WorldWideScience

Sample records for high aerosol concentrations

  1. High Concentration Standard Aerosol Generator.

    Science.gov (United States)

    1985-07-31

    materials. In addition to material problems, many liquids are extremely flammable or explosive when aerosolized. This can be checked by putting a small...Hochriner. D. (1975) Stub 3A 440-445. St6ber, W. Flachsbart, H. and Hochramn, D. (1970) Staub 3^, 277. Yoshida. H. Fujii, K. Yomimoto, Y. Masuda. H. and

  2. Unexpectedly high ultrafine aerosol concentrations above East Antarctic sea-ice

    Directory of Open Access Journals (Sweden)

    R. S. Humphries

    2015-10-01

    Full Text Available The effect of aerosols on clouds and their radiative properties is one of the largest uncertainties in our understanding of radiative forcing. A recent study has concluded that better characterisation of pristine, natural aerosol processes leads to the largest reduction in these uncertainties. Antarctica, being far from anthropogenic activities, is an ideal location for the study of natural aerosol processes. Aerosol measurements in Antarctica are often limited to boundary layer air-masses at spatially sparse coastal and continental research stations, with only a handful of studies in the sea ice region. In this paper, the first observational study of sub-micron aerosols in the East Antarctic sea ice region is presented. Measurements were conducted aboard the ice-breaker Aurora Australis in spring 2012 and found that boundary layer condensation nuclei (CN3 concentrations exhibited a five-fold increase moving across the Polar Front, with mean Polar Cell concentrations of 1130 cm−3 – higher than any observed elsewhere in the Antarctic and Southern Ocean region. The absence of evidence for aerosol growth suggested that nucleation was unlikely to be local. Air parcel trajectories indicated significant influence from the free troposphere above the Antarctic continent, implicating this as the likely nucleation region for surface aerosol, a similar conclusion to previous Antarctic aerosol studies. The highest aerosol concentrations were found to correlate with low pressure systems, suggesting that the passage of cyclones provided an accelerated pathway, delivering air-masses quickly from the free-troposphere to the surface. After descent from the Antarctic free troposphere, trajectories suggest that sea ice boundary layer air-masses travelled equator-ward into the low albedo Southern Ocean region, transporting with them emissions and these aerosol nuclei where, after growth, may potentially impact on the region's radiative balance. The high aerosol

  3. Lidar detection of high concentrations of ozone and aerosol transported from northeastern Asia over Saga, Japan

    Science.gov (United States)

    Uchino, Osamu; Sakai, Tetsu; Izumi, Toshiharu; Nagai, Tomohiro; Morino, Isamu; Yamazaki, Akihiro; Deushi, Makoto; Yumimoto, Keiya; Maki, Takashi; Tanaka, Taichu Y.; Akaho, Taiga; Okumura, Hiroshi; Arai, Kohei; Nakatsuru, Takahiro; Matsunaga, Tsuneo; Yokota, Tatsuya

    2017-02-01

    To validate products of the Greenhouse gases Observing SATellite (GOSAT), we observed vertical profiles of aerosols, thin cirrus clouds, and tropospheric ozone with a mobile-lidar system that consisted of a two-wavelength (532 and 1064 nm) polarization lidar and a tropospheric ozone differential absorption lidar (DIAL). We used these lidars to make continuous measurements over Saga (33.24° N, 130.29° E) during 20-31 March 2015. High ozone and high aerosol concentrations were observed almost simultaneously in the altitude range 0.5-1.5 km from 03:00 to 20:00 Japan Standard Time (JST) on 22 March 2015. The maximum ozone volume mixing ratio was ˜ 110 ppbv. The maxima of the aerosol extinction coefficient and optical depth at 532 nm were 1.2 km-1 and 2.1, respectively. Backward trajectory analysis and the simulations by the Model of Aerosol Species IN the Global AtmospheRe (MASINGAR) mk-2 and the Meteorological Research Institute Chemistry-Climate Model, version 2 (MRI-CCM2), indicated that mineral dust particles from the Gobi Desert and an air mass with high ozone and aerosol (mainly sulfate) concentrations that originated from the North China Plain could have been transported over the measurement site within about 2 days. These high ozone and aerosol concentrations impacted surface air quality substantially in the afternoon of 22 March 2015. After some modifications of its physical and chemical parameters, MRI-CCM2 approximately reproduced the high ozone volume mixing ratio. MASINGAR mk-2 successfully predicted high aerosol concentrations, but the predicted peak aerosol optical thickness was about one-third of the observed value.

  4. Real-time measurement of aerosol particle concentration at high temperatures; Hiukkaspitoisuuden reaaliaikainen mittaaminen korkeassa laempoetilassa

    Energy Technology Data Exchange (ETDEWEB)

    Keskinen, J.; Hautanen, J.; Laitinen, A. [Tampere Univ. of Technology (Finland). Physics

    1997-10-01

    The aim of this project is to develop a new method for continuous aerosol particle concentration measurement at elevated temperatures (up to 800-1000 deg C). The measured property of the aerosol particles is the so called Fuchs surface area. This quantity is relevant for diffusion limited mass transfer to particles. The principle of the method is as follows. First, aerosol particles are charged electrically by diffusion charging process. The charging takes place at high temperature. After the charging, aerosol is diluted and cooled. Finally, aerosol particles are collected and the total charge carried by the aerosol particles is measured. Particle collection and charge measurement take place at low temperature. Benefits of this measurement method are: particles are charged in-situ, charge of the particles is not affected by the temperature and pressure changes after sampling, particle collection and charge measurement are carried out outside the process conditions, and the measured quantity is well defined. The results of this study can be used when the formation of the fly ash particles is studied. Another field of applications is the study and the development of gasification processes. Possibly, the method can also be used for the monitoring the operation of the high temperature particle collection devices. (orig.)

  5. High aerosol acidity despite declining atmospheric sulfate concentrations over the past 15 years

    Science.gov (United States)

    Weber, Rodney J.; Guo, Hongyu; Russell, Armistead G.; Nenes, Athanasios

    2016-04-01

    Particle acidity affects aerosol concentrations, chemical composition and toxicity. Sulfate is often the main acid component of aerosols, and largely determines the acidity of fine particles under 2.5 μm in diameter, PM2.5. Over the past 15 years, atmospheric sulfate concentrations in the southeastern United States have decreased by 70%, whereas ammonia concentrations have been steady. Similar trends are occurring in many regions globally. Aerosol ammonium nitrate concentrations were assumed to increase to compensate for decreasing sulfate, which would result from increasing neutrality. Here we use observed gas and aerosol composition, humidity, and temperature data collected at a rural southeastern US site in June and July 2013 (ref. ), and a thermodynamic model that predicts pH and the gas-particle equilibrium concentrations of inorganic species from the observations to show that PM2.5 at the site is acidic. pH buffering by partitioning of ammonia between the gas and particle phases produced a relatively constant particle pH of 0-2 throughout the 15 years of decreasing atmospheric sulfate concentrations, and little change in particle ammonium nitrate concentrations. We conclude that the reductions in aerosol acidity widely anticipated from sulfur reductions, and expected acidity-related health and climate benefits, are unlikely to occur until atmospheric sulfate concentrations reach near pre-anthropogenic levels.

  6. Out of Africa: High aerosol concentrations in the upper troposphere over Africa

    Directory of Open Access Journals (Sweden)

    J. Heintzenberg

    2003-05-01

    Full Text Available In the year 2000, six flights (three southbound and three northbound of the CARIBIC project were conducted between Germany and two destinations in the southern hemisphere (Windhoek, Namibia and Cape Town, South Africa. In the present report, results on particle number concentrations are discussed in three size ranges (>4 nm, >12 nm, and >18 nm particle diameter during the unique transequatorial Africa flights. The flights covered a total of about 80 h in May, July, and December. Thus, no claim can be made for long-term representativeness of the aerosol data. Nevertheless, they are the first upper systematic tropospheric transequatorial aerosol profiles over Africa. The average aerosol results show a broad maximum, roughly symmetrical to the equator, which compares well in latitudinal extent to a maximum of CO concentrations measured on the same flights. This export of continental surface aerosol to the upper troposphere will be dispersed on a global scale both with the easterly flow near the equator and with the westerlies in the adjacent subtropical regions. There was strong evidence of recent new particle formation before aerosol arrival at flight level, in particular during the time periods between 9:00 and 13:00 local time over Africa. Direct and indirect climate effects of the respective particulate matter remain to be investigated by future flights with the ongoing extension of the CARIBIC payload towards size-resolved measurements above 100 nm particle diameter. At the same time global chemical transport models and aerosol dynamics models need to be extended to be able to reproduce the CARIBIC findings over Africa.

  7. Systematic aerosol characterization by combining GOME-2 UV Aerosol Indices with trace gas concentrations

    Science.gov (United States)

    Penning de Vries, M.; Stammes, P.; Wagner, T.

    2012-04-01

    The task of determining aerosol type using passive remote sensing instruments is a daunting one. First, because the variety in aerosol (optical) properties is very large; and second, because the effect of aerosols on the detected top-of-atmosphere reflectance spectrum is smooth and mostly featureless. In addition, spectrometers like GOME-2 have a coarse spatial resolution, which makes aerosol characterization even more difficult due to interferences with clouds. On account of these problems, we do not attempt to derive aerosol properties from single measurements: instead, we combine time series of UV Aerosol Index and trace gas concentrations to derive the dominating aerosol type for each season. Aside from the Index values and trace gas concentrations themselves, the correlation between UV Aerosol Indices (which are indicative of aerosol absorption) with NO2, HCHO, and CHOCHO columns - or absence of it - provides clues to the (main) source of the aerosols in the investigated region and time range. For example: a high correlation of HCHO and Absorbing Aerosol Index points to aerosols from biomass burning, highly correlated CHOCHO, HCHO, and SCattering Index indicate biogenic secondary organic aerosols, and coinciding high NO2 concentrations with high SCattering Index values are associated with industrial and urban aerosols. We here present case studies for several regions to demonstrate the suitability of our approach. Then, we introduce a method to systematically derive the dominating aerosol type on a global scale on time scales varying from monthly to yearly.

  8. Highly time-resolved trace element concentrations in aerosols during the Megapoli Paris campaigns

    Science.gov (United States)

    Furger, Markus; Visser, Suzanne; Slowik, Jay G.; Crippa, Monica; Poulain, Laurent; Appel, Karen; Flechsig, Uwe; Prevot, Andre S. H.; Baltensperger, Urs

    2014-05-01

    Trace elements contribute typically only a few percent to the total mass of air pollutants, however, they can affect the environment in significant ways, especially those that are toxic. Furthermore, they are advantageous with respect to a refinement of source apportionment when measured with high time resolution and appropriate size segregation. This approach is especially advantageous in an urban environment with numerous time-variant emission sources distributed across a relatively narrow space, as is typically the setting of a megacity. Two 1-month long field campaigns took place in the framework of the Megapoli project in Paris, France, in the summer of 2009 and in the winter of 2010. Rotating drum impactors (RDI) were operated at two sites in each campaign, one urban, the other one suburban. The RDI segregated the aerosols into three size ranges (PM10-2.5, PM2.5-1 and PM1-0.1) and sampled with 2-hour time resolution. The samples were analyzed with synchrotron radiation induced X-ray fluorescence spectrometry (SR-XRF) at the synchrotron facilities of Paul Scherrer Institute (SLS) and Deutsches Elektronen-Synchrotron (HASYLAB), where a broad range of elements (Na, Mg, Al, Si, P, S, Cl, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Se, Sr, Zr, Cd, Sn, Sb, Ba, Pb) was analyzed for each size range. Time series of the analyzed elements for the different sites and campaigns were prepared to characterize the aerosol trace element composition and temporal behavior for the different weather situations and urban environments. They allow for the distinction of regional vs. local sources and transport, and provide a basis for source apportionment calculations. Local and regional contributions of traffic, including re-suspension, break wear and exhaust, wood burning, marine and other sources will be discussed. Indications of long-range transport from Polish coal emissions in the city center of Paris were also found.

  9. A case study of high sea salt aerosol (SSA) concentrations as a hazard to aviation

    OpenAIRE

    2015-01-01

    Abstract: On the night of 2nd January 2014 an aircraft on approach to Cork airport was required to abort a landing attempt due to sea salt aerosol (SSA) accretion on the windscreen. The salt reduced forward facing visibility to dangerously low levels. This was the first time such an incident was recorded by Irelands Air Accident Investigation Unit. This paper describes the meteorological conditions at the time of the aborted landing approach. Sea salt aerosol formation mechanisms are ela...

  10. Reconstruction of Aerosol Concentration and Composition from Glacier Ice Cores

    Science.gov (United States)

    Vogel, Alexander; Dällenbach, Kaspar; El-Haddad, Imad; Wendl, Isabel; Eichler, Anja; Schwikowski, Margit

    2017-04-01

    Reconstruction of the concentration and composition of natural aerosol in an undisturbed atmosphere enables the evaluation of the understanding of aerosol-climate effects, which is currently based on highly uncertain emission inventories of the biosphere under pre-industrial conditions. Understanding of the natural state of the pre-industrial atmosphere and evaluating the atmospheric perturbations by anthropogenic emissions, and their potential feedbacks, is essential for accurate model predictions of the future climate (Boucher et al., 2013). Here, we present a new approach for the chemical characterization of the organic fraction preserved in cold-glacier ice cores. From this analysis historic trends of atmospheric organic aerosols are reconstructed, allowing new insights on organic aerosol composition and mass in the pre-industrial atmosphere, which can help to improve climate models through evaluation of our current understanding of aerosol radiative effects. We present results from a proof-of-principal study, analyzing an 800 year ice core record from the Lomonosovfonna glacier ice core, drilled in 2009 in Svalbard, Norway, using a setup that has until then only been applied on offline measurements of aerosol filter extracts (Dällenbach et al., 2016): The melted ice was nebulized and dried, such that aerosols are formed from the soluble and insoluble organic and inorganic compounds that are preserved in the ice. To improve the sensitivity, the aerosol stream was then enriched by the application of an online aerosol concentrator, before the aerosol was analyzed by electron ionization within a high resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS). We were able to demonstrate that this setup is a quantitative method toward nitrate and sulfate when internal inorganic standards of NH415NO3 and (NH4)234SO4 are added to the sample. Comparison between AMS and IC measurements of nitrate and sulfate resulted in an excellent agreement. The analysis of

  11. MCS precipitation and downburst intensity response to increased aerosol concentrations

    Science.gov (United States)

    Clavner, M.; Cotton, W. R.; van den Heever, S. C.

    2015-12-01

    Mesoscale convective systems (MCSs) are important contributors to rainfall in the High Plains of the United States as well as producers of severe weather such as hail, tornados and straight-line wind events known as derechos. Past studies have shown that changes in aerosol concentrations serving as cloud condensation nuclei (CCN) alter the MCS hydrometeor characteristics which in turn modify precipitation yield, downdraft velocity, cold-pool strength, storm propagation and the potential for severe weather to occur. In this study, the sensitivity of MCS precipitation characteristics and convective downburst velocities associated with a derecho to changes in CCN concentrations were examined by simulating a case study using the Regional Atmospheric Modeling System (RAMS). The case study of the 8 May 2009 "Super-Derecho" MCS was chosen since it produced a swath of widespread wind damage in association with an embedded large-scale bow echo, over a broad region from the High Plains of western Kansas to the foothills of the Appalachians. The sensitivity of the storm to changes in CCN concentrations was examined by conducting a set of three simulations which differed in the initial aerosol concentration based on output from the 3D chemical transport model, GEOS-Chem. Results from this study indicate that while increasing CCN concentrations led to an increase in precipitation rates, the changes to the derecho strength were not linear. A moderate increase in aerosol concentration reduced the derecho strength, while the simulation with the highest aerosol concentrations increased the derecho intensity. These changes are attributed to the impact of enhanced CCN concentration on the production of convective downbursts. An analysis of aerosol loading impacts on these MCS features will be presented.

  12. VERTICAL DISTRIBUTION OF ATMOSPHERIC AEROSOL CONCENTRATION AT XIANGHE

    Institute of Scientific and Technical Information of China (English)

    Li Xu; Guangyu Shi; Jun Zhou; Yasunobu Iwasaka

    2004-01-01

    This paper summarizes atmospheric aerosol concentrations of 5 stratospheric balloon soundings during the period from 1984 to 1994. Aerosol-rich layers in the troposphere were detected and the causes were analyzed. The main results are as follows: (1) the vertical distribution of the atmospheric aerosol is affected by atmospheric dynamic processes, humidity, etc.; (2) the tropospheric column concentrations of aerosol were 72.2×105, 20.2×105, 20.7×105 and 34.4×105 cm-2 and occupying 81%, 61% and 60% of the 0-to-30 km aerosol column, on Aug. 23, 1984, Aug. 22, 1993,Sept. 12, 1993 and Sept. 15, 1994, respectively; (3) the effect of volcano eruption was still evident in the aerosol profiles,28 and 27 months after the El Chichon and Pinatubo eruption; (4) the aerosol concentration in the troposphere did not decrease at all heights as atmospheric aerosol model.

  13. Characterization of aerosol composition, concentrations, and sources at Baengnyeong Island, Korea using an aerosol mass spectrometer

    Science.gov (United States)

    Lee, Taehyoung; Choi, Jinsoo; Lee, Gangwoong; Ahn, Junyoung; Park, Jin Soo; Atwood, Samuel A.; Schurman, Misha; Choi, Yongjoo; Chung, Yoomi; Collett, Jeffrey L.

    2015-11-01

    To improve understanding of the sources and chemical properties of particulate pollutants on the western side of the Korean Peninsula, an Aerodyne High Resolution Time of Flight Aerosol Mass Spectrometer (HR-ToF-AMS) measured non-refractory fine (PM1) particles from May to November, 2011 at Baengnyeong Island, South Korea. Organic matter and sulfate were generally the most abundant species and exhibited maximum concentrations of 36 μg/m3 and 39 μg/m3, respectively. Nitrate concentrations peaked at 32 μg/m3 but were typically much lower than sulfate and organic matter concentrations. May, September, October, and November featured the highest monthly average concentrations, with lower concentrations typically observed from June through August. Potential source contribution function (PSCF) analysis and individual case studies revealed that transport from eastern China, an area with high SO2 emissions, was associated with high particulate sulfate concentrations at the measurement site. Observed sulfate aerosol sometimes was fully neutralized by ammonium but often was acidic; the average ammonium to sulfate molar ratio was 1.49. Measured species size distributions revealed a range of sulfate particle size distributions with modes between 100 and 600 nm. Organic aerosol source regions were widespread, including contributions from eastern China and South Korea. Positive matrix factorization (PMF) analysis indicated three "factors," or types of organic aerosol, comprising one primary, hydrocarbon-like organic aerosol (HOA) and two oxidized organic aerosol (OOA) components, including a more oxidized (MO-OOA) and a less oxidized (LO-OOA) oxidized organic aerosol. On average, HOA and OOA contributed 21% and 79% of the organic mass (OM), respectively, with the MO-OOA fraction nearly three times as abundant as the LO-OOA fraction. Biomass burning contributions to observed OM were low during the late spring/early summer agricultural burning season in eastern China, since

  14. Highly Resolved Paleoclimatic Aerosol Records

    DEFF Research Database (Denmark)

    Kettner, Ernesto

    In ice cores a plethora of proxies for paleoclimatic conditions is archived. Air trapped in the ice during firnification allows for direct measurements of the concentrations and isotope ratios of paleoatmospheric gases while, the isotopic composition of the ice matrix itself is related...... to paleotemperatures. Impurities in the matrix are comprised of particulate and soluble aerosols, each carrying information on its source’s activitiy and|or proximity. Opposed to gases and water isotopes, the seasonality of many aerosols is not smoothed out in the firn column so that large concentration gradients...... with frequently changing signs are preserved. Therefore, these aerosol records can be used for dating by annual layer counting. However, with increasing depth the annual layer thicknesses decreases due to pressure and ice flow and accurate dating is possible only as long as the rapid variations can be resolved...

  15. Theoretical basis for convective invigoration due to increased aerosol concentration

    Directory of Open Access Journals (Sweden)

    Z. J. Lebo

    2011-06-01

    Full Text Available The potential effects of increased aerosol loading on the development of deep convective clouds and resulting precipitation amounts are studied by employing the Weather Research and Forecasting (WRF model as a detailed high-resolution cloud resolving model (CRM with both detailed bulk and bin microphysics schemes. Both models include a physically-based activation scheme that incorporates a size-resolved aerosol population. We demonstrate that the aerosol-induced effect is controlled by the balance between latent heating and the increase in condensed water aloft, each having opposing effects on buoyancy. It is also shown that under polluted conditions, increases in the CCN number concentration reduce the cumulative precipitation due to the competition between the sedimentation and evaporation/sublimation timescales. The effect of an increase in the IN number concentration on the dynamics of deep convective clouds is small and the resulting decrease in domain-averaged cumulative precipitation is shown not to be statistically significant, but may act to suppress precipitation. It is also shown that even in the presence of a decrease in the domain-averaged cumulative precipitation, an increase in the precipitation variance, or in other words, andincrease in rainfall intensity, may be expected in more polluted environments, especially in moist environments.

    A significant difference exists between the predictions based on the bin and bulk microphysics schemes of precipitation and the influence of aerosol perturbations on updraft velocity within the convective core. The bulk microphysics scheme shows little change in the latent heating rates due to an increase in the CCN number concentration, while the bin microphysics scheme demonstrates significant increases in the latent heating aloft with increasing CCN number concentration. This suggests that even a detailed two-bulk microphysics scheme, coupled to a detailed activation scheme, may not be

  16. Influence of the Surf Zone on the Marine Aerosol Concentration in a Coastal Area

    Science.gov (United States)

    Tedeschi, Gilles; van Eijk, Alexander M. J.; Piazzola, Jacques; Kusmierczyk-Michulec, Jolanta T.

    2017-01-01

    Sea-salt aerosol concentrations in the coastal zone are assessed with the numerical aerosol-transport model MACMod that applies separate aerosol source functions for open ocean and the surf zone near the sea-land transition. Numerical simulations of the aerosol concentration as a function of offshore distance from the surf zone compare favourably with experimental data obtained during a surf-zone aerosol experiment in Duck, North Carolina in autumn 2007. Based on numerical simulations, the effect of variations in aerosol production (source strength) and transport conditions (wind speed, air-sea temperature difference), we show that the surf-zone aerosols are replaced by aerosols generated over the open ocean as the airmass advects out to sea. The contribution from the surf-generated aerosol is significant during high wind speeds and high wave events, and is significant up to 30 km away from the production zone. At low wind speeds, the oceanic component dominates, except within 1-5 km of the surf zone. Similar results are obtained for onshore flow, where no further sea-salt aerosol production occurs as the airmass advects out over land. The oceanic aerosols that are well-mixed throughout the boundary layer are then more efficiently transported inland than are the surf-generated aerosols, which are confined to the first few tens of metres above the surface, and are therefore also more susceptible to the type of surface (trees or grass) that determines the deposition velocity.

  17. Contribution of new particle formation to the total aerosol concentration at the high-altitude site Jungfraujoch (3580 m asl, Switzerland)

    Science.gov (United States)

    Tröstl, Jasmin; Herrmann, Erik; Frege, Carla; Bianchi, Federico; Molteni, Ugo; Bukowiecki, Nicolas; Hoyle, Christopher R.; Steinbacher, Martin; Weingartner, Ernest; Dommen, Josef; Gysel, Martin; Baltensperger, Urs

    2016-10-01

    Previous modeling studies hypothesized that a large fraction of cloud condensation nuclei (CCN) is attributed to new particle formation (NPF) in the free troposphere. Despite the potential importance of this process, only few long-term observations have been performed to date. Here we present the results of a 12 month campaign of NPF observations at the high-altitude site Jungfraujoch (JFJ, 3580 m above sea level (asl)). Our results show that NPF significantly adds to the total aerosol concentration at the JFJ and only occurs via previous precursor entrainment from the planetary boundary layer (PBL). Freshly nucleated particles do not directly grow to CCN size (90 nm) within observable time scales (maximum 48 h). The contribution of NPF to the CCN concentration is low within this time frame compared to other sources, such as PBL entrainment of larger particles. A multistep growth mechanism is proposed which allows previously formed Aitken mode particles to add to the CCN concentration. A parametrization is derived to explain formation rates at the JFJ, showing that precursor concentration, PBL influence, and global radiation are the key factors controlling new particle formation at the site.

  18. Theoretical basis for convective invigoration due to increased aerosol concentration

    Directory of Open Access Journals (Sweden)

    Z. J. Lebo

    2011-01-01

    Full Text Available The potential effects of increased aerosol loading on the development of deep convective clouds and resulting precipitation amounts are studied by employing the Weather Research and Forecasting (WRF model as a detailed high-resolution cloud resolving model (CRM with both detailed bulk and bin microphysics schemes. The bulk microphysics scheme incorporates a physically based parameterization of cloud droplet activation as well as homogeneous and heterogeneous freezing in order to explicitly resolve the possible aerosol-induced effects on the cloud microphysics. These parameterizations allow one to segregate the effects of an increase in the aerosol number concentration into enhanced cloud condensation nuclei (CCN and/or ice nuclei (IN concentrations using bulk microphysics. The bin microphysics scheme, with its explicit calculations of cloud particle collisions, is shown to better predict cumulative precipitation. Increases in the CCN number concentration may not have a monotonic influence on the cumulative precipitation resulting from deep convective clouds. We demonstrate that the aerosol-induced effect is controlled by the balance between latent heating and the increase in condensed water aloft, each having opposing effects on buoyancy. It is also shown that under polluted conditions and in relatively dry environments, increases in the CCN number concentration reduce the cumulative precipitation due to the competition between the sedimentation and evaporation/sublimation timescales. The effect of an increase in the IN number concentration on the dynamics of deep convective clouds is small, but may act to suppress precipitation.

    A comparison of the predictions using the bin and bulk microphysics schemes demonstrate a significant difference between the predicted precipitation and the influence of aerosol perturbations on updraft velocity within the convective core. The bulk microphysics scheme is shown to be unable to capture the

  19. The relationship between aerosol and cloud drop number concentrations in a global aerosol microphysics model

    Directory of Open Access Journals (Sweden)

    K. J. Pringle

    2009-01-01

    Full Text Available Empirical relationships that link cloud droplet number (CDN to aerosol number or mass are commonly used to calculate global fields of CDN for climate forcing assessments. In this work we use a sectional global model of sulfate and sea-salt aerosol coupled to a mechanistic aerosol activation scheme to explore the limitations of this approach. We find that a given aerosol number concentration produces a wide range of CDN concentrations due to variations in the shape of the aerosol size distribution. On a global scale, the dependence of CDN on the size distribution results in regional biases in predicted CDN (for a given aerosol number. Empirical relationships between aerosol number and CDN are often derived from regional data but applied to the entire globe. In an analogous process, we derive regional "correlation-relations" between aerosol number and CDN and apply these regional relations to calculations of CDN on the global scale. The global mean percentage error in CDN caused by using regionally derived CDN-aerosol relations is 20 to 26%, which is about half the global mean percentage change in CDN caused by doubling the updraft velocity. However, the error is as much as 25–75% in the Southern Ocean, the Arctic and regions of persistent stratocumulus when an aerosol-CDN correlation relation from the North Atlantic is used. These regions produce much higher CDN concentrations (for a given aerosol number than predicted by the globally uniform empirical relations. CDN-aerosol number relations from different regions also show very different sensitivity to changing aerosol. The magnitude of the rate of change of CDN with particle number, a measure of the aerosol efficacy, varies by a factor 4. CDN in cloud processed regions of persistent stratocumulus is particularly sensitive to changing aerosol number. It is therefore likely that the indirect effect will be underestimated in these important regions.

  20. The relationship between aerosol and cloud drop number concentrations in a global aerosol microphysics model

    Directory of Open Access Journals (Sweden)

    K. J. Pringle

    2009-06-01

    Full Text Available Empirical relationships that link cloud droplet number (CDN to aerosol number or mass are commonly used to calculate global fields of CDN for climate forcing assessments. In this work we use a sectional global model of sulfate and sea-salt aerosol coupled to a mechanistic aerosol activation scheme to explore the limitations of this approach. We find that a given aerosol number concentration produces a wide range of CDN concentrations due to variations in the shape of the aerosol size distribution. On a global scale, the dependence of CDN on the size distribution results in regional biases in predicted CDN (for a given aerosol number. Empirical relationships between aerosol number and CDN are often derived from regional data but applied to the entire globe. In an analogous process, we derive regional "correlation-relations" between aerosol number and CDN and apply these regional relations to calculations of CDN on the global scale. The global mean percentage error in CDN caused by using regionally derived CDN-aerosol relations is 20 to 26%, which is about half the global mean percentage change in CDN caused by doubling the updraft velocity. However, the error is as much as 25–75% in the Southern Ocean, the Arctic and regions of persistent stratocumulus when an aerosol-CDN correlation relation from the North Atlantic is used. These regions produce much higher CDN concentrations (for a given aerosol number than predicted by the globally uniform empirical relations. CDN-aerosol number relations from different regions also show very different sensitivity to changing aerosol. The magnitude of the rate of change of CDN with particle number, a measure of the aerosol efficacy, varies by a factor 4. CDN in cloud processed regions of persistent stratocumulus is particularly sensitive to changing aerosol number. It is therefore likely that the indirect effect will be underestimated in these important regions.

  1. Impacts of Wet Scavenging Parameterizations on Global Simulations of Aerosol Concentrations and Lifetimes (Invited)

    Science.gov (United States)

    Croft, B.; Martin, R.; Lohmann, U.; Pierce, J. R.

    2013-12-01

    Wet scavenging processes strongly control aerosol three-dimensional distributions. In this study, we quantify the uncertainty in global simulations of aerosol vertical profiles and lifetimes, which may be attributed to uncertainties in both convective and stratiform wet scavenging parameterizations. For convective clouds, we show that different assumptions about the wet removal of aerosols entrained above convective cloud bases can yield differences of about one order of magnitude in middle and upper tropospheric aerosol concentrations. For stratiform clouds, we demonstrate the impact of size-dependent aerosol wet scavenging as compared to the use of fixed prescribed scavenging coefficients. We quantify the difference in simulated aerosol concentrations, particularly at high latitudes, yielded by different assumptions about scavenging in mixed phase and ice clouds. We also examine the sensitivity of simulated global mean aerosol lifetimes to parameterizations for wet scavenging. Global simulations of the scavenging of aerosol-bound radionuclides following the Fukushima Dai-Ichi nuclear power plant accident are also presented. The simulated radionuclide lifetimes are compared to measurements. We present an interpretation of these constraints on global mean aerosol lifetimes. The sensitivity of simulated aerosol-bound radionuclide lifetimes to altitude and location of the radionuclide injection is also examined with consideration to the interplay of aerosol transport, mixing, and removal processes.

  2. Highly Resolved Paleoclimatic Aerosol Records

    DEFF Research Database (Denmark)

    Kettner, Ernesto

    experimentally. Over the last decades Continuous Flow Analysis (CFA) has become a well-established technique for aerosol quantification. In CFA, a piece of core is melted continuously and the melt water is analysed for an array of chemical impurities. When designing a CFA system, a trilemma between high sample...... with frequently changing signs are preserved. Therefore, these aerosol records can be used for dating by annual layer counting. However, with increasing depth the annual layer thicknesses decreases due to pressure and ice flow and accurate dating is possible only as long as the rapid variations can be resolved...... impossible to circumvent by employing a third detection technique - laser scattering. Reliable information on size changes, even relative ones, cannot be obtained using optical methods. It is therefore proposed to focus further efforts on electrical measurements, making use of the advancements made over...

  3. Warming-induced increase in aerosol number concentration likely to moderate climate change

    Science.gov (United States)

    Paasonen, Pauli; Asmi, Ari; Petäjä, Tuukka; Kajos, Maija K.; Äijälä, Mikko; Junninen, Heikki; Holst, Thomas; Abbatt, Jonathan P. D.; Arneth, Almut; Birmili, Wolfram; van der Gon, Hugo Denier; Hamed, Amar; Hoffer, András; Laakso, Lauri; Laaksonen, Ari; Richard Leaitch, W.; Plass-Dülmer, Christian; Pryor, Sara C.; Räisänen, Petri; Swietlicki, Erik; Wiedensohler, Alfred; Worsnop, Douglas R.; Kerminen, Veli-Matti; Kulmala, Markku

    2013-06-01

    Atmospheric aerosol particles influence the climate system directly by scattering and absorbing solar radiation, and indirectly by acting as cloud condensation nuclei. Apart from black carbon aerosol, aerosols cause a negative radiative forcing at the top of the atmosphere and substantially mitigate the warming caused by greenhouse gases. In the future, tightening of controls on anthropogenic aerosol and precursor vapour emissions to achieve higher air quality may weaken this beneficial effect. Natural aerosols, too, might affect future warming. Here we analyse long-term observations of concentrations and compositions of aerosol particles and their biogenic precursor vapours in continental mid- and high-latitude environments. We use measurements of particle number size distribution together with boundary layer heights derived from reanalysis data to show that the boundary layer burden of cloud condensation nuclei increases exponentially with temperature. Our results confirm a negative feedback mechanism between the continental biosphere, aerosols and climate: aerosol cooling effects are strengthened by rising biogenic organic vapour emissions in response to warming, which in turn enhance condensation on particles and their growth to the size of cloud condensation nuclei. This natural growth mechanism produces roughly 50% of particles at the size of cloud condensation nuclei across Europe. We conclude that biosphere-atmosphere interactions are crucial for aerosol climate effects and can significantly influence the effects of anthropogenic aerosol emission controls, both on climate and air quality.

  4. Effect of aerosol concentration and absorbing aerosol on the radiation fog life cycle

    Science.gov (United States)

    Maalick, Z.; Kühn, T.; Korhonen, H.; Kokkola, H.; Laaksonen, A.; Romakkaniemi, S.

    2016-05-01

    Analogous to cloud formation, the formation and life cycle of fogs is largely influenced by aerosol particles. The objective of this work is to analyze how changes in aerosol properties affect the fog life cycle, with special emphasis on how droplet concentrations change with cloud condensation nuclei (CCN) concentrations and on the effect that absorbing black carbon (BC) particles have on fog dissipation. For our simulation case study, we chose a typical fall time radiation fog at mid-latitudes (45° north) in fairly highly polluted conditions. Our results show that CCN concentrations have a strong influence on the fog lifetime. This is because the immediate effect of CCN on cloud droplet number concentrations (CDNC) is enhanced through two positive feedback loops: (1) Higher CDNC leads to more radiative cooling at the fog top, which leads to even stronger activation and (2) if CDNC is higher, the average droplet size is smaller, which slows down droplet removal through sedimentation. The effect that radiation fogs have on solar surface irradiation is large - the daily mean can change by 50% if CCN concentrations are doubled or halved (considering a reference CCN mixing ratio of 800 #/mg). With the same changes in CCN, the total fog lifetime increases 160 min or decreases 65 min, respectively. Although BC has a noticeable effect on fog height and dissipation time, its relative effect compared to CCN is small, even if BC concentrations are high. The fog formation is very sensitive to initial meteorological conditions which may be altered considerably if fog was present the previous day. This effect was neglected here, and future simulations, which span several days, may thus be a valuable extension of this study.

  5. Aerosol concentration and particle size distributions in underground excavations of a hard coal mine.

    Science.gov (United States)

    Skubacz, Krystian; Wojtecki, Łukasz; Urban, Paweł

    2017-09-01

    Deposition of aerosols in the respiratory system depends inter alia on their size and the respiratory tract deposition is appreciable for nanometer-sized particles. This article presents the results of measurements of size distributions of aerosols in the range of several nanometers up to about 20 μm in the underground mine excavations of an active hard coal mine. The study included practically all particles of a respirable fraction. The results showed that a high concentration of fine and ultrafine aerosols occurs in key underground workplaces especially during mining machine operations, although their contribution to total mass concentration is usually negligible.

  6. ANALYSIS OF PARTICULATE MASS CONCENTRATION, AEROSOL NUMBER CONCENTRATION AND VISIBILITY IN BEIJING

    Institute of Scientific and Technical Information of China (English)

    Fengqi Yan; Huanling Hu; Tong Yu

    2004-01-01

    Particulate mass concentration (PM10, PM2.5), aerosol number concentration (NOPC), aerosol size distribution and atmospheric visibility were simultaneously measured in Beijing in the summer and winter of 2001. From the profuse data collected, the following conclusions can be drown: (1) there are two peaks for the average diurnal variations of PM10 and NOPC in the summer, an obvious valley can be seen between 12:30 and 15:00 for their average diurnal variation in the winter; (2) there is one single peak for the average diurnal variation of atmospheric visibility in the summer,while there are two peaks in the winter; (3) PM10 and NOPC are usually smaller in the summer than those in the winter; (4)the average visibility is much lower during 00:00~09:00 in the summer than that in the winter, because of the very high relative humidity and higher concentration of the large particles (r>1.25 μm) in the summer during the period; (5) aerosol size distributions usually depend closely on season and relative humidity at the same place.

  7. A New Hybrid Spatio-temporal Model for Estimating Daily Multi-year PM2.5 Concentrations Across Northeastern USA Using High Resolution Aerosol Optical Depth Data

    Science.gov (United States)

    Kloog, Itai; Chudnovsky, Alexandra A.; Just, Allan C.; Nordio, Francesco; Koutrakis, Petros; Coull, Brent A.; Lyapustin, Alexei; Wang, Yujie; Schwartz, Joel

    2014-01-01

    The use of satellite-based aerosol optical depth (AOD) to estimate fine particulate matter PM(sub 2.5) for epidemiology studies has increased substantially over the past few years. These recent studies often report moderate predictive power, which can generate downward bias in effect estimates. In addition, AOD measurements have only moderate spatial resolution, and have substantial missing data. We make use of recent advances in MODIS satellite data processing algorithms (Multi-Angle Implementation of Atmospheric Correction (MAIAC), which allow us to use 1 km (versus currently available 10 km) resolution AOD data.We developed and cross validated models to predict daily PM(sub 2.5) at a 1X 1 km resolution across the northeastern USA (New England, New York and New Jersey) for the years 2003-2011, allowing us to better differentiate daily and long term exposure between urban, suburban, and rural areas. Additionally, we developed an approach that allows us to generate daily high-resolution 200 m localized predictions representing deviations from the area 1 X 1 km grid predictions. We used mixed models regressing PM(sub 2.5) measurements against day-specific random intercepts, and fixed and random AOD and temperature slopes. We then use generalized additive mixed models with spatial smoothing to generate grid cell predictions when AOD was missing. Finally, to get 200 m localized predictions, we regressed the residuals from the final model for each monitor against the local spatial and temporal variables at each monitoring site. Our model performance was excellent (mean out-of-sample R(sup 2) = 0.88). The spatial and temporal components of the out-of-sample results also presented very good fits to the withheld data (R(sup 2) = 0.87, R(sup)2 = 0.87). In addition, our results revealed very little bias in the predicted concentrations (Slope of predictions versus withheld observations = 0.99). Our daily model results show high predictive accuracy at high spatial resolutions

  8. Intercomparison of number concentration measurements by various aerosol particle counters

    Science.gov (United States)

    Ankilov, A.; Baklanov, A.; Colhoun, M.; Enderle, K.-H.; Gras, J.; Julanov, Yu.; Kaller, D.; Lindner, A.; Lushnikov, A. A.; Mavliev, R.; McGovern, F.; Mirme, A.; O'Connor, T. C.; Podzimek, J.; Preining, O.; Reischl, G. P.; Rudolf, R.; Sem, G. J.; Szymanski, W. W.; Tamm, E.; Vrtala, A. E.; Wagner, P. E.; Winklmayr, W.; Zagaynov, V.

    Total aerosol particle number concentrations, as measured by means of 16 different measurement systems, have been quantitatively compared during an international workshop at the Institute for Experimental Physics of the University of Vienna, Austria, which was coordinated within the Committee on Nucleation and Atmospheric Aerosols (ICCP-IUGG). The range of measuring instruments includes Pollak counters (PCO) in use already for several decades, presently available commercial particle counters, as well as laboratory prototypes. The operation of the instruments considered was based on different measurement principles: (1) adiabatic expansion condensation particle counter, (2) flow diffusion condensation particle counter, (3) turbulent mixing condensation particle counter, (4) laser optical particle counter, and (5) electrostatic particle measurement system. Well-defined test aerosols with various chemical compositions were considered: DEHS, sodium chloride, silver, hydrocarbons, and tungsten oxide. The test aerosols were nearly monodispersed with mean particle diameters between 4 and 520 nm, the particle number concentrations were varied over a range from about 4×10 1 to 7×10 6 cm -3. A few measurements were performed with two-component aerosol mixtures. For simultaneous concentration measurements, the various instruments considered were operated under steady state conditions in a linear flow system. A series of at least 10 single concentration measurements was performed by each individual instrument at each set of test aerosol parameters. The average of the concentration data measured by the various instruments was defined as a common reference. The number concentrations obtained from the various instruments typically agreed within a factor of about two over the entire concentration range considered. The agreement of the measured concentrations is notable considering the various different measurement principles applied in this study, and particularly in view of the

  9. Distributions and climate effects of atmospheric aerosols from the preindustrial era to 2100 along Representative Concentration Pathways (RCPs simulated using a global aerosol model SPRINTARS

    Directory of Open Access Journals (Sweden)

    T. Takemura

    2012-08-01

    Full Text Available Global distributions and associated climate effects of atmospheric aerosols were simulated using a global aerosol climate model, SPRINTARS, from 1850 to the present day and projected forward to 2100. Aerosol emission inventories used by the Coupled Model Intercomparison Project Phase 5 (CMIP5 were applied to this study. Scenarios based on the Representative Concentration Pathways (RCPs were used for the future projection. Aerosol loading in the atmosphere has already peaked and is now reducing in Europe and North America. However, in Asia where rapid economic growth is ongoing, aerosol loading is estimated to reach a maximum in the first half of this century. Atmospheric aerosols originating from the burning of biomass have maintained high loadings throughout the 21st century in Africa, according to the RCPs. Evolution of the adjusted forcing by direct and indirect aerosol effects over time generally correspond to the aerosol loading. The probable future pathways of global mean forcing differ based on the aerosol direct effect for different RCPs. Because aerosol forcing will be close to the preindustrial level by the end of the 21st century for all RCPs despite the continuous increases in greenhouse gases, global warming will be accelerated with reduced aerosol negative forcing.

  10. Distributions and climate effects of atmospheric aerosols from the preindustrial era to 2100 along Representative Concentration Pathways (RCPs simulated using the global aerosol model SPRINTARS

    Directory of Open Access Journals (Sweden)

    T. Takemura

    2012-12-01

    Full Text Available Global distributions and associated climate effects of atmospheric aerosols were simulated using a global aerosol climate model, SPRINTARS, from 1850 to the present day and projected forward to 2100. Aerosol emission inventories used by the Coupled Model Intercomparison Project Phase 5 (CMIP5 were applied to this study. Scenarios based on the Representative Concentration Pathways (RCPs were used for the future projection. Aerosol loading in the atmosphere has already peaked and is now reducing in Europe and North America. However, in Asia where rapid economic growth is ongoing, aerosol loading is estimated to reach a maximum in the first half of this century. Atmospheric aerosols originating from the burning of biomass have maintained high loadings throughout the 21st century in Africa, according to the RCPs. Evolution of the adjusted forcing by direct and indirect aerosol effects over time generally correspond to the aerosol loading. The probable future pathways of global mean forcing differ based on the aerosol direct effect for different RCPs. Because aerosol forcing will be close to the preindustrial level by the end of the 21st century for all RCPs despite the continuous increases in greenhouse gases, global warming will be accelerated with reduced aerosol negative forcing.

  11. Development of a continuous aerosol mass concentration measurement device.

    Science.gov (United States)

    Bémer, D; Thomas, D; Contal, P; Subra, I

    2003-08-01

    A dynamic aerosol mass concentration measurement device has been developed for personal sampling. Its principle consists in sampling the aerosol on a filter and monitoring the change of pressure drop over time (Delta P). Ensuring that the linearity of the Delta P = f(mass of particles per unit area of filter) relationship has been well established, the change of concentration can be deduced. The response of the system was validated in the laboratory with a 3.5 microm alumina aerosol (mass median diameter) generated inside a 1-m(3) ventilated enclosure. As the theory predicted that the mass sensitivity of the system would vary inversely with the square of the particle diameter, only sufficiently fine aerosols were able to be measured. The system was tested in the field in a mechanical workshop in the vicinity of an arc-welding station. The aerosol produced by welding is indeed particularly well-adapted due to the sub-micronic size of the particles. The device developed, despite this limitation, has numerous advantages over other techniques: robustness, compactness, reliability of calibration, and ease of use.

  12. Evaluation of aerosol number concentrations in NorESM with improved nucleation parameterisation

    Directory of Open Access Journals (Sweden)

    R. Makkonen

    2013-10-01

    Full Text Available The Norwegian Earth System Model (NorESM is evaluated against atmospheric observations of aerosol number concentrations. The model is extended to include an explicit mechanism for new particle formation, and the secondary organic aerosol (SOA formation from biogenic precursors is revised. Several model experiments are conducted to study the sensitivity of simulated number concentrations to nucleation, SOA formation, black carbon size distribution and model meteorology. Comparison against 60 measurement sites reveals that the model with improved nucleation and SOA scheme performs well in terms of correlation coefficient R2=0.41 calculated against monthly mean observed aerosol number concentrations with a number concentration bias of −6%. NorESM generally overestimates the amplitude of the seasonal cycle, possibly due to too high sensitivity to biogenic precursors. Simulated vertical profiles are also evaluated against 12 flight campaigns.

  13. Validation of LIRIC aerosol concentration retrievals using airborne measurements during a biomass burning episode over Athens

    Science.gov (United States)

    Kokkalis, Panagiotis; Amiridis, Vassilis; Allan, James D.; Papayannis, Alexandros; Solomos, Stavros; Binietoglou, Ioannis; Bougiatioti, Aikaterini; Tsekeri, Alexandra; Nenes, Athanasios; Rosenberg, Philip D.; Marenco, Franco; Marinou, Eleni; Vasilescu, Jeni; Nicolae, Doina; Coe, Hugh; Bacak, Asan; Chaikovsky, Anatoli

    2017-01-01

    In this paper we validate the Lidar-Radiometer Inversion Code (LIRIC) retrievals of the aerosol concentration in the fine mode, using the airborne aerosol chemical composition dataset obtained over the Greater Athens Area (GAA) in Greece, during the ACEMED campaign. The study focuses on the 2nd of September 2011, when a long-range transported smoke layer was observed in the free troposphere over Greece, in the height range from 2 to 3 km. CIMEL sun-photometric measurements revealed high AOD ( 0.4 at 532 nm) and Ångström exponent values ( 1.7 at 440/870 nm), in agreement with coincident ground-based lidar observations. Airborne chemical composition measurements performed over the GAA, revealed increased CO volume concentration ( 110 ppbv), with 57% sulphate dominance in the PM1 fraction. For this case, we compare LIRIC retrievals of the aerosol concentration in the fine mode with the airborne Aerosol Mass Spectrometer (AMS) and Passive Cavity Aerosol Spectrometer Probe (PCASP) measurements. Our analysis shows that the remote sensing retrievals are in a good agreement with the measured airborne in-situ data from 2 to 4 km. The discrepancies observed between LIRIC and airborne measurements at the lower troposphere (below 2 km), could be explained by the spatial and temporal variability of the aerosol load within the area where the airborne data were averaged along with the different time windows of the retrievals.

  14. Size-resolved morphological properties of the high Arctic summer aerosol during ASCOS-2008

    OpenAIRE

    Hamacher-Barth, Evelyne; Leck, Caroline; Jansson, Kjell

    2016-01-01

    The representation of aerosol properties and processes in climate models is fraught with large uncertainties. Especially at high northern latitudes a strong underprediction of aerosol concentrations and nucleation events is observed and can only be constrained by in situ observations based on the analysis of individual aerosol particles. To further reduce the uncertainties surrounding aerosol properties and their potential role as cloud condensation nuclei this study provide...

  15. Aerosol classification by airborne high spectral resolution lidar observations

    Directory of Open Access Journals (Sweden)

    S. Groß

    2012-10-01

    Full Text Available During four aircraft field experiments with the DLR research aircraft Falcon in 1998 (LACE, 2006 (SAMUM-1 and 2008 (SAMUM-2 and EUCAARI, airborne High Spectral Resolution Lidar (HSRL and in situ measurements of aerosol microphysical and optical properties were performed. Altogether, the properties of six different aerosol types and aerosol mixtures – Saharan mineral dust, Saharan dust mixtures, Canadian biomass burning aerosol, African biomass burning aerosol, anthropogenic pollution aerosol, and marine aerosol have been studied. On the basis of this extensive HSRL data set, we present an aerosol classification scheme which is also capable to identify mixtures of different aerosol types. We calculated mixing lines that allowed us to determine the contributing aerosol types. The aerosol classification scheme was validated with in-situ measurements and backward trajectory analyses. Our results demonstrate that the developed aerosol mask is capable to identify complex stratifications with different aerosol types throughout the atmosphere.

  16. Simultaneous retrieval of aerosol optical thickness and chlorophyll concentration from multiwavelength measurement over East China Sea

    Science.gov (United States)

    Shi, Chong; Nakajima, Teruyuki; Hashimoto, Makiko

    2016-12-01

    A flexible inversion algorithm is proposed for simultaneously retrieving aerosol optical thickness (AOT) and surface chlorophyll a (Chl) concentration from multiwavelength observation over the ocean. In this algorithm, forward radiation calculation is performed by an accurate coupled atmosphere-ocean model with a comprehensive bio-optical ocean module. Then, a full-physical nonlinear optimization approximation approach is used to retrieve AOT and Chl. For AOT retrieval, a global three-dimensional spectral radiation-transport aerosol model is used as the a priori constraint to increase the retrieval accuracy of aerosol. To investigate the algorithm's availability, the retrieval experiment is conducted using simulated radiance data to demonstrate that the relative errors in simultaneously determining AOT and Chl can be mostly controlled to within 10% using multiwavelength and angle covering in and out of sunglint. Furthermore, the inversion results are assessed using the actual satellite observation data obtained from Cloud and Aerosol Imager (CAI)/Greenhouse gas Observation SATellite GOSAT and MODerate resolution Imaging Spectroradiometer (MODIS)/Aqua instruments through comparison to Aerosol Robotic Network (AERONET) aerosol and ocean color (OC) products over East China Sea. Both the retrieved AOT and Chl compare favorably to the reported AERONET values, particularly when using the CASE 2 ocean module in turbid water, even when the retrieval is performed in the presence of high aerosol loading and sunglint. Finally, the CAI and MODIS images are used to jointly retrieve the spatial distribution of AOT and Chl in comparison to the MODIS AOT and OC products.

  17. Aerosol effects on ozone concentrations in Beijing: A model sensitivity study

    Institute of Scientific and Technical Information of China (English)

    Jun Xu; Yuanhang Zhang; Shaoqing Zheng; Youjiang He

    2012-01-01

    Most previous O3 simulations were based only on gaseous phase photochemistry.However,some aerosol-related processes,namely,heterogeneous reactions occurring on the aerosol surface and photolysis rate alternated by aerosol radiative influence,may affect O3 photochemistry under high aerosol loads.A three-dimensional air quality model,Models-3/Community Multi-scale Air Quality-Model of Aerosol Dynamics,Reaction,Ionization,and Dissolution,was employed to simulate the effects of the above-mentioned processes on O3 formation under typical high O3 episodes in Beijing during summer.Five heterogeneous reactions,i.e.,NO2,NO3,N2O5,HO2,and O3,were individually investigated to elucidate their effects on O3 formation.The results showed that the heterogeneous reactions significantly affected O3 formation in the urban plume.NO2 heterogeneous reaction increased O3 to 90 ppb,while HO2 heterogeneous reaction decreased O3 to 33 ppb.In addition,O3 heterogeneous loss decreased O3 to 31 ppb.The effects of NO2,NO3,and N2O5 heterogeneous reactions showed opposite O3 concentration changes between the urban and extra-urban areas because of the response of the reactions to the two types of O3 formation regimes.When the aerosol radiative influence was included,the photolysis rate decreased and O3 decreased significantly to 73 ppb O3.The two aerosol-related processes should be considered in the study of O3 formation because high aerosol concentration is a ubiquitous phenomenon that affects the urban- and regional air quality in China.

  18. Driving factors of aerosol concentration changes in the foothills of Central Himalayas

    Science.gov (United States)

    Kivekäs, Niku; Hooda, Rakesh; Hyvärinen, Antti-Pekka; Collaud-Coen, Martine; O'Connor, Ewan; Pietikäinen, Joni-Pekka; Backman, John; Vakkari, Ville; Lihavainen, Heikki

    2017-04-01

    Because of their short residence time in the atmosphere and uneven sources, the concentration, composition and properties of aerosol particles at a given location vary strongly depending on the air mass history and atmospheric mixing properties. Therefore detailed analysis is needed before a representative picture of the amount or composition of aerosol particles can be obtained. In this study we have analyzed 10 years (2005 - 2014) of aerosol data from Mukteshwar, a high-altitude site at 2180 m elevation in the foothills of Central Himalayas. The site is located on a mountain ridge with valleys on both sides. On larger scale the area consists of is low (peaks 1500 - 2500 m) mountains between the Gangetic Plains (100-200 m) and the actual Himalayas (peaks 6000 - 8000 m). The site is located in monsoon climate with most of the annual precipitation falling during the monsoon months (July and August). The data includes a variety of physical and optical properties of aerosols. We have analyzed the data for diurnal, weekly, and annual cycles, and for inter-annual variability and trends. We have also tried to identify the driving factors behind these changes. There were clear diurnal cycles in aerosol particle concentrations during all seasons apart for monsoon. All external aerosol parameters showed 1.5 - 2 times higher values during afternoon than during night time. This was linked to the diurnal pattern of turbulent mixing layer height, bringing polluted air from the valleys to the site. The timing of the pattern was consistent with increased turbulence, increased water vapor concentration in the air and change of wind direction at the site. The aerosol internal properties did not show a clear diurnal cycle. There were some weak indications of a weekday-weekend cycle during some months for some aerosol parameters, but no consistent patterns were found. The seasonal cycles of all external aerosol parameters were very clear. Every year the monsoon rains removed most of

  19. Direct gravimetric determination of aerosol mass concentration in central antarctica.

    Science.gov (United States)

    Annibaldi, Anna; Truzzi, Cristina; Illuminati, Silvia; Scarponi, Giuseppe

    2011-01-01

    In Antarctica, experimental difficulties due to extreme conditions have meant that aerosol mass has rarely been measured directly by gravimetry, and only in coastal areas where concentrations were in the range of 1-7 μg m(-3). The present work reports on a careful differential weighing methodology carried out for the first time on the plateau of central Antarctica (Dome C, East Antarctica). To solve problems of accurate aerosol mass measurements, a climatic room was used for conditioning and weighing filters. Measurements were carried out in long stages of several hours of readings with automatic recording of temperature/humidity and mass. This experimental scheme allowed us to sample from all the measurements (up to 2000) carried out before and after exposure, those which were recorded under the most stable humidity conditions and, even more importantly, as close to each other as possible. The automatic reading of the mass allowed us in any case to obtain hundreds of measurements from which to calculate average values with uncertainties sufficiently low to meet the requirements of the differential weighing procedure (±0.2 mg in filter weighing, between ±7% and ±16% both in aerosol mass and concentration measurements). The results show that the average summer aerosol mass concentration (aerodynamic size ≤10 μm) in central Antarctica is about 0.1 μg m(-3), i.e., about 1/10 of that of coastal Antarctic areas. The concentration increases by about 4-5 times at a site very close to the station.

  20. Aerosol classification by airborne high spectral resolution lidar observations

    Science.gov (United States)

    Groß, S.; Esselborn, M.; Weinzierl, B.; Wirth, M.; Fix, A.; Petzold, A.

    2013-03-01

    During four aircraft field experiments with the DLR research aircraft Falcon in 1998 (LACE), 2006 (SAMUM-1) and 2008 (SAMUM-2 and EUCAARI), airborne High Spectral Resolution Lidar (HSRL) and in situ measurements of aerosol microphysical and optical properties were performed. Altogether, the properties of six different aerosol types and aerosol mixtures - Saharan mineral dust, Saharan dust mixtures, Canadian biomass burning aerosol, African biomass burning mixture, anthropogenic pollution aerosol, and marine aerosol have been studied. On the basis of this extensive HSRL data set, we present an aerosol classification scheme which is also capable to identify mixtures of different aerosol types. We calculated mixing lines that allowed us to determine the contributing aerosol types. The aerosol classification scheme was supported by backward trajectory analysis and validated with in-situ measurements. Our results demonstrate that the developed aerosol mask is capable to identify complex stratifications with different aerosol types throughout the atmosphere.

  1. Influences of in-cloud aerosol scavenging parameterizations on aerosol concentrations and wet deposition in ECHAM5-HAM

    Directory of Open Access Journals (Sweden)

    B. Croft

    2009-10-01

    Full Text Available A diagnostic nucleation scavenging scheme, which determines stratiform cloud scavenging ratios for both aerosol mass and number distributions, based on cloud droplet, and ice crystal number concentrations, is introduced into the ECHAM5-HAM global climate model. This is coupled with a size-dependent in-cloud impaction scavenging parameterization for both cloud droplet-aerosol, and ice crystal-aerosol collisions. Sensitivity studies are presented, which compare aerosol concentrations, and deposition between a variety of in-cloud scavenging approaches, including prescribed fractions, several diagnostic schemes, and a prognostic aerosol cloud processing treatment that passes aerosol in-droplet and in-ice crystal concentrations between model time steps. For one sensitivity study, assuming 100% of the in-cloud aerosol is scavenged into the cloud droplets and ice crystals, the annual global mean accumulation mode number burden is decreased by 65%, relative to a simulation with prognostic aerosol cloud processing. Diagnosing separate nucleation scavenging ratios for aerosol number and mass distributions, as opposed to equating the aerosol mass scavenging to the number scavenging ratios, reduces the annual global mean sulfate burden by near to 10%. The annual global mean sea salt burden is 30% lower for the diagnostic approach, which does not carry aerosol in-droplet and in-crystal concentrations between model time-steps as compared to the prognostic scheme. Implementation of in-cloud impaction scavenging reduced the annual, global mean black carbon burden by 30% for the prognostic aerosol cloud processing scheme. Better agreement with observations of black carbon profiles from aircraft (changes near to one order of magnitude for mixed phase clouds, 210Pb surface layer concentrations and wet deposition, and the geographic distribution of aerosol optical depth are found for the new diagnostic scavenging as compared to prescribed ratio

  2. ACTRIS ACSM intercomparison - Part I: Reproducibility of concentration and fragment results from 13 individual Quadrupole Aerosol Chemical Speciation Monitors (Q-ACSM) and consistency with Time-of-Flight ACSM (ToF-ACSM), High Resolution ToF Aerosol Mass Spectrometer (HR-ToF-AMS) and other co-located instruments

    Science.gov (United States)

    Crenn, V.; Sciare, J.; Croteau, P. L.; Verlhac, S.; Fröhlich, R.; Belis, C. A.; Aas, W.; Äijälä, M.; Alastuey, A.; Artiñano, B.; Baisnée, D.; Bonnaire, N.; Bressi, M.; Canagaratna, M.; Canonaco, F.; Carbone, C.; Cavalli, F.; Coz, E.; Cubison, M. J.; Esser-Gietl, J. K.; Green, D. C.; Gros, V.; Heikkinen, L.; Herrmann, H.; Lunder, C.; Minguillón, M. C.; Močnik, G.; O'Dowd, C. D.; Ovadnevaite, J.; Petit, J.-E.; Petralia, E.; Poulain, L.; Priestman, M.; Riffault, V.; Ripoll, A.; Sarda-Estève, R.; Slowik, J. G.; Setyan, A.; Wiedensohler, A.; Baltensperger, U.; Prévôt, A. S. H.; Jayne, J. T.; Favez, O.

    2015-07-01

    As part of the European ACTRIS project, the first large Quadrupole Aerosol Chemical Speciation Monitor (Q-ACSM) intercomparison study was conducted in the region of Paris for three weeks during the late fall-early winter period (November-December 2013). The first week was dedicated to tuning and calibration of each instrument whereas the second and third were dedicated to side-by-side comparison in ambient conditions with co-located instruments providing independent information on submicron aerosol optical, physical and chemical properties. Near real-time measurements of the major chemical species (organic matter, sulfate, nitrate, ammonium and chloride) in the non-refractory submicron aerosols (NR-PM1) were obtained here from 13 Q-ACSM. The results show that these instruments can produce highly comparable and robust measurements of the NR-PM1 total mass and its major components. Taking the median of the 13 Q-ACSM as a reference for this study, strong correlations (r2 > 0.9) were observed systematically for each individual ACSM across all chemical families except for chloride for which three ACSMs showing weak correlations partly due to the very low concentrations during the study. Reproducibility expanded uncertainties of Q-ACSM concentration measurements were determined using appropriate methodologies defined by the International Standard Organization (ISO 17025) and were found to be of 9, 15, 19, 28 and 36 % for NR-PM1, nitrate, organic matter, sulfate and ammonium respectively. However, discrepancies were observed in the relative concentrations of the constituent mass fragments for each chemical component. In particular, significant differences were observed for the organic fragment at mass-to-charge ratio 44, which is a key parameter describing the oxidation state of organic aerosol. Following this first major intercomparison exercise of a large number of ACSMs, detailed intercomparison results are presented as well as a discussion of some recommendations

  3. Theoretical Basis for Convective Invigoration due to Increased Aerosol Concentration

    Science.gov (United States)

    Lebo, Z. J.; Chen, Y.; Seinfeld, J.

    2010-12-01

    Recent reports using a one-dimensional parcel model suggest that increases in aerosol number concentration may invigorate deep convection by mitigating the autoconversion process until air parcels reach the freezing level. This would lead to an increase in ice water aloft and the potential for enhanced upward heat transport due to phase changes, hence leading to invigorated convection. Other studies have proposed that an increase in aerosol loading may act to increase cloud top height, increasing the liquid water content, which ultimately increases the cumulative precipitation. Here we study the effect of aerosol perturbations on deep convection by employing the Weather Research and Forecasting model as a three-dimensional CRM with a two-moment, six-class bulk microphysics scheme. These results are corroborated using a newly developed bin microphysics scheme. The bulk microphysics scheme is augmented with a state-of-the-art activation scheme based on Köhler Theory and Population Splitting to analyze the effect of CCN perturbations on cloud development. Moreover, we include a physically-based parameterization for homogeneous and heterogeneous freezing to determine the effects of changes in IN number concentration on deep convective cloud development. We perform idealized simulations of deep convection over a wide range of CCN concentrations (i.e., 102 to 103 cm-3), which encompasses clean maritime conditions to polluted continental conditions, respectively. The detailed model calculations reveal that the CCN effect on precipitation in deep convective clouds depends strongly on the ambient water vapor mixing ratio profile. Our simulations suggest that under relatively dry conditions, an increase in aerosol number concentration leads to a decrease in precipitation (-4.2%), while under moist conditions, an increase in aerosol number concentration leads to an increase in precipitation (8.1%). However, when the water vapor in the mid- to upper-troposphere is depleted

  4. Amazon boundary layer aerosol concentration sustained by vertical transport during rainfall

    Science.gov (United States)

    Wang, Jian; Krejci, Radovan; Giangrande, Scott; Kuang, Chongai; Barbosa, Henrique M. J.; Brito, Joel; Carbone, Samara; Chi, Xuguang; Comstock, Jennifer; Ditas, Florian; Lavric, Jost; Manninen, Hanna E.; Mei, Fan; Moran-Zuloaga, Daniel; Pöhlker, Christopher; Pöhlker, Mira L.; Saturno, Jorge; Schmid, Beat; Souza, Rodrigo A. F.; Springston, Stephen R.; Tomlinson, Jason M.; Toto, Tami; Walter, David; Wimmer, Daniela; Smith, James N.; Kulmala, Markku; Machado, Luiz A. T.; Artaxo, Paulo; Andreae, Meinrat O.; Petäjä, Tuukka; Martin, Scot T.

    2016-11-01

    The nucleation of atmospheric vapours is an important source of new aerosol particles that can subsequently grow to form cloud condensation nuclei in the atmosphere. Most field studies of atmospheric aerosols over continents are influenced by atmospheric vapours of anthropogenic origin (for example, ref. 2) and, in consequence, aerosol processes in pristine, terrestrial environments remain poorly understood. The Amazon rainforest is one of the few continental regions where aerosol particles and their precursors can be studied under near-natural conditions, but the origin of small aerosol particles that grow into cloud condensation nuclei in the Amazon boundary layer remains unclear. Here we present aircraft- and ground-based measurements under clean conditions during the wet season in the central Amazon basin. We find that high concentrations of small aerosol particles (with diameters of less than 50 nanometres) in the lower free troposphere are transported from the free troposphere into the boundary layer during precipitation events by strong convective downdrafts and weaker downward motions in the trailing stratiform region. This rapid vertical transport can help to maintain the population of particles in the pristine Amazon boundary layer, and may therefore influence cloud properties and climate under natural conditions.

  5. Amazon boundary layer aerosol concentration sustained by vertical transport during rainfall.

    Science.gov (United States)

    Wang, Jian; Krejci, Radovan; Giangrande, Scott; Kuang, Chongai; Barbosa, Henrique M J; Brito, Joel; Carbone, Samara; Chi, Xuguang; Comstock, Jennifer; Ditas, Florian; Lavric, Jost; Manninen, Hanna E; Mei, Fan; Moran-Zuloaga, Daniel; Pöhlker, Christopher; Pöhlker, Mira L; Saturno, Jorge; Schmid, Beat; Souza, Rodrigo A F; Springston, Stephen R; Tomlinson, Jason M; Toto, Tami; Walter, David; Wimmer, Daniela; Smith, James N; Kulmala, Markku; Machado, Luiz A T; Artaxo, Paulo; Andreae, Meinrat O; Petäjä, Tuukka; Martin, Scot T

    2016-11-17

    The nucleation of atmospheric vapours is an important source of new aerosol particles that can subsequently grow to form cloud condensation nuclei in the atmosphere. Most field studies of atmospheric aerosols over continents are influenced by atmospheric vapours of anthropogenic origin (for example, ref. 2) and, in consequence, aerosol processes in pristine, terrestrial environments remain poorly understood. The Amazon rainforest is one of the few continental regions where aerosol particles and their precursors can be studied under near-natural conditions, but the origin of small aerosol particles that grow into cloud condensation nuclei in the Amazon boundary layer remains unclear. Here we present aircraft- and ground-based measurements under clean conditions during the wet season in the central Amazon basin. We find that high concentrations of small aerosol particles (with diameters of less than 50 nanometres) in the lower free troposphere are transported from the free troposphere into the boundary layer during precipitation events by strong convective downdrafts and weaker downward motions in the trailing stratiform region. This rapid vertical transport can help to maintain the population of particles in the pristine Amazon boundary layer, and may therefore influence cloud properties and climate under natural conditions.

  6. Coarse mode aerosols in the High Arctic

    Science.gov (United States)

    Baibakov, K.; O'Neill, N. T.; Chaubey, J. P.; Saha, A.; Duck, T. J.; Eloranta, E. W.

    2014-12-01

    Fine mode (submicron) aerosols in the Arctic have received a fair amount of scientific attention in terms of smoke intrusions during the polar summer and Arctic haze pollution during the polar winter. Relatively little is known about coarse mode (supermicron) aerosols, notably dust, volcanic ash and sea salt. Asian dust is a regular springtime event whose optical and radiative forcing effects have been fairly well documented at the lower latitudes over North America but rarely reported for the Arctic. Volcanic ash, whose socio-economic importance has grown dramatically since the fear of its effects on aircraft engines resulted in the virtual shutdown of European civil aviation in the spring of 2010 has rarely been reported in the Arctic in spite of the likely probability that ash from Iceland and the Aleutian Islands makes its way into the Arctic and possibly the high Arctic. Little is known about Arctic sea salt aerosols and we are not aware of any literature on the optical measurement of these aerosols. In this work we present preliminary results of the combined sunphotometry-lidar analysis at two High Arctic stations in North America: PEARL (80°N, 86°W) for 2007-2011 and Barrow (71°N,156°W) for 2011-2014. The multi-years datasets were analyzed to single out potential coarse mode incursions and study their optical characteristics. In particular, CIMEL sunphotometers provided coarse mode optical depths as well as information on particle size and refractive index. Lidar measurements from High Spectral Resolution lidars (AHSRL at PEARL and NSHSRL at Barrow) yielded vertically resolved aerosol profiles and gave an indication of particle shape and size from the depolarization ratio and color ratio profiles. Additionally, we employed supplementary analyses of HYSPLIT backtrajectories, OMI aerosol index, and NAAPS (Navy Aerosol Analysis and Prediction System) outputs to study the spatial context of given events.

  7. Vertical distribution characteristics of dust aerosol mass concentration in the Taklimakan Desert hinterland

    Institute of Scientific and Technical Information of China (English)

    XinChun Liu; YuTing Zhong; Qing He; XingHua Yang; Ali Mamtimin; Wen Huo

    2013-01-01

    The different height mass concentrations of dust aerosol data from the atmosphere environment observation station (Ta-zhong Station) was continuously observed by instruments of Grimm 1.108, Thermo RP 1400a and TSP from January of 2009 to February of 2010 in the Taklimakan Desert hinterland. Results show that:(1) The mass concentration value of 80 m PM10 was higher, but PM2.5 and PM1.0 concentrations at 80 m was obviously lower than 4 m PM10, and the value of 80 m PM1.0 mass concentration was the lowest. (2) The PM mass concentrations gradually decreased from night to sunrise, with the lowest concentration at 08:00, with the mass concentration gradually increased, up to the highest concentration around 18:00, and then decreased again. It was exactly the same with the changes of wind speed. (3) The high monthly average mass concentration of TSP mainly appeared from March to September, and the highest concentration was in April and May, subsequently gradually decreased. Also, March-September was a period with high value area of PM monthly average mass concentration, with the highest monthly average mass concentration of 846.0μg/m3 for 4 m PM10 appeared in May. The concentration of PM10 was much higher than those of PM2.5 and PM1.0 at 80 m. There is a small difference between the concentration of PM2.5 and PM1.0. Dust weather was the main factor which influenced the concentration content of the different diameter dust aerosol, and the more dust weather days, the higher content of coarse particle, conversely, fine particle was more. (4) The mass concentration of different diameter aerosols had the following sequence during dust weather: clear day < blowing dust < floating and blowing dust < sandstorm. In different dust weather, the value of PM10/TSP in fine weather was higher than that in floating weather, and much higher than those in blowing dust and sandstorm weather. (5) During the dust weather process, dust aerosol concentration gradually decreased with particle

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

    Science.gov (United States)

    Burton, S. P.; Ferrare, R. A.; Omar, A. H.; Hostetler, C. A.; Hair, J. W.; Rogers, R.; Obland, M. D.; Butler, C. F.; Cook, A. L.; Harper, D. B.

    2012-12-01

    The NASA Langley Research Center (LaRC) airborne High Spectral Resolution Lidar (HSRL-1) on the NASA B200 aircraft has acquired large datasets of aerosol extinction (532nm), backscatter (532 and 1064nm), and depolarization (532 and 1064nm) profiles during 349 science flights in 19 field missions across North America since 2006. The extinction-to-backscatter ratio ("lidar ratio"), aerosol depolarization ratios, and backscatter color ratio measurements from HSRL-1 are scale-invariant parameters that depend on aerosol type but not concentration. These four aerosol intensive parameters are combined to qualitatively classify HSRL aerosol measurements into eight separate composition types. The classification methodology uses models formed from "training cases" with known aerosol type. The remaining measurements are then compared with these models using the Mahalanobis distance. Aerosol products from the CALIPSO satellite include aerosol type information as well, which is used as input to the CALIPSO aerosol retrieval. CALIPSO aerosol types are inferred using a mix of aerosol loading-dependent parameters, estimated aerosol depolarization, and location, altitude, and surface type information. The HSRL instrument flies beneath the CALIPSO satellite orbit track, presenting the opportunity for comparisons between the HSRL aerosol typing and the CALIPSO Vertical Feature Mask Aerosol Subtype product, giving insight into the performance of the CALIPSO aerosol type algorithm. We find that the aerosol classification from the two instruments frequently agree for marine aerosols and pure dust, and somewhat less frequently for pollution and smoke. In addition, the comparison suggests that the CALIPSO polluted dust type is overly inclusive, encompassing cases of dust combined with marine aerosol as well as cases without much evidence of dust. Qualitative classification of aerosol type combined with quantitative profile measurements of aerosol backscatter and extinction has many useful

  9. Constructing An Event Based Aerosol Product Under High Aerosol Loading Conditions

    Science.gov (United States)

    Levy, R. C.; Shi, Y.; Mattoo, S.; Remer, L. A.; Zhang, J.

