optical depths are observed for Saharan dust and smoke aerosol loads. For "local" and "continental polluted" aerosols the measurements indicate moderate aerosol loads. However, measurements associated with the "local" path show lower values of free tropospheric contribution (37% versus 46% for "continental polluted") and thus, enhanced aerosol load within the Planetary Boundary Layer. The lowest value of aerosol optical depth is observed for "continental clean" aerosols. The largest lidar ratios, of the order of 70 sr are found for biomass burning aerosols. A significant and distinct correlation between lidar ratio and backscatter related Ångström exponent values was estimated for well defined aerosol categories, which provides a statistical measure of the lidar ratio's dependency on aerosol-size, which is a useful tool for elastic lidar systems. Scatter plot between lidar ratio values and Ångström exponent values for "local" and "continental polluted" aerosols does not show a significant correlation, with a large variation in both parameters possibly due to variable absorption characteristics of these aerosols. Finally for "clean continental" aerosols we found constantly low lidar ratios almost independent of size.

  1. Water Vapor, Cloud and Aerosol Properties on the Tibetan Plateau Using Multi-Lidar Measurements

    NASA Astrophysics Data System (ADS)

    Wu, Songhua; Dai, Guangyao; Wang, Dongxiang; Zhai, Xiaochun; Song, Xiaoquan

    2016-06-01

    The 3rd Tibetan Plateau atmospheric expedition experiment campaign were operated in the Tibetan Plateau during July and August 2014 by utilizing the Water vapor, Cloud and Aerosol Lidar (WVCAL), Coherent Doppler Wind Lidar and ceilometer VAISALA CL31. The observation was carried out in Nagqu area (31.5°N, 92.05°E), which is 4508 meters above the mean sea level. Water vapor mixing ratio, cloud height, vertical wind speed and vertical water vapor flux was measured by these lidars. The inversion methods of data products of lidars are described in details in this paper. Furthermore, the clouds heights measured by lidar and ceilometer were compared to verify the performance of the lidar. Finally, the case studies of water vapor mixing ratio, water vapor flux and cloud height and statistics were provided.

  2. In situ measurements of aerosols optical properties and number size distributions in a subarctic coastal region of Norway

    NASA Astrophysics Data System (ADS)

    Mogo, S.; Cachorro, V. E.; Lopez, J. F.; Montilla, E.; Torres, B.; Rodríguez, E.; Bennouna, Y.; de Frutos, A. M.

    2011-12-01

    In situ measurements of aerosol optical properties were made in the summer of 2008 at the ALOMAR station facility (69°16 N, 16°00 E), located at a rural site in the north of the island of Andøya (Vesterålen archipelago), approximately 300 km north of the Arctic Circle. The extended three-month campaign was part of the POLARCAT Project (Polar Study using Aircraft, Remote Sensing, Surface Measurements and Models, of Climate, Chemistry, Aerosols, and Transport) of the International Polar Year (IPY-2007-2008). Its goal was to characterize the aerosols of this sub-Arctic area, which are frequently transported to the Arctic region. The ambient light-scattering coefficient, σs (550 nm), at ALOMAR had a measured hourly mean value of 5.41 Mm-1 (StD = 3.55 Mm-1), and the light-absorption coefficient, σa (550 nm), had a measured hourly mean value of 0.40 Mm-1 (StD = 0.27 Mm-1). The scattering/absorption Ångström exponents, αs,a, are used for a detailed analysis of the variations of the spectral shape of σs,a. Whereas αs demonstrates the presence of two particle sizes corresponding to two types of aerosols, the αa demonstrates only one type of absorbing aerosol particles. Values of αa above 1 were not observed. The single-scattering albedo, ω0, ranged from 0.62 to 0.99 (mean = 0.91, StD = 0.05), and the relationships of this property to the absorption/scattering coefficients and the Ångström exponents are presented. The concentration of the particles was monitored using a scanning mobility particle sizer (SMPS), an aerodynamic particle sizer (APS) and an ultrafine condensation particle counter (UCPC). The shape of the median size distribution of the particles in the submicrometer fraction was bimodal, and the submicrometer, micrometer and total concentrations presented hourly mean values of 1277 cm3 (StD = 1563 cm3), 1 cm3 (StD = 1 cm3) and 2463 cm3 (StD = 4251 cm3), respectively. The modal correlations were investigated, and the concentration of particles

  3. Remote sensing of aerosol properties during CARES

    NASA Astrophysics Data System (ADS)

    Kassianov, Evgueni; Barnard, James; Pekour, Mikhail; Flynn, Connor; Ferrare, Richard; Hostetler, Chris; Hair, John; Jobson, Bertram T.

    2011-11-01

    One month of MFRSR data collected at two sites in the central California (USA) region during the CARES campaign are processed and the MFRSR-derived AODs at 500 nm wavelength are compared with available AODs provided by AERONET measurements. We find that the MFRSR and AERONET AODs are small (~0.05) and comparable. A reasonable quantitative agreement between column aerosol size distributions (up to 2 μm) from the MFRSR and AERONET retrievals is illustrated as well. Analysis of the retrieved (MFRSR and AERONET) and in situ measured aerosol size distributions suggests that the contribution of the coarse mode to aerosol optical properties is substantial for several days. The results of a radiative closure experiment performed for the two sites and one-month period show a favorable agreement between the calculated and measured broadband downwelling irradiances (bias does not exceed about 3 Wm-2), and thus imply that the MFRSR-derived aerosol optical properties are reasonable.

  4. Remote Sensing of Aerosol Properties during CARES

    SciTech Connect

    Kassianov, Evgueni I.; Barnard, James C.; Pekour, Mikhail S.; Flynn, Connor J.; Ferrare, R.; Hostetler, Chris A.; Hair, John; Jobson, Bertram Thomas

    2011-10-01

    One month of MFRSR data collected at two sites in the central California (USA) region during the CARES campaign are processed and the MFRSR-derived AODs at 500 nm wavelength are compared with available AODs provided by AERONET measurements. We find that the MFRSR and AERONET AODs are small ({approx}0.05) and comparable. A reasonable quantitative agreement between column aerosol size distributions (up to 2 um) from the MFRSR and AERONET retrievals is illustrated as well. Analysis of the retrieved (MFRSR and AERONET) and in situ measured aerosol size distributions suggests that the contribution of the coarse mode to aerosol optical properties is substantial for several days. The results of a radiative closure experiment performed for the two sites and one-month period show a favorable agreement between the calculated and measured broadband downwelling irradiances (bias does not exceed about 3 Wm-2), and thus imply that the MFRSR-derived aerosol optical properties are reasonable.

  5. The CU 2-D-MAX-DOAS instrument - Part 2: Raman scattering probability measurements and retrieval of aerosol optical properties

    NASA Astrophysics Data System (ADS)

    Ortega, Ivan; Coburn, Sean; Berg, Larry K.; Lantz, Kathy; Michalsky, Joseph; Ferrare, Richard A.; Hair, Johnathan W.; Hostetler, Chris A.; Volkamer, Rainer

    2016-08-01

    The multiannual global mean of aerosol optical depth at 550 nm (AOD550) over land is ˜ 0.19, and that over oceans is ˜ 0.13. About 45 % 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. We present an inherently calibrated retrieval (i.e., no need for radiance calibration) to simultaneously measure AOD and the aerosol phase function parameter, g, based on measurements of azimuth distributions of the Raman scattering probability (RSP), the near-absolute rotational Raman scattering (RRS) intensity. We employ radiative transfer model simulations to show that for solar azimuth RSP measurements at solar elevation and solar zenith angle (SZA) smaller than 80°, RSP is insensitive to the vertical distribution of aerosols and maximally sensitive to changes in AOD and g under near-molecular scattering conditions. The University of Colorado two-dimensional Multi-AXis Differential Optical Absorption Spectroscopy (CU 2-D-MAX-DOAS) instrument was deployed as part of the Two Column Aerosol Project (TCAP) at Cape Cod, MA, during the summer of 2012 to measure direct sun spectra and RSP from scattered light spectra at solar relative azimuth angles (SRAAs) between 5 and 170°. During two case study days with (1) high aerosol load (17 July, 0.3 < AOD430 < 0.6) and (2) near-molecular scattering conditions (22 July, AOD430 < 0.13) we compare RSP-based retrievals of AOD430 and g with data from a co-located CIMEL sun photometer, Multi-Filter Rotating Shadowband Radiometer (MFRSR), and an airborne High Spectral Resolution Lidar (HSRL-2). The average difference (relative to DOAS) for AOD430 is +0.012 ± 0.023 (CIMEL), -0.012 ± 0.024 (MFRSR), -0.011 ± 0.014 (HSRL-2), and +0.023 ± 0.013 (CIMELAOD - MFRSRAOD) and yields the following expressions for correlations between different instruments

  6. Volcanic Aerosol Radiative Properties

    NASA Technical Reports Server (NTRS)

    Lacis, Andrew

    2015-01-01

    Large sporadic volcanic eruptions inject large amounts of sulfur bearing gases into the stratosphere which then get photochemically converted to sulfuric acid aerosol droplets that exert a radiative cooling effect on the global climate system lasting for several years.

  7. The Effect of Aerosol Hygroscopicity and Volatility on Aerosol Optical Properties During Southern Oxidant and Aerosol Study

    NASA Astrophysics Data System (ADS)

    Khlystov, A.; Grieshop, A. P.; Saha, P.; Subramanian, R.

    2014-12-01

    Secondary organic aerosol (SOA) from biogenic sources can influence optical properties of ambient aerosol by altering its hygroscopicity and contributing to light absorption directly via formation of brown carbon and indirectly by enhancing light absorption by black carbon ("lensing effect"). The magnitude of these effects remains highly uncertain. A set of state-of-the-art instruments was deployed at the SEARCH site near Centerville, AL during the Southern Oxidant and Aerosol Study (SOAS) campaign in summer 2013 to measure the effect of relative humidity and temperature on aerosol size distribution, composition and optical properties. Light scattering and absorption by temperature- and humidity-conditioned aerosols was measured using three photo-acoustic extinctiometers (PAX) at three wavelengths (405 nm, 532 nm, and 870 nm). The sample-conditioning system provided measurements at ambient RH, 10%RH ("dry"), 85%RH ("wet"), and 200 C ("TD"). In parallel to these measurements, a long residence time temperature-stepping thermodenuder (TD) and a variable residence time constant temperature TD in combination with three SMPS systems and an Aerosol Chemical Speciation Monitor (ACSM) were used to assess aerosol volatility and kinetics of aerosol evaporation. We will present results of the on-going analysis of the collected data set. We will show that both temperature and relative humidity have a strong effect on aerosol optical properties. SOA appears to increase aerosol light absorption by about 10%. TD measurements suggest that aerosol equilibrated fairly quickly, within 2 s. Evaporation varied substantially with ambient aerosol loading and composition and meteorology.

  8. Microphysical and Chemical Properties of Agricultural Aerosols

    NASA Astrophysics Data System (ADS)

    Brooks, S. D.; Moon, S.; Littleton, R.; Auvermann, B.

    2005-12-01

    Due to significant atmospheric loadings of agricultural dust aerosols, the aerosol's ability to contribute significantly to climate forcing on a regional to global level has been a topic of recent interest. Efforts have been made to quantify both the aerosol extinction of the total aerosol population and the hygroscopic and chemical properties of individual particles at a cattle feedyard near Canyon, Texas. Measurements of aerosol extinction are made using open-path transmissometry. Our results show that extinction varies significantly with relative humidity. To further explore the hygroscopic nature of the particles, size-resolved aerosol samples are collected using a cascade impactor system (7 stages ranging from 0.6 micron to 16 micron diameter) and hygroscopicity measurements are conducted on these using an Environmental Scanning Electron Microscope (ESEM). Complimentary determination of the elemental composition of individual particles is performed using Energy Dispersive X-ray Spectroscopy. Results of the optical properties, hygroscopicity and chemical composition of aerosols will be presented and atmospheric implications discussed.

  9. Deriving simple empirical relationships between aerodynamic and optical aerosol measurements and their application

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Different measurement techniques for aerosol characterization and quantification either directly or indirectly measure different aerosol properties (i.e. count, mass, speciation, etc.). Comparisons and combinations of multiple measurement techniques sampling the same aerosol can provide insight into...

  10. Aerosol optical properties over the Svalbard region of Arctic: ground-based measurements and satellite remote sensing

    NASA Astrophysics Data System (ADS)

    Gogoi, Mukunda M.; Babu, S. Suresh

    2016-05-01

    In view of the increasing anthropogenic presence and influence of aerosols in the northern polar regions, long-term continuous measurements of aerosol optical parameters have been investigated over the Svalbard region of Norwegian Arctic (Ny-Ålesund, 79°N, 12°E, 8 m ASL). This study has shown a consistent enhancement in the aerosol scattering and absorption coefficients during spring. The relative dominance of absorbing aerosols is more near the surface (lower single scattering albedo), compared to that at the higher altitude. This is indicative of the presence of local anthropogenic activities. In addition, long-range transported biomass burning aerosols (inferred from the spectral variation of absorption coefficient) also contribute significantly to the higher aerosol absorption in the Arctic spring. Aerosol optical depth (AOD) estimates from ground based Microtop sun-photometer measurements reveals that the columnar abundance of aerosols reaches the peak during spring season. Comparison of AODs between ground based and satellite remote sensing indicates that deep blue algorithm of Moderate Resolution Imaging Spectroradiometer (MODIS) retrievals over Arctic snow surfaces overestimate the columnar AOD.

  11. Measurements of physical and chemical properties of urban aerosols and their CCN activities in Seoul during the KORUS-AQ pre-campaign

    NASA Astrophysics Data System (ADS)

    Kim, N.; Yum, S. S.; Park, M.; Shin, H. J.; Bae, G. N.; Kwak, K. H.; Park, J. S.; Park, S. M.; Ahn, J.

    2015-12-01

    Interest in cloud condensation nuclei (CCN) has been increasing for the last few decades due to their first order effects on radiative and microphysical properties of clouds. Particularly, scientific understanding of CCN from anthropogenic sources becomes important because it is now considered that large uncertainties in climate change predictions stem from insufficient understanding of CCN. CCN activity is influenced by size and chemical component of aerosols. The KORUS-AQ campaign, jointly organized by National Institute of Environmental Research (NIER) of Korea and National Aeronautics and Space Administration (NASA) aims at understanding various aspects of air quality problem in Korea and will be held in spring, 2016. In preparation for this campaign, pre-campaign was held during May 18-June 13, 2015, in Seoul where numerous local anthropogenic sources exist and influence of Chinese continental outflow directly affects. Here we present some of the important results from the pre-campaign. Chemical properties of aerosols were measured with AMS. Aerosol and CCN number concentrations, aerosol size distribution and aerosol hygroscopic growth factor were measured by CPC, CCN counter, SMPS and H-TDMA, respectively. Average diurnal variation of aerosol number concentration showed three dominant peaks at around 0600_UTC and morning and evening rush hours. Each peak seemed to have different characteristics and therefore detailed analyses of physical and chemical properties of aerosols during the peaks as well as during some special events will be made. The hygroscopicity parameter, kappa, will be estimated by examining CCN activity, H-TDMA measured hygroscopic growth factor and mixing rule of aerosol chemical components, and the result will be compared as well.

  12. Aqueous aerosol SOA formation: impact on aerosol physical properties.

    PubMed

    Woo, Joseph L; Kim, Derek D; Schwier, Allison N; Li, Ruizhi; McNeill, V Faye

    2013-01-01

    Organic chemistry in aerosol water has recently been recognized as a potentially important source of secondary organic aerosol (SOA) material. This SOA material may be surface-active, therefore potentially affecting aerosol heterogeneous activity, ice nucleation, and CCN activity. Aqueous aerosol chemistry has also been shown to be a potential source of light-absorbing products ("brown carbon"). We present results on the formation of secondary organic aerosol material in aerosol water and the associated changes in aerosol physical properties from GAMMA (Gas-Aerosol Model for Mechanism Analysis), a photochemical box model with coupled gas and detailed aqueous aerosol chemistry. The detailed aerosol composition output from GAMMA was coupled with two recently developed modules for predicting a) aerosol surface tension and b) the UV-Vis absorption spectrum of the aerosol, based on our previous laboratory observations. The simulation results suggest that the formation of oligomers and organic acids in bulk aerosol water is unlikely to perturb aerosol surface tension significantly. Isoprene-derived organosulfates are formed in high concentrations in acidic aerosols under low-NO(x) conditions, but more experimental data are needed before the potential impact of these species on aerosol surface tension may be evaluated. Adsorption of surfactants from the gas phase may further suppress aerosol surface tension. Light absorption by aqueous aerosol SOA material is driven by dark glyoxal chemistry and is highest under high-NO(x) conditions, at high relative humidity, in the early morning hours. The wavelength dependence of the predicted absorption spectra is comparable to field observations and the predicted mass absorption efficiencies suggest that aqueous aerosol chemistry can be a significant source of aerosol brown carbon under urban conditions. PMID:24601011

  13. Exploring Divergent Volatility Properties from Yield and Thermodenuder Measurements of Secondary Organic Aerosol from α-Pinene Ozonolysis.

    PubMed

    Saha, Provat K; Grieshop, Andrew P

    2016-06-01

    There are large uncertainties in the parameters dictating the gas-particle partitioning of secondary organic aerosols (SOA), although this process has major influences on their atmospheric lifecycle. Here, we extract parameters that describe the partitioning of SOA from α-pinene ozonolysis using measurements from a dual-thermodenuder (TD) system that constrains both the equilibrium and the kinetic properties that dictate SOA phase partitioning. Parallel TDs that vary in temperature and residence time were used with an evaporation-kinetics model to extract parameter values. An evaporation coefficient of an order of 0.1 best describes the observed evaporation, suggesting equilibration time scales of atmospheric SOA on the order of minutes to hours. A total of 20-40% of SOA mass consists of low-volatility material (saturation concentration of <0.3 μg m(-3)) in the TD-derived SOA volatility distribution. While distinct from existing parametrizations from aerosol growth experiments, derived values are consistent with recent observations of slow room-temperature evaporation of SOA and contributions from extremely low volatility organic compounds formed during α-pinene ozonolysis. The volatility parameters thus determined suggest that SOA yields and enthalpies of evaporation are substantially higher, and products less volatile, than is currently assumed in atmospheric models. These results will help improve the representation of SOA in air-quality and climate models. PMID:27144815

  14. New Approaches to Aerosol Optical Extinction Measurement

    NASA Astrophysics Data System (ADS)

    Strawa, A. W.; Owano, T.; Moosmuller, H.; Atkinson, D.; Covert, D.; Ahlquist, N.; Schmid, B.

    2002-12-01

    Aerosols can have important influences on climate and the radiation balance of the atmosphere. However, the temporal and spatial variability of aerosols and our inadequate knowledge of aerosol optical properties have lead to large uncertainties in these effects. Thus improved in-situ measurements of aerosol optical properties, in particular measurement of their extinction coefficients, are required. Recently, the relatively new technique of cavity ring-down spectroscopy has been applied to the problem of making fast, accurate measurements of aerosol extinction coefficient. Typically, extinction measurements have been made by measuring the decrease in the intensity of a light beam that has passed through a particulate-laden cell. Often, the cell contains mirrors which reflect the beam several times increasing the optical path length thereby increasing the extinction. Path lengths of up to 400 m have been obtained, which is still insufficient to measure atmospheric extinction in the visible down to background values. In cavity ring-down, a light beam is reflected many thousands of times between two highly reflective mirrors, resulting in a path length of kilometers. The light exiting the cell decreases exponentially with time, and this exponential decay is related to the extinction of the aerosol inside the cell. The CRD instruments can routinely measure sub-Rayleigh equivalent extinction levels of a few Mm-^1 and are generally more rugged and portable than traditional extinction cells. Possible applications of CRD-based extinction cells include studies of visibility, climate forcing by aerosol, and the validation of aerosol retrieval schemes from satellites such as MODIS, MISR, and CALYPSO. This paper will present the motivation for making improved aerosol extinction measurements and discuss the problems in making the measurement. The cavity ring-down technique will be described. In June, 2002, a calibration and methods intercomparison, the Reno Aerosol Optics Study

  15. Atmospheric Aerosol Properties and Climate Impacts

    NASA Technical Reports Server (NTRS)

    Chin, Mian; Kahn, Ralph A.; Remer, Lorraine A.; Yu, Hongbin; Rind, David; Feingold, Graham; Quinn, Patricia K.; Schwartz, Stephen E.; Streets, David G.; DeCola, Phillip; Halthore, Rangasayi

    2009-01-01

    This report critically reviews current knowledge about global distributions and properties of atmospheric aerosols, as they relate to aerosol impacts on climate. It assesses possible next steps aimed at substantially reducing uncertainties in aerosol radiative forcing estimates. Current measurement techniques and modeling approaches are summarized, providing context. As a part of the Synthesis and Assessment Product in the Climate Change Science Program, this assessment builds upon recent related assessments, including the Fourth Assessment Report of the Intergovernmental Panel on Climate Change (IPCC AR4, 2007) and other Climate Change Science Program reports. The objectives of this report are (1) to promote a consensus about the knowledge base for climate change decision support, and (2) to provide a synthesis and integration of the current knowledge of the climate-relevant impacts of anthropogenic aerosols for policy makers, policy analysts, and general public, both within and outside the U.S government and worldwide.

  16. Holistic aerosol evaluation using synthesized aerosol aircraft measurements

    NASA Astrophysics Data System (ADS)

    Watson-Parris, Duncan; Reddington, Carly; Schutgens, Nick; Stier, Philip; Carslaw, Ken; Liu, Dantong; Allan, James; Coe, Hugh

    2016-04-01

    Despite ongoing efforts there are still large uncertainties in aerosol concentrations and loadings across many commonly used GCMs. This in turn leads to large uncertainties in the contributions of the direct and indirect aerosol forcing on climate. However, constraining these fields using earth observation data, although providing global coverage, is problematic for many reasons, including the large uncertainties in retrieving aerosol loadings. Additionally, the inability to retrieve aerosols in or around cloudy scenes leads to further sampling biases (Gryspeerdt 2015). Many in-situ studies have used regional datasets to attempt to evaluate the model uncertainties, but these are unable to provide an assessment of the models ability to represent aerosols properties on a global scale. Within the Global Aerosol Synthesis and Science Project (GASSP) we have assembled the largest collection of quality controlled, in-situ aircraft observations ever synthesized to a consistent format. This provides a global set of in-situ measurements of Cloud Condensation Nuclei (CCN) and Black Carbon (BC), amongst others. In particular, the large number of vertical profiles provided by this aircraft data allows us to investigate the vertical structure of aerosols across a wide range of regions and environments. These vertical distributions are particularly valuable when investigating the dominant processes above or below clouds where remote sensing data is not available. Here we present initial process-based assessments of the BC lifetimes and vertical distributions of CCN in the HadGEM-UKCA and ECHAM-HAM models using this data. We use point-by-point based comparisons to avoid the sampling issues associated with comparing spatio-temporal aggregations.

  17. Survey of aerosol optical properties measured as a function of wavelength with multiple photoacoustic instruments in Sacramento during the CARES campaign

    NASA Astrophysics Data System (ADS)

    Dubey, M. K.; Flowers, B. A.; Arnott, W. P.; Mazzoleni, C.; Lack, D. A.; Gyawali, M. S.; Gorkowski, K.; Fast, J. D.; Zaveri, R. A.; Hubbe, J.; Aiken, A. C.

    2010-12-01

    The goal of the Carbonaceous Aerosols and Radiative Effects Study (CARES) in Central California was to develop scientific knowledge on the life cycle of black carbon and organic aerosols in a mixed urban and forested region. The focus was to improve mechanisms by which carbonaceous aerosols are produced and modified and how they alter their optical properties. To achieve this we deployed ten photoacoustic instruments at ground sites (T0 in Sacramento, and T1 in Cool) and on aircraft (DOE-G1 and NOAA-P3) to measure aerosol absorption and scattering as a function of wavelength. Optical properties were measured at 1064, 871, 780, 532, 405, 375 and 355 nm. Analysis of optical properties over this wide spectral range is being used to attribute the contributions of black, brown and organic carbon as it mixes with other aerosol constituents. Diurnal variations of optical properties measured at T0 reflect urban sources while those at T1 are influenced by local biogenic emissions mixed with transported urban emissions. We present optical evidence of particle nucleation and secondary organic formation at the ground sites. Airborne observations on the G-1 are used to gain a regional perspective and also test for self-consistency and/or performances of instruments. We focus on the inter-comparison flight on 18th June, 2010 where photoacoustic data from the NOAA-P3 (Calnex) and G-1 instruments are compared. Our data are combined with measurements of tracers (e.g. CO 2 and CO) and output from WRF-models to gain a predictive understanding of radiative forcing by carbonaceous aerosols in a mixed urban and forested regime.

  18. Toward Creating A Global Retrospective Climatology of Aerosol Properties

    NASA Technical Reports Server (NTRS)

    Curran, Robert J.; Mishchenko, Michael I.; Hansen, James E. (Technical Monitor)

    2000-01-01

    Tropospheric aerosols are thought to cause a significant direct and indirect climate forcing, but the magnitude of this forcing remains highly uncertain because of poor knowledge of global aerosol characteristics and their temporal changes. The standard long-term global product, the one-channel Advanced Very-High-Resolution Radiometer (AVHRR) aerosol optical thickness over the ocean, relies on a single predefined aerosol model and can be inaccurate in many cases. Furthermore, it provides no information on aerosol column number density, thus making it impossible to estimate the indirect aerosol effect on climate. Total Ozone Mapping Spectrometer (TOMS) data can be used to detect absorbing aerosols over land, but are insensitive to aerosols located below one kilometer. It is thus clear that innovative approaches must be employed in order to extract a more quantitative and accurate aerosol climatology from available satellite and other measurements, thus enabling more reliable estimates of the direct and indirect aerosol forcings. The Global Aerosol Climatology Project (GACP) was established in 1998 as part of the Global Energy and Water Cycle Experiment (GEWEX). Its main objective is to analyze satellite radiance measurements and field observations to infer the global distribution of aerosols, their properties, and their seasonal and interannual variations. The overall goal is to develop advanced global aerosol climatologies for the period of satellite data and to make the aerosol climatologies broadly available through the GACP web site.

  19. Investigating aerosol properties in Peninsular Malaysia via the synergy of satellite remote sensing and ground-based measurements

    NASA Astrophysics Data System (ADS)

    Kanniah, Kasturi Devi; Lim, Hui Qi; Kaskaoutis, Dimitris G.; Cracknell, Arthur P.

    2014-03-01

    Spatio-temporal variation and trends in atmospheric aerosols as well as their impact on solar radiation and clouds are crucial for regional and global climate change assessment. These topics are not so well-documented over Malaysia, the fact that it receives considerable amounts of pollutants from both local and trans-boundary sources. The present study aims to analyse the spatio-temporal evolution and decadal trend of Aerosol Optical Depth (AOD) from Terra and Aqua MODIS sensors, to identify different types and origin of aerosols and explore the link between aerosols and solar radiation. AOD and fine-mode fraction (FMF) products from MODIS, AOD and Ångström Exponent (AE) values from AERONET stations along with ground-based PM10 measurements and solar radiation recordings at selected sites in Peninsular Malaysia are used for this scope. The MODIS AODs exhibit a wide spatio-temporal variation over Peninsular Malaysia, while Aqua AOD is consistently lower than that from Terra. The AOD shows a neutral-to-declining trend during the 2000s (Terra satellite), while that from Aqua exhibits an increasing trend (~ 0.01 per year). AERONET AODs exhibit either insignificant diurnal variation or higher values during the afternoon, while their short-term availability does not allow for a trend analysis. Moreover, the PM10 concentrations exhibit a general increasing trend over the examined locations. The sources and destination of aerosols are identified via the HYSPLIT trajectory model, revealing that aerosols during the dry season (June to September) are mainly originated from the west and southwest (Sumatra, Indonesia), while in the wet season (November to March) they are mostly associated with the northeast monsoon winds from the southern China Sea. Different aerosol types are identified via the relationship of AOD with FMF, revealing that the urban and biomass-burning aerosols are the most abundant over the region contributing to a significant reduction (~- 0.21 MJ m- 2) of

  20. Laboratory measurements of the angular light-scattering properties of internally mixed organic and sea-salt aerosol particles using polar nephelometry

    NASA Astrophysics Data System (ADS)

    Curtis, D. B.; Tinilau, S. S.

    2013-12-01

    Aerosol particles play an important, but relatively poorly understood, role in Earth's climate. Sea-salt aerosol is one of the most prevalent naturally occurring aerosols and is therefore expected to have a large effect on climate by scattering incoming solar radiation back to space. While sea-salt aerosol has been thought to be mainly composed of sodium chloride and other salts, measurements have shown the presence of biogenic organic compounds, such as glucose, in primary sea-salt aerosol particles. In addition, the sea-salt aerosol particles can become coated by secondary organics from anthropogenic activities. In order to better understand the potential climate effects of internally mixed organic and sea-salt particles, the angular scattering properties of laboratory-generated aerosols were measured at a wavelength of 532 nm using polar nephelometry. The polar nephelometer collected scattered light with an elliptical mirror and focused it across a linear CCD detector. The instrument was therefore capable of measuring the scattering intensity as a function of scattering angle (the phase function). Two incident polarizations were studied, parallel and perpendicular to the scattering plane, which were then used to calculate the degree of linear polarization. The scattering measurements along with size distribution measurements were used to retrieve the refractive index of the particles by comparison with Mie theory. Particles were generated from solutions of sodium chloride with varying concentrations of organics such as glucose and oxalic acid. In addition, particles generated from authentic sea-water were studied for comparison. Preliminary results indicate that the effective refractive indices of the mixed particles differ significantly from pure sodium chloride and do not follow simple mixing rules used to calculate refractive index from individual components.

  1. Wavelength-Dependent Optical Absorption Properties of Artificial and Atmospheric Aerosol Measured by a Multi-Wavelength Photoacoustic Spectrometer

    NASA Astrophysics Data System (ADS)

    Utry, N.; Ajtai, T.; Pintér, M.; Bozóki, Z.; Szabó, G.

    2014-12-01

    Various aspects of the photoacoustic (PA) detection method are discussed from the point of view of developing it into a routine tool for measuring the wavelength-dependent optical absorption coefficient of artificial and atmospheric aerosol. The discussion includes the issues of calibration, cross-sensitivity to gaseous molecules, background PA signal subtraction, and size-dependent particle losses within the PA system. The results in this paper are based on a recently developed four-wavelength PA system, which has operational wavelengths in the near-infrared, in the visible, and in the ultraviolet. The measured spectra of artificial and atmospheric aerosol prove the outstanding applicability of the presented PA system.

  2. Satellite measurements of tropospheric aerosols

    NASA Technical Reports Server (NTRS)

    Griggs, M.

    1981-01-01

    This investigation uses LANDSAT 2 radiance data and ground-truth measurements of the aerosol optical thickness, obtained previously from five inland sites, to study the usefulness and limitations of the near infrared radiance over inland bodies of water. The linear relationship between LANDSAT 2 MSS7 and aerosol content found in this study can be used to estimate the aerosol content with a standard deviation of 0.42N. Analysis of the data for MSS6 and MSS7 suggest that the larger uncertainty is mostly due to water turbidity, with little contribution from the adjacency effect. The relationship found is best applied to determine an average aerosol content over a period of time at a given target, or an area average at a given time over several targets close together.

  3. 2D-GMAX-DOAS measurements during TCAP: Comparison with MFRSR, HSRL and simultaneous retrievals of trace gases and aerosol optical properties

    NASA Astrophysics Data System (ADS)

    Ortega, I.; Coburn, S.; Kassianov, E.; Barnard, J.; Berg, L. K.; Hostetler, C. A.; Hair, J. W.; Ferrare, R. A.; Volkamer, R. M.

    2012-12-01

    The two Column Aerosol Project (TCAP) investigates uncertainties in the aerosol direct effect in the northern hemisphere mid-latitudes. The DOE Atmospheric Radiation Measurement (ARM) Mobile Facility (AMF) and Mobile Aerosol Observing System (MAOS) provide an opportunity for 1) atmospheric radiation closure studies, and 2) test retrievals of aerosol optical properties in the presence and absence of clouds. This presentation discusses innovative means to access column information about aerosol optical properties in the lower atmosphere from ground based measurements of solar stray light spectra in the hyperspectral domain, i.e., measurements of the Raman Scattering Probability (RSP, the probability that an observed photon has undergone a rotational Raman scattering event), and oxygen dimer slant column densities (O4 SCD) by means of the University of Colorado 2D scanning ground Multi AXis Differential Optical Absorption Spectroscopy (2D-GMAX-DOAS) instrument that was located at the ARM/MAOS site at Cape Cod, MA. We compare retrievals of aerosol optical properties with those retrieved from the MFRSR and the Cimel Sunphotometer, for case studies in the presence/absence of clouds, and assess the need for atmospheric correction of NO2. 2D-GMAX-DOAS also facilitates a link between the ground-based ARM/MAOS dataset and DoE's G1 aircraft, NASA's King Air aircraft, and NASA's OMI satellite (i.e., NO2 vertical column). Early results that explore these linkages are presented for a case study that combines ground based MFRSR, in-situ observations aboard the G1 aircraft, as well as High Spectral Resolution LIDAR aboard the King Air aircraft.

  4. Black carbon aerosol mixing state, organic aerosols and aerosol optical properties over the United Kingdom

    NASA Astrophysics Data System (ADS)

    McMeeking, G. R.; Morgan, W. T.; Flynn, M.; Highwood, E. J.; Turnbull, K.; Haywood, J.; Coe, H.

    2011-09-01

    Black carbon (BC) aerosols absorb sunlight thereby leading to a positive radiative forcing and a warming of climate and can also impact human health through their impact on the respiratory system. The state of mixing of BC with other aerosol species, particularly the degree of internal/external mixing, has been highlighted as a major uncertainty in assessing its radiative forcing and hence its climate impact, but few in situ observations of mixing state exist. We present airborne single particle soot photometer (SP2) measurements of refractory BC (rBC) mass concentrations and mixing state coupled with aerosol composition and optical properties measured in urban plumes and regional pollution over the United Kingdom. All data were obtained using instrumentation flown on the UK's BAe-146-301 large Atmospheric Research Aircraft (ARA) operated by the Facility for Airborne Atmospheric Measurements (FAAM). We measured sub-micron aerosol composition using an aerosol mass spectrometer (AMS) and used positive matrix factorization to separate hydrocarbon-like (HOA) and oxygenated organic aerosols (OOA). We found a higher number fraction of thickly coated rBC particles in air masses with large OOA relative to HOA, higher ozone-to-nitrogen oxides (NOx) ratios and large concentrations of total sub-micron aerosol mass relative to rBC mass concentrations. The more ozone- and OOA-rich air masses were associated with transport from continental Europe, while plumes from UK cities had higher HOA and NOx and fewer thickly coated rBC particles. We did not observe any significant change in the rBC mass absorption efficiency calculated from rBC mass and light absorption coefficients measured by a particle soot absorption photometer despite observing significant changes in aerosol composition and rBC mixing state. The contributions of light scattering and absorption to total extinction (quantified by the single scattering albedo; SSA) did change for different air masses, with lower SSA

  5. 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.

  6. Airborne Atmospheric Aerosol Measurement System

    NASA Astrophysics Data System (ADS)

    Ahn, K.; Park, Y.; Eun, H.; Lee, H.

    2015-12-01

    It is important to understand the atmospheric aerosols compositions and size distributions since they greatly affect the environment and human health. Particles in the convection layer have been a great concern in global climate changes. To understand these characteristics satellite, aircraft, and radio sonde measurement methods have usually been used. An aircraft aerosol sampling using a filter and/or impactor was the method commonly used (Jay, 2003). However, the flight speed particle sampling had some technical limitations (Hermann, 2001). Moreover, the flight legal limit, altitude, prohibited airspace, flight time, and cost was another demerit. To overcome some of these restrictions, Tethered Balloon Package System (T.B.P.S.) and Recoverable Sonde System(R.S.S.) were developed with a very light optical particle counter (OPC), impactor, and condensation particle counter (CPC). Not only does it collect and measure atmospheric aerosols depending on altitudes, but it also monitors the atmospheric conditions, temperature, humidity, wind velocity, pressure, GPS data, during the measurement (Eun, 2013). In this research, atmospheric aerosol measurement using T.B.P.S. in Ansan area is performed and the measurement results will be presented. The system can also be mounted to an unmanned aerial vehicle (UAV) and create an aerial particle concentration map. Finally, we will present measurement data using Tethered Balloon Package System (T.B.P.S.) and R.S.S (Recoverable Sonde System).

  7. Aerosol direct radiative effect over China estimated with visibility measurements

    NASA Astrophysics Data System (ADS)

    Ye, K.; Lin, J.

    2012-12-01

    As a short-lived climate forcer, aerosols exhibit strong radiative effects that vary significantly across the space and time. Current understanding of the long-term variability of aerosol climate forcings is however very poor due to lack of relevant atmospheric measurements. Historic records for visibility measurements from thousands of ground meteorological stations offer a plausible tool to study the decadal and multi-decadal variability of aerosol radiative effects. As a first step, this study presents a method to estimate aerosol direct radiative effect over China based on visibility data for 2006. Visibility data from about 400 ground stations are converted to near-surface aerosol extinction coefficients, which are converted then to aerosol optical depth (AOD) based on spatially and temporally varying vertical distributions of aerosol optical properties simulated by the widely used chemical transport model GEOS-Chem. The resulting AOD data are consistent with direct measurements from the China Aerosol Remote Sensing Network (CARSNET) and the Aerosol Robotic Network (AERONET) in regions where visibility and AOD measurement sites are close in distance. Next, the visibility-derived AOD data are combined with other aerosol optical properties adopted from GEOS-Chem, cloud data from ground stations and surface albedo data from moderate-resolution imaging spectroradiometer (MODIS) to derive the direct radiative effect, by employing the Santa Barbara DISORT Atmospheric Radiative Transfer model (SBDART). Spatial and monthly variations of aerosol radiative effects are examined.

  8. Chemical Properties of Combustion Aerosols: An Overview

    EPA Science Inventory

    A wide variety of pyrogenic and anthropogenic sources emit fine aerosols to the atmosphere. The physical and chemical properties of these aerosols are of interest due to their influence on climate, human health, and visibility. Aerosol chemical composition is remarkably complex. ...

  9. Electrodynamic balance measurements of thermodynamic, kinetic, and optical aerosol properties inaccessible to bulk methods

    NASA Astrophysics Data System (ADS)

    Steimer, S. S.; Krieger, U. K.; Te, Y.-F.; Lienhard, D. M.; Huisman, A. J.; Luo, B. P.; Ammann, M.; Peter, T.

    2015-06-01

    Measurements of a single, levitated particle in an electrodynamic balance are an established tool for deriving thermodynamic and material data such as density, refractive index and activities of components of an aqueous solution under supersaturated conditions, where bulk measurements are not possible. The retrieval relies on combining mass-to-charge data and size data from light scattering. Here, we use a combination of low- and high-resolution Mie resonance spectroscopy to obtain radius data, enabling an accurate size determination not only when the particle is in equilibrium, but also when it is out of equilibrium due to kinetic limitation of mass transport. With the data measured under non-equilibrium conditions, it is possible to retrieve the water diffusivity. A challenge is that the radius retrieval by comparing measured light scattering with Mie theory requires the knowledge of refractive index as a function of concentration. Here, we show an iterative retrieval of refractive index and size for compounds for which data cannot be obtained in the bulk either due to lack of sufficient amounts of sample or limited solubility. We demonstrate the measurement strategy and the retrieval of water activity, density, refractive index and water diffusivity for aqueous shikimic acid. Water diffusivity in concentrated shikimic acid decreases by 6 orders of magnitude at 250 K compared to that at room temperature.

  10. Electrodynamic balance measurements of thermodynamic, kinetic, and optical aerosol properties inaccessible to bulk methods

    NASA Astrophysics Data System (ADS)

    Steimer, S. S.; Krieger, U. K.; Te, Y.-F.; Lienhard, D. M.; Huisman, A. J.; Ammann, M.; Peter, T.

    2015-01-01

    Measurements of a single, levitated particle in an electrodynamic balance are an established tool for deriving thermodynamic and material data such as density, refractive index and activities of components of an aqueous solution under supersaturated conditions, where bulk measurements are not possible. The retrieval relies on combining mass-to-charge data and size data from light scattering. Here, we use a combination of low- and high-resolution Mie resonance spectroscopy to obtain radius data, enabling an accurate size determination not only when the particle is in equilibrium, but also when it is out of equilibrium due to kinetic limitation of mass transport. With the data measured under non-equilibrium conditions, it is possible to retrieve the water diffusivity. A challenge is that the radius retrieval by comparing measured light scattering with Mie theory requires the knowledge of refractive index as a function of concentration. Here, we show an iterative retrieval of refractive index and size for compounds for which data cannot be obtained in the bulk either due to lack of sufficient amounts of sample or limited solubility. We demonstrate the measurement strategy and the retrieval of water activity, density, refractive index and water diffusivity for aqueous shikimic acid. Water diffusivity in concentrated shikimic acid decreases by 6 orders of magnitude at 250 K compared to that at room temperature.

  11. 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.

  12. Satellite stratospheric aerosol measurement validation

    NASA Technical Reports Server (NTRS)

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

    1984-01-01

    The validity of the stratospheric aerosol measurements made by the satellite sensors SAM II and SAGE was tested by comparing their results with each other and with results obtained by other techniques (lider, dustsonde, filter, and impactor). The latter type of comparison required the development of special techniques that convert the quantity measured by the correlative sensor (e.g., particle backscatter, number, or mass) to that measured by the satellite sensor (extinction) and quantitatively estimate the uncertainty in the conversion process. The results of both types of comparisons show agreement within the measurement and conversion uncertainties. Moreover, the satellite uncertainty is small compared to aerosol natural variability (caused by seasonal changes, volcanoes, sudden warmings, and vortex structure). It was concluded that the satellite measurements are valid.

  13. Satellite stratospheric aerosol measurement validation

    NASA Technical Reports Server (NTRS)

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

    1984-01-01

    The validity of the stratospheric aerosol measurements made by the satellite sensors SAM II and SAGE was tested by comparing their results with each other and with results obtained by other techniques (lider, dustsonde, filter, and impactor). The latter type of comparison required the development of special techniques that convert the quantity measured by the correlative sensor (e.g. particle backscatter, number, or mass) to that measured by the satellite sensor (extinction) and quantitatively estimate the uncertainty in the conversion process. The results of both types of comparisons show agreement within the measurement and conversion uncertainties. Moreover, the satellite uncertainty is small compared to aerosol natural variability (caused by seasonal changes, volcanoes, sudden warmings, and vortex structure). It was concluded that the satellite measurements are valid.

  14. 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.

  15. Aerosol Optical Properties in Southeast Asia From AERONET Observations

    NASA Astrophysics Data System (ADS)

    Eck, T. F.; Holben, B. N.; Boonjawat, J.; Le, H. V.; Schafer, J. S.; Reid, J. S.; Dubovik, O.; Smirnov, A.

    2003-12-01

    There is little published data available on measured optical properties of aerosols in the Southeast Asian region. The AERONET project and collaborators commenced monitoring of aerosol optical properties in February 2003 at four sites in Thailand and two sites in Viet Nam to measure the primarily anthropogenic aerosols generated by biomass burning and fossil fuel combustion/ industrial emissions. Automatic sun/sky radiometers at each site measured spectral aerosol optical depth in 7 wavelengths from 340 to 1020 nm and combined with directional radiances in the almucantar, retrievals were made of spectral single scattering albedo and aerosol size distributions. Angstrom exponents, size distributions and spectral single scattering albedo of primarily biomass burning aerosols at rural sites are compared to measurements made at AERONET sites in other major biomass burning regions in tropical southern Africa, South America, and in boreal forest regions. Additionally, the aerosol single scattering albedo and size distributions measured in Bangkok, Thailand are compared with those measured at other urban sites globally. The influences of aerosols originating from other regions outside of Southeast Asia are analyzed using trajectory analyses. Specifically, cases of aerosol transport and mixing from Southern China and from India are presented.

  16. Global Aerosol Effect Retrieval From Passive Hyperspectral Measurements

    NASA Astrophysics Data System (ADS)

    de Graaf, M.; Tilstra, L. G.; Stammes, P.

    2013-12-01

    Absorbing aerosols can have a significant local direct radiative effect (DRE), while the global average aerosol DRE remains highly uncertain. Modelling studies have shown that the magnitude and sign of the aerosol DRE at the top of the atmosphere (TOA) depend on the scene, especially on the albedo of the scene under the aerosol layer. It changes with cloud fraction, from large positive for overcast conditions when aerosols are present above the cloud, to large negative for clear sky ocean scenes. Observational studies, which are necessary to constrain the model studies, have been scarce. The results of modelling studies depend strongly on the assumed aerosol properties. Observational studies also need to assume aerosol type and geophysical properties to derive aerosol optical properties from radiation measurements. This introduces large uncertainties in the retrieved aerosol DRE. Furthermore, the retrieval of aerosols over clouds from passive instruments is difficult, due to the large optical thickness of clouds. Therefore, observational studies of aerosol direct and indirect effects from passive satellite instruments are invariably restricted to aerosol studies close to the cloud edges. We have developed a method to derive the aerosol DRE for smoke over clouds directly from passive satellite hyperspectral reflectance measurements, independent of aerosol micro- physical property assumptions. This allows us to assess the local aerosol DRE from passive imagery directly on a pixel to pixel basis, even over clouds. The solar radiative absorption by smoke layers is quantified using the TOA reflectance spectrum from the ultraviolet (UV) to the shortwave infrared (SWIR). UV- absorbing aerosols have a strong signature that can be detected using UV reflectance measurements. Since the aerosol extinction optical thickness decreases rapidly with increasing wavelength for smoke, the properties of the scene below the aerosol layer can be retrieved in the SWIR, where aerosol

  17. Field and laboratory measurements of cloud-forming properties of combustion aerosols

    SciTech Connect

    Hudson, J.G.; Hallett, J.; Rogers, C.F. )

    1991-06-20

    Measurements of condensation nuclei (CN) and cloud condensation nuclei (CCN) were obtained from aircraft penetrations of controlled burns of chaparral, pine forest, and a JP-4 (jet fuel) pool fire. Vegetative burns gave rise to large numbers of CN, most of which were also CCN at a supersaturation of less than 1%. This is to be contrasted with the much lower activity of smoke from JP-4 burns which gave only 1--2% CCN activity under identical conditions. The field observations are consistent with laboratory results under conditions which simulate natural clouds. This implies that although droplets readily grow on smoke from vegetative burns leading to activation of a significant number of the particles, mutual competition ensures that a large number of interstitial haze particles remain. By contrast, in clouds produced from smoke from jet fuel combustion, a larger fraction of the nonactive interstitial particles remain after cloud formation. Penetrations of a forest fire capping cloud show high concentrations ({gt}10{sup 4} cm{sup {minus}3}) of small (2 {mu}m diameter) but optically active particles together with high concentrations (5{times}10{sup 5} cm{sup {minus}3}) of nonactivated haze particles. Photogrammetric measurements of vertical velocities of clouds from controlled burns showed that weakly sheared plumes penetrated upward more effectively than strongly sheared plumes with cloud and smoke cap velocities as large as 20 m s{sup {minus}1}. This implies vertical velocities twice this value and cloud supersaturations of {similar to}2% under the observation conditions. Implications for particle removal by in-cloud scavenging and precipitation are discussed. {copyright} American Geophysical Union 1991

  18. Statistical characteristics of atmospheric aerosol as determined from AERONET measurements

    NASA Astrophysics Data System (ADS)

    Yoon, Jongmin; Kokhanovsky, Alexander

    2015-04-01

    Seasonal means and standard deviations of column-integrated aerosol optical properties (e.g. spectral aerosol optical thickness (AOT), single scattering albedo, phase function, Ångström exponent, volume particle size distribution, complex refractive index, absorbing aerosol optical thickness) from several Aerosol Robotic Network (AERONET) sites located in typical aerosol source and background regions are investigated (Holben et al., 1998). The AERONET program is an inclusive network of ground-based sun-photometers that measure atmospheric aerosol optical properties (http://aeronet.gsfc.nasa.gov/). The results can be used for improving the accuracy of satellite-retrieved AOT, assessments of the global aerosol models, studies of atmospheric pollution and aerosol radiative forcing on climate. We have paid a special attention to several AERONET sites that are Mexico_City (Mexico), Alta_Floresta (Brazil), Avignon (France), Solar_Village (Saudi Arabia), and Midway_Island (Pacific) representative for industrial/urban, biomass burning, rural, desert dust and oceanic aerosols, respectively. We have found that the optical and microphysical aerosol properties are highly dependent on the local aerosol emission sources and seasonal meteorological conditions.

  19. 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

  20. 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

  1. Aerosol Absorption Measurements in MILAGRO.

    NASA Astrophysics Data System (ADS)

    Gaffney, J. S.; Marley, N. A.; Arnott, W. P.; Paredes-Miranda, L.; Barnard, J. C.

    2007-12-01

    During the month of March 2006, a number of instruments were used to determine the absorption characteristics of aerosols found in the Mexico City Megacity and nearby Valley of Mexico. These measurements were taken as part of the Department of Energy's Megacity Aerosol Experiment - Mexico City (MAX-Mex) that was carried out in collaboration with the Megacity Interactions: Local and Global Research Observations (MILAGRO) campaign. MILAGRO was a joint effort between the DOE, NSF, NASA, and Mexican agencies aimed at understanding the impacts of a megacity on the urban and regional scale. A super-site was operated at the Instituto Mexicano de Petroleo in Mexico City (designated T-0) and at the Universidad Technologica de Tecamac (designated T-1) that was located about 35 km to the north east of the T-0 site in the State of Mexico. A third site was located at a private rancho in the State of Hidalgo approximately another 35 km to the northeast (designated T-2). Aerosol absorption measurements were taken in real time using a number of instruments at the T-0 and T-1 sites. These included a seven wavelength aethalometer, a multi-angle absorption photometer (MAAP), and a photo-acoustic spectrometer. Aerosol absorption was also derived from spectral radiometers including a multi-filter rotating band spectral radiometer (MFRSR). The results clearly indicate that there is significant aerosol absorption by the aerosols in the Mexico City megacity region. The absorption can lead to single scattering albedo reduction leading to values below 0.5 under some circumstances. The absorption is also found to deviate from that expected for a "well-behaved" soot anticipated from diesel engine emissions, i.e. from a simple 1/lambda wavelength dependence for absorption. Indeed, enhanced absorption is seen in the region of 300-450 nm in many cases, particularly in the afternoon periods indicating that secondary organic aerosols are contributing to the aerosol absorption. This is likely due

  2. Aerosol optical properties in the Iranian region obtained by ground-based solar radiation measurements in the summer of 1991

    SciTech Connect

    Nakajima, Teruyuki; Hayasaka, Tadahiro; Higurashi, Akiko; Hashida, Gen; Moharram-Nejad, N.; Najafi, Y.; Valavi, H.

    1996-08-01

    Solar radiation measurements were made using sun photometers and pyranometers during 31 May-7 June 1991 at several places in Iran and during 12 June-17 September 1991 at a fixed place, Bushehr, Iran. In the first period the aerosol optical thickness had values about 0.4 at the wavelength of 0.5 {mu}m in the coastal area and about 0.2 in the plateau area. The Angstrom`s exponent, which is the slope of optical thickness spectrum, had values around 1 for large city areas and less than 0.5 for inland arid areas. Chemical analyses of sampled air indicate an effect of fossil fuel burning from local sources. Such optical and chemical characteristics of atmospheres suggest that soil-derived coarse particles contributed considerably to the atmospheric turbidity in arid areas, whereas an active generation of aerosols was dominant near large cities. Significant rises in atmospheric turbidity were observed in the earlier part of the second period at Bushehr about once a week with a duration of about one day, which may have been caused by smoke from oil-well fires in Kuwait. The aerosol optical thickness in these events had values of about 1.5, which is equivalent to a columnar aerosol volume of 4.4 x 10{sup -4} cm{sup 3} cm{sup -2}. The absorption index ranged from 0.005 to 0.02 with several peaks reaching 0.1 in the second period. These peaks can be attributed to prevailing smoke particles. 32 refs., 15 figs., 3 tabs.

