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Sample records for absorbing aerosol species

  1. Light Absorbing Aerosols in Mexico City

    NASA Astrophysics Data System (ADS)

    Marley, N. A.; Kelley, K. L.; Kilaparty, P. S.; Gaffney, J. S.

    2008-12-01

    The direct effects of aerosol radiative forcing has been identified by the IPCC as a major uncertainty in climate modeling. The DOE Megacity Aerosol Experiment-Mexico City (MAX-Mex), as part of the MILAGRO study in March of 2006, was undertaken to reduce these uncertainties by characterization of the optical, chemical, and physical properties of atmospheric aerosols emitted from this megacity environment. Aerosol samples collected during this study using quartz filters were characterized in the uv-visible-infrared by using surface spectroscopic techniques. These included the use of an integrating sphere approach combined with the use of Kubelka-Munk theory to obtain aerosol absorption spectra. In past work black carbon has been assumed to be the only major absorbing species in atmospheric aerosols with an broad band spectral profile that follows a simple inverse wavelength dependence. Recent work has also identified a number of other absorbing species that can also add to the overall aerosol absorption. These include primary organics from biomass and trash burning and secondary organic aerosols including nitrated PAHs and humic-like substances, or HULIS. By using surface diffuse reflection spectroscopy we have also obtained spectra in the infrared that indicate significant IR absorption in the atmospheric window-region. These data will be presented and compared to spectra of model compounds that allow for evaluation of the potential importance of these species in adding strength to the direct radiative forcing of atmospheric aerosols. This work was supported by the Office of Science (BER), U.S. Department of Energy, Grant No. DE-FG02-07ER64327 as part of the Atmospheric Science Program.

  2. Applications of UV Scattering and Absorbing Aerosol Indices

    NASA Astrophysics Data System (ADS)

    Penning de Vries, M.; Beirle, S.; Wagner, T.

    2009-04-01

    Aerosols cause a substantial amount of radiative forcing, but quantifying this amount is difficult: determining aerosol concentrations in the atmosphere and, especially, characterizing their (optical) properties, has proved to be quite a challenge. A good way to monitor aerosol characteristics on a global scale is to perform satellite remote sensing. Most satellite aerosol retrieval algorithms are based on fitting of aerosol-induced changes in earth reflectance, which are usually subtle and have a smooth wavelength dependence. In such algorithms certain aerosol models are assumed, where optical parameters such as single scattering albedo, asymmetry parameter and size parameter (or Angstrom exponent) are defined. Another, semi-quantitative technique for detecting aerosols is the calculation of UV Aerosol Indices (UVAI). The Absorbing and Scattering Aerosol Indices detect "UV-absorbing" aerosols (most notably mineral dust, black and brown carbon particles) and "scattering" aerosols (sulfate and secondary organic aerosol particles), respectively. UVAI are essentially a measure of the contrast between two wavelengths in the UV range. The advantages of UVAI are: they can be determined in the presence of clouds, they are rather insensitive to surface type, and they are very sensitive to aerosols. The Absorbing Aerosol Index (AAI) has been in use for over a decade, and the Scattering Aerosol Index (SAI) was recently introduced by our group. Whereas the AAI is mainly used to detect desert dust and biomass burning plumes, the SAI can be used to study regions with high concentrations of non-absorbing aerosols, either anthropogenic (e.g. sulfate aerosols in eastern China) or biogenic (e.g. secondary organic aerosols formed from VOCs emitted by plants). Here we will present our recent UVAI results from SCIAMACHY: we will discuss the seasonal trend of SAI, and correlate our UVAI data with other datasets such as trace gases (HCHO, NO2, CO) and fire counts from the (A

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

    NASA Astrophysics Data System (ADS)

    Randles, C. A.; Ramaswamy, V.

    2008-11-01

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

  4. Sensitivity of scattering and absorbing aerosol direct radiative forcing to physical climate factors

    NASA Astrophysics Data System (ADS)

    Ocko, Ilissa B.; Ramaswamy, V.; Ginoux, Paul; Ming, Yi; Horowitz, Larry W.

    2012-10-01

    The direct radiative forcing of the climate system includes effects due to scattering and absorbing aerosols. This study explores how important physical climate characteristics contribute to the magnitudes of the direct radiative forcings (DRF) from anthropogenic sulfate, black carbon, and organic carbon. For this purpose, we employ the GFDL CM2.1 global climate model, which has reasonable aerosol concentrations and reconstruction of twentieth-century climate change. Sulfate and carbonaceous aerosols constitute the most important anthropogenic aerosol perturbations to the climate system and provide striking contrasts between primarily scattering (sulfate and organic carbon) and primarily absorbing (black carbon) species. The quantitative roles of cloud coverage, surface albedo, and relative humidity in governing the sign and magnitude of all-sky top-of-atmosphere (TOA) forcings are examined. Clouds reduce the global mean sulfate TOA DRF by almost 50%, reduce the global mean organic carbon TOA DRF by more than 30%, and increase the global mean black carbon TOA DRF by almost 80%. Sulfate forcing is increased by over 50% as a result of hygroscopic growth, while high-albedo surfaces are found to have only a minor (less than 10%) impact on all global mean forcings. Although the radiative forcing magnitudes are subject to uncertainties in the state of mixing of the aerosol species, it is clear that fundamental physical climate characteristics play a large role in governing aerosol direct radiative forcing magnitudes.

  5. Interaction of absorbing aerosols with high relative humidity

    NASA Astrophysics Data System (ADS)

    Flores, M.; Bluvshtein, N.; Abo Riziq, A.; Borrmann, S.; Rudich, Y.

    2011-12-01

    One of the major uncertainties in the understanding of Earth's climate system is the interaction between solar radiation and aerosols in the atmosphere. This interaction is dependent on the physical and chemical properties of the aerosols and on the wavelength of the incident light. Aerosols exposed to high humidity areas will change their chemical, physical, and optical properties. To model hydrated aerosols, atmospheric chemistry models use the volume weighted mixing rule to predict the complex refractive index (RI) of aerosols when they interact with high relative humidity areas, and, in general, assume homogeneous mixing. The validity of these assumptions is explored. The extinction coefficient and growth factor of humidified aerosols, at 80% and 90% RH, and at 532 nm and 355 nm wavelengths was measured for size-selected aerosols of ammonium sulfate, peat (a lightly absorbing humic-like substance proxy), nigrosine (a black dye to model highly absorbing substances), and a mixture of AS and nigrosine. The ratio of the humidified extinction coefficients to the dry (fRHext(%RH,Dry)) is explored. The measured fRHext(%RH,Dry) is compared to theoretical calculations based on Mie theory, and using the measured 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. Moreover, the differences between assuming a core-shell structure or a homogeneous mixing of the substances is examined. We found slightly linear to no dependency of fRH(%RH,Dry) with size for absorbing substances in contrast to the decreasing exponential behavior with size for purely scattering substances, but no discernable difference could be made between the two wavelengths used. Less than 5% 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

  6. Refractive Index and Absorption Attribution of Highly Absorbing Brown Carbon Aerosols from an Urban Indian City-Kanpur

    NASA Astrophysics Data System (ADS)

    Shamjad, P. M.; Tripathi, S. N.; Thamban, Navaneeth M.; Vreeland, Heidi

    2016-11-01

    Atmospheric aerosols influence Earth’s radiative balance, having both warming and cooling effects. Though many aerosols reflect radiation, carbonaceous aerosols such as black carbon and certain organic carbon species known as brown carbon have the potential to warm the atmosphere by absorbing light. Black carbon absorbs light over the entire solar spectrum whereas brown carbon absorbs near-UV wavelengths and, to a lesser extent, visible light. In developing countries, such as India, where combustion sources are prolific, the influence of brown carbon on absorption may be significant. In order to better characterize brown carbon, we present experimental and modeled absorption properties of submicron aerosols measured in an urban Indian city (Kanpur). Brown carbon here is found to be fivefold more absorbing at 365 nm wavelength compared to previous studies. Results suggest ~30% of total absorption in Kanpur is attributed to brown carbon, with primary organic aerosols contributing more than secondary organics. We report the spectral brown carbon refractive indices along with an experimentally constrained estimate of the influence of aerosol mixing state on absorption. We conclude that brown carbon in Kanpur is highly absorbing in nature and that the mixing state plays an important role in light absorption from volatile species.

  7. Refractive Index and Absorption Attribution of Highly Absorbing Brown Carbon Aerosols from an Urban Indian City-Kanpur.

    PubMed

    Shamjad, P M; Tripathi, S N; Thamban, Navaneeth M; Vreeland, Heidi

    2016-11-24

    Atmospheric aerosols influence Earth's radiative balance, having both warming and cooling effects. Though many aerosols reflect radiation, carbonaceous aerosols such as black carbon and certain organic carbon species known as brown carbon have the potential to warm the atmosphere by absorbing light. Black carbon absorbs light over the entire solar spectrum whereas brown carbon absorbs near-UV wavelengths and, to a lesser extent, visible light. In developing countries, such as India, where combustion sources are prolific, the influence of brown carbon on absorption may be significant. In order to better characterize brown carbon, we present experimental and modeled absorption properties of submicron aerosols measured in an urban Indian city (Kanpur). Brown carbon here is found to be fivefold more absorbing at 365 nm wavelength compared to previous studies. Results suggest ~30% of total absorption in Kanpur is attributed to brown carbon, with primary organic aerosols contributing more than secondary organics. We report the spectral brown carbon refractive indices along with an experimentally constrained estimate of the influence of aerosol mixing state on absorption. We conclude that brown carbon in Kanpur is highly absorbing in nature and that the mixing state plays an important role in light absorption from volatile species.

  8. Refractive Index and Absorption Attribution of Highly Absorbing Brown Carbon Aerosols from an Urban Indian City-Kanpur

    PubMed Central

    Shamjad, P. M.; Tripathi, S. N.; Thamban, Navaneeth M.; Vreeland, Heidi

    2016-01-01

    Atmospheric aerosols influence Earth’s radiative balance, having both warming and cooling effects. Though many aerosols reflect radiation, carbonaceous aerosols such as black carbon and certain organic carbon species known as brown carbon have the potential to warm the atmosphere by absorbing light. Black carbon absorbs light over the entire solar spectrum whereas brown carbon absorbs near-UV wavelengths and, to a lesser extent, visible light. In developing countries, such as India, where combustion sources are prolific, the influence of brown carbon on absorption may be significant. In order to better characterize brown carbon, we present experimental and modeled absorption properties of submicron aerosols measured in an urban Indian city (Kanpur). Brown carbon here is found to be fivefold more absorbing at 365 nm wavelength compared to previous studies. Results suggest ~30% of total absorption in Kanpur is attributed to brown carbon, with primary organic aerosols contributing more than secondary organics. We report the spectral brown carbon refractive indices along with an experimentally constrained estimate of the influence of aerosol mixing state on absorption. We conclude that brown carbon in Kanpur is highly absorbing in nature and that the mixing state plays an important role in light absorption from volatile species. PMID:27883083

  9. Absorbing Aerosols Workshop, January 20-21, 2016

    SciTech Connect

    Nasiri, Shaima; Williamson, Ashley; Cappa, Christopher D.; Kotamarthi, Davis Rao; Sedlacek, Arthur J.; Flynn, Conner; Lewis, Ernie; McComiskey, Allison; Riemer, Nicole

    2016-07-01

    A workshop was held at DOE Headquarters on January 20-21, 2016 during which experts within and outside DOE were brought together to identify knowledge gaps in modeling and measurement of the contribution of absorbing aerosols (AA) to radiative forcing. Absorbing aerosols refer to those aerosols that absorb light, whereby they both reduce the amount of sunlight reaching the surface (direct effect) and heat their surroundings. By doing so, they modify the vertical distribution of heat in the atmosphere and affect atmospheric thermodynamics and stability, possibly hastening cloud drop evaporation, and thereby affecting cloud amount, formation, dissipation and, ultimately, precipitation. Deposition of AA on snow and ice reduces surface albedo leading to accelerated melt. The most abundant AA type is black carbon (BC), which results from combustion of fossil fuel and biofuel. The other key AA types are brown carbon (BrC), which also results from combustion of fossil fuel and biofuel, and dust (crustal material). Each of these sources may result from, and be strongly influenced by, anthropogenic activities. The properties and amounts of AA depend upon various factors, primarily fuel source and burn conditions (e.g., internal combustion engine, flaming or smoldering wildfire), vegetation type (in the case of BC and BrC), and in the case of dust, soil type and ground cover (i.e., vegetation, snow, etc.). After emission, AA undergo chemical processing in the atmosphere that affects their physical and chemical properties. Thus, attribution of sources of AA, and understanding processes AA undergo during their atmospheric lifetimes, are necessary to understand how they will behave in a changing climate.

  10. Interpretation of FRESCO cloud retrievals in case of absorbing aerosol events

    NASA Astrophysics Data System (ADS)

    Wang, P.; Tuinder, O. N. E.; Tilstra, L. G.; de Graaf, M.; Stammes, P.

    2012-10-01

    Cloud and aerosol information is needed in trace gas retrievals from satellite measurements. The Fast REtrieval Scheme for Clouds from the Oxygen A band (FRESCO) cloud algorithm employs reflectance spectra of the O2 A band around 760 nm to derive cloud pressure and effective cloud fraction. In general, clouds contribute more to the O2 A band reflectance than aerosols. Therefore, the FRESCO algorithm does not correct for aerosol effects in the retrievals and attributes the retrieved cloud information entirely to the presence of clouds, and not to aerosols. For events with high aerosol loading, aerosols may have a dominant effect, especially for almost cloud free scenes. We have analysed FRESCO cloud data and Absorbing Aerosol Index (AAI) data from the Global Ozone Monitoring Experiment (GOME-2) instrument on the Metop-A satellite for events with typical absorbing aerosol types, such as volcanic ash, desert dust and smoke. We find that the FRESCO effective cloud fractions are correlated with the AAI data for these absorbing aerosol events and that the FRESCO cloud pressure contains information on aerosol layer pressure. For cloud free scenes, the derived FRESCO cloud pressure is close to the aerosol layer pressure, especially for optically thick aerosol layers. For cloudy scenes, if the strongly absorbing aerosols are located above the clouds, then the retrieved FRESCO cloud pressure may represent the height of the aerosol layer rather than the height of the clouds. Combining FRESCO and AAI data, an estimate for the aerosol layer pressure can be given.

  11. Optical Properties and Aging of Light Absorbing Secondary Organic Aerosol

    SciTech Connect

    Liu, Jiumeng; Lin, Peng; Laskin, Alexander; Laskin, Julia; Kathmann, Shawn M.; Wise, Matthew E.; Caylor, Ryan; Imholt, Felisha; Selimovic, Vanessa; Shilling, John E.

    2016-10-14

    The light-absorbing organic aerosol (OA), commonly referred to as “brown carbon (BrC)”, has attracted considerable attention in recent years because of its potential to affect atmospheric radiation balance, especially in the ultraviolet region and thus impact photochemical processes. A growing amount of data has indicated that BrC is prevalent in the atmosphere, which has motivated numerous laboratory and field studies; however, our understanding of the relationship between the chemical composition and optical properties of BrC remains limited. We conducted chamber experiments to investigate the effect of various VOC precursors, NOx concentrations, photolysis time and relative humidity (RH) on the light absorption of selected secondary organic aerosols (SOA). Light absorption of chamber generated SOA samples, especially aromatic SOA, was found to increase with NOx concentration, at moderate RH, and for the shortest photolysis aging times. The highest mass absorption coefficients (MAC) value is observed from toluene SOA products formed under high NOx conditions at moderate RH, in which nitro-aromatics were previously identified as the major light absorbing compounds. BrC light absorption is observed to decrease with photolysis time, correlated with a decline of the organonitrate fraction of SOA. SOA formed from mixtures of aromatics and isoprene absorb less visible and UV light than SOA formed from aromatic precursors alone on a mass basis. However, the mixed-SOA absorption was underestimated when optical properties were predicted using a two-product SOA formation model, as done in many current climate models. Further investigation, including analysis on detailed mechanisms, are required to explain the discrepancy.

  12. Black carbon and other light-absorbing aerosols in snow

    NASA Astrophysics Data System (ADS)

    Wang, X.; Doherty, S. J.; Warren, S. G.; Fu, Q.

    2011-12-01

    Black carbon (BC), organic carbon (OC), and mineral dust are the most important light-absorbing aerosols (LAA) in snow. The physical, chemical and optical properties of these aerosols differ greatly; the different spectral dependences of their light-absorption can be used to quantify their concentrations in snow. A field campaign was conducted in January and February of 2010 to measure the LAA in snow across northern China. About 400 snow samples were collected at 46 sites in 6 provinces (Huang et al. 2011). Light absorption by mineral dust is due to iron oxides, so iron was determined by chemical analysis of filters and meltwater. To obtain concentrations of the absorbers, BC, OC, and Fe were assumed to have mass absorption cross-sections at 550 nm of 6.3, 0.3, and 0.9 m2/g respectively, and absorption Ångstrom exponents of 1.1, 6, and 3. The lowest values of all LAA are in the remote northeast, at latitude 51°N on the border of Siberia.Median values in surface snow there are 75 ppb BC, 150 ppb OC, and 45 ppb Fe. Farther south, in the industrial northeast, median values are 1000 ppb BC, 4200 ppb OC, and 500 ppb Fe. The grassland of Inner Mongolia is dominated by OC in soil dust of local origin: 560 ppb BC, 8000 ppb OC, 430 ppb Fe. In the Qilian Mountains at the northern boundary of the Tibetan Plateau the surface snow has 70 ppb BC, 2800 ppb OC, and 550 ppb Fe. The fraction of light absorption due to Fe is ~30% in the Qilian Mountains. Elsewhere BC and OC dominate the absorption, so Fe contributes <10% even though the Fe concentrations are as high as the Qilian values.

  13. Extending MODIS Deep Blue Aerosol Retrieval Coverage to Cases of Absorbing Aerosols Above Clouds: First Results

    NASA Technical Reports Server (NTRS)

    Sayer, A. M.; Hsu, N. C.; Bettenhausen, C.; Lee, J.; Redemann, J.; Shinozuka, Y.; Schmid, B.

    2015-01-01

    Absorbing smoke or mineral dust aerosols above clouds (AAC) are a frequent occurrence in certain regions and seasons. Operational aerosol retrievals from sensors like MODIS omit AAC because they are designed to work only over cloud-free scenes. However, AAC can in principle be quantified by these sensors in some situations (e.g. Jethva et al., 2013; Meyer et al., 2013). We present a summary of some analyses of the potential of MODIS-like instruments for this purpose, along with two case studies using airborne observations from the Ames Airborne Tracking Sunphotometer (AATS; http://geo.arc.nasa.gov/sgg/AATS-website/) as a validation data source for a preliminary AAC algorithm applied to MODIS measurements. AAC retrievals will eventually be added to the MODIS Deep Blue (Hsu et al., 2013) processing chain.

  14. Interpretation of FRESCO cloud retrievals in case of absorbing aerosol events

    NASA Astrophysics Data System (ADS)

    Wang, P.; Tuinder, O. N. E.; Tilstra, L. G.; Stammes, P.

    2011-12-01

    Cloud and aerosol information is needed in trace gas retrievals from satellite measurements. The Fast REtrieval Scheme for Clouds from the Oxygen A band (FRESCO) cloud algorithm employs reflectance spectra of the O2 A band around 760 nm to derive cloud pressure and effective cloud fraction. In general, clouds contribute more to the O2 A band reflectance than aerosols. Therefore, the FRESCO algorithm does not correct for aerosol effects in the retrievals and attributes the retrieved cloud information entirely to the presence of clouds, and not to aerosols. For events with high aerosol loading, aerosols may have a dominant effect, especially for almost cloud-free scenes. We have analysed FRESCO cloud data and Absorbing Aerosol Index (AAI) data from the Global Ozone Monitoring Experiment (GOME-2) instrument on the Metop-A satellite for events with typical absorbing aerosol types, such as volcanic ash, desert dust and smoke. We find that the FRESCO effective cloud fractions are correlated with the AAI data for these absorbing aerosol events and that the FRESCO cloud pressures contain information on aerosol layer pressure. For cloud-free scenes, the derived FRESCO cloud pressures are close to those of the aerosol layer for optically thick aerosols. For cloudy scenes, if the strongly absorbing aerosols are located above the clouds, then the retrieved FRESCO cloud pressures may represent the height of the aerosol layer rather than the height of the clouds. Combining FRESCO cloud data and AAI, an estimate for the aerosol layer pressure can be given, which can be beneficial for aviation safety and operations in case of e.g. volcanic ash plumes.

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

    NASA Astrophysics Data System (ADS)

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

    2017-02-01

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

  16. Impacts of Snow Darkening by Absorbing Aerosols on Eurasian Climate

    NASA Technical Reports Server (NTRS)

    Kim, Kyu-Myong; Lau, William K M.; Yasunari, Teppei J.; Kim, Maeng-Ki; Koster, Randal D.

    2016-01-01

    The deposition of absorbing aerosols on snow surfaces reduces snow-albedo and allows snowpack to absorb more sunlight. This so-called snow darkening effect (SDE) accelerates snow melting and leads to surface warming in spring. To examine the impact of SDE on weather and climate during late spring and early summer, two sets of NASA GEOS-5 model simulations with and without SDE are conducted. Results show that SDE-induced surface heating is particularly pronounced in Eurasian regions where significant depositions of dust transported from the North African deserts, and black carbon from biomass burning from Asia and Europe occur. In these regions, the surface heating due to SDE increases surface skin temperature by 3-6 degrees Kelvin near the snowline in spring. Surface energy budget analysis indicates that SDE-induced excess heating is associated with a large increase in surface evaporation, subsequently leading to a significant reduction in soil moisture, and increased risks of drought and heat waves in late spring to early summer. Overall, we find that rainfall deficit combined with SDE-induced dry soil in spring provide favorable condition for summertime heat waves over large regions of Eurasia. Increased frequency of summer heat waves with SDE and the region of maximum increase in heat-wave frequency are found along the snow line, providing evidence that early snowmelt by SDE may increase the risks of extreme summer heat wave. Our results suggest that climate models that do not include SDE may significantly underestimate the effect of global warming over extra-tropical continental regions.

  17. Source apportionment of absorbing aerosols in the central Indo-Gangetic Plain

    NASA Astrophysics Data System (ADS)

    Vaishya, Aditya; Singh, Prayagraj; Rastogi, Shantanu; Babu, S. Suresh

    2016-05-01

    Atmospheric aerosols in the Indo-Gangetic Plain (IGP) depicts high spatial and temporal heterogeneity in their radiative properties. Despite the fact that significant advancement in terms of characterizing aerosols radiative and physiochemical properties in the IGP have been made, information regarding the organic content towards total absorbing aerosol budget is lacking. In the present study we have analyzed two years of aerosol spectral light absorption measurements from the central-IGP, Gorakhpur (26.75°N, 83.38°E, 85m amsl), in order to study their seasonal behavior and to quantify their magnitude in terms of absorbing aerosols loading and source speciation. Remote sensing data in the form of 'Cloud corrected Fire Count' from MODIS Terra and 'Absorption Aerosol Index' from OMI satellites platform have been used to identify absorbing aerosol source regions. Spectral absorption analysis reveals a four-fold enhancement in absorption in the winter (W) and the post-monsoon (PoM) seasons at UV wavelengths as compared to 880 nm on account of increased biomass aerosol contribution to total absorbing aerosol load. Despite having higher fire events and absorption aerosol index, both indicating high biomass burning activities, in the pre-monsoon (PM) season, aerosols from the biomass sources contribute ~ 27% during the W and the PoM seasons as against ~17% in the PM season to the total absorbing aerosol content. This is due to near stagnant wind conditions and shallow height of air masses travelling to the central IGP in the W and the PoM seasons.

  18. Competing Atmospheric and Surface-Driven Impacts of Absorbing Aerosols on the East Asian Summer Monsoon

    NASA Astrophysics Data System (ADS)

    Persad, G.; Paynter, D.; Ming, Y.; Ramaswamy, V.

    2015-12-01

    Absorbing aerosols, by attenuating shortwave radiation within the atmosphere and reemitting it as longwave radiation, redistribute energy both vertically within the surface-atmosphere column and horizontally between polluted and unpolluted regions. East Asia has the largest concentrations of anthropogenic absorbing aerosols globally, and these, along with the region's scattering aerosols, have both reduced the amount of solar radiation reaching the Earth's surface regionally ("solar dimming") and increased shortwave absorption within the atmosphere, particularly during the peak months of the East Asian Summer Monsoon (EASM). We here analyze how atmospheric absorption and surface solar dimming compete in driving the response of EASM circulation to anthropogenic absorbing aerosols, which dominates, and why—issues of particular importance for predicting how the EASM will respond to projected changes in absorbing and scattering aerosol emissions in the future. We probe these questions in a state-of-the-art general circulation model (GCM) using a combination of realistic and idealized aerosol perturbations that allow us to analyze the relative influence of absorbing aerosols' atmospheric and surface-driven impacts on EASM circulation. In combination, our results make clear that, although absorption-driven dimming has a less detrimental effect on EASM circulation than purely scattering-driven dimming, aerosol absorption is still a net impairment to EASM strength when both its atmospheric and surface effects are considered. Because atmospheric heating is not efficiently conveyed to the surface, the surface dimming and associated cooling from even a pure absorber is sufficient to counteract its atmospheric heating, resulting in a net reduction in EASM strength. These findings elevate the current understanding of the impacts of aerosol absorption on the EASM, improving our ability to diagnose EASM responses to current and future regional changes in aerosol emissions.

  19. Identification of absorbing organic (brown carbon) aerosols through Sun Photometry: results from AEROCAN / AERONET stations in high Arctic and urban Locations

    NASA Astrophysics Data System (ADS)

    Kerr, G. H.; Chaubey, J. P.; O'Neill, N. T.; Hayes, P.; Atkinson, D. B.

    2014-12-01

    Light absorbing organic aerosols or brown carbon (BrC) aerosols are prominent species influencing the absorbing aerosol optical depth (AAOD) of the total aerosol optical depth (AOD) in the UV wavelength region. They, along with dust, play an important role in modifying the spectral AAOD and the spectral AOD in the UV region: this property can be used to discriminate BrC aerosols from both weakly absorbing aerosols such as sulfates as well as strongly absorbing aerosols such as black carbon (BC). In this study we use available AERONET inversions (level 1.5) retrieved for the measuring period from 2009 to 2013, for the Arctic region (Eureka, Barrow and Hornsund), Urban/ Industrial regions (Kanpur, Beijing), and the forest regions (Alta Foresta and Mongu), to identify BrC aerosols. Using Dubovik's inversion algorithm results, we analyzed parameters that were sensitive to BrC presence, notably AAOD, AAODBrC estimated using the approach of Arola et al. [2011], the fine-mode-aerosol absorption derivative (αf, abs) and the fine-mode-aerosol absorption 2nd derivative (αf, abs'), all computed at a near UV wavelength (440 nm). Temporal trends of these parameters were investigated for all test stations and compared to available volume sampling surface data as a means of validating / evaluating the sensitivity of ostensible sunphotometer indicators of BrC aerosols to the presence of BrC as measured using independent indicators. Reference: Arola, A., Schuster, G., Myhre, G., Kazadzis, S., Dey, S., and Tripathi, S. N.: Inferring absorbing organic carbon content from AERONET data, Atmos. Chem. Phys., 11, 215-225, doi:10.5194/acp-11-215-2011, 2011

  20. Extending 'Deep Blue' aerosol retrieval coverage to cases of absorbing aerosols above clouds: sensitivity analysis and first case studies

    SciTech Connect

    Sayer, Andrew M.; Hsu, C.; Bettenhausen, Corey; Lee, Jae N.; Redemann, Jens; Schmid, Beat; Shinozuka, Yohei

    2016-05-07

    Cases of absorbing aerosols above clouds (AAC), such as smoke or mineral dust, are omitted from most routinely-processed space-based aerosol optical depth (AOD) data products, including those from the Moderate Resolution Imaging Spectroradiometer (MODIS). This study presents a sensitivity analysis and preliminary algorithm to retrieve above-cloud AOD and liquid cloud optical depth (COD) for AAC cases from MODIS or similar

  1. Global detection of absorbing aerosols over the ocean in the red and near-infrared spectral region

    NASA Astrophysics Data System (ADS)

    Waquet, F.; Péré, J.-C.; Peers, F.; Goloub, P.; Ducos, F.; Thieuleux, F.; Tanré, D.

    2016-09-01

    The spatial and temporal variability of the aerosol single scattering albedo (SSA at 865 nm) has been estimated over clear-sky ocean for 2006 by using measurements acquired by POLDER (Polarization and Directionality of Earth Reflectances). Our estimates are correlated with Sun photometer retrievals (R = 0.63). Differences in SSA are generally around 0.05 and systematically fall below 0.055 for optical thicknesses ≥0.3 (at 865 nm) and modeling errors ≤3.0%. Fine absorbing aerosols (radius ≤ 0.16 μm) are detected in many coastal regions. The lowest SSAs are retrieved over the southeast Atlantic during summer (0.80), whereas nonabsorbing fine particles (≥0.98) are observed over the North Pacific. During winter, fine absorbing aerosols are detected together with mineral dust near the coasts of western Africa (0.90), over the tropical Atlantic (0.88), and around India (0.88). Long-range transport of absorbing species is also detected, as for instance over the Arctic. This study could help to constrain aerosol absorption and radiative forcing in models.

  2. Aerosol therapy in the equine species.

    PubMed

    Duvivier, D H; Votion, D; Vandenput, S; Lekeux, P

    1997-11-01

    Inhalation therapy plays an increasing role in the management of equine respiratory disorders. This alternative to systematic treatment permits a high concentration of medication to act locally while minimizing side effects and residues. In human medicine, literature in this field is prolific and continuously renewed, whereas in veterinary medicine, applications of aerosol therapy are less extensive. This review considers the principles of action of the different types of devices used for inhalation, i.e., nebulization, metered-dose inhalation and dry powder inhalation, describes the technical and practical requirements for their use in the equine species and considers the advantages and disadvantages of each inhalation device. The pharmacological agents currently administered to horses by inhalation are also discussed. Perspectives of aerosol therapy in the equine species, including aerosols already used in human medicine and their potential applications for horses are described.

  3. The effect of absorbing aerosols on Indian monsoon circulation and rainfall: A review

    NASA Astrophysics Data System (ADS)

    Sanap, S. D.; Pandithurai, G.

    2015-10-01

    Aerosol, an uncertain component of the climate system, has attracted wide attention among the researchers due to its role in hydrological cycle and radiation budget in a changing climate. According to IPCC 5th assessment report, current understanding of aerosol-cloud-precipitation interaction is low to moderate, as a result they are not well represented in the climate models, and in turn are recognized as major uncertainties in the future climate projections. In South Asian monsoon regions, the aerosol forcing response to water cycle is even more complicated. Substantial amount of transported dust from Middle East countries and adjacent deserts get accumulated over Indian subcontinent (mainly North India and Indo Gangetic Plains; IGP) and further coated with black carbon (BC) produced from local emission, which make the atmospheric physics and chemistry of the aerosol more complex over the region. Here we review earlier studies and recapitulate our current understanding of absorbing aerosols on Indian monsoon circulation and rainfall from observational evidences and variety of numerical model simulations. This review begins with current understanding of the absorbing aerosols and interactions with Indian summer monsoon, followed by discussion on various working hypotheses, observational and modeling perspective, local and remote impacts. The key open questions and suggestions for future research priorities are delineated to improve the current understanding about the relationship between absorbing aerosols and Indian summer monsoon.

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

    PubMed

    Cheng, Tianhai; Wu, Yu; Chen, Hao

    2014-06-30

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

  5. A multi-satellite analysis of the direct radiative effects of absorbing aerosols above clouds

    NASA Astrophysics Data System (ADS)

    Chang, Y. Y.; Christopher, S. A.

    2015-12-01

    Radiative effects of absorbing aerosols above liquid water clouds in the southeast Atlantic as a function of fire sources are investigated using A-Train data coupled with the Visible Infrared Imaging Radiometer Suite (VIIRS) onboard Suomi National Polar-orbiting Partnership (Suomi NPP). Both the VIIRS Active Fire product and the Aqua Moderate Resolution Imaging Spectroradiometer (MODIS) Thermal Anomalies product (MYD14) are used to identify the biomass burning fire origin in southern Africa. The Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP) are used to assess the aerosol type, aerosol altitude, and cloud altitude. We use back trajectory information, wind data, and the Fire Locating and Modeling of Burning Emissions (FLAMBE) product to infer the transportation of aerosols from the fire source to the CALIOP swath in the southeast Atlantic during austral winter.

  6. Extending "Deep Blue" Aerosol Retrieval Coverage to Cases of Absorbing Aerosols Above Clouds: Sensitivity Analysis and First Case Studies

    NASA Technical Reports Server (NTRS)

    Sayer, A. M.; Hsu, N. C.; Bettenhausen, C.; Lee, J.; Redemann, J.; Schmid, B.; Shinozuka, Y.

    2016-01-01

    Cases of absorbing aerosols above clouds (AACs), such as smoke or mineral dust, are omitted from most routinely processed space-based aerosol optical depth (AOD) data products, including those from the Moderate Resolution Imaging Spectroradiometer (MODIS). This study presents a sensitivity analysis and preliminary algorithm to retrieve above-cloud AOD and liquid cloud optical depth (COD) for AAC cases from MODIS or similar sensors, for incorporation into a future version of the "Deep Blue" AOD data product. Detailed retrieval simulations suggest that these sensors should be able to determine AAC AOD with a typical level of uncertainty approximately 25-50 percent (with lower uncertainties for more strongly absorbing aerosol types) and COD with an uncertainty approximately10-20 percent, if an appropriate aerosol optical model is known beforehand. Errors are larger, particularly if the aerosols are only weakly absorbing, if the aerosol optical properties are not known, and the appropriate model to use must also be retrieved. Actual retrieval errors are also compared to uncertainty envelopes obtained through the optimal estimation (OE) technique; OE-based uncertainties are found to be generally reasonable for COD but larger than actual retrieval errors for AOD, due in part to difficulties in quantifying the degree of spectral correlation of forward model error. The algorithm is also applied to two MODIS scenes (one smoke and one dust) for which near-coincident NASA Ames Airborne Tracking Sun photometer (AATS) data were available to use as a ground truth AOD data source, and found to be in good agreement, demonstrating the validity of the technique with real observations.

  7. Measurement-based estimates of direct radiative effects of absorbing aerosols above clouds

    NASA Astrophysics Data System (ADS)

    Feng, Nan; Christopher, Sundar A.

    2015-07-01

    The elevated layers of absorbing smoke aerosols from western African (e.g., Gabon and Congo) biomass burning activities have been frequently observed above low-level stratocumulus clouds off the African coast, which presents an excellent natural laboratory for studying the effects of aerosols above clouds (AAC) on regional energy balance in tropical and subtropical environments. Using spatially and temporally collocated Moderate Resolution Imaging Spectroradiometer, Ozone Monitoring Instrument (OMI), and Clouds and the Earth's Radiant Energy System data sets, the top-of-atmosphere shortwave aerosol direct shortwave radiative effects (ARE) of absorbing aerosols above low-level water clouds in the southeast Atlantic Ocean was examined in this study. The regional averaged instantaneous ARE has been estimated to be 36.7 ± 20.5 Wm-2 (regional mean ± standard deviation) along with a mean positive OMI Aerosol Index at 1.3 in August 2006 based on multisensors measurements. The highest magnitude of instantaneous ARE can even reach 138.2 Wm-2. We assess that the 660 nm cloud optical depth (COD) values of 8-12 is the critical value above (below) which aerosol absorption (scattering) effect dominates and further produces positive (negative) ARE values. The results further show that ARE values are more sensitive to aerosols above lower COD values than cases for higher COD values. This is among the first studies to provide quantitative estimates of shortwave ARE due to AAC events from an observational perspective.

  8. Absorbing Aerosols: Field and Laboratory Studies of Black Carbon and Dust

    NASA Astrophysics Data System (ADS)

    Aiken, A. C.; Flowers, B. A.; Dubey, M. K.

    2011-12-01

    Currently, absorbing aerosols are thought to be the most uncertain factor in atmospheric climate models (~0.4-1.2 W/m2), and the 2nd most important factor after CO2 in global warming (1.6 W/m2; Ramanathan and Carmichael, Nature Geoscience, 2008; Myhre, Science, 2009). While most well-recognized atmospheric aerosols, e.g., sulfate from power-plants, have a cooling effect on the atmosphere by scattering solar radiation, black carbon (BC or soot) absorbs sunlight strongly which results in a warming of the atmosphere. Dust particles are also present globally and can absorb radiation, contributing to a warmer and drier atmosphere. Direct on-line measurements of BC and hematite, an absorbing dust aerosol, can be made with the Single Particle Soot Photometer (SP2), which measures the mass of the particles by incandescence on an individual particle basis. Measurements from the SP2 are combined with absorption measurements from the three-wavelength photoacoustic soot spectrometer (PASS-3) at 405, 532, and 781 nm and the ultraviolet photoacoustic soot spectrometer (PASS-UV) at 375 nm to determine wavelength-dependent mass absorption coefficients (MACs). Laboratory aerosol samples include flame-generated soot, fullerene soot, Aquadag, hematite, and hematite-containing dusts. Measured BC MAC's compare well with published values, and hematite MAC's are an order of magnitude less than BC. Absorbing aerosols measured in the laboratory are compared with those from ambient aerosols measured during the Las Conchas fire and BEACHON-RoMBAS. The Las Conchas fire was a wildfire in the Jemez Mountains of New Mexico that burned over 100,000 acres during the Summer of 2011, and BEACHON-RoMBAS (Bio-hydro-atmosphere interactions of Energy, Aerosols, Carbon, H2O, Organics & Nitrogen - Rocky Mountain Biogenic Aerosol Study) is a field campaign focusing on biogenic aerosols at the Manitou Forest Observatory near Colorado Springs, CO in Summer 2011. Optical properties and size

  9. The role of anthropogenic species in Biogenic aerosol formation

    EPA Science Inventory

    Isoprene is a widely recognized source of organic aerosol in the southeastern United States. Models have traditionally represented isoprene-derived aerosol as semivolatile species formed from the initial isoprene + OH reaction. Recent laboratory and field studies indicate later g...

  10. Amplification of ENSO effects on Indian summer monsoon by absorbing aerosols

    NASA Astrophysics Data System (ADS)

    Kim, Maeng-Ki; Lau, William K. M.; Kim, Kyu-Myong; Sang, Jeong; Kim, Yeon-Hee; Lee, Woo-Seop

    2016-04-01

    In this study, we present observational evidence, based on satellite aerosol measurements and MERRA reanalysis data for the period 1979-2011, indicating that absorbing aerosols can have strong influence on seasonal-to-interannual variability of the Indian summer monsoon rainfall, including amplification of ENSO effects. We find a significant correlation between ENSO (El Nino Southern Oscillation) and aerosol loading in April-May, with La Nina (El Nino) conditions favoring increased (decreased) aerosol accumulation over northern India, with maximum aerosol optical depth over the Arabian Sea and Northwestern India, indicative of strong concentration of dust aerosols transported from West Asia and Middle East deserts. Composite analyses based on a normalized aerosol index (NAI) show that high concentration of aerosol over northern India in April-May is associated with increased moisture transport, enhanced dynamically induced warming of the upper troposphere over the Tibetan Plateau, and enhanced rainfall over northern India and the Himalayan foothills during May-June, followed by a subsequent suppressed monsoon rainfall over all India, consistent with the elevated heat pump (EHP) hypothesis (Lau et al. in Clim Dyn 26:855-864, 2006. doi: 10.1007/s00382-006-0114-z). Further analyses from sub-sampling of ENSO years, with normal (<1-σ), and abnormal (>1-σ) NAI over northern India respectively show that the EHP may lead to an amplification of the Indian summer monsoon response to ENSO forcing, particularly with respect to the increased rainfall over the Himalayan foothills, and the warming of the upper troposphere over the Tibetan Plateau. Our results suggest that absorbing aerosol, particular desert dusts can strongly modulate ENSO influence, and possibly play important roles as a feedback agent in climate change in Asian monsoon regions.

  11. Absorbing aerosols at high relative humidity: linking hygroscopic growth to optical properties

    NASA Astrophysics Data System (ADS)

    Flores, J. Michel; Bar-Or, R. Z.; Bluvshtein, N.; Abo-Riziq, A.; Kostinski, A.; Borrmann, S.; Koren, I.; Koren, I.; Rudich, Y.

    2012-06-01

    One of the major uncertainties in the understanding of Earth's climate system is the interaction between solar radiation and aerosols in the atmosphere. Aerosols exposed to high humidity will change their chemical, physical, and optical properties due to their increased water content. To model hydrated aerosols, atmospheric chemistry and climate models often use the volume weighted mixing rule to predict the complex refractive index (RI) of aerosols when they interact with high relative humidity, and, in general, assume homogeneous mixing. This study explores the validity of these assumptions. A humidified cavity ring down aerosol spectrometer (CRD-AS) and a tandem hygroscopic DMA (differential mobility analyzer) are used to measure the extinction coefficient and hygroscopic growth factors of humidified aerosols, respectively. The measurements are performed at 80% and 90%RH at wavelengths of 532 nm and 355 nm using size-selected aerosols with different degrees of absorption; from purely scattering to highly absorbing particles. The ratio of the humidified to the dry extinction coefficients (fRHext(%RH, Dry)) is measured and compared to theoretical calculations based on Mie theory. Using the measured hygroscopic growth factors and assuming homogeneous mixing, the expected RIs using the volume weighted mixing rule are compared to the RIs derived from the extinction measurements. We found a weak linear dependence or no dependence of fRH(%RH, Dry) with size for hydrated absorbing aerosols in contrast to the non-monotonically decreasing behavior with size for purely scattering aerosols. No discernible difference could be made between the two wavelengths used. Less than 7% differences were found between the real parts of the complex refractive indices derived and those calculated using the volume weighted mixing rule, and the imaginary parts had up to a 20% difference. However, for substances with growth factor less than 1.15 the volume weighted mixing rule assumption

  12. Radiative effects of absorbing aerosols over northeastern India: Observations and model simulations

    NASA Astrophysics Data System (ADS)

    Gogoi, Mukunda M.; Babu, S. Suresh; Moorthy, K. Krishna; Bhuyan, Pradip Kumar; Pathak, Binita; Subba, Tamanna; Chutia, Lakhima; Kundu, Shyam Sundar; Bharali, Chandrakala; Borgohain, Arup; Guha, Anirban; De, Barin Kumar; Singh, Brajamani; Chin, Mian

    2017-01-01

    Multiyear measurements of spectral properties of aerosol absorption are examined over four geographically distinct locations of northeastern India. Results indicated significant spatiotemporal variation in aerosol absorption coefficients (σabs) with highest values in winter and lowest in monsoon. The western parts of the region, close to the outflow of Indo-Gangetic Plains, showed higher values of σabs and black carbon (BC) concentration—mostly associated with fossil fuel combustion. But, the eastern parts showed higher contributions from biomass-burning aerosols, as much as 20-25% to the total aerosol absorption, conspicuously during premonsoon season. This is attributed to a large number of burning activities over the Southeast Asian region, as depicted from Moderate Resolution Imaging Spectroradiometer fire count maps, whose spatial extent and magnitude peaks during March/April. The nearly consistent high values of aerosol index (AI) and layer height from Ozone Monitoring Instrument indicate the presence of absorbing aerosols in the upper atmosphere. The observed seasonality has been captured fairly well by Goddard Chemistry Aerosol Radiation and Transport (GOCART) as well as Weather Research and Forecasting-Chemistry (WRF-Chem) model simulations. The ratio of column-integrated optical depths due to particulate organic matter and BC from GOCART showed good coincidence with satellite-based observations, indicating the increased vertical dispersion of absorbing aerosols, probably by the additional local convection due to higher fire radiative power caused by the intense biomass-burning activities. In the WRF-Chem though underperformed by different magnitude in winter, the values are closer or overestimated near the burnt areas. Atmospheric forcing due to BC was highest ( 30 Wm-2) over the western part associated with the fossil fuel combustion.

  13. The climate impacts of absorbing aerosols on and within the Arctic

    NASA Astrophysics Data System (ADS)

    Rasch, P.; Wang, H.; Ma, P.; Fast, J. D.; Wang, M.; Easter, R. C.; Liu, X.; Qian, Y.; Flanner, M. G.; Ghan, S.; Singh, B.

    2011-12-01

    Absorbing aerosols are receiving increasing attention as forcing agents in the climate system. By scattering and absorbing light they can reduce planetary albedo, particularly over bright surfaces (clouds, snow and ice). They also act as cloud condensation and/or ice nuclei, influencing the brightness, lifetime and precipitation properties of clouds. Atmospheric stability and primary circulation features respond to the changing vertical and horizontal patterns of heating, cooling, and surface fluxes produced by the aerosols, clouds and surface properties. These changes in meteorology have further impacts on aerosols and clouds producing a complex interplay between transport, forcings, and feedbacks involving absorbing aerosols and climate. The complexity of the processes and the interactions between them make it very challenging to represent aerosols realistically in large scale (global and regional) climate models. Simulations of important features of aerosols still contain easily identifiable biases. I will describe our efforts to identify the processes responsible for some of those biases and the deficiencies in model formulations that impede progress in treating aerosols and understanding their role in polar climate. I plan to summarize some studies performed with the NCAR CESM (global) and WRF-Chem (regional) Community models that examine the simulation sensitivity to treatments of physics, chemistry, and meteorology. Some of these simulations were allowed to evolve freely; others were strongly constrained to agree with observed meteorological fields. We have also altered the formulation of a number of the processes in the model to improve fidelity in the aerosol distributions. The parameterizations used in our global model have also been transferred to the regional model, allowing comparisons to be made between the simpler formulations used in the global model with more elaborate and costly formulations available in the regional model. The regional model can

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

    NASA Technical Reports Server (NTRS)

    Tsay, Si-Chee

    2010-01-01

    Through interaction with clouds and alteration of the Earth's radiation budget, atmospheric aerosols significantly influence our weather and climate. Monsoon rainfalls, for example, sustain the livelihood of more than half of the world's population. Thus, understanding the mechanism that drives the water cycle and freshwater distribution is high-lighted as one of the major near-term goals in NASA's Earth Science Enterprise Strategy. Every cloud droplet/ice-crystal that serves as an essential element in portraying water cycle and distributing freshwater contains atmospheric aerosols at its core. In addition, the spatial and temporal variability of atmospheric aerosol properties is complex due to their dynamic nature. In fact, the predictability of the tropical climate system is much reduced during the boreal spring, which is associated with the peak season of biomass burning activities and regional/long-range transport of dust aerosols. Therefore, to accurately assess the impact of absorbing aerosols on regional-to-global climate requires not only modeling efforts but also continuous observations from satellites, aircraft, networks of ground-based instruments and dedicated field experiments. Since 1997 NASA has been successfully launching a series of satellites the Earth Observing System - to intensively study, and gain a better understanding of, the Earth as an integrated system. Through participation in many satellite remote-sensing/retrieval and validation projects over the years, we have gradually developed and refined the SMART (Surface-sensing Measurements for Atmospheric Radiative Transfer) and COMMIT (Chemical, Optical & Microphysical Measurements of In-situ Troposphere) mobile observatories, a suite of surface remote sensing and in-situ instruments that proved to be vital in providing high temporal measurements, which complement the satellite observations. In this talk, we will present SMART-COMMIT which has played key roles, serving as network or supersite

  15. Effects of Absorbing Aerosols on Accelerated Melting of Snowpack in the Tibetan-Himalayas Region

    NASA Technical Reports Server (NTRS)

    Lau, William K. M.

    2011-01-01

    The impacts of absorbing aerosol on melting of snowpack in the Hindu-Kush-Tibetan-Himalayas (HKTH) region are studied using NASA satellite and GEOS-5 GCM. Results from GCM experiments shows that a 8-10% in the rate of melting of snowpack over the western Himalayas and Tibetan Plateau can be attributed to the aerosol elevated-heat-pump (EHP) feedback effect (Lau et al. 2008), initiated by the absorption of solar radiation by absorbing aerosols accumulated over the Indo-Gangetic Plain and Himalayas foothills. On the other hand, deposition of black carbon on snow surface was estimated to give rise to a reduction in snow surface albedo of 2 - 5%, and an increased annual runoff of 9-24%. From case studies using satellite observations and re-analysis data, we find consistent signals of possible impacts of dust and black carbon aerosol in blackening snow surface, in accelerating spring melting of snowpack in the HKHT, and consequentially in influencing shifts in long-term Asian summer monsoon rainfall pattern.

  16. Light-absorbing Aerosol Properties in the Kathmandu Valley during SusKat-ABC Field Campaign

    NASA Astrophysics Data System (ADS)

    Kim, S.; Yoon, S.; Kim, J.; Cho, C.; Jung, J.

    2013-12-01

    Light-absorbing aerosols, such as black carbon (BC), are major contributors to the atmospheric heating and the reduction of solar radiation reaching at the earth's surface. In this study, we investigate light-absorption and scattering properties of aerosols (i.e., BC mass concentration, aerosol solar-absorption/scattering efficiency) in the Kathmandu valley during Sustainable atmosphere for the Kathmandu valley (SusKat)-ABC campaign, from December 2012 to February 2013. Kathmandu City is among the most polluted cities in the world. However, there are only few past studies that provide basic understanding of air pollution in the Kathmandu Valley, which is not sufficient for designing effective mitigation measures (e.g., technological, financial, regulatory, legal and political measures, planning strategies). A distinct diurnal variation of BC mass concentration with two high peaks observed during wintertime dry monsoon period. BC mass concentration was found to be maximum around 09:00 and 20:00 local standard time (LST). Increased cars and cooking activities including substantial burning of wood and other biomass in the morning and in the evening contributed to high BC concentration. Low BC concentrations during the daytime can be explain by reduced vehicular movement and cooking activities. Also, the developmements of the boundary layer height and mountain-valley winds in the Kathmandu Valley paly a crucial role in the temproal variation of BC mass concentrations. Detailed radiative effects of light-absorbing aerosols will be presented.

  17. Estimation of columnar concentrations of absorbing and scattering fine mode aerosol components using AERONET data

    NASA Astrophysics Data System (ADS)

    Choi, Yongjoo; Ghim, Young Sung

    2016-11-01

    Columnar concentrations of absorbing and scattering components of fine mode aerosols were estimated using Aerosol Robotic Network (AERONET) data for a site downwind of Seoul. The study period was between March 2012 and April 2013 including the period of the Distributed Regional Aerosol Gridded Observation Networks (DRAGON)-Asia campaign in March to May 2012. The Maxwell Garnett mixing rule was assumed for insoluble components embedded in a host solution, while the volume average mixing rule was assumed for the aqueous solution of soluble components. During the DRAGON-Asia campaign the surface concentrations of major components of fine particles were measured. The columnar mass fractions of black carbon (BC), organic carbon (OC), mineral dust (MD), and ammonium sulfate (AS) were 1.5, 5.9, 6.6, and 52%, respectively, which were comparable to the mass fractions measured at the surface for BC, OC, and secondary inorganic aerosols at 2.3, 18, and 55%. The vertical distributions of BC and AS were investigated by employing the concept of a column height. While the column height for BC was similar to the planetary boundary layer (PBL) height, that for AS was 4.4 times higher than the PBL height and increased with air temperature from March to May. The monthly variations of the columnar mass concentrations during the study period were generally well explained in term of meteorology and emission characteristics. However, certain variations of MD were different from those typically observed primarily because only fine mode aerosols were considered.

  18. Vegetation fires, absorbing aerosols and smoke plume characteristics in diverse biomass burning regions of Asia

    NASA Astrophysics Data System (ADS)

    Prasad Vadrevu, Krishna; Lasko, Kristofer; Giglio, Louis; Justice, Chris

    2015-10-01

    In this study, we explored the relationships between the satellite-retrieved fire counts (FC), fire radiative power (FRP) and aerosol indices using multi-satellite datasets at a daily time-step covering ten different biomass burning regions in Asia. We first assessed the variations in MODIS-retrieved aerosol optical depths (AOD’s) in agriculture, forests, plantation and peat land burning regions and then used MODIS FC and FRP (hereafter FC/FRP) to explain the variations in AOD characteristics. Results suggest that tropical broadleaf forests in Laos burn more intensively than the other vegetation fires. FC/FRP-AOD correlations in different agricultural residue burning regions did not exceed 20% whereas in forest regions they reached 40%. To specifically account for absorbing aerosols, we used Ozone Monitoring Instrument-derived aerosol absorption optical depth (AAOD) and UV aerosol index (UVAI). Results suggest relatively high AAOD and UVAI values in forest fires compared with peat and agriculture fires. Further, FC/FRP could explain a maximum of 29% and 53% of AAOD variations, whereas FC/FRP could explain at most 33% and 51% of the variation in agricultural and forest biomass burning regions, respectively. Relatively, UVAI was found to be a better indicator than AOD and AAOD in both agriculture and forest biomass burning plumes. Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observations data showed vertically elevated aerosol profiles greater than 3.2-5.3 km altitude in the forest fire plumes compared to 2.2-3.9 km and less than 1 km in agriculture and peat-land fires, respectively. We infer the need to assimilate smoke plume height information for effective characterization of pollutants from different sources.

  19. A ten-year global record of absorbing aerosols above clouds from OMI's near-UV observations

    NASA Astrophysics Data System (ADS)

    Jethva, Hiren; Torrres, Omar; Ahn, Changwoo

    2016-05-01

    Aerosol-cloud interaction continues to be one of the leading uncertain components of climate models, primarily due to the lack of an adequate knowledge of the complex microphysical and radiative processes associated with the aerosolcloud system. The situations when aerosols and clouds are found in the same atmospheric column, for instance, when light-absorbing aerosols such as biomass burning generated carbonaceous particles or wind-blown dust overlay low-level cloud decks, are commonly found over several regional of the world. Contrary to the cloud-free scenario over dark surface, for which aerosols are known to produce a net cooling effect (negative radiative forcing) on climate, the overlapping situation of absorbing aerosols over cloud can potentially exert a significant level of atmospheric absorption and produces a positive radiative forcing at top-of-atmosphere. The magnitude of direct radiative effects of aerosols above cloud depends directly on the aerosol loading, microphysical-optical properties of the aerosol layer and the underlying cloud deck, and geometric cloud fraction. We help in addressing this problem by introducing a novel product of optical depth of absorbing aerosols above clouds retrieved from near-UV observations made by the Ozone Monitoring Instrument (OMI) on board NASA's Aura platform. The presence of absorbing aerosols above cloud reduces the upwelling radiation reflected by cloud and produces a strong `color ratio' effect in the near-UV region, which can be unambiguously detected in the OMI measurements. Physically based on this effect, the OMACA algorithm retrieves the optical depths of aerosols and clouds simultaneously under a prescribed state of atmosphere. The algorithm architecture and results from a ten-year global record including global climatology of frequency of occurrence and above-cloud aerosol optical depth, and a discussion on related future field campaigns are presented.

  20. Source Attribution of Light-absorbing Aerosols in Arctic Snow (Invited)

    NASA Astrophysics Data System (ADS)

    Hegg, D.; Warren, S. G.; Grenfell, T. C.; Doherty, S. J.; Larson, T. V.; Clarke, A. D.

    2010-12-01

    Light-absorbing aerosols (LAA) deposited on the arctic snow pack, in particular black carbon (BC), contribute appreciably to the arctic radiation budget and their reduction has been suggested as a means to attenuate warming in the arctic. Effective prediction and mitigation of Arctic snow LAA requires that the sources of the LAA be elucidated. To this end, receptor modeling in the form of Positive Matrix Factorization (PMF) has been exercised on a data set of chemical concentrations in snow of various species (including inorganic and organic acids, carbohydrates and selected other organics as well as LAA) derived from an extensive set of snow samples from locations in Russia (including Siberia), Canada, Greenland, the Arctic Ocean and Svalbard. The data were obtained in three distinct periods: spring of 2007, spring of 2008, and spring of 2009. Data from each period were analyzed separately (note that the Svalbard data were analyzed only recently and were not included in the published 2007 analysis). Aerosol light absorption was determined spectrophotometrically at multiple wavelengths on filters through which melted snow was filtered. Based on the Angstrom exponent of the light absorption, partitioning of the absorption between BC and other LAA species was estimated. Statistics of the LAA concentrations for the Arctic as a whole and the geographic distribution of BC and other LAA species are presented. PMF analysis of the filtrate and filters from the 2007 data set from western Siberia, the Canadian lower arctic and Greenland revealed four factors or sources: two distinct biomass burning sources, a pollution source and a marine source. The first three of these were responsible for essentially all of the black carbon, with the two biomass sources together accounting for > 90% of the black carbon. Geographically, the biomass sources were dominant for all regions except the Arctic Ocean near the North Pole. For the 2008 and 2009 data sets, from eastern Siberia and

  1. Modeling investigation of light-absorbing aerosols in the Amazon Basin during the wet season

    NASA Astrophysics Data System (ADS)

    Wang, Qiaoqiao; Saturno, Jorge; Chi, Xuguang; Walter, David; Lavric, Jost V.; Moran-Zuloaga, Daniel; Ditas, Florian; Pöhlker, Christopher; Brito, Joel; Carbone, Samara; Artaxo, Paulo; Andreae, Meinrat O.

    2016-11-01

    We use a global chemical transport model (GEOS-Chem) to interpret observed light-absorbing aerosols in Amazonia during the wet season. Observed aerosol properties, including black carbon (BC) concentration and light absorption, at the Amazon Tall Tower Observatory (ATTO) site in the central Amazon have relatively low background levels but frequently show high peaks during the study period of January-April 2014. With daily temporal resolution for open fire emissions and modified aerosol optical properties, our model successfully captures the observed variation in fine/coarse aerosol and BC concentrations as well as aerosol light absorption and its wavelength dependence over the Amazon Basin. The source attribution in the model indicates the important influence of open fire on the observed variances of aerosol concentrations and absorption, mainly from regional sources (northern South America) and from northern Africa. The contribution of open fires from these two regions is comparable, with the latter becoming more important in the late wet season. The analysis of correlation and enhancement ratios of BC versus CO suggests transport times of < 3 days for regional fires and ˜ 11 days for African plumes arriving at ATTO during the wet season. The model performance of long-range transport of African plumes is also evaluated with observations from AERONET, MODIS, and CALIOP. Simulated absorption aerosol optical depth (AAOD) averaged over the wet season is lower than 0.0015 over the central Amazon, including the ATTO site. We find that more than 50 % of total absorption at 550 nm is from BC, except for the northeastern Amazon and the Guianas, where the influence of dust becomes significant (up to 35 %). The brown carbon contribution is generally between 20 and 30 %. The distribution of absorption Ångström exponents (AAE) suggests more influence from fossil fuel combustion in the southern part of the basin (AAE ˜ 1) but more open fire and dust influence in the

  2. Role of Black Carbon and Absorbing Organic Carbon Aerosols in Surface Dimming Trends

    NASA Astrophysics Data System (ADS)

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

    2010-12-01

    Solar radiation reaching at the Earth’s surface plays an essential role in driving both atmosphere hydrological and land/ocean biogeochemical processes. Measurements have shown significant decreases in surface solar radiation (dimming) in many regions since 1960s. At least half of the observed dimming could be linked to the direct radiative effect of anthropogenic aerosols, especially absorbing aerosols like black carbon (BC) due to their strong atmospheric absorption. However, previous model-data comparisons indicate that absorption by aerosols is commonly and significantly underestimated in current GCM simulations by several factors over regions. Using a global chemical transport model coupled with a radiative transfer model, we include a treatment for absorbing organic carbons (OC) from bio-fuel and open biomass burnings in optical calculations and estimate aerosol radiative forcings for two anthropogenic aerosol emission scenarios representative of 1975 and 2000. Assumptions about aerosol mixing and the OC absorption spectrum are examined by comparing simulated atmospheric heating against aircraft optical and radiation measurements. The calculated aerosol single scattering albedo distribution (0.93+/-0.044) is generally comparable to the AERONET data (0.93+/-0.030) for year 2001, with best agreements in Europe and N. America, while overestimated in E. Asia and underestimated in the S. American biomass burning areas. On a global scale, inclusion of absorbing OC enhances the absorption in the atmosphere by 11% for July. The estimated aerosol direct radiative forcing at TOA (-0.24 W/m2) is similar to the average value of the AeroCom models based on the same 2000 emissions, but significantly enhanced negatively at surface by about 53% (-1.56 W/m2) and the atmosphere absorption is increased by +61% (+1.32 W/m2). About 87% of the estimated atmosphere absorption and 42% of the surface dimming is contributed by BC. Between 1975 and 2000, the calculated all-sky flux

  3. Absorbing aerosols at high relative humidity: closure between hygroscopic growth and optical properties

    NASA Astrophysics Data System (ADS)

    Flores, J. M.; Bar-Or, R. Z.; Bluvshtein, N.; Abo-Riziq, A.; Kostinski, A.; Borrmann, S.; Koren, I.; Rudich, Y.

    2012-01-01

    The extinction coefficient and growth factor of humidified aerosols, at 80% and 90% RH, and at 532 nm and 355 nm wavelengths were measured for size-selected particles for ammonium sulfate, IHSS Pahokee peat (a lightly absorbing humic-like substance proxy), nigrosine (a black dye to model highly absorbing substances), and a mixture of AS and nigrosine. The ratio of the humidified extinction coefficients to the dry (fRHext(%RH, Dry)) was explored. The measured fRHext(%RH, Dry) was compared to theoretical calculations based on Mie theory, using the measured growth factors and assuming homogeneous mixing. The expected complex refractive indices (RIs) using the volume weighted mixing rule were compared to the RIs derived from the extinction measurements. Moreover, the differences between assuming a core-shell structure or a homogeneous mixing of the substances is examined. The laboratory results were used as a basis to model the change in the total extinction, the single scattering albedo (ω), and the asymmetry parameter (g) in the twilight zone of clouds at 355 nm and 532 nm. We found slightly linear to no dependency of fRH(%RH, Dry) with size for absorbing substances in contrast to the decreasing exponential behavior with size for purely scattering substances. However, no discernable difference could be made between the two wavelengths used. Less than 5% 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. Moreover, for substances with growth factor less than 1.15 there was, in average, less than 5% difference between the extinction efficiencies calculated using a core-shell model and assuming homogeneous mixing for size parameters less than 2.5. For x>2.5 the differences were greater causing and overestimation of the extinction efficiency (Qext) values if homogenous mixing was assume instead of a core-shell structure. The

  4. A study on the temporal and spatial variability of absorbing aerosols using Total Ozone Mapping Spectrometer and Ozone Monitoring Instrument Aerosol Index data

    NASA Astrophysics Data System (ADS)

    Li, Jing; Carlson, Barbara E.; Lacis, Andrew A.

    2009-05-01

    Absorbing aerosols, especially mineral dust and black carbon, play key roles in climate change by absorbing solar radiation, heating the atmosphere, and contributing to global warming. In this paper, we first examine the consistency of the Aerosol Index (AI) product as measured by the Total Ozone Mapping Spectrometer (TOMS) and Ozone Monitoring Instrument (OMI) instruments and then analyze these AI data sets to investigate the temporal and spatial variability of UV absorbing aerosols. In contrast to the trend in aerosol optical depth found in the advanced very high-resolution radiometer data, no obvious long-term trend in absorbing aerosols is observed from the time series of AI records. The comparison between the mean annual cycle in the two data sets shows that the cycles agree very well both globally and regionally, indicating a consistency between the AI products from TOMS and OMI. Varimax rotated Empirical Orthogonal Function (EOF) analysis of detrended, deseasonalized AI data proves to be successful in isolating major dust and biomass burning source regions, as well as dust transport. Finally, we find that large, individual events, such as the Kuwait oil fire and Australian smoke plum, are isolated in individual higher-order principal components.

  5. The interplay between assumed morphology and the direct radiative effect of light-absorbing organic aerosol

    NASA Astrophysics Data System (ADS)

    Saleh, Rawad; Adams, Peter J.; Donahue, Neil M.; Robinson, Allen L.

    2016-08-01

    Mie theory is widely employed in aerosol top-of-the-atmosphere direct radiative effect (DRE) calculations and to retrieve the absorptivity of light-absorbing organic aerosol (OA) from measurements. However, when OA is internally mixed with black carbon, it may exhibit complex morphologies whose optical behavior is imperfectly predicted by Mie theory, introducing bias in the retrieved absorptivities. We performed numerical experiments and global radiative transfer modeling (RTM) to investigate the effect of this bias on the calculated absorption and thus the DRE. We show that using true OA absorptivity, retrieved with a realistic representation of the complex morphology, leads to significant errors in DRE when the RTM employs the simplified Mie theory. On the other hand, when Mie theory is consistently applied in both OA absorptivity retrieval and the RTM, the errors largely cancel out, yielding accurate DRE. As long as global RTMs use Mie theory, they should implement parametrizations of light-absorbing OA derived from retrievals based on Mie theory.

  6. Optical properties and aging of light-absorbing secondary organic aerosol

    DOE PAGES

    Liu, Jiumeng; Lin, Peng; Laskin, Alexander; ...

    2016-10-14

    The light-absorbing organic aerosol (OA) commonly referred to as “brown carbon” (BrC) has attracted considerable attention in recent years because of its potential to affect atmospheric radiation balance, especially in the ultraviolet region and thus impact photochemical processes. A growing amount of data has indicated that BrC is prevalent in the atmosphere, which has motivated numerous laboratory and field studies; however, our understanding of the relationship between the chemical composition and optical properties of BrC remains limited. We conducted chamber experiments to investigate the effect of various volatile organic carbon (VOC) precursors, NOx concentrations, photolysis time, and relative humidity (RH) on the light absorptionmore » of selected secondary organic aerosols (SOA). Light absorption of chamber-generated SOA samples, especially aromatic SOA, was found to increase with NOx concentration, at moderate RH, and for the shortest photolysis aging times. The highest mass absorption coefficient (MAC) value is observed from toluene SOA products formed under high-NOx conditions at moderate RH, in which nitro-aromatics were previously identified as the major light-absorbing compounds. BrC light absorption is observed to decrease with photolysis time, correlated with a decline of the organic nitrate fraction of SOA. SOA formed from mixtures of aromatics and isoprene absorb less visible (Vis) and ultraviolet (UV) light than SOA formed from aromatic precursors alone on a mass basis. However, the mixed SOA absorption was underestimated when optical properties were predicted using a two-product SOA formation model, as done in many current climate models. Further investigation, including analysis on detailed mechanisms, are required to explain the discrepancy.« less

  7. Optical properties and aging of light-absorbing secondary organic aerosol

    NASA Astrophysics Data System (ADS)

    Liu, Jiumeng; Lin, Peng; Laskin, Alexander; Laskin, Julia; Kathmann, Shawn M.; Wise, Matthew; Caylor, Ryan; Imholt, Felisha; Selimovic, Vanessa; Shilling, John E.

