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Sample records for aerosol distribution sea

  1. Size distributions and source function of sea spray aerosol over the South China Sea

    NASA Astrophysics Data System (ADS)

    Chu, Yingjia; Sheng, Lifang; Liu, Qian; Zhao, Dongliang; Jia, Nan; Kong, Yawen

    2016-08-01

    The number concentrations in the radius range of 0.06-5 μm of aerosol particles and meteorological parameters were measured on board during a cruise in the South China Sea from August 25 to October 12, 2012. Effective fluxes in the reference height of 10 m were estimated by steady state dry deposition method based on the observed data, and the influences of different air masses on flux were discussed in this paper. The number size distribution was characterized by a bimodal mode, with the average total number concentration of (1.50 ± 0.76)×103 cm-3. The two mode radii were 0.099 µm and 0.886 µm, both of which were within the scope of accumulation mode. A typical daily average size distribution was compared with that measured in the Bay of Bengal. In the whole radius range, the number concentrations were in agreement with each other; the modes were more distinct in this study than that abtained in the Bay of Bengal. The size distribution of the fluxes was fitted with the sum of log-normal and power-law distribution. The impact of different air masses was mainly on flux magnitude, rather than the shape of spectral distribution. A semiempirical source function that is applicable in the radius range of 0.06 µm< r 80<0.3 µm with the wind speed varying from 1.00 m s-1 to 10.00 m s-1 was derived.

  2. Spatial distribution of carbonaceous aerosol in the southeastern Baltic Sea region (event of grass fires)

    NASA Astrophysics Data System (ADS)

    Dudoitis, Vadimas; Byčenkienė, Steigvilė; Plauškaitė, Kristina; Bozzetti, Carlo; Fröhlich, Roman; Mordas, Genrik; Ulevičius, Vidmantas

    2016-05-01

    The aerosol chemical composition in air masses affected by large vegetation fires transported from the Kaliningrad region (Russia) and southeast regions (Belarus and Ukraine) during early spring (March 2014) was characterized at the remote background site of Preila, Lithuania. In this study, the chemical composition of the particulate matter was studied by high temporal resolution instruments, including an Aerosol Chemical Speciation Monitor (ACSM) and a seven-wavelength aethalometer. Air masses were transported from twenty to several hundred kilometres, arriving at the measurement station after approximately half a day of transport. The concentration-weighted trajectory analysis suggests that organic aerosol particles are mainly transported over the Baltic Sea and the continent (southeast of Belarus). Results show that a significant fraction of the vegetation burning organic aerosol is transformed into oxidised forms in less than a half-day. Biomass burning aerosol (BBOA) was quantified from the ACSM data using a positive matrix factorization (PMF) analysis, while its spatial distribution was evaluated using air mass clustering approach.

  3. Massive-scale aircraft observations of giant sea-salt aerosol particle size distributions in atmospheric marine boundary layers

    NASA Astrophysics Data System (ADS)

    Jensen, J. B.

    2015-12-01

    iant sea-salt aerosol particles (dry radius, rd > 0.5 μm) occur nearly everywhere in the marine boundary layer and frequently above. This study presents observations of atmospheric sea-salt size distributions in the range 0.7 < rd < 14 μm based on external impaction of sea-spray aerosol particles onto microscope polycarbonate microscope slides. The slides have very large sample volumes, typically about 250 L over a 10-second sampling period. This provides unprecedented sampling of giant sea-salt particles for flights in marine boundary layer air. The slides were subsequently analyzed in a humidified chamber using dual optical digital microscopy. At a relative humidity of 90% the sea-salt aerosol particles form spherical cap drops. Based on measurement the volume of the spherical cap drop and assuming NaCl composition, the Kohler equation is used to derive the dry salt mass of tens of thousands of individual aerosol particles on each slide. Size distributions are given with a 0.2 μm resolution. The slides were exposed from the NSF/NCAR C-130 research aircraft during the 2008 VOCALS project off the coast of northern Chile and the 2011 ICE-T in the Caribbean. In each deployment, size distributions using hundreds of slides are used to relate fitted log-normal size distributions parameters to wind speed, altitude and other atmospheric conditions. The size distributions provide a unique observational set for initializing cloud models with coarse-mode aerosol particle observations for marine atmospheres.

  4. 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

  5. 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.

  6. Size Distribution and Chemical Characteristic of Aerosols in Northwestern Black Sea Region of Turkey

    NASA Astrophysics Data System (ADS)

    Oztürk, Fatma; Keles, Melek; Halif Ngagine, Soulemane

    2016-04-01

    Size segregated PM samples were collected at the city center of Bolu, which is northwestern part of the Black Sea region of Turkey between 2015 and 2016. A cascade impactor was used for the collection of weekly PM samples on pre-fired quartz filters in eight different size ranges (9.0-10.0 μm, 5.8-9.0 μm, 4.7-5.8 μm, 3.3-4.7 μm, 2.1-3.3 μm, 1.1-2.1 μm, 0.65-1.1 μm, 0.43-0.65 μm). The collected samples were divided in three parts and each part was analyzed with different analytical technique. The first part of the filter was analyzed in terms of major ions (SO42-, NO3-, Cl-, NH4+, K+, Ca2+, Mg2+, Na+). A large suit of metals from Li to U were determined in the second fraction of the filter by means of ICPMS. Lastly, the third part of the filter was analyzed in terms of EC and OC. The preliminary results indicated that the PM mass depicted bimodal distribution and the average concentration of PM10 was about 100 μg/m3for a five week period. Both EC and OC showed bi-modal distribution while these two parameters were more enriched on smaller particles. The average concentrations of EC and OC in PM1 were determined as 4.1 and 40.6 μg/m3, respectively, indicating the secondary organic aerosol formation in Bolu ambient air. Among the major ions, SO42- and NH4+ depicted unimodal distribution having significantly higher concentrations in fine particles (< 1 μm) while the rest of the ions present bimodal distribution. Mass closure analysis will be applied to the generated data set and sources will be evaluated by applying PMF. This project was supported financially by Turkish Scientific and Technological Research Council (TÜBİTAK) with a project number 114Y429.

  7. Distribution of trace gases and aerosols in the troposphere over West Siberia and Kara Sea

    NASA Astrophysics Data System (ADS)

    Belan, Boris D.; Arshinov, Mikhail Yu.; Paris, Jean-Daniel; Nédélec, Philippe; Ancellet, Gérard; Pelon, Jacques; Berchet, Antoine; Arzoumanian, Emmanuel; Belan, Sergey B.; Penner, Johannes E.; Balin, Yurii S.; Kokhanenko, Grigorii; Davydov, Denis K.; Ivlev, Georgii A.; Kozlov, Artem V.; Kozlov, Alexander S.; Chernov, Dmitrii G.; Fofonov, Alexader V.; Simonenkov, Denis V.; Tolmachev, Gennadii

    2015-04-01

    The Arctic is affected by climate change much stronger than other regions of the globe. Permafrost thawing can lead to additional methane release, which enhances the greenhouse effect and warming, as well as changes of Arctic tundra ecosystems. A great part of Siberian Arctic is still unexplored. Ground-based investigations are difficult to be carried out in this area due to it is an out-of-the-way place. So, in spite of the high cost, aircraft-based in-situ measurements can provide a good opportunity to fill up the gap in data on the atmospheric composition over this region. The ninth YAK-AEROSIB campaign was focused on the airborne survey of Arctic regions of West Siberia. It was performed in October 2014. During the campaign, the high-precision in-situ measurements of CO2, CH4, CO, O3, black carbon and aerososls, including aerosol lidar profiles, have been carried out in the Siberian troposphere from Novosibirsk to Kara Sea. Vertical distributions of the above atmospheric constituents will be presented. This work was supported by LIA YAK-AEROSIB, CNRS (France), the French Ministry of Foreign Affairs, CEA (France), the Branch of Geology, Geophysics and Mining Sciences of RAS (Program No. 5); State contracts of the Ministry of Education and Science of Russia No. 14.604.21.0100, (RFMTFIBBB210290) and No. 14.613.21.0013 (RFMEFI61314X0013); Interdisciplinary integration projects of the Siberian Branch of the Russian Academy of Science No. 35, No. 70 and No. 131; and Russian Foundation for Basic Research (grants No. 14-05-00526 and 14-05-00590).

  8. Aerosol distribution apparatus

    DOEpatents

    Hanson, W.D.

    An apparatus for uniformly distributing an aerosol to a plurality of filters mounted in a plenum, wherein the aerosol and air are forced through a manifold system by means of a jet pump and released into the plenum through orifices in the manifold. The apparatus allows for the simultaneous aerosol-testing of all the filters in the plenum.

  9. Aerosol Size Distribution in the marine regions

    NASA Astrophysics Data System (ADS)

    Markuszewski, Piotr; Petelski, Tomasz; Zielinski, Tymon; Pakszys, Paulina; Strzalkowska, Agata; Makuch, Przemyslaw; Kowalczyk, Jakub

    2014-05-01

    We would like to present the data obtained during the regular research cruises of the S/Y Oceania over a period of time between 2009 - 2012. The Baltic Sea is a very interesting polygon for aerosol measurements, however, also difficult due to the fact that mostly cases of a mixture of continental and marine aerosols are observed. It is possible to measure clear marine aerosol, but also advections of dust from southern Europe or even Africa. This variability of data allows to compare different conditions. The data is also compared with our measurements from the Arctic Seas, which have been made during the ARctic EXperiment (AREX). The Arctic Seas are very suitable for marine aerosol investigations since continental advections of aerosols are far less frequent than in other European sea regions. The aerosol size distribution was measured using the TSI Laser Aerosol Spectrometer model 3340 (99 channels, measurement range 0.09 μm to 7 μm), condensation particle counter (range 0.01 μm to 3 μm) and laser particle counter PMS CSASP-100-HV-SP (range 0.5 μm to 47 μm in 45 channels). Studies of marine aerosol production and transport are important for many Earth sciences such as cloud physics, atmospheric optics, environmental pollution studies and interaction between ocean and atmosphere. All equipment was placed on one of the masts of S/Y Oceania. Measurements using the laser aerosol spectrometer and condensation particle counter were made on one level (8 meters above sea level). Measurements with the laser particle counter were performed at five different levels above the sea level (8, 11, 14, 17 and 20 m). Based on aerosol size distribution the parameterizations with a Log-Normal and a Power-Law distributions were made. The aerosol source functions, characteristic for the region were also determined. Additionally, poor precision of the sea spray emission determination was confirmed while using only the aerosol concentration data. The emission of sea spray depends

  10. Modeling and evaluation of the global sea-salt aerosol distribution: sensitivity to emission schemes and resolution effects at coastal/orographic sites

    NASA Astrophysics Data System (ADS)

    Spada, M.; Jorba, O.; Pérez García-Pando, C.; Janjic, Z.; Baldasano, J. M.

    2013-12-01

    One of the major sources of uncertainty in model estimates of the global sea-salt aerosol distribution is the emission parameterization. We evaluate a new sea-salt aerosol life cycle module coupled to the online multiscale chemical transport model NMMB/BSC-CTM. We compare 5 yr global simulations using five state-of-the-art sea-salt open-ocean emission schemes with monthly averaged coarse aerosol optical depth (AOD) from selected AERONET sun photometers, surface concentration measurements from the University of Miami's Ocean Aerosol Network, and measurements from two NOAA/PMEL cruises (AEROINDOEX and ACE1). Model results are highly sensitive to the introduction of sea-surface-temperature (SST)-dependent emissions and to the accounting of spume particles production. Emission ranges from 3888 Tg yr-1 to 8114 Tg yr-1, lifetime varies between 7.3 h and 11.3 h, and the average column mass load is between 5.0 Tg and 7.2 Tg. Coarse AOD is reproduced with an overall correlation of around 0.5 and with normalized biases ranging from +8.8% to +38.8%. Surface concentration is simulated with normalized biases ranging from -9.5% to +28% and the overall correlation is around 0.5. Our results indicate that SST-dependent emission schemes improve the overall model performance in reproducing surface concentrations. On the other hand, they lead to an overestimation of the coarse AOD at tropical latitudes, although it may be affected by uncertainties in the comparison due to the use of all-sky model AOD, the treatment of water uptake, deposition and optical properties in the model and/or an inaccurate size distribution at emission.

  11. The Impact of Aerosol Particle Mixing State on the Hygroscopicity of Sea Spray Aerosol

    PubMed Central

    2015-01-01

    Aerosol particles influence global climate by determining cloud droplet number concentrations, brightness, and lifetime. Primary aerosol particles, such as those produced from breaking waves in the ocean, display large particle–particle variability in chemical composition, morphology, and physical phase state, all of which affect the ability of individual particles to accommodate water and grow into cloud droplets. Despite such diversity in molecular composition, there is a paucity of methods available to assess how particle–particle variability in chemistry translates to corresponding differences in aerosol hygroscopicity. Here, an approach has been developed that allows for characterization of the distribution of aerosol hygroscopicity within a chemically complex population of atmospheric particles. This methodology, when applied to the interpretation of nascent sea spray aerosol, provides a quantitative framework for connecting results obtained using molecular mimics generated in the laboratory with chemically complex ambient aerosol. We show that nascent sea spray aerosol, generated in situ in the Atlantic Ocean, displays a broad distribution of particle hygroscopicities, indicative of a correspondingly broad distribution of particle chemical compositions. Molecular mimics of sea spray aerosol organic material were used in the laboratory to assess the volume fractions and molecular functionality required to suppress sea spray aerosol hygroscopicity to the extent indicated by field observations. We show that proper accounting for the distribution and diversity in particle hygroscopicity and composition are important to the assessment of particle impacts on clouds and global climate. PMID:27162963

  12. The Impact of Aerosol Particle Mixing State on the Hygroscopicity of Sea Spray Aerosol.

    PubMed

    Schill, Steven R; Collins, Douglas B; Lee, Christopher; Morris, Holly S; Novak, Gordon A; Prather, Kimberly A; Quinn, Patricia K; Sultana, Camille M; Tivanski, Alexei V; Zimmermann, Kathryn; Cappa, Christopher D; Bertram, Timothy H

    2015-06-24

    Aerosol particles influence global climate by determining cloud droplet number concentrations, brightness, and lifetime. Primary aerosol particles, such as those produced from breaking waves in the ocean, display large particle-particle variability in chemical composition, morphology, and physical phase state, all of which affect the ability of individual particles to accommodate water and grow into cloud droplets. Despite such diversity in molecular composition, there is a paucity of methods available to assess how particle-particle variability in chemistry translates to corresponding differences in aerosol hygroscopicity. Here, an approach has been developed that allows for characterization of the distribution of aerosol hygroscopicity within a chemically complex population of atmospheric particles. This methodology, when applied to the interpretation of nascent sea spray aerosol, provides a quantitative framework for connecting results obtained using molecular mimics generated in the laboratory with chemically complex ambient aerosol. We show that nascent sea spray aerosol, generated in situ in the Atlantic Ocean, displays a broad distribution of particle hygroscopicities, indicative of a correspondingly broad distribution of particle chemical compositions. Molecular mimics of sea spray aerosol organic material were used in the laboratory to assess the volume fractions and molecular functionality required to suppress sea spray aerosol hygroscopicity to the extent indicated by field observations. We show that proper accounting for the distribution and diversity in particle hygroscopicity and composition are important to the assessment of particle impacts on clouds and global climate.

  13. The Impact of Aerosol Particle Mixing State on the Hygroscopicity of Sea Spray Aerosol.

    PubMed

    Schill, Steven R; Collins, Douglas B; Lee, Christopher; Morris, Holly S; Novak, Gordon A; Prather, Kimberly A; Quinn, Patricia K; Sultana, Camille M; Tivanski, Alexei V; Zimmermann, Kathryn; Cappa, Christopher D; Bertram, Timothy H

    2015-06-24

    Aerosol particles influence global climate by determining cloud droplet number concentrations, brightness, and lifetime. Primary aerosol particles, such as those produced from breaking waves in the ocean, display large particle-particle variability in chemical composition, morphology, and physical phase state, all of which affect the ability of individual particles to accommodate water and grow into cloud droplets. Despite such diversity in molecular composition, there is a paucity of methods available to assess how particle-particle variability in chemistry translates to corresponding differences in aerosol hygroscopicity. Here, an approach has been developed that allows for characterization of the distribution of aerosol hygroscopicity within a chemically complex population of atmospheric particles. This methodology, when applied to the interpretation of nascent sea spray aerosol, provides a quantitative framework for connecting results obtained using molecular mimics generated in the laboratory with chemically complex ambient aerosol. We show that nascent sea spray aerosol, generated in situ in the Atlantic Ocean, displays a broad distribution of particle hygroscopicities, indicative of a correspondingly broad distribution of particle chemical compositions. Molecular mimics of sea spray aerosol organic material were used in the laboratory to assess the volume fractions and molecular functionality required to suppress sea spray aerosol hygroscopicity to the extent indicated by field observations. We show that proper accounting for the distribution and diversity in particle hygroscopicity and composition are important to the assessment of particle impacts on clouds and global climate. PMID:27162963

  14. Vertical Distribution and Columnar Optical Properties of Springtime Biomass-Burning Aerosols over Northern Indochina during the 7-SEAS/BASELInE field campaign

    NASA Astrophysics Data System (ADS)

    Lin, N. H.; Wang, S. H.; Welton, E. J.; Holben, B. N.; Tsay, S. C.; Giles, D. M.; Stewart, S. A.; Janjai, S.; Anh, N. X.; Hsiao, T. C.; Chen, W. N.; Lin, T. H.; Buntoung, S.; Chantara, S.; Wiriya, W.

    2015-12-01

    In this study, the aerosol optical properties and vertical distributions in major biomass-burning emission area of northern Indochina were investigated using ground-based remote sensing (i.e., four Sun-sky radiometers and one lidar) during the Seven South East Asian Studies/Biomass-burning Aerosols & Stratocumulus Environment: Lifecycles & Interactions Experiment conducted during spring 2014. Despite the high spatial variability of the aerosol optical depth (AOD; which at 500 nm ranged from 0.75 to 1.37 depending on the site), the temporal variation of the daily AOD demonstrated a consistent pattern among the observed sites, suggesting the presence of widespread smoke haze over the region. Smoke particles were characterized as small (Ångström exponent at 440-870 nm of 1.72 and fine mode fraction of 0.96), strongly absorbing (single-scattering albedo at 440 nm of 0.88), mixture of black and brown carbon particles (absorption Ångström exponent at 440-870 nm of 1.5) suspended within the planetary boundary layer (PBL). Smoke plumes driven by the PBL dynamics in the mountainous region reached as high as 5 km above sea level; these plumes subsequently spread out by westerly winds over northern Vietnam, southern China, and the neighboring South China Sea. Moreover, the analysis of diurnal variability of aerosol loading and optical properties as well as vertical profile in relation to PBL development, fire intensity, and aerosol mixing showed that various sites exhibited different variability based on meteorological conditions, fuel type, site elevation, and proximity to biomass-burning sources. These local factors influence the aerosol characteristics in the region and distinguish northern Indochina smoke from other biomass-burning regions in the world.

  15. Measurements of Hygroscopicity- and Size-Resolved Sea Spray Aerosol

    NASA Astrophysics Data System (ADS)

    Phillips, B.; Dawson, K. W.; Royalty, T. M.; Reed, R. E.; Petters, M.; Meskhidze, N.

    2015-12-01

    Atmospheric aerosols play a central role in many environmental processes by influencing the Earth's radiative balance, tropospheric chemistry, clouds, biogeochemical cycles, and visibility as well as adversely impacting human health. Based on their origin, atmospheric aerosols can be defined as anthropogenic or natural. Recent studies have shown that a large fraction of uncertainty in the radiative effects of anthropogenic aerosols is related to uncertainty in natural—background—aerosols. Marine aerosols are of particular interest due to the abundance of oceans covering the Earth's surface. Despite their importance, limited information is currently available for size- and composition-resolved marine aerosol emission fluxes. Our group has designed and built an instrument for measuring the size- and hygroscopicity-resolved sea spray aerosol fluxes. The instrument was first deployed during spring 2015 at the end of the 560 m pier of the US Army Corps of Engineers' Field Research Facility in Duck, NC. Measurements include 200 nm-sized diameter growth factor (hygroscopicity) distributions, sea spray particle flux measurements, and total sub-micron sized aerosol concentration. Ancillary ocean data includes salinity, pH, sea surface temperature, dissolved oxygen content, and relative fluorescence (proxy for [Chl-a]). Hygroscopicity distribution measurements show two broad peaks, one indicative of organics and sulfates and another suggestive of sea salt. The fraction of 200 nm-sized salt particles having hygroscopicity similar to that of sea-spray aerosol contributes up to ~24% of the distribution on days with high-speed onshore winds and up to ~3% on calm days with winds blowing from the continent. However, the total concentration of sea-spray-like particles originating from offshore versus onshore winds was relatively similar. Changes in the relative contribution of sea-salt to number concentration were caused by a concomitant changes in total aerosol concentration

  16. Influence of aerosol vertical distribution on radiative budget and climate

    NASA Astrophysics Data System (ADS)

    Nabat, Pierre; Michou, Martine; Saint-Martin, David; Watson, Laura

    2016-04-01

    Aerosols interact with shortwave and longwave radiation with ensuing consequences on radiative budget and climate. Aerosols are represented in climate models either using an interactive aerosol scheme including prognostic aerosol variables, or using climatologies, such as monthly aerosol optical depth (AOD) fields. In the first case, aerosol vertical distribution can vary rapidly, at a daily or even hourly scale, following the aerosol evolution calculated by the interactive scheme. On the contrary, in the second case, a fixed aerosol vertical distribution is generally imposed by climatological profiles. The objective of this work is to study the impact of aerosol vertical distribution on aerosol radiative forcing, with ensuing effects on climate. Simulations have thus been carried out using CNRM-CM, which is a global climate model including an interactive aerosol scheme representing the five main aerosol species (desert dust, sea-salt, sulfate, black carbon and organic matter). Several multi-annual simulations covering the past recent years are compared, including either the prognostic aerosol variables, or monthly AOD fields with different aerosol vertical distributions. In the second case, AOD fields directly come from the first simulation, so that all simulations have the same integrated aerosol loads. The results show that modifying the aerosol vertical distribution has a significant impact on radiative budget, with consequences on global climate. These differences, highlighting the importance of aerosol vertical distribution in climate models, probably come from the modification of atmospheric circulation induced by changes in the heights of the different aerosols. Besides, nonlinear effects in the superposition of aerosol and clouds reinforce the impact of aerosol vertical distribution, since aerosol radiative forcing depends highly upon the presence of clouds, and upon the relative vertical position of aerosols and clouds.

  17. Modeling and evaluation of the global sea-salt aerosol distribution: sensitivity to emission schemes and resolution effects at coastal/orographic sites

    NASA Astrophysics Data System (ADS)

    Spada, M.; Jorba, O.; Perez, C.; Janjic, Z.; Baldasano, J. M.

    2013-05-01

    We investigate two of the major sources of uncertainty in the model estimation of the global distribution of sea-salt aerosol, i.e. the sensitivity to the emission parameterization and the influence of model resolution in coastal regions characterized by complex topography and/or steep orographic barriers where some observation sites are located. We evaluate a new sea-salt aerosol lifecycle module implemented within the online chemical transport model NMMB/BSC-CTM. Because of its multiscale core, the model is able to cover a wide range of scales. Global simulations using four state-of-the-art sea-salt emission schemes are evaluated against monthly-averaged aerosol optical depth (AOD) from selected AERONET Sun photometers, surface concentration measurements from the University of Miami's Ocean Aerosol Network and measurements from two NOAA/PMEL cruises (AEROINDOEX and ACE1). The model results are highly sensitive to the introduction of SST-dependent emissions and to the accounting of spume particles production. Depending on emission scheme, annual emissions range from 4312.9 Tg to 8979.7 Tg in the 2006. Sea-salt lifetime varies between 7.7 h and 12.0 h and the annual mean column mass load is between 5.9 Tg and 7.9 Tg. Observed coarse AOD monthly averages are reproduced with an overall correlation around 0.8 (a correlation of 0.6 is produced when applying the SST dependent scheme). Although monthly-averaged surface concentrations are overall in good agreement with the observations, there is a subset of coastal sites surrounded by complex topography where the global model overestimates by a factor of 2 or more. Using regional high-resolution simulations, we show that these large errors are mostly due to the global model's inability to capture local scale effects. In New Zeland, the increase in resolution produces a significant decrease of surface concentrations (up to 40%) - due to changes in the wind circulation and precipitation driven by the orographic barrier

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

    PubMed

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

    2013-01-01

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

  19. Breaker zone aerosol dynamics in the southern Baltic Sea

    SciTech Connect

    Zielinski, T.; Zielinski, A.

    1994-12-31

    This paper presents the results of lidar based investigations of aerosol concentrations and their size distributions over the breaker zones. The measurements were carried out under various weather conditions over breaker zones of the Gulf of Gdansk (1992) and from a station on the open Baltic Sea (International Experiment BAEX in 1993).

  20. Aerosol Radiative Forcing Derived From SeaWIFS - Retrieved Aerosol Optical Properties

    NASA Technical Reports Server (NTRS)

    Chou, Mong-Dah; Chan, Pui-King; Wang, Menghua; Einaudi, Franco (Technical Monitor)

    2000-01-01

    To understand climatic implications of aerosols over global oceans, the aerosol optical properties retrieved from the Sea-viewing Wide Field-of-view Sensor (SeaWiFS) are analyzed, and the effects of the aerosols on the Earth's radiation budgets (aerosol radiative forcing, ARF) are computed using a radiative transfer model. It is found that the distribution of the SeaWiFS-retrieved aerosol optical thickness is distinctively zonal. The maximum in the equatorial region coincides with the Intertropical Convergence Zone, and the maximum in the Southern Hemispheric high latitudes coincides with the region of prevailing westerlies. The minimum aerosol optical thickness is found in the subtropical high pressure regions, especially in the Southern Hemisphere. These zonal patterns clearly demonstrate the influence of atmospheric circulation on the oceanic aerosol distribution. Over global oceans, aerosols reduce the annual mean net downward solar flux by 5.4 W m-2 at the top of the atmosphere and by 6.1 W m-2 at the surface. The largest ARF is found in the tropical Atlantic, Arabian Sea, Bay of Bengal, the coastal regions of Southeast and East Asia, and the Southern Hemispheric high latitudes. During the period of the Indonesian big fires (September-December 1997), the cooling due to aerosols is greater than 15 W m-2 at the top of the atmosphere and greater than 30 W m(exp -1) at the surface in the vicinity of the maritime continents. The atmosphere receives extra solar radiation by greater than 15 W m(exp -1) over a large area. These large changes in radiative fluxes are expected to have enhanced the atmospheric stability, weakened the atmospheric circulation, and augmented the drought condition during that period. It would be very instructive to simulate the regional climatic. The model-calculated clear sky solar flux at the top of the atmosphere is compared with that derived from the Clouds and the Earth's Radiant Energy System (CERES). The net downward solar flux of

  1. Internal mixture of sea salt, silicates, and excess sulfate in marine aerosols.

    PubMed

    Andreae, M O; Charlson, R J; Bruynseels, F; Storms, H; VAN Grieken, R; Maenhaut, W

    1986-06-27

    Individual aerosol particles from the remote marine atmosphere were investigated by scanning electron microscopy and electron microprobe analysis. A large fraction of the silicate mineral component of the aerosol was found to be internally mixed with sea-salt aerosol particles. This observation explains the unexpected similarity in the size distributions of silicates and sea salt that has been observed in remote marine aerosols. Reentrainment of dust particles previously deposited onto the sea surface and collision between aerosol particles can be excluded as possible source mechanisms for these internally mixed aerosols. The internal mixing could be produced by processes within clouds, including droplet coalescence. Cloud processes may also be responsible for the observed enrichment of excess (nonsea-salt) sulfate on sea-salt particles.

  2. Eddy Covariance Measurements of the Sea-Spray Aerosol Flu

    NASA Astrophysics Data System (ADS)

    Brooks, I. M.; Norris, S. J.; Yelland, M. J.; Pascal, R. W.; Prytherch, J.

    2015-12-01

    Historically, almost all estimates of the sea-spray aerosol source flux have been inferred through various indirect methods. Direct estimates via eddy covariance have been attempted by only a handful of studies, most of which measured only the total number flux, or achieved rather coarse size segregation. Applying eddy covariance to the measurement of sea-spray fluxes is challenging: most instrumentation must be located in a laboratory space requiring long sample lines to an inlet collocated with a sonic anemometer; however, larger particles are easily lost to the walls of the sample line. Marine particle concentrations are generally low, requiring a high sample volume to achieve adequate statistics. The highly hygroscopic nature of sea salt means particles change size rapidly with fluctuations in relative humidity; this introduces an apparent bias in flux measurements if particles are sized at ambient humidity. The Compact Lightweight Aerosol Spectrometer Probe (CLASP) was developed specifically to make high rate measurements of aerosol size distributions for use in eddy covariance measurements, and the instrument and data processing and analysis techniques have been refined over the course of several projects. Here we will review some of the issues and limitations related to making eddy covariance measurements of the sea spray source flux over the open ocean, summarise some key results from the last decade, and present new results from a 3-year long ship-based measurement campaign as part of the WAGES project. Finally we will consider requirements for future progress.

  3. Model describing the dependence of aerosol microstructure on different sea bottom types

    SciTech Connect

    Zielinski, T.; Zielinski, A.

    1996-12-31

    This model describes variations of aerosol size distribution function, aerosol fluxes and their residence times as a function of two different formula for roughness length coefficient including developing roughness and fully developed roughness, diverse sea bottom types with various slopes and different weather conditions with changing wind velocity, direction and duration. This model has been verified experimentally on two types of Baltic Sea bottoms and it allows for the good estimation of aerosol dynamics in the coastal zone provided that wind conditions and the sea bottom type are known.

  4. Production flux of sea spray aerosol

    SciTech Connect

    de Leeuw, G.; Lewis, E.; Andreas, E. L.; Anguelova, M. D.; Fairall, C. W.; O’Dowd, C.; Schulz, M.; Schwartz, S. E.

    2011-05-07

    Knowledge of the size- and composition-dependent production flux of primary sea spray aerosol (SSA) particles and its dependence on environmental variables is required for modeling cloud microphysical properties and aerosol radiative influences, interpreting measurements of particulate matter in coastal areas and its relation to air quality, and evaluating rates of uptake and reactions of gases in sea spray drops. This review examines recent research pertinent to SSA production flux, which deals mainly with production of particles with r{sub 80} (equilibrium radius at 80% relative humidity) less than 1 {micro}m and as small as 0.01 {micro}m. Production of sea spray particles and its dependence on controlling factors has been investigated in laboratory studies that have examined the dependences on water temperature, salinity, and the presence of organics and in field measurements with micrometeorological techniques that use newly developed fast optical particle sizers. Extensive measurements show that water-insoluble organic matter contributes substantially to the composition of SSA particles with r{sub 80} < 0.25 {micro}m and, in locations with high biological activity, can be the dominant constituent. Order-of-magnitude variation remains in estimates of the size-dependent production flux per white area, the quantity central to formulations of the production flux based on the whitecap method. This variation indicates that the production flux may depend on quantities such as the volume flux of air bubbles to the surface that are not accounted for in current models. Variation in estimates of the whitecap fraction as a function of wind speed contributes additional, comparable uncertainty to production flux estimates.

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

    NASA Astrophysics Data System (ADS)

    Behnert, Irina; Matthias, Volker; Doerffer, Roland

    2007-05-01

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

  6. What Can We Learn From Laboratory Studies of Inorganic Sea Spray Aerosol?

    NASA Astrophysics Data System (ADS)

    Salter, M. E.; Zieger, P.; Acosta Navarro, J. C.; Grythe, H.; Kirkevag, A.; Rosati, B.; Riipinen, I.; Nilsson, E. D.

    2015-12-01

    Since 2013 we have been operating a temperature-controlled plunging-jet sea spray aerosol chamber at Stockholm University using inorganic artificial seawater. Using size-resolved measurements of the foam bubbles responsible for the aerosol production we were able to show that it is changes to these foam bubbles which drive the observed changes in aerosol production and size distribution as water temperature changes (Salter et al., 2014). Further, by combining size-resolved measurements of aerosol production as a function of water temperature with measurements of air entrainment by the plunging-jet we have developed a temperature-dependent sea spray source function for deployment in large-scale models (Salter et al., 2015). We have also studied the hygroscopicity, morphology, and chemical composition of the inorganic sea spray aerosol produced in the chamber. The sea spray aerosol generated from artificial seawater exhibited lower hygroscopic growth than both pure NaCl and output from the E-AIM aerosol thermodynamics model when all relevant inorganic ions in the sea salt were included. Results from sensitivity tests using a large-scale earth system model suggest that the lower hygroscopicity observed in our laboratory measurements has important implications for calculations of the radiative balance of the Earth. In addition, size-dependent chemical fractionation of several inorganic ions was observed relative to the artificial seawater with potentially important implications for the chemistry of the marine boundary layer. Each of these studies suggest that there is still much to be learned from rigorous experiments using inorganic seawater proxies. Salter et al., (2014), On the seawater temperature dependence of the sea spray aerosol generated by a continuous plunging jet. J. Geophys. Res. Atmos., 119, 9052-9072, doi: 10.1002/2013JD021376 Salter et al., (2015), An empirically derived inorganic sea spray source function incorporating sea surface temperature. Atmos

  7. Bimodal size distributions of various organic acids and fatty acids in the marine atmosphere: Influence of anthropogenic aerosols, Asian dusts, and sea spray off the coast of East Asia

    NASA Astrophysics Data System (ADS)

    Mochida, Michihiro; Umemoto, Nobuhiko; Kawamura, Kimitaka; Lim, Ho-Jin; Turpin, Barbara J.

    2007-08-01

    Size-segregated (11 stages) marine aerosol samples were collected off the coast of East Asia during the ACE-Asia campaign in 2001 and were analyzed for homologous series of dicarboxylic acids (C2-C12), ω-oxocarboxylic acids (C2-C4), and n-fatty acids (C16-C30), as well as organic carbon (OC), elemental carbon, and major inorganic ions. Concentrations of OC and major diacids and oxoacids in continental polluted air masses showed predominantly submicron maxima. However, during dusty haze events, supermicron maxima were observed, suggesting a size shift due to the secondary accumulation of these components on dust as well as sea salt particles. Supermicron maxima were also found for palmitic acid (C16 fatty acid) and other lower-molecular-weight fatty acids (LFAs, C16-C19) that are emitted from a microlayer of the ocean surface. In contrast, higher-molecular-weight fatty acids (HFAs, C20-C30) were mainly detected in the submicron mode, presumably due to a substantial contribution of biomass burning aerosols. This study demonstrates a high-variability in the size distributions of organic components (i.e., between submicron and supermicron modes) in the coastal regions off East Asia. Such variations in the physical properties of the marine aerosols may be important in relation to their cloud-condensation-nuclei and light extinction activities.

  8. Characterization of aerosols above the Northern Adriatic Sea: Case studies of offshore and onshore wind conditions

    NASA Astrophysics Data System (ADS)

    Piazzola, J.; Mihalopoulos, N.; Canepa, E.; Tedeschi, G.; Prati, P.; Zarmpas, P.; Bastianini, M.; Missamou, T.; Cavaleri, L.

    2016-05-01

    Aerosol particles in coastal areas result from a complex mixing between sea spray aerosols locally generated at the sea surface by the wind-waves interaction processes and a continental component resulting from natural and/or anthropogenic sources. This paper presents a physical and chemical analysis of the aerosol data acquired from May to September 2014 in the Adriatic Sea. Aerosol distributions were measured on the Acqua Alta platform located 15 km off the coast of Venice using two Particle Measuring System probes and a chemical characterization was made using an Ion Chromatography analysis (IC). Our aim is to study both the sea-spray contribution and the anthropogenic influence in the coastal aerosol of this Mediterranean region. To this end, we focus on a comparison between the present data and the aerosol size distributions measured south of the French Mediterranean coast. For air masses of marine origin transported by southern winds on the French coast and by the Sirocco in the Adriatic, we note a good agreement between the concentrations of super-micrometer aerosols measured in the two locations. This indicates a similar sea surface production of sea-spray aerosols formed by bubble bursting processes in the two locations. In contrast, the results show larger concentrations of submicron particles in the North-Western Mediterranean compared to the Adriatic, which result probably from a larger anthropogenic background for marine conditions. In contrast, for a coastal influence, the chemical analysis presented in the present paper seems to indicate a larger importance of the anthropogenic impact in the Northern Adriatic compared to the North-Western Mediterranean.

  9. Assessment of aerosol optical property and radiative effect for the layer decoupling cases over the northern South China Sea during the 7-SEAS/Dongsha Experiment

    NASA Astrophysics Data System (ADS)

    Pani, Shantanu Kumar; Wang, Sheng-Hsiang; Lin, Neng-Huei; Tsay, Si-Chee; Lolli, Simone; Chuang, Ming-Tung; Lee, Chung-Te; Chantara, Somporn; Yu, Jin-Yi

    2016-05-01

    The aerosol radiative effect can be modulated by the vertical distribution and optical properties of aerosols, particularly when aerosol layers are decoupled. Direct aerosol radiative effects over the northern South China Sea (SCS) were assessed by incorporating an observed data set of aerosol optical properties obtained from the Seven South East Asian Studies (7-SEAS)/Dongsha Experiment into a radiative transfer model. Aerosol optical properties for a two-layer structure of aerosol transport were estimated. In the radiative transfer calculations, aerosol variability (i.e., diversity of source region, aerosol type, and vertical distribution) for the complex aerosol environment was also carefully quantified. The column-integrated aerosol optical depth (AOD) at 500 nm was 0.1-0.3 for near-surface aerosols and increased 1-5 times in presence of upper layer biomass-burning aerosols. A case study showed the strong aerosol absorption (single-scattering albedo (ω) ≈ 0.92 at 440 nm wavelength) exhibited by the upper layer when associated with predominantly biomass-burning aerosols, and the ω (≈0.95) of near-surface aerosols was greater than that of the upper layer aerosols because of the presence of mixed type aerosols. The presence of upper level aerosol transport could enhance the radiative efficiency at the surface (i.e., cooling) and lower atmosphere (i.e., heating) by up to -13.7 and +9.6 W m-2 per AOD, respectively. Such enhancement could potentially modify atmospheric stability, can influence atmospheric circulation, as well as the hydrological cycle over the tropical and low-latitude marginal northern SCS.

  10. Connecting Aerosol Size Distributions at Three Arctic Stations

    NASA Astrophysics Data System (ADS)

    Freud, E.; Krejci, R.; Tunved, P.; Barrie, L. A.

    2015-12-01

    Aerosols play an important role in Earth's energy balance mainly through interactions with solar radiation and cloud processes. There is a distinct annual cycle of arctic aerosols, with greatest mass concentrations in the spring and lowest in summer due to effective wet removal processes - allowing for new particles formation events to take place. Little is known about the spatial extent of these events as no previous studies have directly compared and linked aerosol measurements from different arctic stations during the same times. Although the arctic stations are hardly affected by local pollution, it is normally assumed that their aerosol measurements are indicative of a rather large area. It is, however, not clear if that assumption holds all the time, and how large may that area be. In this study, three different datasets of aerosol size distributions from Mt. Zeppelin in Svalbard, Station Nord in northern Greenland and Alert in the Canadian arctic, are analyzed for the measurement period of 2012-2013. All stations are 500 to 1000 km from each other, and the travel time from one station to the other is typically between 2 to 5 days. The meteorological parameters along the calculated trajectories are analyzed in order to estimate their role in the modification of the aerosol size distribution while the air is traveling from one field station to another. In addition, the exposure of the sampled air to open waters vs. frozen sea is assessed, due to the different fluxes of heat, moisture, gases and particles, that are expected to affect the aerosol size distribution. The results show that the general characteristics of the aerosol size distributions and their annual variation are not very different in all three stations, with Alert and Station Nord being more similar. This is more pronounced when looking into the cases for which the trajectory calculations indicated that the air traveled from one of the latter stations to the other. The probable causes for the

  11. The Angstrom Exponent and Bimodal Aerosol Size Distributions

    NASA Technical Reports Server (NTRS)

    Schuster, Gregory L.; Dubovik, Oleg; Holben, Brent H.

    2005-01-01

    Powerlaws have long been used to describe the spectral dependence of aerosol extinction, and the wavelength exponent of the aerosol extinction powerlaw is commonly referred to as the Angstrom exponent. The Angstrom exponent is often used as a qualitative indicator of aerosol particle size, with values greater than two indicating small particles associated with combustion byproducts, and values less than one indicating large particles like sea salt and dust. In this study, we investigate the relationship between the Angstrom exponent and the mode parameters of bimodal aerosol size distributions using Mie theory calculations and Aerosol Robotic Network (AERONET) retrievals. We find that Angstrom exponents based upon seven wavelengths (0.34, 0.38, 0.44, 0.5, 0.67, 0.87, and 1.02 micrometers) are sensitive to the volume fraction of aerosols with radii less then 0.6 micrometers, but not to the fine mode effective radius. The Angstrom exponent is also known to vary with wavelength, which is commonly referred to as curvature; we show how the spectral curvature can provide additional information about aerosol size distributions for intermediate values of the Angstrom exponent. Curvature also has a significant effect on the conclusions that can be drawn about two-wavelength Angstrom exponents; long wavelengths (0.67, 0.87 micrometers) are sensitive to fine mode volume fraction of aerosols but not fine mode effective radius, while short wavelengths (0.38, 0.44 micrometers) are sensitive to the fine mode effective radius but not the fine mode volume fraction.

  12. The effects of mineral aerosol deposits on the BRDF (bidirectional reflectance distribution function) of sea ice for the calibration of satellite remote sensing products: an experimental and modelling study.

    NASA Astrophysics Data System (ADS)

    Lamare, Maxim; Hedley, John; King, Martin

    2016-04-01

    Knowledge of the albedo in the cryosphere is essential to monitor a range of climatic processes that have an impact on a global scale. Optical Earth Observation satellites are ideal for the synoptic observation of expansive and inaccessible areas, providing large datasets used to derive essential products, such as albedo. The application of remote sensing to investigate climate processes requires the combination of data from different sensors. However, although there is significant value in the analysis of data from individual sensors, global observing systems require accurate knowledge of sensor-to-sensor biases. Therefore, the inter-calibration of sensors used for climate studies is essential to avoid inconsistencies, which may mask climate effects. CEOS (Committee on Earth Observing Satellites) has established a number of natural Earth targets to serve as international reference standards, amongst which sea ice has great potential. The reflectance of natural surfaces is not isotropic and reflectance varies with the illumination and viewing geometries, consequently impacting satellite observations. Furthermore, variations in the physical properties (sea ice type, thickness) and the light absorbing impurities deposited in the sea ice have a strong impact on reflectance. Thus, the characterisation of the bi-directional reflectance distribution function (BRDF) of sea ice is a fundamental step toward the inter-calibration of optical satellite sensors. This study provides a characterisation of the effects of mineral aerosol and black carbon deposits on the BRDF of three different sea ice types. BRDF measurements were performed on bare sea ice grown in an experimental ice tank, using a state-of-the-art laboratory goniometer. The sea ice was "poisoned" with concentrations of mineral dust and black carbon varying between 100 and 5 000 ng g-1 deposited uniformly in a 5 cm surface layer. Using measurements from the experimental facility, novel information about sea ice

  13. 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.

  14. The contribution of anthropogenic sources to the aerosols over East China Sea

    NASA Astrophysics Data System (ADS)

    Wang, Fujiang; Chen, Ying; Meng, Xi; Fu, Jiangping; Wang, Bo

    2016-02-01

    Total suspended particulate (TSP) samples were collected at a pristine island (Huaniao) in northern East China Sea (ECS) between Mar. 2011 and Jan. 2013 and analyzed for the concentrations of major ions and trace elements. Aerosol sources and the distribution of source regions are identified using positive matrix factorization (PMF) and potential source contribution function (PSCF) methods. It is found that aerosols over Huaniao Island are contributed by six main factors including primary industrial emissions (11.3%), secondary aerosol (22%), oxalate-associated aerosol (15.7%), sea salt (36.7%), ship emission (6.3%) and mineral dust (8.1%). Anthropogenic source contribution to the resolved aerosol mass reached the highest (76.6%) and lowest (18%) values in January 2013 and August 2012 respectively, strongly influenced by the prevailing winds of East Asian monsoon. The main source regions of secondary aerosol are southeastern Hebei and Shandong, which is consistent with the most intensive distribution of coal-fired power plants and the largest emission of precursors in this area. Oxalate-associated aerosol is produced primarily along the coastal line. Primary industrial emissions mainly originate from southwestern Shandong and Yangtze River Delta.

  15. 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

  16. Modeling sea-salt aerosols in the atmosphere: 1. Model development

    NASA Astrophysics Data System (ADS)

    Gong, S. L.; Barrie, L. A.; Blanchet, J.-P.

    1997-02-01

    A simulation of the processes of sea-salt aerosol generation, diffusive transport, transformation, and removal as a function of particle size is incorporated into a one-dimensional version of the Canadian general climate model (GCMII). This model was then run in the North Atlantic between Iceland and Ireland during the period of January-March. Model predictions are compared to observations of sea-salt aerosols selected from a review of available studies that were subjected to strict screening criteria to ensure their representativeness. The number and mass size distribution and the wind dependency of total sea-salt aerosol mass concentrations predicted by the model compare well with observations. The modeled dependence of sea-salt aerosol concentration in the surface layer (χ, μg m-3) on 10-m wind speed (U10, m s-1) is given by?. Simulations show that both a and b change with location. The value a and b range from 0.20 and 3.1 for Mace Head, Ireland to 0.26, and 1.4 for Heimaey, Iceland. The dependence of χ on surface wind speed is weaker for smaller particles and for particles at higher altitudes. The residence time of sea-salt aerosols in the first atmospheric layer (0-166 m) ranges from 30 min for large particles (r=4-8 μm) to ˜60 hours for small particles (r=0.13-0.25 μm). Although some refinements are required for the model, it forms the basis for comparing the simulations with long-term atmospheric sea-salt measurements made at marine baseline observatories around the world and for a more comprehensive three-dimensional modeling of atmospheric sea-salt aerosols.

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

    NASA Astrophysics Data System (ADS)

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

    2013-05-01

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

  18. The role of sulfate aerosol in the formation of cloudiness over the sea

    NASA Astrophysics Data System (ADS)

    Aloyan, A. E.; Yermakov, A. N.; Arutyunyan, V. O.

    2016-07-01

    We estimate the impact of sulfate aerosols on cloudiness formation over the sea in the middle troposphere and the involvement of these particles in the formation of polar stratospheric clouds (PSCs) in the lower stratosphere. The first of these problems is solved using a combined model of moist convection and the formation of cloudiness and sulfate aerosols in the troposphere and lower stratosphere over the sea, incorporating natural emissions of sulfur-containing compounds. We have found that a significant source of condensation nuclei in the troposphere is the photochemical transformation of biogenic dimethyl sulfide (in addition to NaCl). The results of numerical experiments indicate that the absence of sulfate aerosols hinders the cloudiness formation over the sea in the middle and upper troposphere. The problem of sulfate aerosol involvement in the formation of supercooled ternary solutions (STSs) (PSC Type Ib) in the lower stratosphere is solved using a mathematical model of global transport of multicomponent gas pollutants and aerosols in the atmosphere. Using the combined model, numerical experiments were performed for the winter season in both hemispheres. Sulfate aerosols were found to really participate in the formation of STS particles. Without their participation, the formation of STS particles in the lower stratosphere would be hindered. We present the results of numerical calculations and discuss the distribution of concentrations of gaseous nitric and sulfuric acids, as well as mass concentrations of these components in STS particles.

  19. Analytic modeling of aerosol size distributions

    NASA Technical Reports Server (NTRS)

    Deepack, A.; Box, G. P.

    1979-01-01

    Mathematical functions commonly used for representing aerosol size distributions are studied parametrically. Methods for obtaining best fit estimates of the parameters are described. A catalog of graphical plots depicting the parametric behavior of the functions is presented along with procedures for obtaining analytical representations of size distribution data by visual matching of the data with one of the plots. Examples of fitting the same data with equal accuracy by more than one analytic model are also given.

  20. Trends in aerosol abundances and distributions

    NASA Technical Reports Server (NTRS)

    Turco, R. P.; Mccormick, M. P.; Clancy, R. T.; Curran, R.; Deluisi, J.; Hamill, P.; Kent, G.; Rosen, J. M.; Toon, O. B.; Yue, G.

    1989-01-01

    The properties of aerosols that reside in the upper atmosphere are described. Special emphasis is given to the influence these aerosols have on ozone observation systems, mainly through radiative effects, and on ambient ozone concentrations, mainly through chemical effects. It has long been appreciated that stratospheric particles can interfere with the remote sensing of ozone distribution. The mechanism and magnitude of this interference are evaluated. Separate sections deal with the optical properties of upper atmospheric aerosols, long-term trends in stratospheric aerosols, perturbations of the stratospheric aerosol layer by volcanic eruptions, and estimates of the impacts that such particles have on remotely measured ozone concentrations. Another section is devoted to a discussion of the polar stratospheric clouds (PSC's). These unique clouds, recently discovered by satellite observation, are now thought to be intimately connected with the Antarctic ozone hole. Accordingly, interest in PSC's has grown considerably in recent years. This chapter describes what we know about the morphology, physical chemistry, and microphysics of PSC's.

  1. SAGE II aerosol data validation based on retrieved aerosol model size distribution from SAGE II aerosol measurements

    NASA Technical Reports Server (NTRS)

    Wang, Pi-Huan; Mccormick, M. P.; Mcmaster, L. R.; Chu, W. P.; Swissler, T. J.; Osborn, M. T.; Russell, P. B.; Oberbeck, V. R.; Livingston, J.; Rosen, J. M.

    1989-01-01

    Consideration is given to aerosol correlative measurements experiments for the Stratospheric Aerosol and Gas Experiment (SAGE) II, conducted between November 1984 and July 1986. The correlative measurements were taken with an impactor/laser probe, a dustsonde, and an airborne 36-cm lidar system. The primary aerosol quantities measured by the ground-based instruments are compared with those calculated from the aerosol size distributions from SAGE II aerosol extinction measurements. Good agreement is found between the two sets of measurements.

  2. Evidence for a Significant Source of Sea Salt Aerosol from Blowing Snow Above Sea Ice in the Southern Ocean

    NASA Astrophysics Data System (ADS)

    Frey, M. M.; Brooks, I. M.; Anderson, P. A.; Nishimura, K.; Yang, X.; Jones, A. E.; Wolff, E. W.

    2014-12-01

    Over most of the Earth, sea salt aerosol (SSA) derives from sea spray and bubble bursting at the open ocean surface. SSA as the major component of marine aerosol contributes directly to the radiative balance and can act as cloud condensation nuclei. SSA can also significantly impact the lifetime of methane, ozone or mercury through the photochemical release of reactive halogens. A recent model study suggested that the sublimation of saline blowing snow above sea ice can generate more SSA than is produced from a similar area of open ocean. A winter cruise through the Weddell Sea during June - August 2013 provided unique access to a potential SSA source region in the Antarctic sea ice zone to test this hypothesis.Reported are first measurements of snow particle as well as aerosol concentrations, size distributions and chemical composition, during blowing snow events above sea ice. Snow particle spectra are found to be similar to those observed on the continent. Even though the salinity of surface and blowing snow was very low (<0.1 psu) a significant increase of aerosol in the SSA size range was observed during and after blowing snow events. This is consistent with model runs including a blowing snow parameterisation which suggest low sensitivity of SSA number densities to snow salinity within the observed range. First estimates of SSA flux from blowing snow using eddy correlation are significant, although falling below published values of the sea spray source function. We discuss the dependance of observed SSA production rates on ambient conditions as well as the significance to the Southern Ocean environment.

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

    NASA Technical Reports Server (NTRS)

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

    1999-01-01

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

  4. Copper aerosols inhibit phytoplankton growth in the Mediterranean Sea

    PubMed Central

    Jordi, Antoni; Basterretxea, Gotzon; Tovar-Sánchez, Antonio; Alastuey, Andrés; Querol, Xavier

    2012-01-01

    Aerosol deposition plays an important role in climate and biogeochemical cycles by supplying nutrients to the open ocean, in turn stimulating ocean productivity and carbon sequestration. Aerosol particles also contain elements such as copper (Cu) that are essential in trace amounts for phytoplankton physiology but that can be toxic at high concentrations. Although the toxicity of Cu associated with aerosols has been demonstrated in bioassay experiments, extrapolation of these laboratory results to natural conditions is not straightforward. This study provides observational evidence of the negative effect of aerosols containing high Cu concentrations on marine phytoplankton over a vast region of the western Mediterranean Sea. Direct aerosol measurements were combined with satellite observations, resulting in the detection of significant declines in phytoplankton biomass after atmospheric aerosol events characterized by high Cu concentrations. The declines were more evident during summer, when nanoflagellates predominate in the phytoplankton population and stratification and oligotrophic conditions prevail in the study region. Together with previous findings concerning atmospheric Cu deposition, these results demonstrate that the toxicity of Cu-rich aerosols can involve large areas of the world’s oceans. Moreover, they highlight the present vulnerability of oceanic ecosystems to Cu-rich aerosols of anthropogenic origins. Because anthropogenic emissions are increasing, large-scale negative effects on marine ecosystems can be anticipated. PMID:23236141

  5. Characterizing the Hygroscopicity of Nascent Sea Spray Aerosol from Synthetic Blooms

    NASA Astrophysics Data System (ADS)

    Forestieri, S.; Cappa, C. D.; Sultana, C. M.; Lee, C.; Wang, X.; Helgestad, T.; Moore, K.; Prather, K. A.; Cornwell, G.; Novak, G.; Bertram, T. H.

    2015-12-01

    Marine sea spray aerosol (SSA) particles make up a significant portion of natural aerosols and are therefore important in establishing the baseline for anthropogenic aerosol climate impacts. Scattering of solar radiation by aerosols affects Earth's radiative budget and the degree of scattering is size-dependent. Thus, aerosols scatter more light at elevated relative humidities when they grow larger via water uptake. This growth depends critically on chemical composition. SSA can become enriched in organics during phytoplankton blooms, becoming less salty and therefore less hygroscopic. Subsaturated hygroscopic growth factors at 85% relative humidity (GF(85%)) of SSA particles were quantified during two mesocosm experiments in enclosed marine aerosol reference tanks (MARTs). The two experiments were conducted with filtered seawater collected at separate times from the Scripps Institute of Oceanography Pier in La Jolla, CA. Phytoplankton blooms in each tank were induced via the addition of nutrients and photosynthetically active radiation. The "indoor" MART was illuminated with fluorescent light and the other "outdoor" MART was illuminated with sunlight. The peak chlorophyll-a concentrations were 59 micrograms/L and 341 micrograms /L for the indoor and outdoor MARTs, respectively. GF(85%) values for SSA particles were quantified using a humidified cavity ringdown spectrometer and particle size distributions. Particle composition was monitored with a single particle aerosol mass spectrometer (ATOFMS) and an Aerodyne aerosol mass spectrometer (AMS). Relationships between the observed particle GFs and the particle composition markers will be discussed.

  6. Size distributions of submicrometer aerosols from cooking

    SciTech Connect

    Li, C.S.; Lin, W.H.; Jeng, F.T. )

    1993-01-01

    Although gas stove usage varies from country to country, it is still one of the major indoor combustion sources. In order to assess the health effects of using gas stoves, the physical characteristics of the particle emissions from cooking were conducted in a first-floor apartment in the Taipei area. The particle size distributions from scrambling eggs, frying chicken, and cooking soup were measured in the kitchen by a high resolution particle sizer, which could measure the particles in the size range of 0.01 [mu]m to 1 [mu]m. The concentrations of the submicrometer particles increased significantly from 15,000 cm[sup [minus]3] to 150,000 cm[sup [minus]3] during cooking. Additionally, the ultrafine particles constituted 60%--70% of the total submicron aerosols. The changes in the size distributions and the concentrations of the submicrometer aerosols before, during, and after the aerosol generations were compared. On the average, the median diameters of scrambling eggs, frying chicken, cooking soup, and of the background conditions were 40 nm, 50 nm, 30 nm, and 70 nm, respectively. Regarding the surface area-weighted size distributions, the surface median diameters of the four situations were 180 nm, 300 nm, 150 nm, and 220 nm, respectively. Furthermore, the volume median diameters in the conditions mentioned above were almost similar, namely 300--350 nm. 10 refs., 6 figs., 2 tabs.

  7. The impact of atmospheric mineral aerosol deposition on the albedo of snow & sea ice: are snow and sea ice optical properties more important than mineral aerosol optical properties?

    NASA Astrophysics Data System (ADS)

    Lamare, M. L.; Lee-Taylor, J.; King, M. D.

    2016-01-01

    Knowledge of the albedo of polar regions is crucial for understanding a range of climatic processes that have an impact on a global scale. Light-absorbing impurities in atmospheric aerosols deposited on snow and sea ice by aeolian transport absorb solar radiation, reducing albedo. Here, the effects of five mineral aerosol deposits reducing the albedo of polar snow and sea ice are considered. Calculations employing a coupled atmospheric and snow/sea ice radiative-transfer model (TUV-snow) show that the effects of mineral aerosol deposits are strongly dependent on the snow or sea ice type rather than the differences between the aerosol optical characteristics. The change in albedo between five different mineral aerosol deposits with refractive indices varying by a factor of 2 reaches a maximum of 0.0788, whereas the difference between cold polar snow and melting sea ice is 0.8893 for the same mineral loading. Surprisingly, the thickness of a surface layer of snow or sea ice loaded with the same mass ratio of mineral dust has little effect on albedo. On the contrary, the surface albedo of two snowpacks of equal depth, containing the same mineral aerosol mass ratio, is similar, whether the loading is uniformly distributed or concentrated in multiple layers, regardless of their position or spacing. The impact of mineral aerosol deposits is much larger on melting sea ice than on other types of snow and sea ice. Therefore, the higher input of shortwave radiation during the summer melt cycle associated with melting sea ice accelerates the melt process.

  8. Measurements of regional-scale aerosol impacts on cloud microphysics over the East China Sea: Possible influences of warm sea surface temperature over the Kuroshio ocean current

    NASA Astrophysics Data System (ADS)

    Koike, M.; Takegawa, N.; Moteki, N.; Kondo, Y.; Nakamura, H.; Kita, K.; Matsui, H.; Oshima, N.; Kajino, M.; Nakajima, T. Y.

    2012-09-01

    Cloud microphysical properties and aerosol concentrations were measured aboard an aircraft over the East China Sea and Yellow Sea in April 2009 during the Aerosol Radiative Forcing in East Asia (A-FORCE) experiment. We sampled stratocumulus and shallow cumulus clouds over the ocean in 9 cases during 7 flights 500-900 km off the east coast of Mainland China. In this study we report aerosol impacts on cloud microphysical properties by focusing on regional characteristics of two key parameters, namely updraft velocity and aerosol size distribution. First, we show that the cloud droplet number concentration (highest 5%, Nc_max) correlates well with the accumulation-mode aerosol number concentration (Na) below the clouds. We then show that Nc_maxcorrelates partly with near-surface stratification evaluated as the difference between the sea surface temperature (SST) and 950-hPa temperature (SST - T950). Cold air advection from China to the East China Sea was found to bring not only a large number of aerosols but also a dry and cold air mass that destabilized the atmospheric boundary layer, especially over the warm Kuroshio ocean current. Over this high-SST region, greater updraft velocities and hence greater Nc_maxlikely resulted. We hypothesize that the low-level static stability determined by SST and regional-scale airflow modulates both the cloud microphysics (aerosol impact on clouds) and macro-structure of clouds (cloud base and top altitudes, hence cloud liquid water path). Second, we show that not only higher aerosol loading in terms of total aerosol number concentration (NCN, D > 10 nm) but also larger aerosol mode diameters likely contributed to high Ncduring A-FORCE. The mean Nc of 650 ± 240 cm-3was more than a factor of 2 larger than the global average for clouds influenced by continental sources. A crude estimate of the aerosol-induced cloud albedo radiative forcing is also given.

  9. Sources and characteristics of fine particles over the Yellow Sea and Bohai Sea using online single particle aerosol mass spectrometer.

    PubMed

    Fu, Huaiyu; Zheng, Mei; Yan, Caiqing; Li, Xiaoying; Gao, Huiwang; Yao, Xiaohong; Guo, Zhigang; Zhang, Yuanhang

    2015-03-01

    Marine aerosols over the East China Seas are heavily polluted by continental sources. During the Chinese Comprehensive Ocean Experiment in November 2012, size and mass spectra of individual atmospheric particles in the size range from 0.2 to 2.0 μm were measured on board by a single particle aerosol mass spectrometer (SPAMS). The average hourly particle number (PN) was around 4560±3240 in the South Yellow Sea (SYS), 2900±3970 in the North Yellow Sea (NYS), and 1700±2220 in the Bohai Sea (BS). PN in NYS and BS varied greatly over 3 orders of magnitude, while that in SYS varied slightly. The size distributions were fitted with two log-normal modes. Accumulation mode dominated in NYS and BS, especially during episodic periods. Coarse mode particles played an important role in SYS. Particles were classified using an adaptive resonance theory based neural network algorithm (ART-2a). Six particle types were identified with secondary-containing, aged sea-salt, soot-like, biomass burning, fresh sea-salt, and lead-containing particles accounting for 32%, 21%, 18%, 16%, 4%, and 3% of total PN, respectively. Aerosols in BS were relatively enriched in particles from anthropogenic sources compared to SYS, probably due to emissions from more developed upwind regions and indicating stronger influence of continental outflow on marine environment. Variation of source types depended mainly on origins of transported air masses. This study examined rapid changes in PN, size distribution and source types of fine particles in marine atmospheres. It also demonstrated the effectiveness of high-time-resolution source apportionment by ART-2a.

  10. Sources and characteristics of fine particles over the Yellow Sea and Bohai Sea using online single particle aerosol mass spectrometer.

    PubMed

    Fu, Huaiyu; Zheng, Mei; Yan, Caiqing; Li, Xiaoying; Gao, Huiwang; Yao, Xiaohong; Guo, Zhigang; Zhang, Yuanhang

    2015-03-01

    Marine aerosols over the East China Seas are heavily polluted by continental sources. During the Chinese Comprehensive Ocean Experiment in November 2012, size and mass spectra of individual atmospheric particles in the size range from 0.2 to 2.0 μm were measured on board by a single particle aerosol mass spectrometer (SPAMS). The average hourly particle number (PN) was around 4560±3240 in the South Yellow Sea (SYS), 2900±3970 in the North Yellow Sea (NYS), and 1700±2220 in the Bohai Sea (BS). PN in NYS and BS varied greatly over 3 orders of magnitude, while that in SYS varied slightly. The size distributions were fitted with two log-normal modes. Accumulation mode dominated in NYS and BS, especially during episodic periods. Coarse mode particles played an important role in SYS. Particles were classified using an adaptive resonance theory based neural network algorithm (ART-2a). Six particle types were identified with secondary-containing, aged sea-salt, soot-like, biomass burning, fresh sea-salt, and lead-containing particles accounting for 32%, 21%, 18%, 16%, 4%, and 3% of total PN, respectively. Aerosols in BS were relatively enriched in particles from anthropogenic sources compared to SYS, probably due to emissions from more developed upwind regions and indicating stronger influence of continental outflow on marine environment. Variation of source types depended mainly on origins of transported air masses. This study examined rapid changes in PN, size distribution and source types of fine particles in marine atmospheres. It also demonstrated the effectiveness of high-time-resolution source apportionment by ART-2a. PMID:25766014

  11. A Model for the Transport of Sea-Spray Aerosols in the Coastal Zone

    NASA Astrophysics Data System (ADS)

    Piazzola, J.; Tedeschi, G.; Demoisson, A.

    2015-05-01

    We study the dynamics of sea-spray particles in the coastal region of La Reunion Island on the basis of numerical simulations using the transport aerosol model MACMod (Marine Aerosol Concentration Model) and a survey of the aerosol size distributions measured at four locations at two different heights in the north-west part of the island. This allows evaluation of the performance of our model in case of pure marine air masses with implementation of accurate boundary conditions. First of all, an estimate of the aerosol concentration at 10-m height at the upwind boundary of the calculation domain is obtained using a revisited version of the MEDEX (Mediterranean Extinction) model. Estimates of the vertical profile of aerosol concentrations are then provided using aerosol data obtained at two different heights at the upwind boundary of the calculation domain. A parametrization of the vertical profiles of aerosol concentrations for maritime environment is proposed. The results are then compared to the vertical profiles of 0.532 m aerosol particle extinction coefficient obtained from lidar data provided by the Cloud-Aerosol LIdar with Orthogonal Polarization (CALIOP) and also to the data provided by the Aerosol Robotic Network (AERONET). This allows validation of the complete vertical profiles in the mixed layer and shows the validity of satellite data for determination of the vertical profiles. Two kinds of simulation were made: one without a particle advection flux at the upwind boundary of the numerical domain, whereas the second simulation was made with a particle advection flux. In the first case, the influence of the distance to the shoreline on the local sea-spray dynamics is investigated. In the second set of simulation, the particles issued from the local production in the surf zone near the shoreline are mixed with aerosols advected from the remote ocean. A good agreement between the model calculations using our boundary conditions and the data was found. The

  12. On measurements of aerosol-gas composition of the atmosphere during two expeditions in 2013 along the Northern Sea Route

    NASA Astrophysics Data System (ADS)

    Sakerin, S. M.; Bobrikov, A. A.; Bukin, O. A.; Golobokova, L. P.; Pol'kin, Vas. V.; Pol'kin, Vik. V.; Shmirko, K. A.; Kabanov, D. M.; Khodzher, T. V.; Onischuk, N. A.; Pavlov, A. N.; Potemkin, V. L.; Radionov, V. F.