  3. Climatology of Aerosol Optical Properties in Southern Africa

    NASA Technical Reports Server (NTRS)

    Queface, Antonio J.; Piketh, Stuart J.; Eck, Thomas F.; Tsay, Si-Chee

    2011-01-01

    A thorough regionally dependent understanding of optical properties of aerosols and their spatial and temporal distribution is required before we can accurately evaluate aerosol effects in the climate system. Long term measurements of aerosol optical depth, Angstrom exponent and retrieved single scattering albedo and size distribution, were analyzed and compiled into an aerosol optical properties climatology for southern Africa. Monitoring of aerosol parameters have been made by the AERONET program since the middle of the last decade in southern Africa. This valuable information provided an opportunity for understanding how aerosols of different types influence the regional radiation budget. Two long term sites, Mongu in Zambia and Skukuza in South Africa formed the core sources of data in this study. Results show that seasonal variation of aerosol optical thicknesses at 500 nm in southern Africa are characterized by low seasonal multi-month mean values (0.11 to 0.17) from December to May, medium values (0.20 to 0.27) between June and August, and high to very high values (0.30 to 0.46) during September to November. The spatial distribution of aerosol loadings shows that the north has high magnitudes than the south in the biomass burning season and the opposite in none biomass burning season. From the present aerosol data, no long term discernable trends are observable in aerosol concentrations in this region. This study also reveals that biomass burning aerosols contribute the bulk of the aerosol loading in August-October. Therefore if biomass burning could be controlled, southern Africa will experience a significant reduction in total atmospheric aerosol loading. In addition to that, aerosol volume size distribution is characterized by low concentrations in the non biomass burning period and well balanced particle size contributions of both coarse and fine modes. In contrast high concentrations are characteristic of biomass burning period, combined with

  4. Identification of aerosol composition from multi-wavelength lidar measurements

    NASA Technical Reports Server (NTRS)

    Wood, S. A.

    1984-01-01

    This paper seeks to develop the potential of lidar for the identification of the chemical composition of atmospheric aerosols. Available numerical computations suggest that aerosols can be identified by the wavelength dependence of aerosol optical properties. Since lidar can derive the volume backscatter coefficient as a function of wavelength, a multi-wavelength lidar system may be able to provide valuable information on the composition of aerosols. This research theoretically investigates the volume backscatter coefficients for the aerosol classes, sea-salts, and sulfates, as a function of wavelength. The results show that these aerosol compositions can be characterized and identified by their backscatter wavelength dependence. A method to utilize multi-wavelength lidar measurements to discriminate between compositionally different thin aerosol layers is discussed.

  5. Column Aerosol Optical Properties and Aerosol Radiative Forcing During a Serious Haze-Fog Month over North China Plain in 2013 Based on Ground-Based Sunphotometer Measurements

    NASA Technical Reports Server (NTRS)

    Che, H.; Xia, X.; Zhu, J.; Li, Z.; Dubovik, O.; Holben, Brent N.; Goloub, P.; Chen, H.; Estelles, V.; Cuevas-Agullo, E.

    2014-01-01

    In January 2013, North China Plain experienced several serious haze events. Cimel sunphotometer measurements at seven sites over rural, suburban and urban regions of North China Plain from 1 to 30 January 2013 were used to further our understanding of spatial-temporal variation of aerosol optical parameters and aerosol radiative forcing (ARF). It was found that Aerosol Optical Depth at 500 nm (AOD500nm) during non-pollution periods at all stations was lower than 0.30 and increased significantly to greater than 1.00 as pollution events developed. The Angstrom exponent (Alpha) was larger than 0.80 for all stations most of the time. AOD500nm averages increased from north to south during both polluted and non-polluted periods on the three urban sites in Beijing. The fine mode AOD during pollution periods is about a factor of 2.5 times larger than that during the non-pollution period at urban sites but a factor of 5.0 at suburban and rural sites. The fine mode fraction of AOD675nm was higher than 80% for all sites during January 2013. The absorption AOD675nm at rural sites was only about 0.01 during pollution periods, while 0.03-0.07 and 0.01-0.03 during pollution and non-pollution periods at other sites, respectively. Single scattering albedo varied between 0.87 and 0.95 during January 2013 over North China Plain. The size distribution showed an obvious tri-peak pattern during the most serious period. The fine mode effective radius in the pollution period was about 0.01-0.08 microns larger than during nonpollution periods, while the coarse mode radius in pollution periods was about 0.06-0.38 microns less than that during nonpollution periods. The total, fine and coarse mode particle volumes varied by about 0.06-0.34 cu microns, 0.03-0.23 cu microns, and 0.03-0.10 cu microns, respectively, throughout January 2013. During the most intense period (1-16 January), ARF at the surface exceeded -50W/sq m, -180W/sq m, and -200W/sq m at rural, suburban, and urban sites

  6. Aerosol properties in Titan's upper atmosphere

    NASA Astrophysics Data System (ADS)

    Lavvas, Panayotis; Koskinen, Tommi; Royer, Emilie; Rannou, Pascal; West, Robert

    2016-06-01

    Multiple Cassini observations reveal that the abundant aerosol particles in Titan's atmosphere are formed at high altitudes, particularly in the thermosphere. They subsequently fall towards the lower atmosphere and in their path their size, shape, and population change in reflection to the variable atmospheric condition. Although multiple observations can help us retrieve information for the aerosol properties in the lower atmosphere, we have limited information for the aerosol properties between their formation region in the thermosphere and the upper region of the main haze layer or the detached aerosol layer. Observations at UV wavelengths are the only way to probe this part of the atmosphere and help us retrieve the aerosol properties. The presentation will provide an overview of the available observations, and discuss their implications for the production and evolution of Titan's aerosols.

  7. An update on polar aerosol optical properties using POLAR-AOD and other measurements performed during the International Polar Year

    NASA Astrophysics Data System (ADS)

    Tomasi, Claudio; Lupi, Angelo; Mazzola, Mauro; Stone, Robert S.; Dutton, Ellsworth G.; Herber, Andreas; Radionov, Vladimir F.; Holben, Brent N.; Sorokin, Mikhail G.; Sakerin, Sergey M.; Terpugova, Svetlana A.; Sobolewski, Piotr S.; Lanconelli, Christian; Petkov, Boyan H.; Busetto, Maurizio; Vitale, Vito

    2012-06-01

    An updated set of time series of derived aerosol optical depth (AOD) and Ångström's exponent α from a number of Arctic and Antarctic stations was analyzed to determine the long-term variations of these two parameters. The Arctic measurements were performed at Ny-Ålesund (1991-2010), Barrow (1977-2010) and some Siberian sites (1981-1991). The data were integrated with Level 2.0 AERONET sun-photometer measurements recorded at Hornsund, Svalbard, and Barrow for recent years, and at Tiksi for the summer 2010. The Antarctic data-set comprises sun-photometer measurements performed at Mirny (1982-2009), Neumayer (1991-2004), and Terra Nova Bay (1987-2005), and at South Pole (1977-2010). Analyses of daily mean AOD were made in the Arctic by (i) adjusting values to eliminate volcanic effects due to the El Chichón, Pinatubo, Kasatochi and Sarychev eruptions, and (ii) selecting the summer background aerosol data from those affected by forest fire smoke. Nearly null values of the long-term variation of summer background AOD were obtained at Ny-Ålesund (1991-2010) and at Barrow (1977-2010). No evidence of important variations in AOD was found when comparing the monthly mean values of AOD measured at Tiksi in summer 2010 with those derived from multi-filter actinometer measurements performed in the late 1980s at some Siberian sites. The long-term variations of seasonal mean AOD for Arctic Haze (AH) conditions and AH episode seasonal frequency were also evaluated, finding that these parameters underwent large fluctuations over the 35-year period at Ny-Ålesund and Barrow, without presenting well-defined long-term variations. A characterization of chemical composition, complex refractive index and single scattering albedo of ground-level aerosol polydispersions in summer and winter-spring is also presented, based on results mainly found in the literature. The long-term variation in Antarctic AOD was estimated to be stable, within ±0.10% per year, at the three coastal sites

  8. Overview of ACE-Asia Spring 2001 Investigations on Aerosol Radiative Effects and Related Aerosol Properties

    NASA Technical Reports Server (NTRS)

    Russell, Philip B.; Valero, F. P. J.; Flatau, P. J.; Bergin, M.; Holben, B.; Nakajima, T.; Pilewskie, P.; Bergstrom, R.; Hipskind, R. Stephen (Technical Monitor)

    2001-01-01

    A primary, ACE-Asia objective was to quantify the interactions between aerosols and radiation in the Asia-Pacific region. Toward this end, radiometric and related aerosol measurements were made from ocean, land, air and space platforms. Models that predict aerosol fields guided the measurements and are helping integrate and interpret results. Companion overview's survey these measurement and modeling components. Here we illustrate how these components were combined to determine aerosol radiative. impacts and their relation to aerosol properties. Because clouds can obscure or change aerosol direct radiative effects, aircraft and ship sorties to measure these effects depended on predicting and finding cloud-free areas and times with interesting aerosols present. Pre-experiment satellite cloud climatologies, pre-flight aerosol and cloud forecasts, and in-flight guidance from satellite imagery all helped achieve this. Assessments of aerosol regional radiative impacts benefit from the spatiotemporal coverage of satellites, provided satellite-retrieved aerosol properties are accurate. Therefore, ACE-Asia included satellite retrieval tests, as part of many comparisons to judge the consistency (closure) among, diverse measurements. Early results include: (1) Solar spectrally resolved and broadband irradiances and optical depth measurements from the C-130 aircraft and at Kosan, Korea yielded aerosol radiative forcing efficiencies, permitting comparisons between efficiencies of ACE-Asia and INDOEX aerosols, and between dust and "pollution" aerosols. Detailed results will be presented in separate papers. (2) Based on measurements of wavelength dependent aerosol optical depth (AOD) and single scattering albedo the estimated 24-h a average aerosol radiative forcing efficiency at the surface for photosynthetically active radiation (400 - 700 nm) in Yulin, China is approx. 30 W sq m per AOD(500 nm). (3) The R/V Brown cruise from Honolulu to Sea of Japan sampled an aerosol optical

  9. An investigation of aerosol optical properties: Atmospheric implications and influences

    NASA Astrophysics Data System (ADS)

    Penaloza-Murillo, Marcos A.

    An experimental, observational, and theoretical investigation of aerosol optical properties has been made in this work to study their implications and influences on the atmosphere. In the laboratory the scientific and instrumental methodology consisted of three parts, namely, aerosol generation, optical and mass concentration measurements, and computational calculations. In particular the optical properties of ammonium sulfate and caffeine aerosol were derived from measurements made with a transmissometer cell-reciprocal- integrating nephelometer (TCRIN), equipped with a laser beam at 632.8 nm, and by applying a Mie theory computer code The aerosol generators, optical equipment and calibration procedures were reviewed. The aerosol shape and size distribution were studied by means of scanning electron microscopy and the Gumprecht- Sliepcevich/Lipofsky-Green extinction-sedimentation method. In particular the spherical and cylindrical shape were considered. During this investigation, an alternative method for obtaining the optical properties of monodisperse spherical non-absorbing aerosol using a cell-transmissometer, which is based on a linearisation of the Lambert-Beer law, was found. In addition, adapting the TCRIN to electrooptical aerosol studies, the optical properties of a circular-cylindrical aerosol of caffeine were undertaken under the condition of random orientation in relation with the laser beam, and perpendicular orientation to it. A theoretical study was conducted to assess the sensitivity of aerosol to a change of shape under different polarisation modes. The aerosol optical properties, obtained previously in the laboratory, were then used to simulate the direct radiative forcing. The calculations and results were obtained by applying a one- dimensional energy-balance box model. The influence of atmospheric aerosol on the sky brightness due to a total solar eclipse was studied using the photometric and meteorological observations made during the

  10. Crowdsourced aerosol measurements using smartphone spectropolarimeters

    NASA Astrophysics Data System (ADS)

    Rietjens, J.; Snik, F.; Keller, C. U.; Heinsbroek, R.; van Harten, G.; Heikamp, S.; de Boer, J.; Zeegers, E.; Einarsen, L.; Hasekamp, O.; Smit, M.; di Noia, A.; Apituley, A.; Mijling, B.; Hendriks, E.; Stammes, P.; Volten, H.; Vonk, J.; Berkhout, S.; Haaima, M.; van der Hoff, R.; Stam, D.; Navarro, R.; Bettonvil, F.

    2013-12-01

    We present the development, organisation and results of a large citizen science project with the goal to measure and characterise atmospheric aerosols using a network of smartphone spectropolarimeters. The project, called ';iSPEX', was conceived and carried out in the Netherlands, and organised the first National iSPEX measurement day on July 8th 2013. During this day, more than 3000 people performed over 6000 measurements with their own smartphones using a special add-on and a dedicated app. These measurements were sent to a central database, processed and analysed using a vector-radiative transfer based inversion code in order to extract aerosol properties. The add-on that transforms the camera of the smartphone into a spectropolarimeter and thereby the smartphone into a scientific instrument, employs the method of spectral modulation [1]. The add-on is comprised of polymer parts and was mass-produced and distributed to almost 10000 people. A single measurement involves scanning the blue sky, thereby yielding the angular behaviour of the degree of linear polarisation as a function of wavelength. Although a single iSPEX measurement is not accurate enough, combining many measurements of a crowdsourced experiment with thousands of people should yield sufficiently accurate results that may be interpreted in terms of aerosol optical thickness and aerosol particle properties. By analysing not only the measured results, but also the motivation of the general public to participate, we learn about the possibilities to create a new kind of air quality measurement network. At the conference, we will demonstrate iSPEX and present the results of the first measurement day. We hope to convince you that iSPEX is not only a great outreach tool to engage the public in issues pertaining to atmospheric aerosols, but that it may also contribute to the solution of several urgent societal and scientific problems. [1] Snik, F., Karalidi, T., Keller, C.U.. Spectral modulation for full

  11. Variability of aerosol properties and Planetary Boundary Layer heights from airborne High Spectral Resolution Lidar, ground-based measurements, and the WRF model during CalNex and CARES

    NASA Astrophysics Data System (ADS)

    Obland, M. D.; Swanson, A. J.; Ferrare, R. A.; Burton, S. P.; Hair, J. W.; Hostetler, C. A.; Rogers, R.; Fast, J. D.; Berg, L. K.; Pekour, M. S.; Shaw, W. J.; Zaveri, R. A.; Haman, C. L.; Cook, A.; Harper, D.

    2011-12-01

    The NASA airborne High Spectral Resolution Lidar (HSRL) was deployed on board the NASA Langley Research Center's B200 aircraft to California in May and June of 2010 to aid in characterizing aerosol properties during the CalNex and CARES field missions. Measurements of aerosol extinction (at 532 nm), backscatter (at 532 and 1064 nm), and depolarization (at 532 and 1064 nm) during 31 flights and nearly 100 hours, many in coordination with other participating research aircraft, satellites, and ground sites, constitute a diverse data set for use in characterizing the spatial and temporal distribution of aerosols, as well as properties and variability of the Planetary Boundary Layer (PBL). This work examines the variability of the extensive (dependent on aerosol type and number density) and intensive (dependent on aerosol type only) aerosol properties to aid in describing the broader context of aerosol behavior within and nearby the Sacramento and Los Angeles Basin regions. PBL heights derived from HSRL measurements will be compared with those produced by local ceilometers, radiosondes, and the Weather Research and Forecasting (WRF) model. Spatial and temporal averages of aerosol properties will be presented.

  12. Vertical structure and optical properties of Titan's aerosols from radiance measurements made inside and outside the atmosphere

    NASA Astrophysics Data System (ADS)

    Doose, Lyn R.; Karkoschka, Erich; Tomasko, Martin G.; Anderson, Carrie M.

    2016-05-01

    Prompted by the detection of stratospheric cloud layers by Cassini's Composite Infrared Spectrometer (CIRS; see Anderson, C.M., Samuelson, R.E. [2011]. Icarus 212, 762-778), we have re-examined the observations made by the Descent Imager/Spectral Radiometer (DISR) in the atmosphere of Titan together with two constraints from measurements made outside the atmosphere. No evidence of thin layers (<1 km) in the DISR image data sets is seen beyond the three previously reported layers at 21 km, 11 km, and 7 km by Karkoschka and Tomasko (Karkoschka, E., Tomasko, M.G. [2009]. Icarus 199, 442-448). On the other hand, there is evidence of a thicker layer centered at about 55 km. A rise in radiance gradients in the Downward-Looking Visible Spectrometer (DLVS) data below 55 km indicates an increase in the volume extinction coefficient near this altitude. To fit the geometric albedo measured from outside the atmosphere the decrease in the single scattering albedo of Titan's aerosols at high altitudes, noted in earlier studies of DISR data, must continue to much higher altitudes. The altitude of Titan's limb as a function of wavelength requires that the scale height of the aerosols decrease with altitude from the 65 km value seen in the DISR observations below 140 km to the 45 km value at higher altitudes. We compared the variation of radiance with nadir angle observed in the DISR images to improve our aerosol model. Our new aerosol model fits the altitude and wavelength variations of the observations at small and intermediate nadir angles but not for large nadir angles, indicating an effect that is not reproduced by our radiative transfer model. The volume extinction profiles are modeled by continuous functions except near the enhancement level near 55 km altitude. The wavelength dependence of the extinction optical depth is similar to earlier results at wavelengths from 500 to 700 nm, but is smaller at shorter wavelengths and larger toward longer wavelengths. A Hapke

  13. A comparative study of aerosol microphysical properties retrieved from ground-based remote sensing and aircraft in situ measurements during a Saharan dust event

    NASA Astrophysics Data System (ADS)

    José Granados-Muñoz, María; Bravo-Aranda, Juan Antonio; Baumgardner, Darrel; Guerrero-Rascado, Juan Luis; Pérez-Ramírez, Daniel; Navas-Guzmán, Francisco; Veselovskii, Igor; Lyamani, Hassan; Valenzuela, Antonio; José Olmo, Francisco; Titos, Gloria; Andrey, Javier; Chaikovsky, Anatoli; Dubovik, Oleg; Gil-Ojeda, Manuel; Alados-Arboledas, Lucas

    2016-03-01

    In this work we present an analysis of aerosol microphysical properties during a mineral dust event taking advantage of the combination of different state-of-the-art retrieval techniques applied to active and passive remote sensing measurements and the evaluation of some of those techniques using independent data acquired from in situ aircraft measurements. Data were collected in a field campaign performed during a mineral dust outbreak at the Granada, Spain, experimental site (37.16° N, 3.61° W, 680 m a.s.l.) on 27 June 2011. Column-integrated properties are provided by sun- and star-photometry, which allows for a continuous evaluation of the mineral dust optical properties during both day and nighttime. Both the linear estimation and AERONET (Aerosol Robotic Network) inversion algorithms are applied for the retrieval of the column-integrated microphysical particle properties. In addition, vertically resolved microphysical properties are obtained from a multi-wavelength Raman lidar system included in EARLINET (European Aerosol Research Lidar Network), by using both LIRIC (Lidar Radiometer Inversion Code) algorithm during daytime and an algorithm applied to the Raman measurements based on the regularization technique during nighttime. LIRIC retrievals reveal the presence of dust layers between 3 and 5 km a.s.l. with volume concentrations of the coarse spheroid mode up to 60 µm3 cm-3. The combined use of the regularization and LIRIC methods reveals the night-to-day evolution of the vertical structure of the mineral dust microphysical properties and offers complementary information to that from column-integrated variables retrieved from passive remote sensing. Additionally, lidar depolarization profiles and LIRIC retrieved volume concentration are compared with aircraft in situ measurements. This study presents for the first time a comparison of the total volume concentration retrieved with LIRIC with independent in situ measurements, obtaining agreement within

  14. Aerosol activation properties and CCN closure during TCAP

    NASA Astrophysics Data System (ADS)

    Mei, F.; Tomlinson, J. M.; Shilling, J. E.; Wilson, J. M.; Zelenyuk, A.; Chand, D.; Comstock, J. M.; Hubbe, J.; Berg, L. K.; Schmid, B.

    2013-12-01

    The indirect effects of atmospheric aerosols currently remain the most uncertain components in forcing of climate change over the industrial period (IPCC, 2007). This large uncertainty is partially due to our incomplete understanding of the ability of particles to form cloud droplets under atmospherically relevant supersaturation. In addition, there is a large uncertainty in the aerosol optical depth (AOD) simulated by climate models near the North American coast and a wide variety in the types of clouds are observed over this region. The goal of the US Department of Energy Two Column Aerosol Project (TCAP) is to understand the processes responsible for producing and maintaining aerosol distributions and associated radiative and cloud forcing off the coast of North America. During the TCAP study, aerosol total number concentration, cloud condensation nuclei (CCN) spectra and aerosol chemical composition were in-situ measured from the DOE Gulfstream 1 (G-1) research aircraft during two Intensive Operations Periods (IOPs), one conducted in July 2012 and the other in February 2013. An overall aerosol size distribution was achieved by merging the observations from several instruments, including Ultra High Sensitivity Aerosol Spectrometer - Airborne (UHSAS-A, DMT), Passive Cavity Aerosol Spectrometer Probe (PCASP-200, DMT), and Cloud Aerosol Spectrometer (CAS, DMT). Aerosol chemical composition was characterized using a high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS, Aerodyne Inc.) and single particle mass spectrometer, mini-SPLAT. Based on the aerosol size distribution, CCN number concentration (characterized by a DMT dual column CCN counter with a range from 0.1% to 0.4%), and chemical composition, a CCN closure was obtained. The sensitivity of CCN closure to organic hygroscopicity was investigated. The differences in aerosol/CCN properties between two columns, and between two phases, will be discussed.

  15. Aerosol Classification from High Spectral Resolution Lidar Measurements

    NASA Astrophysics Data System (ADS)

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

    2015-12-01

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

  16. Global Aerosol Radiative Forcing Using Satellite and Surface Measurements

    NASA Astrophysics Data System (ADS)

    Patadia, F.; Christopher, S. A.

    2008-05-01

    Over the industrial period, aerosols have increased due to human activities and their effects on climate are the largest source of uncertainty in the current IPCC estimates of global climate forcing due to human activities. Inhomogeneous distribution of aerosols in space and time poses a challenge in characterizing their properties and requires global measurements to assess their effects and reduce the associated uncertainties. In this paper we use global measurements from both satellite and ground based observations for one year time period to estimate the shortwave aerosol radiative forcing (SWARF) at the top-of-atmosphere (TOA) and discuss the associated uncertainties. For this, aerosol properties (optical depth) derived from AErosol RObotic NETwork (AERONET), a federation of ground-based remote sensing instruments, are used in this paper in conjunction with measurements of the TOA shortwave flux from CERES instrument (onboard Terra satellite). High spectral and spatial resolution observations from Imager (MODIS) is used to identify clear sky conditions within CERES foot print and GOCART results will also be used for separating aerosol types. Global aerosol forcing and corresponding radiative forcing efficiencies will be presented as a function of major aerosol types [including anthropogenic (sulfate, soot, black carbon) and natural (dust) aerosols], region and season. This study should serve as a useful constraint for both numerical modeling simulations and satellite based estimates of SWARF.

  17. Combined aerosol in-situ measurements during the SALTRACE field experiment for the investigation of Saharan mineral dust microphysical and CCN properties and their spatial-temporal evolution during trans-Atlantic long-range transport

    NASA Astrophysics Data System (ADS)

    Walser, Adrian; Dollner, Maximilian; Sauer, Daniel; Weinzierl, Bernadett

    2015-04-01

    The Saharan Aerosol Long-range Transport and Aerosol-Cloud-Interaction Experiment (SALTRACE) was a field experiment conducted in June/July 2013, which aimed to investigate the transport and modification of Saharan mineral dust from the Sahara across the Atlantic Ocean to the Caribbean. In addition to ground-based measurements and satellite remote sensing, the DLR Falcon research aircraft was equipped with a number of aerosol in-situ instruments to gain direct information on the properties of airborne aerosol such as size distributions, microphysical, optical and cloud-condensation nuclei (CCN) properties. For the first time, several outbreaks of Saharan dust were probed with the same airborne instrumentation on both sides of the Atlantic. During transport, various processes may take place that modify the aerosol composition. Dry and wet deposition lead to a size-dependent aerosol removal. In case of wet deposition, the removal additionally depends on the particle's ability to act as CCN. Processes in the aqueous phase in subsequently re-evaporating cloud droplets can further alter microphysical and CCN properties of re-released particles. All resulting changes in the size distribution and particle properties impact the radiative feedback and CCN activity of the aged aerosol. This study aims to use combined airborne in-situ measurements to retrieve and compare vertically resolved aerosol size distributions, microphysical and CCN properties for both, short-range transported Saharan dust in the Cape Verde region and long-range transported dust in the Caribbean. We use this data to investigate the influence of long-range transport and associated processes on those properties. We will present vertical profiles of size-resolved aerosol concentrations and volatile fractions as well as CCN activated fractions and draw conclusions for aerosol mixing state, CCN activation diameters and particle hygroscopicities. We will discuss differences in vertical profiles and

  18. Study of aerosol microphysical properties profiles retrieved from ground-based remote sensing and aircraft in-situ measurements during a Saharan dust event

    NASA Astrophysics Data System (ADS)

    Granados-Muñoz, M. J.; Bravo-Aranda, J. A.; Baumgardner, D.; Guerrero-Rascado, J. L.; Pérez-Ramírez, D.; Navas-Guzmán, F.; Veselovskii, I.; Lyamani, H.; Valenzuela, A.; Olmo, F. J.; Titos, G.; Andrey, J.; Chaikovsky, A.; Dubovik, O.; Gil-Ojeda, M.; Alados-Arboledas, L.

    2015-09-01

    In this work we present an analysis of mineral dust optical and microphysical properties obtained from different retrieval techniques applied to active and passive remote sensing measurements, including a comparison with simultaneous in-situ aircraft measurements. Data were collected in a field campaign performed during a mineral dust outbreak a Granada, Spain, experimental site (37.16° N, 3.61° W, 680 m a.s.l.) on the 27 June 2011. Column-integrated properties are provided by sun- and star-photometry which allows a continuous evaluation of the mineral dust optical properties during both day and night-time. Both the Linear Estimation and AERONET (Aerosol Robotic Network) inversion algorithms are applied for the retrieval of the column-integrated microphysical particle properties. In addition, vertically-resolved microphysical properties are obtained from a multi-wavelength Raman lidar system included in EARLINET (European Aerosol Research Lidar Network), by using both LIRIC (Lidar Radiometer Inversion Code) algorithm during daytime and an algorithm applied to the Raman measurements based on the regularization technique during night-time. LIRIC retrievals reveal several dust layers between 3 and 5 km a.s.l. with volume concentrations of the coarse spheroid mode up to 60 μm3 cm-3. The combined use of the regularization and LIRIC methods reveals the night-to-day evolution of the vertical structure of the mineral dust microphysical properties and offers complementary information to that from column-integrated variables retrieved from passive remote sensing. Additionally, lidar depolarization profiles and LIRIC retrieved volume concentration are compared with aircraft in-situ measurements. This study presents for the first time a comparison of both volume concentration and dust particle polarization ratios measured with in-situ and remote sensing techniques. Results for the depolarization measurements in the dust layer indicate reasonable agreement within the

  19. Chemical, physical and radiative properties of atmospheric aerosols measured at Mt. Lulin Atmospheric Background Station (LABS) in East Asia during biomass burning seasons (Invited)

    NASA Astrophysics Data System (ADS)

    Lin, N.; Lee, C.; Wang, S.; Chuang, M.; Chia, E.; Andrews, E.; Ogren, J. A.; Lin, J.; Hung, H.; Hsiao, T.; Liang, S.

    2013-12-01

    This paper presents the chemical, physical and radiative properties of atmospheric aerosols measured at the Lulin Atmospheric Background Station (LABS) which is located at Mt. Lulin (2,862 m MSL; 23o 28'07"N, 120o52'25"E) in central Taiwan, East Asia, and has been operated since 13 April, 2006. LABS is unique because its location and altitude enhances the global network of GAW (Global Atmosphere Watch) in the Southeast Asian region, where no high-elevation baseline station is available. Our site is located between the GAW Waliguan station (3,810 m) on the Tibetan plateau and the Mauna Loa Observatory (3,397m) in Hawaii. We will particularly focus on the results obtained during the spring season, when biomass burning activities prevail in northern Southeast Asia. Chemical characterization of fine and coarse aerosol particles, including water-soluble ions, organic and elemental carbon, and trace elements, will be presented. Aerosol optical properties, including scattering, absorption, extinction, single scattering albedo, Ångström exponent, and aerosol optical depth, as well as the derived radiative forcing efficiency, will be discussed. Results of cloud condensation nuclei measurements, made intermittently, will also be presented. Trajectory studies indicate that this site experiences a variety of air masses originating from contaminated and clean source regions, giving a distinctive contrast of atmospheric changes. To summarize the results, the maximum values (and monthly means) of these chemical, physical and radiative parameters generally occurred during spring time, especially in March, corresponding to prevailing biomass burning activities in SE Asia. Besides, LABS is also one of the supersites during the 2010-2013 spring campaigns of the Seven South East Asian Studies (7-SEAS) for studying the impact of biomass burning on cloud, atmospheric radiation, hydrological cycle, and regional climate over Southeast Asian region. Results of source (northern Thailand

  20. Retrieval of Spectral Aerosol Optical Properties and Their Relationship to Aerosol Chemistry During ARCTAS

    NASA Astrophysics Data System (ADS)

    Corr, C. A.; Hall, S. R.; Ullmann, K.; Shetter, R.; Anderson, B. E.; Beyersdorf, A. J.; Thornhill, K. L.; Cubison, M.; Jimenez, J. L.; Dibb, J. E.

    2010-12-01

    Aerosols are known to both absorb and scatter radiation at UV wavelengths with the degree of absorption/scattering largely dependent on aerosol chemistry. The interactions of aerosols with the UV radiation field were examined during the Arctic Research of the Composition of the Troposphere from Aircraft and Satellites (ARCTAS). Analysis focused on two case studies; one flight from the first phase of ARCTAS over Alaska and the Arctic ocean (Flight 10, April 2008) and the other from the second phase over northern Canada (Flight 17, June 2008). These flights were chosen based on availability of aircraft profiles through pollution layers and biomass burning smoke plumes with high loadings of organic aerosol during flight. Aerosol single scattering albedo (ω) was retrieved at near-UV (350-400nm) wavelengths at 1nm resolution from spectral actinic flux data collected aboard the NASA DC-8 aircraft during ARCTAS using two CCD Actinic Flux Spectroradiometers. Retrievals were performed using the Tropospheric Ultraviolet Model version 4.6 (TUV 4.6). Inputs of trace gas (e.g., NO2, SO2) concentrations, aerosol optical depth, location, time, pressure, etc. required by TUV were determined from ancillary aircraft measurements made from the DC-8. Values of ω were subsequently used to determine absorption optical depth (τabs) for each of the examined flights. Retrieval and calculation results were compared to aerosol optical properties in the visible (calculated from measurements of absorption and scattering aboard the DC-8) and the spectral dependencies characterized. Spectral ω and τabs were compared with aerosol chemistry data collected by an Aerosol Mass Spectrometer (AMS) to provide insight into the role of aerosol composition on absorption in the UV wavelength range. In particular, spectral dependencies were compared to the oxidation state of the organic aerosol (determined from AMS data) to examine the impact of aerosol processing/aging on spectral ω and τabs.

  1. 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.

  2. The New MODIS-Terra, and the Proposed COBRA Mission: First Global Aerosol Distribution and Properties Over Land and Ocean, and Plans to Measure Global Black Carbon Absorption Over the Ocean Glint

    NASA Technical Reports Server (NTRS)

    Kaufman, Yoram J.; Tanre, Didier; Remer, Lorraine; Martins, Vanderlei; Schoeberl, Mark; Lau, William K. M. (Technical Monitor)

    2001-01-01

    The MODIS instrument was launched on the NASA Terra satellite in Dec. 1999. Since last Oct, the sensor and the aerosol algorithm reached maturity and provide global daily retrievals of aerosol optical thickness and properties. MODIS has 36 spectral channels in the visible to IR with resolution down to 250 m. This allows accurate cloud screening and multi-spectral aerosol retrievals. We derive the aerosol optical thickness over the ocean and most of the land areas, distinguishing between fine (mainly man-made aerosol) and coarse (mainly natural) aerosol particles. New methods to derive the aerosol absorption of sunlight are also being developed. These measurements are use to track different aerosol sources, transport and the radiative forcing at the top and bottom of the atmosphere. However MODIS or any present satellite sensor cannot measure absorption by Black Carbon over the oceans, a critical component in studying climate change and human health. For this purpose we propose the COBRA mission that observes the ocean at glint and off glint simultaneously measuring the spectral polarized light and deriving precisely the aerosol absorption.

  3. Estimating aerosol light-scattering enhancement from dry aerosol optical properties at different sites

    NASA Astrophysics Data System (ADS)

    Titos, Gloria; Jefferson, Anne; Sheridan, Patrick; Andrews, Elisabeth; Lyamani, Hassan; Ogren, John; Alados-Arboledas, Lucas

    2014-05-01

    Microphysical and optical properties of aerosol particles are strongly dependent on the relative humidity (RH). Knowledge of the effect of RH on aerosol optical properties is of great importance for climate forcing calculations and for comparison of in-situ measurements with satellite and remote sensing retrievals. The scattering enhancement factor, f(RH), is defined as the ratio of the scattering coefficient at a high and reference RH. Predictive capability of f(RH) for use in climate models would be enhanced if other aerosol parameters could be used as proxies to estimate hygroscopic growth. Toward this goal, we explore the relationship between aerosol light-scattering enhancement and dry aerosol optical properties such as the single scattering albedo (SSA) and the scattering Ångström exponent (SAE) at multiple sites around the world. The measurements used in this study were conducted by the US Department of Energy at sites where different aerosol types predominate (pristine marine, polluted marine, dust dominated, agricultural and forest environments, among others). In all cases, the scattering enhancement decreases as the SSA decreases, that is, as the contribution of absorbing particles increases. On the other hand, for marine influenced environments the scattering enhancement clearly increases as the contribution of coarse particles increases (SAE decreases), evidence of the influence of hygroscopic coarse sea salt particles. For other aerosol types the relationship between f(RH) and SAE is not so straightforward. Combining all datasets, f(RH) was found to exponentially increase with SSA with a high correlation coefficient.

  4. Aerosol extinction measurements with CO2-lidar

    NASA Technical Reports Server (NTRS)

    Hagard, Arne; Persson, Rolf

    1992-01-01

    With the aim to develop a model for infrared extinction due to aerosols in slant paths in the lower atmosphere we perform measurements with a CO2-lidar. Earlier measurements with a transmissometer along horizontal paths have been used to develop relations between aerosol extinction and meteorological parameters. With the lidar measurements we hope to develop corresponding relations for altitude profiles of the aerosol extinction in the infrared. An important application is prediction of detection range for infrared imaging systems.

  5. Influence of semi-volatile aerosol on physical and optical properties of aerosol in Kathmandu valley

    NASA Astrophysics Data System (ADS)

    Shrestha, Sujan; Praveen, Ps; Adhikary, Bhupesh; Shrestha, Kundan; Panday, Arnico

    2016-04-01

    A field study was conducted in the urban atmosphere of Kathmandu valley to study the influence of the semi-volatile aerosol fraction on physical and optical properties of aerosols. The study was carried out during the 2015 pre-monsoon period. Experimental setup consisted of air from an ambient air inlet being split to two sets of identical sampling instruments. The first instrument received the ambient sample directly, while the second instrument received the air sample through a thermodenuder (TDD). Four sets of experiments were conducted to understand aerosol number, size distribution, scattering and absorption properties using Condensation Particle Counter (CPC), Scanning Mobility Particle Sizer (SMPS), Aethalometer (AE33) and Nephelometer. The influence of semi-volatile aerosols was calculated from the fraction of particles evaporated in the TDD at set temparetures: room temperature, 50°C, 100°C, 150°C, 200°C, 250°C and 300°C. Results show that, with increasing temperature, the evaporated fraction of semi-volatile aerosol also increased. At room temperature the fraction of semi-volatile aerosols was 12% while at 300°C it was as high as to 49%. Aerosol size distribution analysis shows that with an increase in TDD temperature from 50°C to 300°C, peak mobility diameter of particles shifted from around 60nm to 40nm. However we found little change in effective diameter of aerosol size distribution with increase in set TDD temperature. The change in size of aerosols due to loss of semi-volatile component has a stronger influence (~70%) in higher size bins when compared to at lower size bins (~20%). Studies using the AE33 showed that absorption by black carbon (BC) is amplified due to influence of semi-volatile aerosols by upto 37% at 880nm wavelength. Similarly nephelometer measurements showed that upto 71% of total scattering was found to be contributed by semi-volatile aerosol fraction. The scattering Angstrom Exponent (SAE) of semi-volatile aerosol

  6. 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.

  7. Aerosol physical properties and their impact on climate change processes

    NASA Astrophysics Data System (ADS)

    Strzalkowska, Agata; Zielinski, Tymon; Petelski, Tomasz; Makuch, Przemyslaw; Pakszys, Paulina; Markuszewski, Piotr; Piskozub, Jacek; Drozdowska, Violetta; Gutowska, Dorota; Rozwadowska, Anna

    2013-04-01

    Characterizing aerosols involves the specification of not only their spatial and temporal distributions but their multi-component composition, particle size distribution and physical properties as well. Due to their light attenuation and scattering properties, aerosols influence radiance measured by satellite for ocean color remote sensing. Studies of marine aerosol production and transport are important for many earth sciences such as cloud physics, atmospheric optics, environmental pollution studies, and interaction between ocean and atmosphere. It was one of the reasons for the growth in the number of research programs dealing with marine aerosols. Sea salt aerosols are among the most abundant components of the atmospheric aerosol, and thus it exerts a strong influence on radiation, cloud formation, meteorology and chemistry of the marine atmosphere. An accurate understanding and description of these mechanisms is crucial to modeling climate and climate change. This work provides information on combined aerosol studies made with lidars and sun photometers onboard the ship and in different coastal areas. We concentrate on aerosol optical thickness and its variations with aerosol advections into the study area. We pay special attention to the problem of proper data collection and analyses techniques. We showed that in order to detect the dynamics of potential aerosol composition changes it is necessary to use data from different stations where measurements are made using the same techniques. The combination of such information with air mass back-trajectories and data collected at stations located on the route of air masses provides comprehensive picture of aerosol variations in the study area both vertically and horizontally. Acknowledgements: The support for this study was provided by the project Satellite Monitoring of the Baltic Sea Environment - SatBałtyk founded by European Union through European Regional Development Fund contract No. POIG 01

  8. Global Aerosol Radiative Forcing using Satellite and Surface Measurements

    NASA Astrophysics Data System (ADS)

    Patadia, F.; Christopher, S. A.

    2007-12-01

    Over the industrial period, aerosols have increased due to human activities and their effects on climate are the largest source of uncertainty in the current IPCC estimates of global climate forcing due to human activities. Inhomogeneous distribution of aerosols in space and time poses a challenge in their characterization and requires global measurements to assess their effects and reduce the associated uncertainties. In this paper we use global measurements from both satellite and ground based observations for one year time period to estimate the shortwave aerosol radiative forcing (SWARF) at the top-of-atmosphere (TOA) and discuss the associated uncertainties. For this, aerosol properties (optical depth) derived from AErosol RObotic NETwork (AERONET), a federation of ground-based remote sensing instruments, are used in this paper in conjunction with measurements of the TOA shortwave flux from CERES instrument (onboard Terra satellite). High spectral and spatial resolution observations from Imager (MODIS) will be used to identify clear sky conditions within CERES foot print and GOCART results will also be used for separating aerosol types. Global aerosol forcing and corresponding radiative forcing efficiencies will be presented as a function of major aerosol types [including anthropogenic (sulfate, soot, black carbon) and natural (dust) aerosols], region and season. This study should serve as a useful constraint for both numerical modeling simulations and satellite based estimates of SWARF.

  9. Importance of Raman Lidar Aerosol Extinction Measurements for Aerosol-Cloud Interaction Studies

    NASA Astrophysics Data System (ADS)

    Han, Zaw; Wu, Yonghua; Moshary, Fred; Gross, Barry; Gilerson, Alex

    2016-06-01

    Using a UV Raman Lidar for aerosol extinction, and combining Microwave Radiometer derived Liquid Water Path (LWP) with Multifilter Rotating Shadowband Radiometer derived Cloud Optical depth, to get cloud effective radius (Reff), we observe under certain specialized conditions, clear signatures of the Twomey Aerosol Indirect effect on cloud droplet properties which are consistent with the theoretical bounds. We also show that the measurement is very sensitive to how far the aerosol layer is from the cloud base and demonstrate that surface PM25 is far less useful. Measurements from both the DOE ARM site and new results at CCNY are presented.

  10. 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.

  11. Global Analysis of Aerosol Properties Above Clouds

    NASA Technical Reports Server (NTRS)

    Waquet, F.; Peers, F.; Ducos, F.; Goloub, P.; Platnick, S. E.; Riedi, J.; Tanre, D.; Thieuleux, F.

    2013-01-01

    The seasonal and spatial varability of Aerosol Above Cloud (AAC) properties are derived from passive satellite data for the year 2008. A significant amount of aerosols are transported above liquid water clouds on the global scale. For particles in the fine mode (i.e., radius smaller than 0.3 m), including both clear sky and AAC retrievals increases the global mean aerosol optical thickness by 25(+/- 6%). The two main regions with man-made AAC are the tropical Southeast Atlantic, for biomass burning aerosols, and the North Pacific, mainly for pollutants. Man-made AAC are also detected over the Arctic during the spring. Mineral dust particles are detected above clouds within the so-called dust belt region (5-40 N). AAC may cause a warming effect and bias the retrieval of the cloud properties. This study will then help to better quantify the impacts of aerosols on clouds and climate.

  12. Aerosol optical absorption measurements with photoacoustic spectroscopy

    NASA Astrophysics Data System (ADS)

    Liu, Kun; Wang, Lei; Liu, Qiang; Wang, Guishi; Tan, Tu; Zhang, Weijun; Chen, Weidong; Gao, Xiaoming

    2015-04-01

    Many parameters related to radiative forcing in climate research are known only with large uncertainties. And one of the largest uncertainties in global radiative forcing is the contribution from aerosols. Aerosols can scatter or absorb the electromagnetic radiation, thus may have negative or positive effects on the radiative forcing of the atmosphere, respectively [1]. And the magnitude of the effect is directly related to the quantity of light absorbed by aerosols [2,3]. Thus, sensitivity and precision measurement of aerosol optical absorption is crucial for climate research. Photoacoustic spectroscopy (PAS) is commonly recognized as one of the best candidates to measure the light absorption of aerosols [4]. A PAS based sensor for aerosol optical absorption measurement was developed. A 532 nm semiconductor laser with an effective power of 160 mW was used as a light source of the PAS sensor. The PAS sensor was calibrated by using known concentration NO2. The minimum detectable optical absorption coefficient (OAC) of aerosol was determined to be 1 Mm-1. 24 hours continues measurement of OAC of aerosol in the ambient air was carried out. And a novel three wavelength PAS aerosol OAC sensor is in development for analysis of aerosol wavelength-dependent absorption Angstrom coefficient. Reference [1] U. Lohmann and J. Feichter, Global indirect aerosol effects: a review, Atmos. Chem. Phys. 5, 715-737 (2005) [2] M. Z. Jacobson, Strong radiative heating due to the mixing state of black carbon in atmospheric aerosols, Nature 409, 695-697 (2001) [3] V. Ramanathan and G. Carmichae, Global and regional climate changes due to black carbon, nature geoscience 1, 221-227 (2008) [4] W.P Arnott, H. Moosmuller, C. F. Rogers, T. Jin, and R. Bruch, Photoacoustic spectrometer for measuring light absorption by aerosol: instrument description. Atmos. Environ. 33, 2845-2852 (1999).

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

    SciTech Connect

    Dr. Timothy Onasch

    2009-09-09

    This SBIR Phase I project addressed the critical need for improved characterization of carbonaceous aerosol species in the atmosphere. The proposed work focused on the development of a thermodenuder (TD) system capable of systematically measuring volatility profiles of primary and secondary organic aerosol species and providing insight into the effects of absorbing and nonabsorbing organic coatings on particle absorption properties. This work provided the fundamental framework for the generation of essential information needed for improved predictions of ambient aerosol loadings and radiative properties by atmospheric chemistry models. As part of this work, Aerodyne Research, Inc. (ARI) continued to develop and test, with the final objective of commercialization, an improved thermodenuder system that can be used in series with any aerosol instrument or suite of instruments (e.g., aerosol mass spectrometers-AMS, scanning mobility particle sizers-SMPS, photoacoustic absorption spectrometers-PAS, etc.) to obtain aerosol chemical, physical, and optical properties as a function of particle volatility. In particular, we provided the proof of concept for the direct coupling of our improved TD design with a full microphysical model to obtain volatility profiles for different organic aerosol components and to allow for meaningful comparisons between different TD-derived aerosol measurements. In a TD, particles are passed through a heated zone and a denuding (activated charcoal) zone to remove semi-volatile material. Changes in particle size, number concentration, optical absorption, and chemical composition are subsequently detected with aerosol instrumentation. The aerosol volatility profiles provided by the TD will strengthen organic aerosol emission inventories, provide further insight into secondary aerosol formation mechanisms, and provide an important measure of particle absorption (including brown carbon contributions and identification, and absorption enhancements

  14. Aerosol physical properties from satellite horizon inversion

    NASA Technical Reports Server (NTRS)

    Gray, C. R.; Malchow, H. L.; Merritt, D. C.; Var, R. E.; Whitney, C. K.

    1973-01-01

    The feasibility is investigated of determining the physical properties of aerosols globally in the altitude region of 10 to 100 km from a satellite horizon scanning experiment. The investigation utilizes a horizon inversion technique previously developed and extended. Aerosol physical properties such as number density, size distribution, and the real and imaginary components of the index of refraction are demonstrated to be invertible in the aerosol size ranges (0.01-0.1 microns), (0.1-1.0 microns), (1.0-10 microns). Extensions of previously developed radiative transfer models and recursive inversion algorithms are displayed.

  15. Hygroscopic properties and mixing state of aerosol measured at the high-altitude site Puy de Dôme (1465 m a.s.l.), France

    NASA Astrophysics Data System (ADS)

    Holmgren, H.; Sellegri, K.; Hervo, M.; Rose, C.; Freney, E.; Villani, P.; Laj, P.

    2014-09-01

    A Hygroscopicity Tandem Differential Mobility Analyser (HTDMA) was used to evaluate the hygroscopic properties of aerosol particles measured at the Puy de Dôme research station in central France, periodically from September 2008 to January 2010, and almost continuously from October 2010 to December 2012. This high-altitude site is ideally situated to allow for both the upper part of the planetary boundary layer and the lower free troposphere to be sampled. The aim of the study is to investigate both the influence of year-to-year, seasonal and diurnal cycles, as well as the influence of air mass type on particle hygroscopicity and mixing state. Results show that particle hygroscopicity increases with particle size and depends both on air mass type and on season. Average growth factor values, GFs, are lowest in winter (1.21 ± 0.13, 1.23 ± 0.18 and 1.38 ± 0.25 for 25, 50 and 165 nm particles, respectively) and highest in autumn (1.27 ± 0.11, 1.32 ± 0.12 and 1.49 ± 0.15 for 25, 50 and 165 nm particles, respectively). Particles are generally more hygroscopic at night than during the day. The seasonal and diurnal variations are likely to be strongly influenced by boundary layer dynamics. Furthermore, particles originating from oceanic and continental regions tend to be more hygroscopic than those measured in African and local air masses. The high hygroscopicity of oceanic aerosol can be explained by large proportions of inorganic aerosol and sea salts. Aerosols measured at the Puy de Dôme display a high degree of external mixing, and hygroscopic growth spectra can be divided into three different hygroscopic modes: a less-hygroscopic mode (GF < 1.3), a hygroscopic mode (GF 1.3-1.7) and a more-hygroscopic mode (GF > 1.7). The majority of particles measured can be classified as being in either the less-hygroscopic mode or the hygroscopic mode, and only few of them have more-hygroscopic properties. The degree of external mixing, evaluated as the fraction of time when

  16. Retrieval of Aerosol Microphysical Properties from MFRSR Observations

    SciTech Connect

    Kassianov, Evgueni I; Barnard, James C; Ackerman, Thomas P

    2006-05-01

    Aerosols can have significant impact on the radiative and heat balance of the Earth-atmosphere system by absorbing and scattering solar radiation (direct aerosol effect) and altering cloud optical properties and suppressing precipitation (indirect aerosol effect). However, both the sign and magnitude of the aerosol impact has proven difficult to determine due to incomplete knowledge of aerosol properties and their strong temporal and spatial variations. Reduction of these uncertainties requires an accurate global inventory of aerosol microphysical properties, such as size distribution and the refractive index. Multi-filter Rotating Shadowband Radiometers (MFRSRs) are widely deployed over the world (e.g., the surface radiation budget network). These radiometers provide measurements of the direct and the diffuse solar irradiances at six wavelengths (0.415, 0.5, 0.615, 0.673, 0.870 and 0.94 ). Currently, the direct irradiance observations are used to derive routinely spectral values of the aerosol optical depth only. We propose a simple retrieval technique that significantly extends the capability of the MFRSR to study atmospheric aerosols. In our retrieval, we assume the shape of aerosol size distribution (e.g., combination of three lognormal distributions) and the value of the real refractive index. The technique consists of three steps that compose an iterative scheme. The first step obtains the aerosol size distribution from the spectral measurements of the direct irradiance (for a given complex refractive index). To reduce the effect of ozone and water vapor contamination, we use wavelengths where ozone and water vapor weakly affect the direct irradiance (0.415 mu and 0.870 mu). The second step determines the effective value of the imaginary refractive index from the diffuse irradiance (for the aerosol size distribution determined during the first step). To reduce the effect of the surface albedo on the retrievals, we select a wavelength where the surface albedo

  17. 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.

  18. Hygroscopic properties and mixing state of aerosol measured at the high altitude site Puy de Dôme (1465 m a.s.l.), France

    NASA Astrophysics Data System (ADS)

    Holmgren, H.; Sellegri, K.; Hervo, M.; Rose, C.; Freney, E.; Villani, P.; Laj, P.

    2014-03-01

    A Hygroscopicity Tandem Differential Mobility Analyzer (HTDMA) was used to evaluate the hygroscopic properties of aerosol particles measured at the Puy de Dôme research station in central France from September 2008 to December 2012. This high-altitude site is ideally situated to allow for both the upper part of the planetary boundary layer and the lower free troposphere to be sampled. The aim of the study is to investigate both the influence of year-to-year, seasonal, and diurnal cycles, as well as the influence of air mass type on particle hygroscopicity and mixing state. Results show that particle hygroscopicity increases with particle size and depends both on air mass type and on season. Average growth factor values are lowest in winter (1.21 ± 0.13, 1.23 ± 0.18 and 1.38 ± 0.25 for 25, 50 and 165 nm particles, respectively) and highest in autumn (1.27 ± 0.11, 1.32 ± 0.12 and 1.49 ± 0.15 for 25, 50 and 165 nm particles, respectively). Particles are generally more hygroscopic at night than during the day. The seasonal and diurnal variations are likely to be strongly influenced by boundary layer dynamics. Furthermore, particles originating from oceanic and continental regions tend to be more hygroscopic than those measured in African and local air masses. The high hygroscopicity of marine aerosol may be explained by large proportions of inorganic aerosol and sea salts, and it is speculated that continental particles are more hygroscopic than local and African ones due to ageing of fresh combustion aerosol. Aerosol measured at the Puy de Dôme display a high degree of external mixing, and hygroscopic growth spectra can be divided into three different hygroscopic modes: a less hygroscopic mode (GF < 1.3), a hygroscopic mode (GF 1.3-1.7) and a more hygroscopic mode (GF > 1.7). The majority of particles measured can be classified as being in either the less hygroscopic mode or the hygroscopic mode, and only few of them have more hygroscopic properties. The

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

    SciTech Connect

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

    2007-09-30

    The optical properties of aerosol particles are the controlling factors in determining direct aerosol radiative forcing. These optical properties depend on the chemical composition and size distribution of the aerosol particles, which can change due to various processes during the particles’ lifetime in the atmosphere. Over the course of this project we have studied how cloud processing of atmospheric aerosol changes the aerosol optical properties. A counterflow virtual impactor was used to separate cloud drops from interstitial aerosol and parallel aerosol systems were used to measure the optical properties of the interstitial and cloud-scavenged aerosol. Specifically, aerosol light scattering, back-scattering and absorption were measured and used to derive radiatively significant parameters such as aerosol single scattering albedo and backscatter fraction for cloud-scavenged and interstitial aerosol. This data allows us to demonstrate that the radiative properties of cloud-processed aerosol can be quite different than pre-cloud aerosol. These differences can be used to improve the parameterization of aerosol forcing in climate models.

