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Sample records for aerosol number concentrations

  1. Intercomparison of aerosol instruments: number concentration

    SciTech Connect

    Knutson, E O; Sinclair, D; Tu, K W; Hinchliffe, L; Franklin, H

    1982-05-01

    An intercomparison of aerosol instruments conducted February 23-27, 1981, at the Environmental Measurements Laboratory (EML) focused on five instruments: the Pollak and TSI condensation nucleus counters; the Active Scattering Aerosol Spectrometer (ASAS-X); and two aerosol electrometers. Test aerosols of sodium chloride and ammonium fluorescein generated by nebulization/electrostatic classification were used to obtain 195 lines of comparison data. Concentrations measured by the ASAS-X and the TSI aerosol electrometer averaged respectively 1.388 and 1.581 times that measured by the Pollak. These ratios were very stable during the week and there was little effect of particle size or material. Most other comparisons were equally stable. However, a review of past work at EML and elsewhere led to the disturbing conclusion that these ratios may change from year to year, or from season to season. A filter sample was taken from microscopy, concurrent with readings from the ASAS-X and the TSI condensation nucleus counters. In this sample, the two instruments differed by 20%. Within its 20% uncertainty, the filter result matched both the TSI and ASAS-X readings.

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

    NASA Astrophysics Data System (ADS)

    Lee, Y. H.; Adams, P. J.; Shindell, D. T.

    2014-09-01

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

  3. Effect of aerosol number concentration on cloud droplet dispersion: An LES study and implications for aerosol indirect forcing

    NASA Astrophysics Data System (ADS)

    Lu, M.; Seinfeld, J. H.

    2005-12-01

    Through three-dimensional LES simulations of marine stratocumulus we explore the factors that control the cloud spectral relative dispersion (ratio of cloud droplet spectral width to the mean radius of the distribution) as a function of aerosol number concentration and the extent to which the relative dispersion either enhances or mitigates the Twomey effect. We find that relative dispersion decreases with increasing aerosol number concentration (for aerosol number concentrations less than about 1000 cm- 3) because smaller droplets resulting from higher aerosol number concentrations inhibit precipitation and lead to: (1) less spectral broadening by suppressed collision and coalescence processes; and (2) more spectral narrowing by droplet condensational growth at higher updraft velocity, because reduced drizzle latent heating at cloud top results in increased boundary layer turbulent kinetic energy production by buoyancy and thereby stronger turbulence. Increased spectral broadening owing to increased cloud-top entrainment mixing, also as a result of increased boundary layer turbulence, is relatively insignificant compared with (1) and (2). The coefficient k, an important parameter that relates cloud droplet effective radius and volume mean radius in large-scale models, is a function of skewness and relative dispersion of the distribution and is negatively correlated with relative dispersion. Increasing k with increasing aerosol number concentration leads to maximum enhancement of the cloud susceptibility (the change of cloud optical depth due to change of cloud droplet number concentration) over that attributable to the Twomey effect alone by about 4.2% and 39% for simulated FIRE and ASTEX cases, respectively.

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

    NASA Astrophysics Data System (ADS)

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

    2013-06-01

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

  5. On the contribution of organics to the North East Atlantic aerosol number concentration

    NASA Astrophysics Data System (ADS)

    Bialek, Jakub; Dall'Osto, Manuel; Monahan, Ciaran; Beddows, David; O'Dowd, Colin

    2012-12-01

    k-means statistical-cluster analysis of submicron aerosol size distributions is combined with coincident humidity tandem differential mobility analyser data, leading to five unique aerosol categories for hygroscopic growth factors (HGFs): low sea-salt background marine, high sea-salt background marine, coastal nucleation, open ocean nucleation and anthropogenically influenced scenarios. When considering only marine conditions, and generic aerosol species associated with this environment (e.g. non-sea-salt sulfate, sea-salt, partly soluble organic matter and water insoluble organic matter), the two-year annual average contribution to aerosol number concentration from the different generic species was made up as follows: 46% (30-54%) of partially modified ammonium sulfate particles; 23% (11-40%) of partially modified sea-salt; and the remaining 31% (25-35%) contribution attributed to two distinct organic species as evidenced by different, but low, HGFs. The analysis reveals that on annual timescales, ˜30% of the submicron marine aerosol number concentration is sourced from predominantly organic aerosol while 60% of the anthropogenic aerosol number is predominantly organic. Coastal nucleation events show the highest contribution of the lowest HGF mode (1.19), although this contribution is more likely to be influenced by inorganic iodine oxides. While organic mass internally mixed with inorganic salts will lower the activation potential of these mixed aerosol types, thereby potentially reducing the concentration of cloud condensation nuclei (CCN), pure organic water soluble particles are still likely to be activated into cloud droplets, thereby increasing the concentration of CCN. A combination of dynamics and aerosol concentrations will determine which effect will prevail under given conditions.

  6. Influence of the external mixing state of atmospheric aerosol on derived CCN number concentrations

    NASA Astrophysics Data System (ADS)

    Wex, H.; McFiggans, G.; Henning, S.; Stratmann, F.

    2010-05-01

    We derived the range of particle hygroscopicities ($\\kappa$) that occurs in the atmosphere, based on literature data of measured hygroscopic growth or based on chemical composition. The derived $\\kappa$-values show that the atmospheric aerosol often is an external mixture with respect to hygroscopicity. Mean $\\kappa$ were derived for urban, rural, and marine aerosols for the different hygroscopic modes. Using these $\\kappa$ and exemplary particle number size distributions for the different aerosols, the number concentration of cloud condensation nuclei (NCCN) was derived for two cases, (1) accounting for the less hygroscopic fraction of particles and (2) assuming all particles to have $\\kappa$ of the more hygroscopic mode. NCCN derived from measured particle hygroscopicity is overestimated for case (2). Overestimation of NCCN is largest for fresh continental aerosol and less pronounced for marine aerosol. With $\\kappa$ derived from bulk aerosol composition data, only the hygroscopicity of more soluble aerosol particles is captured. Bulk or even size-resolved composition data will be insufficient to predict NCCN under many conditions unless independent information about particle mixing state is available.

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

    SciTech Connect

    Meskhidze, Nicholas

    2013-10-21

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

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

    NASA Astrophysics Data System (ADS)

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

    2016-04-01

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

  9. On the submicron aerosol distributions and CCN number concentrations in and around the Korean Peninsula

    NASA Astrophysics Data System (ADS)

    Kim, J. H.; Yum, S. S.; Shim, S.; Kim, W. J.; Park, M.; Kim, J.-H.; Kim, M.-H.; Yoon, S.-C.

    2014-08-01

    Total number concentrations of particles having a diameter larger than 10 nm (NCN), cloud condensation nuclei at several supersaturation (S) values (NCCN) and number size distributions of particles with 10-414 nm diameter were measured in Seoul between 2004 and 2010. Overall average values of NCN and geometric mean diameter were 17 811 ± 5581 cm-3 and 48 ± 6 nm. Average NCCN at 0.4, 0.6 and 0.8% S were 4145 ± 2016, 5323 ± 2453 and 6067 ± 2780 cm-3 and corresponding NCCN / NCN were 0.26 ± 0.11, 0.33 ± 0.11 and 0.37 ± 0.12. There is a clear seasonal variation in aerosol concentration, which seems to be due to the monsoon. NCN and NCCN are also found to depend on the volume of traffic and the height of the planetary boundary layer, respectively. During aircraft campaigns in 2009 and 2011, NCN and NCCN at 0.6% S (N0.6%) were measured in and around the Korean Peninsula. During the 2011 campaign, the aerosol scattering coefficient was also measured. NCN and N0.6% in the lower altitudes were generally higher than at higher altitudes, except for cases when particle formation and growth events were thought to occur at higher altitudes. NCN and N0.6% generally show a positive correlation with aerosol scattering coefficients but this correspondence tends to vary with altitude. Occasional instances of low (< 0.3) N0.6% / NCN in the boundary layer are demonstrated to be associated with particle formation and growth events. With the support of ground measurements, it is confirmed that a particle formation and growth event did indeed occur over the Yellow Sea on a flight day, and the areal extent of this event is estimated to be greater than 100 km × 450 km. With the combination of the current and several relevant previous studies, a composite map of NCN and NCCN in and around the Korean Peninsula is produced. Overall, the exhibited concentrations are typical of values measured over polluted regions elsewhere on the globe. Moreover, there is a generally decreasing trend

  10. On the submicron aerosol distributions and CCN number concentrations in and around the Korean Peninsula

    NASA Astrophysics Data System (ADS)

    Kim, J. H.; Yum, S. S.; Shim, S.; Kim, W. J.; Park, M.; Kim, J.; Kim, M.; Yoon, S. C.

    2014-03-01

    Total number concentrations of particles having diameter larger than 10 nm (NCN), cloud condensation nuclei at several supersaturation (S) values (NCCN), and the number size distribution of particles for 10-414 nm particle diameter range were measured in Seoul between 2004 and 2010. Overall average values of NCN and geometric mean diameter are 17 811 ± 5581 cm-3 and 48 ± 6 nm, respectively. Average NCCN at 0.4, 0.6, and 0.8% S are 4145 ± 2016, 5323 ± 2453 and 6067 ± 2780 cm-3, respectively and corresponding NCCN / NCN are 0.26 ± 0.11, 0.33 ± 0.11 and 0.37 ± 0.12. There is a clear seasonal variation of aerosol concentration, which seems to be due to the monsoon. NCN and NCCN are also found to be dependent on the volume of traffic and the height of planetary boundary layer, respectively. During the two aircraft campaigns in 2009 and 2011, NCN and NCCN at 0.6% S were measured in and around the Korean Peninsula. During the 2011 campaign, aerosol scattering coefficient was also measured. NCN and NCCN 0.6 in the lower altitudes were generally higher than at higher altitudes, except for the cases when particle formation and growth events are thought to occur at higher altitudes. NCN and NCCN 0.6 show generally a positive correlation with aerosol scattering coefficients but its correspondence tends to vary with altitude. Occasional instances of low (< 0.3) NCCN 0.6 / NCN in the boundary layer are demonstrated to be associated with particle formation and growth events. With the support of ground measurements, it is confirmed that a particle formation and growth event indeed occurred on a flight day over the Yellow Sea and the areal extent of the event is estimated to be greater than 100 km × 450 km. With the combination of the current and several relevant previous studies, a composite map of NCN and NCCN in and around the Korean Peninsula is produced. Overall, the exhibited concentrations are typical of the values measured over the polluted regions elsewhere in the

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

    NASA Astrophysics Data System (ADS)

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

    2009-04-01

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

  12. Effect of aerosol number concentration on cloud droplet dispersion: A large-eddy simulation study and implications for aerosol indirect forcing

    NASA Astrophysics Data System (ADS)

    Lu, Miao-Ling; Seinfeld, John H.

    2006-01-01

    Through three-dimensional large-eddy simulations of marine stratocumulus we explore the factors that control the cloud spectral relative dispersion (ratio of cloud droplet spectral width to the mean radius of the distribution) as a function of aerosol number concentration and the extent to which the relative dispersion either enhances or mitigates the Twomey effect. We find that relative dispersion decreases with increasing aerosol number concentration (for aerosol number concentrations less than about 1000 cm-3) because smaller droplets resulting from higher aerosol number concentrations inhibit precipitation and lead to (1) less spectral broadening by suppressed collision and coalescence processes and (2) more spectral narrowing by droplet condensational growth at higher updraft velocity because reduced drizzle latent heating at cloud top results in increased boundary layer turbulent kinetic energy production by buoyancy and thereby stronger turbulence. Increased spectral broadening owing to increased cloud-top entrainment mixing, also as a result of increased boundary layer turbulence, is relatively insignificant compared with outcomes 1 and 2. The coefficient k, an important parameter that relates cloud droplet effective radius and volume mean radius in large-scale models, is a function of skewness and relative dispersion of the distribution and is negatively correlated with relative dispersion. Increasing k with increasing aerosol number concentration leads to maximum enhancement of the cloud susceptibility (the change of cloud optical depth due to change of cloud droplet number concentration) over that attributable to the Twomey effect alone by about 4.2% and 39% for simulated FIRE and ASTEX cases, respectively.

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

    NASA Astrophysics Data System (ADS)

    Logan, Timothy S.

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

  14. Relationship and variations of aerosol number and PM 10 mass concentrations in a highly polluted urban environment—New Delhi, India

    NASA Astrophysics Data System (ADS)

    Mönkkönen, P.; Uma, R.; Srinivasan, D.; Koponen, I. K.; Lehtinen, K. E. J.; Hämeri, K.; Suresh, R.; Sharma, V. P.; Kulmala, M.

    Measurements of the aerosol number concentration and the PM 10 mass concentrations of urban background aerosols in different seasons were performed in New Delhi 2002, including the simultaneous measurements of NO 2, SO 2 and CO concentrations. The results indicate an interesting relationship between the aerosol number and the PM 10 mass concentrations. The number concentration increases with the mass concentration up to 300 μg m -3. However, after this point, the number concentration decreases even if the mass concentration increases. An explanation for this nonlinear behavior is proposed through a dynamic model involving the coagulation sink concept. The linear relationship between the mass and the number concentration in ambient air is valid if the mass concentration is relatively low. A high sink, however, means that the number concentration cannot be high—resulting in a decline in the number vs. mass plot. Clear diurnal, weekly and seasonal variations in concentrations were observed. High number concentrations of aerosols were observed in the mornings (7-8 a.m.) and in the evenings (7-10 p.m.). The number concentration was highest in March and lowest in June and the mass concentration was highest in November and lowest in June. The number concentration was higher during weekdays, but the mass concentration was higher during weekends. The number concentration correlates with the NO 2 concentration, which indicates that one major source of aerosol particles for the monitored site in New Delhi may be vehicular emission, but also domestic use of fossil fuels and biofuels cannot be neglected.

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

    NASA Technical Reports Server (NTRS)

    Meskhidze, Nicholas; Petters, Markus; Tsigaridis, Kostas; Bates. Tim; O'Dowd, Colin; Reid, Jeff; Lewis, Ernie R.; Gantt, Brett; Anguelova, Magdalena D.; Bhave, Prakash V.; Bird, James; Callaghan, Adrian H.; Ceburnis, Darius; Chang, Rachel; Clark, Antony; deLeeuw, Gerrit; Deane, Grant; DeMott, Paul J.; Elliot, Scott; Facchini, Maria Cristina; Fairall, Chris W.; Hawkins, Lelia; Hu, Yongxiang; Smirnov, Alexander

    2013-01-01

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

  16. Indoor/outdoor radon decay products associated aerosol particle-size distributions and their relation to total number concentrations.

    PubMed

    Moriizumi, Jun; Yamada, Shinya; Xu, Yang; Matsuki, Satoru; Hirao, Shigekazu; Yamazawa, Hiromi

    2014-07-01

    The activity size distributions of indoor and outdoor radioactive aerosol associated with short-lived radon decay products were observed at Nagoya, Japan, for some periods from 2010 to 2012, following the indoor observation by Mostafa et al. [Mostafa, A. M. A., Tamaki, K., Moriizumi, J., Yamazawa, H. and Iida, T. The weather dependence of particle size distribution of indoor radioactive aerosol associated with radon decay products. Radiat. Prot. Dosim. 146: (1-3), 19-22 (2011)]. The tendency of smaller indoor activity median aerodynamic diameter (AMAD) after rainfalls showed in the previous study was not consistently obtained, while the consistent tendency of less indoor radioactive particles with diameters in the accumulation mode was observed again after rainfalls. The indoor aerosols showed activity size distributions similar to the outdoor ones. Non-radioactive aerosol particle concentrations measured with a laser particle counter suggested a somewhat liner relationship with AMAD.

  17. Global Distribution of Cloud Droplet Number Concentration, Autoconversion Rate, and Aerosol Indirect Effect Under Diabatic Droplet Activation

    NASA Technical Reports Server (NTRS)

    Barahona, Donifan; Sotiropoulou, Rafaella; Nenes, Athanasios

    2011-01-01

    This study presents a global assessment of the sensitivity of droplet number to diabatic activation (i.e., including effects from entrainment of dry air) and its first-order tendency on indirect forcing and autoconversion. Simulations were carried out with the NASA Global Modeling Initiative (GMI) atmospheric and transport model using climatological metereorological fields derived from the former NASA Data Assimilation Office (DAO), the NASA Finite volume GCM (FVGCM) and the Goddard Institute for Space Studies version II (GISS) GCM. Cloud droplet number concentration (CDNC) is calculated using a physically based prognostic parameterization that explicitly includes entrainment effects on droplet formation. Diabatic activation results in lower CDNC, compared to adiabatic treatment of the process. The largest decrease in CDNC (by up to 75 percent) was found in the tropics and in zones of moderate CCN concentration. This leads to a global mean effective radius increase between 0.2-0.5 micrometers (up to 3.5 micrometers over the tropics), a global mean autoconversion rate increase by a factor of 1.1 to 1.7 (up to a factor of 4 in the tropics), and a 0.2-0.4 W m(exp -2) decrease in indirect forcing. The spatial patterns of entrainment effects on droplet activation tend to reduce biases in effective radius (particularly in the tropics) when compared to satellite retrievals. Considering the diabatic nature of ambient clouds, entrainment effects on CDNC need to be considered in GCM studies of the aerosol indirect effect.

  18. Simulation of Regional-scale Nucleation Events and Prediction of Aerosol Number Concentration in a Regional Air Quality Model

    NASA Astrophysics Data System (ADS)

    Jung, J.; Adams, P.; Pandis, S.

    2006-12-01

    Nanoparticles can perturb Earth's climate by growing to cloud condensation nuclei sizes and also may be harmful to human health. Accurate simulation of the nucleation, growth, and removal of multicomponent nanoparticles demands enormous computational resources. Most regional-scale three-dimensional chemical transport models do not include nanoparticles and do not conserve number concentrations. A major challenge associated with the simulation of nucleation events is the uncertainty regarding the controlling nucleation mechanism under typical atmospheric conditions. Previous work indicates that nucleation events in the Pittsburgh area are well predicted using ternary (H2O-H2SO4-NH3) nucleation theory, which was successful in predicting on which days nucleation events occurred during summer and winter, as well as the beginning and end of the events. To predict the composition and growth of nanoparticles, we have developed a computationally efficient new approach based on the Two-Moment Aerosol Sectional (TOMAS) microphysics module. This model simulates inorganic and organic components of the nanoparticles describing both the number and the mass distribution of the particulate matter from approximately 1 nm to 10 micrometers. The model explains why nanoparticles were observed to be acidic during nucleation events that appear to involve ammonia. The simulation suggests that nanoparticles produced by ternary nucleation can be acidic due to depletion of ammonia vapor during the growth of the particles out of the nucleation sizes. The low CPU time requirements of the model using TOMAS make it suitable for incorporation in three- dimensional chemical transport models. The nucleation/coagulation/growth model has been added to the PMCAMx regional air quality model and is used for the investigation of nucleation events in the Eastern U.S. We can estimate number budget in the Eastern U.S. and predict frequency/size of nucleation events.

  19. Evidence for anthropogenic impact on number concentration and sulfate content of cloud-processed aerosol particles over the North-Atlantic

    NASA Astrophysics Data System (ADS)

    van Dingenen, Rita; Raes, Frank; Jensen, Niels R.

    1995-10-01

    Aerosol properties were measured during two transects over the North Atlantic between Halifax (Nova Scotia, Canada) and the Moroccan coast. Measurements of the chemical composition of total aerosol, of the black carbon concentration and of the number size distributions with particle diameter Dp in the range 16 nm < Dp < 1 μm were made. The e-folding lifetime of the black carbon aerosol, coming from the northeast American continent and transported eastward over the ocean, was estimated to be 15 hours. The non-sea-salt (nss) fraction of the sulfate concentrations encountered during this campaign spans a 3 order of magnitude range (0.02 μm m-3 to 19 μm m-3) and shows a high correlation with black carbon. The measured bimodal aerosol size distributions were analysed in order to yield number concentrations of the nuclei and the accumulation mode (ACM), the latter being interpreted as cloud-processed particles and thus as cloud condensation nuclei (CCN). A strong positive correlation was found between ACM number concentration and nss-sulfate load over the whole concentration range, i.e. for clean to polluted air masses. Furthermore, our regression between nss-sulfate and ACM number concentration also agrees well with results from other investigators where CCN or cloud droplet concentrations were related to nss-sulfate at a variety of geographical locations and degrees of pollution. The composite data set shows that the nss-sulfate-CCN relationship from baseline conditions to anthropogenically conditioned aerosol, happens via a smooth transition which can be described by a linear regression on a logarithmic scale.

  20. Estimating Marine Aerosol Particle Volume and Number from Maritime Aerosol Network Data

    NASA Technical Reports Server (NTRS)

    Sayer, A. M.; Smirnov, A.; Hsu, N. C.; Munchak, L. A.; Holben, B. N.

    2012-01-01

    As well as spectral aerosol optical depth (AOD), aerosol composition and concentration (number, volume, or mass) are of interest for a variety of applications. However, remote sensing of these quantities is more difficult than for AOD, as it is more sensitive to assumptions relating to aerosol composition. This study uses spectral AOD measured on Maritime Aerosol Network (MAN) cruises, with the additional constraint of a microphysical model for unpolluted maritime aerosol based on analysis of Aerosol Robotic Network (AERONET) inversions, to estimate these quantities over open ocean. When the MAN data are subset to those likely to be comprised of maritime aerosol, number and volume concentrations obtained are physically reasonable. Attempts to estimate surface concentration from columnar abundance, however, are shown to be limited by uncertainties in vertical distribution. Columnar AOD at 550 nm and aerosol number for unpolluted maritime cases are also compared with Moderate Resolution Imaging Spectroradiometer (MODIS) data, for both the present Collection 5.1 and forthcoming Collection 6. MODIS provides a best-fitting retrieval solution, as well as the average for several different solutions, with different aerosol microphysical models. The average solution MODIS dataset agrees more closely with MAN than the best solution dataset. Terra tends to retrieve lower aerosol number than MAN, and Aqua higher, linked with differences in the aerosol models commonly chosen. Collection 6 AOD is likely to agree more closely with MAN over open ocean than Collection 5.1. In situations where spectral AOD is measured accurately, and aerosol microphysical properties are reasonably well-constrained, estimates of aerosol number and volume using MAN or similar data would provide for a greater variety of potential comparisons with aerosol properties derived from satellite or chemistry transport model data.

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

    NASA Astrophysics Data System (ADS)

    Birmili, Wolfram; Weinhold, Kay; Rasch, Fabian; Sonntag, André; Sun, Jia; Merkel, Maik; Wiedensohler, Alfred; Bastian, Susanne; Schladitz, Alexander; Löschau, Gunter; Cyrys, Josef; Pitz, Mike; Gu, Jianwei; Kusch, Thomas; Flentje, Harald; Quass, Ulrich; Kaminski, Heinz; Kuhlbusch, Thomas A. J.; Meinhardt, Frank; Schwerin, Andreas; Bath, Olaf; Ries, Ludwig; Gerwig, Holger; Wirtz, Klaus; Fiebig, Markus

    2016-08-01

    The German Ultrafine Aerosol Network (GUAN) is a cooperative atmospheric observation network, which aims at improving the scientific understanding of aerosol-related effects in the troposphere. The network addresses research questions dedicated to both climate- and health-related effects. GUAN's core activity has been the continuous collection of tropospheric particle number size distributions and black carbon mass concentrations at 17 observation sites in Germany. These sites cover various environmental settings including urban traffic, urban background, rural background, and Alpine mountains. In association with partner projects, GUAN has implemented a high degree of harmonisation of instrumentation, operating procedures, and data evaluation procedures. The quality of the measurement data is assured by laboratory intercomparisons as well as on-site comparisons with reference instruments. This paper describes the measurement sites, instrumentation, quality assurance, and data evaluation procedures in the network as well as the EBAS repository, where the data sets can be obtained (doi:10.5072/guan).

  2. Three years of aerosol mass, black carbon and particle number concentrations at Montsec (southern Pyrenees, 1570 m a.s.l.)

    NASA Astrophysics Data System (ADS)

    Ripoll, A.; Pey, J.; Minguillón, M. C.; Pérez, N.; Pandolfi, M.; Querol, X.; Alastuey, A.

    2014-04-01

    Time variation of mass particulate matter (PM1 and PM1&minus10), black carbon (BC) and number of particles (N3: number of particles with an aerodynamic diameter higher than 3 nm, and N10: higher than 10 nm) concentrations at the high-altitude site of Montsec (MSC) in the southern Pyrenees was interpreted for the period 2010-2012. At MSC, PM10 (12 μg m-3) and N7 (2140 # cm-3) three-year arithmetic average concentrations were higher than those measured at other high-altitude sites in central Europe during the same period (PM10: 3-9 μg m-3 and N: 634-2070 # cm-3). By contrast, BC concentrations at MSC (0.2 μg m-3) were equal to or even lower than those measured at these European sites (0.2-0.4 μg m-3). These differences were attributed to the higher relevance of Saharan dust transport and to the higher importance of the biogenic precursor emissions and new particle formation (NPF) processes, and to the lower influence of anthropogenic emissions at MSC. The different time variation of PM and BC concentrations compared with that of N suggests that these aerosol parameters were governed by diverse factors at MSC. Both PM and BC concentrations showed marked differences for different meteorological scenarios, with enhanced concentrations under North African air outbreaks (PM1&minus10: 13 μg m-3, PM1: 8 μg m-3 and BC: 0.3 μg m-3) and low concentrations when Atlantic advections occurred (PM1-10: 5 μg m-3, PM1: 4 μg m-3 and BC: 0.1 μg m-3). PM and BC concentrations increased in summer, with a secondary maximum in early spring, and were at their lowest in winter, due to the contrasting origin of the air masses in the warmer seasons (spring and summer) and in the colder seasons (autumn and winter). The maximum in the warmer seasons was attributed to long-range transport processes that mask the breezes and regional transport breaking the daily cycles of these pollutants. By contrast, PM and BC concentrations showed clear diurnal cycles, with maxima at midday in the

  3. Three years of aerosol mass, black carbon and particle number concentrations at Montsec (southern~Pyrenees, 1570 m a.s.l.)

    NASA Astrophysics Data System (ADS)

    Ripoll, A.; Pey, J.; Minguillón, M. C.; Pérez, N.; Pandolfi, M.; Querol, X.; Alastuey, A.

    2013-10-01

    Time variation of mass particulate matter (PM1 and PM1-10), black carbon (BC) and particle number (N) concentrations at the high altitude site of Montsec (MSC) in the southern Pyrenees was interpreted for the period 2010-2012. The MSC site registered higher PM10 (12 μg m-3) and N > 7 nm (2209 # cm-3) concentrations than those measured at other high altitude sites in central Europe (PM10: 3-9 μg m-3 and N: 634-2070 # cm-3). By contrast, BC concentrations at MSC (0.2 μg m-3) were equal or even lower than those measured at these European sites (0.2-0.4 μg m-3). These differences were attributed to the lower influence of anthropogenic emissions and to the higher relevance of Saharan dust transport and new particle formation (NPF) processes at MSC. The different time variation of PM and BC concentrations compared with that of N suggests that these aerosol parameters were governed by diverse factors at MSC. Both PM and BC concentrations showed marked differences for different meteorological scenarios, with enhanced concentrations under North African outbreaks (PM1-10: 13 μg m-3, PM1: 8 μg m-3 and BC: 0.3 μg m-3) and low concentrations when Atlantic advections occurred (PM1-10: 5 μg m-3, PM1: 4 μg m-3 and BC: 0.1 μg m-3). Because of the contrasting origin of the air masses in the warmer seasons (spring and summer) and in the colder seasons (autumn and winter), PM and BC concentrations showed a marked increase in summer, with a secondary maximum in early spring, and were at their lowest during winter. The maximum in the warmer seasons was attributed to long-range transport processes which mask the breezes and regional transport breaking the daily cycles of these pollutants. By contrast, PM and BC concentrations showed clear diurnal cycles with maxima at midday in the colder seasons. A statistically significant weekly variation was also obtained for the BC concentrations, displaying a progressive increase from Tuesday to Saturday, followed by a significant

  4. Droplet Number Concentration Value Added Product

    SciTech Connect

    Chitra Sivaraman, PNNL

    2015-08-06

    Cloud droplet number concentration is an important factor in understanding aerosol-cloud interactions. As aerosol concentration increases, it is expected that droplet number concentration (Nd) will increase and droplet size will decrease, for a given liquid water path. This will greatly affect cloud albedo as smaller droplets reflect more shortwave radiation; however, the magnitude and variability of these processes under different environmental conditions is still uncertain.McComiskey et al. (2009) have implemented a method, based onBoers and Mitchell (1994), for calculating Nd from ground-based remote sensing measurements of optical depth and liquid water path. They show that the magnitude of the aerosol-cloud interactions (ACI) varies with a range of factors, including the relative value of the cloud liquid water path (LWP), the aerosol size distribution, and the cloud updraft velocity. Estimates of Nd under a range of cloud types and conditions and at a variety of sites are needed to further quantify the impacts of aerosol cloud interactions. In order to provide data sets for studying aerosol-cloud interactions, the McComiskey et al. (2009) method was implemented as the Droplet Number Concentration (NDROP) value-added product (VAP).

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

    PubMed

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

    2012-02-01

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

  6. High Concentration Standard Aerosol Generator.

    DTIC Science & Technology

    1985-07-31

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

  7. Fog-Influenced Submicron Aerosol Number Size Distributions

    NASA Astrophysics Data System (ADS)

    Zikova, N.; Zdimal, V.

    2013-12-01

    The aim of this work is to evaluate the influence of fog on aerosol particle number size distributions (PNSD) in submicron range. Thus, five-year continuous time series of the SMPS (Scanning Mobility Particle Sizer) data giving information on PNSD in five minute time step were compared with detailed meteorological records from the professional meteorological station Kosetice in the Czech Republic. The comparison included total number concentration and PNSD in size ranges between 10 and 800 nm. The meteorological records consist from the exact times of starts and ends of individual meteorological phenomena (with one minute precision). The records longer than 90 minutes were considered, and corresponding SMPS spectra were evaluated. Evaluation of total number distributions showed considerably lower concentration during fog periods compared to the period when no meteorological phenomenon was recorded. It was even lower than average concentration during presence of hydrometeors (not only fog, but rain, drizzle, snow etc. as well). Typical PNSD computed from all the data recorded in the five years is in Figure 1. Not only median and 1st and 3rd quartiles are depicted, but also 5th and 95th percentiles are plotted, to see the variability of the concentrations in individual size bins. The most prevailing feature is the accumulation mode, which seems to be least influenced by the fog presence. On the contrary, the smallest aerosol particles (diameter under 40 nm) are effectively removed, as well as the largest particles (diameter over 500 nm). Acknowledgements: This work was supported by the projects GAUK 62213 and SVV-2013-267308. Figure 1. 5th, 25th, 50th, 75th and 95th percentile of aerosol particle number size distributions recorded during fog events.

  8. Polarimetric Retrievals of Cloud Droplet Number Concentrations

    NASA Astrophysics Data System (ADS)

    Sinclair, K.; Cairns, B.; Hair, J. W.; Hu, Y.; Hostetler, C. A.

    2014-12-01

    Cloud droplet number concentration (CDNC) is one of the most significant microphysical properties of liquid clouds and is essential for the understanding of aerosol-cloud interaction. It impacts radiative forcing, cloud evolution, precipitation, global climate and, through observation, can be used to monitor the cloud albedo effect, or the first indirect effect. The IPCC's Fifth Assessment Report continues to consider aerosol-cloud interactions as one of the largest uncertainties in radiative forcing of climate. The SABOR experiment, which was a NASA-led ship and air campaign off the east coast of the United States during July and August of 2014, provided an opportunity for the Research Scanning Polarimeter (RSP) to develop and cross-validate a new approach of sensing CDNC with the High Spectral Resolution Lidar (HSRL). The RSP is an airborne prototype of the Aerosol Polarimetry Sensor (APS) that was on-board the Glory satellite. It is a scanning sensor that provides high-precision measurements of polarized and full-intensity radiances at multiple angles over a wide spectral range. The distinctive feature of the polarimetric technique is that it does not make any assumption of the liquid water profile within the cloud. The approach involves (1) estimating the droplet size distribution from polarized reflectance observations in the rainbow, (2) using polarized reflectance to estimate above cloud water vapor and total reflectance to find how much near infra-red light is being absorbed in clouds, (3) finding cloud physical thickness from the absorption and cloud top pressure retrievals assuming a saturated mixing ratio for water vapor and (4) determining the cloud droplet number concentration from the physical thickness and droplet size distribution retrievals. An overview of the polarimetric technique will be presented along with the results of applying the new approach to SABOR campaign data. An analysis of the algorithm's performance when compared with the HSRL

  9. 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.

  10. Characterization of Florida red tide aerosol and the temporal profile of aerosol concentration

    PubMed Central

    Cheng, Yung Sung; Zhou, Yue; Pierce, Richard H.; Henry, Mike; Baden, Daniel G.

    2009-01-01

    Red tide aerosols containing aerosolized brevetoxins are produced during the red tide bloom and transported by wind to coastal areas of Florida. This study reports the characterization of Florida red tide aerosols in human volunteer studies, in which an asthma cohort spent 1 h on Siesta Beach (Sarasota, Florida) during aerosolized red tide events and non-exposure periods. Aerosol concentrations, brevetoxin levels, and particle size distribution were measured. Hourly filter samples were taken and analyzed for brevetoxin and NaCl concentrations. In addition, the aerosol mass concentration was monitored in real time. The results indicated that during a non-exposure period in October 2004, no brevetoxin was detected in the water, resulting in non-detectable levels of brevetoxin in the aerosol. In March 2005, the time-averaged concentrations of brevetoxins in water samples were moderate, in the range of 5–10 μg/L, and the corresponding brevetoxin level of Florida red tide aerosol ranged between 21 and 39 ng/m3. The temporal profiles of red tide aerosol concentration in terms of mass, NaCl, and brevetoxin were in good agreement, indicating that NaCl and brevetoxins are components of the red tide aerosol. By continuously monitoring the marine aerosol and wind direction at Siesta Beach, we observed that the marine aerosol concentration varied as the wind direction changed. The temporal profile of the Florida red tide aerosol during a sampling period could be explained generally with the variation of wind direction. PMID:19879288

  11. Characterization of Florida red tide aerosol and the temporal profile of aerosol concentration.

    PubMed

    Cheng, Yung Sung; Zhou, Yue; Pierce, Richard H; Henry, Mike; Baden, Daniel G

    2010-05-01

    Red tide aerosols containing aerosolized brevetoxins are produced during the red tide bloom and transported by wind to coastal areas of Florida. This study reports the characterization of Florida red tide aerosols in human volunteer studies, in which an asthma cohort spent 1h on Siesta Beach (Sarasota, Florida) during aerosolized red tide events and non-exposure periods. Aerosol concentrations, brevetoxin levels, and particle size distribution were measured. Hourly filter samples were taken and analyzed for brevetoxin and NaCl concentrations. In addition, the aerosol mass concentration was monitored in real time. The results indicated that during a non-exposure period in October 2004, no brevetoxin was detected in the water, resulting in non-detectable levels of brevetoxin in the aerosol. In March 2005, the time-averaged concentrations of brevetoxins in water samples were moderate, in the range of 5-10 microg/L, and the corresponding brevetoxin level of Florida red tide aerosol ranged between 21 and 39 ng/m(3). The temporal profiles of red tide aerosol concentration in terms of mass, NaCl, and brevetoxin were in good agreement, indicating that NaCl and brevetoxins are components of the red tide aerosol. By continuously monitoring the marine aerosol and wind direction at Siesta Beach, we observed that the marine aerosol concentration varied as the wind direction changed. The temporal profile of the Florida red tide aerosol during a sampling period could be explained generally with the variation of wind direction.

  12. Aerosol particle number concentration measurements in five European cities using TSI-3022 condensation particle counter over a three-year period during health effects of air pollution on susceptible subpopulations.

    PubMed

    Aalto, Pasi; Hämeri, Kaarle; Paatero, Pentti; Kulmala, Markku; Bellander, Tom; Berglind, Niklas; Bouso, Laura; Castaño-Vinyals, Gemma; Sunyer, Jordi; Cattani, Giorgio; Marconi, Achille; Cyrys, Josef; von Klot, Stephanie; Peters, Annette; Zetzsche, Katrin; Lanki, Timo; Pekkanen, Juha; Nyberg, Fredrik; Sjövall, Billy; Forastiere, Francesco

    2005-08-01

    In this study, long-term aerosol particle total number concentration measurements in five metropolitan areas across Europe are presented. The measurements have been carried out in Augsburg, Barcelona, Helsinki, Rome, and Stockholm using the same instrument, a condensation particle counter (TSI model 3022). The results show that in all of the studied cities, the winter concentrations are higher than the summer concentrations. In Helsinki and in Stockholm, winter concentrations are higher by a factor of two and in Augsburg almost by a factor of three compared with summer months. The winter maximum of the monthly average concentrations in these cities is between 10,000 cm(-3) and 20,000 cm(-3), whereas the summer min is approximately 5000-6000 cm(-3). In Rome and in Barcelona, the winters are more polluted compared with summers by as much as a factor of 4-10. The winter maximum in both Rome and Barcelona is close to 100,000 cm(-3), whereas the summer minimum is > 10,000 cm(-3). During the weekdays the maximum of the hourly average concentrations in all of the cities is detected during the morning hours between 7 and 10 a.m. The evening maxima were present in Barcelona, Rome, and Augsburg, but these were not as pronounced as the morning ones. The daily maxima in Helsinki and Stockholm are close or even lower than the daily minima in the more polluted cities. The concentrations between these two groups of cities are different with a factor of about five during the whole day. The study pointed out the influence of the selection of the measurement site and the configuration of the sampling line on the observed concentrations.

  13. Improving aerosol distributions below clouds by assimilating satellite-retrieved cloud droplet number

    PubMed Central

    Saide, Pablo E.; Carmichael, Gregory R.; Spak, Scott N.; Minnis, Patrick; Ayers, J. Kirk

    2012-01-01

    Limitations in current capabilities to constrain aerosols adversely impact atmospheric simulations. Typically, aerosol burdens within models are constrained employing satellite aerosol optical properties, which are not available under cloudy conditions. Here we set the first steps to overcome the long-standing limitation that aerosols cannot be constrained using satellite remote sensing under cloudy conditions. We introduce a unique data assimilation method that uses cloud droplet number (Nd) retrievals to improve predicted below-cloud aerosol mass and number concentrations. The assimilation, which uses an adjoint aerosol activation parameterization, improves agreement with independent Nd observations and with in situ aerosol measurements below shallow cumulus clouds. The impacts of a single assimilation on aerosol and cloud forecasts extend beyond 24 h. Unlike previous methods, this technique can directly improve predictions of near-surface fine mode aerosols responsible for human health impacts and low-cloud radiative forcing. Better constrained aerosol distributions will help improve health effects studies, atmospheric emissions estimates, and air-quality, weather, and climate predictions. PMID:22778436

  14. Improving aerosol distributions below clouds by assimilating satellite-retrieved cloud droplet number.

    PubMed

    Saide, Pablo E; Carmichael, Gregory R; Spak, Scott N; Minnis, Patrick; Ayers, J Kirk

    2012-07-24

    Limitations in current capabilities to constrain aerosols adversely impact atmospheric simulations. Typically, aerosol burdens within models are constrained employing satellite aerosol optical properties, which are not available under cloudy conditions. Here we set the first steps to overcome the long-standing limitation that aerosols cannot be constrained using satellite remote sensing under cloudy conditions. We introduce a unique data assimilation method that uses cloud droplet number (N(d)) retrievals to improve predicted below-cloud aerosol mass and number concentrations. The assimilation, which uses an adjoint aerosol activation parameterization, improves agreement with independent N(d) observations and with in situ aerosol measurements below shallow cumulus clouds. The impacts of a single assimilation on aerosol and cloud forecasts extend beyond 24 h. Unlike previous methods, this technique can directly improve predictions of near-surface fine mode aerosols responsible for human health impacts and low-cloud radiative forcing. Better constrained aerosol distributions will help improve health effects studies, atmospheric emissions estimates, and air-quality, weather, and climate predictions.

  15. ARM Evaluation Product : Droplet Number Concentration Value-Added Product

    DOE Data Explorer

    Riihimaki, Laura

    2014-05-15

    Cloud droplet number concentration is an important factor in understanding aerosol-cloud interactions. As aerosol concentration increases, it is expected that droplet number concentration, Nd, will increase and droplet size decrease, for a given liquid water path (Twomey 1977), which will greatly affect cloud albedo as smaller droplets reflect more shortwave radiation. However, the magnitude and variability of these processes under different environmental conditions is still uncertain. McComiskey et al. (2009) have implemented a method, based on Boers and Mitchell (1994), for calculating Nd from ground-based remote sensing measurements of optical depth and liquid water path. They show that the magnitude of the aerosol-cloud interactions (ACI) varies with a range of factors, including the relative value of the cloud liquid water path (LWP), the aerosol size distribution, and the cloud updraft velocity. Estimates of Nd under a range of cloud types and conditions and at a variety of sites are needed to further quantify the impacts of aerosol cloud interactions.

  16. 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.

  17. Unexpectedly high ultrafine aerosol concentrations above East Antarctic sea ice

    NASA Astrophysics Data System (ADS)

    Humphries, R. S.; Klekociuk, A. R.; Schofield, R.; Keywood, M.; Ward, J.; Wilson, S. R.

    2016-02-01

    Better characterisation of aerosol processes in pristine, natural environments, such as Antarctica, have recently been shown to lead to the largest reduction in uncertainties in our understanding of radiative forcing. Our understanding of aerosols in the Antarctic region is currently based on measurements that are often limited to boundary layer air masses at spatially sparse coastal and continental research stations, with only a handful of studies in the vast sea-ice region. In this paper, the first observational study of sub-micron aerosols in the East Antarctic sea ice region is presented. Measurements were conducted aboard the icebreaker Aurora Australis in spring 2012 and found that boundary layer condensation nuclei (CN3) concentrations exhibited a five-fold increase moving across the polar front, with mean polar cell concentrations of 1130 cm-3 - higher than any observed elsewhere in the Antarctic and Southern Ocean region. The absence of evidence for aerosol growth suggested that nucleation was unlikely to be local. Air parcel trajectories indicated significant influence from the free troposphere above the Antarctic continent, implicating this as the likely nucleation region for surface aerosol, a similar conclusion to previous Antarctic aerosol studies. The highest aerosol concentrations were found to correlate with low-pressure systems, suggesting that the passage of cyclones provided an accelerated pathway, delivering air masses quickly from the free troposphere to the surface. After descent from the Antarctic free troposphere, trajectories suggest that sea-ice boundary layer air masses travelled equatorward into the low-albedo Southern Ocean region, transporting with them emissions and these aerosol nuclei which, after growth, may potentially impact on the region's radiative balance. The high aerosol concentrations and their transport pathways described here, could help reduce the discrepancy currently present between simulations and observations of

  18. Design and Fabrication of an Aerosol Concentrator.

    DTIC Science & Technology

    1980-05-08

    MBEran GpVt 08C IO NO 3. RECIPIENT’S CATALOG NUMBER 4. TITL S. VVIREOP ePORT A PERIOD COVERED Interim report on a continuing ~ESIGN AND ,BRICATION OF AN...electronic tachometer , and a variable speed controller. Our motor is a hand-held router motor, model 90114, manufactured by the Stanley Power Tool Company (P.O...be obtained from Lordco Supply (Erie, PA 16505). Since the concentrator is run at various speeds, we incorporated an electronic tachometer into the

  19. Concentration, sources, and degradation of organic aerosol at Summit, Greenland

    NASA Astrophysics Data System (ADS)

    von Schneidemesser, Erika

    Characterization and understanding of the carbonaceous portion of the aerosol in the Arctic is limited. The objective of the research presented in this thesis was to improve the scope of knowledge pertaining to carbonaceous aerosols, in terms of atmospheric and snow concentrations, sources, and post-depositional processing. An extraction technique was developed to quantitatively identify a suite of organic compounds, typically observed in aerosol samples, at trace level concentrations in snow melt water samples. A field campaign of sampling and exposure experiments was carried out at Summit, Greenland. A 3-meter snow pit, sampled at 20 cm intervals, was analyzed for organic compounds and total organic carbon (TOC). The average concentration of TOC for the entire pit was 64 mug C kg-1. The quantified organic compounds comprised 6 to 24% of TOC throughout the layers. Median concentrations of the water insoluble individual organic compounds ranged from 0.14 ng kg-1 (hopane) to 2200 ng kg-1 (alkanoic acid) at any one depth. High-volume aerosol samples were collected over a six month period and analyzed for organics. Median concentrations ranged from 0.00045 ng kg-1 (hopane) to 0.23 ng kg-1 (levoglucosan) in the air samples. Source apportionment results from the aerosol samples indicate anthropogenic influence at Summit from biomass burning, fossil fuels, and vegetative detritus. The majority (>90%) of the organic carbon in the aerosol was estimated to be secondary organic aerosol. To investigate the post-depositional processing of organic compounds in snow, contaminant labeled snow was produced and exposed for up to 72 hours on the surface of the Greenland ice sheet at Summit. Degradation of alkanes, acids, and PAHs to a threshold concentration was observed. The threshold concentration, at which no further degradation was observed, ranged from 10 to 60% of the original (non-exposed) snow concentrations, depending on the reaction rate. This would indicate that a

  20. Recent Field Measurements of Ice Nuclei Concentration Relation to Aerosol Properties

    NASA Astrophysics Data System (ADS)

    DeMott, P. J.; Sullivan, R. C.; McMeeking, G.; Prenni, A. J.; Hill, T. C.; Franc, G. D.; Sullivan, A. P.; Garcia, E.; Tobo, Y.; Prather, K. A.; Suski, K.; Cazorla, A.; Anderson, J. R.; Kreidenweis, S. M.

    2011-12-01

    It is expected that atmospheric variability of ice nuclei concentrations is governed by a variety of factors related to aerosol physical and chemical properties. Not all particles contribute equally due to the special nature of ice nuclei. The "size requirement" of ice nuclei (Pruppacher and Klett, 1997), partly related to the typical aerosol compositions known to act as ice nuclei (e.g., mineral dust particles, certain biological particles), leads to the relation of ice nuclei number concentrations to larger aerosol concentrations in some cases, but we emphasize here the additional relation to aerosol chemistry. Recent atmospheric ice nuclei measurements focused on biomass burning, mineral dust, pollution and biological particles will be discussed to highlight new assessment of their source contributions on the basis of physical, chemical and biological analysis. Pruppacher, H. R., and J. D. Klett, 1997: Microphysics of Clouds and Precipitation (2nd Edition), Kluwer Academic Press, Dordrecht, 954 pp.

  1. The importance of aerosol composition and mixing state on predicted CCN concentration and the variation of the importance with atmospheric processing of aerosol

    SciTech Connect

    Wang, J.; Cubison, M.; Aiken, A.; Jimenez, J.; Collins, D.; Gaffney, J.; Marley, N.

    2010-03-15

    The influences of atmospheric aerosols on cloud properties (i.e., aerosol indirect effects) strongly depend on the aerosol CCN concentrations, which can be effectively predicted from detailed aerosol size distribution, mixing state, and chemical composition using Köhler theory. However, atmospheric aerosols are complex and heterogeneous mixtures of a large number of species that cannot be individually simulated in global or regional models due to computational constraints. Furthermore, the thermodynamic properties or even the molecular identities of many organic species present in ambient aerosols are often not known to predict their cloud-activation behavior using Köhler theory. As a result, simplified presentations of aerosol composition and mixing state are necessary for large-scale models. In this study, aerosol microphysics, CCN concentrations, and chemical composition measured at the T0 urban super-site in Mexico City during MILAGRO are analyzed. During the campaign in March 2006, aerosol size distribution and composition often showed strong diurnal variation as a result of both primary emissions and aging of aerosols through coagulation and local photochemical production of secondary aerosol species. The submicron aerosol composition was ~1/2 organic species. Closure analysis is first carried out by comparing CCN concentrations calculated from the measured aerosol size distribution, mixing state, and chemical composition using extended Köhler theory to concurrent CCN measurements at five supersaturations ranging from 0.11% to 0.35%. The closure agreement and its diurnal variation are studied. CCN concentrations are also derived using various simplifications of the measured aerosol mixing state and chemical composition. The biases associated with these simplifications are compared for different supersaturations, and the variation of the biases is examined as a function of aerosol age. The results show that the simplification of internally mixed, size

  2. Decreasing particle number concentrations in a warming atmosphere and implications

    NASA Astrophysics Data System (ADS)

    Yu, F.; Luo, G.; Turco, R. P.; Ogren, J. A.; Yantosca, R. M.

    2011-10-01

    New particle formation contributes significantly to the number concentration of condensation nuclei (CN) as well as cloud CN (CCN), a key factor determining aerosol indirect radiative forcing of the climate system. Using a physics-based nucleation mechanism that is consistent with a range of field observations of aerosol formation, it is shown that projected increases in global temperatures could significantly inhibit new particle, and CCN, formation rates worldwide. An analysis of CN concentrations observed at four NOAA ESRL/GMD baseline stations since the 1970s and two other sites since 1990s reveals long-term decreasing trends consistent with these predictions. The analysis also suggests, owing to larger observed CN reductions at remote sites than can be explained by the basic nucleation mechanism, that dimethylsulphide (DMS) emissions may be decreasing worldwide with increasing global temperatures, implying a positive DMS-based cloud feedback forcing of the climate ("CLAW"). The combined effects of rising temperatures on aerosol nucleation rates, and possibly on DMS emissions, may imply substantial decreases in future tropospheric particle abundances associated with global warming, delineating a potentially significant feedback mechanism that increases Earth's climate sensitivity to greenhouse gas emissions. Further research is needed to quantify the magnitude of such a feedback process.

  3. Decreasing particle number concentrations in a warming atmosphere and implications

    NASA Astrophysics Data System (ADS)

    Yu, F.; Luo, G.; Turco, R. P.; Ogren, J. A.; Yantosca, R. M.

    2012-03-01

    New particle formation contributes significantly to the number concentration of condensation nuclei (CN) as well as cloud CN (CCN), a key factor determining aerosol indirect radiative forcing of the climate system. Using a physics-based nucleation mechanism that is consistent with a range of field observations of aerosol formation, it is shown that projected increases in global temperatures could significantly inhibit new particle, and CCN, formation rates worldwide. An analysis of CN concentrations observed at four NOAA ESRL/GMD baseline stations since the 1970s and two other sites since 1990s reveals long-term decreasing trends that are consistent in sign with, but are larger in magnitude than, the predicted temperature effects. The possible reasons for larger observed long-term CN reductions at remote sites are discussed. The combined effects of rising temperatures on aerosol nucleation rates and other chemical and microphysical processes may imply substantial decreases in future tropospheric particle abundances associated with global warming, delineating a potentially significant feedback mechanism that increases Earth's climate sensitivity to greenhouse gas emissions. Further research is needed to quantify the magnitude of such a feedback process.

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

    NASA Astrophysics Data System (ADS)

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

    2015-12-01

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

  5. Characterization of a Quadrotor Unmanned Aircraft System for Aerosol-Particle-Concentration Measurements.

    PubMed

    Brady, James M; Stokes, M Dale; Bonnardel, Jim; Bertram, Timothy H

    2016-02-02

    High-spatial-resolution, near-surface vertical profiling of atmospheric chemical composition is currently limited by the availability of experimental platforms that can sample in constrained environments. As a result, measurements of near-surface gradients in trace gas and aerosol particle concentrations have been limited to studies conducted from fixed location towers or tethered balloons. Here, we explore the utility of a quadrotor unmanned aircraft system (UAS) as a sampling platform to measure vertical and horizontal concentration gradients of trace gases and aerosol particles at high spatial resolution (1 m) within the mixed layer (0-100 m). A 3D Robotics Iris+ autonomous quadrotor UAS was outfitted with a sensor package consisting of a two-channel aerosol optical particle counter and a CO2 sensor. The UAS demonstrated high precision in both vertical (±0.5 m) and horizontal positions (±1 m), highlighting the potential utility of quadrotor UAS drones for aerosol- and trace-gas measurements within complex terrain, such as the urban environment, forest canopies, and above difficult-to-access areas such as breaking surf. Vertical profiles of aerosol particle number concentrations, acquired from flights conducted along the California coastline, were used to constrain sea-spray aerosol-emission rates from coastal wave breaking.

  6. Process evaluation of sea salt aerosol concentrations at remote marine locations

    NASA Astrophysics Data System (ADS)

    Struthers, H.; Ekman, A. M.; Nilsson, E. D.

    2011-12-01

    Sea salt, an important natural aerosol, is generated by bubbles bursting at the surface of the ocean. Sea salt aerosol contributes significantly to the global aerosol burden and radiative budget and are a significant source of cloud condensation nuclei in remote marine areas (Monahan et al., 1986). Consequently, changes in marine aerosol abundance is expected to impact on climate forcing. Estimates of the atmospheric burden of sea salt aerosol mass derived from chemical transport and global climate models vary greatly both in the global total and the spatial distribution (Texor et al. 2006). This large uncertainty in the sea salt aerosol distribution in turn contributes to the large uncertainty in the current estimates of anthropogenic aerosol climate forcing (IPCC, 2007). To correctly attribute anthropogenic climate change and to veraciously project future climate, natural aerosols including sea salt must be understood and accurately modelled. In addition, the physical processes that determine the sea salt aerosol concentration are susceptible to modification due to climate change (Carslaw et al., 2010) which means there is the potential for feedbacks within the climate/aerosol system. Given the large uncertainties in sea salt aerosol modelling, there is an urgent need to evaluate the process description of sea salt aerosols in global models. An extremely valuable source of data for model evaluation is the long term measurements of PM10 sea salt aerosol mass available from a number of remote marine observation sites around the globe (including the GAW network). Sea salt aerosol concentrations at remote marine locations depend strongly on the surface exchange (emission and deposition) as well as entrainment or detrainment to the free troposphere. This suggests that the key parameters to consider in any analysis include the sea surface water temperature, wind speed, precipitation rate and the atmospheric stability. In this study, the sea salt aerosol observations

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

    PubMed

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

    2003-08-01

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

  8. Source contributions to carbonaceous aerosol concentrations in Korea

    NASA Astrophysics Data System (ADS)

    Jeong, Jaein I.; Park, Rokjin J.; Woo, Jung-Hun; Han, Young-Ji; Yi, Seung-Muk

    2011-02-01

    We estimated the source contributions to carbonaceous aerosol concentration in Korea on the basis of Intercontinental Chemical Transport Experiment Phase B (INTEX-B) anthropogenic emissions and satellite-derived biomass burning emissions by using a nested version of GEOS-Chem with a spatial resolution of 0.5° × 0.667° for the period March 2006-February 2007. First, we evaluated the model by comparing the simulated and observed aerosol concentrations at East Asia Network (EANET) sites and at a site in Korea. The results indicate that the model reproduces the variability and magnitudes of the observed SO 42-, NO 3-, and NH 4+ concentrations in Korea and those of the observed PM 10 concentrations in East Asia. However, the organic carbon (OC) and black carbon (BC) aerosol concentrations estimated by the model are lower than those observed in Korea by a factor of 2, especially in winter. This underestimation is likely due to extremely low domestic anthropogenic emissions and lack in seasonal variation. Source adjustments using a simple fitting and the Emission Database for Global Atmospheric Research (EDGAR) monthly allocation factors for seasonal variation yield significantly improved model results ( R2 increased from 0.58 to 0.84), which can then be used to estimate the source contributions to the OC and BC concentrations in Korea. We found that domestic anthropogenic emissions are the most important factors, contributing 74% (9% from fossil fuels and 65% from biofuels) and 78% (42% from fossil fuels and 36% from biofuels) to the OC and BC concentrations, respectively, on an annual mean basis in Korea. The trans-boundary transport of Chinese sources is another important factor, contributing 13% and 20% to the OC and BC concentrations, respectively. The contributions of wildfires and biogenic sources to the annual mean carbonaceous aerosol concentration in Korea are relatively small (4% and 6%, respectively).

  9. Size and concentration measurement of an industrial aerosol

    SciTech Connect

    O'Brien, D.; Baron, P.; Willeke, K.

    1986-07-01

    Several real-time particle sizing instruments were evaluated for measuring the size distribution and concentration of the aerosol produced during the high speed grinding of gray iron castings. Aerosol was sampled in the airstream entrained by the motion of a spinning grinding wheel in a pilot grinding operation. Measurement methods based on differing physical principles were selected for evaluation and compared: particle inertia (aerodynamic particle sizer and quartz crystal microbalance cascade impactor); light scattering (laser aerosol spectrometer); and projected-area microscopy (scanning electron microscope). Inferences of aerodynamic diameter based on measurements by the laser aerosol spectrometer consistently undersized that determined by the aerodynamic particle sizer by a factor of 1.5. Estimates of aerodynamic diameters from projected area diameters determined by scanning electron microscopy differed from those obtained by the aerodynamic particle sizer by a factor of 2. Differences appeared to be a non-linear function of particle diameter. Estimates of respirable mass determined from mass-weighted particle size spectra varied by a factor of 6 between the largest estimate (scanning electron microscope) and the smallest estimate (laser aerosol spectrometer).