    2016-12-01

    High aerosol loading events, such as the Indonesia's forest fire in Fall 2015 or the persistent wintertime haze near Beijing, gain tremendous interests due to their large impact on regional visibility and air quality. Understanding the optical properties of these events and further being able to simulate and predict these events are beneficial. However, it is a great challenge to consistently identify and then retrieve aerosol optical depth (AOD) from passive sensors during heavy aerosol events. Some reasons include:1). large differences between optical properties of high-loading aerosols and those under normal conditions, 2) spectral signals of optically thick aerosols can be mistaken with surface depending on aerosol types, and 3) Extremely optically thick aerosol plumes can also be misidentified as clouds due to its high optical thickness. Thus, even under clear-sky conditions, the global distribution of extreme aerosol events is not well captured in datasets such as the MODIS Dark-Target (DT) aerosol product. In this study, with the synthetic use of OMI Aerosol Index, MODIS cloud product, and operational DT product, the heavy smoke events over the seven sea region are identified and retrieved over the dry season. An event based aerosol product that would compensate the standard "global" aerosol retrieval will be created and evaluated. The impact of missing high AOD retrievals on the regional aerosol climatology will be studied using this newly developed research product.

  10. Variations of the aerosol concentration and chemical composition over the arid steppe zone of Southern Russia in summer

    Science.gov (United States)

    Artamonova, M. S.; Gubanova, D. P.; Iordanskii, M. A.; Lebedev, V. A.; Maksimenkov, L. O.; Minashkin, V. M.; Obvintsev, Y. I.; Chketiani, O. G.

    2016-12-01

    Variations in the surface aerosol over the arid steppe zone of Southern Russia have been measured. The parameters of atmospheric aerosol (mass concentration, both dispersed and elemental compositions) and meteorological parameters were measured in Tsimlaynsk raion (Rostov oblast). The chemical composition of aerosol particles in the atmospheric surface layer has been determined, and the coefficients of enrichment of elements with respect to clarkes in the Earth's crust have been calculated. It is shown that, in summer, arid aerosols are transported from both alkaline and sandy soils of Kalmykia to the air basin over the observation zone. Aerosol particles in the surface air layer over this region have been found to contain the products of combustion of oil, coal, and ethylized fuel. These combustion products make a small contribution to the total mass concentration of atmospheric aerosol; however, they are most hazardous to the health of people because of their sizes and heavy-metal contents. A high concentration of submicron sulfur-containing aerosol particles of chemocondensation nature has been recorded. Sources of aerosol of both natural and anthropogenic origins in southern Russia are discussed.

  11. ModelE2-TOMAS development and evaluation using aerosol optical depths, mass and number concentrations

    Directory of Open Access Journals (Sweden)

    Y. H. Lee

    2014-09-01

    Full Text Available The TwO-Moment Aerosol Sectional microphysics model (TOMAS has been integrated into the state-of-the-art general circulation model, GISS ModelE2. TOMAS has the flexibility to select a size resolution as well as the lower size cutoff. A computationally efficient version of TOMAS is used here, which has 15 size bins covering 3 nm to 10 μm aerosol dry diameter. For each bin, it simulates the total aerosol number concentration and mass concentrations of sulphate, pure elementary carbon (hydrophobic, mixed elemental carbon (hydrophilic, hydrophobic organic matter, hydrophilic organic matter, sea salt, mineral dust, ammonium, and aerosol-associated water. This paper provides a detailed description of the ModelE2-TOMAS model and evaluates the model against various observations including aerosol precursor gas concentrations, aerosol mass and number concentrations, and aerosol optical depths. Additionally, global budgets in ModelE2-TOMAS are compared with those of other global aerosol models, and the TOMAS model is compared to the default aerosol model in ModelE2, which is a bulk aerosol model. Overall, the ModelE2-TOMAS predictions are within the range of other global aerosol model predictions, and the model has a reasonable agreement with observations of sulphur species and other aerosol components as well as aerosol optical depth. However, ModelE2-TOMAS (as well as the bulk aerosol model cannot capture the observed vertical distribution of sulphur dioxide over the Pacific Ocean possibly due to overly strong convective transport. The TOMAS model successfully captures observed aerosol number concentrations and cloud condensation nuclei concentrations. Anthropogenic aerosol burdens in the bulk aerosol model running in the same host model as TOMAS (ModelE2 differ by a few percent to a factor of 2 regionally, mainly due to differences in aerosol processes including deposition, cloud processing, and emission parameterizations. Larger differences are found

  12. Correlation of black carbon aerosol and carbon monoxide concentrations measured in the high-altitude environment of Mt. Huangshan, Eastern China

    Directory of Open Access Journals (Sweden)

    X. L. Pan

    2011-02-01

    Full Text Available Understanding the relationship between black carbon (BC and carbon monoxide (CO will help improve BC emission inventories and the evaluation of global/regional climate forcing effects. In the present work, the BC (PM1 and CO mixing ratio was continuously measured at a~high-altitude background station on the summit of Mt Huangshan between 2006 and 2009. Annual mean BC concentration was 654.6 ± 633.4 ng m−3 with maxima in spring and autumn, when biomass was burned over a large area in Eastern China. The yearly averaged CO concentration was 446.4 ± 167.6 ppbv, and the increase in the CO concentration was greatest in the cold season, implying that the large-scale domestic coal/biofuel combustion for heating has an effect. The BC–CO relationship was found to have different seasonal features but strong positive correlation (R > 0.8. Back trajectory cluster analysis showed that the ΔBC/ΔCO ratio of plumes from the Yangtze River Delta region was 6.58 ± 0.96 ng m−3 ppbv−1, which is consistent with result from INTEX-B emission inventory. The ΔBC/ΔCO ratios for air masses from Northern, Central Eastern and Southern China were 5.2 ± 0.63, 5.65 ± 0.58 and 5.21 ± 0.93 ng m−3 ppbv−1, respectively. Over the whole observation period, the ΔBC/ΔCO ratio had unimodal diurnal variations and had a maximum during the day (09:00–17:00 LST and minimum at night (21:00–04:00 LST in spring, summer, autumn and winter, indicating the effects of the intrusion of clean air mass from the high troposphere. The case study combined with measurements of urban PM10 concentrations and satellite observations demonstrated that the ΔBC/ΔCO ratio for a plume of burning biomass was 12.4 ng m−3 ppbv−1 and that for urban plumes in Eastern China was 5.3 ± 0.53 ng m−3 ppbv−1. Transportation and industry were deemed as

  13. Concentrations, size distributions and temporal variations of fluorescent biological aerosol particles in southern tropical India

    Science.gov (United States)

    Valsan, Aswathy; Krishna R, Ravi; CV, Biju; Huffman, Alex; Poschl, Ulrich; Gunthe, Sachin

    2015-04-01

    Biological aerosols constitute a wide range of dead and alive biological materials and structures that are suspended in the atmosphere. They play an important role in the atmospheric physical, chemical and biological processes and health of living being by spread of diseases among humans, plants, and, animals. The atmospheric abundance, sources, physical properties of PBAPs as compared to non-biological aerosols, however, is poorly characterized. The Indian tropical region, where large fraction of the world's total population is residing, experiences a distinctive meteorological phenomenon by means of Indian Summer Monsoon (IMS). Thus, the properties and characteristics of biological aerosols are also expected to be very diverse over the Indian subcontinent depending upon the seasons. Here we characterize the number concentration and size distribution of Fluorescent Biological Aerosol Particles (FBAP) at a high altitude continental site, Munnar (10.09 N, 77.06 E; 1605 m asl) in South India during the South-West monsoon, which constitute around 80 percent of the annual rainfall in Munnar. Continuous three months measurements (from 01 June 2014 to 21 Aug 2104) FBAPs were carried out at Munnar using Ultra Violet Aerodynamic Particle Sizer (UVAPS) during IMS. The mean number and mass concentration of coarse FBAP averaged over the entire campaign was 1.7 x 10-2 cm-3 and 0.24 µg m-3 respectively, which corresponds to 2 percent and 6 percent of total aerosol particle number and mass concentration. In agreement to other previous measurements the number size distribution of FBAP also peaks at 3.2 micron indicating the strong presence of fungal spores. This was also supported by the Scanning Electron Microscopic analysis of bioaerosols on filter paper. They also displayed a strong diurnal cycle with maximum concentration occurring at early morning hours. During periods of heavy and continuous rain where the wind is consistently blowing from South-West direction it was

  14. Aircraft measurements of vertical and spatial distribution of aerosol concentration and size over different environments in India

    Science.gov (United States)

    Kumari B., Padma; S, Mahesh Kumar R.; R, Kulkarni J.; N, Goswami B.

    2010-05-01

    It is well known that atmospheric aerosols play a major role in climate change by directly scattering and absorbing the incoming and outgoing radiation as well as through modifying cloud properties, such as droplet size distribution and cloud lifetime. However, aerosol measurements, particularly their vertical distribution, are less and unevenly distributed around the globe. Cloud Aerosol Interactions and Precipitation Enhancement Experiment (CAIPEEX) is an Indian National program conducted by the Indian Institute of Tropical Meteorology (IITM), Pune, India, during summer monsoon season May-September 2009. Under CAIPEEX program, an instrumented aircraft has been used to study background aerosol along with cloud microphysical properties and their interactions over different parts of India. This experiment has been carried out for the first time in India. During CAIPEEX, PCASP (Passive Cavity aerosol Spectro Photometer) which measures aerosol concentrations in the size range 0.1 to 3 microns is operated in the aircraft over different parts of India viz., Pathankot (May), Hyderabad (June), Bengaluru (June-July), Bareilly (July-August), Guwahati (August- September) and Pune (September). The preliminary results suggest that aerosol vertical distribution is observed up to a maximum of 7.0 - 7.5 km, with high surface concentrations and enhanced layers at higher altitudes. During monsoon period also high concentrations are observed. The spatial distribution of aerosols along the flight track shows aerosol gradient from one place to another place. Also thick haze is observed near Himalayas during the month of May. The results at all the locations showed high aerosol concentrations in the size range of 0.1 to 0.3 microns, steep decreasing trend from 0.3 - 0.6 microns and less concentration from 0.6 to 3 microns. In the size range of 0.1 to 0.3 microns the concentrations varied from 100-10000 particles/cc. In-depth analysis of CAIPEEX data gives a clear picture of aerosol

  15. Strong sensitivity of aerosol concentrations to convective wet scavenging parameterizations in a global model

    Directory of Open Access Journals (Sweden)

    B. Croft

    2012-01-01

    Full Text Available This study examines the influences of assumptions in convective wet scavenging parameterizations on global climate model simulations of aerosol concentrations and wet deposition. To facilitate this study, an explicit representation of the uptake of aerosol mass and number into convective cloud droplets and ice crystals by the processes of activation, collisions, freezing and evaporation is introduced into the ECHAM5-HAM model. This development replaces the prescribed aerosol cloud-droplet-borne/ice-crystal-borne fractions of the standard model. Relative to the standard model, the more consistent treatment between convective aerosol-cloud microphysical processes yields a reduction of aerosol wet removal in mixed liquid and ice phase convective clouds by at least a factor of two, and the global, annual mean aerosol burdens are increased by at least 20%. Two limiting cases regarding the wet scavenging of entrained aerosols are considered. In the first case, aerosols entering convective clouds at their bases are the only aerosols that are scavenged into cloud droplets, and are susceptible to removal by convective precipitation formation. In the second case, aerosols that are entrained into the cloud above the cloud base layer can activate, can collide with existing cloud droplets and ice crystals, and can subsequently be removed by precipitation formation. The limiting case that allows aerosols entrained above cloud base to become cloud-droplet-borne and ice-crystal-borne reduces the annual and global mean aerosol burdens by 30% relative to the other limiting case, and yields the closest agreement with global aerosol optical depth retrievals, and black carbon vertical profiles from aircraft campaigns (changes of about one order of magntiude in the upper troposphere. Predicted convective cloud droplet number concentrations are doubled in the tropical middle troposphere when aerosols entrained above cloud base are allowed to activate. These results

  16. High resolution aerosol optical thickness retrieval over the Pearl River Delta region with improved aerosol modelling

    Institute of Scientific and Technical Information of China (English)

    WONG; ManSing; NICHOL; Janet; LEE; Kwon; Ho

    2009-01-01

    Aerosol retrieval algorithms for the MODerate Resolution Imaging Spectroradiometer (MODIS) have been developed to estimate aerosol and microphysical properties of the atmosphere, which help to address aerosol climatic issues at global scale. However, higher spatial resolution aerosol products for urban areas have not been well researched mainly due to the difficulty of differentiating aerosols from bright surfaces in urban areas. Here, a new aerosol retrieval algorithm using the MODIS 500 m resolution images is described, to retrieve aerosol properties over Hong Kong and the Pearl River Delta region. The rationale of our technique is to first estimate the aerosol reflectance by decomposing the top-of-atmosphere reflectance from surface reflectance and Rayleigh path reflectance. For the determination of surface reflectance, a modified Minimum Reflectance Technique (MRT) is used, and MRT images are computed for different seasons. A strong correlation is shown between the surface reflectance of MRT images and MODIS land surface reflectance products (MOD09), with a value of 0.9. For conversion of aerosol reflectance to Aerosol Optical Thickness (AOT), comprehensive Look Up Tables (LUT) are constructed, in which aerosol properties and sun-viewing geometry in the radiative transfer calculations are taken into account. Four aerosol types, namely mixed urban, polluted urban, dust, and heavy pollution, were derived using cluster analysis on three years of AERONET measurements in Hong Kong. Their aerosol properties were input for LUT calculation. The resulting 500 m AOT images are highly correlated (r = 0.89) with AERONET sunphotometer observations in Hong Kong. This study demonstrates the applicability of aerosol retrieval at fine resolution scale in urban areas, which can assist the study of aerosol loading distribution and the impact of localized and transient pollution on urban air quality. In addition, the MODIS 500 m AOT images can be used to study cross

  17. High resolution aerosol optical thickness retrieval over the Pearl River Delta region with improved aerosol modelling

    Institute of Scientific and Technical Information of China (English)

    WONG ManSing; NICHOL Janet; LEE Kwon Ho; LI ZhanQing

    2009-01-01

    Aerosol retrieval algorithms for the MODerate Resolution Imaging Spectroradiometer (MODIS) have been developed to estimate aerosol and microphysical properties of the atmosphere, which help to address aerosol climatic issues at global scale. However, higher spatial resolution aerosol products for urban areas have not been well researched mainly due to the difficulty of differentiating aerosols from bright surfaces in urban areas. Here, a new aerosol retrieval algorithm using the MODIS 500 m resolu-tion images is described, to retrieve aerosol properties over Hong Kong and the Pearl River Delta re-gion. The rationale of our technique is to first estimate the aerosol reflectance by decomposing the top-of-atmosphere reflectance from surface reflectance and Rayleigh path reflectance. For the deter-mination of surface reflectance, a modified Minimum Reflectance Technique (MRT) is used, and MRT images are computed for different seasons. A strong correlation is shown between the surface reflec-tance of MRT images and MODIS land surface reflectance products (MOD09), with a value of 0.9. For conversion of aerosol reflectance to Aerosol Optical Thickness (AOT), comprehensive Look Up Tables (LUT) are constructed, in which aerosol properties and sun-viewing geometry in the radiative transfer calculations are taken into account. Four aerosol types, namely mixed urban, polluted urban, dust, and heavy pollution, were derived using cluster analysis on three years of AERONET measurements in Hong Kong. Their aerosol properties were input for LUT calculation. The resulting 500 m AOT images are highly correlated (r=0.89) with AERONET sunphotometer observations in Hong Kong. This study demonstrates the applicability of aerosol retrieval at fine resolution scale in urban areas, which can assist the study of aerosol loading distribution and the impact of localized and transient pollution on urban air quality. In addition, the MODIS 500 m AOT images can be used to study cross

  18. Experiments on aerosol removal by high-pressure water spray

    Energy Technology Data Exchange (ETDEWEB)

    Corno, Ada del, E-mail: delcorno@rse-web.it [RSE, Power Generation Technologies and Materials Dept, via Rubattino 54, I-20134 Milano (Italy); Morandi, Sonia, E-mail: morandi@rse-web.it [RSE, Power Generation Technologies and Materials Dept, via Rubattino 54, I-20134 Milano (Italy); Parozzi, Flavio, E-mail: parozzi@rse-web.it [RSE, Power Generation Technologies and Materials Dept, via Rubattino 54, I-20134 Milano (Italy); Araneo, Lucio, E-mail: lucio.araneo@polimi.it [Politecnico di Milano, Department of Energy, via Lambruschini 4A, I-20156 Milano (Italy); CNR-IENI, via Cozzi 53, I-20125 Milano (Italy); Casella, Francesco, E-mail: francesco2.casella@mail.polimi.it [Politecnico di Milano, Department of Energy, via Lambruschini 4A, I-20156 Milano (Italy)

    2017-01-15

    Highlights: • Experimental research to measure the efficiency of high-pressure sprays in capturing aerosols if applied to a filtered containment venting system in case of severe accident. • Cloud of monodispersed SiO{sub 2} particles with sizes 0.5 or 1.0 μm and initial concentration in the range 2–90 mg/m{sup 3}. • Carried out in a chamber 0.5 × 1.0 m and 1.5 m high, with transparent walls equipped with a high pressure water spray with single nozzle. • Respect to low-pressure sprays, removal efficiency turned out significant: the half-life for 1 μm particles with a removal high-pressure spray system is orders of magnitude shorter than that with a low-pressure sprays system. - Abstract: An experimental research was managed in the framework of the PASSAM European Project to measure the efficiency of high-pressure sprays in capturing aerosols when applied to a filtered containment venting system in case of severe accident. The campaign was carried out in a purposely built facility composed by a scrubbing chamber 0.5 × 1.0 m and 1.5 m high, with transparent walls to permit the complete view of the aerosol removal process, where the aerosol was injected to form a cloud of specific particle concentration. The chamber was equipped with a high pressure water spray system with a single nozzle placed on its top. The test matrix consisted in the combination of water pressure injections, in the range 50–130 bar, on a cloud of monodispersed SiO{sub 2} particles with sizes 0.5 or 1.0 μm and initial concentration ranging between 2 and 99 mg/m{sup 3}. The spray was kept running for 2 min and the efficiency of the removal was evaluated, along the test time, using an optical particle sizer. With respect to low-pressure sprays, the removal efficiency turned out much more significant: the half-life for 1 μm particles with a removal high-pressure spray system is orders of magnitude shorter than that with a low-pressure spray system. The highest removal rate was

  19. Ben Macdhui High Altitude Trace Gas and Aerosol Transport Experiment

    CSIR Research Space (South Africa)

    Piketh, SJ

    1999-01-01

    Full Text Available The Ben Macdhui High Altitude Aerosol and Trace Gas Transport Experiment (BHATTEX) was started to characterize the nature and magnitude of atmospheric, aerosol and trace gas transport paths recirculation over and exiting from southern Africa...

  20. Ambient aerosol concentrations of sugars and sugar-alcohols at four different sites in Norway

    Directory of Open Access Journals (Sweden)

    K. E. Yttri

    2007-08-01

    Full Text Available Sugars and sugar-alcohols are demonstrated to be important constituents of the ambient aerosol water-soluble organic carbon fraction, and to be tracers for primary biological aerosol particles (PBAP. In the present study, levels of four sugars (fructose, glucose, sucrose, trehalose and three sugar-alcohols (arabitol, inositol, mannitol in ambient aerosols have been quantified using a novel HPLC/HRMS-TOF (High Performance Liquid Chromatography in combination with High Resolution Mass Spectrometry – Time of Flight method to assess the contribution of PBAP to PM>sub>10 and PM2.5. Samples were collected at four sites in Norway at different times of the year in order to reflect the various contributing sources and the spatial and seasonal variation of the selected compounds.

    Sugars and sugar-alcohols were present at all sites investigated, underlining the ubiquity of these highly polar organic compounds. The highest concentrations were reported for sucrose, reaching a maximum concentration of 320 ng m−3 in PM10 and 55 ng m−3 in PM2.5. The mean concentration of sucrose was up to 10 times higher than fructose, glucose and the dimeric sugar trehalose. The mean concentrations of the sugar-alcohols were typically lower, or equal, to that of the monomeric sugars and trehalose. Peak concentrations of arabitol and mannitol did not exceed 30 ng m−3 in PM10, and for PM2.5 all concentrations were below 6 ng m−3.

    Sugars and sugar-alcohols were associated primarily with coarse aerosols except during wintertime at the suburban site in Elverum, where a shift towards sub micron aerosols was observed. It is proposed that this shift was due to the intensive use of wood burning for residential heating at this site during winter, confirmed by high concurrent concentrations of levoglucosan. Elevated concentrations of sugars in PM2

  1. Aerosol Composition in the Los Angeles Basin Studied by High Resolution Aerosol Mass Spectrometry

    Science.gov (United States)

    Hayes, P. L.; Ortega, A. M.; Cubison, M.; Hu, W.; Toohey, D. W.; Flynn, J. H.; Grossberg, N.; Lefer, B. L.; Alvarez, S. L.; Rappenglueck, B.; Allan, J. D.; Taylor, J.; Holloway, J. S.; Gilman, J. B.; Kuster, W. C.; De Gouw, J. A.; Massoli, P.; Zhang, X.; Weber, R.; Zhao, Y.; Cliff, S. S.; Wexler, A. S.; Isaacman, G. A.; Worton, D. R.; Kreisberg, N. M.; Hering, S. V.; Goldstein, A. H.; Jimenez, J. L.

    2011-12-01

    Atmospheric aerosols impact climate and health, but their sources and composition are poorly understood. To address this knowledge gap, a high-resolution aerosol mass spectrometer (AMS) and complementary instrumentation were deployed during the 2010 CalNex campaign to characterize aerosol composition in the Los Angeles (LA) area. Total mass concentrations as well as the species concentrations measured by the AMS compare well with most other instruments. Nitrate dominates in the mornings, but its concentration is reduced in the afternoon when organic aerosols (OA) increase and dominate. The diurnal variations in concentrations are strongly influenced by emission transport from the source-rich western basin. The average OA to enhanced CO ratio increases with photochemical age from 25 to 80 μg m-3 ppm-1, which indicates significant secondary OA (SOA) production and that a large majority of OA is secondary in aged air. The ratio values are similar to those from Mexico City as well as New England and the Mid-Atlantic States. Positive matrix factorization (PMF) is used to assess the concentrations of different OA components. The major OA classes are oxygenated OA (OOA, a surrogate for total SOA), and hydrocarbon-like OA (HOA, a surrogate for primary combustion OA). Several subclasses of OA are identified as well including diesel-influenced HOA (DI-HOA) and non-diesel HOA. DI-HOA exhibits low concentrations on Sundays consistent with the well-known weekday/weekend effect in LA. PMF analysis finds that OOA is 67% of the total OA concentration. A strong correlation between OOA and Ox (O3 + NO2) concentrations is observed with a slope of 0.15 that suggests the production of fresh SOA in Pasadena. Plotting the OA elemental ratios in a Van Krevelen diagram (H:C vs. O:C) yields a slope of -0.6, which is less steep than that observed in Riverside during the SOAR-2005 campaign. The difference in slopes may be attributed to the highly oxidized HOA present in Pasadena that is

  2. 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.

  3. Influences of in-cloud aerosol scavenging parameterizations on aerosol concentrations and wet deposition in ECHAM5-HAM

    Directory of Open Access Journals (Sweden)

    B. Croft

    2010-02-01

    Full Text Available A diagnostic cloud nucleation scavenging scheme, which determines stratiform cloud scavenging ratios for both aerosol mass and number distributions, based on cloud droplet, and ice crystal number concentrations, is introduced into the ECHAM5-HAM global climate model. This scheme is coupled with a size-dependent in-cloud impaction scavenging parameterization for both cloud droplet-aerosol, and ice crystal-aerosol collisions. The aerosol mass scavenged in stratiform clouds is found to be primarily (>90% scavenged by cloud nucleation processes for all aerosol species, except for dust (50%. The aerosol number scavenged is primarily (>90% attributed to impaction. 99% of this impaction scavenging occurs in clouds with temperatures less than 273 K. Sensitivity studies are presented, which compare aerosol concentrations, burdens, and deposition for a variety of in-cloud scavenging approaches: prescribed fractions, a more computationally expensive prognostic aerosol cloud processing treatment, and the new diagnostic scheme, also with modified assumptions about in-cloud impaction and nucleation scavenging. Our results show that while uncertainties in the representation of in-cloud scavenging processes can lead to differences in the range of 20–30% for the predicted annual, global mean aerosol mass burdens, and near to 50% for accumulation mode aerosol number burden, the differences in predicted aerosol mass concentrations can be up to one order of magnitude, particularly for regions of the middle troposphere with temperatures below 273 K where mixed and ice phase clouds exist. Different parameterizations for impaction scavenging changed the predicted global, annual mean number removal attributed to ice clouds by seven-fold, and the global, annual dust mass removal attributed to impaction by two orders of magnitude. Closer agreement with observations of black carbon profiles from aircraft (increases near to one order of magnitude for mixed phase clouds

  4. The effect of sea ice loss on sea salt aerosol concentrations and the radiative balance in the Arctic

    Directory of Open Access Journals (Sweden)

    H. Struthers

    2010-11-01

    Full Text Available Understanding Arctic climate change requires knowledge of both the external and the local drivers of Arctic climate as well as local feedbacks within the system. An Arctic feedback mechanism relating changes in sea ice extent to an alteration of the emission of sea salt aerosol and the consequent change in radiative balance is examined. A set of idealized climate model simulations were performed to quantify the radiative effects of changes in sea salt aerosol emissions induced by prescribed changes in sea ice extent. The model was forced using sea ice concentrations consistent with present day conditions and projections of sea ice extent for 2100. Sea salt aerosol emissions increase in response to a decrease in sea ice, the model results showing an annual average increase in number emission over the polar cap (70–90° N of 86×106 m−2 s−1 (mass emission increase of 23 μg m−2 s−1. This in turn leads to an increase in the natural aerosol optical depth of approximately 23%. In response to changes in aerosol optical depth, the natural component of the aerosol direct forcing over the Arctic polar cap is estimated to be between −0.2 and −0.4 W m−2 for the summer months, which results in a negative feedback on the system. The model predicts that the change in first indirect aerosol effect (cloud albedo effect is approximately a factor of ten greater than the change in direct aerosol forcing although this result is highly uncertain due to the crude representation of Arctic clouds and aerosol-cloud interactions in the model. This study shows that both the natural aerosol direct and first indirect effects are strongly dependent on the surface albedo, highlighting the strong coupling between sea ice, aerosols, Arctic clouds and their radiative effects.

  5. Aerosol-Radiation Feedback and PM10 Air Concentrations Over Poland

    Science.gov (United States)

    Werner, Małgorzata; Kryza, Maciej; Skjøth, Carsten Ambelas; Wałaszek, Kinga; Dore, Anthony J.; Ojrzyńska, Hanna; Kapłon, Jan

    2017-02-01

    We have implemented the WRF-Chem model version 3.5 over Poland to quantify the direct and indirect feedback effects of aerosols on simulated meteorology and aerosol concentrations. Observations were compared with results from three simulations at high spatial resolutions of 5 × 5 km: (1) BASE—without any aerosol feedback effects; (2) DIR—with direct aerosol-radiative effects (3) INDIR—with direct and indirect aerosol-radiative effects. We study the overall effect during January 2011 as well as selected episodes of the highest differences in PM10 concentrations between the three simulations. For the DIR simulation, the decrease in monthly mean incoming solar radiation (SWDOWN) appears for the entire study area. It changes geographically, from about -8.0 to -2.0 W m-2, respectively for the southern and northern parts of the country. The highest changes do not correspond to the highest PM10 concentration. Due to the solar radiation changes, the surface mean monthly temperature (T2) decreases for 96 % of the area of Poland, but not more than 1.0 °C. Monthly mean PBLH changes by more than ±5 m for 53 % of the domain. Locally the differences in PBLH between the DIR and BASE are higher than ± 20 m. Due to the direct effect, for 84 % of the domain, the mean monthly PM10 concentrations increase by up to 1.9 µg m-3. For the INDIR simulation the spatial distribution of changes in incoming solar radiation as well as air temperature is similar to the DIR simulation. The decrease of SWDOWN is noticed for the entire domain and for 23 % of the domain is higher than -5.0 W m-2. The absolute differences of PBLH are slightly higher for INDIR than DIR but similarly distributed spatially. For daily episodes, the differences between the simulations are higher, both for meteorology and PM10 concentrations, and the pattern of changes is usually more complex. The results indicate the potential importance of the aerosol feedback effects on modelled meteorology and PM10

  6. Contribution of feldspar and marine organic aerosols to global ice nucleating particle concentrations

    Science.gov (United States)

    Vergara-Temprado, Jesús; Murray, Benjamin J.; Wilson, Theodore W.; O'Sullivan, Daniel; Browse, Jo; Pringle, Kirsty J.; Ardon-Dryer, Karin; Bertram, Allan K.; Burrows, Susannah M.; Ceburnis, Darius; DeMott, Paul J.; Mason, Ryan H.; O'Dowd, Colin D.; Rinaldi, Matteo; Carslaw, Ken S.

    2017-03-01

    Ice-nucleating particles (INPs) are known to affect the amount of ice in mixed-phase clouds, thereby influencing many of their properties. The atmospheric INP concentration changes by orders of magnitude from terrestrial to marine environments, which typically contain much lower concentrations. Many modelling studies use parameterizations for heterogeneous ice nucleation and cloud ice processes that do not account for this difference because they were developed based on INP measurements made predominantly in terrestrial environments without considering the aerosol composition. Errors in the assumed INP concentration will influence the simulated amount of ice in mixed-phase clouds, leading to errors in top-of-atmosphere radiative flux and ultimately the climate sensitivity of the model. Here we develop a global model of INP concentrations relevant for mixed-phase clouds based on laboratory and field measurements of ice nucleation by K-feldspar (an ice-active component of desert dust) and marine organic aerosols (from sea spray). The simulated global distribution of INP concentrations based on these two species agrees much better with currently available ambient measurements than when INP concentrations are assumed to depend only on temperature or particle size. Underestimation of INP concentrations in some terrestrial locations may be due to the neglect of INPs from other terrestrial sources. Our model indicates that, on a monthly average basis, desert dusts dominate the contribution to the INP population over much of the world, but marine organics become increasingly important over remote oceans and they dominate over the Southern Ocean. However, day-to-day variability is important. Because desert dust aerosol tends to be sporadic, marine organic aerosols dominate the INP population on many days per month over much of the mid- and high-latitude Northern Hemisphere. This study advances our understanding of which aerosol species need to be included in order to

  7. Contribution of feldspar and marine organic aerosols to global ice nucleating particle concentrations

    Energy Technology Data Exchange (ETDEWEB)

    Vergara-Temprado, Jesús; Murray, Benjamin J.; Wilson, Theodore W.; O& amp; apos; Sullivan, Daniel; Browse, Jo; Pringle, Kirsty J.; Ardon-Dryer, Karin; Bertram, Allan K.; Burrows, Susannah M.; Ceburnis, Darius; DeMott, Paul J.; Mason, Ryan H.; O& amp; apos; Dowd, Colin D.; Rinaldi, Matteo; Carslaw, Ken S.

    2017-01-01

    Ice-nucleating particles (INPs) are known to affect the amount of ice in mixed-phase clouds, thereby influencing many of their properties. The atmospheric INP concentration changes by orders of magnitude from terrestrial to marine environments, which typically contain much lower concentrations. Many modelling studies use parameterizations for heterogeneous ice nucleation and cloud ice processes that do not account for this difference because they were developed based on INP measurements made predominantly in terrestrial environments without considering the aerosol composition. Errors in the assumed INP concentration will influence the simulated amount of ice in mixed-phase clouds, leading to errors in top-of-atmosphere radiative flux and ultimately the climate sensitivity of the model. Here we develop a global model of INP concentrations relevant for mixed-phase clouds based on laboratory and field measurements of ice nucleation by K-feldspar (an ice-active component of desert dust) and marine organic aerosols (from sea spray). The simulated global distribution of INP concentrations based on these two species agrees much better with currently available ambient measurements than when INP concentrations are assumed to depend only on temperature or particle size. Underestimation of INP concentrations in some terrestrial locations may be due to the neglect of INPs from other terrestrial sources. Our model indicates that, on a monthly average basis, desert dusts dominate the contribution to the INP population over much of the world, but marine organics become increasingly important over remote oceans and they dominate over the Southern Ocean. However, day-to-day variability is important. Because desert dust aerosol tends to be sporadic, marine organic aerosols dominate the INP population on many days per month over much of the mid- and high-latitude Northern Hemisphere. This study advances our understanding of which aerosol species need to be included in order to

  8. Concentrations and fluxes of aerosol particles during the LAPBIAT measurement campaign in Värriö field station

    Directory of Open Access Journals (Sweden)

    T. M. Ruuskanen

    2007-01-01

    Full Text Available The LAPBIAT measurement campaign took place in the SMEAR I measurement station located in Eastern Lapland in the spring of 2003 between 26 April and 11 May. In this paper we describe the measurement campaign, concentrations and fluxes of aerosol particles, air ions and trace gases, paying special attention to an aerosol particle formation event broken by a polluted air mass approaching from industrial areas of Kola Peninsula, Russia. Aerosol particle number flux measurements show strong downward fluxes during that time. Concentrations of coarse aerosol particles were high for 1–2 days before the nucleation event (i.e. 28–29 April, very low immediately before and during the observed aerosol particle formation event (30 April and increased moderately from the moment of sudden break of the event. In general particle deposition measurements based on snow samples show the same changes. Measurements of the mobility distribution of air ions showed elevated concentrations of intermediate air ions during the particle formation event. We estimated the growth rates in the nucleation mode size range. For particles <10 nm, the growth rate increases with size on 30 April. Dispersion modelling made with model SILAM support the conclusion that the nucleation event was interrupted by an outbreak of sulphate-rich air mass in the evening of 30 April that originated from the industry at Kola Peninsula, Russia. The results of this campaign highlight the need for detailed research in atmospheric transport of air constituents for understanding the aerosol dynamics.

  9. Shipboard measurements of concentrations and properties of carbonaceous aerosols during ACE-2

    OpenAIRE

    2011-01-01

    Mass concentrations of total, organic and black carbon were derived by analyzing the supermicron and submicron aerosol fractions of shipboard collected samples in the easternAtlantic Ocean as part of the second Aerosol Characterization Experiment (ACE-2). These analyses were complemented by experiments intended to estimate the water-soluble fraction of the submicron carbonaceous material. Our results can be summarized as follows. Depending on the sample, between 35% and 80% of total aerosol c...

  10. Concentration Effects on the Thermophoresis of Aerosol Spheres.

    Science.gov (United States)

    Keh; Ho

    1999-08-01

    The thermophoretic motion of a homogeneous suspension of identical spherical particles of arbitrary thermal conductivity and surface properties is considered under conditions of small Knudsen, Peclet, and Reynolds numbers. The effects of interaction of the individual particles are taken into explicit account by employing a unit cell model which is known to provide good predictions for the sedimentation of monodisperse suspensions of spherical particles. The appropriate equations of conservation of energy and momentum are solved for each cell, in which a spherical particle is envisaged to be surrounded by a concentric shell of suspending fluid, and the thermophoretic migration velocity of the particle is calculated for various cases. Analytical expressions of this mean particle velocity are obtained in closed form as functions of the volume fraction of the particles. Comparisons between the ensemble-averaged thermophoretic velocity of a test particle in a dilute suspension and our cell-model results are made. A parallel analysis for the sedimentation of aerosol spheres is also presented. Copyright 1999 Academic Press.

  11. Carbonaceous aerosols on the south edge of the Tibetan Plateau: concentrations, seasonality and sources

    Directory of Open Access Journals (Sweden)

    Z. Cong

    2014-10-01

    Full Text Available To quantitatively evaluate the effect of carbonaceous aerosols on the south edge of the Tibetan Plateau, aerosol samples were collected weekly from August 2009 to July 2010 at Mt. Everest (Qomolangma Station for Atmospheric and Environmental Observation and Research, briefly QOMS, 28.36° N, 86.95° E, 4276 m a.s.l.. The samples were analyzed for organic carbon (OC, elemental carbon (EC, water-soluble organic carbon (WSOC and major ions. The average concentrations of OC, EC and WSOC were 1.43, 0.25 and 0.77 μg m−3, respectively. The concentration levels of OC and EC at QOMS are comparable to those at high elevation sites on the southern slopes of the Himalayas (Langtang and NCO-P, but three to six times lower than those at Manora Peak, India and Godavari, Nepal. Sulfate was the most abundant anion species followed by nitrate, accounting for 25 and 12% of total ionic mass, respectively. Ca2+ was the most abundant cation species (annual average of 0.88 μg m−3. The various aerosol compositions showed distinctive seasonality. The dust loading, represented by Ca2+ concentration, was relatively constant throughout the year. While OC, EC and other ionic species (NH4+, K+, NO3−, and SO42− exhibited a pronounced peak in the pre-monsoon period and a minimum in the monsoon season. Similar seasonal trends of aerosol composition were also reported previously from the southern slope of the Himalayas, such as Langtang and NCO-P. This phenomenon indicates that both slopes of Himalayas share a common atmospheric environment regime. The strong correlation of OC and EC in QOMS aerosols with K+ and levoglucosan indicates that they were mainly originated from biomass burning. The active fire spots observed by MODIS and their backward trajectories further demonstrate that in pre-monsoon season, agricultural and forest fires in the northern India and Nepal were most likely sources of carbonaceous aerosol at QOMS. In addition to large-scale atmospheric

  12. Aerosol chemistry over a high altitude station at northeastern Himalayas, India.

    Directory of Open Access Journals (Sweden)

    Abhijit Chatterjee

    Full Text Available BACKGROUND: There is an urgent need for an improved understanding of the sources, distributions and properties of atmospheric aerosol in order to control the atmospheric pollution over northeastern Himalayas where rising anthropogenic interferences from rapid urbanization and development is becoming an increasing concern. METHODOLOGY/PRINCIPAL FINDINGS: An extensive aerosol sampling program was conducted in Darjeeling (altitude approximately 2200 meter above sea level (masl, latitude 27 degrees 01'N and longitude 88 degrees 15'E, a high altitude station in northeastern Himalayas, during January-December 2005. Samples were collected using a respirable dust sampler and a fine dust sampler simultaneously. Ion chromatograph was used to analyze the water soluble ionic species of aerosol. The average concentrations of fine and coarse mode aerosol were found to be 29.5+/-20.8 microg m(-3 and 19.6+/-11.1 microg m(-3 respectively. Fine mode aerosol dominated during dry seasons and coarse mode aerosol dominated during monsoon. Nitrate existed as NH(4NO(3 in fine mode aerosol during winter and as NaNO(3 in coarse mode aerosol during monsoon. Gas phase photochemical oxidation of SO(2 during premonsoon and aqueous phase oxidation during winter and postmonsoon were the major pathways for the formation of SO(4(2- in the atmosphere. Long range transport of dust aerosol from arid regions of western India was observed during premonsoon. The acidity of fine mode aerosol was higher in dry seasons compared to monsoon whereas the coarse mode acidity was higher in monsoon compared to dry seasons. Biomass burning, vehicular emissions and dust particles were the major types of aerosol from local and continental regions whereas sea salt particles were the major types of aerosol from marine source regions. CONCLUSIONS/SIGNIFICANCE: The year-long data presented in this paper provide substantial improvements to the heretofore poor knowledge regarding aerosol chemistry over

  13. Gas-phase CO2 subtraction for improved measurements of the organic aerosol mass concentration and oxidation degree by an aerosol mass spectrometer.

    Science.gov (United States)

    Collier, S; Zhang, Q

    2013-12-17

    The Aerodyne aerosol mass spectrometer (AMS) has been widely used for real-time characterization of the size-resolved chemical composition of sub-micrometer aerosol particles. The first step in AMS sampling is the pre-concentration of aerosols while stripping away the gas-phase components, which contributes to the high sensitivity of this instrument. The strength of the instrument lies in particle phase measurement; however, ion signals generated from gas-phase species can influence the interpretation of the particle-phase chemistry data. Here, we present methods for subtracting the varying contributions of gas-phase carbon dioxide (CO2) in the AMS spectra of aerosol particles, which is critical for determining the mass concentration and oxygen-to-carbon (O/C) ratio of organic aerosol. This report gives details on the gaseous CO2 subtraction analysis performed on a high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS) data set acquired from sampling of fresh and diluted vehicle emissions. Three different methods were used: (1) collocated continuous gas-phase CO2 measurement coupled with periodic filter tests consisting of sampling the same particle-free air by the AMS and the CO2 analyzer, (2) positive matrix factorization (PMF) analysis to separate the gas- and particle-phase signals of CO2(+) at m/z 44, and (3) use of the particle time-of-flight (PTOF) size-resolved chemical information for separation of gas- and particle-phase signals at m/z 44. Our results indicate that these three different approaches yield internally consistent values for the gas/particle apportionment of m/z 44, but methods 2 and 3 require certain conditions to be met to yield reliable results. The methods presented are applicable to any situation where gas-phase components may influence the PM signal of interest.

  14. Hourly elemental concentrations in PM2.5 aerosols sampled simultaneously at urban background and road site during SAPUSS -diurnal variations and PMF receptor modelling

    NARCIS (Netherlands)

    Dall'Osto, M.; Querol, X.; Amato, F.; Karanasiou, A.; Lucarelli, F.; Nava, S.; Calzolai, G.; Chiari, M.

    2013-01-01

    Hourly-resolved aerosol chemical speciation data can be a highly powerful tool to determine the source origin of atmospheric pollutants in urban environments. Aerosol mass concentrations of seventeen elements (Na, Mg, Al, S, Cl, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Sr and Pb) were obtained by time

  15. Comparison of black carbon (BC) aerosols in two urban areas - concentrations and size distributions

    Science.gov (United States)

    Hitzenberger, R.; Tohno, S.

    In this study, the BC aerosol measured at two very different urban sites is compared in terms of concentration, seasonal variation, and size distribution. During a 14 month study, one impactor sample was performed each month on a day with typical meteorological conditions. One (Vienna) or three (Uji) filter samples were obtained during the sampling time of the impactors. BC concentration in both the filter and impactor samples was analyzed with an optical technique (integrating sphere technique), where a calibration curve obtained from commercial carbon black is used to convert the optical signal to BC mass. Gravimetric mass concentration was measured at both sites. The gravimetric mass size distribution was measured only in Vienna. At both sites, the yearly average of the BC concentration on the sampling days was around 5 μg m -3. In Vienna, some seasonal trend with high concentrations during the cold season was observed, while in Uji, no pronounced seasonal trend was found. The BC size distribution in Uji was distinctly bimodal in the submicron size range. Log-normal distributions were fitted through the impactor data. The average BC mass median diameters (MMD) of the two submicron modes were 0.15 and 0.39 μm. Each mode contained about the same amount of BC mass. In Vienna only one submicron BC mode (average MMD 0.3 μm) was found because of the low size resolution of the impactor. An analysis of humidity effects on the MMDs of BC (both sites) and gravimetric mass (Vienna only) indicates that the Vienna aerosol is partly mixed internally with respect to BC, while the Uji aerosol seems to be externally mixed.

  16. Single-particle characterization of the High Arctic summertime aerosol

    Directory of Open Access Journals (Sweden)

    B. Sierau

    2014-01-01

    Full Text Available Single-particle mass spectrometric measurements were carried out in the High Arctic north of 80° during summer 2008. The campaign took place onboard the icebreaker \\textit{Oden} and was part of the Arctic Summer Cloud Ocean Study (ASCOS. The instrument deployed was an Aerosol Time-of-Flight Mass Spectrometer (ATOFMS that provides information on the chemical composition of individual particles and their mixing state in real-time. Aerosols were sampled in the marine boundary layer at stations in the open ocean, in the marginal ice zone, and in the pack ice region. The largest fraction of particles detected for subsequent analysis in the size range of the ATOFMS between approximately 200 nm to 3000 nm in diameter showed mass spectrometric patterns indicating an internal mixing state and a biomass burning and/or biofuel source. The majority of these particles were connected to an air mass layer of elevated particle concentration mixed into the surface mixed layer from the upper part of the marine boundary layer. The second largest fraction was represented by sea salt particles. The chemical analysis of the over-ice sea salt aerosol revealed tracer compounds that reflect chemical aging of the particles during their long-range advection from the marginal ice zone, or open waters south thereof prior to detection at the ship. From our findings we conclude that long-range transport of particles is one source of aerosols in the High Arctic. To assess the importance of long-range particle sources for aerosol–cloud interactions over the inner Arctic in comparison to local and regional biogenic primary aerosol sources, the chemical composition of the detected particles was analyzed for indicators of marine biological origin. Only a~minor fraction showed chemical signatures of potentially ocean-derived primary particles of that kind. However, a chemical bias in the ATOFMS's detection capabilities observed during ASCOS might suggest a presence of a

  17. Susceptibility of Tribolium confusum (Coleoptera: Tenebrionidae) to Pyrethrin Aerosol: Effects of Aerosol Particle Size, Concentration, and Exposure Conditions.

    Science.gov (United States)

    Arthur, Frank H; Campbell, James F; Ducatte, Gerald R

    2014-12-01

    A series of laboratory studies was conducted to assess the effect of droplet size on efficacy of pyrethrin aerosol against adults of Tribolium confusum Jacqueline DuVal, the confused flour beetle. A vertical flow aerosol exposure chamber that generated a standardized particle size diameter was used for these trials. In the first experiments, adults were exposed in the chamber for 2.5-45 min to aerosol dispensed at a volumetric median particle size diameter (VMD) of 16 μm, and then held in the arenas in which they were exposed or transferred to new arenas with or without a flour food source. All adults were initially knocked down when removed from the chamber. Recovery from knockdown decreased as exposure interval increased, but the presence of a food source enhanced recovery at the lower exposure intervals. In the second experiment, the aerosol was applied at a VMD of 2 μm and adults were exposed for between 5 and 75 min. Knockdown of adults was ≤10% when adults were removed from the chamber regardless of exposure time and afterward there was essentially complete recovery of adults. In the third and final experiment, the same 2-μm VMD particle size and exposure times were used, but the concentration of aerosol was increased by ≍4× compared with the previous experiment. In this test, initial knockdown was greater at the higher exposure intervals, but by 3 and 4 d posttreatment, recovery was again essentially 100%. This is the first published test assessing the efficacy of specific aerosol particle sizes on a stored product insect. Results indicate that particle size was a more important factor in conferring toxicity than the actual concentration or number of aerosol particles. © 2014 Entomological Society of America.

  18. Artifacts in measuring aerosol uptake kinetics: the roles of time, concentration and adsorption

    Science.gov (United States)

    Renbaum, L. H.; Smith, G. D.

    2011-07-01

    In laboratory studies of organic aerosol particles reacting with gas-phase oxidants, high concentrations of radicals are often used to study on the timescale of seconds reactions which may be occurring over days or weeks in the troposphere. Implicit in this approach is the assumption that radical concentration and time are interchangeable parameters, though this has not been established. Here, the kinetics of OH- and Cl-initiated oxidation reactions of model single-component liquid (squalane) and supercooled (brassidic acid and 2-octyldodecanoic acid) organic aerosols are studied by varying separately the radical concentration and the reaction time. Two separate flow tubes with residence times of 2 and 66 s are used, and [OH] and [Cl] are varied by adjusting either the laser photolysis fluence or the radical precursor concentration ([O3] or [Cl2], respectively) used to generate the radicals. It is found that the rates measured by varying the radical concentration and the reaction time are equal only if the precursor concentrations are the same in the two approaches. Further, the rates depend on the concentrations of the precursor species with a Langmuir-type functional form suggesting that O3 and Cl2 saturate the surface of the liquid particles. It is believed that the presence of O3 inhibits the rate of OH reaction, perhaps by reacting with OH radicals or by O3 or intermediate species blocking surface sites, while Cl2 enhances the rate of Cl reaction by participating in a radical chain mechanism. These results have important implications for laboratory experiments in which high concentrations of gas-phase oxidants are used to study atmospheric reactions over short timescales and may explain the variability in recent measurements of the reactive uptake of OH on squalane particles in reactor systems used in this and other laboratories.

  19. Artifacts in measuring aerosol uptake kinetics: the roles of time, concentration and adsorption

    Directory of Open Access Journals (Sweden)

    L. H. Renbaum

    2011-07-01

    Full Text Available In laboratory studies of organic aerosol particles reacting with gas-phase oxidants, high concentrations of radicals are often used to study on the timescale of seconds reactions which may be occurring over days or weeks in the troposphere. Implicit in this approach is the assumption that radical concentration and time are interchangeable parameters, though this has not been established. Here, the kinetics of OH- and Cl-initiated oxidation reactions of model single-component liquid (squalane and supercooled (brassidic acid and 2-octyldodecanoic acid organic aerosols are studied by varying separately the radical concentration and the reaction time. Two separate flow tubes with residence times of 2 and 66 s are used, and [OH] and [Cl] are varied by adjusting either the laser photolysis fluence or the radical precursor concentration ([O3] or [Cl2], respectively used to generate the radicals. It is found that the rates measured by varying the radical concentration and the reaction time are equal only if the precursor concentrations are the same in the two approaches. Further, the rates depend on the concentrations of the precursor species with a Langmuir-type functional form suggesting that O3 and Cl2 saturate the surface of the liquid particles. It is believed that the presence of O3 inhibits the rate of OH reaction, perhaps by reacting with OH radicals or by O3 or intermediate species blocking surface sites, while Cl2 enhances the rate of Cl reaction by participating in a radical chain mechanism. These results have important implications for laboratory experiments in which high concentrations of gas-phase oxidants are used to study atmospheric reactions over short timescales and may explain the variability in recent measurements of the reactive uptake of OH on squalane particles in reactor systems used in this and other laboratories.

  20. Artifacts in measuring aerosol uptake kinetics: the roles of time, concentration and adsorption

    Directory of Open Access Journals (Sweden)

    L. H. Renbaum

    2011-03-01

    Full Text Available In laboratory studies of organic aerosol particles reacting with gas-phase oxidants, high concentrations of radicals are often used to study on the timescale of seconds reactions which may be occurring over days or weeks in the troposphere. Implicit in this approach is the assumption that radical concentration and time are interchangeable parameters, though this has not been established. Here, the kinetics of OH- and Cl-initiated oxidation reactions of model single-component liquid organic aerosols (squalane, brassidic acid and 2-octyldodecanoic acid are studied by varying separately the radical concentration and the reaction time. Two separate flow tubes with residence times of 2 and 66 s are used, and [OH] and [Cl] are varied by adjusting either the laser photolysis fluence or the radical precursor concentration ([O3] or [Cl2], respectively used to generate the radicals. It is found that the rates measured by varying the radical concentration and the reaction time are equal only if the precursor concentrations are the same in the two approaches. Further, the rates depend on the concentrations of the precursor species with a Langmuir-type functional form suggesting that O3 and Cl2 saturate the surface of the liquid particles. It is believed that the presence of O3 inhibits the rate of OH reaction, perhaps by reacting with OH radicals or blocking surface sites, while Cl2 enhances the rate of Cl reaction by participating in a radical chain mechanism. These results have important implications for laboratory experiments in which high concentrations of gas-phase oxidants are used to study atmospheric reactions over short timescales and may explain the variability in recent measurements of the reactive uptake of OH on squalane particles in reactor systems used in this and other laboratories.

  1. Indirect effect of changing aerosol concentrations on methane and ozone radiative forcing

    Science.gov (United States)

    Rowlinson, Matthew; Rap, Alexandru; Arnold, Steve; Forster, Piers; Chipperfield, Martyn

    2017-04-01

    % decreases atmospheric sulpate concentrations by 44% after 2 years, while increasing global OH concentrations by 0.9%. CH4 lifetime is reduced by approximately 50 days as a result, leading to a decrease in CH4 burden of 38ppb. NOx is anticipated to have a similar but much larger effect (Matsui and Koike 2016). The Edwards and Slingo offline radiation model is also used to calculate changes to direct and indirect aerosol forcing. Presented here is the net RF change following 50% emission decrease of each aerosol or precursors, accounting for the direct and indirect aerosol effect as well as indirect effects via oxidation chemistry on the RF due to CH4 and tropospheric O3.

  2. Hourly elemental concentrations in PM2.5 aerosols sampled simultaneously at urban background and road site

    Directory of Open Access Journals (Sweden)

    G. Calzolai

    2012-08-01

    Full Text Available Hourly-resolved aerosol chemical speciation data can be a highly powerful tool to determine the source origin of atmospheric pollutants in urban Environments. Aerosol mass concentrations of seventeen elements (Na, Mg, Al, S, Cl, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Sr and Pb were obtained by time (1 h and size (PM2.5 particulate matter 2.5 fraction simultaneously measured at the UB and RS sites: (1 the regional aerosol sources impact both monitoring sites at similar concentrations regardless their different ventilation conditions; (2 by contrast, local industrial aerosol plumes associated with shipping oil combustion and smelters activities have a higher impact on the more ventilated UB site; (3 a unique source of Pb-Cl (associated with industrial combustion emissions is found a to be the major (82% source of Cl in the urban agglomerate; (4 PM2.5 traffic brake dust (Fe-Cu is mainly primarily emitted and not resuspended, whereas PM2.5 urban crustal dust (Ca is found mainly resuspended by both traffic vortex and sea breeze; (5 urban dust (Ca is found the aerosol source most affected by land wetness, reduced by a factor of eight during rainy days and suggesting that wet roads may be a solution for reducing dust concentrations in road sites, far more effective than street sweeping activities.

  3. Effect of aerosols and NO2 concentration on ultraviolet actinic flux near Mexico City during MILAGRO: measurements and model calculations

    Science.gov (United States)

    Palancar, G. G.; Lefer, B. L.; Hall, S. R.; Shaw, W. J.; Corr, C. A.; Herndon, S. C.; Slusser, J. R.; Madronich, S.

    2013-01-01

    Urban air pollution absorbs and scatters solar ultraviolet (UV) radiation, and thus has a potentially large effect on tropospheric photochemical rates. We present the first detailed comparison between actinic fluxes (AF) in the wavelength range 330-420 nm measured in highly polluted conditions and simulated with the Tropospheric Ultraviolet-Visible (TUV) model. Measurements were made during the MILAGRO campaign near Mexico City in March 2006, at a ground-based station near Mexico City (the T1 supersite) and from the NSF/NCAR C-130 aircraft. At the surface, measured AF values are typically smaller than the model by up to 25% in the morning, 10% at noon, and 40% in the afternoon, for pollution-free and cloud-free conditions. When measurements of PBL height, NO2 concentration and aerosols optical properties are included in the model, the agreement improves to within ±10% in the morning and afternoon, and ±3% at noon. Based on daily averages, aerosols account for 68% and NO2 for 25% of AF reductions observed at the surface. Several overpasses from the C-130 aircraft provided the opportunity to examine the AF perturbations aloft, and also show better agreement with the model when aerosol and NO2 effects are included above and below the flight altitude. TUV model simulations show that the vertical structure of the actinic flux is sensitive to the choice of the aerosol single scattering albedo (SSA) at UV wavelengths. Typically, aerosols enhance AF above the PBL and reduce AF near the surface. However, for highly scattering aerosols (SSA > 0.95), enhancements can penetrate well into the PBL, while for strongly absorbing aerosols (SSA < 0.6) reductions in AF are computed in the free troposphere as well as in the PBL. Additional measurements of the SSA at these wavelengths are needed to better constrain the effect of aerosols on the vertical structure of the AF.

  4. Effect of aerosols and NO2 concentration on ultraviolet actinic flux near Mexico City during MILAGRO: measurements and model calculations

    Directory of Open Access Journals (Sweden)

    C. A. Corr

    2013-01-01

    Full Text Available Urban air pollution absorbs and scatters solar ultraviolet (UV radiation, and thus has a potentially large effect on tropospheric photochemical rates. We present the first detailed comparison between actinic fluxes (AF in the wavelength range 330–420 nm measured in highly polluted conditions and simulated with the Tropospheric Ultraviolet-Visible (TUV model. Measurements were made during the MILAGRO campaign near Mexico City in March 2006, at a ground-based station near Mexico City (the T1 supersite and from the NSF/NCAR C-130 aircraft. At the surface, measured AF values are typically smaller than the model by up to 25% in the morning, 10% at noon, and 40% in the afternoon, for pollution-free and cloud-free conditions. When measurements of PBL height, NO2 concentration and aerosols optical properties are included in the model, the agreement improves to within ±10% in the morning and afternoon, and ±3% at noon. Based on daily averages, aerosols account for 68% and NO2 for 25% of AF reductions observed at the surface. Several overpasses from the C-130 aircraft provided the opportunity to examine the AF perturbations aloft, and also show better agreement with the model when aerosol and NO2 effects are included above and below the flight altitude. TUV model simulations show that the vertical structure of the actinic flux is sensitive to the choice of the aerosol single scattering albedo (SSA at UV wavelengths. Typically, aerosols enhance AF above the PBL and reduce AF near the surface. However, for highly scattering aerosols (SSA > 0.95, enhancements can penetrate well into the PBL, while for strongly absorbing aerosols (SSA < 0.6 reductions in AF are computed in the free troposphere as well as in the PBL. Additional measurements of the SSA at these wavelengths are needed to better constrain the effect of aerosols on the vertical structure of the AF.

  5. Effect of aerosols and NO2 concentration on ultraviolet actinic flux near Mexico City during MILAGRO: measurements and model calculations

    Directory of Open Access Journals (Sweden)

    C. A. Corr

    2012-08-01

    Full Text Available Urban air pollution absorbs and scatters solar ultraviolet (UV radiation, and thus has a potentially large effect on tropospheric photochemical rates. We present the first detailed comparison between UV actinic fluxes (AF measured in highly polluted conditions and simulated with the Tropospheric Ultraviolet-Visible (TUV model. Measurements were made during the MILAGRO campaign near Mexico City in March 2006, at a ground-based station near Mexico City (the T1 supersite and from the NSF/NCAR C-130 aircraft. At the surface, measured AF values are typically smaller than the model by up to 25% in the morning, 10% at noon, and 40% in the afternoon, for pollution-free and cloud-free conditions. When measurements of PBL height, NO2 concentration and aerosols optical properties are included in the model, the agreement improves to within ±10% in the morning and afternoon, and ±3% at noon. Based on daily averages, aerosols account for 67% and NO2 for 25% of AF reductions observed at the surface. Several overpasses from the C-130 aircraft provided the opportunity to examine the AF perturbations aloft, and also show better agreement with the model when aerosol and NO2 effects are included above and below the flight altitude. TUV model simulations show that the vertical structure of the actinic flux is sensitive to the choice of the aerosol single scattering albedo (SSA at UV wavelengths. Typically, aerosols enhance AF above the PBL and reduce AF near the surface. However, for highly scattering aerosols (SSA > 0.95, enhancements can penetrate well into the PBL, while for strongly absorbing aerosols (SSA < 0.6 reductions in AF are computed in the free troposphere as well as in the PBL. Additional measurements of the SSA at these wavelengths are needed to better constrain the effect of aerosols on the vertical structure of the AF.

  6. Factors affecting the indoor concentrations of carbonaceous aerosols of outdoor origin

    Energy Technology Data Exchange (ETDEWEB)

    Lunden, Melissa M.; Kirchstetter, Thomas W.; Thatcher, Tracy L.; Hering, Susanne V.; Brown, Nancy J.

    2007-06-25

    A field study was conducted in an unoccupied single story residence in Clovis, California to provide data to address issues important to assess the indoor exposure to particles of outdoor origin. Measurements of black and organic carbonaceous aerosols were performed using a variety of methods, resulting in both near real-time measurements as well as integrated filter based measurements. Comparisons of the different measurement methods show that it is crucial to account for gas phase adsorption artifacts when measuring organic carbon (OC). Measured concentrations affected by the emissions of organic compounds sorbed to indoor surfaces imply a higher degree of infiltration of outdoor organic carbon aerosols into the indoor environment for our unoccupied house. Analysis of the indoor and outdoor data for black carbon (BC) aerosols show that, on average, the indoor concentration of black carbon aerosols behaves in a similar manner to sulfate aerosols. In contrast, organic carbon aerosols are subject to chemical transformations indoors that, for our unoccupied home, resulted in lower indoor OC concentrations than would be expected by physical loss mechanisms alone. These results show that gas to particle partitioning of organic compounds, as well as gas to surface interactions within the residence, are an important process governing the indoor concentration to OC aerosols of outdoor origin.

  7. Research Note Difference between low-volume and high-volume Andersen samplers in measuring atmospheric aerosols

    Institute of Scientific and Technical Information of China (English)

    Fengfu Fu; Nobuo Shinohaya; Mitsuo Ito; Xueqin Xu; Mincong Shen; Liangjun Xu

    2008-01-01

    The mass concentration and size distribution of aerosols in Tokaimura were investigated using a high-volume and a low-volume Andersen sampler. A difference was found using the two samplers: the concentration of total aerosols determined with the high-volume sampler is smaller than that of the low-volume sampler by 70-90% throughout the year. Compared to the high-volume sampler, low-volume sampler gave lower concentration for aerosols7μm, higher concentration for aerosols of 3.3-7.0μm and<1.1μm, though similar results for aerosols of 1.1-3.3μm. The low-volume sampler was found to have better separation efficiency and higher accuracy.

  8. Quantification of marine aerosol subgrid variability and its correlation with clouds based on high-resolution regional modeling: Quantifying Aerosol Subgrid Variability

    Energy Technology Data Exchange (ETDEWEB)

    Lin, Guangxing; Qian, Yun; Yan, Huiping; Zhao, Chun; Ghan, Steven J.; Easter, Richard C.; Zhang, Kai

    2017-06-16

    One limitation of most global climate models (GCMs) is that with the horizontal resolutions they typically employ, they cannot resolve the subgrid variability (SGV) of clouds and aerosols, adding extra uncertainties to the aerosol radiative forcing estimation. To inform the development of an aerosol subgrid variability parameterization, here we analyze the aerosol SGV over the southern Pacific Ocean simulated by the high-resolution Weather Research and Forecasting model coupled to Chemistry. We find that within a typical GCM grid, the aerosol mass subgrid standard deviation is 15% of the grid-box mean mass near the surface on a 1 month mean basis. The fraction can increase to 50% in the free troposphere. The relationships between the sea-salt mass concentration, meteorological variables, and sea-salt emission rate are investigated in both the clear and cloudy portion. Under clear-sky conditions, marine aerosol subgrid standard deviation is highly correlated with the standard deviations of vertical velocity, cloud water mixing ratio, and sea-salt emission rates near the surface. It is also strongly connected to the grid box mean aerosol in the free troposphere (between 2 km and 4 km). In the cloudy area, interstitial sea-salt aerosol mass concentrations are smaller, but higher correlation is found between the subgrid standard deviations of aerosol mass and vertical velocity. Additionally, we find that decreasing the model grid resolution can reduce the marine aerosol SGV but strengthen the correlations between the aerosol SGV and the total water mixing ratio (sum of water vapor, cloud liquid, and cloud ice mixing ratios).

  9. Winter monsoon variability and its impact on aerosol concentrations in East Asia.

    Science.gov (United States)

    Jeong, Jaein I; Park, Rokjin J

    2017-02-01

    We investigate the relationship between winter aerosol concentrations over East Asia and variability in the East Asian winter monsoon (EAWM) using GEOS-Chem 3-D global chemical transport model simulations and ground-based aerosol concentration data. We find that both observed and modeled surface aerosol concentrations have strong relationships with the intensity of the EAWM over northern (30-50°N, 100-140°E) and southern (20-30°N, 100-140°E) East Asia. In strong winter monsoon years, compared to weak winter monsoon years, lower and higher surface PM2.5 concentrations by up to 25% are shown over northern and southern East Asia, respectively. Analysis of the simulated results indicates that the southward transport of aerosols is a key process controlling changes in aerosol concentrations over East Asia associated with the EAWM. Variability in the EAWM is found to play a major role in interannual variations in aerosol concentrations; consequently, changes in the EAWM will be important for understanding future changes in wintertime air quality over East Asia. Copyright © 2016 Elsevier Ltd. All rights reserved.

  10. SEASONAL CHARACTERIZATION OF DUST DAYS,MASS CONCENTRATION AND DRY DEPOSITION OF ATMOSPHERIC AEROSOLS OVER QINGDAO, CHINA

    Institute of Scientific and Technical Information of China (English)

    Renjian Zhang; Mingxing Wang; Lifang Sheng; Yutaka Kanai; Atsuyuki Ohta

    2004-01-01

    The seasonal characterization of dust days, mass concentration and dry deposition of atmospheric aerosols were investigated using the historical data of dust days observed over Qingdao during the period from 1961 to 2001and ground-based aerosol sampling data collected in the period from May 2001 to November 2002. In Qingdao most of the dust days occurred in spring and in winter and no dust days existed in summer. The seasonal variation of the uplifting dust day over Qingdao was in phase with that analyzed over North China. The mean mass concentration of the total values and phase of the seasonal oscillation for fine particles were very similar to those for coarse particles except for the month March, during which the concentration of the coarse particles was about 4 times as high as that of the fine particles. Comparison between seasonal variation of mass concentration of aerosols and dust days indicated that high frequency of uplifting dust day was accompanied by high TSP mass concentration. The TSP mass concentration measured by the low-volume instrument was about 30% lower than that measured by high-volume instrument, though the two data sets are highly correlated (correlation coefficient=0.89). The dry deposition flux during the observation period from as that over Beijing.

  11. Development of a high-spectral-resolution lidar for continuous observation of aerosols in South America

    Science.gov (United States)

    Jin, Yoshitaka; Sugimoto, Nobuo; Nishizawa, Tomoaki; Ristori, Pablo; Papandrea, Sebastian; Otero, Lidia; Quel, Eduardo; Mizuno, Akira

    2016-05-01

    Continuous monitoring of aerosol profiles using lidar is helpful for a quasi-real-time indication of aerosol concentration. For instance, volcanic ash concentration and its height distribution are essential information for plane flights. Depolarization ratio and multi-wavelength measurements are useful for characterizing aerosol types such as volcanic ash, smoke, dust, sea-salt, and air pollution aerosols. High spectral resolution lidar (HSRL) and Raman scattering lidar can contribute to such aerosol characterization significantly since extinction coefficients can be measured independently from backscattering coefficients. In particular, HSRL can measure aerosol extinction during daytime and nighttime with a high sensitivity. We developed an HSRL with the iodine filter method for continuous observation of aerosols at 532nm in the northern region of Argentina in the framework of the South American Environmental Atmospheric Risk Management Network (SAVER.Net)/SATREPS project. The laser wavelength of the HSRL was controlled by a feedback system to tune the laser wavelength to the center of an iodine absorption line. The stability of the laser wavelength with the system satisfied the requirement showing very small systematic errors in the retrieval of extinction and backscatter.

  12. 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.

  13. Aerosol chemical elemental mass concentration at lower free troposphere

    Energy Technology Data Exchange (ETDEWEB)

    Carmo Freitas, Maria do [Reactor-ITN, Technological and Nuclear Institute, E.N. 10, 2686-953 Sacavem (Portugal)], E-mail: cfreitas@itn.pt; Dionisio, Isabel [Reactor-ITN, Technological and Nuclear Institute, E.N. 10, 2686-953 Sacavem (Portugal); Fialho, Paulo; Barata, Filipe [Chemistry and Physics of Atmosphere, Azores University, 9701-851 Terra Cha (Portugal)

    2007-08-21

    This paper shows the use of Instrumental neutron activation analysis (INAA) technique to determine elemental masses collected by a seven-wavelength Aethalometer instrument at the summit of Pico mountain in the Azorean archipelago, situated in the Central North Atlantic Ocean. Each sample corresponds to air particulate matter measured continuously for periods of approximately 24 h taken from 14th July 2001 through 14th July 2002. The statistical analysis of the coefficients of correlation between all the elements identified, permitted to establish six groups that could potentially be associated with the type of source responsible for the aerosol sampled in the lower free troposphere at the Azorean archipelago. Calculation of the synoptic back trajectories helped to corroborate the use of the iron/cesium relation as a tracer for the Saharan dust aerosol. It was demonstrated that INAA constituted an important tool to identify these events.

  14. Patterns in atmospheric carbonaceous aerosols in China: emission estimates and observed concentrations

    Directory of Open Access Journals (Sweden)

    H. Cui

    2015-03-01

    rural and remote sites, attributed partly to weaker atmospheric oxidation and SOC formation compared to summer. Enhanced SOC formation from oxidization and anthropogenic activities like biomass combustion is judged to have crucial effects on severe haze events characterized by high particle concentrations. Several observational studies indicate an increasing trend in ambient OC/EC (but not in OC or EC individually from 2000 to 2010, confirming increased atmospheric oxidation of OC across the country. Combining the results of emission estimation and observations, the improvement over prior emission inventories is indicated by inter-annual comparisons and correlation analysis. It is also indicated, however, that the estimated growth in emissions might be faster than observed growth, and that some sources with high primary OC/EC like burning of biomass are still underestimated. Further studies to determine changing emission factors over time in the residential sector and to compare to other measurements such as satellite observations are thus suggested to improve understanding of the levels and trends of primary carbonaceous aerosol emissions in China.

  15. Organosulfates and organic acids in Arctic aerosols: speciation, annual variation and concentration levels

    Directory of Open Access Journals (Sweden)

    A. M. K. Hansen

    2014-02-01

    Full Text Available Sources, composition and occurrence of secondary organic aerosols (SOA in the Arctic were investigated at Zeppelin Mountain, Svalbard, and Station Nord, northeast Greenland, during the full annual cycle of 2008 and 2010 respectively. We focused on the speciation of three types of SOA tracers: organic acids, organosulfates and nitrooxy organosulfates from both anthropogenic and biogenic precursors, here presenting organosulfate concentrations and compositions during a full annual cycle and chemical speciation of organosulfates in Arctic aerosols for the first time. Aerosol samples were analysed using High Performance Liquid Chromatography coupled to a quadrupole Time-of-Flight mass spectrometer (HPLC-q-TOF-MS. A total of 11 organic acids (terpenylic acid, benzoic acid, phthalic acid, pinic acid, suberic acid, azelaic acid, adipic acid, pimelic acid, pinonic acid, diaterpenylic acid acetate (DTAA and 3-methyl-1,2,3-butanetricarboxylic acid (MBTCA, 12 organosulfates and one nitrooxy organosulfate were identified at the two sites. Six out of the 12 organosulfates are reported for the first time. Concentrations of organosulfates follow a distinct annual pattern at Station Nord, where high concentration were observed in late winter and early spring, with a mean total concentration of 47 (±14 ng m−3, accounting for 7 (±2% of total organic matter, contrary to a considerably lower organosulfate mean concentration of 2 (±3 ng m−3 (accounting for 1 (±1% of total organic matter observed during the rest of the year. The organic acids followed the same temporal trend as the organosulfates at Station Nord; however the variations in organic acid concentrations were less pronounced, with a total mean organic acid concentration of 11.5 (±4 ng m−3 (accounting for 1.7 (±0.6% of total organic matter in late winter and early spring, and 2.2 (±1 ng m−3 (accounting for 0.9 (±0.4% of total organic matter during the rest of the year. At Zeppelin Mountain

  16. 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

  17. Worldwide impact of aerosol's time scale on the predicted long-term concentrating solar power potential.

    Science.gov (United States)

    Ruiz-Arias, Jose A; Gueymard, Christian A; Santos-Alamillos, Francisco J; Pozo-Vázquez, David

    2016-08-10

    Concentrating solar technologies, which are fuelled by the direct normal component of solar irradiance (DNI), are among the most promising solar technologies. Currently, the state-of the-art methods for DNI evaluation use datasets of aerosol optical depth (AOD) with only coarse (typically monthly) temporal resolution. Using daily AOD data from both site-specific observations at ground stations as well as gridded model estimates, a methodology is developed to evaluate how the calculated long-term DNI resource is affected by using AOD data averaged over periods from 1 to 30 days. It is demonstrated here that the use of monthly representations of AOD leads to systematic underestimations of the predicted long-term DNI up to 10% in some areas with high solar resource, which may result in detrimental consequences for the bankability of concentrating solar power projects. Recommendations for the use of either daily or monthly AOD data are provided on a geographical basis.