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

    SciTech Connect

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

    2009-03-05

    The optical properties of aerosol particles are the controlling factors in determining direct aerosol radiative forcing. These optical properties depend on the chemical composition and size distribution of the aerosol particles, which can change due to various processes during the particles’ lifetime in the atmosphere. Over the course of this project we have studied how cloud processing of atmospheric aerosol changes the aerosol optical properties. A counterflow virtual impactor was used to separate cloud drops from interstitial aerosol and parallel aerosol systems were used to measure the optical properties of the interstitial and cloud-scavenged aerosol. Specifically, aerosol light scattering, back-scattering and absorption were measured and used to derive radiatively significant parameters such as aerosol single scattering albedo and backscatter fraction for cloud-scavenged and interstitial aerosol. This data allows us to demonstrate that the radiative properties of cloud-processed aerosol can be quite different than pre-cloud aerosol. These differences can be used to improve the parameterization of aerosol forcing in climate models.

  1. In situ measurements of aerosol optical properties and number size distributions in a coastal region of Norway during the summer of 2008

    NASA Astrophysics Data System (ADS)

    Mogo, S.; Cachorro, V. E.; Lopez, J. F.; Montilla, E.; Torres, B.; Rodríguez, E.; Bennouna, Y.; de Frutos, A. M.

    2012-07-01

    In situ measurements of aerosol optical properties and particle size distributions were made in the summer of 2008 at the ALOMAR station facility (69°16' N, 16°00' E), located in a rural site in the north of the island of Andøya (Vesterålen archipelago), approximately 300 km north of the Arctic Circle. The extended three-month campaign was part of the POLARCAT Project (Polar Study using Aircraft, Remote Sensing, Surface Measurements and Models, of Climate, Chemistry, Aerosols, and Transport) of the International Polar Year (IPY-2007-2008). Our goal was to characterize the aerosols of this sub-Arctic area, which are frequently transported to the Arctic region. Data from 13 June to 26 August 2008 were available and the statistical data for all instruments were calculated based on the hourly averages. The overall data coverage was approximately 72%. The hourly mean values of the light-scattering coefficient, σs, and the light-absorption coefficient, σa, at 550 nm were 5.41 Mm-1 (StD = 3.55 Mm-1) and 0.40 Mm-1 (StD = 0.27 Mm-1), respectively. The scattering/absorption Ångström exponents, αs,a, were used in a detailed analysis of the variations of the spectral shape of σs,a. While αs indicates the presence of two particle sizes corresponding to two types of aerosols, αa indicates only one type of absorbing aerosol particle. αa values greater than 1 were not observed. The single-scattering albedo, ω0, ranged from 0.62 to 0.99 (mean = 0.91, StD = 0.05), and the relationships between this parameter and the absorption/scattering coefficients and the Ångström exponents are presented. Any absorption value may lead to the lowest values of ω0, whereas only the lowest scattering values were observed in the lowest range of ω0. For a given absorption value, lower ω0 were observed for smaller αs. The submicrometer, micrometer and total concentrations of the particles presented hourly mean values of 1277 cm-3 (StD = 1563 cm-3), 1 cm-3 (StD = 1 cm-3) and 2463 cm-3

  2. Aerosol scattering optical properties by nephelometer measurements at the El Arenosillo site (SW coastal area of Spain)

    NASA Astrophysics Data System (ADS)

    López, Juan F.; Cachorro, Victoria E.; de Frutos, Ángel

    2013-05-01

    Aerosol light scattering coefficients, the hemispheric σsp and the back-scattering coefficient σbsc, have been measured using a 3-wavelengths integrating nephelometer over two years (January 2006 to May 2008) at the monitoring station ESAT-El Arenosillo. This station is located in the coastal area of the province of Huelva, in the southwest of the Iberian, Peninsula. The Ångström exponent α, has been also derived from the spectral dependence of σsp. All these parameters have been carefully analyzed to investigate their general characteristics and features, and diurnal variability. A general statistic gives mean values and std of σsp = 48.5 ±38.1 Mm-1 with a large range of variation showing moderate values of this rural and coastal site with marine prevalence but with significant influence of local sources of pollution. The daily cycle of σsp and α presents different behaviour depending on the season and is modulated by sea-land breeze regime.

  3. Surface Measurements of dust/local aerosol properties over Northern China during 2008 China-US joined dust field campaign

    NASA Astrophysics Data System (ADS)

    Wang, X.; Huang, J.

    2009-12-01

    The objective of this study is to understand the detailed characteristics and underlying mechanisms of aerosol physical and optical parameters over China Loess Plateau and its potential impacts on the regional/global climate. In order to characterize the emission, transport, and removal of atmospheric pollutants emitted from East Asia, the 2008 China-US joined field campaign are conducted from late April to May 2008 focused specifically on the Asian direct measurements of dust and pollution transport, following the plume from the Northern China which from the Taklamakan desert and Gobi desert to the Eastern Pacific and into North America. Such measurements are crucial to understanding how the dust and the pollution plume (including black carbon) are modified as their age. Three sites involved this campaign, including one permanent site (Semi-Arid Climate & Environment Observatory of Lanzhou University (SACOL)) (located in Yuzhong, 35.95N/104.1E), one SACOL's Mobile Facility (SMF) (deployed in Jintai, 37.57N/104.23E) and the U.S. Department of Energy Atmospheric Radiation Measurements(ARM) Ancillary Facility (AAF mobile laboratories, SMART-COMMIT) (deployed in Zhangye, 39.08N/100.27E). Results indicate that the dust plumes are transported from the surface to a long distance from their sources have a significant influence on the air quality in the study area. The meteorological analysis indicates that these polluted layers are not from local sources during dust plume and this large-scale transport of dust and pollutants remains a major uncertainty in quantifying the global effect of emissions from Northern China.

  4. Aerosol classification using EARLINET measurements for an intensive observational period

    NASA Astrophysics Data System (ADS)

    Papagiannopoulos, Nikolaos; Mona, Lucia; Pappalardo, Gelsomina

    2016-04-01

    ACTRIS (Aerosols, Clouds and Trace gases Research Infrastructure Network) organized an intensive observation period during summer 2012. This campaign aimed at the provision of advanced observations of physical and chemical aerosol properties, at the delivery of information about the 3D distribution of European atmospheric aerosols, and at the monitoring of Saharan dust intrusions events. EARLINET (European Aerosol Research Lidar Network) participated in the ACTRIS campaign through the addition of measurements according to the EARLINET schedule as well as daily lidar-profiling measurements around sunset by 11 selected lidar stations for the period from 8 June - 17 July. EARLINET observations during this almost two-month period are used to characterize the optical properties and vertical distribution of long-range transported aerosol over the broader area of Mediterranean basin. The lidar measurements of aerosol intensive parameters (lidar ratio, depolarization, Angstrom exponents) are shown to vary with location and aerosol type. A methodology based on EARLINET observations of frequently observed aerosol types is used to classify aerosols into seven separate types. The summertime Mediterranean basin is prone to African dust aerosols. Two major dust events were studied. The first episode occurred from the 18 to 21 of the June and the second one lasted from 28 June to 6 July. The lidar ratio within the dust layer was found to be wavelength independent with mean values of 58±14 sr at 355 nm and 57±11 sr at 532 nm. For the particle linear depolarization ratio, mean values of 0.27±0.04 at 532 nm have been found. Acknowledgements. The financial support for EARLINET in the ACTRIS Research Infrastructure Project by the European Union's Horizon 2020 research and innovation programme under grant agreement no. 654169 and previously under grant agreement no. 262254 in the Seventh Framework Programme (FP7/2007-2013) is gratefully acknowledged.

  5. Atmospheric DMS and Biogenic Sulfur aerosol measurements in the Arctic

    NASA Astrophysics Data System (ADS)

    Ghahremaninezhadgharelar, R.; Norman, A. L.; Wentworth, G.; Burkart, J.; Leaitch, W. R.; Abbatt, J.; Sharma, S.; Desiree, T. S.

    2014-12-01

    Dimethyl Sulfide (DMS) and its oxidation products were measured on the board of the Canadian Coast Guard Ship (CCGS) Amundsen and above melt ponds in the Arctic during July 2014 in the context of the NETCARE study which seeks to understand the effect of DMS and its oxidation products with respect to aerosol nucleation, as well as its effect on cloud and precipitation properties. The objective of this study is to quantify the role of DMS in aerosol growth and activation in the Arctic atmosphere. Atmospheric DMS samples were collected from different altitudes, from 200 to 9500 feet, aboard the POLAR6 aircraft expedition to determine variations in the DMS concentration and a comparison was made to shipboard DMS measurements and its effects on aerosol size fractions. The chemical and isotopic composition of sulfate aerosol size fractions was studied. Sulfur isotope ratios (34S/32S) offer a way to determine the oceanic DMS contribution to aerosol growth. The results are expected to address the contribution of anthropogenic as well as biogenic sources of aerosols to the growth of the different aerosol size fractions. In addition, aerosol sulfate concentrations were measured at the same time within precipitation and fogs to compare with the characteristics of aerosols in each size fraction with the characteristics of the sulfate in each medium. This measurement is expected to explain the contribution of DMS oxidation in aerosol activation in the Arctic summer. Preliminary results from the measurement campaign for DMS and its oxidation products in air, fog and precipitation will be presented.

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

    NASA Astrophysics Data System (ADS)

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

    2007-11-01

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

  7. An aerosol climatology for a rapidly growing arid region (southern Arizona): Major aerosol species and remotely sensed aerosol properties

    PubMed Central

    Sorooshian, Armin; Wonaschütz, Anna; Jarjour, Elias G.; Hashimoto, Bryce I.; Schichtel, Bret A.; Betterton, Eric A.

    2014-01-01

    This study reports a comprehensive characterization of atmospheric aerosol particle properties in relation to meteorological and back trajectory data in the southern Arizona region, which includes two of the fastest growing metropolitan areas in the United States (Phoenix and Tucson). Multiple data sets (MODIS, AERONET, OMI/TOMS, MISR, GOCART, ground-based aerosol measurements) are used to examine monthly trends in aerosol composition, aerosol optical depth (AOD), and aerosol size. Fine soil, sulfate, and organics dominate PM2.5 mass in the region. Dust strongly influences the region between March and July owing to the dry and hot meteorological conditions and back trajectory patterns. Because monsoon precipitation begins typically in July, dust levels decrease, while AOD, sulfate, and organic aerosol reach their maximum levels because of summertime photochemistry and monsoon moisture. Evidence points to biogenic volatile organic compounds being a significant source of secondary organic aerosol in this region. Biomass burning also is shown to be a major contributor to the carbonaceous aerosol budget in the region, leading to enhanced organic and elemental carbon levels aloft at a sky-island site north of Tucson (Mt. Lemmon). Phoenix exhibits different monthly trends for aerosol components in comparison with the other sites owing to the strong influence of fossil carbon and anthropogenic dust. Trend analyses between 1988 and 2009 indicate that the strongest statistically significant trends are reductions in sulfate, elemental carbon, and organic carbon, and increases in fine soil during the spring (March–May) at select sites. These results can be explained by population growth, land-use changes, and improved source controls. PMID:24707452

  8. Climatology and Characteristics of Aerosol Optical Properties in the Arctic

    NASA Astrophysics Data System (ADS)

    Schmeisser, Lauren; Ogren, John; Backman, John; Asmi, Eija; Andrews, Elisabeth; Jefferson, Anne; Bergin, Michael; Tunved, Peter; Sharma, Sangeeta; Starkweather, Sandra

    2016-04-01

    Within the Arctic, climate forcers like atmospheric aerosols are important contributors to the observed warming and environmental changes in the region. Quantifying the forcing by aerosols in the Arctic is especially difficult, given short aerosol lifetimes, annual variability in illumination and surface albedo, stratified atmospheric conditions, complex feedbacks, and long-range aerosol transport. However, in-situ surface measurements of Arctic aerosol optical properties can be used to constrain variability of light scattering and absorption, identify potential particle sources, and help evaluate the resulting forcing. Data from six WMO Global Atmosphere Watch stations are presented: Alert, Canada (ALT); Barrow, Alaska (BRW); Pallas, Finland (PAL); Summit, Greenland (SUM); Tiksi, Russia (TIK); and Zeppelin Mountain, Norway (ZEP). These sites contribute to the International Arctic System for Observing the Atmosphere (IASOA), which facilitates Arctic-wide data collection and analysis. Climatologies of aerosol optical properties from each station show differences in magnitude and variability of observed parameters. For example, most stations (ALT, BRW, SUM, TIK, ZEP) experience maximum scattering in winter/spring, while PAL exhibits maximum scattering in the summer. The observed range in scattering across these sites is large (almost an order of magnitude) - SUM has the lowest annual median scattering at 0.82 Mm-1 while BRW has the highest at 6.9 Mm-1. A closer look at systematic variability between optical properties at each station, as well as site back trajectories, suggest differences in aerosol processes, sources and transport. The development of consistent climatologies and additional analyses like the ones presented here can help provide a better understanding of trans-Arctic aerosol variability, which can be an asset for improving aerosol models in this unique and remote region.

  9. Improving satellite-retrieved aerosol microphysical properties using GOCART data

    NASA Astrophysics Data System (ADS)

    Li, S.; Kahn, R.; Chin, M.; Garay, M. J.; Liu, Y.

    2015-03-01

    The Multi-angle Imaging SpectroRadiometer (MISR) aboard the NASA Earth Observing System's Terra satellite can provide more reliable aerosol optical depth (AOD) and better constraints on particle size (Ångström exponent, or ANG), sphericity, and single-scattering albedo (SSA) than many other satellite instruments. However, many aerosol mixtures pass the algorithm acceptance criteria, yielding a poor constraint, when the particle-type information in the MISR radiances is low, typically at low AOD. We investigate adding value to the MISR aerosol product under these conditions by filtering the list of MISR-retrieved mixtures based on agreement between the mixture ANG and absorbing AOD (AAOD) values, and simulated aerosol properties from the Goddard Chemistry Aerosol Radiation and Transport (GOCART) model. MISR-GOCART ANG difference and AAOD ratio thresholds for applying GOCART constraints were determined based on coincident AOD, ANG, and AAOD measurements from the AErosol RObotic NETwork (AERONET). The results were validated by comparing the adjusted MISR aerosol optical properties over the contiguous USA between 2006 and 2009 with additional AERONET data. The correlation coefficient (r) between the adjusted MISR ANG derived from this study and AERONET improves to 0.45, compared to 0.29 for the MISR Version 22 standard product. The ratio of the adjusted MISR AAOD to AERONET increases to 0.74, compared to 0.5 for the MISR operational retrieval. These improvements occur primarily when AOD < 0.2 for ANG and AOD < 0.5 for AAOD. Spatial and temporal differences among the aerosol optical properties of MISR V22, GOCART, and the adjusted MISR are traced to (1) GOCART underestimation of AOD and ANG in polluted regions; (2) aerosol mixtures lacking in the MISR Version 22 algorithm climatology; (3) low MISR sensitivity to particle type under some conditions; and (4) parameters and thresholds used in our method.

  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. Workplace aerosol mass concentration measurement using optical particle counters.

    PubMed

    Görner, Peter; Simon, Xavier; Bémer, Denis; Lidén, Göran

    2012-02-01

    Direct-reading aerosol measurement usually uses the optical properties of airborne particles to detect and measure particle concentration. In the case of occupational hygiene, mass concentration measurement is often required. Two aerosol monitoring methods are based on the principle of light scattering: optical particle counting (OPC) and photometry. The former analyses the light scattered by a single particle, the latter by a cloud of particles. Both methods need calibration to transform the quantity of scattered light detected into particle concentration. Photometers are simpler to use and can be directly calibrated to measure mass concentration. However, their response varies not only with aerosol concentration but also with particle size distribution, which frequently contributes to biased measurement. Optical particle counters directly measure the particle number concentration and particle size that allows assessment of the particle mass provided the particles are spherical and of known density. An integrating algorithm is used to calculate the mass concentration of any conventional health-related aerosol fraction. The concentrations calculated thus have been compared with simultaneous measurements by conventional gravimetric sampling to check the possibility of field OPC calibration with real workplace aerosols with a view to further monitoring particle mass concentration. Aerosol concentrations were measured in the food industry using the OPC GRIMM® 1.108 and the CIP 10-Inhalable and CIP 10-Respirable (ARELCO®) aerosol samplers while meat sausages were being brushed and coated with calcium carbonate. Previously, the original OPC inlet had been adapted to sample inhalable aerosol. A mixed aerosol of calcium carbonate and fungi spores was present in the workplace. The OPC particle-size distribution and an estimated average particle density of both aerosol components were used to calculate the mass concentration. The inhalable and respirable aerosol fractions

  12. Workplace aerosol mass concentration measurement using optical particle counters.

    PubMed

    Görner, Peter; Simon, Xavier; Bémer, Denis; Lidén, Göran

    2012-02-01

    Direct-reading aerosol measurement usually uses the optical properties of airborne particles to detect and measure particle concentration. In the case of occupational hygiene, mass concentration measurement is often required. Two aerosol monitoring methods are based on the principle of light scattering: optical particle counting (OPC) and photometry. The former analyses the light scattered by a single particle, the latter by a cloud of particles. Both methods need calibration to transform the quantity of scattered light detected into particle concentration. Photometers are simpler to use and can be directly calibrated to measure mass concentration. However, their response varies not only with aerosol concentration but also with particle size distribution, which frequently contributes to biased measurement. Optical particle counters directly measure the particle number concentration and particle size that allows assessment of the particle mass provided the particles are spherical and of known density. An integrating algorithm is used to calculate the mass concentration of any conventional health-related aerosol fraction. The concentrations calculated thus have been compared with simultaneous measurements by conventional gravimetric sampling to check the possibility of field OPC calibration with real workplace aerosols with a view to further monitoring particle mass concentration. Aerosol concentrations were measured in the food industry using the OPC GRIMM® 1.108 and the CIP 10-Inhalable and CIP 10-Respirable (ARELCO®) aerosol samplers while meat sausages were being brushed and coated with calcium carbonate. Previously, the original OPC inlet had been adapted to sample inhalable aerosol. A mixed aerosol of calcium carbonate and fungi spores was present in the workplace. The OPC particle-size distribution and an estimated average particle density of both aerosol components were used to calculate the mass concentration. The inhalable and respirable aerosol fractions

  13. Organic Aerosols from SÃO Paulo and its Relationship with Aerosol Absorption and Scattering Properties

    NASA Astrophysics Data System (ADS)

    Artaxo, P.; Brito, J. F.; Rizzo, L. V.

    2012-12-01

    The megacity of São Paulo with its 19 million people and 7 million cars is a challenge from the point of view of air pollution. High levels of organic aerosols, PM10, black carbon and ozone and the peculiar situation of the large scale use of ethanol fuel makes it a special case. Little is known about the impact of ethanol on air quality and human health and the increase of ethanol as vehicle fuel is rising worldwide An experiment was designed to physico-chemical properties of aerosols in São Paulo, as well as their optical properties. Aerosol size distribution in the size range of 1nm to 10 micrometers is being measured with a Helsinki University SMPS (Scanning Mobility Particle Sizer), an NAIS (Neutral ion Spectrometer) and a GRIMM OPC (Optical Particle Counter). Optical properties are being measured with a TSI Nephelometer and a Thermo MAAP (Multi Angle Absorption Photometer). A CIMEL sunphotometer from the AERONET network measure the aerosol optical depth. Furthermore, a Proton-Transfer-Reaction Mass Spectrometer (PTR-MS) and an Aerosol Chemical Speciation Monitor (ACSM) are used to real-time VOC analysis and aerosol composition, respectively. The ACSM was operated for 3 months continuosly during teh wintertime of 2012. The measured total particle concentration typically varies between 10,000 and 30,000 cm-3 being the lowest late in the night and highest around noon and frequently exceeding 50,000 cm-3. Clear diurnal patterns in aerosol optical properties were observed. Scattering and absorption coefficients typically range between 20 and 100 Mm-1 at 450 nm, and between 10 to 40 Mm-1 at 637 nm, respectively, both of them peaking at 7:00 local time, the morning rush hour. The corresponding single scattering albedo varies between 0.50 and 0.85, indicating a significant contribution of primary absorbing particles to the aerosol population. During the first month a total of seven new particle formation events were observed with growth rates ranging from 9 to 25

  14. Particle Property Data Quality Flags for the MISR Aerosol Product

    NASA Astrophysics Data System (ADS)

    Gaitley, B. J.; Kahn, R. A.; Garay, M. J.

    2013-12-01

    The MISR instrument aboard the NASA Earth Observing System's Terra satellite has the unique capability to retrieve aerosol properties under favorable conditions. General aerosol type retrieval quality guidelines are provided in the MISR Data Quality Statement and related publications. The retrieved value of aerosol type is more sensitive to scene conditions than aerosol optical depth, and more difficult to validate, as there is very little coincident aerosol type validation data. Here we report on the steps we are taking to provide an aerosol-type data quality flag, to be provided with each individual retrieval result. Due to the lack of validation data for comparison, our main approach is to evaluate the self-consistency of aerosol type retrieval values for regions where particular aerosol types are known to dominate. Some factors affecting aerosol type retrieval quality that can be assessed pre-retrieval are the number of MISR cameras available, the range of scattering angles viewed, and surface conditions such as shallow water or seasonal coastal runoff. Factors that must be assessed post-retrieval include values of retrieved aerosol optical depth and the number and type of mixtures successfully passing the MISR algorithm acceptance criteria. Regional monthly plots with MISR measurements binned at 0.5 degree resolution and color-coded stratification of one or more parameters are the main tools for identifying locations and times where different aerosol types are retrieved. The statistics of individual MISR values such as mid-visible AOD, number and type of mixtures passing, number of cameras used, the range and maximum scattering angles, are studied as joint distributions on a region-by-region basis. From these, a synthesis of the self-consistency and agreement with expectation is made, effectively indicating the quality of the aerosol type constrains to the extent possible, and thresholds for assigning quality flags are assessed. Multiple-month summaries

  15. Analysis of aerosol scattering properties measured by a nephelometer at a coastal-rural site in the Atlantic southwest of the Iberian Peninsula

    NASA Astrophysics Data System (ADS)

    López, Juan F.; Cachorro, Victoria E.; de Frutos, Angel M.

    2015-09-01

    Aerosol hemispherical scattering and the backscattering coefficients, σsp, σbsc, have been measured using a 3-wavelength (450, 550 and 700 nm) integrating nephelometer over two years (January 2006-May 2008) in the coastal area of the Gulf of Cádiz, in the southwest of the Iberian Peninsula. These coefficients have been carefully analyzed starting with the impact of corrections on the measurements of σsp: i.e., drift calibration constants do not modify the mean value in our data series. However, the selection of dry data (with RH less than 50%) modifies substantially the number of data and the resulting mean value of σsp is now 14% lower, which is compensated when the angular truncation correction is applied. The characterization and features of σsp, σbsc, and the derived parameters αsp (alpha Ångström exponent) and b (the backscatter ratio) has been analyzed, as annual, seasonal and diurnal evolution. A general statistic based on hourly data gives mean values and standard deviation of σsp (500 nm)=48±38 Mm-1 with a median of 38 Mm-1, and σbsc (500 nm)=5.6±3.8 Mm-1 with a median of 4.6 Mm-1. Thus, these values show moderate-low values but with a large range of variation considering the existing measured values over the Iberian Peninsula. The median value of σsp (500 nm) is an indicator that events of high aerosol burden are frequent presenting a substantial influence on the daily averages. The alpha Ångström exponent, αsp, derived from the pairs 450/700 nm gives a mean value 1.35±0.54 with a median of 1.47 and with the most frequent value of 1.7, thus indicating the prevalence of medium size particles but with a significant influence of fine particles. The b ratio has the same value for mean and median, 0.12±0.02, showing a decrease with increasing values of σsp. Annual and daily cycles have been also analyzed showing the complex behaviour of the optical properties at this coastal site where cold and warn periods show very different

  16. Satellite Remote Sensing: Aerosol Measurements

    NASA Technical Reports Server (NTRS)

    Kahn, Ralph A.

    2013-01-01

    Aerosols are solid or liquid particles suspended in the air, and those observed by satellite remote sensing are typically between about 0.05 and 10 microns in size. (Note that in traditional aerosol science, the term "aerosol" refers to both the particles and the medium in which they reside, whereas for remote sensing, the term commonly refers to the particles only. In this article, we adopt the remote-sensing definition.) They originate from a great diversity of sources, such as wildfires, volcanoes, soils and desert sands, breaking waves, natural biological activity, agricultural burning, cement production, and fossil fuel combustion. They typically remain in the atmosphere from several days to a week or more, and some travel great distances before returning to Earth's surface via gravitational settling or washout by precipitation. Many aerosol sources exhibit strong seasonal variability, and most experience inter-annual fluctuations. As such, the frequent, global coverage that space-based aerosol remote-sensing instruments can provide is making increasingly important contributions to regional and larger-scale aerosol studies.

  17. The Cloud-Aerosol Transport System (CATS): Demonstrating New Techniques for Cloud and Aerosol Measurements

    NASA Astrophysics Data System (ADS)

    Yorks, J. E.; McGill, M. J.; Palm, S. P.; Hlavka, D. L.; Nowottnick, E. P.; Selmer, P. A.

    2015-12-01

    The Cloud-Aerosol Transport System (CATS) is an elastic backscatter lidar that provides vertical profiles of cloud and aerosol properties. The CATS payload has been operating since early February 2015 from the International Space Station (ISS). CATS was designed to operate for six months, and up to three years, providing a combination of operational science, in-space technology demonstration, and technology risk reduction for future Earth Science missions. One of the primary project goals of CATS is to demonstrate technology in support of future space-based lidar mission development. The CATS instrument has been demonstrating the high repetition rate laser and photon counting detection approach to lidar observations, in contrast to the low repetition rate, high energy technique employed by CALIPSO. Due to this technique, cloud and aerosol profile data exhibit high spatial and temporal resolution, which was never before possible from a space-based platform. Another important science goal of the CATS-FO project is accurate determination of aerosol type on a global scale. CATS provided the first space-based depolarization measurements at multiple wavelengths (532 and 1064 nm), and first measurements at 1064 nm from space. The ratio of the depolarization measurements at these two wavelengths enables significant improvement in aerosol typing. The CATS retrievals at 1064 nm also provide improvements to detecting aerosols above clouds. The CATS layer identification algorithm is a threshold-based layer detection method that uses the 1064 nm attenuated scattering ratio and also includes a routine to identify clouds embedded within aerosol layers. This technique allows CATS to detect the full extent of the aerosol layers above the cloud, and differentiate these two layers so that the optical properties can be more accurately determined.

  18. Aerosol optical properties and their radiative effects in northern China

    NASA Astrophysics Data System (ADS)

    Li, Zhanqing; Xia, Xiangao; Cribb, Maureen; Mi, Wen; Holben, Brent; Wang, Pucai; Chen, Hongbin; Tsay, Si-Chee; Eck, T. F.; Zhao, Fengsheng; Dutton, E. G.; Dickerson, R. E.

    2007-11-01

    As a fast developing country covering a large territory, China is experiencing rapid environmental changes. High concentrations of aerosols with diverse properties are emitted in the region, providing a unique opportunity for understanding the impact of environmental changes on climate. Until very recently, few observational studies were conducted in the source regions. The East Asian Study of Tropospheric Aerosols: An International Regional Experiment (EAST-AIRE) attempts to characterize the physical, optical and chemical properties of the aerosols and their effects on climate over China. This study presents some preliminary results using continuous high-quality measurements of aerosol, cloud and radiative quantities made at the first EAST-AIRE baseline station at Xianghe, about 70 km east of Beijing over a period of one year (September 2004 to September 2005). It was found that the region is often covered by a thick layer of haze (with a yearly mean aerosol optical depth equal to 0.82 at 500 nm and maximum greater than 4) due primarily to anthropogenic emissions. An abrupt "cleanup" of the haze often took place in a matter of one day or less because of the passage of cold fronts. The mean single scattering albedo is approximately 0.9 but has strong day-to-day variations with maximum monthly averages occurring during the summer. Large aerosol loading and strong absorption lead to a very large aerosol radiative effect at the surface (the annual 24-hour mean values equals 24 W m-2), but a much smaller aerosol radiative effect at the top of the atmosphere (one tenth of the surface value). The boundary atmosphere is thus heated dramatically during the daytime, which may affect atmospheric stability and cloud formation. In comparison, the cloud radiative effect at the surface is only moderately higher (-41 W m-2) than the aerosol radiative effect at the surface.

  19. Remote sensing measurements of biomass burning aerosol optical properties during the 2015 Indonesian burning season from AERONET and MODIS satellite data

    NASA Astrophysics Data System (ADS)

    2016-04-01

    The strong El Nino event in 2015 resulted in below normal rainfall leading to very dry conditions throughout Indonesia from August though October 2015. These conditions in turn allowed for exceptionally large numbers of biomass burning fires with very high emissions of aerosols. Over the island of Borneo, three AERONET sites (Palangkaraya, Pontianak, and Kuching) measured monthly mean fine mode aerosol optical depth (AOD) at 500 nm from the spectral deconvolution algorithm in September and October ranging from 1.6 to 3.7, with daily average AOD as high as 6.1. In fact, the AOD was sometimes too high to obtain any significant signal in the mid-visible wavelengths, therefore a previously developed new algorithm in the AERONET Version 3 database was invoked to retain the measurements in as many of the red and near-infrared wavelengths (675, 870, 1020, and 1640 nm) as possible to analyze the AOD in those wavelengths. These AOD at longer wavelengths are then utilized to provide some estimate the AOD in the mid-visible. Additionally, satellite retrievals of AOD at 550 nm from MODIS sensor data and the Dark Target, Beep Blue, and MAIAC algorithms were also analyzed and compared to AERONET measured AOD. Not surprisingly, the AOD was often too high for the satellite algorithms to also measure accurate AOD on many days in the densest smoke regions. The AERONET sky radiance inversion algorithm was utilized to analyze retrievals of the aerosol optical properties of complex refractive indices and size distributions. Since the AOD was often extremely high there was sometimes insufficient direct sun signal for the larger solar zenith angles (> 50 degrees) required for almucantar retrievals. However, the new hybrid sky radiance scan can attain sufficient scattering angle range even at small solar zenith angles when 440 nm direct beam irradiance can be accurately measured, thereby allowing for many more retrievals and also at higher AOD levels during this event. Due to extreme

  20. Aerosol pattern correlation techniques of wind measurement

    NASA Technical Reports Server (NTRS)

    Eloranta, Edwin W.

    1985-01-01

    This paper reviews the current status of lidar image correlation techniques of remote wind measurement. It also examines the potential use of satellite borne lidar global wind measurements using this approach. Lidar systems can easily detect spatial variations in the volume scattering cross section of naturally occurring aerosols. Lidar derived RHI, PPI and range-time displays of aerosol backscatter have been extensively employed in the study of atmospheric structure. Descriptions of this type of data can be obtained in many references including Kunkel et al. (1977), Kunkel et al. (1980), Boers et al. (1984), Uthe et al. (1980), Melfi et al. (1985) and Browell et al. (1983). It is likely that the first space-borne lidars for atmospheric studies will observe aerosol backscatter to measure parameters such as boundary layer depth and cloud height. This paper examines the potential application of these relatively simple aerosol backscatter lidars to global wind measurements.

  1. Studying Taklamakan aerosol properties with lidar (STAPL)

    NASA Astrophysics Data System (ADS)

    Cottle, Paul; Mueller, Detlef; Shin, Dong-Ho; Zhang, Xiao Xiao; Feng, Guanglong; McKendry, Ian; Strawbridge, Kevin

    2013-10-01

    By now, the global impacts of atmospheric dust have been well-established. Nevertheless, relevant properties such as size distribution, depolarization ratio, and even single-scattering albedo have been shown to vary substantially between dust producing regions and are also strongly dependant on the conditions under which the dust is emitted. Even greater variations have been documented during the process of long-range transport. With continued improvement of detection technologies, research focus is increasingly turning to refinement of our knowledge of these properties of dust in order to better account for the presence of dust in models and data analysis. The purpose of this study is to use a combination of lidar data and models to directly observe the changing properties of dust layers as they are transported from their origin in the Taklamakan Desert of western China. With the co-operation of the Xinjiang Institute of Ecology and Geography, a portable micropulse lidar system was installed at Aksu National Field on the northern edge of the Tarim Basin in late April 2013, during the Spring dust storm season. Over six days, data were collected on the optical properties of dust emissions passing over this location. The measurements of this lidar have shown the dust over Aksu on these days to have a significantly higher depolarization ratio than has been previously reported for the region. Model results show this dust was then transported across the region at least as far as Korea and Japan. Models from the Naval Aerosol Analysis and Prediction System (NAAPS) show that during transport the dust layers became intermixed with sulfate emissions from industrial sources in China as well as smoke from wildfires burning in south-east Asia and Siberia. The multi-wavelength raman-elastic lidar located in Gwangju South Korea was used to observe the vertical structure of the layers as well as optical properties such as colour ratio, depolarization ratio and extinction

  2. Optical Properties of Polymers Relevant to Secondary Organic Aerosols

    NASA Astrophysics Data System (ADS)

    Marrero-Ortiz, W.; Gomez-Hernandez, M. E.; Xu, W.; Guo, S.; Zhang, R.

    2014-12-01

    Atmospheric aerosols play a critical role in climate directly by scattering and absorbing solar radiation and indirectly by modifying the cloud formation. Currently, the direct and indirect effects of aerosols represent the largest uncertainty in climate predictions models. Some aerosols are directly emitted, but the majority are formed in the atmosphere by the oxidation of gaseous precursors. However, the formation of aerosols at the molecular level is not fully characterized. Certain category of secondary organic aerosols (SOA), which represent a significant fraction of the total aerosol burden, can be light-absorbing, also known as brown carbon. However, the overall contribution of SOA to the brown carbon and the related climate forcing is poorly understood. Such incomplete understanding is due in part to the chemical complexity of SOA and the lack of knowledge regarding SOA formation, transformation, and optical properties. Based on previous laboratory experiments, field measurements, and modeling studies, it has been suggested that the polymers and oligomers play an important role in the SOA formation. Atmospheric polymers could be produced by the hydration or heterogeneous reactions of epoxides and small α-dicarbonyls. Their aqueous chemistry products have been shown to give light-absorbing and high molecular weight oligomeric species, which increase the SOA mass production and alter the direct and indirect effect of aerosols. In this paper, the aerosol chemistry of small α-dicarbonyl compounds with amines is investigated and the associated optical properties are measured using spectroscopic techniques. The differences between primary, secondary and tertiary amines with glyoxal and methylglyoxal are evaluated in terms of SOA browning efficiency. Atmospheric implications of our present work for understanding the formation of light-absorbing SOA will be presented, particularly in terms of the product distribution of light-absorbing SOA formed by aqueous phase

  3. Global Aerosol Radiative Forcing Derived from Sea WiFS-Inferred Aerosol Optical Properties

    NASA Technical Reports Server (NTRS)

    Chou, Ming-Dah; Chan, Pui-King; Wang, Menghua

    1999-01-01

    Aerosol optical properties inferred from the Sea-viewing Wide Field-of-view Sensor (SeaWiFS) radiance measurements are used to compute the aerosol shortwave radiative forcing using a radiative transfer model. The aerosol optical thickness at the wavelength of 865-nm is taken from the SeaWIFS archive. It is found that the nominal optical thickness over oceans ranges from 0.1 to 0.2. Using a maritime aerosol model and the radiances measured at the various SeaWiFS channels, the Angstrom exponent is determined to be 0.2174, the single-scattering albedo to be 0.995, and the asymmetry factor to be 0.786. The radiative transfer model has eight bands in the visible and ultraviolet spectral regions and three bands in the near infrared. It includes the absorption due to aerosols, water vapor, carbon dioxide, and oxygen, and the scattering due to aerosols and gases (Rayleigh scattering). The radiative forcing is computed over global oceans for four months (January, April, July, and October, 1998) to represent four seasons. It is found that the aerosol radiative forcing is large and changes significantly with seasons near the continents with large-scale forest fires and desert dust. Averaged over oceans and the four months, the aerosol radiative forcing is approximately 7 W/sq m at the top of the atmosphere. This large radiative forcing is expected to have a significant cooling effect on the Earth's climate as implied from simulations of a number of general circulation models.

  4. 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.

  5. The investigation of advanced remote sensing techniques for the measurement of aerosol characteristics

    NASA Technical Reports Server (NTRS)

    Deepak, A.; Becher, J.

    1979-01-01

    Advanced remote sensing techniques and inversion methods for the measurement of characteristics of aerosol and gaseous species in the atmosphere were investigated. Of particular interest were the physical and chemical properties of aerosols, such as their size distribution, number concentration, and complex refractive index, and the vertical distribution of these properties on a local as well as global scale. Remote sensing techniques for monitoring of tropospheric aerosols were developed as well as satellite monitoring of upper tropospheric and stratospheric aerosols. Computer programs were developed for solving multiple scattering and radiative transfer problems, as well as inversion/retrieval problems. A necessary aspect of these efforts was to develop models of aerosol properties.

  6. Retrieval of aerosol optical properties over land using PMAp

    NASA Astrophysics Data System (ADS)

    Grzegorski, Michael; Munro, Rosemary; Lang, Ruediger; Poli, Gabriele; Holdak, Andriy

    2015-04-01

    The retrieval of aerosol optical properties is an important task for industry and climate forecasting. An ideal instrument should include observations with moderate spectral and high spatial resolutions for a wide range of wavelengths (from the UV to the TIR), measurements of the polarization state at different wavelengths and measurements of the same scene for different observation geometries. As such an ideal instrument is currently unavailable the usage of different instruments on one satellite platform is an alternative choice. Since February 2014, the Polar Multi sensor Aerosol product (PMAp) is delivered as operational GOME product to our customers. The algorithms retrieve aerosol optical properties over ocean (AOD, volcanic ash, aerosol type) using a multi-sensor approach (GOME, AVHRR, IASI). The next releases of PMAp will provide an extended set of aerosol and cloud properties which include AOD over land and an improved volcanic ash retrieval combining AVHRR and IASI. This presentation gives an overview on the existing product and the prototypes in development. The major focus is the discussion of the AOD retrieval over land implemented in the upcoming PMAp2 release. In addition, the results of our current validation studies (e.g. comparisons to AERONET, other satellite platforms and model data) are shown.

  7. 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.

  8. Measuring Sodium Chloride Contents of Aerosols

    NASA Technical Reports Server (NTRS)

    Sinha, M. P.; Friedlander, S. K.

    1986-01-01

    Amount of sodium chloride in individual aerosol particles measured in real time by analyzer that includes mass spectrometer. Analyzer used to determine mass distributions of active agents in therapeutic or diagnostic aerosols derived from saline solutions and in analyzing ocean spray. Aerosol particles composed of sodium chloride introduced into oven, where individually vaporized on hot wall. Vapor molecules thermally dissociated, and some of resulting sodium atoms ionized on wall. Ions leave oven in burst and analyzed by spectrometer, which is set to monitor sodium-ion intensity.

  9. Physical and Chemical Properties of Anthropogenic Aerosols: An overview

    EPA Science Inventory

    A wide variety of anthropogenic sources emit fine aerosols to the atmosphere. The physical and chemical properties of these aerosols are of interest due to their influence on climate, human health, and visibility. Aerosol chemical composition is complex. Combustion aerosols can c...

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

    SciTech Connect

    Paulson, S E

    2012-05-30

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

  11. The CU 2-D-MAX-DOAS instrument – Part 2: Raman scattering probability measurements and retrieval of aerosol optical properties

    DOE PAGES

    Ortega, Ivan; Coburn, Sean; Berg, Larry K.; Lantz, Kathy; Michalsky, Joseph; Ferrare, Richard A.; Hair, Johnathan W.; Hostetler, Chris A.; Volkamer, Rainer

    2016-08-23

    The multiannual global mean of aerosol optical depth at 550 nm (AOD550) over land is ∼ 0.19, and that over oceans is ∼ 0.13. About 45 % 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. We present an inherently calibrated retrieval (i.e., no need for radiance calibration) to simultaneously measure AOD and the aerosol phase function parameter, g, based on measurements of azimuth distributions of the Raman scattering probability (RSP), the near-absolute rotational Raman scattering (RRS) intensity. We employ radiative transfer model simulations tomore » show that for solar azimuth RSP measurements at solar elevation and solar zenith angle (SZA) smaller than 80°, RSP is insensitive to the vertical distribution of aerosols and maximally sensitive to changes in AOD and g under near-molecular scattering conditions. The University of Colorado two-dimensional Multi-AXis Differential Optical Absorption Spectroscopy (CU 2-D-MAX-DOAS) instrument was deployed as part of the Two Column Aerosol Project (TCAP) at Cape Cod, MA, during the summer of 2012 to measure direct sun spectra and RSP from scattered light spectra at solar relative azimuth angles (SRAAs) between 5 and 170°. During two case study days with (1) high aerosol load (17 July, 0.3  <  AOD430 < 0.6) and (2) near-molecular scattering conditions (22 July, AOD430 < 0.13) we compare RSP-based retrievals of AOD430 and g with data from a co-located CIMEL sun photometer, Multi-Filter Rotating Shadowband Radiometer (MFRSR), and an airborne High Spectral Resolution Lidar (HSRL-2). The average difference (relative to DOAS) for AOD430 is +0.012 ± 0.023 (CIMEL), −0.012 ± 0.024 (MFRSR), −0.011 ± 0.014 (HSRL-2), and +0.023 ± 0.013 (CIMELAOD − MFRSRAOD) and yields the following expressions for correlations between different instruments

  12. Global dust infrared aerosol properties retrieved using hyperspectral sounders

    NASA Astrophysics Data System (ADS)

    Capelle, Virginie; Chédin, alain; Pondrom, Marc; Pierangelo, Clémence; Armante, Raymond; Crevoisier, Cyril; Crépeau, Laurent; Scott, Noëlle

    2015-04-01

    Observations from infrared hyperspectral sounders, here IASI and AIRS, are interpreted in terms of dust aerosol properties (AOD and mean altitude). The method is based on a "Look-Up-Table" (LUT) approach, where all radiative transfer computation is performed once for all and "off-line", for a large selection of atmospheric situations, of observing conditions, of surface characteristics (in particular the surface emissivity and temperature), and different aerosol refractive index models. The inversion scheme follows two main steps: first, determination of the observed atmospheric thermodynamic situation, second, simultaneous retrieval of the 10µm coarse-mode AOD and of the mean altitude. The method is here applied over sea and over land, at daily scale daytime and nighttime, and at the satellite pixel resolution (12 km at nadir). The geographical study area studied includes the northern tropics from west Atlantic to the Arabian peninsula and Indian ocean, and the Mediterranean basin, all of them characterized by strong, regular dust events. A special focus is given to the hourly variation of aerosol properties within a day. In this context, both IASI overpasses are processed, providing two measurements at 9:30AM and 9:30PM (equator local time) each day. First results obtained from AIRS observations, made at 1:30 AM and PM, open the way to the analysis of the aerosol diurnal cycle. For the AOD, comparisons are made with AERONET ground-based data , when available, in order to 1) evaluate our results, and 2) show the importance of a better knowledge of the aerosol diurnal cycle, especially close to the sources. Mean aerosol layer altitude obtained from IASI is compared at local scale with the Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP/CALIPSO) aerosol altitude.

  13. Optical Properties of Atmospheric Aerosol in Maritime Environments.

    NASA Astrophysics Data System (ADS)

    Smirnov, Alexander; Holben, Brent N.; Kaufman, Yoram J.; Dubovik, Oleg; Eck, Thomas F.; Slutsker, Ilya; Pietras, Christophe; Halthore, Rangasayi N.

    2002-02-01

    Systematic characterization of aerosol over the oceans is needed to understand the aerosol effect on climate and on transport of pollutants between continents. Reported are the results of a comprehensive optical and physical characterization of ambient aerosol in five key island locations of the Aerosol Robotic Network (AERONET) of sun and sky radiometers, spanning over 2-5 yr. The results are compared with aerosol optical depths and size distributions reported in the literature over the last 30 yr. Aerosol found over the tropical Pacific Ocean (at three sites between 20°S and 20°N) still resembles mostly clean background conditions dominated by maritime aerosol. The optical thickness is remarkably stable with mean value of a(500 nm) = 0.07, mode value at am = 0.06, and standard deviation of 0.02-0.05. The average Ångström exponent range, from 0.3 to 0.7, characterizes the wavelength dependence of the optical thickness. Over the tropical to subtropical Atlantic (two stations at 7°S and 32°N) the optical thickness is significantly higher: a(500 nm) = 0.14 and am = 0.10 due to the frequent presence of dust, smoke, and urban-industrial aerosol. For both oceans the atmospheric column aerosol is characterized by a bimodal lognormal size distribution with a fine mode at effective radius Reff = 0.11 ± 0.01 m and coarse mode at Reff = 2.1 ± 0.3 m. A review of the published 150 historical ship measurements from the last three decades shows that am was around 0.07 to 0.12 in general agreement with the present finding. The information should be useful as a test bed for aerosol global models and aerosol representation in global climate models. With global human population expansion and industrialization, these measurements can serve in the twenty-first century as a basis to assess decadal changes in the aerosol concentration, properties, and radiative forcing of climate.

  14. THERMAL PROPERTIES OF SECONDARY ORGANIC AEROSOLS

    EPA Science Inventory

    Volume concentrations of steady-state secondary organic aerosol (SOA) were measured in several hydrocarbon/NOx irradiation experiments. These measurements were used to estimate the thermal behavior of the particles that may be formed in the atmosphere. These laborator...

  15. Practical application of in situ aerosol measurement

    SciTech Connect

    O`Hern, T.J.; Rader, D.J.

    1993-09-01

    The use of in situ, real-time measurement techniques permits the characterization of airborne droplets and particles under conditions where traditional sampling methods can fail. For example, sampling method rely on the ability to sample and transport particles without biasing the properties of interest, and often are not applicable in harsh environment. Although in situ methods offer unique opportunities in these cases, these techniques introduce new concerns and must be used carefully if accurate measurement are to be made. Several in situ measurement techniques are reviewed here. As the field is rapidly evolving, the discussion is limited to those techniques which: (1) are commercially available, (2) provide real-time output, (3) measure the aerosol size distribution. Discussion is divided between single particle counters (which provide a flux-based or temporal measurement) and ensemble techniques (which provide a concentration-based or spatial measurement). Specific techniques discussed include phase Doppler, Mie scattering, and Fraunhofer diffraction, and commercial instruments based on these techniques.

  16. Novel Measurements of Aerosol Particle Interfaces Using Biphasic Microfluidics

    NASA Astrophysics Data System (ADS)

    Metcalf, A. R.; Dutcher, C. S.

    2014-12-01

    Secondary organic aerosol (SOA) particles are nearly ubiquitous in the atmosphere and yet there remains large uncertainties in their formation processes and ambient properties. These particles are complex microenvironments, which can contain multiple interfaces due to internal aqueous-organic phase partitioning and to the external liquid-vapor surface. These aerosol interfaces can profoundly affect the fate of condensable organic compounds emitted into the atmosphere by altering the way in which organic vapors interact with the ambient aerosol. Aerosol interfaces affect particle internal structure, species uptake, equilibrium partitioning, activation to cloud condensation or ice nuclei, and optical properties. For example, organic thin films can shield the core of the aerosol from the ambient environment, which may disrupt equilibrium partitioning and mass transfer. To improve our ability to accurately predict the fate of SOA in the atmosphere, we must improve our knowledge of aerosol interfaces and their interactions with the ambient environment. Few technologies exist to accurately probe aerosol interfaces at atmospherically-relevant conditions. In this talk, a novel method using biphasic microscale flows will be introduced for generating, trapping, and perturbing complex interfaces at atmospherically relevant conditions. These microfluidic experiments utilize high-speed imaging to monitor interfacial phenomena at the microscale and are performed with phase contrast and fluorescence microscopy on a temperature-controlled inverted microscope stage. From these experiments, interfacial thermodynamic properties such as surface tension, rheological properties such as interfacial moduli, and kinetic properties such as mass transfer coefficients can be measured or inferred. Chemical compositions of the liquid phases studied here span a range of viscosities and include electrolyte and water soluble organic acid species often observed in the atmosphere, such as mixtures

  17. Properties of Stratospheric Aerosol Estimated from HALOE Data

    NASA Technical Reports Server (NTRS)

    Lee, Kwang-Mog; Park, Jae H.; Massie, Steven T.; Choi, Wookap

    2001-01-01

    Extinction coefficients for stratospheric aerosols at 8 HALOE (HALogen Occultation Experiment) wavelengths are determined by comparing transmittances data for two adjacent solar occultation measurements, where one limb path is loaded with aerosols but the other path is free of aerosols. These extinction coefficients are used to infer the aerosol properties such as composition and size distribution parameters. Mie theory has been used to calculate the extinction coefficients, and a nonlinear least square method is applied to determine the aerosol properties. Sixteen cases are selected for the retrieval in southern hemisphere at latitudes from 21 to 48 deg S for the period of 29 Mar - 31 May 1992. Retrieved size width ranges from 1.1 to 1.5 and radius ranges from 0.25 to 0.45 micrometers. These size parameters are within the ranges of in situ measurements at Laramie, Wyoming. Retrieved weight percent of H2SO4 is larger than the equilibrium value by about 5 to approximately 10 weight percent, similar to the results for northern hemisphere at latitudes 20 to 55 deg N for the period from Nov 1991 to Feb. 1992.

  18. Optical Properties of Black and Brown Carbon Aerosols from Laboratory Combustion of Wildland Fuels

    NASA Astrophysics Data System (ADS)

    Beres, N. D.; Molzan, J.

    2015-12-01

    Aerosol light absorption in the solar spectral region (300 nm - 2300 nm) of the atmosphere is key for the direct aerosol radiative forcing, which is determined by aerosol single scattering albedo (SSA), asymmetry parameter, and by the albedo of the underlying surface. SSA is of key importance for the sign and quantity of aerosol direct radiative forcing; that is, does the aerosol make the earth look darker (heating) or whiter (cooling)? In addition, these optical properties are needed for satellite retrievals of aerosol optical depth and properties. During wildland fires, aerosol optical absorption is largely determined by black carbon (BC) and brown carbon (BrC) emissions. BC is strongly absorbing throughout the solar spectrum, while BrC absorption strongly increases toward shorter wavelength and can be neglected in the red and infrared. Optical properties of BrC emitted from wildland fires are poorly understood and need to be studied as function of fuel type and moisture content and combustion conditions. While much more is known about BC optical properties, knowledge for the ultraviolet (UV) spectral region is still lacking and critically needed for satellite remote sensing (e.g., TOMS, OMI) and for modeling of tropospheric photochemistry. Here, a project to better characterize biomass burning aerosol optical properties is described. It utilizes a laboratory biomass combustion chamber to generate aerosols through combustion of different wildland fuels of global and regional importance. Combustion aerosol optics is characterized with an integrating nephelometer to measure aerosol light scattering and a photoacoustic instrument to measure aerosol light absorption. These measurements will yield optical properties that are needed to improve qualitative and quantitative understanding of aerosol radiative forcing and satellite retrievals for absorbing carbonaceous aerosols from combustion of wildland fuels.

  19. Estimate of the aerosol properties over the ocean with POLDER

    NASA Astrophysics Data System (ADS)

    Deuzé, J. L.; Goloub, P.; Herman, M.; Marchand, A.; Perry, G.; Susana, S.; Tanré, D.

    2000-06-01

    The wide field of view imaging spectroradiometer Polarization and Directionality of the Earth's Reflectance (POLDER) developed by Centre National d'Etudes Spatiales and operated aboard the Japanese heliosynchronous platform Advanced Earth Observation Satellite (ADEOS) from October 30, 1996, to June 30, 1997, provided the first global systematic measurements of the spectral, directional, and polarized characteristics of the solar radiation reflected by the Earth/atmosphere system. These original observational capabilities offer an opportunity to enhance the characterization of several components of the global environment, especially the oceanic and terrestrial vegetal primary production, the aerosol physical and optical properties, and the tridimensional structure and microphysics of clouds. Here we examine the remote sensing of aerosols over the oceans. In a first step the aerosol optical thickness and Ångström exponent are derived from the radiance measurements. In a second step the polarization measurements are used for the retrieval of the aerosol refractive index. The inversion algorithm assumes spherical, nonabsorbing particles with monomodal lognormal size distribution. The adequacy of this modeling is discussed for a representative set of aerosol observations. Successful retrieval is generally achieved in the presence of small aerosols with Ångström exponent larger than ˜1.0. For such particles, polarization may provide information on the particle refractive index. As the Ångstrom exponent of the particle decreases, the data fitting residual errors increase, especially in polarized light, which prevents the retrieval of the aerosol refractive index. The trends of the discrepancies point out two shortcomings of the aerosol modeling. The theoretical results systematically underestimate the contribution of small polarizing particles in the polarization measurements for side-scattering angles ranging from 80° to 120°. This indicates very probably that

  20. Impact of particle nonsphericity on the development and properties of aerosol models for East Asia

    NASA Astrophysics Data System (ADS)

    Chen, Hao; Cheng, Tianhai; Gu, Xingfa; Wu, Yu

    2015-01-01

    In this paper, the effects of aerosol nonsphericity information on the classification of aerosol models and the associated radiative properties over East Asia are investigated. The radiance measurements and inversions of the Aerosol Robotic Network (AERONET) are used. Four aerosol models over East Asia are obtained by adding the shape information to the clustering analysis. These four aerosols are identified on the basis of their optical properties. Compared to the results without sphericity parameter, adding the sphericity parameter in the clustering process contributes to the extraction of a strongly absorbing aerosol. Furthermore, the effect of the physical and optical properties of the aerosol on the top of atmospheric (TOA) total reflectance and polarized reflectance are investigated. The results indicate that the addition of the sphericity parameter in the clustering process leads to a change in the total reflectance by up to 16% and a change in the polarized reflectance by up to 100%.