  10. Size and concentration measurement of an industrial aerosol.

    PubMed

    O'Brien, D; Baron, P; Willeke, K

    1986-07-01

    Several real-time particle sizing instruments were evaluated for measuring the size distribution and concentration of the aerosol produced during the high speed grinding of gray iron castings. Aerosol was sampled in the airstream entrained by the motion of a spinning grinding wheel in a pilot grinding operation. Measurement methods based on differing physical principles were selected for evaluation and compared: particle inertia (aerodynamic particle sizer and quartz crystal microbalance cascade impactor); light scattering (laser aerosol spectrometer); and projected-area microscopy (scanning electron microscope). Inferences of aerodynamic diameter based on measurements by the laser aerosol spectrometer consistently undersized that determined by the aerodynamic particle sizer by a factor of 1.5. Estimates of aerodynamic diameters from projected area diameters determined by scanning electron microscopy differed from those obtained by the aerodynamic particle sizer by a factor of 2. Differences appeared to be a non-linear function of particle diameter. Estimates of respirable mass determined from mass-weighted particle size spectra varied by a factor of 6 between the largest estimate (scanning electron microscope) and the smallest estimate (laser aerosol spectrometer).

  11. Concentration Effects on the Thermophoresis of Aerosol Spheres.

    PubMed

    Keh; Ho

    1999-08-01

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

  12. Concentrations and size distributions of Antarctic stratospheric aerosols

    NASA Technical Reports Server (NTRS)

    Ferry, G. V.; Pueschel, R. F.; Neish, E.; Schultz, M.

    1989-01-01

    Particle Measuring Systems laser particle spectrometer (ASAS-X and FSSP) probes were used to measure aerosol particle concentrations and size distributions during 11 ER-2 flights between Punta Arenas (53 deg S) and Antarctica (up to 72 deg S) from August 17 to September 22, 1987. The time resolution was 10 s, corresponding to a spatial resolution of 2 km. The data were divided into two size classes (0.05-0.25 and 0.53-5.5 micron radius) to separate the small particle from the coarse particle populations. Results show that the small-particle concentrations are typical for a background aerosol during volcanic quiescence. This concentration is generally constant along a flight track; in only one instance a depletion of small particles during a polar stratospheric cloud (PSC) encounter was measured, suggesting a nucleation of type I PSC particles on background aerosols. Temporary increases of the coarse particle concentrations indicated the presence of tenuous polar stratospheric clouds that were encountered most frequently at the southernmost portion of a flight track and when the aircraft descended to lower altitudes. During 'particle events', particle modes were found at 0.6-micron radius, corresponding to type I PSCs, and occasionally, at 2.0-micron radius corresponding to type II PSCs.

  13. Relationship Between Aerosol Number Size Distribution and Atmospheric Electric Potential Gradient in an Urban Area

    NASA Astrophysics Data System (ADS)

    Wright, Matthew; Matthews, James; Bacak, Asan; Silva, Hugo; Priestley, Michael; Percival, Carl; Shallcross, Dudley

    2016-04-01

    Small ions are created in the atmosphere by ground based radioactive decay and solar and cosmic radiation ionising the air. The ionosphere is maintained at a high potential relative to the Earth due to global thunderstorm activity, a current from the ionosphere transfers charge back to the ground through the weakly ionised atmosphere. A potential gradient (PG) exists between the ionosphere and the ground that can be measured in fair weather using devices such as an electric field mill. PG is inversely-proportional to the conductivity of the air and therefore to the number of ions of a given electrical mobility; a reduction of air ions will cause an increase of PG. Aerosols in the atmosphere act as a sink of air ions with an attachment rate dependent on aerosol size distribution and ion mobility. These relationships have been used to infer high particulate, and hence pollution, levels in historic datasets of atmospheric PG. A measurement campaign was undertaken in Manchester, UK for three weeks in July and August where atmospheric PG was measured with an electric field mill (JCI131, JCI Chilworth) on a second floor balcony, aerosol size distribution measured with a scanning mobility particle sizer (SMPS, TSI3936), aerosol concentration measured with a condensation particle counter (CPC, Grimm 5.403) and local meteorological measurements taken on a rooftop measurement site ~200 m away. Field mill and CPC data were taken at 1 s intervals and SMPS data in 2.5 minute cycles. Data were excluded for one hour either side of rainfall as rainclouds and droplets can carry significant charge which would affect PG. A quantity relating to the attachment of ions to aerosol (Ion Sink) was derived from the effective attachment coefficient of the aerosols. Further measurements with the field mill and CPC were taken at the same location in November 2015 when bonfire events would be expected to increase aerosol concentrations. During the summer measurements, particle number count (PNC

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

    PubMed

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

    2011-01-01

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

  15. Vertical profiles of black carbon concentration and particle number size distribution in the North China Plain

    NASA Astrophysics Data System (ADS)

    Ran, L.; Deng, Z.

    2013-12-01

    The vertical distribution of aerosols is of great importance to our understanding in the impacts of aerosols on radiation balance and climate, as well as air quality and public health. To better understand and estimate the effects of atmospheric components including trace gases and aerosols on atmospheric environment and climate, an intensive field campaign, Vertical Observations of trace Gases and Aerosols in the North China Plain (VOGA-NCP), was carried out from late July to early August 2013 over a rural site in the polluted NCP. During the campaign, vertical profiles of black carbon (BC) concentration and particle number size distribution were measured respectively by a micro-Aethalometer and an optical particle counter attached to a tethered balloon within 1000 m height. Meteorological parameters, including temperature, relative humidity, wind speed and wind direction, were measured simultaneously by a radiosonde also attached to the tethered balloon. Preliminary results showed distinct diurnal variations of the vertical distribution of aerosol total number concentration and BC concentration, following the development of the mixing layer. Generally, there was a well mixing of aerosols within the mixing layer and a sharp decrease above the mixing layer. Particularly, a small peak of BC concentrations was observed around 400-500 m height for several profiles. Further analysis would be needed to explain such phenomenon. It was also found that measured vertical profiles of BC using the filter-based method might be affected by the vertical distribution of relative humidity.

  16. Droplet Number Concentration Value-Added Product

    SciTech Connect

    Riihimaki, L.; McFarlane, S.; Sivaraman, C.

    2014-06-01

    The ndrop_mfrsr value-added product (VAP) provides an estimate of the cloud droplet number concentration of overcast water clouds retrieved from cloud optical depth from the multi-filter rotating shadowband radiometer (MFRSR) instrument and liquid water path (LWP) retrieved from the microwave radiometer (MWR). When cloud layer information is available from vertically pointing lidar and radars in the Active Remote Sensing of Clouds (ARSCL) product, the VAP also provides estimates of the adiabatic LWP and an adiabatic parameter (beta) that indicates how divergent the LWP is from the adiabatic case. quality control (QC) flags (qc_drop_number_conc), an uncertainty estimate (drop_number_conc_toterr), and a cloud layer type flag (cloud_base_type) are useful indicators of the quality and accuracy of any given value of the retrieval. Examples of these major input and output variables are given in sample plots in section 6.0.

  17. Aerosol formation by ozonolysis of α- and β-pinene with initial concentrations below 1 ppb

    NASA Astrophysics Data System (ADS)

    Saathoff, Harald; Naumann, Karl-Heinz; Möhler, Ottmar

    2014-05-01

    Secondary organic aerosols (SOA) from the oxidation of biogenic volatile organic compounds (BVOC) are a large fraction of the tropospheric aerosol especially over tropical continental regions. The dominant SOA forming compounds are monoterpenes of which pinene is the most abundant. The reactions of monoterpenes with OH radicals, NO3 radicals, and ozone yield secondary organic aerosol mass in highly variable yields. Despite the various studies on SOA formation the influence of temperature and precursor concentrations on SOA yields are still major uncertainties in tropospheric aerosol models. In previous studies we observed a negative temperature dependence of SOA yields for SOA from ozonolysis α-pinene and limonene (Saathoff et al., 2009). However, this study as well as most of the literature data for measured SOA yields is limited to terpene concentrations of several ppb and higher (e.g. Bernard et al., 2012), hence about an order of magnitude higher than terpene concentrations even near their sources. Monoterpene concentrations in and above tropical or boral forests reach values up to a few tenth of a ppb during daytime decreasing rapidly with altitude in the boundary layer (Kesselmeier et al. 2000; Boy et al., 2004). Therefore we investigated the yield of SOA material from the ozonolysis of α- and β-pinene under simulated tropospheric conditions in the large aerosol chamber AIDA on time scales of several hours and for terpene concentrations between 0.1 and 1 ppb. The temperatures investigated were 243, 274, and 296 K with relative humidities ranging from 25% to 41%. The organic aerosol was generated by controlled oxidation with an excess of ozone (220-930 ppb) and the aerosol yield is calculated from size distributions measured with differential mobility analysers (SMPS, TSI, 3071 & 3080N) in the size range between 2 and 820 nm. On the basis of the measured initial particle size distribution, particle number concentration (CPC, TSI, 3775, 3776, 3022), and

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

    NASA Astrophysics Data System (ADS)

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

    2015-04-01

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

  19. Urban background levels of particle number concentration and sources in Vilnius, Lithuania

    NASA Astrophysics Data System (ADS)

    Byčenkienė, Steigvilė; Plauškaitė, Kristina; Dudoitis, Vadimas; Ulevicius, Vidmantas

    2014-06-01

    This study presents results of research on urban aerosol particles with a focus on the aerosol particle number concentration (PNC) and the particle size distribution. The real time measurements of aerosol PNC (> 4.5 nm) and number size distributions (9-840 nm) were performed. The seasonal variations essentially comprised the minimum monthly mean in October 2010 (3400 ± 3000 cm- 3) and the maximum in April 2011 (19,000 ± 15,000 cm- 3). The mean annual PNC was 10,000 ± 8000 cm- 3 with an average mode size of 30-50 nm. The presence of strong diurnal patterns in aerosol PNC was evident as a direct effect of three sources of aerosol particles (nucleation, traffic, and residential heating). Hybrid receptor modeling potential source contribution function (PSCF) and concentration weighted trajectory (CWT) were used by incorporating 72-h backward trajectories and measurements of PNC in Vilnius. The results of trajectory clustering and the PSCF method demonstrated that possible additional source areas contributing to the elevated particle number concentration in Vilnius could be industrial areas in central Europe. Principal component analysis (PCA) revealed highest loadings for PNC, PM10, NOx, NO, NO2 and SO2 concentrations, indicating combustion processes occurring in vehicle engines and use of sulfur-containing fossil fuels for residential heating.

  20. Aerosol concentration and size distribution measured below, in, and above cloud from the DOE G-1 during VOCALS-REx

    SciTech Connect

    Kleinman L. I.; Daum, P. H.; Lee, Y.-N.; Lewis, E. R.; Sedlacek III, A. J.; Senum, G. I.; Springston, S. R.; Wang, J.; Hubbe, J.; Jayne, J.; Min, Q.; Yum, S. S.; Allen, G.

    2012-01-04

    During the VOCALS Regional Experiment, the DOE G-1 aircraft was used to sample a varying aerosol environment pertinent to properties of stratocumulus clouds over a longitude band extending 800 km west from the Chilean coast at Arica. Trace gas and aerosol measurements are presented as a function of longitude, altitude, and dew point in this study. Spatial distributions are consistent with an upper atmospheric source for O{sub 3} and South American coastal sources for marine boundary layer (MBL) CO and aerosol, most of which is acidic sulfate. Pollutant layers in the free troposphere (FT) can be a result of emissions to the north in Peru or long range transport from the west. At a given altitude in the FT (up to 3 km), dew point varies by 40 C with dry air descending from the upper atmospheric and moist air having a boundary layer (BL) contribution. Ascent of BL air to a cold high altitude results in the condensation and precipitation removal of all but a few percent of BL water along with aerosol that served as CCN. Thus, aerosol volume decreases with dew point in the FT. Aerosol size spectra have a bimodal structure in the MBL and an intermediate diameter unimodal distribution in the FT. Comparing cloud droplet number concentration (CDNC) and pre-cloud aerosol (D{sub p} > 100 nm) gives a linear relation up to a number concentration of {approx}150 cm{sup -3}, followed by a less than proportional increase in CDNC at higher aerosol number concentration. A number balance between below cloud aerosol and cloud droplets indicates that {approx}25 % of aerosol with D{sub p} > 100 nm are interstitial (not activated). A direct comparison of pre-cloud and in-cloud aerosol yields a higher estimate. Artifacts in the measurement of interstitial aerosol due to droplet shatter and evaporation are discussed. Within each of 102 constant altitude cloud transects, CDNC and interstitial aerosol were anti-correlated. An examination of one cloud as a case study shows that the

  1. Black Carbon Concentration from Worldwide Aerosol Robotic Network (AERONET)

    NASA Technical Reports Server (NTRS)

    Schuster, Greg; Dubovik, Oleg; Holben, Brent; Clothiaux, Eugene

    2008-01-01

    Worldwide black carbon concentration measurements are needed to assess the efficacy of the carbon emissions inventory and transport model output. This requires long-term measurements in many regions, as model success in one region or season does not apply to all regions and seasons. AERONET is an automated network of more than 180 surface radiometers located throughout the world. The sky radiance measurements obtained by AERONET are inverted to provide column-averaged aerosol refractive indices and size distributions for the AERONET database, which we use to derive column-averaged black carbon concentrations and specific absorptions that are constrained by the measured radiation field. This provides a link between AERONET sky radiance measurements and the elemental carbon concentration of transport models without the need for an optics module in the transport model. Knowledge of both the black carbon concentration and aerosol absorption optical depth (i.e., input and output of the optics module) will enable improvements to the transport model optics module.

  2. Physicochemical characterization of Capstone depleted uranium aerosols I: uranium concentration in aerosols as a function of time and particle size.

    PubMed

    Parkhurst, Mary Ann; Cheng, Yung Sung; Kenoyer, Judson L; Traub, Richard J

    2009-03-01

    During the Capstone Depleted Uranium (DU) Aerosol Study, aerosols containing DU were produced inside unventilated armored vehicles (i.e., Abrams tanks and Bradley Fighting Vehicles) by perforation with large-caliber DU penetrators. These aerosols were collected and characterized, and the data were subsequently used to assess human health risks to personnel exposed to DU aerosols. The DU content of each aerosol sample was first quantified by radioanalytical methods, and selected samples, primarily those from the cyclone separator grit chambers, were analyzed radiochemically. Deposition occurred inside the vehicles as particles settled on interior surfaces. Settling rates of uranium from the aerosols were evaluated using filter cassette samples that collected aerosol as total mass over eight sequential time intervals. A moving filter was used to collect aerosol samples over time, particularly within the first minute after a shot. The results demonstrate that the peak uranium concentration in the aerosol occurred in the first 10 s after perforation, and the concentration decreased in the Abrams tank shots to about 50% within 1 min and to less than 2% after 30 min. The initial and maximum uranium concentrations were lower in the Bradley vehicle than those observed in the Abrams tank, and the concentration levels decreased more slowly. Uranium mass concentrations in the aerosols as a function of particle size were evaluated using samples collected in a cyclone sampler, which collected aerosol continuously for 2 h after perforation. The percentages of uranium mass in the cyclone separator stages ranged from 38 to 72% for the Abrams tank with conventional armor. In most cases, it varied with particle size, typically with less uranium associated with the smaller particle sizes. Neither the Abrams tank with DU armor nor the Bradley vehicle results were specifically correlated with particle size and can best be represented by their average uranium mass concentrations of 65

  3. Number size distribution measurements of biological aerosols under contrasting environments and seasons from southern tropical India

    NASA Astrophysics Data System (ADS)

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

    2016-04-01

    Biological aerosols constitute a wide range of dead and alive biological materials and structures that are suspended in the atmosphere. They play an important role in the atmospheric physical, chemical and biological processes and health of living being by spread of diseases among humans, plants, and, animals. The atmospheric abundance, sources, physical properties of PBAPs as compared to non-biological aerosols, however, is poorly characterized. Though omnipresent, their concentration and composition exhibit large spatial and temporal variations depending up on their sources, land-use, and local meteorology. The Indian tropical region, which constitutes approximately 18% of the world's total population exhibits vast geographical extend and experiences a distinctive meteorological phenomenon by means of Indian Summer Monsoon (IMS). Thus, the sources, properties and characteristics of biological aerosols are also expected to have significant variations over the Indian subcontinent depending upon the location and seasons. Here we present the number concentration and size distribution of Fluorescent Biological Aerosol Particles (FBAP) from two contrasting locations in Southern tropical India measured during contrasting seasons using Ultra Violet Aerodynamic Particle Sizer (UV-APS). Measurements were carried out at a pristine high altitude continental site, Munnar (10.09 N, 77.06 E; 1605 m asl) during two contrasting seasons, South-West Monsoon (June-August, 2014) and winter (Jan - Feb, 2015) and in Chennai, a coastal urban area, during July - November 2015. FBAP concentrations at both the locations showed large variability with higher concentrations occurring at Chennai. Apart from regional variations, the FBAP concentrations also exhibited variations over two different seasons under the same environmental condition. In Munnar the FBAP concentration increased by a factor of four from South-West Monsoon to winter season. The average size distribution of FBAP at both

  4. Aerosol concentration and size distribution measured below, in, and above cloud from the DOE G-1 during VOCALS-REx

    SciTech Connect

    Kleinman, L.I.; Daum, P. H.; Lee, Y.-N.; Lewis, E. R.; Sedlacek III, A. J.; Senum, G. I.; Springston, S. R.; Wang, J.; Hubbe, J.; Jayne, J.; Min, Q.; Yum, S. S.; Allen, G.

    2011-06-21

    During the VOCALS Regional Experiment, the DOE G-1 aircraft was used to sample a varying aerosol environment pertinent to properties of stratocumulus clouds over a longitude band extending 800 km west from the Chilean coast at Arica. Trace gas and aerosol measurements are presented as a function of longitude, altitude, and dew point in this study. Spatial distributions are consistent with an upper atmospheric source for O{sub 3} and South American coastal sources for marine boundary layer (MBL) CO and aerosol, most of which is acidic sulfate in agreement with the dominant pollution source being SO{sub 2} from Cu smelters and power plants. Pollutant layers in the free troposphere (FT) can be a result of emissions to the north in Peru or long range transport from the west. At a given altitude in the FT (up to 3 km), dew point varies by 40 C with dry air descending from the upper atmospheric and moist air having a BL contribution. Ascent of BL air to a cold high altitude results in the condensation and precipitation removal of all but a few percent of BL water along with aerosol that served as CCN. Thus, aerosol volume decreases with dew point in the FT. Aerosol size spectra have a bimodal structure in the MBL and an intermediate diameter unimodal distribution in the FT. Comparing cloud droplet number concentration (CDNC) and pre-cloud aerosol (Dp > 100 nm) gives a linear relation up to a number concentration of {approx}150 cm{sup -3}, followed by a less than proportional increase in CDNC at higher aerosol number concentration. A number balance between below cloud aerosol and cloud droplets indicates that {approx}25% of aerosol in the PCASP size range are interstitial (not activated). One hundred and two constant altitude cloud transects were identified and used to determine properties of interstitial aerosol. One transect is examined in detail as a case study. Approximately 25 to 50% of aerosol with D{sub p} > 110 nm were not activated, the difference between the two

  5. Aerosol concentration and size distribution measured below, in, and above cloud from the DOE G-1 during VOCALS-REx

    NASA Astrophysics Data System (ADS)

    Kleinman, L. I.; Daum, P. H.; Lee, Y.-N.; Lewis, E. R.; Sedlacek, A. J., III; Senum, G. I.; Springston, S. R.; Wang, J.; Hubbe, J.; Jayne, J.; Min, Q.; Yum, S. S.; Allen, G.

    2011-06-01

    During the VOCALS Regional Experiment, the DOE G-1 aircraft was used to sample a varying aerosol environment pertinent to properties of stratocumulus clouds over a longitude band extending 800 km west from the Chilean coast at Arica. Trace gas and aerosol measurements are presented as a function of longitude, altitude, and dew point in this study. Spatial distributions are consistent with an upper atmospheric source for O3 and South American coastal sources for marine boundary layer (MBL) CO and aerosol, most of which is acidic sulfate in agreement with the dominant pollution source being SO2 from Cu smelters and power plants. Pollutant layers in the free troposphere (FT) can be a result of emissions to the north in Peru or long range transport from the west. At a given altitude in the FT (up to 3 km), dew point varies by 40 °C with dry air descending from the upper atmospheric and moist air having a BL contribution. Ascent of BL air to a cold high altitude results in the condensation and precipitation removal of all but a few percent of BL water along with aerosol that served as CCN. Thus, aerosol volume decreases with dew point in the FT. Aerosol size spectra have a bimodal structure in the MBL and an intermediate diameter unimodal distribution in the FT. Comparing cloud droplet number concentration (CDNC) and pre-cloud aerosol (Dp > 100 nm) gives a linear relation up to a number concentration of ~150 cm-3, followed by a less than proportional increase in CDNC at higher aerosol number concentration. A number balance between below cloud aerosol and cloud droplets indicates that ~25 % of aerosol in the PCASP size range are interstitial (not activated). One hundred and two constant altitude cloud transects were identified and used to determine properties of interstitial aerosol. One transect is examined in detail as a case study. Approximately 25 to 50 % of aerosol with Dp > 110 nm were not activated, the difference between the two approaches possibly representing

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

    SciTech Connect

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

    1995-05-01

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

  7. An observational study of night time aerosol concentrations in the lower atmosphere at a tropical coastal station

    NASA Astrophysics Data System (ADS)

    Parameswaran, K.; Rajeev, K.; Sen Gupta, K.

    1997-09-01

    Aerosol number densities in the lower troposphere measured by a bistatic CW lidar are used to study their altitude structure in the nocturnal mixing region and its association with stratified turbulence. In the early night hours the aerosol concentration shows a maximum just above the daytime Thermal Internal Boundary Layer. This maximum disappears in the late night hours. The integrated aerosol content in the first 1 km shows a general decrease during the post-midnight hours. Stratified aerosol layers are observed in the nocturnal mixing region during the post-midnight period. The association between these stratified aerosol layers and the prevailing atmospheric stability condition in this region is studied using the altitude profiles of different meteorological parameters obtained from pilot balloon and tethered balloonsonde observations.

  8. Capstone depleted uranium aerosol biokinetics, concentrations, and doses.

    PubMed

    Guilmette, Raymond A; Miller, Guthrie; Parkhurst, Mary Ann

    2009-03-01

    One of the principal goals of the Capstone Depleted Uranium (DU) Aerosol Study was to quantify and characterize DU aerosols generated inside armored vehicles by perforation with a DU penetrator. This study consequently produced a database in which the DU aerosol source terms were specified both physically and chemically for a variety of penetrator-impact geometries and conditions. These source terms were used to calculate radiation doses and uranium concentrations for various scenarios as part of the Capstone Human Health Risk Assessment (HHRA). This paper describes the scenario-related biokinetics of uranium, and summarizes intakes, chemical concentrations to the organs, and E(50) and HT(50) for organs and tissues based on exposure scenarios for personnel in vehicles at the time of perforation as well as for first responders. For a given exposure scenario (duration time and breathing rates), the range of DU intakes among the target vehicles and shots was not large, about a factor of 10, with the lowest being for a ventilated operational Abrams tank and the highest being for an unventilated Abrams with DU penetrator perforating DU armor. The ranges of committed effective doses were more scenario-dependent than were intakes. For example, the largest range, a factor of 20, was shown for scenario A, a 1 min exposure, whereas, the range was only a factor of two for the first-responder scenario (E). In general, the committed effective doses were found to be in the tens of mSv. The risks ascribed to these doses are discussed separately.

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

    PubMed

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

    2009-09-01

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

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

    NASA Astrophysics Data System (ADS)

    Struthers, H.; Ekman, A. M. L.; Glantz, P.; Iversen, T.; Kirkevåg, A.; Mårtensson, E. M.; Seland, Ø.; Nilsson, E. D.

    2011-04-01

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

  11. Relationships among particle number, surface area, and respirable mass concentrations in automotive engine manufacturing.

    PubMed

    Heitbrink, William A; Evans, Douglas E; Ku, Bon Ki; Maynard, Andrew D; Slavin, Thomas J; Peters, Thomas M

    2009-01-01

    This study investigated the relationships between particle number, surface area, and respirable mass concentration measured simultaneously in a foundry and an automotive engine machining and assembly center. Aerosol concentrations were measured throughout each plant with a condensation particle counter for number concentration, a diffusion charger for active surface area concentration, and an optical particle counter for respirable mass concentration. At selected locations, particle size distributions were characterized with the optical particle counter and an electrical low pressure impactor. Statistical analyses showed that active surface area concentration was correlated with ultrafine particle number concentration and weakly correlated with respirable mass concentration. Correlation between number and active surface area concentration was stronger during winter (R2 = 0.6 for both plants) than in the summer (R2 = 0.38 and 0.36 for the foundry and engine plant respectively). The stronger correlation in winter was attributed to use of direct-fire gas fired heaters that produced substantial numbers of ultrafine particles with a modal diameter between 0.007 and 0.023 mu m. These correlations support findings obtained through theoretical analysis. Such analysis predicts that active surface area increasingly underestimates geometric surface area with increasing particle size, particularly for particles larger than 100 nm. Thus, a stronger correlation between particle number concentration and active surface area concentration is expected in the presence of high concentrations of ultrafine particles. In general, active surface area concentration may be a concentration metric that is distinct from particle number concentration and respirable mass concentration. For future health effects or toxicological studies involving nano-materials or ultrafine aerosols, this finding needs to be considered, as exposure metrics may influence data interpretation.

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

    NASA Astrophysics Data System (ADS)

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

    2017-01-01

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

  13. Aerosol ion concentration dependence on atmospheric conditions in Chicago

    NASA Astrophysics Data System (ADS)

    Fosco, Tinamarie; Schmeling, Martina

    This study seeks to determine the influence of precursor trace gases and local meteorology, including lake breeze events, on the concentrations of secondary aerosol species in Chicago. For this, two particulate air samples per day were collected onto quartz fiber filters at the Loyola University Chicago Air Station (LUCAS) during the summer months of 2002 and 2003 and subsequently analyzed by ion chromatography for sulfate, nitrate and oxalate. In parallel, mixing ratios of ozone (O 3) and nitrogen oxides (NO and NO 2dbnd NO x) were monitored and weather parameters were recorded. In addition, backward trajectories were obtained to estimate air mass transport to Chicago. Ozone and NO x mixing ratios as well as sulfate, nitrate and oxalate concentrations varied substantially throughout the study, but three situations could be distinguished based on meteorology and chemistry. Case one had the lowest ozone, NO x and ion levels due to wind directions constantly from Lake Michigan. Case two comprised of days showing the highest pollutant levels because of to predominantly southwestern air currents and warm temperatures and case three experienced an air stagnation situation in the morning leading to high NO x mixing ratios and a subsequent lake breeze event. In the last case, elevated ozone mixing ratios and ion concentrations were observed after lake breeze onset indicating pollutant transport.

  14. Particle number concentrations over Europe in 2030: the role of emissions and new particle formation

    NASA Astrophysics Data System (ADS)

    Ahlm, L.; Julin, J.; Fountoukis, C.; Pandis, S. N.; Riipinen, I.

    2013-04-01

    The aerosol particle number concentration is a key parameter when estimating impacts of aerosol particles on climate and human health. We use a three-dimensional chemical transport model with detailed microphysics, PMCAMx-UF, to simulate particle number concentrations over Europe in the year 2030, by applying emission scenarios for trace gases and primary aerosols. The scenarios are based on expected changes in anthropogenic emissions of sulphur dioxide, ammonia, nitrogen oxides, and primary aerosol particles with a diameter less than 2.5 μm (PM2.5) focusing on a photochemically active period. For the baseline scenario, which represents a best estimate of the evolution of anthropogenic emissions in Europe, PMCAMx-UF predicts that the total particle number concentration (Ntot) will decrease by 30-70% between 2008 and 2030. The number concentration of particles larger than 100 nm (N100), a proxy for cloud condensation nuclei (CCN) concentration, is predicted to decrease by 40-70% during the same period. The predicted decrease in Ntot is mainly a result of reduced new particle formation due to the expected reduction in SO2 emissions, whereas the predicted decrease in N100 is a result of both decreasing condensational growth and reduced primary aerosol emissions. For larger emission reductions, PMCAMx-UF predicts reductions of 60-80% in both Ntot and N100 over Europe. Sensitivity tests reveal that a reduction in SO2 emissions is far more efficient than any other emission reduction investigated, in reducing Ntot. For N100, emission reductions of both SO2 and PM2.5 contribute significantly to the reduced concentration, even though SO2 plays the dominant role once more. The impact of SO2 for both new particle formation and growth over Europe may be expected to be somewhat higher during the simulated period with high photochemical activity than during times of the year with less incoming solar radiation. The predicted reductions in both Ntot and N100 between 2008 and 2030

  15. Particle number concentrations over Europe in 2030: the role of emissions and new particle formation

    NASA Astrophysics Data System (ADS)

    Ahlm, L.; Julin, J.; Fountoukis, C.; Pandis, S. N.; Riipinen, I.

    2013-10-01

    The aerosol particle number concentration is a key parameter when estimating impacts of aerosol particles on climate and human health. We use a three-dimensional chemical transport model with detailed microphysics, PMCAMx-UF, to simulate particle number concentrations over Europe in the year 2030, by applying emission scenarios for trace gases and primary aerosols. The scenarios are based on expected changes in anthropogenic emissions of sulfur dioxide, ammonia, nitrogen oxides, and primary aerosol particles with a diameter less than 2.5 μm (PM2.5) focusing on a photochemically active period, and the implications for other seasons are discussed. For the baseline scenario, which represents a best estimate of the evolution of anthropogenic emissions in Europe, PMCAMx-UF predicts that the total particle number concentration (Ntot) will decrease by 30-70% between 2008 and 2030. The number concentration of particles larger than 100 nm (N100), a proxy for cloud condensation nuclei (CCN) concentration, is predicted to decrease by 40-70% during the same period. The predicted decrease in Ntot is mainly a result of reduced new particle formation due to the expected reduction in SO2 emissions, whereas the predicted decrease in N100 is a result of both decreasing condensational growth and reduced primary aerosol emissions. For larger emission reductions, PMCAMx-UF predicts reductions of 60-80% in both Ntot and N100 over Europe. Sensitivity tests reveal that a reduction in SO2 emissions is far more efficient than any other emission reduction investigated, in reducing Ntot. For N100, emission reductions of both SO2 and PM2.5 contribute significantly to the reduced concentration, even though SO2 plays the dominant role once more. The impact of SO2 for both new particle formation and growth over Europe may be expected to be somewhat higher during the simulated period with high photochemical activity than during times of the year with less incoming solar radiation. The predicted

  16. Particle concentrations and number size distributions in the planetary boundary layer derived from airship based measurements

    NASA Astrophysics Data System (ADS)

    Tillmann, Ralf; Zhao, Defeng; Ehn, Mikael; Hofzumahaus, Andreas; Holland, Frank; Rohrer, Franz; Kiendler-Scharr, Astrid; Wahner, Andreas

    2014-05-01

    Atmospheric particles play a key role for regional and global climate due to their direct and indirect radiative forcing effects. The concentration and size of the particles are important variables to these effects. Within the continental planetary boundary layer (PBL) the particle number size distribution is influenced by meteorological parameters, local sinks and sources resulting in variable spatial distributions. However, measurements of particle number size distributions over a broad vertical range of the PBL are rare. The airship ZEPPELIN NT is an ideal platform to measure atmospheric aerosols on a regional scale within an altitude range up to 1000 m. For campaigns in the Netherlands, Northern Italy and South Finland in 2012 and 2013 the airship was deployed with a wide range of instruments, including measurements of different trace gases, short lived radicals, solar radiation, aerosols and meteorological parameters. Flights were carried out at different times of the day to investigate the influence of the diurnal evolution of the PBL on atmospheric trace gases and aerosols. During night and early morning hours the concentration and size distribution of atmospheric particles were found to be strongly influenced by the layered structure of the PBL, i.e. the nocturnal boundary layer and the residual layer. Within the residual layer particle concentrations stay relatively constant as this layer is decoupled from ground sources. The particles persist in the accumulation mode as expected for an aged aerosol. In the nocturnal boundary layer particle concentrations and size are more dynamic with higher concentrations than in the residual layer. A few hours after sunrise, the layered structure of the PBL intermixes. During daytime the PBL is well mixed and a negative concentration gradient with increasing height is observed. Several height profiles at different times of the day and at different locations in Europe were measured. The aerosol measurements will be

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

    NASA Astrophysics Data System (ADS)

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

    2013-12-01

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

  18. Number Size distribution of Atmospheric Submicron Aerosols in Thirteen Sites across China

    NASA Astrophysics Data System (ADS)

    Peng, Jianfei; Hu, Min; Wang, Zhibin; Yue, Dingli

    2013-04-01

    Number concentration and size distribution (15-600nm) of atmospheric submicron aerosols have been measured in thirteen sites across China during several campaigns from 2006 to 2011. All the sampling sites are categorized into four types, including five urban sites, four suburban sites, three regional sites and two cruise measurements along the eastern coast of China. Spatial and temporal variation of aerosols in nucleation mode (with particle diameter between 15 and 25 nm), Aitken mode (with particle diameter between 25 and 90 nm) as well as accumulation mode (with particle diameter between 90 and 600 nm) in all sites are investigated. Particle number concentration in urban and suburban sites are 2-5 times higher than in regional and sites and cruise measurements. Higher concentration of nucleation mode particles as well as more new particle formation events are found in urban and suburban sites than in regional sites and cruise measurements, indicating high formation rates in the urban sites due to anthropogenic emission of new particles formation precursors. Aitken mode particles are abundant in both urban sites and suburban sites, with larger variation in urban sites than in suburban sites. Accumulation mode particles present higher concentration in winter than in summer. Diurnal trend of both Aitken and accumulation mode shows a bimodal pattern, while the pattern of Aitken mode particles is much more obvious in urban sites but can be barely found in cruise measurements. Particle concentration in accumulation mode and Aitken mode have a week correlation, with aerosols in different sites occupying different Aitken/Accumulation region. Log-normal modal fitting treatment are also used on particle size distribution data to provide the modal pattern as well as the aging information. Particle size distribution shows bimodal or trimodal patterns in most cases in urban sites. However, in regional sites and cruise measurements, the unimodal fit can always do a good job

  19. 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

  20. Climate Sensitivities due to Stratocumulus Cloud droplet number concentrations

    NASA Astrophysics Data System (ADS)

    Parkes, Ben; Stevens, Laura; Gadian, Alan; Lathman, John; Blyth, Alan

    2010-05-01

    Four experiments have been carried out using the Met Office Unified Model v6.1 (HadGEM1) to investigate the effects of albedo modification on the climate system as the amount of carbon dioxide in the atmosphere continues to rise. This work is designed to analyse and assess the "cloud whiteneing" method of geoengineering postulated in (Latham, 1990) and expanded upon by (Latham et al., 2008)(Salter et al., 2008) and (Rasch et al., 2009). Consideration will be given to the effect of the cloud modification on rainfall rates and global circulation patterns. Furthermore temperature changes in polar regions are investigated to assess the increase in polar sea ice coverage. The four experiments are a control, one with an increase in carbon dioxide by 1% per year and two potential geoengineering scenarios based on a climate with increasing carbon dioxide. The first geoengineering simulation consists of forcing clouds with a cloud droplet number concentration (CDNC) of N = 375 m-3 over three regions of low lying stratocumulus clouds. These regions are the West coasts of California, Peru and Namibia(Latham et al., 2008). The second geoenginnering simulation is based upon forcing all marine environments with a CDNC of N = 375 m-3. Starting conditions for the experiments were provided by the UK Met Office from the A1B simulation used in the 2007 Intergovernmental Panel on Climate Change report(IPCC, 2007). The geoengineering method proposed relies on the aerosol indirect effect(Twomey, 1977) and the second aerosol indirect(Albrecht, 1989) effects on clouds to increase their brightness and prolong their lifetime. The effects of a change in CDNC on a clean marine stratocumulus cloud can be investigated using data collected from the VOCALs field campaign which took place in the South Eastern Pacific in 2008. radiometry and in cloud data has been collected by several aircraft including the FAAM BAe-146 and the NCAR/NSF C-130(Allen & Abel, 2009). The albedo of the observed region

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

    NASA Astrophysics Data System (ADS)

    Humphries, R. S.; Klekociuk, A. R.; Schofield, R.; Keywood, M.; Ward, J.; Wilson, S. R.

    2015-10-01

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

  2. Ice nucleation in the upper troposphere: Sensitivity to aerosol number density, temperature, and cooling rate

    SciTech Connect

    Jensen, E.J.; Toon, O.B.

    1994-09-01

    We have investigated the processes that control ice crystal nucleation in the upper troposphere using a numerical model. Nucleation of ice resulting from cooling was simulated for a range of aerosol number densities, initial temperatures, and cooling rates. In contrast to observations of stratus clouds, we find that the number of ice crystals that nucleate in cirrus is relatively insensitive to the number of aerosols present. The ice crystal size distribution at the end of the nucleation process is unaffected by the assumed initial aerosol number density. Essentially, nucleation continues until enough ice crystals are present such that their deposition growth rapidly depletes the vapor and shuts off any further nucleation. However, the number of ice crystals nucleated increases rapidly with decreasing initial temperature and increasing cooling rate. This temperature dependence alone could explain the large ice crystal number density observed in very cold tropical cirrus.

  3. The effect of aerosol vertical profiles on satellite-estimated surface particle sulfate concentrations

    SciTech Connect

    Liu, Yang; Wang, Zifeng; Wang, Jun; Ferrare, Richard A.; Newsom, Rob K.; Welton, Ellsworth J.

    2011-02-15

    The aerosol vertical distribution is an important factor in determining the relationship between satellite retrieved aerosol optical depth (AOD) and ground-level fine particle pollution concentrations. We evaluate how aerosol profiles measured by ground-based lidar and simulated by models can help improve the association between AOD retrieved by the Multi-angle Imaging Spectroradiometer (MISR) and fine particle sulfate (SO4) concentrations using matched data at two lidar sites. At the Goddard Space Flight Center (GSFC) site, both lidar and model aerosol profiles marginally improve the association between SO4 concentrations and MISR fractional AODs, as the correlation coefficient between cross-validation (CV) and observed SO4 concentrations changes from 0.87 for the no-scaling model to 0.88 for models scaled with aerosol vertical profiles. At the GSFC site, a large amount of urban aerosols resides in the well-mixed boundary layer so the column fractional AODs are already excellent indicators of ground-level particle pollution. In contrast, at the Atmospheric Radiation Measurement Program (ARM) site with relatively low aerosol loadings, scaling substantially improves model performance. The correlation coefficient between CV and observed SO4 concentrations is increased from 0.58 for the no-scaling model to 0.76 in the GEOS-Chem scaling model, and the model bias is reduced from 17% to 9%. In summary, despite the inaccuracy due to the coarse horizontal resolution and the challenges of simulating turbulent mixing in the boundary layer, GEOS-Chem simulated aerosol profiles can still improve methods for estimating surface aerosol (SO4) mass from satellite-based AODs, particularly in rural areas where aerosols in the free troposphere and any long-range transport of aerosols can significantly contribute to the column AOD.

  4. Source appointment of fine particle number and volume concentration during severe haze pollution in Beijing in January 2013.

    PubMed

    Liu, Zirui; Wang, Yuesi; Hu, Bo; Ji, Dongsheng; Zhang, Junke; Wu, Fangkun; Wan, Xin; Wang, Yonghong

    2016-04-01

    Extreme haze episodes repeatedly shrouded Beijing during the winter of 2012-2013, causing major environmental and health problems. To better understand these extreme events, particle number size distribution (PNSD) and particle chemical composition (PCC) data collected in an intensive winter campaign in an urban site of Beijing were used to investigate the sources of ambient fine particles. Positive matrix factorization (PMF) analysis resolved a total of eight factors: two traffic factors, combustion factors, secondary aerosol, two accumulation mode aerosol factors, road dust, and long-range transported (LRT) dust. Traffic emissions (54%) and combustion aerosol (27%) were found to be the most important sources for particle number concentration, whereas combustion aerosol (33%) and accumulation mode aerosol (37%) dominated particle volume concentrations. Chemical compositions and sources of fine particles changed dynamically in the haze episodes. An enhanced role of secondary inorganic species was observed in the formation of haze pollution. Regional transport played an important role for high particles, contribution of which was on average up to 24-49% during the haze episodes. Secondary aerosols from urban background presented the largest contributions (45%) for the rapid increase of fine particles in the severest haze episode. In addition, the invasion of LRT dust aerosols further elevated the fine particles during the extreme haze episode. Our results showed a clear impact of regional transport on the local air pollution, suggesting the importance of regional-scale emission control measures in the local air quality management of Beijing.

  5. Processes Controlling the Seasonal Cycle of Arctic Aerosol Number and Size Distributions

    NASA Astrophysics Data System (ADS)

    Wentworth, G.; Croft, B.; Martin, R.; Leaitch, W. R.; Tunved, P.; Breider, T. J.; D'Andrea, S.; Pierce, J. R.; Murphy, J. G.; Kodros, J.; Abbatt, J.

    2015-12-01

    Measurements at high-Arctic sites show a strong seasonal cycle in aerosol number and size. The number of aerosols with diameters larger than 20 nm exhibits a maximum in late spring associated with a dominant accumulation mode, and a second maximum in the summer associated with a dominant Aitken mode. Seasonal-mean aerosol effective diameter ranges from about 160 nm in summer to 250 nm in winter. This study interprets these seasonal cycles with the GEOS-Chem-TOMAS global aerosol microphysics model. We find improved agreement with in situ measurements (SMPS) of aerosol size at both Alert, Nunavut, and Mt. Zeppelin, Svalbard following model developments: 1) increase the efficiency of wet scavenging in the Arctic summer and 2) represent coagulation between interstitial aerosols and aerosols activated to form cloud droplets. Our simulations indicate that the dominant summer-time Aitken mode is associated with increased efficiency of wet removal, which limits the number of larger aerosols and promotes local new-aerosol formation. We also find an important role of interstitial coagulation in clouds in the Arctic, which limits the number of Aitken-mode aerosols in the non-summer seasons when direct wet removal of these aerosols is inefficient. The summertime Arctic atmosphere is particularly pristine and strongly influenced by natural regional emissions which have poorly understood climate impacts. Especially influenced are the climatic roles of atmospheric particles and clouds. Here we present evidence that ammonia (NH3) emissions from migratory-seabird guano (dung) are the primary contributor to summertime free ammonia levels recently measured in the Canadian Arctic atmosphere. These findings suggest that ammonia from seabird guano is a key factor contributing to bursts of new-particle formation, which are observed every summer in the near-surface atmosphere at Alert, Canada. Chemical transport model simulations show that these newly formed particles can grow by vapour

  6. A comparison of secondary organic aerosol (SOA) yields and composition from ozonolysis of monoterpenes at varying concentrations of NO2

    NASA Astrophysics Data System (ADS)

    Draper, D. C.; Farmer, D. K.; Desyaterik, Y.; Fry, J. L.

    2015-05-01

    The effect of NO2 on secondary organic aerosol (SOA) formation from ozonolysis of α-pinene, β-pinene, Δ3-carene, and limonene was investigated using a dark flow-through reaction chamber. SOA mass yields were calculated for each monoterpene from ozonolysis with varying NO2 concentrations. Kinetics modeling of the first generation gas-phase chemistry suggests that differences in observed aerosol yields for different NO2 concentrations are consistent with NO3 formation and subsequent competition between O3 and NO3 to oxidize each monoterpene. α-pinene was the only monoterpene studied that showed a systematic decrease in both aerosol number concentration and mass concentration with increasing [NO2]. β-pinene and Δ3-carene produced fewer particles at higher [NO2], but both retained moderate mass yields. Limonene exhibited both higher number concentrations and greater mass concentrations at higher [NO2]. SOA from each experiment was collected and analyzed by HPLC-ESI-MS, enabling comparisons between product distributions for each system. In general, the systems influenced by NO3 oxidation contained more high molecular weight products (MW >400 amu), suggesting the importance of oligomerization mechanisms in NO3-initiated SOA formation. α-pinene, which showed anomalously low aerosol mass yields in the presence of NO2, showed no increase in these oligomer peaks, suggesting that lack of oligomer formation is a likely cause of α-pinene's near 0% yields with NO3. Through direct comparisons of mixed-oxidant systems, this work suggests that NO3 is likely to dominate nighttime oxidation pathways in most regions with both biogenic and anthropogenic influences. Therefore, accurately constraining SOA yields from NO3 oxidation, which vary substantially with the VOC precursor, is essential in predicting nighttime aerosol production.

  7. A qualitative comparison of secondary organic aerosol yields and composition from ozonolysis of monoterpenes at varying concentrations of NO2

    NASA Astrophysics Data System (ADS)

    Draper, D. C.; Farmer, D. K.; Desyaterik, Y.; Fry, J. L.

    2015-11-01

    The effect of NO2 on secondary organic aerosol (SOA) formation from ozonolysis of α-pinene, β-pinene, Δ3-carene, and limonene was investigated using a dark flow-through reaction chamber. SOA mass yields were calculated for each monoterpene from ozonolysis with varying NO2 concentrations. Kinetics modeling of the first-generation gas-phase chemistry suggests that differences in observed aerosol yields for different NO2 concentrations are consistent with NO3 formation and subsequent competition between O3 and NO3 to oxidize each monoterpene. α-Pinene was the only monoterpene studied that showed a systematic decrease in both aerosol number concentration and mass concentration with increasing [NO2]. β-Pinene and Δ3-carene produced fewer particles at higher [NO2], but both retained moderate mass yields. Limonene exhibited both higher number concentrations and greater mass concentrations at higher [NO2]. SOA from each experiment was collected and analyzed by HPLC-ESI-MS, enabling comparisons between product distributions for each system. In general, the systems influenced by NO3 oxidation contained more high molecular weight products (MW > 400 amu), suggesting the importance of oligomerization mechanisms in NO3-initiated SOA formation. α-Pinene, which showed anomalously low aerosol mass yields in the presence of NO2, showed no increase in these oligomer peaks, suggesting that lack of oligomer formation is a likely cause of α-pinene's near 0 % yields with NO3. Through direct comparisons of mixed-oxidant systems, this work suggests that NO3 is likely to dominate nighttime oxidation pathways in most regions with both biogenic and anthropogenic influences. Therefore, accurately constraining SOA yields from NO3 oxidation, which vary substantially with the volatile organic compound precursor, is essential in predicting nighttime aerosol production.

  8. On the competition among aerosol number, size and composition in predicting CCN variability: a multi-annual field study in an urbanized desert

    NASA Astrophysics Data System (ADS)

    Crosbie, E.; Youn, J.-S.; Balch, B.; Wonaschütz, A.; Shingler, T.; Wang, Z.; Conant, W. C.; Betterton, E. A.; Sorooshian, A.

    2015-06-01

    A 2-year data set of measured CCN (cloud condensation nuclei) concentrations at 0.2 % supersaturation is combined with aerosol size distribution and aerosol composition data to probe the effects of aerosol number concentrations, size distribution and composition on CCN patterns. Data were collected over a period of 2 years (2012-2014) in central Tucson, Arizona: a significant urban area surrounded by a sparsely populated desert. Average CCN concentrations are typically lowest in spring (233 cm-3), highest in winter (430 cm-3) and have a secondary peak during the North American monsoon season (July to September; 372 cm-3). There is significant variability outside of seasonal patterns, with extreme concentrations (1 and 99 % levels) ranging from 56 to 1945 cm-3 as measured during the winter, the season with highest variability. Modeled CCN concentrations based on fixed chemical composition achieve better closure in winter, with size and number alone able to predict 82 % of the variance in CCN concentration. Changes in aerosol chemical composition are typically aligned with changes in size and aerosol number, such that hygroscopicity can be parameterized even though it is still variable. In summer, models based on fixed chemical composition explain at best only 41 % (pre-monsoon) and 36 % (monsoon) of the variance. This is attributed to the effects of secondary organic aerosol (SOA) production, the competition between new particle formation and condensational growth, the complex interaction of meteorology, regional and local emissions and multi-phase chemistry during the North American monsoon. Chemical composition is found to be an important factor for improving predictability in spring and on longer timescales in winter. Parameterized models typically exhibit improved predictive skill when there are strong relationships between CCN concentrations and the prevailing meteorology and dominant aerosol physicochemical processes, suggesting that similar findings could be

  9. On the competition among aerosol number, size and composition in predicting CCN variability: a multi-annual field study in an urbanized desert

    PubMed Central

    Crosbie, E.; Youn, J.-S.; Balch, B.; Wonaschütz, A.; Shingler, T.; Wang, Z.; Conant, W. C.; Betterton, E. A.; Sorooshian, A.

    2015-01-01

    A 2-year data set of measured CCN (cloud condensation nuclei) concentrations at 0.2 % supersaturation is combined with aerosol size distribution and aerosol composition data to probe the effects of aerosol number concentrations, size distribution and composition on CCN patterns. Data were collected over a period of 2 years (2012–2014) in central Tucson, Arizona: a significant urban area surrounded by a sparsely populated desert. Average CCN concentrations are typically lowest in spring (233 cm−3), highest in winter (430 cm−3) and have a secondary peak during the North American monsoon season (July to September; 372 cm−3). There is significant variability outside of seasonal patterns, with extreme concentrations (1 and 99 % levels) ranging from 56 to 1945 cm−3 as measured during the winter, the season with highest variability. Modeled CCN concentrations based on fixed chemical composition achieve better closure in winter, with size and number alone able to predict 82% of the variance in CCN concentration. Changes in aerosol chemical composition are typically aligned with changes in size and aerosol number, such that hygroscopicity can be parameterized even though it is still variable. In summer, models based on fixed chemical composition explain at best only 41% (pre-monsoon) and 36% (monsoon) of the variance. This is attributed to the effects of secondary organic aerosol (SOA) production, the competition between new particle formation and condensational growth, the complex interaction of meteorology, regional and local emissions and multi-phase chemistry during the North American monsoon. Chemical composition is found to be an important factor for improving predictability in spring and on longer timescales in winter. Parameterized models typically exhibit improved predictive skill when there are strong relationships between CCN concentrations and the prevailing meteorology and dominant aerosol physicochemical processes, suggesting that similar findings

  10. On the competition among aerosol number, size and composition in predicting CCN variability: a multi-annual field study in an urbanized desert.

    PubMed

    Crosbie, E; Youn, J-S; Balch, B; Wonaschütz, A; Shingler, T; Wang, Z; Conant, W C; Betterton, E A; Sorooshian, A

    2015-02-10

    A 2-year data set of measured CCN (cloud condensation nuclei) concentrations at 0.2 % supersaturation is combined with aerosol size distribution and aerosol composition data to probe the effects of aerosol number concentrations, size distribution and composition on CCN patterns. Data were collected over a period of 2 years (2012-2014) in central Tucson, Arizona: a significant urban area surrounded by a sparsely populated desert. Average CCN concentrations are typically lowest in spring (233 cm(-3)), highest in winter (430 cm(-3)) and have a secondary peak during the North American monsoon season (July to September; 372 cm(-3)). There is significant variability outside of seasonal patterns, with extreme concentrations (1 and 99 % levels) ranging from 56 to 1945 cm(-3) as measured during the winter, the season with highest variability. Modeled CCN concentrations based on fixed chemical composition achieve better closure in winter, with size and number alone able to predict 82% of the variance in CCN concentration. Changes in aerosol chemical composition are typically aligned with changes in size and aerosol number, such that hygroscopicity can be parameterized even though it is still variable. In summer, models based on fixed chemical composition explain at best only 41% (pre-monsoon) and 36% (monsoon) of the variance. This is attributed to the effects of secondary organic aerosol (SOA) production, the competition between new particle formation and condensational growth, the complex interaction of meteorology, regional and local emissions and multi-phase chemistry during the North American monsoon. Chemical composition is found to be an important factor for improving predictability in spring and on longer timescales in winter. Parameterized models typically exhibit improved predictive skill when there are strong relationships between CCN concentrations and the prevailing meteorology and dominant aerosol physicochemical processes, suggesting that similar findings

  11. Concentrations and sources of organic carbon aerosols in the free troposphere over North America

    NASA Astrophysics Data System (ADS)

    Heald, Colette L.; Jacob, Daniel J.; Turquety, SolèNe; Hudman, Rynda C.; Weber, Rodney J.; Sullivan, Amy P.; Peltier, Richard E.; Atlas, Eliot L.; de Gouw, Joost A.; Warneke, Carsten; Holloway, John S.; Neuman, J. Andrew; Flocke, Frank M.; Seinfeld, John H.

    2006-12-01

    Aircraft measurements of water-soluble organic carbon (WSOC) aerosol over NE North America during summer 2004 (ITCT-2K4) are simulated with a global chemical transport model (GEOS-Chem) to test our understanding of the sources of organic carbon (OC) aerosol in the free troposphere (FT). Elevated concentrations were observed in plumes from boreal fires in Alaska and Canada. WSOC aerosol concentrations outside of these plumes average 0.9 ± 0.9 μg C m-3 in the FT (2-6 km). The corresponding model value is 0.7 ± 0.6 μg C m-3, including 42% from biomass burning, 36% from biogenic secondary organic aerosol (SOA), and 22% from anthropogenic emissions. Previous OC aerosol observations over the NW Pacific in spring 2001 (ACE-Asia) averaged 3.3 ± 2.8 μg C m-3 in the FT, compared to a model value of 0.3 ± 0.3 μg C m-3. WSOC aerosol concentrations in the boundary layer (BL) during ITCT-2K4 are consistent with OC aerosol observed at the IMPROVE surface network. The model is low in the boundary layer by 30%, which we attribute to secondary formation at a rate comparable to primary anthropogenic emission. Observed WSOC aerosol concentrations decrease by a factor of 2 from the BL to the FT, as compared to a factor of 10 decrease for sulfate, indicating that most of the WSOC aerosol in the FT originates in situ. Despite reproducing mean observed WSOC concentrations in the FT to within 25%, the model cannot account for the variance in the observations (R = 0.21). Covariance analysis of FT WSOC aerosol with other measured chemical variables suggests an aqueous-phase mechanism for SOA generation involving biogenic precursors.

  12. Calculating Capstone depleted uranium aerosol concentrations from beta activity measurements.

    PubMed

    Szrom, Frances; Falo, Gerald A; Parkhurst, Mary Ann; Whicker, Jeffrey J; Alberth, David P

    2009-03-01

    Beta activity measurements were used as surrogate measurements of uranium mass in aerosol samples collected during the field testing phase of the Capstone Depleted Uranium (DU) Aerosol Study. These aerosol samples generated by the perforation of armored combat vehicles were used to characterize the DU source term for the subsequent Human Health Risk Assessment (HHRA) of Capstone aerosols. Establishing a calibration curve between beta activity measurements and uranium mass measurements is straightforward if the uranium isotopes are in equilibrium with their immediate short-lived, beta-emitting progeny. For DU samples collected during the Capstone study, it was determined that the equilibrium between the uranium isotopes and their immediate short-lived, beta-emitting progeny had been disrupted when penetrators had perforated target vehicles. Adjustments were made to account for the disrupted equilibrium and for wall losses in the aerosol samplers. Values for the equilibrium fraction ranged from 0.16 to 1, and the wall loss correction factors ranged from 1 to 1.92. This paper describes the process used and adjustments necessary to calculate uranium mass from proportional counting measurements.

  13. A balloon-borne aerosol spectrometer for high altitude low aerosol concentration measurements

    SciTech Connect

    Brown, G.S. ); Weiss, R.E. )

    1990-08-01

    Funded by Air Force Wright Aeronautical Laboratory, a new balloon-borne high altitude aerosol spectrometer, for the measurement of cirrus cloud ice crystals, has been developed and successfully flown by Sandia National Laboratories and Radiance Research. This report (1) details the aerosol spectrometer design and construction, (2) discusses data transmission and decoding, (3) presents data collected on three Florida flights in tables and plots. 2 refs., 11 figs., 3 tabs.

  14. Limits of DPUI application associated with the number of particles within actinide aerosols.

    PubMed

    Fritsch, P; Raynaud, P; Blanchin, N; Mièle, A

    2007-01-01

    Dose per unit intake (DPUI) of radionuclides is obtained using International Commission on Radiological Protection (ICRP) models. After inhalation exposure, the first model calculates the fraction of activity deposited within the different regions of the respiratory tract, assuming that the aerosol contains an infinite number of particles. Using default parameters for workers, an exposure to one annual limit of intake (ALI) corresponds to an aerosol of 239PuO2 containing approximately 1 x 10(6) particles. To reach such an exposure, very low particle number might be involved especially for compounds having a high specific activity. This study provides examples of exposures to actinide aerosols for which the number of particles is too low for a standard application of the ICRP model. These examples, which involve physical studies of aerosols collected at the workplace and interpretation of bioassay data, show that the number of particles of the aerosol can be the main limit for the application of DPUI after inhalation exposure.

