WorldWideScience

Sample records for satellite stratospheric aerosol

  1. Stratospheric Aerosol Measurements

    Science.gov (United States)

    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

  2. Variation in the stratospheric aerosol associated with the North Cyclonic Polar Vortex as measured by the SAM II satellite sensor. [Stratospheric Aerosol Measurement

    Science.gov (United States)

    Kent, G. S.; Farrukh, U. O.; Trepte, C. R.; Mccormick, M. P.

    1985-01-01

    Optical depth data gathered by the stratospheric aerosol measurement (SAM II) satellite during the 1979-80 winter season are analyzed to study mean atmospheric motions. The spacecraft photometer yielded extinction rates over the Northern Hemisphere in the 8-30 km altitude interval. Filtering was performed to remove the effects of high clouds and polar stratospheric clouds. Free horizontal mixing was prevalent below 14 km, as was a systematic difference across the polar jet stream above that altitude. The aerosol declined in altitude as the winter progressed. The polar vortex is concluded to have a base at the 14 km altitude and an outer boundary which coincides with the jet stream axis. The model accords with atmospheric tracer measurements made during the open-air nuclear testing programs in the 1950s.

  3. Variability and evolution of the midlatitude stratospheric aerosol budget from 22 years of ground-based lidar and satellite observations

    Science.gov (United States)

    Khaykin, Sergey M.; Godin-Beekmann, Sophie; Keckhut, Philippe; Hauchecorne, Alain; Jumelet, Julien; Vernier, Jean-Paul; Bourassa, Adam; Degenstein, Doug A.; Rieger, Landon A.; Bingen, Christine; Vanhellemont, Filip; Robert, Charles; DeLand, Matthew; Bhartia, Pawan K.

    2017-02-01

    The article presents new high-quality continuous stratospheric aerosol observations spanning 1994-2015 at the French Observatoire de Haute-Provence (OHP, 44° N, 6° E) obtained by two independent, regularly maintained lidar systems operating within the Network for Detection of Atmospheric Composition Change (NDACC). Lidar series are compared with global-coverage observations by Stratospheric Aerosol and Gas Experiment (SAGE II), Global Ozone Monitoring by Occultation of Stars (GOMOS), Optical Spectrograph and InfraRed Imaging System (OSIRIS), Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP), and Ozone Mapping Profiling Suite (OMPS) satellite instruments, altogether covering the time span of OHP lidar measurements. Local OHP and zonal-mean satellite series of stratospheric aerosol optical depth are in excellent agreement, allowing for accurate characterization of stratospheric aerosol evolution and variability at northern midlatitudes during the last 2 decades. The combination of local and global observations is used for a careful separation between volcanically perturbed and quiescent periods. While the volcanic signatures dominate the stratospheric aerosol record, the background aerosol abundance is found to be modulated remotely by the poleward transport of convectively cleansed air from the deep tropics and aerosol-laden air from the Asian monsoon region. The annual cycle of background aerosol at midlatitudes, featuring a minimum during late spring and a maximum during late summer, correlates with that of water vapor from the Aura Microwave Limb Sounder (MLS). Observations covering two volcanically quiescent periods over the last 2 decades provide an indication of a growth in the nonvolcanic component of stratospheric aerosol. A statistically significant factor of 2 increase in nonvolcanic aerosol since 1998, seasonally restricted to late summer and fall, is associated with the influence of the Asian monsoon and growing pollution therein.

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

    Science.gov (United States)

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

    1989-01-01

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

  5. On the stratospheric aerosol budget at Northern mid-latitudes from 21 years of ground-based lidar and satellite observations

    Science.gov (United States)

    Khaykin, Sergey; Godin-Beekmann, Sophie; Hauchecorne, Alain; Vernier, Jean-Paul; Jumelet, Julien; Keckhut, Philippe

    2016-04-01

    The paper presents a new high-quality 21-year series of continuous stratospheric aerosol observations at Observatoire de Haute-Provence (OHP, 44° N, 6° E) in Southern France using two powerful and well-maintained lidar systems. In contrast to previous studies making use of the observations by aerosol-dedicated lidars operating within the Network for Detection of Atmospheric Composition Change (NDACC), we exploit the backscatter measurements from the off-line 355 nm channel of stratospheric ozone lidar (LiO3S) and low-gain 532 nm channel of stratospheric temperature lidar (LTA). The presented series of stratospheric aerosol backscatter and extinction at 532 nm, spanning from January 1994 through 2016, include on average 10-11 lidar acquisitions per month after careful quality screening. The OHP lidar observations are compared with global space-borne measurements of zonal-mean stratospheric extinction by SAGE II, GOMOS, OSIRIS and CALIOP instruments, altogether covering the time span of OHP lidar data sets. Both ground-based and satellite monthly-mean stratospheric Aerosol Optical Depth between 17 and 30 km altitude (sAOD1730km) series are in good cross-agreement with discrepancies well below the measurement errors, thereby ensuring the quality and coherency of all data sets exploited for our study. The global satellite observations are then used to identify the drivers of stratospheric aerosol variability observed locally by the OHP lidars. The 21-year aerosol series reflect two essential periods in the global volcanic activity over the past two decades. The first one, a long volcanically-quiescent period of low aerosol burden (0.002Vernier et al. (2011), takes place mainly during the southern tropics convective season, which together with the timescale of poleward transport is compatible with the observed seasonality of aerosol in the mid-latitude stratosphere.

  6. SAM-2 ground-truth plan: Correlative measurements for the Stratospheric Aerosol Measurement-2 (SAM 2) sensor on the Nimbus G satellite

    Science.gov (United States)

    Russell, P. B.; Mccormick, M. P.; Mcmaster, L. R.; Pepin, T. J.; Chu, W. P.; Swissler, T. J.

    1978-01-01

    The SAM-2 will fly aboard the Nimbus-G satellite for launch in the fall of 1978 and measure stratospheric vertical profiles of aerosol extinction in high latitude bands. The plan gives details of the location and times for the simultaneous satellite/correlative measurements for the nominal launch time, the rationale and choice of the correlative sensors, their characteristics and expected accuracies, and the conversion of their data to extinction profiles. The SAM-2 expected instrument performance and data inversion results are presented. Various atmospheric models representative of polar stratospheric aerosols are used in the SAM-2 and correlative sensor analyses.

  7. Stratospheric ozone depletion over Antarctica - Role of aerosols based on SAGE II satellite observations

    Science.gov (United States)

    Lin, N.-H.; Saxena, V. K.

    1992-01-01

    The physical characteristics of the Antarctic stratospheric aerosol are investigated via a comprehensive analysis of the SAGE II data during the most severe ozone depletion episode of October 1987. The aerosol size distribution is found to be bimodal in several instances using the randomized minimization search technique, which suggests that the distribution of a single mode may be used to fit the data in the retrieved size range only at the expense of resolution for the larger particles. On average, in the region below 18 km, a wavelike perturbation with the upstream tilting for the parameters of mass loading, total number, and surface area concentration is found to be located just above the region of the most severe ozone depletion.

  8. Optimal estimation retrieval of aerosol microphysical properties from SAGE II satellite observations in the volcanically unperturbed lower stratosphere

    Directory of Open Access Journals (Sweden)

    T. Deshler

    2010-05-01

    Full Text Available Stratospheric aerosol particles under non-volcanic conditions are typically smaller than 0.1 μm. Due to fundamental limitations of the scattering theory in the Rayleigh limit, these tiny particles are hard to measure by satellite instruments. As a consequence, current estimates of global aerosol properties retrieved from spectral aerosol extinction measurements tend to be strongly biased. Aerosol surface area densities, for instance, are observed to be about 40% smaller than those derived from correlative in situ measurements (Deshler et al., 2003. An accurate knowledge of the global distribution of aerosol properties is, however, essential to better understand and quantify the role they play in atmospheric chemistry, dynamics, radiation and climate. To address this need a new retrieval algorithm was developed, which employs a nonlinear Optimal Estimation (OE method to iteratively solve for the monomodal size distribution parameters which are statistically most consistent with both the satellite-measured multi-wavelength aerosol extinction data and a priori information. By thus combining spectral extinction measurements (at visible to near infrared wavelengths with prior knowledge of aerosol properties at background level, even the smallest particles are taken into account which are practically invisible to optical remote sensing instruments. The performance of the OE retrieval algorithm was assessed based on synthetic spectral extinction data generated from both monomodal and small-mode-dominant bimodal sulphuric acid aerosol size distributions. For monomodal background aerosol, the new algorithm was shown to fairly accurately retrieve the particle sizes and associated integrated properties (surface area and volume densities, even in the presence of large extinction uncertainty. The associated retrieved uncertainties are a good estimate of the true errors. In the case of bimodal background aerosol, where the retrieved (monomodal size

  9. The capability of satellite borne remote sensors to measure stratospheric trace constituents. Volume 2: Ozone and aerosol related missions

    Science.gov (United States)

    Keitz, E. L.

    1978-01-01

    Stratospheric trace constituent measurement requirements are separated into two somewhat overlapping areas. In the first area, it is assumed that the only problem of interest is ozone; its chemistry chain, environmental effects and measurement requirements. In like manner, in the second area it is assumed that the only problem of interest is stratospheric aerosols; their chemistry, effects and measurement requirements.

  10. Stratospheric aerosol geoengineering

    Energy Technology Data Exchange (ETDEWEB)

    Robock, Alan [Department of Environmental Sciences, Rutgers University, 14 College Farm Road, New Brunswick, NJ 08901 (United States)

    2015-03-30

    The Geoengineering Model Intercomparison Project, conducting climate model experiments with standard stratospheric aerosol injection scenarios, has found that insolation reduction could keep the global average temperature constant, but global average precipitation would reduce, particularly in summer monsoon regions around the world. Temperature changes would also not be uniform; the tropics would cool, but high latitudes would warm, with continuing, but reduced sea ice and ice sheet melting. Temperature extremes would still increase, but not as much as without geoengineering. If geoengineering were halted all at once, there would be rapid temperature and precipitation increases at 5–10 times the rates from gradual global warming. The prospect of geoengineering working may reduce the current drive toward reducing greenhouse gas emissions, and there are concerns about commercial or military control. Because geoengineering cannot safely address climate change, global efforts to reduce greenhouse gas emissions and to adapt are crucial to address anthropogenic global warming.

  11. Stratospheric aerosol geoengineering

    Science.gov (United States)

    Robock, Alan

    2015-03-01

    The Geoengineering Model Intercomparison Project, conducting climate model experiments with standard stratospheric aerosol injection scenarios, has found that insolation reduction could keep the global average temperature constant, but global average precipitation would reduce, particularly in summer monsoon regions around the world. Temperature changes would also not be uniform; the tropics would cool, but high latitudes would warm, with continuing, but reduced sea ice and ice sheet melting. Temperature extremes would still increase, but not as much as without geoengineering. If geoengineering were halted all at once, there would be rapid temperature and precipitation increases at 5-10 times the rates from gradual global warming. The prospect of geoengineering working may reduce the current drive toward reducing greenhouse gas emissions, and there are concerns about commercial or military control. Because geoengineering cannot safely address climate change, global efforts to reduce greenhouse gas emissions and to adapt are crucial to address anthropogenic global warming.

  12. Analysis of the sensitivity of thermal infrared nadir satellite observations to the chemical and micro-physical properties of upper tropospheric-lower stratospheric sulphate aerosols

    Science.gov (United States)

    Sellitto, Pasquale; Sèze, Geneviève; Legras, Bernard

    2015-04-01

    Secondary sulphate aerosols are the predominant typology of aerosols in the upper troposphere/lower stratosphere (UTLS), and can have an important impact on radiative transfer and climate, cirrus formation and chemistry in the UTLS. Despite their importance, the satellite observation at the regional scale of sulphate aerosols in the UTLS is limited. In this work, we address the sensitivity of the thermal infrared satellite observations to secondary sulphate aerosols in the UTLS. The absorption properties of sulphuric acid/water droplets, for different sulphuric acid mixing ratios and temperatures, are systematically analysed. The absorption coefficients are derived by means of a Mie code, using refractive indexes taken from the GEISA (Gestion et Etude des Informations Spectroscopiques Atmosphériques : Management and Study of Spectroscopic Information) spectroscopic database and log-normal size distributions with different effective radii and number concentrations. IASI (Infrared Atmospheric Sounding Interferometer) and SEVIRI (Spinning Enhanced Visible and Infrared Imager) pseudo-observations are generated using forward radiative transfer calculations performed with the 4A (Automatized Atmospheric Absorption Atlas) radiative transfer model, to estimate the impact of the absorption of idealized aerosol layers, at typical UTLS conditions, on the radiance spectra observed by these simulated satellite instruments. We found a marked spectral signature of these aerosol layers between 700 and 1200 cm-1, due to the absorption bands of the sulphate and bi-sulphate ions and the undissociated sulphuric acid, with absorption peaks at 1170 and 905 cm-1. Micro-windows with a sensitivity to chemical and micro-physical properties of the sulphate aerosol layer are identified, and the role of interfering species, and temperature and water vapour profile is discussed.

  13. Atmospheric responses to stratospheric aerosol geoengineering

    Science.gov (United States)

    Ferraro, Angus; Highwood, Eleanor; Charlton-Perez, Andrew

    2013-04-01

    Stratospheric aerosol geoengineering, also called solar radiation management (SRM), involves the injection of aerosol into the stratosphere to increase the planetary albedo. It has been conceieved as a policy option in response to human-induced global warming. It is well-established from modelling studies and observations following volcanic eruptions that stratospheric sulphate aerosols cause global cooling. Some aspects of the climate response, especially those involving large-scale dynamical changes, are more uncertain. This work attempts to identify the physical mechanisms operating in the climate response to stratospheric aerosol geoengineering using idealised model experiments. The radiative forcing produced by the aerosol depends on its type (species) and size. Aerosols absorb terrestrial and solar radiation, which drives stratospheric temperature change. The stratospheric temperature change also depends on aerosol type and size. We calculate the stratospheric temperature change due to geoengineering with sulphate, titania, limestone and soot in a fixed-dynamical-heating radiative model. Sulphate produces tropical heating of up to ~6 K. Titania produces much less heating, whereas soot produces much more. Most aerosols increase the meridional temperature gradient in the lower stratosphere which, by thermal wind balance, would be expected to intensify the zonal winds in the polar vortex. An intermediate-complexity general circulation model is used to investigate the dynamical response to geoengineering aerosols. Atmospheric carbon dioxide concentrations are quadrupled. The carbon dioxide forcing is then balanced using stratospheric sulphate aerosol. We assess dynamical changes in the stratosphere, for example, the frequency of stratospheric sudden warmings and the strength of the Brewer-Dobson overturning circulation. We also assess changes in the strength and position of the tropospheric jets. We compare results for sulphate with those for titania.

  14. Particle size distribution of the stratospheric aerosol from SCIAMACHY limb measurements

    Science.gov (United States)

    Rozanov, Alexei; Malinina, Elizaveta; Rozanov, Vladimir; Hommel, Rene; Burrows, John

    2016-04-01

    Stratospheric aerosols are of a great scientific interest because of their crucial role in the Earth's radiative budget as well as their contribution to chemical processes resulting in ozone depletion. While the permanent aerosol background in the stratosphere is determined by the tropical injection of SO2, COS and sulphate particles from the troposphere, major perturbations of the stratospheric aerosol layer result form an uplift of SO2 after strong volcanic eruptions. Satellite measurements in the visible spectral range represent one of the most important sources of information about the vertical distribution of the stratospheric aerosol on the global scale. This study employs measurements of the scattered solar light performed in the limb viewing geometry from the space borne spectrometer SCIAMACHY, which operated onboard the ENVISAT satellite, from August 2002 to April 2012. A retrieval approach to obtain parameters of the stratospheric aerosol particle size distribution will be reported along with the sensitivity studies and first results.

  15. Spectral signatures of polar stratospheric clouds and sulfate aerosol

    Energy Technology Data Exchange (ETDEWEB)

    Massie, S.T.; Bailey, P.L.; Gille, J.C. [National Center for Atmospheric Research, Boulder, CO (United States); Lee, E.C. [Princeton Univ., NJ (United States); Mergenthaler, J.L.; Roche, A.E.; Kumer, J.B. [Lockheed Palo Alto Research Lab., CA (United States); Fishbein, E.F.; Waters, J.W. [California Institute of Technology, Pasadena, CA (United States); Lahoz, W.A. [Univ. of Reading (United Kingdom)

    1994-10-15

    Multiwavelength observations of Antarctic and midlatitude aerosol by the Cryogenic Limb Array Etalon Spectrometer (CLAES) experiment on the Upper Atmosphere Research Satellite are used to demonstrate a technique that identifies the location of polar stratospheric clouds. The technique discussed uses the normalized area of the triangle formed by the aerosol extinctions at 925, 1257, and 1605 cm{sup {minus}1} (10.8, 8.0, and 6.2 {mu}m) to derive a spectral aerosol measure M of the aerosol spectrum. Mie calculations for spherical particles and T-matrix calculations for spheroidal particles are used to generate theoretical spectral extinction curves for sulfate and polar stratospheric cloud particles. The values of the spectral aerosol measure M for the sulfate and polar stratospheric cloud particles are shown to be different. Aerosol extinction data, corresponding to temperatures between 180 and 220 K at a pressure of 46 hPa (near 21-km altitude) for 18 August 1992, are used to demonstrate the technique. Thermodynamic calculations, based upon frost-point calculation and laboratory phase-equilibrium studies of nitric acid trihydrate, are used to predict the location of nitric acid trihydrate cloud particles. 47 refs., 22 figs., 3 tabs.

  16. Merging the SAGE II and OSIRIS Stratospheric Aerosol Records

    Science.gov (United States)

    Rieger, Landon; Bourassa, Adam; Degenstein, Doug

    2016-04-01

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

  17. Stratospheric Aerosol--Observations, Processes, and Impact on Climate

    Science.gov (United States)

    Kresmer, Stefanie; Thomason, Larry W.; von Hobe, Marc; Hermann, Markus; Deshler, Terry; Timmreck, Claudia; Toohey, Matthew; Stenke, Andrea; Schwarz, Joshua P.; Weigel, Ralf; Fueglistaler, Stephan; Prata, Fred J.; Vernier, Jean-Paul; Schlager, Hans; Barnes, John E.; Antuna-Marrero, Juan-Carlos; Fairlie, Duncan; Palm, Mathias; Mahieu, Emmanuel; Notholt, Justus; Rex, Markus; Bingen, Christine; Vanhellemont, Filip; Bourassa, Adam; Plane, John M. C.; Klocke, Daniel; Carn, Simon A.; Clarisse, Lieven; Trickl, Thomas; Neeley, Ryan; James, Alexander D.; Rieger, Landon; Wilson, James C.; Meland, Brian

    2016-01-01

    Interest in stratospheric aerosol and its role in climate have increased over the last decade due to the observed increase in stratospheric aerosol since 2000 and the potential for changes in the sulfur cycle induced by climate change. This review provides an overview about the advances in stratospheric aerosol research since the last comprehensive assessment of stratospheric aerosol was published in 2006. A crucial development since 2006 is the substantial improvement in the agreement between in situ and space-based inferences of stratospheric aerosol properties during volcanically quiescent periods. Furthermore, new measurement systems and techniques, both in situ and space based, have been developed for measuring physical aerosol properties with greater accuracy and for characterizing aerosol composition. However, these changes induce challenges to constructing a long-term stratospheric aerosol climatology. Currently, changes in stratospheric aerosol levels less than 20% cannot be confidently quantified. The volcanic signals tend to mask any nonvolcanically driven change, making them difficult to understand. While the role of carbonyl sulfide as a substantial and relatively constant source of stratospheric sulfur has been confirmed by new observations and model simulations, large uncertainties remain with respect to the contribution from anthropogenic sulfur dioxide emissions. New evidence has been provided that stratospheric aerosol can also contain small amounts of nonsulfatematter such as black carbon and organics. Chemistry-climate models have substantially increased in quantity and sophistication. In many models the implementation of stratospheric aerosol processes is coupled to radiation and/or stratospheric chemistry modules to account for relevant feedback processes.

  18. Atmosphere aerosol satellite project Aerosol-UA

    Science.gov (United States)

    Milinevsky, Gennadi; Yatskiv, Yaroslav; Syniavskyi, Ivan; Bovchaliuk, Andrii; Degtyaryov, Oleksandr; Sosonkin, Mikhail; Mishchenko, Michael; Danylevsky, Vassyl; Ivanov, Yury; Oberemok, Yevgeny; Masley, Volodymyr; Rosenbush, Vera; Moskalev, Sergii

    2017-04-01

    The experiment Aerosol-UA is Ukrainian space mission aimed to the terrestrial atmospheric aerosol spatial distribution and microphysics investigations. The experiment concept is based on idea of Glory/APS mission of precise orbital measurements of polarization and intensity of the sunlight scattered by the atmosphere, aerosol and the surface the multichannel Scanning Polarimeter (ScanPol) with narrow field-of-view. ScanPol measurements will be accompanied by the wide-angle MultiSpectral Imager-Polarimeter (MSIP). The ScanPol is designed to measure Stokes parameters I, Q, U within the spectral range from the UV to the SWIR in a wide range of phase angles along satellite ground path. Expected ScanPol polarimetric accuracy is 0.15%. A high accuracy measurement of the degree of linear polarization is provided by on-board calibration of the ScanPol polarimeter. On-board calibration is performed for each scan of the mirror scanning system. A set of calibrators is viewed during the part of the scan range when the ScanPol polarimeter looks in the direction opposite to the Earth's surface. These reference assemblies provide calibration of the zero of the polarimetric scale (unpolarized reference assembly) and the scale factor for the polarimetric scale (polarized reference assembly). The zero of the radiometric scale is provided by the dark reference assembly.The spectral channels of the ScanPol are used to estimate the tropospheric aerosol absorption, the aerosol over the ocean and the land surface, the signals from cirrus clouds, stratospheric aerosols caused by major volcanic eruptions, and the contribution of the Earth's surface. The imager-polarimeter MSIP will collect 60°x60° field-of-view images on the state of the atmosphere and surface in the area, where the ScanPol polarimeter will measure, to retrieve aerosol optical depth and polarization properties of aerosol by registration of three Stokes parameters simultaneously in three spectral channels. The two more

  19. The Many Problems with Geoengineering Using Stratospheric Aerosols

    Science.gov (United States)

    Robock, Alan

    2009-05-01

    In response to the global warming problem, there has been a recent renewed call for geoengineering ``solutions'' involving injecting particles into the stratosphere or blocking sunlight with satellites between the Sun and Earth. While volcanic eruptions have been suggested as innocuous examples of stratospheric aerosols cooling the planet, the volcano analog actually argues against geoengineering because of ozone depletion and regional hydrologic and temperature responses. In this talk, I consider the suggestion to create an artificial stratospheric aerosol layer. No systems to conduct geoengineering now exist, but a comparison of different proposed stratospheric injection schemes, airplanes, balloons, artillery, and a space elevator, shows that using airplanes would not be that expensive. We simulated the climate response to both tropical and Arctic stratospheric injection of sulfate aerosol precursors using a comprehensive atmosphere-ocean general circulation model, the National Aeronautics and Space Administration Goddard Institute for Space Studies ModelE. We simulated the injection of SO2 and the model converts it to sulfate aerosols, transports them and removes them through dry and wet deposition, and calculates the climate response to the radiative forcing from the aerosols. We conducted simulations of future climate with the Intergovernmental Panel on Climate Change A1B business-as-usual scenario both with and without geoengineering, and compare the results. We found that if there were a way to continuously inject SO2 into the lower stratosphere, it would produce global cooling. Acid deposition from the sulfate would not be enough to disturb most ecosystems. Tropical SO2 injection would produce sustained cooling over most of the world, with more cooling over continents. Arctic SO2 injection would not just cool the Arctic. But both tropical and Arctic SO2 injection would disrupt the Asian and African summer monsoons, reducing precipitation to the food supply

  20. The persistently variable "background" stratospheric aerosol layer and global climate change.

    Science.gov (United States)

    Solomon, S; Daniel, J S; Neely, R R; Vernier, J-P; Dutton, E G; Thomason, L W

    2011-08-12

    Recent measurements demonstrate that the "background" stratospheric aerosol layer is persistently variable rather than constant, even in the absence of major volcanic eruptions. Several independent data sets show that stratospheric aerosols have increased in abundance since 2000. Near-global satellite aerosol data imply a negative radiative forcing due to stratospheric aerosol changes over this period of about -0.1 watt per square meter, reducing the recent global warming that would otherwise have occurred. Observations from earlier periods are limited but suggest an additional negative radiative forcing of about -0.1 watt per square meter from 1960 to 1990. Climate model projections neglecting these changes would continue to overestimate the radiative forcing and global warming in coming decades if these aerosols remain present at current values or increase.

  1. Efficient transport of tropospheric aerosol into the stratosphere via the Asian summer monsoon anticyclone

    Science.gov (United States)

    Yu, Pengfei; Rosenlof, Karen H.; Liu, Shang; Telg, Hagen; Thornberry, Troy D.; Rollins, Andrew W.; Portmann, Robert W.; Bai, Zhixuan; Ray, Eric A.; Duan, Yunjun; Pan, Laura L.; Toon, Owen B.; Bian, Jianchun; Gao, Ru-Shan

    2017-07-01

    An enhanced aerosol layer near the tropopause over Asia during the June-September period of the Asian summer monsoon (ASM) was recently identified using satellite observations. Its sources and climate impact are presently not well-characterized. To improve understanding of this phenomenon, we made in situ aerosol measurements during summer 2015 from Kunming, China, then followed with a modeling study to assess the global significance. The in situ measurements revealed a robust enhancement in aerosol concentration that extended up to 2 km above the tropopause. A climate model simulation demonstrates that the abundant anthropogenic aerosol precursor emissions from Asia coupled with rapid vertical transport associated with monsoon convection leads to significant particle formation in the upper troposphere within the ASM anticyclone. These particles subsequently spread throughout the entire Northern Hemispheric (NH) lower stratosphere and contribute significantly (˜15%) to the NH stratospheric column aerosol surface area on an annual basis. This contribution is comparable to that from the sum of small volcanic eruptions in the period between 2000 and 2015. Although the ASM contribution is smaller than that from tropical upwelling (˜35%), we find that this region is about three times as efficient per unit area and time in populating the NH stratosphere with aerosol. With a substantial amount of organic and sulfur emissions in Asia, the ASM anticyclone serves as an efficient smokestack venting aerosols to the upper troposphere and lower stratosphere. As economic growth continues in Asia, the relative importance of Asian emissions to stratospheric aerosol is likely to increase.

  2. Stratospheric Aerosols for Solar Radiation Management

    Science.gov (United States)

    Kravitz, Ben

    SRM in the context of this entry involves placing a large amount of aerosols in the stratosphere to reduce the amount of solar radiation reaching the surface, thereby cooling the surface and counteracting some of the warming from anthropogenic greenhouse gases. The way this is accomplished depends on the specific aerosol used, but the basic mechanism involves backscattering and absorbing certain amounts of solar radiation aloft. Since warming from greenhouse gases is due to longwave (thermal) emission, compensating for this warming by reduction of shortwave (solar) energy is inherently imperfect, meaning SRM will have climate effects that are different from the effects of climate change. This will likely manifest in the form of regional inequalities, in that, similarly to climate change, some regions will benefit from SRM, while some will be adversely affected, viewed both in the context of present climate and a climate with high CO2 concentrations. These effects are highly dependent upon the means of SRM, including the type of aerosol to be used, the particle size and other microphysical concerns, and the methods by which the aerosol is placed in the stratosphere. SRM has never been performed, nor has deployment been tested, so the research up to this point has serious gaps. The amount of aerosols required is large enough that SRM would require a major engineering endeavor, although SRM is potentially cheap enough that it could be conducted unilaterally. Methods of governance must be in place before deployment is attempted, should deployment even be desired. Research in public policy, ethics, and economics, as well as many other disciplines, will be essential to the decision-making process. SRM is only a palliative treatment for climate change, and it is best viewed as part of a portfolio of responses, including mitigation, adaptation, and possibly CDR. At most, SRM is insurance against dangerous consequences that are directly due to increased surface air

  3. ISA-MIP: A co-ordinated intercomparison of Interactive Stratospheric Aerosol models

    Science.gov (United States)

    Timmreck, Claudia; Mann, Graham; Aquila, Valentina; Bruehl, Christoph; Chin, Mian; Dohmse, Sandip; English, Jason; Lee, Lindsay; Mills, Michael; Hommel, Rene; Neely, Ryan; Schmidt, Anja; Sheng, Jianxiong; Toohey, Matthew; Weisenstein, Debra

    2016-04-01

    The SPARC activity, "Stratospheric Sulfur and its Role in Climate" (SSiRC) was initiated to coordinate international research activities on modelling and observation of stratospheric sulphate aerosols (and precursor gases) in order to assess its climate forcing and feedback. With several international activities to extend and improve observational stratospheric aerosol capabilities and data sets, and a growing number of global models treating stratospheric aerosol interactively, a new model intercomparison activity "ISA-MIP" has been established in the frame of SSIRC. ISA-MIP will compare interactive stratospheric aerosol (ISA) models using a range of observations to constrain and improve the models and to provide a sound scientific basis for future work. Four ISA-MIP experiments have been designed to assess different periods of the obervational stratospheric aerosol record, and to explore key processes which influence the formation and temporal development of stratospheric aerosol. The "Background" experiment will focus on the role of microphysical and transport processes under volcanically quiescent conditions, where the stratospheric aerosol size distribution is only modulated by seasonal circulations. The "Model intercomparison of Transient Aerosol Record" (MiTAR) experiment will focus on addressing the role of small- to moderate-magnitude volcanic eruptions and transport processes in the upper troposphere - lower stratosphere (UTLS) aerosols loading over the period 1998-2011. Background and MiTAR simulations will be compared to recent in-situ and satellite observations to evaluate the performances of the model and understand their strengths and weaknesses. Two further experiments investigate the radiative forcing from historical major eruptions. The Historical Eruptions SO2 Emission Assessment (HErSEA) will involve models carrying out mini-ensembles of the stratospheric aerosol perturbations from each of the 1963 Agung, 1982 El Chichon and 1991 Pinatubo

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

    Science.gov (United States)

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

    2015-01-01

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

  5. Stratospheric dryness: model simulations and satellite observations

    Directory of Open Access Journals (Sweden)

    J. Lelieveld

    2007-01-01

    Full Text Available The mechanisms responsible for the extreme dryness of the stratosphere have been debated for decades. A key difficulty has been the lack of comprehensive models which are able to reproduce the observations. Here we examine results from the coupled lower-middle atmosphere chemistry general circulation model ECHAM5/MESSy1 together with satellite observations. Our model results match observed temperatures in the tropical lower stratosphere and realistically represent the seasonal and inter-annual variability of water vapor. The model reproduces the very low water vapor mixing ratios (below 2 ppmv periodically observed at the tropical tropopause near 100 hPa, as well as the characteristic tape recorder signal up to about 10 hPa, providing evidence that the dehydration mechanism is well-captured. Our results confirm that the entry of tropospheric air into the tropical stratosphere is forced by large-scale wave dynamics, whereas radiative cooling regionally decelerates upwelling and can even cause downwelling. Thin cirrus forms in the cold air above cumulonimbus clouds, and the associated sedimentation of ice particles between 100 and 200 hPa reduces water mass fluxes by nearly two orders of magnitude compared to air mass fluxes. Transport into the stratosphere is supported by regional net radiative heating, to a large extent in the outer tropics. During summer very deep monsoon convection over Southeast Asia, centered over Tibet, moistens the stratosphere.

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

    Science.gov (United States)

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

    1985-01-01

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

  7. Influence of Aerosol Heating on the Stratospheric Transport of the Mt. Pinatubo Eruption

    Science.gov (United States)

    Aquila, Valentina; Oman, Luke D.; Stolarski, Richard S.

    2011-01-01

    On June 15th, 1991 the eruption of Mt. Pinatubo (15.1 deg. N, 120.3 Deg. E) in the Philippines injected about 20 Tg of sulfur dioxide in the stratosphere, which was transformed into sulfuric acid aerosol. The large perturbation of the background aerosol caused an increase in temperature in the lower stratosphere of 2-3 K. Even though stratospheric winds climatological]y tend to hinder the air mixing between the two hemispheres, observations have shown that a large part of the SO2 emitted by Mt. Pinatubo have been transported from the Northern to the Southern Hemisphere. We simulate the eruption of Mt. Pinatubo with the Goddard Earth Observing System (GEOS) version 5 global climate model, coupled to the aerosol module GOCART and the stratospheric chemistry module StratChem, to investigate the influence of the eruption of Mt. Pinatubo on the stratospheric transport pattern. We perform two ensembles of simulations: the first ensemble consists of runs without coupling between aerosol and radiation. In these simulations the plume of aerosols is treated as a passive tracer and the atmosphere is unperturbed. In the second ensemble of simulations aerosols and radiation are coupled. We show that the set of runs with interactive aerosol produces a larger cross-equatorial transport of the Pinatubo cloud. In our simulations the local heating perturbation caused by the sudden injection of volcanic aerosol changes the pattern of the stratospheric winds causing more intrusion of air from the Northern into the Southern Hemisphere. Furthermore, we perform simulations changing the injection height of the cloud, and study the transport of the plume resulting from the different scenarios. Comparisons of model results with SAGE II and AVHRR satellite observations will be shown.

  8. COS in the stratosphere. [sulfuric acid aerosol precursor

    Science.gov (United States)

    Inn, E. C. Y.; Vedder, J. F.; Tyson, B. J.; Ohara, D.

    1979-01-01

    Carbonyl sulfide (COS) has been detected in the stratosphere, and mixing ratio measurements are reported for altitudes of 15.2 to 31.2 km. A large volume, cryogenic sampling system mounted on board a U-2 aircraft has been used for lower stratosphere measurements and a balloon platform for measurement at 31.2 km. These observations and measurements strongly support the concept that stratospheric COS is an important precursor in the formation of sulfuric acid aerosols.

  9. Effects of El Chichon volcanic effluents on stratospheric aerosol dynamics

    Science.gov (United States)

    Pueschel, R. F.; Snetsinger, K. G.; Russell, P. B.; Oberbeck, V. R.; Livingston, J. M.

    1988-01-01

    The effects of El Chichon's April 1982 eruption on stratospheric aerosol dynamics are presently discussed in terms of log-normal size distributions over 15-20 km sample altitudes between 30 and 45 deg N over the contiguous U.S. After collection, samples were studied by SEM, and log-normal size distributions were fitted to the data-points obtained. It is found that stratospheric aerosol behavior is explainable by the laws of aerosol mechanics more easily than has been the case for tropospheric aerosol, for which the source-sink relationship is much more complex.

  10. Lidar Observations of Stratospheric Aerosol Layer After the Mt. Pinatubo Volcanic Eruption

    Science.gov (United States)

    Nagai, Tomohiro; Uchino, Osamu; Fujimoto, Toshifumi

    1992-01-01

    The volcano Mt. Pinatubo located on the Luzon Island, Philippines, had explosively erupted on June 15, 1991. The volcanic eruptions such as volcanic ash, SO2 and H2O reached into the stratosphere over 30 km altitude by the NOAA-11 satellite observation and this is considered one of the biggest volcanic eruptions in this century. A grandiose volcanic eruption influences the atmosphere seriously and causes many climatic effects globally. There had been many impacts on radiation, atmospheric temperature and stratospheric ozone after some past volcanic eruptions. The main cause of volcanic influence depends on stratospheric aerosol, that stay long enough to change climate and other meteorological conditions. Therefore it is very important to watch stratospheric aerosol layers carefully and continuously. Standing on this respect, we do not only continue stratospheric aerosol observation at Tsukuba but also have urgently developed another lidar observational point at Naha in Okinawa Island. This observational station could be thought valuable since there is no lidar observational station in this latitudinal zone and it is much nearer to Mt. Pinatubo. Especially, there is advantage to link up these two stations on studying the transportation mechanism in the stratosphere. In this paper, we present the results of lidar observations at Tsukuba and Naha by lidar systems with Nd:YAG laser.

  11. Solar geoengineering using solid aerosol in the stratosphere

    Science.gov (United States)

    Weisenstein, D. K.; Keith, D. W.; Dykema, J. A.

    2015-10-01

    Solid aerosol particles have long been proposed as an alternative to sulfate aerosols for solar geoengineering. Any solid aerosol introduced into the stratosphere would be subject to coagulation with itself, producing fractal aggregates, and with the natural sulfate aerosol, producing liquid-coated solids. Solid aerosols that are coated with sulfate and/or have formed aggregates may have very different scattering properties and chemical behavior than uncoated non-aggregated monomers do. We use a two-dimensional (2-D) chemistry-transport-aerosol model to capture the dynamics of interacting solid and liquid aerosols in the stratosphere. As an example, we apply the model to the possible use of alumina and diamond particles for solar geoengineering. For 240 nm radius alumina particles, for example, an injection rate of 4 Tg yr-1 produces a global-average shortwave radiative forcing of -1.2 W m-2 and minimal self-coagulation of alumina although almost all alumina outside the tropics is coated with sulfate. For the same radiative forcing, these solid aerosols can produce less ozone loss, less stratospheric heating, and less forward scattering than sulfate aerosols do. Our results suggest that appropriately sized alumina, diamond or similar high-index particles may have less severe technology-specific risks than sulfate aerosols do. These results, particularly the ozone response, are subject to large uncertainties due to the limited data on the rate constants of reactions on the dry surfaces.

  12. Lower stratospheric aerosols at a tropical latitude station

    Science.gov (United States)

    Krishnamurthy, B. V.; Parameswaran, K.; Rose, K. O.; Satyanarayana, M.

    1989-01-01

    A pulsed ruby lidar has been in regular operation at the tropical station Trivandrum (8 deg 33 sec N, 76 deg 57 sec E) since October 1986. The lidar data were analyzed to obtain monthly mean aerosol extinction at lower stratospheric altitudes. The monthly mean variation of aerosol extinction shows a peak in March to April with a trough in the winter months. This behavior is compared with that of temperature at the same altitude, obtained from balloonsonde measurements at the same station. It is found that there is a negative correlation between the two with high extinction values corresponding to low temperature values and vice versa. This is attributed to the stratospheric aerosol microphysical processes. The association of stratospheric aerosol extinction with the tropopause altitude and temperature was studied along with the implications of these results.

  13. Small volcanic eruptions and the stratospheric sulfate aerosol burden

    Science.gov (United States)

    Pyle, David M.

    2012-09-01

    Understanding of volcanic activity and its impacts on the atmosphere has evolved in discrete steps, associated with defining eruptions. The eruption of Krakatau, Indonesia, in August 1883 was the first whose global reach was recorded through observations of atmospheric phenomena around the world (Symons 1888). The rapid equatorial spread of Krakatau's ash cloud revealed new details of atmospheric circulation, while the vivid twilights and other optical phenomena were soon causally linked to the effects of particles and gases released from the volcano (e.g. Stothers 1996, Schroder 1999, Hamilton 2012). Later, eruptions of Agung, Bali (1963), El Chichón, Mexico (1982) and Pinatubo, Philippines (1991) led to a fuller understanding of how volcanic SO2 is transformed to a long-lived stratospheric sulfate aerosol, and its consequences (e.g. Meinel and Meinel 1967, Rampino and Self 1982, Hoffman and Rosen 1983, Bekki and Pyle 1994, McCormick et al 1995). While our ability to track the dispersal of volcanic emissions has been transformed since Pinatubo, with the launch of fleets of Earth-observing satellites (e.g. NASA's A-Train; ESA's MetOp) and burgeoning networks of ground-based remote-sensing instruments (e.g. lidar and sun-photometers; infrasound and lightning detection systems), there have been relatively few significant eruptions. Thus, there have been limited opportunities to test emerging hypotheses including, for example, the vexed question of the role of 'smaller' explosive eruptions in perturbations of the atmosphere—those that may just be large enough to reach the stratosphere (of size 'VEI 3', Newhall and Self 1982, Pyle 2000). Geological evidence, from ice-cores and historical eruptions, suggests that small explosive volcanic eruptions with the potential to transport material into the stratosphere should be frequent (5-10 per decade), and responsible for a significant proportion of the long-term time-averaged flux of volcanic sulfur into the stratosphere

  14. The global middle-atmosphere aerosol model MAECHAM5-SAM2: comparison with satellite and in-situ observations

    Directory of Open Access Journals (Sweden)

    R. Hommel

    2011-09-01

    Full Text Available In this paper we investigate results from a three-dimensional middle-atmosphere aerosol-climate model which has been developed to study the evolution of stratospheric aerosols. Here we focus on the stratospheric background period and evaluate several key quantities of the global distribution of stratospheric aerosols and their precursors with observations and other model studies. It is shown that the model fairly well reproduces in situ observations of the aerosol size and number concentrations in the upper troposphere and lower stratosphere (UT/LS. Compared to measurements from the limb-sounding SAGE II satellite instrument, modelled integrated aerosol quantities are more biased the lower the moment of the aerosol population is. Both findings are consistent with earlier work analysing the quality of SAGE II retrieved e.g. aerosol surface area densities in the volcanically unperturbed stratosphere (SPARC/ASAP, 2006; Thomason et al., 2008; Wurl et al., 2010.

    The model suggests that new particles are formed over large areas of the LS, albeit nucleation rates in the upper troposphere are at least one order of magnitude larger than those in the stratosphere. Hence, we suggest that both, tropospheric sulphate aerosols and particles formed in situ in the LS are maintaining the stability of the stratospheric aerosol layer in the absence of direct stratospheric emissions from volcanoes. Particle size distributions are clearly bimodal, except in the upper branches of the stratospheric aerosol layer where aerosols evaporate. Modelled concentrations of condensation nuclei (CN are smaller than measured in regions of the aerosol layer where aerosol mixing ratios are largest. This points to an overestimated particle growth by coagulation.

    Transport regimes of tropical stratospheric aerosol have been identified from modelled aerosol mixing ratios and correspond to those deduced from satellite extinction measurements. We found that convective

  15. The impact of geoengineering aerosols on stratospheric temperature and ozone

    Energy Technology Data Exchange (ETDEWEB)

    Heckendorn, P; Luo, B P; Rozanov, E; Schraner, M; Peter, T [Institute for Atmospheric and Climate Science, ETH Zurich, 8092 Zurich (Switzerland); Weisenstein, D [AER, Lexington, MA (United States); Fueglistaler, S [DAMTP, University of Cambridge (United Kingdom); Thomason, L W, E-mail: patricia.heckendorn@env.ethz.c [NASA Langley Research Center, Hampton, VA (United States)

    2009-10-15

    Anthropogenic greenhouse gas emissions are warming the global climate at an unprecedented rate. Significant emission reductions will be required soon to avoid a rapid temperature rise. As a potential interim measure to avoid extreme temperature increase, it has been suggested that Earth's albedo be increased by artificially enhancing stratospheric sulfate aerosols. We use a 3D chemistry climate model, fed by aerosol size distributions from a zonal mean aerosol model, to simulate continuous injection of 1-10 Mt/a into the lower tropical stratosphere. In contrast to the case for all previous work, the particles are predicted to grow to larger sizes than are observed after volcanic eruptions. The reason is the continuous supply of sulfuric acid and hence freshly formed small aerosol particles, which enhance the formation of large aerosol particles by coagulation and, to a lesser extent, by condensation. Owing to their large size, these particles have a reduced albedo. Furthermore, their sedimentation results in a non-linear relationship between stratospheric aerosol burden and annual injection, leading to a reduction of the targeted cooling. More importantly, the sedimenting particles heat the tropical cold point tropopause and, hence, the stratospheric entry mixing ratio of H{sub 2}O increases. Therefore, geoengineering by means of sulfate aerosols is predicted to accelerate the hydroxyl catalyzed ozone destruction cycles and cause a significant depletion of the ozone layer even though future halogen concentrations will be significantly reduced.

  16. The Impact of Geoengineering Aerosols on Stratospheric Temperature and Ozone

    Science.gov (United States)

    Heckendorn, P.; Weisenstein, D.; Fueglistaler, S.; Luo, B. P.; Rozanov, E.; Schraner, M.; Thomason, L. W.; Peter, T.

    2011-01-01

    Anthropogenic greenhouse gas emissions are warming the global climate at an unprecedented rate. Significant emission reductions will be required soon to avoid a rapid temperature rise. As a potential interim measure to avoid extreme temperature increase, it has been suggested that Earth's albedo be increased by artificially enhancing stratospheric sulfate aerosols. We use a 3D chemistry climate model, fed by aerosol size distributions from a zonal mean aerosol model. to simulate continuous injection of 1-10 Mt/a into the lower tropical stratosphere. In contrast to the case for all previous work, the particles are predicted to grow to larger sizes than are observed after volcanic eruptions. The reason is the continuous supply of sulfuric acid and hence freshly formed small aerosol particles, which enhance the formation of large aerosol particles by coagulation and, to a lesser extent, by condensation. Owing to their large size, these particles have a reduced albedo. Furthermore, their sedimentation results in a non-linear relationship between stratospheric aerosol burden and annual injection, leading to a reduction of the targeted cooling. More importantly, the sedimenting particles heat the tropical cold point tropopause and, hence, the stratospheric entry mixing ratio of H2O increases. Therefore, geoengineering by means of sulfate aerosols is predicted to accelerate the hydroxyl catalyzed ozone destruction cycles and cause a significant depletion of the ozone layer even though future halogen concentrations will he significantly reduced.

  17. The sensitivity to polarization in stratospheric aerosol retrievals from limb scattered sunlight measurements

    Science.gov (United States)

    Elash, B. J.; Bourassa, A. E.; Rieger, L. A.; Dueck, S. R.; Zawada, D. J.; Degenstein, D. A.

    2017-03-01

    Satellite measurements of limb scattered sunlight at visible and near infrared wavelengths have been used successfully for several years to retrieve the vertical profile of stratospheric aerosol extinction coefficient. The existing satellite measurements are of the total radiance, with very little knowledge or impact of the polarization state of the limb radiance. Recently proposed instrument concepts for stratospheric aerosol profiling have been designed to measure the linearly polarized radiance. Yet, to date, the impact of the polarized measurement on the retrievals has not been systematically studied. Here we use a fully spherical, multiple scattering radiative transfer model to perform a sensitivity study on the effects of the polarized measurement on stratospheric aerosol extinction retrievals through specific investigations of the aerosol signal fraction in polarized measurements, potential retrieval bias, and achievable precision. In this study,we simulate both total and linearly polarized measurements, for a wide range of limb viewing geometries that are encountered in typical low earth orbits and for various aerosol loading scenarios. The orientation of the linear polarization with respect to the horizon is also studied. Taking into account instrument signal to noise levels it is found that in general, the linear polarization can be used as effectively as the total radiance measurement, with consideration of instrument signal to noise capabilities; however the horizontal polarization is more promising in terms of signal magnitude.

  18. Solar geoengineering using solid aerosol in the stratosphere

    Directory of Open Access Journals (Sweden)

    D. K. Weisenstein

    2015-04-01

    Full Text Available Solid aerosol particles have long been proposed as an alternative to sulfate aerosols for solar geoengineering. Any solid aerosol introduced into the stratosphere would be subject to coagulation with itself, producing fractal aggregates, and with the natural sulfate aerosol, producing liquid-coated solids. Solid aerosols that are coated with sulfate and/or have formed aggregates may have very different scattering properties and chemical behavior than do uncoated non-aggregated monomers. We use a two-dimensional chemical transport model to capture the dynamics of interacting solid and liquid aerosols in the stratosphere. As an example, we apply the model to the possible use of alumina and diamond particles for solar geoengineering. For 240 nm radius alumina particles, for example, an injection rate of 4 Mt yr−1 produces a global-average radiative forcing of 1.3 W m−2 and minimal self-coagulation of alumina yet almost all alumina outside the tropics is coated with sulfate. For the same radiative forcing, these solid aerosols can produce less ozone loss, less stratospheric heating, and less forward scattering than do sulfate aerosols. Our results suggest that appropriately sized alumina, diamond or similar high-index particles may have less severe technology-specific risks than do sulfate aerosols. These results, particularly the ozone response, are subject to large uncertainties due the limited data on the rate constants of reactions on the dry surfaces.

  19. Impact of geoengineered aerosols on the troposphere and stratosphere

    Energy Technology Data Exchange (ETDEWEB)

    Tilmes, S.; Garcia, Rolando R.; Kinnison, Douglas E.; Gettelman, A.; Rasch, Philip J.

    2009-06-27

    A coupled chemistry climate model, the Whole Atmosphere Community Climate Model was used to perform a transient climate simulation to quantify the impact of geoengineered aerosols on atmospheric processes. In contrast to previous model studies, the impact on stratospheric chemistry, including heterogeneous chemistry in the polar regions, is considered in this simulation. In the geoengineering simulation, a constant stratospheric distribution of volcanic-sized, liquid sulfate aerosols is imposed in the period 2020–2050, corresponding to an injection of 2 Tg S/a. The aerosol cools the troposphere compared to a baseline simulation. Assuming an Intergovernmental Panel on Climate Change A1B emission scenario, global warming is delayed by about 40 years in the troposphere with respect to the baseline scenario. Large local changes of precipitation and temperatures may occur as a result of geoengineering. Comparison with simulations carried out with the Community Atmosphere Model indicates the importance of stratospheric processes for estimating the impact of stratospheric aerosols on the Earth’s climate. Changes in stratospheric dynamics and chemistry, especially faster heterogeneous reactions, reduce the recovery of the ozone layer in middle and high latitudes for the Southern Hemisphere. In the geoengineering case, the recovery of the Antarctic ozone hole is delayed by about 30 years on the basis of this model simulation. For the Northern Hemisphere, a onefold to twofold increase of the chemical ozone depletion occurs owing to a simulated stronger polar vortex and colder temperatures compared to the baseline simulation, in agreement with observational estimates.

  20. SAGE II Measurements of Stratospheric Aerosol Properties at Non-Volcanic Levels

    Science.gov (United States)

    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.

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

    Science.gov (United States)

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

    1993-01-01

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

  2. Trends in stratospheric ozone derived from merged SAGE II and Odin-OSIRIS satellite observations

    Directory of Open Access Journals (Sweden)

    A. E. Bourassa

    2014-03-01

    Full Text Available Stratospheric ozone profile measurements from the Stratospheric Aerosol and Gas Experiment (SAGE II satellite instrument (1984–2005 are combined with those from the Optical Spectrograph and InfraRed Imager System (OSIRIS instrument on the Odin satellite (2001–Present to quantify interannual variability and decadal trends in stratospheric ozone between 60° S and 60° N. These data are merged into a multi-instrument, long-term stratospheric ozone record (1984–present by analyzing the measurements during the overlap period of 2002–2005 when both satellite instruments were operational. The variability in the deseasonalized time series is fit using multiple linear regression with predictor basis functions including the quasi-biennial oscillation, El Niño-Southern Oscillation index, solar activity proxy, and the pressure at the tropical tropopause, in addition to two linear trends (one before and one after 1997, from which the decadal trends in ozone are derived. From 1984–1997, there are statistically significant negative trends of 5–10% per decade throughout the stratosphere between approximately 30–50 km. From 1997–present, a statistically significant recovery of 3–8% per decade has taken place throughout most of the stratosphere with the notable exception between 40° S–40° N below approximately 22 km where the negative trend continues. The recovery is not significant between 25–35 km altitude when accounting for a conservative estimate of instrument drift.

  3. Reduction of photosynthetically active radiation under extreme stratospheric aerosol loads

    Energy Technology Data Exchange (ETDEWEB)

    Gerstl, S.A.W.; Zardecki, A.

    1981-08-01

    The recently published hypothesis that the Cretaceous-Tertiary extinctions might be caused by an obstruction of sunlight is tested by model calculations. First we compute the total mass of stratospheric aerosols under normal atmospheric conditions for four different (measured) aerosol size distributions and vertical profiles. For comparison, the stratospheric dust masses after four volcanic eruptions are also evaluated. Detailed solar radiative transfer calculations are then performed for artificially increased aerosol amounts until the postulated darkness scenario is obtained. Thus we find that a total stratospheric aerosol mass between 1 and 4 times 10/sup 1/ g is sufficient to reduce photosynthesis to 10/sup -3/ of normal. We also infer from this result tha the impact of a 0.4- to 3-km-diameter asteroid or a close encounter with a Halley-size comet may deposit that amount of particulates into the stratosphere. The darkness scenario of Alvarez et al. is thus shown to be a possible extinction mechanism, even with smaller size asteroids of comets than previously estimated.

  4. Possible effect of extreme solar energetic particle event of 20 January 2005 on polar stratospheric aerosols: direct observational evidence

    Directory of Open Access Journals (Sweden)

    I. A. Mironova

    2012-01-01

    Full Text Available Energetic cosmic rays are the main source of ionization of the low-middle atmosphere, leading to associated changes in atmospheric properties. Via the hypothetical influence of ionization on aerosol growth and facilitated formation of clouds, this may be an important indirect link relating solar variability to climate. This effect is highly debated, however, since the proposed theoretical mechanisms still remain illusive and qualitative, and observational evidence is inconclusive and controversial. Therefore, important questions regarding the existence and magnitude of the effect, and particularly the fraction of aerosol particles that can form and grow, are still open. Here we present empirical evidence of the possible effect caused by cosmic rays upon polar stratospheric aerosols, based on a case study of an extreme solar energetic particle (SEP event of 20 January 2005. Using aerosol data obtained over polar regions from different satellites with optical instruments that were operating during January 2005, such as the Stratospheric Aerosol and Gas Experiment III (SAGE III, and Optical Spectrograph and Infrared Imaging System (OSIRIS, we found a significant simultaneous change in aerosol properties in both the Southern and Northern Polar regions in temporal association with the SEP event. We speculate that ionization of the atmosphere, which was abnormally high in the lower stratosphere during the extreme SEP event, might have led to formation of new particles and/or growth of preexisting ultrafine particles in the polar stratospheric region. However, a detailed interpretation of the effect is left for subsequent studies. This is the first time high vertical resolution measurements have been used to discuss possible production of stratospheric aerosols under the influence of cosmic ray induced ionization. The observed effect is marginally detectable for the analyzed severe SEP event and can be undetectable for the majority of weak

  5. An overview of geoengineering of climate using stratospheric sulphate aerosols

    Energy Technology Data Exchange (ETDEWEB)

    Rasch, Philip J.; Tilmes, S.; Turco, Richard P.; Robock, Alan; Oman, Luke; Chen, Chih-Chieh; Stenchikov, Georgiy; Garcia, Rolando R.

    2010-01-01

    We provide an overview of geoengineering by stratospheric sulphate aerosols. The state of understanding about this topic as of early 2008 is reviewed, summarizing the past 30 years of work in the area, highlighting some very recent studies using climate models, and discussing methods used to deliver sulphur species to the stratosphere. The studies reviewed here suggest that sulphate aerosols can counteract the globally averaged temperature increase associated with increasing greenhouse gases, and reduce changes to some other components of the Earth system. There are likely to be remaining regional climate changes after geoengineering, with some regions experiencing significant changes in temperature or precipitation. The aerosols also serve as surfaces for heterogeneous chemistry resulting in increased ozone depletion. The delivery of sulphur species to the stratosphere in a way that will produce particles of the right size is shown to be a complex and potentially very difficult task. Two simple delivery scenarios are explored, but similar exercises will be needed for other suggested delivery mechanisms. While the introduction of the geoengineering source of sulphate aerosol will perturb the sulphur cycle of the stratosphere signicantly, it is a small perturbation to the total (stratosphere and troposphere) sulphur cycle. The geoengineering source would thus be a small contributor to the total global source of ‘acid rain’ that could be compensated for through improved pollution control of anthropogenic tropospheric sources. Some areas of research remain unexplored. Although ozone may be depleted, with a consequent increase to solar ultraviolet-B (UVB) energy reaching the surface and a potential impact on health and biological populations, the aerosols will also scatter and attenuate this part of the energy spectrum, and this may compensate the UVB enhancement associated with ozone depletion. The aerosol will also change the ratio of diffuse to direct energy

  6. An overview of geoengineering of climate using stratospheric sulphate aerosols.

    Science.gov (United States)

    Rasch, Philip J; Tilmes, Simone; Turco, Richard P; Robock, Alan; Oman, Luke; Chen, Chih-Chieh; Stenchikov, Georgiy L; Garcia, Rolando R

    2008-11-13

    We provide an overview of geoengineering by stratospheric sulphate aerosols. The state of understanding about this topic as of early 2008 is reviewed, summarizing the past 30 years of work in the area, highlighting some very recent studies using climate models, and discussing methods used to deliver sulphur species to the stratosphere. The studies reviewed here suggest that sulphate aerosols can counteract the globally averaged temperature increase associated with increasing greenhouse gases, and reduce changes to some other components of the Earth system. There are likely to be remaining regional climate changes after geoengineering, with some regions experiencing significant changes in temperature or precipitation. The aerosols also serve as surfaces for heterogeneous chemistry resulting in increased ozone depletion. The delivery of sulphur species to the stratosphere in a way that will produce particles of the right size is shown to be a complex and potentially very difficult task. Two simple delivery scenarios are explored, but similar exercises will be needed for other suggested delivery mechanisms. While the introduction of the geoengineering source of sulphate aerosol will perturb the sulphur cycle of the stratosphere signicantly, it is a small perturbation to the total (stratosphere and troposphere) sulphur cycle. The geoengineering source would thus be a small contributor to the total global source of 'acid rain' that could be compensated for through improved pollution control of anthropogenic tropospheric sources. Some areas of research remain unexplored. Although ozone may be depleted, with a consequent increase to solar ultraviolet-B (UVB) energy reaching the surface and a potential impact on health and biological populations, the aerosols will also scatter and attenuate this part of the energy spectrum, and this may compensate the UVB enhancement associated with ozone depletion. The aerosol will also change the ratio of diffuse to direct energy

  7. Stratospheric aerosols from the Sarychev volcano eruption in the 2009 Arctic summer

    Science.gov (United States)

    Jégou, F.; Berthet, G.; Brogniez, C.; Renard, J.-B.; François, P.; Haywood, J. M.; Jones, A.; Bourgeois, Q.; Lurton, T.; Auriol, F.; Godin-Beekmann, S.; Guimbaud, C.; Krysztofiak, G.; Gaubicher, B.; Chartier, M.; Clarisse, L.; Clerbaux, C.; Balois, J. Y.; Verwaerde, C.; Daugeron, D.

    2013-07-01

    Aerosols from the Sarychev volcano eruption (Kuril Islands, northeast of Japan) were observed in the Arctic lower stratosphere a few days after the strongest SO2 injection which occurred on 15 and 16 June 2009. From the observations provided by the Infrared Atmospheric Sounding Interferometer (IASI) an estimated 0.9 Tg of sulphur dioxide was injected into the upper troposphere and lower stratosphere (UTLS). The resultant stratospheric sulphate aerosols were detected from satellites by the Optical Spectrograph and Infrared Imaging System (OSIRIS) limb sounder and by the Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP) and from the surface by the Network for the Detection of Atmospheric Composition Changes (NDACC) lidar deployed at OHP (Observatoire de Haute-Provence, France). By the first week of July the aerosol plume had spread out over the entire Arctic region. The Sarychev-induced stratospheric aerosol over the Kiruna region (north of Sweden) was measured by the Stratospheric and Tropospheric Aerosol Counter (STAC) during eight balloon flights planned in August and September 2009. During this balloon campaign the Micro Radiomètre Ballon (MicroRADIBAL) and the Spectroscopie d'Absorption Lunaire pour l'Observation des Minoritaires Ozone et NOx (SALOMON) remote-sensing instruments also observed these aerosols. Aerosol concentrations returned to near-background levels by spring 2010. The effective radius, the surface area density (SAD), the aerosol extinction, and the total sulphur mass from STAC in situ measurements are enhanced with mean values in the range 0.15-0.21 μm, 5.5-14.7 μm2 cm-3, 5.5-29.5 × 10-4 km-1, and 4.9-12.6 × 10-10 kg[S] kg-1[air], respectively, between 14 km and 18 km. The observed and modelled e-folding time of sulphate aerosols from the Sarychev eruption is around 70-80 days, a value much shorter than the 12-14 months calculated for aerosols from the 1991 eruption of Mt Pinatubo. The OSIRIS stratospheric aerosol optical depth (AOD

  8. Stratospheric aerosols from the Sarychev volcano eruption in the 2009 Arctic summer

    Directory of Open Access Journals (Sweden)

    F. Jégou

    2013-02-01

    Full Text Available Aerosols from the Sarychev volcano eruption (Kuril Islands, northeast of Japan were observed in the Arctic lower stratosphere a few days after the strongest SO2 injection which occurred on 15 and 16 June 2009. From the observations provided by the Infrared Atmospheric Sounding Interferometer (IASI an estimated 0.9 Tg of sulphur dioxide was injected into the Upper Troposphere and Lower Stratosphere (UTLS. The resultant stratospheric sulphate aerosols were detected by the Optical Spectrograph and Infrared Imaging System (OSIRIS limb sounder and by the Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP satellite instruments. By the first week of July the aerosol plume had spread out over the entire Arctic region. The Sarychev-induced stratospheric aerosol over the Kiruna region (north of Sweden was measured by the Stratospheric and Tropospheric Aerosol Counter (STAC during eight balloon flights planned in August and September 2009. During this balloon campaign the Micro RADIomètre BALlon (MicroRADIBAL and the Spectroscopie d'Absorption Lunaire pour l'Observation des Minoritaires Ozone et NOx (SALOMON remote-sensing instruments also observed these aerosols. Aerosol concentrations returned to near-background levels by spring 2010. The effective radius, the Surface Area Density (SAD, the aerosol extinction, and the total sulphur mass from STAC in situ measurements are enhanced with mean values in the range 0.15–0.21 μm, 5.5–14.7 μm2 cm−3, 5.5–29.5×10−4 km−1, and 4.9–12.6×10−10 kg [S] kg−1 [air], respectively, between 14 km and 18 km. The observed and modelled e-folding time of sulphate aerosols from the Sarychev eruption is around 70–80 days, a value much shorter than the 12–14 months calculated for aerosols from the 1991 eruption of Mt. Pinatubo. The OSIRIS stratospheric Aerosol Optical Depth (AOD at 750 nm is enhanced by a factor of 6 with a

  9. Stratospheric aerosol particle size information in Odin-OSIRIS limb scatter spectra

    Directory of Open Access Journals (Sweden)

    L. A. Rieger

    2013-06-01

    Full Text Available The Optical Spectrograph and InfraRed Imaging System (OSIRIS on-board the Odin satellite has now taken over a decade of limb scatter measurements that have been used to retrieve the Version 5 stratospheric aerosol extinction product. This product is retrieved using a representative particle size distribution to calculate scattering cross sections and scattering phase functions for the forward model calculations. In this work the information content of OSIRIS measurements with respect to stratospheric aerosol is systematically examined for the purpose of retrieving particle size information along with the extinction coefficient. The benefit of using measurements at different wavelengths and scattering angles in the retrieval is studied and it is found that incorporation of the 1530 nm radiance measurement is key for a robust retrieval of particle size information. It is also found that using OSIRIS measurements at different solar geometries simultaneously provides little additional benefit. Based on these results, an improved aerosol retrieval algorithm is developed that couples the retrieval of aerosol extinction and mode radius of a log-normal particle size distribution. Comparison of these results with coincident measurements from SAGE III show agreement in retrieved extinction to within approximately 10% over the bulk of the aerosol layer, which is comparable to Version 5. The retrieved particle size, when converted to Ångström coefficient, shows good qualitative agreement with SAGE II measurements made at somewhat shorter wavelengths.

  10. Stratospheric aerosols from the Sarychev volcano eruption in the 2009 Arctic summer

    Directory of Open Access Journals (Sweden)

    F. Jégou

    2013-07-01

    Full Text Available Aerosols from the Sarychev volcano eruption (Kuril Islands, northeast of Japan were observed in the Arctic lower stratosphere a few days after the strongest SO2 injection which occurred on 15 and 16 June 2009. From the observations provided by the Infrared Atmospheric Sounding Interferometer (IASI an estimated 0.9 Tg of sulphur dioxide was injected into the upper troposphere and lower stratosphere (UTLS. The resultant stratospheric sulphate aerosols were detected from satellites by the Optical Spectrograph and Infrared Imaging System (OSIRIS limb sounder and by the Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP and from the surface by the Network for the Detection of Atmospheric Composition Changes (NDACC lidar deployed at OHP (Observatoire de Haute-Provence, France. By the first week of July the aerosol plume had spread out over the entire Arctic region. The Sarychev-induced stratospheric aerosol over the Kiruna region (north of Sweden was measured by the Stratospheric and Tropospheric Aerosol Counter (STAC during eight balloon flights planned in August and September 2009. During this balloon campaign the Micro Radiomètre Ballon (MicroRADIBAL and the Spectroscopie d'Absorption Lunaire pour l'Observation des Minoritaires Ozone et NOx (SALOMON remote-sensing instruments also observed these aerosols. Aerosol concentrations returned to near-background levels by spring 2010. The effective radius, the surface area density (SAD, the aerosol extinction, and the total sulphur mass from STAC in situ measurements are enhanced with mean values in the range 0.15–0.21 μm, 5.5–14.7 μm2 cm−3, 5.5–29.5 × 10−4 km−1, and 4.9–12.6 × 10−10 kg[S] kg−1[air], respectively, between 14 km and 18 km. The observed and modelled e-folding time of sulphate aerosols from the Sarychev eruption is around 70–80 days, a value much shorter than the 12–14 months calculated for aerosols from the 1991 eruption of Mt Pinatubo. The OSIRIS

  11. A Model Simulation of Pinatubo Volcanic Aerosols in the Stratosphere

    Science.gov (United States)

    Zhao , Jing-xia; Turco, Richard P.; Toon, Owen B.

    1995-01-01

    A one-dimensional, time-dependent model is used to study the chemical, microphysical, and radiative properties of volcanic aerosols produced by the Mount Pinatubo eruption on June 15, 1991. Our model treats gas-phase sulfur photochemistry, gas-to-particle conversion of sulfur, and the microphysics of sulfate aerosols and ash particles under stratospheric conditions. The dilution and diffusion of the volcanic eruption clouds are also accounted for in these conditions. Heteromolecular homogeneous and heterogeneous binary H2SO4/H2O nucleation, acid and water condensational growth, coagulation, and gravitational sedimentation are treated in detail in the model. Simulations suggested that after several weeks, the volcanic cloud was composed mainly of sulfuric acid/water droplets produced in situ from the SO2 emissions. The large amounts of SO2 (around 20 Mt) injected into the stratosphere by the Pinatubo eruption initiated homogeneous nucleation which generated a high concentration of small H2SO4/H2O droplets. These newly formed particles grew rapidly by condensation and coagulation in the first few months and then reach their stabilized sizes with effective radii in a range between 0.3 and 0.5 micron approximately one-half year after the eruption. The predicted volcanic cloud parameters reasonably agree with measurements in term of the vertical distribution and lifetime of the volcanic aerosols, their basic microphysical structures (e.g., size distribution, concentration, mass ratio, and surface area) and radiative properties. The persistent volcanic aerosols can produce significant anomalies in the radiation field, which have important climatic consequences. The large enhancement in aerosol surface area can result in measurable global stratospheric ozone depletion.

  12. A miniature particle counter LOAC under meteorological balloon for the survey of stratospheric aerosols - comparison with other datasets

    Science.gov (United States)

    Vignelles, Damien; Berthet, Bwenael; Renard, Jean-Baptiste; Rieger, Landon; Bourassa, Adam; Vernier, Jean-Paul; Taha, Ghassan; Khaykin, Sergey; Lurton, Thibaut; Jegou, Fabrice; Couté, Benoît; Duverger, Vincent

    2017-04-01

    Stratospheric aerosols contribute to the terrestrial radiative budget during large eruptive events but also during volcanic quiescent periods (Kremser et al. 2016). The survey of background stratospheric aerosols, especially in the middle stratosphere, is challenging due to extreme experimental conditions and low particle concentration. Furthermore, during periods of low volcanic activity, origins and optical properties of aerosols in the middle and high stratosphere are not well defined yet (Neely et al. 2011). We propose to study the capabilities of a new miniature particle counter called LOAC (Light Optical Aerosol Counter), light enough to be carried under meteorological balloons, whichensure a very good frequency of flights and designed to be able to measure and discriminate between several main aerosol types. The LOAC miniature particle counter has been initially designed for balloon-borne tropospheric studies (Renard et al. 2016).Metrological performances of the LOAC instrument have been determined in the laboratory and during balloon flights. Principal limitations of the use of LOAC in the stratosphere areinduced by the temperature variations and the influence of cosmic rays. A detection threshold has been determined in the laboratory to be of 0.8 particule.cm-3 in terms of concentration which also limits the use of LOAC in the stratosphere where aerosol concentrations during volcanic quiescent periods may be lower than this limit. Since June 2013, more than 100 hundred LOAC instruments have been launched under meteorological balloons during the ChArMEx and Voltaire-LOAC field campaigns. This dataset has been studied and compared to satellite records such as OSIRIS, OMPS, and CALIOPbut also to ground-based lidar data (NDACC lidar OHP) and outputs from the WACCM/CARMA model. Results show that large variations in stratospheric aerosols are well defined by satellite but less visible in LOAC records. Instrumental LOAC limitations in the stratosphere can explain

  13. Sulfuric acid deposition from stratospheric geoengineering with sulfate aerosols

    KAUST Repository

    Kravitz, Ben

    2009-07-28

    We used a general circulation model of Earth\\'s climate to conduct geoengineering experiments involving stratospheric injection of sulfur dioxide and analyzed the resulting deposition of sulfate. When sulfur dioxide is injected into the tropical or Arctic stratosphere, the main additional surface deposition of sulfate occurs in midlatitude bands, because of strong cross-tropopause flux in the jet stream regions. We used critical load studies to determine the effects of this increase in sulfate deposition on terrestrial ecosystems by assuming the upper limit of hydration of all sulfate aerosols into sulfuric acid. For annual injection of 5 Tg of SO2 into the tropical stratosphere or 3 Tg of SO2 into the Arctic stratosphere, neither the maximum point value of sulfate deposition of approximately 1.5 mEq m−2 a−1 nor the largest additional deposition that would result from geoengineering of approximately 0.05 mEq m−2 a−1 is enough to negatively impact most ecosystems.