    2016-10-01

    The light-absorbing organic aerosol (OA) commonly referred to as "brown carbon" (BrC) has attracted considerable attention in recent years because of its potential to affect atmospheric radiation balance, especially in the ultraviolet region and thus impact photochemical processes. A growing amount of data has indicated that BrC is prevalent in the atmosphere, which has motivated numerous laboratory and field studies; however, our understanding of the relationship between the chemical composition and optical properties of BrC remains limited. We conducted chamber experiments to investigate the effect of various volatile organic carbon (VOC) precursors, NOx concentrations, photolysis time, and relative humidity (RH) on the light absorption of selected secondary organic aerosols (SOA). Light absorption of chamber-generated SOA samples, especially aromatic SOA, was found to increase with NOx concentration, at moderate RH, and for the shortest photolysis aging times. The highest mass absorption coefficient (MAC) value is observed from toluene SOA products formed under high-NOx conditions at moderate RH, in which nitro-aromatics were previously identified as the major light-absorbing compounds. BrC light absorption is observed to decrease with photolysis time, correlated with a decline of the organic nitrate fraction of SOA. SOA formed from mixtures of aromatics and isoprene absorb less visible (Vis) and ultraviolet (UV) light than SOA formed from aromatic precursors alone on a mass basis. However, the mixed SOA absorption was underestimated when optical properties were predicted using a two-product SOA formation model, as done in many current climate models. Further investigation, including analysis on detailed mechanisms, are required to explain the discrepancy.

  8. Aerosol distributions and radiative forcing over the Asian Pacific region simulated by Spectral Radiation-Transport Model for Aerosol Species (SPRINTARS)

    NASA Astrophysics Data System (ADS)

    Takemura, Toshihiko; Nakajima, Teruyuki; Higurashi, Akiko; Ohta, Sachio; Sugimoto, Nobuo

    2003-12-01

    A three-dimensional aerosol transport-radiation model coupled with a general circulation model, Spectral Radiation-Transport Model for Aerosol Species (SPRINTARS), simulates atmospheric aerosol distributions and optical properties. The simulated results are compared with aerosol sampling and optical observations from ground, aircraft, and satellite acquired by intensive observation campaigns over east Asia in spring 2001. Temporal variations of the aerosol concentrations, optical thickness, and Ångström exponent are in good agreement between the simulation and observations. The midrange values of the Ångström exponent, even at the Asian dust storm events over the outflow regions, suggest that the contribution of the anthropogenic aerosol, such as carbonaceous and sulfate, to the total optical thickness is of an order comparable to that of the Asian dust. The radiative forcing by the aerosol direct and indirect effects is also calculated. The negative direct radiative forcing is simulated to be over -10 W m-2 at the tropopause in the air mass during the large-scale dust storm, to which both anthropogenic aerosols and Asian dust contribute almost equivalently. The direct radiative forcing, however, largely depends on the cloud water content and the vertical profiles of aerosol and cloud. The simulation shows that not only sulfate and sea salt aerosols but also black carbon and soil dust aerosols, which absorb solar and thermal radiation, make strong negative radiative forcing by the direct effect at the surface, which may exceed the positive forcing by anthropogenic greenhouse gases over the east Asian region.

  9. Disturbance of light-absorbing aerosols on the albedo in a winter snowpack of Central Tibet.

    PubMed

    Ming, Jing; Wang, Pengling; Zhao, Shuyu; Chen, Pengfei

    2013-08-01

    A field observation on the albedo of the snowpack in Central Tibet was conducted in the Nam Co region in the winter of 2011. Snow properties, including grain size and density, were measured in the field, and surface-layer snow samples (down to 5 cm) were collected. The average concentrations of black carbon and dust were 72 ppbm (close to that in the glaciers of Mt. Nyainqentanglha) and 120 ppmm, respectively. Inverse trends were found to exist between the albedo of the snowpack and light-absorbing aerosols (LAAs) as well as grain size growth. Modeling showed that black carbon, dust, and grain growth in the winter snowpack can reduce the broadband albedo by 11%, 28%, and 61%, respectively.

  10. Impacts of absorbing aerosols on interannual and intraseasonal variability of the South Asian monsoon

    NASA Astrophysics Data System (ADS)

    Lau, W. K. M.; Kim, K. M.; Shi, J. J.; Tao, W. K.

    2015-12-01

    Aerosol-monsoon interactions on the interannual and intraseasonal variability of the South Asian monsoon are investigated from observations and modeling. On interannual time scales, we found from observations, and confirm with coupled ocean-atmosphere climate modeling, that absorbing aerosols (mainly desert dust and BC), can significantly amplifying the ENSO impact on the Indian monsoon, through precipitation and circulation feedback induced by the EHP effect. On intraseasonal time scales, modeling studies with the high-resolution WRF regional climate model demonstrated that EHP combined with the semi-direct and microphysics effects, associated with enhanced desert dust transported from the Middle East deserts across the Arabian Sea to the Indian subcontinent, may alter the moisture transport pathways, suppress the development of monsoon depression over northeastern India, resulting in development of intense convective cells, and extreme heavy rain along the Himalayan foothills in central and northwestern India. The implications of these feedback processes on climate change in the South Asian monsoon region will be discussed.

  11. Light-Absorbing Aerosol during NASA GRIP: Overview of Observations in the Free Troposphere and Associated with Tropical Storm Systems

    NASA Astrophysics Data System (ADS)

    Ziemba, L. D.; Beyersdorf, A. J.; Chen, G.; Corr, C. A.; Craig, L.; Dhaniyala, S.; Dibb, J. E.; Hudgins, C. H.; Ismail, S.; Latham, T.; Nenes, A.; Thornhill, K. L.; Winstead, E.; Anderson, B. E.

    2010-12-01

    Aerosols play a significant role in regulating Earth’s climate. Absorbing aerosols typically constitute a small fraction of ambient particle mass but can contribute significantly to direct and indirect climate forcing depending on size, mixing state, concentration, chemical composition, and vertical and spatial distribution. Aerosols may also significantly affect tropical storm/hurricane dynamics through direct light absorption and activation as cloud nuclei. An extensive suite of instrumentation measuring aerosol chemical, physical, and optical properties was deployed aboard the NASA DC-8 to characterize aerosol during the NASA GRIP (Genesis and Rapid Intensification Processes; August-September 2010) mission. The majority of flight time was spent at high altitude (greater than 9 km) and thus much of the sampling was done in the free troposphere, including extensive sampling in the vicinity of tropical storm systems and more diffuse cirrus clouds. With operations based in Fort Lauderdale, FL and St. Croix, U.S. Virgin Islands, a large geographic region was sampled including much of the Gulf of Mexico and tropical Atlantic Ocean. Observations are reported for light-absorbing carbon aerosol (mainly black carbon, BC) primarily using a single particle soot photometer (SP2). The SP2 employs single-particle laser-induced incandescence to provide a mass-specific measurement not subject to scattering interference that is optimal for the low concentration environments like those encountered during GRIP. BC mass concentrations, 100-500 nm size distributions, and mixing state (i.e. coating thickness of scattering material) are presented. Total and sub-micron aerosol absorption coefficients (principally from BC and dust aerosol) are reported using a particle soot absorption photometer (PSAP) along with comparisons with calculated absorption coefficients derived from SP2 observations in various conditions. In addition, dust aerosol is specifically identified using optical and

  12. Amplification of the snow melting effect on the heat wave over the Eurasia by absorbing aerosols

    NASA Astrophysics Data System (ADS)

    Kim, M. K.; Kim, K. M.; Lau, W. K. M.; Sang, J.; Yasunari, T. J.

    2015-12-01

    In this study, we present the potential impact of snow darkening effect on the Eurasian heat wave by absorbing aerosols using the NASA GEOS-5 Model experiments with aerosol tracers and a state-of-the-art snow darkening module for the land surface. Results show that snow darkening effect (SDE) can have a significant influence on not only the intensity but also the duration of heatwave during snow melting season, i.e., late spring season over the mid-western Eurasia and early summer season over the central northern Eurasia. During the early snow melting season surface air temperature is significantly increased by 3-6K due to early snow melting and enhanced solar radiation. Moreover enhanced evaporation induced by surface energy surplus during the early melting season leads to the new equilibrium level with lower soil moisture over the Eurasia since snow melting season, and thereby provide favorable condition for severe droughts and heat wave over the large parts of the Eurasia. This finding suggests that the SDE may play an important role in amplifying the snow melting effect on large-scale heat wave over the Eurasia. Energy and water balance at the surface supporting this findings are also discussed from evaporation-precipitation recycling point of view.

  13. Changes in snow cover and water cycle over the Tibetan plateau induced by absorbing aerosols

    NASA Astrophysics Data System (ADS)

    Lau, W. K.; Kim, M.; Kim, K.; Lee, W.

    2009-12-01

    The warming of the land surface and retreating glacier and snowpack in Hindu-Kush-Himalayas-Tibet (HKHT) are well known observations often attributed to effect of greenhouse warming. In this study, based on numerical experiments with the NASA fvGCM, we find that the elevated -heat-pump (EHP) effect by absorbing aerosols (dust and black carbon) over the Indo-Gangetic Plain and Himalayas foothills can lead to substantial warming of the atmosphere and land surface, and reduction in snow cover over the HKHT region . Atmosphere and surface energy analyses show that beginning in April, the middle atmosphere, near the high-altitude surface over the Tibetan Plateau, heats up due to absorption of solar radiation by black carbon and dust. The near surface heating increases convection, which spreads the warming to the upper troposphere over the Plateau. As the monsoon season approaches in May, the increased convection draws in warmer and moister monsoon air into the HKHT, which further enhances the convection, cloudiness and precipitation over the region in late May and early June. The moister and warmer atmosphere over the HKHT region suppresses evaporation and sensible heat fluxes from the surface during April-May. The excess heat received by the surface goes into melting of the snowpack, exposing more of the bare land. The exposed land surface leads to further increase in land surface temperature over the HKHT. Results show that most of the snow melt occurs in the western region (west of 90E) in April and May, when black carbon aerosol loading in the atmosphere is highest, and dust loading is on the rise. The equivalent surface albedo change due to snow melt is reduced by about 8-10%, and 4-6% over the western and eastern TP respectively. The proposed mechanism appear to be relevant on interannnual time scales and beyond. The consequence of these changes in HKHT on the water cycle of Asia will be discussed.

  14. Assessment of capabilities of multiangle imaging photo-polarimetry for atmospheric correction in presence of absorbing aerosols

    NASA Astrophysics Data System (ADS)

    Kalashnikova, O. V.; Garay, M. J.; Xu, F.; Seidel, F. C.; Diner, D. J.

    2015-12-01

    Satellite remote sensing of ocean color is a critical tool for assessing the productivity of marine ecosystems and monitoring changes resulting from climatic or environmental influences. Yet water-leaving radiance comprises less than 10% of the signal measured from space, making correction for absorption and scattering by the intervening atmosphere imperative. Traditional ocean color retrieval algorithms utilize a standard set of aerosol models and the assumption of negligible water-leaving radiance in the near-infrared. Modern improvements have been developed to handle absorbing aerosols such as urban particulates in coastal areas and transported desert dust over the open ocean, where ocean fertilization can impact biological productivity at the base of the marine food chain. Even so, imperfect knowledge of the absorbing aerosol optical properties or their height distribution results in well-documented sources of error. In the UV, the problem of UV-enhanced absorption and nonsphericity of certain aerosol types are amplified due to the increased Rayleigh and aerosol optical depth, especially at off-nadir view angles. Multi-angle spectro-polarimetric measurements have been advocated as an additional tool to better understand and retrieve the aerosol properties needed for atmospheric correction for ocean color retrievals. The central concern of the work to be described is the assessment of the effects of absorbing aerosol properties on water leaving radiance measurement uncertainty 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. The phase matrices for the spherical smoke particles were calculated using a standard

  15. Measurement of mass distribution of chemical species in aerosol particles

    NASA Technical Reports Server (NTRS)

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

    1984-01-01

    Aerosols may be generated through the nebulizing of solutions and the evaporation of their solvent, leaving the dry solute particles. Attention is presently given to a method for the direct determination of the masses of chemical species in individual aerosol particles on a continuous, real-time basis, using mass spectrometry. After the aerosol particles are introduced into the ion source of a quadrupole mass spectrometer, the particles impinge on a hot rhenium filament in the mass spectrometer's ion source. The resulting vapor plume is ionized by electron bombardment, and a pulse of ions is generated by each particle. The intensities of different masses in the ion pulses can then be measured by the mass spectrometer.

  16. Simultaneous Retrieval of Effective Refractive Index and Density from Size Distribution and Light Scattering Data: Weakly-Absorbing Aerosol

    SciTech Connect

    Kassianov, Evgueni I.; Barnard, James C.; Pekour, Mikhail S.; Berg, Larry K.; Shilling, John E.; Flynn, Connor J.; Mei, Fan; Jefferson, Anne

    2014-10-01

    We propose here a novel approach for retrieving in parallel the effective density and real refractive index of weakly absorbing aerosol from optical and size distribution measurements. Here we define “weakly absorbing” as aerosol single-scattering albedos that exceed 0.95 at 0.5 um.The required optical measurements are the scattering coefficient and the hemispheric backscatter fraction, obtained in this work from an integrating nephelometer. The required size spectra come from a Scanning Mobility Particle Sizer and an Aerodynamic Particle Sizer. The performance of this approach is first evaluated using a sensitivity study with synthetically generated but measurement-related inputs. The sensitivity study reveals that the proposed approach is robust to random noise; additionally the uncertainties of the retrieval are almost linearly proportional to the measurement errors, and these uncertainties are smaller for the real refractive index than for the effective density. Next, actual measurements are used to evaluate our approach. These measurements include the optical, microphysical, and chemical properties of weakly absorbing aerosol which are representative of a variety of coastal summertime conditions observed during the Two-Column Aerosol Project (TCAP; http://campaign.arm.gov/tcap/). The evaluation includes calculating the root mean square error (RMSE) between the aerosol characteristics retrieved by our approach, and the same quantities calculated using the conventional volume mixing rule for chemical constituents. For dry conditions (defined in this work as relative humidity less than 55%) and sub-micron particles, a very good (RMSE~3%) and reasonable (RMSE~28%) agreement is obtained for the retrieved real refractive index (1.49±0.02) and effective density (1.68±0.21), respectively. Our approach permits discrimination between the retrieved aerosol characteristics of sub-micron and sub-10micron particles. The evaluation results also reveal that the

  17. Photoreactivity of condensed species on Titan's aerosols analogues

    NASA Astrophysics Data System (ADS)

    Fleury, Benjamin; Gudipati, Murthy; Carrasco, Nathalie

    2016-10-01

    Titan's aerosols formation is initiated in the upper atmospheric layers at about 1000 km by the dissociation and the ionization of N2 and CH4 by the VUV solar photons [1]. Then, they aggregate and sediment to the surface. The temperatures of the stratosphere and the troposphere [3] (measured by the HASI instrument onboard the Huygens probe [2]) allow the condensation of many volatile organics on the solid aerosols, forming organic ice coating on the aerosol polymers. We will present an experimental study simulating this process and discuss the photoreactivity of condensed species on Titan's aerosols analogues in the atmosphere and on the surface. We demonstrated experimentally that the organic aerosols, which cover the Titan's surface, drive the photoreactivity of condensed species such as acetylene when they are irradiated with long wavelength photons (λ > 300 nm). This result highlights that Titan's surface remains active despite the absorption of the most energetic photons by the atmosphere.AcknowledgmentsThis work is supported by NASA Solar System Workings grant " Photochemistry in Titan's Lower Atmosphere". The research work has been carried out at the Jet Propulsion Laboratory, California Institute of Technology under a contract with the National Aeronautics and Space Administration. NC acknowledges the European Research Council for their financial support (ERC Starting Grant PRIMCHEM, grant agreement n°636829).References[1] Waite, J. H., et al., The process of Tholin formation in Titan's upper atmosphere, (2007), Science 316, 870-875.[2] Fulchignoni, M., et al., In situ measurements of the physical characteristics of Titan's environment, (2005), Nature 438, 785-791[3] Lavvas, P., et al., Condensation in Titan's atmosphere at the Huygens landing site, (2011), Icarus 215, 732-750.

  18. Appearance of strong absorbers and fluorophores in limonene-O3 secondary organic aerosol due to NH4+-mediated chemical aging over long time scales

    NASA Astrophysics Data System (ADS)

    Bones, David L.; Henricksen, Dana K.; Mang, Stephen A.; Gonsior, Michael; Bateman, Adam P.; Nguyen, Tran B.; Cooper, William J.; Nizkorodov, Sergey A.

    2010-03-01

    This study investigated long-term chemical aging of model biogenic secondary organic aerosol (SOA) prepared from the ozonolysis of terpenes. Techniques including electrospray ionization mass spectrometry (ESI-MS), UV-visible spectroscopy, Fourier transform infrared (FTIR) spectroscopy, NMR, and three-dimensional fluorescence were used to probe the changes in chemical composition of SOA collected by impaction on substrates and also of aqueous extracts of SOA. The addition of ammonium ions or amino acids to limonene SOA reproducibly produced orange-colored species that strongly absorbed visible radiation and fluoresced at UV and visible wavelengths. Simultaneous addition of H2SO4 to the SOA aqueous extracts inhibited this color transformation. These observations suggest the existence of aging processes leading to heavily conjugated molecules containing organic nitrogen. The presence of nitrogen in the chromophores was confirmed by the dependence of the absorption and fluorescence spectra on the amino acids added. In contrast to the strong change in the absorption and fluorescence spectra, there was no significant change in the ESI-MS, FTIR, and NMR spectra, suggesting that the chromophores were minor species in the aged SOA. Aqueous extracts of aged limonene + NH4+ SOA were characterized by an effective base-e absorption coefficient of ˜3 L g-1 cm-1 at 500 nm. Assuming particulate matter concentrations typical of polluted rural air gives an upper limit of 0.2 M m-1 for the aerosol absorption coefficient due to the aged limonene oxidation products. Biogenic SOA can therefore become weakly absorbing if they undergo aging in the presence of NH4+-containing aerosol.

  19. Reactive Oxygen Species in Combustion Aerosols

    NASA Astrophysics Data System (ADS)

    Balasubramanian, R.; See, S.

    2007-12-01

    Research on airborne particulate matter (PM) has received increased concern in recent years after it was identified as a major component of the air pollution mix that is strongly associated with premature mortality and morbidity. Particular attention has been paid to understanding the potential health impacts of fine particles (PM2.5), which primarily originate from combustion sources. One group of particulate-bound chemical components of health concern is reactive oxygen species (ROS), which include molecules such as hydrogen peroxide (H2O2), ions such as hypochlorite ion (OCl-), free radicals such as hydroxyl radical (·OH) and superoxide anion (·O2-) which is both an ion and a radical. However, the formation of ROS in PM is not clearly understood yet. Furthermore, the concentration of ROS in combustion particles of different origin has not been quantified. The primary objective of this work is to study the effect of transition metals on the production of ROS in PM2.5 by determining the concentrations of ROS and metals. Both soluble and total metals were measured to evaluate their respective associations with ROS. PM2.5 samples were collected from several outdoor and indoor combustion sources, including those emitted from on-road vehicles, food cooking, incense sticks, and cigarette smoke. PM2.5 samples were also collected from the background air in both the ambient outdoor and indoor environments to assess the levels of particulate-bound transition metals and ROS with no combustion activities in the vicinity of sampling locations. Results obtained from this comprehensive study on particulate-bound ROS will be presented and discussed.

  20. Models for the optical simulations of fractal aggregated soot particles thinly coated with non-absorbing aerosols

    NASA Astrophysics Data System (ADS)

    Wu, Yu; Cheng, Tianhai; Zheng, Lijuan; Chen, Hao

    2016-10-01

    Light absorption enhancement of aged soot aerosols is highly sensitive to the morphologies and mixing states of soot aggregates and their non-absorbing coatings, such as organic materials. The quantification of these effects on the optical properties of thinly coated soot aerosols is simulated using an effective model with fixed volume fractions. Fractal aggregated soot was simulated using the diffusion limited aggregation (DLA) algorithm and discretized into soot dipoles. The dipoles of non-absorbing aerosols, whose number was fixed by the volume fraction, were further generated from the neighboring random edge dipoles. Their optical properties were calculated using the discrete dipole approximation (DDA) method and were compared with other commonly used models. The optical properties of thinly coated soot calculated using the fixed volume fraction model are close to (less than ~10% difference) the results of the fixed coating thickness model, except their asymmetry parameters (up to ~25% difference). In the optical simulations of thinly coated soot aerosols, this relative difference of asymmetry parameters and phase functions between these realistic models may be notable. The realizations of the fixed volume fraction model may introduce smaller variation of optical results than those of the fixed coating thickness model. Moreover, the core-shell monomers model and homogeneous aggregated spheres model with the Maxwell-Garnett (MG) theory may underestimate (up to ~20%) the cross sections of thinly coated soot aggregates. The single core-shell sphere model may largely overestimate (up to ~150%) the cross sections and single scattering albedo of thinly coated soot aggregates, and it underestimated (up to ~60%) their asymmetry parameters. It is suggested that the widely used single core-shell sphere approximation may not be suitable for the single scattering calculations of thinly coated soot aerosols.

  1. Measurements of Absorbing Aerosols Using in Situ and Remote Sensing Techniques

    NASA Astrophysics Data System (ADS)

    Martins, J. V.; Martins, J. V.; Kaufman, Y.; Artaxo, P.; Andrea, C.; Yamasoe, M.; Remer, L.

    2001-12-01

    Reliable measurements of light absorption by aerosol particles are essential for an accurate assessment of the climate radiative forcing by aerosol particles. Depending on the absorption properties, the radiative forcing of the aerosols may change from a cooling to a heating effect. New techniques for the remote sensing of aerosol absorption over land and ocean are developed and applied in combination with in situ measurements for validation and addition of complementary information. Spectral measurements show the effects of aerosols on absorption of light from the UV to the near infrared. Depending on particle size and structure, there is a significant absorption component that must be accounted for the radiative forcing in the near infrared. Remote sensing results from MODIS and from the CLAMS field experiment, as well as in situ validation data will be discussed.

  2. The relationship of boundary layer clouds in the tropical southeast Atlantic to absorbing aerosols, meteorology and climate change

    NASA Astrophysics Data System (ADS)

    Zuidema, P.; Adebiyi, A. A.; Ramajiguru, L.

    2015-12-01

    Ascension Island, a remote island located in the middle of the Atlantic Ocean within the trade-wind region oat 8S, 14.5W, experiences the outflow of biomass-burning aerosols from continental Africa, over 2000 km away, from July through November, peaking in August and September. The shortwave-absorbing free-tropospheric aerosols, located in a region of high solar irradiance, provide a climate warming that is poorly represented in global aerosol climate models. The low clouds can respond to the smoke layer in myriad possible ways that are not yet well-documented. The shortwave-warming can stabilize the free-troposphere, enhancing the low cloud fraction. The deepening boundary layer and subsiding smoke layer also increase the likelihood of aerosol-cloud microphysical interactions. Interest in this climate regime is supporting an observational strategy of a year-long DOE ARM Mobile Facility deployment to Ascension (Layered Atlantic Smoke Interactions with Clouds, or LASIC), and an NSF aircraft campaign (ObservatioNs of Fire's Impact on the southeast atlantic REgion, or ONFIRE) based on Sao Tome Island. These campaigns will be integrated with NASA, UK and African activities sharing similar goals based further south in Namibia. Initial analysis is distinguishing meteorology from aerosol impacts on the boundary layer cloud fields. The forward trajectories of emissions from over 24,000 fire sources on continental Africa show that a free-tropospheric jet can advect aerosols to above Ascension island in just one-two days. The fast transport time encourages retention of signatures of the fire sources, in particular the radiatively-crucial single-scattering albedo value. Thereafter, a deep land-based anticyclonic high recirculates over one-third of these trajectories back to the African continent, explaining the widespread extent of the aerosol layer. The free-tropospheric jet also reduces the mean atmospheric subsidence independently of shortwave absorption by the aerosols

  3. Development of a sensitive long pathlength absorbance photometer to quantify peroxides in aerosol particles (Peroxide-LOPAP)

    NASA Astrophysics Data System (ADS)

    Mertes, P.; Pfaffenberger, L.; Dommen, J.; Kalberer, M.; Baltensperger, U.

    2012-02-01

    A new off-line instrument to quantify peroxides in aerosol particles using iodometry in long pathlength absorption spectroscopy has been developed and is called peroxide long pathlength absorbance photometer (Peroxide-LOPAP). The new analytical setup features important technical innovations compared to hitherto published iodometric peroxide measurements. Firstly, the extraction, chemical conversion and measurement of the aerosol samples are performed in a closed oxygen-free (∼1 ppb) environment. Secondly, a 50-cm optical detection cell is used for an increased photometric sensitivity. The limit of detection was 0.1 μM peroxide in solution or 0.25 nmol m-3 with respect to an aerosol sample volume of 1000 l. The test reaction was done at a constant elevated temperature of 40 °C and the reaction time was 60 min. Calibration experiments showed that the test reaction with all reactive peroxides, i.e. hydrogen peroxide (H2O2), peracids and peroxides with vicinal carbonyl groups (e.g. lauroyl peroxide) goes to completion and their sensitivity (slope of calibration curve) varies by only ±5%. However, very stable peroxides have a lower sensitivity. For example tert-butyl hydroperoxide shows only 37% sensitivity compared to H2O2 after 1h. A kinetic study revealed that even after 5 h only 85% of this stable compound had reacted. The time trends of the peroxide content in secondary organic aerosol (SOA) from the ozonolysis and photo-oxidation of α-pinene in smog chamber experiments were measured. The highest amount of peroxides with 34% (assuming a MW of 300 g mol-1) was found in freshly generated SOA from α-pinene ozonolysis. Contents decreased with increasing NO levels in the photo-oxidation experiments. A decrease of the peroxide content was observed with aging of the aerosol indicating a decomposition of peroxides in the particles.

  4. Soluble, light-absorbing species in snow at Barrow, Alaska

    NASA Astrophysics Data System (ADS)

    Beine, Harry; Anastasio, Cort; Esposito, Giulio; Patten, Kelley; Wilkening, Elizabeth; Domine, Florent; Voisin, Didier; Barret, Manuel; Houdier, Stephan; Hall, Sam

    2011-07-01

    As part of the international multidisciplinary Ocean - Atmosphere - Sea Ice - Snowpack (OASIS) program we analyzed more than 500 terrestrial (melted) snow samples near Barrow, AK between February and April 2009 for light absorption, as well as H2O2 and inorganic anion concentrations. For light absorption in the photochemically active region (300-450 nm) of surface snows, H2O2 and NO3- make minor contributions (combined < 9% typically), while HUmic LIke Substances (HULIS) and unknown chromophores each account for approximately half of the total absorption. We have identified four main sources for our residual chromophores (i.e., species other than H2O2 or NO3-): (1) vegetation and organic debris impact mostly the lowest 20 cm of the snowpack, (2) marine inputs, which are identified by high Cl- and SO42- contents, (3) deposition of diamond dust to surface snow, and (4) gas-phase exchange between the atmosphere and surface snow layers. The snow surfaces, and accompanying chromophore concentrations, are strongly modulated by winds and snowfall at Barrow. However, even with these physical controls on light absorption, we see an overall decline of light absorption in near-surface snow during the 7 weeks of our campaign, likely due to photo-bleaching of chromophores. While HULIS and unknown chromophores dominate light absorption by soluble species in Barrow snow, we know little about the photochemistry of these species, and thus we as a community are probably overlooking many snowpack photochemical reactions.

  5. Two chemically distinct light-absorbing pools of urban organic aerosols: A comprehensive multidimensional analysis of trends.

    PubMed

    Paula, Andreia S; Matos, João T V; Duarte, Regina M B O; Duarte, Armando C

    2016-02-01

    The chemical and light-absorption dynamics of organic aerosols (OAs), a master variable in the atmosphere, have yet to be resolved. This study uses a comprehensive multidimensional analysis approach for exploiting simultaneously the compositional changes over a molecular size continuum and associated light-absorption (ultraviolet absorbance and fluorescence) properties of two chemically distinct pools of urban OAs chromophores. Up to 45% of aerosol organic carbon (OC) is soluble in water and consists of a complex mixture of fluorescent and UV-absorbing constituents, with diverse relative abundances, hydrophobic, and molecular weight (Mw) characteristics between warm and cold periods. In contrast, the refractory alkaline-soluble OC pool (up to 18%) is represented along a similar Mw and light-absorption continuum throughout the different seasons. Results suggest that these alkaline-soluble chromophores may actually originate from primary OAs sources in the urban site. This work shows that the comprehensive multidimensional analysis method is a powerful and complementary tool for the characterization of OAs fractions. The great diversity in the chemical composition and optical properties of OAs chromophores, including both water-soluble and alkaline-soluble OC, may be an important contribution to explain the contrasting photo-reactivity and atmospheric behavior of OAs.

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

    NASA Astrophysics Data System (ADS)

    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

  7. Light-absorbing soluble organic aerosol in Los Angeles and Atlanta: A contrast in secondary organic aerosol

    NASA Astrophysics Data System (ADS)

    Zhang, Xiaolu; Lin, Ying-Hsuan; Surratt, Jason D.; Zotter, Peter; Prévôt, Andre S. H.; Weber, Rodney J.

    2011-11-01

    Light absorption spectra and carbon mass of fine particle water-soluble components were measured during the summer of 2010 in the Los Angeles (LA) basin, California, and Atlanta, Georgia. Fresh LA secondary organic carbon had a consistent brown color and a bulk absorption per soluble carbon mass at 365 nm that was 4 to 6 times higher than freshly-formed Atlanta soluble organic carbon. Radiocarbon measurements of filter samples show that LA secondary organic aerosol (SOA) was mainly from fossil carbon and chemical analysis of aqueous filter extracts identified nitro-aromatics as one component of LA brown SOA. Interpreting soluble brown carbon as a property of freshly-formed anthropogenic SOA, the difference in absorption per carbon mass between these two cities suggests most fresh secondary water-soluble organic carbon formed within Atlanta is not from an anthropogenic process similar to LA. Contrasting emissions of biogenic volatile organic compounds may account for these differences.

  8. Absorbing and scattering aerosols over the source region of biomass burning emissions: Implications in the assessment of optical and radiative properties

    NASA Astrophysics Data System (ADS)

    Singh, Atinderpal; Srivastava, Rohit; Rastogi, Neeraj; Singh, Darshan

    2016-02-01

    The current study focuses on the assessment of model simulated optical and radiative properties of aerosols incorporating the measured chemical composition of aerosol samples collected at Patiala during October, 2011-February, 2012. Monthly average mass concentration of PM2.5, elemental carbon (EC), primary organic carbon (POC), water-soluble (WS) and insoluble (INS) aerosols ranged from 120 to 192, 6.2 to 7.2, 20 to 39, 59 to 111 and 35 to 90 μg m-3, respectively. Mass concentration of different components of aerosols was further used for the assessment of optical properties derived from Optical Properties of Aerosols and Clouds (OPAC) model simulations. Microtops based measured aerosol optical depth (AOD500) ranged from 0.47 to 0.62 showing maximum value during November and December, and minimum during February. Ångström exponent (α380-870) remained high (>0.90) throughout the study period except in February (0.74), suggesting predominance of fine mode particles over the study region. The observed ratio of scattering to absorbing aerosols was incorporated in OPAC model simulations and single scattering albedo (SSA at 500 nm) so obtained ranged between 0.80 and 0.92 with relatively low values during the period of extensive biomass burning. In the present study, SBDART based estimated values of aerosol radiative forcing (ARF) at the surface (SRF) and top of the atmosphere (TOA) ranged from -31 to -66 Wm-2 and -2 to -18 W m-2 respectively. The atmospheric ARF, ranged between + 18 and + 58 Wm-2 resulting in the atmospheric heating rate between 0.5 and 1.6 K day-1. These results signify the role of scattering and absorbing aerosols in affecting the magnitude of aerosol forcing.

  9. Condensational growth and trace species scavenging in stratospheric sulfuric acid/water aerosol droplets

    NASA Technical Reports Server (NTRS)

    Tompson, Robert V., Jr.

    1991-01-01

    Stratospheric aerosols play a significant role in the environment. The composition of aerosols is believed to be a liquid solution of sulfuric acid and water with numerous trace species. Of these trace species, ozone in particular was recognized as being very important in its role of shielding the environment from harmful ultraviolet radiation. Also among the trace species are HCl and ClONO2, the so called chlorine reservoir species and various oxides of nitrogen. The quantity of stratospheric aerosol and its particle size distribution determines, to a large degree, the chemistry present in the stratosphere. Aerosols experience 3 types of growth: nucleation, condensation, and coagulation. The application of condensation investigations to the specific problem of stratospheric aerosols is discussed.

  10. Effects of absorbing aerosols on accelerated melting of snowpack in the Hindu-Kush-Himalayas-Tibetan Plateau region

    NASA Astrophysics Data System (ADS)

    Lau, W. K.; Kim, K.; Yasunari, T. J.; Gautam, R.; Hsu, N. C.

    2011-12-01

    The impacts of absorbing aerosol on melting of snowpack in the Hindu-Kush-Himalayas-Tibetan Plateau (HKHT) region are studied using in-situ, satellite observations, and GEOS-5 GCM. Based on atmospheric black carbon measurements from the Pyramid observation (~ 5 km elevation) in Mt. Everest, we estimate that deposition of black carbon on snow surface will give rise to a reduction in snow surface albedo of 2- 5 %, and an increased annual runoff of 12-34% for a typical Tibetan glacier. Examination of multi-year satellite reflectivity and re-analysis data reveals signals of possible impacts of dust and black carbon in darkening the snow surface, and accelerating spring melting of snowpack in the HKHT, following a build-up of absorbing aerosols in the Indo-Gangetic Plain. Results from GCM experiments show that a 8-10% increase in the rate of melting of snowpack over the western Himalayas and Tibetan Plateau can be attributed to the elevated-heat-pump (EHP) feedback effect, initiated from the absorption of solar radiation by dust and black carbon accumulated to great height (~ 5 km) over the Indo-Gangetic Plain and Himalayas foothills in the pre-monsoon season (April-May). The accelerated melting of the snowpack is enabled by an EHP-induced atmosphere-land-snowpack positive feedback involving a) orographic forcing of the monsoon flow by the complex terrain of the HKHT region, leading to increased moisture, cloudiness and rainfall over the Himalayas foothills and northern India, b) warming of the upper troposphere over the Tibetan Plateau, and c) a transfer of latent and sensible heat from atmosphere to the snow surface. Ongoing modeling work in assessing the relative roles of EHP vs. snow-darkening effects on accelerated melting of snowpack in HKHT region will be discussed.

  11. Effects of Absorbing Aerosols on Accelerated Melting of Snowpack in the Hindu-Kush-Himalayas-Tibetan Plateau Region

    NASA Technical Reports Server (NTRS)

    Lau, William K.; Kyu-Myong, Kim; Yasunari, Teppei; Gautam, Ritesh; Hsu, Christina

    2011-01-01

    The impacts of absorbing aerosol on melting of snowpack in the Hindu-Kush-Himalayas-Tibetan Plateau (HKHT) region are studied using in-situ, satellite observations, and GEOS-5 GCM. Based on atmospheric black carbon measurements from the Pyramid observation ( 5 km elevation) in Mt. Everest, we estimate that deposition of black carbon on snow surface will give rise to a reduction in snow surface albedo of 2- 5 %, and an increased annual runoff of 12-34% for a typical Tibetan glacier. Examination of satellite reflectivity and re-analysis data reveals signals of possible impacts of dust and black carbon in darkening the snow surface, and accelerating spring melting of snowpack in the HKHT, following a build-up of absorbing aerosols in the Indo-Gangetic Plain. Results from GCM experiments show that 8-10% increase in the rate of melting of snowpack over the western Himalayas and Tibetan Plateau can be attributed to the elevated-heat-pump (EHP) feedback effect, initiated from the absorption of solar radiation by dust and black carbon accumulated to great height ( 5 km) over the Indo-Gangetic Plain and Himalayas foothills in the pre-monsoon season (April-May). The accelerated melting of the snowpack is enabled by an EHP-induced atmosphere-land-snowpack positive feedback involving a) orographic forcing of the monsoon flow by the complex terrain, and thermal forcing of the HKHT region, leading to increased moisture, cloudiness and rainfall over the Himalayas foothills and northern India, b) warming of the upper troposphere over the Tibetan Plateau, and c) an snow albedo-temperature feedback initiated by a transfer of latent and sensible heat from a warmer atmosphere over the HKHT to the underlying snow surface. Results from ongoing modeling work to assess the relative roles of EHP vs. snow-darkening effects on accelerated melting of snowpack in HKHT region will also be discussed.

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

    NASA Technical Reports Server (NTRS)

    Portscht, R.

    1977-01-01

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

  13. Estimate of the Impact of Absorbing Aerosol Over Cloud on the MODIS Retrievals of Cloud Optical Thickness and Effective Radius Using Two Independent Retrievals of Liquid Water Path

    NASA Technical Reports Server (NTRS)

    Wilcox, Eric M.; Harshvardhan; Platnick, Steven

    2009-01-01

    Two independent satellite retrievals of cloud liquid water path (LWP) from the NASA Aqua satellite are used to diagnose the impact of absorbing biomass burning aerosol overlaying boundary-layer marine water clouds on the Moderate Resolution Imaging Spectrometer (MODIS) retrievals of cloud optical thickness (tau) and cloud droplet effective radius (r(sub e)). In the MODIS retrieval over oceans, cloud reflectance in the 0.86-micrometer and 2.13-micrometer bands is used to simultaneously retrieve tau and r(sub e). A low bias in the MODIS tau retrieval may result from reductions in the 0.86-micrometer reflectance, which is only very weakly absorbed by clouds, owing to absorption by aerosols in cases where biomass burning aerosols occur above water clouds. MODIS LWP, derived from the product of the retrieved tau and r(sub e), is compared with LWP ocean retrievals from the Advanced Microwave Scanning Radiometer-EOS (AMSR-E), determined from cloud microwave emission that is transparent to aerosols. For the coastal Atlantic southern African region investigated in this study, a systematic difference between AMSR-E and MODIS LWP retrievals is found for stratocumulus clouds over three biomass burning months in 2005 and 2006 that is consistent with above-cloud absorbing aerosols. Biomass burning aerosol is detected using the ultraviolet aerosol index from the Ozone Monitoring Instrument (OMI) on the Aura satellite. The LWP difference (AMSR-E minus MODIS) increases both with increasing tau and increasing OMI aerosol index. During the biomass burning season the mean LWP difference is 14 g per square meters, which is within the 15-20 g per square meter range of estimated uncertainties in instantaneous LWP retrievals. For samples with only low amounts of overlaying smoke (OMI AI less than or equal to 1) the difference is 9.4, suggesting that the impact of smoke aerosols on the mean MODIS LWP is 5.6 g per square meter. Only for scenes with OMI aerosol index greater than 2 does the

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

    PubMed Central

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

    2014-01-01

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

  15. Estimating the Direct Radiative Effect of Absorbing Aerosols Overlying Marine Boundary Layer Clouds in the Southeast Atlantic Using MODIS and CALIOP

    NASA Technical Reports Server (NTRS)

    Meyer, Kerry; Platnick, Steven; Oreopoulos, Lazaros; Lee, Dongmin

    2013-01-01

    Absorbing aerosols such as smoke strongly absorb solar radiation, particularly at ultraviolet and visible/near-infrared (VIS/NIR) wavelengths, and their presence above clouds can have considerable implications. It has been previously shown that they have a positive (i.e., warming) direct aerosol radiative effect (DARE) when overlying bright clouds. Additionally, they can cause biased passive instrument satellite retrievals in techniques that rely on VIS/NIR wavelengths for inferring the cloud optical thickness (COT) and effective radius (re) of underlying clouds, which can in turn yield biased above-cloud DARE estimates. Here we investigate Moderate Resolution Imaging Spectroradiometer (MODIS) cloud optical property retrieval biases due to overlying absorbing aerosols observed by Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP) and examine the impact of these biases on above-cloud DARE estimates. The investigation focuses on a region in the southeast Atlantic Ocean during August and September (2006-2011), where smoke from biomass burning in southern Africa overlies persistent marine boundary layer stratocumulus clouds. Adjusting for above-cloud aerosol attenuation yields increases in the regional mean liquid COT (averaged over all ocean-only liquid clouds) by roughly 6%; mean re increases by roughly 2.6%, almost exclusively due to the COT adjustment in the non-orthogonal retrieval space. It is found that these two biases lead to an underestimate of DARE. For liquid cloud Aqua MODIS pixels with CALIOP-observed above-cloud smoke, the regional mean above-cloud radiative forcing efficiency (DARE per unit aerosol optical depth (AOD)) at time of observation (near local noon for Aqua overpass) increases from 50.9Wm(sup-2)AOD(sup-1) to 65.1Wm(sup-2)AOD(sup -1) when using bias-adjusted instead of nonadjusted MODIS cloud retrievals.

  16. Seasonal variations in the light-absorbing properties of water-soluble and insoluble organic aerosols in Seoul, Korea

    NASA Astrophysics Data System (ADS)

    Kim, Hwajin; Kim, Jin Young; Jin, Hyoun Cher; Lee, Ji Yi; Lee, Se Pyo

    2016-03-01

    The spectral properties of light-absorbing organic aerosol extractions were investigated using 24-h average fine particulate matter (PM2.5) measurements from October 2012 to September 2013 in Seoul, Korea. The light-absorption spectra of water and methanol extracts exhibited strong evidence of brown carbon with Absorption Angstrom Exponent (AAE; fitted between 300 and 700 nm) ranges of 5.84-9.17 and 4.08-5.75, with averages of 7.23 ± 1.58 and 5.05 ± 0.67, respectively. The light absorption of both extracts at 365 nm (Abs365), which is typically used as a proxy for brown carbon (BrC), displayed strong seasonal variations and was well correlated with both water-soluble organic carbon (WSOC; r = 0.81) and organic carbon (OC; r = 0.85), indicating that both primary and secondary organics were sources of BrC in this region. Normalizing the Abs365 of water and methanol extracts to the mass of WSOC and OC yielded average solution mass absorption efficiency (MAE365) of 0.28-1.18 and 0.44-1.45 m2 g-1 C, respectively. MAE365 in Korea were in the same range or slightly lower than those in China, however, despite the same ranges, the seasonal variations were different, suggesting that the sources of light absorbers could be different. Combining the AAE, Abs365, and MAE365 of both extracts and a detailed chemical speciation of filter extracts identified the compounds responsible for the temporal variations of BrC in Korea. During summer, secondary organic aerosol (SOA), photochemically generated from anthropogenic emissions, was the major source; however, during winter, long range transported organics or transported BrC seem to be a source of BrC in Korea, a downwind site of China, where severe smog and BrC were observed during this season. Biomass burning was also an important source; however, unlike in previous studies, where it was identified as a major source during winter, here, it contributed during the whole year. Although many of its properties, sources, and potential

  17. Aerosols

    Atmospheric Science Data Center

    2013-04-17

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

  18. Two-photon or higher-order absorbing optical materials for generation of reactive species

    NASA Technical Reports Server (NTRS)

    Cumpston, Brian (Inventor); Lipson, Matthew (Inventor); Marder, Seth R (Inventor); Perry, Joseph W (Inventor)

    2007-01-01

    Disclosed are highly efficient multiphoton absorbing compounds and methods of their use. The compounds generally include a bridge of pi-conjugated bonds connecting electron donating groups or electron accepting groups. The bridge may be substituted with a variety of substituents as well. Solubility, lipophilicity, absorption maxima and other characteristics of the compounds may be tailored by changing the electron donating groups or electron accepting groups, the substituents attached to or the length of the pi-conjugated bridge. Numerous photophysical and photochemical methods are enabled by converting these compounds to electronically excited states upon simultaneous absorption of at least two photons of radiation. The compounds have large two-photon or higher-order absorptivities such that upon absorption, one or more Lewis acidic species, Lewis basic species, radical species or ionic species are formed.

  19. Two-Photon or Higher-Order Absorbing Optical Materials for Generation of Reactive Species

    NASA Technical Reports Server (NTRS)

    Cumpston, Brian (Inventor); Lipson, Matthew (Inventor); Marder, Seth R. (Inventor); Perry, Joseph W. (Inventor)

    2013-01-01

    Disclosed are highly efficient multiphoton absorbing compounds and methods of their use. The compounds generally include a bridge of pi-conjugated bonds connecting electron donating groups or electron accepting groups. The bridge may be substituted with a variety of substituents as well. Solubility, lipophilicity, absorption maxima and other characteristics of the compounds may be tailored by changing the electron donating groups or electron accepting groups, the substituents attached to or the length of the pi-conjugated bridge. Numerous photophysical and photochemical methods are enabled by converting these compounds to electronically excited states upon simultaneous absorption of at least two photons of radiation. The compounds have large two-photon or higher-order absorptivities such that upon absorption, one or more Lewis acidic species, Lewis basic species, radical species or ionic species are formed.

  20. Two-photon or higher-order absorbing optical materials for generation of reactive species

    NASA Technical Reports Server (NTRS)

    Cumpston, Brian (Inventor); Lipson, Matthew (Inventor); Marder, Seth R. (Inventor); Perry, Joseph W. (Inventor)

    2003-01-01

    Disclosed are highly efficient multiphoton absorbing compounds and methods of their use. The compounds generally include a bridge of pi-conjugated bonds connecting electron donating groups or electron accepting groups. The bridge may be substituted with a variety of substituents as well. Solubility, lipophilicity, absorption maxima and other characteristics of the compounds may be tailored by changing the electron donating groups or electron accepting groups, the substituents attached to or the length of the pi-conjugated bridge. Numerous photophysical and photochemical methods are enabled by converting these compounds to electronically excited states upon simultaneous absorption of at least two photons of radiation. The compounds have large two-photon or higher-order absorptivities such that upon absorption, one or more Lewis acidic species, Lewis basic species, radical species or ionic species are formed.

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

    PubMed

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

    2013-01-01

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

  2. Calibration method for a photoacoustic system for real time source apportionment of light absorbing carbonaceous aerosol based on size distribution measurements

    NASA Astrophysics Data System (ADS)

    Utry, Noemi; Ajtai, Tibor; Pinter, Mate; Orvos, Peter I.; Szabo, Gabor; Bozoki, Zoltan

    2016-04-01

    In this study, we introduce a calibration method with which sources of light absorbing carbonaceous particulate matter (LAC) can be apportioned in real time based on multi wavelength optical absorption measurements with a photoacoustic system. The method is primary applicable in wintry urban conditions when LAC is dominated by traffic and biomass burning. The proposed method was successfully tested in a field campaign in the city center of Szeged, Hungary during winter time where the dominance of traffic and wood burning aerosol has been experimentally demonstrated earlier. With the help of the proposed calibration method a relationship between the measured Aerosol Angström Exponent (AAE) and the number size distribution can be deduced. Once the calibration curve is determined, the relative strength of the two pollution sources can be deduced in real time as long as the light absorbing fraction of PM is exclusively related to traffic and wood burning. This assumption is indirectly confirmed in the presented measurement campaign by the fact that the measured size distribution is composed of two unimodal size distributions identified to correspond to traffic and wood burning aerosols. The proposed method offers the possibility of replacing laborious chemical analysis with simple in-situ measurement of aerosol size distribution data.

  3. Formation of nitrogen- and sulfur-containing light-absorbing compounds accelerated by evaporation of water from secondary organic aerosols

    NASA Astrophysics Data System (ADS)

    Nguyen, Tran B.; Lee, Paula B.; Updyke, Katelyn M.; Bones, David L.; Laskin, Julia; Laskin, Alexander; Nizkorodov, Sergey A.

    2012-01-01

    Aqueous extracts of secondary organic aerosols (SOA) generated from the ozonolysis of d-limonene were subjected to dissolution, evaporation, and re-dissolution in the presence and absence of ammonium sulfate (AS). Evaporation with AS at pH 4-9 produced chromophores that were stable with respect to hydrolysis and had a distinctive absorption band at 500 nm. Evaporation accelerated the rate of chromophore formation by at least three orders of magnitude compared to the reaction in aqueous solution, which produced similar compounds. Absorption spectroscopy and high-resolution nanospray desorption electrospray ionization (nano-DESI) mass spectrometry experiments suggested that the molar fraction of the chromophores was small (<2%), and that they contained nitrogen atoms. Although the colored products represented only a small fraction of SOA, their large extinction coefficients (>105 L mol-1 cm-1 at 500 nm) increased the effective mass absorption coefficient of the residual organics in excess of 103 cm2 g-1 - a dramatic effect on the optical properties from minor constituents. Evaporation of SOA extracts in the absence of AS resulted in the production of colored compounds only when the SOA extract was acidified to pH ˜ 2 with sulfuric acid. These chromophores were produced by acid-catalyzed aldol condensation, followed by a conversion into organosulfates. The presence of organosulfates was confirmed by high resolution mass spectrometry experiments. Results of this study suggest that evaporation of cloud or fog droplets containing dissolved organics leads to significant modification of the molecular composition and serves as a potentially important source of light-absorbing compounds.

  4. Formation of Nitrogen- and Sulfur-Containing Light-Absorbing Compounds Accelerated by Evaporation of Water from Secondary Organic Aerosols

    SciTech Connect

    Nguyen, Tran B.; Lee, Paula B.; Updyke, Katelyn M.; Bones, David L.; Laskin, Julia; Laskin, Alexander; Nizkorodov, Sergey

    2012-01-14

    Aqueous extracts of secondary organic aerosols (SOA) generated from the ozonolysis of dlimonene were subjected to dissolution, evaporation, and re-dissolution in the presence and absence of ammonium sulfate (AS). Evaporation with AS at pH 4-9 produced chromophores that were stable with respect to hydrolysis and had a distinctive absorption band at 500 nm. Evaporation accelerated the rate of chromophore formation by at least three orders of magnitude compared to the reaction in aqueous solution, which produced similar compounds. Absorption spectroscopy and high-resolution nanospray desorption electrospray ionization (nano-DESI) mass spectrometry experiments suggested that the molar fraction of the chromophores was small (< 2%), and that they contained nitrogen atoms. Although the colored products represented only a small fraction of SOA, their large extinction coefficients (>10{sup 5} L mol{sup -1} cm{sup -1} at 500 nm) increased the effective mass absorption coefficient of the residual organics in excess of 10{sup 3} cm{sup 2} g{sup -1} - a dramatic effect on the optical properties from minor constituents. Evaporation of SOA extracts in the absence of AS resulted in the production of colored compounds only when the SOA extract was acidified to pH {approx} 2 with sulfuric acid. These chromophores were produced by acid-catalyzed aldol condensation, followed by a conversion into organosulfates. The presence of organosulfates was confirmed by high resolution mass spectrometry experiments. Results of this study suggest that evaporation of cloud or fog droplets containing dissolved organics leads to significant modification of the molecular composition and serves as a potentially important source of light-absorbing compounds.

  5. Possible combined influences of absorbing aerosols and anomalous atmospheric circulation on summertime diurnal temperature range variation over the middle and lower reaches of the Yangtze River

    NASA Astrophysics Data System (ADS)

    Cai, Jiaxi; Guan, Zhaoyong; Ma, Fenhua

    2016-12-01

    Based on the temperature data from the China Meteorological Administration, NCEP-NCAR reanalysis data, and the TOMS Aerosol Index (AI), we analyze the variations in the summertime diurnal temperature range (DTR) and temperature maxima in the middle and lower reaches of the Yangtze River (MLRYR) in China. The possible relationships between the direct warming effect of the absorbing aerosol and temperature variations are further investigated, although with some uncertainties. It is found that the summertime DTR exhibits a decreasing trend over the most recent 50 years, along with a slight increasing tendency since the 1980s. The trend of the maximum temperature is in agreement with those of the DTR and the absorbing aerosols. To investigate the causes of the large anomalies in the temperature maxima, composite analyses of the circulation anomalies are performed. When anomalous AI and anomalous maximum temperature over the MLRYR have the same sign, an anomalous circulation with a quasi-barotropic structure occurs there. This anomalous circulation is modulated by the Rossby wave energy propagations from the regions northwest of the MLRYR and influences the northwestern Pacific subtropical high over the MLRYR. In combination with aerosols, the anomalous circulation may increase the maximum temperature in this region. Conversely, when the anomalous AI and anomalous maximum temperature in the MLRYR have opposite signs, the anomalous circulation is not equivalently barotropic, which possibly offsets the warming effect of aerosols on the maximum temperature changes in this region. These results are helpful for a better understanding of the DTR changes and the occurrences of temperature extremes in the MLRYR region during boreal summer.

  6. Four dimensional variational data assimilation of species-resolved satellite-retrieved aerosol optical thickness

    NASA Astrophysics Data System (ADS)

    Nieradzik, Lars Peter; Elbern, Hendrik

    2010-05-01

    Aerosols play an increasingly important role in atmospheric modelling. They have a strong influence on the radiative transfer balance and a significant impact on human health. Their origin is various and so are its effects. Most of the measurement sites in Europe only account for an integrated aerosol load PMx (Particulate Matter of less than x μm in diameter) which does not give any qualitative information on the composition of the aerosol. Since very different constituents like mineral dust derived from desert storms and sea salt contribute to PMx it is necessary to make aerosol forcasts not only of load, but also type resolved. The source of information chosen for this study is the aerosol retrieval system SYNAER (SYNergetic AErosol Retrieval) from DLR-DFD that retrieves BLAOT (Boundary Layer Aerosol Optical Thickness) making use of both AATSR/SCIAMACHY and AVHRR/GOME-2 data respectively. Its strengths are a large spatial coverage, near real-time availability, and the classification of five intrinsic aerosol species, namely water-solubles, water-insolubles, soot, sea salt, and mineral dust which are furthermore size resolved in terms of modes. A widely known technique to enhance forecast skills of CTMs (Chemistry-Transport-Models) by ingesting in-situ and, especially, remote-sensing measurements is the method of four dimensional variational data assimilation (4Dvar). The EURAD-IM (EURopean Air pollution Dispersion - Inverse Model), containing a full adjoint gas-phase model, has been expanded with an adjoint of the MADE (Modal Aerosol Dynamics model for Europe) to optimise initial and boundary values for aerosols using 4Dvar. A forward and an adjoint radiative transfer model is driven by the EURAD-IM as mapping between BLAOT and internal aerosol species. Furthermore, its condensation scheme has been bypassed by an HDMR (High-Dimensional-Model-Representation) to ensure differentiability, and a time saving online NMC-module for the generation of the background

  7. Local and remote impacts of aerosol species on Indian summer monsoon rainfall in a GCM

    NASA Astrophysics Data System (ADS)

    Guo, Liang; Turner, Andrew; Highwood, Eleanor

    2016-04-01

    The HadGEM2 AGCM is used to determine the most important anthropogenic aerosols in the Indian monsoon using experiments in which observed trends in individual aerosol species are imposed. Sulphur dioxide (SD) emissions are shown to impact rainfall more strongly than black carbon (BC) aerosols, causing reduced rainfall especially over northern India. Significant perturbations due to BC are not noted until its emissions are scaled up in a sensitivity test, in which rainfall increases over northern India as a result of the Elevated Heat Pump mechanism, enhancing convection during the pre-monsoon and bringing forward the monsoon onset. Secondly, the impact of anthropogenic aerosols is compared to that of increasing greenhouse-gas concentrations and observed sea-surface temperature (SST) warming. The tropospheric temperature gradient driving the monsoon shows weakening when forced by either SD or imposed SST trends. However the observed SST trend is dominated by warming in the deep tropics; when the component of SST trend related to aerosol emissions is removed, further warming is found in the extratropical northern hemisphere that tends to offset monsoon weakening. This suggests caution is needed when using SST forcing as a proxy for greenhouse warming. Finally, aerosol emissions are decomposed into those from the Indian region and those elsewhere, in pairs of experiments with SD and BC. Both local and remote aerosol emissions are found to lead to rainfall changes over India; for SD, remote aerosols contribute around 75% of the rainfall decrease over India, while for BC the remote forcing is even more dominant.

  8. Detection of cw-related species in complex aerosol particles deposited on surfaces with an ion trap-based aerosol mass spectrometer

    SciTech Connect

    Harris, William A; Reilly, Pete; Whitten, William B

    2007-01-01

    A new type of aerosol mass spectrometer was developed by minimal modification of an existing commercial ion trap to analyze the semivolatile components of aerosols in real time. An aerodynamic lens-based inlet system created a well-collimated particle beam that impacted into the heated ionization volume of the commercial ion trap mass spectrometer. The semivolatile components of the aerosols were thermally vaporized and ionized by electron impact or chemical ionization in the source. The nascent ions were extracted and injected into the ion trap for mass analysis. The utility of this instrument was demonstrated by identifying semivolatile analytes in complex aerosols. This study is part of an ongoing effort to develop methods for identifying chemical species related to CW agent exposure. Our efforts focused on detection of CW-related species doped on omnipresent aerosols such as house dust particles vacuumed from various surfaces found in any office building. The doped aerosols were sampled directly into the inlet of our mass spectrometer from the vacuumed particle stream. The semivolatile analytes were deposited on house dust and identified by positive ion chemical ionization mass spectrometry up to 2.5 h after deposition. Our results suggest that the observed semivolatile species may have been chemisorbed on some of the particle surfaces in submonolayer concentrations and may remain hours after deposition. This research suggests that identification of trace CW agent-related species should be feasible by this technique.

  9. Modeling of photolysis rates over Europe: impact on chemical gaseous species and aerosols

    NASA Astrophysics Data System (ADS)

    Real, E.; Sartelet, K.

    2011-02-01

    This paper evaluates the impact of photolysis rate calculation on simulated European air composition and air quality. In particular, the impact of the cloud parametrisation and the impact of aerosols on photolysis rates are analysed. Photolysis rates are simulated using the Fast-JX photolysis scheme and gas and aerosol concentrations over Europe are simulated with the regional chemistry-transport model Polair3D of the Polyphemus platform. The photolysis scheme is first used to update the clear-sky tabulation of photolysis rates used in the previous Polair3D version. Important differences in photolysis rates are simulated, mainly due to updated cross-sections and quantum yields in the Fast-JX scheme. In the previous Polair3D version, clouds were taken into account by multiplying the clear-sky photolysis rates by a correction factor. In the new version, clouds are taken into account more accurately by simulating them directly in the photolysis scheme. Differences in photolysis rates inside clouds can be large but outside clouds, and especially at the ground, differences are small. To take into account the impact of aerosols on photolysis rates, Polair3D and Fast-JX are coupled. Photolysis rates are updated every hour. Large impact on photolysis rates is observed at the ground, decreasing with altitude. The aerosol specie that impact the most photolysis rates is dust especially in south Europe. Strong impact is also observed over anthropogenic emission regions (Paris, The Po and the Ruhr Valley) where mainly nitrate and sulphate reduce the incoming radiation. Differences in photolysis rates lead to changes in gas concentrations, with the largest impact simulated on OH and NO concentrations. At the ground, monthly mean concentrations of both species are reduced over Europe by around 10 to 14% and their tropospheric burden by around 10%. The decrease in OH leads to an increase of the life-time of several species such as VOC. NO2 concentrations are not strongly impacted

  10. Aerosol-halogen interaction: Change of physico-chemical properties of SOA by naturally released halogen species

    NASA Astrophysics Data System (ADS)

    Ofner, J.; Balzer, N.; Buxmann, J.; Grothe, H.; Krüger, H.; Platt, U.; Schmitt-Kopplin, P.; Zetzsch, C.

    2011-12-01

    Reactive halogen species are released by various sources like photo-activated sea-salt aerosol or salt pans and salt lakes. These heterogeneous release mechanisms have been overlooked so far, although their potential of interaction with organic aerosols like Secondary Organic Aerosol (SOA), Biomass Burning Organic Aerosol (BBOA) or Atmospheric Humic LIke Substances (HULIS) is completely unknown. Such reactions can constitute sources of gaseous organo-halogen compounds or halogenated organic particles in the atmospheric boundary layer. To study the interaction of organic aerosols with reactive halogen species (RHS), SOA was produced from α-pinene, catechol and guaiacol using an aerosol smog-chamber. The model SOAs were characterized in detail using a variety of physico-chemical methods (Ofner et al., 2011). Those aerosols were exposed to molecular halogens in the presence of UV/VIS irradiation and to halogens, released from simulated natural halogen sources like salt pans, in order to study the complex aerosol-halogen interaction. The heterogeneous reaction of RHS with those model aerosols leads to different gaseous species like CO2, CO and small reactive/toxic molecules like phosgene (COCl2). Hydrogen containing groups on the aerosol particles are destroyed to form HCl or HBr, and a significant formation of C-Br bonds could be verified in the particle phase. Carbonyl containing functional groups of the aerosol are strongly affected by the halogenation process. While changes of functional groups and gaseous species were visible using FTIR spectroscopy, optical properties were studied using Diffuse Reflectance UV/VIS spectroscopy. Overall, the optical properties of the processed organic aerosols are significantly changed. While chlorine causes a "bleaching" of the aerosol particles, bromine shifts the maximum of UV/VIS absorption to the red end of the UV/VIS spectrum. Further physico-chemical changes were recognized according to the aerosol size-distributions or the

  11. Multiple Types of Light Absorbing Carbon Aerosol in East Asian Outflow: Variatons in Morphology and Internal Structure as Characterized by Transmission Electron Microscopy

    NASA Astrophysics Data System (ADS)

    Anderson, J. R.; Alexander, D. T.; Crozier, P. A.

    2010-12-01

    The importance of light absorbing carbon (LAC) aerosols to climate forcing is well established, but such aerosols are typically treated in climate models as uniform in optical properties. When examined by electron microscopy, however, LAC aerosols from regions with significant anthropogenic pollution show a wide variety of morphologies and internal structures. Electron energy loss spectral analysis to date on brown carbon and black carbon, albeit limited, suggests a linkage between internal structure and fundamental optical properties. Some of these LAC varieties can be easily defined as distinct “types” and other varieties show a continuum of variation within which general “types” can be defined. The data discussed here are from a research flight of the NCAR C-130 aircraft flown in April 2001 above the Yellow Sea during the ACE-Asia project. Perhaps the most common LAC type is “soot”, branched and chainlike aggregates of carbonaceous spherules. The spherule size in East Asian soot particles is 20-60 nm in many cases, but soot with large spherules (100 nm or larger) are also present. Spherule size is a “source effect” and not something altered during transport and aging. Some laboratory studies have suggested that as soot ages, the aggregates become more compact, but in these aerosols both compact and open soot particles coexist and compact soot is known to be the initial LAC product under some combustion conditions. In cases where the spherule size of the compact soot is different from that of open-structured soot, clearly the compact soot is not an aged form of the latter. Variability of ordering of the graphene sheets that make up the spherules is also a source effect. The more ordered soot particles consist of graphene sheets that curve concentrically, onion-like, around the spherule center, probably indicative of a high degree of carbonization that accompanies high temperature combustion. There is a range of ordering from highly ordered down to

  12. Evidence of a Weakly Absorbing Intermediate Mode of Aerosols in AERONET Data from Saharan and Sahelian Sites

    NASA Technical Reports Server (NTRS)

    Gianelli, Scott M.; Lacis, Andrew A.; Carlson, Barbara E.; Hameed, Sultan

    2013-01-01

    Accurate retrievals of aerosol size distribution are necessary to estimate aerosols' impact on climate and human health. The inversions of the Aerosol Robotic Network (AERONET) usually retrieve bimodal distributions. However, when the inversion is applied to Saharan and Sahelian dust, an additional mode of intermediate size between the coarse and fine modes is sometimes seen. This mode explains peculiarities in the behavior of the Angstrom exponent, along with the fine mode fraction retrieved using the spectral deconvolution algorithm, observed in a March 2006 dust storm. For this study, 15 AERONET sites in northern Africa and on the Atlantic are examined to determine the frequency and properties of the intermediate mode. The mode is observed most frequently at Ilorin in Nigeria. It is also observed at Capo Verde and multiple sites located within the Sahel but much less frequently at sites in the northern Sahara and the Canary Islands. The presence of the intermediate mode coincides with increases in Angstrom exponent, fine mode fraction, single-scattering albedo, and to a lesser extent percent sphericity. The Angstrom exponent decreases with increasing optical depth at most sites when the intermediate mode is present, but the fine mode fraction does not. Single-scattering albedo does not steadily decrease with fine mode fraction when the intermediate mode is present, as it does in typical mixtures of dust and biomass-burning aerosols. Continued investigation is needed to further define the intermediate mode's properties, determine why it differs from most Saharan dust, and identify its climate and health effects.

  13. Soluble species in the Arctic summer troposphere - Acidic gases, aerosols, and precipitation

    NASA Technical Reports Server (NTRS)

    Talbot, R. W.; Vijgen, A. S.; Harriss, R. C.

    1992-01-01

    The large-scale spatial distribution from 0.15-to 6 km altitude in the North American Arctic troposphere of several soluble acidic gases and major aerosol species during the summertime is reported. The distribution is found to be compositionally consistent on a large spatial scale. The summertime troposphere is an acidic environment, with HCOOH and CH3COOH the principal acidic gases while acidic sulfate aerosols dominate the particulate phase. There appears to be a surface source of NH3 over the pack ice which may originate from decay of dead marine organisms on the ice surface, evolution from surface ocean waters in open ice leads, or release from rotting sea ice. At low altitude over the pack ice this NH34 appears to partially neutralize aerosol acidity. Over sub-Arctic tundra in southeastern Alaska, inputs of marine biogenic sulfur from the Bering Sea appear to be an important source of boundary layer aerosol SO4(2-). The rainwater acidity over the tundra is typical of remote regions.

  14. Soluble species in the Arctic summer troposphere - acidic gases, aerosols, and precipitation

    SciTech Connect

    Talbot, R.W.; Vijgen, A.S.; Harriss, R.C. Old Dominion Univ., Norfolk, VA )

    1992-10-01

    The large-scale spatial distribution from 0.15-to 6 km altitude in the North American Arctic troposphere of several soluble acidic gases and major aerosol species during the summertime is reported. The distribution is found to be compositionally consistent on a large spatial scale. The summertime troposphere is an acidic environment, with HCOOH and CH3COOH the principal acidic gases while acidic sulfate aerosols dominate the particulate phase. There appears to be a surface source of NH3 over the pack ice which may originate from decay of dead marine organisms on the ice surface, evolution from surface ocean waters in open ice leads, or release from rotting sea ice. At low altitude over the pack ice this NH34 appears to partially neutralize aerosol acidity. Over sub-Arctic tundra in southeastern Alaska, inputs of marine biogenic sulfur from the Bering Sea appear to be an important source of boundary layer aerosol SO4(2-). The rainwater acidity over the tundra is typical of remote regions. 61 refs.