  18. Wintertime Arctic Ocean sea water properties and primary marine aerosol concentrations

    Directory of Open Access Journals (Sweden)

    J. Zábori

    2012-11-01

    Full Text Available Sea spray aerosols are an important part of the climate system through their direct and indirect effects. Due to the diminishing sea ice, the Arctic Ocean is one of the most rapidly changing sea spray aerosol source areas. However, the influence of these changes on primary particle production is not known.

    In laboratory experiments we examined the influence of Arctic Ocean water temperature, salinity, and oxygen saturation on primary particle concentration characteristics. Sea water temperature was identified as the most important of these parameters. A strong decrease in sea spray aerosol production with increasing water temperature was observed for water temperatures between −1°C and 9°C. Aerosol number concentrations decreased from at least 1400 cm−3 to 350 cm−3. In general, the aerosol number size distribution exhibited a robust shape with one mode close to dry diameter Dp 0.2 μm with approximately 45% of particles at smaller sizes. Changes in sea water temperature did not result in pronounced change of the shape of the aerosol size distribution, only in the magnitude of the concentrations. Our experiments indicate that changes in aerosol emissions are most likely linked to changes of the physical properties of sea water at low temperatures. The observed strong dependence of sea spray aerosol concentrations on sea water temperature, with a large fraction of the emitted particles in the typical cloud condensation nuclei size range, provide strong arguments for a more careful consideration of this effect in climate models.

  19. Wintertime Arctic Ocean sea water properties and primary marine aerosol concentrations

    Directory of Open Access Journals (Sweden)

    J. Zábori

    2012-06-01

    Full Text Available Sea spray aerosols are an important part of the climate system through their direct and indirect effects. Due to the diminishing sea ice, the Arctic Ocean is one of the most rapidly changing sea spray aerosol source areas. However, the influence of these changes on primary particle production is not known.

    In laboratory experiments we examined the influence of Arctic Ocean water temperature, salinity and oxygen saturation on primary particle concentration characteristics. Sea water temperature was identified as the most important of these parameters. A strong decrease in sea spray aerosol production with increasing water temperature was observed for water temperatures between −1 °C and 9 °C. Aerosol number concentrations decreased from at least 1400 cm−3 to 350 cm−3. In general, the aerosol number size distribution exhibited a robust shape with one mode close to Dp 0.2 μm with approximately 45% of particles at smaller sizes. Changes in sea water temperature did not result in pronounced change of the shape of the aerosol size distribution, only in the magnitude of the concentrations. Our experiments indicate that changes in aerosol emissions are most likely linked to changes of the physical properties of sea water at low temperatures. The observed strong dependence of sea spray aerosol concentrations on sea water temperature, with a large fraction of the emitted particles in the typical cloud condensation nuclei size range, provide strong arguments for a more careful consideration of this effect in climate models.

  20. Aircraft measurements of ozone, NOx, CO, and aerosol concentrations in biomass burning smoke over Indonesia and Australia in October 1997: Depleted ozone layer at low altitude over Indonesia

    Science.gov (United States)

    Tsutsumi, Yukitomo; Sawa, Yousuke; Makino, Yukio; Jensen, Jørgen B.; Gras, John L.; Ryan, Brian F.; Diharto, Sri; Harjanto, Hery

    The 1997 El Niño unfolded as one of the most sever El Niño Southern Oscillation (ENSO) events in this century and it coincided with massive biomass burning in the equatorial western Pacific region. To assess the influence on the atmosphere, aircraft observations of trace gases and aerosol were conducted over Kalimantan in Indonesia and Australia. Over Kalimantan in Indonesia, high concentrations of O3, NOx, CO, and aerosols were observed during the flight. Although the aerosol and NOx decreased with altitude, the O3 had the maximum concentration (80.5 ppbv) in the middle layer of the smoke haze and recorded very low concentrations (˜20 ppbv) in the lower smoke layer. This feature was not observed in the Australian smoke. We proposed several hypotheses for the low O3 concentration at low levels over Kalimantan. The most likely are lack of solar radiation and losses at the surface of aerosol particles.

  1. Aerosol Characteristics at a High Altitude Location in Central Himalayas: Optical Properties and Radiative Forcing

    CERN Document Server

    Pant, P; Dumka, U C; Sagar, R; Satheesh, S K; Moorthy, K K; Sagar, Ram

    2006-01-01

    Collocated measurements of the mass concentrations of aerosol black carbon (BC) and composite aerosols near the surface were carried out along with spectral aerosol optical depths (AODs) from a high altitude station, Manora Peak in Central Himalayas, during a comprehensive aerosol field campaign in December 2004. Despite being a pristine location in the Shivalik Ranges of Central Himalayas, and having a monthly mean AOD (at 500 nm) of 0.059 $\\pm$ 0.033 (typical to this site), total suspended particulate (TSP) concentration was in the range 15 - 40 micro g m^(-3) (mean value 27.1 $\\pm$ 8.3 micro g m^(-3)). Interestingly, aerosol BC had a mean concentration of 1.36 $\\pm$ 0.99 micro g m^(-3), contributed to ~5.0 $\\pm$ 1.3 % to the composite aerosol mass. This large abundance of BC is found to have linkages to the human activities in the adjoining valley and to the boundary layer dynamics. Consequently, the inferred single scattering albedo lies in the range of 0.87 to 0.94 (mean value 0.90 $\\pm$ 0.03), indicatin...

  2. [Concentration and Particle Size Distribution of Microbiological Aerosol During Haze Days in Beijing].

    Science.gov (United States)

    Hu, Ling-fei; Zhang, Ke; Wang, Hong-bao; Li, Na; Wang, Jie; Yang, Wen-hui; Yin, Zhe; Jiao, Zhou-guang; Wen, Zhan-bo; Li, Jin-song

    2015-09-01

    In this study, we evaluated the bacterial, fungal aerosol concentration, and particle size distribution using microbiological aerosol sampler, and analyzed the particles count concentration of PM1.0, PM2.5, PM5.0 and PM10.0 using aerodynamic particle sizer during clear and haze days in Beijing during Jan 8th, 2013 to Feb 4th, 2013. The concentration of bacterial, fungal aerosol, air particulate matter and aerosol distribution were compared between haze days and clear days. Our results indicated that the proportion of fungal particles smaller than 5 micron, which could deposit in lungs or deeper regions, was much higher than bacterial particles. The biological concentration of bacteria and fungi were higher in clear days than in haze days, and there was no statistic difference of the microbiological aerosol distribution. The concentration of air particulate matter were higher in haze days than in clear days, PM10 was the main particulate matters both in clear days and haze days.

  3. Dependence of SOA oxidation on organic aerosol mass concentration and OH exposure: experimental PAM chamber studies

    Directory of Open Access Journals (Sweden)

    E. Kang

    2011-02-01

    Full Text Available The oxidation of secondary organic aerosol (SOA is studied with mass spectra analysis of SOA formed in a Potential Aerosol Mass (PAM chamber, a small flow-through photo-oxidation chamber with extremely high OH and ozone levels. The OH exposure from a few minutes in the PAM chamber is similar to that from days to weeks in the atmosphere. The mass spectra were measured with a Quadrupole Aerosol Mass Spectrometer (Q-AMS for SOA formed from oxidation of α-pinene, m-xylene, p-xylene, and a mixture of the three. The organic mass fractions of m/z 44 (CO2+ and m/z 43 (mainly C2H3O+, named f44 and f43 respectively, are used as indicators of the degree of organic aerosol (OA oxidation that occurs as the OA mass concentration or the OH exposure are varied. The degree of oxidation is sensitive to both. For a fixed OH exposure, the degree of oxidation initially decreases rapidly and then more slowly as the OA mass concentration increases. For fixed initial precursor VOC amounts, the degree of oxidation increases linearly with OH exposure, with f44 increasing and f43 decreasing. In this study, the degree of SOA oxidation spans much of the range observed in the atmosphere. These results, while sensitive to the determination of f44 and f43, provide evidence that some characteristics of atmospheric OA oxidation can be generated in a PAM chamber. For all measurements in this study, the sum of f44 and f43 is 0.25 ± 0.03, so that the slope of a linear regression is approximately −1 on an f44 vs. f43 plot. This constancy of the sum suggests that these ions are complete proxies for organic mass in the OA studied.

  4. Size segregated aerosol mass concentration measurements over the Arabian Sea during ICARB

    Indian Academy of Sciences (India)

    Vijayakumar S Nair; K Krishna Moorthy; S Suresh Babu; K Narasimhulu; L Siva Sankara Reddy; R Ramakrishna Reddy; K Rama Gopal; V Sreekanth; B L Madhavan; K Niranjan

    2008-07-01

    Mass concentration and mass size distribution of total (composite) aerosols near the surface are essential inputs needed in developing aerosol models for radiative forcing estimation as well as to infer the environment and air quality. Using extensive measurements onboard the oceanographic research vessel, Sagar Kanya, during its cruise SK223B in the second phase of the ocean segment of the Integrated Campaign for Aerosols, gases and Radiation Budget (ICARB), the spatial distribution of the mass concentration and mass size distribution of near-surface aerosols are examined for the first time over the entire Arabian Sea, going as far as 58°E and 22°N, within a span of 26 days. In general, the mass concentrations () were found to be low with the mean value for the entire Arabian Sea being 16.7 ± 7 g m−3; almost 1/2 of the values reported in some of the earlier campaigns. Coarse mode aerosols contributed, on an average, 58% to the total mass, even though at a few pockets accumulation mode contribution dominated. Spatially, significant variations were observed over central and northern Arabian Sea as well as close to the west coast of India. In central Arabian Sea, even though the was quite low, contribution of accumulation aerosols to the total mass concentration was greater than 50%. Effective radius, a parameter important in determining scattering properties of aerosol size distribution, varied between 0.07 and 0.4 m with a mean value of 0.2 m. Number size distributions, deduced from the mass size distributions, were approximated to inverse power-law form and the size indices () were estimated. It was found to vary in the range 3.9 to 4.2 with a mean value of 4.0 for the entire oceanic region. Extinction coefficients, estimated using the number-size distributions, were well-correlated with the accumulation mode mass concentration with a correlation coefficient of 0.82.

  5. Ambient aerosol chlorine concentrations and artefacts during the MEGAPOLI Paris campaigns

    Science.gov (United States)

    Furger, Markus; Visser, Suzanne; Slowik, Jay; Crippa, Monica; Poulain, Laurent; Sciare, Jean; Flechsig, Uwe; Prévôt, André; Baltensperger, Urs

    2015-04-01

    Trace elements, especially those that are toxic, can affect the environment in significant ways. Studying them is advantageous with respect to a refinement of source apportionment when measured with high time resolution and appropriate size segregation. This approach is especially useful in urban environments with numerous time-variant emission sources distributed across a relatively narrow space. Two field campaigns took place in the framework of the MEGAPOLI project in Paris, France: one in the summer of 2009 (1-31 July), the other in the winter of 2010 (11 Jan - 10 Feb). Rotating drum impactors (RDI) were operated at an urban and a suburban site in each campaign. The RDI segregated the aerosols into three size ranges (PM10-2.5, PM2.5-1.0 and PM1.0-0.3) and sampled with 2-hour time resolution. The samples were analyzed with synchrotron radiation-induced X-ray fluorescence spectrometry (SR-XRF) at the synchrotron facility of the Paul Scherrer Institute (SLS), where a broad range of elements (Na, Mg, Al, Si, P, S, Cl, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn) was analyzed for each size range. Time series of the analyzed elements for the different sites and campaigns were prepared to characterize the aerosol trace element composition and temporal behavior for different weather situations and urban environments. Quality assurance was performed partly by intercomparison with independent measurements. An exceptional behavior was observed for chlorine (Cl), where periods with zero RDI concentration alternated with periods of normal load. Zero concentrations were not observed in particle-into-liquid (PILS) measurements. This identifies the observed behavior as a RDI sampling artefact. Nevertheless, the non-zero periods of Cl concentrations are still a gain in information compared to conventional sampling techniques, mainly due to the high time resolution.

  6. Atmospheric aerosol brown carbon in the high Himalayas

    Science.gov (United States)

    Kirillova, Elena; Decesari, Stefano; Marinoni, Angela; Bonasoni, Paolo; Vuillermoz, Elisa; Facchini, M. Cristina; Fuzzi, Sandro

    2016-04-01

    Anthropogenic light-absorbing atmospheric aerosol can reach very high concentrations in the planetary boundary layer in South-East Asia ("brown clouds"), affecting atmospheric transparency and generating spatial gradients of temperature over land with a possible impact on atmospheric dynamics and monsoon circulation. Besides black carbon (BC), an important light-absorbing component of anthropogenic aerosols is the organic carbon component known as 'brown carbon' (BrC). In this research, we provided first measurements of atmospheric aerosol BrC in the high Himalayas during different seasons. Aerosol sampling was conducted at the GAW-WMO Global station "Nepal Climate Observatory-Pyramid" (NCO-P) located in the high Khumbu valley at 5079 m a.s.l. in the foothills of Mt. Everest. PM10 aerosol samples were collected from July 2013 to November 2014. The sampling strategy was set up in order to discriminate the daytime valley breeze bringing polluted air masses up to the observatory and free tropospheric air during nighttime. Water-soluble BrC (WS-BrC) and methanol-soluble BrC (MeS-BrC) were extracted and analyzed using a UV/VIS spectrophotometer equipped with a 50 cm liquid waveguide capillary cell. In the polluted air masses, the highest levels of the BrC light absorption coefficient at 365 nm (babs365) were observed during the pre-monsoon season (1.83±1.46 Mm-1 for WS-BrC and 2.86±2.49 Mm-1 for MeS-BrC) and the lowest during the monsoon season (0.21±0.22 Mm-1 for WS-BrC and 0.32±0.29 Mm-1 for MeS-BrC). The pre-monsoon season is the most frequently influenced by a strong atmospheric brown cloud (ABC) transport to NCO-P due to increased convection and mixing layer height over South Asia combined with the highest up-valley wind speed and the increase of the emissions from open fires due to the agricultural practice along the Himalayas foothills and the Indo-Gangetic Plain. In contrast, the monsoon season is characterized by a weakened valley wind regime and an

  7. Biological aerosol particle concentrations and size distributions measured in pristine tropical rainforest air during AMAZE-08

    Science.gov (United States)

    Huffman, J. A.; Sinha, B.; Garland, R. M.; Snee-Pollmann, A.; Gunthe, S. S.; Artaxo, P.; Martin, S. T.; Andreae, M. O.; Pöschl, U.

    2012-09-01

    As a part of the AMAZE-08 campaign during the wet season in the rainforest of Central Amazonia, an ultraviolet aerodynamic particle sizer (UV-APS) was operated for continuous measurements of fluorescent biological aerosol particles (FBAP). In the coarse particle size range (> 1 μm) the campaign median and quartiles of FBAP number and mass concentration were 7.3 × 104 m-3 (4.0-13.2 × 104 m-3) and 0.72 μg m-3 (0.42-1.19 μg mm-3), respectively, accounting for 24% (11-41%) of total particle number and 47% (25-65%) of total particle mass. During the five-week campaign in February-March 2008 the concentration of coarse-mode Saharan dust particles was highly variable. In contrast, FBAP concentrations remained fairly constant over the course of weeks and had a consistent daily pattern, peaking several hours before sunrise, suggesting observed FBAP was dominated by nocturnal spore emission. This conclusion was supported by the consistent FBAP number size distribution peaking at 2.3 μm, also attributed to fungal spores and mixed biological particles by scanning electron microscopy (SEM), light microscopy and biochemical staining. A second primary biological aerosol particle (PBAP) mode between 0.5 and 1.0 μm was also observed by SEM, but exhibited little fluorescence and no fungal staining. This mode consisted of single bacterial cells, brochosomes and various fragments of biological material. Particles liquid-coated with mixed organic-inorganic material constituted a large fraction of observations, and these coatings contained salts likely from primary biological origin. We provide key support for the suggestion that real-time laser-induce fluorescence (LIF) techniques provide size-resolved concentrations of FBAP as a lower limit for the atmospheric abundance of biological particles. We also show that primary biological particles, fungal spores in particular, are key fractions of supermicron aerosol in the Amazon and that, especially when coated by mixed inorganic

  8. Biological aerosol particle concentrations and size distributions measured in pristine tropical rainforest air during AMAZE-08

    Directory of Open Access Journals (Sweden)

    J. A. Huffman

    2012-09-01

    Full Text Available As a part of the AMAZE-08 campaign during the wet season in the rainforest of Central Amazonia, an ultraviolet aerodynamic particle sizer (UV-APS was operated for continuous measurements of fluorescent biological aerosol particles (FBAP. In the coarse particle size range (> 1 μm the campaign median and quartiles of FBAP number and mass concentration were 7.3 × 104 m−3 (4.0–13.2 × 104 m−3 and 0.72 μg m−3 (0.42–1.19 μg mm−3, respectively, accounting for 24% (11–41% of total particle number and 47% (25–65% of total particle mass. During the five-week campaign in February–March 2008 the concentration of coarse-mode Saharan dust particles was highly variable. In contrast, FBAP concentrations remained fairly constant over the course of weeks and had a consistent daily pattern, peaking several hours before sunrise, suggesting observed FBAP was dominated by nocturnal spore emission. This conclusion was supported by the consistent FBAP number size distribution peaking at 2.3 μm, also attributed to fungal spores and mixed biological particles by scanning electron microscopy (SEM, light microscopy and biochemical staining. A second primary biological aerosol particle (PBAP mode between 0.5 and 1.0 μm was also observed by SEM, but exhibited little fluorescence and no fungal staining. This mode consisted of single bacterial cells, brochosomes and various fragments of biological material. Particles liquid-coated with mixed organic-inorganic material constituted a large fraction of observations, and these coatings contained salts likely from primary biological origin. We provide key support for the suggestion that real-time laser-induce fluorescence (LIF techniques provide size-resolved concentrations of FBAP as a lower limit for the atmospheric abundance of biological particles. We also show that primary biological particles, fungal spores in particular, are key

  9. The Influence of Aerosol Concentration on Changes in the Volumetric Activities of Indoor Radon Short-Term Decay Products

    Directory of Open Access Journals (Sweden)

    Diana Politova

    2011-02-01

    Full Text Available The article describes the influence of aerosol concentration on changes in the volumetric activities of indoor radon short-term decay products. The concentration of aerosol in the air, equilibrium factors and unattached fraction were measured under normal living conditions when the concentration of aerosol increases, i.e. burning a candle or frankincense in accommodations, smoke-filled accommodations, a steamy kitchen etc. It has been established that when the concentration of aerosol in the air rises, the number of free atoms of radon short-term decay products attached to aerosol particles also increases, and therefore higher volumetric activity of alpha particles is fixed. A tight positive connection of the correlation between equilibrium factor (F and aerosol particle concentration in the air of accommodations as well as a negative correlation between unattached fraction and an equilibrium factor have been determined.Article in Lithuanian

  10. Evaluation of a Low-Cost Aerosol Sensor to Assess Dust Concentrations in a Swine Building.

    Science.gov (United States)

    Jones, Samuel; Anthony, T Renée; Sousan, Sinan; Altmaier, Ralph; Park, Jae Hong; Peters, Thomas M

    2016-06-01

    Exposure to dust is a known occupational hazard in the swine industry, although efforts to measure exposures are labor intensive and costly. In this study, we evaluated a Dylos DC1100 as a low-cost (~$200) alternative to assess respirable dust concentrations in a swine building in winter. Dust concentrations were measured with collocated monitors (Dylos DC1100; an aerosol photometer, the pDR-1200; and a respirable sampler analyzed gravimetrically) placed in two locations within a swine farrowing building in winter for 18-24-h periods. The particle number concentrations measured with the DC1100 were converted to mass concentration using two methods: Physical Property Method and Regression Method. Raw number concentrations from the DC1100 were highly correlated to mass concentrations measured with the pDR-1200 with a coefficient of determination (R (2)) of 0.85, indicating that the two monitors respond similarly to respirable dust in this environment. Both methods of converting DC1100 number concentrations to mass concentrations yielded strong linear relationships relative to that measured with the pDR-1200 (Physical Property Method: slope = 1.03, R (2) = 0.72; Regression Method: slope = 0.72, R (2) = 0.73) and relative to that measured gravimetrically (Physical Property Method: slope = 1.08, R (2) = 0.64; Regression Method: slope = 0.75, R (2) = 0.62). The DC1100 can be used as a reasonable indicator of respirable mass concentrations within a CAFO and may have broader applicability to other agricultural and industrial settings. © The Author 2016. Published by Oxford University Press on behalf of the British Occupational Hygiene Society.

  11. Sensitivity of modelled sulfate aerosol and its radiative effect on climate to ocean DMS concentration and air-sea flux

    Science.gov (United States)

    Tesdal, Jan-Erik; Christian, James R.; Monahan, Adam H.; von Salzen, Knut

    2016-09-01

    Dimethylsulfide (DMS) is a well-known marine trace gas that is emitted from the ocean and subsequently oxidizes to sulfate in the atmosphere. Sulfate aerosols in the atmosphere have direct and indirect effects on the amount of solar radiation reaching the Earth's surface. Thus, as a potential source of sulfate, ocean efflux of DMS needs to be accounted for in climate studies. Seawater concentration of DMS is highly variable in space and time, which in turn leads to high spatial and temporal variability in ocean DMS emissions. Because of sparse sampling (in both space and time), large uncertainties remain regarding ocean DMS concentration. In this study, we use an atmospheric general circulation model with explicit aerosol chemistry (CanAM4.1) and several climatologies of surface ocean DMS concentration to assess uncertainties about the climate impact of ocean DMS efflux. Despite substantial variation in the spatial pattern and seasonal evolution of simulated DMS fluxes, the global-mean radiative effect of sulfate is approximately linearly proportional to the global-mean surface flux of DMS; the spatial and temporal distribution of ocean DMS efflux has only a minor effect on the global radiation budget. The effect of the spatial structure, however, generates statistically significant changes in the global-mean concentrations of some aerosol species. The effect of seasonality on the net radiative effect is larger than that of spatial distribution and is significant at global scale.

  12. [A simple testing installation for the production of aerosols with constant bacteria-contaminated concentrations].

    Science.gov (United States)

    Herbst, M; Lehmhus, H; Oldenburg, B; Orlowski, C; Ohgke, H

    1983-04-01

    A simple experimental set for the production and investigation of bacterially contaminated solid-state aerosols with constant concentration is described. The experimental set consists mainly of a fluidized bed-particle generator within a modified chamber for formaldehyde desinfection. The special conditions for the production of a defined concentration of particles and microorganisms are to be found out empirically. In a first application aerosol-sizing of an Andersen sampler is investigated. The findings of Andersen (1) are confirmed with respect to our experimental conditions.

  13. Role of aldehyde chemistry and NOx concentrations in secondary organic aerosol formation

    Directory of Open Access Journals (Sweden)

    P. O. Wennberg

    2010-08-01

    Full Text Available Aldehydes are an important class of products from atmospheric oxidation of hydrocarbons. Isoprene (2-methyl-1,3-butadiene, the most abundantly emitted atmospheric non-methane hydrocarbon, produces a significant amount of secondary organic aerosol (SOA via methacrolein (a C4-unsaturated aldehyde under urban high-NOx conditions. Previously, we have identified peroxy methacryloyl nitrate (MPAN as the important intermediate to isoprene and methacrolein SOA in this NOx regime. Here we show that as a result of this chemistry, NO2 enhances SOA formation from methacrolein and two other α, β-unsaturated aldehydes, specifically acrolein and crotonaldehyde, a NOx effect on SOA formation previously unrecognized. Oligoesters of dihydroxycarboxylic acids and hydroxynitrooxycarboxylic acids are observed to increase with increasing NO2/NO ratio, and previous characterizations are confirmed by both online and offline high-resolution mass spectrometry techniques. Molecular structure also determines the amount of SOA formation, as the SOA mass yields are the highest for aldehydes that are α, β-unsaturated and contain an additional methyl group on the α-carbon. Aerosol formation from 2-methyl-3-buten-2-ol (MBO232 is insignificant, even under high-NO2 conditions, as PAN (peroxy acyl nitrate, RC(OOONO2 formation is structurally unfavorable. At atmospherically relevant NO2/NO ratios (3–8, the SOA yields from isoprene high-NOx photooxidation are 3 times greater than previously measured at lower NO2/NO ratios. At sufficiently high NO2 concentrations, in systems of α, β-unsaturated aldehydes, SOA formation from subsequent oxidation of products from acyl peroxyl radicals+NO2 can exceed that from RO2+HO2 reactions under the same inorganic seed conditions, making RO2+NO2 an important channel for SOA formation.

  14. Role of aldehyde chemistry and NOx concentrations in secondary organic aerosol formation

    Directory of Open Access Journals (Sweden)

    P. O. Wennberg

    2010-04-01

    Full Text Available Aldehydes are an important class of products from atmospheric oxidation of hydrocarbons. Isoprene (2-methyl-1,3-butadiene, the most abundantly emitted atmospheric non-methane hydrocarbon, produces a significant amount of secondary organic aerosol (SOA via methacrolein (a C4-unsaturated aldehyde under urban high-NOx conditions. Previously, we have identified peroxy methacryloyl nitrate (MPAN as the important intermediate to isoprene and methacrolein SOA in this NOx regime. Here we show that as a result of this chemistry, NO2 enhances SOA formation from methacrolein and two other α, β-unsaturated aldehydes, specifically acrolein and crotonaldehyde, a NOx effect on SOA formation previously unrecognized. Oligoesters of dihydroxycarboxylic acids and hydroxynitrooxycarboxylic acids are observed to increase with increasing NO2/NO ratio, and previous characterizations are confirmed by both online and offline high-resolution mass spectrometry techniques. Molecular structure also determines the amount of SOA formation, as the SOA mass yields are the highest for aldehydes that are α, β-unsaturated and contain an additional methyl group on the α-carbon. Aerosol formation from 2-methyl-3-buten-2-ol (MBO232 is insignificant, even under high-NO2 conditions, as PAN (peroxy acyl nitrate, RC(OOONO2 formation is structurally unfavorable. At atmospherically relevant NO2/NO ratios, the SOA yields from isoprene high-NOxphotooxidation are 3 times greater than previously measured at lower NO2/NO ratios. At sufficiently high NO2 concentrations, in systems of α, β-unsaturated aldehydes, SOA formation from subsequent oxidation of products from acyl peroxyl radicals+NO2 can exceed that from RO2+HO2 reactions under the same inorganic seed conditions, making RO2+NO2 an important channel for SOA formation.

  15. Amazon boundary layer aerosol concentration sustained by vertical transport during rainfall

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Jian; Krejci, Radovan; Giangrande, Scott; Kuang, Chongai; Barbosa, Henrique M. J.; Brito, Joel; Carbone, Samara; Chi, Xuguang; Comstock, Jennifer; Ditas, Florian; Lavric, Jost; Manninen, Hanna E.; Mei, Fan; Moran-Zuloaga, Daniel; Pöhlker, Christopher; Pöhlker, Mira L.; Saturno, Jorge; Schmid, Beat; Souza, Rodrigo A. F.; Springston, Stephen R.; Tomlinson, Jason M.; Toto, Tami; Walter, David; Wimmer, Daniela; Smith, James N.; Kulmala, Markku; Machado, Luiz A. T.; Artaxo, Paulo; Andreae, Meinrat O.; Petäjä, Tuukka; Martin, Scot T.

    2016-10-24

    A necessary prerequisite of cloud formation, aerosol particles represent one of the largest uncertainties in computer simulations of climate change1,2, in part because of a poor understanding of processes under natural conditions3,4. The Amazon rainforest is one of the few continental regions where aerosol particles and their precursors can be studied under near-natural conditions5-7. Cloud condensation nuclei (CCN) in clean Amazonia are mostly produced by the growth of smaller particles in the boundary layer8-10, whereas these smaller particles themselves 31 appear to be produced elsewhere5,11. Key questions are in what part of the atmosphere they might 32 be produced and what could be the transport processes that deliver them to the boundary layer, where they grow into CCN. Here, using recent aircraft measurements above central Amazonia, we show high concentrations of small particles in the lower free troposphere. The particle size spectrum shifts towards larger sizes with decreasing altitude, implying particle growth as air descends from the free troposphere towards Earth's surface. Complementary measurements at ground sites show that free tropospheric air having high concentrations of small particles (diameters of less than 50 nm) is transported into the boundary layer during precipitation events, both by strong convective downdrafts and by weaker downward motions in the trailing stratiform region. This vertical transport helps maintain the population of small particles and ultimately CCN in the boundary layer, thereby playing an important role in controlling the climate state under natural conditions. In contrast, this mechanism becomes masked under polluted conditions, which sometimes prevail at times in Amazonia as well as over other tropical continental regions5,12.

  16. Spatial variability of aerosol and black carbon concentrations in the troposphere of the Russian Arctic

    Science.gov (United States)

    Kozlov, Valerii S.; Panchenko, Mikhail V.; Paris, Jean D.; Nédéléc, Philippe; Chernov, Dmitry G.; Shmargunov, Vladimir P.

    2015-11-01

    A cycle of flights of the Optik TU-134 Flying Laboratory of IAO SB RAS over regions of Western Siberia and the Russian Arctic (55.0-74.8°N, 61.3-82.9°E) was carried out on October 15-17 of 2014 within the framework of the YAK-AEROSIB Russian—French Project. The mass concentrations of submicron aerosol and Black Carbon (BC) in the troposphere up to a height of 8.5 km were measured in the flights. The ranges of variability were 0.3-20 μg/m3 for the aerosol concentration and 0.02-1 μg/m3 for the BC concentration. In the subpolar latitudes of 71-74.8°N, the lower levels of aerosol (0.8-6 μg/m3) and BC (0.02-0.3 μg/m3) were observed. The comparison of the results of airborne sensing in 2008 and 2014 has shown that in the Western Subartic the aerosol and BC concentrations in the vertical profiles up to six times exceeded those observed in the Eastern Subarctic (0.3-1 μg/m3 and 10-50 ng/m3). The excess of the mean integral BC concentrations and the aerosol optical depth was, on average, 2-2.5 times (0.16 mg/m2; 0.02). In the region of the Kara Sea at heights of 0.5-2 and 4-6 km, the excess of the aerosol content in the western sector in comparison with the eastern one was, on average, 2 times, while for the black carbon the excess achieved 7 times at heights of 1-2 km (0.25- 0.035 μg/m3). The mean integral concentrations of aerosol and black carbon ˜ 1.3 times exceeded those in the clearer eastern region of the sea (0.31 mg/m2; 0.049). The obtained estimates indicate the decrease of the aerosol and BC concentrations in the subpolar latitudes of the Russian Federation from the west to the east.

  17. Simultaneous retrieval of aerosol optical thickness and chlorophyll concentration from multi-wavelength measurement over East China Sea

    Science.gov (United States)

    Shi, C.; Nakajima, T.; Hashimoto, M.

    2016-12-01

    A flexible inversion algorithm is proposed for simultaneously retrieving aerosol optical thickness (AOT) and surface chlorophyll a (Chl) concentration from multi-wavelength observation over the ocean. In this algorithm, forward radiation calculation is performed by an accurate coupled atmosphere-ocean model with a sophisticated bio-optical ocean module, which is different from those in the classic ocean color algorithms that decouple the atmosphere and ocean systems using atmospheric correction procedures. Then, a full-physical nonlinear optimization approximation approach is used to retrieve AOT and Chl. For AOT retrieval, a global three-dimensional spectral radiation-transport aerosol model is used as the priori constraint to increase the retrieval accuracy of aerosol. To investigate the algorithm's availability, the retrieval experiment is conducted using simulated radiance data to demonstrate that the relative errors in simultaneously determining AOT and Chl can be mostly controlled to within 10% using multi-wavelength and angle coving in and out of sunglint. Furthermore, the inversion results are assessed using the actual satellite observation data obtained from Greenhouse gas Observation SATellite (GOSAT) and MODerate resolution Imaging Spectroradiometer (MODIS)/Aqua instruments through comparison to Aerosol Robotic Network (AERONET) aerosol and ocean color (OC) products over East China Sea. Both the retrieved AOT and Chl compare favorably to the reported AERONET values, particularly when using the CASE 2 ocean module in turbid water, even when the retrieval is performed in the presence of high aerosol loading and sun glint. Finally, the MODIS images are used to jointly retrieve the spatial distribution of AOT and Chl in comparison to the MODIS AOT and OC products.

  18. Dielectric Spectra of Aerosol OT/Water Systems at Different Concentrations and Temperatures

    Institute of Scientific and Technical Information of China (English)

    ZHAO Kong-shuang; JIA Zhan-jie; YANG Li-kun; XIAO Jin-xin

    2011-01-01

    The dielectric spectra of aerosol OT[AOT,sodium(bis-2-ethylhexyl)sulfosuccinate]/water systems at different concentrations and temperatures were investigated by the dielectric relaxation spectroscopy(DRS).Through the dielectric spectra of different concentrations,two dielectric relaxations were observed over a frequency range from 40 Hz to 110 MHz and the mechanisms of the relaxations were also interpreted based on the Grosse's model.The low-frequency relaxation(around 105 Hz)was attributed to the radial diffusion of counterions along the long-half axis of the rod-like micelle,and the high-frequency relaxation(around 106 Hz)was ascribed to the radial diffusion of counterions along the short-half axis.Furthermore,specific emphasis was placed on studying the effects of temperature on system's conductivity.It was observed that the low-frequency limit of conductivity(k1)decreased and then increased with the increment of temperature under the measured concentration.On the other hand,the conductivity(km and kh)in meso-and high-frequency ranges always increased as temperature increased.Both the tendencies of alteration which mentioned above should be related to the phase transition of AOT/water system.

  19. Evolution of planetary boundary layer under different weather conditions, and its impact on aerosol concentrations

    Institute of Scientific and Technical Information of China (English)

    Jiannong Quan; Yang Gao; Qiang Zhang; Xuexi Tie; Junji Cao; Suqin Han; Junwang Meng

    2013-01-01

    A field experiment was conducted in Tianjin,China from September 9-30,2010,focused on the evolution of Planetary Boundary Layer (PBL) and its impact on surface air pollutants.The experiment used three remote sensing instruments,wind profile radar (WPR),microwave radiometer (MWR) and micro-pulse lidar (MPL),to detect the vertical profiles of winds,temperature,and aerosol backscattering coefficient and to measure the vertical profiles of surface pollutants (aerosol,CO,SO2,NOx),and also collected sonic anemometers data from a 255-m meteorological tower.Based on these measurements,the evolution of the PBL was estimated.The averaged PBL height was about 1000-1300 m during noon/afternoon-time,and 200-300 m during night-time.The PBL height and the aerosol concentrations were anti-correlated during clear and haze conditions.The averaged maximum PBL heights were 1.08 and 1.70 km while the averaged aerosol concentrations were 52 and 17 μg/m3 under haze and clear sky conditions,respectively.The influence of aerosols and clouds on solar radiation was observed based on sonic anemometers data collected from the 255-m meteorological tower.The heat flux was found significantly decreased by haze (heavy pollution) or cloud,which tended to depress the development of PBL,while the repressed structure of PBL further weakened the diffusion of pollutants,leading to heavy pollution.This possible positive feedback cycle (more aerosols → lower PBL height → more aerosols) would induce an acceleration process for heavy ground pollution in megacities.

  20. Production Mechanism, Number Concentration, Size Distribution, Chemical Composition, and Optical Properties of Sea Spray Aerosols Workshop, Summer 2012

    Energy Technology Data Exchange (ETDEWEB)

    Meskhidze, Nicholas [NCSU

    2013-10-21

    The objective of this workshop was to address the most urgent open science questions for improved quantification of sea spray aerosol-radiation-climate interactions. Sea spray emission and its influence on global climate remains one of the most uncertain components of the aerosol-radiation-climate problem, but has received less attention than other aerosol processes (e.g. production of terrestrial secondary organic aerosols). Thus, the special emphasis was placed on the production flux of sea spray aerosol particles, their number concentration and chemical composition and properties.

  1. Mass Concentration and Mineralogical Characteristics Aerosol Particles Collected at Dunhuang During ACE-Asia

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    Measurements were performed in spring 2001 and 2002 to determine the characteristics of soil dust in the Chinese desert region of Dunhuang, one of the ground sites of the Asia-Pacific Regional Aerosol Characterization Experiment (ACE-Asia). The mean mass concentrations of total suspended particle matter during the spring of 2001 and 2002 were 317 μg m-3 and 307 μg m-3, respectively. Eleven dust storm events were observed with a mean aerosol concentration of 1095 μg m-3, while the non-dusty days with calm or weak wind speed had a background aerosol loading of 196 μg m-3 on average in the springtime.The main minerals detected in the aerosol samples by X-ray diffraction were illite, kaolinite, chlorite, quartz,feldspar, calcite and dolomite. Gypsum, halite and amphibole were also detected in a few samples. The mineralogical data also show that Asian dust is characterized by a kaolinite to chlorite (K/C) ratio lower than 1 whereas Saharan dust exhibits a K/C ratio larger than 2. Air mass back-trajectory analysis show that three families of pathways are associated with the aerosol particle transport to Dunhuang, but these have similar K/C ratios, which further demonstrates that the mineralogical characteristics of Asian dust are different from African dust.

  2. Size-segregated concentration of heavy metals in an urban aerosol of the Balkans region (Belgrade

    Directory of Open Access Journals (Sweden)

    Đorđević D.

    2013-04-01

    Full Text Available This work focuses on the heavy metals contents of the size-segregated urban aerosol of the continental area of Balkans. The distribution of nano/micron heavy metals in the size-segregated urban aerosol of Belgrade center was studied during the summer–autumn of 2008. The particle size distribution in the size ranges Dp ≤ 0.49 μm, 0.49 ≤ Dp ≤ 0.95 μm, 0.95 ≤ Dp ≤ 1.5 μm, 1.5 ≤ Dp ≤ 3.0 μm, 3.0 ≤ Dp ≤ 7.2 μm and Dp ≥ 7.2 μm was measured. The aerosol samples were submitted to gravimetric and chemical analyses. The obtained mean mass concentration of the PM fractions was in accordance with an urban aerosol distribution. The aerosol mass concentrations were determined by gravimetric measurements (mGM and, for heavy metals analyzed by ICP/MS.

  3. Aerosol Characteristics at a high-altitude station Nainital during the ISRO-GBP Land Campaign-II

    CERN Document Server

    Saha, A; Dumka, U C; Hegde, P; Srivastava, M K; Sagar, R; Saha, Auromeet; Srivastava, Manoj K.; Sagar, Ram

    2006-01-01

    During the second land campaign (LC-II) organised by ISRO-GBP, extensive ground-based measurements of aerosol characteristics were carried out over Manora Peak (29.4oN; 79.5oE; 1951 metres above mean sea level), Nainital (a high altitude station located in the Shivalik ranges of Central Himalayas) during the dry, winter season (December) of 2004. These measurements included the spectral aerosol optical depths (AOD), columnar water vapour content (W), Total Columnar Ozone (TCO), total number concentration (NT) of near surface aerosols, mass concentration of black carbon (MB), aerosol mass loading (MT), and Global Solar Radiation. Based on these measured parameters, we present the results on the near-surface and columnar properties of atmospheric aerosols at Nainital.

  4. Tire-tread and bitumen particle concentrations in aerosol and soil samples

    DEFF Research Database (Denmark)

    Fauser, Patrik; Tjell, Jens Christian; Mosbæk, Hans;

    2002-01-01

    ire and bitumen particle concentrations are determined in aerosol and soil samples. They each constitute about 5 wt-% of the total suspended particulate matter (TSP) in inner city air, collected with a Berner low pressure impactor, 5 m from a road. The particle size distribution shows that 92% of...

  5. Ambient Aerosol in Southeast Asia: High Resolution Aerosol Mass Spectrometer Measurements Over Oil Palm (Elaeis guineensis)

    Science.gov (United States)

    Phillips, G.; Dimarco, C.; Misztal, P.; Nemitz, E.; Farmer, D.; Kimmel, J.; Jimenez, J.

    2008-12-01

    The emission of organic compounds in the troposphere is important factor in the formation of secondary organic aerosol (SOA). A very large proportion of organic material emitted globally is estimated to arise from biogenic sources, with almost half coming from tropical and sub-tropical forests. Preliminary analyses of leave cuvette emission studies suggest that oil palm (Elaeis guineensis) is a significantly larger source of isoprene than tropical forest. Much larger sources of isoprene over oil palm allied with a larger anthropogenic component of local emissions contrast greatly with the remote tropical forest environment and therefore the character of SOA formed may differ significantly. These issues, allied with the high price of palm oil on international markets leading to increased use of land for oil palm production, could give rise to rapidly changing chemical and aerosol regimes in the tropics. It is therefore important to understand the current emissions and composition of organic aerosol over all important land-uses in the tropical environment. This in turn will lead to a greater understanding of the present, and to an improvement in predictive capacity for the future system. To help address these issues, a high resolution time of flight aerosol mass spectrometer (HR-ToF-AMS) was deployed in the Sabahmas (PPB OIL) oil palm plantation near Lahad Datu, in Eastern Sabah, as part of the field component of the Aerosol Coupling in the Earth System (ACES) project, part of the UK NERC APPRAISE program. This project was allied closely with measurements made of similar chemical species and aerosol components at a forest site in the Danum Valley as part of the UK Oxidant and Particle Photochemical Processes above a Southeast Asian tropical rainforest (OP3) project. Measurements of submicron non- refractory aerosol composition are presented along with some preliminary analysis of chemically resolved aerosol fluxes made with a new eddy covariance system, based on the

  6. Activity Concentration Monitoring for Alpha Radioactive Aerosol in CRARL after Reprocessing Experiments

    Institute of Scientific and Technical Information of China (English)

    WANG; Xiang-li; LIU; Ning; WANG; Xiao-rong; BAI; Yang; JIAO; Xiao-yan; XU; Xin; MA; Hao-ran

    2015-01-01

    The activity concentration for alpha radioactive aerosol in CRARL after reprocessing experiments was analyzed.Through the decay method of activity concentration monitoring,the processed result shows the background is 3.05×10-3 s-1,σ(0)=2.25×10-3,LC=2.33×10-3 Bq/m3,LD=4.66×10-3 Bq/m3.The result indicated

  7. Fast Airborne Aerosol Size and Chemistry Measurements with the High Resolution Aerosol Mass Spectrometer during the MILAGRO Campaign

    Science.gov (United States)

    DeCarlo, P. F.; Dunlea, E. J.; Kimmel, J. R.; Aiken, A. C.; Sueper, D.; Crounse, J.; Wennberg, P. O.; Emmons, L.; Shinozuka, Y.; Clarke, A.; Zhou, J.; Tomlinson, J.; Collins,D. R.; Knapp, D.; Weinheimer, A. J.; Montzka,D. D.; Campos,T.; Jimenez, J. L.

    2007-01-01

    The concentration, size, and composition of non-refractory submicron aerosol (NR-PM(sub l)) was measured over Mexico City and central Mexico with a High-Resolution Time-of-Flight Aerosol Mass Spectrometer (HR-ToF-AMS) onboard the NSF/NCAR C-130 aircraft as part of the MILAGRO field campaign. This was the first aircraft deployment of the HR-ToF-AMS. During the campaign the instrument performed very well, and provided 12 s data. The aerosol mass from the AMS correlates strongly with other aerosol measurements on board the aircraft. Organic aerosol (OA) species dominate the NR-PM(sub l) mass. OA correlates strongly with CO and HCN indicating that pollution (mostly secondary OA, SOA) and biomass burning (BB) are the main OA sources. The OA to CO ratio indicates a typical value for aged air of around 80 microg/cubic m (STP) ppm(exp -1). This is within the range observed in outflow from the Northeastern US, which could be due to a compensating effect between higher BB but lower biogenic VOC emissions during this study. The O/C atomic ratio for OA is calculated from the HR mass spectra and shows a clear increase with photochemical age, as SOA forms rapidly and quickly overwhelms primary urban OA, consistent with Volkamer et al. (2006) and Kleinman et al. (2008). The stability of the OA/CO while O/C increases with photochemical age implies a net loss of carbon from the OA. BB OA is marked by signals at m/z 60 and 73, and also by a signal enhancement at large m/z indicative of larger molecules or more resistance to fragmentation. The main inorganic components show different spatial patterns and size distributions. Sulfate is regional in nature with clear volcanic and petrochemical/power plant sources, while the urban area is not a major regional source for this species. Nitrate is enhanced significantly in the urban area and immediate outflow, and is strongly correlated with CO indicating a strong urban source. The importance of nitrate decreases with distance from the city

  8. Fast airborne aerosol size and chemistry measurements with the high resolution aerosol mass spectrometer during the MILAGRO Campaign

    Science.gov (United States)

    Decarlo, P. F.; Dunlea, E. J.; Kimmel, J. R.; Aiken, A. C.; Sueper, D.; Crounse, J.; Wennberg, P. O.; Emmons, L.; Shinozuka, Y.; Clarke, A.; Zhou, J.; Tomlinson, J.; Collins, D. R.; Knapp, D.; Weinheimer, A. J.; Montzka, D. D.; Campos, T.; Jimenez, J. L.

    2007-12-01

    The concentration, size, and composition of non-refractory submicron aerosol (NR-PM1) was measured over Mexico City and central Mexico with a High-Resolution Time-of-Flight Aerosol Mass Spectrometer (HR-ToF-AMS) onboard the NSF/NCAR C-130 aircraft as part of the MILAGRO field campaign. This was the first aircraft deployment of the HR-ToF-AMS, in which the instrument performed very well, and provided 12 s data. The aerosol mass from the AMS correlates strongly with other aerosol measurements on board the aircraft. Organic aerosol (OA) species dominate the NR-PM1 mass. OA correlates strongly with CO and HCN indicating that pollution (mostly secondary OA, SOA) and biomass burning (BB) are the main OA sources. The OA to CO ratio indicates a typical value for aged air of around 80 μg m-3 (STP) ppm-1. This is within the range observed in outflow from the Northeastern US, which could be due to a compensating effect between higher BB but lower biogenic VOC emissions during this study. The O/C atomic ratio for OA is calculated from the HR mass spectra and shows a clear increase with photochemical age, as SOA forms rapidly and quickly overwhelms primary urban OA, consistent with Volkamer et al. (2006) and Kleinman et al. (2007b). BB OA is marked by signals at m/z 60 and 73, and also by a signal enhancement at large m/z indicative of larger molecules or more resistance to fragmentation. The main inorganic components show different spatial patterns and size distributions. Sulfate is regional in nature with clear volcanic and petrochemical/power plant sources, while the urban area is not a major source for this species. Nitrate is enhanced significantly in the urban area and immediate outflow, and is strongly correlated with CO indicating a strong urban source. The importance of nitrate decreases with distance from the city likely due to evaporation. BB does not appear to be a strong source of nitrate despite its high emissions of nitrogen oxides, presumably due to low ammonia

  9. Fast airborne aerosol size and chemistry measurements with the high resolution aerosol mass spectrometer during the MILAGRO Campaign

    Directory of Open Access Journals (Sweden)

    P. F. DeCarlo

    2007-12-01

    Full Text Available The concentration, size, and composition of non-refractory submicron aerosol (NR-PM1 was measured over Mexico City and central Mexico with a High-Resolution Time-of-Flight Aerosol Mass Spectrometer (HR-ToF-AMS onboard the NSF/NCAR C-130 aircraft as part of the MILAGRO field campaign. This was the first aircraft deployment of the HR-ToF-AMS, in which the instrument performed very well, and provided 12 s data. The aerosol mass from the AMS correlates strongly with other aerosol measurements on board the aircraft. Organic aerosol (OA species dominate the NR-PM1 mass. OA correlates strongly with CO and HCN indicating that pollution (mostly secondary OA, SOA and biomass burning (BB are the main OA sources. The OA to CO ratio indicates a typical value for aged air of around 80 μg m−3 (STP ppm−1. This is within the range observed in outflow from the Northeastern US, which could be due to a compensating effect between higher BB but lower biogenic VOC emissions during this study. The O/C atomic ratio for OA is calculated from the HR mass spectra and shows a clear increase with photochemical age, as SOA forms rapidly and quickly overwhelms primary urban OA, consistent with Volkamer et al. (2006 and Kleinman et al. (2007b. BB OA is marked by signals at m/z 60 and 73, and also by a signal enhancement at large m/z indicative of larger molecules or more resistance to fragmentation. The main inorganic components show different spatial patterns and size distributions. Sulfate is regional in nature with clear volcanic and petrochemical/power plant sources, while the urban area is not a major source for this species. Nitrate is enhanced significantly in the urban area and immediate outflow, and is strongly correlated with CO indicating a strong urban source. The importance of nitrate decreases with distance from the city likely due to evaporation. BB does not appear to be a strong source of nitrate

  10. On the potential contribution of open lead particle emissions to the central Arctic aerosol concentration

    Directory of Open Access Journals (Sweden)

    A. Held

    2010-10-01

    Full Text Available During the ice-breaker borne ASCOS expedition (Arctic Summer Cloud Ocean Study direct eddy covariance measurements of aerosol number fluxes were carried out in August 2008 on the edge of an ice floe drifting in the central Arctic Ocean between 2°–10° W longitude and 87°–87.5° N latitude. The median aerosol transfer velocities over different surface types (open water leads, ice ridges, snow and ice surfaces ranged from 0.27 to 0.68 mm s−1 during deposition-dominated episodes. Emission periods were observed more frequently over the open lead, while the snow behaved primarily as a deposition surface. Directly measured aerosol fluxes were compared with particle deposition parameterizations in order to estimate the emission flux from the observed net aerosol flux. Finally, the contribution of the open lead particle source to atmospheric variations in particle number concentration was evaluated and compared with the observed temporal evolution of particle number. The direct emission of aerosol particles from the open lead can only explain 5–10% of the observed particle number variation in the mixing layer close to the surface.

  11. Changes in concentration and size distribution of aerosols during fog over the south Indian Ocean

    Indian Academy of Sciences (India)

    Vimlesh Pant; C G Deshpande; A K Kamra

    2010-08-01

    Measurements of the concentration and size distribution of aerosol particles in the size-ranges of 0.5–20 m and 16–700 nm diameters were made during six fog episodes over the south Indian Ocean. Observations show that concentrations of particles of all sizes start decreasing 1–2 hours before the occurrence of fog. This decrease is more prominent for coarse particles of < 1 m diameter and continues until 10–20 minutes before the onset of fog when particle concentrations in all size ranges rapidly increase by one/two orders of magnitude in ∼20 minutes. Thereafter, concentrations of particles of all sizes gradually decrease until the dissipation of fog. After the fog dissipation, concentrations of coarse mode particles rapidly increase and restore to their pre-fog levels but concentrations of the Aitken mode particles decrease slowly and reach their pre-fog levels only after 1–2 hours. The net effect of fog is to change the bimodal size distributions of aerosols with a coarse mode at 1.0 m and an accumulation mode at 40–60 nm to a power law size distribution. It is proposed that the preferential growth and sedimentation of the coarse mode hygroscopic particles in the initial phase cause a large decrease in the aerosol surface area. As a result, the low vapour pressure gases which were initially being used for the growth of coarse mode particles, now accelerate the growth rates of the accumulation and Aitken mode particles.

  12. Aerosol production by high-velocity molten-metal droplets

    Energy Technology Data Exchange (ETDEWEB)

    Rader, D J; Benson, D A

    1988-06-01

    This report presents the results of an experimental study of the aerosol produced by high-velocity molten-metal droplets. These tests are intended to simulate the reduction of high-velocity fragments into aerosol in high-explosive detonations or reactor accidents involving nuclear materials. The primary droplets are produced by the heating and electromagnetic launch of metal wires; velocities approaching Mach 1 can be obtained at present. Size distributions obtained tungsten and zirconium droplets burning in air. Lognormal size distributions were observed in both cases with DMPS-equivalent mean diameters of about 0.4 ..mu..m and geometric standard deviations of about two. SEM and TEM analysis of aerosol samples collected by a point-to-plane electrostatic precipitator showed that the majority of these particles were web-like chain agglomerates. Tests performed in argon atmospheres produced several orders-of-magnitude less aerosol mass than in equivalent air tests, supporting the key role combustion plays in secondary aerosol generation. 26 refs., 14 figs., 2 tabs.

  13. Effect of aerosols and NO2 concentration on ultraviolet actinic flux near Mexico City during MILAGRO: measurements and model calculations

    Energy Technology Data Exchange (ETDEWEB)

    Palancar, G. G.; Lefer, B. L.; Hall, S. R.; Shaw, W. J.; Corr, C. A.; Herndon, S. C.; Slusser, J. R.; Madronich, S.

    2013-01-24

    Ultraviolet (UV) actinic fluxes (AF) measured with three Scanning Actinic Flux Spectroradiometers (SAFS) are compared with the Tropospheric Ultraviolet-Visible (TUV) model v.5 in order to assess the effects of aerosols and NO2 concentrations on the radiation. Measurements were made during the MILAGRO campaign near Mexico City in March 2006, at a ground-based station near Mexico City (the T1 supersite) and from the NSF/NCAR C-130 aircraft. At the surface, measurements are typically smaller by up to 25 % in the morning, 10% at noon, and 40% in the afternoon, than actinic flux modeled for clean, cloud-free conditions. When measurements of PBL height, NO2 concentration and aerosols optical properties are included in the model, the agreement improves to within ±10% in the morning and afternoon, and ±3% at noon. Based on daily averages, aerosols account for 68%, NO2 for 25%, and residual uncertainties for 7% of these AF reductions observed at the surface. Several overpasses from the C-130 aircraft provided the opportunity to examine the actinic flux perturbations aloft, and also show better agreement with the model when aerosol and NO2 effects are included above and below the flight altitude. TUV model simulations show that the vertical structure of the actinic flux is sensitive to the choice of the aerosol single scattering albedo (SSA) at UV wavelengths. Typically, aerosols caused enhanced AF above the PBL and reduced AF near the surface. However, for highly scattering aerosols (SSA > 0.95), enhancements can penetrate well into the PBL, while for strongly absorbing aerosols (SSA<0.7) reductions in AF are computed in the free troposphere as well as in the PBL. Finally, additional measurements of the SSA at these wavelengths are needed to better constrain the effect of aerosols on the vertical structure of the actinic flux.

  14. Vertical distribution of aerosol number concentration in the troposphere over Siberia derived from airborne in-situ measurements

    Science.gov (United States)

    Arshinov, Mikhail Yu.; Belan, Boris D.; Paris, Jean-Daniel; Machida, Toshinobu; Kozlov, Alexandr; Malyskin, Sergei; Simonenkov, Denis; Davydov, Denis; Fofonov, Alexandr

    2016-04-01

    Knowledge of the vertical distribution of aerosols particles is very important when estimating aerosol radiative effects. To date there are a lot of research programs aimed to study aerosol vertical distribution, but only a few ones exist in such insufficiently explored region as Siberia. Monthly research flights and several extensive airborne campaigns carried out in recent years in Siberian troposphere allowed the vertical distribution of aerosol number concentration to be summarized. In-situ aerosol measurements were performed in a wide range of particle sizes by means of improved version of the Novosibirsk-type diffusional particle sizer and GRIMM aerosol spectrometer Model 1.109. The data on aerosol vertical distribution enabled input parameters for the empirical equation of Jaenicke (1993) to be derived for Siberian troposphere up to 7 km. Vertical distributions of aerosol number concentration in different size ranges averaged for the main seasons of the year will be presented. This work was supported by Interdisciplinary integration projects of the Siberian Branch of the Russian Academy of Science No. 35, No. 70 and No. 131; the Branch of Geology, Geophysics and Mining Sciences of RAS (Program No. 5); and Russian Foundation for Basic Research (grant No. 14-05-00526). Jaenicke R. Tropospheric aerosols, in Aerosol-Cloud-Climate Interactions, edited by P.V. Hobs. -Academic Press, San Diego, CA, 1993.- P. 1-31.

  15. Significant increase of aerosol number concentrations in air masses crossing a densely trafficked sea area

    Directory of Open Access Journals (Sweden)

    Simonas Kecorius

    2016-01-01

    Full Text Available In this study, we evaluated 10 months data (September 2009 to June 2010 of atmospheric aerosol particle number size distribution at three atmospheric observation stations along the Baltic Sea coast: Vavihill (upwind, Sweden, Utö (upwind, Finland, and Preila (downwind, Lithuania. Differences in aerosol particle number size distributions between the upwind and downwind stations during situations of connected atmospheric flow, when the air passed each station, were used to assess the contribution of ship emissions to the aerosol number concentration (diameter interval 50–400 nm in the Lithuanian background coastal environment. A clear increase in particle number concentration could be noticed, by a factor of 1.9 from Utö to Preila (the average total number concentration at Utö was 791 cm−3, and by a factor of 1.6 from Vavihill to Preila (the average total number concentration at Vavihill was 998 cm−3. The simultaneous measurements of absorption Ångström exponents close to unity at Preila supported our conclusion that ship emissions in the Baltic Sea contributed to the increase in particle number concentration at Preila.

  16. FORMULATION OF AEROSOL CONCENTRATES CONTAINING HARUAN (Channa striatus FOR WOUND DRESSING

    Directory of Open Access Journals (Sweden)

    FEBRIYENTI

    2008-01-01

    Full Text Available The objective of this research was to formulate an aerosol concentrate containing haruan (Channa striatus water extract that would produce a thin film when sprayed onto a wound and could be used for wound dressing. The aerosol concentrates were formulated with various polymer and plasticiser mixtures and tested in dispersion systems. The polymers evaluated were hydroxypropyl methylcellulose (HPMC, carboxymethylcellulose sodium (CMC Sodium, acacia, tragacanth, chitosan, gelatine and gelatine (bloom 151–160, all at concentrations of 2%. The plasticisers evaluated were polyethylene glycol (PEG 400 and 4000, glycerine, propylene glycol, and triacetin. Films were prepared from film-forming dispersions by casting techniques. Film-forming dispersions were characterised in terms of pH, density, surface tension, rheological properties, particle size distribution, and tackiness. Based on these evaluations, HPMC was chosen as the best polymer. It produced a film with the expected qualities and was easy to reproduce in the form of dispersions or as thin transparent films. Glycerine was judged as the most appropriate plasticiser because it produced the concentrate having the desired qualities and properties expected from an aerosol concentrate

  17. Simulated impacts of direct radiative effects of scattering and absorbing aerosols on surface layer aerosol concentrations in China during a heavily polluted event in February 2014

    Science.gov (United States)

    Qiu, Yulu; Liao, Hong; Zhang, Renjian; Hu, Jianlin

    2017-06-01

    We quantified aerosol direct radiative effects on surface layer concentrations of aerosols during a heavily polluted event in the North China Plain (NCP, 35.4°N-41.2°N, 113.3°E-119.3°E) during 21-27 February 2014, using the chemistry version of the Weather Research and Forecasting (WRF-Chem) Model. Comparisons of model results with observations showed that the WRF-Chem model reproduced the spatial and temporal variations of meteorological variables reasonably well, but overestimated average PM2.5 concentration by 21.7% over the NCP during 21-27 February. The simulated direct radiative effects of total, absorbing, and scattering aerosols reduced the planetary boundary layer (PBL) heights by 111.4 m, 35.7 m, and 70.7 m, respectively, averaged over NCP and 21-27 February. The direct radiative effects of total aerosols induced increases in aerosol concentrations by 11.5% for SO42-, 29.5% for NO3-, 29.6% for NH4+, 28.7% for organic carbon (OC), 26.7% for black carbon (BC), and 20.4% for PM2.5, respectively, averaged over the NCP during 21-27 February 2014. The increase in PM2.5 concentration averaged over the NCP and the haze event was 29.6 μg m-3 (16.8%) due to radiative effect of scattering aerosols, as a result of the decreases in PBL height and changes in secondary aerosol production rates. The corresponding increase in PM2.5 concentration owing to absorbing aerosols was 2.1 μg m-3 (1.0%), resulting from the offsetting impacts of changes in PBL height, wind near the surface, and chemical processes.

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

    Science.gov (United States)

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

    2016-04-01

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

  19. Aerosol mass and black carbon concentrations, two year-round observations at NCO-P (5079 m, Southern Himalayas

    Directory of Open Access Journals (Sweden)

    A. Marinoni

    2010-03-01

    Full Text Available Aerosol mass and the absorbing fraction are important variables, needed to constrain the role of atmospheric particles in the Earth radiation budget, both directly and indirectly through CCN activation. In particular, their monitoring in remote areas and mountain sites is essential for determining source regions, elucidating the mechanisms of long range transport of anthropogenic pollutants, and validating regional and global models. Since March 2006, aerosol mass and black carbon concentration have been monitored at the Nepal Climate Observatory-Pyramid, a permanent high-altitude research station located in the Khumbu valley at 5079 m a.s.l. below Mt. Everest. The first two-year averages of PM1 and PM1-10 mass were 1.94 μg m−3 and 1.88 μg m−3, with standard deviations of 3.90 μg m−3 and 4.45 μg m−3, respectively, while the black carbon concentration average is 160.5 ng m−3, with a standard deviation of 296.1 ng m−3. Both aerosol mass and black carbon show well defined annual cycles, with a maximum during the pre-monsoon season and a minimum during the monsoon. They also display a typical diurnal cycle during all the seasons, with the lowest particle concentration recorded during the night, and a considerable increase during the afternoon, revealing the major role played by thermal winds in influencing the behaviour of atmospheric compounds over the high Himalayas. The aerosol concentration is subject to high variability: in fact, as well as frequent "background conditions" (55% of the time when BC concentrations are mainly below 100 ng m−3, concentrations up to 5 μg m−3 are reached during some episodes (a few days every year in the pre-monsoon seasons. The variability of PM and BC is the result of both short-term changes due to thermal wind development in the valley, and long-range transport/synoptic circulation. At

  20. Aerosol mass and black carbon concentrations, a two year record at NCO-P (5079 m, Southern Himalayas

    Directory of Open Access Journals (Sweden)

    A. Marinoni

    2010-09-01

    Full Text Available Aerosol mass and the absorbing fraction are important variables, needed to constrain the role of atmospheric particles in the Earth radiation budget, both directly and indirectly through CCN activation. In particular, their monitoring in remote areas and mountain sites is essential for determining source regions, elucidating the mechanisms of long range transport of anthropogenic pollutants, and validating regional and global models. Since March 2006, aerosol mass and black carbon concentration have been monitored at the Nepal Climate Observatory-Pyramid, a permanent high-altitude research station located in the Khumbu valley at 5079 m a.s.l. below Mt. Everest. The first two-year averages of PM1 and PM1−10 mass were 1.94 μg m−3 and 1.88 μg m−3, with standard deviations of 3.90 μg m−3 and 4.45 μg m−3, respectively, while the black carbon concentration average is 160.5 ng m−3, with a standard deviation of 296.1 ng m−3. Both aerosol mass and black carbon show well defined annual cycles, with a maximum during the pre-monsoon season and a minimum during the monsoon. They also display a typical diurnal cycle during all the seasons, with the lowest particle concentration recorded during the night, and a considerable increase during the afternoon, revealing the major role played by thermal winds in influencing the behaviour of atmospheric compounds over the high Himalayas. The aerosol concentration is subject to high variability: in fact, as well as frequent "background conditions" (55% of the time when BC concentrations are mainly below 100 ng m−3, concentrations up to 5 μg m−3 are reached during some episodes (a few days every year in the pre-monsoon seasons. The variability of PM and BC is the result of both short-term changes due to thermal wind development in the valley, and long-range transport/synoptic circulation

  1. Aerosols for Concentrating Solar Electricity Production Forecasts: Requirement Quantification and ECMWF/MACC Aerosol Forecast Assessment

    OpenAIRE

    Schroedter-Homscheidt, Marion; Oumbe, Armel; Benedetti, Angela; Morcrette, Jean-Jacques

    2013-01-01

    The potential for transferring a larger share of our energy supply toward renewable energy is a widely discussed goal in society, economics, environment, and climate-related programs. For a larger share of electricity to come from fluctuating solar and wind energy-based electricity, production forecasts are required to ensure successful grid integration. Concentrating solar power holds the potential to make the fluctuating solar electricity a dispatchable resource by using both heat storage s...

  2. Chemical composition of free tropospheric aerosol for PM1 and coarse mode at the high alpine site Jungfraujoch

    Directory of Open Access Journals (Sweden)

    J. Cozic

    2008-01-01

    Full Text Available The chemical composition of submicron (fine mode and supermicron (coarse mode aerosol particles has been investigated at the Jungfraujoch high alpine research station (3580 m a.s.l., Switzerland as part of the GAW aerosol monitoring program since 1999. A clear seasonality was observed for all major components throughout the period with low concentrations in winter (predominantly free tropospheric aerosol and higher concentrations in summer (enhanced vertical transport of boundary layer pollutants. In addition, mass closure was attempted during intensive campaigns in March 2004, February–March 2005 and August 2005. Ionic, carbonaceous and non-refractory components of the aerosol were quantified as well as the PM1 and coarse mode total aerosol mass concentrations. A relatively low conversion factor of 1.8 for organic carbon (OC to particulate organic matter (OM was found in winter (February–March 2005. Organics, sulfate, ammonium, and nitrate were the major components of the fine aerosol fraction that were identified, while calcium and nitrate were the only two measured components contributing to the coarse mode. The aerosol mass concentrations for fine and coarse mode aerosol measured during the intensive campaigns were not typical of the long-term seasonality due largely to dynamical differences. Average fine and coarse mode concentrations during the intensive field campaigns were 1.7 μg m−3 and 2.4 μg m−3 in winter and 2.5 μg m−3 and 2.0 μg m−3 in summer, respectively. The mass balance of aerosols showed higher contributions of calcium and nitrate in the coarse mode during Saharan dust events (SDE than without SDE.

  3. Chemical composition of free tropospheric aerosol for PM1 and coarse mode at the high alpine site Jungfraujoch

    Directory of Open Access Journals (Sweden)

    J. Cozic

    2007-08-01

    Full Text Available The chemical composition of submicron (fine mode and supermicron (coarse mode aerosol particles has been investigated since 1999 within the GAW aerosol monitoring program at the high alpine research station Jungfraujoch (3580 m a.s.l., Switzerland. Clear seasonality was observed for all major components in the last 9 years with low concentrations in winter (predominantly free tropospheric aerosol and higher concentrations in summer (enhanced vertical transport of boundary layer pollutants. In addition, mass closure was attempted during intensive experiments in March 2004, February–March 2005 and August 2005. Ionic, carbonaceous and refractory components of the aerosol were quantified as well as the PM1 and coarse mode total aerosol mass concentrations. A relatively low conversion factor of 1.8 for organic carbon (OC to particulate organic matter (OM in winter (February–March 2005 was found. Organics, sulfate, ammonium, and nitrate were the major identified components of the fine aerosol fraction, while calcium and nitrate were the two major measured components in the coarse mode. The aerosol mass concentrations for fine and coarse mode aerosol during the intensive campaigns were not typical of the long term seasonality due largely to dynamical differences. Average fine and coarse mode concentrations during the intensive field campaigns were 1.7 μg m−3 and 2.4 μg m−3 in winter and 2.5 μg m−3 and 2.0 μg m−3 in summer, respectively. The mass balance of aerosols showed higher contributions of calcium and nitrate in the coarse mode during Saharan dust events (SDE than without SDE.

  4. Observations of fluorescent aerosol-cloud interactions in the free troposphere at the Sphinx high Alpine research station, Jungfraujoch

    Science.gov (United States)

    Crawford, I.; Lloyd, G.; Bower, K. N.; Connolly, P. J.; Flynn, M. J.; Kaye, P. H.; Choularton, T. W.; Gallagher, M. W.

    2015-09-01

    The fluorescent nature of aerosol at a high Alpine site was studied using a wide-band integrated bioaerosol (WIBS-4) single particle multi-channel ultra violet-light induced fluorescence (UV-LIF) spectrometer. This was supported by comprehensive cloud microphysics and meteorological measurements with the aims of cataloguing concentrations of bio-fluorescent aerosols at this high altitude site and also investigating possible influences of UV-fluorescent particle types on cloud-aerosol processes. Analysis of background free tropospheric air masses, using a total aerosol inlet, showed there to be a minor but statistically insignificant increase in the fluorescent aerosol fraction during in-cloud cases compared to out of cloud cases. The size dependence of the fluorescent aerosol fraction showed the larger aerosol to be more likely to be fluorescent with 80 % of 10 μm particles being fluorescent. Whilst the fluorescent particles were in the minority (NFl/NAll = 0.27±0.19), a new hierarchical agglomerative cluster analysis approach, Crawford et al. (2015) revealed the majority of the fluorescent aerosol were likely to be representative of fluorescent mineral dust. A minor episodic contribution from a cluster likely to be representative of primary biological aerosol particles (PBAP) was also observed with a wintertime baseline concentration of 0.1±0.4 L-1. Given the low concentration of this cluster and the typically low ice active fraction of studied PBAP (e.g. pseudomonas syringae) we suggest that the contribution to the observed ice crystal concentration at this location is not significant during the wintertime.

  5. 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.

  6. Compressed gas domestic aerosol valve design using high viscous product

    Directory of Open Access Journals (Sweden)

    A Nourian

    2016-10-01

    Full Text Available Most of the current universal consumer aerosol products using high viscous product such as cooking oil, antiperspirants, hair removal cream are primarily used LPG (Liquefied Petroleum Gas propellant which is unfriendly environmental. The advantages of the new innovative technology described in this paper are: i. No butane or other liquefied hydrocarbon gas is used as a propellant and it replaced with Compressed air, nitrogen or other safe gas propellant. ii. Customer acceptable spray quality and consistency during can lifetime iii. Conventional cans and filling technology There is only a feasible energy source which is inert gas (i.e. compressed air to replace VOCs (Volatile Organic Compounds and greenhouse gases, which must be avoided, to improve atomisation by generating gas bubbles and turbulence inside the atomiser insert and the actuator. This research concentrates on using "bubbly flow" in the valve stem, with injection of compressed gas into the passing flow, thus also generating turbulence. The new valve designed in this investigation using inert gases has advantageous over conventional valve with butane propellant using high viscous product (> 400 Cp because, when the valving arrangement is fully open, there are negligible energy losses as fluid passes through the valve from the interior of the container to the actuator insert. The use of valving arrangement thus permits all pressure drops to be controlled, resulting in improved control of atomising efficiency and flow rate, whereas in conventional valves a significant pressure drops occurs through the valve which has a complex effect on the corresponding spray.

  7. Aerosol composition and sources during high and low pollution periods in Ningbo, China

    Science.gov (United States)

    Xu, Jing-Sha; Xu, Hong-Hui; Xiao, Hang; Tong, Lei; Snape, Colin E.; Wang, Cheng-Jun; He, Jun

    2016-09-01

    Due to the rapid industrialization of the Yangtze River Delta (YRD) region in China, heavy air pollution episodes have occurred frequently over the past five years which are of great concern due to their environmental and health impacts. To investigate the chemical characteristics of the highly polluted aerosols in this region, a sampling campaign had been conducted in Ningbo from 3 December 2012 to 27 June 2013, during which a month long high pollution episode had been captured. Daily average PM2.5 concentrations during high and low pollution periods were 111 μg m-3 and 53 μg m-3, respectively. The most polluted day was 8 January 2013 with a PM2.5 concentration up to 175 μg m- 3. To understand the origin of the highly polluted aerosols, meteorological conditions, air mass backward trajectories, distribution of fire spots in surrounding areas and various categories of aerosol pollutants were analyzed, including trace metals, inorganic species, PAHs and anhydrosugars. Total metal concentrations were 3.8 and 1.6 μg m-3 for the high and low pollution episodes, respectively, accounting for 3.4% and 3.1% of the total PM2.5 mass. Total concentrations of ionic species accounted for more than 50.0% of the PM2.5 by mass, with dominant ions (nitrate, sulfate, ammonium) accounting for over 42.0% of the PM2.5 mass concentrations in both periods. During the high pollution episode, enhanced Cd-Pb and biomarker (levoglucosan, mannosan) levels indicated the contributions from coal combustion, traffic and biomass burning to fine aerosol PM2.5. The average diagnostic ratio of Fla/(Fla + Pyr) was 0.54 in high pollution episode, which was intermediate between that for wood (> 0.50) and coal combustion (0.58). BaP/Bpe was 0.49 and 0.30 for the highly and lightly polluted aerosols respectively, associated with the significant non-traffic emissions (pollution period and long-range transport of air masses from heavy industries and biomass burning from northern China to Ningbo could be

  8. Lidar observations of high-altitude aerosol layers (cirrus clouds)

    Science.gov (United States)

    Deleva, Atanaska D.; Grigorov, Ivan V.