  14. The role of carbonyl sulphide as a source of stratospheric sulphate aerosol and its impact on climate

    Directory of Open Access Journals (Sweden)

    C. Brühl

    2012-02-01

    Full Text Available Globally, carbonyl sulphide (COS is the most abundant sulphur gas in the atmosphere. Our chemistry-climate model (CCM of the lower and middle atmosphere with aerosol module realistically simulates the background stratospheric sulphur cycle, as observed by satellites in volcanically quiescent periods. The model results indicate that upward transport of COS from the troposphere largely controls the sulphur budget and the aerosol loading of the background stratosphere. This differs from most previous studies which indicated that short-lived sulphur gases are also important. The model realistically simulates the modulation of the particulate and gaseous sulphur abundance in the stratosphere by the quasi-biennial oscillation (QBO. In the lowermost stratosphere organic carbon aerosol contributes significantly to extinction. Further, using a chemical radiative convective model and recent spectra, we compute that the direct radiative forcing efficiency by 1 kg of COS is 724 times that of 1 kg CO2. Considering an anthropogenic fraction of 30% (derived from ice core data, this translates into an overall direct radiative forcing by COS of 0.003 W m−2. The direct global warming potentials of COS over time horizons of 20 and 100 yr are GWP(20 yr = 97 and GWP(100 yr = 27, respectively (by mass. Furthermore, stratospheric aerosol particles produced by the photolysis of COS (chemical feedback contribute to a negative direct solar radiative forcing, which in the CCM amounts to −0.007 W m−2 at the top of the atmosphere for the anthropogenic fraction, more than two times the direct warming forcing of COS. Considering that the lifetime of COS is twice that of stratospheric aerosols the warming and cooling tendencies approximately cancel.

  15. A lidar equipped with photon counter for measuring stratospheric aerosols

    Science.gov (United States)

    Zhou, Jun; Hu, Huanling

    1991-01-01

    A large lidar system was developed at the Anhui Institute of Optics and Fine Mechanics. It is composed of a high power frequency doubled Nd:YAG laser (120 mJ at 532 nm, 1 mrad), a 651 mm diameter receiving telescope, and a 64 channel photon counter. The lidar observations are controlled by an IBM PC/AT computer. One of the projects is to use the lidar system to make regular observations of stratospheric aerosols. Profiles of scattering ratio have been obtained since November 1989. Meanwhile, an Xe-Cl laser (308 nm wavelength) was assembled to allow the lidar to make measurements of vertical ozone distributions.

  16. Enhancement of stratospheric aerosols after solar proton event

    Directory of Open Access Journals (Sweden)

    O. I. Shumilov

    Full Text Available The lidar measurements at Verhnetulomski observatory (68.6°N, 31.8°E at Kola peninsula detected a considerable increase of stratospheric aerosol concentration after the solar proton event of GLE (ground level event type on the 16/02/84. This increase was located at precisely the same altitude range where the energetic solar protons lost their energy in the atmosphere. The aerosol layer formed precipitated quickly (1–2 km per day during 18, 19, and 20 February 1984, and the increase of R(H (backscattering ratio at 17 km altitude reached 40% on 20/02/84. We present the model calculation of CN (condensation nuclei altitude distribution on the basis of an ion-nucleation mechanism, taking into account the experimental energy distribution of incident solar protons. The meteorological situation during the event was also investigated.

  17. The Sectional Stratospheric Sulfate Aerosol module (S3A-v1) within the LMDZ general circulation model: description and evaluation against stratospheric aerosol observations

    Science.gov (United States)

    Kleinschmitt, Christoph; Boucher, Olivier; Bekki, Slimane; Lott, François; Platt, Ulrich

    2017-09-01

    Stratospheric aerosols play an important role in the climate system by affecting the Earth's radiative budget as well as atmospheric chemistry, and the capabilities to simulate them interactively within global models are continuously improving. It is important to represent accurately both aerosol microphysical and atmospheric dynamical processes because together they affect the size distribution and the residence time of the aerosol particles in the stratosphere. The newly developed LMDZ-S3A model presented in this article uses a sectional approach for sulfate particles in the stratosphere and includes the relevant microphysical processes. It allows full interaction between aerosol radiative effects (e.g. radiative heating) and atmospheric dynamics, including e.g. an internally generated quasi-biennial oscillation (QBO) in the stratosphere. Sulfur chemistry is semi-prescribed via climatological lifetimes. LMDZ-S3A reasonably reproduces aerosol observations in periods of low (background) and high (volcanic) stratospheric sulfate loading, but tends to overestimate the number of small particles and to underestimate the number of large particles. Thus, it may serve as a tool to study the climate impacts of volcanic eruptions, as well as the deliberate anthropogenic injection of aerosols into the stratosphere, which has been proposed as a method of geoengineering to abate global warming.

  18. Observations of Ozone-aerosol Correlated Behaviour in the Lower Stratosphere During the EASOE Campaign

    Science.gov (United States)

    Digirolamo, P.; Cacciani, M.; Disarra, A.; Fiocco, G.; Fua, D.; Joergensen, T. S.; Knudsen, B.; Larsen, N.

    1992-01-01

    The question of possible interactions between ozone and stratospheric aerosol has been open for a long time. Measurements carried out after the Mt. Agung and El Chicon eruptions showed evidence of negative correlations between the presence of volcanic stratospheric aerosols and ozone concentration. Evidence for negative correlations in the polar winter has been also found. It is only after the discovery of the Antarctic ozone hole that catalytic effects related to low temperature heterogeneous chemistry have become the object of much investigation, now extended to the role of volcanic aerosol in the ozone reduction. These phenomena can be the object of various interpretations, not mutually exclusive, including the effect of transport, diffuse radiation as well as heterogeneous chemistry. The present paper provides preliminary results of simultaneous measurements of ozone and aerosol, carried out at Thule, Greenland, during the winter 1991-92. The European Stratospheric Ozone Experiment (EASOE) was aimed at monitoring the winter Arctic stratosphere in order to obtain a deeper insight of the ozone destruction processes taking place in the polar regions. A large amount of aerosol was injected into the lower stratosphere by the recent eruption of Volcano Pinatubo. A lidar system, already operational in Thule since November 1990, has provided detailed measurements of the stratospheric aerosol concentration during EASOE. In the same period, a large number of ozonesondes were launched. Although no PSC formation was detected over Thule, the simultaneous measurement of the stratospheric aerosol and ozone profiles give the possibility to study interactions occurring in the stratosphere between these two constituents.

  19. Orbit control of a stratospheric satellite with parameter uncertainties

    Science.gov (United States)

    Xu, Ming; Huo, Wei

    2016-12-01

    When a stratospheric satellite travels by prevailing winds in the stratosphere, its cross-track displacement needs to be controlled to keep a constant latitude orbital flight. To design the orbit control system, a 6 degree-of-freedom (DOF) model of the satellite is established based on the second Lagrangian formulation, it is proven that the input/output feedback linearization theory cannot be directly implemented for the orbit control with this model, thus three subsystem models are deduced from the 6-DOF model to develop a sequential nonlinear control strategy. The control strategy includes an adaptive controller for the balloon-tether subsystem with uncertain balloon parameters, a PD controller based on feedback linearization for the tether-sail subsystem, and a sliding mode controller for the sail-rudder subsystem with uncertain sail parameters. Simulation studies demonstrate that the proposed control strategy is robust to uncertainties and satisfies high precision requirements for the orbit flight of the satellite.

  20. Stratospheric background aerosol and polar cloud observations by laser backscattersonde within the framework of the European project "Stratospheric Regular Sounding"

    Directory of Open Access Journals (Sweden)

    A. Adriani

    Full Text Available The Stratospheric Regular Sounding project was planned to measure regularly the vertical profiles of several tracers like ozone, water vapor, NOx, ClOx and BrOx radicals, aerosol, pressure and temperature, at three latitudes, to discriminate between the transport and photochemical terms which control their distribution. As part of this project, the "Istituto di Fisica dell'Atmosfera" launched nine laser backscattersondes (LABS on board stratospheric balloons to make observations of background aerosol and PSCs. LABS was launched with an optical particle counter operated by the University of Wyoming. Observations have been performed in the arctic, mid-latitudes and tropical regions in different seasons. Polar stratospheric clouds have been observed in areas inside and outside the polar vortex edge. A background aerosol was observed both in mid-latitudes and in arctic regions with a backscattering ratio of 1.2 at 692 nm. Very stratified aerosol layers, possibly transported into the lower stratosphere by deep convective systems, have been observed in the lower stratosphere between 20 and 29 km in the tropics in the Southern Hemisphere.

    Key words. Atmospheric composition and structure (aerosols and particles; middle atmosphere – composition and chemistry; instruments and techniques

  1. Global two-channel AVHRR aerosol climatology: effects of stratospheric aerosols and preliminary comparisons with MODIS and MISR retrievals

    Energy Technology Data Exchange (ETDEWEB)

    Geogdzhayev, Igor V. [Department of Applied Physics and Applied Mathematics, Columbia University, 2880 Broadway, New York, NY 10025 (United States); NASA Goddard Institute for Space Studies, 2880 Broadway, New York, NY 10025 (United States); Mishchenko, Michael I. [NASA Goddard Institute for Space Studies, 2880 Broadway, New York, NY 10025 (United States)]. E-mail: crmim@giss.nasa.gov; Liu Li [NASA Goddard Institute for Space Studies, 2880 Broadway, New York, NY 10025 (United States); Department of Earth and Environmental Sciences, Columbia University, 2880 Broadway, New York, NY 10025 (United States); Remer, Lorraine [NASA Goddard Space Flight Center, Code 913, Greenbelt, MD 20771 (United States)

    2004-10-15

    We present an update on the status of the global climatology of the aerosol column optical thickness and Angstrom exponent derived from channel-1 and -2 radiances of the Advanced Very High Resolution Radiometer (AVHRR) in the framework of the Global Aerosol Climatology Project (GACP). The latest version of the climatology covers the period from July 1983 to September 2001 and is based on an adjusted value of the diffuse component of the ocean reflectance as derived from extensive comparisons with ship sun-photometer data. We use the updated GACP climatology and Stratospheric Aerosol and Gas Experiment (SAGE) data to analyze how stratospheric aerosols from major volcanic eruptions can affect the GACP aerosol product. One possible retrieval strategy based on the AVHRR channel-1 and -2 data alone is to infer both the stratospheric and the tropospheric aerosol optical thickness while assuming fixed microphysical models for both aerosol components. The second approach is to use the SAGE stratospheric aerosol data in order to constrain the AVHRR retrieval algorithm. We demonstrate that the second approach yields a consistent long-term record of the tropospheric aerosol optical thickness and Angstrom exponent. Preliminary comparisons of the GACP aerosol product with MODerate resolution Imaging Spectrometer (MODIS) and Multiangle Imaging Spectro-Radiometer aerosol retrievals show reasonable agreement, the GACP global monthly optical thickness being lower than the MODIS one by approximately 0.03. Larger differences are observed on a regional scale. Comparisons of the GACP and MODIS Angstrom exponent records are less conclusive and require further analysis.

  2. New satellite project Aerosol-UA: Remote sensing of aerosols in the terrestrial atmosphere

    Science.gov (United States)

    Milinevsky, G.; Yatskiv, Ya.; Degtyaryov, O.; Syniavskyi, I.; Mishchenko, M.; Rosenbush, V.; Ivanov, Yu.; Makarov, A.; Bovchaliuk, A.; Danylevsky, V.; Sosonkin, M.; Moskalov, S.; Bovchaliuk, V.; Lukenyuk, A.; Shymkiv, A.; Udodov, E.

    2016-06-01

    We discuss the development of the Ukrainian space project Aerosol-UA which has the following three main objectives: (1) to monitor the spatial distribution of key characteristics of terrestrial tropospheric and stratospheric aerosols; (2) to provide a comprehensive observational database enabling accurate quantitative estimates of the aerosol contribution to the energy budget of the climate system; and (3) quantify the contribution of anthropogenic aerosols to climate and ecological processes. The remote sensing concept of the project is based on precise orbital measurements of the intensity and polarization of sunlight scattered by the atmosphere and the surface with a scanning polarimeter accompanied by a wide-angle multispectral imager-polarimeter. Preparations have already been made for the development of the instrument suite for the Aerosol-UA project, in particular, of the multi-channel scanning polarimeter (ScanPol) designed for remote sensing studies of the global distribution of aerosol and cloud properties (such as particle size, morphology, and composition) in the terrestrial atmosphere by polarimetric and spectrophotometric measurements of the scattered sunlight in a wide range of wavelengths and viewing directions from which a scene location is observed. ScanPol is accompanied by multispectral wide-angle imager-polarimeter (MSIP) that serves to collect information on cloud conditions and Earth's surface image. Various components of the polarimeter ScanPol have been prototyped, including the opto-mechanical and electronic assemblies and the scanning mirror controller. Preliminary synthetic data simulations for the retrieval of aerosol parameters over land surfaces have been performed using the Generalized Retrieval of Aerosol and Surface Properties (GRASP) algorithm. Methods for the validation of satellite data using ground-based observations of aerosol properties are also discussed. We assume that designing, building, and launching into orbit a multi

  3. New Satellite Project Aerosol-UA: Remote Sensing of Aerosols in the Terrestrial Atmosphere

    Science.gov (United States)

    Milinevsky, G.; Yatskiv, Ya.; Degtyaryov, O.; Syniavskyi, I.; Mishchenko, Michael I.; Rosenbush, V.; Ivanov, Yu.; Makarov, A.; Bovchaliuk, A.; Danylevsky, V.; Sosonkin, M.; Moskalov, S.; Bovchaliuk, V; Lukenyuk, A.; Shymkiv, A.

    2016-01-01

    We discuss the development of the Ukrainian space project Aerosol-UA which has the following three main objectives: (1) to monitor the spatial distribution of key characteristics of terrestrial tropospheric and stratospheric aerosols; (2) to provide a comprehensive observational database enabling accurate quantitative estimates of the aerosol contribution to the energy budget of the climate system; and (3) quantify the contribution of anthropogenic aerosols to climate and ecological processes. The remote sensing concept of the project is based on precise orbital measurements of the intensity and polarization of sunlight scattered by the atmosphere and the surface with a scanning polarimeter accompanied by a wide-angle multispectral imager-polarimeter. Preparations have already been made for the development of the instrument suite for the Aerosol-UA project, in particular, of the multi-channel scanning polarimeter (ScanPol) designed for remote sensing studies of the global distribution of aerosol and cloud properties (such as particle size, morphology, and composition) in the terrestrial atmosphere by polarimetric and spectrophotometric measurements of the scattered sunlight in a wide range of wavelengths and viewing directions from which a scene location is observed. ScanPol is accompanied by multispectral wide-angle imager-polarimeter (MSIP) that serves to collect information on cloud conditions and Earths surface image. Various components of the polarimeter ScanPol have been prototyped, including the opto-mechanical and electronic assemblies and the scanning mirror controller. Preliminary synthetic data simulations for the retrieval of aerosol parameters over land surfaces have been performed using the Generalized Retrieval of Aerosol and Surface Properties (GRASP) algorithm. Methods for the validation of satellite data using ground-based observations of aerosol properties are also discussed. We assume that designing, building, and launching into orbit a multi

  4. Investigating Type I Polar Stratospheric Cloud Formation Mechanisms with POAM Satellite Observations

    Science.gov (United States)

    Strawa, Anthony W.; Drdla, K.; Fromm, M.; Hoppel, K.; Browell, E.; Hamill, P.; Dempsey, D.; Gore, Warren J. (Technical Monitor)

    2001-01-01

    Type Ia PSCs are believed to be composed of nitric acid hydrate particles. Recent results from the SOLVE/THESEO 2000 campaign showed evidence that this type of PSC was composed of a small number of very large particles capable of sedimentary denitrification of regions of the stratosphere. It is unknown whether homogeneous or heterogeneous nucleation is responsible for the formation of these PSCs. Arctic winters are tending to be colder in response to global tropospheric warming. The degree to which this influences ozone depletion will depend on the freezing mechanism of nitric acid hydrate particles. If nucleation is homogeneous it implies that the freezing process is an inherent property of the particle, while heterogeneous freezing means that the extent of PSCs will depend in part on the number of nuclei available. The Polar Ozone and Aerosol Measurement (POAM)II and III satellites have been making observations of stratospheric aerosols and Polar Stratospheric Clouds (PSCs) since 1994. Recently, we have developed a technique that can discriminate between Type Ia and Ib PSCs using these observations. A statistical approach is employed to demonstrate the robustness of this approach and results are compared with lidar measurements. The technique is used to analyze observations from POAM II and II during Northern Hemisphere winters where significant PSC formation occurred with the objective of exploring Type I PSC formation mechanisms. The different PSCs identified using this method exhibit different growth curve as expressed as extinction versus temperature.

  5. Stratospheric aerosol perturbing effect on remote sensing of vegetation: Operational method for the correction of AVHRR composite NDVI

    Energy Technology Data Exchange (ETDEWEB)

    Vermote, E.; El Saleous, N. [Univ. of Maryland, College Park, MD (United States). Dept. of Geography

    1995-12-31

    In this paper the authors present an operational stratospheric aerosol correction scheme adopted by the Laboratory for Terrestrial Physics, NASA/GSFC. The stratospheric aerosol distribution is assumed to be only variable with latitude. Each 9 days the latitudinal distribution of the optical thickness is computed by inverting radiances observed in AVHRR channel 1 (0.63 microns) and channel 2 (0.83 microns) over the Pacific Ocean. This radiance data set is used to check the validity of model used for inversion by checking consistency of the optical thickness deduced from each channel as well as optical thickness deduced from different scattering angles. The deduced optical thickness and spectral dependence are compared to Mauna Loa observation from 1991 to end of 1992 for validation. Using the optical thickness profile previously computed and radiative transfer code assuming lambertian boundary condition, each pixel of channel 1 and 2 are corrected prior to computation of NDVI. Comparison between corrected, non-corrected, and years prior to Pinatubo eruption (1989, 1990) NDVI composite, shows the necessity and the accuracy of the operational correction scheme. The same technique is applied to the afternoon satellite AVHRR archive (NOAA 7, 9, 11) from 1981 to 1993. The stratospheric profile derived over ocean shows that the El Chichon eruption was of less importance than Pinatubo. The stratospheric aerosol optical depth distribution computed from AVHRR data during the El Chichon period compared well to latitudinal monthly profile based on SAGE observations.

  6. Stratospheric Water and OzOne Satellite Homogenized (SWOOSH) data set

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — The Stratospheric Water and Ozone Satellite Homogenized (SWOOSH) data set is a merged record of stratospheric ozone and water vapor measurements taken by a number of...

  7. Design and performance of the Stratospheric Aerosol and Gas Experiment II (SAGE II) instrument

    Science.gov (United States)

    Zaun, N. H.; Mauldin, L. E., III; Mccormick, M. P.

    1983-01-01

    Design and performance data are analyzed for the Stratospheric Aerosol and Gas Experiment II (SAGE II) instrument, which has been developed for the NASA Earth Radiation Budget Satellite (ERBS). SAGE II is designed to monitor globally, from 70 degrees S to 70 degrees N latitude, the vertical distribution of stratospheric aerosols, ozone, water vapor, and nitrogen dioxide by measuring the extinction of solar radiation through the earth's atmosphere during the ERBS observatory solar occultations. A flat scanning mirror reflects solar radiation into a Cassegrain type telescope, which forms a solar image on the entrance slit of a grating spectrometer. The instantaneous-field-of-view of the SAGE II is scanned along the vertical solar diameter by the elevation scan mirror. The optical system is contained within an azimuth gimbal which tracks the solar radiometric centroid during the data event, while the spectrometer isolates seven spectral wavelengths from 0.385-1.02 micrometers. The seven channels of the spectrometer use silicon photodiode dedectors operated in the photovoltaic mode. The detector outputs are multiplexed into a serial data stream for readout by the ERBS telemetry system, with each output being sampled 64 times per second and digitized to 12 bit resolution.

  8. Possible effect of extreme solar energetic particle events of September–October 1989 on polar stratospheric aerosols: a case study

    Directory of Open Access Journals (Sweden)

    I. A. Mironova

    2013-09-01

    Full Text Available The main ionization source of the middle and low Earth's atmosphere is related to energetic particles coming from outer space. Usually it is ionization from cosmic rays that is always present in the atmosphere. But in a case of a very strong solar eruption, some solar energetic particles (SEPs can reach middle/low atmosphere increasing the ionization rate up to some orders of magnitude at polar latitudes. We continue investigating such a special class of solar events and their possible applications for natural variations of the aerosol content. After the case study of the extreme SEP event of January 2005 and its possible effect upon polar stratospheric aerosols, here we analyze atmospheric applications of the sequence of several events that took place over autumn 1989. Using aerosol data obtained over polar regions from two satellites with space-borne optical instruments SAGE II and SAM II that were operating during September–October 1989, we found that an extreme major SEP event might have led to formation of new particles and/or growth of preexisting ultrafine particles in the polar stratospheric region. However, the effect of the additional ambient air ionization on the aerosol formation is minor, in comparison with temperature effect, and can take place only in the cold polar atmospheric conditions. The extra aerosol mass formed under the temperature effect allows attributing most of the changes to the "ion–aerosol clear sky mechanism".

  9. Asymmetric forcing from stratospheric aerosols impacts Sahelian rainfall

    Science.gov (United States)

    Haywood, Jim M.; Jones, Andy; Bellouin, Nicolas; Stephenson, David

    2013-07-01

    The Sahelian drought of the 1970s-1990s was one of the largest humanitarian disasters of the past 50 years, causing up to 250,000 deaths and creating 10 million refugees. It has been attributed to natural variability, over-grazing and the impact of industrial emissions of sulphur dioxide. Each mechanism can influence the Atlantic sea surface temperature gradient, which is strongly coupled to Sahelian precipitation. We suggest that sporadic volcanic eruptions in the Northern Hemisphere also strongly influence this gradient and cause Sahelian drought. Using de-trended observations from 1900 to 2010, we show that three of the four driest Sahelian summers were preceded by substantial Northern Hemisphere volcanic eruptions. We use a state-of-the-art coupled global atmosphere-ocean model to simulate both episodic volcanic eruptions and geoengineering by continuous deliberate injection into the stratosphere. In either case, large asymmetric stratospheric aerosol loadings concentrated in the Northern Hemisphere are a harbinger of Sahelian drought whereas those concentrated in the Southern Hemisphere induce a greening of the Sahel. Further studies of the detailed regional impacts on the Sahel and other vulnerable areas are required to inform policymakers in developing careful consensual global governance before any practical solar radiation management geoengineering scheme is implemented.

  10. Latitudinal and altitudinal variation of size distribution of stratospheric aerosols inferred from SAGE aerosol extinction coefficient measurements at two wavelengths

    Science.gov (United States)

    Yue, G. K.; Deepak, A.

    1984-01-01

    A method of retrieving aerosol size distribution from the measured extinction of solar radiation at wavelengths of 0.45 microns and 1.0 microns has recently been proposed. This method is utilized to obtain latitudinal and altitudinal variations of size distributions of stratospheric aerosols from the Stratospheric Aerosol and Gas Experiment data for March 1979. Small particles are found in the lower stratosphere of the tropical region, and large particles are found at higher altitudes and latitudes in both hemispheres. Results of this study are consistent with the suggestion that the upper troposphere in tropical regions is a source of condensation nuclei in the stratosphere, and they become mature as they move to higher altitudes and latitude.

  11. Likely seeding of cirrus clouds by stratospheric Kasatochi volcanic aerosol particles near a mid-latitude tropopause fold

    Science.gov (United States)

    Campbell, James R.; Welton, Ellsworth J.; Krotkov, Nickolay A.; Yang, Kai; Stewart, Sebastian A.; Fromm, Michael D.

    2012-01-01

    Following the explosive 7-8 August 2008 Mt. Kasatochi volcanic eruption in southwestern Alaska, a segment of the dispersing stratospheric aerosol layer was profiled beginning 16 August in continuous ground-based lidar measurements over the Mid-Atlantic coast of the eastern United States. On 17-18 August, the layer was displaced downward into the upper troposphere through turbulent mixing near a tropopause fold. Cirrus clouds and ice crystal fallstreaks were subsequently observed, having formed within the entrained layer. The likely seeding of these clouds by Kasatochi aerosol particles is discussed. Cloud formation is hypothesized as resulting from either preferential homogenous freezing of relatively large sulfate-based solution droplets deliquesced after mixing into the moist upper troposphere or through heterogeneous droplet activation by volcanic ash. Satellite-borne spectrometer measurements illustrate the evolution of elevated Kasatochi SO 2 mass concentrations regionally and the spatial extent of the cirrus cloud band induced by likely particle seeding. Satellite-borne polarization lidar observations confirm ice crystal presence within the clouds. Geostationary satellite-based water vapor channel imagery depicts strong regional subsidence, symptomatic of tropopause folding, along a deepening trough in the sub-tropical westerlies. Regional radiosonde profiling confirms both the position of the fold and depth of upper-tropospheric subsidence. These data represent the first unambiguous observations of likely cloud seeding by stratospheric volcanic aerosol particles after mixing back into the upper troposphere.

  12. Radicals and Aerosols in the Troposphere and Lower Stratosphere

    Science.gov (United States)

    Volkamer, Rainer; Koenig, Theodore; Dix, Barbara

    2016-06-01

    The remote tropical free troposphere (FT) is one of the most relevant atmospheric environments on Earth. About 75% of the global tropospheric O3 and CH4 loss occurs at tropical latitudes. Tropospheric bromine and iodine catalytically destroy tropospheric O3, oxidize atmospheric mercury, and modify oxidative capacity, and aerosols. Oxygenated VOCs (OVOC) modify HOx (= OH + HO2), NOx (= NO + NO2), tropospheric O3, aerosols, and are a sink for BrOx (= Br + BrO). Until recently, atmospheric models were untested for lack of vertically resolved measurements of BrO and IO radicals in the tropical troposphere. BrO and IO are highly reactive trace gases. Even very low concentrations (parts per trillion; 1 pptv = 10-12 volume mixing ratio) can significantly modify the lifetime of climate active gases, and determine (bromine) the rate limiting step of mercury oxidation in air (that is washed out, and subsequently bio-accumulates in fish). Analytical challenges arise when these radicals modify in sampling lines. Sensitive yet robust, portable, and inherently calibrated measurements directly in the open atmosphere have recently been demonstrated by means of limb-measurements of scattered solar photons by the University of Colorado Airborne Multi-AXis DOAS instrument (CU AMAX-DOAS) from research aircraft. The CU AMAX-DOAS instrument is optimized to (1) locate BrO, IO and glyoxal (a short lived OVOC) in the troposphere, (2) decouple stratospheric absorbers, (3) maximize sensitivity at instrument altitude, (4) facilitate altitude control and (5) enable observations over a wide range of solar zenith angles. Further, (6) the filling-in of Fraunhofer lines (Ring-effect) by Raman Scattering offers interesting opportunities for radiative closure studies to assess the effects of aerosols on Climate.

  13. Possible effect of extreme solar energetic particle event of 20 January 2005 on polar stratospheric aerosols: direct observational evidence

    Directory of Open Access Journals (Sweden)

    I. A. Mironova

    2011-05-01

    Full Text Available Energetic cosmic rays are the main source of ionization of the low-middle atmosphere, leading to associated changes in atmospheric properties. Via the hypothetical influence of ionization on aerosol growth and facilitated formation of cloud condensation nuclei, this may be an important indirect link relating solar variability to climate. This effect is highly debated, however, since the proposed theoretical mechanisms still remain illusive and qualitative, and observational evidence is inconclusive and controversial. Therefore, important questions regarding the existence and magnitude of the effect, and particularly the fraction of aerosol particles that can be formed and grow large enough to influence cloud condensation nuclei (CCN, are still open. Here we present empirical evidence of the possible effect caused by cosmic rays upon polar stratospheric aerosols, based on a case study of an extreme solar energetic particle (SEP event of 20 January 2005. Using aerosol data obtained over polar regions from different satellites with optical instruments that were operating during January 2005, such as the Stratospheric Aerosol and Gas Experiment III (SAGE III, and Optical Spectrograph and Infrared Imaging System (OSIRIS, we found a significant simultaneous change in aerosol properties in both the southern and northern polar regions in temporal association with the SEP event. We speculate that ionization of the atmosphere, which was abnormally high during this extreme SEP event, might have led to formation of new particles and/or growth of preexisting ultrafine particles up to the size of CCN. However, a detailed interpretation of the effect is left for subsequent studies. This is the first time high vertical resolution measurements have been used to provide evidence for the probable production of stratospheric CCN from cosmic ray induced ionization.

  14. An Empirical Method for Estimating Background Stratospheric Aerosol Extinction Profiles over China

    Institute of Scientific and Technical Information of China (English)

    2012-01-01

    The current paper introduces an empirical method for estimating the vertical distribution of background stratospheric aerosol extinction profiles covering the latitude bands of 50±5°N,40±5°N,30±5°N,and 20±5°N and the longitude range of 75 135°E based on Stratospheric Aerosol and Gas Experiment (SAGE) II aerosol extinction measurements at wavelengths of 1020 nm,525 nm,452 nm,and 386 nm for the volcanically calm years between 1998 2004.With this method,the vertical distribution of stratospheric aerosol extinction coefficients can be estimated according to latitude and wavelength.Comparisons of the empirically calculated aerosol extinction profiles and the SAGE II aerosol measurements show that the empirically calculated aerosol extinction coefficients are consistent with SAGE II values,with relative differences within 10% from 2 km above the tropopause to 33 km,and within 22% from 33 km to 35 km.The empirically calculated aerosol stratospheric optical depths (vertically integrated aerosol extinction coefficient) at the four wavelengths are also consistent with the corresponding SAGE II optical depth measurements,with differences within 2.2% in the altitude range from 2 km above the tropopause to 35 km.

  15. Response of land carbon cycle to stratospheric aerosol geoengineering

    Science.gov (United States)

    Zhang, Q.; Ji, D.

    2016-12-01

    Stabilizing the climate through geoengineering aims to mitigate the climate change induced by increasing atmospheric CO2 and other green house gases. These impacts in climate affect terrestrial ecosystem considerably because terrestrial carbon fluxes are sensitivity to climate change. Here we analyzed the responses of land carbon cycle to GeoMIP G4 experiment from six Earth System Models (ESMs), in which negative radiative forcing is produced by an injection of SO2 into the stratosphere to compensate the global warming in RCP4.5. From the year 2020 to 2090, there was an increase in land carbon uptake with significant discrepancy among models (20 PgC to 260 PgC) for both G4 and RCP4.5 scenario, due to the CO2 fertilization effect. For comparison with RCP4.5, all of the models showed higher land carbon uptakes in G4 scenario (30 Pg C on average), with both increases in vegetation and soil carbon stores. These land carbon increases relative to RCP4.5 are mainly resulted from reduced heterotrophic respiration under cooler temperature, whilst changes in vegetation productivity only account a negligible part of land carbon changes. The models also varied in their sensitivities of carbon fluxes to changes in air temperature and precipitation. Partial correlation analysis shows that interannual sensitivities of NBP to temperature and precipitation increased by 2 folds in the G4 experiment, due to higher sensitivities of NPP and Rh, yet with large differences among ESMs and spatial heterogeneity. This work suggests that stratospheric aerosol engineering would have small and positive impact on land carbon uptake but could increase climate sensitivities of terrestrial carbon fluxes significantly.

  16. Modifications of the Quasi-biennial Oscillation by a Geoengineering Perturbation of the Stratospheric Aerosol Layer

    Science.gov (United States)

    Aquila, V.; Garfinkel, C. I.; Newman, P. A.; Oman, L. D.; Waugh, D. W.

    2014-01-01

    This paper examines the impact of geoengineering via stratospheric sulfate aerosol on the quasi-biennial oscillation (QBO) using the NASA Goddard Earth Observing System (GEOS-5) Chemistry Climate Model. We performed four 30-year simulations with a continuous injection of sulfur dioxide on the equator at 0 degree longitude. The four simulations differ by the amount of sulfur dioxide injected (5Tg per year and 2.5 Tg per year) and the altitude of the injection (16km-25km and 22km-25km). We find that such an injection dramatically alters the quasi-biennial oscillation, prolonging the phase of easterly shear with respect to the control simulation. In the case of maximum perturbation, i.e. highest stratospheric aerosol burden, the lower tropical stratosphere is locked into a permanent westerly QBO phase. This locked QBO westerly phase is caused by the increased aerosol heating and associated warming in the tropical lower stratosphere.

  17. Sensitivity of Stratospheric Geoengineering with Black Carbon to Aerosol Size and Altitude of Injection

    Science.gov (United States)

    Kravitz, Ben; Robock, Alan; Shindell, Drew T.; Miller, Mark A.

    2012-01-01

    Simulations of stratospheric geoengineering with black carbon (BC) aerosols using a general circulation model with fixed sea surface temperatures show that the climate effects strongly depend on aerosol size and altitude of injection. 1 Tg BC/a injected into the lower stratosphere would cause little surface cooling for large radii but a large amount of surface cooling for small radii and stratospheric warming of over 60 C. With the exception of small particles, increasing the altitude of injection increases surface cooling and stratospheric warming. Stratospheric warming causes global ozone loss by up to 50% in the small radius case. The Antarctic shows less ozone loss due to reduction of polar stratospheric clouds, but strong circumpolar winds would enhance the Arctic ozone hole. Using diesel fuel to produce the aerosols is likely prohibitively expensive and infeasible. Although studying an absorbing aerosol is a useful counterpart to previous studies involving sulfate aerosols, black carbon geoengineering likely carries too many risks to make it a viable option for deployment.

  18. Heterogeneous chlorine activation on stratospheric aerosols and clouds in the Arctic polar vortex

    Directory of Open Access Journals (Sweden)

    T. Wegner

    2012-11-01

    Full Text Available Chlorine activation in the Arctic is investigated by examining different parameterizations for uptake coefficients on stratospheric aerosols, high-resolution in-situ measurements and vortex-wide satellite observations. The parameterizations for heterogeneous chemistry on liquid aerosols are most sensitive to temperature with the reaction rates doubling for every 1 K increase in temperature. However, differences between the currently available parameterizations are negligible. For Nitric Acid Trihydrate particles (NAT the major factors of uncertainty are the number density of nucleated particles and different parameterizations for heterogeneous chemistry. These two factors induce an uncertainty that covers several orders of magnitude on the reaction rate. Nonetheless, since predicted reaction rates on liquid aerosols always exceed those on NAT, the overall uncertainty for chlorine activation is small. In-situ observations of ClOx from Arctic winters in 2005 and 2010 are used to evaluate the heterogeneous chemistry parameterizations. The conditions for these measurements proved to be very different between those two winters with HCl being the limiting reacting partner for the 2005 measurements and ClONO2 for the 2010 measurements. Modeled levels of chlorine activation are in very good agreement with the in-situ observations and the surface area provided by Polar Stratospheric Clouds (PSCs has only a limited impact on modeled chlorine activation. This indicates that the parameterizations give a good representation of the processes in the atmosphere. Back-trajectories started on the location of the observations in 2005 indicate temperatures on the threshold for PSC formation, hence the surface area is mainly provided by the background aerosol. Still, the model shows additional chlorine activation during this time-frame, providing cautionary evidence for chlorine activation even in the absence of PSCs. Vortex-averaged satellite

  19. The STRatospheric Estimation Algorithm from Mainz (STREAM): estimating stratospheric NO2 from nadir-viewing satellites by weighted convolution

    Science.gov (United States)

    Beirle, Steffen; Hörmann, Christoph; Jöckel, Patrick; Liu, Song; Penning de Vries, Marloes; Pozzer, Andrea; Sihler, Holger; Valks, Pieter; Wagner, Thomas

    2016-07-01

    The STRatospheric Estimation Algorithm from Mainz (STREAM) determines stratospheric columns of NO2 which are needed for the retrieval of tropospheric columns from satellite observations. It is based on the total column measurements over clean, remote regions as well as over clouded scenes where the tropospheric column is effectively shielded. The contribution of individual satellite measurements to the stratospheric estimate is controlled by various weighting factors. STREAM is a flexible and robust algorithm and does not require input from chemical transport models. It was developed as a verification algorithm for the upcoming satellite instrument TROPOMI, as a complement to the operational stratospheric correction based on data assimilation. STREAM was successfully applied to the UV/vis satellite instruments GOME 1/2, SCIAMACHY, and OMI. It overcomes some of the artifacts of previous algorithms, as it is capable of reproducing gradients of stratospheric NO2, e.g., related to the polar vortex, and reduces interpolation errors over continents. Based on synthetic input data, the uncertainty of STREAM was quantified as about 0.1-0.2 × 1015 molecules cm-2, in accordance with the typical deviations between stratospheric estimates from different algorithms compared in this study.

  20. Lidar Measurements of Stratospheric Ozone, Aerosols and Temperature during the SAUNA Campaign at Sodankyla, Finland

    Science.gov (United States)

    McGee, T.; Twigg, L.; Sumnicht, G.; McPeters, R.; Bojkov, B.; Kivi, R.

    2008-01-01

    The Sodankyla Total Column Ozone Intercomparison (SAUNA) campaign took place at the Finnish Meteorological Institute Arctic Research Center (FMI-ARC) at Sodankyla, Finland (67.37 N) in two separate phases during early spring 2006, and winter 2007. These campaigns has several goals: to determine and improve the accuracy of total column ozone measurements during periods of low solar zenith angle and high total column ozone; to determine the effect of ozone profile shape on the total column retrieval; and to make validate satellite ozone measurements under these same conditions. The GSFC Stratospheric Ozone Lidar (STROZ), which makes profile measurements of ozone temperature, aerosols and water vapor participated in both phases of the campaign. During the deployments, more than 30 profile measurements were made by the lidar instrument, along with Dobson, Brewer, DOAS, ozonesonde, and satellite measurements. The presentation will concentrate on STROZ lidar results from the second phase of the campaign and comparisons with other instruments will be discussed. This will include both ground-based and satellite comparisons.

  1. Possible effect of extreme solar energetic particle events of September–October 1989 on polar stratospheric aerosols: a case study

    Directory of Open Access Journals (Sweden)

    I. A. Mironova

    2013-02-01

    Full Text Available The main ionization source of the middle and low Earth atmosphere is related to energetic particles coming from outer space. Usually it is ionization from cosmic rays that is always present in the atmosphere. But in a case of a very strong solar eruption some solar energetic particles (SEP can reach middle/low atmosphere increasing the ionization rate up to some orders of magnitude at polar latitudes. We continue investigating such a special class of solar events and their possible applications for natural variations of the aerosol content. After the case study of the extreme SEP event of January 2005 and its possible effect upon polar stratospheric aerosols, here we analyze atmospheric applications of the second sequence of several events that took place over the Autumn 1989. Using aerosol data obtained over polar regions from two satellites with space-borne optical instruments SAGE II and SAM II that were operating during September–October 1989, we found that an extreme major SEP event might have led to formation of new particles and/or growth of preexisting ultrafine particles in the polar stratospheric region. However, the effect of the additional ambient air ionization on the aerosol formation is minor, in comparison with temperature effect, and can take place only in the cold polar atmospheric conditions.

  2. Coupled aerosol-chemical modeling of UARS HNO3 and N2O5 measurements in the Arctic upper stratosphere

    Science.gov (United States)

    Bekki, S.; Chipperfield, M. P.; Pyle, J. A.; Remedios, J. J.; Smith, S. E.; Grainger, R. G.; Lambert, A.; Kumer, J. B.; Mergenthaler, J. L.

    1997-04-01

    Gas-phase photochemical models do not account for the formation of a secondary altitude HNO3 maximum in the upper stratosphere at high latitudes during winter, suggesting that some processes are missing in the currently accepted chemistry of reactive nitrogen species [Kawa et al, 1995]. Heterogeneous chemistry on aerosol particles had been discounted as the cause because the aerosol surface area is expected to be very low at these altitudes. We have coupled a sulphate aerosol microphysical model to a chemical transport model to investigate this model deficiency in the Arctic during January 1992. The aerosol model predicts the formation of small sulphate particles at 1100 K. Comparisons with cryogenic limb array etalon spectrometer (CLAES) HNO3 and improved stratospheric and mesospheric sounder (ISAMS) N2O5 observations show that the heterogeneous conversion of N2O5 to HNO3 on the modeled small sulphate particles can account for some of the unexpected features seen in Upper Atmosphere Research Satellite (UARS) observations.

  3. Numerical studies of microphysical modulations of stratospheric aerosol within ROMIC-ROSA

    Science.gov (United States)

    Hommel, René; von Savigny, Christian; Rozanov, Alexei; Burrows, John; Zalach, Jakob

    2016-04-01

    The stratospheric aerosol layer (so-called Junge layer) is an inherent part of the Brewer-Dobson circulation (BDC). Stratospheric aerosols play a large role in the Earth's climate system because they interact with catalytic cycles depleting ozone, directly alter the atmosphere's radiative balance and modulate the strength of polar vortices, in particular when this system is perturbed. In terms of mass the layer is predominantly composed of liquid sulphate-water droplets and is fed from the oxidation of gaseous precursors reaching the stratosphere either by direct volcanic injections (mainly supplying SO2) or troposphere-stratosphere exchange processes. In volcanically quiescent periods, latter processes predominantly maintain the so-called background state of aerosol layer through oxidation of OCS above 22 km, and SO2 below. The Junge layer begins to develop 2-3 km above the tropopause and reaches a height of about 35 km, with a largest vertical extent in the tropics and spring-time polar regions. Above the TTL, the layer's vertical extent varies between 2 km and 8 km (about 35% of its mean vertical expansion), depending on the phase of the QBO. The QBO-induced meridional circulation, overlying the BDC, and accompanied signatures in the stratospheric temperature directly affect the life cycle of stratospheric aerosol. Mainly by modulating the equilibrium between microphysical processes which maintain the layer. Effects caused by QBO modulations of the advective transport in the upwelling region of the BDC are smaller and difficult to quantify, because the overlying sedimentation of aerosol is also being modulated and counteract the aerosol lofting. Here we show results from numerical studies performed within the project ROMIC-ROSA (Role of Stratospheric Aerosol in Climate and Atmospheric Science). We further explored relationships between QBO forcing and aerosol processes in the lower stratosphere. We examined whether similar process interferences can be caused by

  4. Chemical analysis of refractory stratospheric aerosol particles collected within the arctic vortex and inside polar stratospheric clouds

    Science.gov (United States)

    Ebert, Martin; Weigel, Ralf; Kandler, Konrad; Günther, Gebhard; Molleker, Sergej; Grooß, Jens-Uwe; Vogel, Bärbel; Weinbruch, Stephan; Borrmann, Stephan

    2016-07-01

    Stratospheric aerosol particles with diameters larger than about 10 nm were collected within the arctic vortex during two polar flight campaigns: RECONCILE in winter 2010 and ESSenCe in winter 2011. Impactors were installed on board the aircraft M-55 Geophysica, which was operated from Kiruna, Sweden. Flights were performed at a height of up to 21 km and some of the particle samples were taken within distinct polar stratospheric clouds (PSCs). The chemical composition, size and morphology of refractory particles were analyzed by scanning electron microscopy and energy-dispersive X-ray microanalysis. During ESSenCe no refractory particles with diameters above 500 nm were sampled. In total 116 small silicate, Fe-rich, Pb-rich and aluminum oxide spheres were found. In contrast to ESSenCe in early winter, during the late-winter RECONCILE mission the air masses were subsiding inside the Arctic winter vortex from the upper stratosphere and mesosphere, thus initializing a transport of refractory aerosol particles into the lower stratosphere. During RECONCILE, 759 refractory particles with diameters above 500 nm were found consisting of silicates, silicate / carbon mixtures, Fe-rich particles, Ca-rich particles and complex metal mixtures. In the size range below 500 nm the presence of soot was also proven. While the data base is still sparse, the general tendency of a lower abundance of refractory particles during PSC events compared to non-PSC situations was observed. The detection of large refractory particles in the stratosphere, as well as the experimental finding that these particles were not observed in the particle samples (upper size limit ˜ 5 µm) taken during PSC events, strengthens the hypothesis that such particles are present in the lower polar stratosphere in late winter and have provided a surface for heterogeneous nucleation during PSC formation.

  5. Aerosol Particles From Tropical Cirrus Clouds in the Lower Stratosphere

    Science.gov (United States)

    Kojima, T.; Buseck, P. R.; Wilson, J. C.; Reeves, J. M.

    2002-12-01

    Aerosol samples were collected from convective systems and cirrus layers over Florida during the July 2002 CRYSTAL-FACE Mission. Particles between 0.02 and 700 \\micron were deposited directly onto TEM grids. Here we report preliminary results of the TEM study of particles collected near and above the tropopause. Most particles are sulfate droplets that range from 0.8 to 5 \\micron in diameter on the TEM grids. All have a characteristic appearance that consists of a main central particle (0.3 -1 \\micron) surrounded by many smaller satellite droplets. Their appearance suggests that the droplets were sulfuric acid partially neutralized with ammonium at the time of collection, with ammonium sulfate and bisulfate constituting the central particles (Bigg, 1975, 1980). The degree of ammoniation in individual droplets, which is indicated by the size of central particles relative to satellite ring diameter, is fairly uniform. The ratio of central particle diameter to satellite ring diameter is generally around 0.3. Such ammoniated droplets with solid cores may be more efficient in nucleating cirrus than pure sulfuric acid droplets (Tabazadeh and Toon, 1998). Ammonium sulfate particles without satellites commonly coexist with the acid droplets. Minor particles consist of C-rich amorphous material, silicates, Na- and K-chlorides and sulfates, and Cr- and Ti-oxides. Some were coated with sulfate. Many of the C-rich particles contain significant amount of K, S, and O with lesser N. All silicate particles are flakes of clay minerals that have pseudohexagonal structures. They would work as effective ice nuclei (Pruppacher and Klett, 1997).

  6. Analysis of stratospheric NO2 trends above Jungfraujoch using ground-based UV-visible, FTIR, and satellite nadir observations

    Directory of Open Access Journals (Sweden)

    R. Stübi

    2012-09-01

    Full Text Available The trend in stratospheric NO2 column at the NDACC (Network for the Detection of Atmospheric Composition Change station of Jungfraujoch (46.5° N, 8.0° E is assessed using ground-based FTIR and zenith-scattered visible sunlight SAOZ measurements over the period 1990 to 2009 as well as a composite satellite nadir data set constructed from ERS-2/GOME, ENVISAT/SCIAMACHY, and METOP-A/GOME-2 observations over the 1996–2009 period. To calculate the trends, a linear least squares regression model including explanatory variables for a linear trend, the mean annual cycle, the quasi-biennial oscillation (QBO, solar activity, and stratospheric aerosol loading is used. For the 1990–2009 period, statistically indistinguishable trends of −3.7 ± 1.1% decade−1 and −3.6 ± 0.9% decade−1 are derived for the SAOZ and FTIR NO2 column time series, respectively. SAOZ, FTIR, and satellite nadir data sets show a similar decrease over the 1996–2009 period, with trends of −2.4 ± 1.1% decade−1, −4.3 ± 1.4% decade−1, and −3.6 ± 2.2% decade−1, respectively. The fact that these declines are opposite in sign to the globally observed +2.5% decade−1 trend in N2O, suggests that factors other than N2O are driving the evolution of stratospheric NO2 at northern mid-latitudes. Possible causes of the decrease in stratospheric NO2 columns have been investigated. The most likely cause is a change in the NO2/NO partitioning in favor of NO, due to a possible stratospheric cooling and a decrease in stratospheric chlorine content, the latter being further confirmed by the negative trend in the ClONO2 column derived from FTIR observations at Jungfraujoch. Decreasing ClO concentrations slows the NO + ClO → NO2 + Cl reaction and a stratospheric cooling slows the NO + O3 → NO2 + O2 reaction, leaving more NOx in the form of NO. The slightly positive trends in ozone estimated from ground- and satellite-based data sets are also consistent with the decrease of

  7. Analysis of stratospheric NO2 trends above Jungfraujoch using ground-based UV-visible, FTIR, and satellite nadir observations

    Directory of Open Access Journals (Sweden)

    R. Stübi

    2012-05-01

    Full Text Available The trend in stratospheric NO2 column at the NDACC (Network for the Detection of Atmospheric Composition Change station of Jungfraujoch (46.5° N, 8.0° E is assessed using ground-based FTIR and zenith-scattered visible sunlight SAOZ measurements over the period 1990 to 2009 as well as a composite satellite nadir data set constructed from ERS-2/GOME, ENVISAT/SCIAMACHY, and METOP-A/GOME-2 observations over the 1996–2009 period. To calculate the trends, a linear least squares regression model including explanatory variables for a linear trend, the mean annual cycle, the quasi-biennial oscillation (QBO, solar activity, and stratospheric aerosol loading is used. For the 1990–2009 period, statistically indistinguishable trends of −3.7 ± 1.1%/decade and −3.6 ± 0.9%/decade are derived for the SAOZ and FTIR NO2 column time series, respectively. SAOZ, FTIR, and satellite nadir data sets show a similar decrease over the 1996–2009 period, with trends of −2.4 ± 1.1%/decade, −4.3 ± 1.4%/decade, and −3.6 ± 2.2%/decade, respectively. The fact that these declines are opposite in sign to the globally observed +2.5%/decade trend in N2O, suggests that factors other than N2O are driving the evolution of stratospheric NO2 at northern mid-latitudes. Possible causes of the decrease in stratospheric NO2 columns have been investigated. The most likely cause is a change in the NO2/NO partitioning in favor of NO, due to a possible stratospheric cooling and a decrease in stratospheric chlorine content, the latter being further confirmed by the negative trend in the ClONO2 column derived from FTIR observations at Jungfraujoch. Decreasing ClO concentrations slows the NO + ClO → NO2 + Cl reaction and a stratospheric cooling slows the NO + O3 → NO2 + O2 reaction, leaving more NOx in the form of NO. The slightly positive trends in ozone estimated from ground- and satellite-based data sets are also consistent with the decrease of NO2 through the NO2 + O3

  8. Stratospheric aerosol acidity, density, and refractive index deduced from SAGE 2 and NMC temperature data

    Science.gov (United States)

    Yue, G. K.; Poole, L. R.; Wang, P.-H.; Chiou, E. W.

    1994-01-01

    Water vapor concentrations obtained by the Stratospheric Aerosol and Gas Experiment 2 (SAGE 2) and collocated temperatures provided by the National Meteorological Center (NMC) from 1986 to 1990 are used to deduce seasonally and zonally averaged acidity, density, and refractive index of stratospheric aerosols. It is found that the weight percentage of sulfuric acid in the aerosols increases from about 60 just above the tropopause to about 86 at 35 km. The density increases from about 1.55 to 1.85 g/cu cm between the same altitude limits. Some seasonal variations of composition and density are evident at high latitudes. The refractive indices at 1.02, 0.694, and 0.532 micrometers increase, respectively, from about 1.425, 1.430, and 1.435 just above the tropopause to about 1.445, 1.455, and 1.458 at altitudes above 27 km, depending on the season and latitude. The aerosol properties presented can be used in models to study the effectiveness of heterogeneous chemistry, the mass loading of stratospheric aerosols, and the extinction and backscatter of aerosols at different wavelengths. Computed aerosol surface areas, rate coefficients for the heterogeneous reaction ClONO2 + H2O yields HOCl + HNO3 and aerosol mass concentrations before and after the Pinatubo eruption in June 1991 are shown as sample applications.

  9. On geoengineering with sulphate aerosols in the tropical upper troposphere and lower stratosphere

    Energy Technology Data Exchange (ETDEWEB)

    Tuck, A.F. [NOAA Earth System Research Laboratory, Boulder, CO (United States); Donaldson, D.J. [University of Toronto, Ontario (Canada); Hitchman, M.H. [University of Wisconsin, Madison, WI (United States); Richard, E.C. [University of Colorado, Boulder, CO (United States). Laboratory for Atmospheric and Space Physics; Tervahattu, H. [Nordic Envicon Oy, Helsinki (Finland); Vaida, V. [University of Colorado, Boulder, CO (United States). Department of Chemistry and Biochemistry; Wilson, J.C. [University of Denver, Denver, CO (United States). Department of Engineering

    2008-10-15

    This paper is in response to the Editorial Essay by Crutzen and the Editorial Comment by Cicerone in the August 2006 issue of Climatic Change. We reprise the evidence from atmospheric nuclear weapon testing in the 1950s and 1960s which is salient to the mooted maintenance of an artificial sulphate aerosol layer in the lower stratosphere, including a hitherto and now posthumous unpublished analysis of the {sup 185}W Hardtack data. We also review recent investigations by ourselves, which have considerable bearing on some relevant questions concerning meteorological dynamics, aerosol chemistry and physics and the photodissociation of stratospheric sulphuric acid.

  10. Lidar measurements of stratospheric aerosols from Mount Pinatubo at Camaguey, Cuba

    Science.gov (United States)

    Antuña, Juan Carlos

    Lidar measurements of stratospheric aerosols made at Camaguey, Cuba 21°N, six months after Mount Pinatubo eruption, show a very large increase in the stratospheric aerosol burden. Peak scattering ratios greater than 20 have been observed in early January 1992. In the same month integrated backscattering in the layer between 16 and 33 km shows a maximum value larger than 5 × 10 -3 sr -1. The course of those parameters such as the height of peaks and of the layer base between January 1992 and November 1993 is shown.

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

    Science.gov (United States)

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

    1989-01-01

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

  12. Lidar Observation of the 2014 Kelut Volcanic Stratospheric Aerosols at Kototabang, Indonesia

    Science.gov (United States)

    Abo, Makoto; Shibata, Yasukuni; Nagasawa, Chikao

    2016-06-01

    The Kelut (Kelud) volcano (7.9S, 112.3E) in the Java island of Indonesia erupted on 13 February 2014. The CALIOP observed that the eruption cloud reached 26km above sea level. We have observed this stratospheric aerosol from 28 February 2014 at equatorial lidar site located in the Sumatra island of Indonesia (0.2S, 100.3E). We observed the depolarization maximum to be up to 2km below the backscatter maximum in April 2014. We also observed the vertical transportation process of stratospheric aerosol to troposphere by equatorial Kelvin wave.

  13. Odin-OSIRIS stratospheric aerosol data product and SAGE III intercomparison

    Directory of Open Access Journals (Sweden)

    A. E. Bourassa

    2012-01-01

    Full Text Available The scattered sunlight measurements made by the Optical Spectrograph and InfraRed Imaging System (OSIRIS on the Odin spacecraft are used to retrieve vertical profiles of stratospheric aerosol extinction at 750 nm. The recently released OSIRIS Version 5 data product contains the first publicly released stratospheric aerosol extinction retrievals, and these are now available for the entire Odin mission, which extends from the present day back to launch in 2001. A proof-of-concept study for the retrieval of stratospheric aerosol extinction from limb scatter measurements was previously published and the Version 5 data product retrievals are based on this work, but incorporate several important improvements to the algorithm. One of the primary changes is the use of a new retrieval vector that greatly improves the sensitivity to aerosol scattering by incorporating a forward modeled calculation of the radiance from a Rayleigh atmosphere. Additional improvements include a coupled retrieval of the effective albedo, a new method for normalization of the retrieval vector to improve signal-to-noise, and the use of an initial guess that is representative of very low background aerosol loading conditions, which allows for maximal retrieval range. Furthermore, the Version 5 data set is compared to Stratospheric Aerosol and Gas Experiment (SAGE III 755 nm extinction profiles during the almost four years of mission overlap from 2002 to late 2005. The vertical structure in coincident profile measurements is well correlated and the statistics on a relatively large set of tight coincident measurements show agreement between the measurements from the two instruments to within approximately 10% throughout the 15 to 25 km altitude range, which covers the bulk of the stratospheric aerosol layer for the mid and high latitude cases studied here.

  14. On recent (2008–2012 stratospheric aerosols observed by lidar over Japan

    Directory of Open Access Journals (Sweden)

    O. Uchino

    2012-12-01

    Full Text Available An increase in stratospheric aerosols caused by the volcanic eruption of Mt. Nabro (13.37° N, 41.70° E on 12 June 2011 was detected by lidar at Tsukuba (36.05° N, 140.13° E and Saga (33.24° N, 130.29° E in Japan. The maximum backscattering ratios at a wavelength of 532 nm were 2.0 at 17.0 km on 10 July 2011 at Tsukuba and 3.6 at 18.2 km on 23 June 2011 at Saga. The maximum integrated backscattering coefficients (IBCs at 532 nm above the first tropopause height were 4.18×10−4 sr−1 on 11 February 2012 at Tsukuba and 4.19×10−4 sr−1 on 23 June 2011 at Saga, respectively.

    A time series of lidar observational results at Tsukuba have also been reported from January 2008 through May 2012. Increases in stratospheric aerosols were observed after the volcanic eruptions of Mt. Kasatochi (52.18° N, 175.51° E in August 2008 and Mt. Sarychev Peak (48.09° N, 153.20° E in June 2009. The yearly averaged IBCs at Tsukuba were 2.54×10−4 sr−1, 2.48×10−4 sr−1, 2.45×10−4 sr−1, and 2.20×10−4 sr−1 for 2008, 2009, 2010, and 2011, respectively. These values were about twice the IBC background level (1.21×10−4 sr−1 from 1997 to 2001 at Tsukuba. We briefly discuss the influence of the increased aerosols on climate and the implications for analysis of satellite data.

  15. Evolution of stratospheric ozone and water vapour time series studied with satellite measurements

    Directory of Open Access Journals (Sweden)

    A. Jones

    2009-01-01

    Full Text Available The long term evolution of stratospheric ozone and water vapour has been investigated by extending satellite time series to April 2008. For ozone, we examine monthly average ozone values from various satellite data sets for nine latitude and altitude bins covering 60° S to 60° N and 20–45 km and covering the time period 1979–2008. Data are from the Stratospheric Aerosol and Gas Experiment (SAGE I+II, the HALogen Occultation Experiment (HALOE, the Solar BackscatterUltraViolet-2 (SBUV/2 instrument, the Sub-Millimetre Radiometer (SMR, the Optical Spectrograph InfraRed Imager System (OSIRIS, and the SCanning Imaging Absorption spectroMeter for Atmospheric CHartograpY (SCIAMACHY. Monthly ozone anomalies are calculated by utilising a linear regression model, which also models the solar, quasi-biennial oscillation (QBO, and seasonal cycle contributions. Individual instrument ozone anomalies are combined producing a weighted all instrument average. Assuming a turning point of 1997 and that the all instrument average is represented by good instrumental long term stability, the largest statistically significant ozone declines from 1979–1997 are seen at the mid-latitudes between 35 and 45 km, namely −7.7%/decade in the Northern Hemisphere and −7.8%/decade in the Southern Hemisphere. For the period 1997 to 2008 we find that the southern mid-latitudes between 35 and 45 km show the largest ozone recovery (+3.4%/decade compared to other global regions, although the estimated trend model error is of a similar magnitude (+2.1%/decade, at the 95% confidence level. An all instrument average is also constructed from water vapour anomalies during 1984–2008, using the SAGE II, HALOE, SMR, and the Microwave Limb Sounder (aura/MLS measurements. We report that the decrease in water vapour values after 2001 slows down around 2004 in the lower tropical stratosphere (20–25 km, and has even shown signs of increasing values in upper stratospheric mid

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

    Science.gov (United States)

    Thomason, L. W.

    2012-01-01

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

  17. Coherent Evaluation of Aerosol Data Products from Multiple Satellite Sensors

    Science.gov (United States)

    Ichoku, Charles

    2011-01-01

    Aerosol retrieval from satellite has practically become routine, especially during the last decade. However, there is often disagreement between similar aerosol parameters retrieved from different sensors, thereby leaving users confused as to which sensors to trust for answering important science questions about the distribution, properties, and impacts of aerosols. As long as there is no consensus, and the inconsistencies are not well characterized and understood, there will be no way of developing reliable model inputs and climate data records from satellite aerosol measurements. Fortunately, the Aerosol Robotic Network (AERONET) is providing well-calibrated globally representative ground-based aerosol measurements corresponding to the satellite-retrieved products. Through a recently developed web-based Multi-sensor Aerosol Products Sampling System (MAPSS), we are utilizing the advantages offered by collocated AERONET and satellite products to characterize and evaluate aerosol retrieval from multiple sensors. Indeed, MAPSS and its companion statistical tool AeroStat are facilitating detailed comparative uncertainty analysis of satellite aerosol measurements from Terra-MODIS, Aqua-MODIS, Terra-MISR, Aura-OMI, Parasol-POLDER, and Calipso-CALIOP. In this presentation, we will describe the strategy of the MAPSS system, its potential advantages for the aerosol community, and the preliminary results of an integrated comparative uncertainly analysis of aerosol products from multiple satellite sensors.

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

    Science.gov (United States)

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

    2013-12-01

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

  19. Interpretation of DIAL Measurements of Lower Stratospheric Ozone in Regions with Pinatubo Aerosols

    Science.gov (United States)

    Grant, William B.; Browell, Edward V.; Fenn, Marta A.; Butler, Carolyn F.; Brackett, Vincent G.; Veiga, Robert E.; Mayor, Shane D.; Fishman, Jack; Nganga, D.; Minga, A.

    1992-01-01

    The influence of volcanic aerosols on stratospheric ozone is a topic of current interest, especially with the June 15, 1991 eruption of Mt. Pinatubo in the Philippines. Lidar has been used in the past to provide aerosol profiles which could be compared with ozone profiles measured using ozonesondes to look for coincidences between volcanic aerosols and ozone decreases. The differential absorption lidar (DIAL) technique has the advantages of being able to measure ozone and aerosol profiles simultaneously as well as being able to cover large geographical regions rapidly. While there are problems associated with correcting the ozone profiles for the presence of aerosols, the corrections can be made reliably when the wavelengths are closely spaced and the Bernoulli method is applied. The DIAL measurements considered in this paper are those obtained in the tropical stratosphere in January 1992 during the Airborne Arctic Stratospheric Expedition (AASE-II). The determination of ozone profiles in the presence of Pinatubo aerosols is discussed in a companion paper.

  20. Assessing the direct occupational and public health impacts of solar radiation management with stratospheric aerosols.

    Science.gov (United States)

    Effiong, Utibe; Neitzel, Richard L

    2016-01-19

    Geoengineering is the deliberate large-scale manipulation of environmental processes that affects the Earth's climate, in an attempt to counteract the effects of climate change. Injecting sulfate aerosol precursors and designed nanoparticles into the stratosphere to (i.e., solar radiation management [SRM]), has been suggested as one approach to geoengineering. Although much is being done to unravel the scientific and technical challenges around geoengineering, there have been few efforts to characterize the potential human health impacts of geoengineering, particularly with regards to SRM approaches involving stratospheric aerosols. This paper explores this information gap. Using available evidence, we describe the potential direct occupational and public health impacts of exposures to aerosols likely to be used for SRM, including environmental sulfates, black carbon, metallic aluminum, and aluminum oxide aerosols. We speculate on possible health impacts of exposure to one promising SRM material, barium titanate, using knowledge of similar nanomaterials. We also explore current regulatory efforts to minimize exposure to these toxicants. Our analysis suggests that adverse public health impacts may reasonably be expected from SRM via deployment of stratospheric aerosols. Little is known about the toxicity of some likely candidate aerosols, and there is no consensus regarding acceptable levels for public exposure to these materials. There is also little infrastructure in place to evaluate potential public health impacts in the event that stratospheric aerosols are deployed for solar radiation management. We offer several recommendations intended to help characterize the potential occupation and public health impacts of SRM, and suggest that a comprehensive risk assessment effort is needed before this approach to geoengineering receives further consideration.

  1. Determination of atmospheric aerosol properties over land using satellite measurements

    NARCIS (Netherlands)

    Kokhanovsky, A.A.; Leeuw, G. de

    2009-01-01

    Mostly, aerosol properties are poorly understood because the aerosol properties are very sparse. The first workshop on the determination of atmospheric aerosol properties over land using satellite measurements is convened in Bremen, Germany. In this workshop, the topics of discussions included a var

  2. Aerosol-associated changes in tropical stratospheric ozone following the eruption of Mount Pinatubo

    Science.gov (United States)

    Grant, William B.; Browell, Edward V.; Fishman, Jack; Brackett, Vincent G.; Veiga, Robert E.; Nganga, Dominique; Minga, A.; Cros, Bernard; Butler, Carolyn F.; Fenn, Marta A.

    1994-01-01

    The large amount of sulfuric acid aerosol formed in the stratosphere by conversion of sulfur dioxide emitted by the eruption of Mount Pinatubo (15.14 deg N, 120.35 deg E) in the Philippines around June 15, 1991, has had a pronounced effect on lower stratospheric ozone in the tropics. Measurements of stratospheric ozone in the tropics using electrochemical concentration cell (ECC) sondes before and after the eruption and the airborne UV differential absorption lidar (DIAL) system after the eruption are compared with Stratospheric Aerosol and Gas Experiment II (SAGE II) measurements from several years before the eruption and ECC sonde measurements from the year prior to the eruption to determine the resulting changes. Ozone decreases of up to 33 % compared with SAGE II climatological values were found to be directly correlated with altitude regions of enhanced aerosol loading in the 16- to 28-km range. A maximum partial-column decrease of 29 +/- Dobson units (DU) was found over the 16- to 28-km range in September 1991 along with small increases (to 5.9 +/- 2 DU) from 28 to 31.5 km. A large decrease of ozone was also found at 4 deg to 8 deg S from May to August 1992, with a maximum decrease of 33 +/- 7 DU found above Brazzaville in July. Aerosol data form the visible channel of the advanced very high resolution radiometer (AVHRR) and the visible wavelength of the UV DIAL system were used to examine the relationship between aerosol (surface area) densities and ozone changes. The tropical stratospheric ozone changes we observed in 1991 and 1992 are likely be explained by a combination of dynamical (vertical transport) perturbations, radiative perturbations on ozone photochemistry, and heterogeneous chemistry.

  3. NUMBER CONCENTRATION, SIZE DISTRIBUTION AND FINE PARTICLE FRACTION OF TROPOSPHERIC AND STRATOSPHERIC AEROSOLS

    Institute of Scientific and Technical Information of China (English)

    Li Xu; Guangyu Shi; Li Zhang; Jun Zhou; Yasunobu Iwasaka

    2003-01-01

    Aerosol observations were carried out at Xianghe Scientific Balloon Base (39.45°N, 117°E) using a stratospheric balloon. The particle number concentrations of the tropospheric and stratospheric aerosols were directly explored.The vertical distributions of the number concentration, number-size (that is, particle number versus particle size)distribution, and the fraction of fine particles (0.5 μm>r>0.15 μm/r>0.15 μm) are reported in this paper. The profiles of particle concentration present multi-peak phenomenon. The pattern of size distribution for atmospheric aerosol indicates a tri-modal (r=~0.2 μm, ~0.88 μm and ~7.0 μm) and a bi-modal (r=~0.13 μm and 2.0 μm). The number-size distribution almost fits the Junge distribution for particles with r<0.5 μm in the stratosphere of 1993 and the troposphere of 1994. But the distributions of coarse particles (r>0.5 μm) are not uniform. The number-size distribution exhibits also a wide size range in the troposphere of 1993. The results demonstrate that fine particles represent the major portion in the troposphere during the measurement period, reaching as high as 95% in 1994. Certain coarse particle peaks in the troposphere were attributed to clouds and other causes, and in the stratosphere to volcanic eruption. The stratospheric aerosol layer consists of unique fractions of fine or coarse particles depending on their sources. In summary, the process of gas-to-particles conversion was active and the coarse particles were rich over the Xianghe area. The measurements also demonstrate that the spatial and temporal atmospheric aerosol distributions are nonuniform and changeful.

  4. Long-Term Variation of Stratospheric Aerosols Observed With Lidar from 1982 to 2014 Over Tsukuba, Japan

    Science.gov (United States)

    Sakai, Tetsu; Uchino, Osamu; Nagai, Tomohiro; Fujimoto, Toshifumi; Tabata, Isao

    2016-06-01

    The vertical distribution of stratospheric aerosols has been measured with lidars at the Meteorological Research Institute (MRI) over Tsukuba since 1982. After two major volcanic eruptions (Mt. El Chichón in 1982 and Mt. Pinatubo in 1991), stratospheric aerosol loading increased about 50-100 times compared with the background level which was observed for 1997-2000. From 2000 to 2012, a slight increase (5.3% year-1) was observed by some volcanic eruptions. This long-term lidar data have been used for assessing of impact of the stratospheric aerosols on climate and the ozone layer.

  5. Volcanic-aerosol-induced changes in stratospheric ozone following the eruption of Mount Pinatubo

    Science.gov (United States)

    Grant, W. B.; Browell, E. V.; Fishman, J.; Brackett, V. G.; Fenn, M. A.; Butler, C. F.; Nganga, D.; Minga, A.; Cros, B.; Mayor, S. D.

    1994-01-01

    Measurements of lower stratospheric ozone in the Tropics using electrochemical concentrations cell (ECC) sondes and the airborne UV Differential Absorption Lidar (DIAL) system after the eruption of Mt. Pinatubo are compared with the Stratospheric Aerosol and Gas Experiment 2 (SAGE 2) and ECC sonde measurements from below the eruption to determine what changes have occurred as a result. Aerosol data from the Advanced Very High Resolution Radiometer (AVHRR) and the visible and IR wavelengths of the lidar system are used to examine the relationship between aerosols and ozone changes. Ozone decreases of 30 percent at altitudes between 19 and 26 km, partial column (16-28 km) decreases of about 27 D.U., and slight increases (5.4 D.U.) between 28 and 31 km are found in comparison with SAGE 2 climatological values.

  6. Meteoric smoke and H2SO4 aerosols in the upper stratosphere and mesosphere

    Science.gov (United States)

    Hervig, Mark E.; Bardeen, Charles G.; Siskind, David E.; Mills, Michael J.; Stockwell, Robert

    2017-01-01

    Meteoric smoke has traditionally been understood as a passive tracer which follows the global mesospheric circulation. Smoke extinction measured by the Solar Occultation For Ice Experiment, however, shows that while this is true in the middle to upper mesosphere (pressure hPa), it is not true near the stratopause. Here the expected winter increase begins 3 months earlier than in models. We suggest that the autumn extinction increase is due to H2SO4 condensing above the nominal stratospheric aerosol layer ( 5 hPa). This is possible due to lowering of the H2SO4 saturation vapor pressure when the acid is neutralized through combination with meteoric metals. The appearance of neutralized H2SO4 aerosol in autumn is associated with the seasonal decrease in temperature. The combination of meteoric smoke and neutralized H2SO4 aerosols explains the observations and supports previous suggestions that H2SO4 could condense above the nominal stratospheric sulfate layer.

  7. Fluorescence from atmospheric aerosol detected by a lidar indicates biogenic particles in the lowermost stratosphere

    Directory of Open Access Journals (Sweden)

    F. Immler

    2005-01-01

    Full Text Available With a lidar system that was installed in Lindenberg/Germany, we observed in June 2003 an extended aerosol layer at 13km altitude in the lowermost stratosphere. This layer created an inelastic backscatter signal that we detected with a water vapour Raman channel, but that was not produced by Raman scattering. Also, we find evidence for inelastic scattering from a smoke plume from a forest fire that we observed in the troposphere. We interpret the unexpected properties of these aerosols as fluorescence induced by the laser beam at organic components of the aerosol particles. Fluorescence from ambient aerosol had not yet been considered detectable by lidar systems. However, organic compounds such as polycyclic aromatic hydrocarbons sticking to the aerosol particles, or bioaerosol such as bacteria, spores or pollen fluoresce when excited with UV-radiation in a way that is detectable by our lidar system. Therefore, we conclude that fluorescence from organic material released by biomass burning creates, inelastic backscatter signals that we measured with our instrument and thus demonstrate a new and powerful way to characterize aerosols by a remote sensing technique. The stratospheric aerosol layer that we have observed in Lindenberg for three consecutive days is likely to be a remnant from Siberian forest fire plumes lifted across the tropopause and transported around the globe.