  15. Experiment to Characterize Aircraft Volatile Aerosol and Trace-Species Emissions (EXCAVATE)

    NASA Technical Reports Server (NTRS)

    Anderson, B. E.; Branham, H.-S.; Hudgins, C. H.; Plant, J. V.; Ballenthin, J. O.; Miller, T. M.; Viggiano, A. A.; Blake, D. R.; Boudries, H.; Canagaratna, M.

    2005-01-01

    The Experiment to Characterize Aircraft Volatile and Trace Species Emissions (EXCAVATE) was conducted at Langley Research Center (LaRC) in January 2002 and focused upon assaying the production of aerosols and aerosol precursors by a modern commercial aircraft, the Langley B757, during ground-based operation. Remaining uncertainty in the postcombustion fate of jet fuel sulfur contaminants, the need for data to test new theories of particle formation and growth within engine exhaust plumes, and the need for observations to develop air quality models for predicting pollution levels in airport terminal areas were the primary factors motivating the experiment. NASA's Atmospheric Effects of Aviation Project (AEAP) and the Ultra Effect Engine Technology (UEET) Program sponsored the experiment which had the specific objectives of determining ion densities; the fraction of fuel S converted from S(IV) to S(VI); the concentration and speciation of volatile aerosols and black carbon; and gas-phase concentrations of long-chain hydrocarbon and PAH species, all as functions of engine power, fuel composition, and plume age.

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

    NASA Astrophysics Data System (ADS)

    Randles, C. A.; Ramaswamy, V.

    2007-12-01

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

  17. Soluble species in the Arctic summer troposphere: Acidic gases, aerosols, and precipitation

    NASA Astrophysics Data System (ADS)

    Talbot, R. W.; Vijgen, A. S.; Harriss, R. C.

    1992-10-01

    We report here the distribution of selected acidic gases and aerosol species in the North American Arctic and sub-Arctic summer troposphere. The summertime troposphere is an acidic environment, with HCOOH and CH3COOH the principal acidic gases and acidic sulfate aerosols dominating the particulate phase. Our data show that the acidic gas and aerosol composition is uniform on a large spatial scale. There appears to be a surface source of NH4+ over the Arctic Ocean pack ice which may reflect release of NH3 from decay of dead marine organisms on the ice surface near ice leads, release from rotting sea ice, or an upward flux from surface ocean waters in open ice leads. This NH3 appears to partially neutralize aerosol acidity in the boundary layer. Over sub-Arctic tundra in southwestern Alaska inputs of marine biogenic sulfur from the nearby Bering Sea appear to be an important source of boundary layer aerosol SO42-. While there were only minor effects on aerosol chemistry over the tundra from sea salt, the rainwater chemistry showed influence from marine aerosols which were apparently incorporated into air masses during frontal passages moving inland from the Bering Sea. The rainwater acidity over the tundra (pH 4.69) is typical of remote regions. The principal acidity components are H2SO4 and carboxylic acids, especially HCOOH. The carboxylic acids appear to have a strong continental biogenic source, but hydrocarbons of marine origin and emissions from forest fires may also be important. The wet deposition fluxes of NO3--N and SO42--S over sub-Arctic tundra during July-August 1988 were 2.1 and 2.4 mmol m-2 yr-1. Wet deposition of NO3- was nearly 3 times higher than the average NOy deposition flux, which is believed to represent primarily dry deposition of HNO3 (Bakwin et al., this issue). Our measurements indicate that the mid-troposphere in the Arctic is generally contaminated with low levels of anthropogenic pollutants even in summer when direct atmospheric coupling

  18. Measurements of trace gas species and aerosols at three Siberian stations

    NASA Astrophysics Data System (ADS)

    Arshinov, Mikhail Yu.; Belan, Boris D.; Davydov, Denis K.; Kozlov, Artem V.; Ivlev, Georgii A.; Pestunov, Dmitrii A.; Tolmachev, Gennadii N.; Fofonov, Alexander V.

    2014-05-01

    Siberia is of great importance to understand the climate change due to it covers about 10% of Earth's land surface and it has the largest area to be studied under the Pan-Eurasian Experiment (PEEX). In the overview done by Kulmala et al. (2011) authors arrived at a conclusion that continuous and comprehensive measurements of GHGs and aerosols over Siberia are still lacking. Understanding the importance of this problem, in recent years the Institute of Atmospheric Optics SB RAS established several monitoring stations for continuous measurements of aerosol and trace gas species to fill up this gap. In this paper we present some results of continuous measurements of trace gas species and aerosols carried out at three stations located in West Siberia. The first one is a so-called TOR-station located in the scientific campus of Tomsk (56° 28'41"N, 85° 03'15"E), the second one is the Base Experimental Complex (BEC, 56° 28'49"N, 85° 06'08"E) - in the eastern suburbs of Tomsk, and the third one is Fonovaya Observatory (56° 25'07"N, 84° 04'27"E) - in a rural area 60 km west of Tomsk. All equipment of the stations is fully automated and can be monitored via Internet. Gas analyzers are hourly calibrated against standard gas mixtures, micro-flux gas sources, or gas generators, depending on the instrument type and the gas to be detected. Aerosol measurements carried out continuously from March 2010 enabled a frequency and seasonal dependency of the new particle formation (NPF) events to be revealed. NPF events in Siberia are more often observed during spring (from March to May) and early autumn (secondary frequency peak in September). On average, NPF evens took place on 23-28 % of all days. This work was funded by Presidium of RAS (Program No. 4), Brunch of Geology, Geophysics and Mining Sciences of RAS (Program No. 5), Interdisciplinary integration projects of Siberian Branch of RAS (No. 35, No. 70, No. 131), Russian Foundation for Basic Research (grants No 14

  19. Water-Soluble Organic Species in Biomass Burning Aerosols in Southern Africa: Their Chemical Identification and Spatial Distribution

    NASA Astrophysics Data System (ADS)

    Gao, S.; Hegg, D. A.; Hobbs, P. V.; Kirchstetter, T. W.; Magi, B.

    2001-12-01

    During the SAFARI-2000 field campaign, 14 aerosol samples were collected from an aircraft in plumes from biomass fires (under both flaming and smoldering conditions), at various distances from the fire source. Also collected were 36 aerosol samples in haze layers ranging from the surface to 16,000 feet, some of which could be associated with specific fires. The samples were collected on teflon membrane filters (lower size limit of about 30nm in diameter) which were analyzed for total aerosol mass loading and chemical composition using several analytical techniques. Particular effort was made to speciate the water-soluble portion of the aerosol organics. Seven organic acids and seven carbohydrate species (and their possible stereoisomers) were identified and quantified, along with three inorganic anions and five inorganic cations. The identified organic species accounted for up to 32% of the total aerosol mass; compared with concurrent total carbon and organic carbon measurements, the identified organics constituted at least 5% to 30% of the mass of the total aerosol organics. A number of conspicuous spatial distribution patterns were observed for these species. For instance, using K+ to correct for dilution, it was found that gluconate, oxalate, succinate, and glutarate, along with sulfate and nitrate, all increased significantly in mass concentration from the fire source going downwind. This suggests secondary formation of these species during aerosol aging. On the other hand, formate and acetate showed decreasing trends downwind, probably due to the loss of these volatile species to the gas phase. Another striking pattern is that anhydrosugars (e.g. levoglucosan) had the highest aerosol mass fraction near smoldering fires but a very low fraction in the haze layers, whereas, dicarboxylic acids showed an almost opposite trend. This implies possible chemical reaction processes converting intermediate organic products, such as levoglucosan, to smaller products like

  20. Efficacy and immunogenicity of single-dose AdVAV intranasal anthrax vaccine compared to anthrax vaccine absorbed in an aerosolized spore rabbit challenge model.

    PubMed

    Krishnan, Vyjayanthi; Andersen, Bo H; Shoemaker, Christine; Sivko, Gloria S; Tordoff, Kevin P; Stark, Gregory V; Zhang, Jianfeng; Feng, Tsungwei; Duchars, Matthew; Roberts, M Scot

    2015-04-01

    AdVAV is a replication-deficient adenovirus type 5-vectored vaccine expressing the 83-kDa protective antigen (PA83) from Bacillus anthracis that is being developed for the prevention of disease caused by inhalation of aerosolized B. anthracis spores. A noninferiority study comparing the efficacy of AdVAV to the currently licensed Anthrax Vaccine Absorbed (AVA; BioThrax) was performed in New Zealand White rabbits using postchallenge survival as the study endpoint (20% noninferiority margin for survival). Three groups of 32 rabbits were vaccinated with a single intranasal dose of AdVAV (7.5 × 10(7), 1.5 × 10(9), or 3.5 × 10(10) viral particles). Three additional groups of 32 animals received two doses of either intranasal AdVAV (3.5 × 10(10) viral particles) or intramuscular AVA (diluted 1:16 or 1:64) 28 days apart. The placebo group of 16 rabbits received a single intranasal dose of AdVAV formulation buffer. All animals were challenged via the inhalation route with a targeted dose of 200 times the 50% lethal dose (LD50) of aerosolized B. anthracis Ames spores 70 days after the initial vaccination and were followed for 3 weeks. PA83 immunogenicity was evaluated by validated toxin neutralizing antibody and serum anti-PA83 IgG enzyme-linked immunosorbent assays (ELISAs). All animals in the placebo cohort died from the challenge. Three of the four AdVAV dose cohorts tested, including two single-dose cohorts, achieved statistical noninferiority relative to the AVA comparator group, with survival rates between 97% and 100%. Vaccination with AdVAV also produced antibody titers with earlier onset and greater persistence than vaccination with AVA.

  1. Determination of the passing efficiency for aerosol chemical species through a typical aircraft-mounted, diffuser-type aerosol inlet system

    NASA Astrophysics Data System (ADS)

    Sheridan, Patrick J.; Norton, Richard B.

    1998-04-01

    To assess the particle transmission efficiency of a conventional aircraft-mounted, diffuser-type inlet (CI), a new design inlet containing an internal filter basket assembly (aerosol filter inlet, or AFI) was constructed. All interior surfaces of the AFI were covered with filter material, and air was actively pulled through these filter walls during aerosol sampling. The AFI was demonstrated in the laboratory to trap nearly all particles entering its nozzle orifice, so it was considered usable as a baseline to judge the performance of other inlets. Wind tunnel studies were conducted at three different wind velocities that approximated typical research aircraft speeds. As wind velocity increased, particle transmission through the CI relative to the AFI decreased, as evidenced by chemical analysis of the filter deposits. Aircraft studies of the two inlets showed that particle transmission varied significantly with the measured species. Typical coarse-particle species such as Ca++, Mg++, Na+ and K+ showed 50-90% mass losses through a conventional diffuser-type inlet/curved intake tube system. Predominantly fine particle species such as SO4= and NH4+ passed the CI system with much higher efficiencies, with aerosol mass losses of 0-26% for most flights. Since the AFI traps nearly all particles aspirated into its nozzle orifice, these values indicate that on average, 80-90% of the SO4= and NH4+ aerosol mass passes through the CI and curved intake tube during airborne sampling. This finding suggests that the capability to sample fine (i.e., submicrometer) aerosols from aircraft is perhaps not as bad as has been previously reported, given that adequate attention is paid to inlet design, location, and orientation issues.

  2. Mass absorption efficiency of light absorbing organic aerosols from source region of paddy-residue burning emissions in the Indo-Gangetic Plain

    NASA Astrophysics Data System (ADS)

    Srinivas, B.; Rastogi, N.; Sarin, M. M.; Singh, A.; Singh, D.

    2016-01-01

    The mass absorption efficiency (MAE) of light absorbing water-soluble organics, representing a significant fraction of brown carbon (BrC), has been studied in fine mode aerosols (PM2.5) from a source region (Patiala: 30.2 °N, 76.3 °E) of biomass burning emissions (BBEs) in the Indo-Gangetic Plain (IGP). The mass absorption coefficient of BrC at 365 nm (babs-365), assessed from absorption spectra of aqueous extracts, exhibits significant linear relationship with water-soluble organic carbon (WSOC) for day (R2 = 0.37) and night time (R2 = 0.77) samples; and slope of regression lines provides a measure of MAE of BrC (daytime: ˜0.75 m2 g-1 and night time: 1.13 m2 g-1). A close similarity in the temporal variability of babs-365 (for BrC) and K+ in all samples suggests their common source from BBEs. The babs-365 of BrC follows a power law (babs-λ ≈ λ-α; where α = angstrom exponent) and averages around 5.2 ± 2.0 M m-1 (where M = 10-6). A significant decrease in the MAE of BrC from the source region (this study) to the downwind oceanic region (over Bay of Bengal, Srinivas and Sarin, 2013) could be attributed to relative increase in the contribution of non-absorbing WSOC and/or photo-bleaching of BrC during long-range atmospheric transport. The atmospheric radiative forcing due to BrC over the study site accounts for ˜40% of that from elemental carbon (EC).

  3. Measurement of acidic aerosol species in eastern Europe: implications for air pollution epidemiology.

    PubMed Central

    Brauer, M; Dumyahn, T S; Spengler, J D; Gutschmidt, K; Heinrich, J; Wichmann, H E

    1995-01-01

    A large number of studies have indicated associations between particulate air pollution and adverse health outcomes. Wintertime air pollution in particular has been associated with increased mortality. Identification of causal constituents of inhalable particulate matter has been elusive, although one candidate has been the acidity of the aerosol. Here we report measurements of acidic aerosol species made for approximately 1.5 years in Erfurt, Germany, and Sokolov, Czech Republic. In both locations, the burning of high-sulfur coal is the primary source of ambient air pollution. Twenty-four-hour average measurements were made for PM10, [particulate matter with an aerodynamic diameter (da) < or = 10 microns], as well as fine particle (da < 2.5 microns) H+ and SO4(2-) for the entire study. Additionally, separate day and night measurements of fine particle H+, SO4(2-), NO3-, and NH4+ and the gases, SO2, HNO3, HONO, and NH3 were collected with an annular denuder/filter pack system over a 7-month (late winter-summer) period with additional measurements during pollution episodes the following winter. At both sites, 24-hr SO2 (mean concentrations of 52 micrograms/m3, with peak levels of > 585 micrograms/m3) and PM10 (mean concentration 60 micrograms m3) concentrations were quite high. However, aerosol SO4(2-) concentrations (mean concentration of approximately 10 micrograms/m3) were not as great as expected given the high SO2 concentrations, and acidity was very low (mean concentration of < 1 microgram/m3, with peak levels of only 7 micrograms/m3). Low acidity is likely to be the result of NH3 neutralization and slow conversion of SO2 to SO4(2-).(ABSTRACT TRUNCATED AT 250 WORDS) PMID:7656878

  4. Background error covariance with balance constraints for aerosol species and applications in variational data assimilation

    NASA Astrophysics Data System (ADS)

    Zang, Zengliang; Hao, Zilong; Li, Yi; Pan, Xiaobin; You, Wei; Li, Zhijin; Chen, Dan

    2016-08-01

    Balance constraints are important for background error covariance (BEC) in data assimilation to spread information between different variables and produce balance analysis fields. Using statistical regression, we develop a balance constraint for the BEC of aerosol variables and apply it to a three-dimensional variational data assimilation system in the WRF/Chem model; 1-month forecasts from the WRF/Chem model are employed for BEC statistics. The cross-correlations between the different species are generally high. The largest correlation occurs between elemental carbon and organic carbon with as large as 0.9. After using the balance constraints, the correlations between the unbalanced variables reduce to less than 0.2. A set of data assimilation and forecasting experiments is performed. In these experiments, surface PM2.5 concentrations and speciated concentrations along aircraft flight tracks are assimilated. The analysis increments with the balance constraints show spatial distributions more complex than those without the balance constraints, which is a consequence of the spreading of observation information across variables due to the balance constraints. The forecast skills with the balance constraints show substantial and durable improvements from the 2nd hour to the 16th hour compared with the forecast skills without the balance constraints. The results suggest that the developed balance constraints are important for the aerosol assimilation and forecasting.

  5. Multiple-wavelength spectroscopic quantitation of light-absorbing species in scattering media

    DOEpatents

    Nathel, Howard; Cartland, Harry E.; Colston, Jr., Billy W.; Everett, Matthew J.; Roe, Jeffery N.

    2000-01-01

    An oxygen concentration measurement system for blood hemoglobin comprises a multiple-wavelength low-coherence optical light source that is coupled by single mode fibers through a splitter and combiner and focused on both a target tissue sample and a reference mirror. Reflections from both the reference mirror and from the depths of the target tissue sample are carried back and mixed to produce interference fringes in the splitter and combiner. The reference mirror is set such that the distance traversed in the reference path is the same as the distance traversed into and back from the target tissue sample at some depth in the sample that will provide light attenuation information that is dependent on the oxygen in blood hemoglobin in the target tissue sample. Two wavelengths of light are used to obtain concentrations. The method can be used to measure total hemoglobin concentration [Hb.sub.deoxy +Hb.sub.oxy ] or total blood volume in tissue and in conjunction with oxygen saturation measurements from pulse oximetry can be used to absolutely quantify oxyhemoglobin [HbO.sub.2 ] in tissue. The apparatus and method provide a general means for absolute quantitation of an absorber dispersed in a highly scattering medium.

  6. Evaluation of multistep derivatization methods for identification and quantification of oxygenated species in organic aerosol.

    PubMed

    Flores, Rosa M; Doskey, Paul V

    2015-10-30

    Two, 3-step methods for derivatizing mono- and multi-functional species with carbonyl (CO), carboxylic acid (-COOH), and alcohol (-OH) moieties were compared and optimized. In Method 1, the CO, -COOH, and -OH moieties were converted (1) to methyloximes (R-CN-OCH3) with O-methylhydroxylamine hydrochloride (MHA), (2) to methyl esters (OC-R-OCH3) with (trimethylsilyl)diazomethane in methanol (TMSD/MeOH), and (3) to trimethylsilyl ethers [R-OSi(CH3)3] with N,O-bis(trimethylsilyl)-trifluoroacetamide (BSTFA) containing 1% trimethylchlorosilane (TMCS), respectively. Steps 1 and 3 of both methods were identical; however, in Step 2 of Method 2, -COOH moieties were derivatized with 10% (v/v) boron trifluoride (BF3) in MeOH or n-butanol (n-BuOH). The BF3/MeOH and BF3/n-BuOH were ineffective at converting species with more than 2-OH moieties. Average standard deviations for derivatization of 36 model compounds by the 3-step methods using TMSD/MeOH and BF3/(MeOH) were 7.4 and 14.8%, respectively. Average derivatization efficiencies for Methods 1 and 2 were 88.0 and 114%, respectively. Despite the lower average derivatization efficiency of Method 1, distinct advantages included a greater certainty of derivatization yield for the entire suite of mono- and multi-functional species and fewer processing steps for sequential derivatization. Detection limits for Method 1 using GC×GC-ToF-MS were 0.3-54pgm(-3). Approximately 100 oxygenated organic species were identified and quantified in aerosol filtered from 39m(3) of air in an urban location. Levels of species were 0.013-17ngm(-3) and were nearly all above the Method 1 limit of detection.

  7. Halogen-induced organic aerosol (XOA) formation and decarboxylation of carboxylic acids by reactive halogen species - a time-resolved aerosol flow-reactor study

    NASA Astrophysics Data System (ADS)

    Ofner, Johannes; Zetzsch, Cornelius

    2013-04-01

    Reactive halogen species (RHS) are released to the atmosphere from various sources like photo-activated sea-salt aerosol and salt lakes. Recent studies (Cai et al., 2006 and 2008, Ofner et al., 2012) indicate that RHS are able to interact with SOA precursors similarly to common atmospheric oxidizing gases like OH radicals and ozone. The reaction of RHS with SOA precursors like terpenes forms so-called halogen-induced organic aerosol (XOA). On the other hand, RHS are also able to change the composition of functional groups, e.g. to initiate the decarboxylation of carboxylic acids (Ofner et al., 2012). The present study uses a 50 cm aerosol flow-reactor, equipped with a solar simulator to investigate the time-resolved evolution and transformation of vibrational features in the mid-infrared region. The aerosol flow-reactor is coupled to a home-made multi-reflection cell (Ofner et al., 2010), integrated into a Bruker IFS 113v FTIR spectrometer. The reactor is operated with an inlet feed (organic compound) and a surrounding feed (reactive halogen species). The moveable inlet of the flow reactor allows us to vary reaction times between a few seconds and up to about 3 minutes. Saturated vapours of different SOA precursors and carboxylic acids were fed into the flow reactor using the moveable inlet. The surrounding feed inside the flow reactor was a mixture of zero air with molecular chlorine as the precursor for the formation of reactive halogen species. Using this setup, the formation of halogen-induced organic aerosol could be monitored with a high time resolution using FTIR spectroscopy. XOA formation is characterized by hydrogen-atom abstraction, carbon-chlorine bond formation and later, even formation of carboxylic acids. Several changes of the entire structure of the organic precursor, caused by the reaction of RHS, are visible. While XOA formation is a very fast process, the decarboxylation of carboxylic acids, induced by RHS is rather slow. However, XOA formation

  8. High-resolution modeling of the influences of absorbing aerosols on rainfall over northern India and the Himalaya foothills during boreal summer

    NASA Astrophysics Data System (ADS)

    Kim, K.; Lau, W. K.; Tao, W.; Shi, J. J.; Tan, Q.; Chin, M.; Matsui, T.; Kemp, E. M.; Peters-Lidard, C. D.

    2012-12-01

    High elevation and steep topography of Tibetan Plateau and the Himalayas foothills regions are important components of the South Asian summer monsoon system. Strong orographic forcing combined with abundant moisture from the Arabian Sea and the Bay of Bengal and aerosols stacked up against the southern slope of the Tibetan Plateau produce complex physical and dynamical effects on monsoon rainfall and circulation. In this work, we use the NASA Unified Weather Research and Forecasting (Nu-WRF) model to study the effect of aerosol radiative forcing on the short-term predictability (1-7 days) of the South Asian monsoon rainfall system. Two sets of 7-day forecasting experiments were conducted with and without aerosol radiative forcing. Each set consists of 34 7-day forcasts with initial conditions from daily reanalysis and GEOS-5 aerosol distribution (only for aerosol run) from June 11- July 14, 2008. Nu-WRF, without aerosol forcing captures the horizontal distribution of 7-day mean precipitation reasonably well, but it tends to over-estimates rainfall over the central India. The biases are especially larger in the upwind side of the western Ghats and northeast India and Bangladesh. Preliminary results show that inclusion of aerosol radiative forcing and interaction with dynamics reduces rainfall over the Indo-Gangetic plain where aerosol loadinng is high, but enhances rainfall downstream of the prevailing monsoon flow in the southern slope of Tibetan Plateau, especially over the northeast India and foothills regions, consistent with the EHP hypothesis. Effect of aerosol radiative forcing is small during the first two days of forecasts. Rainfall anomalies generated by atmospheric feedback induced by aerosol radiative forcing becomes statistically significant and large enough to be separable from growing model biases after three days of simulation. The results indicate the inclusion of aerosol radiative forcing may improve short-term (4-7 day) forecasting skill in

  9. Probing Coagulation Behavior of Individual Aluminum Species for Removing Corresponding Disinfection Byproduct Precursors: The Role of Specific Ultraviolet Absorbance

    PubMed Central

    Zhao, He; Hu, Chengzhi; Zhang, Di; Liu, Huijuan; Qu, Jiuhui

    2016-01-01

    Coagulation behavior of aluminum chloride and polyaluminum chloride (PACl) for removing corresponding disinfection byproduct (DBP) precursors was discussed in this paper. CHCl3, bromine trihalomethanes (THM-Br), dichloroacetic acid (DCAA) and trichloroacetic acid (TCAA) formation potential yields were correlated with specific ultraviolet absorbance (SUVA) values in different molecular weight (MW) fractions of humic substances (HS), respectively. Correlation analyses and principal component analysis were performed to examine the relationships between SUVA and different DBP precursors. To acquire more structural characters of DBP precursors and aluminum speciation, freeze-dried precipitates were analyzed by fourier transform infrared (FTIR) and C 1s, Al 2p X-ray photoelectron spectroscopy (XPS). The results indicated that TCAA precursors (no MW limits), DCAA and CHCl3 precursors in low MW fractions (MW<30 kDa) had a relatively good relations with SUVA values. These DBP precursors were coagulated more easily by in situ Al13 of AlCl3 at pH 5.0. Due to relatively low aromatic content and more aliphatic structures, THM-Br precursors (no MW limits) and CHCl3 precursors in high MW fractions (MW>30 kDa) were preferentially removed by PACl coagulation with preformed Al13 species at pH 5.0. Additionally, for DCAA precursors in high MW fractions (MW>30 kDa) with relatively low aromatic content and more carboxylic structures, the greatest removal occurred at pH 6.0 through PACl coagulation with aggregated Al13 species. PMID:26824243

  10. Probing Coagulation Behavior of Individual Aluminum Species for Removing Corresponding Disinfection Byproduct Precursors: The Role of Specific Ultraviolet Absorbance.

    PubMed

    Zhao, He; Hu, Chengzhi; Zhang, Di; Liu, Huijuan; Qu, Jiuhui

    2016-01-01

    Coagulation behavior of aluminum chloride and polyaluminum chloride (PACl) for removing corresponding disinfection byproduct (DBP) precursors was discussed in this paper. CHCl3, bromine trihalomethanes (THM-Br), dichloroacetic acid (DCAA) and trichloroacetic acid (TCAA) formation potential yields were correlated with specific ultraviolet absorbance (SUVA) values in different molecular weight (MW) fractions of humic substances (HS), respectively. Correlation analyses and principal component analysis were performed to examine the relationships between SUVA and different DBP precursors. To acquire more structural characters of DBP precursors and aluminum speciation, freeze-dried precipitates were analyzed by fourier transform infrared (FTIR) and C 1s, Al 2p X-ray photoelectron spectroscopy (XPS). The results indicated that TCAA precursors (no MW limits), DCAA and CHCl3 precursors in low MW fractions (MW<30 kDa) had a relatively good relations with SUVA values. These DBP precursors were coagulated more easily by in situ Al13 of AlCl3 at pH 5.0. Due to relatively low aromatic content and more aliphatic structures, THM-Br precursors (no MW limits) and CHCl3 precursors in high MW fractions (MW>30 kDa) were preferentially removed by PACl coagulation with preformed Al13 species at pH 5.0. Additionally, for DCAA precursors in high MW fractions (MW>30 kDa) with relatively low aromatic content and more carboxylic structures, the greatest removal occurred at pH 6.0 through PACl coagulation with aggregated Al13 species.

  11. Organic aerosols associated with the generation of reactive oxygen species (ROS) by water-soluble PM2.5.

    PubMed

    Verma, Vishal; Fang, Ting; Xu, Lu; Peltier, Richard E; Russell, Armistead G; Ng, Nga Lee; Weber, Rodney J

    2015-04-07

    We compare the relative toxicity of various organic aerosol (OA) components identified by an aerosol mass spectrometer (AMS) based on their ability to generate reactive oxygen species (ROS). Ambient fine aerosols were collected from urban (three in Atlanta, GA and one in Birmingham, AL) and rural (Yorkville, GA and Centerville, AL) sites in the Southeastern United States. The ROS generating capability of the water-soluble fraction of the particles was measured by the dithiothreitol (DTT) assay. Water-soluble PM extracts were further separated into the hydrophobic and hydrophilic fractions using a C-18 column, and both fractions were analyzed for DTT activity and water-soluble metals. Organic aerosol composition was measured at selected sites using a high-resolution time-of-flight AMS. Positive matrix factorization of the AMS spectra resolved the organic aerosol into isoprene-derived OA (Isop_OA), hydrocarbon-like OA (HOA), less-oxidized oxygenated OA, (LO-OOA), more-oxidized OOA (MO-OOA), cooking OA (COA), and biomass burning OA (BBOA). The association of the DTT activity of water-soluble PM2.5 (WS_DTT) with these factors was investigated by linear regression techniques. BBOA and MO-OOA were most consistently linked with WS_DTT, with intrinsic water-soluble activities of 151 ± 20 and 36 ± 22 pmol/min/μg, respectively. Although less toxic, MO-OOA was most widespread, contributing to WS_DTT activity at all sites and during all seasons. WS_DTT activity was least associated with biogenic secondary organic aerosol. The OA components contributing to WS_DTT were humic-like substances (HULIS), which are abundantly emitted in biomass burning (BBOA) and include highly oxidized OA from multiple sources (MO-OOA). Overall, OA contributed approximately 60% to the WS_DTT activity, with the remaining probably from water-soluble metals, which were mostly associated with the hydrophilic WS_DTT fraction.

  12. Quantification of environmentally persistent free radicals and reactive oxygen species in atmospheric aerosol particles

    NASA Astrophysics Data System (ADS)

    Arangio, Andrea M.; Tong, Haijie; Socorro, Joanna; Pöschl, Ulrich; Shiraiwa, Manabu

    2016-10-01

    Fine particulate matter plays a central role in the adverse health effects of air pollution. Inhalation and deposition of aerosol particles in the respiratory tract can lead to the release of reactive oxygen species (ROS), which may cause oxidative stress. In this study, we have detected and quantified a wide range of particle-associated radicals using electron paramagnetic resonance (EPR) spectroscopy. Ambient particle samples were collected using a cascade impactor at a semi-urban site in central Europe, Mainz, Germany, in May-June 2015. Concentrations of environmentally persistent free radicals (EPFR), most likely semiquinone radicals, were found to be in the range of (1-7) × 1011 spins µg-1 for particles in the accumulation mode, whereas coarse particles with a diameter larger than 1 µm did not contain substantial amounts of EPFR. Using a spin trapping technique followed by deconvolution of EPR spectra, we have also characterized and quantified ROS, including OH, superoxide (O2-) and carbon- and oxygen-centered organic radicals, which were formed upon extraction of the particle samples in water. Total ROS amounts of (0.1-3) × 1011 spins µg-1 were released by submicron particle samples and the relative contributions of OH, O2-, C-centered and O-centered organic radicals were ˜ 11-31, ˜ 2-8, ˜ 41-72 and ˜ 0-25 %, respectively, depending on particle sizes. OH was the dominant species for coarse particles. Based on comparisons of the EPR spectra of ambient particulate matter with those of mixtures of organic hydroperoxides, quinones and iron ions followed by chemical analysis using liquid chromatography mass spectrometry (LC-MS), we suggest that the particle-associated ROS were formed by decomposition of organic hydroperoxides interacting with transition metal ions and quinones contained in atmospheric humic-like substances (HULIS).

  13. Efficacy of RNA interference knockdown using aerosolized short interfering RNAs bound to nanoparticles in three diverse aphid species.

    PubMed

    Thairu, M W; Skidmore, I H; Bansal, R; Nováková, E; Hansen, T E; Li-Byarlay, H; Wickline, S A; Hansen, A K

    2017-03-17

    RNA interference (RNAi) has emerged as a promising method for validating gene function; however, its utility in nonmodel insects has proven problematic, with delivery methods being one of the main obstacles. This study investigates a novel method of RNAi delivery in aphids, the aerosolization of short interfering RNA (siRNA)-nanoparticle complexes. By using nanoparticles as a siRNA carrier, the likelihood of cellular uptake is increased, when compared to methods previously used in insects. To determine the efficacy of this RNAi delivery system, siRNAs were aerosolized with and without nanoparticles in three aphid species: Acyrthosiphon pisum, Aphis glycines and Schizaphis graminum. The genes targeted for knockdown were carotene dehydrogenase (tor), which is important for pigmentation in Ac. pisum, and branched chain-amino acid transaminase (bcat), which is essential in the metabolism of branched-chain amino acids in all three aphid species. Overall, we observed modest gene knockdown of tor in Ac. pisum and moderate gene knockdown of bcat in Ap. glycines along with its associated phenotype. We also determined that the nanoparticle emulsion significantly increased the efficacy of gene knockdown. Overall, these results suggest that the aerosolized siRNA-nanoparticle delivery method is a promising new high-throughput and non-invasive RNAi delivery method in some aphid species.

  14. Aerosol and monsoon climate interactions over Asia

    NASA Astrophysics Data System (ADS)

    Li, Zhanqing; Lau, W. K.-M.; Ramanathan, V.; Wu, G.; Ding, Y.; Manoj, M. G.; Liu, J.; Qian, Y.; Li, J.; Zhou, T.; Fan, J.; Rosenfeld, D.; Ming, Y.; Wang, Y.; Huang, J.; Wang, B.; Xu, X.; Lee, S.-S.; Cribb, M.; Zhang, F.; Yang, X.; Zhao, C.; Takemura, T.; Wang, K.; Xia, X.; Yin, Y.; Zhang, H.; Guo, J.; Zhai, P. M.; Sugimoto, N.; Babu, S. S.; Brasseur, G. P.

    2016-12-01

    The increasing severity of droughts/floods and worsening air quality from increasing aerosols in Asia monsoon regions are the two gravest threats facing over 60% of the world population living in Asian monsoon regions. These dual threats have fueled a large body of research in the last decade on the roles of aerosols in impacting Asian monsoon weather and climate. This paper provides a comprehensive review of studies on Asian aerosols, monsoons, and their interactions. The Asian monsoon region is a primary source of emissions of diverse species of aerosols from both anthropogenic and natural origins. The distributions of aerosol loading are strongly influenced by distinct weather and climatic regimes, which are, in turn, modulated by aerosol effects. On a continental scale, aerosols reduce surface insolation and weaken the land-ocean thermal contrast, thus inhibiting the development of monsoons. Locally, aerosol radiative effects alter the thermodynamic stability and convective potential of the lower atmosphere leading to reduced temperatures, increased atmospheric stability, and weakened wind and atmospheric circulations. The atmospheric thermodynamic state, which determines the formation of clouds, convection, and precipitation, may also be altered by aerosols serving as cloud condensation nuclei or ice nuclei. Absorbing aerosols such as black carbon and desert dust in Asian monsoon regions may also induce dynamical feedback processes, leading to a strengthening of the early monsoon and affecting the subsequent evolution of the monsoon. Many mechanisms have been put forth regarding how aerosols modulate the amplitude, frequency, intensity, and phase of different monsoon climate variables. A wide range of theoretical, observational, and modeling findings on the Asian monsoon, aerosols, and their interactions are synthesized. A new paradigm is proposed on investigating aerosol-monsoon interactions, in which natural aerosols such as desert dust, black carbon from

  15. Simultaneous reductions in emissions of black carbon and co-emitted species will weaken the aerosol net cooling effect

    NASA Astrophysics Data System (ADS)

    Wang, Z. L.; Zhang, H.; Zhang, X. Y.

    2015-04-01

    Black carbon (BC), a distinct type of carbonaceous material formed from the incomplete combustion of fossil and biomass based fuels under certain conditions, can interact with solar radiation and clouds through its strong light-absorption ability, thereby warming the Earth's climate system. Some studies have even suggested that global warming could be slowed down in the short term by eliminating BC emission due to its short lifetime. In this study, we estimate the influence of removing some sources of BC and other co-emitted species on the aerosol radiative effect by using an aerosol-climate atmosphere-only model BCC_AGCM2.0.1_CUACE/Aero with prescribed sea surface temperature and sea ice cover, in combination with the aerosol emissions from the Representative Concentration Pathways (RCPs) scenarios. We find that the global annual mean aerosol net cooling effect at the top of the atmosphere (TOA) will be enhanced by 0.12 W m-2 compared with recent past year 2000 levels if the emissions of only BC are reduced to the level projected for 2100 based on the RCP2.6 scenario. This will be beneficial~for the mitigation of global warming. However, both aerosol negative direct and indirect radiative effects are weakened when BC and its co-emitted species (sulfur dioxide and organic carbon) are simultaneously reduced. Relative to year 2000 levels, the global annual mean aerosol net cooling effect at the TOA will be weakened by 1.7-2.0 W m-2 if the emissions of all these aerosols are decreased to the levels projected for 2100 in different ways based on the RCP2.6, RCP4.5, and RCP8.5 scenarios. Because there are no effective ways to remove the BC exclusively without influencing the other co-emitted components, our results therefore indicate that a reduction in BC emission can lead to an unexpected warming on the Earth's climate system in the future.

  16. Change in the amount of epsilon-hexosyllysine, UV absorbance, and fluorescence of collagen with age in different animal species

    SciTech Connect

    Miksik, I.; Deyl, Z. )

    1991-05-01

    Skin and aorta collagen specimens of Wistar rats, white mice, beagle dogs, cats, horses, and human necropsies of different ages were examined with respect to the content of glycated products. The data presented show that (a) glycation and accumulation of the chromophore(s) are comparable in collagen samples from different species of comparable age; (b) glycation and pigmented accumulation increase markedly during the first 5-10 years of age; (c) the extent of glycation is different in different tissues (in particular, glycation of aortal collagen is about twice that of skin collagen); and (d) collagen pigmentation as followed by fluorescence is comparable in aortal and skin collagen (except below 10 years); pigmentation measured by absorbance at 350 nm is, on the contrary, lower in aortal than in skin collagen. Based on the assumption of constant blood glucose level during the life span, it appears feasible to conclude that the degree of nonenzymatic collagen glycation reflects the time period for which the protein was exposed to the action of sugars. This period, because of increased cross-linking, is likely to be extended in older animals. Other factors, such as differences in collagen turnover between different tissues and the intensity of the removal process of the glycated products, should be taken into consideration as well.

  17. Ion mobility spectrometry-mass spectrometry (IMS-MS) for on- and offline analysis of atmospheric gas and aerosol species

    NASA Astrophysics Data System (ADS)

    Krechmer, Jordan E.; Groessl, Michael; Zhang, Xuan; Junninen, Heikki; Massoli, Paola; Lambe, Andrew T.; Kimmel, Joel R.; Cubison, Michael J.; Graf, Stephan; Lin, Ying-Hsuan; Budisulistiorini, Sri H.; Zhang, Haofei; Surratt, Jason D.; Knochenmuss, Richard; Jayne, John T.; Worsnop, Douglas R.; Jimenez, Jose-Luis; Canagaratna, Manjula R.

    2016-07-01

    Measurement techniques that provide molecular-level information are needed to elucidate the multiphase processes that produce secondary organic aerosol (SOA) species in the atmosphere. Here we demonstrate the application of ion mobility spectrometry-mass spectrometry (IMS-MS) to the simultaneous characterization of the elemental composition and molecular structures of organic species in the gas and particulate phases. Molecular ions of gas-phase organic species are measured online with IMS-MS after ionization with a custom-built nitrate chemical ionization (CI) source. This CI-IMS-MS technique is used to obtain time-resolved measurements (5 min) of highly oxidized organic molecules during the 2013 Southern Oxidant and Aerosol Study (SOAS) ambient field campaign in the forested SE US. The ambient IMS-MS signals are consistent with laboratory IMS-MS spectra obtained from single-component carboxylic acids and multicomponent mixtures of isoprene and monoterpene oxidation products. Mass-mobility correlations in the 2-D IMS-MS space provide a means of identifying ions with similar molecular structures within complex mass spectra and are used to separate and identify monoterpene oxidation products in the ambient data that are produced from different chemical pathways. Water-soluble organic carbon (WSOC) constituents of fine aerosol particles that are not resolvable with standard analytical separation methods, such as liquid chromatography (LC), are shown to be separable with IMS-MS coupled to an electrospray ionization (ESI) source. The capability to use ion mobility to differentiate between isomers is demonstrated for organosulfates derived from the reactive uptake of isomers of isoprene epoxydiols (IEPOX) onto wet acidic sulfate aerosol. Controlled fragmentation of precursor ions by collisionally induced dissociation (CID) in the transfer region between the IMS and the MS is used to validate MS peak assignments, elucidate structures of oligomers, and confirm the

  18. Ion mobility spectrometry–mass spectrometry (IMS–MS) for on- and offline analysis of atmospheric gas and aerosol species

    DOE PAGES

    Krechmer, Jordan E.; Groessl, Michael; Zhang, Xuan; ...

    2016-07-25

    Measurement techniques that provide molecular-level information are needed to elucidate the multiphase processes that produce secondary organic aerosol (SOA) species in the atmosphere. Here we demonstrate the application of ion mobility spectrometry-mass spectrometry (IMS–MS) to the simultaneous characterization of the elemental composition and molecular structures of organic species in the gas and particulate phases. Molecular ions of gas-phase organic species are measured online with IMS–MS after ionization with a custom-built nitrate chemical ionization (CI) source. This CI–IMS–MS technique is used to obtain time-resolved measurements (5 min) of highly oxidized organic molecules during the 2013 Southern Oxidant and Aerosol Study (SOAS) ambientmore » field campaign in the forested SE US. The ambient IMS–MS signals are consistent with laboratory IMS–MS spectra obtained from single-component carboxylic acids and multicomponent mixtures of isoprene and monoterpene oxidation products. Mass-mobility correlations in the 2-D IMS–MS space provide a means of identifying ions with similar molecular structures within complex mass spectra and are used to separate and identify monoterpene oxidation products in the ambient data that are produced from different chemical pathways. Water-soluble organic carbon (WSOC) constituents of fine aerosol particles that are not resolvable with standard analytical separation methods, such as liquid chromatography (LC), are shown to be separable with IMS–MS coupled to an electrospray ionization (ESI) source. The capability to use ion mobility to differentiate between isomers is demonstrated for organosulfates derived from the reactive uptake of isomers of isoprene epoxydiols (IEPOX) onto wet acidic sulfate aerosol. Controlled fragmentation of precursor ions by collisionally induced dissociation (CID) in the transfer region between the IMS and the MS is used to validate MS peak assignments, elucidate structures of

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

    PubMed

    Ramachandran, S; Srivastava, Rohit

    2013-05-01

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

  20. The use of ambient measurements to identify which precursor species limit aerosol nitrate formation.

    PubMed

    Blanchard, C L; Roth, P M; Tanenbaum, S J; Ziman, S D; Seinfeld, J H

    2000-12-01

    A thermodynamic equilibrium model was used to investigate the response of aerosol NO3 to changes in concentrations of HNO3, NH3, and H2SO4. Over a range of temperatures and relative humidities (RHs), two parameters provided sufficient information for indicating the qualitative response of aerosol NO3. The first was the excess of aerosol NH4+ plus gas-phase NH3 over the sum of HNO3, particulate NO3, and particulate SO4(2-) concentrations. The second was the ratio of particulate to total NO3 concentrations. Computation of these quantities from ambient measurements provides a means to rapidly analyze large numbers of samples and identify cases in which inorganic aerosol NO3 formation is limited by the availability of NH3. Example calculations are presented using data from three field studies. The predictions of the indicator variables and the equilibrium model are compared.

  1. Optical Properties of Polymers Relevant to Secondary Organic Aerosols

    NASA Astrophysics Data System (ADS)

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

    2014-12-01

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

  2. An automated online instrument to quantify aerosol-bound reactive oxygen species (ROS) for ambient measurement and health-relevant aerosol studies

    NASA Astrophysics Data System (ADS)

    Wragg, Francis P. H.; Fuller, Stephen J.; Freshwater, Ray; Green, David C.; Kelly, Frank J.; Kalberer, Markus

    2016-10-01

    The adverse health effects associated with ambient aerosol particles have been well documented, but it is still unclear which aerosol properties are most important for their negative health impact. Some studies suggest the oxidative effects of particle-bound reactive oxygen species (ROS) are potential major contributors to the toxicity of particles. Traditional ROS measurement techniques are labour-intensive, give poor temporal resolution and generally have significant delays between aerosol sampling and ROS analysis. However, many oxidising particle components are reactive and thus potentially short-lived. Thus, a technique to quantify particle-bound ROS online would be beneficial to quantify also the short-lived ROS components. We introduce a new portable instrument to allow online, continuous measurement of particle-bound ROS using a chemical assay of 2'7'-dichlorofluorescein (DCFH) with horseradish peroxidase (HRP), via fluorescence spectroscopy. All components of the new instrument are attached to a containing shell, resulting in a compact system capable of automated continuous field deployment over many hours or days. From laboratory measurements, the instrument was found to have a detection limit of ˜ 4 nmol [H2O2] equivalents per cubic metre (m3) air, a dynamic range up to at least ˜ 2000 nmol [H2O2] equivalents per m3 air and a time resolution of ≤ 12 min. The instrument allows for ˜ 16 h automated measurement if unattended and shows a fast response to changes in concentrations of laboratory-generated oxidised organic aerosol. The instrument was deployed at an urban site in London, and particulate ROS levels of up to 24 nmol [H2O2] equivalents per m3 air were detected with PM2.5 concentrations up to 28 µg m-3. The new and portable Online Particle-bound ROS Instrument (OPROSI) allows fast-response quantification; this is important due to the potentially short-lived nature of particle-bound ROS as well as fast-changing atmospheric conditions

  3. Properties and sources of individual particles and some chemical species in the aerosol of a metropolitan underground railway station

    NASA Astrophysics Data System (ADS)

    Salma, Imre; Pósfai, Mihály; Kovács, Kristóf; Kuzmann, Ernő; Homonnay, Zoltán; Posta, József

    Aerosol samples in PM 10-2.0 and PM 2.0 size fractions were collected on the platform of a metropolitan underground railway station in central Budapest. Individual aerosol particles were studied using atomic force microscopy, scanning electron microscopy and transmission electron microscopy with energy-dispersive X-ray spectrometry and electron diffraction. The bulk aerosol samples were investigated by 57Fe Mössbauer spectroscopy, and they were subjected to chemical speciation analysis for Cr. The particles were classified into groups of iron oxides and iron, carbonates, silicates, quartz and carbonaceous debris. Electron micrographs showed that the Fe-rich particles in the PM 2.0 size fraction typically consisted of aggregates of nano-sized hematite crystals that were randomly oriented, had round shapes and diameters of 5-15 nm. In addition to hematite, a minor fraction of the iron oxide particles also contained magnetite. In addition, the PM 2.0-fraction particles typically had a rugged surface with layered or granular morphologies. Mössbauer spectroscopy suggested that hematite was a major Fe-bearing species in the PM 10-2.0 size fraction; its mass contribution to the Fe was 36%. Further constituents (ferrite, carbides and FeOOH) were also identified. The water soluble amounts of Cr for the underground railway station and city center were similar. In the PM 10-2.0 size fraction, practically all dissolved Cr had an oxidation state of three, which corresponds to ambient conditions. In the PM 2.0 size fraction, however, approximately 7% of the dissolved Cr was present as Cr(VI), which was different from that for the urban aerosol. It is suggested that the increased adverse health effects of aerosol particles in metros with respect to ambient outdoor particles is linked to the differences in the oxidation states, surface properties or morphologies.

  4. Hazardous components and health effects of atmospheric aerosol particles: reactive oxygen species, soot, polycyclic aromatic compounds and allergenic proteins.

    PubMed

    Shiraiwa, Manabu; Selzle, Kathrin; Pöschl, Ulrich

    2012-08-01

    This review outlines recent advances in the investigation of the chemical properties, molecular interactions and health effects of hazardous compounds in atmospheric aerosols, in particular reactive oxygen species (ROS), soot, polycyclic aromatic compounds (PACs) and allergenic proteins. Epidemiological studies show correlations between air particulate matter and adverse health effects of air pollution including allergy, asthma, cardiovascular and respiratory diseases, but the causative relations and mechanisms of interaction on the molecular level are still unclear. ROS generated by photochemical and heterogeneous reactions in the atmosphere seem to play a key role in aerosol health effects and provide a direct link between atmospheric and physiological multiphase processes. Soot and PACs can trigger formation of ROS in vivo, leading to inflammation and cellular damage. PACs as well as allergenic proteins are efficiently oxygenated and nitrated upon exposure to ozone and nitrogen dioxide, which leads to an enhancement of their toxicity and allergenicity.

  5. Global modeling of nitrate and ammonium aerosols using EQSAM3

    NASA Astrophysics Data System (ADS)

    Xu, L.; Penner, J. E.

    2009-12-01

    Atmospheric aerosols, particles suspending in air, are important as they affect human health, air quality, and visibility as well as climate. Sulfate, nitrate, ammonium, chloride and sodium are among the most important inorganic aerosol species in the atmosphere. These compounds are hygroscopic and absorb water under almost all ambient environmental conditions. The uptake of water alters the aerosol size, and causes water to become the constituent with the largest atmospheric aerosol mass, especially when the aerosols grow into fog, haze or clouds. Furthermore, several global model studies have demonstrated that rapid increases in nitrogen emissions could produce enough nitrate in aerosols to offset the expected decline in sulfate forcing by 2100 for the extreme IPCC A2 scenario (Bauer et al., 2007). Although nitrate and ammonium were identified as significant anthropogenic sources of aerosols by a number of modeling studies, most global aerosol models still exclude ammonium-nitrate when the direct aerosol forcing is studied. In this study, the computationally efficient equilibrium model, EQSAM3, is incorporated into the UMICH-IMPACT-nitrate model using the hybrid dynamical solution method (Feng and Penner, 2007). The partitioning of nitrate and ammonium along with the corresponding water uptake is evaluated by comparing the model to the EQUISOLVE II method used in Feng and Penner (2007). The model is also evaluated by comparison with the AERONET data base and satellite-based aerosol optical depths.

  6. Estimates of aerosol species scattering characteristics as a function of relative humidity

    NASA Astrophysics Data System (ADS)

    Malm, William C.; Day, Derek E.

    The absorption of water by ambient aerosols can significantly increase the light scattering coefficient and thereby affect issues such as visibility and climate forcing. Although water absorption by inorganic compounds and mixtures of inorganic compounds can often be modeled with adequate certainty for most applications, modeling water uptake by organic aerosols at present is speculative. In this paper, we present data in the form of f (RH)=b scat(RH)/b scat,dry , where bscat(RH) is the scattering coefficient measured at some relative humidity (RH)>20% and bscat,dry is the scattering coefficient measured at RH <20%. The f(RH) has been measured at Great Smoky Mountains National Park in Tennessee and at Grand Canyon National Park in Arizona. The f(RH) curves obtained from these two sites, which show distinctly different aerosol composition and average RH values, are compared. We also present comparisons between the measured water uptake by ambient aerosol with modeled water uptake by inorganic compounds to estimate the water uptake by organic aerosol.

  7. Formic Sulfuric Anhydride: a New Chemical Species with Possible Implications for Atmospheric Aerosol

    NASA Astrophysics Data System (ADS)

    Mackenzie, Becca; Dewberry, Chris; Leopold, Ken

    2015-06-01

    Aerosols are important players in the Earth's atmosphere, affecting climate, cloud formation, and human health. In this work, we report the discovery of a previously unknown molecule, formic sulfuric anhydride (FSA), that may influence the formation and composition of atmospheric aerosol particles. Five isotopologues of FSA have been observed by microwave spectroscopy and further characterized using DFT calculations. The system has dipole moment components along all three inertial axes, and indeed a, b, and c-type transitions have been observed. A π2 + π2 + σ2 cycloaddition reaction between SO3 and HCOOH is proposed as a possible mechanism for the formation of FSA and calculations indicate that the transformation is effectively barrierless. Facile formation of the anhydride followed by hydrolysis in small water-containing clusters or liquid droplets may provide a mechanism of incorporating volatile organics into atmospheric aerosol. We suggest that FSA and its derivatives be considered in future atmospheric and climate models.

  8. E-Cigarette Aerosol Exposure Induces Reactive Oxygen Species, DNA Damage, and Cell Death in Vascular Endothelial Cells.

    PubMed

    Anderson, Chastain; Majeste, Andrew; Hanus, Jakub; Wang, Shusheng

    2016-12-01

    Cigarette smoking remains one of the leading causes of preventable death worldwide. Vascular cell death and dysfunction is a central or exacerbating component in the majority of cigarette smoking related pathologies. The recent development of the electronic nicotine delivery systems known as e-cigarettes provides an alternative to conventional cigarette smoking; however, the potential vascular health risks of e-cigarette use remain unclear. This study evaluates the effects of e-cigarette aerosol extract (EAE) and conventional cigarette smoke extract (CSE) on human umbilical vein endothelial cells (HUVECs). A laboratory apparatus was designed to produce extracts from e-cigarettes and conventional cigarettes according to established protocols for cigarette smoking. EAE or conventional CSE was applied to human vascular endothelial cells for 4-72 h, dependent on the assay. Treated cells were assayed for reactive oxygen species, DNA damage, cell viability, and markers of programmed cell death pathways. Additionally, the anti-oxidants α-tocopherol and n-acetyl-l-cysteine were used to attempt to rescue e-cigarette induced cell death. Our results indicate that e-cigarette aerosol is capable of inducing reactive oxygen species, causing DNA damage, and significantly reducing cell viability in a concentration dependent fashion. Immunofluorescent and flow cytometry analysis indicate that both the apoptosis and programmed necrosis pathways are triggered by e-cigarette aerosol treatment. Additionally, anti-oxidant treatment provides a partial rescue of the induced cell death, indicating that reactive oxygen species play a causal role in e-cigarette induced cytotoxicity.

  9. Global three-dimensional simulation and radiative forcing of various aerosol species with GCM

    NASA Astrophysics Data System (ADS)

    Takemura, Toshihiko; Okamoto, Hajime; Numaguti, Atusi; Suzuki, Kentaroh; Higurashi, Akiko; Nakajima, Teruyuki

    2001-02-01

    A global three-dimensional transport model that can simultaneously treat main tropospheric aerosols, i.e., carbonaceous (organic and black carbons), sulfate, soil dust, and sea salt, is developed. It is coupled with a Center for Climate System Research (CCSR)/National Institute for Enviormental Studies (NIES) atmospheric general circulation model (AGCM), and the meteorological field of wind, temperature, and specific humidity can be nudged by reanalysis data. Simulated results are compared with not only observations for aerosol concentrations but also the optical thickness and Angstrom exponent retrieved from remote sensing data such as National Oceanic and Atmospheric Administration (NOAA)/Advanced Very High Resolution Radiometer (AVHRR) and Aerosol Robotic Network (AERONET). A general agreement is found between simulated results and observations spatially seasonally, and quantitatively. The present model is also coupled with the radiative process over both the solar and thermal regions. The annual and global mean radiative forcing by anthropogenic aerosols from fossil fuel sources is estimated to be -0.5 W m-2 over the clear sky for the direct effect and -2.0 W m-2 for the indirect effect.

  10. Atmospheric responses to stratospheric aerosol geoengineering

    NASA Astrophysics Data System (ADS)

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

    2013-04-01

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

  11. Emissions of biogenic volatile organic compounds and subsequent photochemical production of secondary organic aerosol in mesocosm studies of temperate and tropical plant species

    NASA Astrophysics Data System (ADS)

    Wyche, K. P.; Ryan, A. C.; Hewitt, C. N.; Alfarra, M. R.; McFiggans, G.; Carr, T.; Monks, P. S.; Smallbone, K. L.; Capes, G.; Hamilton, J. F.; Pugh, T. A. M.; MacKenzie, A. R.

    2014-12-01

    Silver birch (Betula pendula) and three Southeast Asian tropical plant species (Ficus cyathistipula, Ficus benjamina and Caryota millis) from the pantropical fig and palm genera were grown in a purpose-built and environment-controlled whole-tree chamber. The volatile organic compounds emitted from these trees were characterised and fed into a linked photochemical reaction chamber where they underwent photo-oxidation under a range of controlled conditions (relative humidity or RH ~65-89%, volatile organic compound-to-NOx or VOC / NOx ~3-9 and NOx ~2 ppbV). Both the gas phase and the aerosol phase of the reaction chamber were monitored in detail using a comprehensive suite of on-line and off-line chemical and physical measurement techniques. Silver birch was found to be a high monoterpene and sesquiterpene but low isoprene emitter, and its emissions were observed to produce measurable amounts of secondary organic aerosol (SOA) via both nucleation and condensation onto pre-existing seed aerosol (YSOA 26-39%). In contrast, all three tropical species were found to be high isoprene emitters with trace emissions of monoterpenes and sesquiterpenes. In tropical plant experiments without seed aerosol there was no measurable SOA nucleation, but aerosol mass was shown to increase when seed aerosol was present. Although principally isoprene emitting, the aerosol mass produced from tropical fig was mostly consistent (i.e. in 78 out of 120 aerosol mass calculations using plausible parameter sets of various precursor specific yields) with condensation of photo-oxidation products of the minor volatile organic compounds (VOCs) co-emitted; no significant aerosol yield from condensation of isoprene oxidation products was required in the interpretations of the experimental results. This finding is in line with previous reports of organic aerosol loadings consistent with production from minor biogenic VOCs co-emitted with isoprene in principally isoprene-emitting landscapes in Southeast

  12. Analysis of the Body Distribution of Absorbed Dose in the Organs of Three Species of Fish from Sepetiba Bay

    NASA Astrophysics Data System (ADS)

    Pereira, Wagner de S.; Kelecom, Alphonse; dos Santos Gouvea, Rita de Cássia; Py Júnior, Delcy de Azevedo

    2008-08-01

    The body distribution of Polonium-210 in three fishes from the Sepetiba Bay (Macrodon ancylodon, Micropogonias furnieri and Mugil curema) has been studied under the approach of the Department of Energy of the United States of America (DOE) that set the limit of absorbed dose rate in biota equal to 3.5×103 μGy/y, and that also established the relation between dose rate (D) and radionuclide concentration (c) on a fish muscle fresh weight basis, as follows: D = 5.05 E×N×C, assuming that the radionuclide distribution is homogenous among organs. Two hypotheses were tested here, using statistical tools: 1) is the body distribution of absorbed dose homogenous among organs? and 2) is the body distribution of absorbed dose identical among studied fishes? It was concluded, as expected, that the distribution among organs is heterogeneous; but, unexpectedly, that the three fishes display identical body distribution pattern, although they belong to different trophic levels. Hence, concerning absorbed dose calculation, the statement that data distribution is homogenous must be understood merely as an approximation, at least in the case of Polonium-210.

  13. Analysis of the Body Distribution of Absorbed Dose in the Organs of Three Species of Fish from Sepetiba Bay

    SciTech Connect

    Pereira, Wagner de S; Kelecom, Alphonse; Santos Gouvea, Rita de Cassia dos; Azevedo Py Junior, Delcy de

    2008-08-07

    The body distribution of Polonium-210 in three fishes from the Sepetiba Bay (Macrodon ancylodon, Micropogonias furnieri and Mugil curema) has been studied under the approach of the Department of Energy of the United States of America (DOE) that set the limit of absorbed dose rate in biota equal to 3.5x10{sup 3} {mu}Gy/y, and that also established the relation between dose rate (D) and radionuclide concentration (c) on a fish muscle fresh weight basis, as follows: D = 5.05 ExNxC, assuming that the radionuclide distribution is homogenous among organs. Two hypotheses were tested here, using statistical tools: 1) is the body distribution of absorbed dose homogenous among organs? and 2) is the body distribution of absorbed dose identical among studied fishes? It was concluded, as expected, that the distribution among organs is heterogeneous; but, unexpectedly, that the three fishes display identical body distribution pattern, although they belong to different trophic levels. Hence, concerning absorbed dose calculation, the statement that data distribution is homogenous must be understood merely as an approximation, at least in the case of Polonium-210.

  14. High-Resolution Modeling of the Predictability of Convective Systems, and Influences by Absorbing Aerosols Over Northern India and the Himalayas Foothills During Boreal Summer

    NASA Technical Reports Server (NTRS)

    Kim, Kyu-Myong; Lau, William K.-M.; Tao, Wei-Kuo; Shi, Jainn; Tan, Qian; Chin, Mian; Matsui, Toshihisa; Bian, Huisheng

    2011-01-01

    The Himalayas foothills region (HFR) is an important component of the South Asian monsoon. To the south, the HFR borders the fertile, populous, and heavily polluted Indo-Gangetic Plain (IGP). To the north, it rises to great height (approx. 4-5 km) to the Tibetan Plateau over a distance of less than 100 km. The HFR itself consists of complex mountainous terrain, with strong orographic forcing for precipitation. During the late spring and early summer, dust aerosol from the Thar and Middle East deserts , as well as moisture from the Arabian Sea were transported to the western part of the western part of the IGP and foothills spurs pre-monsoon severe thunderstorm over the region. During the monsoon season (mid June -August) convection from the Bay of Bengal, spread along the foothills northwestward to northern Pakistan. Recent climate model studies and preliminary observations have indicted not only the importance of dynamical forcing of precipitation in the HFR, but also possible strong impacts by the dense aerosols, from both local sources, and remote transport, that blanket the IGP from late spring up to the onset of the monsoon in June, and during monsoon breaks in July. In this work, we use the NASA Unified Weather Research and Forecasting (Nu-WRF) model to study the predictability ( 1-7 days) South Asian monsoon rainfall system. Results of 7 -day forecast experiments using an embedded domain of 27 km and 9 km resolution were conducted for the period June 11- July 15, 2008, with and without aerosol forcing are carried out to assess the intrinsic predictability of rainfall over the HFR, and possible impacts by aerosol direct effect, and possible connection of large-scale South Asian monsoon system.

  15. Influence of Aerosols on Monsoon Circulation and Hydroclimate

    NASA Technical Reports Server (NTRS)

    Lau, William K.

    2006-01-01

    Long recognized as a major environmental hazard, aerosol is now known to have strong impacts on both regional and global water cycles and climate change. In the Asian monsoon regions, the response of the regional water cycle and climate to aerosol forcing is very complex, not only because of presence of diverse mix of aerosol species with vastly different radiative properties, but also because the monsoon is strongly influenced by ocean and land surface processes, land use, land change, as well as regional and global greenhouse warming effects. Thus, sorting out the impacts of aerosol forcing, and interaction with the monsoon water cycle is a very challenging problem. Up to now, besides the general notion that aerosols may significantly impact monsoon through altering large scale radiative heating gradients, there has been very little information regarding the specific signatures, and mechanisms of aerosol-monsoon water cycle interaction. In this talk, based on preliminary results from observations and climate model experiments, I will offer some insights into how aerosols may impact the Asian monsoon water cycle, in particular the effects of absorbing aerosols (dust and black carbon), and the role of the Tibetan Plateau. The influence of aerosol forcing relative to those due to sea surface temperature and land surface processes, and impact on potential predictability of the monsoon climate system will also be discussed.

  16. Influence of Aerosols on Monsoon Circulation and Hydroclimate

    NASA Technical Reports Server (NTRS)

    Lau, William K.M.

    2007-01-01

    Long recognized as a major environmental hazard, aerosol is now known to have strong impacts on both regional and global water cycles and climate change. In the Asian monsoon regions, the response of the regional water cycle and climate to aerosol forcing is very complex, not only because of presence of diverse mix of aerosol species with vastly different radiative properties, but also because the monsoon is strongly influenced by ocean and land surface processes, land use, land change, as well as regional and global greenhouse warming effects. Thus, sorting out the impacts of aerosol forcing, and interaction with the monsoon water cycle is a very challenging problem. Up to now, besides the general notion that aerosols may significantly impact monsoon through altering large scale radiative heating gradients, there has been very little information regarding the specific signatures, and mechanisms of aerosol-monsoon water cycle interaction. In this talk, based on preliminary results from observations and climate model experiments, I will offer some insights into how aerosols may impact the Asian monsoon water cycle, in particular the effects of absorbing aerosols (dust and black carbon), and the role of the Tibetan Plateau. The influence of aerosol forcing relative to those due to sea surface temperature and land surface processes, and impact on potential predictability of the monsoon climate system will also be discussed.

  17. Solar Occultation Constellation for Retrieving Aerosols and Trace Element Species (SOCRATES) Mission Concept

    NASA Astrophysics Data System (ADS)

    Bailey, S. M.; Bevilacqua, R. M.; Fish, C. S.; Gordley, L. L.; Fromm, M. D.

    2014-12-01

    The goal of SOCRATES is to quantify the critical role of the upper troposphere/lower stratosphere (UTLS) in the climate system. The mission would provide, for the first time, the suite of measurements required to quantify stratosphere/troposphere exchange (STE) pathways and their contribution to UTLS composition, and to evaluate the radiative forcing implications of potential changes in STE pathways with climate change. The discrimination and quantification of STE pathways requires simultaneous measurement of several key trace gases and aerosols with high precision, accuracy, and vertical resolution. Furthermore, aerosol and clouds, often present in the UTLS, complicate the measurement of trace gases. The SOCRATES sensor is a 23-channel Gas Filter Correlation Radiometer (GFCR), referred to as GLO (GFCR Limb solar Occultation), with heritage from HALOE on UARS, and SOFIE on AIM. GLO measures aerosol extinction from 0.45 to 3.88 μm, important radiatively active gases in the UTLS (H2O, O3, CH4, N2O), key tracers of STE (HCN, CO, HDO), gases important in stratospheric O3 chemistry (HCl and HF), and temperature from cloud top to 50 km at a vertical resolution of 1 km. Improved pointing knowledge will provide dramatically better retrieval precision in the UTLS, even in the presence of aerosols, than possible with HALOE. In addition, the GLO form factor is only a few percent of that of HALOE, and costs for a constellation of GLO sensors is within the cost cap of a NASA Venture mission. The SOCRATES mission concept is an 8-element constellation of autonomous CubeSats, each mated with a GLO sensor, deployed from a single launch vehicle. The SOCRATES/GLO approach reaps the advantages of solar occultation: high precision and accuracy; robust calibration; and high vertical resolution, while mitigating the sparse coverage of a single solar occultation sensor. We present the SOCRATES science case, and key elements of the SOCRATES mission and GLO instrument concepts.

  18. Solar Occultation Constellation for Retrieving Aerosols and Trace Element Species (SOCRATES): Proposed Mission Concept

    NASA Astrophysics Data System (ADS)

    Gordley, L. L.; Bailey, S. M.