    2013-03-01

    Aerosols, clouds and aerosol-cloud interactions are recognized as the key factors influencing the climate. Clouds are the primary modulators of the Earth's radiative budget. This paper focuses on the detection of high-altitude aerosol layers in the troposphere over mid-latitude lidar station in Sofia, Bulgaria. They are situated in the height-region 6 km÷16 km, with thickness in the range 0.2 km÷5 km and have varying optical characteristics. On the basis of the general utilized classification of the Cirrus clouds, high values of the calculated atmospheric backscatter coefficient and Angströmexponent estimation results we conclude that the registered strongly scattered aerosol layers are Cirrus clouds. Lidar measurements are performed with an aerosol lidar, equipped with Nd:YAG laser at wavelengths 532 nm and 1064 nm. Mainly, lidar data are presented in terms of vertical atmospheric backscatter coefficient profiles. We also include 2Dcolormap in height-time coordinates build on the basis of so called range corrected signals. It shows in general changes of the aerosol stratification over the lidar station during the measurement period. We employed HYSPLIT backward trajectories and DREAM forecasts to analyze the lidar profile outlines and characterize the events during which Cirrus cloud samples were observed. So was remarked that most of the results were obtained during Saharan dust long-way transport over the city of Sofia. Reported experimental examples are extracted from regular lidar investigations of the atmosphere within the frame of European project EARLINET.

  9. Contribution of carbonaceous material to cloud condensation nuclei concentrations in European background (Mt. Sonnblick) and urban (Vienna) aerosols

    Science.gov (United States)

    Hitzenberger, R.; Berner, A.; Giebl, H.; Kromp, R.; Larson, S. M.; Rouc, A.; Koch, A.; Marischka, S.; Puxbaum, H.

    During four intensive measurement campaigns (two on Mt. Sonnblick, European background aerosol, and two in Vienna, urban aerosol), cloud condensation nuclei (CCN) were measured at supersaturations of 0.5%. Impactor measurements of the mass size distribution in the size range 0.1-10 μm were performed and later analyzed for Cl -, NO -3, SO 2-4, Na +, NH +4, K +, Ca 2+ and Mg 2+ by ion chromatography, for total carbon (TC) using a combustion method, and for black carbon (BC) by an optical method (integrating sphere). Organic carbon (OC) was defined as the difference between TC (minus carbonate carbon) and BC. At all sites, the mass fraction of BC in the submicron aerosol was comparable (4-5%). CCN concentrations on Mt. Sonnblick were found to be 10-30% of those measured in Vienna, although high Mt. Sonnblick concentrations were comparable to low Vienna concentrations (around 800 cm -3). The contribution of organic material was estimated from the mass concentrations of the chemical species sampled on the impactor stage with the lowest cut point (0.1-0.215 μm aerodynamic equivalent diameter). On Mt. Sonnblick, TC material contributed 11% to the total mass in fall 1995, and 67% in summer 1996, while the OC fraction was 6 and 61%. The combined electrolytes and mineral material contributed 18 and 16% in fall and summer. During the Vienna spring campaign, the contributions of OC and electrolytes to the total mass concentration in this size range were 48 and 36%, respectively.

  10. [Characteristics of carbonaceous aerosol concentration in snow and ice of glaciers in Tianshan Mountains].

    Science.gov (United States)

    Wang, Sheng-Jie; Zhang, Ming-Jun; Wang, Fei-Teng; Li, Zhong-Qin

    2012-03-01

    The snow and ice samples, collected at Glacier No. 1 at the headwaters of Urumqi River (UG1) and Glacier No. 51 at Haxilegen of Kuytun River (HG51) in 2002 and 2004, were analyzed for organic carbon (OC) and element carbon (EC) by thermal/ optical reflectance (TOR). The spatio-temporal characteristics and environmental significance of OC and EC concentration were discussed in details. The concentration order of total carbon (TC) was: snowpack of west branch on UG1 (1 943 ng x g(-1)) > snowpack of east branch on UG1 (989 ng x g(-1)) > snowpack of HG51 (150 ng x g(-1)) > glacier ice of east branch on UG1 (77 ng x g(-1)), and the concentration order of OC and EC lay similar as TC. The concentration of OC and EC in snowpack of Tianshan Mountains were 557 ng x g(-1) and 188 ng x g(-1), respectively. Concentration peak of carbonaceous aerosol usually appeared near the dust layer at the bottom section of snowpack, but the some sudden events could increase the concentration in the surface snow. Because of the seasonality of carbon emission (e. g. heating and agricultural activities) and transportation (e. g. atmospheric circulation), the concentration of carbonaceous aerosol increased from July to November with fluctuations. Difference on the order of magnitude might exist between the concentration in snow (firn) and glacier ice, which was influenced by the glacier surroundings, sampling situation and other factors. EC on the surface snow affected the albedo significantly, and an average albedo reduction of 0.22 in the wavelength of 300-700 nm was simulated by SNICAR (snow, ice, and aerosol radiative) model.

  11. Aerosol particles at a high-altitude site on the Southeast Tibetan Plateau, China: Implications for pollution transport from South Asia

    Science.gov (United States)

    Zhao, Zhuzi; Cao, Junji; Shen, Zhenxing; Xu, Baiqing; Zhu, Chongshu; Chen, L.-W. Antony; Su, Xiaoli; Liu, Suixin; Han, Yongming; Wang, Gehui; Ho, Kinfai

    2013-10-01

    aerosol samples were collected from 16 July 2008 to 26 July 2009 at Lulang, a high-altitude (>3300m above sea level) site on the southeast Tibetan Plateau (TP); objectives were to determine chemical characteristics of the aerosol and identify its major sources. We report aerosol (total suspended particulate, TSP) mass levels and the concentrations of selected elements, carbonaceous species, and water-soluble inorganic ions. Significant buildup of aerosol mass and chemical species (organic carbon, element carbon, nitrate, and sulfate) occurred during the premonsoon, while lower concentrations were observed during the monsoon. Seasonal variations in aerosol and chemical species were driven by precipitation scavenging and atmospheric circulation. Two kinds of high-aerosol episodes were observed: one was enriched with dust indicators (Fe and Ca2+), and the other was enhanced with organic and elemental carbon (OC and EC), SO42-, NO3-, and Fe. The TSP loadings during the latter were 3 to 6 times those on normal days. The greatest aerosol optical depths (National Centers for Environmental Protection/National Center for Atmospheric Research reanalysis) occurred upwind, in eastern India and Bangladesh, and trajectory analysis indicates that air pollutants were transported from the southwest. Northwesterly winds brought high levels of natural emissions (Fe, Ca2+) and low levels of pollutants (SO42-, NO3-, K+, and EC); this was consistent with high aerosol optical depths over the western deserts and Gobi. Our work provides evidence that both geological and pollution aerosols from surrounding regions impact the aerosol population of the TP.

  12. On the aerosol-cloud relationship at a high-alpine site

    Energy Technology Data Exchange (ETDEWEB)

    Baltensperger, U.; Schwikowski, M.; Jost, D.T.; Nyeki, S.; Gaeggeler, H.W. [Paul Scherrer Inst. (PSI), Villigen (Switzerland)

    1997-09-01

    Field experiments at the Jungfraujoch showed that during the presence of a cloud, most of the aerosol mass is transferred into the cloud phase. This results in smaller cloud droplets for increasing aerosol concentration, which increases the albedo of clouds (known as the indirect effect of climate forcing by aerosol particles). (author) 1 fig., 4 refs.

  13. Concentrations and composition of aerosols and particulate matter in surface waters along the transatlantic section

    Science.gov (United States)

    Nemirovskaya, I. A.; Lisitzin, A. P.; Novigatsky, A. N.; Redzhepova, Z. U.; Dara, O. M.

    2016-07-01

    Along the transatlantic section from Ushuaia to Gdańsk (March 26-May 7, 2015; cruise 47 of R/V Akademik Ioffe), data were obtained on the concentrations of aerosols in the near-water layer of the atmosphere and of particulate matter in surface waters, as well as of organic compounds within the considered matter (Corg, chlorophyll a, lipids, and hydrocarbons). The concentrations of aerosols amounted to 1237-111 739 particles/L for the fraction of 0.3-1 μm and to 0.02-34.4 μg/m2/day for the matter collected by means of the network procedure. The distribution of aerosols is affected by circumcontinental zoning and by the fluxes from arid areas of African deserts. The maximum concentration of the treated compounds were found in the river-sea frontal area (the runoff of the Colorado River, Argentina), as well as when nearing the coasts, especially in the English Channel.

  14. Future Projections of Aerosol Optical Depth, Radiative Forcing, and Climate Response Due to Declining Aerosol Emissions in the Representative Concentration Pathways

    Science.gov (United States)

    Westervelt, D. M.; Mauzerall, D. L.; Horowitz, L. W.; Naik, V.

    2014-12-01

    It is widely expected that global emissions of atmospheric aerosols and their precursors will decrease strongly throughout the remainder of the 21st century, due to emission reduction policies enacted based on human health concerns. However, the resulting decrease in atmospheric aerosol burden will have unintended climate consequences. Since aerosols generally exert a net cooling influence on the climate, their removal will lead to an unmasking of global warming as well as other changes to the climate system. Aerosol and precursor global emissions decrease by as much as 80% by the year 2100, according to projections in four Representative Concentration Pathway (RCP) scenarios. We use the Geophysical Fluid Dynamics Laboratory Climate Model version 3 (GFDL CM3) to simulate future climate over the 21st century with and without aerosol emission changes projected by the RCPs in order to isolate the radiative forcing and climate response due to the aerosol reductions. We find that up to 1 W m-2 of radiative forcing may be unmasked globally by 2100 due to reductions in aerosol and precursor emissions, leading to average global temperature increases up to 1 K and global precipitation rate increases up to 0.09 mm d-1 (3%). Regionally and locally, climate impacts are much larger, as RCP8.5 projects a 2.1 K warming over China, Japan, and Korea due to reduced aerosol emissions. Our results highlight the importance of crafting emissions control policies with both climate and air pollution benefits in mind. The expected unmasking of additional global warming from aerosol reductions highlights the importance of robust greenhouse gas mitigation policies and may require more aggressive policies than anticipated.

  15. Chemical composition, sources, and processes of urban aerosols during summertime in Northwest China: insights from High Resolution Aerosol Mass Spectrometry

    Science.gov (United States)

    Xu, J.; Zhang, Q.; Chen, M.; Ge, X.; Ren, J.; Qin, D.

    2014-06-01

    An aerodyne High Resolution Time-of-Flight Aerosol Mass Spectrometer (HR-ToF-AMS) was deployed along with a Scanning Mobility Particle Sizer (SMPS) and a Multi Angle Absorption Photometers (MAAP) to measure the temporal variations of the mass loading, chemical composition, and size distribution of sub-micrometer particulate matter (PM1) in Lanzhou, northwest China, during 12 July-7 August 2012. The average PM1 mass concentration including non-refractory PM1 (NR-PM1) measured by HR-ToF-AMS and black carbon (BC) measured by MAAP during this study was 24.5 μg m-3 (ranging from 0.86 to 105μg m-3), with a mean composition consisting of 47% organics, 16% sulfate, 12% BC, 11% ammonium, 10% nitrate, and 4% chloride. The organics was consisted of 70% carbon, 21% oxygen, 8% hydrogen, and 1% nitrogen, with the average oxygen-to-carbon ratio (O / C) of 0.33 and organic mass-to-carbon ratio (OM / OC) of 1.58. Positive matrix factorization (PMF) of the high-resolution mass spectra of organic aerosols (OA) identified four distinct factors which represent, respectively, two primary OA (POA) emission sources (traffic and food cooking) and two secondary OA (SOA) types - a fresher, semi-volatile oxygenated OA (SV-OOA) and a more aged, low-volatility oxygenated OA (LV-OOA). Traffic-related hydrocarbon-like OA (HOA) and BC displayed distinct diurnal patterns both with peak at ~07:00-11:00 (BJT: UTC +8) corresponding to the morning rush hours, while cooking OA (COA) peaked during three meal periods. The diurnal profiles of sulfate and LV-OOA displayed a broad peak between ∼07:00-15:00, while those of nitrate, ammonium, and SV-OOA showed a narrower peak at ~08:00-13:00. The later morning and early afternoon peak in the diurnal profiles of secondary aerosol species was likely caused by mixing down of pollutants aloft, which were likely produced in the residual layer decoupled from the boundary layer during night time. The mass spectrum of SV-OOA also showed similarity with that of

  16. Effectiveness of leaded petrol phase-out in Tianjin, China based on the aerosol lead concentration and isotope abundance ratio

    Energy Technology Data Exchange (ETDEWEB)

    Wang Wan [Chinese Research Academy of Environmental Sciences, Beijing 100012 (China); Liu Xiande [Chinese Research Academy of Environmental Sciences, Beijing 100012 (China)]. E-mail: liuxdlxd@hotmail.com; Zhao Liwei [Tianjin Environmental Monitoring Center, Tianjin, 300190 (China); Guo, Dongfa [Beijing Research Institute of Uranium Geology, Beijing 100029 (China); Tian Xiaodan [University of Antwerp, UA, B-2610 Wilrijk-Antwerpen (Belgium); Adams, Freddy [University of Antwerp, UA, B-2610 Wilrijk-Antwerpen (Belgium)

    2006-07-01

    The phase-out of leaded petrol has been a measure widely used to reduce atmospheric lead pollution. Since the 1980s, China began to promote unleaded petrol. In order to assess the effectiveness of the measure an isotope fingerprint technique was applied for aerosol samples in the city of Tianjin. After dilute acid leaching, the lead concentration and isotope abundance ratios were determined for 123 samples collected in Tianjin during eight years (1994-2001). The {sup 206}Pb / {sup 207}Pb ratio was lower in summer, when coal combustion emission was low and vehicle exhaust became more important, indicating that the {sup 206}Pb / {sup 207}Pb ratio of leaded petrol in Tianjin is lower than that of aerosol samples. The {sup 206}Pb / {sup 207}Pb ratio gradually increased from 1994 to 2001, a trend that suggests that the contribution from vehicle exhaust was diminishing. Overall, the measurements matched well with national statistical data of leaded and unleaded petrol production. After the nationwide switch to unleaded gasoline, comprehensive control measures are urgently needed to reduce air lead pollution in China, as aerosol lead reduced slightly but remains at a relatively high level.

  17. Effectiveness of leaded petrol phase-out in Tianjin, China based on the aerosol lead concentration and isotope abundance ratio

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Wan; Liu, Xiande [Chinese Research Academy of Environmental Sciences, Beijing 100012 (China); Zhao, Liwei [Tianjin Environmental Monitoring Center, Tianjin, 300190 (China); Guo, Dongfa [Beijing Research Institute of Uranium Geology, Beijing 100029 (China); Tian, Xiaodan; Adams, Freddy [University of Antwerp, UA, B-2610 Wilrijk-Antwerpen (Belgium)

    2006-07-01

    The phase-out of leaded petrol has been a measure widely used to reduce atmospheric lead pollution. Since the 1980s, China began to promote unleaded petrol. In order to assess the effectiveness of the measure an isotope fingerprint technique was applied for aerosol samples in the city of Tianjin. After dilute acid leaching, the lead concentration and isotope abundance ratios were determined for 123 samples collected in Tianjin during eight years (1994-2001). The {sup 206}Pb/{sup 207}Pb ratio was lower in summer, when coal combustion emission was low and vehicle exhaust became more important, indicating that the {sup 206}Pb/{sup 207}Pb ratio of leaded petrol in Tianjin is lower than that of aerosol samples. The {sup 206}Pb/{sup 207}Pb ratio gradually increased from 1994 to 2001, a trend that suggests that the contribution from vehicle exhaust was diminishing. Overall, the measurements matched well with national statistical data of leaded and unleaded petrol production. After the nationwide switch to unleaded gasoline, comprehensive control measures are urgently needed to reduce air lead pollution in China, as aerosol lead reduced slightly but remains at a relatively high level. (author)

  18. Characteristics of black carbon aerosol mass concentration over the East Baltic region from two-year measurements.

    Science.gov (United States)

    Byčenkienė, Steigvilė; Ulevicius, Vidmantas; Kecorius, Simonas

    2011-04-01

    Continuous measurements of black carbon (BC) aerosol mass concentration were performed at a background site Preila (55°55'N, 21°00'E, 5 m a.s.l., Lithuania) during the period 2008-2009. The data were used to characterize the BC mass concentration distribution over the East Baltic region. High increase in aerosol BC concentration was associated with the change in air mass characteristics and biomass burning during the winter heating season and spring wildfires. Monthly means of BC concentration ranged from 212 to 1268 ng m(-3) and the highest hourly means of concentration were from 4800 to 6300 ng m(-3), predominantly in spring and winter months. During the October-April period the BC mass concentrations were about twice as high as those in the summertime. The BC diurnal pattern in winter was typically different from that in spring indicating the seasonal variation of the atmospheric boundary layer height. The weekday/weekend difference was not strongly pronounced because the BC concentrations in Preila are mainly affected by long-range transport or local sources. Typical periodicities caused by anthropogenic and meteorological influences have been identified using Fourier analysis. It was shown that domestic heating appears as a 365 day periodicity; traffic slightly contributes 5-7 day peaks in the spectrum and elevated long-range BC can be identified as characteristic peaks with periodicities in the range from 16 to 29 days.Temporal evolution and transport of BC aerosols were interpreted by the air mass backward trajectory analysis in conjunction with the examination of the wavelength dependence on the aethalometer data. Air masses originated from the North Atlantic Ocean and Scandinavia were favourable for lower BC concentrations (350 ng m(-3)), while the BC level associated with the Western Europe airflows was significantly higher (970 ng m(-3)). The mean values of Ångström exponent of the absorption coefficient (monthly means 1.45 ± 0.25 and 0.84 ± 0

  19. Hourly elemental concentrations in PM2.5 aerosols sampled simultaneously at urban background and road site during SAPUSS – diurnal variations and PMF receptor modelling

    Directory of Open Access Journals (Sweden)

    M. Dall'Osto

    2013-04-01

    Full Text Available Hourly-resolved aerosol chemical speciation data can be a highly powerful tool to determine the source origin of atmospheric pollutants in urban environments. Aerosol mass concentrations of seventeen elements (Na, Mg, Al, S, Cl, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Sr and Pb were obtained by time (1 h and size (PM2.5 particulate matter 2.5 mass fraction simultaneously measured at the UB and RS sites: (1 the regional aerosol sources impact both monitoring sites at similar concentrations regardless their different ventilation conditions; (2 by contrast, local industrial aerosol plumes associated with shipping oil combustion and smelters activities have a higher impact on the more ventilated UB site; (3 a unique source of Pb-Cl (associated with combustion emissions is found to be the major (82% source of fine Cl in the urban agglomerate; (4 the mean diurnal variation of PM2.5 primary traffic non-exhaust brake dust (Fe-Cu suggests that this source is mainly emitted and not resuspended, whereas PM2.5 urban dust (Ca is found mainly resuspended by both traffic vortex and sea breeze; (5 urban dust (Ca is found the aerosol source most affected by land wetness, reduced by a factor of eight during rainy days and suggesting that wet roads may be a solution for reducing urban dust concentrations.

  20. Long-term comparative study of columnar and surface mass concentration aerosol properties in a background environment

    Science.gov (United States)

    Bennouna, Y. S.; Cachorro, V. E.; Mateos, D.; Burgos, M. A.; Toledano, C.; Torres, B.; de Frutos, A. M.

    2016-09-01

    The relationship between columnar and surface aerosol properties is not a straightforward problem. The Aerosol Optical Depth (AOD), Ångström exponent (AE), and ground-level Particulate Matter (PMX, x = 10 or 2.5 μm) data have been studied from a climatological point of view. Despite the different meanings of AOD and PMx both are key and complementary quantities that quantify aerosol load in the atmosphere and many studies intend to find specific relationships between them. Related parameters such as AE and PM ratio (PR = PM2.5/PM10), giving information about the predominant particle size, are included in this study on the relationships between columnar and surface aerosol parameters. This study is based on long measurement records (2003-2014) obtained at two nearby background sites from the AERONET and EMEP networks in the north-central area of Spain. The climatological annual cycle of PMx shows two maxima along the year (one in late-winter/early-spring and another in summer), but this cycle is not followed by the AOD which shows only a summer maximum and a nearly bell shape. However, the annual means of both data sets show strong correlation (R = 0.89) and similar decreasing trends of 40% (PM10) and 38% (AOD) for the 12-year record. PM10 and AOD daily data are moderately correlated (R = 0.58), whereas correlation increases for monthly (R = 0.74) and yearly (R = 0.89) means. Scatter plots of AE vs. AOD and PR vs. PM10 have been used to characterize aerosols over the region. The PR vs. AE scatterplot of daily data shows no correlation due to the prevalence of intermediate-sized particles. As day-to-day correlation is low (especially for high turbidity events), a binned analysis was also carried out to establish consistent relationships between columnar and surface quantities, which is considered to be an appropriate approach for environmental and climate studies. In this way the link between surface concentrations and columnar remote sensing data is shown to

  1. Preliminary results of determination of chemical element concentrations in the aerosol of Venus clouds

    Science.gov (United States)

    Andreychikov, B. M.; Mukhin, L. M.; Korchuganov, B. N.; Akhmetshin, I. K.; Tokarev, Y. N.; Medvedev, A. V.; Goldfeld, M. N.; Faynboym, V. M.; Kalyuzhnyy, A. V.; Petryanov, I. V.

    1986-01-01

    An X-ray radiometeric experiment is described along with the results of measurements of the elemental composition of aerosols in Venusian clouds. A preliminary analysis of the data showed that sulfur is present in the range of heights 63 to 47 km with mean content of 5.8 mg/cu m and that chlorine is present in the height range 61 t0 52 km with a mean content of 4.1 mg/cu m. The results of measurements in the range 52 to 47 km may come to an agreement if phosphorus is present in the aerosol with a mean concentration of 7.7 mg/cu m.

  2. Marine boundary layer sea spray aerosol number concentrations during VOCALS-REx

    Science.gov (United States)

    BLOT, R. P.; Clarke, A. D.; Howell, S. G.; Kapustin, V. N.

    2012-12-01

    Marine boundary layer (MBL) sea spray aerosols include all the inorganic material (sea-salt), organic matter from biogenic activity (plankton, bacteria, microalgae) and other surface active material (exopolymer) found at the surface ocean. SSA are released into the MBL by bursting air bubbles originating from wind-induced breaking waves at the ocean surface. SSA play a major role in the Earth's radiative budget due to their ability to significantly scatter the solar radiation and because of their high hygroscopicity SSA are effective as cloud condensation nuclei (CCN), thereby influencing cloud droplet numbers. Early studies generally focused on sizes larger than about 0.2μm due to their influence on atmospheric light propagation and also because of the instrumental difficulty to distinguish SSA from the more numerous natural sulfate and fine anthropogenic aerosol. During the last two decades, evidence from laboratory and field experiments showed the existence of SSA aerosol down to 0.01μm . Even though ultrafine SSA (fraction of the size distribution that dominate CCN at low supersaturations characteristic of stratus clouds near 0.3%. We analyze thermally resolved airborne aerosol measurements made in the MBL during the VAMOS Ocean-Cloud-Atmosphere-Land-Study Regional Experiment (VOCALS-REx) over the the Southeast Pacific. We confirm that open-ocean SSA effective as CCN are produced from bubble bursting processes are present at dry sizes as small as 0.040μm.

  3. Evaluation and intercomparison of the aerosol number concentrations and CCNs in global models

    Science.gov (United States)

    Fanourgakis, Georgios; Myriokefalitakis, Stelios; Kanakidou, Maria; Makkonen, Risto; Grini, Alf; Stier, Philip; Watson-Parris, Duncan; Schutgens, Nick; Neubauer, David; Lohmann, Ulrike; Nenes, Athanasis

    2017-04-01

    In this work preliminary results of the current status of BACCHUS global modeling of aerosol number concentrations and cloud condensation nuclei (CCN) are presented and compared to observations. So far, simulation results from the TM4-ECPL, ECHAM-HAM, ECHAM6-HAM2 and NorESM models have become available. Hourly model results for the aerosol number concentrations and CCN concentrations at various supersaturation ratios, as well as their corresponding daily and monthly averaged values are compared to the measurements from nine ACTRIS sites for the years 2010-2015. CCN concentration persistence obtained from the auto-correlation function of observational and model data is compared. Seasonal variations are also considered in the present analysis. In order to identify any common biases against observations, the model results are further analyzed in terms of the particles chemical composition and the set of hygroscopicity parameters used for the calculation of CCNs. Annual mean surface-level number concentrations of various particle sizes and CCNs at 0.2% supersaturation predicted by the models along with their corresponding chemical composition are presented and discussed.

  4. Pan-Arctic enhancements of light absorbing aerosol concentrations due to North American boreal forest fires during summer 2004

    Science.gov (United States)

    Stohl, A.; Andrews, E.; Burkhart, J. F.; Forster, C.; Herber, A.; Hoch, S. W.; Kowal, D.; Lunder, C.; Mefford, T.; Ogren, J. A.; Sharma, S.; Spichtinger, N.; Stebel, K.; Stone, R.; StröM, J.; TøRseth, K.; Wehrli, C.; Yttri, K. E.

    2006-11-01

    During summer of 2004, about 2.7 million hectare of boreal forest burned in Alaska, the largest annual area burned on record, and another 3.1 million hectare burned in Canada. This study explores the impact of emissions from these fires on light absorbing aerosol concentration levels, aerosol optical depths (AOD), and albedo at the Arctic stations Barrow (Alaska), Alert (Canada), Summit (Greenland), and Zeppelin/Ny Ålesund on Spitsbergen (Norway). The Lagrangian particle dispersion model FLEXPART was run backward from these sites to identify periods that were influenced by forest fire pollution plumes. It is shown that the fires led to enhanced values of particle light absorption coefficients (σap) at all of these sites. Barrow, about 1000 km away from the fires, was affected by several fire pollution plumes, one leading to spectacularly high 3-hour mean σap values of up to 32 Mm-1, more than the highest values measured in Arctic Haze. AOD measurements for a wavelength of 500 nm saturated but were estimated at above 4-5 units, unprecedented in the station records. Fire plumes were transported through the atmospheric column over Summit continuously for 2 months, during which all measured AOD values were enhanced, with maxima up to 0.4-0.5 units. Equivalent black carbon concentrations at the surface at Summit were up to 600 ng m-3 during two major episodes, and Alert saw at least one event with enhanced σap values. FLEXPART results show that Zeppelin was located in a relatively unaffected part of the Arctic. Nevertheless, there was a 4-day period with daily mean σap > 0.3 Mm-1, the strongest episode of the summer half year, and enhanced AOD values. Elevated concentrations of the highly source-specific compound levoglucosan positively confirmed that biomass burning was the source of the aerosols at Zeppelin. In summary, this paper shows that boreal forest fires can lead to elevated concentrations of light absorbing aerosols throughout the entire Arctic. Enhanced

  5. Organic aerosol concentration and composition over Europe: insights from comparison of regional model predictions with aerosol mass spectrometer factor analysis

    Directory of Open Access Journals (Sweden)

    C. Fountoukis

    2014-03-01

    Full Text Available A detailed three-dimensional regional chemical transport model (PMCAMx was applied over Europe focusing on the formation and chemical transformation of organic matter. Three periods representative of different seasons were simulated, corresponding to intensive field campaigns. An extensive set of AMS measurements was used to evaluate the model and, using factor analysis results, gain more insight into the sources and transformations of organic aerosol (OA. Overall, the agreement between predictions and measurements for OA concentration is encouraging with the model reproducing two thirds of the data (daily average mass concentrations within a factor of two. Oxygenated OA (OOA is predicted to contribute 93% to total OA during May, 87% during winter and 96% during autumn with the rest consisting of fresh primary OA (POA. Predicted OOA concentrations compare well with the observed OOA values for all periods with an average fractional error of 0.53 and a bias equal to −0.07 (mean error = 0.9 μg m−3, mean bias = −0.2 μg m−3. The model systematically underpredicts fresh POA in most sites during late spring and autumn (mean bias up to −0.8 μg m−3. Based on results from a source apportionment algorithm running in parallel with PMCAMx, most of the POA originates from biomass burning (fires and residential wood combustion and therefore biomass burning OA is most likely underestimated in the emission inventory. The model performs well at all sites when the PMF-estimated low volatility OOA is compared against the OA with C* ≤ 0.1 μg m−3 and semivolatile OOA against the OA with C* > 0.1 μg m−3 respectively.

  6. A European aerosol phenomenology -4: Harmonized concentrations of carbonaceous aerosol at 10 regional background sites across Europe

    Science.gov (United States)

    Cavalli, F.; Alastuey, A.; Areskoug, H.; Ceburnis, D.; Čech, J.; Genberg, J.; Harrison, R. M.; Jaffrezo, J. L.; Kiss, G.; Laj, P.; Mihalopoulos, N.; Perez, N.; Quincey, P.; Schwarz, J.; Sellegri, K.; Spindler, G.; Swietlicki, E.; Theodosi, C.; Yttri, K. E.; Aas, W.; Putaud, J. P.

    2016-11-01

    Although particulate organic and elemental carbon (OC and EC) are important constituents of the suspended atmospheric particulate matter (PM), measurements of OC and EC are much less common and more uncertain than measurements of e.g. the ionic components of PM. In the framework of atmospheric research infrastructures supported by the European Union, actions have been undertaken to determine and mitigate sampling artefacts, and assess the comparability of OC and EC data obtained in a network of 10 atmospheric observatories across Europe. Positive sampling artefacts (from 0.4 to 2.8 μg C/m3) and analytical discrepancies (between -50% and +40% for the EC/TC ratio) have been taken into account to generate a robust data set, from which we established the phenomenology of carbonaceous aerosols at regional background sites in Europe. Across the network, TC and EC annual average concentrations range from 0.4 to 9 μg C/m3, and from 0.1 to 2 μg C/m3, respectively. TC/PM10 annual mean ratios range from 0.11 at a Mediterranean site to 0.34 at the most polluted continental site, and TC/PM2.5 ratios are slightly greater at all sites (0.15-0.42). EC/TC annual mean ratios range from 0.10 to 0.22, and do not depend much on PM concentration levels, especially in winter. Seasonal variations in PM and TC concentrations, and in TC/PM and EC/TC ratios, differ across the network, which can be explained by seasonal changes in PM source contributions at some sites.

  7. Continuous Measurement of Number Concentrations and Elemental Composition of Aerosol Particles for a Dust Storm Event in Beijing

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    A continuous measurement of number size distributions and chemical composition of aerosol particles was conducted in Beijing in a dust storm event during 21-26 March 2001. The number concentration of coarse particles (>2μm) increased more significantly than fine particles (<2μm) during the dust storm due to dust weather, while the anthropogenic aerosols collected during the non-dust-storm period tended to be associated with fine particles. Elemental compositions were analyzed by using proton-induced X-ray emission (PIXE). The results show that 20 elements in the dust storm were much higher than in the non-dust-storm period. The calculated soil dust concentration during the dust storm was, on average, 251.8μg m-3, while it was only 52.1 μg m-3 on non-dust-storm days. The enrichment factors for Mg, Al, P, K, Ca, Ti, Mn, Fe, Cl, Cu, Pb, and Zn show small variations between the dust storm and the non-dust-storm period, while those for Ca, Ni and Cr in the dust storm were much lower than those in the non-dust-storm period due to significant local emission sources. A high concentration and enrichment factor for S were observed during the dust storm, which implies that the dust particles were contaminated by aerosol particles from anthropogenic emissions during the long-range transport. A statistical analysis shows that the elemental composition of particles collected during the dust storm in Beijing were better correlated with those of desert soil colleted from desert regions in Inner Mongolia. Air mass back-trajectory analysis further confirmed that this dust storm event could be identified as streaks of dust plumes originating from Inner Mongolia.

  8. Aerosolized Antibiotics.

    Science.gov (United States)

    Restrepo, Marcos I; Keyt, Holly; Reyes, Luis F

    2015-06-01

    Administration of medications via aerosolization is potentially an ideal strategy to treat airway diseases. This delivery method ensures high concentrations of the medication in the targeted tissues, the airways, with generally lower systemic absorption and systemic adverse effects. Aerosolized antibiotics have been tested as treatment for bacterial infections in patients with cystic fibrosis (CF), non-CF bronchiectasis (NCFB), and ventilator-associated pneumonia (VAP). The most successful application of this to date is treatment of infections in patients with CF. It has been hypothesized that similar success would be seen in NCFB and in difficult-to-treat hospital-acquired infections such as VAP. This review summarizes the available evidence supporting the use of aerosolized antibiotics and addresses the specific considerations that clinicians should recognize when prescribing an aerosolized antibiotic for patients with CF, NCFB, and VAP.

  9. Temporal variations in elemental concentrations of atmospheric aerosols in Mexico City

    Energy Technology Data Exchange (ETDEWEB)

    Aldape U, F. [ININ, 52045 Ocoyoacac, Estado de Mexico (Mexico)

    1992-05-15

    Measurements are reported of elemental concentrations of airborne particulates in Mexico City and their time variation over a one-week period in the spring of 1988. Proton-induced X-ray emission analysis, PIXE, was used to analyse the atmospheric aerosols which were bombarded with 2.5 MeV protons from the 12 MV Tandem Van de Graaff accelerator at the National Institute of Nuclear Research, ININ. Variations in the elemental concentrations were observed over the time period studied. An intercomparison was made in the case of the element lead with PIXE results obtained at the Crocker Nuclear Laboratory, CNL, University of California for the same set of samples. Excellent agreement was obtained both for the time variation of the relative concentration and the absolute lead concentrations. These results give added confidence to the protocol adopted at ININ. (Author)

  10. Water-soluble organic carbon in urban aerosol: concentrations, size distributions and contribution to particulate matter

    Energy Technology Data Exchange (ETDEWEB)

    Timonen, H. J.; Saarikoski, S. K.; Aurela, M. A.; Saarnio, K. M.; Hillamo, R. E. (Finnish Meteorological Inst., Helsinki (Finland))

    2008-07-01

    The aim of this study was to characterize the concentrations and particle mass size distributions of water-soluble organic carbon (WSOC) in urban aerosols. The sample collection was carried out in spring 2006 at the SMEAR III station in Helsinki, Finland, by using a size-segregating method (MOUDI) and by collecting sub-micrometer fraction of aerosols on the filter. During the three-month measurement period, a major 12-day biomass burning pollution episode was observed. Concentrations of WSOC, organic carbon, monosaccharide anhydrides, inorganic ions and some organic acids (oxalic, succinic and malonic acid) were analyzed from the PM{sub 1} samples. The measured OC and WSOC concentrations varied in ranges 0.67-15.7 mug m-3 and 0.26-10.7 mug m3, respectively. The WSOC/OC concentration ratio was between 0.30 and 0.89 with an average of 0.54. Size distributions of WSOC, inorganic ions and total mass were determined from the MOUDI samples. WSOC had bimodal size distributions with a clear accumulation mode below 1 mum of particle aerodynamic diameter and minor coarse mode at sizes > 1 mum. (orig.)

  11. Opposite long-term trends in aerosols between low and high altitudes: a testimony to the aerosol-PBL feedback

    Science.gov (United States)

    Dong, Zipeng; Li, Zhanqing; Yu, Xing; Cribb, Maureen; Li, Xingmin; Dai, Jin

    2017-06-01

    Interactions between absorbing aerosols and the planetary boundary layer (PBL) play an important role in affecting air pollution near the surface. In this study, a unique feature of the aerosol-PBL interaction is identified that has important implications in monitoring and combating air pollution. Opposite trends in aerosol loading between the lower and upper PBL are shown on a wide range of timescales and data acquired by various platforms: from a short-term field experiment to decadal satellite observations and multidecadal ground observations in China. A novel method is proposed to obtain the vertical profiles of aerosol loading from passive sensors by virtue of varying elevations. The analyses of visibility, aerosol optical depth, and extinction with different temporal scales exhibit the similar trend, i.e., increasing in the lower atmosphere but decreasing in the upper atmosphere. Integration of the reversal aerosol trend below and above the PBL resulted in a much less change in the column-integrated quantities. The surface cooling effect, together with the change in the heating rate induced by the absorbing aerosol, unevenly modifies the atmospheric temperature profile, causing a more stable atmosphere inside the PBL but a destabilized atmosphere above the PBL. Such a change in the atmospheric stability favors the accumulation of pollutants near the surface and the vertical diffusion of aerosol particles in the upper atmosphere, both of which are consistent with the observed reversal aerosol trends. These findings have multiple implications in understanding and combating air pollution, especially in many developing countries with high emissions of light-absorbing aerosols.

  12. First measurements of reactive α-dicarbonyl concentrations on PM2.5 aerosol over the boreal forest in Finland during HUMPPA-COPEC 2010 – source apportionment and links to aerosol aging

    Directory of Open Access Journals (Sweden)

    T. Petäjä

    2012-01-01

    Full Text Available The first dataset for summertime boreal forest concentrations of two atmospherically relevant α-dicarbonyl compounds, glyoxal (Gly and methylglyoxal (Mgly on PM2.5 aerosol was obtained during the HUMPPA-COPEC-2010 field measurement intensive in Hyytiälä, Finland. Identification of anthropogenic influences over the course of the campaign, using trace gas signatures and aerosol particle chemical composition analysis, allowed the identification of different events such as urban pollution plumes, biomass burning and sawmill emissions as sources of high Gly and Mgly concentrations. Mean aerosol concentrations during periods of biogenic influence were 0.81 ng m−3 for Gly and 0.31 ng m−3 for Mgly. Mgly was generally less abundant in PM2.5, probably due to its shorter photolysis lifetime and less effective partitioning into the particle phase due to its smaller effective Henry's Law constant compared to Gly. This is in contrast with previous urban studies which show significantly more Mgly than Gly. Peak concentrations for Gly coincided with nearby sources, e.g. high VOC emissions from nearby sawmills, urban pollution plumes from the city of Tampere located 50 km southwest of the sampling site and biomass burning emissions from wildfires. Calculated ratios of Gly in PM2.5 and total organic matter in PM1 aerosols indicate higher values in less aged aerosols. Irreversible processing of Gly in the particle phase, e.g. via oxidation by OH radicals, organo sulfate or imidazole formation are processes currently discussed in the literature which could likely explain these findings.

  13. Ambient Observations of Organic Nitrogen Compounds in Submicrometer Aerosols in New York Using High Resolution Aerosol Mass Spectrometry

    Science.gov (United States)

    Zhou, S.; Ge, X.; Xu, J.; Sun, Y.; Zhang, Q.

    2015-12-01

    Organic nitrogen (ON) compounds, which include amines, nitriles, organic nitrates, amides, and N-containing aromatic heterocycles, are an important class of compounds ubiquitously detected in atmospheric particles and fog and cloud droplets. Previous studies indicate that these compounds can make up a significant fraction (20-80%) of the total nitrogen (N) content in atmospheric condensed phases and play important roles in new particle formation and growth and affecting the optical and hygroscopicity of aerosols. In this study, we report the observation of ON compounds in submicrometer particles (PM1) at two locations in New York based on measurements using Aerodyne high-resolution time-of-flight mass spectrometer (HR-ToF-AMS). One study was conducted as part of the US Department of Energy funded Aerosol Lifecyle - Intensive Operation Period (ALC-IOP) campaign at Brookhaven National Lab (BNL, 40.871˚N, 72.89˚W) in summer, 2011 and the other was conducted at the Queen's College (QC) in New York City (NYC) in summer, 2009. We observed a notable amount of N-containing organic fragment ions, CxHyNp+ and CxHyOzNp+, in the AMS spectra of organic aerosols at both locations and found that they were mainly associated with amino functional groups. Compared with results from lab experiments, the C3H8N+ at m/z = 58 was primarily attributed to trimethylamine. In addition, a significant amount of organonitrates was observed at BNL. Positive matrix factorization (PMF) analysis of the high resolution mass spectra (HRMS) of organic aerosols identified a unique nitrogen-enriched OA (NOA) factor with elevated nitrogen-to-carbon (N/C) at both BNL and QC. Analysis of the size distributions, volatility profiles, and correlations with external tracer indicates that acid-base reactions of amino compounds with sulfate and acidic gas were mainly responsible for the formation of amine salts. Photochemical production was also observed to play a role in the formation of NOA. Bivariate polar

  14. Aerosol Number Concentrations and Visibility during Dense Fog over a Subtropical Urban Site

    Directory of Open Access Journals (Sweden)

    Manju Mohan

    2014-01-01

    Full Text Available There is now enough evidence of greater frequencies and extent of fog formation in urban areas. These could easily be linked to rapid increase in aerosol number concentration (ANC peculiar to polluted urban environments. It is therefore pertinent to study ANC and visibility alongside the meteorological parameters in order to investigate the relationships which may possibly exist between these parameters especially during foggy conditions. This study based on field measurements of ANC for aerosol spectrum varying from 0.3 µm to 20 µm attempts to investigates whether a threshold ANC could be associated with a given visibility range during low visibility conditions including dense fog episodes. Thus, the present work explores relationship between ANC size spectrum and visibility (100 m–4500 m in a polluted urban environment in India with specific reference to episodes of dense fog during winter period. The study depicts a threshold minimum value of ANC during foggy conditions. A power relationship between ANC and visibility is obtained. Further, aerosol number distribution and size distribution function are also studied and empirical relation is compared with previous studies. Further work is suggested to strengthen the findings presented here.

  15. Separating Dust Mixtures and Other External Aerosol Mixtures Using Airborne High Spectral Resolution Lidar Data

    Science.gov (United States)

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

    2013-12-01

    Knowledge of aerosol type is important for source attribution and for determining the magnitude and assessing the consequences of aerosol radiative forcing. The NASA Langley Research Center airborne High Spectral Resolution Lidar (HSRL-1) has acquired considerable datasets of both aerosol extensive parameters (e.g. aerosol optical depth) and intensive parameters (e.g. aerosol depolarization ratio, lidar ratio) that can be used to infer aerosol type. An aerosol classification methodology has been used extensively to classify HSRL-1 aerosol measurements of different aerosol types including dust, smoke, urban pollution, and marine aerosol. However, atmospheric aerosol is frequently not a single pure type, but instead occurs as a mixture of types, and this mixing affects the optical and radiative properties of the aerosol. Here we present a comprehensive and unified set of rules for characterizing external mixtures using several key aerosol intensive parameters: extinction-to-backscatter ratio (i.e. lidar ratio), backscatter color ratio, and depolarization ratio. Our mixing rules apply not just to the scalar values of aerosol intensive parameters, but to multi-dimensional normal distributions with variance in each measurement dimension. We illustrate the applicability of the mixing rules using examples of HSRL-1 data where mixing occurred between different aerosol types, including advected Saharan dust mixed with the marine boundary layer in the Caribbean Sea and locally generated dust mixed with urban pollution in the Mexico City surroundings. For each of these cases we infer a time-height cross section of mixing ratio along the flight track and we partition aerosol extinction into portions attributed to the two pure types. Since multiple aerosol intensive parameters are measured and included in these calculations, the techniques can also be used for cases without significant depolarization (unlike similar work by earlier researchers), and so a third example of a

  16. Long-Term Observations on Aerosol Elemental Carbon and Mass Concentrations in Winter-Time in New Delhi: Implications for Local Source Changes

    Science.gov (United States)

    Aggarwal, S. G.; Singh, K.; Singh, N.; Gupta, P. K.

    2009-12-01

    Fossil-fuel and bio-fuel burning are the two major sources identified for high carbonaceous aerosol loadings in several mega cities in India. In the last decade, according to a report from the Central Pollution Control Board (CPCB, 1999), the vehicular emission (mostly diesel-powered engines) was contributed to ~67% of the total air pollution load in New Delhi. Therefore, a policy decision was taken by the government, and most of the diesel-powered engines were converted to compressed natural gas (CNG) -powered engines by 2003. To better understand the effect of these changes on air quality, we collected high volume aerosol samples (total suspended particles, TSP) mostly for a day basis at our institute building in New Delhi almost everyday during winter season (November to January) from 2002 to 2008. We found very high mean aerosol loading, i.e., 488±47 μg m-3 in 2002 winter, which dropped significantly to 280±73 μg m-3 in 2003 winter. Thereafter, a steadily increased trend of aerosol mass loadings was observed, i.e., 339±112, 339±120, 412±107 and 444±55 μg m-3 in 2004, 2005, 2006 and 2007 winters, respectively. Similar trend was also observed for elemental carbon (EC) concentration in TSP, which was peaked in 2002 (47±11 μg m-3) and minimized in 2003 (32±6 μg m-3), and then gradually increased to 41±8 μg m-3 in 2007 winter. These decline trends of aerosol mass and EC concentrations in 2003 can be explained well, because of the conversion of diesel engine to CNG engines of public transport facilities. However, again increase in aerosol mass and EC concentrations possibly because of a high increase in road traffic in recent years. According to the economic survey of New Delhi 2008-09, the number of vehicles (which includes all types of engines, i.e., petrol, diesel and CNG) has grown from ~3.3 millions in 1997-98 to ~5.6 millions in 2007-08. The influence of engine types and vehicle population on aerosol loading can also be explained well by SO2 and

  17. Concentration Effects and Ion Properties Controlling the Fractionation of Halides during Aerosol Formation

    Science.gov (United States)

    Guzman, Marcelo I.; Athalye, Richa R.; Rodriguez, Jose M.

    2012-01-01

    During the aerosolization process at the sea surface, halides are incorporated into aerosol droplets, where they may play an important role in tropospheric ozone chemistry. Although this process may significantly contribute to the formation of reactive gas phase molecular halogens, little is known about the environmental factors that control how halides selectively accumulate at the air-water interface. In this study, the production of sea spray aerosol is simulated using electrospray ionization (ESI) of 100 nM equimolar solutions of NaCl, NaBr, NaI, NaNO2, NaNO3, NaClO4, and NaIO4. The microdroplets generated are analyzed by mass spectrometry to study the comparative enrichment of anions (f (Isub x-)) and their correlation with ion properties. Although no correlation exists between f (sub x-) and the limiting equivalent ionic conductivity, the correlation coefficient of the linear fit with the size of the anions R(sub x-), dehydration free-energy ?Gdehyd, and polarizability alpha, follows the order: (R(sub x-)(exp -2)) > (R(sub x-)(exp -1)) >(R(sub x-) > delta G(sub dehyd) > alpha. The same pure physical process is observed in H2O and D2O. The factor f (sub x-) does not change with pH (6.8-8.6), counterion (Li+, Na+, K+, and Cs+) substitution effects, or solvent polarity changes in methanol - and ethanol-water mixtures (0 surfactant is used to modify the structure of the interface. Despite the observed enrichment of I- on the air-water interface of equimolar solutions, our results of seawater mimic samples agree with a model in which the interfacial composition is increasingly enriched in I- < Br- < Cl- over the oceanic boundary layer due to concentration effects in sea spray aerosol formation.

  18. Variability of aerosol particle number concentrations observed over the western Pacific in the spring of 2009

    Science.gov (United States)

    Takegawa, N.; Moteki, N.; Oshima, N.; Koike, M.; Kita, K.; Shimizu, A.; Sugimoto, N.; Kondo, Y.

    2014-12-01

    Airborne measurements of aerosols were conducted over the western Pacific in the spring of 2009 during the Aerosol Radiative Forcing in East Asia (A-FORCE) aircraft campaign. The A-FORCE flights intensively covered an important vertical-latitudinal range in the outflow region of East Asia (0-9 km altitude; 27°N-38°N). This paper presents the variability of aerosol particle number concentrations obtained by condensation particle counters and a Single-Particle Soot Photometer (SP2), with the focus on those in the free troposphere. The number concentration data include total condensation nuclei with particle diameters (dp) larger than 10 nm (total CN10), PM0.17-CN10 (dp 10-130 nm), and SP2 black carbon (NBC; dp 75-850 nm). Large increases in total CN10 that were not associated with NBC were observed in the free troposphere, suggesting influences from new particle formation (NPF). Statistical characteristics of total CN10, PM0.17-CN10, and NBC in the lower troposphere (LT; 0-3 km), middle troposphere (MT; 3-6 km), and upper troposphere (UT; 6-9 km) are investigated. The correlation between total CN10 and NBC, along with the ratio of PM0.17 to total CN10 and carbon monoxide mixing ratio (CO), is used to interpret the observed variability. The median concentrations of total CN10 and PM0.17-CN10 in the UT were higher than those in the MT by a factor of 1.4 and 1.6, respectively. We attribute the enhancements of CN10 in the UT to NPF. Possible mechanisms affecting NPF in the free troposphere are discussed.

  19. Biological aerosol particle concentrations and size distributions measured in pristine tropical rainforest air during AMAZE-08

    OpenAIRE

    J. A. Huffman; Sinha, B.; R. M. Garland; A. Snee-Pollmann; Gunthe, S. S.; Artaxo, P.; S. T. Martin; Andreae, M. O.; U. Pöschl

    2012-01-01

    As a part of the AMAZE-08 campaign during the wet season in the rainforest of Central Amazonia, an ultraviolet aerodynamic particle sizer (UV-APS) was operated for continuous measurements of fluorescent biological aerosol particles (FBAP). In the coarse particle size range (> 1 μm) the campaign median and quartiles of FBAP number and mass concentration were 7.3 × 104 m−3 (4.0–13.2 × 104 m&m...

  20. Simulation of particle size distribution with a global aerosol model: contribution of nucleation to aerosol and CCN number concentrations

    Directory of Open Access Journals (Sweden)

    F. Yu

    2009-04-01

    Full Text Available An advanced particle microphysics model with a number of computationally efficient schemes has been incorporated into a global chemistry transport model (GEOS-Chem to simulate particle number size distributions and cloud condensation nuclei (CCN concentrations in the atmosphere. Size-resolved microphysics for secondary particles (i.e., those formed from gaseous species and sea salt has been treated in the present study. The growth of nucleated particles through the condensation of sulfuric acid vapor and equilibrium uptake of nitrate, ammonium, and secondary organic aerosol is explicitly simulated, along with the scavenging of secondary particles by primary particles (dust, black carbon, organic carbon, and sea salt. We calculate secondary particle formation rate based on ion-mediated nucleation (IMN mechanism and constrain the parameterizations of primary particle emissions with various observations. Our simulations indicate that secondary particles formed via IMN appear to be able to account for the particle number concentrations observed in many parts of troposphere. A comparison of the simulated annual mean concentrations of condensation nuclei larger than 10 nm (CN10 with those measured values show very good agreement (within a factor of two in near all 22 sites around the globe that have at least one full year of CN10 measurements. Secondary particles appear to dominate the number abundance in most parts of the troposphere. Calculated CCN concentration at supersaturation of 0.4% (CCN0.4 and the fraction of CCN0.4 that is secondary (fCCNsec have large spatial variations. Over the middle latitude in the Northern Hemisphere, zonally averaged CCN0.4 decreases from ~400–700 cm−3 in the boundary layer (BL to below 100 cm−3 above altitude of ~4 km, the corresponding fCCNsec values change from 50–60% to above ~70%. In the Southern Hemisphere, the zonally

  1. Simulation of particle size distribution with a global aerosol model: contribution of nucleation to aerosol and CCN number concentrations

    Directory of Open Access Journals (Sweden)

    F. Yu

    2009-10-01

    Full Text Available An advanced particle microphysics model with a number of computationally efficient schemes has been incorporated into a global chemistry transport model (GEOS-Chem to simulate particle number size distributions and cloud condensation nuclei (CCN concentrations in the atmosphere. Size-resolved microphysics for secondary particles (i.e., those formed from gaseous species and sea salt has been treated in the present study. The growth of nucleated particles through the condensation of sulfuric acid vapor and equilibrium uptake of nitrate, ammonium, and secondary organic aerosol is explicitly simulated, along with the scavenging of secondary particles by primary particles (dust, black carbon, organic carbon, and sea salt. We calculate secondary particle formation rate based on ion-mediated nucleation (IMN mechanism and constrain the parameterizations of primary particle emissions with various observations. Our simulations indicate that secondary particles formed via IMN appear to be able to account for the particle number concentrations observed in many parts of the troposphere. A comparison of the simulated annual mean concentrations of condensation nuclei larger than 10 nm (CN10 with those measured values show very good agreement (within a factor of two in near all 22 sites around the globe that have at least one full year of CN10 measurements. Secondary particles appear to dominate the number abundance in most parts of the troposphere. Calculated CCN concentration at supersaturation of 0.4% (CCN0.4 and the fraction of CCN0.4 that is secondary (fsecCCN have large spatial variations. Over the middle latitude in the Northern Hemisphere, zonally averaged CCN0.4 decreases from ~400–700 cm−3 in the boundary layer (BL to below 100 cm−3 above altitude of ~4 km, the corresponding fsecCCN values change from 50–60% to above ~70%. In the Southern Hemisphere, the zonally

  2. Highly reactive free radicals in electronic cigarette aerosols.

    Science.gov (United States)

    Goel, Reema; Durand, Erwann; Trushin, Neil; Prokopczyk, Bogdan; Foulds, Jonathan; Elias, Ryan J; Richie, John P

    2015-09-21

    Electronic cigarette (EC) usage has increased exponentially, but limited data are available on its potential harmful effects. We tested for the presence of reactive, short-lived free radicals in EC aerosols by electron paramagnetic resonance spectroscopy (EPR) using the spin-trap phenyl-N-tert-butylnitrone (PBN). Radicals were detected in aerosols from all ECs and eliquids tested (2.5 × 10(13) to 10.3 × 10(13) radicals per puff at 3.3 V) and from eliquid solvents propylene glycol and glycerol and from "dry puffing". These results demonstrate, for the first time, the production of highly oxidizing free radicals from ECs which may present a potential toxicological risk to EC users.

  3. Aerosol characteristics in a mature coniferous forest—Methodology, composition, sources and spatial concentration variations

    Science.gov (United States)

    Wiman, Bo L. B.; Lannefors, Hans O.

    A forest site in southern Sweden representative of a wider range of coniferous forest Londscapes has been characterized with respect to aerosol composition (NO -3, S, Cl, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn. Br and Pb). In one series aerosol sampling was carried out simultaneously along a horizontal transect with four stations, one located in open field, one at the forest edge and two within the forest. In another series simultaneous sampling was performed along a vertical transect with four sampling points, one located below but near the canopy top and the others further downwards through the canopy (height c. 25 m). Sampling strategy and analytical methods are presented in detail. Statistical analyses of concentration data suggest that K, Ca, Ti, Mn and Fe in the coarse particle fractions originated from soil, whereas other components (S, V, Cu and Pb) were of mainly anthropogenic origin. Depletion of coarse fraction concentrations within the forest was detected for several elements, whereas spatial variations of fine fraction concentrations showed weak or no systematic trends. This result is interpreted as a net effect of counteracting mechanisms in the forest: losses due to deposition and inputs due to turbulence and gravitationally settling particles.

  4. Acid and organic aerosol coatings on magnetic nanoparticles increase iron concentrations in human airway epithelial cells.

    Science.gov (United States)

    Ghio, Andrew J; Dailey, Lisa A; Richards, Judy H; Jang, Myoseon

    2009-07-01

    Numerous industrial applications for man-made nanoparticles have been proposed. Interactions of nanoparticles with agents in the atmosphere may impact human health. We tested the postulate that in vitro exposures of respiratory epithelial cells to airborne magnetic nanoparticles (MNP; Fe(3)O(4)) with and without a secondary organic aerosol (SOA) and an inorganic acid could affect iron homeostasis, oxidative stress, and interleukin (IL)-8 release. Cell iron concentrations were increased after exposures to MNP and values were further elevated with co-exposures to either SOA or inorganic acid. Increased expression of ferritin and elevated levels of RNA for DMT1, proteins for iron storage and transport respectively, followed MNP exposures, but values were significant for only those with co-exposures to inorganic acid and organic aerosols. Cell iron concentration corresponded to a measure of oxidative stress in the airway epithelial cells; MNP with co-exposures to SOA and inorganic acid increased both available metal and indices of oxidant generation. Finally, the release of a proinflammatory cytokine (i.e. IL-8) by the exposed cells similarly increased with cell iron concentration. We conclude that MNP can interact with a SOA and an inorganic acid to present metal in a catalytically reactive state to cultured respiratory cells. This produces an oxidative stress to affect a release of IL-8.

  5. Size-resolved morphological properties of the high Arctic summer aerosol during ASCOS-2008

    Science.gov (United States)

    Hamacher-Barth, Evelyne; Leck, Caroline; Jansson, Kjell

    2016-05-01

    The representation of aerosol properties and processes in climate models is fraught with large uncertainties. Especially at high northern latitudes a strong underprediction of aerosol concentrations and nucleation events is observed and can only be constrained by in situ observations based on the analysis of individual aerosol particles. To further reduce the uncertainties surrounding aerosol properties and their potential role as cloud condensation nuclei this study provides observational data resolved over size on morphological and chemical properties of aerosol particles collected in the summer high Arctic, north of 80° N. Aerosol particles were imaged with scanning and transmission electron microscopy and further evaluated with digital image analysis. In total, 3909 aerosol particles were imaged and categorized according to morphological similarities into three gross morphological groups: single particles, gel particles, and halo particles. Single particles were observed between 15 and 800 nm in diameter and represent the dominating type of particles (82 %). The majority of particles appeared to be marine gels with a broad Aitken mode peaking at 70 nm and accompanied by a minor fraction of ammonium (bi)sulfate with a maximum at 170 nm in number concentration. Gel particles (11 % of all particles) were observed between 45 and 800 nm with a maximum at 154 nm in diameter. Imaging with transmission electron microscopy allowed further morphological discrimination of gel particles in "aggregate" particles, "aggregate with film" particles, and "mucus-like" particles. Halo particles were observed above 75 nm and appeared to be ammonium (bi)sulfate (59 % of halo particles), gel matter (19 %), or decomposed gel matter (22 %), which were internally mixed with sulfuric acid, methane sulfonic acid, or ammonium (bi)sulfate with a maximum at 161 nm in diameter. Elemental dispersive X-ray spectroscopy analysis of individual particles revealed a prevalence of the monovalent

  6. Levoglucosan indicates high levels of biomass burning aerosols over oceans from the Arctic to Antarctic

    Science.gov (United States)

    Hu, Q.; Xie, Z.; Wang, X.; Kang, H.; Zhang, P.

    2015-12-01

    Biomass burning discharges numerous kinds of gases and aerosols, such as carbon dioxide (CO2), carbon monoxide (CO), methane (CH4), black carbon (BC), alcohols, organic acids and persistent organic pollutants (POPs), and is known to affect air quality, global carbon cycle, and climate. However, the extent to which biomass burning gases/aerosols are present on a global scale, especially in the marine atmosphere, is poorly understood. Here we measure levoglucosan, a superior molecular tracer of biomass burning aerosols because of its single source, in marine air from the Arctic Ocean through the North and South Pacific Ocean to coastal Antarctica during burning season. Levoglucosan was found to be present in all regions at ng/m3 levels. As a whole, levoglucosan concentrations in the Southern Hemisphere were comparable to those in the Northern Hemisphere. Marine air in the mid-latitudes (30°-60° N and S) has the highest levoglucosan loading due to the emission from adjacent lands. Air over the Arctic Ocean which affected by biomass burning in the east Siberia has intermediate loading. Equatorial latitudes is the main source of biomass burning emissions, however, levoglucosan is in relatively low level. Large amount of precipitation and high hydroxyl radical concentration in this region cause more deposition and degradation of levoglucosan during transport. Previous studies were debatable on the influence of biomass burning on the Antarctic because of uncertain source of BC. Here via levoglucosan, it is proved that although far away from emission sources, the Antarctic is still affected by biomass burning aerosols which may be derived from South America. Biomass burning has a significant impact on mercury (Hg) and water-soluble organic carbon (WSOC) in marine aerosols from pole to pole, with more contribution to WSOC in the Northern Hemisphere than in the Southern Hemisphere.

  7. Enhancing non-refractory aerosol apportionment from an urban industrial site through receptor modelling of complete high time-resolution aerosol mass spectra

    Directory of Open Access Journals (Sweden)

    M. L. McGuire

    2014-02-01

    Full Text Available Receptor modelling was performed on quadrupole unit mass resolution aerosol mass spectrometer (Q-AMS sub-micron particulate matter (PM chemical speciation measurements from Windsor, Ontario, an industrial city situated across the Detroit River from Detroit, Michigan. Aerosol and trace gas measurements were collected on board Environment Canada's CRUISER mobile laboratory. Positive matrix factorization (PMF was performed on the AMS full particle-phase mass spectrum (PMFFull MS encompassing both organic and inorganic components. This approach was compared to the more common method of analysing only the organic mass spectra (PMFOrg MS. PMF of the full mass spectrum revealed that variability in the non-refractory sub-micron aerosol concentration and composition was best explained by six factors: an amine-containing factor (Amine; an ammonium sulphate and oxygenated organic aerosol containing factor (Sulphate-OA; an ammonium nitrate and oxygenated organic aerosol containing factor (Nitrate-OA; an ammonium chloride containing factor (Chloride; a hydrocarbon-like organic aerosol (HOA factor; and a moderately oxygenated organic aerosol factor (OOA. PMF of the organic mass spectrum revealed three factors of similar composition to some of those revealed through PMFFull MS: Amine, HOA and OOA. Including both the inorganic and organic mass proved to be a beneficial approach to analysing the unit mass resolution AMS data for several reasons. First, it provided a method for potentially calculating more accurate sub-micron PM mass concentrations, particularly when unusual factors are present, in this case, an Amine factor. As this method does not rely on a priori knowledge of chemical species, it circumvents the need for any adjustments to the traditional AMS species fragmentation patterns to account for atypical species, and can thus lead to more complete factor profiles. It is expected that this method would be even more useful for HR-ToF-AMS data, due to

  8. Aerosol classification using airborne High Spectral Resolution Lidar measurements – methodology and examples

    Directory of Open Access Journals (Sweden)

    S. P. Burton

    2012-01-01

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

  9. Physical and optical characteristics of atmospheric aerosols during ICARB at Manora Peak, Nainital: A sparsely inhabited, high-altitude location in the Himalayas

    Indian Academy of Sciences (India)

    U C Dumka; K Krishna Moorthy; P Pant; P Hegde; Ram Sagar; K Pandey

    2008-07-01

    Collocated measurements of the optical and physical properties of columnar and near-surface aerosols were carried out from Manora Peak, Nainital (a sparsely inhabited, high altitude location, ∼2km above mean sea level, in the Himalayas), during the Integrated Campaign for Aerosols, gases and Radiation Budget (ICARB) under the Geosphere Biosphere Programme of the Indian Space Research Organization (ISRO-GBP). Under this, observational data of spectral aerosol optical depths (AOD), mass concentration of aerosol black carbon (B), mass concentration () and number concentration () of composite (total) aerosols near the surface and meteorological parameters were collected during the period February 15 to April 30, 2006. Though very low (> 0.1 at 500 nm) AODs were observed during clear days, as much as a fourfold increase was seen on hazy days. The Ångström exponent (), deduced from the spectral AODs, revealed high values during clear days, while on hazy days was low; with an overall mean value of 0.69 ± 0.06 for the campaign period. BC mass concentration varied between 0.36 and 2.87 g m−3 and contributed in the range 0.7 to 1.8% to the total aerosol mass. Total aerosol number concentration and BC mass concentration showed diurnal variation with a midnight and early morning minimum and a late afternoon maximum; a pattern quite opposite to that seen in low altitude stations. These are attributed to the dynamics of the atmospheric boundary layer.

  10. High-efficiency solar concentrator

    Science.gov (United States)

    Lansing, F. L.; Dorman, J.

    1980-01-01

    A new type of solar concentrator is presented using liquid lenses and simple translational tracking mechanism. The concentrator achieves a 100:1 nominal concentration ratio and is compared in performance with a flat-plate collector having two sheets of glazing and non-selective coating. The results of the thermal analysis show that higher temperatures can be obtained with the concentrator than is possible with the non-concentrator flat-plate type. Furthermore, the thermal efficiency far exceeds that of the comparative flat-plate type for all operating conditions.

  11. Evaluation of the tropospheric aerosol number concentrations simulated by two versions of the global model ECHAM5-HAM

    Science.gov (United States)

    Zhang, K.; Kazil, J.; Feichter, J.

    2009-04-01

    Since its first version developed by Stier et al. (2005), the global aerosol-climate model ECHAM5-HAM has gone through further development and updates. The changes in the model include (1) a new time integration scheme for the condensation of the sulfuric acid gas on existing particles, (2) a new aerosol nucleation scheme that takes into account the charged nucleation caused by cosmic rays, and (3) a parameterization scheme explicitly describing the conversion of aerosol particles to cloud nuclei. In this work, simulations performed with the old and new model versions are evaluated against some measurements reported in recent years. The focus is on the aerosol size distribution in the troposphere. Results show that modifications in the parameterizations have led to significant changes in the simulated aerosol concentrations. Vertical profiles of the total particle number concentration (diameter > 3nm) compiled by Clarke et al. (2002) suggest that, over the Pacific in the upper free troposphere, the tropics are associated with much higher concentrations than the mid-latitude regions. This feature is more reasonably reproduced by the new model version, mainly due to the improved results of the nucleation mode aerosols. In the lower levels (2-5 km above the Earth's surface), the number concentrations of the Aitken mode particles are overestimated compared to both the Pacific data given in Clarke et al. (2002) and the vertical profiles over Europe reported by Petzold et al. (2007). The physical and chemical processes that have led to these changes are identified by sensitivity tests. References: Clarke and Kapustin: A Pacific aerosol survey - part 1: a decade of data on production, transport, evolution and mixing in the troposphere, J. Atmos. Sci., 59, 363-382, 2002. Petzold et al.: Perturbation of the European free troposphere aerosol by North American forest fire plumes during the ICARTT-ITOP experiment in summer 2004, Atmos. Chem. Phys., 7, 5105-5127, 2007

  12. Aerosol black carbon characteristics over a high-altitude Western Ghats location in Southern India

    Science.gov (United States)

    Udayasoorian, C.; Jayabalakrishnan, R. M.; Suguna, A. R.; Gogoi, Mukunda M.; Babu, S. Suresh

    2014-10-01

    Aerosol black carbon (BC) mass concentrations were continuously monitored over a period of 2 years (April 2010 to May 2012) from a high-altitude location Ooty in the Nilgiris Mountain range in southern India to characterize the distinct nature of absorbing aerosols and their seasonality. Despite being remote and sparsely inhabited, BC concentrations showed significant seasonality with higher values (~ 0.96 ± 0.35 μg m-3) in summer (March to May), attributed to increased vertical transport of effluents in the upwind valley regions, which might have been confined to the surrounding valley regions within the very shallow winter boundary layer. The local atmospheric boundary layer (ABL) influence in summer was further modulated by the long-range transported aerosols from the eastern locations of Ooty. During monsoon (June-August), the concentrations were far reduced (~ 0.23 ± 0.06 μg m-3) due to intense precipitation. Diurnal variations were found conspicuous mainly during summer season associated with local ABL. The spectral absorption coefficients (αabs) depicted, in general, flatter distribution (mostly < 1.0 for more than 85% of daily mean values), suggesting the relative dominance of fossil fuel combustion, though showed marginal seasonal change with higher values of αabs in summer.

  13. OH-initiated heterogeneous aging of highly oxidized organic aerosol

    Energy Technology Data Exchange (ETDEWEB)

    Kessler, Sean H.; Nah, Theodora; Daumit, Kelly E.; Smith, Jared D.; Leone, Stephen R.; Kolb, Charles E.; Worsnop, Douglas R.; Wilson, Kevin R.; Kroll, Jesse H.

    2011-12-05

    The oxidative evolution (“aging”) of organic species in the atmosphere is thought to have a major influence on the composition and properties of organic particulate matter, but remains poorly understood, particularly for the most oxidized fraction of the aerosol. Here we measure the kinetics and products of the heterogeneous oxidation of highly oxidized organic aerosol, with an aim of better constraining such atmospheric aging processes. Submicron particles composed of model oxidized organics—1,2,3,4-butanetetracarboxylic acid (C{sub 8}H{sub 10}O{sub 8}), citric acid (C{sub 6}H{sub 8}O{sub 7}), tartaric acid (C{sub 4}H{sub 6}O{sub 6}), and Suwannee River fulvic acid—were oxidized by gas-phase OH in a flow reactor, and the masses and elemental composition of the particles were monitored as a function of OH exposure. In contrast to our previous studies of less-oxidized model systems (squalane, erythritol, and levoglucosan), particle mass did not decrease significantly with heterogeneous oxidation. Carbon content of the aerosol always decreased somewhat, but this mass loss was approximately balanced by an increase in oxygen content. The estimated reactive uptake coefficients of the reactions range from 0.37 to 0.51 and indicate that such transformations occur at rates corresponding to 1-2 weeks in the atmosphere, suggesting their importance in the atmospheric lifecycle of organic particulate matter.

  14. AGLITE: a multiwavelength lidar for aerosol size distributions, flux, and concentrations

    Science.gov (United States)

    Wilkerson, Thomas D.; Zavyalov, Vladimir V.; Bingham, Gail E.; Swasey, Jason A.; Hancock, Jed J.; Crowther, Blake G.; Cornelsen, Scott S.; Marchant, Christian; Cutts, James N.; Huish, David C.; Earl, Curtis L.; Andersen, Jan M.; Cox, McLain L.

    2006-05-01

    We report on the design, construction and operation of a new multiwavelength lidar developed for the Agricultural Research Service of the United States Department of Agriculture and its program on particle emissions from animal production facilities. The lidar incorporates a laser emitting simultaneous, pulsed Nd laser radiation at 355, 532 and 1064 nm at a PRF of 10 kHz. Lidar backscatter and extinction data are modeled to extract the aerosol information. All-reflective optics combined with dichroic and interferometric filters permit all the wavelength channels to be measured simultaneously, day or night, using photon counting by PMTs, an APD, and high speed scaling. The lidar is housed in a transportable trailer for all-weather operation at any accessible site. The laser beams are directed in both azimuth and elevation to targets of interest. We describe application of the lidar in a multidisciplinary atmospheric study at a swine production farm in Iowa. Aerosol plumes emitted from the hog barns were prominent phenomena, and their variations with temperature, turbulence, stability and feed cycle were studied, using arrays of particle samplers and turbulence detectors. Other lidar measurements focused on air motion as seen by long duration scans of the farm region. Successful operation of this lidar confirms the value of multiwavelength, eye-safe lidars for agricultural aerosol measurements.

  15. Sensitivity of cloud albedo to aerosol concentration and spectral dispersion of cloud droplet size distribution

    Energy Technology Data Exchange (ETDEWEB)

    Iorga, G. [Faculty of Chemistry, University of Bucharest, Bucharest (Romania)]. E-mail: giorga@gw-chimie.math.unibuc.ro; Stefan, S. [Faculty of Physics, University of Bucharest, Bucharest (Romania)

    2007-07-15

    Both the enhancement of the aerosol number concentration and the relative dispersion of the cloud droplet size distribution (spectral dispersion) on a regional scale can modify the cloud reflectivity. This work is focused on the role that pre-cloud aerosol plays in cloud reflectivity. Log-normal aerosol size distributions were used to describe two aerosol types: marine and rural. The number of aerosols that activate to droplets was obtained based on Abdul-Razzak and Ghan's (2000) activation parameterization. The cloud albedo taking into account the spectral dispersion effect in the parameterization of cloud effective radius and in the scattering asymmetry factor has been estimated. Two different scaling factors to account for dispersion were used. The sensitivity of cloud albedo to spectral dispersion-cloud droplet number concentration relationship in connection to the changes in liquid water content (LWC), and the cloud droplet effective radius has been also investigated. We obtained higher values of effective radius when dispersion is taken into account, with respect to the base case (without considering dispersion). The inferred absolute differences in effective radius values between calculations with each of the scaling factors are below 0.8 {mu}m as LWC ranges between 0.1 and 1.0 g m-3. The optical depth decreased by up to 14% (marine), and up to 29% (continental) when dispersion is considered in both effective radius and asymmetry factor ({beta}LDR scaling factor). Correspondingly, the relative change in cloud albedo is up to 6% (marine) and up to 11% (continental) clouds. For continental clouds, the calculated effective radius when dispersion is considered fits well within the measured range of effective radius in SCAR-B project. The calculated cloud albedo when dispersion is considered shows better agreement with the estimated cloud albedo from measured effective radius in SCAR-B project than the cloud albedo calculated without dispersion. In cleaner

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

    Directory of Open Access Journals (Sweden)

    J. Wang

    2010-08-01

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

  17. Control of aerosol contaminants in indoor air: combining the particle concentration reduction with microbial inactivation.