  8. Odin-OSIRIS stratospheric aerosol data product and SAGE III intercomparison

    Directory of Open Access Journals (Sweden)

    A. E. Bourassa

    2011-09-01

    Full Text Available The scattered sunlight measurements made by the Optical Spectrograph and InfraRed Imaging System (OSIRIS on the Odin spacecraft are used to retrieve vertical profiles of stratospheric aerosol extinction at 750 nm. The recently released OSIRIS Version 5 data product contains the first publicly released stratospheric aerosol extinction retrievals, and these are now available for the entire Odin mission, which extends from the present day back to launch in 2001. A proof-of-concept study for the retrieval of stratospheric aerosol extinction from limb scatter measurements was previously published and the Version 5 data product retrievals are based on this work, but incorporate several important improvements to the algorithm. One of the primary changes is the use of a new retrieval vector that greatly improves the sensitivity to aerosol scattering by incorporating a forward modeled calculation of the radiance from a Rayleigh atmosphere. Additional improvements include a coupled retrieval of the effective albedo, a new method for normalization of the measurement vector to improve signal-to-noise, and the use of an initial guess that is representative of very low background aerosol loading conditions, which allows for maximal retrieval range. Furthermore, the Version 5 data set is compared to SAGE III 755 nm extinction profiles during the almost four years of mission overlap from 2002 to late 2005. The vertical structure in coincident profile measurements is well correlated and the statistics on a relatively large set of tight coincident measurements show agreement between the measurements from the two instruments to within approximately 10 % throughout the 15 to 25 km altitude range, which covers the bulk of the stratospheric aerosol layer for the mid and high latitude cases studied here.

  9. Evolution of stratospheric ozone and water vapour time series studied with satellite measurements

    Directory of Open Access Journals (Sweden)

    A. Jones

    2009-08-01

    Full Text Available The long term evolution of stratospheric ozone and water vapour has been investigated by extending satellite time series to April 2008. For ozone, we examine monthly average ozone values from various satellite data sets for nine latitude and altitude bins covering 60° S to 60° N and 20–45 km and covering the time period of 1979–2008. Data are from the Stratospheric Aerosol and Gas Experiment (SAGE I+II, the HALogen Occultation Experiment (HALOE, the Solar BackscatterUltraViolet-2 (SBUV/2 instrument, the Sub-Millimetre Radiometer (SMR, the Optical Spectrograph InfraRed Imager System (OSIRIS, and the SCanning Imaging Absorption spectroMeter for Atmospheric CHartograpY (SCIAMACHY. Monthly ozone anomalies are calculated by utilising a linear regression model, which also models the solar, quasi-biennial oscillation (QBO, and seasonal cycle contributions. Individual instrument ozone anomalies are combined producing an all instrument average. Assuming a turning point of 1997 and that the all instrument average is represented by good instrumental long term stability, the largest statistically significant ozone declines (at two sigma from 1979–1997 are seen at the mid-latitudes between 35 and 45 km, namely −7.2%±0.9%/decade in the Northern Hemisphere and −7.1%±0.9%/in the Southern Hemisphere. Furthermore, for the period 1997 to 2008 we find that the same locations show the largest ozone recovery (+1.4% and +0.8%/decade respectively compared to other global regions, although the estimated trend model errors indicate that the trend estimates are not significantly different from a zero trend at the 2 sigma level. An all instrument average is also constructed from water vapour anomalies during 1991–2008, using the SAGE II, HALOE, SMR, and the Microwave Limb Sounder (Aura/MLS measurements. We report that the decrease in water vapour values after 2001 slows down around 2004–2005 in the lower tropical stratosphere (20–25 km and has even

  10. Fluorescence from atmospheric aerosol detected by a lidar indicates biogenic particles in the stratosphere

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    F. Immler

    2004-09-01

    Full Text Available With a lidar system that was installed in Lindenberg/Germany, we observed in June 2003, an extended aerosol layer at 13 km altitude in the lowermost stratosphere. This layer created an inelastic backscatter signal which we interpret as laser induced fluorescence from aerosol particles. Also, we find evidence for inelastic scattering in a smoke plume from a forest fire that we observed in the troposphere. Fluorescence from ambient aerosol had not yet been considered detectable by lidar. However, organic compounds such as polycyclic aromatic hydrocarbons sticking to the aerosol particles, or bioaerosol such as bacteria, spores or pollen fluoresce when excited with UV-radiation in a way that is detectable by our lidar system. Therefore, we conclude that fluorescence from organic material released by biomass burning creates the inelastic backscatter signal that we measured with our instrument and thus demonstrate a new and powerful way to characterize aerosols by a remote sensing technique. The stratospheric aerosol layer that we have observed in Lindenberg for three consecutive days is likely to be a remnant from Siberian forest fire plumes lifted across the tropopause and transported around the globe.

  11. Balloon-borne observations of stratospheric aerosol in Antarctica from 1972 to 1984

    Science.gov (United States)

    Hofmann, D. J.

    1985-01-01

    Stratospheric levels of particles with r or = 0.15 microns were monitored with optical particle counters in approximately monthly balloon soundings at Laramie, Wyoming (41 deg N) since 1971. These measurements were used to characterize the background stratospheric aerosol layer and the disturbed layer following major volcanic eruptions. Levels of particles with r or = 0.01 microns have also been measured with balloon-borne counters since 1973. The latter are collectively called condensation nuclei (CN) as they are characteristic of aerosol in the early stages of growth. While they dominate the size distribution in the tropsophere, they are a trace species in the undisturbed stratosphere. From 1972 until 1980, annual balloon soundings from McMurdo Station (78 deg S) and/or Amundsen-Scott Station (90 deg S), in Antarctica, have also been conducted to crudely monitor Southern Hemisphere aerosol levels. These measurements were continued in 1983 and 1984. Profiles of r 0.15 microns aerosol concentrations as measured during January at the south pole from 1972 to 1975 and in 1980 are given. The former are typical of undisturbed conditions and indicate the small degree of variability under these conditions. The latter indicates the effect of minor volcanic activity, visible in the 10 to 15 km region.

  12. Toward a combined SAGE II-HALOE aerosol climatology: an evaluation of HALOE version 19 stratospheric aerosol extinction coefficient observations

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    L. W. Thomason

    2012-09-01

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

  13. Retrieval Of Stratospheric Aerosol Properties From Sciamachy Limb Observations

    Science.gov (United States)

    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.

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

    Science.gov (United States)

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

    2014-01-01

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

  15. Use of satellite data and modeling to asses the influence of stratospheric processes on the troposphere

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    Nathan, Terrence R.; Yarger, Douglas N.

    1989-01-01

    The research is comprised of the following tasks: use of simple analytical and numerical models of a coupled troposphere-stratosphere system to examine the effects of radiation and ozone on planetary wave dynamics and the tropospheric circulation; use of satellite data obtained from the Nimbus 7 Limb Infrared Monitor of the Stratosphere (LIMS) instrument and Solar Backscattered Ultraviolet (SBUV) experiment, in conjunction with National Meteorological Center (NMC) data, to determine the planetary wave vertical structures, dominant wave spectra, ozone spectra, and time variations in diabatic heating rate; and synthesis of the modeling and observational results to provide a better understanding of the effects that stratospheric processes have on tropospheric dynamics.

  16. The effect of volcanic aerosols on the thermal infrared budget of the lower stratosphere

    Science.gov (United States)

    Charlock, T. P.

    1983-01-01

    The thermal IR heating of the stratosphere due to volcanic aerosols such as those released by the eruption of El Chichon is investigated by means of clear-sky model computations using a LOWTRAN5 radiance code (Kneizys et al., 1980) modified by Charlock (1983) to increase its vertical resolution. The results are presented graphically for 4-km-thick aerosol layers at altitudes 18, 22, and 25 km and at latitudes 0 deg and 35 deg N, and the effects of tropospheric cloud height (0-10 km) are taken into account. The aerosol-induced IR divergence is shown to depend on aerosol height and to be highly and nonlinearly sensitive to the location of underlying water clouds.

  17. Infrared limb emission measurements of aerosol in the troposphere and stratosphere

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    S. Griessbach

    2015-04-01

    Full Text Available Altitude resolved aerosol detection in the upper troposphere and lower stratosphere (UTLS is a challenging task for remote sensing instruments. Here, we introduce a new method for detecting aerosol in the UTLS based on infrared limb emission measurements. The method applies an improved aerosol-cloud-index that indicates infrared limb spectra affected by aerosol and ice clouds. For the discrimination between aerosol and ice clouds we developed a new method based on brightness temperature difference correlations. The discrimination thresholds for the new method were derived from radiative transfer simulations (including scattering and Michelson Interferometer for Passive Atmospheric Sounding (MIPAS/Envisat measurements obtained in 2011. The method not only reliably separates aerosol from ice clouds, but also provides characteristic yet overlapping correlation patterns for volcanic ash and sulfate aerosol. We demonstrate the value of the new approach for volcanic ash and sulfate aerosol originating from the Grímsvötn (Iceland, Puyehue-Cordón Caulle (Chile and Nabro (Eritrea eruptions by comparing with Atmospheric Infrared Sounder (AIRS volcanic ash and SO2 measurements.

  18. Stratospheric trace gas and aerosol profiles at McMurdo and South Pole stations

    Energy Technology Data Exchange (ETDEWEB)

    Hofmann, D.J. (Univ. of Wyoming, Laramie); Rosen, J.M.; Kjome, N.T.; Olson, G.L.; Schmeltekopf, A.L.; Goldan, P.D.; Winkler, R.H.

    1979-10-01

    During January 1979, we conducted balloon soundings in Antarctica to measure stratospheric trace gas and aerosol profiles. For the first time, we took trace gas samples at Amundsen-Scott (South Pole) Station. Four days earlier a similar experiment had been conducted at McMurdo Station. The samples, obtained by automatically opening evacuated stainless steel spheres at several altitudes, were returned to the United States and analyzed by gas chromatography at the Aeronomy Laboratory of the National Oceanic and Atmospheric Administration in Boulder, CO. The excellent agreement between McMurdo and South Pole data up to 20 kilometers suggests that trace gas concentrations in the polar regions are very uniform over a time period of at least four days and that measurements at either station are probably representative of the general antarctic profile. The same conclusion may be drawn from data on the fluorocarbons. These constituents also are very inert in the troposphere, but they undergo photodissociation in the stratosphere. As a result, their concentration drops off rapidly with altitude in the stratosphere. In addition to measuring trace gases, we again measured the stratospheric sulfate aerosol profile at McMurdo Station. Finally, we conducted a number of condensation nuclei soundings from the clean air facility at South Pole Station.

  19. Variation of the vertical distribution of Nabro volcano aerosol layers in the stratosphere observed by LIDAR

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    Noh, Young Min; Shin, Dong Ho; Müller, Detlef

    2017-04-01

    We present results of the vertical distribution variation of volcanic aerosol layers in the upper troposphere and lower stratosphere. The data were taken with our multiwavelength aerosol Raman lidar at Gwangju (35.10° N, 126.53° E), Korea. The volcanic ash particles and gases were released around 12 June 2011 during the eruption of the Nabro volcano (13.37° N, 41.7° E) in Eritrea, east Africa. Forward trajectory computations show that the volcanic aerosols were advected from North Africa to East Asia. The first measurement of the aerosol layer over Korea was on 19 June 2011. The aerosol layers appeared between 15 km and 17 km height asl (above sea level). The maximum value of the aerosol layer of the particle backscatter coefficient (1.5 ± 0.3 Mm-1 sr-1) and the linear particle depolarization ratio at 532 nm (2.2%) were observed at 16.4 km height asl. We continuously probed the upper troposphere and lower stratosphere for this volcanic aerosol layer during the following 6 months, until December 2011. The volcanic aerosol layer showed a single-peak of the particle backscatter coefficient and a comparably narrow vertical thickness at our observation site at the beginning of our observation period (i.e. comparably soon after the initial eruption period). After that initial period the vertical distribution of the plume changed. Multiple peaks and a comparably broad geometrical thickness developed with progressing observation time. The vertical thickness of the volcanic aerosol layer expanded up to 10 km by 3 August 2011. The linear particle depolarization ratios were larger in the lower part of the aerosol layer than the upper part of the aerosol layer. We observed a strong variation of the AOD (aerosol optical depth) in the first two months of our lidar observations. After these two months the AOD gradually decreased with time from September to December 20111 and the maximum particle backscatter coefficients consistently decreased. The corresponding e

  20. The impact of volcanic aerosol on the Northern Hemisphere stratospheric polar vortex: mechanisms and sensitivity to forcing structure

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    M. Toohey

    2014-06-01

    Full Text Available Observations and simple theoretical arguments suggest that the Northern Hemisphere (NH stratospheric polar vortex is stronger in winters following major volcanic eruptions. However, recent studies show that climate models forced by prescribed volcanic aerosol fields fail to reproduce this effect. We investigate the impact of volcanic aerosol forcing on stratospheric dynamics, including the strength of the NH polar vortex, in ensemble simulations with the Max Planck Institute Earth System Model. The model is forced by four different prescribed forcing sets representing the radiative properties of stratospheric aerosol following the 1991 eruption of Mt. Pinatubo: two forcing sets are based on observations, and are commonly used in climate model simulations, and two forcing sets are constructed based on coupled aerosol–climate model simulations. For all forcings, we find that temperature and zonal wind anomalies in the NH high latitudes are not directly impacted by anomalous volcanic aerosol heating. Instead, high latitude effects result from robust enhancements in stratospheric residual circulation, which in turn result, at least in part, from enhanced stratospheric wave activity. High latitude effects are therefore much less robust than would be expected if they were the direct result of aerosol heating. While there is significant ensemble variability in the high latitude response to each aerosol forcing set, the mean response is sensitive to the forcing set used. Significant differences, for example, are found in the NH polar stratosphere temperature and zonal wind response to two different forcing data sets constructed from different versions of SAGE II aerosol observations. Significant strengthening of the polar vortex, in rough agreement with the expected response, is achieved only using aerosol forcing extracted from prior coupled aerosol–climate model simulations. Differences in the dynamical response to the different forcing sets used

  1. 30-year lidar observations of the stratospheric aerosol layer state over Tomsk (Western Siberia, Russia)

    Science.gov (United States)

    Zuev, Vladimir V.; Burlakov, Vladimir D.; Nevzorov, Aleksei V.; Pravdin, Vladimir L.; Savelieva, Ekaterina S.; Gerasimov, Vladislav V.

    2017-02-01

    There are only four lidar stations in the world which have almost continuously performed observations of the stratospheric aerosol layer (SAL) state over the last 30 years. The longest time series of the SAL lidar measurements have been accumulated at the Mauna Loa Observatory (Hawaii) since 1973, the NASA Langley Research Center (Hampton, Virginia) since 1974, and Garmisch-Partenkirchen (Germany) since 1976. The fourth lidar station we present started to perform routine observations of the SAL parameters in Tomsk (56.48° N, 85.05° E, Western Siberia, Russia) in 1986. In this paper, we mainly focus on and discuss the stratospheric background period from 2000 to 2005 and the causes of the SAL perturbations over Tomsk in the 2006-2015 period. During the last decade, volcanic aerosol plumes from tropical Mt. Manam, Soufrière Hills, Rabaul, Merapi, Nabro, and Kelut and extratropical (northern) Mt. Okmok, Kasatochi, Redoubt, Sarychev Peak, Eyjafjallajökull, and Grímsvötn were detected in the stratosphere over Tomsk. When it was possible, we used the NOAA HYSPLIT trajectory model to assign aerosol layers observed over Tomsk to the corresponding volcanic eruptions. The trajectory analysis highlighted some surprising results. For example, in the cases of the Okmok, Kasatochi, and Eyjafjallajökull eruptions, the HYSPLIT air mass backward trajectories, started from altitudes of aerosol layers detected over Tomsk with a lidar, passed over these volcanoes on their eruption days at altitudes higher than the maximum plume altitudes given by the Smithsonian Institution Global Volcanism Program. An explanation of these facts is suggested. The role of both tropical and northern volcanic eruptions in volcanogenic aerosol loading of the midlatitude stratosphere is also discussed. In addition to volcanoes, we considered other possible causes of the SAL perturbations over Tomsk, i.e., the polar stratospheric cloud (PSC) events and smoke plumes from strong forest fires. At least

  2. A risk-based framework for assessing the effectiveness of stratospheric aerosol geoengineering.

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    Angus J Ferraro

    Full Text Available Geoengineering by stratospheric aerosol injection has been proposed as a policy response to warming from human emissions of greenhouse gases, but it may produce unequal regional impacts. We present a simple, intuitive risk-based framework for classifying these impacts according to whether geoengineering increases or decreases the risk of substantial climate change, with further classification by the level of existing risk from climate change from increasing carbon dioxide concentrations. This framework is applied to two climate model simulations of geoengineering counterbalancing the surface warming produced by a quadrupling of carbon dioxide concentrations, with one using a layer of sulphate aerosol in the lower stratosphere, and the other a reduction in total solar irradiance. The solar dimming model simulation shows less regional inequality of impacts compared with the aerosol geoengineering simulation. In the solar dimming simulation, 10% of the Earth's surface area, containing 10% of its population and 11% of its gross domestic product, experiences greater risk of substantial precipitation changes under geoengineering than under enhanced carbon dioxide concentrations. In the aerosol geoengineering simulation the increased risk of substantial precipitation change is experienced by 42% of Earth's surface area, containing 36% of its population and 60% of its gross domestic product.

  3. A risk-based framework for assessing the effectiveness of stratospheric aerosol geoengineering.

    Science.gov (United States)

    Ferraro, Angus J; Charlton-Perez, Andrew J; Highwood, Eleanor J

    2014-01-01

    Geoengineering by stratospheric aerosol injection has been proposed as a policy response to warming from human emissions of greenhouse gases, but it may produce unequal regional impacts. We present a simple, intuitive risk-based framework for classifying these impacts according to whether geoengineering increases or decreases the risk of substantial climate change, with further classification by the level of existing risk from climate change from increasing carbon dioxide concentrations. This framework is applied to two climate model simulations of geoengineering counterbalancing the surface warming produced by a quadrupling of carbon dioxide concentrations, with one using a layer of sulphate aerosol in the lower stratosphere, and the other a reduction in total solar irradiance. The solar dimming model simulation shows less regional inequality of impacts compared with the aerosol geoengineering simulation. In the solar dimming simulation, 10% of the Earth's surface area, containing 10% of its population and 11% of its gross domestic product, experiences greater risk of substantial precipitation changes under geoengineering than under enhanced carbon dioxide concentrations. In the aerosol geoengineering simulation the increased risk of substantial precipitation change is experienced by 42% of Earth's surface area, containing 36% of its population and 60% of its gross domestic product.

  4. A global, space-based stratospheric aerosol climatology: 1979 to 2014

    Science.gov (United States)

    Thomason, L. W.; Vernier, J. P.; Bourassa, A. E.; Millan, L.; Manney, G. L.

    2016-12-01

    Herein, we report on a global space-based stratospheric aerosol climatology (GloSSAC) that has been developed to support Coupled Model Intercomparison Project Phase 6 (CMIP6) (REF to CMIP6 and ETH work). GloSSAC is most closely related to the ASAP[SPARC, 2006] and CCMI data sets and follows a similar approach used to produce those data sets. It is primarily built using space-based measurements by a number of instruments including the SAGE series, OSIRIS, CALIPSO, CLAES and HALOE. The data set is presented as monthly depictions for 80S to 80N and from at least the tropopause to 40 km. The data set consists primarily of measurements by the instruments at their native wavelength and measurement type (e.g., extinction coefficient). However, every bin in these monthly grids receives measured or indirectly inferred values for aerosol extinction coefficient at 525 and 1020 nm. Generally, bins where no data are available are filled via simple linear interpolation in time only. The exceptions are in the SAGE I/II gap from 1982 to 1984 where data from SAM II and ground-based and airborne lidar data sets are used to span the 3 years between the end of the SAGE I mission in November 1981 and the beginning of the SAGE II mission in October 1984. Ground-based lidar also supplements space-based data in the months following the Pinatubo eruption when much of the lower stratosphere is too optically opaque for occultation measurements. This data set includes total aerosol surface area density and volume estimates based on Thomason et al.[2008] though these should be interpreted as bounding values (low and high) rather than functional aerosol parameters that are generally produced from this and predecessor data sets by other parties. Unlike previous versions of this data set, GloSSAC has been permanently archived at NASA's Atmospheric Science Data Center and a digital object identifier (doi) for GloSSAC is available. SPARC (2006), Assessment of Stratospheric Aerosol Properties (ASAP

  5. Early growth dynamical implications for the steerability of stratospheric solar radiation management via sulfur aerosol particles

    Science.gov (United States)

    Benduhn, François; Schallock, Jennifer; Lawrence, Mark G.

    2016-09-01

    Aerosol growth dynamics may have implications for the steerability of stratospheric solar radiation management via sulfur particles. This paper derives a set of critical initial growth conditions that are analyzed as a function of two key parameters: the initial concentration of the injected sulfuric acid and its dilution rate with the surrounding air. Based upon this analysis, early aerosol growth dynamical regimes may be defined and classified in terms of their likelihood to serve as candidates for the controlled generation of a radiatively effective aerosol. Our results indicate that the regime that fulfills all critical conditions would require that airplane turbines be used to provide sufficient turbulence. The regime's parameter space is narrow and related to steep gradients, thus pointing to potential fine tuning requirements. More research, development, and testing would be required to refine our findings and determine their global-scale implications.

  6. Retrieval of stratospheric aerosol size information from OSIRIS limb scattered sunlight spectra

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    A. E. Bourassa

    2008-02-01

    Full Text Available Recent work has shown that the retrieval of stratospheric aerosol vertical profiles is possible using limb scattered sunlight measurements at optical wavelengths. The aerosol number density profile is retrieved for an assumed particle size distribution and composition. This result can be used to derive the extinction at the measured wavelength. However, large systematic error can result from the uncertainty in the assumed size distribution when the result is used to estimate the extinction at other wavelengths. It is shown in this work that the addition of information obtained from the near infrared limb radiance profile at 1530 nm measured by the imaging module of the OSIRIS instrument yields an indication of the aerosol size distribution profile that can be used to improve the fidelity of the retrievals. A comparison of the estimated extinction profile at 1020 nm with coincident occultation measurements demonstrates agreement to within approximately 15% from 12 to 27 km altitude.

  7. The ISA-MIP Historical Eruption SO2 Emissions Assessment (HErSEA): an intercomparison for interactive stratospheric aerosol models

    Science.gov (United States)

    Mann, Graham; Dhomse, Sandip; Sheng, Jianxiong; Mills, Mike

    2016-04-01

    Major historical volcanic eruptions have injected huge amounts of sulphur dioxide into the stratosphere with observations showing an enhancement of the stratospheric aerosol layer for several years (ASAP, 2006). Such long-lasting increases in stratospheric aerosol loading cool the Earth's surface by scattering incoming solar radiation and warm the stratosphere via absorption of near infra-red solar and long-wave terrestrial radiation with complex effects on climate (e.g. Robock, 2000). Two recent modelling studies of Mount Pinatubo (Dhomse et al., 2014; Sheng et al. 2015) have highlighted that observations suggest the sulphur loading of the volcanically enhanced stratospheric aerosol may have been considerably lower than suggested by measurements of the injected SO2. This poster describes a new model intercomparison activity "ISA-MIP" for interactive stratospheric aerosol models within the framework of the SPARC initiative on Stratospheric Sulphur and its Role in Climate (SSiRC). The new "Historical Eruption SO2 emissions Assessment" (HErSEA) will intercompare model simulations of the three largest volcanic perturbations to the stratosphere in the last 50 years, 1963 Mt Agung, 1982 El Chichon and 1991 Mt Pinatubo. The aim is to assess how effectively the emitted SO2 translates into perturbations to stratospheric aerosol properties and simulated radiative forcings in different composition-climate models with interactive stratospheric aerosol (ISA). Each modelling group will run a mini-ensemble of transient AMIP-type runs for the 3 eruptions with a control no-eruption run followed by upper and lower bound injection amount estimates and 3 different injection height settings for two shallow (e.g. 19-21km amd 23-25km) and one deep (e.g. 19-25km) injection. First order analysis will intercompare stratospheric aerosol metrics such as 2D-monthly AOD(550nm, 1020nm) and timeseries of tropical and NH/SH mid-visible extinction at three different models levels (15, 20 and 25km

  8. Constraining the long-term climate reponse to stratospheric sulfate aerosols injection by the short-term volcanic climate response

    Science.gov (United States)

    Plazzotta, M.; Seferian, R.; Douville, H.; Kravitz, B.; Tilmes, S.; Tjiputra, J.

    2016-12-01

    Rising greenhouse gas emissions are leading to global warming and climate change, which will have multiple impacts on human society. Geoengineering methods like solar radiation management by stratospheric sulfate aerosols injection (SSA-SRM) aim at treating the symptoms of climate change by reducing the global temperature. Since a real-world testing cannot be implemented, Earth System Models (ESMs) are useful tools to assess the climate impacts of such geoengineering methods. However, coordinated simulations performed with the Geoengineering Model Intercomparison Project (GeoMIP) have shown that climate cooling in response to a continuous injection of 5Tg of SO2 per year under RCP45 future projection (the so-called G4 experiment) differs substantially between ESMs. Here, we employ a volcano analog approach to constrain the climate response in SSA-SRM geoengineering simulations across an ensemble of 10 ESMs. We identify an emergent relationship between the long-term cooling in responses to the mitigation of the clear-sky surface downwelling shortwave radiation (RSDSCS), and the short-term cooling related to the change in RSDSCS during the major tropical volcanic eruptions observed over the historical period (1850-2005). This relationship explains almost 80% of the multi-model spread. Combined with contemporary observations of the latest volcanic eruptions (satellite observations and model reanalyzes), this relationship provides a tight constraint on the climate impacts of SSA-SRM. We estimate that a continuous injection of SO2 aerosols into the stratosphere will reduce the global average temperature of continental land surface by 0.47 K per W m-2, impacting both hydrological and carbon cycles. Compared with the unconstrained ESMs ensemble (range from 0.32 to 0.92 K per W m-2 ), our estimate represents much higher confidence ways to assess the impacts of SSA-SRM on the climate while ruling the most extreme projections of the unconstrained ensemble extremely unlikely.

  9. Lidar development with applications to the stratosphere- troposphere exchange and tropical aerosol detection

    Science.gov (United States)

    Castleberg, Paul Andrew

    1997-06-01

    Lidar remote sensing of the atmosphere is explored through the use and development of the Rayleigh and resonance lidar systems at the Arecibo Observatory (18.3oN, 66.8oW). Resonance lidar capabilities have been demonstrated at the Arecibo Observatory for both sodium and potassium. The initiation, development, and details of the lidar system, based on an alexandrite solid state ring laser, are discussed. We present initial resonance observations, as well as the exciting potential for dual- wavelength upper troposphere and lower stratosphere aerosol observations. The Arecibo five year Rayleigh lidar data base and latitudinal snap shot from the Space Shuttle LITE experiment are used to study the temporal and spatial distributions of volcanic aerosols entrained in the stratosphere. The results support recent global models which suggest an extra tropical suction pump is responsible for mass being up drawn across the tropical tropopause, moved poleward, then pushed downward in the extratropics (Holton et al., 1995). The aerosol scattering wavelength dependence is introduced through the Angstrom coefficient to estimate aerosol size distributions. The analysis is extended to upper tropospheric cirrus clouds. Initial observations of two types of cirrus are presented. We speculate that one type are the remnants of convective activity, while the second grow in the cold tropical tropopause. We present a single example of the wavelength dependence as an example of the utility of multi-wavelength lidar analysis. Local stratospheric/tropospheric exchanges are investigated through a detailed discussion of lidar, radar, and balloon observations of temperatures and wind field fluctuations. On a single remarkable night, September 14-15, 1994, we captured two unique examples of convective activity at the tropopause and in the lower stratosphere. The first is a large scale molecular density depletion (temperature enhancement) just below the tropopause, which we believe is the result of

  10. Validation of aerosol measurements by the satellite sensors SAM II and Sage

    Science.gov (United States)

    Russell, P. B.; Mccormick, M. P.; Swissler, T. J.

    1982-01-01

    A global data base on stratospheric aerosols has been obtained with the aid of the sensors SAM II and SAGE since the satellites carrying the sensors were launched in October 1978 and Feburary 1979, respectively. Several major comparative experiments have been conducted to acquire correlative data for validating the extinction profiles measured by these satellite sensors. The present investigation has the objective to present results from the first two of these experiments, which were conducted at Sondrestorm, Greenland, in November 1978, and at Poker Flat, Alaska, in July 1979. In both experiments, extinction profiles derived from the correlative sensors (dustsonde, lidar, filter, wire impactor) agreed, to within their respective uncertainties, with the extinction profiles measured by SAM II and SAGE (which in turn agreed with each other).

  11. Impact of Stratospheric Volcanic Aerosols on Age-of-Air and Transport of Long-Lived Species

    Directory of Open Access Journals (Sweden)

    Giovanni Pitari

    2016-11-01

    Full Text Available The radiative perturbation associated to stratospheric aerosols from major explosive volcanic eruptions may induce significant changes in stratospheric dynamics. The aerosol heating rates warm up the lower stratosphere and cause a westerly wind anomaly, with additional tropical upwelling. Large scale transport of stratospheric trace species may be perturbed as a consequence of this intensified Brewer–Dobson circulation. The radiatively forced changes of the stratospheric circulation during the first two years after the eruption of Mt. Pinatubo (June 1991 may help explain the observed trend decline of long-lived greenhouse gases at surface stations (approximately −8 and −0.4 ppbv/year for CH4 and N2O, respectively. This decline is partly driven by the increased mid- to high-latitude downward flux at the tropopause and also by an increased isolation of the tropical pipe in the vertical layer near the tropopause, with reduced horizontal eddy mixing. Results from a climate-chemistry coupled model are shown for both long-lived trace species and the stratospheric age-of-air. The latter results to be younger by approximately 0.5 year at 30 hPa for 3–4 years after the June 1991 Pinatubo eruption, as a result of the volcanic aerosols radiative perturbation and is consistent with independent estimates based on long time series of in situ profile measurements of SF6 and CO2. Younger age of air is also calculated after Agung, El Chichón and Ruiz eruptions, as well as negative anomalies of the N2O growth rate at the extratropical tropopause layer. This type of analysis is made comparing the results of two ensembles of model simulations (1960–2005, one including stratospheric volcanic aerosols and their radiative interactions and a reference case where the volcanic aerosols do not interact with solar and planetary radiation.

  12. Geoengineering with stratospheric aerosols: What do we not know after a decade of research?

    Science.gov (United States)

    MacMartin, Douglas G.; Kravitz, Ben; Long, Jane C. S.; Rasch, Philip J.

    2016-11-01

    Any well-informed future decision on whether and how to deploy solar geoengineering requires balancing the impacts (both intended and unintended) of intervening in the climate against the impacts of not doing so. Despite tremendous progress in the last decade, the current state of knowledge remains insufficient to support an assessment of this balance, even for stratospheric aerosol geoengineering (SAG), arguably the best understood (practical) geoengineering method. We articulate key unknowns associated with SAG, including both climate-science and design questions, as an essential step toward developing a future strategic research program that could address outstanding uncertainties.

  13. Climate impact of volcanic aerosol in the stratosphere and upper troposphere - CALIPSO observations from 2006-2015

    Science.gov (United States)

    Friberg, Johan; Martinsson, Bengt G.; Andersson, Sandra M.; Sandvik, Oscar S.; Hermann, Markus; van Velthoven, Peter F. J.; Zahn, Andreas

    2017-04-01

    We have investigated the climate impact of volcanic eruptions in the period 2006-2015, and found that the volcanic perturbations of the stratospheric aerosol is stronger and lasts longer than previously thought. Recent studies (Ridley et al., 2014, Andersson et al., 2015) show that a large portion of volcanic climate impact stems from aerosol in the LMS (lowermost stratosphere). Although the LMS holds >40% of the stratospheric mass (Appenzeller et al., 1996) it is generally neglected in estimations of the stratospheric AOD (aerosol optical depth). In the past decade the stratospheric aerosol load was perturbed by a number of volcanic eruptions. We cover that period by using the CALIPSO level 1b night-time data to study the volcanic influence on the global and regional climate. CALIPSO data were averaged to a resolution of 180 m vertically and 1×1° horizontally, cleaned from ice clouds by means of the depolarization ratio (Vernier et al., 2009), and a method was developed to remove polar stratospheric clouds (PSC). This approach enables identification of aerosol also at low altitudes (currently using 4 km minimum altitude) and in the Antarctic region (60 to 90°S) where PSCs are frequent during winter. In the current study, we estimate the total stratospheric AOD and radiative forcing and find that significant fractions of volcanic aerosol were located below the static tropopause after volcanic eruptions. Volcanic aerosol was generally observed down to the dynamic tropopause, and detected down to potential vorticities of 1.5-2 PVU (almost 1 km below the static tropopause). Hence, the dynamic tropopause was found to better enclose the volcanic aerosol. Furthermore, large concentrations of aerosol from the Kasatochi eruption (Aug 2008) is found to linger in the extratropical UT (upper troposphere) for several months after the eruption. Sulphate-rich volcanic aerosol transported from the LMS may influence cirrus clouds in the extratropical UT, inducing an indirect

  14. Quantifying the temperature-independent effect of stratospheric aerosol geoengineering on global-mean precipitation in a multi-model ensemble

    Science.gov (United States)

    Ferraro, Angus J.; Griffiths, Hannah G.

    2016-03-01

    The reduction in global-mean precipitation when stratospheric aerosol geoengineering is used to counterbalance global warming from increasing carbon dioxide (CO2) concentrations has been mainly attributed to the temperature-independent effect of CO2 on atmospheric radiative cooling. We demonstrate here that stratospheric sulphate aerosol itself also acts to reduce global-mean precipitation independent of its effects on temperature. The temperature-independent effect of stratospheric aerosol geoenginering on global-mean precipitation is calculated by removing temperature-dependent effects from climate model simulations of the Geoengineering Model Intercomparison Project (GeoMIP). When sulphate aerosol is injected into the stratosphere at a rate of 5 Tg SO2 per year the aerosol reduces global-mean precipitation by approximately 0.2 %, though multiple ensemble members are required to separate this effect from internal variability. For comparison, the precipitation reduction from the temperature-independent effect of increasing CO2 concentrations under the RCP4.5 scenario of the future is approximately 0.5 %. The temperature-independent effect of stratospheric sulphate aerosol arises from the aerosol’s effect on tropospheric radiative cooling. Radiative transfer calculations show this is mainly due to increasing downward emission of infrared radiation by the aerosol, but there is also a contribution from the stratospheric warming the aerosol causes. Our results suggest climate model simulations of solar dimming can capture the main features of the global-mean precipitation response to stratospheric aerosol geoengineering.

  15. Two-Channel Satellite Retrievals of Aerosol Properties: An Overview

    Science.gov (United States)

    Mishchenko, Michael I.

    1999-01-01

    In order to reduce current uncertainties in the evaluation of the direct and indirect effects of tropospheric aerosols on climate on the global scale, it has been suggested to apply multi-channel retrieval algorithms to the full period of existing satellite data. This talk will outline the methodology of interpreting two-channel satellite radiance data over the ocean and describe a detailed analysis of the sensitivity of retrieved aerosol parameters to the assumptions made in different retrieval algorithms. We will specifically address the calibration and cloud screening issues, consider the suitability of existing satellite data sets to detecting short- and long-term regional and global changes, compare preliminary results obtained by several research groups, and discuss the prospects of creating an advanced retroactive climatology of aerosol optical thickness and size over the oceans.

  16. A decadal satellite record of gravity wave activity in the lower stratosphere to study polar stratospheric cloud formation

    Science.gov (United States)

    Hoffmann, Lars; Spang, Reinhold; Orr, Andrew; Alexander, M. Joan; Holt, Laura A.; Stein, Olaf

    2017-02-01

    Atmospheric gravity waves yield substantial small-scale temperature fluctuations that can trigger the formation of polar stratospheric clouds (PSCs). This paper introduces a new satellite record of gravity wave activity in the polar lower stratosphere to investigate this process. The record is comprised of observations of the Atmospheric Infrared Sounder (AIRS) aboard NASA's Aqua satellite from January 2003 to December 2012. Gravity wave activity is measured in terms of detrended and noise-corrected 15 µm brightness temperature variances, which are calculated from AIRS channels that are the most sensitive to temperature fluctuations at about 17-32 km of altitude. The analysis of temporal patterns in the data set revealed a strong seasonal cycle in wave activity with wintertime maxima at mid- and high latitudes. The analysis of spatial patterns indicated that orography as well as jet and storm sources are the main causes of the observed waves. Wave activity is closely correlated with 30 hPa zonal winds, which is attributed to the AIRS observational filter. We used the new data set to evaluate explicitly resolved temperature fluctuations due to gravity waves in the European Centre for Medium-Range Weather Forecasts (ECMWF) operational analysis. It was found that the analysis reproduces orographic and non-orographic wave patterns in the right places, but that wave amplitudes are typically underestimated by a factor of 2-3. Furthermore, in a first survey of joint AIRS and Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) satellite observations, nearly 50 gravity-wave-induced PSC formation events were identified. The survey shows that the new AIRS data set can help to better identify such events and more generally highlights the importance of the process for polar ozone chemistry.

  17. Total Volcanic Stratospheric Aerosol Optical Depths and Implications for Global Climate Change

    Science.gov (United States)

    Ridley, D. A.; Solomon, S.; Barnes, J. E.; Burlakov, V. D.; Deshler, T.; Dolgii, S. I.; Herber, A. B.; Nagai, T.; Neely, R. R., III; Nevzorov, A. V.; Ritter, C.; Sakai, T.; Santer, B. D.; Sato, M.; Schmidt, A.; Uchino, O.; Vernier, J. P.

    2014-01-01

    Understanding the cooling effect of recent volcanoes is of particular interest in the context of the post-2000 slowing of the rate of global warming. Satellite observations of aerosol optical depth above 15 km have demonstrated that small-magnitude volcanic eruptions substantially perturb incoming solar radiation. Here we use lidar, Aerosol Robotic Network, and balloon-borne observations to provide evidence that currently available satellite databases neglect substantial amounts of volcanic aerosol between the tropopause and 15 km at middle to high latitudes and therefore underestimate total radiative forcing resulting from the recent eruptions. Incorporating these estimates into a simple climate model, we determine the global volcanic aerosol forcing since 2000 to be 0.19 +/- 0.09W/sq m. This translates into an estimated global cooling of 0.05 to 0.12 C. We conclude that recent volcanic events are responsible for more post-2000 cooling than is implied by satellite databases that neglect volcanic aerosol effects below 15 km.

  18. Viewing Atmospheric Aerosols from the MODIS Satellite Sensor

    Science.gov (United States)

    Remer, L.

    2003-01-01

    The MODerate resolution Imaging Spectroradiometer (MODIS) currently aboard both the Terra and Aqua satellites produces a suite of products designed to characterize global aerosol distribution, optical thickness and particle size. Never before has a space-borne instrument been able to provide such detailed information, complementing field and modeling efforts to produce a comprehensive picture of aerosol characteristics. The three years of Terra-MODIS data have been validated by comparing with co-located AERONET observations of aerosol optical thickness and derivations of aerosol size parameters. Some 8000 comparison points located at 133 AERONET sites around the globe show that the MODIS aerosol optical thickness retrievals are accurate to within the pre-launch expectations, on a global basis. The global statistics, however, can hide local biases in the product. Some of these biases will be discussed. Nevertheless, the products can be used and are currently being used to answer some pressing questions concerning aerosol radiative forcing, aerosol-cloud interaction, estimating aerosol sources and height of transport, and Air Quality forecasting. A survey of current applications of MODIS aerosol products will be presented.

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

    Directory of Open Access Journals (Sweden)

    M. J. M. Penning de Vries

    2015-09-01

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

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

    Directory of Open Access Journals (Sweden)

    M. J. M. Penning de Vries

    2015-05-01

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

  1. 35 yr of stratospheric aerosol measurements at Garmisch-Partenkirchen: from Fuego to Eyjafjallajökull, and beyond

    Science.gov (United States)

    Trickl, T.; Giehl, H.; Jäger, H.; Vogelmann, H.

    2013-05-01

    Lidar measurements at Garmisch-Partenkirchen (Germany) have almost continually delivered backscatter coefficients of stratospheric aerosol since 1976. The time series is dominated by signals from the particles injected into or formed in the stratosphere due to major volcanic eruptions, in particular those of El Chichon (Mexico, 1982) and Mt Pinatubo (Philippines, 1991). Here, we focus more on the long-lasting background period since the late 1990s and 2006, in view of processes maintaining a residual lower-stratospheric aerosol layer in absence of major eruptions, as well as the period of moderate volcanic impact afterwards. During the long background period the stratospheric backscatter coefficients reached a level even below that observed in the late 1970s. This suggests that the predicted potential influence of the strongly growing air traffic on the stratospheric aerosol loading is very low. Some correlation may be found with single strong forest-fire events, but the average influence of biomass burning seems to be quite limited. No positive trend in background aerosol can be resolved over a period as long as that observed by lidar at Mauna Loa. We conclude that the increase of our integrated backscatter coefficients starting in 2008 is mostly due to volcanic eruptions with explosivity index 4, penetrating strongly into the stratosphere. Most of them occurred in the mid-latitudes. A key observation for judging the role of eruptions just reaching the tropopause region was that of the plume from the Icelandic volcano Eyjafjallajökull above Garmisch-Partenkirchen (April 2010) due to the proximity of that source. The top altitude of the ash above the volcano was reported just as 9.3 km, but the lidar measurements revealed enhanced stratospheric aerosol up to 14.3 km. Our analysis suggests for two or three of the four measurement days the presence of a stratospheric contribution from Iceland related to quasi-horizontal transport, differing from the strong descent

  2. The representation of solar cycle signals in stratospheric ozone - Part 1: A comparison of recently updated satellite observations

    Science.gov (United States)

    Maycock, Amanda C.; Matthes, Katja; Tegtmeier, Susann; Thiéblemont, Rémi; Hood, Lon

    2016-08-01

    Changes in incoming solar ultraviolet radiation over the 11-year solar cycle affect stratospheric ozone abundances. It is important to quantify the magnitude, structure, and seasonality of the associated solar-ozone response (SOR) to understand the impact of the 11-year solar cycle on climate. Part 1 of this two-part study uses multiple linear regression analysis to extract the SOR in a number of recently updated satellite ozone datasets covering different periods within the epoch 1970 to 2013. The annual mean SOR in the updated version 7.0 (v7.0) Stratospheric Aerosol and Gas Experiment (SAGE) II number density dataset (1984-2004) is very consistent with that found in the previous v6.2. In contrast, we find a substantial decrease in the magnitude of the SOR in the tropical upper stratosphere in the SAGE II v7.0 mixing ratio dataset (˜ 1 %) compared to the v6.2 (˜ 4 %). This difference is shown to be largely attributable to the change in the independent stratospheric temperature dataset used to convert SAGE II ozone number densities to mixing ratios. Since these temperature records contain substantial uncertainties, we suggest that datasets based on SAGE II number densities are currently most reliable for evaluating the SOR. We further analyse three extended ozone datasets that combine SAGE II v7.0 number densities with more recent GOMOS (Global Ozone Monitoring by Occultation of Stars) or OSIRIS (Optical Spectrograph and Infrared Imager System) measurements. The extended SAGE-OSIRIS dataset (1984-2013) shows a smaller and less statistically significant SOR across much of the tropical upper stratosphere compared to the SAGE II data alone. In contrast, the two SAGE-GOMOS datasets (1984-2011) show SORs that are in closer agreement with the original SAGE II data and therefore appear to provide a more reliable estimate of the SOR. We also analyse the SOR in the recent Solar Backscatter Ultraviolet Instrument (SBUV) Merged Ozone Dataset (SBUVMOD) version 8.6 (VN8

  3. Modeling of solar radiation management: a comparison of simulations using reduced solar constant and stratospheric sulphate aerosols

    Science.gov (United States)

    Kalidindi, Sirisha; Bala, Govindasamy; Modak, Angshuman; Caldeira, Ken

    2015-05-01

    The climatic effects of Solar Radiation Management (SRM) geoengineering have been often modeled by simply reducing the solar constant. This is most likely valid only for space sunshades and not for atmosphere and surface based SRM methods. In this study, a global climate model is used to evaluate the differences in the climate response to SRM by uniform solar constant reduction and stratospheric aerosols. Our analysis shows that when global mean warming from a doubling of CO2 is nearly cancelled by both these methods, they are similar when important surface and tropospheric climate variables are considered. However, a difference of 1 K in the global mean stratospheric (61-9.8 hPa) temperature is simulated between the two SRM methods. Further, while the global mean surface diffuse radiation increases by ~23 % and direct radiation decreases by about 9 % in the case of sulphate aerosol SRM method, both direct and diffuse radiation decrease by similar fractional amounts (~1.0 %) when solar constant is reduced. When CO2 fertilization effects from elevated CO2 concentration levels are removed, the contribution from shaded leaves to gross primary productivity (GPP) increases by 1.8 % in aerosol SRM because of increased diffuse light. However, this increase is almost offset by a 15.2 % decline in sunlit contribution due to reduced direct light. Overall both the SRM simulations show similar decrease in GPP (~8 %) and net primary productivity (~3 %). Based on our results we conclude that the climate states produced by a reduction in solar constant and addition of aerosols into the stratosphere can be considered almost similar except for two important aspects: stratospheric temperature change and the consequent implications for the dynamics and the chemistry of the stratosphere and the partitioning of direct versus diffuse radiation reaching the surface. Further, the likely dependence of global hydrological cycle response on aerosol particle size and the latitudinal and

  4. Ozone depletion in the upper stratosphere estimated from satellite and Space Shuttle data

    Science.gov (United States)

    Hilsenrath, Ernest; Cebula, Richard P.; Jackman, Charles H.

    1992-01-01

    Shuttle Solar Backscatter Ultraviolet (SSBUV) spectrometer observations of ozone concentrations in the upper stratosphere made in October 1989 are combined here with measurements made in October 1980 by the similar SBUV instruments on NASA's Nimbus-7 satellite. It is shown that the ozone concentration near 45 km has decreased during this period by about 7 +/- 2 percent. The trend is consistent with predictions of a 2D photochemical model.

  5. Retrieval of Aerosol Properties from Satellite Data

    NARCIS (Netherlands)

    Kusmierczyk-Michulec, J.; Roblez Gonzalez, C.; Decae, R.; Leeuw, G. de

    2003-01-01

    Algorithms for the retrieval of aerosol properties over land and over sea have been developed by the TNO Physics and Electronics Laboratory (TNO-FEL) for several instruments, such as AVHRR (Veefkind et al., 1998a), GOME, ATSR-2 (Veelkind et al. 1998a, b; 1999) and OMI (Torres et al. 2002). OMI will

  6. Using Satellite Aerosol Retrievals to Monitor Surface Particulate Air Quality

    Science.gov (United States)

    Levy, Robert C.; Remer, Lorraine A.; Kahn, Ralph A.; Chu, D. Allen; Mattoo, Shana; Holben, Brent N.; Schafer, Joel S.

    2011-01-01

    The MODIS and MISR aerosol products were designed nearly two decades ago for the purpose of climate applications. Since launch of Terra in 1999, these two sensors have provided global, quantitative information about column-integrated aerosol properties, including aerosol optical depth (AOD) and relative aerosol type parameters (such as Angstrom exponent). Although primarily designed for climate, the air quality (AQ) community quickly recognized that passive satellite products could be used for particulate air quality monitoring and forecasting. However, AOD and particulate matter (PM) concentrations have different units, and represent aerosol conditions in different layers of the atmosphere. Also, due to low visible contrast over brighter surface conditions, satellite-derived aerosol retrievals tend to have larger uncertainty in urban or populated regions. Nonetheless, the AQ community has made significant progress in relating column-integrated AOD at ambient relative humidity (RH) to surface PM concentrations at dried RH. Knowledge of aerosol optical and microphysical properties, ambient meteorological conditions, and especially vertical profile, are critical for physically relating AOD and PM. To make urban-scale maps of PM, we also must account for spatial variability. Since surface PM may vary on a finer spatial scale than the resolution of standard MODIS (10 km) and MISR (17km) products, we test higher-resolution versions of MODIS (3km) and MISR (1km research mode) retrievals. The recent (July 2011) DISCOVER-AQ campaign in the mid-Atlantic offers a comprehensive network of sun photometers (DRAGON) and other data that we use for validating the higher resolution satellite data. In the future, we expect that the wealth of aircraft and ground-based measurements, collected during DISCOVER-AQ, will help us quantitatively link remote sensed and ground-based measurements in the urban region.

  7. Satellite observations of aerosol and CO over Mexico City

    Science.gov (United States)

    Massie, Steven T.; Gille, John C.; Edwards, David P.; Nandi, Sreela

    The development of remote sensing satellite technology potentially will lead to the technical means to monitor air pollution emitted from large cities on a global basis. This paper presents observations by the moderate resolution imaging spectroradiometer (MODIS) and measurements of pollution in the troposphere (MOPITT) experiments of aerosol optical depths and CO mixing ratios, respectively, in the vicinity of Mexico City to illustrate current satellite capabilities. MOPITT CO mixing ratios over Mexico City, averaged between January-March 2002-2005, are 19% above regional values and the CO plume extends over 10° 2 in the free troposphere at 500 hPa. Time series of Red Automatica de Monitoreo Ambiental (RAMA) PM10, and (Aerosol Robotic Network) AERONET and MODIS aerosol optical depths, and RAMA and MOPITT CO time series are inter-compared to illustrate the different perspectives of ground based and satellite instrumentation. Finally, we demonstrate, by examining MODIS and MOPITT data in April 2003, that satellite data can be used to identify episodes in which pollution form fires influences the time series of ground based and satellite observations of urban pollution.

  8. Physical and Chemical Characterization of Particles in the Upper Troposphere and Lower Stratosphere: Microanalysis of Aerosol Impactor Samples

    Science.gov (United States)

    Sheridan, Patrick J.

    1999-01-01

    Herein is reported activities to support the characterization of the aerosol in the upper troposphere (UT) and lower stratosphere (LS) collected during the Airborne Southern Hemisphere Ozone Experiment/Measurements for Assessing the Effects of Stratospheric Aircraft (ASHOE/MAESA) missions in 1994. Through a companion proposal, another group was to measure the size distribution of aerosols in the 0.008 to 2 micrometer diameter range and to collect for us impactor samples of particles larger than about 0.02 gm. In the first year, we conducted laboratory studies related to particulate deposition patterns on our collection substrates, and have performed the analysis of many ASHOE/MAESA aerosol samples from 1994 using analytical electron microscopy (AEM). We have been building an "aerosol climatology" with these data that documents the types and relative abundances of particles observed at different latitudes and altitudes. The second year (and non-funded extension periods) saw continued analyses of impactor aerosol samples, including more ASHOE/MAESA samples, some northern hemisphere samples from the NASA Stratospheric Photochemistry Aerosols and Dynamics Expedition (SPADE) program for comparison, and a few aerosol samples from the NASA Stratospheric TRacers of Atmospheric Transport (STRAT) program. A high-resolution field emission microscope was used for the analysis and re-analysis of a number of samples to determine if this instrument was superior in performance to our conventional electron microscope. In addition, some basic laboratory studies were conducted to determine the minimum detectable and analyzable particle size for different types of aerosols. In all, 61 aerosol samples were analyzed, with a total of over 30,000 individual particle analyses. In all analyzed samples, sulfate particles comprised the major aerosol number fraction. It must be stressed that particles composed of more than one species, for example sulfate and organic carbon, were classified

  9. A model study of Fuego volcanic aerosol dispersion in the lower stratosphere

    Science.gov (United States)

    Remsberg, E. E.; Turner, R. E.; Butler, C. F.

    1982-01-01

    A zonally averaged time-dependent primitive equation model is used to simulate the dispersion of both a carbon 14 injection and the volcanic aerosol from the 1974 Fuego eruption. It is noted that both injections occurred at low latitudes to midlatitudes in the Northern Hemisphere. The eddy flux terms, which account for the major portion of the transport in the lower stratosphere of this model, are specified in a manner similar to that of Harwood and Pyle (1975). Comparisons with data underline the ability of the model to simulate the vertical character of the tracer while maintaining reasonable meridional transport times. For the aerosol study, the simulated 1/e decay time at 37 deg N and for the 16- to 21-km altitude region is 9 months, whereas lidar measurements at the same latitude give a decay time of 8 months. The simulated vertical width at half-maximum for the aerosol tracer at 37 deg N and 19 deg N and for 6 months after the event possesses values of 5.0 km and 3.6 km, respectively, whereas the observed lidar values are 4.4 km and 3.0 km, respectively. The tracer transport to the Southern Hemisphere also is in qualitative agreement with the limited data that are available.

  10. Aerosol measurements in the winter/spring Antarctic stratosphere. I - Correlative measurements with ozone. II - Impact on polar stratospheric cloud theories

    Science.gov (United States)

    Hofmann, D. J.; Rosen, J. M.; Harder, J. W.

    1988-01-01

    Aerosol measurements collected from August 25-November 3, 1986 at McMurdo Station using balloon-borne optical particle counters are examined in order to study the relationship between aerosol and ozone distribution and the formation of polar stratospheric clouds (PSCs). Ozone, aerosol, and condensation nuclei profiles, and pressure, temperature, and humidity measurements are analyzed. It is observed that the height of the stratospheric sulfate layer decreases over the period of measurement suggesting that upwelling in the votex is not important in the zone depletion process. Three theories on PSC formation are described, and the effects of the aerosol measurements on the theories are considered. The three theories are: (1) the original theory of water vapor pressure over a solution of H2SO4 of Steele et al. (1983) and Hamill and Mc Master (1984); (2) the nitric acid theory of PSCs of Toon et al. (1986) and Hamill et al. (1986); and (3) the quasi-cirrus cloud theory of Heymsfield (1986).

  11. Evaluation of Aerosol Properties in GCMs using Satellite Measurements

    Science.gov (United States)

    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.

  12. Laboratory and field studies of stratospheric aerosols: Phase changes under high supersaturation

    Science.gov (United States)

    Hallet, John

    1991-02-01

    It is well known that water in the form of isolated small droplets supercool as much as 40 C below their equilibrium melting point. Solutions similarly supercool (with respect to water) and supersaturate (with respect of the solute). Experiments are described in which bulk solutions typical of atmospheric aerosols (nitric acid, sulfuric acid, and hydrates; ammonium sulfate; ammonium bisulfate; sodium chloride) are supercooled and/or supersaturated and nucleated to initiate crystal growth. Supersaturation of 300 percent is readily attainable, with linear growth of crystals increasing roughly as (supercooling/supersaturation)sup 2. The implication of the experiments is that the situation of metastability in polar stratosphere clouds is very likely, with nucleation only occuring under a high degree of supercooling or supersaturation.

  13. Laboratory and field studies of stratospheric aerosols: Phase changes under high supersaturation

    Science.gov (United States)

    Hallet, John

    1991-01-01

    It is well known that water in the form of isolated small droplets supercool as much as 40 C below their equilibrium melting point. Solutions similarly supercool (with respect to water) and supersaturate (with respect of the solute). Experiments are described in which bulk solutions typical of atmospheric aerosols (nitric acid, sulfuric acid, and hydrates; ammonium sulfate; ammonium bisulfate; sodium chloride) are supercooled and/or supersaturated and nucleated to initiate crystal growth. Supersaturation of 300 percent is readily attainable, with linear growth of crystals increasing roughly as (supercooling/supersaturation)sup 2. The implication of the experiments is that the situation of metastability in polar stratosphere clouds is very likely, with nucleation only occuring under a high degree of supercooling or supersaturation.

  14. Precursor gases of aerosols in the Mount St. Helens eruption plumes at stratospheric altitudes

    Science.gov (United States)

    Inn, E. C. Y.; Vedder, J. F.; Condon, E. P.; Ohara, D.

    1982-01-01

    Nineteen stratospheric samples from the eruption plumes of Mount St. Helens were collected in five flight experiments. The plume samples were collected at various altitudes from 13.1 to 20.7 km by using the Ames cryogenic sampling system on board the NASA U-2 aircraft. The enriched, cryogenically collected samples were analyzed by chromatography. The concentrations of aerosols precursor gases (OCS, SO2, and CS2), CH3Cl, N2O, CF2Cl2, and CFCl3 were measured by gas chromatography. Large enhancement of the mixing ratio of SO2 and moderate enhancement of CS2 and OCS were found in the plume samples compared with similar measurement under pre-volcanic conditions. A fast decay rate of the SO2 mixing ratio in the plume was observed. Measurement of Cl(-), SO2(2-), and NO3(-) by ion chromatography was also carried out on water solutions prepared from the plume samples. The results obtained with this technique imply large mixing ratios of HCl, (NO + NO2 + HNO3), and SO2, in which these constituents are the respective sources of the anions. Measurement of the Rn222 concentration in the plume was made. Other stratospheric constituents in the plume samples, such as H2O, CO2, CH4, and CO, were also observed.

  15. Will the aerosol derived from the OCM satellite sensor be representative of the aerosol over Goa?

    Digital Repository Service at National Institute of Oceanography (India)

    Talaulikar, M.; Suresh, T.; Rodrigues, A.; Desa, E.; Chauhan, P.

    is within a tolerable limit considering the error in the instrument, measurement and satellite-derived values. Seasonal variations are also observed of the variations of the aerosol data at noon from those in the morning and evening. Variations of data...

  16. In-Situ Measurements of Changes in Stratospheric Aerosol and the N2O - Aerosol Relationship inside and outside of the Polar Vortex

    Science.gov (United States)

    Borrmann, S.; Dye, J. E.; Baumgardner, D.; Wilson, J. C.; Jonsson, H. H.; Brock, C. A.; Loewenstein, M.; Podolske, J. R.; Ferry, G. V.; Barr, K. S.

    1993-01-01

    Two optical particle counters on the ER-2, together covering a particle size diameter range from 0.1 micrometers to 23 micrometers, were used to measure the aerosol bulk quantities integral number, aerosol surface and volume, as well as detailed size distributions inside and outside of the polar vortex in the lower stratosphere. While AASE I (Arctic Airborne Stratospheric Expedition, (Dec. 1988 - Feb. 1989) was conducted in a period of relative volcanic quiescence, enhancements in aerosol number, surface and volume of factors around 10, 25 and 100 were observed during AASE II (Aug. 1991 - Mar. 1992) due to the eruption of Mt. Pinatubo. The changes in these bulk quantities as well as in the size distributions measured both outside and inside the the polar vortex are presented and compared with those obtained in polar stratospheric cloud events (AASE I). Except for a shift towards larger aerosol mixing ratios the general shape of correlograms between the measured N2O and particle mixing ratios remain similar before and after the eruption. Similar correlograms are used to interpret data from vertical profiles inside and outside of the polar vortex.

  17. Potential impact of carbonaceous aerosol on the upper troposphere and lower stratosphere (UTLS) and precipitation during Asian summer monsoon in a global model simulation

    KAUST Repository

    Fadnavis, Suvarna

    2017-09-28

    Recent satellite observations show efficient vertical transport of Asian pollutants from the surface to the upper-level anticyclone by deep monsoon convection. In this paper, we examine the transport of carbonaceous aerosols, including black carbon (BC) and organic carbon (OC), into the monsoon anticyclone using of ECHAM6-HAM, a global aerosol climate model. Further, we investigate impacts of enhanced (doubled) carbonaceous aerosol emissions on the upper troposphere and lower stratosphere (UTLS), underneath monsoon circulation and precipitation from sensitivity simulations. The model simulation shows that boundary layer aerosols are transported into the monsoon anticyclone by the strong monsoon convection from the Bay of Bengal, southern slopes of the Himalayas and the South China Sea. Doubling of emissions of both BC and OC aerosols over Southeast Asia (10° S–50° N, 65–155° E) shows that lofted aerosols produce significant warming (0.6–1 K) over the Tibetan Plateau (TP) near 400–200 hPa and instability in the middle/upper troposphere. These aerosols enhance radiative heating rates (0.02–0.03 K day−1) near the tropopause. The enhanced carbonaceous aerosols alter aerosol radiative forcing (RF) at the surface by −4.74 ± 1.42 W m−2, at the top of the atmosphere (TOA) by +0.37 ± 0.26 W m−2 and in the atmosphere by +5.11 ± 0.83 W m−2 over the TP and Indo-Gangetic Plain region (15–35° N, 80–110° E). Atmospheric warming increases vertical velocities and thereby cloud ice in the upper troposphere. Aerosol induced anomalous warming over the TP facilitates the relative strengthening of the monsoon Hadley circulation and increases moisture inflow by strengthening the cross-equatorial monsoon jet. This increases precipitation amounts over India (1–4 mm day−1) and eastern China (0.2–2 mm day−1). These results are significant at the 99 % confidence level.

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

    Science.gov (United States)

    2015-08-27

    retrievals . 15. SUBJECT TERMS ’ Aerosol, data assimilation, satellite remote sensing, visibility forecast, electro-optical propagation 16. SECURITY...innovative methods for retrieving aerosol optical depth at nighttime using Visible Infrared Imaging Radiometer Suite (VIIRS) data (Johnson et al...Orthogonal Polarization (CALIOP) aerosol and cloud layer products, as well as collocated Ozone Monitoring Instrument (OMI) Aerosol Index (Al) data and

  19. Reconciling satellite aerosol optical thickness and surface fine particle mass through aerosol liquid water

    Science.gov (United States)

    Nguyen, Thien Khoi V.; Ghate, Virendra P.; Carlton, Annmarie G.

    2016-11-01

    Summertime aerosol optical thickness (AOT) over the southeast U.S. is sharply enhanced over wintertime values. This seasonal pattern is unique and of particular interest because temperatures there have not warmed over the past 100 years. Patterns in surface fine particle mass are inconsistent with satellite reported AOT. In this work, we attempt to reconcile the spatial and temporal distribution of AOT over the U.S. with particle mass measurements at the surface by examining trends in aerosol liquid water (ALW), a particle constituent that scatters radiation and affects satellite AOT but is removed in mass measurements at routine surface monitoring sites. We employ the thermodynamic model ISORROPIAv2.1 to estimate ALW mass concentrations at Interagency Monitoring of PROtected Visual Environments sites using measured ion mass concentrations and North American Regional Reanalysis meteorological data. Excellent agreement between Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observations AOT and estimated ALW provides a plausible explanation for the discrepancies in the geographical patterns of AOT and aerosol mass measurements.

  20. Satellite Perspective of Aerosol Intercontinental Transport: From Qualitative Tracking to Quantitative Characterization

    Science.gov (United States)

    Yu, Hongbin; Remer, Lorraine A.; Kahn, Ralph A.; Chin, Mian; Zhang, Yan

    2012-01-01

    Evidence of aerosol intercontinental transport (ICT) is both widespread and compelling. Model simulations suggest that ICT could significantly affect regional air quality and climate, but the broad inter-model spread of results underscores a need of constraining model simulations with measurements. Satellites have inherent advantages over in situ measurements to characterize aerosol ICT, because of their spatial and temporal coverage. Significant progress in satellite remote sensing of aerosol properties during the Earth Observing System (EOS) era offers opportunity to increase quantitative characterization and estimates of aerosol ICT, beyond the capability of pre-EOS era satellites that could only qualitatively track aerosol plumes. EOS satellites also observe emission strengths and injection heights of some aerosols, aerosol precursors, and aerosol-related gases, which can help characterize aerosol ICT. After an overview of these advances, we review how the current generation of satellite measurements have been used to (1) characterize the evolution of aerosol plumes (e.g., both horizontal and vertical transport, and properties) on an episodic basis, (2) understand the seasonal and inter-annual variations of aerosol ICT and their control factors, (3) estimate the export and import fluxes of aerosols, and (4) evaluate and constrain model simulations. Substantial effort is needed to further explore an integrated approach using measurements from on-orbit satellites (e.g., A-Train synergy) for observational characterization and model constraint of aerosol intercontinental transport and to develop advanced sensors for future missions.

  1. Satellite perspective of aerosol intercontinental transport: From qualitative tracking to quantitative characterization

    Science.gov (United States)

    Yu, Hongbin; Remer, Lorraine A.; Kahn, Ralph A.; Chin, Mian; Zhang, Yan

    2013-04-01

    Evidence of aerosol intercontinental transport (ICT) is both widespread and compelling. Model simulations suggest that ICT could significantly affect regional air quality and climate, but the broad inter-model spread of results underscores a need of constraining model simulations with measurements. Satellites have inherent advantages over in situ measurements to characterize aerosol ICT, because of their spatial and temporal coverage. Significant progress in satellite remote sensing of aerosol properties during the Earth Observing System (EOS) era offers the opportunity to increase quantitative characterization and estimates of aerosol ICT beyond the capability of pre-EOS era satellites that could only qualitatively track aerosol plumes. EOS satellites also observe emission strengths and injection heights of some aerosols, aerosol precursors, and aerosol-related gases, which can help characterize aerosol ICT. We review how the current generation of satellite measurements have been used to (1) characterize the evolution of aerosol plumes (e.g., both horizontal and vertical transport, and properties) on an episodic basis, (2) understand the seasonal and inter-annual variations of aerosol ICT and their control factors, (3) estimate the export and import fluxes of aerosols, and (4) evaluate and constrain model simulations. Substantial effort is needed to further explore an integrated approach using measurements from on-orbit satellites (e.g., A-Train synergy) for observational characterization and model constraint of aerosol intercontinental transport and to develop advanced sensors for future missions.

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

    Science.gov (United States)

    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

  3. Coherent uncertainty analysis of aerosol measurements from multiple satellite sensors

    Directory of Open Access Journals (Sweden)

    M. Petrenko

    2013-02-01

    Full Text Available 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

  4. Coherent uncertainty analysis of aerosol measurements from multiple satellite sensors

    Directory of Open Access Journals (Sweden)

    M. Petrenko

    2013-07-01

    Full Text Available 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 7%. Squared correlation coefficient (R2 values of the satellite AOD retrievals relative to AERONET exceeded 0.8 for many of the analyzed products, while root mean square error (RMSE values for most of the AOD products were within 0.15 over land and 0.07 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 land cover types. It was observed that while MODIS, MISR, and SeaWiFS provide accurate retrievals over most of the land cover 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 closed 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 certain

  5. Certain Results of Measurements of Characteristics of Stratospheric Aerosol Layer and Total Ozone Content at Siberian Lidar Station in Tomsk

    Directory of Open Access Journals (Sweden)

    Nevzorov Aleksey

    2016-01-01

    Full Text Available We consider the results of long-term remote optical monitoring, obtained at the Siberian Lidar Station of Institute of Atmospheric Optics, Siberian Branch, Russian Academy of Sciences in Tomsk (56.5°N, 85.0°E. The scattering characteristics of stratospheric aerosol layer, obtained according to data of lidar measurements since 1986, are presented. We analyze the trends of changes in the total ozone (TO content over Tomsk for the period 1996-2013 according to data of spectrophotometric measurements with employment of Total Ozone Mapping Spectrometer (TOMS data for the period 1979-1994. We determined the periods of elevated content of stratospheric aerosol over Tomsk aftera series of explosive eruptions of volcanoes of Pacific Ring of Fire and Iceland in 2006-2011. Since the second half of 1990s, we record an increasing TO trend, equaling 0.65 DU/yr for the period 1996-2013.

  6. Background Stratospheric Aerosol Investigations Using Multi-Color Wide-Field Polarization Measurements of the Twilight Sky

    CERN Document Server

    Ugolnikov, Oleg S

    2016-01-01

    First results of multi-wavelength polarization measurements of the twilight sky background using Wide-Angle Polarization Camera (WAPC) with RGB-color CCD conducted in spring and early summer of 2016 in central Russia (55.2 deg N, 37.5 deg E) are discussed. They show the effect of aerosol scattering at altitudes up to 35 km which significantly increases to the long-wave range (620 nm, R channel). Analysis of sky color behavior during the light period of twilight with account of ozone Chappuis absorption allows to retrieve the angle dependencies of intensity and polarization of scattering on the stratospheric aerosol particles. This is used to find their effective radius, being close to 0.18-0.19 microns for stratospheric altitude range.

  7. Certain Results of Measurements of Characteristics of Stratospheric Aerosol Layer and Total Ozone Content at Siberian Lidar Station in Tomsk

    Science.gov (United States)

    Nevzorov, Aleksey; Bazhenov, Oleg; Burlakov, Vladimir; Dolgii, Sergey

    2016-06-01

    We consider the results of long-term remote optical monitoring, obtained at the Siberian Lidar Station of Institute of Atmospheric Optics, Siberian Branch, Russian Academy of Sciences in Tomsk (56.5°N, 85.0°E). The scattering characteristics of stratospheric aerosol layer, obtained according to data of lidar measurements since 1986, are presented. We analyze the trends of changes in the total ozone (TO) content over Tomsk for the period 1996-2013 according to data of spectrophotometric measurements with employment of Total Ozone Mapping Spectrometer (TOMS) data for the period 1979-1994. We determined the periods of elevated content of stratospheric aerosol over Tomsk aftera series of explosive eruptions of volcanoes of Pacific Ring of Fire and Iceland in 2006-2011. Since the second half of 1990s, we record an increasing TO trend, equaling 0.65 DU/yr for the period 1996-2013.

  8. SPICE Work Package 3: Modelling the Effects of Stratospheric Aerosol Geoengineering

    Science.gov (United States)

    Driscoll, Simon

    2015-04-01

    This talk presents the results of the SPICE Work Package 3. There is an obvious need for methods to verify the accuracy of geoengineering given no observations of a geoengineering programme. Accordingly, model ability in reproducing the observed dynamical response to volcanic eruptions is discussed using analysis of CMIP5 data and different configurations of the HadGEM2 model. With the HadGEM2-L60 model shown to be substantially better in reproducing the observed dynamical response to volcanic eruptions, simulations of GeoMIP's G4 scenario are performed. Simulated impacts of geoengineering are described, and asymmetries between the immediate onset and immediate cessation ('termination') of geoengineering are analysed. Whilst a rapid large increase in stratospheric sulphate aerosols (such as from volcanic eruptions) can cause substantial damage, most volcanic eruptions in general are not catastrophic. One may therefore suspect that an 'equal but opposite' change in radiative forcing from termination may therefore not be catastrophic, if the climatic response is simulated to be symmetric. HadGEM2 simulations reveal a substantially more rapid change in variables such as near-surface temperature and precipitation following termination than the onset, indicating that termination may be substantially more damaging and even catastrophic. Some suggestions for hemispherically asymmetric geoengineering have been proposed as a way to reduce Northern Hemisphere sea ice, for example, with lesser impacts on the rest of the climate. However, HadGEM2 simulations are performed and observations analysed following volcanic eruptions. Both indicate substantial averse consequences from hemispherically asymmetric loading of stratospheric loading on precipitation in the Sahelian region - a vulnerable region where drought has caused hundreds of thousands of deaths and created millions of refugees in the past.