    2015-12-01

    The goal of SOCRATES is to resolve the critical but underexplored role of the upper troposphere/lower stratosphere (UTLS) in climate change. The mission would provide the suite of measurements required to quantify UTLS transport pathways and their contribution to UTLS composition, and to evaluate the radiative forcing implications of changes in UTLS composition forced by expected changes in these pathways as the climate evolves. The discrimination and quantification of UTLS transport pathways requires simultaneous measurement of several key trace gases and aerosols with high precision, accuracy, and vertical resolution. Furthermore, aerosols and clouds, often present in the UTLS, complicate the measurement of trace gases. The SOCRATES sensor is a 23-channel Gas Filter Correlation Radiometer (GFCR), referred to as GLO (GFCR Limb solar Occultation), with heritage from HALOE on UARS, and SOFIE on AIM. GLO measures aerosol extinction from 0.45 to 3.88 μm, important radiatively active gases in the UTLS (H2O, O3, CH4, N2O), key tracers of UTLS transport (HCN, CO, HDO), gases important in stratospheric O3 chemistry (HCl and HF), and temperature from cloud top to 50 km at a vertical resolution of < 1 km. Improved pointing knowledge will provide dramatically better retrieval precision in the UTLS, even in the presence of aerosols, than possible with HALOE. In addition, the GLO form factor is only of order 10% of that of HALOE, and costs for a constellation of GLO sensors is within the cost cap of a NASA Earth Venture mission. The SOCRATES mission concept is a 6-element constellation of autonomous small satellites, each mated with a GLO sensor, and deployed from a single launch vehicle. The SOCRATES/GLO approach reaps the advantages of solar occultation: high precision and accuracy; robust calibration; and high vertical resolution, while mitigating the sparse coverage of a single solar occultation sensor. We present the SOCRATES science case, and key elements of the

  19. Measurements of HNO3, SO2 High Resolution Aerosol SO4 (sup 2-), and Selected Aerosol Species Aboard the NASA DC-8 Aircraft: During the Transport and Chemical Evolution Over the Pacific Airborne Mission (TRACE-P)

    NASA Technical Reports Server (NTRS)

    Talbot, Robert W.; Dibb, Jack E.

    2004-01-01

    The UNH investigation during TRACE-P provided measurements of selected acidic gases and aerosol species aboard the NASA DC-8 research aircraft. Our investigation focused on measuring HNO3, SO2, and fine (less than 2 microns) aerosol SO4(sup 2-) with two minute time resolution in near-real-time. We also quantified mixing ratios of aerosol ionic species, and aerosol (210)Pb and (7)Be collected onto bulk filters at better than 10 minute resolution. This suite of measurements contributed extensively to achieving the principal objectives of TRACE-P. In the context of the full data set collected by experimental teams on the DC-8, our observations provide a solid basis for assessing decadal changes in the chemical composition and source strength of Asian continental outflow. This region of the Pacific should be impacted profoundly by Asian emissions at this time with significant degradation of air quality over the next few decades. Atmospheric measurements in the western Pacific region will provide a valuable time series to help quantify the impact of Asian anthropogenic activities. Our data also provide important insight into the chemical and physical processes transforming Asian outflow during transport over the Pacific, particularly uptake and reactions of soluble gases on aerosol particles. In addition, the TRACE-P data set provide strong constraints for assessing and improving the chemical fields simulated by chemical transport models.

  20. Single-Species Aerosol Coagulation and Deposition with Arbitrary Size Resolution.

    SciTech Connect

    SAJO, ERNO

    2012-07-31

    Version 00 SAEROSA solves the dynamic aerosol coagulation and deposition problem with arbitrary computational precision under a variety of conditions. The code includes numerous user-selectable coagulation kernels, alone or in combinations, and permits an arbitrary initial size distribution. Many parameter combinations and what-if scenarios under user control are possible. The output gives the particle size distribution suspended in the carrier fluid initially and after the desired aerosol aging time in terms of both differential and integral aerosol volume concentrations. An auxiliary routine designed for the Mac OSX environment provides plotting capability. The output can be further processed by e.g., spreadsheets. The code has been benchmarked against three computer models, including MAEROS, and analytical models with excellent agreement. The test cases also included scenarios where previously published computational coagulation models lack capabilities or exhibit numerical instabilities. These included narrow, delta function, and non-lognormal initial size distributions, and further conditions, such as the presence of simultaneous coagulation mechanisms, including electrostatic effects, spanning multiple flow-regimes.

  1. Effects of Aerosol on Atmospheric Dynamics and Hydrologic Processes During Boreal Spring and Summer

    NASA Technical Reports Server (NTRS)

    Lau, William K. M.; Kim, M. K.; Kim, K. M.; Chin, Mian

    2005-01-01

    Global and regional climate impacts of present-day aerosol loading during boreal spring are investigated using the NASA finite volume General Circulation Model (fvGCM). Three-dimensional distributions of loadings of five species of tropospheric aerosols, i.e., sulfate, black carbon, organic carbon, soil dust, and sea salt are prescribed from outputs of the Goddard Ozone Chemistry Aerosol Radiation and Transport model (GOCART). The aerosol loadings are used to calculate the extinction coefficient, single scattering albedo, and asymmetric factor at eleven spectral wavelengths in the radiative transfer code. We find that aerosol-radiative forcing during boreal spring excites a wavetrain-like pattern in tropospheric temperature and geopotential height that emanates from Northern Africa, through Eurasia, to northeastern Pacific. Associated with the teleconnection is strong surface cooling over regions with large aerosol loading, i.e., China, India, and Africa. Low-to-mid tropospheric heating due to shortwave absorption is found in regions with large loading of dust (Northern Africa, and central East Asia), and black carbon (South and East Asia). In addition pronounced surface cooling is found over the Caspian Sea and warming over Eurasian and northeastern Asia, where aerosol loadings are relatively low. These warming and cooling are components of teleconnection pattern produced primarily by atmospheric heating from absorbing aerosols, i.e., dust from North Africa and black carbon from South and East Asia. Effects of aerosols on atmospheric hydrologic cycle in the Asian monsoon region are also investigated. Results show that absorbing aerosols, i.e., black carbon and dust, induce large-scale upper-level heating anomaly over the Tibetan Plateau in April and May, ushering in an early onset of the Indian summer monsoon. Absorbing aerosols also enhance lower-level heating and anomalous ascent over northern India, intensifying the Indian monsoon. Overall, the aerosol

  2. Effects of Aerosol on Atmospheric Dynamics and Hydrologic Processes during Boreal Spring and Summer

    NASA Technical Reports Server (NTRS)

    Lau, William K. M.; Kim, M. K.; Chin, Mian; Kim, K. M.

    2005-01-01

    Global and regional climate impacts of present-day aerosol loading during boreal spring are investigated using the NASA finite volume General Circulation Model (fvGCM). Three-dimensional distributions of loadings of five species of tropospheric aerosols, i.e., sulfate, black carbon, organic carbon, soil dust, and sea salt are prescribed from outputs of the Goddard Ozone Chemistry Aerosol Radiation and Transport model (GOCART). The aerosol loadings are used to calculate the extinction coefficient, single scattering albedo, and asymmetric factor at eleven spectral wavelengths in the radiative transfer code. We find that aerosol-radiative forcing during boreal spring excites a wavetrain-like pattern in tropospheric temperature and geopotential height that emanates from Northern Africa, through Eurasia, to northeastern Pacific. Associated with the teleconnection is strong surface cooling over regions with large aerosol loading, i.e., China, India, and Africa. Low-to-mid tropospheric heating due to shortwave absorption is found in regions with large loading of dust (Northern Africa, and central East Asia), and black carbon (South and East Asia). In addition pronounced surface cooling is found over the Caspian Sea and warming over Eurasian and northeastern Asia, where aerosol loadings are relatively low. These warming and cooling are components of teleconnection pattern produced primarily by atmospheric heating from absorbing aerosols, i.e., dust from North Africa and.black carbon from South and East Asia. Effects of aerosols on atmospheric hydrologic cycle in the Asian monsoon region are also investigated. Results show that absorbing aerosols, i.e., black carbon and dust, induce large-scale upper-level heating anomaly over the Tibetan Plateau in April and May, ushering in an early onset of the Indian summer monsoon. Absorbing aerosols also enhance lower-level heating and anomalous ascent over northern India, intensifying the Indian monsoon. Overall, the aerosol

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

    SciTech Connect

    Dr. Timothy Onasch

    2009-09-09

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

  4. Emissions of biogenic volatile organic compounds and subsequent photochemical production of secondary organic aerosol in mesocosm studies of temperate and tropical plant species

    NASA Astrophysics Data System (ADS)

    Wyche, K. P.; Ryan, A. C.; Hewitt, C. N.; Alfarra, M. R.; McFiggans, G.; Carr, T.; Monks, P. S.; Smallbone, K. L.; Capes, G.; Hamilton, J. F.; Pugh, T. A. M.; MacKenzie, A. R.

    2014-06-01

    Silver birch (Betula pendula) and three Southeast Asian tropical plant species (Ficus cyathistipula, Ficus benjamina and Caryota millis) from the pantropical fig and palm genera were grown in a purpose-built and environment-controlled whole-tree chamber. The volatile organic compounds emitted from these trees were characterised and fed into a linked photochemical reaction chamber where they underwent photooxidation under a range of controlled conditions (RH ∼65-89%, VOC/NOx ∼3-9 and NOx ∼2 ppbV). Both the gas phase and the aerosol phase of the reaction chamber were monitored in detail using a comprehensive suite of on-line and off-line, chemical and physical measurement techniques. Silver birch was found to be a high monoterpene and sesquiterpene, but low isoprene emitter, and its emissions were observed to produce measureable amounts of SOA via both nucleation and condensation onto pre-existing seed aerosol (YSOA 26-39%). In contrast, all three tropical species were found to be high isoprene emitters with trace emissions of monoterpenes and sesquiterpenes. In tropical plant experiments without seed aerosol there was no measurable SOA nucleation, but aerosol mass was shown to increase when seed aerosol was present. Although principally isoprene emitting, the aerosol mass produced from tropical fig was mostly consistent (i.e., in 78 out of 120 aerosol mass calculations using plausible parameter sets of various precursor specific yields) with condensation of photooxidation products of the minor VOCs co-emitted; no significant aerosol yield from condensation of isoprene oxidation products was required in the interpretations of the experimental results. This finding is in line with previous reports of organic aerosol loadings consistent with production from minor biogenic VOCs co-emitted with isoprene in principally-isoprene emitting landscapes in Southeast Asia. Moreover, in general the amount of aerosol mass produced from the emissions of the principally

  5. Stress-induced biogenic VOC emissions from typical European tree species, their impact on secondary organic aerosol formation and possible climate feedbacks

    NASA Astrophysics Data System (ADS)

    Kleist, E.; Mentel, T. F.; Andres, S.; Dal Maso, M.; Hohaus, T.; Kindler-Scharr, A.; Rudich, Y.; Springer, M.; Tillmann, R.; Uerlings, R.; Wahner, A.; Wildt, J.

    2011-12-01

    Biogenic volatile organic compounds (BVOC) are precursors of secondary organic aerosols (SOA), which can scatter and absorb radiation. BVOC therefore indirectly impact the Earth's climate. Earth's climate is projected to change, possibly putting and vegetation under stress due to intensive heat and drought periods. Such stress situations will alter BVOC emissions that may induce feedbacks between vegetation and climate change. The main aim of our study is to determine whether such effect exists. A first step was to determine the impacts of drought and heat on BVOC emissions and subsequent SOA formation. Experiments were performed in the Juelich plant atmosphere chamber. Pine and Spruce were taken as representatives for species exhibiting storage organs for monoterpenes (MT). Beech and Birch were used as species with MT emissions closely coupled to CO2 uptake. The plants were stored under well-defined conditions of temperature and light intensity. Heat stress was induced by increasing the chamber temperature; drought stress was induced by not irrigating the plants. A fraction of the air leaving the plant chamber was fed into a reaction chamber where SOA formation was induced by OH-initiated oxidation. During stress situations the plants' BVOC emissions changed significantly. As a general feature we found that combined heat and drought stress increased MT emissions from conifers but decreased MT emissions from the broadleaf species. The former was attributed to a heat-induced breakdown of storage organs. The latter was attributed to a general breakdown of biosynthetic activity. SOA formation potentials were changed together with the MT emissions. The decrease in SOA formation potential due to the decrease of MT emissions from broadleaf species was amplified by additional emissions of green leaf volatiles (GLV). Obviously, GLV can suppress SOA formation by suppressing OH concentrations. GLV were also emitted from the conifers under heat stress. However the

  6. Release of Reactive Halogen Species from Sea-Salt Aerosols under Tropospheric Conditions with/without the Influence of Organic Matter in Smog-Chamber Experiments

    NASA Astrophysics Data System (ADS)

    Balzer, N.; Behnke, W.; Bleicher, S.; Krueger, H.; Ofner, J.; Siekmann, F.; Zetzsch, C.

    2008-12-01

    Experiments to investigate the release of reactive halogen species from sea-salt aerosol and the influence of organic matter were performed in an aerosol smog-chamber (3500 l), made of Teflon film (FEP 200A, Dupont). Smog chamber facilities at lowered temperature (coolable down to -25°C) enable us to simulate these reactions under polar, tropospheric conditions. First experiments were performed to investigate the production of atomic Br and Cl without the impact of organic aerosol. Br and Cl play an important role in atmospheric ozone depletion, particularly regarding ozone depletion events (bromine explosion) during polar spring. In these studies, the aerosol was generated by atomizing salt solutions containing the typical Br/Cl ratio of 1/660 in seawater by an ultrasonic nebulizer and increasing the Br content up to sixfold. To ensure the aqueous surface of the aerosol, the experiments were performed at relative humidities above 76%. We determined the atomic Cl and OH-radical concentrations from the simultaneous consumption of four reference hydrocarbons. The Br-radical concentration was calculated on the basis of ozone depletion. Organic aerosol may take part in these reaction cycles by halogenation and production of volatile organic halogens. Further experiments are planned to add organic aerosol for mechanistic and kinetic studies on the influence of secondary organic aerosols (SOA) and humic-like substances (HULIS) on bromine explosion. The formation of the secondary organic aerosol and the determination of possible halogenated gaseous and solid organic products will be studied using longpath-FTIR, DRIFTS, ATR-FTIR, GC-FID, GC-ECD, GC-MS, TPD-MS and DMA-CNC.

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

    NASA Astrophysics Data System (ADS)

    Xu, Lingling; Chen, Jinsheng

    2016-04-01

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

  8. Detailed mass size distributions of atmospheric aerosol species in the Negev desert, Israel, during ARACHNE-96

    NASA Astrophysics Data System (ADS)

    Maenhaut, Willy; Ptasinski, Jacek; Cafmeyer, Jan

    1999-04-01

    As part of the 1996 summer intensive of the Aerosol, RAdiation and CHemistry Experiment (ARACHNE-96), the mass size distribution of various airborne particulate elements was studied at a remote site in the Negev Desert, Israel. Aerosol collections were made with 8-stage PIXE International cascade impactors (PCIs) and 12-stage small deposit area low pressure impactors (SDIs) and the samples were analyzed by PIXE for about 20 elements. The mineral elements (Al, Si, Ca, Ti, Fe) exhibited a unimodal size distribution which peaked at about 6 μm, but the contribution of particles larger than 10 μm was clearly more pronounced during the day than during night. Sulphur and Br had a tendency to exhibit two modes in the submicrometer size range, with diameters at about 0.3 and 0.6 μm, respectively. The elements V and Ni, which are indicators of residual fuel burning, showed essentially one fine mode (at 0.3 μm) in addition to a coarse mode which represented the mineral dust contribution. Overall, good agreement was observed between the mass size distributions from the PCI and SDI devices. The PCI was superior to the SDI for studying the size distribution in the coarse size range, but the SDI was clearly superior for unravelling the various modes in the submicrometer size range.

  9. The Regional Environmental Impacts of Atmospheric Aerosols over Egypt

    NASA Astrophysics Data System (ADS)

    Zakey, Ashraf; Ibrahim, Alaa

    2015-04-01

    Identifying the origin (natural versus anthropogenic) and the dynamics of aerosols over Egypt at varying temporal and spatial scales provide valuable knowledge on the regional climate impacts of aerosols and their ultimate connections to the Earth's regional climate system at the MENA region. At regional scale, Egypt is exposed to air pollution with levels exceeding typical air-quality standards. This is particularly true for the Nile Delta region, being at the crossroads of different aerosol species originating from local urban-industrial and biomass-burning activities, regional dust sources, and European pollution from the north. The Environmental Climate Model (EnvClimA) is used to investigate both of the biogenic and anthropogenic aerosols over Egypt. The dominant natural aerosols over Egypt are due to the sand and dust storms, which frequently occur during the transitional seasons (spring and autumn). In winter, the maximum frequency reaches 2 to 3 per day in the north, which decreases gradually southward with a frequency of 0.5-1 per day. Monitoring one of the most basic aerosol parameters, the aerosol optical depth (AOD), is a main experimental and modeling task in aerosol studies. We used the aerosol optical depth to quantify the amount and variability of aerosol loading in the atmospheric column over a certain areas. The aerosols optical depth from the model is higher in spring season due to the impacts of dust activity over Egypt as results of the westerly wind, which carries more dust particles from the Libyan Desert. The model result shows that the mass load of fine aerosols has a longer life-time than the coarse aerosols. In autumn season, the modelled aerosol optical depth tends to increase due to the biomass burning in the delta of Egypt. Natural aerosol from the model tends to scatter the solar radiation while most of the anthropogenic aerosols tend to absorb the longwave solar radiation. The overall results indicate that the AOD is lowest in winter

  10. Examining the role of NOx and acidity on organic aerosol formation through predictions of key isoprene aerosol species in the United States

    EPA Science Inventory

    Isoprene is a significant contributor to organic aerosol in the Southeastern United States. Later generation isoprene products, specifically isoprene epoxydiols (IEPOX) and methacryloylperoxynitrate (MPAN), have been identified as SOA precursors. The contribution of each pathway ...

  11. Composition and spectral characteristics of ambient aerosol at Mauna Loa Observatory

    SciTech Connect

    Johnson, S.A.; Kumar, R. )

    1991-03-20

    Ambient aerosol particles were sampled continuously with a time resolution of {approximately}4 hours for a period of 8 days at the Mauna Loa Observatory, Hawaii, in August 1986. The samples were analyzed on-site for their chemical composition by attenuated total internal reflection infrared spectroscopy. The infrared absorption spectra of the samples also provided data on aerosol light absorbance characteristics at 9.1 and 10.6 {mu}m - wavelengths of interest in determining aerosol backscatter coefficients for CO{sub 2} lidars. The chemical species in the ambient aerosol varied considerably during this 8-day period. The aerosol was acidic ((NH{sub 4}){sub 3}H(SO{sub 4}){sub 2},NH{sub 4}HSO{sub 4}, or H{sub 2}SO{sub 4}) rather than neutral ((NH{sub 4}){sub 2}SO{sub 4}) for a major fraction of the sampling time. The samples generally showed much higher absorbance at 9.1 {mu}m than at 10.6 {mu}m. Changes in the chemical composition between (NH{sub 4}){sub 2}SO{sub 4} and the more acidic forms were accompanied by substantial changes in the sample's absorbance at 9.1 {mu}m but lesser changes in the absorbance at 10.6 {mu}m. These variations could have a profound effect on backscatter coefficients of atmospheric aerosol particles at CO{sub 2} wavelengths.

  12. Charicteristics of Aerosol indices distribution followed by Aerosol types

    NASA Astrophysics Data System (ADS)

    Park, S.; Kim, J.; Lee, J.; Kim, M.; Lee, S.; Song, C.

    2010-12-01

    Transboundary transport of aerosol has been a hot issue in East Asia and with various aerosol types from different source region. To detect signals from aerosols, OMI provides aerosol indices. Aerosol Indices (AI) represent the change of spectral contrast between two wavelengths and these indices are derived in UV and Visible regions. These indices also can get not only in ocean but also in land region so that AI is good to observe the source region and transport of aerosols. In UV region, AI (UV-AI) can classify the absorbing and non-absorbing aerosols (Torres et al., 1998) so that this value is frequently used for dust detection. Additionally, visible AI (VIS-AI) uses to differentiate the absorbing and non-absorbing aerosol types. If we combine two types of indices at the coordinate system of two types of AI, distribution of indices contains different signals if aerosol types change theoretically. In this study, we want to find out classification results based by the observation data to see the theoretical distribution in two AI values. For the observation data, aerosol types are obtained from the results of MODIS-OMI algorithm and 4-channel algorithm classify four types of aerosols, i.e. dust, carbonaceous, sea-salt and Non-Absorbing (NA). These algorithms classify aerosol by using the characteristics of aerosol optical properties in visible and near IR regions. MODIS-OMI algorithm uses the MODIS AOD and UV-AI in OMI values. For UV-AI case, dust and carbonaceous types have larger UV-AI values than non-absorbing aerosols because of absorbing characteristics. However, dust and carbonaceous types cannot classify if UV-AI values use only. For VIS-AI case, dust has larger proportion, but carbonaceous aerosol has smaller proportion in high AI value. However, VIS-AI cannot clearly classify between dust and carbonaceous types except for the case of extremely high AI cases. In NA type, VIS-AI has almost positive values, but the distribution has smaller than the absorbing

  13. Measuring Uptake Coefficients and Henry's Law Constants of Gas-Phase Species with Models for Secondary Organic Aerosol

    NASA Astrophysics Data System (ADS)

    Fairhurst, M. C.; Waring-Kidd, C.; Ezell, M. J.; Finlayson-Pitts, B. J.

    2014-12-01

    Volatile organic compounds (VOC) are oxidized in the atmosphere and their products contribute to secondary organic aerosol (SOA) formation. These particles have been shown to have effects on visibility, climate, and human health. Current models typically under-predict SOA concentrations from field measurements. Underestimation of these concentrations could be a result of how models treat particle growth. It is often assumed that particles grow via instantaneous thermal equilibrium partitioning between liquid particles and gas-phase species. Recent work has shown that growth may be better represented by irreversible, kinetically limited uptake of gas-phase species onto more viscous, tar-like SOA. However, uptake coefficients for these processes are not known. The goal of this project is to measure uptake coefficients and solubilities for different gases onto models serving as proxies for SOA and determine how they vary based on the chemical composition of the gas and the condensed phase. Experiments were conducted using two approaches: attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy and a flow system coupled to a mass spectrometer. The ATR crystal was coated with the SOA proxy and the gas-phase species introduced via a custom flow system. Uptake of the gas-phase species was characterized by measuring the intensity of characteristic IR bands as a function of time, from which a Henry's law constant and initial estimate of uptake coefficients could be obtained. Uptake coefficients were also measured in a flow system where the walls of the flow tube were coated with the SOA proxy and gas-phase species introduced via a moveable inlet. Uptake coefficients were derived from the decay in gas-phase species measured by mass spectrometry. The results of this work will establish a structure-interaction relationship for uptake of gases into SOA that can be implemented into regional and global models.

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

    NASA Astrophysics Data System (ADS)

    Bililign, Solomon; Fiddler, Marc; Singh, Sujeeta

    2012-02-01

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

  15. The optical constants of several atmospheric aerosol species - Ammonium sulfate, aluminum oxide, and sodium chloride

    NASA Technical Reports Server (NTRS)

    Toon, O. B.; Pollack, J. B.; Khare, B. N.

    1976-01-01

    An investigation is conducted of problems which are related to a use of measured optical constants in the simulation of the optical constants of real atmospheric aerosols. The techniques of measuring optical constants are discussed, taking into account transmission measurements through homogeneous and inhomogeneous materials, the immersion of a material in a liquid of a known refractive index, the consideration of the minimum deviation angle of prism measurement, the interference of multiply reflected light, reflectivity measurements, and aspects of mathematical analysis. Graphs show the real and the imaginary part of the refractive index as a function of wavelength for aluminum oxide, NaCl, and ammonium sulfate. Tables are provided for the dispersion parameters and the optical constants.

  16. Analysis of organic and inorganic species on the surface of atmospheric aerosol using time-of-flight secondary ion mass spectrometry (TOF-SIMS)

    NASA Astrophysics Data System (ADS)

    Peterson, Richard E.; Tyler, Bonnie J.

    This work explores the utility of time-of-flight static secondary-ion mass spectrometry (TOF-SIMS) for the analysis of the surface organic layer on individual atmospheric aerosol particles. The surface sensitivity and minimal fragmentation available with TOF-SIMS suggest that it can be a powerful tool for the examination of the organic and inorganic species on the surface of individual particles. Cascade impactors were used to collect aerosol from summer 2000 Montana forest fires, winter snowmobile samples in Yellowstone National Park, Hawaiian lava and sea salt, from an Asian Dust event reaching Salt Lake City, Utah in April 2001 and from Salt Lake Valley summer urban aerosol. TOF-SIMS analysis and multivariate statistical techniques combined gave chemical and morphological information about the particles. Surfaces of the aerosol from forest fires, snowmobile exhaust, and sea salt were all dominated by aliphatic hydrocarbons and their amphiphilic derivatives. Each source showed a different organic chemical signature. The extent and composition of the organics layer which typically covers the surface of atmospheric particles are expected to effect all of the surface related aerosol properties such as health effects, the ability of the particle to activate and form cloud droplets, and the aggregation of particles as well as reactions between the particle and gas phase species.

  17. Statistical analysis of aerosol species, trace gasses, and meteorology in Chicago.

    PubMed

    Binaku, Katrina; O'Brien, Timothy; Schmeling, Martina; Fosco, Tinamarie

    2013-09-01

    Both canonical correlation analysis (CCA) and principal component analysis (PCA) were applied to atmospheric aerosol and trace gas concentrations and meteorological data collected in Chicago during the summer months of 2002, 2003, and 2004. Concentrations of ammonium, calcium, nitrate, sulfate, and oxalate particulate matter, as well as, meteorological parameters temperature, wind speed, wind direction, and humidity were subjected to CCA and PCA. Ozone and nitrogen oxide mixing ratios were also included in the data set. The purpose of statistical analysis was to determine the extent of existing linear relationship(s), or lack thereof, between meteorological parameters and pollutant concentrations in addition to reducing dimensionality of the original data to determine sources of pollutants. In CCA, the first three canonical variate pairs derived were statistically significant at the 0.05 level. Canonical correlation between the first canonical variate pair was 0.821, while correlations of the second and third canonical variate pairs were 0.562 and 0.461, respectively. The first canonical variate pair indicated that increasing temperatures resulted in high ozone mixing ratios, while the second canonical variate pair showed wind speed and humidity's influence on local ammonium concentrations. No new information was uncovered in the third variate pair. Canonical loadings were also interpreted for information regarding relationships between data sets. Four principal components (PCs), expressing 77.0 % of original data variance, were derived in PCA. Interpretation of PCs suggested significant production and/or transport of secondary aerosols in the region (PC1). Furthermore, photochemical production of ozone and wind speed's influence on pollutants were expressed (PC2) along with overall measure of local meteorology (PC3). In summary, CCA and PCA results combined were successful in uncovering linear relationships between meteorology and air pollutants in Chicago and

  18. Characterization of radicals and high-molecular weight species from alpha-pinene/ozone reaction and ambient aerosol samples

    NASA Astrophysics Data System (ADS)

    Pavlovic, Jelica

    Secondary organic aerosol formed during oxidation of different volatile organic compounds is composed from a number of final and intermediate reaction products. The final products include compounds in both low and high molecular weight range called also oligomer species. These compounds can be highly volatile, as well as being semi- or low-volatility compounds. This study characterized intermediate reactive radical products formed from previously often studied alpha-pinene/ozone reaction. In order to passivate those radical species nitrone spin traps were used. 5,5-dimethyl-4,5-dihydro-3H-pyrrole-N-oxide (DMPO), and 5-dietoxyphosphoryl-5-methyl-1-pyrroline-N-oxide (DEPMPO) traps were able to successfully trap oxygen- and carbon-centered radicals produced from alpha-pinene/ozone reaction. Electrospray ionization (ESI) in negative ion mode with mass spectrometry (MS) detection was used to scan spectra of formed spin trap adducts and the tandem mass spectrometry (MSn) to elucidate its structures as well as structures of captured radicals. The same method was applied to analyze radical species present in ambient PM2.5 samples. Few carbon- (alkyl) and oxygen- (alkoxyl) centered radicals were captured with DMPO and DEPMPO traps. The second part of this study was focused on high molecular weight (high-MW) species formed from the same reaction (alpha-pinene/ozone), but found also in fine particulate matter fractions of ambient samples. LC/MS/MS analysis of dimer species from chamber study revealed fragments that can originate from peroxide structures. Proposed reaction for these peroxide dimer formation is self reaction of two peroxyl radicals, followed by the loss of oxygen molecule. These findings emphasize the role of peroxyl (ROO) radicals in formation of high-MW products and are in line with the high O:C ratio results reported in other studies. Water soluble organic carbon (WSOC) extracts of three size fractions of the ambient aerosol, PM1--2.5, PM0.1--1, and PM<0

  19. Speciation of 127I and 129I in atmospheric aerosols at Risø, Denmark: insight into sources of iodine isotopes and their species transformations

    NASA Astrophysics Data System (ADS)

    Zhang, L. Y.; Hou, X. L.; Xu, S.

    2015-09-01

    Speciation analysis of iodine in aerosols is a very useful approach for understanding geochemical cycling of iodine in the atmosphere. In this study, overall iodine species, including water-soluble iodine species (iodide, iodate and water-soluble organic iodine), NaOH-soluble iodine and insoluble iodine have been determined for 129I and 127I in the aerosols collected at Risø, Denmark, between March and May 2011 (shortly after the Fukushima nuclear accident) and in December 2014. The measured concentrations of total iodine are in the range of 1.04-2.48 ng m-3 for 127I and (11.3-97.0) × 105 atoms m-3 for 129I, and 129I / 127I atomic ratios of (17.8-86.8) × 10-8. The contribution of Fukushima-derived 129I (peak value of 6.3 × 104 atoms m-3) is estimated to be negligible (less than 6 %) compared to the total 129I concentration in northern Europe. The concentrations and species of 129I and 127I in the aerosols are found to be strongly related to their sources and atmospheric pathways. Aerosols that were transported over the contaminated ocean, contained higher amounts of 129I than aerosols transported over the European continent. The high 129I concentrations of the marine aerosols are attributed to secondary emission from heavily 129I-contaminated seawater rather than primary gaseous release from nuclear reprocessing plants. Water-soluble iodine was found to be a minor fraction to total iodine for both 127I (7.8-13.7 %) and 129I (6.5-14.1 %) in ocean-derived aerosols, but accounted for 20.2-30.3 % for 127I and 25.6-29.5 % for 129I in land-derived aerosols. Iodide was the predominant form of water-soluble iodine, accounting for more than 97 % of the water-soluble iodine. NaOH-soluble iodine seems to be independent of the sources of aerosols. The significant proportion of 129I and 127I found in NaOH-soluble fractions is likely bound with organic substances. In contrast to water-soluble iodine however, the sources of air masses exerted distinct influences on insoluble

  20. Speciation of 127I and 129I in atmospheric aerosols at Risø, Denmark: insight into sources of iodine isotopes and their species transformations

    NASA Astrophysics Data System (ADS)

    Zhang, Luyuan; Hou, Xiaolin; Xu, Sheng

    2016-02-01

    Speciation analysis of iodine in aerosols is a very useful approach for understanding geochemical cycling of iodine in the atmosphere. In this study, overall iodine species, including water-soluble iodine species (iodide, iodate and water-soluble organic iodine), NaOH-soluble iodine, and insoluble iodine have been determined for 129I and 127I in the aerosols collected at Risø, Denmark, during March and May 2011 (shortly after the Fukushima nuclear accident) and in December 2014. The measured concentrations of total iodine are in the range of 1.04-2.48 ng m-3 for 127I and (11.3-97.0) × 105 atoms m-3 for 129I, corresponding to 129I / 127I atomic ratios of (17.8-86.8) × 10-8. The contribution of Fukushima-derived 129I (peak value of 6.3 × 104 atoms m-3) is estimated to be negligible (less than 6 %) compared to the total 129I concentration in northern Europe. The concentrations and species of 129I and 127I in the aerosols are found to be strongly related to their sources and atmospheric pathways. Aerosols that were transported over the contaminated seas contained higher concentrations of 129I than aerosols transported over the European continent. The high 129I concentrations of the marine aerosols are attributed to secondary emission of marine discharged 129I in the contaminated seawater in the North Sea, North Atlantic Ocean, English Channel, Kattegat, etc., rather than direct gaseous release from the European nuclear reprocessing plants (NRPs). Water-soluble iodine was found to be a minor fraction to the total iodine for both 127I (7.8-13.7 %) and 129I (6.5-14.1 %) in ocean-derived aerosols, but accounted for 20.2-30.3 % for 127I and 25.6-29.5 % for 129I in land-derived aerosols. Iodide was the predominant form of water-soluble iodine, accounting for more than 97 % of the water-soluble iodine. NaOH-soluble iodine seems to be independent of the sources of aerosols. The significant proportion of 129I and 127I found in NaOH-soluble fractions is likely bound with

  1. Tropospheric Aerosols

    NASA Astrophysics Data System (ADS)

    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

  2. Aerosol Angstrom Absorption Coefficient Comparisons during MILAGRO.

    NASA Astrophysics Data System (ADS)

    Marley, N. A.; Marchany-Rivera, A.; Kelley, K. L.; Mangu, A.; Gaffney, J. S.

    2007-12-01

    Measurements of aerosol absorption were obtained as part of the MAX-Mex component of the MILAGRO field campaign at site T0 (Instituto Mexicano de Petroleo in Mexico City) by using a 7-channel aethalometer (Thermo- Anderson) during the month of March, 2006. The absorption measurements obtained in the field at 370, 470, 520, 590, 660, 880, and 950 nm were used to determine the aerosol Angstrom absorption exponents by linear regression. Since, unlike other absorbing aerosol species (e.g. humic like substances, nitrated PAHs), black carbon absorption is relatively constant from the ultraviolet to the infrared with an Angstrom absorption exponent of -1 (1), a comparison of the Angstrom exponents can indicate the presence of aerosol components with an enhanced UV absorption over that expected from BC content alone. The Angstrom exponents determined from the aerosol absorption measurements obtained in the field varied from - 0.7 to - 1.3 during the study and was generally lower in the afternoon than the morning hours, indicating an increase in secondary aerosol formation and photochemically generated UV absorbing species in the afternoon. Twelve-hour integrated samples of fine atmospheric aerosols (<0.1micron) were also collected at site T0 and T1 (Universidad Technologica de Tecamac, State of Mexico) from 5 am to 5 pm (day) and from 5 pm to 5 am (night) during the month of March 2006. Samples were collected on quartz fiber filters with high volume impactor samplers. Continuous absorption spectra of these aerosol samples have been obtained in the laboratory from 280 to 900nm with the use of an integrating sphere coupled to a UV spectrometer (Beckman DU with a Labsphere accessory). The integrating sphere allows the detector to collect and spatially integrate the total radiant flux reflected from the sample and therefore allows for the measurement of absorption on highly reflective or diffusely scattering samples. These continuous spectra have also been used to obtain the

  3. Reactions of SIV species with organic compounds: formation mechanisms of organo-sulfur derivatives in atmospheric aerosols

    NASA Astrophysics Data System (ADS)

    Passananti, Monica; Shang, Jing; Dupart, Yoan; Perrier, Sébastien; George, Christian

    2015-04-01

    Secondary organic aerosol (SOA) have an important impact on climate, air quality and human health. However the chemical reactions involved in their formation and growth are not fully understood or well-constrained in climate models. It is well known that inorganic sulfur (mainly in oxidation states (+IV) and (+VI)) plays a key role in aerosol formation, for instance sulfuric acid is known to be a good nucleating gas. In addition, acid-catalyzed heterogeneous reactions of organic compounds has shown to produce new particles, with a clear enhancement in the presence of ozone (Iinuma 2013). Organosulfates have been detected in tropospheric particles and aqueous phases, which suggests they are products of secondary organic aerosol formation process (Tolocka 2012). Originally, the production of organosulfates was explained by the esterification reaction of alcohols, but this reaction in atmosphere is kinetically negligible. Other formation pathways have been suggested such as hydrolysis of peroxides and reaction of organic matter with sulfite and sulfate radical anions (SO3-, SO4-) (Nozière 2010), but it remains unclear if these can completely explain atmospheric organo-sulfur aerosol loading. To better understand the formation of organo-sulfur compounds, we started to investigate the reactivity of SIV species (SO2 and SO32-) with respect to specific functional groups (organic acids and double bonds) on atmospherically relevant carboxylic acids and alkenes. The experiments were carried out in the homogeneous aqueous phase and at the solid-gas interface. A custom built coated-wall flow tube reactor was developed to control relativity humidity, SO2 concentration, temperature and gas flow rate. Homogeneous and heterogeneous reaction kinetics were measured and resulting products were identified using liquid chromatography coupled with an orbitrap mass spectrometer (LC-HR-MS). The experiments were performed with and without the presence of ozone in order to evaluate any

  4. Identification of nitrogenous organic species in Titan aerosols analogs: Nitrogen fixation routes in early atmospheres

    NASA Astrophysics Data System (ADS)

    He, Chao; Smith, Mark A.

    2013-09-01

    Titan, an icy world surrounded by auburn organic haze, is considered as one of the best targets for studying abiotic planetary organic chemistry. In spite of a great many efforts being made, the chemistry in Titan’s atmosphere and its resulting chemical structures are still not fully understood. In our previous work, we have investigated the structure of Titan aerosols analogs (tholin) by NMR and identified hexamethylenetetramine as a dominant small molecule in Titan tholin. Here we report a more complete and definitive structural investigation of the small molecule inventory in Titan tholin. We identified several nitrogenous organic molecules including cyanamide, guanidine, 2-cyanoguanidine, melamine, N‧-cyanoformamidine and 1,2,4-triazole in Titan tholin by using NMR and GC-MS and standard sample comparison. The structural characteristics of these molecules suggest a possible formation pathway from the reaction of HCN and NH3, both of which are known to exist in appreciable density in the atmosphere and were tentatively detected by the Huygens probe.

  5. Real-time measurements of ammonia, acidic trace gases and water-soluble inorganic aerosol species at a rural site in the Amazon Basin

    NASA Astrophysics Data System (ADS)

    Trebs, I.; Meixner, F. X.; Slanina, J.; Otjes, R.; Jongejan, P.; Andreae, M. O.

    2004-06-01

    We measured the mixing ratios of ammonia (NH3), nitric acid (HNO3), nitrous acid (HONO), hydrochloric acid (HCl), sulfur dioxide (SO2 and the corresponding water-soluble inorganic aerosol species, ammonium (NH4+), nitrate (NO3-), nitrite (NO2-), chloride (Cl- and sulfate (SO42-), and their diel and seasonal variations at a pasture site in the Amazon Basin (Rondônia, Brazil). This study was conducted within the framework of LBA-SMOCC (Large Scale Biosphere Atmosphere Experiment in Amazonia - Smoke Aerosols, Clouds, Rainfall and Climate: Aerosols from Biomass Burning Perturb Global and Regional Climate). Sampling was performed from 12 September to 14 November 2002, extending from the dry season (extensive biomass burning activity), through the transition period to the wet season (background conditions). Measurements were made continuously using a wet-annular denuder (WAD) in combination with a Steam-Jet Aerosol Collector (SJAC) followed by suitable on-line analysis. A detailed description and verification of the inlet system for simultaneous sampling of soluble gases and aerosol compounds is presented. Overall measurement uncertainties of the ambient mixing ratios usually remained below 15%. The limit of detection (LOD) was determined for each single data point measured during the field experiment. Median LOD values (3σ-definition) were ≤0.015ppb for acidic trace gases and aerosol anions and ≤0.118ppb for NH3 and aerosol NH4+. Mixing ratios of acidic trace gases remained below 1ppb throughout the measurement period, while NH3 levels were an order of magnitude higher. Accordingly, mixing ratios of NH4+ exceeded those of other inorganic aerosol contributors by a factor of 4 to 10. During the wet season, mixing ratios decreased by nearly a factor of 3 for all compounds compared to those observed when intensive biomass burning took place. Additionally, N-containing gas and aerosol species featured pronounced diel variations. This is attributed to strong relative

  6. Aerosol species concentrations and source apportionment of ammonia at Rocky Mountain National Park.

    PubMed

    Malm, William C; Schichtel, Bret A; Barna, Michael G; Gebhart, Kristi A; Rodriguez, Marco A; Collett, Jeffrey L; Carrico, Christian M; Benedict, Katherine B; Prenni, Anthony J; Kreidenweis, Sonia M

    2013-11-01

    Changes in ecosystem function at Rocky Mountain National Park (RMNP) are occurring because of emissions of nitrogen and sulfate species along the Front Range of the Colorado Rocky Mountains, as well as sources farther east and west. The nitrogen compounds include both oxidized and reduced nitrogen. A year-long monitoring program of various oxidized and reduced nitrogen species was initiated to better understand their origins as well as the complex chemistry occurring during transport from source to receptor. Specifically the goals of the study were to characterize the atmospheric concentrations of nitrogen species in gaseous, particulate, and aqueous phases (precipitation and clouds) along the east and west sides of the Continental Divide; identify the relative contributions to atmospheric nitrogen species in RMNP from within and outside of the state of Colorado; identify the relative contributions to atmospheric nitrogen species in RMNP from emission sources along the Colorado Front Range versus other areas within Colorado; and identify the relative contributions to atmospheric nitrogen species from mobile sources, agricultural activities, and large and small point sources within the state of Colorado. Measured ammonia concentrations are combined with modeled releases of conservative tracers from ammonia source regions around the United States to apportion ammonia to its respective sources, using receptor modeling tools.

  7. Airborne Fungi in Sahara Dust Aerosols Reaching the Eastern Caribbean: II. Species Identification Using Molecular Techniques

    NASA Astrophysics Data System (ADS)

    de La Mota, A.; Betancourt, C.; Detres, Y.; Armstrong, R.

    2003-12-01

    Fungi samples from filters collected in Castle Bruce, Dominica from March through July 2002, were previously purified and identified to genus level using classic macroscopic and microscopic techniques. A total of 105 isolated colonies were cultured in liquid media and the mycelial mats used for DNA extraction. PCR was used to amplify the ITS region of the rDNA using the ITS1 and ITS4 primers. Both strands of the amplified products were sequenced and the final identification to species level was completed by a GenBank search. Fourteen different species and one fungal endophyte were identified from genders Aspergillus,Penicillium, Fusarium, Cladosporium, Curvularia and Phanerochaete. Some of these species such as A. fumigatus, A. japonicus, P. citrinum and C. cladosporoides are known to cause respiratory disorders in humans. A. fumigatus causes an aggressive pulmonary allergic response that might result in allergic bronchopulmonary aspergillosis. Other species such as F. equiseti and C. brachyspora are plant pathogens affecting economically important crops. Sahara dust is an important source of fungal spores of species that are not common in the Caribbean region.

  8. Vertical distribution of non-volatile species of upper tropospheric and lower stratospheric aerosol observed by balloon-borne optical particle counter above Ny-Aalesund, Norway in the winter of 2015

    NASA Astrophysics Data System (ADS)

    Shiraishi, K.; Hayashi, M.; Shibata, T.; Neuber, R.; Ruhe, W.

    2015-12-01

    The polar lower stratosphere is the sink area of stratospheric global circulation. The composition, concentration and size distribution of aerosol in the polar stratosphere are considered to be strongly influenced by the transportations from mid-latitude to polar region and exchange of stratosphere to troposphere. In order to study the aerosol composition and size distribution in the Arctic stratosphere and the relationship between their aerosol microphysical properties and transport process, we carried out balloon-borne measurement of aerosol volatility above Ny-Aalesund, Norway in the winter of 2015. In our observation, two optical particle counters and a thermo denuder were suspended by one rubber balloon. A particle counter measured the heated aerosol size distribution (after heating at the temperature of 300 degree by the thermo denuder) and the other measured the ambient aerosol size distribution during the observation. The observation was carried out on 15 January, 2015. Balloon arrived at the height of 30km and detailed information of aerosol size distributions in upper troposphere and lower stratosphere for both heated aerosol and ambient aerosol were obtained. As a Result, the number ratio of non-volatile particles to ambient aerosol particles in lower stratosphere (11-15km) showed different feature in particle size range of fine mode (0.3aerosol particles were 1-3% in fine mode range and 7-20% in coarse mode range. They suggested that fine particles are composed dominantly of volatile species (probably sulfuric acid), and coarse particles are composed of non-volatile species such as minerals, sea-salts. In our presentation, we show the obtained aerosol size distribution and discuss the aerosol compositions and their transport process.

  9. Real-time measurements of ammonia, acidic trace gases and water-soluble inorganic aerosol species at a rural site in the Amazon Basin

    NASA Astrophysics Data System (ADS)

    Trebs, I.; Meixner, F. X.; Slanina, J.; Otjes, R.; Jongejan, P.; Andreae, M. O.

    2004-02-01

    We measured the mixing ratios of ammonia (NH3), nitric acid (HNO3), nitrous acid (HONO), hydrochloric acid (HCl), sulfur dioxide (SO2) and the corresponding water-soluble inorganic aerosol species, ammonium (NH4+), nitrate (NO3-), nitrite (NO2-), chloride (Cl-) and sulfate (SO42-), and their diel and seasonal variations at a pasture site in the Amazon Basin (Rondônia, Brazil). This study was conducted within the framework of LBA-SMOCC (Large Scale Biosphere Atmosphere Experiment in Amazonia Smoke Aerosols, Clouds, Rainfall and Climate). Sampling was performed from 12 September to 14 November 2002, extending from the dry season (extensive biomass burning activity), through the transition period to the wet season (background conditions). Measurements were made continuously using a wet-annular denuder in combination with a Steam-Jet Aerosol Collector (SJAC) followed by suitable on-line analysis. A detailed description and verification of the inlet system for simultaneous sampling of soluble gases and aerosol compounds is presented. Overall measurement uncertainties of the ambient mixing ratios usually remained below 15%. The limit of detection (LOD) was determined for each single data point measured during the field experiment. Median LOD values (3σ-definition) were ≤0.015 ppb for acidic trace gases and aerosol anions and ≤0.118 ppb for NH3 and aerosol NH4+. Mixing ratios of acidic trace gases remained below 1ppb throughout the measurement period, while NH3 levels were an order of magnitude higher. Accordingly, mixing ratios of NH4+ exceeded those of other inorganic aerosol contributors by a factor of 4 to 10. During the wet season, mixing ratios decreased by nearly a factor of 3 for all compounds compared to those observed when intensive biomass burning took place. Additionally, N-containing gas and aerosol species featured pronounced diel variations. This is attributed to strong relative humidity and temperature variations between day and night as well as to

  10. Analysis of inorganic mercury species associated with airborne particulate matter/aerosols: method development.

    PubMed

    Feng, Xinbin; Lu, Julia Y; Grègoire, D Conrad; Hao, Yingjie; Banic, Catharine M; Schroeder, William H

    2004-10-01

    This paper describes a method for speciation of Hg associated with airborne particulate matter. This method uses a mini-sampler for sample collection and analysis, thermal desorption for separating Hg species, and inductively coupled plasma mass spectrometry (ICP-MS) for identification and quantification of Hg. Coal fly ash spiked with different Hg compounds (e.g. Hg0, HgCl2, HgO, and HgS) was used for qualitative calibration. A standard reference material with a certified value for Hg concentration was used to evaluate the method. When the temperature of the furnace was programmed at a linear rate of increase of 50 degrees min(-1), different Hg compounds could clearly be separated. Three airborne particulate matter samples were collected in parallel in Toronto, ON, Canada and analyzed using this method. Reproducible results were obtained and Hg0, HgCl2, HgO, and HgS species from these samples were detected.

  11. Rare Isotope Insights into Supereruptions: Rare Sulfur and Triple Oxygen Isotope Geochemistry of Stratospheric Sulfate Aerosols Absorbed on Volcanic Ash Particles

    NASA Astrophysics Data System (ADS)

    Bindeman, I. N.; Eiler, J.; Wing, B.; Farquhar, J.

    2006-12-01

    We present analyses of stable isotopic ratios of 17O/16O, 18O/16O, 34S/32S, and 33S/32S, 36S/32S of sulfate leached from volcanic ash of a series of well-known volcanic eruptions. This list covers much of the diversity of sizes and the character of volcanic eruptions. Particular emphasis is paid to the Lava Creek Tuff of Yellowstone and we present wide geographic sample coverage for this unit. This global dataset spans a significant range in δ34S, δ18O, and Δ17O of sulfate (29, 30 and 3.3 permil respectively) with oxygen isotopes recording mass-independent fractionation and sulfur isotopes exhibiting mass-dependent behavior. These ranges are defined by the isotopic compositions of products of large caldera forming eruptions. Proximal ignimbrites and coarse ash typically do not contain sulfate. The presence of sulfate with Δ17O > 0.2 permil is characteristic of small distal ash particles, suggesting that sulfate aerosols were scavenged after they underwent atmospheric photochemical reactions. Additionally, sediments that embed ash layers either do not contain sulfate or contain minor sulfate with Δ17O near 0 permil, suggesting that the observed sulfate in ash is of volcanic origin. Mass-dependent sulfur isotopic compositions suggest that sulfate-forming reactions did not involve photolysis of SO2, unlike the situation inferred for some pre-2.3 Ga sulfates or hypothesized to occur during the formation of sulfate associated with plinian eruptions that pierce the ozone layer. However, sulfate in the products of caldera-forming eruptions display a large δ34S range and fractionation relationships that do not follow equilibrium slopes of 0.515 and 1.90 for 33S/32S vs. 34S/32S and 36S/32S vs. 34S/32S, respectively. This implies that the sulfur isotopic characteristics of these sulfates were not set by a single stage, high-temperature equilibrium process in the volcanic plum. The data presented here are consistent with a single stage kinetic fractionation of sulfur

  12. Toward Investigating Optically Trapped Organic Aerosols with CARS Microspectroscopy

    NASA Astrophysics Data System (ADS)

    Voss, L. F.

    2009-12-01

    The Intergovernmental Panel on Climate Change notes the huge uncertainty in the effect that atmospheric aerosols play in determining overall global temperature, specifically in their ability to nucleate clouds. To better understand aerosol chemistry, the novel coupling of gradient force optical trapping with broad bandwidth coherent anti-Stokes Raman scattering (CARS) spectroscopy is being developed to study single particles suspended in air. Building on successful designs employed separately for the techniques, this hybrid technology will be used to explain how the oxidation of organic compounds changes the chemical and physical properties of aerosols. By trapping the particles, an individual aerosol can be studied for up to several days. Using a broad bandwidth pulse for one of the incident beams will result in a Raman vibrational spectrum from every laser pulse. Combined with signal enhancement due to resonance and coherence of nonlinear CARS spectroscopy, this technique will allow for acquisition of data on the millisecond time scale, facilitating the study of dynamic processes. This will provide insights on how aerosols react with and absorb species from the gas phase. These experiments will increase understanding of aerosol oxidation and growth mechanisms and the effects that aerosols have on our atmosphere and climate. Progress in efforts developing this novel technique to study model systems is presented.

  13. An Investigation of Aerosol Measurements from the Halogen Occultation Experiment: Validation, Size Distributions, Composition, and Relation to Other Chemical Species

    NASA Technical Reports Server (NTRS)

    Deshler, Terry; Hervig, Mark E.

    1998-01-01

    The efforts envisioned within the original proposal (accepted February 1994) and the extension of this proposal (accepted February 1997) included measurement validations, the retrieval of aerosol size distributions and distribution moments, aerosol correction studies, and investigations of polar stratospheric clouds. A majority of the results from this grant have been published. The principal results from this grant are discussed.

  14. Sound Absorbers

    NASA Astrophysics Data System (ADS)

    Fuchs, H. V.; Möser, M.

    Sound absorption indicates the transformation of sound energy into heat. It is, for instance, employed to design the acoustics in rooms. The noise emitted by machinery and plants shall be reduced before arriving at a workplace; auditoria such as lecture rooms or concert halls require a certain reverberation time. Such design goals are realised by installing absorbing components at the walls with well-defined absorption characteristics, which are adjusted for corresponding demands. Sound absorbers also play an important role in acoustic capsules, ducts and screens to avoid sound immission from noise intensive environments into the neighbourhood.

  15. Aerosol radiative effects on the meteorology and distribution of pollutants in the Mexico City Metropolitan Area during MCMA-2006/MILAGRO Campaign

    NASA Astrophysics Data System (ADS)

    Li, Guohui; Bei, Naifang; Molina, Luisa

    2013-04-01

    Aerosols scatter or absorb incoming solar radiation, perturb the temperature structure of the atmosphere, and impact meteorological fields and further the distribution of gas phase species and aerosols. In the present study, the aerosol radiative effects on the meteorology and photochemistry in the Mexico City Metropolitan Area (MCMA) are investigated using the WRF-CHEM model during the period from March 24th to 29th associated with the MILAGRO-2006 campaign. Aerosols decrease incoming solar radiation by up to 20% and reduce the surface temperature by up to 0.5 °C due to scattering and absorbing the incoming solar radiation in Mexico City. The absorption of black carbon aerosols can also enhance slightly the temperature in the planetary boundary layer (PBL). Generally, the change of the PBL height in the city is less than 200 m during daytime due to the aerosol-induced perturbation of temperature profile. Wind fields are also adjusted with the variation of temperatures, but all the aerosol-induced meteorological changes cannot significantly influence the distribution of pollutants in the city. In addition, when convective events occur in the city, the aerosol radiative effects reduce the convective available potential energy (CAPE) and the convective precipitation is generally decreased. Further studies still need to be performed to evaluate the aerosol indirect effect on precipitation in Mexico City.

  16. The Amazon tall tower observatory (ATTO) site - Multi-year aerosol observations and scientific key questions

    NASA Astrophysics Data System (ADS)

    Pöhlker, C.; Barbosa, H. M.; Brito, J.; Carbone, S.; Chi, X.; Kesselmeier, J.; Ditas, F.; Pöhlker, M. L.; Manzi, A. O.; Moran, D.; Poeschl, U.; Ruckteschler, N.; Saturno, J.; Soergel, M.; Su, H.; Walter, D.; Wang, Q.; Wang, Z.; Weber, B.; Wolff, S.; Yanez-Serrano, A. M.; Artaxo, P.; Andreae, M. O.

    2015-12-01

    The Amazon tall tower observatory site is located 150 km NE of Manaus in undisturbed rain forest areas. It serves as a remote measurement station in the Amazon forest with continuous aerosol, trace gas, micrometeorological, and ecological measurements. During part of the rainy season, the atmospheric state approximates pre-industrial conditions, in strong contrast to the dry season, which is dominated by significant pollution from deforestation fires and urban emissions. This presentation will focus on aerosol studies of the past three years. It aims to provide a brief overview of the characteristic seasonality of the aerosol burden at the ATTO site. Moreover, it will discuss the following key questions and current results of the ongoing observations: (i) During the wet season and in the absence of long-range advection of African aerosols, atmospheric conditions at the ATTO site approximate a pristine state, which reveals the genuine contribution of biogenic aerosols. Biogenic particles in the super- and submicron range have been observed and their properties as well as potential sources will be discussed. (ii) In contrast to the classical new particle formation, the occurrence of ultrafine particles is comparably sparse and mainly occurs as short 'bursts', indicating a rather localized character. Our current understanding of this phenomenon and its significance for the overall aerosol burden will be addressed. (iii) Aerosol absorptivity is mainly caused by black carbon, however, indications for the presence of other light absorbing aerosol species have been found. Current results on light absorbing aerosol under clean and polluted conditions will be presented. (iv) Aerosol particles at the ATTO site are typically strongly aged and comprise pronounced internal mixtures, with important implications for their properties. Microspectroscopic analysis helps to obtain insights into atmospheric processing and its impact on particle morphology and phase state.

  17. 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

    NASA Astrophysics Data System (ADS)

    Takahashi, Y.; Furukawa, T.; Kanai, Y.; Uematsu, M.; Zheng, G.; Marcus, M. A.

    2013-03-01

    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 the high

  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

    NASA Astrophysics Data System (ADS)

    Takahashi, Y.; Furukawa, T.; Kanai, Y.; Uematsu, M.; Zheng, G.; Marcus, M. A.

    2013-08-01

    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 mineral

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

    NASA Astrophysics Data System (ADS)

    Srivastava, R.; Ramachandran, S.

    2012-12-01

    Aerosols are a major atmospheric variable which perturb the Earth-atmosphere radiation balance by absorbing and scattering the solar and terrestrial radiation. Aerosols are produced by natural and anthropogenic processes. The presence of different types of aerosol over a location and aerosols transported from long-range can give rise to different mixing states because of aging and interaction among the different aerosol species. Knowledge of the mixing state of aerosols is important for an accurate assessment of aerosols in climate forcing, as assumptions regarding the mixing state of aerosol and its effect on optical properties can give rise to uncertainties in modeling their direct and indirect effects [1]. Seasonal variations in mixing states of aerosols over an urban (Kanpur) and a rural location (Gandhi College) in the Indo-Gangetic Plain (IGP) are determined using the measured and modeled aerosol optical properties, and the impact of aerosol mixing state on aerosol radiative forcing are investigated. IGP is one of the most populated and polluted river basins in the world, rich in fertile lands and agricultural production. Kanpur is an urban, industrial and densely populated city, and has several large/small scale industries and vehicles, while Gandhi College in IGP is a rural village, located southeast of Kanpur. Aerosol optical properties obtained from Aerosol Robotic Network sun/sky radiometers [2] over these two environmentally distinct locations in Indo-Gangetic Plain are used in the study, along with aerosol vertical profiles obtained from CALIPSO (Cloud- Aerosol Lidar and Infrared Pathfinder Satellite Observations) lidar observations. Probable mixing state of aerosols is determined utilizing the aerosol optical properties viz., aerosol optical depth, single scattering albedo and asymmetry parameter. The coated-sphere Mie calculation requires the refractive index of core and shell species, and the radius of core and shell particles. Core to shell radius

  20. Remote sensing of ocean color and aerosol properties: resolving the issue of aerosol absorption.

    PubMed

    Gordon, H R; Du, T; Zhang, T

    1997-11-20

    Current atmospheric correction and aerosol retrieval algorithms for ocean color sensors use measurements of the top-of-the-atmosphere reflectance in the near infrared, where the contribution from the ocean is known for case 1 waters, to assess the aerosol optical properties. Such measurements are incapable of distinguishing between weakly and strongly absorbing aerosols, and the atmospheric correction and aerosol retrieval algorithms fail if the incorrect absorption properties of the aerosol are assumed. We present an algorithm that appears promising for the retrieval of in-water biophysical properties and aerosol optical properties in atmospheres containing both weakly and strongly absorbing aerosols. By using the entire spectrum available to most ocean color instruments (412-865 nm), we simultaneously recover the ocean's bio-optical properties and a set of aerosol models that best describes the aerosol optical properties. The algorithm is applied to simulated situations that are likely to occur off the U.S. East Coast in summer when the aerosols could be of the locally generated weakly absorbing Maritime type or of the pollution-generated strongly absorbing urban-type transported over the ocean by the winds. The simulations show that the algorithm behaves well in an atmosphere with either weakly or strongly absorbing aerosol. The algorithm successfully identifies absorbing aerosols and provides close values for the aerosol optical thickness. It also provides excellent retrievals of the ocean bio-optical properties. The algorithm uses a bio-optical model of case 1 waters and a set of aerosol models for its operation. The relevant parameters of both the ocean and atmosphere are systematically varied to find the best (in a rms sense) fit to the measured top-of-the-atmosphere spectral reflectance. Examples are provided that show the algorithm's performance in the presence of errors, e.g., error in the contribution from whitecaps and error in radiometric calibration.

  1. Some environmental considerations relating to the interaction of the solid rocket motor exhaust with the atmosphere: Predicted chemical composition of exhaust species and predicted conditions for the formation of HCl aerosol

    NASA Technical Reports Server (NTRS)

    Rhein, R. A.

    1973-01-01

    The exhaust products of a solid rocket motor using as propellant 14% binder, 16% aluminum, and 70% (wt) ammonium perchlorate consist of hydrogen chloride, water, alumina, and other compounds. The equilibrium and some frozen compositions of the chemical species upon interaction with the atmosphere were computed. The conditions under which hydrogen chloride interacts with the water vapor in humid air to form an aerosol containing hydrochloric acid were computed for various weight ratios of air/exhaust products. These computations were also performed for the case of a combined SRM and hydrogen-oxygen rocket engine. Regimes of temperature and relative humidity where this aerosol is expected were identified. Within these regimes, the concentration of HCL in the aerosol and weight fraction of aerosol to gas phase were plotted. Hydrochloric acid aerosol formation was found to be particularly likely in cool humid weather.

  2. Characterization and quantification of aerosol chemical species present below and within cloud over an eastern Himalayan high altitude hill station in India

    NASA Astrophysics Data System (ADS)

    Roy, Arindam; Chatterjee, Abhijit; Sarkar, Chirantan; Ghosh, Sanjay; Raha, Sibaji

    2016-07-01

    There are two main processes through which aerosols and gases get scavenged by rain called below-cloud scavenging or "washout" and in-cloud scavenging or "rainout". The first process refers to the washout of the aerosols and gases present below the cloud during precipitation events by raindrops along their fall. The second process corresponds to the condensation of water vapor on aerosol particles during the formation of cloud droplets and incorporation of gases surrounding the droplets by aqueous-phase reactions. However, the most efficient pathway to remove the atmospheric pollutants is below cloud scavenging which is a major pointer of ecosystem, biogeochemical cycle as well as the climate change. A study has been conducted in 2014 and 2015 monsoon (June-September) in Darjeeling (27.01 ° N, 88.15 ° E), a high altitude (2200 m asl) hill station over eastern Himalaya in India. The study was focused on the below-cloud and in-cloud scavenging of various aerosol ionic species. Attempt was also made to estimate the contribution of in-cloud scavenging and below-cloud scavenging by collecting rain samples sequentially for different rain events. Sea-salt (Na+, sea-Mg2+, Cl- and sea-SO4 2-) and soil dust (non-sea Ca2+, non-sea-Mg2+) species show sharp decrease in concentration for each of the rain sample. This indicates that these species were mostly accumulated below the cloud and washed out during rain. Their concentrations were thus decreased sharply as rains progressed. On the other hand, non-SO4-2 and NH4+ showed different behavior. Their concentrations decreased sharply at the initial stage of the rain and then remained almost constant with rainfall. This explains wash out of these two species at the initial stage of the rain and their contribution from "within the cloud". NH4 + and non-sea-SO4 2- could thus act as cloud condensation nuclei over this part of Himalaya. A strong correlation between these two species indicates their association as (NH4)2SO4. Acidity

  3. Real-time measurement of aerosol black carbon during the Carbonaceous Species Methods Comparison Study, Citrus College, Glendora, California, August 12-21, 1986: Final report

    SciTech Connect

    Hansen, A.D.A.; Novakov, T.

    1987-11-01

    During the period August 12-21, 1986, the Atmospheric Aerosol Research Group of Lawrence Berkeley Laboratory participated in the Carbonaceous Species Method Comparison Study (CSMCS) conducted at Citrus College, Glendora, California. The equipment that we used was the aethalometer, an instrument developed at LBL that measures the concentration of aerosol black carbon in real time. In this report we present our results from that study in the form of 1-minute, 1-hour, and multi-hour average concentrations. We found concentrations generally ranging from 2 to 5 ..mu..g (BC)m/sup 3/, usually with increases in the morning traffic hours. We also observed short-duration (2-15 min) peaks in the black carbon concentration that could be directly attributed to the activity of vehicles in a delivery area less than 50 m from the study site. We conclude that mobile sources were the major contributor to the short- and medium-term variability of aerosol black carbon measured at this site. 5 refs., 5 figs., 1 tab

  4. Quantification of aerosol type, and sources of aerosols over the Indo-Gangetic Plain

    NASA Astrophysics Data System (ADS)

    Kedia, Sumita; Ramachandran, S.; Holben, B. N.; Tripathi, S. N.

    2014-12-01

    Differences and similarities in aerosol characteristics, for the first time, over two environmentally distinct locations in Indo-Gangetic plain (IGP) - Kanpur (KPR) (urban location) and Gandhi College (GC) (rural site) are examined. Aerosol optical depths (AODs) exhibit pronounced seasonal variability with higher values during winter and premonsoon. Aerosol fine mode fraction (FMF) and Ångström exponent (α) are higher over GC than KPR indicating relatively higher fine mode aerosol concentration over GC. Higher FMF over GC is attributed to local biomass burning activities. Analysis of AOD spectra revealed that aerosol size distribution is dominated by wide range of fine mode fractions or mixture of modes during winter and postmonsoon, while during premonsoon and monsoon coarse mode aerosols are more abundant. Single scattering albedo (SSA) is lower over GC than KPR. SSA spectra reveals the abundance of fine mode (coarse mode) absorbing (scattering) aerosols during winter and postmonsoon (premonsoon and monsoon). Spectral SSA features reveal that OC contribution to enhanced absorption is negligible. Analysis shows that absorbing aerosols can be classified as Mostly Black Carbon (BC), and Mixed BC and Dust over IGP. Mixed BC and dust is always higher over KPR, while Mostly BC is higher over GC throughout the year. The amount of long range transported dust exhibits a gradient between KPR (higher) and GC (lower). Results on seasonally varying aerosol types, and absorbing aerosol types and their gradients over an aerosol hotspot are important to tune models and to reduce the uncertainty in radiative and climate impact of aerosols.

  5. Linking Aerosol Source Activities to Present and Future Climate Effects

    NASA Astrophysics Data System (ADS)

    Koch, D.; Bond, T. C.; Streets, D.; Menon, S.; Unger, N.

    2007-05-01

    Aerosol source sectors (transport, power, industry, residential, biomass burning) generate distinct mixtures of aerosol species. These mixtures in turn have different effects on climate. As sectoral emissions change in coming decades, whether by regulation or not, it is helpful to link pollution from source types to climate consequences. We do so, using our global (GISS GCM) aerosol model for present and future IPCC SRES scenarios. According to our model, residential and transport sectors have net positive 1995 aerosol forcings (0.04 and 0.03 W m-2) due to their large black carbon contents. However, the sulfate-dominated power and industry sectors have net negative 1995 forcings (-0.10 and -0.09 W m-2). Due to the near-balance of absorbing and scattering components, biomass burning forcing is small. For the 2050 SRES A1B scenario, the net (negative) aerosol forcing is double 1995 due primarily to increased sulfur emissions in the industry and power sectors. For 2050 B1 the net (negative) forcing decreases relative to 1995, as sulfur emissions are reduced. Both future scenarios project decreasing residential emissions. Yet transport emissions are expected to remain significant and thus become the dominant source of warming aerosols in the future. Aerosol pollution is projected to shift southward relative to the present, as the current industrialized regions generally reduce emissions and tropical and southern hemispheric regions continue to develop. Similar to these SRES scenarios, IIASA scenarios project a decline in residential emissions; however IIASA is more optimistic about transport sector emissions reductions. We will conduct present-day climate experiments, including aerosol direct and indirect effects, to study impacts of power and transport sectors on climate features such as air temperature and hydrologic cycle.