  15. Observations of high droplet number concentrations in Southern Ocean boundary layer clouds

    NASA Astrophysics Data System (ADS)

    Chubb, T.; Huang, Y.; Jensen, J.; Campos, T.; Siems, S.; Manton, M.

    2015-09-01

    Data from the standard cloud physics payload during the NSF/NCAR High-performance Instrumented Airborne Platform for Environmental Research (HIAPER) Pole-to-Pole Observations (HIPPO) campaigns provide a snapshot of unusual wintertime microphysical conditions in the boundary layer over the Southern Ocean. On 29 June 2011, the HIAPER sampled the boundary layer in a region of pre-frontal warm air advection between 58 and 48° S to the south of Tasmania. Cloud droplet number concentrations were consistent with climatological values in the northernmost profiles but were exceptionally high for wintertime in the Southern Ocean at 100-200 cm-3 in the southernmost profiles. Sub-micron (0.06aerosol concentrations for the southern profiles were up to 400 cm-3. Analysis of back trajectories and atmospheric chemistry observations revealed that while conditions in the troposphere were more typical of a clean remote ocean airmass, there was some evidence of continental or anthropogenic influence. However, the hypothesis of long range transport of continental aerosol fails to explain the magnitude of the aerosol and cloud droplet concentration in the boundary layer. Instead, the gale force surface winds in this case (wind speed at 167 m above sea level was >25 m s-1) were most likely responsible for production of sea spray aerosol which influenced the microphysical properties of the boundary layer clouds. The smaller size and higher number concentration of cloud droplets is inferred to increase the albedo of these clouds, and these conditions occur regularly, and are expected to increase in frequency, over windy parts of the Southern Ocean.

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

    SciTech Connect

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

    2007-06-25

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

  17. Middle East measurements of concentration and size distribution of aerosol particles for coastal zones

    NASA Astrophysics Data System (ADS)

    Bendersky, Sergey; Kopeika, Norman S.; Blaunstein, Natan S.

    2005-10-01

    Recently, an extension of the Navy Aerosol Model (NAM) was proposed based on analysis of an extensive series of measurements at the Irish Atlantic Coast and at the French Mediterranean Coast. We confirm the relevance of that work for the distant eastern Meditteranean and extend several coefficients of that coastal model, proposed by Piazzola et al. for the Meditteranean Coast (a form of the Navy Aerosol Model), to midland Middle East coastal environments. This analysis is based on data collected at three different Middle East coastal areas: the Negev Desert (Eilat) Red Sea Coast, the Sea of Galilee (Tiberias) Coast, and the Mediterranean (Haifa) Coast. Aerosol size distributions are compared with those obtained through measurements carried out over the Atlantic, Pacific, and Indian Ocean Coasts, and Mediterranean, and Baltic Seas Coasts. An analysis of these different results allows better understanding of the similarities and differences between different coastal lake, sea, and open ocean zones. It is shown that in the coastal regions in Israel, compared to open ocean and other sea zones, larger differences in aerosol particle concentration are observed. The aerosol particle concentrations and their dependences on wind speed for these coastal zones are analyzed and discussed. We propose to classify the aerosol distribution models to either: 1. a coastal model with marine aerosol domination; 2. a coastal model with continental aerosol domination (referred to as midland coast in this work); or 3. a coastal model with balanced marine and continental conditions.

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

    NASA Astrophysics Data System (ADS)

    Hansen, A. M. K.; Kristensen, K.; Nguyen, Q. T.; Zare, A.; Cozzi, F.; Nøjgaard, J. K.; Skov, H.; Brandt, J.; Christensen, J. H.; Ström, J.; Tunved, P.; Krejci, R.; Glasius, M.

    2014-08-01

    Sources, composition and occurrence of secondary organic aerosols in the Arctic were investigated at Zeppelin Mountain, Svalbard, and Station Nord, northeastern Greenland, during the full annual cycle of 2008 and 2010, respectively. Speciation of organic acids, organosulfates and nitrooxy organosulfates - from both anthropogenic and biogenic precursors were in focus. A total of 11 organic acids (terpenylic acid, benzoic acid, phthalic acid, pinic acid, suberic acid, azelaic acid, adipic acid, pimelic acid, pinonic acid, diaterpenylic acid acetate and 3-methyl-1,2,3-butanetricarboxylic acid), 12 organosulfates and 1 nitrooxy organosulfate were identified in aerosol samples from the two sites using a high-performance liquid chromatograph (HPLC) coupled to a quadrupole Time-of-Flight mass spectrometer. At Station Nord, compound concentrations followed a distinct annual pattern, where high mean concentrations of organosulfates (47 ± 14 ng m-3) and organic acids (11.5 ± 4 ng m-3) were observed in January, February and March, contrary to considerably lower mean concentrations of organosulfates (2 ± 3 ng m-3) and organic acids (2.2 ± 1 ng m-3) observed during the rest of the year. At Zeppelin Mountain, organosulfate and organic acid concentrations remained relatively constant during most of the year at a mean concentration of 15 ± 4 ng m-3 and 3.9 ± 1 ng m-3, respectively. However during four weeks of spring, remarkably higher concentrations of total organosulfates (23-36 ng m-3) and total organic acids (7-10 ng m-3) were observed. Elevated organosulfate and organic acid concentrations coincided with the Arctic haze period at both stations, where northern Eurasia was identified as the main source region. Air mass transport from northern Eurasia to Zeppelin Mountain was associated with a 100% increase in the number of detected organosulfate species compared with periods of air mass transport from the Arctic Ocean, Scandinavia and Greenland. The results from this

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

    PubMed

    Jeong, Jaein I; Park, Rokjin J

    2017-02-01

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

  20. Measured and modelled cloud condensation nuclei (CCN) concentration in São Paulo, Brazil: the importance of aerosol size-resolved chemical composition on CCNhack concentration prediction

    NASA Astrophysics Data System (ADS)

    Almeida, G. P.; Brito, J.; Morales, C. A.; Andrade, M. F.; Artaxo, P.

    2014-07-01

    Measurements of cloud condensation nuclei (CCN), aerosol size distribution and non-refractory chemical composition were performed from 16 to 31 October 2012 in the São Paulo Metropolitan Area (SPMA), Brazil. CCN measurements were performed at 0.23, 0.45, 0.68, 0.90 and 1.13% water supersaturation and were subsequently compared with the Köhler theory, considering the chemical composition. Real-time chemical composition has been obtained by deploying, for the first time in the SPMA, an aerosol chemical ionization monitor (ACSM). CCN closure analyses were performed considering internal mixtures. Average aerosol composition during the studied period yielded (arithmetic mean~± standard deviation) 4.81 ± 3.05, 3.26 ± 2.10, 0.30 ± 0.27, 0.52 ± 0.32, 0.37 ± 0.21 and 0.04 ± 0.04 μg m-3 for organics, BC, NH4, SO4, NO3 and Cl, respectively. Particle number concentration was 12 813 ± 5350 cm-3, with a dominant nucleation mode. CCN concentrations were on average 1090 ± 328 and 3570 ± 1695 cm-3 at SS = 0.23% and SS = 1.13%, respectively. Results show an increase in aerosol hygroscopicity in the afternoon as a result of aerosol photochemical processing, leading to an enhancement of both organic and inorganic secondary aerosols in the atmosphere, as well as an increase in aerosol average diameter. Considering the bulk composition alone, observed CCN concentrations were substantially overpredicted when compared with the Köhler theory (44.1 ± 47.9% at 0.23% supersaturation and 91.4 ± 40.3% at 1.13% supersaturation). Overall, the impact of composition on the calculated CCN concentration (NCCN) decreases with decreasing supersaturation, partially because using bulk composition introduces less bias for large diameters and lower critical supersaturations, defined as the supersaturation at which the cloud droplet activation will take place. Results suggest that the consideration of only inorganic fraction improves the calculated NCCN. Introducing a size-dependent chemical

  1. On the concentration and size distribution of sub-micron aerosol in the Galápagos Islands

    NASA Astrophysics Data System (ADS)

    Sorribas, M.; Gómez Martín, J. C.; Hay, T. D.; Mahajan, A. S.; Cuevas, C. A.; Agama Reyes, M. V.; Paredes Mora, F.; Gil-Ojeda, M.; Saiz-Lopez, A.

    2015-12-01

    During the CHARLEX campaign in the Galápagos Islands, a Scanning Particle Mobility Sizer was deployed on San Cristobal Island in July-August 2011 to carry out size-resolved measurements of the concentration of submicron aerosols. To our knowledge these are the first measurements of aerosol concentrations in this unique environment. The particles with marine origin displayed a tri-modal number size distribution with peak diameters of 0.016 μm, 0.050 μm and 0.174 μm and a cloud-processed intermodal minimum at 0.093 μm. The mean total aerosol number concentration for the marine contribution was 470 ± 160 cm-3. A low particle concentration of 70 ± 50 cm-3 for the nucleation size range was measured, but no evidence of new particle production in the atmospheric marine boundary layer (MBL) was observed. The concentration of the Aitken size mode was found to be related to aerosol entrainment from the free troposphere off the coast of Chile followed by transport within the MBL to the Galápagos Islands. Cloud processing may activate the particles in the Aitken size range, growing through 'in-cloud' sulphate production and increasing the particle concentration in the accumulation size range. The 0.093 μm cloud processed minima suggests that the critical supersaturation at which the particle is activated to a cloud droplet is in the 0.14-0.21% range. The daytime marine particle background concentration was influenced by human activity around the sampling site, as well as by new particle formation triggered by biogenic emissions from the vegetation cover of the island's semiarid lowlands. Effective CCN formation may play a role in the formation and properties of the stratus clouds, which permanently cover the top of the windward side of the islands and establish one of their characteristic climatic bands.

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

    NASA Astrophysics Data System (ADS)

    Hansen, A. M. K.; Kristensen, K.; Nguyen, Q. T.; Zare, A.; Cozzi, F.; Nøjgaard, J. K.; Skov, H.; Brandt, J.; Christensen, J. H.; Ström, J.; Tunved, P.; Krejci, R.; Glasius, M.

    2014-02-01

    , organosulfate and organic acid concentrations remained relatively constant during most of the year at amean concentration of 15 (±4) ng m-3 (accounting for 4 (±1)% of total organic matter) and 3.9 (±1) ng m-3 (accounting for 1.1 (±0.1)% of total organic matter) respectively. However during four weeks of spring remarkably higher concentrations of total organosulfates (23-36 ng m-3) and total organic acids (7-10 ng m-3) were observed. The periods of observed elevated organosulfate and organic acid concentration at Station Nord and at Zeppelin Mountain coincided with the Arctic Haze period. Furthermore, backwards air mass trajectories indicated northern Eurasia as the main source region of the Arctic haze aerosols at both sites. Periods with air mass transport from Russia to Zeppelin Mountain were associated with a doubled number of detected organosulfate species compared with periods of air mass transport from the Arctic Ocean, Scandinavia and Greenland. Our analysis showed the presence of organosulfates and organic acids of both biogenic and anthropogenic origin throughout the year at both Arctic sites. As the formation of organosulfates binds inorganic sulfate, their presence may possibly affect the formation and lifetime of clouds in the Arctic atmosphere.

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

    NASA Astrophysics Data System (ADS)

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

    2016-04-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2017-02-01

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

  5. Effect of stratospheric aerosols on direct sunlight and implications for concentrating solar power.

    PubMed

    Murphy, Daniel M

    2009-04-15

    Light scattering calculations and data show that stratospheric aerosols reduce direct sunlight by about 4 W for every watt reflected to outer space. The balance becomes diffuse sunlight. One consequence of deliberate enhancement of the stratospheric aerosol layer would be a significant reduction in the efficiency of solar power generation systems using parabolic or other concentrating optics. There also would be a reduction in the effectiveness of passive solar design.

  6. The Role of Atmospheric Aerosol Concentration on Deep Convective Precipitation: Cloud-resolving Model Simulations

    NASA Technical Reports Server (NTRS)

    Tao, W.-K.; Li, X.; Khain, A.; Mastsui, T.; Lang, S.; Simpson, J.

    2007-01-01

    Aerosols and especially their effect on clouds are one of the key components of the climate system and the hydrological cycle [Ramanathan et al., 20011. Yet, the aerosol effect on clouds remains largely unknown and the processes involved not well understood. A recent report published by the National Academy of Science states "The greatest uncertainty about the aerosol climate forcing - indeed, the largest of all the uncertainties about global climate forcing - is probably the indirect effect of aerosols on clouds NRC [2001]." The aerosol effect on clouds is often categorized into the traditional "first indirect (i.e., Twomey)" effect on the cloud droplet sizes for a constant liquid water path and the "semi-direct" effect on cloud coverage. The aerosol effect on precipitation processes, also known as the second type of aerosol indirect effect, is even more complex, especially for mixed-phase convective clouds. ln this paper, a cloud-resolving model (CRM) with detailed spectral-bin microphysics was used to examine the effect of aerosols on three different deep convective cloud systems that developed in different geographic locations: South Florida, Oklahoma and the Central Pacific. In all three cases, rain reaches the ground earlier for the low CCN (clean) case. Rain suppression is also evident in all three cases with high CCN (dirty) case. However, this suppression only occurs during the first hour of the simulations. During the mature stages of the simulations, the effects of increasing aerosol concentration range from rain suppression in the Oklahoma case, to almost no effect in the Florida case, to rain enhancement in the Pacific case. These results show the complexity of aerosol interactions with convection.

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

    NASA Astrophysics Data System (ADS)

    Kubicki, Marek; Odzimek, Anna; Neska, Mariusz

    2016-09-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2017-01-01

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

  9. What controls the low ice number concentration in the upper troposphere?

    NASA Astrophysics Data System (ADS)

    Zhou, C.; Penner, J. E.; Lin, G.; Liu, X.; Wang, M.

    2015-12-01

    Cirrus clouds in the tropical tropopause play a key role in regulating the moisture entering the stratosphere through their dehydrating effect. Low ice number concentrations (< 200 L-1) and high supersaturations (150-160 %) have been observed in these clouds. Different mechanisms have been proposed to explain these low ice number concentrations, including the inhibition of homogeneous freezing by the deposition of water vapour onto pre-existing ice crystals, heterogeneous ice formation on glassy organic aerosol ice nuclei (IN), and limiting the formation of ice number from high frequency gravity waves. In this study, we examined the effect from three different representations of updraft velocities, the effect from pre-existing ice crystals, the effect from different water vapour deposition coefficients (α = 0.1 or 1), and the effect of 0.1 % of the total secondary organic aerosol (SOA) particles acting as IN. Model simulated ice crystal numbers are compared against an aircraft observational dataset. Including the effect from water vapour deposition on pre-existing ice particles can effectively reduce simulated in-cloud ice number concentrations for all model set-ups. A larger water vapour deposition coefficient (α = 1) can also efficiently reduce ice number concentrations at temperatures below 205 K but less so at higher temperatures. SOA acting as IN are most effective at reducing ice number concentrations when the effective updraft velocities are moderate (∼ 0.05-0.2 m s-1). However, the effects of including SOA as IN and using (α = 1) are diminished when the effect from pre-existing ice is included. When a grid resolved large-scale updraft velocity (< 0.1 m s-1) is used, the ice nucleation parameterization with homogeneous freezing only or with both homogeneous freezing and heterogeneous nucleation is able to generate low ice number concentrations in good agreement with observations for temperatures below 205 K as long as the pre-existing ice effect is

  10. What controls the low ice number concentration in the upper troposphere?

    NASA Astrophysics Data System (ADS)

    Zhou, Cheng; Penner, Joyce E.; Lin, Guangxing; Liu, Xiaohong; Wang, Minghuai

    2016-10-01

    Cirrus clouds in the tropical tropopause play a key role in regulating the moisture entering the stratosphere through their dehydrating effect. Low ice number concentrations ( < 200 L-1) and high supersaturations (150-160 %) have been observed in these clouds. Different mechanisms have been proposed to explain these low ice number concentrations, including the inhibition of homogeneous freezing by the deposition of water vapour onto pre-existing ice crystals, heterogeneous ice formation on glassy organic aerosol ice nuclei (IN), and limiting the formation of ice number from high-frequency gravity waves. In this study, we examined the effect from three different representations of updraft velocities, the effect from pre-existing ice crystals, the effect from different water vapour deposition coefficients (α = 0.1 or 1), and the effect of 0.1 % of the total secondary organic aerosol (SOA) particles acting as IN. Model-simulated ice crystal numbers are compared against an aircraft observational dataset.Including the effect from water vapour deposition on pre-existing ice particles can effectively reduce simulated in-cloud ice number concentrations for all model setups. A larger water vapour deposition coefficient (α = 1) can also efficiently reduce ice number concentrations at temperatures below 205 K, but less so at higher temperatures. SOA acting as IN is most effective at reducing ice number concentrations when the effective updraft velocities are moderate ( ˜ 0.05-0.2 m s-1). However, the effects of including SOA as IN and using (α = 1) are diminished when the effect from pre-existing ice is included.When a grid-resolved large-scale updraft velocity ( < 0.1 m s-1) is used, the ice nucleation parameterization with homogeneous freezing only or with both homogeneous freezing and heterogeneous nucleation is able to generate low ice number concentrations in good agreement with observations for temperatures below 205 K as long as the pre-existing ice effect is

  11. 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 ...

  12. Emission controls versus meteorological conditions in determining aerosol concentrations in Beijing during the 2008 Olympic Games

    NASA Astrophysics Data System (ADS)

    Gao, Y.; Liu, X.; Zhao, C.; Zhang, M.; Wang, Y.

    2011-06-01

    A series of emission control measures were undertaken in Beijing and the adjacent provinces in China during the 2008 Beijing Olympic Games on 8-24 August 2008. This provides a unique opportunity for investigating the effectiveness of emission controls on air pollution in Beijing. We conducted a series of numerical experiments over East Asia for the period of July to September 2008 using a coupled meteorology-chemistry model (WRF-Chem). Model can generally reproduce the observed variation of aerosol concentrations. Consistent with observations, modeled concentrations of aerosol species (sulfate, nitrate, ammonium, black carbon, organic carbon, total particulate matter) in Beijing were decreased by 30-50 % during the Olympic period compared to the other periods in July and August in 2008 and the same period in 2007. Model results indicate that emission controls were effective in reducing the aerosol concentrations by comparing simulations with and without emission controls. However, our analysis suggests that meteorological conditions (e.g., wind direction and precipitation) are at least as important as emission controls in producing the low aerosol concentrations appearing during the Olympic period. Transport from the regions surrounding Beijing determines the temporal variation of aerosol concentrations in Beijing. Based on the budget analysis, we suggest that to improve the air quality over Beijing, emission control strategy should focus on the regional scale instead of the local scale.

  13. Emission controls versus meteorological conditions in determining aerosol concentrations in Beijing during the 2008 Olympic Games

    NASA Astrophysics Data System (ADS)

    Gao, Y.; Liu, X.; Zhao, C.; Zhang, M.

    2011-12-01

    A series of emission control measures were undertaken in Beijing and the adjacent provinces in China during the 2008 Beijing Olympic Games on 8-24 August 2008. This provides a unique opportunity for investigating the effectiveness of emission controls on air pollution in Beijing. We conducted a series of numerical experiments over East Asia for the period of July to September 2008 using a coupled meteorology-chemistry model (WRF-Chem). Model can generally reproduce the observed variation of aerosol concentrations. Consistent with observations, modeled concentrations of aerosol species (sulfate, nitrate, ammonium, black carbon, organic carbon, total particulate matter) in Beijing were decreased by 30-50% during the Olympic period compared to the other periods in July and August in 2008 and the same period in 2007. Model results indicate that emission controls were effective in reducing the aerosol concentrations by comparing simulations with and without emission controls. In addition to emission controls, our analysis suggests that meteorological conditions (e.g. wind direction and precipitation) were also important in producing the low aerosol concentrations appearing during the Olympic period. Transport from the regions surrounding Beijing determined the daily variation of aerosol concentrations in Beijing. Based on the budget analysis, we suggest that to improve the air quality over Beijing, emission control strategy should focus on the regional scale instead of the local scale.

  14. Emission Controls Versus Meteorological Conditions in Determining Aerosol Concentrations in Beijing during the 2008 Olympic Games

    SciTech Connect

    Gao, Yi; Liu, Xiaohong; Zhao, Chun; Zhang, Meigen

    2011-12-12

    A series of emission control measures were undertaken in Beijing and the adjacent provinces in China during the 2008 Beijing Olympic Games on August 8th-24th, 2008. This provides a unique opportunity for investigating the effectiveness of emission controls on air pollution in Beijing. We conducted a series of numerical experiments over East Asia for the period of July to September 2008 using a coupled meteorology-chemistry model (WRF-Chem). Model can generally reproduce the observed variation of aerosol concentrations. Consistent with observations, modeled concentrations of aerosol species (sulfate, nitrate, ammonium, black carbon, organic carbon, total particulate matter) in Beijing were decreased by 30-50% during the Olympic period compared to the other periods in July and August in 2008 and the same period in 2007. Model results indicate that emission controls were effective in reducing the aerosol concentrations by comparing simulations with and without emission controls. However, our analysis suggests that meteorological conditions (e.g., wind direction and precipitation) are at least as important as emission controls in producing the low aerosol concentrations appearing during the Olympic period. Transport from the regions surrounding Beijing determines the temporal variation of aerosol concentrations in Beijing. Based on the budget analysis, we suggest that emission control strategy should focus on the regional scale instead of the local scale to improve the air quality over Beijing.

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

    NASA Astrophysics Data System (ADS)

    Shi, Chong; Nakajima, Teruyuki; Hashimoto, Makiko

    2016-12-01

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

  16. Spatial variability of carbonaceous aerosol concentrations in East and West Jerusalem.

    PubMed

    von Schneidemesser, Erika; Zhou, Iiabin; Stone, Elizabeth A; Schauer, James I; Shpund, Jacob; Brenner, Shmuel; Qasrawi, Radwan; Abdeen, Ziad; Sarnat, Jeremy A

    2010-03-15

    Carbonaceous aerosol concentrations and sources were compared during a year long study at two sites in East and West Jerusalem that were separated by a distance of approximately 4 km. One in six day 24-h PM(2.5) elemental and organic carbon concentrations were measured, along with monthly average concentrations of particle-phase organic compound tracers for primary and secondary organic aerosol sources.Tracer compounds were used in a chemical mass balance ICMB) model to determine primary and secondary source contributions to organic carbon. The East Jerusalem sampling site at Al Quds University experienced higher concentrations of organic carbon (OC) and elemental carbon (EC) compared to the West Jerusalem site at Hebrew University. The annual average concentrations of OC and EC at the East Jerusalem site were 5.20 and 2.19 μg m(-3), respectively, and at the West Jerusalem site were 4.03 and 1.14 μg m(-3), respectively. Concentrations and trends of secondary organic aerosol and vegetative detritus were similar at both sites, but large differences were observed in the concentrations of organic aerosol from fossil fuel combustion and biomass burning, which was the cause of the large differences in OC and EC concentrations observed at the two sites.

  17. Number of core samples: Mean concentrations and confidence intervals

    SciTech Connect

    Jensen, L.; Cromar, R.D.; Wilmarth, S.R.; Heasler, P.G.

    1995-01-24

    This document provides estimates of how well the mean concentration of analytes are known as a function of the number of core samples, composite samples, and replicate analyses. The estimates are based upon core composite data from nine recently sampled single-shell tanks. The results can be used when determining the number of core samples needed to ``characterize`` the waste from similar single-shell tanks. A standard way of expressing uncertainty in the estimate of a mean is with a 95% confidence interval (CI). The authors investigate how the width of a 95% CI on the mean concentration decreases as the number of observations increase. Specifically, the tables and figures show how the relative half-width (RHW) of a 95% CI decreases as the number of core samples increases. The RHW of a CI is a unit-less measure of uncertainty. The general conclusions are as follows: (1) the RHW decreases dramatically as the number of core samples is increased, the decrease is much smaller when the number of composited samples or the number of replicate analyses are increase; (2) if the mean concentration of an analyte needs to be estimated with a small RHW, then a large number of core samples is required. The estimated number of core samples given in the tables and figures were determined by specifying different sizes of the RHW. Four nominal sizes were examined: 10%, 25%, 50%, and 100% of the observed mean concentration. For a majority of analytes the number of core samples required to achieve an accuracy within 10% of the mean concentration is extremely large. In many cases, however, two or three core samples is sufficient to achieve a RHW of approximately 50 to 100%. Because many of the analytes in the data have small concentrations, this level of accuracy may be satisfactory for some applications.

  18. In Situ Measurements of Aerosol Mass Concentration and Spectral Absorption in Xianghe, SE of Beijing, China

    NASA Astrophysics Data System (ADS)

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

    2005-12-01

    China's rapid industrialization over the last few decades has affected air quality in many regions of China, and even the regional climate. As a part of the EAST-AIRE (East Asian Study of Tropospheric Aerosols: an International Regional Experiment) study, Nuclepore filters were collected in two size ranges (PM10 and PM2.5) at 12 hour intervals since January 2005 at Xianghe, about 70 km southeast of Beijing. Each filter was analyzed for mass concentration, aerosol scattering and absorption efficiencies. Mass concentrations during the winter months (January-March) ranged from 9 to 459 μg/m3 in the coarse mode with an average concentration of 122 μg/m3, and from 11 to 203 μg/m3 in the fine mode with an average concentration of 45 μg/m3. While some of the extreme values are likely linked to local emissions, regional air pollution episodes also played important roles. Absorption efficiency measurements at 550 nm show very high values compared to measurements performed in the United States during the CLAMS experiment. The spectral mass absorption efficiency was measured from 350 to 2500 nm and shows large differences between the absorption properties of soil dust, black carbon, and organic aerosols. The strong spectral differences observed can be related to differences in refractive indices from the several collected species and particle size effects. The absorption properties from aerosols measured in China show large absorption efficiencies, compared to aerosols measured in the US, possibly linked to different technology practices used in these countries. For organic plus black carbon aerosols, where the refractive index seems to be relatively constant, the absorption efficiency spectral dependence for fine mode aerosols falls between 1/λ and 1/λ2. The coarse mode absorption shows much less spectral dependence.

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

    PubMed

    Diwakar, Prasoon K; Kulkarni, Pramod

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

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

    PubMed Central

    Diwakar, Prasoon K.

    2015-01-01

    A coaxial microelectrode system has been used to collect and analyse the elemental composition of aerosol particles in near real-time using spark emission spectroscopy. The technique involves focused electrostatic deposition of charged aerosol particles onto the flat tip of a microelectrode, followed by introduction of spark discharge. A pulsed spark discharge was generated across the electrodes with input energy ranging from 50 to 300 mJ per pulse, resulting in the formation of controlled pulsed plasma. The particulate matter on the cathode tip is ablated and atomized by the spark plasma, resulting in atomic emissions which are subsequently recorded using a broadband optical spectrometer for element identification and quantification. The plasma characteristics were found to be very consistent and reproducible even after several thousands of spark discharges using the same electrode system. The spark plasma was characterized by measuring the excitation temperature (~7000 to 10 000 K), electron density (~1016 cm−3), and evolution of spectral responses as a function of time. The system was calibrated using particles containing Pb, Si, Na and Cr. Absolute mass detection limits in the range 11 pg to 1.75 ng were obtained. Repeatability of spectral measurements varied from 2 to 15%. The technique offers key advantages over similar microplasma-based techniques such as laser-induced breakdown spectroscopy, as: (i) it does not require any laser beam optics and eliminates any need for beam alignment, (ii) pulse energy from dc power supply in SIBS system can be much higher compared to that from laser source of the same physical size, and (iii) it is quite conducive to compact, field-portable instrumentation. PMID:26491209

  1. Aerosol effects on ozone concentrations in Beijing: a model sensitivity study.

    PubMed

    Xu, Jun; Zhang, Yuanhang; Zheng, Shaoqing; He, Youjiang

    2012-01-01

    Most previous O3 simulations were based only on gaseous phase photochemistry. However, some aerosol-related processes, namely, heterogeneous reactions occurring on the aerosol surface and photolysis rate alternated by aerosol radiative influence, may affect O3 photochemistry under high aerosol loads. A three-dimensional air quality model, Models-3/Community Multi-scale Air Quality-Model of Aerosol Dynamics, Reaction, Ionization, and Dissolution, was employed to simulate the effects of the above-mentioned processes on O3 formation under typical high O3 episodes in Beijing during summer. Five heterogeneous reactions, i.e., NO2, NO3, N2O5, HO2, and O3, were individually investigated to elucidate their effects on 03 formation. The results showed that the heterogeneous reactions significantly affected O3 formation in the urban plume. NO2 heterogeneous reaction increased O3 to 90 ppb, while HO2 heterogeneous reaction decreased O3 to 33 ppb. In addition, O3 heterogeneous loss decreased O3 to 31 ppb. The effects of NO2, NO3, and N2O5 heterogeneous reactions showed opposite O3 concentration changes between the urban and extra-urban areas because of the response of the reactions to the two types of O3 formation regimes. When the aerosol radiative influence was included, the photolysis rate decreased and O3 decreased significantly to 73 ppb O3. The two aerosol-related processes should be considered in the study of O3 formation because high aerosol concentration is a ubiquitous phenomenon that affects the urban- and regional air quality in China.

  2. Particle number concentration, size distribution and chemical composition during haze and photochemical smog episodes in Shanghai.

    PubMed

    Wang, Xuemei; Chen, Jianmin; Cheng, Tiantao; Zhang, Renyi; Wang, Xinming

    2014-09-01

    The aerosol number concentration and size distribution as well as size-resolved particle chemical composition were measured during haze and photochemical smog episodes in Shanghai in 2009. The number of haze days accounted for 43%, of which 30% was severe (visibility<2km) and moderate (2km≤visibility<3km) haze, mainly distributed in winter and spring. The mean particle number concentration was about 17,000/cm(3) in haze, more than 2 times that in clean days. The greatest increase of particle number concentration was in 0.5-1μm and 1-10μm size fractions during haze events, about 17.78 times and 8.78 times those of clean days. The largest increase of particle number concentration was within 50-100nm and 100-200nm fractions during photochemical smog episodes, about 5.89 times and 4.29 times those of clean days. The particle volume concentration and surface concentration in haze, photochemical smog and clean days were 102, 49, 15μm(3)/cm(3) and 949, 649, 206μm(2)/cm(3), respectively. As haze events got more severe, the number concentration of particles smaller than 50nm decreased, but the particles of 50-200nm and 0.5-1μm increased. The diurnal variation of particle number concentration showed a bimodal pattern in haze days. All soluble ions were increased during haze events, of which NH4(+), SO4(2-) and NO3(-) increased greatly, followed by Na(+), K(+), Ca(2+) and Cl(-). These ions were very different in size-resolved particles during haze and photochemical smog episodes.

  3. Generation and characterization of stable, highly concentrated titanium dioxide nanoparticle aerosols for rodent inhalation studies

    NASA Astrophysics Data System (ADS)

    Kreyling, Wolfgang G.; Biswas, Pratim; Messing, Maria E.; Gibson, Neil; Geiser, Marianne; Wenk, Alexander; Sahu, Manoranjan; Deppert, Knut; Cydzik, Izabela; Wigge, Christoph; Schmid, Otmar; Semmler-Behnke, Manuela

    2011-02-01

    The intensive use of nano-sized titanium dioxide (TiO2) particles in many different applications necessitates studies on their risk assessment as there are still open questions on their safe handling and utilization. For reliable risk assessment, the interaction of TiO2 nanoparticles (NP) with biological systems ideally needs to be investigated using physico-chemically uniform and well-characterized NP. In this article, we describe the reproducible production of TiO2 NP aerosols using spark ignition technology. Because currently no data are available on inhaled NP in the 10-50 nm diameter range, the emphasis was to generate NP as small as 20 nm for inhalation studies in rodents. For anticipated in vivo dosimetry analyses, TiO2 NP were radiolabeled with 48V by proton irradiation of the titanium electrodes of the spark generator. The dissolution rate of the 48V label was about 1% within the first day. The highly concentrated, polydisperse TiO2 NP aerosol (3-6 × 106 cm-3) proved to be constant over several hours in terms of its count median mobility diameter, its geometric standard deviation, and number concentration. Extensive characterization of NP chemical composition, physical structure, morphology, and specific surface area was performed. The originally generated amorphous TiO2 NP were converted into crystalline anatase TiO2 NP by thermal annealing at 950 °C. Both crystalline and amorphous 20-nm TiO2 NP were chain agglomerated/aggregated, consisting of primary particles in the range of 5 nm. Disintegration of the deposited TiO2 NP in lung tissue was not detectable within 24 h.

  4. Aerosol- and updraft-limited regimes of cloud droplet formation: influence of particle number, size and hygroscopicity on the activation of cloud condensation nuclei (CCN)

    NASA Astrophysics Data System (ADS)

    Reutter, P.; Su, H.; Trentmann, J.; Simmel, M.; Rose, D.; Gunthe, S. S.; Wernli, H.; Andreae, M. O.; Pöschl, U.

    2009-09-01

    We have investigated the formation of cloud droplets under pyro-convective conditions using a cloud parcel model with detailed spectral microphysics and with the κ-Köhler model approach for efficient and realistic description of the cloud condensation nucleus (CCN) activity of aerosol particles. Assuming a typical biomass burning aerosol size distribution (accumulation mode centred at 120 nm), we have calculated initial cloud droplet number concentrations (NCD) for a wide range of updraft velocities (w=0.25-20 m s-1) and aerosol particle number concentrations (NCN=200-105 cm-3) at the cloud base. Depending on the ratio between updraft velocity and particle number concentration (w/NCN), we found three distinctly different regimes of CCN activation and cloud droplet formation: (1) An aerosol-limited regime that is characterized by high w/NCN ratios (>≈10-3 m s-1 cm3), high maximum values of water vapour supersaturation (Smax>≈0.5%), and high activated fractions of aerosol particles (NCN/NCN>≈90%). In this regime NCD is directly proportional to NCN and practically independent of w. (2) An updraft-limited regime that is characterized by low w/NCN ratios (<≈10-4 m s-1 cm3), low maximum values of water vapour supersaturation (Smax<≈0.2%), and low activated fractions of aerosol particles (NCD/NCN<≈20%). In this regime NCD is directly proportional to w and practically independent of NCN. (3) An aerosol- and updraft-sensitive regime (transitional regime), which is characterized by parameter values in between the two other regimes and covers most of the conditions relevant for pyro-convection. In this regime NCD depends non-linearly on both NCN and w. In sensitivity studies we have tested the influence of aerosol particle size distribution and hygroscopicity on NCD. Within the range of effective hygroscopicity parameters that is characteristic for continental atmospheric aerosols (κ≈0.05-0.6), we found that NCD depends rather weakly on the actual value of κ

  5. 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.

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

    NASA Astrophysics Data System (ADS)

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

    2015-11-01

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

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

    PubMed

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

    2016-11-17

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

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

    NASA Astrophysics Data System (ADS)

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

    2016-11-01

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

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

    SciTech Connect

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

    2016-10-24

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

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

    DOE PAGES

    Wang, Jian; Krejci, Radovan; Giangrande, Scott; ...

    2016-10-24

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

  11. The dependence of ice microphysics on aerosol concentration in arctic mixed-phase stratus clouds during ISDAC and M-PACE

    SciTech Connect

    Jackson, Robert C.; McFarquhar, Greg; Korolev, Alexei; Earle, Michael; Liu, Peter S.; Lawson, R. P.; Brooks, Sarah D.; Wolde, Mengistu; Laskin, Alexander; Freer, Matthew

    2012-08-14

    Cloud and aerosol data acquired by the National Research Council of Canada (NRC) Convair-580 aircraft in, above, and below single-layer arctic stratocumulus cloud during the Indirect and Semi-Direct Aerosol Campaign (ISDAC) in April 2008 were used to test three aerosol indirect effects hypothesized to act in mixed-phase clouds: the riming indirect effect, the glaciation indirect effect, and the cold second indirect effect. The data showed a correlation of R= 0.75 between liquid drop number concentration, Nliq, inside cloud and ambient aerosol number concentration NPCASP below cloud. This, combined with increasing liquid water content LWC with height above cloud base and the nearly constant profile of Nliq, suggested that liquid drops were nucleated from aerosol at cloud base. No strong evidence of a riming indirect effect was observed, but a strong correlation of R = 0.69 between ice crystal number concentration Ni and NPCASP above cloud was noted. Increases in ice nuclei (IN) concentration with NPCASP above cloud combined with the subadiabatic LWC profiles suggest possible mixing of IN from cloud top consistent with the glaciation indirect effect. The higher Nice and lower effective radius rel for the more polluted ISDAC cases compared to data collected in cleaner single-layer stratocumulus conditions during the Mixed-Phase Arctic Cloud Experiment is consistent with the operation of the cold second indirect effect. However, more data in a wider variety of meteorological and surface conditions, with greater variations in aerosol forcing, are required to identify the dominant aerosol forcing mechanisms in mixed-phase arctic clouds.

  12. What Controls the Low Ice Number Concentration in the Upper Tropical Troposphere?

    NASA Astrophysics Data System (ADS)

    Penner, J.; Zhou, C.; Lin, G.; Liu, X.; Wang, M.

    2015-12-01

    Cirrus clouds in the tropical tropopause play a key role in regulating the moisture entering the stratosphere through their dehydrating effect. Low ice number concentrations and high supersaturations were frequently were observed in these clouds. However, low ice number concentrations are inconsistent with cirrus cloud formation based on homogeneous freezing. Different mechanisms have been proposed to explain this discrepancy, including the inhibition of homogeneous freezing by pre-existing ice crystals and/or glassy organic aerosol heterogeneous ice nuclei (IN) and limiting the formation of ice number from high frequency gravity waves. In this study, we examined the effect from three different parameterizations of in-cloud updraft velocities, the effect from pre-existing ice crystals, the effect from different water vapor deposition coefficients (α=0.1 or 1), and the effect from 0.1% of secondary organic aerosol (SOA) acting as glassy heterogeneous ice nuclei (IN) in CAM5. Model simulated ice crystal numbers are compared against an aircraft observational dataset. Using grid resolved large-scale updraft velocity in the ice nucleation parameterization generates ice number concentrations in better agreement with observations for temperatures below 205K while using updraft velocities based on the model-generated turbulence kinetic energy generates ice number concentrations in better agreement with observations for temperatures above 205K. A larger water vapor deposition coefficient (α=1) can efficiently reduce the ice number at temperatures below 205K but less so at higher temperatures. Glassy SOA IN are most effective at reducing the ice number concentrations when the effective in-cloud updraft velocities are moderate (~0.05-0.2 m s-1). Including the removal of water vapor on pre-existing ice can also effectively reduce the ice number and diminish the effects from the additional glassy SOA heterogeneous IN. We also re-evaluate whether IN seeding in cirrus cloud is

  13. Sensitivity of warm-frontal processes to cloud-nucleating aerosol concentrations

    NASA Technical Reports Server (NTRS)

    Igel, Adele L.; Van Den Heever, Susan C.; Naud, Catherine M.; Saleeby, Stephen M.; Posselt, Derek J.

    2013-01-01

    An extratropical cyclone that crossed the United States on 9-11 April 2009 was successfully simulated at high resolution (3-km horizontal grid spacing) using the Colorado State University Regional Atmospheric Modeling System. The sensitivity of the associated warm front to increasing pollution levels was then explored by conducting the same experiment with three different background profiles of cloud-nucleating aerosol concentration. To the authors' knowledge, no study has examined the indirect effects of aerosols on warm fronts. The budgets of ice, cloud water, and rain in the simulation with the lowest aerosol concentrations were examined. The ice mass was found to be produced in equal amounts through vapor deposition and riming, and the melting of ice produced approximately 75% of the total rain. Conversion of cloud water to rain accounted for the other 25%. When cloud-nucleating aerosol concentrations were increased, significant changes were seen in the budget terms, but total precipitation remained relatively constant. Vapor deposition onto ice increased, but riming of cloud water decreased such that there was only a small change in the total ice production and hence there was no significant change in melting. These responses can be understood in terms of a buffering effect in which smaller cloud droplets in the mixed-phase region lead to both an enhanced vapor deposition and decreased riming efficiency with increasing aerosol concentrations. Overall, while large changes were seen in the microphysical structure of the frontal cloud, cloud-nucleating aerosols had little impact on the precipitation production of the warm front.

  14. Comparison of sources of submicron particle number concentrations measured at two sites in Rochester, NY.

    PubMed

    Kasumba, John; Hopke, Philip K; Chalupa, David C; Utell, Mark J

    2009-09-01

    Sources contributing to the submicron particles (100-470 nm) measured between January 2002 and December 2007 at two different New York State Department of Environmental Conservation (NYS DEC) sites in Rochester, NY were identified and apportioned using a bilinear receptor model, positive matrix factorization (PMF). Measurements of aerosol size distributions and number concentrations for particles in the size range of 10-500 nm have been made since December 2001 to date in Rochester. The measurements are being made using a scanning mobility particle sizer (SMPS) consisting of a DMA and a CPC (TSI models 3071 and 3010, respectively). From December 2001 to March 2004, particle measurements were made at the NYS DEC site in downtown Rochester, but it was moved to the eastside of Rochester in May 2004. Each measurement period was divided into three seasons i.e., winter (December, January, and February), summer (June, July, and August), and the transitional periods (March, April, May, September, October, and November) so as to avoid experimental uncertainty resulting from too large season-to-season variability in ambient temperature and solar photon intensity that would lead to unstable/non-stationary size distributions. Therefore, the seasons were analyzed independently for possible sources. Ten sources were identified at both sites and these include traffic, nucleation, residential/commercial heating, industrial emissions, secondary nitrate, ozone- rich secondary aerosol, secondary sulfate, regionally transported aerosol, and a mixed source of nucleation and traffic. These results show that the measured total outdoor particle number concentrations in Rochester generally vary with similar temporal patterns, suggesting that the central monitoring site data can be used to estimate outdoor exposure in other parts of the city.

  15. Fire and biofuel annual contributions to aerosol mass concentrations in the United States

    NASA Astrophysics Data System (ADS)

    Park, R. J.; Jacob, D. J.; Logan, J. A.

    2006-12-01

    Fires are a potentially major but poorly quantified factor for air quality degradation in the United States. Although episodic effects are well established, little attention has been paid to the more diffuse, nationwide effects of fires on seasonal and annual aerosol concentrations of relevance for air quality and visibility standards. Effects of biofuel use, both residential and industrial, have also received little attention. We use here correlations with non-soil potassium (ns-K) at the nationwide IMPROVE network of surface sites for 2001- 2004 to estimate total contributions to total carbonaceous (TC) aerosol concentrations from wildfires, prescribed fires, and residential and industrial biofuels. We find that the year-to-year variation of fires largely drives the observed interannual variability in TC. We present estimates of biomass burning contributions to regional aerosol concentrations in the western and eastern United States and further examine their implications for the national ambient air quality standard of fine aerosol concentrations and for the application of natural visibility condition by the U.S. EPA Regional Haze Rule.

  16. AEROSOL CONCENTRATIONS DURING THE 1999 FRESNO EXPOSURE STUDIES AS FUNCTIONS OF SIZE, SEASON, AND METEOROLOGY

    EPA Science Inventory

    The 1999 Fresno exposure studies took place in February (winter season) and April/May (spring season) for two periods of four weeks. During that time, nearly-continuous measurements of outdoor aerosol concentrations were made with a scanning mobility spectrometer (TSI SNIPS) an...

  17. On-line analysis of urban particulate matter focusing on elevated wintertime aerosol concentrations.

    PubMed

    Tan, Phillip V; Evans, Greg J; Tsai, Julia; Owega, Sandy; Fila, Michael S; Malpica, Oscar; Brook, Jeffrey R

    2002-08-15

    A 10-day winter sampling campaign was conducted in downtown Toronto for particulate matter (PM) air pollution in the fine (<2.5 microm) size range. An aerosol laser ablation mass spectrometer (LAMS), a tapered-element oscillating microbalance (TEOM), and an aerodynamic particle sizer (APS) were operated in parallel to characterize the PM on-line. In this study, the LAMS observed differences in the chemical composition between three separate episodes with higher PM2.5 mass and APS counts. LAMS results showed that in one instance of elevated PM, organic amines were present in the particulates. Temporal analyses of this episode revealed chemical transformations as the amines, characterized by m/z peaks 58(C3HeN)+, 86(C5H2N)+, and nitrates, increased in number concentration while Ca and hydrocarbon particle classes concurrently decreased. On another day, sulfates were found to have increased significantly. The third event was only 4 h in duration and exhibited an increase in the number of submicron-sized K/hydrocarbons and sulfate-containing particles. In this last event, the hydrocarbons and a K to Fe ratio enrichment indicated there was likely a contribution from a combustion source. This work offers some of the first insights into single particle size and chemistry in a cold winter climate.

  18. Simulation of Long-term Changes in the Surface Ozone and Aerosol Concentrations Based on the Solar Activity Data

    NASA Astrophysics Data System (ADS)

    Belan, Boris; Antokhin, Pavel; Arshinov, Mikhail; Belan, Sergey; Slyadneva, Tatyana; Tolmachev, Gennadii

    2010-05-01

    Based on the long-term data obtained during previous studies we have found an interrelationship the surface ozone and aerosol content with solar activity. Variation of the concentration of both these atmospheric components have a period close to 11 years that has a 2(3)-year phase lag with respect to solar activity. Analyzing possible causes of such behaviour we discarded hypotheses of the anthropogenic origin of the trend and post-volcanic influence of El Chichon and Penatubo eruptions. It turned out, that variation of aerosol number concentration correlates with atmospheric circulation forms (W, E, and C), which are governed by solar activity. Then we analysed sequentially an ozone mechanism and variations of incoming ultraviolet radiation to determine possible causes of this phenomenon. As a result we found an intermediate process, which consists in the influence of increasing UV radiation on plants. At the beginning of UV radiation increase it is observed suppression of the vegetation. After 1- or 2-year adaptation period its productivity becomes stronger that leads to the emission of additional amount of ozone and aerosol precursors. This hypothesis has been verified using Normalized Difference Vegetation Index (NDVI) and gave good results. Prediction of the long-term changes in the surface ozone and aerosol concentrations has been done based on this hypothesis. This work was funded by Presidium of RAS (Program No. 16), Brunch of Geology, Geophysics and Mining Sciences of RAS (Program No 5), Russian Foundation for Basic Research (grant No 08-05-92499), and Federal Agency for Science and Innovation (State Contract № 02.518.11.7153).

  19. The Role of Atmospheric Aerosol Concentration on Deep Convective Precipitation: Cloud-Resolving Model Simulations

    NASA Technical Reports Server (NTRS)

    Tao, Wei-Kuo; Li, Xiaowen; Khain, Alexander; Matsui, Toshihisa; Lang, Stephen; Simpson, Joanne

    2010-01-01

    Aerosols and especially their effect on clouds are one of the key components of the climate system and the hydrological cycle [Ramanathan et al., 2001]. Yet, the aerosol effect on clouds remains largely unknown and the processes involved not well understood. A recent report published by the National Academy of Science states "The greatest uncertainty about the aerosol climate forcing - indeed, the largest of all the uncertainties about global climate forcing - is probably the indirect effect of aerosols on clouds NRC [2001]." The aerosol effect on Clouds is often categorized into the traditional "first indirect (i.e., Twomey)" effect on the cloud droplet sizes for a constant liquid water path and the "semi-direct" effect on cloud coverage. The aerosol effect on precipitation processes, also known as the second type of aerosol indirect effect, is even more complex, especially for mixed-phase convective clouds. In this paper, a cloud-resolving model (CRM) with detailed spectral-bin microphysics was used to examine the effect of aerosols on three different deep convective cloud systems that developed in different geographic locations: South Florida, Oklahoma and the Central Pacific, In all three cases, rain reaches the ground earlier for the low CCN (clean) case. Rain suppression is also evident in all three cases with high CCN (dirty) case. However, this suppression only occurs during the first hour of the simulations. During the mature stages of the simulations, the effects of increasing aerosol concentration range from rain suppression in the Oklahoma case, to almost no effect in the Florida case, to rain enhancement in the Pacific case. These results show the complexity of aerosol interactions with convection. The model results suggest that evaporative cooling is a key process in determining whether high CCN reduces or enhances precipitation. Stronger evaporative cooling can produce a stronger cold pool and thus stronger low-level convergence through interactions

  20. Characterization of ultrafine particle number concentration and new particle formation in urban environment of Taipei, Taiwan

    NASA Astrophysics Data System (ADS)

    Cheung, H. C.; Chou, C. C.-K.; Huang, W.-R.; Tsai, C.-Y.

    2013-04-01

    An intensive aerosol characterization experiment was performed at the Taipei Aerosol and Radiation Observatory (TARO, 25.02° N, 121.53° E) in the urban area of Taipei, Taiwan during July 2012. Number concentration and size distribution of aerosol particles were measured continuously, which were accompanied by concurrent measurements of mass concentration of submicron particles, PM (d ≤ 1 μm), and photolysis rate of ozone, J(O1D). The averaged number concentrations of total (Ntotal), accumulation mode (Nacu), Aitken mode (Ntotal), and nucleation mode (Nnuc) particles were 7.6 × 103 cm-3, 1.2 × 103 cm-3, 4.4 × 103 cm-3, and 1.9 × 103 cm-3, respectively. Accordingly, the ultrafine particles (UFPs, d ≤ 100 nm) accounted for 83% of the total number concentration of particles measured in this study (10 ≤ d ≤ 429 nm), indicating the importance of UFPs to the air quality and radiation budget in Taipei and its surrounding areas. An averaged Nnuc/NOx ratio of ~60 cm-3 ppbv-1 was derived from nighttime measurements, which was suggested to be the characteristic of vehicle emissions that contributed to the "urban background" of nucleation mode particles throughout a day. On the contrary, it was found that the number concentration of nucleation mode particles was independent of NOx and could be elevated up to 10 times the "urban background" levels during daytime, suggesting a substantial amount of nucleation mode particles produced from photochemical processes. Consistency in the time series of the nucleation mode particle concentration and the proxy of H2SO4 production, UVB·SO2, for new particle formation (NPF) events showed that photo-oxidation of SO2 was responsible for the formation of new particles in our study area. Moreover, analysis upon the diameter growth rate, GR, and formation rate of nucleation mode particles, J10-25, found that the values of GR (8.5 ± 6.8 nm h-1) in Taipei were comparable to other urban areas, whereas the values of J10-25 (2.2 ± 1

  1. Effects of climate change on aerosol concentrations in Europe

    NASA Astrophysics Data System (ADS)

    Megaritis, Athanasios G.; Fountoukis, Christos; Pandis, Spyros N.

    2013-04-01

    High concentrations of particulate matter less than 2.5 μm in size (PM2.5), ozone and other major constituents of air pollution, have adverse effects on human health, visibility and ecosystems (Seinfeld and Pandis, 2006), and are strongly influenced by meteorology. Emissions control policy is currently made assuming that climate will remain constant in the future. However, climate change over the next decades is expected to be significant (IPCC, 2007) and may impact local and regional air quality. Determining the sensitivity of the concentrations of air pollutants to climate change is an important step toward estimating future air quality. In this study we applied PMCAMx (Fountoukis et al., 2011), a three dimensional chemical transport model, over Europe, in order to quantify the individual effects of various meteorological parameters on fine particulate matter (PM2.5) concentrations. A suite of perturbations in various meteorological factors, such as temperature, wind speed, absolute humidity and precipitation were imposed separately on base case conditions to determine the sensitivities of PM2.5 concentrations and composition to these parameters. Different simulation periods (summer, autumn 2008 and winter 2009) are used to examine also the seasonal dependence of the air quality - climate interactions. The results of these sensitivity simulations suggest that there is an important link between changes in meteorology and PM2.5 levels. We quantify through separate sensitivity simulations the processes which are mainly responsible for the final predicted changes in PM2.5 concentration and composition. The predicted PM2.5 response to those meteorology perturbations was found to be quite variable in space and time. These results suggest that, the changes in concentrations caused by changes in climate should be taken into account in long-term air quality planning. References Fountoukis C., Racherla P. N., Denier van der Gon H. A. C., Polymeneas P., Charalampidis P. E

  2. Aircraft observations of aerosol and trace gas concentrations in the tropical troposphere up to 12 km during the INCA campaign

    NASA Astrophysics Data System (ADS)

    Minikin, A.; Baehr, J.; Krejci, R.; Schlager, H.; van Velthoven, P.; Seifert, M.; Ström, J.; Petzold, A.; Schumann, U.

    2003-04-01

    During the EU funded project INCA (Interhemispheric differences in cirrus properties from anthropogenic emissions) the DLR Falcon 20, a German research aircraft with a maximum ceiling of 13~km, carried out measurements of aerosol and trace gas concentrations during transfer from Europe to South America and back in order to obtain meridional cross sections between 50^o~N and 50^o~S. At tropical latitudes the southbound transfer flights were directed along the west coast of South America, whereas the northbound transfer flights passed over Brazil and the central Atlantic Ocean. We report on observational data of number concentrations of Aitken and accumulation mode particles, the fractionation between volatile and non-volatile particles, as well as mixing ratios of carbon monoxide, reactive nitrogen species and ozone. In the tropics aerosol number concentrations above 9~km altitude increase by one order of magnitude, if compared to the sub-tropics and mid-latitudes, most pronounced for refractory particles. These elevated aerosol concentrations occur where 3-dimensional back trajectories originate from the central South American continent (Amazon basin) and have undergone systematic uplifting. The very high fraction of refractory particles, up to 50--60~% of total condensation nuclei, may indicate a strong contribution of continental ground sources. The INCA measurements confirm earlier TROPOZ II observations of an extended upper tropospheric layer of enhanced CO and NO over tropical South America during the wet season. Vertical distributions show a striking increase of CO mixing ratios above 6~km. Corresponding increases of NO and NOy and decreases of ozone were also found. During INCA an anticyclonic flow over tropical South America was persistent in the upper troposphere. This upper-level anticyclone is associated with intense convective activity over the Amazon basin and redistributes the convectively lifted air masses over a large area in the tropical middle

  3. Concentration characteristics of bromine and iodine in aerosols in Shanghai, China

    NASA Astrophysics Data System (ADS)

    Gao, Yunchuan; Sun, Mingxing; Wu, Xiaowei; Liu, Yongdi; Guo, Yaqi; Wu, Ji

    2010-11-01

    Aerosol samples (TSP and PM 10) during each season were collected at a national monitoring point in Shanghai in 2008. Halogens (Br, I) were determined in samples along with sodium (Na) by ICP-MS and ICP-OES after microwave digestion. In this report we focused on the concentration characteristics of halogen elements Br and I and their seasonal distributions. The mean annual concentrations of total Br and I were 24 ng m -3 and 12 ng m -3 for TSP, 21 ng m -3 and 9 ng m -3 for PM 10, respectively. Concentrations of Br and I in TSP and PM 10 were lowest in summer but an increase occurred in autumn and winter. Water-soluble Br and I accounted for about 32% of the total Br and I in aerosols, and about 68% of Br and I was non soluble which may be non-soluble organic species. These non-soluble organic species are present in aerosols in the possible binding forms as mineral dust, natural organic matter, and adsorption to black carbon or mineral material such as iron oxides. Soluble Br and I in PM 10 extracted by a dilute acid solution (HNO 3 + H 2SO 4) increased by 22% and 18%, respectively, compared with water-soluble Br and I. A positive correlation with Na and sea water enrichment factors for Br and I indicated that bromine and iodine in aerosols originated mostly from marine sources in Shanghai.

  4. Thyroid CT number and its relationship to iodine concentration

    SciTech Connect

    Iida, Y.; Konishi, J.; Harioka, T.; Misaki, T.; Endo, K.; Torizuka, K.

    1983-06-01

    Sixty-seven patients with thyroid disease and 24 normal controls were examined with computed tomography (CT). The mean CT number (Hounsfield units +/- SD) in the normal controls (118.1 +/- 12.2) was significantly higher (p < 0.001) than the mean CT number in patients with diseased thyroids, except for 2 cases of simple goiter (CT numbers 113, 132). The Graves disease (69.5 +/- 17.6) amd Hishimoto thyroiditis (61.4 +/- 9.1) were significaantly higher than those in patients with adenoma (41.7 +/- 10.6, p < 0.001), cyst (33.1 +/- 14.8, p < 0.001), or cancer (48.7 +/- 13, p < 0.01). In 14 patients studied, a significant correlation was observed between thyroid CT numbers and the iodine concentration of the tissue (r = 0.889; p < 0.001).

  5. Modeling source contributions to submicron particle number concentrations measured in Rochester, New York

    SciTech Connect

    Ogulei, D.; Hopke, P.K.; Chalupa, D.C.; Utell, M.J.