  9. Glacier evolution in high-mountain Asia under stratospheric sulfate aerosol injection geoengineering

    Science.gov (United States)

    Zhao, Liyun; Yang, Yi; Cheng, Wei; Ji, Duoying; Moore, John C.

    2017-06-01

    Geoengineering by stratospheric sulfate aerosol injection may help preserve mountain glaciers by reducing summer temperatures. We examine this hypothesis for the glaciers in high-mountain Asia using a glacier mass balance model driven by climate simulations from the Geoengineering Model Intercomparison Project (GeoMIP). The G3 and G4 schemes specify use of stratospheric sulfate aerosols to reduce the radiative forcing under the Representative Concentration Pathway (RCP) 4.5 scenario for the 50 years between 2020 and 2069, and for a further 20 years after termination of geoengineering. We estimate and compare glacier volume loss for every glacier in the region using a glacier model based on surface mass balance parameterization under climate projections from three Earth system models under G3, five models under G4, and six models under RCP4.5 and RCP8.5. The ensemble projections suggest that glacier shrinkage over the period 2010-2069 is equivalent to sea-level rise of 9.0 ± 1.6 mm (G3), 9.8 ± 4.3 mm (G4), 15.5 ± 2.3 mm (RCP4.5), and 18.5 ± 1.7 mm (RCP8.5). Although G3 keeps the average temperature from increasing in the geoengineering period, G3 only slows glacier shrinkage by about 50 % relative to losses from RCP8.5. Approximately 72 % of glaciated area remains at 2069 under G3, as compared with about 30 % for RCP8.5. The widely reported reduction in mean precipitation expected for solar geoengineering is unlikely to be as important as the temperature-driven shift from solid to liquid precipitation for forcing Himalayan glacier change. The termination of geoengineering at 2069 under G3 leads to temperature rise of about 1.3 °C over the period 2070-2089 relative to the period 2050-2069 and corresponding increase in annual mean glacier volume loss rate from 0.17 to 1.1 % yr-1, which is higher than the 0.66 % yr-1 under RCP8.5 during 2070-2089.

  10. Glacier evolution in high-mountain Asia under stratospheric sulfate aerosol injection geoengineering

    Directory of Open Access Journals (Sweden)

    L. Zhao

    2017-06-01

    Full Text Available Geoengineering by stratospheric sulfate aerosol injection may help preserve mountain glaciers by reducing summer temperatures. We examine this hypothesis for the glaciers in high-mountain Asia using a glacier mass balance model driven by climate simulations from the Geoengineering Model Intercomparison Project (GeoMIP. The G3 and G4 schemes specify use of stratospheric sulfate aerosols to reduce the radiative forcing under the Representative Concentration Pathway (RCP 4.5 scenario for the 50 years between 2020 and 2069, and for a further 20 years after termination of geoengineering. We estimate and compare glacier volume loss for every glacier in the region using a glacier model based on surface mass balance parameterization under climate projections from three Earth system models under G3, five models under G4, and six models under RCP4.5 and RCP8.5. The ensemble projections suggest that glacier shrinkage over the period 2010–2069 is equivalent to sea-level rise of 9.0 ± 1.6 mm (G3, 9.8 ± 4.3 mm (G4, 15.5 ± 2.3 mm (RCP4.5, and 18.5 ± 1.7 mm (RCP8.5. Although G3 keeps the average temperature from increasing in the geoengineering period, G3 only slows glacier shrinkage by about 50 % relative to losses from RCP8.5. Approximately 72 % of glaciated area remains at 2069 under G3, as compared with about 30 % for RCP8.5. The widely reported reduction in mean precipitation expected for solar geoengineering is unlikely to be as important as the temperature-driven shift from solid to liquid precipitation for forcing Himalayan glacier change. The termination of geoengineering at 2069 under G3 leads to temperature rise of about 1.3 °C over the period 2070–2089 relative to the period 2050-2069 and corresponding increase in annual mean glacier volume loss rate from 0.17 to 1.1 % yr−1, which is higher than the 0.66 % yr−1 under RCP8.5 during 2070–2089.

  11. Data Filtering and Assimilation of Satellite Derived Aerosol Optical Depth Project

    Data.gov (United States)

    National Aeronautics and Space Administration — Satellite observations of the Earth often contain excessive noise and extensive data voids. Aerosol measurements, for instance, are obscured and contaminated by...

  12. Data Filtering and Assimilation of Satellite Derived Aerosol Optical Depth Project

    Data.gov (United States)

    National Aeronautics and Space Administration — Satellite observations of the Earth often contain excessive noise and extensive data voids. Aerosol measurements, for instance, are obscured and contaminated by...

  13. Observation of an unusual mid-stratospheric aerosol layer in the Arctic: possible sources and implications for polar vortex dynamics

    Directory of Open Access Journals (Sweden)

    M. Gerding

    Full Text Available By the beginning of winter 2000/2001, a mysterious stratospheric aerosol layer had been detected by four different Arctic lidar stations. The aerosol layer was observed first on 16 November 2000, at an altitude of about 38 km near Søndre Strømfjord, Greenland (67° N, 51° W and on 19 November 2000, near Andenes, Norway (69°  N, 16°  E. Subsequently, in early December 2000, the aerosol layer was observed near Kiruna, Sweden (68°  N, 21°  E and Ny-Ålesund, Spitsbergen (79°  N, 12°  E. No mid-latitude lidar station observed the presence of aerosols in this altitude region. The layer persisted throughout the winter 2000/2001, at least up to 12 February 2001. In November 2000, the backscatter ratio at a wavelength of 532 nm was up to 1.1, with a FWHM of about 2.5 km. By early February 2001, the layer had sedimented from an altitude of 38 km to about 26 km. Measurements at several wavelengths by the ALOMAR and Koldewey lidars indicate the particle size was between 30 and 50 nm. Depolarisation measurements reveal that the particles in the layer are aspherical, hence solid. In the mid-stratosphere, the ambient atmospheric temperature was too high to support in situ formation or existence of cloud particles consisting of ice or an acid-water solution. Furthermore, in the year 2000 there was no volcanic eruption, which could have injected aerosols into the upper stratosphere. Therefore, other origins of the aerosol, such as meteoroid debris, condensed rocket fuel, or aerosols produced under the influence of charged solar particles, will be discussed in the paper. Trajectory calculations illustrate the path of the aerosol cloud within the polar vortex and are used to link the observations at the different lidar sites. From the descent rate of  the layer and particle sedimentation rates, the mean down-ward motion of air within the polar vortex was estimated to be about 124 m/d between 35 and 30 km, with higher values at the edge of the

  14. The Influence of Stratospheric Sulphate Aerosol Deployment on the Surface Air Temperature and the Risk of an Abrupt Global Warming

    Directory of Open Access Journals (Sweden)

    Roland von Glasow

    2010-12-01

    Full Text Available We used the ‘Radiative-Convective Model of the Earth-atmosphere system’ (OGIM to investigate the cooling effects induced by sulphur injections into the stratosphere. The ensemble of numerical calculations was based on the A1B scenario from the IPCC Special Report on Emissions Scenarios (SRES. Several geoengineered scenarios were analysed, including the abrupt interruption of these injections in different scenarios and at different dates. We focused on the surface air temperature (SAT anomalies induced by stratospheric sulphate aerosol generated in order to compensate future warming. Results show that continuous deployment of sulphur into the stratosphere could induce a lasting decrease in SAT. Retaining a constant aerosol loading equivalent to 6 TgS would delay the expected global warming by 53 years. Keeping the SAT constant in a context of increasing greenhouse gases (GHGs means that the aerosol loading needs to be increased by 1.9% annually. This would offset the effect of increasing GHG under the A1B scenario. A major focus of this study was on the heating rates of SAT that would arise in different scenarios in case of an abrupt cessation of sulphur injections into the stratosphere. Our model results show that heating rates after geoengineering interruption would be 15–28 times higher than in a case without geoengineering, with likely important consequences for life on Earth. Larger initial sulphate loadings induced more intense warming rates when the geoengineering was stopped at the same time. This implies that, if sulphate loading was increased to maintain constant SAT in the light of increasing GHG concentrations, the later the geoengineering interruption was to occur, the higher the heating rates would be. Consequently, geoengineering techniques like this should only be regarded as last-resort measures and require intense further research should they ever become necessary.

  15. The Multi-Sensor Aerosol Products Sampling System (MAPSS) for Integrated Analysis of Satellite Retrieval Uncertainties

    Science.gov (United States)

    Ichoku, Charles; Petrenko, Maksym; Leptoukh, Gregory

    2010-01-01

    Among the known atmospheric constituents, aerosols represent the greatest uncertainty in climate research. Although satellite-based aerosol retrieval has practically become routine, especially during the last decade, there is often disagreement between similar aerosol parameters retrieved from different sensors, leaving users confused as to which sensors to trust for answering important science questions about the distribution, properties, and impacts of aerosols. As long as there is no consensus and the inconsistencies are not well characterized and understood ', there will be no way of developing reliable climate data records from satellite aerosol measurements. Fortunately, the most globally representative well-calibrated ground-based aerosol measurements corresponding to the satellite-retrieved products are available from the Aerosol Robotic Network (AERONET). To adequately utilize the advantages offered by this vital resource,., an online Multi-sensor Aerosol Products Sampling System (MAPSS) was recently developed. The aim of MAPSS is to facilitate detailed comparative analysis of satellite aerosol measurements from different sensors (Terra-MODIS, Aqua-MODIS, Terra-MISR, Aura-OMI, Parasol-POLDER, and Calipso-CALIOP) based on the collocation of these data products over AERONET stations. In this presentation, we will describe the strategy of the MAPSS system, its potential advantages for the aerosol community, and the preliminary results of an integrated comparative uncertainty analysis of aerosol products from multiple satellite sensors.

  16. Toward a Coherent Detailed Evaluation of Aerosol Data Products from Multiple Satellite Sensors

    Science.gov (United States)

    Ichoku, Charles; Petrenko, Maksym; Leptoukh, Gregory

    2011-01-01

    Atmospheric aerosols represent one of the greatest uncertainties in climate research. Although satellite-based aerosol retrieval has practically become routine, especially during the last decade, there is often disagreement between similar aerosol parameters retrieved from different sensors, leaving users confused as to which sensors to trust for answering important science questions about the distribution, properties, and impacts of aerosols. As long as there is no consensus and the inconsistencies are not well characterized and understood, there will be no way of developing reliable climate data records from satellite aerosol measurements. Fortunately, the most globally representative well-calibrated ground-based aerosol measurements corresponding to the satellite-retrieved products are available from the Aerosol Robotic Network (AERONET). To adequately utilize the advantages offered by this vital resource, an online Multi-sensor Aerosol Products Sampling System (MAPSS) was recently developed. The aim of MAPSS is to facilitate detailed comparative analysis of satellite aerosol measurements from different sensors (Terra-MODIS, Aqua-MODIS, TerraMISR, Aura-OMI, Parasol-POLDER, and Calipso-CALIOP) based on the collocation of these data products over AERONET stations. In this presentation, we will describe the strategy of the MASS system, its potential advantages for the aerosol community, and the preliminary results of an integrated comparative uncertainly analysis of aerosol products from multiple satellite sensors.

  17. Steady-state aerosol distributions in the extra-tropical, lower stratosphere and the processes that maintain them

    Directory of Open Access Journals (Sweden)

    J. C. Wilson

    2008-02-01

    Full Text Available Measurements of aerosol, N2O and OCS made in the Northern Hemisphere below 21 km altitude following the eruption of Pinatubo are presented and analyzed. After September 1999, the oxidation of OCS and the sedimentation of particles in the extra-tropical overworld maintain the aerosol in a steady state. This analysis empirically links precursor gas to aerosol abundance throughout this region. These processes are tracked with age-of-air which offers advantages over tracking as a function of latitude and altitude. In the extra-tropical, lowermost stratosphere, normalized volume distributions appear constant in time after the fall of 1999. Exchange with the troposphere is important in understanding aerosol evolution there. Size distributions of volcanically perturbed aerosol are included to distinguish between volcanic and non-volcanic conditions. This analysis suggests that model failures to correctly predict OCS and aerosol properties below 20 km in the Northern Hemisphere extra tropics result from inadequate descriptions of atmospheric circulation.

  18. Steady-state aerosol distributions in the extra-tropical, lower stratosphere and the processes that maintain them

    Directory of Open Access Journals (Sweden)

    J. C. Wilson

    2008-11-01

    Full Text Available Measurements of aerosol, N2O and OCS made in the Northern Hemisphere below 21 km altitude following the eruption of Pinatubo are presented and analyzed. After September 1999, the oxidation of OCS and sedimentation of particles in the extra-tropical overworld north of 45 N are found to maintain the aerosol in a steady state. This analysis empirically links precursor gas to aerosol abundance throughout this region. These processes are tracked with age-of-air which offers advantages over tracking as a function of latitude and altitude. In the extra-tropical, lowermost stratosphere, normalized volume distributions appear constant in time after the fall of 1999. Exchange with the troposphere is important in understanding aerosol evolution there. Size distributions of volcanically perturbed aerosol are included to distinguish between volcanic and non-volcanic conditions. This analysis suggests that model failures to correctly predict OCS and aerosol properties below 20 km in the Northern Hemisphere extra tropics result from inadequate descriptions of atmospheric circulation.

  19. Classification of Dust Days by Satellite Remotely Sensed Aerosol Products

    Science.gov (United States)

    Sorek-Hammer, M.; Cohen, A.; Levy, Robert C.; Ziv, B.; Broday, D. M.

    2013-01-01

    Considerable progress in satellite remote sensing (SRS) of dust particles has been seen in the last decade. From an environmental health perspective, such an event detection, after linking it to ground particulate matter (PM) concentrations, can proxy acute exposure to respirable particles of certain properties (i.e. size, composition, and toxicity). Being affected considerably by atmospheric dust, previous studies in the Eastern Mediterranean, and in Israel in particular, have focused on mechanistic and synoptic prediction, classification, and characterization of dust events. In particular, a scheme for identifying dust days (DD) in Israel based on ground PM10 (particulate matter of size smaller than 10 nm) measurements has been suggested, which has been validated by compositional analysis. This scheme requires information regarding ground PM10 levels, which is naturally limited in places with sparse ground-monitoring coverage. In such cases, SRS may be an efficient and cost-effective alternative to ground measurements. This work demonstrates a new model for identifying DD and non-DD (NDD) over Israel based on an integration of aerosol products from different satellite platforms (Moderate Resolution Imaging Spectroradiometer (MODIS) and Ozone Monitoring Instrument (OMI)). Analysis of ground-monitoring data from 2007 to 2008 in southern Israel revealed 67 DD, with more than 88 percent occurring during winter and spring. A Classification and Regression Tree (CART) model that was applied to a database containing ground monitoring (the dependent variable) and SRS aerosol product (the independent variables) records revealed an optimal set of binary variables for the identification of DD. These variables are combinations of the following primary variables: the calendar month, ground-level relative humidity (RH), the aerosol optical depth (AOD) from MODIS, and the aerosol absorbing index (AAI) from OMI. A logistic regression that uses these variables, coded as binary

  20. Investigation of trace gas to aerosol relationships over biomass burning areas using daily satellite observations

    Science.gov (United States)

    Wagner, Thomas; Penning de Vries, Marloes; Zörner, Jan; Beirle, Steffen

    2014-05-01

    The quantification and characterization of aerosols from space is a great challenge. Especially in the presence of clouds and over land surfaces, it is often difficult to distinguish the signals of aerosol scattering from scattering by cloud particles or surface reflection. Instead of deriving aerosol properties directly, satellite observations of tropospheric trace gases, emitted by the same emission sources as the aerosols, can be used to derive additional information on the aerosols. Such observations have two potential advantages: First, from the composition of trace gases, information on the aerosol type can be derived. Second, such observations are possible in the presence of clouds (although usually with reduced sensitivity if the trace gases are located below the cloud). In this feasibility study we investigate the relationship between satellite observations of trace gases (CO, NO2, HCHO, CHOCHO) and AOD (measured from satellite or ground). We also include in our comparison satellite observations of the so called UV aerosol index (UVAI), which is an indicator of the aerosol absorption. Like the trace gas observations, also the UVAI can be retrieved in the presence of clouds. We investigate aerosol-trace gas relationships over biomass burning regions. Depending on their optical properties and altitude distribution such aerosols can have a strong impact on the atmospheric energy budget through direct and indirect effects. We perform correlation analyses for selected AERONET stations and also for larger biomass burning areas by also taking into account satellite observations of fire counts.

  1. Lifting options for stratospheric aerosol geoengineering: advantages of tethered balloon systems.

    Science.gov (United States)

    Davidson, Peter; Burgoyne, Chris; Hunt, Hugh; Causier, Matt

    2012-09-13

    The Royal Society report 'Geoengineering the Climate' identified solar radiation management using albedo-enhancing aerosols injected into the stratosphere as the most affordable and effective option for geoengineering, but did not consider in any detail the options for delivery. This paper provides outline engineering analyses of the options, both for batch-delivery processes, following up on previous work for artillery shells, missiles, aircraft and free-flying balloons, as well as a more lengthy analysis of continuous-delivery systems that require a pipe connected to the ground and supported at a height of 20 km, either by a tower or by a tethered balloon. Towers are shown not to be practical, but a tethered balloon delivery system, with high-pressure pumping, appears to have much lower operating and capital costs than all other delivery options. Instead of transporting sulphuric acid mist precursors, such a system could also be used to transport slurries of high refractive index particles such as coated titanium dioxide. The use of such particles would allow useful experiments on opacity, coagulation and atmospheric chemistry at modest rates so as not to perturb regional or global climatic conditions, thus reducing scale-up risks. Criteria for particle choice are discussed, including the need to minimize or prevent ozone destruction. The paper estimates the time scales and relatively modest costs required if a tethered balloon system were to be introduced in a measured way with testing and development work proceeding over three decades, rather than in an emergency. The manufacture of a tether capable of sustaining the high tensions and internal pressures needed, as well as strong winds, is a significant challenge, as is the development of the necessary pumping and dispersion technologies. The greatest challenge may be the manufacture and launch of very large balloons, but means have been identified to significantly reduce the size of such balloons or aerostats.

  2. Satellite remote sensing of Asian aerosols: a case study of clean, polluted and dust storm days

    Directory of Open Access Journals (Sweden)

    K. H. Lee

    2010-06-01

    Full Text Available Satellite-based aerosol observation is a useful tool for the estimation of microphysical and optical characteristics of aerosol during more than three decades. Until now, a lot of satellite remote sensing techniques have been developed for aerosol detection. In East Asian region, the role of satellite observation is quite important because aerosols originating from natural and man-made pollution in this region have been recognized as an important source for regional and global scale air pollution. However, it is still difficult to retrieve aerosol over land because of the complexity of the surface reflection and complex aerosol composition, in particular, aerosol absorption. In this study, aerosol retrievals using Look-up Table (LUT based method was applied to MODerate Resolution Imaging Spectroradiometer (MODIS Level 1 (L1 calibrated reflectance data to retrieve aerosol optical thickness (AOT over East Asia. Three case studies show how the methodology works to identify those differences to obtain a better AOT retrieval. The comparison between the MODIS and Aerosol Robotic Network (AERONET shows better results when the suggested methodology using the cluster based LUTs is applied (linear slope=0.94, R=0.92 than when operational MODIS aerosol products are used (linear slope=0.78, R=0.87. In conclusion, the suggested methodology is shown to work well with aerosol models acquired by statistical clustering the observation data in East Asia.

  3. Production of satellite-derived aerosol climate data records: current status of the ESA Aerosol_cci project

    Science.gov (United States)

    de Leeuw, Gerrit; Holzer-Popp, Thomas; Pinnock, Simon

    2015-04-01

    and the Aerosol_cci team Within the ESA Climate Change Initiative (CCI) project Aerosol_cci (Phase 1: 2010 -2014; Phase 2: 2014-2017) intensive work has been conducted to improve algorithms for the retrieval of aerosol information from European sensors ATSR (3 algorithms), PARASOL, MERIS (3 algorithms), synergetic AATSR/SCIAMACHY, OMI and GOMOS. Whereas OMI and GOMOS were used to derive absorbing aerosol index and stratospheric extinction profiles, respectively, Aerosol Optical Depth (AOD) and Ångström coefficient were retrieved from the other sensors. The cooperation between the project partners, including both the retrieval teams and independent validation teams, has resulted in a strong improvement of most algorithms. In particular the AATSR retrieved AOD is qualitatively similar to that from MODIS, usually taken as the standard, MISR and SeaWiFS. This conclusion has been reached form several different ways of validation of the L2 and L3 products, using AERONET sun photometer data as the common ground-truth for the application of both 'traditional' statistical techniques and a 'scoring' technique using spatial and temporal correlations. Quantitatively, the limited AATSR swath width of 500km results in a smaller amount of data. Nevertheless, the assimilation of AATSR-retrieved AOD, together with MODIS data, contributes to improving the in the ECMWF climate model results. In addition to the multi-spectral AOD, and thus the Ångström Exponent, also a per-pixel uncertainty is provided and validated. By the end of Aerosol_cci Phase 1 the ATSR algorithms have been applied to both ATSR-2 and AATSR resulting in an AOD time series of 17 years. In phase 2 this work is continued with a focus on the further improvement of the ATSR algorithms as well as those for the other instruments and algorithms, mentioned above, which in phase 1 were considered less mature. The first efforts are on the further characterization of the uncertainties and on better understanding of the

  4. 对流层气溶胶的直接气候效应对平流层的影响%Direct Effects of Tropospheric Aerosols on Stratospheric Climate

    Institute of Scientific and Technical Information of China (English)

    宋刘明; 刘煜; 朱彬; 李维亮

    2014-01-01

    The comparison between satellite data and WACCM-3 model simulated results shows that simulated results are well consistent with satellite data in central Africa,the Arabian Peninsula,Indian subconti-nent,and most parts of China,but in south central Africa,Caribbean and Europe,the model results are lower.In short,model results can well reproduce the global distribution of aerosols,but numerical differ-ence exists in some areas. Simulation indicates that changes of stratospheric temperature are neither caused by changes of strato-spheric short-wave radiation nor decided by the changes of long-wave radiation.The changes of strato-spheric temperature are not caused by the tropospheric aerosol effect but the results of dynamic process, and the changes of longwave radiative heating rate are in response to temperature changes and mitigate the change.The process of stratospheric chemical,dynamic and radiation process are tightly coupled together. By comparison,the experiment group A including stratospheric chemical process and experiment group B not including stratospheric chemical process,it shows that the changes of temperature and wind are differ-ent in the tropospheric aerosols direct effect on stratosphere.The stratospheric chemical process is of vital importance on the tropospheric aerosols effects on stratospheric climate.Stratospheric chemical process has different effects in different seasons and in different regions,polar and high-altitude regions are consid-ered to be mostly affected,in addition,stratospheric chemical process also has great influence on the upper stratosphere.The temperature variation can reach 6 K at the most,and zonal wind variation can also reach 12 m/s.The tropospheric aerosols influence the tropospheric radiative balance,tropospheric temperature, atmospheric circulation and EP flux,and changes in EP flux indicate the planetary wave propagation chan-ges. Planetary wave propagation changes make the stratospheric climate change:Stratospheric

  5. A comparison of lidar and balloon-borne particle counter measurements of the stratospheric aerosol 1974-1980

    Science.gov (United States)

    Swissler, T. J.; Hamill, P.; Osborn, M.; Russell, P. B.; McCormick, M. P.

    1982-04-01

    The optical radar measurements considered in the present investigation are those which have been obtained routinely at Hampton, VA (37.1 deg N, 76.3 deg W) since 1974. The dustsonde measurements are those made monthly at Laramie, WY (41.2 deg N, 105 deg W). The extensive data sets acquired with these two instruments during the time period 1974-80 permit a long-term comparison of the two different measurement techniques. The balloon-borne dustsonde pumps ambient air in a well-defined stream through an illuminated chamber where individual aerosol particles scatter light into photodetectors. The optical radar system used in the studies has a ruby laser with a 48-inch Cassegrainian configured telescope mounted on a mobile platform to collect the backscattered laser light. The investigation shows that optical radar measurements, dustsonde measurements, and realistic optical models together give a very consistent picture of stratospheric aerosol behavior.

  6. Deriving atmospheric visibility from satellite retrieved aerosol optical depth

    Science.gov (United States)

    Riffler, M.; Schneider, Ch.; Popp, Ch.; Wunderle, S.

    2009-04-01

    Atmospheric visibility is a measure that reflects different physical and chemical properties of the atmosphere. In general, poor visibility conditions come along with risks for transportation (e.g. road traffic, aviation) and can negatively impact human health since visibility impairment often implies the presence of atmospheric pollution. Ambient pollutants, particulate matter, and few gaseous species decrease the perceptibility of distant objects. Common estimations of this parameter are usually based on human observations or devices that measure the transmittance of light from an artificial light source over a short distance. Such measurements are mainly performed at airports and some meteorological stations. A major disadvantage of these observations is the gap between the measurements, leaving large areas without any information. As aerosols are one of the most important factors influencing atmospheric visibility in the visible range, the knowledge of their spatial distribution can be used to infer visibility with the so called Koschmieder equation, which relates visibility and atmospheric extinction. In this study, we evaluate the applicability of satellite aerosol optical depth (AOD) products from the Advanced Very High Resolution Radiometer (AVHRR) and Moderate Resolution Imaging Spectroradiometer (MODIS) to infer atmospheric visibility on large spatial scale. First results applying AOD values scaled with the planetary boundary layer height are promising. For the comparison we use a full automated and objective procedure for the estimation of atmospheric visibility with the help of a digital panorama camera serving as ground truth. To further investigate the relation between the vertical measure of AOD and the horizontal visibility data from the Aerosol Robotic Network (AERONET) site Laegeren (Switzerland), where the digital camera is mounted, are included as well. Finally, the derived visibility maps are compared with synoptical observations in central

  7. Probing into the aging dynamics of biomass burning aerosol by using satellite measurements of aerosol optical depth and carbon monoxide

    Science.gov (United States)

    Konovalov, Igor B.; Beekmann, Matthias; Berezin, Evgeny V.; Formenti, Paola; Andreae, Meinrat O.

    2017-04-01

    Carbonaceous aerosol released into the atmosphere from open biomass burning (BB) is known to undergo considerable chemical and physical transformations (aging). However, there is substantial controversy about the nature and observable effects of these transformations. A shortage of consistent observational evidence on BB aerosol aging processes under different environmental conditions and at various temporal scales hinders development of their adequate representations in chemistry transport models (CTMs). In this study, we obtain insights into the BB aerosol dynamics by using available satellite measurements of aerosol optical depth (AOD) and carbon monoxide (CO). The basic concept of our method is to consider AOD as a function of the BB aerosol photochemical age (that is, the time period characterizing the exposure of BB aerosol emissions to atmospheric oxidation reactions) predicted by means of model tracers. We evaluate the AOD enhancement ratio (ER) defined as the ratio of optical depth of actual BB aerosol with respect to that of a modeled aerosol tracer that is assumed to originate from the same fires as the real BB aerosol but that is not affected by any aging processes. To limit possible effects of model transport errors, the AOD measurements are normalized to CO column amounts that are also retrieved from satellite measurements. The method is applied to the analysis of the meso- and synoptic-scale evolution of aerosol in smoke plumes from major wildfires that occurred in Siberia in summer 2012. AOD and CO retrievals from MODIS and IASI measurements, respectively, are used in combination with simulations performed with the CHIMERE CTM. The analysis indicates that aging processes strongly affected the evolution of BB aerosol in the situation considered, especially in dense plumes (with spatial average PM2. 5 concentration exceeding 100 µg m-3). For such plumes, the ER is found to increase almost 2-fold on the scale of ˜ 10 h of daytime aerosol evolution

  8. Observing upper troposphere-lower stratosphere climate with radio occultation data from the CHAMP satellite

    Energy Technology Data Exchange (ETDEWEB)

    Foelsche, Ulrich; Borsche, Michael; Steiner, Andrea K.; Gobiet, Andreas; Pirscher, Barbara; Kirchengast, Gottfried [University of Graz, Wegener Center for Climate and Global Change (WegCenter) and Institute for Geophysics, Astrophysics, and Meteorology (IGAM), Graz (Austria); Wickert, Jens; Schmidt, Torsten [GeoForschungsZentrum Potsdam (GFZ), Potsdam (Germany)

    2008-07-15

    climatologies is estimated to be <0.5 K below 30 km. The recently launched Taiwan/U.S. FORMOSAT-3/COSMIC constellation of 6 RO satellites started to provide thousands of RO profiles per day, but already now the single-satellite CHAMP RO climatologies improve upon modern operational climatologies in the upper troposphere-lower stratosphere and can act as absolute reference climatologies for validation of more bias-sensitive climate datasets and models. (orig.)

  9. Temperature response of the troposphere and stratosphere to changes in gas and aerosol composition of the atmosphere

    Science.gov (United States)

    Dyominov, I. G.; Zadorozhny, A. M.; Elansky, N. F.

    2003-04-01

    A numerical 2-D zonally averaged interactive model of the troposphere and stratosphere including aerosol physics is used for investigation of temperature changes caused by discharges to the atmosphere of sulphate species during the Pinatubo eruption and by anthropogenic pollution of the atmosphere by CO_2, CH_4, N_2O, CFCs, HCFCs, HFCs, CH_3CCl_3 and CCl_4. The model calculates self-consistently diabatic circulation, temperature, distributions of 45 minor gas constituents, and condensed particles of sulphuric acid hydrate with radii 6.4 nm discharges of sulphate species to the atmosphere during the Pinatubo eruption led to significant changes of sulfate aerosol layer, ozone, and temperature regime of the troposphere and stratosphere. For example, we have in tropics (20oS-20oN) a temperature increase of bout 2.5-3.5 K at altitudes of 22-24 km and decrease of about 0.8-1.0 K at altitudes of 5-8 km. Discharges of sulphate species from the Pinatubo eruption significantly increased also the aerosol optical thickness of the stratosphere, which led to an about 0.3 K decrease in monthly mean global temperature at the Earth's surface by the end of 1992. The calculations of the long-term temperature variations due to anthropogenic emission show that the greatest temperature changes are observed in the Southern Hemisphere in winter/spring periods. For example, the temperature changes at a height of 40 km at 45oS in December 2050 are about -4.85 K, 0.89 K, -2.21 K, and -4.32 K respectively for anthropogenic discharges of CO_2, CH_4, N_2O, and chlorine species. The changes in the Northern Hemisphere are smaller. They are equal to about -4.5 K, 0.68 K, -1.46 K, and -3.17 K at 45oN. The temperature changes in the stratosphere are caused by the corresponding ozone variations and temperature feedbacks. In the troposphere, the temperature changes are determined by the greenhouse effect caused by optically active pollutants. For example, temperature increases near the Earth's surface

  10. Implication of future large-scale stratospheric aerosol injection on the land and ocean biogeochemistry

    Science.gov (United States)

    Tjiputra, Jerry; Grini, Alf

    2015-04-01

    In this study, we address several outstanding and emerging issues of future climate geoengineering, particularly its impact on the global biogeochemical. Applying a state-of-the-art fully interactive Earth system model, we simulate two cases of artificial stratospheric aerosol injection (SAI) on top of future RCP8.5 scenario. In the first case, the SAI brings the projection of global mean surface temperature down to the RCP4.5 level by the end of this century. For the same climate target, the non-mitigated, climate engineered scenario leads to approximately 100% and 50% more carbon sinks by the ocean and terrestrial biosphere, respectively. Consequently, the reduction in ocean surface pH is approximately three times stronger than the mitigated RCP4.5 scenario. In the second SAI case, stronger climate engineering (CE) could bring the projected temperature at 2100 down to the 2000 level. In this case, warming still occurs in the Arctic regions. Compared to the reference RCP8.5 without CE, the net global cumulative carbon uptake by land and ocean only increase slightly. Regionally, the biggest difference in carbon inventory were simulated in the mid-latitude northern hemisphere over land and the North Atlantic and Southern Oceans. Over land, reduced soil respiration overcomes reduction in the net primary production associated primarily with the cooler climate. In the North Atlantic, stabilized meridional overturning allows for more carbon sequestered into the ocean interior, while the absence of poleward amplification of Southern Annual Mode leads to less outgassing of natural carbon in the Southern Ocean. CE-induced cooling also alleviates the reduction of net primary production in the equatorial Pacific related to stratification change. Following SAI termination in 2100, rapid warming in the next few years was simulated, bringing the global temperature up to the reference RCP8.5 simulation level. By 2200, the net cumulative carbon sinks by land and ocean is

  11. Monitoring and tracking the trans-Pacific transport of aerosols using multi-satellite aerosol optical depth retrievals

    Directory of Open Access Journals (Sweden)

    A. R. Naeger

    2015-10-01

    Full Text Available The primary goal of this study was to generate a near-real time (NRT aerosol optical depth (AOD product capable of providing a comprehensive understanding of the aerosol spatial distribution over the Pacific Ocean in order to better monitor and track the trans-Pacific transport of aerosols. Therefore, we developed a NRT product that takes advantage of observations from both low-earth orbiting and geostationary satellites. In particular, we utilize AOD products from the Moderate Resolution Imaging Spectroradiometer (MODIS and Suomi National Polar-orbiting Partnership (NPP Visible Infrared Imaging Radiometer Suite (VIIRS satellites. Then, we combine these AOD products with our own retrieval algorithms developed for the NOAA Geostationary Operational Environmental Satellite (GOES-15 and Japan Meteorological Agency (JMA Multi-functional Transport Satellite (MTSAT-2 to generate a NRT daily AOD composite product. We present examples of the daily AOD composite product for a case study of trans-Pacific transport of Asian pollution and dust aerosols in mid-March 2014. Overall, the new product successfully tracks this aerosol plume during its trans-Pacific transport to the west coast of North America. However, we identify several areas across the domain of interest from Asia to North America where the new product can encounter significant uncertainties due to the inclusion of the geostationary AOD retrievals. The uncertainties associated with geostationary AOD retrievals are expected to be minimized after the successful launch of the next-generation advanced NOAA GOES-R and recently launched JMA Himawari satellites. Observations from these advanced satellites will ultimately provide an enhanced understanding of the spatial and temporal distribution of aerosols over the Pacific.

  12. Remote sensing assessment of absorbing aerosol over Peninsular Malaysia from OMI onboard Aura satellite

    Science.gov (United States)

    Tan, K. C.; Lim, H. S.; Mat Jafri, M. Z.

    2017-05-01

    The observation of aerosol index derived from the Ozone Monitoring Instrument (OMI) on board the Dutch-Finnish Aura satellite with spatial resolution 1° x 1° have been analyzed over Peninsular Malaysia for 2013-2015, from June to September, respectively. The results show significant spatial and temporal variabilities in aerosol index with higher values during June 2013 and September 2015. On the other hand, the aerosol index does not show significant differences between the Peninsular Malaysia for the remaining study duration. The high positive aerosol index values over Southern Peninsular Malaysia clearly reveal the ultraviolet absorbing nature of smoke particles affecting the area during Indonesia forest fire, associated with the Southwest monsoon season. The spatial distribution of aerosol index has been analyzed using monthly OMI/Aura data obtained from the NASA-operated Giovanni. The result shows that the satellite measurements can measure and observe the increase of the aerosol index over different regions.

  13. Satellite observations of cloud regime development: the role of aerosol processes

    OpenAIRE

    E. Gryspeerdt; Stier, P.; D. G. Partridge

    2013-01-01

    Many different interactions between aerosols and clouds have been postulated based on correlations between satellite retrieved aerosol and cloud properties. Previous studies highlighted the importance of meteorological covariability to the observed correlations. In this work, we make use of multiple temporally-spaced satellite retrievals to observe the development of cloud regimes. The observation of cloud regime development allows us to account for the influences of cloud fraction (C...

  14. Satellite observations of cloud regime development: the role of aerosol processes

    OpenAIRE

    E. Gryspeerdt; Stier, P.; D. G. Partridge

    2014-01-01

    Many different interactions between aerosols and clouds have been postulated, based on correlations between satellite retrieved aerosol and cloud properties. Previous studies highlighted the importance of meteorological covariations to the observed correlations. In this work, we make use of multiple temporally-spaced satellite retrievals to observe the development of cloud regimes. The observation of cloud regime development allows us to account for the influences of clo...

  15. Comparison of stratospheric temperature profiles from a ground-based microwave radiometer with lidar, radiosonde and satellite data

    Science.gov (United States)

    Navas-Guzmán, Francisco; Kämpfer, Niklaus; Haefele, Alexander; Keckhut, Philippe; Hauchecorne, Alain

    2015-04-01

    The importance of the knowledge of the temperature structure in the atmosphere has been widely recognized. Temperature is a key parameter for dynamical, chemical and radiative processes in the atmosphere. The cooling of the stratosphere is an indicator for climate change as it provides evidence of natural and anthropogenic climate forcing just like surface warming ( [1] and references therein). However, our understanding of the observed stratospheric temperature trend and our ability to test simulations of the stratospheric response to emissions of greenhouse gases and ozone depleting substances remains limited. Stratospheric long-term datasets are sparse and obtained trends differ from one another [1]. Therefore it is important that in the future such datasets are generated. Different techniques allow to measure stratospheric temperature profiles as radiosonde, lidar or satellite. The main advantage of microwave radiometers against these other instruments is a high temporal resolution with a reasonable good spatial resolution. Moreover, the measurement at a fixed location allows to observe local atmospheric dynamics over a long time period, which is crucial for climate research. TEMPERA (TEMPERature RAdiometer) is a newly developed ground-based microwave radiometer designed, built and operated at the University of Bern. The instrument and the retrieval of temperature profiles has been described in detail in [2]. TEMPERA is measuring a pressure broadened oxygen line at 53.1 GHz in order to determine stratospheric temperature profiles. The retrieved profiles of TEMPERA cover an altitude range of approximately 20 to 45 km with a vertical resolution in the order of 15 km. The lower limit is given by the instrumental baseline and the bandwidth of the measured spectrum. The upper limit is given by the fact that above 50 km the oxygen lines are splitted by the Zeeman effect in the terrestrial magnetic field. In this study we present a comparison of stratospheric

  16. Retrieving the Height of Smoke and Dust Aerosols by Synergistic Use of Multiple Satellite Sensors

    Science.gov (United States)

    Lee, Jaehwa; Hsu, N. Christina; Bettenhausen, Corey; Sayer, Andrew M.; Seftor, Colin J.; Jeong, Myeong-Jae

    2016-01-01

    The Aerosol Single scattering albedo and Height Estimation (ASHE) algorithm was first introduced in Jeong and Hsu (2008) to provide aerosol layer height and single scattering albedo (SSA) for biomass burning smoke aerosols. By using multiple satellite sensors synergistically, ASHE can provide the height information over much broader areas than lidar observations alone. The complete ASHE algorithm uses aerosol data from MODIS or VIIRS, OMI or OMPS, and CALIOP. A simplified algorithm also exists that does not require CALIOP data as long as the SSA of the aerosol layer is provided by another source. Several updates have recently been made: inclusion of dust layers in the retrieval process, better determination of the input aerosol layer height from CALIOP, improvement in aerosol optical depth (AOD) for nonspherical dust, development of quality assurance (QA) procedure, etc.

  17. Combined Use of Polar and Geostationary Satellite Sensors For Aerosol Characterization Over The Ocean

    Science.gov (United States)

    Costa, M. J.; Cervino, M.; Levizzani, V.; Silva, A. M.

    Aerosol particles play an important role in the Earth's climate due to their direct and indirect interaction with the atmosphere. Monitoring of the optical properties of atmospheric aerosol is thus crucial for a radiative forcing quantification at the lo- cal, regional and global scales. Ground-based measurements provide accurate aerosol properties. However, given the strong spatial and temporal variability of tropospheric aerosols ground measurements cannot cover the global scale. On the other hand, satellite-based algorithms for aerosol retrievals presently do not match the accuracy of ground-based results. Most satellite algorithms are based on a single sensor, thus often suffering from specific limitations (poor spatial or spectral resolution, long re- visitation time, poor cloud mask). A method to exploit the synergy between the polar orbiting Global Ozone Monitoring Experiment (GOME) onboard ERS-2 and the METEOSAT geostationary system was proposed (Costa et al., 2001), aiming at increasing the accuracy of the aerosol charac- terization and monitoring of the optical thickness. A validation of the algorithm is done by comparing satellite retrievals with results obtained via independent space-time co- located ground-based measurements from AERONET (Aerosol Robotic NETwork) and from other state of the art algorithms that make use of satellite measurements such as the MODIS official aerosol product. Results of the ongoing validation are pre- sented for relevant transport events of desert dust and biomass burning aerosol over the Atlantic and Indian Oceans during year 2000. References: Costa,M.J., M.Cervino, E.Cattani, F.Torricella, V.Levizzani, and A.M.Silva, 2001: "Aerosol characterization and optical thickness retrievals using GOME and METEOSAT satellite data". Meteor. Atmos. Phys., (in press). Acknowledgements: METEOSAT imagery was kindly made available by EUMET- SAT. We thank the AERONET investigators and their staff for establishing and main- taining the

  18. Characterization of absorbing aerosol types using ground and satellites based observations over an urban environment

    Science.gov (United States)

    Bibi, Samina; Alam, Khan; Chishtie, Farrukh; Bibi, Humera

    2017-02-01

    In this paper, for the first time, an effort has been made to seasonally characterize the absorbing aerosols into different types using ground and satellite based observations. For this purpose, optical properties of aerosol retrieved from AErosol RObotic NETwork (AERONET) and Ozone Monitoring Instrument (OMI) were utilized over Karachi for the period 2012 to 2014. Firstly, OMI AODabs was validated with AERONET AODabs and found to have a high degree of correlation. Then, based on this validation, characterization was conducted by analyzing aerosol Fine Mode Fraction (FMF), Angstrom Exponent (AE), Absorption Angstrom Exponent (AAE), Single Scattering Albedo (SSA) and Aerosol Index (AI) and their mutual correlation, to identify the absorbing aerosol types and also to examine the variability in seasonal distribution. The absorbing aerosols were characterized into Mostly Black Carbon (BC), Mostly Dust and Mixed BC & Dust. The results revealed that Mostly BC aerosols contributed dominantly during winter and postmonsoon whereas, Mostly Dust were dominant during summer and premonsoon. These types of absorbing aerosol were also confirmed with MODerate resolution Imaging Spectroradiometer (MODIS) and Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observation (CALIPSO) observations.

  19. Intercomparison and evaluation of satellite peroxyacetyl nitrate observations in the upper troposphere-lower stratosphere

    Science.gov (United States)

    Pope, Richard J.; Richards, Nigel A. D.; Chipperfield, Martyn P.; Moore, David P.; Monks, Sarah A.; Arnold, Stephen R.; Glatthor, Norbert; Kiefer, Michael; Breider, Tom J.; Harrison, Jeremy J.; Remedios, John J.; Warneke, Carsten; Roberts, James M.; Diskin, Glenn S.; Huey, Lewis G.; Wisthaler, Armin; Apel, Eric C.; Bernath, Peter F.; Feng, Wuhu

    2016-11-01

    Peroxyacetyl nitrate (PAN) is an important chemical species in the troposphere as it aids the long-range transport of NOx and subsequent formation of O3 in relatively clean remote regions. Over the past few decades observations from aircraft campaigns and surface sites have been used to better understand the regional distribution of PAN. However, recent measurements made by satellites allow for a global assessment of PAN in the upper troposphere-lower stratosphere (UTLS). In this study, we investigate global PAN distributions from two independent retrieval methodologies, based on measurements from the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) instrument, on board Envisat from the Institute of Meteorology and Climate Research (IMK), Karlsruhe Institute of Technology, and the Department of Physics and Astronomy, University of Leicester (UoL). Retrieving PAN from MIPAS is challenging due to the weak signal in the measurements and contamination from other species. Therefore, we compare the two MIPAS datasets with observations from the Atmospheric Chemistry Experiment Fourier transform spectrometer (ACE-FTS), in situ aircraft data and the 3-D chemical transport model TOMCAT. MIPAS shows peak UTLS PAN concentrations over the biomass burning regions (e.g. ranging from 150 to > 200 pptv at 150 hPa) and during the summertime Asian monsoon as enhanced convection aids the vertical transport of PAN from the lower atmosphere. At 150 hPa, we find significant differences between the two MIPAS datasets in the tropics, where IMK PAN concentrations are larger by 50-100 pptv. Comparisons between MIPAS and ACE-FTS show better agreement with the UoL MIPAS PAN concentrations at 200 hPa, but with mixed results above this altitude. TOMCAT generally captures the magnitude and structure of climatological aircraft PAN profiles within the observational variability allowing it to be used to investigate the MIPAS PAN differences. TOMCAT-MIPAS comparisons show that the

  20. Aerosol indirect effects -- general circulation model intercomparison and evaluation with satellite data

    Energy Technology Data Exchange (ETDEWEB)

    Quaas, Johannes; Ming, Yi; Menon, Surabi; Takemura, Toshihiko; Wang, Minghuai; Penner, Joyce E.; Gettelman, Andrew; Lohmann, Ulrike; Bellouin, Nicolas; Boucher, Olivier; Sayer, Andrew M.; Thomas, Gareth E.; McComiskey, Allison; Feingold, Graham; Hoose, Corinna; Kristjansson, Jon Egill; Liu, Xiaohong; Balkanski, Yves; Donner, Leo J.; Ginoux, Paul A.; Stier, Philip; Feichter, Johann; Sednev, Igor; Bauer, Susanne E.; Koch, Dorothy; Grainger, Roy G.; Kirkevag, Alf; Iversen, Trond; Seland, Oyvind; Easter, Richard; Ghan, Steven J.; Rasch, Philip J.; Morrison, Hugh; Lamarque, Jean-Francois; Iacono, Michael J.; Kinne, Stefan; Schulz, Michael

    2009-04-10

    Aerosol indirect effects continue to constitute one of the most important uncertainties for anthropogenic climate perturbations. Within the international AEROCOM initiative, the representation of aerosol-cloud-radiation interactions in ten different general circulation models (GCMs) is evaluated using three satellite datasets. The focus is on stratiform liquid water clouds since most GCMs do not include ice nucleation effects, and none of the model explicitly parameterizes aerosol effects on convective clouds. We compute statistical relationships between aerosol optical depth (Ta) and various cloud and radiation quantities in a manner that is consistent between the models and the satellite data. It is found that the model-simulated influence of aerosols on cloud droplet number concentration (Nd) compares relatively well to the satellite data at least over the ocean. The relationship between Ta and liquid water path is simulated much too strongly by the models. It is shown that this is partly related to the representation of the second aerosol indirect effect in terms of autoconversion. A positive relationship between total cloud fraction (fcld) and Ta as found in the satellite data is simulated by the majority of the models, albeit less strongly than that in the satellite data in most of them. In a discussion of the hypotheses proposed in the literature to explain the satellite-derived strong fcld - Ta relationship, our results indicate that none can be identified as unique explanation. Relationships similar to the ones found in satellite data between Ta and cloud top temperature or outgoing long-wave radiation (OLR) are simulated by only a few GCMs. The GCMs that simulate a negative OLR - Ta relationship show a strong positive correlation between Ta and fcld The short-wave total aerosol radiative forcing as simulated by the GCMs is strongly influenced by the simulated anthropogenic fraction of Ta, and parameterisation assumptions such as a lower bound on Nd

  1. Effect of volcanic aerosol on stratospheric NO2 and N2O5 from 2002–2014 as measured by Odin-OSIRIS and Envisat-MIPAS

    Directory of Open Access Journals (Sweden)

    C. Adams

    2017-07-01

    Full Text Available Following the large volcanic eruptions of Pinatubo in 1991 and El Chichón in 1982, decreases in stratospheric NO2 associated with enhanced aerosol were observed. The Optical Spectrograph and Infrared Imaging Spectrometer (OSIRIS measured the widespread enhancements of stratospheric aerosol following seven volcanic eruptions between 2002 and 2014, although the magnitudes of these eruptions were all much smaller than the Pinatubo and El Chichón eruptions. In order to isolate and quantify the relationship between volcanic aerosol and NO2, NO2 anomalies were calculated using measurements from OSIRIS and the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS. In the tropics, variability due to the quasi-biennial oscillation was subtracted from the time series. OSIRIS profile measurements indicate that the strongest anticorrelations between NO2 and volcanic aerosol extinction were for the 5 km layer starting  ∼  3 km above the climatological mean tropopause at the given latitude. OSIRIS stratospheric NO2 partial columns in this layer were found to be smaller than background NO2 levels during these aerosol enhancements by up to  ∼  60 % with typical Pearson correlation coefficients of R ∼ −0. 7. MIPAS also observed decreases in NO2 partial columns during periods affected by volcanic aerosol, with percent differences of up to  ∼  25 % relative to background levels. An even stronger anticorrelation was observed between OSIRIS aerosol optical depth and MIPAS N2O5 partial columns, with R ∼ −0. 9, although no link with MIPAS HNO3 was observed. The variation in OSIRIS NO2 with increasing aerosol was found to be consistent with simulations from a photochemical box model within the estimated model uncertainty.

  2. 4-D comparison method to study the NOy partitioning in summer polar stratosphere – Influence of aerosol burden

    Directory of Open Access Journals (Sweden)

    G. Dufour

    2005-01-01

    Full Text Available On 21–22 August 2001, NO, NO2 and HNO3 mixing ratio profiles were measured at high latitudes during sunset and sunrise using the Limb Profile Monitor of the Atmosphere (LPMA and the DOAS experiments under stratospheric balloon. Photochemical simulations using the chemistry module of the Reprobus Chemistry Transport Model (CTM that are constrained by ozone and total NOy balloon observations reproduce well the partitioning of NOx and NOy when model results are calculated at the exact time and location of the measurement for each tangent altitude. Taking the recently recommended reaction rate coefficients for the NOy partitioning (JPL-2003 and using realistic aerosol surface area in order to initialise the model leads to an agreement between calculations and measurements better than 10% all over the covered altitude range.

  3. Near-global aerosol mapping in the upper troposphere and lowermost stratosphere with data from the CARIBIC project

    Energy Technology Data Exchange (ETDEWEB)

    Heintzenberg, Jost; Hermann, Markus; Weigelt, Andreas (Leibniz Inst. for Tropospheric Research, Leipzig (Germany)), e-mail: jost@tropos.de; Clarke, Antony; Kapustin, Vladimir (Univ. of Hawaii, Dept. of Oceanography, Honolulu (United States)); Anderson, Bruce; Thornhill, Kenneth (NASA Langley Research Center, Hampton (United States)); Velthoven, Peter van (Royal Netherlands Meteorological Inst. (KNMI) (Netherlands)); Zahn, Andreas (Inst. for Meteorology and Climate Research, Karlsruhe Inst. of Technology (KIT), Karlsruhe (Germany)); Brenninkmeijer, Carl (Max Planck Inst. for Chemistry, Atmospheric Chemistry Div., Mainz (Germany))

    2011-11-15

    This study extrapolates aerosol data of the CARIBIC project from 1997 until June 2008 in along trajectories to compose large-scale maps and vertical profiles of submicrometre particle concentrations in the upper troposphere and lowermost stratosphere (UT/LMS). The extrapolation was validated by comparing extrapolated values with CARIBIC data measured near the respective trajectory position and by comparing extrapolated CARIBIC data to measurements by other experiments near the respective trajectory positions. Best agreement between extrapolated and measured data is achieved with particle lifetimes longer than the maximum length of used trajectories. The derived maps reveal regions of strong and frequent new particle formation, namely the Tropical Central and Western Africa with the adjacent Atlantic, South America, the Caribbean and Southeast Asia. These regions of particle formation coincide with those of frequent deep convective clouds. Vertical particle concentration profiles for the troposphere and the stratosphere confirm statistically previous results indicating frequent new particle formation in the tropopause region. There was no statistically significant increase in Aitken mode particle concentration between the first period of CARIBIC operation, 1997-2002, and the second period, 2004-2009. However, a significant increase in concentration occurred within the latter period when considering it in isolation

  4. A stratospheric aerosol increase during 1981, observed by lidar over mid-Europe

    Science.gov (United States)

    Reiter, R.; Jaeger, H.; Carnuth, W.; Funk, W.

    1982-04-01

    Lidar observations of variations in the aerosol layer due to the eruptions of Mt. St. Helens and the volcano Alaid in the Kurile Islands are reported and compared. One year after the Mt. St. Helens activity the backscattering coefficient had reduced to within 10% of the values observed in the pre-eruption period. Observed peaks were found to be moving upward, eventually forming a broad aerosol layer at 15-17 km height in July, 1981. The Alaid plume moved west to east and was determined to be the cause of aerosol disturbances up to the 20 km level. Data is presented of the time variation of the aerosol quantities and the time variation of the space resolved integral backscattering. Additional data has shown that both the Mt. St. Helens and the Alaid eruptions caused only one-third the aerosol perturbations as the Fuego eruption of 1974.

  5. Monitoring and tracking the trans-Pacific transport of aerosols using multi-satellite aerosol optical depth composites

    Science.gov (United States)

    Naeger, Aaron R.; Gupta, Pawan; Zavodsky, Bradley T.; McGrath, Kevin M.

    2016-06-01

    The primary goal of this study was to generate a near-real time (NRT) aerosol optical depth (AOD) product capable of providing a comprehensive understanding of the aerosol spatial distribution over the Pacific Ocean, in order to better monitor and track the trans-Pacific transport of aerosols. Therefore, we developed a NRT product that takes advantage of observations from both low-earth orbiting and geostationary satellites. In particular, we utilize AOD products from the Moderate Resolution Imaging Spectroradiometer (MODIS) and Suomi National Polar-orbiting Partnership (NPP) Visible Infrared Imaging Radiometer Suite (VIIRS) satellites. Then, we combine these AOD products with our own retrieval algorithms developed for the NOAA Geostationary Operational Environmental Satellite (GOES-15) and Japan Meteorological Agency (JMA) Multi-functional Transport Satellite (MTSAT-2) to generate a NRT daily AOD composite product. We present examples of the daily AOD composite product for a case study of trans-Pacific transport of Asian pollution and dust aerosols in mid-March 2014. Overall, the new product successfully tracks this aerosol plume during its trans-Pacific transport to the west coast of North America as the frequent geostationary observations lead to a greater coverage of cloud-free AOD retrievals equatorward of about 35° N, while the polar-orbiting satellites provide a greater coverage of AOD poleward of 35° N. However, we note several areas across the domain of interest from Asia to North America where the GOES-15 and MTSAT-2 retrieval algorithms can introduce significant uncertainties into the new product.

  6. Spatial Distribution of Accuracy of Aerosol Retrievals from Multiple Satellite Sensors

    Science.gov (United States)

    Petrenko, Maksym; Ichoku, Charles

    2012-01-01

    Remote sensing of aerosols from space has been a subject of extensive research, with multiple sensors retrieving aerosol properties globally on a daily or weekly basis. The diverse algorithms used for these retrievals operate on different types of reflected signals based on different assumptions about the underlying physical phenomena. Depending on the actual retrieval conditions and especially on the geographical location of the sensed aerosol parcels, the combination of these factors might be advantageous for one or more of the sensors and unfavorable for others, resulting in disagreements between similar aerosol parameters retrieved from different sensors. In this presentation, we will demonstrate the use of the Multi-sensor Aerosol Products Sampling System (MAPSS) to analyze and intercompare aerosol retrievals from multiple spaceborne sensors, including MODIS (on Terra and Aqua), MISR, OMI, POLDER, CALIOP, and SeaWiFS. Based on this intercomparison, we are determining geographical locations where these products provide the greatest accuracy of the retrievals and identifying the products that are the most suitable for retrieval at these locations. The analyses are performed by comparing quality-screened satellite aerosol products to available collocated ground-based aerosol observations from the Aerosol Robotic Network (AERONET) stations, during the period of 2006-2010 when all the satellite sensors were operating concurrently. Furthermore, we will discuss results of a statistical approach that is applied to the collocated data to detect and remove potential data outliers that can bias the results of the analysis.

  7. Urban aerosol properties, their radiative effects and the verification of different satellite retrievals of urban aerosol pollution

    Science.gov (United States)

    Chubarova, Nataly; Sviridenkov, Mikhail; Kopeikin, Vladimir; Emilenko, Alexander; Verichev, Konstantin; Skorokhod, Andrei; Semutnikova, Evgenia

    2013-04-01

    The effects of urban pollution on different aerosol properties and their year-to-year-changes in various atmospheric conditions were studied according to long-term simultaneous measurements by the collocated AERONET CIMEL sun/sky photometers in Moscow (large megacity) and at Zvenigorod (nearby clean area) for 2006-2012 year period. Additional measurements of PM10 and PM2.5, as well as soot content observations were used for evaluating the effects of local urban sources and their influence on columnar aerosol properties (single scattering albedo, aerosol optical thickness, etc.) and, hence, on radiative properties of aerosol. We discuss the results of the comparisons between RT modeling and high quality ground-based radiative measurements, which provide validation of the obtained urban radiative effects for different aerosols in clear-sky conditions. Special attention was paid to testing the retrievals of several aerosol parameters (AOT, single scattering albedo, Angstrom exponent, etc) over the urban area and the detection of the urban aerosol pollution by different satellite instruments (MISR, MODIS, SEAWIFS, OMI) against the data of collocated AERONET CIMEL sun/sky photometers in different atmospheric conditions over snow and snow-free surfaces.

  8. A climatology of fine absorbing biomass burning, urban and industrial aerosols detected from satellites

    Science.gov (United States)

    Kalaitzi, Nikoleta; Hatzianastassiou, Nikos; Gkikas, Antonis; Papadimas, Christos D.; Torres, Omar; Mihalopoulos, Nikos

    2017-04-01

    Natural biomass burning (BB) along with anthropogenic urban and industrial aerosol particles, altogether labeled here as BU aerosols, contain black and brown carbon which both absorb strongly the solar radiation. Thus, BU aerosols warm significantly the atmosphere also causing adjustments to cloud properties, which traditionally are known as cloud indirect and semi-direct effects. Given the role of the effects of BU aerosols for contemporary and future climate change, and the uncertainty associated with BU, both ascertained by the latest IPCC reports, there is an urgent need for improving our knowledge on the spatial and temporal variability of BU aerosols all over the globe. Over the last few decades, thanks to the rapid development of satellite observational techniques and retrieval algorithms it is now possible to detect BU aerosols based on satellite measurements. However, care must be taken in order to ensure the ability to distinguish BU from other aerosol types usually co-existing in the Earth's atmosphere. In the present study, an algorithm is presented, based on a synergy of different satellite measurements, aiming to identify and quantify BU aerosols over the entire globe and during multiple years. The objective is to build a satellite-based climatology of BU aerosols intended for use for various purposes. The produced regime, namely the spatial and temporal variability of BU aerosols, emphasizes the BU frequency of occurrence and their intensity, in terms of aerosol optical depth (AOD). The algorithm is using the following aerosol optical properties describing the size and atmospheric loading of BU aerosols: (i) spectral AOD, (ii) Ångström Exponent (AE), (iii) Fine Fraction (FF) and (iv) Aerosol Index (AI). The relevant data are taken from Collection 006 MODIS-Aqua, except for AI which is taken from OMI-Aura. The identification of BU aerosols by the algorithm is based on a specific thresholding technique, with AI≥1.5, AE≥1.2 and FF≥0.6 threshold

  9. Intercomparison of daytime stratospheric NO2 satellite retrievals and model simulations

    NARCIS (Netherlands)

    Belmonte Rivas, M.; Veefkind, J.P.; Boersma, F.; Levelt, P.; Eskes, H.; Gille, J.

    2014-01-01

    This paper evaluates the agreement between stratospheric NO2 retrievals from infrared limb sounders (Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) and High Resolution Dynamics Limb Sounder (HIRDLS)) and solar UV/VIS backscatter sensors (Ozone Monitoring Instrument (OMI), Scanning

  10. The impact of stratospheric volcanic aerosol on decadal-scale climate predictions

    Science.gov (United States)

    Timmreck, Claudia; Pohlmann, Holger; Illing, Sebastian; Kadow, Christopher

    2016-04-01

    The possibility of a large future volcanic eruption provides arguably the largest uncertainty concerning the evolution of the climate system on the time scale of a few years; but also the greatest opportunity to learn about the behavior of the climate system, and our models thereof. So the question emerges how large will the uncertainty be for future decadal climate predictions if no volcanic aerosol is taken into account? And how strong has volcanic aerosol affected decadal prediction skill on annual and multi-year seasonal scales over the CMIP5 hindcast period? To understand the impact of volcanic aerosol on multi-year seasonal and decadal climate predictions we performed CMIP5-type hindcasts without volcanic aerosol using the German MiKlip prediction system system baseline 1 from 1961 to 1991 and compared them to the corresponding simulations including aerosols. Our results show that volcanic aerosol significantly affects the prediction skill for global mean surface air temperature in the first five years after strong volcanic eruptions. Also on the regional scale a volcanic imprint on decadal-scale variability is detectable. Neglecting volcanic aerosol leads to a reduced prediction skill over the tropical and subtropical Atlantic, Indic and West Pacific but to an improvement over the tropical East-Pacific, where the model has in general no skill. Multi-seasonal differences in the skill for seasonal-mean temperatures are evident over Continental Europe with significant skill loss due to neglection of volcanic aerosol in boreal winter over central Europe, Scandinavia and over south-eastern Europe and the East-Mediterranean in boreal summer.

  11. Chemical Composition and Dynamics of the Upper Troposphere and the Lower Stratosphere: Overview of the Project

    Science.gov (United States)

    Sofieva, V. F.; Liu, C.; Huang, F.; Kyrola, E.; Liu, Y.; Ialongo, I.; Hakkarainen, J.; Zhang, Y.

    2016-08-01

    The DRAGON-3 cooperation study on the upper troposphere and the lower stratosphere (UTLS) is based on new satellite data and modern atmospheric models. The objectives of the project are: (i) assessment of satellite data on chemical composition in UTLS, (ii) dynamical and chemical structures of the UTLS and its variability, (iii) multi-scale variability of stratospheric ozone, (iv) climatology of the stratospheric aerosol layer and its variability, and (v) updated ozone climatology and its relation to tropopause/multiple tropopauses.In this paper, we present the main results of the project.

  12. Satellite observations and modeling of transport in the upper troposphere through the lower mesosphere during the 2006 major stratospheric sudden warming

    Directory of Open Access Journals (Sweden)

    W. H. Daffer

    2009-07-01

    Full Text Available An unusually strong and prolonged stratospheric sudden warming (SSW in January 2006 was the first major SSW for which globally distributed long-lived trace gas data are available covering the upper troposphere through the lower mesosphere. We use Aura Microwave Limb Sounder (MLS, Atmospheric Chemistry Experiment-Fourier Transform Spectrometer (ACE-FTS data, the SLIMCAT Chemistry Transport Model (CTM, and assimilated meteorological analyses to provide a comprehensive picture of transport during this event. The upper tropospheric ridge that triggered the SSW was associated with an elevated tropopause and layering in trace gas profiles in conjunction with stratospheric and tropospheric intrusions. Anomalous poleward transport (with corresponding quasi-isentropic troposphere-to-stratosphere exchange at the lowest levels studied in the region over the ridge extended well into the lower stratosphere. In the middle and upper stratosphere, the breakdown of the polar vortex transport barrier was seen in a signature of rapid, widespread mixing in trace gases, including CO, H2O, CH4 and N2O. The vortex broke down slightly later and more slowly in the lower than in the middle stratosphere. In the middle and lower stratosphere, small remnants with trace gas values characteristic of the pre-SSW vortex lingered through the weak and slow recovery of the vortex. The upper stratospheric vortex quickly reformed, and, as enhanced diabatic descent set in, CO descended into this strong vortex, echoing the fall vortex development. Trace gas evolution in the SLIMCAT CTM agrees well with that in the satellite trace gas data from the upper troposphere through the middle stratosphere. In the upper stratosphere and lower mesosphere, the SLIMCAT simulation does not capture the strong descent of mesospheric CO and H2O values into the reformed vortex; this poor CTM performance in the upper stratosphere and lower mesosphere results

  13. A sensitivity analysis of Ring effect to aerosol properties and comparison to satellite observations

    Directory of Open Access Journals (Sweden)

    T. Wagner

    2010-12-01

    Full Text Available In this study we explore the sensitivity of satellite observations of the Ring effect (at various wavelengths to atmospheric aerosol properties. Compared to clouds, aerosols have a rather weak influence on the Ring effect, thus the requirements on the accuracy of the measurements and the radiative transfer simulations are high. In this study, we show that for moderate and high aerosol optical depth (AOD, Ring effect observations are sensitive enough to yield information not only on the AOD, but also on the absorbing properties of aerosols and the aerosol layer height. The latter two quantities are especially important for the determination of the radiative effects of aerosols.

    Our investigations are based on observations by the satellite instrument SCIAMACHY on ENVISAT (2004–2008 and on model simulations using the Monte-Carlo radiative transfer model McArtim. In addition to the Ring effect we investigate the impact of aerosols on the absorptions of the oxygen molecule (O2 and dimer (O4 as well as the radiance. In general good consistency between measured and simulated quantities is found. In some cases also systematic differences occurred, which are probably mainly related to the strong polarisation sensitivity of the SCIAMACHY instrument.

    Our study indicates that Ring effect observations have important advantages for aerosol retrievals: they can be analysed with high accuracy in various wavelength ranges; and depending on the wavelength range, they show different sensitivities on aerosol properties like single scattering albedo, optical depth or layer height. The results of this study are of particular interest for future aerosol inversion algorithms for satellite instruments with reduced polarisation sensitivity and smaller ground pixels, capable of measuring the Ring effect with higher accuracy.

  14. Evaluation of a size-resolved aerosol model based on satellite and ground observations and its implication on aerosol forcing

    Science.gov (United States)

    Ma, Xiaoyan; Yu, Fangqun

    2016-04-01

    The latest AeroCom phase II experiments have showed a large diversity in the simulations of aerosol concentrations, size distribution, vertical profile, and optical properties among 16 detailed global aerosol microphysics models, which contribute to the large uncertainty in the predicted aerosol radiative forcing and possibly induce the distinct climate change in the future. In the last few years, we have developed and improved a global size-resolved aerosol model (Yu and Luo, 2009; Ma et al., 2012; Yu et al., 2012), GEOS-Chem-APM, which is a prognostic multi-type, multi-component, size-resolved aerosol microphysics model, including state-of-the-art nucleation schemes and condensation of low volatile secondary organic compounds from successive oxidation aging. The model is one of 16 global models for AeroCom phase II and participated in a couple of model inter-comparison experiments. In this study, we employed multi-year aerosol optical depth (AOD) data from 2004 to 2012 taken from ground-based Aerosol Robotic Network (AERONET) measurements and Moderate Resolution Imaging Spectroradiometer (MODIS), Multiangle Imaging SpectroRadiometer (MISR) and Sea-viewing Wide Field-of-view Sensor (SeaWiFS) satellite retrievals to evaluate the performance of the GEOS-Chem-APM in predicting aerosol optical depth, including spatial distribution, reginal variation and seasonal variabilities. Compared to the observations, the modelled AOD is overall good over land, but quite low over ocean possibly due to low sea salt emission in the model and/or higher AOD in satellite retrievals, specifically MODIS and MISR. We chose 72 AERONET sites having at least 36 months data available and representative of high spatial domain to compare with the model and satellite data. Comparisons in various representative regions show that the model overall agrees well in the major anthropogenic emission regions, such as Europe, East Asia and North America. Relative to the observations, the modelled AOD is

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

    Science.gov (United States)

    2015-08-27

    indicate that the assimilation of satellite observations significantly improves NAAPS aerosol forecasting capability and reliability. To fully utilize...method derives a semi-quantitative indicator of nighttime x using artificial light sources. Nighttime x retrievals from the newly-developed method are...Kemper, T. Craig, I. Ginis , Evaluation of Maine aerosol production simulated using the WaveWatchlll prognostic Wave Model coupled to the Community

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

    Science.gov (United States)

    Bonine, Lauren

    2015-01-01

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

  17. Direct Radiative Forcing of Anthropogenic Aerosols over Oceans from Satellite Observations

    Institute of Scientific and Technical Information of China (English)

    CHEN Lin; SHI Guangyu; QIN Shiguang; YANG Su; ZHANG Peng

    2011-01-01

    Anthropogenic aerosols play an important role in the atmospheric energy balance. Anthropogenic aerosol optical depth (AOD) and its accompanying shortwave radiative forcing (RF) are usually simulated by numerical models. Recently, with the development of space-borne instruments and sophisticated retrieval algorithms, it has become possible to estimate aerosol radiative forcing based on satellite observations. In this study, we have estimated shortwave direct radiative forcing due to anthropogenic aerosols over oceans in all-sky conditions by combining clouds and the Single Scanner Footprint data of the Clouds and Earth's Radiant Energy System (CERES/SSF) experiment, which provide measurements of upward shortwave fluxes at the top of atmosphere, with Moderate Resolution Imaging Spectroradiometer (MODIS) aerosol and cloud products. We found that globally averaged aerosol radiative forcing over oceans in the clear-sky conditions and all-sky conditions were -1.03±0.48 W m-2 and -0.34 ±0.16 W m-2, respectively. Direct radiative forcing by anthropogenic aerosols shows large regional and seasonal variations. In some regions and in particular seasons, the magnitude of direct forcing by anthropogenic aerosols can be comparable to the forcing of greenhouse gases. However, it shows that aerosols caused the cooling effect, rather than warming effect from global scale, which is different from greenhouse gases.

  18. Maritime Aerosol Network as a Component of AERONET - First Results and Comparison with Global Aerosol Models and Satellite Retrievals

    Science.gov (United States)

    Smirnov, A.; Holben, B. N.; Giles, D. M.; Slutsker, I.; O'Neill, N. T.; Eck, T. F.; Macke, A.; Croot, P.; Courcoux, Y.; Sakerin, S. M.; Smyth, T. J.; Zielinski, T.; Zibordi, G.; Goes, J. I.; Harvey, M. J.; Quinn, P. K.; Nelson, N. B.; Radionov, V. F.; Duarte, C. M.; Remer, L. A.; Kahn, R. A.; Kleidman, R. G.; Gaitley, B. J.; Tan, Q.; Diehl, T. L.