    Science.gov (United States)

    Grinshpun, Sergey A; Adhikari, Atin; Honda, Takeshi; Kim, Ki Youn; Toivola, Mika; Rao, K S Ramchander; Reponen, Tiina

    2007-01-15

    An indoor air purification technique, which combines unipolar ion emission and photocatalytic oxidation (promoted by a specially designed RCI cell), was investigated in two test chambers, 2.75 m3 and 24.3 m3, using nonbiological and biological challenge aerosols. The reduction in particle concentration was measured size selectively in real-time, and the Air Cleaning Factor and the Clean Air Delivery Rate (CADR) were determined. While testing with virions and bacteria, bioaerosol samples were collected and analyzed, and the microorganism survival rate was determined as a function of exposure time. We observed that the aerosol concentration decreased approximately 10 to approximately 100 times more rapidly when the purifier operated as compared to the natural decay. The data suggest that the tested portable unit operating in approximately 25 m3 non-ventilated room is capable to provide CADR-values more than twice as great than the conventional closed-loop HVAC system with a rating 8 filter. The particle removal occurred due to unipolar ion emission, while the inactivation of viable airborne microorganisms was associated with photocatalytic oxidation. Approximately 90% of initially viable MS2 viruses were inactivated resulting from 10 to 60 min exposure to the photocatalytic oxidation. Approximately 75% of viable B. subtilis spores were inactivated in 10 min, and about 90% or greater after 30 min. The biological and chemical mechanisms that led to the inactivation of stress-resistant airborne viruses and bacterial spores were reviewed.

  18. Investigation of the seasonal variations of aerosol physicochemical properties and their impact on cloud condensation nuclei number concentration

    Science.gov (United States)

    Logan, Timothy S.

    Aerosols are among the most complex yet widely studied components of the atmosphere not only due to the seasonal variability of their physical and chemical properties but also their effects on climate change. The three main aerosol types that are known to affect the physics and chemistry of the atmosphere are: mineral dust, anthropogenic pollution, and biomass burning aerosols. In order to understand how these aerosols affect the atmosphere, this dissertation addresses the following three scientific questions through a combination of surface and satellite observations: SQ1: What are the seasonal and regional variations of aerosol physico-chemical properties at four selected Asian sites? SQ2: How do these aerosol properties change during transpacific and intra-continental long range transport? SQ3: What are the impacts of aerosol properties on marine boundary layer cloud condensation nuclei number concentration? This dissertation uses an innovative approach to classify aerosol properties by region and season to address SQ1. This is useful because this method provides an additional dimension when investigating the physico-chemical properties of aerosols by linking a regional and seasonal dependence to both the aerosol direct and indirect effects. This method involves isolating the aerosol physico-chemical properties into four separate regions using AERONET retrieved Angstrom exponent (AEAOD) and single scattering co-albedo (o oabs) to denote aerosol size and absorptive properties. The aerosols events are then clustered by season. The method is first applied to four AERONET sites representing single mode aerosol dominant regions: weakly absorbing pollution (NASA Goddard), strongly absorbing pollution (Mexico City), mineral dust (Solar Village), and biomass burning smoke (Alta Floresta). The method is then applied to four Asian sites that represent complicated aerosol components. There are strong regional and seasonal influences of the four aerosol types over the

  19. Size-resolved and bulk activation properties of aerosols in the North China plain: the importance of aerosol size distribution in the prediction of CCN number concentration

    Directory of Open Access Journals (Sweden)

    Z. Z. Deng

    2011-01-01

    Full Text Available Size-resolved and bulk activation properties of aerosols were measured at a regional/suburban site in the North China Plain (NCP, which is occasionally heavily polluted by anthropogenic aerosol particles and gases. A CCN (Cloud Condensation Nuclei closure study is conducted with bulk CCN number concentration (NCCN and calculated NCCN based on the aerosol number size distribution and size-resolved activation properties.

    The observed NCCN are higher than those observed in other locations than China, with average NCCN of roughly 2000, 3000, 6000, 10 000 and 13 000 cm−3 at supersaturations of 0.056, 0.083, 0.17, 0.35 and 0.70%, respectively. An inferred critical dry diameter (Dm is calculated based on the measured NCCN and aerosol number size distribution assuming homogeneous chemical composition. This inferred cut off diameter varies in a wide range, indicating that it is impossible to predict NCCN with a fixed critical diameter.

    Size-resolved activation measurements show that most of the 300 nm particles are activated at the investigated supersaturations, while almost no particles of 30 nm are activated even at the highest supersaturation of 0.72%. The activation ratio increases with increasing supersaturation and particle size. The slopes of the activation curves for ambient aerosols are not as steep as those observed in calibrations with ammonium sulfate suggesting that the observed aerosols is an external mixture of more hygroscopic and hydrophobic particles. This conclusion is confirmed by hygroscopicity measurements performed during two intensive field studies in 2009.

    The calculated NCCN based on the size-resolved activation ratio and aerosol number size distribution correlate well with the measured NCCN, and show an average overestimation

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

    Science.gov (United States)

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

    2013-12-17

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

  1. Simulations of organic aerosol concentrations in Mexico City using the WRF-CHEM model during the MCMA-2006/MILAGRO campaign

    Directory of Open Access Journals (Sweden)

    G. Li

    2010-12-01

    Full Text Available Organic aerosol concentrations are simulated using the WRF-CHEM model in Mexico City during the period from 24 to 29 March in association with the MILAGRO-2006 campaign. Two approaches are employed to predict the variation and spatial distribution of the organic aerosol concentrations: (1 a traditional 2-product secondary organic aerosol (SOA model with non-volatile primary organic aerosols (POA; (2 a non-traditional SOA model including the volatility basis-set modeling method in which primary organic components are assumed to be semi-volatile and photochemically reactive and are distributed in logarithmically spaced volatility bins. The MCMA 2006 official emission inventory is used in simulations and the POA emissions are modified and distributed by volatility based on dilution experiments for the non-traditional SOA model. The model results are compared to the Aerosol Mass Spectrometry (AMS observations analyzed using the Positive Matrix Factorization (PMF technique at an urban background site (T0 and a suburban background site (T1 in Mexico City. The traditional SOA model frequently underestimates the observed POA concentrations during rush hours and overestimates the observations in the rest of the time in the city. The model also substantially underestimates the observed SOA concentrations, particularly during daytime, and only produces 21% and 25% of the observed SOA mass in the suburban and urban area, respectively. The non-traditional SOA model performs well in simulating the POA variation, but still overestimates during daytime in the urban area. The SOA simulations are significantly improved in the non-traditional SOA model compared to the traditional SOA model and the SOA production is increased by more than 100% in the city. However, the underestimation during daytime is still salient in the urban area and the non-traditional model also fails to reproduce the high level of SOA concentrations in the suburban area. In the non

  2. Simulations of organic aerosol concentrations in Mexico City using the WRF-CHEM model during the MCMA-2006/MILAGRO campaign

    Directory of Open Access Journals (Sweden)

    G. Li

    2011-04-01

    Full Text Available Organic aerosol concentrations are simulated using the WRF-CHEM model in Mexico City during the period from 24 to 29 March in association with the MILAGRO-2006 campaign. Two approaches are employed to predict the variation and spatial distribution of the organic aerosol concentrations: (1 a traditional 2-product secondary organic aerosol (SOA model with non-volatile primary organic aerosols (POA; (2 a non-traditional SOA model including the volatility basis-set modeling method in which primary organic components are assumed to be semi-volatile and photochemically reactive and are distributed in logarithmically spaced volatility bins. The MCMA (Mexico City Metropolitan Area 2006 official emission inventory is used in simulations and the POA emissions are modified and distributed by volatility based on dilution experiments for the non-traditional SOA model. The model results are compared to the Aerosol Mass Spectrometry (AMS observations analyzed using the Positive Matrix Factorization (PMF technique at an urban background site (T0 and a suburban background site (T1 in Mexico City. The traditional SOA model frequently underestimates the observed POA concentrations during rush hours and overestimates the observations in the rest of the time in the city. The model also substantially underestimates the observed SOA concentrations, particularly during daytime, and only produces 21% and 25% of the observed SOA mass in the suburban and urban area, respectively. The non-traditional SOA model performs well in simulating the POA variation, but still overestimates during daytime in the urban area. The SOA simulations are significantly improved in the non-traditional SOA model compared to the traditional SOA model and the SOA production is increased by more than 100% in the city. However, the underestimation during daytime is still salient in the urban area and the non-traditional model also fails to reproduce the high level of SOA concentrations in the

  3. Intercomparison of elemental concentrations in total and size-fractionated aerosol samples collected during the mace head experiment, April 1991

    Science.gov (United States)

    François, Filip; Maenhaut, Willy; Colin, Jean-Louis; Losno, Remi; Schulz, Michael; Stahlschmidt, Thomas; Spokes, Lucinda; Jickells, Timothy

    During an intercomparison field experiment, organized at the Atlantic coast station of Mace Head, Ireland, in April 1991, aerosol samples were collected by four research groups. A variety of samplers was used, combining both high- and low-volume devices, with different types of collection substrates: Hi-Vol Whatman 41 filter holders, single Nuclepore filters and stacked filter units, as well as PIXE cascade impactors. The samples were analyzed by each participating group, using in-house analytical techniques and procedures. The intercomparison of the daily concentrations for 15 elements, measured by two or more participants, revealed a good agreement for the low-volume samplers for the majority of the elements, but also indicated some specific analytical problems, owing to the very low concentrations of the non-sea-salt elements at the sampling site. With the Hi-Vol Whatman 41 filter sampler, on the other hand, much higher results were obtained in particular for the sea-salt and crustal elements. The discrepancy was dependent upon the wind speed and was attributed to a higher collection efficiency of the Hi-Vol sampler for the very coarse particles, as compared to the low-volume devices under high wind speed conditions. The elemental mass size distribution, as derived from parallel cascade impactor samplings by two groups, showed discrepancies in the submicrometer aerosol fraction, which were tentatively attributed to differences in stage cut-off diameters and/or to bounce-off or splintering effects on the quartz impactor slides used by one of the groups. However, the atmospheric concentrations (sums over all stages) were rather similar in the parallel impactor samples and were only slightly lower than those derived from stacked filter unit samples taken in parallel.

  4. Asian industrial lead inputs to the North Pacific evidenced by lead concentrations and isotopic compositions in surface waters and aerosols.

    Science.gov (United States)

    Gallon, Céline; Ranville, Mara A; Conaway, Christopher H; Landing, William M; Buck, Clifton S; Morton, Peter L; Flegal, A Russell

    2011-12-01

    Recent trends of atmospheric lead deposition to the North Pacific were investigated with analyses of lead in aerosols and surface waters collected on the fourth Intergovernmental Oceanographic Commission Contaminant Baseline Survey from May to June, 2002. Lead concentrations of the aerosols varied by 2 orders of magnitude (0.1-26.4 pmol/m(3)) due in part to variations in dust deposition during the cruise. The ranges in lead aerosol enrichment factors relative to iron (1-119) and aluminum (3-168) were similar, evidencing the transport of Asian industrial lead aerosols across the North Pacific. The oceanic deposition of some of those aerosols was substantiated by the gradient of lead concentrations of North Pacific waters, which varied 3-fold (32.7-103.5 pmol/kg), were highest along with the Asian margin of the basin, and decreased eastward. The hypothesized predominance of Asian industrial lead inputs to the North Pacific was further corroborated by the lead isotopic composition of ocean surface waters ((206)Pb/(207)Pb = 1.157-1.169; (208)Pb/(206)Pb = 2.093-2.118), which fell within the range of isotopic ratios reported in Asian aerosols that are primarily attributed to Chinese industrial lead emissions.

  5. Source apportionment of elevated BaP concentrations in PM10 aerosols in an alpine valley in Austria

    Science.gov (United States)

    Bauer, Heidi; Puxbaum, Hans; Jankowski, Nicole; Sampaio Cordeiro Wagner, Lylian

    2010-05-01

    INTRODUCTION: In a village situated at 1215 m a.s.l. in a natural preserve in an Austrian alpine valley elevated BaP concentrations have been measured in the last years. A highly frequented highway leading from Italy to Germany passes near the village. Monthly means of particulate BaP concentrations show a clear seasonal trend with values below 1 ng/m³ during the warmer months and with concentrations up to 9 ng/m³ in the cold season. Annual averages in the years 2000 - 2005 ranged between 1.4 and 2.8 ng/m³ - much higher than the EU target value of 1 ng/m³. We used a macrotracer model developed at the Vienna University of Technology to determine the contributions of the sources for BaP emissions, which were mainly space heating with wood and traffic from the highway. EXPERIMENTAL: The macrotracer concept is a nine component model to derive source contribution and explains 80-100% of PM10 aerosols in Austria. The amount of traffic exhaust is derived by using EC as tracer, whereas EC produced by wood burning is subtracted, the amount of wood smoke is derived by the anhydro-sugar levoglucosan and the ratio between the anhydro-sugars levoglucosan and mannosan. For the source apportionment of BaP the applied factors reflect on the one hand the composition of the automotive fleet in Austria and on the other hand the composition of the fire wood in the region. Filter samples collected with a high volume sampler in winter were analyzed for PM10 aerosol mass, total, organic, elemental and carbonate carbon, HULIS, anhydro-sugars, polyols and ions (major ions and organic acids) and PAHs. In the same way emission samples taken at a motor test stand and at a test stand for wood combustion were analyzed (Schmidl et al. 2008). The saccharides were determined using high pH anion exchange and pulsed amperometry (HPAE-PAD). Details of the analytical method are given in Iinuma et al., 2009. Elemental and organic carbon were determined with a thermal-optical instrument (Sunset lab

  6. Measurements of CCN-concentrations in the European alpine aerosol using a newly developed static thermal diffusion counter

    Science.gov (United States)

    Hitzenberger, R.; Giebl, H.; Berner, A.; Kromp, R.; Reischl, G.; Kasper-Giebl, A.; Puxbaum, H.

    2000-08-01

    The CCN counter developed at the University of Vienna operates on the principle of a static thermal diffusion chamber. Since 1997, it was used to obtain CCN concentrations in the European alpine background aerosol during intensive measurement campaigns. The 1997 campaign was performed on Mt. Sonnblick (3104 m a.s.l.), while in 1999 and 2000, intensive campaigns were performed on Mt. Rax (1644 m a.s.l.). CCN concentrations at 0.5% supersaturation were found to be comparable ar both sites and also comparable to earlier measurements performed with a commercial CCN counter (DH Associates) on Mt. Sonnblick. Simultaneous measurements of CCN concentration, aerosol number size distribution (measured with a differential mobility particle spectrometer) and cloud liquid water content provided insights into the aerosol/cloud dynamics on Mt. Rax

  7. Evaluating the Role of Boundary Layer Processes on Diurnal Aerosol Concentrations in the Blue Ridge Mountains of Virginia

    Science.gov (United States)

    Lee, T. R.; de Wekker, S.

    2009-12-01

    Forecasting air quality in mountainous terrain is a challenging topic. In this study, we aim to understand the diurnal variability of particulate matter, CO, and CO2 in the Shenandoah National Park (SNP) located in the Blue Ridge Mountains of Virginia. We focus on the effect of atmospheric boundary layer (ABL) dynamics on the diurnal aerosol variability using a combination of observations and numerical modeling. Boundary layer dynamics in mountainous terrain is complicated by a variety of factors such as terrain-induced wind flows. These flows can have a significant impact on atmospheric chemistry but are not well resolved in current air quality forecasting models. In this research, we seek to 1) measure and simulate the diurnal evolution of the ABL at a mountaintop site in the Blue Ridge Mountains, 2) investigate the effect of ABL dynamics on aerosol and CO concentrations on clear days, and 3) investigate the transport of aerosols and pollutants by local, regional, and synoptic-scale flows to the mountaintop using the FLEXPART particle dispersion model and WRF-CHEM model. WRF-CHEM will be run with and without chemistry to isolate the effects of boundary layer dynamics and aerosol formation on diurnal aerosol variability. The results of this study will be incorporated into a diagnostic air quality forecast model for SNP. Measurements come from a 17-m walkup tower that was established in May 2008 along a ridgeline at an elevation of 1037m (38.61°N, 78.35°W) at Pinnacles in the north-central section of SNP. The tower is outfitted with a suite of instruments, including temperature/humidity sensors, cup and sonic anemometers, radiation sensors, a closed-path CO/CO2 gas analyzer, and particle counter. Also, a portable eye-safe LIDAR system is located on-site. In addition, ozone data are collected at a site located nearby. Preliminary results from select clear days in fall, 2008 indicate that ABL height is an important factor governing CO and CO2 concentrations at

  8. Warming-induced increase in aerosol number concentration likely to moderate climate change

    OpenAIRE

    Paasonen, Pauli; Asmi, Ari; Petäjä, Tuukka; Kajos, Maija K.; Äijälä, Mikko

    2013-01-01

    Atmospheric aerosol particles influence the climate system directly by scattering and absorbing solar radiation, and indirectly by acting as cloud condensation nuclei1, 2, 3, 4. Apart from black carbon aerosol, aerosols cause a negative radiative forcing at the top of the atmosphere and substantially mitigate the warming caused by greenhouse gases1. In the future, tightening of controls on anthropogenic aerosol and precursor vapour emissions to achieve higher air quality may weaken this benef...

  9. Leaks in nuclear grade high efficiency aerosol filters

    Energy Technology Data Exchange (ETDEWEB)

    Scripsick, Ronald Clyde [Univ. of California, Davis, CA (United States)

    1994-07-01

    Nuclear grade high efficiency aerosol filters, also known as high efficiency particulate air (HEPA) filters, are commonly used in air cleaning systems for removal of hazardous aerosols. Performance of the filter units is important in assuring health and environmental protection. The filter units are constructed from pleated packs of fiberglass filter media sealed into rigid frames. Results of previous studies on such filter units indicate that their performance may not be completely predicted by ideal performance of the fibrous filter media. In this study, departure from ideal performance is linked to leaks existing in filter units and overall filter unit performance is derived from independent performance of the individual filter unit components. The performance of 14 nuclear grade HEPA filter units (size 1, 25 cfm) with plywood frames was evaluated with a test system that permitted independent determination of penetration as a function of particle size for the whole filter unit, the filter unit frame, and the filter media pack. Tests were performed using a polydisperse aerosol of di-2-ethylhexyl phthalate with a count median diameter of 0.2 {mu}m and geometric standard deviation of 1.6. Flow rate and differential pressure were controlled from 1% to 100% of design values. Particle counts were made upstream and downstream of the filter unit with an optical particle counter (OPC). The OPC provided count information in 28 size channels over the particle diameter range from 0.1 to 0.7 μm. Results provide evidence for a two component leak model of filler unit performance with: (1) external leaks through filter unit frames, and (2) internal leaks through defects in the media and through the seal between the media pack and frame. For the filter units evaluated, these leaks dominate overall filter unit performance over much of the flow rate and particle size ranges tested.

  10. Aerosol formation from high-velocity uranium drops: Comparison of number and mass distributions. Final report

    Energy Technology Data Exchange (ETDEWEB)

    Rader, D.J.; Benson, D.A.

    1995-05-01

    This report presents the results of an experimental study of the aerosol produced by the combustion of high-velocity molten-uranium droplets produced by the simultaneous heating and electromagnetic launch of uranium wires. These tests are intended to simulate the reduction of high-velocity fragments into aerosol in high-explosive detonations or reactor accidents involving nuclear materials. As reported earlier, the resulting aerosol consists mainly of web-like chain agglomerates. A condensation nucleus counter was used to investigate the decay of the total particle concentration due to coagulation and losses. Number size distributions based on mobility equivalent diameter obtained soon after launch with a Differential Mobility Particle Sizer showed lognormal distributions with an initial count median diameter (CMD) of 0.3 {mu}m and a geometric standard deviation, {sigma}{sub g} of about 2; the CMD was found to increase and {sigma}{sub g} decrease with time due to coagulation. Mass size distributions based on aerodynamic diameter were obtained for the first time with a Microorifice Uniform Deposit Impactor, which showed lognormal distributions with mass median aerodynamic diameters of about 0.5 {mu}m and an aerodynamic geometric standard deviation of about 2. Approximate methods for converting between number and mass distributions and between mobility and aerodynamic equivalent diameters are presented.

  11. Warming-induced increase in aerosol number concentration likely to moderate climate change

    NARCIS (Netherlands)

    Paasonen, P.; Asmi, A.; Petäjä, T.; Kajos, M.K.; Äijälä, M.; Junninen, H.; Holst, T.; Abbatt, J.P.D.; Arneth, A.; Birmili, W.; Denier van der Gon, H.A.C.; Hamed, A.; Hoffer, A.; Laakso, L.; Laaksonen, A.; Richard Leaitch, W.; Plass-Dülmer, C.; Pryor, S.C.; Räisänen, P.; Swietlicki, E.; Wiedensohler, A.; Worsnop, D.R.; Kerminen, V.-M.; Kulmala, M.

    2013-01-01

    Atmospheric aerosol particles influence the climate system directly by scattering and absorbing solar radiation, and indirectly by acting as cloud condensation nuclei. Apart from black carbon aerosol, aerosols cause a negative radiative forcing at the top of the atmosphere and substantially mitigate

  12. Chemical composition, sources, and processes of urban aerosols during summertime in Northwest China: insights from High Resolution Aerosol Mass Spectrometry

    Directory of Open Access Journals (Sweden)

    J. Xu

    2014-06-01

    Full Text Available An aerodyne High Resolution Time-of-Flight Aerosol Mass Spectrometer (HR-ToF-AMS was deployed along with a Scanning Mobility Particle Sizer (SMPS and a Multi Angle Absorption Photometers (MAAP to measure the temporal variations of the mass loading, chemical composition, and size distribution of sub-micrometer particulate matter (PM1 in Lanzhou, northwest China, during 12 July–7 August 2012. The average PM1 mass concentration including non-refractory PM1 (NR-PM1 measured by HR-ToF-AMS and black carbon (BC measured by MAAP during this study was 24.5 μg m−3 (ranging from 0.86 to 105μg m−3, with a mean composition consisting of 47% organics, 16% sulfate, 12% BC, 11% ammonium, 10% nitrate, and 4% chloride. The organics was consisted of 70% carbon, 21% oxygen, 8% hydrogen, and 1% nitrogen, with the average oxygen-to-carbon ratio (O / C of 0.33 and organic mass-to-carbon ratio (OM / OC of 1.58. Positive matrix factorization (PMF of the high-resolution mass spectra of organic aerosols (OA identified four distinct factors which represent, respectively, two primary OA (POA emission sources (traffic and food cooking and two secondary OA (SOA types – a fresher, semi-volatile oxygenated OA (SV-OOA and a more aged, low-volatility oxygenated OA (LV-OOA. Traffic-related hydrocarbon-like OA (HOA and BC displayed distinct diurnal patterns both with peak at ~07:00–11:00 (BJT: UTC +8 corresponding to the morning rush hours, while cooking OA (COA peaked during three meal periods. The diurnal profiles of sulfate and LV-OOA displayed a broad peak between ∼07:00–15:00, while those of nitrate, ammonium, and SV-OOA showed a narrower peak at ~08:00–13:00. The later morning and early afternoon peak in the diurnal profiles of secondary aerosol species was likely caused by mixing down of pollutants aloft, which were likely produced in the residual layer decoupled from the boundary layer during night time. The mass spectrum of SV-OOA also showed similarity

  13. Sensitive Detection and Identification of Isovanillin Aerosol Particles at the pg/cm3 Mass Concentration Level using Raman Spectroscopy

    Science.gov (United States)

    2017-04-24

    Particles at the pg/cm3 Mass Concentration Level Using Raman Spectroscopy* R. L. Aggarwal1, S. Di Cecca, L. W. Farrar, Shabshelowitz, A...and identification of isovanillin (C8H8O3, CAS No. 621‐59‐0; Molecular mass 152.15; Density 1.41) aerosol particles of mass concentration MC of 1.8...optical particle sizer. (iv) Aerosol flow cell, fabricated by the U.S. Army Edgewood Chemical and Biological Center (ECBC), with two

  14. [Airborne Fungal Aerosol Concentration and Distribution Characteristics in Air- Conditioned Wards].

    Science.gov (United States)

    Zhang, Hua-ling; Feng, He-hua; Fang, Zi-liang; Wang, Ben-dong; Li, Dan

    2015-04-01

    The effects of airborne fungus on human health in the hospital environment are related to not only their genera and concentrations, but also their particle sizes and distribution characteristics. Moreover, the mechanisms of aerosols with different particle sizes on human health are different. Fungal samples were obtained in medicine wards of Chongqing using a six-stage sampler. The airborne fungal concentrations, genera and size distributions of all the sampling wards were investigated and identified in detail. Results showed that airborne fungal concentrations were not correlated to the diseases or personnel density, but were related to seasons, temperature, and relative humidity. The size distribution rule had roughly the same for testing wards in winter and summer. The size distributions were not related with diseases and seasons, the percentage of airborne fungal concentrations increased gradually from stage I to stage III, and then decreased dramatically from stage V to stage VI, in general, the size of airborne fungi was a normal distribution. There was no markedly difference for median diameter of airborne fungi which was less 3.19 μm in these wards. There were similar dominant genera in all wards. They were Aspergillus spp, Penicillium spp and Alternaria spp. Therefore, attention should be paid to improve the filtration efficiency of particle size of 1.1-4.7 μm for air conditioning system of wards. It also should be targeted to choose appropriate antibacterial methods and equipment for daily hygiene and air conditioning system operation management.

  15. Contribution of ship traffic to aerosol particle concentrations downwind of a major shipping lane

    DEFF Research Database (Denmark)

    Kivekäs, N.; Massling, Andreas; Grythe, H.

    2014-01-01

    by 790 cm(-3) by number and 0.10 gm(-3) by mass. The corresponding daily average values were 170 cm-3 and 0.023 gm-3, respectively. This means that the ship plumes contributed between 11 and 19% to the particle number concentration and between 9 and 18% to PM0.15 during days when air was arriving over......Particles in the atmosphere are of concern due to their toxic properties and effects on climate. In coastal areas, ship emissions can be a significant anthropogenic source. In this study we investigated the contribution from ship emissions to the total particle number and mass concentrations...... at a remote location. We studied the particle number concentration (12 to 490 nm in diameter), the mass concentration (12 to 150 nm in diameter) and number and volume size distribution of aerosol particles in ship plumes for a period of 4.5 months at Hovsore, a coastal site on the western coast of Jutland...

  16. A miniature system for separating aerosol particles and measuring mass concentrations.

    Science.gov (United States)

    Liang, Dao; Shih, Wen-Pin; Chen, Chuin-Shan; Dai, Chi-An

    2010-01-01

    We designed and fabricated a new sensing system which consists of two virtual impactors and two quartz-crystal microbalance (QCM) sensors for measuring particle mass concentration and size distribution. The virtual impactors utilized different inertial forces of particles in air flow to classify different particle sizes. They were designed to classify particle diameter, d, into three different ranges: d3.20 μm. The QCM sensors were coated with a hydrogel, which was found to be a reliable adhesive for capturing aerosol particles. The QCM sensor coated with hydrogel was used to measure the mass loading of particles by utilizing its characteristic of resonant frequency shift. An integrated system has been demonstrated.

  17. A Miniature System for Separating Aerosol Particles and Measuring Mass Concentrations

    Directory of Open Access Journals (Sweden)

    Dao Liang

    2010-04-01

    Full Text Available We designed and fabricated a new sensing system which consists of two virtual impactors and two quartz-crystal microbalance (QCM sensors for measuring particle mass concentration and size distribution. The virtual impactors utilized different inertial forces of particles in air flow to classify different particle sizes. They were designed to classify particle diameter, d, into three different ranges: d < 2.28 μm, 2.28 μm ≤ d ≤ 3.20 μm, d > 3.20 μm. The QCM sensors were coated with a hydrogel, which was found to be a reliable adhesive for capturing aerosol particles. The QCM sensor coated with hydrogel was used to measure the mass loading of particles by utilizing its characteristic of resonant frequency shift. An integrated system has been demonstrated.

  18. High Black Carbon (BC) Concentrations along Indian National Highways

    Science.gov (United States)

    Kumar, S.; Singh, A. K.; Singh, R. P.

    2015-12-01

    Abstract:Black carbon (BC), the optically absorbing component of carbonaceous aerosol, has direct influence on radiation budget and global warming. Vehicular pollution is one of the main sources for poor air quality and also atmospheric pollution. The number of diesel vehicles has increased on the Indian National Highways during day and night; these vehicles are used for the transport of goods from one city to another city and also used for public transport. A smoke plume from the vehicles is a common feature on the highways. We have made measurements of BC mass concentrations along the Indian National Highways using a potable Aethalometer installed in a moving car. We have carried out measurements along Varanasi to Kanpur (NH-2), Varanasi to Durgapur (NH-2), Varanasi to Singrauli (SH-5A) and Varanasi to Ghazipur (NH-29). We have found high concentration of BC along highways, the average BC mass concentrations vary in the range 20 - 40 µg/m3 and found high BC mass concentrations up to 600 μg/m3. Along the highways high BC concentrations were characteristics of the presence of industrial area, power plants, brick kilns and slow or standing vehicles. The effect of increasing BC concentrations along the National Highways and its impact on the vegetation and human health will be presented. Key Words: Black Carbon; Aethalometer; mass concentration; Indian National Highways.

  19. Airship measurements of aerosol size distributions, cloud droplet spectra, and trace gas concentrations in the marine boundary layers

    Energy Technology Data Exchange (ETDEWEB)

    Frick, G.M.; Hoppel, W.A. (Naval Research Lab., Washington, DC (United States))

    1993-11-01

    The use of an airship as a platform to conduct atmospheric chemistry, aerosol, and cloud microphysical research is described, and results from demonstration flights made off the Oregon coast are presented. The slow speed of the airship makes it an ideal platform to do high-spatial resolution profiling both vertically and horizontally, and to measure large aerosol and cloud droplet distributions without the difficulties caused by high-speed aircraft sampling. A unique set of data obtained during the demonstration flights show the effect that processing marine boundary layer aerosol through stratus clouds has on the aerosol size distribution. Evidence of new particle formation (nucleation of particles) was also observed on about half the days on which flights were made. 11 refs., 9 figs., 1 tab.

  20. Single-particle characterization of the high-Arctic summertime aerosol

    Directory of Open Access Journals (Sweden)

    B. Sierau

    2014-07-01

    Full Text Available Single-particle mass-spectrometric measurements were carried out in the high Arctic north of 80° during summer 2008. The campaign took place onboard the icebreaker Oden and was part of the Arctic Summer Cloud Ocean Study (ASCOS. The instrument deployed was an aerosol time-of-flight mass spectrometer (ATOFMS that provides information on the chemical composition of individual particles and their mixing state in real time. Aerosols were sampled in the marine boundary layer at stations in the open ocean, in the marginal ice zone, and in the pack ice region. The largest fraction of particles detected for subsequent analysis in the size range of the ATOFMS between approximately 200 and 3000 nm in diameter showed mass-spectrometric patterns, indicating an internal mixing state and a biomass burning and/or biofuel source. The majority of these particles were connected to an air mass layer of elevated particle concentration mixed into the surface mixed layer from the upper part of the marine boundary layer. The second largest fraction was represented by sea salt particles. The chemical analysis of the over-ice sea salt aerosol revealed tracer compounds that reflect chemical aging of the particles during their long-range advection from the marginal ice zone, or open waters south thereof prior to detection at the ship. From our findings we conclude that long-range transport of particles is one source of aerosols in the high Arctic. To assess the importance of long-range particle sources for aerosol–cloud interactions over the inner Arctic in comparison to local and regional biogenic primary aerosol sources, the chemical composition of the detected particles was analyzed for indicators of marine biological origin. Only a minor fraction showed chemical signatures of potentially ocean-derived primary particles of that kind. However, a chemical bias in the ATOFMS's detection capabilities observed during ASCOS might suggest the presence of a particle type of

  1. Variations in time and space of trace metal aerosol concentrations in urban areas and their surroundings

    Directory of Open Access Journals (Sweden)

    T. Moreno

    2011-09-01

    Full Text Available Using an unprecedentedly large geochemical database, we compare temporal and spatial variations in inhalable trace metal background concentrations in a major city (Barcelona, Spain and at a nearby mountainous site (Montseny affected by the urban plume. Both sites are contaminated by technogenic metals, with V, Pb, Cu, Zn, Mn, Sn, Bi, Sb and Cd all showing upper continental crust (UCC normalised values >1 in broadly increasing order. The highest metal concentrations usually occur during winter at Barcelona and summer in Montseny. This seasonal difference was especially marked at the remote mountain site in several elements such as Ti and Rare Earth Elements, which recorded campaign maxima, exceeding PM10 concentrations seen in Barcelona. The most common metals were Zn, Ti, Cu, Mn, Pb and V. Both V and Ni show highest concentrations in summer, and preferentially fractionate into the finest PM sizes (PM1/PM10 > 0.5 especially in Barcelona, this being attributed to regionally dispersed contamination from fuel oil combustion point sources. Within the city, hourly metal concentrations are controlled either by traffic (rush hour double peak for Cu, Sb, Sn, Ba or industrial plumes (morning peak of Ni, Mn, Cr generated outside the city overnight, whereas at Montseny metal concentrations rise during the morning to a single, prolonged afternoon peak as contaminated air transported by the sea breeze moves into the mountains. Our exceptional database, which includes hourly measurements of chemical concentrations, demonstrates in more detail than previous studies the spatial and temporal variability of urban pollution by trace metals in a given city. Technogenic metalliferous aerosols are commonly fine in size and therefore potentially bioavailable, emphasising the case for basing urban background PM characterisation not only on physical parameters such as mass but also on sample chemistry and with special emphasis on trace

  2. Variations in time and space of trace metal aerosol concentrations in urban areas and their surroundings

    Directory of Open Access Journals (Sweden)

    T. Moreno

    2011-05-01

    Full Text Available Using an unprecedentedly large geochemical database, we compare temporal and spatial variations in inhalable trace metal background concentrations in a major city (Barcelona, Spain and at a nearby mountainous site (Montseny affected by the urban plume. Both sites are contaminated by technogenic metals, with V, Pb, Cu, Zn, Mn, Sn, Bi, Sb and Cd all showing upper continental crust (UCC normalised values >1 in broadly increasing order. The highest metal concentrations usually occur during winter at Barcelona and summer in Montseny. This seasonal difference was especially marked at the remote mountain site in several elements such as Ti and Rare Earth Elements, which recorded campaign maxima, exceeding PM10 concentrations seen in Barcelona. The most common metals were Zn, Ti, Cu, Mn, Pb and V. Both V and Ni show highest concentrations in summer, and preferentially fractionate into the finest PM sizes (PM1/PM10 > 0.5 especially in Barcelona, this being attributed to regionally dispersed contamination from fuel oil combustion point sources. Within the city, hourly metal concentrations are controlled either by traffic (rush hour double peak for Cu, Sb, Sn, Ba or industrial plumes (morning peak of Ni, Mn, Cr generated outside the city overnight, whereas at Montseny metal concentrations rise during the morning to a single, prolonged afternoon peak as contaminated air transported by the sea breeze moves into the mountains. Our exceptional database, which includes hourly measurements of chemical concentrations, demonstrates in more detail than previous studies the spatial and temporal variability of urban pollution by trace metals in a given city. Technogenic metalliferous aerosols are commonly fine in size and therefore potentially bioavailable, emphasising the case for basing urban background PM characterisation not only on physical parameters such as mass but also on sample chemistry and with special emphasis on trace

  3. Highly-controlled, reproducible measurements of aerosol emissions from African biomass combustion

    Science.gov (United States)

    Haslett, Sophie; Thomas, J. Chris; Morgan, William; Hadden, Rory; Liu, Dantong; Allan, James; Williams, Paul; Sekou, Keïta; Liousse, Catherine; Coe, Hugh

    2017-04-01

    Particulate emissions from biomass burning can alter the atmosphere's radiative balance and cause significant harm to human health. However, the relationship between these emissions and fundamental combustion processes is, to date, poorly characterised. In atmospheric models, aerosol emissions are represented by emission factors based on mass loss, which are averaged over an entire combustion event for each particulate species. This approach, however, masks huge variability in emissions during different phases of the combustion period. Laboratory tests have shown that even small changes to the burning environment can lead to huge variation in observed aerosol emission factors (Akagi et al., 2011). In order to address this gap in understanding, in this study, small wood samples sourced from Côte D'Ivoire were burned in a highly-controlled laboratory environment. The shape and mass of samples, available airflow and surrounding heat were carefully regulated. Organic aerosol and refractory black carbon emissions were measured in real-time using an Aerosol Mass Spectrometer and a Single Particle Soot Photometer, respectively. Both of these instruments are used regularly to measure aerosol concentrations in the field. This methodology produced remarkably repeatable results, allowing three different phases of combustion to be identified by their emissions. Black carbon was emitted predominantly during flaming combustion; organic aerosols were emitted during pyrolysis before ignition and from smouldering-dominated behaviour near the end of combustion. During the flaming period, there was a strong correlation between the emission of black carbon and the rate of mass loss, which suggests there is value in employing a mass-based emission factor for this species. However, very little correlation was seen between organic aerosol and mass loss throughout the tests. As such, results here suggest that emission factors averaged over an entire combustion event are unlikely to be

  4. The electrical charging of inactive aerosols in high ionised atmosphere, the electrical charging of artificial beta radioactive aerosols; Le processus de charge electrique: des aerosols non radioactifs en milieu fortement ionise, des aerosols radioactifs artificiels emetteurs beta

    Energy Technology Data Exchange (ETDEWEB)

    Gensdarmes, F

    2000-07-01

    The electrical properties of aerosols greatly influence their transport and deposition in a containment. In a bipolar ionic atmosphere, a neutral electric charge on aerosols is commonly assumed. However, many studies report a different charge distribution in some situations, like highly ionised atmosphere or in the case of radioactive aerosols. Such situations could arise from a hypothetical accident in a nuclear power plant. Within the framework of safety studies which are carried out at IPSN, our aims were the study of electrical properties of aerosols in highly ionised atmosphere, and the study of artificial radioactive aerosols, in order to suggest experimental validation of available theories. For this purpose, we designed an experimental device that allows us to measure non-radioactive aerosol charge distribution under high gamma irradiation, up to 10{sup 4} Gy/h. With our experimental device we also studied the properties of small ions in the medium. Our results show a variation of the charge distribution in highly ionised atmosphere. The charge increases with the dose of gamma ray. We have related this variation with the one of the small ions in the gases, according to theoretical prediction. However, the model overestimates slightly our experimental results. In the case of the radioactive aerosols, we have designed an original experimental device, which allows us to study the charge distribution of a {sup 137}Cs aerosol. Our results show that the electric charging of such aerosols is strongly dependent on evolution parameters in a containment. So, our results underline a great enhancement of self-charging of particles which are sampled in a confined medium. Our results are qualitatively in agreement with the theoretical model; nevertheless the latter underestimates appreciably the self-charging, owing to the fact that wall effects are not taken into account. (author)

  5. Characterizing the influence of anthropogenic emissions and transport variability on sulfate aerosol concentrations at Mauna Loa Observatory

    Science.gov (United States)

    Potter, Lauren E.

    Sulfate aerosol in the atmosphere has substantial impacts on human health and environmental quality. Most notably, atmospheric sulfate has the potential to modify the earth's climate system through both direct and indirect radiative forcing mechanisms (Meehl et al., 2007). Emissions of sulfur dioxide, the primary precursor of sulfate aerosol, are now globally dominated by anthropogenic sources as a result of widespread fossil fuel combustion. Economic development in Asian countries since 1990 has contributed considerably to atmospheric sulfur loading, particularly China, which currently emits approximately 1/3 of global anthropogenic SO2 (Klimont et al., 2013). Observational and modeling studies have confirmed that anthropogenic pollutants from Asian sources can be transported long distances with important implications for future air quality and global climate change. Located in the remote Pacific Ocean (19.54°N, 155.58°W) at an elevation of 3.4 kilometers above sea level, Mauna Loa Observatory (MLO) is an ideal measurement site for ground-based, free tropospheric observations and is well situated to experience influence from springtime Asian outflow. This study makes use of a 14-year data set of aerosol ionic composition, obtained at MLO by the University of Hawaii at Manoa. Daily filter samples of total aerosol concentrations were made during nighttime downslope (free-tropospheric) transport conditions, from 1995 to 2008, and were analyzed for aerosol-phase concentrations of the following species: nitrate (NO3-), sulfate (SO42-), methanesulfonate (MSA), chloride (Cl-), oxalate, sodium (Na+), ammonium (NH 4+), potassium (K+), magnesium (Mg 2+), and calcium (Ca2+). An understanding of the factors controlling seasonal and interannual variations in aerosol speciation and concentrations at this site is complicated by the relatively short lifetimes of aerosols, compared with greenhouse gases which have also been sampled over long time periods at MLO. Aerosol filter

  6. Hourly elemental concentrations in PM2.5 aerosols sampled simultaneously at urban background and road site during SAPUSS - diurnal variations and PMF receptor modelling

    Science.gov (United States)

    Dall'Osto, M.; Querol, X.; Amato, F.; Karanasiou, A.; Lucarelli, F.; Nava, S.; Calzolai, G.; Chiari, M.

    2013-04-01

    Hourly-resolved aerosol chemical speciation data can be a highly powerful tool to determine the source origin of atmospheric pollutants in urban environments. Aerosol mass concentrations of seventeen elements (Na, Mg, Al, S, Cl, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Sr and Pb) were obtained by time (1 h) and size (PM2.5 particulate matter < 2.5 μm) resolved aerosol samples analysed by Particle Induced X-ray Emission (PIXE) measurements. In the Marie Curie European Union framework of SAPUSS (Solving Aerosol Problems by Using Synergistic Strategies), the approach used is the simultaneous sampling at two monitoring sites in Barcelona (Spain) during September-October 2010: an urban background site (UB) and a street canyon traffic road site (RS). Elements related to primary non-exhaust traffic emission (Fe, Cu), dust resuspension (Ca) and anthropogenic Cl were found enhanced at the RS, whereas industrial related trace metals (Zn, Pb, Mn) were found at higher concentrations at the more ventilated UB site. When receptor modelling was performed with positive matrix factorization (PMF), nine different aerosol sources were identified at both sites: three types of regional aerosols (regional sulphate (S) - 27%, biomass burning (K) - 5%, sea salt (Na-Mg) - 17%), three types of dust aerosols (soil dust (Al-Ti) - 17%, urban crustal dust (Ca) - 6%, and primary traffic non-exhaust brake dust (Fe-Cu) - 7%), and three types of industrial aerosol plumes-like events (shipping oil combustion (V-Ni) - 17%, industrial smelters (Zn-Mn) - 3%, and industrial combustion (Pb-Cl) - 5%, percentages presented are average source contributions to the total elemental mass measured). The validity of the PMF solution of the PIXE data is supported by very good correlations with external single particle mass spectrometry measurements. Some important conclusions can be drawn about the PM2.5 mass fraction simultaneously measured at the UB and RS sites: (1) the regional aerosol sources impact both

  7. Importance of aerosol composition and mixing state for cloud droplet activation in the high Arctic

    Directory of Open Access Journals (Sweden)

    C. Leck

    2014-08-01

    Full Text Available Concentrations of cloud condensation nuclei (CCN were measured throughout an expedition by icebreaker around the central Arctic Ocean, including a 3 week ice drift operation at 87° N, from 3 August to 9 September 2008. In agreement with previous observations in the area and season median daily CCN concentrations at 0.2% water vapor supersaturation were typically in the range of 15 to 30 cm−3, but concentrations varied by two to three orders of magnitude over the expedition and were occasionally below 1 cm−3. The CCN concentrations were highest near the ice edge and fell by a factor of three in the first 48 h of transport from the open sea into the pack ice region. For longer transport times they increased again indicating a local source over the pack ice, suggested to be polymer gels, via drops injected into the air by bubbles bursting on open leads. By assuming Köhler theory and simulating the cloud nucleation process using a Lagrangian adiabatic air parcel model that solves the kinetic formulation for condensation of water on size resolved aerosol particles we inferred the properties of the unexplained non-water soluble aerosol fraction that is necessary for reproducing the observed concentrations of CCN. We propose that the portion of the internally/externally mixed water insoluble particles was larger in the corresponding smaller aerosol sizes ranges. These particles were physically and chemically behaving as polymer gels: the interaction of the hydrophilic and hydrophobic entities on the structures of polymer gels during cloud droplet activation would at first only show a partial wetting character and only weak hygroscopic growth. Given time, a high CCN activation efficiency is achieved, which is promoted by the hydrophilicity or surface-active properties of the gels. Thus the result in this study argues for that the behavior of the high Arctic aerosol in CCN-counters operating at water vapor supersaturations > 0.4% (high relative

  8. Sensitivity of aerosol concentrations and cloud properties to nucleation and secondary organic distribution in ECHAM5-HAM global circulation model

    Directory of Open Access Journals (Sweden)

    R. Makkonen

    2008-06-01

    Full Text Available The global aerosol-climate model ECHAM5-HAM was modified to improve the representation of new particle formation in the boundary layer. Activation-type nucleation mechanism was introduced to produce observed nucleation rates in lower troposphere. A simple and computationally efficient model for biogenic secondary organic aerosol (BSOA formation was implemented. We studied the sensitivity of aerosol and cloud droplet number concentrations (CDNC to these additions. Activation-type nucleation significantly increases aerosol number concentrations in the boundary layer. Increased particle number concentrations have a significant effect also on cloud droplet number concentrations and therefore on cloud properties. We performed calculations with activation nucleation coefficient values of 2×10-7 s−1, 2×10-6 s-1 and 2×10-5 s−1 to evaluate the sensitivity to this parameter. For BSOA we have used yields of 0.025, 0.07 and 0.15 to estimate the amount of monoterpene oxidation products available for condensation. The dynamic SOA scheme induces large regional changes to size distribution of organic carbon, and therefore affects particle optical properties and cloud droplet number concentrations locally. Comparison with satellite observation shows that activation-type nucleation significantly decreases the differences between observed and modeled values of cloud top CDNC.

  9. Daily and seasonal variation of aerosol concentration in the atmosphere near the surface in continental climate of Siberia

    Energy Technology Data Exchange (ETDEWEB)

    Koutsenogii, P. [Inst. of Chemical Kinetics and Combustion, Novosibirsk (Russian Federation)

    1995-12-31

    Novosibirsk region is the area in southern part of West-Siberian lowland, covering about 200,000 km{sup 2}. The properties of atmospheric aerosol in Novosibirsk region were studied during few campaigns in the years 1992 and 1993, one complex expedition in Summer of 1994 and durable observations in Akademgorodok in the years 1993, 1994. Akademgorodok is situated 25 km S from the city Novosibirsk, has population of about 100,000 and no industry. Three different locations in remote areas of Novosibirsk region were used for the measurements. The first was situated 12 km E from Akademgorodok, and 30 km from Novosibirsk near the village Kljutchi. The second location was situated close to Lake Tchany in western part of Novosibirsk region. The third location was situated in south-western part of Novosibirsk region, 12 km from the town Karasuk. The total aerosol light scattering by aerosol particles was measured by commercially available nephelometer FAN-A in terms of units, related to the molecular scattering of clean air, measured by the same nephelometer. Aerosol samples in which the content of sulfate-, nitrate-, and cloride-anions was determined, using ion liquid chromatography, were collected with Whatman 41 or AFA-HA filters. Aerosol mass concentration was measured by weighting of AFA-HA filters. Aerosol particles were sampled on the filters with the volume velocity of about 500 l/min for Whatman 41 and 120 l/min for AFA-HA and mean sampling duration of 24 hours. The total aerosol number concentration was measured with a condensation nuclei counter TSI 3020

  10. Sources and atmospheric processing of winter aerosols in Seoul, Korea: insights from real-time measurements using a high-resolution aerosol mass spectrometer

    Science.gov (United States)

    Kim, Hwajin; Zhang, Qi; Bae, Gwi-Nam; Kim, Jin Young; Bok Lee, Seung

    2017-02-01

    Highly time-resolved chemical characterization of nonrefractory submicrometer particulate matter (NR-PM1) was conducted in Seoul, the capital and largest metropolis of Korea, using an Aerodyne high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS). The measurements were performed during winter, when elevated particulate matter (PM) pollution events are often observed. This is the first time that detailed real-time aerosol measurement results have been reported from Seoul, Korea, and they reveal valuable insights into the sources and atmospheric processes that contribute to PM pollution in this region. The average concentration of submicron aerosol (PM1 = NR-PM1+ black carbon (BC)) was 27.5 µg m-3, and the total mass was dominated by organics (44 %), followed by nitrate (24 %) and sulfate (10 %). The average atomic ratios of oxygen to carbon (O / C), hydrogen to carbon (H / C), and nitrogen to carbon (N / C) of organic aerosols (OA) were 0.37, 1.79, and 0.018, respectively, which result in an average organic mass-to-carbon (OM / OC) ratio of 1.67. The concentrations (2.6-90.7 µg m-3) and composition of PM1 varied dynamically during the measurement period due to the influences of different meteorological conditions, emission sources, and air mass origins. Five distinct sources of OA were identified via positive matrix factorization (PMF) analysis of the HR-ToF-AMS data: vehicle emissions represented by a hydrocarbon-like OA factor (HOA, O / C = 0.06), cooking activities represented by a cooking OA factor (COA, O / C = 0.14), wood combustion represented by a biomass burning OA factor (BBOA, O / C = 0.34), and secondary organic aerosol (SOA) represented by a semivolatile oxygenated OA factor (SV-OOA, O / C = 0.56) and a low-volatility oxygenated OA factor (LV-OOA, O / C = 0.68). On average, primary OA (POA = HOA + COA + BBOA) accounted for 59 % the OA mass, whereas SV-OOA and LV-OOA contributed 15 and 26 %, respectively. Our results indicate that air

  11. The effect of surfactant and solid phase concentration on drug aggregates in model aerosol propellent suspensions.

    Science.gov (United States)

    Bower, C; Washington, C; Purewal, T S

    1996-04-01

    The effect of increasing solid phase concentration on the morphology and flocculation rate of model aerosol suspensions has been investigated. Suspensions of micronized salbutamol sulphate and lactose in trichlorotrifluoroethane (P113) were studied under conditions of increasing shear stress. By use of image analysis techniques, measurement of aggregate size, fractal dimension and rate of aggregation was performed. The effect of the surfactant sorbitan monooleate on morphology and flocculation rate was also studied. Increased solid phase concentration caused an increase in the rate of aggregation and average aggregate size at a given value of shear stress. Surfactant addition retarded the aggregation rate, and caused a shift from a diffusion-limited cluster aggregation to a reaction-limited cluster aggregation mechanism. The aggregate profiles showed a corresponding change from rugged and crenellated without surfactant, to increasingly smooth and Euclidian with increasing surfactant concentration. The morphological changes were characterized by a decrease in the average boundary fractal dimension which also correlated well with the corresponding reduction in aggregation rate.

  12. Explaining global surface aerosol number concentrations in terms of primary emissions and particle formation

    Directory of Open Access Journals (Sweden)

    D. V. Spracklen

    2010-05-01

    Full Text Available We synthesised observations of total particle number (CN concentration from 36 sites around the world. We found that annual mean CN concentrations are typically 300–2000 cm−3 in the marine boundary layer and free troposphere (FT and 1000–10 000 cm−3 in the continental boundary layer (BL. Many sites exhibit pronounced seasonality with summer time concentrations a factor of 2–10 greater than wintertime concentrations. We used these CN observations to evaluate primary and secondary sources of particle number in a global aerosol microphysics model. We found that emissions of primary particles can reasonably reproduce the spatial pattern of observed CN concentration (R2=0.46 but fail to explain the observed seasonal cycle (R2=0.1. The modeled CN concentration in the FT was biased low (normalised mean bias, NMB=−88% unless a secondary source of particles was included, for example from binary homogeneous nucleation of sulfuric acid and water (NMB=−25%. Simulated CN concentrations in the continental BL were also biased low (NMB=−74% unless the number emission of anthropogenic primary particles was increased or a mechanism that results in particle formation in the BL was included. We ran a number of simulations where we included an empirical BL nucleation mechanism either using the activation-type mechanism (nucleation rate, J, proportional to gas-phase sulfuric acid concentration to the power one or kinetic-type mechanism (J proportional to sulfuric acid to the power two with a range of nucleation coefficients. We found that the seasonal CN cycle observed at continental BL sites was better simulated by BL particle formation (R2=0.3 than by increasing the number emission from primary anthropogenic sources (R2=0.18. The nucleation constants that resulted in best overall match between model and observed CN concentrations were

  13. Tropospheric Aerosols

    Science.gov (United States)

    Buseck, P. R.; Schwartz, S. E.

    2003-12-01

    m, PM10=1.1 μg m-3; estimated coefficient of light scattering by particulate matter, σep, at 570 nm=12 Mm-1). (b) High aerosol concentration (PM2.5=43.9 μg m-3; PM10=83.4 μg m-3; estimated σep at 570 nm=245 Mm-1) (reproduced by permission of National Park Service, 2002). Although comprising only a small fraction of the mass of Earth's atmosphere, aerosol particles are highly important constituents of the atmosphere. Special interest has focused on aerosols in the troposphere, the lowest part of the atmosphere, extending from the land or ocean surface typically to ˜8 km at high latitudes, ˜12 km in mid-latitudes, and ˜16 km at low latitudes. That interest arises in large part because of the importance of aerosol particles in geophysical processes, human health impairment through inhalation, environmental effects through deposition, visibility degradation, and influences on atmospheric radiation and climate.Anthropogenic aerosols are thought to exert a substantial influence on Earth's climate, and the need to quantify this influence has sparked much of the current interest in and research on tropospheric aerosols. The principal mechanisms by which aerosols influence the Earth radiation budget are scattering and absorbing solar radiation (the so-called "direct effects") and modifying clouds and precipitation, thereby affecting both radiation and hydrology (the so-called "indirect effects"). Light scattering by aerosols increases the brightness of the planet, producing a cooling influence. Light-absorbing aerosols such as black carbon exert a warming influence. Aerosols increase the reflectivity of clouds, another cooling influence. These radiative influences are quantified as forcings, where a forcing is a perturbation to the energy balance of the atmosphere-Earth system, expressed in units of watts per square meter, W m-2. A warming influence is denoted a positive forcing, and a cooling influence, negative. The radiative direct and indirect forcings by

  14. Airborne High Spectral Resolution Lidar Aerosol Measurements during MILAGRO and TEXAQS/GOMACCS

    Science.gov (United States)

    Ferrare, Richard; Hostetler, Chris; Hair, John; Cook Anthony; Harper, David; Burton, Sharon; Clayton, Marian; Clarke, Antony; Russell, Phil; Redemann, Jens

    2007-01-01

    Two1 field experiments conducted during 2006 provided opportunities to investigate the variability of aerosol properties near cities and the impacts of these aerosols on air quality and radiative transfer. The Megacity Initiative: Local and Global Research Observations (MILAGRO) /Megacity Aerosol Experiment in Mexico City (MAX-MEX)/Intercontinental Chemical Transport Experiment-B (INTEX-B) joint experiment conducted during March 2006 investigated the evolution and transport of pollution from Mexico City. The Texas Air Quality Study (TEXAQS)/Gulf of Mexico Atmospheric Composition and Climate Study (GoMACCS) (http://www.al.noaa.gov/2006/) conducted during August and September 2006 investigated climate and air quality in the Houston/Gulf of Mexico region. During both missions, the new NASA Langley airborne High Spectral Resolution Lidar (HSRL) was deployed on the NASA Langley B200 King Air aircraft and measured profiles of aerosol extinction, backscattering, and depolarization to: 1) characterize the spatial and vertical distributions of aerosols, 2) quantify aerosol extinction and optical thickness contributed by various aerosol types, 3) investigate aerosol variability near clouds, 4) evaluate model simulations of aerosol transport, and 5) assess aerosol optical properties derived from a combination of surface, airborne, and satellite measurements.

  15. Separating mixtures of aerosol types in airborne High Spectral Resolution Lidar data

    Science.gov (United States)

    Burton, S. P.; Vaughan, M. A.; Ferrare, R. A.; Hostetler, C. A.

    2014-02-01

    Knowledge of aerosol type is important for determining the magnitude and assessing the consequences of aerosol radiative forcing, and can provide useful information for source attribution studies. However, atmospheric aerosol is frequently not a single pure type, but instead occurs as a mixture of types, and this mixing affects the optical and radiative properties of the aerosol. This paper extends the work of earlier researchers by using the aerosol intensive parameters measured by the NASA Langley Research Center airborne High Spectral Resolution Lidar (HSRL-1) to develop a comprehensive and unified set of rules for characterizing the external mixing of several key aerosol intensive parameters: extinction-to-backscatter ratio (i.e., lidar ratio), backscatter color ratio, and depolarization ratio. We present the mixing rules in a particularly simple form that leads easily to mixing rules for the covariance matrices that describe aerosol distributions, rather than just single values of measured parameters. These rules can be applied to infer mixing ratios from the lidar-observed aerosol parameters, even for cases without significant depolarization. We demonstrate our technique with measurement curtains from three HSRL-1 flights which exhibit mixing between two aerosol types, urban pollution plus dust, marine plus dust, and smoke plus marine. For these cases, we infer a time-height cross-section of extinction mixing ratio along the flight track, and partition aerosol extinction into portions attributed to the two pure types.

  16. Separating mixtures of aerosol types in airborne High Spectral Resolution Lidar data

    Directory of Open Access Journals (Sweden)

    S. P. Burton

    2013-09-01

    Full Text Available Knowledge of aerosol type is important for source attribution and for determining the magnitude and assessing the consequences of aerosol radiative forcing. However, atmospheric aerosol is frequently not a single pure type, but instead occurs as a mixture of types, and this mixing affects the optical and radiative properties of the aerosol. This paper extends the work of earlier researchers by using the aerosol intensive parameters measured by the NASA Langley Research Center airborne High Spectral Resolution Lidar (HSRL-1 to develop a comprehensive and unified set of rules for characterizing the external mixing of several key aerosol intensive parameters: extinction-to-backscatter ratio (i.e. lidar ratio, backscatter color ratio, and depolarization ratio. We present the mixing rules in a particularly simple form that leads easily to mixing rules for the covariance matrices that describe aerosol distributions, rather than just scalar values of measured parameters. These rules can be applied to infer mixing ratios from the lidar-observed aerosol parameters, even for cases without significant depolarization. We demonstrate our technique with measurement curtains from three HSRL-1 flights which exhibit mixing between two aerosol types, urban pollution plus dust, marine plus dust, and smoke plus marine. For these cases, we infer a time-height cross-section of mixing ratio along the flight track, and partition aerosol extinction into portions attributed to the two pure types.

  17. Interfacing the NRL 1-D High Vertical Resolution Aerosol Model with COAMPS

    Science.gov (United States)

    2016-06-13

    mechanistic model that predicts the evolution of the aerosol size and composition distribution. From such a model, aerosol extinction of EM radiation can be...calculated in a highly structured atmospheric marine boundary layer (AMBL) and used to evaluate and predict the performance of systems that operate...sea-salt AOD ranging from 0.01 - 0.10 (0.05 - 0.10 under moderate winds). IMPACT/APPLICATIONS Aerosols scatter and absorb EM radiation and are

  18. Seasonal changes in Fe species and soluble Fe concentration in the atmosphere in the Northwest Pacific region based on the analysis of aerosols collected in Tsukuba, Japan

    Directory of Open Access Journals (Sweden)

    Y. Takahashi

    2013-08-01

    Full Text Available Atmospheric iron (Fe can be a significant source of nutrition for phytoplankton inhabiting remote oceans, which in turn has a large influence on the Earth's climate. The bioavailability of Fe in aerosols depends mainly on the fraction of soluble Fe (= [FeSol]/[FeTotal], where [FeSol] and [FeTotal] are the atmospheric concentrations of soluble and total Fe, respectively. However, the numerous factors affecting the soluble Fe fraction have not been fully understood. In this study, the Fe species, chemical composition, and soluble Fe concentrations in aerosols collected in Tsukuba, Japan were investigated over a year (nine samples from December 2002 to October 2003 to identify the factors affecting the amount of soluble Fe supplied into the ocean. The soluble Fe concentration in aerosols is correlated with those of sulfate and oxalate originated from anthropogenic sources, suggesting that soluble Fe is mainly derived from anthropogenic sources. Moreover, the soluble Fe concentration is also correlated with the enrichment factors of vanadium and nickel emitted by fossil fuel combustion. These results suggest that the degree of Fe dissolution is influenced by the magnitude of anthropogenic activity, such as fossil fuel combustion. X-ray absorption fine structure (XAFS spectroscopy was performed in order to identify the Fe species in aerosols. Fitting of XAFS spectra coupled with micro X-ray fluorescence analysis (μ-XRF showed the main Fe species in aerosols in Tsukuba to be illite, ferrihydrite, hornblende, and Fe(III sulfate. Moreover, the soluble Fe fraction in each sample measured by leaching experiments is closely correlated with the Fe(III sulfate fraction determined by the XAFS spectrum fitting, suggesting that Fe(III sulfate is the main soluble Fe in the ocean. Another possible factor that can control the amount of soluble Fe supplied into the ocean is the total Fe(III concentration in the atmosphere, which was high in spring due to the high

  19. Seasonal changes in Fe species and soluble Fe concentration in the atmosphere in the Northwest Pacific region based on the analysis of aerosols collected in Tsukuba, Japan

    Directory of Open Access Journals (Sweden)

    Y. Takahashi

    2013-03-01

    Full Text Available Atmospheric iron (Fe can be a significant source of nutrition for phytoplankton inhabiting remote oceans, which in turn has a large influence on the Earth's climate. The bioavailability of Fe in aerosols depends mainly on the fraction of soluble Fe (= [FeSol]/[FeTotal], where [FeSol] and [FeTotal] are the atmospheric concentrations of soluble and total Fe, respectively. However, the numerous factors affecting the soluble Fe fraction have not been fully understood. In this study, the Fe species, chemical composition, and soluble Fe concentrations in aerosols collected in Tsukuba, Japan were investigated over a year (nine samples from December 2002 to October 2003 to identify the factors affecting the amount of soluble Fe supplied into the ocean. The soluble Fe concentration in aerosols is correlated with those of sulfate and oxalate originated from anthropogenic sources, suggesting that soluble Fe is mainly derived from anthropogenic sources. Moreover, the soluble Fe concentration is also correlated with the enrichment factors of vanadium and nickel emitted by fossil fuel combustion. These results suggest that the degree of Fe dissolution is influenced by the magnitude of anthropogenic activity, such as fossil fuel combustion. X-ray absorption fine structure (XAFS spectroscopy was performed in this study to identify the Fe species in aerosols. The fitting of XAFS spectra coupled with micro X-ray fluorescence analysis (XRF determined the main Fe species in aerosols in Tsukuba to be illite, ferrihydrite, hornblende, and Fe(III sulfate. Moreover, the soluble Fe fraction in each sample measured by leaching experiments is closely correlated with the Fe(III sulfate fraction determined by the XAFS spectrum fitting, suggesting that Fe(III sulfate is the main soluble Fe in the ocean. Another possible factor that can control the amount of soluble Fe supplied into the ocean is the total Fe(III concentration in the atmosphere, which was high in spring due to

  20. Aerosol hygroscopicity at high (99 to 100% relative humidities

    Directory of Open Access Journals (Sweden)

    C. R. Ruehl

    2009-07-01

    Full Text Available The hygroscopicity of an aerosol largely determines its influence on climate and, for smaller particles, atmospheric lifetime. While much aerosol hygroscopicity data is available at lower relative humidities (RH and under cloud formation conditions (RH>100%, relatively little data is available at high RH (99.2 to 99.9%. We measured the size of droplets at high RH that had formed on particles composed of one of seven compounds with dry diameters between 0.1 and 0.5 μm, and calculated the hygroscopicity of these compounds. We use a parameterization of the Kelvin term, in addition to a standard parameterization (κ of the Raoult term, to express the hygroscopicity of surface-active compounds.

    For inorganic compounds, hygroscopicity could reliably be predicted using water activity data and assuming a surface tension of pure water. In contrast, most organics exhibited a slight to mild increase in hygroscopicity with droplet diameter. This trend was strongest for sodium dodecyl sulfate (SDS, the most surface-active compound studied. The results suggest that partitioning of surface-active compounds away from the bulk solution, which reduces hygroscopicity, dominates any increases in hygroscopicity due to reduced surface tension. This is opposite to what is typically assumed for soluble surfactants. Furthermore, we saw no evidence that micellization limits SDS activity in micron-sized solution droplets, as observed in macroscopic solutions. These results suggest that while the high-RH hygroscopicity of inorganic compounds can be reliably predicted using readily available data, surface-activity parameters obtained from macroscopic solutions with organic solutes may be inappropriate for calculations of the hygroscopicity of micron-sized droplets.

  1. Determining radioactive aerosol concentrations using a surface radioactive contamination measurement device.

    Science.gov (United States)

    Cerny, R; Johnova, K; Kozlovska, M; Otahal, P; Vosahlikova, I

    2015-06-01

    For experiments with dispersed radioactive aerosols in a radon-aerosol chamber (RAC), it is desirable to know the activity of the radioactive aerosols applied in the RAC. A COLIBRI TTC survey metre with an SABG-15+ probe (Canberra, USA) was purchased for this purpose. The probe is designed for surface contamination measurements, and it is intended to measure the activity of aerosols deposited on the filters during experiments in the RAC. Since the probe is calibrated in a different geometry, its response in the authors' experimental geometry was simulated by a Monte Carlo method. The authors present a Monte Carlo model using MCNPX and an experimental verification of this probe model.

  2. Observations of fluorescent and biological aerosol at a high-altitude site in Central France

    Directory of Open Access Journals (Sweden)

    A. M. Gabey

    2013-01-01

    >
    Analysis of organic mass spectra recorded using an Aerosol Mass Spectrometer (AMS; Aerodyne Inc. suggests that aerosol reaching the site at night was more aged than that during the day, indicative of sampling the residual layer at night. Supplementary meteorological data and previous work also show that pdD lies in the residual layer/free troposphere at night, and this is thought to cause the observed diurnal cycles in organic-type and fluorescent aerosol particles.

    Based on the observed disparity between bacteria and fluorescent particle concentrations, fluorescent non-PBA is likely to be important in the WIBS-3 data and the surprisingly high fluorescent concentration in the residual layer/free troposphere raises questions about a ubiquitous background in continental air during the summer.

  3. Observations of fluorescent and biological aerosol at a high-altitude site in central France

    Science.gov (United States)

    Gabey, A. M.; Vaitilingom, M.; Freney, E.; Boulon, J.; Sellegri, K.; Gallagher, M. W.; Crawford, I. P.; Robinson, N. H.; Stanley, W. R.; Kaye, P. H.

    2013-08-01

    an aerosol mass spectrometer (AMS; Aerodyne Inc.) suggests that aerosol reaching the site at night was more aged than that during the day, indicative of sampling the residual layer at night. Supplementary meteorological data and previous work also show that PdD lies in the residual layer/free troposphere at night, and this is thought to cause the observed diurnal cycles in organic-type and fluorescent aerosol particles. Based on the observed disparity between bacteria and fluorescent particle concentrations, fluorescent non-PBA is likely to be important in the WIBS-3 data and the surprisingly high fluorescent concentration in the residual layer/free troposphere raises questions about a ubiquitous background in continental air during the summer.

  4. The potential of LIRIC to validate the vertical profiles of the aerosol mass concentration estimated by an air quality model

    Science.gov (United States)

    Siomos, Nikolaos; Filoglou, Maria; Poupkou, Anastasia; Liora, Natalia; Dimopoulos, Spyros; Melas, Dimitris; Chaikovsky, Anatoli; Balis, Dimitris

    2015-04-01

    Vertical profiles of the aerosol mass concentration derived by a retrieval algorithm that uses combined sunphotometer and LIDAR data (LIRIC) were used in order to validate the mass concentration profiles estimated by the air quality model CAMx. LIDAR and CIMEL measurements of the Laboratory of Atmospheric Physics of the Aristotle University of Thessaloniki were used for this validation.The aerosol mass concentration profiles of the fine and coarse mode derived by CAMx were compared with the respective profiles derived by the retrieval algorithm. For the coarse mode particles, forecasts of the Saharan dust transportation model BSC-DREAM8bV2 were also taken into account. Each of the retrieval algorithm's profiles were matched to the models' profile with the best agreement within a time window of four hours before and after the central measurement. OPAC, a software than can provide optical properties of aerosol mixtures, was also employed in order to calculate the angstrom exponent and the lidar ratio values for 355nm and 532nm for each of the model's profiles aiming in a comparison with the angstrom exponent and the lidar ratio values derived by the retrieval algorithm for each measurement. The comparisons between the fine mode aerosol concentration profiles resulted in a good agreement between CAMx and the retrieval algorithm, with the vertical mean bias error never exceeding 7 μgr/m3. Concerning the aerosol coarse mode concentration profiles both CAMx and BSC-DREAM8bV2 values are severely underestimated, although, in cases of Saharan dust transportation events there is an agreement between the profiles of BSC-DREAM8bV2 model and the retrieval algorithm.

  5. Ground level environmental protein concentrations in various ecuadorian environments: potential uses of aerosolized protein for ecological research

    Science.gov (United States)

    Staton, Sarah J.R.; Woodward, Andrea; Castillo, Josemar A.; Swing, Kelly; Hayes, Mark A.

    2014-01-01

    Large quantities of free protein in the environment and other bioaerosols are ubiquitous throughout terrestrial ground level environments and may be integrative indicators of ecosystem status. Samples of ground level bioaerosols were collected from various ecosystems throughout Ecuador, including pristine humid tropical forest (pristine), highly altered secondary humid tropical forest (highly altered), secondary transitional very humid forest (regrowth transitional), and suburban dry montane deforested (suburban deforested). The results explored the sensitivity of localized aerosol protein concentrations to spatial and temporal variations within ecosystems, and their value for assessing environmental change. Ecosystem specific variations in environmental protein concentrations were observed: pristine 0.32 ± 0.09 μg/m3, highly altered 0.07 ± 0.05 μg/m3, regrowth transitional 0.17 ± 0.06 μg/m3, and suburban deforested 0.09 ± 0.04 μg/m3. Additionally, comparisons of intra-environmental differences in seasonal/daily weather (dry season 0.08 ± 0.03 μg/m3 and wet season 0.10 ± 0.04 μg/m3), environmental fragmentation (buffered 0.19 ± 0.06 μg/m3 and edge 0.15 ± 0.06 μg/m3), and sampling height (ground level 0.32 ± 0.09 μg/m3 and 10 m 0.24 ± 0.04 μg/m3) demonstrated the sensitivity of protein concentrations to environmental conditions. Local protein concentrations in altered environments correlated well with satellite-based spectral indices describing vegetation productivity: normalized difference vegetation index (NDVI) (r2 = 0.801), net primary production (NPP) (r2 = 0.827), leaf area index (LAI) (r2 = 0.410). Moreover, protein concentrations distinguished the pristine site, which was not differentiated in spectral indices, potentially due to spectral saturation typical of highly vegetated environments. Bioaerosol concentrations represent an inexpensive method to increase understanding of environmental changes, especially in densely vegetated

  6. Observations of the aerosol particle number concentration in the marine boundary layer over the south-eastern Baltic Sea

    Directory of Open Access Journals (Sweden)

    Dalia Jasinevičiene

    2013-08-01

    Full Text Available Continuous measurements of the aerosol particle number concentration (PNCin the size range from 4.5 nm to 2 µm were performed at the Preila marine background site during 2008–2009.The concentration maxima in summer was twice the average (2650±50 cm-3. A trajectory-based approach was applied for source identification. Potential Source Contribution Function (PSCFanalysis was performed to estimate the possible contribution of long-range andlocal PNC transport to PNC concentrations recorded at the marine backgroundsite. The PSCF results showed that the marine boundary layer was not seriouslyaffected by long-range transport, but that local transport of air pollutionwas recognized as an important factor. North Atlantic and Sea-Marine typeclusters respectively represented 32.1% and 17.9% of the total PNC spectraand were characterized by the lowest PNCs (1080±1340 and 1210±1040 cm-3 respectively among all clusters.   Wavelet transformation analysis of 1-h aerosol PNC indicated that whilethe 16-h scale was a constant feature of aerosol PNC evolution in spring, the longer (∼60-h scalesappeared mainly over the whole year (except June. Principal componentanalysis (PCA revealed a strong correlation between PNC and NaCl,highlighting the influence of sea-salt aerosols. In addition, PCA also showedthat PNC depended on optical and meteorological parameters such as UVR andtemperature.

  7. Characterisation of Fluorescent Biological Aerosol Particles during South-West Monsoon from a High Altitude Site in South India

    Science.gov (United States)

    Valsan, A. E.; R, R.; V, B. C.; Huffman, J. A.; Poeschl, U.; Gunthe, S. S.