  6. Biomass burning as an important source of reactive oxygen species associated with the atmospheric aerosols in Southeastern United States - Implications for health effects of ambient particulate matter

    NASA Astrophysics Data System (ADS)

    Verma, V.; Weber, R. J. J.; Fang, T.; Xu, L.; Ng, N. L.; Russell, A. G.

    2014-12-01

    We assessed the potential of water-soluble fraction of atmospheric fine aerosols in the southeastern US to generate reactive oxygen species (ROS). ROS-generation potential of particles was quantified by the dithiothreitol (DTT) assay and involved analysis of fine particulate matter (PM) extracted from high-volume quartz filters (23 h integrated daily samples) collected for one year at various sites in different environmental settings in the southeast, including three urban Atlanta sites, and one rural site in Yorkville. Water-soluble PM extracts were further separated into the hydrophobic and hydrophilic fractions using a C-18 column, and both fractions were analyzed for the DTT activity. Organic aerosol (OA) composition was measured at selected sites using a High-Resolution Time-of-Flight Aerosol Mass Spectrophotometer (HR-ToF-AMS). The various factors of the organic aerosols, i.e. Isoprene OA (Isop-OA), hydrocarbon-like OA (HOA), less-oxidized oxygenated OA, (LO-OOA), more-oxidized OOA (MO-OOA), cooking OA (COA), and biomass burning OA (BBOA) were also resolved, and their ability to generate ROS investigated by linear regression techniques. Among all OA factors, BBOA was most consistently associated with ROS, with the highest intrinsic DTT activity of 151±20 pmol/min/μg. The water-soluble bioavailable fraction of BBOA-DTT activity is 2-3 times higher than the reported total-DTT activity of diesel exhaust particles. The total contribution of various aerosol sources to the ROS generating potential was also determined by the positive matrix factorization approach. Interestingly, biomass burning appears as the strongest source of ROS generation, with its annual contribution of 35 % to DTT activity; the contribution was higher in winter (47 %), than summer (24 %) and fall (17 %) seasons. The good agreement between the hydrophobic DTT activity with that estimated from the summed OA components, indicates that humic-like substances (HULIS), which are abundantly emitted

  7. Impact of interannual variations in sources of insoluble aerosol species on orographic precipitation over California's central Sierra Nevada

    NASA Astrophysics Data System (ADS)

    Creamean, J. M.; Ault, A. P.; White, A. B.; Neiman, P. J.; Ralph, F. M.; Minnis, P.; Prather, K. A.

    2015-06-01

    Aerosols that serve as cloud condensation nuclei (CCN) and ice nuclei (IN) have the potential to profoundly influence precipitation processes. Furthermore, changes in orographic precipitation have broad implications for reservoir storage and flood risks. As part of the CalWater field campaign (2009-2011), the variability and associated impacts of different aerosol sources on precipitation were investigated in the California Sierra Nevada using an aerosol time-of-flight mass spectrometer for precipitation chemistry, S-band profiling radar for precipitation classification, remote sensing measurements of cloud properties, and surface meteorological measurements. The composition of insoluble residues in precipitation samples collected at a surface site contained mostly local biomass burning and long-range-transported dust and biological particles (2009), local sources of biomass burning and pollution (2010), and long-range transport (2011). Although differences in the sources of insoluble residues were observed from year to year, the most consistent source of dust and biological residues were associated with storms consisting of deep convective cloud systems with significant quantities of precipitation initiated in the ice phase. Further, biological residues were dominant (up to 40%) during storms with relatively warm cloud temperatures (up to -15 °C), supporting the important role bioparticles can play as ice nucleating particles. On the other hand, lower percentages of residues from local biomass burning and pollution were observed over the three winter seasons (on average 31 and 9%, respectively). When precipitation quantities were relatively low, these insoluble residues most likely served as CCN, forming smaller more numerous cloud droplets at the base of shallow cloud systems, and resulting in less efficient riming processes. Ultimately, the goal is to use such observations to improve the mechanistic linkages between aerosol sources and precipitation processes

  8. Aerosol impacts in the Met Office global NWP model

    NASA Astrophysics Data System (ADS)

    Mulcahy, Jane P.; Brooks, Malcolm E.; Milton, Sean F.

    2010-05-01

    An accurate representation of the direct and indirect effect of aerosols is of growing concern for global numerical weather prediction (NWP). Increased scattering and absorption of incoming shortwave (SW) and outgoing longwave radiation (OLR) fields due to the presence of aerosol layers in the atmosphere modifies the atmospheric heating profile and can affect large-scale circulation patterns. The current representation of aerosols in the global NWP configuration of the Met Office Unified ModelTM (MetUM) is based on a simple aerosol climatology (Cusack et al., 1998). Profiles of water soluble dust, soot, oceanic and stratospheric sulphate aerosols are described separately for land and ocean surfaces and are distributed over the boundary layer, free troposphere and stratosphere (sulphates only). While this improved the reflected SW radiative bias at the top-of-atmosphere (TOA), there is evidence that the climatology is too absorbing leading to a temperature bias in the lower troposphere of approximately 0.5 K/day. Furthermore, the omission of the scattering and absorption properties of mineral dust and biomass burning aerosol particles in particular, is believed to be the principal cause of significant model biases (in the region of 50-56 W m-2) in both the model OLR at the TOA (Haywood et al., 2005) and the surface SW radiation fields (Milton et al., 2008). One of the objectives of the Global Aerosols (G-AER) component of the MACC (Monitoring Atmospheric Composition and Climate) project is to evaluate the impact of an improved aerosol representation on the performance of global NWP models. In a stepwise approach of increasing the aerosol complexity in the MetUM, the Cusack climatology is being replaced by the CLASSIC (Coupled Large-scale Aerosol Simulator for Studies in Climate) aerosol scheme, developed for the HadGEM (Hadley Centre Global Environmental Model) climate model. CLASSIC includes representations of external mixtures of sulphate, black carbon, organic

  9. Distributions of Beryllium 7 and Lead 210, and Soluble Aerosol-Associated Ionic Species Over the Western Pacific: PEM West B

    NASA Technical Reports Server (NTRS)

    Didd, J. E.; Talbot, R. W.; Lefer, B. L.; Scheuer, E.; Gregory, G. L.; Browell, E. V.; Sandholm, S. T.; Singh, H. B.

    1997-01-01

    Aerosol sampling for the determination of the concentrations of soluble ionic species and the natural radionuclides Be-7 and Pb-210 was conducted from the NASA DC-8 over the western Pacific as part of GTE/PEM-West B during February - March 1994. Concentrations of most soluble ionic species in the free troposphere were higher in samples collected on flights originating from Hong Kong and Japan than those collected further east over the open ocean. In both regions the measured concentrations were higher than those found during PEM-West A (fall 1991). Activities of Pb-210 tracer of air masses influenced by sources on the Asian continent, showed the same patterns. These data indicate the effect of stronger continental outflow from Asia over the western Pacific during the spring compared to fall season. For readily scavenged aerosol-associated species and soluble acidic gases the strongest indications of Asian outflow were restricted to altitudes below 6 km. The distribution of the continental tracer Pb-210 was also compared to those of a large number of gas phase species measured on the DC-8. Relatively strong correlations were found with O3 and peroxyacetylnitrate (PAN), but only during the flights over the remote Pacific. During PEM-West A, similar correlations were seen, but they were stronger near Asia. We believe that these correlations are a signature of continental air that has been processed by deep wet convection over land before being advected over the ocean. One flight over the Sea of Japan provided the opportunity to sample upper troposphere/lower stratosphere air in and around a tropopause fold. Concentrations of Be-7 reached 7 pCi/cu m STP, and peak O3, mixing ratios of 480 ppb were encountered at 10.7 km. The Be-7 data are used to estimate the fraction of stratospheric air mixed down into the troposphere by circulation in the fold.

  10. Distributions of Beryllium 7 and Lead 210, and Soluble Aerosol-Associated Ionic Species Over the Western Pacific: PEM West B, February - March 1994

    NASA Technical Reports Server (NTRS)

    Dibb, J. E.; Talbot, R. W.; Lefer, B. L.; Scheuer, E.; Gregory, G. L.; Browell, E. V.; Bradshaw, J. D.; Sandholm, S. T.; Singh, H. B.

    1997-01-01

    Aerosol sampling for the determination of the concentrations of soluble ionic species and the natural radionuclides Be-7 and Pb-210 was conducted from the NASA DC-8 over the western Pacific as part of GTE/PEM-West B during February - March 1994. Concentrations of most soluble ionic species in the free troposphere were higher in samples collected on flights originating from Hong Kong and Japan than those collected further east over the open ocean. In both regions the measured concentrations were higher than those found during PEM-West A (fall 1991). Activities of Pb-210, a tracer of air masses influenced by sources on the Asian continent, showed the same patterns. These data indicate the effect of stronger continental outflow from Asia over the western Pacific during the spring compared to fall season. For readily scavenged aerosol-associated species and soluble acidic gases the strongest indications of Asian outflow were restricted to altitudes below 6 km. The distribution of the continental tracer Pb-210 was also compared to those of a large number of gas phase species measured on the DC-8. Relatively strong correlations were found with O3, and peroxyacetylnitrate (PAN), but only during the flights over the remote Pacific. During PEM-West A, similar correlations were seen, but they were stronger near Asia. We believe that correlations are a signature of continental air that has been processed by deep wet convection over land before being advected over the ocean. One flight over the Sea of Japan provided the opportunity to sample upper troposphere/lower stratosphere air in and around a tropopause fold. Concentrations of Be-7 reached 7 pCi/cu m STP, and peak O3, mixing ratios of 480 ppb were encountered at 10.7 km. The Be-7 data are used to estimate the fraction of stratospheric air mixed down into the troposphere by circulation in the fold.

  11. Coupled Aerosol-Chemistry-Climate Twentieth-Century Transient Model Investigation: Trends in Short-Lived Species and Climate Responses

    NASA Technical Reports Server (NTRS)

    Koch, Dorothy; Bauer, Susanne E.; Del Genio, Anthony; Faluvegi, Greg; McConnell, Joseph R.; Menon, Surabi; Miller, Ronald L.; Rind, David; Ruedy, Reto; Schmidt, Gavin A.; Shindell, Drew

    2011-01-01

    The authors simulate transient twentieth-century climate in the Goddard Institute for Space Studies (GISS) GCM, with aerosol and ozone chemistry fully coupled to one another and to climate including a full dynamic ocean. Aerosols include sulfate, black carbon (BC), organic carbon, nitrate, sea salt, and dust. Direct and BC snow-albedo radiative effects are included. Model BC and sulfur trends agree fairly well with records from Greenland and European ice cores and with sulfur deposition in North America; however, the model underestimates the sulfur decline at the end of the century in Greenland. Global BC effects peak early in the century (1940s); afterward the BC effects decrease at high latitudes of the Northern Hemisphere but continue to increase at lower latitudes. The largest increase in aerosol optical depth occurs in the middle of the century (1940s-80s) when sulfate forcing peaks and causes global dimming. After this, aerosols decrease in eastern North America and northern Eurasia leading to regional positive forcing changes and brightening. These surface forcing changes have the correct trend but are too weak. Over the century, the net aerosol direct effect is -0.41 Watts per square meter, the BC-albedo effect is -0.02 Watts per square meter, and the net ozone forcing is +0.24 Watts per square meter. The model polar stratospheric ozone depletion develops, beginning in the 1970s. Concurrently, the sea salt load and negative radiative flux increase over the oceans around Antarctica. Net warming over the century is modeled fairly well; however, the model fails to capture the dynamics of the observedmidcentury cooling followed by the late century warming.Over the century, 20% of Arctic warming and snow ice cover loss is attributed to the BC albedo effect. However, the decrease in this effect at the end of the century contributes to Arctic cooling. To test the climate responses to sulfate and BC pollution, two experiments were branched from 1970 that removed

  12. Quantifying the Aerosol Semi-Direct Effect in the NASA GEOS-5 AGCM

    NASA Technical Reports Server (NTRS)

    Randles, Cynthia A.; Colarco, Peter R.; daSilva, Arlindo

    2011-01-01

    Aerosols such as black carbon, dust, and some organic carbon species both scatter and absorb incoming solar radiation. This direct aerosol radiative forcing (DARF) redistributes solar energy both by cooling the surface and warming the atmosphere. As a result, these aerosols affect atmospheric stability and cloud cover (the semi-direct effect, or SDE). Furthermore, in regions with persistent high loadings of absorbing aerosols (e.g. Asia), regional circulation patterns may be altered, potentially resulting in changes in precipitation patterns. Here we investigate aerosol-climate coupling using the NASA Goddard Earth Observing System model version 5 (GEOS-5) atmospheric general circulation model (AGCM), in which we have implemented an online version of the Goddard Chemistry, Aerosol, Radiation and Transport (GOCART) model. GOCART includes representations of the sources, sinks, and chemical transformation of externally mixed dust, sea salt, sulfate, and carbonaceous aerosols. We examine a series of free-running ensemble climate simulations of the present-day period (2000-2009) forced by observed sea surface temperatures to determine the impact of aerosols on the model climate. The SDE and response of each simulation is determined by differencing with respect to the control simulation (no aerosol forcing). In a free-running model, any estimate of the SDE includes changes in clouds due both to atmospheric heating from aerosols and changes in circulation. To try and quantify the SDE without these circulation changes we then examine the DARF and SDE in GEOS-5 with prescribed meteorological analyses introduced by the MERRA analysis. By doing so, we are able to examine changes in model clouds that occur on shorter scales (six hours). In the GEOS-5 data assimilation system (DAS), the analysis is defined as the best estimate of the atmospheric state at any given time, and it is determined by optimally combining a first-guess short-term GCM forecast with all available

  13. Contribution of water-soluble and insoluble components and their hydrophobic/hydrophilic subfractions to the reactive oxygen species-generating potential of fine ambient aerosols.

    PubMed

    Verma, Vishal; Rico-Martinez, Roberto; Kotra, Neel; King, Laura; Liu, Jiumeng; Snell, Terry W; Weber, Rodney J

    2012-10-16

    Relative contributions of water- and methanol-soluble compounds and their hydrophobic/hydrophilic subfractions to the ROS (reactive oxygen species)-generating potential of ambient fine aerosols (D(p) < 2.5 μm) are assessed. ROS-generating (or oxidative) potential of the particulate matter (PM) was measured by the dithiothreitol (DTT) assay. Particles were collected on quartz filters (N = 8) at an urban site near central Atlanta during January-February 2012 using a PM(2.5) high-volume sampler. Filter punches were extracted separately in both water and methanol. Hydrophobic and hydrophilic fractions were then subsequently segregated via a C-18 solid phase extraction column. The DTT assay response was significantly higher for the methanol extract, and for both extracts a substantial fraction of PM oxidative potential was associated with the hydrophobic compounds as evident from a substantial attenuation in DTT response after passing PM extracts through the C-18 column (64% for water and 83% for methanol extract; both median values). The DTT activities of water and methanol extracts were correlated with the water-soluble (R = 0.86) and water-insoluble organic carbon (R = 0.94) contents of the PM, respectively. Brown carbon (BrC), which predominantly represents the hydrophobic organic fraction (referred to as humic-like substances, HULIS), was also correlated with DTT activity in both the water (R = 0.78) and methanol extracts (R = 0.83). Oxidative potential was not correlated with any metals measured in the extracts. These findings suggest that the hydrophobic components of both water-soluble and insoluble organic aerosols substantially contribute to the oxidative properties of ambient PM. Further investigation of these hydrophobic organic compounds could help identify sources of a significant fraction of ambient aerosol toxicity.

  14. Water-soluble ions species of size-resolved aerosols: Implications for the atmospheric acidity in São Paulo megacity, Brazil

    NASA Astrophysics Data System (ADS)

    Vieira-Filho, Marcelo; Pedrotti, Jairo J.; Fornaro, Adalgiza

    2016-11-01

    Over the last decade, an increase of ammonium salts in atmospheric deposition has been reported worldwide, especially in megacities. The present study aims to give a better comprehension analysis about particulate matter acidity in São Paulo megacity (MASP), Brazil. Size-resolved aerosols were sampled in MASP, during 2012 winter, showing a bimodal mass concentration distribution, with sulfate concentration exceeding 3.40 μg m- 3, which accounted for over 25% of PM0.56 mass. Regarding the relative distribution of ionic species, 90% of NH4+ levels, were restricted to smaller than 1 μm diameter range. The average neutralization index for PM < 1 μm was 0.62, which indicated an ammonia-limiting atmosphere due to partial neutralization of atmospheric acids. Particles of the accumulation mode presented more acid behavior than other aerosol fractions, with pH value as low as 4.15 in PM0.56. The total neutralization index registered the lowest value for PM0.56, but it did not respond promptly to aerosol variations as the E-AIM model predictions. The highest discrepancies between the acidity proxies occurred in the smaller fractions of particulate matter, especially in the after-filter (AF) stage (diameter < 0.020 μm). In addition, AF stage had the highest contribution to PM total mass, about 14% for all the stages analyzed. Such contribution indicates that acidity in ultrafine particles are still mixed for the MASP and need further investigation.

  15. Chemical characterization of biogenic secondary organic aerosol generated from plant emissions under baseline and stressed conditions: inter- and intra-species variability for six coniferous species

    NASA Astrophysics Data System (ADS)

    Faiola, C. L.; Wen, M.; VanReken, T. M.

    2015-04-01

    The largest global source of secondary organic aerosol (SOA) in the atmosphere is derived from the oxidation of biogenic emissions. Plant stressors associated with a changing environment can alter both the quantity and composition of the compounds that are emitted. Alterations to the biogenic volatile organic compound (BVOC) profile could impact the characteristics of the SOA formed from those emissions. This study investigated the impacts of one global change stressor, increased herbivory, on the composition of SOA derived from real plant emissions. Herbivory was simulated via application of methyl jasmonate (MeJA), a proxy compound. Experiments were repeated under pre- and post-treatment conditions for six different coniferous plant types. Volatile organic compounds (VOCs) emitted from the plants were oxidized to form SOA via dark ozone-initiated chemistry. The SOA chemical composition was measured using a Aerodyne high-resolution time-of-flight aerosol mass spectrometer (HR-AMS). The aerosol mass spectra of pre-treatment biogenic SOA from all plant types tended to be similar with correlations usually greater than or equal to 0.90. The presence of a stressor produced characteristic differences in the SOA mass spectra. Specifically, the following m/z were identified as a possible biogenic stress AMS marker with the corresponding HR ion(s) shown in parentheses: m/z 31 (CH3O+), m/z 58 (C2H2O2+, C3H6O+), m/z 29 (C2H5+), m/z 57 (C3H5O+), m/z 59 (C2H3O2+, C3H7O+), m/z 71 (C3H3O2+, C4H7O+), and m/z 83 (C5H7O+). The first aerosol mass spectrum of SOA generated from the oxidation of the plant stress hormone, MeJA, is also presented. Elemental analysis results demonstrated an O : C range of baseline biogenic SOA between 0.3 and 0.47. The O : C of standard MeJA SOA was 0.52. Results presented here could be used to help identify a biogenic plant stress marker in ambient data sets collected in forest environments.

  16. Chemical characterization of biogenic secondary organic aerosol generated from plant emissions under baseline and stressed conditions: inter- and intra-species variability for six coniferous species

    DOE PAGES

    Faiola, C. L.; Wen, M.; VanReken, T. M.

    2015-04-01

    The largest global source of secondary organic aerosol (SOA) in the atmosphere is derived from the oxidation of biogenic emissions. Plant stressors associated with a changing environment can alter both the quantity and composition of the compounds that are emitted. Alterations to the biogenic volatile organic compound (BVOC) profile could impact the characteristics of the SOA formed from those emissions. This study investigated the impacts of one global change stressor, increased herbivory, on the composition of SOA derived from real plant emissions. Herbivory was simulated via application of methyl jasmonate (MeJA), a proxy compound. Experiments were repeated under pre- andmore » post-treatment conditions for six different coniferous plant types. Volatile organic compounds (VOCs) emitted from the plants were oxidized to form SOA via dark ozone-initiated chemistry. The SOA chemical composition was measured using a Aerodyne high-resolution time-of-flight aerosol mass spectrometer (HR-AMS). The aerosol mass spectra of pre-treatment biogenic SOA from all plant types tended to be similar with correlations usually greater than or equal to 0.90. The presence of a stressor produced characteristic differences in the SOA mass spectra. Specifically, the following m/z were identified as a possible biogenic stress AMS marker with the corresponding HR ion(s) shown in parentheses: m/z 31 (CH3O+), m/z 58 (C2H2O2+, C3H6O+), m/z 29 (C2H5+), m/z 57 (C3H5O+), m/z 59 (C2H3O2+, C3H7O+), m/z 71 (C3H3O2+, C4H7O+), and m/z 83 (C5H7O+). The first aerosol mass spectrum of SOA generated from the oxidation of the plant stress hormone, MeJA, is also presented. Elemental analysis results demonstrated an O : C range of baseline biogenic SOA between 0.3 and 0.47. The O : C of standard MeJA SOA was 0.52. Results presented here could be used to help identify a biogenic plant stress marker in ambient data sets collected in forest environments.« less

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

    NASA Astrophysics Data System (ADS)

    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.

  18. Identification of nitrogenous organic species in Titan aerosols analogs: Implication for prebiotic chemistry on Titan and early Earth

    NASA Astrophysics Data System (ADS)

    He, Chao; Smith, Mark A.

    2014-08-01

    Titan has a significant atmosphere composed primarily of nitrogen and methane with a significant organic haze component. Its nitrogen-rich atmosphere, abundant organics, and liquid surface make this moon of interest as a prebiotic laboratory at the planetary scale and one of the best targets for studying prebiotic planetary organic chemistry. In our previous work, we have investigated the chemical composition of Titan aerosol analogs (tholins) and identified a variety of nitrogenous organic molecules. Here we continue our structural investigation and identify four important prebiotic molecules in Titan tholins using NMR, GC-MS and standard sample comparison, including aminoacetonitrile, succinonitrile, acetoguanamine and adenine. On the basis of their structural characteristics, we suggest their formation pathways via simple precursors including methanimine (CH2NH), HCN, NH3, CH3CN and C2H2 in laboratory N2sbnd CH4 plasma or potentially in Titan’s atmosphere. Among these molecules, aminoacetonitrile is a potential precursor of amino acids and peptides, while adenine is a necessary ingredient for DNA and RNA. The identification of these molecules in Titan’s organic aerosol analogs increases our knowledge of Titan’s organic chemistry and its prebiotic implications.

  19. Aerosol-Water Cycle Interaction: A New Challenge in Monsoon Climate Research

    NASA Technical Reports Server (NTRS)

    Lau, William K. M.

    2006-01-01

    Long recognized as a major environmental hazard, aerosol is now known to have strong impacts on both regional and global climate. It has been estimated that aerosol may reduce by up to 10% of the seasonal mean solar radiation reaching the earth surface, producing a global cooling effect that opposes global warming (Climate Change 2001). This means that the potential perils that humans have committed to global warming may be far greater than what we can detect at the present. As a key component of the Earth climate system, the water cycle is profoundly affected by the presence of aerosols in the atmosphere. Through the so-called direct effect , aerosol scatters and/or absorbs solar radiation, thus cooling the earth surface and changing the horizontal and vertical radiational heating contrast in the atmosphere. The heating contrast drives anomalous atmospheric circulation, resulting in changes in convection, clouds, and rainfall. Another way aerosol can affect the water cycle is through the so-called indirect effects, whereby aerosol increases the number of cloud condensation nuclei, prolongs life time of clouds, and inhibits the growth of cloud drops to raindrops. This leads to more clouds, and increased reflection of solar radiation, and further cooling at the earth surface. In monsoon regions, the response of the water cycle to aerosol forcing is especially complex, not only because of presence of diverse mix of aerosol species with vastly different radiative properties, but also because the monsoon is strongly influenced by ocean and land surface processes, land use, land change, as well as regional and global greenhouse warming effects. Thus, sorting out the impacts of aerosol forcing, and interaction with the monsoon water cycle is a very challenging problem. In this talk, I will offer some insights into how aerosols may impact the Asian monsoon based on preliminary results from satellite observations and climate model experiments. Specifically, I will discuss

  20. Aerosol-Water Cycle Interaction: A New Challenge in Monsoon Climate Research

    NASA Technical Reports Server (NTRS)

    Lau, William K. M.

    2006-01-01

    Long recognized as a major environmental hazard, aerosol is now known to have strong impacts on both regional and global climate. It has been estimated that aerosol may reduce by up to 10% of the seasonal mean solar radiation reaching the earth surface, producing a global cooling effect that opposes global warming (Climate Change 2001). This means that the potential perils that humans have committed to global warming may be far greater than what we can detect at the present. As a key component of the Earth climate system, the water cycle is profoundly affected by the presence of aerosols in the atmosphere. Through the so-called "direct effect", aerosol scatters and/or absorbs solar radiation, thus cooling the earth surface and changing the horizontal and vertical radiational heating contrast in the atmosphere. The heating contrast drives anomalous atmospheric circulation, resulting in changes in convection, clouds, and rainfall. Another way aerosol can affect the water cycle is through the so-called "indirect effects", whereby aerosol increases the number of cloud condensation nuclei, prolongs life time of clouds, and inhibits the growth of cloud drops to raindrops. This leads to more clouds, and increased reflection of solar radiation, and further cooling at the earth surface. In monsoon regions, the response of the water cycle to aerosol forcing is especially complex, not only because of presence of diverse mix of aerosol species with vastly different radiative properties, but also because the monsoon is strongly influenced by ocean and land surface processes, land use, land change, as well as regional and global greenhouse warming effects. Thus, sorting out the impacts of aerosol forcing, and interaction with the monsoon water cycle is a very challenging problem. In this talk, I will offer some insights into how aerosols may impact the Asian monsoon based on preliminary results from satellite observations and climate model experiments. Specifically, I will

  1. Organic aerosols and inorganic species from post-harvest agricultural-waste burning emissions over northern India: impact on mass absorption efficiency of elemental carbon.

    PubMed

    Rajput, Prashant; Sarin, M M; Sharma, Deepti; Singh, Darshan

    2014-01-01

    Atmospheric PM2.5 (particulate matter with aerodynamic diameter of ≤ 2.5 μm), collected from a source region [Patiala: 30.2 °N; 76.3 °E; 250 m above mean sea level] of emissions from post-harvest agricultural-waste (paddy-residue) burning in the Indo-Gangetic Plain (IGP), North India, has been studied for its chemical composition and impact on regional atmospheric radiative forcing. On average, organic aerosol mass accounts for 63% of PM2.5, whereas the contribution of elemental carbon (EC) is ∼3.5%. Sulphate, nitrate and ammonium contribute up to ∼85% of the total water-soluble inorganic species (WSIS), which constitutes ∼23% of PM2.5. The potassium-to-organic carbon ratio from paddy-residue burning emissions (KBB(+)/OC: 0.05 ± 0.01) is quite similar to that reported from Amazonian and Savanna forest-fires; whereas non-sea-salt-sulphate-to-OC ratio (nss-SO4(2-)/OC: 0.21) and nss-SO4(2-)/EC ratio of 2.6 are significantly higher (by factor of 5 to 8). The mass absorption efficiency of EC (3.8 ± 1.3 m(2) g(-1)) shows significant decrease with a parallel increase in the concentrations of organic aerosols and scattering species (sulphate and nitrate). A cross plot of OC/EC and nss-SO4(2-)/EC ratios show distinct differences for post-harvest burning emissions from paddy-residue as compared to those from fossil-fuel combustion sources in south-east Asia.

  2. Laboratory Experiments and Instrument Intercomparison Studies of Carbonaceous Aerosol Particles

    SciTech Connect

    Davidovits, Paul

    2015-10-20

    Aerosols containing black carbon (and some specific types of organic particulate matter) directly absorb incoming light, heating the atmosphere. In addition, all aerosol particles backscatter solar light, leading to a net-cooling effect. Indirect effects involve hydrophilic aerosols, which serve as cloud condensation nuclei (CCN) that affect cloud cover and cloud stability, impacting both atmospheric radiation balance and precipitation patterns. At night, all clouds produce local warming, but overall clouds exert a net-cooling effect on the Earth. The effect of aerosol radiative forcing on climate may be as large as that of the greenhouse gases, but predominantly opposite in sign and much more uncertain. The uncertainties in the representation of aerosol interactions in climate models makes it problematic to use model projections to guide energy policy. The objective of our program is to reduce the uncertainties in the aerosol radiative forcing in the two areas highlighted in the ASR Science and Program Plan. That is, (1) addressing the direct effect by correlating particle chemistry and morphology with particle optical properties (i.e. absorption, scattering, extinction), and (2) addressing the indirect effect by correlating particle hygroscopicity and CCN activity with particle size, chemistry, and morphology. In this connection we are systematically studying particle formation, oxidation, and the effects of particle coating. The work is specifically focused on carbonaceous particles where the uncertainties in the climate relevant properties are the highest. The ongoing work consists of laboratory experiments and related instrument inter-comparison studies both coordinated with field and modeling studies, with the aim of providing reliable data to represent aerosol processes in climate models. The work is performed in the aerosol laboratory at Boston College. At the center of our laboratory setup are two main sources for the production of aerosol particles: (a

  3. Unified Aerosol Microphysics for NWP

    DTIC Science & Technology

    2011-09-30

    Specifically, the goal is to develop a COAMPS that is capable of simulating the full range of interactions between aerosol particles, clouds , and radiative...aerosol species that are responsible for degradation of Electro- Optical (EO) propagation or that modify cloud behavior and lifetime. Report...enabling new development of more complex cloud -aerosol interactions. The work on this project has been divided into two phases, an investigation phase

  4. Size-resolved airborne particulate oxalic and related secondary organic aerosol species in the urban atmosphere of Chengdu, China

    NASA Astrophysics Data System (ADS)

    Cheng, Chunlei; Wang, Gehui; Meng, Jingjing; Wang, Qiyuan; Cao, Junji; Li, Jianjun; Wang, Jiayuan

    2015-07-01

    Size-segregated (9-stages) airborne particles during winter in Chengdu city of China were collected on a day/night basis and determined for dicarboxylic acids (diacids), ketocarboxylic acids (ketoacids), α-dicarbonyls, inorganic ions, and water-soluble organic carbon and nitrogen (WSOC and WSON). Diacid concentration was higher in nighttime (1831 ± 607 ng m- 3) than in daytime (1532 ± 196 ng m- 3), whereas ketoacids and dicarbonyls showed little diurnal difference. Most of the organic compounds were enriched in the fine mode (< 2.1 μm) with a peak at the size range of 0.7-2.1 μm. In contrast, phthalic acid (Ph) and glyoxal (Gly) presented two equivalent peaks in the fine and coarse modes, which is at least in part due to the gas-phase oxidation of precursors and a subsequent partitioning into pre-existing particles. Liquid water content (LWC) of the fine mode particles was three times higher in nighttime than in daytime. The calculated in-situ pH (pHis) indicated that all the fine mode aerosols were acidic during the sampling period and more acidic in daytime than in nighttime. Robust correlations of the ratios of glyoxal/oxalic acid (Gly/C2) and glyoxylic acid/oxalic acid (ωC2/C2) with LWC in the samples suggest that the enhancement of LWC is favorable for oxidation of Gly and ωC2 to produce C2. Abundant K+ and Cl- in the fine mode particles and the strong correlations of K+ with WSOC, WSON and C2 indicate that secondary organic aerosols in the city are significantly affected by biomass burning emission.

  5. Organic aerosols

    SciTech Connect

    Penner, J.E.

    1994-01-01

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

  6. Global Aerosol Optical Models and Lookup Tables for the New MODIS Aerosol Retrieval over Land

    NASA Technical Reports Server (NTRS)

    Levy, Robert C.; Remer, Loraine A.; Dubovik, Oleg

    2007-01-01

    Since 2000, MODIS has been deriving aerosol properties over land from MODIS observed spectral reflectance, by matching the observed reflectance with that simulated for selected aerosol optical models, aerosol loadings, wavelengths and geometrical conditions (that are contained in a lookup table or 'LUT'). Validation exercises have showed that MODIS tends to under-predict aerosol optical depth (tau) in cases of large tau (tau greater than 1.0), signaling errors in the assumed aerosol optical properties. Using the climatology of almucantur retrievals from the hundreds of global AERONET sunphotometer sites, we found that three spherical-derived models (describing fine-sized dominated aerosol), and one spheroid-derived model (describing coarse-sized dominated aerosol, presumably dust) generally described the range of observed global aerosol properties. The fine dominated models were separated mainly by their single scattering albedo (omega(sub 0)), ranging from non-absorbing aerosol (omega(sub 0) approx. 0.95) in developed urban/industrial regions, to neutrally absorbing aerosol (omega(sub 0) approx.90) in forest fire burning and developing industrial regions, to absorbing aerosol (omega(sub 0) approx. 0.85) in regions of savanna/grassland burning. We determined the dominant model type in each region and season, to create a 1 deg. x 1 deg. grid of assumed aerosol type. We used vector radiative transfer code to create a new LUT, simulating the four aerosol models, in four MODIS channels. Independent AERONET observations of spectral tau agree with the new models, indicating that the new models are suitable for use by the MODIS aerosol retrieval.

  7. Global aerosol optical properties and application to Moderate Resolution Imaging Spectroradiometer aerosol retrieval over land

    NASA Astrophysics Data System (ADS)

    Levy, Robert C.; Remer, Lorraine A.; Dubovik, Oleg

    2007-07-01

    As more information about global aerosol properties has become available from remotely sensed retrievals and in situ measurements, it is prudent to evaluate this new information, both on its own and in the context of satellite retrieval algorithms. Using the climatology of almucantur retrievals from global Aerosol Robotic Network (AERONET) Sun photometer sites, we perform cluster analysis to determine aerosol type as a function of location and season. We find that three spherical-derived types (describing fine-sized dominated aerosol) and one spheroid-derived types (describing coarse-sized dominated aerosol, presumably dust) generally describe the range of AERONET observed global aerosol properties. The fine-dominated types are separated mainly by their single scattering albedo (ω0), ranging from nonabsorbing aerosol (ω0 ˜ 0.95) in developed urban/industrial regions, to moderately absorbing aerosol (ω0 ˜ 0.90) in forest fire burning and developing industrial regions, to absorbing aerosol (ω0 ˜ 0.85) in regions of savanna/grassland burning. We identify the dominant aerosol type at each site, and extrapolate to create seasonal 1° × 1° maps of expected aerosol types. Each aerosol type is bilognormal, with dynamic (function of optical depth) size parameters (radius, standard deviation, volume distribution) and complex refractive index. Not only are these parameters interesting in their own right, they can also be applied to aerosol retrieval algorithms, such as to aerosol retrieval over land from Moderate Resolution Imaging Spectroradiometer. Independent direct-Sun AERONET observations of spectral aerosol optical depth (τ) are consistent the spectral dependence of the models, indicating that our derived aerosol models are relevant.

  8. Infrared spectroscopy of aerosols

    NASA Astrophysics Data System (ADS)

    Mentel, Th.; Sebald, H.

    2003-04-01

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

  9. Determination of aerosol ammonium using an aerodyne aerosol mass spectrometer

    NASA Astrophysics Data System (ADS)

    Delia, A. E.; Toohey, D. W.; Worsnop, D. R.

    2003-04-01

    The chemical composition of fine aerosols is a significant issue both because it influences the chemical and radiative properties of the aerosols, which in turn impact the regional and global climate and human health, and because it is difficult to measure accurately. The Aerosol Mass Spectrometer (AMS) developed by Aerodyne Research measures both chemical composition and aerodynamic size of submicron aerosols quantitatively. However, the measurement of aerosol ammonium is more difficult than that of the other major inorganic species, nitrate and sulfate, because of interferences in the mass spectrum from air and water. This presentation will describe the successful procedure developed for dealing with these interferences and accurately determining the ammonium mass. In addition, the application of this procedure to aerosols from a range of ambient conditions will be demonstrated using data from several field studies.

  10. Spectral Absorption of Solar Radiation by Aerosols during ACE-Asia

    NASA Technical Reports Server (NTRS)

    Bergstrom, R. W.; Pilewskie, P.; Pommier, J.; Rabbette, M.; Russell, P. B.; Schmid, B.; Redermann, J.; Higurashi, A.; Nakajima, T.; Quinn, P. K.

    2004-01-01

    As part of the Asian Pacific Regional Aerosol Characterization Experiment (ACE-Asia), the upward and downward spectral solar radiant fluxes were measured with the Spectral Solar Flux Radiometer (SSFR), and the aerosol optical depth was measured with the Ames Airborne Tracking Sunphotometer (AATS-14) aboard the Center for INterdisciplinary Remotely-Piloted Aircraft Studies (CIRPAS) Twin Otter aircraft. IN this paper, we examine the data obtained for two cases: a moderately thick aerosol layer, 12 April, and a relatively thin aerosol case, 16 April 2001. ON both days, the Twin Otter flew vertical profiles in the Korean Strait southeast of Gosan Island. For both days we determine the aerosol spectral absorption of the layer and estimate the spectral aerosol absorption optical depth and single-scattering albedo. The results for 12 April show that the single-scattering albedo increases with wavelength from 0.8 at 400 nm to 0.95 at 900 nm and remains essentially constant from 950 to 1700 nm. On 16 April the amount of aerosol absorption was very low; however, the aerosol single-scattering albedo appears to decrease slightly with wavelength in the visible region. We interpret these results in light of the two absorbing aerosol species observed during the ACE-asia study: mineral dust and black carbon. The results for 12 April are indicative of a mineral dust-black carbon mixture. The 16 April results are possibly caused by black carbon mixed with nonabsorbing pollution aerosols. For the 12 April case we attempt to estimate the relative contributions of the black carbon particles and the mineral dust particles. We compare our results with other estimates of the aerosol properties from a Sea-Viewing Wide Field-of-View Sensor (SeaWiFS) satellite analysis and aerosol measurements made aboard the Twin Otter, aboard the National Oceanic and Atmospheric Administration Ronald H Brown ship, and at ground sites in Gosan and Japan. The results indicate a relatively complicated aerosol

  11. A satellite view of aerosols in the climate system

    NASA Technical Reports Server (NTRS)

    Kaufman, Yoram J.; Tanre, Didier; Boucher, Olivier

    2002-01-01

    Anthropogenic aerosols are intricately linked to the climate system and to the hydrologic cycle. The net effect of aerosols is to cool the climate system by reflecting sunlight. Depending on their composition, aerosols can also absorb sunlight in the atmosphere, further cooling the surface but warming the atmosphere in the process. These effects of aerosols on the temperature profile, along with the role of aerosols as cloud condensation nuclei, impact the hydrologic cycle, through changes in cloud cover, cloud properties and precipitation. Unravelling these feedbacks is particularly difficult because aerosols take a multitude of shapes and forms, ranging from desert dust to urban pollution, and because aerosol concentrations vary strongly over time and space. To accurately study aerosol distribution and composition therefore requires continuous observations from satellites, networks of ground-based instruments and dedicated field experiments. Increases in aerosol concentration and changes in their composition, driven by industrialization and an expanding population, may adversely affect the Earth's climate and water supply.

  12. A satellite view of aerosols in the climate system.

    PubMed

    Kaufman, Yoram J; Tanré, Didier; Boucher, Olivier

    2002-09-12

    Anthropogenic aerosols are intricately linked to the climate system and to the hydrologic cycle. The net effect of aerosols is to cool the climate system by reflecting sunlight. Depending on their composition, aerosols can also absorb sunlight in the atmosphere, further cooling the surface but warming the atmosphere in the process. These effects of aerosols on the temperature profile, along with the role of aerosols as cloud condensation nuclei, impact the hydrologic cycle, through changes in cloud cover, cloud properties and precipitation. Unravelling these feedbacks is particularly difficult because aerosols take a multitude of shapes and forms, ranging from desert dust to urban pollution, and because aerosol concentrations vary strongly over time and space. To accurately study aerosol distribution and composition therefore requires continuous observations from satellites, networks of ground-based instruments and dedicated field experiments. Increases in aerosol concentration and changes in their composition, driven by industrialization and an expanding population, may adversely affect the Earth's climate and water supply.

  13. A Global Data Assimilation System for Atmospheric Aerosol

    NASA Technical Reports Server (NTRS)

    daSilva, Arlindo

    1999-01-01

    We will give an overview of an aerosol data assimilation system which combines advances in remote sensing of atmospheric aerosols, aerosol modeling and data assimilation methodology to produce high spatial and temporal resolution 3D aerosol fields. Initially, the Goddard Aerosol Assimilation System (GAAS) will assimilate TOMS, AVHRR and AERONET observations; later we will include MODIS and MISR. This data assimilation capability will allows us to integrate complementing aerosol observations from these platforms, enabling the development of an assimilated aerosol climatology as well as a global aerosol forecasting system in support of field campaigns. Furthermore, this system provides an interactive retrieval framework for each aerosol observing satellites, in particular TOMS and AVHRR. The Goddard Aerosol Assimilation System (GAAS) takes advantage of recent advances in constituent data assimilation at DAO, including flow dependent parameterizations of error covariances and the proper consideration of model bias. For its prognostic transport model, GAAS will utilize the Goddard Ozone, Chemistry, Aerosol, Radiation and Transport (GOCART) model developed at NASA/GSFC Codes 916 and 910.3. GOCART includes the Lin-Rood flux-form, semi-Langrangian transport model with parameterized aerosol chemistry and physical processes for absorbing (dust and black carbon) and non-absorbing aerosols (sulfate and organic carbon). Observations and model fields are combined using a constituent version of DAO's Physical-space Statistical Analysis System (PSAS), including its adaptive quality control system. In this talk we describe the main components of this assimilation system and present preliminary results obtained by assimilating TOMS data.

  14. Remote Sensing of Aerosol and Aerosol Radiative Forcing of Climate from EOS Terra MODIS Instrument

    NASA Technical Reports Server (NTRS)

    Kaufman, Yoram; Tanre, Didier; Remer, Lorraine; Einaudi, Franco (Technical Monitor)

    2000-01-01

    The recent launch of EOS-Terra into polar orbit has begun to revolutionize remote sensing of aerosol and their effect on climate. Terra has five instruments, two of them,Moderate Resolution Imaging Spectroradiometer (MODIS) and Multiangle Imaging Spectro-Radiometer (MISR) are designed to monitor global aerosol in two different complementary ways. Here we shall discuss the use of the multispectral measurements of MODIS to derive: (1) the global distribution of aerosol load (and optical thickness) over ocean and land; (2) to measure the impact of aerosol on reflection of sunlight to space; and (3) to measure the ability of aerosol to absorb solar radiation. These measurements have direct applications on the understanding of the effect of aerosol on climate, the ability to predict climate change, and on the monitoring of dust episodes and man-made pollution. Principles of remote sensing of aerosol from MODIS will be discussed and first examples of measurements from MODIS will be provided.

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

    SciTech Connect

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

    2012-11-21

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

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

    NASA Astrophysics Data System (ADS)

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

    2012-11-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2012-07-01

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

  18. Effect of aerosol subgrid variability on aerosol optical depth and cloud condensation nuclei: implications for global aerosol modelling

    NASA Astrophysics Data System (ADS)

    Weigum, Natalie; Schutgens, Nick; Stier, Philip

    2016-11-01

    A fundamental limitation of grid-based models is their inability to resolve variability on scales smaller than a grid box. Past research has shown that significant aerosol variability exists on scales smaller than these grid boxes, which can lead to discrepancies in simulated aerosol climate effects between high- and low-resolution models. This study investigates the impact of neglecting subgrid variability in present-day global microphysical aerosol models on aerosol optical depth (AOD) and cloud condensation nuclei (CCN). We introduce a novel technique to isolate the effect of aerosol variability from other sources of model variability by varying the resolution of aerosol and trace gas fields while maintaining a constant resolution in the rest of the model. We compare WRF-Chem (Weather and Research Forecast model) runs in which aerosol and gases are simulated at 80 km and again at 10 km resolutions; in both simulations the other model components, such as meteorology and dynamics, are kept at the 10 km baseline resolution. We find that AOD is underestimated by 13 % and CCN is overestimated by 27 % when aerosol and gases are simulated at 80 km resolution compared to 10 km. The processes most affected by neglecting aerosol subgrid variability are gas-phase chemistry and aerosol uptake of water through aerosol-gas equilibrium reactions. The inherent non-linearities in these processes result in large changes in aerosol properties when aerosol and gaseous species are artificially mixed over large spatial scales. These changes in aerosol and gas concentrations are exaggerated by convective transport, which transports these altered concentrations to altitudes where their effect is more pronounced. These results demonstrate that aerosol variability can have a large impact on simulating aerosol climate effects, even when meteorology and dynamics are held constant. Future aerosol model development should focus on accounting for the effect of subgrid variability on these

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

    NASA Astrophysics Data System (ADS)

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

    2015-12-01

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

  20. Stratospheric Aerosol Measurements

    NASA Technical Reports Server (NTRS)

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

    1998-01-01

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

  1. Using the OMI Aerosol Index and Absorption Aerosol Optical Depth to Evaluate the NASA MERRA Aerosol Reanalysis.

    NASA Astrophysics Data System (ADS)

    Buchard, V.; da Silva, A. M., Jr.; Colarco, P. R.; Darmenov, A.; Govindaraju, R.

    2014-12-01

    A radiative transfer interface has been developed to simulate the UV Aerosol Index (AI) from the NASA Goddard Earth Observing System version 5 (GEOS-5) aerosol assimilated fields. The purpose of this work is to use the AI derived from the Ozone Monitoring Instrument (OMI) measurements as independent validation for the Modern Era Retrospective analysis for Research and Applications Aerosol Reanalysis (MERRAero). In this presentation we show comparisons of model produced AI with the corresponding OMI measurements during several months of 2007 characterized by a good sampling of dust and biomass burning events. In parallel, model produced Absorption Aerosol Optical Depth (AAOD) were compared to OMI AAOD for the same period, identifying regions where the model representation of absorbing aerosols were deficient. Since AI is dependent on aerosol concentration, optical properties and altitude of the aerosol layer, we make use of complementary observations to fully diagnose the model, including AOD from the Multi-angle Imaging SpectroRadiometer (MISR) and the Moderate Resolution Imaging Spectroradiometer (MODIS) sensors, aerosol retrievals from the Aerosol Robotic Network (AERONET) and attenuated backscatter coefficients from the Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observation (CALIPSO) mission to ascertain misplacement of plume height by the model.

  2. Identifying Aerosol Type/Mixture from Aerosol Absorption Properties Using AERONET

    NASA Technical Reports Server (NTRS)

    Giles, D. M.; Holben, B. N.; Eck, T. F.; Sinyuk, A.; Dickerson, R. R.; Thompson, A. M.; Slutsker, I.; Li, Z.; Tripathi, S. N.; Singh, R. P.; Zibordi, G.

    2010-01-01

    Aerosols are generated in the atmosphere through anthropogenic and natural mechanisms. These sources have signatures in the aerosol optical and microphysical properties that can be used to identify the aerosol type/mixture. Spectral aerosol absorption information (absorption Angstrom exponent; AAE) used in conjunction with the particle size parameterization (extinction Angstrom exponent; EAE) can only identify the dominant absorbing aerosol type in the sample volume (e.g., black carbon vs. iron oxides in dust). This AAE/EAE relationship can be expanded to also identify non-absorbing aerosol types/mixtures by applying an absorption weighting. This new relationship provides improved aerosol type distinction when the magnitude of absorption is not equal (e.g, black carbon vs. sulfates). The Aerosol Robotic Network (AERONET) data provide spectral aerosol optical depth and single scattering albedo - key parameters used to determine EAE and AAE. The proposed aerosol type/mixture relationship is demonstrated using the long-term data archive acquired at AERONET sites within various source regions. The preliminary analysis has found that dust, sulfate, organic carbon, and black carbon aerosol types/mixtures can be determined from this AAE/EAE relationship when applying the absorption weighting for each available wavelength (Le., 440, 675, 870nm). Large, non-spherical dust particles absorb in the shorter wavelengths and the application of 440nm wavelength absorption weighting produced the best particle type definition. Sulfate particles scatter light efficiently and organic carbon particles are small near the source and aggregate over time to form larger less absorbing particles. Both sulfates and organic carbon showed generally better definition using the 870nm wavelength absorption weighting. Black carbon generation results from varying combustion rates from a number of sources including industrial processes and biomass burning. Cases with primarily black carbon showed

  3. Composition for absorbing hydrogen

    DOEpatents

    Heung, Leung K.; Wicks, George G.; Enz, Glenn L.

    1995-01-01

    A hydrogen absorbing composition. The composition comprises a porous glass matrix, made by a sol-gel process, having a hydrogen-absorbing material dispersed throughout the matrix. A sol, made from tetraethyl orthosilicate, is mixed with a hydrogen-absorbing material and solidified to form a porous glass matrix with the hydrogen-absorbing material dispersed uniformly throughout the matrix. The glass matrix has pores large enough to allow gases having hydrogen to pass through the matrix, yet small enough to hold the particles dispersed within the matrix so that the hydrogen-absorbing particles are not released during repeated hydrogen absorption/desorption cycles.

  4. Composition for absorbing hydrogen

    DOEpatents

    Heung, L.K.; Wicks, G.G.; Enz, G.L.

    1995-05-02

    A hydrogen absorbing composition is described. The composition comprises a porous glass matrix, made by a sol-gel process, having a hydrogen-absorbing material dispersed throughout the matrix. A sol, made from tetraethyl orthosilicate, is mixed with a hydrogen-absorbing material and solidified to form a porous glass matrix with the hydrogen-absorbing material dispersed uniformly throughout the matrix. The glass matrix has pores large enough to allow gases having hydrogen to pass through the matrix, yet small enough to hold the particles dispersed within the matrix so that the hydrogen-absorbing particles are not released during repeated hydrogen absorption/desorption cycles.

  5. Sources of chemical species in rainwater during monsoon and non-monsoonal periods over two mega cities in India and dominant source region of secondary aerosols

    NASA Astrophysics Data System (ADS)

    Rao, P. S. P.; Tiwari, S.; Matwale, J. L.; Pervez, S.; Tunved, P.; Safai, P. D.; Srivastava, A. K.; Bisht, D. S.; Singh, S.; Hopke, P. K.

    2016-12-01

    Samples of rainwater (RW) were collected to characterize the chemistry and sources in two representative megacities at Pune (Southwest) and Delhi (Northern) India from 2011 to 2014 across two seasons: monsoon (MN) and non-monsoon (NMN). Collected RW samples were analyzed for major chemical constituents (F-, Cl-, SO42-, NO3-, NH4+, Na+, K+, Ca2+, and Mg2+), pH and conductivity. In addition, bicarbonate (HCO3-) was also estimated. The mean pH values of the RW were >6 at Pune and <6 at Delhi and 4% and 26% were acidic, respectively. The mean sum of all measured ionic species in Pune and Delhi was 304.7 and 536.4 μeq/l, respectively, indicating that significant atmospheric pollution effects in these Indian mega cities. Both the Ca2+ and SO42- were the dominant ions, accounting for 43% (Pune) and 54% (Delhi) of the total ions. The sum of measured ions during the NMN period was greater than the NM period by a factor of 1.5 for Pune (278.4: NM and 412.1: NMN μeq/l) and a factor of about 2.5 for Delhi (406 and 1037.7 μeq/l). The contributions of SO42- and NO3- to the RW acidity were ∼40% and 60%, respectively, at Pune and correspondingly, 36% and 64% at Delhi. The concentrations of secondary aerosols (SO42-and NO3-) were higher by a factor of two and three when the air masses were transported to Pune from the continental side. At Delhi, the concentrations of SO42-, NO3-, Ca2+, and Mg2+ were significantly higher when the air masses arrive from Punjab, Haryana, and Pakistan indicating the greater atmospheric pollution over the Indo-Gangetic Plain. Positive matrix factorization was applied to the source apportionment of the deposition fluxes of these ions. Three factors were obtained for Pune and four for Delhi. The sources at Pune were secondary aerosols from fossil fuel combustion, soil dust, and marine, whereas, at Delhi, the sources were soil, fossil fuel combustion, biomass burning, and industrial chlorine.

  6. Formation of a K-In-Se Surface Species by NaF/KF Postdeposition Treatment of Cu(In,Ga)Se2 Thin-Film Solar Cell Absorbers.

    PubMed

    Handick, Evelyn; Reinhard, Patrick; Wilks, Regan G; Pianezzi, Fabian; Kunze, Thomas; Kreikemeyer-Lorenzo, Dagmar; Weinhardt, Lothar; Blum, Monika; Yang, Wanli; Gorgoi, Mihaela; Ikenaga, Eiji; Gerlach, Dominic; Ueda, Shigenori; Yamashita, Yoshiyuki; Chikyow, Toyohiro; Heske, Clemens; Buecheler, Stephan; Tiwari, Ayodhya N; Bär, Marcus

    2017-02-01

    A NaF/KF postdeposition treatment (PDT) has recently been employed to achieve new record efficiencies of Cu(In,Ga)Se2 (CIGSe) thin film solar cells. We have used a combination of depth-dependent soft and hard X-ray photoelectron spectroscopy as well as soft X-ray absorption and emission spectroscopy to gain detailed insight into the chemical structure of the CIGSe surface and how it is changed by different PDTs. Alkali-free CIGSe, NaF-PDT CIGSe, and NaF/KF-PDT CIGSe absorbers grown by low-temperature coevaporation have been interrogated. We find that the alkali-free and NaF-PDT CIGSe surfaces both display the well-known Cu-poor CIGSe chemical surface structure. The NaF/KF-PDT, however, leads to the formation of bilayer structure in which a K-In-Se species covers the CIGSe compound that in composition is identical to the chalcopyrite structure of the alkali-free and NaF-PDT absorber.

  7. Secondary brown carbon - Formation of light-absorbing compounds in atmospheric particulates from selected dicarbonyls and amines

    NASA Astrophysics Data System (ADS)

    Kampf, Christopher; Filippi, Alexander; Hoffmann, Thorsten

    2015-04-01

    One of the main open questions regarding organic compounds in atmospheric chemistry today is related to the formation of optically-active compounds and the occurrence of so called brown carbon (Andreae and Gelencsér, 2006). While organic compounds in ambient fine particles for decades have been assumed to not absorb solar radiation, thus resulting in a net cooling effect on climate (IPCC, 2007), it is now generally accepted that a continuum of light-absorbing carbonaceous species is present in fine aerosols (Pöschl, 2003). In this study, light-absorbing compounds from reactions between dicarbonyl compounds, i.e., glyoxal, methylglyoxal, acetylacetone, 2,3-butanedione, 2,5-hexanedione, and glutaraldehyde, and amine species, i.e., ammonia and glycine, were investigated at atmospherically relevant concentrations in bulk solution experiments mimicking atmospheric particulates. Product analyses were performed using UV/Vis spectrophotometry and (ultra) high performance liquid chromatography coupled to diode array detection and ion trap mass spectrometry (HPLC-DAD-ESI-MS/MS), as well as ultra-high resolution (Orbitrap) mass spectrometry (UHPLC-ESI-HRMS/MS). We demonstrate that light-absorbing compounds are formed from a variety of atmospherically relevant dicarbonyls via particle phase reactions with amine nucleophiles. Single dicarbonyl and mixed dicarbonyl experiments were performed and products were analyzed. The reaction products are suggested to be cyclic nitrogen containing compounds such as imidazoles or dihydropyridines as well as open chain compounds resulting from aldol condensation reactions. Further, the reactive turnover was found to be higher at increasing pH values. The aforementioned processes may be of higher relevance in regions with high aerosol pH, e.g., resulting from high ammonia emissions as for example in northern India (Clarisse et al., 2009). References Andreae, M.O., and Gelencsér, A. (2006): Black carbon or brown carbon? The nature of light-absorbing

  8. SEAC4RS Aerosol Radiative Effects and Heating Rates

    NASA Astrophysics Data System (ADS)

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

    2015-12-01

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

  9. Effect of Increasing Temperature on Carbonaceous Aerosol Direct Radiative Effect over Southeastern US

    NASA Astrophysics Data System (ADS)

    Mielonen, Tero; Kokkola, Harri; Hienola, Anca; Kühn, Thomas; Merikanto, Joonas; Korhonen, Hannele; Arola, Antti; Kolmonen, Pekka; Sogacheva, Larisa; de Leeuw, Gerrit

    2016-04-01

    Aerosols are an important regulator of the Earth's climate. They scatter and absorb incoming solar radiation and thus cool the climate by reducing the amount of energy reaching the atmospheric layers and the surface below (direct effect). A certain subset of the particles can also act as initial formation sites for cloud droplets and thereby modify the microphysics, dynamics, radiative properties and lifetime of clouds (indirect effects). The magnitude of aerosol radiative effects remains the single largest uncertainty in current estimates of anthropogenic radiative forcing. One of the key quantities needed for accurate estimates of anthropogenic radiative forcing is an accurate estimate of the radiative effects from natural unperturbed aerosol. The dominant source of natural aerosols over Earth's vast forested regions are biogenic volatile organic compounds (BVOC) which, following oxidation in the atmosphere, can condense onto aerosol particles to form secondary organic aerosol (SOA) and significantly modify the particles' properties. In accordance with the expected positive temperature dependence of BVOC emissions, several previous studies have shown that some aerosol properties, such as mass concentration and ability to act as cloud condensation nuclei (CCN), also correlate positively with temperature at many forested sites. There is conflicting evidence as to whether the aerosol direct effects have a temperature dependence due to increased BVOC emissions. The main objective of this study is to investigate the causes of the observed effect of increasing temperatures on the aerosol direct radiative effect, and to provide a quantitative estimate of this effect and of the resulting negative feedback in a warming climate. More specifically, we will investigate the causes of the positive correlation between aerosol optical depth (AOD) and land surface temperature (LST) over southeastern US where biogenic emissions are a significant source of atmospheric particles. In

  10. The Navy Oceanic Vertical Aerosol Model

    DTIC Science & Technology

    1993-12-01

    34windows" exist in the molecular absorption of the electromagnetic energy through which trans- missions in IR communication can take place. In these...the aerosol both scatters and absorbs electromagnetic energy . Of particular interest to the Navy is the role natural marine aerosols play within the...34 \\( )/ •dr12 This technique speeds up the calculations since the integrals can be calculated earlier and their values stored as numbers in a lookup table

  11. A thermoluminescent method for aerosol characterization

    NASA Technical Reports Server (NTRS)

    Long, E. R., Jr.; Rogowski, R. S.

    1976-01-01

    A thermoluminescent method has been used to study the interactions of aerosols with ozone. The preliminary results show that ozone reacts with many compounds found in aerosols, and that the thermoluminescence curves obtained from ozonated aerosols are characteristic of the aerosol. The results suggest several important applications of the thermoluminescent method: development of a detector for identification of effluent sources; a sensitive experimental tool for study of heterogeneous chemistry; evaluation of importance of aerosols in atmospheric chemistry; and study of formation of toxic, electronically excited species in airborne particles.

  12. Toward Creating A Global Retrospective Climatology of Aerosol Properties

    NASA Technical Reports Server (NTRS)

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

    2000-01-01

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

  13. Aerosol and monsoon climate interactions over Asia: AEROSOL AND MONSOON CLIMATE INTERACTIONS

    SciTech Connect

    Li, Zhanqing; Lau, W. K. -M.; Ramanathan, V.; Wu, G.; Ding, Y.; Manoj, M. G.; Liu, J.; Qian, Y.; Li, J.; Zhou, T.; Fan, J.; Rosenfeld, D.; Ming, Y.; Wang, Y.; Huang, J.; Wang, B.; Xu, X.; Lee, S. -S.; Cribb, M.; Zhang, F.; Yang, X.; Zhao, C.; Takemura, T.; Wang, K.; Xia, X.; Yin, Y.; Zhang, H.; Guo, J.; Zhai, P. M.; Sugimoto, N.; Babu, S. S.; Brasseur, G. P.

    2016-11-15

    Asian monsoons and aerosols have been studied extensively which are intertwined in influencing the climate of Asia. This paper provides a comprehensive review of ample studies on Asian aerosol, monsoon and their interactions. The region is the primary source of aerosol emissions of varies species, influenced by distinct weather and climatic regimes. On continental scale, aerosols reduce surface insolation and weaken the land-ocean thermal contrast, thus inhibiting the development of monsoons. Locally, aerosol radiative effects alter the thermodynamic stability and convective potential of the lower atmosphere leading to reduced temperatures, increased atmospheric stability, and weakened wind and atmospheric circulation. The atmospheric thermodynamic state may also be altered by the aerosol serving as cloud condensation nuclei or ice nuclei. Many mechanisms have been put forth regarding how aerosols modulate the amplitude, frequency, intensity, and phase of numerous monsoon climate variables. A wide range of theoretical, observational, and modeling findings on the Asian monsoon, aerosols, and their interactions are synthesized. A new paradigm is proposed on investigating aerosol-monsoon interactions, in which natural aerosols such as desert dust, black carbon from biomass burning, and biogenic aerosols from vegetation are considered integral components of an intrinsic aerosol-monsoon climate system, subject to external forcings of global warming, anthropogenic aerosols, and land use and change. Future research on aerosol-monsoon interactions calls for an integrated approach and international collaborations based on long-term sustained observations, process measurements, and improved models, as well as using observations to constrain model simulations and projections.

  14. Externally tuned vibration absorber

    DOEpatents

    Vincent, Ronald J.

    1987-09-22

    A vibration absorber unit or units are mounted on the exterior housing of a hydraulic drive system of the type that is powered from a pressure wave generated, e.g., by a Stirling engine. The hydraulic drive system employs a piston which is hydraulically driven to oscillate in a direction perpendicular to the axis of the hydraulic drive system. The vibration absorbers each include a spring or other resilient member having one side affixed to the housing and another side to which an absorber mass is affixed. In a preferred embodiment, a pair of vibration absorbers is employed, each absorber being formed of a pair of leaf spring assemblies, between which the absorber mass is suspended.

  15. Shock absorber control system

    SciTech Connect

    Nakano, Y.; Ohira, M.; Ushida, M.; Miyagawa, T.; Shimodaira, T.

    1987-01-13

    A shock absorber control system is described for controlling a dampening force of a shock absorber of a vehicle comprising: setting means for setting a desired dampening force changeable within a predetermined range; drive means for driving the shock absorber to change the dampening force of the shock absorber linearly; control means for controlling the drive means in accordance with the desired dampening force when the setting of the desired dampening force has been changed; detecting means for detecting an actual dampening force of the shock absorber; and correcting means for correcting the dampening force of the shock absorber by controlling the drive means in accordance with a difference between the desired dampening force and the detected actual dampening force.

  16. CPCs with segmented absorbers

    SciTech Connect

    Keita, M.; Robertson, H.S. )

    1991-01-01

    One of the most promising means of improving the performance of solar thermal collectors is to reduce the energy lost by the hot absorber. One way to do this, not currently part of the technology, is to recognize that since the absorber is usually not irradiated uniformly, it is therefore possible to construct an absorber of thermally isolated segments, circulate the fluid in sequence from low to high irradiance segments, and reduce loss by improving effective concentration. This procedure works even for ideal concentrators, without violating Winston's theorem. Two equivalent CPC collectors with single and segmented absorber were constructed and compared under actual operating conditions. The results showed that the daily thermal efficiency of the collector with segmented absorber is higher (about 13%) than that of the collector with nonsegmented absorber.

  17. Methods for absorbing neutrons

    DOEpatents

    Guillen, Donna P [Idaho Falls, ID; Longhurst, Glen R [Idaho Falls, ID; Porter, Douglas L [Idaho Falls, ID; Parry, James R [Idaho Falls, ID

    2012-07-24

    A conduction cooled neutron absorber may include a metal matrix composite that comprises a metal having a thermal neutron cross-section of at least about 50 barns and a metal having a thermal conductivity of at least about 1 W/cmK. Apparatus for providing a neutron flux having a high fast-to-thermal neutron ratio may include a source of neutrons that produces fast neutrons and thermal neutrons. A neutron absorber positioned adjacent the neutron source absorbs at least some of the thermal neutrons so that a region adjacent the neutron absorber has a fast-to-thermal neutron ratio of at least about 15. A coolant in thermal contact with the neutron absorber removes heat from the neutron absorber.

  18. Remote Sensing of Aerosol and Non-Aerosol Absorption

    NASA Technical Reports Server (NTRS)

    Kaufman, Y. J.; Dubovik, O.; Holben, B. N.; Remer, L. A.; Tanre, D.; Lau, William K. M. (Technical Monitor)

    2001-01-01

    Remote sensing of aerosol from the new satellite instruments (e.g. MODIS from Terra) and ground based radiometers (e.g. the AERONET) provides the opportunity to measure the absorption characteristics of the ambient undisturbed aerosol in the entire atmospheric column. For example Landsat and AERONET data are used to measure spectral absorption of sunlight by dust from West Africa. Both Application of the Landsat and AERONET data demonstrate that Saharan dust absorption of solar radiation is several times smaller than the current international standards. This is due to difficulties of measuring dust absorption in situ, and due to the often contamination of dust properties by the presence of air pollution or smoke. We use the remotely sensed aerosol absorption properties described by the spectral sin le scattering albedo, together with statistics of the monthly optical thickness for the fine and coarse aerosol derived from the MODIS data. The result is an estimate of the flux of solar radiation absorbed by the aerosol layer in different regions around the globe where aerosol is prevalent. If this aerosol forcing through absorption is not included in global circulation models, it may be interpreted as anomalous absorption in these regions. In a preliminary exercise we also use the absorption measurements by AERONET, to derive the non-aerosol absorption of the atmosphere in cloud free conditions. The results are obtained for the atmospheric windows: 0.44 microns, 0.66 microns, 0.86 microns and 1.05 microns. In all the locations over the land and ocean that were tested no anomalous absorption in these wavelengths, was found within absorption optical thickness of +/- 0.005.

  19. Aerosol Climate Time Series Evaluation In ESA Aerosol_cci

    NASA Astrophysics Data System (ADS)

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

    2015-12-01

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

  20. Using OMI Observations to Measure Aerosol Absorption of Biomass Burning Aerosols Above Clouds

    NASA Technical Reports Server (NTRS)

    Torres, Omar; Bhartia, P. K.; Jethva, Hiren

    2011-01-01

    The presence of absorbing aerosol layers above clouds is unambiguously detected by the TOMS/OMI UV Aerosol Index (AI) that uses satellite observations at two near-UV channels. A sensitivity study using radiative transfer calculations shows that the AI signal of resulting from the presence of aerosols above clouds is mainly driven by the aerosol absorption optical depth and the optical depth of the underlying cloud. Based on these results, an inversion algorithm has been developed to retrieve the aerosol optical depth (AOD) of aerosol layers above clouds. In this presentation we will discuss the sensitivity analysis, describe the retrieval approach, and present results of applications of the retrieval method to OMI observations over the South Atlantic Ocean. Preliminary error analyses, to be discussed, indicate that the AOD can be underestimated (up to -30%) or overestimated (up to 60%) depending on algorithmic assumptions.