    2011-01-01

    The Maritime Aerosol Network (MAN) has been collecting data over the oceans since November 2006. Over 80 cruises were completed through early 2010 with deployments continuing. Measurement areas included various parts of the Atlantic Ocean, the Northern and Southern Pacific Ocean, the South Indian Ocean, the Southern Ocean, the Arctic Ocean and inland seas. MAN deploys Microtops handheld sunphotometers and utilizes a calibration procedure and data processing traceable to AERONET. Data collection included areas that previously had no aerosol optical depth (AOD) coverage at all, particularly vast areas of the Southern Ocean. The MAN data archive provides a valuable resource for aerosol studies in maritime environments. In the current paper we present results of AOD measurements over the oceans, and make a comparison with satellite AOD retrievals and model simulations.

  19. Spatio-temporal distribution of localized aerosol loading in China: A satellite view

    Science.gov (United States)

    Sun, Kun; Chen, Xiaoling

    2017-08-01

    In recent years, haze pollution and high concentrations of particulate matter frequently occur in many mega cities of China, which has seriously impacted the regional air quality, and further caused harm to human health. Although satellite observation provides a convenient way to evaluate air quality in space and time, satellite measurements do not separate between natural and anthropogenic aerosols. To discriminate anthropogenic aerosol contribution from satellite observations, we proposed the concept of Local Aerosol Optical Depth (LAOD) to describe the localized aerosol loading. A comparative analysis was performed between seasonal/monthly Mean AOD (MAOD), LAOD and ground measured PM2.5/PM10. The comparison results show that LAOD has better linear relationship with PM2.5/PM10 than MAOD in central and eastern China with persistent localized aerosol emissions. Based on the MODIS Deep Blue AOD dataset from 2001 to 2015, we analyzed the spatio-temporal distribution of LAOD over China. Spatially, high LAODs are mainly distributed in Sichuan basin, North China Plain, and central China; temporally, LAOD over China presents an upward trend (+0.003 year-1) during 2001-2007 and a weak downward (-0.002 year-1) trend from 2008 to 2015. LAOD was also found to be highly correlated with haze frequency over most areas of central and eastern China, especially in North China Plain with a correlation coefficient of 0.87 (P aerosol emission on regional haze pollution in China.

  20. Comparisons of aerosol backscatter using satellite and ground lidars: implications for calibrating and validating spaceborne lidar

    Science.gov (United States)

    Gimmestad, Gary; Forrister, Haviland; Grigas, Tomas; O’Dowd, Colin

    2017-01-01

    The Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP) instrument on the polar orbiter Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observation (CALIPSO) is an elastic backscatter lidar that produces a global uniformly-calibrated aerosol data set. Several Calibration/Validation (Cal/Val) studies for CALIOP conducted with ground-based lidars and CALIOP data showed large aerosol profile disagreements, both random and systematic. In an attempt to better understand these problems, we undertook a series of ground-based lidar measurements in Atlanta, Georgia, which did not provide better agreement with CALIOP data than the earlier efforts, but rather prompted us to investigate the statistical limitations of such comparisons. Meaningful Cal/Val requires intercomparison data sets with small enough uncertainties to provide a check on the maximum expected calibration error. For CALIOP total attenuated backscatter, reducing the noise to the required level requires averaging profiles along the ground track for distances of at least 1,500 km. Representative comparison profiles often cannot be acquired with ground-based lidars because spatial aerosol inhomogeneities introduce systematic error into the averages. These conclusions have implications for future satellite lidar Cal/Val efforts, because planned satellite lidars measuring aerosol backscatter, wind vector, and CO2 concentration profiles may all produce data requiring considerable along-track averaging for meaningful Cal/Val. PMID:28198389

  1. Comparisons of aerosol backscatter using satellite and ground lidars: implications for calibrating and validating spaceborne lidar

    Science.gov (United States)

    Gimmestad, Gary; Forrister, Haviland; Grigas, Tomas; O’Dowd, Colin

    2017-02-01

    The Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP) instrument on the polar orbiter Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observation (CALIPSO) is an elastic backscatter lidar that produces a global uniformly-calibrated aerosol data set. Several Calibration/Validation (Cal/Val) studies for CALIOP conducted with ground-based lidars and CALIOP data showed large aerosol profile disagreements, both random and systematic. In an attempt to better understand these problems, we undertook a series of ground-based lidar measurements in Atlanta, Georgia, which did not provide better agreement with CALIOP data than the earlier efforts, but rather prompted us to investigate the statistical limitations of such comparisons. Meaningful Cal/Val requires intercomparison data sets with small enough uncertainties to provide a check on the maximum expected calibration error. For CALIOP total attenuated backscatter, reducing the noise to the required level requires averaging profiles along the ground track for distances of at least 1,500 km. Representative comparison profiles often cannot be acquired with ground-based lidars because spatial aerosol inhomogeneities introduce systematic error into the averages. These conclusions have implications for future satellite lidar Cal/Val efforts, because planned satellite lidars measuring aerosol backscatter, wind vector, and CO2 concentration profiles may all produce data requiring considerable along-track averaging for meaningful Cal/Val.

  2. Direct Radiative Effect of Aerosols Based on PARASOL and OMI Satellite Observations

    Science.gov (United States)

    Lacagnina, Carlo; Hasekamp, Otto P.; Torres, Omar

    2017-01-01

    Accurate portrayal of the aerosol characteristics is crucial to determine aerosol contribution to the Earth's radiation budget. We employ novel satellite retrievals to make a new measurement-based estimate of the shortwave direct radiative effect of aerosols (DREA), both over land and ocean. Global satellite measurements of aerosol optical depth, single-scattering albedo (SSA), and phase function from PARASOL (Polarization and Anisotropy of Reflectances for Atmospheric Sciences coupled with Observations from a Lidar) are used in synergy with OMI (Ozone Monitoring Instrument) SSA. Aerosol information is combined with land-surface bidirectional reflectance distribution function and cloud characteristics from MODIS (Moderate Resolution Imaging Spectroradiometer) satellite products. Eventual gaps in observations are filled with the state-of-the-art global aerosol model ECHAM5-HAM2. It is found that our estimate of DREA is largely insensitive to model choice. Radiative transfer calculations show that DREA at top-of-atmosphere is -4.6 +/- 1.5 W/sq m for cloud-free and -2.1 +/- 0.7 W/sq m for all-sky conditions, during year 2006. These fluxes are consistent with, albeit generally less negative over ocean than, former assessments. Unlike previous studies, our estimate is constrained by retrievals of global coverage SSA, which may justify different DREA values. Remarkable consistency is found in comparison with DREA based on CERES (Clouds and the Earth's Radiant Energy System) and MODIS observations.

  3. Comparisons of aerosol backscatter using satellite and ground lidars: implications for calibrating and validating spaceborne lidar.

    Science.gov (United States)

    Gimmestad, Gary; Forrister, Haviland; Grigas, Tomas; O'Dowd, Colin

    2017-02-15

    The Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP) instrument on the polar orbiter Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observation (CALIPSO) is an elastic backscatter lidar that produces a global uniformly-calibrated aerosol data set. Several Calibration/Validation (Cal/Val) studies for CALIOP conducted with ground-based lidars and CALIOP data showed large aerosol profile disagreements, both random and systematic. In an attempt to better understand these problems, we undertook a series of ground-based lidar measurements in Atlanta, Georgia, which did not provide better agreement with CALIOP data than the earlier efforts, but rather prompted us to investigate the statistical limitations of such comparisons. Meaningful Cal/Val requires intercomparison data sets with small enough uncertainties to provide a check on the maximum expected calibration error. For CALIOP total attenuated backscatter, reducing the noise to the required level requires averaging profiles along the ground track for distances of at least 1,500 km. Representative comparison profiles often cannot be acquired with ground-based lidars because spatial aerosol inhomogeneities introduce systematic error into the averages. These conclusions have implications for future satellite lidar Cal/Val efforts, because planned satellite lidars measuring aerosol backscatter, wind vector, and CO2 concentration profiles may all produce data requiring considerable along-track averaging for meaningful Cal/Val.

  4. Direct radiative effect of aerosols based on PARASOL and OMI satellite observations

    Science.gov (United States)

    Lacagnina, Carlo; Hasekamp, Otto P.; Torres, Omar

    2017-02-01

    Accurate portrayal of the aerosol characteristics is crucial to determine aerosol contribution to the Earth's radiation budget. We employ novel satellite retrievals to make a new measurement-based estimate of the shortwave direct radiative effect of aerosols (DREA), both over land and ocean. Global satellite measurements of aerosol optical depth, single-scattering albedo (SSA), and phase function from PARASOL (Polarization and Anisotropy of Reflectances for Atmospheric Sciences coupled with Observations from a Lidar) are used in synergy with OMI (Ozone Monitoring Instrument) SSA. Aerosol information is combined with land-surface bidirectional reflectance distribution function and cloud characteristics from MODIS (Moderate Resolution Imaging Spectroradiometer) satellite products. Eventual gaps in observations are filled with the state-of-the-art global aerosol model ECHAM5-HAM2. It is found that our estimate of DREA is largely insensitive to model choice. Radiative transfer calculations show that DREA at top-of-atmosphere is -4.6 ± 1.5 W/m2 for cloud-free and -2.1 ± 0.7 W/m2 for all-sky conditions, during year 2006. These fluxes are consistent with, albeit generally less negative over ocean than, former assessments. Unlike previous studies, our estimate is constrained by retrievals of global coverage SSA, which may justify different DREA values. Remarkable consistency is found in comparison with DREA based on CERES (Clouds and the Earth's Radiant Energy System) and MODIS observations.

  5. Direct Radiative Effect of Aerosols Based on PARASOL and OMI Satellite Observations

    Science.gov (United States)

    Lacagnina, Carlo; Hasekamp, Otto P.; Torres, Omar

    2017-01-01

    Accurate portrayal of the aerosol characteristics is crucial to determine aerosol contribution to the Earth's radiation budget. We employ novel satellite retrievals to make a new measurement-based estimate of the shortwave direct radiative effect of aerosols (DREA), both over land and ocean. Global satellite measurements of aerosol optical depth, single-scattering albedo (SSA), and phase function from PARASOL (Polarization and Anisotropy of Reflectances for Atmospheric Sciences coupled with Observations from a Lidar) are used in synergy with OMI (Ozone Monitoring Instrument) SSA. Aerosol information is combined with land-surface bidirectional reflectance distribution function and cloud characteristics from MODIS (Moderate Resolution Imaging Spectroradiometer) satellite products. Eventual gaps in observations are filled with the state-of-the-art global aerosol model ECHAM5-HAM2. It is found that our estimate of DREA is largely insensitive to model choice. Radiative transfer calculations show that DREA at top-of-atmosphere is -4.6 +/- 1.5 W/sq m for cloud-free and -2.1 +/- 0.7 W/sq m for all-sky conditions, during year 2006. These fluxes are consistent with, albeit generally less negative over ocean than, former assessments. Unlike previous studies, our estimate is constrained by retrievals of global coverage SSA, which may justify different DREA values. Remarkable consistency is found in comparison with DREA based on CERES (Clouds and the Earth's Radiant Energy System) and MODIS observations.

  6. Vertical Profiles of Aerosol Optical Properties Over Central Illinois and Comparison with Surface and Satellite Measurements

    Science.gov (United States)

    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.

  7. Aerosol indirect effects – general circulation model intercomparison and evaluation with satellite data

    Directory of Open Access Journals (Sweden)

    M. Schulz

    2009-11-01

    Full Text Available Aerosol indirect effects continue to constitute one of the most important uncertainties for anthropogenic climate perturbations. Within the international AEROCOM initiative, the representation of aerosol-cloud-radiation interactions in ten different general circulation models (GCMs is evaluated using three satellite datasets. The focus is on stratiform liquid water clouds since most GCMs do not include ice nucleation effects, and none of the model explicitly parameterises aerosol effects on convective clouds. We compute statistical relationships between aerosol optical depth (τa and various cloud and radiation quantities in a manner that is consistent between the models and the satellite data. It is found that the model-simulated influence of aerosols on cloud droplet number concentration (Nd compares relatively well to the satellite data at least over the ocean. The relationship between τa and liquid water path is simulated much too strongly by the models. This suggests that the implementation of the second aerosol indirect effect mainly in terms of an autoconversion parameterisation has to be revisited in the GCMs. A positive relationship between total cloud fraction (fcld and τa as found in the satellite data is simulated by the majority of the models, albeit less strongly than that in the satellite data in most of them. In a discussion of the hypotheses proposed in the literature to explain the satellite-derived strong fcld–τa relationship, our results indicate that none can be identified as a unique explanation. Relationships similar to the ones found in satellite data between τa and cloud top temperature or outgoing long-wave radiation (OLR are simulated by only a few GCMs. The GCMs that simulate a negative OLR–τa relationship show a strong positive correlation between

  8. Aerosol indirect effects ? general circulation model intercomparison and evaluation with satellite data

    Energy Technology Data Exchange (ETDEWEB)

    Quaas, Johannes; Ming, Yi; Menon, Surabi; Takemura, Toshihiko; Wang, Minghuai; Penner, Joyce E.; Gettelman, Andrew; Lohmann, Ulrike; Bellouin, Nicolas; Boucher, Olivier; Sayer, Andrew M.; Thomas, Gareth E.; McComiskey, Allison; Feingold, Graham; Hoose, Corinna; Kristansson, Jon Egill; Liu, Xiaohong; Balkanski, Yves; Donner, Leo J.; Ginoux, Paul A.; Stier, Philip; Grandey, Benjamin; Feichter, Johann; Sednev, Igor; Bauer, Susanne E.; Koch, Dorothy; Grainger, Roy G.; Kirkevag, Alf; Iversen, Trond; Seland, Oyvind; Easter, Richard; Ghan, Steven J.; Rasch, Philip J.; Morrison, Hugh; Lamarque, Jean-Francois; Iacono, Michael J.; Kinne, Stefan; Schulz, Michael

    2010-03-12

    Aerosol indirect effects continue to constitute one of the most important uncertainties for anthropogenic climate perturbations. Within the international AEROCOM initiative, the representation of aerosol-cloud-radiation interactions in ten different general circulation models (GCMs) is evaluated using three satellite datasets. The focus is on stratiform liquid water clouds since most GCMs do not include ice nucleation effects, and none of the model explicitly parameterises aerosol effects on convective clouds. We compute statistical relationships between aerosol optical depth ({tau}{sub a}) and various cloud and radiation quantities in a manner that is consistent between the models and the satellite data. It is found that the model-simulated influence of aerosols on cloud droplet number concentration (N{sub d}) compares relatively well to the satellite data at least over the ocean. The relationship between {tau}{sub a} and liquid water path is simulated much too strongly by the models. This suggests that the implementation of the second aerosol indirect effect mainly in terms of an autoconversion parameterisation has to be revisited in the GCMs. A positive relationship between total cloud fraction (f{sub cld}) and {tau}{sub a} as found in the satellite data is simulated by the majority of the models, albeit less strongly than that in the satellite data in most of them. In a discussion of the hypotheses proposed in the literature to explain the satellite-derived strong f{sub cld} - {tau}{sub a} relationship, our results indicate that none can be identified as a unique explanation. Relationships similar to the ones found in satellite data between {tau}{sub a} and cloud top temperature or outgoing long-wave radiation (OLR) are simulated by only a few GCMs. The GCMs that simulate a negative OLR - {tau}{sub a} relationship show a strong positive correlation between {tau}{sub a} and f{sub cld} The short-wave total aerosol radiative forcing as simulated by the GCMs is

  9. Synergy of Satellite-Surface Observations for Studying the Properties of Absorbing Aerosols in Asia

    Science.gov (United States)

    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

  10. Improvements to the retrieval of tropospheric NO2 from satellitestratospheric correction using SCIAMACHY limb/nadir matching and comparison to Oslo CTM2 simulations

    Directory of Open Access Journals (Sweden)

    A. Hilboll

    2013-03-01

    Full Text Available Satellite measurements of atmospheric trace gases have proved to be an invaluable tool for monitoring the Earth system. When these measurements are to be used for assessing tropospheric emissions and pollution, as for example in the case of nadir measurements of nitrogen dioxide (NO2, it is necessary to separate the stratospheric from the tropospheric signal. The SCIAMACHY instrument offers the unique opportunity to combine its measurements in limb- and nadir-viewing geometries into a tropospheric data product, using the limb measurements of the stratospheric NO2 abundances to correct the nadir measurements' total columns. In this manuscript, we present a novel approach to limb/nadir matching, calculating one stratospheric NO2 value from limb measurements for every single nadir measurement, abandoning global coverage for the sake of spatial accuracy. For comparison, modelled stratospheric NO2 columns from the Oslo CTM2 are also evaluated for stratospheric correction. Our study shows that stratospheric NO2 columns from SCIAMACHY limb measurements very well reflect stratospheric conditions. The zonal variability of the stratospheric NO2 field is captured by our matching algorithm, and the quality of the resulting tropospheric NO2 columns improves considerably. Both stratospheric datasets need to be adjusted to the level of the nadir measurements, because a time- and latitude-dependent bias to the measured nadir columns can be observed over clean regions. After this offset is removed, the two datasets agree remarkably well, and both stratospheric correction methods provide a significant improvement to the retrieval of tropospheric NO2 columns from the SCIAMACHY instrument.

  11. Constraining cloud lifetime effects of aerosols using A-Train satellite observations

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Minghuai; Ghan, Steven J.; Liu, Xiaohong; Ecuyer, Tristan L.; Zhang, Kai; Morrison, H.; Ovchinnikov, Mikhail; Easter, Richard C.; Marchand, Roger; Chand, Duli; Qian, Yun; Penner, Joyce E.

    2012-08-15

    Aerosol indirect effects have remained the largest uncertainty in estimates of the radiative forcing of past and future climate change. Observational constraints on cloud lifetime effects are particularly challenging since it is difficult to separate aerosol effects from meteorological influences. Here we use three global climate models, including a multi-scale aerosol-climate model PNNL-MMF, to show that the dependence of the probability of precipitation on aerosol loading, termed the precipitation frequency susceptibility (S{sub pop}), is a good measure of the liquid water path response to aerosol perturbation ({lambda}), as both Spop and {lambda} strongly depend on the magnitude of autoconversion, a model representation of precipitation formation via collisions among cloud droplets. This provides a method to use satellite observations to constrain cloud lifetime effects in global climate models. S{sub pop} in marine clouds estimated from CloudSat, MODIS and AMSR-E observations is substantially lower than that from global climate models and suggests a liquid water path increase of less than 5% from doubled cloud condensation nuclei concentrations. This implies a substantially smaller impact on shortwave cloud radiative forcing (SWCF) over ocean due to aerosol indirect effects than simulated by current global climate models (a reduction by one-third for one of the conventional aerosol-climate models). Further work is needed to quantify the uncertainties in satellite-derived estimates of S{sub pop} and to examine S{sub pop} in high-resolution models.

  12. A long-term satellite study of aerosol effects on convective clouds in Nordic background air

    Directory of Open Access Journals (Sweden)

    M. K. Sporre

    2013-05-01

    Full Text Available Aerosol-cloud interactions constitute a~major uncertainty in future climate predictions. This study combines 10 yr of ground-based aerosol particle measurements from 2 Nordic background stations (Vavihill and Hyytiälä with MODIS (Moderate Resolution Imaging Spectroradiometer satellite data of convective clouds. The merged data are used to examine the indirect aerosol effects on convective clouds over the Nordic countries. From the satellite scenes, vertical profiles of cloud droplet effective radius (re are created by plotting re against cloud top temperature. The profiles have been divided according to aerosol loading but also modeled meteorological parameters from the ECMWF (European Centre for Medium-Range Forecasts. Furthermore, weather radar data from the BALTEX (Baltic Sea Experiment and ground based precipitation measurements from several ground-based meteorological measurement stations have been investigated to determine whether aerosols affect precipitation intensity and amount. Higher aerosol number concentrations result in smaller re throughout the entire profiles at both stations. Profiles associated with no or little precipitation have smaller droplets than those associated with more precipitation. Furthermore, an increase in aerosol loadings results in a suppression of precipitation rates, when the vertical extent of the clouds has been taken into account. Clouds with greater vertical extent have the highest precipitation rates and are most sensitive to aerosol perturbations. Nevertheless, meteorological parameters such as the vertical extent of the clouds, the atmospheric instability and the relative humidity in the lower atmosphere affect the amount of precipitation that reaches the ground more than the aerosols do. The combination of these ground-based and remote sensing datasets provides a unique long-term study of the effects of aerosols on convective clouds over the Nordic countries.

  13. Satellite remote sensing of Asian aerosols: a case study of clean, polluted, and Asian dust storm days

    Directory of Open Access Journals (Sweden)

    K. H. Lee

    2010-12-01

    Full Text Available In East Asia, satellite observation is important because aerosols from natural and anthropogenic sources have been recognized as a major source of regional and global air pollution. However, retrieving aerosols properties from satellite observations over land can be difficult because of the surface reflection, complex aerosol composition, and aerosol absorption. In this study, a new aerosol retrieval method called as the Moderate Resolution Imaging Spectroradiometer (MODIS satellite aerosol retrieval (MSTAR was developed and applied to three different aerosol event cases over East Asia. MSTAR uses a separation technique that can distinguish aerosol reflectance from top-of-atmosphere (TOA reflectance. The aerosol optical thickness (AOT was determined by comparing this aerosol reflectance with pre-calculated values. Three case studies show how the methodology identifies discrepancies between measured and calculated values to retrieve more accurate AOT. The comparison between MODIS and the Aerosol Robotic Network (AERONET showed improvement using the suggested methodology with the cluster-based look-up-tables (LUTs (linear slope = 0.94, R = 0.92 than using operational MODIS collection 5 aerosol products (linear slope = 0.78, R = 0.87. In conclusion, the suggested methodology is shown to work well with aerosol models acquired by statistical clustering of the observation data in East Asia.

  14. Studies on aerosol properties during ICARB–2006 campaign period at Hyderabad, India using ground-based measurements and satellite data

    Indian Academy of Sciences (India)

    K V S Badarinath; Shailesh Kumar Kharol

    2008-07-01

    Continuous and campaign-based aerosol field measurements are essential in understanding fundamental atmospheric aerosol processes and for evaluating their effect on global climate, environment and human life. Synchronous measurements of Aerosol Optical Depth (AOD), Black Carbon (BC) aerosol mass concentration and aerosol particle size distribution were carried out during the campaign period at tropical urban regions of Hyderabad, India. Daily satellite datasets of DMSP-OLS were processed for night-time forest fires over the Indian region in order to understand the additional sources (forest fires) of aerosol. The higher values in black carbon aerosol mass concentration and aerosol optical depth correlated well with forest fires occurring over the region. Ozone Monitoring Instrument (OMI) aerosol index (AI) variations showed absorbing aerosols over the region and correlated with ground measurements.

  15. An Emerging Global Aerosol Climatology from the MODIS Satellite Sensors

    Science.gov (United States)

    Remer, Lorraine A.; Kleidman, Richard G.; Levy, Robert C.; Kaufman, Yoram J.; Tanre, Didier; Mattoo, Shana; Martins, J. Vandelei; Ichoku, Charles; Koren, Ilan; Hongbin, Yu; hide

    2008-01-01

    The recently released Collection 5 MODIS aerosol products provide a consistent record of the Earth's aerosol system. Comparison with ground-based AERONET observations of aerosol optical depth (AOD) we find that Collection 5 MODIS aerosol products estimate AOD to within expected accuracy more than 60% of the time over ocean and more than 72% of the time over land. This is similar to previous results for ocean, and better than the previous results for land. However, the new Collection introduces a 0.01 5 offset between the Terra and Aqua global mean AOD over ocean, where none existed previously. Aqua conforms to previous values and expectations while Terra is high. The cause of the offset is unknown, but changes to calibration are a possible explanation. We focus the climatological analysis on the better understood Aqua retrievals. We find that global mean AOD at 550 nm over oceans is 0.13 and over land 0.19. AOD in situations with 80% cloud fraction are twice the global mean values, although such situations occur only 2% of the time over ocean and less than 1% of the time over land. There is no drastic change in aerosol particle size associated with these very cloudy situations. Regionally, aerosol amounts vary from polluted areas such as East Asia and India, to the cleanest regions such as Australia and the northern continents. In almost all oceans fine mode aerosol dominates over dust, except in the tropical Atlantic downwind of the Sahara and in some months the Arabian Sea.

  16. Satellite-based estimate of aerosol direct radiative effect over the South-East Atlantic

    Directory of Open Access Journals (Sweden)

    L. Costantino

    2013-09-01

    Full Text Available The net effect of aerosol Direct Radiative Forcing (DRF is the balance between the scattering effect that reflects solar radiation back to space (cooling, and the absorption that decreases the reflected sunlight (warming. The amplitude of these two effects and their balance depends on the aerosol load, its absorptivity, the cloud fraction and the respective position of aerosol and cloud layers. In this study, we use the information provided by CALIOP (CALIPSO satellite and MODIS (AQUA satellite instruments as input data to a Rapid Radiative Transfer Model (RRTM and quantify the shortwave (SW aerosol direct atmospheric forcing, over the South-East Atlantic. The combination of the passive and active measurements allows estimates of the horizontal and vertical distributions of the aerosol and cloud parameters. We use a parametrization of the Single Scattering Albedo (SSA based on the satellite-derived Angstrom coefficient. The South East Atlantic is a particular region, where bright stratocumulus clouds are often topped by absorbing smoke particles. Results from radiative transfer simulations confirm the similar amplitude of the cooling effect, due to light scattering by the aerosols, and the warming effect, due to the absorption by the same particles. Over six years of satellite retrievals, from 2005 to 2010, the South-East Atlantic all-sky SW DRF is −0.03 W m−2, with a spatial standard deviation of 8.03 W m−2. In good agreement with previous estimates, statistics show that a cloud fraction larger than 0.5 is generally associated with positive all-sky DRF. In case of cloudy-sky and aerosol located only above the cloud top, a SSA larger than 0.91 and cloud optical thickness larger than 4 can be considered as threshold values, beyond which the resulting radiative forcing becomes positive.

  17. Seasonal persistence of ozone and zonal wind anomalies in the equatorial stratosphere

    OpenAIRE

    Tegtmeier, S.; V. E. Fioletov; Shepherd, T. G.

    2010-01-01

    Analysis of the variability of equatorial ozone profiles in the Satellite Aerosol and Gas Experiment-corrected Solar Backscatter Ultraviolet data set demonstrates a strong seasonal persistence of interannual ozone anomalies, revealing a seasonal dependence to equatorial ozone variability. In the lower stratosphere (40–25 hPa) and in the upper stratosphere (6–4 hPa), ozone anomalies persist from approximately November until June of the following year, while ozone anomalies in the layer between...

  18. Impact of idealized future stratospheric aerosol injection on the large-scale ocean and land carbon cycles

    Science.gov (United States)

    Tjiputra, J. F.; Grini, A.; Lee, H.

    2016-01-01

    Using an Earth system model, we simulate stratospheric aerosol injection (SAI) on top of the Representative Concentration Pathways 8.5 future scenario. Our idealized method prescribes aerosol concentration, linearly increasing from 2020 to 2100, and thereafter remaining constant until 2200. In the aggressive scenario, the model projects a cooling trend toward 2100 despite warming that persists in the high latitudes. Following SAI termination in 2100, a rapid global warming of 0.35 K yr-1 is simulated in the subsequent 10 years, and the global mean temperature returns to levels close to the reference state, though roughly 0.5 K cooler. In contrast to earlier findings, we show a weak response in the terrestrial carbon sink during SAI implementation in the 21st century, which we attribute to nitrogen limitation. The SAI increases the land carbon uptake in the temperate forest-, grassland-, and shrub-dominated regions. The resultant lower temperatures lead to a reduction in the heterotrophic respiration rate and increase soil carbon retention. Changes in precipitation patterns are key drivers for variability in vegetation carbon. Upon SAI termination, the level of vegetation carbon storage returns to the reference case, whereas the soil carbon remains high. The ocean absorbs nearly 10% more carbon in the geoengineered simulation than in the reference simulation, leading to a ˜15 ppm lower atmospheric CO2 concentration in 2100. The largest enhancement in uptake occurs in the North Atlantic. In both hemispheres' polar regions, SAI delays the sea ice melting and, consequently, export production remains low. In the deep water of North Atlantic, SAI-induced circulation changes accelerate the ocean acidification rate and broaden the affected area.

  19. Intercomparison of daytime stratospheric NO2 satellite retrievals and model simulations

    Science.gov (United States)

    Belmonte Rivas, M.; Veefkind, P.; Boersma, F.; Levelt, P.; Eskes, H.; Gille, J.

    2014-07-01

    This paper evaluates the agreement between stratospheric NO2 retrievals from infrared limb sounders (Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) and High Resolution Dynamics Limb Sounder (HIRDLS)) and solar UV/VIS backscatter sensors (Ozone Monitoring Instrument (OMI), Scanning Imaging Absorption Spectrometer for Atmospheric Cartography (SCIAMACHY) limb and nadir) over the 2005-2007 period and across the seasons. The observational agreement is contrasted with the representation of NO2 profiles in 3-D chemical transport models such as the Whole Atmosphere Community Climate Model (WACCM) and TM4. A conclusion central to this work is that the definition of a reference for stratospheric NO2 columns formed by consistent agreement among SCIAMACHY, MIPAS and HIRDLS limb records (all of which agree to within 0.25 × 1015 molecules cm-2 or better than 10%) allows us to draw attention to relative errors in other data sets, e.g., (1) WACCM overestimates NO2 densities in the extratropical lower stratosphere, particularly in the springtime and over northern latitudes by up to 35% relative to limb observations, and (2) there are remarkable discrepancies between stratospheric NO2 column estimates from limb and nadir techniques, with a characteristic seasonally and latitudinally dependent pattern. We find that SCIAMACHY nadir and OMI stratospheric columns show overall biases of -0.5 × 1015 molecules cm-2 (-20%) and +0.6 × 1015 molecules cm-2 (+20%) relative to limb observations, respectively. It is argued that additive biases in nadir stratospheric columns are not expected to affect tropospheric retrievals significantly, and that they can be attributed to errors in the total slant column density, related either to algorithmic or instrumental effects. In order to obtain accurate and long-term time series of stratospheric NO2, an effort towards the harmonization of currently used differential optical absorption spectroscopy (DOAS) approaches to nadir

  20. Effect of tropical cyclones on the stratosphere-troposphere exchange observed using satellite observations over the north Indian Ocean

    Science.gov (United States)

    Venkat Ratnam, M.; Babu, S. Ravindra; Das, S. S.; Basha, G.; Krishnamurthy, B. V.; Venkateswararao, B.

    2016-07-01

    Tropical cyclones play an important role in modifying the tropopause structure and dynamics as well as stratosphere-troposphere exchange (STE) processes in the upper troposphere and lower stratosphere (UTLS) region. In the present study, the impact of cyclones that occurred over the north Indian Ocean during 2007-2013 on the STE processes is quantified using satellite observations. Tropopause characteristics during cyclones are obtained from the Global Positioning System (GPS) radio occultation (RO) measurements, and ozone and water vapour concentrations in the UTLS region are obtained from Aura Microwave Limb Sounder (MLS) satellite observations. The effect of cyclones on the tropopause parameters is observed to be more prominent within 500 km of the centre of the tropical cyclone. In our earlier study, we observed a decrease (increase) in the tropopause altitude (temperature) up to 0.6 km (3 K), and the convective outflow level increased up to 2 km. This change leads to a total increase in the tropical tropopause layer (TTL) thickness of 3 km within 500 km of the centre of cyclone. Interestingly, an enhancement in the ozone mixing ratio in the upper troposphere is clearly noticed within 500 km from the cyclone centre, whereas the enhancement in the water vapour in the lower stratosphere is more significant on the south-east side, extending from 500 to 1000 km away from the cyclone centre. The cross-tropopause mass flux for different intensities of cyclones is estimated and it is found that the mean flux from the stratosphere to the troposphere for cyclonic storms is 0.05 ± 0.29 × 10-3 kg m-2, and for very severe cyclonic storms it is 0.5 ± 1.07 × 10-3 kg m-2. More downward flux is noticed on the north-west and south-west side of the cyclone centre. These results indicate that the cyclones have significant impact in effecting the tropopause structure, ozone and water vapour budget, and consequentially the STE in the UTLS region.

  1. Quantifying Above-Cloud Aerosols through Integrating Multi-Sensor Measurements from A-Train Satellites

    Science.gov (United States)

    Zhang, Yan

    2012-01-01

    Quantifying above-cloud aerosols can help improve the assessment of aerosol intercontinental transport and climate impacts. Large-scale measurements of aerosol above low-level clouds had been generally unexplored until very recently when CALIPSO lidar started to acquire aerosol and cloud profiles in June 2006. Despite CALIPSO s unique capability of measuring above-cloud aerosol optical depth (AOD), such observations are substantially limited in spatial coverage because of the lidar s near-zero swath. We developed an approach that integrates measurements from A-Train satellite sensors (including CALIPSO lidar, OMI, and MODIS) to extend CALIPSO above-cloud AOD observations to substantially larger areas. We first examine relationships between collocated CALIPSO above-cloud AOD and OMI absorbing aerosol index (AI, a qualitative measure of AOD for elevated dust and smoke aerosol) as a function of MODIS cloud optical depth (COD) by using 8-month data in the Saharan dust outflow and southwest African smoke outflow regions. The analysis shows that for a given cloud albedo, above-cloud AOD correlates positively with AI in a linear manner. We then apply the derived relationships with MODIS COD and OMI AI measurements to derive above-cloud AOD over the whole outflow regions. In this talk, we will present spatial and day-to-day variations of the above-cloud AOD and the estimated direct radiative forcing by the above-cloud aerosols.

  2. Three-dimensional structure of aerosol in China: A perspective from multi-satellite observations

    Science.gov (United States)

    Guo, Jianping; Liu, Huan; Wang, Fu; Huang, Jingfeng; Xia, Feng; Lou, Mengyun; Wu, Yerong; Jiang, Jonathan H.; Xie, Tao; Zhaxi, Yangzong; Yung, Yuk L.

    2016-09-01

    Using eight years (2006-2014) of passive (MODIS/Aqua and OMI/Aura) and active (CALIOP/CALIPSO) satellite measurements of aerosols, we yield a three-dimensional (3D) distribution of the frequency of occurrence (FoO) of aerosols over China. As an indicator of the vertical heterogeneity of aerosol layers detected by CALIOP, two types of Most Probable Height (MPH), including MPH_FoO and MPH_AOD, are deduced. The FoO of "Total Aerosol" reveals significant geographical dependence. Eastern China showed much stronger aerosol FoD than northwestern China. The FoO vertical structures of aerosol layer are strongly dependent on altitudes. Among the eight typical ROIs analyzed, aerosol layers over the Gobi Desert have the largest occurrence probability located at an altitude as high as 2.83 km, as compared to 1.26 km over Beijing-Tianjin-Hebei. The diurnal variation (nighttime-daytime) in MPH_AOD varies from an altitude as low as 0.07 km over the Sichuan basin to 0.27 km over the Gobi Desert, whereas the magnitude of the diurnal variation in terms of MPH_AOD is six times as large as the MPH_FoO, mostly attributable to the day/night lidar SNR difference. Also, the 3D distribution of dust and smoke aerosols was presented. The multi-sensor synergized 3D observations of dust aerosols, frequently observed in the zonal belt of 38°N-45°N, is markedly different from that of smoke aerosols that are predominantly located in the eastern and southern parts. The 3D FoO distribution of dust indicates a west-to-east passageway of dust originating from the westernmost Taklimakan Desert all the way to North China Plain (NCP). The findings from the multi-sensor synergetic observations greatly improved our understanding on the long-range aerosol dispersion, transport and passageway over China.

  3. Validation of ACE-FTS satellite data in the upper troposphere/lower stratosphere (UTLS using non-coincident measurements

    Directory of Open Access Journals (Sweden)

    M. I. Hegglin

    2007-09-01

    Full Text Available CO, O3, and H2O data in the upper troposphere/lower stratosphere (UTLS measured by the Atmospheric Chemistry Experiment Fourier Transform Spectrometer (ACE-FTS on Canada's SCISAT-1 satellite are validated using aircraft measurements. In the UTLS, validation of chemical trace gas measurements is a challenging task due to small-scale variability in the tracer fields, strong gradients of the tracers across the tropopause, and scarcity of measurements suitable for validation purposes. Two alternative methods for the validation of the satellite data are introduced, which avoid the usual need for coincident measurements: tracer-tracer correlations, and vertical profiles relative to the tropopause height. Both largely reduce geophysical variability and thereby provide an "instantaneous climatology", allowing measurement comparison with non-coincident data which yields information about the precision, and a statistically meaningful error-assessment of the ACE-FTS satellite data. We found that the ACE-FTS CO and lower stratospheric O3 agree with the aircraft measurements within ±10% and ±5%, respectively. The ACE-FTS O3 in the UT exhibits a high bias of up to 40%. H2O indicates a low bias with relative differences of around 20% in the LS and 40% in the UT, respectively. When taking into account the smearing effect of the vertically limited spacing between measurements of the ACE-FTS instrument, the errors decrease by 5–15% around the tropopause. The ACE-FTS instrument hence offers unprecedented precision and vertical resolution in the UTLS, that will allow a new global perspective on UTLS tracer distributions.

  4. Stratospheric dryness

    Directory of Open Access Journals (Sweden)

    J. Lelieveld

    2006-11-01

    Full Text Available The mechanisms responsible for the extreme dryness of the stratosphere have been debated for decades. A key difficulty has been the lack of models which are able to reproduce the observations. Here we examine results from a new atmospheric chemistry general circulation model (ECHAM5/MESSy1 together with satellite observations. Our model results match observed temperatures in the tropical lower stratosphere and realistically represent recurrent features such as the semi-annual oscillation (SAO and the quasi-biennual oscillation (QBO, indicating that dynamical and radiation processes are simulated accurately. The model reproduces the very low water vapor mixing ratios (1–2 ppmv periodically observed at the tropical tropopause near 100 hPa, as well as the characteristic tape recorder signal up to about 10 hPa, providing evidence that the dehydration mechanism is well-captured, albeit that the model underestimates convective overshooting and consequent moistening events. Our results show that the entry of tropospheric air into the stratosphere at low latitudes is forced by large-scale wave dynamics; however, radiative cooling can regionally limit the upwelling or even cause downwelling. In the cold air above cumulonimbus anvils thin cirrus desiccates the air through the sedimentation of ice particles, similar to polar stratospheric clouds. Transport deeper into the stratosphere occurs in regions where radiative heating becomes dominant, to a large extent in the subtropics. During summer the stratosphere is moistened by the monsoon, most strongly over Southeast Asia.

  5. Investigating relationships between aerosol optical depth and cloud fraction using satellite, aerosol reanalysis and general circulation model data

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    B. S. Grandey

    2013-03-01

    Full Text Available Strong positive relationships between cloud fraction (fc and aerosol optical depth (τ have been reported. Data retrieved from the MODerate resolution Imaging Spectroradiometer (MODIS instrument show positive fc–τ relationships across most of the globe. A global mean fc increase of approximately 0.2 between low and high τ conditions is found for both ocean and land. However, these relationships are not necessarily due to cloud–aerosol interactions. Using state-of-the-art Monitoring Atmospheric Composition and Climate (MACC reanalysis-forecast τ data, which should be less affected by retrieval artefacts, it is demonstrated that a large part of the observed fc–τ signal may be due to cloud contamination of satellite-retrieved τ. For longer MACC forecast time steps of 24 h, which likely contain less cloud contamination, some negative fc–τ relationships are found. The global mean fc increase between low and high τ conditions is reduced to 0.1, suggesting that cloud contamination may account for approximately one half of the satellite-retrieved increase in fc. ECHAM5-HAM general circulation model (GCM simulations further demonstrate that positive fc–τ relationships may arise due to covariation with relative humidity. Widespread negative simulated fc–τ relationships in the tropics are shown to arise due to scavenging of aerosol by convective precipitation. Wet scavenging events are likely poorly sampled in satellite-retrieved data, because the properties of aerosol below clouds cannot be retrieved. Quantifying the role of wet scavenging, and assessing GCM representations of this important process, remains a challenge for future observational studies of aerosol–cloud–precipitation interactions.

  6. Latitudinal variations of aerosol optical parameters over South Africa based on MISR satellite data

    CSIR Research Space (South Africa)

    Tesfaye M

    2010-09-01

    Full Text Available The latitudunal variation of the relative weight size distribution and optical properties of aerosols over South Africa is presented here. The study uses 10-years of Multi-angle Imaging SpectroRadiometer (MISR) satellite data, collected over South...

  7. Retrieval of aerosol optical depth for Chongqing using the HJ-1 satellite data

    Science.gov (United States)

    Wang, Zengwu; Yang, Shiqi; Zeng, Qiaolin; Wang, Yongqian

    2017-06-01

    Aerosol optical depth (AOD) is a common indicator applied in monitoring aerosols in the atmosphere. The hilly landscape and rapid economic growth of the megacity Chongqing have facilitated increased aerosol concentration, and it is meaningful to accurately retrieve AOD over Chongqing. The HJ-1A/B satellite of China carries a sensor/camera called the Charge Coupled Device (CCD), the spatial resolution of which meets the requirement for retrieving high resolution AOD. In this paper, analysis of the AOD retrievals from different methods using the HJ-1 satellite data revealed the most suitable algorithm. Through comparison with the AOD product of Moderate Resolution Imaging Spectroradiometer (MODIS), the AOD retrieval results using enhanced vegetation index (EVI) to estimate dark pixels showed the highest correlation. The continental aerosol model was used to build a lookup table that was able to facilitate a good AOD retrieval for both city and rural areas. Finally, the algorithm that combined dark pixels, buffer areas, and the deep blue algorithm was found to be most suitable for AOD retrieval. The AOD retrieval results based on the HJ-1 data were consistent with MODIS products, and our algorithm yields reasonable results in most cases. The results were also compared with ground-based PM10 measurements synchronized with the overpass time of the HJ-1 satellite, and high correlation was found. The findings are relevant to other Chinese satellite data used for retrieving AOD on the same channels.

  8. Implications of Satellite Swath Width on Global Aerosol Optical Thickness Statistics

    Science.gov (United States)

    Colarco, Peter; Kahn, Ralph; Remer, Lorraine; Levy, Robert; Welton, Ellsworth

    2012-01-01

    We assess the impact of swath width on the statistics of aerosol optical thickness (AOT) retrieved by satellite as inferred from observations made by the Moderate Resolution Imaging Spectroradiometer (MODIS). We sub-sample the year 2009 MODIS data from both the Terra and Aqua spacecraft along several candidate swaths of various widths. We find that due to spatial sampling there is an uncertainty of approximately 0.01 in the global, annual mean AOT. The sub-sampled monthly mean gridded AOT are within +/- 0.01 of the full swath AOT about 20% of the time for the narrow swath sub-samples, about 30% of the time for the moderate width sub-samples, and about 45% of the time for the widest swath considered. These results suggest that future aerosol satellite missions with only a narrow swath view may not sample the true AOT distribution sufficiently to reduce significantly the uncertainty in aerosol direct forcing of climate.

  9. Remote Sensing of Aerosols from Satellites: Why Has It Been Do Difficult to Quantify Aerosol-Cloud Interactions for Climate Assessment, and How Can We Make Progress?

    Science.gov (United States)

    Kahn, Ralph A.

    2015-01-01

    The organizers of the National Academy of Sciences Arthur M. Sackler Colloquia Series on Improving Our Fundamental Understanding of the Role of Aerosol-Cloud Interactions in the Climate System would like to post Ralph Kahn's presentation entitled Remote Sensing of Aerosols from Satellites: Why has it been so difficult to quantify aerosol-cloud interactions for climate assessment, and how can we make progress? to their public website.

  10. Some implications of sampling choices on comparisons between satellite and model aerosol optical depth fields

    Directory of Open Access Journals (Sweden)

    A. M. Sayer

    2010-11-01

    Full Text Available The comparison of satellite and model aerosol optical depth (AOD fields provides useful information on the strengths and weaknesses of both. However, the sampling of satellite and models is very different and some subjective decisions about data selection and aggregation must be made in order to perform such comparisons. This work examines some implications of these decisions, using GlobAerosol AOD retrievals at 550 nm from Advanced Along-Track Scanning Radiometer (AATSR measurements, and aerosol fields from the GEOS-Chem chemistry transport model. It is recommended to sample the model only where the satellite flies over on a particular day; neglecting this can cause regional differences in model AOD of up to 0.1 on monthly and annual timescales. The comparison is observed to depend strongly upon thresholds for sparsity of satellite retrievals in the model grid cells. Requiring at least 25% coverage of the model grid cell by satellite data decreases the observed difference between the two by approximately half over land. The impact over ocean is smaller. In both model and satellite datasets, there is an anticorrelation between the proportion p of a model grid cell covered by satellite retrievals and the AOD. This is attributed to small p typically occuring due to high cloud cover and lower AODs being found in large clear-sky regions. Daily median AATSR AODs were found to be closer to GEOS-Chem AODs than daily means (with the root mean squared difference being approximately 0.05 smaller. This is due to the decreased sensitivity of medians to outliers such as cloud-contaminated retrievals, or aerosol point sources not included in the model.

  11. Direct radiative forcing of aerosols in cloudy condition using CALIPSO satellite data

    Science.gov (United States)

    Oikawa, E.; Nakajima, T.; Winker, D. M.

    2013-12-01

    The aerosol direct effect occurs by direct scattering and absorption of solar and thermal radiation. Shortwave direct aerosol radiative forcing (DARF) under clear-sky condition is estimated about 5 Wm-2 from satellite retrievals and model simulations [Yu et al., 2006ACP]. Simultaneous observations of aerosols and clouds are very limited, thus it is difficult to validate the estimation of DARF under cloudy-sky condition. In 2006, the CALIPSO (Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observations) satellite was launched with the space-borne lidar, CALIOP (Cloud-Aerosol Lidar with Orthogonal Polarization). This enabled us to get data of the vertical distribution of aerosols and clouds all over the world. Oikawa et al. [2013JGR] estimated DARF under clear-sky, cloudy-sky, and all-sky conditions using CALIPSO and MODIS (Moderate resolution Imaging Spectrometer) data. Over Atlantic Ocean off southwest Africa, biomass burning aerosols are transported above low-level clouds and cause large positive DARF [Oikawa et al., 2013JGR; Chand et al., 2009Nat. Geosci.; De Graaf et al., 2012JGR; Takemura et al., 2005JGR]. We calculate DARF using CALIOP Level 2 Cloud and Aerosol Layer Products Version 3 and the method of Oikawa et al. [2013]. In this study, we focus on the case that aerosols exist above clouds (above-cloud case) in 2007. Over Atlantic Ocean off southwest Africa, DARF caused by smoke aerosols is +7.1 Wm-2 in September. On the other hand, aerosol optical thickness (AOT) of smoke is small as close to 0 Wm-2 in spring season. Over North Pacific, yellow sand and industrial smoke are transported from Asia and DARF is +5.2 Wm-2 in May. Dust AOT at 532 nm is 0.014 and polluted dust AOT at 532 nm is 0.052; in other words, a large part of dust emitted from Taklamakan and Gobi deserts are mixed with the industrial smoke and transported to the Pacific Ocean according to the CALIPSO algorithms.

  12. Comparing regional modeling (CHIMERE) and satellite observations of aerosols (PARASOL): Methodology and case study over Mexico

    Science.gov (United States)

    Stromatas, Stavros

    2010-05-01

    S. Stromatas (1), S. Turquety (1), H. Chepfer (1), L. Menut (1), B. Bessagnet (2), JC Pere (2), D. Tanré (3) . (1) Laboratoire de Météorologie Dynamique, CNRS/IPSL, École Polytechnique, 91128 Palaiseau Cedex, France, (2) INERIS, Institut National de l'Environnement Industriel et des Risques, Parc technologique ALATA, 60550 Verneuil en Halatte, FRANCE, (3) Laboratoire d'Optique Atmosphérique/CNRS Univ. des Sciences et Tech. de Lille, 59650 - Villeneuve d'Ascq, France. Atmospheric suspended particles (aerosols) have significant radiative and environmental impacts, affecting human health, visibility and climate. Therefore, they are regulated by air quality standards worldwide, and monitored by regional observation networks. Satellite observations vastly improve the horizontal and temporal coverage, providing daily distributions. Aerosols are currently estimated using aerosol optical depth (AOD) retrievals, a quantitative measure of the extinction of solar radiation by aerosol scattering and absorption between the point of observation and the top of the atmosphere. Even though remarkable progresses in aerosol modeling by chemistry-transport models (CTM) and measurement experiments have been made in recent years, there is still a significant divergence between the modeled and observed results. However, AOD retrievals from satellites remains a highly challenging task mostly because it depends on a variety of different parameters such as cloud contamination, surface reflectance contributions and a priori assumptions on aerosol types, each one of them incorporating its own difficulties. Therefore, comparisons between CTM and observations are often difficult to interpret. In this presentation, we will discuss comparisons between regional modeling (CHIMERE CTM) over Mexico and satellite observations obtained by the POLDER instrument embarked on PARASOL micro-satellite. After a comparison of the model AOD with the retrieved L2 AOD, we will present an alternative

  13. Satellite observations of cirrus clouds in the Northern Hemisphere lowermost stratosphere

    Directory of Open Access Journals (Sweden)

    R. Spang

    2014-05-01

    Full Text Available Here we present observations of the Cryogenic Infrared Spectrometers and Telescopes for the Atmosphere (CRISTA of cirrus cloud and water vapour in August 1997 in the upper troposphere and lower stratosphere (UTLS region. The observations indicate a considerable flux of moisture from the upper tropical troposphere into the extra-tropical lowermost stratosphere (LMS, resulting in the occurrence of high altitude optically thin cirrus clouds in the LMS. The locations of the LMS cloud events observed by CRISTA are consistent with the tropopause height determined from coinciding radiosonde data. For a hemispheric analysis in tropopause relative coordinates an improved tropopause determination has been applied to the ECMWF temperature profiles. We found that a significant fraction of the cloud occurrences in the tropopause region are located in the LMS, even if a conservative overestimate of the cloud top height (CTH determination by CRISTA of 500 m is assumed. The results show rather high occurrence frequencies (∼5% up to high northern latitudes (70° N and altitudes well above the tropopause (>500 m at ∼350 K and above in large areas at mid and high latitudes. Comparisons with model runs of the Chemical Lagragian Model of the Stratosphere (CLaMS over the CRISTA period show a reasonable consistency for the retrieved cloud pattern. For this purpose a limb ray tracing approach was applied through the 3-D model fields to obtain integrated measurement information through the atmosphere along the limb path of the instrument. The simplified cirrus scheme implemented in CLaMS seems to cause a systematic underestimation in the CTH occurrence frequencies in the LMS with respect to the observations. The observations together with the model results demonstrate the importance of isentropic, quasi-horizontal transport of water vapour from the sub-tropics and the potential for the occurrence of cirrus clouds in the lowermost stratosphere and tropopause region.

  14. Observation operator for the assimilation of aerosol type resolving satellite measurements into a chemical transport model

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    M. Schroedter-Homscheidt

    2010-11-01

    Full Text Available Modelling of aerosol particles with chemical transport models is still based mainly on static emission databases while episodic emissions cannot be treated sufficiently. To overcome this situation, a coupling of chemical mass concentration modelling with satellite-based measurements relying on physical and optical principles has been developed. This study deals with the observation operator for a component-wise assimilation of satellite measurements. It treats aerosol particles classified into water soluble, water insoluble, soot, sea salt and mineral dust containing aerosol particles in the atmospheric boundary layer as separately assimilated aerosol components. It builds on a mapping of aerosol classes used both in observation and model space taking their optical and chemical properties into account. Refractive indices for primary organic carbon particles, anthropogenic particles, and secondary organic species have been defined based on a literature review. Together with a treatment of different size distributions in observations and model state, this allows transforming the background from mass concentrations into aerosol optical depths. A two-dimensional, variational assimilation is applied for component-wise aerosol optical depths. Error covariance matrices are defined based on a validation against AERONET sun photometer measurements. Analysis fields are assessed threefold: (1 through validation against AERONET especially in Saharan dust outbreak situations, (2 through comparison with the British Black Smoke and Sulphur Dioxide Network for soot-containing particles, and (3 through comparison with measurements of the water soluble components SO4, NH4, and NO3 conducted by the EMEP (European Monitoring and Evaluation Programme network. Separately, for the water soluble, the soot and the mineral dust aerosol components a bias reduction and subsequent a root mean square error reduction is observed in the

  15. Satellite Detection of Smoke Aerosols Over a Snow/Ice Surface by TOMS

    Science.gov (United States)

    Hsu, N. Christina; Herman, Jay R.; Gleason, J. F.; Torres, O.; Seftor, C. J.

    1998-01-01

    The use of TOMS (Total Ozone Mapping Spectrometer) satellite data demonstrates the recently developed technique of using satellite UV radiance measurements to detect absorbing tropospheric aerosols is effective over snow/ice surfaces. Instead of the traditional single wavelength (visible or infrared) method of measuring tropospheric aerosols, this method takes advantage of the wavelength dependent reduction in the backscattered radiance due to the presence of absorbing aerosols over snow/ice surfaces. An example of the resulting aerosol distribution derived from TOMS data is shown for an August 1998 event in which smoke generated by Canadian forest fires drifts over and across Greenland. As the smoke plume moved over Greenland, the TOMS observed 380 nm reflectivity over the snow/ice surface dropped drastically from 90-100% down to 30-40%. To study the effects of this smoke plume in both the UV and visible regions of the spectrum, we compared a smoke-laden spectrum taken over Greenland by the high spectral resolution (300 to 800 nm) GOME instrument with one that is aerosol-free. We also discuss the results of modeling the darkening effects of various types of absorbing aerosols over snow/ice surfaces using a radiative transfer code. Finally, we investigated the history of such events by looking at the nearly twenty year record of TOMS aerosol index measurements and found that there is a large interannual variability in the amount of smoke aerosols observed over Greenland. This information will be available for studies of radiation and transport properties in the Arctic.

  16. Characterization of intense aerosol episodes in the Mediterranean basin from satellite observations

    Science.gov (United States)

    Gkikas, Antonis; Hatzianastassiou, Nikos; Mihalopoulos, Nikolaos

    2014-05-01

    The properties and distribution of aerosols over the broader Mediterranean region are complex since particles of different nature are either produced within its boundaries or transported from other regions. Thus, coarse dust aerosols are transported primarily from Sahara and secondarily from Middle East, while fine polluted aerosols are either produced locally from anthropogenic activities or they are transported from neighbouring or remote European areas. Also during summer biomass aerosols are transported towards the Mediterranean, originating from massive and extended fires occurring in northern Balkans and Eastern Europe and favoured by the prevailing synoptic conditions. In addition, sea-salt aerosols originate from the Mediterranean Sea or the Atlantic Ocean. Occasionally, aerosols are encountered at very high concentrations (aerosol episodes or events) significantly affecting atmospheric dynamics and climate as well as human health. Given the coexistence of different aerosols as internal and external mixtures characterizing and discriminating between the different types of aerosol episodes is a big challenge. A characterization and classification of intense aerosol episodes in the Mediterranean basin (March 2000 - February 2007) is attempted in the present study. This is achieved by implementing an objective and dynamic algorithm which uses daily aerosol optical properties derived from satellite measurements, namely MODIS-Terra, Earth Probe (EP)-TOMS and OMI-Aura. The aerosol episodes are first classified into strong and extreme ones, according to their intensity, by means of aerosol optical depth at 550nm (AOD550nm). Subsequently, they are discriminated into the following aerosol types: (i) biomass/urban-industrial (BU), (ii) desert dust (DD), (iii) sea-salt like (SS), (iv) mixed (MX) and (v) undetermined (UN). The classification is based on aerosol optical properties accounting for the particles' size (Ångström exponent, Effective radius), the

  17. Vertical profiles of aerosol optical properties over central Illinois and comparison with surface and satellite measurements

    Directory of Open Access Journals (Sweden)

    P. J. Sheridan

    2012-12-01

    Full Text Available 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. The primary profile location was within 15 km of the NOAA/ESRL surface aerosol monitoring station near Bondville, Illinois. Identical instruments at the surface and on the aircraft ensured that the data from both platforms would be directly comparable and permitted a determination of how representative surface aerosol properties were of the lower column. Aircraft profiles were also conducted occasionally at two other nearby locations to increase the frequency of A-Train satellite underflights for the purpose of comparing in situ and satellite-retrieved aerosol data. Measurements of aerosol properties conducted at low relative humidity over the Bondville site compare well with the analogous surface aerosol data and do not indicate any major sampling issues or that the aerosol is radically different at the surface compared with the lowest flyby altitude of ~ 240 m above ground level. Statistical analyses of the in situ vertical profile data indicate that aerosol light scattering and absorption (related to aerosol amount decreases substantially with increasing altitude. Parameters related to the nature of the aerosol (e.g., single-scattering albedo, Ångström exponent, etc., however, are relatively constant throughout the mixed layer, and do not vary as much as the aerosol amount throughout the profile. While individual profiles often showed more variability, the median in situ single-scattering albedo was 0.93–0.95 for all sampled altitudes. Several parameters (e.g., submicrometer scattering fraction, hemispheric backscattering fraction, and

  18. A satellite view of the direct effect of aerosols on solar radiation at global scale

    Science.gov (United States)

    Hatzianastassiou, Nikolaos; Papadimas, Christos D.; Matsoukas, Christos; Fotiadi, Aggeliki; Benas, Nikolaos; Vardavas, Ilias

    2016-04-01

    Aerosols are a key parameter for better understanding and predicting current and future climate change. They are determining, apart from clouds, patterns of solar radiation through scattering and absorption processes. Especially, under cloud-free skies, aerosols are the major modulator of the solar radiation budget of the Earth-atmosphere system. Although significant improvement has been made as to better understanding the direct radiative effect (DRE) of aerosols, there is still a need for further improvement in our knowledge of the DRE spatial and temporal patterns, in particular with respect to extended spatial and temporal coverage of relevant information. In an ongoing rapidly evolving era of great satellite-based achievements, concerning the knowledge of solar radiation budget and its modulators, and with the great progress in obtaining significant information on key aerosol optical properties needed for modeling DRE, it is a great challenge to use all this new aerosol information and to see what is the new acquired scientific knowledge. The objective of this study is to obtain an improved view of global aerosol DRE effects using contemporary accurate data for the important atmospheric and surface parameters determining the solar radiation budget, with emphasis to state of the art aerosol data. Thus, a synergy is made of different datasets providing the necessary input data and of a detailed spectral radiative transfer model (RTM) to compute spectral globally distributed aerosol DREs. Emphasis is given on using highly accurate and well-tested aerosol optical properties. Spectral information on aerosol optical depth (AOD) is taken from retrieved products of the MODerate resolution Imaging Spectroradiometer (MODIS) instrument, while similar information is taken from MODIS for the aerosol asymmetry parameter (AP) over ocean. Information from MODIS is also taken for the aerosol single scattering albedo (SSA). All this information comes from the latest Collection

  19. Testing the MODIS Satellite Retrieval of Aerosol Fine-Mode Fraction

    Science.gov (United States)

    Anderson, Theodore L.; Wu, Yonghua; Chu, D. Allen; Schmid, Beat; Redemann, Jens; Dubovik, Oleg

    2005-01-01

    Satellite retrievals of the fine-mode fraction (FMF) of midvisible aerosol optical depth, tau, are potentially valuable for constraining chemical transport models and for assessing the global distribution of anthropogenic aerosols. Here we compare satellite retrievals of FMF from the Moderate Resolution Imaging Spectroradiometer (MODIS) to suborbital data on the submicrometer fraction (SMF) of tau. SMF is a closely related parameter that is directly measurable by in situ techniques. The primary suborbital method uses in situ profiling of SMF combined with airborne Sun photometry both to validate the in situ estimate of ambient extinction and to take into account the aerosol above the highest flight level. This method is independent of the satellite retrieval and has well-known accuracy but entails considerable logistical and technical difficulties. An alternate method uses Sun photometer measurements near the surface and an empirical relation between SMF and the Angstrom exponent, A, a measure of the wavelength dependence of optical depth or extinction. Eleven primary and fifteen alternate comparisons are examined involving varying mixtures of dust, sea salt, and pollution in the vicinity of Korea and Japan. MODIS ocean retrievals of FMF are shown to be systematically higher than suborbital estimates of SMF by about 0.2. The most significant cause of this discrepancy involves the relationship between 5 and fine-mode partitioning; in situ measurements indicate a systematically different relationship from what is assumed in the satellite retrievals. Based on these findings, we recommend: (1) satellite programs should concentrate on retrieving and validating since an excellent validation program is in place for doing this, and (2) suborbital measurements should be used to derive relationships between A and fine-mode partitioning to allow interpretation of the satellite data in terms of fine-mode aerosol optical depth.

  20. Detection of deep stratospheric intrusions by cosmogenic 35S

    Science.gov (United States)

    Lin, Mang; Su, Lin; Shaheen, Robina; Fung, Jimmy C. H.; Thiemens, Mark H.

    2016-10-01

    The extent to which stratospheric intrusions on synoptic scales influence the tropospheric ozone (O3) levels remains poorly understood, because quantitative detection of stratospheric air has been challenging. Cosmogenic 35S mainly produced in the stratosphere has the potential to identify stratospheric air masses at ground level, but this approach has not yet been unambiguously shown. Here, we report unusually high 35S concentrations (7,390 atoms m-3; ˜16 times greater than annual average) in fine sulfate aerosols (aerodynamic diameter less than 0.95 µm) collected at a coastal site in southern California on May 3, 2014, when ground-level O3 mixing ratios at air quality monitoring stations across southern California (43 of 85) exceeded the recently revised US National Ambient Air Quality Standard (daily maximum 8-h average: 70 parts per billion by volume). The stratospheric origin of the significantly enhanced 35S level is supported by in situ measurements of air pollutants and meteorological variables, satellite observations, meteorological analysis, and box model calculations. The deep stratospheric intrusion event was driven by the coupling between midlatitude cyclones and Santa Ana winds, and it was responsible for the regional O3 pollution episode. These results provide direct field-based evidence that 35S is an additional sensitive and unambiguous tracer in detecting stratospheric air in the boundary layer and offer the potential for resolving the stratospheric influences on the tropospheric O3 level.

  1. Detection of deep stratospheric intrusions by cosmogenic 35S.

    Science.gov (United States)

    Lin, Mang; Su, Lin; Shaheen, Robina; Fung, Jimmy C H; Thiemens, Mark H

    2016-10-04

    The extent to which stratospheric intrusions on synoptic scales influence the tropospheric ozone (O3) levels remains poorly understood, because quantitative detection of stratospheric air has been challenging. Cosmogenic (35)S mainly produced in the stratosphere has the potential to identify stratospheric air masses at ground level, but this approach has not yet been unambiguously shown. Here, we report unusually high (35)S concentrations (7,390 atoms m(-3); ∼16 times greater than annual average) in fine sulfate aerosols (aerodynamic diameter less than 0.95 µm) collected at a coastal site in southern California on May 3, 2014, when ground-level O3 mixing ratios at air quality monitoring stations across southern California (43 of 85) exceeded the recently revised US National Ambient Air Quality Standard (daily maximum 8-h average: 70 parts per billion by volume). The stratospheric origin of the significantly enhanced (35)S level is supported by in situ measurements of air pollutants and meteorological variables, satellite observations, meteorological analysis, and box model calculations. The deep stratospheric intrusion event was driven by the coupling between midlatitude cyclones and Santa Ana winds, and it was responsible for the regional O3 pollution episode. These results provide direct field-based evidence that (35)S is an additional sensitive and unambiguous tracer in detecting stratospheric air in the boundary layer and offer the potential for resolving the stratospheric influences on the tropospheric O3 level.

  2. A novel rocket-based in-situ collection technique for mesospheric and stratospheric aerosol particles

    Directory of Open Access Journals (Sweden)

    W. Reid

    2012-11-01

    Full Text Available A technique for collecting aerosol particles between altitudes of 85 and 17 km is described. Collection probes are ejected from a sounding rocket allowing for multi-point measurements. Each probe is equipped with 110 collection samples that are 3 mm in diameter. The collection samples are one of three types: standard transmission electron microscopy carbon grids, glass fibre filter paper or silicone gel. Each collection sample is exposed over a 50 m to 5 km height range with a total of 45 separate ranges. Post-flight electron microscopy gives size-resolved information on particle number, shape and elemental composition. Each collection probe is equipped with a suite of sensors to capture the probe's status during the fall. Parachute recovery systems along with GPS-based localization ensure that each probe can be located and recovered for post-flight analysis.

  3. Data pre-processing: Stratospheric aerosol perturbing effect on the remote sensing of vegetation: Correction method for the composite NDVI after the Pinatubo eruption

    Science.gov (United States)

    Vermote, E.; Elsaleous, N.; Kaufman, Y. J.; Dutton, E.

    1994-01-01

    An operational stratospheric correction scheme used after the Mount Pinatubo (Phillipines) eruption (Jun. 1991) is presented. The stratospheric aerosol distribution is assumed to be only variable with latitude. Each 9 days the latitudinal distribution of the optical thickness is computed by inverting radiances observed in the NOAA AVHRR channel 1 (0.63 micrometers) and channel 2 (0.83 micrometers) over the Pacific Ocean. This radiance data set is used to check the validity of model used for inversion by checking consistency of the optical thickness deduced from each channel as well as optical thickness deduced from different scattering angles. Using the optical thickness profile previously computed and radiative transfer code assuming Lambertian boundary condition, each pixel of channel 1 and 2 are corrected prior to computation of NDVI (Normalized Difference Vegetation Index). Comparison between corrected, non corrected, and years prior to Pinatubo eruption (1989 to 1990) NDVI composite, shows the necessity and the accuracy of the operational correction scheme.

  4. Spatial Variability of AERONET Aerosol Optical Properties and Satellite Data in South Korea during NASA DRAGON-Asia Campaign.

    Science.gov (United States)

    Lee, Hyung Joo; Son, Youn-Suk

    2016-04-05

    We investigated spatial variability in aerosol optical properties, including aerosol optical depth (AOD), fine-mode fraction (FMF), and single scattering albedo (SSA), observed at 21 Aerosol Robotic Network (AERONET) sites and satellite remote sensing data in South Korea during the spring of 2012. These dense AERONET networks established in a National Aeronautics and Space Administration (NASA) field campaign enabled us to examine the spatially detailed aerosol size distribution and composition as well as aerosol levels. The springtime particle air quality was characterized by high background aerosol levels and high contributions of coarse-mode aerosols to total aerosols. We found that between-site correlations and coefficient of divergence for AOD and FMF strongly relied on the distance between sites, particularly in the south-north direction. Higher AOD was related to higher population density and lower distance from highways, and the aerosol size distribution and composition reflected source-specific characteristics. The ratios of satellite NO2 to AOD, which indicate the relative contributions of local combustion sources to aerosol levels, represented higher local contributions in metropolitan Seoul and Pusan. Our study demonstrates that the aerosol levels were determined by both local and regional pollution and that the relative contributions of these pollutions to aerosols generated spatial heterogeneity in the particle air quality.

  5. How well can interannual to decadal-scale variability in stratospheric ozone and water vapor be quantified using limb-based satellite measurements?

    Science.gov (United States)

    Davis, S. M.; Rosenlof, K. H.; Hurst, D. F.; Hassler, B.; Read, W. G.

    2015-12-01

    Vertical profiles of ozone and humidity from the upper troposphere to stratosphere have been retrieved from a number of limb sounding and solar occultation satellite instruments since the 1980's. In particular, measurements from the SAGE instruments, UARS MLS, UARS HALOE, and most recently Aura MLS, have provided overlapping data since 1984. In order to quantify interannual- to decadal-scale variability in water vapor and ozone, it is necessary to have a uniform and homogenous record over the period of interest. With this in mind, we merged the aforementioned satellite measurements to create the Stratospheric Water and Ozone Satellite Homogenized (SWOOSH) data set, which contains vertically resolved zonal-mean (2.5°) monthly-mean water vapor and ozone concentration at levels covering the stratosphere. In this presentation, we describe the process of merging the satellite data sets, which involves adjusting the data to a reference measurement using offsets calculated from coincident observations taken during instrument overlap periods. Uncertainties associated with individual measurement precision, geophysical variability, and the merging process are quantified and compared to one another. We show that while the SWOOSH data can be used to quantify interannual variability, quantifying long-term trends in SWOOSH is complicated by the various sources of uncertainty, as well as by potential drifts of individual instruments. The issue of satellite-derived trends is discussed in relation to the long-term record of balloon-borne frostpoint hygrometer measurements from Boulder, CO.

  6. Origin of aerosol particles in the mid latitude and subtropical upper troposphere and lowermost stratosphere from cluster analysis of CARIBIC data

    Directory of Open Access Journals (Sweden)

    M. Köppe

    2009-06-01

    Full Text Available The origin of aerosol particles in the upper troposphere and lowermost stratosphere over the Eurasian continent was investigated by applying cluster analysis methods to in situ measured data. Number concentrations of submicrometer aerosol particles and trace gas mixing ratios derived by the CARIBIC (Civil Aircraft for Regular Investigation of the Atmosphere Based on an Instrument Container measurement system on flights between Germany and South-East Asia were used for this analysis. Four cluster analysis methods were applied to a test data set and their capability of separating the data points into scientifically reasonable clusters was assessed. The best method was applied to seasonal data subsets for summer and winter resulting in five cluster or air mass types: stratosphere, tropopause, free troposphere, high clouds, and boundary layer influenced. Other source clusters, like aircraft emissions could not be resolved in the present data set with the used methods. While the cluster separation works satisfactory well for the summer data, in winter interpretation is more difficult, which is attributed to either different vertical transport pathways or different chemical lifetimes in the two seasons. The geographical distribution of the clusters together with histograms for nucleation and Aitken mode particles within each cluster are presented. Aitken mode particle number concentrations show a clear vertical gradient with the lowest values in the lowermost stratosphere (750–2820 particles/cm3 STP, minimum of the two 25%- and maximum of the two 75%-percentiles of both seasons and the highest values for the boundary-layer-influenced air (4290–22 760 particles/cm3 STP. Nucleation mode particles are also highest in the boundary-layer-influenced air (1260–29 500 particles/cm3 STP, but are lowest in the free troposphere (0–450 particles/cm3 STP. The given submicrometer particle number concentrations represent the

  7. Use of satellite information for analysis of aerosol substance propagation

    Science.gov (United States)

    Lezhenin, A. A.; Raputa, V. F.; Yaroslavtseva, T. V.