  1. The spatial-temporal variations in optical properties of atmosphere aerosols over China and its application in remote sensing

    NASA Astrophysics Data System (ADS)

    Chen, H.; Cheng, T.

    2013-12-01

    The atmospheric and climate response to the aerosol forcing are assessed by climate models regionally and globally under the past, present and future conditions. However, large uncertainties exist because of incomplete knowledge concerning the distribution and the physical and chemical properties of aerosols as well as aerosol-cloud interactions. Reduction in these uncertainties requires long-term monitoring of detailed properties of different aerosol types. China is one of the heavily polluted areas with high concentration of aerosols in the world. The complex source, composition of China aerosol led to the worse accuracy of aerosol radiative forcing assessment in the world, which urgently calls for improvements on the understanding of China regional aerosol properties. The spatial-temporal properties of aerosol types over China are studied using the radiance measurements and inversions data at 4 Aerosol Robotic Network (AERONET) stations. Five aerosol classes were identified including a coarse-size dominated aerosol type (presumably dust) and four fine-sized dominated aerosol types ranging from non-absorbing to highly absorbing fine aerosols. The mean optical properties of different aerosol types in China and their seasonal variations were also investigated. Based on the cluster analysis, the improved ground-based aerosol model is applied to the MODIS dark target inversion algorithm. Validation with MODIS official product and CE318 is also included.

  2. Aerosol properties over Interior Alaska from lidar, DRUM Impactor sampler, and OPC-sonde measurements and their meteorological context during ARCTAS-A, April 2008

    NASA Astrophysics Data System (ADS)

    Atkinson, D. E.; Sassen, K.; Hayashi, M.; Cahill, C. F.; Shaw, G.; Harrigan, D.; Fuelberg, H.

    2013-02-01

    Aerosol loading over Interior Alaska displays a strong seasonality, with pristine conditions generally prevailing during winter months. Long term aerosol research from the University of Alaska Fairbanks indicates that the period around April typically marks the beginning of the transition from winter to summer conditions. In April 2008, the NASA-sponsored "Arctic Research of the Composition of the Troposphere from Aircraft and Satellites" (ARCTAS) field campaign was conducted to analyze incursions of aerosols transported over Alaska and the Canadian North. In and around Fairbanks, Alaska, data concerning aerosol characteristics were gathered by polarization (0.693 μm) lidar, DRUM Impactor sampler, and balloon-borne optical particle counter. These data provide information on the vertical distribution and type of aerosol, their size distributions, the chemical nature of aerosol observed at the surface, and timing of aerosol loading. A detailed synoptic analysis placed these observations into their transport and source-region context. Evidence suggests four major aerosol loading periods in the 25 March-30 April 2008 timeframe: a period during which typical Arctic haze conditions prevailed, several days of extremely clear conditions, rapid onset of a period dominated by Asian dust with some smoke, and a period dominated by Siberian wildfire smoke. A focused case study analysis conducted on 19 April 2008 using a balloon-borne optical particle counter suggests that, on this day, the majority of the suspended particulate matter consisted of coarse mode desiccated aerosol having undergone long-range transport. Backtrack trajectory analysis suggests aged Siberian wildfire smoke. In the last week of April, concentrations gradually decreased as synoptic conditions shifted away from favoring transport to Alaska. An important result is a strong suggestion of an Asian dust incursion in mid-April that was not well identified in other ARCTAS measurements. The lidar and OPC

  3. Optical measurement of medical aerosol media parameters

    NASA Astrophysics Data System (ADS)

    Sharkany, Josif P.; Zhytov, Nikolay B.; Sichka, Mikhail J.; Lemko, Ivan S.; Pintye, Josif L.; Chonka, Yaroslav V.

    2000-07-01

    The problem of aerosol media parameters measurements are presented in the work and these media are used for the treatment of the patients with bronchial asthma moreover we show the results of the development and the concentration and dispersity of the particles for the long-term monitoring under such conditions when the aggressive surroundings are available. The system for concentration measurements is developed, which consists of two identical photometers permitting to carry out the measurements of the transmission changes and the light dispersion depending on the concentration of the particles. The given system permits to take into account the error, connected with the deposition of the salt particles on the optical windows and the mirrors in the course of the long-term monitoring. For the controlling of the dispersity of the aggressive media aerosols the optical system is developed and used for the non-stop analysis of the Fure-spectra of the aerosols which deposit on the lavsan film. The registration of the information is performed with the help of the rule of the photoreceivers or CCD-chamber which are located in the Fure- plane. With the help of the developed optical system the measurements of the concentration and dispersity of the rock-salt aerosols were made in the medical mines of Solotvino (Ukraine) and in the artificial chambers of the aerosol therapy.

  4. ELECTRICAL AEROSOL DETECTOR (EAD) MEASUREMENTS AT THE ST. LOUIS SUPERSITE

    EPA Science Inventory

    The Model 3070A Electrical Aerosol Detector (EAD) measures a unique aerosol parameter called total aerosol length. Reported as mm/cm3, aerosol length can be thought of as a number concentration times average diameter, or simply as d1 weighting. This measurement falls between nu...

  5. Evaluation of aerosol properties simulated by the high resolution global coupled chemistry-aerosol-microphysics model C-IFS-GLOMAP

    NASA Astrophysics Data System (ADS)

    Dhomse, Sandip; Mann, Graham; Carslaw, Ken; Flemming, Johannes; Morcrette, Jean-Jacques; Engelen, Richard; Remy, Samuel; Boucher, Olivier; Benduhn, Francois; Hewson, Will; Woodhouse, Matthew

    2016-04-01

    The EU Framework Programme GEMS and MACC consortium projects co-ordinated by the European Centre for Medium-range Weather Forecasts (ECMWF) have developed an operational global forecasting and reanalysis system (Composition-IFS) for atmospheric composition including greenhouse gases, reactive gases and aerosol. The current operational C-IFS system uses a mass-based aerosol model coupled to data assimilation of Aerosol Optical Depth measured by satellite (MODIS) to predict global aerosol properties. During MACC, the GLOMAP-mode aerosol microphysics scheme was added to the system, providing information on aerosol size and number for improved representation of aerosol-radiation and aerosol-cloud interactions, accounting also for simulated global variations in size distribution and internally-mixed particle composition. The IFS-GLOMAP system has recently been upgraded to couple with the sulphur cycle simulated in the online TM5 tropospheric chemistry module for global reactive gases. This C-IFS-GLOMAP system is also being upgraded to use a new "nitrate-extended" version of GLOMAP which realistically treats the size-resolved gas-particle partitioning of semi volatile gases ammonia and nitric acid. In this poster we described C-IFS-GLOMAP and present an evaluation of the global sulphate aerosol distribution simulated in this coupled aerosol-chemistry C-IFS-GLOMAP, comparing to surface observations in Europe, North America and the North Atlantic and contrasting to the fixed timescale sulphate production scheme developed in GEMS. We show that the coupling to the TM5 sulphur chemistry improves the seasonal cycle of sulphate aerosol, for example addressing a persistent wintertime sulphate high bias in northern Europe. The improved skill in simulated sulphate aerosol seasonal cycle is a pre-requisite to realistically characterise nitrate aerosol since biases in sulphate affect the amount of free ammonia available to form ammonium nitrate.

  6. Evaluations of tropospheric aerosol properties simulated by the community earth system model with a sectional aerosol microphysics scheme

    PubMed Central

    Toon, Owen B.; Bardeen, Charles G.; Mills, Michael J.; Fan, Tianyi; English, Jason M.; Neely, Ryan R.

    2015-01-01

    Abstract A sectional aerosol model (CARMA) has been developed and coupled with the Community Earth System Model (CESM1). Aerosol microphysics, radiative properties, and interactions with clouds are simulated in the size‐resolving model. The model described here uses 20 particle size bins for each aerosol component including freshly nucleated sulfate particles, as well as mixed particles containing sulfate, primary organics, black carbon, dust, and sea salt. The model also includes five types of bulk secondary organic aerosols with four volatility bins. The overall cost of CESM1‐CARMA is approximately ∼2.6 times as much computer time as the standard three‐mode aerosol model in CESM1 (CESM1‐MAM3) and twice as much computer time as the seven‐mode aerosol model in CESM1 (CESM1‐MAM7) using similar gas phase chemistry codes. Aerosol spatial‐temporal distributions are simulated and compared with a large set of observations from satellites, ground‐based measurements, and airborne field campaigns. Simulated annual average aerosol optical depths are lower than MODIS/MISR satellite observations and AERONET observations by ∼32%. This difference is within the uncertainty of the satellite observations. CESM1/CARMA reproduces sulfate aerosol mass within 8%, organic aerosol mass within 20%, and black carbon aerosol mass within 50% compared with a multiyear average of the IMPROVE/EPA data over United States, but differences vary considerably at individual locations. Other data sets show similar levels of comparison with model simulations. The model suggests that in addition to sulfate, organic aerosols also significantly contribute to aerosol mass in the tropical UTLS, which is consistent with limited data.

  7. Evaluations of tropospheric aerosol properties simulated by the community earth system model with a sectional aerosol microphysics scheme

    PubMed Central

    Toon, Owen B.; Bardeen, Charles G.; Mills, Michael J.; Fan, Tianyi; English, Jason M.; Neely, Ryan R.

    2015-01-01

    Abstract A sectional aerosol model (CARMA) has been developed and coupled with the Community Earth System Model (CESM1). Aerosol microphysics, radiative properties, and interactions with clouds are simulated in the size‐resolving model. The model described here uses 20 particle size bins for each aerosol component including freshly nucleated sulfate particles, as well as mixed particles containing sulfate, primary organics, black carbon, dust, and sea salt. The model also includes five types of bulk secondary organic aerosols with four volatility bins. The overall cost of CESM1‐CARMA is approximately ∼2.6 times as much computer time as the standard three‐mode aerosol model in CESM1 (CESM1‐MAM3) and twice as much computer time as the seven‐mode aerosol model in CESM1 (CESM1‐MAM7) using similar gas phase chemistry codes. Aerosol spatial‐temporal distributions are simulated and compared with a large set of observations from satellites, ground‐based measurements, and airborne field campaigns. Simulated annual average aerosol optical depths are lower than MODIS/MISR satellite observations and AERONET observations by ∼32%. This difference is within the uncertainty of the satellite observations. CESM1/CARMA reproduces sulfate aerosol mass within 8%, organic aerosol mass within 20%, and black carbon aerosol mass within 50% compared with a multiyear average of the IMPROVE/EPA data over United States, but differences vary considerably at individual locations. Other data sets show similar levels of comparison with model simulations. The model suggests that in addition to sulfate, organic aerosols also significantly contribute to aerosol mass in the tropical UTLS, which is consistent with limited data. PMID:27668039

  8. Space measurements of tropospheric aerosols

    NASA Technical Reports Server (NTRS)

    Griggs, M.

    1981-01-01

    A global-scale ground-truth experiment was conducted in the summer of 1980 with the AVHRR sensor on NOAA-6 to investigate the relationship between the upwelling visible radiance and the aerosol optical thickness over oceans at different sites around the globe. The possibility of using inland bodies of water such as rivers, lakes and reservoirs has been recently investigated using the Landsat MSS7 (approximately 0.9 micron) channel. This upwelling near-infrared radiance is less influenced than the visible radiance by the suspended matter generally found in the inland bodies of water, and by the adjacency effect of the surrounding higher albedo land. It is found that the water turbidity has more influence than the adjacency effect and reduces the effectiveness of the technique for inland observations.

  9. A study of remotely sensed aerosol properties from ground-based sun and sky scanning radiometers

    NASA Astrophysics Data System (ADS)

    Giles, David M.

    Aerosol particles impact human health by degrading air quality and affect climate by heating or cooling the atmosphere. The Indo-Gangetic Plain (IGP) of Northern India, one of the most populous regions in the world, produces and is impacted by a variety of aerosols including pollution, smoke, dust, and mixtures of them. The NASA Aerosol Robotic Network (AERONET) mesoscale distribution of Sun and sky-pointing instruments in India was established to measure aerosol characteristics at sites across the IGP and around Kanpur, India, a large urban and industrial center in the IGP, during the 2008 pre-monsoon (April-June). This study focused on detecting spatial and temporal variability of aerosols, validating satellite retrievals, and classifying the dominant aerosol mixing states and origins. The Kanpur region typically experiences high aerosol loading due to pollution and smoke during the winter and high aerosol loading due to the addition of dust to the pollution and smoke mixture during the pre-monsoon. Aerosol emissions in Kanpur likely contribute up to 20% of the aerosol loading during the pre-monsoon over the IGP. Aerosol absorption also increases significantly downwind of Kanpur indicating the possibility of the black carbon emissions from aerosol sources such as coal-fired power plants and brick kilns. Aerosol retrievals from satellite show a high bias when compared to the mesoscale distributed instruments around Kanpur during the pre-monsoon with few high quality retrievals due to imperfect aerosol type and land surface characteristic assumptions. Aerosol type classification using the aerosol absorption, size, and shape properties can identify dominant aerosol mixing states of absorbing dust and black carbon particles. Using 19 long-term AERONET sites near various aerosol source regions (Dust, Mixed, Urban/Industrial, and Biomass Burning), aerosol absorption property statistics are expanded upon and show significant differences when compared to previous work

  10. Modeling of aerosol properties related to direct climate forcing

    NASA Astrophysics Data System (ADS)

    Koloutsou-Vakakis, Sotiria; Rood, Mark J.; Nenes, Athanasios; Pilinis, Christodoulos

    1998-07-01

    A long-term local experiment was designed with the purpose to accurately quantify aerosol parameters needed in order to estimate aerosol climate forcing at an anthropogenically perturbed continental site. Total light-scattering σλ,sp and backscattering σλ,bsp coefficients at wavelength λ, the hygroscopic growth factors with respect to scattering, ƒ(RH)λ,s, and the backscatter ratio bλ are the parameters considered in the paper. Reference and controlled relative humidity nephelometry measurements were taken at a ground level field sampling station, located near Bondville Illinois (40°03'12″N, W 88°22'19″W). Aerosol particle chemical composition and mass particle size distributions were also measured. The target parameters were also estimated from models. The modeling approach involved a two-step process. In the first step, aerosol properties were parameterized with an approach that made use of a modified thermodynamic equilibrium model, published laboratory measurements of single hygroscopic particle properties, and empirical mixing rules. In the second step, the parameterized aerosol properties were used as inputs into a code that calculate σλ,sp and σλ,bsp as functions of λ, RH, particle size, and composition. Comparison between the measured and the modeled results showed that depending on the assumptions, the differences between the modeled and observed results were within 5 to 28% for ƒ(RH)λ,s and within 22-35% for bλ at low RH and 0-20% for bλ at high RH. The temporal variation of the particle size distribution, the equilibrium state of the particles, and the hygroscopicity of the material characterized as residual were the major factors limiting the predictive ability of the models.

  11. Retrieval of aerosol composition using ground-based remote sensing measurements

    NASA Astrophysics Data System (ADS)

    Xie, Yisong; Li, Zhengqiang; Zhang, Ying; Li, Donghui; Li, Kaitao

    2016-04-01

    The chemical composition and mixing states of ambient aerosol are the main factors deciding aerosol microphysical and optical properties, and thus have significant impacts on regional or global climate change and air quality. Traditional approaches to detect atmospheric aerosol composition include sampling with laboratory analysis and in-situ measurements. They can accurately acquire aerosol components, however, the sampling or air exhausting could change the status of ambient aerosol or lead to some mass loss. Additionally, aerosol is usually sampled at the surface level so that it is difficult to detect the columnar aerosol properties. Remote sensing technology, however, can overcome these problems because it is able to detect aerosol information of entire atmosphere by optical and microphysical properties without destructing the natural status of ambient aerosol. This paper introduces a method to acquire aerosol composition by the remote sensing measurements of CIMEL CE318 ground-based sun-sky radiometer. A six component aerosol model is used in this study, including one strong absorbing component Black Carbon (BC), two partly absorbing components Brown Carbon (BrC) and Mineral Dust (MD), two scattering components Ammonia Sulfate-like (AS) and Sea Salt (SS), and Aerosol Water uptake (AW). Sensitivity analysis are performed to find the most sensitive parameters to each component and retrieval method for each component is accordingly developed. Different mixing models such as Maxwell-Garnett (MG), Bruggeman (BR) and Volume Average (VA) are also studied. The residual minimization method is used by comparing remote sensing measurements and simulation outputs to find the optimization of aerosol composition (including volume fraction and mass concentration of each component). This method is applied to measurements obtained from Beijing site under different weather conditions, including polluted haze, dust storm and clean days, to investigate the impacts of mixing

  12. Retrieval of aerosol composition using ground-based remote sensing measurements

    NASA Astrophysics Data System (ADS)

    Xie, Y.; Li, Z.; Xu, H.; Chen, X.; Li, K.; Lv, Y.; Li, D.; Zhang, Y.

    2015-12-01

    The chemical composition and mixing status of ambient aerosol are the main factors deciding aerosol microphysical and optical properties, and thus have significant impacts on regional or global climate change and air quality. Traditional approaches to detect atmospheric aerosol composition include sampling with laboratory analysis and in-situ measurement. They can accurately acquire aerosol components, however, the sampling or air exhausting could change the status of aerosol or have some mass loss. Additionally, aerosol is usually sampled at the surface level so that it is difficult to detect the columnar aerosol properties. Remote sensing technology, however, can overcome these problems because it investigate aerosol information by optical and microphysical properties without destructing the natural status of ambient aerosol. This paper introduce a method to acquire aerosol composition by the remote sensing measurements of CIMEL CE318 ground-based sun-sky radiometer. A six component aerosol model is used in this study, including one strong absorbing component Black Carbon (BC), two partly absorbing components Brown Carbon (BrC) and Mineral Dust (MD), two scattering components Ammonia Sulfate-like (AS) and Sea Salt (SS), and Aerosol Water uptake (AW). Sensitivity analysis are performed to find the most sensitive parameters to each component and retrieval method for each component is accordingly developed. The residual minimization method is used by comparing remote sensing measurements and simulation outputs to find the optimization of aerosol composition (including volume fraction and mass concentration of each component). This method is applied to real measurements obtained from Beijing site under different weather conditions, including polluted haze, dust storm and clean days, to investigate the impacts of mixing states of aerosol particles on aerosol composition retrieval.

  13. 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.

  14. Sarychev Volcanic Aerosol and Chemical measurements over Eureka, Canada

    NASA Astrophysics Data System (ADS)

    Perro, C. W.; Duck, T. J.; Bitar, L.; Nott, G. J.; Lesins, G. B.; O'Neill, N. T.; Eloranta, E.; Strong, K.; Carn, S. A.; Lindenmaier, R.; Batchelor, R.; Saha, A.; Pike-Thackray, C.; Drummond, J. R.

    2010-12-01

    On July 01, 2009, lidar measurements from Eureka, Canada (80°N, 85°W) detected unusually high amounts of aerosol in the lower stratosphere which are believed to have originated from the Sarychev Eruption on the Kuril Islands in Russia (48°N,153°E). The suite of instruments that are part of the Canadian Network for the Detection of Atmospheric Change (CANDAC) have been used to measure the optical and chemical properties of the volcanic plume over Eureka. Lidar measurements show significant structure in the stratospheric aerosol that reaches altitudes of approximately 17 km. Initially there were several layers of aerosol in the lower stratosphere, which began to mix vertically so that by the end of August the aerosol was mixed into one homogeneous layer in the lower stratosphere. Lidar and sun photometer measurements are used to track the change in the integrated volume backscatter cross section from July 2009, with an initial peak value of 0.007 sr-1 until March 2010 when values have returned to background levels. Lidar measurements also show the plume descending over time. Satellite data from OMI and CALIPSO are used to track the SO2 and aerosols in the plume as it travels from the Kuril Islands to Eureka. Ground based measurements from a UV-VIS Spectrophotometer detected SO2 that correlated with OMI measurements over Eureka on July 01. A fourier transform spectrometer was used to monitor a number of chemical species in the UTLS region with HCL for example spiking during the same period. Effects of the stratospheric aerosols on the incoming short wave radiation during the summer months are also examined.

  15. Multi-wavelength Raman lidar, sunphotometric and aircraft measurements in combination with inversion models for the estimation of the aerosol optical and physico-chemical properties over Athens, Greece

    NASA Astrophysics Data System (ADS)

    Mamouri, R. E.; Papayannis, A.; Amiridis, V.; Müller, D.; Kokkalis, P.; Rapsomanikis, S.; Karageorgos, E. T.; Tsaknakis, G.; Nenes, A.; Kazadzis, S.; Remoundaki, E.

    2012-01-01

    A novel procedure has been developed to retrieve, simultaneously, the optical, microphysical and chemical properties of tropospheric aerosols with a multi-wavelength Raman lidar system in the troposphere over an urban site (Athens, Greece: 37.9° N, 23.6° E, 200 m a.s.l.) using data obtained during the European Space Agency (ESA) THERMOPOLIS project which took place between 15-31 July 2009 over the Greater Athens Area (GAA). We selected to apply our procedure for a case study of intense aerosol layers occurred on 20-21 July 2009. The National Technical University of Athens (NTUA) EOLE 6-wavelength Raman lidar system has been used to provide the vertical profiles of the optical properties of aerosols (extinction and backscatter coefficients, lidar ratio) and the water vapor mixing ratio. An inversion algorithm was used to derive the mean aerosol microphysical properties (mean effective radius - reff), single-scattering albedo (ω) and mean complex refractive index (m) at selected heights in the 2-3 km height region. We found that reff was 0.3-0.4 μm, ω at 532 nm ranged from 0.63 to 0.88 and m ranged from 1.45 + 0.015i to 1.56 + 0.05i, in good accordance with in situ aircraft measurements. The final data set of the aerosol microphysical properties along with the water vapor and temperature profiles were incorporated into the ISORROPIA model to infer an in situ aerosol composition consistent with the retrieved m and ω values. The retrieved aerosol chemical composition in the 2-3 km height region gave a variable range of sulfate (0-60%) and organic carbon (OC) content (0-50%), although the OC content increased (up to 50%) and the sulfate content dropped (up to 30%) around 3 km height; in connection with the retrieved low ω value (0.63), indicates the presence of absorbing biomass burning smoke mixed with urban haze. Finally, the retrieved aerosol microphysical properties were compared with column-integrated sunphotometer data.

  16. Property Measurement

    NASA Technical Reports Server (NTRS)

    1980-01-01

    Van is used by Land Inventory Systems to measure and map property for tax assessment purposes. It is adapted from navigation system of the Lunar Rover wheeled vehicle in which moon-exploring astronauts traveled as much as 20 miles from their Lunar Module base. Astronauts had to know their precise position so that in case of emergency they could take the shortest route back. Computerized navigational system kept a highly accurate record of the directional path providing continuous position report. Distance measuring subsystem was a more accurate counterpart of automobile odometer system counts revolutions of wheels and encoders generate electrical pulses for each fractional revolution and the computer analyzed the pulses to determine the distance traveled in a given direction.

  17. Remote Sensing of Aerosol and Cloud Properties from Ground Based and Satellite Remote Sensors to Explore Aerosol-Cloud Interaction

    NASA Astrophysics Data System (ADS)

    He, Yuzhe

    The measurements of both aerosol and cloud properties are critical for climate studies since these mechanisms have the largest uncertainty in energy balance calculations. In addition, aerosols and clouds do not act independently but can significantly couple to each other. It is clear that being able to quantify these interactions is crucial to climate models. While there are many possible aerosol-cloud interactions, we limit our investigation to the Twomey indirect effect which relates how aerosols can modify the physical properties of clouds thereby changing the radiative properties. Verifying and quantifying such mechanisms on a global scale requires accurate measurements of both aerosols and clouds from satellites. Unfortunately, assessing this mechanism has been very difficult from satellites since both aerosols and cloud properties would have to be simultaneously measured. Therefore, only statistical approaches have been tried but it is easy to see that such approaches will tend to obscure the interpretation of local interaction mechanisms. In this thesis, we investigate the potential of both satellites and ground based approaches to measure Aerosol Cloud Interaction parameters. After assessing the limitations of satellite based approaches, we focus on the use of ground based remote sensing using a combination of Lidar, Microwave radiometry, Doppler Lidar and sky radiometry. This instrumentation suite offers a more direct approach that can probe the properties of both aerosols and clouds simultaneously allowing us to investigate real time aerosol-cloud processes which occur on time scale < 1 minute. To this end, we first provide a thorough description of the multi-sensor approach and how it can be implemented including a sensitivity analysis taking into account both atmospheric and surface variability as well as uncertainty in both the Liquid Water Path (LWP) and diffuse transmittance measurements. In addition, we use the Southern Great Plain (SGP) data to

  18. Aerosols physical properties at Hada Al Sham, western Saudi Arabia

    NASA Astrophysics Data System (ADS)

    Lihavainen, H.; Alghamdi, M. A.; Hyvärinen, A.-P.; Hussein, T.; Aaltonen, V.; Abdelmaksoud, A. S.; Al-Jeelani, H.; Almazroui, M.; Almehmadi, F. M.; Al Zawad, F. M.; Hakala, J.; Khoder, M.; Neitola, K.; Petäjä, T.; Shabbaj, I. I.; Hämeri, K.

    2016-06-01

    This is the first time to clearly derive the comprehensive physical properties of aerosols at a rural background area in Saudi Arabia. Aerosol measurements station was established at a rural background area in the Western Saudi Arabia to study the aerosol properties. This study gives overview of the aerosol physical properties (PM10, PM2.5, black carbon and total number concentration) over the measurement period from November 2012 to February 2015. The average PM10 and PM2.5 concentrations were 95 ± 78 μg m-3 (mean ± STD, at ambient conditions) and 33 ± 68 μg m-3 (at ambient conditions), respectively. As expected PM10 concentration was dominated by coarse mode particles (PM10-PM2.5), most probably desert dust. Especially from February to June the coarse mode concentrations were high because of dust storm season. Aerosol mass concentrations had clear diurnal cycle. Lower values were observed around noon. This behavior is caused by wind direction and speed, during night time very calm easterly winds are dominating whereas during daytime the stronger westerly winds are dominating (sea breeze). During the day time the boundary layer is evolving, causing enhanced mixing and dilution leading to lower concentration. PM10 and PM2.5 concentrations were comparable to values measured at close by city of Jeddah. Black carbon concentration was about 2% and 6% of PM10 and PM2.5 mass, respectively. Total number concentration was dominated by frequent new particle formation and particle growth events. The typical diurnal cycle in particle total number concentration was clearly different from PM10 and PM2.5.

  19. Aerosol Properties Over the Eastern US in July 2002: Comparison of Long-Term Measurements With Results From a Coupled Meteorology-Chemistry Model

    NASA Astrophysics Data System (ADS)

    Shankar, U.; Husain, L.; Khan, A. J.; Ahmed, T.; Adelman, Z.; Xiu, A.; Arunachalam, S.

    2007-12-01

    Elemental or black carbon aerosols absorb solar radiation and have direct and indirect effect on radiative forcing. Unfortunately, global EC data are rather sparse. Therefore, for planetary radiative forcing calculations atmospheric EC burdens are obtained from model estimates based on energy consumptions. In this work we have attempted to evaluate a multiscale integrated model for aerosol physics, chemistry and radiative effects using measurements of EC and sulfate at two sites in New York State. The EC and sulfate concentrations were measured for January, February, July and August 2002 at Mayville, and Whiteface Mountain. Our Mayville site is located near Lake Chautauqua, ~ 100 km southwest of Buffalo and ~ 530 km upwind of Whiteface Mountain. Our observatory at Whiteface Mountain is located at an altitude of 1.5 km above mean sea level. Whereas at Mayville samples were collected daily, the duration of sampling at Whiteface Mountain varied from 6 to 48 h. The samples were analyzed for EC using the thermal optical method and sulfate by ion chromatography. The observations of elemental carbon and sulfate from Whiteface and Mayville for the summer of 2002 have been used along with other network measurements from the IMPROVE and CASTNet networks to evaluate METCHEM, a tightly coupled meteorology-chemistry model in nested simulations over the U.S. to examine the radiative impacts of absorbing and scattering aerosols. The model is being driven by a high-quality bottom-up inventory of emissions compiled by the Regional Planning Organizations for their 2002 visibility assessments, and the National Emissions Inventories compiled previously by the U.S. EPA in the years 2002 and 1999. The model was used to compare both the effects of evolving emissions, and the successive improvements in characterizing wildfire emissions in each of these inventories. Results of aerosol concentrations and aerosol optical depths are compared for a 3-week test period of simulation using the

  20. Aerosol Absorption in the Atmosphere: Perspectives from Global Model, Ground-Based Measurements, and Field Observations

    NASA Technical Reports Server (NTRS)

    Chin, Mian; Holben, Brent; Anderson, Tad; Quinn, Patricia; Duncan, Bryan; Ginoux, Paul

    2003-01-01

    Aerosol absorption in the atmosphere poses a major uncertainty in assessing the aerosol climate effects. This uncertainty arises from the poorly quantified aerosol sources, especially black carbon emissions, and our limited knowledge of aerosol mixing state and optical properties. Here we use a global model GOCART to simulate atmospheric aerosols, including sulfate, black carbon, organic carbon, dust, and sea salt. We compare the model calculated total aerosol optical thickness, extinction, and absorption with those quantities from the ground-based sun photometer measurements from AERONET at several different wavelengths and the field observations from ACE-Asia. We will examine what are the most sensitive factors in determining the aerosol absorption, and the consequences of assessing the aerosol radiative forcing and atmospheric heating associated with those factors.

  1. Aerosol Sources, Absorption, and Intercontinental Transport: Synergies among Models, Remote Sensing, and Atmospheric Measurements

    NASA Technical Reports Server (NTRS)

    Chin, Mian; Ginoux, Paul; Dubovik, Oleg; Holben, Brent; Kaufman, Yoram; chu, Allen; Anderson, Tad; Quinn, Patricia

    2003-01-01

    Aerosol climate forcing is one of the largest uncertainties in assessing the anthropogenic impact on the global climate system. This uncertainty arises from the poorly quantified aerosol sources, especially black carbon emissions, our limited knowledge of aerosol mixing state and optical properties, and the consequences of intercontinental transport of aerosols and their precursors. Here we use a global model GOCART to simulate atmospheric aerosols, including sulfate, black carbon, organic carbon, dust, and sea salt, from anthropogenic, biomass burning, and natural sources. We compare the model calculated aerosol extinction and absorption with those quantities from the ground-based sun photometer measurements from AERONET at several different wavelengths and the field observations from ACE-Asia, and model calculated total aerosol optical depth and fine mode fractions with the MODIS satellite retrieval. We will also estimate the intercontinental transport of pollution and dust aerosols from their source regions to other areas in different seasons.

  2. Aerosol Absorption in the Atmosphere: Perspectives from Global Model, Ground-Based Measurements, and Field Observations

    NASA Technical Reports Server (NTRS)

    Chin, Mian; Dubovik, Oleg; Holben, Brent; Torres, Omar; Anderson, Tad; Quinn, Patricia; Ginoux, Paul

    2004-01-01

    Aerosol absorption in the atmosphere poses a major uncertainty in assessing the aerosol climate effects. This uncertainty arises from the poorly quantified aerosol sources, especially black carbon emissions, and our limited knowledge of aerosol mixing state and optical properties. Here we use a global model GOCART to simulate atmospheric aerosols, including sulfate, black carbon, organic carbon, dust, and sea salt. We compare the model calculated total aerosol optical thickness, extinction, and absorption with those quantities from the ground-based sun photometer measurements from AERONET, satellite retrievals from the TOMS instrument, and field observations from ACE-Asia. We will examine the most sensitive factors in determining the aerosol absorption. and the consequences of assessing the aerosol radiative forcing and atmospheric heating associated with those factors.

  3. Aerosol Absorption in the Atmosphere: Perspectives from Global Model, Ground-Based Measurements, and Field Observations

    NASA Technical Reports Server (NTRS)

    Chin, Main; Dubovik, Oleg; Holben, Brent; Anderson, Tad; Quinn, Patricia; Duncan, Bryan; Ginoux, Paul

    2004-01-01

    Aerosol absorption in the atmosphere poses a major uncertainty in assessing the aerosol climate effects. This uncertainty arises from the poorly quantified aerosol sources, especially black carbon emissions, and our limited knowledge of aerosol mixing state and optical properties. Here we use a global model GOCART to simulate atmospheric aerosols, including sulfate, black carbon, organic carbon, dust, and sea salt. We compare the model calculated total aerosol optical thickness, extinction, and absorption with those quantities from the ground-based sun photometer measurements from AERONET at several different wavelengths and the field observations from ACE-Asia. We will examine the most sensitive factors in determining the aerosol absorption, and the consequences of assessing the aerosol radiative forcing and atmospheric heating associated with those factors.

  4. Aerosol Sources, Absorption, and Intercontinental Transport: Synergies Among Models, Remote Sensing, and Atmospheric Measurements

    NASA Technical Reports Server (NTRS)

    Chin, Mian; Chu, Allen; Levy, Robert; Remer, Lorraine; Kaufman, Yoram; Dubovik, Oleg; Holben, Brent; Eck, Tom; Anderson, Tad; Quinn, Patricia

    2004-01-01

    Aerosol climate forcing is one of the largest uncertainties in assessing the anthropogenic impact on the global climate system. This uncertainty arises from the poorly quantified aerosol sources, especially black carbon emissions, our limited knowledge of aerosol mixing state and optical properties, and the consequences of intercontinental transport of aerosols and their precursors. Here we use a global model GOCART to simulate atmospheric aerosols, including sulfate, black carbon, organic carbon, dust, and sea salt, from anthropogenic, .biomass burning, and natural sources. We compare the model calculated aerosol extinction and absorption with those quantities from the ground-based sun photometer measurements from AERON" at several different wavelengths and the field observations from ACE-Asia, and model calculated total aerosol optical depth and fine mode fractions with the MODIS satellite retrieval. We will also estimate the intercontinental transport of pollution and dust aerosols from their source regions to other areas in different seasons.

  5. Weekly periodicities of aerosol properties observed at an urban location in India

    SciTech Connect

    Satheesh, S K; Vinoj, V; Moorthy, K Krishna

    2011-07-01

    Multi-year (~7 years) observations of aerosol optical and microphysical properties were conducted at a tropical urban location in Bangalore, India. As a consequence of rapid urbanization, Bangalore presents high local atmospheric emissions, which makes it an interesting site to study the effect of anthropogenic activities on aerosol properties. It has been found that both column (aerosol optical depth, AOD) and ground-level measurements (black carbon (BC) and composite aerosol mass) exhibit a weekly cycle with low aerosol concentrations on weekends. In comparison to the weekdays, the weekend reductions of aerosol optical depth, black carbon and composite aerosol mass concentrations were ~15%, 25% and 24%, respectively. The magnitude of weekend reduction of black carbon is as much as ~1 μg m-3. The similarity in the weekly cycle between the column and surface measurements suggests that the aerosol column loading at this location is governed by local anthropogenic emissions. The strongest weekly cycle in composite aerosol mass concentration was observed in the super micron mass range (>1 μm). The weekly cycle of composite aerosol mass in the sub micron mass range (<1 μm) was weak in comparison to the super micron aerosol mass.

  6. Atmospheric Radiation Measurements Aerosol Intensive Operating Period: Comparison of Aerosol Scattering during Coordinated Flights

    NASA Technical Reports Server (NTRS)

    Hallar, A. G.; Strawa, A. W.; Schmid, B.; Andrews, E.; Ogren, J.; Sheridan, P.; Ferrare, R.; Covert, D.; Elleman, R.; Jonsson, H.; Bokarius, K.; Luu, A.

    2006-01-01

    In May 2003, a Twin Otter airplane, equipped with instruments for making in situ measurements of aerosol optical properties, was deployed during the Atmospheric Radiation Measurements (ARM) Program s Aerosol Intensive Operational Period in Oklahoma. Several of the Twin Otter flights were flown in formation with an instrumented light aircraft (Cessna 172XP) that makes routine in situ aerosol profile flights over the site. This paper presents comparisons of measured scattering coefficients at 467 nm, 530 nm, and 675 nm between identical commercial nephelometers aboard each aircraft. Overall, the agreement between the two nephelometers decreases with longer wavelength. During the majority of the flights, the Twin Otter flew with a diffuser inlet while the Cessna had a 1 mm impactor, allowing for an estimation of the fine mode fraction aloft. The fine mode fraction aloft was then compared to the results of a ground-based nephelometer. Comparisons are also provided in which both nephelometers operated with identical 1 mm impactors. These scattering coefficient comparisons are favorable at the longer wavelengths (i.e., 530 nm and 675 nm), yet differed by approximately 30% at 467 nm. Mie scattering calculations were performed using size distribution measurements, made during the level flight legs. Results are also presented from Cadenza, a new continuous wave cavity ring-down (CW-CRD) instrument, which compared favorably (i.e., agreed within 2%) with data from other instruments aboard the Twin Otter. With this paper, we highlight the significant implications of coarse mode (larger than 1 mm) aerosol aloft with respect to aerosol optical properties.

  7. Background Southeast United States Aerosol Optical Properties and Their Dependence Upon Meteorology

    NASA Astrophysics Data System (ADS)

    Pawlyszyn, C.; West, M.; Sherman, J. P.; Link, M.; Zhou, Y.

    2015-12-01

    Aerosol effects on SE U.S. radiation budget are highly-seasonal. Aerosol loading is much higher in summer, due largely to high levels of biogenic secondary organic aerosol and sulfates. Aerosol loading is lowest in winter. Aerosol optical properties relevant to radiative forcing have been measured continuously at the Appalachian Atmospheric Interdisciplinary Research facility (AppalAIR) since the summer of 2009. AppalAIR is the only site in the eastern US to house co-located NOAA ESRL and NASA AeroNET instrumentation and is located in the mountains of Boone, NC. Lower tropospheric sub-micron (PM1) light scattering and absorption coefficients measured over seven summers and six winters are presented here, in addition to PM1 organic and sulfate aerosol mass concentrations measured during summers 2012-2013 as well as winter 2013. The objective is to determine the influence of aerosol sources and meteorology along the air mass back-trajectories on aerosol loading and composition. PM1 aerosol mass was dominated by organic aerosol and sulfate during the periods measured. Aerosol light scattering and organic aerosol concentrations were positively correlated during summer with temperature and solar flux along the parcel back-trajectory and negatively-correlated with rainfall along the back-trajectory. Wet deposition was a major factor in the difference between the upper and lower scattering coefficient quartiles for both summer and winter. Summer PM1 light scattering coefficient declined by approximately 30-40% since 2009, with smaller decreases during winter months. Long-term studies of aerosol optical properties from the regionally-representative AppalAIR site are necessary to determine the relationships between changing SE U.S. air quality and aerosol effects on regional climate and weather.

  8. Optical properties of aerosols over the eastern Mediterranean

    NASA Astrophysics Data System (ADS)

    Bryant, C.; Eleftheriadis, K.; Smolik, J.; Zdimal, V.; Mihalopoulos, N.; Colbeck, I.

    Measurements of aerosol optical properties, size distribution and chemical composition were conducted at Finokalia, a remote coastal site on the Greek island of Crete (35°19'N, 25°40'E) during July 2000 and January 2001. During the summer campaign the total scattering coefficient, σ, (at a wavelength of 550 nm) ranged from 13 to 120 Mm -1 (mean=44.2 Mm -1, standard deviation=17.5) whilst during the winter it ranged from 7.22 to 37.8 Mm -1 (mean=18.42 Mm -1, standard deviation=6.61). A distinct diurnal variation in scattering coefficients was observed, with minima occurring during the early morning and maxima in the late afternoon during the summer and late evening during the winter. The mean value of the Ångström exponent was 1.47 during the summer and 1.28 during the winter, suggesting a larger fraction of smaller particles at the site during the summer. This was confirmed by continuous measurements of the aerosol size distribution. An analysis of the single scattering albedo suggests that there is a more absorbing fraction in the particle composition in the summer than during the winter. An investigation of air mass origins on aerosol optical properties indicated that those from Turkey and Central/Eastern Europe were highly polluted with a corresponding impact on aerosol optical properties. A linear relationship was obtained between the total scattering coefficient and both the non-sea-salt sulphate concentrations and the fine aerosol fraction.

  9. A New Stratospheric Aerosol Product from CALIPSO Lidar Measurements

    NASA Astrophysics Data System (ADS)

    Kar, J.; Vaughan, M.; Trepte, C. R.; Winker, D. M.; Vernier, J. P.; Pitts, M. C.; Young, S. A.; Liu, Z.; Lucker, P.; Tackett, J. L.; Omar, A. H.

    2014-12-01

    Stratospheric aerosols are derived from precursor SO2 and OCS gases transported from the lower troposphere. Volcanic injections can also enhance aerosol loadings far above background levels. The latter can exert a significant influence on the Earth's radiation budget for major and even minor eruptions. Careful measurements are needed, therefore, to monitor the distribution and evolution of stratospheric aerosols for climate related studies. The Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observations (CALIPSO) mission has been acquiring profile measurements of clouds and aerosols since 2006, leading to major advances in our understanding of tropospheric aerosol and cloud properties and the processes that control them. The CALIPSO products have also enabled new insights into polar stratospheric clouds and stratospheric aerosols. Vernier et al (2009,JGR,114,D00H10) reported on the construction of a modified CALIPSO lidar product that corrected minor artifacts with the original lidar calibration that affected stratospheric aerosol investigations. A significantly improved CALIPSO Lidar Version 4 Level 1 product has been recently released addressing these calibration issues and has resulted in enhanced signal levels and a highly stable record over the span of the mission. Based on this product, a new 3D gridded stratospheric CALIPSO data product is under development and being targeted for release in 2015. A key emphasis of this new product is to bridge the measurement gap between the SAGE II and SAGE III data record (1984-2005) and the start of measurements from the new SAGE III instrument to be deployed on the International Space Station in 2016. The primary parameters delivered in the CALIPSO stratospheric data products will be attenuated scattering ratio and aerosol extinction profiles, both averaged over one month intervals and binned into an equal angle grid of constant latitude and longitude with a vertical resolution of 900m. We will present the overall

  10. Organic Aerosol Composition Measurements at the DOE Atmospheric Radiation Measurement Sites

    NASA Astrophysics Data System (ADS)

    Parworth, C. L.; Zhang, Q.; Fast, J. D.; Shippert, T.; Sivaraman, C.; Mei, F.; Tilp, A.

    2012-12-01

    Organic aerosol (OA) makes up a large portion of aerosols in the atmosphere. A better understanding of the chemical composition of OA is needed to quantify the effects that aerosols have on radiation and clouds. OA is composed of thousands of species making its chemical and physical properties difficult to characterize. The complex composition of OA can be decomposed into several factors representative of distinct sources and evolution processes through the application of Positive Matrix Factorization (PMF) on ambient OA data acquired with aerosol mass spectrometers (AMS). Previous studies have shown that the OA factors thus determined can be particularly useful for closure studies on aerosol optical and cloud condensation properties. Three units of Aerosol Chemical Speciation Monitor (ACSM) were recently added to two long-term measurement sites (Tropical Western Pacific and Southern Great Plains) and a mobile facility supported by the DOE ARM program. An ACSM is a smaller version of an AMS that provides long term, continuous measurements of aerosols and requires low maintenance. In this presentation, we will report the development of methods that take measurements of total organic matter and mass spectral information from the ACSM and derive OA factors. We will describe how the OA factors are derived, the quality assurance (QA) procedures, and comparisons of side-by-side measurements from AMS and ACSM instruments. The code generated in this analysis will be run within the Data Management Facility of ARM and the new data product called the Organic Aerosol Composition (Oacomp) value-added product will be added to the ARM archive. We will also present data from over a year-long period from the SGP site, along with an analysis that explains the seasonal and multi-day variations in inorganic and organic aerosol components.

  11. Comparison of Aerosol Properties Within and Above the ABL at the ARM Program's SGP Site

    SciTech Connect

    Delle Monache, L

    2002-05-01

    The goal of this thesis is to determine under what conditions, if any, measurements of aerosol properties made at the Earth's surface are representative of aerosol properties within the column of air above the surface. This thesis will use data from the Atmospheric Radiation Measurement (ARM) site at the Southern Great Plains (SGP) which is the only location in the world where ground-based and in situ airborne measurements are made on a routine basis. All flight legs in the one-year period from March 2000-March 2001 were categorized as either within or above the atmospheric boundary layer using an objective mixing height determination technique. The correlations between the aerosol properties measured at the surface and the measured within and above the ABL were then computed. The conclusion of this comparison is that the aerosol extensive and intensive properties measured at the surface are representative of values within the ABL, but not within the free atmosphere.

  12. A comprehensive climatology of Arctic aerosol properties on the North Slope of Alaska

    NASA Astrophysics Data System (ADS)

    Creamean, Jessie; de Boer, Gijs; Shupe, Matthew; McComiskey, Allison

    2016-04-01

    Evaluating aerosol properties has implications for the formation of Arctic clouds, resulting in impacts on cloud lifetime, precipitation processes, and radiative forcing. There are many remaining uncertainties and large discrepancies regarding modeled and observed Arctic aerosol properties, illustrating the need for more detailed observations to improve simulations of Arctic aerosol and more generally, projections of the components of the aerosol-driven processes that impact sea ice loss/gain. In particular, the sources and climatic effects of Arctic aerosol particles are severely understudied. Here, we present a comprehensive, long-term record of aerosol observations from the North Slope of Alaska baseline site at Barrow. These measurements include sub- and supermicron (up to 10 μm) total mass and number concentrations, sub- and supermicron soluble inorganic and organic ion concentrations, submicron metal concentrations, submicron particle size distributions, and sub- and supermicron absorption and scattering properties. Aerosol extinction and number concentration measurements extend back to 1976, while the remaining measurements were implemented since. Corroboration between the chemical, physical, and optical property measurements is evident during periods of overlapping observations, demonstrating the reliability of the measurements. During the Arctic Haze in the winter/spring, high concentrations of long-range transported submicron sea salt, mineral dust, industrial metals, pollution (non-sea salt sulfate, nitrate, ammonium), and biomass burning species are observed concurrent with higher concentrations of particles with sizes that span the submicron range, enhanced absorption and scattering coefficients, and largest Ångström exponents. The summer is characterized by high concentrations of small biogenic aerosols (< 100 nm) and low extinction coefficients. Fall is characterized by clean conditions, with supermicron sea salt representing the dominant aerosol

  13. Chamber LIDAR measurements of aerosolized biological simulants

    NASA Astrophysics Data System (ADS)

    Brown, David M.; Thrush, Evan P.; Thomas, Michael E.; Siegrist, Karen M.; Baldwin, Kevin; Quizon, Jason; Carter, Christopher C.

    2009-05-01

    A chamber aerosol LIDAR is being developed to perform well-controlled tests of optical scattering characteristics of biological aerosols, including Bacillus atrophaeus (BG) and Bacillus thuringiensis (BT), for validation of optical scattering models. The 1.064 μm, sub-nanosecond pulse LIDAR allows sub-meter measurement resolution of particle depolarization ratio or backscattering cross-section at a 1 kHz repetition rate. Automated data acquisition provides the capability for real-time analysis or recording. Tests administered within the refereed 1 cubic meter chamber can provide high quality near-field backscatter measurements devoid of interference from entrance and exit window reflections. Initial chamber measurements of BG depolarization ratio are presented.

  14. Aerosol measurements at the South Pole

    NASA Astrophysics Data System (ADS)

    Bodhaine, Barry A.; Deluisi, John J.; Harris, Joyce M.; Houmere, Pamela; Bauman, Sene

    1986-09-01

    Some results are given regarding the aerosol measurement program conducted by the NOAA at their atmospheric monitoring observatory at Amundsen-Scott Station, South Pole. The program consists of the continuous measurement of condensation nuclei (CN) concentration and aerosol scattering extinction coefficient. A time series of sodium, chlorine, and sulfur concentrations shows that the sulfur and CN records are similar and that the sodium, chlorine, and extinction coefficient records are similar. Large episodes of sodium are measured at the ground in the austral winter and are apparently caused by large-scale warming and weakening of the surface temperature inversion. The CN data show an annual cycle with a maximum exceeding 100 per cubic centimeter in the austral summer and a minimum of about 10 per cubic centimeter in the winter. The extinction coefficient data show an anual cycle markedly different from that of CN with a maximum in late winter, a secondary maximum in summer, and a minimum in May.

  15. Characterization of a Photoacoustic Aerosol Absorption Spectrometer for Aircraft-based Measurements

    NASA Astrophysics Data System (ADS)

    Mason, B. J.; Wagner, N. L.; Richardson, M.; Brock, C. A.; Murphy, D. M.; Adler, G.

    2015-12-01

    Atmospheric aerosol directly impacts the Earth's climate through extinction of incoming and outgoing radiation. The optical extinction is due to both scattering and absorption. In situ measurements of aerosol extinction and scattering are well established and have uncertainties less than 5%. However measurements of aerosol absorption typically have uncertainties of 20-30%. Development and characterization of more accurate and precise instrumentation for measurement of aerosol absorption will enable a deeper understand of significance and spatial distribution of black and brown carbon aerosol, the effect of atmospheric processes on aerosol optical properties, and influence of aerosol optical properties on direct radiative forcing. Here, we present a detailed characterization of a photoacoustic aerosol absorption spectrometer designed for deployment aboard research aircraft. The spectrometer operates at three colors across the visible spectrum and is calibrated in the field using ozone. The field calibration is validated in the laboratory using synthetic aerosol and simultaneous measurements of extinction and scattering. In addition, the sensitivity of the instrument is characterized under conditions typically encountered during aircraft sampling e.g. as a function of changing pressure. We will apply this instrument characterization to ambient aerosol absorption data collected during the SENEX and SEAC4RS aircraft based field campaigns.

  16. Aerosol optical properties and radiative effects in the Yangtze Delta region of China

    NASA Astrophysics Data System (ADS)

    Xia, Xiangao; Li, Zhanqing; Holben, Brent; Wang, Pucai; Eck, Tom; Chen, Hongbin; Cribb, Maureen; Zhao, Yanxia

    2007-11-01

    One year's worth of aerosol and surface irradiance data from September 2005 to August 2006 were obtained at Taihu, the second supersite for the East Asian Study of Tropospheric Aerosols: An International Regional Experiment (EAST-AIRE). Aerosol optical properties derived from measurements by a Sun photometer were analyzed. The aerosol data were used together with surface irradiance data to quantitatively estimate aerosol effects on surface shortwave radiation (SWR) and photosynthetically active radiation (PAR). The annual mean aerosol optical depth at 500 nm is 0.77, and mean Ångstrom wavelength exponent is 1.17. The annual mean aerosol single scattering albedo and mean aerosol asymmetry factor at 440 nm are 0.90 and 0.72, respectively. Both parameters show a weak seasonal variation, with small values occurring during the winter and larger values during the summer. Clear positive relationships between relative humidity and aerosol properties suggest aerosol hygroscopic growth greatly modifies aerosol properties. The annual mean aerosol direct radiative forcing at the surface (ADRF) is -38.4 W m-2 and -17.8 W m-2 for SWR and PAR, respectively. Because of moderate absorption, the instantaneous ADRF at the top of the atmosphere derived from CERES SSF data is close to zero. Heavy aerosol loading in this region leads to -112.6 W m-2 and -45.5 W m-2 reduction in direct and global SWR, but 67.1 W m-2 more diffuse SWR reaching the surface. With regard to PAR, the annual mean differences in global, direct and diffuse irradiance are -23.1 W m-2, -65.2 W m-2 and 42.1 W m-2 with and without the presence of aerosol, respectively.

  17. Aerosol Characterization and New Instrumentation for Better Understanding Snow Radiative Properties

    NASA Astrophysics Data System (ADS)

    Beres, N. D.