    2015-12-01

    Biological aerosols (Bioaerosols) constitute a wide range of dead and alive biological materials that are suspended in the atmosphere. Though ubiquitous in earth's atmosphere, bioaerosols are poorly characterized in terms of their atmospheric abundance, sources and physical properties. Here we discuss the number concentration and size distribution of coarse mode (>1µm) biological aerosols measured at a relatively clean high altitude continental site, Munnar (10.09 N, 77.06 E; 1605 m asl) located in the Western Ghats mountain ranges of Southern Tropical India. The fluorescent biological aerosol particles (FBAP) were continuously measured using Ultra Violet Aerodynamic Particle Sizer (UVAPS) from 01 June to 21 August 2014 (South-West Monsoon Period) which showed some interesting patterns. The mean number and mass concentration of coarse FBAP during the campaign was observed to be 1.7 x 10-2cm-3 and 0.24µg m-3 respectively, which corresponds to 2% and 9% of coarse total aerosol particles (TAP) number and mass concentration. FBAP concentration decreased significantly during periods of heavy and continuous rain with constant South-West winds. This may be due to the clean marine influx coming from the ocean and continuous washout. The Relative Humidity (RH) and temperature remained consistent during this period without any strong diurnal pattern. When the wind fluctuated in North-West directions, the FBAP concentration increased to even an order of magnitude higher than the periods of South-West winds which can be attributed to the transported bioaerosols from the nearby vegetated area. In spite of variability in the number concentrations, the size distribution of FBAP exhibited a prominent peak at ~3 μm throughout the campaign, which should be fungal spores. They also exhibited a strong diurnal pattern with high concentrations occuring during the night time which peaks in the early morning hours.Biological aerosols (Bioaerosols) constitute a wide range of dead and

  8. Design and development of a high-concentration photovoltaic concentrator

    Energy Technology Data Exchange (ETDEWEB)

    Hodge, R C

    1982-04-01

    The design and development of a high concentration photovoltaic concentrator module is discussed. The design concept described herein incorporates a curved groove domed Fresnel lens, a high concentration etched multiple vertical junction (EMVJ) solar cell and a passively cooled direct-bonded copper cell mount all packaged in a plastic module. Two seven inch diameter 1200x domed Fresnel lenses were fabricated using single point diamond turning technology. Testing at both GE and Sandia confirmed optical transmission efficiencies of over 83%. Samples of the latest available EMVJ cells were mounted and installed, with a domed Fresnel lens, into a prototype module. Subsequent testing demonstrated net lens-cell efficiencies of 10 to 13%. As a result of this program, salient conclusions have been formulated as to this technology.

  9. The study of the evolution of aerosol concentrations at altitudes of civil aviation

    Science.gov (United States)

    Mamontov, Alexey; Gurvich, Alexander

    2017-04-01

    Clear Air Turbulence refers to turbulences in air without cloud, usually located in high troposphere and low stratosphere. Those CAT are a serious issue for inflight plane security and are responsible for numerous injuries or even reported deaths every year. Planes crossing such CAT can be strongly vertically shaken and passengers with security belt unfastened can be seriously injured. There is nowadays no alert system able to detect CAT at typical flight height. Indeed, onboard weather radars are blind to clear air turbulence. Today, Clear Air Turbulences are a serious flight security problem because there exists no ground or onboard detection devices. Besides, the physical phenomenon is far from being clearly understood. The understanding of CAT phenomenon is poor because: 1) is difficult to measure the CAT atmospheric parameters in situ (relatively low occurrence) 2) the simulations are complex. Therefore, this original project intends to 1) obtain a complete measured data set by remote sensing from the ground 2) join two different know-how to address the theoretical simulation aspects of CAT. Archive for the research was obtained in the performance of the European research program DELICAT (Demonstration of LIDAR based Clear Air Turbulence detection), which was a fullfledged performer IAP RAS(Obukhov Institute of atmospheric physics of Russian Academy of Science. The task of the flight test project DELICAT was to demonstrate the effectiveness of the proposed methods of lidar detection of turbulence. Flight tests were conducted using aircraft lidar instrument on board aircraft research vessel Cessna Citation II. Flight tests have given not only the information necessary to take into account the properties of airborne noise, but also provided us with data on atmospheric aerosol along the flight path. Questions aerosol scattering and the resulting data in this direction have not been claimed by European participants DELICAT. In practice many hours continuous

  10. Long-term aerosol measurements in Gran Canaria, Canary Islands: Particle concentration, sources and elemental composition

    Science.gov (United States)

    Gelado-Caballero, MaríA. D.; López-GarcíA, Patricia; Prieto, Sandra; Patey, Matthew D.; Collado, Cayetano; HéRnáNdez-Brito, José J.

    2012-02-01

    There are very few sets of long-term measurements of aerosol concentrations over the North Atlantic Ocean, yet such data is invaluable in quantifying atmospheric dust inputs to this ocean region. We present an 8-year record of total suspended particles (TSP) collected at three stations on Gran Canaria Island, Spain (Taliarte at sea level, Tafira 269 m above sea level (a.s.l.) and Pico de la Gorra 1930 m a.s.l.). Using wet and dry deposition measurements, the mean dust flux was calculated at 42.3 mg m-2 d-1. Air mass back trajectories (HYSPLIT, NOAA) suggested that the Sahara desert is the major source of African dust (dominant during 32-50% of days), while the Sahel desert was the major source only 2-10% of the time (maximum in summer). Elemental composition ratios of African samples indicate that, despite the homogeneity of the dust in collected samples, some signatures of the bedrocks can still be detected. Differences were found for the Sahel, Central Sahara and North of Sahara regions in Ti/Al, Mg/Al and Ca/Al ratios, respectively. Elements often associated with pollution (Pb, Cd, Ni, Zn) appeared to share a common origin, while Cu may have a predominantly local source, as suggested by a decrease in the enrichment factor (EF) of Cu during dust events. The inter-annual variability of dust concentrations is investigated in this work. During winter, African dust concentration measurements at the Pico de la Gorra station were found to correlate with the North Atlantic Oscillation (NAO) index.

  11. Evaluation and modeling of the size fractionated aerosol particle number concentration measurements nearby a major road in Helsinki ─ Part II: Aerosol measurements within the SAPPHIRE project

    Directory of Open Access Journals (Sweden)

    A. Karppinen

    2007-08-01

    Full Text Available This study presents an evaluation and modeling exercise of the size fractionated aerosol particle number concentrations measured nearby a major road in Helsinki during 23 August–19 September 2003 and 14 January–11 February 2004. The available information also included electronic traffic counts, on-site meteorological measurements, and urban background particle number size distribution measurement. The ultrafine particle (UFP, diameter<100 nm number concentrations at the roadside site were approximately an order of magnitude higher than those at the urban background site during daytime and downwind conditions. Both the modal structure analysis of the particle number size distributions and the statistical correlation between the traffic density and the UFP number concentrations indicate that the UFP were evidently from traffic related emissions. The modeling exercise included the evolution of the particle number size distribution nearby the road during downwind conditions. The model simulation results revealed that the evaluation of the emission factors of aerosol particles might not be valid for the same site during different time.

  12. A high-resolution study of surfactant partitioning and kinetic limitations for two-component internally mixed aerosols

    Science.gov (United States)

    Suda, S. R.; Petters, M. D.

    2013-12-01

    Atmospheric aerosols serve as cloud condensation nuclei (CCN), altering cloud properties and ultimately affecting climate through their effect on the radiative balance. Aerosol CCN activity depends in part on aerosol composition and surfactant compounds are of particular interest because surfactants are enriched at the water/air interface, resulting in a radial concentration gradient within the aqueous droplet. Accurate treatment of the surfactant concentration gradient complicates the otherwise straightforward predictions of CCN activity for aerosols of known composition. To accurately evaluate predictions made by theory, laboratory studies investigating the relationship between critical supersaturation and dry diameter of particles that include surfactants require significant reduction in measurement uncertainty for both water-uptake and CCN measurements. Furthermore, uncertainties remain regarding kinetic limitations to surfactant partitioning that could result in deviation from predictions based on equilibrium thermodynamics. This study attempts to address some of these issues through high-resolution analysis of CCN activity of two-component mixed surfactant/non-surfactant aerosols at different internal mixing ratios performed with and without a water-uptake time delay to ascertain whether or not the observed effects are kinetically limited. We present new data for the aerosols consisting of 1) the ionic surfactant sodium dodecyl sulfate (SDS) with ammonium sulfate, 2) SDS with sodium chloride and 3) the strong non-ionic fluorosurfactant Zonyl with an organic proxy glucose. As a point of reference we also evaluated the mixture of ammonium sulfate with glucose. Aerosol activation diameters were determined using CCN analysis in conjunction with scanning mobility size classification and high sheath-to-aerosol flow ratios. This resulted in CCN-derived kappa values that could be determined within +/-5% relative error. To test whether dynamic surfactant partitioning

  13. DMS atmospheric concentrations and sulphate aerosol indirect radiative forcing: a sensitivity study to the DMS source representation and oxidation

    Directory of Open Access Journals (Sweden)

    O. Boucher

    2003-01-01

    Full Text Available The global sulphur cycle has been simulated using a general circulation model with a focus on the source and oxidation of atmospheric dimethylsulphide (DMS. The sensitivity of atmospheric DMS to the oceanic DMS climatology, the parameterisation of the sea-air transfer and to the oxidant fields have been studied. The importance of additional oxidation pathways (by O3 in the gas- and aqueous-phases and by BrO in the gas phase not incorporated in global models has also been evaluated. While three different climatologies of the oceanic DMS concentration produce rather similar global DMS fluxes to the atmosphere at 24-27 Tg S yr -1, there are large differences in the spatial and seasonal distribution. The relative contributions of OH and NO3 radicals to DMS oxidation depends critically on which oxidant fields are prescribed in the model. Oxidation by O3 appears to be significant at high latitudes in both hemispheres. Oxidation by BrO could be significant even for BrO concentrations at sub-pptv levels in the marine boundary layer. The impact of such refinements on the DMS chemistry onto the indirect radiative forcing by anthropogenic sulphate aerosols is also discussed.

  14. Long-term observations of tropospheric particle number size distributions and equivalent black carbon mass concentrations in the German Ultrafine Aerosol Network (GUAN

    Directory of Open Access Journals (Sweden)

    W. Birmili

    2015-11-01

    Full Text Available The German Ultrafine Aerosol Network (GUAN is a cooperative atmospheric observation network, which aims at improving the scientific understanding of aerosol-related effects in the troposphere. The network addresses research questions dedicated to both, climate and health related effects. GUAN's core activity has been the continuous collection of tropospheric particle number size distributions and black carbon mass concentrations at seventeen observation sites in Germany. These sites cover various environmental settings including urban traffic, urban background, rural background, and Alpine mountains. In association with partner projects, GUAN has implemented a high degree of harmonisation of instrumentation, operating procedures, and data evaluation procedures. The quality of the measurement data is assured by laboratory intercomparisons as well as on-site comparisons with reference instruments. This paper describes the measurement sites, instrumentation, quality assurance and data evaluation procedures in the network as well as the EBAS repository, where the data sets can be obtained (doi:10.5072/guan.

  15. Characterisation of high dose dry powder aerosols by cascade impaction and laser diffraction analysis

    NARCIS (Netherlands)

    Grasmeijer, F.; Hagedoorn, P.; Frijlink, H.W.; De Boer, A.H.

    2011-01-01

    Background: Developments in high dose dry powder inhalationcontinue to challenge the viability of pharmacopoeialmethods for drug aerosol characterisation. Especiallythe occurrence of bounce effects can cause the amount offines (<1 lm) to be highly overestimated in particle sizedistributions (PSDs) o

  16. Pilot Study of Inhaled Aerosols Targeted via Magnetic Alignment of High Aspect Ratio Particles in Rabbits

    Directory of Open Access Journals (Sweden)

    Gillian E. S. Redman

    2011-01-01

    Full Text Available Recently, inhaled pharmaceutical aerosols have seen increased investigation in the treatment of lung cancer, where the inability to deliver adequate therapeutic drug concentrations to tumour sites may be overcome with improved targeted delivery to the site of the tumour. In this study, the feasibility of magnetically targeted delivery of high aspect ratio particles loaded with iron oxide nanoparticles was studied in 19 New Zealand White rabbits. Half of the exposed rabbits had a magnetic field placed externally over their right lung. Iron sensitive magnetic resonance images of the lungs were acquired to determine the iron concentrations in the right and left lung of each animal. The right/left ratio increased in the middle and basal regions of the lung where, due to the morphology of the rabbit lung, this method of targeting is most effective. With further optimization, this technique could be an effective method for increasing the dose of drug delivered to a specific site within the lung.

  17. Worldwide impact of aerosol's time scale on the predicted long-term concentrating solar power potential

    National Research Council Canada - National Science Library

    Ruiz-Arias, Jose A; Gueymard, Christian A; Santos-Alamillos, Francisco J; Pozo-Vázquez, David

    2016-01-01

    ...% in some areas with high solar resource, which may result in detrimental consequences for the bankability of concentrating solar power projects. Recommendations for the use of either daily or monthly AOD data are provided on a geographical basis.

  18. High Resolution Aerosol Data from MODIS Satellite for Urban Air Quality Studies

    Science.gov (United States)

    Chudnovsky, A.; Lyapustin, A.; Wang, Y.; Tang, C.; Schwartz, J.; Koutrakis, P.

    2013-01-01

    The Moderate Resolution Imaging Spectroradiometer (MODIS) provides daily global coverage, but the 10 km resolution of its aerosol optical depth (AOD) product is not suitable for studying spatial variability of aerosols in urban areas. Recently, a new Multi-Angle Implementation of Atmospheric Correction (MAIAC) algorithm was developed for MODIS which provides AOD at 1 km resolution. Using MAIAC data, the relationship between MAIAC AOD and PM(sub 2.5) as measured by the 27 EPA ground monitoring stations was investigated. These results were also compared to conventional MODIS 10 km AOD retrievals (MOD04) for the same days and locations. The coefficients of determination for MOD04 and for MAIAC are R(exp 2) =0.45 and 0.50 respectively, suggested that AOD is a reasonably good proxy for PM(sub 2.5) ground concentrations. Finally, we studied the relationship between PM(sub 2.5) and AOD at the intra-urban scale (10 km) in Boston. The fine resolution results indicated spatial variability in particle concentration at a sub-10 kilometer scale. A local analysis for the Boston area showed that the AOD-PM(sub 2.5) relationship does not depend on relative humidity and air temperatures below approximately 7 C. The correlation improves for temperatures above 7 - 16 C. We found no dependence on the boundary layer height except when the former was in the range 250-500 m. Finally, we apply a mixed effects model approach to MAIAC aerosol optical depth (AOD) retrievals from MODIS to predict PM(sub 2.5) concentrations within the greater Boston area. With this approach we can control for the inherent day-to-day variability in the AOD-PM(sub 2.5) relationship, which depends on time-varying parameters such as particle optical properties, vertical and diurnal concentration profiles and ground surface reflectance. Our results show that the model-predicted PM(sub 2.5) mass concentrations are highly correlated with the actual observations (out-of-sample R(exp 2) of 0.86). Therefore, adjustment

  19. Tropospheric Vertical Profiles of Aerosol Optical, Microphysical and Concentration Properties in the Frame of the Hygra-CD Campaign (Athens, Greece 2014: A Case Study of Long-Range Transport of Mixed Aerosols

    Directory of Open Access Journals (Sweden)

    Papayannis Alexandros

    2016-01-01

    Full Text Available Combined multi-wavelength aerosol Raman lidar and sun photometry measurements were performed during the HYGRA-CD campaign over Athens, Greece during May-June 2014. The retrieved aerosol optical properties (3 aerosol backscatter at 355-532-1064 nm and 2 aerosol extinction profiles at 355-532 nm were used as input to an inversion code to retrieve the aerosol microphysical properties (effective radius reff and number concentration N using regularization techniques. Additionally, the volume concentration profile was derived for fine particles using the LIRIC code. In this paper we selected a complex case study of long-range transport of mixed aerosols (biomass burning particles mixed with dust arriving over Athens between 10-12 June 2014 in the 1.5-4 km height. Between 2-3 km height we measured mean lidar ratios (LR ranging from 45 to 58 sr (at 355 and 532 nm, while the Ångström exponent (AE aerosol extinction-related values (355nm/532nm ranged between 0.8-1.3. The retrieved values of reff and N ranged from 0.19±0.07 to 0.22±0.07 μm and 460±230 to 2200±2800 cm-3, respectively. The aerosol linear depolarization ratio (δ at 532 nm was lower than 5-7% (except for the Saharan dust cases, where δ~10-15%.

  20. A case study of the highly time-resolved evolution of aerosol chemical and optical properties in urban Shanghai, China

    Directory of Open Access Journals (Sweden)

    Y. Huang

    2013-04-01

    Full Text Available Characteristics of the chemical and optical properties of aerosols in urban Shanghai and their relationship were studied over a three-day period in October 2011. A suite of real-time instruments, including an Aerosol Time-Of-Flight Mass Spectrometer (ATOFMS, a Monitor for AeRosols and GAses (MARGA, a Cavity Ring Down Spectrometer (CRDS, a nephelometer and a Scanning Mobility Particle Sizer (SMPS, was employed to follow the quick changes of the aerosol properties within the 72 h sampling period. The origin of the air mass arriving in Shanghai during this period shifted from the East China Sea to the northwest area of China, offering a unique opportunity to observe the evolution of aerosols influenced by regional transport from the most polluted areas in China. According to the meteorological conditions and temporal characterizations of the chemical and optical properties, the sampling period was divided into three periods. During Period 1 (00:00–23:00 LT, 13 October, the aerosols in urban Shanghai were mainly fresh and the single scattering albedo varied negatively with the emission of elemental carbon, indicating that local sources dominated. Period 2 (23:00 LT on 13 October to 10:00 LT on 15 October was impacted by regionally transported pollutants and had the highest particulate matter (PM mass loading and the lowest particle acidity, characterized by large fractions of aged particles and high secondary ion (nitrate, sulfate and ammonium mass concentrations. Comparison between ATOFMS particle acidity and quantitative particle acidity by MARGA indicated the significance of semi-quantitative calculation in ATOFMS. Two sub-periods were identified in Period 2 based on the scattering efficiency of PM1 mass. Period 3 (from 10:00 LT on 15 October to 00:00 LT on 16 October had a low PM1/PM10 ratio and a new particle formation event. The comparison of these sub-periods highlights the influence of particle mixing state on aerosol optical properties

  1. Molecular composition of organic aerosols in central Amazonia: an ultra-high-resolution mass spectrometry study

    Science.gov (United States)

    Kourtchev, Ivan; Godoi, Ricardo H. M.; Connors, Sarah; Levine, James G.; Archibald, Alex T.; Godoi, Ana F. L.; Paralovo, Sarah L.; Barbosa, Cybelli G. G.; Souza, Rodrigo A. F.; Manzi, Antonio O.; Seco, Roger; Sjostedt, Steve; Park, Jeong-Hoo; Guenther, Alex; Kim, Saewung; Smith, James; Martin, Scot T.; Kalberer, Markus

    2016-09-01

    The Amazon Basin plays key role in atmospheric chemistry, biodiversity and climate change. In this study we applied nanoelectrospray (nanoESI) ultra-high-resolution mass spectrometry (UHRMS) for the analysis of the organic fraction of PM2.5 aerosol samples collected during dry and wet seasons at a site in central Amazonia receiving background air masses, biomass burning and urban pollution. Comprehensive mass spectral data evaluation methods (e.g. Kendrick mass defect, Van Krevelen diagrams, carbon oxidation state and aromaticity equivalent) were used to identify compound classes and mass distributions of the detected species. Nitrogen- and/or sulfur-containing organic species contributed up to 60 % of the total identified number of formulae. A large number of molecular formulae in organic aerosol (OA) were attributed to later-generation nitrogen- and sulfur-containing oxidation products, suggesting that OA composition is affected by biomass burning and other, potentially anthropogenic, sources. Isoprene-derived organosulfate (IEPOX-OS) was found to be the most dominant ion in most of the analysed samples and strongly followed the concentration trends of the gas-phase anthropogenic tracers confirming its mixed anthropogenic-biogenic origin. The presence of oxidised aromatic and nitro-aromatic compounds in the samples suggested a strong influence from biomass burning especially during the dry period. Aerosol samples from the dry period and under enhanced biomass burning conditions contained a large number of molecules with high carbon oxidation state and an increased number of aromatic compounds compared to that from the wet period. The results of this work demonstrate that the studied site is influenced not only by biogenic emissions from the forest but also by biomass burning and potentially other anthropogenic emissions from the neighbouring urban environments.

  2. Aerosol profile information from high resolution oxygen A-Band measurements from space

    Directory of Open Access Journals (Sweden)

    A. Geddes

    2014-06-01

    Full Text Available Aerosols are an important factor of the Earth climatic system and they play a key role for air quality and public health. Observations of the oxygen A-Band at 760 nm can provide information on the vertical distribution of aerosols from passive satellite sensors, that can be of great interest for operational monitoring applications with high coverage if the aerosol information is obtained with sufficient precision, accuracy and vertical resolution. To address this issue, retrieval simulations of the aerosol vertical profile retrieval from O2 A Band observations by GOSAT, the upcoming OCO-2 and Sentinel 5-P mission and the proposed CarbonSat mission have been carried out. Precise retrievals of AOD within the boundary layer were found to favour low resolution, high SNR instruments such as Sentinel-5 P, whereas higher resolution instruments such as OCO-2 showed greater performance at higher altitudes and in information content above the boundary layer. Accurate retrievals of the AOD in the 0–2 km range appears difficult from all studied instruments and the retrieval errors typically exceed a value of 0.05. Constraining the surface albedo is a promising and effective way of improving the retrieval of aerosol, but the required level of a priori knowledge is very high. Due to the limited information content of the aerosol profile retrieval, the use of a parameterised aerosol distribution has been assessed and we show that the AOD and height of an aerosol layer can be retrieved well if the aerosol layer is uplifted to the free troposphere but errors are often large for aerosol layers in the boundary layer. Additional errors will be introduced by incorrect assumptions on surface pressure and aerosol type which can both bias retrieved AOD and height by up to 40%. We conclude the aerosol profile retrievals from O2 A Band using existing or upcoming satellite sensors will only provide limited information on aerosols in the boundary layer but such

  3. Highly time-resolved chemical characterization of atmospheric submicron particles during 2008 Beijing Olympic Games using an Aerodyne High-Resolution Aerosol Mass Spectrometer

    Directory of Open Access Journals (Sweden)

    X.-F. Huang

    2010-05-01

    Full Text Available As part of Campaigns of Air Quality Research in Beijing and Surrounding Region–2008 (CAREBeijing-2008, an Aerodyne High-Resolution Time-of-Flight Aerosol Mass Spectrometer (HR-ToF-AMS was deployed in urban Beijing to characterize submicron aerosol particles during the time of 2008 Beijing Olympic Games and Paralytic Games (24 July to 20 September 2008. The campaign mean PM1 mass concentration was 63.1±39.8 μg m−3; the mean composition consisted of organics (37.9%, sulfate (26.7%, ammonium (15.9%, nitrate (15.8%, black carbon (3.1%, and chloride (0.87%. The average size distributions of the species (except BC were all dominated by an accumulation mode peaking at about 600 nm in vacuum aerodynamic diameter, and organics was characterized by an additional smaller mode extending below 100 nm. Positive Matrix Factorization (PMF analysis of the high resolution organic mass spectral dataset differentiated the organic aerosol into four components, i.e., hydrocarbon-like (HOA, cooking-related (COA, and two oxygenated organic aerosols (OOA-1 and OOA-2, which on average accounted for 18.1, 24.4, 33.7 and 23.7% of the total organic mass, respectively. The HOA was identified to be closely associated with primary combustion sources, while the COA mass spectrum showed high similarity to that measured from cooking aerosol emissions. The OOA components correspond to aged secondary organic aerosol. Although the two OOA components have similar elemental (O/C, H/C compositions, they display differences in mass spectra and time series which appear to correlate with the different source regions sampled during the campaign. Back trajectory clustering analysis indicated that the southerly air flows were associated with the highest PM1 pollution during the campaign. This result is similar to observations made in the summer of 2006, although the average PM1 concentration level for the southerly air flows is 31% lower than

  4. Vaporization front in the interaction of a high-energy laser with aerosols - A solitary wave

    Science.gov (United States)

    Lee, C. T.; Miller, T. G.

    1982-06-01

    If a high-energy laser beam were to propagate through highly absorbent aerosols, the aerosols might be subject to extinction by evaporation. This could occur, for instance, if a high-energy CO2 laser beam were to propagate through a medium containing a mist of water droplets. The incident energy would evaporate the droplets, thus increasing the transmission with time. In this paper, solitary waves are obtained as the asymptotic solution to the coupled nonlinear equations describing such an interaction.

  5. Daily spectral effects on concentrating PV solar cells as affected by realistic aerosol optical depth and other atmospheric conditions

    Science.gov (United States)

    Gueymard, Christian A.

    2009-08-01

    This contribution addresses the need for more information about the spectral effect affecting solar cells specifically designed for concentrating photovoltaic (CPV) applications. Spectral effects result from differences between the actual (dynamically variable) solar spectrum incident on a solar cell in the field and the standard (fixed) solar spectrum used for rating purposes. A methodology is proposed to quantify this spectral effect at any site where basic atmospheric information exists, and predict what semiconductor material(s) may benefit from operating under non-standard conditions. Using the same SMARTS radiative code as for the development of the improved reference spectrum for concentrating PV rating, an analysis of the spectral sensitivity of five specific PV technologies to varying atmospheric factors is presented, using simulated spectra at 5-nm resolution. (The alternative of using the average photon energy (APE) concept was also considered, but proved inappropriate in the present context.) The technologies investigated here include a 21.5%-efficient CIGS cell, a 22%-efficient crystalline silicon cell (both appropriate for low-concentration applications), as well as three high-performance multijunction cells, which are specifically designed for high-concentration applications. To the difference of most previous studies, the approach taken here considers realistic atmospheric conditions. The proposed Daily Spectral Enhancement Factor (DSEF) is obtained from a typical daily-average incident spectrum, which is purposefully weighted to minimize the incidence of large spectral effects at low sun. Calculations of DSEF are performed here at fifteen world sites from an atmospheric monitoring network. These sites have largely different latitudes and climates, and yet are all potentially interesting for CPV applications. Results are obtained for a typical clear day of January and July, and for each of the five PV technologies just mentioned. This analysis

  6. Development and testing of an aerosol-stratus cloud parameterization scheme for middle and high latitudes

    Energy Technology Data Exchange (ETDEWEB)

    Olsson, P.Q.; Meyers, M.P.; Kreidenweis, S.; Cotton, W.R. [Colorado State Univ., Fort Collins, CO (United States)

    1996-04-01

    The aim of this new project is to develop an aerosol/cloud microphysics parameterization of mixed-phase stratus and boundary layer clouds. Our approach is to create, test, and implement a bulk-microphysics/aerosol model using data from Atmospheric Radiation Measurement (ARM) Cloud and Radiation Testbed (CART) sites and large-eddy simulation (LES) explicit bin-resolving aerosol/microphysics models. The primary objectives of this work are twofold. First, we need the prediction of number concentrations of activated aerosol which are transferred to the droplet spectrum, so that the aerosol population directly affects the cloud formation and microphysics. Second, we plan to couple the aerosol model to the gas and aqueous-chemistry module that will drive the aerosol formation and growth. We begin by exploring the feasibility of performing cloud-resolving simulations of Arctic stratus clouds over the North Slope CART site. These simulations using Colorado State University`s regional atmospheric modeling system (RAMS) will be useful in designing the structure of the cloud-resolving model and in interpreting data acquired at the North Slope site.

  7. Using High-Resolution Airborne Remote Sensing to Study Aerosol Near Clouds

    Science.gov (United States)

    Levy, Robert; Munchak, Leigh; Mattoo, Shana; Marshak, Alexander; Wilcox, Eric; Gao, Lan; Yorks, John; Platnick, Steven

    2016-01-01

    The horizontal space in between clear and cloudy air is very complex. This so-called twilight zone includes activated aerosols that are not quite clouds, thin cloud fragments that are not easily observable, and dying clouds that have not quite disappeared. This is a huge challenge for satellite remote sensing, specifically for retrieval of aerosol properties. Identifying what is cloud versus what is not cloud is critically important for attributing radiative effects and forcings to aerosols. At the same time, the radiative interactions between clouds and the surrounding media (molecules, surface and aerosols themselves) will contaminate retrieval of aerosol properties, even in clear skies. Most studies on aerosol cloud interactions are relevant to moderate resolution imagery (e.g. 500 m) from sensors such as MODIS. Since standard aerosol retrieval algorithms tend to keep a distance (e.g. 1 km) from the nearest detected cloud, it is impossible to evaluate what happens closer to the cloud. During Studies of Emissions, Atmospheric Composition, Clouds and Climate Coupling by Regional Surveys (SEAC4RS), the NASA ER-2 flew with the enhanced MODIS Airborne Simulator (eMAS), providing MODIS-like spectral observations at high (50 m) spatial resolution. We have applied MODIS-like aerosol retrieval for the eMAS data, providing new detail to characterization of aerosol near clouds. Interpretation and evaluation of these eMAS aerosol retrievals is aided by independent MODIS-like cloud retrievals, as well as profiles from the co-flying Cloud Physics Lidar (CPL). Understanding aerosolcloud retrieval at high resolution will lead to better characterization and interpretation of long-term, global products from lower resolution (e.g.MODIS) satellite retrievals.

  8. Characterization of submicron aerosols during a serious pollution month in Beijing (2013 using an aerodyne high-resolution aerosol mass spectrometer

    Directory of Open Access Journals (Sweden)

    J. K. Zhang

    2013-07-01

    Full Text Available In January 2013, Beijing experienced several serious haze events. To achieve a better understanding of the characteristics, sources and processes of aerosols during this month, an Aerodyne High-Resolution Time-of-Flight Aerosol Mass Spectrometer (HR-ToF-AMS was deployed at an urban site between 1 January and 1 February 2013 to obtain the size-resolved chemical composition of non-refractory submicron particles (NR-PM1. During this period, the mean measured NR-PM1 mass concentration was 87.4 μg m-3 and was composed of organics (49.8%, sulfate (21.4%, nitrate (14.6%, ammonium (10.4%, and chloride (3.8%. Moreover, inorganic matter, such as sulfate and nitrate comprised an increasing fraction of the NR-PM1 load as NR-PM1 loading increased, denoting their key roles in particulate pollution during this month. The average size distributions of the species were all dominated by an accumulation mode peaking at approximately 600 nm in vacuum aerodynamic diameter and organics characterized by an additional smaller size (∼200 nm. Elemental analyses showed that the average O/C, H/C, and N/C (molar ratio of organic matter were 0.34, 1.44 and 0.015, respectively, corresponding to an OM/OC ratio (mass ratio of organic matter to organic carbon of 1.60. Positive matrix factorization (PMF analyses of the high-resolution organic mass spectral dataset differentiated the organic aerosol into four components, i.e., oxygenated organic aerosols (OOA, cooking-related (COA, nitrogen-containing (NOA and hydrocarbon-like (HOA, which on average accounted for 40.0, 23.4, 18.1 and 18.5% of the total organic mass, respectively. Back trajectory clustering analyses indicated that the WNW air masses were associated with the highest NR-PM1 pollution during the campaign. Aerosol particles in southern air masses were especially rich in inorganic and oxidized organic species, whereas northern air masses contained a large fraction of primary species.

  9. Producing a highly concentrated coal suspension

    Energy Technology Data Exchange (ETDEWEB)

    Mokudzu, K.; Atsudzima, T.; Kiyedzuka, Y.

    1983-06-03

    Coal from wet and dry grinding is loaded into a mixer with a mixer arm with the acquisition of a highly concentrated suspension. Foamers (for instance, alkylbenzolsulfonate) and foam stabilizers (for instance diethanolamide of lauric acid) are added in a ratio of 10 to (2 to 5). The high fluidity of the suspension is maintained by injecting air into the suspension and an 80 percent concentration of the suspension is achieved.

  10. Factor analysis of combined organic and inorganic aerosol mass spectra from high resolution aerosol mass spectrometer measurements

    Directory of Open Access Journals (Sweden)

    Y. L. Sun

    2012-05-01

    Full Text Available The high resolution mass spectra of organic and inorganic aerosols from aerosol mass spectrometer (AMS measurements were first combined into positive matrix factorization (PMF analysis to investigate the sources and evolution processes of atmospheric aerosols. The new approach is able to study the mixing of organic aerosols (OA and inorganic species, the acidity of OA factors, and the fragment ion patterns related to photochemical processing. In this study, PMF analysis of the unified AMS spectral matrices resolved 8 factors for the submicron aerosols measured at Queens College in New York City in summer 2009. The hydrocarbon-like OA (HOA and cooking OA (COA contain very minor inorganic species, indicating the different sources and mixing characteristics between primary OA and secondary species. The two factors that are primarily ammonium sulfate (SO4-OA and ammonium nitrate (NO3-OA, respectively, are overall neutralized, of which the OA in SO4-OA shows the highest oxidation state (O/C = 0.69 among OA factors. The semi-volatile oxygenated OA comprises two components, i.e., a less oxidized (LO-OOA and a more oxidized (MO-OOA. The MO-OOA represents a local photochemical product with the diurnal profile exhibiting a pronounced noon peak, consistent with those of formaldehyde (HCHO and Ox (= O3+NO2. The much higher NO+/NO2+ fragment ion ratio in MO-OOA than that from ammonium nitrate alone provides evidence for the formation of organic nitrates. The amine-related nitrogen-enriched OA (NOA contains ~25% of acidic inorganic salts, elucidating the formation of secondary OA from amines in acidic environments. The size distributions derived from 3-dimensional size-resolved mass spectra show distinct diurnal evolving behaviors for different OA factors, but overall a progressing evolution from smaller to larger particle mode as a function of oxidation states

  11. Effects of turbulence on warm clouds and precipitation with various aerosol concentrations

    Science.gov (United States)

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

    2015-02-01

    This study investigates the effects of turbulence-induced collision enhancement (TICE) on warm clouds and precipitation by changing the cloud condensation nuclei (CCN) number concentration using a two-dimensional dynamic model with bin microphysics. TICE is determined according to the Taylor microscale Reynolds number and the turbulent dissipation rate. The thermodynamic sounding used in this study is characterized by a warm and humid atmosphere with a capping inversion layer, which is suitable for simulating warm clouds. For all CCN concentrations, TICE slightly reduces the liquid water path during the early stage of cloud development and accelerates the onset of surface precipitation. However, changes in the rainwater path and in the amount of surface precipitation that are caused by TICE depend on the CCN concentrations. For high CCN concentrations, the mean cloud drop number concentration (CDNC) decreases and the mean effective radius increases due to TICE. These changes cause an increase in the amount of surface precipitation. However, for low CCN concentrations, changes in the mean CDNC and in the mean effective radius induced by TICE are small and the amount of surface precipitation decreases slightly due to TICE. A decrease in condensation due to the accelerated coalescence between droplets explains the surface precipitation decrease. In addition, an increase in the CCN concentration can lead to an increase in the amount of surface precipitation, and the relationship between the CCN concentration and the amount of surface precipitation is affected by TICE. It is shown that these results depend on the atmospheric relative humidity.

  12. Aerosol nucleation induced by a high energy particle beam

    DEFF Research Database (Denmark)

    Enghoff, Martin Andreas Bødker; Pedersen, Jens Olaf Pepke; Uggerhøj, Ulrik I.

    atmospheric conditions using a 580 MeV electron beam to ionize the volume of the reaction chamber. We find a clear and significant contribution from ion induced nucleation and consider this to be an unambiguous observation of the ion-effect on aerosol nucleation using a particle beam under conditions not far......The effect of ions in aerosol nucleation is a subject where much remains to be discovered. That ions can enhance nucleation has been shown by theory, observations, and experiments. However, the exact mechanism still remains to be determined. One question is if the nature of the ionization affects...... the nucleation. This is an essential question since many experiments have been performed using radioactive sources that ionize differently than the cosmic rays which are responsible for the majority of atmospheric ionization. Here we report on an experimental study of sulphuric acid aerosol nucleation under near...

  13. High-spectral-resolution radiometric measurements of aerosol extinction over an urban region in India

    Science.gov (United States)

    Devara, P. C. S.; Ramkumar, M.; Maheskumar, R. S.; Pandithurai, G.

    2001-06-01

    Concurrent observations of aerosol optical depth (AOD) were carried out using a high-spectral-resolution radiometer (HSRR) and solar radiometer (SR) at the Indian Institute of Tropical Meteorology (IITM), Pune, India, on all clear-sky days available during November 1995-February 1996. The HSRR observations were collected at 5 nm intervals throughout the 400-700 nm spectrum while the SR measurements were made at discrete wavelengths of 400, 600, 940, 1060 and 1630 nm. In order to study the effect of integrated spectral observations on the derived AODs as compared to such depths from a single spectrum, multi-spectral observations at 2 nm intervals were collected. The AODs and their wavelength dependence from the HSRR and SR are compared and fairly good agreement found. The HSRR derived AODs at 400 nm and 700 nm from the present data sets are compared with those obtained during the winters of 1993-94 and 1994-95. The results reveal greater AODs, indicating abundance of aerosol particle concentration, during 1995-96 as compared to 1993-94 and 1994-95.

  14. Automated high-volume aerosol sampling station for environmental radiation monitoring

    Energy Technology Data Exchange (ETDEWEB)

    Toivonen, H.; Honkamaa, T.; Ilander, T.; Leppaenen, A.; Nikkinen, M.; Poellaenen, R.; Ylaetalo, S

    1998-07-01

    An automated high-volume aerosol sampling station, known as CINDERELLA.STUK, for environmental radiation monitoring has been developed by the Radiation and Nuclear Safety Authority (STUK), Finland. The sample is collected on a glass fibre filter (attached into a cassette), the airflow through the filter is 800 m{sup 3}/h at maximum. During the sampling, the filter is continuously monitored with Na(I) scintillation detectors. After the sampling, the large filter is automatically cut into 15 pieces that form a small sample and after ageing, the pile of filter pieces is moved onto an HPGe detector. These actions are performed automatically by a robot. The system is operated at a duty cycle of 1 d sampling, 1 d decay and 1 d counting. Minimum detectable concentrations of radionuclides in air are typically 1Ae10 x 10{sup -6} Bq/m{sup 3}. The station is equipped with various sensors to reveal unauthorized admittance. These sensors can be monitored remotely in real time via Internet or telephone lines. The processes and operation of the station are monitored and partly controlled by computer. The present approach fulfils the requirements of CTBTO for aerosol monitoring. The concept suits well for nuclear material safeguards, too 10 refs.

  15. CCN concentrations and BC warming influenced by maritime ship emitted aerosol plumes over southern Bay of Bengal

    Science.gov (United States)

    Ramana, M. V.; Devi, Archana

    2016-08-01

    Significant quantities of carbon soot aerosols are emitted into pristine parts of the atmosphere by marine shipping. Soot impacts the radiative balance of the Earth-atmosphere system by absorbing solar-terrestrial radiation and modifies the microphysical properties of clouds. Here we examined the impact of black carbon (BC) on net warming during monsoon season over southern Bay-of-Bengal, using surface and satellite measurements of aerosol plumes from shipping. Shipping plumes had enhanced the BC concentrations by a factor of four around the shipping lane and exerted a strong positive influence on net warming. Compiling all the data, we show that BC atmospheric heating rates for relatively-clean and polluted-shipping corridor locations to be 0.06 and 0.16 K/day respectively within the surface layer. Emissions from maritime ships had directly heated the lower troposphere by two-and-half times and created a gradient of around 0.1 K/day on either side of the shipping corridor. Furthermore, we show that ship emitted aerosol plumes were responsible for increase in the concentration of cloud condensation nuclei (CCN) by an order of magnitude that of clean air. The effects seen here may have significant impact on the monsoonal activity over Bay-of-Bengal and implications for climate change mitigation strategies.

  16. An integrated approach using high time-resolved tools to study the origin of aerosols

    Energy Technology Data Exchange (ETDEWEB)

    Di Gilio, A. [Chemistry Department, University of Bari, via Orabona, 4, 70126 Bari (Italy); ARPA PUGLIA, Corso Trieste, 27, 70126 Bari (Italy); Gennaro, G. de, E-mail: gianluigi.degennaro@uniba.it [Chemistry Department, University of Bari, via Orabona, 4, 70126 Bari (Italy); ARPA PUGLIA, Corso Trieste, 27, 70126 Bari (Italy); Dambruoso, P. [Chemistry Department, University of Bari, via Orabona, 4, 70126 Bari (Italy); ARPA PUGLIA, Corso Trieste, 27, 70126 Bari (Italy); Ventrella, G. [Chemistry Department, University of Bari, via Orabona, 4, 70126 Bari (Italy)

    2015-10-15

    Long-range transport of natural and/or anthropogenic particles can contribute significantly to PM10 and PM2.5 concentrations and some European cities often fail to comply with PM daily limit values due to the additional impact of particles from remote sources. For this reason, reliable methodologies to identify long-range transport (LRT) events would be useful to better understand air pollution phenomena and support proper decision-making. This study explores the potential of an integrated and high time-resolved monitoring approach for the identification and characterization of local, regional and long-range transport events of high PM. In particular, the goal of this work was also the identification of time-limited event. For this purpose, a high time-resolved monitoring campaign was carried out at an urban background site in Bari (southern Italy) for about 20 days (1st–20th October 2011). The integration of collected data as the hourly measurements of inorganic ions in PM{sub 2.5} and their gas precursors and of the natural radioactivity, in addition to the analyses of aerosol maps and hourly back trajectories (BT), provided useful information for the identification and chemical characterization of local sources and trans-boundary intrusions. Non-sea salt (nss) sulfate levels were found to increase when air masses came from northeastern Europe and higher dispersive conditions of the atmosphere were detected. Instead, higher nitrate and lower nss-sulfate concentrations were registered in correspondence with air mass stagnation and attributed to local traffic source. In some cases, combinations of local and trans-boundary sources were observed. Finally, statistical investigations such as the principal component analysis (PCA) applied on hourly ion concentrations and the cluster analyses, the Potential Source Contribution Function (PSCF) and the Concentration Weighted Trajectory (CWT) models computed on hourly back-trajectories enabled to complete a cognitive

  17. Airborne high spectral resolution lidar observation of pollution aerosol during EUCAARI-LONGREX

    Directory of Open Access Journals (Sweden)

    S. Groß

    2012-10-01

    Full Text Available Airborne high spectral resolution lidar observations over Europe during the EUCAARI field experiment in May 2008 are analysed with respect to spatial distribution and optical properties of continental pollution aerosol. Continental aerosol is characterized by its depolarisation and lidar ratio. Mean values of 6%±1% for the particle linear depolarisation ratio, and 56 sr±6 sr for the lidar ratio were found for pollution aerosol. Both, lidar ratio and depolarisation ratio at 532 nm show virtually no variations for all analysed days during the measurement campaign.

  18. Characterization of submicron aerosols at a rural site in Pearl River Delta of China using an Aerodyne High-Resolution Aerosol Mass Spectrometer

    Directory of Open Access Journals (Sweden)

    X.-F. Huang

    2010-11-01

    Full Text Available The Pearl River Delta (PRD region in South China is one of the most economically developed regions in China, but it is also noted for its severe air pollution due to industrial/metropolitan emissions. In order to continuously improve the understanding and quantification of air pollution in this region, an intensive campaign was executed in PRD during October–November 2008. Here, we report and analyze Aerodyne High-Resolution Aerosol Mass Spectrometer measurements at Kaiping, a rural site downwind of the highly-polluted central PRD area, to characterize the general features of submicron particulate pollution in the regional air. The mean measured PM1 mass concentration was 33.1 ± 18.1 μg m−3 during the campaign and composed of organic matter (33.8%, sulfate (33.7%, ammonium (14.0%, nitrate (10.7%, black carbon (6.7%, and chloride (1.1%, which is characterized by high fractions of inorganic ions due to huge emissions of SO2 and NOx in PRD. The average size distributions of the species (except BC were all dominated by an accumulation mode peaking at ~450 nm in vacuum aerodynamic diameter. Calculations based on high-resolution organic mass spectra indicate that C, H, O, and N on average contributed 56.6, 7.0, 35.1, and 1.3% to the total organic mass, respectively, corresponding to an organic matter mass to organic carbon mass ratio (OM/OC of 1.77 ± 0.08. Based on the high-resolution organic mass spectral dataset observed, Positive Matrix Factorization (PMF analysis differentiated the organic aerosol into three components, i.e., biomass burning (BBOA and two oxygenated (LV-OOA and SV-OOA organic aerosols, which on average accounted for 24.5, 39.6 and 35.8% of the total organic mass, respectively. The BBOA showed strong features of biomass burning emissions and has been mainly attributed to field rice straw burning after harvest. The LV-OOA and SV-OOA were found to correspond to more aged (and thus

  19. Chemical composition, sources, and processes of urban aerosols during summertime in northwest China: insights from high-resolution aerosol mass spectrometry

    Science.gov (United States)

    Xu, J.; Zhang, Q.; Chen, M.; Ge, X.; Ren, J.; Qin, D.

    2014-12-01

    An Aerodyne high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS) was deployed along with a scanning mobility particle sizer (SMPS) and a multi-angle absorption photometer (MAAP) to measure the temporal variations of the mass loading, chemical composition, and size distribution of submicron particulate matter (PM1) in Lanzhou, northwest China, during 11 July-7 August 2012. The average (PM1 mass concentration including non-refractory (PM1 (NR-(PM1) measured by HR-ToF-AMS and black carbon (BC) measured by MAAP during this study was 24.5 μg m-3 (ranging from 0.86 to 105 μg m-3), with a mean composition consisting of 47% organics, 16% sulfate, 12% BC, 11% ammonium, 10% nitrate, and 4% chloride. Organic aerosol (OA) on average consisted of 70% carbon, 21% oxygen, 8% hydrogen, and 1% nitrogen, with the average oxygen-to-carbon ratio (O / C) of 0.33 and organic mass-to-carbon ratio (OM / OC) of 1.58. Positive matrix factorization (PMF) of the high-resolution organic mass spectra identified four distinct factors which represent, respectively, two primary OA (POA) emission sources (traffic and food cooking) and two secondary OA (SOA) types - a fresher, semi-volatile oxygenated OA (SV-OOA) and a more aged, low-volatility oxygenated OA (LV-OOA). Traffic-related hydrocarbon-like OA (HOA) and BC displayed distinct diurnal patterns, both with peak at ~ 07:00-11:00 (BJT: UTC +8), corresponding to the morning rush hours, while cooking-emission related OA (COA) peaked during three meal periods. The diurnal profiles of sulfate and LV-OOA displayed a broad peak between ~ 07:00 and 15:00, while those of nitrate, ammonium, and SV-OOA showed a narrower peak between ~ 08:00-13:00. The later morning and early afternoon maximum in the diurnal profiles of secondary aerosol species was likely caused by downward mixing of pollutants aloft, which were likely produced in the residual layer decoupled from the boundary layer during nighttime. The mass spectrum of SV-OOA was

  20. The Potential of The Synergy of Sunphotometer and Lidar Data to Validate Vertical Profiles of The Aerosol Mass Concentration Estimated by An Air Quality Model

    Directory of Open Access Journals (Sweden)

    Siomos N.

    2016-01-01

    Full Text Available Vertical profiles of the aerosol mass concentration derived by the Lidar/Radiometer Inversion Code (LIRIC, that uses combined sunphotometer and lidar data, were used in order to validate the aerosol mass concentration profiles estimated by the air quality model CAMx. Lidar and CIMEL measurements performed at the Laboratory of Atmospheric Physics of the Aristotle University of Thessaloniki, Greece (40.5N, 22.9E from the period 2013-2014 were used in this study.

  1. The Potential of The Synergy of Sunphotometer and Lidar Data to Validate Vertical Profiles of The Aerosol Mass Concentration Estimated by An Air Quality Model

    Science.gov (United States)

    Siomos, N.; Filioglou, M.; Poupkou, A.; Liora, N.; Dimopoulos, S.; Melas, D.; Chaikovsky, A.; Balis, D. S.

    2016-06-01

    Vertical profiles of the aerosol mass concentration derived by the Lidar/Radiometer Inversion Code (LIRIC), that uses combined sunphotometer and lidar data, were used in order to validate the aerosol mass concentration profiles estimated by the air quality model CAMx. Lidar and CIMEL measurements performed at the Laboratory of Atmospheric Physics of the Aristotle University of Thessaloniki, Greece (40.5N, 22.9E) from the period 2013-2014 were used in this study.

  2. Daily variation of organic aerosol concentration and composition in Seoul, Korea during KORUS pre-campaign

    Science.gov (United States)

    Shin, H. J.; Lee, J.; Choi, A. Y.; Park, S. M.; Park, J. S.; Song, I. H.; Hong, Y. D.

    2015-12-01

    Daily variation of Organic Aerosol (OA) as well as organic tracer compounds have been observed in aerosol samples collected during KORUS-AQ (Korea-US Air Quality Study) pre-campaign (From May 18 to June 12) in Seoul, Korea. NR-PM1 bounded OA was measured by HR-TOF-AMS (Aerodyne) and the temporal variation, composition of OA by family group characterization, and oxidation state of OA was studied. And to distinguish the source characteristics (such as HOA, COA, NOA, SV-OOA, LV-OOA, etc…) of the organic, AMS-PMF model will be used.For the observation of organic tracer compounds, solvent extractable fractions were analyzed by GC-MS. More than 80 organic compounds were detected in the aerosol samples and grouped by source characterized classes, including vehicular emission tracers, biomass burning tracers, coal emission tracers, secondary organic aerosol (SOA) tracers. The main objective of this study is evaluation of the validity of OA fractionation based on the AMS measurement. So, we will compare daily variation of OA composition measured by AMS with daily variation of organic tracer compounds. Further, we will specify source characteristics estimated using AMS-PMF model by comparing the results of source apportionment of OA using PMF of organic tracer compounds.

  3. Evaluation of applicability of high-resolution multiangle imaging photo-polarimetric observations for aerosol atmospheric correction

    Science.gov (United States)

    Kalashnikova, Olga; Garay, Michael; Xu, Feng; Diner, David; Seidel, Felix

    2016-07-01

    Multiangle spectro-polarimetric measurements have been advocated as an additional tool for better understanding and quantifying the aerosol properties needed for atmospheric correction for ocean color retrievals. The central concern of this work is the assessment of the effects of absorbing aerosol properties on remote sensing reflectance measurement uncertainty caused by neglecting UV-enhanced absorption of carbonaceous particles and by not accounting for dust nonsphericity. In addition, we evaluate the polarimetric sensitivity of absorbing aerosol properties in light of measurement uncertainties achievable for the next generation of multi-angle polarimetric imaging instruments, and demonstrate advantages and disadvantages of wavelength selection in the UV/VNIR range. In this work a vector Markov Chain radiative transfer code including bio-optical models was used to quantitatively evaluate in water leaving radiances between atmospheres containing realistic UV-enhanced and non-spherical aerosols and the SEADAS carbonaceous and dust-like aerosol models. The phase matrices for the spherical smoke particles were calculated using a standard Mie code, while those for non-spherical dust particles were calculated using the numerical approach developed for modeling dust for the AERONET network of ground-based sunphotometers. As a next step, we have developed a retrieval code that employs a coupled Markov Chain (MC) and adding/doubling radiative transfer method for joint retrieval of aerosol properties and water leaving radiance from Airborne Multiangle SpectroPolarimetric Imager-1 (AirMSPI-1) polarimetric observations. The AirMSPI-1 instrument has been flying aboard the NASA ER-2 high altitude aircraft since October 2010. AirMSPI typically acquires observations of a target area at 9 view angles between ±67° at 10 m resolution. AirMSPI spectral channels are centered at 355, 380, 445, 470, 555, 660, and 865 nm, with 470, 660, and 865 reporting linear polarization. We

  4. Artificial primary marine aerosol production: a laboratory study with varying water temperature, salinity and succinic acid concentration

    Directory of Open Access Journals (Sweden)

    J. Zábori

    2012-08-01

    Full Text Available Primary marine aerosols are an important component of the climate system, especially in the remote marine environment. With diminishing sea-ice cover, better understanding of the role of sea spray aerosol on climate in the polar regions is required. As for Arctic Ocean water, laboratory experiments with NaCl water confirm that a few degrees change in the water temperature (Tw gives a large change in the number of primary particles. Smaller particles with a dry diameter between 0.01 μm and 0.25 μm dominate the aerosol number density, but their relative dominance decreases with increasing water temperature from 0 °C where they represent 85–90% of the total aerosol number to 60–70% of the total aerosol number at 10 °C water temperature. This effect is most likely related to a change in physical properties and not to modification of sea water chemistry. A change of salinity between 15 g kg−1 and 35 g kg−1 showed no influence on the relative shape of a particle number size distribution, nor did a change in water temperature between 0 °C and 16 °C. An experiment where succinic acid was added to a NaCl water solution showed, that the number concentration of particles with Dp < 0.312 μm decreased by 43% when the succinic acid concentration in NaCl water at Tw = 0 °C was increased from 0 μmol l−1 to 2446 μmol l−1. Different organic constituents and perhaps inorganic substances resulted in a particle number shift towards larger particle sizes, when comparing a size distribution resulting from pure NaCl water to size distributions resulting from Arctic Ocean water and resulting from NaCl water with a succinic acid concentration of 2446 μmol l−1.

  5. Source bioaerosol concentration and rRNA gene-based identification of microorganisms aerosolized at a flood irrigation wastewater reuse site.

    Science.gov (United States)

    Paez-Rubio, Tania; Viau, Emily; Romero-Hernandez, Socorro; Peccia, Jordan

    2005-02-01

    Reuse of partially treated domestic wastewater for agricultural irrigation is a growing practice in arid regions throughout the world. A field sampling campaign to determine bioaerosol concentration, culturability, and identity at various wind speeds was conducted at a flooded wastewater irrigation site in Mexicali, Baja California, Mexico. Direct fluorescent microscopy measurements for total microorganisms, culture-based assays for heterotrophs and gram-negative enteric bacteria, and small-subunit rRNA gene-based cloning were used for microbial characterizations of aerosols and effluent wastewater samples. Bioaerosol results were divided into two wind speed regimens: (i) below 1.9 m/s, average speed 0.5 m/s, and (ii) above 1.9 m/s, average speed 4.5 m/s. Average air-borne concentration of total microorganisms, culturable heterotrophs, and gram-negative enteric bacteria were, respectively, 1.1, 4.2, and 6.2 orders of magnitude greater during the high-wind-speed regimen. Small-subunit rRNA gene clone libraries processed from samples from air and the irrigation effluent wastewater during a high-wind sampling event indicate that the majority of air clone sequences were more than 98% similar to clone sequences retrieved from the effluent wastewater sample. Overall results indicate that wind is a potential aerosolization mechanism of viable wastewater microorganisms at flood irrigation sites.

  6. Anthropogenic sources of aerosol particles in a football stadium: Real-time characterization of emissions from cigarette smoking, cooking, hand flares, and color smoke bombs by high-resolution aerosol mass spectrometry

    Science.gov (United States)

    Faber, Peter; Drewnick, Frank; Veres, Patrick R.; Williams, Jonathan; Borrmann, Stephan

    2013-10-01

    Aerosol particles from several anthropogenic sources associated with football stadia including cooking, cigarette smoking, burning of color smoke bombs and hand flares were analyzed by high-resolution aerosol mass spectrometry. The physical and chemical characteristics of these different aerosols, in particular the organic fraction, were explored in laboratory studies to obtain robust references. These data were compared with field campaign results from a Bundesliga (German football league) match in the Coface Arena (Mainz, Germany) on 20th April 2012. The field measurement revealed a strongly elevated mass concentration of organic aerosols (OA) compared to background levels showing a temporal structure clearly related to the match. PMF analysis established that during the football match event cigarette smoke was the predominant component of submicron organic aerosol (67% of total OA). Cooking emissions from food outlets within the stadium correlated well with the sales figures of the catering stations and were also found to be of relevance (24% of total OA) especially in the period before kickoff. Pyrotechnics were not observed during this football match and no signatures of these sources were found in the mass spectra from the stadium measurements. All species that were elevated during the football match returned to their initial background levels within one hour after the match had finished. This demonstrates a good ventilation capacity of the open-topped Coface Arena.

  7. Concentrations of mineral aerosol from desert to plains across the central Rocky Mountains, western United States

    Science.gov (United States)

    Reynolds, Richard L.; Munson, Seth M.; Fernandez, Daniel; Goldstein, Harland L.; Neff, Jason C.

    2016-12-01

    Mineral dusts can have profound effects on climate, clouds, ecosystem processes, and human health. Because regional dust emission and deposition in western North America are not well understood, measurements of total suspended particulate (TSP) from 2011 to 2013 were made along a 500-km transect of five remote sites in Utah and Colorado, USA. The TSP concentrations in μg m-3 adjusted to a 24-h period were relatively high at the two westernmost, dryland sites at Canyonlands National Park (mean = 135) and at Mesa Verde National Park (mean = 99), as well as at the easternmost site on the Great Plains (mean = 143). The TSP concentrations at the two intervening montane sites were less, with more loading on the western slope of the Rocky Mountains (Telluride, mean = 68) closest to the desert sites compared with the site on the eastern slope (Niwot Ridge, mean = 58). Dust concentrations were commonly highest during late winter-late spring, when Pacific frontal storms are the dominant causes of regional wind. Low concentrations (10), as revealed by relatively low average daily concentrations of fine (<5 μg m-3; PM2.5) and coarse (<10 μg m-3; PM2.5-10) fractions monitored at or near four sites. Standard air-quality measurements for PM2.5 and PM10 apparently do not capture the large majority of mineral-particulate pollution in the remote western interior U.S.

  8. Contributions of local sources, long-range and mountain wind transport for aerosols over an eastern Himalayan high-altitude station in India

    Science.gov (United States)

    Chatterjee, Abhijit; Sarkar, Chirantan; Singh, Ajay; Ghosh, Sanjay; Raha, Sibaji; Das, Sanat

    A long-term study (2010-2013) on aerosols mass concentrations (PM2.5), number concentrations of size segregated aerosols and mass concentration of total suspended black carbon aerosols has been made over Darjeeling (27.01 N, 88.15 E), a high altitude (2200 m asl) station at eastern Himalaya in India. Seasonal and diurnal variation of all types of aerosols, their chemical composition and source apportionment revealed that aerosols over this part of Himalaya are mainly of two types; locally generated and long-range transported aerosols. The diurnal variation of aerosols including black carbon showed distinct feature of up-slope mountain wind transport mainly during premonsoon (Mar-May) which brings aerosol particles from low land regions. This present study focuses on the estimation of the individual contributions from local emissions (LE), long-range transport (LRT) and mountain wind transport (MWT) towards the total aerosol loading over Darjeeling. Several strike events (called by local political party) were observed at Darjeeling over the entire period of study (2008-2013) when all the local activities (schools, colleges, offices, vehicular, industrial etc) were stopped fully. Most of the strike events occurred during premonsoon. We have observed three types of events during premonsoon over the entire study period; 1) strike events with the contribution of LRT+MWT with zero local emissions (LE=0), 2) normal days with the contribution of LE+LRT+MWT, 3) normal days with the contribution of LE+MWT with zero long-range contribution (LRT=0). On normal days, the diurnal variation of aerosols during premonsoon showed sharp morning and evening peaks associated to local anthropogenic activities with the effect of up-slope mountain wind during afternoon. During strike events, the morning and evening peaks were absent but a broad peak was observed during afternoon associated to up-slope mountain wind. The increase in aerosol concentrations during afternoon on strike days

  9. Ultraviolet Raman lidar for high-accuracy profiling of aerosol extinction coefficient

    Institute of Scientific and Technical Information of China (English)

    Fei Gao; Xiaoquan Song; Yufeng Wang; Yi Zhou; Dengxin Hua

    2009-01-01

    An ultraviolet (UV) Raman lidar system at 354.7 nm has been developed for accurately measuring the aerosol extinction profiles. A spectroscopic filter combining a high-spectral-resolution grating with two narrowband mirrors is used to separate the vibrational Raman scattering signal of N2 at a central wave-length of 386.7 nm and the elastic scattering signal at 354.7 nm. The aerosol extinction is derived from the Raman scattering of N2 and the elastic scattering by the use of Raman method and Klett method, respectively. The derived results of aerosol extinction are used to compare the difference of two retrieval methods, and the preliminary experiment shows that the Raman lidar system operated in analog detection mode has the capability of measuring aerosol profiles up to a height of 3 km with a laser energy of 250 mJ and an integration time of 8 min.

  10. Iodine isotopes (127I and 129I) in aerosols at high altitude Alp stations.

    Science.gov (United States)

    Jabbar, Tania; Steier, Peter; Wallner, Gabriele; Priller, Alfred; Kandler, Norbert; Kaiser, August

    2012-08-21

    Concentrations of gases and particulate matter have been proven to be affected by meteorological and geographical variables from urban locations to high mountain clean air sites. Following our previous research in Vienna, we summarize here new findings about concentration levels of iodine isotopes in aerosols collected at two Alpine meteorological stations, Sonnblick (Austria) and Zugspitze (Germany) during 2001. The present study mainly focuses on the effect of altitude on the anthropogenic concentration of (129)I and on the isotopic ratio (129)I/(127)I. Iodine was separated from matrix elements by using either an anion exchange method or solvent extraction, and was analyzed by ICP-MS and AMS. Over the altitude change from Vienna to Zugspitze and Sonnblick (202 m to 2962 m and 3106 m above sea level), stable iodine level decreased from an average of 0.94 ng m(-3) to 0.52 ng m(-3) and 0.62 ng m(-3), respectively. Similarly, (129)I concentrations at both Alpine stations were about 1 order of magnitude lower (10(4) atoms m(-3)) than values obtained for Vienna (10(5) atoms m(-3)) and reveal a strong vertical concentration gradient of (129)I. A high degree of variability is observed, which is due to wide variation in the origin of air masses. Furthermore, air trajectory analysis demonstrates the importance of large scale air transport mostly from southeast Europe for influencing Sonnblick whereas influence from northwest Europe is strong at Zugspitze. In contrast to (129)I, a higher concentration of (7)Be was found at higher altitude stations compared to Vienna which probably results from its production in the upper atmosphere.

  11. Size-resolved aerosol chemistry on Whistler Mountain, Canada with a High-Resolution Aerosol Mass Spectrometer during INTEX-B

    Directory of Open Access Journals (Sweden)

    Y. Sun

    2008-12-01

    Full Text Available An Aerodyne High Resolution Time-of-Flight Aerosol Mass Spectrometer (HR-ToF-AMS was deployed at the peak of Whistler Mountain (elevation 2182 m-MSL, British Columbia, from 19 April to 16 May 2006, as part of the Intercontinental Chemical Transport Experiment Phase B (INTEX-B campaign. The mass concentrations and size distributions of non-refractory submicron particle (NR-PM1 species (i.e., sulfate, nitrate, ammonium, chloride, and organics were measured in situ every 5 min. The HR-ToF-AMS results agreed well with collocated measurements. The average concentration of non-refractory submicron particulate matter (NR-PM1; 1.9 μg m−3 is similar to those observed at other remote, high elevation sites in North America. Episodes of enhanced aerosol loadings were observed, due to influences of regional and trans-Pacific transport of air pollution. Organics and sulfate were the dominant species, on average accounting for 55% and 30%, respectively, of the NR-PM1 mass. The average size distributions of sulfate and ammonium both showed a~large accumulation mode peaking around 500–600 nm in Dva while those of organic aerosol (OA and nitrate peaked at ~300 nm. The size differences suggest that sulfate and OA were mostly present in external mixtures from different source origins. We also quantitatively determined the elemental composition of OA using the high resolution mass spectra. Overall, OA at Whistler Peak was highly oxygenated, with an average organic-mass-to-organic-carbon ratio (OM/OC of 2.28±0.23 and an atomic ratio of oxygen-to-carbon (O/C of 0.83±0.17. The nominal formula for OA was C1H1.66N0.03O0.83 for the entire study. Two significant trans-Pacific dust events originated from Asia were observed at Whistler Peak during this study. While both events were characterized with significant enhancements of coarse mode particles and mineral

  12. Aerosol nucleation induced by a high energy particle beam

    DEFF Research Database (Denmark)

    Enghoff, Martin Andreas Bødker; Pedersen, Jens Olaf Pepke; Uggerhøj, Ulrik I.

    2011-01-01

    We have studied sulfuric acid aerosol nucleation in an atmospheric pressure reaction chamber using a 580 MeV electron beam to ionize the volume of the reaction chamber. We find a clear contribution from ion-induced nucleation and consider this to be the first unambiguous observation of the ion......-effect on aerosol nucleation using a particle beam under conditions that resemble the Earth's atmosphere. By comparison with ionization using a gamma source we further show that the nature of the ionizing particles is not important for the ion-induced component of the nucleation. This implies that inexpensive...... ionization sources - as opposed to expensive accelerator beams - can be used for investigations of ion-induced nucleation....

  13. Cellulase Inhibition by High Concentrations of Monosaccharides

    DEFF Research Database (Denmark)

    Hsieh, Chia-Wen; Cannella, David; Jørgensen, Henning

    2014-01-01

    that low free water availability contributes to cellulase inhibition. Of the hydrolytic enzymes involved, those acting on the cellulose substrate, that is, exo- and endoglucanases, were the most inhibited. The β -glucosidases were shown to be less sensitive to high monosaccharide concentrations except...

  14. Artificial primary marine aerosol production: a laboratory study with varying water temperature, salinity, and succinic acid concentration

    Directory of Open Access Journals (Sweden)

    J. Zábori

    2012-11-01

    Full Text Available Primary marine aerosols are an important component of the climate system, especially in the remote marine environment. With diminishing sea-ice cover, better understanding of the role of sea spray aerosol on climate in the polar regions is required. As for Arctic Ocean water, laboratory experiments with NaCl water confirm that a few degrees change in the water temperature (Tw gives a large change in the number of primary particles. Small particles with a dry diameter between 0.01 μm and 0.25 μm dominate the aerosol number density, but their relative dominance decreases with increasing water temperature from 0 °C where they represent 85–90% of the total aerosol number to 10 °C, where they represent 60–70% of the total aerosol number. This effect is most likely related to a change in physical properties and not to modification of sea water chemistry. A change of salinity between 15 g kg−1 and 35 g kg−1 did not influence the shape of a particle number size distribution. Although the magnitude of the size distribution for a water temperature change between 0 °C and 16 °C changed, the shape did not. An experiment where succinic acid was added to a NaCl water solution showed, that the number concentration of particles with 0.010 μm < Dp < 4.5 μm decreased on average by 10% when the succinic acid concentration in NaCl water at a water temperature of 0 °C was increased from 0 μmol L−1 to 94 μmol L−1. A shift to larger sizes in the particle number size distribution is observed from pure NaCl water to Arctic Ocean water. This is likely a consequence of organics and different inorganic salts present in Arctic Ocean water in addition to the NaCl.

  15. Temporal variability of mineral dust in southern Tunisia: analysis of 2 years of PM10 concentration, aerosol optical depth, and meteorology monitoring

    Science.gov (United States)

    Bouet, Christel; Taieb Labiadh, Mohamed; Bergametti, Gilles; Rajot, Jean Louis; Marticorena, Béatrice; Sekrafi, Saâd; Ltifi, Mohsen; Féron, Anaïs; des Tureaux, Thierry Henry

    2016-04-01

    The south of Tunisia is a region very prone to wind erosion. During the last decades, changes in soil management have led to an increase in wind erosion. In February 2013, a ground-based station dedicated to the monitoring of mineral dust (that can be seen in this region as a proxy of the erosion of soils by wind) was installed at the Institut des Régions Arides (IRA) of Médenine (Tunisia) to document the temporal variability of mineral dust concentrations. This station allows continuous measurements of surface PM10 concentration (TEOM™), aerosol optical depth (CIMEL sunphotometer), and total atmospheric deposition of insoluble dust (CARAGA automatic sampler). The simultaneous monitoring of meteorological parameters (wind speed and direction, relative humidity, air temperature, atmospheric pressure, and precipitations) allows to analyse the factors controlling the variations of mineral dust concentration from the sub-daily to the annual scale. The results from the two first years of measurements of PM10 concentration are presented and discussed. In average on year 2014, PM10 concentration is 56 μg m-3. However, mineral dust concentration highly varies throughout the year: very high PM10 concentrations (up to 1,000 μg m-3 in daily mean) are frequently observed during wintertime and springtime, hardly ever in summer. These episodes of high PM10 concentration (when daily average PM10 concentration is higher than 240 μg m-3) sometimes last several days. By combining local meteorological data, air-masses trajectories, sunphotometer measurements, and satellite imagery, the part of the high PM10concentration due to local emissions and those linked to an advection of dusty air masses by medium and long range transport from the Sahara desert is quantified.

  16. Size specific indoor aerosol deposition measurements and derived I/O concentrations ratios

    DEFF Research Database (Denmark)

    Fogh, C.L.; Byrne, M.A.; Roed, Jørn;

    1997-01-01

    The process of aerosol deposition on indoor surfaces has implications for human exposure to particulate contaminants of both indoor and outdoor origin. In the radiological context, current accident models assume a uniform Dose Reduction Factor (DRF) of 0.5 for indoor residence during the outdoor...... and dispersed in unfurnished and furnished rooms; the decay rate of the particles was then inferred from analysis of sequential air samples. Allowing for the differences in furnishing and level of occupancy between the tests, consistent aerosol deposition velocities were determined and, for furnished rooms...... with previous measurements of I/O ratios for fine and coarse particles. It was concluded that, for realistic dose estimates, a radioisotope-specific factor may be merited. (C) 1997 Elsevier Science Ltd....

  17. NASA LaRC airborne high spectral resolution lidar aerosol measurements during MILAGRO: observations and validation

    Directory of Open Access Journals (Sweden)

    L. I. Kleinman

    2009-07-01

    Full Text Available The NASA Langley Research Center (LaRC airborne High Spectral Resolution Lidar (HSRL measures vertical profiles of aerosol extinction, backscatter, and depolarization at both 532 nm and 1064 nm. In March of 2006 the HSRL participated in the Megacity Initiative: Local and Global Research Observations (MILAGRO campaign along with several other suites of instruments deployed on both aircraft and ground based platforms. This paper presents high spatial and vertical resolution HSRL measurements of aerosol extinction and optical depth from MILAGRO and comparisons of those measurements with similar measurements from other sensors and model predictions. HSRL measurements coincident with airborne in situ aerosol scattering and absorption measurements from two different instrument suites on the C-130 and G-1 aircraft, airborne aerosol optical depth (AOD and extinction measurements from an airborne tracking sunphotometer on the J-31 aircraft, and AOD from a network of ground based Aerosol Robotic Network (AERONET sun photometers are presented as a validation of the HSRL aerosol extinction and optical depth products. Regarding the extinction validation, we find bias differences between HSRL and these instruments to be less than 3% (0.01 km−1 at 532 nm, the wavelength at which the HSRL technique is employed. The rms differences at 532 nm were less than 50% (0.015 km−1. To our knowledge this is the most comprehensive validation of the HSRL measurement of aerosol extinction and optical depth to date. The observed bias differences in ambient aerosol extinction between HSRL and other measurements is within 15–20% at visible wavelengths, found by previous studies to be the differences observed with current state-of-the-art instrumentation (Schmid et al., 2006.

  18. NASA LaRC airborne high spectral resolution lidar aerosol measurements during MILAGRO: observations and validation

    Directory of Open Access Journals (Sweden)

    R. R. Rogers

    2009-04-01

    Full Text Available The NASA Langley Research Center (LaRC airborne High Spectral Resolution Lidar (HSRL measures vertical profiles of aerosol extinction, backscatter, and depolarization at both 532 nm and 1064 nm. In March of 2006 the HSRL participated in the Megacity Initiative: Local and Global Research Observations (MILAGRO campaign along with several other suites of instruments deployed on both aircraft and ground based platforms. This paper presents high spatial and vertical resolution HSRL measurements of aerosol extinction and optical depth from MILAGRO and comparisons of those measurements with similar measurements from other sensors and model predictions. HSRL measurements coincident with airborne in situ aerosol scattering and absorption measurements from two different instrument suites on the C-130 and G-1 aircraft, airborne aerosol optical depth (AOD and extinction measurements from an airborne tracking sunphotometer on the J-31 aircraft, and AOD from a network of ground based Aerosol Robotic Network (AERONET sun photometers are presented as a validation of the HSRL aerosol extinction and optical depth products. Regarding the extinction validation, we find bias differences between HSRL and these instruments to be less than 3% (0.01 km−1 at 532 nm, the wavelength at which the HSRL technique is employed. The rms differences at 532 nm were less than 50% (0.015 km−1. To our knowledge this is the most comprehensive validation of the HSRL measurement of aerosol extinction and optical depth to date. The observed bias differences in ambient aerosol extinction between HSRL and other measurements is within 15–20% at visible wavelengths, found by previous studies to be the differences observed with current state-of-the-art instrumentation (Schmid et al., 2006.