    2015-11-01

    With satellite data on pollution of snow cover and data of meteorological observations, some fields of dust sedimentation from high chimneys of the Iskitim cement plant are studied. In the absence of snowfalls, a possibility to analyze of the areas of pollution, which are formed in time intervals from several days to several weeks in the vicinities of industrial enterprises, is shown.

  8. AERONET-based microphysical and optical properties of smoke-dominated aerosol near source regions and transported over oceans, and implications for satellite retrievals of aerosol optical depth

    Science.gov (United States)

    Sayer, A. M.; Hsu, N. C.; Eck, T. F.; Smirnov, A.; Holben, B. N.

    2013-09-01

    Smoke aerosols from biomass burning are an important component of the global aerosol cycle. Analysis of Aerosol Robotic Network (AERONET) retrievals of size distribution and refractive index reveals variety between biomass burning aerosols in different global source regions, in terms of aerosol particle size and single scatter albedo (SSA). Case studies of smoke transported to coastal/island AERONET sites also mostly lie within the range of variability at near-source sites. Two broad ''families'' of aerosol properties are found, corresponding to sites dominated by boreal forest burning (larger, broader fine mode, with midvisible SSA ∼0.95), and those influenced by grass, shrub, or crop burning with additional forest contributions (smaller, narrower particles with SSA ∼0.88-0.9 in the midvisible). The strongest absorption is seen in southern African savannah at Mongu (Zambia), with average SSA ∼0.85 in the midvisible. These can serve as candidate sets of aerosol microphysical/optical properties for use in satellite aerosol optical depth (AOD) retrieval algorithms. The models presently adopted by these algorithms over ocean are often insufficiently absorbing to represent these biomass burning aerosols. A corollary of this is an underestimate of AOD in smoke outflow regions, which has important consequences for applications of these satellite datasets.

  9. 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.

    Science.gov (United States)

    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.

  10. Sensitivity of high-spectral resolution and broadband thermal infrared nadir instruments to the chemical and microphysical properties of secondary sulfate aerosols in the upper-troposphere/lower-stratosphere

    Science.gov (United States)

    Sellitto, Pasquale; Legras, Bernard

    2016-04-01

    The observation of upper-tropospheric/lower-stratospheric (UTLS) secondary sulfate aerosols (SSA) and their chemical and microphysical properties from satellite nadir observations (with better spatial resolution than limb observations) is a fundamental tool to better understand their formation and evolution processes and then to estimate their impact on UTLS chemistry, and on regional and global radiative balance. Thermal infrared (TIR) observations are sensitive to the chemical composition of the aerosols due to the strong spectral variations of the imaginary part of the refractive index in this band and, correspondingly, of the absorption, as a function of the composition Then, these observations are, in principle, well adapted to detect and characterize UTLS SSA. Unfortunately, the exploitation of nadir TIR observations for sulfate aerosol layer monitoring is today very limited. Here we present a study aimed at the evaluation of the sensitivity of TIR satellite nadir observations to the chemical composition and the size distribution of idealised UTLS SSA layers. The sulfate aerosol particles are assumed as binary systems of sulfuric acid/water solution droplets, with varying sulphuric acid mixing ratios. The extinction properties of the SSA, for different sulfuric acid mixing ratios and temperatures, are systematically analysed. The extinction coefficients are derived by means of a Mie code, using refractive indices taken from the GEISA (Gestion et Étude des Informations Spectroscopiques Atmosphériques: Management and Study of Spectroscopic Information) spectroscopic database and log-normal size distributions with different effective radii and number concentrations. High-spectral resolution pseudo-observations are generated using forward radiative transfer calculations performed with the 4A (Automatized Atmospheric Absorption Atlas) radiative transfer model, to estimate the impact of the extinction of idealised aerosol layers, at typical UTLS conditions, on

  11. Stratospheric aircraft: Impact on the stratosphere

    Energy Technology Data Exchange (ETDEWEB)

    Johnston, H.

    1992-02-01

    The steady-state distribution of natural stratospheric ozone is primarily maintained through production by ultraviolet photolysis of molecular oxygen, destruction by a catalytic cycle involving nitrogen oxides (NO{sub x}), and relocation by air motions within the stratosphere. Nitrogen oxides from the exhausts of a commercially viable fleet of supersonic transports would exceed the natural source of stratospheric nitrogen oxides if the t should be equipped with 1990 technology jet engines. This model-free comparison between a vital natural global ingredient and a proposed new industrial product shows that building a large fleet of passenger stratospheric aircraft poses a significant global problem. NASA and aircraft industries have recognized this problem and are studying the redesign of jet aircraft engines in order to reduce the nitrogen oxides emissions. In 1989 atmospheric models identified two other paths by which the ozone destroying effects of stratospheric aircraft might be reduced or eliminated: (1) Use relatively low supersonic Mach numbers and flight altitudes. For a given rate of nitrogen oxides injection into the stratosphere, the calculated reduction of total ozone is a strong function of altitude, and flight altitudes well below 20 kilometers give relatively low calculated ozone reductions. (2) Include heterogeneous chemistry in the two-dimensional model calculations. Necessary conditions for answering the question on the title above are to improve the quality of our understanding of the lower stratosphere and to broaden our knowledge of hetergeneous stratospheric chemistry. This article reviews recently proposed new mechanisms for heterogeneous reactions on the global stratospheric sulfate aerosols.

  12. Stratospheric aircraft: Impact on the stratosphere?

    Energy Technology Data Exchange (ETDEWEB)

    Johnston, H.

    1992-02-01

    The steady-state distribution of natural stratospheric ozone is primarily maintained through production by ultraviolet photolysis of molecular oxygen, destruction by a catalytic cycle involving nitrogen oxides (NO{sub x}), and relocation by air motions within the stratosphere. Nitrogen oxides from the exhausts of a commercially viable fleet of supersonic transports would exceed the natural source of stratospheric nitrogen oxides if the t should be equipped with 1990 technology jet engines. This model-free comparison between a vital natural global ingredient and a proposed new industrial product shows that building a large fleet of passenger stratospheric aircraft poses a significant global problem. NASA and aircraft industries have recognized this problem and are studying the redesign of jet aircraft engines in order to reduce the nitrogen oxides emissions. In 1989 atmospheric models identified two other paths by which the ozone destroying effects of stratospheric aircraft might be reduced or eliminated: (1) Use relatively low supersonic Mach numbers and flight altitudes. For a given rate of nitrogen oxides injection into the stratosphere, the calculated reduction of total ozone is a strong function of altitude, and flight altitudes well below 20 kilometers give relatively low calculated ozone reductions. (2) Include heterogeneous chemistry in the two-dimensional model calculations. Necessary conditions for answering the question on the title above are to improve the quality of our understanding of the lower stratosphere and to broaden our knowledge of hetergeneous stratospheric chemistry. This article reviews recently proposed new mechanisms for heterogeneous reactions on the global stratospheric sulfate aerosols.

  13. Exploring the relationship between monitored ground-based and satellite aerosol measurements over the City of Johannesburg

    CSIR Research Space (South Africa)

    Garland, Rebecca M

    2012-09-01

    Full Text Available This project studied the relationship between aerosol optical depth (AOD) from the Multi-angle Imaging SpectroRadiometer (MISR) instrument on the Terra satellite, and ground-based monitored particulate matter (PM) mass concentrations measured...

  14. Condensed Acids In Antartic Stratospheric Clouds

    Science.gov (United States)

    Pueschel, R. F.; Snetsinger, K. G.; Toon, O. B.; Ferry, G. V.; Starr, W. L.; Oberbeck, V. R.; Chan, K. R.; Goodman, J. K.; Livingston, J. M.; Verma, S.; Fong, W.

    1992-01-01

    Report dicusses nitrate, sulfate, and chloride contents of stratospheric aerosols during 1987 Airborne Antarctic Ozone Experiment. Emphasizes growth of HNO3*3H2O particles in polar stratospheric clouds. Important in testing theories concerning Antarctic "ozone hole".

  15. The influence of aerosols and land-use type on NO2 satellite retrieval over China

    Science.gov (United States)

    Liu, Mengyao; Lin, Jintai; Boersma, Folkert; Eskes, Henk; Chimot, Julien

    2017-04-01

    Both aerosols and surface reflectance have a strong influence on the retrieval of NO2 tropospheric vertical column densities (VCDs), especially over China with its heavy aerosol loading and rapid changes in land-use type. However, satellite retrievals of NO2 VCDs usually do not explicitly account for aerosol optical effects and surface reflectance anisotropy (BRDF) that varies in space and time. We develop an improved algorithm to derive tropospheric AMFs and VCDs over China from the OMI instrument - POMINO and DOMINO. This method can also be applied to TropOMI NO2 retrievals in the future. With small pixels of TropOMI and higher probability of encountering clear-sky scenes, the influence of BRDF and aerosol interference becomes more important than for OMI. Daily aerosol information is taken from the GEOS-Chem chemistry transport model and the aerosol optical depth (AOD) is adjusted via MODIS AOD climatology. We take the MODIS MCD43C2 C5 product to account for BRDF effects. The relative altitude of NO2 and aerosols is critical factor influencing the NO2 retrieval. In order to evaluate the aerosol extinction profiles (AEP) of GEOS-Chem improve our algorithm, we compare the GEOS-Chem simulation with CALIOP and develop a CALIOP AEP climatology to regulate the model's AEP. This provides a new way to include aerosol information into the tracer gas retrieval for OMI and TropOMI. Preliminary results indicate that the model performs reasonably well in reproducing the AEP shape. However, it seems to overestimate aerosols under 2km and underestimate above. We find that relative humidity (RH) is an important factor influencing the AEP shape when comparing the model with observations. If we adjust the GEOS-Chem RH to CALIOP's RH, the correlations of their AEPs also improve. Besides, take advantage of our retrieval method, we executed sensitivity tests to analyze their influences on NO2 trend and spatiotemporal variations in retrieval. It' the first time to investigate

  16. The first estimates of global nucleation mode aerosol concentrations based on satellite measurements

    Directory of Open Access Journals (Sweden)

    M. Kulmala

    2011-11-01

    Full Text Available Atmospheric aerosols play a key role in the Earth's climate system by scattering and absorbing solar radiation and by acting as cloud condensation nuclei. Satellites are increasingly used to obtain information on properties of aerosol particles with a diameter larger than about 100 nm. However, new aerosol particles formed by nucleation are initially much smaller and grow into the optically active size range on time scales of many hours. In this paper we derive proxies, based on process understanding and ground-based observations, to determine the concentrations of these new particles and their spatial distribution using satellite data. The results are applied to provide seasonal variation of nucleation mode concentration. The proxies describe the concentration of nucleation mode particles over continents. The source rates are related to both regional nucleation and nucleation associated with more restricted sources. The global pattern of nucleation mode particle number concentration predicted by satellite data using our proxies is compared qualitatively against both observations and global model simulations.

  17. Extending methane profiles from aircraft into the stratosphere for satellite total column validation using the ECMWF C-IFS and TOMCAT/SLIMCAT 3-D model

    Science.gov (United States)

    Verma, Shreeya; Marshall, Julia; Parrington, Mark; Agustí-Panareda, Anna; Massart, Sebastien; Chipperfield, Martyn P.; Wilson, Christopher; Gerbig, Christoph

    2017-06-01

    Airborne observations of greenhouse gases are a very useful reference for validation of satellite-based column-averaged dry air mole fraction data. However, since the aircraft data are available only up to about 9-13 km altitude, these profiles do not fully represent the depth of the atmosphere observed by satellites and therefore need to be extended synthetically into the stratosphere. In the near future, observations of CO2 and CH4 made from passenger aircraft are expected to be available through the In-Service Aircraft for a Global Observing System (IAGOS) project. In this study, we analyse three different data sources that are available for the stratospheric extension of aircraft profiles by comparing the error introduced by each of them into the total column and provide recommendations regarding the best approach. First, we analyse CH4 fields from two different models of atmospheric composition - the European Centre for Medium-Range Weather Forecasts (ECMWF) Integrated Forecasting System for Composition (C-IFS) and the TOMCAT/SLIMCAT 3-D chemical transport model. Secondly, we consider scenarios that simulate the effect of using CH4 climatologies such as those based on balloons or satellite limb soundings. Thirdly, we assess the impact of using a priori profiles used in the satellite retrievals for the stratospheric part of the total column. We find that the models considered in this study have a better estimation of the stratospheric CH4 as compared to the climatology-based data and the satellite a priori profiles. Both the C-IFS and TOMCAT models have a bias of about -9 ppb at the locations where tropospheric vertical profiles will be measured by IAGOS. The C-IFS model, however, has a lower random error (6.5 ppb) than TOMCAT (12.8 ppb). These values are well within the minimum desired accuracy and precision of satellite total column XCH4 retrievals (10 and 34 ppb, respectively). In comparison, the a priori profile from the University of Leicester Greenhouse

  18. Aerus-GEO: newly available satellite-derived aerosol optical depth product over Europe and Africa

    Science.gov (United States)

    Carrer, D.; Roujean, J. L.; Ceamanos, X.; Six, B.; Suman, S.

    2015-12-01

    The major difficulty in detecting the aerosol signal from visible and near-infrared remote sensing observations is to reach the proper separation of the components related to the atmosphere and the surface. A method is proposed to circumvent this issue by exploiting the directional and temporal dimensions of the satellite signal through the use of a semi-empirical kernel-driven model for the surface/atmosphere coupled system. This algorithm was implemented by the ICARE Data Center (http://www.icare.univ-lille1.fr), which operationally disseminates a daily AOD product at 670 nm over the MSG disk since 2014. The proposed method referred to as AERUS-GEO (Aerosol and surface albEdo Retrieval Using a directional Splitting method - application to GEO data) is applied to three spectral bands (0.6 mm, 0.8 mm, and 1.6 mm) of MSG (Meteosat Second Generation) observations, which scan Europe, Africa, and the Eastern part of South America every 15 minutes. The daily AOD estimates at 0.63μm has been extensively validated. In contrast, the Angstrom coefficient is still going through validation and we will show the differences between the MSG derived Angstrom exponent with that of CAMS (Copernicus Atmosphere Monitoring Service) near-real time aerosol product. The impact of aerosol type on the aerosol radiative forcing will be presented as a part of future development plan.

  19. Development of a Climate Record of Tropospheric and Stratospheric Column Ozone from Satellite Remote Sensing: Evidence of an Early Recovery of Global Stratospheric Ozone

    Science.gov (United States)

    Ziemke, Jerald R.; Chandra, Sushil

    2012-01-01

    Ozone data beginning October 2004 from the Aura Ozone Monitoring Instrument (OMI) and Aura Microwave Limb Sounder (MLS) are used to evaluate the accuracy of the Cloud Slicing technique in effort to develop long data records of tropospheric and stratospheric ozone and for studying their long-term changes. Using this technique, we have produced a 32-yr (1979-2010) long record of tropospheric and stratospheric column ozone from the combined Total Ozone Mapping Spectrometer (TOMS) and OMI. Analyses of these time series suggest that the quasi-biennial oscillation (QBO) is the dominant source of inter-annual variability of stratospheric ozone and is clearest in the Southern Hemisphere during the Aura time record with related inter-annual changes of 30- 40 Dobson Units. Tropospheric ozone for the long record also indicates a QBO signal in the tropics with peak-to-peak changes varying from 2 to 7 DU. The most important result from our study is that global stratospheric ozone indicates signature of a recovery occurring with ozone abundance now approaching the levels of year 1980 and earlier. The negative trends in stratospheric ozone in both hemispheres during the first 15 yr of the record are now positive over the last 15 yr and with nearly equal magnitudes. This turnaround in stratospheric ozone loss is occurring about 20 yr earlier than predicted by many chemistry climate models. This suggests that the Montreal Protocol which was first signed in 1987 as an international agreement to reduce ozone destroying substances is working well and perhaps better than anticipated.

  20. Development of a climate record of tropospheric and stratospheric column ozone from satellite remote sensing: evidence of an early recovery of global stratospheric ozone

    Directory of Open Access Journals (Sweden)

    J. R. Ziemke

    2012-07-01

    Full Text Available Ozone data beginning October 2004 from the Aura Ozone Monitoring Instrument (OMI and Aura Microwave Limb Sounder (MLS are used to evaluate the accuracy of the Cloud Slicing technique in effort to develop long data records of tropospheric and stratospheric ozone and for studying their long-term changes. Using this technique, we have produced a 32-yr (1979–2010 long record of tropospheric and stratospheric column ozone from the combined Total Ozone Mapping Spectrometer (TOMS and OMI. Analyses of these time series suggest that the quasi-biennial oscillation (QBO is the dominant source of inter-annual variability of stratospheric ozone and is clearest in the Southern Hemisphere during the Aura time record with related inter-annual changes of 30–40 Dobson Units. Tropospheric ozone for the long record also indicates a QBO signal in the tropics with peak-to-peak changes varying from 2 to 7 DU. The most important result from our study is that global stratospheric ozone indicates signature of a recovery occurring with ozone abundance now approaching the levels of year 1980 and earlier. The negative trends in stratospheric ozone in both hemispheres during the first 15 yr of the record are now positive over the last 15 yr and with nearly equal magnitudes. This turnaround in stratospheric ozone loss is occurring about 20 yr earlier than predicted by many chemistry climate models. This suggests that the Montreal Protocol which was first signed in 1987 as an international agreement to reduce ozone destroying substances is working well and perhaps better than anticipated.

  1. Long-term temperature variations in the stratosphere and troposphere caused by changes in gas and aerosol composition of the atmosphere

    Science.gov (United States)

    Dyominov, I.; Zadorozhny, A.

    A numerical 2-D zonally averaged interactive dynamical radiative-photochemical model of the troposphere and stratosphere including aerosol physics is used for investigation of long-term temperature changes caused by anthropogenic pollution of the atmosphere by CO2 , CH4, N2O, CFCs, HCFCs, HFCs, CH 3CCl 3 and CCl4 as well as by discharges to the atmosphere of sulphate species during the Pinatubo eruption. The model allows calculating self-consistently diabatic circulation, temperature, gaseous composition of the troposphere and stratosphere at latitudes from the South to North Poles, as well as distribution of sulphate aerosol particles and polar stratospheric clouds (PSCs) of types I and II. The scenarios of expected changes of the anthropogenic pollutants for the period from 1990 through 2050 are taken from Climate Change 1995. The calculations of the long-term temperature variations due to anthropogenic emission s show that the greatest temperature changes are observed in the Southern Hemisphere in winter/spring periods. For example, the temperature changes at a height of 40 km at 45°S in December 2050 are about -4.85 K, 0.89 K, -2.21 K, and -4.32 K respectively for anthropogenic discharges of CO2, CH4, N2O, and chlorine species. The changes in the Northern Hemisphere are smaller. They are equal to about -4.5 K, 0.68 K, -1.46 K, and -3.17 K at 45°N. The temperature changes in the stratosphere are caused by the corresponding ozone variations and temperature feedbacks. In the troposphere, the temperature changes are determined by the greenhouse effect caused by optically active pollutants. For example, temperature increases near the Earth's surface at 45 °N in December of 2050 due to anthropogenic discharges of CO2, CH4, N2O, and chlorine species are about 0.87 K, 0.19 K, 0.14 K, and 0.32 K, respectively. The calculations show that short -term megaton discharges of sulphate species to the atmosphere during the Pinatubo eruption led to significant long

  2. Intercomparison of stratospheric nitrogen dioxide columns retrieved from ground-based DOAS and FTIR and satellite DOAS instruments over the subtropical Izana station

    OpenAIRE

    Robles-Gonzalez, Cristina; Navarro-Comas, Mónica; Puentedura, Olga; Schneider, Matthias; Hase, Frank; Garcia, Omaira; Blumenstock, Thomas; Gil-Ojeda, Manuel

    2016-01-01

    A 13-year analysis (2000–2012) of the NO2 vertical column densities derived from ground-based (GB) instruments and satellites has been carried out over the Izaña NDACC (Network for the Detection of the Atmospheric Composition Change) subtropical site. Ground-based DOAS (differential optical absorption spectroscopy) and FTIR (Fourier transform infrared spectroscopy) instruments are intercompared to test mutual consistency and then used for validation of stratospheric NO2 fro...

  3. Online Simulations of Global Aerosol Distributions in the NASA GEOS-4 Model and Comparisons to Satellite and Ground-Based Aerosol Optical Depth

    Science.gov (United States)

    Colarco, Peter; daSilva, Arlindo; Chin, Mian; Diehl, Thomas

    2010-01-01

    We have implemented a module for tropospheric aerosols (GO CART) online in the NASA Goddard Earth Observing System version 4 model and simulated global aerosol distributions for the period 2000-2006. The new online system offers several advantages over the previous offline version, providing a platform for aerosol data assimilation, aerosol-chemistry-climate interaction studies, and short-range chemical weather forecasting and climate prediction. We introduce as well a methodology for sampling model output consistently with satellite aerosol optical thickness (AOT) retrievals to facilitate model-satellite comparison. Our results are similar to the offline GOCART model and to the models participating in the AeroCom intercomparison. The simulated AOT has similar seasonal and regional variability and magnitude to Aerosol Robotic Network (AERONET), Moderate Resolution Imaging Spectroradiometer, and Multiangle Imaging Spectroradiometer observations. The model AOT and Angstrom parameter are consistently low relative to AERONET in biomass-burning-dominated regions, where emissions appear to be underestimated, consistent with the results of the offline GOCART model. In contrast, the model AOT is biased high in sulfate-dominated regions of North America and Europe. Our model-satellite comparison methodology shows that diurnal variability in aerosol loading is unimportant compared to sampling the model where the satellite has cloud-free observations, particularly in sulfate-dominated regions. Simulated sea salt burden and optical thickness are high by a factor of 2-3 relative to other models, and agreement between model and satellite over-ocean AOT is improved by reducing the model sea salt burden by a factor of 2. The best agreement in both AOT magnitude and variability occurs immediately downwind of the Saharan dust plume.

  4. Implementation of aerosol-cloud interactions in the regional atmosphere-aerosol model COSMO-MUSCAT(5.0) and evaluation using satellite data

    Science.gov (United States)

    Dipu, Sudhakar; Quaas, Johannes; Wolke, Ralf; Stoll, Jens; Mühlbauer, Andreas; Sourdeval, Odran; Salzmann, Marc; Heinold, Bernd; Tegen, Ina

    2017-06-01

    The regional atmospheric model Consortium for Small-scale Modeling (COSMO) coupled to the Multi-Scale Chemistry Aerosol Transport model (MUSCAT) is extended in this work to represent aerosol-cloud interactions. Previously, only one-way interactions (scavenging of aerosol and in-cloud chemistry) and aerosol-radiation interactions were included in this model. The new version allows for a microphysical aerosol effect on clouds. For this, we use the optional two-moment cloud microphysical scheme in COSMO and the online-computed aerosol information for cloud condensation nuclei concentrations (Cccn), replacing the constant Cccn profile. In the radiation scheme, we have implemented a droplet-size-dependent cloud optical depth, allowing now for aerosol-cloud-radiation interactions. To evaluate the models with satellite data, the Cloud Feedback Model Intercomparison Project Observation Simulator Package (COSP) has been implemented. A case study has been carried out to understand the effects of the modifications, where the modified modeling system is applied over the European domain with a horizontal resolution of 0.25° × 0.25°. To reduce the complexity in aerosol-cloud interactions, only warm-phase clouds are considered. We found that the online-coupled aerosol introduces significant changes for some cloud microphysical properties. The cloud effective radius shows an increase of 9.5 %, and the cloud droplet number concentration is reduced by 21.5 %.

  5. Reducing multisensor satellite monthly mean aerosol optical depth uncertainty: 1. Objective assessment of current AERONET locations

    Science.gov (United States)

    Li, Jing; Li, Xichen; Carlson, Barbara E.; Kahn, Ralph A.; Lacis, Andrew A.; Dubovik, Oleg; Nakajima, Teruyuki

    2016-11-01

    Various space-based sensors have been designed and corresponding algorithms developed to retrieve aerosol optical depth (AOD), the very basic aerosol optical property, yet considerable disagreement still exists across these different satellite data sets. Surface-based observations aim to provide ground truth for validating satellite data; hence, their deployment locations should preferably contain as much spatial information as possible, i.e., high spatial representativeness. Using a novel Ensemble Kalman Filter (EnKF)-based approach, we objectively evaluate the spatial representativeness of current Aerosol Robotic Network (AERONET) sites. Multisensor monthly mean AOD data sets from Moderate Resolution Imaging Spectroradiometer, Multiangle Imaging Spectroradiometer, Sea-viewing Wide Field-of-view Sensor, Ozone Monitoring Instrument, and Polarization and Anisotropy of Reflectances for Atmospheric Sciences coupled with Observations from a Lidar are combined into a 605-member ensemble, and AERONET data are considered as the observations to be assimilated into this ensemble using the EnKF. The assessment is made by comparing the analysis error variance (that has been constrained by ground-based measurements), with the background error variance (based on satellite data alone). Results show that the total uncertainty is reduced by 27% on average and could reach above 50% over certain places. The uncertainty reduction pattern also has distinct seasonal patterns, corresponding to the spatial distribution of seasonally varying aerosol types, such as dust in the spring for Northern Hemisphere and biomass burning in the fall for Southern Hemisphere. Dust and biomass burning sites have the highest spatial representativeness, rural and oceanic sites can also represent moderate spatial information, whereas the representativeness of urban sites is relatively localized. A spatial score ranging from 1 to 3 is assigned to each AERONET site based on the uncertainty reduction

  6. Heavy aerosol loading over the Bohai Bay as revealed by ground and satellite remote sensing

    Science.gov (United States)

    Zhang, Jinqiang; Chen, Jing; Xia, Xiangao; Che, Huizheng; Fan, Xuehua; Xie, Yiyang; Han, Zhiwei; Chen, Hongbin; Lu, Daren

    2016-01-01

    Heavy aerosol loading over the Bohai Bay, the innermost gulf of the Yellow Sea, was often recorded by the satellite observations. In order to understand aerosol optical properties and potential causes for the high aerosol loading there, a Cimel sunphotometer station (BH) was established on an offshore platform over the Bay for the first time in June 2012. The aerosol optical properties between July 2012 and July 2013 were employed to validate the satellite retrievals and to characterize temporal variability of aerosol optical properties. In particular, aerosol optical properties at BH were compared with those at Beijing (BJ), an urban station of the North China Plain (NCP), to discuss their potential difference during the same months of the same years. Mean aerosol optical depth at 550 nm (AOD) retrieved from the Moderate Resolution Imaging Spectroradiometer (MODIS) measurements over the Bohai Bay was 0.79 ± 0.68 during 2004-2013, that even exceeded value over the NCP (0.50 ± 0.57). This fact was supported by the comparison of ground-based remote sensing AODs at BH and BJ. The annual mean Cimel AOD at BH was 0.76 ± 0.62, which was larger than that at BJ (0.64 ± 0.52). The MODIS AOD difference between the Bohai Bay and the NCP was 0.29, being more than two times larger than the Cimel AOD difference between BH and BJ (0.12). This strongly implied that the MODIS retrievals had significant biases over the Bohai Bay that was likely due to sediment in the water and also sea ice in winter. A distinct seasonal variation of AOD was revealed over ocean. The maxima Cimel AOD was observed in summer (1.02 ± 0.75), which was followed by spring (0.86 ± 0.61), autumn (0.54 ± 0.41), and winter (0.39 ± 0.24); this was in good agreement with that over the NCP. High AOD over the Bohai Bay was associated with the heavy exhaust emissions from the ships across the Bay and transport of aerosols from the NCP. Furthermore, a much strong hygroscopic growth of fine mode aerosols over

  7. Clouds-Aerosols-Precipitation Satellite Analysis Tool (CAPSAT

    Directory of Open Access Journals (Sweden)

    I. M. Lensky

    2008-03-01

    Full Text Available A methodology for representing much of the physical information content of the METEOSAT Second Generation (MSG geostationary satellite using red-green-blue (RGB composites of the computed physical values of the picture elements is presented. The physical values are the solar reflectance in the solar channels and brightness temperature in the thermal channels. The main RGB compositions are (1 "Day Natural Colors", presenting vegetation in green, bare surface in brown, sea surface in black, water clouds as white, ice as magenta; (2 "Day Microphysical", presenting cloud microstructure using the solar reflectance component of the 3.9 μm, visible and thermal IR channels; (3 "Night Microphysical", also presenting clouds microstructure using the brightness temperature differences between 10.8 and 3.9 μm; (4 "Day and Night", using only thermal channels for presenting surface and cloud properties, desert dust and volcanic emissions; (5 "Air Mass", presenting mid and upper tropospheric features using thermal water vapor and ozone channels. The scientific basis for these rendering schemes is provided, with examples for the applications. The expanding use of these rendering schemes requires their proper documentation and setting as standards, which is the main objective of this publication.

  8. Dust aerosol impact on North Africa climate: a GCM investigation of aerosol-cloud-radiation interactions using A-Train satellite data

    Directory of Open Access Journals (Sweden)

    Y. Gu

    2012-02-01

    Full Text Available The climatic effects of dust aerosols in North Africa have been investigated using the atmospheric general circulation model (AGCM developed at the University of California, Los Angeles (UCLA. The model includes an efficient and physically based radiation parameterization scheme developed specifically for application to clouds and aerosols. Parameterization of the effective ice particle size in association with the aerosol first indirect effect based on ice cloud and aerosol data retrieved from A-Train satellite observations have been employed in climate model simulations. Offline simulations reveal that the direct solar, IR, and net forcings by dust aerosols at the top of the atmosphere (TOA generally increase with increasing aerosol optical depth. When the dust semi-direct effect is included with the presence of ice clouds, positive IR radiative forcing is enhanced since ice clouds trap substantial IR radiation, while the positive solar forcing with dust aerosols alone has been changed to negative values due to the strong reflection of solar radiation by clouds, indicating that cloud forcing associated with aerosol semi-direct effect could exceed direct aerosol forcing. With the aerosol first indirect effect, the net cloud forcing is generally reduced in the case for an ice water path (IWP larger than 20 g m−2. The magnitude of the reduction increases with IWP.

    AGCM simulations show that the reduced ice crystal mean effective size due to the aerosol first indirect effect results in less OLR and net solar flux at TOA over the cloudy area of the North Africa region because ice clouds with smaller size trap more IR radiation and reflect more solar radiation. The precipitation in the same area, however, increases due to the aerosol indirect effect on ice clouds, corresponding to the enhanced convection as indicated by reduced OLR. Adding the aerosol direct effect into the model simulation reduces the precipitation in the

  9. Inference of Spatiotemporal Distribution of Black Carbon Aerosols over Northern Pacific from Satellite Observations (2005-2012)

    Science.gov (United States)

    Liu, J.; Li, Z.; Mauzerall, D. L.; Fan, S.; Horowitz, L. W.; He, C.; Yi, K.; Tao, S.

    2015-12-01

    Knowledge on the spatiotemporal distribution of black carbon aerosol over the Northern Pacific is limited by a deficiency of observations. The HIAPER Pole-to-Pole Observation (HIPPO) program from 2009 to 2011 is the most comprehensive data source available and it reveals a 2 to 10 times overestimates of BC by current global models. Incorporation and assimilation of more data sources is needed to increase our understanding of the spatiotemporal distribution of black carbon aerosol and its corresponding climate effects. Based on measurements from aircraft campaigns and satellites, a robust association is observed between BC concentrations and satellite retrieved CO, tropospheric NO2, and aerosol optical depth (AOD) (R2 > 0.7). Such robust relationships indicate that BC aerosols share a similar emission sources, evolution processes and transport characteristics with other pollutants measured by satellite observations. It also establishes a basis to derive a satellite-based proxy (BC*) over remote oceans. The inferred satellite-based BC* shows that Asian export events in spring bring much more BC aerosols to the mid-Pacific than occurs in other seasons. In addition, inter-annual variability of BC* is seen over the Northern Pacific, with abundances correlated to the springtime Pacific/North American (PNA) index. The inferred BC* dataset also indicates a widespread overestimation of BC loadings by models over most remote oceans beyond the Pacific. Our method presents a novel approach to infer BC concentrations by combining satellite and aircraft observations.

  10. Multi-year satellite and surface observations of AOD in support of two-column aerosol project (TCAP) field campaign

    Science.gov (United States)

    Kassianov, Evgueni; Chand, Duli; Berg, Larry; Fast, Jerome; Tomlinson, Jason; Ferrare, Richard; Hostetler, Chris; Hair, John

    2012-11-01

    We use combined multi-year measurements from the surface and space for assessing the spatial and temporal distribution of aerosol properties within a large (~400x400 km) region centered on Cape Cod, Massachusetts, along the East Coast of the United States. The ground-based Aerosol Robotic Network (AERONET) measurements at Martha's Vineyard Coastal Observatory (MVCO) site and Moderate Resolution Imaging Spectrometer (MODIS) sensors on board the Terra and Aqua satellites provide horizontal and temporal variations of aerosol optical depth, while the Cloud- Aerosol Lidar and Infrared Pathfinder Satellite Observations (CALIPSO) offers the altitudes of aerosol-layers. The combined ground-based and satellite measurements indicated several interesting features among which were the large differences in the aerosol properties observed in July and February. We applied the climatology of aerosol properties for designing the Two-Column Aerosol Project (TCAP), which is supported by the U.S. Department of Energy's (DOE's) Atmospheric Radiation Measurement (ARM) Program. The TCAP field campaign involves 12-month deployment (started July 1, 2012) of the ground-based ARM Mobile Facility (AMF) and Mobile Aerosol Observing System (MAOS) on Cape Cod and complimentary aerosol observations from two research aircraft: the DOE Gulfstream-1 (G-1) and the National Aeronautics and Space Administration (NASA) B200 King Air. Using results from the coordinated G-1 and B200 flights during the recent (July, 2012) Intensive Observation Period, we demonstrated that the G-1 in situ measurements and B200 active remote sensing can provide complementary information on the temporal and spatial changes of the aerosol properties off the coast of North America.

  11. AERONET-based models of smoke-dominated aerosol near source regions and transported over oceans, and implications for satellite retrievals of aerosol optical depth

    Science.gov (United States)

    Sayer, A. M.; Hsu, N. C.; Eck, T. F.; Smirnov, A.; Holben, B. N.

    2014-10-01

    Smoke aerosols from biomass burning are an important component of the global aerosol system. Analysis of Aerosol Robotic Network (AERONET) retrievals of aerosol microphysical/optical parameters at 10 sites reveals variety between biomass burning aerosols in different global source regions, in terms of aerosol particle size and single scatter albedo (SSA). Case studies of smoke observed at coastal/island AERONET sites also mostly lie within the range of variability at the near-source sites. Differences between sites tend to be larger than variability at an individual site, although optical properties for some sites in different regions can be quite similar. Across the sites, typical midvisible SSA ranges from ~ 0.95-0.97 (sites dominated by boreal forest or peat burning, typically with larger fine-mode particle radius and spread) to ~ 0.88-0.9 (sites most influenced by grass, shrub, or crop burning, typically smaller fine-mode particle radius and spread). The tropical forest site Alta Floresta (Brazil) is closer to this second category, although with intermediate SSA ~ 0.92. The strongest absorption is seen in southern African savannah at Mongu (Zambia), with average midvisible SSA ~ 0.85. Sites with stronger absorption also tend to have stronger spectral gradients in SSA, becoming more absorbing at longer wavelengths. Microphysical/optical models are presented in detail so as to facilitate their use in radiative transfer calculations, including extension to UV (ultraviolet) wavelengths, and lidar ratios. One intended application is to serve as candidate optical models for use in satellite aerosol optical depth (AOD) retrieval algorithms. The models presently adopted by these algorithms over ocean often have insufficient absorption (i.e. too high SSA) to represent these biomass burning aerosols. The underestimates in satellite-retrieved AOD in smoke outflow regions, which have important consequences for applications of these satellite data sets, are consistent with

  12. Satellite assisted aerosol correlation in a sequestered CO2 leakage controlled site

    Science.gov (United States)

    Landulfo, Eduardo; da Silva Lopes, Fábio J.; Nakaema, Walter M.; de Medeiros, José A. G.; Moreira, Andrea

    2014-10-01

    Currently one of the main challenges in CO2 storage research is to grant the development, testing and validation of accurate and efficient Measuring, Monitoring and Verification (MMV) techniques to be deployed at the final storage site, targeting maximum storage efficiency at the minimal leakage risk levels. For such task a mimetic sequestration site has been deployed in Florianopolis, Brazil, in order to verify the performance of monitoring plataforms to detect and quantify leakages of ground injected CO2, namely a Cavity Ring Down System (CRDS) - Los Gatos Research - an Eddy Covariance System (Campbell Scientific and Irgason) and meteorological tower for wind, humidity, precipitation and temperature monitoring onsite. The measurement strategy for detecting CO2 leakages can be very challenging since environmental and phytogenic influence can be very severe and play a role on determining if the values measured are unambiguous or not. One external factor to be considered is the amount of incoming solar radiation which will be the driving force for the whole experimental setup and following this reasoning the amount of aerosols in the atmospheric column can be a determinant factor influencing the experimental results. Thus the investigation of measured fluxes CO2 and its concentration with the aforementioned experimental instruments and their correlation with the aerosol data should be taken into account by means of satellite borne systems dedicated to measure aerosol vertical distribution and its optical properties, in this study we have selected CALIPSO and MODIS instrumentation to help on deriving the aerosol properties and CO2 measurements.

  13. 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.

    Science.gov (United States)

    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.

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

    Science.gov (United States)

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

    2002-12-01

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

  15. Global Monitoring of Atmospheric Trace Gases, Clouds and Aerosols from UV/vis/NIR Satellite Instruments: Currents Status and Near Future Perspectives

    Science.gov (United States)

    Wagner, T.; Beirle, S.; Deutschmann, T.; Frankenberg, C.; Grzegorski, M.; Khokhar, M. F.; Kühl, S.; Marbach, T.; Mies, K.; de Vries, M. Penning; Platt, U.; Pukite, J.; Sanghavi, S.

    2008-04-01

    A new generation of UV/vis/near-IR satellite instruments like GOME (since 1995), SCIAMACHY (since 2002), OMI (since 2004), and GOME-2 (since 2006) allows to measure several important stratospheric and tropospheric trace gases like O3, NO2, OClO, HCHO, SO2, BrO, and H2O as well as clouds and aerosols from space. Because of its extended spectral range, the SCIAMACHY instrument also allows the retrieval of Greenhouse gases (CO2, CH4) and CO in the near IR. Almost all of the tropospheric trace gases are observed by these instruments for the first time. From satellite data it is possible to investigate the temporal and spatial variation. Also different sources can be characterised and quantified. The derived global distributions can serve as input and for the validation of atmospheric models. Here we give an overview on the current status of these new instruments and data products and their recent applications to various atmospheric and oceanic phenomena.

  16. Stratospheric aerosol—Observations, processes, and impact on climate

    Science.gov (United States)

    Kremser, Stefanie; Thomason, Larry W.; Hobe, Marc; Hermann, Markus; Deshler, Terry; Timmreck, Claudia; Toohey, Matthew; Stenke, Andrea; Schwarz, Joshua P.; Weigel, Ralf; Fueglistaler, Stephan; Prata, Fred J.; Vernier, Jean-Paul; Schlager, Hans; Barnes, John E.; Antuña-Marrero, Juan-Carlos; Fairlie, Duncan; Palm, Mathias; Mahieu, Emmanuel; Notholt, Justus; Rex, Markus; Bingen, Christine; Vanhellemont, Filip; Bourassa, Adam; Plane, John M. C.; Klocke, Daniel; Carn, Simon A.; Clarisse, Lieven; Trickl, Thomas; Neely, Ryan; James, Alexander D.; Rieger, Landon; Wilson, James C.; Meland, Brian

    2016-06-01

    Interest in stratospheric aerosol and its role in climate have increased over the last decade due to the observed increase in stratospheric aerosol since 2000 and the potential for changes in the sulfur cycle induced by climate change. This review provides an overview about the advances in stratospheric aerosol research since the last comprehensive assessment of stratospheric aerosol was published in 2006. A crucial development since 2006 is the substantial improvement in the agreement between in situ and space-based inferences of stratospheric aerosol properties during volcanically quiescent periods. Furthermore, new measurement systems and techniques, both in situ and space based, have been developed for measuring physical aerosol properties with greater accuracy and for characterizing aerosol composition. However, these changes induce challenges to constructing a long-term stratospheric aerosol climatology. Currently, changes in stratospheric aerosol levels less than 20% cannot be confidently quantified. The volcanic signals tend to mask any nonvolcanically driven change, making them difficult to understand. While the role of carbonyl sulfide as a substantial and relatively constant source of stratospheric sulfur has been confirmed by new observations and model simulations, large uncertainties remain with respect to the contribution from anthropogenic sulfur dioxide emissions. New evidence has been provided that stratospheric aerosol can also contain small amounts of nonsulfate matter such as black carbon and organics. Chemistry-climate models have substantially increased in quantity and sophistication. In many models the implementation of stratospheric aerosol processes is coupled to radiation and/or stratospheric chemistry modules to account for relevant feedback processes.

  17. Interpreting the cloud cover – aerosol optical depth relationship found in satellite data using a general circulation model

    Directory of Open Access Journals (Sweden)

    J. Quaas

    2010-07-01

    Full Text Available Statistical analysis of satellite data shows a positive correlation between aerosol optical depth (AOD and total cloud cover (TCC. Reasons for this relationship have been disputed in recent literature. The aim of this study is to explore how different processes contribute to one model's analog of the positive correlation between aerosol optical depth and total cloud cover seen in the satellite retrievals. We compare the slope of the linear regression between the logarithm of TCC and the logarithm of AOD, or the strength of the relationship, as derived from three satellite data sets to the ones simulated by a global aerosol-climate model. We analyse model results from two different simulations with and without a parameterisation of aerosol indirect effects, and using dry compared to humidified AOD. Perhaps not surprisingly we find that no single one of the hypotheses discussed in the literature is able to uniquely explain the positive relationship. However the dominant contribution to the model's AOD-TCC relationship can be attributed to aerosol swelling in regions where humidity is high and clouds are coincidentally found. This finding leads us to hypothesise that much of the AOD-TCC relationship seen in the satellite data is also carried by such a process, rather than the direct effects of the aerosols on the cloud fields themselves.

  18. Comparing multiple model-derived aerosol optical properties to spatially collocated ground-based and satellite measurements

    Science.gov (United States)

    Ocko, Ilissa B.; Ginoux, Paul A.

    2017-04-01

    Anthropogenic aerosols are a key factor governing Earth's climate and play a central role in human-caused climate change. However, because of aerosols' complex physical, optical, and dynamical properties, aerosols are one of the most uncertain aspects of climate modeling. Fortunately, aerosol measurement networks over the past few decades have led to the establishment of long-term observations for numerous locations worldwide. Further, the availability of datasets from several different measurement techniques (such as ground-based and satellite instruments) can help scientists increasingly improve modeling efforts. This study explores the value of evaluating several model-simulated aerosol properties with data from spatially collocated instruments. We compare aerosol optical depth (AOD; total, scattering, and absorption), single-scattering albedo (SSA), Ångström exponent (α), and extinction vertical profiles in two prominent global climate models (Geophysical Fluid Dynamics Laboratory, GFDL, CM2.1 and CM3) to seasonal observations from collocated instruments (AErosol RObotic NETwork, AERONET, and Cloud-Aerosol Lidar with Orthogonal Polarization, CALIOP) at seven polluted and biomass burning regions worldwide. We find that a multi-parameter evaluation provides key insights on model biases, data from collocated instruments can reveal underlying aerosol-governing physics, column properties wash out important vertical distinctions, and improved models does not mean all aspects are improved. We conclude that it is important to make use of all available data (parameters and instruments) when evaluating aerosol properties derived by models.

  19. Determination of the atmospheric optical depth due to the El Chichon stratospheric aerosol cloud in the polluted atmosphere of Mexico City

    Energy Technology Data Exchange (ETDEWEB)

    Galindo, Ignacio [Centro Universitario de Investigaciones en Ciencia del Ambiente, Universidad de Colima, Colima, Colima, (Mexico); Kondratyev, Kirill Ya. [Academician, Counsellor Center for Ecological Safety, Russian Academy of Sciences, St. Petersburg (Russian Federation); Zenteno, Gerardo [Instituto de Geofisica, UNAM, Mexico, D.F. (Mexico)

    1996-01-01

    Direct solar radiation measurements were used to determine the aerosol optical depth (AOD) increase associated with the presence of aerosol and large particles (ash) originating from the 28 March to 4 April 1982 El Chichon eruptions (17.5 degrees N, 93.3 degrees W; Mexico) on Mexico City's polluted atmospheric aerosol layer. The results are compared with those obtained at Vancouver, British Columbia, revealing that a first AOD increase occurred in both locations during May, June, and July 1982, the Mexico City AOD decay is more extended, not reaching normal climatological values until February 1983. Meanwhile, Vancouver's AOD reached minimum values in September 1982, which subsequently increased over a period from October 1982 to September 1983. This secondary maximum was recorded in Mexico City from March to August 1983. Results suggest that the first AOD increases in May, June and July 1982, both at Vancouver and Mexico City, are due chiefly to short life-time volcanic ash particles being located near the surface. However, the second AOD increases, associated with anomalously colored twilights, corresponds to stratospheric volcanic aerosols. [Spanish] Se utilizaron mediciones de radiacion solar directa para determinar el incremento de la profundidad optica del aerosol (AOD) asociada a la presencia de aerosoles y particulas grandes (cenizas) organizadas por las erupciones de El Chichon (17.5 grados N, 93.3 grados W; Mexico) del 28 de marzo al 4 de abril de 1982 sobre la capa atmosferica contaminada de la Ciudad de Mexico. Los resultados se comparan con los obtenidos en Vancouver, Colombia Britanica, relevando que un primer aumento de AOD ocurrio en ambos lugares durante mayo, junio y julio de 1982. Sin embargo, la AOD decayo en Ciudad de Mexico mas lentamente, alcanzando los valores climatologicos normales hasta febrero de 1983. Mientras tanto la AOD para Vancouver alcanzo valores minimos en septiembre de 1982; estos subsecuentemente se incrementaron en

  20. Complex chemical composition of colored surface films formed from reactions of propanal in sulfuric acid at upper troposphere/lower stratosphere aerosol acidities.

    Science.gov (United States)

    Van Wyngarden, A L; Pérez-Montaño, S; Bui, J V H; Li, E S W; Nelson, T E; Ha, K T; Leong, L; Iraci, L T

    Particles in the upper troposphere and lower stratosphere (UT/LS) consist mostly of concentrated sulfuric acid (40-80 wt %) in water. However, airborne measurements have shown that these particles also contain a significant fraction of organic compounds of unknown chemical composition. Acid-catalyzed reactions of carbonyl species are believed to be responsible for significant transfer of gas phase organic species into tropospheric aerosols and are potentially more important at the high acidities characteristic of UT/LS particles. In this study, experiments combining sulfuric acid (H2SO4) with propanal and with mixtures of propanal with glyoxal and/or methylglyoxal at acidities typical of UT/LS aerosols produced highly colored surface films (and solutions) that may have implications for aerosol properties. In order to identify the chemical processes responsible for the formation of the surface films, attenuated total reflectance-Fourier transform infrared (ATR-FTIR) and (1)H nuclear magnetic resonance (NMR) spectroscopies were used to analyze the chemical composition of the films. Films formed from propanal were a complex mixture of aldol condensation products, acetals and propanal itself. The major aldol condensation products were the dimer (2-methyl-2-pentenal) and 1,3,5-trimethylbenzene that was formed by cyclization of the linear aldol condensation trimer. Additionally, the strong visible absorption of the films indicates that higher-order aldol condensation products must also be present as minor species. The major acetal species were 2,4,6-triethyl-1,3,5-trioxane and longer-chain linear polyacetals which are likely to separate from the aqueous phase. Films formed on mixtures of propanal with glyoxal and/or methylglyoxal also showed evidence of products of cross-reactions. Since cross-reactions would be more likely than self-reactions under atmospheric conditions, similar reactions of aldehydes like propanal with common aerosol organic species like glyoxal and

  1. Correcting the Science Record: Direct Stratospheric Injection vs. Asian Monsoon and the Solar Escalator

    Science.gov (United States)

    Fromm, M. D.; Nedoluha, G. E.; Kablick, G. P.

    2012-12-01

    Two entries in the literature in 2012 make provocative but unsupportable claims regarding pollutant pathways from the Earth to the stratosphere. One claims the 13 June 2011 Nabro volcano (Eritrea) emitted gases and particles into the troposphere, and these constituents reached the stratosphere in great abundance via the Asian Monsoon circulation [Bourassa et al., 2012]. The other claims that smoke from the Black Saturday fire storms (Australia) was emitted into the troposphere, and was lofted ~15 km into the stratosphere by solar-induced diabatic heating [de Laat et al., 2012]. In both cases the stratospheric plumes attributed to these events spread around the globe and lasted for months. We will show that in both cases the postulated pathways are incorrect; the correct pathway is a direct convective injection by volcanic eruption and pyrocumulonimbus (pyroCb), respectively. We will present satellite data that will unambiguously reveal multiple, distinct stratospheric volcano-convection columns from Nabro connected to height-resolved volcanic SO2 and sulfate particles. In the case of Black Saturday we will characterize the pyroCb columns with ground-based radar and satellite imagery. The young pyroCb plume in the stratosphere will be characterized with a synergistic analysis of several NASA A-Train passive and active remote sensors. We will discuss the implications of our findings with respect to how satellite-based data are best used for tracking and characterizing point source injection plumes in the stratosphere. Bourassa et al. (2012), Large Volcanic Aerosol Load in the Stratosphere Linked to Asian Monsoon Transport, Science, 337, 78, DOI: 10:1126/Science.1219371 de Laat, et al. (2012), A solar escalator: Observational evidence of the self-lifting of smoke and aerosols by absorption of solar radiation in the February 2009 Australian Black Saturday plume, J. Geophys. Res., 117, D04204, doi:10.1029/2011JD017016.

  2. Analysis of long-range transport of aerosols for Portugal using 3D Chemical Transport Model and satellite measurements

    OpenAIRE

    Tchepel, Oxana; Ferreira, Joaquim; Fernandes, A.P.; Basart Alpuente, Sara; Baldasano Recio, José María; Borrego, Carlos

    2013-01-01

    The objective of this work is to assess the contribution of long-range transport of mineral dust from North Africa to the air pollution levels in Portugal based on a combination of a modelling approach and satellite observations. The Comprehensive Air Quality Model (CAMx) was applied together with the updated Dust REgional Atmospheric Model (BSC-DREAM8b) to characterise anthropogenic and natural sources of primary aerosols as well as secondary aerosols formation. The modelling results, ...

  3. Dust aerosol characterization and transport features based on combined ground-based, satellite and model-simulated data

    Science.gov (United States)

    Vijayakumar, K.; Devara, P. C. S.; Rao, S. Vijaya Bhaskara; Jayasankar, C. K.

    2016-06-01

    In this paper, we study aerosol characteristics over an urban station in Western India, during a dust event that occurred between 19 and 26 March 2012, with the help of ground-based and satellite measurements and model simulation data. The aerosol parameters are found to change significantly during dust events and they suggest dominance of coarse mode aerosols. The fine mode fraction, size distribution and single scattering albedo reveal that dust (natural) aerosols dominate the anthropogenic aerosols over the study region. Ground-based measurements show drastic reduction in visibility on the dust-laden day (22 March 2012). Additionally, HYSPLIT model and satellite daily data have been used to trace the source, path and spatial extent of dust storm events. Most of the dust aerosols, during the study period, travel from west-to-east pathway from source-to-sink region. Furthermore, aerosol vertical profiles from CALIPSO and synoptic meteorological parameters from ECMWF re-analysis data reveal a layer of thick dust extending from surface to an altitude of about 4 km, and decrease in temperature and increase in specific humidity, respectively. The aerosol radiative forcing calculations indicate more cooling at the surface and warming in the atmosphere during dust event. The results of satellite observations are found to have good consistency with ground-based air quality measurements. Synthesis of satellite data integrated with ground-based observations, supplemented by model analysis, is found to be a promising technique for improved understanding of dust storm phenomenon and its impact on regional climate.

  4. Impacts of elevated-aerosol-layer and aerosol type on the correlation of AOD and particulate matter with ground-based and satellite measurements in Nanjing, southeast China.

    Science.gov (United States)

    Han, Yong; Wu, Yonghua; Wang, Tijian; Zhuang, Bingliang; Li, Shu; Zhao, Kun

    2015-11-01

    Assessment of the correlation between aerosol optical depth (AOD) and particulate matter (PM) is critical to satellite remote sensing of air quality, e.g. ground PM10 and ground PM2.5. This study evaluates the impacts of aloft-aerosol-plume and aerosol-type on the correlation of AOD-PM by using synergistic measurement of a polarization-sensitive Raman-Mie lidar, CIMEL sunphotometer (SP) and TEOM PM samplers, as well as the satellite MODIS and CALIPSO, during April to July 2011 in Nanjing city (32.05(○)N/118.77(○)E), southeast China. Aloft-aerosol-layer and aerosol types (e.g. dust and non-dust or urban aerosol) are identified with the range-resolved polarization lidar and SP measurements. The results indicate that the correlations for AOD-PM10 and AOD-PM2.5 can be much improved when screening out the aloft-aerosol-layer. The linear regression slopes show significant differences for the dust and non-dust dominant aerosols in the planetary boundary layer (PBL). In addition, we evaluate the recent released MODIS-AOD product (Collection 6) from the "dark-target" (DT) and "deep-blue" (DB) algorithms and their correlation with the PM in Nanjing urban area. The results verify that the MODIS-DT AODs show a good correlation (R = 0.89) with the SP-AOD but with a systematic overestimate. In contrast, the MODIS-DB AOD shows a moderate correlation (R = 0.66) with the SP-AOD but with a smaller regression intercept (0.07). Furthermore, the moderately high correlations between the MODIS-AOD and PM10 (PM2.5) are indicated, which suggests the feasibility of PM estimate using the MODIS-AOD in Nanjing city.

  5. Refinements in the use of equivalent latitude for assimilating sporadic inhomogeneous stratospheric tracer observations, 1: Detecting transport of Pinatubo aerosol across a strong vortex edge

    Directory of Open Access Journals (Sweden)

    P. Good

    2004-01-01

    Full Text Available The use of PV equivalent latitude for assimilating stratospheric tracer observations is discussed - with particular regard to the errors in the equivalent latitude coordinate, and to the assimilation of sparse data. Some example measurements are assimilated: they sample the stratosphere sporadically and inhomogeneously. The aim was to obtain precise information about the isentropic tracer distribution and evolution as a function of equivalent latitude. Precision is important, if transport across barriers like the vortex edge are to be detected directly. The main challenges addressed are the errors in modelled equivalent latitude, and the non-ideal observational sampling. The methods presented allow first some assessment of equivalent latitude errors and a picture of how good or poor the observational coverage is. This information determines choices in the approach for estimating as precisely as possible the true equivalent latitude distribution of the tracer, in periods of good and poor observational coverage. This is in practice an optimisation process, since better understanding of the equivalent latitude distribution of the tracer feeds back into a clearer picture of the errors in the modelled equivalent latitude coordinate. Error estimates constrain the reliability of using equivalent latitude to make statements like 'this observation samples air poleward of the vortex edge' or that of more general model-measurement comparisons. The approach is demonstrated for ground-based lidar soundings of the Mount Pinatubo aerosol cloud, focusing on the 1991-92 arctic vortex edge between 475-520K. Equivalent latitude is estimated at the observation times and locations from Eulerian model tracers initialised with PV and forced by UK Meteorological Office analyses. With the model formulation chosen, it is shown that tracer transport of a few days resulted in an error distribution that was much closer to Gaussian form, although the mean error was not

  6. Long-term analysis of aerosol optical depth over Northeast Asia using a satellite-based measurement: MI Yonsei Aerosol Retrieval Algorithm (YAER)

    Science.gov (United States)

    Kim, Mijin; Kim, Jhoon; Yoon, Jongmin; Chung, Chu-Yong; Chung, Sung-Rae

    2017-04-01

    In 2010, the Korean geostationary earth orbit (GEO) satellite, the Communication, Ocean, and Meteorological Satellite (COMS), was launched including the Meteorological Imager (MI). The MI measures atmospheric condition over Northeast Asia (NEA) using a single visible channel centered at 0.675 μm and four IR channels at 3.75, 6.75, 10.8, 12.0 μm. The visible measurement can also be utilized for the retrieval of aerosol optical properties (AOPs). Since the GEO satellite measurement has an advantage for continuous monitoring of AOPs, we can analyze the spatiotemporal variation of the aerosol using the MI observations over NEA. Therefore, we developed an algorithm to retrieve aerosol optical depth (AOD) using the visible observation of MI, and named as MI Yonsei Aerosol Retrieval Algorithm (YAER). In this study, we investigated the accuracy of MI YAER AOD by comparing the values with the long-term products of AERONET sun-photometer. The result showed that the MI AODs were significantly overestimated than the AERONET values over bright surface in low AOD case. Because the MI visible channel centered at red color range, contribution of aerosol signal to the measured reflectance is relatively lower than the surface contribution. Therefore, the AOD error in low AOD case over bright surface can be a fundamental limitation of the algorithm. Meanwhile, an assumption of background aerosol optical depth (BAOD) could result in the retrieval uncertainty, also. To estimate the surface reflectance by considering polluted air condition over the NEA, we estimated the BAOD from the MODIS dark target (DT) aerosol products by pixel. The satellite-based AOD retrieval, however, largely depends on the accuracy of the surface reflectance estimation especially in low AOD case, and thus, the BAOD could include the uncertainty in surface reflectance estimation of the satellite-based retrieval. Therefore, we re-estimated the BAOD using the ground-based sun-photometer measurement, and

  7. Several thoughts for using new satellite remote sensing and global modeling for aerosol and cloud climate studies

    Science.gov (United States)

    Nakajima, Teruyuki; Hashimoto, Makiko; Takenaka, Hideaki; Goto, Daisuke; Oikawa, Eiji; Suzuki, Kentaroh; Uchida, Junya; Dai, Tie; Shi, Chong

    2017-04-01

    The rapid growth of satellite remote sensing technologies in the last two decades widened the utility of satellite data for understanding climate impacts of aerosols and clouds. The climate modeling community also has received the benefit of the earth observation and nowadays closed-collaboration of the two communities make us possible to challenge various applications for societal problems, such as for global warming and global-scale air pollution and others. I like to give several thoughts of new algorithm developments, model use of satellite data for climate impact studies and societal applications related with aerosols and clouds. Important issues are 1) Better aerosol detection and solar energy application using expanded observation ability of the third generation geostationary satellites, i.e. Himawari-8, GOES-R and future MTG, 2) Various observation functions by directional, polarimetric, and high resolution near-UV band by MISR, POLDER&PARASOL, GOSAT/CAI and future GOSAT2/CAI2, 3) Various applications of general purpose-imagers, MODIS, VIIRS and future GCOM-C/SGLI, and 4) Climate studies of aerosol and cloud stratification and convection with active and passive sensors, especially climate impact of BC aerosols using CLOUDSAT&CALIPSO and future Earth Explorer/EarthCARE.

  8. Characterization of aerosol pollution events in France using ground-based and POLDER-2 satellite data

    Directory of Open Access Journals (Sweden)

    M. Kacenelenbogen

    2006-01-01

    Full Text Available We analyze the relationship between daily fine particle mass concentration (PM2.5 and columnar aerosol optical thickness derived from the Polarization and Directionality of Earth's Reflectances (POLDER satellite sensor. The study is focused over France during the POLDER-2 lifetime between April and October 2003. We have first compared the POLDER derived aerosol optical thickness (AOT with integrated volume size distribution derived from ground-based Sun Photometer observations. The good correlation (R=0.72 with sub-micron volume fraction indicates that POLDER derived AOT is sensitive to the fine aerosol mass concentration. Considering 1974 match-up data points over 28 fine particle monitoring sites, the POLDER-2 derived AOT is fairly well correlated with collocated PM2.5 measurements, with a correlation coefficient of 0.55. The correlation coefficient reaches a maximum of 0.80 for particular sites. We have analyzed the probability to find an appropriate air quality category (AQC as defined by U.S. Environmental Protection Agency (EPA from POLDER-2 AOT measurements. The probability can be up to 88.8% (±3.7% for the "Good" AQC and 89.1% (±3.6% for the "Moderate" AQC.

  9. Feasibility of anomaly occurrence in aerosols time series obtained from MODIS satellite images during hazardous earthquakes

    Science.gov (United States)

    Akhoondzadeh, Mehdi; Jahani Chehrebargh, Fatemeh

    2016-09-01

    Earthquake is one of the most devastating natural disasters that its prediction has not materialized comprehensive. Remote sensing data can be used to access information which is closely related to an earthquake. The unusual variations of lithosphere, atmosphere and ionosphere parameters before the main earthquakes are considered as earthquake precursors. To date the different precursors have been proposed. This paper examines one of the parameters which can be derived from satellite imagery. The mentioned parameter is Aerosol Optical Depth (AOD) that this article reviews its relationship with earthquake. Aerosol parameter can be achieved through various methods such as AERONET ground stations or using satellite images via algorithms such as the DDV (Dark Dense Vegetation), Deep Blue Algorithm and SYNTAM (SYNergy of Terra and Aqua Modis). In this paper, by analyzing AOD's time series (derived from MODIS sensor on the TERRA platform) for 16 major earthquakes, seismic anomalies were observed before and after earthquakes. Before large earthquakes, rate of AOD increases due to the pre-seismic changes before the strong earthquake, which produces gaseous molecules and therefore AOD increases. Also because of aftershocks after the earthquake there is a significant change in AOD due to gaseous molecules and dust. These behaviors suggest that there is a close relationship between earthquakes and the unusual AOD variations. Therefore the unusual AOD variations around the time of earthquakes can be introduced as an earthquake precursor.

  10. Satellite observations of aerosol transport from East Asia to the Arctic: three case studies

    Directory of Open Access Journals (Sweden)

    M. Di Pierro

    2010-11-01

    Full Text Available Vertical profiles of aerosols obtained with the CALIOP lidar onboard CALIPSO are used in conjunction with the GEOS-Chem chemical transport model and NOAA's HYSPLIT trajectory model to document three aerosol export events from East Asia to the Arctic that occurred in the year 2007. During each of these events CALIOP sampled the pollution plumes multiple times over periods of five to seven days. Meridional transport to the Arctic was rapid, taking 3–4 days and was accompanied by net diabatic heating of ~5 °C/day and precipitation in its ascending stage. Once in the Arctic transport was nearly isentropic with slow subsidence and radiative cooling at a rate of 1–1.5 °C/day. We find close agreement between modeled and observed plume in terms of length, altitude, thickness and, within the measurement uncertainties, extinction coefficient. In one event the satellite algorithm misclassifies the aerosol layer as ice clouds as a result of the relatively high depolarization ratio (0.06, likely caused by a somewhat high dust component in the aerosol mixture. The misclassification is more severe at daytime (67% of layers are misclassified than at nighttime (32%. The two most intense export events occurred in early spring within a three-week time span and are strongly related to a persisting blocking anticyclone that was located in the NW Pacific. Using 500 hPa geopotential height anomalies of these two events along with several others in 2007–2009 we develop a meteorological index that captures 40–60% of the variance of Asian transport events to the Arctic in winter and spring.

  11. Observations of meteoric material and implications for aerosol nucleation in the winter Arctic lower stratosphere derived from in situ particle measurements

    Directory of Open Access Journals (Sweden)

    J. Curtius

    2005-01-01

    Full Text Available Number concentrations of total and non-volatile aerosol particles with size diameters >0.01 μm as well as particle size distributions (0.4–23 μm diameter were measured in situ in the Arctic lower stratosphere (10–20.5 km altitude. The measurements were obtained during the campaigns European Polar Stratospheric Cloud and Lee Wave Experiment (EUPLEX and Envisat-Arctic-Validation (EAV. The campaigns were based in Kiruna, Sweden, and took place from January to March 2003. Measurements were conducted onboard the Russian high-altitude research aircraft Geophysica using the low-pressure Condensation Nucleus Counter COPAS (COndensation PArticle Counter System and a modified FSSP 300 (Forward Scattering Spectrometer Probe. Around 18–20 km altitude typical total particle number concentrations nt range at 10–20 cm−3 (ambient conditions. Correlations with the trace gases nitrous oxide (N2O and trichlorofluoromethane (CFC-11 are discussed. Inside the polar vortex the total number of particles >0.01 μm increases with potential temperature while N2O is decreasing which indicates a source of particles in the above polar stratosphere or mesosphere. A separate channel of the COPAS instrument measures the fraction of aerosol particles non-volatile at 250°C. Inside the polar vortex a much higher fraction of particles contained non-volatile residues than outside the vortex (~67% inside vortex, ~24% outside vortex. This is most likely due to a strongly increased fraction of meteoric material in the particles which is transported downward from the mesosphere inside the polar vortex. The high fraction of non-volatile residual particles gives therefore experimental evidence for downward transport of mesospheric air inside the polar vortex. It is also shown that the fraction of non-volatile residual particles serves directly as a suitable experimental vortex tracer. Nanometer-sized meteoric smoke particles may also serve as nuclei for the condensation of

  12. CHASER: An Innovative Satellite Mission Concept to Measure the Effects of Aerosols on Clouds and Climate

    Science.gov (United States)

    Renno, N.; Williams, E.; Rosenfeld, D.; Fischer, D.; Fischer, J.; Kremic, T.; Agrawal, A.; Andreae, M.; Bierbaum, R.; Blakeslee, R.; Boerner, A.; Bowles, N.; Christian, H.; Dunion, J.; Horvath, A.; Huang, X.; Khain, A.; Kinne, S.; Lemos, M.-C.; Penner, J.

    2012-04-01

    The formation of cloud droplets on aerosol particles, technically known as the activation of cloud condensation nuclei (CCN), is the fundamental process driving the interactions of aerosols with clouds and precipitation. Knowledge of these interactions is foundational to our understanding of weather and climate. The Intergovernmental Panel on Climate Change (IPCC) and the Decadal Survey (NRC 2007) indicate that the uncertainty in how clouds adjust to aerosol perturbations dominates the uncertainty in the overall quantification of the radiative forcing attributable to human activities. The Clouds, Hazards, and Aerosols Survey for Earth Researchers (CHASER) mission concept responds to the IPCC and Decadal Survey concerns by studying the activation of CCN and their interactions with clouds and storms. CHASER proposes to revolutionize our understanding of the interactions of aerosols with clouds by making the first global measurements of the fundamental physical entity linking them: activated cloud condensation nuclei. The CHASER mission was conceptualized to measure all quantities necessary for determining the interactions of aerosols with clouds and storms. Measurements by current satellites allow the determination of crude profiles of cloud particle size but not of the activated CCN that seed them. CHASER uses a new technique (Freud et al. 2011; Rosenfeld et al. 2012) and high-heritage instruments to produce the first global maps of activated CCN and the properties of the clouds associated with them. CHASER measures the CCN concentration and cloud thermodynamic forcing simultaneously, allowing their effects to be distinguished. Changes in the behavior of a group of weather systems in which only one of the quantities varies (a partial derivative of the intensity with the desirable quantity) allow the determination of each effect statistically. The high uncertainties of current climate predictions limit their much-needed use in decision-making. CHASER mitigates this

  13. Global volcanic aerosol properties derived from emissions, 1990-2014, using CESM1(WACCM): VOLCANIC AEROSOLS DERIVED FROM EMISSIONS

    Energy Technology Data Exchange (ETDEWEB)

    Mills, Michael J. [Atmospheric Chemistry Observations and Modeling Laboratory, National Center for Atmospheric Research, Boulder Colorado USA; Schmidt, Anja [School of Earth and Environment, University of Leeds, Leeds UK; Easter, Richard [Atmospheric Sciences and Global Change Division, Pacific Northwest National Laboratory, Richland Washington USA; Solomon, Susan [Department of Earth, Atmospheric, and Planetary Sciences, Massachusetts Institute of Technology, Cambridge Massachusetts USA; Kinnison, Douglas E. [Atmospheric Chemistry Observations and Modeling Laboratory, National Center for Atmospheric Research, Boulder Colorado USA; Ghan, Steven J. [Atmospheric Sciences and Global Change Division, Pacific Northwest National Laboratory, Richland Washington USA; Neely, Ryan R. [School of Earth and Environment, University of Leeds, Leeds UK; National Centre for Atmospheric Science, University of Leeds, Leeds UK; Marsh, Daniel R. [Atmospheric Chemistry Observations and Modeling Laboratory, National Center for Atmospheric Research, Boulder Colorado USA; Conley, Andrew [Atmospheric Chemistry Observations and Modeling Laboratory, National Center for Atmospheric Research, Boulder Colorado USA; Bardeen, Charles G. [Atmospheric Chemistry Observations and Modeling Laboratory, National Center for Atmospheric Research, Boulder Colorado USA; Gettelman, Andrew [Atmospheric Chemistry Observations and Modeling Laboratory, National Center for Atmospheric Research, Boulder Colorado USA

    2016-03-06

    Accurate representation of global stratospheric aerosol properties from volcanic and non-volcanic sulfur emissions is key to understanding the cooling effects and ozone-loss enhancements of recent volcanic activity. Attribution of climate and ozone variability to volcanic activity is of particular interest in relation to the post-2000 slowing in the apparent rate of global average temperature increases, and variable recovery of the Antarctic ozone hole. We have developed a climatology of global aerosol properties from 1990 to 2014 calculated based on volcanic and non-volcanic emissions of sulfur sources. We have complied a database of volcanic SO2 emissions and plume altitudes for eruptions between 1990 and 2014, and a new prognostic capability for simulating stratospheric sulfate aerosols in version 5 of the Whole Atmosphere Community Climate Model, a component of the Community Earth System Model. Our climatology shows remarkable agreement with ground-based lidar observations of stratospheric aerosol optical depth (SAOD), and with in situ measurements of aerosol surface area density (SAD). These properties are key parameters in calculating the radiative and chemical effects of stratospheric aerosols. Our SAOD climatology represents a significant improvement over satellite-based analyses, which 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 climatology significantly improves on that provided for the Chemistry-Climate Model Initiative, which misses 60% of the SAD measured in situ. Our climatology of aerosol properties is publicly available on the Earth System Grid.