  1. Aerosol in the Pacific troposphere

    NASA Technical Reports Server (NTRS)

    Clarke, Antony D.

    1989-01-01

    The use of near real-time optical techniques is emphasized for the measurement of mid-tropospheric aerosol over the Central Pacific. The primary focus is on measurement of the aerosol size distribution over the range of particle diameters from 0.15 to 5.0 microns that are essential for modeling CO2 backscatter values in support of the laser atmospheric wind sounder (LAWS) program. The measurement system employs a LAS-X (Laser Aerosol Spectrometer-PMS, Boulder, CO) with a custom 256 channel pulse height analyzer and software for detailed measurement and analysis of aerosol size distributions. A thermal preheater system (Thermo Optic Aerosol Descriminator (TOAD) conditions the aerosol in a manner that allows the discrimination of the size distribution of individual aerosol components such as sulfuric acid, sulfates and refractory species. This allows assessment of the relative contribution of each component to the BCO2 signal. This is necessary since the different components have different sources, exhibit independent variability and provide different BCO2 signals for a given mass and particle size. Field activities involve experiments designed to examine both temporal and spatial variability of these aerosol components from ground based and aircraft platforms.

  2. Inferring Aerosol Angstrom Absorption Exponent using satellite observations

    NASA Astrophysics Data System (ADS)

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

    2013-12-01

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

  3. AEROSOL, CLOUDS, AND CLIMATE CHANGE

    SciTech Connect

    SCHWARTZ, S.E.

    2005-09-01

    Earth's climate is thought to be quite sensitive to changes in radiative fluxes that are quite small in absolute magnitude, a few watts per square meter, and in relation to these fluxes in the natural climate. Atmospheric aerosol particles exert influence on climate directly, by scattering and absorbing radiation, and indirectly by modifying the microphysical properties of clouds and in turn their radiative effects and hydrology. The forcing of climate change by these indirect effects is thought to be quite substantial relative to forcing by incremental concentrations of greenhouse gases, but highly uncertain. Quantification of aerosol indirect forcing by satellite- or ground-based remote sensing has proved quite difficult in view of inherent large variation in the pertinent observables such as cloud optical depth, which is controlled mainly by liquid water path and only secondarily by aerosols. Limited work has shown instances of large magnitude of aerosol indirect forcing, with local instantaneous forcing upwards of 50 W m{sup 66}-2. Ultimately it will be necessary to represent aerosol indirect effects in climate models to accurately identify the anthropogenic forcing at present and over secular time and to assess the influence of this forcing in the context of other forcings of climate change. While the elements of aerosol processes that must be represented in models describing the evolution and properties of aerosol particles that serve as cloud condensation particles are known, many important components of these processes remain to be understood and to be represented in models, and the models evaluated against observation, before such model-based representations can confidently be used to represent aerosol indirect effects in climate models.

  4. ENCAPSULATED AEROSOLS

    DTIC Science & Technology

    acetate, polymerized rapidly and produced some polymer film encapsulation of the aerosol droplets. A two-stage microcapsule generator was designed...encapsulating material, the generator also produced microcapsules of dibutyl phosphite in polyethylene, nitrocellulose, and natural rubber.

  5. A Wintertime Aerosol Model for the Ganga Basin, Northern India

    NASA Astrophysics Data System (ADS)

    Dey, S.; Tripathi, S. N.

    2006-05-01

    An aerosol model has been developed using mass size distributions of various chemical components measured at Kanpur (an urban location in the Ganga basin, GB, in Northern India) and applied to estimate the radiative effects of the aerosols over the entire GB during the winter season for the first time. The number size distribution of various species was derived from the measured mass concentration and the optical properties were calculated using OPAC model. The anthropogenic contribution to the total extinction was found to be more than 90%. The relative contribution of various species to the aerosol optical depth (AOD) at 0.5 μm are in the following order, (NH2)2SO4 (AS, 37%), nitrate (N, 28%), other salts (S, mainly NaCl and KCl, 19%), dust (9%) and black carbon, BC (7%). Contribution of AS, N, S to the observed AOD decreases with wavelength and that of dust increases with wavelength, whereas, BC contribution remains almost same. The extinction coefficient strongly depends on the relative humidity (RH), as the scattering by fine mode fraction (contributing 88% to the total extinction) is enhanced at high ambient RH. The spectral variation of absorption coefficient indicates that the most likely source of BC (as BC is the dominant absorbing species) in this region is fossil- fuel. The spectral variation of single scattering albedo (SSA) in the fine and coarse mode fractions and that of asymmetry parameter suggests that the internal mixing is more likely scenario, although the possibility of external mixing can not be ruled out. If the RH is lowered by ~20%, BC contribution to the AOD increases by ~3.5%, which implies that the RH is a strong controlling factor of the aerosol forcing. The mean shortwave clear sky top of the atmosphere (TOA) and surface forcing over Kanpur are -13±3 and -43±8 W m-2. Extending the TOA and surface efficiency over the entire GB, the mean TOA and surface forcing become -9±3 and -25±10 W m-2. This results in high atmospheric

  6. Uptake and metabolism of benzo(a)pyrene absorbed to sediment by the freshwater invertebrate species Chironomus riparius and Sphaerium corneum

    SciTech Connect

    Borchert, J.; Karbe, L.; Westendorf, J.

    1997-01-01

    The polyaromatic hydrocarbon (PAH) Benzo(a)pyrene (BP) is a widespread contaminant, which is known to be carcinogenic in mammals after ic activation. BP is released into the environment and the water as a by-product of combustion of fossil and recent material (fuel, wood) in industry, traffic and households and is also released by natural sources. Most of the PAHs are highly lipophilic and therefore bound to humic substances, dissolved macromolecules and particulate matter which are at least deposited in the aquatic sediments. The BP concentrations in sediments of pristine waters do normally not exceed 1 {mu}g/g dry weight (dw). In polluted waters of industrial areas, the BP concentration may increase up to 100 {mu}g/g dw. The risk for environmental health caused by such sediment bound PAHs can be assessed by using BP as a model substance. One aim of this study was to investigate if the sediment bound BP is bioavailable to sediment dwelling organisms. For this purpose we examined the uptake of sediment bound BP. The metabolism of PAHs in insects has been investigated, however, only little is known about the Phase I and Phase II metabolism in clams, especially in freshwater species. The organisms choosen were two sediment inhabiting invertebrates, the larvae of the midge Chironomus riparius and the European fingernail clam Sphaerium corneum. Also investigated was the question of whether the BP taken up by the test organisms undergoes metabolic activation, since the toxicity of BP is modulated by metabolism. 11 refs., 3 figs., 4 tabs.

  7. Aerosol Microphysics and Radiation Integration

    DTIC Science & Technology

    2016-06-13

    storm activity, and 4) surface and airborne measurements on the west coast of the U.S. indicate the presence of aerosols and dust on the predicted...observables (in situ and satellites) and model quantities such as mass. Aerosol species currently included in the analyses are dust , pollution, biomass...Prediction System ( COAMPS ®). Over the next several years it is the goal of this project to maintain these systems as the world leaders in EO prediction

  8. Advanced neutron absorber materials

    DOEpatents

    Branagan, Daniel J.; Smolik, Galen R.

    2000-01-01

    A neutron absorbing material and method utilizing rare earth elements such as gadolinium, europium and samarium to form metallic glasses and/or noble base nano/microcrystalline materials, the neutron absorbing material having a combination of superior neutron capture cross sections coupled with enhanced resistance to corrosion, oxidation and leaching.

  9. Shortwave and longwave radiative forcings of aerosols depending on the vertical stratification of aerosols and clouds

    NASA Astrophysics Data System (ADS)

    Oikawa, Eiji; Suzuki, Kentaroh; Nakajima, Teruyuki; Nishizawa, Tomoaki

    2017-02-01

    We investigate four scenarios for estimating shortwave (SW) and longwave (LW) direct aerosol radiative forcing (DARF) at the top of atmosphere (TOA) using the global data set of the vertical distributions for aerosols and clouds of CALIPSO and CloudSat Level 2 products. One scenario is clear-sky (cloud-free) condition and three scenarios are cloudy-sky condition: the case that aerosols exists above clouds (AAC case), and the case that aerosols exist below high clouds such as cirrus, but without clouds below the aerosol layers (ABC case), and the case that aerosols are not observed in cloudy-sky condition. In clear-sky and ABC cases, aerosols mainly scatter sunlight and SWDARFs show negative values, except for bright surfaces, such as desert regions and the North and South Poles. In AAC case, aerosols absorb the reflected light from underlying low-level clouds to TOA, so that SWDARF at TOA shows positive value. Mineral dust absorbs the Earth's radiation and LWDARF indicates strong positive over Saharan and Arabian deserts. The global mean values of SW plus LW DARFs are -2.77, -0.77, and -1.40 Wm-2 under clear-sky, cloudy-sky, and all-sky conditions.

  10. Multispectral metamaterial absorber.

    PubMed

    Grant, J; McCrindle, I J H; Li, C; Cumming, D R S

    2014-03-01

    We present the simulation, implementation, and measurement of a multispectral metamaterial absorber (MSMMA) and show that we can realize a simple absorber structure that operates in the mid-IR and terahertz (THz) bands. By embedding an IR metamaterial absorber layer into a standard THz metamaterial absorber stack, a narrowband resonance is induced at a wavelength of 4.3 μm. This resonance is in addition to the THz metamaterial absorption resonance at 109 μm (2.75 THz). We demonstrate the inherent scalability and versatility of our MSMMA by describing a second device whereby the MM-induced IR absorption peak frequency is tuned by varying the IR absorber geometry. Such a MSMMA could be coupled with a suitable sensor and formed into a focal plane array, enabling multispectral imaging.

  11. Synergic use of TOMS and Aeronet Observations for Characterization of Aerosol Absorption

    NASA Technical Reports Server (NTRS)

    Torres, O.; Bhartia, P. K.; Dubovik, O.; Holben, B.; Siniuk, A.

    2003-01-01

    The role of aerosol absorption on the radiative transfer balance of the earth-atmosphere system is one of the largest sources of uncertainty in the analysis of global climate change. Global measurements of aerosol single scattering albedo are, therefore, necessary to properly assess the radiative forcing effect of aerosols. Remote sensing of aerosol absorption is currently carried out using both ground (Aerosol Robotic Network) and space (Total Ozone Mapping Spectrometer) based observations. The satellite technique uses measurements of backscattered near ultraviolet radiation. Carbonaceous aerosols, resulting from the combustion of biomass, are one of the most predominant absorbing aerosol types in the atmosphere. In this presentation, TOMS and AERONET retrievals of single scattering albedo of carbonaceous aerosols, are compared for different environmental conditions: agriculture related biomass burning in South America and Africa and peat fires in Eastern Europe. The AERONET and TOMS derived aerosol absorption information are in good quantitative agreement. The most absorbing smoke is detected over the African Savanna. Aerosol absorption over the Brazilian rain forest is less absorbing. Absorption by aerosol particles resulting from peat fires in Eastern Europe is weaker than the absorption measured in Africa and South America. This analysis shows that the near UV satellite method of aerosol absorption characterization has the sensitivity to distinguish different levels of aerosol absorption. The analysis of the combined AERONET-TOMS observations shows a high degree of synergy between satellite and ground based observations.

  12. Using the OMI Aerosol Index and Absorption Aerosol Optical Depth to evaluate the NASA MERRA Aerosol Reanalysis

    NASA Astrophysics Data System (ADS)

    Buchard, V.; da Silva, A. M.; Colarco, P. R.; Darmenov, A.; Randles, C. A.; Govindaraju, R.; Torres, O.; Campbell, J.; Spurr, R.

    2014-12-01

    A radiative transfer interface has been developed to simulate the UV Aerosol Index (AI) from the NASA Goddard Earth Observing System version 5 (GEOS-5) aerosol assimilated fields. The purpose of this work is to use the AI and Aerosol Absorption Optical Depth (AAOD) derived from the Ozone Monitoring Instrument (OMI) measurements as independent validation for the Modern Era Retrospective analysis for Research and Applications Aerosol Reanalysis (MERRAero). MERRAero is based on a version of the GEOS-5 model that is radiatively coupled to the Goddard Chemistry, Aerosol, Radiation, and Transport (GOCART) aerosol module and includes assimilation of Aerosol Optical Depth (AOD) from the Moderate Resolution Imaging Spectroradiometer (MODIS) sensor. Since AI is dependent on aerosol concentration, optical properties and altitude of the aerosol layer, we make use of complementary observations to fully diagnose the model, including AOD from the Multi-angle Imaging SpectroRadiometer (MISR), aerosol retrievals from the Aerosol Robotic Network (AERONET) and attenuated backscatter coefficients from the Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observation (CALIPSO) mission to ascertain potential misplacement of plume height by the model. By sampling dust, biomass burning and pollution events in 2007 we have compared model produced AI and AAOD with the corresponding OMI products, identifying regions where the model representation of absorbing aerosols was deficient. As a result of this study over the Saharan dust region, we have obtained a new set of dust aerosol optical properties that retains consistency with the MODIS AOD data that were assimilated, while resulting in better agreement with aerosol absorption measurements from OMI. The analysis conducted over the South African and South American biomass burning regions indicates that revising the spectrally-dependent aerosol absorption properties in the near-UV region improves the modeled-observed AI comparisons

  13. Using the OMI aerosol index and absorption aerosol optical depth to evaluate the NASA MERRA Aerosol Reanalysis

    NASA Astrophysics Data System (ADS)

    Buchard, V.; da Silva, A. M.; Colarco, P. R.; Darmenov, A.; Randles, C. A.; Govindaraju, R.; Torres, O.; Campbell, J.; Spurr, R.

    2015-05-01

    A radiative transfer interface has been developed to simulate the UV aerosol index (AI) from the NASA Goddard Earth Observing System version 5 (GEOS-5) aerosol assimilated fields. The purpose of this work is to use the AI and aerosol absorption optical depth (AAOD) derived from the Ozone Monitoring Instrument (OMI) measurements as independent validation for the Modern Era Retrospective analysis for Research and Applications Aerosol Reanalysis (MERRAero). MERRAero is based on a version of the GEOS-5 model that is radiatively coupled to the Goddard Chemistry, Aerosol, Radiation, and Transport (GOCART) aerosol module and includes assimilation of aerosol optical depth (AOD) from the Moderate Resolution Imaging Spectroradiometer (MODIS) sensor. Since AI is dependent on aerosol concentration, optical properties and altitude of the aerosol layer, we make use of complementary observations to fully diagnose the model, including AOD from the Multi-angle Imaging SpectroRadiometer (MISR), aerosol retrievals from the AErosol RObotic NETwork (AERONET) and attenuated backscatter coefficients from the Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observation (CALIPSO) mission to ascertain potential misplacement of plume height by the model. By sampling dust, biomass burning and pollution events in 2007 we have compared model-produced AI and AAOD with the corresponding OMI products, identifying regions where the model representation of absorbing aerosols was deficient. As a result of this study over the Saharan dust region, we have obtained a new set of dust aerosol optical properties that retains consistency with the MODIS AOD data that were assimilated, while resulting in better agreement with aerosol absorption measurements from OMI. The analysis conducted over the southern African and South American biomass burning regions indicates that revising the spectrally dependent aerosol absorption properties in the near-UV region improves the modeled-observed AI comparisons

  14. Internal absorber solar collector

    DOEpatents

    Sletten, Carlyle J.; Herskovitz, Sheldon B.; Holt, F. S.; Sletten, E. J.

    1981-01-01

    Thin solar collecting panels are described made from arrays of small rod collectors consisting of a refracting dielectric rod lens with an absorber imbedded within it and a reflecting mirror coated on the back side of the dielectric rod. Non-tracking collector panels on vertical walls or roof tops receive approximately 90% of solar radiation within an acceptance zone 60.degree. in elevation angle by 120.degree. or more in the azimuth sectors with a collector concentration ratio of approximately 3.0. Miniaturized construction of the circular dielectric rods with internal absorbers reduces the weight per area of glass, plastic and metal used in the collector panels. No external parts or insulation are needed as heat losses are low due to partial vacuum or low conductivity gas surrounding heated portions of the collector. The miniature internal absorbers are generally made of solid copper with black selective surface and the collected solar heat is extracted at the collector ends by thermal conductivity along the absorber rods. Heat is removed from end fittings by use of liquid circulants. Several alternate constructions are provided for simplifying collector panel fabrication and for preventing the thermal expansion and contraction of the heated absorber or circulant tubes from damaging vacuum seals. In a modified version of the internal absorber collector, oil with temperature dependent viscosity is pumped through a segmented absorber which is now composed of closely spaced insulated metal tubes. In this way the circulant is automatically diverted through heated portions of the absorber giving higher collector concentration ratios than theoretically possible for an unsegmented absorber.

  15. Lipid-absorbing Polymers

    NASA Technical Reports Server (NTRS)

    Marsh, H. E., Jr.; Wallace, C. J.

    1973-01-01

    The removal of bile acids and cholesterol by polymeric absorption is discussed in terms of micelle-polymer interaction. The results obtained with a polymer composed of 75 parts PEO and 25 parts PB plus curing ingredients show an absorption of 305 to 309%, based on original polymer weight. Particle size effects on absorption rate are analyzed. It is concluded that crosslinked polyethylene oxide polymers will absorb water, crosslinked polybutadiene polymers will absorb lipids; neither polymer will absorb appreciable amounts of lipids from micellar solutions of lipids in water.

  16. Electromagnetic power absorber

    NASA Technical Reports Server (NTRS)

    Iwasaki, R. S. (Inventor)

    1979-01-01

    A structure is presented with a surface portion of dielectric material which passes electromagnetic radiation and with a portion below the surface which includes material that absorbs the radiation, the face of the structure being formed with numerous steep ridges. The steepness of the dielectric material results in a high proportion of the electromagnetic energy passing through the surface for absorption by the absorbing material under the surface. A backing of aluminum or other highly heat-conductive and reflective material lies under the face and has very steep protuberances supporting the absorbing and dielectric materials.

  17. Aerosols, light, and water: Measurements of aerosol optical properties at different relative humidities

    NASA Astrophysics Data System (ADS)

    Orozco, Daniel

    The Earth's atmosphere is composed of a large number of different gases as well as tiny suspended particles, both in solid and liquid state. These tiny particles, called atmospheric aerosols, have an immense impact on our health and on our global climate. Atmospheric aerosols influence the Earth's radiation budget both directly and indirectly. In the direct effect, aerosols scatter and absorb sunlight changing the radiative balance of the Earth-atmosphere system. Aerosols indirectly influence the Earth's radiation budget by modifying the microphysical and radiative properties of clouds as well as their water content and lifetime. In ambient conditions, aerosol particles experience hygroscopic growth due to the influence of relative humidity (RH), scattering more light than when the particles are dry. The quantitative knowledge of the RH effect and its influence on the light scattering coefficient and, in particular, on the phase function and polarization of aerosol particles is of substantial importance when comparing ground based observations with other optical aerosol measurements techniques such satellite and sunphotometric retrievals of aerosol optical depth and their inversions. This dissertation presents the aerosol hygroscopicity experiment investigated using a novel dryer-humidifier system, coupled to a TSI-3563 nephelometer, to obtain the light scattering coefficient (sp) as a function of relative humidity (RH) in hydration and dehydration modes. The measurements were performed in Porterville, CA (Jan 10-Feb 6, 2013), Baltimore, MD (Jul 3-30, 2013), and Golden, CO (Jul 12-Aug 10, 2014). Observations in Porterville and Golden were part of the NASA-sponsored DISCOVER-AQ project. The measured sp under varying RH in the three sites was combined with ground aerosol extinction, PM2:5mass concentrations, particle composition measurements, and compared with airborne observations performed during campaigns. The enhancement factor, f(RH), defined as the ratio of sp

  18. Retrieval of UV Aerosol Index using backscattered monochromatic radiance measured by GOSAT CAI

    NASA Astrophysics Data System (ADS)

    Go, S.; Kim, J.; KIM, M.; Park, S. S.

    2014-12-01

    UV Aerosol Index(AI) using backscattered radiance at a single channel has been retrieved. In the current UV AI algorithm, two UV channels are used to contrast the absorbing aerosol loaded atmosphere to Rayleigh scattering condition. There have been needs to retrieve information of absorbing aerosol from a single UV channel, such as GOSAT CAI. 30-day minimum composite method, however, makes the process possible to construct the condition with the use of only single UV channel. Also, absorption by aerosol changes with respect to AOD and wavelength for different aerosol types. Therefore, single channel aerosol index(SAI) can detect absorbing aerosol qualitatively. Correlation coefficient of SAI to current UV AI indicate significant value, showing possibility of detecting highly absorbing aerosols. The application of a cloud screening makes the presence of absorbing aerosols even more clear. Radiative transfer calculations using VLIDORT were performed to test the sensitivity of SAI and UV AI to aerosol optical properties, showing that highly absorbing aerosol results in meaningful SAI. Results from dust case study in East Asia show reasonable performance of SAI for the region with single scattering albedo below 0.90. This study concludes with a comparison of SAI from GOSAT lv.1b data to OMI UVAI data, where reasonable agreement and low false detection was found for dust cases in East Asia. The SAI value of -0.2 to 0.0 from GOSAT-CAI was comparable to OMI dust threshold value of 0.7. These findings corroborate the suitability of SAI as a for detecting absorbing aerosols for satellite instrument with a single UV channel.

  19. Spectrophotometry of Thin Films of Light-Absorbing Particles.

    PubMed

    Binks, Bernard P; Fletcher, Paul D I; Johnson, Andrew J; Marinopoulos, Ioannis; Crowther, Jonathan M; Thompson, Michael A

    2017-04-06

    Thin films of dispersions of light-absorbing solid particles or emulsions containing a light-absorbing solute all have a nonuniform distribution of light-absorbing species throughout the sample volume. This results in nonuniform light absorption over the illuminated area, which causes the optical absorbance, as measured using a conventional specular UV-vis spectrophotometer, to deviate from the Beer-Lambert relationship. We have developed a theoretical model to account for the absorbance properties of such films, which are shown to depend on the size and volume fraction of the light-absorbing particles plus other sample variables. We have compared model predictions with measured spectra for samples consisting of emulsions containing a dissolved light-absorbing solute. Using no adjustable parameters, the model successfully predicts the behavior of nonuniform, light-absorbing emulsion films with varying values of droplet size, volume fraction, and other parameters.

  20. Effects of Aerosols over the Indian Ocean

    NASA Technical Reports Server (NTRS)

    2002-01-01

    Aerosols that contain black carbon both absorb and reflect incoming sunlight. Even as these atmospheric particles reduce the amount of sunlight reaching the surface, they increase the amount of solar energy absorbed in the atmosphere, thus making it possible to both cool the surface and warm the atmosphere. The images above show satellite measurements of the region studied during the Indian Ocean Experiment (INDOEX)a vast region spanning the Arabian Sea and Bay of Bengal (west to east), and from the foot of the Himalayan Mountains, across the Indian subcontinent to the southern Indian Ocean (north to south). The Aerosol images show aerosol pollution (brownish pixels) in the lower atmosphere over the INDOEX study area, as measured by the Moderate-resolution Imaging Spectroradiometer (MODIS) aboard Terra. These were composited from March 14-21, 2001. The Albedo images show the total solar energy reflected back to space, as measured by Clouds and Earth's Radiant Energy System (CERES) aboard Terra. White pixels show high values, greens are intermediate values, and blues are low. Note how the aerosols, particularly over the ocean, increase the amount of energy reflected back to space. The Atmospheric Warming images show the absorption of the black carbon aerosols in the atmosphere. Where the aerosols are most dense, the absorption is highest. Red pixels indicate the highest levels of absorption, blues are low. The Surface Cooling images show that the aerosol particles reduce the amount of sunlight reaching the surface. Dark pixels show where the aerosols exert their cooling influence on the surface (or a high magnitude of negative radiative forcing). The bright pixels show where there is much less aerosol pollution and the incoming sunlight is relatively unaffected.

  1. "Smart" Electromechanical Shock Absorber

    NASA Technical Reports Server (NTRS)

    Stokes, Lebarian; Glenn, Dean C.; Carroll, Monty B.

    1989-01-01

    Shock-absorbing apparatus includes electromechanical actuator and digital feedback control circuitry rather than springs and hydraulic damping as in conventional shock absorbers. Device not subject to leakage and requires little or no maintenance. Attenuator parameters adjusted in response to sensory feedback and predictive algorithms to obtain desired damping characteristic. Device programmed to decelerate slowly approaching vehicle or other large object according to prescribed damping characteristic.

  2. Water absorption by secondary organic aerosol and its effect on inorganic aerosol behavior

    SciTech Connect

    Ansari, A.S.; Pandis, S.N.

    2000-01-01

    The hygroscopic nature of atmospheric aerosol has generally been associated with its inorganic fraction. In this study, a group contribution method is used to predict the water absorption of secondary organic aerosol (SOA). Compared against growth measurements of mixed inorganic-organic particles, this method appears to provide a first-order approximation in predicting SOA water absorption. The growth of common SOA species is predicted to be significantly less than common atmospheric inorganic salts such as (NH{sub 4}){sub 2}SO{sub 4} and NaCl. Using this group contribution method as a tool in predicting SOA water absorption, an integrated modeling approach is developed combining available SOA and inorganic aerosol models to predict overall aerosol behavior. The effect of SOA on water absorption and nitrate partitioning between the gas and aerosol phases is determined. On average, it appears that SOA accounts for approximately 7% of total aerosol water and increases aerosol nitrate concentrations by approximately 10%. At high relative humidity and low SOA mass fractions, the role of SOA in nitrate partitioning and its contribution to total aerosol water is negligible. However, the water absorption of SOA appears to be less sensitive to changes in relative humidity than that of inorganic species, and thus at low relative humidity and high SOA mass fraction concentrations, SOA is predicted to account for approximately 20% of total aerosol water and a 50% increase in aerosol nitrate concentrations. These findings could improve the results of modeling studies where aerosol nitrate has often been underpredicted.

  3. Molecular Characterization of Brown Carbon in Biomass Burning Aerosol Particles

    SciTech Connect

    Lin, Peng; Aiona, Paige K.; Li, Ying; Shiraiwa, Manabu; Laskin, Julia; Nizkorodov, Sergey A.; Laskin, Alexander

    2016-11-01

    Emissions from biomass burning are a significant source of brown carbon (BrC) in the atmosphere. In this study, we investigate the molecular composition of freshly-emitted biomass burning organic aerosol (BBOA) samples collected during test burns of selected biomass fuels: sawgrass, peat, ponderosa pine, and black spruce. We characterize individual BrC chromophores present in these samples using high performance liquid chromatography coupled to a photodiode array detector and a high-resolution mass spectrometer. We demonstrate that both the overall BrC absorption and the chemical composition of light-absorbing compounds depend significantly on the type of biomass fuels and burning conditions. Common BrC chromophores in the selected BBOA samples include nitro-aromatics, polycyclic aromatic hydrocarbon derivatives, and polyphenols spanning a wide range of molecular weights, structures, and light absorption properties. A number of biofuel-specific BrC chromophores are observed, indicating that some of them may be used as potential markers of BrC originating from different biomass burning sources. On average, ~50% of the light absorption above 300 nm can be attributed to a limited number of strong BrC chromophores, which may serve as representative light-absorbing species for studying atmospheric processing of BrC aerosol. The absorption coefficients of BBOA are affected by solar photolysis. Specifically, under typical atmospheric conditions, the 300 nm absorbance decays with a half-life of 16 hours. A “molecular corridors” analysis of the BBOA volatility distribution suggests that many BrC compounds in the fresh BBOA have low volatility (<1 g m-1) and will be retained in the particle phase under atmospherically relevant conditions.

  4. Impact of anthropogenic aerosols on Indian summer monsoon

    SciTech Connect

    Wang, Chien; Kim, Dongchul; Ekman, Annica; Barth, Mary; Rasch, Philip J.

    2009-11-05

    Using an interactive aerosol-climate model we find that absorbing anthropogenic aerosols, whether coexisting with scattering aerosols or not, can significantly affect the Indian summer monsoon system. We also show that the influence is reflected in a perturbation to the moist static energy in the sub-cloud layer, initiated as a heating by absorbing aerosols to the planetary boundary layer. The perturbation appears mostly over land, extending from just north of the Arabian Sea to northern India along the southern slope of the Tibetan Plateau. As a result, during the summer monsoon season, modeled convective precipitation experiences a clear northward shift, coincidently in agreement with observed monsoon precipitation changes in recent decades particularly during the onset season. We demonstrate that the sub-cloud layer moist static energy is a useful quantity for determining the impact of aerosols on the northward extent and to a certain degree the strength of monsoon convection.

  5. Reference values for the production of the aqueous fraction of the tear film measured by the standardized endodontic absorbent paper point test in different exotic and laboratory animal species.

    PubMed

    Lange, Rogério R; Lima, Leandro; Przydzimirski, Andreise C; Montiani-Ferreira, Fabiano

    2014-01-01

    The aqueous fraction of the tear film and the horizontal palpebral fissure length (HPFL) were measured in exotic and laboratory animals, specifically saffron finches (Sicalis flaveola), chestnut-bellied seed-finches (Sporophila angolensis), red-eared sliders (Trachemys scripta elegans), rats (Rattus norvegicus) and mice (Mus musculus). These species possess small eyes making it difficult to perform the typical Schirmer tear test. Measurement of the aqueous fraction of the tear was performed using the standardized endodontic absorbent paper point tear test (PPTT), accomplished with manual restraint by a single operator. The following results were obtained: saffron finches (n = 42)-HPFL (4.46 ± 0.09 mm) and PPTT (5.10 ± 0.26 mm); chestnut-bellied seed-finches (n = 38)-HPFL (4.77 ± 0.05 mm) and PPTT (4.11 ± 0.34 mm); red-eared sliders (n = 56)-HPFL (8.59 ± 0.08 mm) and PPTT (8.79 ± 0.38 mm); rats (n = 60)-HPFL (6.45 ± 0.09 mm) and PTT (6.18 ± 2.06 mm); and mice (n = 22)-HPFL (3.59 ± 0.27 mm) and PPTT (4.39 ± 1.45 mm).

  6. A novel Aerosol-Into-Liquid Collector for online measurements of trace metal and elements in ambient particulate matter (PM)

    NASA Astrophysics Data System (ADS)

    Wang, Dongbin; Shafer, Martin; Schauer, James; Sioutas, Constantinos

    2015-04-01

    A novel monitor for online, in-situ measurement of several important metal species (i.e. Fe, Mn and Cr) in ambient fine and ultrafine particulate matter (PM) is developed based on a recent published high flow rate Aerosol-Into-Liquid Collector. This Aerosol-Into-Liquid Collector collects particles directly as highly concentrated slurry samples, and the concentrations of target metals in slurry samples are subsequently determined in a Micro Volume Flow Cell (MVFC) coupled with absorbance spectrophotometry to detect colored complexes coming from the reactions between target metals and specific reagents. Laboratory tests are conducted to evaluate the performance of the MVFC-absorbance system. The calibration curves of the system are determined using standard solutions prepared by serial dilution. As part of the evaluation, the effects of reaction time, reagent amount and interference on the system are also evaluated. Field evaluations of the online monitor will be performed to validate the ability of this new online sampler in near-continuous collection and measurements. Both laboratory and field evaluations of the novel monitor will indicate that it is an effective and valuable technology for PM collection and characterization of important metal species in ambient aerosols.

  7. Synergetic formation of secondary inorganic and organic aerosol: effect of SO2 and NH3 on particle formation and growth

    NASA Astrophysics Data System (ADS)

    Chu, Biwu; Zhang, Xiao; Liu, Yongchun; He, Hong; Sun, Yele; Jiang, Jingkun; Li, Junhua; Hao, Jiming

    2016-11-01

    The effects of SO2 and NH3 on secondary organic aerosol formation have rarely been investigated together, while the interactive effects between inorganic and organic species under highly complex pollution conditions remain uncertain. Here we studied the effects of SO2 and NH3 on secondary aerosol formation in the photooxidation system of toluene/NOx in the presence or absence of Al2O3 seed aerosols in a 2 m3 smog chamber. The presence of SO2 increased new particle formation and particle growth significantly, regardless of whether NH3 was present. Sulfate, organic aerosol, nitrate, and ammonium were all found to increase linearly with increasing SO2 concentrations. The increases in these four species were more obvious under NH3-rich conditions, and the generation of nitrate, ammonium, and organic aerosol increased more significantly than sulfate with respect to SO2 concentration, while sulfate was the most sensitive species under NH3-poor conditions. The synergistic effects between SO2 and NH3 in the heterogeneous process contributed greatly to secondary aerosol formation. Specifically, the generation of NH4NO3 was found to be highly dependent on the surface area concentration of suspended particles, and increased most significantly with SO2 concentration among the four species under NH3-rich conditions. Meanwhile, the absorbed NH3 might provide a liquid surface layer for the absorption and subsequent reaction of SO2 and organic products and, therefore, enhance sulfate and secondary organic aerosol (SOA) formation. This effect mainly occurred in the heterogeneous process and resulted in a significantly higher growth rate of seed aerosols compared to without NH3. By applying positive matrix factorisation (PMF) analysis to the AMS data, two factors were identified for the generated SOA. One factor, assigned to less-oxidised organic aerosol and some oligomers, increased with increasing SO2 under NH3-poor conditions, mainly due to the well-known acid catalytic effect of

  8. Effects of aerosol organics on cloud condensation nucleus (CCN) concentration and first indirect aerosol effect

    SciTech Connect

    Wang, J. X.; Lee, Y.- N.; Daum, Peter H.; Jayne, John T.; Alexander, M. L.

    2008-11-03

    Abstract. Aerosol microphysics, chemical composition, and CCN properties were measured on the Department of Energy Gulfstream-1 aircraft during the Marine Stratus/ Stratocumulus Experiment (MASE) conducted over the coastal waters between Point Reyes National Seashore and Monterey Bay, California, in July 2005. Aerosols measured during MASE included free tropospheric aerosols, marine boundary layer aerosols, and aerosols with high organic concentration within a thin layer above the cloud. Closure analysis was carried out for all three types of aerosols by comparing the measured CCN concentrations at 0.2% supersaturation to those predicted based on size distribution and chemical composition using K¨ohler theory. The effect of aerosol organic species on predicted CCN concentration was examined using a single hygroscopicity parameterization.

  9. Secondary aerosol formation from stress-induced biogenic emissions and possible climate feedbacks

    NASA Astrophysics Data System (ADS)

    Mentel, Th. F.; Kleist, E.; Andres, S.; Dal Maso, M.; Hohaus, T.; Kiendler-Scharr, A.; Rudich, Y.; Springer, M.; Tillmann, R.; Uerlings, R.; Wahner, A.; Wildt, J.

    2013-09-01

    Atmospheric aerosols impact climate by scattering and absorbing solar radiation and by acting as ice and cloud condensation nuclei. Biogenic secondary organic aerosols (BSOAs) comprise an important component of atmospheric aerosols. Biogenic volatile organic compounds (BVOCs) emitted by vegetation are the source of BSOAs. Pathogens and insect attacks, heat waves and droughts can induce stress to plants that may impact their BVOC emissions, and hence the yield and type of formed BSOAs, and possibly their climatic effects. This raises questions of whether stress-induced changes in BSOA formation may attenuate or amplify effects of climate change. In this study we assess the potential impact of stress-induced BVOC emissions on BSOA formation for tree species typical for mixed deciduous and Boreal Eurasian forests. We studied the photochemical BSOA formation for plants infested by aphids in a laboratory setup under well-controlled conditions and applied in addition heat and drought stress. The results indicate that stress conditions substantially modify BSOA formation and yield. Stress-induced emissions of sesquiterpenes, methyl salicylate, and C17-BVOCs increase BSOA yields. Mixtures including these compounds exhibit BSOA yields between 17 and 33%, significantly higher than mixtures containing mainly monoterpenes (4-6% yield). Green leaf volatiles suppress SOA formation, presumably by scavenging OH, similar to isoprene. By classifying emission types, stressors and BSOA formation potential, we discuss possible climatic feedbacks regarding aerosol effects. We conclude that stress situations for plants due to climate change should be considered in climate-vegetation feedback mechanisms.

  10. Secondary aerosol formation from stress-induced biogenic emissions and possible climate feedbacks

    NASA Astrophysics Data System (ADS)

    Mentel, Th. F.; Kleist, E.; Andres, S.; Maso, M. D.; Hohaus, T.; Kiendler-Scharr, A.; Rudich, Y.; Springer, M.; Tillmann, R.; Uerlings, R.; Wahner, A.; Wildt, J.

    2013-03-01

    Atmospheric aerosols impact climate by scattering and absorbing solar radiation and by acting as ice and cloud condensation nuclei. Secondary organic aerosols (SOA) comprise an important component of atmospheric aerosols. Biogenic volatile organic compounds (BVOC) emitted by vegetation are a major source of SOA. Pathogens and insect attacks, heat waves and droughts can induce stress to plants that may impact their BVOC emissions, and hence the yield and type of formed SOA, and possibly their climatic effects. This raises questions whether stress-induced changes in SOA formation may attenuate or amplify effects of climate change. In this study we assess the potential impact of stress-induced BVOC emissions on SOA formation for tree species typical for mixed deciduous and Boreal Eurasian forests. We studied the photochemical SOA formation for infested plants in a laboratory setup under well-controlled conditions and applied in addition heat and drought stress. The results indicate that stress conditions substantially modify SOA formation. While sesquiterpenes, methyl salicylate, and C17-BVOC increase SOA yield, green leaf volatiles suppress SOA formation. By classifying emission types, stressors and SOA formation potential, we propose possible climatic feedbacks regarding aerosol effects. We conclude that stress situations for plants due to climate change should be considered in climate-vegetation feedback mechanisms.

  11. Toxicity of atmospheric aerosols on marine phytoplankton

    PubMed Central

    Paytan, Adina; Mackey, Katherine R. M.; Chen, Ying; Lima, Ivan D.; Doney, Scott C.; Mahowald, Natalie; Labiosa, Rochelle; Post, Anton 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. PMID:19273845

  12. Toxicity of atmospheric aerosols on marine phytoplankton

    USGS Publications Warehouse

    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.

  13. Humidity Dependent Extinction of Clay Aerosols

    NASA Astrophysics Data System (ADS)

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

    2010-12-01

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

  14. Climate impact of biofuels in shipping: global model studies of the aerosol indirect effect.

    PubMed

    Righi, Mattia; Klinger, Carolin; Eyring, Veronika; Hendricks, Johannes; Lauer, Axel; Petzold, Andreas

    2011-04-15

    Aerosol emissions from international shipping are recognized to have a large impact on the Earth's radiation budget, directly by scattering and absorbing solar radiation and indirectly by altering cloud properties. New regulations have recently been approved by the International Maritime Organization (IMO) aiming at progressive reductions of the maximum sulfur content allowed in marine fuels from current 4.5% by mass down to 0.5% in 2020, with more restrictive limits already applied in some coastal regions. In this context, we use a global bottom-up algorithm to calculate geographically resolved emission inventories of gaseous (NO(x), CO, SO(2)) and aerosol (black carbon, organic matter, sulfate) species for different kinds of low-sulfur fuels in shipping. We apply these inventories to study the resulting changes in radiative forcing, attributed to particles from shipping, with the global aerosol-climate model EMAC-MADE. The emission factors for the different fuels are based on measurements at a test bed of a large diesel engine. We consider both fossil fuel (marine gas oil) and biofuels (palm and soy bean oil) as a substitute for heavy fuel oil in the current (2006) fleet and compare their climate impact to that resulting from heavy fuel oil use. Our simulations suggest that ship-induced surface level concentrations of sulfate aerosol are strongly reduced, up to about 40-60% in the high-traffic regions. This clearly has positive consequences for pollution reduction in the vicinity of major harbors. Additionally, such reductions in the aerosol loading lead to a decrease of a factor of 3-4 in the indirect global aerosol effect induced by emissions from international shipping.

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

    NASA Technical Reports Server (NTRS)

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

    2012-01-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2015-04-01

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

  17. Influence of local and regional sources on the observed spatial and temporal variability of size resolved atmospheric aerosol mass concentrations and water-soluble species in the Athens metropolitan area

    NASA Astrophysics Data System (ADS)

    Eleftheriadis, Konstantinos; Ochsenkuhn, Klaus M.; Lymperopoulou, Theopisti; Karanasiou, Angeliki; Razos, Panayiotis; Ochsenkuhn-Petropoulou, Maria

    2014-11-01

    The variability of common aerosol species in large Metropolitan urban areas is a major air quality issue with strong health impacts of large populations. PM10 and PM2.5 particulate matter samples were obtained at three sites characteristic of industrial, urban traffic and sub-urban residential areas in the Athens basin. Samples were analysed for anions (Cl-, NO3-, SO42-) and cations (K+, Na+, Ca2+, Mg2+, NH4+) using ion chromatography. The spatial and temporal variability for the particulate matter (PM) concentration mass and water-soluble ionic species concentrations for the investigated sites were studied. Mean PM fine concentration levels were 20% higher at the industrial and the central urban areas compared to those in the suburban area (24.2 μg/m3). The mean values for the coarse fraction at those two sites were two to three times higher compared to those at the suburban site (12.4 μg/m3). Comparable concentration levels of most species were observed in all areas, while SO42- and NO3- differ at a significant level. Furthermore, the average size distributions of the mass and individual ions at the suburban site (NCSR Demokritos) showed a bimodal size distribution. SO42- and NH4+ have their main peak in the fine fraction while NO3- showed equal distribution on the fine and coarse mode.. Good correlation was found for SO42- and NO3- with Ca2+ and Na+ with Cl- for the coarse fraction in the industrial area. NH4+ was closely correlated with SO42- in the fine particles and in all areas. For the urban site the best correlations in coarse particulates were reported between Na+/Mg2+-Cl-, Ca2+/Mg2+-SO42-, explained by neutralization of acidic aerosol by soil dust and sea salt in the coarse fraction. Moreover, time weighted concentrations roses at the industrial and urban sites, showed no significant directional dependence, indicating either uniform generation of mainly the coarse species within the metropolitan area or major influence of the regional background for

  18. Aerosol Blanket Likely Thinned During 1990s

    NASA Technical Reports Server (NTRS)

    2007-01-01

    Each day, a blanket of tiny particles drifting through the Earth's atmosphere filters out some of the sunlight headed for the planet's surface. These aerosols, including dust, smoke, and human-produced pollution, can reflect incoming light or absorb it, directly affecting the Earth's energy balance and climate. Aerosols also influence the climate indirectly, by affecting the brightness and amount of clouds. Research by NASA scientists on global aerosol patterns since the 1990s indicate the global aerosol blanket has likely thinned, allowing more sunlight to reach the Earth's surface over the past decade. The thinning of the blanket is shown by this trio of images based on satellite observations of aerosol optical thickness, a measurement that scientists use to describe how much the aerosols filter the incoming sunlight. Higher optical thickness (orange and red) means more sunlight blocking. The globes show average aerosol optical thickness for 1988-1991 (top), 2002-2005 (middle), and the change between the two time periods (bottom). Overall, the 1988-1991 image appears redder, a sign that aerosols were blocking more incoming sunlight; the 2002-2005 image has more light yellow areas. In the bottom image, small pockets of red (increased aerosol optical thickness), mostly near land masses in the Northern Hemisphere, are far outnumbered by blue areas (decreased aerosol optical thickness). Because they block incoming sunlight from reaching Earth's surface, aerosols may counterbalance greenhouse gas warming. The decline in the dimming power of aerosols over the past decade may have made the greenhouse warming trend more evident in the past decade than in previous decades. The scientists describe their results as a 'likely' trend because the National Oceanic and Atmospheric Administration satellite sensors they used in their analysis were not specifically designed to observe aerosols, and may contain some errors. However, specific, major aerosol events, such as large

  19. Unidirectional perfect absorber

    PubMed Central

    Jin, L.; Wang, P.; Song, Z.

    2016-01-01

    This study proposes a unidirectional perfect absorber (UPA), which we realized with a two-arm Aharonov-Bohm interferometer, that consists of a dissipative resonator side-coupled to a uniform resonator array. The UPA has reflection-less full absorption on one direction, and reflectionless full transmission on the other, with an appropriate magnetic flux and coupling, detuning, and loss of the side-coupled resonator. The magnetic flux controls the transmission, the left transmission is larger for magnetic flux less than one-half flux quantum; and the right transmission is larger for magnetic flux between one-half and one flux quantum. Besides, a perfect absorber (PA) can be realized based on the UPA, in which light waves from both sides, with arbitrary superposition of the ampli- tude and phase, are perfectly absorbed. The UPA is expected to be useful in the design of novel optical devices. PMID:27615125

  20. Shock absorber servicing tool

    NASA Technical Reports Server (NTRS)

    Koepler, Jack L. (Inventor); Hill, Robert L. (Inventor)

    1981-01-01

    A tool to assist in the servicing of a shock absorber wherein the shock absorber is constructed of a pair of aligned gas and liquid filled chambers. Each of the chambers is separated by a movable separator member. Maximum efficiency of the shock absorber is achieved in the locating of a precise volume of gas within the gas chamber and a precise volume of liquid within the liquid chamber. The servicing tool of this invention employs a rod which is to connect with the separator and by observation of the position of the rod with respect to the gauge body, the location of the separator is ascertained even though it is not directly observable.

  1. Unidirectional perfect absorber

    NASA Astrophysics Data System (ADS)

    Jin, L.; Wang, P.; Song, Z.

    2016-09-01

    This study proposes a unidirectional perfect absorber (UPA), which we realized with a two-arm Aharonov-Bohm interferometer, that consists of a dissipative resonator side-coupled to a uniform resonator array. The UPA has reflection-less full absorption on one direction, and reflectionless full transmission on the other, with an appropriate magnetic flux and coupling, detuning, and loss of the side-coupled resonator. The magnetic flux controls the transmission, the left transmission is larger for magnetic flux less than one-half flux quantum; and the right transmission is larger for magnetic flux between one-half and one flux quantum. Besides, a perfect absorber (PA) can be realized based on the UPA, in which light waves from both sides, with arbitrary superposition of the ampli- tude and phase, are perfectly absorbed. The UPA is expected to be useful in the design of novel optical devices.

  2. Shock Absorbing System

    NASA Astrophysics Data System (ADS)

    1982-01-01

    A lightweight, inexpensive shock-absorbing system, developed by Langley Research Center 20 years ago, is now in service as safety device for an automated railway at Duke University Medical Center. The transportation system travels at about 25 miles per hour, carrying patients, visitors, staff and cargo. At the end of each guideway of the system are "frangible," (breakable) tube "buffers." If a slowing car fails to make a complete stop at the terminal, it would bump and shatter the tubes, absorbing energy that might otherwise jolt the passengers or damage the vehicle.

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

    NASA Astrophysics Data System (ADS)

    Yoon, Jongmin; Kokhanovsky, Alexander

    2015-04-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2007-12-01

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

  5. Inferring Absorbing Organic Carbon Content from AERONET Data

    NASA Technical Reports Server (NTRS)

    Arola, A.; Schuster, G.; Myhre, G.; Kazadzis, S.; Dey, S.; Tripathi, S. N.

    2011-01-01

    Black carbon, light-absorbing organic carbon (often called brown carbon) and mineral dust are the major light-absorbing aerosols. Currently the sources and formation of brown carbon aerosol in particular are not well understood. In this study we estimated globally the amount of light absorbing organic carbon and black carbon from AERONET measurements. We find that the columnar absorbing organic carbon (brown carbon) levels in biomass burning regions of South-America and Africa are relatively high (about 15-20 magnesium per square meters during biomass burning season), while the concentrations are significantly lower in urban areas in US and Europe. However, we estimated significant absorbing organic carbon amounts from the data of megacities of newly industrialized countries, particularly in India and China, showing also clear seasonality with peak values up to 30-35 magnesium per square meters during the coldest season, likely caused by the coal and biofuel burning used for heating. We also compared our retrievals with the modeled organic carbon by global Oslo CTM for several sites. Model values are higher in biomass burning regions than AERONET-based retrievals, while opposite is true in urban areas in India and China.

  6. Assessment of aerosol-cloud interactions during southern African biomass burning activity, employing cloud parameterizations

    NASA Astrophysics Data System (ADS)

    Wiston, Modise; McFiggans, Gordon; Schultz, David

    2015-04-01

    In this study, we perform a simulation of the spatial distributions of particle and gas concentrations from a significantly large source of pollution event during a dry season in southern Africa and their interactions with cloud processes. Specific focus is on the extent to which cloud-aerosol interactions are affected by various inputs (i.e. emissions) and parameterizations and feedback mechanisms in a coupled mesoscale chemistry-meteorology model -herein Weather Research and Forecasting model with chemistry (WRF-Chem). The southern African dry season (May-Sep) is characterised by biomass burning (BB) type of pollution. During this period, BB particles are frequently observed over the subcontinent, at the same time a persistent deck of stratocumulus covers the south West African coast, favouring long-range transport over the Atlantic Ocean of aerosols above clouds. While anthropogenic pollutants tend to spread more over the entire domain, biomass pollutants are concentrated around the burning areas, especially the savannah and tropical rainforest of the Congo Basin. BB is linked to agricultural practice at latitudes south of 10° N. During an intense burning event, there is a clear signal of strong interactions of aerosols and cloud microphysics. These species interfere with the radiative budget, and directly affect the amount of solar radiation reflected and scattered back to space and partly absorbed by the atmosphere. Aerosols also affect cloud microphysics by acting as cloud condensation nuclei (CCN), modifying precipitation pattern and the cloud albedo. Key area is to understand the role of pollution on convective cloud processes and its impacts on cloud dynamics. The hypothesis is that an environment of potentially high pollution enables the probability of interactions between co-located aerosols and cloud layers. To investigate this hypothesis, we outline an approach to integrate three elements: i) focusing on regime(s) where there are strong indications of

  7. Organic matrix effects on the formation of light-absorbing compounds from α-dicarbonyls in aqueous salt solution.

    PubMed

    Drozd, Greg T; McNeill, V Faye

    2014-04-01

    Aqueous-phase reactions of organic compounds are of general importance in environmental systems. Reactions of α-dicarbonyl compounds in the aqueous phase of atmospheric aerosols can impact their climate-relevant physical properties including hygroscopicity and absorption of light. Less-reactive water-soluble organic compounds may contribute an organic matrix component to the aqueous environment, potentially impacting the reaction kinetics. In this work we demonstrate the effects of organic matrices on the self-reactions of glyoxal (Gly) and methylglyoxal (mGly) in aqueous solutions containing ammonium sulfate. At an organic-to-sulfate mass ratio of 2 : 1, carbohydrate-like matrices resembling oxidized organic aerosol material reduce the rate of formation of light-absorbing products by up to an order of magnitude. The greatest decreases in the reaction rates were observed for organic matrices with smaller, more linear molecular structures. Initial UV-Vis spectra, product studies, relative rate data, acidity changes, and viscosity measurements suggest that shifts in carbonyl equilibria, due in part to (hemi)acetal formation with the matrix, reduce the rate of formation of light-absorbing imidazole and oligomer species.

  8. ENCAPSULATED AEROSOLS

    DTIC Science & Technology

    materials determine the range of applicability of each method. A useful microencapsulation method, based on coagulation by inertial force was developed...The generation apparatus, consisting of two aerosol generators in series, was utilized to produce many kinds of microcapsules . A fluid energy mill...was found useful for the production of some microcapsules . The permeability of microcapsule films and the effect of exposure time and humidity were

  9. Solar concentrator/absorber

    NASA Technical Reports Server (NTRS)

    Von Tiesenhausen, G. F.

    1976-01-01

    Collector/energy converter, consisting of dual-slope optical concentrator and counterflow thermal energy absorber, is attached to multiaxis support structure. Efficient over wide range of illumination levels, device may be used to generate high temperature steam, serve as solar powered dryer, or power absorption cycle cooler.

  10. Neutron Absorbing Alloys

    SciTech Connect

    Mizia, Ronald E.; Shaber, Eric L.; DuPont, John N.; Robino, Charles V.; Williams, David B.

    2004-05-04

    The present invention is drawn to new classes of advanced neutron absorbing structural materials for use in spent nuclear fuel applications requiring structural strength, weldability, and long term corrosion resistance. Particularly, an austenitic stainless steel alloy containing gadolinium and less than 5% of a ferrite content is disclosed. Additionally, a nickel-based alloy containing gadolinium and greater than 50% nickel is also disclosed.

  11. Shock Absorbing Helmets

    NASA Technical Reports Server (NTRS)

    1978-01-01

    This paper presents a description of helmets used by football players that offer three times the shock-absorbing capacity of earlier types. An interior padding for the helmets, composed of Temper Foam, first used by NASA's Ames Research Center in the design of aircraft seats is described.

  12. Aerosol Climate Time Series in ESA Aerosol_cci

    NASA Astrophysics Data System (ADS)

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

    2016-04-01

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

  13. Does the Madden-Julian Oscillation Influence Aerosol Variability?

    NASA Astrophysics Data System (ADS)

    Tian, B.; Waliser, D. E.; Kahn, R. A.; Li, Q.; Yung, Y. L.; Tyranowski, T.; Geogdzhayev, I. V.; Mishchenko, M. I.; Torres, O.; Smirnov, A.

    2007-12-01

    We investigate the modulation of aerosols by the Madden-Julian Oscillation (MJO) using satellite-based global aerosol products, including aerosol index (AI) from the Total Ozone Mapping Spectrometer (TOMS) on Nimbus-7, and aerosol optical thickness (AOT) from the Moderate Resolution Imaging Spectroradiometer (MODIS) on Terra and Aqua and the Advanced Very High Resolution Radiometer (AVHRR) on NOAA satellites. A composite analysis is performed for boreal winter, and the global pentad rainfall data from the NOAA Climate Prediction Center (CPC) Merged Analysis of Precipitation (CMAP) are used to identify MJO events. The MJO composites exhibit large variations in the TOMS AI and MODIS/AVHRR AOT over the equatorial Indian and western Pacific Oceans where MJO convection is active, as well as the tropical Africa and Atlantic Ocean where MJO convection is relatively weak but the background aerosol level is relatively high. A strong inverse linear relationship between the TOMS AI and rainfall anomalies, but a weaker, less coherent positive correlation between the MODIS/AVHRR AOT and rainfall anomalies, were found. The Aerosol Robotic Network AOT pattern at Kaashidoo (73.5°E, 4.9°N) and Nauru (167°E, 0.5°S) is more consistent with MODIS and AVHRR. These results indicate a connection between the MJO, its associated rainfall and circulation variability, and the observed aerosol variations. Several physical and non-physical factors that may contribute to the observed aerosol-rainfall relationship, such as aerosol humidification effect, wet deposition, surface wind speed, phytoplankton, different sensor sensitivities (absorbing versus non-absorbing aerosols and upper versus lower tropospheric aerosols), sampling issue, and cloud contamination, are discussed. However, a clear causal explanation for the observed patterns remains elusive. Further investigation is needed to unravel this complex aerosol-rainfall relationship.

  14. Retrieval of Aerosol Absorption Properties from Satellite Observations

    NASA Technical Reports Server (NTRS)

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

    2012-01-01

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

  15. Photothermal spectroscopy of aerosols

    SciTech Connect

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

    1981-04-01

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

  16. Influence of crustal dust and sea spray supermicron particle concentrations and acidity on inorganic NO3− aerosol during the 2013 Southern Oxidant and Aerosol Study

    DOE PAGES

    Allen, H. M.; Draper, D. C.; Ayres, B. R.; ...

    2015-09-25

    Inorganic aerosol composition was measured in the southeastern United States, a region that exhibits high aerosol mass loading during the summer, as part of the 2013 Southern Oxidant and Aerosol Study (SOAS) campaign. Measurements using a Monitor for AeRosols and GAses (MARGA) revealed two periods of high aerosol nitrate (NO3−) concentrations during the campaign. These periods of high nitrate were correlated with increased concentrations of supermicron crustal and sea spray aerosol species, particularly Na+ and Ca2+, and with a shift towards aerosol with larger (1 to 2.5 μm) diameters. We suggest this nitrate aerosol forms by multiphase reactions of HNO3more » and particles, reactions that are facilitated by transport of crustal dust and sea spray aerosol from a source within the United States. The observed high aerosol acidity prevents the formation of NH4NO3, the inorganic nitrogen species often dominant in fine-mode aerosol at higher pH. In addition, calculation of the rate of the heterogeneous uptake of HNO3 on mineral aerosol supports the conclusion that aerosol NO3− is produced primarily by this process, and is likely limited by the availability of mineral cation-containing aerosol surface area. Modeling of NO3− and HNO3 by thermodynamic equilibrium models (ISORROPIA II and E-AIM) reveals the importance of including mineral cations in the southeastern United States to accurately balance ion species and predict gas–aerosol phase partitioning.« less

  17. Implementation of the Missing Aerosol Physics into LLNL IMPACT

    SciTech Connect

    Chuang, C

    2005-02-09

    In recent assessments of climate forcing, the Intergovernmental Panel on Climate Change lists aerosol as one o f the most important anthropogenic agents that influence climate. Atmospheric aerosols directly affect the radiative fluxes at the surface and top of the Earth's atmosphere by scattering and/or absorbing radiation. Further, aerosols indirectly change cloud microphysical properties (such as cloud drop effective radius) that also affect the radiative fluxes. However, the estimate of the magnitude of aerosol climatic effect varies widely, and aerosol/cloud interactions remain one of the most uncertain aspects of climate models today. The Atmospheric Sciences Division has formulated a plan to enhance and expand our modeling expertise in aerosol/cloud/climate interactions. Under previous LDRD support, we successfully developed a computationally efficient version of IMPACT to simulate aerosol climatology. This new version contains a compact chemical mechanism for the prediction of sulfate and also predicts the distributions of organic carbon (OC), black carbon (BC), dust, and sea salt. Furthermore, we implemented a radiation package into IMPACT to calculate the radiative forcing and heating/cooling rates by aerosols. This accomplishment built the foundation of our currently funded projects under the NASA Global Modeling and Analysis Program as well as the DOE Atmospheric Radiation Program. Despite the fact that our research is being recognized as an important effort to quantify the effects of anthropogenic aerosols on climate, the major shortcoming of our previous simulations on aerosol climatic effects is the over simplification of spatial and temporal variations of aerosol size distributions that are shaped by complicated nucleation, growth, transport and removal processes. Virtually all properties of atmospheric aerosols and clouds depend strongly on aerosol size distribution. Moreover, molecular processing on aerosol surfaces alters the hygroscopic

  18. Measurements of Acidic Gases and Aerosol Species Aboard the NASA DC-8 Aircraft During the Pacific Exploratory Mission in the Tropics (PEM-Tropics A)

    NASA Technical Reports Server (NTRS)

    Talbot, Robert W.; Dibb, Jack E.

    1999-01-01

    We received funding to provide measurements of nitric acid (HNO3), formic acid (HCOOH), acetic acid (CH3COOH), and the chemical composition of aerosols aboard the NASA Ames DC-8 research aircraft during the PEM-Tropics A mission. These measurements were successfully completed and the final data resides in the electronic archive (ftp-gte.larc.nasa.gov) at NASA Langley Research Center. For the PEM-Tropics A mission the University of New Hampshire group was first author of four different manuscripts. Three of these have now appeared in the Journal of Geophysical Research-Atmospheres, included in the two section sections on PEM-Tropics A. The fourth manuscript has just recently been submitted to this same journal as a stand alone paper. All four of these papers are included in this report. The first paper (Influence of biomass combustion emissions on the distribution of acidic trace gases over the Southern Pacific basin during austral springtime) describes the large-scale distributions of HNO3, HCOOH, and CH3COOH. Arguments were presented to show, particularly in the middle tropospheric region, that biomass burning emissions from South America and Africa were a major source of acidic gases over the South Pacific basin. The second paper (Aerosol chemical composition and distribution during the Pacific Exploratory Mission (PEM) Tropics) covers the aerosol aspects of our measurement package. Compared to acidic gases, O3, and selected hydrocarbons, the aerosol chemistry showed little influence from biomass burning emissions. The data collected in the marine boundary layer showed a possible marine source of NH3 to the troposphere in equatorial areas. This source had been speculated on previously, but our data was the first collected from an airborne platform to show its large-scale features. The third paper (Constraints on the age and dilution of Pacific Exploratory Mission-Tropics biomass burning plumes from the natural radionuclide tracer Pb-210) utilized the unexpectedly

  19. Global measurements of gaseous and aerosol trace species in the upper troposphere and lower stratosphere from daily flights of 747 airliners

    NASA Technical Reports Server (NTRS)

    Perkins, P. J.

    1976-01-01

    Extensive measurements include ozone, carbon monoxide, water vapor, and aerosol and condensation nuclei number density. Less extensive measurements include chlorofluoromethanes, sulfates and nitrates. Certain meteorological and flight information are also recorded at the time of these measurements. World routes range in latitude from about 60 deg N near North America to about 40 deg S over Australia and 23 deg S over South America. Typical data show significant changes in ozone, carbon monoxide, and water vapor when crossing the tropopause either during changes in altitude or at cruise altitude. These gases as well as light scattering particles and condensation nuclei exhibit considerable variability along a flight route.

  20. Simulations of the Aerosol Index and the Absorption Aerosol Optical Depth and Comparisons with OMI Retrievals During ARCTAS-2008 Campaign

    NASA Technical Reports Server (NTRS)

    2010-01-01

    We have computed the Aerosol Index (AI) at 354 nm, useful for observing the presence of absorbing aerosols in the atmosphere, from aerosol simulations conducted with the Goddard Chemistry, Aerosol, Radiation, and Transport (GOCART) module running online the GEOS-5 Atmospheric GCM. The model simulates five aerosol types: dust, sea salt, black carbon, organic carbon and sulfate aerosol and can be run in replay or data assimilation modes. In the assimilation mode, information's provided by the space-based MODIS and MISR sensors constrains the model aerosol state. Aerosol optical properties are then derived from the simulated mass concentration and the Al is determined at the OMI footprint using the radiative transfer code VLIDORT. In parallel, model derived Absorption Aerosol Optical Depth (AAOD) is compared with OMI retrievals. We have focused our study during ARCTAS (June - July 2008), a period with a good sampling of dust and biomass burning events. Our ultimate goal is to use OMI measurements as independent validation for our MODIS/MISR assimilation. Towards this goal we document the limitation of OMI aerosol absorption measurements on a global scale, in particular sensitivity to aerosol vertical profile and cloud contamination effects, deriving the appropriate averaging kernels. More specifically, model simulated (full) column integrated AAOD is compared with model derived Al, this way identifying those regions and conditions under which OMI cannot detect absorbing aerosols. Making use of ATrain cloud measurements from MODIS, C1oudSat and CALIPSO we also investigate the global impact on clouds on OMI derived Al, and the extent to which GEOS-5 clouds can offer a first order representation of these effects.

  1. Longwave radiative forcing by aqueous aerosols

    SciTech Connect

    Gaffney, J.S.; Marley, N.A.

    1995-01-01

    Recently, a great deal of interest has been focused on the role of aerosols in climatic change because of their potential cooling impacts due to light scattering. Recent advances in infrared spectroscopy using cylindrical internal reflectance have allowed the longwave absorption of dissolved aerosol species and the associated liquid water to be accurately determined and evaluated. Experimental measurements using these techniques have shown that dissolved sulfate, nitrate, and numerous other aerosol species will act to cause greenhouse effects. Preliminary calculations indicate that the longwave climate forcing (i.e., heating) for sulfate aerosol will be comparable in magnitude to the cooling effect produced by light scattering. However, more detailed modeling will clearly be needed to address the impact of the longwave forcing due to aerosols as a function of atmospheric height and composition. Their work has shown that aerosol composition will be important in determining longwave forcing, while shortwave forcing will be more related to the physical size of the aerosol droplets. On the basis of these studies, it is increasingly apparent that aerosols, fogs, and clouds play a key role in determining the radiative balance of the atmosphere and in controlling regional and global climates.

  2. How We Can Constrain Aerosol Type Globally

    NASA Technical Reports Server (NTRS)

    Kahn, Ralph

    2016-01-01

    species-specific aerosol mass and size that are tracked in aerosol transport and climate models used to assess aerosol forcing and its anthropogenic components. This presentation will summarize where we stand on the development of the SAM-CAAM concept.

  3. Identification of oxidized organic atmospheric species during the Southern Oxidant and Aerosol Study (SOAS) using a novel Ion Mobility Time-of-Flight Chemical Ionization Mass Spectrometer (IMS-ToF-CIMS)

    NASA Astrophysics Data System (ADS)

    Krechmer, J.; Canagaratna, M.; Kimmel, J.; Junninen, H.; Knochenmuss, R.; Cubison, M.; Massoli, P.; Stark, H.; Jayne, J. T.; Surratt, J. D.; Jimenez, J. L.; Worsnop, D. R.