    2015-12-01

    Snow albedo is determined by snowpack thickness and grain size, but also affected by contamination with light-absorbing, microscopic (e.g., mineral dust, combustion aerosols, bio-aerosols) and macroscopic (e.g., microalgae, plant debris, sand, organisms) compounds. Most currently available instruments for measuring snow albedo utilize the natural, downward flux of solar radiation and the reflected upward flux. This reliance on solar radiation (and, thus, large zenith angles and clear-sky conditions) leads to severe constraints, preventing characterization of detailed diurnal snow albedo cycles. Here, we describe instrumentation and methodologies to address these limitations with the development and deployment of new snow radiation sensors for measuring surface spectral and in-snow radiative properties. This novel instrumentation will be tested at the CRREL/UCSB Eastern Sierra (CUES) Snow Study Site at Mammoth Mountain, which is extensively instrumented for characterizing snow properties including snow albedo and surface morphology. However, it has been lacking instrumentation for the characterization of aerosols that can be deposited on the snow surface through dry and wet deposition. Currently, we are installing aerosol instrumentation at the CUES site, which are also described. This includes instruments for the multi-wavelength measurement of aerosol scattering and absorption coefficients and for the characterization of aerosol size distribution. Knowledge of aerosol concentration and physical and optical properties will allow for the study of aerosol deposition and modification of snow albedo and for establishing an aerosol climatology for the CUES site.

  18. Comparison of Aerosol Properties within and above the ABL at the ARM Program's SGP Site

    SciTech Connect

    Monache, L.D.; Perry, K.D.; Cederwall, R.T.

    2002-02-26

    The goal of this study was to determine under what conditions, if any, measurements of aerosol properties made at the Earth's surface are representative of the aerosol properties within the column of air above the surface. This project used data from the Atmospheric Radiation Measurement (ARM) site at the Southern Great Plains (SGP) site (Stokes and Schwartz 1994), which is one of the only locations in the world where ground-based and in situ airborne measurements of atmospheric aerosol are made on a routine basis. All flight legs in the one-year period from March 2000 to March 2001 were categorized as either within or above the atmospheric boundary layer (ABL) using an objective mixing height determination technique. The correlations between the aerosol properties measured at the surface and those measured within and above the ABL were then computed. The conclusion of this comparison is that the aerosol extensive properties (those that depend upon the amount of aerosol that is present in the atmosphere, i.e., either the number or mass concentrations), and intensive properties (those that do not depend upon the amount of aerosol present) measured at the surface are representative of values within the ABL, but not within the free atmosphere.

  19. Multi-wavelength Raman lidar, sun photometric and aircraft measurements in combination with inversion models for the estimation of the aerosol optical and physico-chemical properties over Athens, Greece

    NASA Astrophysics Data System (ADS)

    Mamouri, R. E.; Papayannis, A.; Amiridis, V.; Müller, D.; Kokkalis, P.; Rapsomanikis, S.; Karageorgos, E. T.; Tsaknakis, G.; Nenes, A.; Kazadzis, S.; Remoundaki, E.

    2012-07-01

    A novel procedure has been developed to retrieve, simultaneously, the optical, microphysical and chemical properties of tropospheric aerosols with a multi-wavelength Raman lidar system in the troposphere over an urban site (Athens, Greece: 37.9° N, 23.6° E, 200 m a.s.l.) using data obtained during the European Space Agency (ESA) THERMOPOLIS project, which took place between 15-31 July 2009 over the Greater Athens Area (GAA). We selected to apply our procedure for a case study of intense aerosol layers that occurred on 20-21 July 2009. The National Technical University of Athens (NTUA) EOLE 6-wavelength Raman lidar system has been used to provide the vertical profiles of the optical properties of aerosols (extinction and backscatter coefficients, lidar ratio) and the water vapor mixing ratio. An inversion algorithm was used to derive the mean aerosol microphysical properties (mean effective radius (reff), single-scattering albedo ω) and mean complex refractive index (m)) at selected heights in the 2-3 km height region. We found that reff was 0.14-0.4 (±0.14) μm, ω was 0.63-0.88 (±0.08) (at 532 nm) and m ranged from 1.44 (±0.10) + 0.01 (±0.01)i to 1.55 (±0.12) + 0.06 (±0.02)i, in good agreement (only for the reff values) with in situ aircraft measurements. The water vapor and temperature profiles were incorporated into the ISORROPIA II model to propose a possible in situ aerosol composition consistent with the retrieved m and ω values. The retrieved aerosol chemical composition in the 2-3 km height region gave a variable range of sulfate (0-60%) and organic carbon (OC) content (0-50%), although the OC content increased (up to 50%) and the sulfate content dropped (up to 30%) around 3 km height; the retrieved low ω value (0.63), indicates the presence of absorbing biomass burning smoke mixed with urban haze. Finally, the retrieved aerosol microphysical properties were compared with column-integrated sun photometer CIMEL data.

  20. Star Photometry for the Characterization of Columnar Aerosol Properties

    NASA Astrophysics Data System (ADS)

    Perez-Ramirez, D.; Lyamani, H.; Olmo Reyes, F. J.; Alados-Arboledas, L.; Whiteman, D. N.; Aceituno, J.

    2015-12-01

    Knowledge of columnar aerosol particles at nighttime is essential to completely understand aerosol dynamics and so will largely improve aerosol models. However, the current knowledge columnar nighttime aerosol is poor due to the lack of continuous measurements partly associated with previous technological limitations. Here we present the development, set up, calibration and data quality algorithms for the star photometer at the station of Granada (37.16 N, 3.60 W, 680 m a.s.l.) in Spain. The main advantage of this instrument is that make uses of a CCD camera as detector allowing direct star flux measurements. Filters center at 380, 440, 500, 670, 880 and 1020 nm allows spectral aerosol optical depth (AOD) measurements. Among all the stars, only those that are isolated and possess constant extratarrestial flux are considered. Two methods for the calibration of the system at high mountain places are presented. The first one consists of doing a Langley calibration of a selected star together with measurements of other stars. From the Langley calibration, we transferred AOD and get the calibration constants for other stars. The second method is the Astronomical Langley Method that consists of dividing the measurements by the optical air mass and so more stable calibration constant are obtained. On the other hand, the atmospheric turbulence is important for very short exposure times (< 1 s) and so uncertainties in AOD are of ±0.02 for λ < 800nm and ±0.01 for λ > 800nm. The instrument operated continuously for more than four consecutive years and so a large database was created. Cloud screening and data quality algorithms following AERONET inheritance were developed. Basically, moving averages are applied with different temporal-windows combined with a procedure to detect outliers. On the other hand, with quality data guaranteed the analysis of day-to-night columnar aerosol properties is presented. Mean AOD(440 nm) (0.18 ± 0.10 and 0.19 ± 0.11 for daytime and

  1. Aerosol properties, source identification, and cloud processing in orographic clouds measured by single particle mass spectrometry on a Central European mountain site during HCCT-2010

    NASA Astrophysics Data System (ADS)

    Roth, A.; Schneider, J.; Klimach, T.; Mertes, S.; van Pinxteren, D.; Herrmann, H.; Borrmann, S.

    2015-09-01

    Cloud residues and out-of-cloud aerosol particles with diameters between 150 and 900 nm have been analysed by on-line single particle aerosol mass spectrometry during the six-week study HCCT-2010 in September/October 2010. The measurement location was the mountain Schmücke (937 m a.s.l.) in Central Germany. More than 170 000 bipolar mass spectra from out-of-cloud aerosol particles and more than 14 000 bipolar mass spectra from cloud residual particles were obtained and were classified using a fuzzy c-means clustering algorithm. Analysis of the uncertainty of the sorting algorithm was conducted on a subset of the data by comparing the clustering output with particle-by-particle inspection and classification by the operator. This analysis yielded a false classification probability between 13 and 48 %. Additionally, particle types were identified by specific marker ions. The results from the ambient aerosol analysis show that 63 % of the analysed particles belong to clusters indicating a diurnal variation, suggesting that local or regional sources dominate the aerosol, especially for particles containing soot and biomass burning particles. In the cloud residues the relative percentage of large soot-containing particles and particles containing amines was found to be increased compared to the out-of-cloud aerosol, while in general organic particles were less abundant in the cloud residues. In the case of amines this can be explained by the high solubility of the amines, while the large soot-containing particles were found to be internally mixed with inorganics, which explains their activation as cloud condensation nuclei. Furthermore, the results show that during cloud processing, both sulphate and nitrate are added to the residual particles, thereby changing the mixing state and increasing the fraction of particles with nitrate and/or sulphate. This is expected to lead to higher hygroscopicity after cloud evaporation, and therefore to an increase of the particles

  2. Aerosol properties, source identification, and cloud processing in orographic clouds measured by single particle mass spectrometry on a central European mountain site during HCCT-2010

    NASA Astrophysics Data System (ADS)

    Roth, A.; Schneider, J.; Klimach, T.; Mertes, S.; van Pinxteren, D.; Herrmann, H.; Borrmann, S.

    2016-01-01

    Cloud residues and out-of-cloud aerosol particles with diameters between 150 and 900 nm were analysed by online single particle aerosol mass spectrometry during the 6-week study Hill Cap Cloud Thuringia (HCCT)-2010 in September-October 2010. The measurement location was the mountain Schmücke (937 m a.s.l.) in central Germany. More than 160 000 bipolar mass spectra from out-of-cloud aerosol particles and more than 13 000 bipolar mass spectra from cloud residual particles were obtained and were classified using a fuzzy c-means clustering algorithm. Analysis of the uncertainty of the sorting algorithm was conducted on a subset of the data by comparing the clustering output with particle-by-particle inspection and classification by the operator. This analysis yielded a false classification probability between 13 and 48 %. Additionally, particle types were identified by specific marker ions. The results from the ambient aerosol analysis show that 63 % of the analysed particles belong to clusters having a diurnal variation, suggesting that local or regional sources dominate the aerosol, especially for particles containing soot and biomass burning particles. In the cloud residues, the relative percentage of large soot-containing particles and particles containing amines was found to be increased compared to the out-of-cloud aerosol, while, in general, organic particles were less abundant in the cloud residues. In the case of amines, this can be explained by the high solubility of the amines, while the large soot-containing particles were found to be internally mixed with inorganics, which explains their activation as cloud condensation nuclei. Furthermore, the results show that during cloud processing, both sulfate and nitrate are added to the residual particles, thereby changing the mixing state and increasing the fraction of particles with nitrate and/or sulfate. This is expected to lead to higher hygroscopicity after cloud evaporation, and therefore to an increase of

  3. Cloud droplet nucleation and its connection to aerosol properties

    SciTech Connect

    Schwartz, S.E.

    1996-04-01

    Anthropogenic aerosols influence the earth`s radiation balance and climate directly, by scattering shortwave (solar) radiation in cloud-free conditions and indirectly, by increasing concentrations of cloud droplets thereby enhancing cloud shortwave reflectivity. These effects are thought to be significant in the context of changes in the earth radiation budget over the industrial period, exerting a radiative forcing that is of comparable magnitude to that of increased concentrations of greenhouse gases over this period but opposite in sign. However the magnitudes of both the direct and indirect aerosol effects are quite uncertain. Much of the uncertainty of the indirect effect arises from incomplete ability to describe changes in cloud properties arising from anthropogenic aerosols. This paper examines recent studies pertaining to the influence of anthropogenic aerosols on loading and properties of aerosols affecting their cloud nucleating properties and indicative of substantial anthropogenic influence on aerosol and cloud properties over the North Atlantic.

  4. Aerosol Optical Properties During The SAMUM-2 Experiment

    NASA Astrophysics Data System (ADS)

    Toledano, C.; Freudenthaler, V.; Gross, S.; Seefeldner, M.; Gasteiger, J.; Garhammer, M.; Esselborn, M.; Wiegner, M.; Koepke, P.

    2009-03-01

    A field campaign of the Saharan Mineral Dust Experiment (SAMUM-2) took place in the Cape Verde islands in January-February 2008, to investigate the properties of long-range transported dust over the Atlantic. The Meteorological Institute of the University of Munich deployed a set of active and passive remote sensing instruments: one sun photometer, for the measurement of the direct sun irradiance and sky radiances; a broad-band UV radiometer; and 2 tropospheric lidar systems. The measurements were made in close cooperation with the other participating groups. During the measurement period the aerosol scenario over Cape Verde mostly consisted of a dust layer below 2 km and a smoke layer above 2 km height. The Saharan dust arrived in the site from the NE, whereas the smoke originated in the African equatorial region is transported from the SE. The aerosol load was also very variable over this area, with AOD (500 nm) ranging from 0.04 to 0.74. The optical properties of the layers are shown: extinction and particle depolarization ratio profiles at 3 wavelengths, as well as aerosol optical depth (in the range 340-1550 nm), Ångström exponent, size distribution and single scattering albedo.

  5. Aerosol measurements in the IR: from limb to nadir?

    NASA Technical Reports Server (NTRS)

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

    2001-01-01

    Vertical profiles of aerosol concentration have been derived from the ATMOS solar occultation dataset. The EOS instrument TES has motivated studies of the feasibility of quantifying aerosols in nadir and limb emission measurements.

  6. Radiative Properties of Smoke and Aerosol Over Land Surfaces

    NASA Technical Reports Server (NTRS)

    King, Michael D.

    2000-01-01

    This talk discusses smoke and aerosol's radiative properties with particular attention to distinguishing the measurement over clear sky from clouds over land, sea, snow, etc. surfaces, using MODIS Airborne Simulator data from (Brazil, arctic sea ice and tundra and southern Africa, west Africa, and other ecosystems. This talk also discusses the surface bidirectional reflectance using Cloud Absorption Radiometer, BRDF measurements of Saudi Arabian desert, Persian Gulf, cerrado and rain forests in Brazil, sea ice, tundra, Atlantic Ocean, Great Dismal Swamp, Kuwait oil fire smoke. Recent upgrades to instrument (new TOMS UVA channels at 340 and 380 planned use in Africa (SAFARI 2000) and possibly for MEIDEX will also be discussed. This talk also plans to discuss the spectral variation of surface reflectance over land and the sensitivity of off-nadir view angles to correlation between visible near-infrared reflectance for use in remote sensing of aerosol over land.

  7. Aerosol optical properties in the Marine Environment during the TCAP-I campaign

    NASA Astrophysics Data System (ADS)

    Chand, D.; Berg, L. K.; Barnard, J.; Berkowitz, C. M.; Burton, S. P.; Chapman, E. G.; Comstock, J. M.; Fast, J. D.; Ferrare, R. A.; Connor, F. J.; Hair, J. W.; Hostetler, C. A.; Hubbe, J.; Kluzek, C.; Mei, F.; Pekour, M. S.; Sedlacek, A. J.; Schmid, B.; Shilling, J. E.; Shinozuka, Y.; Tomlinson, J. M.; Wilson, J. M.; Zelenyuk-Imre, A.

    2013-12-01

    The role of direct radiative forcing by atmospheric aerosol is one of the largest sources of uncertainty in predicting climate change. Much of this uncertainty comes from the limited knowledge of observed aerosol optical properties. In this presentation we discuss derived aerosol optical properties based on measurements made during the summer 2012 Two-Column Aerosol Project-I (TCAP) campaign and relate these properties to the corresponding chemical and physical properties of the aerosol. TCAP was designed to provide simultaneous, in-situ observations of the size distribution, chemical properties, and optical properties of aerosol within and between two atmospheric columns over the Atlantic Ocean near the eastern seaboard of the United States. These columns are separated by 200-300 km and were sampled in July 2012 during a summer intensive operation period (IOP) using the U.S. Department of Energy's Gulfstream-1 (G-1) and NASA's B200 aircraft, winter IOP using G-1 aircraft in February 2013, and the surface-based DOE Atmospheric Radiation Measurement (ARM) Mobile Facility (AMF) located on Cape Cod. In this presentation we examine the spectral dependence of the aerosol optical properties measured from the aircraft over the TCAP-I domain, with an emphasis on in-situ derived intensive properties measured by a 3-λ Nephelometer, a Particle Soot Absorption Photometer (PSAP), a humidograph (f(RH)), and a Single Particle Soot Photometer (SP2). Preliminary results indicate that the aerosol are more light-absorbing as well as more hygroscopic at higher altitudes (2-4 km) compared to the corresponding values made within residual layers near the surface (0-2 km altitude). The average column (0-4 km) single scattering albedo (ω) and hygroscopic scattering factor (F) are found to be ~0.96 and 1.25, respectively. Additional results on key aerosol intensive properties such as the angstrom exponent (å), asymmetry parameter (g), backscattering fraction (b), and gamma parameter (

  8. Size distribution and scattering phase function of aerosol particles retrieved from sky brightness measurements

    NASA Technical Reports Server (NTRS)

    Kaufman, Y. J.; Gitelson, A.; Karnieli, A.; Ganor, E. (Editor); Fraser, R. S.; Nakajima, T.; Mattoo, S.; Holben, B. N.

    1994-01-01

    Ground-based measurements of the solar transmission and sky radiance in a horizontal plane through the Sun are taken in several geographical regions and aerosol types: dust in a desert transition zone in Israel, sulfate particles in Eastern and Western Europe, tropical aerosol in Brazil, and mixed continental/maritime aerosol in California. Stratospheric aerosol was introduced after the eruption of Mount Pinatubo in June 1991. Therefore measurements taken before the eruption are used to analyze the properties of tropospheric aerosol; measurements from 1992 are also used to detect the particle size and concentration of stratospheric aerosol. The measurements are used to retrieve the size distribution and the scattering phase function at large scattering angles of the undisturbed aerosol particles. The retrieved properties represent an average on the entire atmospheric column. A comparison between the retrieved phase function for a scattering angle of 120 deg, with phase function predicted from the retrieved size distribution, is used to test the assumption of particle homogeneity and sphericity in radiative transfer models (Mie theory). The effect was found to be small (20% +/- 15%). For the stratospheric aerosol (sulfates), as expected, the phase function was very well predicted using the Mie theory. A model with a power law distribution, based on the spectral dependence of the optical thickness, alpha, cannot estimate accurately the phase function (up to 50% error for lambda = 0.87 microns). Before the Pinatubo eruption the ratio between the volumes of sulfate and coarse particles was very well correlated with alpha. The Pinatubo stratospheric aerosol destroyed this correlation. The aerosol optical properties are compared with analysis of the size, shape, and composition of the individual particles by electron microscopy of in situ samples. The measured volume size distribution before the injection of stratospheric aerosol consistently show two modes, sulfate

  9. Columnar aerosol optical properties at AERONET sites in central eastern Asia and aerosol transport to the tropical mid-Pacific

    NASA Astrophysics Data System (ADS)

    Eck, T. F.; Holben, B. N.; Dubovik, O.; Smirnov, A.; Goloub, P.; Chen, H. B.; Chatenet, B.; Gomes, L.; Zhang, X.-Y.; Tsay, S.-C.; Ji, Q.; Giles, D.; Slutsker, I.

    2005-03-01

    The column-integrated optical properties of aerosol in the central eastern region of Asia and midtropical Pacific were investigated based on Sun/sky radiometer measurements made at Aerosol Robotic Network (AERONET) sites in these regions. Characterization of aerosol properties in the Asian region is important due to the rapid growth of both population and economic activity, with associated increases in fossil fuel combustion, and the possible regional and global climatic impacts of related aerosol emissions. Multiyear monitoring over the complete annual cycle at sites in China, Mongolia, South Korea, and Japan suggest spring and/or summer maximum in aerosol optical depth (τa) and a winter minimum; however, more monitoring is needed to establish accurate climatologies. The annual cycle of Angstrom wavelength exponent (α) showed a springtime minimum associated with dust storm activity; however, the monthly mean α440-870 was >0.8 even for the peak dust season at eastern Asian sites suggesting that fine mode pollution aerosol emitted from population centers in eastern Asia dominates the monthly aerosol optical influence even in spring as pollution aerosol mixes with coarse mode dust originating in western source regions. Aerosol optical depth peaks in spring in the tropical mid-Pacific Ocean associated with seasonal shifts in atmospheric transport from Asia, and ˜35% of the springtime τa500 enhancement occurs at altitudes above 3.4 km. For predominately fine mode aerosol pollution cases, the average midvisible (˜550 nm) single scattering albedo (ω0) at two continental urban sites in China averaged ˜0.89, while it was significantly higher, ˜0.93, at two relatively rural coastal sites in South Korea and Japan. Differences in fine mode absorption between these regions may result from a combination of factors including aerosol aging during transport, relative humidity differences, sea salt at coastal sites, and fuel type and combustion differences in the two

  10. Analysis of spatial and seasonal distributions of MODIS aerosol optical properties and ground-based measurements of mass concentrations in the Yellow Sea region in 2009.

    PubMed

    Kim, Hak-Sung; Chung, Yong-Seung; Lee, Sun-Gu

    2013-01-01

    Satellite-retrieved data on aerosol optical depth (AOD) and Ångström exponent (AE) using a moderate resolution imaging spectrometer (MODIS) were used to analyze large-scale distributions of atmospheric aerosols in East Asia. AOD was relatively high in March (0.44 ± 0.25) and low in September (0.24 ± 0.21) in the East Asian region in 2009. Sandstorms originating from the deserts and dry areas in northern China and Mongolia were transported on a massive scale during the springtime, thus contributing to the high AOD in East Asia. However, whereas PM10 with diameters ≤10 μm was the highest in February at Anmyon, Cheongwon, and Ulleung, located leeward about halfway through the Korean Peninsula, AOD rose to its highest in May. The growth of hygroscopic aerosols attendant on increases in relative humidity prior to the Asian monsoon season contributed to a high AOD level in May. AE typically appears at high levels (1.30 ± 0.37) in August due to anthropogenic aerosols originating from the industrial areas in eastern China, while AOD stays low in summer due to the removal process caused by rainfall. The linear correlation coefficients of the MODIS AOD and ground-based mass concentrations of PM10 at Anmyon, Cheongwon, and Ulleung were measured at 0.4~0.6. Four cases (6 days) of mineral dustfall from sandstorms and six cases (12 days) of anthropogenically polluted particles were observed in the central area of the Korean Peninsula in 2009. PM10 mass concentrations increased at both Anmyon and Cheongwon in the cases of mineral dustfall and anthropogenically polluted particles. Cases of dustfall from sandstorms and anthropogenic polluted particles, with increasing PM10 mass concentrations, showed higher AOD values in the Yellow Sea region.

  11. Optical and microphysical properties of atmospheric aerosols in Moldova

    NASA Astrophysics Data System (ADS)

    Aculinin, Alexandr; Smicov, Vladimir

    2010-05-01

    Measurements of aerosol properties in Kishinev, Moldova are being carried out within the framework of the international AERONET program managed by NASA/GSFC since 1999. Direct solar and sky diffuse radiances are measured by using of sunphotometer Cimel-318. Aerosol optical properties are retrieved from measured radiances by using of smart computational procedures developed by the AERONET's team. The instrument is situated at the ground-based solar radiation monitoring station giving the opportunity to make simultaneous spectral (win sunphotometer) and broadband (with the set of sensors from radiometric complex) solar radiation. Detailed description of the station and investigations in progress can be found at the http://arg.phys.asm.md. Ground station is placed in an urban environment of Kishinev city (47.00N; 28.56E; 205 m a.s.l). Summary of aerosol optical and microphysical properties retrieved from direct solar and diffuse sky radiance observations at Moldova site from September 1999 to June 2009 are presented below. Number of measurements (total): 1695 Number of measurements (for ?o, n, k): 223 Range of aerosol optical depth (AOD) @440 nm: 0.03 < ?(440) < 2.30, < ?(440)>=0.25 Range of Ångström parameter < α440_870 >: 0.14 < α < 2.28 Asymmetry factor (440/670/870/1020): 0.70/0.63/0.59/0.58 ±0.04 Refraction (n) and absorption (k) indices@440 nm: 1.41 ± 0.06; 0.009 ± 0.005 Single scattering albedo < ?o >(440/670/870/1020): 0.93/0.92/0.90/0.89 ±0.04 Parameters of volume particle size distribution function: (fine mode) volume median radius r v,f , μm: 0.17 ± 0.06 particle volume concentration Cv,f, μm3/μm2: 0.04 ± 0.03 (coarse mode) volume median radius rv,c , μm: 3.08 ± 0.64 particle volume concentration Cv,c, μm3/μm2: 0.03 ± 0.03 Climatic norms of AOD@500 nm and Ångström parameter < α440_870 > at the site of observation are equal to 0.21 ± 0.06 and 1.45 ± 0.14, respectively. The aerosol type in Moldova may be considered as 'urban

  12. Baseline Maritime Aerosol: Methodology to Derive the Optical Thickness and Scattering Properties

    NASA Technical Reports Server (NTRS)

    Kaufman, Yoram J.; Smirnov, Alexander; Holben, Brent N.; Dubovik, Oleg; Einaudi, Franco (Technical Monitor)

    2001-01-01

    Satellite Measurements of the global distribution of aerosol and their effect on climate should be viewed in respect to a baseline aerosol. In this concept, concentration of fine mode aerosol particles is elevated above the baseline by man-made activities (smoke or urban pollution), while coarse mode by natural processes (e.g. dust or sea-spray). Using 1-3 years of measurements in 10 stations of the Aerosol Robotic network (ACRONET we develop a methodology and derive the optical thickness and properties of this baseline aerosol for the Pacific and Atlantic Oceans. Defined as the median for periods of stable optical thickness (standard deviation < 0.02) during 2-6 days, the median baseline aerosol optical thickness over the Pacific Ocean is 0.052 at 500 am with Angstrom exponent of 0.77, and 0.071 and 1.1 respectively, over the Atlantic Ocean.

  13. 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.

  14. Fast Airborne Size Distribution Measurements of an Aerosol Processes and Aging

    NASA Astrophysics Data System (ADS)

    Kapustin, V.; Clarke, A. D.; Zhou, J.; Brekhovskikh, V.; McNaughton, C. S.; Howell, S.

    2009-12-01

    During MILAGRO/INTEX experiment the Hawaii Group for Environmental Aerosol Research (HIGEAR) deployed a wide range of aerosol instrumentation aboard NSF C-130 and NASA DC-8. These were designed to provide rapid information on aerosol composition, state of mixing (internal or external), spectral optical properties (scattering and absorption), the humidity dependence of light scattering - f(RH), and the role of condensed species in changing the absorption properties of black carbon (BC) and inferred properties of organic carbon (OC). We also flew the Fast Mobility Particle Spectrometer (FMPS, TSI Inc.) to measure aerosol size distributions in a range 5.6 - 560 nm. For all our flights around Mexico City, an aerosol number concentration usually was well above the nominal FMPS sensitivity (from ~100 particles/cc @ Dp = 5.6 nm to 1 part/cc @ 560nm), providing us with reliable size distributions even at 1 sec resolution. FMPS measurements revealed small scale structure of an aerosol and allowed us to examine size distributions varying over space and time associated with mixing processes previously unresolved. These 1-Hz measurements during aircraft profiles captured variations in size distributions within shallow layers. Other dynamic processes observed included orography induced aerosol layers and evolution of the nanoparticles formed by nucleation. We put FMPS high resolution size distribution data in a context of aerosol evolution and aging, using a range of established (for MIRAGE/INTEX) chemical, aerosol and transport aging parameters.

  15. 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.

  16. Apparatus for rapid measurement of aerosol bulk chemical composition

    DOEpatents

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

    2003-01-01

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

  17. Apparatus for rapid measurement of aerosol bulk chemical composition

    DOEpatents

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

    2006-04-18

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

  18. Particle Property Data Quality Flags for the MISR Aerosol Product

    NASA Astrophysics Data System (ADS)

    Gaitley, B. J.; Kahn, R. A.; Garay, M. J.

    2012-12-01

    The MISR instrument aboard the NASA Earth Observing System's Terra satellite has the unique capability to retrieve aerosol properties under favorable conditions. General aerosol type retrieval quality guidelines are provided in the MISR Data Quality Statement and related publications. Here we report on the steps we are taking to provide an aerosol-type data quality flag, to be provided with each individual retrieval result. Some factors affecting retrieval quality that can be assessed pre-retrieval are the number of cameras available, the range of scattering angles and surface conditions such as shallow water or seasonal coastal runoff. Factors that must be assessed post-retrieval include low values of retrieved optical depth and the number and type of mixtures successfully passing the MISR algorithm acceptance criteria. Regional monthly plots with MISR measurements binned at 0.5 degree resolution with color-coded stratification of one or more parameters is the main method for identifying locations and times where particle properties are retrieved. Individual MISR values such as mid-visible AOD, number and type of mixtures passing, number of cameras used, the range and maximum scattering angles are plotted individually or as joint distributions. Initially, thresholds and conditions are determined for each MISR parameter separately. Finally, MISR parameters are combined for a given month and region, with their thresholds, to show the overall quality of the retrieval for determining particle properties. Multi-month summaries for more than twelve years of MISR data will aid in assessing quality. Seasons and regions that regularly show poorly constrained aerosol type results are identified, as are times and places where particle property information can be used with confidence. This work is performed in part at the Jet Propulsion Laboratory, California Institute of Technology, under contract with the National Aeronautics and Space Administration and in part at the NASA

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

    NASA Astrophysics Data System (ADS)

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

    2007-06-01

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

  20. Balloon measurements of aerosol in the Antarctic stratosphere

    NASA Technical Reports Server (NTRS)

    Morita, Y.; Takagi, M.; Iwasaka, Y.; Ono, A.

    1985-01-01

    Three balloon soundings of aerosol were conducted from Syowa Station, Antarctica in April, June and October 1983. Number concentration and the size distribution of aerosol particles with diameter greater than 0.3 microns were measured by using a light scattering aerosol particle counter. The influence of the eruption of Mt. El Chichon on the aerosol concentration in the stratosphere was observed on October 16. Very high aerosol concentration at stratospheric heights was obtained from the first successful aerosol sounding in winter Antarctic stratosphere. The result gives direct evidence of winter enhancement in the Antarctic stratosphere.

  1. Coherent Uncertainty Analysis of Aerosol Measurements from Multiple Satellite Sensors

    NASA Technical Reports Server (NTRS)

    Petrenko, M.; Ichoku, C.

    2013-01-01

    Aerosol retrievals from multiple spaceborne sensors, including MODIS (on Terra and Aqua), MISR, OMI, POLDER, CALIOP, and SeaWiFS altogether, a total of 11 different aerosol products were comparatively analyzed using data collocated with ground-based aerosol observations from the Aerosol Robotic Network (AERONET) stations within the Multi-sensor Aerosol Products Sampling System (MAPSS, http://giovanni.gsfc.nasa.gov/mapss/ and http://giovanni.gsfc.nasa.gov/aerostat/). The analysis was performed by comparing quality-screened satellite aerosol optical depth or thickness (AOD or AOT) retrievals during 2006-2010 to available collocated AERONET measurements globally, regionally, and seasonally, and deriving a number of statistical measures of accuracy. We used a robust statistical approach to detect and remove possible outliers in the collocated data that can bias the results of the analysis. Overall, the proportion of outliers in each of the quality-screened AOD products was within 12%. Squared correlation coefficient (R2) values of the satellite AOD retrievals relative to AERONET exceeded 0.6, with R2 for most of the products exceeding 0.7 over land and 0.8 over ocean. Root mean square error (RMSE) values for most of the AOD products were within 0.15 over land and 0.09 over ocean. We have been able to generate global maps showing regions where the different products present advantages over the others, as well as the relative performance of each product over different landcover types. It was observed that while MODIS, MISR, and SeaWiFS provide accurate retrievals over most of the landcover types, multi-angle capabilities make MISR the only sensor to retrieve reliable AOD over barren and snow / ice surfaces. Likewise, active sensing enables CALIOP to retrieve aerosol properties over bright-surface shrublands more accurately than the other sensors, while POLDER, which is the only one of the sensors capable of measuring polarized aerosols, outperforms other sensors in

  2. Stackable differential mobility analyzer for aerosol measurement

    DOEpatents

    Cheng, Meng-Dawn; Chen, Da-Ren

    2007-05-08

    A multi-stage differential mobility analyzer (MDMA) for aerosol measurements includes a first electrode or grid including at least one inlet or injection slit for receiving an aerosol including charged particles for analysis. A second electrode or grid is spaced apart from the first electrode. The second electrode has at least one sampling outlet disposed at a plurality different distances along its length. A volume between the first and the second electrode or grid between the inlet or injection slit and a distal one of the plurality of sampling outlets forms a classifying region, the first and second electrodes for charging to suitable potentials to create an electric field within the classifying region. At least one inlet or injection slit in the second electrode receives a sheath gas flow into an upstream end of the classifying region, wherein each sampling outlet functions as an independent DMA stage and classifies different size ranges of charged particles based on electric mobility simultaneously.

  3. 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.

  4. Vertical Profile of Aerosol Properties at Pico Mountain, Azores

    NASA Astrophysics Data System (ADS)

    Wright, K.; Mazzoleni, C.; Mazzoleni, L. R.; Dzepina, K.; Hueber, J.; China, S.; Sharma, N.

    2013-12-01

    Pico Mountain (2325m asl) is a dormant volcano in the archipelago of the Azores1500 km west of Lisbon, Portugal in the North Atlantic. It differs from typical mountain ranges such as the Alps or the Rockies, which are large and present a complex orography. Pico Mountain has a simple cone-like structure with only one main peak and is thousands of kilometers away from any other significant mountain range. In summer months, it is typical for air masses to move around the mountain rather than traveling up its face. This implies that often the peak of the mountain lies above the marine boundary layer in the free troposphere, while the lower part of the mountain is affected by marine clouds and marine air-masses. An atmospheric monitoring station, the Pico Mountain Observatory was established in 2001 in the summit caldera of the volcano at 2225m above sea level. The observatory is far from large populations or pollution sources, which makes the station ideal to study atmospheric gases and aerosols transported over long-ranges in the free troposphere. The station is reachable only by foot following a steep and strenuous hiking trail. In the summer of 2013 we began to collect vertical profiles of aerosol by carrying an instrumented backpack up to the summit of the mountain, with the goal of studying the vertical structure of atmospheric aerosols from the marine boundary layer to the free troposphere. The backpack was carried from the base of trail at 1200m asl. The backpack was equipped with the following instruments: 1. Nephelometer to measure light scattering from aerosol 2. 2-size optical particle counter (300-500 nm) 3. Portable micro-aethalometer to measure absorbing aerosols 4. SEM/TEM sampler to collect particles for off-line electron microscopy analysis 5. Battery powered data logger to measure relative humidity, temperature and pressure 6. GPS tracking device We provide a preliminary analysis of data collected in 2013 to gain insight on the vertical distribution

  5. Microphysical properties of transported biomass burning aerosols in coastal regions, and application to improving retrievals of aerosol optical depth from SeaWiFS data

    NASA Astrophysics Data System (ADS)

    Sayer, A. M.; Hsu, N. C.; Bettenhausen, C.

    2013-05-01

    Due to the limited measurement capabilities of heritage and current spaceborne passive imaging radiometers, algorithms for the retrieval of aerosol optical depth (AOD) and related quantities must make assumptions relating to aerosol microphysical properties and surface reflectance. Over the ocean, surface reflectance can be relatively well-modelled, but knowledge of aerosol properties can remain elusive. Several field campaigns and many studies have examined the microphysical properties of biomass burning (smoke) aerosol. However, these largely focus on properties over land and near to the source regions. In coastal and open-ocean regions the properties of transported smoke may differ, due to factors such as aerosol aging, wet/dry deposition, and mixture with other aerosol sources (e.g. influence of maritime, pollution, or mineral dust aerosols). Hence, models based on near-source aerosol observations may be less representative of such transported smoke aerosols, introducing additional uncertainty into satellite retrievals of aerosol properties. This study examines case studies of transported smoke from select globally-distributed coastal and island Aerosol Robotic Network (AERONET) sites. These are used to inform improved models for over-ocean transported smoke aerosol for AOD retrievals from the Sea-viewing Wide Field-of-view Sensor (SeaWiFS). These models are used in an updated version of the SeaWiFS Ocean Aerosol Retrieval (SOAR) algorithm, which has been combined with the Deep Blue algorithm over land to create a 13-year (1997-2010) high-quality record of AOD over land and ocean. Applying these algorithms to other sensors will enable the creation of a long-term global climate data record of spectral AOD.

  6. A closure study of aerosol optical properties at a regional background mountainous site in Eastern China.

    PubMed

    Yuan, Liang; Yin, Yan; Xiao, Hui; Yu, Xingna; Hao, Jian; Chen, Kui; Liu, Chao

    2016-04-15

    There is a large uncertainty in evaluating the radiative forcing from aerosol-radiation and aerosol-cloud interactions due to the limited knowledge on aerosol properties. In-situ measurements of aerosol physical and chemical properties were carried out in 2012 at Mt. Huang (the Yellow Mountain), a continental background mountainous site in eastern China. An aerosol optical closure study was performed to verify the model outputs by using the measured aerosol optical properties, in which a spherical Mie model with assumptions of external and core-shell mixtures on the basis of a two-component optical aerosol model and high size-segregated element carbon (EC) ratio was applied. Although the spherical Mie model would underestimate the real scattering with increasing particle diameters, excellent agreement between the calculated and measured values was achieved with correlation coefficients above 0.98. Sensitivity experiments showed that the EC ratio had a negligible effect on the calculated scattering coefficient, but largely influenced the calculated absorption coefficient. The high size-segregated EC ratio averaged over the study period in the closure was enough to reconstruct the aerosol absorption coefficient in the Mie model, indicating EC size resolution was more important than time resolution in retrieving the absorption coefficient in the model. The uncertainties of calculated scattering and absorption coefficients due to the uncertainties of measurements and model assumptions yielded by a Monte Carlo simulation were ±6% and ±14% for external mixture and ±9% and ±31% for core-shell mixture, respectively. This study provided an insight into the inherent relationship between aerosol optical properties and physicochemical characteristics in eastern China, which could supplement the database of aerosol optical properties for background sites in eastern China and provide a method for regions with similar climate.

  7. Transported acid aerosols measured in southern Ontario

    NASA Astrophysics Data System (ADS)

    Keeler, Gerald J.; Spengler, John D.; Koutrakis, Petros; Allen, George A.; Raizenne, Mark; Stern, Bonnie

    During the period 29 June 1986-9 August 1986, a field health study assessing the acute health effects of air pollutants on children was conducted at a summer girls' camp on the northern shore of Lake Erie in SW Ontario. Continuous air pollution measurements of SO 2, O 3, NO x, particulate sulfates, light scattering, and meteorological measurements including temperature, dew point, and wind speed and direction were made. Twelve-hour integrated samples of size fractioned particles were also obtained using dichotomous samplers and Harvard impactors equipped with an ammonia denuder for subsequent hydrogen ion determination. Particulate samples were analyzed for trace elements by X-ray fluorescence and Neutron Activation, and for organic and elemental carbon by a thermal/optical technique. The measured aerosol was periodically very acidic with observed 12-h averaged H + concentrations in the range < 10-560 nmoles m -3. The aerosol H + appeared to represent the net strong acidity after H 2SO 4 reaction with NH 3(g). Average daytime concentrations were higher than night-time for aerosol H +, sulfate, fine mass and ozone. Prolonged episodes of atmospheric acidity, sulfate, and ozone were associated with air masses arriving at the measurement site from the west and from the southwest over Lake Erie. Sulfate concentrations measured at the lakeshore camp were more than twice those measured at inland sites during extreme pollution episodes. The concentration gradient observed with onshore flow was potentially due to enhanced deposition near the lakeshore caused by discontinuities in the meteorological fields in this region.

  8. Street canyon aerosol pollutant transport measurements.

    PubMed

    Longley, I D; Gallagher, M W; Dorsey, J R; Flynn, M; Bower, K N; Allan, J D

    2004-12-01

    Current understanding of dispersion in street canyons is largely derived from relatively simple dispersion models. Such models are increasingly used in planning and regulation capacities but are based upon a limited understanding of the transport of substances within a real canyon. In recent years, some efforts have been made to numerically model localised flow in idealised canyons (e.g., J. Appl. Meteorol. 38 (1999) 1576-89) and stepped canyons (Assimakopoulos V. Numerical modelling of dispersion of atmospheric pollution in and above urban canopies. PhD thesis, Imperial College, London, 2001) but field studies in real canyons are rare. To further such an understanding, a measurement campaign has been conducted in an asymmetric street canyon with busy one-way traffic in central Manchester in northern England. The eddy correlation method was used to determine fluxes of size-segregated accumulation mode aerosol. Measurements of aerosol at a static location were made concurrently with measurements on a platform lift giving vertical profiles. Size-segregated measurements of ultrafine and coarse particle concentrations were also made simultaneously at various heights. In addition, a small mobile system was used to make measurements of turbulence at various pavement locations within the canyon. From this data, various features of turbulent transport and dispersion in the canyon will be presented. The concentration and the ventilation fluxes of vehicle-related aerosol pollutants from the canyon will be related to controlling factors. The results will also be compared with citywide ventilation data from a separate measurement campaign conducted above the urban canopy.

  9. Aerosol-cloud closure study using RPAS measurements

    NASA Astrophysics Data System (ADS)

    Calmer, R.; Roberts, G.; Sanchez, K. J.; Nicoll, K.; Preissler, J.; Ovadnevaite, J.; Sciare, J.; Bronz, M.; Hattenberger, G.; Rosenfeld, D.; Lauda, S.; Hashimshoni, E.

    2015-12-01

    Enhancements in Remotely Piloted Aircraft Systems (RPAS) have increased their possible uses in many fields for the past two decades. For atmospheric research, ultra-light RPAS (< 2.5kg) are now able to fly at altitudes greater than 3 km and even in cloud, which opens new opportunities to understand aerosol-cloud interactions. We are deploying the RPAS as part of the European project BACCHUS (Impact of Biogenic versus Anthropogenic Emissions on Clouds and Climate: towards a Holistic Understanding). Field experiments in Cyprus and Ireland have already been conducted to study aerosol-cloud interactions in climatically different environments. The RPAS are being utilized in this study with the purpose of complementing ground-based observations of cloud condensation nuclei (CCN) to conduct aerosol-cloud closure studies Cloud microphysical properties such as cloud drop number concentration and size can be predicted directly from the measured CCN spectrum and the observed updraft, the vertical component of the wind vector [e.g., Conant et al, 2004]. On the RPAS, updraft measurements are obtained from a 5-hole probe synchronized with an Inertial Measurement Unit (IMU). The RPA (remotely piloted aircraft) are programmed to fly at a level leg just below cloud base to measure updraft measurements while a scanning CCN counter is stationed at ground level. Vertical profiles confirm that CCN measurements on the ground are representative to those at cloud base. An aerosol-cloud parcel model is implemented to model the cloud droplet spectra associated with measured updraft velocities. The model represents the particle size domain with internally mixed chemical components, using a fixed-sectional approach [L. M. Russell and Seinfeld, 1998]. The model employs a dual moment (number and mass) algorithm to calculate growth of particles from one section to the next for non-evaporating species. Temperature profiles, cloud base, updraft velocities and aerosol size and composition, all

  10. Coarse mode aerosol measurement using a Low Turbulence Inlet

    NASA Astrophysics Data System (ADS)

    Brooke, J.; Bart, M.; Trembath, J.; McQuaid, J. B.; Brooks, B. J.; Osborne, S.

    2012-04-01

    The Sahara desert is a major natural source of global mineral dust emissions (Forster et al., 2007) through the mobilisation and lifting of dust particles into the atmosphere from dust storms. A significant fraction of this dust is in the aerosol coarse mode (Weinzierl et al., 2009). It is highlighted of the difficulty in making accurate and reliable measurements from an aircraft platform, particularly that of coarse mode aerosol (Wendisch et al., 2004). To achieve the measurement of a representative aerosol sample an aerosol inlet, on an aircraft, is required for the delivery of the sample to the instruments making the measurements. Inlet design can modify aerosol size distribution through either underestimating due to aerosol losses or overestimation due to enhancements. The Low Turbulence Inlet (LTI) was designed to improve inlet efficiency. This is achieved by reducing turbulence flow within the tip of the inlet, reducing impaction of particles to the walls of the inlet (Wilson et al., 2004). The LTI further maintains isokinetic sampling flow (free stream velocity, U0 and sampling velocity, U are equal to 1). Dust aerosol over the Sahara desert provides an excellent environment to test and quantify the capabilities of the LTI on the FAAM BAe 146, whilst enabling in-situ dust measurement. The LTI was operated during the Fennec field campaign in June 2011 with 11 flights during the campaign over Mauritania and Mali. We are using the LTI to provide critical information on the sampling characteristics of the inlet used by nearly all aerosol instruments inside the aircraft (AMS, Nephelometer, PSAP, and CCN). Inlet experiments were performed with identical Optical Particle Counters (OPC) connected to the rosemount and LTI with size distribution for each inlet measured and Rosemount enhancements determined. Rosemount inlet enhancements were determined to be 2 to 4 times for particles up to 2.5 µm. A key parameter in aerosol measurement is size distribution, in which

  11. Simultaneous Retrieval of Aerosol and Cloud Properties During the MILAGRO Field Campaign

    NASA Technical Reports Server (NTRS)

    Knobelspiesse, K.; Cairns, B.; Redemann, J.; Bergstrom, R. W.; Stohl, A.

    2011-01-01

    Estimation of Direct Climate Forcing (DCF) due to aerosols in cloudy areas has historically been a difficult task, mainly because of a lack of appropriate measurements. Recently, passive remote sensing instruments have been developed that have the potential to retrieve both cloud and aerosol properties using polarimetric, multiple view angle, and multi spectral observations, and therefore determine DCF from aerosols above clouds. One such instrument is the Research Scanning Polarimeter (RSP), an airborne prototype of a sensor on the NASA Glory satellite, which unfortunately failed to reach orbit during its launch in March of 2011. In the spring of 2006, the RSP was deployed on an aircraft based in Veracruz, Mexico, as part of the Megacity Initiative: Local and Global Research Observations (MILAGRO) field campaign. On 13 March, the RSP over flew an aerosol layer lofted above a low altitude marine stratocumulus cloud close to shore in the Gulf of Mexico. We investigate the feasibility of retrieving aerosol properties over clouds using these data. Our approach is to first determine cloud droplet size distribution using the angular location of the cloud bow and other features in the polarized reflectance. The selected cloud was then used in a multiple scattering radiative transfer model optimization to determine the aerosol optical properties and fine tune the cloud size distribution. In this scene, we were able to retrieve aerosol optical depth, the fine mode aerosol size distribution parameters and the cloud droplet size distribution parameters to a degree of accuracy required for climate modeling. This required assumptions about the aerosol vertical distribution and the optical properties of the coarse aerosol size mode. A sensitivity study was also performed to place this study in the context of future systematic scanning polarimeter observations, which found that the aerosol complex refractive index can also be observed accurately if the aerosol optical depth is

  12. Morphology and Optical Properties of Mixed Aerosol Particles

    NASA Astrophysics Data System (ADS)

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

    2015-04-01

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

  13. Elemental Composition of Primary Aerosols Emitted from Burning of 21 Biomass Fuels Measured by Aerosol Mass Spectrometer

    NASA Astrophysics Data System (ADS)

    Desyaterik, Y.; Mack, L.; Lee, T.; Kreidenweis, S. M.; Collett, J. L.; Jimenez, J. L.; Worsnop, D. R.

    2010-12-01

    Biomass burning emissions are an important contributor to regional aerosol loading and have a large impact of on air quality, visibility, and radiative forcing. However, the detailed chemical composition of the aerosols emitted during biomass burning is largely unknown. In order to gain a better understanding of the chemical and physical properties of these emissions, 92 burns were undertaken in the combustion chamber of the USDA/FS Fire Sciences Laboratory in Missoula, Montana, in well-defined laboratory conditions. A set of 21 different fuels was tested that represents biomass burned annually in the western and southeastern U.S. The chemical composition of the resulting biomass smoke aerosols was analyzed with a high-resolution aerosol mass spectrometer (Aerodyne HR-ToF-AMS). Simultaneous measurements of CO2 and CO concentrations allowed flaming and smoldering fire regimes to be distinguished. The elemental composition of the organic portion of the aerosols was extracted from the AMS measurements. Here we present the variation of O/C, H/C and organic mass to organic carbon ratios (OM/OC) versus fire regime and fuel type. We also discuss the influence on the organic aerosol chemical composition of various factors such as fuel moisture content and total aerosol loading, as well as the approach used to account for water vapor ions derived from water originally present in sampled particles versus water vapor ions produced by electron impact fragmentation of organic molecules.

  14. Aerosol properties and associated radiative effects over Cairo (Egypt)

    NASA Astrophysics Data System (ADS)

    El-Metwally, M.; Alfaro, S. C.; Wahab, M. M. Abdel; Favez, O.; Mohamed, Z.; Chatenet, B.

    2011-02-01

    Cairo is one of the largest megacities in the World and the particle load of its atmosphere is known to be particularly important. In this work we aim at assessing the temporal variability of the aerosol's characteristics and the magnitude of its impacts on the transfer of solar radiation. For this we use the level 2 quality assured products obtained by inversion of the instantaneous AERONET sunphotometer measurements performed in Cairo during the Cairo Aerosol CHaracterization Experiment (CACHE), which lasted from the end of October 2004 to the end of March 2006. The analysis of the temporal variation of the aerosol's optical depth (AOD) and spectral dependence suggests that the aerosol is generally a mixture of at least 3 main components differing in composition and size. This is confirmed by the detailed analysis of the monthly-averaged size distributions and associated optical properties (single scattering albedo and asymmetry parameter). The components of the aerosol are found to be 1) a highly absorbing background aerosol produced by daily activities (traffic, industry), 2) an additional, 'pollution' component produced by the burning of agricultural wastes in the Nile delta, and 3) a coarse desert dust component. In July, an enhancement of the accumulation mode is observed due to the atmospheric stability favoring its building up and possibly to secondary aerosols being produced by active photochemistry. More generally, the time variability of the aerosol's characteristics is due to the combined effects of meteorological factors and seasonal production processes. Because of the large values of the AOD achieved during the desert dust and biomass burning episodes, the instantaneous aerosol radiative forcing (RF) at both the top (TOA) and bottom (BOA) of the atmosphere is maximal during these events. For instance, during the desert dust storm of April 8, 2005 RF BOA, RF TOA, and the corresponding atmospheric heating rate peaked at - 161.7 W/m 2, - 65.8 W/m 2

  15. Retrieving the Vertical Structure of the Effective Aerosol Complex Index of Refraction from a Combination of Aerosol in Situ and Remote Sensing Measurements During TARFOX

    NASA Technical Reports Server (NTRS)

    Redemann, J.; Turco, R. P.; Liou, K. N.; Russell, P. B.; Bergstrom, R. W.; Schmid, B.; Livingston, J. M.; Hobbs, P. V.; Hartley, W. S.; Ismail, S.; Ferrare, R. A.; Browell, E. V.

    2000-01-01

    The largest uncertainty in estimates of the effects of atmospheric aerosols on climate stems from uncertainties in the determination of their microphysical properties, including the aerosol complex index of refraction, which in turn determines their optical properties. A novel technique is used to estimate the aerosol complex index of refraction in distinct vertical layers from a combination of aerosol in situ size distribution and remote sensing measurements during the Tropospheric Aerosol Radiative Forcing Observational Experiment (TARFOX). In particular, aerosol backscatter measurements using the NASA Langley LASE (Lidar Atmospheric Sensing Experiment) instrument and in situ aerosol size distribution data are utilized to derive vertical profiles of the "effective" aerosol complex index of refraction at 815 nm (i.e., the refractive index that would provide the same backscatter signal in a forward calculation on the basis of the measured in situ particle size distributions for homogeneous, spherical aerosols). A sensitivity study shows that this method yields small errors in the retrieved aerosol refractive indices, provided the errors in the lidar-derived aerosol backscatter are less than 30% and random in nature. Absolute errors in the estimated aerosol refractive indices are generally less than 0.04 for the real part and can be as much as 0.042 for the imaginary part in the case of a 30% error in the lidar-derived aerosol backscatter. The measurements of aerosol optical depth from the NASA Ames Airborne Tracking Sunphotometer (AATS-6) are successfully incorporated into the new technique and help constrain the retrieved aerosol refractive indices. An application of the technique to two TARFOX case studies yields the occurrence of vertical layers of distinct aerosol refractive indices. Values of the estimated complex aerosol refractive index range from 1.33 to 1.45 for the real part and 0.001 to 0.008 for the imaginary part. The methodology devised in this study

  16. Analysis of aerosol properties derived from sun photometer and lidar over Dunhuang radiometric calibration site

    NASA Astrophysics Data System (ADS)

    Chen, Lin; Jing, Yingying; Zhang, Peng; Hu, Xiuqing

    2016-05-01

    Duhuang site has been selected as China Radiation Calibration Site (CRCS) for Remote Sensing Satellite Sensors since 1996. With the economic development of Dunhuang city, the ambient of the radiation calibration field has changed in recent years. Taking into account the key role of aerosol in radiometric calibration, it is essential to investigate the aerosol optical properties over Dunhuang radiometric calibration site. In this paper, the CIMEL sun photometer (CE-318) and Mie-scattering Lidar are simultaneously used to measure aerosol optical properties in Dunhuang site. Data from aerosol-bands of sun photometer are used in a Langley method to determine spectral optical depths of aerosol. And Lidar is utilized to obtain information of vertical profile and integrated aerosol optical depths at different heights. The results showed that the aerosol optical depth at 500 nm wavelength during the in-situ measurement campaigns varied from 0.1 to 0.3 in Dunhuang site. And the observation results also indicated that high aerosol concentration layer mostly located at the height of about 2~4 km. These results implies that the aerosol concentration of atmosphere in Dunhuang was relatively small and suitable for in-flight calibration for remote sensing satellite sensors.