    2015-11-01

    We presented the results of expedition measurements of the set of physical-chemical characteristics of atmospheric aerosol in areas of the Arctic and Far East seas, performed onboard RV Akademik Fedorov (17 August-22 September 2013) and RV Professor Khljustin (24 July-7 September 2013). The specific features of spatial distribution and time variations of aerosol optical depth (AOD) of the atmosphere in the wavelength range of 0.34-2.14 μm and boundary layer height, aerosol and black carbon mass concentrations, and disperse and chemical composition of aerosol are discussed. Over the Arctic Ocean (on the route of RV Akademik Fedorov) there is a decrease in aerosol and black carbon concentrations in a northeastern direction: higher values were observed in the region of Spitsbergen and near the Kola Peninsula; and minimum values were observed at northern margins of the Laptev Sea. Average AOD (0.5 μm) values in this remote region were 0.03; the aerosol and black carbon mass concentrations were 875 and 22 ng m-3, respectively. The spatial distributions of most aerosol characteristics over Far East seas show their latitudinal decrease in the northern direction. On transit of RV Professor Khljustin from the Japan Sea to the Chukchi Sea, the aerosol number concentration decreased on average from 23.7 to 2.5 cm-3, the black carbon mass concentration decreased from 150 to 50 ng m-3, and AOD decreased from 0.19 to 0.03. We analyzed the variations in the boundary layer height, measured by ship-based lidar: the average value was 520 m, and the maximal value was 1200 m. In latitudinal distribution of the boundary layer height, there is a characteristic minimum at a latitude of ~ 55° N. For water basins of eight seas, we present the chemical compositions of the water-soluble aerosol fraction (ions, elements) and small gas-phase species, as well as estimates of their vertical fluxes. It is shown that substances are mainly (75-89 %) supplied from the atmosphere to the sea

  13. Spatial and temporal distributions of aerosol concentrations and depositions in Asia during the year 2010.

    PubMed

    Park, Soon-Ung; Lee, In-Hye; Joo, Seung Jin

    2016-01-15

    Aerosol Modeling System (AMS) that is consisted of the Asian Dust Aerosol Model2 (ADAM2) and the Community Multi-scale Air Quality (CMAQ) modeling system has been employed to document the spatial distributions of the monthly and the annual averaged concentration of both the Asian dust (AD) aerosol and the anthropogenic aerosol (AA), and their total depositions in the Asian region for the year 2010. It is found that the annual mean surface aerosol (PM10) concentrations in the Asian region affect in a wide region as a complex mixture of AA and AD aerosols; they are predominated by the AD aerosol in the AD source region of northern China and Mongolia with a maximum concentration exceeding 300 μg m(-3); AAs are predominated in the high pollutant emission regions of southern and eastern China and northern India with a maximum concentration exceeding 110 μg m(-3); while the mixture of AA and AD aerosols is dominated in the downwind regions extending from the Yellow Sea to the Northwest Pacific Ocean. It is also found that the annual total deposition of aerosols in the model domain is found to be 485 Tg (372 Tg by AD aerosol and 113 Tg by AA), of which 66% (319 Tg) is contributed by the dry deposition (305 Tg by AD aerosol and 14 Tg by AA) and 34% (166 Tg) by the wet deposition (66 Tg by AD aerosol and 100 Tg by AA), suggesting about 77% of the annual total deposition being contributed by the AD aerosol mainly through the dry deposition process and 24% of it by AA through the wet deposition process. The monthly mean aerosol concentration and the monthly total deposition show a significant seasonal variation with high in winter and spring, and low in summer.

  14. On measurements of aerosol-gas composition of the atmosphere during two expeditions in 2013 along Northern Sea Route

    NASA Astrophysics Data System (ADS)

    Sakerin, S. M.; Bobrikov, A. A.; Bukin, O. A.; Golobokova, L. P.; Pol'kin, Vas. V.; Pol'kin, Vik. V.; Shmirko, K. A.; Kabanov, D. M.; Khodzher, T. V.; Pavlov, A. N.; Potemkin, V. L.; Radionov, V. F.

    2015-06-01

    We presented the results of expedition measurements of the set of physical-chemical characteristics of atmospheric aerosol in water basins of Arctic and Far East seas, performed onboard RV Akademik Fedorov (17 August-22 September 2013) and RV Professor Khljustin (24 July-7 September 2013). The specific features of spatial distribution and time variations of aerosol optical depth (AOD) of the atmosphere in the wavelength range of 0.34-2.14 μm and boundary layer height, aerosol and black carbon mass concentrations, and disperse and chemical composition of aerosol are discussed. Over the Arctic Ocean (on the route of RV Akademik Fedorov) there is a decrease in aerosol and black carbon concentrations in northeastern direction: higher values were observed in the region of Spitsbergen and near the Kola Peninsula; and minimum values were observed at northern margins of the Laptev Sea. Average AOD (0.5 μm) values in this remote region were 0.03; the aerosol and black carbon mass concentrations were 875 and 22 ng m-3, respectively. The spatial distributions of most aerosol characteristics over Far East seas show their latitudinal decrease in the northern direction. On transit of RV Professor Khljustin from Japan to Chukchi Sea, the aerosol number concentration decreased, on the average, from 23.7 to 2.5 cm-3, the black carbon mass concentration decreased from 150 to 50 ng m-3, and AOD decreased from 0.19 to 0.03. We analyzed the variations in the boundary layer height, measured by ship-based lidar: the average value was 520 m, and the maximal value was 1200 m. In latitudinal distribution of the boundary layer height, there is a characteristic minimum at latitude of ∼ 55° N. For water basins of eight seas, we present the chemical compositions of water-soluble aerosol fraction (ions, elements) and small gaseous impurities, as well as estimates of their vertical fluxes. It is shown that substances are mainly (75-89 %) supplied from the atmosphere to the sea surface

  15. Determination of aerosol size distributions from spectral attenuation measurements.

    PubMed

    Grassl, H

    1971-11-01

    An iteration method for the determination of size distributions of aerosols from spectral attenuation data, similar to the one previously published for clouds, is presented. The basis for this iteration is to consider the extinction efficiency factor of particles as a set of weighting functions covering the entire radius region of a distribution. The weighting functions were calculated exactly from the Mie theory. Aerosol distributions are shown derived from tests with analytical size distributions and also generated from measured aerosol extinction data in seven spectral channels from 0.4-microto 10-micro wavelength in continental aerosols. The influence of relative humidity on the complex index of refraction is also discussed.

  16. Tropospheric aerosol size distributions simulated by three online global aerosol models using the M7 microphysics module

    SciTech Connect

    Zhang, Kai; Wan, Hui; Wang, Bin; Zhang, Meigen; Feichter, J.; Liu, Xiaohong

    2010-07-14

    Tropospheric aerosol size distributions are simulated by three online global models that employ exactly the same modal approach but differ in many aspects such as model meteorology, natural aerosol emissions, sulfur chemistry, and the parameterization of deposition processes. The main purpose of this study is to identify where the largest inter-model discrepancies occur and what the main reasons are. The number concentrations of different aerosol size ranges are compared among the three models and against observations. Overall all the three models can capture the basic features of the observed aerosol number spatial distributions. The magnitude of the number concentration of each mode is consistent among the three models. Quantitative differences are also clearly detectable. For the soluble and insoluble coarse mode and accumulation mode, inter-model discrepancies mainly result from differences in the sea salt and dust emissions, as well as the different strengths of the convective transport in the meteorological models. For the nucleation mode and the soluble Aitken mode, the spread of the model results is largest in the tropics and in the middle and upper troposphere. Diagnostics and sensitivity experiments suggest that this large spread is closely related to the sulfur cycle in the models, which is strongly affected by the choice of sulfur chemistry scheme, its coupling with the convective transport and wet deposition calculation, and the related meteorological fields such as cloud cover, cloud water content, and precipitation. The aerosol size distributions simulated by the three models are compared to observations in the boundary layer. The characteristic shape and magnitude of the distribution functions are reasonably reproduced in typical conditions (i.e., clean, polluted and transition areas). Biases in the mode parameters over the remote oceans and the China adjacent seas are probably caused by the fixed mode variance in the mathematical formulations used

  17. Global distribution of aerosols over the open ocean as derived from the Coastal Zone Color Scanner

    NASA Astrophysics Data System (ADS)

    Stegmann, P. M.; Tindale, N. W.

    1999-06-01

    Climatological maps of monthly mean aerosol radiance levels derived from the coastal zone color scanner (CZCS) were constructed for the world's ocean basins. This is the first study to use the 7.5-year CZCS data set to examine the distribution and seasonality of aerosols over the open ocean on a global scale. Examination of our satellite images found the most prominent large-scale patch of elevated aerosol radiances in each month off the coast of northwest Africa. The well-known, large-scale plumes of elevated aerosol levels in the Arabian Sea, the northwest Pacific, and off the east coast of North America were also successfully captured. Radiance data were extracted from 13 major open-ocean zones, ranging from the subpolar to equatorial regions. Results from these extractions revealed the aerosol load in both subpolar and subtropical zones to be higher in the Northern Hemisphere than in the Southern Hemisphere. Aerosol radiances in the subtropics of both hemispheres were about 2 times higher in summer than in winter. In subpolar regions, aerosol radiances in late spring/early summer were almost 3 times that observed in winter. In general, the aerosol signal was higher during the warmer months and lower during the cooler months, irrespective of location. A comparison between our mean monthly aerosol radiance maps with mean monthly chlorophyll maps (also from CZCS) showed similar seasonality between aerosol and chlorophyll levels in the subpolar zones of both hemispheres, i.e., high levels in summer, low levels in winter. In the subtropics of both hemispheres, however, chlorophyll levels were higher in winter months which coincided with a depressed aerosol signal. Our results indicate that the near-IR channel on ocean color sensors can be used to successfully capture well-known, large-scale aerosol plumes on a global scale and that future ocean color sensors may provide a platform for long-term synoptic studies of combined aerosol-phytoplankton productivity

  18. Global Distribution of Aerosols Over the Open Ocean as Derived from the Coastal Zone Color Scanner

    NASA Technical Reports Server (NTRS)

    Stegmann, P. M.; Tindale, N. W.

    1999-01-01

    Climatological maps of monthly mean aerosol radiance levels derived from the coastal zone color scanner (CZCS) were constructed for the world's ocean basins. This is the first study to use the 7.5.-year CZCS data set to examine the distribution and seasonality of aerosols over the open ocean on a global scale. Examination of our satellite images found the most prominent large-scale patch of elevated aerosol radiances in each month off the coast of northwest Africa. The well-known, large-scale plumes of elevated aerosol levels in the Arabian Sea, the northwest Pacific, and off the east coast of North America were also successfully captured. Radiance data were extracted from 13 major open-ocean zones, ranging from the subpolar to equatorial regions. Results from these extractions revealed the aerosol load in both subpolar and subtropical zones to be higher in the Northern Hemisphere than in the Southern Hemisphere. Aerosol radiances in the subtropics of both hemispheres were about 2 times higher in summer than in winter. In subpolar regions, aerosol radiances in late spring/early summer were almost 3 times that observed in winter. In general, the aerosol signal was higher during the warmer months and lower during the cooler months, irrespective of location. A comparison between our mean monthly aerosol radiance maps with mean monthly chlorophyll maps (also from CZCS) showed similar seasonality between aerosol and chlorophyll levels in the subpolar zones of both hemispheres, i.e., high levels in summer, low levels in winter. In the subtropics of both hemispheres, however, chlorophyll levels were higher in winter months which coincided with a depressed aerosol signal. Our results indicate that the near-IR channel on ocean color sensors can be used to successfully capture well-known, large-scale aerosol plumes on a global scale and that future ocean color sensors may provide a platform for long-term synoptic studies of combined aerosol-phytoplankton productivity

  19. Chemical composition of Eastern Black Sea aerosol--preliminary results.

    PubMed

    Balcılar, Ilker; Zararsız, Abdullah; Kalaycı, Yakup; Doğan, Güray; Tuncel, Gürdal

    2014-08-01

    Trace element composition of atmospheric particles collected at a high altitude site on the Eastern Black Sea coast of Turkey was investigated to understand atmospheric transport of pollutants to this semi-closed basin. Aerosol samples were collected at a timber-storage area, which is operated by the General Directorate of Forestry. The site is situated at a rural area and is approximately 50 km to the Black Sea coast and 200 km to the Georgia border of Turkey. Coarse (PM2.5-10) and fine (PM2.5) aerosol samples were collected between 2011 and 2013 using a "stacked filter unit". Collected samples were shipped to the Middle East Technical University in Ankara, where Na, Mg, Al, Si, S, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, As, Ba, Pb were measured by Energy dispersive x-ray fluorescence technique (EDXRF). Comparison of measured concentrations of elements with corresponding data generated at other parts of Turkey demonstrated that concentrations of pollution derived elements are higher at Eastern Black Sea than their corresponding concentrations measured at other parts of Turkey, which is attributed to frequent transport of pollutants from north wind sector. Positive matric factorization revealed four factors including three anthropogenic and a crustal factor. Southeastern parts of Turkey, Georgia and Black Sea coast of Ukraine were identified as source regions affecting composition of particles at our site, using trajectory statistics, namely "potential source contribution function" (PSCF). PMID:24373640

  20. Particle size distribution of indoor aerosol sources

    SciTech Connect

    Shah, K.B.

    1990-10-24

    As concern about Indoor Air Quality (IAQ) has grown in recent years, it has become necessary to determine the nature of particles produced by different indoor aerosol sources and the typical concentration that these sources tend to produce. These data are important in predicting the dose of particles to people exposed to these sources and it will also enable us to take effective mitigation procedures. Further, it will also help in designing appropriate air cleaners. A new state of the art technique, DMPS (Differential Mobility Particle Sizer) System is used to determine the particle size distributions of a number of sources. This system employs the electrical mobility characteristics of these particles and is very effective in the 0.01--1.0 {mu}m size range. A modified system that can measure particle sizes in the lower size range down to 3 nm was also used. Experimental results for various aerosol sources is presented in the ensuing chapters. 37 refs., 20 figs., 2 tabs.

  1. Global Aerosol Distributions Derived From the CALIPSO Observations

    NASA Astrophysics Data System (ADS)

    Kittaka, C.; Winker, D.; Omar, A.; Liu, Z.; Vaughan, M.; Trepte, C.

    2008-12-01

    Since June 2006, CALIPSO continues to provide routine and systematic measurements of lidar backscatter at two wavelengths, 532 and 1064 nm. As an active sensor, the quality of the measurement is nearly insensitive to surface properties allowing quantitative measurements in regions that are problematic to passive sensors. In particular, aerosol and cloud observations in the polar regions and desert areas are possible with the CALIPSO lidar through the different seasons of a year. The CALIPSO level 2 products, which include aerosol and cloud vertical profiles along tracks, reveal, for the first time, the multi-layer structure of aerosols and clouds on a global scale. This allows not only a depiction of aerosols in relation to clouds, but also the investigation of the interaction between aerosols and clouds. In this study, we present global distributions of aerosol in terms of season, layer height, aerosol species, and in relation to clouds using two years of CALIPSO observations. The CALIPSO aerosol extinction data sets under clear sky are evaluated against the AERONET aerosol optical depth (AOD) and the MODIS AOD collection 5 data sets. The agreement and discrepancies from these comparisons are characterized regionally and investigated using other CALIPSO observable and retrieved parameters. Furthermore, aerosols above clouds and in the vicinity of clouds are examined on a global scale. The implications for aerosol radiative forcing are discussed, highlighting the new and interesting aerosol features obtained from CALIPSO observations.

  2. Aerosol Behavior Log-Normal Distribution Model.

    2001-10-22

    HAARM3, an acronym for Heterogeneous Aerosol Agglomeration Revised Model 3, is the third program in the HAARM series developed to predict the time-dependent behavior of radioactive aerosols under postulated LMFBR accident conditions. HAARM3 was developed to include mechanisms of aerosol growth and removal which had not been accounted for in the earlier models. In addition, experimental measurements obtained on sodium oxide aerosols have been incorporated in the code. As in HAARM2, containment gas temperature, pressure,more » and temperature gradients normal to interior surfaces are permitted to vary with time. The effects of reduced density on sodium oxide agglomerate behavior and of nonspherical shape of particles on aerosol behavior mechanisms are taken into account, and aerosol agglomeration due to turbulent air motion is considered. Also included is a capability to calculate aerosol concentration attenuation factors and to restart problems requiring long computing times.« less

  3. Multiyear study of the dependence of sea salt aerosol on wind speed and sea ice conditions in the coastal Arctic

    NASA Astrophysics Data System (ADS)

    May, N. W.; Quinn, P. K.; McNamara, S. M.; Pratt, K. A.

    2016-08-01

    Thinning of Arctic sea ice gives rise to ice fracturing and leads (areas of open water surrounded by sea ice) that are a potential source of sea salt aerosol. Atmospheric particle inorganic ion concentrations, local sea ice conditions, and meteorology at Barrow, AK, from 2006 to 2009, were combined to investigate the dependence of submicron (aerodynamic diameter < 1 µm) and supermicron (aerodynamic diameter 1-10 µm) sea salt mass concentrations on sea ice coverage and wind speed. Consistent with a wind-dependent source, supermicron sea salt mass concentrations increased in the presence of nearby leads and wind speeds greater than 4 m s-1. Increased supermicron and submicron sea salt chloride depletion was observed for periods of low winds or a lack of nearby open water, consistent with transported sea salt influence. Sea salt aerosol produced from leads has the potential to alter cloud formation, as well as the chemical composition of the Arctic atmosphere and snowpack.

  4. Physic of the nucleon sea quark distributions

    NASA Astrophysics Data System (ADS)

    Vogt, R.

    Sea quark distributions in the nucleon have naively been expected to be generated perturbatively by gluon splitting. In this case, there is no reason for the light quark and anti-quark sea distributions to be different. No asymmetries in the strange or heavy quark sea distributions are predicted in the improved parton model. However, recent experiments have called these naive expectations into question. A violation of the Gottfried sum rule has been measured in several experiments, suggesting that overlineu < overlined in the proton. Additionally, other measurements, while not definitive, show that there may be an asymmetry in the strange and anti-strange quark sea distributions. These effects may require nonperturbative explanations. In this review we first discuss the perturbative aspects of the sea quark distributions. We then describe the experiments that could point to nonperturbative contributions to the nucleon sea. Current phenomenological models that could explain some of these effects are reviewed.

  5. Physics of the nucleon sea quark distributions

    SciTech Connect

    Vogt, R.

    2000-03-10

    Sea quark distributions in the nucleon have naively been expected to be generated perturbatively by gluon splitting. In this case, there is no reason for the light quark and anti-quark sea distributions to be different. No asymmetries in the strange or heavy quark sea distributions are predicted in the improved parton model. However,recent experiments have called these naive expectations into question. A violation of the Gottfried sum rule has been measured in several experiments, suggesting that (bar u) < (bar d) in the proton. Additionally, other measurements, while not definitive, show that there may be an asymmetry in the strange and anti-strange quark sea distributions. These effects may require nonperturbative explanations. In this review we first discuss the perturbative aspects of the sea quark distributions. We then describe the experiments that could point to nonperturbative contributions to the nucleon sea. Current phenomenological models that could explain some of these effects are reviewed.

  6. Multi-modal analysis of aerosol robotic network size distributions for remote sensing applications: dominant aerosol type cases

    NASA Astrophysics Data System (ADS)

    Taylor, M.; Kazadzis, S.; Gerasopoulos, E.

    2014-03-01

    To date, size distributions obtained from the aerosol robotic network (AERONET) have been fit with bi-lognormals defined by six secondary microphysical parameters: the volume concentration, effective radius, and the variance of fine and coarse particle modes. However, since the total integrated volume concentration is easily calculated and can be used as an accurate constraint, the problem of fitting the size distribution can be reduced to that of deducing a single free parameter - the mode separation point. We present a method for determining the mode separation point for equivalent-volume bi-lognormal distributions based on optimization of the root mean squared error and the coefficient of determination. The extracted secondary parameters are compared with those provided by AERONET's Level 2.0 Version 2 inversion algorithm for a set of benchmark dominant aerosol types, including desert dust, biomass burning aerosol, urban sulphate and sea salt. The total volume concentration constraint is then also lifted by performing multi-modal fits to the size distribution using nested Gaussian mixture models, and a method is presented for automating the selection of the optimal number of modes using a stopping condition based on Fisher statistics and via the application of statistical hypothesis testing. It is found that the method for optimizing the location of the mode separation point is independent of the shape of the aerosol volume size distribution (AVSD), does not require the existence of a local minimum in the size interval 0.439 μm ≤ r ≤ 0.992 μm, and shows some potential for optimizing the bi-lognormal fitting procedure used by AERONET particularly in the case of desert dust aerosol. The AVSD of impure marine aerosol is found to require three modes. In this particular case, bi-lognormals fail to recover key features of the AVSD. Fitting the AVSD more generally with multi-modal models allows automatic detection of a statistically significant number of aerosol

  7. Simulation of aerosol chemical compositions in the Western Mediterranean Sea

    NASA Astrophysics Data System (ADS)

    Chrit, Mounir; Kata Sartelet, Karine; Sciare, Jean; Marchand, Nicolas; Pey, Jorge; Sellegri, Karine

    2016-04-01

    This work aims at evaluating the chemical transport model (CTM) Polair3d of the air-quality modelling platform Polyphemus during the ChArMex summer campaigns of 2013, using ground-based measurements performed at ERSA (Cape Corsica, France), and at determining the processes controlling organic aerosol concentrations at ERSA. Simulations are compared to measurements for concentrations of both organic and inorganic species, as well as the ratio of biogenic versus anthropogenic particles, and organic aerosol properties (oxidation state). For inorganics, the concentrations of sulphate, sodium, chloride, ammonium and nitrate are compared to measurements. Non-sea-salt sulphate and ammonium concentrations are well reproduced by the model. However, because of the geographic location of the measurement station at Cape Corsica which undergoes strong wind velocities and sea effects, sea-salt sulphate, sodium, chloride and nitrate concentrations are strongly influenced by the parameterizations used for sea-salt emissions. Different parameterizations are compared and a parameterization is chosen after comparison to sodium measurements. For organics, the concentrations are well modelled when compared to experimental values. Anthropogenic particles are influenced by emission of semi-volatile organic compounds (SVOC). Measurements allow us to refine the estimation of those emissions, which are currently missing in emission inventories. Although concentrations of biogenic particles are well simulated, the organic chemical compounds are not enough oxidised in the model. The observed oxidation state of organics shows that the oligomerisation of pinonaldehyde was over-estimated in Polyphemus. To improve the oxidation property of organics, the formation of extremely low volatile organic compounds from autoxidation of monoterpenes is added to Polyphemus, using recently published data from chamber experiments. These chemical compounds are highly oxygenated and are formed rapidly, as first

  8. Preliminary Evaluation of GEOS-5 Aerosol and CO Distributions Forecast During TC4

    NASA Technical Reports Server (NTRS)

    Colarco, Peter R.

    2007-01-01

    The NASA Tropical Composition, Cloud, and Climate Coupling (TC4) Mission was based out San Jose, Costa Rica during July and August 2007. During TC4 the NASA Global Modeling and Assimilation Office (GMAO) ran twice-daily 0.5 x 0.666 global 5-day forecasts of the Goddard Earth Observing System atmospheric general circulation model and data assimilation system (GEOS-5). This implementation of GEOS-5 contained an aerosol and carbon monoxide (CO) model to provide online forecast tropospheric distributions of dust, sea salt, sulfate, and carbonaceous aerosols and CO for both the planning of flights and for science. Here we provide a description of the aerosol and CO modeling system and give a preliminary evaluation of forecast tracer distributions. Our comparisons to satellite observations of aerosol and CO show qualitatively similar simulated distributions of tracers to those observed. During TC4 copious amounts of dust were observed in the Caribbean. The model generally reproduced the observations of the timing of dust events and the vertical structure in the lower atmosphere. However, the model simulations had too much aerosol at high altitudes relative to airborne Cloud Physics Lidar observations. The results were similar for biomass burning aerosol and CO tracers, where the model showed higher simulated concentrations of these tracers at aircraft flight altitude than observations.

  9. Effect of aerosol vertical distribution on aerosol-radiation interaction: A theoretical prospect.

    PubMed

    Mishra, Amit Kumar; Koren, Ilan; Rudich, Yinon

    2015-10-01

    This study presents a theoretical investigation of the effect of the aerosol vertical distribution on the aerosol radiative effect (ARE). Four aerosol composition models (dust, polluted dust, pollution and pure scattering aerosols) with varying aerosol vertical profiles are incorporated into a radiative transfer model. The simulations show interesting spectral dependence of the ARE on the aerosol layer height. ARE increases with the aerosol layer height in the ultraviolet (UV: 0.25-0.42 μm) and thermal-infrared (TH-IR: 4.0-20.0 μm) regions, whereas it decreases in the visible-near infrared (VIS-NIR: 0.42-4.0 μm) region. Changes in the ARE with aerosol layer height are associated with different dominant processes for each spectral region. The combination of molecular (Rayleigh) scattering and aerosol absorption is the key process in the UV region, whereas aerosol (Mie) scattering and atmospheric gaseous absorption are key players in the VIS-NIR region. The longwave emission fluxes are controlled by the environmental temperature at the aerosol layer level. ARE shows maximum sensitivity to the aerosol layer height in the TH-IR region, followed by the UV and VIS-NIR regions. These changes are significant even in relatively low aerosol loading cases (aerosol optical depth ∼0.2-0.3). Dust aerosols are the most sensitive to altitude followed by polluted dust and pollution in all three different wavelength regions. Differences in the sensitivity of the aerosol type are explained by the relative strength of their spectral absorption/scattering properties. The role of surface reflectivity on the overall altitude dependency is shown to be important in the VIS-NIR and UV regions, whereas it is insensitive in the TH-IR region. Our results indicate that the vertical distribution of water vapor with respect to the aerosol layer is an important factor in the ARE estimations. Therefore, improved estimations of the water vapor profiles are needed for the further reduction in

  10. Effect of aerosol vertical distribution on aerosol-radiation interaction: A theoretical prospect.

    PubMed

    Mishra, Amit Kumar; Koren, Ilan; Rudich, Yinon

    2015-10-01

    This study presents a theoretical investigation of the effect of the aerosol vertical distribution on the aerosol radiative effect (ARE). Four aerosol composition models (dust, polluted dust, pollution and pure scattering aerosols) with varying aerosol vertical profiles are incorporated into a radiative transfer model. The simulations show interesting spectral dependence of the ARE on the aerosol layer height. ARE increases with the aerosol layer height in the ultraviolet (UV: 0.25-0.42 μm) and thermal-infrared (TH-IR: 4.0-20.0 μm) regions, whereas it decreases in the visible-near infrared (VIS-NIR: 0.42-4.0 μm) region. Changes in the ARE with aerosol layer height are associated with different dominant processes for each spectral region. The combination of molecular (Rayleigh) scattering and aerosol absorption is the key process in the UV region, whereas aerosol (Mie) scattering and atmospheric gaseous absorption are key players in the VIS-NIR region. The longwave emission fluxes are controlled by the environmental temperature at the aerosol layer level. ARE shows maximum sensitivity to the aerosol layer height in the TH-IR region, followed by the UV and VIS-NIR regions. These changes are significant even in relatively low aerosol loading cases (aerosol optical depth ∼0.2-0.3). Dust aerosols are the most sensitive to altitude followed by polluted dust and pollution in all three different wavelength regions. Differences in the sensitivity of the aerosol type are explained by the relative strength of their spectral absorption/scattering properties. The role of surface reflectivity on the overall altitude dependency is shown to be important in the VIS-NIR and UV regions, whereas it is insensitive in the TH-IR region. Our results indicate that the vertical distribution of water vapor with respect to the aerosol layer is an important factor in the ARE estimations. Therefore, improved estimations of the water vapor profiles are needed for the further reduction in

  11. Characterization of particleboard aerosol - size distribution and formaldehyde content

    SciTech Connect

    Stumpf, J.M.; Blehm, K.D.; Buchan, R.M.; Gunter, B.J.

    1986-12-01

    Health hazards unique to particleboard include the generation of urea-formaldehyde resin bound in wood aerosol and release of formaldehyde gas that can be inhaled by the worker. A particleboard aerosol was generated by a sanding process and collected under laboratory conditions that determined the particle size distribution and formaldehyde content. Three side-by-side Marple 296 personal cascade impactors with midget impingers attached downstream collected particleboard aerosol and gaseous formaldehyde for ten sample runs. Gravimetric analysis quantified the collected aerosol mass, and chromotropic acid/spectrophotometric analytical methods were employed for formaldehyde content in particleboard aerosol and gaseous formaldehyde liberated from sanded particleboard. Significant variations (p<.005) were observed for the particleboard mass and gaseous formaldehyde collected between sample runs. No significant differences (..cap alpha.. = .05) were observed for the aerosol size distribution determined and formaldehyde content in particle board aerosol per unit mass for sampling trials. The overall MMAD of particleboard aerosol was 8.26 ..mu..mAED with a sigmag of 2.01. A predictive model was derived for determining the expected formaldehyde content (..mu..g) by particleboard aerosol mass (mg) collected and particulate size (..mu..mAED).

  12. Physicochemical properties of aerosols over the northeast Atlantic: Evidence for wind-speed-related submicron sea-salt aerosol production

    SciTech Connect

    O'Dowd, C.D.; Smith, M.H. )

    1993-01-20

    Physicochemical characteristics of submicron aerosol particles over the Northeast Atlantic (63[degrees]N, 8[degrees]W) during October/November 1989 have been examined using a thermal analytical technique and are classified according 10 air mass origin. Aerosol associated with anthropogenically influenced air masses contained typically 80% sulphate particles by number, the remainder being soot carbon and sea salt. For Arctic air masses the contribution of sulphate to the total aerosol was reduced to around 65%, due to low concentrations relative 10 sea salt which is dependent on wind speed. In situations with clean maritime air and high wind speeds, sulphate aerosol accounted for less than 25% of the total accumulation mode particles, the remainder consisting predominantly of sea salt. Arctic air masses and clean maritime air during periods of high winds were consistently acidic with inferred molar ratios of NH[sub 4][sup +]/SO[sub 4][sup =] near 0.2. The continental and modified maritime aerosol encountered was found to have molar ratios of about 0.8. Soot carbon was present in all air masses to a similar degree (5-13%). In clean air masses, submicron sea salt aerosol concentrations showed a strong exponential increase with wind speed (correlation coefficients cc [ge] 0.8), down to a dry particle radius of 0.05 [mu]m. Under these clean air' conditions and high winds the sea salt aerosol dominated all particle sizes for r > 0.05 [mu]m and accounted for approximately 75% of the total concentration, suggesting that under these conditions, sea salt aerosol would comprise the primary source cloud condensation nuclei (CCN) in stratiform clouds. 30 refs., 8 figs., 4 tabs.

  13. Chemical distribution in high-solids paint overspray aerosols.

    PubMed

    D'Arcy, J B; Chan, T L

    1990-03-01

    The chemical composition of high-solids basecoat paint overspray aerosols was determined as a function of particle size. Detailed information on the chemical composition of the overspray aerosols is important in health hazard evaluation since the composition and distribution within the airborne particles may differ significantly from the bulk paint material. This study was conducted in a typical down-draft paint booth equipped with air-atomized spray painting equipment. A fixed paint target was used to simulate typical overspray generation conditions and the aerosols were collected isokinetically with a seven-stage cascade impactor for size-fractionated analysis. The overspray aerosol from six paints consisted of organic paint binders with varying amounts of inorganic species as pigments or luster enhancers. These overspray aerosols had mass median aerodynamic diameters (MMAD) ranging from 2.9 to 9.7 microns. The size-fractionated paint samples collected on the impaction stages were analyzed by energy dispersive X-ray spectrometry on a scanning electron microscope (SEM-EDXRS) to identify the metallic elements. Atomic absorption spectrometry was used to determine the mass distribution of aluminum and iron as indicators of nonuniform distribution. Three of the aerosols containing aluminum were found to have bimodal distributions with most aluminum distributions having cumulative MMADs larger than the total aerosol. Iron in the aerosols was bimodal for three of the paints with all samples having an overall iron MMAD less than or equal to the overspray aerosol MMAD. Analysis using ultraviolet spectrometry revealed that the organic compounds present in the size-fractionated particulate samples consisted of a single, polydispersed mode with an MMAD similar to that of the total overspray aerosol.(ABSTRACT TRUNCATED AT 250 WORDS) PMID:2327324

  14. Chemical distribution in high-solids paint overspray aerosols

    SciTech Connect

    D'Arcy, J.B.; Chan, T.L. )

    1990-03-01

    The chemical composition of high-solids basecoat paint overspray aerosols was determined as a function of particle size. Detailed information on the chemical composition of the overspray aerosols is important in health hazard evaluation since the composition and distribution within the airborne particles may differ significantly from the bulk paint material. This study was conducted in a typical down-draft paint booth equipped with air-atomized spray painting equipment. A fixed paint target was used to simulate typical overspray generation conditions and the aerosols were collected isokinetically with a seven-stage cascade impactor for size-fractionated analysis. The overspray aerosol from six paints consisted of organic paint binders with varying amounts of inorganic species as pigments or luster enhancers. These overspray aerosols had mass median aerodynamic diameters (MMAD) ranging from 2.9 to 9.7 microns. The size-fractionated paint samples collected on the impaction stages were analyzed by energy dispersive X-ray spectrometry on a scanning electron microscope (SEM-EDXRS) to identify the metallic elements. Atomic absorption spectrometry was used to determine the mass distribution of aluminum and iron as indicators of nonuniform distribution. Three of the aerosols containing aluminum were found to have bimodal distributions with most aluminum distributions having cumulative MMADs larger than the total aerosol. Iron in the aerosols was bimodal for three of the paints with all samples having an overall iron MMAD less than or equal to the overspray aerosol MMAD. Analysis using ultraviolet spectrometry revealed that the organic compounds present in the size-fractionated particulate samples consisted of a single, polydispersed mode with an MMAD similar to that of the total overspray aerosol.

  15. Direct aerosol chemical composition measurements to evaluate the physicochemical differences between controlled sea spray aerosol generation schemes

    NASA Astrophysics Data System (ADS)

    Collins, D. B.; Zhao, D. F.; Ruppel, M. J.; Laskina, O.; Grandquist, J. R.; Modini, R. L.; Stokes, M. D.; Russell, L. M.; Bertram, T. H.; Grassian, V. H.; Deane, G. B.; Prather, K. A.

    2014-11-01

    Controlled laboratory studies of the physical and chemical properties of sea spray aerosol (SSA) must be under-pinned by a physically and chemically accurate representation of the bubble-mediated production of nascent SSA particles. Bubble bursting is sensitive to the physico-chemical properties of seawater. For a sample of seawater, any important differences in the SSA production mechanism are projected into the composition of the aerosol particles produced. Using direct chemical measurements of SSA at the single-particle level, this study presents an intercomparison of three laboratory-based, bubble-mediated SSA production schemes: gas forced through submerged sintered glass filters ("frits"), a pulsed plunging-waterfall apparatus, and breaking waves in a wave channel filled with natural seawater. The size-resolved chemical composition of SSA particles produced by breaking waves is more similar to particles produced by the plunging waterfall than those produced by sintered glass filters. Aerosol generated by disintegrating foam produced by sintered glass filters contained a larger fraction of organic-enriched particles and a different size-resolved elemental composition, especially in the 0.8-2 μm dry diameter range. Interestingly, chemical differences between the methods only emerged when the particles were chemically analyzed at the single-particle level as a function of size; averaging the elemental composition of all particles across all sizes masked the differences between the SSA samples. When dried, SSA generated by the sintered glass filters had the highest fraction of particles with spherical morphology compared to the more cubic structure expected for pure NaCl particles produced when the particle contains relatively little organic carbon. In addition to an intercomparison of three SSA production methods, the role of the episodic or "pulsed" nature of the waterfall method on SSA composition was under-taken. In organic-enriched seawater, the continuous

  16. 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

  17. A global model study of processes controlling aerosol size distributions in the Arctic spring and summer

    NASA Astrophysics Data System (ADS)

    Korhonen, Hannele; Carslaw, Kenneth S.; Spracklen, Dominick V.; Ridley, David A.; StröM, Johan

    2008-04-01

    We use a global chemical transport model (CTM) with size-resolved aerosol microphysics to evaluate our understanding of the processes that control Arctic aerosol, focussing on the seasonal changes in the particle size distribution during the transition from Arctic haze in spring to cleaner conditions in summer. This period presents several challenges for a global model simulation because of changes in meteorology, which affect transport pathways and precipitation scavenging rates, changes in the ocean-atmosphere flux of trace gases and particulates associated with sea ice break-up and increased biological activity, and changes in photolysis and oxidation rates which can affect particle nucleation and growth rates. Observations show that these changes result in a transition from an accumulation mode-dominated aerosol in spring to one dominated by Aitken and nucleation mode particles in summer. We find that remote Arctic aerosol size distribution is very sensitive to the model treatment of wet removal. In order to simulate the high accumulation mode concentrations typical of winter and spring it was necessary to substantially reduce the scavenging of these particles during transport. The resulting increases in accumulation mode lead to improvement in the modeled Aitken mode particle concentrations (which fall, due to increased scavenging in the free troposphere) and produce aerosol optical depths in good agreement with observations. The summertime increase in nucleation and Aitken mode particles is consistent with changes in local aerosol nucleation rates driven mainly by increased photochemical production of sulphuric acid vapor and, to a lesser extent, by decreases in the condensation sink as Arctic haze decreases. Alternatively, to explain the observed summertime Aitken mode particle concentrations in terms of ultrafine sea spray particles requires a sea-air flux a factor 5-25greater than predicted by current wind speed and sea surface temperature dependent flux

  18. Temporal variability of aerosol optical thickness vertical distribution observed from CALIOP

    NASA Astrophysics Data System (ADS)

    Toth, Travis D.; Zhang, Jianglong; Campbell, James R.; Reid, Jeffrey S.; Vaughan, Mark A.

    2016-08-01

    Temporal variability in the vertical distribution of aerosol optical thickness (AOT) derived from the 0.532 µm aerosol extinction coefficient is described using Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP) observations over 8.5 years (June 2006 to December 2014). Temporal variability of CALIOP column-integrated AOT is largely consistent with total column AOT trends from several passive satellite sensors, such as the Moderate Resolution Imaging Spectroradiometer, Multiangle Imaging Spectroradiometer, and the Sea-viewing Wide Field-of-view Sensor. Globally, a 0.0002 AOT per year positive trend in deseasonalized CALIOP total column AOT for daytime conditions is attributed to corresponding changes in near-surface (i.e., 0.0-0.5 km or 0.5-1.0 km above ground level (agl)) aerosol particle loading, while a -0.0006 AOT per year trend during nighttime is attributed to elevated (i.e., 1.0-2.0 km or >2.0 km agl) aerosols. Regionally, increasing daytime CALIOP AOTs are found over Southern Africa and India, mostly due to changes in aerosol loading at the 1.0-2.0 km and 0.0-0.5 km agl layers, respectively. Decreasing daytime CALIOP AOTs are observed over Northern Africa, Eastern U.S., and South America (due mostly to elevated aerosol loading), while the negative CALIOP AOT trends found over Eastern China, Europe, and Western U.S. are due mostly to aerosol layers nearer the surface. To our knowledge, this study is the first to provide both a globally comprehensive estimation of the temporal variation in aerosol vertical distribution and an insight into passive sensor column AOT trends in the vertical domain.

  19. Phytoplankton blooms weakly influence the cloud forming ability of sea spray aerosol

    NASA Astrophysics Data System (ADS)

    Collins, Douglas B.; Bertram, Timothy H.; Sultana, Camille M.; Lee, Christopher; Axson, Jessica L.; Prather, Kimberly A.

    2016-09-01

    After many field studies, the establishment of connections between marine microbiological processes, sea spray aerosol (SSA) composition, and cloud condensation nuclei (CCN) has remained an elusive challenge. In this study, we induced algae blooms to probe how complex changes in seawater composition impact the ability of nascent SSA to act as CCN, quantified by using the apparent hygroscopicity parameter (κapp). Throughout all blooms, κapp ranged between 0.7 and 1.4 (average 0.95 ± 0.15), consistent with laboratory investigations using algae-produced organic matter, but differing from climate model parameterizations and in situ SSA generation studies. The size distribution of nascent SSA dictates that changes in κapp associated with biological processing induce less than 3% change in expected CCN concentrations for typical marine cloud supersaturations. The insignificant effect of hygroscopicity on CCN concentrations suggests that the SSA production flux and/or secondary aerosol chemistry may be more important factors linking ocean biogeochemistry and marine clouds.

  20. Tropospheric aerosols: size-differentiated chemistry and large-scale spatial distributions.

    PubMed

    Hidy, George M; Mohnen, Volker; Blanchard, Charles L

    2013-04-01

    Worldwide interest in atmospheric aerosols has emerged since the late 20th century as a part of concerns for air pollution and radiative forcing of the earth's climate. The use of aircraft and balloons for sampling and the use of remote sensing have dramatically expanded knowledge about tropospheric aerosols. Our survey gives an overview of contemporary tropospheric aerosol chemistry based mainly on in situ measurements. It focuses on fine particles less than 1-2.5 microm in diameter. The physical properties of particles by region and altitude are exemplified by particle size distributions, total number and volume concentration, and optical parameters such as extinction coefficient and aerosol optical depth. Particle chemical characterization is size dependent, differentiated by ubiquitous sulfate, and carbon, partially from anthropogenic activity. Large-scale particle distributions extend to intra- and intercontinental proportions involving plumes from population centers to natural disturbances such as dust storms and vegetation fires. In the marine environment, sea salt adds an important component to aerosols. Generally, aerosol components, most of whose sources are at the earth's surface, tend to dilute and decrease in concentration with height, but often show different (layered) profiles depending on meteorological conditions. Key microscopic processes include new particle formation aloft and cloud interactions, both cloud initiation and cloud evaporation. Measurement campaigns aloft are short term, giving snapshots of inherently transient phenomena in the troposphere. Nevertheless, these data, combined with long-term data at the surface and optical depth and transmission observations, yield a unique picture of global tropospheric particle chemistry. PMID:23687724

  1. Simulating SAL formation and aerosol size distribution during SAMUM-I

    NASA Astrophysics Data System (ADS)

    Khan, Basit; Stenchikov, Georgiy; Weinzierl, Bernadett; Kalenderski, Stoitchko; Osipov, Sergey

    2015-04-01

    To understand the formation mechanisms of Saharan Air Layer (SAL), we combine model simulations and dust observations collected during the first stage of the Saharan Mineral Dust Experiment (SAMUM-I), which sampled dust events that extended from Morocco to Portugal, and investigated the spatial distribution and the microphysical, optical, chemical, and radiative properties of Saharan mineral dust. We employed the Weather Research Forecast model coupled with the Chemistry/Aerosol module (WRF-Chem) to reproduce the meteorological environment and spatial and size distributions of dust. The experimental domain covers northwest Africa including the southern Sahara, Morocco and part of the Atlantic Ocean with 5 km horizontal grid spacing and 51 vertical layers. The experiments were run from 20 May to 9 June 2006, covering the period of most intensive dust outbreaks. Comparisons of model results with available airborne and ground-based observations show that WRF-Chem reproduces observed meteorological fields as well as aerosol spatial distribution across the entire region and along the airplane's tracks. We evaluated several aerosol uplift processes and found that orographic lifting, aerosol transport through the land/sea interface with steep gradients of meteorological characteristics, and interaction of sea breezes with the continental outflow are key mechanisms that form a surface-detached aerosol plume over the ocean. Comparisons of simulated dust size distributions with airplane and ground-based observations are generally good, but suggest that more detailed treatment of microphysics in the model is required to capture the full-scale effect of large aerosol particles.

  2. Variations in hygroscopic growth of sub- and super-micron sea spray aerosols during a phytoplankton bloom

    NASA Astrophysics Data System (ADS)

    Forestieri, S.; Jayarathne, T. S.; Stone, E. A.; Laskina, O.; Grassian, V. H.; Lee, C.; Sultana, C. M.; Moore, K.; Cornwell, G.; Novak, G.; Bertram, T. H.; Prather, K. A.; Cappa, C. D.

    2014-12-01

    Marine sea spray aerosols (SSA) make up an important portion of natural aerosols (prior to anthropogenic influence) and are therefore important in establishing the baseline for anthropogenic aerosol climate impacts. One way aerosols impact climate is by scattering solar radiation, and how much light is scattered depends upon the size of aerosols. Aerosols grow larger via water uptake and thus scatter more light at elevated relative humidities. This growth depends on composition. SSA can become enriched in organics during phytoplankton blooms, becoming less salty and therefore less hygroscopic. Aerosol hygroscopicity of SSA sampled during an in-lab phytoplankton bloom were measured during the CAICE-IMPACTS 2014 study. SSA were generated via breaking waves in an enclosed 33 m wave channel filled with natural seawater. Aerosol hygroscopicity was characterized by measuring light extinction at 532 nm of dry aerosols and of aerosols humidified to 85% relative humidity using a Cavity Ringdown Spectrometer. These optical growth factors (humidified extinction/dry extinction) were converted to physical growth factors using Mie Theory calculations and aerosol size distributions measured with a scanning electrical mobility spectrometer (SEMS) and an aerodynamic particle sizer (APS). Growth factors for super- and sub-micron SSA were quantified separately through the use of a PM2.5 cyclone or PM1 impactor. The observed SSA growth factors will be linked to SSA and source water chemical composition determined by both offline and online analysis of samples. The SSA bulk growth factors will also be compared with concurrent measurements of the efficiency with which SSA act as cloud condensation nuclei. Observed SSA growth factors will also be compared to offline hygroscopic growth measurements.

  3. Dynamic Singularity Spectrum Distribution of Sea Clutter

    NASA Astrophysics Data System (ADS)

    Xiong, Gang; Yu, Wenxian; Zhang, Shuning

    2015-12-01

    The fractal and multifractal theory have provided new approaches for radar signal processing and target-detecting under the background of ocean. However, the related research mainly focuses on fractal dimension or multifractal spectrum (MFS) of sea clutter. In this paper, a new dynamic singularity analysis method of sea clutter using MFS distribution is developed, based on moving detrending analysis (DMA-MFSD). Theoretically, we introduce the time information by using cyclic auto-correlation of sea clutter. For transient correlation series, the instantaneous singularity spectrum based on multifractal detrending moving analysis (MF-DMA) algorithm is calculated, and the dynamic singularity spectrum distribution of sea clutter is acquired. In addition, we analyze the time-varying singularity exponent ranges and maximum position function in DMA-MFSD of sea clutter. For the real sea clutter data, we analyze the dynamic singularity spectrum distribution of real sea clutter in level III sea state, and conclude that the radar sea clutter has the non-stationary and time-varying scale characteristic and represents the time-varying singularity spectrum distribution based on the proposed DMA-MFSD method. The DMA-MFSD will also provide reference for nonlinear dynamics and multifractal signal processing.

  4. Case study of absorption aerosol optical depth closure of black carbon over the East China Sea

    NASA Astrophysics Data System (ADS)

    Koike, M.; Moteki, N.; Khatri, P.; Takamura, T.; Takegawa, N.; Kondo, Y.; Hashioka, H.; Matsui, H.; Shimizu, A.; Sugimoto, N.

    2014-01-01

    aerosol optical depth (AAOD) measurements made by sun-sky photometers are currently the only constraint available for estimates of the global radiative forcing of black carbon (BC), but their validation studies are limited. In this paper, we report the first attempt to compare AAODs derived from single-particle soot photometer (SP2) and ground-based sun-sky photometer (sky radiometer, SKYNET) measurements. During the Aerosol Radiative Forcing in East Asia (A-FORCE) experiments, BC size distribution and mixing state vertical profiles were measured using an SP2 on board a research aircraft near the Fukue Observatory (32.8°N, 128.7°E) over the East China Sea in spring 2009 and late winter 2013. The aerosol extinction coefficients (bext) and single scattering albedo (SSA) at 500 nm were calculated based on aerosol size distribution and detailed BC mixing state information. The calculated aerosol optical depth (AOD) agreed well with the sky radiometer measurements (2 ± 6%) when dust loadings were low (lidar-derived nonspherical particle contribution to AOD less than 20%). However, under these low-dust conditions, the AAODs obtained from sky radiometer measurements were only half of the in situ estimates. When dust loadings were high, the sky radiometer measurements showed systematically higher AAODs even when all coarse particles were assumed to be dust for in situ measurements. These results indicate that there are considerable uncertainties in AAOD measurements. Uncertainties in the BC refractive index, optical calculations from in situ data, and sky radiometer retrieval analyses are discussed.

  5. Particle size distributions of several commonly used seeding aerosols

    NASA Technical Reports Server (NTRS)

    Crosswy, F. L.

    1985-01-01

    During the course of experimentation, no solid particle powder could be found which produced an aerosol with a narrow particle size distribution when fluidization was the only flow process used in producing the aerosol. The complication of adding particle size fractionation processes to the aerosol generation effort appears to be avoidable. In this regard, a simple sonic orifice is found to be effective in reducing the percentage of agglomerates in the several metal oxide powders tested. Marginally beneficial results are obtained for a 0.5/99.5 percent by weight mixture of the flow agent and metal oxide powder. However, agglomeration is observed to be enhanced when the flow agent percentage is increased to 5 percent. Liquid atomization using the Collison nebulizer as well as a version of the Laskin nozzle resulted in polydispersed aerosols with particle size distributions heavily weighted by the small particle end of the size spectrum. The aerosol particle size distributions produced by the vaporization/condensation seeder are closer to the ideal monodispersed aerosol than any of the other aerosols tested. In addition, this seeding approach affords a measure of control over particle size and particle production rate.

  6. Sulfate aerosol distributions and cloud variations during El Nino anomalies

    SciTech Connect

    Parungo, F. ); Hicks, B. )

    1993-02-20

    The effects of aerosols on cloud characteristics, albedo, rainfall amount, and overall climate changes were investigated by assessing the qualitative associations and quantitative correlations between the relevant variables during El Nino-Southern Oscillation (ENSO) perturbations. Both historical records and data from recent field measurements for the Pacific Ocean region were used for the investigation. The results show that ENSO perturbations could change sulfate aerosol production and distribution over the surveyed regions. Strong correlations were observed between condensation nucleus concentrations and sulfate aerosol concentrations, and between cloud amount and albedo. Weak but significant correlations were also observed between condensation nucleus concentrations and cloud amounts, and between sulfate aerosol concentrations and rainfall amounts. Although sulfate aerosols appeared to have a strong impact on cloud microphysics, the present data confirm that cloud dynamics play the pivotal role in control of cloud types and cloud amount in the studied regions. 31 refs., 5 figs., 3 tabs.

  7. Sea salt aerosol from blowing snow on sea ice - modeling vs observation

    NASA Astrophysics Data System (ADS)

    Yang, Xin; Frey, Markus; Norris, Sarah; Brooks, Ian; Anderson, Philip; Jones, Anna; wolff, Eric; Legrand, Michel

    2016-04-01

    Blowing snow over sea ice, through a subsequent sublimation process of salt-containing blown snow particles, has been hypothesized as a significant sea salt aerosol (SSA) source in high latitudes. This mechanism has been strongly supported by a winter cruise in the Weddell Sea (during June-August 2013). The newly collected data, including both physical and chemical components, provide a unique way to test and validate the parameterisation used for describing the SSA production from blowing snow events. With updates to some key parameters such as snow salinity in a global Chemistry-transport model pTOMCAT, simulated SSA concentrations can be well compared with measured SSA data. In this presentation, I will report modeled SSA number density against collected data on board of Polarstern ship during the Weddell Sea cruise, as well as modeled SSA massive concentrations against those measured at both coastal sites such as Alert in the North and Dumont d'Urville (DDU) in the South and central Antarctic sites such as Concordia and Kohnen stations. Model experiments indicated that open ocean-sourced SSA could not explain the observed winter SSA peaks seen in most polar sites, while with sea ice-sourced SSA in the model, the winter peaks can be well improved indicating the importance of sea ice-sourced SSA as a significant contributor to the salts (Na+, Cl-) recorded in the ice core.

  8. The regional distribution characteristics of aerosol optical depth over the Tibetan Plateau

    NASA Astrophysics Data System (ADS)

    Xu, Chao; Ma, Yaoming; You, Chao; Zhu, Zhikun

    2016-04-01

    The Tibetan Plateau (TP) is representative of typical clean atmospheric conditions. Aerosol optical depth (AOD) retrieved by Multi-angle Imaging SpectroRadiometer (MISR) is higher over Qaidam Basin than the rest of the TP all the year. Different monthly variation patterns of AOD are observed over the southern and northern TP, whereby the aerosol load is usually higher in the northern TP than in the southern part. The aerosol load over the northern part increases from April to June, peaking in May. The maximum concentration of aerosols over the southern TP occurs in July. Aerosols appear to be more easily transported to the main body of the TP across the northern edge rather than the southern edge. This is may be partly because the altitude is lower at the northern edge than that of the Himalayas located along the southern edge of the TP. Three-dimensional distributions of dust, polluted dust, polluted continental and smoke are also investigated based on Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observation (CALIPSO) data. Dust is found to be the most prominent aerosol type on the TP, and other types of aerosols affect the atmospheric environment slightly. A dividing line of higher dust occurrence in the northern TP and lower dust occurrence in the southern TP can be observed clearly at altitude of 6-8 km above sea level, especially in spring and summer. This demarcation appears around 33-35°N in the middle of the plateau, and it is possibly associated with the high altitude terrain in the same geographic location. Comparisons of CALIPSO and MISR data show that the vertical dust occurrences are consistent with the spatial patterns of AOD. The different seasonal variation patterns between the northern and southern TP are primarily driven by atmospheric circulation, and are also related to the emission characteristics over the surrounding regions.

  9. Size Resolved Measurements of Springtime Aerosol Particles over the Northern South China Sea

    NASA Technical Reports Server (NTRS)

    Atwood, Samuel A.; Reid, Jeffrey S.; Kreidenweis, Sonia M.; Cliff, Stephen S.; Zhao, Yongjing; Lin, Neng-Huei; Tsay, Si-Chee; Chu, Yu-Chi; Westphal, Douglas L.

    2012-01-01

    Large sources of aerosol particles and their precursors are ubiquitous in East Asia. Such sources are known to impact the South China Sea (henceforth SCS), a sometimes heavily polluted region that has been suggested as particularly vulnerable to climate change. To help elucidate springtime aerosol transport into the SCS, an intensive study was performed on the remote Dongsha (aka Pratas) Islands Atoll in spring 2010. As part of this deployment, a Davis Rotating-drum Uniform size-cut Monitor (DRUM) cascade impactor was deployed to collect size-resolved aerosol samples at the surface that were analyzed by X-ray fluorescence for concentrations of selected elements. HYSPLIT backtrajectories indicated that the transport of aerosol observed at the surface at Dongsha was occurring primarily from regions generally to the north and east. This observation was consistent with the apparent persistence of pollution and dust aerosol, along with sea salt, in the ground-based dataset. In contrast to the sea-level observations, modeled aerosol transport suggested that the westerly flow aloft (w700 hPa) transported smoke-laden air toward the site from regions from the south and west. Measured aerosol optical depth at the site was highest during time periods of modeled heavy smoke loadings aloft. These periods did not coincide with elevated aerosol concentrations at the surface, although the model suggested sporadic mixing of this free-tropospheric aerosol to the surface over the SCS. A biomass burning signature was not clearly identified in the surface aerosol composition data, consistent with this aerosol type remaining primarily aloft and not mixing strongly to the surface during the study. Significant vertical wind shear in the region also supports the idea that different source regions lead to varying aerosol impacts in different vertical layers, and suggests the potential for considerable vertical inhomogeneity in the SCS aerosol environment.

  10. Recent Progress on Deep Blue Aerosol Algorithm as Applied TO MODIS, SEA WIFS, and VIIRS, and Their Intercomparisons with Ground Based and Other Satellite Measurements

    NASA Technical Reports Server (NTRS)

    Hsu, N. Christina; Bettenhausen, Corey; Sawyer, Andrew; Tsay, Si-Chee

    2012-01-01

    The impact of natural and anthropogenic sources of aerosols has gained increasing attention from scientific communities in recent years. Indeed, tropospheric aerosols not only perturb radiative energy balance by interacting with solar and terrestrial radiation, but also by changing cloud properties and lifetime. Furthermore, these anthropogenic and natural air particles, once generated over the source regions, can be transported out of the boundary layer into the free troposphere and can travel thousands of kilometers across oceans and continents resulting in important biogeochemical impacts on the ecosystem. With the launch of SeaWiFS in 1997, Terra/MODIS in 1999, and Aqua/MODIS in 2002, high quality comprehensive aerosol climatology is becoming feasible for the first time. As a result of these unprecedented data records, studies of the radiative and biogeochemical effects due to tropospheric aerosols are now possible. In this talk, we will demonstrate how this newly available SeaWiFS/MODIS aerosol climatology can provide an important piece of puzzles in reducing the uncertainty of estimated climatic forcing due to aerosols. We will start with the global distribution of aerosol loading and their variabilities over both land and ocean on short- and long-term temporal scales observed over the last decade. The recent progress made in Deep Blue aerosol algorithm on improving accuracy of these Sea WiFS / MODIS aerosol products in particular over land will be discussed. The impacts on quantifying physical and optical processes of aerosols over source regions of adding the Deep Blue products of aerosol properties over bright-reflecting surfaces into Sea WiFS / MODIS as well as VIIRS data suite will also be addressed. We will also show the intercomparison results of SeaWiFS/MODIS retrieved aerosol optical thickness with data from ground based AERONET sunphotometers over land and ocean as well as with other satellite measurements. The trends observed in global aerosol

  11. Aerosols and past environments: A global investigation into cave aerosol identification, distribution, and contribution to speleothem geochemistry

    NASA Astrophysics Data System (ADS)

    Dredge, J. A.; Fairchild, I. J.; Harrison, R. M.; Woodhead, J. D.; Hellstrom, J.; Mattey, D.

    2013-12-01

    A new sector of interest is developing within cave science regarding the influence of aerosols on the cave environment and the potential speleothem palaeoenvironmental aerosol record which may be preserved. This paper presents the results from a global collaboration project which explored all aspects of aerosols in the cave environment. Cave aerosol identification, introduction and distribution Cave aerosol multivariable environmental monitoring projects were carried out in the UK, Spain, Austria and Australia. Results demonstrate that cave ventilation is the predominant control on the introduction and distribution of aerosols throughout the cave environment (Dredge et al., 2013). Consequently, aerosol transportation processes vary as a result of seasonal ventilation changes and cave morphological features. Cave aerosol contribution to speleothem geochemistry Aerosol contributions to speleothem geochemistry were determined by comparing monitored aerosol deposition to speleothem trace element data. Significant aerosol contribution scenarios were identified as: hiatus events, high aerosol flux situations and secondary microbial concentration processes. Modelling indicates that a >99.9% reduction in drip water flow rates is required to reduce trace element supply quantities to equal that of aerosol supply (Dredge et al., 2013). Aerosol palaeoclimate and palaeoenvironmental records Aerosol contributions and the ability to utilise aerosol records in speleothem are investigated in samples from Gibraltar and Australia. Long range dust sources and past atmospheric circulation over several glacial cycles is studied through Sr isotope analysis of a Flowstone core from Gibraltar. Results of organic fire proxy analysis from Australian speleothem samples indicate an aerosol deposition forest fire record. In addition to primary fire deposition, secondary biological feedbacks and subsequent bioaccumulation processes in the cave environment are explored by microbial analysis

  12. Aerosol number size distributions over a coastal semi urban location: Seasonal changes and ultrafine particle bursts.

    PubMed

    Babu, S Suresh; Kompalli, Sobhan Kumar; Moorthy, K Krishna

    2016-09-01

    Number-size distribution is one of the important microphysical properties of atmospheric aerosols that influence aerosol life cycle, aerosol-radiation interaction as well as aerosol-cloud interactions. Making use of one-yearlong measurements of aerosol particle number-size distributions (PNSD) over a broad size spectrum (~15-15,000nm) from a tropical coastal semi-urban location-Trivandrum (Thiruvananthapuram), the size characteristics, their seasonality and response to mesoscale and synoptic scale meteorology are examined. While the accumulation mode contributed mostly to the annual mean concentration, ultrafine particles (having diameter <100nm) contributed as much as 45% to the total concentration, and thus constitute a strong reservoir, that would add to the larger particles through size transformation. The size distributions were, in general, bimodal with well-defined modes in the accumulation and coarse regimes, with mode diameters lying in the range 141 to 167nm and 1150 to 1760nm respectively, in different seasons. Despite the contribution of the coarse sized particles to the total number concentration being meager, they contributed significantly to the surface area and volume, especially during transport of marine air mass highlighting the role of synoptic air mass changes. Significant diurnal variation occurred in the number concentrations, geometric mean diameters, which is mostly attributed to the dynamics of the local coastal atmospheric boundary layer and the effect of mesoscale land/sea breeze circulation. Bursts of ultrafine particles (UFP) occurred quite frequently, apparently during periods of land-sea breeze transitions, caused by the strong mixing of precursor-rich urban air mass with the cleaner marine air mass; the resulting turbulence along with boundary layer dynamics aiding the nucleation. These ex-situ particles were observed at the surface due to the transport associated with boundary layer dynamics. The particle growth rates from

  13. Aerosol number size distributions over a coastal semi urban location: Seasonal changes and ultrafine particle bursts.

    PubMed

    Babu, S Suresh; Kompalli, Sobhan Kumar; Moorthy, K Krishna

    2016-09-01

    Number-size distribution is one of the important microphysical properties of atmospheric aerosols that influence aerosol life cycle, aerosol-radiation interaction as well as aerosol-cloud interactions. Making use of one-yearlong measurements of aerosol particle number-size distributions (PNSD) over a broad size spectrum (~15-15,000nm) from a tropical coastal semi-urban location-Trivandrum (Thiruvananthapuram), the size characteristics, their seasonality and response to mesoscale and synoptic scale meteorology are examined. While the accumulation mode contributed mostly to the annual mean concentration, ultrafine particles (having diameter <100nm) contributed as much as 45% to the total concentration, and thus constitute a strong reservoir, that would add to the larger particles through size transformation. The size distributions were, in general, bimodal with well-defined modes in the accumulation and coarse regimes, with mode diameters lying in the range 141 to 167nm and 1150 to 1760nm respectively, in different seasons. Despite the contribution of the coarse sized particles to the total number concentration being meager, they contributed significantly to the surface area and volume, especially during transport of marine air mass highlighting the role of synoptic air mass changes. Significant diurnal variation occurred in the number concentrations, geometric mean diameters, which is mostly attributed to the dynamics of the local coastal atmospheric boundary layer and the effect of mesoscale land/sea breeze circulation. Bursts of ultrafine particles (UFP) occurred quite frequently, apparently during periods of land-sea breeze transitions, caused by the strong mixing of precursor-rich urban air mass with the cleaner marine air mass; the resulting turbulence along with boundary layer dynamics aiding the nucleation. These ex-situ particles were observed at the surface due to the transport associated with boundary layer dynamics. The particle growth rates from

  14. Direct aerosol chemical composition measurements to evaluate the physicochemical differences between controlled sea spray aerosol generation schemes

    NASA Astrophysics Data System (ADS)

    Collins, D. B.; Zhao, D. F.; Ruppel, M. J.; Laskina, O.; Grandquist, J. R.; Modini, R. L.; Stokes, M. D.; Russell, L. M.; Bertram, T. H.; Grassian, V. H.; Deane, G. B.; Prather, K. A.

    2014-07-01

    Controlled laboratory studies of the physical and chemical properties of sea spray aerosol (SSA) must be underpinned by a physically and chemically accurate representation of the bubble mediated production of nascent SSA particles. Since bubble bursting is sensitive to the physicochemical properties of seawater, any important differences in the SSA production mechanism are projected into SSA composition. Using direct chemical measurements of SSA at the single-particle level, this study presents an inter-comparison of three laboratory-based, bubble-mediated SSA production schemes: gas forced through submerged sintered glass filters ("frits"), a pulsed plunging waterfall apparatus, and breaking waves in a wave channel filled with natural seawater. The size-resolved chemical composition of SSA particles produced by breaking waves is more similar to particles produced by the plunging waterfall than sintered glass filters. Aerosol generated by disintegrating foam produced by sintered glass filters contained a larger fraction of organic enriched particles and a different size-resolved elemental composition, especially in the 0.8-2 μm size range. These particles, when dried, had more spherical morphologies compared to the more cubic structure expected for pure NaCl particles, which can be attributed to the presence of additional organic carbon. In addition to an inter-comparison of three SSA production methods, the role of the episodic or "pulsed" nature of the waterfall method utilized in this study on SSA composition was undertaken. In organic-enriched seawater, the continuous operation of the plunging waterfall mechanism resulted in the accumulation of surface foam and an over-expression of organic matter in SSA particles compared to pulsed plunging waterfall. Throughout this set of experiments, comparative differences in the SSA number size distribution were coincident with differences in aerosol composition, indicating that the production mechanism of SSA exerts

  15. 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.; Ault, A.; Bondy, A.; Takahama, S.; Modini, R. L.; Baumann, K.; Edgerton, E.; Knote, C.; et al

    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

  16. Large-Scale Covariability Between Aerosol and Precipitation Over the 7-SEAS Region: Observations and Simulations

    NASA Technical Reports Server (NTRS)

    Huang, Jingfeng; Hsu, N. Christina; Tsay, Si-Chee; Zhang, Chidong; Jeong, Myeong Jae; Gautam, Ritesh; Bettenhausen, Corey; Sayer, Andrew M.; Hansell, Richard A.; Liu, Xiaohong; Jiang, Jonathan H.

    2012-01-01

    One of the seven scientific areas of interests of the 7-SEAS field campaign is to evaluate the impact of aerosol on cloud and precipitation (http://7-seas.gsfc.nasa.gov). However, large-scale covariability between aerosol, cloud and precipitation is complicated not only by ambient environment and a variety of aerosol effects, but also by effects from rain washout and climate factors. This study characterizes large-scale aerosol-cloud-precipitation covariability through synergy of long-term multi ]sensor satellite observations with model simulations over the 7-SEAS region [10S-30N, 95E-130E]. Results show that climate factors such as ENSO significantly modulate aerosol and precipitation over the region simultaneously. After removal of climate factor effects, aerosol and precipitation are significantly anti-correlated over the southern part of the region, where high aerosols loading is associated with overall reduced total precipitation with intensified rain rates and decreased rain frequency, decreased tropospheric latent heating, suppressed cloud top height and increased outgoing longwave radiation, enhanced clear-sky shortwave TOA flux but reduced all-sky shortwave TOA flux in deep convective regimes; but such covariability becomes less notable over the northern counterpart of the region where low ]level stratus are found. Using CO as a proxy of biomass burning aerosols to minimize the washout effect, large-scale covariability between CO and precipitation was also investigated and similar large-scale covariability observed. Model simulations with NCAR CAM5 were found to show similar effects to observations in the spatio-temporal patterns. Results from both observations and simulations are valuable for improving our understanding of this region's meteorological system and the roles of aerosol within it. Key words: aerosol; precipitation; large-scale covariability; aerosol effects; washout; climate factors; 7- SEAS; CO; CAM5

  17. Three optical methods for remotely measuring aerosol size distributions.

    NASA Technical Reports Server (NTRS)

    Reagan, J. A.; Herman, B. M.

    1971-01-01

    Three optical probing methods for remotely measuring atmospheric aerosol size distributions are discussed and contrasted. The particular detection methods which are considered make use of monostatic lidar (laser radar), bistatic lidar, and solar radiometer sensing techniques. The theory of each of these measurement techniques is discussed briefly, and the necessary constraints which must be applied to obtain aerosol size distribution information from such measurements are pointed out. Theoretical and/or experimental results are also presented which demonstrate the utility of the three proposed probing methods.

  18. 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

  19. Linking variations in sea spray aerosol particle hygroscopicity to composition during two microcosm experiments

    NASA Astrophysics Data System (ADS)

    Forestieri, Sara D.; Cornwell, Gavin C.; Helgestad, Taylor M.; Moore, Kathryn A.; Lee, Christopher; Novak, Gordon A.; Sultana, Camille M.; Wang, Xiaofei; Bertram, Timothy H.; Prather, Kimberly A.; Cappa, Christopher D.