  14. QUantifying the Aerosol Direct and Indirect Effect over Eastern Mediterranean from Satellites (QUADIEEMS): Overview and preliminary results

    Science.gov (United States)

    Georgoulias, Aristeidis K.; Zanis, Prodromos; Pöschl, Ulrich; Kourtidis, Konstantinos A.; Alexandri, Georgia; Ntogras, Christos; Marinou, Eleni; Amiridis, Vassilis

    2013-04-01

    An overview and preliminary results from the research implemented within the framework of QUADIEEMS project are presented. For the scopes of the project, satellite data from five sensors (MODIS aboard EOS TERRA, MODIS aboard EOS AQUA, TOMS aboard Earth Probe, OMI aboard EOS AURA and CALIOP aboard CALIPSO) are used in conjunction with meteorological data from ECMWF ERA-interim reanalysis and data from a global chemical-aerosol-transport model as well as simulation results from a regional climate model (RegCM4) coupled with a simplified aerosol scheme. QUADIEEMS focuses on Eastern Mediterranean [30oN-45No, 17.5oE-37.5oE], a region situated at the crossroad of different aerosol types and thus ideal for the investigation of the direct and indirect effects of various aerosol types at a high spatial resolution. The project consists of five components. First, raw data from various databases are acquired, analyzed and spatially homogenized with the outcome being a high resolution (0.1x0.1 degree) and a moderate resolution (1.0x1.0 degree) gridded dataset of aerosol and cloud optical properties. The marine, dust and anthropogenic fraction of aerosols over the region is quantified making use of the homogenized dataset. Regional climate model simulations with REGCM4/aerosol are also implemented for the greater European region for the period 2000-2010 at a resolution of 50 km. REGCM4's ability to simulate AOD550 over Europe is evaluated. The aerosol-cloud relationships, for sub-regions of Eastern Mediterranean characterized by the presence of predominant aerosol types, are examined. The aerosol-cloud relationships are also examined taking into account the relative position of aerosol and cloud layers as defined by CALIPSO observations. Within the final component of the project, results and data that emerged from all the previous components are used in satellite-based parameterizations in order to quantify the direct and indirect (first) radiative effect of the different

  15. Volcanic aerosols: Chemistry, evolution, and effects

    Science.gov (United States)

    Turco, Richard

    1991-01-01

    Stratospheric aerosols have been the subject of scientific speculation since the 1880s, when the powerful eruption of Krakatoa attracted worldwide attention to the upper atmosphere through spectacular optical displays. The presence of a permanent tenuous dust layer in the lower stratosphere was postulated in the 1920s following studies of the twilight glow. Junge collected the first samples of these 'dust' particles and demonstrated that they were actually composed of sulfates, most likely concentrated sulfuric acid (Junge and Manson, 1961; Junge, 1963). Subsequent research has been spurred by the realization that stratospheric particles can influence the surface climate of earth through their effects on atmospheric radiation. Such aerosols can also influence, through chemical and physical effects, the trace composition of the atmosphere, ozone concentrations, and atmospheric electrical properties. The properties of stratospheric aerosols (both the background particles and those enhanced by volcanic eruptions) were measured in situ by balloon ascents and high altitude aircraft sorties. The aerosols were also observed remotely from the ground and from satellites using both active (lidar) and passive (solar occultation) techniques (remote sensing instruments were carried on aircraft and balloon platforms as well). In connection with the experimental work, models were developed to test theories of particle formation and evolution, to guide measurement strategies, to provide a means of connecting laboratory and field data, and to apply the knowledge gained to answer practical questions about global changes in climate, depletion of the ozone layer, and related environmental problems.

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

    Science.gov (United States)

    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.

  17. Global top-down smoke aerosol emissions estimation using satellite fire radiative power measurements

    Directory of Open Access Journals (Sweden)

    C. Ichoku

    2013-10-01

    Full Text Available Biomass burning occurs seasonally in most vegetated parts of the world, consuming large amounts of biomass fuel, generating intense heat energy, and emitting corresponding amounts of smoke plumes that comprise different species of aerosols and trace gases. Accurate estimates of these emissions are required as model inputs to evaluate and forecast smoke plume transport and impacts on air quality, human health, clouds, weather, radiation, and climate. Emissions estimates have long been based on bottom-up approaches that are not only complex, but also fraught with compounding uncertainties. Fortunately, a series of recent studies have revealed that both the rate of biomass consumption and the rate of emission of aerosol particulate matter (PM by open biomass burning are directly proportional to the rate of release of fire radiative energy (FRE, which is fire radiative power (FRP that is measurable from satellite. This direct relationship enables the determination of coefficients of emission (Ce, which can be used to convert FRP or FRE to smoke aerosol emissions in the same manner as emission factors (EFs are used to convert burned biomass to emissions. We have leveraged this relationship to generate the first global 1° × 1° gridded Ce product for smoke aerosol or total particulate matter (TPM emissions using coincident measurements of FRP and aerosol optical thickness (AOT from the Moderate-resolution Imaging Spectro-radiometer (MODIS sensors aboard the Terra and Aqua satellites. This new Fire Energetics and Emissions Research version 1.0 (FEER.v1 Ce product has now been released to the community and can be obtained from http://feer.gsfc.nasa.gov/, along with the corresponding 1-to-1 mapping of their quality assurance (QA flags that will enable the Ce values to be filtered by quality for use in various applications. The regional averages of Ce values for different ecosystem types were found to be in the ranges of: 16–21 g MJ−1 for savanna

  18. Estimating Ground-Level Particulate Matter (PM) Concentration using Satellite-derived Aerosol Optical Depth (AOD)

    Science.gov (United States)

    Park, Seohui; Im, Jungho

    2017-04-01

    Atmospheric aerosols are strongly associated with adverse human health effects. In particular, particulate matter less than 10 micrometers and 2.5 micrometers (i.e., PM10 and PM2.5, respectively) can cause cardiovascular and lung diseases such as asthma and chronic obstructive pulmonary disease (COPD). Air quality including PM has typically been monitored using station-based in-situ measurements over the world. However, in situ measurements do not provide spatial continuity over large areas. An alternative approach is to use satellite remote sensing as it provides data over vast areas at high temporal resolution. The literature shows that PM concentrations are related with Aerosol Optical Depth (AOD) that is derived from satellite observations, but it is still difficult to identify PM concentrations directly from AOD. Some studies used statistical approaches for estimating PM concentrations from AOD while some others combined numerical models and satellite-derived AOD. In this study, satellite-derived products were used to estimate ground PM concentrations based on machine learning over South Korea. Satellite-derived products include AOD from Geostationary Ocean Color Imager (GOCI), precipitation from Tropical Rainfall Measuring Mission (TRMM), soil moisture from AMSR-2, elevation from Shuttle Radar Topography Mission (SRTM), and land cover, land surface temperature and normalized difference vegetation index (NDVI) from Moderate Resolution Imaging Spectroradiometer (MODIS). PM concentrations data were collected from 318 stations. A statistical ordinary least squares (OLS) approach was also tested and compared with the machine learning approach (i.e., random forest). PM concentration was estimated during spring season (from March to May) in 2015 that typically shows high concentration of PM. The randomly selected 80% of data were used for model calibration and the remaining 20% were used for validation. The developed models were further tested for prediction of PM

  19. Dust aerosol impact on North Africa climate: a GCM investigation of aerosol-cloud-radiation interactions using A-Train satellite data

    Directory of Open Access Journals (Sweden)

    Y. Gu

    2011-12-01

    Full Text Available The climatic effects of dust aerosols in North Africa have been investigated using the atmospheric general circulation model (AGCM developed at the University of California, Los Angeles (UCLA. The model includes an efficient and physically based radiation parameterization scheme developed specifically for application to clouds and aerosols. Parameterization of the effective ice particle size in association with the aerosol first indirect effect based on ice cloud and aerosol data retrieved from A-Train satellite observations have been employed in climate model simulations. Offline simulations reveal that the direct solar, IR, and net forcings by dust aerosols at the top of the atmosphere (TOA generally increase with increasing aerosol optical depth (AOD. When the dust semi-direct effect is included with the presence of ice clouds, positive IR radiative forcing is enhanced since ice clouds trap substantial IR radiation, while the positive solar forcing with dust aerosols alone has been changed to negative values due to the strong reflection of solar radiation by clouds, indicating that cloud forcing associated with aerosol semi-direct effect could exceed direct aerosol forcing. With the aerosol first indirect effect, the net cloud forcing is generally reduced for an ice water path (IWP larger than 20 g m−2. The magnitude of the reduction increases with IWP.

    AGCM simulations show that the reduced ice crystal mean effective size due to the aerosol first indirect effect results in less OLR and net solar flux at the top of the atmosphere over the cloudy area of the North Africa region because ice clouds with smaller size trap more IR radiation and reflect more solar radiation. The precipitation in the same area, however, increases due to the aerosol indirect effect on ice clouds, corresponding to the enhanced convection as indicated by reduced OLR. The increased precipitation appears to be associated with enhanced ice water

  20. Satellite observations of middle atmosphere gravity wave absolute momentum flux and of its vertical gradient during recent stratospheric warmings

    Science.gov (United States)

    Ern, Manfred; Trinh, Quang Thai; Kaufmann, Martin; Krisch, Isabell; Preusse, Peter; Ungermann, Jörn; Zhu, Yajun; Gille, John C.; Mlynczak, Martin G.; Russell, James M., III; Schwartz, Michael J.; Riese, Martin

    2016-08-01

    Sudden stratospheric warmings (SSWs) are circulation anomalies in the polar region during winter. They mostly occur in the Northern Hemisphere and affect also surface weather and climate. Both planetary waves and gravity waves contribute to the onset and evolution of SSWs. While the role of planetary waves for SSW evolution has been recognized, the effect of gravity waves is still not fully understood, and has not been comprehensively analyzed based on global observations. In particular, information on the gravity wave driving of the background winds during SSWs is still missing.We investigate the boreal winters from 2001/2002 until 2013/2014. Absolute gravity wave momentum fluxes and gravity wave dissipation (potential drag) are estimated from temperature observations of the satellite instruments HIRDLS and SABER. In agreement with previous work, we find that sometimes gravity wave activity is enhanced before or around the central date of major SSWs, particularly during vortex-split events. Often, SSWs are associated with polar-night jet oscillation (PJO) events. For these events, we find that gravity wave activity is strongly suppressed when the wind has reversed from eastward to westward (usually after the central date of a major SSW). In addition, gravity wave potential drag at the bottom of the newly forming eastward-directed jet is remarkably weak, while considerable potential drag at the top of the jet likely contributes to the downward propagation of both the jet and the new elevated stratopause. During PJO events, we also find some indication for poleward propagation of gravity waves. Another striking finding is that obviously localized gravity wave sources, likely mountain waves and jet-generated gravity waves, play an important role during the evolution of SSWs and potentially contribute to the triggering of SSWs by preconditioning the shape of the polar vortex. The distribution of these hot spots is highly variable and strongly depends on the zonal and

  1. Intercomparison between CMIP5 model and MODIS satellite-retrieved data of aerosol optical depth, cloud fraction, and cloud-aerosol interactions

    Science.gov (United States)

    Sockol, Alyssa; Small Griswold, Jennifer D.

    2017-08-01

    Aerosols are a critical component of the Earth's atmosphere and can affect the climate of the Earth through their interactions with solar radiation and clouds. Cloud fraction (CF) and aerosol optical depth (AOD) at 550 nm from the Moderate Resolution Imaging Spectroradiometer (MODIS) are used with analogous cloud and aerosol properties from Historical Phase 5 of the Coupled Model Intercomparison Project (CMIP5) model runs that explicitly include anthropogenic aerosols and parameterized cloud-aerosol interactions. The models underestimate AOD by approximately 15% and underestimate CF by approximately 10% overall on a global scale. A regional analysis is then used to evaluate model performance in two regions with known biomass burning activity and absorbing aerosol (South America (SAM) and South Africa (SAF)). In SAM, the models overestimate AOD by 4.8% and underestimate CF by 14%. In SAF, the models underestimate AOD by 35% and overestimate CF by 13.4%. Average annual cycles show that the monthly timing of AOD peaks closely match satellite data in both SAM and SAF for all except the Community Atmosphere Model 5 and Geophysical Fluid Dynamics Laboratory (GFDL) models. Monthly timing of CF peaks closely match for all models (except GFDL) for SAM and SAF. Sorting monthly averaged 2° × 2.5° model or MODIS CF as a function of AOD does not result in the previously observed "boomerang"-shaped CF versus AOD relationship characteristic of regions with absorbing aerosols from biomass burning. Cloud-aerosol interactions, as observed using daily (or higher) temporal resolution data, are not reproducible at the spatial or temporal resolution provided by the CMIP5 models.

  2. Inversion of Aerosol Optical Depth Based on the CCD and IRS Sensors on the HJ-1 Satellites

    Directory of Open Access Journals (Sweden)

    Yang Zhang

    2014-09-01

    Full Text Available To perform a high-resolution aerosol optical depth (AOD inversion from the HJ-1 satellites, a dark pixel algorithm utilizing the HJ-1 satellite data was developed based on the Moderate-Resolution Imaging Spectroradiometer (MODIS algorithm. By analyzing the relationship between the apparent reflectance from the 1.65 μm and 2.1 μm channels of MODIS, a method for estimating albedo using the 1.65 μm channel data of the HJ-1 satellites was established, and a high-resolution AOD inversion in the Chengdu region based on the HJ-1 satellite was completed. A comparison of the inversion results with CE318 measured data produced a correlation of 0.957, respectively, with an absolute error of 0.106. An analysis of the AOD inversion results from different aerosol models showed that the rural aerosol model was suitable as a general model for establishing an aerosol inversion look-up table for the Chengdu region.

  3. Absorption Properties of Mediterranean Aerosols Obtained from Multi-year Ground-based and Satellite Remote Sensing Observations

    Science.gov (United States)

    Mallet, M.; Dubovik, O.; Nabat, P.; Dulac, F.; Kahn, R.; Sciare, J.; Paronis, D.; Leon, J. F.

    2013-01-01

    Aerosol absorption properties are of high importance to assess aerosol impact on regional climate. This study presents an analysis of aerosol absorption products obtained over the Mediterranean Basin or land stations in the region from multi-year ground-based AERONET and satellite observations with a focus on the Absorbing Aerosol Optical Depth (AAOD), Single Scattering Albedo (SSA) and their spectral dependence. The AAOD and Absorption Angstrom Exponent (AAE) data set is composed of daily averaged AERONET level 2 data from a total of 22 Mediterranean stations having long time series, mainly under the influence of urban-industrial aerosols and/or soil dust. This data set covers the 17 yr period 1996-2012 with most data being from 2003-2011 (approximately 89 percent of level-2 AAOD data). Since AERONET level-2 absorption products require a high aerosol load (AOD at 440 nm greater than 0.4), which is most often related to the presence of desert dust, we also consider level-1.5 SSA data, despite their higher uncertainty, and filter out data with an Angstrom exponent less than 1.0 in order to study absorption by carbonaceous aerosols. The SSA data set includes both AERONET level-2 and satellite level-3 products. Satellite-derived SSA data considered are monthly level 3 products mapped at the regional scale for the spring and summer seasons that exhibit the largest aerosol loads. The satellite SSA dataset includes the following products: (i) Multi-angle Imaging SpectroRadiometer (MISR) over 2000-2011, (ii) Ozone Monitoring Instrument (OMI) near-UV algorithm over 2004-2010, and (iii) MODerate resolution Imaging Spectroradiometer (MODIS) Deep-Blue algorithm over 2005-2011, derived only over land in dusty conditions. Sun-photometer observations show that values of AAOD at 440 nm vary between 0.024 +/- 0.01 (resp. 0.040 +/- 0.01) and 0.050 +/- 0.01 (0.055 +/- 0.01) for urban (dusty) sites. Analysis shows that the Mediterranean urban-industrial aerosols appear "moderately

  4. How stratospheric are deep stratospheric intrusions?

    Science.gov (United States)

    Trickl, T.; Vogelmann, H.; Giehl, H.; Scheel, H.-E.; Sprenger, M.; Stohl, A.

    2014-09-01

    Preliminary attempts of quantifying the stratospheric ozone contribution in the observations at the Zugspitze summit (2962 m a.s.l.) next to Garmisch-Partenkirchen in the German Alps had yielded an approximate doubling of the stratospheric fraction of the Zugspitze ozone during the time period 1978 to 2004. These investigations had been based on data filtering by using low relative humidity (RH) and elevated 7Be as the criteria for selecting half-hour intervals of ozone data representative of stratospheric intrusion air. To quantify the residual stratospheric component in stratospherically influenced air masses, however, the mixing of tropospheric air into the stratospheric intrusion layers must be taken into account. In fact, the dewpoint mirror instrument at the Zugspitze summit station rarely registers RH values lower than 10% in stratospheric air intrusions. Since 2007 a programme of routine lidar sounding of ozone, water vapour and aerosol has been conducted in the Garmisch-Partenkirchen area. The lidar results demonstrate that the intrusion layers are drier by roughly one order of magnitude than indicated in the in situ measurements. Even in thin layers RH values clearly below 1% have frequently been observed. These thin, undiluted layers present an important challenge for atmospheric modelling. Although the ozone values never reach values typical of the lower-stratosphere it becomes, thus, obvious that, without strong wind shear or convective processes, mixing of stratospheric and tropospheric air must be very slow in most of the free troposphere. As a consequence, the analysis the Zugspitze data can be assumed to be more reliable than anticipated. Finally, the concentrations of Zugspitze carbon monoxide rarely drop inside intrusion layers and normally stay clearly above full stratospheric values. This indicates that most of the CO, and thus the intrusion air mass, originates in the shallow "mixing layer" around the thermal tropopause. The CO mixing ratio in

  5. How stratospheric are deep stratospheric intrusions?

    Directory of Open Access Journals (Sweden)

    T. Trickl

    2014-06-01

    Full Text Available Preliminary attempts of quantifying the stratospheric ozone contribution in the observations at the Zugspitze summit (2962 m a.s.l. next to Garmisch-Partenkirchen in the German Alps had yielded an approximate doubling of the stratospheric fraction of the Zugspitze ozone during the time period 1978 and 2004. These investigations had been based on data filtering by using low relative humidity and elevated 7Be as the criteria for selecting half-hour intervals of ozone data representative of stratospheric intrusion air. For quantifying the residual stratospheric component in stratospherically influenced air masses, however, the mixing of tropospheric air into the stratospheric intrusion layers must be taken into account. In fact, the dew-point-mirror instrument at the Zugspitze summit station rarely registers relative humidity (RH values lower than 10% in stratospheric air intrusions. Since 2007 a programme of routine lidar sounding of ozone, water vapour and aerosol has been conducted in the Garmisch-Partenkirchen area. The lidar results demonstrate that the intrusion layers are dryer by roughly one order of magnitude than indicated in the in-situ measurements. Even in thin layers frequently RH values clearly below 1% have been observed. These thin, undiluted layers present an important challenge for atmospheric modelling. Although the ozone values never reach values typical of the lower-stratosphere it becomes, thus, obvious that, without strong wind shear or convective processes, mixing of stratospheric and tropospheric air must be very slow in most of the free troposphere. As a consequence, the analysis the Zugspitze data can be assumed to be more reliable than anticipated. Finally, the concentrations of Zugspitze carbon monoxide rarely drop inside intrusion layers and normally stay clearly above full stratospheric values. This indicates that most of the CO and, thus, the intrusion air mass originate in the shallow "mixing layer" around the

  6. How stratospheric are deep stratospheric intrusions?

    Directory of Open Access Journals (Sweden)

    T. Trickl

    2014-09-01

    Full Text Available Preliminary attempts of quantifying the stratospheric ozone contribution in the observations at the Zugspitze summit (2962 m a.s.l. next to Garmisch-Partenkirchen in the German Alps had yielded an approximate doubling of the stratospheric fraction of the Zugspitze ozone during the time period 1978 to 2004. These investigations had been based on data filtering by using low relative humidity (RH and elevated 7Be as the criteria for selecting half-hour intervals of ozone data representative of stratospheric intrusion air. To quantify the residual stratospheric component in stratospherically influenced air masses, however, the mixing of tropospheric air into the stratospheric intrusion layers must be taken into account. In fact, the dewpoint mirror instrument at the Zugspitze summit station rarely registers RH values lower than 10% in stratospheric air intrusions. Since 2007 a programme of routine lidar sounding of ozone, water vapour and aerosol has been conducted in the Garmisch-Partenkirchen area. The lidar results demonstrate that the intrusion layers are drier by roughly one order of magnitude than indicated in the in situ measurements. Even in thin layers RH values clearly below 1% have frequently been observed. These thin, undiluted layers present an important challenge for atmospheric modelling. Although the ozone values never reach values typical of the lower-stratosphere it becomes, thus, obvious that, without strong wind shear or convective processes, mixing of stratospheric and tropospheric air must be very slow in most of the free troposphere. As a consequence, the analysis the Zugspitze data can be assumed to be more reliable than anticipated. Finally, the concentrations of Zugspitze carbon monoxide rarely drop inside intrusion layers and normally stay clearly above full stratospheric values. This indicates that most of the CO, and thus the intrusion air mass, originates in the shallow "mixing layer" around the thermal tropopause. The

  7. Inter-comparison of model-simulated and satellite-retrieved componential aerosol optical depths in China

    Science.gov (United States)

    Li, Shenshen; Yu, Chao; Chen, Liangfu; Tao, Jinhua; Letu, Husi; Ge, Wei; Si, Yidan; Liu, Yang

    2016-09-01

    China's large aerosol emissions have major impacts on global climate change as well as regional air pollution and its associated disease burdens. A detailed understanding of the spatiotemporal patterns of aerosol components is necessary for the calculation of aerosol radiative forcing and the development of effective emission control policy. Model-simulated and satellite-retrieved aerosol components can support climate change research, PM2.5 source appointment and epidemiological studies. This study evaluated the total and componential aerosol optical depth (AOD) from the GEOS-Chem model (GC) and the Global Ozone Chemistry Aerosol Radiation and Transport model (GOCART), and the Multiangle Imaging Spectroradiometer (MISR) from 2006 to 2009 in China. Linear regression analysis between the GC and AErosol RObotic NETwork (AERONET) in China yielded similar correlation coefficients (0.6 daily, 0.71 monthly) but lower slopes (0.41 daily, 0.58 monthly) compared with those in the U.S. This difference was attributed to GC's underestimation of water-soluble AOD (WAOD) west of the Heihe-Tengchong Line, the dust AOD (DAOD) in the fall and winter, and the soot AOD (SAOD) throughout the year and throughout the country. GOCART exhibits the strongest dust estimation capability among all datasets. However, the GOCART soot distribution in the Northeast and Southeast has significant errors, and its WAOD in the polluted North China Plain (NCP) and the South is underestimated. MISR significantly overestimates the water-soluble aerosol levels in the West, and does not capture the high dust loadings in all seasons and regions, and the SAOD in the NCP. These discrepancies can mainly be attributed to the uncertainties in the emission inventories of both models, the poor performance of GC under China's high aerosol loading conditions, the omission of certain aerosol tracers in GOCART, and the tendency of MISR to misidentify dust and non-dust mixtures.

  8. Determination of the total grain size distribution in a vulcanian eruption column, and its implications to stratospheric aerosol perturbation

    Science.gov (United States)

    Murrow, P. J.; Rose, W. I., Jr.; Self, S.

    1980-11-01

    The total grain distribution of tephra from the eruption by the Fuego volcano in Guatemala on Oct. 14, 1974 was determined by grain size analysis. The region within each isopach has a grain distribution which was weighted proportionally to its percentage volume; the total distribution had a median grain size of 0.6 mm and a sorting coefficient of 2.3. The ash composed of fine particles did not fall in the volcano area as part of the recognizable tephra blanket; the eruption column reached well into the stratosphere to the height of 10-12 km above sea level, with mass flux rate estimated altitudes of 18-23 km

  9. Stratospheric ClO and ozone from the Microwave Limb Sounder on the Upper Atmosphere Research Satellite

    Science.gov (United States)

    Waters, J. W.; Froidevaux, L.; Read, W. G.; Manney, G. L.; Elson, L. S.; Flower, D. A.; Jarnot, R. F.; Harwood, R. S.

    1993-01-01

    Concentrations of atmospheric ozone and of ClO (the predominant form of reactive chlorine responsible for stratospheric ozone depletion) are reported for both the Arctic and Antarctic winters of the past 18 months. Chlorine in the lower stratosphere was almost completely converted to chemically reactive forms in both the northern and southern polar winter vortices. This occurred in the south long before the development of the Antarctic ozone hole, suggesting that ozone loss can be masked by influx of ozone-rich air.

  10. An offline constrained data assimilation technique for aerosols: Improving GCM simulations over South Asia using observations from two satellite sensors

    Science.gov (United States)

    Baraskar, Ankit; Bhushan, Mani; Venkataraman, Chandra; Cherian, Ribu

    2016-05-01

    Aerosol properties simulated by general circulation models (GCMs) exhibit large uncertainties due to biases in model processes and inaccuracies in aerosol emission inputs. In this work, we propose an offline, constrained optimization based procedure to improve these simulations by assimilating them with observational data. The proposed approach explicitly incorporates the non-negativity constraint on the aerosol optical depth (AOD) which is a key metric to quantify aerosol distributions. The resulting optimization problem is quadratic programming in nature and can be easily solved by available optimization routines. The utility of the approach is demonstrated by performing offline assimilation of GCM simulated aerosol optical properties and radiative forcing over South Asia (40-120 E, 5-40 N), with satellite AOD measurements from two sensors, namely Moderate Resolution Imaging SpectroRadiometer (MODIS) and Multi-Angle Imaging SpectroRadiometer (MISR). Uncertainty in observational data used in the assimilation is computed by developing different error bands around regional AOD observations, based on their quality assurance flags. The assimilation, evaluated on monthly and daily scales, compares well with Aerosol Robotic Network (AERONET) observations as determined by goodness of fit statistics. Assimilation increased both model predicted atmospheric absorption and clear sky radiative forcing by factors consistent with recent estimates in literature. Thus, the constrained assimilation algorithm helps in systematically reducing uncertainties in aerosol simulations.

  11. Satellite and ground-based remote sensing of aerosols during intense haze event of October 2013 over lahore, Pakistan

    Science.gov (United States)

    Tariq, Salman; Zia, ul-Haq; Ali, Muhammad

    2016-02-01

    Due to increase in population and economic development, the mega-cities are facing increased haze events which are causing important effects on the regional environment and climate. In order to understand these effects, we require an in-depth knowledge of optical and physical properties of aerosols in intense haze conditions. In this paper an effort has been made to analyze the microphysical and optical properties of aerosols during intense haze event over mega-city of Lahore by using remote sensing data obtained from satellites (Terra/Aqua Moderate-resolution Imaging Spectroradiometer (MODIS) and Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observation (CALIPSO)) and ground based instrument (AErosol RObotic NETwork (AERONET)) during 6-14 October 2013. The instantaneous highest value of Aerosol Optical Depth (AOD) is observed to be 3.70 on 9 October 2013 followed by 3.12 on 8 October 2013. The primary cause of such high values is large scale crop residue burning and urban-industrial emissions in the study region. AERONET observations show daily mean AOD of 2.36 which is eight times higher than the observed values on normal day. The observed fine mode volume concentration is more than 1.5 times greater than the coarse mode volume concentration on the high aerosol burden day. We also find high values (~0.95) of Single Scattering Albedo (SSA) on 9 October 2013. Scatter-plot between AOD (500 nm) and Angstrom exponent (440-870 nm) reveals that biomass burning/urban-industrial aerosols are the dominant aerosol type on the heavy aerosol loading day over Lahore. MODIS fire activity image suggests that the areas in the southeast of Lahore across the border with India are dominated by biomass burning activities. A Hybrid Single-Particle Lagrangian Integrated Trajectory (HYSPLIT) model backward trajectory showed that the winds at 1000 m above the ground are responsible for transport from southeast region of biomass burning to Lahore. CALIPSO derived sub-types of

  12. Lidar Observations of Aerosol Disturbances of the Stratosphere over Tomsk (56.5∘N; 85.0∘E in Volcanic Activity Period 2006–2011

    Directory of Open Access Journals (Sweden)

    Oleg E. Bazhenov

    2012-01-01

    Full Text Available The lidar measurements (Tomsk: 56.5∘N; 85.0∘E of the optical characteristics of the stratospheric aerosol layer (SAL in the volcanic activity period 2006–2011 are summarized and analyzed. The background SAL state with minimum aerosol content, observed since 1997 under the conditions of long-term volcanically quiet period, was interrupted in October 2006 by series of explosive eruptions of volcanoes of Pacific Ring of Fire: Rabaul (October 2006, New Guinea; Okmok and Kasatochi (July-August 2008, Aleutian Islands; Redoubt (March-April 2009, Alaska; Sarychev Peak (June 2009, Kuril Islands; Grimsvötn (May 2011, Iceland. A short-term and minor disturbance of the lower stratosphere was also observed in April 2010 after eruption of the Icelandic volcano Eyjafjallajokull. The developed regional empirical model of the vertical distribution of background SAL optical characteristics was used to identify the periods of elevated stratospheric aerosol content after each of the volcanic eruptions. Trends of variations in the total ozone content are also considered.

  13. Aerosol and cloud microphysics covariability in the northeast Pacific boundary layer estimated with ship-based and satellite remote sensing observations: NE Pacific Aerosol-Cloud Interactions

    Energy Technology Data Exchange (ETDEWEB)

    Painemal, David [Science Systems and Applications, Inc., Hampton Virginia USA; NASA Langley Research Center, Hampton Virginia USA; Chiu, J. -Y. Christine [Department of Meteorology, University of Reading, Reading UK; Minnis, Patrick [NASA Langley Research Center, Hampton Virginia USA; Yost, Christopher [Science Systems and Applications, Inc., Hampton Virginia USA; Zhou, Xiaoli [Department of Atmospheric and Oceanic Sciences, McGill University, Montreal Quebec Canada; Cadeddu, Maria [Environmental Science Division, Argonne National Laboratory, Lemont Illinois USA; Eloranta, Edwin [Space Science and Engineering Center, University of Wisconsin-Madison, Madison Wisconsin USA; Lewis, Ernie R. [Brookhaven National Laboratory, Upton New York USA; Ferrare, Richard [NASA Langley Research Center, Hampton Virginia USA; Kollias, Pavlos [School of Marine and Atmospheric Sciences, Stony Brook University, Stony Brook New York USA

    2017-02-27

    Ship measurements collected over the northeast Pacific along transects between the port of Los Angeles (33.7°N, 118.2°W) and Honolulu (21.3°N, 157.8°W) during May to August 2013 were utilized to investigate the covariability between marine low cloud microphysical and aerosol properties. Ship-based retrievals of cloud optical depth (τ) from a Sun photometer and liquid water path (LWP) from a microwave radiometer were combined to derive cloud droplet number concentration Nd and compute a cloud-aerosol interaction (ACI) metric defined as ACICCN = ∂ ln(Nd)/∂ ln(CCN), with CCN denoting the cloud condensation nuclei concentration measured at 0.4% (CCN0.4) and 0.3% (CCN0.3) supersaturation. Analysis of CCN0.4, accumulation mode aerosol concentration (Na), and extinction coefficient (σext) indicates that Na and σext can be used as CCN0.4 proxies for estimating ACI. ACICCN derived from 10 min averaged Nd and CCN0.4 and CCN0.3, and CCN0.4 regressions using Na and σext, produce high ACICCN: near 1.0, that is, a fractional change in aerosols is associated with an equivalent fractional change in Nd. ACICCN computed in deep boundary layers was small (ACICCN = 0.60), indicating that surface aerosol measurements inadequately represent the aerosol variability below clouds. Satellite cloud retrievals from MODerate-resolution Imaging Spectroradiometer and GOES-15 data were compared against ship-based retrievals and further analyzed to compute a satellite-based ACICCN. Satellite data correlated well with their ship-based counterparts with linear correlation coefficients equal to or greater than 0.78. Combined satellite Nd and ship-based CCN0.4 and Na yielded a maximum ACICCN = 0.88–0.92, a value slightly less than the ship-based ACICCN, but still consistent with aircraft-based studies in the eastern Pacific.

  14. Estimation of stratospheric NO2 from nadir-viewing satellites: The MPI-C TROPOMI verification algorithm

    Science.gov (United States)

    Beirle, Steffen; Wagner, Thomas

    2015-04-01

    The retrieval of tropospheric column densities of NO2 requires the subtraction of the stratospheric fraction from the total columns derived by DOAS. Here we present a modified reference sector method, which estimates the stratosphere over "clean" regions, as well as over clouded scenarios in which the tropospheric column is shielded. The selection of "clean" pixels is realized gradually by assingning weighting factors to the individual ground pixels, instead of applying binary flags. Global stratospheric fields are then compiled by "weighted convolution". In a second iteration, unphysical negative tropospheric residues are suppressed by adjusting the weights respectively. This algorithm is foreseen as "verification algorithm" for the upcoming TROPOMI on S5p. We show the resulting stratospheric estimates and tropospheric residues for a test data set based on OMI observations. The dependencies on the a-priori settings (definition of weighting factors and convolution kernels) are discussed, and the results are compared to other products, in particular to DOMINO v.2 (based on assimilation, similar to the TROPOMI prototype algorithm) and the NASA standard product (based on a similar reference-region-type approach).

  15. The Dedicated Aerosol Retrieval Experiment (DARE): scientific requirements for a dedicated satellite instrument to measure atmospheric aerosols

    NARCIS (Netherlands)

    Decae, R.; Courrèges-Lacoste, G.B.; Leeuw, G. de

    2004-01-01

    DARE (Dedicated Aerosol Retrieval Experiment) is a study to design an instrument for accurate remote sensing of aerosol properties from space. DARE combines useful properties of several existing instruments like TOMS, GOME, ATSR and POLDER. It has a large wavelength range, 330 to 1000 nm, to discrim

  16. Characterization of the 3D distribution of ozone and coarse aerosols in the Troposphere using IASI thermal infrared satellite observations

    Science.gov (United States)

    Cuesta, J.; Eremenko, M.; Dufour, G.; Hoepfner, M.; Orphal, J.

    2012-04-01

    Both tropospheric ozone and aerosols significantly affect air quality in megacities during pollution events. Moreover, living conditions may be seriously aggravated when such agglomerations are affected by wildfires (e.g. Russian fires over Moscow in 2010), which produce smoke and pollutant precursors, or even during dense desert dust outbreaks (e.g. recurrently over Beijing or Cairo). Moreover, since aerosols diffuse and absorb solar radiation, they have a direct impact on the photochemical production of tropospheric ozone. These interactions during extreme events of high aerosol loads are nowadays poorly known, even though they may significantly affect the tropospheric photochemical equilibrium. In order to address these issues, we have developed a new retrieval technique to jointly characterize the 3D distribution of both tropospheric ozone and coarse aerosols, using spaceborne observations of the infrared spectrometer IASI onboard MetOp-A satellite. Our methodology is based on the inversion of Earth radiance spectra in the atmospheric window from 8 to 12 μm measured by IASI and a «Tikhonov-Philipps»-type regularisation with constraints varying in altitude (as in [Eremenko et al., 2008, GRL; Dufour et al., 2010 ACP]) to simultaneously retrieve ozone profiles, aerosol optical depths at 10 μm and aerosol layer effective heights. Such joint retrieval prevents biases in the ozone profile retrieval during high aerosol load conditions. Aerosol retrievals using thermal infrared radiances mainly account for desert dust and the coarse fraction of biomass burning aerosols. We use radiances from 15 micro-windows within the 8-12 μm atmospheric window, which were carefully chosen (following [Worden et al., 2006 JGR]) for extracting the maximum information on aerosols and ozone and minimizing contamination by other species. We use the radiative transfer code KOPRA, including line-by-line calculations of gas absorption and single scattering for aerosols [Hoepfner et al

  17. Global Estimates of Average Ground-Level Fine Particulate Matter Concentrations from Satellite-Based Aerosol Optical Depth

    Science.gov (United States)

    Van Donkelaar, A.; Martin, R. V.; Brauer, M.; Kahn, R.; Levy, R.; Verduzco, C.; Villeneuve, P.

    2010-01-01

    Exposure to airborne particles can cause acute or chronic respiratory disease and can exacerbate heart disease, some cancers, and other conditions in susceptible populations. Ground stations that monitor fine particulate matter in the air (smaller than 2.5 microns, called PM2.5) are positioned primarily to observe severe pollution events in areas of high population density; coverage is very limited, even in developed countries, and is not well designed to capture long-term, lower-level exposure that is increasingly linked to chronic health effects. In many parts of the developing world, air quality observation is absent entirely. Instruments aboard NASA Earth Observing System satellites, such as the MODerate resolution Imaging Spectroradiometer (MODIS) and the Multi-angle Imaging SpectroRadiometer (MISR), monitor aerosols from space, providing once daily and about once-weekly coverage, respectively. However, these data are only rarely used for health applications, in part because the can retrieve the amount of aerosols only summed over the entire atmospheric column, rather than focusing just on the near-surface component, in the airspace humans actually breathe. In addition, air quality monitoring often includes detailed analysis of particle chemical composition, impossible from space. In this paper, near-surface aerosol concentrations are derived globally from the total-column aerosol amounts retrieved by MODIS and MISR. Here a computer aerosol simulation is used to determine how much of the satellite-retrieved total column aerosol amount is near the surface. The five-year average (2001-2006) global near-surface aerosol concentration shows that World Health Organization Air Quality standards are exceeded over parts of central and eastern Asia for nearly half the year.

  18. Particulate sulfur in the upper troposphere and lowermost stratosphere - sources and climate forcing

    Science.gov (United States)

    Martinsson, Bengt G.; Friberg, Johan; Sandvik, Oscar S.; Hermann, Markus; van Velthoven, Peter F. J.; Zahn, Andreas

    2017-09-01

    This study is based on fine-mode aerosol samples collected in the upper troposphere (UT) and the lowermost stratosphere (LMS) of the Northern Hemisphere extratropics during monthly intercontinental flights at 8.8-12 km altitude of the IAGOS-CARIBIC platform in the time period 1999-2014. The samples were analyzed for a large number of chemical elements using the accelerator-based methods PIXE (particle-induced X-ray emission) and PESA (particle elastic scattering analysis). Here the particulate sulfur concentrations, obtained by PIXE analysis, are investigated. In addition, the satellite-borne lidar aboard CALIPSO is used to study the stratospheric aerosol load. A steep gradient in particulate sulfur concentration extends several kilometers into the LMS, as a result of increasing dilution towards the tropopause of stratospheric, particulate sulfur-rich air. The stratospheric air is diluted with tropospheric air, forming the extratropical transition layer (ExTL). Observed concentrations are related to the distance to the dynamical tropopause. A linear regression methodology handled seasonal variation and impact from volcanism. This was used to convert each data point into stand-alone estimates of a concentration profile and column concentration of particulate sulfur in a 3 km altitude band above the tropopause. We find distinct responses to volcanic eruptions, and that this layer in the LMS has a significant contribution to the stratospheric aerosol optical depth and thus to its radiative forcing. Further, the origin of UT particulate sulfur shows strong seasonal variation. We find that tropospheric sources dominate during the fall as a result of downward transport of the Asian tropopause aerosol layer (ATAL) formed in the Asian monsoon, whereas transport down from the Junge layer is the main source of UT particulate sulfur in the first half of the year. In this latter part of the year, the stratosphere is the clearly dominating source of particulate sulfur in the UT

  19. Aerosol-Cloud Interactions Over the North Pacific Ocean: an Integrated Assessment Using Aircraft, Satellites and a Global Model

    Science.gov (United States)

    Wilcox, E. M.; Mauger, G.; Lariviere, O.; Roberts, G.; Ramanathan, V.; Ming, Y.

    2004-12-01

    Interactions between aerosols and the cloud systems of the North Pacific Ocean were observed by aircraft during the Cloud Indirect Forcing Experiment (CIFEX) in April 2004. The CIFEX project seeks to determine the impact of aerosol indirect effects on the radiative forcing of highly reflective North Pacific clouds under the influence of aerosols traveling across the ocean basin from Asia. Toward this end, CIFEX aircraft observations from the Northeast Pacific of aerosol and cloud microphysics are blended with coincident satellite observations of cloud properties from MODIS and cloud radiative forcing from CERES. The satellite observations are then compared with global model simulations of aerosol indirect forcing over the entire North Pacific basin. During April 2004 the U. Wyoming King Air research aircraft sampled aerosol and cloud microphysical parameters including aerosol and cloud particle sizes and concentrations, cloud liquid water amounts, and cloud structure using the Wyoming Cloud Radar. A range of clean and polluted conditions were observed by the aircraft during the period, in addition to two major Asian dust storm events. CN concentrations below stratus clouds varied from 25 to 300 cm-3. A variety of cloud systems were sampled as well, ranging from shallow stratus and stratocumulus clouds to mixed-phase precipitating cumulus. Under pristine conditions, many shallow clouds were observed to be drizzling, suggesting that Northern Pacific Ocean cloud systems may be highly susceptible to the influence of aerosols. Clouds in this region are responsible for a large cooling of the ocean surface. The magnitude of shortwave cloud radiative cooling exceeded -80 W m-2 over much of the North Pacific during the experiment. Stratus cloud drop concentrations varied from 25 to 150 cm-3 and are correlated with the concentration of accumulation mode aerosols below cloud base. Mean cloud albedos vary from 0.3 to 0.5 for these same clouds, and MODIS observations of cloud

  20. Satellite-Observed Urbanization Characters in Shanghai, China: Aerosols, Urban Heat Island Effect, and Land–Atmosphere Interactions

    Directory of Open Access Journals (Sweden)

    Gary Pereira

    2011-01-01

    Full Text Available Urbanization reflects how human-activities affect natural climate system. Accurately assessing the urban system by comparing it with the nearby rural regions helps to identify the impacts of urbanization. This work uses the recent satellite observed aerosol, skin temperature, land cover, albedo, cloud fraction and water vapor measurements to reveal how the city of Shanghai, one of the biggest, dense urban areas in East Asia, affects land surface and atmosphere conditions. In addition, the National Aeronautics and Space Administration (NASA ground observations from AErosol RObotic NETwork (AERONET is also used to reveal diurnal, seasonal, and interannual variations of the heavy aerosol load over Shanghai region. Furthermore, Shanghai reduces surface albedo, total column water vapor, cloud fraction and increases land skin temperature than rural region. These observations prove that Shanghai significantly modifies local and regional land surface physical properties as well as physical processes, which lead to the urban heat island effect (UHI.

  1. Issues in Data Fusion for Satellite Aerosol Measurements for Applications with GIOVANNI System at NASA GES DISC

    Science.gov (United States)

    Gopalan, Arun; Zubko, Viktor; Leptoukh, Gregory G.

    2008-01-01

    We look at issues, barriers and approaches for Data Fusion of satellite aerosol data as available from the GES DISC GIOVANNI Web Service. Daily Global Maps of AOT from a single satellite sensor alone contain gaps that arise due to various sources (sun glint regions, clouds, orbital swath gaps at low latitudes, bright underlying surfaces etc.). The goal is to develop a fast, accurate and efficient method to improve the spatial coverage of the Daily AOT data to facilitate comparisons with Global Models. Data Fusion may be supplemented by Optimal Interpolation (OI) as needed.

  2. Use of satellite-based aerosol optical depth and spatial clustering to predict ambient PM2.5 concentrations

    OpenAIRE

    2012-01-01

    Satellite-based PM2.5 monitoring has the potential to complement ground PM2.5 monitoring networks, especially for regions with sparsely distributed monitors. Satellite remote sensing provides data on aerosol optical depth (AOD), which reflects particle abundance in the atmospheric column. Thus AOD has been used in statistical models to predict ground-level PM2.5 concentrations. However, previous studies have shown that AOD may not be a strong predictor of PM2.5 ground levels. Another shortcom...

  3. Polarization studies of the Earth stratospheric layer by means of picosatellite

    Science.gov (United States)

    Zbrutskyi, O. V.; Saryboha, H. V.; Nevodovskyi, P. V.; Vidmachenko, A. P.; Ivakhiv, O. V.

    2016-10-01

    Changes of aerosol optical thickness in the upper layers of Earth's atmosphere is one of the reasons that lead to climate change on Earth. Stratospheric ozone layer completely absorbs solar radiation. So polarimetric measurements of aerosol in the ultraviolet (UV) part of the spectrum to effectively carry out research into the causes of these changes. This problem can be solved by means of remote sensing of the ozone layer from the board of space satellite with the use of ultraviolet polarimeter. On the development of such devices actively working researchers of different countries.

  4. Mixing between a stratospheric intrusion and a biomass burning plume

    Directory of Open Access Journals (Sweden)

    J. Brioude

    2007-08-01

    Full Text Available Ozone, carbon monoxide, aerosol extinction coefficient, acetonitrile, nitric acid and relative humidity measured from the NOAA P3 aircraft during the TexAQS/GoMACCS 2006 experiment, indicate mixing between a biomass burning plume and a stratospheric intrusion in the free troposphere above eastern Texas. Lagrangian-based transport analysis and satellite imagery are used to investigate the transport mechanisms that bring together the tropopause fold and the biomass burning plume originating in southern California, which may affect the chemical budget of tropospheric trace gases.

  5. Mixing between a stratospheric intrusion and a biomass burning plume

    Directory of Open Access Journals (Sweden)

    J. Brioude

    2007-06-01

    Full Text Available Ozone, carbon monoxide, aerosol extinction coefficient, acetonitrile, nitric acid and relative humidity measured from the NOAA P3 aircraft during the TexAQS/GoMACCS 2006 experiment, indicate mixing between a biomass burning plume and a stratospheric intrusion in the free troposphere above eastern Texas. Lagrangian-based transport analysis and satellite imagery are used to investigate the transport mechanisms that bring together the tropopause fold and the biomass burning plume originating in southern California, which may affect the chemical budget of tropospheric trace gases.

  6. Statistically optimized inversion algorithm for enhanced retrieval of aerosol properties from spectral multi-angle polarimetric satellite observations

    Science.gov (United States)

    Dubovik, O.; Herman, M.; Holdak, A.; Lapyonok, T.; Tanré, D.; Deuzé, J. L.; Ducos, F.; Sinyuk, A.; Lopatin, A.

    2011-05-01

    The proposed development is an attempt to enhance aerosol retrieval by emphasizing statistical optimization in inversion of advanced satellite observations. This optimization concept improves retrieval accuracy relying on the knowledge of measurement error distribution. Efficient application of such optimization requires pronounced data redundancy (excess of the measurements number over number of unknowns) that is not common in satellite observations. The POLDER imager on board the PARASOL micro-satellite registers spectral polarimetric characteristics of the reflected atmospheric radiation at up to 16 viewing directions over each observed pixel. The completeness of such observations is notably higher than for most currently operating passive satellite aerosol sensors. This provides an opportunity for profound utilization of statistical optimization principles in satellite data inversion. The proposed retrieval scheme is designed as statistically optimized multi-variable fitting of all available angular observations obtained by the POLDER sensor in the window spectral channels where absorption by gas is minimal. The total number of such observations by PARASOL always exceeds a hundred over each pixel and the statistical optimization concept promises to be efficient even if the algorithm retrieves several tens of aerosol parameters. Based on this idea, the proposed algorithm uses a large number of unknowns and is aimed at retrieval of extended set of parameters affecting measured radiation. The algorithm is designed to retrieve complete aerosol properties globally. Over land, the algorithm retrieves the parameters of underlying surface simultaneously with aerosol. In all situations, the approach is anticipated to achieve a robust retrieval of complete aerosol properties including information about aerosol particle sizes, shape, absorption and composition (refractive index). In order to achieve reliable retrieval from PARASOL observations even over very reflective

  7. Statistically optimized inversion algorithm for enhanced retrieval of aerosol properties from spectral multi-angle polarimetric satellite observations

    Directory of Open Access Journals (Sweden)

    O. Dubovik

    2011-05-01

    Full Text Available The proposed development is an attempt to enhance aerosol retrieval by emphasizing statistical optimization in inversion of advanced satellite observations. This optimization concept improves retrieval accuracy relying on the knowledge of measurement error distribution. Efficient application of such optimization requires pronounced data redundancy (excess of the measurements number over number of unknowns that is not common in satellite observations. The POLDER imager on board the PARASOL micro-satellite registers spectral polarimetric characteristics of the reflected atmospheric radiation at up to 16 viewing directions over each observed pixel. The completeness of such observations is notably higher than for most currently operating passive satellite aerosol sensors. This provides an opportunity for profound utilization of statistical optimization principles in satellite data inversion. The proposed retrieval scheme is designed as statistically optimized multi-variable fitting of all available angular observations obtained by the POLDER sensor in the window spectral channels where absorption by gas is minimal. The total number of such observations by PARASOL always exceeds a hundred over each pixel and the statistical optimization concept promises to be efficient even if the algorithm retrieves several tens of aerosol parameters. Based on this idea, the proposed algorithm uses a large number of unknowns and is aimed at retrieval of extended set of parameters affecting measured radiation.

    The algorithm is designed to retrieve complete aerosol properties globally. Over land, the algorithm retrieves the parameters of underlying surface simultaneously with aerosol. In all situations, the approach is anticipated to achieve a robust retrieval of complete aerosol properties including information about aerosol particle sizes, shape, absorption and composition (refractive index. In order to achieve reliable retrieval from PARASOL observations

  8. Statistically optimized inversion algorithm for enhanced retrieval of aerosol properties from spectral multi-angle polarimetric satellite observations

    Directory of Open Access Journals (Sweden)

    O. Dubovik

    2010-11-01

    Full Text Available The proposed development is an attempt to enhance aerosol retrieval by emphasizing statistical optimization in inversion of advanced satellite observations. This optimization concept improves retrieval accuracy relying on the knowledge of measurement error distribution. Efficient application of such optimization requires pronounced data redundancy (excess of the measurements number over number of unknowns that is not common in satellite observations. The POLDER imager on board of the PARASOL micro-satellite registers spectral polarimetric characteristics of the reflected atmospheric radiation at up to 16 viewing directions over each observed pixel. The completeness of such observations is notably higher than for most currently operating passive satellite aerosol sensors. This provides an opportunity for profound utilization of statistical optimization principles in satellite data inversion. The proposed retrieval scheme is designed as statistically optimized multi-variable fitting of the all available angular observations of total and polarized radiances obtained by POLDER sensor in the window spectral channels where absorption by gaseous is minimal. The total number of such observations by PARASOL always exceeds a hundred over each pixel and the statistical optimization concept promises to be efficient even if the algorithm retrieves several tens of aerosol parameters. Based on this idea, the proposed algorithm uses a large number of unknowns and is aimed on retrieval of extended set of parameters affecting measured radiation.

    The algorithm is designed to retrieve complete aerosol properties globally. Over land, the algorithm retrieves the parameters of underlying surface simultaneously with aerosol. In all situations, the approach is anticipated to achieve a robust retrieval of complete aerosol properties including information about aerosol particle sizes, shape, absorption and composition (refractive index. In order to achieve

  9. Multi-Grid-Cell Validation of Satellite Aerosol Property Retrievals in INTEX/ITCT/ICARTT 2004

    Science.gov (United States)

    Russell, P. B.; Livingston, J. M.; Redemann, J.; Schmid, B.; Ramirez, S. A.; Eilers, J.; Kahn, R.; Chu, D. A.; Remer, L.; Quinn, P. K.; Rood, M. J.; Wang, W.

    2007-01-01

    Aerosol transport off the US Northeast coast during the Summer 2004 International Consortium for Atmospheric Research on Transport and Transformation (ICARTT) Intercontinental Chemical Transport Experiment (INTEX) and Intercontinental Transport and Chemical Transformation (ITCT) experiments produced a wide range of aerosol types and aerosol optical depth (AOD) values, often with strong horizontal AOD gradients. In these conditions we flew the 14-channel NASA Ames Airborne Tracking Sun photometer (AATS) on a Jetstream 31 (J31) aircraft. Legs flown at low altitude (usually less than 100 m ASL) provided comparisons of AATS AOD spectra to retrievals for 90 grid cells of the satellite radiometers MODIS-Terra, MODIS-Aqua, and MISR, all over the ocean. Characterization of the retrieval environment was aided by using vertical profiles by the J31 (showing aerosol vertical structure) and, on occasion, shipboard measurements of light scattering and absorption. AATS provides AOD at 13 wavelengths lambda from 354 to 2138 nm, spanning the range of aerosol retrieval wavelengths for MODIS over ocean (466-2119 nm) and MISR (446-866 nm). Midvisible AOD on low-altitude J31 legs in satellite grid cells ranged from 0.05 to 0.9, with horizontal gradients often in the range 0.05 to 0.13 per 10 km. When possible, we used ship measurements of humidified aerosol scattering and absorption to estimate AOD below the J31. In these cases, which had J31 altitudes 60-110 m ASL (typical of J31 low-altitude transects), estimated midvisible AOD below the J31 ranged from 0.003 to 0.013, with mean 0.009 and standard deviation 0.003. These values averaged 6 percent of AOD above the 53 1. MISR-AATS comparisons on 29 July 2004 in 8 grid cells (each -17.6 km x 17.6 km) show that MISR versions 15 and 16 captured the AATS-measured AOD gradient (correlation coefficient R2 = 0.87 to 0.92), but the MISR gradient was somewhat weaker than the AATS gradient. The large AOD (midvisible values up to -0.9) and

  10. Dust aerosol impact on the retrieval of cloud top height from satellite observations of CALIPSO, CloudSat and MODIS

    Science.gov (United States)

    Wang, Wencai; Sheng, Lifang; Dong, Xu; Qu, Wenjun; Sun, Jilin; Jin, Hongchun; Logan, Timothy

    2017-02-01

    Dust aerosol effect on the retrievals of dusty cloud top height (DCTH) are analyzed over Northwest China using cloud products from MODerate Resolution Imaging Spectroradiometer (MODIS) on Aqua, Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observations (CALIPSO), and CloudSat for the Spring season of March-May over the years 2007-2011. An excellent agreement is found between CloudSat and CALIPSO derived DCTHs for all cloud types, suggesting that the effect of dust aerosols plays a small role in DCTHs determination for lidar and radar measurements. However, the presence of dust aerosols greatly affects the retrievals of DCTHs for MODIS compared with pure clouds and the active sensors derived results. The differences of DCTHs retrieving from CloudSat and MODIS range from -2.30 to 6.8 km. Likewise, the differences of DCTHs retrieving from CALIPSO and MODIS range from -2.66 to 6.78 km. In addition, the results show that the differences in DCTHs for active and passive sensors are dependent on cloud type. On the whole, dust aerosols have the largest effect on cloud top heights (CTH) retrieved of nimbostratus (Ns), followed by altocumulus (Ac) and altostratus (As), the last is cirrus (Ci) over Northwest China. Our results also indicate that the accuracy of MODIS-derived retrievals reduces accompanied with a decrease of height.

  11. Technical Note: A novel rocket-based in situ collection technique for mesospheric and stratospheric aerosol particles

    Directory of Open Access Journals (Sweden)

    W. Reid

    2013-03-01

    Full Text Available A technique for collecting aerosol particles between altitudes of 17 and 85 km is described. Spin-stabilized collection probes are ejected from a sounding rocket allowing for multi-point measurements. Each probe is equipped with 110 collection samples that are 3 mm in diameter. The collection samples are one of three types: standard transmission electron microscopy carbon grids, glass fibre filter paper or silicone gel. Collection samples are exposed over a 50 m to 5 km height range with a total of 45 separate ranges. Post-flight electron microscopy will give size-resolved information on particle number, shape and elemental composition. Each collection probe is equipped with a suite of sensors to capture the probe's status during the fall. Parachute recovery systems along with GPS-based localization will ensure that each probe can be located and recovered for post-flight analysis.

  12. Spatio-temporal characteristics of aerosol distribution over Tibetan Plateau and numerical simulation of radiative forcing and climate response

    Institute of Scientific and Technical Information of China (English)

    李维亮; 于胜民

    2001-01-01

    In this paper we have analyzed aerosol distribution over the Tibetan Plateau by using the global monthly mean satellite data of Stratospheric Aerosol and Gas Experiment Ⅱ (SAGE Ⅱ).The results are as follows: (1) Stratospheric aerosol optical depth can oscillate in the four seasons. It means that the aerosol optical depth is the thickest in winter and a little thinner in spring and the thinnest in summer and then a little thicker in autumn. We have found that the oscillation is caused by the oscillation of tropopause in different seasons. (2) Stratospheric aerosol comes mainly from sprays of volcano. After eruption of Mount Pinatubo aerosol optical depth in stratosphere over the Tibetan Plateau increases 10 times compared with before. (3) The characteristic of aerosol vertical distribution over the Tibetan Plateau is that there is an extremely high value at the altitude of 70 hPa. The most interesting thing is that the extremely high value can oscillate between 50 hPa and 100 hPa. We have verified that

  13. Regional and monthly and clear-sky aerosol direct radiative effect (and forcing derived from the GlobAEROSOL-AATSR satellite aerosol product

    Directory of Open Access Journals (Sweden)

    G. E. Thomas

    2013-01-01

    Full Text Available Using the GlobAEROSOL-AATSR dataset, estimates of the instantaneous, clear-sky, direct aerosol radiative effect and radiative forcing have been produced for the year 2006. Aerosol Robotic Network sun-photometer measurements have been used to characterise the random and systematic error in the GlobAEROSOL product for 22 regions covering the globe. Representative aerosol properties for each region were derived from the results of a wide range of literature sources and, along with the de-biased GlobAEROSOL AODs, were used to drive an offline version of the Met Office unified model radiation scheme. In addition to the mean AOD, best-estimate run of the radiation scheme, a range of additional calculations were done to propagate uncertainty estimates in the AOD, optical properties, surface albedo and errors due to the temporal and spatial averaging of the AOD fields. This analysis produced monthly, regional estimates of the clear-sky aerosol radiative effect and its uncertainty, which were combined to produce annual, global mean values of (−6.7 ± 3.9 W m−2 at the top of atmosphere (TOA and (−12 ± 6 W m−2 at the surface. These results were then used to give estimates of regional, clear-sky aerosol direct radiative forcing, using modelled pre-industrial AOD fields for the year 1750 calculated for the AEROCOM PRE experiment. However, as it was not possible to quantify the uncertainty in the pre-industrial aerosol loading, these figures can only be taken as indicative and their uncertainties as lower bounds on the likely errors. Although the uncertainty on aerosol radiative effect presented here is considerably larger than most previous estimates, the explicit inclusion of the major sources of error in the calculations suggest that they are closer to the true constraint on this figure from similar methodologies, and point to the need for more, improved estimates of both global aerosol loading and aerosol optical properties.

  14. Regional and monthly and clear-sky aerosol direct radiative effect (and forcing derived from the GlobAEROSOL-AATSR satellite aerosol product

    Directory of Open Access Journals (Sweden)

    G. E. Thomas

    2012-07-01

    Full Text Available Using the GlobAEROSOL-AATSR dataset, estimates of the instantaneous, clear-sky, direct aerosol radiative effect and radiative forcing have been produced for the year 2006. Aerosol Robotic Network sun-photometer measurements have been used to characterise the random and systematic error in the GlobAEROSOL product for 22 regions covering the globe. Representative aerosol properties for each region have been derived from the results of a wide range of literature sources and, along with the de-biased GlobAEROSOL AODs, were used to drive an offline version of the Met Office unified model radiation scheme. In addition to the mean AOD, best-estimate run of the radiation scheme, a range of additional calculations were done to propagate uncertainty estimates in the AOD, optical properties, surface albedo and errors due to the temporal and spatial averaging of the AOD fields. This analysis produced monthly, regional estimates of the clear-sky aerosol radiative effect and its uncertainty, which produce annual, global mean values of (−6.7 ± 3.9 W m−2 at the top of atmosphere (TOA and (−12 ± 6 W m−2 at the surface. These results were then used to produce estimates of regional, clear-sky aerosol direct radiative forcing, using modelled pre-industrial AOD fields for 1750 calculated for the AEROCOM PRE experiment. However, as it was not possible to quantify the uncertainty in the pre-industrial aerosol loading, these figures can only be taken as indicative and their uncertainties as lower bounds on the likely errors. Although the uncertainty on aerosol radiative effect presented here is considerably larger than most previous estimates, the explicit inclusion of the major sources of error in the calculations suggest that they are closer to the true constraint on this figure from similar methodologies, and point to the need for more, improved estimates of both global aerosol loading and aerosol optical properties.

  15. Assessment of the aerosol optical depths measured by satellite-based passive remote sensors in the Alberta oil sands region

    Science.gov (United States)

    Sioris, Christopher E.; McLinden, Chris A.; Shephard, Mark W.; Fioletov, Vitali E.; Abboud, Ihab

    2017-02-01

    Several satellite aerosol optical depth (AOD) products are assessed in terms of their data quality in the Alberta oil sands region. The instruments consist of MODIS (Moderate Resolution Imaging Spectroradiometer), POLDER (Polarization and Directionality of Earth Reflectances), MISR (Multi-angle Imaging SpectroRadiometer), and AATSR (Advanced Along-Track Scanning Radiometer). The AOD data products are examined in terms of multiplicative and additive biases determined using local Aerosol Robotic Network (AERONET) (AEROCAN) stations. Correlation with ground-based data is used to assess whether the satellite-based AODs capture day-to-day, month-to-month, and spatial variability. The ability of the satellite AOD products to capture interannual variability is assessed at Albian mine and Shell Muskeg River, two neighbouring sites in the northern mining region where a statistically significant positive trend (2002-2015) in PM2.5 mass density exists. An increasing trend of similar amplitude (˜ 5 % year-1) is observed in this northern mining region using some of the satellite AOD products.

  16. The Relation of Stratospheric Aerosols with Trace Gases and Temperature%平流层气溶胶与多种微量气体以及温度的关系

    Institute of Scientific and Technical Information of China (English)

    蔡宏珂; 郭静超; 周任君; 刘鹏兵; 傅云飞

    2011-01-01

    The HALOE (Halogen Occultation Experiment) dataset is used to study the relation of stratospheric aerosols with trace gases (O3, H2O, HC1, NOX, CH4, and HF) and temperature in a period of relative volcanic quiescence. The lag-correlation analysis shows trace gases and temperature are significantly related to aerosol surface area density. Characteristics of the relevance vary with different components. Temperature is negatively correlated with aerosol for 70 - 20 hPa over low-and mid-latitudes. Standardized multiple linear regression demonstrates that greenhouse gases are the primary direct contributor for temperature change, and the direct contribution of aerosols is much less. The impact of aerosols on the stratosphere is simulated with the two-dimensional model SOCRATES (Simulation of Chemistry, Radiation, and Transport of Environmentally important Species). The response of trace gases and temperature coincides with the analysis of the HALOE. The rangeability of temperature is much less than that of aerosols. The result suggests that the stratospheric heterogeneous processes on aerosol surfaces are important for the relation between aerosols and trace gases in the aerosol-enriched layers. The radiation effect of aerosolsis cooling in the period of relative volcanic quiescence, which is different from the warming effect after volcanic eruptions. The phenomenon depends on the aerosol contents. The indirect radiation effect via heterogeneous processes is stronger than the direct effect of aerosols themselves, but the total radiation effect makes little impact on temperature.%本文采用卤素掩星试验(Halogen Occultation Experiment,HALOE)资料探讨了火山活动相对平静期平流层气溶胶与O3、H2O、HC1、NOx、CH4、HF等微量气体以及温度的关系.滞后相关分析显示气溶胶与微量气体和温度有显著关系,不同成分的相关性特征有所差异,中低纬度上空70~20 hPa高度上气溶胶与温度旱负相关.标准化多

  17. Analysis of the Interaction and Transport of Aerosols with Cloud or Fog in East Asia from AERONET and Satellite Remote Sensing: 2012 DRAGON Campaigns and Climatological Data

    Science.gov (United States)

    Eck, T. F.; Holben, B. N.; Reid, J. S.; Lynch, P.; Schafer, J.; Giles, D. M.; Kim, J.; Kim, Y. J.; Sano, I.; Arola, A. T.; Munchak, L. A.; O'Neill, N. T.; Lyapustin, A.; Sayer, A. M.; Hsu, N. Y. C.; Randles, C. A.; da Silva, A. M., Jr.; Govindaraju, R.; Hyer, E. J.; Pickering, K. E.; Crawford, J. H.; Sinyuk, A.; Smirnov, A.

    2015-12-01

    Ground-based remote sensing observations from Aerosol Robotic Network (AERONET) sun-sky radiometers have recently shown several instances where cloud-aerosol interaction had resulted in modification of aerosol properties and/or in difficulty identifying some major pollution transport events due to aerosols being imbedded in cloud systems. Major Distributed Regional Aerosol Gridded Observation Networks (DRAGON) field campaigns involving multiple AERONET sites in Japan and South Korea during Spring of 2012 have yielded observations of aerosol transport associated with clouds and/or aerosol properties modification as a result of fog interaction. Analysis of data from the Korean and Japan DRAGON campaigns shows that major fine-mode aerosol transport events are sometimes associated with extensive cloud cover and that cloud-screening of observations often filter out significant pollution aerosol transport events. The Spectral De-convolution Algorithm (SDA) algorithm was utilized to isolate and analyze the fine-mode aerosol optical depth (AODf) signal from AERONET data for these cases of persistent and extensive cloud cover. Satellite retrievals of AOD from MODIS sensors (from Dark Target, Deep Blue and MAIAC algorithms) were also investigated to assess the issue of detectability of high AOD events associated with high cloud fraction. Underestimation of fine mode AOD by the Navy Aerosol Analysis and Prediction System (NAAPS) and by the NASA Modern-Era Retrospective Analysis For Research And Applications Aerosol Re-analysis (MERRAaero) models at very high AOD at sites in China and Korea was observed, especially for observations that are cloud screened by AERONET (Level 2 data). Additionally, multi-year monitoring at several AERONET sites are examined for climatological statistics of cloud screening of fine mode aerosol events. Aerosol that has been affected by clouds or the near-cloud environment may be more prevalent than AERONET data suggest due to inherent difficulty in

  18. Intercomparison of stratospheric nitrogen dioxide columns retrieved from ground-based DOAS and FTIR and satellite DOAS instruments over the subtropical Izana station

    Science.gov (United States)

    Robles-Gonzalez, Cristina; Navarro-Comas, Mónica; Puentedura, Olga; Schneider, Matthias; Hase, Frank; Garcia, Omaira; Blumenstock, Thomas; Gil-Ojeda, Manuel

    2016-09-01

    A 13-year analysis (2000-2012) of the NO2 vertical column densities derived from ground-based (GB) instruments and satellites has been carried out over the Izaña NDACC (Network for the Detection of the Atmospheric Composition Change) subtropical site. Ground-based DOAS (differential optical absorption spectroscopy) and FTIR (Fourier transform infrared spectroscopy) instruments are intercompared to test mutual consistency and then used for validation of stratospheric NO2 from OMI (Ozone Monitoring Instrument) and SCIAMACHY (SCanning Imaging Absorption spectroMeter for Atmospheric CHartographY). The intercomparison has been carried out taking into account the various differences existing in instruments, namely temporal coincidence, collocation, sensitivity, field of view, etc. The paper highlights the importance of considering an "effective solar zenith angle" instead of the actual one when comparing direct-sun instruments with zenith sky ones for a proper photochemical correction. Results show that NO2 vertical column densities mean relative difference between FTIR and DOAS instruments is 2.8 ± 10.7 % for a.m. data. Both instruments properly reproduce the NO2 seasonal and the interannual variation. Mean relative difference of the stratospheric NO2 derived from OMI and DOAS is -0.2 ± 8.7 % and from OMI and FTIR is -1.6 ± 6.7 %. SCIAMACHY mean relative difference is of 3.7 ± 11.7 and -5.7 ± 11.0 % for DOAS and FTIR, respectively. Note that the days used for the intercomparison are not the same for all the pairs of instruments since it depends on the availability of data. The discrepancies are found to be seasonally dependent with largest differences in winter and excellent agreement in the spring months (AMJ). A preliminary analysis of NO2 trends has been carried out with the available data series. Results show increases in stratospheric NO2 columns in all instruments but larger values in those that are GB than that expected by nitrous oxide oxidation. The

  19. Reevaluation of Mineral aerosol radiative forcings suggests a better agreement with satellite and AERONET data

    Directory of Open Access Journals (Sweden)

    Y. Balkanski

    2007-01-01

    Full Text Available Modelling studies and satellite retrievals do not agree on the amplitude and/or sign of the direct radiative perturbation from dust. Modelling studies have systematically overpredicted mineral dust absorption compared to estimates based upon satellite retrievals. In this paper we first point out the source of this discrepancy, which originates from the shortwave refractive index of dust used in models. The imaginary part of the refractive index retrieved from AERONET over the range 300 to 700 nm is 3 to 6 times smaller than that used previously to model dust. We attempt to constrain these refractive indices using a mineralogical database and varying the abundances of iron oxides (the main absorber in the visible. We first consider the optically active mineral constituents of dust and compute the refractive indices from internal and external mixtures of minerals with relative amounts encountered in parent soils. We then compute the radiative perturbation due to mineral aerosols for internally and externally mixed minerals for 3 different hematite contents, 0.9%, 1.5% and 2.7% by volume. These constant amounts of hematite allow bracketing the influence of dust aerosol when it is respectively an inefficient, standard and a very efficient absorber. These values represent low, central and high content of iron oxides in dust determined from the mineralogical database. Linke et al. (2006 determined independently that iron-oxides represent 1.0 to 2.5% by volume using x-Ray fluorescence on 4 different samples collected over Morocco and Egypt. Based upon values of the refractive index retrieved from AERONET, we show that the best agreement between 440 and 1020 nm occurs for mineral dust internally mixed with 1.5% volume weighted hematite. This representation of mineral dust allows us to compute, using a general circulation model, a new global estimate of mineral dust perturbation between –0.47 and –0.24 Wm−2 at the top of the atmosphere, and between

  20. Comparison of ground based indices (API and AQI) with satellite based aerosol products.

    Science.gov (United States)

    Zheng, Sheng; Cao, Chun-Xiang; Singh, Ramesh P

    2014-08-01

    Air quality in mega cities is one of the major concerns due to serious health issues and its indirect impact to the climate. Among mega cities, Beijing city is considered as one of the densely populated cities with extremely poor air quality. The meteorological parameters (wind, surface temperature, air temperature and relative humidity) control the dynamics and dispersion of air pollution. China National Environmental Monitoring Centre (CNEMC) started air pollution index (API) as of 2000 to evaluate air quality, but over the years, it was felt that the air quality is not well represented by API. Recently, the Ministry of Environmental Protection (MEP) of the People's Republic of China (PRC) started using a new index "air quality index (AQI)" from January 2013. We have compared API and AQI with three different MODIS (MODIS - Moderate Resolution Imaging SpectroRadiometer, onboard the Terra/Aqua satellites) AOD (aerosol optical depth) products for ten months, January-October, 2013. The correlation between AQI and Aqua Deep Blue AOD was found to be reasonably good as compared with API, mainly due to inclusion of PM2.5 in the calculation of AQI. In addition, for every month, the correlation coefficient between AQI and Aqua Deep Blue AOD was found to be relatively higher in the month of February to May. According to the monthly average distribution of precipitation, temperature, and PM10, the air quality in the months of June-September was better as compared to those in the months of February-May. AQI and Aqua Deep Blue AOD show highly polluted days associated with dust event, representing true air quality of Beijing.