  17. North Atlantic Aerosol Properties and Direct Radiative Effects: Key Results from TARFOX and ACE-2

    NASA Technical Reports Server (NTRS)

    Russell, P. B.; Livingston, J. M.; Schmid, B.; Bergstrom, R. A.; Hignett, P.; Hobbs, P. V.; Durkee, P. A.; Condon, Estelle (Technical Monitor)

    1998-01-01

    Aerosol effects on atmospheric radiative fluxes provide a forcing function that can change the climate in potentially significant ways. This aerosol radiative Forcing is a major source of uncertainty in understanding the observed climate change of the past century and in predicting, future climate. To help reduce this uncertainty, the International Global Atmospheric Chemistry Project (IGAC) has endorsed a series of multiplatform aerosol field campaigns. The Tropospheric Aerosol Radiative Forcing Observational Experiment (TARFOX) and the second Aerosol Characterization Experiment (ACE-2) were the first IGAC campaigns to address the impact of anthropogenic aerosols. Both TARFOX and ACE-2 gathered extensive data sets on aerosol properties and radiative effects. TARFOX focused on the urban-industrial haze plume flowing from the eastern United States over the western Atlantic Ocean, whereas ACE-2 studied aerosols carried over the eastern Atlantic from both European urban/industrial and African mineral sources. These aerosols often have a marked influence on the top-of-atmosphere radiances measured by satellites, as illustrated in Figure 1. Shown there are contours of aerosol optical depth derived from radiances measured by the AVHRR sensor on the NOAA-11 satellite. The contours readily show that aerosols originating in North America, Europe, and Africa impact the radiative properties of air over the North Atlantic. However, the accurate derivation of flux chances, or radiative forcing, from the satellite-measured radiances or 'etrieved optical depths remains a difficult challenge. In this paper we summarize key Initial results from TARFOX and, to a lesser extent ACE-2, with a focus on those results that allow an improved assessment of the flux changes caused by North Atlantic aerosols at middle and high latitudes.

  18. North Atlantic Aerosol Properties and Direct Radiative Effects: Key Results from TARFOX and ACE-2

    NASA Technical Reports Server (NTRS)

    Russell, P. B.; Livingston, J. M.; Schmid, B.; Bergstrom, Robert A.; Hignett, P.; Hobbs, P. V.; Durkee, P. A.

    2000-01-01

    Aerosol effects on atmospheric radiative fluxes provide a forcing function that can change the climate In potentially significant ways. This aerosol radiative forcing is a major source of uncertainty in understanding the observed climate change of the past century and in predicting future climate. To help reduce this uncertainty, the International Global Atmospheric Chemistry Project (IGAC) has endorsed a series of multiplatform aerosol field campaigns. The Tropospheric Aerosol Radiative Forcing Observational Experiment (TARFOX) and the second Aerosol Characterization Experiment (ACE-2) were the first IGAC campaigns to address the impact of anthropogenic aerosols, Both TARFOX and ACE-2 gathered extensive data sets on aerosol properties and radiative effects, TARFOX focused on the urban-industrial haze plume flowing from the eastern United States over the western Atlantic Ocean, whereas ACE-2 studied aerosols carried over the eastern Atlantic from both European urban/industrial and African mineral sources. These aerosols often have a marked influence on the top-of-atmosphere radiances measured by satellites. Shown there are contours of aerosol optical depth derived from radiances measured by the AVHRR sensor on the NOAA-11 satellite. The contours readily show that aerosols originating in North America, Europe, and Africa impact the radiative properties of air over the North Atlantic. However, the accurate derivation of flux changes, or radiative forcing, from the satellite measured radiances or retrieved optical depths remains a difficult challenge. In this paper we summarize key initial results from TARFOX and, to a lesser extent, ACE-2, with a focus on those results that allow an improved assessment of the flux changes caused by North Atlantic aerosols at middle latitudes.

  19. Synthesis of information on aerosol optical properties

    NASA Astrophysics Data System (ADS)

    Liu, Hongqing; Pinker, R. T.; Chin, M.; Holben, B.; Remer, L.

    2008-04-01

    In a previous study (Liu et al., 2005) obtained are global scale estimates of aerosol optical depth at 0.55 μm based on spatial and temporal variation patterns from models and satellite observations, regulated by the Aerosol Robotic Network (AERONET) measurements. In this study an approach is developed to obtain information on global distribution of the single scattering albedo (ω0), the asymmetry parameter (g), and the normalized extinction coefficient over shortwave (SW) spectrum. Since space observations of ω0 are in early stages of development and none are available for g, first an approach was developed to infer them from relevant information from the Global Ozone Chemistry Aerosol Radiation and Transport (GOCART) model, Moderate Resolution Imaging Spectroradiometer (MODIS) and AERONET retrievals. The single scattering albedo is generated by extending GOCART ω0 at 0.55 μm to the entire SW spectrum using spectral dependence derived from AERONET retrievals. The asymmetry parameter over the solar spectrum is derived from the MODIS Ångström wavelength exponent, utilizing a relationship based on AERONET almucantar observations. The normalized extinction coefficient is estimated from the MODIS Ångström wavelength exponent. The methodology was implemented as a "proof of concept" with one year of data. The approach described here is a step in preparedness for utilizing information from new observing systems (e.g., MISR, A-Train constellation) when available. The impact of the newly derived information on the quality of satellite based estimates of surface radiative fluxes was evaluated and is presented by Liu and Pinker (2008).

  20. Raman lidar measurements of aerosol extinction and backscattering 1. Methods and comparisons

    SciTech Connect

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

    1998-08-01

    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 0.015 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 0.1 and 5 km are found to be about 10{endash}40{percent} 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{percent} 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. {copyright} 1998 American Geophysical Union

  1. 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.

  2. Aerosol Profile Measurements from the NASA Langley Research Center Airborne High Spectral Resolution Lidar

    NASA Technical Reports Server (NTRS)

    Obland, Michael D.; Hostetler, Chris A.; Ferrare, Richard A.; Hair, John W.; Roers, Raymond R.; Burton, Sharon P.; Cook, Anthony L.; Harper, David B.

    2008-01-01

    Since achieving first light in December of 2005, the NASA Langley Research Center (LaRC) Airborne High Spectral Resolution Lidar (HSRL) has been involved in seven field campaigns, accumulating over 450 hours of science data across more than 120 flights. Data from the instrument have been used in a variety of studies including validation and comparison with the Cloud- Aerosol Lidar and Infrared Pathfinder Satellite Observation (CALIPSO) satellite mission, aerosol property retrievals combining passive and active instrument measurements, aerosol type identification, aerosol-cloud interactions, and cloud top and planetary boundary layer (PBL) height determinations. Measurements and lessons learned from the HSRL are leading towards next-generation HSRL instrument designs that will enable even further studies of aerosol intensive and extensive parameters and the effects of aerosols on the climate system. This paper will highlight several of the areas in which the NASA Airborne HSRL is making contributions to climate science.

  3. Optical properties and radiative forcing of urban aerosols in Nanjing, China

    NASA Astrophysics Data System (ADS)

    Zhuang, B. L.; Wang, T. J.; Li, S.; Liu, J.; Talbot, R.; Mao, H. T.; Yang, X. Q.; Fu, C. B.; Yin, C. Q.; Zhu, J. L.; Che, H. Z.; Zhang, X. Y.

    2014-02-01

    Continuous measurements of atmospheric aerosols were made in Nanjing, a megacity in China, from 18 January to 18 April, 2011 (Phase 1) and from 22 April 2011 to 21 April 2012 (Phase 2). Aerosol characteristics, optical properties, and direct radiative forcing (DRF) were studied through interpretations of these measurements. We found that during Phase 1, mean PM2.5, black carbon (BC), and aerosol scattering coefficient (Bsp) in Nanjing were 76.1 ± 59.3 μg m-3, 4.1 ± 2.2 μg m-3, and 170.9 ± 105.8 M m-1, respectively. High pollution episodes occurred during Spring and Lantern Festivals when hourly PM2.5 concentrations reached 440 μg m-3, possibly due to significant discharge of fireworks. Temporal variations of PM2.5, BC, and Bsp were similar to each other. It is estimated that inorganic scattering aerosols account for about 49 ± 8.6% of total aerosols while BC only accounted for 6.6 ± 2.9%, and nitrate was larger than sulfate. In Phase 2, optical properties of aerosols show great seasonality. High relative humidity (RH) in summer (June, July, August) likely attributed to large optical depth (AOD) and small Angstrom exponent (AE) of aerosols. Due to dust storms, AE of total aerosols was the smallest in spring (March, April, May). Annual mean 550-nm AOD and 675/440-nm AE were 0.6 ± 0.3 and 1.25 ± 0.29 for total aerosols, 0.04 ± 0.02 and 1.44 ± 0.50 for absorbing aerosols, 0.48 ± 0.29 and 1.64 ± 0.29 for fine aerosols, respectively. Annual single scattering albedo of aerosols ranged from 0.90 to 0.92. Real time wavelength-dependent surface albedo from the Moderate Resolution Imaging Spectroradiometer (MODIS) was used to assess aerosol DRFs. Both total and absorbing aerosol DRFs had significant seasonal variations in Nanjing and they were the strongest in summer. Annual mean clear sky TOA DRF (including daytime and nighttime) of total and absorbing aerosols was about -6.9 and +4.5 W m-2, respectively. Aerosol DRFs were found to be sensitive to surface

  4. Stratospheric Aerosol Extinction Retrieval for SCIAMACHY Measurements in Limb Geometry

    NASA Astrophysics Data System (ADS)

    Dörner, S.; Pukite, J.; Penning de Vries, M.; Beirle, S.; Wagner, T.

    2015-12-01

    Techniques for retrieving height resolved information on stratospheric aerosol improved significantly in the past decade with the availability of satellites measurements in limb geometry. Instruments like OMPS, OSIRIS and SCIAMACHY provide height resolved radiance spectra with global coverage. Long term data sets of stratospheric aerosol extinction profiles are important for a detailed investigation of spatial and temporal variation and formation processes (e.g. after volcanic eruptions or in polar stratospheric clouds). Resulting data sets contain vital information for climate models (radiative effect) or chemistry models (reaction surface for heterogeneous chemistry). This study focuses on the SCIAMACHY instrument which measured scattered sunlight in the ultra violet, visible and near infra red spectral range between 2002 and 2012. SCIAMACHY's unique method of alternating measurements in limb and nadir geometry provides co-located profile and column information respectively that can be used to characterize plumes with small horizontal extents. The covered wavelength range potentially provides information on effective micro-physical properties of the aerosol particles. However, scattering on background aerosol constitutes only a small fraction of detected radiance and assumptions on particle characteristics (e.g., size distribution) have to be made which results in potential uncertainties especially for wavelengths below 700 nm and for measurements in backscatter geometry. Methods to reduce these uncertainties are investigated and applied to our newly developed retrieval algorithm. In addition, so called spatial straylight contamination of the measured signal was identified as a significant error source and an empirical correction scheme was developed. Comparisons with SAGE II measurement in occultation geometry and balloon borne measurements with an optical particle counter confirm the viability of our retrieval algorithm.

  5. Estimation of aerosol direct forcing by Asian dust using sun/sky radiometer and lidar measurement

    NASA Astrophysics Data System (ADS)

    Won, J. G.; Yoon, S. C.; Holben, B.

    2002-12-01

    Appropriate optical parameters of aerosols are critical part for estimating aerosol direct forcing. We suggest a method of determining aerosol parameters for the radiative transfer model, CRM released by NCAR, from AERONET inversion data set. AERONET inversion provides size distribution and complex refractive indices at 4 wavelengths, 440, 670, 870 and 1020nm. Mie calculation can produce the aerosol optical parameters, such as aerosol optical thickness (AOT), single scattering albedo (SSA), asymmetry factor(g) and by using regression fitting method on log-log plane, the parameters at 19 channels of short wavelength region can be retrieved. With this method, it becomes possible to use ground-base solar radiance measurement data for calculating aerosol direct forcing without assuming the specific aerosol type in advance. We investigated the differences of aerosol forcing by dust and non-dust aerosols. Out of AERONET data collected in Apr. 2001, the properties of Asian dust aerosols were examined, which have the characteristics of bigger AOT, bigger SSA (bigger solar radiance reflection) and less wavelength dependence of SSA and g. This difference makes larger aerosol direct forcing at TOA and less atmospheric absorption. The aerosol profiles measured by lidar are also applied for radiative transfer calculation. The profiles of short wave radiation flux and heating rate by dust were investigated for two Asian dust events, one was elevated dust event and the other was dust event settling into the PBL. Instantaneous heating rate larger than 2K/day was estimated within dust aerosol layer and several differences of radiation flux profiles due to the aerosol profiles were investigated.

  6. Development and first application of an Aerosol Collection Module (ACM) for quasi online compound specific aerosol measurements

    NASA Astrophysics Data System (ADS)

    Hohaus, Thorsten; Kiendler-Scharr, Astrid; Trimborn, Dagmar; Jayne, John; Wahner, Andreas; Worsnop, Doug

    2010-05-01

    Atmospheric aerosols influence climate and human health on regional and global scales (IPCC, 2007). In many environments organics are a major fraction of the aerosol influencing its properties. Due to the huge variety of organic compounds present in atmospheric aerosol current measurement techniques are far from providing a full speciation of organic aerosol (Hallquist et al., 2009). The development of new techniques for compound specific measurements with high time resolution is a timely issue in organic aerosol research. Here we present first laboratory characterisations of an aerosol collection module (ACM) which was developed to allow for the sampling and transfer of atmospheric PM1 aerosol. The system consists of an aerodynamic lens system focussing particles on a beam. This beam is directed to a 3.4 mm in diameter surface which is cooled to -30 °C with liquid nitrogen. After collection the aerosol sample can be evaporated from the surface by heating it to up to 270 °C. The sample is transferred through a 60cm long line with a carrier gas. In order to test the ACM for linearity and sensitivity we combined it with a GC-MS system. The tests were performed with octadecane aerosol. The octadecane mass as measured with the ACM-GC-MS was compared versus the mass as calculated from SMPS derived total volume. The data correlate well (R2 0.99, slope of linear fit 1.1) indicating 100 % collection efficiency. From 150 °C to 270 °C no effect of desorption temperature on transfer efficiency could be observed. The ACM-GC-MS system was proven to be linear over the mass range 2-100 ng and has a detection limit of ~ 2 ng. First experiments applying the ACM-GC-MS system were conducted at the Jülich Aerosol Chamber. Secondary organic aerosol (SOA) was formed from ozonolysis of 600 ppbv of b-pinene. The major oxidation product nopinone was detected in the aerosol and could be shown to decrease from 2 % of the total aerosol to 0.5 % of the aerosol over the 48 hours of

  7. Modeling the Relationships Between Aerosol Properties and the Direct and Indirect Effects of Aerosols on Climate

    NASA Technical Reports Server (NTRS)

    Toon, Owen B.

    1994-01-01

    Aerosols may affect climate directly by scattering and absorbing visible and infrared energy, They may also affect climate indirectly by modifying the properties of clouds through microphysical processes, and by altering abundances of radiatively important gases through heterogeneous chemistry. Researchers understand which aerosol properties control the direct effect of aerosols on the radiation budget. Unfortunately, despite an abundance of data on certain types of aerosols, much work remains to be done to determine the values of these properties. For instance we have little idea about the global distribution, seasonal variation, or interannual variability of the aerosol optical depth. Also we do not know the visible light absorption properties of tropical aerosols which may contain much debris from slash and burn agriculture. A positive correlation between aerosol concentrations and albedos of marine stratus clouds is observed, and the causative microphysics is understood. However, models suggest that it is difficult to produce new particles in the marine boundary layer. Some modelers have suggested that the particles in the marine boundary layer may originate in the free troposphere and be transported into the boundary layer. Others argue that the aerosols are created in the marine boundary layer. There are no data linking aerosol concentration and cirrus cloud albedo, and models suggest cirrus properties may not be very sensitive to aerosol abundance. There is clear evidence of a radiatively significant change in the global lower stratospheric ozone abundance during the past few decades. These changes are caused by heterogeneous chemical reactions occurring on the surfaces of particles. The rates of these reactions depend upon the chemical composition of the particles. Although rapid advances in understanding heterogeneous chemistry have been made, much remains to be done.

  8. Retrieving the Vertical Structure of the Effective Aerosol Complex Index of Refraction from a Combination of Aerosol in Situ and Remote Sensing Measurements During TARFOX

    NASA Technical Reports Server (NTRS)

    Redemann, J.; Turco, R. P.; Liou, K. N.; Russell, P. B.; Bergstrom, R. W.; Schmid, B.; Livingston, J. M.; Hobbs, P. V.; Hartley, W. S.; Ismail, S.

    2000-01-01

    The largest uncertainty in estimates of the effects of atmospheric aerosols on climate stems from uncertainties in the determination of their microphysical properties, including the aerosol complex index of refraction, which in turn determines their optical properties. A novel technique is used to estimate the aerosol complex index of refraction in distinct vertical layers from a combination of aerosol in situ size distribution and remote sensing measurements during the Tropospheric Aerosol Radiative Forcing Observational Experiment (TARFOX). In particular, aerosol backscatter measurements using the NASA Langley LASE (Lidar Atmospheric Sensing Experiment) instrument and in situ aerosol size distribution data are utilized to derive vertical profiles of the 'effective' aerosol complex index of refraction at 815 nm (i.e., the refractive index that would provide the same backscatter signal in a forward calculation on the basis of the measured in situ particle size distributions for homogeneous, spherical aerosols). A sensitivity study shows that this method yields small errors in the retrieved aerosol refractive indices, provided the errors in the lidar derived aerosol backscatter are less than 30% and random in nature. Absolute errors in the estimated aerosol refractive indices are generally less than 0.04 for the real part and can be as much as 0.042 for the imaginary part in the case of a 30% error in the lidar-derived aerosol backscatter. The measurements of aerosol optical depth from the NASA Ames Airborne Tracking Sunphotometer (AATS-6) are successfully incorporated into the new technique and help constrain the retrieved aerosol refractive indices. An application of the technique to two TARFOX case studies yields the occurrence of vertical layers of distinct aerosol refractive indices. Values of the estimated complex aerosol refractive index range from 1.33 to 1.45 for the real part and 0.001 to 0.008 for the imaginary part. The methodology devised in this study

  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. Validation of Retrieved Aerosol Optical Properties over Northeast Asia for Five Years from GOSAT TANSO-Cloud and Aerosol Imager

    NASA Astrophysics Data System (ADS)

    Kim, J.; Lee, S.; KIM, M.; Choi, M.; Go, S.; Lim, H.; Goo, T. Y.; Nakajima, T.; Kuze, A.; Shiomi, K.; Yokota, T.

    2015-12-01

    An aerosol retrieval algorithm was developed from Thermal And Near infrared Sensor for carbon Observation-Cloud and Aerosol Imager (TANSO-CAI) onboard the Greenhouse Gases Observing Satellite (GOSAT). The algorithm retrieves aerosol optical depth (AOD), size distribution of aerosol, and aerosol type in 0.1 degree grid resolution by look-up tables, which is used in retrieving optical properties of aerosol using inversion products from Aerosol Robotic NETwork (AERONET) sun-photometer observation. To improve the accuracy of aerosol algorithm, first, this algorithm considered the annually estimated radiometric degradation factor of TANSO-CAI suggested by Kuze et al. (2014). Second, surface reflectance was determined by two methods: one using the clear sky composite method from CAI measurements and the other the database from MODerate resolution Imaging Sensor (MODIS) surface reflectance data. At a given pixel, the surface reflectance is selected by using normalized difference vegetation index (NDVI) depending on season (Hsu et al., 2013). In this study, the retrieved AODs were compared with those of AERONET and MODIS dataset for different season over five years. Comparisons of AODs between AERONET and CAI show reasonable agreement with correlation coefficients of 0.65 ~ 0.97 and regression slopes between 0.7 and 1.2 for the whole period, depending on season and sites. Moreover, those between MODIS and CAI for the same period show agreements with correlation coefficients of 0.7 ~ 0.9 and regression slopes between 0.7 and 1.0, depending on season and regions. The results show reasonably good correlation, however, the largest error source in aerosol retrieval has been surface reflectance of TANSO-CAI due to its 3-days revisit orbit characteristics.

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

    NASA Astrophysics Data System (ADS)

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

    2008-02-01

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

  12. Ice Nucleation Properties of Amospherically Aged Biomass Burning Aerosol

    NASA Astrophysics Data System (ADS)

    Polen, M.; Lawlis, E.; Sullivan, R. C.

    2015-12-01

    Biomass burning can sometimes emit surprisingly active ice nucleating particles, though these emissions are not at all consistent between biomass fuel sources and burns. Soot from biomass combustion has been attributed to some but not all of the ice nucleating potential of biomass burning aerosol (BBA), while fossil fuel combustion soot emits very weak ice nucleants. The causes of the sometimes significant but variable ice nucleating ability of BBA are still largely unknown. BBA experiences significant atmospheric aging as the plume evolves and mixes with background air, yet almost no reports exploring the effects of atmospheric aging on the freezing properties of BBA have been made. We have performed some of the first experiments to determine the effects of simulated atmospheric aging on these ice nucleation properties, using a chamber reactor. The fresh and aged BBA was collected for subsequent droplet freezing array analysis using an impinger sampler to collect aerosol in water, and by deposition onto substrates in a MOUDI sampler. Droplets containing the chamber particles were then suspended in oil on a cold plate for freezing temperature spectrum measurement. Aging of Sawgrass flaming-phase combustion BBA by exposure to hydroxyl radicals (from H2O2 photolysis) enhanced the ice nucleation ability, observed by a shift to warmer droplet freezing temperatures by ~2-3°C. The changes in the aerosol's chemical composition during aging were observed using a laser ablation single-particle mass spectrometer and a soot-particle aerosol mass spectrometer. We will report our observations of the effects of other types of simulated aging (including photochemistry under high and low NOx conditions, dark ozonolysis, and nitric acid exposure) on Sawgrass and BBA from other grass and palm fuels.

  13. Hygroscopic, Morphological, and Chemical Properties of Agricultural Aerosols

    NASA Astrophysics Data System (ADS)

    Hiranuma, N.; Brooks, S. D.; Cheek, L.; Thornton, D. C.; Auvermann, B. W.; Littleton, R.

    2007-12-01

    Agricultural fugitive dust is a significant source of localized air pollution in the semi-arid southern Great Plains. In the Texas Panhandle, daily episodes of ground-level fugitive dust emissions from the cattle feedlots are routinely observed in conjunction with increased cattle activity in the late afternoons and early evenings. We conducted a field study to characterize size-selected agricultural aerosols with respect to hygroscopic, morphological, and chemical properties and to attempt to identify any correlations between these properties. To explore the hygroscopic nature of agricultural particles, we have collected size-resolved aerosol samples using a cascade impactor system at a cattle feedlot in the Texas Panhandle and have used the Environmental Scanning Electron Microscope (ESEM) to determine the water uptake by individual particles in those samples as a function of relative humidity. To characterize the size distribution of agricultural aerosols as a function of time, A GRIMM aerosol spectrometer and Sequential Mobility Particle Sizer and Counter (SMPS) measurements were simultaneously performed in an overall size range of 11 nm to 20 µm diameters at a cattle feedlot. Complementary determination of the elemental composition of individual particles was performed using Energy Dispersive X-ray Spectroscopy (EDS). In addition to the EDS analysis, an ammonia scrubber was used to collect ammonia and ammonium in the gas and particulate phases, respectively. The concentration of these species was quantified offline via UV spectrophotometry at 640 nanometers. The results of this study will provide important particulate emission data from a feedyard, needed to improve our understanding of the role of agricultural particulates in local and regional air quality.

  14. Characterization of Spectral Absorption Properties of Aerosols Using Satellite Observations

    NASA Technical Reports Server (NTRS)

    Torres, O.; Jethva, H.; Bhartia, P. K.; Ahn, C.

    2012-01-01

    The wavelength-dependence of aerosol absorption optical depth (AAOD) is generally represented in terms of the Angstrom Absorption Exponent (AAE), a parameter that describes the dependence of AAOD with wavelength. The AAE parameter is closely related to aerosol composition. Black carbon (BC) containing aerosols yield AAE values near unity whereas Organic carbon (OC) aerosol particles are associated with values larger than 2. Even larger AAE values have been reported for desert dust aerosol particles. Knowledge of spectral AAOD is necessary for the calculation of direct radiative forcing effect of aerosols and for inferring aerosol composition. We have developed a satellitebased method of determining the spectral AAOD of absorbing aerosols. The technique uses high spectral resolution measurements of upwelling radiation from scenes where absorbing aerosols lie above clouds as indicated by the UV Aerosol Index. For those conditions, the satellite measured reflectance (rho lambda) is approximately given by Beer's law rho lambda = rho (sub 0 lambda) e (exp -mtau (sub abs lambda)) where rho(sub 0 lambda) is the cloud reflectance, m is the geometric slant path and tau (sub abs lambda) is the spectral AAOD. The rho (sub 0 lambda) term is determined by means of radiative transfer calculations using as input the cloud optical depth derived as described in Torres et al. [JAS, 2012] that accounts for the effects of aerosol absorption. In the second step, corrections for molecular and aerosol scattering effects are applied to the cloud reflectance term, and the spectral AAOD is then derived by inverting the equation above. The proposed technique will be discussed in detail and application results will be presented. The technique can be easily applied to hyper-spectral satellite measurements that include UV such as OMI, GOME and SCIAMACHY, or to multi-spectral visible measurements by other sensors provided that the aerosol-above-cloud events are easily identified.

  15. Biogenic Aerosols Over the Amazon Basin: Optical Properties and Relationship With Elemental and Ionic Composition

    NASA Astrophysics Data System (ADS)

    Artaxo, P.; Martin, S. T.; Andreae, M. O.; Godoy, J. M.; Godoy, M. L.; Rizzo, L. V.; Paixao, M.

    2008-12-01

    We investigated the optical properties of natural biogenic aerosol particles over the central Amazon Basin near Manaus during the wet season in February and March 2008. The measurements were conducted as part of the AMAZE-08 (Amazonian Aerosol Characterization Experiment) sampling campaign. Light absorption was determined with the use of an Aethalometer and an MAAP (Multi Angle Absorption Photometer). Light scattering was measured with a 3 wavelength TSI nephelometer and an Ecotech nephelometer. The elemental composition was measured trough PIXE and IC. Single scattering albedo shows relatively low values varying from 0.86 to 0.95. Very low fine mode aerosol mass was measured, and coarse mode particles are responsible for a significant fraction of scattering and absorption. Sulfur was observed in very low concentrations, and most of the aerosol mass was organic. Long range transport of soil dust from Sahara were observed and reflected in the light scattering coefficient. Wavelength dependence of absorption indicates the strong influence of coarse mode aerosol. Aerosol optical thickness shows low values, but with significant single scattering albedo values, showing strong absorption properties of these biogenic aerosols. Size distribution measurements shows consistence with the scattering coefficients measured, if the coarse mode particles are taken into account.

  16. 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

  17. Polar Nephelometer Measurements of Aerosol Phase Functions: Calibration and Field Measurements in Hawaii and the UAE

    NASA Astrophysics Data System (ADS)

    Porter, J. N.

    2005-12-01

    A custom polar nephelometer was built to make open air aerosol phase function measurements. The system is calibrated using filtered air as well as known aerosols. Measurements of aerosol phase functions were made in Hawaii and the United Arab Emirates. Using Mie and Pollack and Cuzzi code, aerosol size distributions are inverted. Time permiting these results will be compared with aerosol size distribution measurements obtained by other techniques.

  18. Evidence for Natural Variability in Marine Stratocumulus Cloud Properties Due to Cloud-Aerosol

    NASA Technical Reports Server (NTRS)

    Albrecht, Bruce; Sharon, Tarah; Jonsson, Haf; Minnis, Patrick; Minnis, Patrick; Ayers, J. Kirk; Khaiyer, Mandana M.

    2004-01-01

    In this study, aircraft observations from the Interdisciplinary Remotely-Piloted Aircraft Studies (CIRPAS) Twin Otter are used to characterize the variability in drizzle, cloud, and aerosol properties associated with cloud rifts and the surrounding solid clouds observed off the coast of California. A flight made on 16 July 1999 provided measurements directly across an interface between solid and rift cloud conditions. Aircraft instrumentation allowed for measurements of aerosol, cloud droplet, and drizzle spectra. CCN concentrations were measured in addition to standard thermodynamic variables and the winds. A Forward Scatter Spectrometer Probe (FSSP) measured size distribution of cloud-sized droplets. A Cloud Imaging Probe (CIP) was used to measure distributions of drizzle-sized droplets. Aerosol distributions were obtained from a Cloud Aerosol Scatterprobe (CAS). The CAS probe measured aerosols, cloud droplets and drizzle-sized drops; for this study. The CAS probe was used to measure aerosols in the size range of 0.5 micron - 1 micron. Smaller aerosols were characterized using an Ultrafine Condensation Particle Counter (CPC) sensor. The CPC was used to measure particles with diameters greater than 0.003 micron. By subtracting different count concentrations measured with the CPC, this probe was capable of identifying ultrafine particles those falling in the size range of 3 nanometers - 7 nanometers that are believed to be associated with new particle production.

  19. Wavelength dependence of aerosol backscatter coefficients obtained by multiple wavelength Lidar measurements

    NASA Technical Reports Server (NTRS)

    Sasano, Y.; Browell, E. V.

    1986-01-01

    Aerosols are often classified into several general types according to their origins and composition, such as maritime, continental, and stratospheric aerosols, and these aerosol types generally have different characteristics in chemical and physical properties. The present study aims at demonstrating the potential for distinguishing these aerosol types by the wavelength dependence of their backscatter coefficients obtained from quantitative analyses of multiple wavelength lidar signals. Data from the NASA Airborne Differential Abosrption lidar (DIAL) S ystems, which can measure aerosol backscatter profiles at wavelenghts of 300, 600, and 1064 nm and ozone profiles of backscatter coefficients for these three wavelength were derived from the observations of aerosols of different types. Observations were performed over the Atlantic Ocean, the Southwestern United States, and French Guyana.

  20. Drop size measurement of liquid aerosols

    NASA Astrophysics Data System (ADS)

    Liu, B. Y. H.; Pui, D. Y. H.; Xian-Qing, Wang

    The factor B = D/ D' relating the diameter D of a spherical liquid drop to the diameter, D˜, of the same drop collected on a microscope slide has been measured for DOP (di-octyl phthalate) and oleic acid aerosols. The microscope slide was coated with a fluorocarbon, oleophobic surfactant (L-1428, 3M Co., St. Paul, MN). The ratio was found to be independent of drop diameter in the 2-50 μm range and the mean value of B was found to be 0.700 for oleic acid and 0.690 for DOP. Similar measurements for oleic acid and DOP drops collected on a clean, uncoated slide resulted in the values of 0.419 and 0.303, respectively. The experimental values of B were compared with the theoretical values based on contact angle measurements. Good agreement was obtained.

  1. Meteorological and aerosol effects on marine cloud microphysical properties

    NASA Astrophysics Data System (ADS)

    Sanchez, K. J.; Russell, L. M.; Modini, R. L.; Frossard, A. A.; Ahlm, L.; Corrigan, C. E.; Roberts, G. C.; Hawkins, L. N.; Schroder, J. C.; Bertram, A. K.; Zhao, R.; Lee, A. K. Y.; Lin, J. J.; Nenes, A.; Wang, Z.; Wonaschütz, A.; Sorooshian, A.; Noone, K. J.; Jonsson, H.; Toom, D.; Macdonald, A. M.; Leaitch, W. R.; Seinfeld, J. H.

    2016-04-01

    Meteorology and microphysics affect cloud formation, cloud droplet distributions, and shortwave reflectance. The Eastern Pacific Emitted Aerosol Cloud Experiment and the Stratocumulus Observations of Los-Angeles Emissions Derived Aerosol-Droplets studies provided measurements in six case studies of cloud thermodynamic properties, initial particle number distribution and composition, and cloud drop distribution. In this study, we use simulations from a chemical and microphysical aerosol-cloud parcel (ACP) model with explicit kinetic drop activation to reproduce observed cloud droplet distributions of the case studies. Four cases had subadiabatic lapse rates, resulting in fewer activated droplets, lower liquid water content, and higher cloud base height than an adiabatic lapse rate. A weighted ensemble of simulations that reflect measured variation in updraft velocity and cloud base height was used to reproduce observed droplet distributions. Simulations show that organic hygroscopicity in internally mixed cases causes small effects on cloud reflectivity (CR) (<0.01), except for cargo ship and smoke plumes, which increased CR by 0.02 and 0.07, respectively, owing to their high organic mass fraction. Organic hygroscopicity had larger effects on droplet concentrations for cases with higher aerosol concentrations near the critical diameter (namely, polluted cases with a modal peak near 0.1 µm). Differences in simulated droplet spectral widths (k) caused larger differences in CR than organic hygroscopicity in cases with organic mass fractions of 60% or less for the cases shown. Finally, simulations from a numerical parameterization of cloud droplet activation suitable for general circulation models compared well with the ACP model, except under high organic mass fraction.

  2. The chemical evolution & physical properties of organic aerosol: A molecular structure based approach

    NASA Astrophysics Data System (ADS)

    Wei, Yiyi; Cao, Tingting; Thompson, Jonathan E.

    2012-12-01

    Global climate, atmospheric chemistry, and air quality are affected by tropospheric particulate matter. Recent measurements suggest organic compounds present in this haze comprise roughly half of total aerosol fine mass concentration globally. Unlike the well-constrained processes which result in formation of nitrate or sulfate aerosol, the oxidation of volatile organics in the atmosphere can lead to thousands of stable compounds in the aerosol phase. Development of a tractable framework to consider the chemical and physical evolution of the organic aerosol is crucial for modeling its effect on global climate. Here we show coupling a 3-dimensional coordinate system defined by the molecular descriptors of molecular weight, heteroatom mass, and double bond equivalents (D.B.E.) with high-resolution molecular mass spectrometry is a powerful approach for describing key properties of the organic aerosol. The scheme is conceptually simple, yet maintains sufficient complexity to be compatible with quantitative structure-property relationships (QSPRs) used to predict chemical and physical properties that govern aerosol behavior. From available data, both ambient organic aerosol and laboratory generated organic aerosol frequently occupy the region characterized by <10 D.B.E. <600 M.W. and <200 heteroatom mass. A QSPR analysis conducted illustrates spatial trends within the 3D space for volatility and Henry's law constants for 31,000 organic compounds considered.

  3. Aerosol absorption measurement at SWIR with water vapor interference using a differential photoacoustic spectrometer.

    PubMed

    Zhu, Wenyue; Liu, Qiang; Wu, Yi

    2015-09-01

    Atmospheric aerosol plays an important role in atmospheric radiation balance through absorbing and scattering the solar radiation, which changes local weather and global climate. Accurate measurement is highly requested to estimate the radiative effects and climate effects of atmospheric aerosol. Photoacoustic spectroscopy (PAS) technique, which observes the aerosols on their natural suspended state and is insensitive to light scattering, is commonly recognized as one of the best candidates to measure the optical absorption coefficient (OAC) of aerosols. In the present work, a method of measuring aerosol OAC at the wavelength where could also be absorbed by water vapor was proposed and corresponding measurements of the absorption properties of the atmospheric aerosol at the short wave infrared (SWIR, 1342 nm) wavelength were carried out. The spectrometer was made up of two high performance homemade photoacoustic cells. To improve the sensitivity, several methods were presented to control the noise derived from gas flow and vibration from the sampling pump. Calibration of the OAC and properties of the system were also studied in detail. Using the established PAS instrument, measurement of the optical absorption properties of the atmospheric aerosol were carried out in laboratory and field environment.

  4. Aerosol absorption measurement at SWIR with water vapor interference using a differential photoacoustic spectrometer.

    PubMed

    Zhu, Wenyue; Liu, Qiang; Wu, Yi

    2015-09-01

    Atmospheric aerosol plays an important role in atmospheric radiation balance through absorbing and scattering the solar radiation, which changes local weather and global climate. Accurate measurement is highly requested to estimate the radiative effects and climate effects of atmospheric aerosol. Photoacoustic spectroscopy (PAS) technique, which observes the aerosols on their natural suspended state and is insensitive to light scattering, is commonly recognized as one of the best candidates to measure the optical absorption coefficient (OAC) of aerosols. In the present work, a method of measuring aerosol OAC at the wavelength where could also be absorbed by water vapor was proposed and corresponding measurements of the absorption properties of the atmospheric aerosol at the short wave infrared (SWIR, 1342 nm) wavelength were carried out. The spectrometer was made up of two high performance homemade photoacoustic cells. To improve the sensitivity, several methods were presented to control the noise derived from gas flow and vibration from the sampling pump. Calibration of the OAC and properties of the system were also studied in detail. Using the established PAS instrument, measurement of the optical absorption properties of the atmospheric aerosol were carried out in laboratory and field environment. PMID:26368414

  5. Quantifying aerosol mixing state with entropy and diversity measures

    NASA Astrophysics Data System (ADS)

    Riemer, N.; West, M.

    2013-11-01

    This paper presents the first quantitative metric for aerosol population mixing state, defined as the distribution of per-particle chemical species composition. This new metric, the mixing state index χ, is an affine ratio of the average per-particle species diversity Dα and the bulk population species diversity Dγ, both of which are based on information-theoretic entropy measures. The mixing state index χ enables the first rigorous definition of the spectrum of mixing states from so-called external mixture to internal mixture, which is significant for aerosol climate impacts, including aerosol optical properties and cloud condensation nuclei activity. We illustrate the usefulness of this new mixing state framework with model results from the stochastic particle-resolved model PartMC-MOSAIC. These results demonstrate how the mixing state metrics evolve with time for several archetypal cases, each of which isolates a specific process such as coagulation, emission, or condensation. Further, we present an analysis of the mixing state evolution for a complex urban plume case, for which these processes occur simultaneously. We additionally derive theoretical properties of the mixing state index and present a family of generalized mixing state indexes that vary in the importance assigned to low-mass-fraction species.

  6. Case study of modeled aerosol optical properties during the SAFARI 2000 campaign.

    PubMed

    Kuzmanoski, Maja; Box, Michael A; Schmid, Beat; Russell, Philip B; Redemann, Jens

    2007-08-01

    We present modeled aerosol optical properties (single scattering albedo, asymmetry parameter, and lidar ratio) in two layers with different aerosol loadings and particle sizes, observed during the Southern African Regional Science Initiative 2,000 (SAFARI 2,000) campaign. The optical properties were calculated from aerosol size distributions retrieved from aerosol layer optical thickness spectra, measured using the NASA Ames airborne tracking 14-channel sunphotometer (AATS-14) and the refractive index based on the available information on aerosol chemical composition. The study focuses on sensitivity of modeled optical properties in the 0.3-1.5 microm wavelength range to assumptions regarding the mixing scenario. We considered two models for the mixture of absorbing and nonabsorbing aerosol components commonly used to model optical properties of biomass burning aerosol: a layered sphere with absorbing core and nonabsorbing shell and the Maxwell-Garnett effective medium model. In addition, comparisons of modeled optical properties with the measurements are discussed. We also estimated the radiative effect of the difference in aerosol absorption implied by the large difference between the single scattering albedo values (approximately 0.1 at midvisible wavelengths) obtained from different measurement methods for the case with a high amount of biomass burning particles. For that purpose, the volume fraction of black carbon was varied to obtain a range of single scattering albedo values (0.81-0.91 at lambda=0.50 microm). The difference in absorption resulted in a significant difference in the instantaneous radiative forcing at the surface and the top of the atmosphere (TOA) and can result in a change of the sign of the aerosol forcing at TOA from negative to positive.

  7. Aerosol Retrieval from Multiangle Multispectral Photopolarimetric Measurements: Importance of Spectral Range and Angular Resolution

    NASA Technical Reports Server (NTRS)

    Wu, L.; Hasekamp, O.; Van Diedenhoven, B.; Cairns, B.

    2015-01-01

    We investigated the importance of spectral range and angular resolution for aerosol retrieval from multiangle photopolarimetric measurements over land. For this purpose, we use an extensive set of simulated measurements for different spectral ranges and angular resolutions and subsets of real measurements of the airborne Research Scanning Polarimeter (RSP) carried out during the PODEX and SEAC4RS campaigns over the continental USA. Aerosol retrievals performed from RSP measurements show good agreement with ground-based AERONET measurements for aerosol optical depth (AOD), single scattering albedo (SSA) and refractive index. Furthermore, we found that inclusion of shortwave infrared bands (1590 and/or 2250 nm) significantly improves the retrieval of AOD, SSA and coarse mode microphysical properties. However, accuracies of the retrieved aerosol properties do not improve significantly when more than five viewing angles are used in the retrieval.

  8. Cloud Nucleating Properties of Aerosols During TexAQS - GoMACCS 2006: Influence of Aerosol Sources, Composition, and Size

    NASA Astrophysics Data System (ADS)

    Quinn, P. K.; Bates, T. S.; Coffman, D. J.; Covert, D. S.; Onasch, T. B.; Alllan, J. D.; Worsnop, D.

    2006-12-01

    TexAQS - GoMACCS 2006 was conducted from July to September 2006 in the Gulf of Mexico and Houston Ship Channel to investigate sources and processing of gas and particulate phase species and to determine their impact on regional air quality and climate. As part of the experiment, the NOAA R.V. Ronald H. Brown transited from Charleston, S.C. to the study region. The ship was equipped with a full compliment of gas and aerosol instruments. To determine the cloud nucleating properties of aerosols, measurements were made of the aerosol number size distribution, aerosol chemical composition, and cloud condensation nuclei (CCN) concentration at five supersaturations. During the transit and over the course of the experiment, a wide range of aerosol sources and types was encountered. These included urban and industrial emissions from the S.E. U.S. as the ship left Charleston, a mixture of Saharan dust and marine aerosol during the transit around Florida and across the Gulf of Mexico, urban emissions from Houston, and emissions from the petrochemical industries, oil platforms, and marine vessels in the Gulf coast region. Highest activation ratios (ratio of CCN to total particle number concentration at 0.4 percent supersaturation) were measured in anthropogenic air masses when the aerosol was composed primarily of ammonium sulfate salts and in marine air masses with an aerosol composed of sulfate and sea salt. A strong gradient in activation ratio was measured as the ship moved from the Gulf of Mexico to the end of the Houston Ship Channel (values decreasing from about 0.8 to less than 0.1) and the aerosol changed from marine to industrial. The activation ratio under these different regimes in addition to downwind of marine vessels and oil platforms will be discussed in the context of the aerosol size distribution and chemical composition. The discussion of composition will include the organic mass fraction of the aerosol, the degree of oxidation of the organics, and the water

  9. Quantification of black carbon mixing state from traffic: implications for aerosol optical properties

    NASA Astrophysics Data System (ADS)

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

    2016-04-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2015-11-01

    The climatic impacts of black carbon (BC) aerosol, an important absorber of solar radiation in the atmosphere, remain poorly constrained and are intimately related to its particle-scale physical and chemical properties. Using particle-resolved modelling informed by quantitative measurements from a soot-particle aerosol mass spectrometer, we confirm that the mixing state (the distribution of co-emitted aerosol amongst fresh BC-containing particles) at the time of emission significantly affects BC-aerosol optical properties even after a day of atmospheric processing. Both single particle and ensemble aerosol mass spectrometry observations indicate that BC near the point of emission co-exists with hydrocarbon-like organic aerosol in two distinct particle types: HOA-rich and BC-rich particles. The average mass fraction of black carbon in HOA-rich and BC-rich particles was 0.02-0.08 and 0.72-0.93, respectively. Notably, approximately 90 % of BC mass resides in BC-rich particles. This new measurement capability provides quantitative insight into the physical and chemical nature of BC-containing particles and is used to drive a particle-resolved aerosol box model. Significant differences in calculated single scattering albedo (an increase of 0.1) arise from accurate treatment of initial particle mixing state as compared to the assumption of uniform aerosol composition at the point of BC injection into the atmosphere.

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

    DOE PAGES

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

    2016-04-14

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

  12. Simultaneous In-Situ Measurement of Local Particle Size, Particle Concentration, and Velocity of Aerosols.

    PubMed

    Weber; Schweiger

    1999-02-01

    Photon correlation spectroscopy has been applied to the characterization of (quasi-)monodisperse aerosols. The experiments were carried out with an experimental standard pin hole setup on laminar flowing aerosols of the submicrometer particle size range. It is shown that beside local mean particle size and local aerosol velocity simultaneously the local particle number concentration may be obtained from a single measured autocorrelation function. The proposed procedure does not require calibration. It is pointed out that measurement conditions can be adapted to the properties of the aerosol to be characterized, thus allowing characterization of aerosols over a wide parameter range, e.g., it is not restricted to the case of low particle concentration. The experimental results are compared to data from literature, data from reference measurements and data from a theoretical model, respectively. The method can also be usefull for characterization of other fluid-particle systems as hydrosols. Copyright 1999 Academic Press.

  13. Uncertainties of simulated aerosol optical properties induced by assumptions on aerosol physical and chemical properties: an AQMEII-2 perspective

    EPA Science Inventory

    The calculation of aerosol optical properties from aerosol mass is a process subject to uncertainty related to necessary assumptions on the treatment of the chemical species mixing state, density, refractive index, and hygroscopic growth. In the framework of the AQMEII-2 model in...

  14. Satellite and in-situ derived aerosol optical properties over the TCAP campaign region

    NASA Astrophysics Data System (ADS)

    Chand, D.; Berg, L. K.; Ferrare, R. A.; Barnard, J.; Berkowitz, C. M.; Chapman, E.; Comstock, J. M.; Fast, J. D.; Flynn, C. J.; Hair, J. W.; Hostetler, C. A.; Hubbe, J.; Kassianov, E.; Kluzek, C. D.; Pekour, M. S.; Sedlacek, A. J.; Schmid, B.; Shilling, J. E.; Shinozuka, Y.; Tomlinson, J. M.; Wilson, J. M.; Zelenyuk, A.

    2012-12-01

    The direct radiative effect of natural and anthropogenic aerosol is one of the largest uncertainties in the prediction of climate change at regional and global scales. The uncertainties in atmospheric radiative forcing are in part a result of limited knowledge of aerosol optical properties. In this presentation we discuss in-situ and satellite derived aerosol optical properties obtained within the Two-Column Aerosol Project (TCAP) campaign region, and explore their links with aerosol chemical and physical properties. The TCAP field campaign is designed to provide observations of the size distribution, chemical properties, and optical properties of aerosol within and between two atmospheric columns along the eastern seaboard of the United States. These columns are separated by 200-300 km and were sampled in July 2012 during a summer intensive operation period (IOP) using the U.S. Department of Energy's Gulfstream-1 (G-1) and NASA's B200 aircraft and the surface-based DOE Atmospheric Radiation Measurement (ARM) Mobile Facility (AMF) located at Cape Cod. In contrast to the aircraft IOP, the AMF will be operated continuously until the summer of 2013.The surface observations will test the veracity of cloud and radiative transfer models over a wider range of conditions than can be observed via the short-term aircraft IOPs. In this presentation we will examine the spectral dependence of the aerosol optical properties with a focus on in-situ as well as remote sensing observations during the summer (July) over the TCAP region. We will also use multiple years of observations from MODIS, CALIPSO, and OMI satellite sensors and develop the climatology of aerosol optical depth (AOD), single scattering albedo (SSA) and aerosol layer altitudes to put the TCAP observations into a larger perspective. In addition, in-situ observations of light scattering and absorption coefficients made using the G-1, and AOD and aerosol features derived from the NASA High Spectral Resolution Lidar

  15. Physico-chemical properties of aerosols in Sao Paulo, Brazil and mechanisms of secondary organic aerosol formation.

    NASA Astrophysics Data System (ADS)

    Artaxo, Paulo; Ferreira de Brito, Joel; Varanda Rizzo, Luciana; Luiza Godoy, Maria; Godoy, Jose Marcus

    2013-04-01

    Megacities emissions are increasingly becoming a global issue, where emissions from the transportation sector play an increasingly important role. Sao Paulo is a megacity with a population of about 18 million people, 7 million cars and large-scale industrial emissions. As a result of the vehicular and industrial emissions, the air quality in Sao Paulo is bellow WMO standards for aerosol particles and ozone. Many uncertainties are found on gas- and particulate matter vehicular emission factors and their following atmospheric processes, e.g. secondary organic aerosol formation. Due to the uniqueness of the vehicular fuel in Brazil, largely based on ethanol use, such characterization currently holds further uncertainties. To improve the understanding of the role of this unique emission characteristics, we are running a source apportionment study in Sao Paulo focused on the mechanisms of organic aerosol formation. One of the goals of this study is a quantitative aerosol source apportionment focused on vehicular emissions, including ethanol and gasohol (both fuels used by light-duty vehicles). This study comprises four sampling sites with continuous measurements for one year, where trace elements and organic aerosol are being measured for PM2.5 and PM10 along with real-time NOx, O3, PM10 and CO measurements. Aerosol optical properties and size distribution are being measured on a rotation basis between sampling stations. Furthermore, a Proton-Transfer-Reaction Mass Spectrometer (PTR-MS) and an Aerosol Chemical Speciation Monitor (ACSM) are used to measure in real time VOCs and aerosol composition, respectively. Trace elements were measured using XRF and OC/EC analysis was determined with a Sunset OC/EC instrument. A TSI Nephelometer with 3 wavelengths measure light scattering and a MAAP measure black carbon. Results show aerosol number concentrations ranging between 10,000 and 35,000 cm-3, mostly concentrated in the nucleation and Aitken modes, with a peak in size at 80

  16. Systematic Relationships among Background SE U.S. Aerosol Optical, Micro-physical, and Chemical Properties-Development of an Optically-based Aerosol Characterization

    NASA Astrophysics Data System (ADS)

    Sherman, J. P.; Link, M. F.; Zhou, Y.