    2016-07-01

    The extent to which water uptake influences the light scattering ability of marine sea spray aerosol (SSA) particles depends critically on SSA chemical composition. The organic fraction of SSA can increase during phytoplankton blooms, decreasing the salt content and therefore the hygroscopicity of the particles. In this study, subsaturated hygroscopic growth factors at 85 % relative humidity (GF(85 %)) of predominately submicron SSA particles were quantified during two induced phytoplankton blooms in marine aerosol reference tanks (MARTs). One MART was illuminated with fluorescent lights and the other was illuminated with sunlight, referred to as the "indoor" and "outdoor" MARTs, respectively. Optically weighted GF(85 %) values for SSA particles were derived from measurements of light scattering and particle size distributions. The mean optically weighted SSA diameters were 530 and 570 nm for the indoor and outdoor MARTs, respectively. The GF(85 %) measurements were made concurrently with online particle composition measurements, including bulk composition (using an Aerodyne high-resolution aerosol mass spectrometer) and single particle (using an aerosol time-of-flight mass spectrometer) measurement, and a variety of water-composition measurements. During both microcosm experiments, the observed optically weighted GF(85 %) values were depressed substantially relative to pure inorganic sea salt by 5 to 15 %. There was also a time lag between GF(85 %) depression and the peak chlorophyll a (Chl a) concentrations by either 1 (indoor MART) or 3-to-6 (outdoor MART) days. The fraction of organic matter in the SSA particles generally increased after the Chl a peaked, also with a time lag, and ranged from about 0.25 to 0.5 by volume. The observed depression in the GF(85 %) values (relative to pure sea salt) is consistent with the large observed volume fractions of non-refractory organic matter (NR-OM) comprising the SSA. The GF(85 %) values exhibited a reasonable negative

  20. Aerosol-cloud-land surface interactions within tropical sea breeze convection

    NASA Astrophysics Data System (ADS)

    Grant, Leah D.; Heever, Susan C.

    2014-07-01

    In this study, the influence of aerosols, surface roughness length, soil moisture, and synergistic interactions among these factors on tropical convective rainfall focused along a sea breeze front are explored within idealized cloud-resolving modeling simulations using the Regional Atmospheric Modeling System (RAMS). The idealized RAMS domain setup is representative of the coastal Cameroon rainforest in equatorial Africa. In order to assess the potential sensitivity of sea breeze convection to increasing anthropogenic activity and deforestation occurring in such regions, 27 total simulations are performed in which combinations of enhanced aerosol concentrations, reduced surface roughness length, and reduced soil moisture are included. Both enhanced aerosols and reduced soil moisture are found to individually reduce the precipitation due to reductions in downwelling shortwave radiation and surface latent heat fluxes, respectively, while perturbations to the roughness length do not have a large impact on the precipitation. The largest soil moisture perturbations dominate the precipitation changes due to reduced low-level moisture available to the convection, but if the soil moisture perturbation is more moderate, synergistic interactions between soil moisture and aerosols enhance the sea breeze precipitation. This is found to result from evening convection that forms ahead of the sea breeze only when both effects are present. Interactions between the resulting gust fronts and the sea breeze front locally enhance convergence and therefore the rainfall. The results of this study underscore the importance of considering the aerosol-cloud-land surface system responses to perturbations in aerosol loading and land surface characteristics.

  1. Aerosol size distribution, composition, and CO2 backscatter

    NASA Astrophysics Data System (ADS)

    Clarke, Antony D.; Porter, John N.

    1991-03-01

    The aerosol size distribution, composition, and CO2 backscatter at 10.6 microns (beta-CO2) were measured continuosly at the Mauna Loa Observatory (Hawaii) during January-March and November-December, 1988 periods to compare the characteristics of periods associated with appreciable Asian dust transport to that site (January-March) with those of periods characterized by low-dust condition. The aerosol size distribution in the range 0.15 micron to 7.6 microns was measured at temperatures of 40, 150, and 340 C to differentiate between volatile and nonvolatile aerosols. Large ranges of variability was found in measurements of aerosol size distribution during both periods, but the average distributions were similar for both the high-dust and the low-dust periods. However, values for beta-CO2 were more elevated (by about six times) during periods associated with active Asian dust transport to the observatory site than during the low-dust periods.

  2. Origin, Transport, and Vertical Distribution of Atmospheric Polluntants over the Northern Sourth China Sea During the 7-SEAS-Dongsha Experiment

    NASA Technical Reports Server (NTRS)

    Wang, Sheng-Hsiang; Tsay, Si-Chee; Lin, Neng-Huei; Chang, Shuenn-Chin; Li, Can; Welton, Ellsworth J.; Holben, Brent N.; Hsu, N. Christina; Lau, William K. M.; Lolli, Simone; Kuo, Chun-Chiang; Chia, Hao-Ping; Chia-Yang, Chiu; Chia-Ching, Lin; Bell, Shaun W.; Ji, Qiang; Hansell, Richard A.; Sheu, Guey-Rong; Chi, Kai-Hsien; Peng, Chi-Ming

    2012-01-01

    During the spring of 2010, comprehensive in situ measurements were made for the first time on a small atoll (Dongsha Island) in the northern South China Sea (SCS), a key region of the 7-SEAS (the Seven South East Asian Studies) program. This paper focuses on characterizing the source origins, transport processes, and vertical distributions of the Asian continental outflows over the region, using measurements including mass concentration, optical properties, hygroscopicity, and vertical distribution of the aerosol particles, as well as the trace gas composition. Cluster analysis of backward trajectories classified 52% of the air masses arriving at ground level of Dongsha Island as having a continental origin, mainly from northern China to the northern SCS, passing the coastal area and being confined in the marine boundary layer (0-0.5 km). Compared to aerosols of oceanic origin, the fine mode continental aerosols have a higher concentration, extinction coefficient, and single-scattering albedo at 550 nm (i.e., 19 vs. 14 microg per cubic meter in PM(sub 2.5); 77 vs. 59 M per meter in beta(sub e); and 0.94 vs. 0.90 in omega, respectively). These aerosols have a higher hygroscopicity (f at 85% RH = 2.1) than those in the upwind inland regions, suggesting that the aerosols transported to the northern SCS were modified by the marine environment. In addition to the near-surface aerosol transport, a significant upper-layer (3-4 km) transport of biomass-burning aerosols was observed. Our results suggest that emissions from both China and Southeast Asia could have a significant impact on the aerosol loading and other aerosol properties over the SCS. Furthermore, the complex vertical distribution of aerosols-coinciding-with-clouds has implications for remote-sensing observations and aerosol-cloud-radiation interactions.

  3. Controls on the distribution of deep-sea sediments

    NASA Astrophysics Data System (ADS)

    Dutkiewicz, A.; O'Callaghan, S.; Müller, R. D.

    2016-08-01

    Deep-sea sediments represent the largest geological deposit on Earth and provide a record of our planet's response to conditions at the sea surface from where the bulk of material originates. We use a machine learning method to analyze how the distribution of 14,400 deep-sea sediment sample lithologies is connected to bathymetry and surface oceanographic parameters. Our probabilistic Gaussian process classifier shows that the geographic occurrence of five major lithologies in the world's ocean can be predicted using just three parameters. Sea-surface salinity and temperature provide a major control for the growth and composition of plankton and specific ranges are also associated with the influx of non-aerosol terrigenous material into the ocean, while bathymetry is an important parameter for discriminating the occurrence of calcareous sediment, clay and coarse lithogenous sediment from each other. We find that calcareous and siliceous oozes are not linked to high surface productivity. Diatom and radiolarian oozes are associated with low salinities at the surface but with discrete ranges of temperatures, reflecting the diversity of planktonic species in different climatic zones. Biosiliceous sediments cannot be used to infer paleodepth, but are good indicators of paleotemperature and paleosalinity. Our analysis provides a new framework for constraining paleosurface ocean environments from the geological record of deep-sea sediments. It shows that small shifts in salinity and temperature significantly affect the lithology of seafloor sediment. As deep-sea sediments represent the largest carbon sink on Earth these shifts need to be considered in the context of global ocean warming.

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

    NASA Astrophysics Data System (ADS)

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

    2013-12-01

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

  5. Analysis of Organic Anionic Surfactants in Fine and Coarse Fractions of Freshly Emitted Sea Spray Aerosol.

    PubMed

    Cochran, Richard E; Laskina, Olga; Jayarathne, Thilina; Laskin, Alexander; Laskin, Julia; Lin, Peng; Sultana, Camille; Lee, Christopher; Moore, Kathryn A; Cappa, Christopher D; Bertram, Timothy H; Prather, Kimberly A; Grassian, Vicki H; Stone, Elizabeth A

    2016-03-01

    The inclusion of organic compounds in freshly emitted sea spray aerosol (SSA) has been shown to be size-dependent, with an increasing organic fraction in smaller particles. Here we have used electrospray ionization-high resolution mass spectrometry in negative ion mode to identify organic compounds in nascent sea spray collected throughout a 25 day mesocosm experiment. Over 280 organic compounds from ten major homologous series were tentatively identified, including saturated (C8-C24) and unsaturated (C12-C22) fatty acids, fatty acid derivatives (including saturated oxo-fatty acids (C5-C18) and saturated hydroxy-fatty acids (C5-C18), organosulfates (C2-C7, C12-C17) and sulfonates (C16-C22). During the mesocosm, the distributions of molecules within some homologous series responded to variations among the levels of phytoplankton and bacteria in the seawater. The average molecular weight and carbon preference index of saturated fatty acids significantly decreased within fine SSA during the progression of the mesocosm, which was not observed in coarse SSA, sea-surface microlayer or in fresh seawater. This study helps to define the molecular composition of nascent SSA and biological processes in the ocean relate to SSA composition. PMID:26828238

  6. Combined X-Ray and Raman Spectroscopic Techniques for the Characterization of Sea Spray Aerosol

    NASA Astrophysics Data System (ADS)

    Aller, J. Y.; Alpert, P. A.; Knopf, D. A.; Kilthau, W.; Bothe, D.; Charnawskas, J. C.; Gilles, M. K.; OBrien, R. E.; Moffet, R.; Radway, J.

    2014-12-01

    Sea spray aerosol along with mineral dust dominates the global mass flux of particles to the atmosphere. Marine aerosol particles are of particular interest because of their continual impact on cloud formation, precipitation, atmospheric chemical processes, and thus global climate. Here we report on the physical/chemical characteristics of sub-surface waters, aerosolized sea spray particles, and particles/organic species present in surface microlayer (SML) samples collected during oceanic field campaigns and generated during laboratory experiments, revealing a biogenic primary source of the organic fraction of airborne particles. We also report on ice nucleation experiments with aerosolized particles collected during the May 2014 WACS II North Atlantic cruise and with laboratory generated exudate material from diatom cultures with the potential to impact cirrus and mixed phase clouds. Physicochemical analyses using a multi-modal approach which includes Scanning Transmission X-ray Microscopy coupled with Near-Edge Absorption Fine Structure Spectroscopy (STXM/NEXAFS) and Raman spectroscopy confirm the presence and chemical similarity of polysaccharide-rich transparent exopolymer (TEP) material and proteins in both SML sea spray aerosol and ice forming aerosol particles, regardless of the extent of biological activity in surface waters. Our results demonstrate a direct relationship between the marine environment and composition of marine aerosol through primary particle emission.

  7. VARIATIONS OF MERIDIONAL AEROSOL DISTRIBUTION AND SOLAR DIMMING

    SciTech Connect

    Kishcha, P.; Starobinets, B.; Kalashnikova, O.; Long, Charles N.; Alpert, P.

    2009-06-08

    Meridional distribution of aerosol optical thickness (AOT) over the ocean was analyzed by using the eight-year MISR and MODIS-Terra data sets, from March 2000 to February 2008, as well as the five-year MODIS-Aqua data set, from July 2002 to June 2007. The three independent sensors show that there was a pronounced meridional aerosol asymmetry. It was found that there were strong seasonal variations in the hemispheric aerosol asymmetry: it was pronounced during the half-year period, from March to August (the most pronounced asymmetry was observed from April to July). There was no noticeable asymmetry during the season from September to December. Not only has the Northern hemisphere, where the main sources of aerosols are located, but also the Southern hemisphere contributed to the formation of noticeable aerosol asymmetry. The increase in AOT, averaged over the Northern hemisphere during the season of pronounced hemispheric aerosol asymmetry, was accompanied by a decrease in AOT, averaged over the Southern hemisphere. In both hemispheres, amplitudes of seasonal AOT variations decreases from mid-latitudes (60N - 30N and 30S - 60S) to low latitudes (30N - 0 and 0 - 30S) respectively, indicating that the contribution of AOT averaged over mid-latitudes to the formation of pronounced meridional hemispheric asymmetry and its seasonal variations is more significant than the contribution of AOT averaged over low latitudes. For the season of prominent hemispheric aerosol asymmetry, from April to July, during the eight-year period under consideration, a declining long-term tendency of AOT prevailed at latitudes between 30oN and 60oN, suggesting brightening over the cloud-free ocean.

  8. Modal structure of chemical mass size distribution in the high Arctic aerosol

    NASA Astrophysics Data System (ADS)

    Hillamo, Risto; Kerminen, Veli-Matti; Aurela, Minna; MäKelä, Timo; Maenhaut, Willy; Leek, Caroline

    2001-11-01

    Chemical mass size distributions of aerosol particles were measured in the remote marine boundary layer over the central Arctic Ocean as part of the Atmospheric Research Program on the Arctic Ocean Expedition 1996 (AOE-96). An inertial impaction method was used to classify aerosol particles into different size classes for subsequent chemical analysis. The particle chemical composition was determined by ion chromatography and by the particle-induced X-ray emission technique. Continuous particle size spectra were extracted from the raw data using a data inversion method. Clear and varying modal structures for aerosols consisting of primary sea-salt particles or of secondary particles related to dimethyl sulfide emissions were found. Concentration levels of all modes decreased rapidly when the distance from open sea increased. In the submicrometer size range the major ions found by ion chromatography were sulfate, methane sulfonate, and ammonium. They had most of the time a clear Aitken mode and one or two accumulation modes, with aerodynamic mass median diameters around 0.1 μm, 0.3 μm, and between 0.5-1.0 μm, respectively. The overall submicron size distributions of these three ions were quite similar, suggesting that they were internally mixed over most of this size range. The corresponding modal structure was consistent with the mass size distributions derived from the particle number size distributions measured with a differential mobility particle sizer. The Aitken to accumulation mode mass ratio for nss-sulfate and MSA was substantially higher during clear skies than during cloudy periods. Primary sea-salt particles formed a mode with an aerodynamic mass median diameter around 2 μm. In general, the resulting continuous mass size distributions displayed a clear modal structure consistent with our understanding of the two known major source mechanisms. One is the sea-salt aerosol emerging from seawater by bubble bursting. The other is related to

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

    NASA Technical Reports Server (NTRS)

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

    1989-01-01

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

  10. Global and Regional Evaluation of Over-Land Spectral Aerosol Optical Depth Retrievals from SeaWiFS

    NASA Technical Reports Server (NTRS)

    Sayer, A. M.; Hsu, N. C.; Bettenhausen, C.; Jeong, M. J.; Holben, B. N.; Zhang, J.

    2012-01-01

    This study evaluates a new spectral aerosol optical depth (AOD) dataset derived from Sea-viewing Wide Field-of-view Sensor (Sea WiFS) measurements over land. First, the data are validated against Aerosol Robotic Network (AERONET) direct-sun AOD measurements, and found to compare well on a global basis. If only data with the highest quality flag are used, the correlation is 0.86 and 72% of matchups fall within an expected absolute uncertainty of 0.05 + 20% (for the wavelength of 550 nm). The quality is similar at other wavelengths and stable over the 13-year (1997-2010) mission length. Performance tends to be better over vegetated, low-lying terrain with typical AOD of 0.3 or less, such as found over much of North America and Eurasia. Performance tends to be poorer for low-AOD conditions near backscattering geometries, where Sea WiFS overestimates AOD, or optically-thick cases of absorbing aerosol, where SeaWiFS tends to underestimate AOD. Second, the SeaWiFS data are compared with midvisible AOD derived from the Moderate Resolution Imaging Spectrometer (MODIS) and Multiangle Imaging Spectroradiometer (MISR). All instruments show similar spatial and seasonal distributions of AOD, although there are regional and seasonal offsets between them. At locations where AERONET data are available, these offsets are largely consistent with the known validation characteristics of each dataset. With the results of this study in mind, the SeaWiFS over-land AOD record should be suitable for quantitative scientific use.

  11. The Sensitivity of SeaWiFS Ocean Color Retrievals to Aerosol Amount and Type

    NASA Technical Reports Server (NTRS)

    Kahn, Ralph A.; Sayer, Andrew M.; Ahmad, Ziauddin; Franz, Bryan A.

    2016-01-01

    As atmospheric reflectance dominates top-of-the-atmosphere radiance over ocean, atmospheric correction is a critical component of ocean color retrievals. This paper explores the operational Sea-viewing Wide Field-of-View Sensor (SeaWiFS) algorithm atmospheric correction with approximately 13 000 coincident surface-based aerosol measurements. Aerosol optical depth at 440 nm (AOD(sub 440)) is overestimated for AOD below approximately 0.1-0.15 and is increasingly underestimated at higher AOD; also, single-scattering albedo (SSA) appears overestimated when the actual value less than approximately 0.96.AOD(sub 440) and its spectral slope tend to be overestimated preferentially for coarse-mode particles. Sensitivity analysis shows that changes in these factors lead to systematic differences in derived ocean water-leaving reflectance (Rrs) at 440 nm. The standard SeaWiFS algorithm compensates for AOD anomalies in the presence of nonabsorbing, medium-size-dominated aerosols. However, at low AOD and with absorbing aerosols, in situ observations and previous case studies demonstrate that retrieved Rrs is sensitive to spectral AOD and possibly also SSA anomalies. Stratifying the dataset by aerosol-type proxies shows the dependence of the AOD anomaly and resulting Rrs patterns on aerosol type, though the correlation with the SSA anomaly is too subtle to be quantified with these data. Retrieved chlorophyll-a concentrations (Chl) are affected in a complex way by Rrs differences, and these effects occur preferentially at high and low Chl values. Absorbing aerosol effects are likely to be most important over biologically productive waters near coasts and along major aerosol transport pathways. These results suggest that future ocean color spacecraft missions aiming to cover the range of naturally occurring and anthropogenic aerosols, especially at wavelengths shorter than 440 nm, will require better aerosol amount and type constraints.

  12. Airborne Measurements of Aerosol Size Distributions During PACDEX

    NASA Astrophysics Data System (ADS)

    Rogers, D. C.; Gandrud, B.; Campos, T.; Kok, G.; Stith, J.

    2007-12-01

    The Pacific Dust Experiment (PACDEX) is an airborne project that attempts to characterize the indirect aerosol effect by tracing plumes of dust and pollution across the Pacific Ocean. This project occurred during April-May 2007 and used the NSF/NCAR HIAPER research aircraft. When a period of strong generation of dust particles and pollution was detected by ground-based and satellite sensors, then the aircraft was launched from Colorado to Alaska, Hawaii, and Japan. Its mission was to intercept and track these plumes from Asia, across the Pacific Ocean, and ultimately to the edges of North America. For more description, see the abstract by Stith and Ramanathan (this conference) and other companion papers on PACDEX. The HIAPER aircraft carried a wide variety of sensors for measuring aerosols, cloud particles, trace gases, and radiation. Sampling was made in several weather regimes, including clean "background" air, dust and pollution plumes, and regions with cloud systems. Altitude ranges extended from 100 m above the ocean to 13.4 km. This paper reports on aerosol measurements made with a new Ultra-High Sensitivity Aerosol Spectrometer (UHSAS), a Radial Differential Mobility Analyzer (RDMA), a water-based CN counter, and a Cloud Droplet Probe (CDP). These cover the size range 10 nm to 10 um diameter. In clear air, dust was detected with the UHSAS and CDP. Polluted air was identified with high concentrations of carbon monoxide, ozone, and CN. Aerosol size distributions will be presented, along with data to define the context of weather regimes.

  13. Anthropogenic influence on the distribution of tropospheric sulphate aerosol

    NASA Astrophysics Data System (ADS)

    Langner, J.; Rodhe, H.; Crutzen, P. J.; Zimmermann, P.

    1992-10-01

    HUMAN activities have increased global emissions of sulphur gases by about a factor of three during the past century, leading to increased sulphate aerosol concentrations, mainly in the Northern Hemisphere. Sulphate aerosols can affect the climate directly, by increasing the backscattering of solar radiation in cloud-free air, and indirectly, by providing additional cloud condensation nuclei1-4. Here we use a global transport-chemistry model to estimate the changes in the distribution of tropospheric sulphate aerosol and deposition of non-seasalt sulphur that have occurred since pre-industrial times. The increase in sulphate aerosol concentration is small over the Southern Hemisphere oceans, but reaches a factor of 100 over northern Europe in winter. Our calculations indicate, however, that at most 6% of the anthropogenic sulphur emissions is available for the formation of new aerosol particles. This is because about one-half of the sulphur dioxide is deposited on the Earth's surface, and most of the remainder is oxidized in cloud droplets so that the sulphate becomes associated with pre-existing particles. Even so, the rate of formation of new sulphate particles may have doubled since pre-industrial times.

  14. GNI - A System for the Impaction and Automated Optical Sizing of Giant Aerosol Particles with Emphasis on Sea Salt

    NASA Astrophysics Data System (ADS)

    Jensen, Jorgen

    2013-04-01

    Size distributions of giant aerosol particles (e.g. sea-salt particles, dry radius larger than 0.5 μm) are not well characterized in the atmosphere, yet they contribute greatly to both direct and indirect aerosol effects. Measurements are problematic for these particles because they (i) occur in low concentrations, (ii) have difficulty in passing through air inlets, (iii) there are problems in discriminating between dry and deliquesced particles, (iv) and impaction sampling requires labor intensive methods. In this study, a simple, high-volume impaction system called the Giant Nuclei Impactor (GNI), based on free-stream exposure of polycarbonate slides from aircraft is described, along with an automated optical microscope-based system for analysis of the impacted particles. The impaction slides are analyzed in a humidity-controlled box (typically 90% relative humidity) that allows for deliquescence of sea salt particles. A computer controlled optical microscope with two digital cameras is used to acquire and analyze images of the aerosol particles. Salt particles will form near-spherical cap solution drops at high relative humidity. The salt mass in each giant aerosol particle is then calculated using simple geometry and K ̈ohler theory by assuming a NaCl composition. The system has a sample volume of about 10 L/s at aircraft speeds of 105 m/s. For salt particles, the measurement range is from about 0.7 μm dry radius to tens of micrometers, with a size-bin resolution of 0.2 μm dry radius. The sizing accuracy was tested using glass beads of known size. Characterizing the uncertainties of observational data is critical for applications to atmospheric science studies. A comprehensive uncertainty analysis is performed for the airborne GNI manual impaction and automatic optical microscope system for sizing giant aerosol particles, with particular emphasis on sea-salt particles. The factors included are (i) sizing accuracy, (ii) concentration accuracy, (iii

  15. Arctic Sea Salt Aerosol from Blowing Snow and Sea Ice Surfaces - a Missing Natural Source in Winter

    NASA Astrophysics Data System (ADS)

    Frey, M. M.; Norris, S. J.; Brooks, I. M.; Nishimura, K.; Jones, A. E.

    2015-12-01

    Atmospheric particles in the polar regions consist mostly of sea salt aerosol (SSA). SSA plays an important role in regional climate change through influencing the surface energy balance either directly or indirectly via cloud formation. SSA irradiated by sunlight also releases very reactive halogen radicals, which control concentrations of ozone, a pollutant and greenhouse gas. However, models under-predict SSA concentrations in the Arctic during winter pointing to a missing source. It has been recently suggested that salty blowing snow above sea ice, which is evaporating, to be that source as it may produce more SSA than equivalent areas of open ocean. Participation in the 'Norwegian Young Sea Ice Cruise (N-ICE 2015)' on board the research vessel `Lance' allowed to test this hypothesis in the Arctic sea ice zone during winter. Measurements were carried out from the ship frozen into the pack ice North of 80º N during February to March 2015. Observations at ground level (0.1-2 m) and from the ship's crows nest (30 m) included number concentrations and size spectra of SSA (diameter range 0.3-10 μm) as well as snow particles (diameter range 50-500 μm). During and after blowing snow events significant SSA production was observed. In the aerosol and snow phase sulfate is fractionated with respect to sea water, which confirms sea ice surfaces and salty snow, and not the open ocean, to be the dominant source of airborne SSA. Aerosol shows depletion in bromide with respect to sea water, especially after sunrise, indicating photochemically driven release of bromine. We discuss the SSA source strength from blowing snow in light of environmental conditions (wind speed, atmospheric turbulence, temperature and snow salinity) and recommend improved model parameterisations to estimate regional aerosol production. N-ICE 2015 results are then compared to a similar study carried out previously in the Weddell Sea during the Antarctic winter.

  16. Solution of multifrequency lidar inverse problem for a pre-set marine aerosol size-distribution formula

    SciTech Connect

    Piskozub, J.

    1994-12-31

    The multifrequency lidar inverse problem discussed consists of calculating the size distribution of sol particles from backscattered lidar data. Sea-water (marine) aerosol is particularly well suited for this kind of study as its scattering characteristics can be accurately represented by Mie theory as its particles are almost spherical and their complex index of refraction is well known. Here, a solution of the inverse problem concerning finding aerosol size distribution for a multifrequency lidar system working on a small number of wavelengths is proposed. The solution involves a best-fit method of finding parameters in a pre-set formula of particle size distribution. A comparison of results calculated with the algorithm from experimental lidar profiles with PMS data collected in Baltic Sea coastal zone is given.

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

    NASA Astrophysics Data System (ADS)

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

    2014-11-01

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

  18. Spectroscopic investigations of organic aerosol and its reaction with halogens, released by sea-salt activation

    NASA Astrophysics Data System (ADS)

    Ofner, J.; Zetzsch, C.

    2009-04-01

    The release of reactive halogen species from sea-salt aerosol offers a class of reactants for heterogeneous reactions of utmost importance. These heterogeneous reactions have been overlooked so far, although they may occur with internal and external mixtures of sea-salt aerosol and organic aerosol or organic matter. Such reactions might constitute sources of gaseous organohalogen compounds or halogenated organic aerosol in the atmospheric boundary layer. Infrared and UV/VIS spectroscopy provide an insight into chemical processes at reactive sites of the organic phase on a molecular level. Model studies of heterogeneous reactions of halogens with different kinds of (secondary) organic aerosols and organic matter were performed using a 700L smog chamber with a solar simulator. The model compounds alpha-pinene, catechol and humic acid have been chosen as precursors/material for the condensed, organic phase of the aerosol. After formation of the secondary organic aerosol or preparation of the organic material and the sea-salt solution the reaction was carried out using molecular chlorine and bromine in the presence of simulated sunlight. Chemical transformation of the organic material was studied using attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR) on a ZnSe crystal and diffuse reflectance UV/VIS spectroscopy. An electrostatic precipitator was developed to deposit the aerosol particles on the ATR crystal as a thin film. On the other hand, longpath-FTIR spectroscopy with a 40m White-cell allows us to monitor both the condensed and gas phase of the aerosol in situ in the smog chamber directly. These spectroscopic techniques enable us to characterize different organic aerosol particles and their functional groups at reactive sites on these particles as well as to study aerosol formation and transformation directly. The heterogeneous reaction of reactive halogen species with organic material at atmospheric conditions leads to small reactive

  19. PARTICLE SIZE DISTRIBUTIONS FOR AN OFFICE AEROSOL

    EPA Science Inventory

    The article discusses an evaluation of the effect of percent outdoor air supplied and occupation level on the particle size distributions and mass concentrations for a typical office building. (NOTE: As attention has become focused on indoor air pollution control, it has become i...

  20. Aerosol vertical distribution over east China from RIEMS-Chem simulation in comparison with CALIPSO measurements

    NASA Astrophysics Data System (ADS)

    Li, Jiawei; Han, Zhiwei

    2016-10-01

    The horizontal and vertical distributions of aerosol extinction coefficient (AEC) and mass concentration over east China in October 2010 were investigated by using an online-coupled regional climate model and CALIPSO (Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observations) data. Model performance was evaluated comprehensively against ground observations of meteorological variables and PM10 concentrations and CALIPSO retrieved AEC profiles, which demonstrated a good ability of the model in simulating spatial distribution and evolution of aerosol concentration and optical properties. Severe pollution episodes were found over wide areas of east China during the study period, with the maximum mean PM10 concentration exceeding 200 μg m-3 in the Chongqing district and a part of the lower reaches of the Yellow River on 8-10 October. Both CALIPSO retrievals and model simulations revealed high AEC values (≥1 km-1) often occurred within 2 km above ground over most areas of east China. AEC vertical profile in or in the vicinity of China major cities along CALIPSO orbit track exhibited two typical features: one was AEC reached its maximum (∼4 km-1) near the surface (<200 m) and decreased rapidly to < 0.1 km-1 at altitudes above 1 km, another one was AEC peaked at higher altitudes of about 0.5-1 km with a maximum up to 3 km-1. AEC vertical profile was strongly dependent on vertical distribution of both aerosol concentration, composition and relative humidity. The vertical cross sections over typical regions of east China exhibited a decreasing AEC in magnitude from the continent to the China seas. Over the continent, AEC was either maximum near the surface or peaked at higher altitudes (0.5-1.0 km) due to increases of relative humidity or aerosol concentration in those regions, whereas over the seas of China, AEC profile was characterized by peak values at an altitude around 1 km, mainly due to an elevated relative humidity there, which favored rapid aerosol

  1. Characteristics of aerosol types during large-scale transport of air pollution over the Yellow Sea region and at Cheongwon, Korea, in 2008.

    PubMed

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

    2012-04-01

    Episodes of large-scale transport of airborne dust and anthropogenic pollutant particles from different sources in the East Asian continent in 2008 were identified by National Oceanic and Atmospheric Administration satellite RGB (red, green, and blue)-composite images and the mass concentrations of ground level particulate matter. These particles were divided into dust, sea salt, smoke plume, and sulfate by an aerosol classification algorithm. To analyze the aerosol size distribution during large-scale transport of atmospheric aerosols, aerosol optical depth (AOD) and fine aerosol weighting (FW) of moderate imaging spectroradiometer aerosol products were used over the East Asian region. Six episodes of massive airborne dust particles, originating from sandstorms in northern China, Mongolia, and the Loess Plateau of China, were observed at Cheongwon. Classified dust aerosol types were distributed on a large-scale over the Yellow Sea region. The average PM10 and PM2.5 ratio to the total mass concentration TSP were 70% and 15%, respectively. However, the mass concentration of PM2.5 among TSP increased to as high as 23% in an episode where dust traveled in by way of an industrial area in eastern China. In the other five episodes of anthropogenic pollutant particles that flowed into the Korean Peninsula from eastern China, the anthropogenic pollutant particles were largely detected in the form of smoke over the Yellow Sea region. The average PM10 and PM2.5 ratios to TSP were 82% and 65%, respectively. The ratio of PM2.5 mass concentrations among TSP varied significantly depending on the origin and pathway of the airborne dust particles. The average AOD for the large-scale transport of anthropogenic pollutant particles in the East Asian region was measured to be 0.42 ± 0.17, which is higher in terms of the rate against atmospheric aerosols as compared with the AOD (0.36 ± 0.13) for airborne dust particles with sandstorms. In particular, the region ranging from eastern

  2. 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, Hannah M.; Draper, Danielle C.; Ayres, Benjamin R.; Ault, Andrew P.; Bondy, Amy L.; Takahama, S.; Modini, Robert; Baumann, K.; Edgerton, Eric S.; Knote, Christoph; Laskin, Alexander; Wang, Bingbing; Fry, Juliane L.

    2015-09-25

    The 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 1 June to 15 July 2013 Southern Oxidant and Aerosol Study (SOAS) campaign. Measurements using a Monitor for AeRosols and GAses (MARGA), an ion chromatograph coupled with a wet rotating denuder and a steam-jet aerosol collector for monitoring of ambient inorganic gas and aerosol species, revealed two periods of high aerosol nitrate (NO3 ) concentrations during the campaign. These periods of high nitrate were correlated with increased concentrations of coarse mode mineral or sea spray aerosol species, particularly Na+ and Ca2+, and with a shift towards aerosol with larger (1 to 2.5 um) diameters. We suggest this nitrate aerosol forms by multiphase reactions of HNO3 and particles, reactions that are facilitated by transport of mineral 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. 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 dust 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.

  3. Aerosol Types using Passive Remote Sensing: Global Distribution, Consistency Check, Total-Column Investigation and Translation into Composition Derived from Climate and Chemical Transport Model

    NASA Astrophysics Data System (ADS)

    Kacenelenbogen, M. S.; Dawson, K. W.; Johnson, M. S.; Burton, S. P.; Redemann, J.; Hasekamp, O. P.; Hair, J. W.; Ferrare, R. A.; Butler, C. F.; Holben, B. N.; Beyersdorf, A. J.; Ziemba, L. D.; Froyd, K. D.; Dibb, J. E.; Shingler, T.; Sorooshian, A.; Jimenez, J. L.; Campuzano Jost, P.; Jacob, D. J.

    2015-12-01

    To improve the predictions of aerosol composition in chemical transport models (CTMs) and global climate models (GCMs), we have developed an aerosol classification algorithm (called Specified Clustering and Mahalanobis Classification, SCMC) that assigns an aerosol type to multi-parameter retrievals by spaceborne, airborne or ground based passive remote sensing instruments [Russell et al., 2014]. The aerosol types identified by our scheme are pure dust, polluted dust, urban-industrial/developed economy, urban-industrial/developing economy, dark biomass smoke, light biomass smoke and pure marine. We apply the SCMC method to two different total-column datasets of aerosol optical properties: inversions from the ground-based AErosol RObotic NETwork (AERONET) and retrievals from the space-borne POLDER (Polarization and Directionality of Earth's Reflectances) instrument. The POLDER retrievals that we use differ from the standard POLDER retrievals [Deuzé et al., 2001] as they make full use of multi-angle, multispectral polarimetric data [Hasekamp et al., 2011]. We analyze agreement in the aerosol types inferred from both AERONET and POLDER globally. Then, we investigate how our total-column "effective" SCMC aerosol types relate to different aerosol types within the column (i.e. either a mixture of different types within one layer in the vertical or the stacking of different aerosol types within the vertical column). For that, we compare AERONET-SCMC aerosol types to collocated NASA LaRC HSRL vertically resolved aerosol types [Burton et al., 2012] during the SEAC4RS and DISCOVER-AQ airborne field experiments, mostly over Texas in Aug-Sept 2013. Finally, in order to evaluate the GEOS-Chem CTM aerosol types, we translate each of our SCMC aerosol type into a unique distribution of GEOS-Chem aerosol composition (e.g. biomass burning, dust, sulfate, sea salt). We bridge the gap between remote sensing and model-inferred aerosol types by using multiple years of collocated AERONET

  4. Aerosol deposition favors red tide phytoplankton in the East China Sea

    NASA Astrophysics Data System (ADS)

    Mackey, K. R.; Chien, C.; Chen, Y.; Glover, D. M.; Paytan, A.

    2013-12-01

    Chinese marginal seas support vast fisheries and vital economies, but their productivity is threatened by eutrophication from runoff and atmospheric deposition. The East China Sea is inundated with nitrogen from the Yangtze River and anthropogenic emissions, leading to elevated N:P ratios. We show that aerosol additions approximating one week of moderate deposition to offshore waters favor the growth of red tide phytoplankton, such as Skeletonema costatum, by providing nutrients and trace metals (iron and zinc) needed for growth. In contrast toxin-producing Pseudonitzchia does not benefit from aerosols in this region, possibly due to its preference for lower N:P ratios. A dose-dependent toxic response was observed in Synechococcus at high aerosol loads approximating a week of heavy deposition in the region. In contrast, phytoplankton growth at an onshore station was light limited, and aerosol additions did not have an appreciable effect on phytoplankton growth. Aerosol and chlorophyll observations from the Moderate Resolution Imaging Spectroradiometer (MODIS) satellite have the potential to explore the effect of aerosols on phytoplankton blooms over longer time scales and seasons. This study shows the potential for aerosols to control N:P ratios in offshore waters and to shape the phytoplankton community through fertilization and toxicity, contributing to the occurrence of red tides.

  5. Mass size distributions of elemental aerosols in industrial area

    PubMed Central

    Moustafa, Mona; Mohamed, Amer; Ahmed, Abdel-Rahman; Nazmy, Hyam

    2014-01-01

    Outdoor aerosol particles were characterized in industrial area of Samalut city (El-minia/Egypt) using low pressure Berner cascade impactor as an aerosol sampler. The impactor operates at 1.7 m3/h flow rate. Seven elements were investigated including Ca, Ba, Fe, K, Cu, Mn and Pb using atomic absorption technique. The mean mass concentrations of the elements ranged from 0.42 ng/m3 (for Ba) to 89.62 ng/m3 (for Fe). The mass size distributions of the investigated elements were bi-modal log normal distribution corresponding to the accumulation and coarse modes. The enrichment factors of elements indicate that Ca, Ba, Fe, K, Cu and Mn are mainly emitted into the atmosphere from soil sources while Pb is mostly due to anthropogenic sources. PMID:26644919

  6. New Aerosol Models for the Retrieval of Aerosol Optical Thickness and Normalized Water-Leaving Radiances from the SeaWiFS and MODIS Sensors Over Coastal Regions and Open Oceans

    NASA Technical Reports Server (NTRS)

    Ahmad, Ziauddin; Franz, Bryan A.; McClain, Charles R.; Kwiatkowska, Ewa J.; Werdell, Jeremy; Shettle, Eric P.; Holben, Brent N.

    2010-01-01

    We describe the development of a new suite of aerosol models for the retrieval of atmospheric and oceanic optical properties from the SeaWiFs and MODIS sensors, including aerosol optical thickness (tau), angstrom coefficient (alpha), and water-leaving radiance (L(sub w)). The new aerosol models are derived from Aerosol Robotic Network (AERONET) observations and have bimodal lognormal distributions that are narrower than previous models used by the Ocean Biology Processing Group. We analyzed AERONET data over open ocean and coastal regions and found that the seasonal variability in the modal radii, particularly in the coastal region, was related to the relative humidity, These findings were incorporated into the models by making the modal radii, as well as the refractive indices, explicitly dependent on relative humidity, From those findings, we constructed a new suite of aerosol models. We considered eight relative humidity values (30%, 50%, 70%, 75%, 80%, 85%, 90%. and 95%) and, for each relative humidity value, we constructed ten distributions by varying the fine-mode fraction from zero to 1. In all. 80 distributions (8Rh x 10 fine-mode fractions) were created to process the satellite data. We. also assumed that the coarse-mode particles were nonabsorbing (sea salt) and that all observed absorptions were entirely due to fine-mode particles. The composition of fine mode was varied to ensure that the new models exhibited the same spectral dependence of single scattering albedo as observed in the AERONET data,

  7. Characterization of aerosol episodes in the greater Mediterranean Sea area from satellite observations (2000-2007)

    NASA Astrophysics Data System (ADS)

    Gkikas, A.; Hatzianastassiou, N.; Mihalopoulos, N.; Torres, O.

    2016-03-01

    An algorithm able to identify and characterize episodes of different aerosol types above sea surfaces of the greater Mediterranean basin (GMB), including the Black Sea and the Atlantic Ocean off the coasts of Iberia and northwest Africa, is presented in this study. Based on this algorithm, five types of intense (strong and extreme) aerosol episodes in the GMB are identified and characterized using daily aerosol optical properties from satellite measurements, namely MODIS-Terra, Earth Probe (EP)-TOMS and OMI-Aura. These aerosol episodes are: (i) biomass-burning/urban-industrial (BU), (ii) desert dust (DD), (iii) dust/sea-salt (DSS), (iv) mixed (MX) and (v) undetermined (UN). The identification and characterization is made with our algorithm using a variety of aerosol properties, namely aerosol optical depth (AOD), Ångström exponent (α), fine fraction (FF), effective radius (reff) and Aerosol Index (AI). During the study period (2000-2007), the most frequent aerosol episodes are DD, observed primarily in the western and central Mediterranean Sea, and off the northern African coasts, 7 times/year for strong episodes and 4 times/year for extreme ones, on average. The DD episodes yield 40% of all types of strong aerosol episodes in the study region, while they account for 71.5% of all extreme episodes. The frequency of occurrence of strong episodes exhibits specific geographical patterns, for example the BU are mostly observed along the coasts of southern Europe and off the Atlantic coasts of Portugal, the MX episodes off the Spanish Mediterranean coast and over the Adriatic and northern Aegean Sea, while the DSS ones over the western and central Mediterranean Sea. On the other hand, the extreme episodes for all but DD aerosol display more patchy spatial patterns. The strong episodes exhibit AOD at 550 nm as high as 1.6 in the southernmost parts of central and eastern Mediterranean Sea, which rise up to 5 for the extreme, mainly DD and DSS, episodes. Although more

  8. Assessment of microphysical and chemical factors of aerosols over seas of the Russian Artic Eastern Section

    NASA Astrophysics Data System (ADS)

    Golobokova, Liudmila; Polkin, Victor

    2014-05-01

    The newly observed kickoff of the Northern Route development drew serious attention to state of the Arctic Resource environment. Occurring climatic and environmental changes are more sensitively seen in polar areas in particular. Air environment control allows for making prognostic assessments which are required for planning hazardous environmental impacts preventive actions. In August - September 2013, RV «Professor Khlustin» Northern Sea Route expeditionary voyage took place. En-route aerosol sampling was done over the surface of the Beringov, Chukotka and Eastern-Siberia seas (till the town of Pevek). The purpose of sampling was to assess spatio-temporal variability of optic, microphysical and chemical characteristics of aerosol particles of the surface layer within different areas adjacent to the Northern Sea Route. Aerosol test made use of automated mobile unit consisting of photoelectric particles counter AZ-10, aetalometr MDA-02, aspirator on NBM-1.2 pump chassis, and the impactor. This set of equipment allows for doing measurements of number concentration, dispersed composition of aerosols within sizes d=0.3-10 mkm, mass concentration of submicron sized aerosol, and filter-conveyed aerosols sampling. Filter-conveyed aerosols sampling was done using method accepted by EMEP and EANET monitoring networks. The impactor channel was upgraded to separate particles bigger than 1 mkm in size, and the fine grain fraction settled down on it. Reverse 5-day and 10-day trajectories of air mass transfer executed at heights of 10, 1500 and 3500 m were analyzed. The heights were selected by considerations that 3000 m is the height which characterizes air mass trend in the lower troposphere. 1500 m is the upper border of the atmospheric boundary layer, and the sampling was done in the Earth's surface layer at less than 10 m. Minimum values of the bespoken microphysical characteristics are better characteristic of higher latitudes where there are no man induced sources of

  9. Variability in aerosol optical and physical characteristics over the Bay of Bengal and the Arabian Sea deduced from Ångström exponents

    NASA Astrophysics Data System (ADS)

    Kedia, Sumita; Ramachandran, S.

    2009-07-01

    Spectral distribution of aerosol optical depths (AODs) measured in the 0.4-0.875 μm wavelength region using a Sun photometer over Bay of Bengal and Arabian Sea during the 2006 premonsoon season are analyzed to obtain more interesting information on the physical and optical characteristics of aerosols. Examination of spectral AODs measured over the Bay of Bengal and the Arabian Sea by deriving the Ångström exponent (α) for the entire spectral range (0.4-0.875 μm), α for different spectral ranges, and second derivative (α') showed that the aerosol size distribution is of mixed type or bimodal with contributions from fine and coarse modes. The α-AOD relationships in short (0.4-0.5 μm), long (0.65-0.9 μm), and full (0.4-0.9 μm) spectral ranges determined for various aerosol models (urban, maritime clean, maritime polluted, and desert) suggest that the α-AOD relationship can vary depending on whether the size distribution is unimodal, mixed type, or bimodal, similar to the results obtained for measured AOD spectra. Significant curvature in the ln AOD versus ln λ is observed which causes spectral variation in α derived in different spectral ranges. Over the Bay of Bengal for 76% of AOD spectra, α2 - α1 is >1, suggesting the presence of fine-mode aerosols from a wide variety of fine-mode fractions or a mixture of modes, while over the Arabian Sea, α2 - α1 is <1 for 84% of AOD spectra, clearly indicating the dominance of coarse-mode aerosols. These characteristics can be used in modeling the regional and seasonal aerosol radiative effects and in remote sensing.

  10. Aerosol Size Distribution Response to Anthropogenically Driven Historical Changes in Biogenic Secondary Organic Aerosol Formation

    NASA Astrophysics Data System (ADS)

    Pierce, J. R.; D'Andrea, S.; Acosta Navarro, J. C.; Farina, S.; Scott, C.; Farmer, D. K.; Spracklen, D. V.; Riipinen, I.

    2014-12-01

    Emissions of biological volatile organic compounds (BVOC) have changed in the past millennium due to changes in land use, temperature and CO2 concentrations. A recent model reconstruction of BVOC emissions over the past millennium predicted the changes in the three dominant secondary organic aerosol (SOA) producing BVOC classes (isoprene, monoterpenes and sesquiterpenes). The reconstruction predicted that in global averages isoprene emissions have decreased (land-use changes to crop/grazing land dominate the reduction), while monoterpene and sesquiterpene emissions have increased (temperature increases dominate the increases); however, all three show both increases and decreases in certain regions due to competition between the various influencing factors. These BVOC changes have largely been anthropogenic in nature, and land-use change was shown to have the most dramatic effect by decreasing isoprene emissions. We use these modeled estimates of these three dominant BVOC classes' emissions from the years 1000 to 2000 to test the effect of anthropogenic changes to BVOC emissions on SOA formation and global aerosol size distributions using the GEOS-Chem-TOMAS global aerosol microphysics model. With anthropogenic emissions (e.g. SO2, NOx, primary aerosols) held at present day values and BVOC emissions changed from year 1000 to year 2000 values, decreases in the number concentration of particles of size Dp > 80 nm (N80) of >25% in year 2000 relative to year 1000 were predicted in regions with extensive land-use changes since year 1000. This change in N80 was predominantly driven by a shift towards crop/grazing land that produces less BVOC than the natural vegetation. Similar sensitivities to year 1000 vs. year 2000 BVOC emissions exist when anthropogenic emissions are turned off. This large decrease in N80 could be a largely overlooked and important anthropogenic aerosol effect on regional climates.

  11. Effect of secondary organic aerosol amount and condensational behavior on global aerosol size distributions

    NASA Astrophysics Data System (ADS)

    D'Andrea, S. D.; Häkkinen, S. A. K.; Westervelt, D. M.; Kuang, C.; Spracklen, D. V.; Riipinen, I.; Pierce, J. R.

    2013-05-01

    Recent research has shown that secondary organic aerosols (SOA) are major contributors to ultrafine particle growth to climatically relevant sizes, increasing global cloud condensation nuclei (CCN) concentrations within the continental boundary layer. Many models treat SOA solely as semivolatile, which leads to condensation of SOA proportional to the aerosol mass distribution; however, recent closure studies with field measurements show that a significant fraction of SOA condenses proportional to the aerosol surface area, which suggests a very low volatility. Additionally, while many global models contain only biogenic sources of SOA (with emissions generally 10-30 Tg yr-1), recent studies have shown a need for an additional source of SOA around 100 Tg yr-1 correlated with anthropogenic carbon monoxide (CO) emissions is required to match measurements. Here, we explore the significance of these two findings using the GEOS-Chem-TOMAS global aerosol microphysics model. The percent change in the number of particles of size Dp > 40 nm (N40) within the continental boundary layer between the surface-area-and massdistribution condensation schemes, both with the base biogenic SOA only, yielded a global increase of 8% but exceeds 100% in biogenically active regions. The percent change in N40 within the continental boundary layer between the base simulation (19 Tg yr-1) and the additional SOA (100 Tg yr-1) both using the surface area condensation scheme (very low volatility) yielded a global increase of 14%, and a global decrease in the number of particles of size Dp > 10 nm (N10) of 32%. These model simulations were compared to measured data from Hyytiälä, Finland and other global locations and confirmed a decrease in the model-measurement bias. Thus, treating SOA as very low volatile as well as including additional SOA correlated with anthropogenic CO emissions causes a significant global increase in the number of climatically relevant sized particles, and therefore we

  12. Effect of In-Plume Aerosol Processing on the Efficacy of Marine Cloud Albedo Enhancement from Controlled Sea-Spray Injections

    NASA Astrophysics Data System (ADS)

    Stevens, R. G.; Spracklen, D.; Korhonen, H.; Pierce, J. R.

    2010-12-01

    The intentional enhancement of cloud albedo via controlled sea-spray injection from ships has been suggested as a possible means to control anthropogenic global warming (1); however, there remains significant uncertainty in the efficacy of this method due to uncertainties in aerosol and cloud microphysics. Recent analysis showed that more sea-spray may be necessary than previously assumed to reach a desired cooling due to nonlinearities in the aerosol/cloud microphysics (2). A major assumption used in (2) is that all sea-spray was emitted uniformly into some oceanic grid boxes, and thus did not account for sub-grid aerosol microphysics within the sea-spray plumes. However, as a consequnce of the fast sea-spray injection rates which are proposed, in the order of 1x10^17 1/s (1), particle concentrations in these plumes may be quite high and particle coagulation may significantly reduce the number of emitted particles and increase their average size. Therefore, it is possible that the emissions necessary to reach a desired cooling may be even larger than currently assumed. We explore the processing of the freshly emitted sea-spray plumes in the Large-Eddy Simulation (LES)/Cloud Resolving Model (CRM) the System for Atmospheric Modelling (SAM, 3) with the online aerosol microphysics module TOMAS (4). We determine how the final number and size of particles (once well mixed with background air) depends on the emission rate and size distribution of the sea-spray plume and on the pre-existing aerosol concentrations and local atmospheric conditions. Finally, we make suggestions for effective size-resolved emissions for use in climate models. (1) Salter, S. et al., Phil. Trans. R. Soc. A., 2008. (2) Korhonen, H. et al., Atmos. Chem. Phys., 10, 4133-4143, 2010. (3) Khairoutdinov, M., and Randall, D.,. J. Atmos. Sci., 60, 607-625, 2003. (4) Pierce, J. and Adams, P., Atmos. Chem. Phys., 9, 1339-1356, 2009.

  13. Analysis of Aerosol Physical and Chemical Properties on the Coast of the Japanese Sea (Tango peninsula) during ACE-Asia

    NASA Astrophysics Data System (ADS)

    Tohno, S.; Hoeller, R.; Ito, K.; Onishi, Y.; Ma, C. J.; Kasahara, M.; Cahill, T. A.; Cliff, S.

    2001-12-01

    During springtime the Japanese archipelago is periodically influenced by haze events originating from the Asian continent. The sources of these materials include both anthropogenic and natural aerosol, including the well-known yellow sand (Kosa) events, which can be recognized at places as far as Hawaii and the west coast of the United States. But there is also strong evidenced, which we want to support in this study, that these Kosa events are accompanied by strongly absorbing material as well as sulfates and organics. The springtime of 2001 was characterized by several strong dust events, which happened to be during the international ACE-Asia campaign. We participated in the ACE observation network by setting up a monitoring station during the period March 19 to April 6, 2001 for the measurement of aerosol optical, physical and chemical properties as well as observations of sky radiation. The measurement site is located on the coast of the Japanese Sea (Tango Peninsula, Kyoto Prefecture). Tango was chosen as an observation site, since it is relatively unpolluted and can therefore serve as a background site for studies of the direct impact of the mainland Asian outflow on the western Pacific area. The purpose of this work is to perform local and column closure experiments on aerosol properties, and to distinguish the anthropogenic part of the aerosol from the natural one. For this purpose, backward air-mass trajectories are calculated to identify potential sources of the observed aerosol. For measurements of aerosol mass-size distributions we used 12-stage low-pressure impactors, which were subsequently analyzed for elemental and ionic concentrations by PIXE, and Ion-chromatography, respectively. In addition, to get both the necessary time- and size-resolution, a DRUM sampler was operated with continuous collection and analysis for mass and optical transmission from 320 nm to 850 nm. Analysis is scheduled by synchrotron-XRF to < 0.1 ng/m3 for trace elemental

  14. Comparative Climate Responses of Anthropogenic Greenhouse Gases, All Major Aerosol Components, Black Carbon, and Methane, Accounting for the Evolution of the Aerosol Mixing State and of Clouds/Precipitation from Multiple Aerosol Size Distributions

    NASA Astrophysics Data System (ADS)

    Jacobson, M. Z.

    2005-12-01

    Several modeling studies to date have simulated the global climate response of anthropogenic greenhouse gases and bulk (non-size-resolved) sulfate or generic aerosol particles together, but no study has examined the climate response of greenhouse gases simultaneously with all major size- and composition resolved aerosol particle components. Such a study is important for improving our understanding of the effects of anthropogenic pollutants on climate. Here, the GATOR-GCMOM model is used to study the global climate response of (a) all major greenhouse gases and size-resolved aerosol components, (b) all major greenhouse gases alone, (c) fossil-fuel soot (black carbon, primary organic matter, sulfuric acid, bisulfate, sulfate), and (d) methane. Aerosol components treated in all simulations included water, black carbon, primary organic carbon, secondary organic carbon, sulfuric acid, bisulfate, sulfate, nitrate, chloride, ammonium, sodium, hydrogen ion, soil dust, and pollen/spores. Fossil-fuel soot (FFS) was emitted into its own size distribution. All other components, including biofuel and biomass soot, sea-spray, soil dust, etc., were emitted into a second distribution (MIX). The FFS distribution grew by condensation of secondary organic matter and sulfuric acid, hydration of water, and dissolution of nitric acid, ammonia, and hydrochloric acid. It self-coagulated and heterocoagulated with the MIX distribution, which also grew by condensation, hydration, and dissolution. Treatment of separate distributions for FFS allowed FFS to evolve from an external mixture to an internal mixture. In both distributions, black carbon was treated as a core component for optical calculations. Both aerosol distributions served as CCN during explicit size-resolved cloud formation. The resulting clouds grew by coagulation and condensation, coagulated with interstitial aerosol particles, and fell to the surface as rain and snow, carrying aerosol constituents with them. Thus, cloud

  15. Arabian Sea tropical cyclones intensified by emissions of black carbon and other aerosols.

    PubMed

    Evan, Amato T; Kossin, James P; Chung, Chul Eddy; Ramanathan, V

    2011-11-02

    Throughout the year, average sea surface temperatures in the Arabian Sea are warm enough to support the development of tropical cyclones, but the atmospheric monsoon circulation and associated strong vertical wind shear limits cyclone development and intensification, only permitting a pre-monsoon and post-monsoon period for cyclogenesis. Thus a recent increase in the intensity of tropical cyclones over the northern Indian Ocean is thought to be related to the weakening of the climatological vertical wind shear. At the same time, anthropogenic emissions of aerosols have increased sixfold since the 1930s, leading to a weakening of the southwesterly lower-level and easterly upper-level winds that define the monsoonal circulation over the Arabian Sea. In principle, this aerosol-driven circulation modification could affect tropical cyclone intensity over the Arabian Sea, but so far no such linkage has been shown. Here we report an increase in the intensity of pre-monsoon Arabian Sea tropical cyclones during the period 1979-2010, and show that this change in storm strength is a consequence of a simultaneous upward trend in anthropogenic black carbon and sulphate emissions. We use a combination of observational, reanalysis and model data to demonstrate that the anomalous circulation, which is radiatively forced by these anthropogenic aerosols, reduces the basin-wide vertical wind shear, creating an environment more favourable for tropical cyclone intensification. Because most Arabian Sea tropical cyclones make landfall, our results suggest an additional impact on human health from regional air pollution.

  16. Updating sea spray aerosol emissions in the Community Multiscale Air Quality (CMAQ) model

    EPA Science Inventory

    Sea spray aerosols (SSA) impact the particle mass concentration and gas-particle partitioning in coastal environments, with implications for human and ecosystem health. In this study, the Community Multiscale Air Quality (CMAQ) model is updated to enhance fine mode SSA emissions,...

  17. Aged boreal biomass burning aerosol size distributions from BORTAS 2011

    NASA Astrophysics Data System (ADS)

    Sakamoto, K. M.; Allan, J. D.; Coe, H.; Taylor, J. W.; Duck, T. J.; Pierce, J. R.

    2014-09-01

    Biomass-burning aerosols contribute to aerosol radiative forcing on the climate system. The magnitude of this effect is partially determined by aerosol size distributions, which are functions of source fire characteristics (e.g. fuel type, MCE) and in-plume microphysical processing. The uncertainties in biomass-burning emission number size-distributions in climate model inventories lead to uncertainties in the CCN concentrations and forcing estimates derived from these models. The BORTAS-B measurement campaign was designed to sample boreal biomass-burning outflow over Eastern Canada in the summer of 2011. Using these BORTAS-B data, we implement plume criteria to isolate the characteristic size-distribution of aged biomass-burning emissions (aged ∼1-2 days) from boreal wildfires in Northwestern Ontario. The composite median size-distribution yields a single dominant accumulation mode with Dpm = 230 nm (number-median diameter), σ = 1.7, which are comparable to literature values of other aged plumes of a similar type. The organic aerosol enhancement ratios (ΔOA / ΔCO) along the path of Flight b622 show values of 0.05-0.18 μg m-3 ppbv-1 with no significant trend with distance from the source. This lack of enhancement ratio increase/decrease with distance suggests no detectable net OA production/evaporation within the aged plume over the sampling period. A Lagrangian microphysical model was used to determine an estimate of the freshly emitted size distribution corresponding to the BORTAS-B aged size-distributions. The model was restricted to coagulation and dilution processes based on the insignificant net OA production/evaporation derived from the ΔOA / ΔCO enhancement ratios. We estimate that the fresh-plume median diameter was in the range of 59-94 nm with modal widths in the range of 1.7-2.8 (the ranges are due to uncertainty in the entrainment rate). Thus, the size of the freshly emitted particles is relatively unconstrained due to the uncertainties in

  18. Responses of phytoplankton community to the input of different aerosols in the East China Sea

    NASA Astrophysics Data System (ADS)

    Meng, X.; Chen, Y.; Wang, B.; Ma, Q. W.; Wang, F. J.

    2016-07-01

    Atmospheric deposition can affect marine phytoplankton by supplying macronutrients and trace elements. We conducted mesocosm experiments by adding aerosols with different composition (dominated by mineral dust, biomass burning and high Cu, and secondary aerosol, respectively) to the surface seawater of the East China Sea. Chlorophyll a concentrations were found to be the highest and lowest after adding aerosols containing the highest Fe and dissolved inorganic nitrogen (DIN), respectively. The relative abundance of Haptophyceae increased significantly after adding mineral dust, whereas diatom, Dinophyceae and Cryptophyceae reached the maximum accompanied with the highest DIN. Our results suggest that Fe may be more important than DIN in promoting primary productivity in the sampled seawater. The input of mineral dust and anthropogenic aerosols may result in distinct changes of phytoplankton community structure.

  19. Evaluation of aerosol distributions in the GISS-TOMAS global aerosol microphysics model with remote sensing observations

    NASA Astrophysics Data System (ADS)

    Lee, Y. H.; Adams, P. J.

    2009-09-01

    The Aerosol Optical Depth (AOD) and Angstrom Coefficient (AC) predictions in the GISS-TOMAS model of global aerosol microphysics are evaluated against remote sensing data from MODIS, MISR, and AERONET. The model AOD agrees well (within a factor of two) over polluted continental (or high sulfate), dusty, and moderate sea-salt regions but less well over the equatorial, high sea-salt, and biomass burning regions. Underprediction of sea-salt in the equatorial region is likely due to GCM meteorology (low wind speeds and high precipitation). For the Southern Ocean, overprediction of AOD is very likely due to high sea-salt emissions and perhaps aerosol water uptake in the model. However, uncertainties in cloud screening in high latitude make it difficult to evaluate the model AOD at high latitudes with the satellite-based AOD. AOD in biomass burning regions is underpredicted, a problem also seen in other global aerosol models but more severely in this work. Using measurements from the LBA-SMOCC 2002 campaign, the surface-level OC and EC concentrations in the model are found to be underpredicted severely during the dry season, suggesting the low AOD in the model is due to underpredictions in OM and EC mass. These, in turn, result from unrealistically short wet deposition lifetimes during the dry season in the GCM.

  20. Seasonal and spatial distribution of arctic aerosols observed by CALIOP (2006-2011)

    NASA Astrophysics Data System (ADS)

    Di Pierro, M.; Jaegle, L.

    2012-12-01

    The Arctic is a known receptor of aerosol and gaseous pollutants emitted in the mid-latitudes. Surface observations in the high Arctic (>70°N) show a distinct seasonality at the surface, with maxima in aerosol extinction in winter-early spring and minima in summer. The spatial and temporal distribution of Arctic aerosols remains poorly constrained even at the surface, especially in the Siberian sector, whereas in the free troposphere aerosols observations are even sparser in space and time. Here, we use retrievals from the Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP) on board the CALIPSO satellite to explore the spatial and temporal variability of arctic aerosols from the surface to 8 km altitude over a 5-year period (2006-2011). We develop an empirical method taking into account the difference in performance between daytime and nighttime CALIOP retrievals. We validate this method by comparing CALIOP's retrieved aerosol extinction against ground-based observations at Barrow (Alaska), Alert and Eureka (Canada) as well as aircraft observations obtained during NASA's ARCTAS mission over the Canadian and Alaskan Arctic. Our study highlights a different seasonality in the free troposphere than near the surface and also significant differences between the seasonality in the low (60°-70°N) and high (70°-82°N) Arctic. In the high Arctic near the surface, extinction reaches a maximum in winter and a minimum in summer. The summer minimum is not observed in the low Arctic. Instead a July maximum is observed associated with the burning of biomass in boreal forests. In the free troposphere, the maximum in extinction occurs in March-April (2-5 km), and April-May (5-8 km). A relatively small interannual variability is observed, particularly in the high Arctic. A strong gradient in aerosol extinction is seen between 60°N and 70°N in the summer, which we attribute to efficient local wet scavenging at high latitudes by stratocumulus drizzle. Biomass burning

  1. The sea ice thickness distribution in the northwestern Weddell Sea

    NASA Astrophysics Data System (ADS)

    Lange, M. A.; Eicken, H.

    1991-03-01

    We present new data on distribution of snow and sea ice thicknesses in the northwestern Weddell Sea. The data were obtained through direct measurements along 19 profiles, each approximately 100 m long on 17 different floes located between 54°-46°W and 59°-64°S. The overall probability density functions (PDFs) for ice thicknesses reflect the complex mixture of first-, second-, and multi-year ice to be expected in the outflowing branch of the Weddell Gyre. Further differentiation of the data reveals four distinct thickness classes which reflect differences in the formation and subsequent histories of the ice encountered. These classes (I-IV) represent strongly deformed first year ice, less deformed first- and second-year ice, and deformed second- or multi-year ice, respectively. Each of the classes is characterized by a specific set of quantities related to ice texture and surface snow characteristics and by distinct PDFs for snow and ice thicknesses. In addition, geometric surface and bottom roughness characteristics differ significantly for each of the floe classes.

  2. Parameter sensitivity study of Arctic aerosol vertical distribution in CAM5

    NASA Astrophysics Data System (ADS)

    Jiao, C.; Flanner, M.

    2015-12-01

    Arctic surface temperature response to light-absorbing aerosols (black carbon, brown carbon and dust) depends strongly on their vertical distributions. Improving model simulations of three dimensional aerosol fields in the remote Arctic region will therefore lead to improved projections of the climate change caused by aerosol emissions. In this study, we investigate how different physical parameterizations in the Community Atmosphere Model version 5 (CAM5) influence the simulated vertical distribution of Arctic aerosols. We design experiments to test the sensitivity of the simulated aerosol fields to perturbations of selected aerosol process-related parameters in the Modal Aerosol Module with seven lognormal modes (MAM7), such as those govern aerosol aging, in-cloud and below-cloud scavenging, aerosol hygroscopicity and so on. The simulations are compared with observed aerosol vertical distributions and total optical depth to assess model performance and quantify uncertainties associated with these model parameterizations. Observations applied here include Arctic aircraft measurements of black carbon and sulfate vertical profiles, along with Aerosol Robotic Network (AERONET) optical depth measurements. We also assess the utility of using High Spectral Resolution Lidar (HSRL) measurements from the ARM Barrow site to infer vertical profiles of aerosol extinction. The sensitivity study explored here will provide guidance for optimizing global aerosol simulations.

  3. Comparing Organic Aerosol Composition from Marine Biogenic Sources to Seawater and to Physical Sea Spray Models

    NASA Astrophysics Data System (ADS)

    Russell, L. M.; Frossard, A. A.; Sanchez, K.; Massoli, P.; Elliott, S.; Burrows, S. M.; Bates, T. S.; Quinn, P.

    2015-12-01

    In much of the marine atmosphere, organic components in aerosol particles have many sources other than sea spray that contribute organic constituents. For this reason, physical sea spray models provide an important technique for studying the organic composition of particles from marine biogenic sources. The organic composition of particles produced by two different physical sea spray models were measured in three open ocean seawater types: (i) Coastal California in the northeastern Pacific, which is influenced by wind-driven, large-scale upwelling leading to productive or eutrophic (nutrient-rich) seawater and high chl-a concentrations, (ii) George's Bank in the northwestern Atlantic, which is also influenced by nutrient upwelling and eutrophic seawater with phytoplankton productivity and high chl-a concentrations, and (iii) the Sargasso Sea in the subtropical western Atlantic, which is oligotrophic and nutrient-limited, reflected in low phytoplankton productivity and low chl-a concentrations. Fourier transform infrared spectroscopy provides information about the functional group composition that represents the marine organic fraction more completely than is possible with techniques that measure non-refractory mass (vaporizable at 650°C). After separating biogenic marine particles from those from other sources, the measured compositions of atmospheric marine aerosol particles from three ocean regions is 65±12% hydroxyl, 21±9% alkane, 6±6% amine, and 7±8% carboxylic acid functional groups. The organic composition of atmospheric primary marine (ocean-derived) aerosol particles is nearly identical to model generated primary marine aerosol particles from bubbled seawater. Variability in productive and non-productive seawater may be caused by the presence of surfactants that can stabilize the bubble film and lead to preferential drainage of the more soluble (lower alkane group fraction) organic components without substantial changes in overall group composition

  4. Quantifying the climatological cloud-free direct radiative forcing of aerosol over the Red Sea

    NASA Astrophysics Data System (ADS)

    Brindley, Helen; Osipov, Serega; Bantges, Richard; Smirnov, Alexander; Banks, Jamie; Levy, Robert; Prakash, P.-Jish; Stenchikov, Georgiy

    2015-04-01

    A combination of ground-based and satellite observations are used, in conjunction with column radiative transfer modelling, to assess the climatological aerosol loading and quantify its corresponding cloud-free direct radiative forcing (DRF) over the Red Sea. While there have been campaigns designed to probe aerosol-climate interactions over much of the world, relatively little attention has been paid to this region. Because of the remoteness of the area, satellite retrievals provide a crucial tool for assessing aerosol loading over the Sea. However, agreement between aerosol properties inferred from measurements from different instruments, and even in some cases from the same measurements using different retrieval algorithms can be poor, particularly in the case of mineral dust. Ground based measurements which can be used to evaluate retrievals are thus highly desirable. Here we take advantage of ship-based sun-photometer micro-tops observations gathered from a series of cruises which took place across the Red Sea during 2011 and 2013. To our knowledge these data represent the first set of detailed aerosol measurements from the Sea. They thus provide a unique opportunity to assess the performance of satellite retrieval algorithms in this region. Initially two aerosol optical depth (AOD) retrieval algorithms developed for the MODerate Resolution Imaging Spectroradiometer (MODIS) and Spinning Enhanced Visible and InfraRed Imager (SEVIRI) instruments are evaluated via comparison with the co-located cruise observations. These show excellent agreement, with correlations typically better than 0.9 and very small root-mean-square and bias differences. Calculations of radiative fluxes and DRF along one of the cruises using the observed aerosol and meteorological conditions also show good agreement with co-located estimates from the Geostationary Earth Radiation Budget (GERB) instrument if the aerosol asymmetry parameter is adjusted to account for the presence of large

  5. 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.