    2007-02-15

    An advanced receptor model was used to elicit source information based on ambient submicron (0.01-0.47 {mu}m) particle number concentrations, gaseous species, and meteorological variables measured at the New York State Department of Environmental Conservation central monitoring site in Rochester, NY. Four seasonal data sets (winter, spring, summer, and fall) were independently investigated. A total of ten different sources were identified, including two traffic factors, two nucleation factors, industrial emissions, residential/commercial heating, secondary nitrate, secondary sulfate, ozone-rich secondary aerosol, and regionally transported aerosol. The resolved sources were generally characterized by similar number modes for either winter, spring, summer or fall. The size distributions for nucleation were dominated by the smallest particles ({lt}10-30 nm) that gradually grew to larger sizes as could be seen by observing the volume profiles. In addition, the nucleation factors were closely linked to traffic rush hours suggesting that cooling of tail-pipe emissions may have induced nucleation activity in the vicinity of the highways. Industrial emissions were dominated by emissions from coal-fired power plants that were located to the northwest of the sampling site. These facilities represent the largest point emission sources of SO{sub 2}, and probably ultrafine ({lt}0.1 {mu}m) or submicron particles, in Rochester. Regionally transported material was characterized by accumulation mode particles. Air parcel back-trajectories showed transport of air masses from the industrial midwest.

  6. Black Carbon Concentration from Worldwide Aerosol Robotic Network (AERONET) Measurements

    NASA Technical Reports Server (NTRS)

    Schuster, Gregory L.; Dubovik, Oleg; Holben, Brent N.; Clothiaux, Eugene E.

    2006-01-01

    The carbon emissions inventories used to initialize transport models and general circulation models are highly parameterized, and created on the basis of multiple sparse datasets (such as fuel use inventories and emission factors). The resulting inventories are uncertain by at least a factor of 2, and this uncertainty is carried forward to the model output. [Bond et al., 1998, Bond et al., 2004, Cooke et al., 1999, Streets et al., 2001] Worldwide black carbon concentration measurements are needed to assess the efficacy of the carbon emissions inventory and transport model output on a continuous basis.

  7. Simulations of organic aerosol concentrations during springtime in the Guanzhong Basin, China

    NASA Astrophysics Data System (ADS)

    Feng, Tian; Li, Guohui; Cao, Junji; Bei, Naifang; Shen, Zhenxing; Zhou, Weijian; Liu, Suixin; Zhang, Ting; Wang, Yichen; Huang, Ru-jin; Tie, Xuexi; Molina, Luisa T.

    2016-08-01

    The organic aerosol (OA) concentration is simulated in the Guanzhong Basin, China from 23 to 25 April 2013 utilizing the WRF-CHEM model. Two approaches are used to predict OA concentrations: (1) a traditional secondary organic aerosol (SOA) module; (2) a non-traditional SOA module including the volatility basis-set modeling method in which primary organic aerosol (POA) is assumed to be semivolatile and photochemically reactive. Generally, the spatial patterns and temporal variations of the calculated hourly near-surface ozone and fine particle matters agree well with the observations in Xi'an and surrounding areas. The model also yields reasonable distributions of daily PM2.5 and elemental carbon (EC) compared to the filter measurements at 29 sites in the basin. Filter-measured organic carbon (OC) and EC are used to evaluate OA, POA, and SOA using the OC / EC ratio approach. Compared with the traditional SOA module, the non-traditional module significantly improves SOA simulations and explains about 88 % of the observed SOA concentration. Oxidation and partitioning of POA treated as semivolatile constitute the most important pathway for the SOA formation, contributing more than 75 % of the SOA concentrations in the basin. Residential emissions are the dominant anthropogenic OA source, constituting about 50 % of OA concentrations in urban and rural areas and 30 % in the background area. The OA contribution from transportation emissions decreases from 25 % in urban areas to 20 % in the background area, and the industry emission OA contribution is less than 6 %.

  8. Trace metal concentration in Trade Wind aerosols collected over Barbados and Miami.

    NASA Astrophysics Data System (ADS)

    Trapp, J. M.; Millero, F. J.; Prospero, J. M.

    2007-12-01

    African mineral dust aerosols are transported by trade winds to Barbados and often reach Miami. The trace metals contained in these aerosols play an important role in biogeochemical processes and thus the global carbon cycle. High-volume bulk aerosols were collected in the summer dust season (June-September) of 2003 and 2004 in Miami and Barbados on Whatman-41 filters and microwave digested using a modified version of EPA method 3051. Aliquots of digested samples were tested for trace metal concentrations by ICP-MS. Excellent agreement with gravimetrically determined ashed weights was observed with dust concentrations calculated based on Al crustal abundance. As a major component, aluminum averaged 8.7% content in agreement to 8.1% crustal abundance, and was used to examine other trace metals. Al, Fe, V, Cr, Mn, Cu, Co, Ni, Zn, As, Tl, Ba, Cd, Pb and REE's were examined and deviations from average crustal abundance are discussed in relationship to temporal variation and meteorological conditions. In addition, trace metal pollutants in Miami aerosols were examined relative to the relatively clean samples offered by Barbados.

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

    NASA Astrophysics Data System (ADS)

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

    2017-02-01

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

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

    NASA Astrophysics Data System (ADS)

    Yttri, K. E.; Dye, C.; Kiss, G.

    2007-08-01

    Sugars and sugar-alcohols are demonstrated to be important constituents of the ambient aerosol water-soluble organic carbon fraction, and to be tracers for primary biological aerosol particles (PBAP). In the present study, levels of four sugars (fructose, glucose, sucrose, trehalose) and three sugar-alcohols (arabitol, inositol, mannitol) in ambient aerosols have been quantified using a novel HPLC/HRMS-TOF (High Performance Liquid Chromatography in combination with High Resolution Mass Spectrometry - Time of Flight) method to assess the contribution of PBAP to PM>sub>10 and PM2.5. Samples were collected at four sites in Norway at different times of the year in order to reflect the various contributing sources and the spatial and seasonal variation of the selected compounds. Sugars and sugar-alcohols were present at all sites investigated, underlining the ubiquity of these highly polar organic compounds. The highest concentrations were reported for sucrose, reaching a maximum concentration of 320 ng m-3 in PM10 and 55 ng m-3 in PM2.5. The mean concentration of sucrose was up to 10 times higher than fructose, glucose and the dimeric sugar trehalose. The mean concentrations of the sugar-alcohols were typically lower, or equal, to that of the monomeric sugars and trehalose. Peak concentrations of arabitol and mannitol did not exceed 30 ng m-3 in PM10, and for PM2.5 all concentrations were below 6 ng m-3. Sugars and sugar-alcohols were associated primarily with coarse aerosols except during wintertime at the suburban site in Elverum, where a shift towards sub micron aerosols was observed. It is proposed that this shift was due to the intensive use of wood burning for residential heating at this site during winter, confirmed by high concurrent concentrations of levoglucosan. Elevated concentrations of sugars in PM2.5 were observed during spring and early summer at the rural background site Birkenes. It is hypothesized that this was due to ruptured pollen.

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

    PubMed

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

    2012-03-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2017-03-01

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

  13. The Influence of High Aerosol Concentration on Atmospheric Boundary Layer Temperature Stratification

    SciTech Connect

    Khaykin, M.N.; Kadygrove, E.N.; Golitsyn, G.S.

    2005-03-18

    Investigations of the changing in the atmospheric boundary layer (ABL) radiation balance as cased by natural and anthropogenic reasons is an important topic of the U.S. Department of Energy's Atmospheric Radiation Measurement (ARM) program. The influence of aerosol on temperature stratification of ABL while its concentration was extremely high within a long period of time was studied experimentally. The case was observed in Moscow region (Russia) with the transport of combustion products from peat-bog and forest fires in July-September, 2002. At this time the visibility was some times at about 100-300 m. Aerosol concentration measured by Moscow University Observatory and A.M. Obukhov Institute of Atmospheric Physics field station in Zvenigorod (55.7 N; 36.6 E) for several days was in 50-100 times more than background one (Gorchakov at al 2003). The high aerosol concentration can change the radiation balance at ABL, and so to change thermal stratification in ABL above the mega lopolis. For the analysis the data were used of synchronous measurements by MTP-5 (Microwave Temperature Profiler operating at wavelength 5 mm) in two locations, namely: downtown Moscow and country-side which is 50 km apart to the West (Zvenigorod station). (Kadygrov and Pick 1998; Westwater at al 1999; Kadygrov at al 2002). Zvenigorod station is located in strongly continental climate zone which is in between of the climates of ARM sites (NSANorth Slope of Alaska and SGP-Southern Great Plains). The town of Zvenigorod has little industry, small traffic volume and topography conductive to a good air ventilation of the town. For these reasons Zvenigorod can be considered as an undisturbed rural site. For the analysis some days were chosen with close meteorological parameters (average temperature, humidity, wind, pressure and cloud form) but strongly differing in aerosol concentration level.

  14. Influence of a high aerosol concentration on the thermal structure of the atmospheric boundary layer

    NASA Astrophysics Data System (ADS)

    Khaikin, M. N.; Kuznetsova, I. N.; Kadygrov, E. N.

    2006-12-01

    The influence of increased concentrations of submicron aerosol produced by forest fires on thermal characteristics of the atmospheric boundary layer (ABL) in Moscow and its remote vicinity (the town of Zvenigorod) are analyzed on the basis of regular remote measurements of the ABL temperature profile with the use of MTP-5 profilers. In the air basin of a large city, additional aerosol and accompanying pollutants in early morning hours (at small heights of the Sun) most frequently did not cause substantial changes in the ABL thermal structure. In the locality remote from the megalopolis (Zvenigorod), the atmospheric pollution by aerosol led to noticeable changes in the ABL thermal characteristics. Especially strong changes were observed in the daytime, during the maximum supply of solar radiation. In morning hours, the heating rate of the lower 100-m layer of the polluted air exceeded the heating rate of a relatively pure air by more than one degree. In higher layers, the differences between the rates of temperature changes in a relatively clean atmosphere and in an atmosphere polluted by aerosol (in the suburb) were insignificant.

  15. Effect of high concentrations of inorganic seed aerosols on secondary organic aerosol formation in the m-xylene/NO x photooxidation system

    NASA Astrophysics Data System (ADS)

    Lu, Zifeng; Hao, Jiming; Takekawa, Hideto; Hu, Lanhua; Li, Junhua

    High concentrations (>15 μm 3 cm -3) of CaSO 4, Ca(NO 3) 2 and (NH 4) 2SO 4 were selected as surrogates of dry neutral, aqueous neutral and dry acidic inorganic seed aerosols, respectively, to study the effects of inorganic seeds on secondary organic aerosol (SOA) formation in irradiated m-xylene/NO x photooxidation systems. The results indicate that neither ozone formation nor SOA formation is significantly affected by the presence of neutral aerosols (both dry CaSO 4 and aqueous Ca(NO 3) 2), even at elevated concentrations. The presence of high concentrations of (NH 4) 2SO 4 aerosols (dry acidic) has no obvious effect on ozone formation, but it does enhance SOA generation and increase SOA yields. In addition, the effect of dry (NH 4) 2SO 4 on SOA yield is found to be positively correlated with the (NH 4) 2SO 4 surface concentration, and the effect is pronounced only when the surface concentration reaches a threshold value. Further, it is proposed that the SOA generation enhancement is achieved by particle-phase heterogeneous reactions induced and catalyzed by the acidity of dry (NH 4) 2SO 4 seed aerosols.

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

    NASA Astrophysics Data System (ADS)

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

    2016-07-01

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

  17. Final Report, The Influence of Organic-Aerosol Emissions and Aging on Regional and Global Aerosol Size Distributions and the CCN Number Budget

    SciTech Connect

    Donahue, Neil M.

    2015-12-23

    We conducted laboratory experiments and analyzed data on aging of organic aerosol and analysis of field data on volatility and CCN activity. With supplemental ASR funding we participated in the FLAME-IV campaign in Missoula MT in the Fall of 2012, deploying a two-chamber photochemical aging system to enable experimental exploration of photochemical aging of biomass burning emissions. Results from that campaign will lead to numerous publications, including demonstration of photochemical production of Brown Carbon (BrC) from secondary organic aerosol associated with biomass burning emissions as well as extensive characterization of the effect of photochemical aging on the overall concentrations of biomass burning organic aerosol. Excluding publications arising from the FLAME-IV campaign, project research resulted in 8 papers: [11, 5, 3, 10, 12, 4, 8, 7], including on in Nature Geoscience addressing the role of organic compounds in nanoparticle growth [11

  18. Fungal Spore Concentrations and Ergosterol Content in Aerosol Samples in the Caribbean During African Dust Events

    NASA Astrophysics Data System (ADS)

    Santos-Figueroa, G.; Bolaños-Rosero, B.; Mayol-Bracero, O. L.

    2015-12-01

    Fungal spores are a major component of primary biogenic aerosol particles that are emitted to the atmosphere, are ubiquitous, and play an important role in the chemistry and physics of the atmosphere, climate, and public health. Every year, during summer months, African dust (AD) particles are transported to the Caribbean region causing an increase in the concentrations of particulate matter in the atmosphere. AD is one of the most important natural sources of mineral particulate matter at the global scale, and many investigations suggest that it has the ability to transport dust-associated biological particles through long distances. The relationship between AD incursions and the concentration of fungal spores in the Caribbean region is poorly understood. In order to investigate the effects of AD incursions on fungal spore's emissions, fungal spore concentrations were monitored using a Burkard spore trap at the tropical montane cloud forest of Pico del Este at El Yunque National Forest, Puerto Rico. The presence of AD was supported with satellite images of aerosol optical thickness, and with the results from the air masses backward trajectories calculated with the NOAA HYSPLIT model. Basidiospores and Ascospores comprised the major components of the total spore's concentrations, up to a maximum of 98%, during both AD incursions and background days. A considerably decrease in the concentration of fungal spores during AD events was observed. Ergosterol, biomarker for measuring fungal biomass, concentrations were determined in aerosols that were sampled at a marine site, Cabezas de San Juan Nature Reserve, in Fajardo Puerto Rico, and at an urban site, Facundo Bueso building at the University of Puerto Rico. Additional efforts to understand the relationship between the arrival of AD to the Caribbean and a decrease in spore's concentrations are needed in order to investigate changes in local spore's vs the contribution of long-range spores transported within the AD.

  19. Estimation of surface area concentration of workplace incidental nanoparticles based on number and mass concentrations

    NASA Astrophysics Data System (ADS)

    Park, J. Y.; Ramachandran, G.; Raynor, P. C.; Kim, S. W.

    2011-10-01

    Surface area was estimated by three different methods using number and/or mass concentrations obtained from either two or three instruments that are commonly used in the field. The estimated surface area concentrations were compared with reference surface area concentrations (SAREF) calculated from the particle size distributions obtained from a scanning mobility particle sizer and an optical particle counter (OPC). The first estimation method (SAPSD) used particle size distribution measured by a condensation particle counter (CPC) and an OPC. The second method (SAINV1) used an inversion routine based on PM1.0, PM2.5, and number concentrations to reconstruct assumed lognormal size distributions by minimizing the difference between measurements and calculated values. The third method (SAINV2) utilized a simpler inversion method that used PM1.0 and number concentrations to construct a lognormal size distribution with an assumed value of geometric standard deviation. All estimated surface area concentrations were calculated from the reconstructed size distributions. These methods were evaluated using particle measurements obtained in a restaurant, an aluminum die-casting factory, and a diesel engine laboratory. SAPSD was 0.7-1.8 times higher and SAINV1 and SAINV2 were 2.2-8 times higher than SAREF in the restaurant and diesel engine laboratory. In the die casting facility, all estimated surface area concentrations were lower than SAREF. However, the estimated surface area concentration using all three methods had qualitatively similar exposure trends and rankings to those using SAREF within a workplace. This study suggests that surface area concentration estimation based on particle size distribution (SAPSD) is a more accurate and convenient method to estimate surface area concentrations than estimation methods using inversion routines and may be feasible to use for classifying exposure groups and identifying exposure trends.

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

    NASA Astrophysics Data System (ADS)

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

    2016-12-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2014-12-01

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

  2. Non-spherical aerosol transport under oscillatory shear flows at low-Reynolds numbers

    NASA Astrophysics Data System (ADS)

    Shachar Berman, Lihi; Delorme, Yann; Hofemeier, Philipp; Frankel, Steven; Sznitman, Josue

    2014-11-01

    Most airborne particles are intrinsically non-spherical. In particular, non-spherical particles with high aspect ratios, such as fibers, are acknowledged to be more hazardous than their spherical counterparts due to their ability to penetrate into deeper lung regions, causing serious pulmonary diseases. Not only do particle properties such as size, shape, and density have a major impact on particle transport, for non-spherical aerosols, their orientations also greatly influence particle trajectories due to modified lift and drag characteristics. Until present, however, most of our understanding of the dynamics of inhaled particles in the deep airways of the lungs has been limited to spherical particles only. In the present work, we seek to quantify through numerical simulations the transport of non-spherical airborne particles and their deposition under oscillatory shear flows at low Reynolds numbers, characteristic of acinar airways. Here, the Euler-Lagrangian model is used to solve the translational movement of a fiber, whereas the Eulerian rotational equations are introduced and solved to predict detailed unsteady fiber orientations. Overall, our efforts provide new insight into realistic dynamics of inhaled non-spherical aerosols under characteristic breathing motions.

  3. MODELING THE EFFECT OF CHLORINE EMISSIONS ON ATMOSPHERIC OZONE AND SECONDARY ORGANIC AEROSOL CONCENTRATIONS ACROSS THE UNITED STATES

    EPA Science Inventory

    This paper presents the modeled effects of natural and anthropogenic chlorine emissions on the atmospheric concentrations of ozone and secondary organic aerosol across the United States. The model calculations include anthropogenic molecular chlorine emissions, anthropogenic hypo...

  4. Local aerosol concentrations and optical characteristics influenced by the Indonesian forest fire

    NASA Astrophysics Data System (ADS)

    Ru, Jianfei; Minomura, Mitsuo; Kuze, Hiroaki; Takeuchi, Nobuo

    1998-08-01

    Indonesian forest fire took place on Kalimantan and Sumatera islands in 1997 and continuously influenced the atmospheric conditions of South-East Asia nearly throughout the last half of that year. The color composed images of visible, near IR and IR channels from NOAA AVHRR daily data, arbitrarily assigned to red, green and blue respectively, were synthesized for distinguishing the smoke area. The data of three periods, the beginning, mid, and ending parts of the fire, were collected and analyzed in order to show the variation of atmosphere with the development of fire. A retrieval algorithm was established by use of Mie theory calculation and the radiative transfer codes. Local aerosol concentrations and properties over ocean parts between the two islands were derived. It is found that the aerosol optical thickness increased in accordance with the exacerbation of the fires. The changes of angstrom exponents show that smaller particle amounts were raised by the effects of burning.

  5. Is It Possible to Distinguish Between Dust and Salt Aerosol Over Waters with Unknown Chlorophyll Concentrations Using Spectral Remote Sensing?

    NASA Technical Reports Server (NTRS)

    Levy, R. C.; Kaufman, Y. J.

    1999-01-01

    Atmospheric aerosol has uncertain impacts on the global climate system, as well as on atmospheric and bio-geo-chemical processes of regional and local scales. EOS-MODIS is one example of a satellite sensor designed to improve understanding of the aerosols' type, size and distribution at all temporal and spatial scales. Ocean scientists also plan to use data from EOS-MODIS to assess the temporal and spatial coverage of in-water chlorophyll. MODIS is the first sensor planned to observe the combined ocean-atmosphere system with a wide spectral range (from 410 to 2200 nm). Dust aerosol and salt aerosol have similar spectral signals for wavelengths longer than 550 nm, but because dust selectively absorbs blue light, they have divergent signals in the blue wavelength regions (412 to 490 nm). Chlorophyll also selectively absorbs blue radiation, so that varying chlorophyll concentrations produces a highly varying signal in the blue regions, but less variability in the green, and almost no signal in the red to mid-infrared regions. Thus, theoretically, it may be difficult to differentiate dust and salt in the presence of unknown chlorophyll in the ocean. This study attempts to address the cases in which aerosol and chlorophyll signals can and cannot be separated. For the aerosol spectra, we use the aerosol lookup table from the operational MODIS aerosol-over-ocean algorithm, and for chlorophyll spectra, we use the SeaBAM data set (created for SeaWiFS). We compare the signals using Principal Component Analysis and attempt to retrieve both chlorophyll and aerosol properties using a variant of the operational MODIS aerosol-over-ocean algorithm. Results show that for small optical depths, less than 0.5, it is not possible to differentiate between dust and salt and to determine the chlorophyll concentration at the same time. For larger aerosol optical depths, the chlorophyll signals are comparatively insignificant, and we can hope to distinguish between dust and salt.

  6. Relating Aerosol Profile and Column Measurements to Surface Concentrations: What Have We Learned from Discover-AQ?

    NASA Astrophysics Data System (ADS)

    Hoff, R. M.

    2014-12-01

    One research goal of the Deriving Information on Surface Conditions from COlumn and VERtically Resolved Observations Relevant to Air Quality (DISCOVER-AQ) mission was to determine sufficient column profile measurements to relate column integrated quantities such as Aerosol Optical Depth to surface concentrations. I will review the relationship between AOD and PM2.5 at the surface. DISCOVER-AQ in Baltimore, the San Joaquin Valley, Houston and Denver revealed quite different conditions for determining this relationship. In each case, the surface reflectivity made determination of aerosol optical depth challenging, but upward looking columns of aerosol optical depth from sunphotometers provided confirmation of the AOD results from space. In Baltimore, AOD fields reflected PM2.5 concentrations well. In California, however, the low boundary layer heights and dominance of nitrate and organic aerosols made the AOD fields less predictive of PM2.5. In California and Colorado, hydration of the aerosol varied dramatically with aerosol type (especially smoke and dust) and revealed that without an understanding of the degree of aerosol hydration with aerosol composition, the relationship between AOD and PM2.5 will continue to be a challenge. Model predictions in the Baltimore-Washington study are relatively disappointing in helping define the needed physics between the optical and microphysical properties. An overview of the measurements from DISCOVER-AQ which will help define the needed information in a more general case in the future will be given.

  7. Aerosols and gases concentrations observed at Stelvio National Park (Italian Alps) during summer conditions

    NASA Astrophysics Data System (ADS)

    Landi, T. C.; Marinoni, A.; Cristofanelli, P.; Bonafè, U.; Calzolari, F.; Duchi, R.; Laj, P.; Villani, P.; Bonasoni, P.

    2012-04-01

    Three summer fields campaigns were carried out during 2009, 2010 and 2011 in two sites in the area of Stelvio National Park (SNP), Central Italian Alps. Those activities were performed in the frame of the SHARE - Stelvio project (Station at High Altitude for Research on the Environment). SNP includes an extensive impervious territory of valleys and high mountains, up to 3900 m asl. Two high altitude sampling sites, Rifugio Guasti (3285 m asl) and Forni glacier ( 2700 m asl), have been picked out for collecting the main atmospheric parameters: the first site hosted the field campaign in 2009 and 2010 and was located at Cevedale pass, at the border between Lombardia and Trentino-Alto Adige regions, while in 2011 the measurements were carried out on Forni glacier surface, in a N-S oriented valley, through SHARE-box, a portable and autonomous unit for atmospheric measurements developed in the framework of SHARE project. Because of different location Rifugio Guasti is an ideal site to monitor long range transport on Southern slope of Alpine range, while Forni glacier is more affected by local influence of valley and glacier breezes. Monitored parameters concerned (i) meteorology, such as air temperature, relative humidity, wind speed and direction, air pressure, (ii) chemical and physical properties of the aerosols (number concentrations, size distribution and chemical composition) and (iii) , gases concentration (CO2, O3). This work is aimed at describing the behaviour of these compounds, in terms of concentration observed over different time scales, such hourly and daily, in order to investigate the impact of transport processes (i.e. air masses transports arisen from both "thermal" breezes or synoptic circulation) on aerosols and gases variability at SNP. The Alps face the Po Valley, one of the more populated and industrialized region in Europe. This is one of the most probable source of polluted air masses which spread towards high altitude sites, such as Alps and

  8. Susceptibility of Tribolium confusum (Coleoptera: Tenebrionidae) to pyrethrin aerosol: effects of aerosol particle size, concentration, and exposure conditions

    Technology Transfer Automated Retrieval System (TEKTRAN)

    A series of laboratory studies were conducted to assess effect of droplet size on efficacy of pyrethrin aerosol against adults of Tribolium confusum Jacqueline DuVal, the confused flour beetle. A vertical flow aerosol exposure chamber that generated a standardized particle size diameter was used for...

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

    NASA Astrophysics Data System (ADS)

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

    2016-11-01

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

  10. Temporal variations in sources and concentrations of black and organic carbon aerosols in the LA Basin

    NASA Astrophysics Data System (ADS)

    Mouteva, G.; Kearney, J.; Fahrni, S.; Santos, G. M.; Czimczik, C. I.

    2012-12-01

    Temporal variations in sources and concentrations of black and organic carbon aerosols in the LA Basin Black carbon (BC), derived from incomplete combustion of fossil and biogenic fuels and vegetation fires, is a crucial component of the aerosol pool, but sources as well as atmospheric transport and lifetime remain poorly constrained by measurements. We characterized the composition of carbonaceous aerosols emitted from urban areas by quantifying the temporal variations in the concentrations and sources of BC and organic carbon (OC) in PM-10 and PM-2.5 from two locations in the Los Angeles basin. Using the radiocarbon signatures in BC and OC allowed us to apportion emissions into fossil and modern contributions. We separated and quantified BC and OC using a modified Sunset OC-EC analyzer coupled to a vacuum line and cryogenically trapped the evolving CO2 (Zhang et al. In Prep.). The instrument and method were tested with well-defined radiocarbon standards to determine background, accuracy and precision. The purified CO2 was converted to graphite and measured at the Keck-AMS facility on unknown samples as small as ≥5 μg C. Preliminary results suggest that radiocarbon content can be used to apportion BC into fossil and modern sources. BC concentrations are on the order of 6-31% total carbon, with 48 to 96% fossil contribution. In the OC fraction we detected several super-modern samples, suggesting local production of radiocarbon, e.g. from medical waste incinerators. Thus, the radiocarbon-based approach cannot be used to quantify sources of OC and bulk carbonaceous aerosols in urban areas. Our measurements contribute to a comprehensive quantification of temporal and spatial variations in urban BC, a key uncertainty in constraining BC sources and transport in North America. References: Zhang YL, Perron N, Zotter P, Minguillón MC, Wacker L, Prévôt ASH, Baltensperger U, Szidat S. In Prep. On the isolation of OC and EC and the optimal strategy of radiocarbon

  11. Number-size distribution of aerosol particles and new particle formation events in tropical and subtropical Pacific Oceans

    NASA Astrophysics Data System (ADS)

    Ueda, S.; Miura, K.; Kawata, R.; Furutani, H.; Uematsu, M.; Omori, Y.; Tanimoto, H.

    2016-10-01

    Number-size distributions of aerosol particles with diameters of 10-500 nm in the marine boundary layer were observed continually onboard the R/V Hakuho Maru over the equatorial and subtropical North Pacific and South Pacific during December 2011-March 2012. Number-size distributions over each area were parameterized using a sum of up to three lognormal functions. Bi-modal size distributions with peak diameters at 30-80 nm (Aitken mode) and 100-200 nm (accumulation mode) were observed frequently. Larger peak diameters of Aitken and accumulation modes were observed over the eastern equator, where 5-day backward trajectories showed that the air masses had derived from high-chlorophyll oceanic regions without precipitation. Smaller peak diameters and low concentrations were often observed over the North Pacific. The trajectories show that such air mass originated from oceanic regions with less chlorophyll, exhibiting high precipitation frequency. New particle formation (NPF) events have often been observed over the mid-latitude eastern South Pacific with a low condensation sink (CS) and some dimethyl sulfide, although none was observed over the equator, where CS was higher. The lesser CS condition at NPF events was mostly correlated with local precipitation or precipitation along the trajectories within 1 day. These results suggest that differences of the number-size distribution and occasions of NPF events among sea areas most closely accord with precipitation along the trajectories.

  12. A CLOSURE STUDY OF AEROSOL MASS CONCENTRATION MEASUREMENTS: COMPARISON OF VALUES OBTAINED WITH FILTERS AND BY DIRECT MEASUREMENTS OF MASS DISTRIBUTIONS. (R826372)

    EPA Science Inventory

    We compare measurements of aerosol mass concentrations obtained gravimetrically using Teflon coated glass fiber filters and by integrating mass distributions measured with the differential mobility analyzer–aerosol particle mass analyzer (DMA–APM) technique (Aero...

  13. Daily concentration variations of nitrate in the atmospheric aerosols voer Sakai, Japan

    SciTech Connect

    Mizohata, Akira; Ito, Norio

    1996-12-31

    Atmospheric aerosols have been sampled on a quartz fiber filter on a daily basis in Sakai, Japan since 1986. The obtained filter samples were extracted with distilled water, and ionic species concentrations were quantitatively determined by using ion chromatography. In this paper study of the nitrate concentration was described. Analysis showed that the mean concentration for period January 1986 to December 1993 was 2.4 {mu}g/m{sup 3}. Monthly mean was in the range of 0.9 to 3.9 {mu}g/m{sup 3}, and highest in April and lowest in August. Especially the concentrations for period March to June 1991 were remarkably high because of the Kuwait oil well fire due to the Gulf War. Annual mean was increasing over a long period of time. Explaining this trend and the seasonal variations, we considered air mass trajectories.

  14. Estimation of surface-level PM concentration from satellite observation taking into account the aerosol vertical profiles and hygroscopicity.

    PubMed

    Kim, Kwanchul; Lee, Kwon H; Kim, Ji I; Noh, Youngmin; Shin, Dong H; Shin, Sung K; Lee, Dasom; Kim, Jhoon; Kim, Young J; Song, Chul H

    2016-01-01

    Surface-level PM10 distribution was estimated from the satellite aerosol optical depth (AOD) products, taking the account of vertical profiles and hygroscopicity of aerosols over Jeju, Korea during March 2008 and October 2009. In this study, MODIS AOD data from the Terra and Aqua satellites were corrected with aerosol extinction profiles and relative humidity data. PBLH (Planetary Boundary Layer Height) was determined from MPLNET lidar-derived aerosol extinction coefficient profiles. Through statistical analysis, better agreement in correlation (R = 0.82) between the hourly PM10 concentration and hourly average Sunphotometer AOD was the obtained when vertical fraction method (VFM) considering Haze Layer Height (HLH) and hygroscopic growth factor f(RH) was used. The validity of the derived relationship between satellite AOD and surface PM10 concentration clearly demonstrates that satellite AOD data can be utilized for remote sensing of spatial distribution of regional PM10 concentration.

  15. Characterization of ultrafine particle number concentration and new particle formation in an urban environment of Taipei, Taiwan

    NASA Astrophysics Data System (ADS)

    Cheung, H. C.; Chou, C. C.-K.; Huang, W.-R.; Tsai, C.-Y.

    2013-09-01

    An intensive aerosol characterization experiment was performed at the Taipei Aerosol and Radiation Observatory (TARO, 25.02° N, 121.53° E) in the urban area of Taipei, Taiwan, during July 2012. Number concentration and size distribution of aerosol particles were measured continuously, which were accompanied by concurrent measurements of mass concentration of submicron particles, PM1 (d ≤ 1 μm), and photolysis rate of ozone, J(O1D). The averaged number concentrations of total (Ntotal), accumulation mode (Nacu), Aitken mode (NAitken), and nucleation mode (Nnuc) particles were 13.9 × 103 cm-3, 1.2 × 103 cm-3, 6.1 × 103 cm-3, and 6.6 × 103 cm-3, respectively. Accordingly, the ultrafine particles (UFPs, d ≤ 100 nm) accounted for 91% of the total number concentration of particles measured in this study (10 ≤ d ≤ 429 nm), indicating the importance of UFPs to the air quality and radiation budget in Taipei and its surrounding areas. An averaged Nnuc / NOx ratio of 192.4 cm-3 ppbv-1 was derived from nighttime measurements, which was suggested to be the characteristic of vehicle emissions that contributed to the "urban background" of nucleation mode particles throughout a day. On the contrary, it was found that the number concentration of nucleation mode particles was independent of NOx and could be elevated up to 10 times of the "urban background" levels during daytime, suggesting a substantial amount of nucleation mode particles produced from photochemical processes. Averages (± 1σ) of the diameter growth rate (GR) and formation rate of nucleation mode particles, J10, were 11.9 ± 10.6 nm h-1 and 6.9 ± 3.0 cm-3 s-1, respectively. Consistency in the time series of the nucleation mode particle concentration and the proxy of H2SO4 production, UVB · SO2/CS, for new particle formation (NPF) events suggested that photooxidation of SO2 was likely one of the major mechanisms for the formation of new particles in our study area. Moreover, it was revealed that the

  16. Long-term Validation of Cloud-droplet Number Concentration Value Added Product (NDROP VAP) Retrieved from Surface Measurements

    NASA Astrophysics Data System (ADS)

    Lim, K. S. S.; Riihimaki, L.; Comstock, J. M.; Schmid, B.; Sivaraman, C.; Shi, Y.; McFarquhar, G. M.

    2015-12-01

    A new cloud-droplet number concentration (NDROP) Value Added Product (VAP) has been produced at the Atmospheric Radiation Measurement (ARM) Southern Great Plains (SGP) site for the 13 years from January 1998 to January 2011. The droplet number concentration values are retrieved from surface radiometer measurements of cloud optical depth from the multi-filter rotating shadow-band radiometer (MFRSR) and liquid water path from the microwave radiometer (MWR). We validate the NDROP VAP with in situ aircraft measurements from the Cloud and Aerosol Spectrometer probe during the long-term aircraft field campaign, Routine ARM Aerial Facility (AAF) CLOWD Optical Radiative Observations (RACORO). The NDROP VAP considers entrainment effects rather than assuming an adiabatic cloud, which improves the values of the NDROP VAP by reducing the magnitude of cloud-droplet number concentration. The NDROP VAP captures the primary mode of in situ measured droplet number concentration, but produces too wide a distribution due to too frequent high cloud-droplet number concentrations. The large droplet number concentration error corresponds to errors in the MWR retrievals at low liquid water paths due to the limitations of the instrument. Modification of the NDROP VAP through the diagnosed liquid water path, which is constrained by the coordinated solution using cloud optical depth and cloud-droplet effective radius retrievals, alleviates this problem, leading to better agreement with in situ measurements.

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

    EPA Science Inventory

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

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

    NASA Technical Reports Server (NTRS)

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

    2012-01-01

    During the aerosolization process at the sea surface, halides are incorporated into aerosol droplets, where they may play an important role in tropospheric ozone chemistry. Although this process may significantly contribute to the formation of reactive gas phase molecular halogens, little is known about the environmental factors that control how halides selectively accumulate at the air-water interface. In this study, the production of sea spray aerosol is simulated using electrospray ionization (ESI) of 100 nM equimolar solutions of NaCl, NaBr, NaI, NaNO2, NaNO3, NaClO4, and NaIO4. The microdroplets generated are analyzed by mass spectrometry to study the comparative enrichment of anions (f (Isub x-)) and their correlation with ion properties. Although no correlation exists between f (sub x-) and the limiting equivalent ionic conductivity, the correlation coefficient of the linear fit with the size of the anions R(sub x-), dehydration free-energy ?Gdehyd, and polarizability alpha, follows the order: (R(sub x-)(exp -2)) > (R(sub x-)(exp -1)) >(R(sub x-) > delta G(sub dehyd) > alpha. The same pure physical process is observed in H2O and D2O. The factor f (sub x-) does not change with pH (6.8-8.6), counterion (Li+, Na+, K+, and Cs+) substitution effects, or solvent polarity changes in methanol - and ethanol-water mixtures (0 <= xH2O <= 1). Sodium polysorbate 20 surfactant is used to modify the structure of the interface. Despite the observed enrichment of I- on the air-water interface of equimolar solutions, our results of seawater mimic samples agree with a model in which the interfacial composition is increasingly enriched in I- < Br- < Cl- over the oceanic boundary layer due to concentration effects in sea spray aerosol formation.

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

    NASA Astrophysics Data System (ADS)

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

    2009-12-01

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

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

    PubMed

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

    2009-07-01

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

  1. Fluorescent Biological Aerosol Particle Concentrations and Size Distributions Measured with an Ultraviolet Aerodynamic Particle Sizer (UV-APS) in Central Europe

    NASA Astrophysics Data System (ADS)

    Huffman, J. A.; Treutlein, B.; Pöschl, U.

    2009-12-01

    Primary biological aerosol particles (PBAPs), including bacteria, spores and pollen, are essential for the spread of organisms and disease in the biosphere, and numerous studies have suggested that they may be important for atmospheric processes, including the formation of clouds and precipitation. The atmospheric abundance and size distribution of PBAPs, however, are largely unknown. At a semi-urban site in Mainz, Germany, we used an ultraviolet aerodynamic particle sizer (UV-APS) to measure fluorescent biological aerosol particles (FBAPs), which can be regarded as viable bioaerosol particles representing a lower limit for the actual abundance of PBAPs. Fluorescence of non-biological aerosol components are likely to influence the measurement results obtained for fine particles (< 1 µm), but not for coarse particles (1 - 20 µm). Averaged over the four-month measurement period (August - December 2006), the mean number concentration of coarse FBAPs was ~3x10-2 cm-3, corresponding to ~4% of total coarse particle number [1]. The mean mass concentration of FBAPs was ~1 µg m-3, corresponding to ~20% of total coarse particle mass. The FBAP number size distributions exhibited alternating patterns with peaks at various diameters. A pronounced peak at ~3 µm was essentially always observed and can be described by the following campaign-average lognormal fit parameters: geometric mean diameter 3.2 µm, geometric standard deviation 1.3, number concentration 1.6 x 10-2 cm-3. This peak is likely due to fungal spores or agglomerated bacteria, and it exhibited a pronounced diel cycle with maximum intensity during early/mid-morning. FBAP peaks around ~1.5 µm, ~5 µm, and ~13 µm were also observed, but less pronounced and less frequent. These may be explained by single bacterial cells, larger fungal spores, and pollen grains, respectively. The observed number concentrations and characteristic sizes of FBAPs are consistent with microscopic, biological and chemical analyses of

  2. Fluorescent biological aerosol particle concentrations and size distributions measured with an ultraviolet aerodynamic particle sizer (UV-APS) in Central Europe

    NASA Astrophysics Data System (ADS)

    Huffman, J. A.; Treutlein, B.; Pöschl, U.

    2009-08-01

    Primary biological aerosol particles (PBAPs), including bacteria, spores and pollen, are essential for the spread of organisms and disease in the biosphere, and numerous studies have suggested that they may be important for atmospheric processes, including the formation of clouds and precipitation. The atmospheric abundance and size distribution of PBAPs, however, are largely unknown. At a semi-urban site in Mainz, Germany, we used an ultraviolet aerodynamic particle sizer (UV-APS) to measure fluorescent biological aerosol particles (FBAPs), which can be regarded as viable bioaerosol particles representing a lower limit for the actual abundance of PBAPs. Fluorescence of non-biological aerosol components are likely to influence the measurement results obtained for fine particles (<1 μm), but not for coarse particles (1-20 μm). Averaged over the four-month measurement period (August-December 2006), the mean number concentration of coarse FBAPs was ~3×10-2 cm-3, corresponding to ~4% of total coarse particle number. The mean mass concentration of FBAPs was ~1 μg m-3, corresponding to ~20% of total coarse particle mass. The FBAP number size distributions exhibited alternating patterns with peaks at various diameters. A pronounced peak at ~3 μm was essentially always observed and can be described by the following campaign-average lognormal fit parameters: geometric mean diameter 3.2 μm, geometric standard deviation 1.3, number concentration 1.6×10-2 cm-3. This peak is likely due to fungal spores or agglomerated bacteria, and it exhibited a pronounced diel cycle with maximum intensity during early/mid-morning. FBAP peaks around ~1.5 μm, ~5 μm, and ~13 μm were also observed, but less pronounced and less frequent. These may be explained by single bacterial cells, larger fungal spores, and pollen grains, respectively. The observed number concentrations and characteristic sizes of FBAPs are consistent with microscopic, biological and chemical analyses of PBAPs in

  3. Fluorescent biological aerosol particle concentrations and size distributions measured with an Ultraviolet Aerodynamic Particle Sizer (UV-APS) in Central Europe

    NASA Astrophysics Data System (ADS)

    Huffman, J. A.; Treutlein, B.; Pöschl, U.

    2010-04-01

    Primary Biological Aerosol Particles (PBAPs), including bacteria, spores and pollen, are essential for the spread of organisms and disease in the biosphere, and numerous studies have suggested that they may be important for atmospheric processes, including the formation of clouds and precipitation. The atmospheric abundance and size distribution of PBAPs, however, are largely unknown. At a semi-urban site in Mainz, Germany we used an Ultraviolet Aerodynamic Particle Sizer (UV-APS) to measure Fluorescent Biological Aerosol Particles (FBAPs), which provide an estimate of viable bioaerosol particles and can be regarded as an approximate lower limit for the actual abundance of PBAPs. Fluorescence of non-biological aerosol components are likely to influence the measurement results obtained for fine particles (<1 μm), but not for coarse particles (1-20 μm). Averaged over the four-month measurement period (August-December 2006), the mean number concentration of coarse FBAPs was ~3×10-2 cm-3, corresponding to ~4% of total coarse particle number. The mean mass concentration of FBAPs was ~1μg m-3, corresponding to ~20% of total coarse particle mass. The FBAP number size distributions exhibited alternating patterns with peaks at various diameters. A pronounced peak at ~3 μm was essentially always observed and can be described by the following campaign-average lognormal fit parameters: geometric mean diameter 3.2 μm, geometric standard deviation 1.3, number concentration 1.6×10-2 cm-3. This peak is likely due to fungal spores or agglomerated bacteria, and it exhibited a pronounced diel cycle (24-h) with maximum intensity during early/mid-morning. FBAP peaks around ~1.5 μm, ~5 μm, and ~13 μm were also observed, but less pronounced and less frequent. These may be single bacterial cells, larger fungal spores, and pollen grains, respectively. The observed number concentrations and characteristic sizes of FBAPs are consistent with microscopic, biological and chemical

  4. Asian aerosols in North America: Extracting the chemical composition and mass concentration of the Asian continental aerosol plume from long-term aerosol records in the western United States

    NASA Astrophysics Data System (ADS)

    Vancuren, Richard A.

    2003-10-01

    Empirical assessment of the frequency and intensity of dust transport from Asia to North America has found that the dust regularly impacts elevated sites in the western United States, revealing a pattern of consistent, frequent transport above the marine boundary layer. Using the dust as a marker for Asian transport, a subset of Asian-influenced samples was identified within a decade of routine aerosol samples from two sites in the western cordillera of North America: Crater Lake, Oregon, and Mount Lassen, California. This subset was used to guide a statistical analysis to isolate Asian aerosol against the "background" of local contaminants. The analysis was then generalized to all samples during the transport season (March-October) for 1989-1999. A mixture of dust and combustion products dominates the Asian aerosol with typical concentration around 5 μg/m3 and mass median diameter between 2 and 3 μm. Major fine particle (<2.5 μm diameter) constituent fractions are ˜30% mineral, 28% organic compounds, 4% elemental carbon, 10% sulfate, <5% nitrate, and <1% sea salt. A second, possibly Asian, component of aged biomass smoke and sea salt is also present, with typical concentration (when present) around 1.5 μg/m3. Averaged over the transport season the dusty Asian aerosol and the smoky aerosol comprise 60 and 6%, respectively, of total particle mass (<10 μm diameter) and 72 and 13% of fine particle mass at these sites. These data indicate that the Asian continental plume is a significant contributor to aerosol loading at remote high-altitude sites across western North America. This implies a significant influence for Asian emissions on free troposphere aerosols over North America and suggests that they need to be explicitly accounted for in aerosol analyses ranging from climate studies to aerosol regulatory programs.

  5. Using a global aerosol model adjoint to unravel the footprint of spatially-distributed emissions on cloud droplet number and cloud albedo

    NASA Astrophysics Data System (ADS)

    Karydis, V. A.; Capps, S. L.; Moore, R. H.; Russell, A. G.; Henze, D. K.; Nenes, A.

    2012-12-01

    The adjoints of the GEOS-Chem Chemical Transport Model and a comprehensive cloud droplet parameterization are coupled to study the sensitivity of cloud droplet number concentration (Nd) over US regions and Central Europe to global emissions of anthropogenic fine mode aerosol precursors. Simulations reveal that the Nd over the midwestern and southeastern US is mostly sensitive to SO2 emissions during August, and to NH3 emissions during February. Over the western US, Nd is mostly sensitivity to SO2 and primary organic aerosol emissions. In Central Europe, Nd is most sensitive to NH3 and NOx emissions. As expected, local emissions strongly affect Nd; long-range transport, however, is also important for the western US and Europe. Emissions changes projected for the year 2050 are estimated to have the largest impacts on cloud albedo and Nd over Central Europe during August (42% and 82% change, respectively) and western US during February (12% and 36.5% change, respectively).

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

    NASA Astrophysics Data System (ADS)

    Cui, H.; Mao, P.; Zhao, Y.; Nielsen, C. P.; Zhang, J.

    2015-08-01

    China is experiencing severe carbonaceous aerosol pollution driven mainly by large emissions resulting from intensive use of solid fuels. To gain a better understanding of the levels and trends of carbonaceous aerosol emissions and the resulting ambient concentrations at the national scale, we update an emission inventory of anthropogenic organic carbon (OC) and elemental carbon (EC) and employ existing observational studies to analyze characteristics of these aerosols including temporal, spatial, and size distributions, and the levels and shares of secondary organic carbon (SOC) in total OC. We further use ground observations to test the levels and inter-annual trends of the calculated national and provincial emissions of carbonaceous aerosols, and propose possible improvements in emission estimation for the future. The national OC emissions are estimated to have increased 29 % from 2000 (2127 Gg) to 2012 (2749 Gg) and EC by 37 % (from 1356 to 1857 Gg). The residential, industrial, and transportation sectors contributed an estimated 74-78, 17-21, and 4-6 % of the total emissions of OC, respectively, and 49-55, 30-34, and 14-18 % of EC. Updated emission factors (EFs) based on the most recent local field measurements, particularly for biofuel stoves, led to considerably lower emissions of OC compared to previous inventories. Compiling observational data across the country, higher concentrations of OC and EC are found in northern and inland cities, while higher OC / EC ratios are found in southern sites, due to the joint effects of primary emissions and meteorology. Higher OC / EC ratios are estimated at rural and remote sites compared to urban ones, attributed to more emissions of OC from biofuel use, more biogenic emissions of volatile organic compound (VOC) precursors to SOC, and/or transport of aged aerosols. For most sites, higher concentrations of OC, EC, and SOC are observed in colder seasons, while SOC / OC is reduced, particularly at rural and remote sites

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

    NASA Astrophysics Data System (ADS)

    Cui, H.; Mao, P.; Zhao, Y.; Nielsen, C. P.; Zhang, J.

    2015-03-01

    China is experiencing severe carbonaceous aerosol pollution driven mainly by large emissions resulting from intensive use of solid fuels. To gain a better understanding of the levels and trends of carbonaceous aerosol emissions and the resulting ambient concentrations at the national scale, we update an emission inventory of anthropogenic organic carbon (OC) and elemental carbon (EC) and employ existing observational studies to analyze characteristics of these aerosols including temporal, spatial, and size distributions, and the levels and shares of secondary organic carbon (SOC) in total OC. We further use ground observations to test the levels and inter-annual trends of the calculated national and provincial emissions of carbonaceous aerosols, and propose possible improvements in emission estimation for the future. The national OC emissions are estimated to have increased 29% from 2000 (2127 Gg) to 2012 (2749 Gg) and EC by 37% (from 1356 to 1857 Gg). The residential, industrial, and transportation sectors contributed an estimated 76 ± 2, 19 ± 2 and 5 ± 1% of the total emissions of OC, respectively, and 52 ± 3, 32 ± 2 and 16 ± 2% of EC. Updated emission factors based on the most recent local field measurements, particularly for biofuel stoves, lead to considerably lower emissions of OC compared to previous inventories. Compiling observational data across the country, higher concentrations of OC and EC are found in northern and inland cities, while larger OC/EC and SOC/OC ratios are found in southern cities, due to the joint effects of primary emissions and meteorology. Higher SOC/OC ratios are estimated at rural and remote sites compared to urban ones, attributed to more emissions of OC from biofuel use, more biogenic emissions of volatile organic compound (VOC) precursors to SOC, and/or transport of aged aerosols. For most sites, higher concentrations of OC, EC, and SOC are observed in colder seasons, while SOC/OC is reduced, particularly at rural and

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

    NASA Astrophysics Data System (ADS)

    Zhao, Y.

    2015-12-01

    To better understand the levels and trends of carbonaceous aerosol emissions and the resulting ambient concentrations in China, we update an emission inventory of anthropogenic organic carbon (OC) and elemental carbon (EC) and employ existing observational studies to analyze characteristics of these aerosols including temporal and spatial distributions, and the levels and shares of secondary organic carbon (SOC) in total OC. We further use ground observations to test the levels and inter-annual trends of the calculated national and provincial emissions of carbonaceous aerosols. The national OC emissions are estimated to have increased 29% from 2000 (2127 Gg) to 2012 (2749 Gg) and EC by 37% (from 1356 to 1857 Gg). Updated emission factors based on the most recent local field measurements, particularly for biofuel stoves, lead to considerably lower emissions of OC compared to previous inventories. Compiling observational data across the country, higher concentrations of OC and EC are found in northern and inland cities, while SOC/OC ratios are found in southern cities, due to the joint effects of primary emissions and meteorology. Higher OC/EC ratios are estimated at rural and remote sites compared to urban ones, attributed to more emissions of OC from biofuel use, more biogenic emissions of volatile organic compound (VOC) precursors to SOC, and/or transport of aged aerosols. For most sites, smaller SOC/OC is found for cold seasons, particularly at rural and remote sites, attributed partly to weaker atmospheric oxidation and SOC formation in winter. Enhanced SOC formation from oxidization and anthropogenic activities like biomass combustion is judged to have crucial effects on severe haze events characterized by high particle concentrations. Several observational studies indicate an increasing trend in ambient OC/EC (but not in OC or EC individually) from 2000 to 2010, confirming increased atmospheric oxidation of OC across the country. Combining the results of

  9. A numerical simulation of the effect of the number concentration of cloud droplets on Typhoon Chanchu

    NASA Astrophysics Data System (ADS)

    Lin, Wenshi; Xu, Suishan; Sui, C.-H.

    2011-09-01

    In recent years, an increase in the number of anthropogenic aerosol particles has raised the global mean content of aerosol particles in the atmosphere from that of preindustrial times. The indirect effects of aerosols on weather and climate cannot be ignored. In this paper, the fifth generation Pennsylvania State University (PSU)-National Center of Atmospheric Research (NCAR) Nonhydrostatic Mesoscale Model (MM5) is used to simulate Typhoon Chanchu (international designation: 0601), which affected the northwest Pacific. Simulations are conducted in three two-way nested domains with Mercator map projection. The horizontal grid resolutions of the three domains are 27, 9, and 3 km. A period of 60 h is simulated. Surface and rawinsonde conventional observation data and ocean wind data are additionally incorporated into the initialization data. A control (CTL) experiment is run to produce a reasonable forecast. We change the parameter of the cloud condensation nuclei (CCN) concentration (CNP) in the Reisner-2 scheme of the CTL experiment (the default value is 100 cm-3) to conduct two sensitivity experiments. They are the very clean marine (VCM) CNP experiment (CNP = 25 cm-3) and the severe contamination (SC) CNP experiment (CNP = 1,000 cm-3). We investigate the effects of the CNP on Typhoon Chanchu by comparing and analyzing the simulation results of the three experiments in terms of the track, intensity, precipitation, vertical structure, and microphysical processes. The main results show that Typhoon Chanchu slightly weakens as the CNP increases. Increasing the CCN to 1,000 cm-3 results in less graupel, rainwater, and cloud ice but more cloud water. However, the mixing ratio of snow does not distinctly change as the CNP changes. Increasing the CCN leads a rapid decrease in the autoconversion of cloud water to rainwater. There is no autoconversion of cloud water to rainwater in a seriously polluted continental air mass. As the CNP increases, there is more condensation

  10. Particle number concentrations near the Rome-Ciampino city airport

    NASA Astrophysics Data System (ADS)

    Stafoggia, M.; Cattani, G.; Forastiere, F.; Di Menno di Bucchianico, A.; Gaeta, A.; Ancona, C.

    2016-12-01

    Human exposure to ultrafine particles (UFP) has been postulated to be associated with adverse health effects, and there is interest regarding possible measures to reduce primary emissions. One important source of UFP are airport activities, with aircraft take-offs being the most relevant one. We implemented two measurement campaigns of total particle number concentrations (PNC), a proxy for UFP, near a medium-size airport in central Italy. One-minute PNC averages were collected on June 2011 and January 2012 concurrently with 30-min average meteorological data on temperature and wind speed/direction. Data on minute-specific take-offs and landings were obtained by the airport authorities. We applied statistical regression models to relate PNC data to the presence of aircraft activities while adjusting for time trends and meteorology, and estimated the increases in PNC ±15 min before and after take-offs and landings. We repeated the analyses considering prevalent wind direction and by size of the aircraft. We estimated PNC increases of 5400 particles/cm3/minute during the 15 min before and after take-offs, with a peak of 19,000 particles/cm3/minute within 5 min after take-offs. Corresponding figures for landings were 1300 and 1000 particles, respectively. The highest PNC estimates were obtained when the prevailing wind came from the runway direction, and led to estimated PNC increases of 60,000 particles/cm3/minute within 5 min after take-offs. No main differences were noted from the exhaust of different types of aircrafts. The area surrounding Ciampino airport is densely inhabited, raising concerns about the potential adverse effects of long-term and short-term exposure to airport-borne UFP. A close monitoring of airport activities and emissions is mandatory to reduce the public health impact of the airport on the nearby population.

  11. Prediction of particle formation and number concentration over the United States with WRF-Chem + APM model

    NASA Astrophysics Data System (ADS)

    Luo, G.; Yu, F.

    2010-12-01

    Aerosol nucleation events have been widely observed at various locations around the world and well recognized to dominate the particle number abundance and cloud condensation nuclei concentrations in many parts of the troposphere. An advanced particle microphysics model (APM), which has been previously incorporated into a global chemistry transport model (GEOS-Chem) and validated against a large set of aerosol measurements (Yu and Luo, 2009; Yu et al., 2010), has been successfully integrated into the Weather Research and Forecast model coupled with Chemistry (WRF-Chem). The size-resolved (sectional) APM model, which distinguishes secondary and primary particles and keeps track of the amount of secondary species coated on each type of primary particles (black carbon, primary organic carbon, dust, and sea salt), is designed to capture key particle properties important for their health and climatic effects while keep the computing cost at a reasonable level. WRF-Chem has 53 tracers for CBM-Z mechanism, and it took 2.2 hours for one day simulations covering a region of 3780×2916 km2 with 27 km horizontal resolutions and 34 layers on an 8-CPU Linux workstation (2.2 Ghz Dual Quad-Core AMD Opteron Processor 2354). The coupled WRF-Chem-APM model has 138 tracers (85 additional tracers associated with APM), and it took 5.02 hours on the same machine for same day simulation with full size-resolved microphysics (nucleation, condensation, coagulation, deposition, and scavenging) and CBM-Z chemistry. The WRF-Chem + APM has been employed to study the formation and growth of particles over the United States, using relevant outputs from GEOS-Chem + APM as initial conditions and boundary conditions. We show that ion-mediated nucleation of sulfuric acid and water can lead to significant new particle formation over the United States and nucleation rates have strongly spatial and temporal variations. The simulated spatial (both horizontal and vertical) distribution of particle

  12. Impact of atmospheric boundary layer depth variability and wind reversal on the diurnal variability of aerosol concentration at a valley site.

    PubMed

    Pal, S; Lee, T R; Phelps, S; De Wekker, S F J

    2014-10-15

    The development of the atmospheric boundary layer (ABL) plays a key role in affecting the variability of atmospheric constituents such as aerosols, greenhouse gases, water vapor, and ozone. In general, the concentration of any tracers within the ABL varies due to the changes in the mixing volume (i.e. ABL depth). In this study, we investigate the impact on the near-surface aerosol concentration in a valley site of 1) the boundary layer dilution due to vertical mixing and 2) changes in the wind patterns. We use a data set obtained during a 10-day field campaign in which a number of remote sensing and in-situ instruments were deployed, including a ground-based aerosol lidar system for monitoring of the ABL top height (zi), a particle counter to determine the number concentration of aerosol particles at eight different size ranges, and tower-based standard meteorological instruments. Results show a clearly visible decreasing trend of the mean daytime zi from 2900 m AGL (above ground level) to 2200 m AGL during a three-day period which resulted in increased near-surface pollutant concentrations. An inverse relationship exists between the zi and the fine fraction (0.3-0.7 μm) accumulation mode particles (AMP) on some days due to the dilution effect in a well-mixed ABL. These days are characterized by the absence of daytime upvalley winds and the presence of northwesterly synoptic-driven winds. In contrast, on the days with an onset of an upvalley wind circulation after the morning transition, the wind-driven local transport mechanism outweighs the ABL-dilution effect in determining the variability of AMP concentration. The interplay between the ABL depth evolution and the onset of the upvalley wind during the morning transition period significantly governs the air quality in a valley and could be an important component in the studies of mountain meteorology and air quality.