    2014-12-01

    Remote sensing-based retrievals of aerosol composition require known or assumed relationships between aerosol optical properties and types. Most optically-based aerosol classification schemes apply some combination of the spectral dependence of aerosol light scattering and absorption-using the absorption and either scattering or extinction Angstrom exponents (AAE, SAE and EAE), along with single-scattering albedo (SSA). These schemes can differentiate between such aerosol types as dust, biomass burning, and urban/industrial but no such studies have been conducted in the SE U.S., where a large fraction of the background aerosol is a variable mixture of biogenic SOA, sulfates, and black carbon. In addition, AERONET retrievals of SSA are often highly uncertain due to low AOD in the region during most months. The high-elevation, semi-rural AppalAIR facility at Appalachian State University in Boone, NC (1090m ASL, 36.210N, 81.690W) is home to the only co-located NOAA-ESRL and AERONET monitoring sites in the eastern U.S. Aerosol chemistry measured at AppalAIR is representative of the background SE U.S (Link et al. 2014) Dried aerosol light absorption and dried and humidified aerosol light scattering and hemispheric backscattering at 3 visible wavelengths and 2 particle size cuts (sub-1μm and sub-10μm) are measured continuously. Measurements of size-resolved, non-refractory sub-1μm aerosol composition were made by a co-located AMS during the 2012-2013 summers and 2013 winter. Systematic relationships among aerosol optical, microphysical, and chemical properties were developed to better understand aerosol sources and processes and for use in higher-dimension aerosol classification schemes. The hygroscopic dependence of visible light scattering is sensitive to the ratio of sulfate to organic aerosol(OA), as are SSA and AAE. SAE is a less sensitive indicator of fine-mode aerosol size than hemispheric backscatter fraction (b) and is more sensitive to fine-mode aerosol

  17. Aerosol and CCN properties at Princess Elisabeth station, East Antarctica: seasonality, new particle formation events and properties around precipitation events

    NASA Astrophysics Data System (ADS)

    Mangold, Alexander; Laffineur, Quentin; De Backer, Hugo; Herenz, Paul; Wex, Heike; Gossart, Alexandra; Souverijns, Niels; Gorodetskaya, Irina; Van Lipzig, Nicole

    2016-04-01

    Since 2010, several complementary ground-based instruments for measuring the aerosol composition of the Antarctic atmosphere have been operated at the Belgian Antarctic research station Princess Elisabeth, in Dronning Maud Land, East Antarctica (71.95° S, 23.35° E, 1390 m asl.). In addition, three ground-based remote sensing instruments for cloud and precipitation observations have been installed for continuous operation, including a ceilometer (cloud base height, type, vertical extent), a 24 Ghz micro-rain radar (vertical profiles of radar effective reflectivity and Doppler velocity), and a pyrometer (cloud base temperature). The station is inhabited from November to end of February and operates under remote control during the other months. In this contribution, the general aerosol and cloud condensation nuclei (CCN) properties will be described with a special focus on new particle formation events and around precipitation events. New particle formation events are important for the atmospheric aerosol budget and they also show that aerosols are not only transported to Antarctica but are also produced there, also inland. Aerosols are essential for cloud formation and therefore also for precipitation, which is the only source for mass gain of the Antarctic ice sheet. Measured aerosol properties comprise size distribution, total number, total mass concentration, mass concentration of light-absorbing aerosol and absorption coefficient and total scattering coefficient. In addition, a CCN counter has been operated during austral summers 2013/14, 2014/15 and 2015/16. The baseline total number concentration N-total was around some hundreds of particles/cm3. During new particle formation events N-total increased to some thousands of particles/cm3. Simultaneous measurements of N-total, size distribution and CCN number revealed that mostly the number of particles smaller than 100 nm increased and that the concentration of cloud condensation nuclei increased only very

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

    SciTech Connect

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

    2013-11-01

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

  19. Retrieval of Aerosol Absorption Properties from Satellite Observations

    NASA Technical Reports Server (NTRS)

    Torres, Omar; Bhartia, Pawan K.; Jethva, H.; Ahn, Chang-Woo

    2012-01-01

    The Angstrom Absorption Exponent (AAE) is a parameter commonly used to characterize the wavelength-dependence of aerosol absorption optical depth (AAOD). It is closely related to aerosol composition. Black carbon (BC) containing aerosols yield AAE values near unity whereas Organic carbon (OC) aerosol particles are associated with values larger than 2. Even larger AAE values have been reported for desert dust aerosol particles. Knowledge of spectral AAOD is necessary for the calculation of direct radiative forcing effect of aerosols and for inferring aerosol composition. We have developed a satellitebased method of determining the spectral AAOD of absorbing aerosols. The technique uses multi-spectral measurements of upwelling radiation from scenes where absorbing aerosols lie above clouds as indicated by the UV Aerosol Index. For those conditions, the satellite measurement can be explained, using an approximations of Beer's Law (BL), as the upwelling reflectance at the cloud top attenuated by the absorption effects of the overlying aerosol layer. The upwelling reflectance at the cloud-top in an aerosol-free atmospheric column is mainly a function of cloud optical depth (COD). In the proposed method of AAE derivation, the first step is determining COD which is retrieved using a previously developed color-ratio based approach. In the second step, corrections for molecular scattering effects are applied to both the observed ad the calculated cloud reflectance terms, and the spectral AAOD is then derived by an inversion of the BL approximation. The proposed technique will be discussed in detail and application results making use of OMI multi-spectral measurements in the UV-Vis. will be presented.

  20. New Measurements of Aerosol Vertical Structure from Space using the NASA Geoscience Laser Altimeter System (GLAS): Applications for Aerosol Transport Models

    NASA Technical Reports Server (NTRS)

    Welton, E. J.; Spinhime, J.; Palm, S.; Hlavka, D.; Hart, W.; Ginoux, P.; Chin, M.; Colarco, P.

    2004-01-01

    In the past, satellite measurements of aerosols have only been possible using passive sensors. Analysis of passive satellite data has lead to an improved understanding of aerosol properties, spatial distribution, and their effect on the earth,s climate. However, direct measurement of aerosol vertical distribution has not been possible using only the passive data. Knowledge of aerosol vertical distribution is important to correctly assess the impact of aerosol absorption, for certain atmospheric correction procedures, and to help constrain height profiles in aerosol transport models. On January 12,2003 NASA launched the first satellite-based lidar, the Geoscience Laser Altimeter System (GLAS), onboard the ICESat spacecraft. GLAS is both an altimeter and an atmospheric lidar, and obtains direct measurements of aerosol and cloud heights. Here we show an overview of GLAS, provide an update of its current status, and discuss how GLAS data will be useful for modeling efforts. In particular, a strategy of using GLAS to characterize the height profile of dust plumes over source regions will be presented, along with initial results. Such information can be used to validate and improve output from aerosol transport models. Aerosol height profile comparisons between GLAS and transport models will be shown for regions downwind of aerosol sources. We will also discuss the feasibility of assimilating GLAS profiles into the models in order to improve their output.

  1. New Measurements of Aerosol Vertical Structure from Space Using the NASA Geoscience Laser Altimeter System (GLAS): Applications for Aerosol Transport Models

    NASA Technical Reports Server (NTRS)

    Welton, Ellsworth J.; Ginoux, Paul; Colarco, Peter; Chin, Mian; Spinhirne, James D.; Palm, Steven P.; Hlavka, Dennis; Hart, William

    2003-01-01

    In the past, satellite measurements of aerosols have only been possible using passive sensors. Analysis of passive satellite data has lead to an improved understanding of aerosol properties, spatial distribution, and their effect on the earth s climate. However, direct measurement of aerosol vertical distribution has not been possible using only the passive data. Knowledge of aerosol vertical distribution is important to correctly assess the impact of aerosol absorption, for certain atmospheric correction procedures, and to help constrain height profiles in aerosol transport models. On January 12,2003 NASA launched the first satellite-based lidar, the Geoscience Laser Altimeter System (GLAS), onboard the ICESat spacecraft. GLAS is both an altimeter and an atmospheric lidar, and obtains direct measurements of aerosol and cloud heights. Here we show an overview of GLAS, provide an update of its current status, and discuss how GUS data will be useful for modeling efforts. In particular, a strategy of using GLAS to characterize the height profile of dust plumes over source regions will be presented, along with initial results. Such information can be used to validate and improve output from aerosol transport models. Aerosol height profile comparisons between GLAS and transport models will be shown for regions downwind of aerosol sources. We will also discuss the feasibility of assimilating GLAS profiles into the models in order to improve their output,

  2. Retrieval of Aerosol information from UV measurement by using optimal estimation method

    NASA Astrophysics Data System (ADS)

    KIM, M.; Kim, J.; Jeong, U.; Kim, W. V.; Kim, S. K.; Lee, S. D.; Moon, K. J.

    2014-12-01

    An algorithm to retrieve aerosol optical depth (AOD), single scattering albedo (SSA), and aerosol loading height is developed for GEMS (Geostationary Environment Monitoring Spectrometer) measurement. The GEMS is planned to be launched in geostationary orbit in 2018, and employs hyper-spectral imaging with 0.6 nm resolution to observe solar backscatter radiation in the UV and Visible range. In the UV range, the low surface contribution to the backscattered radiation and strong interaction between aerosol absorption and molecular scattering can be advantageous in retrieving aerosol information such as AOD and SSA [Torres et al., 2007; Torres et al., 2013; Ahn et al., 2014]. However, the large contribution of atmospheric scattering results in the increase of the sensitivity of the backward radiance to aerosol loading height. Thus, the assumption of aerosol loading height becomes important issue to obtain accurate result. Accordingly, this study focused on the simultaneous retrieval of aerosol loading height with AOD and SSA by utilizing the optimal estimation method. For the RTM simulation, the aerosol optical properties were analyzed from AERONET inversion data (level 2.0) at 46 AERONET sites over ASIA. Also, 2-channel inversion method is applied to estimate a priori value of the aerosol information to solve the Lavenberg Marquardt equation. The GEMS aerosol algorithm is tested with OMI level-1B dataset, a provisional data for GEMS measurement, and the result is compared with OMI standard aerosol product and AERONET values. The retrieved AOD and SSA show reasonable distribution compared with OMI products, and are well correlated with the value measured from AERONET. However, retrieval uncertainty in aerosol loading height is relatively larger than other results.

  3. An AeroCom Initial Assessment - Optical Properties in Aerosol Component Modules of Global Models

    SciTech Connect

    Kinne, Stefan; Schulz, M.; Textor, C.; Guibert, S.; Balkanski, Y.; Bauer, S.; Berntsen, T.; Berglen, T.; Boucher, Olivier; Chin, M.; Collins, W.; Dentener, F.; Diehl, T.; Easter, Richard C.; Feichter, H.; Fillmore, D.; Ghan, Steven J.; Ginoux, P.; Gong, S.; Grini, A.; Hendricks, J.; Herzog, M.; Horrowitz, L.; Isaksen, I.; Iversen, T.; Kirkevag, A.; Kloster, S.; Koch, D.; Kristjansson, J. E.; Krol, M.; Lauer, A.; Lamarque, J. F.; Lesins, G.; Liu, Xiaohong; Lohmann, U.; Montanaro, V.; Myhre, G.; Penner, Joyce E.; Pitari, G.; Reddy, S.; Seland, O.; Stier, P.; Takemura, T.; Tie, X.

    2006-05-29

    The AeroCom exercise diagnoses multi-component aerosol modules in global modeling. In an initial assessment global fields for mass and for mid-visible aerosol optical thickness (aot) were compared among aerosol component modules of 21 different global models. There is general agreement among models for the annual global mean of component combined aot. At 0.12 to 0.14, simulated aot values are at the lower end of global averages suggested by remote sensing from ground (AERONET ca 0.14) and space (MODIS-MISR composite ca 0.16). More detailed comparisons, however, reveal that larger differences in regional distribution and significant differences in compositional mixture have remained. Of particular concern is the large model diversity for contributions by dust and carbon, because it leads to significant uncertainty in aerosol absorption (aab). Since not only aot but also aab influence the aerosol impact on the radiative energy-balance, aerosol (direct) forcing uncertainty in modeling is larger than differences in aot might suggest. New diagnostic approaches are proposed to trace model differences in terms of aerosol processing and transport: These include the prescription of common input (e.g. amount, size and injection of aerosol component emissions) and the use of observational capabilities from ground (e.g. measurements networks) and space (e.g. correlations between retrieved aerosol and cloud properties).

  4. Global volcanic aerosol properties derived from emissions, 1990-2015, using CESM1(WACCM)

    NASA Astrophysics Data System (ADS)

    Mills, Michael; Schmidt, Anja; Easter, Richard; Solomon, Susan; Kinnison, Douglas; Ghan, Steven; Neely, Ryan; Marsh, Daniel; Conley, Andrew; Bardeen, Charles; Gettelman, Andrew

    2016-04-01

    Accurate representation of global stratospheric aerosols from volcanic and non-volcanic sulfur emissions is key to understanding the cooling effects and ozone-losses that may be linked to volcanic activity. Attribution of climate variability to volcanic activity is of particular interest in relation to the post-2000 slowing in the rate of global average temperature increases. We have compiled a database of volcanic SO2 emissions and plume altitudes for eruptions from 1990 to 2015, and developed a new prognostic capability for simulating stratospheric sulfate aerosols in the Community Earth System Model (CESM). We combined these with other non-volcanic emissions of sulfur sources to reconstruct global aerosol properties from 1990 to 2015. Our calculations show remarkable agreement with ground-based lidar observations of stratospheric aerosol optical depth (SAOD), and with in situ measurements of stratospheric aerosol surface area density (SAD). These properties are key parameters in calculating the radiative and chemical effects of stratospheric aerosols. Our SAOD calculations represent a clear improvement over available satellite-based analyses, which generally ignore aerosol extinction below 15 km, a region that can contain the vast majority of stratospheric aerosol extinction at mid- and high-latitudes. Our SAD calculations greatly improve on that provided for the Chemistry-Climate Model Initiative, which misses about 60% of the SAD measured in situ on average during both volcanically active and volcanically quiescent periods. The stark differences in SAOD and SAD compared to other data sets will have significant effects on calculations of the radiative forcing of climate and global stratospheric chemistry over the period 2005-2015. In light of these results, the impact of volcanic aerosols in reducing the rate of global average temperature increases since the year 2000 should be revisited. We have made our calculated aerosol properties from January 1990 to

  5. Spatial variation of aerosol optical properties in North China Plain

    NASA Astrophysics Data System (ADS)

    Fan, Xuehua

    2013-04-01

    The column-integrated optical properties of aerosol in Beijing and Xianghe situated at North China Plain were investigated based on Sun/sky radiometer measurements made at Aerosol Robotic Network (AERONET) sites. Only version 2 and level 2 quality-assured data were presented and analyzed in this paper. Time intervals differ for the two sites, with Beijing having 9 years of data (Mar.-May, 2001; Apr., 2002-Dec., 2011),while Xianghe having 6 years of data (Mar.-Apr., 2001;Sep., 2004-Dec.,2011). Monthly mean 500 nm AOT values reach a maximum in June (0.95) and exceed 0.55 from March through September, and the minimum values occur during the late fall and winter months of November through February at Beijing. The monthly mean AOT values at Xianghe are very close to those measured at Beijing. The absolute differences of AOT between the two sites are less than 0.1 except in June and July. The reason of large difference in June and July is the frequently cloud contamination in summer result in the monthly means over the two sites computed from a large number of measurements of different date. The monthly averaged AOT with the same date in June and July are re-computed and the absolute difference of AOT between Beijing and Xianghe reduced to 0.01 and 0.03 in June and July respectively. The monthly mean Angstrom Exponent (AE) in Beijing and Xianghe sites are very close, with the absolute difference less than 0.075. The monthly mean AE in the two sites varied between ~1.0 and ~1.3 except in spring (March-May), therefore clearly dominated by fine mode aerosol for most of the year. All monthly averaged SSA at Beijing showed much lower value as compared to Xianghe though the seasonal variations are similar for the two sites, which indicates that aerosol absorption is greater in Beijing. All monthly averaged imaginary part of refractive index at Beijing has much higher value than Xianghe. The absolute differences of SSA between the two sites range from 0.016 to 0.037 except that

  6. Aerosol optical properties in the southeastern United States in summer - Part 2: Sensitivity of aerosol optical depth to relative humidity and aerosol parameters

    NASA Astrophysics Data System (ADS)

    Brock, Charles A.; Wagner, Nicholas L.; Anderson, Bruce E.; Beyersdorf, Andreas; Campuzano-Jost, Pedro; Day, Douglas A.; Diskin, Glenn S.; Gordon, Timothy D.; Jimenez, Jose L.; Lack, Daniel A.; Liao, Jin; Markovic, Milos Z.; Middlebrook, Ann M.; Perring, Anne E.; Richardson, Matthews S.; Schwarz, Joshua P.; Welti, Andre; Ziemba, Luke D.; Murphy, Daniel M.

    2016-04-01

    Aircraft observations of meteorological, trace gas, and aerosol properties were made between May and September 2013 in the southeastern United States (US). Regionally representative aggregate vertical profiles of median and interdecile ranges of the measured parameters were constructed from 37 individual aircraft profiles made in the afternoon when a well-mixed boundary layer with typical fair-weather cumulus was present (Wagner et al., 2015). We use these 0-4 km aggregate profiles and a simple model to calculate the sensitivity of aerosol optical depth (AOD) to changes in dry aerosol mass, relative humidity, mixed-layer height, the central diameter and width of the particle size distribution, hygroscopicity, and dry and wet refractive index, while holding the other parameters constant. The calculated sensitivity is a result of both the intrinsic sensitivity and the observed range of variation in these parameters. These observationally based sensitivity studies indicate that the relationship between AOD and dry aerosol mass in these conditions in the southeastern US can be highly variable and is especially sensitive to relative humidity (RH). For example, calculated AOD ranged from 0.137 to 0.305 as the RH was varied between the 10th and 90th percentile profiles with dry aerosol mass held constant. Calculated AOD was somewhat less sensitive to aerosol hygroscopicity, mean size, and geometric standard deviation, σg. However, some chemistry-climate models prescribe values of σg substantially larger than we or others observe, leading to potential high biases in model-calculated AOD of ˜ 25 %. Finally, AOD was least sensitive to observed variations in dry and wet aerosol refractive index and to changes in the height of the well-mixed surface layer. We expect these findings to be applicable to other moderately polluted and background continental air masses in which an accumulation mode between 0.1-0.5 µm diameter dominates aerosol extinction.

  7. Optical properties of aerosol contaminated cloud derived from MODIS instrument

    NASA Astrophysics Data System (ADS)

    Mei, Linlu; Rozanov, Vladimir; Lelli, Luca; Vountas, Marco; Burrows, John P.

    2016-04-01

    The presence of absorbing aerosols above/within cloud can reduce the amount of up-welling radiation in visible (VIS) and short-wave infrared and darken the spectral reflectance when compared with a spectrum of a clean cloud observed by satellite instruments (Jethva et al., 2013). Cloud properties retrieval for aerosol contaminated cases is a great challenge. Even small additional injection of aerosol particles into clouds in the cleanest regions of Earth's atmosphere will cause significant effect on those clouds and on climate forcing (Koren et al., 2014; Rosenfeld et al., 2014) because the micro-physical cloud process are non-linear with respect to the aerosol loading. The current cloud products like Moderate Resolution Imaging Spectroradiometer (MODIS) ignoring the aerosol effect for the retrieval, which may cause significant error in the satellite-derived cloud properties. In this paper, a new cloud properties retrieval method, considering aerosol effect, based on the weighting-function (WF) method, is presented. The retrieval results shows that the WF retrieved cloud properties (e.g COT) agrees quite well with MODIS COT product for relative clear atmosphere (AOT ≤ 0.4) while there is a large difference for large aerosol loading. The MODIS COT product is underestimated for at least 2 - 3 times for AOT>0.4, and this underestimation increases with the increase of AOT.

  8. Aerosol Property Comparison Within and Above the ABL at the ARM Program SGP Site

    SciTech Connect

    Delle Monache, L

    2002-05-01

    This thesis determines what, if any, measurements of aerosol properties made at the Earth surface are representative of those within the entire air column. Data from the Atmospheric Radiation Measurement site at the Southern Great Plains, the only location in the world where ground-based and in situ airborne measurements are routinely made. Flight legs during the one-year period from March 2000 were categorized as either within or above the atmospheric boundary layer (ABL) by use of an objective mixing height determination technique. Correlations between aerosol properties measured at the surface and those within and above the ABL were computed. Aerosol extensive and intensive properties measured at the surface were found representative of values within the ABL, but not of within the free atmosphere.

  9. A new approach for retrieving the UV-vis optical properties of ambient aerosols

    NASA Astrophysics Data System (ADS)

    Bluvshtein, Nir; Flores, J. Michel; Segev, Lior; Rudich, Yinon

    2016-08-01

    Atmospheric aerosols play an important part in the Earth's energy budget by scattering and absorbing incoming solar and outgoing terrestrial radiation. To quantify the effective radiative forcing due to aerosol-radiation interactions, researchers must obtain a detailed understanding of the spectrally dependent intensive and extensive optical properties of different aerosol types. Our new approach retrieves the optical coefficients and the single-scattering albedo of the total aerosol population over 300 to 650 nm wavelength, using extinction measurements from a broadband cavity-enhanced spectrometer at 315 to 345 nm and 390 to 420 nm, extinction and absorption measurements at 404 nm from a photoacoustic cell coupled to a cavity ring-down spectrometer, and scattering measurements from a three-wavelength integrating nephelometer. By combining these measurements with aerosol size distribution data, we retrieved the time- and wavelength-dependent effective complex refractive index of the aerosols. Retrieval simulations and laboratory measurements of brown carbon proxies showed low absolute errors and good agreement with expected and reported values. Finally, we implemented this new broadband method to achieve continuous spectral- and time-dependent monitoring of ambient aerosol population, including, for the first time, extinction measurements using cavity-enhanced spectrometry in the 315 to 345 nm UV range, in which significant light absorption may occur.

  10. Water nucleation properties of chaparral fire aerosol particles

    SciTech Connect

    Hudson, J.G.; Rogers, C.F.; Hallett, J.

    1989-05-01

    In December, 1986, planned and prescribed forest management burns took place at Lodi Canyon, on the north side of the Los Angeles Basin, California. These fires involved a mixture of species of small trees and shrubs, including scrub oak, chamise, and mountain mahogany, known collectively as ''chaparral'' in the Western US. Over a period of about two weeks, about 200 hectares of chaparral were consumed. This prescribed burn presented an opportunity for three days of airborne measurements of aerosol properties including total particle or condensation nuclei (CN) concentrations and cloud condensation nuclei (CCN) concentrations. This study is in coordination with other efforts conducted simultaneously; here the emphasis will be on the airborne CN and CCN measurements and on related studies conducted on a laboratory scale. In this study, we distinguish between CCN and the total aerosol particle population as gauged by the CN count. CCN and CN concentrations and CCN/CN ratios will be presented for the airborne measurements and for laboratory measurements employing a similar fuel. Ancillary ion chromatography (IC) and scanning electron microscopy (SEM) information will also be presented for the laboratory-scale chaparral burn. 11 refs., 4 figs., 4 tabs.

  11. Evolution of the Physicochemical and Activation Properties of Aerosols within Smoke Plumes during the Biomass Burning Observation Project (BBOP)

    NASA Astrophysics Data System (ADS)

    Tomlinson, J. M.; Mei, F.; Wang, J.; Comstock, J. M.; Hubbe, J. M.; Pekour, M. S.; Shilling, J. E.; Fortner, E.; Chand, D.; Sedlacek, A. J., III; Kleinman, L. I.; Senum, G.; Schmid, B.

    2014-12-01

    Biomass burning from wildfires and controlled agricultural burns are known to be a major source of fine particles and organic aerosols at northern temperate latitudes during the summer months. However, the evolution of the physicochemical properties of the aerosol during transport and the potential impact of this evolution on cloud condensation nuclei (CCN) activity has rarely been studied for these events. During the DOE-sponsored Biomass Burning Observation Project (BBOP) conducted in the summer and fall of 2013, over 30 research flights sampled biomass burning plumes from wildfires in the Northwestern United States and agricultural burns in the Mid-South region of the United States. A large suite of instruments aboard the DOE G-1 (Gulfstream-1) measured the chemical, physical, and optical properties of biomass burning aerosol with an emphasis on black carbon. A Fast Integrated Mobility Spectrometer (FIMS), Ultra High Sensitivity Aerosol Spectrometer - Airborne (UHSAS-A), and Passive Cavity Aerosol Spectrometer (PCASP) were used to measure the aerosol size distribution from 15 - 3,000 nm at 1-Hz. A dual column CCN counter measured the CCN number concentration at supersaturations of 0.25% and 0.50% at a time resolution of 1-Hz and the aerosol chemical composition was measured using a soot particle aerosol mass spectrometer (SP-AMS, Aerodyne, Inc). The SP-AMS was operated in two modes: (i) as a traditional high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS, Aerodyne Inc.), which measured chemical composition of non-refractory aerosols and (ii) as the SP-AMS which measured chemical composition of the refractory black carbon-containing (rBC) particle coating and rBC aerosol mass. Utilizing the aforementioned measurements, a CCN closure study is used to investigate the emitted aerosol hygroscopicity, the evolution of the physicochemical properties of the aerosol, and the potential impacts on cloud microphysics from the different fuel sources.

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

    NASA Astrophysics Data System (ADS)

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

    2010-01-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2010-05-01

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

  14. Satellite remote sensing of aerosol and cloud properties over Eurasia

    NASA Astrophysics Data System (ADS)

    Sogacheva, Larisa; Kolmonen, Pekka; Saponaro, Giulia; Virtanen, Timo; Rodriguez, Edith; Sundström, Anu-Maija; Atlaskina, Ksenia; de Leeuw, Gerrit

    2015-04-01

    Satellite remote sensing provides the spatial distribution of aerosol and cloud properties over a wide area. In our studies large data sets are used for statistical studies on aerosol and cloud interaction in an area over Fennoscandia, the Baltic Sea and adjacent regions over the European mainland. This area spans several regimes with different influences on aerosol cloud interaction such as a the transition from relative clean air over Fennoscandia to more anthropogenically polluted air further south, and the influence maritime air over the Baltic and oceanic air advected from the North Atlantic. Anthropogenic pollution occurs in several parts of the study area, and in particular near densely populated areas and megacities, but also in industrialized areas and areas with dense traffic. The aerosol in such areas is quite different from that produced over the boreal forest and has different effects on air quality and climate. Studies have been made on the effects of aerosols on air quality and on the radiation balance in China. The aim of the study is to study the effect of these different regimes on aerosol-cloud interaction using a large aerosol and cloud data set retrieved with the (Advanced) Along Track Scanning Radiometer (A)ATSR Dual View algorithm (ADV) further developed at Finnish Meteorological Institute and aerosol and cloud data provided by MODIS. Retrieval algorithms for aerosol and clouds have been developed for the (A)ATSR, consisting of a series of instruments of which we use the second and third one: ATSR-2 which flew on the ERS-2 satellite (1995-2003) and AATSR which flew on the ENVISAT satellite (2002-2012) (both from the European Space Agency, ESA). The ADV algorithm provides aerosol data on a global scale with a default resolution of 10x10km2 (L2) and an aggregate product on 1x1 degree (L3). Optional, a 1x1 km2 retrieval products is available over smaller areas for specific studies. Since for the retrieval of AOD no prior knowledge is needed on

  15. Long term aerosol and trace gas measurements in Central Amazonia

    NASA Astrophysics Data System (ADS)

    Artaxo, Paulo; Barbosa, Henrique M. J.; Ferreira de Brito, Joel; Carbone, Samara; Rizzo, Luciana V.; Andreae, Meinrat O.; Martin, Scot T.

    2016-04-01

    The central region of the Amazonian forest is a pristine region in terms of aerosol and trace gases concentrations. In the wet season, Amazonia is actually one of the cleanest continental region we can observe on Earth. A long term observational program started 20 years ago, and show important features of this pristine region. Several sites were used, between then ATTO (Amazon Tall Tower Observatory) and ZF2 ecological research site, both 70-150 Km North of Manaus, receiving air masses that traveled over 1500 km of pristine tropical forests. The sites are GAW regional monitoring stations. Aerosol chemical composition (OC/EC and trace elements) is being analysed using filters for fine (PM2.5) and coarse mode aerosol as well as Aerodyne ACSM (Aerosol Chemical Speciation Monitors). VOCs are measured using PTR-MS, while CO, O3 and CO2 are routinely measured. Aerosol absorption is being studied with AE33 aethalometers and MAAP (Multi Angle Absorption Photometers). Aerosol light scattering are being measured at several wavelengths using TSI and Ecotech nephelometers. Aerosol size distribution is determined using scanning mobility particle sizer at each site. Lidars measure the aerosol column up to 12 Km providing the vertical profile of aerosol extinction. The aerosol column is measures using AERONET sun photometers. In the wet season, organic aerosol comprises 75-85% of fine aerosol, and sulfate and nitrate concentrations are very low (1-3 percent). Aerosols are dominated by biogenic primary particles as well as SOA from biogenic precursors. Black carbon in the wet season accounts for 5-9% of fine mode aerosol. Ozone in the wet season peaks at 10-12 ppb at the middle of the day, while carbon monoxide averages at 50-80 ppb. Aerosol optical thickness (AOT) is a low 0.05 to 0.1 at 550 nm in the wet season. Sahara dust transport events sporadically enhance the concentration of soil dust aerosols and black carbon. In the dry season (August-December), long range transported

  16. CART and GSFC raman lidar measurements of atmospheric aerosol backscattering and extinction profiles for EOS validation and ARM radiation studies

    NASA Technical Reports Server (NTRS)

    Ferrare, R. A.; Turner, D. D.; Melfi, S. H.; Whiteman, D. N.; Schwenner, G.; Evans, K. D.; Goldsmith, J. E. M.; Tooman, T.

    1998-01-01

    The aerosol retrieval algorithms used by the Moderate-Resolution Imaging Spectroradiometer (MODIS) and Multi-Angle Imaging SpectroRadiometer (MISR) sensors on the Earth Observing Satellite (EOS) AM-1 platform operate by comparing measured radiances with tabulated radiances that have been computed for specific aerosol models. These aerosol models are based almost entirely on surface and/or column averaged measurements and so may not accurately represent the ambient aerosol properties. Therefore, to validate these EOS algorithms and to determine the effects of aerosols on the clear-sky radiative flux, we have begun to evaluate the vertical variability of ambient aerosol properties using the aerosol backscattering and extinction profiles measured by the Cloud and Radiation Testbed (CART) and NASA Goddard Space Flight Center (GSFC) Raman Lidars. Using the procedures developed for the GSFC Scanning Raman Lidar (SRL), we have developed and have begun to implement algorithms for the CART Raman Lidar to routinely provide profiles of aerosol extinction and backscattering during both nighttime and ,daytime operations. Aerosol backscattering and extinction profiles are computed for both lidar systems using data acquired during the 1996 and 1997 Water Vapor Intensive Operating Periods (IOPs). By integrating these aerosol extinction profiles, we derive measurements of aerosol optical thickness and compare these with coincident sun photometer measurements. We also use these measurements to measure the aerosol extinction/backscatter ratio S(sub a) (i.e. 'lidar ratio'). Furthermore, we use the simultaneous water vapor measurements acquired by these Raman lidars to investigate the effects of water vapor on aerosol optical properties.

  17. Aerosol and Cloud Microphysical Properties in the Asir region of Saudi Arabia

    NASA Astrophysics Data System (ADS)

    Axisa, Duncan; Kucera, Paul; Burger, Roelof; Li, Runjun; Collins, Don; Freney, Evelyn; Posada, Rafael; Buseck, Peter

    2010-05-01

    In recent advertent and inadvertent weather modification studies, a considerable effort has been made to understand the impact of varying aerosol properties and concentration on cloud properties. Significant uncertainties exist with aerosol-cloud interactions for which complex microphysical processes link the aerosol and cloud properties. Under almost all environmental conditions, increased aerosol concentrations within polluted air masses will enhance cloud droplet concentration relative to that in unperturbed regions. The interaction between dust particles and clouds are significant, yet the conditions in which dust particles become cloud condensation nuclei (CCN) are uncertain. In order to quantify this aerosol effect on clouds and precipitation, a field campaign was launched in the Asir region of Saudi Arabia as part of a Precipitation Enhancement Feasibility Study. Ground measurements of aerosol size distributions, hygroscopic growth factor, CCN concentrations as well as aircraft measurements of cloud hydrometeor size distributions were done in the Asir region of Saudi Arabia in August 2009. Research aircraft operations focused primarily on conducting measurements in clouds that are targeted for cloud top-seeding, on their microphysical characterization, especially the preconditions necessary for precipitation; understanding the evolution of droplet coalescence, supercooled liquid water, cloud ice and precipitation hydrometeors is necessary if advances are to be made in the study of cloud modification by cloud seeding. Non-precipitating mixed-phase clouds less than 3km in diameter that developed on top of the stable inversion were characterized by flying at the convective cloud top just above the inversion. Aerosol measurements were also done during the climb to cloud base height. The presentation will include a summary of the analysis and results with a focus on the unique features of the Asir region in producing convective clouds, characterization of the

  18. Aerosol properties over south india during different seasons

    NASA Astrophysics Data System (ADS)

    Sivaprasad, P.; Babu, C. A.; Jayakrishnan, P. R.

    Aerosols play an important role in the radiation balance and cloud properties, thereby affect the entire climatology of the earth-atmosphere system. Besides natural sources like dust, seasalt and natural sulphates, anthropogenic activities also inject aerosols like soot and industrial sulphates. Of these sea-salt and sulphates scatter the solar radiation. Soot is an absorbing aerosol while soil dust and organic matters are partly absorbing aerosols. Wind and rainfall are major factors affecting the transportation and deposition of the aerosols. India is a country blessed with plenty of monsoon rains. Winter (December to February), summer (March to May), monsoon (June to September) and post monsoon (October to November) are the four seasons over the region. Aerosol properties vary according to the season. Natural aerosols blown from the deserts have a major role in the aerosol optical depth over India. Of this, dust from Arabian desert that is carried by the winds are most important. The aerosol optical depth of south India is entirely different from that of north India. Maximum aerosol concentration is found over Gangetic plane in most of the seasons, whereas entire south India shows less aerosol optical depth. In the present study the aerosol properties of south India is analysed in general. Particular analysis is carried out for the four regions in the east and west coasts around Chennai, Kolkotha, Mumbai and Cochin. Chennai and Kolkotha are situated in the east coast whereas Cochin and Mumbai are in the west coast. These are industrial cities in India. Chennai region does not get monsoon rainfall since it is situated in the leeward side of Western ghats. But in the post monsoon season Chennai gets good amount of rainfall. Other three regions get good amount of rainfall during monsoon season. The study uses Terra MODIS, TOMS, NCEP/NCAR and TRMM data. Aerosol properties are analysed using Terra MODIS and Nimbus TOMS data. The variations of the aerosol optical

  19. Direct measurements of mass-specific optical cross sections of single-component aerosol mixtures.

    PubMed

    Radney, James G; Ma, Xiaofei; Gillis, Keith A; Zachariah, Michael R; Hodges, Joseph T; Zangmeister, Christopher D

    2013-09-01

    The optical properties of atmospheric aerosols vary widely, being dependent upon particle composition, morphology, and mixing state. This diversity and complexity of aerosols motivates measurement techniques that can discriminate and quantify a variety of single- and multicomponent aerosols that are both internally and externally mixed. Here, we present a new combination of techniques to directly measure the mass-specific extinction and absorption cross sections of laboratory-generated aerosols that are relevant to atmospheric studies. Our approach employs a tandem differential mobility analyzer, an aerosol particle mass analyzer, cavity ring-down and photoacoustic spectrometers, and a condensation particle counter. This suite of instruments enables measurement of aerosol particle size, mass, extinction and absorption coefficients, and aerosol number density, respectively. Taken together, these observables yield the mass-specific extinction and absorption cross sections without the need to model particle morphology or account for sample collection artifacts. Here we demonstrate the technique in a set of case studies which involve complete separation of aerosol by charge, separation of an external mixture by mass, and discrimination between particle types by effective density and single-scattering albedo. PMID:23875772

  20. Aerosol climatology from ground-based measurements for the southern North Sea

    NASA Astrophysics Data System (ADS)

    Behnert, Irina; Matthias, Volker; Doerffer, Roland

    2007-05-01

    An aerosol climatology over the southern North Sea region has been set up using aerosol optical properties derived from regular sunphotometer (AERONET) and lidar (EARLINET) measurements between April and September for the years 2000-2003. Data from four AERONET sites in the North Sea coastal region (Helgoland Island, Oostende, Hamburg and Lille) and, for comparison purposes, also from two "maritime sites" (Rame Head and Azores Island) are selected. The variability of the aerosol optical depth τa(500) and the spatial distribution of aerosol optical depth τa(500), Ångström wavelength exponent α440-870 , as well as of retrieved microphysical aerosol parameters (single scattering albedo, index of refraction, particle size distribution) are studied. The 4 years of observations show great similarities between the North Sea coastal sites and Helgoland Island. Although 70 km separated from the coast, the aerosol optical properties found at the island are much closer to those at Hamburg, Oostende and Lille than at the maritime sites Rame Head and Azores. Compared to the standard aerosol models differences in the Ångström wavelength exponent α440-870 , the single scattering albedo and the refractive index are detected. Based on these observations a new aerosol model for the atmospheric correction of coastal water reflectance spectra of the imaging spectrometer MERIS/ENVISAT was set up, which meets in particular the higher Ångström wavelength exponent of the coastal sites compared to standard maritime conditions.

  1. Meteorological and Aerosol effects on Marine Cloud Microphysical Properties

    NASA Astrophysics Data System (ADS)

    Sanchez, K. J.; Russell, L. M.; Modini, R. L.; Frossard, A. A.; Ahlm, L.; Roberts, G.; Hawkins, L. N.; Schroder, J. C.; Wang, Z.; Lee, A.; Abbatt, J.; Lin, J.; Nenes, A.; Wonaschuetz, A.; Sorooshian, A.; Noone, K.; Jonsson, H.; Albrecht, B. A.; Desiree, T. S.; Macdonald, A. M.; Seinfeld, J.; Zhao, R.

    2015-12-01

    Both meteorology and microphysics affect cloud formation and consequently their droplet distributions and shortwave reflectance. The Eastern Pacific Emitted Aerosol Cloud Experiment (EPEACE) and the Stratocumulus Observations of Los-Angeles Emissions Derived Aerosol-Droplets (SOLEDAD) studies provide detailed measurements in 6 case studies of both cloud thermodynamic properties and initial particle number distribution and composition, as well as the resulting cloud drop distribution and composition. This study uses simulations of a detailed chemical and microphysical aerosol-cloud parcel (ACP) model with explicit kinetic drop activation to reproduce the observed cloud droplet distribution and composition. Four of the cases examined had a sub-adiabatic lapse rate, which was shown to have fewer droplets due to decreased maximum supersaturation, lower LWC and higher cloud base height, consistent with previous findings. These detailed case studies provided measured thermodynamics and microphysics that constrained the simulated droplet size distribution sufficiently to match the droplet number within 6% and the size within 19% for 4 of the 6 cases, demonstrating "closure" or consistency of the measured composition with the measured CCN spectra and the inferred and modeled supersaturation. The contribution of organic components to droplet formation shows small effects on the droplet number and size in the 4 marine cases that had background aerosol conditions with varying amounts of coastal, ship or other non-biogenic sources. In contrast, the organic fraction and hygroscopicity increased the droplet number and size in the cases with generated smoke and cargo ship plumes that were freshly emitted and not yet internally mixed with the background particles. The simulation results show organic hygroscopicity causes small effects on cloud reflectivity (<0.7%) with the exception of the cargo ship plume and smoke plume which increased absolute cloud reflectivity fraction by 0

  2. 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.

  3. Estimation of aerosol optical properties from all-sky imagers

    NASA Astrophysics Data System (ADS)

    Kazantzidis, Andreas; Tzoumanikas, Panagiotis; Salamalikis, Vasilios; Wilbert, Stefan; Prahl, Christoph

    2015-04-01

    Aerosols are one of the most important constituents in the atmosphere that affect the incoming solar radiation, either directly through absorbing and scattering processes or indirectly by changing the optical properties and lifetime of clouds. Under clear skies, aerosols become the dominant factor that affect the intensity of solar irradiance reaching the ground. It has been shown that the variability in direct normal irradiance (DNI) due to aerosols is more important than the one induced in global horizontal irradiance (GHI), while the uncertainty in its calculation is dominated by uncertainties in the aerosol optical properties. In recent years, all-sky imagers are used for the detection of cloud coverage, type and velocity in a bouquet of applications including solar irradiance resource and forecasting. However, information about the optical properties of aerosols could be derived with the same instrumentation. In this study, the aerosol optical properties are estimated with the synergetic use of all-sky images, complementary data from the Aerosol Robotic Network (AERONET) and calculations from a radiative transfer model. The area of interest is Plataforma Solar de Almería (PSA), Tabernas, Spain and data from a 5 month period are analyzed. The proposed methodology includes look-up-tables (LUTs) of diffuse sky radiance of Red (R), Green (G) and Blue (B) channels at several zenith and azimuth angles and for different atmospheric conditions (Angström α and β, single scattering albedo, precipitable water, solar zenith angle). Based on the LUTS, results from the CIMEL photometer at PSA were used to estimate the RGB radiances for the actual conditions at this site. The methodology is accompanied by a detailed evaluation of its robustness, the development and evaluation of the inversion algorithm (derive aerosol optical properties from RGB image values) and a sensitivity analysis about how the pre-mentioned atmospheric parameters affect the results.

  4. Determination of aerosol size distributions from spectral attenuation measurements.

    PubMed

    Grassl, H

    1971-11-01

    An iteration method for the determination of size distributions of aerosols from spectral attenuation data, similar to the one previously published for clouds, is presented. The basis for this iteration is to consider the extinction efficiency factor of particles as a set of weighting functions covering the entire radius region of a distribution. The weighting functions were calculated exactly from the Mie theory. Aerosol distributions are shown derived from tests with analytical size distributions and also generated from measured aerosol extinction data in seven spectral channels from 0.4-microto 10-micro wavelength in continental aerosols. The influence of relative humidity on the complex index of refraction is also discussed.

  5. Cloud-Aerosol Interactions: Retrieving Aerosol Ångström Exponents from Calipso Measurements of Opaque Water Clouds

    NASA Astrophysics Data System (ADS)

    Vaughan, Mark; Liu, Zhaoyan; Hu, Yong-Xiang; Powell, Kathleen; Omar, Ali; Rodier, Sharon; Hunt, William; Kar, Jayanta; Tackett, Jason; Getzewich, Brian; Lee, Kam-Pui

    2016-06-01

    Backscatter and extinction from water clouds are well-understood, both theoretically and experimentally, and thus changes to the expected measurement of layer-integrated attenuated backscatter can be used to infer the optical properties of overlying layers. In this paper we offer a first look at a new retrieval technique that uses CALIPSO measurements of opaque water clouds to derive optical depths and Ångström exponents for overlying aerosol layers.

  6. Retrieval of Aerosol Parameters from Continuous H24 Lidar-Ceilometer Measurements

    NASA Astrophysics Data System (ADS)

    Dionisi, D.; Barnaba, F.; Costabile, F.; Di Liberto, L.; Gobbi, G. P.; Wille, H.

    2016-06-01

    Ceilometer technology is increasingly applied to the monitoring and the characterization of tropospheric aerosols. In this work, a method to estimate some key aerosol parameters (extinction coefficient, surface area concentration and volume concentration) from ceilometer measurements is presented. A numerical model has been set up to derive a mean functional relationships between backscatter and the above mentioned parameters based on a large set of simulated aerosol optical properties. A good agreement was found between the modeled backscatter and extinction coefficients and the ones measured by the EARLINET Raman lidars. The developed methodology has then been applied to the measurements acquired by a prototype Polarization Lidar-Ceilometer (PLC). This PLC instrument was developed within the EC- LIFE+ project "DIAPASON" as an upgrade of the commercial, single-channel Jenoptik CHM15k system. The PLC run continuously (h24) close to Rome (Italy) for a whole year (2013-2014). Retrievals of the aerosol backscatter coefficient at 1064 nm and of the relevant aerosol properties were performed using the proposed methodology. This information, coupled to some key aerosol type identification made possible by the depolarization channel, allowed a year-round characterization of the aerosol field at this site. Examples are given to show how this technology coupled to appropriate data inversion methods is potentially useful in the operational monitoring of parameters of air quality and meteorological interest.

  7. Aerosol measurements at a high-elevation site: composition, size, and cloud condensation nuclei activity

    SciTech Connect

    Friedman, Beth; Zelenyuk, Alla; Beranek, Josef; Kulkarni, Gourihar R.; Pekour, Mikhail S.; Hallar, Anna G.; McCubbin, Ian; Thornton, Joel A.; Cziczo, D. J.

    2013-12-09

    We present measurements of CCN concentrations and associated aerosol composition and size properties at a high-elevation research site in March 2011. CCN closure and aerosol hygroscopicity were assessed using simplified assumptions of bulk aerosol properties as well as a new method utilizing single particle composition and size to assess the importance of particle mixing state in CCN activation. Free troposphere analysis found no significant difference between the CCN activity of free tropospheric aerosol and boundary layer aerosol at this location. Closure results indicate that using only size and number information leads to adequate prediction, in the majority of cases within 50%, of CCN concentrations, while incorporating the hygroscopicity parameters of the individual aerosol components measured by single particle mass spectrometry adds to the agreement, in most cases within 20%, between predicted and measured CCN concentrations. For high-elevation continental sites, with largely aged aerosol and low amounts of local area emissions, a lack of chemical knowledge and hygroscopicity may not hinder models in predicting CCN concentrations. At sites influenced by fresh emissions or more heterogeneous particle types, single particle composition information may be more useful in predicting CCN concentrations and understanding the importance of particle mixing state on CCN activation.

  8. 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.

  9. Light scattering and absorption properties of aerosol particles in the urban environment of Granada, Spain

    NASA Astrophysics Data System (ADS)

    Lyamani, H.; Olmo, F. J.; Alados-Arboledas, L.

    Surface measurements of optical and physical aerosol properties were made at an urban site, Granada (Spain) (37.18°N, 3.58°W, 680 m a.s.l), during winter 2005-2006. Measurements included the aerosol scattering, σsca, and backscattering coefficients, σbsca, at three wavelengths (450, 550 and 700 nm) measured at low relative humidity (RH<50%) by an integrating nephelometer, the absorption coefficient at 670 nm, σabs, measured with a multi-angle absorption photometer, and aerosol size distribution in the 0.5-20 μm aerodynamic diameter range registered by an aerodynamic aerosol sizer (APS-3321, TSI). The hourly average of σsca (550 nm) ranged from 2 to 424 M m -1 with an average value of 84±62 M m -1 (±S.D.). The Angstrom exponent presented an average value of 1.8±0.3, suggesting a large fraction of fine particles at the site, an observation confirmed by aerosol size distribution measurements. The hourly average of σabs (670 nm) ranged from 1.7 to 120.5 M m -1 with an average value of 28±20 M m -1. The results indicate that the aerosol absorption coefficient in Granada was relatively large. The largest σsca value was associated with air masses that passed over heavily polluted European areas and local stagnation conditions. High absorbing aerosol level was obtained during dust transport from North Africa probably due to the presence of hematite. Based on the measured scattering and absorption coefficients, a very low average value of the single scattering albedo of 0.66±0.11 at 670 nm was calculated, suggesting that urban aerosols in this region contain a large fraction of absorbing material. A clear diurnal pattern was observed in scattering and absorption coefficients and particle concentrations with two local maxima occurring in early morning and late evening. This behavior can be explained in terms of local conditions that control the particle sources associated with traffic and upward mixing of the aerosol during the daytime development of a

  10. Aerosol light scattering measurements as a function of relative humidity.

    PubMed

    Day, D E; Malm, W C; Kreidenweis, S M

    2000-05-01

    The hygroscopic nature of atmospheric fine aerosol was investigated at a rural site in the Great Smoky Mountains National Park during July and August 1995. Passing the sample aerosol through an inlet, which housed an array of Perma Pure diffusion dryers, controlled the sample aerosol's relative humidity (RH). After conditioning the aerosol sample in the inlet, the light scattering coefficient and the aerosol size distribution were simultaneously measured. During this study, the conditioned aerosol's humidity ranged between 5% < RH < 95%. Aerosol response curves were produced using the ratio bspw/bspd; where bspw is the scattering coefficient measured at some RH greater than 20% and bspd is the scattering coefficient of the "dry" aerosol. For this work, any sample RH values below 15% were considered dry. Results of this investigation showed that the light scattering ratio increased continuously and smoothly over the entire range of relative humidity. The magnitude of the ratio at a particular RH value, however, varied considerably in time, particularly for RH values greater than approximately 60%. Curves of the scattering coefficient ratios as a function of RH were generated for each day and compared to the average 12-hour chemical composition of the aerosol. This comparison showed that for any particular RH value the ratio was highest during time periods of high sulfate concentrations and lowest during time periods of high soil or high organic carbon concentrations.

  11. Aerosol properties from 4STAR observations: A sensitivity study

    NASA Astrophysics Data System (ADS)

    Kassianov, E.; Flynn, C.; Redemann, J.; Livingston, J. M.; Schmid, B.; Russell, P. B.; Sinyuk, A.

    2011-12-01

    Multi-spectral direct-beam observations of atmospheric aerosol and gas constituents have been taken successfully at a number of sites around the world by the airborne 14-Channel NASA Ames Airborne Tracking Sunphotometer (AATS-14). The recently developed airborne Spectrometer for Sky-Scanning, Sun-Tracking Atmospheric Research (4STAR) is the next generation of AATS-14 with ultraviolet, visible and near-infrared spectral coverage, increased number of channels (more than 1500 pixels) and the sky-scanning ability of the ground-based AERONET sun/sky photometers. While it is generally agreed that more measurements in terms of independent wavelengths and scattering angles would offer enhanced aerosol retrievals, the potential afforded by improved observational capabilities of the 4STAR has not yet been fully characterized. This paper will attempt to place the importance of improved spectrally- and angularly-resolved 4STAR observations within the context of the well-known AERONET intensive-property retrieval. In particular, we have developed model data sets comparable to the 4STAR measurements of direct sun and sky radiances and evaluated the impact on the retrieval from subsampling in wavelength and scattering angle.

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

    NASA Technical Reports Server (NTRS)

    Levy, Robert C.; Pinker, Rachel T.

    2006-01-01

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

  13. Morphology and Optical Properties of Mixed Aerosol Particles

    NASA Astrophysics Data System (ADS)

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

    2016-04-01

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

  14. Spatial characteristics of aerosol physical properties over the northeastern parts of peninsular India

    NASA Astrophysics Data System (ADS)

    Niranjan, K.; Melleswara Rao, B.; Brahmanandam, P. S.; Madhavan, B. L.; Sreekanth, V.; Krishna Moorthy, K.

    2005-11-01

    Measurements on aerosol spectral optical depths and near surface mass-size distributions made at several locations in the states of Andhra Pradesh, Orissa and Chattisgarh, constituting the northeastern part of the peninsular India during the ISRO-GBP land campaign-I show significant regional variations in aerosol physical properties. Higher spectral optical depths were observed in the coastal regions and over southern latitudes compared to interior continental regions and northern latitudes. The optical depths, size index "α" and the near surface aerosol mass concentrations indicate a relative abundance of nucleation mode aerosols in the northern latitudes, in contrast to the dominance of the accumulation mode aerosols at the eastern coastal and southern latitudes. The airmass pathways derived from the back trajectory analysis indicate that the higher aerosol population in the accumulation mode, and consequently the higher optical depths in the southern locations, could be due to the transport of aerosol from the polluted north Indian regions via the oceanic region over the Bay of Bengal, where significant particle growth is expected, increasing the population of accumulation mode aerosols over these regions.

  15. Biomass Burning Aerosol Absorption Measurements with MODIS Using the Critical Reflectance Method

    NASA Technical Reports Server (NTRS)

    Zhu, Li; Martins, Vanderlei J.; Remer, Lorraine A.

    2010-01-01

    This research uses the critical reflectance technique, a space-based remote sensing method, to measure the spatial distribution of aerosol absorption properties over land. Choosing two regions dominated by biomass burning aerosols, a series of sensitivity studies were undertaken to analyze the potential limitations of this method for the type of aerosol to be encountered in the selected study areas, and to show that the retrieved results are relatively insensitive to uncertainties in the assumptions used in the retrieval of smoke aerosol. The critical reflectance technique is then applied to Moderate Resolution Imaging Spectrometer (MODIS) data to retrieve the spectral aerosol single scattering albedo (SSA) in South African and South American 35 biomass burning events. The retrieved results were validated with collocated Aerosol Robotic Network (AERONET) retrievals. One standard deviation of mean MODIS retrievals match AERONET products to within 0.03, the magnitude of the AERONET uncertainty. The overlap of the two retrievals increases to 88%, allowing for measurement variance in the MODIS retrievals as well. The ensemble average of MODIS-derived SSA for the Amazon forest station is 0.92 at 670 nm, and 0.84-0.89 for the southern African savanna stations. The critical reflectance technique allows evaluation of the spatial variability of SSA, and shows that SSA in South America exhibits higher spatial variation than in South Africa. The accuracy of the retrieved aerosol SSA from MODIS data indicates that this product can help to better understand 44 how aerosols affect the regional and global climate.

  16. Retrieval of aerosol optical and micro-physical properties with 2D-MAX-DOAS

    NASA Astrophysics Data System (ADS)

    Ortega, Ivan; Coburn, Sean; Hostetler, Chris; Ferrare, Rich; Hair, Johnathan; Kassianov, Evgueni; Barnard, James; Berg, Larry; Schmid, Beat; Tomlinson, Jason; Hodges, Gary; Lantz, Kathy; Wagner, Thomas; Volkamer, Rainer

    2015-04-01

    Recent retrievals of 2 dimensional (2D) Multi-AXis Differential Optical Absorption Spectroscopy (2D-MAX-DOAS) have highlighted its importance in order to infer diurnal horizontal in-homogeneities around the measurement site. In this work, we expand the capabilities of 2D measurements in order to estimate simultaneously aerosol optical and micro-physical properties. Specifically, we present a retrieval method to obtain: (1) aerosol optical thickness (AOT) in the boundary layer (BL) and free troposphere (FT) and (2) the effective complex refractive index and the effective radius of the aerosol column size distribution. The retrieval method to obtain AOT is based on an iterative comparison of measured normalized radiances, oxygen collision pair (O4), and absolute Raman Scattering Probability (RSP) with the forward model calculations derived with the radiative transfer model McArtim based on defined aerosol extinction profiles. Once the aerosol load is determined we use multiple scattering phase functions and single scattering albedo (SSA) obtained with Mie calculations which then constrain the RTM to forward model solar almucantar normalized radiances. The simulated almucantar normalized radiances are then compared to the measured normalized radiances. The best-fit, determined by minimizing the root mean square, retrieves the complex refractive index, and effective radius. We apply the retrieval approach described above to measurements carried out during the 2012 intensive operation period of the Two Column Aerosol Project (TCAP) held on Cape Cod, MA, USA. Results are presented for two ideal case studies with both large and small aerosol loading and similar air mass outflow from the northeast coast of the US over the West Atlantic Ocean. The aerosol optical properties are compared with several independent instruments, including the NASA Langley airborne High Spectral Resolution Lidar (HSRL-2) for highly resolved extinction profiles during the overpasses, and with the

  17. 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.