  1. Aerosol measurements over South Africa using LIDAR, Satellite and Sun Photometer

    CSIR Research Space (South Africa)

    Sivakumar, V

    2010-05-01

    Full Text Available of South Africa. 1. Introduction Aerosols (solid particles suspended in the air) play an important role in the global climate, the radiative forcing of the climate, and the Earth?s radiative balance. The interaction between atmospheric aerosol... pollution as well as from natural processes, such as wind generated dust and sea spray, volcanic eruptions and smoke from natural forest fires, etc. The knowledge of aerosol characteristics at a local and global scale, their temporal change interrelations...

  2. TOMS Absorbing Aerosol Index

    Data.gov (United States)

    Washington University St Louis — TOMS_AI_G is an aerosol related dataset derived from the Total Ozone Monitoring Satellite (TOMS) Sensor. The TOMS aerosol index arises from absorbing aerosols such...

  3. Deriving the effect of wind speed on clean marine aerosol optical properties using the A-Train satellites

    Directory of Open Access Journals (Sweden)

    V. P. Kiliyanpilakkil

    2011-11-01

    Full Text Available The relationship between "clean marine" aerosol optical properties and ocean surface wind speed is explored using remotely sensed data from the Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP on board the CALIPSO satellite and the Advanced Microwave Scanning Radiometer (AMSR-E on board the AQUA satellite. Detailed data analyses are carried out over 15 regions selected to be representative of different areas of the global ocean for the time period from June 2006 to April 2011. Based on remotely sensed optical properties the CALIPSO algorithm is capable of discriminating "clean marine" aerosols from other types often present over the ocean (such as urban/industrial pollution, desert dust and biomass burning. The global mean optical depth of "clean marine" aerosol at 532 nm (AOD532 is found to be 0.052 ± 0.038 (mean plus or minus standard deviation. The mean layer integrated particulate depolarization ratio of marine aerosols is 0.02 ± 0.016. Integrated attenuated backscatter and color ratio of marine aerosols at 532 nm were found to be 0.003 ± 0.002 sr−1 and 0.530 ± 0.149, respectively. A logistic regression between AOD532 and 10-m surface wind speed (U10 revealed three distinct regimes. For U10 ≤ 4 m s−1 the mean CALIPSO-derived AOD532 is found to be 0.02 ± 0.003 with little dependency on the surface wind speed. For 4 < U10 ≤ 12 m s−1, representing the dominant fraction of all available data, marine aerosol optical depth is linearly correlated with the surface wind speed values, with a slope of 0.006 s m−1. In this intermediate wind speed region, the AOD532 vs. U10 regression slope derived here is comparable to previously reported values. At very high wind speed values (U10 > 18 m s−1, the AOD532-wind speed relationship

  4. Rare Isotope Insights into Supereruptions: Rare Sulfur and Triple Oxygen Isotope Geochemistry of Stratospheric Sulfate Aerosols Absorbed on Volcanic Ash Particles

    Science.gov (United States)

    Bindeman, I. N.; Eiler, J.; Wing, B.; Farquhar, J.

    2006-12-01

    We present analyses of stable isotopic ratios of 17O/16O, 18O/16O, 34S/32S, and 33S/32S, 36S/32S of sulfate leached from volcanic ash of a series of well-known volcanic eruptions. This list covers much of the diversity of sizes and the character of volcanic eruptions. Particular emphasis is paid to the Lava Creek Tuff of Yellowstone and we present wide geographic sample coverage for this unit. This global dataset spans a significant range in δ34S, δ18O, and Δ17O of sulfate (29, 30 and 3.3 permil respectively) with oxygen isotopes recording mass-independent fractionation and sulfur isotopes exhibiting mass-dependent behavior. These ranges are defined by the isotopic compositions of products of large caldera forming eruptions. Proximal ignimbrites and coarse ash typically do not contain sulfate. The presence of sulfate with Δ17O > 0.2 permil is characteristic of small distal ash particles, suggesting that sulfate aerosols were scavenged after they underwent atmospheric photochemical reactions. Additionally, sediments that embed ash layers either do not contain sulfate or contain minor sulfate with Δ17O near 0 permil, suggesting that the observed sulfate in ash is of volcanic origin. Mass-dependent sulfur isotopic compositions suggest that sulfate-forming reactions did not involve photolysis of SO2, unlike the situation inferred for some pre-2.3 Ga sulfates or hypothesized to occur during the formation of sulfate associated with plinian eruptions that pierce the ozone layer. However, sulfate in the products of caldera-forming eruptions display a large δ34S range and fractionation relationships that do not follow equilibrium slopes of 0.515 and 1.90 for 33S/32S vs. 34S/32S and 36S/32S vs. 34S/32S, respectively. This implies that the sulfur isotopic characteristics of these sulfates were not set by a single stage, high-temperature equilibrium process in the volcanic plum. The data presented here are consistent with a single stage kinetic fractionation of sulfur

  5. Sensitivity of polar stratospheric cloud formation to changes in water vapour and temperature

    Directory of Open Access Journals (Sweden)

    F. Khosrawi

    2015-07-01

    Full Text Available More than a decade ago it was suggested that a cooling of stratospheric temperatures by 1 K or an increase of 1 ppmv of stratospheric water vapour could promote denitrification, the permanent removal of nitrogen species from the stratosphere by solid polar stratospheric cloud (PSC particles. In fact, during the two Arctic winters 2009/10 and 2010/11 the strongest denitrification in the recent decade was observed. Sensitivity studies along air parcel trajectories are performed to test how a future stratospheric water vapour (H2O increase of 1 ppmv or a temperature decrease of 1 K would affect PSC formation. We perform our study based on measurements made during the Arctic winter 2010/11. Air parcel trajectories were calculated 6 days backward in time based on PSCs detected by CALIPSO (Cloud Aerosol Lidar and Infrared Pathfinder satellite observations. The sensitivity study was performed on single trajectories as well as on a trajectory ensemble. The sensitivity study shows a clear prolongation of the potential for PSC formation and PSC existence when the temperature in the stratosphere is decreased by 1 K and water vapour is increased by 1 ppmv. Based on 15 years of satellite measurements (2000–2014 from UARS/HALOE, Envisat/MIPAS, Odin/SMR, Aura/MLS, Envisat/SCIAMACHY and SCISAT/ACE-FTS it is further investigated if there is a decrease in temperature and/or increase of water vapour (H2O observed in the polar regions similar to that observed at midlatitudes and in the tropics. Although in the polar regions no significant trend is found in the lower stratosphere, we found from the observations a correlation between cold winters and enhanced water vapour mixing ratios.

  6. Solar response in tropical stratospheric ozone: a 3-D chemical transport model study using ERA reanalyses

    Directory of Open Access Journals (Sweden)

    S. Dhomse

    2011-12-01

    Full Text Available We have used an off-line 3-D chemical transport model (CTM to investigate the 11-yr solar cycle response in tropical stratospheric ozone. The model is forced with European Centre for Medium-Range Weather Forecasts (ECMWF (reanalysis (ERA-40/operational and ERA-Interim data for the 1979–2005 time period. We have compared the modelled solar response in ozone to observation-based data sets that are constructed using satellite instruments such as Total Ozone Mapping Spectrometer (TOMS, Solar Backscatter UltraViolet instrument (SBUV, Stratospheric Aerosol and Gas Experiment (SAGE and Halogen Occultation Experiment (HALOE. A significant difference is seen between simulated and observed ozone during the 1980s, which is probably due to inhomogeneities in the ERA-40 reanalyses. In general, the model with ERA-Interim dynamics shows better agreement with the observations from 1990 onwards than with ERA-40. Overall both standard model simulations are partially able to simulate a "double peak"-structured ozone solar response with a minimum around 30 km, and these are in better agreement with HALOE than SAGE-corrected SBUV (SBUV/SAGE or SAGE-based data sets. In the tropical lower stratosphere (TLS, the modelled solar response with time-varying aerosols is amplified through aliasing with a volcanic signal, as the model overestimates ozone loss during high aerosol loading years. However, the modelled solar response with fixed dynamics and constant aerosols shows a positive signal which is in better agreement with SBUV/SAGE and SAGE-based data sets in the TLS. Our model simulations suggests that photochemistry contributes to the ozone solar response in this region. The largest model-observation differences occur in the upper stratosphere where SBUV/SAGE and SAGE-based data show a significant (up to 4% solar response whereas the standard model and HALOE do not. This is partly due to a positive solar response in the ECMWF upper stratospheric temperatures which

  7. Consistent simulation of bromine chemistry from the marine boundary layer to the stratosphere, Part I: model description, sea salt aerosols and pH

    Directory of Open Access Journals (Sweden)

    A. Kerkweg

    2008-04-01

    Full Text Available This is the first article of a series presenting a detailed analysis of bromine chemistry simulated with the atmospheric chemistry general circulation model ECHAM5/MESSy. Release from sea salt is an important bromine source, hence the model explicitly calculates aerosol chemistry and phase partitioning for coarse mode aerosol particles. Many processes including chemical reaction rates are influenced by the particle size distribution, and aerosol associated water strongly affects the aerosol pH. Knowledge of the aerosol pH is important as it determines the aerosol chemistry, e.g., the efficiency of sulphur oxidation and bromine release. Here, we focus on the simulated sea salt aerosol size distribution and the coarse mode aerosol pH.

    A comparison with available field data shows that the simulated aerosol distributions agree reasonably well within the range of measurements. In spite of the small number of aerosol pH measurements and the uncertainty in its experimental determination, the simulated aerosol pH compares well with the observations. The aerosol pH ranges from alkaline aerosol in areas of strong production down to pH values of 1 over regions of medium sea salt production and high levels of gas phase acids, mostly polluted regions over the oceans in the northern hemisphere.

  8. Consistent simulation of bromine chemistry from the marine boundary layer to the stratosphere – Part 1: Model description, sea salt aerosols and pH

    Directory of Open Access Journals (Sweden)

    A. Kerkweg

    2008-10-01

    Full Text Available This is the first article of a series presenting a detailed analysis of bromine chemistry simulated with the atmospheric chemistry general circulation model ECHAM5/MESSy. Release from sea salt is an important bromine source, hence the model explicitly calculates aerosol chemistry and phase partitioning for coarse mode aerosol particles. Many processes including chemical reaction rates are influenced by the particle size distribution, and aerosol associated water strongly affects the aerosol pH. Knowledge of the aerosol pH is important as it determines the aerosol chemistry, e.g., the efficiency of sulphur oxidation and bromine release. Here, we focus on the simulated sea salt aerosol size distribution and the coarse mode aerosol pH.

    A comparison with available field data shows that the simulated aerosol distributions agree reasonably well within the range of measurements. In spite of the small number of aerosol pH measurements and the uncertainty in its experimental determination, the simulated aerosol pH compares well with the observations. The aerosol pH ranges from alkaline aerosol in areas of strong production down to pH-values of 1 over regions of medium sea salt production and high levels of gas phase acids, mostly polluted regions over the oceans in the Northern Hemisphere.

  9. Determination of cloud and aerosol layers using CALIPSO and image processing

    Science.gov (United States)

    Alias, A. N.; MatJafri, M. Z.; Lim, H. S.; Abdullah, K.; Saleh, N. Mohd.

    2008-10-01

    The height of cloud and aerosol layers in the atmosphere is believed to affect climate change and air pollution because both of them have important direct effects on the radiation balance of the earth. In this paper, we study the ability of Cloud Aerosol LIDAR and Infrared Pathfinder Satellite Observation (CALIPSO) data to detect, locate and distinguish between cloud and aerosol layers in the atmosphere over Peninsula Malaysia. We also used image processing technique to differentiate between cloud and aerosol layers from the CALIPSO images. The cloud and aerosol layers mostly are seen at troposphere (>10 km) and lower stratosphere (>15km). The results shows that CALIPSO can be used to determine cloud and aerosol layers and image processing technique has successfully distinguished them in the atmosphere.

  10. Effect of Terrestrial and Marine Organic Aerosol on Regional and Global Climate: Model Development, Application, and Verification with Satellite Data

    Energy Technology Data Exchange (ETDEWEB)

    Meskhidze, Nicholas; Zhang, Yang; Kamykowski, Daniel

    2012-03-28

    In this DOE project the improvements to parameterization of marine primary organic matter (POM) emissions, hygroscopic properties of marine POM, marine isoprene derived secondary organic aerosol (SOA) emissions, surfactant effects, new cloud droplet activation parameterization have been implemented into Community Atmosphere Model (CAM 5.0), with a seven mode aerosol module from the Pacific Northwest National Laboratory (PNNL)'s Modal Aerosol Model (MAM7). The effects of marine aerosols derived from sea spray and ocean emitted biogenic volatile organic compounds (BVOCs) on microphysical properties of clouds were explored by conducting 10 year CAM5.0-MAM7 model simulations at a grid resolution 1.9° by 2.5° with 30 vertical layers. Model-predicted relationship between ocean physical and biological systems and the abundance of CCN in remote marine atmosphere was compared to data from the A-Train satellites (MODIS, CALIPSO, AMSR-E). Model simulations show that on average, primary and secondary organic aerosol emissions from the ocean can yield up to 20% increase in Cloud Condensation Nuclei (CCN) at 0.2% Supersaturation, and up to 5% increases in droplet number concentration of global maritime shallow clouds. Marine organics were treated as internally or externally mixed with sea salt. Changes associated with cloud properties reduced (absolute value) the model-predicted short wave cloud forcing from -1.35 Wm-2 to -0.25 Wm-2. By using different emission scenarios, and droplet activation parameterizations, this study suggests that addition of marine primary aerosols and biologically generated reactive gases makes an important difference in radiative forcing assessments. All baseline and sensitivity simulations for 2001 and 2050 using global-through-urban WRF/Chem (GU-WRF) were completed. The main objective of these simulations was to evaluate the capability of GU-WRF for an accurate representation of the global atmosphere by exploring the most accurate

  11. All sky imaging observations in visible and infrared waveband for validation of satellite cloud and aerosol products

    Science.gov (United States)

    Lu, Daren; Huo, Juan; Zhang, W.; Liu, J.

    A series of satellite sensors in visible and infrared wavelengths have been successfully operated on board a number of research satellites, e.g. NOAA/AVHRR, the MODIS onboard Terra and Aqua, etc. A number of cloud and aerosol products are produced and released in recent years. However, the validation of the product quality and accuracy are still a challenge to the atmospheric remote sensing community. In this paper, we suggest a ground based validation scheme for satellite-derived cloud and aerosol products by using combined visible and thermal infrared all sky imaging observations as well as surface meteorological observations. In the scheme, a visible digital camera with a fish-eye lens is used to continuously monitor the all sky with the view angle greater than 180 deg. The digital camera system is calibrated for both its geometry and radiance (broad blue, green, and red band) so as to a retrieval method can be used to detect the clear and cloudy sky spatial distribution and their temporal variations. A calibrated scanning thermal infrared thermometer is used to monitor the all sky brightness temperature distribution. An algorithm is developed to detect the clear and cloudy sky as well as cloud base height by using sky brightness distribution and surface temperature and humidity as input. Based on these composite retrieval of clear and cloudy sky distribution, it can be used to validate the satellite retrievals in the sense of real-simultaneous comparison and statistics, respectively. What will be presented in this talk include the results of the field observations and comparisons completed in Beijing (40 deg N, 116.5 deg E) in year 2003 and 2004. This work is supported by NSFC grant No. 4002700, and MOST grant No 2001CCA02200

  12. Four dimensional variational data assimilation of species-resolved satellite-retrieved aerosol optical thickness

    Science.gov (United States)

    Nieradzik, Lars Peter; Elbern, Hendrik

    2010-05-01

    Aerosols play an increasingly important role in atmospheric modelling. They have a strong influence on the radiative transfer balance and a significant impact on human health. Their origin is various and so are its effects. Most of the measurement sites in Europe only account for an integrated aerosol load PMx (Particulate Matter of less than x μm in diameter) which does not give any qualitative information on the composition of the aerosol. Since very different constituents like mineral dust derived from desert storms and sea salt contribute to PMx it is necessary to make aerosol forcasts not only of load, but also type resolved. The source of information chosen for this study is the aerosol retrieval system SYNAER (SYNergetic AErosol Retrieval) from DLR-DFD that retrieves BLAOT (Boundary Layer Aerosol Optical Thickness) making use of both AATSR/SCIAMACHY and AVHRR/GOME-2 data respectively. Its strengths are a large spatial coverage, near real-time availability, and the classification of five intrinsic aerosol species, namely water-solubles, water-insolubles, soot, sea salt, and mineral dust which are furthermore size resolved in terms of modes. A widely known technique to enhance forecast skills of CTMs (Chemistry-Transport-Models) by ingesting in-situ and, especially, remote-sensing measurements is the method of four dimensional variational data assimilation (4Dvar). The EURAD-IM (EURopean Air pollution Dispersion - Inverse Model), containing a full adjoint gas-phase model, has been expanded with an adjoint of the MADE (Modal Aerosol Dynamics model for Europe) to optimise initial and boundary values for aerosols using 4Dvar. A forward and an adjoint radiative transfer model is driven by the EURAD-IM as mapping between BLAOT and internal aerosol species. Furthermore, its condensation scheme has been bypassed by an HDMR (High-Dimensional-Model-Representation) to ensure differentiability, and a time saving online NMC-module for the generation of the background

  13. Impact of aerosols on marine cloud microphysics over the Indian Ocean using satellite data.

    Science.gov (United States)

    Rao, Sofiya; Dey, Sagnik

    2017-04-01

    Aerosol-cloud interaction is the one of the least understood and largest sources of uncertainty in quantifying climate forcing. Despite progress, the problem remains unresolved because of the buffering effect of meteorology and therefore it is suggested to separate the meteorological forcing from aerosol forcing focusing on different cloud types (Stevens and Feingold 2009). However, most of the previous studies on aerosol-cloud interaction over the Indian Ocean (including INDOEX) are limited to either one particular season or short period. We examine relationships between aerosol and cloud parameters using MODIS data sets for 15 years (2000-2015) period over Indian Ocean. We separated the meteorological forcing from aerosol forcing. In both the Arabian Sea (AS) and Bay of Bengal (BOB), the meteorological forcing is largest in the monsoon. In all the four seasons, cloud microphysical properties are more sensitive to aerosol optical depth (AOD) over the AS compared to BOB. Further analysis reveals presence of semi-direct effect in the winter season. Influence of aerosols on liquid water path (LWP) - cloud effective radius (Reff) relation is quantified. Cloud albedo (Rc) dependency on LWP and Reff is examined in view of changing aerosol load. Cloud drop growth is facilitated in presence of high moisture content. This is evident from the fact that Reff is found to broadly increase with an increase in LWP in every season over Arabian Sea as well as over Bay of Bengal. It is also noted that Reff is larger across a wide range of LWP in 'clean' condition (AOD polluted' condition (0.2 polluted' condition and (AOD > 0.4). This clearly demonstrate that in more polluted conditions, growth of cloud drops are restricted. This is the evidence of classic aerosol indirect effect. However, we notice a saturation in the decrease in Reff with an increase in AOD beyond 0.4. The results provide robust observational evidence of aerosol-cloud interaction in the Indian Ocean region that

  14. Coupled Chemistry Climate Model Simulations of Stratospheric Temperature for the Recent Past

    Science.gov (United States)

    Austin, J.

    2007-12-01

    Temperature results for the recent past from multi-decadal simulations of eleven coupled chemistry climate models are analysed using multi-linear regression including a trend, solar cycle and volcanic aerosol terms. The climatology of the models since 1980 is in good agreement with observations for the troposphere but diverge from each other and from observations in the stratosphere. Overall, the models agree better with observations than previous assessments. As a function of latitude and pressure, the simulated trends vary substantially from model to model, although all models show several consistent features. These include statistically significant cooling trends from about the lower stratosphere upwards in the low and middle latitudes. Several models have statistically significant cooling in the lower stratosphere over the polar region. The temporal variation in the global average temperature in the lower stratosphere indicates a clear increase during volcanic eruptions, superimposed on an overall cooling. The model responses to the volcanic aerosol varies by about a factor of two with several models substantially overpredicting the observed response during the 1980s and 1990s. The globally averaged temperature simulated by the models is generally in agreement with corrected satellite observations over much of their range. Model trend comparisons are also shown for the polar spring and illlustrate even larger inter-model differences. These differences are caused by different simulations of trends in planetary waves and ozone amounts, and illustrate the challenge of predicting ozone recovery in polar regions.

  15. Aerosol data assimilation using data from Himawari‐8, a next‐generation geostationary meteorological satellite

    National Research Council Canada - National Science Library

    Yumimoto, K; Nagao, T.M; Kikuchi, M; Sekiyama, T.T; Murakami, H; Tanaka, T.Y; Ogi, A; Irie, H; Khatri, P; Okumura, H; Arai, K; Morino, I; Uchino, O; Maki, T

    2016-01-01

    ...‐8 data to aerosol data assimilation. Validation of the assimilation experiment by comparison with independent observations demonstrated successful modeling of continental pollution that was not predicted by simulation without...

  16. Stratospheric solar geoengineering without ozone loss

    Science.gov (United States)

    Keith, David W.; Weisenstein, Debra K.; Dykema, John A.; Keutsch, Frank N.

    2016-12-01

    Injecting sulfate aerosol into the stratosphere, the most frequently analyzed proposal for solar geoengineering, may reduce some climate risks, but it would also entail new risks, including ozone loss and heating of the lower tropical stratosphere, which, in turn, would increase water vapor concentration causing additional ozone loss and surface warming. We propose a method for stratospheric aerosol climate modification that uses a solid aerosol composed of alkaline metal salts that will convert hydrogen halides and nitric and sulfuric acids into stable salts to enable stratospheric geoengineering while reducing or reversing ozone depletion. Rather than minimizing reactive effects by reducing surface area using high refractive index materials, this method tailors the chemical reactivity. Specifically, we calculate that injection of calcite (CaCO3) aerosol particles might reduce net radiative forcing while simultaneously increasing column ozone toward its preanthropogenic baseline. A radiative forcing of ‑1 Wṡm‑2, for example, might be achieved with a simultaneous 3.8% increase in column ozone using 2.1 Tgṡy‑1 of 275-nm radius calcite aerosol. Moreover, the radiative heating of the lower stratosphere would be roughly 10-fold less than if that same radiative forcing had been produced using sulfate aerosol. Although solar geoengineering cannot substitute for emissions cuts, it may supplement them by reducing some of the risks of climate change. Further research on this and similar methods could lead to reductions in risks and improved efficacy of solar geoengineering methods.

  17. Impact of absorbing aerosol deposition on snow albedo reduction over the southern Tibetan plateau based on satellite observations

    Science.gov (United States)

    Lee, Wei-Liang; Liou, K. N.; He, Cenlin; Liang, Hsin-Chien; Wang, Tai-Chi; Li, Qinbin; Liu, Zhenxin; Yue, Qing

    2017-08-01

    We investigate the snow albedo variation in spring over the southern Tibetan Plateau induced by the deposition of light-absorbing aerosols using remote sensing data from moderate resolution imaging spectroradiometer (MODIS) aboard Terra satellite during 2001-2012. We have selected pixels with 100 % snow cover for the entire period in March and April to avoid albedo contamination by other types of land surfaces. A model simulation using GEOS-Chem shows that aerosol optical depth (AOD) is a good indicator for black carbon and dust deposition on snow over the southern Tibetan Plateau. The monthly means of satellite-retrieved land surface temperature (LST) and AOD over 100 % snow-covered pixels during the 12 years are used in multiple linear regression analysis to derive the empirical relationship between snow albedo and these variables. Along with the LST effect, AOD is shown to be an important factor contributing to snow albedo reduction. We illustrate through statistical analysis that a 1-K increase in LST and a 0.1 increase in AOD indicate decreases in snow albedo by 0.75 and 2.1 % in the southern Tibetan Plateau, corresponding to local shortwave radiative forcing of 1.5 and 4.2 W m-2, respectively.

  18. Improvement of Aerosol Optical Depth Retrieval over Hong Kong from a Geostationary Meteorological Satellite Using Critical Reflectance with Background Optical Depth Correction

    Science.gov (United States)

    Kim, Mijin; Kim, Jhoon; Wong, Man Sing; Yoon, Jongmin; Lee, Jaehwa; Wu, Dong L.; Chan, P.W.; Nichol, Janet E.; Chung, Chu-Yong; Ou, Mi-Lim

    2014-01-01

    Despite continuous efforts to retrieve aerosol optical depth (AOD) using a conventional 5-channelmeteorological imager in geostationary orbit, the accuracy in urban areas has been poorer than other areas primarily due to complex urban surface properties and mixed aerosol types from different emission sources. The two largest error sources in aerosol retrieval have been aerosol type selection and surface reflectance. In selecting the aerosol type from a single visible channel, the season-dependent aerosol optical properties were adopted from longterm measurements of Aerosol Robotic Network (AERONET) sun-photometers. With the aerosol optical properties obtained fromthe AERONET inversion data, look-up tableswere calculated by using a radiative transfer code: the Second Simulation of the Satellite Signal in the Solar Spectrum (6S). Surface reflectance was estimated using the clear sky composite method, awidely used technique for geostationary retrievals. Over East Asia, the AOD retrieved from the Meteorological Imager showed good agreement, although the values were affected by cloud contamination errors. However, the conventional retrieval of the AOD over Hong Kong was largely underestimated due to the lack of information on the aerosol type and surface properties. To detect spatial and temporal variation of aerosol type over the area, the critical reflectance method, a technique to retrieve single scattering albedo (SSA), was applied. Additionally, the background aerosol effect was corrected to improve the accuracy of the surface reflectance over Hong Kong. The AOD retrieved froma modified algorithmwas compared to the collocated data measured by AERONET in Hong Kong. The comparison showed that the new aerosol type selection using the critical reflectance and the corrected surface reflectance significantly improved the accuracy of AODs in Hong Kong areas,with a correlation coefficient increase from0.65 to 0.76 and a regression line change from tMI [basic algorithm] = 0

  19. Solar energy assessment in the Alpine area: satellite data and ground instruments integration for studying the radiative forcing of aerosols.

    Science.gov (United States)

    Castelli, M.; Petitta, M.; Emili, E.

    2012-04-01

    The primary objective of this work is to purpose an approach for estimating the effect of aerosols on surface incoming shortwave radiation (SIS) in the Alpine region, which is based on the integration of different instruments: we develop a GIS model, whose output is corrected by monthly atmospheric coefficients, and then we progressively add details by daily updated atmospheric information. The assessment of solar energy availability at the earth's surface over a specific geographic area is crucial for planning photovoltaic panels installation. When modeling SIS with GIS instruments or retrieving it from satellites measurements, we have to account for terrain shadowing and atmospheric extinction, both of which are difficult to describe in the Alpine area, because of the topographic complexity and the local atmospheric circulation influence on the atmospheric composition. While advanced methods were developed to carefully describe the effect of topography, the atmospheric attenuation was considered so far only through monthly turbidity values, and the question remains whether it be possible to develop a time-effective routine to model the atmospheric effect on SIS at daily scale. As a first step we produced a WebGIS for the town of Bressanone, Italy, showing a classification of the roofs of the buildings according to the yearly amount of global irradiance. Furthermore we provide the annual electricity production based on the efficiency of the most common PV technologies. At this stage clear sky irradiance was computed with a GIS based model, and afterwards monthly correction coefficients were applied to add real sky conditions to the merely geometrical computations, which were obtained from 20 years of measurement collected by the pyranometer in the closest meteorological station. As a second step we investigate the influence of aerosol optical properties on SIS by running the radiative transfer model libRadtran by using as input the aerosol model defined for the

  20. Aerosol microphysics simulations of the Mt.~Pinatubo eruption with the UM-UKCA composition-climate model

    Science.gov (United States)

    Dhomse, S. S.; Emmerson, K. M.; Mann, G. W.; Bellouin, N.; Carslaw, K. S.; Chipperfield, M. P.; Hommel, R.; Abraham, N. L.; Telford, P.; Braesicke, P.; Dalvi, M.; Johnson, C. E.; O'Connor, F.; Morgenstern, O.; Pyle, J. A.; Deshler, T.; Zawodny, J. M.; Thomason, L. W.

    2014-10-01

    We use a stratosphere-troposphere composition-climate model with interactive sulfur chemistry and aerosol microphysics, to investigate the effect of the 1991 Mount Pinatubo eruption on stratospheric aerosol properties. Satellite measurements indicate that shortly after the eruption, between 14 and 23 Tg of SO2 (7 to 11.5 Tg of sulfur) was present in the tropical stratosphere. Best estimates of the peak global stratospheric aerosol burden are in the range 19 to 26 Tg, or 3.7 to 6.7 Tg of sulfur assuming a composition of between 59 and 77 % H2SO4. In light of this large uncertainty range, we performed two main simulations with 10 and 20 Tg of SO2 injected into the tropical lower stratosphere. Simulated stratospheric aerosol properties through the 1991 to 1995 period are compared against a range of available satellite and in situ measurements. Stratospheric aerosol optical depth (sAOD) and effective radius from both simulations show good qualitative agreement with the observations, with the timing of peak sAOD and decay timescale matching well with the observations in the tropics and mid-latitudes. However, injecting 20 Tg gives a factor of 2 too high stratospheric aerosol mass burden compared to the satellite data, with consequent strong high biases in simulated sAOD and surface area density, with the 10 Tg injection in much better agreement. Our model cannot explain the large fraction of the injected sulfur that the satellite-derived SO2 and aerosol burdens indicate was removed within the first few months after the eruption. We suggest that either there is an additional alternative loss pathway for the SO2 not included in our model (e.g. via accommodation into ash or ice in the volcanic cloud) or that a larger proportion of the injected sulfur was removed via cross-tropopause transport than in our simulations. We also critically evaluate the simulated evolution of the particle size distribution, comparing in detail to balloon-borne optical particle counter (OPC

  1. Merging aerosol optical depth data from multiple satellite missions to view agricultural biomass burning in Central and East China

    Directory of Open Access Journals (Sweden)

    Y. Xue

    2012-04-01

    Full Text Available Agricultural biomass burning (ABB in Central and East China occurs every year from May to October and peaks in June. The biomass burning event in June 2007 was very strong. During the period from 26 May to 16 June 2007, ABB occurred mainly in Anhui, Henan, Jiangsu and Shandong provinces. A comprehensive set of aerosol optical depth (AOD data, produced by a merger of AOD product data from the Moderate Resolution Imaging Spectroradiometer (MODIS and the Multiangle Imaging Spectroradiometer (MIRS, is used to study the spatial and temporal distribution of agricultural biomass aerosols in Central and East China combining with ground observations from both AErosol RObotic NETwork (AERONET and China Aerosol Remote Sensing NETwork (CARSNET measurements. We compared merged AOD data with single-sensor single-algorithm AOD data (MODIS Dark Target AOD data, MODIS Deep Blue AOD data, SRAP-MODIS AOD data and MISR AOD data. In this comparison, we found merged AOD products can improve the quality of AOD products from single-sensor single-algorithm data sets by expanding the spatial coverage of the study area and keeping the statistical confidence in AOD parameters. There existed high correlation (0.8479 between the merged AOD data and AERONET measurements. Our merged AOD data make use of synergetic information conveyed in all of the available satellite data. The merged AOD data were used for the analysis of the biomass burning event from 26 May to 16 June 2007 together with meteorological data. The merged AOD products and the ground observations from China suggest that biomass burning in Central and East China has had great impact on AOD over China. Influenced by this ABB, the highest AOD value in Beijing on 12 June 2007 reached 5.71.

  2. Merging aerosol optical depth data from multiple satellite missions to view agricultural biomass burning in Central and East China

    Science.gov (United States)

    Xue, Y.; Xu, H.; Mei, L.; Guang, J.; Guo, J.; Li, Y.; Hou, T.; Li, C.; Yang, L.; He, X.

    2012-04-01

    Agricultural biomass burning (ABB) in Central and East China occurs every year from May to October and peaks in June. The biomass burning event in June 2007 was very strong. During the period from 26 May to 16 June 2007, ABB occurred mainly in Anhui, Henan, Jiangsu and Shandong provinces. A comprehensive set of aerosol optical depth (AOD) data, produced by a merger of AOD product data from the Moderate Resolution Imaging Spectroradiometer (MODIS) and the Multiangle Imaging Spectroradiometer (MIRS), is used to study the spatial and temporal distribution of agricultural biomass aerosols in Central and East China combining with ground observations from both AErosol RObotic NETwork (AERONET) and China Aerosol Remote Sensing NETwork (CARSNET) measurements. We compared merged AOD data with single-sensor single-algorithm AOD data (MODIS Dark Target AOD data, MODIS Deep Blue AOD data, SRAP-MODIS AOD data and MISR AOD data). In this comparison, we found merged AOD products can improve the quality of AOD products from single-sensor single-algorithm data sets by expanding the spatial coverage of the study area and keeping the statistical confidence in AOD parameters. There existed high correlation (0.8479) between the merged AOD data and AERONET measurements. Our merged AOD data make use of synergetic information conveyed in all of the available satellite data. The merged AOD data were used for the analysis of the biomass burning event from 26 May to 16 June 2007 together with meteorological data. The merged AOD products and the ground observations from China suggest that biomass burning in Central and East China has had great impact on AOD over China. Influenced by this ABB, the highest AOD value in Beijing on 12 June 2007 reached 5.71.

  3. In-situ BrO measurements in the upper troposphere / lower stratosphere. Validation of the ENVISAT satellite measurements and photochemical model studies

    Energy Technology Data Exchange (ETDEWEB)

    Hrechanyy, S.

    2007-04-15

    Inorganic bromine species form the second most important halogen family affecting stratospheric ozone (WMO, 2003). Although the stratospheric bromine mixing ratio is about two orders of magnitude lower than the chlorine one, bromine has much higher ozone depleting potential (factor of about 45) compared to chlorine. This study reports and discusses atmospheric bromine monoxide, BrO, measurements in the altitude range 15-30 km performed by the balloon-borne instrument TRIPLE and aircraft instrument HALOX employing the chemical conversion resonance fluorescence technique, which is the only proven in-situ technique for the measurements of BrO. 57 HALOX flights have been performed in the frame of five field campaigns ranging from the Arctic to tropics. Three TRIPLE flights were carried out at high and mid latitudes in the frame of the SCIAMACHY (SCanning Imaging Absorption spectroMeter for Atmospheric CHartographY) validation. Calibration, consistency checks, data analysis, and error assessment for the in-situ measurements are described. The balloon measurements have yielded vertical profiles of BrO between 15 and 30 km altitude at northern mid- and at arctic latitudes. From the aircraft measurements a meridional BrO distribution from tropical to the arctic latitudes between 15 and 20 km altitude was obtained. In order to check the reliability of the bromine chemistry in the CLaMS model the BrO profile measured by TRIPLE on June 9, 2003 in Arctic spring/summer conditions was compared to a simulated BrO profile. For the simulation the model was initialized with appropriate satellite and balloon measurements and with a total stratospheric bromine of 18.4 pptv. Very good agreement between the TRIPLE measurements and model results was found. Measurements of BrO in the tropical tropopause layer (TTL) are well suited to investigate the contribution of very short-lived bromine species (VSLS) to the inorganic bromine, Bry. Since tropical HALOX BrO measurements from TROCCINOX

  4. Evaluation of Aerosol Pollution Determination From MODIS Satellite Retrievals for Semi-Arid Reno, NV, USA with In-Situ Measurements

    Science.gov (United States)

    Loria-Salazar, S. Marcela

    The aim of the present work is to carry out a detailed analysis of ground and columnar aerosol properties obtained by in-situ Photoacoustic and Integrated Nephelometer (PIN), Cimel CE-318 sunphotometer and MODIS instrument onboard Aqua and Terra satellites, for semi-arid Reno, Nevada, USA in the local summer months of 2012. Satellite determination of local aerosol pollution is desirable because of the potential for broad spatial and temporal coverage. However, retrieval of quantitative measures of air pollution such as Aerosol Optical Depth (AOD) from satellite measurements is challenging because of the underlying surface albedo being heterogeneous in space and time. Therefore, comparisons of satellite retrievals with measurements from ground-based sun photometers are crucial for validation, testing, and further development of instruments and retrieval algorithms. Ground-based sunphotometry and in-situ ground observations show that seasonal weather changes and fire plumes have great influence on the atmosphere aerosol optics. The Apparent Optical Height (AOH) follows the shape of the development of the Convective Boundary Layer (CBL) when fire conditions were not present. However, significant fine particle optical depth was inferred beyond the CBL thereby complicating the use of remote sensing measurements for near-ground aerosol pollution measurements. A meteorological analysis was performed to help diagnose the nature of the aerosols above Reno. The calculation of a Zephyr index and back trajectory analysis demonstrated that a local circulation often induces aerosol transport from Northern CA over the Sierra Nevada Mountains that doubles the Aerosol Optical Depth (AOD) at 500 nm. Sunphotometer measurements were used as a `ground truth' for satellite retrievals to evaluate the current state of the science retrievals in this challenging location. Satellite retrieved for AOD showed the presence of wild fires in Northern CA during August. AOD retrieved using the

  5. Diurnal variation of stratospheric and lower mesospheric HOCl, ClO and HO2 at the equator: comparison of 1-D model calculations with measurements by satellite instruments

    Directory of Open Access Journals (Sweden)

    M. Khosravi

    2013-08-01

    Full Text Available The diurnal variation of HOCl and the related species ClO, HO2 and HCl measured by satellites has been compared with the results of a one-dimensional photochemical model. The study compares the data from various limb-viewing instruments with model simulations from the middle stratosphere to the lower mesosphere. Data from three sub-millimetre instruments and two infrared spectrometers are used, namely from the Sub-Millimetre Radiometer (SMR on board Odin, the Microwave Limb Sounder (MLS on board Aura, the Superconducting Submillimeter-wave Limb-Emission Sounder (SMILES on the International Space Station, the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS on board ENVISAT, and the Atmospheric Chemistry Experiment Fourier Transform Spectrometer (ACE-FTS on board SCISAT. Inter-comparison of the measurements from instruments on sun-synchronous satellites (SMR, MLS, MIPAS and measurements from solar occultation instruments (ACE-FTS is challenging since the measurements correspond to different solar zenith angles (or local times. However, using a model which covers all solar zenith angles and data from the SMILES instrument which measured at all local times over a period of several months provides the possibility to verify the model and to indirectly compare the diurnally variable species. The satellite data were averaged for latitudes of 20° S to 20° N for the SMILES observation period from November 2009 to April 2010 and were compared at three altitudes: 35, 45 and 55 km. Besides presenting the SMILES data, the study also shows a first comparison of the latest MLS data (version 3.3 of HOCl, ClO, and HO2 with other satellite observations, as well as a first evaluation of HO2 observations made by Odin/SMR. The MISU-1D model has been carefully initialised and run for conditions and locations of the observations. The diurnal cycle features for the species investigated here are generally well reproduced by the model. The satellite

  6. Spatio-temporal variability of satellite derived aerosol optical thickness and ground measurements over East China

    Science.gov (United States)

    Meng, Fei; Shi, Tongguang

    2016-04-01

    Two-year records of Visible Infrared Imaging Radiometer Suite (VIIRS) Intermediate Product (IP) data on the aerosol optical thickness (AOT) at 550 nm were evaluated by comparing them with sun-sky radiometer measurements from the Chinese sun hazemeter network (CSHNET) and the aerosol robotic network (AERONET). The monthly and seasonal variations in the aerosol optical properties over eastern China were then investigated using collocated VIIRS IP data and CSHNET and AERONET measurements.Results show that the performances of the current VIIRS IP AOT retrievals at the provisional stage were consistent with ground measurements. Similar characteristics of seasonal and monthly variations were found among the measurements, though the observational methodologies were different, showing maxima in the summer and spring and minima in the winter and autumn.

  7. The ASSET intercomparison of stratosphere and lower mesosphere humidity analyses

    Directory of Open Access Journals (Sweden)

    H. E. Thornton

    2009-02-01

    Full Text Available This paper presents results from the first detailed intercomparison of stratosphere-lower mesosphere water vapour analyses; it builds on earlier results from the EU funded framework V "Assimilation of ENVISAT Data" (ASSET project. Stratospheric water vapour plays an important role in many key atmospheric processes and therefore an improved understanding of its daily variability is desirable. With the availability of high resolution, good quality Michelson Interferometer for Passive Atmospheric Sounding (MIPAS water vapour profiles, the ability of four different atmospheric models to assimilate these data is tested. MIPAS data have been assimilated over September 2003 into the models of the European Centre for Medium Range Weather Forecasts (ECMWF, the Belgian Institute for Space and Aeronomy (BIRA-IASB, the French Service d'Aéronomie (SA-IPSL and the UK Met Office. The resultant middle atmosphere humidity analyses are compared against independent satellite data from the Halogen Occultation Experiment (HALOE, the Polar Ozone and Aerosol Measurement (POAM III and the Stratospheric Aerosol and Gas Experiment (SAGE II. The MIPAS water vapour profiles are generally well assimilated in the ECMWF, BIRA-IASB and SA systems, producing stratosphere-mesosphere water vapour fields where the main features compare favourably with the independent observations. However, the models are less capable of assimilating the MIPAS data where water vapour values are locally extreme or in regions of strong humidity gradients, such as the southern hemisphere lower stratosphere polar vortex. Differences in the analyses can be attributed to the choice of humidity control variable, how the background error covariance matrix is generated, the model resolution and its complexity, the degree of quality control of the observations and the use of observations near the model boundaries. Due to the poor performance of the Met Office analyses the results are not included in

  8. Initial approach in biomass burning aerosol transport tracking with CALIPSO and MODIS satellites, sunphotometer, and a backscatter lidar system in Brazil

    Science.gov (United States)

    Landulfo, E.; Lopes, F. J. S.

    2009-09-01

    Nowadays there is an increasing concern about the direct and indirect influence of the aerosols in the Earth's radiative budget. Aerosols from biomass burning activities have been identified as a significant radiative forcing agent. A significant concentration quantity of aerosol particles observed in the atmosphere can be associated with intense anthropogenic biomass burning activity. The CALIPSO satellite and ground-based Lidar systems are indispensable to provide the vertical structure and optical properties of aerosol and clouds on global and local scale, respectively. The Brazilian mid-western region is one of the biggest producers of biomass burning in the whole continent. Aerosols from biomass burning can be transported to distances of hundreds or thousands of kilometers. It has been developed a computational routine to map the CALIPSO overpasses over the whole country in order to retrieve the total coverage taking special attention in the Brazilian AERONET sites. In this context, the measured data from AERONET, CALIPSO and MODIS Satellite and the MSP-Lidar system from Instituto de Pesquisas Energéticas e Nucleares (IPEN) can be used to map the aerosols biomass burning plumes transported from the mid-western to the southeastern region. In total 5 sites were chosen spanning from 0 to 23 South latitude and 46 to 60 West in longitude in coverage during 2007 and we were able to identify such transports during the months of August and September.

  9. Effects of agriculture crop residue burning on aerosol properties and long-range transport over northern India: A study using satellite data and model simulations

    Science.gov (United States)

    Vijayakumar, K.; Safai, P. D.; Devara, P. C. S.; Rao, S. Vijaya Bhaskara; Jayasankar, C. K.

    2016-09-01

    Agriculture crop residue burning in the tropics is a major source of the global atmospheric aerosols and monitoring their long-range transport is an important element in climate change studies. In this paper, we study the effects of agriculture crop residue burning on aerosol properties and long-range transport over northern India during a smoke event that occurred between 09 and 17 November 2013, with the help of satellite measurements and model simulation data. Satellite data observations on aerosol properties suggested transport of particles from agriculture crop residue burning in Indo-Gangetic Plains (IGP) over large regions. Additionally, ECMWF winds at 850 hPa have been used to trace the source, path and spatial extent of smoke events. Most of the smoke aerosols, during the study period, travel from a west-to-east pathway from the source-to-sink region. Furthermore, aerosol vertical profiles from CALIPSO show a layer of thick smoke extending from surface to an altitude of about 3 km. Smoke aerosols emitted from biomass burning activity from Punjab have been found to be a major contributor to the deterioration of local air quality over the NE Indian region due to their long range transport.

  10. Retrieval of stratospheric ozone profiles from OMPS measurements in limb viewing geometry

    Science.gov (United States)

    Arosio, Carlo; Rozanov, Alexei; Eichmann, Kai-Uwe; Malinina, Elizaveta; Burrows, John P.; Jaross, Glenn; Bhartia, Pawan K.

    2017-04-01

    Due to its crucial role in the radiative budged of the stratosphere as well as its importance for the mankind as an absorber of biological-damaging UV radiation, a continuous monitoring of the vertical and spatial distribution of the stratospheric ozone has been a priority for the scientific community. At the beginning of 2012 the European ENVISAT satellite, carrying among others ozone-science relevant instruments as GOMOS, MIPAS and SCIAMACHY, ceased its operations: as a consequence, only a few older satellite missions, such as OSIRIS, MLS, ACE-FTS, and SMR have been still operating, contributing to the task of continuous monitoring stratospheric ozone distributions. At the end of 2011, just some months before the end of ENVISAT lifetime, SUOMI-NPP mission carrying OMPS instrument was launched. The OMPS suite enables the study of the vertical distribution of stratospheric ozone by analyzing the intensity of the scattered solar light at UV-VIS wavelengths in limb viewing geometry. The focus of our study is to adapt the algorithm developed at the University of Bremen for the retrieval of stratospheric ozone vertical distributions from SCIAMACHY limb measurements to OMPS limb observations, with the final aim to obtain a continuous data set from both instruments. The retrieval method is based on the optimal estimation technique in a 1D geometry; the settings account for the instrumental design by optimally exploiting different spectral ranges at UV wavelengths as well as in the visible region to retrieve ozone concentrations at different tangent heights. A cloud filter based on the Color Index Ratio is applied and surface albedo is retrieved simultaneously, accounting for stratospheric aerosol. The retrieval results over six months are compared in this poster with the NASA retrieval product and validated using MLS and ozonesondes collocated observations.

  11. Comparisons of LASE, aircraft, and satellite measurements of aerosol optical properties and water vapor during TARFOX

    NARCIS (Netherlands)

    Ferrare, R.; Ismail, S.; Browell, E.; Brackett, V.; Kooi, S.; Clayton, M.; Hobbs, P.V.; Hartley, S.; Veefkind, J.P.; Russell, P.; Livingston, J.; Tanré, D.; Hignett, P.

    2000-01-01

    We examine aerosol extinction and optical thickness from the Lidar Atmospheric Sensing Experiment (LASE), the in situ nephelometer and absorption photometer on the University of Washington C-131A aircraft, and the NASA Ames Airborne Tracking Sun Photometer (AATS-6) on the C-131A measured during the

  12. Comparisons of LASE, aircraft, and satellite measurements of aerosol optical properties and water vapor during TARFOX

    NARCIS (Netherlands)

    Ferrare, R.; Ismail, S.; Browell, E.; Brackett, V.; Kooi, S.; Clayton, M.; Hobbs, P.V.; Hartley, S.; Veefkind, J.P.; Russell, P.; Livingston, J.; Tanré, D.; Hignett, P.

    2000-01-01

    We examine aerosol extinction and optical thickness from the Lidar Atmospheric Sensing Experiment (LASE), the in situ nephelometer and absorption photometer on the University of Washington C-131A aircraft, and the NASA Ames Airborne Tracking Sun Photometer (AATS-6) on the C-131A measured during the

  13. Climate Chemistry Coupling: Ozone Loss Linked to the Unique Dynamical Structure of the Summertime Stratosphere Over the U.S. Using In Situ Aircraft, Satellite and NEXRAD Radar Observations

    Science.gov (United States)

    Anderson, J. G.; Wilmouth, D. M.; Smith, J. B.; Dykema, J. A.; Leroy, S. S.; Koby, T.; Clapp, C.; Bowman, K. P.

    2015-12-01

    A remarkable combination of meteorological and catalytic chemical factors place the summertime lower stratosphere over the U.S. in a unique position at the intersection of climate forcing and potential ozone loss in the stratosphere. The factors that conspire to establish this circumstance engages four independent considerations. First is the occurrence of severe storms in the U.S. Mid-West caused by the intersection of moist airflow from the Gulf of Mexico with airflow from higher latitudes in spring and summer. These storms are characterized by a combination of tornadoes, hail, heavy precipitation and high winds, the frequency and intensity of which are increasing with increased forcing of the climate system by the addition of CO2, CH4, N2O CFCs, and other infrared active species to the atmosphere associated with human activity. Second is the recognition that these severe storms are capable of injecting water vapor deep into the stratosphere over the U.S., with injection depths reaching the altitude of increasing inorganic halogen species formed by the photolytic breakdown of organic chorine and bromine transported into the stratosphere. Third is the recognition that the catalytic conversion of inorganic halogen species to radicals, specifically ClO and BrO, that are the rate limiting catalytic species that destroy ozone, occurs on ubiquitous sulfate-water aerosols wherever and whenever the temperature-water vapor conditions are met. These conditions are met in the Antarctic and Arctic winter vortices by virtue of temperatures below 200K at 5 ppmv water vapor, and in the summertime lower stratosphere over the U.S. by virtue of temperatures between 200 and 205K in combination with convectively injected water vapor concentrations in the range of 8 ppmv or greater. Fourth, is the recognition that the flow pattern of the lower stratosphere over the U.S. in summer is repeatedly under the control of the North American monsoon that forms an anti-cyclonic (clockwise

  14. A~tropical West Pacific OH minimum and implications for stratospheric composition

    Science.gov (United States)

    Rex, M.; Wohltmann, I.; Ridder, T.; Lehmann, R.; Rosenlof, K.; Wennberg, P.; Weisenstein, D.; Notholt, J.; Krüger, K.; Mohr, V.; Tegtmeier, S.

    2014-05-01

    Most of the short-lived biogenic and anthropogenic chemical species that are emitted into the atmosphere break down efficiently by reaction with OH and do not reach the stratosphere. Here we show the existence of a pronounced minimum in the tropospheric column of ozone over the West Pacific, the main source region for stratospheric air, and suggest a corresponding minimum of the tropospheric column of OH. This has the potential to amplify the impact of surface emissions on the stratospheric composition compared to the impact when assuming globally uniform OH conditions. Specifically, the role of emissions of biogenic halogenated species for the stratospheric halogen budget and the role of increasing emissions of SO2 in Southeast Asia or from minor volcanic eruptions for the increasing stratospheric aerosol loading need to be reassessed in light of these findings. This is also important since climate change will further modify OH abundances and emissions of halogenated species. Our study is based on ozone sonde measurements carried out during the TransBrom cruise with the RV Sonne roughly along 140-150° E in October 2009 and corroborating ozone and OH measurements from satellites, aircraft campaigns and FTIR instruments. Model calculations with the GEOS-Chem Chemistry and Transport Model (CTM) and the ATLAS CTM are used to simulate the tropospheric OH distribution over the West Pacific and the transport pathways to the stratosphere. The potential effect of the OH minimum on species transported into the stratosphere is shown via modeling the transport and chemistry of CH2Br2 and SO2.

  15. Solubilities and transport properties of the stratospheric sulphuric acid aerosol: laboratory investigations using extremely thin sulphuric acid films. Final report; Loesungs- und Transporteigenschaften des stratosphaerischen Schwefelsaeureaerosols: Laboruntersuchungen an extrem duennen Schwefelsaeurefilmen. Abschlussbericht

    Energy Technology Data Exchange (ETDEWEB)

    Schurath, U.; Proksch, V.

    2000-04-17

    We have developed a procedure to measure solubilities, diffusion coefficients and rate constants (oxidation; hydrolysis) of trace gases in sulphuric acid at stratospheric temperatures. The results will lead to a better understanding and quantification of heterogeneous reactions in/on sulphuric acid aerosol particles in stratospheric models. Sulphuric acid (19-83 wt-%) is deposited as a thin film (1-3 {mu}m) on the inner surface of a capillary column (i.d. 530 {mu}m). The trace gas under study is injected into the carrier gas which passes through the column. Solubilities, diffusion coefficients and rate constants for the hydrolysis/oxidation of the trace gases in the sulphuric acid film can be deduced from the retention times, shapes and areas of the trace gas peaks which are detected by a mass spectrometer. (orig.) [German] Es wurde ein Verfahren zur Messung von Loeslichkeiten, Diffusionskoeffizienten und Ratenkonstanten (Oxidation; Hydrolyse) von Spurengasen in Schwefelsaeure bei stratosphaerischen Temperaturen entwickelt. Die Messergebnisse dienen dem besseren Verstaendnis und der Quantifizierung von heterogenen Reaktionen am stratosphaerischen Schwefelsaeure-Aerosol in Stratosphaerenmodellen. Die Schwefelsaeure (19-83 Gew.%) befindet sich als duenner Film (1-3 {mu}m) auf der Innenseite einer Kapillarsaeule (ID=530 {mu}m), die von einem Traegergas und dem zu untersuchenden Spurengas durchstroemt wird. Die Kapillarsaeule wird in einem Kryostaten auf 186-263 K gekuehlt. Aus der Ankunftszeit, Form und Flaeche von Spurengaspeaks an einem Massenspektrometer-Detektor koennen Loeslichkeiten und Diffusionskoeffizienten sowie Ratenkonstanten fuer die Hydrolyse/Oxidation von Spurengasen im Schwefelsaeurefilm bestimmt werden. (orig.)

  16. Seasonal variation of near surface black carbon and satellite derived vertical distribution of aerosols over a semi-arid station in India

    Science.gov (United States)

    Kalluri, Raja Obul Reddy; Gugamsetty, Balakrishnaiah; Kotalo, Rama Gopal; Nagireddy, Siva Kumar Reddy; Tandule, Chakradhar Rao; Thotli, Lokeswara Reddy; Shaik, Nazeer Hussain; Maraka, Vasudeva Reddy; Rajuru, Ramakrishna Reddy; Surendran Nair, Suresh Babu

    2017-02-01

    Extensive measurements of aerosol black carbon mass concentration (BC) and vertical profiles of atmospheric aerosols have been carried out using Aethalometer and CALIPSO level - 2 satellite data from December 2012 to November 2014 over a semi-arid station, Anantapur. We found a bimodal distribution in the mass concentrations of BC aerosols on a diurnal scale. A sharp peak was observed during morning rush hours (7:00 to 8:00 LT) almost an hour after the local sunrise. After which, a broad nocturnal peak was found during 21:00 to 22:00 LT. The seasonal mean BC concentrations (Mixed layer height (ML)) were found to be 3.45 ± 1.44 μg/m3 (676 ± 117 m), 2.55 ± 0.85 μg/m3 (1215 ± 190 m), 1.22 ± 0.31 μg/m3 (1134 ± 194 m) and 1.75 ± 0.70 μg/m3 (612 ± 135 m), during the winter, summer, monsoon and post-monsoon respectively. The vertical profiles of aerosol extinction coefficient and back scattering ratio profiles were derived from Cloud Aerosol Lidar and Infrared Pathfinder Satellite Observations (CALIPSO) showed a strong seasonal variation with aerosols mostly confined below 2 km during the post-monsoon and winter seasons whereas in the other two seasons, the aerosol layer expands beyond 6 km. Depolarization ratios (> 0.2) are higher during summer and monsoon at higher altitude regions demonstrate the presence of dust particles, which contribute to the large aerosol extinction at higher levels. These results are further supported by the backward trajectory cluster analysis.

  17. Study on the impact of sudden stratosphere warming in the upper mesosphere-lower thermosphere regions using satellite and HF radar - [Article

    CSIR Research Space (South Africa)

    Mbatha, N

    2010-01-01

    Full Text Available The occurrence of sudden stratospheric warming (SSW) excites disturbances in the mesosphere-lower thermospheric (MLT) wind and temperature. Here, researchers have examined the high frequency (HF) radar wind data from the South African National...

  18. Sources, seasonality, and trends of Southeast US aerosol: an integrated analysis of surface, aircraft, and satellite observations with the GEOS-Chem chemical transport model

    Directory of Open Access Journals (Sweden)

    P. S. Kim

    2015-07-01

    Full Text Available We use an ensemble of surface (EPA CSN, IMPROVE, SEARCH, AERONET, aircraft (SEAC4RS, and satellite (MODIS, MISR observations over the Southeast US during the summer-fall of 2013 to better understand aerosol sources in the region and the relationship between surface particulate matter (PM and aerosol optical depth (AOD. The GEOS-Chem global chemical transport model (CTM with 25 km × 25 km resolution over North America is used as a common platform to interpret measurements of different aerosol variables made at different times and locations. Sulfate and organic aerosol (OA are the main contributors to surface PM2.5 (mass concentration of PM finer than 2.5 μm aerodynamic diameter and AOD over the Southeast US. GEOS-Chem simulation of sulfate requires a missing oxidant, taken here to be stabilized Criegee intermediates, but which could alternatively reflect an unaccounted for heterogeneous process. Biogenic isoprene and monoterpenes account for 60 % of OA, anthropogenic sources for 30 %, and open fires for 10 %. 60 % of total aerosol mass is in the mixed layer below 1.5 km, 20 % in the cloud convective layer at 1.5–3 km, and 20 % in the free troposphere above 3 km. This vertical profile is well captured by GEOS-Chem, arguing against a high-altitude source of OA. The extent of sulfate neutralization (f = [NH4+]/(2[SO42−] + [NO3−] is only 0.5–0.7 mol mol−1 in the observations, despite an excess of ammonia present, which could reflect suppression of ammonia uptake by organic aerosol. This would explain the long-term decline of ammonium aerosol in the Southeast US, paralleling that of sulfate. The vertical profile of aerosol extinction over the Southeast US follows closely that of aerosol mass. GEOS-Chem reproduces observed total column aerosol mass over the Southeast US within 6 %, column aerosol extinction within 16 %, and space-based AOD within 21 %. The large AOD decline observed from summer to winter is driven by sharp declines in both

  19. Stratospheric solar geoengineering without ozone loss?

    Science.gov (United States)

    Keutsch, F. N.; Keith, D.; Weisenstein, D.; Dykema, J. A.

    2016-12-01

    Injecting sulfate aerosol into the stratosphere, a form of solar geoengineering, may reduce some climate risks, but it also entails new risks including ozone loss and heating of the lower tropical stratosphere which in turn increases water vapor concentration causing additional ozone loss and surface warming. Selection of a solid aerosol such as alumina or diamond for geoengineering purposes was found to minimize stratospheric heating for a given shortwave forcing, though ozone depletion via heterogeneous surface activation remains a potential problem. Here we investigate the use of solid aerosols composed of alkaline metal salts whose surfaces would convert halogens, nitric and sulfuric acid into stable salts, reducing the ozone depletion potential of these ubiquitous stratospheric substances and preventing heterogeneous activation on the geoengineering particles. Specifically, injection of calcite (CaCO3) aerosol might reduce net radiative forcing while simultaneously increasing column ozone towards its pre-anthropogenic baseline. A radiative forcing of -1 Wm-2, for example, might be achieved with a simultaneous 3.8% increase in column ozone using 2.1 Tg yr-1 of 275 nm radius calcite aerosol with ten-fold less radiative heating compared to sulfate aerosol. Geoengineering injection of reactive alkali metal salts in combination with another high refractive index material may also enable solar geoengineering with lower risk than with sulfates.

  20. Examination of aerosol distributions and radiative effects over the Bay of Bengal and the Arabian Sea region during ICARB using satellite data and a general circulation model

    Directory of Open Access Journals (Sweden)

    R. Cherian

    2012-02-01

    Full Text Available In this paper we analyse aerosol loading and its direct radiative effects over the Bay of Bengal (BoB and Arabian Sea (AS regions for the Integrated Campaign on Aerosols, gases and Radiation Budget (ICARB undertaken during 2006, using satellite data from the MODerate Resolution Imaging Spectroradiometer (MODIS on board the Terra and Aqua satellites, the Aerosol Index from the Ozone Monitoring Instrument (OMI on board the Aura satellite, and the European-Community Hamburg (ECHAM5.5 general circulation model extended by Hamburg Aerosol Module (HAM. By statistically comparing with large-scale satellite data sets, we firstly show that the aerosol properties measured during the ship-based ICARB campaign and simulated by the model are representative for the BoB and AS regions and the pre-monsoon season. In a second step, the modelled aerosol distributions were evaluated by a comparison with the measurements from the ship-based sunphotometer, and the satellite retrievals during ICARB. It is found that the model broadly reproduces the observed spatial and temporal variability in aerosol optical depth (AOD over BoB and AS regions. However, AOD was systematically underestimated during high-pollution episodes, especially in the BoB leg. We show that this underprediction of AOD is mostly because of the deficiencies in the coarse mode, where the model shows that dust is the dominant component. The analysis of dust AOD along with the OMI Aerosol Index indicate that missing dust transport that results from too low dust emission fluxes over the Thar Desert region in the model caused this deficiency. Thirdly, we analysed the spatio-temporal variability of AOD comparing the ship-based observations to the large-scale satellite observations and simulations. It was found that most of the variability along the track was from geographical patterns, with a minor influence by single events. Aerosol fields were homogeneous enough to yield a good statistical agreement

  1. Long-term evolution of upper stratospheric ozone at selected stations of the Network for the Detection of Stratospheric Change (NDSC)

    NARCIS (Netherlands)

    Steinbrecht, W; Claude, H; Schönenborn, F; McDermid, I S; Leblanc, T; Godin, S; Song, T; Swart, D P J; Meijer, Y J; Bodeker, G E; Connor, B J; Kämpfer, N; Hocke, K; Calisesi, Y; Schneider, N; Noë, J de la; Parrish, A D; Boyd, I S; Brühl, C; Steil, B; Giorgetta, M A; Manzini, E; Thomason, L W; Zawodny, J M; McCormick, M P; Russell, J M; Bhartia, P K; Stolarski, R S; Hollandsworth-Frith, S M

    2006-01-01

    The long-term evolution of upper stratospheric ozone has been recorded by lidars and microwave radiometers within the ground-based Network for the Detection of Stratospheric Change (NDSC), and by the space-borne Solar Backscatter Ultra-Violet instruments (SBUV), Stratospheric Aerosol and Gas

  2. An overview of regional and local characteristics of aerosols in South Africa using satellite, ground, and modeling data

    Directory of Open Access Journals (Sweden)

    S. P. Hersey

    2014-09-01

    Full Text Available We present a comprehensive overview of particulate air quality across the five major metropolitan areas of South Africa (Cape Town, Bloemfontein, Johannesburg and Tshwane (Gauteng Province, the Industrial Highveld Air Quality Priority Area (HVAPA, and Durban, based on a decadal (1 January 2000 to 31 December 2009 aerosol climatology from multiple satellite platforms and a detailed analysis of ground-based data from 19 sites throughout Gauteng. Data include Aerosol Optical Depth (AOD550, 555 from Aqua (550 nm, Terra (550 nm, and MISR (555 nm platforms, Ängström Exponent (α550/865, 470/660 from Aqua (550/865 nm and Terra (470/660 nm, Ultraviolet Aerosol Index (UVAI from TOMS, and model results from the Goddard Ozone Chemistry Aerosol Radiation and Transport (GOCART model. Results in Cape Town are distinct, owing to a typically clean, marine airmass origin and infrequent continental influence. At continentally-influenced sites, AOD550, AOD555, α550/865, α470/660 and UVAI reach maxima (0.12–0.20, 1.0–1.8, and 1.0–1.2, respectively during late winter and early spring (August–October, coinciding with a period of enhanced dust generation and the maximum frequency of close-proximity and subtropical fires identified by MODIS Fire Information for Resource Management System (FIRMS. The adjacent metropolitan and industrial Gauteng and HVAPA areas have been identified as a megacity based on NO2 concentrations, but AOD is a factor of 3–6 lower than other megacities worldwide. GOCART results suggest that the contributions of organics and black carbon to AOD are significantly enhanced during biomass burning season (ASO, but that sulfate is the most significant contributor to AOD (~70–80% through the rest of the year. Dust appears to be underestimated by GOCART emissions inventories at continentally-influenced metropolitan areas of South Africa. Ground monitoring sites were classified according to site type: (1 township and informal settlement

  3. In situ and space-based observations of the Kelud volcanic plume: The persistence of ash in the lower stratosphere

    Science.gov (United States)

    Vernier, Jean-Paul; Fairlie, T. Duncan; Deshler, Terry; Natarajan, Murali; Knepp, Travis; Foster, Katie; Wienhold, Frank G.; Bedka, Kristopher M.; Thomason, Larry; Trepte, Charles

    2016-09-01

    Volcanic eruptions are important causes of natural variability in the climate system at all time scales. Assessments of the climate impact of volcanic eruptions by climate models almost universally assume that sulfate aerosol is the only radiatively active volcanic material. We report satellite observations from the Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP) on board the Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observations (CALIPSO) satellite after the eruption of Mount Kelud (Indonesia) on 13 February 2014 of volcanic materials in the lower stratosphere. Using these observations along with in situ measurements with the Compact Optical Backscatter AerosoL Detector (COBALD) backscatter sondes and optical particle counters (OPCs) made during a balloon field campaign in northern Australia, we find that fine ash particles with a radius below 0.3 µm likely represented between 20 and 28% of the total volcanic cloud aerosol optical depth 3 months after the eruption. A separation of 1.5-2 km between the ash and sulfate plumes is observed in the CALIOP extinction profiles as well as in the aerosol number concentration measurements of the OPC after 3 months. The settling velocity of fine ash with a radius of 0.3 µm in the tropical lower stratosphere is reduced by 50% due to the upward motion of the Brewer-Dobson circulation resulting a doubling of its lifetime. Three months after the eruption, we find a mean tropical clear-sky radiative forcing at the top of the atmosphere from the Kelud plume near -0.08 W/m2 after including the presence of ash; a value 20% higher than if sulfate alone is considered. Thus, surface cooling following volcanic eruptions could be affected by the persistence of ash and should be considered in climate simulations.

  4. Stratospheric ozone

    Directory of Open Access Journals (Sweden)

    M. Gil

    2006-01-01

    Full Text Available Stratospheric ozone acquired a huge importance two decades ago because of the discovery of strong anomalies above the Antarctica due to gases of anthropogenic origin. From that date, stratosphere has become one of the research lines receiving more funding. A result, an important progress in the development of observational techniques, the understanding of the dynamics of the polar regions and, above all, in understanding of the chemical interactions among the species that influence the chemical-radiative balance of ozone. In this article a general revision is made of the distribution of the ozone in the stratosphere, the mechanisms that determine its equilibrium, the gases that contribute to its destruction, the present situation and the forecast of the health state of the layer.

  5. The relationship between cloud condensation nuclei (CCN concentration and light extinction of dried particles: indications of underlying aerosol processes and implications for satellite-based CCN estimates

    Directory of Open Access Journals (Sweden)

    Y. Shinozuka

    2015-01-01

    Full Text Available We examine the relationship between the number concentration of boundary-layer cloud condensation nuclei (CCN and light extinction to investigate underlying aerosol processes and satellite-based CCN estimates. Regression applied to a variety of airborne and ground-based measurements identifies the CCN (cm−3 at 0.4 ± 0.1% supersaturation with 100.3α +1.3 σ0.75 where σ (M m−1 is the 500 nm extinction coefficient by dried particles and α is the Angstrom exponent. The deviation of one kilometer horizontal average data from this approximation is typically within a factor of 2.0. ∂ log CCN/∂ log σ is less than unity because, among other explanations, aerosol growth processes generally make particles scatter more light without increasing their number. This, barring extensive data aggregation and special meteorology-aerosol connections, associates doubling of aerosol optical depth with less than doubling of CCN, contrary to common assumptions in satellite-based analysis of aerosol-cloud interactions.

  6. Validation of Two MODIS Aerosols Algorithms with SKYNET and Prospects for Future Climate Satellites Such as the GCOM-C/SGLI

    Directory of Open Access Journals (Sweden)

    Jules R. Dim

    2013-01-01

    Full Text Available Potential improvements of aerosols algorithms for future climate-oriented satellites such as the coming Global Change Observation Mission Climate/Second generation Global Imager (GCOM-C/SGLI are discussed based on a validation study of three years’ (2008–2010 daily aerosols properties, that is, the aerosol optical thickness (AOT and the Ångström exponent (AE retrieved from two MODIS algorithms. The ground-truth data used for this validation study are aerosols measurements from 3 SKYNET ground sites. The results obtained show a good agreement between the ground-truth data AOT and that of one of the satellites’ algorithms, then a systematic overestimation (around 0.2 by the other satellites’ algorithm. The examination of the AE shows a clear underestimation (by around 0.2–0.3 by both satellites’ algorithms. The uncertainties explaining these ground-satellites’ algorithms discrepancies are examined: the cloud contamination affects differently the aerosols properties (AOT and AE of both satellites’ algorithms due to the retrieval scale differences between these algorithms. The deviation of the real part of the refractive index values assumed by the satellites’ algorithms from that of the ground tends to decrease the accuracy of the AOT of both satellites’ algorithms. The asymmetry factor (AF of the ground tends to increase the AE ground-satellites discrepancies as well.

  7. Chasing the Black Smoke: Building Software for CALIPSO Satellite Data to Aid in Tracking and Identifying Sources of Aerosols and their Impact on the Earth's Climate

    Science.gov (United States)

    Mercer, G. A.

    2015-12-01

    The Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observation (CALIPSO) satellite is a NASA Earth observation that analyzes aerosol particles suspended in the Earth's atmosphere. Researchers use visualized CALIPSO data to track the global distribution, dispersion, and source of aerosols. There currently exists a tool for displaying CALIPSO data, but this tool does not support needed features for tracking aerosols such as selecting regions of data and sharing those selected regions, making tracking specific airborne objects difficult for researchers. Adding these necessary features to the current CALIPSO visualization tool is difficult, as the tool is written in Interactive Data Language (IDL), a proprietary and obscure language and writing additional features for the tool would require a specialized development team. This topic will focus on release of a new tool for visualization CALIPSO's atmospheric data, or the Visualization of CALIPSO (VOCAL) open source Python program. The talk will explain why VOCAL will serve as the successor to the current visualization tool for CALIPSO data, what new features VOCAL brings to the table for researchers, and how this new tool can further support the tracking and identification of aerosols in the Earth's atmosphere.

  8. Particulate sulfur in the upper troposphere and lowermost stratosphere – sources and climate forcing

    Directory of Open Access Journals (Sweden)

    B. G. Martinsson

    2017-09-01

    Full Text Available This study is based on fine-mode aerosol samples collected in the upper troposphere (UT and the lowermost stratosphere (LMS of the Northern Hemisphere extratropics during monthly intercontinental flights at 8.8–12 km altitude of the IAGOS-CARIBIC platform in the time period 1999–2014. The samples were analyzed for a large number of chemical elements using the accelerator-based methods PIXE (particle-induced X-ray emission and PESA (particle elastic scattering analysis. Here the particulate sulfur concentrations, obtained by PIXE analysis, are investigated. In addition, the