  6. Distributed Regional Aerosol Gridded Observation Network (DRAGON) - Korea 2012 campaign

    NASA Astrophysics Data System (ADS)

    Kim, J.; Holben, B. N.; Eck, T. F.; Jeong, U.; Kim, W. V.; Choi, M.; Kim, D. S.; Kim, B.; Kim, S.; Ghim, Y.; Kim, Y. J.; Kim, J. H.; Park, R.; Seo, M.; Song, C.; Yum, S.; Woo, J.; Yoon, S.; Lee, K.; Lee, M.; Lim, J.; Chang, I.; Jeong, M. J.; Bae, M.; Sorokin, M.; Giles, D. M.; Schafer, J.; Herman, J. R.

    2013-12-01

    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. Recently, with the cooperative efforts with NASA (National Aeronautics and Space Administration) / GSFC (Goddard Space Flight Center), Korean University research groups, and KME (Korea Ministry of Environment) / NIER (National Institute of Environmental Research), DRAGON-Korea 2012 campaign was successfully performed from March to May 2012. The campaign sites were divided into two groups, the National scale sites and Seoul metropolitan sites. Thirteen Cimel sunphotometers were distributed at National scale sites including two metropolitan cities and several remote sites. Nine Cimel sunphotometers were distributed at Seoul Metropolitan sites including several residential sites and traffic source areas. The measured datasets are being analyzed in diverse fields of air quality communities including in-situ measurement groups, satellite remote sensing groups, chemical modeling groups, and airplane measurement groups. We will introduce several preliminary results of the analysis and discuss the future planes and corporations in Korea.

  7. Distribution and clearance of radioactive aerosol on the nasal mucosa.

    PubMed

    McLean, J A; Bacon, J R; Mathews, K P; Thrall, J H; Banas, J M; Hedden, J; Bayne, N K

    1984-03-01

    The distribution and clearance of aerosolized radioactive technetium 99m pertechnate in physiologic buffered saline was analyzed in four human adult asymptomatic volunteers following delivery into one nostril in the same manner as for nasal challenge testing (i.e., 0.1 ml via a 251 DeVilbiss atomizer powered by a compressor delivering 0.10 +/- 0.01 gm/spray). For comparison, squeeze bottles and spray bottles from commercial sources, a 114 and a 127 DeVilbiss atomizer, and a pipette were employed. Lateral imagery via minicomputer processing was used to determine both distribution and clearance of the radiotracer. The counts after 1 minute were lower following pipette delivery than with the other devices. None yielded discernable , wide-spread distribution of aerosol throughout the nasal cavity. Following delivery from the 251 atomizer, mean clearance at 17 minutes was 60.0%. Similar clearance rates were obtained with the other spraying methods except for lower values with the squeeze bottle. Analysis of six hour clearance studies by linear regression showed a relatively rapid initial phase, which is probably due largely to mucociliary clearance, and a prolonged late phase related to the very slow disappearance of residual material located far anteriorly in the nose. Achieving good initial retention and rapid clearance of material deposited anteriorly in the nose are desirable attributes of devices employed for administering materials intranasally.

  8. Biogenic, anthropogenic and sea salt sulfate size-segregated aerosols in the Arctic summer

    NASA Astrophysics Data System (ADS)

    Ghahremaninezhad, Roghayeh; Norman, Ann-Lise; Abbatt, Jonathan P. D.; Levasseur, Maurice; Thomas, Jennie L.

    2016-04-01

    Size-segregated aerosol sulfate concentrations were measured on board the Canadian Coast Guard Ship (CCGS) Amundsen in the Arctic during July 2014. The objective of this study was to utilize the isotopic composition of sulfate to address the contribution of anthropogenic and biogenic sources of aerosols to the growth of the different aerosol size fractions in the Arctic atmosphere. Non-sea-salt sulfate is divided into biogenic and anthropogenic sulfate using stable isotope apportionment techniques. A considerable amount of the average sulfate concentration in the fine aerosols with a diameter < 0.49 µm was from biogenic sources (> 63 %), which is higher than in previous Arctic studies measuring above the ocean during fall (< 15 %) (Rempillo et al., 2011) and total aerosol sulfate at higher latitudes at Alert in summer (> 30 %) (Norman et al., 1999). The anthropogenic sulfate concentration was less than that of biogenic sulfate, with potential sources being long-range transport and, more locally, the Amundsen's emissions. Despite attempts to minimize the influence of ship stack emissions, evidence from larger-sized particles demonstrates a contribution from local pollution. A comparison of δ34S values for SO2 and fine aerosols was used to show that gas-to-particle conversion likely occurred during most sampling periods. δ34S values for SO2 and fine aerosols were similar, suggesting the same source for SO2 and aerosol sulfate, except for two samples with a relatively high anthropogenic fraction in particles < 0.49 µm in diameter (15-17 and 17-19 July). The high biogenic fraction of sulfate fine aerosol and similar isotope ratio values of these particles and SO2 emphasize the role of marine organisms (e.g., phytoplankton, algae, bacteria) in the formation of fine particles above the Arctic Ocean during the productive summer months.

  9. Different responses of Sea Surface Temperature in the North Pacific to greenhouse gas and aerosol forcing

    NASA Astrophysics Data System (ADS)

    Wang, Liyi; Liu, Qinyu

    2015-12-01

    The responses of Sea Surface Temperature (SST) to greenhouse gas (GHG) and anthropogenic aerosol in the North Pacific are compared based on the historical single and all-forcing simulations with Geophysical Fluid Dynamics Laboratory Climate Model version 3 (GFDL CM3). During 1860-2005, the effect of GHG forcing on the North Pacific SST is opposite to that of the aerosol forcing. Specifically, the aerosol cooling effect exceeds the GHG warming effect in the Kuroshio Extension (KE) region during 1950-2004 in the CM3 single forcing. The mid-latitude response of ocean circulation to the GHG (aerosol) forcing is to enhance (weaken) the Subtropical Gyre. Then the SST warming (cooling) lies on the zonal band of 40°N because of the increased (reduced) KE warm advection effect in the GHG (aerosol) forcing simulations, and the cooling effect to SST will surpass the warming effect in the KE region in the historical all-forcing simulations. Besides, the positive feedback between cold SST and cloud can also strengthen the aerosol cooling effect in the KE region during boreal summer, when the mixed layer depth is shallow. In the GHG (aerosol) forcing simulations, corresponding to warming (cooling) SST in the KE region, the weakened (enhanced) Aleutian Low appears in the Northeast Pacific. Consequently, the SST responses to all-forcing in the historical simulations are similar to the responses to aerosol forcing in sign and spatial pattern, hence the aerosol effect is quite important to the SST cooling in the mid-latitude North Pacific during the past 55 years.

  10. Aerosol Optical Thickness From the SeaWiFS and MODIS Sensors Over the Chesapeake Bay

    NASA Astrophysics Data System (ADS)

    Ahmad, Z.; Kwiatkowska, E.; Franz, B. A.; McClain, C. R.

    2006-12-01

    Presently, a suite of 12 aerosol models are used for atmospheric correction purposes to retrieve water-leaving radiances in the visible and near IR spectral bands of the SeaWiFS and MODIS sensors. These models are based on Shettle and Fenn's (1979) aerosol models of tropospheric and oceanic aerosols. As a part of the atmospheric correction effort, the Ocean Biology Processing Group (OBPG) also reports the aerosol optical thickness (AOT) for the scene. We have compared the AOT from the SeaWiFS and MODIS with the AERONET retrievals over the Chesapeake Bay, and found that the satellite-retrieved AOT in the 865/869 bands of SeaWiFS/MODIS sensors are generally higher than the AERONET retrievals. We attribute the overestimation of AOT mostly due to the backscattering of downwelling solar irradiance by phytoplankton, CDOM and non-algal suspended particles in the Bay. Results from simulation studies, and from the comparison of satellite-derived AOT and the AERONET in the visible and near IR bands will be presented.

  11. Role of Organic Coatings in Regulating N2O5 Reactive Uptake to Sea Spray Aerosol.

    PubMed

    Ryder, Olivia S; Campbell, Nicole R; Morris, Holly; Forestieri, Sara; Ruppel, Matthew J; Cappa, Christopher; Tivanski, Alexei; Prather, Kimberly; Bertram, Timothy H

    2015-12-01

    Previous laboratory measurements and field observations have suggested that the reactive uptake of N2O5 to sea spray aerosol particles is a complex function of particle chemical composition and phase, where surface active organics can suppress the reactive uptake by up to a factor of 60. To date, there are no direct studies of the reactive uptake of N2O5 to nascent sea spray aerosol that permit assessment of the role that organic molecules present in sea spray aerosol (SSA) may play in suppressing or enhancing N2O5 uptake kinetics. In this study, SSA was generated from ambient seawater and artificial seawater matrices using a Marine Aerosol Reference Tank (MART), capable of producing nascent SSA representative of ambient conditions. The reactive uptake coefficient of N2O5 (γ(N2O5)) on nascent SSA was determined using an entrained aerosol flow reactor coupled to a chemical ionization mass spectrometer for measurement of surface area dependent heterogeneous loss rates. Population averaged measurements of γ(N2O5) for SSA generated from salt water sequentially doped with representative organic molecular mimics, or from ambient seawater, do not deviate statistically from that observed for sodium chloride (γ(N2O5)NaCl = 0.01-0.03) for relative humidity (RH) ranging between 50 and 65%. The results are consistent with measurements made under clean marine conditions at the Scripps Institution of Oceanography Pier and those conducted on nascent SSA generated in the marine aerosol reference tank. The results presented here suggest that organic films present on nascent SSA (at RH greater than 50%) likely do not significantly limit N2O5 reactive uptake.

  12. The Effect of Changes in Polar Sea Ice on Emissions of Marine Aerosols

    NASA Astrophysics Data System (ADS)

    Matrai, P.; Gabric, A. J.

    2015-12-01

    Cloud radiative effects remain a major weakness in our understanding of the climate system and consequently in developing accurate climate projections. This is mainly true for Arctic low-level clouds in their key role of regulating surface energy fluxes which affect the freezing and melting of sea ice. The radiative properties of clouds are strongly dependent on the number concentration of airborne water-soluble particles, known as cloud condensation nuclei (CCN). In the Arctic, the aerosol-cloud-radiation relationship is more complex than elsewhere and the clouds constitute a warming factor for climate, rather than cooling, most of the year. This is due to the semi-permanent ice cover, which raises the albedo of the surface, and the clean Arctic air, which decreases the albedo of the clouds. There has been much discussion on the relative magnitude of the biogenic source of polar CCN: Primary organic marine aerosols and/or sulfate-containing aerosols, derived from marine emissions. Regional field measurements and pan- (Ant)Arctic model simulations don't necessarily agree. Arctic CCN are formed primarily by aggregates of marine organic material and may grow in mass by condensation. Southern Ocean aerosols may be dominated by sulfate particles and organic particles at lower and higher Antarctic latitudes, respectively. The interaction of polar marine microorganisms, seasonality, sea ice cover, presence or absence of sea spray, and atmospheric heterogeneous processes combine to control natural aerosol concentrations and mass, thus modulating the sensitivity of cloud properties, including their reflectivity and the resulting regional radiation budget. We discuss Arctic and Antarctic field and satellite observations and establish a strong and fundamental link between the biology at the ocean/sea ice interface, clouds and climate over polar regions.

  13. Tying Biological Activity to Changes in Sea Spray Aerosol Chemical Composition via Single Particle Analyses

    NASA Astrophysics Data System (ADS)

    Sultana, C. M.; Lee, C.; Collins, D. B.; Axson, J. L.; Laskina, O.; Grandquist, J. R.; Grassian, V. H.; Prather, K. A.

    2014-12-01

    In remote marine environments, sea spray aerosols (SSA) often represent the greatest aerosol burden, thus having significant impacts on direct radiative interactions and cloud processes. Previous studies have shown that SSA is a complex mixture of inorganic salts and an array of dissolved and particulate organic components. Enrichment of SSA organic content is often correlated to seawater chlorophyll concentrations, a measure of oceanic biological activity. As the physical and chemical properties of aerosols control their radiative effects, recent studies conducted by the Center for Aerosol Impacts on Climate and the Environment have endeavored to further elucidate the ties between marine biological activity and primary SSA chemical composition using highly time resolved single particle analyses. A series of experiments performed in the recently developed Marine Aerosol Reference Tank evaluated the effect of changing marine microbial populations on SSA chemical composition, which was monitored via an aerosol time-of-flight mass spectrometer and a variety of offline spectroscopic and microscopic techniques. Each experiment was initiated using unfiltered and untreated seawater, thus maintaining a high level of biogeochemical complexity. This study is the first of its kind to capture daily changes in the primary SSA mixing state over the growth and death of a natural phytoplankton bloom. Increases in organic aerosol types (0.4-3 μm), internally and externally mixed with sea salt, could not be correlated to chlorophyll concentrations. Maximum production of these populations occurred two to four days after the in vivo chlorophyll fluorescence peaked in intensity. This work is in contrast to the current paradigm of correlating SSA organic content to seawater chlorophyll concentration.

  14. Features of aerosol optical depths over the Bay of Bengal and the Arabian Sea during premonsoon season: Variabilities and anthropogenic influence

    NASA Astrophysics Data System (ADS)

    Kedia, Sumita; Ramachandran, S.

    2008-06-01

    Spectral aerosol optical depths (AOD) measured on board a cruise over the Bay of Bengal and the Arabian Sea during March-May 2006 are analyzed. Mean 0.5 μm AOD over the Bay of Bengal is higher (0.36) than the Arabian Sea (0.25). AODs obtained from MODIS Terra and Aqua are found to track well the Sun photometer AODs. A comparison between Sun photometer and MODIS AODs yielded a correlation coefficient of 0.96. MODIS fine mode fraction over the Bay of Bengal is higher (0.71) when compared to the Arabian Sea value of 0.60. Ångström exponent (α) over the Bay of Bengal is higher at 1.12, indicating the dominance of smaller size aerosols in the aerosol columnar distribution than the Arabian Sea (0.73), while Ångström coefficient (β) is comparable at 0.15 and 0.16 for the Bay of Bengal and the Arabian Sea. Background AODs are higher over the Bay of Bengal and the Arabian Sea indicating a strong continental influence. The scaling distance is lower over the Bay of Bengal due to nearly similar AODs, while the scaling distance over the Arabian Sea is about 2000 km. The anthropogenic influence in AODs over the Bay of Bengal and the Arabian Sea estimated using wind speed dependent AODs and maritime clean AODs are found to agree within ±1σ of the anthropogenic fraction obtained from MODIS AODs and FMFs. The mean anthropogenic contribution to the AODs estimated from the three methods is higher over the Bay of Bengal (68-75%) than the Arabian Sea (51-65%).

  15. A Campaign Study of Sea Spray Aerosol Properties in the Bay of Aarhus

    NASA Astrophysics Data System (ADS)

    Nguyen, Quynh; Rasmussen, Berit; Kristensen, Kasper; Sloth Nielsen, Lærke; Bilde, Merete

    2016-04-01

    The oceans of the world are a dominant source of atmospheric aerosol. Together with mineral dust, sea spray aerosols (SSA) constitute the largest mass flux of particulate matter in the atmosphere (Andreae and Rosenfeld, 2008). Due to their effects on the global radiative budget - both directly as scatterers and absorbers of solar and terrestrial radiation, and indirectly as cloud condensation nuclei (CCN), SSA are considered an important component of the climate system. The sea-surface microlayer (SML) is an ultra-thin boundary layer between the ocean and the atmosphere. The high concentration of surface-active organic compounds in the SML, compared to that of the underlying water column, creates rigid film-like layer over the surface of the ocean. The SML is believed to play an important role in the formation and composition of SSA. However, current knowledge on the SML and its impacts on SSA remain limited. To characterize the SML of natural seawater and examine its impacts on aerosol properties, a field campaign was conducted in the bay of Aarhus, Denmark, during spring 2015. Bulk seawater was collected 1-2 times every week along with selective sampling of the SML. Characterization of the sea water and SML included a wide range of measurements, including surface tension, water activity, dissolved organic matter, and chemical composition analysis by liquid chromatography/electrospray ionization high-resolution quadrupole time-of-flight mass spectrometry (UPLC/ESI-HR-Q-TOFMS). SSA was generated from sampled sea water by diffusion of air bubbles through a 10L seawater sample situated in a sea spray tank. Particle number concentration and CCN measurements were conducted along with measurements of the organic share in the aerosol phase as indicated by volatility measurements. To investigate the effect of the SML, spiking of the seawater samples with additional SML was performed and measurements repeated for comparison. Preliminary results show that the SML samples

  16. Measuring the vertical distributions of the upper tropospheric and stratospheric dust with a LOAC aerosol counter under meteorological balloons

    NASA Astrophysics Data System (ADS)

    Vignelles, Damien; Renard, Jean-Baptiste; Berthet, Gwenael; Dulac, François; Coute, Benoit; Jeannot, Matthieu; Jegou, Fabrice; Olafsson, Haraldur; Dagsson Waldhauserova, Pavla

    2014-05-01

    The aerosol issue is in a constant growing. At ground, the airborne particles in boundary layer represent a real risk for population and must be control. In the middle troposphere, aerosols play an important role in the microphysics and meteorology, the heterogeneous chemistry is not well understood. In the stratosphere, several teams of researchers have shown that solid aerosols might exist, the question of the dynamic of these solid aerosol in the stratosphere is open. The aim was to develop an instrument that it can make measurements from the ground to the middle stratosphere. This instrument must be able to be put under meteorological balloons, which represent the worst conditions for the development of such instruments in terms of weight, resistance under large variations of temperature and pressure, autonomy and cost if we consider that something throw under a meteorological balloon can be lost after the fly. In the consideration of these conditions, we have developed a new instrument able to make such kind of measurements. This instrument is call LOAC for Light Optical Aerosol Counter. LOAC provides the concentration and size distribution of aerosols on 19 channels from 0.2 μm to 50.0 μm every ten seconds, and determine the main nature of particles (carbonaceous aerosol, mineral, droplets of water or sulfuric acid) in relation with a large range of samples in laboratory. The physical technique is based on the observation of the scattered light by particles at two angles. LOAC is light enough (1 kilogram) to be placed under a meteorological balloon that is very easy to launch such balloons. The goal is to perform a large number of flights to gather information about the dust distribution in stratosphere and to understand the various mechanisms controlling their spatial and temporal variability. About 25 flights with have been performed in the stratosphere with the LOAC above the Mediterranean Sea, from south of Paris, from Aire-Sur-l'Adour (South-West of

  17. Study of aerosol transport through precipitation chemistry over Arabian Sea during winter and summer monsoons

    NASA Astrophysics Data System (ADS)

    Praveen, P. S.; Rao, P. S. P.; Safai, P. D.; Devara, P. C. S.; Chate, D. M.; Ali, K.; Momin, G. A.

    Precipitation samples over the Arabian Sea collected during Arabian Sea Monsoon Experiment (ARMEX) in 2002-2003 were examined for major water soluble components and acidity of aerosols during the period of winter and summer monsoon seasons. The pH of rain water was alkaline during summer monsoon and acidic during winter monsoon. Summer monsoon precipitation showed dominance of sea-salt components (˜90%) and significant amounts of non-sea salt (nss) Ca 2+ and SO 42-. Winter monsoon precipitation samples showed higher concentration of NO 3- and NH 4+ compared to that of summer monsoon, indicating more influence of anthropogenic sources. The rain water data is interpreted in terms of long-range transport and background pollution. In summer monsoon, air masses passing over the north African and Gulf continents which may be carrying nss components are advected towards the observational location. Also, prevailing strong southwesterly winds at surface level produced sea-salt aerosols which led to high sea-salt contribution in precipitation. While in winter monsoon, it was observed that, air masses coming from Asian region towards observational location carry more pollutants like NO 3-and nss SO 42- that acidify the precipitation.

  18. A Numerical Study of Sea-Spray Aerosol Motion in a Coastal Thermal Internal Boundary Layer

    NASA Astrophysics Data System (ADS)

    Liang, Tinghao; Yu, Xiping

    2016-08-01

    A three-dimensional large-eddy simulation model is applied to the study of sea-spray aerosol transport, dispersion and settling in the coastal thermal internal boundary layer (IBL) formed by cool airflow from the open sea to the warm land. An idealized situation with constant inflow from the ocean and constant heat flux over the coastal land is considered. The numerical results confirm that the thickness of the coastal thermal IBL increases with the distance from the coastline until the outer edge of the IBL penetrates into the capping inversion layer. The thickness increases also with time until a fully-developed thermal boundary layer is formed. In addition, the thickness of the coastal thermal IBL increases more rapidly when the heat flux over the land is greater. Existence of large-scale eddies within the thermal IBL is identified and the turbulence intensity within the thermal IBL is also found to be significantly higher than that above. It is also indicated that the vertical position of the maximum concentration does not occur at the surface but increases as sea-spray aerosols are transported inland. The vertical position of the maximum flux of sea-spray aerosols within the coastal thermal IBL is shown to coincide with that of the maximum vertical velocity fluctuations when the coastal thermal IBL is fully developed with increased distance in the airflow direction.

  19. Evaluation of aerosol distributions in the GISS-TOMAS global aerosol microphysics model with remote sensing observations

    NASA Astrophysics Data System (ADS)

    Lee, Y. H.; Adams, P. J.

    2010-03-01

    The Aerosol Optical Depth (AOD) and Angstrom Coefficient (AC) predictions in the GISS-TOMAS model of global aerosol microphysics are evaluated against remote sensing data from MODIS, MISR, and AERONET. The model AOD agrees well (within a factor of two) over polluted continental (or high sulfate), dusty, and moderate sea-salt regions but less well over the equatorial, high sea-salt, and biomass burning regions. Underprediction of sea-salt in the equatorial region is likely due to GCM meteorology (low wind speeds and high precipitation). For the Southern Ocean, overprediction of AOD is very likely due to high sea-salt emissions and perhaps aerosol water uptake in the model. However, uncertainties in cloud screening at high latitudes make it difficult to evaluate the model AOD there with the satellite-based AOD. AOD in biomass burning regions is underpredicted, a tendency found in other global models but more severely here. Using measurements from the LBA-SMOCC 2002 campaign, the surface-level OC concentration in the model are found to be underpredicted severely during the dry season while much less severely for EC concentration, suggesting the low AOD in the model is due to underpredictions in OM mass. The potential for errors in emissions and wet deposition to contribute to this bias is discussed.

  20. 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.

  1. Theory of the Sea Ice Thickness Distribution

    NASA Astrophysics Data System (ADS)

    Toppaladoddi, Srikanth; Wettlaufer, J. S.

    2015-10-01

    We use concepts from statistical physics to transform the original evolution equation for the sea ice thickness distribution g (h ) from Thorndike et al. into a Fokker-Planck-like conservation law. The steady solution is g (h )=N (q )hqe-h /H, where q and H are expressible in terms of moments over the transition probabilities between thickness categories. The solution exhibits the functional form used in observational fits and shows that for h ≪1 , g (h ) is controlled by both thermodynamics and mechanics, whereas for h ≫1 only mechanics controls g (h ). Finally, we derive the underlying Langevin equation governing the dynamics of the ice thickness h , from which we predict the observed g (h ). The genericity of our approach provides a framework for studying the geophysical-scale structure of the ice pack using methods of broad relevance in statistical mechanics.

  2. Theory of the Sea Ice Thickness Distribution.

    PubMed

    Toppaladoddi, Srikanth; Wettlaufer, J S

    2015-10-01

    We use concepts from statistical physics to transform the original evolution equation for the sea ice thickness distribution g(h) from Thorndike et al. into a Fokker-Planck-like conservation law. The steady solution is g(h)=N(q)h(q)e(-h/H), where q and H are expressible in terms of moments over the transition probabilities between thickness categories. The solution exhibits the functional form used in observational fits and shows that for h≪1, g(h) is controlled by both thermodynamics and mechanics, whereas for h≫1 only mechanics controls g(h). Finally, we derive the underlying Langevin equation governing the dynamics of the ice thickness h, from which we predict the observed g(h). The genericity of our approach provides a framework for studying the geophysical-scale structure of the ice pack using methods of broad relevance in statistical mechanics. PMID:26551827

  3. Effect of In-Plume Aerosol Processing on the Efficacy of Marine Cloud Albedo Enhancement from Controlled Sea-Spray Injections

    NASA Astrophysics Data System (ADS)

    Stuart, G. S.; Stevens, R. G.; Spracklen, D. V.; Korhonen, H.; Pierce, J. R.

    2012-12-01

    The intentional enhancement of cloud albedo via controlled sea-spray injection from ships has been proposed as a possible method to control anthropogenic global warming (1); however, there remains significant uncertainty in the efficacy of this method due to uncertainties in aerosol and cloud microphysics. A major assumption used in multiple recent studies (2,3) is that all sea-spray was emitted uniformly into some oceanic grid boxes, and thus did not account for sub-grid aerosol microphysics within the sea-spray plumes. However, as a consequence of the fast sea-spray injection rates which are proposed, in the order of 10^17 1/s (1), particle concentrations in these plumes may be quite high and particle coagulation may significantly reduce the number of emitted particles and increase their average size. Therefore, it is possible that the emissions necessary to reach a desired cooling may be even larger than currently assumed. We explore the evolution of these sea-salt plumes using a multi-shelled Gaussian plume model with size-resolved aerosol coagulation. We determine how the final number and size of particles depends on the emission rate and size distribution of the emitted sea-spray plume and local atmospheric conditions, including wind speed and boundary-layer stability. Under the injection rates reported in (1) and typical marine conditions, we find that the number of aerosol particles is reduced by about 40%. This fraction decreases for decreasing emission rates or increasing wind speeds due to lower particle concentrations in the plume. Finally, we make suggestions for effective size-resolved emissions for use in climate models. (1) Salter, S. et al., Phil. Trans. R. Soc. A., 2008. (2) Korhonen, H. et al., Atmos. Chem. Phys., 10, 4133-4143, 2010. (3) Partanen, A.-I. et al., J. Geophys. Res., 117, D02203, 2012.

  4. Sensitivity of remote aerosol distributions to representation of cloud-aerosol interactions in a global climate model

    NASA Astrophysics Data System (ADS)

    Wang, H.; Easter, R. C.; Rasch, P. J.; Wang, M.; Liu, X.; Ghan, S. J.; Qian, Y.; Yoon, J.-H.; Ma, P.-L.; Velu, V.

    2013-01-01

    the Arctic winter (summer) BC burden. This BC aging treatment, however, has minimal effect on other under-predicted species. Interestingly, our modifications to CAM5 that aim at improving prediction of high-latitude and upper tropospheric aerosols also produce much better aerosol optical depth over various other regions globally when compared to multi-year AERONET retrievals. The improved aerosol distributions have impacts on other aspects of CAM5, improving the simulation of global mean liquid water path and cloud forcing.

  5. Dust and polluted aerosol impacts on diazotrophy during a mesocosm experiment in the Eastern Mediterranean Sea

    NASA Astrophysics Data System (ADS)

    Rahav, Eyal; Herut, Barak; Liu, Hongbin; Guo, Cui; Cheung, Isaac; Psarra, Stella; Lagaria, Anna; Tsiola, Anastasia; Tsagaraki, Tanya; Pitta, Paraskevi; Mulholland, Margaret; Berman-Frank, Ilana

    2014-05-01

    Atmospheric inputs of nutrients via dust and aerosols to the surface ocean layer are considered to contribute greatly to dinitrogen (N2) fixation and to primary productivity. N2 fixation rates in the Mediterranean Sea are typically low and the parameters limiting this process are still unclear. Addition of dust analogs to a mesocosm experiment in the Western Mediterranean Sea (DUNE) enhanced N2 fixation by 3 to 5 fold. However, in the Eastern Mediterranean Sea, an area highly exposed to Saharan dust and aerosol, the impact of these inputs on N2 fixation from onboard microcosm experiment are unclear and inconclusive. We examined the influence of Saharan dust (1.6 mg L-1) and polluted aerosol (1 mg L-1) additions on diazotroph populations and N2 fixation rates in nine 3 m3 mesocosms (MESOAQUA project) using the enriched seawater method of 15N uptake. The enrichments induced an immediate 2-4 fold increase in N2 fixation (measured from 6 to 48 h after enrichments). After 4 days, N2 fixation rates returned to their background level and no significant change was observed relative to the control mesocosms. The increase in N2 fixation rates were reflected in the differential composition of diazotrophs. Dust enrichment enhanced the abundance of the filamentous cyanobacterium Trichodesmium spp., while aerosol addition predominantly enhanced the presence of heterotrophic diazotrophs including Pseudomonas and Desulfovibrio. Our results indicate that sources of nutrients supplied via Saharan dust and polluted aerosol pulses to the stratified surface Eastern Mediterranean waters could increase the contribution of diazotrophs and N2 fixation in these ultraoligotrophic waters and impact productivity and biogeochemical cycling.

  6. Characterization of aerosol over the Northern South China Sea during two cruises in 2003

    NASA Astrophysics Data System (ADS)

    Zhang, Xingying; Zhuang, Guoshun; Guo, Jinghua; Yin, Kedong; Zhang, Peng

    Atmospheric transport of trace elements has been found to be an important pathway for their input to the ocean. TSP, PM10, and PM2.5 aerosol samples were collected over the Northern South China Sea in two cruises in 2003 to estimate the input of aerosol from continent to the ocean. About 23 elements and 14 soluble ions in aerosol samples were measured. The average mass concentration of TSP in Cruise I in January (78 μg m -3) was ˜twice of that in Cruise II in April (37 μg m -3). Together with the crustal component, heavy metals from pollution sources over the land (especially from the industry and automobiles in Guangzhou) were transported to and deposited into the ocean. The atmospheric MSA concentrations in PM2.5 (0.048 μg m -3 in Cruise I and 0.043 μg m -3 in Cruise II) over Northern South China Sea were comparable to those over other coastal regions. The ratio of non-sea-salt (NSS)-sulfate to MSA is 103-655 for Cruise I and 15-440 for Cruise II in PM2.5 samples, which were much higher than those over remote oceans. The estimated anthropogenic sulfate accounts for 83-98% in Cruise I and 63-95% in Cruise II of the total NSS-sulfate. Fe (II) concentration in the aerosols collected over the ocean ranged from 0.1 to 0.9 μg m -3, accounting for 16-82% of the total iron in the aerosol, which could affect the marine biogeochemical cycle greatly.

  7. Aerosol Size Distribution, Composition, and Hygroscopicity Measurements During CSTRIPE Using an Aerosol Mass Spectrometer and a Dual Differential Mobility Analyzer

    NASA Astrophysics Data System (ADS)

    Bahreini, R.; Varutbangkul, V.; Conant, W. C.; Flagan, R. C.; Seinfeld, J. H.; Buzorius, G.; Jonsson, H. H.

    2003-12-01

    During July 2003, the CIRPAS Twin Otter aircraft was deployed in the CSTRIPE (Coastal STRatocumulus Imposed Perturbation Experiment) field experiment in order to quantify the effects of aerosols on the microphysics and dynamics of marine stratocumulus clouds. In order to characterize the effects of different aerosol types on stratocumulus clouds, various air masses were sampled, including local fire plumes, pollution over the San Joaquin valley, unperturbed marine stratocumulus clouds, and stratocumulus clouds perturbed by seeding flares. Some research flights were also dedicated to characterize the seeding flares in the clear sky. Measurements of aerosol mass distribution and composition, using an Aerodyne Aerosol Mass Spectrometer (AMS), and size distribution and hygroscopic behavior, using a Dual Differential Mobility Analyzer (Dual DMA) with one column at dry conditions and another at a relative humidity of approximately 70 percent, will be presented here. During a number of in-cloud sampling periods, the Counter-flow Virtual Impactor (CVI) was used to select and dry cloud droplets, which were then analyzed by the AMS and the Dual DMA. The AMS composition measurements showed that sulfate and organics comprised most of the mass of the non-refractory components of the aerosol. The DMA showed a mixture of unimodal and bimodal size distributions in most types of air masses. The air mass over the San Joaquin valley, however, showed strong evidence of freshly nucleated particles, with aerosol number concentrations often above 80,000 cm-3.

  8. Organic Composition and Morphology of Sea Spray Aerosols as a Function of Biological Life during IMPACTS

    NASA Astrophysics Data System (ADS)

    Pham, D.; Moffet, R.; Fraund, M. W.; O'Brien, R.; Laskina, O.; Prather, K. A.; Grassian, V. H.; Beall, C.; Wang, X.; Forestieri, S.; Cappa, C. D.

    2015-12-01

    Aerosols influence climate by directly reflecting or absorbing sunlight, or indirectly by affecting clouds. A major source of aerosols is from oceanic wave breaking. Due to their complexity, the effects of marine aerosol on climate are uncertain. To provide more detailed measurements of the chemical composition of marine aerosols, Scanning Transmission X-Ray Microscopy coupled with Near Edge X-Ray Absorption Fine Structure (SXTM-NEXAFS) was used to give spatially resolved molecular information for carbon and oxygen. Application of STXM/NEXAFS to particles collected during a mesocosm study using a unique wave channel facility to generate aerosols shows that the organic volume fraction of aerosols at the aerodynamic diameter size range of 0.18-0.32 μm are a direct function of the biological activity in the sea water. Aerosol organic volume fraction increased from 0.32 for particles generated from seawater containing low biolife to 0.49 and 0.40 for particles produced during phytoplankton blooms. However, the organic volume fraction of aerosols at the aerodynamic diameter size range of 0.56-1 μm did not change with biological activity. Measurements also show that different types of organics can concentrate into aerosols depending on the enzyme activity expressed at the time. Enhanced spectral signatures for aliphatic hydrocarbons were observed during the first phytoplankton bloom compared to a second phytoplankton bloom occurring directly thereafter. The decreased signature of aliphatic organics in the second phytoplankton bloom was correlated with increased lipase activity from heterobacteria. Organic aggregates having similar morphology also differ in composition from their carbon spectra from the two blooms. For July 17, organic aggregates were much richer in hydrocarbons, which showed a remarkably intense C-H absorbance and a broad C-C absorbance. Organic aggregates observed for July 26-27, did not have the C-H and C-C signatures, but contained more polar

  9. Role of sea ice and hemispheric circulation mode on sulphur oxidised compounds (Methanesulfonate and Sulfate) in the Artic aerosol

    NASA Astrophysics Data System (ADS)

    Becagli, Silvia; Calzolai, Giulia; Dayan, Uri; Di Biagio, Claudia; di Sarra, Alcide; Frosini, Daniele; Mazzola, Mauro; Rugi, Francesco; Severi, Mirko; Traversi, Rita; Vitale, Vito; Udisti, Roberto

    2013-04-01

    The recent decline in sea ice cover in the Arctic Ocean is expected to affect the regional radiation budget and to influence the ocean-atmosphere exchange of dimethylsulfide (DMS), thus the amount of biogenic aerosols formed from its atmospheric oxidation, such as methanesulfonate (MS-) and non-sea salt sulphate (nssSO42-). This study examines the temporal evolution of atmospheric MS- and nssSO42-, as measured in atmospheric aerosols, at Ny-Ålesund, (78.9°N, 11.9°E, Svalbard islands) and Thule (76.5°N, 68.8°W, Greenland) during three years (2010-12). Aerosol sampling was carried out using a PM10 sampler with Teflon filters, and a 12-stage impactor (SDI, Small Deposit-area Impactor) with polycarbonate filters. Analyses were performed by ion chromatography, for ion composition, and ICP-SFMS, for selected metals; both techniques are sufficiently sensitive, accurate, and reproducible to be applied to very low atmospheric load of aerosol particles, typical of remote polar regions. The evolution of MS- and nssSO4 concentrations was analysed as a function of speciation (as acidic species or ammonium salt), size distribution, and airmass pathways. This study reveals that nssSO4 is meanly associated with long range transport from anthropic sources, and presents a relative maximum in spring. Conversely, MS- arises from natural local sources and shows a peak in mid-summer. A large interannual variability is observed in MS- concentration with values in spring-summer 2010 in both the stations higher than in the other summers. In the previous winter a larger sea ice extent and larger sea ice melting surface in the following spring were observed. Arrigo et al. (2008) have observed a 22% increase in the annual primary productivity, that has been attributed to a longer phytoplankton growing season connected with the progressive decline in sea ice coverage in the Arctic over the past decade. Modeling results (Gabric et al., 2005) suggest that an increase in DMS production would

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

    PubMed

    Yue, G K

    2000-10-20

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

  11. A diagnostic stratospheric aerosol size distribution inferred from SAGE II measurements

    NASA Technical Reports Server (NTRS)

    Thomason, Larry W.

    1991-01-01

    An aerosol size distribution model for the stratosphere is inferred based on 5 years of Stratospheric Aerosol and Gas Experiment (SAGE) II measurements of multispectral aerosol and water vapor extinction. The SAGE II aerosol and water vapor extinction data strongly suggest that there is a critical particle radius below which there is a relatively weak dependence of particle number density with size and above which there are few, if any, particles. A segmented power law model, as a simple representation of this dependence, is used in theoretical calculations and intercomparisons with a variety of aerosol measurements including dustsondes, longwave lidar, and wire impactors and shows a consistently good agreement.

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

    NASA Astrophysics Data System (ADS)

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

    2016-04-01

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

  13. Evidence for ships emissions in the Central Mediterranean Sea from aerosol chemical analyses at the island of Lampedusa

    NASA Astrophysics Data System (ADS)

    Becagli, S.; Sferlazzo, D. M.; Pace, G.; di Sarra, A.; Bommarito, C.; Calzolai, G.; Ghedini, C.; Lucarelli, F.; Meloni, D.; Monteleone, F.; Severi, M.; Traversi, R.; Udisti, R.

    2011-11-01

    Measurements of aerosol chemical composition made on the island of Lampedusa, south of the Sicily channel, during years 2004-2008, are used to identify the influence of ship emissions on aerosol particles in the Central Mediterranean. Evidence of ship emissions influence is found in 17% of the daily samples. Aerosol samples influenced by ships are characterized by elevated Ni and V soluble fraction (about 80% for aerosol from ships, versus about 40 % for crustal particles), high V and Ni to Si ratios, and values of Vsol>6 ng m-3. Back trajectories analysis on the selected events show that air masses prevalently come from the Sicily channel, where an intense ship traffic occurs. Vsol, Nisol, and non-sea salt SO42- (nssSO42-) show a marked seasonal behaviour, with an evident summer maximum. Such a pattern can be explained by several processes: (i) increased photochemical activity in summer, leading to a faster production of secondary aerosols, mainly nssSO42-, from the oxidation of SO2 in the ship plume; (ii) stronger marine boundary layer (MBL) stability in summer, leading to higher concentration of emitted compounds in the lowest atmospheric layers; (iii) more frequent meteorological conditions leading to consecutive days with trajectories from the Sicily channel in summer. A very intense event in spring 2008 was studied in detail, also using size segregated chemical measurements. These data show that elements arising from heavy oil combustion (V, Ni, Al, Fe) are distributed in the sub-micrometric fraction of the aerosol, and the metals are present as free metals, carbonates, oxides hydrates or labile complex with organic ligands, so that they are dissolved in mild condition (HNO3, pH1.5). Data suggest a characteristic nssSO42-/V ratio in the range 200-400 for ship emission aerosols in summer at Lampedusa. By using the value of 200 a lower limit for the ship contribution to total sulphates is estimated. Ship emissions account, as a summer average, at least for 1

  14. Are atmospheric aerosols able to modify the surface winds? A sensitivity study of the biomass burning aerosols impact on the spatially-distributed wind over Europe

    NASA Astrophysics Data System (ADS)

    Baró, Rocío; Lorente-Plazas, Raquel; Jerez, Sonia; Montávez, Juan Pedro; Jiménez-Guerrero, Pedro

    2015-04-01

    Atmospheric aerosols affect the Earth's climate through their radiative effects, being one of the most uncertain areas in climate modelling. Aerosols are widely known to affect radiation, temperature, stability, clouds and precipitation through their radiative effects, which depend mainly on the aerosol optical properties. These can be divided into direct and semi-direct effect, produced by the scattering and absorption of radiation; and indirect effect, which influences the aerosols-cloud interactions. In this sense, wind fields affect aerosols levels by several different processes, finally resulting in a wind-dependent emission over land or ocean. Moreover they can disperse the particles leading to a cleaner atmosphere. But, how do aerosol particles affect the wind? Scientific literature about their effects on wind is scarce. In this sense, the objective of this work is to assess the effects of biomass burning aerosols on spatially-distributed winds over Europe. The methodology carried out consists of three WRF-Chem simulations for Europe during the Russian fires (25 July to 15 August 2010) differing in the inclusion (or not) of aerosol direct and direct+indirect radiative feedbacks. These simulations have been carried out under the umbrella of the EuMetChem COST ES1004 Action. A Euro-CORDEX compliant domain at 0.22° and 23 km resolution has been used. The first simulation does not take into account any aerosol feedbacks (NFB), the second simulation differs from the base case by the inclusion of direct effect (DFB); while the third includes the direct+indirect radiative feedbacks (TFB). Results depict that the presence of aerosol reduces the wind module over Russian. Aerosol radiative effects imply a decrease of the shortwave downwelling radiation at the bottom of the atmosphere (with maximum values of 50 W m-2 over Russia). As a consequence there is a reduction on the temperature at 2 m up to 1 K. The decrease of the temperature reduces the convective processes

  15. Comparative analysis of aerosols elemental distribution in some Romanian regions

    NASA Astrophysics Data System (ADS)

    Amemiya, Susumu; Masuda, Toshio; Popa-Simil, Liviu; Mateescu, Liviu

    1996-04-01

    The study's main aim is obtaining aerosols particulate elemental distribution and mapping it for some Romanian regions, in order to obtain preliminary information regarding the concentrations of aerosol particles and networking strategy versus local conditions. For this we used the mobile sampling strategy, but taking care on all local specific conditions and weather. In the summer of 1993, in July we took about 8 samples on a rather large territory of SE Romania which were analysed and mapped. The regions which showed an interesting behaviour or doubts such as Bucharest and Dobrogea were zoomed in near the same period of 1994, for comparing the new details with the global aspect previously obtained. An attempt was made to infer the minimum necessary number of stations in a future monitoring network. A mobile sampler was used, having tow polycarbonate filter posts of 8 and 0.4 μm. PIXE elemental analysis was performed on a 2.5 MV Van de Graaff accelerator, by using a proton beam. More than 15 elements were measured. Suggestive 2D and 3D representations were drawn, as well as histogram charts for the concentrations' distribution in the specific regions at the specified times. In spite of the poor samples from the qualitative point of view the experiment surprised us by the good coincidence (good agreement) with realities in terrain known by other means long time ago, and highlighted the power of PIXE methods in terms of money and time. Conclusions over the link between industry, traffic, vegetation, wether, surface waters, soil composition, power plant exhaust and so on, on the one hand, and surface concentration distribution, on the other, were drawn. But the method's weak points were also highlighted; these are weather dependencies (especially air masses movement and precipitation), local relief, microclimate and vegetation, and of course localisation of the sampling point versus the pollution sources and their regime. The paper contains a synthesis of the whole

  16. Heterogeneous Reactivity of Nitric Acid with Nascent Sea Spray Aerosol: Large Differences Observed between and within Individual Particles.

    PubMed

    Ault, Andrew P; Guasco, Timothy L; Baltrusaitis, Jonas; Ryder, Olivia S; Trueblood, Jonathan V; Collins, Douglas B; Ruppel, Matthew J; Cuadra-Rodriguez, Luis A; Prather, Kimberly A; Grassian, Vicki H

    2014-08-01

    Current climate and atmospheric chemistry models assume that all sea spray particles react as if they are pure NaCl. However, recent studies of sea spray aerosol particles have shown that distinct particle types exist (including sea salt, organic carbon, and biological particles) as well as mixtures of these and, within each particle type, there is a range of single-particle chemical compositions. Because of these differences, individual particles should display a range of reactivities with trace atmospheric gases. Herein, to address this, we study the composition of individual sea spray aerosol particles after heterogeneous reaction with nitric acid. As expected, a replacement reaction of chloride with nitrate is observed; however, there is a large range of reactivities spanning from no reaction to complete reaction between and within individual sea spray aerosol particles. These data clearly support the need for laboratory studies of individual, environmentally relevant particles to improve our fundamental understanding as to the properties that determine reactivity.

  17. Integrating biomass, sulphate and sea-salt aerosol responses into a microphysical chemical parcel model: implications for climate studies.

    PubMed

    Ghosh, S; Smith, M H; Rap, A

    2007-11-15

    Aerosols are known to influence significantly the radiative budget of the Earth. Although the direct effect (whereby aerosols scatter and absorb solar and thermal infrared radiation) has a large perturbing influence on the radiation budget, the indirect effect (whereby aerosols modify the microphysical and hence the radiative properties and amounts of clouds) poses a greater challenge to climate modellers. This is because aerosols undergo chemical and physical changes while in the atmosphere, notably within clouds, and are removed largely by precipitation. The way in which aerosols are processed by clouds depends on the type, abundance and the mixing state of the aerosols concerned. A parametrization with sulphate and sea-salt aerosol has been successfully integrated within the Hadley Centre general circulation model (GCM). The results of this combined parametrization indicate a significantly reduced role, compared with previous estimates, for sulphate aerosol in cloud droplet nucleation and, consequently, in indirect radiative forcing. However, in this bicomponent system, the cloud droplet number concentration, N(d) (a crucial parameter that is used in GCMs for radiative transfer calculations), is a smoothly varying function of the sulphate aerosol loading. Apart from sea-salt and sulphate aerosol particles, biomass aerosol particles are also present widely in the troposphere. We find that biomass smoke can significantly perturb the activation and growth of both sulphate and sea-salt particles. For a fixed salt loading, N(d) increases linearly with modest increases in sulphate and smoke masses, but significant nonlinearities are observed at higher non-sea-salt mass loadings. This non-intuitive N(d) variation poses a fresh challenge to climate modellers.

  18. Estimation of aerosol columnar size distribution and optical thickness from the angular distribution of radiance exiting the atmosphere: simulations.

    PubMed

    Wang, M; Gordon, H R

    1995-10-20

    We report the results of simulations in which an algorithm developed for estimation of aerosol optical properties from the angular distribution of radiance exiting the top of the atmosphere over the oceans [Appl. Opt. 33, 4042 (1994)] is combined with a technique for carrying out radiative transfer computations by synthesis of the radiance produced by individual components of the aerosol-size distribution [Appl. Opt. 33, 7088 (1994)], to estimate the aerosol-size distribution by retrieval of the total aerosol optical thickness and the mixing ratios for a set of candidate component aerosol-size distributions. The simulations suggest that in situations in which the true size-refractive-index distribution can actually be synthesized from a combination of the candidate components, excellent retrievals of the aerosol optical thickness and the component mixing ratios are possible. An exception is the presence of strongly absorbing aerosols. The angular distribution of radiance in a single spectral band does not appear to contain sufficient information to separate weakly from strongly absorbing aerosols. However, when two spectral bands are used in the algorithm, retrievals in the case of strongly absorbing aerosols are improved. When pseudodata were simulated with an aerosol-size distribution that differed in functional form from the candidate components, excellent retrievals were still obtained as long as the refractive indices of the actual aerosol model and the candidate components were similar. This underscores the importance of component candidates having realistic indices of refraction in the various size ranges for application of the method. The examples presented all focus on the multiangle imaging spectroradiometer; however, the results should be as valid for data obtained by the use of high-altitude airborne sensors. PMID:21060560

  19. Meridional gradients in aerosol vertical distribution over Indian Mainland: Observations and model simulations

    NASA Astrophysics Data System (ADS)

    Prijith, S. S.; Suresh Babu, S.; Lakshmi, N. B.; Satheesh, S. K.; Krishna Moorthy, K.

    2016-01-01

    Multi-year observations from the network of ground-based observatories (ARFINET), established under the project 'Aerosol Radiative Forcing over India' (ARFI) of Indian Space Research Organization and space-borne lidar 'Cloud Aerosol Lidar with Orthogonal Polarization' (CALIOP) along with simulations from the chemical transport model 'Goddard Chemistry Aerosol Radiation and Transport' (GOCART), are used to characterize the vertical distribution of atmospheric aerosols over the Indian landmass and its spatial structure. While the vertical distribution of aerosol extinction showed higher values close to the surface followed by a gradual decrease at increasing altitudes, a strong meridional increase is observed in the vertical spread of aerosols across the Indian region in all seasons. It emerges that the strong thermal convections cause deepening of the atmospheric boundary layer, which although reduces the aerosol concentration at lower altitudes, enhances the concentration at higher elevations by pumping up more aerosols from below and also helping the lofted particles to reach higher levels in the atmosphere. Aerosol depolarization ratios derived from CALIPSO as well as the GOCART simulations indicate the dominance of mineral dust aerosols during spring and summer and anthropogenic aerosols in winter. During summer monsoon, though heavy rainfall associated with the Indian monsoon removes large amounts of aerosols, the prevailing southwesterly winds advect more marine aerosols over to landmass (from the adjoining oceans) leading to increase in aerosol loading at lower altitudes than in spring. During spring and summer months, aerosol loading is found to be significant, even at altitudes as high as 4 km, and this is proposed to have significant impacts on the regional climate systems such as Indian monsoon.

  20. Atmospheric aerosol impacts on sea surface temperatures and medium range forecast.

    NASA Astrophysics Data System (ADS)

    Oyola, M. I.; Joseph, E.; Lu, C. H.; Nalli, N. R.

    2014-12-01

    This work proposes a series of experiments to analyze the impact of dust aerosols on numerical weather prediction (NWP) and the global data assimilation system. We strive to accomplish this by the application of the NOAA Environmental Modeling System/Global Forecasting System (NEMS/GFS) aerosol component (NGAC), which corresponds to the first global interactive atmosphere-aerosol forecast system ever implemented at NOAA's National Center for Environmental Prediction (NCEP) and which has been operational since September 2012. Specifically, our approach will include the implementation of an improved satellite sea surface temperature (SST) retrieval methodology, that allows for better representation of the atmospheric state under dust-laden conditions. Specifically, the new algorithm will be included within the NGAC aerosol product to improve the accuracy of the SST analysis and examine the impact on NWP, particularly in tropical cyclone genesis regions in the eastern Atlantic. The results of these corrections are validated against observed measurements from the eastern Atlantic Ocean, which is dominated by Saharan dust throughout most of the year and that is also a genesis region for Atlantic tropical cyclones. These observations are obtained from the NOAA Aerosols and Ocean Science Expeditions (AEROSE) and PIRATA Northeast Extension (PNE) buoys network. We believe that the improved physical SST methodology has the potential to allow for improved representation of the geophysical state under dust-laden conditions

  1. Sensitivity of Remote Aerosol Distributions to Representation of Cloud-Aerosol Interactions in a Global Climate Model

    SciTech Connect

    Wang, Hailong; Easter, Richard C.; Rasch, Philip J.; Wang, Minghuai; Liu, Xiaohong; Ghan, Steven J.; Qian, Yun; Yoon, Jin-Ho; Ma, Po-Lun; Vinoj, V.

    2013-06-05

    the Arctic winter (summer) BC burden. This BC aging treatment, however, has minimal effect on other under-predicted species. Interestingly, our modifications to CAM5 that aim at improving prediction of high-latitude and upper tropospheric aerosols also produce much better AOD and AAOD over various other regions globally when compared to multi-year AERONET retrievals. The improved aerosol distributions have impacts on other aspects of CAM5, improving the simulation of global mean liquid water path and cloud forcing.

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

    NASA Astrophysics Data System (ADS)

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

    2009-12-01

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

  3. Analysis of aerosol distribution inside the object "shelter" at the Chernobyl nuclear reactor site.

    PubMed

    Bondarenko, O A; Aryasov, P B; Melnichuk, D V; Medvedev, S Y

    2001-08-01

    Results of the aerosol sampling inside the Object Shelter at the Chornobyl nuclear reactor site are considered in the work. The results show a consistent and significant contribution of submicron fraction to the total aerosol activity. Different methods of interpretation of impactor data series are compared in order to indicate and detect in the most effective way the submicron fraction as a separate component of the distribution. The methods used are as follows-method of probabilistic-logarithmic scale, method of likelihood function, non-linear approximation by sum of several log-normal distributions, and restoration of the initial distribution using passage functions of impactor cascades. Practically all the collected data on aerosol distribution inside the Shelter show a distinct submicron component. The contribution of the submicron component into the total aerosol activity is about 35%. Influence of the actual aerosol distribution on the dose coefficients is analyzed.

  4. Sea spray aerosol in the Great Barrier Reef and the presence of nonvolatile organics

    NASA Astrophysics Data System (ADS)

    Mallet, Marc; Cravigan, Luke; Miljevic, Branka; Vaattovaara, Petri; Deschaseaux, Elisabeth; Swan, Hilton; Jones, Graham; Ristovski, Zoran

    2016-06-01

    Sea spray aerosol (SSA) particles produced from the ocean surface in regions of biological activity can vary greatly in size, number and composition, and in their influence on cloud formation. Algal species such as phytoplankton can alter the SSA composition. Numerous studies have investigated nascent SSA properties, but all of these have focused on aerosol particles produced by seawater from noncoral related phytoplankton and in coastal regions. Bubble chamber experiments were performed with seawater samples taken from the reef flat around Heron Island in the Great Barrier Reef during winter 2011. Here we show that the SSA from these samples was composed of an internal mixture of varying fractions of sea salt, semivolatile organics, as well as nonvolatile (below 550°C) organics. A relatively constant volume fraction of semivolatile organics of 10%-13% was observed, while nonvolatile organic volume fractions varied from 29% to 49% for 60 nm SSA. SSA organic fractions were estimated to reduce the activation ratios of SSA to cloud condensation nuclei by up to 14% when compared with artificial sea salt. Additionally, a sea-salt calibration was applied so that a compact time-of-flight aerosol mass spectrometer could be used to quantify the contribution of sea salt to submicron SSA, which yielded organic volume fractions of 3%-6%. Overall, these results indicate a high fraction of organics associated with wintertime Aitken mode SSA generated from Great Barrier Reef seawater. Further work is required to fully distinguish any differences coral reefs have on SSA composition when compared to open oceans.

  5. Aerosol size distribution and radiative forcing response to anthropogenically driven historical changes in biogenic secondary organic aerosol formation

    NASA Astrophysics Data System (ADS)

    D'Andrea, S. D.; Acosta Navarro, J. C.; Farina, S. C.; Scott, C. E.; Rap, A.; Farmer, D. K.; Spracklen, D. V.; Riipinen, I.; Pierce, J. R.

    2015-03-01

    Emissions of biogenic volatile organic compounds (BVOCs) have changed in the past millennium due to changes in land use, temperature, and CO2 concentrations. Recent reconstructions of BVOC emissions have predicted that global isoprene emissions have decreased, while monoterpene and sesquiterpene emissions have increased; however, all three show regional variability due to competition between the various influencing factors. In this work, we use two modeled estimates of BVOC emissions from the years 1000 to 2000 to test the effect of anthropogenic changes to BVOC emissions on secondary organic aerosol (SOA) formation, global aerosol size distributions, and radiative effects using the GEOS-Chem-TOMAS (Goddard Earth Observing System; TwO-Moment Aerosol Sectional) global aerosol microphysics model. With anthropogenic emissions (e.g., SO2, NOx, primary aerosols) turned off and BVOC emissions changed from year 1000 to year 2000 values, decreases in the number concentration of particles of size Dp > 80 nm (N80) of > 25% in year 2000 relative to year 1000 were predicted in regions with extensive land-use changes since year 1000 which led to regional increases in the combined aerosol radiative effect (direct and indirect) of > 0.5 W m-2 in these regions. We test the sensitivity of our results to BVOC emissions inventory, SOA yields, and the presence of anthropogenic emissions; however, the qualitative response of the model to historic BVOC changes remains the same in all cases. Accounting for these uncertainties, we estimate millennial changes in BVOC emissions cause a global mean direct effect of between +0.022 and +0.163 W m-2 and the global mean cloud-albedo aerosol indirect effect of between -0.008 and -0.056 W m-2. This change in aerosols, and the associated radiative forcing, could be a largely overlooked and important anthropogenic aerosol effect on regional climates.

  6. The impact of marine surface organic enrichment on the measured hygroscopicity parameter of laboratory generated sea-spray aerosols

    NASA Astrophysics Data System (ADS)

    Schill, S.; Novak, G.; Zimmermann, K.; Bertram, T. H.

    2014-12-01

    The ocean serves as a major source for atmospheric aerosol particles, yet the chemicophysical properties of sea spray aerosol to date are not well characterized. Understanding the transfer of organic compounds, present in the sea surface microlayer (SSML), to sea-spray particles and their resulting impact on cloud formation is important for predicting aerosol impact on climate in remote marine environments. Here, we present a series of laboratory experiments designed to probe the fractionation of select organic molecules during wave breaking. We use a representative set of organic mimics (e.g. sterols, sugars, lipids, proteins, fatty acids) to test a recent physically based model of organic enrichment in sea-spray aerosol [Burrows et al., 2014] that is based on Langmuir absorption equilibria. Experiments were conducted in the UCSD Marine Aerosol Reference Tank (MART) permitting accurate representation of wave breaking processes in the laboratory. We report kappa values for the resulting sea-spray aerosols and compare them to a predictions made using Kappa-Köhler Theory driven by a linear combination of the pure component kappa values. Hygroscopicity determinations made using the model systems are discussed within the context of measurements of CCN activity made using natural, coastal water.

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

    NASA Technical Reports Server (NTRS)

    Petrenko, Maksym; Ichoku, Charles

    2012-01-01

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

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

    NASA Technical Reports Server (NTRS)

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

    1994-01-01

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

  9. Ozone and aerosol distributions in the summertime troposphere over Canada

    NASA Technical Reports Server (NTRS)

    Browell, E. V.; Fenn, M. A.; Butler, C. F.; Grant, W. B.; Harriss, R. C.; Shipham, M. C.

    1994-01-01

    Measurements of ozone (O3) and aerosol distributions were made with an airborne lidar system in the lowland and boreal forest regions of eastern Canada during July - August 1990 as part of the NASA Global Tropospheric Experiment/Arctic Boundary Layer Expedition (ABLE) 3B. Aerosol and O3 profiles were measured simultaneously above and below the Electra aircraft from near the surface to above the tropopause on long-range flights over these important ecosystems. A broad range of atmospheric conditions were encountered during repeated flights over intensive study sites in the Hudson Bay lowlands near Moosonee, Ontario, and over the boreal forest near Schefferville, Quebec. The tropospheric composition in this high-latitude region was found to be strongly influenced by stratospheric intrusions. Regions of low aerosol scattering and enhanced O3 mixing ratios were correlated with descending air from the lower stratosphere. Over 33% of the troposphere (0-12 km) along our flight track at latitudes from about 45 deg to 55 deg N had significantly enhanced O3 due to stratospheric intrusions, and in the middle to upper troposphere the extent of the enhanced O3 gnerally exceeded 40%. Ozone mixing ratios of 80 parts per billion by volume (ppbv) near 6 km were common in strong intrusions. In the boundary layer over the lowlands, O3 was in the 20-30 ppbv range with a vertical O3 gradient of 6.7 ppbv/km to about 45 ppbv at 3 km. Above 6 km the background tropospheric O3 profile was nearly constant with an average value of 53 ppbv. Due to forest fires in Canada and Alaska, plumes from biomass-burning sources were observed on many flights. Biomass-burning plumes influenced about 25% of the free troposphere below 4 km, and in some of the plumes, O3 was enhanced by 10-20 ppbv over ambient levels of 30-45 ppbv. Several air masses transported from the tropical Pacific were observed over Canada in the middle to upper troposphere with O3 levels 10-20 ppbv below background values of 50

  10. Characterizing the Vertical Distribution of Aerosols Over the ARM SGP Site

    SciTech Connect

    Richard Ferrare, Connor Flynn, David Turner

    2009-05-05

    This project focused on: 1) evaluating the performance of the DOE ARM SGP Raman lidar system in measuring profiles of water vapor and aerosols, and 2) the use of the Raman lidar measurements of aerosol and water vapor profiles for assessing the vertical distribution of aerosols and water vapor simulated by global transport models and examining diurnal variability of aerosols and water vapor. The highest aerosol extinction was generally observed close to the surface during the nighttime just prior to sunrise. The high values of aerosol extinction are most likely associated with increased scattering by hygroscopic aerosols, since the corresponding average relative humidity values were above 70%. After sunrise, relative humidity and aerosol extinction below 500 m decreased with the growth in the daytime convective boundary layer. The largest aerosol extinction for altitudes above 1 km occurred during the early afternoon most likely as a result of the increase in relative humidity. The water vapor mixing ratio profiles generally showed smaller variations with altitude between day and night. We also compared simultaneous measurements of relative humidity, aerosol extinction, and aerosol optical thickness derived from the ARM SGP Raman lidar and in situ instruments on board a small aircraft flown routinely over the ARM SGP site. In contrast, the differences between the CARL and IAP aerosol extinction measurements are considerably larger. Aerosol extinction derived from the IAP measurements is, on average, about 30-40% less than values derived from the Raman lidar. The reasons for this difference are not clear, but may be related to the corrections for supermicron scattering and relative humidity that were applied to the IAP data. The investigators on this project helped to set up a major field mission (2003 Aerosol IOP) over the DOE ARM SGP site. One of the goals of the mission was to further evaluate the aerosol and water vapor retrievals from this lidar system

  11. Remote Sensing of Wind Fields and Aerosol Distribution with Airborne Scanning Doppler Lidar

    NASA Technical Reports Server (NTRS)

    Rothermel, Jeffry; Cutten, Dean R.; Johnson, Steven C.; Jazembski, Maurice; Arnold, James E. (Technical Monitor)

    2001-01-01

    The coherent Doppler laser radar (lidar), when operated from an airborne platform, is a unique tool for the study of atmospheric and surface processes and features. This is especially true for scientific objectives requiring measurements in optically-clear air, where other remote sensing technologies such as Doppler radar are typically at a disadvantage. The atmospheric lidar remote sensing groups of several US institutions, led by Marshall Space Flight Center, have developed an airborne coherent Doppler lidar capable of mapping the wind field and aerosol structure in three dimensions. The instrument consists of an eye-safe approx. 1 Joule/pulse lidar transceiver, telescope, scanner, inertial measurement unit, and flight computer system to orchestrate all subsystem functions and tasks. The scanner is capable of directing the expanded lidar beam in a variety of ways, in order to extract vertically-resolved wind fields. Horizontal resolution is approx. 1 km; vertical resolution is even finer. Winds are obtained by measuring backscattered, Doppler-shifted laser radiation from naturally-occurring aerosol particles (of order 1 micron diameter). Measurement coverage depends on aerosol spatial distribution and composition. Velocity accuracy has been verified to be approx. 1 meter per second. A variety of applications have been demonstrated during the three flight campaigns conducted during 1995-1998. Examples will be shown during the presentation. In 1995, boundary layer winds over the ocean were mapped with unprecedented resolution. In 1996, unique measurements were made of. flow over the complex terrain of the Aleutian Islands; interaction of the marine boundary layer jet with the California coastal mountain range; a weak dry line in Texas - New Mexico; the angular dependence of sea surface scattering; and in-flight radiometric calibration using the surface of White Sands National Monument. In 1998, the first measurements of eyewall and boundary layer winds within a

  12. Remote Sensing of Wind Fields and Aerosol Distributions with Airborne Scanning Doppler Lidar

    NASA Technical Reports Server (NTRS)

    Rothermel, Jeffry; Cutten, Dean R.; Goodman, H. Michael (Technical Monitor)

    2000-01-01

    The coherent Doppler lidar, when operated from an airborne platform, offers a unique measurement capability for study of atmospheric and surface processes and feature. This is especially true for scientific objectives requiring measurements in optically-clear air, where other remote sensing technologies such as Doppler radar are at a disadvantage in terms of spatial resolution and coverage. The atmospheric lidar remote sensing groups of several US institutions, led by Marshall Space Flight Center, have developed an airborne coherent Doppler lidar capable of mapping the wind field and aerosol structure in three dimensions. The instrument consists of about a 1 Joule/pulse (eyesafe) lidar transceiver, telescope, scanner, inertial measurement unit, and operations control system to orchestrate all subsystem functions and tasks. The scanner is capable of directing the expanded lidar beam in a variety of ways, in order to extract vertically resolved wind fields. Horizontal resolution is about 1 km; vertical resolution is even finer. Winds are obtained by measuring backscattered, Doppler-shifted laser radiation from naturally-occurring aerosol particles (on an order of 1 micron in diameter). Measurement coverage depends on aerosol spatial distribution and concentration. Velocity accuracy has been verified to be about 1 m/s. A variety of applications has been demonstrated during the three flight campaigns conducted during 1995-1998. Examples will be shown during the presentation. In 1995, boundary layer winds over the ocean were mapped with unprecedented resolution. In 1996, unique measurements were made of flow over the complex terrain of the Aleutian Islands; interaction of the marine boundary layer jet with the California coastal mountain range; a weak dry line in Texas - New Mexico; an upper tropospheric jet stream; the angular dependence of sea surface scattering; and in-flight radiometric calibration using the surface of White Sands National Monument. In 1998, the

  13. Ozone and aerosol distributions measured by airborne lidar during the 1988 Arctic Boundary Layer Experiment

    NASA Technical Reports Server (NTRS)

    Browell, Edward V.; Butler, Carolyn F.; Kooi, Susan A.

    1991-01-01

    Consideration is given to O3 and aerosol distributions measured from an aircraft using a DIAL system in order to study the sources and sinks of gases and aerosols over the tundra regions of Alaska during summer 1988. The tropospheric O3 budget over the Arctic was found to be strongly influenced by stratospheric intrusions. Regions of low aerosol scattering and enhanced O3 mixing ratios were usually correlated with descending air from the upper troposphere or lower stratosphere.

  14. Dissolved organic matter in sea spray: a transfer study from marine surface water to aerosols

    NASA Astrophysics Data System (ADS)

    Schmitt-Kopplin, P.; Liger-Belair, G.; Koch, B. P.; Flerus, R.; Kattner, G.; Harir, M.; Kanawati, B.; Lucio, M.; Tziotis, D.; Hertkorn, N.; Gebefügi, I.

    2012-04-01

    Atmospheric aerosols impose direct and indirect effects on the climate system, for example, by absorption of radiation in relation to cloud droplets size, on chemical and organic composition and cloud dynamics. The first step in the formation of Organic primary aerosols, i.e. the transfer of dissolved organic matter from the marine surface into the atmosphere, was studied. We present a molecular level description of this phenomenon using the high resolution analytical tools of Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) and nuclear magnetic resonance spectroscopy (NMR). Our experiments confirm the chemoselective transfer of natural organic molecules, especially of aliphatic compounds from the surface water into the atmosphere via bubble bursting processes. Transfer from marine surface water to the atmosphere involves a chemical gradient governed by the physicochemical properties of the involved molecules when comparing elemental compositions and differentiating CHO, CHNO, CHOS and CHNOS bearing compounds. Typical chemical fingerprints of compounds enriched in the aerosol phase were CHO and CHOS molecular series, smaller molecules of higher aliphaticity and lower oxygen content, and typical surfactants. A non-targeted metabolomics analysis demonstrated that many of these molecules corresponded to homologous series of oxo-, hydroxy-, methoxy-, branched fatty acids and mono-, di- and tricarboxylic acids as well as monoterpenes and sugars. These surface active biomolecules were preferentially transferred from surface water into the atmosphere via bubble bursting processes to form a significant fraction of primary organic aerosols. This way of sea spray production leaves a selective biological signature of the surface water in the corresponding aerosol that may be transported into higher altitudes up to the lower atmosphere, thus contributing to the formation of secondary organic aerosol on a global scale or transported laterally with

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

    NASA Astrophysics Data System (ADS)

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

    2015-12-01

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

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

    NASA Technical Reports Server (NTRS)

    Yue, G. K.; Deepak, A.