    2013-12-01

    We present results from the field deployment of a novel Ion Mobility Time-of-flight Chemical Ionization Mass Spectrometer (CI-IMS-TOF) during the Southern Oxidant and Aerosol Study (SOAS). IMS-TOF is a 2-dimensional analysis method, which separates gas-phase ions by mobility prior to determination of mass-to-charge ratio by mass spectrometry. Ion mobility is a unique physical property that is determined by the collisional cross section of an ion. Because mobility depends on size and shape, the IMS measurement is able to resolve isomers and isobaric compounds. Additionally, trends in IMS-TOF data space can be used to identify relationships between ions, such as common functionality or polymeric series. During SOAS we interfaced the IMS-TOF to a nitrate ion (NO3-) chemical ionization source that enables the selective ionization of highly oxidized gas phase species (those having a high O:C ratio) through clustering with the reagent ion. Highly oxidized products of terpenes and isoprene are important secondary organic aerosol precursors (SOA) that play an uncertain but important role in particle-phase chemistry. We present several case studies of atmospheric events during SOAS that exhibited elevated concentrations of sulfuric acid and/or organics. These events exhibited a rise in particle number and provide an opportunity to examine the role that organic species may have in local atmospheric new particle formation events. We also present the results from the field deployment and subsequent laboratory studies utilizing a Potential Aerosol Mass (PAM) flow reactor as the inlet for the CI-IMS-TOF. The reactor draws in ambient air and exposes it to high concentrations of the OH radical, created by photolysis O3 in the presence of water. The highly oxidized products are then sampled directly by the CI-IMS-TOF. We performed several experiments including placing pine and deciduous plants directly in front of the reactor opening and observed large increases in the number and

  4. Retrieval of Aerosol Optical Depth Above Clouds from OMI Observations: Sensitivity Analysis, Case Studies

    NASA Technical Reports Server (NTRS)

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

    2012-01-01

    A large fraction of the atmospheric aerosol load reaching the free troposphere is frequently located above low clouds. Most commonly observed aerosols above clouds are carbonaceous particles generally associated with biomass burning and boreal forest fires, and mineral aerosols originated in arid and semi-arid regions and transported across large distances, often above clouds. Because these aerosols absorb solar radiation, their role in the radiative transfer balance of the earth atmosphere system is especially important. The generally negative (cooling) top of the atmosphere direct effect of absorbing aerosols, may turn into warming when the light-absorbing particles are located above clouds. The actual effect depends on the aerosol load and the single scattering albedo, and on the geometric cloud fraction. In spite of its potential significance, the role of aerosols above clouds is not adequately accounted for in the assessment of aerosol radiative forcing effects due to the lack of measurements. In this paper we discuss the basis of a simple technique that uses near-UV observations to simultaneously derive the optical depth of both the aerosol layer and the underlying cloud for overcast conditions. The two-parameter retrieval method described here makes use of the UV aerosol index and reflectance measurements at 388 nm. A detailed sensitivity analysis indicates that the measured radiances depend mainly on the aerosol absorption exponent and aerosol-cloud separation. The technique was applied to above-cloud aerosol events over the Southern Atlantic Ocean yielding realistic results as indicated by indirect evaluation methods. An error analysis indicates that for typical overcast cloudy conditions and aerosol loads, the aerosol optical depth can be retrieved with an accuracy of approximately 54% whereas the cloud optical depth can be derived within 17% of the true value.

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

    NASA Astrophysics Data System (ADS)

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

    2016-04-01

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

  6. Impact of the modal aerosol scheme GLOMAP-mode on aerosol forcing in the Hadley Centre Global Environmental Model

    NASA Astrophysics Data System (ADS)

    Bellouin, N.; Mann, G. W.; Woodhouse, M. T.; Johnson, C.; Carslaw, K. S.; Dalvi, M.

    2013-03-01

    The Hadley Centre Global Environmental Model (HadGEM) includes two aerosol schemes: the Coupled Large-scale Aerosol Simulator for Studies in Climate (CLASSIC), and the new Global Model of Aerosol Processes (GLOMAP-mode). GLOMAP-mode is a modal aerosol microphysics scheme that simulates not only aerosol mass but also aerosol number, represents internally-mixed particles, and includes aerosol microphysical processes such as nucleation. In this study, both schemes provide hindcast simulations of natural and anthropogenic aerosol species for the period 2000-2006. HadGEM simulations of the aerosol optical depth using GLOMAP-mode compare better than CLASSIC against a data-assimilated aerosol re-analysis and aerosol ground-based observations. Because of differences in wet deposition rates, GLOMAP-mode sulphate aerosol residence time is two days longer than CLASSIC sulphate aerosols, whereas black carbon residence time is much shorter. As a result, CLASSIC underestimates aerosol optical depths in continental regions of the Northern Hemisphere and likely overestimates absorption in remote regions. Aerosol direct and first indirect radiative forcings are computed from simulations of aerosols with emissions for the year 1850 and 2000. In 1850, GLOMAP-mode predicts lower aerosol optical depths and higher cloud droplet number concentrations than CLASSIC. Consequently, simulated clouds are much less susceptible to natural and anthropogenic aerosol changes when the microphysical scheme is used. In particular, the response of cloud condensation nuclei to an increase in dimethyl sulphide emissions becomes a factor of four smaller. The combined effect of different 1850 baselines, residence times, and abilities to affect cloud droplet number, leads to substantial differences in the aerosol forcings simulated by the two schemes. GLOMAP-mode finds a present-day direct aerosol forcing of -0.49 W m-2 on a global average, 72% stronger than the corresponding forcing from CLASSIC. This

  7. Metasurface Broadband Solar Absorber

    PubMed Central

    Azad, Abul K.; Kort-Kamp, Wilton J. M.; Sykora, Milan; Weisse-Bernstein, Nina R.; Luk, Ting S.; Taylor, Antoinette J.; Dalvit, Diego A. R.; Chen, Hou-Tong

    2016-01-01

    We demonstrate a broadband, polarization independent, wide-angle absorber based on a metallic metasurface architecture, which accomplishes greater than 90% absorptance in the visible and near-infrared range of the solar spectrum, and exhibits low absorptivity (emissivity) at mid- and far-infrared wavelengths. The complex unit cell of the metasurface solar absorber consists of eight pairs of gold nano-resonators that are separated from a gold ground plane by a thin silicon dioxide spacer. Our experimental measurements reveal high-performance absorption over a wide range of incidence angles for both s- and p-polarizations. We also investigate numerically the frequency-dependent field and current distributions to elucidate how the absorption occurs within the metasurface structure. PMID:26828999

  8. Metasurface Broadband Solar Absorber

    DOE PAGES

    Azad, Abul K.; Kort-Kamp, Wilton J. M.; Sykora, Milan; ...

    2016-02-01

    Here, we demonstrate a broadband, polarization independent, wide-angle absorber based on a metallic metasurface architecture, which accomplishes greater than 90% absorptance in the visible and near-infrared range of the solar spectrum, and exhibits low absorptivity (emissivity) at mid- and far-infrared wavelengths. The complex unit cell of the metasurface solar absorber consists of eight pairs of gold nano-resonators that are separated from a gold ground plane by a thin silicon dioxide spacer. Moreover, our experimental measurements reveal high-performance absorption over a wide range of incidence angles for both s- and p-polarizations. We also investigate numerically the frequency-dependent field and current distributionsmore » to elucidate how the absorption occurs within the metasurface structure.« less

  9. Metasurface Broadband Solar Absorber

    SciTech Connect

    Azad, Abul K.; Kort-Kamp, Wilton J. M.; Sykora, Milan; Weisse-Bernstein, Nina R.; Luk, Ting S.; Taylor, Antoinette J.; Dalvit, Diego A. R.; Chen, Hou-Tong

    2016-02-01

    Here, we demonstrate a broadband, polarization independent, wide-angle absorber based on a metallic metasurface architecture, which accomplishes greater than 90% absorptance in the visible and near-infrared range of the solar spectrum, and exhibits low absorptivity (emissivity) at mid- and far-infrared wavelengths. The complex unit cell of the metasurface solar absorber consists of eight pairs of gold nano-resonators that are separated from a gold ground plane by a thin silicon dioxide spacer. Moreover, our experimental measurements reveal high-performance absorption over a wide range of incidence angles for both s- and p-polarizations. We also investigate numerically the frequency-dependent field and current distributions to elucidate how the absorption occurs within the metasurface structure.

  10. Oxalate: Effect on calcium absorbability

    SciTech Connect

    Heaney, R.P.; Weaver, C.M. )

    1989-10-01

    Absorption of calcium from intrinsically labeled Ca oxalate was measured in 18 normal women and compared with absorption of Ca from milk in these same subjects, both when the test substances were ingested in separate meals and when ingested together. Fractional Ca absorption from oxalate averaged 0.100 +/- 0.043 when ingested alone and 0.140 +/- 0.063 when ingested together with milk. Absorption was, as expected, substantially lower than absorption from milk (0.358 +/- 0.113). Nevertheless Ca oxalate absorbability in these women was higher than we had previously found for spinach Ca. When milk and Ca oxalate were ingested together, there was no interference of oxalate in milk Ca absorption and no evidence of tracer exchange between the two labeled Ca species.

  11. Lidar remote sensing of laser-induced incandescence on light absorbing particles in the atmosphere.

    PubMed

    Miffre, Alain; Anselmo, Christophe; Geffroy, Sylvain; Fréjafon, Emeric; Rairoux, Patrick

    2015-02-09

    Carbon aerosol is now recognized as a major uncertainty on climate change and public health, and specific instruments are required to address the time and space evolution of this aerosol, which efficiently absorbs light. In this paper, we report an experiment, based on coupling lidar remote sensing with Laser-Induced-Incandescence (LII), which allows, in agreement with Planck's law, to retrieve the vertical profile of very low thermal radiation emitted by light-absorbing particles in an urban atmosphere over several hundred meters altitude. Accordingly, we set the LII-lidar formalism and equation and addressed the main features of LII-lidar in the atmosphere by numerically simulating the LII-lidar signal. We believe atmospheric LII-lidar to be a promising tool for radiative transfer, especially when combined with elastic backscattering lidar, as it may then allow a remote partitioning between strong/less light absorbing carbon aerosols.

  12. Ionized Absorbers in AGN

    NASA Technical Reports Server (NTRS)

    Mathur, S.

    1999-01-01

    As a part of this program, we observed three AGN:PKS2251 + 113, PG0043 = 039 and PLH909. Two objects show signatures of absorbtion in their UV spectra. Based on our earlier modeling of X-ray warm absorbents, we expected to observe X-ray observation in these objects. The third, PLH909, is known to have soft excess in EINSTEIN data. Attachment: "Exploratory ASCA observation of broad absorption line quasi-stellar objects".

  13. Apollo couch energy absorbers

    NASA Technical Reports Server (NTRS)

    Wesselski, C. J.; Drexel, R. E.

    1972-01-01

    Load attenuators for the Apollo spacecraft crew couch and its potential applications are described. Energy absorption is achieved through friction and cyclic deformation of material. In one concept, energy absorption is accomplished by rolling a compressed ring of metal between two surfaces. In another concept, energy is absorbed by forcing a plastically deformed washer along a rod. Among the design problems that had to be solved were material selection, fatigue life, ring slippage, lubrication, and friction loading.

  14. In-Situ Measurements of Aerosol Optical Properties using New Cavity Ring-Down and Photoacoustics Instruments and Comparison with more Traditional Techniques

    NASA Technical Reports Server (NTRS)

    Strawa, A. W.; Arnott, P.; Covert, D.; Elleman, R.; Ferrare, R.; Hallar, A. G.; Jonsson, H.; Kirchstetter, T. W.; Luu, A. P.; Ogren, J.

    2004-01-01

    Carbonaceous species (BC and OC) are responsible for most of the absorption associated with aerosol particles. The amount of radiant energy an aerosol absorbs has profound effects on climate and air quality. It is ironic that aerosol absorption coefficient is one of the most difficult aerosol properties to measure. A new cavity ring-down (CRD) instrument, called Cadenza (NASA-ARC), measures the aerosol extinction coefficient for 675 nm and 1550 nm light, and simultaneously measures the scattering coefficient at 675 nm. Absorption coefficient is obtained from the difference of measured extinction and scattering within the instrument. Aerosol absorption coefficient is also measured by a photoacoustic (PA) instrument (DRI) that was operated on an aircraft for the first time during the DOE Aerosol Intensive Operating Period (IOP). This paper will report on measurements made with this new instrument and other in-situ instruments during two field recent field studies. The first field study was an airborne cam;oaign, the DOE Aerosol Intensive Operating Period flown in May, 2003 over northern Oklahoma. One of the main purposes of the IOP was to assess our ability to measure extinction and absorption coefficient in situ. This paper compares measurements of these aerosol optical properties made by the CRD, PA, nephelometer, and Particle Soot Absorption Photometer (PSAP) aboard the CIRPAS Twin-Otter. During the IOP, several significant aerosol layers were sampled aloft. These layers are identified in the remote (AATS-14) as well as in situ measurements. Extinction profiles measured by Cadenza are compared to those derived from the Ames Airborne Tracking Sunphotometer (AATS-14, NASA-ARC). The regional radiative impact of these layers is assessed by using the measured aerosol optical properties in a radiative transfer model. The second study was conducted in the Caldecott Tunnel, a heavily-used tunnel located north of San Francisco, Ca. The aerosol sampled in this study was

  15. Subarctic atmospheric aerosol composition: 1. Ambient aerosol characterization

    SciTech Connect

    Friedman, Beth; Herich, Hanna; Kammermann, Lukas; Gross, Deborah S.; Ameth, Almut; Holst, Thomas; Lohmann, U.; Cziczo, Daniel J.

    2009-07-10

    Sub-Arctic aerosol was sampled during July 2007 at the Abisko Research Station Stordalen field site operated by the Royal Swedish Academy of Sciences. Located in northern Sweden at 68º latitude and 385 meters above sea level (msl), this site is classified as a semi-continuous permafrost mire. Number density, size distribution, cloud condensation nucleus properties, and chemical composition of the ambient aerosol were determined. Backtrajectories showed that three distinct airmasses were present over Stordalen during the sampling period. Aerosol properties changed and correlated with airmass origin to the south, northeast, or west. We observe that Arctic aerosol is not compositionally unlike that found in the free troposphere at mid-latitudes. Internal mixtures of sulfates and organics, many on insoluble biomass burning and/or elemental carbon cores, dominate the number density of particles from ~200 to 2000 nm aerodynamic diameter. Mineral dust which had taken up gas phase species was observed in all airmasses. Sea salt, and the extent to which it had lost volatile components, was the aerosol type that most varied with airmass.

  16. Investigation of aerosol optical properties for remote sensing through DRAGON (distributed regional aerosol gridded observation networks) campaign in Korea

    NASA Astrophysics Data System (ADS)

    Lim, Jae-Hyun; Ahn, Joon Young; Park, Jin-Soo; Hong, You-Deok; Han, Jin-Seok; Kim, Jhoon; Kim, Sang-Woo

    2014-11-01

    Aerosols in the atmosphere, including dust and pollutants, scatters/absorbs solar radiation and change the microphysics of clouds, thus influencing the Earth's energy budget, climate, air quality, visibility, agriculture and water circulation. Pollutants have also been reported to threaten the human health. The present research collaborated with the U.S. NASA and the U.S. Aerosol Robotic Network (AERONET) is to study the aerosol characteristics in East Asia and improve the long-distance transportation monitoring technology by analyzing the observations of aerosol characteristics in East Asia during Distributed Regional Aerosol Gridded Observation Networks (DRAGON) Campaign (March 2012-May 2012). The sun photometers that measure the aerosol optical characteristics were placed evenly throughout the Korean Peninsula and concentrated in Seoul and the metropolitan area. Observation data are obtained from the DRAGON campaign and the first year (2012) observation data (aerosol optical depth and aerosol spatial distribution) are analyzed. Sun photometer observations, including aerosol optical depth (AOD), are utilized to validate satellite observations from Geostationary Ocean Color Imager (GOCI) and Moderate Resolution Imaging Spectroradiometer (MODIS). Additional analysis is performed associated with the Northeast Asia, the Korean Peninsula in particular, to determine the spatial distribution of the aerosol.

  17. A review of atmospheric aerosol measurements

    NASA Astrophysics Data System (ADS)

    McMurry, Peter H.

    Recent developments in atmospheric aerosol measurements are reviewed. The topics included complement those covered in the recent review by Chow (JAWMA 45: 320-382, 1995) which focuses on regulatory compliance measurements and filter measurements of particulate composition. This review focuses on measurements of aerosol integral properties (total number concentration, CCN concentration, optical coefficients, etc.), aerosol physical chemical properties (density, refractive index, equilibrium water content, etc.), measurements of aerosol size distributions, and measurements of size-resolved aerosol composition. Such measurements play an essential role in studies of secondary aerosol formation by atmospheric chemical transformations and enable one to quantify the contributions of various species to effects including light scattering/absorption, health effects, dry deposition, etc. Aerosol measurement evolved from an art to a science in the 1970s following the development of instrumentation to generate monodisperse calibration aerosols of known size, composition, and concentration. While such calibration tools permit precise assessments of instrument responses to known laboratory-generated aerosols, unquantifiable uncertainties remain even when carefully calibrated instruments are used for atmospheric measurements. This is because instrument responses typically depend on aerosol properties including composition, shape, density, etc., which, for atmospheric aerosols, may vary from particle-to-particle and are often unknown. More effort needs to be made to quantify measurement accuracies that can be achieved for realistic atmospheric sampling scenarios. The measurement of organic species in atmospheric particles requires substantial development. Atmospheric aerosols typically include hundreds of organic compounds, and only a small fraction (˜10%) of these can be identified by state-of-the-art analytical methodologies. Even the measurement of the total particulate organic

  18. Aerosol volatility in a boreal forest environment

    NASA Astrophysics Data System (ADS)

    Häkkinen, S. A. K.; ńijälä, M.; Lehtipalo, K.; Junninen, H.; Virkkula, A.; Worsnop, D. R.; Kulmala, M.; Petäjä, T.; Riipinen, I.

    2012-04-01

    Climate and health effects of atmospheric aerosols are determined by their properties such as their chemical composition. Aerosol chemical composition can be studied indirectly by measuring volatility of aerosol particles. The volatility of submicron aerosol particles (20-500 nm) was studied in a boreal forest site at SMEAR II (Station for Measuring Ecosystem-Atmosphere Relations II) station (Vesala et al., 1998) in Hyytiälä, Finland, during 01/2008-05/2010. The instrument used for the measurements was VDMPS (Volatility Differential Mobility Particle Sizer), which consists of two separate instruments: DMPS (Differential Mobility Particle Sizer, Aalto et al., 2001) and TD (Thermodenuder, Wehner et al., 2002). Aerosol evaporation was examined by heating the aerosol and comparing the total aerosol mass before and after heating. In the VDMPS system ambient aerosol sample was heated up to temperatures ranging from 80 °C to 280 °C. The higher the heating temperature was the more aerosol material was evaporated. There was a non-volatile residual present in aerosol particles when heated up to 280 °C. This residual explained (20±8)% of the total aerosol mass. Aerosol non-volatile mass fraction was highest during winter and smallest during summer months. The role of black carbon in the observed non-volatile residual was determined. Black carbon explained 40 to 90% of the non-volatile mass. Especially during colder seasons noticeable amount of non-volatile material, something else than black carbon, was observed. According to Kalberer et al. (2004) some atmospheric organic species can form polymers that have high evaporation temperatures. Also low-volatile organic salts may contribute to the non-volatile aerosol (Smith et al., 2010). Aerosol mass composition measured directly with AMS (Aerosol Mass Spectrometer, Jayne et al., 2000) was analyzed in order to examine the properties of the non-volatile material (other than black carbon). The AMS measurements were performed

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

    NASA Technical Reports Server (NTRS)

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

    2001-01-01

    depth gradient, with AOD(500 nm) extremes from 0.1 to 1.1. On the Pacific transit from Honolulu to Hachijo AOD(500 nm) averaged 0.2, including increases to 0.4 after several storms, suggesting the strong impact of wind-generated seasalt. The AOD maximum, found in the Sea of Japan, was influenced by dust and anthropogenic sources. (4) In Beijing, single scattering albedo retrieved from AERONET sun-sky radiometry yielded midvisible SSA=0.88 with strong wavelength dependence, suggesting a significant black carbon component. SSA retrieved during dust episodes was approx. 0.90 and variable but wavelength neutral reflecting the presence of urban haze with the dust. Downwind at Anmyon Island SSA was considerably higher, approx. 0.94, but wavelength neutral for dust episodes and spectrally dependent during non dust periods. (5) Satellite retrievals show major aerosol features moving from Asia over the Pacific; however, determining seasonal-average aerosol effects is hampered by sampling frequency and large-scale cloud systems that obscure key parts of aerosol patterns. Preliminary calculations using, satellite-retrieved AOD fields and initial ACE-Asia aerosol properties (including sulfates, soot, and dust) yield clear-sky aerosol radiative effects in the seasonal-average ACE-Asia plume exceeding those of manmade greenhouse gases. Quantifying all-sky direct aerosol radiative effects is complicated by the need to define the height of absorbing aerosols with respect to cloud decks.

  20. Absorber for terahertz radiation management

    SciTech Connect

    Biallas, George Herman; Apeldoorn, Cornelis; Williams, Gwyn P.; Benson, Stephen V.; Shinn, Michelle D.; Heckman, John D.

    2015-12-08

    A method and apparatus for minimizing the degradation of power in a free electron laser (FEL) generating terahertz (THz) radiation. The method includes inserting an absorber ring in the FEL beam path for absorbing any irregular THz radiation and thus minimizes the degradation of downstream optics and the resulting degradation of the FEL output power. The absorber ring includes an upstream side, a downstream side, and a plurality of wedges spaced radially around the absorber ring. The wedges form a scallop-like feature on the innermost edges of the absorber ring that acts as an apodizer, stopping diffractive focusing of the THz radiation that is not intercepted by the absorber. Spacing between the scallop-like features and the shape of the features approximates the Bartlett apodization function. The absorber ring provides a smooth intensity distribution, rather than one that is peaked on-center, thereby eliminating minor distortion downstream of the absorber.

  1. Impact of the modal aerosol scheme GLOMAP-mode on aerosol forcing in the Hadley Centre Global Environmental Model

    NASA Astrophysics Data System (ADS)

    Bellouin, N.; Mann, G. W.; Woodhouse, M. T.; Johnson, C.; Carslaw, K. S.; Dalvi, M.

    2012-08-01

    The Hadley Centre Global Environmental Model (HadGEM) includes two aerosol schemes: the Coupled Large-scale Aerosol Simulator for Studies in Climate (CLASSIC), and the new Global Model of Aerosol Processes (GLOMAP-mode). GLOMAP-mode is a modal aerosol microphysics scheme that simulates not only aerosol mass but also aerosol number, represents internally-mixed particles, and includes aerosol microphysical processes such as nucleation. In this study, both schemes provide hindcast simulations of natural and anthropogenic aerosol species for the period 2000-2006. HadGEM simulations using GLOMAP-mode compare better than CLASSIC against a data-assimilated aerosol re-analysis and aerosol ground-based observations. GLOMAP-mode sulphate aerosol residence time is two days longer than CLASSIC sulphate aerosols, whereas black carbon residence time is much shorter. As a result, CLASSIC underestimates aerosol optical depths in continental regions of the Northern Hemisphere and likely overestimates absorption in remote regions. Aerosol direct and first indirect radiative forcings are computed from simulations of aerosols with emissions for the year 1850 and 2000. In 1850, GLOMAP-mode predicts lower aerosol optical depths and higher cloud droplet number concentrations than CLASSIC. Consequently, simulated clouds are much less susceptible to natural and anthropogenic aerosol changes when the microphysical scheme is used. In particular, the response of cloud condensation nuclei to an increase in dimethyl sulphide emissions becomes a factor of four smaller. The combined effect of different 1850 baselines, residence times, and cloud susceptibilities, leads to substantial differences in the aerosol forcings simulated by the two schemes. GLOMAP-mode finds a present-day direct aerosol forcing of -0.49 W m-2 on a global average, 72% stronger than the corresponding forcing from CLASSIC. This difference is compensated by changes in first indirect aerosol forcing: the forcing of -1.17 W m-2

  2. Corrosion resistant neutron absorbing coatings

    DOEpatents

    Choi, Jor-Shan [El Cerrito, CA; Farmer, Joseph C [Tracy, CA; Lee, Chuck K [Hayward, CA; Walker, Jeffrey [Gaithersburg, MD; Russell, Paige [Las Vegas, NV; Kirkwood, Jon [Saint Leonard, MD; Yang, Nancy [Lafayette, CA; Champagne, Victor [Oxford, PA

    2012-05-29

    A method of forming a corrosion resistant neutron absorbing coating comprising the steps of spray or deposition or sputtering or welding processing to form a composite material made of a spray or deposition or sputtering or welding material, and a neutron absorbing material. Also a corrosion resistant neutron absorbing coating comprising a composite material made of a spray or deposition or sputtering or welding material, and a neutron absorbing material.

  3. Corrosion resistant neutron absorbing coatings

    DOEpatents

    Choi, Jor-Shan; Farmer, Joseph C; Lee, Chuck K; Walker, Jeffrey; Russell, Paige; Kirkwood, Jon; Yang, Nancy; Champagne, Victor

    2013-11-12

    A method of forming a corrosion resistant neutron absorbing coating comprising the steps of spray or deposition or sputtering or welding processing to form a composite material made of a spray or deposition or sputtering or welding material, and a neutron absorbing material. Also a corrosion resistant neutron absorbing coating comprising a composite material made of a spray or deposition or sputtering or welding material, and a neutron absorbing material.

  4. Water absorbency by wool fibers: Hofmeister effect.

    PubMed

    Lo Nostro, Pierandrea; Fratoni, Laura; Ninham, Barry W; Baglioni, Piero

    2002-01-01

    Wool is a complex material, composed of cuticle and epicuticle cells, surrounded by a cell membrane complex. Wool fibers absorb moisture from air, and, once immersed in water, they take up considerable amounts of liquid. The water absorbency parameter can be determined from weight gain, according to a standard method, and used to quantify this phenomenon. In this paper we report a study on the water absorbency (or retention) of untreated wool fibers in the presence of aqueous 1 M salt solutions at 29 degrees C and a relative humidity of either 33% or 56%. The effect of anions was determined by selecting a wide range of different sodium salts, while the effect of cations was checked through some chlorides and nitrates. Our results show a significant specific ion and ion pair "Hofmeister" effects, that change the amount of water absorbed by the fibers. To understand this phenomenon, the water absorbency parameter (A(w)) is compared to different physicochemical parameters such as the lyotropic number, free energy of hydration of ions, molar surface tension increment, polarizability, refractive index increment, and molar refractivity. The data indicate that this Hofmeister phenomenon is controlled by dispersion forces that depend on the polarizability of ionic species, their adsorption frequencies, the solvent, and the substrate. These dispersion forces dominate the behavior in concentrated solutions. They are in accord with new developing theories of solutions and molecular interactions in colloidal systems that account for Hofmeister effects.

  5. Acquisition of in-situ and remote sensors for measurements of aerosols and chemical species. Final report, 12 December 1994-30 November 1996

    SciTech Connect

    Clarke, A.D.; Sharma, S.K.; Porter, J.N.

    1997-02-26

    Under this grant, the University of Hawaii has acquired instrumentation to relate remotely sensed lidar backscatter signals to both in situ measurements and to satellite derived radiances. These instruments include a turn key pulsed Nd:YAG and Ti-sapphire tunable laser transmitter and 12` lidar scanner, that are now part of SOEST scanning lidar system. The in situ characterization instrumentation package includes forward scattering spectrometer probe (FSSP), GPS receiver, and a portable satellite receiving station that would be deployed with lidar and in situ measurements to extend the range of observations and put these in broader context. These instruments are currently being used for studying coastal marine aerosols as a function of meteorological conditions on the island of Oahu.

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

    NASA Technical Reports Server (NTRS)

    Toon, Owen B.

    1994-01-01

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

  7. Thermodynamic characterization of Mexico City aerosol during MILAGRO 2006

    NASA Astrophysics Data System (ADS)

    Fountoukis, C.; Nenes, A.; Sullivan, A.; Weber, R.; Vanreken, T.; Fischer, M.; Matías, E.; Moya, M.; Farmer, D.; Cohen, R. C.

    2007-06-01

    Fast measurements of aerosol and gas-phase constituents coupled with the ISORROPIA-II thermodynamic equilibrium model are used to study the partitioning of semivolatile inorganic species and phase state of Mexico City aerosol sampled at the T1 site during the MILAGRO 2006 campaign. Overall, predicted semivolatile partitioning agrees well with measurements. PM2.5 is insensitive to changes in ammonia but is to acidic semivolatile species. Semi-volatile partitioning equilibrates on a timescale between 6 and 20 min. When the aerosol sulfate-to-nitrate molar ratio is less than 1, predictions improve substantially if the aerosol is assumed to follow the deliquescent phase diagram. Treating crustal species as "equivalent sodium" (rather than explicitly) in the thermodynamic equilibrium calculations introduces important biases in predicted aerosol water uptake, nitrate and ammonium; neglecting crustals further increases errors dramatically. This suggests that explicitly considering crustals in the thermodynamic calculations are required to accurately predict the partitioning and phase state of aerosols.

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

    NASA Astrophysics Data System (ADS)

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

    2015-11-01

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

  9. Long-term measurements of aerosol optical parameters in Athens, Greece

    NASA Astrophysics Data System (ADS)

    Paraskevopoulou, Despoina; Liakakou, Eleni; Gerasopoulos, Evangelos; Mihalopoulos, Nikolaos

    2015-04-01

    Aerosol chemical composition was studied in conjunction with its optical properties in the area of Athens Greece. For this purpose, sampling of fine aerosol fraction (PM2,5) took place on a daily basis from August 2010 to April 2013 at an urban background location. The samples are subsequently analyzed for their content in organic (OC) and elemental carbon (EC), major ions and trace metals, resulting in the exercise of chemical mass closure. In parallel, the optical properties of aerosols are recorded using a nephelometer and a particle soot absorption photometer (PSAP), leading to the calculation of scattering (σscat) and absorption (σabs) coefficients, respectively; while single scattering albedo (SSA) and mass scattering and absorption efficiencies are thereinafter calculated. Daily σscat values provide an average of 30.1±3.9 Μm-1 while, the average of σabs is 5.2±1.4 Μm-1. The seasonal cycle of σscat presents maximum during summer and in November, due to long-range transport of aerosol from continental Europe and dust transfer from Africa, respectively. The estimated mass absorption efficiency of EC is estimated to be 8.3±0.2 m2 g-1 for the whole studied period, while the corresponding estimated mass scattering efficiency of PM2.5 is 1.7±0.1 m2 g-1 and does not affected by the presence of dust. The average SSA equals to 0.87±0.11 for the three-year period. On a seasonal basis, SSA presents maximum values during summer that is consistent with the reduction of EC - the main absorbing specie. Finally, the reconstruction of scattering coefficients was performed taking into consideration the measured chemistry of fine aerosol.

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

    NASA Astrophysics Data System (ADS)

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

    2014-05-01

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

  11. Solar radiation absorbing material

    DOEpatents

    Googin, John M.; Schmitt, Charles R.; Schreyer, James M.; Whitehead, Harlan D.

    1977-01-01

    Solar energy absorbing means in solar collectors are provided by a solar selective carbon surface. A solar selective carbon surface is a microporous carbon surface having pores within the range of 0.2 to 2 micrometers. Such a surface is provided in a microporous carbon article by controlling the pore size. A thermally conductive substrate is provided with a solar selective surface by adhering an array of carbon particles in a suitable binder to the substrate, a majority of said particles having diameters within the range of about 0.2-10 microns.

  12. Global Atmospheric Aerosol Modeling

    NASA Technical Reports Server (NTRS)

    Hendricks, Johannes; Aquila, Valentina; Righi, Mattia

    2012-01-01

    Global aerosol models are used to study the distribution and properties of atmospheric aerosol particles as well as their effects on clouds, atmospheric chemistry, radiation, and climate. The present article provides an overview of the basic concepts of global atmospheric aerosol modeling and shows some examples from a global aerosol simulation. Particular emphasis is placed on the simulation of aerosol particles and their effects within global climate models.

  13. Aerosol Single-Scattering Albedo Derived from MODIS Reflectances over a Bright Surface

    NASA Astrophysics Data System (ADS)

    Wells, K. C.; Martins, J.; Remer, L. A.; Kreidenweis, S. M.; Stephens, G. L.

    2010-12-01

    The sign and magnitude of the aerosol radiative forcing over bright surfaces is highly dependent on the absorbing properties of the aerosol. Thus, the determination of aerosol forcing over desert regions requires accurate information about the aerosol single-scattering albedo (SSA). However, the brightness of desert surfaces complicates the retrieval of aerosol optical properties using passive space-based measurements. The aerosol critical reflectance is one parameter that can be used to relate TOA reflectance changes over land to the aerosol absorption properties, without knowledge of the underlying surface properties or aerosol loading. Physically, the parameter represents the TOA reflectance at which increased aerosol scattering due to increased aerosol loading is balanced by increased absorption of the surface contribution to the TOA reflectance. It can be derived by comparing two satellite images with different aerosol loading, assuming that the surface reflectance and background aerosol is similar between the two days. In this work, we explore the utility of the critical reflectance method for routine monitoring of spectral aerosol absorption from space over North Africa, a region that is predominantly impacted by absorbing dust and biomass burning aerosol. We derive the critical reflectance from MODIS Level 1B reflectances in the vicinity of two AERONET stations: Tamanrasset, a site in the Algerian Sahara, and Banizoumbou, a Sahelian site in Niger. We examine the sensitivity of the critical reflectance parameter to aerosol physical and optical properties, as well as solar and viewing geometry, using the SBDART model, and apply our findings to retrieve SSA from the MODIS critical reflectance values. We compare our results to AERONET-retrieved estimates, as well as measurements of the TOA albedo and surface fluxes from GERB, ARM, and CERES data. Spectral SSA values retrieved at Banizoumbou result in TOA forcing estimates that agree with CERES measurements

  14. Analysis of Ambient Aerosol Measurements During PROPHET 2001

    NASA Astrophysics Data System (ADS)

    Delia, A. E.; Garland, R.; Toohey, D. W.; Worsnop, D. R.; Allen, J. O.; Carroll, M. A.; Fortner, E.; Hengel, S.; Lilly, M.; Moody, J.; Huey, G.; Tanner, D.

    2002-12-01

    Aerosol size and composition were measured using an aerosol mass spectrometer, developed by Aerodyne Research, Inc., during PROPHET 2001 (Program for Research on Oxidants: PHotochemistry, Emissions and Transport). Our purpose in this study was to characterize chemical composition and size of ambient aerosols, investigate the effects of transport, and study aerosol microphysics. The site is located in a remote forested area of northern Michigan at the University of Michigan Biological Station, far from any large urban areas and surrounded primarily by deciduous forests. The aerosols at this site can be cataloged into four classes. The two principal classes are distinguished by meteorological conditions. Clean, northerly airflow produced low aerosol mass loadings dominated by organic species. More polluted southerly airflow brought higher aerosol mass loadings dominated by sulfate with an organic contribution. Under both of these conditions, aerosol existed almost entirely in the accumulation size mode of 300-600 nm. In addition to these principal aerosol types, small particle growth was observed on several occasions. It appears that these events occurred primarily during periods of low aerosol mass loading (i.e., northerly airflow) when the low aerosol number provided an opportunity for new particle formation and rapid growth. On at least one occasion, it appears that a large plume of sulfur dioxide that was converted to sulfuric acid near the site may be responsible for new particle formation. The fourth type of aerosol consisted of short events dominated by organic species, apparently diesel exhaust caused by local truck traffic. In addition to the overall aerosol characterization, comparisons with other measurements that affected the aerosol composition or characterized the air masses will be presented and the implications of these results for regional transport of aerosols will be discussed.

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

    SciTech Connect

    Paulson, S E

    2012-05-30

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

  16. Aerosol can puncture device test report

    SciTech Connect

    Leist, K.J.

    1994-10-01

    This test report documents the evaluation of an aerosol can puncture device to replace a system currently identified for use in the WRAP-1 facility. The new system is based upon a commercially available puncture device, as recommended by WHC Fire Protection. With modifications found necessary through the testing program, the Aerosol Can Puncture Device was found able to puncture and drain aerosol cans without incident. Modifications include the addition of a secondary collection bottle and the modification of the can puncture needle. In the course of testing, a variety of absorbents were tested to determine their performance in immobilizing drained fluids. The visibility of the puncture with Non-Destructive Examination techniques were also reviewed.

  17. Nitrogen-sulfur compounds in stratospheric aerosols

    NASA Technical Reports Server (NTRS)

    Farlow, N. H.; Snetsinger, K. G.; Hayes, D. M.; Lem, H. Y.; Tooper, B. M.

    1978-01-01

    Two forms of nitrosyl sulfuric acid (NOHSO4 and NOHS2O7) have been tentatively identified in stratospheric aerosols. The first of these can be formed either directly from gas reactions of NO2 with SO2 or by gas-particle interactions between NO2 and H2SO4. The second product may form when SO3 is involved. Estimates based on these reactions suggest that the maximum quantity of NO that might be absorbed in stratospheric aerosols could vary from one-third to twice the amount of NO in the surrounding air. If these reactions occur in the stratosphere, then a mechanism exists for removing nitrogen oxides from that region by aerosol particle fallout. This process may typify another natural means that helps cleanse the lower stratosphere of excessive pollutants.

  18. Atmospheric aerosol variability and properties in lowermost tropical free troposphere

    NASA Astrophysics Data System (ADS)

    Krejci, Radovan; Hamburger, Thomas; Ström, Johan; Tunved, Peter; Schmeissner, Tina; Matisans, Modris; Calderon, Silvia; Hoffman, Pedro

    2013-05-01

    The long-term measurements of aerosol number and size distributions in tropical free troposphere (FT) were carried out from 2007 until 2009. The measurements took place at the high altitude Atmospheric Research Station Pico Espejo located on top of the Sierra Nevada mountain ridge at 4765 m a.s.l. nearby the city of Mérida, Venezuela. Analysis of aerosol number concentration, size distribution and light absorbing aerosol focuses mainly on possible links to the atmospheric general circulation in the tropics and seasonality driven changes in biomass burning activity. Repeatable annual and diurnal cycles of the particle number concentration were observed.

  19. Aerosol gels

    NASA Technical Reports Server (NTRS)

    Sorensen, Christopher M. (Inventor); Chakrabarti, Amitabha (Inventor); Dhaubhadel, Rajan (Inventor); Gerving, Corey (Inventor)

    2010-01-01

    An improved process for the production of ultralow density, high specific surface area gel products is provided which comprises providing, in an enclosed chamber, a mixture made up of small particles of material suspended in gas; the particles are then caused to aggregate in the chamber to form ramified fractal aggregate gels. The particles should have a radius (a) of up to about 50 nm and the aerosol should have a volume fraction (f.sub.v) of at least 10.sup.-4. In preferred practice, the mixture is created by a spark-induced explosion of a precursor material (e.g., a hydrocarbon) and oxygen within the chamber. New compositions of matter are disclosed having densities below 3.0 mg/cc.

  20. Inferring aerosol types over the Indo-Gangetic Basin from ground based sunphotometer measurements

    NASA Astrophysics Data System (ADS)

    Srivastava, A. K.; Tripathi, S. N.; Dey, Sagnik; Kanawade, V. P.; Tiwari, S.

    2012-06-01

    A discrimination of aerosol types over the Indo-Gangetic Basin (IGB) region during pre-monsoon period was made using multi-year ground based sun/sky radiometer measured aerosol products associated with the size of aerosols and radiation absorptivity. High dust enriched aerosols (i.e. polluted dust, PD) were found to contribute more over the central IGB station at Kanpur (KNP, 62%) as compared to the eastern IGB station at Gandhi College (GC, 31%) whereas vice-versa was observed for polluted continental (PC) aerosols, which contain high anthropogenic and less dust aerosols. Contributions of carbonaceous particles having high absorbing (mostly black carbon, MBC) and low absorbing (mostly organic carbon, MOC) aerosols were found to be 11% and 10%, respectively at GC, which was ~ 46% and 62% higher than the observed contributions at KNP; however, very less contribution of non-absorbing (NA) aerosols was observed only at GC (2%). Variability in aerosol types together with single scattering albedo (SSA) at both the stations were also studied during the forenoon (FN) and afternoon (AN) hour, which suggests their strong association with emission sources. Results were well substantiated with the air mass back-trajectories and the fire products. Spectral information of SSA for each aerosol type discriminates the dominance of natural dust (SSA increases with increasing wavelength) with anthropogenic aerosols (SSA decreases with increasing wavelength) at both the locations. The estimated absorption Ångström exponent (AAE) values suggest relative dominance of absorbing type aerosols over the central part of IGB (due to dominant dust absorption) as compared to the eastern part during pre-monsoon period.

  1. Sensitivity of aerosol retrieval over snow surfaces

    NASA Astrophysics Data System (ADS)

    Seidel, F. C.; Painter, T. H.

    2011-12-01

    Significant amounts of black carbon and dust aerosols are transported to and accumulated in snowpacks of mountain ranges around the globe. The direct climate forcing of these particles is increasingly understood, whereas its indirect radiative forcing due to snow albedo and snow cover changes is still under investigation. In-situ and new remote sensing techniques are used to estimate snowpack properties from local to regional scales. Nevertheless, orbital and suborbital Earth observation data are difficult to analyze due to high spatial variability of the snowpack in rugged terrain. In addition, changes in atmospheric turbidity significantly complicate the estimation of snow cover characteristics and requires prior retrieval of optical and microphysical aerosol properties. Unfortunately, most aerosol retrieval techniques work only over dark surfaces. We therefore present a study on the sensitivity of aerosol optical depth (AOD) retrieval over snow surfaces. Radiative transfer calculations show that the sensitivity to surface spectral albedo depends strongly on the aerosol single scattering albedo (ratio of scattering efficiency to total extinction efficiency). Absorbing aerosol types (e.g. soot) provide a relatively good AOD retrieval sensitivity for very bright surfaces. The findings provide a basis for the development of future techniques and algorithms, which are able to concurrently retrieve snow and aerosol properties using remote sensing data. We explore these sensitivities with synthetic data and a time series of imaging spectrometer data, in situ spectral irradiance measurements, and sunphotometer measurements of AOD in the mountains of the Upper Colorado River Basin, USA. Ultimately, this research is important to map and better understand regional influences of aerosol and climate forcings on the cryosphere and water cycle in mountainous and other cold regions.

  2. Impact of Asian aerosols on air quality over the United States: A perspective from aerosol-cloud-radiation coupling

    NASA Astrophysics Data System (ADS)

    Tao, Z.; Yu, H.; Chin, M.

    2013-12-01

    It has well been established, through satellite/ground observations, that dust and aerosols from various Asian sources can travel across the Pacific and reach North America (NA) at least on episode bases. Once reaching NA, these inflow aerosols would compete with local emissions to influence atmospheric composition and air quality over the United States (US). The previous studies, typically based on one or multiple satellite measurements in combination with global/regional model simulations, suggest that the impact of Asian dust/aerosols on US air quality tend to be small since most inflow aerosols stay aloft. On the other hand, aerosols affect many key meteorological processes that will ultimately channel down to impact air quality. Aerosols absorb and scatter solar radiation that change the atmospheric stability, thus temperature, wind, and planetary boundary layer structure that would directly alter air quality. Aerosols can serve as cloud condensation nuclei and ice nuclei to modify cloud properties and precipitation that would also affect aerosol removal and concentration. This indirect impact of Asian aerosol inflow on US air quality may be substantial and need to be investigated. This study employs the NASA Unified WRF (NU-WRF) to address the question from the aerosol-radiation-cloud interaction perspective. The simulation period was selected from April to June of 2010 during which the Asian dust continuously reached NA based on CALIPSO satellite observation. The preliminary results show that the directly-transported Asian aerosol increases surface PM2.5 concentration by less than 2 μg/m3 over the west coast areas of US, and the aerosol-radiation-cloud feedback has a profound effect on air quality over the central to eastern US. A more detailed analysis links this finding to a series of meteorological conditions modified by aerosol effects.

  3. Liquid Cryogen Absorber for MICE

    SciTech Connect

    Baynham, D.E.; Bish, P.; Bradshaw, T.W.; Cummings, M.A.; Green,M.A.; Ishimoto, S.; Ivaniouchenkov, I.; Lau, W.; Yang, S.Q.; Zisman, M.S.

    2005-08-20

    The Muon Ionization Cooling Experiment (MICE) will test ionization cooling of muons. In order to have effective ionization cooling, one must use an absorber that is made from a low-z material. The most effective low z materials for ionization cooling are hydrogen, helium, lithium hydride, lithium and beryllium, in that order. In order to measure the effect of material on cooling, several absorber materials must be used. This report describes a liquid-hydrogen absorber that is within a pair of superconducting focusing solenoids. The absorber must also be suitable for use with liquid helium. The following absorber components are discussed in this report; the absorber body, its heat exchanger, the hydrogen system, and the hydrogen safety. Absorber cooling and the thin windows are not discussed here.

  4. Carbonaceous aerosols influencing atmospheric radiation: Black and organic carbon

    SciTech Connect

    Penner, J.E.

    1994-09-01

    Carbonaceous particles in the atmosphere may both scatter and absorb solar radiation. The fraction associated with the absorbing component is generally referred to as black carbon (BC) and is mainly produced from incomplete combustion processes. The fraction associated with condensed organic compounds is generally referred to as organic carbon (OC) or organic matter and is mainly scattering. Absorption of solar radiation by carbonaceous aerosols may heat the atmosphere, thereby altering the vertical temperature profile, while scattering of solar radiation may lead to a net cooling of the atmosphere/ocean system. Carbonaceous aerosols may also enhance the concentrations of cloud condensation nuclei. This paper summarizes observed concentrations of aerosols in remote continental and marine locations and provides estimates for the fine particle (D < 2.5 {mu}m) source rates of both OC and BC. The source rates for anthropogenic organic aerosols may be as large as the source rates for anthropogenic sulfate aerosols, suggesting a similar magnitude of direct forcing of climate. The role of BC in decreasing the amount of reflected solar radiation by OC and sulfates is discussed. The total estimated forcing depends on the source estimates for organic and black carbon aerosols which are highly uncertain. The role of organic aerosols acting as cloud condensation nuclei (CCN) is also described.

  5. Towards a Global Aerosol Climatology: Preliminary Trends in Tropospheric Aerosol Amounts and Corresponding Impact on Radiative Forcing between 1950 and 1990

    NASA Technical Reports Server (NTRS)

    Tegen, Ina; Koch, Dorothy; Lacis, Andrew A.; Sato, Makiko

    1999-01-01

    A global aerosol climatology is needed in the study of decadal temperature change due to natural and anthropogenic forcing of global climate change. A preliminary aerosol climatology has been developed from global transport models for a mixture of sulfate and carbonaceous aerosols from fossil fuel burning, including also contributions from other major aerosol types such as soil dust and sea salt. The aerosol distributions change for the period of 1950 to 1990 due to changes in emissions of SO2 and carbon particles from fossil fuel burning. The optical thickness of fossil fuel derived aerosols increased by nearly a factor of 3 during this period, with particularly strong increase in eastern Asia over the whole time period. In countries where environmental laws came into effect since the early 1980s (e.g. US and western Europe), emissions and consequently aerosol optical thicknesses did not increase considerably after 1980, resulting in a shift in the global distribution pattern over this period. In addition to the optical thickness, aerosol single scattering albedos may have changed during this period due to different trends in absorbing black carbon and reflecting sulfate aerosols. However, due to the uncertainties in the emission trends, this change cannot be determined with any confidence. Radiative forcing of this aerosol distribution is calculated for several scenarios, resulting in a wide range of uncertainties for top-of-atmosphere (TOA) forcings. Uncertainties in the contribution of the strongly absorbing black carbon aerosol leads to a range in TOA forcings of ca. -0.5 to + 0.1 Wm (exp. -2), while the change in aerosol distributions between 1950 to 1990 leads to a change of -0.1 to -0.3 Wm (exp. -2), for fossil fuel derived aerosol with a "moderate" contribution of black carbon aerosol.

  6. Aerosol typing - key information from aerosol studies

    NASA Astrophysics Data System (ADS)

    Mona, Lucia; Kahn, Ralph; Papagiannopoulos, Nikolaos; Holzer-Popp, Thomas; Pappalardo, Gelsomina

    2016-04-01

    Aerosol typing is a key source of aerosol information from ground-based and satellite-borne instruments. Depending on the specific measurement technique, aerosol typing can be used as input for retrievals or represents an output for other applications. Typically aerosol retrievals require some a priori or external aerosol type information. The accuracy of the derived aerosol products strongly depends on the reliability of these assumptions. Different sensors can make use of different aerosol type inputs. A critical review and harmonization of these procedures could significantly reduce related uncertainties. On the other hand, satellite measurements in recent years are providing valuable information about the global distribution of aerosol types, showing for example the main source regions and typical transport paths. Climatological studies of aerosol load at global and regional scales often rely on inferred aerosol type. There is still a high degree of inhomogeneity among satellite aerosol typing schemes, which makes the use different sensor datasets in a consistent way difficult. Knowledge of the 4d aerosol type distribution at these scales is essential for understanding the impact of different aerosol sources on climate, precipitation and air quality. All this information is needed for planning upcoming aerosol emissions policies. The exchange of expertise and the communication among satellite and ground-based measurement communities is fundamental for improving long-term dataset consistency, and for reducing aerosol type distribution uncertainties. Aerosol typing has been recognized as one of its high-priority activities of the AEROSAT (International Satellite Aerosol Science Network, http://aero-sat.org/) initiative. In the AEROSAT framework, a first critical review of aerosol typing procedures has been carried out. The review underlines the high heterogeneity in many aspects: approach, nomenclature, assumed number of components and parameters used for the

  7. Change in global aerosol composition since preindustrial times

    NASA Astrophysics Data System (ADS)

    Tsigaridis, K.; Krol, M.; Dentener, F. J.; Balkanski, Y.; Lathière, J.; Metzger, S.; Hauglustaine, D. A.; Kanakidou, M.

    2006-06-01

    To elucidate human induced changes of aerosol load and composition in the atmosphere, a coupled aerosol and gas-phase chemistry transport model of the troposphere and lower stratosphere has been used. This is the first 3-d modeling study that focuses on aerosol chemical composition change since preindustrial times considering the secondary organic aerosol formation together with all other main aerosol components including nitrate. In particular, we evaluate non-sea-salt sulfate (nss-SO4=), ammonium (NH4+), nitrate (NO3-), black carbon (BC), sea-salt, dust, primary and secondary organics (POA and SOA) with a focus on the importance of secondary organic aerosols. Our calculations show that the aerosol optical depth (AOD) has increased by about 21% since preindustrial times. This enhancement of AOD is attributed to a rise in the atmospheric load of BC, nss-SO4=, NO3-, POA and SOA by factors of 3.3, 2.6, 2.7, 2.3 and 1.2, respectively, whereas we assumed that the natural dust and sea-salt sources remained constant. The nowadays increase in carbonaceous aerosol loading is dampened by a 34-42% faster conversion of hydrophobic to hydrophilic carbonaceous aerosol leading to higher removal rates. These changes between the various aerosol components resulted in significant modifications of the aerosol chemical composition. The relative importance of the various aerosol components is critical for the aerosol climatic effect, since atmospheric aerosols behave differently when their chemical composition changes. According to this study, the aerosol composition changed significantly over the different continents and with height since preindustrial times. The presence of anthropogenically emitted primary particles in the atmosphere facilitates the condensation of the semi-volatile species that form SOA onto the aerosol phase, particularly in the boundary layer. The SOA burden that is dominated by the natural component has increased by 24% while its contribution to the AOD has

  8. Change in global aerosol composition since preindustrial times

    NASA Astrophysics Data System (ADS)

    Tsigaridis, K.; Krol, M.; Dentener, F. J.; Balkanski, Y.; Lathière, J.; Metzger, S.; Hauglustaine, D. A.; Kanakidou, M.

    2006-11-01

    To elucidate human induced changes of aerosol load and composition in the atmosphere, a coupled aerosol and gas-phase chemistry transport model of the troposphere and lower stratosphere has been used. The present 3-D modeling study focuses on aerosol chemical composition change since preindustrial times considering the secondary organic aerosol formation together with all other main aerosol components including nitrate. In particular, we evaluate non-sea-salt sulfate (nss-SO4=), ammonium (NH4+), nitrate (NO3-), black carbon (BC), sea-salt, dust, primary and secondary organics (POA and SOA) with a focus on the importance of secondary organic aerosols. Our calculations show that the aerosol optical depth (AOD) has increased by about 21% since preindustrial times. This enhancement of AOD is attributed to a rise in the atmospheric load of BC, nss-SO4=, NO3aerosol loading is dampened by a 34-42% faster conversion of hydrophobic to hydrophilic carbonaceous aerosol leading to higher removal rates. These changes between the various aerosol components resulted in significant modifications of the aerosol chemical composition. The relative importance of the various aerosol components is critical for the aerosol climatic effect, since atmospheric aerosols behave differently when their chemical composition changes. According to this study, the aerosol composition changed significantly over the different continents and with height since preindustrial times. The presence of anthropogenically emitted primary particles in the atmosphere facilitates the condensation of the semi-volatile species that form SOA onto the aerosol phase, particularly in the boundary layer. The SOA burden that is dominated by the natural component has increased by 24% while its contribution to the AOD has increased

  9. Differentiation of hydrophobic from hydrophilic submicrometer aerosol particles

    SciTech Connect

    Juozaitis, A.; Ulevicius, V.; Girgzdys, A. ); Willeke, K. )

    1993-02-01

    A method has been developed that differentiates hydrophobic from hydrophilic submicrometer aerosol particles in air environments containing polydisperse aerosols composed of different chemical species. First, a narrow particle size range is extracted from the polydisperse aerosol by an electrostatic aerosol classifier. Then the monodisperse aerosols of different origins are exposed to preselected supersaturation levels and are size-classified again by a second electrostatic classifier. Hydrophobic aerosol particles pass through the second classifier when its size window matches that of the first classifier. Hydrophilic aerosol particles grow to a larger size and are removed by the second classifier. The method has been applied in the field by measuring the fraction of hydrophobic atmospheric particles in a suburb of Vilnius, Lithuania, during a period of high emission of hydrophobic soot particles from residential coal and industrial oil burning in winter. 33 refs., 4 figs.

  10. Parameter sensitivity study of Arctic aerosol vertical distribution in CAM5

    NASA Astrophysics Data System (ADS)

    Jiao, C.; Flanner, M.

    2015-12-01

    Arctic surface temperature response to light-absorbing aerosols (black carbon, brown carbon and dust) depends strongly on their vertical distributions. Improving model simulations of three dimensional aerosol fields in the remote Arctic region will therefore lead to improved projections of the climate change caused by aerosol emissions. In this study, we investigate how different physical parameterizations in the Community Atmosphere Model version 5 (CAM5) influence the simulated vertical distribution of Arctic aerosols. We design experiments to test the sensitivity of the simulated aerosol fields to perturbations of selected aerosol process-related parameters in the Modal Aerosol Module with seven lognormal modes (MAM7), such as those govern aerosol aging, in-cloud and below-cloud scavenging, aerosol hygroscopicity and so on. The simulations are compared with observed aerosol vertical distributions and total optical depth to assess model performance and quantify uncertainties associated with these model parameterizations. Observations applied here include Arctic aircraft measurements of black carbon and sulfate vertical profiles, along with Aerosol Robotic Network (AERONET) optical depth measurements. We also assess the utility of using High Spectral Resolution Lidar (HSRL) measurements from the ARM Barrow site to infer vertical profiles of aerosol extinction. The sensitivity study explored here will provide guidance for optimizing global aerosol simulations.

  11. Ferroelectrics based absorbing layers

    NASA Astrophysics Data System (ADS)

    Hao, Jianping; Sadaune, Véronique; Burgnies, Ludovic; Lippens, Didier

    2014-07-01

    We show that ferroelectrics-based periodic structure made of BaSrTiO3 (BST) cubes, arrayed onto a metal plate with a thin dielectric spacer film exhibit a dramatic enhancement of absorbance with value close to unity. The enhancement is found around the Mie magnetic resonance of the Ferroelectrics cubes with the backside metal layer stopping any transmitted waves. It also involves quasi-perfect impedance matching resulting in reflection suppression via simultaneous magnetic and electrical activities. In addition, it was shown numerically the existence of a periodicity optimum, which is explained from surface waves analysis along with trade-off between the resonance damping and the intrinsic loss of ferroelectrics cubes. An experimental verification in a hollow waveguide configuration with a good comparison with full-wave numerical modelling is at last reported by measuring the scattering parameters of single and dual BST cubes schemes pointing out coupling effects for densely packed structures.

  12. Dual broadband metamaterial absorber.

    PubMed

    Kim, Young Ju; Yoo, Young Joon; Kim, Ki Won; Rhee, Joo Yull; Kim, Yong Hwan; Lee, YoungPak

    2015-02-23

    We propose polarization-independent and dual-broadband metamaterial absorbers at microwave frequencies. This is a periodic meta-atom array consisting of metal-dielectric-multilayer truncated cones. We demonstrate not only one broadband absorption from the fundamental magnetic resonances but additional broadband absorption in high-frequency range using the third-harmonic resonance, by both simulation and experiment. In simulation, the absorption was over 90% in 3.93-6.05 GHz, and 11.64-14.55 GHz. The corresponding experimental absorption bands over 90% were 3.88-6.08 GHz, 9.95-10.46 GHz and 11.86-13.84 GHz, respectively. The origin of absorption bands was elucidated. Furthermore, it is independent of polarization angle owing to the multilayered circular structures. The design is scalable to smaller size for the infrared and the visible ranges.

  13. THz-metamaterial absorbers

    NASA Astrophysics Data System (ADS)

    Tuong Pham, Van; Park, J. W.; Vu, Dinh Lam; Zheng, H. Y.; Rhee, J. Y.; Kim, K. W.; Lee, Y. P.

    2013-03-01

    An ultrabroad-band metamaterial absorber was investigated in mid-IR regime based on a similar model in previous work. The high absorption of metamaterial was obtained in a band of 8-11.7 THz with energy loss distributed in SiO2, which is appropriate potentially for solar-cell applications. A perfect absorption peak was provided by using a sandwich structure with periodical anti-dot pattern in the IR region, getting closed to visible-band metamaterials. The dimensional parameters were examined for the corresponding fabrication. Invited talk at the 6th International Workshop on Advanced Materials Science and Nanotechnology, 30 October-2 November, 2012, Ha Long, Vietnam.

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

    NASA Astrophysics Data System (ADS)

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

    2016-04-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2015-12-01

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

  16. Aerosol types and radiative forcing estimates over East Asia

    NASA Astrophysics Data System (ADS)

    Bhawar, Rohini L.; Lee, Woo-Seop; Rahul, P. R. C.

    2016-09-01

    Using the CALIPSO (Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observations) and MODIS (Moderate Resolution Imaging Spectroradiometer) satellite data sets along with the CSIRO-MK 3.6.0 model simulations, we analyzed the aerosol optical depth (AOD) variability during March-May (MAM), June-August (JJA) along with their annual mean variability over East Asia for the period 2006-2012. The CALIPSO measurements correlated well with the MODIS measurements and the CSIRO-MK 3.6.0 model simulations over the spatial distribution patterns of the aerosols, but CALIPSO underestimated the magnitudes of the AOD. Maximum smoke aerosol loading is observed to occur during JJA, as a result of wind transport from Southern China while dust loading dominated during MAM via the transport from desert region. The vertical distribution profiles revealed that there is uniform distribution of smoke aerosols during both MAM and JJA, only differing at the altitude at which they peak; while the dust aerosols during MAM showed a significant distribution from the surface to 10 km altitude and JJA was marked with lower dust loading at the same altitudes. Both dust and smoke aerosols warm the atmosphere in MAM but due to the absorbing nature of smoke aerosols, they cause considerable cooling at the surface which is double when compared to the dust aerosols. The top of the atmosphere aerosol radiative forcing (ARF) due to smoke and dust aerosols is positive in MAM which indicates warming over East Asia. During MAM a consistent declining trend of the surface ARF due to smoke aerosols persisted over the last three decades as conspicuously evidenced from model analysis; the decline is ∼10 W/m2 from 1980 to 2012.

  17. Aqueous Chemistry in the Clouds of Venus: A Possible Source for the UV Absorber

    NASA Astrophysics Data System (ADS)

    Baines, Kevin H.; Delitsky, M. L.

    2013-10-01

    The identity and cause of the UV absorber near the Venusian cloudtops 62-70 km altitude) has been an enduring mystery. Given the role of sulfur in Venus’s atmosphere, where, somewhat analogous to water on Earth, it cycles through gas, liquid, and (possibly) solid phases in the atmosphere, it has been a prime suspect as at least a key component, perhaps as long-lived solid poly-sulfur aerosols, Sn, where n > 4. However, the narrow range of altitudes inhabited by the UV absorber (thought to form and reside primarily above 62 km altitude) seems incompatible with Sn, which should vertically disperse after formation. Here, we point to another process that could lead to somewhat more exotic chemistries that favor formation and sequestration at high altitudes: Aqueous chemistry within H2SO4-nH2O cloud particles. Due to (1) the decrease of temperature and (2) the increase in the fraction of water (“n” in the previous formula) of each cloud droplet with altitude, high-altitude particles near the cloudtops are - via the “heterogeneous uptake” process - significantly more capable of capturing and concentrating trace gases, in particular HCl. For example, the heterogeneous uptake of HCl in H2SO4 droplets near the 65-km cloudtops is at least three times greater than that found in the middle of the clouds near 55 km altitude. Other factors such as local mixing ratios and the concentration of other solvents in the droplet also modify the uptake. Within the cloud droplets, solution chemistry between HCl and H2SO4 may lead to the formation of chlorosulfonic acid, ClSO3H, which is a weak acid that readily breaks down into other species, such as SO2Cl2 (sulfuryl chloride) and SOCl2 (thionyl chloride). Together, these three materials have UV-blue absorptions at 0.21, 0.29, 0.39 and 0.47 micron. Thus, H2SO4 aerosols at high altitudes may take on lasting UV absorption characteristics, dependent on temperature (altitude) and other conditions, Balloons floating at benign Earth

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

    NASA Astrophysics Data System (ADS)

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

    2013-01-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2013-04-01

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

  20. Electrochemically regenerable carbon dioxide absorber

    NASA Technical Reports Server (NTRS)

    Woods, R. R.; Marshall, R. D.; Schubert, F. H.; Heppner, D. B.

    1979-01-01

    Preliminary designs were generated for two electrochemically regenerable carbon dioxide absorber concepts. Initially, an electrochemically regenerable absorption bed concept was designed. This concept incorporated the required electrochemical regeneration components in the absorber design, permitting the absorbent to be regenerated within the absorption bed. This hardware was identified as the electrochemical absorber hardware. The second hardware concept separated the functional components of the regeneration and absorption process. This design approach minimized the extravehicular activity component volume by eliminating regeneration hardware components within the absorber. The electrochemical absorber hardware was extensively characterized for major operating parameters such as inlet carbon dioxide partial pressure, process air flow rate, operational pressure, inlet relative humidity, regeneration current density and absorption/regeneration cycle endurance testing.

  1. Broadband patterned magnetic microwave absorber

    SciTech Connect

    Li, Wei; Wu, Tianlong; Wang, Wei; Guan, Jianguo; Zhai, Pengcheng

    2014-07-28

    It is a tough task to greatly improve the working bandwidth for the traditional flat microwave absorbers because of the restriction of available material parameters. In this work, a simple patterning method is proposed to drastically broaden the absorption bandwidth of a conventional magnetic absorber. As a demonstration, an ultra-broadband microwave absorber with more than 90% absorption in the frequency range of 4–40 GHz is designed and experimentally realized, which has a thin thickness of 3.7 mm and a light weight equivalent to a 2-mm-thick flat absorber. In such a patterned absorber, the broadband strong absorption is mainly originated from the simultaneous incorporation of multiple λ/4 resonances and edge diffraction effects. This work provides a facile route to greatly extend the microwave absorption bandwidth for the currently available absorbing materials.

  2. Liquid Hydrogen Absorber for MICE

    SciTech Connect

    Ishimoto, S.; Suzuki, S.; Yoshida, M.; Green, Michael A.; Kuno, Y.; Lau, Wing

    2010-05-30

    Liquid hydrogen absorbers for the Muon Ionization Cooling Experiment (MICE) have been developed, and the first absorber has been tested at KEK. In the preliminary test at KEK we have successfully filled the absorber with {approx}2 liters of liquid hydrogen. The measured hydrogen condensation speed was 2.5 liters/day at 1.0 bar. No hydrogen leakage to vacuum was found between 300 K and 20 K. The MICE experiment includes three AFC (absorber focusing coil) modules, each containing a 21 liter liquid hydrogen absorber made of aluminum. The AFC module has safety windows to separate its vacuum from that of neighboring modules. Liquid hydrogen is supplied from a cryocooler with cooling power 1.5 W at 4.2 K. The first absorber will be assembled in the AFC module and installed in MICE at RAL.

  3. Measurements of nitric acid, carboxylic acids, and selected aerosol species for the NASA/GTE Pacific Mission - West (PEM-WEST)

    NASA Technical Reports Server (NTRS)

    Talbot, Robert W.; Dibb, Jack E.

    1993-01-01

    The research investigation funded through this grant to the University of New Hampshire was performed during a major field expedition conducted by the NASA Tropospheric Chemistry Program. The NASA Global Tropospheric Experiment (GTE) executed an airborne science mission (PEM-WEST A) aboard the NASA Ames DC-8 over the Pacific Ocean during Sep./Oct. 1981. The atmosphere over the central Pacific Ocean is the only major region in the Northern Hemisphere that is relatively free from direct anthropogenic influence. Thus, this environment is ideally suited to study the natural biogeochemical cycles of carbon, nitrogen, ozone, sulfur, and aerosols without serious confounding problems related to anthropogenic emissions. Asian sources account for about 17 percent of the global budgets of nitrogen oxides (NO(x)) and sulfur dioxide (SO2). The Pacific Rim region therefore provides the opportunity to study the anthropogenic impact on natural atmospheric chemical cycles. The PEM-WEST A flights were focused on contrasting the chemistry of 'clean' air over the central Pacific with anthropogenically impacted air advected off the Asian continent. The principal objectives of PEM-WEST A were to investigate the atmospheric chemistry of ozone (O3) and its precursors, and to study important aspects of the atmospheric sulfur cycle over the western Pacific Ocean. Measurements conducted by the University of New Hampshire contributed directly to both of these objectives. Subsequent PEM-WEST field missions are planned by GTE in the mid-1990's to contrast atmospheric chemistry documented during PEM-WEST A with other time periods. This report presents preliminary findings from the PEM-WEST A field mission. Data interpretation is currently ongoing with the goal of manuscript submission of scientific results to a special issue of the Journal of Geophysical Research-Atmospheres in Feb. 1994. The reader is strongly encouraged to review this suite of profession articles to appreciate the overall

  4. Impact of Tropospheric Aerosol Absorption on Ozone Retrieval from buv Measurements

    NASA Technical Reports Server (NTRS)

    Torres, O.; Bhartia, P. K.

    1998-01-01

    The impact of tropospheric aerosols on the retrieval of column ozone amounts using spaceborne measurements of backscattered ultraviolet radiation is examined. Using radiative transfer calculations, we show that uv-absorbing desert dust may introduce errors as large as 10% in ozone column amount, depending on the aerosol layer height and optical depth. Smaller errors are produced by carbonaceous aerosols that result from biomass burning. Though the error is produced by complex interactions between ozone absorption (both stratospheric and tropospheric), aerosol scattering, and aerosol absorption, a surprisingly simple correction procedure reduces the error to about 1%, for a variety of aerosols and for a wide range of aerosol loading. Comparison of the corrected TOMS data with operational data indicates that though the zonal mean total ozone derived from TOMS are not significantly affected by these errors, localized affects in the tropics can be large enough to seriously affect the studies of tropospheric ozone that are currently undergoing using the TOMS data.