  18. New capabilities for space-based cloud and aerosols measurements: The Cloud-Aerosol Transport System (CATS)

    NASA Astrophysics Data System (ADS)

    Yorks, J. E.; McGill, M. J.; Hlavka, D. L.; Palm, S. P.; Hart, W. D.; Nowottnick, E. P.; Vaughan, M.; Rodier, S. D.; Colarco, P. R.; da Silva, A.; Buchard-Marchant, V.

    2013-12-01

    Current uncertainties in cloud and aerosol properties limit our ability to accurately model the Earth's climate system and predict climate change. These limitations are due primarily to difficulties in adequately measuring aerosols and clouds on a global scale. NASA's A-Train satellites provide an unprecedented opportunity to address these uncertainties. In particular, the Cloud-Aerosol Lidar Infrared Pathfinder Spaceborne Observations (CALIPSO) satellite provides vertical profiles of cloud and aerosol properties. The CALIOP lidar onboard CALIPSO has reached its seventh year of operation, well past its expected lifetime. The ATLID lidar on EarthCARE is not expected to launch until 2016 or later. If the CALIOP lidar fails before a new mission is operational, there will be a gap in global lidar measurements. The Cloud-Aerosol Transport System (CATS), built at NASA Goddard Space Flight Center as a payload for the International Space Station (ISS), is set to launch in the summer of 2014. CATS is an elastic backscatter lidar with three wavelengths (1064, 532, 355 nm) and HSRL capability at 532 nm. Depolarization measurements will be made at all three wavelengths. The ISS orbit is a 51 degree inclination orbit at an altitude of about 405 km. This orbit provides more comprehensive coverage of the tropics and mid-latitudes than sun-synchronous orbiting sensors, with nearly a three day repeat cycle. Thus, science applications of CATS include cloud and aerosol climate studies, air quality monitoring, and smoke/volcanic plume tracking. The primary science objectives of CATS include: continuing the CALIPSO aerosol and cloud vertical profile data record, providing near real time data to support operational applications such as air quality modeling, and advancing technology in support of future mission development using the HSRL channel. Furthermore, the vertical profiles of cloud and aerosol properties provided by CATS will complement current and future passive satellite

  19. Comparison Between Lidar and Nephelometer Measurements of Aerosol Hygroscopicity at the Southern Great Plains Atmospheric Radiation Measurement Site

    NASA Technical Reports Server (NTRS)

    Pahlow, M.; Feingold, G.; Jefferson, A.; Andrews, E.; Ogren, J. A.; Wang, J.; Lee, Y.-N.; Ferrare, R. A.

    2004-01-01

    Aerosol hygroscopicity has a significant effect on radiative properties of aerosols. Here a lidar method, applicable to cloud-capped, well-mixed atmospheric boundary layers, is employed to determine the hygroscopic growth factor f(RH) under unperturbed, ambient atmospheric conditions. The data used for the analysis were collected under a wide range of atmospheric aerosol levels during both routine measurement periods and during the intensive operations period (IOP) in May 2003 at the Southern Great Plains (SGP) Climate Research Facility in Oklahoma, USA, as part of the Atmospheric Radiation Measurement (ARM) program. There is a good correlation (approx. 0.7) between a lidar-derived growth factor (measured over the range 85% RH to 96% RH) with a nephelometer-derived growth factor measured over the RH range 40% to 85%. For these RH ranges, the slope of the lidar-derived growth factor is much steeper than that of the nephelometer-derived growth factor, reflecting the rapid increase in particle size with increasing RH. The results are corroborated by aerosol model calculations of lidar and nephelometer equivalent f(RH) based on in situ aerosol size and composition measurements during the IOP. It is suggested that the lidar method can provide useful measurements of the dependence of aerosol optical properties on relative humidity, and under conditions closer to saturation than can currently be achieved with humidified nephelometers.

  20. Aerosol Properties and Radiative Forcing over Mega-cities in China

    NASA Astrophysics Data System (ADS)

    Li, Z.

    2007-12-01

    As the fastest and largest developing country in the world, China is experiencing rapid environmental changes. High concentrations of aerosols with diverse properties are emitted in the region, providing a unique opportunity for understanding the impact of environmental changes on climate. Until very recently, few observational studies were conducted in this important source region. The East Asian Study of Tropospheric Aerosols: an International Regional Experiment (EAST-AIRE) attempts to characterize the physical, optical and chemical properties of the aerosols and their effects on climate over China. Some preliminary results will be presented using continuous high-quality measurements of aerosol, cloud and radiative quantities made at the EAST-AIRE baseline stations near two mega cities (Beijing and Shanhai) in northern and southern China. Both regions are often covered by a thick layer of haze (with a yearly mean aerosol optical depth 0.7-0.8) due primarily to anthropogenic emissions of moderately strong absorbing aerosols, leading exceptionally large aerosol radiative forcing.

  1. Airborne Measurements of Coarse Mode Aerosol Composition and Abundance

    NASA Astrophysics Data System (ADS)

    Froyd, K. D.; Murphy, D. M.; Brock, C. A.; Ziemba, L. D.; Anderson, B. E.; Wilson, J. C.

    2015-12-01

    Coarse aerosol particles impact the earth's radiative balance by direct scattering and absorption of light and by promoting cloud formation. Modeling studies suggest that coarse mode mineral dust and sea salt aerosol are the dominant contributors to aerosol optical depth throughout much of the globe. Lab and field studies indicate that larger aerosol particles tend to be more efficient ice nuclei, and recent airborne measurements confirm the dominant role of mineral dust on cirrus cloud formation. However, our ability to simulate coarse mode particle abundance in large scale models is limited by a lack of validating measurements above the earth's surface. We present airborne measurements of coarse mode aerosol abundance and composition over several mid-latitude, sub-tropical, and tropical regions from the boundary layer to the stratosphere. In the free troposphere the coarse mode constitutes 10-50% of the total particulate mass over a wide range of environments. Above North America mineral dust typically dominates the coarse mode, but biomass burning particles and sea salt also contribute. In remote environments coarse mode aerosol mainly consists of internally mixed sulfate-organic particles. Both continental and marine convection can enhance coarse aerosol mass through direct lofting of primary particles and by secondary accumulation of aerosol material through cloud processing.

  2. A study of regional aerosol radiative properties and effects on ultraviolet-B radiation

    NASA Astrophysics Data System (ADS)

    Wenny, B. N.; Schafer, J. S.; Deluisi, J. J.; Saxena, V. K.; Barnard, W. F.; Petropavlovskikh, I. V.; Vergamini, A. J.

    1998-07-01

    A field experiment was conducted in western North Carolina to investigate the relationship between aerosol optical properties and atmospheric transmission. Two research measurement sites in close horizontal proximity but at different altitudes were established to measure the transmission of UV radiation through a slab of atmosphere. An identical set of radiation sensing instruments, including a broadband UV-B radiometer, a direct Sun pyrheliometer, a shadowband radiometer, and a spectral photometer, was placed at both sites, a mountaintop site (Mount Gibbes 35.78°N, 82.29°W, 2004 m elevation) and a valley site (Black Mountain, North Carolina 35.66°N, 82.38°N, 951 m elevation). Aerosol size distribution sampling equipment was located at the valley site. Broadband solar pseudo-optical depth and aerosol optical depths at 415 nm, 500 nm, and 673 nm were measured for the lowest 1-km layer of the troposphere. The measurements exhibited variations based on an air mass source region as determined by back trajectory analysis. Broadband UV-B transmission through the layer also displayed variations relating to air mass source region. Spectral UV transmission revealed a dependence upon wavelength, with decreased transmission in the UV-B region (300-320 nm) versus UV-A region (320-363.5 nm). UV-B transmission was found to be negatively correlated with aerosol optical depth. Empirical relations were developed to allow prediction of solar noon UV-B transmission if aerosol optical depth at two visible wavelengths (415 and 500 nm) is known. A new method was developed for determining aerosol optical properties from the radiation and aerosol size distribution measurements. The aerosol albedo of single scatter was found to range from 0.75 to 0.93 and the asymmetry factor ranged from 0.63 to 0.76 at 312 nm, which is close to the peak response of human skin to UV radiation.

  3. Retrieval of optical and microphysical properties of aerosols from a hybrid multiwavelength lidar dataset

    NASA Astrophysics Data System (ADS)

    Sawamura, Patricia

    Over the past decade the development of inversion techniques for the retrievals of aerosol microphysical properties (e.g. effective radius, volume and surface-area concentrations) and aerosol optical properties (e.g. complex index of refraction and single scattering albedo) from multiwavelength lidar systems brought a new perspective in the study of the vertical distribution of aerosols. In this study retrievals of such parameters were obtained from a hybrid multiwavelength lidar dataset for the first time. In July of 2011, in the Baltimore-Washington DC region, synergistic profiling of optical and microphysical properties of aerosols with both airborne in-situ and ground-based remote sensing systems was performed during the first deployment of DISCOVER-AQ. The hybrid multiwavelength lidar dataset combines elastic ground-based measurements at 355 nm with airborne High Spectral Resolution Lidar (HSRL) measurements at 532 nm and elastic measurements at 1064 nm that were obtained less than 5 km apart of each other. This was the first study to our knowledge in which optical and microphysical retrievals from lidar were obtained during the day and directly compared to AERONET and in-situ measurements for eleven cases. Good agreement was observed between lidar and AERONET retrievals. Larger discrepancies were observed between lidar retrievals and in-situ measurements obtained by the aircraft and aerosol hygroscopic effects are believed to be the main factor of such discrepancies.

  4. Observed correlations between aerosol and cloud properties in an Indian Ocean trade cumulus regime

    NASA Astrophysics Data System (ADS)

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

    2015-10-01

    There are many contributing factors which determine the micro- and macrophysical properties of clouds, including atmospheric structure, dominant meteorological conditions, and aerosol concentration, all of which may be coupled to one another. In the quest to determine aerosol effects on clouds, these potential relationships must be understood, as changes in atmospheric conditions due to aerosol may change the expected magnitude of indirect effects by altering cloud properties in unexpected ways. Here we describe several observed correlations between aerosol conditions and cloud and atmospheric properties in the Indian Ocean winter monsoon season. In the CARDEX (Cloud, Aerosol, Radiative forcing, Dynamics EXperiment) field campaign conducted in February and March 2012 in the northern Indian Ocean, continuous measurements of atmospheric precipitable water vapor and the liquid water path (LWP) of trade cumulus clouds were made, concurrent with measurements of water vapor flux, cloud and aerosol vertical profiles, meteorological data, and surface and total-column aerosol. Here we present evidence of a positive correlation between aerosol and cloud LWP which becomes clear after the data are filtered to control for the natural meteorological variability in the region. We then use the aircraft and ground observatory measurements to explore the mechanisms behind the observed aerosol-LWP correlation. We determine that increased boundary-layer humidity lowering the cloud base is responsible for the observed increase in cloud liquid water. Large-scale analysis indicates that high pollution cases originate with a highly-polluted boundary layer air mass approaching the observatory from a northwesterly direction. This polluted mass exhibits higher temperatures and humidity than the clean case, the former of which may be attributable to heating due to aerosol absorption of solar radiation over the subcontinent. While high temperature conditions dispersed along with the high-aerosol

  5. Synergy of Satellite-Surface Observations for Studying the Properties of Absorbing Aerosols in Asia

    NASA Technical Reports Server (NTRS)

    Tsay, Si-Chee

    2010-01-01

    Through interaction with clouds and alteration of the Earth's radiation budget, atmospheric aerosols significantly influence our weather and climate. Monsoon rainfalls, for example, sustain the livelihood of more than half of the world's population. Thus, understanding the mechanism that drives the water cycle and freshwater distribution is high-lighted as one of the major near-term goals in NASA's Earth Science Enterprise Strategy. Every cloud droplet/ice-crystal that serves as an essential element in portraying water cycle and distributing freshwater contains atmospheric aerosols at its core. In addition, the spatial and temporal variability of atmospheric aerosol properties is complex due to their dynamic nature. In fact, the predictability of the tropical climate system is much reduced during the boreal spring, which is associated with the peak season of biomass burning activities and regional/long-range transport of dust aerosols. Therefore, to accurately assess the impact of absorbing aerosols on regional-to-global climate requires not only modeling efforts but also continuous observations from satellites, aircraft, networks of ground-based instruments and dedicated field experiments. Since 1997 NASA has been successfully launching a series of satellites the Earth Observing System - to intensively study, and gain a better understanding of, the Earth as an integrated system. Through participation in many satellite remote-sensing/retrieval and validation projects over the years, we have gradually developed and refined the SMART (Surface-sensing Measurements for Atmospheric Radiative Transfer) and COMMIT (Chemical, Optical & Microphysical Measurements of In-situ Troposphere) mobile observatories, a suite of surface remote sensing and in-situ instruments that proved to be vital in providing high temporal measurements, which complement the satellite observations. In this talk, we will present SMART-COMMIT which has played key roles, serving as network or supersite

  6. Improving satellite retrieved aerosol microphysical properties using GOCART data

    NASA Astrophysics Data System (ADS)

    Li, S.; Kahn, R.; Chin, M.; Garay, M. J.; Chen, L.; Liu, Y.

    2014-09-01

    The Multi-Angle Imaging Spectro-Radiometer (MISR) instrument on NASA's Terra satellite can provide more reliable Aerosol Optical Depth (AOD, τ) and more particle information, such as constraints on particle size (Angström exponent or ANG, α), particle shape, and single-scattering albedo (SSA, ω), than many other satellite instruments. However, MISR's ability to retrieve aerosol properties is weakened at low AOD levels. When aerosol-type information content is low, many candidate aerosol mixtures can match the observed radiances. We propose an algorithm to improve MISR aerosol retrievals by constraining MISR mixtures' ANG and absorbing AOD (AAOD) with Goddard Chemistry Aerosol Radiation and Transport (GOCART) model-simulated aerosol properties. To demonstrate this approach, we calculated MISR aerosol optical properties over the contiguous US from 2006 to 2009. Sensitivities associated with the thresholds of MISR-GOCART differences were analyzed according to the agreement between our results (AOD, ANG, and AAOD) and AErosol RObotic NETwork (AERONET) observations. Overall, our AOD has a good agreement with AERONET because the MISR AOD retrieval is not sensitive to different mixtures under many retrieval conditions. The correlation coefficient (r) between our ANG and AERONET improves to 0.45 from 0.29 for the MISR Version 22 standard product and 0.43 for GOCART when all data points are included. However, when only cases having AOD > 0.2, the MISR product itself has r ~ 0.40, and when only AOD > 0.2 and the best-fitting mixture are considered, r ~ 0.49. So as expected, the ANG improvement occurs primarily when the model constraint is applied in cases where the particle type information content of the MISR radiances is low. Regression analysis for AAOD shows that MISR Version 22 and GOCART misestimate AERONET by a ratio (mean retrieved AAOD to mean AERONET AAOD) of 0.5; our method improves this ratio to 0.74. Large discrepancies are found through an inter

  7. The thermal infrared radiance properties of dust aerosol over ocean

    NASA Astrophysics Data System (ADS)

    Hao, Zengzhou; Pan, Delu; Tu, Qianguang; Gong, Fang; Chen, Jianyu

    2015-10-01

    Asian dust storms, which can long-range transport to ocean, often occur on spring. The present of Asian dust aerosols over ocean makes some difficult for other studies, such as cloud detection, and also take some advantage for ocean, such as take nutrition into the ocean by dry or wet deposition. Therefore, it is important to study the dust aerosol and retrieve the properties of dust from satellite observations that is mainly from the thermal infrared radiance. In this paper, the thermal infrared radiance properties of dust aerosol over ocean are analyzed from MODIS and MTSAT2 observations and Streamer model simulations. By analyzing some line samples and a series of dust aerosol region, it shows that the dust aerosol brightness temperature at 12μm (BT12) is always greater than BT11 and BT8.5, and BT8.5 is general greater than BT11. The brightness temperature different between 11μm and 12μm (BTD11-12) increases with the dust intensity. And the BTD11-12 will become positive when the atmospheric relative humidity is greater than 70%. The BTD11-12 increases gradually with the surface temperature while the effect on BTD11-12 of dust layer temperature is not evident. Those are caused by the transmission of the dust aerosol is different at the two thermal infrared channels. During daytime, dust infrared brightness temperature at mid-infrared bands should reduce the visual radiance, which takes about 25K or less. In general, BT3.7 is greater than BT11 for dust aerosol. Those results are helpful to monitor or retrieve dust aerosol physical properties over ocean from satellite.

  8. Lidar backscattering measurements of background stratospheric aerosols

    NASA Technical Reports Server (NTRS)

    Remsberg, E. E.; Northam, G. B.; Butler, C. F.

    1979-01-01

    A comparative lidar-dustsonde experiment was conducted in San Angelo, Texas, in May 1974 in order to estimate the uncertainties in stratospheric-aerosol backscatter for the NASA Langley 48-inch lidar system. The lidar calibration and data-analysis procedures are discussed. Results from the Texas experiment indicate random and systematic uncertainties of 35 and 63 percent, respectively, in backscatter from a background stratospheric-aerosol layer at 20 km.

  9. Hygroscopic Properties of Aircraft Engine Exhaust Aerosol Produced From Traditional and Alternative Fuels

    NASA Astrophysics Data System (ADS)

    Moore, R.; Ziemba, L. D.; Beyersdorf, A. J.; Thornhill, K. L.; Winstead, E. L.; Crumeyrolle, S.; Chen, G.; Anderson, B. E.

    2012-12-01

    Aircraft emissions of greenhouse gases and aerosols constitute an important component of anthropogenic climate forcing, of which aerosol-cloud interactions remain poorly understood. It is currently thought that the ability of these aerosols to alter upper tropospheric cirrus cloud properties may produce radiative forcings many times larger than the impact of linear contrails alone and which may partially offset the impact of greenhouse gas emissions from aviation (Burkhardt and Karcher, Nature, 2011). Consequently, it is important to characterize the ability of these engine-emitted aerosol to act as cloud condensation nuclei (CCN) and ice nuclei (IN) to form clouds. While a number of studies in the literature have examined aerosol-cloud interactions for laboratory-generated soot or from aircraft engines burning traditional fuels, limited attention has been given to how switching to alternative jet fuels impacts the ability of engine-emitted aerosols to form clouds. The key to understanding these changes is the aerosol hygroscopicity. To address this need, the second NASA Alternative Aviation Fuel Experiment (AAFEX-II) was conducted in 2011 to examine the aerosol emissions from the NASA DC-8 under a variety of different engine power and fuel type conditions. Five fuel types were considered including traditional JP-8 fuel, synthetic Fischer-Tropsh (FT) fuel , sulfur-doped FT fuel (FTS) , hydrotreated renewable jet (HRJ) fuel, and a 50:50 blend of JP-8 with HRJ. Emissions were sampled from the DC-8 on the airport jetway at a distance of 145 meters downwind of the engine by a comprehensive suite of aerosol instrumentation that provided information on the aerosol concentration, size distribution, soot mass, and CCN activity. Concurrent measurements of carbon dioxide were used to account for plume dilution so that characteristic emissions indices could be determined. It is found that both engine power and fuel type significantly influence the hygroscopic properties of

  10. Sensitivity of spectral reflectance to aerosol optical properties in UV and visible wavelength range: Preparatory study for aerosol retrieval from Geostationary Environmental Monitoring Spectrometer (GEMS)

    NASA Astrophysics Data System (ADS)

    KIM, M.; Kim, J.; Lee, J.

    2011-12-01

    Asia, with its rapid increase in industrialization and population, has been receiving great attention as one of important source regions of pollutants including aerosols and trace gases. Since the spatio-temporal distribution of the pollutants varies rapidly, demands to monitor air quality in a geostationary satellite have increased recently. In these perspectives, the Ministry of Environment of Korea initiated a geostationary satellite mission to launch the Geostationary Environmental Monitoring Spectrometer (GEMS) onboard the GEO-KOMPSAT in 2017-2018 timeframe. From the Ozone Monitoring Instrument (OMI) measurements, it has been found that the low surface reflectance and strong interaction between aerosol absorption and molecular scattering in UV wavelength range can be advantageous in retrieving aerosol optical properties, such as aerosol optical thickness (AOT) and optical type (or single scattering albedo), over the source regions as well as ocean areas. In addition, GEMS is expected to have finer spatial resolution compared to OMI (13 x 24 km2 at nadir), thereby less affected by sub-pixel clouds. In this study, we present sensitivity of spectral reflectance to aerosol optical properties in ultraviolet (UV) and visible wavelength range for a purpose to retrieve aerosol optical properties from GEMS. The so called UV-VIS algorithm plans to use spectral reflectance in 350-650 nm. The algorithm retrieves AOT and aerosol type using an inversion method, which adopts pre-calculated lookup table (LUT) for a set of assumed aerosol models. For the aerosol models optimized in Asia areas, the inversion data of Aerosol Robotic Network (AERONET) located in the target areas are selectively used to archive aerosol optical properties. As a result, major aerosol types representing dust, polluted dust, and absorbing/non-absorbing anthropogenic aerosols are constructed and used for the LUT calculations. We analyze the effect of cloud contamination on the retrieved AOT by

  11. Aerosol optical properties and types over the tropical urban region of Hyderabad, India

    NASA Astrophysics Data System (ADS)

    Kharol, Shailesh Kumar; Kaskaoutis, D. G.; Rani Sharma, Anu; Kvs, Badarinath; Kambezidis, H. D.

    India is densely populated, industrialized and in the recent years has witnessed an impressive economic development. Aerosols over and around India not only affect the Indian monsoon but also the global climate. The growing population coupled with revolution in industry has resulted in higher demands for energy and transport. With more and more urbanization the usage pattern of fossil and bio-fuels are leading to changes in aerosol properties, which may cause changes in precipitation and can decelerate the hydrological cycle. Over urban areas of India aerosol emissions from fossil fuels such as coal, petrol and diesel oil dominate. Further-more, the Indian subcontinent exhibits different land characteristics ranging from vegetated areas and forests to semiarid and arid environments and tall mountains. India experiences large seasonal climatic variations, which result in extreme temperatures, rainfall and relative humidity. These meteorological and climatic features introduce large variabilities in aerosol op-tical and physico-chemical characteristics at spatial and temporal scales. In the present study, seasonal variations in aerosol properties and types were analysed over tropical urban region of Hyderabad, India during October 2007-September 2008 using MICROTOPS II sun photometer measurements. Higher aerosol optical depth (AOD) values are observed in premonsoon, while the variability of the ˚ngstrüm exponent (α) seems to be more pronounced with higher values A in winter and premonsoon and lower in the monsoon periods. The AOD at 500 nm (AOD500 ) is very large over Hyderabad, varying from 0.46±0.17 in postmonsoon to 0.65±0.22 in premon-soon periods. A discrimination of the different aerosol types over Hyderabad is also attempted using values of AOD500 and α380-870. Such discrimination is rather difficult to interpret since a single aerosol type can partly be identified only under specific conditions (e.g. anthropogenic emissions, biomass burning or dust

  12. Measurements of Hygroscopicity- and Size-Resolved Sea Spray Aerosol

    NASA Astrophysics Data System (ADS)

    Phillips, B.; Dawson, K. W.; Royalty, T. M.; Reed, R. E.; Petters, M.; Meskhidze, N.

    2015-12-01

    Atmospheric aerosols play a central role in many environmental processes by influencing the Earth's radiative balance, tropospheric chemistry, clouds, biogeochemical cycles, and visibility as well as adversely impacting human health. Based on their origin, atmospheric aerosols can be defined as anthropogenic or natural. Recent studies have shown that a large fraction of uncertainty in the radiative effects of anthropogenic aerosols is related to uncertainty in natural—background—aerosols. Marine aerosols are of particular interest due to the abundance of oceans covering the Earth's surface. Despite their importance, limited information is currently available for size- and composition-resolved marine aerosol emission fluxes. Our group has designed and built an instrument for measuring the size- and hygroscopicity-resolved sea spray aerosol fluxes. The instrument was first deployed during spring 2015 at the end of the 560 m pier of the US Army Corps of Engineers' Field Research Facility in Duck, NC. Measurements include 200 nm-sized diameter growth factor (hygroscopicity) distributions, sea spray particle flux measurements, and total sub-micron sized aerosol concentration. Ancillary ocean data includes salinity, pH, sea surface temperature, dissolved oxygen content, and relative fluorescence (proxy for [Chl-a]). Hygroscopicity distribution measurements show two broad peaks, one indicative of organics and sulfates and another suggestive of sea salt. The fraction of 200 nm-sized salt particles having hygroscopicity similar to that of sea-spray aerosol contributes up to ~24% of the distribution on days with high-speed onshore winds and up to ~3% on calm days with winds blowing from the continent. However, the total concentration of sea-spray-like particles originating from offshore versus onshore winds was relatively similar. Changes in the relative contribution of sea-salt to number concentration were caused by a concomitant changes in total aerosol concentration

  13. Measurements of aerosol chemical composition in boreal forest summer conditions

    NASA Astrophysics Data System (ADS)

    ńijälä, M.; Junninen, H.; Ehn, M.; Petäjä, T.; Vogel, A.; Hoffmann, T.; Corrigan, A.; Russell, L.; Makkonen, U.; Virkkula, A.; Mäntykenttä, J.; Kulmala, M.; Worsnop, D.

    2012-04-01

    Boreal forests are an important biome, covering vast areas of the northern hemisphere and affecting the global climate change via various feedbacks [1]. Despite having relatively few anthropogenic primary aerosol sources, they always contain a non-negligible aerosol population [2]. This study describes aerosol chemical composition measurements using Aerodyne Aerosol Mass Spectrometer (C-ToF AMS, [3]), carried out at a boreal forest area in Hyytiälä, Southern Finland. The site, Helsinki University SMEAR II measurement station [4], is situated at a homogeneous Scots pine (Pinus sylvestris) forest stand. In addition to the station's permanent aerosol, gas phase and meteorological instruments, during the HUMPPA (Hyytiälä United Measurements of Photochemistry and Particles in Air) campaign in July 2010, a very comprehensive set of atmospheric chemistry measurement instrumentation was provided by the Max Planck Institute for chemistry, Johannes Gutenberg-University, University of California and the Finnish Meteorological institute. In this study aerosol chemical composition measurements from the campaign are presented. The dominant aerosol chemical species during the campaign were the organics, although periods with elevated amounts of particulate sulfates were also seen. The overall AMS measured particle mass concentrations varied from near zero to 27 μg/m observed during a forest fire smoke episode. The AMS measured aerosol mass loadings were found to agree well with DMPS derived mass concentrations (r2=0.998). The AMS data was also compared with three other aerosol instruments. The Marga instrument [5] was used to provide a quantitative semi-online measurement of inorganic chemical compounds in particle phase. Fourier Transform Infrared Spectroscopy (FTIR) analysis was performed on daily filter samples, enabling the identification and quantification of organic aerosol subspecies. Finally an Atmospheric Pressure Chemical Ionization Ion Trap Mass Spectrometer (APCI

  14. Observed correlations between aerosol and cloud properties in an Indian Ocean trade cumulus regime

    NASA Astrophysics Data System (ADS)

    Pistone, Kristina; Praveen, Puppala S.; Thomas, Rick M.; Ramanathan, Veerabhadran; Wilcox, Eric M.; Bender, Frida A.-M.

    2016-04-01

    There are many contributing factors which determine the micro- and macrophysical properties of clouds, including atmospheric vertical structure, dominant meteorological conditions, and aerosol concentration, all of which may be coupled to one another. In the quest to determine aerosol effects on clouds, these potential relationships must be understood. Here we describe several observed correlations between aerosol conditions and cloud and atmospheric properties in the Indian Ocean winter monsoon season.In the CARDEX (Cloud, Aerosol, Radiative forcing, Dynamics EXperiment) field campaign conducted in February and March 2012 in the northern Indian Ocean, continuous measurements were made of atmospheric precipitable water vapor (PWV) and the liquid water path (LWP) of trade cumulus clouds, concurrent with measurements of water vapor flux, cloud and aerosol vertical profiles, meteorological data, and surface and total-column aerosol from instrumentation at a ground observatory and on small unmanned aircraft. We present observations which indicate a positive correlation between aerosol and cloud LWP only when considering cases with low atmospheric water vapor (PWV < 40 kg m-2), a criterion which acts to filter the data to control for the natural meteorological variability in the region.We then use the aircraft and ground-based measurements to explore possible mechanisms behind this observed aerosol-LWP correlation. The increase in cloud liquid water is found to coincide with a lowering of the cloud base, which is itself attributable to increased boundary layer humidity in polluted conditions. High pollution is found to correlate with both higher temperatures and higher humidity measured throughout the boundary layer. A large-scale analysis, using satellite observations and meteorological reanalysis, corroborates these covariations: high-pollution cases are shown to originate as a highly polluted boundary layer air mass approaching the observatory from a northwesterly

  15. Aerosol and gas re-distribution by shallow cumulus clouds: An investigation using airborne measurements

    NASA Astrophysics Data System (ADS)

    Wonaschuetz, Anna; Sorooshian, Armin; Ervens, Barbara; Chuang, Patrick Y.; Feingold, Graham; Murphy, Shane M.; de Gouw, Joost; Warneke, Carsten; Jonsson, Haflidi H.

    2012-09-01

    Aircraft measurements during the 2006 Gulf of Mexico Atmospheric Composition and Climate Study (GoMACCS) are used to examine the influence of shallow cumulus clouds on vertical profiles of aerosol chemical composition, size distributions, and secondary aerosol precursor gases. The data show signatures of convective transport of particles, gases and moisture from near the surface to higher altitudes, and of aqueous-phase production of aerosol mass (sulfate and organics) in cloud droplets and aerosol water. In cloudy conditions, the average aerosol volume concentration at an altitude of 2850 m, above typical cloud top levels, was found to be 34% of that at 450 m; for clear conditions, the same ratio was 13%. Both organic and sulfate mass fractions were on average constant with altitude (around 50%); however, the ratio of oxalate to organic mass increased with altitude (from 1% at 450 m to almost 9% at 3450 m), indicative of the influence of in-cloud production on the vertical abundance and characteristics of secondary organic aerosol (SOA) mass. A new metric termed "residual cloud fraction" is introduced as a way of quantifying the "cloud processing history" of an air parcel. Results of a parcel model simulating aqueous phase production of sulfate and organics reproduce observed trends and point at a potentially important role of SOA production, especially oligomers, in deliquesced aerosols. The observations emphasize the importance of shallow cumulus clouds in altering the vertical distribution of aerosol properties that influence both their direct and indirect effect on climate.

  16. Comparison of Modeled Backscatter using Measured Aerosol Microphysics with Focused CW Lidar Data over Pacific

    NASA Technical Reports Server (NTRS)

    Srivastava, Vandana; Clarke, Antony D.; Jarzembski, Maurice A.; Rothermel, Jeffry

    1997-01-01

    During NASA's GLObal Backscatter Experiment (GLOBE) II flight mission over the Pacific Ocean in May-June 1990, extensive aerosol backscatter data sets from two continuous wave, focused CO2 Doppler lidars and an aerosol microphysics data set from a laser optical particle counter (LOPC) were obtained. Changes in aerosol loading in various air masses with associated changes in chemical composition, from sulfuric acid and sulfates to dustlike crustal material, significantly affected aerosol backscatter, causing variation of about 3 to 4 orders of magnitude. Some of the significant backscatter features encountered in different air masses were the low backscatter in subtropical air with even lower values in the tropics near the Intertropical Convergence Zone (ITCZ), highly variable backscatter in the ITCZ, mid-tropospheric aerosol backscatter background mode, and high backscatter in an Asian dust plume off the Japanese coast. Differences in aerosol composition and backscatter for northern and southern hemisphere also were observed. Using the LOPC measurements of physical and chemical aerosol properties, we determined the complex refractive index from three different aerosol mixture models to calculate backscatter. These values provided a well-defined envelope of modeled backscatter for various atmospheric conditions, giving good agreement with the lidar data over a horizontal sampling of approximately 18000 km in the mid-troposphere.

  17. Measurements and Modeling of Aerosol Absorption and Single Scattering Albedo at Ambient Relative Hum

    NASA Technical Reports Server (NTRS)

    Redemann, J.; Russell, P. B.; Hamill, P.

    2000-01-01

    Uncertainties in the aerosol single scattering albedo have been identified to be an important source of errors in current large-scale model estimates of the direct aerosol radiative forcing of climate. A number of investigators have obtained estimates of the single scattering albedo from a variety of remote sensing and in situ measurements during aerosol field experiments. During the Tropospheric Aerosol Radiative Forcing Observational Experiment (TARFOX, 1996) for example, estimates of the aerosol single scattering albedo were obtained (1) as a best-fit parameter in comparing radiative flux changes measured by airborne pyranometer to those computed from independently measured aerosol properties; (2) from estimates of the aerosol complex index of refraction derived using a combination of airborne sunphotometer, lidar backscatter and in situ size distribution measurements; and (3) from airborne measurements of aerosol scattering and absorption using nephelometers and absorption photometers. In this paper, we briefly compare the results of the latter two methods for two TARFOX case studies, since those techniques provide height-resolved information about the aerosol single scattering albedo. Estimates of the aerosol single scattering albedo from nephelometer and absorption photometer measurements require knowledge of the scattering and absorption humidification (i.e., the increase in these properties in response to an increase in ambient relative humidity), since both measurements are usually carried out at a relative humidity different from the ambient atmosphere. In principle, the scattering humidification factor can be measured, but there is currently no technique widely available to measure the absorption of an aerosol sample as a function of relative humidity. Frequently, for lack of better knowledge, the absorption humidification is assumed to be unity (meaning that there is no change in aerosol absorption due to an increase in ambient relative humidity). This

  18. Aerosol Radiative Forcing Derived From SeaWIFS - Retrieved Aerosol Optical Properties

    NASA Technical Reports Server (NTRS)

    Chou, Mong-Dah; Chan, Pui-King; Wang, Menghua; Einaudi, Franco (Technical Monitor)

    2000-01-01

    To understand climatic implications of aerosols over global oceans, the aerosol optical properties retrieved from the Sea-viewing Wide Field-of-view Sensor (SeaWiFS) are analyzed, and the effects of the aerosols on the Earth's radiation budgets (aerosol radiative forcing, ARF) are computed using a radiative transfer model. It is found that the distribution of the SeaWiFS-retrieved aerosol optical thickness is distinctively zonal. The maximum in the equatorial region coincides with the Intertropical Convergence Zone, and the maximum in the Southern Hemispheric high latitudes coincides with the region of prevailing westerlies. The minimum aerosol optical thickness is found in the subtropical high pressure regions, especially in the Southern Hemisphere. These zonal patterns clearly demonstrate the influence of atmospheric circulation on the oceanic aerosol distribution. Over global oceans, aerosols reduce the annual mean net downward solar flux by 5.4 W m-2 at the top of the atmosphere and by 6.1 W m-2 at the surface. The largest ARF is found in the tropical Atlantic, Arabian Sea, Bay of Bengal, the coastal regions of Southeast and East Asia, and the Southern Hemispheric high latitudes. During the period of the Indonesian big fires (September-December 1997), the cooling due to aerosols is greater than 15 W m-2 at the top of the atmosphere and greater than 30 W m(exp -1) at the surface in the vicinity of the maritime continents. The atmosphere receives extra solar radiation by greater than 15 W m(exp -1) over a large area. These large changes in radiative fluxes are expected to have enhanced the atmospheric stability, weakened the atmospheric circulation, and augmented the drought condition during that period. It would be very instructive to simulate the regional climatic. The model-calculated clear sky solar flux at the top of the atmosphere is compared with that derived from the Clouds and the Earth's Radiant Energy System (CERES). The net downward solar flux of

  19. Aerosol Properties and Radiative Forcing over Kanpur during Severe Aerosol Loading Conditions

    SciTech Connect

    Kaskaoutis, D. G.; Sinha, P. R.; Vinoj, V.; Kosmopoulos, P. G.; Tripathi, S. N.; Misra, Amit; Sharma, M.; Singh, R. P.

    2013-11-01

    Atmospheric aerosols over India exhibit large spatio-temporal fluctuation driven by the local monsoon system, emission rates and seasonally-changed air masses. The northern part of India is well-known for its high aerosol loading throughout the year due to anthropogenic emissions, dust influence and biomass burning. On certain circumstances and, under favorable weather conditions, the aerosol load can be severe, causing significant health concerns and climate implications. The present work analyzes the aerosol episode (AE) days and examines the modification in aerosol properties and radiative forcing during the period 2001-2010 based on Kanpur-AERONET sun photometer data. As AEs are considered the days having daily-mean aerosol optical depth (AOD) above the decadal mean + 1 STD (standard deviation); the threshold value is defined at 0.928. The results identify 277 out of 2095 days (13.2%) of AEs over Kanpur, which are most frequently observed during post-monsoon (78 cases, 18.6%) and monsoon (76, 14.7%) seasons due to biomass-burning episodes and dust influence, respectively. On the other hand, the AEs in winter and pre-monsoon are lower in both absolute and percentage values (65, 12.5% and 58, 9.1%, respectively). The modification in aerosol properties on the AE days is strongly related to season. Thus, in post-monsoon and winter the AEs are associated with enhanced presence of fine-mode aerosols and Black Carbon from anthropogenic pollution and any kind of burning, while in pre-monsoon and monsoon seasons they are mostly associated with transported dust. Aerosol radiative forcing (ARF) calculated using SBDART shows much more surface (~-69 to -97 Wm-2) and Top of Atmosphere cooling (-20 to -30 Wm-2) as well as atmospheric heating (~43 to 71 Wm-2) during the AE days compared to seasonal means. These forcing values are mainly controlled by the higher AODs and the modified aerosol characteristics (Angstrom α, SSA) during the AE days in each season and may cause

  20. Ground Based Aerosol Measurements: Applications, Methods and Plans

    NASA Astrophysics Data System (ADS)

    Hume, E. E.; Cahill, C. F.; Carr, S. S.

    2004-05-01

    Anthropogenic and naturally occurring aerosols are linked to visibility degradation, changes in the earth's radiative balance, human health issues, acid rain, and the introduction of pollutants and/or nutrients to sensitive ecosystems. Understanding aerosols requires knowledge of the chemical constituents, sizes, the location and strength of sources, and the transport of the generated aerosols. Remote sensing techniques are used to study aerosols on large scales but are unable to retrieve the exact size distributions and chemical compositions of the observed aerosols. In situ measurements are required to interpret and understand the remotely sensed data. Details of a developing program for in situ aerosol measurement will be presented. A brief description of new aerosol sampling equipment being acquired for use in field campaigns will be given. The equipment being acquired for field campaigns are improved 8-stage rotating drum impactors designed and manufactured at the University of California, Davis. Results from previous measurement programs involving similar instruments will be presented to illustrate how these data can be utilized. Initial plans for using the instruments in measurement campaigns will be discussed.

  1. Aerosol Optical Properties over the Oceans: Summary and Interpretation of Shadow-Band Radiometer Data from Six Cruises. Chapter 19

    NASA Technical Reports Server (NTRS)

    Miller, Mark A.; Reynolds, R. M.; Bartholomew, Mary Jane

    2001-01-01

    The aerosol scattering component of the total radiance measured at the detectors of ocean color satellites is determined with atmospheric correction algorithms. These algorithms are based on aerosol optical thickness measurements made in two channels that lie in the near-infrared portion of the electromagnetic spectrum. The aerosol properties in the near-infrared region are used because there is no significant contribution to the satellite-measured radiance from the underlying ocean surface in that spectral region. In the visible wavelength bands, the spectrum of radiation scattered from the turbid atmosphere is convolved with the spectrum of radiation scattered from the surface layers of the ocean. The radiance contribution made by aerosols in the visible bands is determined from the near-infrared measurements through the use of aerosol models and radiation transfer codes. Selection of appropriate aerosol models from the near-infrared measurements is a fundamental challenge. There are several challenges with respect to the development, improvement, and evaluation of satellite ocean-color atmospheric correction algorithms. A common thread among these challenges is the lack of over-ocean aerosol data. Until recently, one of the most important limitations has been the lack of techniques and instruments to make aerosol measurements at sea. There has been steady progress in this area over the past five years, and there are several new and promising devices and techniques for data collection. The development of new instruments and the collection of more aerosol data from over the world's oceans have brought the realization that aerosol measurements that can be directly compared with aerosol measurements from ocean color satellite measurements are difficult to obtain. There are two problems that limit these types of comparisons: the cloudiness of the atmosphere over the world's oceans and the limitations of the techniques and instruments used to collect aerosol data from

  2. Retrieval Of Stratospheric Aerosol Properties From Sciamachy Limb Observations

    NASA Astrophysics Data System (ADS)

    Dorner, Steffen; Pukite, Janis; Kuhl, Sven; Penning de Vries, Marloes; Wagner, Thomas

    2013-12-01

    In this study we present a new technique to retrieve aerosol extinction profiles from SCIAMACHY measurements in limb geometry using the Monte Carlo Atmospheric Radiative Transfer Inversion Model (McArtim). Our retrieval algorithm follows the Onion-Peeling approach: Starting at a reference tan- gent height the aerosol extinction is varied for each subsequent tangent height until the simulated intensity profile is in agreement with the measurement. In self validation studies the retrieval algorithm performed well showing errors below 5 % for an altitude range of 13 to 30 km. In addition we investigated the effect of gradients in aerosol extinction along the line of sight. Using the standard homogeneous approach for aerosol plumes can lead to strong underestimations in extinction and plume altitude.

  3. Aerosol optical properties over the midcontinental United States

    SciTech Connect

    Halthore, R.N. ); Markham, B.L.; Ferrare, R.A. ); Aro, T.O. )

    1992-11-30

    This work is part of the First International Satellite Land Surface Climatology Project (ISLSCP) Field Experiment (FIFE), an international land-surface-atmosphere experiment aimed at improving the way climate models represent energy, water, heat, and carbon exchanges, and improving the utilization of satellite based remote sensing to monitor such parameters. Here the authors report on measurements of aerosol optical depth over the FIFE site, making use of a calibrated Sun photometer. Aerosols are relevant for the impact they have on remotely sensed measurements of radiation effects on the earth. They also play a major role in cloud formation, and can impact the atmospheric concentration of minor species gases. Here the authors look at the meteorological effects on aerosols in the troposphere. Wavelength dependence gives information on the size distributions within the aerosols. During 1987 they observe mixing of gulf air with continental air over the site. They report on correlation with surface values of pressure, temperature, specific, and relative humidity.

  4. Aerosol particle properties in a South American megacity

    NASA Astrophysics Data System (ADS)

    Ulke, Ana; Torres-Brizuela, Marcela; Raga, Graciela; Baumgardner, Darrel; Cancelada, Marcela

    2015-04-01

    The subtropical city of Buenos Aires is located on the western shore of Río de la Plata, on the southeastern coast of Argentina. It is the second largest metropolitan area in South America, with a population density of around 14 thousand people per km2. When all 24 counties of the Great Buenos Aires Metropolitan Area are included it is the third-largest conurbation in Latin America, with a population of around fifteen million inhabitants. The generalized worldwide trend to concentrate human activities in urban regions that continue to expand in area, threatens the local and regional environment. Air pollution in the Buenos Aires airshed is due to local sources (mainly the mobile sources, followed by the electric power plants and some industries) and to distant sources (like biomass burning, dust, marine aerosols and occasionally volcanic ash) whose products arrive in the city area due to the regional transport patterns. Previous research suggests that ambient aerosol particle concentrations should be considered an air quality problem. A field campaign was conducted in Buenos Aires in 2011 in order to characterize some aerosol particles properties measured for the first time in the city. Measurements began in mid- April and continued until December. The field observations were done in a collaborative effort between the Universities of Mexico (UNAM) and Buenos Aires (UBA). A suite of instruments was installed on the roof of an UBA laboratory and classroom buildings (34.54° S, 58.44° W) at an altitude of approximately 30 m above sea level. The measurements included the number concentration of condensation nuclei (CN) larger than approximately 50 nm, the mass concentration of particle-bound polycyclic aromatic hydrocarbons (PPAH), the scattering (Bscat) and absorption (Babs) coefficients at 550 nm and the vertical profiles of backscattered light from aerosols at a wavelength of 910 nm using a ceilometer. In addition, a weather station recorded the meteorological

  5. Airborne observations of aerosol microphysical properties and particle ageing processes in the troposphere above Europe

    NASA Astrophysics Data System (ADS)

    Hamburger, T.; McMeeking, G.; Minikin, A.; Petzold, A.; Coe, H.; Krejci, R.

    2012-08-01

    In-situ measurements of aerosol microphysical properties were performed in May 2008 during the EUCAARI-LONGREX campaign. Two aircraft, the FAAM BAe-146 and DLR Falcon 20, operated from Oberpfaffenhofen, Germany. A comprehensive data set was obtained comprising the wider region of Europe north of the Alps throughout the whole tropospheric column. Prevailing stable synoptic conditions enabled measurements of accumulating emissions inside the continental boundary layer reaching a maximum total number concentration of 19 000 particles cm-3 stp. Nucleation events were observed within the boundary layer during high pressure conditions and after updraft of emissions induced by frontal passages above 8 km altitude in the upper free troposphere. Aerosol ageing processes during air mass transport are analysed using trajectory analysis. The ratio of particles containing a non-volatile core (250 °C) to the total aerosol number concentration was observed to increase within the first 12 to 48 h from the particle source from 50 to 85% due to coagulation. Aged aerosol also features an increased fraction of accumulation mode particles of approximately 40% of the total number concentration. The presented analysis provides an extensive data set of tropospheric aerosol microphysical properties on a continental scale which can be used for atmospheric aerosol models and comparisons of satellite retrievals.

  6. Airborne observations of aerosol microphysical properties and particle ageing processes in the troposphere above Europe

    NASA Astrophysics Data System (ADS)

    Hamburger, T.; McMeeking, G.; Minikin, A.; Petzold, A.; Coe, H.; Krejci, R.

    2012-12-01

    In-situ measurements of aerosol microphysical properties were performed in May 2008 during the EUCAARI-LONGREX campaign. Two aircraft, the FAAM BAe-146 and DLR Falcon 20, operated from Oberpfaffenhofen, Germany. A comprehensive data set was obtained comprising the wider region of Europe north of the Alps throughout the whole tropospheric column. Prevailing stable synoptic conditions enabled measurements of accumulating emissions inside the continental boundary layer reaching a maximum total number concentration of 19 000 particles cm-3 stp. Ultra-fine particles as indicators for nucleation events were observed within the boundary layer during high pressure conditions and after updraft of emissions induced by frontal passages above 8 km altitude in the upper free troposphere. Aerosol ageing processes during air mass transport are analysed using trajectory analysis. The ratio of particles containing a non-volatile core (250 °C) to the total aerosol number concentration was observed to increase within the first 12 to 48 h from the particle source from 50 to 85% due to coagulation. Aged aerosol also features an increased fraction of accumulation mode particles of approximately 40% of the total number concentration. The presented analysis provides an extensive data set of tropospheric aerosol microphysical properties on a continental scale which can be used for atmospheric aerosol models and comparisons of satellite retrievals.

  7. A balloon-borne aerosol spectrometer for high altitude low aerosol concentration measurements

    SciTech Connect

    Brown, G.S. ); Weiss, R.E. )

    1990-08-01

    Funded by Air Force Wright Aeronautical Laboratory, a new balloon-borne high altitude aerosol spectrometer, for the measurement of cirrus cloud ice crystals, has been developed and successfully flown by Sandia National Laboratories and Radiance Research. This report (1) details the aerosol spectrometer design and construction, (2) discusses data transmission and decoding, (3) presents data collected on three Florida flights in tables and plots. 2 refs., 11 figs., 3 tabs.

  8. Observed changes in aerosol physical and optical properties before and after precipitation events

    NASA Astrophysics Data System (ADS)

    Li, Xingmin; Dong, Yan; Dong, Zipeng; Du, Chuanli; Chen, Chuang

    2016-08-01

    Precipitation scavenging of aerosol particles is an important removal process in the atmosphere that can change aerosol physical and optical properties. This paper analyzes the changes in aerosol physical and optical properties before and after four rain events using in situ observations of mass concentration, number concentration, particle size distribution, scattering and absorption coefficients of aerosols in June and July 2013 at the Xianghe comprehensive atmospheric observation station in China. The results show the effect of rain scavenging is related to the rain intensity and duration, the wind speed and direction. During the rain events, the temporal variation of aerosol number concentration was consistent with the variation in mass concentration, but their size-resolved scavenging ratios were different. After the rain events, the increase in aerosol mass concentration began with an increase in particles with diameter <0.8 μm [measured using an aerodynamic particle sizer (APS)], and fine particles with diameter <0.1 μm [measured using a scanning mobility particle sizer (SMPS)]. Rainfall was most efficient at removing particles with diameter ~0.6 μm and greater than 3.5 μm. The changes in peak values of the particle number distribution (measured using the SMPS) before and after the rain events reflect the strong scavenging effect on particles within the 100-120 nm size range. The variation patterns of aerosol scattering and absorption coefficients before and after the rain events were similar, but their scavenging ratios differed, which may have been related to the aerosol particle size distribution and chemical composition.

  9. Providing Size-Resolved Mixing State Inputs to Improve Aerosol Optics Models: Comparison of ACE-Asia Aerosol Chemical Measurements for Different Source Regions With Simultaneous Optical Measurements

    NASA Astrophysics Data System (ADS)

    Sullivan, R. C.; Poon, G.; Guazzotti, S.; Sodeman, D.; Holecek, J.; Spencer, M.; Prather, K.

    2005-12-01

    Measurements made of the aerodynamic size and chemical composition of single aerosol particles on board the R/V Ronald H. Brown sailing between Hawaii and the Sea of Japan during ACE-Asia in 2001 revealed a complex mixture of mineral dust, organic carbon, elemental carbon, sulfates, nitrates, chloride, ammonium, and sea salt. The air mass source regions included influences from the Pacific Ocean, Miyakejima volcano, Gobi and Taklimakan Deserts, Shanghai, Japan, and Korea. The particle composition sampled from each of these regions showed unique changes in the aerosol's mixing state. This complexity presents major challenges in accurately modeling the optical properties of the Asian aerosol. The degree of closure between the measured chemical and optical properties of this aerosol and those predicted by models has been presented by Quinn et al. [JGR, 109, D19S01, doi: 10.1029/2003JD004010, 2004]. Differences between measured and calculated aerosol absorption coefficients were partly attributed to the assumption of internally mixed homogeneous spheres for the aerosol population. Good correlations between measured and calculated aerosol mass and light scattering were found but relied on particle shapes not confirmed by measurements. To better our understanding of the relationship between aerosol chemistry and optical measurements, and provide more detailed inputs to improve the predictions of optical models, we present size-resolved single-particle mixing state results obtained by an ATOFMS for the seven air mass source regions described by Quinn et al. (2004). Our results do not support the assumption of a homogeneous internally mixed aerosol population for many of the source regions. Particular focus is given to the mixing state and chemical associations of sulfate, nitrate, chloride, ammonium, OC, EC, dust, and sea salt. We demonstrate the segregation of ammonium, sulfate, and nitrate within individual particles throughout the study and discuss the different

  10. Ground-based remote sensing of aerosol climatology in China: Aerosol optical properties, direct radiative effect and its parameterization

    NASA Astrophysics Data System (ADS)

    Xia, X.; Che, H.; Zhu, J.; Chen, H.; Cong, Z.; Deng, X.; Fan, X.; Fu, Y.; Goloub, P.; Jiang, H.; Liu, Q.; Mai, B.; Wang, P.; Wu, Y.; Zhang, J.; Zhang, R.; Zhang, X.

    2016-01-01

    Spatio-temporal variation of aerosol optical properties and aerosol direct radiative effects (ADRE) are studied based on high quality aerosol data at 21 sunphotometer stations with at least 4-months worth of measurements in China mainland and Hong Kong. A parameterization is proposed to describe the relationship of ADREs to aerosol optical depth at 550 nm (AOD) and single scattering albedo at 550 nm (SSA). In the middle-east and south China, the maximum AOD is always observed in the burning season, indicating a significant contribution of biomass burning to AOD. Dust