    1984-01-01

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

  17. Sea Spray Aerosol Structure and Composition Using Cryogenic Transmission Electron Microscopy

    PubMed Central

    2016-01-01

    The composition and surface properties of atmospheric aerosol particles largely control their impact on climate by affecting their ability to uptake water, react heterogeneously, and nucleate ice in clouds. However, in the vacuum of a conventional electron microscope, the native surface and internal structure often undergo physicochemical rearrangement resulting in surfaces that are quite different from their atmospheric configurations. Herein, we report the development of cryogenic transmission electron microscopy where laboratory generated sea spray aerosol particles are flash frozen in their native state with iterative and controlled thermal and/or pressure exposures and then probed by electron microscopy. This unique approach allows for the detection of not only mixed salts, but also soft materials including whole hydrated bacteria, diatoms, virus particles, marine vesicles, as well as gel networks within hydrated salt droplets—all of which will have distinct biological, chemical, and physical processes. We anticipate this method will open up a new avenue of analysis for aerosol particles, not only for ocean-derived aerosols, but for those produced from other sources where there is interest in the transfer of organic or biological species from the biosphere to the atmosphere. PMID:26878061

  18. Turbulent aerosol fluxes over the Arctic Ocean: 2. Wind-driven sources from the sea

    NASA Astrophysics Data System (ADS)

    Nilsson, E. D.; Rannik, Ü.; Swietlicki, E.; Leck, C.; Aalto, P. P.; Zhou, J.; Norman, M.

    2001-12-01

    An eddy-covariance flux system was successfully applied over open sea, leads and ice floes during the Arctic Ocean Expedition in July-August 1996. Wind-driven upward aerosol number fluxes were observed over open sea and leads in the pack ice. These particles must originate from droplets ejected into the air at the bursting of small air bubbles at the water surface. The source flux F (in 106 m-2 s-1) had a strong dependency on wind speed, log>(F>)=0.20U¯-1.71 and 0.11U¯-1.93, over the open sea and leads, respectively (where U¯ is the local wind speed at about 10 m height). Over the open sea the wind-driven aerosol source flux consisted of a film drop mode centered at ˜100 nm diameter and a jet drop mode centered at ˜1 μm diameter. Over the leads in the pack ice, a jet drop mode at ˜2 μm diameter dominated. The jet drop mode consisted of sea-salt, but oxalate indicated an organic contribution, and bacterias and other biogenic particles were identified by single particle analysis. Particles with diameters less than -100 nm appear to have contributed to the flux, but their chemical composition is unknown. Whitecaps were probably the bubble source at open sea and on the leads at high wind speed, but a different bubble source is needed in the leads owing to their small fetch. Melting of ice in the leads is probably the best candidate. The flux over the open sea was of such a magnitude that it could give a significant contribution to the condensation nuclei (CCN) population. Although the flux from the leads were roughly an order of magnitude smaller and the leads cover only a small fraction of the pack ice, the local source may till be important for the CCN population in Arctic fogs. The primary marine aerosol source will increase both with increased wind speed and with decreased ice fraction and extent. The local CCN production may therefore increase and influence cloud or fog albedo and lifetime in response to greenhouse warming in the Arctic Ocean region.

  19. Fusion of SeaWiFS and TOMS satellite data with surface observations and topographic data during extreme aerosol events.

    PubMed

    Falke, S R; Husar, R B; Schichtel, B A

    2001-11-01

    Spaceborne sensors allow near-continuous aerosol monitoring throughout the world. This paper illustrates the fusion of Sea-Viewing Wide Field-of-View Sensor (SeaWiFS) and TOMS satellite data with surface observations and topographic data during four extreme aerosol events: (1) the April 1998 Asian dust storm that impacted the west coast of North America, (2) the May 1998 Central American forest fire smoke that impacted eastern North America, (3) the intense fall 1999 northern California fires, and (4) the massive February 2000 Sahara dust storm. During these dust and smoke events, the aerosol was visualized on true color SeaWiFS images as a distinct yellowish dye, the result of the aerosol increasing the reflectance of darker surfaces (ocean and land) and decreasing the reflectance of clouds. TOMS imagery also indicated increased aerosol absorption in the affected areas, while surface monitors measured major reductions in visual range. Fusing these data aids in the determination of the aerosol's spatial, temporal, and optical properties and provides supporting evidence for characterizing what is being visualized as dust or smoke. A 3-dimensional perspective of the events is obtained when incorporating topographic data and provides insight into the vertical properties of the aerosol plumes.

  20. Accuracy Remote-Sensing of Aerosol Spatial Distribution in the Lower Troposphere by Twin Scanning Lidars

    NASA Astrophysics Data System (ADS)

    Gao, F.; Hua, D.; Li, Y.; Li, W.; Wang, L.

    2015-12-01

    Aerosols in the lower troposphere play an important role in the absorption and scattering of atmospheric radiation, the forming of precipitation and the circulation of chemistry. Due to the influence of solar heating at the surface, the aerosol distribution is inhomogeneous and variation with time. Lidar is proven to be a powerful tool in the application of remote sensing of atmospheric properties (Klett 1981). However, the existing of overlap function in lidar equation limits the fine detection of aerosol optical properties in the lower troposphere by vertical measurement, either by Raman lidar (Whiteman 2003) or by high spectral resolution lidar (Imaki 2005). Although the multi-angle method can succeed the aerosol measurement from the ground, the homogeneous atmospheric is needed (Pahlow 2004). Aiming to detect the inhomogeneous aerosols in the lower troposphere and to retrieve the aerosol extinction and backscatter coefficients in the lidar equation, a novel method for accuracy remote-sensing of aerosol properties based on twin scanning lidars has been proposed. In order to realize the fine detection of the aerosol spatial distribution from the ground to the height of interest of atmosphere, the scanning lidar is utilized as the remote sensing tool combined with the cross scanning by the twin systems, which makes the exact solutions of those two unknown parameters retrievable. Figure shows the detection method for aerosol spatial distribution using twin scanning lidars. As two lidar equations are provided simultaneously, the aerosol extinction and backscatter coefficients are retrievable. Moreover, by selecting the transmitting laser wavelength, the presented method can realize the fine detection of aerosol at any spectrum, even the theoretical and technical analysis of the aerosol characteristics by applying multi-spectra.

  1. Global distribution and climate forcing of marine organic aerosol: 1. Model improvements and evaluation

    SciTech Connect

    Meskhidze, N.; Xu, J.; Gantt, Brett; Zhang, Yang; Nenes, Athanasios; Ghan, Steven J.; Liu, Xiaohong; Easter, Richard C.; Zaveri, Rahul A.

    2011-11-23

    Marine organic aerosol emissions have been implemented and evaluated within the National Center of Atmospheric Research (NCAR)'s Community Atmosphere Model (CAM5) with the Pacific Northwest National Laboratory's 7-mode Modal Aerosol Module (MAM-7). Emissions of marine primary organic aerosols (POA), phytoplanktonproduced isoprene- and monoterpenes-derived secondary organic aerosols (SOA) and methane sulfonate (MS{sup -}) are shown to affect surface concentrations of organic aerosols in remote marine regions. Global emissions of submicron marine POA is estimated to be 7.9 and 9.4 Tg yr{sup -1}, for the Gantt et al. (2011) and Vignati et al. (2010) emission parameterizations, respectively. Marine sources of SOA and particulate MS{sup -} (containing both sulfur and carbon atoms) contribute an additional 0.2 and 5.1 Tg yr{sup -1}, respectively. Widespread areas over productive waters of the Northern Atlantic, Northern Pacific, and the Southern Ocean show marine-source submicron organic aerosol surface concentrations of 100 ngm{sup -3}, with values up to 400 ngm{sup -3} over biologically productive areas. Comparison of long-term surface observations of water insoluble organic matter (WIOM) with POA concentrations from the two emission parameterizations shows that despite revealed discrepancies (often more than a factor of 2), both Gantt et al. (2011) and Vignati et al. (2010) formulations are able to capture the magnitude of marine organic aerosol concentrations, with the Gantt et al. (2011) parameterization attaining better seasonality. Model simulations show that the mixing state of the marine POA can impact the surface number concentration of cloud condensation nuclei (CCN). The largest increases (up to 20 %) in CCN (at a supersaturation (S) of 0.2 %) number concentration are obtained over biologically productive ocean waters when marine organic aerosol is assumed to be externally mixed with sea-salt. Assuming marine organics are internally-mixed with sea

  2. IS THE SIZE DISTRIBUTION OF URBAN AEROSOLS DETERMINED BY THERMODYNAMIC EQUILIBRIUM? (R826371C005)

    EPA Science Inventory

    A size-resolved equilibrium model, SELIQUID, is presented and used to simulate the size–composition distribution of semi-volatile inorganic aerosol in an urban environment. The model uses the efflorescence branch of aerosol behavior to predict the equilibrium partitioni...

  3. Study on size distribution of total aerosol and water-soluble ions during an Asian dust storm event at Jeju Island, Korea.

    PubMed

    Park, S H; Song, C B; Kim, M C; Kwon, S B; Lee, K W

    2004-01-01

    Soil dust particles transported from loess regions of the Asian continent, called Asian dust, highly influences the air quality of north-eastern Asia and the northern Pacific Ocean. In order to investigate the effects of these dust storms on the chemical composition of atmospheric aerosol particles with different size, measurements of size distributions of total aerosol and major ion species were carried out on Jeju Island, Korea during April 2001. Juju Island was chosen for the study because the levels of emissions of anthropogenic air pollutants are very low. A 5-stage cascade impactor was used to sample size-fractionated aerosol particles. Samples were analyzed for major water-soluble ions using Dionex DX-120 ion chromatograph. The average mass concentration of total aerosol was found to be 24.4 and 108.3 microg m(-3) for non-Asian dust and Asian dust periods, respectively. The total aerosol size distribution, measured during the non-Asian dust period, was bimodal, whereas the coarse particles dominated the size distribution of total aerosol during the Asian dust period. It was found that SO4(2-), NH4+ and K+ were mainly distributed in fine particles, while Cl-, NO3-, Na+, Mg2+ and Ca2+ were in coarse particles. Although SO4(2-) was mainly distributed in fine particles, during the Asian dust period, the concentrations in coarse particles were significantly increased. This indicates heterogeneous oxidation of SO2 on wet surfaces of basic soil dust particles. The NH4+ was found to exist as (NH4)2SO4 in fine particles, with a molar ratio of NH4+ to SO4(2-) of 2.37 and 1.52 for non-Asian dust and Asian dust periods, respectively. Taking into account the proximity of the sampling site to the sea, and the observed chloride depletion, coarse mode nitrate, during the non-Asian dust period, is assumed to originate from the reaction of nitric acid with sodium chloride on the surfaces of sea-salt particles although the chloride depletion was not shown to be large enough to

  4. Global Distributions of Mineral Dust Properties from SeaWiFS and MODIS: From Sources to Sinks

    NASA Technical Reports Server (NTRS)

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

    2011-01-01

    The impact of natural and anthropogenic sources of mineral dust has gained increasing attention from scientific communities in recent years. Indeed, these airborne dust particles, once lifted over the source regions, can be transported out of the boundary layer into the free troposphere and can travel thousands of kilometers across the oceans resulting in important biogeochemical impacts on the ecosystem. Due to the relatively short lifetime (a few hours to about a week), the distributions of these mineral dust particles vary extensively in both space and time. Consequently, satellite observations are needed over both source and sink regions for continuous temporal and spatial sampling of aerosol properties. With the launch of SeaWiFS in 1997, Terra/MODIS in 1999, and Aqua/MODIS in 2002, high quality comprehensive aerosol climatology is becoming feasible for the first time. As a result of these unprecedented satellite data records, studies of the radiative and biogeochemical effects due to dust aerosols are now possible. In this study, we will show the comparisons of satellite retrieved aerosol optical thickness using Deep Blue algorithm with data from AERONET sunphotometers over desert and semi-desert regions as well as vegetated areas. Our results indicate reasonable agreements between these two. These new satellite products will allow scientists to determine quantitatively the aerosol properties near sources using high spatial resolution measurements from Sea WiFS and MODIS-like instruments. The multiyear satellite measurements since 1997 from Sea WiFS will be compared with those retrieved from MODIS and MISR, and will be utilized to investigate the interannual variability of source, pathway, and dust loading associated with the dust outbreaks over the entire globe. Finally, the trends observed over the last decade based upon the SeaWiFS time series in the amounts of tropospheric aerosols due to natural and anthropogenic sources (such as changes in the frequency

  5. 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.

  6. 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

  7. Impact of springtime biomass-burning aerosols on radiative forcing over northern Thailand during the 7SEAS campaign

    NASA Astrophysics Data System (ADS)

    Pani, Shantanu Kumar; Wang, Sheng-Hsiang; Lin, Neng-Huei; Lee, Chung-Te; Tsay, Si-Chee; Holben, Brent; Janjai, Serm; Hsiao, Ta-Chih; Chuang, Ming-Tung; Chantara, Somporn

    2016-04-01

    Biomass-burning (BB) aerosols are the significant contributor to the regional/global aerosol loading and radiation budgets. BB aerosols affect the radiation budget of the earth and atmosphere by scattering and absorbing directly the incoming solar and outgoing terrestrial radiation. These aerosols can exert either cooling or warming effect on climate, depending on the balance between scattering and absorption. BB activities in the form of wildland forest fires and agricultural crop burning are very pronounced in the Indochina peninsular regions in Southeast Asia mainly in spring (late February to April) season. The region of interest includes Doi Ang Khang (19.93° N, 99.05° E, 1536 msl) in northern Thailand, as part of the Seven South East Asian Studies (7-SEAS)/BASELInE (Biomass-burning Aerosols & Stratocumulus Environment: Lifecycles & Interactions Experiment) campaign in 2013. In this study, for the first time, the direct aerosol radiative effects of BB aerosols over near-source BB emissions, during the peak loading spring season, in northern Indochina were investigated by using ground-based physical, chemical, and optical properties of aerosols as well as the aerosol optical and radiative transfer models. Information on aerosol parameters in the field campaign was used in the OPAC (Optical Properties of Aerosols and Clouds) model to estimate various optical properties corresponding to aerosol compositions. Clear-sky shortwave direct aerosol radiative effects were further estimated with a raditive transfer model SBDART (Santa Barbara DISORT Atmospheric Radiative Transfer). The columnar aerosol optical depth (AOD500) was found to be ranged from 0.26 to 1.13 (with the mean value 0.71 ± 0.24). Fine-mode (fine mode fraction ≈0.98, angstrom exponent ≈1.8) and significantly absorbing aerosols (columnar single-scattering albedo ≈0.89, asymmetry-parameter ≈0.67 at 441 nm wavelength) dominated in this region. Water soluble and black carbon (BC) aerosols mainly

  8. Aerosol Optical Depth Distribution in Extratropical Cyclones over the Northern Hemisphere Oceans

    NASA Technical Reports Server (NTRS)

    Naud, Catherine M.; Posselt, Derek J.; van den Heever, Susan C.

    2016-01-01

    Using Moderate Resolution Imaging Spectroradiometer and an extratropical cyclone database,the climatological distribution of aerosol optical depth (AOD) in extratropical cyclones is explored based solely on observations. Cyclone-centered composites of aerosol optical depth are constructed for the Northern Hemisphere mid-latitude ocean regions, and their seasonal variations are examined. These composites are found to be qualitatively stable when the impact of clouds and surface insolation or brightness is tested. The larger AODs occur in spring and summer and are preferentially found in the warm frontal and in the post-cold frontal regions in all seasons. The fine mode aerosols dominate the cold sector AODs, but the coarse mode aerosols display large AODs in the warm sector. These differences between the aerosol modes are related to the varying source regions of the aerosols and could potentially have different impacts on cloud and precipitation within the cyclones.

  9. Impact of aerosol vertical distribution on aerosol direct radiative effect and heating rate in the Mediterranean region

    NASA Astrophysics Data System (ADS)

    Pappas, Vasileios; Hatzianastassiou, Nikolaos; Matsoukas, Christos; Koras Carracca, Mario; Kinne, Stefan; Vardavas, Ilias

    2015-04-01

    It is now well-established that aerosols cause an overall cooling effect at the surface and a warming effect within the atmosphere. At the top of the atmosphere (TOA), both positive and negative forcing can be found, depending on a number of other factors, such as surface albedo and relative position of clouds and aerosols. Whilst aerosol surface cooling is important due to its relation with surface temperature and other bio-environmental reasons, atmospheric heating is of special interest as well having significant impacts on atmospheric dynamics, such as formation of clouds and subsequent precipitation. The actual position of aerosols and their altitude relative to clouds is of major importance as certain types of aerosol, such as black carbon (BC) above clouds can have a significant impact on planetary albedo. The vertical distribution of aerosols and clouds has recently drawn the attention of the aerosol community, because partially can account for the differences between simulated aerosol radiative forcing with various models, and therefore decrease the level of our uncertainty regarding aerosol forcing, which is one of our priorities set by IPCC. The vertical profiles of aerosol optical and physical properties have been studied by various research groups around the world, following different methodologies and using various indices in order to present the impact of aerosols on radiation on different altitudes above the surface. However, there is still variability between the published results as to the actual effect of aerosols on shortwave radiation and on heating rate within the atmosphere. This study uses vertical information on aerosols from the Max Planck Aerosol Climatology (MAC-v1) global dataset, which is a combination of model output with quality ground-based measurements, in order to provide useful insight into the vertical profile of atmospheric heating for the Mediterranean region. MAC-v1 and the science behind this aerosol dataset have already

  10. Distribution characteristics of marine litter on the sea bed of the East China Sea and the South Sea of Korea

    NASA Astrophysics Data System (ADS)

    Lee, Dae-In; Cho, Hyeon-Seo; Jeong, Sun-Beom

    2006-10-01

    The types, quantities, and distribution of marine litter found on the sea bed of the East China Sea and the South Sea of Korea are surveyed. Surveys were evaluated using bottom trawl nets during 1996-2005 cruises. Mean distribution densities were high in coastal seas, especially in the South Sea of Korea offshore from Yeosu, with 109.8 kg km -2, and low in the East China Sea, with densities of 30.6 kg km -2. Fishing gear, such as pots, nets, octopus jars, and fishing lines, accounted for about 42-72% and 37-62% of litter items in the East China Sea and the South Sea of Korea, respectively, whereas the contributions of rubber, vinyl, metal, plastic, glass, wood, and clothing were below 30% mainly. Rope and drum composition fluctuated greatly, between 54% and 0%. Eel and net pots dominated the marine debris of the South Sea of Korea, and some vinyl, plastics, and fishing gear made in Korea, China, and Japan were collected in abundance in the East China Sea. Fishing gear was probably discarded into the sea, deliberately or inadvertently, by fishing operations. A comprehensive joint approach by Korea, China, and Japan is needed for the continuous monitoring of input sources, the actual conditions, and the behavior of marine litter for protection against litter pollution and fisheries resource management in this area.

  11. An Overview of Regional Experiments on Biomass Burning Aerosols and Related Pollutants in Southeast Asia: From BASE-ASIA and the Dongsha Experiment to 7-SEAS

    NASA Technical Reports Server (NTRS)

    Lin, Neng-Huei; Tsay, Si-Chee; Maring, Hal B.; Yen, Ming-Cheng; Sheu, Guey-Rong; Wang, Sheng-Hsiang; Chi, Kai Hsien; Chuang, Ming-Tung; Ou-Yang, Chang-Feng; Fu, Joshua S.; Reid, Jeffrey S.; Lee, Chung-Te; Wang, Lin-Chi; Wang, Jia-Lin; Hsu, Christina N.; Sayer, Andrew M.; Holben, Brent N.; Chu, Yu-Chi; Nguyen, Xuan Anh; Sopajaree, Khajornsak; Chen, Shui-Jen; Cheng, Man-Ting; Tsuang, Ben-Jei; Tsai, Chuen-Jinn; Peng, Chi-Ming; Schnell, Russell C.; Conway, Tom; Chang, Chang-Tang; Lin, Kuen-Song; Tsai, Ying I.; Lee, Wen-Jhy; Chang, Shuenn-Chin; Liu, Jyh-Jian; Chang, Wei-Li; Huang, Shih-Jen; Lin, Tang-Huang; Liu, Gin-Rong

    2013-01-01

    By modulating the Earth-atmosphere energy, hydrological and biogeochemical cycles, and affecting regional-to-global weather and climate, biomass burning is recognized as one of the major factors affecting the global carbon cycle. However, few comprehensive and wide-ranging experiments have been conducted to characterize biomass-burning pollutants in Southeast Asia (SEA) or assess their regional impact on meteorology, the hydrological cycle, the radiative budget, or climate change. Recently, BASEASIA (Biomass-burning Aerosols in South-East Asia: Smoke Impact Assessment) and the 7-SEAS (7- South-East Asian Studies) Dongsha Experiment were conducted during the spring seasons of 2006 and 2010 in northern SEA, respectively, to characterize the chemical, physical, and radiative properties of biomass-burning emissions near the source regions, and assess their effects. This paper provides an overview of results from these two campaigns and related studies collected in this special issue, entitled Observation, modeling and impact studies of biomass burning and pollution in the SE Asian Environment. This volume includes 28 papers, which provide a synopsis of the experiments, regional weatherclimate, chemical characterization of biomass-burning aerosols and related pollutants in source and sink regions, the spatial distribution of air toxics (atmospheric mercury and dioxins) in source and remote areas, a characterization of aerosol physical, optical, and radiative properties, as well as modeling and impact studies. These studies, taken together, provide the first relatively complete dataset of aerosol chemistry and physical observations conducted in the sourcesink region in the northern SEA, with particular emphasis on the marine boundary layer and lower free troposphere (LFT). The data, analysis and modeling included in these papers advance our present knowledge of source characterization of biomass-burning pollutants near the source regions as well as the physical and

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

    PubMed

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

    2015-08-01

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

  13. Spatial variation of biogenic sulfur in the south Yellow Sea and the East China Sea during summer and its contribution to atmospheric sulfate aerosol.

    PubMed

    Zhang, Sheng-Hui; Yang, Gui-Peng; Zhang, Hong-Hai; Yang, Jian

    2014-08-01

    Spatial distributions of biogenic sulfur compounds including dimethylsulfide (DMS), dissolved and particulate dimethylsulfoniopropionate (DMSPd and DMSPp) were investigated in the South Yellow Sea (SYS) and the East China Sea (ECS) in July 2011. The concentrations of DMS and DMSPp were significantly correlated with the levels of chlorophyll a in the surface water. Simultaneously, relatively high ratio values of DMSP/chlorophyll a and DMS/chlorophyll a occurred in the areas where the phytoplankton community was dominated by dinoflagellates. The DMSPp and chlorophyll a size-fractionation showed that larger nanoplankton (5-20 μm) was the most important producer of DMSPp in the study area. The vertical profiles of DMS and DMSP were characterized by a maximum at the upper layer and the bottom concentrations were also relatively higher compared with the overlying layer of the bottom. In addition, a positive linear correlation was observed between dissolved dimethylsulfoxide (DMSOd) and DMS concentrations in the surface waters. The sea-to-air fluxes of DMS in the study area were estimated to be from 0.03 to 102.35 μmol m(-2) d(-1) with a mean of 16.73 μmol m(-2) d(-1) and the contribution of biogenic non-sea-salt SO4(2-) (nss-SO4(2-)) to the measured total nss-SO4(2-) in the atmospheric aerosol over the study area varied from 1.42% to 30.98%, with an average of 8.2%.

  14. A new stochastic algorithm for inversion of dust aerosol size distribution

    NASA Astrophysics Data System (ADS)

    Wang, Li; Li, Feng; Yang, Ma-ying

    2015-08-01

    Dust aerosol size distribution is an important source of information about atmospheric aerosols, and it can be determined from multiwavelength extinction measurements. This paper describes a stochastic inverse technique based on artificial bee colony (ABC) algorithm to invert the dust aerosol size distribution by light extinction method. The direct problems for the size distribution of water drop and dust particle, which are the main elements of atmospheric aerosols, are solved by the Mie theory and the Lambert-Beer Law in multispectral region. And then, the parameters of three widely used functions, i.e. the log normal distribution (L-N), the Junge distribution (J-J), and the normal distribution (N-N), which can provide the most useful representation of aerosol size distributions, are inversed by the ABC algorithm in the dependent model. Numerical results show that the ABC algorithm can be successfully applied to recover the aerosol size distribution with high feasibility and reliability even in the presence of random noise.

  15. Longitudinal variability of the biogeochemical role of Mediterranean aerosols in the Mediterranean Sea

    NASA Astrophysics Data System (ADS)

    Ternon, E.; Guieu, C.; Ridame, C.; L'Helguen, S.; Catala, P.

    2010-11-01

    The Mediterranean Sea is a semi-enclosed basin characterized by a strong thermal stratification during summer during which the atmosphere is the main source of new nutrients to the nutrient-depleted surface layer. From aerosol sampling and microcosm experiments performed during the TransMed BOUM cruise (June-July 2008) we showed that: (i) the Mediterranean atmosphere composition (Al, Fe, P) was homogeneous over ~28° of longitude and was a mixture with a constant proportion of anthropogenic contribution and a variable but modest contribution of crustal aerosols. This quite stable composition over a one month period and a long transect (~2500 km) allowed to define the Mediterranean atmospheric "background" that characterizes the summer season in the absence of major Saharan event and forest fires, (ii) primary production significantly increased at all tested stations after aerosols addition collected on-board and after Saharan dust analog addition, indicating that both additions relieved on-going (co)-limitations. Although both additions significantly increased the N2 fixation rates at the western station, diazotrophic activity remained very low (~0.2 nmol N L-1 d-1), (iii) due to the presence of anthropogenic particles, the probable higher solubility of nutrients associated with mixed aerosols (crustal + anthropogenic contribution), conferred a higher fertilizing potential to on-board collected aerosol as compared to Saharan dust analog. Finally, those experiments showed that atmospheric inputs from a mixed atmospheric event ("summer rain" type) or from a high-intensity Saharan event would induce comparable response by the biota in the stratified Mediterranean SML, during summer.

  16. Longitudinal variability of the biogeochemical role of Mediterranean aerosols in the Mediterranean Sea

    NASA Astrophysics Data System (ADS)

    Ternon, E.; Guieu, C.; Ridame, C.; L'Helguen, S.; Catala, P.

    2011-05-01

    The Mediterranean Sea is a semi-enclosed basin characterized by a strong thermal stratification during summer during which the atmosphere is the main source of new nutrients to the nutrient-depleted surface layer. From aerosol sampling and microcosm experiments performed during the TransMed BOUM cruise (June-July 2008) we showed that: (i) the Mediterranean atmosphere composition (Al, Fe, P) was homogeneous over ~28° of longitude and was a mixture with a constant proportion of anthropogenic contribution and a variable but modest contribution of crustal aerosols. This quite stable composition over a one month period and a long transect (~2500 km) allowed to define the Mediterranean atmospheric "background" that characterizes the summer season in the absence of major Saharan event and forest fires, (ii) primary production significantly increased at all tested stations after aerosols addition collected on-board and after Saharan dust analog addition, indicating that both additions relieved on-going (co)-limitations. Although both additions significantly increased the N2 fixation rates at the western station, diazotrophic activity remained very low (~0.2 nmol N L-1 d-1), (iii) due to the presence of anthropogenic particles, the probable higher solubility of nutrients associated with mixed aerosols (crustal + anthropogenic contribution), conferred a higher fertilizing potential to on-board collected aerosol as compared to Saharan dust analog. Finally, those experiments showed that atmospheric inputs from a mixed atmospheric event ("summer rain" type) or from a high-intensity Saharan event would induce comparable response by the biota in the stratified Mediterranean SML, during summer.

  17. Balloon-borne measurement of the aerosol size distribution from an Icelandic flood basalt eruption

    NASA Astrophysics Data System (ADS)

    Vignelles, D.; Roberts, T. J.; Carboni, E.; Ilyinskaya, E.; Pfeffer, M.; Dagsson Waldhauserova, P.; Schmidt, A.; Berthet, G.; Jegou, F.; Renard, J.-B.; Ólafsson, H.; Bergsson, B.; Yeo, R.; Fannar Reynisson, N.; Grainger, R. G.; Galle, B.; Conde, V.; Arellano, S.; Lurton, T.; Coute, B.; Duverger, Vincent

    2016-11-01

    We present in situ balloon-borne measurements of aerosols in a volcanic plume made during the Holuhraun eruption (Iceland) in January 2015. The balloon flight intercepted a young plume at 8 km distance downwind from the crater, where the plume is ∼15 min of age. The balloon carried a novel miniature optical particle counter LOAC (Light Optical Aerosol Counter) which measures particle number concentration and size distribution in the plume, alongside a meteorological payload. We discuss the possibility of calculating particle flux by combining LOAC data with measurements of sulfur dioxide flux by ground-based UV spectrometer (DOAS). The balloon passed through the plume at altitude range of 2.0-3.1 km above sea level (a.s.l.). The plume top height was determined as 2.7-3.1 km a.s.l., which is in good agreement with data from Infrared Atmospheric Sounding Interferometer (IASI) satellite. Two distinct plume layers were detected, a non-condensed lower layer (300 m thickness) and a condensed upper layer (800 m thickness). The lower layer was characterized by a lognormal size distribution of fine particles (0.2 μm diameter) and a secondary, coarser mode (2.3 μm diameter), with a total particle number concentration of around 100 cm-3 in the 0.2-100 μm detection range. The upper layer was dominated by particle centered on 20 μm in diameter as well as containing a finer mode (2 μm diameter). The total particle number concentration in the upper plume layer was an order of magnitude higher than in the lower layer. We demonstrate that intercepting a volcanic plume with a meteorological balloon carrying LOAC is an efficient method to characterize volcanic aerosol properties. During future volcanic eruptions, balloon-borne measurements could be carried out easily and rapidly over a large spatial area in order to better characterize the evolution of the particle size distribution and particle number concentrations in a volcanic plume.

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

    NASA Astrophysics Data System (ADS)

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

    2016-04-01

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

  19. Sea salt aerosol deposition in the coastal zone: A large eddy simulation study

    NASA Astrophysics Data System (ADS)

    Liang, Tinghao; Chamecki, Marcelo; Yu, Xiping

    2016-11-01

    Inland deposition of sea salt aerosol (SSA) particles emitted over the ocean is studied via numerical and theoretical models. The focus is on the large particles that contribute most to the total mass deposition. Large eddy simulations of idealized sea wind are used to investigate the development of the particle plume over land for different particle sizes and to validate some of the assumptions in the theoretical model. An existing theoretical modeling framework for particle dispersion in the atmospheric boundary layer is adapted to the problem of SSA deposition and it is shown to be adequate for the large particles of interest here. The decay of monodisperse SSA particle deposition flux with distance from the shoreline is shown to have a power-law behavior far from the shoreline. A complete model for predicting mass deposition as a function of distance is formulated and shown to present reasonable agreement with existing data.

  20. Size distribution of chromate paint aerosol generated in a bench-scale spray booth.

    PubMed

    Sabty-Daily, Rania A; Hinds, William C; Froines, John R

    2005-01-01

    Spray painters are potentially exposed to aerosols containing hexavalent chromium [Cr(VI)] via inhalation of chromate-based paint sprays. Evaluating the particle size distribution of a paint spray aerosol, and the variables that may affect this distribution, is necessary to determine the site and degree of respiratory deposition and the damage that may result from inhaled Cr(VI)-containing paint particles. This study examined the effect of spray gun atomization pressure, aerosol generation source and aerosol aging on the size distribution of chromate-based paint overspray aerosols generated in a bench-scale paint spray booth. The study also determined the effect of particle bounce inside a Marple personal cascade impactor on measured size distributions of paint spray aerosols. Marple personal cascade impactors with a modified inlet were used for sample collection. The data indicated that paint particle bounce did not occur inside the cascade impactors sufficiently to affect size distribution when using uncoated stainless steel or PVC substrate sampling media. A decrease in paint aerosol mass median aerodynamic diameter (MMAD) from 8.2 to 7.0 mum was observed as gun atomization pressure increased from 6 to 10 psi. Overspray aerosols were sampled at two locations in the spray booth. A downstream sampling position simulated the exposure of a worker standing between the painted surface and exhaust, a situation encountered in booths with multiple workers. The measured mean MMAD was 7.2 mum. The distance between the painted surface and sampler was varied to sample oversprays of varying ages between 2.8 and 7.7 s. Age was not a significant factor for determining MMAD. Overspray was sampled at a 90 degrees position to simulate a worker standing in front of the surface being painted with air flowing to the worker's side, a common situation in field applications. The resulting overspray MMAD averaged 5.9 mum. Direct-spray aerosols were sampled at ages from 5.3 to 11.7 s

  1. Study on distribution of aerosol optical depth in Chongqing urban area

    NASA Astrophysics Data System (ADS)

    Yang, Shiqi; Liu, Can; Gao, Yanghua

    2015-12-01

    This paper selected 6S (second simulation of the satellite signal in the solar spectrum) model with dark pixel method to inversion aerosol optical depth by MODIS data, and got the spatial distribution and the temporal distribution of Chongqing urban area. By comparing with the sun photometer and API data, the result showed that the inversion method can be used in aerosol optical thickness monitoring in Chongqing urban area.

  2. [Seasonal variations in the vertical distribution of aerosols during dry haze periods in regions around Shanghai].

    PubMed

    Xu, Ting-Ting; Qing, Yan; Geng, Fu-Hai; Chen, Yong-Hang; Zhang, Hua; Liu, Qiong; Ma, Xiao-Jun

    2012-07-01

    Based on the onboard lidar data from CALIPSO satellite of National Aeronautics and Space Administration (NASA) from January 2007 to November 2010, the vertical distribution of optical and micro-physical properties of aerosols around Shanghai during the haze periods when relative humidity less than 80% were revealed by analyzing the parameters of 532 nm total attenuated backscatter coefficient, volume depolarization ratio and total attenuated color ratio. The results showed that during dry haze periods, the scattering ability of lower troposphere (0-2 km) was the highest and the main constituents were regular aerosols. The scattering ability of the upper troposphere (8-10 km) was the lowest and the proportion of irregular aerosols was the highest among the five altitude layers. In addition, the scattering ability of the altitude range (2-8 km) was lower than that of the lower troposphere, and the scattering ability and irregularity of aerosols at different altitude levels within the range were close to each other. Fine particle aerosols were the dominant aerosols in altitude range of 0-10 km. To be noted, the proportion of fine particles decreased with increasing altitude within the altitude range of 2-8 km. The proportion of large and irregular aerosols were higher in spring, whereas the proportion of fine and regular aerosols were higher in summer. According to the analysis of a dry haze episode on May 7th, 2007, it was found that a mass of aerosols mainly distributed within the altitude range of 0-1.5 km and partially within the altitude range of 4.0-5.5 km. The HYSPLIT model was applied to analyze the sources of aerosols in the episode, and the results indicated that the dry haze was mainly caused not only by local emissions but also by the dust aerosols transported from Mongolia, the northwest and north of China by the airflow.

  3. Aerosol and gas re-distribution by shallow cumulus clouds: An investigation using airborne measurements

    NASA Astrophysics Data System (ADS)

    Wonaschuetz, Anna; Sorooshian, Armin; Ervens, Barbara; Chuang, Patrick Y.; Feingold, Graham; Murphy, Shane M.; de Gouw, Joost; Warneke, Carsten; Jonsson, Haflidi H.

    2012-09-01

    Aircraft measurements during the 2006 Gulf of Mexico Atmospheric Composition and Climate Study (GoMACCS) are used to examine the influence of shallow cumulus clouds on vertical profiles of aerosol chemical composition, size distributions, and secondary aerosol precursor gases. The data show signatures of convective transport of particles, gases and moisture from near the surface to higher altitudes, and of aqueous-phase production of aerosol mass (sulfate and organics) in cloud droplets and aerosol water. In cloudy conditions, the average aerosol volume concentration at an altitude of 2850 m, above typical cloud top levels, was found to be 34% of that at 450 m; for clear conditions, the same ratio was 13%. Both organic and sulfate mass fractions were on average constant with altitude (around 50%); however, the ratio of oxalate to organic mass increased with altitude (from 1% at 450 m to almost 9% at 3450 m), indicative of the influence of in-cloud production on the vertical abundance and characteristics of secondary organic aerosol (SOA) mass. A new metric termed "residual cloud fraction" is introduced as a way of quantifying the "cloud processing history" of an air parcel. Results of a parcel model simulating aqueous phase production of sulfate and organics reproduce observed trends and point at a potentially important role of SOA production, especially oligomers, in deliquesced aerosols. The observations emphasize the importance of shallow cumulus clouds in altering the vertical distribution of aerosol properties that influence both their direct and indirect effect on climate.

  4. Parametric retrieval model for estimating aerosol size distribution via the AERONET, LAGOS station.

    PubMed

    Emetere, Moses Eterigho; Akinyemi, Marvel Lola; Akin-Ojo, Omololu

    2015-12-01

    The size characteristics of atmospheric aerosol over the tropical region of Lagos, Southern Nigeria were investigated using two years of continuous spectral aerosol optical depth measurements via the AERONET station for four major bands i.e. blue, green, red and infrared. Lagos lies within the latitude of 6.465°N and longitude of 3.406°E. Few systems of dispersion model was derived upon specified conditions to solve challenges on aerosols size distribution within the Stokes regime. The dispersion model was adopted to derive an aerosol size distribution (ASD) model which is in perfect agreement with existing model. The parametric nature of the formulated ASD model shows the independence of each band to determine the ASD over an area. The turbulence flow of particulates over the area was analyzed using the unified number (Un). A comparative study via the aid of the Davis automatic weather station was carried out on the Reynolds number, Knudsen number and the Unified number. The Reynolds and Unified number were more accurate to describe the atmospheric fields of the location. The aerosols loading trend in January to March (JFM) and August to October (ASO) shows a yearly 15% retention of aerosols in the atmosphere. The effect of the yearly aerosol retention can be seen to partly influence the aerosol loadings between October and February. PMID:26452005

  5. Size distribution, composition and origin of the submicron aerosol in the marine boundary layer during the eastern Mediterranean "SUB-AERO" experiment

    NASA Astrophysics Data System (ADS)

    Eleftheriadis, K.; Colbeck, I.; Housiadas, C.; Lazaridis, M.; Mihalopoulos, N.; Mitsakou, C.; Smolík, J.; Ždímal, V.

    A period of intensive physical and chemical aerosol characterisation measurements was held over 5 days during July 2000 as part of the European SUB-AERO experiment.. Concurrent measurements were performed at the Finokalia remote coastal site on the island of Crete (Greece) and onboard the R/V " Aegaeon" which cruised in south part of the Aegean Sea northwards of Crete. The objective of the study was to investigate the spatial and temporal variability of microphysical parameters of the submicron aerosol and their dependence on airmass origin and chemical composition. The results reflect the submicron aerosol properties during airmass transport from the north including Europe and the Balkans and are in line with other studies on the aerosol properties of polluted continental air entering the marine boundary layer (MBL). Concentrations of submicron particulate matter (PM) mass were relatively higher at sea (20 μg m -3) compared to the coastal site (16 μg m -3). Concentrations of both organic carbon and sulphate, being the major water soluble component, were also higher at sea than at land. The high concentrations of ammonium and those of the water soluble organics, such as oxalate, can be attributed to emissions from mainland forest fires. The submicron aerosol number size distribution was unimodal with mobility mean diameters ( dg) ranging from 98 to 144 μm and standard deviations ( σg) from 1.56 to 1.9. Aerosol number concentrations at Finokalia were at least 50% lower especially when R/V Aegaeon sampled polluted air, but the modal parameters of the size distribution were very similar ( dg: 111-120, σg: 1.55-1.91). The surface MBL, under these conditions, was an aerosol rich environment where aerosol particles were transported both by the surface wind, advected from higher layers, chemically processed by interactions with gaseous precursors and physically altered by water vapour. The number to volume ratio for the submicrometer aerosol fraction reflected the

  6. Bringing the ocean into the laboratory to probe the chemical complexity of sea spray aerosol

    PubMed Central

    Prather, Kimberly A.; Bertram, Timothy H.; Grassian, Vicki H.; Deane, Grant B.; Stokes, M. Dale; DeMott, Paul J.; Aluwihare, Lihini I.; Palenik, Brian P.; Azam, Farooq; Seinfeld, John H.; Moffet, Ryan C.; Molina, Mario J.; Cappa, Christopher D.; Geiger, Franz M.; Roberts, Gregory C.; Russell, Lynn M.; Ault, Andrew P.; Baltrusaitis, Jonas; Collins, Douglas B.; Corrigan, Craig E.; Cuadra-Rodriguez, Luis A.; Ebben, Carlena J.; Forestieri, Sara D.; Guasco, Timothy L.; Hersey, Scott P.; Kim, Michelle J.; Lambert, William F.; Modini, Robin L.; Mui, Wilton; Pedler, Byron E.; Ruppel, Matthew J.; Ryder, Olivia S.; Schoepp, Nathan G.; Sullivan, Ryan C.; Zhao, Defeng

    2013-01-01

    The production, size, and chemical composition of sea spray aerosol (SSA) particles strongly depend on seawater chemistry, which is controlled by physical, chemical, and biological processes. Despite decades of studies in marine environments, a direct relationship has yet to be established between ocean biology and the physicochemical properties of SSA. The ability to establish such relationships is hindered by the fact that SSA measurements are typically dominated by overwhelming background aerosol concentrations even in remote marine environments. Herein, we describe a newly developed approach for reproducing the chemical complexity of SSA in a laboratory setting, comprising a unique ocean-atmosphere facility equipped with actual breaking waves. A mesocosm experiment was performed in natural seawater, using controlled phytoplankton and heterotrophic bacteria concentrations, which showed SSA size and chemical mixing state are acutely sensitive to the aerosol production mechanism, as well as to the type of biological species present. The largest reduction in the hygroscopicity of SSA occurred as heterotrophic bacteria concentrations increased, whereas phytoplankton and chlorophyll-a concentrations decreased, directly corresponding to a change in mixing state in the smallest (60–180 nm) size range. Using this newly developed approach to generate realistic SSA, systematic studies can now be performed to advance our fundamental understanding of the impact of ocean biology on SSA chemical mixing state, heterogeneous reactivity, and the resulting climate-relevant properties. PMID:23620519

  7. Bringing the ocean into the laboratory to probe the chemical complexity of sea spray aerosol.

    PubMed

    Prather, Kimberly A; Bertram, Timothy H; Grassian, Vicki H; Deane, Grant B; Stokes, M Dale; Demott, Paul J; Aluwihare, Lihini I; Palenik, Brian P; Azam, Farooq; Seinfeld, John H; Moffet, Ryan C; Molina, Mario J; Cappa, Christopher D; Geiger, Franz M; Roberts, Gregory C; Russell, Lynn M; Ault, Andrew P; Baltrusaitis, Jonas; Collins, Douglas B; Corrigan, Craig E; Cuadra-Rodriguez, Luis A; Ebben, Carlena J; Forestieri, Sara D; Guasco, Timothy L; Hersey, Scott P; Kim, Michelle J; Lambert, William F; Modini, Robin L; Mui, Wilton; Pedler, Byron E; Ruppel, Matthew J; Ryder, Olivia S; Schoepp, Nathan G; Sullivan, Ryan C; Zhao, Defeng

    2013-05-01

    The production, size, and chemical composition of sea spray aerosol (SSA) particles strongly depend on seawater chemistry, which is controlled by physical, chemical, and biological processes. Despite decades of studies in marine environments, a direct relationship has yet to be established between ocean biology and the physicochemical properties of SSA. The ability to establish such relationships is hindered by the fact that SSA measurements are typically dominated by overwhelming background aerosol concentrations even in remote marine environments. Herein, we describe a newly developed approach for reproducing the chemical complexity of SSA in a laboratory setting, comprising a unique ocean-atmosphere facility equipped with actual breaking waves. A mesocosm experiment was performed in natural seawater, using controlled phytoplankton and heterotrophic bacteria concentrations, which showed SSA size and chemical mixing state are acutely sensitive to the aerosol production mechanism, as well as to the type of biological species present. The largest reduction in the hygroscopicity of SSA occurred as heterotrophic bacteria concentrations increased, whereas phytoplankton and chlorophyll-a concentrations decreased, directly corresponding to a change in mixing state in the smallest (60-180 nm) size range. Using this newly developed approach to generate realistic SSA, systematic studies can now be performed to advance our fundamental understanding of the impact of ocean biology on SSA chemical mixing state, heterogeneous reactivity, and the resulting climate-relevant properties.

  8. Bringing the ocean into the laboratory to probe the chemical complexity of sea spray aerosol.

    PubMed

    Prather, Kimberly A; Bertram, Timothy H; Grassian, Vicki H; Deane, Grant B; Stokes, M Dale; Demott, Paul J; Aluwihare, Lihini I; Palenik, Brian P; Azam, Farooq; Seinfeld, John H; Moffet, Ryan C; Molina, Mario J; Cappa, Christopher D; Geiger, Franz M; Roberts, Gregory C; Russell, Lynn M; Ault, Andrew P; Baltrusaitis, Jonas; Collins, Douglas B; Corrigan, Craig E; Cuadra-Rodriguez, Luis A; Ebben, Carlena J; Forestieri, Sara D; Guasco, Timothy L; Hersey, Scott P; Kim, Michelle J; Lambert, William F; Modini, Robin L; Mui, Wilton; Pedler, Byron E; Ruppel, Matthew J; Ryder, Olivia S; Schoepp, Nathan G; Sullivan, Ryan C; Zhao, Defeng

    2013-05-01

    The production, size, and chemical composition of sea spray aerosol (SSA) particles strongly depend on seawater chemistry, which is controlled by physical, chemical, and biological processes. Despite decades of studies in marine environments, a direct relationship has yet to be established between ocean biology and the physicochemical properties of SSA. The ability to establish such relationships is hindered by the fact that SSA measurements are typically dominated by overwhelming background aerosol concentrations even in remote marine environments. Herein, we describe a newly developed approach for reproducing the chemical complexity of SSA in a laboratory setting, comprising a unique ocean-atmosphere facility equipped with actual breaking waves. A mesocosm experiment was performed in natural seawater, using controlled phytoplankton and heterotrophic bacteria concentrations, which showed SSA size and chemical mixing state are acutely sensitive to the aerosol production mechanism, as well as to the type of biological species present. The largest reduction in the hygroscopicity of SSA occurred as heterotrophic bacteria concentrations increased, whereas phytoplankton and chlorophyll-a concentrations decreased, directly corresponding to a change in mixing state in the smallest (60-180 nm) size range. Using this newly developed approach to generate realistic SSA, systematic studies can now be performed to advance our fundamental understanding of the impact of ocean biology on SSA chemical mixing state, heterogeneous reactivity, and the resulting climate-relevant properties. PMID:23620519

  9. The effect of aerosols and sea surface temperature on China's climate over the late twentieth century

    NASA Astrophysics Data System (ADS)

    Folini, Doris; Wild, Martin

    2015-04-01

    Focusing on China in the second half of the twentieth century, we examine the relative role of aerosols and prescribed, observation based sea surface temperatures (SSTs) for the evolution of surface solar radiation (SSR), surface air temperature (SAT), and precipitation in ensembles of transient (1870 - 2005) sensitivity experiments with the global climate model ECHAM5-HAM. Observations and simulations with transient SSTs and aerosol emissions agree reasonably well in eastern China in terms of SSR dimming (-6 +/- 2 W/m2/decade, 1960 - 2000), statistically non-significant JJA SAT trend (1950 - 2000), and drying in JJA from 1950 to 1990 (-2.5% to -3.5% per decade, essentially via reduction of convective precipitation). Other major observed features are not reproduce by the model, e.g. precipitation increase in the 1990s in the Yangtze valley, the strong warming in winter in northern parts of China and Mongolia, or SSR dimming in western China. For the model results, SO2 emissions are more relevant than emissions of black and organic carbon. Aerosol effects are less pronounced at higher model resolution. Transient SSTs are found to be crucial for decadal scale SAT variability over land, especially the strong warming in the 1990s, and, via SST forced reduction of cloud cover, for the ceasing of SSR dimming around the year 2000. Unforced cloud variability leads to relevant scatter (up to +/- 2 W/m2/decade) of modeled SSR trends at individual observation sites.

  10. Effect of phytoplankton biomass in seawater on chemical properties of sea spray aerosols.

    PubMed

    Park, Jiyeon; Kim, Dohyung; Lee, Kwangyul; Han, Seunghee; Kim, Hyunji; Williams, Leah R; Joo, Hung Soo; Park, Kihong

    2016-09-15

    This study is to investigate the effect of biological seawater properties on sea spray aerosols (SSA). Concentrations of chlorophyll-a and bacteria were measured at coastal site in Korea in fall and summer seasons. Also, aerosol mass spectrometer (AMS) was used to determine chemical constituents (organics, sulfate, nitrate, ammonium, and chloride) of non-refractory submicrometer aerosols sprayed from seawaters using a bubble bursting system. The average concentration of chlorophyll-a in seawater in fall was 1.75±0.78μg/l, whereas it significantly increased to 5.11±2.16μg/l in summer. It was found that the fraction of organics in the submicrometer SSA was higher in summer (68%) than fall (49%), and that the organic fraction in the SSA increased as the concentration of chlorophyll-a increased in seawater, suggesting that the high phytoplankton biomass in seawater could lead to the enhancement of organic species in the SSA.

  11. The Impact of Different Regimes in Estimating the Effects of Aerosols on Clouds. A Case Study over the Baltic Sea Countries.

    NASA Astrophysics Data System (ADS)

    Saponaro, G.

    2015-12-01

    The present study investigates the use of long-term satellite data to assess the influence of aerosols upon cloud parameters over the Baltic Sea region. This particular area offers the contrast of a very clean environment (Fennoscandia) against a more polluted one (Germany, Poland). The datasets used in this study consist of Collection 6 Level 3 daily observations from 2002 to 2014 retrieved from observations by the NASA's Moderate-Resolution Imaging Spectrometer (MODIS) instrument on-board the Aqua platform. The MODIS aerosol optical depth (AOD) and aerosol index (AI) products are used as a proxy for the number concentration of aerosol particles while the cloud effective radius (CER) and cloud optical thickness (COT) describe cloud microphysical and optical properties respectively. Through the analysis of a 12-years dataset, distribution maps provide information on a regional scale about the first aerosol indirect effect (AIE) by determining the aerosol-cloud interaction (ACI). The ACI is defined as the change in cloud optical depth or effective radius as a function of aerosol load, for which AI is used as a proxy, for a fixed liquid water path (LWP). Reanalysis data from ECMWF, namely ERA-Interim, are used to estimate meteorological settings on a regional scale. The relative humidity (RH) and specific humidity (SH) are chosen at the pressure level of 950 hPa and they are linearly interpolated to match MODIS resolution of 1 x 1 deg. The Lower Tropospheric Stability (LTS) is computed from the ERA- Interim reanalysis data as the difference between the potential temperature at 700hPa and the surface. In order to better identify and interpret the AIE, this study proposes a framework where the interactions between aerosols and clouds are estimated by dividing the dataset into different regimes. Regimes are defined by: Liquid Water Path (LWP). The discrimination by LWP allows assessing the Twomey effect. The AIE is more evident when the LWP is lower. Aerosol loading

  12. On the evaluation of global sea-salt aerosol models at coastal/orographic sites

    NASA Astrophysics Data System (ADS)

    Spada, M.; Jorba, O.; Pérez García-Pando, C.; Janjic, Z.; Baldasano, J. M.

    2015-01-01

    Sea-salt aerosol global models are typically evaluated against concentration observations at coastal stations that are unaffected by local surf conditions and thus considered representative of open ocean conditions. Despite recent improvements in sea-salt source functions, studies still show significant model errors in specific regions. Using a multiscale model, we investigated the effect of high model resolution (0.1° × 0.1° vs. 1° × 1.4°) upon sea-salt patterns in four stations from the University of Miami Network: Baring Head, Chatam Island, and Invercargill in New Zealand, and Marion Island in the sub-antarctic Indian Ocean. Normalized biases improved from +63.7% to +3.3% and correlation increased from 0.52 to 0.84. The representation of sea/land interfaces, mesoscale circulations, and precipitation with the higher resolution model played a major role in the simulation of annual concentration trends. Our results recommend caution when comparing or constraining global models using surface concentration observations from coastal stations.

  13. Aerosol advection and sea salt events in Genoa, Italy, during the second half of 2005.

    PubMed

    Marenco, Franco; Mazzei, Federico; Prati, Paolo; Gatti, Massimiliano

    2007-05-15

    Atmospheric aerosols in the PM(10) fraction have been simultaneously sampled at three sites in the Genoa urban and suburban area during the second half of 2005, and information on the elemental composition has been gathered through energy dispersive X-ray fluorescence. Thanks to the simultaneous measurements and wind information, a few aerosol transport and transformation processes originated from the nearby sea and in the neighbouring Po Valley have been described. Sea salt concentrations at the three sites were well correlated and often related to Southern sector winds; moreover, by examining the Cl/Na ratio at two sites the time scale for Cl depletion in particulate matter has been estimated as 1-1.5 h for the Genoa atmosphere. During a Northerly gale, excess elemental Si concentrations (peaking more than 4 mug m(-3)) were found at two sites, and were ascribed to an unknown local source. Finally, during an 11-day long 'heat wave' large concentrations for total PM(10), dust and secondary compounds have been found; these large concentrations lead to a number of exceedances of air quality standards, and have been ascribed to advection from the Po Valley.

  14. Measurements of Aerosol Charge and Size Distribution for Graphite, Gold, Palladium, and Silver Nanoparticles

    SciTech Connect

    Simones, Matthew P.; Gutti, Veera R.; Meyer, Ryan M.; Loyalka, Sudarshan K.

    2011-11-01

    The role of charge on aerosol evolution and hence the nuclear source term has been an issue of interest, and there is a need for both experimental techniques and modeling for quantifying this role. Our focus here is on further exploration of a tandem differential mobility analyzer (TDMA) technique to simultaneously measure both the size and charge (positive, negative and neutral) dependent aerosol distributions. We have generated graphite, gold, silver, and palladium nanoparticles (aerosol) using a spark generator. We measure the electrical mobility-size distributions for these aerosols using a TDMA, and from these data we deduce the full charge-size distributions. We observe asymmetry in the particle size distributions for negative and positive charges. This asymmetry could have a bearing on the dynamics of charged aerosols, indicating that the assumption of symmetry for size distributions of negatively and positively charged particles in source term simulations may not be always appropriate. Also, the experimental technique should find applications in measurements of aerosol rate processes that are affected by both particle charge and size (e.g. coagulation, deposition, resuspension), and hence in modeling and simulation of the nuclear source term.

  15. Emissions and Characteristics of Ice Nucleating Particles Associated with Laboratory Generated Nascent Sea Spray Aerosol

    NASA Astrophysics Data System (ADS)

    McCluskey, C. S.; Hill, T. C. J.; Beall, C.; Sultana, C. M.; Moore, K.; Cornwell, G.; Lee, C.; Al-Mashat, H.; Laskina, O.; Trueblood, J.; Grassian, V. H.; Prather, K. A.; Kreidenweis, S. M.; DeMott, P. J.

    2015-12-01

    Accurate emission rates and activity spectra of atmospheric ice nucleating particles (INPs) are required for proper representation of aerosol-cloud interactions in atmospheric modeling studies. However, few investigations have quantified or characterized oceanic INP emissions. In conjunction with the Center for Aerosol Impacts on the Climate and the Environment, we have directly measured changes in INP emissions and properties of INPs from nascent sea spray aerosol (SSA) through the evolution of phytoplankton blooms. Multiple offline and online instruments were used to monitor aerosol chemistry and size, and bulk water characteristics during two phytoplankton bloom experiments. Two methods were utilized to monitor the number concentrations of INPs from 0 to -34 °C: The online CSU continuous flow diffusion chamber (CFDC) and collections processed offline using the CSU ice spectrometer. Single particle analyses were performed on ice crystal residuals downstream of the CFDC, presumed to be INPs, via scanning transmission electron microscopy (STEM) and Raman microspectroscopy. Preliminary results indicate that laboratory-generated nascent SSA corresponds to number concentrations of INPs that are generally consistent with open ocean regions, based on current knowledge. STEM analyses revealed that the sizes of ice crystal residuals that were associated with nascent SSA ranged from 0.3 to 2.5 μm. Raman microspectroscopy analysis of 1 μm sized residuals found a variety of INP identities, including long chain organics, diatom fragments and polysaccharides. Our data suggest that biological processes play a significant role in ocean INP emissions by generating the species and compounds that were identified during these studies.

  16. Lidar Investigation of Aerosol Pollution Distribution near a Coal Power Plant

    NASA Technical Reports Server (NTRS)

    Mitsev, TS.; Kolarov, G.

    1992-01-01

    Using aerosol lidars with high spatial and temporal resolution with the possibility of real-time data interpretation can solve a large number of ecological problems related to the aerosol-field distribution and variation and the structure of convective flows. Significantly less expensive specialized lidars are used in studying anthropogenic aerosols in the planetary boundary layer. Here, we present results of lidar measurements of the mass-concentration field around a coal-fired power plant with intensive local aerosol sources. We studied the pollution evolution as a function of the emission dynamics and the presence of retaining layers. The technique used incorporates complex analysis of three types of lidar mapping: horizontal map of the aerosol field, vertical cross-section map, and a series of profiles along a selected path. The lidar-sounding cycle was performed for the time of atmosphere's quasi-stationarity.

  17. Aerosol generation and distribution system for the Third International Cloud Condensation Nuclei Workshop

    NASA Technical Reports Server (NTRS)

    Katz, U.; Dea, J. Y.

    1981-01-01

    In order to obtain identical samples participating CCN instruments and aerosol characterizing equipment were located along and connected to a 8.2 cm diameter aluminum tube through which the test aerosols were pumped directly from the source at very slight overpressure. Of the total of 29 experiments, 18 were carried out with artificial NaCl or (NH4)2SO4 aerosols. These were generated from salt solutions by pneumatic atomizers of special design to ensure high constancy of the aerosol output concentration. In three experiments with insoluble CCN (AgI, paraffin wax) the aerosols were generated thermally. In some of the tests, an electrostatic classifier was used for narrowing the particle size distributions.

  18. Aerosol size distribution and radiative forcing response to anthropogenically driven historical changes in biogenic secondary organic aerosol formation

    NASA Astrophysics Data System (ADS)

    D'Andrea, S. D.; Acosta Navarro, J. C.; Farina, S. C.; Scott, C. E.; Rap, A.; Farmer, D. K.; Spracklen, D. V.; Riipinen, I.; Pierce, J. R.

    2014-10-01

    Emissions of biogenic volatile organic compounds (BVOC) have changed in the past millennium due to changes in land use, temperature and CO2 concentrations. Recent model reconstructions of BVOC emissions over the past millennium predicted changes in dominant secondary organic aerosol (SOA) producing BVOC classes (isoprene, monoterpenes and sesquiterpenes). The reconstructions predicted that global isoprene emissions have decreased (land-use changes to crop/grazing land dominate the reduction), while monoterpene and sesquiterpene emissions have increased (temperature increases dominate the increases); however, all three show regional variability due to competition between the various influencing factors. These BVOC changes have largely been anthropogenic in nature, and land-use change was shown to have the most dramatic effect by decreasing isoprene emissions. In this work, we use two modeled estimates of BVOC emissions from the years 1000 to 2000 to test the effect of anthropogenic changes to BVOC emissions on SOA formation, global aerosol size distributions, and radiative effects using the GEOS-Chem-TOMAS global aerosol microphysics model. With anthropogenic emissions (e.g. SO2, NOx, primary aerosols) held at present day values and BVOC emissions changed from year 1000 to year 2000 values, decreases in the number concentration of particles of size Dp > 80 nm (N80) of >25% in year 2000 relative to year 1000 were predicted in regions with extensive land-use changes since year 1000 which led to regional increases in direct plus indirect aerosol radiative effect of >0.5 W m-2 in these regions. We test the sensitivity of our results to BVOC emissions inventory, SOA yields and the presence of anthropogenic emissions; however, the qualitative response of the model to historic BVOC changes remains the same in all cases. Accounting for these uncertainties, we estimate millennial changes in BVOC emissions cause a global mean direct effect of between +0.022 and +0.163 W m-2

  19. Primary marine aerosol emissions from the Mediterranean Sea during pre-bloom and oligotrophic conditions: correlations to seawater chlorophyll a from a mesocosm study

    NASA Astrophysics Data System (ADS)

    Schwier, A. N.; Rose, C.; Asmi, E.; Ebling, A. M.; Landing, W. M.; Marro, S.; Pedrotti, M.-L.; Sallon, A.; Iuculano, F.; Agusti, S.; Tsiola, A.; Pitta, P.; Louis, J.; Guieu, C.; Gazeau, F.; Sellegri, K.

    2014-10-01

    The effect of ocean acidification and changing water conditions on primary marine aerosol emissions is not well understood on a regional or a global scale. To investigate this effect as well as the indirect effect on aerosol that changing biogeochemical parameters can have, ~52 m3 pelagic mesocosms were deployed for several weeks in the Mediterranean Sea during both winter pre-bloom and summer oligotrophic conditions and were subjected to various levels of CO2 to simulate the conditions foreseen in this region for the coming decades. After seawater sampling, primary bubble-bursting aerosol experiments were performed using a plunging water jet system to test both chemical and physical aerosol parameters. Comparing results obtained during pre-bloom and oligotrophic conditions, we find the same four log-normal modal diameters (18.5, 37.5, 91.5, 260 nm) describing the aerosol size distribution during both campaigns, yet pre-bloom conditions significantly increased the number fraction of the second (Aitken) mode, with an amplitude correlated to virus-like particles, heterotrophic prokaryotes, TEPs, chlorophyll a and other pigments. Organic fractions determined from κ closure calculations for Dp ~50 nm were much larger during the pre-bloom period (64%) than during the oligotrophic period (38%), and the organic fraction increased as the particle size decreased. Combining data from both campaigns together, strong positive correlations were found between the organic fraction of the aerosol and chlorophyll a concentrations, heterotrophic and autotrophic bacteria abundance, and dissolved organic carbon (DOC) concentrations. As a consequence of the changes in the organic fraction and the size distributions between pre-bloom and oligotrophic periods, we find that the ratio of cloud condensation nuclei (CCN) to condensation nuclei (CN) slightly decreased during the pre-bloom period. The enrichment of the seawater samples with microlayer samples did not have any effect on the

  20. Primary marine aerosol emissions from the Mediterranean Sea during pre-bloom and oligotrophic conditions: correlations to seawater chlorophyll a from a mesocosm study

    NASA Astrophysics Data System (ADS)

    Schwier, A. N.; Rose, C.; Asmi, E.; Ebling, A. M.; Landing, W. M.; Marro, S.; Pedrotti, M.-L.; Sallon, A.; Iuculano, F.; Agusti, S.; Tsiola, A.; Pitta, P.; Louis, J.; Guieu, C.; Gazeau, F.; Sellegri, K.

    2015-07-01

    The effect of ocean acidification and changing water conditions on primary (and secondary) marine aerosol emissions is not well understood on a regional or a global scale. To investigate this effect as well as the indirect effect on aerosol that changing biogeochemical parameters can have, ~ 52 m3 pelagic mesocosms were deployed for several weeks in the Mediterranean Sea during both winter pre-bloom and summer oligotrophic conditions and were subjected to various levels of CO2 to simulate the conditions foreseen in this region for the coming decades. After seawater sampling, primary bubble-bursting aerosol experiments were performed using a plunging water jet system to test both chemical and physical aerosol parameters (10-400 nm). Comparing results obtained during pre-bloom and oligotrophic conditions, we find the same four log-normal modal diameters (18.5 ± 0.6, 37.5 ± 1.4, 91.5 ± 2.0, 260 ± 3.2 nm) describing the aerosol size distribution during both campaigns, yet pre-bloom conditions significantly increased the number fraction of the second (Aitken) mode, with an amplitude correlated to virus-like particles, heterotrophic prokaryotes, TEPs (transparent exopolymeric particles), chlorophyll a and other pigments. Organic fractions determined from kappa closure calculations for the diameter, Dp ~ 50 nm, were much larger during the pre-bloom period (64 %) than during the oligotrophic period (38 %), and the organic fraction decreased as the particle size increased. Combining data from both campaigns together, strong positive correlations were found between the organic fraction of the aerosol and chlorophyll a concentrations, heterotrophic and autotrophic bacteria abundance, and dissolved organic carbon (DOC) concentrations. As a consequence of the changes in the organic fraction and the size distributions between pre-bloom and oligotrophic periods, we find that the ratio of cloud condensation nuclei (CCN) to condensation nuclei (CN) slightly decreased during the

  1. Vertical distribution of tropospheric BrO in the marginal sea ice zone of the Northern Weddell Sea

    NASA Astrophysics Data System (ADS)

    Nasse, Jan-Marcus; Zielcke, Johannes; Lampel, Johannes; Buxmann, Joelle; Frieß, Udo; Platt, Ulrich

    2015-04-01

    The free radical bromine monoxide (BrO) strongly influences the chemistry of the troposphere in Polar regions. During springtime with the return of sunlight after Polar night BrO is released in an autocatalytic reaction mechanism from saline surfaces (bromine explosion). Then BrO affects the oxidative properties of the lower atmosphere and can induce complete depletion of ozone within a matter of days or even hours. In addition, elemental mercury can be oxidized by BrO which makes this toxic compound soluble leading to a deposition into the biosphere. Despite numerous observations of elevated BrO levels in the Polar troposphere, bromine radical sources, as well as the details of the mechanisms leading to bromine explosions and the interactions between atmospheric dynamics and chemistry are not yet completely understood. To improve the understanding of these processes, an accurate determination of the spatio-temporal distribution of BrO is crucial. Here we present measurements of BrO performed during two cruises of the German research ice breaker Polarstern in the marginal sea ice zone of the Antarctic Weddell Sea between June and October 2013 when four major periods with elevated BrO concentrations and simultaneous ozone depletion occurred. The events were observed by (1) a ship-based Multi AXis Differential Absorption Spectroscopy (MAX-DOAS) instrument on Polarstern and (2) a compact MAX-DOAS instrument operated on a helicopter. Several flights were performed in the boundary layer as well as in the free troposphere up to altitudes of 2300 m on days with elevated BrO levels. Vertical profiles of aerosol extinction and BrO concentrations were retrieved for both instruments using our HEIPRO (HEIdelberg Profile) retrieval algorithm based on optimal estimation. Elevated BrO levels in the time series from ship-borne measurements show a strong correlation to southerly wind directions indicating transport from sea ice areas. Maximum retrieved BrO mixing ratios at ground

  2. Global modelling of direct and indirect effects of sea spray aerosol using a source function encapsulating wave state

    NASA Astrophysics Data System (ADS)

    Partanen, A.-I.; Dunne, E. M.; Bergman, T.; Laakso, A.; Kokkola, H.; Ovadnevaite, J.; Sogacheva, L.; Baisnée, D.; Sciare, J.; Manders, A.; O'Dowd, C.; de Leeuw, G.; Korhonen, H.