  19. Production Mechanisms, Number Concentration, Size Distribution. Chemical Composition, and Optical Properties of Sea Spray Aerosols

    Science.gov (United States)

    Meskhidze, Nicholas; Petters, Markus; Tsigaridis, Kostas; Bates. Tim; O'Dowd, Colin; Reid, Jeff; Lewis, Ernie R.; Gantt, Brett; Anguelova, Magdalena D.; Bhave, Prakash V.; hide

    2013-01-01

    Over forty scientists from six countries convened in Raleigh, NC on June 4-6 2012 to review the status and prospects of sea spray aerosol research. Participants were researchers from the oceanography and atmospheric science communities, including academia, private industry, and government agencies. The recommendations from the working groups are summarized in a science prioritization matrix that is meant to prioritize the research agenda and identify areas of investigation by the magnitude of their impact on proposed science questions. Str

  20. 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...

  1. High-dimensional entanglement concentration of twisted photon pairs High-dimensional entanglement concentration

    Science.gov (United States)

    Chen, L. X.; Wu, Q. P.

    2012-10-01

    Recently, Dada et al. reported on the experimental entanglement concentration and violation of generalized Bell inequalities with orbital angular momentum (OAM) [Nat. Phys. 7, 677 (2011)]. Here we demonstrate that the high-dimensional entanglement concentration can be performed in arbitrary OAM subspaces with selectivity. Instead of violating the generalized Bell inequalities, the working principle of present entanglement concentration is visualized by the biphoton OAM Klyshko picture, and its good performance is confirmed and quantified through the experimental Shannon dimensionalities after concentration.

  2. Relationship of ground-level aerosol concentration and atmospheric electric field at three observation sites in the Arctic, Antarctic and Europe

    Science.gov (United States)

    Kubicki, Marek; Odzimek, Anna; Neska, Mariusz

    2016-09-01

    Aerosol number concentrations in the particle size range from 10 nm to 1 μm and vertical electric field strength in the surface layer was measured between September 2012 and December 2013 at three observation sites: mid-latitude station Swider, Poland, and, for the first time, in Hornsund in the Arctic, Spitsbergen, and the Antarctic Arctowski station in the South Shetland Islands. The measurements of aerosol concentrations have been performed simultaneously with measurements of the electric field with the aim to assess the local effect of aerosol on the electric field Ez near the ground at the three stations which at present form a network of atmospheric electricity observatories. Measurements have been made regardless of weather conditions at Swider and Arctowski station and mostly on fair-weather days at Hornsund station. The monthly mean particle number concentrations varied between 580 and 2100 particles cm- 3 at Arctowski, between 90 and 1270 particles cm- 3 in Hornsund, and between 6700 and 14,000 particles cm- 3 in the middle latitude station Swider. Average diurnal variations of the ground-level electric field Ez and particle number concentrations in fair-weather conditions were independent of each other for Arctowski and Hornsund stations. At Swider station the diurnal variation is usually characterized by an increase of aerosol concentration in the evening which results in the increased electric field. The assumption of neglecting the influence of varying aerosol concentration on the variation of the electric field in the polar regions, often adopted in studies, is confirmed here by the observations at Arctowski and Hornsund. The results of aerosol observations are also compared with modelled aerosol concentrations for global atmospheric electric circuit models.

  3. High Resolution Modelling of Aerosols-Meteorology Interactions over Northern Europe and Arctic regions

    Science.gov (United States)

    Mahura, Alexander; Nuterman, Roman; Baklanov, Alexander

    2017-04-01

    Aerosols have influence on weather, air quality and climate. Multi-scale modelling, and especially long-range atmospheric transport, dispersion, and deposition of aerosols from remote sources is especially challenging in northern latitudes. It is due to complexity of meteorological, chemical and biological processes, their interactions and especially within and above the surface layer, linking to climate change, and influence on ecosystems. The online integrated meteorology-chemistry-aerosols model Enviro-HIRLAM (Environment - High Resolution Limited Area Model) was employed for evaluating spatio-temporal variability of atmospheric aerosols and their interactions and effects on meteorology with a focus on the Northern Europe and Arctic regions. The model setup covers domain having 510 x 568 grids of latitude vs. longitude, horizontal resolution of 0.15 deg, 40 vertical hybrid levels, time step of 360 sec, 6 h meteorological surface data assimilation. The model was run for January and July-August 2010 at DMI's CRAY-XC30 supercomputer. Emissions used are anthropogenic (ECLIPSE v5), shipping (combined AU_RCP and FMI), wildfires (IS4FIRES), and interactive sea salt, dust and DMS. The boundary conditions were obtained from ECMWF: for meteorology (from IFS at 0.15 and 0.25 deg. for summer and winter, respectively) and atmospheric composition (from MACC Reanalysis at 1.125 deg. resolution). The Enviro-HIRLAM model was employed in 4 modes: the reference run (e.g. without aerosols influence on meteorology) and 3 modified runs (direct aerosol effect (DAE), indirect aerosol effect (IDAE), and both effects DAE and IDAE included). The differences between the reference run and the runs with mentioned aerosol effects were estimated on a day-by-day, monthly and diurnal cycle bases over the domain, Arctic areas, European and Nordic countries. The results of statistical analyses are summarized and presented.

  4. Development and Applications of a New, High-Resolution, Operational MISR Aerosol Product

    Science.gov (United States)

    Garay, M. J.; Diner, D. J.; Kalashnikova, O.

    2014-12-01

    Since early 2000, the Multi-angle Imaging SpectroRadiometer (MISR) instrument on NASA's Terra satellite has been providing aerosol optical depth (AOD) and particle property retrievals at 17.6 km spatial resolution. Capitalizing on the capabilities provided by multi-angle viewing, the operational MISR algorithm performs well, with about 75% of MISR AOD retrievals falling within 0.05 or 20% × AOD of the paired validation data from the ground-based Aerosol Robotic Network (AERONET), and is able to distinguish aerosol particles by size and sphericity, over both land and water. These attributes enable a variety of applications, including aerosol transport model validation and global air quality assessment. Motivated by the adverse impacts of aerosols on human health at the local level, and taking advantage of computational speed advances that have occurred since the launch of Terra, we have implemented an operational MISR aerosol product with 4.4 km spatial resolution that maintains, and sometimes improves upon, the quality of the 17.6 km resolution product. We will describe the performance of this product relative to the heritage 17.6 km product, the global AERONET validation network, and high spatial density AERONET-DRAGON sites. Other changes that simplify product content, and make working with the data much easier for users, will also be discussed. Examples of how the new product demonstrates finer spatial variability of aerosol fields than previously retrieved, and ways this new dataset can be used for studies of local aerosol effects, will be shown.

  5. Submicron aerosol analysis and organic source apportionment in an urban atmosphere in Pearl River Delta of China using high-resolution aerosol mass spectrometry

    Science.gov (United States)

    He, Ling-Yan; Huang, Xiao-Feng; Xue, Lian; Hu, Min; Lin, Yun; Zheng, Jun; Zhang, Renyi; Zhang, Yuan-Hang

    2011-06-01

    The Pearl River Delta (PRD) region in South China is one of the most economically developed regions in China while also noted for its severe air pollution, especially in the urban environments. In order to understand in depth the aerosol chemistry and the emission sources in PRD, an Aerodyne high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS) was deployed at an urban site in the Hong Kong-Shenzhen metropolitan area between 25 October and 2 December 2009. Ten minute-resolved measurement data were analyzed, and an average mass concentration of 44.5 ± 34.0 μg m-3 was calculated for the entire campaign. On average, organic matter was the most abundant PM1 component accounting for 39.7% of the total mass, followed by sulfate (24.5%), black carbon (measured by aethalometer, 14.0%), ammonium (10.2%), nitrate (10.0%), and chloride (1.6%). Moreover, organic matter comprised an increasing fraction of the PM1 loading as the PM1 loading increased, denoting its key role in particulate pollution in this region. Calculations of organic elemental composition based on the high-resolution organic mass spectra obtained indicated that C, H, O, and N on average contributed 33.8%, 55.1%, 10.2%, and 0.9%, respectively, to the total atomic numbers of organic aerosol (OA), which corresponded to an OM/OC ratio (the ratio of organic matter mass/organic carbon mass) of 1.57 ± 0.08. Positive matrix factorization analysis was then conducted on the high-resolution organic mass spectral data set. Four OA components were identified, including a hydrocarbon-like (HOA), a biomass burning (BBOA), and two oxygenated (LV-OOA and SV-OOA) components, which on average accounted for 29.5%, 24.1%, 18.8%, and 27.6%, respectively, of the total organic mass. The HOA was found to have contributions from both fossil fuel combustion and cooking emissions, while the BBOA was well correlated with acetonitrile, a known biomass burning marker. The LV-OOA and SV-OOA corresponded to more aged and

  6. Highly time-resolved chemical characterization of atmospheric submicron particles during 2008 Beijing Olympic Games using an Aerodyne High-Resolution Aerosol Mass Spectrometer

    Directory of Open Access Journals (Sweden)

    X.-F. Huang

    2010-09-01

    Full Text Available As part of Campaigns of Air Quality Research in Beijing and Surrounding Region-2008 (CAREBeijing-2008, an Aerodyne High-Resolution Time-of-Flight Aerosol Mass Spectrometer (HR-ToF-AMS was deployed in urban Beijing to characterize submicron aerosol particles during the time of 2008 Beijing Olympic Games and Paralympic Games (24 July to 20 September 2008. The campaign mean PM1 mass concentration was 63.1 ± 39.8 μg m−3; the mean composition consisted of organics (37.9%, sulfate (26.7%, ammonium (15.9%, nitrate (15.8%, black carbon (3.1%, and chloride (0.87%. The average size distributions of the species (except BC were all dominated by an accumulation mode peaking at about 600 nm in vacuum aerodynamic diameter, and organics was characterized by an additional smaller mode extending below 100 nm. Positive Matrix Factorization (PMF analysis of the high resolution organic mass spectral dataset differentiated the organic aerosol into four components, i.e., hydrocarbon-like (HOA, cooking-related (COA, and two oxygenated organic aerosols (OOA-1 and OOA-2, which on average accounted for 18.1, 24.4, 33.7 and 23.7% of the total organic mass, respectively. The HOA was identified to be closely associated with primary combustion sources, while the COA mass spectrum and diurnal pattern showed similar characteristics to that measured for cooking emissions. The OOA components correspond to aged secondary organic aerosol. Although the two OOA components have similar elemental (O/C, H/C compositions, they display differences in mass spectra and time series which appear to correlate with the different source regions sampled during the campaign. Back trajectory clustering analysis indicated that the southerly air flows were associated with the highest PM1 pollution during the campaign. Aerosol particles in southern airmasses were especially rich in inorganic and oxidized organic species. Aerosol particles in northern airmasses

  7. Concentration, distribution and variation of polar organic aerosol tracers in Ya'an, a middle-sized city in western China

    Science.gov (United States)

    Li, Li; Dai, Dongjue; Deng, Shihuai; Feng, Jialiang; Zhao, Min; Wu, Jun; Liu, Lu; Yang, Xiaohui; Wu, Sishi; Qi, Hui; Yang, Gang; Zhang, Xiaohong; Wang, Yingjun; Zhang, Yanzong

    2013-02-01

    PM2.5 (particulate matter with an aerodynamic diameter fructose), sugar alcohols (arabitol, mannitol, erythritol, sorbitol and xylitol), anhydrosugars (levoglucosan, mannosan and galactosan) and malic acid were determined. The factors that could potentially affect the SOA tracer concentrations, i.e. trace gases (SO2, NOx, O3, NH3), aerosol acidity and meteorological parameters, were monitored. The results showed that the concentrations of total isoprene oxidation products were 72 and 82 ng/m3 at the two sampling locations, with 29 ± 18, 37 ± 9, 6 ± 2 ng/m3 at SAU and 57 ± 34, 33 ± 33, 4 ± 2 ng/m3 at BSSA for 2-methyltetrols, C5-alkene triols and 2-methylglyceric acid respectively. Compared with the concentrations of isoprene oxidation products, those of α-/β-pinene oxidation products and β-caryophyllinic acid were much lower, being 6 ± 33 and 0.5 ± 1.9 ng/m3 at SAU, and 9 ± 14 and 1.0 ± 1.2 ng/m3 at BSSA, respectively. The unique composition of isoprene oxidation products, particularly, the high concentrations of the C5-alkene triols and their relative abundances comparable to those of the 2-methyltetrols, are possibly due to the fact that they are formed through acid-catalyzed reactions of C5-epoxydiols on weak acidic aerosols. Moreover, sugars and sugar alcohols were measured in important fractions at the two study areas, with the median concentrations of 309.7 and 465.7 ng/m3 at SAU and BSSA, respectively. The high abundances of sugar and sugar alcohols in the study area are explained by the robust metabolism of microorganism in the fertile soil under the warm and moist climate as well as vigorous physiological activities of vegetations in the exuberant subtropical areas. The detected organic tracers accounted in total for 1.5-1.8% of organic carbon (OC) in the study atmosphere, and about 15-21% of the OC could in total be apportioned to biogenic aerosol sources and source processes.

  8. Development of unmanned aerial vehicle (UAV) based high altitude balloon (HAB) platform for active aerosol sampling

    Science.gov (United States)

    Lateran, S.; Sedan, M. F.; Harithuddin, A. S. M.; Azrad, S.

    2016-10-01

    The knowledge on the abundance and diversity of the minute particles or aerosols in the earth's stratosphere is still in its infancy as aerosol sampling at high-altitude still possess a lot of challenges. Thus far, high-altitude aerosol sampling has been conducted mostly using manned flights, which requires enormous financial and logistical resources. There had been researches for the utilisation of high altitude balloon (HAB) for active and passive aerosol samplings within the stratosphere. However, the gathered samples in the payload were either brought down by controlling the balloon air pressure or were just dropped with a parachute to slow the descend speed in order to reduce the impact upon landing. In most cases, the drop location of the sample are unfavorable such as in the middle of the sea, dense foliage, etc. Hence a system that can actively sample aerosols at high-altitude and improve the delivery method in terms of quality and reliability using unmanned aerial vehicle (UAV) is designed and tested in this study.

  9. Evaluation of bio-aerosols concentration in the different wards of three educational hospitals in Iran

    Directory of Open Access Journals (Sweden)

    Heshmatollah Nourmoradi

    2012-01-01

    Full Text Available Aims: The aim of this study was to evaluate the bioaerosols level in the various parts of three educational hospitals of Isfahan, Iran. Materials and Methods: The collection of bioaerosols (including bacterial and fungal microorganisms was carried out with one-stage Anderson sampler. The sampling was carried out at the height of 1.5 m from the floor of various hospitals wards (infectious, surgery, urology wards, and operating room. The volume of each sample was determined based on pre-tests carried and was about 50 L. After sampling, the samples were incubated and analyzed. The effect of various environmental conditions including humidity, temperature, and outdoor bioaerosol levels was also investigated. Results: The lowest numbers of fungal and bacterial concentration were obtained in operating rooms of the hospitals and the highest concentration was observed in infectious disease wards of hospital 1 and 2 and surgery ward of hospital 3. The bacterial concentration was observed to be higher in hospital wards than outdoor, except hospitals′ operating rooms. Conclusion: The findings showed that the bioaerosols level in the hospitals was relatively high. The higher levels of indoor bacteria than outdoor might be associated with the presence of patients, their activity, unsuitable ventilation, and disinfection. Therefore, environmental monitoring and control measures are required to improve hospital environmental quality especially in the wards with immune deficiency patients.

  10. Identification of columnar aerosol types under high aerosol optical depth conditions for a single AERONET site in Korea

    Science.gov (United States)

    Choi, Yongjoo; Ghim, Young Sung; Holben, B. N.

    2016-02-01

    Dominant aerosol types were classified using level 2 inversion products for the Anmyon Aerosol Robotic Network (AERONET) site in Korea for the period 1999-2007. The aerosol types were mineral dust (MD), MD mixed with carbon, and black carbon mixed coarse particles (BCCP) for coarse mode aerosols, black carbon (BC), organic carbon (OC), and secondary inorganic ions (SII) for fine mode aerosols, and mixed particles between. The classification was carried out using a clustering method based on parameters, including single scattering albedo (SSA), absorption Angstrom exponent (AAE), and fine mode volume fraction (FMVF). Among the seven aerosol types, MD was distinct, with the highest AAE and a very low FMVF and SII with the highest SSA and FMVF. BCCP was introduced to designate coarse particles mixed with BC, of which the AAE was lower than 1, despite a low FMVF. In addition to a large difference in AAE between BC and OC, the SSA of OC was larger than that of BC, indicating the effects of the white smoke produced from the smoldering phase of biomass burning. Monthly variations of the aerosol types were well interpreted by meteorology and emissions and coincided with those in the previous studies. Applying our results to well-characterized global AERONET sites, we confirmed that the aerosol types at Anmyon were valid at other sites. However, the results also showed that the mean properties for aerosol types were influenced by the specific aerosols prevalent at the study sites.

  11. High Resolution Mass Spectrometry of Seasonal Aerosol Samples From an Urban Location in the Italian Po Valley

    Science.gov (United States)

    Mahon, Brendan; Giorio, Chiara; Gallimore, Peter J.; Zielinski, Arthur T.; Tapparo, Andrea; Kalberer, Markus

    2016-04-01

    The Po Valley in Northern Italy represents one of the most polluted environments in Europe, with PM2.5 and ozone concentrations regularly exceeding 100μg/m3 and 50ppb respectively. Particularly during winter, prolonged inversion conditions together with biomass burning and anthropogenic emissions regularly lead to severe air pollution events. Over the course of several months in 2013-14, we carried out a sampling program at a city-centre site in Padova, Italy, collecting 24-hour high-volume aerosol filter samples, 18 in winter (mid December - mid March) and 20 in summer (late May - late July). Utilising high-resolution Orbitrap mass spectrometry techniques, we have characterised these sample sets to examine the long-term variation in aerosol composition over the sampling campaign and to determine the effect of anthropogenic gaseous pollutants such as NOx and SO2 on the composition of organic particle components. The results showed that between ca. 450-700 ions were measured in each sample in both the summer and winter sample sets, however the majority (90%) of ions in the winter samples were below 300m/z and below 380m/z in the summer samples. A much higher percentage of CHO-only ions were found in winter (ca. 27%) compared to the summer samples (ca. 6%), indicating a higher degree of photochemical reactions taking place involving pollutants such as NOx and SO2 in summer. Our results represent the first long term data set of high-resolution measurements of aerosol composition and demonstrate that this technique is an important tool in evaluating the composition of aerosol particles in complex polluted urban areas.

  12. Changes in ground-level PM mass concentration and column aerosol optical depth over East Asia during 2004-2014

    Science.gov (United States)

    Nam, J.; Kim, S. W.; Park, R.; Yoon, S. C.; Sugimoto, N.; Park, J. S.; Hong, J.

    2015-12-01

    Multi-year records of moderate resolution imaging spectroradiometer (MODIS), ground-level particulate matter (PM) mass concentration, cloud-aerosol lidar with orthogonal polarization (CALIOP), and ground-level lidar were analyzed to investigate seasonal and annual changes of aerosol optical depth (AOD) and PM mass concentration over East Asia. Least mean square fit method is applied to detect the trends and their magnitudes for each selected regions and stations. Eleven-year MODIS measurements show generally increasing trends in both AOD (1.18 % yr-1) and Ångström exponent (0.98 % yr-1), especially over the east coastal industrialized region in China. Monthly variation of AOD show maximum value at April-July, which were related to the progress of summer monsoon rain band and stationary continental air mass on the northeast of Asia. Increasing trends of AOD were found for eight cites in China (0.80 % yr-1) and Seoul site, Korea (0.40 % yr-1), whereas no significant change were shown in Gosan background site (0.04 % yr-1) and decreasing trend at five background sites in Japan (-0.42 % yr-1). Contrasting to AOD trend, all fifteen sites in China (-1.28 % yr-1), Korea (-2.77 % yr-1), and Japan (-2.03 % yr-1) showed decreasing trend of PM10 mass concentration. Also, PM2.5 mass concentration at Beijing, Seoul, Rishiri, and Oki show significant decreasing trend of -1.16 % yr-1. To further discuss the opposite trend of surface PM mass concentration and column AOD, we investigate vertical aerosol profile from lidar measurements. AOD estimated for planetary boundary layer (surface~1.5 km altitude; AODPBL) from CALIOP measurements over East China show decreasing trend of -1.71 % yr-1 over the period of 2007-2014, wherever AOD estimated for free troposphere (1.5 km~5 km altitude; AODFT) show increasing trend of 2.92 % yr-1. In addition, ground-level lidar measurements in Seoul show decreasing AODPBL trend of -2.57 % yr-1, whereas, AODFT show no significant change (-0.44 % yr

  13. In Situ Measurements of Aerosol Mass Concentration and Spectral Absorption at Three Location in and Around Mexico City

    Science.gov (United States)

    Chaudhry, Z.; Martins, V.; Li, Z.

    2006-12-01

    As a result of population growth and increasing industrialization, air pollution in heavily populated urban areas is one of the central environmental problems of the century. As a part of the MILAGRO (Megacity Initiative: Local and Global Research Observations) study, Nuclepore filters were collected in two size ranges (PM10 and PM2.5) at 12 hour intervals at three location in Mexico during March, 2006. Sampling stations were located at the Instituto Mexicano del Petroleo (T0), at the Rancho La Bisnago in the State of Hidalgo (T2) and along the Gulf Coast in Tampico (Tam). Each filter was analyzed for mass concentration, aerosol scattering and absorption efficiencies. Mass concentrations at T0 ranged from 47 to 179 μg/m3 for PM10 with an average concentration of 96 μg/m3, and from 20 to 93 μg/m3 for PM2.5 with an average concentration of 41 μg/m3. Mass concentrations at T2 ranged from 12 to 154 μg/m3 for PM10 with an average concentration of 51 μg/m3, and from 7 to 50 μg/m3 for PM2.5 with an average concentration of 25 μg/m3. Mass concentrations at Tam ranged from 34 to 80 μg/m3 for PM10 with an average concentration of 52 μg/m3, and from 8 to 23 μg/m3 for PM2.5 with an average concentration of 13 μg/m3. While some of the extreme values are likely linked to local emissions, regional air pollution episodes also played important roles. Each of the sampling stations experienced a unique atmospheric condition. The site at T0 was influenced by urban air pollution and dust storms, the site at T2 was significantly less affected by air pollution but more affected by regional dust storms and local dust devils while Tam was influenced by air pollution, dust storms and the natural marine environment. The spectral mass absorption efficiency was measured from 350 to 2500 nm and shows large differences between the absorption properties of soil dust, black carbon, and organic aerosols. The strong spectral differences observed can be related to differences in

  14. Tropospheric distribution of sulphate aerosols mass and number concentration during INDOEX-IFP and its transport over the Indian Ocean: a GCM study

    Science.gov (United States)

    Verma, S.; Boucher, O.; Shekar Reddy, M.; Upadhyaya, H. C.; Le Van, P.; Binkowski, F. S.; Sharma, O. P.

    2012-07-01

    The sulphate aerosols mass and number concentration during the Indian Ocean Experiment (INDOEX) Intensive Field Phase-1999 (INDOEX-IFP) has been simulated using an interactive chemistry GCM. The model considers an interactive scheme for feedback from chemistry to meteorology with internally resolving microphysical properties of aerosols. In particular, the interactive scheme has the ability to predict both particle mass and number concentration for the Aitken and accumulation modes as prognostic variables. On the basis of size distribution retrieved from the observations made along the cruise route during IFP-1999, the model successfully simulates the order of magnitude of aerosol number concentration. The results show the southward migration of minimum concentrations, which follows ITCZ (Inter Tropical Convergence Zone) migration. Sulphate surface concentration during INDOEX-IFP at Kaashidhoo (73.46° E, 4.96° N) gives an agreement within a factor of 2 to 3. The measured aerosol optical depth (AOD) from all aerosol species at KCO was 0.37 ± 0.11 while the model simulated sulphate AOD ranged from 0.05 to 0.11. As sulphate constitutes 29% of the observed AOD, the model predicted values of sulphate AOD are hence fairly close to the measured values. The model thus has capability to predict the vertically integrated column sulphate burden. Furthermore, the model results indicate that Indian contribution to the estimated sulphate burden over India is more than 60% with values upto 40% over the Arabian Sea.

  15. Organic functional groups in aerosol particles from burning and non-burning forest emissions at a high-elevation mountain site

    Directory of Open Access Journals (Sweden)

    S. Takahama

    2011-07-01

    Full Text Available Ambient particles collected on teflon filters at the Peak of Whistler Mountain, British Columbia (2182 m a.s.l. during spring and summer 2009 were measured by Fourier transform infrared (FTIR spectroscopy for organic functional groups (OFG. The project mean and standard deviation of organic aerosol mass concentrations (OM for all samples was 3.2±3.3 (μg m−3. Measurements of aerosol mass fragments, size, and number concentrations were used to separate fossil-fuel combustion and burning and non-burning forest sources of the measured organic aerosol. The OM was composed of the same anthropogenic and non-burning forest components observed at Whistler mid-valley in the spring of 2008; during the 2009 campaign, biomass burning aerosol was additionally observed from fire episodes occurring between June and September. On average, organic hydroxyl, alkane, carboxylic acid, ketone, and primary amine groups represented 31 %±11 %, 34 %±9 %, 23 %±6 %, 6 %±7 %, and 6 %±3 % of OM, respectively. Ketones in aerosols were associated with burning and non-burning forest origins, and represented up to 27 % of the OM. The organic aerosol fraction resided almost entirely in the submicron fraction without significant diurnal variations. OM/OC mass ratios ranged mostly between 2.0 and 2.2 and O/C atomic ratios between 0.57 and 0.76, indicating that the organic aerosol reaching the site was highly aged and possibly formed through secondary formation processes.

  16. Radiocarbon-insights into temporal variations in the sources and concentrations of carbonaceous aerosols in the Los Angeles and Salt Lake City Metropolitan Areas

    Science.gov (United States)

    Czimczik, Claudia; Mouteva, Gergana; Simon, Fahrni; Guaciara, Santos; James, Randerson

    2014-05-01

    Increased fossil fuel consumption and biomass burning are contributing to significantly larger emissions of black carbon (BC) aerosols to the atmosphere. Together with organic carbon (OC), BC is a major constituent of fine particulate matter in urban air, contributes to haze and has been linked to a broad array of adverse health effects. Black carbon's high light absorption capacity and role in key (in-)direct climate feedbacks also lead to a range of impacts in the Earth system (e.g. warming, accelerated snow melt, changes in cloud formation). Recent work suggests that regulating BC emissions can play an important role in improving regional air quality and reducing future climate warming. However, BC's atmospheric transport pathways, lifetime and magnitudes of emissions by sector and region, particularly emissions from large urban centers, remain poorly constrained by measurements. Contributions of fossil and modern sources to the carbonaceous aerosol pool (corresponding mainly to traffic/industrial and biomass-burning/biogenic sources, respectively) can be quantified unambiguously by measuring the aerosol radiocarbon (14C) content. However, accurate 14C-based source apportionment requires the physical isolation of BC and OC, and minimal sample contamination with extraneous carbon or from OC charring. Compound class-specific 14C analysis of BC remains challenging due to very small sample sizes (5-15 ug C). Therefore, most studies to date have only analyzed the 14C content of the total organic carbonaceous aerosol fraction. Here, we present time-series 14C data of BC and OC from the Los Angeles (LA) metropolitan area in California - one of two megacities in the United States - and from Salt Lake City (SLC), UT. In the LA area, we analyzed 48h-PM10 samples near the LA port throughout 2007 and 2008 (with the exception of summer). We also collected monthly-PM2.5 samples at the University of California - Irvine, with shorter sampling periods during regional wildfire

  17. Eddy covariance measurements with high-resolution time-of-flight aerosol mass spectrometry: a new approach to chemically-resolved aerosol fluxes

    Directory of Open Access Journals (Sweden)

    D. K. Farmer

    2010-12-01

    Full Text Available Although laboratory studies show that biogenic volatile organic compounds (VOCs yield substantial secondary organic aerosol (SOA, production of biogenic SOA as indicated by upward fluxes has not been conclusively observed over forests. Further, while aerosols are known to deposit to surfaces, few techniques exist to provide chemically-resolved particle deposition fluxes. To better constrain aerosol sources and sinks, we have developed a new technique to directly measure fluxes of chemically-resolved submicron aerosols using the high-resolution time-of-flight aerosol mass spectrometer (HR-AMS in a new, fast eddy covariance mode. This approach takes advantage of the instrument's ability to quantitatively identify both organic and inorganic components, including ammonium, sulphate and nitrate, at a temporal resolution of several Hz. The new approach has been successfully deployed over a temperate ponderosa pine plantation in California during the BEARPEX-2007 campaign, providing both total and chemically resolved non-refractory (NR PM1 fluxes. Average deposition velocity for total NR-PM1 aerosol at noon was 2.05 ± 0.04 mm/s. Using a high resolution measurement of the NH2+ and NH3+ fragments, we demonstrate the first eddy covariance flux measurements of particulate ammonium, which show a noon-time deposition velocity of 1.9 ± 0.7 mm/s and are dominated by deposition of ammonium sulphate.

  18. High-time resolved measurements of biogenic and anthropogenic secondary organic aerosol precursors and products in urban air

    Science.gov (United States)

    Flores, Rosa M.; Doskey, Paul V.

    2016-04-01

    Volatile organic compounds (VOCs), which are present in the atmosphere entirely in the gas phase are directly emitted by biogenic (~1089 Tg yr-1) and anthropogenic sources (~185 Tg yr-1). However, the sources and molecular speciation of intermediate VOCs (IVOCs), which are for the most part also present almost entirely in the gas phase, are not well characterized. The VOCs and IVOCs participate in reactions that form ozone and semivolatile OC (SVOC) that partition into the aerosol phase. Formation and evolution of secondary organic aerosol (SOA) are part of a complex dynamic process that depends on the molecular speciation and concentration of VOCs, IVOCs, primary organic aerosol (POA), and the level of oxidants (NO3, OH, O3). The current lack of understanding of OA properties and their impact on radiative forcing, ecosystems, and human health is partly due to limitations of models to predict SOA production on local, regional, and global scales. More accurate forecasting of SOA production requires high-temporal resolution measurement and molecular characterization of SOA precursors and products. For the subject study, the IVOCs and aerosol-phase organic matter were collected using the high-volume sampling technique and were analyzed by multidimensional gas chromatography with time-of-flight mass spectrometry (GCxGC-ToFMS). The IVOCs included terpenes, terpenoids, n-alkanes, branched alkanes, isoprenoids, alkylbenzenes, cycloalkylbenzenes, PAH, alkyl PAH, and an unresolved complex mixture (UCM). Diurnal variations of OA species containing multiple oxygenated functionalities and selected SOA tracers of isorprene, α-pinene, toluene, cyclohexene, and n-dodecane oxidation were also quantified. The data for SOA precursor and oxidation products presented here will be useful for evaluating the ability of molecular-specific SOA models to forecast SOA production in and downwind of urban areas.

  19. Absorbing aerosols at high relative humidity: linking hygroscopic growth to optical properties

    Directory of Open Access Journals (Sweden)

    J. Michel Flores

    2012-06-01

    Full Text Available One of the major uncertainties in the understanding of Earth's climate system is the interaction between solar radiation and aerosols in the atmosphere. Aerosols exposed to high humidity will change their chemical, physical, and optical properties due to their increased water content. To model hydrated aerosols, atmospheric chemistry and climate models often use the volume weighted mixing rule to predict the complex refractive index (RI of aerosols when they interact with high relative humidity, and, in general, assume homogeneous mixing. This study explores the validity of these assumptions. A humidified cavity ring down aerosol spectrometer (CRD-AS and a tandem hygroscopic DMA (differential mobility analyzer are used to measure the extinction coefficient and hygroscopic growth factors of humidified aerosols, respectively. The measurements are performed at 80% and 90%RH at wavelengths of 532 nm and 355 nm using size-selected aerosols with different degrees of absorption; from purely scattering to highly absorbing particles. The ratio of the humidified to the dry extinction coefficients (fRHext(%RH, Dry is measured and compared to theoretical calculations based on Mie theory. Using the measured hygroscopic growth factors and assuming homogeneous mixing, the expected RIs using the volume weighted mixing rule are compared to the RIs derived from the extinction measurements.

    We found a weak linear dependence or no dependence of fRH(%RH, Dry with size for hydrated absorbing aerosols in contrast to the non-monotonically decreasing behavior with size for purely scattering aerosols. No discernible difference could be made between the two wavelengths used. Less than 7% differences were found between the real parts of the complex refractive indices derived and those calculated using the volume weighted mixing rule, and the imaginary parts had up to a 20% difference. However, for substances with growth factor less than 1

  20. A new method to discriminate secondary organic aerosols from different sources using high-resolution aerosol mass spectra

    Science.gov (United States)

    Heringa, M. F.; Decarlo, P. F.; Chirico, R.; Tritscher, T.; Clairotte, M.; Mohr, C.; Crippa, M.; Slowik, J. G.; Pfaffenberger, L.; Dommen, J.; Weingartner, E.; Prévôt, A. S. H.; Baltensperger, U.

    2012-02-01

    Organic aerosol (OA) represents a significant and often major fraction of the non-refractory PM1 (particulate matter with an aerodynamic diameter da car and a two-stroke Euro 2 scooter were characterized with an Aerodyne high-resolution time-of-flight aerosol mass spectrometer (HR-TOF-AMS) and compared to SOA from α-pinene. The emissions were sampled from the chimney/tailpipe by a heated inlet system and filtered before injection into a smog chamber. The gas phase emissions were irradiated by xenon arc lamps to initiate photo-chemistry which led to nucleation and subsequent particle growth by SOA production. Duplicate experiments were performed for each SOA type, with the averaged organic mass spectra showing Pearson's r values >0.94 for the correlations between the four different SOA types after five hours of aging. High-resolution mass spectra (HR-MS) showed that the dominant peaks in the MS, m/z 43 and 44, are dominated by the oxygenated ions C2H3O+ and CO2+, respectively, similarly to the relatively fresh semi-volatile oxygenated OA (SV-OOA) observed in the ambient aerosol. The atomic O:C ratios were found to be in the range of 0.25-0.55 with no major increase during the first five hours of aging. On average, the diesel SOA showed the lowest O:C ratio followed by SOA from wood burning, α-pinene and the scooter emissions. Grouping the fragment ions revealed that the SOA source with the highest O:C ratio had the largest fraction of small ions. The HR data of the four sources could be clustered and separated using principal component analysis (PCA). The model showed a significant separation of the four SOA types and clustering of the duplicate experiments on the first two principal components (PCs), which explained 79% of the total variance. Projection of ambient SV-OOA spectra resolved by positive matrix factorization (PMF) showed that this approach could be useful to identify large contributions of the tested SOA sources to SV-OOA. The first results from this

  1. High-sensitivity microchip electrophoresis determination of inorganic anions and oxalate in atmospheric aerosols with adjustable selectivity and conductivity detection.

    Science.gov (United States)

    Noblitt, Scott D; Schwandner, Florian M; Hering, Susanne V; Collett, Jeffrey L; Henry, Charles S

    2009-02-27

    A sensitive and selective separation of common anionic constituents of atmospheric aerosols, sulfate, nitrate, chloride, and oxalate, is presented using microchip electrophoresis. The optimized separation is achieved in under 1 min and at low background electrolyte ionic strength (2.9 mM) by combining a metal-binding electrolyte anion (17 mM picolinic acid), a sulfate-binding electrolyte cation (19 mM HEPBS), a zwitterionic surfactant with affinity towards weakly solvated anions (19 mM N-tetradecyl,N,N-dimethyl-3-ammonio-1-propansulfonate), and operation in counter-electroosmotic flow (EOF) mode. The separation is performed at pH 4.7, permitting pH manipulation of oxalate's mobility. The majority of low-concentration organic acids are not observed at these conditions, allowing for rapid subsequent injections without the presence of interfering peaks. Because the mobilities of sulfate, nitrate, and oxalate are independently controlled, other minor constituents of aerosols can be analyzed, including nitrite, fluoride, and formate if desired using similar separation conditions. Contact conductivity detection is utilized, and the limit of detection for oxalate (S/N=3) is 180 nM without stacking. Sensitivity can be increased with field-amplified sample stacking by injecting from dilute electrolyte with a detection limit of 19 nM achieved. The high-sensitivity, counter-EOF operation, and short analysis time make this separation well-suited to continuous online monitoring of aerosol composition.

  2. Vertical variability of aerosol single-scattering albedo and equivalent black carbon concentration based on in-situ and remote sensing techniques during the iAREA campaigns in Ny-Ålesund

    Science.gov (United States)

    Markowicz, K. M.; Ritter, C.; Lisok, J.; Makuch, P.; Stachlewska, I. S.; Cappelletti, D.; Mazzola, M.; Chilinski, M. T.

    2017-09-01

    This work presents a methodology for obtaining vertical profiles of aerosol single scattering properties based on a combination of different measurement techniques. The presented data were obtained under the iAREA (Impact of absorbing aerosols on radiative forcing in the European Arctic) campaigns conducted in Ny-Ålesund (Spitsbergen) during the spring seasons of 2015-2017. The retrieval uses in-situ observations of black carbon concentration and absorption coefficient measured by a micro-aethalometer AE-51 mounted onboard a tethered balloon, as well as remote sensing data obtained from sun photometer and lidar measurements. From a combination of the balloon-borne in-situ and the lidar data, we derived profiles of single scattering albedo (SSA) as well as absorption, extinction, and aerosol number concentration. Results have been obtained in an altitude range from about 400 m up to 1600 m a.s.l. and for cases with increased aerosol load during the Arctic haze seasons of 2015 and 2016. The main results consist of the observation of increasing values of equivalent black carbon (EBC) and absorption coefficient with altitude, and the opposite trend for aerosol concentration for particles larger than 0.3 μm. SSA was retrieved with the use of lidar Raman and Klett algorithms for both 532 and 880 nm wavelengths. In most profiles, SSA shows relatively high temporal and altitude variability. Vertical variability of SSA computed from both methods is consistent; however, some discrepancy is related to Raman retrieval uncertainty and absorption coefficient estimation from AE-51. Typically, very low EBC concentration in Ny-Ålesund leads to large error in the absorbing coefficient. However, SSA uncertainty for both Raman and Klett algorithms seems to be reasonable, e.g. SSA of 0.98 and 0.95 relate to an error of ±0.01 and ± 0.025, respectively.

  3. Molecular composition and volatility of isoprene photochemical oxidation secondary organic aerosol under low and high NOx conditions

    Energy Technology Data Exchange (ETDEWEB)

    D' Ambro, Emma; Lee, Ben H.; Liu, Jiumeng; Shilling, John E.; Gaston, Cassandra J.; Lopez-Hilfiker, Felipe D.; Schobesberger, Siegfried; Zaveri, Rahul A.; Mohr, Claudia; Lutz, Anna; Zhang, Zhenfa; Gold, Avram; Surratt, Jason D.; Rivera-Rios, Jean; Keutsch, Frank N.; Thornton, Joel A.

    2017-01-04

    We present measurements of secondary organic aerosol (SOA) formation from isoprene photochemical oxidation formed in an environmental simulation chamber using dry neutral seed particles, thereby suppressing the role of acid catalyzed multiphase chemistry, at a variety of oxidant conditions. A high-resolution time-of-flight chemical ionization mass spectrometer (HRToF-CIMS) utilizing iodide-adduct ionization coupled to the Filter Inlet for Gases and AEROsols (FIGAERO) allowed for the simultaneous online sampling of the gas and particle composition. Under high HO2 and low NO conditions, highly oxygenated (O:C ≥ 1) C5 compounds were major components (~50%) of the SOA. The overall composition of the SOA evolved both as a function of time and as a function of input NO concentrations. As the level of input NO increased, organic nitrates increased in both the gas- and particle-phases, but the dominant non-nitrate particle-phase components monotonically decreased. We use comparisons of measured and predicted gas-particle partitioning of individual components to assess the validity of literature-based group-contribution methods for estimating saturation vapor concentrations. While there is evidence for equilibrium partitioning being achieved on the chamber residence time scale (5.2 hours) for some individual components, significant errors in group-contribution methods are revealed. In addition, >30% of the SOA mass, detected as low-molecular weight compounds, cannot be reconciled with equilibrium partitioning. These compounds desorb from the FIGAERO at unexpectedly high temperatures given their molecular composition, indicative of thermal decomposition of effectively lower volatility components, likely larger molecular weight oligomers. We use these insights from the laboratory and observations of the same SOA components made during the Southern Oxidant and Aerosol Study (SOAS) to assess the importance of isoprene photooxidation as a local SOA source.

  4. Toxicity of atmospheric aerosols on marine phytoplankton

    Science.gov (United States)

    Paytan, A.; Mackey, K.R.M.; Chen, Y.; Lima, I.D.; Doney, S.C.; Mahowald, N.; Labiosa, R.; Post, A.F.

    2009-01-01

    Atmospheric aerosol deposition is an important source of nutrients and trace metals to the open ocean that can enhance ocean productivity and carbon sequestration and thus influence atmospheric carbon dioxide concentrations and climate. Using aerosol samples from different back trajectories in incubation experiments with natural communities, we demonstrate that the response of phytoplankton growth to aerosol additions depends on specific components in aerosols and differs across phytoplankton species. Aerosol additions enhanced growth by releasing nitrogen and phosphorus, but not all aerosols stimulated growth. Toxic effects were observed with some aerosols, where the toxicity affected picoeukaryotes and Synechococcus but not Prochlorococcus.We suggest that the toxicity could be due to high copper concentrations in these aerosols and support this by laboratory copper toxicity tests preformed with Synechococcus cultures. However, it is possible that other elements present in the aerosols or unknown synergistic effects between these elements could have also contributed to the toxic effect. Anthropogenic emissions are increasing atmospheric copper deposition sharply, and based on coupled atmosphere-ocean calculations, we show that this deposition can potentially alter patterns of marine primary production and community structure in high aerosol, low chlorophyll areas, particularly in the Bay of Bengal and downwind of South and East Asia.

  5. Ion concentrations of PM10–2.5 and PM2.5 aerosols over the eastern Mediterranean region: seasonal variation and source identification

    Directory of Open Access Journals (Sweden)

    N. A. Saliba

    2005-12-01

    Full Text Available The annual averages of particulate matters (PM10, PM10–2.5 (coarse and PM2.5 (fine in a densely populated area of Beirut were measured and found to be 84±27, 53±20 and 31±9 μg m−3, respectively. Ion Chromatography (IC analysis of the collected PM Teflon filters showed that NaCl, CaSO4 and Ca(NO32 were predominant in the coarse particles, while (NH42SO4 was the main salt in the fine particles. Using the non destructive Fourier Transform Infra Red-Attenuated Total Reflection (FTIR-ATR technique, CaCO3 was determined in the coarse filter. In addition, ATR measurements showed that inorganic salts present in the coarse particles are mostly water insoluble while salts found in fine particles are soluble. Concentrations of nitrates and calcium higher than the ones reported in neighboring Mediterranean countries were good indication of high traffic density and crustal dust abundance in Beirut, respectively. The study of the seasonal variation showed that long-range transport of SO2 from Eastern and Central Europe, sandy storms coming from Africa and marine aerosols are considered major sources of the determined inorganic ions. Considering the importance of the health and climate impacts of aerosols locally and regionally, this study constitutes a point of reference for eastern Mediterranean transport modeling studies and local regulatory and policy makers.

  6. Visibility-reducing organic aerosols in the vicinity of Grand Canyon National Park: Properties observed by high resolution gas chromatography

    OpenAIRE

    Mazurek, Monica A; Masonjones, Michael C.; Salmon, Lynn G.; Cass, Glen R.; Hallock, Kristen A.; Leach, Martin

    1997-01-01

    Fine particle and total airborne particle samples were collected during August 1989 within the Grand Canyon (Indian Gardens (IG)) and on its south rim (Hopi Point (HP)) to define summertime organic aerosol concentration and composition as a function of elevation at Grand Canyon National Park. Inorganic chemical constituents were analyzed also to help place the relative importance of organics in perspective. Fine particle organic aerosols were approximately equal in concentration to sulfate ae...

  7. Evidence for a High Proportion of Atmospheric Organic Aerosol from Isoprene

    Science.gov (United States)

    Robinson, Niall H.; Hamilton, Jacqueline F.; Langford, Ben; Oram, David E.; Barley, Mark H.; Jenkin, Michael E.; Rickard, Andrew R.; Coe, Hugh; McFiggans, Gordon

    2010-05-01

    The tropics emit a huge amount of volatile organic compounds (VOCs) into the Earth's atmosphere. The processes by which these gases are oxidised to form secondary organic aerosol (SOA) are currently not well understood or quantified. Intensive field measurements were carried out as part of the Oxidant and Particle Photochemical Processes (OP3) and the Aerosol Coupling in the Earth System (ACES) projects around pristine rainforest in Malaysian Borneo. This is the first campaign of its type in a South East Asian rainforest. We present detailed organic aerosol composition measurements made using an Aerodyne High Resolution Time of Flight Aerosol Mass Spectrometer (HR-ToF-AMS) at Bukit Atur, a Global Atmosphere Watch site located in the Danum Valley Conservation Area. This is a state-of-the-art field deployable instrument that can provide real time composition, mass loading and aerodynamic particle sizing information. In addition, the mass spectral resolution is sufficient to perform an analysis of the elemental composition of the organic species present. Off line analysis of filter samples was performed using comprehensive two-dimensional gas chromatography coupled to time of flight mass spectrometry (GCxGC/ToFMS). This technique provides a more detailed chemical characterisation of the SOA, allowing direct links back to gas phase precursors. The ground site data are compared with Aerodyne Compact Time of Flight Aerosol Mass Spectrometer (C-ToF-AMS) measurements made on the UK Facility for Airborne Atmospheric Measurements (FAAM) BAe-146 research aircraft. Airborne measurements were made above pristine rainforest surrounding the Danum Valley site, as well as nearby oil palm agricultural sites and palm oil rendering plants. Proton Transfer Reaction Mass Spectrometry (PTRMS) measurements of VOCs were made at the ground site and from the FAAM aircraft. Novel organic aerosol was measured by both AMSs, and identified as being isoprenoid in origin by GCxGC/ToFMS analysis

  8. Characterizing Aerosol Distributions and Optical Properties Using the NASA Langley High Spectral Resolution Lidar

    Energy Technology Data Exchange (ETDEWEB)

    Hostetler, Chris; Ferrare, Richard

    2013-02-14

    The objective of this project was to provide vertically and horizontally resolved data on aerosol optical properties to assess and ultimately improve how models represent these aerosol properties and their impacts on atmospheric radiation. The approach was to deploy the NASA Langley Airborne High Spectral Resolution Lidar (HSRL) and other synergistic remote sensors on DOE Atmospheric Science Research (ASR) sponsored airborne field campaigns and synergistic field campaigns sponsored by other agencies to remotely measure aerosol backscattering, extinction, and optical thickness profiles. Synergistic sensors included a nadir-viewing digital camera for context imagery, and, later in the project, the NASA Goddard Institute for Space Studies (GISS) Research Scanning Polarimeter (RSP). The information from the remote sensing instruments was used to map the horizontal and vertical distribution of aerosol properties and type. The retrieved lidar parameters include profiles of aerosol extinction, backscatter, depolarization, and optical depth. Products produced in subsequent analyses included aerosol mixed layer height, aerosol type, and the partition of aerosol optical depth by type. The lidar products provided vertical context for in situ and remote sensing measurements from other airborne and ground-based platforms employed in the field campaigns and was used to assess the predictions of transport models. Also, the measurements provide a data base for future evaluation of techniques to combine active (lidar) and passive (polarimeter) measurements in advanced retrieval schemes to remotely characterize aerosol microphysical properties. The project was initiated as a 3-year project starting 1 January 2005. It was later awarded continuation funding for another 3 years (i.e., through 31 December 2010) followed by a 1-year no-cost extension (through 31 December 2011). This project supported logistical and flight costs of the NASA sensors on a dedicated aircraft, the subsequent

  9. A new method to discriminate secondary organic aerosols from different sources using high-resolution aerosol mass spectra

    Directory of Open Access Journals (Sweden)

    M. F. Heringa

    2012-02-01

    Full Text Available Organic aerosol (OA represents a significant and often major fraction of the non-refractory PM1 (particulate matter with an aerodynamic diameter da < 1 μm mass. Secondary organic aerosol (SOA is an important contributor to the OA and can be formed from biogenic and anthropogenic precursors. Here we present results from the characterization of SOA produced from the emissions of three different anthropogenic sources. SOA from a log wood burner, a Euro 2 diesel car and a two-stroke Euro 2 scooter were characterized with an Aerodyne high-resolution time-of-flight aerosol mass spectrometer (HR-TOF-AMS and compared to SOA from α-pinene.

    The emissions were sampled from the chimney/tailpipe by a heated inlet system and filtered before injection into a smog chamber. The gas phase emissions were irradiated by xenon arc lamps to initiate photo-chemistry which led to nucleation and subsequent particle growth by SOA production.

    Duplicate experiments were performed for each SOA type, with the averaged organic mass spectra showing Pearson's r values >0.94 for the correlations between the four different SOA types after five hours of aging. High-resolution mass spectra (HR-MS showed that the dominant peaks in the MS, m/z 43 and 44, are dominated by the oxygenated ions C2H3O+ and CO2+, respectively, similarly to the relatively fresh semi-volatile oxygenated OA (SV-OOA observed in the ambient aerosol. The atomic O:C ratios were found to be in the range of 0.25–0.55 with no major increase during the first five hours of aging. On average, the diesel SOA showed the lowest O:C ratio followed by SOA from wood burning, α-pinene and the scooter emissions. Grouping the fragment ions revealed that the SOA source with the highest O:C ratio had the largest fraction of small ions.

    The HR data of the four sources could be clustered and separated using

  10. A new method to discriminate secondary organic aerosols from different sources using high-resolution aerosol mass spectra

    Directory of Open Access Journals (Sweden)

    M. F. Heringa

    2011-10-01

    Full Text Available Organic aerosol (OA represents a significant and often major fraction of the non-refractory PM1 (particulate matter with an aerodynamic diameter da < 1 μm mass. Secondary organic aerosol (SOA is an important contributor to the OA and can be formed from biogenic and anthropogenic precursors. Here we present results from the characterization of SOA produced from the emissions of three different anthropogenic sources. SOA from a log wood burner, a Euro 2 diesel car and a two-stroke Euro 2 scooter were characterized with an Aerodyne high-resolution time-of-flight aerosol mass spectrometer (HR-TOF-AMS and compared to SOA from α-pinene.

    The emissions were sampled from the chimney/tailpipe by a heated inlet system and filtered before injection into a smog chamber. The gas phase emissions were irradiated by xenon arc lamps to initiate photo-chemistry which led to nucleation and subsequent particle growth by SOA production.

    Duplicate experiments were performed for each SOA type, with the averaged organic mass spectra in the m/z range 12–250 showing Pearson's r values >0.94 for the correlations between the different SOA types after 5 h of aging. High-resolution mass spectra (HR-MS showed that the dominant peaks in the MS, m/z 43 and 44, are dominated by the oxygenated ions C2H3O+ and CO2+, respectively, similarly to the relatively fresh semi-volatile oxidized OA (SV-OOA observed in the ambient aerosol. The atomic O : C ratios were found to be in the range of 0.25–0.55 with no major increase during the first 5 h of aging. On average, the diesel SOA showed the lowest O : C ratio followed by SOA from wood burning, α-pinene and the scooter emissions. Grouping the fragment ions based on their carbon number revealed that the SOA source with the highest O : C ratio had the largest fraction of small ions. Fragment ions

  11. Fluorescent biological aerosol particle measurements at a tropical high-altitude site in southern India during the southwest monsoon season

    Science.gov (United States)

    Valsan, A. E.; Ravikrishna, R.; Biju, C. V.; Pöhlker, C.; Després, V. R.; Huffman, J. A.; Pöschl, U.; Gunthe, S. S.

    2016-08-01

    An ultraviolet aerodynamic particle sizer (UV-APS) was continuously operated for the first time during two seasons to sample the contrasting winds during monsoon and winter to characterize the properties of fluorescent biological aerosol particles (FBAPs), at a high-altitude site in India. Averaged over the entire monsoon campaign (1 June-21 August 2014), the arithmetic mean number and mass concentrations of coarse-mode (> 1 µm) FBAPs were 0.02 cm-3 and 0.24 µg m-3, respectively, which corresponded to ˜ 2 and 6 % of total aerosol loading, respectively. Average FBAP number size distribution exhibited a peak at ˜ 3 µm, which is attributed to the fungal spores, as supported by scanning electron microscope (SEM) images, and these results are consistent with previous studies made for FBAPs. During 11 weeks of measurements the variability of the total coarse-mode particle number (TAP) concentration was high compared to that observed in FBAP number concentrations. The TAP and FBAP number concentrations measured at this site were strongly dependent on changes in wind direction and rainfall. During periods of westerly/southwesterly winds with heavy persistent rainfall, the TAP and FBAP concentrations exhibited very low values (1.3 and 0.005 cm-3, respectively) with no significant diurnal variations, whereas during periods of northerly winds with scattered rainfall FBAPs exhibited relatively high concentration values (0.05 cm-3) with pronounced diurnal variations, which were strongly coupled with diurnal variations in meteorological parameters. The campaign-averaged FBAP number concentrations were shown to correlate with daily patterns of meteorological parameters and were positively correlated with relative humidity (RH; R2 = 0.58) and negatively with temperature (R2 = 0.60) and wind speed (R2 = 0.60). We did not observe any significant positive correlation with precipitation as reported by previous researchers from selected areas. These measurement results confirm the

  12. Diverse microbial species survive high ammonia concentrations

    Science.gov (United States)

    Kelly, Laura C.; Cockell, Charles S.; Summers, Stephen

    2012-04-01

    Planetary protection regulations are in place to control the contamination of planets and moons with terrestrial micro-organisms in order to avoid jeopardizing future scientific investigations relating to the search for life. One environmental chemical factor of relevance in extraterrestrial environments, specifically in the moons of the outer solar system, is ammonia (NH3). Ammonia is known to be highly toxic to micro-organisms and may disrupt proton motive force, interfere with cellular redox reactions or cause an increase of cell pH. To test the survival potential of terrestrial micro-organisms exposed to such cold, ammonia-rich environments, and to judge whether current planetary protection regulations are sufficient, soil samples were exposed to concentrations of NH3 from 5 to 35% (v/v) at -80°C and room temperature for periods up to 11 months. Following exposure to 35% NH3, diverse spore-forming taxa survived, including representatives of the Firmicutes (Bacillus, Sporosarcina, Viridibacillus, Paenibacillus, Staphylococcus and Brevibacillus) and Actinobacteria (Streptomyces). Non-spore forming organisms also survived, including Proteobacteria (Pseudomonas) and Actinobacteria (Arthrobacter) that are known to have environmentally resistant resting states. Clostridium spp. were isolated from the exposed soil under anaerobic culture. High NH3 was shown to cause a reduction in viability of spores over time, but spore morphology was not visibly altered. In addition to its implications for planetary protection, these data show that a large number of bacteria, potentially including spore-forming pathogens, but also environmentally resistant non-spore-formers, can survive high ammonia concentrations.

  13. Three years of aerosol mass, black carbon and particle number concentrations at Montsec (southern Pyrenees, 1570 m a.s.l.)

    Science.gov (United States)

    Ripoll, A.; Pey, J.; Minguillón, M. C.; Pérez, N.; Pandolfi, M.; Querol, X.; Alastuey, A.

    2014-04-01

    Time variation of mass particulate matter (PM1 and PM1&minus10), black carbon (BC) and number of particles (N3: number of particles with an aerodynamic diameter higher than 3 nm, and N10: higher than 10 nm) concentrations at the high-altitude site of Montsec (MSC) in the southern Pyrenees was interpreted for the period 2010-2012. At MSC, PM10 (12 μg m-3) and N7 (2140 # cm-3) three-year arithmetic average concentrations were higher than those measured at other high-altitude sites in central Europe during the same period (PM10: 3-9 μg m-3 and N: 634-2070 # cm-3). By contrast, BC concentrations at MSC (0.2 μg m-3) were equal to or even lower than those measured at these European sites (0.2-0.4 μg m-3). These differences were attributed to the higher relevance of Saharan dust transport and to the higher importance of the biogenic precursor emissions and new particle formation (NPF) processes, and to the lower influence of anthropogenic emissions at MSC. The different time variation of PM and BC concentrations compared with that of N suggests that these aerosol parameters were governed by diverse factors at MSC. Both PM and BC concentrations showed marked differences for different meteorological scenarios, with enhanced concentrations under North African air outbreaks (PM1&minus10: 13 μg m-3, PM1: 8 μg m-3 and BC: 0.3 μg m-3) and low concentrations when Atlantic advections occurred (PM1-10: 5 μg m-3, PM1: 4 μg m-3 and BC: 0.1 μg m-3). PM and BC concentrations increased in summer, with a secondary maximum in early spring, and were at their lowest in winter, due to the contrasting origin of the air masses in the warmer seasons (spring and summer) and in the colder seasons (autumn and winter). The maximum in the warmer seasons was attributed to long-range transport processes that mask the breezes and regional transport breaking the daily cycles of these pollutants. By contrast, PM and BC concentrations showed clear diurnal cycles, with maxima at midday in the

  14. Aerosol size distributions measured in urban, rural and high-alpine air with an electrical low pressure impactor (ELPI)

    Science.gov (United States)

    Held, A.; Zerrath, A.; McKeon, U.; Fehrenbach, T.; Niessner, R.; Plass-Dülmer, C.; Kaminski, U.; Berresheim, H.; Pöschl, U.

    An electrical low pressure impactor (ELPI) was used to study atmospheric aerosol particle number, surface, and mass concentrations and size distributions over a diameter range of 7 nm-10 μm at urban, rural and high-alpine locations along an alpine altitude transect across Southern Germany. The measurements were performed in the city of Munich and at the global atmosphere watch (GAW) stations Hohenpeißenberg and Zugspitze in the years 2001-2004. To minimize particle bounce effects and enable chemical analysis of the collected particles without disturbance by grease on the impaction substrates, the sample flow was conditioned to about 75% relative humidity. The performance of the ELPI instrument was evaluated by comparison with well-established aerosol measurement techniques including condensation particle counters, scanning and differential mobility particle sizers, filter sampling, and gravimetric determination of particulate mass. In general, particle number concentrations, size distributions, and PM2.5 concentrations determined with the ELPI were in good agreement with alternative techniques (rank correlation coefficients ρ = 0.70-0.95). The ELPI filter stage data for the particle diameter range of 7-30 nm, however, appeared to be strongly biased towards high values. Long-term measurements at the rural site (Hohenpeißenberg) revealed distinct seasonal patterns with the highest number concentrations in summer (median daily average: 3100 cm -3) and the highest mass concentrations in spring and fall (median daily average PM2.5 and PM10: 21-25 and 27-35 μg m -3, respectively). In spring and fall we also observed pronounced maxima of particle surface and mass concentration in the coarse mode (peak at ˜3 μm), which are most likely due to primary biological material. Relatively clean air (PM10 urban air from Munich (NE) clearly contributed to elevated particle mass loadings (PM10 > = 10 μg m -3).

  15. Comparison of high order algorithms in Aerosol and Aghora for compressible flows

    Directory of Open Access Journals (Sweden)

    Mbengoue D. A.

    2013-12-01

    Full Text Available This article summarizes the work done within the Colargol project during CEMRACS 2012. The aim of this project is to compare the implementations of high order finite element methods for compressible flows that have been developed at ONERA and at INRIA for about one year, within the Aghora and Aerosol libraries.

  16. Lab-scale development of a high temperature aerosol particle sampling probe system for field measurements in thermochemical conversion of biomass

    Energy Technology Data Exchange (ETDEWEB)

    Lindskog, M.; Malik, A.; Pagels, J.; Sanati, M. [Lund Univ., Lund (Sweden). Div. of Ergonomics and Aerosol Technology

    2010-07-01

    Thermochemical conversion of biomass requires both combustion in an oxygen rich environment and gasification in an oxygen deficient environment. Therefore, the mass concentration of fly ash from combustion processes is dominated by inorganic compounds, and the particulate matter obtained from gasification is dominated by carbonaceous compounds. The fine fly ash particles can initiate corrosion and fouling and also increases emissions of fine particulates to the atmosphere. This study involved the design of a laboratory scale setup consisting of a high temperature sampling probe and an aerosol generation system to study the formation of fine particle from biomass gasification processes. An aerosol model system using potassium chloride (KCl) as the ash compound and Di Octyl Sebacate oil (DOS) as the volatile organic part was used to test the high temperature sampling probe. Tests conducted at 200 degrees C showed good reproducibility of the aerosol generator. The tests also demonstrated suitable dilution ratios which enabled the denuder to absorb all of the gaseous organic compounds in the set up, thus enabling measurement of only the particle phase. Condensable organic concentrations of 1-68 mg/m{sup 3} were easily handled by the high temperature sampling probe system, indicating that the denuder worked well. Additional tests will be performed using an Aerosol Mass Spectrometer (AMST) to verify that the denuder can capture all of the gaseous organic compounds also when condensed onto agglomerated soot particles. 6 refs., 1 tab., 9 figs.

  17. Comparison of measurements of peroxyacyl nitrates and primary carbonaceous aerosol concentrations in Mexico City determined in 1997 and 2003

    Science.gov (United States)

    Marley, N. A.; Gaffney, J. S.; Ramos-Villegas, R.; Cárdenas González, B.

    2007-05-01

    The concentrations of peroxyacetyl nitrate (PAN) in ambient air can be a good indicator of air quality and the effectiveness of control strategies for reducing ozone levels in urban areas. As PAN is formed by the oxidation of reactive hydrocarbons in the presence of nitrogen dioxide (NO2), it is a direct measure of the peroxyacyl radical levels produced from reactive organic emissions in the urban air shed. Carbon soot, known as black carbon (BC) or elemental carbon (EC), is a primary atmospheric aerosol species and is a good indicator of the levels of combustion emissions, particularly from diesel engines, in major cities. Mexico City is the second largest megacity in the world and has long suffered from poor air quality. Reported here are atmospheric measurements of PAN and BC obtained in Mexico City during the Mexico Megacity 2003 field study. These results are compared with measurements obtained earlier during the Investigación sobre Materia Particulada y Deterioro Atmosférico - Aerosol and Visibility Research (IMADA-AVER) campaign in 1997 to obtain an estimate of the changes in emissions in Mexico City and the effectiveness of control strategies adopted during that time. Concentrations of PAN in 1997 reached a maximum of 34 ppb with an average daily maximum of 15 ppb. The PAN levels recorded in 2003 were quite different, with an average daily maximum of 3 ppb. This dramatic reduction in PAN levels observed in 2003 indicate that reactive hydrocarbon emissions have been reduced in the city due to controls on olefins in liquefied petroleum gas (LPG) and also due to the significant number of newer vehicles with catalytic converters that have replaced older higher emission vehicles. In contrast, black/elemental carbon levels were similar in 1997 and 2003 indicating little improvement likely due to the lack of controls on diesel vehicles in the city. Thus, while air quality and ozone production have improved, Mexico City and other megacities continue to be a major

  18. Comparison of measurements of peroxyacyl nitrates and primary carbonaceous aerosol concentrations in Mexico City determined in 1997 and 2003

    Directory of Open Access Journals (Sweden)

    N. A. Marley

    2007-01-01

    Full Text Available Peroxyacetyl nitrate (PAN concentrations in ambient air can be a good indicator of air quality and the effectiveness of control strategies for reducing ozone levels in urban areas. As PAN is formed by the oxidation of reactive hydrocarbons in the presence of nitrogen dioxide (NO2, it is a direct measure of the peroxyacyl radical levels produced from reactive organic emissions in the urban air shed. Carbon soot, known as black carbon or elemental carbon, is a primary atmospheric aerosol species and is a good indicator of the levels of combustion emissions, particularly from diesel engines, in major cities. Mexico City is the second largest megacity in the world and has long suffered from poor air quality. Reported here are atmospheric measurements of PAN and black carbon obtained in Mexico City during the Mexico Megacity 2003 field study. These results are compared with measurements obtained earlier during the Investigación sobre Materia Particulada y Deterioro Atmosférico – Aerosol and Visibility Research (IMADA-AVER campaign in 1997 to obtain an estimate of the changes in emissions in Mexico City and the effectiveness of control strategies adopted during that time. Concentrations of PAN in 1997 reached a maximum of 34 ppb with an average daily maximum of 15 ppb. The PAN levels recorded in 2003 were quite different, with an average daily maximum of 3 ppb. This dramatic reduction in PAN levels observed in 2003 indicate that reactive hydrocarbon emissions have been reduced in the city due to controls on olefins in liquefied petroleum gas (LPG and also due to the significant number of newer vehicles with catalytic converters that have replaced older higher emission vehicles. In contrast, black/elemental carbon levels were similar in 1997 and 2003 indicating little improvement likely due to the lack of controls on diesel vehicles in the city. Thus, while air quality and ozone production has improved, Mexico City and other

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

    Science.gov (United States)

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

    2014-12-01

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

  20. Characterization of high-resolution aerosol mass spectra of primary organic aerosol emissions from Chinese cooking and biomass burning

    Directory of Open Access Journals (Sweden)

    L.-Y. He

    2010-09-01

    Full Text Available Aerosol Mass Spectrometer (AMS has proved to be a powerful tool to measure submicron particulate composition with high time resolution. Factor analysis of mass spectra (MS collected worldwide by AMS demonstrates that submicron organic aerosol (OA is usually composed of several major components, such as oxygenated (OOA, hydrocarbon-like (HOA, biomass burning (BBOA, and other primary OA. In order to help interpretation of component MS from factor analysis of ambient OA datasets, AMS measurement of different primary sources is required for comparison. Such work, however, has been very scarce in the literature, especially for high resolution MS (HR-MS measurement, which performs improved characterization by separating the ions of different elemental compositions at each m/z in comparison with unit mass resolution MS (UMR-MS measurement. In this study, primary emissions from four types of Chinese cooking (CC and six types of biomass burning (BB were simulated systemically and measured using an Aerodyne High-Resolution Time-of-Flight AMS (HR-ToF-AMS. The MS of the CC emissions show high similarity with m/z 41 and m/z 55 being the highest signals; the MS of the BB emissions also show high similarity with m/z 29 and m/z 43 being the highest signals. The MS difference between the CC and BB emissions is much bigger than that between different CC (or BB types, especially for the HR-MS. The O/C ratio of OA ranges from 0.08 to 0.13 for the CC emissions while from 0.18 to 0.26 for the BB emissions. The ions of m/z 43, m/z 44, m/z 57, and m/z 60, usually used as tracer ions in AMS measurement, were examined for their HR-MS characteristics in the CC and BB emissions. Moreover, the MS of the CC and BB emissions are also used to compare with component MS from factor analysis of ambient OA datasets observed in China, as well as with other AMS measurements of primary sources in the literature. The MS

  1. South African night sky brightness during high aerosol epochs

    CERN Document Server

    Winkler, Hartmut; Marang, Fred

    2014-01-01

    Sky conditions in the remote, dry north-western interior of South Africa are now the subject of considerable interest in view of the imminent construction of numerous solar power plants in this area. Furthermore, the part of this region in which the core of the SKA is to be located (which includes SALT) has been declared an Astronomical Advantage Zone, for which sky brightness monitoring will now be mandatory. In this project we seek to characterise the sky brightness profile under a variety of atmospheric conditions. Key factors are of course the lunar phase and altitude, but in addition the sky brightness is also significantly affected by the atmospheric aerosol loading, as that influences light beam scattering. In this paper we chose to investigate the sky characteristics soon after the Mount Pinatubo volcanic eruption in 1991, which resulted in huge ash masses reaching the stratosphere (where they affected solar irradiance for several years). We re-reduced photometric sky measurements from the South Afric...

  2. Aerosol retrieval algorithm for the characterization of local aerosol using MODIS L1B data

    Science.gov (United States)

    Wahab, A. M.; Sarker, M. L. R.

    2014-02-01

    Atmospheric aerosol plays an important role in radiation budget, climate change, hydrology and visibility. However, it has immense effect on the air quality, especially in densely populated areas where high concentration of aerosol is associated with premature death and the decrease of life expectancy. Therefore, an accurate estimation of aerosol with spatial distribution is essential, and satellite data has increasingly been used to estimate aerosol optical depth (AOD). Aerosol product (AOD) from Moderate Resolution Imaging Spectroradiometer (MODIS) data is available at global scale but problems arise due to low spatial resolution, time-lag availability of AOD product as well as the use of generalized aerosol models in retrieval algorithm instead of local aerosol models. This study focuses on the aerosol retrieval algorithm for the characterization of local aerosol in Hong Kong for a long period of time (2006-2011) using high spatial resolution MODIS level 1B data (500 m resolution) and taking into account the local aerosol models. Two methods (dark dense vegetation and MODIS land surface reflectance product) were used for the estimation of the surface reflectance over land and Santa Barbara DISORT Radiative Transfer (SBDART) code was used to construct LUTs for calculating the aerosol reflectance as a function of AOD. Results indicate that AOD can be estimated at the local scale from high resolution MODIS data, and the obtained accuracy (ca. 87%) is very much comparable with the accuracy obtained from other studies (80%-95%) for AOD estimation.

  3. Fluorescence spectra and elastic scattering characteristics of atmospheric aerosol in Las Cruces, New Mexico, USA: Variability of concentrations and possible constituents and sources of particles in various spectral clusters

    Science.gov (United States)

    Pinnick, R. G.; Fernandez, E.; Rosen, J. M.; Hill, S. C.; Wang, Y.; Pan, Y. L.