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

    PubMed

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

    2007-01-15

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

  14. Changes in the concentration and composition of anthropogenic and biogenic aerosols in the Finnish Arctic

    NASA Astrophysics Data System (ADS)

    Yli-Tuomi, Tarja

    In this study, historical samples of Arctic haze collected between 1964 and 1978 from northern Finland have been analyzed. The aim has been to determine the sources of the particles, as well as the temporal variation in the source contributions and the source regions. There is no other long-term data available from this early time period and overall, more information about the occurrence, nature, origin and transport of anthropogenic and biogenic aerosols in the European Arctic is needed in order to protect the vulnerable Arctic environment. In addition, evidence for climate/biosphere interaction observed in a previous study of the Arctic aerosol has been sought. The chemical composition data was analyzed with a Multilinear Engine using two different models, pure bilinear and a mixed 2-way/3-way model. The results of receptor modeling were connected with back trajectory data in a Potential Source Contribution Function analysis to determine the likely source areas. Nine sources, namely silver emissions, coal combustion, biomass burning, nonferrous smelters (two sources), crustal elements from remote sources, excess silicon from local sources, sea salt particles and biogenic sulfur emissions from marine algae were found. Although the emissions from industrial areas in the Kola Peninsula have an effect on the concentration of anthropogenic pollutants at Kevo, the highest concentrations during winter are transported from the sources in the mid-latitudes. The yearly strength of the biogenic sulfur emissions showed no dependence on the Northern Hemisphere temperature anomaly and thus, a climatic feedback loop can not be confirmed.

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

    PubMed

    Collier, S; Zhang, Q

    2013-12-17

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

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

    SciTech Connect

    Wang, J.; Cubison, M. J.; Aiken, A. C.; Jimenez, J. L.; Collins, D. R.

    2010-05-01

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

  17. Parameterization and comparative evaluation of the CCN number concentration on Mt. Huang, China

    NASA Astrophysics Data System (ADS)

    Fang, Shasha; Han, Yongxiang; Chen, Kui; Lu, Chunsong; Yin, Yan; Tan, Haobo; Wang, Jin

    2016-11-01

    Quantifying regional CCN concentration is important for reliable estimations of aerosol indirect effects. Based on observational data of the number concentrations of total aerosol (NCN) and cloud condensation nuclei (NCCN), particle number size distribution (PNSD) and, size-resolved activation ratio (SRAR) obtained on Mt. Huang in southeast China from September 19 to October 11, 2012, seven parameterization schemes are used to calculate NCCN employing CCN spectra, bulk activation ratio, cut-off diameter and SRAR. The calculations and the observations are compared and analyzed at four supersaturations (S) from 0.109% to 0.67%. Results show that (1) the parameterization using the average cut-off diameter Dm, which is derived from the various measured PNSD and NCCN, provides the best estimate of NCCN, with coefficient of determination, R2 = 0.70-0.90 and NCCN,cal/NCCN,obs = 0.92-1.11, followed by the method of combining an average size-resolved activation curve with the PNSD, with R2 = 0.71-0.91 and NCCN,cal/NCCN,obs = 0.71-0.91; average D50 together with the PNSD also provides a rational scheme for NCCN prediction, with NCCN,cal/NCCN,obs = 0.86-0.94 and R2 = 0.70-0.89; (2) the method of parameterizing CCN spectra, though straightforward, has limits under polluted conditions. Reasonable NCCN estimate could only be obtained at high S (R2 ≥ 0.85 at S = 0.39% and 0.67%). (3) For the method employing the bulk activation ratio ARB(S), NCCN are substantially overestimated by using total mode-based ARB(S) (NCCN,cal/NCCN,obs = 0.94-1.39, R2 = 0.17-0.67), while applying ammonium sulfate-based ARB(S) yields improved CCN predictions (NCCN,cal/NCCN,obs = 0.91-1.11, R2 = 0.70-0.91). In southern China, when determining the parameterization schemes in climate models, it is first recommended to use the method of average cut-off diameter or SRAR, with the various measured PNSD to predict NCCN. Besides, the method using ammonium sulfate-based ARB(S) and parameterizing CCN spectra

  18. Seasonality of the mass concentration and chemical composition of aerosols around an urbanized basin in East Asia

    NASA Astrophysics Data System (ADS)

    Chou, C. C.-K.; Hsu, W.-C.; Chang, S.-Y.; Chen, W.-N.; Chen, M.-J.; Huang, W.-R.; Huang, S.-H.; Tsai, C.-Y.; Chang, S.-C.; Lee, C.-T.; Liu, S.-C.

    2017-02-01

    This study investigated seasonal variations in the mass concentration and chemical composition of ambient aerosols observed at three stations (coastal, mountainous, and downtown sites) in northern Taiwan from March 2009 to February 2012. The results show that the major aerosol components include ammonium, sulfate, nitrate, sea salt, dust, organic carbon, and elemental carbon, whereas the mass fraction of each species depends on the sampling location and season. A significant correlation (r = 0.7-0.8) was observed in aerosol concentrations measured at the respective stations, indicating that aerosol concentrations were dominated by regional-scale factors. Ammonium, sulfate, and nitrate consistently reached respective peak values in the spring in conjunction with dust particle levels. This shows that the transport of dust and particulate air pollutants from the Asian continent has affected the atmospheric environment in this area. Distinct seasonality was observed for sea salt and secondary organic carbon (SOC): sea salt levels peaked in the autumn, whereas SOC levels peaked in the summer, implying that their sources were regulated by independent seasonal factors. Correlation between sea salt concentration and surface wind speed was derived from coastal measurements and showed a high value for the wind speed sensitivity parameter of around 0.37 for our location. In addition, it was revealed that the SOC concentration in aerosols was positively correlated with oxidant photolysis index (Ox × UVB), suggesting that the SOC seasonality was dominated by hydroxyl radical production.

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

    PubMed

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

    2016-08-10

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

  20. Ozone and aerosol tropospheric concentrations variability analyzed using the ADRIMED measurements and the WRF and CHIMERE models

    NASA Astrophysics Data System (ADS)

    Menut, L.; Mailler, S.; Siour, G.; Bessagnet, B.; Turquety, S.; Rea, G.; Briant, R.; Mallet, M.; Sciare, J.; Formenti, P.; Meleux, F.

    2015-06-01

    During the months of June and July 2013, over the Euro-Mediterranean area, the ADRIMED (Aerosol Direct Radiative Impact on the regional climate in the MEDiterranean region) project was dedicated to characterize the ozone and aerosol concentrations in the troposphere. It is first shown that this period was not highly polluted compared to previous summers in this region, with a moderate ozone production, no significant vegetation fire events and several precipitation periods scavenging the aerosol. The period is modeled with the WRF (Weather Research and Forecasting) and CHIMERE models, and their ability to quantify the observed pollution transport events is presented. The CHIMERE model simulating all kinds of sources (anthropogenic, biogenic, mineral dust, vegetation fires); the aerosol speciation, not available with the measurements, is presented: during the whole period, the aerosol was mainly constituted by mineral dust, sea salt and sulfates close to the surface and mainly by mineral dust in the troposphere. Compared to the AERONET (Aerosol Robotic Network) size distribution, it is shown that the model underestimates the coarse mode near mineral dust sources and overestimates the fine mode in the Mediterranean area, highlighting the need to improve the model representation of the aerosol size distribution both during emissions, long-range transport and deposition.

  1. Relationship between column aerosol optical properties and surface aerosol gravimetric concentrations during the Distributed Regional Aerosol Gridded Observation Network - Northeast ASIA 2012 campaign

    NASA Astrophysics Data System (ADS)

    Jeong, U.; Kim, J.; Seo, S.; Choi, M.; Kim, W. V.; Holben, B. N.; Lee, S.; Kim, J.

    2012-12-01

    One of the main objectives of Distributed Regional Aerosol Gridded Observation Network (DRAGON) campaign in Deriving Information on Surface conditions from Column and Vertically Resolved Observations Relevant to Air Quality (DISCOVER-AQ) mission is to understand the relationship between the column optical properties of the atmosphere and the surface level air quality in terms of aerosols and gases. This study aims to identify the important parameters that affecting the relationship between those variables during the DRAGON - northeast Asia 2012 campaign. Column aerosol optical properties from ten Cimel sun photometers at DRAGON sites in Seoul, MODIS (Moderate Resolution Imaging Spectroradiometer), and GOCI (Geostationary Ocean Color Imager) and particulate matter (PM10) sampling from 40 NIER (National Institute of Environmental Research of South Korea) measurement sites in Seoul during the period of 1st March - 31th May 2012 were employed in this study. The key parameters in relationship between aerosol optical depth (AOD) and PM are reported to be aerosol vertical profile and hygroscopicity of the aerosols. The meteorological conditions including relative humidity, surface temperature, and wind speed that could affect those parameters were investigated.

  2. Saharan dust aerosol over the central Mediterranean Sea: PM10 chemical composition and concentration versus optical columnar measurements

    NASA Astrophysics Data System (ADS)

    Marconi, M.; Sferlazzo, D. M.; Becagli, S.; Bommarito, C.; Calzolai, G.; Chiari, M.; di Sarra, A.; Ghedini, C.; Gómez-Amo, J. L.; Lucarelli, F.; Meloni, D.; Monteleone, F.; Nava, S.; Pace, G.; Piacentino, S.; Rugi, F.; Severi, M.; Traversi, R.; Udisti, R.

    2014-02-01

    This study aims to determine the mineral contribution to PM10 in the central Mediterranean Sea, based on 7 yr of daily PM10 samplings made on the island of Lampedusa (35.5° N, 12.6° E). The chemical composition of the PM10 samples was determined by ion chromatography for the main ions, and, on selected samples, by particle-induced X-ray emission (PIXE) for the total content of crustal markers. Aerosol optical depth measurements were carried out in parallel to the PM10 sampling. The average PM10 concentration at Lampedusa over the period June 2004-December 2010 is 31.5 μg m-3, with low interannual variability. The annual means are below the EU annual standard for PM10, but 9.9% of the total number of daily data exceeds the daily threshold value established by the European Commission for PM (50 μg m-3, European Community, EC/30/1999). The Saharan dust contribution to PM10 was derived by calculating the contribution of Al, Si, Fe, Ti, non-sea-salt (nss) Ca, nssNa, and nssK oxides in samples in which PIXE data were available. Cases in which crustal content exceeded the 75th percentile of the crustal oxide content distribution were identified as elevated dust events. Using this threshold, we obtained 175 events. Fifty-five elevated dust events (31.6%) displayed PM10 higher than 50 μg m-3, with dust contributing by 33% on average. The crustal contribution to PM10 has an annual average value of 5.42 μg m-3, and reaches a value as high as 67.9 μg m-3 (corresponding to 49% of PM10) during an intense Saharan dust event. The crustal content estimated from a single tracer, such as Al or Ca, is in good agreement with the one calculated as the sum of the metal oxides. Conversely, larger crustal contents are derived by applying the EU guidelines for demonstration and subtraction of exceedances in PM10 levels due to high background of natural aerosol. The crustal aerosol amount and contribution to PM10 showed a very small seasonal dependence; conversely, the dust columnar

  3. An Investigation of Size-Dependent Concentration of Trace Elements in Aerosols Emitted from the Oil-Fired Heating Plants

    NASA Technical Reports Server (NTRS)

    Singh, J. J.; Sentell, R. J.; Khandelwal, G. S.

    1976-01-01

    Aerosols emitted from two oil-fired heating plants were aerodynamically separated into eight size groups and were analyzed using the photon-induced X-ray emission (PIXE) technique. It was found that Zn, Mo, Ag, and Pb, and (to a lesser extent) Cd, have a tendency to concentrate preferentially on the smaller aerosols. All of these elements, in certain chemical forms, are known to be toxic. Zinc and molybdenum, although present in low concentrations in the parent fuels, show the strongest tendencies to be concentrated in finer aerosols. Selenium, previously reported to show a very strong tendency to concentration in finer fly ash from coal-fired power plants shows little preference for surface residence. Vanadium, which occurs in significant concentration in the oil fuels for both plants, also shows little preference for surface concentration. Even though the absolute concentrations of the toxic elements involved are well below the safety levels established by the National Institute for Occupational Safety and Health (NIOSH), it would be advisable to raise the heights of the heating-plant exhaust chimneys well above the neighborhood buildings to insure more efficient aerosol dispersal.

  4. Light Absorption in the Stratosphere: Trend, Soot Aerosol Concentration and Contribution by...

    NASA Technical Reports Server (NTRS)

    Pueschel, R. F.; Verma, S.; Strwwa, A. W.; Ferry, G. V.; Hamill, P.; Vay, S.; Gore, Warren J. Y. (Technical Monitor)

    1997-01-01

    The light absorption coefficient, Beta(a) of the stratospheric aerosol is an important quantity that determines its radiative effects. When combined with the aerosol scattering coefficient, Beta(a) it becomes possible to evaluate the aerosol single scatter albedo, omega = Beta(s)/(Beta(s) + Beta(a)) which is essential for modeling the overall radiative effects of the stratospheric aerosol. Pollack1 determined that omega = 0.98 is a critical value that separates stratospheric cooling from warming.

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

    NASA Astrophysics Data System (ADS)

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

    2015-04-01

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

  6. Effects of turbulence on mixed-phase deep convective clouds under different basic-state winds and aerosol concentrations

    NASA Astrophysics Data System (ADS)

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

    2014-12-01

    The effects of turbulence-induced collision enhancement (TICE) on mixed-phase deep convective clouds are numerically investigated using a 2-D cloud model with bin microphysics for uniform and sheared basic-state wind profiles and different aerosol concentrations. Graupel particles account for the most of the cloud mass in all simulation cases. In the uniform basic-state wind cases, graupel particles with moderate sizes account for some of the total graupel mass in the cases with TICE, whereas graupel particles with large sizes account for almost all the total graupel mass in the cases without TICE. This is because the growth of ice crystals into small graupel particles is enhanced due to TICE. The changes in the size distributions of graupel particles due to TICE result in a decrease in the mass-averaged mean terminal velocity of graupel particles. Therefore, the downward flux of graupel mass, and thus the melting of graupel particles, is reduced due to TICE, leading to a decrease in the amount of surface precipitation. Moreover, under the low aerosol concentration, TICE increases the sublimation of ice particles, consequently playing a partial role in reducing the amount of surface precipitation. The effects of TICE are less pronounced in the sheared basic-state wind cases than in the uniform basic-state wind cases because the number of ice crystals is much smaller in the sheared basic-state wind cases than in the uniform basic-state wind cases. Thus, the size distributions of graupel particles in the cases with and without TICE show little difference.

  7. Impacts of alternative fuels in aviation on microphysical aerosol properties and predicted ice nuclei concentration at aircraft cruise altitude

    NASA Astrophysics Data System (ADS)

    Weinzierl, B.; D'Ascoli, E.; Sauer, D. N.; Kim, J.; Scheibe, M.; Schlager, H.; Moore, R.; Anderson, B. E.; Ullrich, R.; Mohler, O.; Hoose, C.

    2015-12-01

    In the past decades air traffic has been substantially growing affecting air quality and climate. According to the International Civil Aviation Authority (ICAO), in the next few years world passenger and freight traffic is expected to increase annually by 6-7% and 4-5%, respectively. One possibility to reduce aviation impacts on the atmosphere and climate might be the replacement of fossil fuels by alternative fuels. However, so far the effects of alternative fuels on particle emissions from aircraft engines and their ability to form contrails remain uncertain. To study the effects of alternative fuels on particle emissions and the formation of contrails, the Alternative Fuel Effects on Contrails and Cruise Emissions (ACCESS) field experiment was conducted in California. In May 2014, the DLR Falcon 20 and the NASA HU-25 jet aircraft were instrumented with an extended aerosol and trace gas payload probing different types of fuels including JP-8 and JP-8 blended with HEFA (Hydroprocessed Esters and Fatty Acids) while the NASA DC8 aircraft acted as the source aircraft for ACCESS-2. Emission measurements were taken in the DC8 exhaust plumes at aircraft cruise level between 9-12 km altitude and at distances between 50 m and 20 km behind the DC8 engines. Here, we will present results from the ACCESS-2 aerosol measurements which show a 30-60% reduction of the non-volatile (mainly black carbon) particle number concentration in the aircraft exhaust for the HEFA-blend compared to conventional JP-8 fuel. Size-resolved particle emission indices show the largest reductions for larger particle sizes suggesting that the HEFA blend contains fewer and smaller black carbon particles. We will combine the airborne measurements with a parameterization of deposition nucleation developed during a number of ice nucleation experiments at the AIDA chamber in Karlsruhe and discuss the impact of alternative fuels on the abundance of potential ice nuclei at cruise conditions.

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

    SciTech Connect

    Allen, H. M.; Draper, D. C.; Ayres, B. R.; Ault, A.; Bondy, A.; Takahama, S.; Modini, R. L.; Baumann, K.; Edgerton, E.; Knote, C.; Laskin, A.; Wang, B.; Fry, J. L.

    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 HNO3 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.

  9. Aerosol Number-size Distributions and Hygroscopic Growth in the Marine Boundary Layer during ACE-Asia

    NASA Astrophysics Data System (ADS)

    Covert, D. S.; Coffman, D. J.; Bates, T. S.

    2001-12-01

    As part of the Aerosol Chemistry Experiment-Asia (ACE-Asia), measurements of the physical and hygroscopic properties of aerosol particles were made on the NOAA Research Vessel Ron Brown in the experiment's study area around southern Japan, the Sea of Japan and the Yellow Sea from 30 March through 19 April, 2001 (Day of Year 90 through 109). The number-size distribution from 3 nm to 10 um diameter was measured with a combination of differential mobility analyzers and aerodynamic particle sizers. The system was operated at 55% relative humidity (RH) for consistency with optical measurements and size dependent chemical sampling on the ship. A separate system consisting of three differential mobility analyzers and humidity conditioners measured the change in hydration of the accumulation mode particles from an initial condition of 55% RH to humidities of 20% and 90% RH. The result is a distribution of hygroscopic growth factors at the end RH relative to the initial humidity. The size distributions varied widely depending on the location of the ship, the source of the air mass and the local meteorological conditions. The dominant features included ultrafine particles (less than 20 nm), soil dust particulate mass (greater than 2 um) and Aitken, accumulation mode number and mass (40 to 600 nm). The results are limited to case studies rather than any statistical or time-space average due to the limited data base and the few sources and air mass types encountered in the 21 day period. The results have been analyzed and categorized according to specific air mass trajectories and chemical analysis and are considered representative of those air masses at the marine boundary layer level. Soil dust dominated distributions were observed on days 101 through 103 with volume concentrations of 50 to 100 um3/cm3 and a volume mean diameter of 3 um. High concentrations of ultrafine particles were observed on the later two of these days from early morning through mid-afternoon in spite

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

    SciTech Connect

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

    2016-10-24

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

  11. Source apportionment of PM2.5 chemically speciated mass and particle number concentrations in New York City

    NASA Astrophysics Data System (ADS)

    Masiol, M.; Hopke, P. K.; Felton, H. D.; Frank, B. P.; Rattigan, O. V.; Wurth, M. J.; LaDuke, G. H.

    2017-01-01

    The major sources of fine particulate matter (PM2.5) in New York City (NYC) were apportioned by applying positive matrix factorization (PMF) to two different sets of particle characteristics: mass concentrations using chemical speciation data and particle number concentrations (PNC) using number size distribution, continuously monitored gases, and PM2.5 data. Post-processing was applied to the PMF results to: (i) match with meteorological data, (ii) use wind data to detect the likely locations of the local sources, and (iii) use concentration weighted trajectory models to assess the strength of potential regional/transboundary sources. Nine sources of PM2.5 mass were apportioned and identified as: secondary ammonium sulfate, secondary ammonium nitrate, road traffic exhaust, crustal dust, fresh sea-salt, aged sea-salt, biomass burning, residual oil/domestic heating and zinc. The sources of PNC were investigated using hourly average number concentrations in six size bins, gaseous air pollutants, mass concentrations of PM2.5, particulate sulfate, OC, and EC. These data were divided into 3 periods indicative of different seasonal conditions. Five sources were resolved for each period: secondary particles, road traffic, NYC background pollution (traffic and oil heating largely in Manhattan), nucleation and O3-rich aerosol. Although traffic does not account for large amounts of PM2.5 mass, it was the main source of particles advected from heavily trafficked zones. The use of residual oil had limited impacts on PM2.5 mass but dominates PNC in cold periods.

  12. How comparable are size-resolved particle number concentrations from different instruments?

    NASA Astrophysics Data System (ADS)

    Hornsby, K. E.; Pryor, S. C.

    2012-12-01

    The need for comparability of particle size resolved measurements originates from multiple drivers including: (i) Recent suggestions that air quality standards for particulate matter should migrate from being mass-based to incorporating number concentrations. This move would necessarily be predicated on measurement comparability which is absolutely critical to compliance determination. (ii) The need to quantify and diagnose causes of variability in nucleation and growth rates in nano-particle experiments conducted in different locations. (iii) Epidemiological research designed to identify key parameters in human health responses to fine particle exposure. Here we present results from a detailed controlled laboratory instrument inter-comparison experiment designed to investigate data comparability in the size range of 2.01-523.3 nm across a range of particle composition, modal diameter and absolute concentration. Particle size distributions were generated using a TSI model 3940 Aerosol Generation System (AGS) diluted using zero air, and sampled using four TSI Scanning Mobility Particle Spectrometer (SMPS) configurations and a TSI model 3091 Fast Mobility Particle Sizer (FMPS). The SMPS configurations used two Electrostatic Classifiers (EC) (model 3080) attached to either a Long DMA (LDMA) (model 3081) or a Nano DMA (NDMA) (model 3085) plumbed to either a TSI model 3025A Butanol Condensed Particle Counting (CPC) or a TSI model 3788 Water CPC. All four systems were run using both high and low flow conditions, and were operated with both the internal diffusion loss and multiple charge corrections turned on. The particle compositions tested were sodium chloride, ammonium nitrate and olive oil diluted in ethanol. Particles of all three were generated at three peak concentration levels (spanning the range observed at our experimental site), and three modal particle diameters. Experimental conditions were maintained for a period of 20 minutes to ensure experimental

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

    NASA Astrophysics Data System (ADS)

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

    2012-08-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2013-01-01

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

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

    NASA Astrophysics Data System (ADS)

    Potter, Lauren E.

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

  16. 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.

  17. Spinning-disk generation and drying of monodisperse solid aerosols with output concentrations sufficient for single-breath inhalation studies.

    PubMed

    Byron, P R; Hickey, A J

    1987-01-01

    The air-driven spinning-disk aerosol generator was modified to allow the production of monodisperse dry spherical aerosols of disodium fluorescein (as model solute) in high output concentrations. Output concentrations were determined by filtration. Optical and aerodynamic size distributions were determined microscopically (after electrostatic precipitation) and by cascade impaction. The generator housing allowed the entrainment of 25-microns primary aqueous solution droplets in a 10-L X min-1 downward flow of dry, filtered air. Internal equipment surfaces were machined flush and polished to minimize aerosol losses. Primary droplets were dried within a stainless steel pipe encased in a tube furnace. Water vapor was removed by diffusion drying. Disk-driven air, satellite droplets, and additional dilution air were vented to waste without using a vacuum. Generator yields were increased by reducing the size of the satellite droplet extraction gap. Aerosols were generated reproducibly by delivering aqueous solutions at a rate of 0.2 mL X min-1 to the center of the disk and spinning at 1000 rps. Dry aerosols, with mass median aerodynamic diameters of 2, 4.9, and 9 microns, were produced in concentrations of 0.89, 5.48, and 54.6 micrograms X L-1 from aqueous solutions containing 0.0374, 0.584, and 3.4% solute by weight. Geometric standard deviations were less than 1.2 in all cases. Concentrations are several times higher than others in the literature and are suitable for single-breath inhalation studies of therapeutic aerosol deposition and effect.

  18. Global Estimates of Average Ground-Level Fine Particulate Matter Concentrations from Satellite-Based Aerosol Optical Depth

    NASA Technical Reports Server (NTRS)

    Van Donkelaar, A.; Martin, R. V.; Brauer, M.; Kahn, R.; Levy, R.; Verduzco, C.; Villeneuve, P.

    2010-01-01

    Exposure to airborne particles can cause acute or chronic respiratory disease and can exacerbate heart disease, some cancers, and other conditions in susceptible populations. Ground stations that monitor fine particulate matter in the air (smaller than 2.5 microns, called PM2.5) are positioned primarily to observe severe pollution events in areas of high population density; coverage is very limited, even in developed countries, and is not well designed to capture long-term, lower-level exposure that is increasingly linked to chronic health effects. In many parts of the developing world, air quality observation is absent entirely. Instruments aboard NASA Earth Observing System satellites, such as the MODerate resolution Imaging Spectroradiometer (MODIS) and the Multi-angle Imaging SpectroRadiometer (MISR), monitor aerosols from space, providing once daily and about once-weekly coverage, respectively. However, these data are only rarely used for health applications, in part because the can retrieve the amount of aerosols only summed over the entire atmospheric column, rather than focusing just on the near-surface component, in the airspace humans actually breathe. In addition, air quality monitoring often includes detailed analysis of particle chemical composition, impossible from space. In this paper, near-surface aerosol concentrations are derived globally from the total-column aerosol amounts retrieved by MODIS and MISR. Here a computer aerosol simulation is used to determine how much of the satellite-retrieved total column aerosol amount is near the surface. The five-year average (2001-2006) global near-surface aerosol concentration shows that World Health Organization Air Quality standards are exceeded over parts of central and eastern Asia for nearly half the year.

  19. Changes in concentration, composition and source contribution of atmospheric organic aerosols by shifting coal to natural gas in Urumqi

    NASA Astrophysics Data System (ADS)

    Ren, Yanqin; Wang, Gehui; Wu, Can; Wang, Jiayuan; Li, Jianjun; Zhang, Lu; Han, Yanni; Liu, Lang; Cao, Cong; Cao, Junji; He, Qing; Liu, Xinchun

    2017-01-01

    Size-segregated aerosols were collected in Urumqi, a megacity in northwest China, during two heating seasons, i.e., before (heating season І: January-March 2012) and after (heating season II: January-March 2014) the project "shifting coal to natural gas", and determined for n-alkanes, PAHs and oxygenated PAHs to investigate the impact of replacement of coal by natural gas on organic aerosols in the urban atmosphere. Our results showed that compared to those in heating season I concentrations of n-alkanes, PAHs and OPAHs decreased by 74%, 74% and 82% in heating season II, respectively. Source apportionment analysis suggested that coal combustion, traffic emission and biomass burning are the major sources of the determined organics during the heating seasons in Urumqi. Traffic emission is the main source for n-alkanes in the city. Coal combustion is the dominant source of PAHs and OPAHs in heating season І, but traffic emission becomes their major source in heating season ІI. Relative contributions of coal combustion to n-alkanes, PAHs and OPAHs in Urumqi decreased from 21 to 75% in heating season I to 4.0-21% in heating season II due to the replacement of coal with natural gas for house heating. Health risk assessment further indicated that compared with that in heating season I the number of lung cancer related to PAHs exposure in Urumqi decreased by 73% during heating season II due to the project implementation. Our results suggest that replacing coal by clean energy sources for house heating will significantly mitigate air pollution and improve human health in China.

  20. [Concentration distribution of metal elements in atmospheric aerosol under different weather conditions in Qingdao Coastal Region].

    PubMed

    Chen, Xiao-Jing; Qi, Jian-Hua; Liu, Ning; Zhang, Xiang-Yu; Shen, Heng-Qing; Liu, Ming-Xu

    2014-10-01

    To know the influence of different weather conditions on the concentration of metal elements in aerosols in the coastal region, total suspended particles (TSP) samples were collected from April to May 2012, and August 2012 to March 2013 in the Qingdao coastal region, and common trace metals were analyzed by using Inductively Coupled Plasma-Mass Spectrometry (ICP-MS) and Inductively Coupled Plasma-Atomic Emission Spectrometry (ICP-AES). The results showed that Al, Ca, Fe, Na, K and Mg were the dominant metal elements in TSP, and the sum of the six elements accounted for 94.2% of the sum of all metals. TSP and metal elements had significant monthly variations, Fe, Al, K, Ca, Mg, Zn, Ba, Mn, Ti, Sr and Li had the highest concentration in November and January, while Be, Sc, Co, Ni and Cr showed the highest value in January. Na had the highest concentration in August, November and February, and the lowest in December. Pb had the highest concentration in January and February, and the lowest in August and December. Enrichment factors indicated that Be, Co, Al, Ca, Fe, K, Mg, Mn, Sr and Ti were mainly affected by natural sources; Li, Cr, Ni, Zn, Ba and Na were affected by natural sources and part of anthropogenic sources; Pb was mainly from anthropogenic sources. Different weather conditions had great impact on TSP and metal elements concentrations, all the measured metals had the highest concentrations in smog except Ti. Compared with the sunny day, the concentration of atmospheric particulate Ti decreased, while the other elements increased by 1 to 4 times in smog. Li, Be, Cr, Ni, Al, Fe, Mg and Mn had little variation in concentration in foggy day, and the concentration of Pb and Na increased considerably. The concentration of Co, Ca and Ti reduced obviously in fog. Except for Cr, Co and Ti, the other elements increased by 1 to 3 times in haze. Most of the elements had the minimal enrichment factors in sunny day, while the other had the maximal enrichment factor in

  1. Technical note: An improved approach to determining background aerosol concentrations with PILS sampling on aircraft

    NASA Astrophysics Data System (ADS)

    Fukami, Christine S.; Sullivan, Amy P.; Ryan Fulgham, S.; Murschell, Trey; Borch, Thomas; Smith, James N.; Farmer, Delphine K.

    2016-07-01

    Particle-into-Liquid Samplers (PILS) have become a standard aerosol collection technique, and are widely used in both ground and aircraft measurements in conjunction with off-line ion chromatography (IC) measurements. Accurate and precise background samples are essential to account for gas-phase components not efficiently removed and any interference in the instrument lines, collection vials or off-line analysis procedures. For aircraft sampling with PILS, backgrounds are typically taken with in-line filters to remove particles prior to sample collection once or twice per flight with more numerous backgrounds taken on the ground. Here, we use data collected during the Front Range Air Pollution and Photochemistry Éxperiment (FRAPPÉ) to demonstrate that not only are multiple background filter samples are essential to attain a representative background, but that the chemical background signals do not follow the Gaussian statistics typically assumed. Instead, the background signals for all chemical components analyzed from 137 background samples (taken from ∼78 total sampling hours over 18 flights) follow a log-normal distribution, meaning that the typical approaches of averaging background samples and/or assuming a Gaussian distribution cause an over-estimation of background samples - and thus an underestimation of sample concentrations. Our approach of deriving backgrounds from the peak of the log-normal distribution results in detection limits of 0.25, 0.32, 3.9, 0.17, 0.75 and 0.57 μg m-3 for sub-micron aerosol nitrate (NO3-), nitrite (NO2-), ammonium (NH4+), sulfate (SO42-), potassium (K+) and calcium (Ca2+), respectively. The difference in backgrounds calculated from assuming a Gaussian distribution versus a log-normal distribution were most extreme for NH4+, resulting in a background that was 1.58× that determined from fitting a log-normal distribution.

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

    NASA Astrophysics Data System (ADS)

    Chan, A. W. H.; Chan, M. N.; Surratt, J. D.; Chhabra, P. S.; Loza, C. L.; Crounse, J. D.; Yee, L. D.; Flagan, R. C.; Wennberg, P. O.; Seinfeld, J. H.

    2010-08-01

    Aldehydes are an important class of products from atmospheric oxidation of hydrocarbons. Isoprene (2-methyl-1,3-butadiene), the most abundantly emitted atmospheric non-methane hydrocarbon, produces a significant amount of secondary organic aerosol (SOA) via methacrolein (a C4-unsaturated aldehyde) under urban high-NOx conditions. Previously, we have identified peroxy methacryloyl nitrate (MPAN) as the important intermediate to isoprene and methacrolein SOA in this NOx regime. Here we show that as a result of this chemistry, NO2 enhances SOA formation from methacrolein and two other α, β-unsaturated aldehydes, specifically acrolein and crotonaldehyde, a NOx effect on SOA formation previously unrecognized. Oligoesters of dihydroxycarboxylic acids and hydroxynitrooxycarboxylic acids are observed to increase with increasing NO2/NO ratio, and previous characterizations are confirmed by both online and offline high-resolution mass spectrometry techniques. Molecular structure also determines the amount of SOA formation, as the SOA mass yields are the highest for aldehydes that are α, β-unsaturated and contain an additional methyl group on the α-carbon. Aerosol formation from 2-methyl-3-buten-2-ol (MBO232) is insignificant, even under high-NO2 conditions, as PAN (peroxy acyl nitrate, RC(O)OONO2) formation is structurally unfavorable. At atmospherically relevant NO2/NO ratios (3-8), the SOA yields from isoprene high-NOx photooxidation are 3 times greater than previously measured at lower NO2/NO ratios. At sufficiently high NO2 concentrations, in systems of α, β-unsaturated aldehydes, SOA formation from subsequent oxidation of products from acyl peroxyl radicals+NO2 can exceed that from RO2+HO2 reactions under the same inorganic seed conditions, making RO2+NO2 an important channel for SOA formation.

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

    NASA Astrophysics Data System (ADS)

    Chan, A. W. H.; Chan, M. N.; Surratt, J. D.; Chhabra, P. S.; Loza, C. L.; Crounse, J. D.; Yee, L. D.; Flagan, R. C.; Wennberg, P. O.; Seinfeld, J. H.

    2010-04-01

    Aldehydes are an important class of products from atmospheric oxidation of hydrocarbons. Isoprene (2-methyl-1,3-butadiene), the most abundantly emitted atmospheric non-methane hydrocarbon, produces a significant amount of secondary organic aerosol (SOA) via methacrolein (a C4-unsaturated aldehyde) under urban high-NOx conditions. Previously, we have identified peroxy methacryloyl nitrate (MPAN) as the important intermediate to isoprene and methacrolein SOA in this NOx regime. Here we show that as a result of this chemistry, NO2 enhances SOA formation from methacrolein and two other α, β-unsaturated aldehydes, specifically acrolein and crotonaldehyde, a NOx effect on SOA formation previously unrecognized. Oligoesters of dihydroxycarboxylic acids and hydroxynitrooxycarboxylic acids are observed to increase with increasing NO2/NO ratio, and previous characterizations are confirmed by both online and offline high-resolution mass spectrometry techniques. Molecular structure also determines the amount of SOA formation, as the SOA mass yields are the highest for aldehydes that are α, β-unsaturated and contain an additional methyl group on the α-carbon. Aerosol formation from 2-methyl-3-buten-2-ol (MBO232) is insignificant, even under high-NO2 conditions, as PAN (peroxy acyl nitrate, RC(O)OONO2) formation is structurally unfavorable. At atmospherically relevant NO2/NO ratios, the SOA yields from isoprene high-NOxphotooxidation are 3 times greater than previously measured at lower NO2/NO ratios. At sufficiently high NO2 concentrations, in systems of α, β-unsaturated aldehydes, SOA formation from subsequent oxidation of products from acyl peroxyl radicals+NO2 can exceed that from RO2+HO2 reactions under the same inorganic seed conditions, making RO2+NO2 an important channel for SOA formation.

  4. Regional and global impacts of Criegee intermediates on atmospheric sulphuric acid concentrations and first steps of aerosol formation.

    PubMed

    Percival, Carl J; Welz, Oliver; Eskola, Arkke J; Savee, John D; Osborn, David L; Topping, David O; Lowe, Douglas; Utembe, Steven R; Bacak, Asan; McFiggans, Gordon; Cooke, Michael C; Xiao, Ping; Archibald, Alexander T; Jenkin, Michael E; Derwent, Richard G; Riipinen, Ilona; Mok, Daniel W K; Lee, Edmond P F; Dyke, John M; Taatjes, Craig A; Shallcross, Dudley E

    2013-01-01

    Carbonyl oxides ("Criegee intermediates"), formed in the ozonolysis of alkenes, are key species in tropospheric oxidation of organic molecules and their decomposition provides a non-photolytic source of OH in the atmosphere (Johnson and Marston, Chem. Soc. Rev., 2008, 37, 699, Harrison et al, Sci, Total Environ., 2006, 360, 5, Gäb et al., Nature, 1985, 316, 535, ref. 1-3). Recently it was shown that small Criegee intermediates, C.I.'s, react far more rapidly with SO2 than typically represented in tropospheric models, (Welz, Science, 2012, 335, 204, ref. 4) which suggested that carbonyl oxides could have a substantial influence on the atmospheric oxidation of SO2. Oxidation of 502 is the main atmospheric source of sulphuric acid (H2SO4), which is a critical contributor to aerosol formation, although questions remain about the fundamental nucleation mechanism (Sipilä et al., Science, 2010, 327, 1243, Metzger et al., Proc. Natl. Acad. Sci. U. S. A., 2010 107, 6646, Kirkby et al., Nature, 2011, 476, 429, ref. 5-7). Non-absorbing atmospheric aerosols, by scattering incoming solar radiation and acting as cloud condensation nuclei, have a cooling effect on climate (Intergovernmental Panel on Climate Change (IPCC), Climate Change 2007: The Physical Science Basis, Cambridge University Press, 2007, ref. 8). Here we explore the effect of the Criegees on atmospheric chemistry, and demonstrate that ozonolysis of alkenes via the reaction of Criegee intermediates potentially has a large impact on atmospheric sulphuric acid concentrations and consequently the first steps in aerosol production. Reactions of Criegee intermediates with SO2 will compete with and in places dominate over the reaction of OH with SO2 (the only other known gas-phase source of H2SO4) in many areas of the Earth's surface. In the case that the products of Criegee intermediate reactions predominantly result in H2SO4 formation, modelled particle nucleation rates can be substantially increased by the improved

  5. Observations of accumulation mode aerosol composition and soot carbon concentrations by means of a high-temperature volatility technique

    NASA Astrophysics Data System (ADS)

    Smith, Michael H.; O'Dowd, Colin D.

    1996-08-01

    A high-temperature volatility system has been deployed for the measurement of the composition and concentration of the accumulation mode aerosol (0.05 μm < r < 1 μm) within the atmospheric boundary layer. This instrumentation comprises a volatility system based around a Particle Measuring Systems ASASP-X optical particle counter, which was operated together with an aethalometer for the direct observation of soot carbon concentrations. By cycling the heater tube through a range of temperatures from near ambient to over 1000°C, size-differentiated information upon aerosol composition may be obtained. Furthermore, by careful selection of analysis temperatures, discrimination is possible between elemental carbon and the more volatile fractions of the soot carbon aerosol. Observations made over the North Sea near the Dutch coast and in the central United Kingdom are presented for differing environmental conditions with soot carbon concentrations ranging from about 100 to over 6000 ng m-3. For polluted conditions over the North Sea the volatility technique clearly showed the dominance of soot carbon particles over other aerosol components with a narrow carbon particle distribution of mode radius around 0.06 μm accounting for about 80% of all particles with radii below 0.1 μm. Under polluted conditions, only about 25% of the total soot carbon aerosol comprised elemental carbon (with the remainder consisting of more volatile material), whereas this proportion rose to around 50% in the lower carbon loadings found in a cleaner maritime air mass. The use of soot carbon loadings as a tracer of anthropogenic aerosol inputs to oceanic regions is explored on the basis of measurements from a NE Atlantic cruise.

  6. International Airport Impacts to Air Quality: Size and Related Properties of Large Increases in Ultrafine Particle Number Concentrations.

    PubMed

    Hudda, N; Fruin, S A

    2016-04-05

    We measured particle size distributions and spatial patterns of particle number (PN) and particle surface area concentrations downwind from the Los Angeles International Airport (LAX) where large increases (over local background) in PN concentrations routinely extended 18 km downwind. These elevations were mostly comprised of ultrafine particles smaller than 40 nm. For a given downwind distance, the greatest increases in PN concentrations, along with the smallest mean sizes, were detected at locations under the landing jet trajectories. The smaller size of particles in the impacted area, as compared to the ambient urban aerosol, increased calculated lung deposition fractions to 0.7-0.8 from 0.5-0.7. A diffusion charging instrument (DiSCMini), that simulates alveolar lung deposition, measured a fivefold increase in alveolar-lung deposited surface area concentrations 2-3 km downwind from the airport (over local background), decreasing steadily to a twofold increase 18 km downwind. These ratios (elevated lung-deposited surface area over background) were lower than the corresponding ratios for elevated PN concentrations, which decreased from tenfold to twofold over the same distance, but the spatial patterns of elevated concentrations were similar. It appears that PN concentration can serve as a nonlinear proxy for lung deposited surface area downwind of major airports.

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

    NASA Astrophysics Data System (ADS)

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

    2011-12-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2012-07-01

    (StD = 4251 cm-3), respectively, and the modal correlations were also investigated. The optical and microphysical parameters, as well as their relationship with each other, are reported. σs correlated strongly with the number concentration of accumulation mode particles and more strongly with the micrometer fraction of particles, but weak correlations were observed for the Aitken and nucleation modes. The origins and pathways of the air masses were examined, and based on sector classification, a relationship between the air mass origin, the optical parameters and the size distributions was established. The low values of the optical and microphysical parameters indicate that the predominant regional aerosol is mostly clean and the shape of the size distribution is characterized by bimodal median size distributions. However, the relationships between the air mass origins and the parameters studied allow us to describe two characteristic situations: the one of the northern and western air masses, which were predominantly composed of marine aerosols and presented the lowest optical and microphysical values observed, indicating predominantly non-absorbent and coarser particles; and the one of the eastern and southern air masses, in which continental aerosols were predominant and exhibited higher values for all parameters, indicating the presence of smaller absorbent particles. The north-northeastern air masses presented the strongest Aitken mode, indicating more recently formed particles, and the southeastern air masses presented the strongest accumulation mode (however, the southeastern air masses were the least common, accounting for only 3% of occurrences).

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

    NASA Astrophysics Data System (ADS)

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

    2015-02-01

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

  10. Study of satellite retrieved aerosol optical depth spatial resolution effect on particulate matter concentration prediction

    NASA Astrophysics Data System (ADS)

    Strandgren, J.; Mei, L.; Vountas, M.; Burrows, J. P.; Lyapustin, A.; Wang, Y.

    2014-10-01

    The Aerosol Optical Depth (AOD) spatial resolution effect is investigated for the linear correlation between satellite retrieved AOD and ground level particulate matter concentrations (PM2.5). The Multi-Angle Implementation of Atmospheric Correction (MAIAC) algorithm was developed for the Moderate Resolution Imaging Spectroradiometer (MODIS) for obtaining AOD with a high spatial resolution of 1 km and provides a good dataset for the study of the AOD spatial resolution effect on the particulate matter concentration prediction. 946 Environmental Protection Agency (EPA) ground monitoring stations across the contiguous US have been used to investigate the linear correlation between AOD and PM2.5 using AOD at different spatial resolutions (1, 3 and 10 km) and for different spatial scales (urban scale, meso-scale and continental scale). The main conclusions are: (1) for both urban, meso- and continental scale the correlation between PM2.5 and AOD increased significantly with increasing spatial resolution of the AOD, (2) the correlation between AOD and PM2.5 decreased significantly as the scale of study region increased for the eastern part of the US while vice versa for the western part of the US, (3) the correlation between PM2.5 and AOD is much more stable and better over the eastern part of the US compared to western part due to the surface characteristics and atmospheric conditions like the fine mode fraction.

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

    NASA Astrophysics Data System (ADS)

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

    2015-04-01

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

  12. Gravity-wave effects on tracer gases and stratospheric aerosol concentrations during the 2013 ChArMEx campaign

    NASA Astrophysics Data System (ADS)

    Chane Ming, Fabrice; Vignelles, Damien; Jegou, Fabrice; Berthet, Gwenael; Renard, Jean-Baptiste; Gheusi, François; Kuleshov, Yuriy

    2016-07-01

    Coupled balloon-borne observations of Light Optical Aerosol Counter (LOAC), M10 meteorological global positioning system (GPS) sondes, ozonesondes, and GPS radio occultation data, are examined to identify gravity-wave (GW)-induced fluctuations on tracer gases and on the vertical distribution of stratospheric aerosol concentrations during the 2013 ChArMEx (Chemistry-Aerosol Mediterranean Experiment) campaign. Observations reveal signatures of GWs with short vertical wavelengths less than 4 km in dynamical parameters and tracer constituents, which are also correlated with the presence of thin layers of strong local enhancements of aerosol concentrations in the upper troposphere and the lower stratosphere. In particular, this is evident from a case study above Ile du Levant (43.02° N, 6.46° E) on 26-29 July 2013. Observations show a strong activity of dominant mesoscale inertia GWs with horizontal and vertical wavelengths of 370-510 km and 2-3 km respectively, and periods of 10-13 h propagating southward at altitudes of 13-20 km during 27-28 July. The European Centre for Medium-Range Weather Forecasts (ECMWF) analyses also show evidence of mesoscale inertia GWs with similar horizontal characteristics above the eastern part of France. Ray-tracing experiments indicate the jet-front system as the main source of observed GWs. Using a simplified linear GW theory, synthetic vertical profiles of dynamical parameters with large stratospheric vertical wind maximum oscillations of ±40 mms-1 are produced for the dominant mesoscale GW observed at heights of 13-20 km. Parcel advection method reveals signatures of GWs in the ozone mixing ratio and the tropospheric-specific humidity. Simulated vertical wind perturbations of the dominant GWs and small-scale perturbations of aerosol concentration (aerosol size of 0.2-0.7 µm) are revealed to be in phase in the lower stratosphere. Present results support the importance of vertical wind perturbations in the GW-aerosol relationship

  13. Opposite seasonality of the aerosol optical depth and the surface particulate matter concentration over the north China Plain

    NASA Astrophysics Data System (ADS)

    Qu, Wenjun; Wang, Jun; Zhang, Xiaoye; Sheng, Lifang; Wang, Wencai

    2016-02-01

    Great difference exists in the aerosol optical depth (AOD) between summer and winter over the North China Plain (NCP). Monthly mean AOD at 550 nm derived from the MODIS (MODerate Resolution Imaging Spectroradiometer) products during 2000-2014 over the area of 30-40° N and 110-125° E exhibits an annual maximum in June (0.855 ± 0.130) and a minimum in December (0.381 ± 0.032). This seasonality of AOD is in the opposite phase with the surface particulate matter (PM) concentration (higher in winter and lower in summer). The possible causes for the higher AOD in June (compared with December) include (a) a higher boundary layer height (BLH) that results in more efficient transport and mixing of aerosol particles to a higher altitude (corresponding to a lower particle concentration near surface) as revealed by the Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observations profile, (b) a higher relative humidity (RH) due to the inshore monsoon circulation that leads to enhancement of aerosol extinction, (c) emission from the regional open stalk burning in the summer harvest season (as seen from MODIS fire products), and (d) the typical eastward open topographical basin over NCP. Under the assumption that the aerosol and water vapor are well mixed within the boundary layer, analysis on multi-year average shows that the differences in BLH, RH and surface PM concentration can explain up to 81% of the variance of monthly averaged AOD over NCP. A preliminarily hypothesis is also suggested to interpret the shift of AOD pattern from winter to summer with an abrupt increase of AOD from May to June, as well as an increase of surface PM2.5 concentration over NCP during the early phase of northward progress of the East Asia summer monsoon front.

  14. Parameterizing cloud condensation nuclei concentrations during HOPE

    NASA Astrophysics Data System (ADS)

    Hande, Luke B.; Engler, Christa; Hoose, Corinna; Tegen, Ina

    2016-09-01

    An aerosol model was used to simulate the generation and transport of aerosols over Germany during the HD(CP)2 Observational Prototype Experiment (HOPE) field campaign of 2013. The aerosol number concentrations and size distributions were evaluated against observations, which shows satisfactory agreement in the magnitude and temporal variability of the main aerosol contributors to cloud condensation nuclei (CCN) concentrations. From the modelled aerosol number concentrations, number concentrations of CCN were calculated as a function of vertical velocity using a comprehensive aerosol activation scheme which takes into account the influence of aerosol chemical and physical properties on CCN formation. There is a large amount of spatial variability in aerosol concentrations; however the resulting CCN concentrations vary significantly less over the domain. Temporal variability is large in both aerosols and CCN. A parameterization of the CCN number concentrations is developed for use in models. The technique involves defining a number of best fit functions to capture the dependence of CCN on vertical velocity at different pressure levels. In this way, aerosol chemical and physical properties as well as thermodynamic conditions are taken into account in the new CCN parameterization. A comparison between the parameterization and the CCN estimates from the model data shows excellent agreement. This parameterization may be used in other regions and time periods with a similar aerosol load; furthermore, the technique demonstrated here may be employed in regions dominated by different aerosol species.

  15. Concentrations and sources of aerosol ions and trace elements during ANTCI-2003

    NASA Astrophysics Data System (ADS)

    Arimoto, R.; Zeng, T.; Davis, D.; Wang, Y.; Khaing, H.; Nesbit, C.; Huey, G.

    As part of the Antarctic Tropospheric Chemistry Investigation (ANTCI), bulk aerosol-particle samples collected at the South Pole were analyzed for nitrate, sulfate, methanesulfonate (MSA), selected trace elements and radionuclides. The samples were collected in the same manner as in the Investigation of Sulfur Chemistry in the Antarctic Troposphere (ISCAT) campaigns of 1998 and 2000. The ANTCI mean sulfate (124 ng m -3) and MSA (9.1 ng m -3) concentrations were comparable to those during ISCAT, but high MSA and sodium and high MSA/sulfate in late November/early December indicated pervasive maritime influences during that time. Trajectory analyses indicate that the Weddell Sea and the Southern Ocean near Wilkes Land were probable sources for the ocean-derived sulfate. The transport of marine air occurs mainly in the buffer layer or free troposphere, and the rapid oxidation of biogenic sulfur to SO 2 appears to be the basis for the observed low MSA/sulfate ratios. Elements typically associated with mineral dust (Al, Fe, K) and other elements with continental sources (Pb, Sb, Zn) had higher concentrations during ANTCI than ISCAT. The mean filterable nitrate (f-NO 3-) concentration (280 ng m -3) also was conspicuously higher than during ISCAT (39 and 150 ng m -3). Several peaks in f-NO 3- were synchronous with those for MSA and sulfate, but some samples had high f-NO 3- but neither high MSA nor sulfate. While there is some evidence that nitrate or nitric acid is transported to SP from distant sources, local emissions of nitrogen oxides from the snow are a far more important source overall.

  16. Comparison of Satellite Observations of Aerosol Optical Depth to Surface Monitor Fine Particle Concentration

    NASA Technical Reports Server (NTRS)

    Kleb, Mary M.; AlSaadi, Jassim A.; Neil, Doreen O.; Pierce, Robert B.; Pippin, Margartet R.; Roell, Marilee M.; Kittaka, Chieko; Szykman, James J.

    2004-01-01

    Under NASA's Earth Science Applications Program, the Infusing satellite Data into Environmental Applications (IDEA) project examined the relationship between satellite observations and surface monitors of air pollutants to facilitate a more capable and integrated observing network. This report provides a comparison of satellite aerosol optical depth to surface monitor fine particle concentration observations for the month of September 2003 at more than 300 individual locations in the continental US. During September 2003, IDEA provided prototype, near real-time data-fusion products to the Environmental Protection Agency (EPA) directed toward improving the accuracy of EPA s next-day Air Quality Index (AQI) forecasts. Researchers from NASA Langley Research Center and EPA used data from the Moderate Resolution Imaging Spectroradiometer (MODIS) instrument combined with EPA ground network data to create a NASA-data-enhanced Forecast Tool. Air quality forecasters used this tool to prepare their forecasts of particle pollution, or particulate matter less than 2.5 microns in diameter (PM2.5), for the next-day AQI. The archived data provide a rich resource for further studies and analysis. The IDEA project uses data sets and models developed for tropospheric chemistry research to assist federal, state, and local agencies in making decisions concerning air quality management to protect public health.

  17. The effect of dry and wet deposition of condensable vapors on secondary organic aerosols concentrations over the continental US

    NASA Astrophysics Data System (ADS)

    Knote, C.; Hodzic, A.; Jimenez, J. L.

    2014-05-01

    The effect of dry and wet deposition of semi-volatile organic compounds (SVOC) in the gas-phase on the concentrations of secondary organic aerosol (SOA) is reassessed using recently derived water solubility information. The water solubility of SVOCs was implemented as a function of their volatility distribution within the regional chemistry transport model WRF-Chem, and simulations were carried out over the continental United States for the year 2010. Results show that including dry and wet removal of gas-phase SVOCs reduces annual average surface concentrations of anthropogenic and biogenic SOA by 48% and 63% respectively over the continental US Dry deposition of gas-phase SVOCs is found to be more effective than wet deposition in reducing SOA concentrations (-40% vs. -8% for anthropogenics, -52% vs. -11% for biogenics). Reductions for biogenic SOA are found to be higher due to the higher water solubility of biogenic SVOCs. The majority of the total mass of SVOC + SOA is actually deposited via the gas-phase (61% for anthropogenics, 76% for biogenics). A number of sensitivity studies shows that this is a robust feature of the modeling system. Other models that do not consider dry and wet removal of gas-phase SVOCs would hence overestimate SOA concentrations by roughly 50%. Assumptions about the water solubility of SVOCs made in some current modeling systems (H* = 105 M atm-1; H* = H* (HNO3)) still lead to an overestimation of 25% / 10% compared to our best estimate. A saturation effect is observed for Henry's law constants above 108 M atm-1, suggesting an upper bound of reductions in surface level SOA concentrations by 60% through removal of gas-phase SVOCs. Considering reactivity of gas-phase SVOCs in the dry deposition scheme was found to be negligible. Further sensitivity studies where we reduce the volatility of organic matter show that consideration of gas-phase SVOC removal still reduces average SOA concentrations by 31% on average. We consider this a lower

  18. Organic aerosol processing in tropical deep convective clouds: Development of a new model (CRM-ORG) and implications for sources of particle number

    NASA Astrophysics Data System (ADS)

    Murphy, B. N.; Julin, J.; Riipinen, I.; Ekman, A. M. L.

    2015-10-01

    The difficulty in assessing interactions between atmospheric particles and clouds is due in part to the chemical complexity of the particles and to the wide range of length and timescales of processes occurring simultaneously during a cloud event. The new Cloud-Resolving Model with Organics (CRM-ORG) addresses these interactions by explicitly predicting the formation, transport, uptake, and re-release of surrogate organic compounds consistent with the volatility basis set framework within a nonhydrostatic, three-dimensional cloud-resolving model. CRM-ORG incorporates photochemical production, explicit condensation/evaporation of organic and inorganic vapors, and a comprehensive set of four different mechanisms describing particle formation from organic vapors and sulfuric acid. We simulate two deep convective cloud events over the Amazon rain forest in March 1998 and compare modeled particle size distributions with airborne observations made during the time period. The model predictions agree well with the observations for Aitken mode particles in the convective outflow (10-14 km) but underpredict nucleation mode particles by a factor of 20. A strong in-cloud particle formation process from organic vapors alone is necessary to reproduce even relatively low ultrafine particle number concentrations (~1500 cm-3). Sensitivity tests with variable initial aerosol loading and initial vertical aerosol profile demonstrate the complexity of particle redistribution and net gain or loss in the cloud. In-cloud particle number concentrations could be enhanced by as much as a factor of 3 over the base case simulation in the cloud outflow but were never reduced by more than a factor of 2 lower than the base. Additional sensitivity cases emphasize the need for constrained estimates of surface tension and affinity of organic vapors to ice surfaces. When temperature-dependent organic surface tension is introduced to the new particle formation mechanisms, the number concentration of

  19. Effects of ice number concentration on dynamics of a shallow mixed-phase stratiform cloud

    SciTech Connect

    Ovchinnikov, Mikhail; Korolev, Alexei; Fan, Jiwen

    2011-09-17

    Previous modeling studies have shown a high sensitivity of simulated properties of mixed-phase clouds to ice number concentration, Ni, with many models losing their ability to maintain the liquid phase as Ni increases. Although models differ widely at what Ni the mixed-phase cloud becomes unstable, the transition from a mixed-phase to an ice only cloud in many cases occurs over a narrow range of ice concentration. To gain better understanding of this non-linear model behavior, in this study, we analyze simulations of a mixed-phase stratiform Artic cloud observed on 26 April 2008 during recent Indirect and Semi-Direct Aerosol Campaign (ISDAC). The BASE simulation, in which Ni is constrained to match the measured value, produces a long-lived cloud in a quasi steady state similar to that observed. The simulation without the ice (NO_ICE) produces a comparable but slightly thicker cloud because more moisture is kept in the mixed layer due to lack of precipitation. When Ni is quadrupled relative to BASE (HI_ICE), the cloud starts loosing liquid water almost immediately and the liquid water path is reduced by half in less than two hours. The changes in liquid water are accompanied by corresponding reduction in the radiative cooling of the layer and a slow down in the vertical mixing, confirming the important role of interactions among microphysics, radiation and dynamics in this type of clouds. Deviations of BASE and HI_ICE from NO_ICE are used to explore the linearity of the model response to variation in Ni. It is shown that at early stages, changes in liquid and ice water as well as in radiative cooling/heating rates are proportional to the Ni change, while changes in the vertical buoyancy flux are qualitatively different in HI_ICE compared to BASE. Thus, while the positive feedback between the liquid water path and radiative cooling of the cloud layer is essential for glaciation of the cloud at higher Ni, the non-linear (with respect to Ni) reduction in positive

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

    NASA Astrophysics Data System (ADS)

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

    2016-09-01

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

  1. Synergistic interaction of ozone and respirable aerosols on rat lungs. II. Synergy between ammonium sulfate aerosol and various concentrations of ozone

    SciTech Connect

    Warren, D.L.; Guth, D.J.; Last, J.A.