    2014-11-01

    Recently developed parameterizations for the sea spray aerosol source flux, encapsulating wave state, and its organic fraction were incorporated into the aerosol-climate model ECHAM-HAMMOZ to investigate the direct and indirect radiative effects of sea spray aerosol particles. Our simulated global sea salt emission of 805 Tg yr-1 (uncertainty range 378-1233 Tg yr-1) was much lower than typically found in previous studies. Modelled sea salt and sodium ion concentrations agreed relatively well with measurements in the smaller size ranges at Mace Head (annual normalized mean model bias -13% for particles with vacuum aerodynamic diameter Dva < 1 μm), Point Reyes (-29% for particles with aerodynamic diameter Da < 2.5 μm) and Amsterdam Island (-52% for particles with Da < 1 μm) but the larger sizes were overestimated (899% for particles with 2.5 μm < Da < 10 μm) at Amsterdam Island. This suggests that at least the high end of the previous estimates of sea spray mass emissions is unrealistic. On the other hand, the model clearly underestimated the observed concentrations of organic or total carbonaceous aerosol at Mace Head (-82%) and Amsterdam Island (-68%). The large overestimation (212%) of organic matter at Point Reyes was due to the contribution of continental sources. At the remote Amsterdam Island site, the organic concentration was underestimated especially in the biologically active months, suggesting a need to improve the parameterization of the organic sea spray fraction. Globally, the satellite-retrieved AOD over the oceans, using PARASOL data, was underestimated by the model (means over ocean 0.16 and 0.10, respectively); however, in the pristine region around Amsterdam Island the measured AOD fell well within the simulated uncertainty range. The simulated sea spray aerosol contribution to the indirect radiative effect was positive (0.3 W m-2), in contrast to previous studies. This positive effect was ascribed to the tendency of sea salt aerosol to

  3. Global modelling of direct and indirect effects of sea spray aerosol using a source function encapsulating wave state

    NASA Astrophysics Data System (ADS)

    Partanen, A.-I.; Dunne, E. M.; Bergman, T.; Laakso, A.; Kokkola, H.; Ovadnevaite, J.; Sogacheva, L.; Baisnée, D.; Sciare, J.; Manders, A.; O'Dowd, C.; de Leeuw, G.; Korhonen, H.

    2014-02-01

    Recently developed parameterizations for the sea spray aerosol source flux, encapsulating wave state, and its organic fraction were incorporated into the aerosol-climate model ECHAM-HAMMOZ to investigate the direct and indirect radiative effects of sea spray aerosol particles. Our simulated global sea salt emission of 805 Tg yr-1 (uncertainty range 378-1233 Tg yr-1) was much lower than typically found in previous studies. Modelled sea salt and sodium ion concentrations agreed relatively well with measurements in the smaller size ranges at Mace Head (annual normalized mean model bias -13% for particles with vacuum aerodynamic diameter Dva < 1 μm), Point Reyes (-29% for particles with aerodynamic diameter Da < 2.5 μm) and Amsterdam Island (-52% for particles with Da < 1 μm) but the larger sizes were overestimated (899% for particles with 2.5 μm sea spray mass emissions is unrealistic. On the other hand, the model clearly underestimated the observed concentrations of organic or total carbonaceous aerosol at Mace Head (-82%) and Amsterdam Island (-68%). The large overestimation (212%) of organic matter at Point Reyes was due to the contribution of continental sources. At the remote Amsterdam Island site, the organic concentration was underestimated especially in the biologically active months, suggesting a need to improve the parameterization of the organic sea spray fraction. Globally, the satellite-retrieved AOD over the oceans, using PARASOL data, was underestimated by the model (means over ocean 0.16 and 0.10, respectively); however, in the pristine region around Amsterdam Island the measured AOD fell well within the simulated uncertainty range. The simulated sea spray aerosol contribution to the indirect radiative effect was positive (0.3 W m-2), in contrast to previous studies. This positive effect was ascribed to the tendency of sea salt aerosol to

  4. [Determination of the retrieval arithmetic of aerosol size distribution measured by DOAS].

    PubMed

    Si, Fu-qi; Xie, Pin-hua; Liu, Jian-guo; Zhang, Yu-jun; Liu, Wen-qing; Hiroaki, Kuze; Nobuo, Takeuchi

    2008-10-01

    Atmospheric aerosol is not only an important factor for the change in global climate, but also a polluting matter. Moreover, aerosol plays a main role in chemical reaction of polluting gases. Determination of aerosol has become an important re- search in the study of atmospheric environment. Differential optical absorption spectroscopy (DOAS) is a very useful technique that allows quantitative measurement of atmospheric trace gas concentrations based on their fingerprint absorption. It also can be used to retrieve aerosol extinction coefficient. In the present work, the method of determination of aerosol size distribution measured by flash DOAS is described, and the arithmetic based on Monte-Carlo is the emphasis. By comparison with the concentration of PM10, visibility and Angstrom wavelength exponent, a good correlation can be found. Application of DOAS in aerosol field not only provides a novel method for aerosol detection, but also extends the field of application of DOAS technology. Especially, aerosol DOAS plays an important role in the study of atmospheric chemistry.

  5. [Determination of the retrieval arithmetic of aerosol size distribution measured by DOAS].

    PubMed

    Si, Fu-qi; Xie, Pin-hua; Liu, Jian-guo; Zhang, Yu-jun; Liu, Wen-qing; Hiroaki, Kuze; Nobuo, Takeuchi

    2008-10-01

    Atmospheric aerosol is not only an important factor for the change in global climate, but also a polluting matter. Moreover, aerosol plays a main role in chemical reaction of polluting gases. Determination of aerosol has become an important re- search in the study of atmospheric environment. Differential optical absorption spectroscopy (DOAS) is a very useful technique that allows quantitative measurement of atmospheric trace gas concentrations based on their fingerprint absorption. It also can be used to retrieve aerosol extinction coefficient. In the present work, the method of determination of aerosol size distribution measured by flash DOAS is described, and the arithmetic based on Monte-Carlo is the emphasis. By comparison with the concentration of PM10, visibility and Angstrom wavelength exponent, a good correlation can be found. Application of DOAS in aerosol field not only provides a novel method for aerosol detection, but also extends the field of application of DOAS technology. Especially, aerosol DOAS plays an important role in the study of atmospheric chemistry. PMID:19123420

  6. Atmospheric correction of ocean color imagery: use of the junge power-law aerosol size distribution with variable refractive index to handle aerosol absorption.

    PubMed

    Chomko, R M; Gordon, H R

    1998-08-20

    When strongly absorbing aerosols are present in the atmosphere, the usual two-step procedure of processing ocean color data-(1) atmospheric correction to provide the water-leaving reflectance (rho(w)), followed by (2) relating rho(w) to the water constituents-fails and simultaneous estimation of the ocean and aerosol optical properties is necessary. We explore the efficacy of using a simple model of the aerosol-a Junge power-law size distribution consisting of homogeneous spheres with arbitrary refractive index-in a nonlinear optimization procedure for estimating the relevant oceanic and atmospheric parameters for case 1 waters. Using simulated test data generated from more realistic aerosol size distributions (sums of log-normally distributed components with different compositions), we show that the ocean's pigment concentration (C) can be retrieved with good accuracy in the presence of weakly or strongly absorbing aerosols. However, because of significant differences in the scattering phase functions for the test and power-law distributions, large error is possible in the estimate of the aerosol optical thickness. The positive result for C suggests that the detailed shape of the aerosol-scattering phase function is not relevant to the atmospheric correction of ocean color sensors. The relevant parameters are the aerosol single-scattering albedo and the spectral variation of the aerosol optical depth. We argue that the assumption of aerosol sphericity should not restrict the validity of the algorithm and suggest an avenue for including colored aerosols, e.g., wind-blown dust, in the procedure. A significant advantage of the new approach is that realistic multicomponent aerosol models are not required for the retrieval of C.

  7. Vertical distribution of aerosols in the vicinity of Mexico City during MILAGRO-2006 Campaign

    SciTech Connect

    Lewandowski, P.A.; Kleinman, L.; Eichinger, W. E.; Holder, H.; Prueger, J.; Wang, J.

    2010-02-01

    On 7 March 2006, a mobile, ground-based, vertical pointing, elastic lidar system made a North-South transect through the Mexico City basin. Column averaged, aerosol size distribution (ASD) measurements were made on the ground concurrently with the lidar measurements. The ASD ground measurements allowed calculation of the column averaged mass extinction efficiency (MEE) for the lidar system (1064 nm). The value of column averaged MEE was combined with spatially resolved lidar extinction coefficients to produce total aerosol mass concentration estimates with the resolution of the lidar (1.5 m vertical spatial and 1 s temporal). Airborne ASD measurements from DOE G-1 aircraft made later in the day on 7 March 2006, allowed the evaluation of the assumptions of constant ASD with height and time used for estimating the column averaged MEE. The results showed that the aerosol loading within the basin is about twice what is observed outside of the basin. The total aerosol base concentrations observed in the basin are of the order of 200 {mu}g/m{sup 3} and the base levels outside are of the order of 100 {mu}g/m{sup 3}. The local heavy traffic events can introduce aerosol levels near the ground as high as 900 {mu}g/m{sup 3}. The article presents the methodology for estimating aerosol mass concentration from mobile, ground-based lidar measurements in combination with aerosol size distribution measurements. An uncertainty analysis of the methodology is also presented.

  8. An inexpensive active optical remote sensing instrument for assessing aerosol distributions.

    PubMed

    Barnes, John E; Sharma, Nimmi C P

    2012-02-01

    Air quality studies on a broad variety of topics from health impacts to source/sink analyses, require information on the distributions of atmospheric aerosols over both altitude and time. An inexpensive, simple to implement, ground-based optical remote sensing technique has been developed to assess aerosol distributions. The technique, called CLidar (Charge Coupled Device Camera Light Detection and Ranging), provides aerosol altitude profiles over time. In the CLidar technique a relatively low-power laser transmits light vertically into the atmosphere. The transmitted laser light scatters off of air molecules, clouds, and aerosols. The entire beam from ground to zenith is imaged using a CCD camera and wide-angle (100 degree) optics which are a few hundred meters from the laser. The CLidar technique is optimized for low altitude (boundary layer and lower troposphere) measurements where most aerosols are found and where many other profiling techniques face difficulties. Currently the technique is limited to nighttime measurements. Using the CLidar technique aerosols may be mapped over both altitude and time. The instrumentation required is portable and can easily be moved to locations of interest (e.g. downwind from factories or power plants, near highways). This paper describes the CLidar technique, implementation and data analysis and offers specifics for users wishing to apply the technique for aerosol profiles.

  9. A new source of Southern Ocean and Antarctic aerosol from tropospheric polar cell chemistry of sea ice emissions

    NASA Astrophysics Data System (ADS)

    Humphries, R. S.; Klekociuk, A. R.; Schofield, R.; Robinson, A. D.; Harris, N. R. P.; Keywood, M.; Ward, J.; Galbally, I.; Molloy, S.; Thomas, A.; Wilson, S. R.

    2014-12-01

    The Antarctic region is a pristine environment with minimal anthropogenic influence. Aerosol measurements in this environment allow the study of natural aerosols and polar atmospheric dynamics. Measurements in this region have been limited primarily to continental and coastal locations where permanent stations exist, with a handful of measurements in the sea ice region. The MAPS campaign (Measurements of Aerosols and Precursors during SIPEXII) occurred as part of SIPEX II (Sea Ice Physics and Ecosystems eXperiment II) voyage in Spring, 2012, and produced the first Antarctic pack-ice focused aerosol dataset aimed at characterizing new particle formation processes off the coast of East Antarctica (~65°S, 120°E). Numerous atmospheric parameters and species were measured, including the number of aerosol particles in the 3-10 nm size range, the range associated with nucleating particle formation. A latitudinal transect through the sea ice identified the Polar Front from sudden changes in nucleating particle concentrations, averaging 51cm-3 north of the front in the Ferrel cell, and 766 cm-3 south of the front, in the Polar cell region. The Polar Front location was also confirmed by meteorological and back-trajectory data. Background aerosol populations in the Polar cell fluctuated significantly but displayed no growth indicators, suggesting transport. Back-trajectories revealed that air parcels often descended from the free-troposphere within the previous 24-48 hrs. It is proposed that particle formation occurs in the free troposphere from precursors uplifted at the polar front region which, being a sea-ice/ocean region, is a significant precursor source. After tropospheric formation, populations descending at the poles are transported northward and reach the sea ice surface, missing continental stations. Current measurements of Antarctic aerosol suggest very low loading which may be explained by these circulation patterns and may underestimate total regional loading

  10. Assessment of the aerosol distribution over Indian subcontinent in CMIP5 models

    NASA Astrophysics Data System (ADS)

    Sanap, S. D.; Ayantika, D. C.; Pandithurai, G.; Niranjan, K.

    2014-04-01

    This paper examines the aerosol distribution over Indian subcontinent as represented in 21 models from Coupled Model Inter-comparison Project Phase 5 (CMIP5) simulations, wherein model simulated aerosol optical depth (AOD) is compared with Moderate Resolution Imaging Spectro-radiometer (MODIS) satellite observations. The objective of the study is to provide an assessment of the capability of various global models, participating in CMIP5 project, in capturing the realistic spatial and temporal distribution of aerosol species over the Indian subcontinent. Results from our analysis show that majority of the CMIP5 models (excepting HADGEM2-ES, HADGEM2-CC) seriously underestimates the spatio-temporal variability of aerosol species over the Indian subcontinent, in particular over Indo-Gangetic Plains (IGP). Since IGP region is dominated by anthropogenic activities, high population density, and wind driven transport of dust and other aerosol species, MODIS observations reveal high AOD values over this region. Though the representation of black carbon (BC) loading in many models is fairly good, the dust loading is observed to be significantly low in majority of the models. The presence of pronounced dust activity over northern India and dust being one of the major constituent of aerosol species, the biases in dust loading has a great impact on the AOD of that region. We found that considerable biases in simulating the 850 hPa wind field (which plays important role in transport of dust from adjacent deserts) would be the possible reason for poor representation of dust AOD and in turn total AOD over Indian region in CMIP5 models. In addition, aerosol radiative forcing (ARF) underestimated/overestimated in most of the models. However, spatial distribution of ARF in multi-model ensemble mean is comparable reasonably well with observations with bias in magnitudes. This analysis emphasizes the fundamental need to improve the representation of aerosol species in current state of

  11. The distribution of iodide at the sea surface.

    PubMed

    Chance, Rosie; Baker, Alex R; Carpenter, Lucy; Jickells, Tim D

    2014-08-01

    Recent studies have highlighted the impact of sea surface iodide concentrations on the deposition of ozone to the sea surface and the sea to air flux of reactive iodine. The use of models to predict this flux demands accurate, spatially distributed sea surface iodide concentrations, but to date, the observational data required to support this is sparse and mostly arises from independent studies conducted on small geographical and temporal scales. We have compiled the available measurements of sea surface iodide to produce a data set spanning latitudes from 69°S to 66°N, which reveals a coherent, large scale distribution pattern, with highest concentrations observed in tropical waters. Relationships between iodide concentration and more readily available parameters (chlorophyll, nitrate, sea surface temperature, salinity, mixed layer depth) are evaluated as tools to predict iodide concentration. Of the variables tested, sea surface temperature is the strongest predictor of iodide concentration. Nitrate was also strongly inversely associated with iodide concentration, but chlorophyll-a was not.

  12. Sensitivity of aerosol-induced effects on numerically simulated squall lines to the vertical distribution of aerosols

    NASA Astrophysics Data System (ADS)

    Lebo, Z. J.

    2013-12-01

    The sensitivity of aerosol-induced enhancement of convective strength and precipitation to the vertical distribution is analyzed in the context of numerically simulated squall lines. Recent investigations have hypothesized and demonstrated that an increase in an aerosol loading may lead to enhanced vertical updrafts and potentially more precipitation in a variety of deep convective systems. One of the generally accepted hypotheses for such an enhancement in convective strength suggests that the predominant effect of an increase in aerosol loading is related to enhanced latent heat release in the mid to upper levels of the convective cores. This enhancement has been attributed to an increase in supercooled liquid water that tends to exist in clouds formed in more polluted environments and it is suggested that this water is lofted from below the freezing level to the mixed-phase region of the cloud where the latent heating effects are maximized. However, deep convective cores are quite strong and so a reduction in cloud droplet size due to enhanced aerosol number concentration (which reduces the terminal fall speed) ought to have a negligible effect on the trajectory of the droplets (since the updraft velocity is much larger than the terminal fall speed). Thus, it should be expected that low-level aerosol pollution would have little to no effect on latent heating rates aloft since the droplets will end up in the mixed-phase region regardless of size. Moreover, more recent investigations have shown that aerosol perturbations, especially in squall lines, can lead to less intense cold pools and thus a more optimal state according to RKW theory. Numerical simulations of idealized squall lines are performed to specifically analyze the sensitivity of the aforementioned effects to the vertical distribution of aerosols. The simulations suggest that low-level air tends to either be detrained at the bottom of the convective cores or remains in the convective cores throughout

  13. Updating sea spray aerosol emissions in the Community Multiscale Air Quality (CMAQ) model version 5.0.2

    EPA Science Inventory

    Sea spray aerosols (SSAs) impact the particle mass concentration and gas-particle partitioning in coastal environments, with implications for human and ecosystem health. Model evaluations of SSA emissions have mainly focused on the global scale, but regional-scale evaluations are...

  14. The Remote Sensing of Mineral Aerosols and Their Impact on Phytoplankton Productivity using Sea WiFS

    NASA Technical Reports Server (NTRS)

    Stegmann, Petra M.

    1998-01-01

    The main objective of this proposal was to use SeaWiFs data to study the relationship between aerosols found in aeollan dust and photosynthesis of phytoplankton in open ocean surface waters. This project was a collaborative effort between myself and Dr. Neil Tindale at Texas A&M University and followed on our earlier funded proposal which had been designed as a proof-of-concept study to determine if ocean color sensors such as the Coastal Zone Color Scanner (CZCS) could be used to detect and map large-scale mineral aerosol plumes. Despite the large spatial and temporal gaps inherent in the CZCS data coverage, our results from this initial study indicated that an ocean color sensor could indeed be used to detect aerosols. These encouraging results led us to propose in this proposal the use of SeaWiFS data to study mineral aerosol transport and its impact on phytoplankton production. This proposal orignally intended to make use of SeaWiFS images, but as the launch delay of SeaWiFS dragged on, we had to make do with other satellite data sets. Thus, the focus of this proposal became the CSCS image archive instead. I detail my results and accomplishments with this data set.

  15. [Distribution of dissolved organic carbon in the Bohai Sea and Yellow Sea in spring].

    PubMed

    Ding, Yan-Yan; Zhang, Chuan-Song; Shi, Xiao-Yong; Shang, Rong-Ning

    2012-01-01

    Based on the data from cruises that carried out in the Yellow Sea and Bohai Sea from April to May, 2010, the horizontal distribution of DOC was studied. And the influencing factors were preliminary discussed. The results showed that the concentration of DOC in the Yellow Sea and Bohai Sea ranged from 0.96 to 4.71 mg x L(-1) in spring and the average content was 2.27 mg x L(-1). In horizontal distribution, the highest DOC content appeared in the coastal zones both in the south and the north and it tended to decrease toward the offshore in central section on the whole. The highest DOC value was in the nearshore in the western of Bohai Sea and eastern of Shandong Peninsula which was mainly affected by the terrestrial inputs and the offshore current, especially in the nearshore of the western of Bohai Sea, the highest DOC content was 4.71 mg x L(-1). The second highest DOC value was in the Northeast of Yangtze River Estuary which was mainly affected by the Yangtze River Diluted Water (YRDW). However, the low DOC content was mainly found in open seas in the central of the South Yellow Sea, and the DOC value was lower than 1.50 mg x L(-1).

  16. [Distribution and air-sea fluxes of methane in the Yellow Sea and the East China Sea in the spring].

    PubMed

    Cao, Xing-Peng; Zhang, Gui-Ling; Ma, Xiao; Zhang, Guo-Ling; Liu, Su-Mei

    2013-07-01

    A survey was carried out in the Yellow Sea and the East China Sea from March 17 to April 06 of 2011. Dissolved CH4 in various depths were measured and sea-to-air fluxes were estimated. Methane concentrations in surface and bottom waters ranged between 2.39-29.67 nmol x L(-1) and 2.63-30.63 nmol x L(-1), respectively. Methane concentrations in bottom waters were slightly higher than those in surface waters, suggesting the existence of methane source in bottom waters or sediments. The horizontal distribution of dissolved CH4 showed a decrease from the river mouth to the open sea, and was influenced by the freshwater discharge and the Kuroshio intrusion. Surface methane saturations ranged from 93%-1 038%. Sea to air CH4 fluxes were (2.85 +/- 5.11) micromol x (m2 x d)(-1) (5.18 +/- 9.99) micromol x (m2 x d)(-1) respectively, calculated using the Liss and Merlivat (LM86), the Wanninkhof (W92) relationships and in situ wind speeds, and estimated emission rates of methane from the East China Sea and the Yellow Sea range from 7.05 x 10(-2) - 12.0 x 10(-2) Tg x a(-1) and 1.17 x 10(-2) - 2.20 x 10(-2) Tg x a(-1), respectively. The Yellow Sea and East China Sea are the net sources of atmospheric methane in the spring.

  17. Species distribution models of tropical deep-sea snappers.

    PubMed

    Gomez, Céline; Williams, Ashley J; Nicol, Simon J; Mellin, Camille; Loeun, Kim L; Bradshaw, Corey J A

    2015-01-01

    Deep-sea fisheries provide an important source of protein to Pacific Island countries and territories that are highly dependent on fish for food security. However, spatial management of these deep-sea habitats is hindered by insufficient data. We developed species distribution models using spatially limited presence data for the main harvested species in the Western Central Pacific Ocean. We used bathymetric and water temperature data to develop presence-only species distribution models for the commercially exploited deep-sea snappers Etelis Cuvier 1828, Pristipomoides Valenciennes 1830, and Aphareus Cuvier 1830. We evaluated the performance of four different algorithms (CTA, GLM, MARS, and MAXENT) within the BIOMOD framework to obtain an ensemble of predicted distributions. We projected these predictions across the Western Central Pacific Ocean to produce maps of potential deep-sea snapper distributions in 32 countries and territories. Depth was consistently the best predictor of presence for all species groups across all models. Bathymetric slope was consistently the poorest predictor. Temperature at depth was a good predictor of presence for GLM only. Model precision was highest for MAXENT and CTA. There were strong regional patterns in predicted distribution of suitable habitat, with the largest areas of suitable habitat (> 35% of the Exclusive Economic Zone) predicted in seven South Pacific countries and territories (Fiji, Matthew & Hunter, Nauru, New Caledonia, Tonga, Vanuatu and Wallis & Futuna). Predicted habitat also varied among species, with the proportion of predicted habitat highest for Aphareus and lowest for Etelis. Despite data paucity, the relationship between deep-sea snapper presence and their environments was sufficiently strong to predict their distribution across a large area of the Pacific Ocean. Our results therefore provide a strong baseline for designing monitoring programs that balance resource exploitation and conservation planning, and

  18. Species Distribution Models of Tropical Deep-Sea Snappers

    PubMed Central

    Gomez, Céline; Williams, Ashley J.; Nicol, Simon J.; Mellin, Camille; Loeun, Kim L.; Bradshaw, Corey J. A.

    2015-01-01

    Deep-sea fisheries provide an important source of protein to Pacific Island countries and territories that are highly dependent on fish for food security. However, spatial management of these deep-sea habitats is hindered by insufficient data. We developed species distribution models using spatially limited presence data for the main harvested species in the Western Central Pacific Ocean. We used bathymetric and water temperature data to develop presence-only species distribution models for the commercially exploited deep-sea snappers Etelis Cuvier 1828, Pristipomoides Valenciennes 1830, and Aphareus Cuvier 1830. We evaluated the performance of four different algorithms (CTA, GLM, MARS, and MAXENT) within the BIOMOD framework to obtain an ensemble of predicted distributions. We projected these predictions across the Western Central Pacific Ocean to produce maps of potential deep-sea snapper distributions in 32 countries and territories. Depth was consistently the best predictor of presence for all species groups across all models. Bathymetric slope was consistently the poorest predictor. Temperature at depth was a good predictor of presence for GLM only. Model precision was highest for MAXENT and CTA. There were strong regional patterns in predicted distribution of suitable habitat, with the largest areas of suitable habitat (> 35% of the Exclusive Economic Zone) predicted in seven South Pacific countries and territories (Fiji, Matthew & Hunter, Nauru, New Caledonia, Tonga, Vanuatu and Wallis & Futuna). Predicted habitat also varied among species, with the proportion of predicted habitat highest for Aphareus and lowest for Etelis. Despite data paucity, the relationship between deep-sea snapper presence and their environments was sufficiently strong to predict their distribution across a large area of the Pacific Ocean. Our results therefore provide a strong baseline for designing monitoring programs that balance resource exploitation and conservation planning, and

  19. Species distribution models of tropical deep-sea snappers.

    PubMed

    Gomez, Céline; Williams, Ashley J; Nicol, Simon J; Mellin, Camille; Loeun, Kim L; Bradshaw, Corey J A

    2015-01-01

    Deep-sea fisheries provide an important source of protein to Pacific Island countries and territories that are highly dependent on fish for food security. However, spatial management of these deep-sea habitats is hindered by insufficient data. We developed species distribution models using spatially limited presence data for the main harvested species in the Western Central Pacific Ocean. We used bathymetric and water temperature data to develop presence-only species distribution models for the commercially exploited deep-sea snappers Etelis Cuvier 1828, Pristipomoides Valenciennes 1830, and Aphareus Cuvier 1830. We evaluated the performance of four different algorithms (CTA, GLM, MARS, and MAXENT) within the BIOMOD framework to obtain an ensemble of predicted distributions. We projected these predictions across the Western Central Pacific Ocean to produce maps of potential deep-sea snapper distributions in 32 countries and territories. Depth was consistently the best predictor of presence for all species groups across all models. Bathymetric slope was consistently the poorest predictor. Temperature at depth was a good predictor of presence for GLM only. Model precision was highest for MAXENT and CTA. There were strong regional patterns in predicted distribution of suitable habitat, with the largest areas of suitable habitat (> 35% of the Exclusive Economic Zone) predicted in seven South Pacific countries and territories (Fiji, Matthew & Hunter, Nauru, New Caledonia, Tonga, Vanuatu and Wallis & Futuna). Predicted habitat also varied among species, with the proportion of predicted habitat highest for Aphareus and lowest for Etelis. Despite data paucity, the relationship between deep-sea snapper presence and their environments was sufficiently strong to predict their distribution across a large area of the Pacific Ocean. Our results therefore provide a strong baseline for designing monitoring programs that balance resource exploitation and conservation planning, and

  20. Particle size distribution of n-alkanes nda Pb-210 in aerosols off the coast of Peru

    NASA Astrophysics Data System (ADS)

    Schneider, J. K.; Gagosian, R. B.; Cochran, J. K.; Trull, T. W.

    1983-08-01

    The results of particle size distributions measurements of aliphatic hydrocarbons and Pb-210 in aerosols in the upwelling zone off the Peruvian coast are reported. The data were taken as part of the Sea/Air Exchange Program (Searex) using cascade impactor samples on ships cruising 10-100 km off the coast. The samplers were situated on masts on the bow of the ship, which was steered into the wind, with samples taken only when the wind speeds exceeded 5 m/sec. The dominant aliphatic hydrocarbon fraction was n-alkanes above C20, and n-alkane concentrations were calculated as a function of the carbon number. Increasing Pb-210 concentrations were observed with decreasing particle size, a similar situation to that of the n-alkanes. It is suggested that the particle size distribution characteristics are due to fossil fuel combustion and gas-particle partitioning of the n-alkanes.

  1. Assessment of aerosol optics, microphysics, and transport process of biomass-burning haze over northern SE Asia: 7-SEAS AERONET observations

    NASA Astrophysics Data System (ADS)

    Wang, S.; Giles, D. M.; Eck, T. F.; Lin, N.; Tsay, S.; Holben, B. N.

    2013-12-01

    Initiated in 2007, the Seven South East Asian Studies (7-SEAS) is aimed to facilitate an interdisciplinary research on the aerosol environment in SE Asia (SEA) as a whole, promote international collaboration, and further enhance scientific understanding of the impact of biomass burning on clouds, atmospheric radiation, hydrological cycle, and region climates. One of the key measurements proposed in the 7-SEAS is the NASA/AERONET (AErosol RObotic NETwork) observation, which provides helpful information on columnar aerosol optical properties and allows us consistently to examine biomass-burning aerosols across northern SEA from ground-based remote-sensing point of view. In this presentation, we will focus on the two 7-SEAS field deployments, i.e. the 2012 Son La Experiment and the 2013 BASELInE (Biomass-burning Aerosols & Stratocumulus Environment: Lifecycles and Interactions Experiment). We analyze the daytime variation of aerosol by using consistent measurements from 15 of AERONET sites over Indochina, the South China Sea, and Taiwan. Spatiotemporal characteristics of aerosol optical properties (e.g., aerosol optical depth (AOD), fine/coarse mode AOD, single-scattering albedo, asymmetry factor) will be discussed. Strong diurnal variation of aerosol optical properties was observed to be attributed to planetary boundary layer (PBL) dynamics. A comparison between aerosol loading (i.e. AOD) and surface PM2.5 concentration will be presented. Our results demonstrate that smoke aerosols emitted from agriculture burning that under certain meteorological conditions can degrade regional air quality 3000 km from the source region, with additional implications for aerosol radiative forcing and regional climate change over northern SE Asia.

  2. Fractionation of sulfur isotopes during heterogeneous oxidation of SO2 on sea salt aerosol: a new tool to investigate non-sea salt sulfate production in the marine boundary layer

    NASA Astrophysics Data System (ADS)

    Harris, E.; Sinha, B.; Hoppe, P.; Foley, S.; Borrmann, S.

    2012-05-01

    The oxidation of SO2 to sulfate on sea salt aerosols in the marine environment is highly important because of its effect on the size distribution of sulfate and the potential for new particle nucleation from H2SO4 (g). However, models of the sulfur cycle are not currently able to account for the complex relationship between particle size, alkalinity, oxidation pathway and rate - which is critical as SO2 oxidation by O3 and Cl catalysis are limited by aerosol alkalinity, whereas oxidation by hypohalous acids and transition metal ions can continue at low pH once alkalinity is titrated. We have measured 34S/32S fractionation factors for SO2 oxidation in sea salt, pure water and NaOCl aerosol, as well as the pH dependency of fractionation. Oxidation of SO2 by NaOCl aerosol was extremely efficient, with a reactive uptake coefficient of ≈0.5, and produced sulfate that was enriched in 32S with αOCl = 0.9882±0.0036 at 19 °C. Oxidation on sea salt aerosol was much less efficient than on NaOCl aerosol, suggesting alkalinity was already exhausted on the short timescale of the experiments. Measurements at pH = 2.1 and 7.2 were used to calculate fractionation factors for each step from SO2(g) → multiple steps → SOOCl2-. Oxidation on sea salt aerosol resulted in a lower fractionation factor than expected for oxidation of SO32- by O3 (αseasalt = 1.0124±0.0017 at 19 °C). Comparison of the lower fractionation during oxidation on sea salt aerosol to the fractionation factor for high pH oxidation shows HOCl contributed 29% of S(IV) oxidation on sea salt in the short experimental timescale, highlighting the potential importance of hypohalous acids in the marine environment. The sulfur isotope fractionation factors measured in this study allow differentiation between the alkalinity-limited pathways - oxidation by O3 and by Cl catalysis (α34 = 1.0163±0.0018 at 19 °C in pure water or 1.0199±0.0024 at pH = 7.2) - which favour the heavy isotope, and the alkalinity non

  3. Aerosol Size Distribution Determined From Multiple Field-Of-View Lidar

    NASA Astrophysics Data System (ADS)

    Liu, Y.; Yabuki, M.; Tsuda, T.; Uesugi, T.

    2014-12-01

    Knowledge of aerosol size distribution is essential for its influence on atmosphere and human health, especially for small particles because they are able to penetrate lung tissues, thus increasing the risk of bronchitis or lung diseases. Lidar as an active optical remote sensing technique is effective for monitoring aerosols with high temporal and spatial variations. Particles with diameters comparable to the detecting light wavelength have been effectively detected by using UV, VIS, and near-IR wavelengths. However, to quantitatively estimate the shape of the particle size distribution, more information is required with respect to sub-micrometer and smaller particles. Conventional lidar employs tiny field-of-view (FOV) to detect single scatter reflected from aerosols in the direction opposite to incident light. However, the complicated reflection on the path of laser causes multiple scatter which contains also the size distribution information of aerosols. In this study, a UV Lidar with multiple FOV receiver was used for detecting such multiple scattering effects in order to obtain more quantitative information related to particle size distribution. The FOV of Lidar receiver was program controlled in a range from 0.1 mrad to 12.4 mrad. The pacific retrieval method for aerosol size distribution using this feature and field measurement results will be introduced in the presentation.

  4. Relationships linking primary production, sea ice melting, and biogenic aerosol in the Arctic

    NASA Astrophysics Data System (ADS)

    Becagli, S.; Lazzara, L.; Marchese, C.; Dayan, U.; Ascanius, S. E.; Cacciani, M.; Caiazzo, L.; Di Biagio, C.; Di Iorio, T.; di Sarra, A.; Eriksen, P.; Fani, F.; Giardi, F.; Meloni, D.; Muscari, G.; Pace, G.; Severi, M.; Traversi, R.; Udisti, R.

    2016-07-01

    This study examines the relationships linking methanesulfonic acid (MSA, arising from the atmospheric oxidation of the biogenic dimethylsulfide, DMS) in atmospheric aerosol, satellite-derived chlorophyll a (Chl-a), and oceanic primary production (PP), also as a function of sea ice melting (SIM) and extension of the ice free area in the marginal ice zone (IF-MIZ) in the Arctic. MSA was determined in PM10 samples collected over the period 2010-2012 at two Arctic sites, Ny Ålesund (78.9°N, 11.9°E), Svalbard islands, and Thule Air Base (76.5°N, 68.8°W), Greenland. PP is calculated by means of a bio-optical, physiologically based, semi-analytical model in the potential source areas located in the surrounding oceanic regions (Barents and Greenland Seas for Ny Ålesund, and Baffin Bay for Thule). Chl-a peaks in May in the Barents sea and in the Baffin Bay, and has maxima in June in the Greenland sea; PP follows the same seasonal pattern of Chl-a, although the differences in absolute values of PP in the three seas during the blooms are less marked than for Chl-a. MSA shows a better correlation with PP than with Chl-a, besides, the source intensity (expressed by PP) is able to explain more than 30% of the MSA variability at the two sites; the other factors explaining the MSA variability are taxonomic differences in the phytoplanktonic assemblages, and transport processes from the DMS source areas to the sampling sites. The taxonomic differences are also evident from the slopes of the correlation plots between MSA and PP: similar slopes (in the range 34.2-36.2 ng m-3of MSA/(gC m-2 d-1)) are found for the correlation between MSA at Ny Ålesund and PP in Barents Sea, and between MSA at Thule and PP in the Baffin Bay; conversely, the slope of the correlation between MSA at Ny Ålesund and PP in the Greenland Sea in summer is smaller (16.7 ng m-3of MSA/(gC m-2 d-1)). This is due to the fact that DMS emission from the Barents Sea and Baffin Bay is mainly related to the MIZ

  5. On the Vertical Distribution of Aerosols and Long-Range Transport Inferred from Calipso Satellite Observations

    NASA Astrophysics Data System (ADS)

    Trepte, Charles; Winker, David; Kittaka, Chieko

    Knowledge on the long-range transport and evolution of aerosols originating from natural and anthropogenic sources is important for understanding their impact on the composition of the atmosphere and the climate system. Over the past several decades a wealth of information on aerosol distributions has been obtained from ground-based instrument networks, dedicated field experiments, and passive remote sensing satellite instruments that has helped to establish the primary aerosol transport pathways over the globe. In many instances, these pathways are broadly reproduced geographically in different chemical-transport models. The models, however, have difficulties at times with accurately projecting the vertical distribution of aerosols, which can lead to significant discrepancies in the lifetimes of the modeled aerosols. This issue is compounded at high latitudes where observations are especially sparse. New measurements from the CALIPSO satellite mission can provide additional insight on the vertical distribution of aerosols over the globe. The mission is a joint effort between the United States (NASA) and France (CNES) and was launched on April 28, 2008 into the A-train satellite constellation. CALIPSO's primary instrument is a two-wavelength polarization-sensitive lidar operating at 532 and 1064 nm with a repetition rate of 20.16 Hz. Lidar observations in the lower troposphere (¡ 8 km) have a vertical resolution of 30 m for the 532 nm channel and 60 m for the 1064 channel. The instrument has been operational since early June 2006. The CALIPSO data set reveals a rich distribution of aerosols in clear and cloudy scenes for both day and night conditions. Information on aerosol type is also available based on their wavelength dependence and polarization characteristics. From these data, a climatology on the vertical and geographic distribution and optical characteristics of aerosols (and clouds) is being developed that can aid diagnostic studies of aerosol transport

  6. CCN frequency distributions and aerosol chemical composition from long-term observations at European ACTRIS supersites

    NASA Astrophysics Data System (ADS)

    Decesari, Stefano; Rinaldi, Matteo; Schmale, Julia Yvonne; Gysel, Martin; Fröhlich, Roman; Poulain, Laurent; Henning, Silvia; Stratmann, Frank; Facchini, Maria Cristina

    2016-04-01

    Cloud droplet number concentration is regulated by the availability of aerosol acting as cloud condensation nuclei (CCN). Predicting the air concentrations of CCN involves knowledge of all physical and chemical processes that contribute to shape the particle size distribution and determine aerosol hygroscopicity. The relevance of specific atmospheric processes (e.g., nucleation, coagulation, condensation of secondary organic and inorganic aerosol, etc.) is time- and site-dependent, therefore the availability of long-term, time-resolved aerosol observations at locations representative of diverse environments is strategic for the validation of state-of-the-art chemical transport models suited to predict CCN concentrations. We focused on long-term (year-long) datasets of CCN and of aerosol composition data including black carbon, and inorganic as well as organic compounds from the Aerosol Chemical Speciation Monitor (ACSM) at selected ACTRIS supersites (http://www.actris.eu/). We discuss here the joint frequency distribution of CCN levels and of aerosol chemical components concentrations for two stations: an alpine site (Jungfraujoch, CH) and a central European rural site (Melpitz, DE). The CCN frequency distributions at Jungfraujoch are broad and generally correlated with the distributions of the concentrations of aerosol chemical components (e.g., high CCN concentrations are most frequently found for high organic matter or black carbon concentrations, and vice versa), which can be explained as an effect of the strong seasonality in the aerosol characteristics at the mountain site. The CCN frequency distributions in Melpitz show a much weaker overlap with the distributions of BC concentrations or other chemical compounds. However, especially at high CCN concentration levels, a statistical correlation with organic matter (OM) concentration can be observed. For instance, the number of CCN (with particle diameter between 20 and 250 nm) at a supersaturation of 0.7% is

  7. Assessment of the Aerosol Distribution Over Indian Subcontinent in CMIP5 Models

    NASA Astrophysics Data System (ADS)

    Sanap, S. D.; Pandithurai, G.

    2014-12-01

    This paper examines the aerosol distribution over Indian subcontinent as represented in 21 models from Coupled Model Inter-comparison Project Phase 5 (CMIP5) simulations, wherein model simulated aerosol optical depth (AOD) is compared with Moderate Resolution Imaging Spectro-radiometer (MODIS) satellite observations. The objective of the study is to provide an assessment of the capability of various global models, participating in CMIP5 project, in capturing the realistic spatial and temporal distribution of aerosol species over the Indian subcontinent. Results from our analysis show that majority of the CMIP5 models seriously underestimates the spatio-temporal variability of aerosol species over the Indian subcontinent, in particular over Indo-Gangetic Plains(IGP). Though the representation of black carbon (BC) loading in many models is fairly good, the dust loading is observed to be significantly low in majority of the models. The presence of pronounced dust activity over northern India and dust being one of the major constituent of aerosol species, the biases in dust loading has a great impact on the AOD of that region. We found that considerable biases in simulating the 850 hPa wind field (which plays important role in transport of dust from adjacent deserts) would be the possible reason for poor representation of dust AOD and in turn total AOD over Indian region in CMIP5 models. In addition, aerosol radiative forcing (ARF) underestimated/overestimated in most of the models. However, spatial distribution of ARF in multi-model ensemble mean is comparable reasonably well with observations with bias in magnitudes. This analysis emphasizes the fundamental need to improve the representation of aerosol species in current state of the art climate models. As reported in Intergovernmental Panel on Climate Change (IPCC) fourth assessment report (AR4), the level of scientific understanding (LOSU) of climatic impact of aerosols is medium-low. For better understanding of

  8. A-Train satellite measurements of dust aerosol distributions over northern China

    NASA Astrophysics Data System (ADS)

    Wang, Hongbin; Zhang, Lei; Cao, Xianjie; Zhang, Zhiwei; Liang, Jiening

    2013-06-01

    Horizontal and vertical distributions of dust aerosols over northern China were investigated for the period June 2006 to May 2011 using A-Train satellite constellation data and ground-based measurements. Surface observations at 675 meteorological stations showed that dust events occurred most frequently in the Taklamakan and Gobi deserts. In the Taklamakan Desert, the dust aerosol content was high throughout the year, as seen from the distributions of the Moderate-Resolution Imaging Spectroradiometer (MODIS) aerosol optical depth (AOD) and the Ozone Monitoring Instrument (OMI) UV-absorption aerosol index (AAI). In the Taklamakan and Gobi deserts, the AOD and AAI reached maxima in spring and minima in winter. In the eastern part of northern China, AOD reached a maximum in summer and a minimum in fall, whereas AAI was high in winter and spring and low in summer and fall due to seasonal differences in the main aerosol type. The dust observations revealed strong seasonal variations in dust coverage area and height, with maxima in spring and summer and minima in fall and winter. The transportation of dust aerosols in all seasons was confined largely between 35°N and 45°N. The mean height of the dust layer top varied and showed strong seasonal variation in all regions, with values higher than 4km in spring and about 2km in winter. The Taklamakan Desert experienced higher occurrence of dust events than other regions throughout the year. Dust occurrence decreased dramatically over the eastern part of northern China in summer because of surface vegetation and precipitation. Simulation results by the HYSPLIT model were similar to the distribution of dust aerosols observed by the Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP) during the same period.

  9. Quantifying the climatological cloud-free shortwave direct radiative forcing of mineral dust aerosol over the Red Sea

    NASA Astrophysics Data System (ADS)

    Stenchikov, G. L.; Brindley, H. E.; Osipov, S.; Bantges, R. J.; Smirnov, A.; Prakash, P. J.

    2014-12-01

    While there have been a number of campaigns designed to probe dust-climate interactions over much of the world, relatively little attention has been paid to the Red Sea. Because of the remoteness of the area, satellite retrievals provide a crucial tool for assessing aerosol loading over the Sea. However, agreement between aerosol properties inferred from measurements from different instruments, and even in some cases from the same measurements using different retrieval algorithms can be poor, particularly in the case of mineral dust. Ground based measurements, which can be used to evaluate retrievals, are thus highly desirable. Here we take advantage of ship-based hand-held sun-photometer (microtops) observations gathered within the framework of NASA Aerosol Maritime Network from a series of cruises, which took place across the Red Sea during 2011 and 2013. To our knowledge these data represent the first set of detailed aerosol measurements from the Sea. They thus provide a unique opportunity to assess the performance of satellite retrieval algorithms in this region. Here we used the microtops measurements to evaluate the performance of co-located satellite retrievals from the Spinning Enhanced Visible and InfraRed Imager (SEVIRI) and the MODerate Imaging Spectrometer (MODIS). Both algorithms show good agreement with the ship-based measurements and with each other, although it appears that the MODIS cloud detection scheme in particular is rather conservative. The stand alone Rapid Radiative Transfer Model (RRTM) driven by reanalysis meteorological fields is used to estimate the cloud-free aerosol direct radiative effect at the surface and TOA along the ship tracks. The TOA effects are compared to co-located measurements from the Geostationary Earth Radiation Budget (GERB) instrument. Having evaluated both the quality of the retrievals and the ability of the model to capture the associated radiative effect, we will present a climatology of aerosol loading over the

  10. Dissolved organic matter in sea spray: a transfer study from marine surface water to aerosols

    NASA Astrophysics Data System (ADS)

    Schmitt-Kopplin, P.; Liger-Belair, G.; Koch, B. P.; Flerus, R.; Kattner, G.; Harir, M.; Kanawati, B.; Lucio, M.; Tziotis, D.; Hertkorn, N.; Gebefügi, I.

    2011-12-01

    Atmospheric aerosols impose direct and indirect effects on the climate system, for example, by adsorption of radiation in relation to cloud droplets size, on chemical and organic composition and cloud dynamics. The first step in the formation of primary marine aerosols, i.e., the transfer of dissolved organic matter from the marine surface into the atmosphere was studied, and we present a molecular level description of this phenomenon using high resolution analytical tools (Fourier transform ion cyclotron resonance = FT-ICR MS and NMR). We could experimentally confirm the chemo-selective transfer of natural organic molecules, especially of aliphatic compounds from the surface water into the atmosphere via bubble bursting processes. Transfer from marine surface water to the atmosphere involves a chemical gradient governed by the physicochemical properties of the involved molecules when comparing elemental compositions and differentiating CHO, CHNO, CHOS and CHNOS bearing compounds. Typical chemical fingerprints of concentrated compounds were CHO and CHOS type of molecules, smaller molecules of higher aliphaticity and lower oxygen content and typical surfactants. A non-targeted mass spectrometric analysis of the samples showed that many of these molecules correspond to homologous series of oxo-, hydroxyl-, methoxy-, branched fatty acids and mono-, di- and tricarboxylic acids as well as monoterpenes and sugars. These surface active biomolecules were preferentially transferred from surface water into the atmosphere via bubble bursting processes to form a significant fraction of primary organic aerosols. This way of production of sea spray leaves a specific biological signature of the surface water in the corresponding lower atmosphere that can be transported laterally in the context of global cycling.

  11. From BASE-ASIA Toward 7-SEAS: A Satellite-Surface Perspective of Boreal Spring Biomass-Burning Aerosols and Clouds in Southeast Asia

    NASA Technical Reports Server (NTRS)

    Tsay, Si-Chee; Hsu, N. Christina; Lau, William K.-M.; Li, Can; Gabriel, Philip M.; Ji, Qiang; Holben, Brent N.; Welton, E. Judd; Nguyen, Anh X.; Janjai, Serm; Lin, Neng-Huei; Reid, Jeffrey S.; Boonjawat, Jariya; Howell, Steven G.; Huebert, Barry J.; Fu, Joshua S.; Hansell, Richard A.; Sayer, Andrew M.; Gautam, Ritesh; Wang, Sheng-Hsiang; Goodloe, Colby S.; Miko, Laddawan R.; Shu, Peter K.; Loftus, Adrian M.; Huang, Jingfeng; Kim, Jin Young; Jeong, Myeong-Jae; Pantina, Peter

    2013-01-01

    In this paper, we present recent field studies conducted by NASA's SMART-COMMIT (and ACHIEVE, to be operated in 2013) mobile laboratories, jointly with distributed ground-based networks (e.g., AERONET, http://aeronet.gsfc.nasa.gov/ and MPLNET, http://mplnet.gsfc.nasa.gov/) and other contributing instruments over northern Southeast Asia. These three mobile laboratories, collectively called SMARTLabs (cf. http://smartlabs.gsfc.nasa.gov/, Surface-based Mobile Atmospheric Research & Testbed Laboratories) comprise a suite of surface remote sensing and in-situ instruments that are pivotal in providing high spectral and temporal measurements, complementing the collocated spatial observations from various Earth Observing System (EOS) satellites. A satellite-surface perspective and scientific findings, drawn from the BASE-ASIA (2006) field deployment as well as a series of ongoing 7-SEAS (2010-13) field activities over northern Southeast Asia are summarized, concerning (i) regional properties of aerosols from satellite and in situ measurements, (ii) cloud properties from remote sensing and surface observations, (iii) vertical distribution of aerosols and clouds, and (iv) regional aerosol radiative effects and impact assessment. The aerosol burden over Southeast Asia in boreal spring, attributed to biomass burning, exhibits highly consistent spatial and temporal distribution patterns, with major variability arising from changes in the magnitude of the aerosol loading mediated by processes ranging from large-scale climate factors to diurnal meteorological events. Downwind from the source regions, the tightly coupled-aerosolecloud system provides a unique, natural laboratory for further exploring the micro- and macro-scale relationships of the complex interactions. The climatic significance is presented through large-scale anti-correlations between aerosol and precipitation anomalies, showing spatial and seasonal variability, but their precise cause-and-effect relationships

  12. Sea spray aerosol as a unique source of ice nucleating particles

    NASA Astrophysics Data System (ADS)

    DeMott, Paul J.; Hill, Thomas C. J.; McCluskey, Christina S.; Prather, Kimberly A.; Collins, Douglas B.; Sullivan, Ryan C.; Ruppel, Matthew J.; Mason, Ryan H.; Irish, Victoria E.; Lee, Taehyoung; Hwang, Chung Yeon; Siek Rhee, Tae; Snider, Jefferson R.; McMeeking, Gavin R.; Dhaniyala, Suresh; Lewis, Ernie R.; Wentzell, Jeremy J. B.; Abbatt, Jonathan; Lee, Christopher; Sultana, Camille M.; Ault, Andrew P.; Axson, Jessica L.; Diaz Martinez, Myrelis; Venero, Ingrid; Santos-Figueroa, Gilmarie; Stokes, M. Dale; Deane, Grant B.; Mayol-Bracero, Olga L.; Grassian, Vicki H.; Bertram, Timothy H.; Bertram, Allan K.; Moffett, Bruce F.; Franc, Gary D.

    2016-05-01

    Ice nucleating particles (INPs) are vital for ice initiation in, and precipitation from, mixed-phase clouds. A source of INPs from oceans within sea spray aerosol (SSA) emissions has been suggested in previous studies but remained unconfirmed. Here, we show that INPs are emitted using real wave breaking in a laboratory flume to produce SSA. The number concentrations of INPs from laboratory-generated SSA, when normalized to typical total aerosol number concentrations in the marine boundary layer, agree well with measurements from diverse regions over the oceans. Data in the present study are also in accord with previously published INP measurements made over remote ocean regions. INP number concentrations active within liquid water droplets increase exponentially in number with a decrease in temperature below 0 °C, averaging an order of magnitude increase per 5 °C interval. The plausibility of a strong increase in SSA INP emissions in association with phytoplankton blooms is also shown in laboratory simulations. Nevertheless, INP number concentrations, or active site densities approximated using “dry” geometric SSA surface areas, are a few orders of magnitude lower than corresponding concentrations or site densities in the surface boundary layer over continental regions. These findings have important implications for cloud radiative forcing and precipitation within low-level and midlevel marine clouds unaffected by continental INP sources, such as may occur over the Southern Ocean.

  13. Sea spray aerosol as a unique source of ice nucleating particles.

    PubMed

    DeMott, Paul J; Hill, Thomas C J; McCluskey, Christina S; Prather, Kimberly A; Collins, Douglas B; Sullivan, Ryan C; Ruppel, Matthew J; Mason, Ryan H; Irish, Victoria E; Lee, Taehyoung; Hwang, Chung Yeon; Rhee, Tae Siek; Snider, Jefferson R; McMeeking, Gavin R; Dhaniyala, Suresh; Lewis, Ernie R; Wentzell, Jeremy J B; Abbatt, Jonathan; Lee, Christopher; Sultana, Camille M; Ault, Andrew P; Axson, Jessica L; Diaz Martinez, Myrelis; Venero, Ingrid; Santos-Figueroa, Gilmarie; Stokes, M Dale; Deane, Grant B; Mayol-Bracero, Olga L; Grassian, Vicki H; Bertram, Timothy H; Bertram, Allan K; Moffett, Bruce F; Franc, Gary D

    2016-05-24

    Ice nucleating particles (INPs) are vital for ice initiation in, and precipitation from, mixed-phase clouds. A source of INPs from oceans within sea spray aerosol (SSA) emissions has been suggested in previous studies but remained unconfirmed. Here, we show that INPs are emitted using real wave breaking in a laboratory flume to produce SSA. The number concentrations of INPs from laboratory-generated SSA, when normalized to typical total aerosol number concentrations in the marine boundary layer, agree well with measurements from diverse regions over the oceans. Data in the present study are also in accord with previously published INP measurements made over remote ocean regions. INP number concentrations active within liquid water droplets increase exponentially in number with a decrease in temperature below 0 °C, averaging an order of magnitude increase per 5 °C interval. The plausibility of a strong increase in SSA INP emissions in association with phytoplankton blooms is also shown in laboratory simulations. Nevertheless, INP number concentrations, or active site densities approximated using "dry" geometric SSA surface areas, are a few orders of magnitude lower than corresponding concentrations or site densities in the surface boundary layer over continental regions. These findings have important implications for cloud radiative forcing and precipitation within low-level and midlevel marine clouds unaffected by continental INP sources, such as may occur over the Southern Ocean. PMID:26699469

  14. Sea spray aerosol as a unique source of ice nucleating particles

    PubMed Central

    DeMott, Paul J.; Hill, Thomas C. J.; McCluskey, Christina S.; Prather, Kimberly A.; Ruppel, Matthew J.; Mason, Ryan H.; Irish, Victoria E.; Lee, Taehyoung; Hwang, Chung Yeon; Snider, Jefferson R.; McMeeking, Gavin R.; Dhaniyala, Suresh; Lewis, Ernie R.; Wentzell, Jeremy J. B.; Abbatt, Jonathan; Lee, Christopher; Sultana, Camille M.; Ault, Andrew P.; Axson, Jessica L.; Diaz Martinez, Myrelis; Venero, Ingrid; Santos-Figueroa, Gilmarie; Stokes, M. Dale; Deane, Grant B.; Mayol-Bracero, Olga L.; Grassian, Vicki H.; Bertram, Timothy H.; Bertram, Allan K.; Moffett, Bruce F.; Franc, Gary D.

    2016-01-01

    Ice nucleating particles (INPs) are vital for ice initiation in, and precipitation from, mixed-phase clouds. A source of INPs from oceans within sea spray aerosol (SSA) emissions has been suggested in previous studies but remained unconfirmed. Here, we show that INPs are emitted using real wave breaking in a laboratory flume to produce SSA. The number concentrations of INPs from laboratory-generated SSA, when normalized to typical total aerosol number concentrations in the marine boundary layer, agree well with measurements from diverse regions over the oceans. Data in the present study are also in accord with previously published INP measurements made over remote ocean regions. INP number concentrations active within liquid water droplets increase exponentially in number with a decrease in temperature below 0 °C, averaging an order of magnitude increase per 5 °C interval. The plausibility of a strong increase in SSA INP emissions in association with phytoplankton blooms is also shown in laboratory simulations. Nevertheless, INP number concentrations, or active site densities approximated using “dry” geometric SSA surface areas, are a few orders of magnitude lower than corresponding concentrations or site densities in the surface boundary layer over continental regions. These findings have important implications for cloud radiative forcing and precipitation within low-level and midlevel marine clouds unaffected by continental INP sources, such as may occur over the Southern Ocean. PMID:26699469

  15. Sea spray aerosol as a unique source of ice nucleating particles.

    PubMed

    DeMott, Paul J; Hill, Thomas C J; McCluskey, Christina S; Prather, Kimberly A; Collins, Douglas B; Sullivan, Ryan C; Ruppel, Matthew J; Mason, Ryan H; Irish, Victoria E; Lee, Taehyoung; Hwang, Chung Yeon; Rhee, Tae Siek; Snider, Jefferson R; McMeeking, Gavin R; Dhaniyala, Suresh; Lewis, Ernie R; Wentzell, Jeremy J B; Abbatt, Jonathan; Lee, Christopher; Sultana, Camille M; Ault, Andrew P; Axson, Jessica L; Diaz Martinez, Myrelis; Venero, Ingrid; Santos-Figueroa, Gilmarie; Stokes, M Dale; Deane, Grant B; Mayol-Bracero, Olga L; Grassian, Vicki H; Bertram, Timothy H; Bertram, Allan K; Moffett, Bruce F; Franc, Gary D

    2016-05-24

    Ice nucleating particles (INPs) are vital for ice initiation in, and precipitation from, mixed-phase clouds. A source of INPs from oceans within sea spray aerosol (SSA) emissions has been suggested in previous studies but remained unconfirmed. Here, we show that INPs are emitted using real wave breaking in a laboratory flume to produce SSA. The number concentrations of INPs from laboratory-generated SSA, when normalized to typical total aerosol number concentrations in the marine boundary layer, agree well with measurements from diverse regions over the oceans. Data in the present study are also in accord with previously published INP measurements made over remote ocean regions. INP number concentrations active within liquid water droplets increase exponentially in number with a decrease in temperature below 0 °C, averaging an order of magnitude increase per 5 °C interval. The plausibility of a strong increase in SSA INP emissions in association with phytoplankton blooms is also shown in laboratory simulations. Nevertheless, INP number concentrations, or active site densities approximated using "dry" geometric SSA surface areas, are a few orders of magnitude lower than corresponding concentrations or site densities in the surface boundary layer over continental regions. These findings have important implications for cloud radiative forcing and precipitation within low-level and midlevel marine clouds unaffected by continental INP sources, such as may occur over the Southern Ocean.

  16. Aliphatic and aromatic hydrocarbons in different sized aerosols over the Mediterranean Sea: Occurrence and origin

    NASA Astrophysics Data System (ADS)

    Sicre, M. A.; Marty, J. C.; Saliot, A.; Aparicio, X.; Grimalt, J.; Albaiges, J.

    Marine aerosols were collected using a five-stage cascade impactor during the PHYCEMED II cruise in the Western Mediterranean Sea (October 1983). Their composition in aliphatic and aromatic hydrocarbons (HCs) was analyzed, representing the first time that concentrations of polynuclear aromatic HCs (PAH) are reported in relation to particle size for aerosols of remote marine areas. The HC concentrations were found to be dependent on the origin of the air masses. They were higher for air coming from North European countries than for air originating in the Atlantic and the South of Spain. The concentrations range between 7 and 14 ng m -3for n-alkanes and between 0.2 and 0.4 ng m -3for total PAH. Based on molecular criteria, several sources for these HCs have been identified: continental higher plant waxes, petroleum and pyrolysis (namely coal combustion and vehicular exhausts). Mass medium equivalent diameters (MMED) for the naturally derived n-alkanes are in the 1.79-2.53 μm range, indicating an origin related with the emission of large particles from higher plant waxes or from soil dusts. In contrast, MMED for the anthropogenic HCs, both aliphatic and aromatic, are smaller than the micron, suggesting initial emission of PAH through pyrolytic processes in the vapor phase followed by condensation onto larger sub-μm particles.

  17. 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.

  18. Aerosol size distribution characteristics of organosulfates in the Pearl River Delta region, China

    NASA Astrophysics Data System (ADS)

    Kuang, Bin Yu; Lin, Peng; Hu, Min; Yu, Jian Zhen

    2016-04-01

    Organosulfates (OSs) have been detected in various atmospheric environments, but their particle size distribution characteristics are unknown. In this work, we examined their size distributions in ambient aerosols to gain insights into the formation processes. Size-segregated aerosol samples in the range of 0.056-18 μm were collected using a ten-stage impactor at a receptor site in Hong Kong in both summer and winter and in Nansha in the Pearl River Delta in winter. The humic-like substances fraction in the size-segregated samples was isolated and analyzed using electrospray ionization coupled with an Orbitrap Ultra High Resolution Mass Spectrometer. Through accurate mass measurements, ∼190 CHOS and ∼90 CHONS formulas were tentatively identified to be OS compounds. Among them, OS compounds derived from isoprene, α-/β-pinene, and limonene and alkyl OSs having low double bond equivalents (DBE = 0,1) and 0-2 extra O beyond those in -OSO3 were found with high intensity. The biogenic volatile organic compounds-derived OS formulas share a common characteristic with sulfate in that the droplet mode dominated, peaking in either 0.56-1.0 or 1.0-1.8 μm size bin, reflecting sulfate as their common precursor. Most of these OSs have a minor coarse mode, accounting for 0-45%. The presence of OSs on the coarse particles is hypothesized to be a result of OSs on small particle (<0.32 μm) coagulating with coarse particles, as the abundance ratios of OS to non-sea-salt sulfate present on the coarse particles were similar to those on particles <0.32 μm. Among a few pairs of CHONS and CHOS that could be linked up through hydrolysis of a nitrooxy group in the CHONS form (e.g., m/z 294: C10H16O7NS- vs. m/z 249 C10H17O5S- from α/β-pinene, differing by (+H2O-HNO3)), the CHONS compounds had an enhanced coarse mode presence. This could be interpreted as a result of slower hydrolysis of the CHONS compounds on the alkali coarse particles. The low DBE alkyl OS compounds have a

  19. Iterative method for the inversion of multiwavelength lidar signals to determine aerosol size distribution.

    PubMed

    Rajeev, K; Parameswaran, K

    1998-07-20

    Two iterative methods of inverting lidar backscatter signals to determine altitude profiles of aerosol extinction and altitude-resolved aerosol size distribution (ASD) are presented. The first method is for inverting two-wavelength lidar signals in which the shape of the ASD is assumed to be of power-law type, and the second method is for inverting multiwavelength lidar signals without assuming any a priori analytical form of ASD. An arbitrary value of the aerosol extinction-to-backscatter ratio (S(1)) is assumed initially to invert the lidar signals, and the ASD determined by use of the spectral dependence of the retrieved aerosol extinction coefficients is used to improve the value of S(1) iteratively. The methods are tested for different forms of altitude-dependent ASD's by use of simulated lidar-backscatter-signal profiles. The effect of random noise on the lidar backscatter signals is also studied.

  20. Aerosol vertical distribution, optical properties and transport over Corsica (western Mediterranean)

    NASA Astrophysics Data System (ADS)

    Léon, J.-F.; Augustin, P.; Mallet, M.; Bourrianne, T.; Pont, V.; Dulac, F.; Fourmentin, M.; Lambert, D.; Sauvage, B.

    2015-03-01

    This paper presents the aerosol vertical distribution observed in the western Mediterranean between February and April 2011 and between February 2012 and August 2013. An elastic backscattering lidar was continuously operated at a coastal site in the northern part of Corsica Island (Cap Corse) for a total of more than 14 000 h of observations. The aerosol extinction coefficient retrieved from cloud-free lidar profiles are analyzed along with the SEVIRI satellite aerosol optical depth (AOD). The SEVIRI AOD was used to constrain the retrieval of the aerosol extinction profiles from the lidar range-corrected signal and to detect the presence of dust or pollution aerosols. The daily average AOD at 550 nm is 0.16 (±0.09) and ranges between 0.05 and 0.80. A seasonal cycle is observed with minima in winter and maxima in spring-summer. High AOD days (above 0.3 at 550 nm) represent less than 10% of the totality of daily observations and correspond to the large scale advection of desert dust from Northern Africa or pollution aerosols from Europe. The respective origin of the air masses is confirmed using FLEXPART simulations in the backward mode. Dust events are characterized by a large turbid layer between 2 and 5 km height while pollution events show a lower vertical development with a thick layer below 3 km in altitude. However low level dust transport is also reported during spring while aerosol pollution layer between 2 and 4 km height has been also observed. We report an effective lidar ratio at 355 nm for pollution aerosols 68 (±13) Sr while it is 63 (±18) Sr for dust. The daily mean AOD at 355 nm for dust events is 0.61 (±0.14) and 0.71 (±0.16) for pollution aerosols events.

  1. Marine biogeochemical influence on primary sea spray aerosol composition in the Southern Ocean: predictions from a mechanistic model

    NASA Astrophysics Data System (ADS)

    McCoy, D.; Burrows, S. M.; Elliott, S.; Frossard, A. A.; Russell, L. M.; Liu, X.; Ogunro, O. O.; Easter, R. C.; Rasch, P. J.

    2014-12-01

    Remote marine clouds, such as those over the Southern Ocean, are particularly sensitive to variations in the concentration and chemical composition of aerosols that serve as cloud condensation nuclei (CCN). Observational evidence indicates that the organic content of fine marine aerosol is greatly increased during the biologically active season near strong phytoplankton blooms in certain locations, while being nearly constant in other locations. We have recently developed a novel modeling framework that mechanistically links the organic fraction of submicron sea spray to ocean biogeochemistry (Burrows et al., in discussion, ACPD, 2014; Elliott et al., ERL, 2014). Because of its combination of large phytoplankton blooms and high wind speeds, the Southern Ocean is an ideal location for testing our understanding of the processes driving the enrichment of organics in sea spray aerosol. Comparison of the simulated OM fraction with satellite observations shows that OM fraction is a statistically significant predictor of cloud droplet number concentration over the Southern Ocean. This presentation will focus on predictions from our modeling framework for the Southern Ocean, specifically, the predicted geographic gradients and seasonal cycles in the aerosol organic matter and its functional group composition. The timing and location of a Southern Ocean field campaign will determine its utility in observing the effects of highly localized and seasonal phytoplankton blooms on aerosol composition and clouds. Reference cited: Burrows, S. M., Ogunro, O., Frossard, A. A., Russell, L. M., Rasch, P. J., and Elliott, S.: A physically-based framework for modelling the organic fractionation of sea spray aerosol from bubble film Langmuir equilibria, Atmos. Chem. Phys. Discuss., 14, 5375-5443, doi:10.5194/acpd-14-5375-2014, 2014. Elliott, S., Burrows, S. M., Deal, C., Liu, X., Long, M., Ogunro, O., Russell, L. M., and Wingenter O.. "Prospects for simulating macromolecular surfactant

  2. The Influence of Tropical Air-Sea Interaction on the Climate Impact of Aerosols: A Hierarchical Modeling Approach

    NASA Astrophysics Data System (ADS)

    Hsieh, W. C.; Saravanan, R.; Chang, P.; Mahajan, S.

    2014-12-01

    In this study, we use a hierarchical modeling approach to investigate the influence of tropical air-sea feedbacks on climate impacts of aerosols in the Community Earth System Model (CESM). We construct four different models by coupling the atmospheric component of CESM, the Community Atmospheric Model (CAM), to four different ocean models: (i) the Data Ocean Model (DOM; prescribed SST), (i) Slab Ocean Model (SOM; thermodynamic coupling), (iii) Reduced Gravity Ocean Model (RGOM; dynamic coupling), and (iv) the Parallel Ocean Program (POP; full ocean model). These four models represent progressively increasing degree of coupling between the atmosphere and the ocean. The RGOM model, in particular, is tuned to produce a good simulation of ENSO and the associated tropical air-sea interaction, without being impacted by the climate drifts exhibited by fully-coupled GCMs. For each method of coupling, a pair of numerical experiments, including present day (year 2000) and preindustrial (year 1850) sulfate aerosol loading, were carried out. Our results indicate that the inclusion of air-sea interaction has large impacts on the spatial structure of the climate response induced by aerosols. In response to sulfate aerosol forcing, ITCZ shifts southwards as a result of the anomalous clockwise MMC change which transports moisture southwardly across the Equator. We present analyses of the regional response to sulfate aerosol forcing in the equatorial Pacific as well as the zonally-averaged response. The decomposition of the change in the net surface energy flux shows the most dominant terms are net shortwave radiative flux at the surface and latent heat flux. Further analyses show all ocean model simulations simulate a positive change of northward atmospheric energy transport across the Equator in response to the perturbed radiative sulfate forcing. This positive northward atmospheric energy transport change plays a role in compensating partially cooling caused by sulfate aerosols.