    2013-02-01

    The UV-excited laser-induced-fluorescence (UV-LIF) spectra of single atmospheric particles and the three-band integrating-nephelometer elastic scattering of atmospheric aerosol were measured during four approximately 24-h periods on May 2007 in Las Cruces, New Mexico, USA. Aerosol scattering measurements in the nephelometer red channel (50-nm band centered at 700-nm) ranged from around 3-10 times the molecular (Rayleigh) scattering background. On average 22.8% of particles with size greater than about 1 μm diameter have fluorescence above a preset fluorescence threshold. A hierarchical cluster analysis indicates that most of the single-particle UV-LIF spectra fall into about 10 categories (spectral clusters) as found previously at other geographic sites (Pinnick et al., 2004; Pan et al., 2007). The clusters include spectra characteristic of various humic/fulvic acids, humic-like-substances (HULIS), chemically aged terpenes, fungal spores, polycyclic aromatic hydrocarbons, bacteria, cellulose/pollens, and mixtures of various organic carbon compounds. By far the most populated cluster category is similar to those of chemically aged terpenes/humic-materials; on average this population comprises about 62% of fluorescent particles. Clusters with spectra similar to that of some HULIS aerosol contain on average 10.0% of particles; those characteristic of some fungal spores (or perhaps mixtures of aromatic organic compounds) 8.4% of particles; bacteria-like spectra 1.6% of particles; and cellulose/pollen-like spectra 0.8% of particles. Measurements of fluorescent particles over relatively short (24 min) periods reveal that the concentrations of particles in the most populated clusters are highly correlated, suggesting that the particles populating them derive from the same region; these particles might be composed of crustal material coated with secondary organic carbon. On the other hand, concentrations of particles having cellulose-like spectra are generally

  4. Estimating marine aerosol particle volume and number from Maritime Aerosol Network data

    Directory of Open Access Journals (Sweden)

    A. M. Sayer

    2012-09-01

    Full Text Available As well as spectral aerosol optical depth (AOD, aerosol composition and concentration (number, volume, or mass are of interest for a variety of applications. However, remote sensing of these quantities is more difficult than for AOD, as it is more sensitive to assumptions relating to aerosol composition. This study uses spectral AOD measured on Maritime Aerosol Network (MAN cruises, with the additional constraint of a microphysical model for unpolluted maritime aerosol based on analysis of Aerosol Robotic Network (AERONET inversions, to estimate these quantities over open ocean. When the MAN data are subset to those likely to be comprised of maritime aerosol, number and volume concentrations obtained are physically reasonable. Attempts to estimate surface concentration from columnar abundance, however, are shown to be limited by uncertainties in vertical distribution. Columnar AOD at 550 nm and aerosol number for unpolluted maritime cases are also compared with Moderate Resolution Imaging Spectroradiometer (MODIS data, for both the present Collection 5.1 and forthcoming Collection 6. MODIS provides a best-fitting retrieval solution, as well as the average for several different solutions, with different aerosol microphysical models. The "average solution" MODIS dataset agrees more closely with MAN than the "best solution" dataset. Terra tends to retrieve lower aerosol number than MAN, and Aqua higher, linked with differences in the aerosol models commonly chosen. Collection 6 AOD is likely to agree more closely with MAN over open ocean than Collection 5.1. In situations where spectral AOD is measured accurately, and aerosol microphysical properties are reasonably well-constrained, estimates of aerosol number and volume using MAN or similar data would provide for a greater variety of potential comparisons with aerosol properties derived from satellite or chemistry transport model data. However, without accurate AOD data and prior knowledge of

  5. Examination of parameterizations for CCN number concentrations based on in-situ aerosol activation property measurements in the North China Plain

    Directory of Open Access Journals (Sweden)

    Z. Z. Deng

    2013-01-01

    Full Text Available Precise quantification of cloud condensation nuclei (CCN number concentrations is crucial for understanding aerosol indirect effect and characterizing this effect in models. An evaluation of various methods for CCN parameterization is carried out in this paper based on in-situ measurements of aerosol activation properties within HaChi (Haze in China project. Comparisons are made by closure studies between methods using CCN spectra, bulk activation ratios, cut-off diameters and size-resolved activation ratios. The estimation of CCN number concentrations by the method using aerosol activation curves, either averaged over a day or with diurnal variation, is found to be most satisfying and straightforward. This could be well expected since size-resolved activation ratios include information regarding the effects of size-resolved chemical composition and mixing state on aerosol activation properties. The method using the averages of critical diameters, which are inferred from measured CCN number concentrations and particle number size distribution, also provides a good prediction of CCN number concentrations. Based on comparisons of all these methods in this paper, it is recommended that CCN number concentrations be predicted using particle number size distribution with inferred critical diameters or size-resolved activation ratios.

  6. Organosulfates and organic acids in Arctic aerosols: Speciation, annual variation and concentration levels

    DEFF Research Database (Denmark)

    Hansen, Anne Maria Kaldal; Kristensen, Kasper; Nguyen, Quynh

    2014-01-01

    concentrations of organosulfates (47 +/- 14 ng m(-3)) and organic acids (11.5 +/- 4 ng m(-3)) were observed in January, February and March, contrary to considerably lower mean concentrations of organosulfates (2 +/- 3 ng m(3-)) and organic acids (2.2 +/- 1 ng m(-3)) observed during the rest of the year...... organosulfates - from both anthropogenic and biogenic precursors were in focus. A total of 11 organic acids (terpenylic acid, benzoic acid, phthalic acid, pinic acid, suberic acid, azelaic acid, adipic acid, pimelic acid, pinonic acid, diaterpenylic acid acetate and 3-methyl-1,2,3-butanetricarboxylic acid), 12....... At Zeppelin Mountain, organosulfate and organic acid concentrations remained relatively constant during most of the year at a mean concentration of 15 +/- 4 ng m(-3) and 3.9 +/- 1 ng m(-3), respectively. However during four weeks of spring, remarkably higher concentrations of total organosulfates (23-36 ng m...

  7. Three years of aerosol mass, black carbon and particle number concentrations at Montsec (southern~Pyrenees, 1570 m a.s.l.

    Directory of Open Access Journals (Sweden)

    A. Ripoll

    2013-10-01

    Full Text Available Time variation of mass particulate matter (PM1 and PM1−10, black carbon (BC and particle number (N concentrations at the high altitude site of Montsec (MSC in the southern Pyrenees was interpreted for the period 2010–2012. The MSC site registered higher PM10 (12 μg m−3 and N > 7 nm (2209 # cm−3 concentrations than those measured at other high altitude sites in central Europe (PM10: 3–9 μg m−3 and N: 634–2070 # cm−3. By contrast, BC concentrations at MSC (0.2 μg m−3 were equal or even lower than those measured at these European sites (0.2–0.4 μg m−3. These differences were attributed to the lower influence of anthropogenic emissions and to the higher relevance of Saharan dust transport and new particle formation (NPF processes at MSC. The different time variation of PM and BC concentrations compared with that of N suggests that these aerosol parameters were governed by diverse factors at MSC. Both PM and BC concentrations showed marked differences for different meteorological scenarios, with enhanced concentrations under North African outbreaks (PM1−10: 13 μg m−3, PM1: 8 μg m−3 and BC: 0.3 μg m−3 and low concentrations when Atlantic advections occurred (PM1−10: 5 μg m−3, PM1: 4 μg m−3 and BC: 0.1 μg m−3. Because of the contrasting origin of the air masses in the warmer seasons (spring and summer and in the colder seasons (autumn and winter, PM and BC concentrations showed a marked increase in summer, with a secondary maximum in early spring, and were at their lowest during winter. The maximum in the warmer seasons was attributed to long-range transport processes which mask the breezes and regional transport breaking the daily cycles of these pollutants. By contrast, PM and BC concentrations showed clear diurnal cycles with maxima at midday in the colder seasons. A statistically significant weekly variation was also obtained for the BC concentrations, displaying a progressive increase from Tuesday to

  8. Three years of aerosol mass, black carbon and particle number concentrations at Montsec (southern~Pyrenees, 1570 m a.s.l.)

    Science.gov (United States)

    Ripoll, A.; Pey, J.; Minguillón, M. C.; Pérez, N.; Pandolfi, M.; Querol, X.; Alastuey, A.

    2013-10-01

    Time variation of mass particulate matter (PM1 and PM1-10), black carbon (BC) and particle number (N) concentrations at the high altitude site of Montsec (MSC) in the southern Pyrenees was interpreted for the period 2010-2012. The MSC site registered higher PM10 (12 μg m-3) and N > 7 nm (2209 # cm-3) concentrations than those measured at other high altitude sites in central Europe (PM10: 3-9 μg m-3 and N: 634-2070 # cm-3). By contrast, BC concentrations at MSC (0.2 μg m-3) were equal or even lower than those measured at these European sites (0.2-0.4 μg m-3). These differences were attributed to the lower influence of anthropogenic emissions and to the higher relevance of Saharan dust transport and new particle formation (NPF) processes at MSC. The different time variation of PM and BC concentrations compared with that of N suggests that these aerosol parameters were governed by diverse factors at MSC. Both PM and BC concentrations showed marked differences for different meteorological scenarios, with enhanced concentrations under North African outbreaks (PM1-10: 13 μg m-3, PM1: 8 μg m-3 and BC: 0.3 μg m-3) and low concentrations when Atlantic advections occurred (PM1-10: 5 μg m-3, PM1: 4 μg m-3 and BC: 0.1 μg m-3). Because of the contrasting origin of the air masses in the warmer seasons (spring and summer) and in the colder seasons (autumn and winter), PM and BC concentrations showed a marked increase in summer, with a secondary maximum in early spring, and were at their lowest during winter. The maximum in the warmer seasons was attributed to long-range transport processes which mask the breezes and regional transport breaking the daily cycles of these pollutants. By contrast, PM and BC concentrations showed clear diurnal cycles with maxima at midday in the colder seasons. A statistically significant weekly variation was also obtained for the BC concentrations, displaying a progressive increase from Tuesday to Saturday, followed by a significant

  9. Physical chemistry of highly concentrated emulsions.

    Science.gov (United States)

    Foudazi, Reza; Qavi, Sahar; Masalova, Irina; Malkin, Alexander Ya

    2015-06-01

    This review explores the physics underlying the rheology of highly concentrated emulsions (HCEs) to determine the relationship between elasticity and HCE stability, and to consider whether it is possible to describe all physicochemical properties of HCEs on the basis of a unique physical approach. We define HCEs as emulsions with a volume fraction above the maximum closest packing fraction of monodisperse spheres, φm=0.74, even if droplets are not of polyhedron shape. The solid-like rheological behavior of HCEs is characterized by yield stress and elasticity, properties which depend on droplet polydispersity and which are affected by caging at volume fractions about the jamming concentration, φj. A bimodal size distribution in HCEs diminishes caging and facilitates droplet movement, resulting in HCEs with negligible yield stress and no plateau in storage modulus. Thermodynamic forces automatically move HCEs toward the lowest free energy state, but since interdroplet forces create local minimums - points beyond which free energy temporarily increases before it reaches the global minimum of the system - the free energy of HCEs will settle at a local minimum unless additional energy is added. Several attempts have been undertaken to predict the elasticity of HCEs. In many cases, the elastic modulus of HCEs is higher than the one predicted from classical models, which only take into account spatial repulsion (or simply interfacial energy). Improved models based on free energy calculation should be developed to consider the disjoining pressure and interfacial rheology in addition to spatial repulsion. The disjoining pressure and interfacial viscoelasticity, which result in the deviation of elasticity from the classical model, can be regarded as parameters for quantifying the stability of HCEs. Copyright © 2015 Elsevier B.V. All rights reserved.

  10. Impact of global climate change on ozone, particulate matter, and secondary organic aerosol concentrations in California: A model perturbation analysis

    Science.gov (United States)

    Horne, Jeremy R.; Dabdub, Donald

    2017-03-01

    Air quality simulations are performed to determine the impact of changes in future climate and emissions on regional air quality in the South Coast Air Basin (SoCAB) of California. The perturbation parameters considered in this study include (1) temperature, (2) absolute humidity, (3) biogenic VOC emissions due to temperature changes, and (4) boundary conditions. All parameters are first perturbed individually. In addition, the impact of simultaneously perturbing more than one parameter is analyzed. Air quality is simulated with meteorology representative of a summertime ozone pollution episode using both a baseline 2005 emissions inventory and a future emissions projection for the year 2023. Different locations within the modeling domain exhibit varying degrees of sensitivity to the perturbations considered. Afternoon domain wide average ozone concentrations are projected to increase by 13-18% as a result of changes in future climate and emissions. Afternoon increases at individual locations range from 10 to 36%. The change in afternoon particulate matter (PM) levels is a strong function of location in the basin, ranging from -7.1% to +4.7% when using 2005 emissions and -8.6% to +1.7% when using 2023 emissions. Afternoon secondary organic aerosol (SOA) concentrations for the entire domain are projected to decrease by over 15%, and the change in SOA levels is not a strong function of the emissions inventory utilized. Temperature increases play the dominant role in determining the overall impact on ozone, PM, and SOA concentrations in both the individual and combined perturbation scenarios.

  11. Comparison of concentrations of selected aerosol components estimated using the AERONET data set with those from continuous/semi-continuous measurements on the ground

    Science.gov (United States)

    Choi, Y.; Ghim, Y.

    2013-12-01

    A CIEMEL sunphotometer was operated in 2012 starting from March as a part of the DRAGON (Distributed Regional Aerosol Gridded Observation Networks) campaign. The site is Hankuk_UFS (Hankuk University of Foreign Studies; 37.02 °N, 127.16 °E, 167 m above sea level) located about 35 km southeast of downtown Seoul. We also measured inorganic ions using PILS (Particle-Into-Liquid Sampler, ADI 2081, Applikon) at intervals of 25 minutes in spring and winter and BC (black carbon) using MAAP (Multiangle Absorption Photometer, Model 5012, Thermo) at intervals of 10 minutes throughout the study period. Concentrations of major chemical components were estimated from effective real and imaginary refractory indices for a mixture assuming the Maxwell-Garnett mixing of four components such as mineral dust, organic and black carbons, and ammonium sulfate (as a surrogate of secondary ions) embedded in water host. We compare ammonium sulfate of column aerosols estimated from the refractive indices with secondary ions of surface aerosols from PILS and BC of column aerosols estimated from the refractive indices with that of surface aerosols from MAAP. Since the measurement intervals are different between sunphotometer and surface instruments, we compare the concentrations when the measurement time coincides within 5 minutes.

  12. The challenge of measuring sulfuric acid aerosols: number concentration and size evaluation using a condensation particle counter (CPC) and an electrical low pressure impactor (ELPI+)

    NARCIS (Netherlands)

    Brachert, L.; Mertens, J.; Khakharia, P.M.; Schaber, K.

    2014-01-01

    In this study, two different methods for the measurement of the sulfuric acid aerosol which is formed in wet flue gas cleaning processes have been investigated. The condensation particle counter (UFCPC, PALAS GmbH) provides information about the number concentration. With the electrical low pressure

  13. Changes in concentration, composition and source contribution of atmospheric organic aerosols by shifting coal to natural gas in Urumqi

    Science.gov (United States)

    Ren, Yanqin; Wang, Gehui; Wu, Can; Wang, Jiayuan; Li, Jianjun; Zhang, Lu; Han, Yanni; Liu, Lang; Cao, Cong; Cao, Junji; He, Qing; Liu, Xinchun

    2017-01-01

    Size-segregated aerosols were collected in Urumqi, a megacity in northwest China, during two heating seasons, i.e., before (heating season І: January-March 2012) and after (heating season II: January-March 2014) the project "shifting coal to natural gas", and determined for n-alkanes, PAHs and oxygenated PAHs to investigate the impact of replacement of coal by natural gas on organic aerosols in the urban atmosphere. Our results showed that compared to those in heating season I concentrations of n-alkanes, PAHs and OPAHs decreased by 74%, 74% and 82% in heating season II, respectively. Source apportionment analysis suggested that coal combustion, traffic emission and biomass burning are the major sources of the determined organics during the heating seasons in Urumqi. Traffic emission is the main source for n-alkanes in the city. Coal combustion is the dominant source of PAHs and OPAHs in heating season І, but traffic emission becomes their major source in heating season ІI. Relative contributions of coal combustion to n-alkanes, PAHs and OPAHs in Urumqi decreased from 21 to 75% in heating season I to 4.0-21% in heating season II due to the replacement of coal with natural gas for house heating. Health risk assessment further indicated that compared with that in heating season I the number of lung cancer related to PAHs exposure in Urumqi decreased by 73% during heating season II due to the project implementation. Our results suggest that replacing coal by clean energy sources for house heating will significantly mitigate air pollution and improve human health in China.

  14. Impacts of alternative fuels in aviation on microphysical aerosol properties and predicted ice nuclei concentration at aircraft cruise altitude

    Science.gov (United States)

    Weinzierl, B.; D'Ascoli, E.; Sauer, D. N.; Kim, J.; Scheibe, M.; Schlager, H.; Moore, R.; Anderson, B. E.; Ullrich, R.; Mohler, O.; Hoose, C.

    2015-12-01

    In the past decades air traffic has been substantially growing affecting air quality and climate. According to the International Civil Aviation Authority (ICAO), in the next few years world passenger and freight traffic is expected to increase annually by 6-7% and 4-5%, respectively. One possibility to reduce aviation impacts on the atmosphere and climate might be the replacement of fossil fuels by alternative fuels. However, so far the effects of alternative fuels on particle emissions from aircraft engines and their ability to form contrails remain uncertain. To study the effects of alternative fuels on particle emissions and the formation of contrails, the Alternative Fuel Effects on Contrails and Cruise Emissions (ACCESS) field experiment was conducted in California. In May 2014, the DLR Falcon 20 and the NASA HU-25 jet aircraft were instrumented with an extended aerosol and trace gas payload probing different types of fuels including JP-8 and JP-8 blended with HEFA (Hydroprocessed Esters and Fatty Acids) while the NASA DC8 aircraft acted as the source aircraft for ACCESS-2. Emission measurements were taken in the DC8 exhaust plumes at aircraft cruise level between 9-12 km altitude and at distances between 50 m and 20 km behind the DC8 engines. Here, we will present results from the ACCESS-2 aerosol measurements which show a 30-60% reduction of the non-volatile (mainly black carbon) particle number concentration in the aircraft exhaust for the HEFA-blend compared to conventional JP-8 fuel. Size-resolved particle emission indices show the largest reductions for larger particle sizes suggesting that the HEFA blend contains fewer and smaller black carbon particles. We will combine the airborne measurements with a parameterization of deposition nucleation developed during a number of ice nucleation experiments at the AIDA chamber in Karlsruhe and discuss the impact of alternative fuels on the abundance of potential ice nuclei at cruise conditions.

  15. Fast airborne aerosol size and chemistry measurements above Mexico City and Central Mexico during the MILAGRO campaign

    National Research Council Canada - National Science Library

    DeCarlo, P. F; Dunlea, E. J; Kimmel, J. R; Aiken, A. C; Sueper, D; Crounse, J; Wennberg, P. O; Emmons, L; Shinozuka, Y; Clarke, A; Zhou, J; Tomlinson, J; Collins, D. R; Knapp, D; Weinheimer, A. J; Montzka, D. D; Campos, T; Jimenez, J. L

    2008-01-01

    The concentration, size, and composition of non-refractory submicron aerosol (NR-PM 1 ) was measured over Mexico City and central Mexico with a High-Resolution Time-of-Flight Aerosol Mass Spectrometer...

  16. Effects of seed aerosols on the growth of secondary organic aerosols from the photooxidation of toluene

    Institute of Scientific and Technical Information of China (English)

    HAO Li-qing; WANG Zhen-ya; HUANG Ming-qiang; FANG Li; ZHANG Wei-jun

    2007-01-01

    Hydroxyl radical (·OH)-initiated photooxidation reaction of toluene was carried out in a self-made smog chamber. Four individual seed aerosols such as ammonium sulfate, ammonium nitrate, sodium silicate and calcium chloride, were introduced into the chamber to assess their influence on the growth of secondary organic aerosols (SOA). It was found that the low concentration of seed aerosols might lead to high concentration of SOA particles. Seed aerosols would promote rates of SOA formation at the start of the reaction and inhibit its formation rate with prolonging the reaction time. In the case of cv. 9000 pt/cm3 seed aerosol load, the addition of sodium silicate induced a same effect on the SOA formation as ammonium nitrate. The influence of the four individual seed aerosols on the generation of SOA increased in the order of calcium chloride>sodium silicate and ammonium nitrate> ammonium sulfate.

  17. Aerosol radiative effect in UV, VIS, NIR, and SW spectra under haze and high-humidity urban conditions

    Science.gov (United States)

    Zhang, Ming; Ma, Yingying; Gong, Wei; Wang, Lunche; Xia, Xiangao; Che, Huizheng; Hu, Bo; Liu, Boming

    2017-10-01

    Aerosol properties derived from sun-photometric observations at Wuhan during a haze period were analyzed and used as input in a radiative transfer model to calculate the aerosol radiative effect (ARE) in ultraviolet (UV), visible (VIS), near-infrared (NIR), and shortwave (SW) spectra. The results showed that the aerosol optical depth (AOD) at 440 nm increased from 0.32 under clear-air conditions to 0.85 during common haze and 1.39 during severe haze. An unusual inverse relationship was found between the Ångström exponent (AE) and AOD during the haze period at Wuhan. Under high-humidity conditions, the fine-mode median radius of aerosols increased from 0.113 μm to approximately 0.2-0.5 μm as a result of hygroscopic growth, which led to increases in the AOD and decreases in the AE simultaneously. These changes were responsible for the inverse relationship between AE and AOD at Wuhan. The surface ARE in the UV (AREUV), VIS (AREVIS), NIR (ARENIR), and SW (ARESW) spectra changed from -4.46, -25.37, -12.15, and -41.99 W/m2 under clear-air conditions to -9.48, -53.96, -29.81, and -93.25 W/m2 during common hazy days and -12.89, -80.16, -55.17, and -148.22 W/m2 during severe hazy days, respectively, and the percentages of AREUV, AREVIS, and ARENIR in ARESW changed from 11%, 61%, and 28%-9%, 54%, and 37%, respectively. Meanwhile, the ARE efficiencies (REE) in SW varied from -206.5 W/m2 under clear-air conditions to -152.94 W/m2 during the common haze period and -131.47 W/m2 during the severe haze period. The smallest decreasing rate of the REE in NIR was associated with the increase of ARENIR. The weakened REE values were related to the strong forward scattering and weak backward scattering of fine aerosol particles with increasing size resulting from hygroscopic growth, while the variation of the single scattering albedo showed less impact. Source region analysis by back trajectories and the concentration weighted trajectory (CWT) method showed that black carbon came

  18. High formation of secondary organic aerosol from the photo-oxidation of toluene

    Directory of Open Access Journals (Sweden)

    L. Hildebrandt

    2009-01-01

    Full Text Available Toluene and other aromatics have long been viewed as the dominant anthropogenic secondary organic aerosol (SOA precursors, but the SOA mass yields from toluene reported in previous studies vary widely. Experiments conducted in the Carnegie Mellon University environmental chamber to study SOA formation from the photo-oxidation of toluene show significantly larger SOA production than parameterizations employed in current air-quality models. Aerosol mass yields depend on experimental conditions: yields are higher under higher UV intensity, under low-NOx conditions and at lower temperatures. The extent of oxidation of the aerosol also varies with experimental conditions, consistent with ongoing, progressive photochemical aging of the toluene SOA. Measurements using a thermodenuder system suggest that the aerosol formed under high- and low-NOx conditions is semi-volatile. These results suggest that SOA formation from toluene depends strongly on ambient conditions. An approximate parameterization is proposed for use in air-quality models until a more thorough treatment accounting for the dynamic nature of this system becomes available.

  19. High formation of secondary organic aerosol from the photo-oxidation of toluene

    Directory of Open Access Journals (Sweden)

    L. Hildebrandt

    2009-05-01

    Full Text Available Toluene and other aromatics have long been viewed as the dominant anthropogenic secondary organic aerosol (SOA precursors, but the SOA mass yields from toluene reported in previous studies vary widely. Experiments conducted in the Carnegie Mellon University environmental chamber to study SOA formation from the photo-oxidation of toluene show significantly larger SOA production than parameterizations employed in current air-quality models. Aerosol mass yields depend on experimental conditions: yields are higher under higher UV intensity, under low-NOx conditions and at lower temperatures. The extent of oxidation of the aerosol also varies with experimental conditions, consistent with ongoing, progressive photochemical aging of the toluene SOA. Measurements using a thermodenuder system suggest that the aerosol formed under high- and low-NOx conditions is semi-volatile. These results suggest that SOA formation from toluene depends strongly on ambient conditions. An approximate parameterization is proposed for use in air-quality models until a more thorough treatment accounting for the dynamic nature of this system becomes available.

  20. Manipulating API and AOD data to distinguish transportation of aerosol at high altitude in Penang, Malaysia

    Science.gov (United States)

    Tan, F.; Lim, H. S.; Abdullah, K.; Yoon, T. L.; Matjafri, M. Z.; Holben, B.

    2014-02-01

    Air pollution index (API) is an index commonly used in Malaysia to determine the air quality level. It is a ground truth data measurement which is unable to unambiguously quantify air quality level at higher atmosphere. On the other hand, aerosol optical depth (AOD) from AERONET data obtained using sun photometer provides reading of the air quality for a column of atmosphere from ground surface. We first determine the quantitative correlation between the API and AOD data collected in Penang, Malaysia, between January - September, 2012, using two independent methods, one based on regression analysis and the other interpolation. Our purpose is to establish a systematic numerical procedure to determine whether aerosol transported in high altitude from other location has occurred. Two independent methods for establishing the quantitative relationship between the API and AOD data were used as a way to facilitate the verification of our approach. In our method, data from southwest monsoon period (August to September) were used as "calibration dataset" to establish the quantitative correlation between the AOD and API data. The established calibrated coefficients is then used to predict the AOD of other months, which are then compared against the data actually measured. Discrepancy between the predicted and measured AOD data can then be interpreted as an indication of whether the atmosphere at high altitude is polluted by aerosol transported from other location. If the predicted AOD is much larger than that measured, back trajectory analysis was applied to identify the aerosol transported source. This procedure is very helpful to investigate the aerosol transportation and distribution patterns during monsoon and non monsoon periods.

  1. 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.

  2. 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.

  3. Observed high-altitude warming and snow cover retreat over Tibet and the Himalayas enhanced by black carbon aerosols

    Science.gov (United States)

    Xu, Y.; Ramanathan, V.; Washington, W. M.

    2016-02-01

    Himalayan mountain glaciers and the snowpack over the Tibetan Plateau provide the headwater of several major rivers in Asia. In situ observations of snow cover extent since the 1960s suggest that the snowpack in the region have retreated significantly, accompanied by a surface warming of 2-2.5 °C observed over the peak altitudes (5000 m). Using a high-resolution ocean-atmosphere global climate model and an observationally constrained black carbon (BC) aerosol forcing, we attribute the observed altitude dependence of the warming trends as well as the spatial pattern of reductions in snow depths and snow cover extent to various anthropogenic factors. At the Tibetan Plateau altitudes, the increase in atmospheric CO2 concentration exerted a warming of 1.7 °C, BC 1.3 °C where as cooling aerosols cause about 0.7 °C cooling, bringing the net simulated warming consistent with the anomalously large observed warming. We therefore conclude that BC together with CO2 has contributed to the snow retreat trends. In particular, BC increase is the major factor in the strong elevation dependence of the observed surface warming. The atmospheric warming by BC as well as its surface darkening of snow is coupled with the positive snow albedo feedbacks to account for the disproportionately large role of BC in high-elevation regions. These findings reveal that BC impact needs to be properly accounted for in future regional climate projections, in particular on high-altitude cryosphere.

  4. The European aerosol budget in 2006

    Directory of Open Access Journals (Sweden)

    J. M. J. Aan de Brugh

    2011-02-01

    Full Text Available This paper presents the aerosol budget over Europe in 2006 calculated with the global transport model TM5 coupled to the size-resolved aerosol module M7. Comparison with ground observations indicates that the model reproduces the observed concentrations quite well with an expected slight underestimation of PM10 due to missing emissions (e.g. resuspension. We model that a little less than half of the anthropogenic aerosols emitted in Europe are exported and the rest is removed by deposition. The anthropogenic aerosols are removed mostly by rain (95% and only 5% is removed by dry deposition. For the larger natural aerosols, especially sea salt, a larger fraction is removed by dry processes (sea salt: 70%, mineral dust: 35%. We model transport of aerosols in the jet stream in the higher atmosphere and an import of Sahara dust from the south at high altitudes. Comparison with optical measurements shows that the model reproduces the Ångström parameter very well, which indicates a correct simulation of the aerosol size distribution. However, we underestimate the aerosol optical depth. Because the surface concentrations are close to the observations, the shortage of aerosol in the model is probably at higher altitudes. We show that the discrepancies are mainly caused by an overestimation of wet-removal rates. To match the observations, the wet-removal rates have to be scaled down by a factor of about 5. In that case the modelled ground-level concentrations of sulphate and sea salt increase by 50% (which deteriorates the match, while other components stay roughly the same. Finally, it is shown that in particular events, improved fire emission estimates may significantly improve the ability of the model to simulate the aerosol optical depth. We stress that discrepancies in aerosol models can be adequately analysed if all models would provide (regional aerosol budgets, as presented in the current study.

  5. Eddy covariance measurements with high-resolution time-of-flight aerosol mass spectrometry: a new approach to chemically resolved aerosol fluxes

    Directory of Open Access Journals (Sweden)

    D. K. Farmer

    2011-06-01

    Full Text Available Although laboratory studies show that biogenic volatile organic compounds (VOCs yield substantial secondary organic aerosol (SOA, production of biogenic SOA as indicated by upward fluxes has not been conclusively observed over forests. Further, while aerosols are known to deposit to surfaces, few techniques exist to provide chemically-resolved particle deposition fluxes. To better constrain aerosol sources and sinks, we have developed a new technique to directly measure fluxes of chemically-resolved submicron aerosols using the high-resolution time-of-flight aerosol mass spectrometer (HR-AMS in a new, fast eddy covariance mode. This approach takes advantage of the instrument's ability to quantitatively identify both organic and inorganic components, including ammonium, sulphate and nitrate, at a temporal resolution of several Hz. The new approach has been successfully deployed over a temperate ponderosa pine plantation in California during the BEARPEX-2007 campaign, providing both total and chemically resolved non-refractory (NR PM1 fluxes. Average deposition velocities for total NR-PM1 aerosol at noon were 2.05 ± 0.04 mm s−1. Using a high resolution measurement of the NH2+ and NH3+ fragments, we demonstrate the first eddy covariance flux measurements of particulate ammonium, which show a noon-time deposition velocity of 1.9 ± 0.7 mm s−1 and are dominated by deposition of ammonium sulphate.

  6. Seasonal variations in high time-resolved chemical compositions, sources, and evolution of atmospheric submicron aerosols in the megacity Beijing

    Science.gov (United States)

    Hu, Wei; Hu, Min; Hu, Wei-Wei; Zheng, Jing; Chen, Chen; Wu, Yusheng; Guo, Song

    2017-08-01

    A severe regional haze problem in the megacity Beijing and surrounding areas, caused by fast formation and growth of fine particles, has attracted much attention in recent years. In order to investigate the secondary formation and aging process of urban aerosols, four intensive campaigns were conducted in four seasons between March 2012 and March 2013 at an urban site in Beijing (116.31° E, 37.99° N). An Aerodyne high-resolution time-of-flight aerosol mass spectrometry (HR-ToF-AMS) was deployed to measure non-refractory chemical components of submicron particulate matter (NR-PM1). The average mass concentrations of PM1 (NR-PM1+black carbon) were 45.1 ± 45.8, 37.5 ± 31.0, 41.3 ± 42.7, and 81.7 ± 72.4 µg m-3 in spring, summer, autumn, and winter, respectively. Organic aerosol (OA) was the most abundant component in PM1, accounting for 31, 33, 44, and 36 % seasonally, and secondary inorganic aerosol (SNA, sum of sulfate, nitrate, and ammonium) accounted for 59, 57, 43, and 55 % of PM1 correspondingly. Based on the application of positive matrix factorization (PMF), the sources of OA were obtained, including the primary ones of hydrocarbon-like (HOA), cooking (COA), biomass burning OA (BBOA) and coal combustion OA (CCOA), and secondary component oxygenated OA (OOA). OOA, which can be split into more-oxidized (MO-OOA) and less-oxidized OOA (LO-OOA), accounted for 49, 69, 47, and 50 % in four seasons, respectively. Totally, the fraction of secondary components (OOA+SNA) contributed about 60-80 % to PM1, suggesting that secondary formation played an important role in the PM pollution in Beijing, and primary sources were also non-negligible. The evolution process of OA in different seasons was investigated with multiple metrics and tools. The average carbon oxidation states and other metrics show that the oxidation state of OA was the highest in summer, probably due to both strong photochemical and aqueous-phase oxidations. It was indicated by the good correlations

  7. Aerosol isotopic ammonium signatures over the remote Atlantic Ocean

    Science.gov (United States)

    Lin, C. T.; Jickells, T. D.; Baker, A. R.; Marca, A.; Johnson, M. T.

    2016-05-01

    We report aerosol ammonium 15N signatures for samples collected from research cruises on the South Atlantic and Caribbean using a new high sensitivity method. We confirm a pattern of isotopic signals from generally light (δ15N -5 to -10‰), for aerosols with very low (ocean, to generally heavier values (δ15N +5 to +10‰), for aerosols collected in temperate and tropical latitudes and with higher ammonium concentrations (>2 nmol m-3). We discuss whether this reflects a mixing of aerosols from two end-members (polluted continental and remote marine emissions), or isotopic fractionation during aerosol transport.

  8. Impact of atmospheric boundary layer depth variability and wind reversal on the diurnal variability of aerosol concentration at a valley site

    Energy Technology Data Exchange (ETDEWEB)

    Pal, S., E-mail: sp5hd@Virginia.EDU; Lee, T.R.; Phelps, S.; De Wekker, S.F.J.

    2014-10-15

    The development of the atmospheric boundary layer (ABL) plays a key role in affecting the variability of atmospheric constituents such as aerosols, greenhouse gases, water vapor, and ozone. In general, the concentration of any tracers within the ABL varies due to the changes in the mixing volume (i.e. ABL depth). In this study, we investigate the impact on the near-surface aerosol concentration in a valley site of 1) the boundary layer dilution due to vertical mixing and 2) changes in the wind patterns. We use a data set obtained during a 10-day field campaign in which a number of remote sensing and in-situ instruments were deployed, including a ground-based aerosol lidar system for monitoring of the ABL top height (z{sub i}), a particle counter to determine the number concentration of aerosol particles at eight different size ranges, and tower-based standard meteorological instruments. Results show a clearly visible decreasing trend of the mean daytime z{sub i} from 2900 m AGL (above ground level) to 2200 m AGL during a three-day period which resulted in increased near-surface pollutant concentrations. An inverse relationship exists between the z{sub i} and the fine fraction (0.3–0.7 μm) accumulation mode particles (AMP) on some days due to the dilution effect in a well-mixed ABL. These days are characterized by the absence of daytime upvalley winds and the presence of northwesterly synoptic-driven winds. In contrast, on the days with an onset of an upvalley wind circulation after the morning transition, the wind-driven local transport mechanism outweighs the ABL-dilution effect in determining the variability of AMP concentration. The interplay between the ABL depth evolution and the onset of the upvalley wind during the morning transition period significantly governs the air quality in a valley and could be an important component in the studies of mountain meteorology and air quality. - Highlights: • Role of atmospheric boundary layer depth on particle

  9. High-Temperature, High-Concentration Solar Thermoelectric Generators

    Science.gov (United States)

    Warren, Emily; Baranowski, Lauryn; Olsen, Michele; Ndione, Paul; Netter, Judy; Goodrich, Alan; Gray, Matthew; Parilla, Philip; Ginley, David; Toberer, Eric

    2014-03-01

    Solar thermoelectric generators (STEGs) powered with concentrated solar energy have potential for use as primary energy converters or as topping-cycles for more conventional concentrated solar power (CSP) technologies. Modeling based on current record modules from JPL suggests thermoelectric efficiencies of 18 % could be experimentally expected with a temperature gradient of 1000 - 100°C. Integrating these state-of-the-art TEGs with a concentrating solar receiver requires simultaneous optimization of optical, thermal, and thermoelectric systems. This talk will discuss the modeling, design, and experimental testing of STEG devices under concentrated sunlight. We have developed a model that combines thermal circuit modeling with optical ray tracing to design selective absorber coatings and cavities to minimize radiation losses from the system. We have fabricated selective absorber coatings and demonstrated that these selective absorber films can minimize blackbody radiation losses at high temperature and are stable after thermal cycling to 1000°C. On-sun testing of STEG devices and thermal simulators is ongoing and preliminary results will be discussed.

  10. Measured In Situ Atmospheric Ambient Aerosol Size-Distributions, Particle Concentrations, and Turbulence Data for RSA TA-6 Test Range, Redstone Arsenal, AL, April-May 2015

    Science.gov (United States)

    2015-09-01

    Concentrations, and Turbulence Data for RSA TA-6 Test Range, Redstone Arsenal , AL, April–May 2015 by Kristan Gurton, Stephanie Cunningham, and...Aerosol Size-Distributions, Particle Concentrations, and Turbulence Data for RSA TA-6 Test Range, Redstone Arsenal , AL, April–May 2015 by Kristan...Redstone Arsenal , AL Approved for public release; distribution unlimited. ii REPORT DOCUMENTATION PAGE Form Approved OMB No. 0704-0188

  11. Production of high concentrations of yeast

    Energy Technology Data Exchange (ETDEWEB)

    1981-11-10

    A microbe is aerobically cultured using O/sub 2/ or a gas rich in O/sub 2/. The grown cells are washed, concentrated and a portion of the cells used as a seed culture. Thus, Saccharomyces cerevisiae (bakers' yeast) was cultured in a jar fermentor by flow down system maintaining the dissolved O/sub 2/ at 2-5 mg/L; volume of the initial medium containing 30% glucose was 350 mL and the initial washed cell concentration was 50 g dry cells/L. After 12 hours of cultivation, the volume of the medium increased to 750 mL and the cell concentration rose to 102 g dry cells/L; the yield was 49% with respect to glucose. The cells were washed and the cultivation was repeated by use of the washed cells; cell concentration reached 105 g dry cells/L.

  12. 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.

  13. Study of particle size distribution and formation mechanism of radioactive aerosols generated in high-energy neutron fields

    CERN Document Server

    Endo, A; Noguchi, H; Tanaka, S; Iida, T; Furuichi, S; Kanda, Y; Oki, Y

    2003-01-01

    The size distributions of sup 3 sup 8 Cl, sup 3 sup 9 Cl, sup 8 sup 2 Br and sup 8 sup 4 Br aerosols generated by irradiations of argon and krypton gases containing di-octyl phthalate (DOP) aerosols with 45 MeV and 65 MeV quasi-monoenergetic neutrons were measured in order to study the formation mechanism of radioactive particles in high energy radiation fields. The effects of the size distribution of the radioactive aerosols on the size of the added DOP aerosols, the energy of the neutrons and the kinds of nuclides were studied. The observed size distributions of the radioactive particles were explained by attachment of the radioactive atoms generated by the neutron-induced reactions to the DOP aerosols. (author)

  14. Results and code predictions for ABCOVE (aerosol behavior code validation and evaluation) aerosol code validation with low concentration NaOH and NaI aerosol: CSTF test AB7

    Energy Technology Data Exchange (ETDEWEB)

    Hilliard, R.K.; McCormack, J.D.; Muhlestein, L.D.

    1985-10-01

    A program for aerosol behavior validation and evaluation (ABCOVE) has been developed in accordance with the LMFBR Safety Program Plan. The ABCOVE program is a cooperative effort between the USDOE, the USNRC, and their contractor organizations currently involved in aerosol code development, testing or application. The third large-scale test in the ABCOVE program, AB7, was performed in the 850-m/sup 3/ CSTF vessel with a two-species test aerosol. The test conditions involved the release of a simulated fission product aerosol, NaI, into the containment atmosphere after the end of a small sodium pool fire. Four organizations made pretest predictions of aerosol behavior using five computer codes. Two of the codes (QUICKM and CONTAIN) were discrete, multiple species codes, while three (HAA-3, HAA-4, and HAARM-3) were log-normal codes which assume uniform coagglomeration of different aerosol species. Detailed test results are presented and compared with the code predictions for eight key aerosol behavior parameters. 11 refs., 44 figs., 35 tabs.

  15. Emission of submicron aerosol particles in cement kilns: Total concentration and size distribution.

    Science.gov (United States)

    Rotatori, Mauro; Mosca, Silvia; Guerriero, Ettore; Febo, Antonio; Giusto, Marco; Montagnoli, Mauro; Bianchini, Massimo; Ferrero, Renato

    2015-01-01

    Cement plants are responsible for particle and gaseous emissions into the atmosphere. With respect to particle emission, the greater part of is in the range from 0.05 to 5.0 µm in diameter. In the last years attention was paid to submicron particles, but there is a lack of available data on the emission from stationary sources. In this paper, concentration and size distribution of particles emitted from four cement kilns, in relationship to operational conditions (especially the use of alternative fuel to coal) of the clinker process are reported. Experimental campaigns were carried out by measuring particles concentration and size distribution at the stack of four cement plants through condensation particle counter (CPC) and scanning mobility particle sizer spectrometer (SMPS). Average total particle number concentrations were between 2000 and 4000 particles/cm³, about 8-10 times lower that those found in the corresponding surrounding areas. As for size distribution, for all the investigated plants it is stable with a unimodal distribution (120-150 nm), independent from the fuel used.

  16. Simultaneous aerosol measurements of unusual aerosol enhancement in troposphere over Syowa Station, Antarctica

    Directory of Open Access Journals (Sweden)

    K. Hara

    2013-10-01

    Full Text Available Unusual aerosol enhancement is often observed at Syowa Station, Antarctica during winter through spring. Simultaneous aerosol measurements near the surface and in the upper atmosphere were conducted twice using a ground-based optical particle counter, a balloon-borne optical particle counter, and micro-pulse LIDAR (MPL in August and September 2012. During 13–15 August, aerosol enhancement occurred immediately after a storm condition. A high backscatter ratio and aerosol concentrations were observed from the surface to ca. 2.5 km over Syowa Station. Clouds appeared occasionally at the top of aerosol-enhanced layer during the episode. Aerosol enhancement was terminated on 15 August by strong winds caused by a cyclone's approach. In the second case on 5–7 September, aerosol number concentrations in Dp > 0.3 μm near the surface reached > 104 L−1 at about 15:00 UT on 5 September in spite of calm wind conditions, whereas MPL measurement exhibited aerosols were enhanced at about 04:00 UT at 1000–1500 m above Syowa Station. The aerosol enhancement occurred near the surface–ca. 4 km. In both cases, air masses with high aerosol enhancement below 2.5–3 km were transported mostly from the boundary layer over the sea-ice area. In addition, air masses at 3–4 km in the second case came from the boundary layer over the open-sea area. This air mass history strongly suggests that dispersion of sea-salt particles from the sea-ice surface contributes considerably to the aerosol enhancement in the lower free troposphere (about 3 km and that the release of sea-salt particles from the ocean surface engenders high aerosol concentrations in the free troposphere (3–4 km.

  17. Horizontally staggered lightguide solar concentrator with lateral displacement tracking for high concentration applications.

    Science.gov (United States)

    Ma, Hongcai; Wu, Lin

    2015-07-10

    We present the design of a horizontally staggered lightguide solar concentrator with lateral displacement tracking for high concentration applications. This solar concentrator consists of an array of telecentric primary concentrators, a horizontally staggered lightguide layer, and a vertically tapered lightguide layer. The primary concentrator is realized by two plano-aspheric lenses with lateral movement and maintains a high F-number over an angle range of ±23.5°. The results of the simulations show that the solar concentrator achieves a high concentration ratio of 500× with ±0.5° of acceptance angle by a single-axis tracker and dual lateral translation stages.

  18. Climatology of Aerosol Optical Properties in Southern Africa

    Science.gov (United States)

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

    2011-01-01

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

  19. Climatology of Aerosol Optical Properties in Southern Africa

    Science.gov (United States)

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

    2011-01-01

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

  20. The effect of dry and wet deposition of condensable vapors on secondary organic aerosols concentrations over the continental US

    Directory of Open Access Journals (Sweden)

    C. Knote

    2015-01-01

    Full Text Available The effect of dry and wet deposition of semi-volatile organic compounds (SVOCs in the gas phase on the concentrations of secondary organic aerosol (SOA is reassessed using recently derived water solubility information. The water solubility of SVOCs was implemented as a function of their volatility distribution within the WRF-Chem regional chemistry transport model, and simulations were carried out over the continental United States for the year 2010. Results show that including dry and wet removal of gas-phase SVOCs reduces annual average surface concentrations of anthropogenic and biogenic SOA by 48 and 63% respectively over the continental US. Dry deposition of gas-phase SVOCs is found to be more effective than wet deposition in reducing SOA concentrations (−40 vs. −8% for anthropogenics, and −52 vs. −11% for biogenics. Reductions for biogenic SOA are found to be higher due to the higher water solubility of biogenic SVOCs. The majority of the total mass of SVOC + SOA is actually deposited via the gas phase (61% for anthropogenics and 76% for biogenics. Results are sensitive to assumptions made in the dry deposition scheme, but gas-phase deposition of SVOCs remains crucial even under conservative estimates. Considering reactivity of gas-phase SVOCs in the dry deposition scheme was found to be negligible. Further sensitivity studies where we reduce the volatility of organic matter show that consideration of gas-phase SVOC removal still reduces average SOA concentrations by 31% on average. We consider this a lower bound for the effect of gas-phase SVOC removal on SOA concentrations. A saturation effect is observed for Henry's law constants above 108 M atm−1, suggesting an upper bound of reductions in surface level SOA concentrations by 60% through removal of gas-phase SVOCs. Other models that do not consider dry and wet removal of gas-phase SVOCs would hence overestimate SOA concentrations by roughly 50%. Assumptions about the water

  1. Impacts of Stabilized Criegee Intermediates, surface uptake processes and higher aromatic secondary organic aerosol yields on predicted PM2.5 concentrations in the Mexico City Metropolitan Zone

    Science.gov (United States)

    Ying, Qi; Cureño, Iris V.; Chen, Gang; Ali, Sajjad; Zhang, Hongliang; Malloy, Meagan; Bravo, Humberto A.; Sosa, Rodolfo

    2014-09-01

    The Community Multiscale Air Quality Model (CMAQ) with the SAPRC-99 gas phase photochemical mechanism and the AERO5 aerosol module was applied to model gases and particulate matter (PM) concentrations in the Mexico City Metropolitan Zone (MCMZ) and the surrounding regions for March 2006 using the official 2006 emission inventories, along with emissions from biogenic sources, biomass burning, windblown dust, the Tula Industrial Complex and the Popocatépetl volcano. The base case model was capable of reproducing the observed hourly concentrations of O3 and attaining CO, NO2 and NOx performance similar to previous modeling studies. Although the base case model performance of hourly PM2.5 and PM10 meets the model performance criteria, under-prediction of high PM2.5 concentrations in late morning indicates that secondary PM, such as sulfate and secondary organic aerosol (SOA), might be under-predicted. Several potential pathways to increase SOA and secondary sulfate were investigated, including Stabilized Criegee Intermediates (SCIs) from ozonolysis reactions of unsaturated hydrocarbons and their reactions with SO2, the reactive uptake processes of SO2, glyoxal and methylglyoxal on particle surface and higher SOA formation due to higher mass yields of aromatic SOA precursors. Averaging over the entire episode, the glyoxal and methylglyoxal reactive uptake and higher aromatics SOA yields contribute to ∼0.9 μg m-3 and ∼1.25 μg m-3 of SOA, respectively. Episode average SOA in the MCMZ reaches ∼3 μg m-3. The SCI pathway increases PM2.5 sulfate by 0.2-0.4 μg m-3 or approximately 10-15%. The relative amount of sulfate increase due to SCI agrees with previous studies in summer eastern US. Surface SO2 uptake significantly increases sulfate concentration in MCMZ by 1-3 μg m-3 or approximately 50-60%. The higher SOA and sulfate leads to improved PM2.5 and PM10 model performance.

  2. First lidar measurements of water vapor and aerosols from a high-altitude aircraft

    Science.gov (United States)

    Browell, Edward V.; Ismail, Syed

    1995-01-01

    Water vapor plays an important role in many atmospheric processes related to radiation, climate change, atmospheric dynamics, meteorology, the global hydrologic cycle, and atmospheric chemistry, and yet our knowledge of the global distribution of water vapor is very limited. The differential absorption lidar (DIAL) technique has the potential of providing needed high resolution water vapor measurements from aircraft and from space, and the Lidar Atmospheric Sensing Experiment (LASE) is a key step in the development of this capability. The LASE instrument is the first fully engineered, autonomous DIAL system, and it is designed to operate from a high-altitude aircraft (ER-2) and to make water vapor and aerosol profile measurements across the troposphere. The LASE system was flown from the NASA Wallops Flight Facility in a series of engineering flights during September 1994. This paper discusses the characteristics of the LASE system and presents the first LASE measurements of water vapor and aerosol profiles.

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

    Science.gov (United States)

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

    2010-01-01

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

  4. Investigation of a New Electrostatic Sampler for Concentrating Biological and Non-Biological Aerosol Particles

    OpenAIRE

    Roux, Jean-Maxime; Kaspari, Oliver; Heinrich, Renate; Hanschmann, Nicole; Grunow, Roland

    2013-01-01

    The detection of airborne pathogens is becoming a subject of great concern in modern day society. Recent studies have shown that electrostatic samplers are suitable for collecting microorganisms as well as preserving their viability. In most of these studies, flow rates were lower than 12.5 L/min or required a concentration stage to increase the flow rate to 100 L/min. In the present study, a single stage electrostatic sampler was developed for an efficient collection of microorganisms at 100...

  5. Modeling of metallic aerosol formation in a multicomponent system at high temperatures using a discrete-sectional model. Appendix 7

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1997-02-01

    A multicomponent discrete-sectional model was used to simulate the fate of lead in a high temperature system. The results show the ability of the developed model to simulate metallic aerosol systems at high temperatures. The PbO reaction and nucleation rate can be determined by comparing the simulations and the experimental data. Condensation on SiO{sub 2} particle surfaces is found important for removing the PbO vapor. The value of the accommodation factor that is applied to account for nonidealities in the condensation process are determined. The differences between the nanosized particles and the bulk particles are elucidated. The use of such a model helped to understand the effects of various mechanisms in determining the metal oxide vapor concentration profile and in establishing the ultimate particle size distribution.

  6. Molecular composition and volatility of isoprene photochemical oxidation secondary organic aerosol under low- and high-NOx conditions

    Science.gov (United States)

    D'Ambro, Emma L.; Lee, Ben H.; Liu, Jiumeng; Shilling, John E.; Gaston, Cassandra J.; Lopez-Hilfiker, Felipe D.; Schobesberger, Siegfried; Zaveri, Rahul A.; Mohr, Claudia; Lutz, Anna; Zhang, Zhenfa; Gold, Avram; Surratt, Jason D.; Rivera-Rios, Jean C.; Keutsch, Frank N.; Thornton, Joel A.

    2017-01-01

    We present measurements of secondary organic aerosol (SOA) formation from isoprene photochemical oxidation in an environmental simulation chamber at a variety of oxidant conditions and using dry neutral seed particles to suppress acid-catalyzed multiphase chemistry. A high-resolution time-of-flight chemical ionization mass spectrometer (HR-ToF-CIMS) utilizing iodide-adduct ionization coupled to the Filter Inlet for Gases and Aerosols (FIGAERO) allowed for simultaneous online sampling of the gas and particle composition. Under high-HO2 and low-NO conditions, highly oxygenated (O : C ≥ 1) C5 compounds were major components (˜ 50 %) of SOA. The SOA composition and effective volatility evolved both as a function of time and as a function of input NO concentrations. Organic nitrates increased in both the gas and particle phases as input NO increased, but the dominant non-nitrate particle-phase components monotonically decreased. We use comparisons of measured and predicted gas-particle partitioning of individual components to assess the validity of literature-based group-contribution methods for estimating saturation vapor concentrations. While there is evidence for equilibrium partitioning being achieved on the chamber residence timescale (5.2 h) for some individual components, significant errors in group-contribution methods are revealed. In addition, > 30 % of the SOA mass, detected as low-molecular-weight semivolatile compounds, cannot be reconciled with equilibrium partitioning. These compounds desorb from the FIGAERO at unexpectedly high temperatures given their molecular composition, which is indicative of thermal decomposition of effectively lower-volatility components such as larger molecular weight oligomers.

  7. Effect of number concentration of soot and H2SO4 on aerosol based emissions from a post combustion capture plant

    NARCIS (Netherlands)

    Khakharia, P.M.; Brachert, L.; Schaber, K.; Huizinga, A.; Vlugt, T.; Mertens, J.; Schallert, B.; Goetheer, E.L.V.

    2013-01-01

    It is known that the use of volatile solvents for a post combustion capture process can lead to emission of the solvent due to their high vapour pressure. More recently, the issue of emission due to the formation of aerosols has been observed at different pilot plants. Therefore, it is of high impor

  8. Fluctuations of the Concentration of Cs-137 Aerosol in Chernobyl,Fukushima and Kawasaki

    Science.gov (United States)

    Ota, Yohei; Hatano, Yuko; Okada, Yukiko; Hirose, Katsumi

    2017-04-01

    Statistical analysis is applied to a time series of the airborne concentration of Cs-137. In order to extract fractal characteristics of the fluctuations, we employed the Hurst analysis. Interestingly, the Hurst index is around 1/3, which is common to the Chernobyl data, Fukushima data, and Kawasaki data. The Kawasaki data is measured by the Tokyo City University, located at 40km south to Tokyo. We proposed a stochastic differential equation, based on an advection equation with winds fluctuating probabilistically. The averaged solution of the equation is compared with measured data. We found that the index of the power of the time is -4/3, which is common to the three cases, Chernobyl, Fukushima and Kawasaki.

  9. A semiempirical correlation between enthalpy of vaporization and saturation concentration for organic aerosol.

    Science.gov (United States)

    Epstein, Scott A; Riipinen, Ilona; Donahue, Neil M

    2010-01-15

    To model the temperature-induced partitioning of semivolatile organics in laboratory experiments or atmospheric models, one must know the appropriate heats of vaporization. Current treatments typically assume a constant value of the heat of vaporization or else use specific values from a small set of surrogate compounds. With published experimental vapor-pressure data from over 800 organic compounds, we have developed a semiempirical correlation between the saturation concentration (C*, microg m(-3)) and the heat of vaporization (deltaH(VAP), kJ mol(-1)) for organics in the volatility basis set. Near room temperature, deltaH(VAP) = -11 log(10)C(300)(*) + 129. Knowledge of the relationship between C* and deltaH(VAP) constrains a free parameter in thermodenuder data analysis. A thermodenuder model using our deltaH(VAP) values agrees well with thermal behavior observed in laboratory experiments.

  10. On-line analysis of urban particulate matter focusing on elevated wintertime aerosol concentrations.

    Science.gov (United States)

    Tan, Phillip V; Evans, Greg J; Tsai, Julia; Owega, Sandy; Fila, Michael S; Malpica, Oscar; Brook, Jeffrey R

    2002-08-15

    A 10-day winter sampling campaign was conducted in downtown Toronto for particulate matter (PM) air pollution in the fine (z peaks 58(C3HeN)+, 86(C5H2N)+, and nitrates, increased in number concentration while Ca and hydrocarbon particle classes concurrently decreased. On another day, sulfates were found to have increased significantly. The third event was only 4 h in duration and exhibited an increase in the number of submicron-sized K/hydrocarbons and sulfate-containing particles. In this last event, the hydrocarbons and a K to Fe ratio enrichment indicated there was likely a contribution from a combustion source. This work offers some of the first insights into single particle size and chemistry in a cold winter climate.

  11. Synthesis of Trace Gas and Aerosol Observations and Evaluation of Modelled Short-lived Climate Pollutants Across the Pan-Eurasian High Latitudes

    Science.gov (United States)

    Arnold, S.; Nieminen, T.

    2015-12-01

    Model calculations suggest that changes in short-lived climate pollutants (SLCPs) such as ozone and aerosol may have contributed significantly to rapid Arctic warming over the past century. Arctic tropospheric budgets of SLCPs are impacted by long-range transport of trace gases and aerosols from Europe, Asia and N. America, but also by local sources such as gas flaring, shipping and boreal fires. Recently, the POLARCAT Model Intercomparison Project (POLMIP) showed that significant model biases persist through the depth of the European and North American high latitude troposphere in modelled trace-gas abundances. Evaluation of models over the Siberian high latitudes is challenging due to a severe paucity of available observations, despite the potential importance of this region as a route for European pollution export to the Arctic. Despite the existence of a number of limited datasets, which could be used for model evaluation in this region, until now no effort has been made to synthesise and exploit these observations to evaluate modelled abundances of SLCPs such as tropospheric ozone & aerosol. In this presentation, we will show evaluation of simulated aerosol, tropospheric ozone, and precursor species in several global chemical transport models, using a synthesis of available surface, aircraft and satellite observations over the high latitude pan-Eurasian region. We use models and observations to investigate source regions contributing to remote Siberian SLCP abundances over the annual cycle, and show substantial biases in simulated aerosol and trace gas concentrations that are consistent across a suite of different models. These comparisons constitute the first multi-model evaluation of tropospheric composition in the pan-Eurasin region using observations from across the broad region. Finally, we use the model simulations to determine optimum locations for the development of future monitoring activities in high latitude Eurasia with an aim of better

  12. High performance liquid chromatography study of complex oxygenated alkane mixtures from organic aerosols

    Science.gov (United States)

    Kalafut-Pettibone, Alicia J.; Klems, Joseph P.; McGivern, W. Sean

    2013-05-01

    The composition of secondary organic aerosol particles is of primary importance both in identifying particle sources and in determining physical parameters, such as cloud condensation nucleus propensity. Further, measurements of composition are valuable in determining the chemistry of formation and aging. In this work, we describe the application of a recently-developed derivatization technique to a complex synthetic organic aerosol derived from the photolysis of 1-iodooctane. The technique utilizes high-performance liquid chromatography (HPLC) coupled to both ultravioletvisible (UV/VIS) spectroscopy and tandem mass spectrometry (MS-MS) to determine the overall distribution of hydroxyl (OH), non-acid carbonyl (C=O), and carboxylic acid (COOH) moieties as well as the specific identities of chromatographically separated products. This composition data will then be used to constrain models of the particle formation mechanisms.

  13. Molecular dynamics simulation of the local concentration and structure in multicomponent aerosol nanoparticles under atmospheric conditions.

    Science.gov (United States)

    Karadima, Katerina S; Mavrantzas, Vlasis G; Pandis, Spyros N

    2017-06-28

    Molecular dynamics (MD) simulations were employed to investigate the local structure and local concentration in atmospheric nanoparticles consisting of an organic compound (cis-pinonic acid or n-C30H62), sulfate and ammonium ions, and water. Simulations in the isothermal-isobaric (NPT) statistical ensemble under atmospheric conditions with a prespecified number of molecules of the abovementioned compounds led to the formation of a nanoparticle. Calculations of the density profiles of all the chemical species in the nanoparticle, the corresponding radial pair distribution functions, and their mobility inside the nanoparticle revealed strong interactions developing between sulfate and ammonium ions. However, sulfate and ammonium ions prefer to populate the central part of the nanoparticle under the simulated conditions, whereas organic molecules like to reside at its outer surface. Sulfate and ammonium ions were practically immobile; in contrast, the organic molecules exhibited appreciable mobility at the outer surface of the nanoparticle. When the organic compound was a normal alkane (e.g. n-C30H62), a well-organized (crystalline-like) phase was rapidly formed at the free surface of the nanoparticle and remained separate from the rest of the species.

  14. Assessment of the global impact of aerosols on tropospheric oxidants

    Science.gov (United States)

    Tie, Xuexi; Madronich, Sasha; Walters, Stacy; Edwards, David P.; Ginoux, Paul; Mahowald, Natalie; Zhang, Renyi; Lou, Chao; Brasseur, Guy

    2005-02-01

    We present here a fully coupled global aerosol and chemistry model for the troposphere. The model is used to assess the interactions between aerosols and chemical oxidants in the troposphere, including (1) the conversion from gas-phase oxidants into the condensed phase during the formation of aerosols, (2) the heterogeneous reactions occurring on the surface of aerosols, and (3) the effect of aerosols on ultraviolet radiation and photolysis rates. The present study uses the global three-dimensional chemical/transport model, Model for Ozone and Related Chemical Tracers, version 2 (MOZART-2), in which aerosols are coupled with the model. The model accounts for the presence of sulfate, soot, primary organic carbon, ammonium nitrate, secondary organic carbon, sea salt, and mineral dust particles. The simulated global distributions of the aerosols are analyzed and evaluated using satellite measurements (Moderate-Resolution Imaging Spectroradiometer (MODIS)) and surface measurements. The results suggest that in northern continental regions the tropospheric aerosol loading is highest in Europe, North America, and east Asia. Sulfate, organic carbon, black carbon, and ammonium nitrate are major contributions for the high aerosol loading in these regions. Aerosol loading is also high in the Amazon and in Africa. In these areas the aerosols consist primarily of organic carbon and black carbon. Over the southern high-latitude ocean (around 60°S), high concentrations of sea-salt aerosol are predicted. The concentration of mineral dust is highest over the Sahara and, as a result of transport, spread out into adjacent regions. The model and MODIS show similar geographical distributions of aerosol particles. However, the model overestimates the sulfate and carbonaceous aerosol in the eastern United States, Europe, and east Asia. In the region where aerosol loading is high, aerosols have important impacts on tropospheric ozone and other oxidants. The model suggests that

  15. Optimized sparse-particle aerosol representations for modeling cloud-aerosol interactions

    Science.gov (United States)

    Fierce, Laura; McGraw, Robert

    2016-04-01

    Sparse representations of atmospheric aerosols are needed for efficient regional- and global-scale chemical transport models. Here we introduce a new framework for representing aerosol distributions, based on the method of moments. Given a set of moment constraints, we show how linear programming can be used to identify collections of sparse particles that approximately maximize distributional entropy. The collections of sparse particles derived from this approach reproduce CCN activity of the exact model aerosol distributions with high accuracy. Additionally, the linear programming techniques described in this study can be used to bound key aerosol properties, such as the number concentration of CCN. Unlike the commonly used sparse representations, such as modal and sectional schemes, the maximum-entropy moment-based approach is not constrained to pre-determined size bins or assumed distribution shapes. This study is a first step toward a new aerosol simulation scheme that will track multivariate aerosol distributions with sufficient computational efficiency for large-scale simulations.

  16. Atmospheric hydrogen peroxide and organic hydroperoxides during PRIDE-PRD'06, China: their concentration, formation mechanism and contribution to secondary aerosols

    Directory of Open Access Journals (Sweden)

    W. Hua

    2008-11-01

    detected in this region can account for the production of hydroperoxides, while the moderate level of NOx suppressed the formation of hydroperoxides. High concentrations of hydroperoxides were detected in samples of rainwater collected in a heavy shower on 25 July when a typhoon passed through, indicating that a considerable mixing ratio of hydroperoxides, particularly MHP, resided above the boundary layer, which might be transported on a regional scale and further influence the redistribution of HOx and ROx radicals. It was found that hydroperoxides, in particular H2O2, play an important role in the formation of secondary sulfate in the aerosol phase, where the heterogeneous reaction might contribute substantially. A negative correlation between hydroperoxides and water-soluble organic compounds (WSOC, a considerable fraction of the secondary organic aerosol (SOA, was observed, possibly providing field evidence for the importance of hydroperoxides in the formation of SOA found in previous laboratory studies. We suggest that hydroperoxides act as an important link between sulfate and organic aerosols, which needs further study and should be considered in current atmospheric models.

  17. Overview of atmospheric aerosol studies in Malaysia: Known and unknown

    Science.gov (United States)

    Kanniah, Kasturi Devi; Kaskaoutis, Dimitris G.; San Lim, Hwee; Latif, Mohd Talib; Kamarul Zaman, Nurul Amalin Fatihah; Liew, Juneng

    2016-12-01

    Atmospheric aerosols particularly those originated from anthropogenic sources can affect human health, air quality and the regional climate system of Southeast Asia (SEA). Population growth, and rapid urbanization associated with economic development in the SEA countries including Malaysia have resulted in high aerosol concentrations. Moreover, transboundary smoke plumes add more aerosols to the atmosphere in Malaysia. Nevertheless, the aerosol monitoring networks and/or field studies and research campaigns investigating the various aerosol properties are not so widespread over Malaysia. In the present work, we summarize and discuss the results of previous studies that investigated the aerosol properties over Malaysia by means of various instrumentation and techniques, focusing on the use of remote sensing data to examine atmospheric aerosols. Furthermore, we identify gaps in this research field and recommend further studies to bridge these knowledge gaps. More specifically gaps are identified in (i) monitoring aerosol loading and composition over urban areas, (ii) examining the influence of dust, (iii) assessing radiative effects of aerosols, (iv) measuring and modelling fine particles and (v) quantifying the contribution of long range transport of aerosols. Such studies are crucial for understanding the optical, physical and chemical properties of aerosols and their spatio-temporal characteristics over the region, which are useful for modelling and prediction of aerosols' effects on air quality and climate system.

  18. Dominant aerosol processes during high-pollution episodes over Greater Tokyo

    CERN Document Server

    Sartelet, Karine; Sportisse, Bruno

    2007-01-01

    This paper studies two high-pollution episodes over Greater Tokyo: 9 and 10 December 1999, and 31 July and 1 August 2001. Results obtained with the chemistry-transport model (CTM) Polair3D are compared to measurements of inorganic PM2.5. To understand to which extent the aerosol processes modeled in Polair3D impact simulated inorganic PM2.5, Polair3D is run with different options in the aerosol module, e.g. with/without heterogeneous reactions. To quantify the impact of processes outside the aerosol module, simulations are also done with another CTM (CMAQ). In the winter episode, sulfate is mostly impacted by condensation, coagulation, long-range transport, and deposition to a lesser extent. In the summer episode, the effect of long-range transport largely dominates. The impact of condensation/evaporation is dominant for ammonium, nitrate and chloride in both episodes. However, the impact of the thermodynamic equilibrium assumption is limited. The impact of heterogeneous reactions is large for nitrate and amm...

  19. Generalized high-spectral-resolution lidar technique with a multimode laser for aerosol remote sensing.

    Science.gov (United States)

    Cheng, Zhongtao; Liu, Dong; Zhang, Yupeng; Liu, Chong; Bai, Jian; Wang, Dan; Wang, Nanchao; Zhou, Yudi; Luo, Jing; Yang, Yongying; Shen, Yibing; Su, Lin; Yang, Liming

    2017-01-23

    High-spectral-resolution lidar (HSRL) is a powerful tool for atmospheric aerosol remote sensing. The current HSRL technique often requires a single longitudinal mode laser as the transmitter to accomplish the spectral discrimination of the aerosol and molecular scattering conveniently. However, single-mode laser is cumbersome and has very strict requirements for ambient stability, making the HSRL instrument not so robust in many cases. In this paper, a new HSRL concept, called generalized HSRL technique with a multimode laser (MML-gHSRL), is proposed, which can work using a multimode laser. The MML-gHSRL takes advantage of the period characteristic of the spectral function of the interferometric spectral discrimination filter (ISDF) thoroughly. By matching the free spectral range of the ISDF with the mode interval of the multimode laser, fine spectral discrimination for the lidar return from each longitudinal mode can be realized. Two common ISDFs, i.e., the Fabry-Perot interferometer (FPI) and field-widened Michelson interferometer (FWMI), are introduced to develop the MML-gHSRL, and their performance is quantitatively analyzed and compared. The MML-gHSRL is a natural but significant generalization for the current HSRL technique based on the IDSF. It is potential that this technique would be a good entrance to future HSRL developments, especially in airborne and satellite-borne aerosol remote sensing applications.

  20. Characterization of Cooking-Related Aerosols

    Science.gov (United States)

    Niedziela, R. F.; Blanc, L. E.

    2010-12-01

    The temperatures at which food is cooked are usually high enough to drive oils and other organic compounds out of materials which are being prepared for consumption. As these compounds move away from the hot cooking surface and into the atmosphere, they can participate in chemical reactions or condense to form particles. Given the high concentration of cooking in urban areas, cooking-related aerosols likely contribute to the overall amount of particulate matter on a local scale. Reported here are results for the mid-infrared optical characterization of aerosols formed during the cooking of several meat and vegetable samples in an inert atmosphere. The samples were heated in a novel aerosol generator that is designed to collect particles formed immediately above the cooking surface and inject them into a laminar aerosol flow cell. Preliminary results for the chemical processing of cooking-related aerosols in synthetic air will also be presented.

  1. Building a Sectional Aerosol Model in CAM5

    Science.gov (United States)

    Yu, P.; Toon, O. B.

    2013-12-01

    Aerosols are widely distributed around the globe. In the current study I use a sectional aerosol microphysics model (CARMA) coupled with the NCAR global climate model, CAM5, to simulate the spatial-temporal distribution of various types of aerosols including organics, black carbon, sulfate, sea salt and dust. Organics and black carbon surface concentrations are simulated within ~50% over the U.S, and Europe compared with observations; the amount of modeled sulfate and organics are equal in UTLS region as observed by the Pre-AVE field campaign; aerosol extinction in the UTLS observed by SAGEII can be explained by secondary organic aerosols combined with sulfate aerosol. For treating secondary organic aerosols, the volatility-basis-set method improves the budget at surface level relative to the traditional two-product partitioning method; black carbon global budget is largely improved especially in high latitudes by introducing new emission database.

  2. 40 CFR Table F-6 to Subpart F of... - Estimated Mass Concentration Measurement of PM2.5 for Idealized Fine Aerosol Size Distribution

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 5 2010-07-01 2010-07-01 false Estimated Mass Concentration Measurement of PM2.5 for Idealized Fine Aerosol Size Distribution F Table F-6 to Subpart F of Part 53... Equivalent Methods for PM2.5 Pt. 53, Subpt. F, Table F-6 Table F-6 to Subpart F of Part 53—Estimated Mass...

  3. 40 CFR Table F-5 to Subpart F of... - Estimated Mass Concentration Measurement of PM2.5 for Idealized “Typical” Coarse Aerosol Size...

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 5 2010-07-01 2010-07-01 false Estimated Mass Concentration Measurement of PM2.5 for Idealized âTypicalâ Coarse Aerosol Size Distribution F Table F-5 to Subpart F of Part... of Class II Equivalent Methods for PM2.5 Pt. 53, Subpt. F, Table F-5 Table F-5 to Subpart F of Part...

  4. 40 CFR Table F-4 to Subpart F of... - Estimated Mass Concentration Measurement of PM2.5 for Idealized Coarse Aerosol Size Distribution

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 5 2010-07-01 2010-07-01 false Estimated Mass Concentration Measurement of PM2.5 for Idealized Coarse Aerosol Size Distribution F Table F-4 to Subpart F of Part 53... Equivalent Methods for PM2.5 Pt. 53, Subpt. F, Table F-4 Table F-4 to Subpart F of Part 53—Estimated Mass...

  5. An episode of extremely high PM concentrations over Central Europe caused by dust emitted over the southern Ukraine

    Directory of Open Access Journals (Sweden)

    W. Birmili

    2007-08-01

    Full Text Available On 24 March 2007, the atmosphere over Central Europe was affected by an episode of exceptionally high mass concentrations of aerosol particles, most likely caused by a dust storm in the Southern Ukraine on the preceding day. At ground-based measurement stations in Slovakia, the Czech Republic, Poland and Germany PM10 mass concentrations rose to values between 200 and 1400 μg m−3. An evaluation of PM10 measurements from 360 monitoring stations showed that the dust cloud advanced along a narrow corridor at speeds of up to 70 km h−1. According to lidar observations over Leipzig, Germany, the high aerosol concentrations were confined to a homogeneous boundary layer of 1800 m height. The wavelength dependence of light extinction using both lidar and sun photometer measurements suggested the dominance of coarse particles during the main event. At a wavelength of 532 nm, relatively high volume extinction coefficients (300–400 Mm−1 and a particle optical depth of 0.65 was observed. In-situ measurements with an aerodynamic particle sizer at Melpitz, Germany, confirmed the presence of a coarse particle mode with a mode diameter >2 μm, whose maximum concentration coincided with that of PM10. A chemical particle analysis confirmed the dominance of non-volatile and insoluble matter in the coarse mode as well as high enrichments of Ti and Fe, which are characteristic of soil dust. A combination of back trajectory calculations and satellite images allowed to identify the dust source with confidence: On 23 March 2007, large amounts of dust were emitted from dried-out farmlands in the southern Ukraine, facilitated by wind gusts up to 100 km h−1. The unusual vertical stability and confined height of this dust layer as well as the rapid transport under dry conditions led to the conservation of high aerosol mass concentrations along the transect and thus to the extraordinary

  6. A review of atmospheric aerosol measurements

    Science.gov (United States)

    McMurry, Peter H.

    carbon mass concentration is beset by difficulties including the unknown extent of evaporative losses during sampling, adsorption of gas-phase organic compounds onto sampling substrates, and the unknown relationship between carbon mass and mass of the particulate organics. The development of improved methodologies for such measurements should be a high priority for the future. Mass spectrometers that measure the composition of individual particles have recently been developed. It is not clear that these instruments will provide quantitative information on species mass concentrations, and more work is needed to routinely interpret the vast quantities of data generated during field sampling. Nevertheless, these instruments substantially expand the range of atmospheric aerosol issues that can be explored experimentally. These instruments represent the most significant advance in aerosol instrumentation in recent years.

  7. Application of WRF/Chem-MADRID and WRF/Polyphemus in Europe – Part 2: Evaluation of chemical concentrations, sensitivity simulations, and aerosol-meteorology interactions

    Directory of Open Access Journals (Sweden)

    C. Seigneur

    2013-02-01

    Full Text Available An offline-coupled model (WRF/Polyphemus and an online-coupled model (WRF/Chem-MADRID are applied to simulate air quality in July 2001 at horizontal grid resolutions of 0.5° and 0.125° over western Europe. The model performance is evaluated against available surface and satellite observations. The two models simulate different concentrations in terms of domainwide performance statistics, spatial distribution, temporal variations, and column abundance. WRF/Chem-MADRID at 0.5° gives higher values than WRF/Polyphemus for the domainwide mean and over polluted regions in central and southern Europe for all surface concentrations and column variables except for TOR. Compared with observations, WRF/Polyphemus gives better statistical performance for daily HNO3, SO2, and NO2 a