    1986-07-01

    Pulmonary responses after continuous exposure of rats to concentrations of ozone (O3) ranging from 0.12 to 0.64 ppm were quantified by measuring tissue collagen synthesis rate, tissue protein and DNA content, and various constituents of bronchoalveolar lavage fluid. After 7 days of exposure to 0.64 ppm of O3, lung collagen synthesis rate and tissue content of protein and DNA were elevated. After shorter durations of exposure to 0.64 ppm of O3, significant elevations were observed in the protein content and the activities of lactate dehydrogenase, acid phosphatase, and N-acetyl-beta-D-glucosaminidase from lavage fluid. After exposure of rats to 0.20 ppm of O3 for 7 days, changes could be detected in both lung collagen synthesis rate and tissue protein content. Total lavagable protein content, a sensitive indicator for O3-induced effects upon the lung, was significantly elevated in lungs of rats exposed to 0.12 or 0.20 ppm of O3. To examine whether a synergistic interaction occurred between 0.20 or 0.64 ppm of O3 and acid aerosols, rats were continuously exposed to O3 with and without concurrent exposure to 5 mg/m3 of ammonium sulfate. A synergistic interaction between 0.20 ppm of O3 and ammonium sulfate aerosol was observed by measurement of total lavagable protein and of lung collagen synthesis rate. These results demonstrate that ammonium sulfate aerosol interacts synergistically with O3 at concentrations of O3 that approach ambient levels.

  2. A method for retrieving vertical distribution of aerosol mass concentration in atmosphere from results of lidar sensing at Nd:YAG laser wavelengths

    NASA Astrophysics Data System (ADS)

    Lisenko, S. A.; Kugeiko, M. M.

    2011-03-01

    A method for retrieving the vertical profiles of atmospheric aerosol concentration from the results of lidar sensing at Ng:YAG laser wavelengths is developed based on the found multiple regressions between the optical location characteristics of aerosol at wavelengths of 0.355, 0.532, and 1.064 nm, as well as between the aerosol backscattering coefficient at these wavelengths and the concentration of aerosol particles. The method does not require solving ill-posed inverse problems and minimizes the use of a priori information. The reliability and generality of regressions obtained are confirmed by their good agreement with the AERO-NET data. The method efficiency is demonstrated by numerical experiments on retrieving profiles of back-scattering coefficients and concentration that corresponds to different optical models of aerosol.

  3. Comparison of POLDER Derived Aerosol Optical Thickness to Surface Monitor Fine Particle Concentration

    NASA Astrophysics Data System (ADS)

    Leon, J.; Kacenelenbogen, M.; Chiapello, I.

    2005-12-01

    The Particulate Matter (PM) mass measured at the ground level is a common way to quantify the amount of aerosol particles in the atmosphere and is used as a standard to evaluate air quality. Satellite remote sensing is well suited for a daily monitoring of the aerosol load. However, there are no straightforward relationship between aerosol optical properties derived from the satellite sensor and the PM mass at the ground. This paper is focused on the use of Polarization and Directionality of Earth's Reflectance (POLDER-2) derived aerosol optical thickness (AOT) for the monitoring of PM2.5. We present a correlation study between PM2.5 data collected in the frame of the French Environmental protection agency, aerosol optical properties derived from Sun photometer measurements, and POLDER derived-AOT over the land. POLDER AOT retrieval algorithm over the land is based on the use of the measurement of the linear polarized light in the 670 nm and 865 nm channels. We show that only the fine fraction (below 0.3 μm) of the aerosol size distribution contributes to the signal in polarization and then to the POLDER derived-AOT and then is well suited for monitoring of fine particle. The correlation between POLDER AOT and PM2.5 is significant (R between 0.6 and 0.7) over several sites. We present a tentative evaluation of Air Quality Categories from satellite data.

  4. Aerosol Observing System (AOS) Handbook

    SciTech Connect

    Jefferson, A

    2011-01-17

    The Aerosol Observing System (AOS) is a suite of in situ surface measurements of aerosol optical and cloud-forming properties. The instruments measure aerosol properties that influence the earth’s radiative balance. The primary optical measurements are those of the aerosol scattering and absorption coefficients as a function of particle size and radiation wavelength and cloud condensation nuclei (CCN) measurements as a function of percent supersaturation. Additional measurements include those of the particle number concentration and scattering hygroscopic growth. Aerosol optical measurements are useful for calculating parameters used in radiative forcing calculations such as the aerosol single-scattering albedo, asymmetry parameter, mass scattering efficiency, and hygroscopic growth. CCN measurements are important in cloud microphysical models to predict droplet formation.

  5. Concentrations of iodine isotopes ((129)I and (127)I) and their isotopic ratios in aerosol samples from Northern Germany.

    PubMed

    Daraoui, A; Riebe, B; Walther, C; Wershofen, H; Schlosser, C; Vockenhuber, C; Synal, H-A

    2016-04-01

    New data about (129)I, (127)I concentrations and their isotopic ratios in aerosol samples from the trace survey station of the Physikalisch-Technische Bundesanstalt (PTB) in Braunschweig, Northern Germany, are presented and discussed in this paper. The investigated samples were collected on a weekly basis during the years 2011 to 2013. Iodine was extracted from aerosol filters using a strong basic solution and was separated from the matrix elements with chloroform and was analysed by accelerator mass spectrometry (AMS) for (129)I and by inductively coupled plasma mass spectrometry (ICP-MS) for (127)I. The concentrations of (127)I and (129)I in aerosol filters ranged from 0.31 to 3.71 ng m(-3) and from 0.06 to 0.75 fg m(-3), respectively. The results of (129)I/(127)I isotopic ratios were in the order 10(-8) to 10(-7). The (129)I originated directly from gaseous emissions and indirectly from liquid emissions (via sea spray) from the reprocessing plants in Sellafield and La Hague. In comparison with the results of (131)I after the Fukushima accident, no contribution of (129)I from this accident was detectable in Central Europe due to the high background originating from the (129)I releases of the European reprocessing plants. (129)I atmospheric activity concentrations were compared with those of an anthropogenic radionuclide ((85)Kr). We did not find any correlation between (129)I and (85)Kr, both having nuclear reprocessing plant as the main source.

  6. n-Alkanoic monocarboxylic acid concentrations in urban and rural aerosols: Seasonal dependence and major sources

    NASA Astrophysics Data System (ADS)

    Shannigrahi, Ardhendu S.; Pettersson, Jan B. C.; Langer, Sarka; Arrhenius, Karine; Hagström, Magnus; Janhäll, Sara; Hallquist, Mattias; Pathak, Ravi Kant

    2014-06-01

    We report new data on the abundance and distribution of n-monocarboxylic acids (n-MCAs) in fine- and coarse-mode aerosols in rural and urban areas of Sweden, and determine their possible sources. Overall, C6-C16n-MCAs accounted for ~ 0.5-1.2% of the total PM10 (particulate matter ≤ 10 μm) mass. In general, the C12-C16 fraction was the most abundant (> 75%), with the exception of wintertime samples from a rural site, where C6-C11 acids accounted for 65% of the total C6-C16n-MCA mass. Positive matrix factorization analysis revealed four major sources of n-MCAs: traffic emissions, wood combustion, microbial activity, and a fourth factor that was dominated by semi-volatile n-MCAs. Traffic emissions were important in the urban environment in both seasons and at the rural site during winters, and were a major source of C9-C11 acids. Wood combustion was a significant source at urban sites during the winter and also to some extent at the rural site in both seasons. This is consistent with the use of wood for domestic heating but may also be related to meat cooking. Thus, during the winter, traffic, wood combustion and microbial activity were all important sources in the urban environment, while traffic was the dominant source at the rural site. During the summer, there was considerable day-to-day variation in n-MCA concentrations but microbial activity was the dominant source. The semi-volatile low molecular weight C6-C8 acids accounted for a small (~ 5-10%) fraction of the total mass of n-MCAs. This factor is unlikely to be linked to a single source and its influence instead reflects the partitioning of these compounds between the gas and particle phases. This would explain their greater contribution during the winter.

  7. Vertical profile of elemental concentrations in aerosol particles in the Bermuda area during GCE/CASE/WATOX

    NASA Astrophysics Data System (ADS)

    Ennis, G.; Sievering, H.

    1990-06-01

    During the 1988 Global Change Expedition/Coordinated Air-Sea Experiment/Western Atlantic Ocean Experiment (GCE/CASE/WATOX) joint effort, research was conducted to determine elemental concentrations in atmospheric aerosol particles near Bermuda, to construct a three-level (15, 150, and 2600 m ASL) vertical profile of these concentrations, and to ascertain the source of the particles. Samples were collected by the NOAA King Air aircraft and NOAA ship Mt. Mitchell on July 24-28, 1988. Concentration determinations were made for 16 elements through the use of an X ray fluorescence instrument designed for analysis of small-mass samples. A layering effect was found; concentrations of several elements at 150 m were more than twice their respective concentrations at 15 m and 2600 m. Enrichment factors, V/Mn ratio, and correlations between concentrations suggest a Saharan mineral source, despite air mass back trajectories that show no direct continental input for up to 10 days prior to sample collection. Estimated total mineral aerosol concentrations at 15 m, 150 m, and 2600 m are 1.5, 4.1, and 2.1 μg m-3.

  8. Diurnal and seasonal variations of meteorology and aerosol concentrations in the foothills of the nepal himalayas (Nagarkot: 1,900 m asl)

    NASA Astrophysics Data System (ADS)

    Shrestha, Rudra K.; Gallagher, Martin W.; Connolly, Paul J.

    2016-02-01

    A 10-months long monitoring experiment to investigate the diurnal and seasonal variation of aerosol size distribution at Nagarkot (1,900 m asl) in the Kathmadu Valley was carried out as part of a study on katabatic and anabatic influence on pollution dispersion mechanisms. Seasonal means show total aerosol number concentration was highest during post-monsoon season (775 ± 417 cm-3) followed by pre-monsoon (644 ± 429 cm-3) and monsoon (293 ± 205 cm-3) periods. Fine particle concentration (0.25 μm ≤ DP ≤ 2.5 μm) dominated in all seasons, however, contribution by coarse particles (3.0 μm ≤ DP ≤ 10.0 μm) is more significant in the monsoon season with contributions from particles larger than 10.0 μm being negligible. Our results show a regular diurnal pattern of aerosol concentration in the valley with a morning and an evening peak. The daily twin peaks are attributed to calm conditions followed by transitional growth and break down of the valley boundary layer below. The peaks are generally associated with enhancement of the coarse particle fraction. The evening peak is generally higher than the morning peak, and is caused by fresh evening pollution from the valley associated with increased local activities coupled with recirculation of these trapped pollutants. Relatively clean air masses from neighbouring valleys contribute to the smaller morning peak. Gap flows through the western passes of the Kathmandu Valley, which sweep away the valley pollutants towards the eastern passes modulated by the mountain - valley wind system, are mainly responsible for the dominant pollutant circulation patterns exhibited within the valley.

  9. Aerosol effects on deep convective clouds: impact of changes in aerosol size distribution and aerosol activation parameterization

    NASA Astrophysics Data System (ADS)

    Ekman, A. M. L.; Engström, A.; Söderberg, A.

    2010-03-01

    A cloud-resolving model including explicit aerosol physics and chemistry is used to study the impact of aerosols on deep convective strength. More specifically, by conducting six sensitivity series we examine how the complexity of the aerosol model, the size of the aerosols and the aerosol activation parameterization influence the aerosol-induced deep convective cloud sensitivity. Only aerosol effects on liquid droplet formation are considered. We find that an increased aerosol concentration generally results in stronger convection, which for the simulated case is in agreement with the conceptual model presented by Rosenfeld et al. (2008). However, there are two sensitivity series that do not display a monotonic increase in updraft velocity with increasing aerosol concentration. These exceptions illustrate the need to: 1) account for changes in evaporation processes and subsequent cooling when assessing aerosol effects on deep convective strength, 2) better understand graupel impaction scavenging of aerosols which may limit the number of CCN at a critical stage of cloud development and thereby dampen the convection, 3) increase our knowledge of aerosol recycling due to evaporation of cloud droplets. Furthermore, we find a significant difference in the aerosol-induced deep convective cloud sensitivity when using different complexities of the aerosol model and different aerosol activation parameterizations. For the simulated case, a 100% increase in aerosol concentration results in a difference in average updraft between the various sensitivity series which is as large as the average updraft increase itself. The model simulations also show that the change in graupel and rain formation is not necessarily directly proportional to the change in updraft velocity. For example, several of the sensitivity series display a decrease of the rain amount at the lowest model level with increasing updraft velocity. Finally, an increased number of aerosols in the Aitken mode (here

  10. [Ultrafine particle number concentration and size distribution of vehicle exhaust ultrafine particles].

    PubMed

    Lu, Ye-qiang; Chen, Qiu-fang; Sun, Zai; Cai, Zhi-liang; Yang, Wen-jun

    2014-09-01

    Ultrafine particle (UFP) number concentrations obtained from three different vehicles were measured using fast mobility particle sizer (FMPS) and automobile exhaust gas analyzer. UFP number concentration and size distribution were studied at different idle driving speeds. The results showed that at a low idle speed of 800 rmin-1 , the emission particle number concentration was the lowest and showed a increasing trend with the increase of idle speed. The majority of exhaust particles were in Nuclear mode and Aitken mode. The peak sizes were dominated by 10 nm and 50 nm. Particle number concentration showed a significantly sharp increase during the vehicle acceleration process, and was then kept stable when the speed was stable. In the range of 0. 4 m axial distance from the end of the exhaust pipe, the particle number concentration decayed rapidly after dilution, but it was not obvious in the range of 0. 4-1 m. The number concentration was larger than the background concentration. Concentration of exhaust emissions such as CO, HC and NO showed a reducing trend with the increase of idle speed,which was in contrast to the emission trend of particle number concentration.

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

    PubMed Central

    Ramana, M. V.; Devi, Archana

    2016-01-01

    Significant quantities of carbon soot aerosols are emitted into pristine parts of the atmosphere by marine shipping. Soot impacts the radiative balance of the Earth-atmosphere system by absorbing solar-terrestrial radiation and modifies the microphysical properties of clouds. Here we examined the impact of black carbon (BC) on net warming during monsoon season over southern Bay-of-Bengal, using surface and satellite measurements of aerosol plumes from shipping. Shipping plumes had enhanced the BC concentrations by a factor of four around the shipping lane and exerted a strong positive influence on net warming. Compiling all the data, we show that BC atmospheric heating rates for relatively-clean and polluted-shipping corridor locations to be 0.06 and 0.16 K/day respectively within the surface layer. Emissions from maritime ships had directly heated the lower troposphere by two-and-half times and created a gradient of around 0.1 K/day on either side of the shipping corridor. Furthermore, we show that ship emitted aerosol plumes were responsible for increase in the concentration of cloud condensation nuclei (CCN) by an order of magnitude that of clean air. The effects seen here may have significant impact on the monsoonal activity over Bay-of-Bengal and implications for climate change mitigation strategies. PMID:27480275

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

    NASA Astrophysics Data System (ADS)

    Ramana, M. V.; Devi, Archana

    2016-08-01

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

  13. 40 CFR Table F-5 to Subpart F of... - Estimated Mass Concentration Measurement of PM 2.5 for Idealized “Typical” Coarse Aerosol Size...

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 6 2013-07-01 2013-07-01 false Estimated Mass Concentration... 53—Estimated Mass Concentration Measurement of PM 2.5 for Idealized “Typical” Coarse Aerosol Size... Concentration (µg/m 3) Estimated Mass Concentration Measurement (µg/m 3) Ideal Sampler Fractional...

  14. 40 CFR Table F-5 to Subpart F of... - Estimated Mass Concentration Measurement of PM2.5 for Idealized “Typical” Coarse Aerosol Size...

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 6 2012-07-01 2012-07-01 false Estimated Mass Concentration... 53—Estimated Mass Concentration Measurement of PM2.5 for Idealized “Typical” Coarse Aerosol Size... Concentration (µg/m3) Estimated Mass Concentration Measurement (µg/m3) Ideal Sampler Fractional...

  15. 40 CFR Table F-5 to Subpart F of... - Estimated Mass Concentration Measurement of PM 2.5 for Idealized “Typical” Coarse Aerosol Size...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 6 2014-07-01 2014-07-01 false Estimated Mass Concentration... 53—Estimated Mass Concentration Measurement of PM 2.5 for Idealized “Typical” Coarse Aerosol Size... Concentration (µg/m3) Estimated Mass Concentration Measurement (µg/m3) Ideal Sampler Fractional...

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

    NASA Astrophysics Data System (ADS)

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

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

  17. Evaluation of long-term surface-retrieved cloud droplet number concentration with in situ aircraft observations: ARM Cloud Droplet Number Concentration

    SciTech Connect

    Lim, Kyo-Sun Sunny; Riihimaki, Laura; Comstock, Jennifer M.; Schmid, Beat; Sivaraman, Chitra; Shi, Yan; McFarquhar, Greg M.

    2016-03-06

    A new cloud-droplet number concentration (NDROP) value added product (VAP) has been produced at the Atmospheric Radiation Measurement (ARM) Southern Great Plains (SGP) site for the 13 years from January 1998 to January 2011. The retrieval is based on surface radiometer measurements of cloud optical depth from the multi-filter rotating shadow-band radiometer (MFRSR) and liquid water path from the microwave radiometer (MWR). It is only applicable for single-layered warm clouds. Validation with in situ aircraft measurements during the extended-term aircraft field campaign, Routine ARM Aerial Facility (AAF) CLOWD Optical Radiative Observations (RACORO), shows that the NDROP VAP robustly reproduces the primary mode of the in situ measured probability density function (PDF), but produces a too wide distribution, primarily caused by frequent high cloud-droplet number concentration. Our analysis shows that the error in the MWR retrievals at low liquid water paths is one possible reason for this deficiency. Modification through the diagnosed liquid water path from the coordinate solution improves not only the PDF of the NDROP VAP but also the relationship between the cloud-droplet number concentration and cloud-droplet effective radius. Consideration of entrainment effects rather than assuming an adiabatic cloud improves the values of the NDROP retrieval by reducing the magnitude of cloud-droplet number concentration. Aircraft measurements and retrieval comparisons suggest that retrieving the vertical distribution of cloud-droplet number concentration and effective radius is feasible with an improvement of the parameter representing the mixing effects between environment and clouds and with a better understanding of the effect of mixing degree on cloud properties.

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

    NASA Astrophysics Data System (ADS)

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

    2016-06-01

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

  19. Explicit Simulation of Aerosol Physics in a Cloud-Resolving Model: Aerosol Transport and Processing in the Free Troposphere.

    NASA Astrophysics Data System (ADS)

    Ekman, Annica M. L.; Wang, Chien; Ström, Johan; Krejci, Radovan

    2006-02-01

    Large concentrations of small aerosols have been previously observed in the vicinity of anvils of convective clouds. A 3D cloud-resolving model (CRM) including an explicit size-resolving aerosol module has been used to examine the origin of these aerosols. Five different types of aerosols are considered: nucleation mode sulfate aerosols (here defined by 0 d 5.84 nm), Aitken mode sulfate aerosols (here defined by 5.84 nm d 31.0 nm), accumulation mode sulfate aerosols (here defined by d 31.0 nm), mixed aerosols, and black carbon aerosols.The model results suggest that approximately 10% of the initial boundary layer number concentration of Aitken mode aerosols and black carbon aerosols are present at the top of the convective cloud as the cloud reaches its decaying state. The simulated average number concentration of Aitken mode aerosols in the cloud anvil (1.6 × 104 cm-3) is in the same order of magnitude as observations. Thus, the model results strongly suggest that vertical convective transport, particularly during the active period of the convection, is responsible for a major part of the appearance of high concentrations of small aerosols (corresponding to the Aitken mode in the model) observed in the vicinity of cloud anvils.There is some formation of new aerosols within the cloud, but the formation is small. Nucleation mode aerosols are also efficiently scavenged through impaction scavenging by precipitation. Accumulation mode and mixed mode aerosols are efficiently scavenged through nucleation scavenging and their concentrations in the cloud anvil are either very low (mixed mode) or practically zero (accumulation mode).In addition to the 3D CRM, a box model, including important features of the aerosol module of the 3D model, has been used to study the formation of new aerosols after the cloud has evaporated. The possibility of these aerosols to grow to suitable cloud condensation or ice nuclei size is also examined. Concentrations of nucleation mode aerosols

  20. Solar concentration properties of flat fresnel lenses with large F-numbers

    NASA Technical Reports Server (NTRS)

    Cosby, R. M.

    1978-01-01

    The solar concentration performances of flat, line-focusing sun-tracking Fresnel lenses with selected f-numbers between 0.9 and 2.0 were analyzed. Lens transmittance was found to have a weak dependence on f-number, with a 2% increase occuring as the f-number is increased from 0.9 to 2.0. The geometric concentration ratio for perfectly tracking lenses peaked for an f-number near 1.35. Intensity profiles were more uniform over the image extent for large f-number lenses when compared to the f/0.9 lens results. Substantial decreases in geometri concentration ratios were observed for transverse tracking errors equal to or below 1 degree for all f-number lenses. With respect to tracking errors, the solar performance is optimum for f-numbers between 1.25 and 1.5.

  1. Influence of atmospheric dispersion and new particle formation events on ambient particle number concentration in Rochester, United States, and Toronto, Canada.

    PubMed

    Jeong, Cheol-Heon; Evans, Greg J; Hopke, Philip K; Chalupa, David; Utell, Mark J

    2006-04-01

    Continuous measurements of particle number concentrations were performed in Rochester, NY, and Toronto, Ontario, Canada during the 2003 calendar year. Strong seasonal dependency in particle number concentration was observed at two sites. The average number concentration of ambient particles was 9670 +/- 6960 cm(-3) in Rochester, whereas in Toronto the average number of particles was 28,010 +/- 13,350 cm(-3). The particle number concentrations were higher in winter months than in summer months by a factor of 1.5 in Rochester and 1.6 in Toronto. In general, there were also distinct diurnal variations of aerosol number concentration. The highest weekdays/weekends ratio of number concentration was typically observed during the rush-hour period in winter months with a ratio of 2.1 in Rochester and 2.0 in Toronto. The correlation in the total particle number concentrations between the two urban sites was stronger in winter because of the common urban traffic patterns, but weaker in summer because of local sulfur dioxide (SO2)-related particle formation events in Rochester in the summer. Strong morning particle formation events were frequently observed during colder winter months. Good correlations between particle number and carbon monoxide (CO) as well as temperature suggested that motorvehicle emissions lead to the formation of new particles as the exhaust mixes with the cold air. Regional nucleation and growth events frequently occurred in April. Local SO2-related particle formation events most frequently occurred in August. SO2 and UV-B were highly correlated with particle concentration, suggesting a high association of photochemical processes with these local events. A high directionality in a northerly direction was observed for particle number and SO2, indicating the influence of point sources located north of Rochester.

  2. Trace Gas/Aerosol Boundary Concentrations and their Impacts on Continental-scale AQMEII Modelling Domains

    EPA Science Inventory

    Over twenty modeling groups are participating in the Air Quality Model Evaluation International Initiative (AQMEII) in which a variety of mesoscale photochemical and aerosol air quality modeling systems are being applied to continental-scale domains in North America and Europe fo...

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

    NASA Astrophysics Data System (ADS)

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

    2015-12-01

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

  4. Studying the concentration dependence of the aggregation number of a micellar model system by SANS.

    PubMed

    Amann, Matthias; Willner, Lutz; Stellbrink, Jörg; Radulescu, Aurel; Richter, Dieter

    2015-06-07

    We present a small-angle neutron scattering (SANS) structural characterization of n-alkyl-PEO polymer micelles in aqueous solution with special focus on the dependence of the micellar aggregation number on increasing concentration. The single micellar properties in the dilute region up to the overlap concentration ϕ* are determined by exploiting the well characterized unimer exchange kinetics of the model system in a freezing and diluting experiment. The micellar solutions are brought to thermodynamic equilibrium at high temperatures, where unimer exchange is fast, and are then cooled to low temperatures and diluted to concentrations in the limit of infinite dilution. At low temperatures the kinetics, and therefore the key mechanism for micellar rearrangement, is frozen on the experimental time scale, thus preserving the micellar structure in the dilution process. Information about the single micellar structure in the semidilute and concentrated region are extracted from structure factor analysis at high concentrations where the micelles order into fcc and bcc close packed lattices and the aggregation number can be calculated by geometrical arguments. This approach enables us to investigate the aggregation behavior in a wide concentration regime from dilute to 6·ϕ*, showing a constant aggregation number with concentration over a large concentration regime up to a critical concentration about three times ϕ*. When exceeding this critical concentration, the aggregation number was found to increase with increasing concentration. This behavior is compared to scaling theories for star-like polymer micelles.

  5. Computational fluid dynamics (CFD) simulations of dilute fluid-particle flows in aerosol concentrators

    NASA Astrophysics Data System (ADS)

    Hari, Sridhar

    2003-07-01

    In this study, commercially available Computational Fluid Dynamics (CFD) software, CFX-4.4 has been used for the simulations of aerosol transport through various aerosol-sampling devices. Aerosol transport was modeled as a classical dilute and dispersed two-phase flow problem. Eulerian-Lagrangian framework was adopted wherein the fluid was treated as the continuous phase and aerosol as the dispersed phase, with a one-way coupling between the phases. Initially, performance of the particle transport algorithm implemented in the code was validated against available experimental and numerical data in the literature. Code predictions were found to be in good agreement against experimental data and previous numerical predictions. As a next step, the code was used as a tool to optimize the performance of a virtual impactor prototype. Suggestions on critical geometrical details available in the literature, for a virtual impactor, were numerically investigated on the prototype and the optimum set of parameters was determined. Performance curves were generated for the optimized design at various operating conditions. A computational model of the Linear Slot Virtual Impactor (LSVI) fabricated based on the optimization study, was constructed using the worst-case values of the measured geometrical parameters, with offsets in the horizontal and vertical planes. Simulations were performed on this model for the LSVI operating conditions. Behavior of various sized particles inside the impactor was illustrated with the corresponding particle tracks. Fair agreement was obtained between code predictions and experimental results. Important information on the virtual impactor performance, not known earlier, or, not reported in the literature in the past, obtained from this study, is presented. In the final part of this study, simulations on aerosol deposition in turbulent pipe flow were performed. Code predictions were found to be completely uncorrelated to experimental data. The

  6. Time-resolved mass concentration, composition and sources of aerosol particles in a metropolitan underground railway station

    NASA Astrophysics Data System (ADS)

    Salma, Imre; Weidinger, Tamás; Maenhaut, Willy

    Aerosol samples were collected using a stacked filter unit (SFU) for PM10-2.0 and PM2.0 size fractions on the platform of a metropolitan underground railway station in downtown Budapest. Temporal variations in the PM10 mass concentration and wind speed and direction were determined with time resolutions of 30 and 4 s using a tapered-element oscillating microbalance (TEOM) and a wind monitor, respectively. Sample analysis involved gravimetry for particulate mass, and particle-induced X-ray emission spectrometry (PIXE) for elemental composition. Diurnal variation of the PM10 mass concentration exhibited two peaks, one at approximately 07:00 h and the other at approximately 17:00 h. The mean±SD PM10 mass concentration for working hours was 155±55 μg m -3. Iron, Mn, Ni, Cu, and Cr concentrations were higher than in outdoor air by factors between 5 and 20, showing substantial enrichment compared to both the average crustal rock composition and the average outdoor aerosol composition. Iron accounted for 40% and 46% of the PM10-2.0 and PM2.0 masses, respectively, and 72% of the PM10 mass was associated with the PM10-2.0 size fraction. The aerosol composition in the metro station (in particular the abundance of the metals mentioned above) is quite different from the average outdoor downtown composition. Mechanical wear and friction of electric conducting rails and bow sliding collectors, ordinary rails and wheels, as well as resuspension, were identified as the primary sources. Possible health implications based on comparison to various limit values and to data available for other underground railways are discussed.

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

    NASA Astrophysics Data System (ADS)

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

    2016-09-01

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

  8. The Impact of Monthly Variation of the Pacific-North America (PNA) Teleconnection Pattern on Wintertime Surface-layer Aerosol Concentrations in the United States

    NASA Astrophysics Data System (ADS)

    Feng, J.; Liao, H.; Li, J.

    2015-12-01

    The Pacific-North America teleconnection (PNA) is the leading general circulation pattern in the troposphere over the region of North Pacific to North America during wintertime. The PNA exhibits positive (negative) phases with positive (negative) anomalies in geopotential height in the vicinity of Hawaii and over the intermountain region of North America, and negative (positive) anomalies in geopotential height over south of the Aleutian Islands and the Gulf Coast region of the United States. This study examined the impacts of monthly variation of the PNA phase on wintertime surface-layer aerosol concentrations in the United States by analyzing observations during 1999-2013 from the Air Quality System of Environmental Protection Agency (EPA-AQS) and the model results for 1986-2006 from the global three-dimensional Goddard Earth Observing System (GEOS) chemical transport model (GEOS-Chem). The composite analyses on the EPA-AQS observations over 1999-2003 showed that the average PM2.5 concentrations were higher in the PNA positive phases than in the PNA negative phases by 1.0 μg m-3 (8.6%), 2.1μg m-3 (24.1%), and 1.1 μg m-3 (10.6%) in the eastern, western, and whole of United States, respectively. Relative to the PNA negative phases, the number of exceedance days (days with the PM2.5 concentrations exceeding 35 μg m-3) in the PNA positive phases increased by 5-8 days month-1 in California and the contiguous Great Salt Lake and by 2-3 days month-1 in Iowa. The simulated geographical patterns of the differences in concentrations of PM2.5, nitrate, sulfate, ammonium, OC, and BC between the PNA positive and negative phases were similar to observations. The PNA influences surface-layer aerosol concentrations in the United States by changing meteorological variables such as temperature, precipitation, planetary boundary layer height, relative humidity, and wind speed. We found that that the PNA-induced variation in planetary boundary layer height was the most dominant

  9. Seasonal evolution of anionic, cationic and non-ionic surfactant concentrations in coastal aerosols from Askö, Sweden

    NASA Astrophysics Data System (ADS)

    Gérard, Violaine; Nozière, Barbara; Baduel, Christine

    2015-04-01

    Surfactants present in atmospheric aerosols are expected to enhance the activation into cloud droplets by acting on one of the two key parameters of the Köhler equation: the surface tension, σ. But because the magnitude of this effect and its regional and temporal variability are still highly uncertain [1,2], various approaches have been developed to evidence it directly in the atmosphere. This work presents the analysis of surfactants present in PM2.5 aerosol fractions collected at the coastal site of Askö, Sweden (58° 49.5' N, 17° 39' E) from July to October 2010. The total surfactant fraction was extracted from the samples using an improved double extraction technique. Surface tension measurements performed with the pendant drop technique [3] indicated the presence of very strong surfactants (σ ~ 30 - 35 mN/m) in these aerosols. In addition, these extractions were combined with colorimetric methods to determine the anionic, cationic and non-ionic surfactant concentrations [4,5], and provided for the first time interference-free surfactant concentrations in atmospheric aerosols. At this site, the total surfactant concentration in the PM2.5 samples varied between 7 to 150 mM and was dominated by anionic and non-ionic ones. The absolute surface tension curves obtained for total surfactant fraction displayed Critical Micelle Concentrations (CMC) in the range 50 - 400 uM, strongly suggesting a biological origin for the surfactants. The seasonal evolution of these concentrations and their relationships with environmental or meteorological parameters at the site will be discussed. [1] Ekström, S., Nozière, B. et al., Biogeosciences, 2010, 7, 387 [2] Baduel, C., Nozière, B., Jaffrezo, J.-L., Atmos. Environ., 2012, 47, 413 [3] Nozière, B., Baduel, C., Jaffrezo, J.-L., Nat. Commun., 2014, 5, 1 [4] Latif, M. T.; Brimblecombe, P. Environ. Sci. Technol., 2004, 38, 6501 [5] Pacheco e Silva et al., Method to measure surfactant in fluid, 2013, US 2013/0337568 A1

  10. Regional background aerosols over the Balearic Islands over the last 3 years: ground-based concentrations, atmospheric deposition and sources

    NASA Astrophysics Data System (ADS)

    Cerro, Jose Carlos; Pey, Jorge; Bujosa, Carles; Caballero, Sandra; Alastuey, Andres; Sicard, Michael; Artiñano, Begoña; Querol, Xavier

    2013-04-01

    In the context of the ChArMEx (The Chemistry-Aerosol Mediterranean Experiment, https://charmex.lsce.ipsl.fr) initiative, a 3-year study over a regional background environment (Can Llompart, CLP) in Mallorca has been conducted. Ground-based PM mass concentrations, gaseous pollutants and meteorological parameters were continuously registered from 2010 to 2012. Since the beginning of the campaign, PM10 daily samples for chemical determinations were obtained every 4 days, and dry and wet deposition samples were collected every week. Moreover, additional instruments (condensation particle counter, multi-angle absorption photometer, airpointer, sequential high and low volume samplers) were deployed during intensive filed campaigns in 2011 and 2012, as well as the sampling frequency was intensified. In the laboratory, PM samples were analyzed for inorganic compounds, and organic and elemental carbon following different approaches. In addition, n-alkanes, iso-alkanes, antiso-alkanes, levoglucosan, alkanoic acids and cholesterol were determined by GC-MS chromatography in a selection of 30 samples. Mean PM10, PM2.5 and PM1 concentrations in the period 2010-2012 reached 17, 11, and 8 µg/m3 respectively. Mass concentrations displayed marked seasonal trends, with much higher background levels in summer due to stagnant conditions over the western Mediterranean and increased frequency of Saharan dust events. Likewise, diverse-intensity peaks of coarse PM due to African dust inputs were observed along the year. On average, African dust in PM10 accounted for 1.0-1.5 µg/m3. Sporadic pollution events, characterized by most of the particles in the fine mode, were related to the transport of anthropogenic polluted air masses from central and eastern Europe. Wet and dry atmospheric deposition samples are being analyzed to quantify the deposition fluxes for different soluble and insoluble compounds. On average, PM10 composition is made up of organic matter (23%), mineral components (17

  11. 40 CFR Table F-4 to Subpart F of... - Estimated Mass Concentration Measurement of PM2.5 for Idealized Coarse Aerosol Size Distribution

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 6 2012-07-01 2012-07-01 false Estimated Mass Concentration... Concentration Measurement of PM2.5 for Idealized Coarse Aerosol Size Distribution Particle Aerodynamic Diameter (µm) Test Sampler Fractional Sampling Effectiveness Interval Mass Concentration (µg/m3) Estimated...

  12. 40 CFR Table F-4 to Subpart F of... - Estimated Mass Concentration Measurement of PM 2.5 for Idealized Coarse Aerosol Size Distribution

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 6 2013-07-01 2013-07-01 false Estimated Mass Concentration... Concentration Measurement of PM 2.5 for Idealized Coarse Aerosol Size Distribution Particle Aerodynamic Diameter (µm) Test Sampler Fractional Sampling Effectiveness Interval Mass Concentration (µg/m 3)...

  13. 40 CFR Table F-6 to Subpart F of... - Estimated Mass Concentration Measurement of PM2.5 for Idealized Fine Aerosol Size Distribution

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 6 2012-07-01 2012-07-01 false Estimated Mass Concentration... Concentration Measurement of PM2.5 for Idealized Fine Aerosol Size Distribution Particle Aerodynamic Diameter (µm) Test Sampler Fractional Sampling Effectiveness Interval Mass Concentration (µg/m3) Estimated...

  14. 40 CFR Table F-4 to Subpart F of... - Estimated Mass Concentration Measurement of PM 2.5 for Idealized Coarse Aerosol Size Distribution

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 6 2014-07-01 2014-07-01 false Estimated Mass Concentration... Concentration Measurement of PM 2.5 for Idealized Coarse Aerosol Size Distribution Particle Aerodynamic Diameter (µm) Test Sampler Fractional Sampling Effectiveness Interval Mass Concentration (µg/m3) Estimated...

  15. 40 CFR Table F-6 to Subpart F of... - Estimated Mass Concentration Measurement of PM 2.5 for Idealized Fine Aerosol Size Distribution

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 6 2013-07-01 2013-07-01 false Estimated Mass Concentration... Concentration Measurement of PM 2.5 for Idealized Fine Aerosol Size Distribution Particle Aerodynamic Diameter (µm) Test Sampler Fractional Sampling Effectiveness Interval Mass Concentration (µg/m 3)...

  16. 40 CFR Table F-6 to Subpart F of... - Estimated Mass Concentration Measurement of PM 2.5 for Idealized Fine Aerosol Size Distribution

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 6 2014-07-01 2014-07-01 false Estimated Mass Concentration... Concentration Measurement of PM 2.5 for Idealized Fine Aerosol Size Distribution Particle Aerodynamic Diameter (µm) Test Sampler Fractional Sampling Effectiveness Interval Mass Concentration (µg/m3) Estimated...

  17. Regional Comparisons of Satellite (AVHRR) and Space Shuttle (MAPS) Derived Estimates of CO and Aerosol Concentrations

    NASA Technical Reports Server (NTRS)

    Vulcan, D. V.; Christopher, S. A.; Welch, R. M.; Connors, V. S.

    1996-01-01

    Biomass burning is considered to be a major source of trace gas species and aerosol particles which play a vital role in tropospheric chemistry and climate. Anthropogenic biomass burning has largely expanded in the last 15 years, due to increased deforestation practices in the Amazon Basin, as well as to clear land for shifting cultivation in South America, southern Asia, and Africa. Biomass burning produces large amounts of carbon dioxide, carbon monoxide (CO), water, hydrocarbons, nitrous oxides, and smoke particles.

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

    NASA Astrophysics Data System (ADS)

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

    2006-05-01

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

  19. 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

  20. Causes of seasonal and daily variations in aerosol sea-salt concentrations at a coastal Antarctic station

    NASA Astrophysics Data System (ADS)

    Hall, J. S.; Wolff, E. W.

    Two years worth of daily aerosol data has been collected from Halley station, Antarctica, between February 1991 and February 1993. The seasonal cycle of sea-salt aerosol was found to peak during the winter months, with an annual mean of 162 ng m -3. Specific site characteristics are used to explain this relatively low value. The winter sea-salt source does not appear to be solely due to the presence of open water. Comparison of individual high salt concentration events in the data, with 3 hourly meteorological records, shows that sea-salt loadings are not linked to high wind speeds, but more moderate ones. The high sea-salt loadings are associated with a change in wind direction that opens up an area of water and then switches to bring sea-salt inland. It is hypothesised that the exposed areas of sea water, which are rapidly frozen in winter creating areas of local, freshly formed ice with a surface covering of concentrated brine, are the source of the winter sea-salt. Fractionation of the sea-salt component in individual high concentration events, is used to reinforce the theory that a surface skim of highly saline brine, on fresh ice, is the winter sea-salt source. The presence of frost flowers is thought to aid incorporation of sea-salt into the atmosphere. Implications for the interpretation of sea-salt data in ice cores are highlighted.

  1. Mapping of PM10 surface concentrations derived from satellite observations of aerosol optical thickness over South-Eastern France

    NASA Astrophysics Data System (ADS)

    Péré, J.-C.; Pont, V.; Mallet, M.; Bessagnet, B.

    2009-01-01

    This work aims at developing a methodology based on in-situ experimental observations in order to use satellite retrievals as a tool for monitoring air particulate pollution. This methodology is applied during summer time on the South-Eastern France, which is one of the most polluted zones over Europe, enclosing further large cities and industrial sites. In a first time, we consider correlations between daily mean AERONET AOT and PM10 concentrations at five sites located as well close to as far from pollution sources. Our results show significant correlation coefficients, ranging from 0.68 to 0.79, following the site studied. Several factors like aerosol vertical distribution or hygroscopic growth factor could affect the link between PM10 ground measurements and aerosol optical thickness. To statistically strengthen this approach, we gather data sets from three types of sites (urban, near urban and rural) and establish a linear relationship between daily mean AOT measured from AERONET and PM10 mass concentrations. Secondly and thanks to good agreements between AOT measured from AERONET and AOT retrieved from the MODIS sensor, we calculate estimated concentrations of PM10 by using MODIS retrievals above the South-Eastern France. Uncertainties about this approach are discussed.

  2. Global Estimates of Ambient Fine Particulate Matter Concentrations from Satellite-Based Aerosol Optical Depth: Development and Application

    PubMed Central

    van Donkelaar, Aaron; Martin, Randall V.; Brauer, Michael; Kahn, Ralph; Levy, Robert; Verduzco, Carolyn; Villeneuve, Paul J.

    2010-01-01

    Background Epidemiologic and health impact studies of fine particulate matter with diameter < 2.5 μm (PM2.5) are limited by the lack of monitoring data, especially in developing countries. Satellite observations offer valuable global information about PM2.5 concentrations. Objective In this study, we developed a technique for estimating surface PM2.5 concentrations from satellite observations. Methods We mapped global ground-level PM2.5 concentrations using total column aerosol optical depth (AOD) from the MODIS (Moderate Resolution Imaging Spectroradiometer) and MISR (Multiangle Imaging Spectroradiometer) satellite instruments and coincident aerosol vertical profiles from the GEOS-Chem global chemical transport model. Results We determined that global estimates of long-term average (1 January 2001 to 31 December 2006) PM2.5 concentrations at approximately 10 km × 10 km resolution indicate a global population-weighted geometric mean PM2.5 concentration of 20 μg/m3. The World Health Organization Air Quality PM2.5 Interim Target-1 (35 μg/m3 annual average) is exceeded over central and eastern Asia for 38% and for 50% of the population, respectively. Annual mean PM2.5 concentrations exceed 80 μg/m3 over eastern China. Our evaluation of the satellite-derived estimate with ground-based in situ measurements indicates significant spatial agreement with North American measurements (r = 0.77; slope = 1.07; n = 1057) and with noncoincident measurements elsewhere (r = 0.83; slope = 0.86; n = 244). The 1 SD of uncertainty in the satellite-derived PM2.5 is 25%, which is inferred from the AOD retrieval and from aerosol vertical profile errors and sampling. The global population-weighted mean uncertainty is 6.7 μg/m3. Conclusions Satellite-derived total-column AOD, when combined with a chemical transport model, provides estimates of global long-term average PM2.5 concentrations. PMID:20519161

  3. Evaluation of the discmini personal aerosol monitor for submicrometer sodium chloride and metal aerosols

    NASA Astrophysics Data System (ADS)

    Mills, Jessica Breyan

    This work evaluated the robust, lightweight DiSCmini (DM) aerosol monitor for its ability to measure the concentration and mean diameter of submicrometer aerosols. Tests were conducted with monodispersed and polydispersed aerosols composed of two particle types (sodium chloride, NaCl, and spark generated metal particles, which simulate particles found in welding fume) at three different steady-state concentration ranges (Low, <103; Medium, 103-104; and High, >104 particles/cm3). Particle number concentration, lung deposited surface area (LDSA) concentration, and mean size measured with the DM were compared to those measured with reference instruments, a scanning mobility particle sizer (SMPS) and a handheld condensation particle counter (CPC). Particle number concentrations measured with the DM were within 16% of those measured by the CPC for polydispersed aerosols. Poorer agreement was observed for monodispersed aerosols (+/-35% for most tests and +101% for 300-nm NaCl). LDSA concentrations measured by the DM were 96% to 155% of those estimated with the SMPS. The geometric mean diameters measured with the DM were within 30% of those measured with the SMPS for monodispersed aerosols and within 25% for polydispersed aerosols (except for the case when the aerosol contained a substantial number of particles larger than 300 nm). The accuracy of the DM is reasonable for particles smaller than 300 nm but caution should be exercised when particles larger than 300 nm are present.

  4. Relation between cloud thickness-cloud number concentration differences and rain occurrence based on Koren-Feingold model

    NASA Astrophysics Data System (ADS)

    Sulistyowati, R.; Viridi, S.; Kurniadi, R.; Srigutomo, W.

    2016-11-01

    Koren-Feingold (KF) model, a model that relates growth of cloud thickness (H) and cloud number concentration (N) is discussed and analyzed in this work. Two boundary conditions are required by this model, where the first is cloud thickness potential H0 and the second is aerosol concentration N0 . The initial conditions are simply H(0) = 0 and N(0) = 0. Several pairs of (H0, N0) values are chosen in calculating the precipitation. Three categories of rainfall are used in this work, which are no drizzle D0, light drizzle D1, and drizzle D2. As H evolves in time t, it produces maximum cloud thickness Hmax and saturation cloud thickness Hsat , as also N does Nmax and Nsat . Two kinds of cloud thickness difference, ΔH1 = H0 - Hma x and ΔH2 = H0 - H sat are proposed and also for cloud concentration difference ΔN1 and ΔN2 with similar definitions. Pairs of (ΔH1 , ΔN1 ) and (ΔH2 , ΔN2 ) are used in analyzing simulation results. The first pair can be used as prediction of rainfall occurrence, while the second pair is more for confirmation and understanding the relation between cloud thickness and cloud concentration in producing rainfall. It is observed that H < H0 and N < N0 are always fulfilled. Rainfall in category D2 will have significant differences in H and N, while in category D0 will not. Typical differences for H are about 80% and 30-50% for both cases. Deeper discussion about (ΔH1 , ΔN1 ) and (ΔH2 , ΔN2 ) is presented in this work.

  5. Multicellular natural convection of a low Prandlt number fluid between horizontal concentric cylinders

    SciTech Connect

    Joosik Yoo; Jun Young Choi; Moonuhn Kim . Dept. of Mechanical Engineering)

    1994-01-01

    Two-dimensional natural convection of a fluid of low Prandtl number (Pr = 0.02) in an annulus between two concentric horizontal cylinders is numerically investigated in a wide range of gap widths. For low Grashof numbers, a steady unicellular convection is obtained. Above a transition Grashof number that depends on the gap width, a steady bicellular flow occurs. With further increase of the Grashof number, steady or time-periodic multicellular convection occurs, and finally, complex unsteady convective flow appears. A plot is presented that predicts the type of flow patterns for various combination of gap widths and Grashof numbers.

  6. Vertical variations of particle number concentration and size distribution in a street canyon in Shanghai, China.

    PubMed

    Li, X L; Wang, J S; Tu, X D; Liu, W; Huang, Z

    2007-06-01

    Measurements of particle number size distribution in the range of 10-487 nm were made at four heights on one side of an asymmetric street canyon on Beijing East Road in Shanghai, China. The result showed that the number size distributions were bimodal or trimodal and lognormal in form. Within a certain height from 1.5 to 20 m, the particle size distributions significantly changed with increasing height. The particle number concentrations in the nucleation mode and in the Aitken mode significantly dropped, and the peaking diameter in the Aitken mode shifted to larger sizes. The variations of the particle number size distributions in the accumulation mode were less significant than those in the nucleation and Aitken modes. The particle number size distributions slightly changed with increasing height ranging from 20 to 38 m. The particle number concentrations in the street canyon showed a stronger association with the pre-existing particle concentrations and the intensity of the solar radiation when the traffic flow was stable. The particle number concentrations were observed higher in Test I than in Test II, probably because the small pre-existing particle concentrations and the intense solar radiation promoted the formation of new particles. The pollutant concentrations in the street canyon showed a stronger association with wind speed and direction. For example, the concentrations of total particle surface area, total particle volume, PM2.5 and CO were lower in Test I (high wind speed and step-up canyon) than in Test II (low wind speed and wind blowing parallel to the canyon). The equations for the normalized concentration curves of the total particle number, CO and PM2.5 in Test I and Test II were derived. A power functions was found to be a good estimator for predicting the concentrations of total particle number, CO and PM2.5 at different heights. The decay rates of PM2.5 and CO concentrations were lower in Test I than in Test II. However, the decay rate of the

  7. MODELING AND EXPERIMENTAL EVALUATION OF AN AEROSOL GENERATOR FOR VERY HIGH NUMBER CURRENTS BASED ON A FREE TURBULENT JET. (R827354C008)

    EPA Science Inventory

    In this paper we report on theoretical and experimental work on aerosol formation in a free turbulent jet. A hot DEHS vapor issues through a circular nozzle into slowly moving cold air. Vapor concentration and temperatures are such that particles are formed via homogeneous nuc...

  8. Approximate Bayesian computation for estimating number concentrations of monodisperse nanoparticles in suspension by optical microscopy

    NASA Astrophysics Data System (ADS)

    Röding, Magnus; Zagato, Elisa; Remaut, Katrien; Braeckmans, Kevin

    2016-06-01

    We present an approximate Bayesian computation scheme for estimating number concentrations of monodisperse diffusing nanoparticles in suspension by optical particle tracking microscopy. The method is based on the probability distribution of the time spent by a particle inside a detection region. We validate the method on suspensions of well-controlled reference particles. We illustrate its usefulness with an application in gene therapy, applying the method to estimate number concentrations of plasmid DNA molecules and the average number of DNA molecules complexed with liposomal drug delivery particles.

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

    SciTech Connect

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

    2013-01-24

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

  10. A Nanometer Aerosol Size Analyzer (nASA) for Rapid Measurement of High-concentration Size Distributions

    NASA Astrophysics Data System (ADS)

    Han, Hee-Siew; Chen, Da-Ren; Pui, David Y. H.; Anderson, Bruce E.

    2000-03-01

    We have developed a fast-response nanometer aerosol size analyzer (nASA) that is capable of scanning 30 size channels between 3 and 100 nm in a total time of 3 s. The analyzer includes a bipolar charger (Po210), an extended-length nanometer differential mobility analyzer (Nano-DMA), and an electrometer (TSI 3068). This combination of components provides particle size spectra at a scan rate of 0.1 s per channel free of uncertainties caused by response-time-induced smearing. The nASA thus offers a fast response for aerosol size distribution measurements in high-concentration conditions and also eliminates the need for applying a de-smearing algorithm to resulting data. In addition, because of its thermodynamically stable means of particle detection, the nASA is useful for applications requiring measurements over a broad range of sample pressures and temperatures. Indeed, experimental transfer functions determined for the extended-length Nano-DMA using the tandem differential mobility analyzer (TDMA) technique indicate the nASA provides good size resolution at pressures as low as 200 Torr. Also, as was demonstrated in tests to characterize the soot emissions from the J85-GE engine of a T-38 aircraft, the broad dynamic concentration range of the nASA makes it particularly suitable for studies of combustion or particle formation processes. Further details of the nASA performance as well as results from calibrations, laboratory tests and field applications are presented below.

  11. A Nanometer Aerosol Size Analyzer (nASA) for Rapid Measurement of High-Concentration Size Distributions

    NASA Technical Reports Server (NTRS)

    Han, Hee-Siew; Chen, Da-Ren; Pui, David Y. H.; Anderson, Bruce E.

    2001-01-01

    We have developed a fast-response Nanometer Aerosol Size Analyzer (nASA) that is capable of scanning 30 size channels between 3 and 100 nm in a total time of 3 seconds. The analyzer includes a bipolar charger (P0210), an extended-length Nanometer Differential Mobility Analyzer (Nano-DMA), and an electrometer (TSI 3068). This combination of components provides particle size spectra at a scan rate of 0.1 second per channel free of uncertainties caused by response-time-induced smearing. The nASA thus offers a fast response for aerosol size distribution measurements in high-concentration conditions and also eliminates the need for applying a de-smearing algorithm to resulting data. In addition, because of its thermodynamically stable means of particle detection, the nASA is useful for applications requiring measurements over a broad range of sample pressures and temperatures. Indeed, experimental transfer functions determined for the extended-length Nano-DMA using the Tandem Differential Mobility Analyzer (TDMA) technique indicate the nASA provides good size resolution at pressures as low as 200 Torr. Also, as was demonstrated in tests to characterize the soot emissions from the J85-GE engine of a T38 aircraft, the broad dynamic concentration range of the nASA makes it particularly suitable for studies of combustion or particle formation processes. Further details of the nASA performance as well as results from calibrations, laboratory tests and field applications are presented.

  12. Quantitative measurement of the nanoparticle size and number concentration from liquid suspensions by atomic force microscopy.

    PubMed

    Baalousha, M; Prasad, A; Lead, J R

    2014-05-01

    Microscopy techniques are indispensable to the nanoanalytical toolbox and can provide accurate information on the number size distribution and number concentration of nanoparticles (NPs) at low concentrations (ca. ppt to ppb range) and small sizes (ca. <20 nm). However, the high capabilities of microscopy techniques are limited by the traditional sample preparation based on drying a small volume of suspension of NPs on a microscopy substrate. This method is limited by low recovery of NPs (ca. <10%), formation of aggregates during the drying process, and thus, the complete misrepresentation of the NP suspensions under consideration. This paper presents a validated quantitative sampling technique for atomic force microscopy (AFM) that overcomes the above-mentioned shortcomings and allows full recovery and representativeness of the NPs under consideration by forcing the NPs into the substrate via ultracentrifugation and strongly attaches the NPs to the substrate by surface functionalization of the substrate or by adding cations to the NP suspension. The high efficiency of the analysis is demonstrated by the uniformity of the NP distribution on the substrate (that is low variability between the number of NPs counted on different images on different areas of the substrate), the high recovery of the NPs up to 71%) and the good correlation (R > 0.95) between the mass and number concentrations. Therefore, for the first time, we developed a validated quantitative sampling technique that enables the use of the full capabilities of microscopy tools to quantitatively and accurately determine the number size distribution and number concentration of NPs at environmentally relevant low concentrations (i.e. 0.34-100 ppb). This approach is of high environmental relevance and can be applied widely in environmental nanoscience and nanotoxicology for (i) measuring the number concentration dose in nanotoxicological studies and (ii) accurately measuring the number size distribution of

  13. Evaluation of the diffusion size classifier (meDiSC) for the real-time measurement of particle size and number concentration of nanoaerosols in the range 20-700 nm.

    PubMed

    Bau, Sébastien; Jacoby, Jonathan; Witschger, Olivier

    2012-03-01

    In the frame of assessing exposure to nanostructured particles, the aim of this work is to study the performance of a new device devoted to the real-time measurement of nanostructured aerosol: the meDiSC (Diffusion Size Classifier, Matter Engineering, Switzerland). This instrument is based on unipolar diffusion charging of particles which are then collected successively in diffusion and filtration stages. From currents measured in these stages, the instrument is capable of determining aerosol mean size and number concentration. These data were compared to reference measurements regarding monodisperse aerosols in a range from 20 to 700 nm; the relative biases were found unsatisfying. This led us to investigate the principle of the instrument. Consequently, the charging law of the diffusion charger was experimentally established, as well as the calibration curve allowing the determination of the mean size of the particles. The latter analysis was completed by a model based on diffusion theory. Our results indicate the possibility to improve the range of size measurement up to 350 nm. Measured particle size and number concentration were also used to calculate geometric surface-area concentration; the experimental data were compared to a reference calculated surface-area concentration. The results demonstrate the possibility to evaluate this parameter within acceptable uncertainty. In a second step, the meDiSC was challenged with polydisperse aerosols. It was observed that meDiSC overestimates particle size by a factor 1.7, while particle number concentrations are found within ±40% of the reference. The model applied to polydisperse aerosols indicates that polydispersity little influences particle size up to 300 nm while geometric standard deviation remains below 1.7.

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

    NASA Astrophysics Data System (ADS)

    Li, G.; Zavala, M.; Lei, W.; Tsimpidi, A. P.; Karydis, V. A.; Pandis, S. N.; Canagaratna, M. R.; Molina, L. T.

    2011-04-01

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

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

    NASA Astrophysics Data System (ADS)

    Li, G.; Zavala, M.; Lei, W.; Tsimpidi, A. P.; Karydis, V. A.; Pandis, S. N.; Molina, L. T.

    2010-12-01

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

  16. Effect of oxidant concentration, exposure time, and seed particles on secondary organic aerosol chemical composition and yield

    DOE PAGES

    Lambe, A. T.; Chhabra, P. S.; Onasch, T. B.; ...