  3. Sea quark transverse momentum distributions and dynamical chiral symmetry breaking

    SciTech Connect

    Schweitzer, Peter; Strikman, Mark; Weiss, Christian

    2014-01-01

    Recent theoretical studies have provided new insight into the intrinsic transverse momentum distributions of valence and sea quarks in the nucleon at a low scale. The valence quark transverse momentum distributions (q - qbar) are governed by the nucleon's inverse hadronic size R{sup -1} ~ 0.2 GeV and drop steeply at large p{sub T}. The sea quark distributions (qbar) are in large part generated by non-perturbative chiral-symmetry breaking interactions and extend up to the scale rho{sup -1} ~ 0.6 GeV. These findings have many implications for modeling the initial conditions of perturbative QCD evolution of TMD distributions (starting scale, shape of p{sub T}. distributions, coordinate-space correlation functions). The qualitative difference between valence and sea quark intrinsic p{sub T}. distributions could be observed experimentally, by comparing the transverse momentum distributions of selected hadrons in semi-inclusive deep-inelastic scattering, or those of dileptons produced in pp and pbar-p scattering.

  4. Physicochemical characterization of Capstone depleted uranium aerosols II: particle size distributions as a function of time.

    PubMed

    Cheng, Yung Sung; Kenoyer, Judson L; Guilmette, Raymond A; Parkhurst, Mary Ann

    2009-03-01

    The Capstone Depleted Uranium (DU) Aerosol Study, which generated and characterized aerosols containing DU from perforation of armored vehicles with large-caliber DU penetrators, incorporated a sampling protocol to evaluate particle size distributions. Aerosol particle size distribution is an important parameter that influences aerosol transport and deposition processes as well as the dosimetry of the inhaled particles. These aerosols were collected on cascade impactor substrates using a pre-established time sequence following the firing event to analyze the uranium concentration and particle size of the aerosols as a function of time. The impactor substrates were analyzed using proportional counting, and the derived uranium content of each served as input to the evaluation of particle size distributions. Activity median aerodynamic diameters (AMADs) of the particle size distributions were evaluated using unimodal and bimodal models. The particle size data from the impactor measurements were quite variable. Most size distributions measured in the test based on activity had bimodal size distributions with a small particle size mode in the range of between 0.2 and 1.2 microm and a large size mode between 2 and 15 microm. In general, the evolution of particle size over time showed an overall decrease of average particle size from AMADs of 5 to 10 microm shortly after perforation to around 1 microm at the end of the 2-h sampling period. The AMADs generally decreased over time because of settling. Additionally, the median diameter of the larger size mode decreased with time. These results were used to estimate the dosimetry of inhaled DU particles. PMID:19204485

  5. CLOUDS, AEROSOLS, RADIATION AND THE AIR-SEA INTERFACE OF THE SOUTHERN OCEAN: ESTABLISHING DIRECTIONS FOR FUTURE RESEARCH

    SciTech Connect

    Wood, Robert; Bretherton, Chris; McFarquhar, Greg; Protat, Alain; Quinn, Patricia; Siems, Steven; Jakob, Christian; Alexander, Simon; Weller, Bob

    2014-09-29

    A workshop sponsored by the Department of Energy was convened at the University of Washington to discuss the state of knowledge of clouds, aerosols and air-sea interaction over the Southern Ocean and to identify strategies for reducing uncertainties in their representation in global and regional models. The Southern Ocean plays a critical role in the global climate system and is a unique pristine environment, yet other than from satellite, there have been sparse observations of clouds, aerosols, radiation and the air-sea interface in this region. Consequently, much is unknown about atmospheric and oceanographic processes and their linkage in this region. Approximately 60 scientists, including graduate students, postdoctoral fellows and senior researchers working in atmospheric and oceanic sciences at U.S. and foreign universities and government laboratories, attended the Southern Ocean Workshop. It began with a day of scientific talks, partly in plenary and partly in two parallel sessions, discussing the current state of the science for clouds, aerosols and air-sea interaction in the Southern Ocean. After the talks, attendees broke into two working groups; one focused on clouds and meteorology, and one focused on aerosols and their interactions with clouds. This was followed by more plenary discussion to synthesize the two working group discussions and to consider possible plans for organized activities to study clouds, aerosols and the air-sea interface in the Southern Ocean. The agenda and talk slides, including short summaries of the highlights of the parallel session talks developed by the session chars, are available at http://www.atmos.washington.edu/socrates/presentations/SouthernOceanPresentations/.

  6. 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.

  7. [Nutrient distributions and their limitation on phytoplankton in the Yellow Sea and the East China Sea].

    PubMed

    Wang, Baodong

    2003-07-01

    Based on field observations during 1997 to 1999, the distributions of micronutrients and their limitation on the growth of phytoplankton in the Yellow Sea and the East China Sea were discussed in this paper. The results showed that there were abundant nutrients in the area of the east and northern-east of the Changjiang River estuary, and the nutrients came from the extension of the Changjiang River diluted water and the transportation of the Subei Coastal water. Besides, the maximum extension range of the nutrients in the Changjiang River diluted water was observed during the catastrophic flooding period of the Changjiang River in the summer of 1998. Based on the Redfield ratio (Si:N:P = 16:16:1) in which, three essential nutrients were utilized by marine phytoplankton, the Si/N/P ratios were calculated and studied for the upper water of the Yellow Sea and the East China Sea. The results indicated that Si/N ratios were very high, which suggested that silicate was not the limiting factor for the growth of phytoplankton in the Yellow Sea and the East China Sea. However, under the influence of terrestrial runoff, especially the Changjiang River runoff which was rich in combined nitrogen and had very high N/P ratios, high N/P ratios occurred in the Changjiang River estuary and its adjacent areas such as the south and southwest of the Yellow Sea, the inshore area of the East China Sea and the area east of the Changjiang River estuary in spring and summer. As a result, in contrast to general open marine systems, the systems in these areas resembled estuarine ones rather than typical marine ones. The primary production in a considerable portion of the Yellow Sea and the East China Sea might be limited by phosphate rather than nitrogen.

  8. Chemical Composition and Size Distributions of Coastal Aerosols Observed on the U.S. East Coast

    NASA Astrophysics Data System (ADS)

    Xia, L.; Song, F.; Jusino-Atresino, R.; Thuman, C.; Gao, Y.

    2008-12-01

    Aerosol input is an important source of certain limiting nutrients, such as iron, for phytoplankton growth in several large oceanic regions. As the efficiency of biological uptake of nutrients may depend on the aerosol properties, a better knowledge of aerosol properties is critically important. Characterizing aerosols over the coastal ocean needs special attention, because the properties of aerosols could be altered by many anthropogenic processes in this land-ocean transition zone before they are transported over the remote ocean. The goal of this experiment was to examine aerosol properties, in particular chemical composition, particle-size distributions and iron solubility, over the US Eastern Seaboard, an important boundary for the transport of continental substances from North America to the North Atlantic Ocean. Our field sampling site was located at Tuckerton (39°N, 74°W) on the southern New Jersey coast. Fourteen sets of High-Volume aerosol samples and three sets of size segregated aerosol samples by a 10-stage MOUDI impactor were collected during 2007 and 2008. The ICP-MS methodology was used to analyze aerosol samples for the concentrations of thirteen trace elements: Al, Fe, Mn, Sc, Cd, Pb, Sb, Ni, Co, Cr, Cu, Zn and V. The IC procedures were applied to determine five cations (sodium, ammonium, potassium, magnesium and calcium) and eleven anions (fluoride, acetate, propionate, formate, MSA, chloride, nitrate, succinate, malonate, sulfate and oxalate). The UV spectrometry was employed for the determination of iron solubility. Preliminary results suggest three major sources of aerosols: anthropogenic, crustal and marine. At this location, the concentrations of iron (II) ranged from 2.8 to 29ng m-3, accounting for ~20% of the total iron. The iron concentrations at this coastal site were substantially lower than those observed in Newark, an urban site in northern NJ. High concentrations of iron (II) were associated with both fine and coarse aerosol

  9. The distribution and diversity of sea cucumbers in the coral reefs of the South China Sea, Sulu Sea and Sulawesi Sea

    NASA Astrophysics Data System (ADS)

    Woo, Sau Pinn; Yasin, Zulfigar; Ismail, Siti Hasmah; Tan, Shau Hwai

    2013-11-01

    A study on the distribution and diversity of sea cucumbers in the coral reefs of the South China Sea, Sulu Sea and Sulawesi Sea was carried out in July 2009. The survey was done using wandering transect underwater with SCUBA. Twelve species of sea cucumber were found from four different families and nine genera. The most dominant family was Holothuriidae (five species), followed by Stichopodidae (three species), Synaptidae (three species) and Cucumariidae with only one species. The most dominant species found around the island was Pearsonothuria graffei, which can be found abundantly on substrate of dead corals in a wide range of depth (6-15 m). The Sulawesi Sea showed a higher diversity of sea cucumber with seven different species compared to the South China Sea with only six different species and Sulu Sea with only two species. Ordination by multidimensional scaling of Bray-Curtis similarities clustered the sampling locations to three main clusters with two outgroups. Previous studies done indicated a higher diversity of sea cucumber as compared to this study. This can be indication that the population and diversity of sea cucumbers in the reef is under threat.

  10. An effective inversion algorithm for retrieving bimodal aerosol particle size distribution from spectral extinction data

    NASA Astrophysics Data System (ADS)

    He, Zhenzong; Qi, Hong; Yao, Yuchen; Ruan, Liming

    2014-12-01

    The Ant Colony Optimization algorithm based on the probability density function (PDF-ACO) is applied to estimate the bimodal aerosol particle size distribution (PSD). The direct problem is solved by the modified Anomalous Diffraction Approximation (ADA, as an approximation for optically large and soft spheres, i.e., χ≫1 and |m-1|≪1) and the Beer-Lambert law. First, a popular bimodal aerosol PSD and three other bimodal PSDs are retrieved in the dependent model by the multi-wavelength extinction technique. All the results reveal that the PDF-ACO algorithm can be used as an effective technique to investigate the bimodal PSD. Then, the Johnson's SB (J-SB) function and the modified beta (M-β) function are employed as the general distribution function to retrieve the bimodal PSDs under the independent model. Finally, the J-SB and M-β functions are applied to recover actual measurement aerosol PSDs over Beijing and Shanghai obtained from the aerosol robotic network (AERONET). The numerical simulation and experimental results demonstrate that these two general functions, especially the J-SB function, can be used as a versatile distribution function to retrieve the bimodal aerosol PSD when no priori information about the PSD is available.

  11. Aerosol Size Distribution in a City Influenced by Both Rural and Urban Regions

    NASA Astrophysics Data System (ADS)

    Fitzgerald, R. M.; Polanco, J.; Lozano, A.

    2006-12-01

    Most atmospheric studies have focused on sites located in either rural or urban areas. However, there are regions affected by air from both, such as the city of El Paso. Adjacent to the neighboring city of Juarez, Mexico, and in close proximity to rural areas, it is affected by desert particles and both biogenic, anthropogenic emissions. Aerosol properties largely depend upon particle size and this makes it the most important parameter for characterizing the aerosol. We focus on studies using inverse reconstruction models for particle size distribution using aerosol optical depth data. Our methodology uses Twomey's regularization technique that suppresses ill-posedness by imposing smoothing and non-negativity constraints on the desired size distributions. We have also applied T-matrix codes to study the scattering from irregularly shaped particles that exhibit rotational symmetry. Furthermore, our studies include analysis of aerosol size distributions using optic probes and soot photometers, sampled from aircraft at different heights. This work will lead to better characterization of aerosols and their impact in our rural-urban interface region. In addition, it will provide a more accurate assessment of regional transport and better boundary conditions for air quality models.

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

    PubMed

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

    2015-09-01

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

  13. Distribution and air-sea fluxes of carbon dioxide on the Chukchi Sea shelf

    NASA Astrophysics Data System (ADS)

    Pipko, I. I.; Pugach, S. P.; Repina, I. A.; Dudarev, O. V.; Charkin, A. N.; Semiletov, I. P.

    2015-12-01

    This article presents the results of long-term studies of the dynamics of carbonate parameters and air-sea carbon dioxide fluxes on the Chukchi Sea shelf during the summer. As a result of the interaction of physical and biological factors, the surface waters on the west of Chukchi Sea were undersaturated with carbon dioxide when compared with atmospheric air; the partial pressure of CO2 varied in the range from 134 to 359 μatm. The average value of CO2 flux in the Chukchi Sea per unit area varied in the range from-2.4 to-22.0 mmol /(m2 day), which is significantly higher than the average value of CO2 flux in the World Ocean. It has been estimated that the minimal mass of C absorbed by the surface of Chukchi Sea from the atmosphere during ice-free season is 13 × 1012 g; a great part of this carbon is transported to the deeper layers of sea and isolated from the atmosphere for a long period of time. The studies of the carbonate system of the Chukchi Sea, especially of its western part, will provide some new data on the fluxes of carbon dioxide in the Arctic Ocean and their changes. Our analysis can be used for an interpretation of the satellite assessment of CO2 fluxes and dissolved CO2 distribution in the upper layers of the ocean.

  14. Nutrients in the Kara Sea: Distribution, Variability, and Budgets.

    NASA Astrophysics Data System (ADS)

    Novikhin, A.

    2003-04-01

    The Kara Sea is located far to the north from the Polar circle on the shallow Siberian shelf. The climate conditions of the sea are severe and the sea is covered by ice during most part of the year. Changeable hydrometeorological, ice, and biological conditions, complicated bottom relief, indented shoreline and numerous islands form a multilayered and mosaic water column structure in the Kara Sea. One of the remarkable features of the Kara Sea is a large continental runoff, which consists of about 40 % of total river runoff into the Arctic seas. The great Siberian rivers Ob and Yenisei transport more than 150 million tones of suspended and dissolved organic and inorganic matter to the sea every year. This additional nutrient influx plays an important ecological role, because it stimulates primary production. The river runoff is one of the main sources of the terrestrial organic matter for the Kara Sea. To study nutrient variability and distributions the data set from the US-Russian Electronic Hydrochemical Atlas of the Arctic Ocean which containing more than 15000 stations from 1906 till 2000 and the new data, obtained in the Russian-German expeditions were used. The main results of the studies of nutrient spatial and temporal variability in the river plume area and also in the deep troughs St. Anna, Voronin, and Novozemelsky are reported. Nutrient budgeting studies in the Ob and Yenisei estuaries reveal that the Ob Gulf is net production of inorganic nitrogen and phosphorus. The Yenisei Gulf is net removal of inorganic nitrogen and phosphorus during the year.

  15. Updating sea spray aerosol emissions in the Community Multiscale Air Quality (CMAQ) model version 5.0.2

    NASA Astrophysics Data System (ADS)

    Gantt, B.; Kelly, J. T.; Bash, J. O.

    2015-11-01

    Sea spray aerosols (SSAs) impact the particle mass concentration and gas-particle partitioning in coastal environments, with implications for human and ecosystem health. Model evaluations of SSA emissions have mainly focused on the global scale, but regional-scale evaluations are also important due to the localized impact of SSAs on atmospheric chemistry near the coast. In this study, SSA emissions in the Community Multiscale Air Quality (CMAQ) model were updated to enhance the fine-mode size distribution, include sea surface temperature (SST) dependency, and reduce surf-enhanced emissions. Predictions from the updated CMAQ model and those of the previous release version, CMAQv5.0.2, were evaluated using several coastal and national observational data sets in the continental US. The updated emissions generally reduced model underestimates of sodium, chloride, and nitrate surface concentrations for coastal sites in the Bay Regional Atmospheric Chemistry Experiment (BRACE) near Tampa, Florida. Including SST dependency to the SSA emission parameterization led to increased sodium concentrations in the southeastern US and decreased concentrations along parts of the Pacific coast and northeastern US. The influence of sodium on the gas-particle partitioning of nitrate resulted in higher nitrate particle concentrations in many coastal urban areas due to increased condensation of nitric acid in the updated simulations, potentially affecting the predicted nitrogen deposition in sensitive ecosystems. Application of the updated SSA emissions to the California Research at the Nexus of Air Quality and Climate Change (CalNex) study period resulted in a modest improvement in the predicted surface concentration of sodium and nitrate at several central and southern California coastal sites. This update of SSA emissions enabled a more realistic simulation of the atmospheric chemistry in coastal environments where marine air mixes with urban pollution.

  16. Saharan dust aerosol over the central Mediterranean Sea: optical columnar measurements vs. aerosol load, chemical composition and marker solubility at ground level

    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.

    2013-08-01

    This study aims at the determination of the mineral contribution to PM10 in the central Mediterranean Sea on the basis of 7 yr of PM10 chemical composition daily measurements made on the island of Lampedusa (35.5° N, 12.6° E). Aerosol optical depth measurements are carried out in parallel while sampling with a multi-stage impactor, and observations with an optical particle counter were performed in selected periods. Based on daily samples, the total content and soluble fraction of selected metals are used to identify and characterize the dust events. The total contribution is determined by PIXE (particle-induced X-ray emission) while the composition of the soluble fraction by ICP-AES (inductively coupled plasma atomic emission spectroscopy) after extraction with HNO3 at pH 1.5. The average PM10 concentration at Lampedusa calculated 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 exceed 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 with crustal content exceeding the 75th percentile of the crustal oxide content distribution were identified as dust events. Using this threshold we identify 175 events; 31.6% of them (55 events) present PM10 higher than 50 μg m-3, with dust contributing by 33% on average. The annual average crustal contribution to PM10 is 5.42 μg m-3, reaching a value as high as 67.9 μg m-3, 49% of PM10, during an intense Saharan dust event. The crustal aerosol amount and contribution to PM10 shows a very small seasonal dependence; conversely, the dust columnar burden displays an evident annual cycle, with a strong summer maximum (monthly

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

    NASA Technical Reports Server (NTRS)

    Deshler, Terry; Hervig, Mark E.

    1998-01-01

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

  18. Future fish distributions constrained by depth in warming seas

    NASA Astrophysics Data System (ADS)

    Rutterford, Louise A.; Simpson, Stephen D.; Jennings, Simon; Johnson, Mark P.; Blanchard, Julia L.; Schön, Pieter-Jan; Sims, David W.; Tinker, Jonathan; Genner, Martin J.

    2015-06-01

    European continental shelf seas have experienced intense warming over the past 30 years. In the North Sea, fish have been comprehensively monitored throughout this period and resulting data provide a unique record of changes in distribution and abundance in response to climate change. We use these data to demonstrate the remarkable power of generalized additive models (GAMs), trained on data earlier in the time series, to reliably predict trends in distribution and abundance in later years. Then, challenging process-based models that predict substantial and ongoing poleward shifts of cold-water species, we find that GAMs coupled with climate projections predict future distributions of demersal (bottom-dwelling) fish species over the next 50 years will be strongly constrained by availability of habitat of suitable depth. This will lead to pronounced changes in community structure, species interactions and commercial fisheries, unless individual acclimation or population-level evolutionary adaptations enable fish to tolerate warmer conditions or move to previously uninhabitable locations.

  19. A Comprehensive Archive of Aerosol and Trace Gas Spatial Distributions for Model and Satellite Validation

    NASA Astrophysics Data System (ADS)

    Wilson, J. C.; Meland, B. S.; Axisa, D.

    2015-12-01

    The University of Denver Aerosol Group has assembled measured aerosol size distributions, gaseous concentrations, and atmospheric state variables covering a 30 year time period into one comprehensive archive. Measurements were made during the period 1987-2013 and include data from a total of 21 NASA field campaigns. Measurements were taken from the ground to over 21 km in altitude, from 72 S Latitude to 90 N latitude on over 300 individual flights on NASA Research Aircraft. Aerosol measurements were made with the University of Denver's Nucleation-Mode Aerosol Size Spectrometer (NMASS), Focused Cavity Aerosol Spectrometer, and/or a low-pressure Condensation Particle Counter (CPC) depending on the specific campaign. The science payloads varied with the campaign objectives, but the aerosol data were invariably acquired in conjunction with measurements by other investigators placing them in the context of atmospheric composition. The archive includes location and time of the measurements along with the tropopause heights and selected atmospheric composition and state data such as ambient temperatures and pressures, abundances of ozone, N2O, oxides of nitrogen, water vapor, CO2 etc. The data archive is stored in NetCDF format and includes all relevant metadata for measured quantities. This archive will be hosted by NASA and will be available to the public for model validation. The data includes indexing by scientific campaign, date, and spatial coordinates. This will facilitate comparisons across the available range of times, locations and related measurements. This data set has been used for validation of satellite remote sensing data. Coincident measurements of aerosol size distributions were used to calculate extinction profiles which were compared to those retrieved with the SAGE II satellite. Agreement between extinctions derived from the in situ size measurements and those provided by SAGE II was good for the 452, 525, and 1020 nm wavelength channels, but poor for

  20. On numerical simulation of the global distribution of sulfate aerosol produced by a large volcanic eruption

    SciTech Connect

    Pudykiewicz, J.A.; Dastoor, A.P.

    1994-12-31

    Volcanic eruptions play an important role in the global sulfur cycle of the Earth`s atmosphere and can significantly perturb the global atmospheric chemistry. The large amount of sulfate aerosol produced by the oxidation of SO{sub 2} injected into the atmosphere during volcanic eruptions also has a relatively big influence on the radiative equilibrium of the Earth`s climatic system. The submicron particles of the sulfate aerosol reflect solar radiation more effectively than they trap radiation in the infrared range. The effect of this is observed as cooling of the Earth`s surface. The modification of the global radiation budget following volcanic eruption can subsequently cause significant fluctuations of atmospheric variables on a subclimatic scale. The resulting perturbation of weather patterns has been observed and well documented since the eruptions of Mt. Krakatau and Mt. Tambora. The impact of the sulfate aerosol from volcanic eruptions on the radiative equilibrium of the Earth`s atmosphere was also confirmed by the studies done with Global Circulation Models designed to simulate climate. The objective of the present paper is to present a simple and effective method to estimate the global distribution of the sulfate aerosol produced as a consequence of volcanic eruptions. In this study we will present results of the simulation of global distribution of sulfate aerosol from the eruption of Mt Pinatubo.

  1. [Characteristics of Number Concentration Size Distributions of Aerosols Under Processes in Beijing].

    PubMed

    Su, Jie; Zhao, Pu-sheng; Chen, Yi-na

    2016-04-15

    The aerosol number concentration size distributions were measured by a Wide-Range Particle Spectrometer (WPS-1000XP) at an urban site of Beijing from 2012 to 2014; and the characteristics of the size distributions in different seasons and weather conditions were discussed. The results showed that the daily average number concentration of Aitken mode aerosols was highest in the spring and lowest in the autumn; the daily average number concentration of accumulation mode aerosols was bigher in the spring and winter, while lowest in summer; and the average concentration of coarse mode was highest during the winter. The Aitken mode particles had the most significant diurnal variations resulted from the traffic sources and the summer photochemical reactions. In the spring, autumn and winter, the number concentrations of accumulation mode of the nighttime was higher than that of the daytime. The coarse mode particles did not have obvious diurnal variation. During the heavy pollution process, the accumulation mode aerosols played a decisive role in PM₂.₅ concentrations and was usually removed by the north wind. The precipitation could effectively eliminate the coarse mode particles, but it bad no obvious effect on the accumulation mode particles under small speed wind and zero speed wind. During the dust process, the concentrations of coarse mode particles increased significantly, while the accumulation mode aerosol concentration was obviously decreased. PMID:27548939

  2. The aerosol distribution in Uranus' atmosphere - Interpretation of the hydrogen spectrum

    NASA Technical Reports Server (NTRS)

    Trafton, L.

    1976-01-01

    New observations of Uranus' combined H2 spectrum have been obtained. An analysis, emphasizing the leverage provided by the S3(0) quadrupole line, leads to strong constraints on Uranus' bulk aerosol distribution with depth. Using an inhomogeneous model atmosphere program which includes Rayleigh scattering for gases and a 1 plus cos theta phase function for cloud layers, it is shown that Uranus' H2 spectrum implies a cloud layer (or dense aerosol) at a depth from 500 to 700 km-amagat H2. It also implies negligible aerosol scattering in the 280 to 450 km-amagat H2 region and a thin haze at 100 to 200 km-amagat H2 depths. The low albedo in very strong CH4 bands indicates that there is negligible aerosol scattering in Uranus' radiative zone. Hydrogen appears to be more abundant than the sum of all other atmospheric gases. The C/H ratio deep in Uranus' atmosphere is strongly enhanced over the solar value. Accurate limb-darkening measurements in and near strong CH4 bands would be effective in specifying Uranus' aerosol distribution in greater detail.

  3. Application of the TDMA Technique Toward the Size and Charge Distribution Measurement of Graphite, Gold, Palladium, and Silver Aerosols

    NASA Astrophysics Data System (ADS)

    Simones, Matthew Paul

    The knowledge of charge distributions among aerosol particles has been an important topic for many years because of the strong electrostatic interactions which can greatly influence aerosol transport and evolution. Theoretical models have been developed although experimental verification has been limited because of the difficulty in measuring charged aerosols. Recently a method utilizing a tandem differential mobility analyzer (TDMA) has been shown to be applicable toward measuring both the size and charge distributions of nanosized combustion aerosols. The goal of this work is on further exploration of this method toward the measurement of non-combustion aerosols and in particular those associated with very high temperature reactors (VHTRs). The complete bipolar charge and size distributions of spark generated graphite, gold, silver, and palladium aerosol have been measured with a TDMA apparatus assembled and calibrated during this study. In addition, an electrostatic precipitator has been designed and constructed for measuring the size distributions of neutrally charged particles associated with these aerosols. The results show charge asymmetry in all measured aerosols with higher concentrations of positively charged particles than negative at the same charge level. These results differ from equilibrium charge distributions of both Boltzmann and Fuchs showing that charge equilibrium may not always be an appropriate assumption. The TDMA technique should find applications in characterizing VHTR aerosols and rate processes such as coagulation, deposition, and resuspension which will be important for both reactor design, and accident modeling and simulation.

  4. Characterizing the Spatial and Temporal Distribution of Aerosol Optical Thickness Over the Atlantic Basin Utilizing GOES-8 Multispectral Data

    NASA Technical Reports Server (NTRS)

    Fox, Robert; Prins, Elaine Mae; Feltz, Joleen M.

    2001-01-01

    In recent years, modeling and analysis efforts have suggested that the direct and indirect radiative effects of both anthropogenic and natural aerosols play a major role in the radiative balance of the earth and are an important factor in climate change calculations. The direct effects of aerosols on radiation and indirect effects on cloud properties are not well understood at this time. In order to improve the characterization of aerosols within climate models it is important to accurately parameterize aerosol forcing mechanisms at the local, regional, and global scales. This includes gaining information on the spatial and temporal distribution of aerosols, transport regimes and mechanisms, aerosol optical thickness, and size distributions. Although there is an expanding global network of ground measurements of aerosol optical thickness and size distribution at specific locations, satellite data must be utilized to characterize the spatial and temporal extent of aerosols and transport regimes on regional and global scales. This study was part of a collaborative effort to characterize aerosol radiative forcing over the Atlantic basin associated with the following three major aerosol components in this region: urban/sulfate, Saharan dust, and biomass burning. In-situ ground measurements obtained by a network of sun photometers during the Smoke Clouds and Radiation Experiment in Brazil (SCAR-B) and the Tropospheric Aerosol Radiative Forcing Observational Experiment (TARFOX) were utilized to develop, calibrate, and validate a Geostationary Operational Environmental Satellite (GOES)-8 aerosol optical thickness (AOT) product. Regional implementation of the GOES-8 AOT product was used to augment point source measurements to gain a better understanding of the spatial and temporal distributions of Atlantic basin aerosols during SCAR-B and TARFOX.

  5. "Chlorine explosion" from sea-salt aerosols in a polluted atmosphere

    NASA Astrophysics Data System (ADS)

    Buxmann, Joelle; Bleicher, Sergej; Zetzsch, Cornelius; Platt, Ulrich

    2013-04-01

    Bromine and chlorine 'explosions' (BE and CE) refer to autocatalytic, heterogeneous releases of reactive halogen species (RHS). ClO and BrO play a key role as RHS, as they influence the tropospheric oxidation capacity through destruction of ozone and fast reactions with nitrogen oxides. Besides OH radicals, Cl atoms react at a fast rate with the greenhouse gas methane, but the global effect is not clear yet. From smog-chamber experiments under tropospheric light conditions, ClO, OClO (from CE) and BrO (from BE) released from artificial sea salt aerosols were detected using a White system in combination with Differential Optical Absorption Spectroscopy (DOAS). Up to 17 ppb of ClO, 6 ppb of OClO and 1.6 ppb of BrO were observed under the influence of high NO2 and O3 concentrations. The RHS activation is triggered by NO2 reactions starting during the dark period. Formation of ClNO2 and ClONO2 and acidification of the aerosol by HNO3 or HONO play key roles. The lifetime of Cl2 of 645 s against photolysis in our smog chamber was estimated to be longer than the uptake onto the aerosol surface with a lifetime of 83s. The fact that Cl2 photolysis is slower compared to uptake, indicates that Cl2 might not be sufficient as a precursor for the observed ClO and OClO mixing rations during the chamber experiments at high NOx. Furthermore, OClO ( 40ppt/s) is formed at a faster rate than ClO ( 15ppt/s) in our experiments. A simple model, including the known gas phase reactions of halogen oxides, O3 and NOx, predicts the maximum ClO concentration to occur before the maximum OClO concentration. The measurement indicates the opposite. This suggests heterogeneous OClO formation. The lifetime of OClO against photolysis is only 20s in our chamber. But an actual heterogeneous release mechanism to form OClO has not been confirmed yet. Nevertheless, these results suggest that OClO is important for the heterogeneous release process. While BE has been demonstrated to occur in nature, the

  6. Vertical distribution of picoeukaryotic diversity in the Sargasso Sea.

    PubMed

    Not, Fabrice; Gausling, Rudolf; Azam, Farooq; Heidelberg, John F; Worden, Alexandra Z

    2007-05-01

    Eukaryotic molecular diversity within the picoplanktonic size-fraction has primarily been studied in marine surface waters. Here, the vertical distribution of picoeukaryotic diversity was investigated in the Sargasso Sea from euphotic to abyssal waters, using size-fractionated samples (< 2 microm). 18S rRNA gene clone libraries were used to generate sequences from euphotic zone samples (deep chlorophyll maximum to the surface); the permanent thermocline (500 m); and the pelagic deep-sea (3000 m). Euphotic zone and deep-sea data contrasted strongly, the former displaying greater diversity at the first-rank taxon level, based on 232 nearly full-length sequences. Deep-sea sequences belonged almost exclusively to the Alveolata and Radiolaria, while surface samples also contained known and putative photosynthetic groups, such as unique Chlorarachniophyta and Chrysophyceae sequences. Phylogenetic analyses placed most Alveolata and Stramenopile sequences within previously reported 'environmental' clades, i.e. clades within the Novel Alveolate groups I and II (NAI and NAII), or the novel Marine Stramenopiles (MAST). However, some deep-sea NAII formed distinct, bootstrap supported clades. Stramenopiles were recovered from the euphotic zone only, although many MAST are reportedly heterotrophic, making the observed distribution a point for further investigation. An unexpectedly high proportion of radiolarian sequences were recovered. From these, five environmental radiolarian clades, RAD-I to RAD-V, were identified. RAD-IV and RAD-V were composed of Taxopodida-like sequences, with the former solely containing Sargasso Sea sequences, although from all depth zones sampled. Our findings highlight the vast diversity of these protists, most of which remain uncultured and of unknown ecological function.

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

    DOE PAGES

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

    2013-01-01

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

  8. Latitudinal and longitudinal variation in aerosol characteristics from Sun photometer and MODIS over the Bay of Bengal and Arabian Sea during ICARB

    NASA Astrophysics Data System (ADS)

    Kedia, Sumita; Ramachandran, S.

    2008-07-01

    Spatial variations in aerosol optical properties as function of latitude and longitude are analysed over the Bay of Bengal and Arabian Sea during ICARB cruise period of March-May 2006 from in situ sun photometer and MODIS (Terra, Aqua) satellite measurements. Monthly mean 550 nm aerosol optical depths (AODs) over the Bay of Bengal and Arabian Sea show an increase from March to May both in spatial extent and magnitude. AODs are found to increase with latitude from 4°N to 20°N over the Bay of Bengal while over Arabian Sea, variations are not significant. Sun photometer and MODIS AODs agree well within ±1σ variation. Bay of Bengal AOD (0.28) is higher than the Arabian Sea (0.24) latitudinally. Aerosol fine mode fraction (FMF) is higher than 0.6 over Bay of Bengal, while FMF in the Arabian Sea is about 0.5. Bay of Bengal α(˜1) is higher than the Arabian Sea value of 0.7, suggesting the dominance of fine mode aerosols over Bay of Bengal which is corroborated by higher FMF values over Bay of Bengal. Air back trajectory analyses suggest that aerosols from different source regions contribute differently to the optical characteristics over the Bay of Bengal and Arabian Sea.

  9. Processes controlling the annual cycle of Arctic aerosol number and size distributions

    NASA Astrophysics Data System (ADS)

    Croft, Betty; Martin, Randall V.; Leaitch, W. Richard; Tunved, Peter; Breider, Thomas J.; D'Andrea, Stephen D.; Pierce, Jeffrey R.

    2016-03-01

    Measurements at high-Arctic sites (Alert, Nunavut, and Mt. Zeppelin, Svalbard) during the years 2011 to 2013 show a strong and similar annual cycle in aerosol number and size distributions. Each year at both sites, the number of aerosols with diameters larger than 20 nm exhibits a minimum in October and two maxima, one in spring associated with a dominant accumulation mode (particles 100 to 500 nm in diameter) and a second in summer associated with a dominant Aitken mode (particles 20 to 100 nm in diameter). Seasonal-mean aerosol effective diameter from measurements ranges from about 180 in summer to 260 nm in winter. This study interprets these annual cycles with the GEOS-Chem-TOMAS global aerosol microphysics model. Important roles are documented for several processes (new-particle formation, coagulation scavenging in clouds, scavenging by precipitation, and transport) in controlling the annual cycle in Arctic aerosol number and size. Our simulations suggest that coagulation scavenging of interstitial aerosols in clouds by aerosols that have activated to form cloud droplets strongly limits the total number of particles with diameters less than 200 nm throughout the year. We find that the minimum in total particle number in October can be explained by diminishing new-particle formation within the Arctic, limited transport of pollution from lower latitudes, and efficient wet removal. Our simulations indicate that the summertime-dominant Aitken mode is associated with efficient wet removal of accumulation-mode aerosols, which limits the condensation sink for condensable vapours. This in turn promotes new-particle formation and growth. The dominant accumulation mode during spring is associated with build up of transported pollution from outside the Arctic coupled with less-efficient wet-removal processes at colder temperatures. We recommend further attention to the key processes of new-particle formation, interstitial coagulation, and wet removal and their delicate

  10. Interannual variability of monthly Southern Ocean sea ice distributions

    NASA Technical Reports Server (NTRS)

    Parkinson, Claire L.

    1992-01-01

    The interannual variability of the Southern-Ocean sea-ice distributions was mapped and analyzed using data from Nimbus-5 ESMR and Nimbus-7 SMMR, collected from 1973 to 1987. The set of 12 monthly maps obtained reveals many details on spatial variability that are unobtainable from time series of ice extents. These maps can be used as baseline maps for comparisons against future Southern Ocean sea ice distributions. The maps are supplemented by more detailed maps of the frequency of ice coverage, presented in this paper for one month within each of the four seasons, and by the breakdown of these results to the periods covered individually by each of the two passive-microwave imagers.

  11. Microbial Control of Sea Spray Aerosol Composition: A Tale of Two Blooms.

    PubMed

    Wang, Xiaofei; Sultana, Camille M; Trueblood, Jonathan; Hill, Thomas C J; Malfatti, Francesca; Lee, Christopher; Laskina, Olga; Moore, Kathryn A; Beall, Charlotte M; McCluskey, Christina S; Cornwell, Gavin C; Zhou, Yanyan; Cox, Joshua L; Pendergraft, Matthew A; Santander, Mitchell V; Bertram, Timothy H; Cappa, Christopher D; Azam, Farooq; DeMott, Paul J; Grassian, Vicki H; Prather, Kimberly A

    2015-06-24

    With the oceans covering 71% of the Earth, sea spray aerosol (SSA) particles profoundly impact climate through their ability to scatter solar radiation and serve as seeds for cloud formation. The climate properties can change when sea salt particles become mixed with insoluble organic material formed in ocean regions with phytoplankton blooms. Currently, the extent to which SSA chemical composition and climate properties are altered by biological processes in the ocean is uncertain. To better understand the factors controlling SSA composition, we carried out a mesocosm study in an isolated ocean-atmosphere facility containing 3,400 gallons of natural seawater. Over the course of the study, two successive phytoplankton blooms resulted in SSA with vastly different composition and properties. During the first bloom, aliphatic-rich organics were enhanced in submicron SSA and tracked the abundance of phytoplankton as indicated by chlorophyll-a concentrations. In contrast, the second bloom showed no enhancement of organic species in submicron particles. A concurrent increase in ice nucleating SSA particles was also observed only during the first bloom. Analysis of the temporal variability in the concentration of aliphatic-rich organic species, using a kinetic model, suggests that the observed enhancement in SSA organic content is set by a delicate balance between the rate of phytoplankton primary production of labile lipids and enzymatic induced degradation. This study establishes a mechanistic framework indicating that biological processes in the ocean and SSA chemical composition are coupled not simply by ocean chlorophyll-a concentrations, but are modulated by microbial degradation processes. This work provides unique insight into the biological, chemical, and physical processes that control SSA chemical composition, that when properly accounted for may explain the observed differences in SSA composition between field studies. PMID:27162962

  12. An improved whitecap timescale for sea spray aerosol production flux modeling using the discrete whitecap method

    NASA Astrophysics Data System (ADS)

    Callaghan, Adrian H.

    2013-09-01

    The discrete whitecap method (DWM) to model the sea spray aerosol (SSA) production flux explicitly requires a whitecap timescale, which up to now has only considered a whitecap decay timescale, τdecay. A reevaluation of the DWM suggests that the whitecap timescale should account for the total whitecap lifetime (τwcap), which consists of both the formation timescale (τform) and the decay timescale (timescale definitions are given in the text). Here values of τform for 552 oceanic whitecaps measured at the Martha's Vineyard Coastal Observatory on the east coast of the USA are presented, and added to the corresponding values of τdecay to form 552 whitecap timescales. For the majority of whitecaps, τform makes up about 20-25% of τwcap, but this can be as large as 70% depending on the value of τdecay. Furthermore, an area-weighted mean whitecap timescale for use in the DWM (τDWM) is defined that encompasses the variable nature of individual whitecap lifetimes within a given time period, and is calculated to be 5.3 s for this entire data set. This value is combined with previously published whitecap coverage parameterizations and estimates of SSA particle production per whitecap area to form a size-resolved SSA production flux parameterization (dF(r80)/dlog10r80). This parameterization yields integrated sea-salt mass fluxes that are largely within the range of uncertainty of recent measurements over the size range 0.029 µm < r80 < 0.580 µm. Physical factors controlling whitecap lifetime such as bubble plume lifetime and surfactant stabilization are discussed in the context of SSA production from whitecaps.

  13. LASE Measurements of Water Vapor, Aerosol, and Cloud Distributions in Saharan Air Layers and Tropical Disturbances

    NASA Technical Reports Server (NTRS)

    Ismail, Syed; Ferrare, Richard A.; Browell, Edward V.; Kooi, Susan A.; Dunion, Jason P.; Heymsfield, Gerry; Notari, Anthony; Butler, Carolyn F.; Burton, Sharon; Fenn, Marta; Krishnamurti, T. N.; Chen, Gao; Anderson, Bruce

    2010-01-01

    LASE (Lidar Atmospheric Sensing Experiment) on-board the NASA DC-8 measured high resolution profiles of water vapor and aerosols, and cloud distributions in 14 flights over the eastern North Atlantic during the NAMMA (NASA African Monsoon Multidisciplinary Analyses) field experiment. These measurements were used to study African easterly waves (AEWs), tropical cyclones (TCs), and the Saharan Air Layer(s) (SAL). Interactions between the SAL and tropical air were observed during the early stages of the TC development. These LASE measurements represent the first simultaneous water vapor and aerosol lidar measurements to study the SAL and its impact on AEWs and TCs. Examples of profile measurements of aerosol scattering ratios, aerosol extinction coefficients, aerosol optical thickness, water vapor mixing ratios, RH, and temperature are presented to illustrate their characteristics in SAL, convection, and clear air regions. LASE data suggest that the SAL suppresses low-altitude convection at the convection-SAL interface region. Mid-level convection associated with the AEW and transport are likely responsible for high water vapor content observed in the southern regions of the SAL on August 20, 2008. This interaction is responsible for the transfer of about 7 x 10(exp 15) J latent heat energy within a day to the SAL. Measurements of lidar extinction-to-backscatter ratios in the range 36+/-5 to 45+/-5 are within the range of measurements from other lidar measurements of dust. LASE aerosol extinction and water vapor profiles are validated by comparison with onboard in situ aerosol measurements and GPS dropsonde water vapor soundings, respectively.

  14. Seasonal, intraseasonal, and interannual variability of global land fires and their effects on atmospheric aerosol distribution

    NASA Astrophysics Data System (ADS)

    Ji, Yimin; Stocker, Erich

    2002-12-01

    In order to understand the variability of global land fires and their effects on the distribution of atmospheric aerosols, statistical methods were applied to the Tropical Rainfall Measuring Mission (TRMM) fire products as well as the Total Ozone Mapping Spectrometer (TOMS) aerosol index products for a period of 4 years from January 1998 to December 2001. The fire data in this period manifested a strong annual cycle of land fires in Southeast Asia with a peak in March and in Africa and North and South America with a peak in August. The data also indicated interannual variations in Indonesia and Central America associated with the 1998-1999 El Niño-Southern Oscillation cycle. The variability of global atmospheric aerosol is consistent with the fire variations over these regions. However, in southwestern Australia, intense fires were recorded in TRMM fire data, but no smoke was observed in the TOMS aerosol product. Excluding the Australian region, the correlation between fire count and TOMS aerosol index is about 0.55 for fire pixels. Empirical orthogonal function analysis (EOF) and singular spectrum analysis methods were used to analyze the TRMM Science Data and Information System pentad fire composite data and TOMS pentad aerosol index data for this 4 year period. The EOF analyses showed contrast between the Northern and Southern Hemispheres and also intercontinental transitions in Africa and America. These analyses also identified 25-60 day intraseasonal oscillations that were superimposed on the annual cycles of both fire and aerosol data. The intraseasonal variability of fires showed a similarity of Madden-Julian oscillation mode.

  15. Size distribution dynamics reveal particle-phase chemistry in organic aerosol formation.

    PubMed

    Shiraiwa, Manabu; Yee, Lindsay D; Schilling, Katherine A; Loza, Christine L; Craven, Jill S; Zuend, Andreas; Ziemann, Paul J; Seinfeld, John H

    2013-07-16

    Organic aerosols are ubiquitous in the atmosphere and play a central role in climate, air quality, and public health. The aerosol size distribution is key in determining its optical properties and cloud condensation nucleus activity. The dominant portion of organic aerosol is formed through gas-phase oxidation of volatile organic compounds, so-called secondary organic aerosols (SOAs). Typical experimental measurements of SOA formation include total SOA mass and atomic oxygen-to-carbon ratio. These measurements, alone, are generally insufficient to reveal the extent to which condensed-phase reactions occur in conjunction with the multigeneration gas-phase photooxidation. Combining laboratory chamber experiments and kinetic gas-particle modeling for the dodecane SOA system, here we show that the presence of particle-phase chemistry is reflected in the evolution of the SOA size distribution as well as its mass concentration. Particle-phase reactions are predicted to occur mainly at the particle surface, and the reaction products contribute more than half of the SOA mass. Chamber photooxidation with a midexperiment aldehyde injection confirms that heterogeneous reaction of aldehydes with organic hydroperoxides forming peroxyhemiacetals can lead to a large increase in SOA mass. Although experiments need to be conducted with other SOA precursor hydrocarbons, current results demonstrate coupling between particle-phase chemistry and size distribution dynamics in the formation of SOAs, thereby opening up an avenue for analysis of the SOA formation process.

  16. Sustained distribution of aerosolized PEGylated liposomes in epithelial lining fluids on alveolar surfaces.

    PubMed

    Kaneko, Keita; Togami, Kohei; Yamamoto, Eri; Wang, Shujun; Morimoto, Kazuhiro; Itagaki, Shirou; Chono, Sumio

    2016-10-01

    The distribution characteristics of aerosolized PEGylated liposomes in alveolar epithelial lining fluid (ELF) were examined in rats, and the ensuing mechanisms were investigated in the in vitro uptake and protein adsorption experiments. Nonmodified or PEGylated liposomes (particle size 100 nm) were aerosolized into rat lungs. PEGylated liposomes were distributed more sustainably in ELFs than nonmodified liposomes. Furthermore, the uptake of PEGylated liposomes by alveolar macrophages (AMs) was less than that of nonmodified liposomes. In further in vitro uptake experiments, nonmodified and PEGylated liposomes were opsonized with rat ELF components and then added to NR8383 cells as cultured rat AMs. The uptake of opsonized PEGylated liposomes by NR8383 cells was lower than that of opsonized nonmodified liposomes. Moreover, the protein absorption levels in opsonized PEGylated liposomes were lower than those in opsonized nonmodified liposomes. These findings suggest that sustained distributions of aerosolized PEGylated liposomes in ELFs reflect evasion of liposomal opsonization with surfactant proteins and consequent reductions in uptake by AMs. These data indicate the potential of PEGylated liposomes as aerosol-based drug delivery system that target ELF for the treatment of respiratory diseases.

  17. Size distribution dynamics reveal particle-phase chemistry in organic aerosol formation.

    PubMed

    Shiraiwa, Manabu; Yee, Lindsay D; Schilling, Katherine A; Loza, Christine L; Craven, Jill S; Zuend, Andreas; Ziemann, Paul J; Seinfeld, John H

    2013-07-16

    Organic aerosols are ubiquitous in the atmosphere and play a central role in climate, air quality, and public health. The aerosol size distribution is key in determining its optical properties and cloud condensation nucleus activity. The dominant portion of organic aerosol is formed through gas-phase oxidation of volatile organic compounds, so-called secondary organic aerosols (SOAs). Typical experimental measurements of SOA formation include total SOA mass and atomic oxygen-to-carbon ratio. These measurements, alone, are generally insufficient to reveal the extent to which condensed-phase reactions occur in conjunction with the multigeneration gas-phase photooxidation. Combining laboratory chamber experiments and kinetic gas-particle modeling for the dodecane SOA system, here we show that the presence of particle-phase chemistry is reflected in the evolution of the SOA size distribution as well as its mass concentration. Particle-phase reactions are predicted to occur mainly at the particle surface, and the reaction products contribute more than half of the SOA mass. Chamber photooxidation with a midexperiment aldehyde injection confirms that heterogeneous reaction of aldehydes with organic hydroperoxides forming peroxyhemiacetals can lead to a large increase in SOA mass. Although experiments need to be conducted with other SOA precursor hydrocarbons, current results demonstrate coupling between particle-phase chemistry and size distribution dynamics in the formation of SOAs, thereby opening up an avenue for analysis of the SOA formation process. PMID:23818634

  18. Sustained distribution of aerosolized PEGylated liposomes in epithelial lining fluids on alveolar surfaces.

    PubMed

    Kaneko, Keita; Togami, Kohei; Yamamoto, Eri; Wang, Shujun; Morimoto, Kazuhiro; Itagaki, Shirou; Chono, Sumio

    2016-10-01

    The distribution characteristics of aerosolized PEGylated liposomes in alveolar epithelial lining fluid (ELF) were examined in rats, and the ensuing mechanisms were investigated in the in vitro uptake and protein adsorption experiments. Nonmodified or PEGylated liposomes (particle size 100 nm) were aerosolized into rat lungs. PEGylated liposomes were distributed more sustainably in ELFs than nonmodified liposomes. Furthermore, the uptake of PEGylated liposomes by alveolar macrophages (AMs) was less than that of nonmodified liposomes. In further in vitro uptake experiments, nonmodified and PEGylated liposomes were opsonized with rat ELF components and then added to NR8383 cells as cultured rat AMs. The uptake of opsonized PEGylated liposomes by NR8383 cells was lower than that of opsonized nonmodified liposomes. Moreover, the protein absorption levels in opsonized PEGylated liposomes were lower than those in opsonized nonmodified liposomes. These findings suggest that sustained distributions of aerosolized PEGylated liposomes in ELFs reflect evasion of liposomal opsonization with surfactant proteins and consequent reductions in uptake by AMs. These data indicate the potential of PEGylated liposomes as aerosol-based drug delivery system that target ELF for the treatment of respiratory diseases. PMID:27334278

  19. Size distribution dynamics reveal particle-phase chemistry in organic aerosol formation

    PubMed Central

    Shiraiwa, Manabu; Yee, Lindsay D.; Schilling, Katherine A.; Loza, Christine L.; Craven, Jill S.; Zuend, Andreas; Ziemann, Paul J.; Seinfeld, John H.

    2013-01-01

    Organic aerosols are ubiquitous in the atmosphere and play a central role in climate, air quality, and public health. The aerosol size distribution is key in determining its optical properties and cloud condensation nucleus activity. The dominant portion of organic aerosol is formed through gas-phase oxidation of volatile organic compounds, so-called secondary organic aerosols (SOAs). Typical experimental measurements of SOA formation include total SOA mass and atomic oxygen-to-carbon ratio. These measurements, alone, are generally insufficient to reveal the extent to which condensed-phase reactions occur in conjunction with the multigeneration gas-phase photooxidation. Combining laboratory chamber experiments and kinetic gas-particle modeling for the dodecane SOA system, here we show that the presence of particle-phase chemistry is reflected in the evolution of the SOA size distribution as well as its mass concentration. Particle-phase reactions are predicted to occur mainly at the particle surface, and the reaction products contribute more than half of the SOA mass. Chamber photooxidation with a midexperiment aldehyde injection confirms that heterogeneous reaction of aldehydes with organic hydroperoxides forming peroxyhemiacetals can lead to a large increase in SOA mass. Although experiments need to be conducted with other SOA precursor hydrocarbons, current results demonstrate coupling between particle-phase chemistry and size distribution dynamics in the formation of SOAs, thereby opening up an avenue for analysis of the SOA formation process. PMID:23818634

  20. Investigation of the spectral reflectance and bidirectional reflectance distribution function of sea foam layer by the Monte Carlo method.

    PubMed

    Ma, L X; Wang, F Q; Wang, C A; Wang, C C; Tan, J Y

    2015-11-20

    Spectral properties of sea foam greatly affect ocean color remote sensing and aerosol optical thickness retrieval from satellite observation. This paper presents a combined Mie theory and Monte Carlo method to investigate visible and near-infrared spectral reflectance and bidirectional reflectance distribution function (BRDF) of sea foam layers. A three-layer model of the sea foam is developed in which each layer is composed of large air bubbles coated with pure water. A pseudo-continuous model and Mie theory for coated spheres is used to determine the effective radiative properties of sea foam. The one-dimensional Cox-Munk surface roughness model is used to calculate the slope density functions of the wind-blown ocean surface. A Monte Carlo method is used to solve the radiative transfer equation. Effects of foam layer thickness, bubble size, wind speed, solar zenith angle, and wavelength on the spectral reflectance and BRDF are investigated. Comparisons between previous theoretical results and experimental data demonstrate the feasibility of our proposed method. Sea foam can significantly increase the spectral reflectance and BRDF of the sea surface. The absorption coefficient of seawater near the surface is not the only parameter that influences the spectral reflectance. Meanwhile, the effects of bubble size, foam layer thickness, and solar zenith angle also cannot be obviously neglected. PMID:26836550

  1. Comparison of aerosol volume size distributions retrieved from ground-based remote sensing measurements with those from an optical particle counter on the ground

    NASA Astrophysics Data System (ADS)

    Kim, B.; Choi, Y.; Ghim, Y.

    2013-12-01

    Both Cimel CE-318 sunphotometer and POM-02 skyradiometer were operated for around 15 months starting from March 2012 as a part of the DRAGON (Distributed Regional Aerosol Gridded Observation Networks) campaign. These two instruments were collocated at the Hankuk_UFS (Hankuk University of Foreign Studies) site of AERONET (AErosol RObotic NETwork,) and the YGN (Yongin) site of SKYNET (SKYradiometer NETwork). We have also measured the particle concentration on the ground using an optical particle counter (Grimm Model 1.108) since the beginning of this year. The measurement site (37.02 °N, 127.16 °E, 167 m above sea level) is located about 35 km southeast of downtown Seoul. We compare the volume size distributions from sunphotometer, skyradiometer, and optical particle counter for the former part of this year. In the retrieval process, AERONET assumes 22 bins for 0.05-15 μm while SKYNET assumes 20 bins for 0.01-20 μm. The optical particle counter measures the particle number concentrations between 0.25 and 32 μm in 31 bins. Since the measurement intervals are different between instruments, we compare the distributions when the measurement time coincides within 5 minutes as well as mean distributions from the instruments. We examine the differences in mode radii and volume concentrations of fine and coarse mode aerosols between instruments.

  2. Comparison of Summer and Winter California Central Valley Aerosol Distributions from Lidar and MODIS Measurements

    NASA Technical Reports Server (NTRS)

    Lewis, Jasper R., Jr.; DeYoung, Russell J.; Chu, D. Allen

    2010-01-01

    Aerosol distributions from two aircraft lidar campaigns conducted in the California Central Valley are compared in order to identify seasonal variations. Aircraft lidar flights were conducted in June 2003 and February 2008. While the PM2.5 concentration is highest in the winter, the aerosol optical depth measured from MODIS is highest in the summer. A seasonal comparison shows that PM2.5 in the winter can exceed summer PM2.5 by 55%, while summer AOD exceeds winter AOD by 43%. Higher temperatures wildfires in the summer produce elevated aerosol layers that are detected by satellite measurements, but not surface particulate matter monitors. Measurements of the boundary layer height from lidar instruments are necessary to incorporate satellite measurements with air quality measurements.

  3. Vertical Distribution of Dust and Water Ice Aerosols from CRISM Limb-geometry Observations

    NASA Technical Reports Server (NTRS)

    Smith, Michael Doyle; Wolff, Michael J.; Clancy, Todd; Kleinbohl, Armin; Murchie, Scott L.

    2013-01-01

    [1] Near-infrared spectra taken in a limb-viewing geometry by the Compact Reconnaissance Imaging Spectrometer for Mars (CRISM) on board the Mars Reconnaissance Orbiter provide a useful tool for probing atmospheric structure. Specifically, the observed radiance as a function of wavelength and height above the limb enables the vertical distribution of both dust and water ice aerosols to be retrieved. More than a dozen sets of CRISM limb observations have been taken so far providing pole-to-pole cross sections, spanning more than a full Martian year. Radiative transfer modeling is used to model the observations taking into account multiple scattering from aerosols and the spherical geometry of the limb observations. Both dust and water ice vertical profiles often show a significant vertical structure for nearly all seasons and latitudes that is not consistent with the well-mixed or Conrath-v assumptions that have often been used in the past for describing aerosol vertical profiles for retrieval and modeling purposes. Significant variations are seen in the retrieved vertical profiles of dust and water ice aerosol as a function of season. Dust typically extends to higher altitudes (approx. 40-50km) during the perihelion season than during the aphelion season (<20km), and the Hellas region consistently shows more dust mixed to higher altitudes than other locations. Detached water ice clouds are common, and water ice aerosols are observed to cap the dust layer in all seasons.

  4. The Remarkable Condensational Growth of Cloud Droplets Grown on Giant Sea-salt Aerosol Particles

    NASA Astrophysics Data System (ADS)

    Jensen, J. B.; Nugent, A. D.

    2015-12-01

    Condensational growth of cloud drops is often assumed to be a well-understood process, using the drop growth equation: After activation of cloud condensation nuclei into cloud drops at cloud base, model studies often assume that drops quickly become dilute and consist of pure water. As a consequence, adiabatic ascent predicts that the growth rate of these drops is inversely proportional to their radius, and consequently that the drop spectrum will narrow with altitude. Here we demonstrate that drop growth on giant sea-salt aerosol particles (GCCN, dry radius > 0.5 μm) behaves very differently. For typical marine stratocumulus updrafts (0.4 m s-1), and for dry radius > 2 μm, these drops typically remain concentrated solution drops, and their condensational growth is so fast that they accelerate away from the main drop peak, and thus very rapidly attain precipitation drop sizes through condensation only. We show how many studies, that have attempted to include the effects of GCCN by initiating large pure water drops at cloud base, may have seriously underestimated the effects of GCCN on warm rain formation. We also speculate on possible solutions to this issue.

  5. Continental pollution in the Western Mediterranean Basin: vertical profiles of aerosol and trace gases measured over the sea during TRAQA 2012 and SAFMED 2013

    NASA Astrophysics Data System (ADS)

    Di Biagio, C.; Doppler, L.; Gaimoz, C.; Grand, N.; Ancellet, G.; Raut, J.-C.; Beekmann, M.; Borbon, A.; Sartelet, K.; Attié, J.-L.; Ravetta, F.; Formenti, P.

    2015-03-01

    In this study we present airborne observations of aerosol and trace gases obtained over the sea in the Western Mediterranean Basin during the TRAQA (TRansport and Air QuAlity) and SAFMED (Secondary Aerosol Formation in the MEDiterranean) campaigns in summers 2012 and 2013. A total of 23 vertical profiles were measured up to 5000 m a.s.l. over an extended area (40-45° N latitude and 2° W-12° E longitude) including the Gulf of Genoa, Southern France, the Gulf of Lion, and the Spanish coast. TRAQA and SAFMED successfully measured a wide range of meteorological conditions which favoured the pollution export from different sources located around the basin. Also, several events of dust outflows were measured during the campaigns. Observations from the present study indicate that continental pollution largely affects the Western Mediterranean both close to coastal regions and in the open sea as far as ~250 km from the coastline. Aerosol layers not specifically linked with Saharan dust outflows are distributed ubiquitously which indicates quite elevated levels of background pollution throughout the Western Basin. The measured aerosol scattering coefficient varies between ~20 and 120 M m-1, while carbon monoxide (CO) and ozone (O3) mixing ratios are in the range of 60-170 and 30-85 ppbv, respectively. Pollution reaches 3000-4000 m in altitude and presents a very complex and highly stratified structure characterized by fresh and aged layers both in the boundary layer and in the free troposphere. Within pollution plumes the measured particle concentration in the Aitken (0.004-0.1 μm) and accumulation (0.1-1.0 μm) modes is between ˜ 100 and 5000-6000 s cm-3 (standard cm-3), which is comparable to the aerosol concentration measured in continental urban areas. Additionally, our measurements indicate the presence of highly concentrated Aitken layers (10 000-15 000 s cm-3) observed both close to the surface and in the free troposphere, possibly linked to the influence of new

  6. 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.

  7. Sea spray aerosol production measured in-situ and in a laboratory high-speed wind-wave tunnel

    NASA Astrophysics Data System (ADS)

    Savelyev, I.; Frick, G.; Anguelova, M. D.; Haus, B. K.

    2012-12-01

    This presentation overviews a series of experiments recently conducted in the open ocean onboard of Research Platform FLIP, as well as in the high speed Air-Sea Interaction Saltwater Tank (ASIST). In both experiments vertical profiles of size-dependent aerosol concentrations (0.01 - 47 μm range) were measured in close proximity to the air-sea interface using Scattering Aerosol Spectrometer and Differential Mobility Analyzer. Within ~7 days of useful open ocean measurements wind speed U10 varied in ~ 3 - 18 m/s range with significant wave height reaching up to ~ 5 m, whereas U10 wind speed equivalent in ASIST varied up to 40 m/s in addition to mechanically superimposed waves of arbitrary amplitudes. In both cases air-sea interface processes were observed with visible and infrared cameras and other standard instrumentation. This study seeks to evaluate the extent to which laboratory data can complement and aid in the analysis of open ocean measurements. The overall goal is to develop better understanding of underlying physical processes of spray production and its near-surface dynamics, which is needed for uncertainty reduction of existing sea spray source function formulations.

  8. Aerosol chemical properties and related pollutants measured in Dongsha Island in the northern South China Sea during 7-SEAS/Dongsha Experiment

    NASA Astrophysics Data System (ADS)

    Chuang, Ming-Tung; Chang, Shuenn-Chin; Lin, Neng-Huei; Wang, Jia-Lin; Sheu, Guey-Rong; Chang, You-Jia; Lee, Chung-Te

    2013-10-01

    Aerosol observations were conducted at Dongsha Island in two batches from 19 to 23 March and 10 to 19 April 2010. Dongsha Island is located in a remote area over the northern South China Sea (SCS), distantly surrounded by southern China, Taiwan, the Philippines, and the Indochinese Peninsula. During the study period, the average PM10 and PM2.5 mass concentrations were 26.5 ± 19.4 and 12.6 ± 6.0 μg m-3, respectively. In particular, a daily PM10 concentration of 94.1 μg m-3 caused by a yellow-dust event originating from the Asian Continent was recorded on 21 March. Other than this event, the PM2.5 and PM10-2.5 daily levels were 7.1 ± 1.2 and 12.6 ± 5.0 μg m-3, respectively, on days without pollution from anthropogenic sources in the surrounding areas. Water-soluble ions (WSIs) were the predominant components that accounted for 58.7% ± 10.5% and 51.1% ± 7.2% of the PM10 and PM2.5 mass. The second most abundant component was carbonaceous content, which accounted for 9.5% ± 4.7% and 17.5% ± 5.3% of PM10 and PM2.5, respectively. SO42- was the most abundant PM2.5 WSI, whereas the Na+ and Cl- pair was the most abundant PM10-2.5 WSI. Based on the U.S. IMPROVE protocol, the resolved carbonaceous fractions were mainly distributed in PM2.5 and influenced by coal combustion, mobile vehicles, and biomass burning. Most of the resolved WSIs in particles were in the liquid phase due to the humid environment around the northern SCS.

  9. 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.

  10. Global Long-Term SeaWiFS Deep Blue Aerosol Products available at NASA GES DISC

    NASA Technical Reports Server (NTRS)

    Shen, Suhung; Sayer, A. M.; Bettenhausen, Corey; Wei, Jennifer C.; Ostrenga, Dana M.; Vollmer, Bruce E.; Hsu, Nai-Yung; Kempler, Steven J.

    2012-01-01

    Long-term climate data records about aerosols are needed in order to improve understanding of air quality, radiative forcing, and for many other applications. The Sea-viewing Wide Field-of-view Sensor (SeaWiFS) provides a global well-calibrated 13- year (1997-2010) record of top-of-atmosphere radiance, suitable for use in retrieval of atmospheric aerosol optical depth (AOD). Recently, global aerosol products derived from SeaWiFS with Deep Blue algorithm (SWDB) have become available for the entire mission, as part of the NASA Making Earth Science data records for Use in Research for Earth Science (MEaSUREs) program. The latest Deep Blue algorithm retrieves aerosol properties not only over bright desert surfaces, but also vegetated surfaces, oceans, and inland water bodies. Comparisons with AERONET observations have shown that the data are suitable for quantitative scientific use [1],[2]. The resolution of Level 2 pixels is 13.5x13.5 km2 at the center of the swath. Level 3 daily and monthly data are composed by using best quality level 2 pixels at resolution of both 0.5ox0.5o and 1.0ox1.0o. Focusing on the southwest Asia region, this presentation shows seasonal variations of AOD, and the result of comparisons of 5-years (2003- 2007) of AOD from SWDB (Version 3) and MODIS Aqua (Version 5.1) for Dark Target (MYD-DT) and Deep Blue (MYD-DB) algorithms.

  11. Distribution of drifting seaweeds in eastern East China Sea

    NASA Astrophysics Data System (ADS)

    Komatsu, Teruhisa; Tatsukawa, Kenichi; Filippi, Jean B.; Sagawa, Tatsuyuki; Matsunaga, Daisuke; Mikami, Atsuko; Ishida, Kenichi; Ajisaka, Tetsuro; Tanaka, Katsuhiko; Aoki, Masakazu; Wang, Wei-Ding; Liu, Hui-Fei; Zhang, Shou-Du; Zhou, Min-Dong; Sugimoto, Takashige

    2007-09-01

    In offshore waters with relatively low primary production, drifting seaweeds composed of Sargassum species form an identical ecosystem such as an oasis in desert. Commercially important pelagic fishes such as jack mackerel ( Trachurus japonicus) and yellow tail ( Seriola quinqueradiata) spawn in East China Sea pass their juvenile period accompanying drifting seaweeds. Therefore drifting seaweeds are very important not only in offshore ecosystem but also fishery resources. However the distribution of drifting seaweeds in East China Sea has scarcely known. Then we conducted two research cruises of R/V Hakuho-Maru in May 2002 and in March 2004. During the cruises, drifting seaweeds were visually observed from the bridge and sampled with a towing net. The observation revealed that the drifting seaweeds were distributed along the front between the Kuroshio Current and coastal waters and mainly composed of one seaweed species, Sargassum horneri (Turner) C. Agardh from spring to early summer. There are no reports on geographical distribution of this species in the coasts south of southern Kyushu Island in Japan. Kuroshio Current flows northeastward there. Buoys with GPS attached to drifting seaweeds released off Zhejiang Province, China, in March 2005 to track their transport. Their positions monitored by ORBCOM satellite showed that they were transported to the area in East China Sea, where the drifting seaweeds were observed during the cruises, in 2 months. These facts suggest that S. horneri detached from Chinese coast in March or months earlier than March could be transported to fringe area of continental shelf and waters influenced by Kuroshio Current from March to May. Therefore the Sargassum forests, especially S. horneri, along the Chinese coast play a very important role in the ecosystem of the East China Sea as a source of drifting seaweeds.