  5. AEROSOL AND GAS MEASUREMENT

    EPA Science Inventory

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

  6. Climate Implications of the Heterogeneity of Anthropogenic Aerosol Forcing

    NASA Astrophysics Data System (ADS)

    Persad, Geeta Gayatri

    Short-lived anthropogenic aerosols are concentrated in regions of high human activity, where they interact with radiation and clouds, causing horizontally heterogeneous radiative forcing between polluted and unpolluted regions. Aerosols can absorb shortwave energy in the atmosphere, but deplete it at the surface, producing opposite radiative perturbations between the surface and atmosphere. This thesis investigates climate and policy implications of this horizontal and vertical heterogeneity of anthropogenic aerosol forcing, employing the Geophysical Fluid Dynamics Laboratory's AM2.1 and AM3 models, both at a global scale and using East Asia as a regional case study. The degree of difference between spatial patterns of climate change due to heterogeneous aerosol forcing versus homogeneous greenhouse gas forcing deeply impacts the detection, attribution, and prediction of regional climate change. This dissertation addresses a gap in current understanding of these two forcings' response pattern development, using AM2.1 historical forcing simulations. The results indicate that fast atmospheric and land-surface processes alone substantially homogenize the global pattern of surface energy flux response to heterogeneous aerosol forcing. Aerosols' vertical redistribution of energy significantly impacts regional climate, but is incompletely understood. It is newly identified here, via observations and historical and idealized forcing simulations, that increased aerosol-driven atmospheric absorption may explain half of East Asia's recent surface insolation decline. Further, aerosols' surface and atmospheric effects counteract each other regionally---atmospheric heating enhances summer monsoon circulation, while surface dimming suppresses it---but absorbing aerosols' combined effects reduce summer monsoon rainfall. This thesis constitutes the first vertical decomposition of aerosols' impacts in this high-emissions region and elucidates the monsoonal response to aerosols

  7. Easy Aerosol - a model intercomparison project to study aerosol-radiative interactions and their impact on regional climate

    NASA Astrophysics Data System (ADS)

    Voigt, A.; Bony, S.; Stevens, B. B.; Boucher, O.; Medeiros, B.; Pincus, R.; Wang, Z.; Zhang, K.; Lewinschal, A.; Bellouin, N.; Yang, Y. M.

    2015-12-01

    Recent studies illustrated the potential of aerosols to change the large-scale atmospheric circulation and precipitation patterns, but it remains unclear to what extent the proposed aerosol-induced changes reflect robust model behavior and are affected by the climate system's internal variability. "Easy Aerosol" addresses this question by subjecting nine comprehensive climate models with prescribed sea-surface temperatures (SSTs) to the same set of idealized "easy" aerosol perturbations. The aerosol perturbations are designed based on a global aerosol climatology and mimic the gravest mode of the anthropogenic aerosol. They both scatter and absorb shortwave radiation, but to focus on direct radiative effects aerosol-cloud interactions are omitted. Each model contributes seven simulations. A clean control case with no aerosol-radiative effects is compared to six perturbed simulations with differing aerosol loading, zonal aerosol distributions, and SSTs. To estimate the role of internal variability, one of the models contributes a 5-member ensemble for each simulation. When observed SSTs from years 1979-2005 are used, the aerosol leads to a local depression of precipitation at the Northern Hemisphere center of the aerosol and a northward shift of the intertropical convergence zone (ITCZ). This is consistent with the aerosol's shortwave atmospheric heating and the fact that SSTs are fixed. Moreover, the Northern hemisphere mid-latitude jet shifts poleward in the annual and zonal-mean. Due to large natura variability, however, these signals only emerge in ensemble runs or if the aerosol optical depth is increased by a factor of five compared to the observed magnitude of the present-day anthropogenic aerosol. When SSTs are adapted to include the cooling effect of the aerosol, the ITCZ and the Northern hemisphere jet shift southward in the annual and zonal-mean. The models exhibit very similar precipitation and zonal wind changes in response to the SST change, showing

  8. Condensing Organic Aerosols in a Microphysical Model

    NASA Astrophysics Data System (ADS)

    Gao, Y.; Tsigaridis, K.; Bauer, S.

    2015-12-01

    The condensation of organic aerosols is represented in a newly developed box-model scheme, where its effect on the growth and composition of particles are examined. We implemented the volatility-basis set (VBS) framework into the aerosol mixing state resolving microphysical scheme Multiconfiguration Aerosol TRacker of mIXing state (MATRIX). This new scheme is unique and advances the representation of organic aerosols in models in that, contrary to the traditional treatment of organic aerosols as non-volatile in most climate models and in the original version of MATRIX, this new scheme treats them as semi-volatile. Such treatment is important because low-volatility organics contribute significantly to the growth of particles. The new scheme includes several classes of semi-volatile organic compounds from the VBS framework that can partition among aerosol populations in MATRIX, thus representing the growth of particles via condensation of low volatility organic vapors. Results from test cases representing Mexico City and a Finish forrest condistions show good representation of the time evolutions of concentration for VBS species in the gas phase and in the condensed particulate phase. Emitted semi-volatile primary organic aerosols evaporate almost completely in the high volatile range, and they condense more efficiently in the low volatility range.

  9. Cloud Forming Potential of Aminium Carboxylate Aerosols

    NASA Astrophysics Data System (ADS)

    Gomez Hernandez, M. E.; McKeown, M.; Taylor, N.; Collins, D. R.; Lavi, A.; Rudich, Y.; Zhang, R.

    2014-12-01

    Atmospheric aerosols affect visibility, air quality, human health, climate, and in particular the aerosol direct and indirect forcings represent the largest uncertainty in climate projections. In this paper, we present laboratory measurements of the hygroscopic growth factors (HGf) and cloud condensation nuclei (CCN) activity of a series of aminium carboxylate salt aerosols, utilizing a Hygroscopicity Tandem Differential Mobility Analyzer (HTDMA) coupled to a Condensation Particle Counter (CPC) and a CCN counter. HGf measurements were conducted for size-selected aerosols with diameters ranging from 46 nm to 151 nm and at relative humidity (RH%) values ranging from 10 to 90%. In addition, we have calculated the CCN activation diameters for the aminium carboxylate aerosols and derived the hygroscopicity parameter (k or kappa) values for all species using three methods, i.e., the mixing rule approximation, HGf, and CCN results. Our results show that variations in the ratio of acid to base directly affect the activation diameter, HGf, and (k) values of the aminium carboxylate aerosols. Atmospheric implications of the variations in the chemical composition of aminium carboxylate aerosols on their cloud forming potential will be discussed.

  10. On the implications of aerosol liquid water and phase separation for organic aerosol mass

    NASA Astrophysics Data System (ADS)

    Pye, Havala O. T.; Murphy, Benjamin N.; Xu, Lu; Ng, Nga L.; Carlton, Annmarie G.; Guo, Hongyu; Weber, Rodney; Vasilakos, Petros; Wyat Appel, K.; Hapsari Budisulistiorini, Sri; Surratt, Jason D.; Nenes, Athanasios; Hu, Weiwei; Jimenez, Jose L.; Isaacman-VanWertz, Gabriel; Misztal, Pawel K.; Goldstein, Allen H.

    2017-01-01

    Organic compounds and liquid water are major aerosol constituents in the southeast United States (SE US). Water associated with inorganic constituents (inorganic water) can contribute to the partitioning medium for organic aerosol when relative humidities or organic matter to organic carbon (OM / OC) ratios are high such that separation relative humidities (SRH) are below the ambient relative humidity (RH). As OM / OC ratios in the SE US are often between 1.8 and 2.2, organic aerosol experiences both mixing with inorganic water and separation from it. Regional chemical transport model simulations including inorganic water (but excluding water uptake by organic compounds) in the partitioning medium for secondary organic aerosol (SOA) when RH > SRH led to increased SOA concentrations, particularly at night. Water uptake to the organic phase resulted in even greater SOA concentrations as a result of a positive feedback in which water uptake increased SOA, which further increased aerosol water and organic aerosol. Aerosol properties, such as the OM / OC and hygroscopicity parameter (κorg), were captured well by the model compared with measurements during the Southern Oxidant and Aerosol Study (SOAS) 2013. Organic nitrates from monoterpene oxidation were predicted to be the least water-soluble semivolatile species in the model, but most biogenically derived semivolatile species in the Community Multiscale Air Quality (CMAQ) model were highly water soluble and expected to contribute to water-soluble organic carbon (WSOC). Organic aerosol and SOA precursors were abundant at night, but additional improvements in daytime organic aerosol are needed to close the model-measurement gap. When taking into account deviations from ideality, including both inorganic (when RH > SRH) and organic water in the organic partitioning medium reduced the mean bias in SOA for routine monitoring networks and improved model performance compared to observations from SOAS. Property updates from

  11. Light absorption properties of water soluble organic aerosol from Residential Wood Burning in Fresno, CA: Results from 2013 NASA DISCOVER-AQ Campaign

    NASA Astrophysics Data System (ADS)

    Kim, H.; Zhang, Q.; Young, D. E.; Parworth, C.

    2015-12-01

    Light absorption properties of water soluble organic aerosol were investigated at Fresno, CA from 13 January to 11 February, 2013 as part of the NASA DISCOVER-AQ campaign. The light absorption spectra of water soluble organic aerosol in PM2.5 was measured using a UV/vis diode array detector (DAD) coupled with a particle into liquid sampler (PILS) that sampled downstream of a PM2.5 cyclone (URG). The PILS was also coupled with two ion chromatographs (IC) to measure inorganic and organic ionic species in PM2.5. In addition, an Aerodyne High Resolution Time-of-Flight Aerosol Mass Spectrometer (HR-ToF-AMS) was deployed at the same site to measure size-resolved chemical composition of submicrometer aerosol (PM1) in real time during this study. Light absorption at 365 nm (Abs365), which is typically used as a proxy of water-soluble brown carbon (BrC), showed strong enhancement during night time and appeared to correlate well (r = 0.71) with biomass burning organic aerosol (BBOA) from residential wood burning for heating in the Fresno area. The tight correlations between Abs365 and biomass burning relevant tracers such as acetonitrile (r = 0.69), AMS-signature ions for phenolic compounds (r = 0.52-0.71), PAH (r = 0.74), and potassium (r = 0.67) further confirm that biomass burning contributed significantly to water soluble brown carbon during this study. The absorption angstrom exponent (Åa) values fitted between 300 and 700 nm wavelength were 3.3 ± 1.1, 2.0 ± 0.9 and 4.0 ± 0.8, respectively, in the morning, afternoon and nighttime, indicating that BrC is prevalent at night in Fresno during wintertime. However, there are also indications that small amount of BrC existed during the daytime as well, likely due to daytime wood burning and other sources such as the formation of light-absorbing secondary organic aerosol (SOA). Finally, light absorption at 300 nm, 330 nm, and 390 nm were found to correlate tightly with BBOA, which indicate that biomass burning also emits

  12. Aerosol distribution apparatus

    DOEpatents

    Hanson, W.D.

    An apparatus for uniformly distributing an aerosol to a plurality of filters mounted in a plenum, wherein the aerosol and air are forced through a manifold system by means of a jet pump and released into the plenum through orifices in the manifold. The apparatus allows for the simultaneous aerosol-testing of all the filters in the plenum.

  13. Improved solid aerosol generator

    DOEpatents

    Prescott, D.S.; Schober, R.K.; Beller, J.

    1988-07-19

    An improved solid aerosol generator used to produce a gas borne stream of dry, solid particles of predetermined size and concentration. The improved solid aerosol generator nebulizes a feed solution of known concentration with a flow of preheated gas and dries the resultant wet heated aerosol in a grounded, conical heating chamber, achieving high recovery and flow rates. 2 figs.

  14. Solid aerosol generator

    DOEpatents

    Prescott, Donald S.; Schober, Robert K.; Beller, John

    1992-01-01

    An improved solid aerosol generator used to produce a gas borne stream of dry, solid particles of predetermined size and concentration. The improved solid aerosol generator nebulizes a feed solution of known concentration with a flow of preheated gas and dries the resultant wet heated aerosol in a grounded, conical heating chamber, achieving high recovery and flow rates.

  15. Solid aerosol generator

    DOEpatents

    Prescott, D.S.; Schober, R.K.; Beller, J.

    1992-03-17

    An improved solid aerosol generator used to produce a gas borne stream of dry, solid particles of predetermined size and concentration is disclosed. The improved solid aerosol generator nebulizes a feed solution of known concentration with a flow of preheated gas and dries the resultant wet heated aerosol in a grounded, conical heating chamber, achieving high recovery and flow rates. 2 figs.

  16. Energy absorber for the CETA

    NASA Technical Reports Server (NTRS)

    Wesselski, Clarence J.

    1994-01-01

    The energy absorber that was developed for the CETA (Crew Equipment and Translation Aid) on Space Station Freedom is a metal on metal frictional type and has a load regulating feature that prevents excessive stroking loads from occurring while in operation. This paper highlights some of the design and operating aspects and the testing of this energy absorber.

  17. Improvement Of The Helmholtz Absorber

    NASA Technical Reports Server (NTRS)

    Morrow, Duane L.

    1992-01-01

    Helmholtz-resonator system improved to enable it to absorb sound at more than one frequency without appreciable loss of effectiveness at primary frequency. Addition of annular cavities enables absorption of sound at harmonic frequencies in addition to primary frequency. Improved absorber designed for use on structures of high transmission loss. Applied to such machines as fixed-speed engines and fans.

  18. Metal-shearing energy absorber

    NASA Technical Reports Server (NTRS)

    Fay, R. J.; Wittrock, E. P.

    1971-01-01

    Device, consisting of tongue of thin aluminum alloy strip, pull tab, slotted steel plate which serves as cutter, and steel buckle, absorbs mechanical energy when its ends are subjected to tensile loading. Device is applicable as auxiliary shock absorbing anchor for automobile and airplane safety belts.

  19. Aerosol Radiative Forcing and Weather Forecasts in the ECMWF Model

    NASA Astrophysics Data System (ADS)

    Bozzo, A.; Benedetti, A.; Rodwell, M. J.; Bechtold, P.; Remy, S.

    2015-12-01

    Aerosols play an important role in the energy balance of the Earth system via direct scattering and absorpiton of short-wave and long-wave radiation and indirect interaction with clouds. Diabatic heating or cooling by aerosols can also modify the vertical stability of the atmosphere and influence weather pattern with potential impact on the skill of global weather prediction models. The Copernicus Atmosphere Monitoring Service (CAMS) provides operational daily analysis and forecast of aerosol optical depth (AOD) for five aerosol species using a prognostic model which is part of the Integrated Forecasting System of the European Centre for Medium-Range Weather Forecasts (ECMWF-IFS). The aerosol component was developed during the research project Monitoring Atmospheric Composition and Climate (MACC). Aerosols can have a large impact on the weather forecasts in case of large aerosol concentrations as found during dust storms or strong pollution events. However, due to its computational burden, prognostic aerosols are not yet feasible in the ECMWF operational weather forecasts, and monthly-mean climatological fields are used instead. We revised the aerosol climatology used in the operational ECMWF IFS with one derived from the MACC reanalysis. We analyse the impact of changes in the aerosol radiative effect on the mean model climate and in medium-range weather forecasts, also in comparison with prognostic aerosol fields. The new climatology differs from the previous one by Tegen et al 1997, both in the spatial distribution of the total AOD and the optical properties of each aerosol species. The radiative impact of these changes affects the model mean bias at various spatial and temporal scales. On one hand we report small impacts on measures of large-scale forecast skill but on the other hand details of the regional distribution of aerosol concentration have a large local impact. This is the case for the northern Indian Ocean where the radiative impact of the mineral

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

    NASA Astrophysics Data System (ADS)

    Penaloza-Murillo, Marcos A.

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

  1. Characteristics of regional aerosols: Southern Arizona and eastern Pacific Ocean

    NASA Astrophysics Data System (ADS)

    Prabhakar, Gouri

    Atmospheric aerosols impact the quality of our life in many direct and indirect ways. Inhalation of aerosols can have harmful effects on human health. Aerosols also have climatic impacts by absorbing or scattering solar radiation, or more indirectly through their interactions with clouds. Despite a better understanding of several relevant aerosol properties and processes in the past years, they remain the largest uncertainty in the estimate of global radiative forcing. The uncertainties arise because although aerosols are ubiquitous in the Earth's atmosphere they are highly variable in space, time and their physicochemical properties. This makes in-situ measurements of aerosols vital in our effort towards reducing uncertainties in the estimate of global radiative forcing due to aerosols. This study is an effort to characterize atmospheric aerosols at a regional scale, in southern Arizona and eastern Pacific Ocean, based on ground and airborne observations of aerosols. Metals and metalloids in particles with aerodynamic diameter (Dp) smaller than 2.5 μm are found to be ubiquitous in southern Arizona. The major sources of the elements considered in the study are identified to be crustal dust, smelting/mining activities and fuel combustion. The spatial and temporal variability in the mass concentrations of these elements depend both on the source strength and meteorological conditions. Aircraft measurements of aerosol and cloud properties collected during various field campaigns over the eastern Pacific Ocean are used to study the sources of nitrate in stratocumulus cloud water and the relevant processes. The major sources of nitrate in cloud water in the region are emissions from ships and wildfires. Different pathways for nitrate to enter cloud water and the role of meteorology in these processes are examined. Observations of microphysical properties of ambient aerosols in ship plumes are examined. The study shows that there is an enhancement in the number

  2. Aerosol algorithm evaluation within aerosol-CCI

    NASA Astrophysics Data System (ADS)

    Kinne, Stefan; Schulz, Michael; Griesfeller, Jan

    Properties of aerosol retrievals from space are difficult. Even data from dedicated satellite sensors face contaminations which limit the accuracy of aerosol retrieval products. Issues are the identification of complete cloud-free scenes, the need to assume aerosol compositional features in an underdetermined solution space and the requirement to characterize the background at high accuracy. Usually the development of aerosol is a slow process, requiring continuous feedback from evaluations. To demonstrate maturity, these evaluations need to cover different regions and seasons and many different aerosol properties, because aerosol composition is quite diverse and highly variable in space and time, as atmospheric aerosol lifetimes are only a few days. Three years ago the ESA Climate Change Initiative started to support aerosol retrieval efforts in order to develop aerosol retrieval products for the climate community from underutilized ESA satellite sensors. The initial focus was on retrievals of AOD (a measure for the atmospheric column amount) and of Angstrom (a proxy for aerosol size) from the ATSR and MERIS sensors on ENVISAT. The goal was to offer retrieval products that are comparable or better in accuracy than commonly used NASA products of MODIS or MISR. Fortunately, accurate reference data of ground based sun-/sky-photometry networks exist. Thus, retrieval assessments could and were conducted independently by different evaluation groups. Here, results of these evaluations for the year 2008 are summarized. The capability of these newly developed retrievals is analyzed and quantified in scores. These scores allowed a ranking of competing efforts and also allow skill comparisons of these new retrievals against existing and commonly used retrievals.

  3. Light absorption by secondary organic aerosol from α-pinene: Effects of oxidants, seed aerosol acidity, and relative humidity

    SciTech Connect

    Song, Chen; Gyawali, Madhu; Zaveri, Rahul A.; Shilling, John E.; Arnott, W. Patrick

    2013-10-25

    It is well known that light absorption from dust and black carbon aerosols has a warming effect on climate while light scattering from sulfate, nitrate, and sea salt aerosols has a cooling effect. However, there are large uncertainties associated with light absorption and scattering by different types of organic aerosols, especially in the near-UV and UV spectral regions. In this paper, we present the results from a systematic laboratory study focused on measuring light absorption by secondary organic aerosols (SOAs) generated from dark α-pinene + O3 and α-pinene + NOx + O3 systems in the presence of neutral and acidic sulfate seed aerosols. Light absorption was monitored using photoacoustic spectrometers at four different wavelengths: 355, 405, 532, and 870 nm. Significant light absorption at 355 and 405 nm was observed for the SOA formed from α-pinene + O3 + NO3 system only in the presence of highly acidic sulfate seed aerosols under dry conditions. In contrast, no absorption was observed when the relative humidity was elevated to greater than 27% or in the presence of neutral sulfate seed aerosols. Organic nitrates in the SOA formed in the presence of neutral sulfate seed aerosols were found to be nonabsorbing, while the light-absorbing compounds are speculated to be aldol condensation oligomers with nitroxy organosulfate groups that are formed in highly acidic sulfate aerosols. Finally and overall, these results suggest that dark α-pinene + O3 and α-pinene + NOx + O3 systems do not form light-absorbing SOA under typical atmospheric conditions.

  4. Leaf absorbance and photosynthesis

    NASA Technical Reports Server (NTRS)

    Schurer, Kees

    1994-01-01

    The absorption spectrum of a leaf is often thought to contain some clues to the photosynthetic action spectrum of chlorophyll. Of course, absorption of photons is needed for photosynthesis, but the reverse, photosynthesis when there is absorption, is not necessarily true. As a check on the existence of absorption limits we measured spectra for a few different leaves. Two techniques for measuring absorption have been used, viz. the separate determination of the diffuse reflectance and the diffuse transmittance with the leaf at a port of an integrating sphere and the direct determination of the non-absorbed fraction with the leaf in the sphere. In a cross-check both methods yielded the same results for the absorption spectrum. The spectrum of a Fuchsia leaf, covering the short-wave region from 350 to 2500 nm, shows a high absorption in UV, blue and red, the well known dip in the green and a steep fall-off at 700 nm. Absorption drops to virtually zero in the near infrared, with subsequent absorptions, corresponding to the water absorption bands. In more detailed spectra, taken at 5 nm intervals with a 5 nm bandwidth, differences in chlorophyll content show in the different depths of the dip around 550 nm and in a small shift of the absorption edge at 700 nm. Spectra for Geranium (Pelargonium zonale) and Hibiscus (with a higher chlorophyll content) show that the upper limit for photosynthesis can not be much above 700 nm. No evidence, however, is to be seen of a lower limit for photosynthesis and, in fact, some experiments down to 300 nm still did not show a decrease of the absorption although it is well recognized that no photosynthesis results with 300 nm wavelengths.

  5. Aerosol optical depths and their contributing sources in Taiwan

    NASA Astrophysics Data System (ADS)

    Chan, K. L.; Chan, K. L.

    2017-01-01

    In this paper, we present a quantitative investigation of the contributions of different aerosols to the aerosol optical depths (AODs) in Taiwan using a global chemical transport model (GEOS-Chem) and remote sensing measurements. The study focus is on the period from June 2012 to October 2013. Five different types of aerosols are investigated: sea salt, dust, sulfate, organic carbon and black carbon. Three of these aerosols, namely sulfate, organic carbon and black carbon, have significant anthropogenic sources. Model simulation results were compared with both ground based sun photometer measurements and MODerate resolution Imaging Spectroradiometer (MODIS) satellite observations. The model data shows good agreement with satellite observations (R = 0.72) and moderate correlation with sun photometer measurements (R = 0.52). Simulation results show the anthropogenic aerosols contribute ∼65% to the total AOD in Taipei, while natural originated aerosols only show a minor impact (∼35%). Among all the aerosols, sulfate is the dominating species, contributing 62.4% to the annual average total AOD. Organic carbon and black carbons respectively contribute 7.3% and 1.5% to the annual averaged total AOD. The annual average contributions of sea salt and dust aerosols to the total AOD are 26.4% and 2.4%, respectively. A sensitivity study was performed to identify the contributions of anthropogenic aerosol sources in each region to the AODs in Taipei. North-East Asia was identified as the major contributing source region of anthropogenic aerosols to Taipei, accounting for more than 50% of total sulfate, 32% of total organic carbon and 51% of total black carbon aerosols. South-East Asia is the second largest contributing source region, contributing 35%, 24% and 34% of total sulfate, organic carbon and black carbon aerosols, respectively. The aerosols from continents other than Asia only show minor impacts to the aerosol load in Taipei. In addition, a case study of a biomass

  6. Investigation the optical and radiative properties of aerosol vertical profile of boundary layer by lidar and ground based measurements

    NASA Astrophysics Data System (ADS)

    Chen, W.; Chou, C.; Lin, P.; Wang, S.

    2011-12-01

    The planetary boundary layer is the air layer near the ground directly affected by diurnal heat, moisture, aerosol, and cloud transfer to or from the surface. In the daytime solar radiation heats the surface, initiating thermal instability or convection. Whereas, the scattering and absorption of aerosols or clouds might decrease the surface radiation or heat atmosphere which induce feedbacks such as the enhanced stratification and change in relative humidity in the boundary layer. This study is aimed to understand the possible radiative effect of aerosols basing on ground based aerosol measurements and lidar installed in National Taiwan University in Taipei. The optical and radiative properties of aerosols are dominated by aerosol composition, particle size, hygroscopicity property, and shape. In this study, aerosol instruments including integrating nephelometer, open air nephelometer, aethalometer are applied to investigate the relationship between aerosol hygroscopicity properties and aerosol types. The aerosol hygroscopicity properties are further applied to investigate the effect of relative humidity on aerosol vertical profiles measured by a dual-wavelength and depolarization lidar. The possible radiative effect of aerosols are approached by vertical atmospheric extinction profiles measured by lidar. Calculated atmospheric and aerosol heating effects was compared with vertical meteorological parameters measured by radiosonde. The result shows light-absorbing aerosol has the potential to affect the stability of planetary boundary layer.

  7. Aerosol black carbon quantification in the central Indo-Gangetic Plain: Seasonal heterogeneity and source apportionment

    NASA Astrophysics Data System (ADS)

    Vaishya, Aditya; Singh, Prayagraj; Rastogi, Shantanu; Babu, S. Suresh

    2017-03-01

    Two years of aerosol spectral light absorption measurements, using filter based technique, from the central Indo-Gangetic plain (IGP), Gorakhpur (26.75°N, 83.38°E, 85 m amsl), are analyzed to study their seasonal behavior and to quantify their magnitude in terms of absorbing aerosols loading and source speciation. Spectral absorption analysis reveals a four-fold enhancement in absorption in winter (W) and post-monsoon (PoM) seasons at UV wavelengths as compared to IR wavelengths on account of increased biomass burning aerosol contribution to total absorbing aerosol load. Aerosols from the biomass sources contribute 28% during W and PoM seasons as against 16% in pre-monsoon (PM) and monsoon (M) seasons to the total absorbing aerosol content. A Mode shift in the distribution of the Absorption Ångström exponent (α) from 1.3 to 1.6 from PM-M seasons to PoM-W seasons signifies change in source type of absorbing aerosols from fossil fuel to biomass burning and their relative source strength. Due to near stagnant wind conditions combined with shallow boundary layer height, where air masses travelling to the central IGP are confined to a smaller volume, in W and PoM seasons, local sources assume more prominence rather than long-range transport of aerosols. Long-term measurements of aerosols physicochemical and radiative properties from this measurement location will enhance our understanding of the complex aerosol system over the IGP and its climatic implications.

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

    EPA Science Inventory

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

  9. Atmospheric correction of ocean color imagery: use of the junge power-law aerosol size distribution with variable refractive index to handle aerosol absorption.

    PubMed

    Chomko, R M; Gordon, H R

    1998-08-20

    When strongly absorbing aerosols are present in the atmosphere, the usual two-step procedure of processing ocean color data-(1) atmospheric correction to provide the water-leaving reflectance (rho(w)), followed by (2) relating rho(w) to the water constituents-fails and simultaneous estimation of the ocean and aerosol optical properties is necessary. We explore the efficacy of using a simple model of the aerosol-a Junge power-law size distribution consisting of homogeneous spheres with arbitrary refractive index-in a nonlinear optimization procedure for estimating the relevant oceanic and atmospheric parameters for case 1 waters. Using simulated test data generated from more realistic aerosol size distributions (sums of log-normally distributed components with different compositions), we show that the ocean's pigment concentration (C) can be retrieved with good accuracy in the presence of weakly or strongly absorbing aerosols. However, because of significant differences in the scattering phase functions for the test and power-law distributions, large error is possible in the estimate of the aerosol optical thickness. The positive result for C suggests that the detailed shape of the aerosol-scattering phase function is not relevant to the atmospheric correction of ocean color sensors. The relevant parameters are the aerosol single-scattering albedo and the spectral variation of the aerosol optical depth. We argue that the assumption of aerosol sphericity should not restrict the validity of the algorithm and suggest an avenue for including colored aerosols, e.g., wind-blown dust, in the procedure. A significant advantage of the new approach is that realistic multicomponent aerosol models are not required for the retrieval of C.

  10. Absorbent product to absorb fluids. [for collection of human wastes

    NASA Technical Reports Server (NTRS)

    Dawn, F. S.; Correale, J. V. (Inventor)

    1982-01-01

    A multi-layer absorbent product for use in contact with the skin to absorb fluids is discussed. The product utilizes a water pervious facing layer for contacting the skin, overlayed by a first fibrous wicking layer, the wicking layer preferably being of the one-way variety in which fluid or liquid is moved away from the facing layer. The product further includes a first container section defined by inner and outer layer of a water pervious wicking material between which is disposed a first absorbent mass. A second container section defined by inner and outer layers between which is disposed a second absorbent mass and a liquid impermeable/gas permeable layer. Spacesuit applications are discussed.

  11. Phase transition behaviour of sodium oleate aerosol particles

    NASA Astrophysics Data System (ADS)

    Nájera, Juan J.

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

  12. Anthropogenic Aerosols in Asia, Radiative Forcing, and Climate Change

    NASA Astrophysics Data System (ADS)

    Ramaswamy, V.; Bollasina, M. A.; Ming, Y.; Ocko, I.; Persad, G.

    2014-12-01

    Aerosols arising as a result of human-induced emissions in Asia form a key 'driver' in causing pollution and in the forcing of anthropogenic climate change. The manner of the forced climate change is sensitive to the scattering and absorption properties of the aerosols and the aerosol-cloud microphysical interactions. Using the NOAA/ GFDL global climate models and observations from multiple platforms, we investigate the radiative perturbations due to the 20th Century sulfate and carbonaceous aerosol emissions and the resultant impacts on surface temperature, tropical precipitation, Indian monsoon, hemispheric circulation, and atmospheric and oceanic heat transports. The influence of the aerosol species has many contrasts with that due to the anthropogenic well-mixed greenhouse gas emissions e.g., the asymmetry in the hemispheric climate response, but is subject to larger uncertainties. The aerosol forcing expected in the future indicates a significant control on the 21st Century anthropogenic climate change in Asia.

  13. The influence of metallurgy on the formation of welding aerosols.

    PubMed

    Zimmer, Anthony T

    2002-10-01

    Recent research has indicated that insoluble ultrafine aerosols (ie., particles whose physical diameters are less than 100 nm) may cause adverse health effects due to their small size, and that toxicological response may be more appropriately represented by particle number or particle surface area. Unfortunately, current exposure criteria and the associated air-sampling techniques are primarily mass-based. Welding processes are high-temperature operations that generate substantial number concentrations of ultrafine aerosols. Welding aerosols are formed primarily through the nucleation of metal vapors followed by competing growth mechanisms such as coagulation and condensation. Experimental results and mathematical tools are presented to illustrate how welding metallurgy influences the chemical aspects and dynamic processes that initiate and evolve the resultant aerosol. This research suggests that a fundamental understanding of metallurgy and aerosol physics can be exploited to suppress the formation of undesirable chemical species as well as the amount of aerosol generated during a welding process.

  14. Introducing GMXe: A new global aerosol dynamics and thermodynamics model for climate and air quality studies

    NASA Astrophysics Data System (ADS)

    Pringle, K.; Metzger, S.; Tost, H.; Steil, B.; Lelieveld, J.

    2009-04-01

    The treatment of aerosols in global atmospheric models has advanced significantly in the past decade, but the global aerosol distribution is very complex and simplifications must be made in order to treat aerosols in global models. One common simplification is in the treatment of the partitioning of semi-volatile species (e.g. NH3, HNO3 and H2O) between the gas and the aerosol phases, which is often neglected in models or treated in a simplified manner. The treatment of partitioning is, however, important as it controls the aerosol composition (including the aerosol water concentration) as well as affecting the concentration of both aerosol and gas phase pollutants. This paper introduces the newly developed GMXe aerosol model, which has been developed to investigate gas / aerosol partitioning on a global scale. The model (implemented within the ECHAM5/MESSy Atmospheric Chemistry (EMAC) model) combines an extended version of an established aerosol microphysics model (the M7, Stier et al ACP 2005) with a thermodynamic equilibrium model (EQSAM3, Metzger et al ACP 2008). The resulting model is capable of calculating gas / aerosol partitioning with relatively little additional computational overhead. In this paper we give an overview of the modelling approach used and show various model inter-comparisons, including a detailed comparison of the results of the GMXe and M7 models. We show the effect of including additional aerosol components - such as nitrate aerosol - on the global aerosol distribution and on the behaviour of other aerosol species (e.g. sulphate). The water uptake behaviour of the aerosol is examined, a factor that is important for the aerosol lifetime and also for the aerosol radiative forcing. We examine our results in the context of future emissions scenarios and air quality standards.

  15. An introduction to absorbent dressings.

    PubMed

    Jones, Menna Lloyd

    2014-12-01

    Exudate bathes the wound bed with a serous fluid that contains essential components that promote wound healing. However, excess exudate is often seen as a challenge for clinicians. Absorbent dressings are often used to aid in the management of exudate, with the aim of providing a moist but unmacerated environment. With so many different types of absorbent dressings available today-alongside making a holistic assessment-it is essential that clinicians also have the knowledge and skill to select the most appropriate absorbent dressing for a given patient.

  16. Self-Regulating Shock Absorber

    NASA Technical Reports Server (NTRS)

    Wesselski, Clarence J.

    1995-01-01

    Mechanical shock absorber keeps frictional damping force within tolerable limit. Its damping force does not increase with coefficient of friction between energy-absorbing components; rather, frictional damping force varies only slightly. Relatively insensitive to manufacturing variations and environmental conditions altering friction. Does not exhibit high breakaway friction and consequent sharp increase followed by sharp decrease in damping force at beginning of stroking. Damping force in absorber does not vary appreciably with speed of stroking. In addition, not vulnerable to leakage of hydraulic fluid.

  17. Distinct impact of different types of aerosols on surface solar radiation in China

    NASA Astrophysics Data System (ADS)

    Yang, Xin; Zhao, Chuanfeng; Zhou, Lijing; Wang, Yang; Liu, Xiaohong

    2016-06-01

    Observations of surface direct solar radiation (DSR) and visibility, particulate matter with aerodynamic diameters less than 2.5 µm (PM2.5), together with the aerosol optical thickness (AOT) taken from Moderate-Resolution Imaging Spectroradiometer and Multiangle Imaging Spectroradiometer, were investigated to gain insight into the impact of aerosol pollution on surface solar radiation in China. The surface DSR decreased during 2004-2014 compared with 1993~2003 over eastern China, but no clear reduction was observed in remote regions with cleaner air. Significant correlations of visibility, PM2.5, and regionally averaged AOT with the surface DSR over eastern China indicate that aerosol pollution greatly affects the energy available at the surface. The net loss of surface solar radiation also reduces the surface ground temperature over eastern China. However, the slope of the linear variation of the radiation with respect to atmospheric visibility is distinctly different at different stations, implying that the main aerosol type varies regionally. The largest slope value occurs at Zhengzhou and indicates that the aerosol absorption in central China is the highest, and lower slope values suggest relatively weakly absorbing types of aerosols at other locations. The spatial distribution of the linear slopes agrees well with the geographical distribution of the absorbing aerosols derived from the Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observations and Ozone Monitoring Instrument over China. The regional correlation between a larger slope value and higher absorbance properties of aerosols indicates that the net effects of aerosols on the surface solar energy and corresponding climatic effects are dependent on both aerosol amount and optical properties.

  18. Aromatic Structure in Simulates Titan Aerosol

    NASA Technical Reports Server (NTRS)

    Trainer, Melissa G.; Loeffler, M. J.; Anderson, C. M.; Hudson, R. L.; Samuelson, R. E.; Moore, M. A.

    2011-01-01

    Observations of Titan by the Cassini Composite Infrared Spectrometer (CIRS) between 560 and 20 per centimeter (approximately 18 to 500 micrometers) have been used to infer the vertical variations of Titan's ice abundances, as well as those of the aerosol from the surface to an altitude of 300 km [1]. The aerosol has a broad emission feature centered approximately at 140 per centimeter (71 micrometers). As seen in Figure 1, this feature cannot be reproduced using currently available optical constants from laboratory-generated Titan aerosol analogs [2]. The far-IR is uniquely qualified for investigating low-energy vibrational motions within the lattice structures of COITIDlex aerosol. The feature observed by CIRS is broad, and does not likely arise from individual molecules, but rather is representative of the skeletal movements of macromolecules. Since Cassini's arrival at Titan, benzene (C6H6) has been detected in the atmosphere at ppm levels as well as ions that may be polycyclic aromatic hydrocarbons (PAHs) [3]. We speculate that the feature may be a blended composite that can be identified with low-energy vibrations of two-dimensional lattice structures of large molecules, such as PAHs or nitrogenated aromatics. Such structures do not dominate the composition of analog materials generated from CH4 and N2 irradiation. We are performing studies forming aerosol analog via UV irradiation of aromatic precursors - specifically C6H6 - to understand how the unique chemical architecture of the products will influence the observable aerosol characteristics. The optical and chemical properties of the aromatic analog will be compared to those formed from CH4/N2 mixtures, with a focus on the as-yet unidentified far-IR absorbance feature. Preliminary results indicate that the photochemically-formed aromatic aerosol has distinct chemical composition, and may incorporate nitrogen either into the ring structure or adjoined chemical groups. These compositional differences are

  19. Generation and Characterization of Indoor Fungal Aerosols for Inhalation Studies.

    PubMed

    Madsen, Anne Mette; Larsen, Søren T; Koponen, Ismo K; Kling, Kirsten I; Barooni, Afnan; Karottki, Dorina Gabriela; Tendal, Kira; Wolkoff, Peder

    2016-04-01

    In the indoor environment, people are exposed to several fungal species. Evident dampness is associated with increased respiratory symptoms. To examine the immune responses associated with fungal exposure, mice are often exposed to a single species grown on an agar medium. The aim of this study was to develop an inhalation exposure system to be able to examine responses in mice exposed to mixed fungal species aerosolized from fungus-infested building materials. Indoor airborne fungi were sampled and cultivated on gypsum boards. Aerosols were characterized and compared with aerosols in homes. Aerosols containing 10(7)CFU of fungi/m(3)air were generated repeatedly from fungus-infested gypsum boards in a mouse exposure chamber. Aerosols contained Aspergillus nidulans,Aspergillus niger, Aspergillus ustus, Aspergillus versicolor,Chaetomium globosum,Cladosporium herbarum,Penicillium brevicompactum,Penicillium camemberti,Penicillium chrysogenum,Penicillium commune,Penicillium glabrum,Penicillium olsonii,Penicillium rugulosum,Stachybotrys chartarum, and Wallemia sebi They were all among the most abundant airborne species identified in 28 homes. Nine species from gypsum boards and 11 species in the homes are associated with water damage. Most fungi were present as single spores, but chains and clusters of different species and fragments were also present. The variation in exposure level during the 60 min of aerosol generation was similar to the variation measured in homes. Through aerosolization of fungi from the indoor environment, cultured on gypsum boards, it was possible to generate realistic aerosols in terms of species composition, concentration, and particle sizes. The inhalation-exposure system can be used to study responses to indoor fungi associated with water damage and the importance of fungal species composition.

  20. Generation and Characterization of Indoor Fungal Aerosols for Inhalation Studies

    PubMed Central

    Larsen, Søren T.; Koponen, Ismo K.; Kling, Kirsten I.; Barooni, Afnan; Karottki, Dorina Gabriela; Tendal, Kira; Wolkoff, Peder

    2016-01-01

    In the indoor environment, people are exposed to several fungal species. Evident dampness is associated with increased respiratory symptoms. To examine the immune responses associated with fungal exposure, mice are often exposed to a single species grown on an agar medium. The aim of this study was to develop an inhalation exposure system to be able to examine responses in mice exposed to mixed fungal species aerosolized from fungus-infested building materials. Indoor airborne fungi were sampled and cultivated on gypsum boards. Aerosols were characterized and compared with aerosols in homes. Aerosols containing 107 CFU of fungi/m3 air were generated repeatedly from fungus-infested gypsum boards in a mouse exposure chamber. Aerosols contained Aspergillus nidulans, Aspergillus niger, Aspergillus ustus, Aspergillus versicolor, Chaetomium globosum, Cladosporium herbarum, Penicillium brevicompactum, Penicillium camemberti, Penicillium chrysogenum, Penicillium commune, Penicillium glabrum, Penicillium olsonii, Penicillium rugulosum, Stachybotrys chartarum, and Wallemia sebi. They were all among the most abundant airborne species identified in 28 homes. Nine species from gypsum boards and 11 species in the homes are associated with water damage. Most fungi were present as single spores, but chains and clusters of different species and fragments were also present. The variation in exposure level during the 60 min of aerosol generation was similar to the variation measured in homes. Through aerosolization of fungi from the indoor environment, cultured on gypsum boards, it was possible to generate realistic aerosols in terms of species composition, concentration, and particle sizes. The inhalation-exposure system can be used to study responses to indoor fungi associated with water damage and the importance of fungal species composition. PMID:26921421

  1. Effect of Hydrophobic Primary Organic Aerosols on Secondary Organic Aerosol Formation from Ozonolysis of α-Pinene

    SciTech Connect

    Song, Chen; Zaveri, Rahul A.; Alexander, M. Lizabeth; Thornton, Joel A.; Madronich, Sasha; Ortega, John V.; Zelenyuk, Alla; Yu, Xiao-Ying; Laskin, Alexander; Maughan, A. D.

    2007-10-16

    Semi-empirical secondary organic aerosol (SOA) models typically assume a well-mixed organic aerosol phase even in the presence of hydrophobic primary organic aerosols (POA). This assumption significantly enhances the modeled SOA yields as additional organic mass is made available to absorb greater amounts of oxidized secondary organic gases than otherwise. We investigate the applicability of this critical assumption by measuring SOA yields from ozonolysis of α-pinene (a major biogenic SOA precursor) in a smog chamber in the absence and in the presence of dioctyl phthalate (DOP) and lubricating oil seed aerosol. These particles serve as surrogates for urban hydrophobic POA. The results show that these POA did not enhance the SOA yields. If these results are found to apply to other biogenic SOA precursors, then the semi-empirical models used in many global models would predict significantly less biogenic SOA mass and display reduced sensitivity to anthropogenic POA emissions than previously thought.

  2. Aerosol climate time series from ESA Aerosol_cci (Invited)

    NASA Astrophysics Data System (ADS)

    Holzer-Popp, T.

    2013-12-01

    Within the ESA Climate Change Initiative (CCI) the Aerosol_cci project (mid 2010 - mid 2013, phase 2 proposed 2014-2016) has conducted intensive work to improve algorithms for the retrieval of aerosol information from European sensors AATSR (3 algorithms), PARASOL, MERIS (3 algorithms), synergetic AATSR/SCIAMACHY, OMI and GOMOS. Whereas OMI and GOMOS were used to derive absorbing aerosol index and stratospheric extinction profiles, respectively, Aerosol Optical Depth (AOD) and Angstrom coefficient were retrieved from the other sensors. Global datasets for 2008 were produced and validated versus independent ground-based data and other satellite data sets (MODIS, MISR). An additional 17-year dataset is currently generated using ATSR-2/AATSR data. During the three years of the project, intensive collaborative efforts were made to improve the retrieval algorithms focusing on the most critical modules. The team agreed on the use of a common definition for the aerosol optical properties. Cloud masking was evaluated, but a rigorous analysis with a pre-scribed cloud mask did not lead to improvement for all algorithms. Better results were obtained using a post-processing step in which sudden transitions, indicative of possible occurrence of cloud contamination, were removed. Surface parameterization, which is most critical for the nadir only algorithms (MERIS and synergetic AATSR / SCIAMACHY) was studied to a limited extent. The retrieval results for AOD, Ångström exponent (AE) and uncertainties were evaluated by comparison with data from AERONET (and a limited amount of MAN) sun photometer and with satellite data available from MODIS and MISR. Both level2 and level3 (gridded daily) datasets were validated. Several validation metrics were used (standard statistical quantities such as bias, rmse, Pearson correlation, linear regression, as well as scoring approaches to quantitatively evaluate the spatial and temporal correlations against AERONET), and in some cases

  3. Thermodynamic characterization of Mexico City aerosol during MILAGRO 2006

    NASA Astrophysics Data System (ADS)

    Fountoukis, C.; Nenes, A.; Sullivan, A.; Weber, R.; van Reken, T.; Fischer, M.; Matías, E.; Moya, M.; Farmer, D.; Cohen, R. C.

    2009-03-01

    Fast measurements of aerosol and gas-phase constituents coupled with the ISORROPIA-II thermodynamic equilibrium model are used to study the partitioning of semivolatile inorganic species and phase state of Mexico City aerosol sampled at the T1 site during the MILAGRO 2006 campaign. Overall, predicted semivolatile partitioning agrees well with measurements. PM2.5 is insensitive to changes in ammonia but is to acidic semivolatile species. For particle sizes up to 1μm diameter, semi-volatile partitioning requires 15-30 min to equilibrate; longer time is typically required during the night and early morning hours. Aerosol and gas-phase speciation always exhibits substantial temporal variability, so that aerosol composition measurements (bulk or size-resolved) obtained over large integration periods are not reflective of its true state. When the aerosol sulfate-to-nitrate molar ratio is less than unity, predictions improve substantially if the aerosol is assumed to follow the deliquescent phase diagram. Treating crustal species as "equivalent sodium" (rather than explicitly) in the thermodynamic equilibrium calculations introduces important biases in predicted aerosol water uptake, nitrate and ammonium; neglecting crustals further increases errors dramatically. This suggests that explicitly considering crustals in the thermodynamic calculations is required to accurately predict the partitioning and phase state of aerosols.

  4. Spontaneous emission and absorber theory

    NASA Astrophysics Data System (ADS)

    Pegg, David T.

    1997-01-01

    One of the long term interests of George Series was the construction of a theory of spontaneous emission which does not involve field quantisation. His approach was written in terms of atomic operators only and he drew a parallel with the Wheeler-Feynman absorber theory of radiation. By making a particular extra postulate, he was able to obtain the correct spontaneous emission rate and the Lamb shift reasonably simply and directly. An examination of his approach indicates that this postulate is physically reasonable and the need for it arises because quantisation in his theory occurs after the response of the absorber has been accounted for by means of the radiative reaction field. We review briefly an alternative absorber theory approach to spontaneous emission based on the direct action between the emitting atom and a quantised absorber, and outline some applications to more recent effects of interest in quantum optics.

  5. Guided tissue regeneration. Absorbable barriers.

    PubMed

    Wang, H L; MacNeil, R L

    1998-07-01

    Over the past 15 years, techniques aimed at regeneration of lost periodontal tissue have become widely used and accepted in clinical practice. Among these techniques are those which use the principles of guided tissue regeneration (GTR), wherein barriers (i.e., membranes) are used to control cell and tissue repopulation of the periodontal wound. A variety of non-absorbable and absorbable barriers have been developed and used for this purpose, with a trend in recent years toward increased use of absorbable GTR materials. This article describes the evolution of absorbable barrier materials and overview materials available for clinical use today. In addition, advantages and disadvantages of these materials are discussed, as well as possible new developments in barrier-based GTR therapy.

  6. Measurements of Nitric Acid and Aerosol Species Aboard the NASA DC-8 Aircraft During the SASS OZone and Nitrogen Oxide Experiment (SONEX)

    NASA Technical Reports Server (NTRS)

    Talbot, Robert W.; Dibb, Jack E.

    1999-01-01

    The SASS Ozone and Nitrogen Oxides Experiment (SONEX) over the north Atlantic during October/November 1997 offered an excellent opportunity to examine the budget of total reactive nitrogen (NO(y)) in the upper troposphere (8 - 12 km altitude). The median measured NO(y) mixing ratio was 425 parts per trillion by volume (pptv). Two different methods were used to measure HNO3: (1) the mist chamber technique and, (2) chemical ionization mass spectrometry. Two merged data sets using these HNO3 measurements were used to calculate NO(y) by summing the reactive nitrogen species (a combination of measured plus modeled results) and comparing the resultant values to measured NO(y) (gold catalytic reduction method). Both comparisons showed good agreement in the two quantities (slope greater than 0.9 and r(sup 2) greater than 0.9). Thus, the total reactive nitrogen budget in the upper troposphere over the North Atlantic can be explained in a general manner as a simple mixture of NO(x). (NO + NO2), HNO3, and PAN. Median values of NO(x)/NO(y) were approx. = 0.25, HNO3/NO(y) approx. = 0.35 and PAN/NO(y) approx. = 0.17. Particulate NO3 and alkyl nitrates together composed less than 10% of NO(y), while model estimated HNO4 averaged 12%.

  7. Measurements of Nitric Acid and Aerosol Species Aboard the NASA DC-8 Aircraft During the SASS Ozone and Nitrogen Oxide Experiment (SONEX)

    NASA Technical Reports Server (NTRS)

    Talbot, Robert W.; Dibb, Jack E.

    1999-01-01

    The SASS Ozone and Nitrogen Oxides Experiment (SONEX) over the North Atlantic during October/November 1997 offered an excellent opportunity to examine the budget of total reactive nitrogen (NO(sub y)) in the upper troposphere (8 - 12 km altitude). The median measured NO(sub y) mixing ratio was 425 parts per trillion by volume (pptv). Two different methods were used to measure HNO3: (1) the mist chamber technique and, (2) chemical ionization mass spectrometry. Two merged data sets using these HNO3 measurements were used to calculate NO(sub y) by summing the reactive nitrogen species (a combination of measured plus modeled results) and comparing the resultant values to measured NO(sub y) (gold catalytic reduction method). Both comparisons showed good agreement in the two quantities (slope > 0.9 and r(exp 2) > 0.9). Thus, the total reactive nitrogen budget in the upper troposphere over the North Atlantic can be explained in a general manner as a simple mixture of NO(sub x). (NO + NO2), HNO3, and PAN. Median values of NO(sub x)/NO(sub y) were approximately equal to 0.25, HNO3/NO(sub y) were approximately equal to 0.35 and Peroxyacetyl Nitrate (PAN)/NO(sub y) were approximately equal to 0. 17. Particulate NO3 and alkyl nitrates together composed <10 % of NO(sub y), while model estimated HNO4 averaged 12%.

  8. Profiling Transboundary Aerosols over Taiwan and Assessing Their Radiative Effects

    NASA Technical Reports Server (NTRS)

    Wang, Sheng-Hsiang; Lin, Neng-Huei; Chou, Ming-Dah; Tsay, Si-Chee; Welton, Ellsworth J.; Hsu, N. Christina; Giles, David M.; Liu, Gin-Rong; Holben, Brent N.

    2010-01-01

    A synergistic process was developed to study the vertical distributions of aerosol optical properties and their effects on solar heating using data retrieved from ground-based radiation measurements and radiative transfer simulations. Continuous MPLNET and AERONET observations were made at a rural site in northern Taiwan from 2005 to 2007. The aerosol vertical extinction profiles retrieved from ground-based lidar measurements were categorized into near-surface, mixed, and two-layer transport types, representing 76% of all cases. Fine-mode (Angstrom exponent, alpha, approx.1.4) and moderate-absorbing aerosols (columnar single-scattering albedo approx.0.93, asymmetry factor approx.0.73 at 440 nm wavelength) dominated in this region. The column-integrated aerosol optical thickness at 500 nm (tau(sub 500nm)) ranges from 0.1 to 0.6 for the near-surface transport type, but can be doubled in the presence of upper-layer aerosol transport. We utilize aerosol radiative efficiency (ARE; the impact on solar radiation per unit change of tau(sub 500nm)) to quantify the radiative effects due to different vertical distributions of aerosols. Our results show that the ARE at the top-of-atmosphere (-23 W/ sq m) is weakly sensitive to aerosol vertical distributions confined in the lower troposphere. On the other hand, values of the ARE at the surface are -44.3, -40.6 and -39.7 W/sq m 38 for near-surface, mixed, and two-layer transport types, respectively. Further analyses show that the impact of aerosols on the vertical profile of solar heating is larger for the near-surface transport type than that of two-layer transport type. The impacts of aerosol on the surface radiation and the solar heating profiles have implications for the stability and convection in the lower troposphere.

  9. Global and Seasonal Aerosol Optical Depths Derived From Ultraviolet Observations by Satellites (TOMS)

    NASA Technical Reports Server (NTRS)

    Herman, J. R.; Torres, O.

    1999-01-01

    It has been shown that absorbing aerosols (dust, smoke, volcanic ash) can be detected in the ultraviolet wavelengths (331 nm to 380 nm) from satellite observations (TOMS, Total Ozone Mapping Spectrometer) over both land and water. The theoretical basis for these observations and their conversions to optical depths is discussed in terms of an aerosol index AI or N-value residue (assigned positive for absorbing aerosols). The theoretical considerations show that negative values of the AI frequently represent the presence of non-absorbing aerosols (NA) in the troposphere (mostly pollution in the form of sulfates, hydrocarbons, etc., and some natural sulfate aerosols) with particle sizes near 0.1 to 0.2 microns or less. The detection of small-particle non-absorbing aerosols from the measured backscattered radiances is based on the observed wavelength dependence from Mie scattering after the background Rayleigh scattering is subtracted. The Mie scattering from larger particles, 1 micron or more (e.g., cloud water droplets) has too small a wavelength dependence to be detected by this method. In regions that are mostly cloud free, aerosols of all sizes can be seen in the single channel 380 nm or 360 nm radiance data. The most prominent Al feature observed is the strong asymmetry in aerosol amount between the Northern and Southern Hemispheres, with the large majority of NA occurring above 20degN latitude. The maximum values of non-absorbing aerosols are observed over the eastern U.S. and most of western Europe corresponding to the areas of highest industrial pollution. Annual cycles in the amount of NA are observed over Europe and North America with maxima occurring in the summer corresponding to times of minimum wind transport. Similarly, the maxima in the winter over the Atlantic Ocean occurs because of wind borne transport from the land. Most regions of the world have the maximum amount of non-absorbing aerosol in the December to January period except for the eastern

  10. Countercurrent flow absorber and desorber

    DOEpatents

    Wilkinson, W.H.

    1984-10-16

    Countercurrent flow absorber and desorber devices are provided for use in absorption cycle refrigeration systems and thermal boosting systems. The devices have increased residence time and surface area resulting in improved heat and mass transfer characteristics. The apparatuses may be incorporated into open cycle thermal boosting systems in which steam serves both as the refrigerant vapor which is supplied to the absorber section and as the supply of heat to drive the desorber section of the system. 9 figs.

  11. Countercurrent flow absorber and desorber

    DOEpatents

    Wilkinson, William H.

    1984-01-01

    Countercurrent flow absorber and desorber devices are provided for use in absorption cycle refrigeration systems and thermal boosting systems. The devices have increased residence time and surface area resulting in improved heat and mass transfer characteristics. The apparatuses may be incorporated into open cycle thermal boosting systems in which steam serves both as the refrigerant vapor which is supplied to the absorber section and as the supply of heat to drive the desorber section of the system.

  12. Operational aerosol and dust storm forecasting

    NASA Astrophysics Data System (ADS)

    Westphal, D. L.; Curtis, C. A.; Liu, M.; Walker, A. L.

    2009-03-01

    The U. S. Navy now conducts operational forecasting of aerosols and dust storms on global and regional scales. The Navy Aerosol Analysis and Prediction System (NAAPS) is run four times per day and produces 6-day forecasts of sulfate, smoke, dust and sea salt aerosol concentrations and visibility for the entire globe. The Coupled Ocean Atmosphere Mesoscale Prediction System (COAMPS®) is run twice daily for Southwest Asia and produces 3-day forecasts of dust, smoke, and visibility. The graphical output from these models is available on the Internet (www.nrlmry.navy.mil/aerosol/). The aerosol optical properties are calculated for each specie for each forecast output time and used for sea surface temperature (SST) retrieval corrections, regional electro-optical (EO) propagation assessments, and the development of satellite algorithms. NAAPS daily aerosol optical depth (AOD) values are compared with the Advanced Very High Resolution Radiometer (AVHRR) and Moderate Resolution Imaging Spectroradiometer (MODIS) AOD values. Visibility forecasts are compared quantitatively with surface synoptic reports.

  13. Regional transport of anthropogenic pollution and dust aerosols in spring to Tianjin - A coastal megacity in China.

    PubMed

    Su, Xiaoli; Wang, Qiao; Li, Zhengqiang; Calvello, Mariarosaria; Esposito, Francesco; Pavese, Giulia; Lin, Meijing; Cao, Junji; Zhou, Chunyan; Li, Donghui; Xu, Hua

    2017-04-15

    Simultaneous measurements of columnar aerosol microphysical and optical properties, as well as PM2.5 chemical compositions, were made during two types of spring pollution episodes in Tianjin, a coastal megacity of China. The events were investigated using field observations, satellite data, model simulations, and meteorological fields. The lower Ångström Exponent and the higher aerosol optical depth on 29 March, compared with the earlier event on 26 March, implied a dominance of coarse mode particles - this was consistent with the differences in volume-size distributions. Based on the single scattering spectra, the dominant absorber (at blue wavelength) changed from black carbon during less polluted days to brown carbon on 26 March and dust on 29 March. The concentrations of major PM2.5 species for these two episodes also differed, with the earlier event enriched in pollution-derived substances and the later with mineral dust elements. The formation mechanisms of these two pollution episodes were also examined. The 26 March episode was attributed to the accumulation of both local emissions and anthropogenic pollutants transported from the southwest of Tianjin under the control of high pressure system. While the high aerosol loading on 29 March was caused by the mixing of transported dust from northwest source region with local urban pollution. The mixing of transported anthropogenic pollutants and dust with local emissions demonstrated the complexity of springtime pollution in Tianjin. The synergy of multi-scale observations showed excellent potential for air pollution study.

  14. Tropospheric Trace Gas Interactions with Aerosols

    NASA Technical Reports Server (NTRS)

    Penner, Joyce E.; Maddrea, George L., Jr. (Technical Monitor)

    2002-01-01

    Tropospheric aerosols are of considerable environmental importance. They modify the radiative budget of Earth by scattering and absorbing radiation, and by providing nuclei for cloud formation. Additionally, they provide surfaces for heterogeneous and multiphase reactions that affect tropospheric chemistry. For example, Dentener and Crutzen (1993) showed that reactions of N2O5 and NO3 with sulfate aerosols may significantly alter the tropospheric concentrations of NO(x), O3, and OH by converting NOx to HNO3 which is rapidly removed by precipitation. Zhang et al. (1994) assumed these same reactions would occur on dust aerosols and showed that dust outbreaks may reduce NO(x) levels by up to 50%. Dentener et al. (1996) studied the possible effect of reactions on dust on sulfate, nitrate, and O3 concentration. Heterogeneous and multiphase reactions on aerosols may also perturb the sulfur cycle the chlorine cycle and the bromine cycle. Because these reactions can release free chlorine and free bromine they might lead to the destruction of ozone in the marine boundary layer that may be important to include in models of tropospheric chemistry. The goal of our proposed work is to examine the role of heterogeneous and multiphase reactions in the tropospheric cycles of reactive nitrogen and sulfur.

  15. Reducing the Uncertainties in Direct Aerosol Radiative Forcing

    NASA Technical Reports Server (NTRS)

    Kahn, Ralph A.

    2011-01-01

    Airborne particles, which include desert and soil dust, wildfire smoke, sea salt, volcanic ash, black carbon, natural and anthropogenic sulfate, nitrate, and organic aerosol, affect Earth's climate, in part by reflecting and absorbing sunlight. This paper reviews current status, and evaluates future prospects for reducing the uncertainty aerosols contribute to the energy budget of Earth, which at present represents a leading factor limiting the quality of climate predictions. Information from satellites is critical for this work, because they provide frequent, global coverage of the diverse and variable atmospheric aerosol load. Both aerosol amount and type must be determined. Satellites are very close to measuring aerosol amount at the level-of-accuracy needed, but aerosol type, especially how bright the airborne particles are, cannot be constrained adequately by current techniques. However, satellite instruments can map out aerosol air mass type, which is a qualitative classification rather than a quantitative measurement, and targeted suborbital measurements can provide the required particle property detail. So combining satellite and suborbital measurements, and then using this combination to constrain climate models, will produce a major advance in climate prediction.

  16. Perfect selective metamaterial solar absorbers.

    PubMed

    Wang, Hao; Wang, Liping

    2013-11-04

    In this work, we numerically investigate the radiative properties of metamaterial nanostructures made of two-dimensional tungsten gratings on a thin dielectric spacer and an opaque tungsten film from UV to mid-infrared region as potential selective solar absorbers. The metamaterial absorber with single-sized tungsten patches exhibits high absorptance in the visible and near-infrared region due to several mechanisms such as surface plasmon polaritons, magnetic polaritons, and intrinsic bandgap absorption of tungsten. Geometric effects on the resonance wavelengths and the absorptance spectra are studied, and the physical mechanisms are elucidated in detail. The absorptance could be further enhanced in a broader spectral range with double-sized metamaterial absorbers. The total solar absorptance of the optimized metamaterial absorbers at normal incidence could be more than 88%, while the total emittance is less than 3% at 100°C, resulting in total photon-to-heat conversion efficiency of 86% without any optical concentration. Moreover, the metamaterial solar absorbers exhibit quasi-diffuse behaviors as well as polarization independence. The results here will facilitate the design of novel highly efficient solar absorbers to enhance the performance of various solar energy conversion systems.

  17. Light absorbing carbon emissions from commercial shipping

    NASA Astrophysics Data System (ADS)

    Lack, Daniel; Lerner, Brian; Granier, Claire; Baynard, Tahllee; Lovejoy, Edward; Massoli, Paola; Ravishankara, A. R.; Williams, Eric

    2008-07-01

    Extensive measurements of the emission of light absorbing carbon aerosol (LAC) from commercial shipping are presented. Vessel emissions were sampled using a photoacoustic spectrometer in the Gulf of Mexico region. The highest emitters (per unit fuel burnt) are tug boats, thus making significant contributions to local air quality in ports. Emission of LAC from cargo and non cargo vessels in this study appears to be independent of engine load. Shipping fuel consumption data (2001) was used to calculate a global LAC contribution of 133(+/-27) Ggyr-1, or ~1.7% of global LAC. This small fraction could have disproportionate effects on both air quality near port areas and climate in the Arctic if direct emissions of LAC occur in that region due to opening Arctic sea routes. The global contribution of this LAC burden was investigated using the MOZART model. Increases of 20-50 ng m-3 LAC (relative increases up to 40%) due to shipping occur in the tropical Atlantic, Indonesia, central America and the southern regions of South America and Africa.

  18. Climate effects of anthropogenic aerosols over East Asia based on modeling study

    NASA Astrophysics Data System (ADS)

    Mukai, Makiko

    The increasing emission of anthropogenic aerosols causes serious air pollution episodes and various effects on the climate by the aerosols interacting with the radiation budget by directly absorbing and scattering the solar radiation, and by them indirectly modifying the optical properties and lifetimes of clouds. In East Asia anthropogenic aerosol concentrations are rapidly increasing. It is therefore necessary to evaluate the sensitivity of anthropogenic aerosols upon the radiative forcing in this region. For this purpose we utilize an atmospheric general circulation model (AGCM) with an aerosol transport and radiation model and an ocean mixed-layer model. The model in this study was a three-dimensional aerosol transport-radiation model (SPRINTARS), driven by the AGCM developed by CCSR (Center for Climate System Research), NIES (National Institute for Environmental Studies), and FRCGC (Frontier Research Center for Global Change). This model incorporates sulfate, carbonaceous, sea salt, and mineral dust aerosols, the first three of which are assumed to acts as cloud condensation nuclei that generate cloud droplets whose number increases with the number of nuclei. We assumed sulfate and carbonaceous aerosol from fuel burning for anthropogenic aerosol. And the model simulations of equilibrium experiments were performed to investigate the impact of anthropogenic aerosols based on present-day emission data and the preindustrial-era emission data. Our simulation results showed that copious anthropogenic aerosol loading causes significant decrease in the surface downward shortwave radiation flux (SDSWRF), which indicates that a direct effect of aerosols has the greatest influence on the surface radiation. It is found from our model simulations that low-level clouds increase but convective clouds decrease due to reduced convective activity caused by surface cooling when anthropogenic aerosol increases. It was also found that the contributions of aerosols to the radiation

  19. Overview of Aerosol Distribution

    NASA Technical Reports Server (NTRS)

    Kaufman, Yoram

    2005-01-01

    Our knowledge of atmospheric aerosols (smoke, pollution, dust or sea salt particles, small enough to be suspended in the air), their evolution, composition, variability in space and time and interaction with clouds and precipitation is still lacking despite decades of research. Understanding the global aerosol system is fundamental for progress in climate change and hydrological cycle research. While a single instrument was used to demonstrate 50 years ago that the global CO2 levels are rising, posing threat of global warming, we need an array of satellites and field measurements coupled with chemical transport models to understand the global aerosol system. This complexity of the aerosol problem results from their short lifetime (1 week) and variable chemical composition. A new generation of satellites provides exciting opportunities to measure the global distribution of aerosols, distinguishing natural from anthropogenic aerosol and measuring their interaction with clouds and climate. I shall discuss these topics and application of the data to air quality monitoring.

  20. X-Ray Microspectroscopic Investigations of Remote Aerosol Composition and Changes in Aerosol Microstructure and Phase State upon Hydration

    NASA Astrophysics Data System (ADS)

    Andreae, M. O.; Artaxo, P.; Bechtel, M.; Förster, J. D.; Kilcoyne, A. L. D.; Krüger, M. L.; Pöhlker, C.; Saturno, J.; Weigand, M.; Wiedemann, K. T.

    2014-12-01

    Atmospheric aerosols play a crucial role in the Earth's climate system and hydrological cycle by scattering and absorbing sunlight and affecting the formation and development of clouds and precipitation. Our research focuses on aerosols in remote regions, in order to characterize the properties and sources of natural aerosol particles and the extent of human perturbations of the aerosol burden. The phase and mixing state of atmospheric aerosols, and particularly their hygroscopic response to relative humidity (RH) v