    2015-03-18

    We performed a systematic intercomparison study of the chemistry and yields of secondary organic aerosol (SOA) generated from OH oxidation of a common set of gas-phase precursors in a Potential Aerosol Mass (PAM) continuous flow reactor and several environmental chambers. In the flow reactor, SOA precursors were oxidized using OH concentrations ranging from 2.0 × 108 to 2.2 × 1010 molec cm-3 over exposure times of 100 s. In the environmental chambers, precursors were oxidized using OH concentrations ranging from 2 × 106 to 2 × 107 molec cm-3 over exposure times of several hours. The OH concentration in themore » chamber experiments is close to that found in the atmosphere, but the integrated OH exposure in the flow reactor can simulate atmospheric exposure times of multiple days compared to chamber exposure times of only a day or so. In most cases, for a specific SOA type the most-oxidized chamber SOA and the least-oxidized flow reactor SOA have similar mass spectra, oxygen-to-carbon and hydrogen-to-carbon ratios, and carbon oxidation states at integrated OH exposures between approximately 1 × 1011 and 2 × 1011 molec cm-3 s, or about 1–2 days of equivalent atmospheric oxidation. This observation suggests that in the range of available OH exposure overlap for the flow reactor and chambers, SOA elemental composition as measured by an aerosol mass spectrometer is similar whether the precursor is exposed to low OH concentrations over long exposure times or high OH concentrations over short exposure times. This similarity in turn suggests that both in the flow reactor and in chambers, SOA chemical composition at low OH exposure is governed primarily by gas-phase OH oxidation of the precursors rather than heterogeneous oxidation of the condensed particles. In general, SOA yields measured in the flow reactor are lower than measured in chambers for the range of equivalent OH exposures that can be measured in both the flow reactor and chambers. The influence of

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

    NASA Astrophysics Data System (ADS)

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

    2006-12-01

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

  18. ANALYSIS OF RESPIRATORY DEPOSITION OF INHALED PARTICLES FOR DIFFERENT DOSE METRICS: COMPARISON OF NUMBER, SURFACE AREA AND MASS DOSE OF TYPICAL AMBIENT BI-MODAL AEROSOLS

    EPA Science Inventory

    ANALYSIS OF RESPIRATORY DEPOSITION OF INHALED PARTICLES FOR DIFFERENT DOSE METRICS: COMPARISON OF NUMBER, SURFACE AREA AND MASS DOSE OF TYPICAL AMBIENT BI-MODAL AEROSOLS.
    Chong S. Kim, SC. Hu*, PA Jaques*, US EPA, National Health and Environmental Effects Research Laboratory, ...

  19. Effect of spermatozoal concentration and number on fertility of frozen equine semen.

    PubMed

    Leipold, S D; Graham, J K; Squires, E L; McCue, P M; Brinsko, S P; Vanderwall, D K

    1998-06-01

    Information on the number of motile spermatozoa needed to maximize pregnancy rates for frozen-thawed stallion semen is limited. Furthermore, concentration of spermatozoa per 0.5-mL straw has been shown to affect post-thaw motility (7). The objectives of this study were 1) to compare the effect of increasing the concentration of spermatozoa in 0.5-mL straws from 400 to 1,600 x 10(6) spermatozoa/mL on pregnancy rate of mares, and 2) to determine whether increasing the insemination dose from approximately 320 to 800 million progressively motile spermatozoa after thawing would increase pregnancy rates. Several ejaculates from each of 5 stallions were frozen in a skim milk-egg yolk based freezing medium at 2 spermatozoal concentrations in 0.5-mL polyvinyl-chloride straws. Half of each ejaculate was frozen at 400 x 10(6) cells/mL and half at 1,600 x 10(6) cells/mL. Insemination doses were based on post-thaw spermatozoal motility and contained approximately 320 x 10(6) (320 to 400) motile spermatozoa or approximately 800 x 10(6) (800 to 900) motile spermatozoa. Sixty-three mares were assigned to 1 of 4 spermatozoal treatments (1--low spermatozoal number, low concentration; 2--low spermatozoal number, high concentration; 3--high spermatozoal number, low concentration; 4--high spermatozoal number, high concentration) and were inseminated daily. Post-thaw spermatozoal motility was similar for cells frozen at both spermatozoal concentrations (P > 0.1). One-cycle pregnancy rates were 15, 40, 28 and 33%, respectively, for Treatments 1, 2, 3 and 4. Packaging spermatozoa at the high concentration tended to increase pregnancy rates vs packaging at the low concentration (37 vs 22%; P = 0.095). Furthermore, when the lower spermatozoal number was used, there tended (P < 0.1) to be a higher pregnancy rate if spermatozoa were packaged at the higher concentration. There was no increase in pregnancy rates when higher numbers of motile spermatozoa were inseminated (27 vs 31%; P > 0

  20. [Use of laser flow-type fluorescence aerosol particle counter to evaluate the concentration of microbes in the surface air under high dust content].

    PubMed

    Kalinin, Iu T; Vorob'ev, S A; Khramov, E N; Vorob'eva, E A; Kuznetsov, A P; Kiselev, O S

    2000-01-01

    The paper deals with the use of a laser flow-type fluorescence aerosol particle counter to evaluate the concentrations of microbes in the surface air under high dust content. Various circuits of flow-type optic aerosol recorders are analyzed. Flow spectral luminescence analysis of some particles flow while exciting the fourth harmonics of a pulse laser on yttrium-aluminium garnet with neodymium by ultraviolet radiation is shown to be the most optimum method for indication of individual aerosol particles. Experiments were conducted on the authors' model of a pilot plant based on this method. The model of a laser flow-type optic analyzer was developed for experimental studies that give a clear display of biological aerosols in complex aerosols. The laser flow-type analyzer-based unit developed may provide a fluorescence signal of aerosol particles in the flow of a sample and that light diffusion signal from them at an exciting light wavelength of 266 nm. Experiments with BVC aerosols and soil dust particles were conducted in different regions of Russia. They showed it possible to detect and to rapidly calculate soil microorganisms by laser flow-type fluorescence assay of individual particles when excited by ultraviolet radiation.

  1. Predictions of size-resolved aerosol concentrations of ammonium, chloride and nitrate at a bayside site using EQUISOLV II

    NASA Astrophysics Data System (ADS)

    Campbell, Scott W.; Evans, Melissa C.; Poor, Noreen D.

    Measured ambient air concentrations of ammonium, chloride and nitrate were compared with concentrations produced by EQUISOLV II, an aerosol thermodynamic equilibrium model. The monitoring equipment was located ˜50 m from Old Tampa Bay at the eastern end of the Gandy Bridge in Tampa, FL. Size-segregated ion concentrations of ammonium, sodium, potassium, calcium, magnesium, fluoride, chloride, nitrite, nitrate, sulfate and phosphate were determined from 6- and 1-day integrated cascade impactor samples obtained in May and August 2001, respectively. EQUISOLV II was initialized with these ion concentrations by size bin, and by gas phase concentrations of the volatile species, acquired with a collocated annular denuder system. The model redistributed the ions between the size bins until gas and particle concentrations reached equilibrium. The model calculated predominantly fine particle ammonium and coarse particle chloride and nitrate. For the May sampling period, when the average relative humidity was below 65%, the model predicted the formation of seven solids KNO 3, K 2SO 4, (NH 4) 2SO 4, Na 2SO 4, NaCl, NaNO 3, and CaSO 4·2H 2O. The amounts of ammonium in the fine fraction and of nitrate and chloride in the coarse fraction were predicted within the combined measurement and modeling uncertainty in the majority of cases.

  2. 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

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

    NASA Astrophysics Data System (ADS)

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

    2009-12-01

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

  4. Aerosol cloud processing with the global model ECHAM5-HAM-SALSA

    NASA Astrophysics Data System (ADS)

    Bergman, T.; Korhonen, H.; Zubair, M.; Romakkaniemi, S.; Lehtinen, K.; Kokkola, H.

    2012-04-01

    Atmospheric aerosols and their interactions with clouds constitute the largest uncertainty in the radiative forcing of the Earth's atmosphere. Increasing aerosol number concentrations increases the cloud droplet concentration and droplet surface and hence the cloud albedo. This mechanism is called the aerosol indirect effect on climate. Understanding the changes in cloud droplet number concentrations and size by anthropogenic aerosols are the key factors in the study of future climate change. Therefore the aerosols' formation and growth from nanoparticles to cloud condensation nuclei (CCN) must be described accurately. The formation and growth of aerosols are shown to be described more accurately with sectional representations than with bulk (total aerosol mass only), modal (lognormal modes describing mass and number size distribution) or moment (processes tied to different moments of particle number size distribution) approaches. Recently the sectional aerosol models have been implemented to global climate models. However, the resolution of sectional models must be optimised to reduce the computational cost. We have implemented the sectional aerosol model SALSA in ECHAM5-HAM. SALSA describes the aerosol population with 20 size sections. The dynamics are optimised for large scale applications and the model includes an improved moving center sectional method. The particulate mass consists of five compounds: sulphate, organic carbon, black carbon, sea salt and dust. The aerosol processing has been studied extensively and there are many numerical models used to predict CCN number concentrations. However, due to computational limitations many of them are not suitable for utilisation in global climate models. Therefore in most global climate studies on aerosol activation to CCN is examined using cloud activation parameterisations. We study the aerosol cloud processing and its affect on transport of aerosols using Abdul-Razzak-Ghan aerosol cloud activation

  5. A Simple Model of Global Aerosol Indirect Effects

    SciTech Connect

    Ghan, Steven J.; Smith, Steven J.; Wang, Minghuai; Zhang, Kai; Pringle, K. J.; Carslaw, K. S.; Pierce, Jeffrey; Bauer, Susanne E.; Adams, P. J.

    2013-06-28

    Most estimates of the global mean indirect effect of anthropogenic aerosol on the Earth’s energy balance are from simulations by global models of the aerosol lifecycle coupled with global models of clouds and the hydrologic cycle. Extremely simple models have been developed for integrated assessment models, but lack the flexibility to distinguish between primary and secondary sources of aerosol. Here a simple but more physically-based model expresses the aerosol indirect effect using analytic representations of droplet nucleation, cloud and aerosol vertical structure, and horizontal variability in cloud water and aerosol concentration. Although the simple model is able to produce estimates of aerosol indirect effects that are comparable to those from some global aerosol models using the same global mean aerosol properties, the estimates are found to be sensitive to several uncertain parameters, including the preindustrial cloud condensation nuclei concentration, primary and secondary anthropogenic emissions, the size of the primary particles, the fraction of the secondary anthropogenic emissions that accumulates on the coarse mode, the fraction of the secondary mass that forms new particles, and the sensitivity of liquid water path to droplet number concentration. Aerosol indirect effects are surprisingly linear in emissions. This simple model provides a much stronger physical basis for representing aerosol indirect effects than previous representations in integrated assessment models designed to quickly explore the parameter space of emissions-climate interactions. The model also produces estimates that depend on parameter values in ways that are consistent with results from detailed global aerosol-climate simulation models.

  6. [Study on number concentration distribution of atmospheric ultrafine particles in Hangzhou].

    PubMed

    Xie, Xiao-Fang; Sun, Zai; Fu, Zhi-Min; Yang, Wen-Jun; Lin, Jian-Zhong

    2013-02-01

    Atmospheric ultrafine particles (UFPs) were measured with fast mobility particle sizer(FMPS) in Hangzhou, during March 2011 to February 2012. The number concentration and size distribution of UFPs associated with meteorology were studied. The results showed that the number concentration of UFPs was logarithmic bi-modal distribution, and the seasonal levels presented winter > summer > spring> autumn. The highest monthly average concentration was 3.56 x 10(4) cm-3 in December and the lowest was 2.51 x 10(4) cm-3 in October. The seasonal values of count medium diameter(CMD) were spring > winter > autumn > summer. The highest monthly average CMD was 53. 51 nm in April and the lowest was 16.68 nm in June. Meteorological factors had effects on concentration of UFPs.

  7. Measurement of particle number and related pollutant concentrations in an urban area in South Brazil

    NASA Astrophysics Data System (ADS)

    Agudelo-Castañeda, D. M.; Teixeira, E. C.; Rolim, S. B. A.; Pereira, F. N.; Wiegand, F.

    2013-05-01

    The purpose of the present study was to analyze atmospheric particle number concentration at Sapucaia do Sul, in the Metropolitan Area of Porto Alegre, and associate it with the pollutants NO, NO2, and O3. Measurements were performed in two periods: August to October, in 2010 and 2011. We used the following equipment: the continuous particulate monitor (CPM), the chemiluminescent nitrogen oxide analyzer (AC32M), and the UV photometric ozone analyzer (O342M). Daily and hourly particle number concentrations in fractions PR1.0 (0.3-1.0 μm), PR2.5 (1.0-2.5 μm), and PR10 (2.5-10 μm), and concentrations of pollutants NO, NO2, NOx, and O3 were measured. These data were correlated with meteorological parameters such as wind speed, temperature, relative humidity, and solar radiation. The daily variation of OX (NO2 + O3) and its relation with NO2 were also established. The results obtained for daily particle number concentration (particles L-1) showed that the area of study had higher particle number of PR2.5 and PR1.0 size ranges, with values of 19.5 and 28.51 particles L-1, respectively. Differences in particle number concentrations in PR1 and PR2.5 size ranges were found between weekdays and weekends. The daily variation per hour of concentrations of particle number, NO, and NOx showed peaks during increased traffic flow in the morning and in the evening. NO2 showed peaks at different times, with the first peak (morning) 2 h after the peak of NO, and a second peak in the evening (19:00). This is due to the oxidation of NO and to the photolysis of NO3 formed overnight. Correlation analysis suggests that there may be a relationship between the fine and ultrafine particles and NO, probably indicating that they have similar sources, such as vehicular emissions. In addition, a possible relationship of solar radiation with fine particle number concentrations, as well as with O3 was also observed. The results, too, show an inverse relationship between particle number

  8. Assessing the use of VIIRS Aerosol Intermediate Product for AOD retrieval and PM25 concentrations.

    NASA Astrophysics Data System (ADS)

    Gross, B.; Nazmi, C.; Moshary, F.; Lightstone, S.

    2015-12-01

    In previous work, it was shown that MODIS AOD retreivals over urban areas have overbiases that can be removed if proper account is made of the surface land classification. In fact, both direct methods where improvements to urban model albedos were implemented as well as post processing approaches using Neural Networks (NN's) were shown to be useful in reducing biases and retreival uncertainty. In this paper, we make a preliminary study of these approaches to the VIIRS Intermediate Aerosol Optical Depth Product and demonstrate that VIIRS Biases can also be substantially reduced. Comparisons with MODIS will be made and direct use of the high resolution product will be used to assess potential PM25 estimation.

  9. Aerosol Variability Observed with Rpas

    NASA Astrophysics Data System (ADS)

    Altstädter, B.; Lampert, A.; Scholtz, A.; Bange, J.; Platis, A.; Hermann, M.; Wehner, B.

    2013-08-01

    To observe the origin, vertical and horizontal distribution and variability of aerosol particles, and especially ultrafine particles recently formed, we plan to employ the remotely piloted aircraft system (RPAS) Carolo-P360 "ALADINA" of TU Braunschweig. The goal of the presented project is to investigate the vertical and horizontal distribution, transport and small-scale variability of aerosol particles in the atmospheric boundary layer using RPAS. Two additional RPAS of type MASC of Tübingen University equipped with turbulence instrumentation add the opportunity to study the interaction of the aerosol concentration with turbulent transport and exchange processes of the surface and the atmosphere. The combination of different flight patterns of the three RPAS allows new insights in atmospheric boundary layer processes. Currently, the different aerosol sensors are miniaturized at the Leibniz Institute for Tropospheric Research, Leipzig and together with the TU Braunschweig adapted to fit into the RPAS. Moreover, an additional meteorological payload for measuring temperature, humidity and turbulence properties is constructed by Tübingen University. Two condensation particle counters determine the total aerosol number with a different lower detection threshold in order to investigate the horizontal and vertical aerosol variability and new particle formation (aerosol particles of some nm diameter). Further the aerosol size distribution in the range from about 0.300 to ~5 μm is given by an optical particle counter.

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

    NASA Astrophysics Data System (ADS)

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

    2014-05-01

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

  11. Impact of particle formation on atmospheric ions and particle number concentrations in an urban environment

    NASA Astrophysics Data System (ADS)

    Cheung, H. C.; Chou, C. C.-K.; Jayaratne, E. R.; Morawska, L.

    2015-04-01

    A measurement campaign was conducted from 3 to 19 December 2012 at an urban site of Brisbane, Australia. Size distribution of ions and particle number concentrations were measured to investigate the influence of particle formation and biomass burning on atmospheric ion and particle concentrations. Overall ion and particle number concentrations during the measurement period were found to be (- 1.2 × 103 cm- 3 | + 1.6 × 103 cm- 3) and 4.4 × 103, respectively. The results of correlation analysis between concentrations of ions and nitrogen oxides indicated that positive and negative ions originated from similar sources, and that vehicle exhaust emissions had a more significant influence on intermediate/large ions, while cluster ions rapidly attached to larger particles once emitted into the atmosphere. Diurnal variations in ion concentration suggested the enrichment of intermediate and large ions on new particle formation event days, indicating that they were involved in the particle formation processes. Elevated total ions, particularly larger ions, and particle number concentrations were found during biomass burning episodes. This could be due to the attachment of cluster ions onto accumulation mode particles or production of charged particles from biomass burning, which were in turn transported to the measurement site. The results of this work enhance scientific understanding of the sources of atmospheric ions in an urban environment, as well as their interactions with particles during particle formation processes.

  12. The self-preserving size distribution theory. I. Effects of the Knudsen number on aerosol agglomerate growth.

    PubMed

    Dekkers, Petrus J; Friedlander, Sheldon K

    2002-04-15

    Gas-phase synthesis of fine solid particles leads to fractal-like structures whose transport and light scattering properties differ from those of their spherical counterparts. Self-preserving size distribution theory provides a useful methodology for analyzing the asymptotic behavior of such systems. Apparent inconsistencies in previous treatments of the self-preserving size distributions in the free molecule regime are resolved. Integro-differential equations for fractal-like particles in the continuum and near continuum regimes are derived and used to calculate the self-preserving and quasi-self-preserving size distributions for agglomerates formed by Brownian coagulation. The results for the limiting case (the continuum regime) were compared with the results of other authors. For these cases the finite difference method was in good in agreement with previous calculations in the continuum regime. A new analysis of aerosol agglomeration for the entire Knudsen number range was developed and compared with a monodisperse model; Higher agglomeration rates were found for lower fractal dimensions, as expected from previous studies. Effects of fractal dimension, pressure, volume loading and temperature on agglomerate growth were investigated. The agglomeration rate can be reduced by decreasing volumetric loading or by increasing the pressure. In laminar flow, an increase in pressure can be used to control particle growth and polydispersity. For D(f)=2, an increase in pressure from 1 to 4 bar reduces the collision radius by about 30%. Varying the temperature has a much smaller effect on agglomerate coagulation.

  13. Seasonal variation of atmospheric particle number concentrations, new particle formation and atmospheric oxidation capacity at the high Arctic site Villum Research Station, Station Nord

    NASA Astrophysics Data System (ADS)

    Nguyen, Quynh T.; Glasius, Marianne; Sørensen, Lise L.; Jensen, Bjarne; Skov, Henrik; Birmili, Wolfram; Wiedensohler, Alfred; Kristensson, Adam; Nøjgaard, Jacob K.; Massling, Andreas

    2016-09-01

    This work presents an analysis of the physical properties of sub-micrometer aerosol particles measured at the high Arctic site Villum Research Station, Station Nord (VRS), northeast Greenland, between July 2010 and February 2013. The study focuses on particle number concentrations, particle number size distributions and the occurrence of new particle formation (NPF) events and their seasonality in the high Arctic, where observations and characterization of such aerosol particle properties and corresponding events are rare and understanding of related processes is lacking.A clear accumulation mode was observed during the darker months from October until mid-May, which became considerably more pronounced during the prominent Arctic haze months from March to mid-May. In contrast, nucleation- and Aitken-mode particles were predominantly observed during the summer months. Analysis of wind direction and wind speed indicated possible contributions of marine sources from the easterly side of the station to the observed summertime particle number concentrations, while southwesterly to westerly winds dominated during the darker months. NPF events lasting from hours to days were mostly observed from June until August, with fewer events observed during the months with less sunlight, i.e., March, April, September and October. The results tend to indicate that ozone (O3) might be weakly anti-correlated with particle number concentrations of the nucleation-mode range (10-30 nm) in almost half of the NPF events, while no positive correlation was observed. Calculations of air mass back trajectories using the Hybrid Single Particle Lagrangian Integrated Trajectory (HYSPLIT) model for the NPF event days suggested that the onset or interruption of events could possibly be explained by changes in air mass origin. A map of event occurrence probability was computed, indicating that southerly air masses from over the Greenland Sea were more likely linked to those events.

  14. How Important Is Organic Aerosol Hygroscopicity to Aerosol Indirect Forcing?

    SciTech Connect

    Liu, Xiaohong; Wang, Jian

    2010-12-07

    Organics are among the most abundant aerosol components in the atmosphere. However, there are still large uncertainties with emissions of primary organic aerosol (POA) and volatile organic compounds (VOCs) (precursor gases of secondary organic aerosol, SOA), formation and yield of SOA, and chemical and physical properties (e.g., hygroscopicity) of POA and SOA. All these may have significant impacts on aerosol direct and indirect forcing estimated from global models. In this study a modal aerosol module (MAM) in the NCAR Community Atmospheric Model (CAM) is used to examine sensitivities of aerosol indirect forcing to hygroscopicity (“κ” value) of POA and SOA. Our model simulation indicates that in the present-day condition changing “κ” value of POA from 0 to 0.1 increases the number concentration of cloud condensational nuclei (CCN) at supersaturation S=0.1% by 40-60% over the POA source regions, while changing “κ” value of SOA by ±50% (from 0.14 to 0.07 and 0.21) changes the CCN within 30%. Changes in the in-cloud droplet number concentrations (CDNC) are within 20% in most locations on the globe with the above changes in “κ” value of POA and SOA. Global annual mean anthropogenic aerosol indirect forcing (AIF) between present-day (PD) and pre-industrial (PI) conditions change by 0.4 W m-2 with the control run of -1.3 W m-2. AIF reduces with the increase hygroscopicity of organic aerosol, indicating the important role of natural organic aerosol in buffering the relative change of CDNC from PI to PD.

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

    NASA Astrophysics Data System (ADS)

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

    2010-05-01

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

  16. The Effects of Vegetation Barriers on Near-road Ultrafine Particle Number and Carbon Monoxide Concentrations

    EPA Science Inventory

    Numerous studies have shown that people living in near-roadway communities (within 100 m of the road) are exposed to high ultrafine particle (UFP) number concentrations, which may be associated with adverse health effects. Vegetation barriers have been shown to affect pollutant t...

  17. Vehicle and driving characteristics that influence in-cabin particle number concentrations.

    PubMed

    Hudda, Neelakshi; Kostenidou, Evangelia; Sioutas, Constantinos; Delfino, Ralph J; Fruin, Scott A

    2011-10-15

    In-transit microenvironments experience elevated levels of vehicle-related pollutants such as ultrafine particles. However, in-vehicle particle number concentrations are frequently lower than on-road concentrations due to particle losses inside vehicles. Particle concentration reduction occurs due to a complicated interplay between a vehicle's air-exchange rate (AER), which determines particle influx rate, and particle losses due to surfaces and the in-cabin air filter. Accurate determination of inside-to-outside particle concentration ratios is best made under realistic aerodynamic and AER conditions because these ratios and AER are determined by vehicle speed and ventilation preference, in addition to vehicle characteristics such as age. In this study, 6 vehicles were tested at 76 combinations of driving speeds, ventilation conditions (i.e., outside air or recirculation), and fan settings. Under recirculation conditions, particle number attenuation (number reduction for 10-1000 nm particles) averaged 0.83 ± 0.13 and was strongly negatively correlated with increasing AER, which in turn depended on speed and the age of the vehicle. Under outside air conditions, attenuation averaged 0.33 ± 0.10 and primarily decreased at higher fan settings that increased AER. In general, in-cabin particle number reductions did not vary strongly with particle size, and cabin filters exhibited low removal efficiencies.

  18. Global and regional evolution of short-lived radiatively-active gases and aerosols in the Representative Concentration Pathways

    SciTech Connect

    Lamarque, J.-F.; Kyle, G. Page; Meinshausen, Malte; Riahi, Keywan; Smith, Steven J.; Van Vuuren, Detlef; Conley, Andrew; Vitt, Francis

    2011-08-05

    In this paper, we discuss the results of 2000-2100 simulations with a chemistry-climate model, focusing on the changes in atmospheric composition (troposphere and stratosphere) following the emissions associated with the Representative Concentration Pathways. We show that tropospheric ozone is projected to decrease (RCP3PD and RCP4.5) or increase (RCP8.5) between 2000 and 2100. Surface ozone in 2100 is projected to change little compared from 2000 conditions, a much-reduced impact from the projections based on the A2 scenario. Aerosols are projected to strongly decrease in the 21st century, a reflection of their projected decrease in emissions. Similarly, sulfate deposition is projected to strongly decrease. However, nitrogen deposition is projected to increase over certain regions because of the projected increase NH3 emissions.

  19. The MODIS Aerosol Algorithm, Products and Validation

    NASA Technical Reports Server (NTRS)

    Remer, L. A.; Kaufman, Y. J.; Tanre, D.; Mattoo, S.; Chu, D. A.; Martins, J. V.; Li, R.-R.; Ichoku, C.; Levy, R. C.; Kleidman, R. G.

    2003-01-01

    The MODerate resolution Imaging Spectroradiometer (MODIS) aboard both NASA's Terra and Aqua satellites is making near global daily observations of the earth in a wide spectral range. These measurements are used to derive spectral aerosol optical thickness and aerosol size parameters over both land and ocean. The aerosol products available over land include aerosol optical thickness at three visible wavelengths, a measure of the fraction of aerosol optical thickness attributed to the fine mode and several derived parameters including reflected spectral solar flux at top of atmosphere. Over ocean, the aerosol optical thickness is provided in seven wavelengths from 0.47 microns to 2.13 microns. In addition, quantitative aerosol size information includes effective radius of the aerosol and quantitative fraction of optical thickness attributed to the fine mode. Spectral aerosol flux, mass concentration and number of cloud condensation nuclei round out the list of available aerosol products over the ocean. The spectral optical thickness and effective radius of the aerosol over the ocean are validated by comparison with two years of AERONET data gleaned from 133 AERONET stations. 8000 MODIS aerosol retrievals colocated with AERONET measurements confirm that one-standard deviation of MODIS optical thickness retrievals fall within the predicted uncertainty of delta tauapproximately equal to plus or minus 0.03 plus or minus 0.05 tau over ocean and delta tay equal to plus or minus 0.05 plus or minus 0.15 tau over land. 271 MODIS aerosol retrievals co-located with AERONET inversions at island and coastal sites suggest that one-standard deviation of MODIS effective radius retrievals falls within delta r_eff approximately equal to 0.11 microns. The accuracy of the MODIS retrievals suggests that the product can be used to help narrow the uncertainties associated with aerosol radiative forcing of global climate.

  20. MATRIX (Multiconfiguration Aerosol TRacker of mIXing state): an aerosol microphysical module for global atmospheric models

    NASA Astrophysics Data System (ADS)

    Bauer, S. E.; Wright, D.; Koch, D.; Lewis, E. R.; McGraw, R.; Chang, L.-S.; Schwartz, S. E.; Ruedy, R.

    2008-05-01

    A new aerosol microphysical module MATRIX, the Multiconfiguation Aerosol TRacker of mIXing state, and its application in the Goddard Institute for Space Studies (GISS) climate model (ModelE) is described. This module, which is based on the quadrature method of moments (QMOM), represents nucleation, condensation, coagulation, internal and external mixing, and cloud-drop activation and provides aerosol particle mass and number concentration and particle size information for up to 16 mixed-mode aerosol populations. Internal and external mixing among aerosol components sulfate, nitrate, ammonium, carbonaceous aerosols, dust and sea-salt particles are represented. The solubility of each aerosol mode, which is explicitly calculated based on its soluble and insoluble components, enables calculation of the dependence of cloud drop activation on the microphysical characterization of multiple soluble modes. A detailed model description and results of box-model simulations of various mode configurations are presented. The number concentration of aerosol particles activated to cloud drops depends on the mode configuration. Simulations on the global scale with the GISS climate model are evaluated against aircraft and station measurements of aerosol mass and number concentration and particle size. The model accurately captures the observed size distributions in the aitken and accumulation modes up to particle diameter 1 μm, in which sulfate, nitrate, black and organic carbon are predominantly located; however the model underestimates coarse-mode number concentration and size, especially in the marine environment.

  1. Modeling particle number concentrations along Interstate 10 in El Paso, Texas

    NASA Astrophysics Data System (ADS)

    Olvera, Hector A.; Jimenez, Omar; Provencio-Vasquez, Elias

    2014-12-01

    Annual average daily particle number concentrations around a highway were estimated with an atmospheric dispersion model and a land use regression model. The dispersion model was used to estimate particle concentrations along Interstate 10 at 98 locations within El Paso, Texas. This model employed annual averaged wind speed and annual average daily traffic counts as inputs. A land use regression model with vehicle kilometers traveled as the predictor variable was used to estimate local background concentrations away from the highway to adjust the near-highway concentration estimates. Estimated particle number concentrations ranged between 9.8 × 103 particles/cc and 1.3 × 105 particles/cc, and averaged 2.5 × 104 particles/cc (SE 421.0). Estimates were compared against values measured at seven sites located along I10 throughout the region. The average fractional error was 6% and ranged between -1% and -13% across sites. The largest bias of -13% was observed at a semi-rural site where traffic was lowest. The average bias amongst urban sites was 5%. The accuracy of the estimates depended primarily on the emission factor and the adjustment to local background conditions. An emission factor of 1.63 × 1014 particles/veh-km was based on a value proposed in the literature and adjusted with local measurements. The integration of the two modeling techniques ensured that the particle number concentrations estimates captured the impact of traffic along both the highway and arterial roadways. The performance and economical aspects of the two modeling techniques used in this study shows that producing particle concentration surfaces along major roadways would be feasible in urban regions where traffic and meteorological data are readily available.

  2. Modeling particle number concentrations along Interstate 10 in El Paso, Texas

    PubMed Central

    Olvera, Hector A.; Jimenez, Omar; Provencio-Vasquez, Elias

    2014-01-01

    Annual average daily particle number concentrations around a highway were estimated with an atmospheric dispersion model and a land use regression model. The dispersion model was used to estimate particle concentrations along Interstate 10 at 98 locations within El Paso, Texas. This model employed annual averaged wind speed and annual average daily traffic counts as inputs. A land use regression model with vehicle kilometers traveled as the predictor variable was used to estimate local background concentrations away from the highway to adjust the near-highway concentration estimates. Estimated particle number concentrations ranged between 9.8 × 103 particles/cc and 1.3 × 105 particles/cc, and averaged 2.5 × 104 particles/cc (SE 421.0). Estimates were compared against values measured at seven sites located along I10 throughout the region. The average fractional error was 6% and ranged between -1% and -13% across sites. The largest bias of -13% was observed at a semi-rural site where traffic was lowest. The average bias amongst urban sites was 5%. The accuracy of the estimates depended primarily on the emission factor and the adjustment to local background conditions. An emission factor of 1.63 × 1014 particles/veh-km was based on a value proposed in the literature and adjusted with local measurements. The integration of the two modeling techniques ensured that the particle number concentrations estimates captured the impact of traffic along both the highway and arterial roadways. The performance and economical aspects of the two modeling techniques used in this study shows that producing particle concentration surfaces along major roadways would be feasible in urban regions where traffic and meteorological data are readily available. PMID:25313294

  3. Modeling particle number concentrations along Interstate 10 in El Paso, Texas.

    PubMed

    Olvera, Hector A; Jimenez, Omar; Provencio-Vasquez, Elias

    2014-12-01

    Annual average daily particle number concentrations around a highway were estimated with an atmospheric dispersion model and a land use regression model. The dispersion model was used to estimate particle concentrations along Interstate 10 at 98 locations within El Paso, Texas. This model employed annual averaged wind speed and annual average daily traffic counts as inputs. A land use regression model with vehicle kilometers traveled as the predictor variable was used to estimate local background concentrations away from the highway to adjust the near-highway concentration estimates. Estimated particle number concentrations ranged between 9.8 × 10(3) particles/cc and 1.3 × 10(5) particles/cc, and averaged 2.5 × 10(4) particles/cc (SE 421.0). Estimates were compared against values measured at seven sites located along I10 throughout the region. The average fractional error was 6% and ranged between -1% and -13% across sites. The largest bias of -13% was observed at a semi-rural site where traffic was lowest. The average bias amongst urban sites was 5%. The accuracy of the estimates depended primarily on the emission factor and the adjustment to local background conditions. An emission factor of 1.63 × 10(14) particles/veh-km was based on a value proposed in the literature and adjusted with local measurements. The integration of the two modeling techniques ensured that the particle number concentrations estimates captured the impact of traffic along both the highway and arterial roadways. The performance and economical aspects of the two modeling techniques used in this study shows that producing particle concentration surfaces along major roadways would be feasible in urban regions where traffic and meteorological data are readily available.

  4. A System to Create Stable Nanoparticle Aerosols from Nanopowders

    PubMed Central

    Ding, Yaobo; Riediker, Michael

    2016-01-01

    Nanoparticle aerosols released from nanopowders in workplaces are associated with human exposure and health risks. We developed a novel system, requiring minimal amounts of test materials (min. 200 mg), for studying powder aerosolization behavior and aerosol properties. The aerosolization procedure follows the concept of the fluidized-bed process, but occurs in the modified volume of a V-shaped aerosol generator. The airborne particle number concentration is adjustable by controlling the air flow rate. The system supplied stable aerosol generation rates and particle size distributions over long periods (0.5-2 hr and possibly longer), which are important, for example, to study aerosol behavior, but also for toxicological studies. Strict adherence to the operating procedures during the aerosolization experiments ensures the generation of reproducible test results. The critical steps in the standard protocol are the preparation of the material and setup, and the aerosolization operations themselves. The system can be used for experiments requiring stable aerosol concentrations and may also be an alternative method for testing dustiness. The controlled aerosolization made possible with this setup occurs using energy inputs (may be characterized by aerosolization air velocity) that are within the ranges commonly found in occupational environments where nanomaterial powders are handled. This setup and its operating protocol are thus helpful for human exposure and risk assessment. PMID:27501179

  5. 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.

  6. 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.

  7. 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.

  8. Evaluation of indoor aerosol control devices and their effects on radon progeny concentrations. Revision

    SciTech Connect

    Sextro, R.G.; Offermann, F.J.; Nazaroff, W.W.; Nero, A.V.; Revzan, K.L.; Yater, J.

    1984-11-01

    Eleven portable air cleaning devices have been evaluated for control of indoor concentrations of respirable particles, and their concomitant effects on radon progeny concentrations have been investigated. The experiments were conducted in a room-size chamber using cigarette smoke and radon injection from an external source. Of the devices examined the electrostatic precipitators and extended surface filters had significant particle removal rates, while the particle removal rates for several small panel-filters, an ion-generator, and a pair of mixing fans were found to be essentially negligible. The evaluation of radon progeny control produced similar results; the air cleaners which were effective in removing particles were also effective in reducing radon progeny concentrations. At the low particle concentrations, deposition of the unattached radon progeny on room surfaces was found to be a significant removal mechanism. Deposition rates of attached and unattached progeny have been estimated from these data, and were used to calculate the equilibrium factors for total and unattached progeny concentrations as a function of particle concentration. While particle removal reduces total airborne radon progeny concentrations, the relative alpha decay dose to the lungs appears to change very little as the particle concentration decreases due to the greater radiological importance of unattached progeny.

  9. Source and Health Implication of Diurnal Atmospheric PM Mass and Number Concentrations

    NASA Astrophysics Data System (ADS)

    Li, W.; Olvera, H. A.; Garcia, J. H.; Pingitore, N. E.

    2007-12-01

    Exposure to atmospheric PM has been known to be associated with adverse health effects, decreased heart-rate variability, and respiratory and cardiopulmonary related morbidity and mortality. New evidence suggests that physical characteristics (mass, size, number, surface area, and morphology) of particles are strongly associated with mortality and morbidity through acute exposure. In particular, as reported in the literature, fine or ultrafine particles are more toxic than coarse particles on an equivalent mass basis while particles of less than 30 nm or greater than 2.5 um in diameter deposit more effectively (approximately 80 percent) in lung versus approximately 18 percent for particles in the range of 100 nm and 1 um. In addition, positive association has been observed between day to day variation in PM2.5 and hospital admissions, mortality and particle surface area, or particle number concentration and oxidative stress-induced DNA damage. This presentation shows the results of a study characterizing the physical properties of PM in El Paso, Texas. Diurnal PM mass concentration peaks previously observed at several other cities along the U.S.-Mexico border and elsewhere in the world were observed in El Paso. The hourly PM particle count varied from less than 10,000 particles/cm3 to greater than 80,000 particles/cm3 during the diurnal PM mass peaks. The total number of PM particles peaked in the morning and in the evening while the mode of the particle size changed from 20 nm to 50 nm, indicating different PM sources may be responsible for the mass and number concentrations and agglomeration of particles in the atmosphere during the day may possibly plays a role. A multivariate regression analysis was performed to correlate the PM mass and number concentrations to environmental variables. Real- time wind statistics were used in conjunction with traffic data at a nearby highway for identifying sources of the PM mass and number concentration peaks. Evaluation of

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

    NASA Astrophysics Data System (ADS)

    Kampf, C. J.; Corrigan, A. L.; Johnson, A. M.; Song, W.; Keronen, P.; Königstedt, R.; Williams, J.; Russell, L. M.; Petäjä, T.; Fischer, H.; Hoffmann, T.

    2012-07-01

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

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

    NASA Astrophysics Data System (ADS)

    Kampf, C. J.; Corrigan, A. L.; Johnson, A. M.; Song, W.; Keronen, P.; Königstedt, R.; Williams, J.; Russell, L. M.; Petäjä, T.; Fischer, H.; Hoffmann, T.

    2012-01-01

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

  12. 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

  13. Microphysical processing of aerosol particles in orographic clouds

    NASA Astrophysics Data System (ADS)

    Pousse-Nottelmann, S.; Zubler, E. M.; Lohmann, U.

    2015-01-01

    An explicit and detailed treatment of cloud-borne particles allowing for the consideration of aerosol cycling in clouds has been implemented in the regional weather forecast and climate model COSMO. The effects of aerosol scavenging, cloud microphysical processing and regeneration upon cloud evaporation on the aerosol population and on subsequent cloud formation are investigated. For this, two-dimensional idealized simulations of moist flow over two bell-shaped mountains were carried out varying the treatment of aerosol scavenging and regeneration processes for a warm-phase and a mixed-phase orographic cloud. The results allowed to identify different aerosol cycling mechanisms. In the simulated non-precipitating warm-phase cloud, aerosol mass is incorporated into cloud droplets by activation scavenging and released back to the atmosphere upon cloud droplet evaporation. In the mixed-phase cloud, a first cycle comprises cloud droplet activation and evaporation via the Wegener-Bergeron-Findeisen process. A second cycle includes below-cloud scavenging by precipitating snow particles and snow sublimation and is connected to the first cycle via the riming process which transfers aerosol mass from cloud droplets to snow flakes. In the simulated mixed-phase cloud, only a negligible part of the total aerosol mass is incorporated into ice crystals. Sedimenting snow flakes reaching the surface remove aerosol mass from the atmosphere. The results show that aerosol processing and regeneration lead to a vertical redistribution of aerosol mass and number. However, the processes not only impact the total aerosol number and mass, but also the shape of the aerosol size distributions by enhancing the internally mixed/soluble accumulation mode and generating coarse mode particles. Concerning subsequent cloud formation at the second mountain, accounting for aerosol processing and regeneration increases the cloud droplet number concentration with possible implications for the ice

  14. Microphysical processing of aerosol particles in orographic clouds

    NASA Astrophysics Data System (ADS)

    Pousse-Nottelmann, S.; Zubler, E. M.; Lohmann, U.

    2015-08-01

    An explicit and detailed treatment of cloud-borne particles allowing for the consideration of aerosol cycling in clouds has been implemented into COSMO-Model, the regional weather forecast and climate model of the Consortium for Small-scale Modeling (COSMO). The effects of aerosol scavenging, cloud microphysical processing and regeneration upon cloud evaporation on the aerosol population and on subsequent cloud formation are investigated. For this, two-dimensional idealized simulations of moist flow over two bell-shaped mountains were carried out varying the treatment of aerosol scavenging and regeneration processes for a warm-phase and a mixed-phase orographic cloud. The results allowed us to identify different aerosol cycling mechanisms. In the simulated non-precipitating warm-phase cloud, aerosol mass is incorporated into cloud droplets by activation scavenging and released back to the atmosphere upon cloud droplet evaporation. In the mixed-phase cloud, a first cycle comprises cloud droplet activation and evaporation via the Wegener-Bergeron-Findeisen (WBF) process. A second cycle includes below-cloud scavenging by precipitating snow particles and snow sublimation and is connected to the first cycle via the riming process which transfers aerosol mass from cloud droplets to snowflakes. In the simulated mixed-phase cloud, only a negligible part of the total aerosol mass is incorporated into ice crystals. Sedimenting snowflakes reaching the surface remove aerosol mass from the atmosphere. The results show that aerosol processing and regeneration lead to a vertical redistribution of aerosol mass and number. Thereby, the processes impact the total aerosol number and mass and additionally alter the shape of the aerosol size distributions by enhancing the internally mixed/soluble Aitken and accumulation mode and generating coarse-mode particles. Concerning subsequent cloud formation at the second mountain, accounting for aerosol processing and regeneration increases

  15. Impact of global climate change on ozone, particulate matter, and secondary organic aerosol concentrations in California: A model perturbation analysis

    NASA Astrophysics Data System (ADS)

    Horne, Jeremy R.; Dabdub, Donald

    2017-03-01

    Air quality simulations are performed to determine the impact of changes in future climate and emissions on regional air quality in the South Coast Air Basin (SoCAB) of California. The perturbation parameters considered in this study include (1) temperature, (2) absolute humidity, (3) biogenic VOC emissions due to temperature changes, and (4) boundary conditions. All parameters are first perturbed individually. In addition, the impact of simultaneously perturbing more than one parameter is analyzed. Air quality is simulated with meteorology representative of a summertime ozone pollution episode using both a baseline 2005 emissions inventory and a future emissions projection for the year 2023. Different locations within the modeling domain exhibit varying degrees of sensitivity to the perturbations considered. Afternoon domain wide average ozone concentrations are projected to increase by 13-18% as a result of changes in future climate and emissions. Afternoon increases at individual locations range from 10 to 36%. The change in afternoon particulate matter (PM) levels is a strong function of location in the basin, ranging from -7.1% to +4.7% when using 2005 emissions and -8.6% to +1.7% when using 2023 emissions. Afternoon secondary organic aerosol (SOA) concentrations for the entire domain are projected to decrease by over 15%, and the change in SOA levels is not a strong function of the emissions inventory utilized. Temperature increases play the dominant role in determining the overall impact on ozone, PM, and SOA concentrations in both the individual and combined perturbation scenarios.

  16. 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...

  17. The variation of nitric acid vapor and nitrate aerosol concentrations near the island of Hawaii

    SciTech Connect

    Lee, G.

    1992-01-01

    Anthropogenic emissions of nitrogen oxides (NO + NO[sub 2]) are estimated to be half of the global emissions to the atmosphere. To understand the effect of increasing anthropogenic reactive nitrogen inputs to the global atmosphere, one needs to monitor their long-term variations. This dissertation examines the variations of total nitrate (nitric acid vapor and nitrate aerosol) at the Mauna Loa Observatory (MLO), Hawaii. During the Mauna Loa Observatory Photochemistry Experiment (MLOPEX) in May, 1988, six different air types were identified at MLO with statistical analysis. They were: (1) volcano influenced air, (2) stratosphere-like air, (3) boundary-layer air with recent anthropogenic influence, (4) photochemical haze, (5) marine boundary-layer air, (6) well-aged and modified marine air. Samples that might be influenced by marine air or human activity from local islands were eliminated with three meterological criteria (wind direction, condensation nuclei, and dew point). To examine the negative sampling artifacts of nitric acid vapor due to ground loss, mixing ratio gradients with height were measured during August of 1991. The observed gradients of nitric acid vapor indicated that the long-term samplers at 8 m at MLO may underestimate the free tropospheric nitric acid vapor mixing ratio by about 20%. The three year mean and median of free tropospheric total nitrate during long-term measurements were 113 pptv and 93 pptv, respectively. Each year, the total nitrate mixing ratios at MLO during the spring and summer were increased by more than a factor of two higher than fall and winter. NO[sub y] from remote continents (Asia and North America) are likely sources of these increased total nitrate at MLO during these seasons. However, other processes govern the total nitrate mixing ratios, e.g., degree of mixing between free tropospheric air and boundary air at source regions, stratospheric injection, and wet removal of total nitrate.

  18. Biogenic sulfur emissions and aerosols over the tropical South Atlantic: 3. Atmospheric dimethylsulfide, aerosols and cloud condensation nuclei

    NASA Astrophysics Data System (ADS)

    Andreae, Meinrat O.; Elbert, Wolfgang; de Mora, Stephen J.

    1995-06-01

    We measured dimethylsulfide in air (DMSa) and the number concentration, size distribution, and chemical composition of atmospheric aerosols, including the concentration of cloud condensation nuclei (CCN), during February-March 1991 over the tropical South Atlantic along 19°S (F/S Meteor, cruise 15/3). Aerosol number/size distributions were determined with a laser-optical particle counter, condensation nuclei (CN) concentrations with a TSI 3020, and cloud condensation nuclei (CCN) with a Hudson-type supersaturation chamber. Aerosol samples were collected on two-stage stacked filters and analyzed by ion chromatography for soluble ion concentrations. Black carbon in aerosols was measured by visible light absorption and used to identify and eliminate periods with anthropogenic pollution from the data set. Meteorological analysis shows that most of the air masses sampled had spent extended periods over remote marine areas in the tropical and subtropical region. DMSa was closely correlated with the sea-to- air DMS flux calculated from DMS concentrations in seawater and meteorological data. Sea salt made the largest contribution to aerosol mass and volume but provided only a small fraction of the aerosol number concentration. The submicron aerosol had a mean composition close to ammonium bisulfate, with the addition of some methanesulfonate. Aerosol (CN and CCN) number and non-sea-salt sulfate concentrations were significantly correlated with DMS concentration and flux. This suggests that DMS oxidation followed by aerosol nucleation and growth in the marine boundary layer is an important, if not dominating, source of CN and possibly CCN. The degree of correlation between DMS and particle concentrations in the marine boundary layer may be strongly influenced by the different time scales of the processes regulating these concentrations. Our results provide strong support for several aspects of the CLAW hypothesis, which proposes the existence of a feedback loop linking DMS

  19. Detection of Free Tropospheric Air Masses With High So2 and Aerosol Concentrations: Evidence For New Aerosol Particle Formation By H2so4/h2o Nucleation

    NASA Astrophysics Data System (ADS)

    Katragkou, E.; Wilhelm, S.; Kiendler, A.; Arnold, F.; Minikin, A.; Schlager, H.; van Velthoven, P.

    Sulfur dioxide and aerosol measurements were performed in the free troposphere (FT) and the Planetary Boundary Layer (PBL) above continental Europe. The measure- ments took place on board of the German research aircraft "Falcon" in 18 April 2001 as a part of the SCAVEX campaign. A novel aircraft based CIMS (Chemical Ion- ization Mass Spectrometry) instrument equipped with an ion trap mass spectrometer (ITMS) with a low detection limit (50pptv) and a high time resolution (1.3s) operated by MPI-K was used to perform the SO2 measurements. For the aerosol measurements DLR-IPA operated a Condensation Particle Size Analyzer, detecting particles with diameters d > 4, 7, 9 and 20nm and a PCASP-100X aerosol spectrometer probe (d > 100nm). In the measurements made mostly around 5000m altitude SO2 rich air masses were occasionally observed with SO2 VMR of up to 2900pptv. The strong SO2 pollu- tion was due to fast vertical transport of polluted continental PBL air and small-scale deep convection, as indicated by the 5-day backward 3D trajectories. These observa- tions of strong SO2 pollution have interesting implications for aerosol processes, in- cluding efficient formation of gaseous sulfuric acid (GSA) and new aerosol particles. They also imply fast growth of freshly nucleated aerosol particles, which increases the chance for new particles to grow to the size of a CCN. Our analysis indicates the occurrence of new particle formation by H2SO4/H2O nucleation and fast new particle growth by H2SO4/H2O condensation and self-coagulation in the different air masses encountered during the flight.

  20. Automated Analysis of Human Sperm Number and Concentration (Oligospermia) Using Otsu Threshold Method and Labelling

    NASA Astrophysics Data System (ADS)

    Susrama, I. G.; Purnama, K. E.; Purnomo, M. H.

    2016-01-01

    Oligospermia is a male fertility issue defined as a low sperm concentration in the ejaculate. Normally the sperm concentration is 20-120 million/ml, while Oligospermia patients has sperm concentration less than 20 million/ml. Sperm test done in the fertility laboratory to determine oligospermia by checking fresh sperm according to WHO standards in 2010 [9]. The sperm seen in a microscope using a Neubauer improved counting chamber and manually count the number of sperm. In order to be counted automatically, this research made an automation system to analyse and count the sperm concentration called Automated Analysis of Sperm Concentration Counters (A2SC2) using Otsu threshold segmentation process and morphology. Data sperm used is the fresh sperm directly in the analysis in the laboratory from 10 people. The test results using A2SC2 method obtained an accuracy of 91%. Thus in this study, A2SC2 can be used to calculate the amount and concentration of sperm automatically

  1. Spatial and Temporal Variability of Outdoor Coarse Particulate Matter Mass Concentrations Measured with a New Coarse Particulate Sampler during the Detroit Exposure and Aerosol Research Study

    EPA Science Inventory

    The Detroit Exposure and Aerosol Research Study (DEARS) provided data to compare outdoor residential coarse particulate matter (PM10-2.5) concentrations in six different areas of Detroit with data from a central monitoring site. Daily and seasonal influences on the spa...

  2. MAPPING ANNUAL MEAN GROUND-LEVEL PM2.5 CONCENTRATIONS USING MULTIANGLE IMAGING SPECTRORADIOMETER AEROSOL OPTICAL THICKNESS OVER THE CONTIGUOUS UNITED STATES

    EPA Science Inventory

    We present a simple approach to estimating ground-level fine particle (PM2.5, particles smaller than 2.5 um in diameter) concentration using global atmospheric chemistry models and aerosol optical thickness (AOT) measurements from the Multi- angle Imaging SpectroRadiometer (MISR)...

  3. INDOOR/OUTDOOR AEROSOL CONCENTRATION RATIOS DURING THE 1999 FRESNO PARTICULATE MATTER EXPOSURE STUDIES AS A FUNCTION OF SIZE, SEASON, AND TIME OF DAY

    EPA Science Inventory

    The 1999 Fresno particulate matter exposure studies tools place in February (winter season) and April/May (spring season) for two periods of four weeks. During that time, near-continuous measurements of indoor and outdoor aerosol concentrations were made with a scanning mobilit...

  4. Elevated CO/sub 2/ concentration increases stomate numbers in phaseolus vulgaris leaves

    SciTech Connect

    O'Leary, J.W.; Knecht, G.N.

    1981-12-01

    Beans were grown under a constant CO/sub 2/ concentration of either 400 or 1200 ..mu..l liter/sup -1/. There was no significant difference in stomate density on the adaxial surface, but there was a significantly lower stomate density on the abaxial surface of leaves in the higher CO/sub 2/ concentration. The leaf area was significantly greater at the higher CO/sub 2/ concentration, and total number of stomates per leaf, calculated from the density and leaf area, was significantly greater for both surfaces of the leaf. We conclude that the observed CO/sub 2/ effect on stomatal density is the result of the large change in leaf area.

  5. Stratospheric aerosols and climatic change

    NASA Technical Reports Server (NTRS)

    Baldwin, B.; Pollack, J. B.; Summers, A.; Toon, O. B.; Sagan, C.; Van Camp, W.

    1976-01-01

    Generated primarily by volcanic explosions, a layer of submicron silicate particles and particles made of concentrated sulfuric acids solution is present in the stratosphere. Flights through the stratosphere may be a future source of stratospheric aerosols, since the effluent from supersonic transports contains sulfurous gases (which will be converted to H2SO4) while the exhaust from Space Shuttles contains tiny aluminum oxide particles. Global heat balance calculations have shown that the stratospheric aerosols have made important contributions to some climatic changes. In the present paper, accurate radiative transfer calculations of the globally-averaged surface temperature (T) are carried out to estimate the sensitivity of the climate to changes in the number of stratospheric aerosols. The results obtained for a specified model atmosphere, including a vertical profile of the aerosols, indicate that the climate is unlikely to be affected by supersonic transports and Space Shuttles, during the next decades.

  6. Black Carbon, Metal Concentrations and Lead Isotopes Ratios in Aerosols as Tracers of Human and Natural Activities in Northern Vietnam

    NASA Astrophysics Data System (ADS)

    Guinot, B. P.

    2015-12-01

    Atmospheric brown clouds (ABC) observed as widespread layers of brownish haze are regional scale plumes of air pollutants with a hot spot of emission located in East Asia. ABC are mainly composed of aerosol particles such as Black Carbon (BC) emitted to the atmosphere during biomass burning and fossil fuels combustion. The atmospheric lifetime of BC ranges from a few days in wet season up to one month in dry season. The use of stable lead isotopes and 21 elements as tracers of air pollution was applied to identify and characterized the main sources of anthropogenic activities in Asian region. Aerosol samples from Haiphong (North Vietnam) were collected by a high volume sampler for a period of one year from October 2012 to October 2013. Vietnam's 207Pb/206Pb ratios were almost identical to those found for China. Ratios of 207Pb/206Pb ranged from 0.837 to 0.871 which agrees with values previously reported for the last 10 years in China (0.841 - 0.879). No significant variation in isotope ratio was observed during the sampling period, which suggests that there was no large seasonal variation in the isotope ratios of airborne lead. Trajectory analysis showed that almost two third of the air masses originated from East Northeast which implies that China was a major source of lead in atmosphere. Enrichment factor calculations indicated a large influence of coal activity (EF(Al) As = 1982 ± 796, EF(Al) Cd = 972 ± 659, EF(Al) Sb = 1358 ± 930) but the difference between combustion and mining exploitation could not be evidenced. Significant correlations were found between two others groups of elements: As, Cu, Ni, Zn, and Al, Fe K, Co. Wind dilution was effective on metals concentration variation. During the cold and dry season (winter) ambient concentrations were high and variable, during the warm and wet season (summer) concentrations were stable and low. Taken together, these factors also identified industrial and lithogenic activities in the region.

  7. Optimized sparse-particle aerosol representations for modeling cloud-aerosol interactions

    NASA Astrophysics Data System (ADS)

    Fierce, Laura; McGraw, Robert

    2016-04-01

    Sparse representations of atmospheric aerosols are needed for efficient regional- and global-scale chemical transport models. Here we introduce a new framework for representing aerosol distributions, based on the method of moments. Given a set of moment constraints, we show how linear programming can be used to identify collections of sparse particles that approximately maximize distributional entropy. The collections of sparse particles derived from this approach reproduce CCN activity of the exact model aerosol distributions with high accuracy. Additionally, the linear programming techniques described in this study can be used to bound key aerosol properties, such as the number concentration of CCN. Unlike the commonly used sparse representations, such as modal and sectional schemes, the maximum-entropy moment-based approach is not constrained to pre-determined size bins or assumed distribution shapes. This study is a first step toward a new aerosol simulation scheme that will track multivariate aerosol distributions with sufficient computational efficiency for large-scale simulations.

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

    NASA Astrophysics Data System (ADS)

    Boucher, O.; Moulin, C.; Belviso, S.; Aumont, O.; Bopp, L.; Cosme, E.; von Kuhlmann, R.; Lawrence, M. G.; Pham, M.; Reddy, M. S.; Sciare, J.; Venkataraman, C.

    2003-01-01

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

  9. Size segregated mass concentration and size distribution of near surface aerosols over a tropical Indian semi-arid station, Anantapur: Impact of long range transport.

    PubMed

    Raghavendra Kumar, K; Narasimhulu, K; Balakrishnaiah, G; Suresh Kumar Reddy, B; Rama Gopal, K; Reddy, R R; Moorthy, K Krishna; Suresh Babu, S

    2009-10-15

    Regular measurements of size segregated as well as total mass concentration and size distribution of near surface composite aerosols, made using a ten-channel Quartz Crystal Microbalance (QCM) cascade impactor during the period of September 2007-May 2008 are used to study the aerosol characteristics in association with the synoptic meteorology. The total mass concentration varied from 59.70+/-1.48 to 41.40+/-1.72 microg m(-3), out of which accumulation mode dominated by approximately 50%. On a synoptic scale, aerosol mass concentration in the accumulation (submicron) mode gradually increased from an average low value of approximately 26.92+/-1.53 microg m(-3) during the post monsoon season (September-November) to approximately 34.95+/-1.32 microg m(-3) during winter (December-February) and reaching a peak value of approximately 43.56+/-1.42 microg m(-3) during the summer season (March-May). On the contrary, mass concentration of aerosols in the coarse (supermicron) mode increased from approximately 9.23+/-1.25 microg m(-3)during post monsoon season to reach a comparatively high value of approximately 25.89+/-1.95 microg m(-3) during dry winter months and a low value of approximately 8.07+/-0.76 microg m(-3) during the summer season. Effective radius, a parameter important in determining optical (scattering) properties of aerosol size distribution, varied between 0.104+/-0.08 microm and 0.167+/-0.06 microm with a mean value of 0.143+/-0.01 microm. The fine mode is highly reduced during the post monsoon period and the large and coarse modes continue to remain high (replenished) so that their relative dominance increases. It can be seen that among the two parameters measured, correlation of total mass concentration with air temperature is positive (R(2)=0.82) compared with relative humidity (RH) (R(2)=0.75).

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

    NASA Astrophysics Data System (ADS)

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

    2016-12-01

    Mineral dusts can have profound effects on climate, clouds, ecosystem processes, and human health. Because regional dust emission and deposition in western North America are not well understood, measurements of total suspended particulate (TSP) from 2011 to 2013 were made along a 500-km transect of five remote sites in Utah and Colorado, USA. The TSP concentrations in μg m-3 adjusted to a 24-h period were relatively high at the two westernmost, dryland sites at Canyonlands National Park (mean = 135) and at Mesa Verde National Park (mean = 99), as well as at the easternmost site on the Great Plains (mean = 143). The TSP concentrations at the two intervening montane sites were less, with more loading on the western slope of the Rocky Mountains (Telluride, mean = 68) closest to the desert sites compared with the site on the eastern slope (Niwot Ridge, mean = 58). Dust concentrations were commonly highest during late winter-late spring, when Pacific frontal storms are the dominant causes of regional wind. Low concentrations (<7 wt%) of organic matter indicated that rock-derived mineral particles composed most TSP. Most TSP mass was carried by particle sizes larger than 10 μm (PM>10), as revealed by relatively low average daily concentrations of fine (<5 μg m-3; PM2.5) and coarse (<10 μg m-3; PM2.5-10) fractions monitored at or near four sites. Standard air-quality measurements for PM2.5 and PM10 apparently do not capture the large majority of mineral-particulate pollution in the remote western interior U.S.

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

    USGS Publications Warehouse

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

    2016-01-01

    Mineral dusts can have profound effects on climate, clouds, ecosystem processes, and human health. Because regional dust emission and deposition in western North America are not well understood, measurements of total suspended particulate (TSP) from 2011 to 2013 were made along a 500-km transect of five remote sites in Utah and Colorado, USA. The TSP concentrations in μg m−3 adjusted to a 24-h period were relatively high at the two westernmost, dryland sites at Canyonlands National Park (mean = 135) and at Mesa Verde National Park (mean = 99), as well as at the easternmost site on the Great Plains (mean = 143). The TSP concentrations at the two intervening montane sites were less, with more loading on the western slope of the Rocky Mountains (Telluride, mean = 68) closest to the desert sites compared with the site on the eastern slope (Niwot Ridge, mean = 58). Dust concentrations were commonly highest during late winter-late spring, when Pacific frontal storms are the dominant causes of regional wind. Low concentrations (<7 wt%) of organic matter indicated that rock-derived mineral particles composed most TSP. Most TSP mass was carried by particle sizes larger than 10 μm (PM>10), as revealed by relatively low average daily concentrations of fine (<5 μg m−3; PM2.5) and coarse (<10 μg m−3; PM2.5–10) fractions monitored at or near four sites. Standard air-quality measurements for PM2.5 and PM10 apparently do not capture the large majority of mineral-particulate pollution in the remote western interior U.S.

  12. Aerosol and Trace Gas Sources in Northern China: Changes in Concentrations Before and After the Official "Heating Season" Help Characterize Emissions From Coal-Fired Boilers

    NASA Astrophysics Data System (ADS)

    Li, C.; Marufu, L. T.; Dickerson, R. R.; Li, Z.; Stehr, J. W.; Chen, H.; Wang, P.

    2006-05-01

    In March 2005, as a part of the project EAST-AIRE (East Asian Study of Tropospheric Aerosols: An International Regional Experiment), in-situ measurements of trace gases and aerosol optical properties were made at Xianghe, a rural surface site about 70 km east-southeast, generally downwind, of Beijing metropolitan area. CO, SO2, NO/NOy, O3, aerosol absorption coefficient, and aerosol scattering coefficients were determined simultaneously using the University of Maryland light aircraft instrument package. Pollutant ratios have been calculated to characterize the emission sources around the site. A dramatic drop in the NOy/CO ratio found around March 13/14 suggesting a sudden shutoff of a large fraction of the high- temperature combustion sources in the region. This observed change in concentrations occurred simultaneously with the transition from "heating season" to "non-heating season" in Northern China. Over the course of just a few days (around March 15), all boilers used to provide heat for cities and towns in this region are shut down in accordance with a governmental guideline. Most of these boilers operate with coal, and by using ratios of NOy/CO, SO2/CO, aerosol scattering/CO, and aerosol absorption/CO during and after the "heating season", emissions from these small to medium sized coal-fired boilers can be characterized. Results indicate that these residential and small-scale industrial heaters are a major source of NOy and SO2. Besides elevating the regional atmospheric pollutant level, the trace gases and aerosols emitted also have potential effects in other aspects such as the biogeochemical cycle of N and the agricultural production in this region.

  13. MATRIX (Multiconfiguration Aerosol TRacker of mIXing state): an aerosol microphysical module for global atmospheric models

    NASA Astrophysics Data System (ADS)

    Bauer, S. E.; Wright, D. L.; Koch, D.; Lewis, E. R.; McGraw, R.; Chang, L.-S.; Schwartz, S. E.; Ruedy, R.

    2008-10-01

    A new aerosol microphysical module MATRIX, the Multiconfiguration Aerosol TRacker of mIXing state, and its application in the Goddard Institute for Space Studies (GISS) climate model (ModelE) are described. This module, which is based on the quadrature method of moments (QMOM), represents nucleation, condensation, coagulation, internal and external mixing, and cloud-drop activation and provides aerosol particle mass and number concentration and particle size information for up to 16 mixed-mode aerosol populations. Internal and external mixing among aerosol components sulfate, nitrate, ammonium, carbonaceous aerosols, dust and sea-salt particles are represented. The solubility of each aerosol population, which is explicitly calculated based on its soluble and insoluble components, enables calculation of the dependence of cloud drop activation on the microphysical characterization of multiple soluble aerosol populations. A detailed model description and results of box-model simulations of various aerosol population configurations are presented. The box model experiments demonstrate the dependence of cloud activating aerosol number concentration on the aerosol population configuration; comparisons to sectional models are quite favorable. MATRIX is incorporated into the GISS climate model and simulations are carried out primarily to assess its performance/efficiency for global-scale atmospheric model application. Simulation results were compared with aircraft and station measurements of aerosol mass and number concentration and particle size to assess the ability of the new method to yield data suitable for such comparison. The model accurately captures the observed size distributions in the Aitken and accumulation modes up to particle diameter 1 μm, in which sulfate, nitrate, black and organic carbon are predominantly located; however the model underestimates coarse-mode number concentration and size, especially in the marine environment. This is more likely due to

  14. Relationships between number, surface area, and mass concentrations of different nanoparticles in workplaces.

    PubMed

    Zou, Hua; Zhang, Qunwei; Xing, Mingluan; Gao, Xiangjing; Zhou, Lifang; Tollerud, David J; Tang, Shichuang; Zhang, Meibian

    2015-08-01

    No consistent metric for measuring exposure to nanoparticles has yet been agreed upon internationally. This study seeks to examine the relationship between the number concentration (NC), surface area concentration (SAC), and mass concentration (MC) of nanoparticles in workplaces. Real-time NC20-1000 nm, SAC10-1000 nm, and respirable MC100-1000 nm were determined for different nanoparticles. Concentration ratio (CR, activity: background), exposure ranking (ER), and between-metric correlation coefficients (R) were used to analyze the relationships between the three metrics. The ratio of cumulative percentage by number (APN) and cumulative percentage by mass (APM) was used to analyze whether the nanoparticle number is predominant, as compared with the nanoparticle mass. The CRs of NC20-1000 nm and SAC10-1000 nm for different nanoparticles at the corresponding work sites were higher than those of respirable MC100-1000 nm. The ERs of NC20-1000 nm for nano-Fe2O3 and nano-Al2O3 were the same as those of SAC10-1000 nm, but were inconsistent with those of respirable MC100-1000 nm. The order of correlation coefficients between NC20-1000 nm, SAC10-1000 nm, and respirable MC100-1000 nm was: RSAC and NC > RSAC and MC > RNC and MC. The ratios of APN and APM for nano-Al2O3 and grinding-wheel particles (less than 100 nm) at the same work site were 2.03 and 1.65, respectively. NC and SAC metrics are significantly distinct from the MC in characterizing exposure to airborne nanoparticles. Simultaneous measurements of the NC, SAC, and MC should be conducted as part of nanoparticle exposure assessment strategies and epidemiological studies.

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

    NASA Astrophysics Data System (ADS)

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

    2015-07-01

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

  16. Measured In Situ Atmospheric Ambient Aerosol Size-Distributions, Particle Concentrations, and Turbulence Data for RSA TA-6 Test Range, Redstone Arsenal, AL, April-May 2015

    DTIC Science & Technology

    2015-09-01

    Concentrations, and Turbulence Data for RSA TA-6 Test Range, Redstone Arsenal , AL, April–May 2015 by Kristan Gurton, Stephanie Cunningham, and...Aerosol Size-Distributions, Particle Concentrations, and Turbulence Data for RSA TA-6 Test Range, Redstone Arsenal , AL, April–May 2015 by Kristan...Redstone Arsenal , AL Approved for public release; distribution unlimited. ii REPORT DOCUMENTATION PAGE Form Approved OMB No. 0704-0188

  17. Local emission of primary air pollutants and its contribution to wet deposition and concentrations of aerosols and gases in ambient air in Japan

    NASA Astrophysics Data System (ADS)

    Aikawa, Masahide; Hiraki, Takatoshi; Tomoyose, Nobutaka; Ohizumi, Tsuyoshi; Noguchi, Izumi; Murano, Kentaro; Mukai, Hitoshi

    2013-11-01

    We studied wet deposition by precipitation and the concentrations of aerosols and gases in ambient air in relation to the primary air pollutants discharged from domestic areas. The concentrations of aerosols and gases were influenced by nearby emissions except for non-sea-salt SO, which is transported long distances. The area facing the Sea of Japan showed much larger wet deposition than other areas, although the domestic emissions of the primary air pollutants there were small and showed a peak in wet deposition from October to March, as distinct from April to September in other areas. We performed the correlation analyses between wet deposition of each component and the product of the concentrations of corresponding aerosols and gases in ambient air and the two-thirds power of the precipitation. From the results, following scavenging processes were suggested. • Sulfate and ammonium were scavenged in precipitation as particulate matter such as (NH4)2SO4 and NH4HSO4. • Nitrate was scavenged mainly in precipitation through gaseous HNO3. • Ammonium was complementarily scavenged in precipitation through aerosols such as (NH4)2SO4 and NH4HSO4 and through gaseous NH3.

  18. The effects of vegetation barriers on near-road ultrafine particle number and carbon monoxide concentrations.

    PubMed

    Lin, Ming-Yeng; Hagler, Gayle; Baldauf, Richard; Isakov, Vlad; Lin, Hong-Yiou; Khlystov, Andrey

    2016-05-15

    Numerous studies have shown that people living in near-roadway communities (within 100 m of the road) are exposed to high ultrafine particle (UFP) number concentrations, which may be associated with adverse health effects. Vegetation barriers have been shown to affect pollutant transport via particle deposition to leaves and altering the dispersion of emission plumes, which in turn would modify the exposure of near-roadway communities to traffic-related UFPs. In this study, both stationary (equipped with a Scanning Mobility Particle Sizer, SMPS) and mobile (equipped with Fast Mobility Particle Sizer, FMPS) measurements were conducted to investigate the effects of vegetation barriers on downwind UFP (particle diameters ranging from 14 to 102 nm) concentrations at two sites in North Carolina, USA. One site had mainly deciduous vegetation while the other was primarily coniferous; both sites have a nearby open field without the vegetation barriers along the same stretch of limited access road, which served as a reference. During downwind conditions (traffic emissions transported towards the vegetation barrier) and when the wind speed was above or equal to 0.5m/s, field measurements indicated that vegetation barriers with full foliage reduced UFP and CO concentrations by 37.7-63.6% and 23.6-56.1%, respectively. When the test was repeated at the same sites during winter periods when deciduous foliage was reduced, the deciduous barrier during winter showed no significant change in UFP concentration before and after the barrier. Results from the stationary (using SMPS) and mobile (using FMPS) measurements for UFP total number concentrations generally agreed to within 20%.

  19. Comparison of Bulk Carbon Concentrations and Optical Properties of Carbonaceous Aerosols in the North Slope Alaska from Summer 2012 and Summer 2015

    NASA Astrophysics Data System (ADS)

    Sheesley, R. J.; Barrett, T. E.; Moffett, C.; Gunsch, M.; Pratt, K.

    2015-12-01

    With recent drilling permits being issued for exploratory drilling in the Chukchi Sea, there is a need for characterization of carbonaceous aerosols in the Arctic both prior to and during the exploratory drilling phase. A month-long field sampling campaign will be conducted in Barrow, AK, at the confluence of the Chukchi and Beaufort seas, from August to September 2015. Total suspended particulate (TSP) aerosol samples will be collected at the Department of Energy Atmospheric Radiation Measurement (ARM) climate research facility in Barrow, AK, USA. Samples will be analyzed for organic carbon (OC), elemental carbon (EC) on a Sunset carbon analyzer utilizing the NIOSH 5040 method. Samples will also be analyzed for water soluble organic carbon (WSOC) using a water extraction method and subsequent analysis on a Shimadzu Total Carbon Analyzer. Optical properties of the aqueous extracts will also be measured using an Agilent ultraviolet-visible (UV-Vis) spectrometer. OC, EC and WSOC concentrations will then be compared to aerosol samples collected at the same location in summer 2012, prior to the onset of exploratory drilling in the Chukchi Sea. Back trajectory (BT) analysis will be performed for each sampling campaign to help assess the impact of source region on the carbonaceous aerosol budget and to identify any changes in source region between the two campaigns. A comparison of samples from the same location and season both prior to and post drilling will allow for a more accurate characterization and tracking of the potential impacts of new aerosol emission sources in the region.

  20. Comparison of MADE3-simulated and observed aerosol distributions with a focus on aerosol vertical profiles

    NASA Astrophysics Data System (ADS)

    Kaiser, Christopher; Hendricks, Johannes; Righi, Mattia; Jöckel, Patrick

    2016-04-01

    The reliability of aerosol radiative forcing estimates from climate models depends on the accuracy of simulated global aerosol distribution and composition, as well as on the models' representation of the aerosol-cloud and aerosol-radiation interactions. To help improve on previous modeling studies, we recently developed the new aerosol microphysics submodel MADE3 that explicitly tracks particle mixing state in the Aitken, accumulation, and coarse mode size ranges. We implemented MADE3 into the global atmospheric chemistry general circulation model EMAC and evaluated it by comparison of simulated aerosol properties to observations. Compared properties include continental near-surface aerosol component concentrations and size distributions, continental and marine aerosol vertical profiles, and nearly global aerosol optical depth. Recent studies have shown the specific importance of aerosol vertical profiles for determination of the aerosol radiative forcing. Therefore, our focus here is on the evaluation of simulated vertical profiles. The observational data is taken from campaigns between 1990 and 2011 over the Pacific Ocean, over North and South America, and over Europe. The datasets include black carbon and total aerosol mass mixing ratios, as well as aerosol particle number concentrations. Compared to other models, EMAC with MADE3 yields good agreement with the observations - despite a general high bias of the simulated mass mixing ratio profiles. However, BC concentrations are generally overestimated by many models in the upper troposphere. With MADE3 in EMAC, we find better agreement of the simulated BC profiles with HIPPO data than the multi-model average of the models that took part in the AeroCom project. There is an interesting difference between the profiles from individual campaigns and more "climatological" datasets. For instance, compared to spatially and temporally localized campaigns, the model simulates a more continuous decline in both total

  1. 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.

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

    USGS Publications Warehouse

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

    2014-01-01

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

  3. The effect of dry and wet deposition of condensable vapors on secondary organic aerosols concentrations over the continental US

    NASA Astrophysics Data System (ADS)

    Knote, C.; Hodzic, A.; Jimenez, J. L.

    2015-01-01

    The effect of dry and wet deposition of semi-volatile organic compounds (SVOCs) in the gas phase on the concentrations of secondary organic aerosol (SOA) is reassessed using recently derived water solubility information. The water solubility of SVOCs was implemented as a function of their volatility distribution within the WRF-Chem regional chemistry transport model, and simulations were carried out over the continental United States for the year 2010. Results show that including dry and wet removal of gas-phase SVOCs reduces annual average surface concentrations of anthropogenic and biogenic SOA by 48 and 63% respectively over the continental US. Dry deposition of gas-phase SVOCs is found to be more effective than wet deposition in reducing SOA concentrations (-40 vs. -8% for anthropogenics, and -52 vs. -11% for biogenics). Reductions for biogenic SOA are found to be higher due to the higher water solubility of biogenic SVOCs. The majority of the total mass of SVOC + SOA is actually deposited via the gas phase (61% for anthropogenics and 76% for biogenics). Results are sensitive to assumptions made in the dry deposition scheme, but gas-phase deposition of SVOCs remains crucial even under conservative estimates. Considering reactivity of gas-phase SVOCs in the dry deposition scheme was found to be negligible. Further sensitivity studies where we reduce the volatility of organic matter show that consideration of gas-phase SVOC removal still reduces average SOA concentrations by 31% on average. We consider this a lower bound for the effect of gas-phase SVOC removal on SOA concentrations. A saturation effect is observed for Henry's law constants above 108 M atm-1, suggesting an upper bound of reductions in surface level SOA concentrations by 60% through removal of gas-phase SVOCs. Other models that do not consider dry and wet removal of gas-phase SVOCs would hence overestimate SOA concentrations by roughly 50%. Assumptions about the water solubility of SVOCs made in

  4. The effect of dry and wet deposition of condensable vapors on secondary organic aerosols concentrations over the continental US

    DOE PAGES

    Knote, C.; Hodzic, A.; Jimenez, J. L.

    2015-01-06

    The effect of dry and wet deposition of semi-volatile organic compounds (SVOCs) in the gas phase on the concentrations of secondary organic aerosol (SOA) is reassessed using recently derived water solubility information. The water solubility of SVOCs was implemented as a function of their volatility distribution within the WRF-Chem regional chemistry transport model, and simulations were carried out over the continental United States for the year 2010. Results show that including dry and wet removal of gas-phase SVOCs reduces annual average surface concentrations of anthropogenic and biogenic SOA by 48 and 63% respectively over the continental US. Dry deposition ofmore » gas-phase SVOCs is found to be more effective than wet deposition in reducing SOA concentrations (−40 vs. −8% for anthropogenics, and −52 vs. −11% for biogenics). Reductions for biogenic SOA are found to be higher due to the higher water solubility of biogenic SVOCs. The majority of the total mass of SVOC + SOA is actually deposited via the gas phase (61% for anthropogenics and 76% for biogenics). Results are sensitive to assumptions made in the dry deposition scheme, but gas-phase deposition of SVOCs remains crucial even under conservative estimates. Considering reactivity of gas-phase SVOCs in the dry deposition scheme was found to be negligible. Further sensitivity studies where we reduce the volatility of organic matter show that consideration of gas-phase SVOC removal still reduces average SOA concentrations by 31% on average. We consider this a lower bound for the effect of gas-phase SVOC removal on SOA concentrations. A saturation effect is observed for Henry's law constants above 108 M atm−1, suggesting an upper bound of reductions in surface level SOA concentrations by 60% through removal of gas-phase SVOCs. Other models that do not consider dry and wet removal of gas-phase SVOCs would hence overestimate SOA concentrations by roughly 50%. Assumptions about the water solubility

  5. Atmospheric trace metals over the Atlantic and South Indian Oceans: Investigation of metal concentrations and lead isotope ratios in coastal and remote marine aerosols

    NASA Astrophysics Data System (ADS)

    Witt, Melanie; Baker, Alex R.; Jickells, Tim D.

    Atmospheric concentrations of trace metals over the oceans are investigated through analysis of aerosol samples collected during cruises from the UK to the Falkland Islands and from South Africa to Australia. The readily soluble concentrations of Cu (4-256 pmol m -3), Ni (0.1-54 pmol m -3), Ba (0.2-60 pmol m -3), Zn (6-316 pmol m -3), Cd (0.01-0.29 pmol m -3) and Pb (0.4-22 pmol m -3) were measured in the aerosols, along with total concentrations of crustal elements (Fe, Al and Mn) to evaluate the crustal contributions. Air mass back trajectories suggested most of the aerosol samples had spent several days over the ocean prior to collection. The highest metal concentrations were observed in aerosols close to South Africa, Australia and major cities in South America, although these concentrations were lower than had been reported previously in the literature. Apart from Ba, which had a major crustal source, the trace metals were enriched relative to crustal sources in most samples, including some collected thousands of kilometers from emission sources. The mean trace metal concentrations in the remote Indian Ocean were lower than those measured in the Atlantic Ocean. Even lower concentrations are reported in the literature for the remote Pacific Ocean. In contrast to previous studies, no clear north-south gradient is observed in the concentrations of the trace metals in the aerosols. Lead isotope measurements were also carried out on aerosol samples using a multicollector inductively coupled plasma mass spectrometer to assist in source apportionment. Clear differences were noted in the isotope ratios collected on either side of the Indian Ocean with Australian lead ore dominating over much of the eastern and mid-southern Indian Ocean. Samples collected over the western Indian Ocean and Atlantic Ocean under South African influence had lead isotopes quite different from those seen in South African cities in the past, and are closer in ratio to the coal signature of

  6. Influence of manufacturer lot number on pharmacokinetic manipulation of gentamicin serum concentrations.

    PubMed

    Gill, M A; Kern, J W; Chenella, F C; Berne, T V; Heseltine, P N; Yellin, A E

    1983-01-01

    A prospective, randomized trial was performed to study the impact of lot variation on pharmacokinetic manipulation of serum gentamicin concentrations. Twenty patients receiving gentamicin were randomized prospectively into two groups. Group I patients had blood samples obtained before and after two doses during their hospital regimen using gentamicin from the same lot number. Group II patients had the samples obtained around two doses using different lot numbers of gentamicin. Pharmacokinetic parameters were calculated assuming a one-compartment model and were compared between the initial and subsequent set of serum concentrations. For Group I, the gentamicin distribution volume (Vd) did not differ (mean change, -0.007 L/kg, or mean absolute percentage change, 20.8%). Group II also did not have a significant mean change in Vd (0.023 L/kg, or mean absolute percentage change, 18.7%). The gentamicin Vd did not appear to change over time whether gentamicin was administered using identical or differing lot numbers.

  7. Comparison of two direct-reading instruments (FM-7400 and Fibrecheck FC-2) with phase contrast optical microscopy to measure the airborne fibre number concentration.

    PubMed

    Kauffer, E; Martin, P; Grzebyk, M; Villa, M; Vigneron, J C

    2003-07-01

    The use of direct-reading instruments to measure the airborne fibre number concentration is on the increase. The response of two of these instruments (FM-7400 and Fibrecheck FC-2) was compared with the conventional method of sampling on filters and counting by phase contrast microscopy. Four types of fibres were studied at different concentrations and relative humidity levels. The FM-7400 can be calibrated by the manufacturer for two different levels of sensitivity (standard and high). For the tests where it was set to the sensitivity level with which it had been calibrated, the ratio of the concentration measured by the instrument to the concentration obtained by the conventional method varied in the range 0.5-1 for the different types of fibres studied (chrysotile, glass wool and ceramic fibres). The Fibrecheck FC-2 is a much less versatile instrument. On the basis of a calibration allowing correct detection of asbestos fibres, it greatly overestimated the concentration of man-made mineral fibres. In its normal calibration state a fine chrysotile aerosol was poorly detected. For man-made mineral fibres, the response was highly dependent on the nature of the fibres. These instruments require calibration with the type of fibres to be studied. Unfortunately, this operation is not always accessible to the user and may require the services of a specialized laboratory, as the manufacturer is not always in a position to carry this out.

  8. 40 CFR Table C-1 to Subpart C of... - Test Concentration Ranges, Number of Measurements Required, and Maximum Discrepancy Specifications

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 6 2012-07-01 2012-07-01 false Test Concentration Ranges, Number of... Reference Methods Pt. 53, Subpt. C, Table C-1 Table C-1 to Subpart C of Part 53—Test Concentration Ranges, Number of Measurements Required, and Maximum Discrepancy Specifications Pollutant Concentration...

  9. 40 CFR Table C-1 to Subpart C of... - Test Concentration Ranges, Number of Measurements Required, and Maximum Discrepancy Specifications

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 5 2011-07-01 2011-07-01 false Test Concentration Ranges, Number of... Reference Methods Pt. 53, Subpt. C, Table C-1 Table C-1 to Subpart C of Part 53—Test Concentration Ranges, Number of Measurements Required, and Maximum Discrepancy Specifications Pollutant Concentration...

  10. 40 CFR Table C-1 to Subpart C of... - Test Concentration Ranges, Number of Measurements Required, and Maximum Discrepancy Specifications

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 6 2014-07-01 2014-07-01 false Test Concentration Ranges, Number of... Reference Methods Pt. 53, Subpt. C, Table C-1 Table C-1 to Subpart C of Part 53—Test Concentration Ranges, Number of Measurements Required, and Maximum Discrepancy Specifications Pollutant Concentration...

  11. 40 CFR Table C-1 to Subpart C of... - Test Concentration Ranges, Number of Measurements Required, and Maximum Discrepancy Specifications

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 6 2013-07-01 2013-07-01 false Test Concentration Ranges, Number of... Reference Methods Pt. 53, Subpt. C, Table C-1 Table C-1 to Subpart C of Part 53—Test Concentration Ranges, Number of Measurements Required, and Maximum Discrepancy Specifications Pollutant Concentration...

  12. Size distributions of fine and ultrafine particles in the city of Strasbourg: correlation between number of particles and concentrations of NO(x) and SO(2) gases and some soluble ions concentration determination.

    PubMed

    Roth, Estelle; Kehrli, Damaris; Bonnot, Karine; Trouvé, Gwénaëlle

    2008-01-01

    An Electrical Low Pressure Impactor (ELPI) was used during spring and autumn 2003 in the centre of Strasbourg for the measurement of atmospheric aerosols size distribution. The concentration of NO(x) and SO(2) in air was simultaneously measured with specific analysers. Samples were collected in the range 0.007-10 microm in equivalent aerodynamic diameter size. Number distributions are representative of a pollution originating from urban traffic with a particle size distribution exhibiting a nucleation mode below 29 nm and an accumulation mode around 80 nm in size. A mean particle density equal to 39000+/-35000 total particles per cm(3) with a size ranging from 7 to 10 microm was obtained after a sampling period of 2 weeks in spring. About 86.9% of the number of particles have an aerodynamic diameter below 0.1 microm and 13.1% between 0.1 and 1 microm. Correlation coefficients between the number of particles impacted on each ELPI plate and gas concentrations (SO(2) and NO(x)) showed that the numbers of particles with diameter between 0.10 and 0.62 microm are highly related to the NO(x) concentration. This result indicates that particles are traffic induced since NO(x) is mainly emitted by cars as shown by measurements on various sites. Particles are less clearly correlated to the SO(2) concentration. Particle analysis on different ELPI plates for a sampling period of 2 weeks in autumn showed high level of soluble NO(3)(-), SO(4)(2-) and NH(4)(+) ions. Indeed, up to 90% b.w. of these three species were found in the particle range 0.1-1 microm. The formation of particulate NH(4)NO(3) is favoured by high NO(x) concentration, which induces the formation of gaseous HNO(3).

  13. 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.

  14. Impact of aerosol size representation on modeling aerosol-cloud interactions

    DOE PAGES

    Zhang, Y.; Easter, R. C.; Ghan, S. J.; ...

    2002-11-07

    In this study, we use a 1-D version of a climate-aerosol-chemistry model with both modal and sectional aerosol size representations to evaluate the impact of aerosol size representation on modeling aerosol-cloud interactions in shallow stratiform clouds observed during the 2nd Aerosol Characterization Experiment. Both the modal (with prognostic aerosol number and mass or prognostic aerosol number, surface area and mass, referred to as the Modal-NM and Modal-NSM) and the sectional approaches (with 12 and 36 sections) predict total number and mass for interstitial and activated particles that are generally within several percent of references from a high resolution 108-section approach.more » The modal approach with prognostic aerosol mass but diagnostic number (referred to as the Modal-M) cannot accurately predict the total particle number and surface areas, with deviations from the references ranging from 7-161%. The particle size distributions are sensitive to size representations, with normalized absolute differences of up to 12% and 37% for the 36- and 12-section approaches, and 30%, 39%, and 179% for the Modal-NSM, Modal-NM, and Modal-M, respectively. For the Modal-NSM and Modal-NM, differences from the references are primarily due to the inherent assumptions and limitations of the modal approach. In particular, they cannot resolve the abrupt size transition between the interstitial and activated aerosol fractions. For the 12- and 36-section approaches, differences are largely due to limitations of the parameterized activation for non-log-normal size distributions, plus the coarse resolution for the 12-section case. Differences are larger both with higher aerosol (i.e., less complete activation) and higher SO2 concentrations (i.e., greater modification of the initial aerosol distribution).« less

  15. Impact of aerosol size representation on modeling aerosol-cloud interactions

    SciTech Connect

    Zhang, Y.; Easter, R. C.; Ghan, S. J.; Abdul-Razzak, H.

    2002-11-07

    In this study, we use a 1-D version of a climate-aerosol-chemistry model with both modal and sectional aerosol size representations to evaluate the impact of aerosol size representation on modeling aerosol-cloud interactions in shallow stratiform clouds observed during the 2nd Aerosol Characterization Experiment. Both the modal (with prognostic aerosol number and mass or prognostic aerosol number, surface area and mass, referred to as the Modal-NM and Modal-NSM) and the sectional approaches (with 12 and 36 sections) predict total number and mass for interstitial and activated particles that are generally within several percent of references from a high resolution 108-section approach. The modal approach with prognostic aerosol mass but diagnostic number (referred to as the Modal-M) cannot accurately predict the total particle number and surface areas, with deviations from the references ranging from 7-161%. The particle size distributions are sensitive to size representations, with normalized absolute differences of up to 12% and 37% for the 36- and 12-section approaches, and 30%, 39%, and 179% for the Modal-NSM, Modal-NM, and Modal-M, respectively. For the Modal-NSM and Modal-NM, differences from the references are primarily due to the inherent assumptions and limitations of the modal approach. In particular, they cannot resolve the abrupt size transition between the interstitial and activated aerosol fractions. For the 12- and 36-section approaches, differences are largely due to limitations of the parameterized activation for non-log-normal size distributions, plus the coarse resolution for the 12-section case. Differences are larger both with higher aerosol (i.e., less complete activation) and higher SO2 concentrations (i.e., greater modification of the initial aerosol distribution).

  16. Characteristics of Ambient Black Carbon Mass and Size-Resolved Particle Number Concentrations during Corn Straw Open-Field Burning Episode Observations at a Rural Site in Southern Taiwan.

    PubMed

    Cheng, Yu-Hsiang; Yang, Li-Sing

    2016-07-08

    Information on the effect of open-field burning of agricultural residues on ambient black carbon (BC) mass and size-resolved particle number concentrations is scarce. In this study, to understand the effect of such open-field burning on short-term air quality, real-time variations of the BC mass and size-resolved particle number concentrations were monitored before and during a corn straw open-field burning episode at a rural site. Correlations between the BC mass and size-resolved particle number concentrations during the episode were investigated. Moreover, the particle number size distribution and absorption Ångström exponent were determined for obtaining the characteristics of aerosol emissions from the corn straw open-field burning. The results can be used to address public health concerns and as a reference for managing similar episodes of open-field burning of agricultural residues.

  17. Characteristics of Ambient Black Carbon Mass and Size-Resolved Particle Number Concentrations during Corn Straw Open-Field Burning Episode Observations at a Rural Site in Southern Taiwan

    PubMed Central

    Cheng, Yu-Hsiang; Yang, Li-Sing

    2016-01-01

    Information on the effect of open-field burning of agricultural residues on ambient black carbon (BC) mass and size-resolved particle number concentrations is scarce. In this study, to understand the effect of such open-field burning on short-term air quality, real-time variations of the BC mass and size-resolved particle number concentrations were monitored before and during a corn straw open-field burning episode at a rural site. Correlations between the BC mass and size-resolved particle number concentrations during the episode were investigated. Moreover, the particle number size distribution and absorption Ångström exponent were determined for obtaining the characteristics of aerosol emissions from the corn straw open-field burning. The results can be used to address public health concerns and as a reference for managing similar episodes of open-field burning of agricultural residues. PMID:27399754

  18. Aerosol activation properties and CCN closure during TCAP

    NASA Astrophysics Data System (ADS)

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

    2013-12-01

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

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

    NASA Astrophysics Data System (ADS)

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

    2013-04-01

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

  20. High concentrations of biological aerosol particles and ice nuclei during and after rain

    NASA Astrophysics Data System (ADS)

    Huffman, J. A.; Pöhlker, C.; Prenni, A. J.; DeMott, P. J.; Mason, R. H.; Robinson, N. H.; Fröhlich-Nowoisky, J.; Tobo, Y.; Després, V. R.; Garcia, E.; Gochis, D. J.; Harris, E.; Müller-Germann, I.; Ruzene, C.; Schmer, B.; Sinha, B.; Day, D. A.; Andreae, M. O.; Jimenez, J. L.; Gallagher, M.; Kreidenweis, S. M.; Bertram, A. K.; Pöschl, U.

    2013-01-01

    Bioaerosols are relevant for public health and may play an important role in the climate system, but their atmospheric abundance, properties and sources are not well understood. Here we show that the concentration of airborne biological particles in a forest ecosystem increases dramatically during rain and that bioparticles are closely correlated with atmospheric ice nuclei (IN). The greatest increase of bioparticles and IN occurred in the size range of 2-6 μm, which is characteristic for bacterial aggregates and fungal spores. By DNA analysis we found high diversities of airborne bacteria and fungi, including human and plant pathogens (mildew, smut and rust fungi, molds, Enterobacteraceae, Pseudomonadaceae). In addition to known bacterial and fungal IN (Pseudomonas sp., Fusarium sporotrichioides), we discovered two species of IN-active fungi that were not previously known as biological ice nucleators (Isaria farinosa and Acremonium implicatum). Our findings suggest that atmospheric bioaerosols, IN and rainfall are more tightly coupled than previously assumed.

  1. High concentrations of biological aerosol particles and ice nuclei during and after rain

    NASA Astrophysics Data System (ADS)

    Huffman, J. Alex; Pöhlker, Christopher; Prenni, Anthony; DeMott, Paul; Mason, Ryan; Robinson, Niall; Fröhlich-Nowoisky, Janine; Tobo, Yutaka; Després, Viviane; Garcia, Elvin; Gochis, David; Sinha, Bärbel; Day, Douglas; Andreae, Meinrat; Jimenez, Jose; Gallagher, Martin; Kreidenweis, Sonia; Bertram, Allan; Pöschl, Ulrich

    2013-04-01

    Bioaerosols are relevant for public health and may play an important role in the climate system, but their atmospheric abundance, properties and sources are not well understood. Here we show that the concentration of airborne biological particles in a forest ecosystem increases dramatically during rain and that bioparticles are closely correlated with atmospheric ice nuclei (IN). The greatest increase of bioparticles and IN occurred in the size range of 2-6 µm, which is characteristic for bacterial aggregates and fungal spores. By DNA analysis we found high diversities of airborne bacteria and fungi, including human and plant pathogens (mildew, smut and rust fungi, molds, Enterobacteraceae, Pseudomonadaceae). In addition to known bacterial and fungal IN (Pseudomonas sp., Fusarium sporotrichioides), we discovered two species of IN-active fungi that were not previously known as biological ice nucleators (Isaria farinosa and Acremonium implicatum). Our findings suggest that atmospheric bioaerosols, IN and rainfall are more tightly coupled than previously assumed.

  2. Aerosol distributions and an Arctic aerosol front during AGASP: Norwegian Arctic

    SciTech Connect

    Raatz, W.E.; Schnell, R.C.

    1984-05-01

    Vertical profiles of aerosol characteristics obtained near Svalbard, Norway, during the Arctic Gas and Aerosol Sampling Program (AGASP) indicate that high aerosol concentrations and strong visible haze were distributed throughout the troposphere. Layers of Arctic haze were observed in both dry air and moist air. A research flight on March 31, 1983, crossed a previously undocumented Arctic aerosol front structure. Condensation nucleus concentrations of 450 cm/sup -3/ within the polluted continental air mass south of the front decreased to 80 cm/sup -3/ within the clean Arctic air north of the front. Aerosols above the Aitken size range decreased one order of magnitude in both number and mass across this same air mass boundary.

  3. Measurements of Atmospheric Aerosol Vertical Distributions above Svalbard, Norway using Unmanned Aerial Systems (UAS)

    NASA Astrophysics Data System (ADS)

    Bates, T. S.; Johnson, J. E.; Stalin, S.; Telg, H.; Murphy, D. M.; Burkhart, J. F.; Quinn, P.; Storvold, R.

    2015-12-01

    Atmospheric aerosol vertical distributions were measured above Svalbard, Norway in April 2015 to investigate the processes controlling aerosol concentrations and radiative effects. The aerosol payload was flown in a NOAA/PMEL MANTA Unmanned Aerial System (UAS) on 9 flights totaling 19 flight hours. Measurements were made of particle number concentration and aerosol light absorption at three wavelengths, similar to those conducted in April 2011 (Bates et al., Atmos. Meas. Tech., 6, 2115-2120, 2013). A filter sample was collected on each flight for analyses of trace elements. Additional measurements in the aerosol payload in 2015 included aerosol size distributions obtained using a Printed Optical Particle Spectrometer (POPS) and aerosol optical depth obtained using a four wavelength miniature Scanning Aerosol Sun Photometer (miniSASP). The data show most of the column aerosol mass and resulting optical depth in the boundary layer but frequent aerosol layers aloft with high particle number concentration (2000 cm-3) and enhanced aerosol light absorption (1 Mm-1). Transport of these aerosol layers was assessed using FLEXPART particle dispersion models. The data contribute to an assessment of sources of BC to the Arctic and potential climate impacts.

  4. Measuring effective radium concentration with large numbers of samples. Part II--general properties and representativity.

    PubMed

    Girault, Frédéric; Perrier, Frédéric

    2012-11-01

    Effective radium concentration EC(Ra), product of radium concentration and radon emanation, is the source term for radon release into the pore space of rocks and the environment. Over a period of three years, we performed more than 6000 radon-222 accumulation experiments in the laboratory with scintillation flasks and SSNTDs and we obtained experimental EC(Ra) values from more than 1570 rock and soil samples. With this method, which allowed the measurement of EC(Ra) from large numbers of samples with sufficient accuracy and uncertainty, as detailed in the companion paper, the dependence of the emanation factor on temperature and moisture content is revisited. In addition, with such a large EC(Ra) dataset, dispersion of EC(Ra) can be studied at sample-scale (cm to dm) and at scarp-scale (m to tens of m). Furthermore, we are able to discuss the representativity of obtained EC(Ra) values at field-scale, and to investigate the spatial variations of EC(Ra) over kilometric scales, within geological formations and across formations and faults. This experimental study opens new perspectives in the understanding of radium geochemistry and illustrates the importance of studying the radon source term with large numbers of samples for the modelling of geological and environmental processes, and also for the assessment of the radon health hazard.

  5. High concentrations of biological aerosol particles and ice nuclei during and after rain

    NASA Astrophysics Data System (ADS)

    Huffman, J. A.; Prenni, A. J.; DeMott, P. J.; Pöhlker, C.; Mason, R. H.; Robinson, N. H.; Fröhlich-Nowoisky, J.; Tobo, Y.; Després, V. R.; Garcia, E.; Gochis, D. J.; Harris, E.; Müller-Germann, I.; Ruzene, C.; Schmer, B.; Sinha, B.; Day, D. A.; Andreae, M. O.; Jimenez, J. L.; Gallagher, M.; Kreidenweis, S. M.; Bertram, A. K.; Pöschl, U.

    2013-07-01

    Bioaerosols are relevant for public health and may play an important role in the climate system, but their atmospheric abundance, properties, and sources are not well understood. Here we show that the concentration of airborne biological particles in a North American forest ecosystem increases significantly during rain and that bioparticles are closely correlated with atmospheric ice nuclei (IN). The greatest increase of bioparticles and IN occurred in the size range of 2-6 μm, which is characteristic for bacterial aggregates and fungal spores. By DNA analysis we found high diversities of airborne bacteria and fungi, including groups containing human and plant pathogens (mildew, smut and rust fungi, molds, Enterobacteriaceae, Pseudomonadaceae). In addition to detecting known bacterial and fungal IN (Pseudomonas sp., Fusarium sporotrichioides), we discovered two species of IN-active fungi that were not previously known as biological ice nucleators (Isaria farinosa and Acremonium implicatum). Our findings suggest that atmospheric bioaerosols, IN, and rainfall are more tightly coupled than previously assumed.

  6. 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

  7. 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.

  8. Occupational Exposure to Cobalt and Tungsten in the Swedish Hard Metal Industry: Air Concentrations of Particle Mass, Number, and Surface Area

    PubMed Central

    Bryngelsson, Ing-Liss; Pettersson, Carin; Husby, Bente; Arvidsson, Helena; Westberg, Håkan

    2016-01-01

    number. Linear regression analysis of the same data showed statistically significant regression coefficients only for the mass-based aerosol measures. Similar results were seen for rank correlation in the stationary rig, and linear regression analysis implied significant correlation for mass-based and particle surface area measures. The mass-based air concentration levels of cobalt and tungsten in the hard metal plant in our study were low compared to Swedish OELs. Particle number and particle surface area concentrations were in the same order of magnitude as for other industrial settings. Regression analysis implied the use of stationary determined mass-based and particle surface area aerosol concentration as proxies for various exposure measures in our study. PMID:27143598

  9. Occupational Exposure to Cobalt and Tungsten in the Swedish Hard Metal Industry: Air Concentrations of Particle Mass, Number, and Surface Area.

    PubMed

    Klasson, Maria; Bryngelsson, Ing-Liss; Pettersson, Carin; Husby, Bente; Arvidsson, Helena; Westberg, Håkan

    2016-07-01

    . Linear regression analysis of the same data showed statistically significant regression coefficients only for the mass-based aerosol measures. Similar results were seen for rank correlation in the stationary rig, and linear regression analysis implied significant correlation for mass-based and particle surface area measures. The mass-based air concentration levels of cobalt and tungsten in the hard metal plant in our study were low compared to Swedish OELs. Particle number and particle surface area concentrations were in the same order of magnitude as for other industrial settings. Regression analysis implied the use of stationary determined mass-based and particle surface area aerosol concentration as proxies for various exposure measures in our study.

  10. How We Can Constrain Aerosol Type Globally

    NASA Technical Reports Server (NTRS)

    Kahn, Ralph

    2016-01-01

    In addition to aerosol number concentration, aerosol size and composition are essential attributes needed to adequately represent aerosol-cloud interactions (ACI) in models. As the nature of ACI varies enormously with environmental conditions, global-scale constraints on particle properties are indicated. And although advanced satellite remote-sensing instruments can provide categorical aerosol-type classification globally, detailed particle microphysical properties are unobtainable from space with currently available or planned technologies. For the foreseeable future, only in situ measurements can constrain particle properties at the level-of-detail required for ACI, as well as to reduce uncertainties in regional-to-global-scale direct aerosol radiative forcing (DARF). The limitation of in situ measurements for this application is sampling. However, there is a simplifying factor: for a given aerosol source, in a given season, particle microphysical properties tend to be repeatable, even if the amount varies from day-to-day and year-to-year, because the physical nature of the particles is determined primarily by the regional environment. So, if the PDFs of particle properties from major aerosol sources can be adequately characterized, they can be used to add the missing microphysical detail the better sampled satellite aerosol-type maps. This calls for Systematic Aircraft Measurements to Characterize Aerosol Air Masses (SAM-CAAM). We are defining a relatively modest and readily deployable, operational aircraft payload capable of measuring key aerosol absorption, scattering, and chemical properties in situ, and a program for characterizing statistically these properties for the major aerosol air mass types, at a level-of-detail unobtainable from space. It is aimed at: (1) enhancing satellite aerosol-type retrieval products with better aerosol climatology assumptions, and (2) improving the translation between satellite-retrieved aerosol optical properties and

  11. Estimating Size-Resolved Surface Particulate Matter Concentrations Using MISR High-Resolution Size-Fractionated Aerosol Optical Depth

    NASA Astrophysics Data System (ADS)

    Franklin, M.; Kalashnikova, O. V.; Garay, M. J.

    2015-12-01

    There is significant public health interest in gaining a better understanding of the health effects associated with particulate matter (PM) of different composition and size, yet ground-based monitoring data for such PM species is extremely limited. Due to their spatial and temporal coverage, satellite observations of total column aerosol optical depth (AOD) have increasingly been used to estimate surface concentrations of PM. While techniques for using satellite observations of AOD to predict surface concentrations of PM2.5 have been established, predicting surface concentrations of different particle sizes and species is more challenging. The Multi-angle Imaging SpectroRadiometer (MISR) instrument has the unique capability of estimating both total column AOD as well as total column size fractionated (small, medium and large) AOD. Using MISR AOD and AOD size fractionated products derived from high-resolution (275 m) observations reported at a spatial scale of 4.4 km in combination with national Air Quality System (AQS) monitoring data over the 2008-2009 period, we examine the association between size-fractionated MISR AOD and surface measurements of PM at different sizes (PM2.5 and PM10) and PM2.5 species (EC, OC, SO42-, NH4+) over the greater Los Angeles area. While there was a limited sample size of speciated PM data, the strongest univariate association found was between AOD and PM2.5 SO42- (R2=0.76). Incorporating meteorological data from weather stations in the area resulted in improvements to the models associating AOD with PM2.5 and PM10 mass. We found that PM2.5 was best predicted by a spatio-temporal model of AOD that also included dew point temperature and wind speed (R2=0.61), and that PM10 was best predicted by a spatio-temporal model of large fraction AOD that also included atmospheric pressure and wind speed (R2=0.65). These flexibly specified spatio-temporal models enabled reliable predictions of surface PM2.5 and PM10 concentrations at a 4.4km

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

    SciTech Connect

    Frick, G.M.; Hoppel, W.A. )

    1993-11-01

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

  13. Numerical Computation of Mass Transport in Low Reynolds Number Flows and the Concentration Boundary Layer

    NASA Astrophysics Data System (ADS)

    Licata, Nicholas A.; Fuller, Nathaniel J.

    Understanding the physical mechanisms by which an individual cell interacts with its environment often requires detailed information about the fluid in which the cell is immersed. Mass transport between the interior of the cell and the external environment is influenced by the flow of the extracellular fluid and the molecular diffusivity. Analytical calculations of the flow field are challenging in simple geometries, and not generally available in more realistic cases with irregular domain boundaries. Motivated by these problems, we discuss the numerical solution of Stokes equation by implementing a Gauss-Seidel algorithm on a staggered computational grid. The computed velocity profile is used as input to numerically solve the advection-diffusion equation for mass transport. Special attention is paid to the case of two-dimensional flows at large Péclet number. The numerical results are compared with a perturbative analytical treatment of the concentration boundary layer.

  14. 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

  15. 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

  16. Single-particle characterization of atmospheric aerosols collected at Gosan, Korea, during the Asian Pacific Regional Aerosol Characterization Experiment field campaign using low-Z (atomic number) particle electron probe X-ray microanalysis.

    PubMed

    Geng, Hong; Cheng, Fangqin; Ro, Chul-Un

    2011-11-01

    A quantitative energy-dispersive electron probe X-ray microanalysis (ED-EPMA), namely low-Z (atomic number) particle EPMA, was used to characterize the chemical compositions of the individual aerosol particles collected at the Gosan supersite, Jeju Island, Korea, as a part of the Asian Pacific Regional Aerosol Characterization Experiment (ACE-Asia). On 4-10 April 2001 just before a severe dust storm arrived, seven sets of aerosol samples were obtained by a seven-stage May cascade impactor with a flow rate of 20 L/min. Overall 11,200 particles on stages 1-6 with cutoff diameters of 16, 8, 4, 2, 1, and 0.5 microm, respectively, were examined and classified based on their secondary electron images and X-ray spectra. In general, sea salt particles were the most frequently encountered, followed by mineral dust, organic carbon (OC)-like, (NH4)2SO4/NH4HSO4-containing, elemental carbon (EC)-like, Fe-rich, and K-rich particles. Sea salt and mineral dust particles had a higher relative abundance on stages 1-5, whereas OC-like, (NH4)2SO4/NH4HSO4-containing, Fe-rich, and K-rich particles were relatively abundant on stage 6. The analysis on relative number abundances of various particle types combined with 72-hr backward air mass trajectories indicated that a lot of reacted sea salt and reacted mineral dust (with airborne NOx and SO2 or their acidic products) and OC-like particles were carried by the air masses passing over the Yellow Sea (for sample "10 April") and many NH4HSO4/ (NH4)2SO4-containing particles were carried by the air masses passing over the Sea of Japan and Korea Strait (for samples "4-9 April"). It was concluded that the atmosphere over Jeju Island was influenced by anthropogenic SO2 and NOx, organic compounds, and secondary aerosols when Asian dust was absent.

  17. 40 CFR Table F-4 to Subpart F of... - Estimated Mass Concentration Measurement of PM2.5 for Idealized Coarse Aerosol Size Distribution

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 5 2011-07-01 2011-07-01 false Estimated Mass Concentration Measurement of PM2.5 for Idealized Coarse Aerosol Size Distribution F Table F-4 to Subpart F of Part 53... Equivalent Methods for PM2.5 Pt. 53, Subpt. F, Table F-4 Table F-4 to Subpart F of Part 53—Estimated...

  18. 40 CFR Table F-5 to Subpart F of... - Estimated Mass Concentration Measurement of PM2.5 for Idealized “Typical” Coarse Aerosol Size...

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 5 2010-07-01 2010-07-01 false Estimated Mass Concentration Measurement of PM2.5 for Idealized âTypicalâ Coarse Aerosol Size Distribution F Table F-5 to Subpart F of Part... of Class II Equivalent Methods for PM2.5 Pt. 53, Subpt. F, Table F-5 Table F-5 to Subpart F of...

  19. 40 CFR Table F-6 to Subpart F of... - Estimated Mass Concentration Measurement of PM2.5 for Idealized Fine Aerosol Size Distribution

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 5 2010-07-01 2010-07-01 false Estimated Mass Concentration Measurement of PM2.5 for Idealized Fine Aerosol Size Distribution F Table F-6 to Subpart F of Part 53... Equivalent Methods for PM2.5 Pt. 53, Subpt. F, Table F-6 Table F-6 to Subpart F of Part 53—Estimated...

  20. 40 CFR Table F-4 to Subpart F of... - Estimated Mass Concentration Measurement of PM2.5 for Idealized Coarse Aerosol Size Distribution

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 5 2010-07-01 2010-07-01 false Estimated Mass Concentration Measurement of PM2.5 for Idealized Coarse Aerosol Size Distribution F Table F-4 to Subpart F of Part 53... Equivalent Methods for PM2.5 Pt. 53, Subpt. F, Table F-4 Table F-4 to Subpart F of Part 53—Estimated...

  1. 40 CFR Table F-5 to Subpart F of... - Estimated Mass Concentration Measurement of PM2.5 for Idealized “Typical” Coarse Aerosol Size...

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 5 2011-07-01 2011-07-01 false Estimated Mass Concentration Measurement of PM2.5 for Idealized âTypicalâ Coarse Aerosol Size Distribution F Table F-5 to Subpart F of Part... of Class II Equivalent Methods for PM2.5 Pt. 53, Subpt. F, Table F-5 Table F-5 to Subpart F of...

  2. 40 CFR Table F-6 to Subpart F of... - Estimated Mass Concentration Measurement of PM2.5 for Idealized Fine Aerosol Size Distribution

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 5 2011-07-01 2011-07-01 false Estimated Mass Concentration Measurement of PM2.5 for Idealized Fine Aerosol Size Distribution F Table F-6 to Subpart F of Part 53... Equivalent Methods for PM2.5 Pt. 53, Subpt. F, Table F-6 Table F-6 to Subpart F of Part 53—Estimated...

  3. Understanding Ice Supersaturation, Particle Growth, and Number Concentration in Cirrus Clouds

    NASA Technical Reports Server (NTRS)

    Comstock, Jennifer M.; Lin, Ruei-Fong; Starr, David O'C.; Yang, Ping

    2008-01-01

    Many factors control the ice supersaturation and microphysical properties in cirrus clouds. We explore the effects of dynamic forcing, ice nucleation mechanisms, and ice crystal growth rate on the evolution and distribution of water vapor and cloud properties in nighttime cirrus clouds using a one-dimensional cloud model with bin microphysics and remote sensing measurements obtained at the Department of Energy's Atmospheric Radiation Measurement (ARM) Climate Research Facility located near Lamont, OK. We forced the model using both large-scale vertical ascent and, for the first time, mean mesoscale velocity derived from radar Doppler velocity measurements. Both heterogeneous and homogeneous nucleation processes are explored, where a classical theory heterogeneous scheme is compared with empirical representations. We evaluated model simulations by examining both bulk cloud properties and distributions of measured radar reflectivity, lidar extinction, and water vapor profiles, as well as retrieved cloud microphysical properties. Our results suggest that mesoscale variability is the primary mechanism needed to reproduce observed quantities. Model sensitivity to the ice growth rate is also investigated. The most realistic simulations as compared with observations are forced using mesoscale waves, include fast ice crystal growth, and initiate ice by either homogeneous or heterogeneous nucleation. Simulated ice crystal number concentrations (tens to hundreds particles per liter) are typically two orders of magnitude smaller than previously published results based on aircraft measurements in cirrus clouds, although higher concentrations are possible in isolated pockets within the nucleation zone.

  4. GCM Simulations of the Aerosol Indirect Effect: Sensitivity to Cloud Parameterization and Aerosol Burden

    NASA Technical Reports Server (NTRS)

    Menon, Surabi; DelGenio, Anthony D.; Koch, Dorothy; Tselioudis, George; Hansen, James E. (Technical Monitor)

    2001-01-01

    We describe the coupling of the Goddard Institute for Space Studies (GISS) general circulation model (GCM) to an online sulfur chemistry model and source models for organic matter and sea-salt that is used to estimate the aerosol indirect effect. The cloud droplet number concentration is diagnosed empirically from field experiment datasets over land and ocean that observe droplet number and all three aerosol types simultaneously; corrections are made for implied variations in cloud turbulence levels. The resulting cloud droplet number is used to calculate variations in droplet effective radius, which in turn allows us to predict aerosol effects on cloud optical thickness and microphysical process rates. We calculate the aerosol indirect effect by differencing the top-of-the-atmosphere net cloud radiative forcing for simulations with present-day vs. pre-industrial emissions. Both the first (radiative) and second (microphysical) indirect effects are explored. We test the sensitivity of our results to cloud parameterization assumptions that control the vertical distribution of cloud occurrence, the autoconversion rate, and the aerosol scavenging rate, each of which feeds back significantly on the model aerosol burden. The global mean aerosol indirect effect for all three aerosol types ranges from -1.55 to -4.36 W m(exp -2) in our simulations. The results are quite sensitive to the pre-industrial background aerosol burden, with low pre-industrial burdens giving strong indirect effects, and to a lesser extent to the anthropogenic aerosol burden, with large burdens giving somewhat larger indirect effects. Because of this dependence on the background aerosol, model diagnostics such as albedo-particle size correlations and column cloud susceptibility, for which satellite validation products are available, are not good predictors of the resulting indirect effect.

  5. GCM Simulations of the Aerosol Indirect Effect: Sensitivity to Cloud Parameterization and Aerosol Burden

    NASA Technical Reports Server (NTRS)

    Menon, Surabi; DelGenio, Anthony D.; Koch, Dorothy; Tselioudis, George; Hansen, James E. (Technical Monitor)

    2001-01-01

    We describe the coupling of the Goddard Institute for Space Studies (GISS) general circulation model (GCM) to an online sulfur chemistry model and source models for organic matter and sea-salt that is used to estimate the aerosol indirect effect. The cloud droplet number concentration is diagnosed empirically from field experiment datasets over land and ocean that observe droplet number and all three aerosol types simultaneously; corrections are made for implied variations in cloud turbulence levels. The resulting cloud droplet number is used to calculate variations in droplet effective radius, which in turn allows us to predict aerosol effects on cloud optical thickness and microphysical process rates. We calculate the aerosol indirect effect by differencing the top-of-the-atmosphere net cloud radiative forcing for simulations with