  12. Global distribution of two fungal pathogens threatening endangered sea turtles.

    PubMed

    Sarmiento-Ramírez, Jullie M; Abella-Pérez, Elena; Phillott, Andrea D; Sim, Jolene; van West, Pieter; Martín, María P; Marco, Adolfo; Diéguez-Uribeondo, Javier

    2014-01-01

    Nascent fungal infections are currently considered as one of the main threats for biodiversity and ecosystem health, and have driven several animal species into critical risk of extinction. Sea turtles are one of the most endangered groups of animals and only seven species have survived to date. Here, we described two pathogenic species, i.e., Fusarium falciforme and Fusarium keratoplasticum, that are globally distributed in major turtle nesting areas for six sea turtle species and that are implicated in low hatch success. These two fungi possess key biological features that are similar to emerging pathogens leading to host extinction, e.g., high virulence, and a broad host range style of life. Their optimal growth temperature overlap with the optimal incubation temperature for eggs, and they are able to kill up to 90% of the embryos. Environmental forcing, e.g., tidal inundation and clay/silt content of nests, were correlated to disease development. Thus, these Fusarium species constitute a major threat to sea turtle nests, especially to those experiencing environmental stressors. These findings have serious implications for the survival of endangered sea turtle populations and the success of conservation programs worldwide. PMID:24465748

  13. Global distribution of two fungal pathogens threatening endangered sea turtles.

    PubMed

    Sarmiento-Ramírez, Jullie M; Abella-Pérez, Elena; Phillott, Andrea D; Sim, Jolene; van West, Pieter; Martín, María P; Marco, Adolfo; Diéguez-Uribeondo, Javier

    2014-01-01

    Nascent fungal infections are currently considered as one of the main threats for biodiversity and ecosystem health, and have driven several animal species into critical risk of extinction. Sea turtles are one of the most endangered groups of animals and only seven species have survived to date. Here, we described two pathogenic species, i.e., Fusarium falciforme and Fusarium keratoplasticum, that are globally distributed in major turtle nesting areas for six sea turtle species and that are implicated in low hatch success. These two fungi possess key biological features that are similar to emerging pathogens leading to host extinction, e.g., high virulence, and a broad host range style of life. Their optimal growth temperature overlap with the optimal incubation temperature for eggs, and they are able to kill up to 90% of the embryos. Environmental forcing, e.g., tidal inundation and clay/silt content of nests, were correlated to disease development. Thus, these Fusarium species constitute a major threat to sea turtle nests, especially to those experiencing environmental stressors. These findings have serious implications for the survival of endangered sea turtle populations and the success of conservation programs worldwide.

  14. Global Distribution of Two Fungal Pathogens Threatening Endangered Sea Turtles

    PubMed Central

    Sarmiento-Ramírez, Jullie M.; Abella-Pérez, Elena; Phillott, Andrea D.; Sim, Jolene; van West, Pieter; Martín, María P.; Marco, Adolfo; Diéguez-Uribeondo, Javier

    2014-01-01

    Nascent fungal infections are currently considered as one of the main threats for biodiversity and ecosystem health, and have driven several animal species into critical risk of extinction. Sea turtles are one of the most endangered groups of animals and only seven species have survived to date. Here, we described two pathogenic species, i.e., Fusarium falciforme and Fusarium keratoplasticum, that are globally distributed in major turtle nesting areas for six sea turtle species and that are implicated in low hatch success. These two fungi possess key biological features that are similar to emerging pathogens leading to host extinction, e.g., high virulence, and a broad host range style of life. Their optimal growth temperature overlap with the optimal incubation temperature for eggs, and they are able to kill up to 90% of the embryos. Environmental forcing, e.g., tidal inundation and clay/silt content of nests, were correlated to disease development. Thus, these Fusarium species constitute a major threat to sea turtle nests, especially to those experiencing environmental stressors. These findings have serious implications for the survival of endangered sea turtle populations and the success of conservation programs worldwide. PMID:24465748

  15. Water masses and 129I distribution in the Nordic Seas

    NASA Astrophysics Data System (ADS)

    Alfimov, Vasily; Aldahan, Ala; Possnert, Göran

    2013-01-01

    The application of the radioactive isotope iodine-129 as a tracer of water circulation in the oceans has provided interesting information with respect to sources and mixing of different water masses. We here present results of 129I distribution in water profiles located in the Nordic Seas and use the isotope to fingerprint water masses in the region. The samples were collected by the US research vessel Knorr in May-June 2002. 129I signatures along the Norwegian Sea reflect a mixing of 129I-rich surface water along the Scandinavian continental slope and 129I-poor North Atlantic surface water. These two water masses become less segregated along the Fram Strait where apparent 129I enrichment penetrates the return Arctic flow into the East Greenland Current. The 129I data further suggest existence of a water mass that is not entirely labeled with respect to origin at the Denmark Strait bottom water. This water parcel probably originates from the Iceland Sea. 129I data also shed light on the major deep water outflow from the Nordic Seas located at the Faeroe Bank Channel.

  16. Characterizing Aerosol Distributions and Optical Properties Using the NASA Langley High Spectral Resolution Lidar

    SciTech Connect

    Hostetler, Chris; Ferrare, Richard

    2013-02-14

    The objective of this project was to provide vertically and horizontally resolved data on aerosol optical properties to assess and ultimately improve how models represent these aerosol properties and their impacts on atmospheric radiation. The approach was to deploy the NASA Langley Airborne High Spectral Resolution Lidar (HSRL) and other synergistic remote sensors on DOE Atmospheric Science Research (ASR) sponsored airborne field campaigns and synergistic field campaigns sponsored by other agencies to remotely measure aerosol backscattering, extinction, and optical thickness profiles. Synergistic sensors included a nadir-viewing digital camera for context imagery, and, later in the project, the NASA Goddard Institute for Space Studies (GISS) Research Scanning Polarimeter (RSP). The information from the remote sensing instruments was used to map the horizontal and vertical distribution of aerosol properties and type. The retrieved lidar parameters include profiles of aerosol extinction, backscatter, depolarization, and optical depth. Products produced in subsequent analyses included aerosol mixed layer height, aerosol type, and the partition of aerosol optical depth by type. The lidar products provided vertical context for in situ and remote sensing measurements from other airborne and ground-based platforms employed in the field campaigns and was used to assess the predictions of transport models. Also, the measurements provide a data base for future evaluation of techniques to combine active (lidar) and passive (polarimeter) measurements in advanced retrieval schemes to remotely characterize aerosol microphysical properties. The project was initiated as a 3-year project starting 1 January 2005. It was later awarded continuation funding for another 3 years (i.e., through 31 December 2010) followed by a 1-year no-cost extension (through 31 December 2011). This project supported logistical and flight costs of the NASA sensors on a dedicated aircraft, the subsequent

  17. Longitudinal distributions of dicarboxylic acids, ω-oxoacids, pyruvic acid, α-dicarbonyls, and fatty acids in the marine aerosols from the central Pacific including equatorial upwelling

    NASA Astrophysics Data System (ADS)

    Hoque, Mir Md. Mozammal; Kawamura, Kimitaka

    2016-03-01

    Remote marine aerosol samples (total suspended particles) were collected during a cruise in the central Pacific from Japan to Mexico (1°59'N-35°N and 171°54'E-90°58'W). The aerosol samples were analyzed for dicarboxylic acids (C2-C11), ω-oxoacids, pyruvic acid, α-dicarbonyls, and fatty acids as well as organic and elemental carbon, water-soluble organic carbon, and total nitrogen (WSTN). During the study, diacids were the most abundant compound class followed by fatty acids, ω-oxoacids, and α-dicarbonyls. Molecular compositions of diacids showed a predominance of oxalic (C2) acid followed by malonic (C3) and succinic (C4) acids. Oxalic acid comprises 74% of total diacids. This result suggests that photochemical production of oxalic acid is significant over the central Pacific. Spatial distributions of diacids, ω-oxoacids, pyruvic acid, α-dicarbonyls, and fatty acids together with total carbon and WSTN showed higher abundances in the eastern equatorial Pacific where the upwelling of high-nutrient waters followed by high biological productivity is common, indicating that their in situ production is important in the warmer central Pacific through photochemical oxidation from their gaseous and particulate precursors. This study demonstrates that there is a strong linkage in biogeochemical cycles of carbon in the sea-air interface via ocean upwelling, phytoplankton productivity, sea-to-air emissions of organic matter, and formation of secondary organic aerosols in the eastern equatorial Pacific.

  18. Characterization of events by aerosol mass size distributions.

    PubMed

    Nicolás, José; Yubero, Eduardo; Galindo, Nuria; Giménez, Joaquín; Castañer, Ramón; Carratalá, Adoración; Crespo, Javier; Pastor, Carlos

    2009-02-01

    Continuous measurements of particle mass size distributions were carried out in summer 2004 at an urban location in the western Mediterranean using an optical particle counter. In this work we propose a simple methodology to identify PM episodes and determine their influence on mass size distributions. During the study period three types of event produced a significant increase in TSP daily levels: Saharan dust intrusions, firework displays and strong winds, modifying size distributions in different ways. As well, a traffic-related mass size spectrum was obtained showing road dust particles injected into the atmosphere by vehicle-induced resuspension having mainly aerodynamic diameters between 5 and 15 microm. This was confirmed by principal component and conditional probability function analyses.

  19. Sulphate aerosol size distributions at Mumbai, India, during the INDOEX-FFP (1998)

    NASA Astrophysics Data System (ADS)

    Venkataraman, Chandra; Sinha, Prashant; Bammi, Sachin

    Sulphate size distributions were measured at the coastal station of Mumbai (formerly Bombay) through 1998, during the Indian ocean experiment (INDOEX) first field phase (FFP), to fill current gaps in size-resolved aerosol chemical composition data. The paper examines meteorological, seasonal and source-contribution effects on sulphate aerosol and discusses potential effects of sulphate on regional climate. Sulphate size-distributions were largely trimodal with a condensation mode (mass median aerodynamic diameter or MMAD 0.6 μm), a droplet mode (MMAD 1.9-2.4 μm) and a coarse mode (MMAD 5 μm). Condensation mode sulphate mass-fractions were highest in winter, consistent with the high meteorological potential for gas-to-particle conversion along with low relative humidity (RH). The droplet mode concentrations and MMADs were larger in the pre-monsoon and winter than in monsoon, implying sulphate predominance in larger sized particles within this mode. In these seasons the high RH, and consequently greater aerosol water in the droplet mode, would favour aerosol-phase partitioning and reactions of SO 2. Coarse mode sulphate concentrations were lowest in the monsoon, when continental contribution to sulphate was low and washout was efficient. In winter and pre-monsoon, coarse mode sulphate concentrations were somewhat higher, likely from SO 2 gas-to-particle conversion. Low daytime sulphate concentrations with a large coarse fraction, along with largely onshore winds, indicated marine aerosol predominance. High nighttime sulphate concentrations and a coincident large fine fraction indicated contributions from anthropogenic/industrial sources or from gas-to-particle conversion. Monthly mean sulphate concentrations increased with increasing SO 2 concentrations, RH and easterly wind direction, indicating the importance of gas-to-particle conversion and industrial sources located to the east. Atmospheric chemistry effects on sulphate size distributions in Mumbai, indicated

  20. Macrophytobenthos of the Caspian Sea: Diversity, distribution, and productivity

    NASA Astrophysics Data System (ADS)

    Stepanian, O. V.

    2016-05-01

    In the Russian sector of the northern and middle Caspian Sea, 36 species of macroalgae have been identified. The green and red algae from the mesosaprobic group are dominant. An increase in the number of green algae species is revealed. The distribution of macroalgae is inhomogeneous. It is confined to the solid substrate and epiphyton. The biomass of seaweeds reaches 1.5 kg/m2. Climate change has little influence on the appearance of new species in the northern Caspian Sea, but new invaders can appear in the Middle and Southern Caspian. The distribution of aquatic and coastal hygrophytic vegetation shows considerable spatial dynamics due to fluctuations in the level and salinity of the Caspian Sea. The biomass of aquatic vegetation varies in a wide range from 0.5 to 10.0 kg/m2. Spatially detailed mathematical models adequately reflect the changes in key species of aquatic plants in space and time. It is shown that expansion of the zone of the seagrass Zostera noltii to shallow water areas is occurring at present, as well as shrinkage of the range of the dominant littoral aquatic plant Phragmites australis.

  1. Measuring the stratospheric aerosol size distribution profile following the next big volcanic eruption. What is required?

    NASA Astrophysics Data System (ADS)

    Deshler, T.

    2015-12-01

    Two of the key missing features of fresh and evolving volcanic plumes are the particle size distribution and its partitioning into non-volatile ash and volatile sulfate particles. Such information would allow more refined estimates of the evolution and dispersal of the aerosol, of the impacts of the aerosol on radiation and on stratospheric chemistry, and of the overall amount of sulfur injected into the stratosphere. To provide this information aerosol measurements must be sensitive to particles in the 0.1 - 10 μm radius range, with concentration detection thresholds > 0.001 cm-3, and to the total aerosol population. An added bonus would be a size resolved measurement of the non-volatile fraction of the aerosol. The measurements must span the lower and mid stratosphere up to about 30 km. There are no remote measurements which can provide this information. In situ measurements using aerosol and condensation nuclei counters are required. Aircraft platforms are available for measurements up to 20 km, but beyond that requires balloon platforms. Measurements above 20 km would be required for a large volcanic eruption. There are balloon-borne instruments capable of fulfilling all of the measurement requirements; however such instruments are reasonably large and not expendable. The difficulty is deploying the instruments, obtaining the flight permissions from air traffic control, and recovering the instruments after flight. Such difficulties are compounded in the tropics. This talk will detail some previous experience in this area and suggest ways forward to be ready for the next big eruption.

  2. Activity size distribution and residence time of 7Be aerosols in the Arctic atmosphere

    NASA Astrophysics Data System (ADS)

    Ioannidou, Alexandra; Paatero, Jussi

    2014-05-01

    The activity size distributions of the natural radionuclide tracer 7Be in different size range fractions (<0.39 μm, 0.39-0.69 μm, 0.69-1.3 μm, 1.3-2.1 μm, 2.1-4.2 μm, 4.2-10.2 μm and >10.2 μm) were determined in the boreal atmosphere in the Arctic Research Centre of the Finnish Meteorological Institute (FMI) at Sodankylä, Finland (67°22‧ N, 26°38‧ E, 180 m asl). The activity median aerodynamic diameter (AMAD) ranged from 0.54 μm to 1.05 μm (average 0.83 μm). A residence time of about 8 days applies to aerosols of 0.83 μm diameter, representing the residence of aerosol particles in arctic environment. The observed positive correlation between AMAD values and RH% can be explained by the fact that condensation during high relative humidity conditions becomes more intense, resulting in increased particle sizes of atmospheric aerosols. However, greater aerosol particle sizes means higher wet scavenging rate of aerosols and as a result lower activity concentration of 7Be in the atmosphere, explaining the anti-correlation between the AMAD values and activity concentrations of 7Be. But this associated with possibly higher scavenging rates of aerosols does not necessarily alone explain the anti-correlation between the AMAD and the 7Be activities. The air mass origin associated with synoptic scale weather phenomena may contribute to that too. The Flextra model was used to assess the transport pattern and to explain the deviation in radionuclide activity concentrations and AMAD values observed in the site of investigation.

  3. Meridional Distribution of Aerosol Optical Thickness over the Tropical Atlantic Ocean

    NASA Technical Reports Server (NTRS)

    Kishcha, P.; Silva, Arlindo M.; Starobinets, B.; Long, C. N.; Kalashnikova, O.; Alpert, P.

    2015-01-01

    Previous studies showed that, over the global ocean, there is hemispheric asymmetry in aerosols and no noticeable asymmetry in cloud fraction (CF). In the current study, we focus on the tropical Atlantic (30 Deg N 30 Deg S) which is characterized by significant amounts of Saharan dust dominating other aerosol species over the North Atlantic. We found that, by contrast to the global ocean, over a limited area such as the tropical Atlantic, strong meridional asymmetry in dust aerosols was accompanied by meridional CF asymmetry. During the 10-year study period (July 2002 June 2012), NASA Aerosol Reanalysis (aka MERRAero) showed that, when the meridional asymmetry in dust aerosol optical thickness (AOT) was the most pronounced (particularly in July), dust AOT averaged separately over the tropical North Atlantic was one order of magnitude higher than dust AOT averaged over the tropical South Atlantic. In the presence of such strong meridional asymmetry in dust AOT in July, CF averaged separately over the tropical North Atlantic exceeded CF averaged over the tropical South Atlantic by 20%. Our study showed significant cloud cover, up to 0.8 - 0.9, in July along the Saharan Air Layer which contributed to above-mentioned meridional CF asymmetry. Both Multi-Angle Imaging SpectroRadiometer (MISR) measurements and MERRAero data were in agreement on seasonal variations in meridional aerosol asymmetry. Meridional asymmetry in total AOT over the Atlantic was the most pronounced between March and July, when dust presence over the North Atlantic was maximal. In September and October, there was no noticeable meridional asymmetry in total AOT and meridional CF distribution over the tropical Atlantic was almost symmetrical.

  4. A statistical analysis of North East Atlantic (submicron) aerosol size distributions

    NASA Astrophysics Data System (ADS)

    Dall'Osto, M.; Monahan, C.; Greaney, R.; Beddows, D. C. S.; Harrison, R. M.; Ceburnis, D.; O'Dowd, C. D.

    2011-12-01

    The Global Atmospheric Watch research station at Mace Head (Ireland) offers the possibility to sample some of the cleanest air masses being imported into Europe as well as some of the most polluted being exported out of Europe. We present a statistical cluster analysis of the physical characteristics of aerosol size distributions in air ranging from the cleanest to the most polluted for the year 2008. Data coverage achieved was 75% throughout the year. By applying the Hartigan-Wong k-Means method, 12 clusters were identified as systematically occurring. These 12 clusters could be further combined into 4 categories with similar characteristics, namely: coastal nucleation category (occurring 21.3 % of the time), open ocean nucleation category (occurring 32.6% of the time), background clean marine category (occurring 26.1% of the time) and anthropogenic category (occurring 20% of the time) aerosol size distributions. The coastal nucleation category is characterised by a clear and dominant nucleation mode at sizes less than 10 nm while the open ocean nucleation category is characterised by a dominant Aitken mode between 15 nm and 50 nm. The background clean marine aerosol exhibited a clear bimodality in the sub-micron size distribution, with although it should be noted that either the Aitken mode or the accumulation mode may dominate the number concentration. However, peculiar background clean marine size distributions with coarser accumulation modes are also observed during winter months. By contrast, the continentally-influenced size distributions are generally more monomodal (accumulation), albeit with traces of bimodality. The open ocean category occurs more often during May, June and July, corresponding with the North East (NE) Atlantic high biological period. Combined with the relatively high percentage frequency of occurrence (32.6%), this suggests that the marine biota is an important source of new nano aerosol particles in NE Atlantic Air.

  5. Influence of marine aerosols and aerotechnogenic load on chemical composition of rainwaters on small islands (ludas) of the White Sea

    NASA Astrophysics Data System (ADS)

    Gorbacheva, Tamara; Mazukhina, Svetlana; Isaeva, Ludmila; Shumilov, Oleg

    2013-04-01

    In June 2001 intensive monitoring plots were established on the island part of Kandalaksha Bay of the White Sea (the island Tonnaya Luda; 67o06'60"N; 32o24'12"E) with the installation of stationary rainwater collectors. The purpose was studying the chemical composition of rain waters in the zone of cumulative influence of marine aerosols and aerotechnogenic load. Water sampling was carried out monthly during the vegetative season of 2001 and 2002. pH of rain water was determined by potentiometric method without preliminary filtration. The samples were passed through the paper filter with the pore diameter of 1-2.5 microns, the analysis of filtrate carried out by methods of atomic emission spectrometry (K, Na) and atomic absorption spectrometry (Ca, Mg, Zn, Mn, Cu, Ni, Al, Fe), total P and P of phosphates, Si and NH4+ - by photocolorimetry, total carbon - by bichromate method, NO3-, SO42-, Cl--by ion exchange chromatography method. Balance method was chosen as a research basis to determine the interrelation of rain water organic matter and dynamics of its redistribution under the influence of natural and technogenic factors. The difference between the cations sum (including NH4+and H+) and mineral acids anions sum (SO42-, Cl-, NO3-) was identified as organic acids anions concentration (μeq l-1). The level of Na, Cl-, K, Ca, Mg, SO42-, Sr in rainwaters on the island and the remote areas is indicative of the possible influence of marine aerosols on the island part of the White Sea. The increase of Al, Cu, Ni, Cd, Co concentrations in rainwaters up to one order against the background values points to the cumulative influence of the emissions of industrial enterprises located in the region. The relative stability of pH values of rain waters during all seasons indicates to the buffer action of weak organic acids anions. The correlation analysis of ionic structure in normal concentrations has allowed us to estimate the distribution of the cationic part from the

  6. Distributions of inorganic nutrients in the bohai sea of china

    NASA Astrophysics Data System (ADS)

    Zhengyan, Li; Jie, Bai; Jinhui, Shi; Huiwang, Gao

    2003-04-01

    To study the contents and distribution of inorganic nutrients in the Bohai Sea of China, two cruise surveys were undertaken in August (summer) 2000 and January (winter) 2001, respectively. A total of 595 water samples were collected from 91 stations and five nutrients, i.e., nitrate, nitrite, ammonia, phosphate and silicate, were analyzed for each sample. The results show that the average concentration of dissolved inorganic nitrogen (DIN) in the Bohai Sea in winter (6.529 μmol L-1) is significantly higher than that in summer (3.717 μmol L-1). The phosphorus concentration in winter (0.660 μmol L-1) is also significantly higher than that in summer (0.329 μmol L-1). Mean silicate concentration in winter (7.858 μmol L-1) is, however, not significantly different from that in summer (7.200 μmol L-1). Nutrients also vary considerably in different areas in Bohai Sea. DIN concentration in the Laizhou Bay (4.444 μmol L-1), for example, is significantly higher than those in the Bohai Bay (2.270 μmol L-1) and Bohai Strait (2.431 μmol L-1), which is caused by the discharge of large amounts of nitrogen into Laizhou Bay via Yellow River. The nutrients show different vertical distribution patterns. In summer, nutrients in bottom layer are generally richer than those in surface and middle layers. In winter, however, nutrients are not significantly different in different layers. Compared with historic data, DIN contents have increased continually since the early 1980 s. Based on atomic ratios of different nutrients, nitrogen is still the limiting factor for algal growth in the Bohai Sea.

  7. Global View of Aerosol Vertical Distributions from CALIPSO Lidar Measurements and GOCART Simulations: Regional and Seasonal Variations

    NASA Technical Reports Server (NTRS)

    Yu, Hongbin; Chin, Mian; Winker, David M.; Omar, Ali H.; Liu, Zhaoyan; Kittaka, Chieko; Diehl, Thomas

    2010-01-01

    This study examines seasonal variations of the vertical distribution of aerosols through a statistical analysis of the Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observations (CALIPSO) lidar observations from June 2006 to November 2007. A data-screening scheme is developed to attain good quality data in cloud-free conditions, and the polarization measurement is used to separate dust from non-dust aerosol. The CALIPSO aerosol observations are compared with aerosol simulations from the Goddard Chemistry Aerosol Radiation Transport (GOCART) model and aerosol optical depth (AOD) measurements from the MODerate resolution Imaging Spectroradiometer (MODIS). The CALIPSO observations of geographical patterns and seasonal variations of AOD are generally consistent with GOCART simulations and MODIS retrievals especially near source regions, while the magnitude of AOD shows large discrepancies in most regions. Both the CALIPSO observation and GOCART model show that the aerosol extinction scale heights in major dust and smoke source regions are generally higher than that in industrial pollution source regions. The CALIPSO aerosol lidar ratio also generally agrees with GOCART model within 30% on regional scales. Major differences between satellite observations and GOCART model are identified, including (1) an underestimate of aerosol extinction by GOCART over the Indian sub-continent, (2) much larger aerosol extinction calculated by GOCART than observed by CALIPSO in dust source regions, (3) much weaker in magnitude and more concentrated aerosol in the lower atmosphere in CALIPSO observation than GOCART model over transported areas in midlatitudes, and (4) consistently lower aerosol scale height by CALIPSO observation than GOCART model. Possible factors contributing to these differences are discussed.

  8. Anthropogenic aerosols and the distribution of past large‐scale precipitation change

    PubMed Central

    2015-01-01

    Abstract The climate response of precipitation to the effects of anthropogenic aerosols is a critical while not yet fully understood aspect in climate science. Results of selected models that participated the Coupled Model Intercomparison Project Phase 5 and the data from the Twentieth Century Reanalysis Project suggest that, throughout the tropics and also in the extratropical Northern Hemisphere, aerosols have largely dominated the distribution of precipitation changes in reference to the preindustrial era in the second half of the last century. Aerosol‐induced cooling has offset some of the warming caused by the greenhouse gases from the tropics to the Arctic and thus formed the gradients of surface temperature anomaly that enable the revealed precipitation change patterns to occur. Improved representation of aerosol‐cloud interaction has been demonstrated as the key factor for models to reproduce consistent distributions of past precipitation change with the reanalysis data. PMID:27134319

  9. Pharmacokinetics, tissue distribution, and the lactone/carboxylate equilibrium of hydroxycamptothecin delivered via aerosol in mice.

    PubMed

    Hu, Wei; Zhang, Chao; Hu, Wenjin; Fang, Yun; Hou, Wenjie

    2012-10-01

    Aerosol delivery is a route which is advantageous to the therapy of pulmonary diseases, such as lung cancer. The pharmacokinetics and tissue distribution after aerosol delivery of carboxylate form of hydroxycamptothecin (C-HCPT) were investigated. The concentrations of the three different types (lactone, carboxylate and the total of both forms) of HCPT were measured by HPLC analysis. The initial experiment showed no evident difference between lactone and carboxylate in the lungs during the aerosol treatment, compared with the HCPT content in plasma. The AUC(inf) value of lactone in the lungs was higher than that of carboxylate, which was 138,176.00 min ng g⁻¹ and 128,460.00 min ng g⁻¹, respectively. Meanwhile, AUC(inf) in the plasma during the entire treatment indicated that the lactone content was always at a lower level, and the carboxylate form tended to predominate, as shown by the lactone/carboxylate (L/C) equilibrium. The tissue distribution results showed that the lactone proportion in the liver increased up to the maximum value of 69.69% after aerosol administration, whereas the mean L/C equilibrium index for the liver was 2.07±1.06, and the C(max) and AUC(0-∞) values of the total HCPT were highest in the tissues. Based on these results we speculated that the initial wholly carboxylate form of the HCPT atomized liquid did not influence the transformation to lactone form. Moreover, the deposition of the total HCPT and lactone was higher in the lungs and other tissues than in the plasma after the aerosol treatment. This study will be beneficial to the therapy of pulmonary carcinoma. PMID:22858157

  10. Constraining Aerosol Optical Models Using Ground-Based, Collocated Particle Size and Mass Measurements in Variable Air Mass Regimes During the 7-SEAS/Dongsha Experiment

    NASA Technical Reports Server (NTRS)

    Bell, Shaun W.; Hansell, Richard A.; Chow, Judith C.; Tsay, Si-Chee; Wang, Sheng-Hsiang; Ji, Qiang; Li, Can; Watson, John G.; Khlystov, Andrey

    2012-01-01

    During the spring of 2010, NASA Goddard's COMMIT ground-based mobile laboratory was stationed on Dongsha Island off the southwest coast of Taiwan, in preparation for the upcoming 2012 7-SEAS field campaign. The measurement period offered a unique opportunity for conducting detailed investigations of the optical properties of aerosols associated with different air mass regimes including background maritime and those contaminated by anthropogenic air pollution and mineral dust. What appears to be the first time for this region, a shortwave optical closure experiment for both scattering and absorption was attempted over a 12-day period during which aerosols exhibited the most change. Constraints to the optical model included combined SMPS and APS number concentration data for a continuum of fine and coarse-mode particle sizes up to PM2.5. We also take advantage of an IMPROVE chemical sampler to help constrain aerosol composition and mass partitioning of key elemental species including sea-salt, particulate organic matter, soil, non sea-salt sulphate, nitrate, and elemental carbon. Our results demonstrate that the observed aerosol scattering and absorption for these diverse air masses are reasonably captured by the model, where peak aerosol events and transitions between key aerosols types are evident. Signatures of heavy polluted aerosol composed mostly of ammonium and non sea-salt sulphate mixed with some dust with transitions to background sea-salt conditions are apparent in the absorption data, which is particularly reassuring owing to the large variability in the imaginary component of the refractive indices. Extinctive features at significantly smaller time scales than the one-day sample period of IMPROVE are more difficult to reproduce, as this requires further knowledge concerning the source apportionment of major chemical components in the model. Consistency between the measured and modeled optical parameters serves as an important link for advancing remote

  11. Distribution of polyphenols and a surfactant component in skin during Aerosol OT microemulsion-enhanced intradermal delivery.

    PubMed

    Yutani, Reiko; Morita, Shin-ya; Teraoka, Reiko; Kitagawa, Shuji

    2012-01-01

    As for most other polyphenols, intradermal delivery of curcumin and resveratrol is limited; however, it was significantly improved by a microemulsion using Aerosol OT (Aerosol OT microemulsion) and Tween 80 (Tween 80 microemulsion) as surfactants. Aerosol OT microemulsion was more effective and the incorporation ratio of these polyphenols into skin by Aerosol OT microemulsion was five-fold or ten-fold that by Tween 80 microemulsion. To clarify the mechanism of the enhancement we examined the distribution of these polyphenols and the surfactant component, Aerosol OT, using excised guinea pig skin and Yucatan micropig (YMP) skin. During permeation, polyphenols distributed deep in the skin. In particular, a small molecule, resveratrol, was mainly present in the dermis in YMP skin. Aerosol OT also distributed deep in the skin. These findings suggest the possible involvement of the interaction of surfactant molecules with skin components in the enhanced delivery process of polyphenols. The distribution ratio between the dermis and epidermis of the polyphenols, including quercetin, in the presence of Aerosol OT microemulsion decreased with the increase of molecular weight in YMP skin, suggesting the possibility that distribution to the dermis is regulated by the molecular size.

  12. Investigating Chemical and Thermodynamic Conditions that Determine the Aerosol Inorganic Nitrate Size Distribution: Insights from Speciated PM2.5 and PM10 Hourly Datasets from an Urban Site

    NASA Astrophysics Data System (ADS)

    Griffith, S. M.; Huang, X. H. H.; Louie, P. K. K.; Yu, J. Z.

    2015-12-01

    Nitric acid (HNO3), the gas-phase precursor to aerosol nitrate is known to rapidly transfer to aerosols where NH4+ is in excess to SO42- present in the aerosol, but the HNO3 is also subject to the slower uptake onto sea salt and dust laden particles. Understanding the competition between these routes is necessary to predict the NO3- distribution and impact on aerosols. In this study, we investigated the conditions leading to predominant fine or coarse mode aerosol nitrate using an hourly MARGA 2S dataset from an urban site in Hong Kong. The hourly dataset of inorganic ions (SO42-, NH4+, NO3-, Na+, Cl-, Ca2+, K+, Mg2+) in 2 size ranges (fine, < 2.5 μm; fine+coarse, < 10 μm) and water-soluble gases (HNO3, HCl, and NH3) spanning more than 1 year provides a rich trove for analyzing aerosol nitrate chemistry and the underlying mechanisms that ultimately determine the fraction of NO3- in the fine mode. The urban site in this study is initially characterized for seasonal environmental conditions and the aerosol chemical composition. The relationship between excess NH4+ and NO3- in the fine mode is detailed and contrasted with the influence on fine mode NO3- from uptake on sea salt and dust, which is typically relegated as a 'coarse-mode' mechanism. The distribution of NO3- in the fine and coarse modes is compared with the distribution of the other inorganic ions, where sea-salt ion (Na+, Mg2+) distributions yield the highest explained variability for the nitrate distributions. As a complement to that finding, the cation equivalency (excluding NH4+) in the coarse mode proves to be a crucial factor in leveraging the distribution away from fine mode nitrate. The uptake potential of the water-soluble gases is used to drive a mass transfer model and compare with thermodynamic equilibrium results. In the modeling, the partitioning cycles of fine and coarse mode aerosol nitrate highlight the dynamic relationship between NO3- and Cl- in both the fine and coarse modes, where the

  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. Asian aerosols: current and year 2030 distributions and implications to human health and regional climate change.

    PubMed

    Carmichael, Gregory R; Adhikary, Bhupesh; Kulkarni, Sarika; D'Allura, Alessio; Tang, Youhua; Streets, David; Zhang, Qiang; Bond, Tami C; Ramanathan, Veerabhadran; Jamroensan, Aditsuda; Marrapu, Pallavi

    2009-08-01

    Aerosol distributions in Asia calculated over a 4-year period and constrained by satellite observations of aerosol optical depth (AOD) are presented. Vast regions in Asia that include > 80% of the population have PM2.5 concentrations that exceed on an annual basis the WHO guideline of 10 microg/m3, often by factors of 2 to 4. These high aerosol loadings also have important radiative effects, causing a significant dimming at the surface, and mask approximately 45% of the warming by greenhouse gases. Black carbon (BC) concentrations are high throughout Asia, representing 5-10% of the total AOD, and contributing significantly to atmospheric warming (its warming potential is approximately 55% of that due to CO2). PM levels and AODs in year 2030, estimated based on simulations that consider future changes in emissions, are used to explore opportunities for win-win strategies built upon addressing air quality and climate change together. It is found that in 2030 the PM2.5 levels in significant parts of Asia will increase and exacerbate health impacts; but the aerosols will have a larger masking effect on radiative forcing, due to a decrease in BC and an increase in SO2 emissions.

  15. Aerosol mobility imaging for rapid size distribution measurements

    DOEpatents

    Wang, Jian; Hering, Susanne Vera; Spielman, Steven Russel; Kuang, Chongai

    2016-07-19

    A parallel plate dimensional electrical mobility separator and laminar flow water condensation provide rapid, mobility-based particle sizing at concentrations typical of the remote atmosphere. Particles are separated spatially within the electrical mobility separator, enlarged through water condensation, and imaged onto a CCD array. The mobility separation distributes particles in accordance with their size. The condensation enlarges size-separated particles by water condensation while they are still within the gap of the mobility drift tube. Once enlarged the particles are illuminated by a laser. At a pre-selected frequency, typically 10 Hz, the position of all of the individual particles illuminated by the laser are captured by CCD camera. This instantly records the particle number concentration at each position. Because the position is directly related to the particle size (or mobility), the particle size spectra is derived from the images recorded by the CCD.

  16. Aged boreal biomass-burning aerosol size distributions from BORTAS 2011

    NASA Astrophysics Data System (ADS)

    Sakamoto, K. M.; Allan, J. D.; Coe, H.; Taylor, J. W.; Duck, T. J.; Pierce, J. R.

    2015-02-01

    Biomass-burning aerosols contribute to aerosol radiative forcing on the climate system. The magnitude of this effect is partially determined by aerosol size distributions, which are functions of source fire characteristics (e.g. fuel type, MCE) and in-plume microphysical processing. The uncertainties in biomass-burning emission number-size distributions in climate model inventories lead to uncertainties in the CCN (cloud condensation nuclei) concentrations and forcing estimates derived from these models. The BORTAS-B (Quantifying the impact of BOReal forest fires on Tropospheric oxidants over the Atlantic using Aircraft and Satellite) measurement campaign was designed to sample boreal biomass-burning outflow over eastern Canada in the summer of 2011. Using these BORTAS-B data, we implement plume criteria to isolate the characteristic size distribution of aged biomass-burning emissions (aged ~ 1-2 days) from boreal wildfires in northwestern Ontario. The composite median size distribution yields a single dominant accumulation mode with Dpm = 230 nm (number-median diameter) and σ = 1.5, which are comparable to literature values of other aged plumes of a similar type. The organic aerosol enhancement ratios (ΔOA / ΔCO) along the path of Flight b622 show values of 0.09-0.17 μg m-3 ppbv-1 (parts per billion by volume) with no significant trend with distance from the source. This lack of enhancement ratio increase/decrease with distance suggests no detectable net OA (organic aerosol) production/evaporation within the aged plume over the sampling period (plume age: 1-2 days), though it does not preclude OA production/loss at earlier stages. A Lagrangian microphysical model was used to determine an estimate of the freshly emitted size distribution corresponding to the BORTAS-B aged size distributions. The model was restricted to coagulation and dilution processes based on the insignificant net OA production/evaporation derived from the ΔOA / ΔCO enhancement ratios. We

  17. Breaking waves and near-surface sea spray aerosol dependence on changing winds: Wave breaking efficiency and bubble-related air-sea interaction processes

    NASA Astrophysics Data System (ADS)

    Hwang, P. A.; Savelyev, I. B.; Anguelova, M. D.

    2016-05-01

    Simultaneous measurements of sea spray aerosol (SSA), wind, wave, and microwave brightness temperature are obtained in the open ocean on-board Floating Instrument Platform (FLIP). These data are analysed to clarify the ocean surface processes important to SSA production. Parameters are formulated to represent surface processes with characteristic length scales spanning a broad range. The investigation reveals distinct differences of the SSA properties in rising winds and falling winds, with higher SSA volume in falling winds. Also, in closely related measurements of whitecap coverage, higher whitecap fraction as a function of wind speed is found in falling winds than in rising winds or in older seas than in younger seas. Similar trend is found in the short scale roughness reflected in the microwave brightness temperature data. In the research of length and velocity scales of breaking waves, it has been observed that the length scale of wave breaking is shorter in mixed seas than in wind seas. For example, source function analysis of short surface waves shows that the characteristic length scale of the dissipation function shifts toward higher wavenumber (shorter wavelength) in mixed seas than in wind seas. Similarly, results from feature tracking or Doppler analysis of microwave radar sea spikes, which are closely associated with breaking waves, show that the magnitude of the average breaking wave velocity is smaller in mixed seas than in wind seas. Furthermore, breaking waves are observed to possess geometric similarity. Applying the results of breaking wave analyses to the SSA and whitecap observations described above, it is suggestive that larger air cavities resulting from the longer breakers are entrained in rising high winds. The larger air cavities escape rapidly due to buoyancy before they can be fully broken down into small bubbles for the subsequent SSA production or whitecap manifestation. In contrast, in falling winds (with mixed seas more likely), the

  18. Global Aerosols

    Atmospheric Science Data Center

    2013-04-19

    ... sizes and from multiple sources, including biomass burning, mineral dust, sea salt and regional industrial pollution. A color scale is ... desert source region. Deserts are the main sources of mineral dust, and MISR obtains aerosol optical depth at visible wavelengths ...

  19. Sugars in Antarctic aerosol

    NASA Astrophysics Data System (ADS)

    Barbaro, Elena; Kirchgeorg, Torben; Zangrando, Roberta; Vecchiato, Marco; Piazza, Rossano; Barbante, Carlo; Gambaro, Andrea

    2015-10-01

    The processes and transformations occurring in the Antarctic aerosol during atmospheric transport were described using selected sugars as source tracers. Monosaccharides (arabinose, fructose, galactose, glucose, mannose, ribose, xylose), disaccharides (sucrose, lactose, maltose, lactulose), alcohol-sugars (erythritol, mannitol, ribitol, sorbitol, xylitol, maltitol, galactitol) and anhydrosugars (levoglucosan, mannosan and galactosan) were measured in the Antarctic aerosol collected during four different sampling campaigns. For quantification, a sensitive high-pressure anion exchange chromatography was coupled with a single quadrupole mass spectrometer. The method was validated, showing good accuracy and low method quantification limits. This study describes the first determination of sugars in the Antarctic aerosol. The total mean concentration of sugars in the aerosol collected at the "Mario Zucchelli" coastal station was 140 pg m-3; as for the aerosol collected over the Antarctic plateau during two consecutive sampling campaigns, the concentration amounted to 440 and 438 pg m-3. The study of particle-size distribution allowed us to identify the natural emission from spores or from sea-spray as the main sources of sugars in the coastal area. The enrichment of sugars in the fine fraction of the aerosol collected on the Antarctic plateau is due to the degradation of particles during long-range atmospheric transport. The composition of sugars in the coarse fraction was also investigated in the aerosol collected during the oceanographic cruise.

  20. Tropospheric Aerosols

    NASA Astrophysics Data System (ADS)

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

    2003-12-01

    It is widely believed that "On a clear day you can see forever," as proclaimed in the 1965 Broadway musical of the same name. While an admittedly beautiful thought, we all know that this concept is only figurative. Aside from Earth's curvature and Rayleigh scattering by air molecules, aerosols - colloidal suspensions of solid or liquid particles in a gas - limit our vision. Even on the clearest day, there are billions of aerosol particles per cubic meter of air.Atmospheric aerosols are commonly referred to as smoke, dust, haze, and smog, terms that are loosely reflective of their origin and composition. Aerosol particles have arisen naturally for eons from sea spray, volcanic emissions, wind entrainment of mineral dust, wildfires, and gas-to-particle conversion of hydrocarbons from plants and dimethylsulfide from the oceans. However, over the industrial period, the natural background aerosol has been greatly augmented by anthropogenic contributions, i.e., those produced by human activities. One manifestation of this impact is reduced visibility (Figure 1). Thus, perhaps more than in other realms of geochemistry, when considering the composition of the troposphere one must consider the effects of these activities. The atmosphere has become a reservoir for vast quantities of anthropogenic emissions that exert important perturbations on it and on the planetary ecosystem in general. Consequently, much recent research focuses on the effects of human activities on the atmosphere and, through them, on the environment and Earth's climate. For these reasons consideration of the geochemistry of the atmosphere, and of atmospheric aerosols in particular, must include the effects of human activities. (201K)Figure 1. Impairment of visibility by aerosols. Photographs at Yosemite National Park, California, USA. (a) Low aerosol concentration (particulate matter of aerodynamic diameter less than 2.5 μm, PM2.5=0.3 μg m-3; particulate matter of aerodynamic diameter less than 10

  1. Distribution and assessment of marine debris in the deep Tyrrhenian Sea (NW Mediterranean Sea, Italy).

    PubMed

    Angiolillo, Michela; di Lorenzo, Bianca; Farcomeni, Alessio; Bo, Marzia; Bavestrello, Giorgio; Santangelo, Giovanni; Cau, Angelo; Mastascusa, Vincenza; Cau, Alessandro; Sacco, Flavio; Canese, Simonepietro

    2015-03-15

    Marine debris is a recognized global ecological concern. Little is known about the extent of the problem in the Mediterranean Sea regarding litter distribution and its influence on deep rocky habitats. A quantitative assessment of debris present in the deep seafloor (30-300 m depth) was carried out in 26 areas off the coast of three Italian regions in the Tyrrhenian Sea, using a Remotely Operated Vehicle (ROV). The dominant type of debris (89%) was represented by fishing gears, mainly lines, while plastic objects were recorded only occasionally. Abundant quantities of gears were found on rocky banks in Sicily and Campania (0.09-0.12 debris m(-2)), proving intense fishing activity. Fifty-four percent of the recorded debris directly impacted benthic organisms, primarily gorgonians, followed by black corals and sponges. This work provides a first insight on the impact of marine debris in Mediterranean deep ecosystems and a valuable baseline for future comparisons. PMID:25604749

  2. Distribution and assessment of marine debris in the deep Tyrrhenian Sea (NW Mediterranean Sea, Italy).

    PubMed

    Angiolillo, Michela; di Lorenzo, Bianca; Farcomeni, Alessio; Bo, Marzia; Bavestrello, Giorgio; Santangelo, Giovanni; Cau, Angelo; Mastascusa, Vincenza; Cau, Alessandro; Sacco, Flavio; Canese, Simonepietro

    2015-03-15

    Marine debris is a recognized global ecological concern. Little is known about the extent of the problem in the Mediterranean Sea regarding litter distribution and its influence on deep rocky habitats. A quantitative assessment of debris present in the deep seafloor (30-300 m depth) was carried out in 26 areas off the coast of three Italian regions in the Tyrrhenian Sea, using a Remotely Operated Vehicle (ROV). The dominant type of debris (89%) was represented by fishing gears, mainly lines, while plastic objects were recorded only occasionally. Abundant quantities of gears were found on rocky banks in Sicily and Campania (0.09-0.12 debris m(-2)), proving intense fishing activity. Fifty-four percent of the recorded debris directly impacted benthic organisms, primarily gorgonians, followed by black corals and sponges. This work provides a first insight on the impact of marine debris in Mediterranean deep ecosystems and a valuable baseline for future comparisons.

  3. [Geochemical distribution of dissolved bismuth in the Yellow Sea and East China Sea].

    PubMed

    Wu, Xiao-Dan; Song, Jin-Ming; Wu, Bin; Li, Xue-Gang

    2014-01-01

    Occurrence level, geochemical distribution of dissolved bismuth and its coupling relationship to eco-environment were investigated in the Yellow Sea and East China Sea to explore the source and influencing factors. The results showed that the concentration of dissolved bismuth was within the range of 0-0. 029 microg x L(-1) at the surface and 0.001-0.189 microg x L(-1) at the bottom, with the averages of 0.008 and 0.016 microg x L(-1), respectively. Horizontally, low value of dissolved bismuth exhibited the bidirectional extension feature, indicating that it could trace the path of Changjiang Diluted Water. High value of dissolved bismuth was observed where the Subei Costal Current and Yellow Sea Warm Current flowed and the Changjiang Diluted Water and Zhejiang-Fujian Coastal Current met, suggesting that it was controlled by the cycle of current system. Vertically, the coastal water was fully mixed by water convection and eddy mixing, and was divided from the stratified water by strong tidal front, which blocked the transport of dissolved bismuth to the open sea. Thus, the concentration in front area was significantly higher than that in the open sea. Diurnal variation of dissolved bismuth was related to the hydrodynamic conditions (tide, suspension and thermocline) instead of the environmental factors (temperature and salinity). Positive relationship to SPM (suspended particulate matter) clarified that bismuth was prone to release from solid phase to liquid phase. Furthermore, conditions with temperature ranging 22-27 degrees C, salinity ranging 28-31 and pH ranging 7.9-8.1 were shown to be optimal for the release process.

  4. 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...

  5. A Physically Based Framework for Modelling the Organic Fractionation of Sea Spray Aerosol from Bubble Film Langmuir Equilibria

    SciTech Connect

    Burrows, Susannah M.; Ogunro, O.; Frossard, Amanda; Russell, Lynn M.; Rasch, Philip J.; Elliott, S.

    2014-12-19

    The presence of a large fraction of organic matter in primary sea spray aerosol (SSA) can strongly affect its cloud condensation nuclei activity and interactions with marine clouds. Global climate models require new parameterizations of the SSA composition in order to improve the representation of these processes. Existing proposals for such a parameterization use remotely-sensed chlorophyll-a concentrations as a proxy for the biogenic contribution to the aerosol. However, both observations and theoretical considerations suggest that existing relationships with chlorophyll-a, derived from observations at only a few locations, may not be representative for all ocean regions. We introduce a novel framework for parameterizing the fractionation of marine organic matter into SSA based on a competitive Langmuir adsorption equilibrium at bubble surfaces. Marine organic matter is partitioned into classes with differing molecular weights, surface excesses, and Langmuir adsorption parameters. The classes include a lipid-like mixture associated with labile dissolved organic carbon (DOC), a polysaccharide-like mixture associated primarily with semi-labile DOC, a protein-like mixture with concentrations intermediate between lipids and polysaccharides, a processed mixture associated with recalcitrant surface DOC, and a deep abyssal humic-like mixture. Box model calculations have been performed for several cases of organic adsorption to illustrate the underlying concepts. We then apply the framework to output from a global marine biogeochemistry model, by partitioning total dissolved organic carbon into several classes of macromolecule. Each class is represented by model compounds with physical and chemical properties based on existing laboratory data. This allows us to globally map the predicted organic mass fraction of the nascent submicron sea spray aerosol. Predicted relationships between chlorophyll-\\textit{a} and organic fraction are similar to existing empirical

  6. Movements and distribution of polar bears in the Beaufort sea

    USGS Publications Warehouse

    Amstrup, Steven C.; Durner, G.M.; Stirling, I.; Lunn, N.J.; Messier, F.

    2000-01-01

    We fitted 173 satellite radio collars (platform transmitter terminals) to 121 adult female polar bears in the Beaufort Sea and relocated the bears 44 736 times between 1985 and 1995. We regularly resighted many instrumented bears so that we could ascertain whether changes in movements or distribution were related to reproductive status. Mean short-term movement rates were less than 2 km/h for all classes of bears. Maximum movement rates occurred in winter and early summer. In the southern Beaufort Sea (SBS), net geographic movements from the beginning to the end of each month were smaller for females with cubs of the year than for solitary females, and larger in November than in April, May, or July. In May, June, July, and August, radio-collared bears in the SBS moved north. They moved south in October. In the northern Beaufort Sea (NBS), bears moved north in June and south in March and September. Total annual movements ranged from 1406 to 6203 km. Mean total distances moved each month ranged from 79 to 420 km. Total monthly movements by SBS bears were largest in early winter and smallest in early spring. In the NBS, movements were largest in summer and smallest in winter. In the SBS, females with cubs moved less each month than other females. Annual activity areas ranged from 7264 to 596 800 km2. Monthly activity areas ranged from 88 to 9760 km2. Seasonal fidelity to activity areas of bears captured in all parts of the Beaufort Sea was strongest in summer and weakest in spring.

  7. Seasonal variation of vertical distribution of aerosol single scattering albedo over Indian sub-continent: RAWEX aircraft observations

    NASA Astrophysics Data System (ADS)

    Suresh Babu, S.; Nair, Vijayakumar S.; Gogoi, Mukunda M.; Krishna Moorthy, K.

    2016-01-01

    To characterize the vertical distribution of aerosols and its seasonality (especially the single scattering albedo, SSA) extensive profiling of aerosol scattering and absorption coefficients have been carried out using an instrumented aircraft from seven base stations spread across the Indian mainland during winter 2012 and spring/pre-monsoon 2013 under the Regional Aerosol Warming Experiment (RAWEX). Spatial variation of the vertical profiles of the asymmetry parameter, the wavelength exponent of the absorption coefficient and the single scattering albedo, derived from the measurements, are used to infer the source characteristics of winter and pre-monsoon aerosols as well as the seasonality of free tropospheric aerosols. The relatively high value of the wavelength exponent of absorption coefficient over most of the regions indicates the contribution from biomass burning and dust aerosols up to lower free tropospheric altitudes. A clear enhancement in aerosol loading and its absorbing nature is seen at lower free troposphere levels (above the planetary boundary layer) over the entire mainland during spring/pre-monsoon season compared to winter, whereas concentration of aerosols within the boundary layer showed a decrease from winter to spring. This could have significant implications on the aerosol heating structure over the Indian region and hence the regional climate.

  8. Modeling radium distribution in coastal aquifers during sea level changes: The Dead Sea case

    USGS Publications Warehouse

    Kiro, Yael; Yechieli, Yoseph; Voss, Clifford I.; Starinsky, Abraham; Weinstein, Yishai

    2012-01-01

    We present a new approach to studying the behavior of radium isotopes in a coastal aquifer. In order to simulate radium isotope distributions in the dynamic flow field of the Dead Sea aquifer, a multi-species density dependent flow model (SUTRA-MS) was used. Field data show that the activity of 226Ra decreases from 140 to 60 dpm/L upon entering the aquifer from the Dead Sea, and then further decreases linearly due to mixing with Ra-poor fresh water. On the other hand, an increase is observed in the activity of the shorter-lived isotopes (up to 52 dpm/L 224Ra and 31 dpm/L 223Ra), which are relatively low in Dead Sea water (up to 2.5 dpm/L 224Ra and 0.5 dpm/L 223Ra). The activities of the short lived radium isotopes also decrease with decreasing salinity, which is due to the effect of salinity on the adsorption of radium. The relationship between 224Ra and salinity suggests that the adsorption partition coefficient (K) is linearly related to salinity. Simulations of the steady-state conditions, show that the distance where equilibrium activity is attained for each radium isotope is affected by the isotope half-life, K and the groundwater velocity, resulting in a longer distance for the long-lived radium isotopes. K affects the radium distribution in transient conditions, especially that of the long-lived radium isotopes. The transient conditions in the Dead Sea system, with a 1 m/yr lake level drop, together with the radium field data, constrains K to be relatively low (226Ra cannot be explained by adsorption, and it is better explained by removal via coprecipitation, probably with barite or celestine.

  9. Modeling radium distribution in coastal aquifers during sea level changes: The Dead Sea case

    NASA Astrophysics Data System (ADS)

    Kiro, Yael; Yechieli, Yoseph; Voss, Clifford I.; Starinsky, Abraham; Weinstein, Yishai

    2012-07-01

    We present a new approach to studying the behavior of radium isotopes in a coastal aquifer. In order to simulate radium isotope distributions in the dynamic flow field of the Dead Sea aquifer, a multi-species density dependent flow model (SUTRA-MS) was used. Field data show that the activity of 226Ra decreases from 140 to 60 dpm/L upon entering the aquifer from the Dead Sea, and then further decreases linearly due to mixing with Ra-poor fresh water. On the other hand, an increase is observed in the activity of the shorter-lived isotopes (up to 52 dpm/L 224Ra and 31 dpm/L 223Ra), which are relatively low in Dead Sea water (up to 2.5 dpm/L 224Ra and 0.5 dpm/L 223Ra). The activities of the short lived radium isotopes also decrease with decreasing salinity, which is due to the effect of salinity on the adsorption of radium. The relationship between 224Ra and salinity suggests that the adsorption partition coefficient (K) is linearly related to salinity. Simulations of the steady-state conditions, show that the distance where equilibrium activity is attained for each radium isotope is affected by the isotope half-life, K and the groundwater velocity, resulting in a longer distance for the long-lived radium isotopes. K affects the radium distribution in transient conditions, especially that of the long-lived radium isotopes. The transient conditions in the Dead Sea system, with a 1 m/yr lake level drop, together with the radium field data, constrains K to be relatively low (<10). Thus, the sharp decrease in 226Ra cannot be explained by adsorption, and it is better explained by removal via coprecipitation, probably with barite or celestine.

  10. Determination of particle nucleation and growth rates from measured aerosol size distributions

    NASA Astrophysics Data System (ADS)

    Verheggen, B.; Mozurkewich, M.

    2003-04-01

    The effects of aerosols on atmospheric chemistry, health and climate are dependent on particle size and composition, and therefore on particle nucleation and growth. An analytical model has been developed to determine nucleation and growth rates from measurements of consecutive aerosol size distributions. The evolution of an aerosol population in time is described by the General Dynamic Equation (GDE). Wall loss, coagulation loss and coagulation production are determined, based on the measured aerosol size distributions. Taking their contributions into account, a non-linear regression analysis of the GDE is performed for each time interval to find the value of the growth rate, that gives best agreement between the measured and calculated change in the size distribution. Other parameters can also be verified and/or optimized by regression analysis. Knowing the growth rate as a function of time (and size) from the regression analysis, each measured cohort of particles is tracked backwards in time to their time of formation, where the radius of the critical cluster is assumed to be 0.5 nm. The number density of each cohort has decreased since their formation, due to wall losses and coagulation processes. Perturbation theory is used to approximate the contribution of within mode coagulation in decreasing the number density. Wall losses and coagulation scavenging are well characterized for each time interval. The integrated losses, from time of formation to time of measurement, are used to obtain the number of nucleated particles, and ultimately the -empirically determined- nucleation rate. The analysis is applied to measurements made in Calspan's 590 m3 smog chamber, following SO2 nucleation.

  11. Premonsoon shortwave aerosol radiative forcings over the Arabian Sea and tropical Indian Ocean: Yearly and monthly mean variabilities

    NASA Astrophysics Data System (ADS)

    Ramachandran, S.

    2005-04-01

    The yearly and monthly mean variations in the clear-sky shortwave aerosol direct radiative forcings are estimated over Coastal India (CI), the Arabian Sea (AS), and tropical Indian Ocean (TIO) during winter monsoon seasons of 1996-2000. The 5-year mean TOA forcings are estimated to be -10, -9, and -4 W m-2 over CI, AS, and TIO. Surface (SFC) forcings are estimated to be -29, -22, and -5 W m-2 over CI, AS, and TIO, respectively. Atmosphere absorptions are quite large over CI and AS at +19 and +13 W m-2, indicating a significant influence of soot emitted from fossil fuel, biomass burning, and mineral dust. The yearly and monthly mean aerosol forcings are found to exhibit variations. The large atmospheric absorption estimated over CI and AS is found to be a feature of the other polluted ocean and land regions. The influence of relative humidity on the aerosol forcing is estimated. It is shown that as the single scattering albedo increases, the TOA forcing increases while the SFC forcing decreases. With an increase in aerosol optical depths the forcings at TOA and SFC are found to increase substantially, while an increase in the asymmetry parameter is found to decrease both TOA and SFC forcings. The effective factors (forcing at 80% RH/forcing at 30% RH) for the surface are found to be about 1.2 over CI, AS, and 1.4 over TIO. The effective factors estimated over these oceanic regions are found to be smaller than those obtained over the southeastern United States and the mid-Atlantic coast, indicating that the composition of aerosols found over these regions is different.

  12. Effect of particle size of bronchodilator aerosols on lung distribution and pulmonary function in patients with chronic asthma.

    PubMed

    Mitchell, D M; Solomon, M A; Tolfree, S E; Short, M; Spiro, S G

    1987-06-01

    The particle size of bronchodilator aerosols may be important in determining the site of deposition in the lung and their therapeutic effect. The distribution of aerosols (labelled with technetium-99m diethylene triamine pentacetic acid) of two different particle sizes has been studied by gamma camera imaging. The particles had mass median aerodynamic diameters (geometric standard deviations) of 1.4 (1.4) and 5.5 (2.3) micron, and they were administered from a jet nebuliser to eight patients with chronic severe stable asthma. There was no significant difference in peripheral lung deposition with the two aerosols in any patient. The bronchodilator effect of the two aerosols was determined from cumulative dose-response studies. To avoid large doses that might mask possible differences in effect due to aerosol size, small, precisely determined incremental amounts of salbutamol (25-250 micrograms total lung dose) were used. The two doses were given via a nebuliser on separate occasions and the bronchodilator response was measured from FEV1, forced vital capacity, and peak expiratory flow 30 minutes after each dose. Bronchodilatation was similar with the two aerosols at each dose of salbutamol. There was therefore no difference in distribution within the lung or any difference in bronchodilator effect between an aerosol of small (1.4 micron) particle size and an aerosol of 5.5 microns in patients with severe but stable asthma. PMID:3660305

  13. A 4-D climatology (1979-2009) of the monthly tropospheric aerosol optical depth distribution over the Mediterranean region from a comparative evaluation and blending of remote sensing and model products

    NASA Astrophysics Data System (ADS)

    Nabat, P.; Somot, S.; Mallet, M.; Chiapello, I.; Morcrette, J. J.; Solmon, F.; Szopa, S.; Dulac, F.; Collins, W.; Ghan, S.; Horowitz, L. W.; Lamarque, J. F.; Lee, Y. H.; Naik, V.; Nagashima, T.; Shindell, D.; Skeie, R.

    2013-05-01

    Since the 1980s several spaceborne sensors have been used to retrieve the aerosol optical depth (AOD) over the Mediterranean region. In parallel, AOD climatologies coming from different numerical model simulations are now also available, permitting to distinguish the contribution of several aerosol types to the total AOD. In this work, we perform a comparative analysis of this unique multi-year database in terms of total AOD and of its apportionment by the five main aerosol types (soil dust, sea-salt, sulfate, black and organic carbon). We use 9 different satellite-derived monthly AOD products: NOAA/AVHRR, SeaWiFS (2 products), TERRA/MISR, TERRA/MODIS, AQUA/MODIS, ENVISAT/MERIS, PARASOL/POLDER and MSG/SEVIRI, as well as 3 more historical datasets: NIMBUS7/CZCS, TOMS (onboard NIMBUS7 and Earth-Probe) and METEOSAT/MVIRI. Monthly model datasets include the aerosol climatology from Tegen et al. (1997), the climate-chemistry models LMDz-OR-INCA and RegCM-4, the multi-model mean coming from the ACCMIP exercise, and the reanalyses GEMS and MACC. Ground-based Level-2 AERONET AOD observations from 47 stations around the basin are used here to evaluate the model and satellite data. The sensor MODIS (on AQUA and TERRA) has the best average AOD scores over this region, showing a relevant spatio-temporal variability and highlighting high dust loads over Northern Africa and the sea (spring and summer), and sulfate aerosols over continental Europe (summer). The comparison also shows limitations of certain datasets (especially MERIS and SeaWiFS standard products). Models reproduce the main patterns of the AOD variability over the basin. The MACC reanalysis is the closest to AERONET data, but appears to underestimate dust over Northern Africa, where RegCM-4 is found closer to MODIS thanks to its interactive scheme for dust emissions. The vertical dimension is also investigated using the CALIOP instrument. This study confirms differences of vertical distribution between dust

  14. Investigating primary marine aerosol properties: CCN activity of sea salt and mixed particles

    NASA Astrophysics Data System (ADS)

    King, S. M.; Butcher, A. C.; Rosenoern, T.; Coz, E.; Lieke, K. I.; de Leeuw, G.; Nilsson, E. D.; Bilde, M.

    2012-04-01

    Sea salt particles ejected as a result of bubbles bursting from artificial seawater in a closed stainless steel tank were sampled for size distribution, morphology, and cloud condensation nucleus (CCN) activity. The two-component artificial seawater consisted of salt, either NaCl or sea salt, and one organic compound in deionized water. Several organic molecules representative of oceanic organic matter were investigated. Bubbles were generated either by aeration through a porous diffuser or by water jet impingement on the surface of the artificial seawater. The effect of bubble lifetime, which was controlled by varying the depth of the diffuser in the water column, on particle size and CCN activity was investigated and was found to be insignificant for the organic compounds studied. The CCN activities of particles produced from diffuser-generated bubbles were generally governed by the high hygroscopicity of salt, such that activation was indistinguishable from that of salt, except in the case of very low mass ratio of salt to organic matter in the seawater solution. There was, however, a considerable decrease in CCN activity for particles produced from jet impingement on seawater that had a salinity of 10‰ and contained 0.45 mM of sodium laurate, an organic surfactant. The production of a thick foam layer from impingement may explain the difference in activation and supports hypotheses that particle production from the two methods of generating bubbles is not similar. Accurate conclusions from observed CCN activities of particles from artificial seawater containing organic matter require knowledge of the CCN activity of the inorganic component, especially as a small amount of the inorganic can heavily influence activation. Therefore, the CCN activity of both artificial sea salt and NaCl were measured and compared. Part of the discrepancy observed between the CCN activities of the two salts may be due to morphological differences, which were investigated using

  15. Analysis of Thematic Mapper data for studying the suspended matter distribution in the coastal area of the German Bight (North Sea)

    NASA Technical Reports Server (NTRS)

    Doerffer, R.; Fischer, J.; Stoessel, M.; Brockmann, C.; Grassl, H.

    1989-01-01

    Thematic Mapper data were analyzed with respect to its capability for mapping the complex structure and dynamics of suspended matter distribution in the coastal area of the German Bight (North Sea). Three independent pieces of information were found by factor analysis of all seven TM channels: suspended matter concentration, atmospheric scattering, and sea surface temperature. For the required atmospheric correction, the signal-to-noise ratios of Channels 5 and 7 have to be improved by averaging over 25 x 25 pixels, which also makes it possible to monitor the aerosol optical depth and aerosol type over cloud-free water surfaces. Near-surface suspended matter concentrations may be detected with an accuracy of factor less than 2 by using an algorithm derived from radiative transfer model calculation. The patchiness of suspended matter and its relation to underwater topography was analyzed with autocorrelation and cross-correlation.

  16. Rock encrusting assemblages: Structure and distribution along the Baltic Sea

    NASA Astrophysics Data System (ADS)

    Grabowska, Monika; Grzelak, Katarzyna; Kukliński, Piotr

    2015-09-01

    Aquatic community structure and dynamics are generally controlled by a variety of biological and physical factors. Among these factors in marine ecosystems, salinity is known to have a significant effect on species occurrence and composition. In this study, we investigated the large-scale distribution and abundance of encrusting fauna along a salinity gradient on the shallow Baltic Sea rocky coast. Rock samples collected from 14 locations distributed between the Gulf of Bothnia (salinity 0.6) and Skagerrak (salinity 28) supported a total number of 24 encrusting species. The faunas were composed mostly of marine species with opportunistic life histories; however, some brackish water specialists were also present. The number of species and abundance counts is strongly positively correlated with increases in salinity. No encrusting faunas were recorded below salinity level 4. Multivariate analysis (nMDS) revealed three major groups based on species composition that differed in terms of abundance and number of species. Each group was associated with specific salinity conditions. The first assemblage type occurred within salinity 4-7, the second within salinity between 22 and 27, and the third type was a mixture between the two observed at a salinity of approximately 17. This study indicates that to determine the assemblage structure of the Baltic Sea encrusting fauna, analyses at the family level were found to be a reliable surrogate for species composition.

  17. Accuracy Assessment of Aqua-MODIS Aerosol Optical Depth Over Coastal Regions: Importance of Quality Flag and Sea Surface Wind Speed

    NASA Technical Reports Server (NTRS)

    Anderson, J. C.; Wang, J.; Zeng, J.; Petrenko, M.; Leptoukh, G. G.; Ichoku, C.

    2012-01-01

    Coastal regions around the globe are a major source for anthropogenic aerosols in the atmosphere, but the underlying surface characteristics are not favorable for the Moderate Resolution Imaging Spectroradiometer (MODIS) algorithms designed for retrieval of aerosols over dark land or open-ocean surfaces. Using data collected from 62 coastal stations worldwide from the Aerosol Robotic Network (AERONET) from approximately 2002-2010, accuracy assessments are made for coastal aerosol optical depth (AOD) retrieved from MODIS aboard Aqua satellite. It is found that coastal AODs (at 550 nm) characterized respectively by the MODIS Dark Land (hereafter Land) surface algorithm, the Open-Ocean (hereafter Ocean) algorithm, and AERONET all exhibit a log-normal distribution. After filtering by quality flags, the MODIS AODs respectively retrieved from the Land and Ocean algorithms are highly correlated with AERONET (with R(sup 2) is approximately equal to 0.8), but only the Land algorithm AODs fall within the expected error envelope greater than 66% of the time. Furthermore, the MODIS AODs from the Land algorithm, Ocean algorithm, and combined Land and Ocean product show statistically significant discrepancies from their respective counterparts from AERONET in terms of mean, probability density function, and cumulative density function, which suggest a need for future improvement in retrieval algorithms. Without filtering with quality flag, the MODIS Land and Ocean AOD dataset can be degraded by 30-50% in terms of mean bias. Overall, the MODIS Ocean algorithm overestimates the AERONET coastal AOD by 0.021 for AOD less than 0.25 and underestimates it by 0.029 for AOD greater than 0.25. This dichotomy is shown to be related to the ocean surface wind speed and cloud contamination effects on the satellite aerosol retrieval. The Modern Era Retrospective-Analysis for Research and Applications (MERRA) reveals that wind speeds over the global coastal region 25 (with a mean and median

  18. Retrieval of Aerosol Optical Thickness and Normalized Water-Leaving Radiances From the SeaWiFS and MODIS Sensors Over the Chesapeake Bay Area (Case 2 Water)

    NASA Astrophysics Data System (ADS)

    Ahmad, Z.; Kwiatkowska, E. J.; Franz, B. A.; McClain, C. R.

    2007-12-01

    Presently, a suite of 12 aerosol models are used for atmospheric correction purposes to retrieve normalized water-leaving radiances in the visible bands of the SeaWiFS and MODIS sensors. These aerosol models are based on Shettle and Fenn's models (1979) of tropospheric and oceanic aerosols. Over most of the open oceans of the world (case 1 water), the atmospheric correction algorithm has been shown to work reasonably well. However, over case 2 waters, (for example Chesapeake Bay) the algorithm often yields negative water- leaving radiances, particularly, in the blue bands of the two sensors. In addition, over the coastal areas, the retrieved aerosol optical thickness (AOT) in the 865/869 bands are often higher than the in situ AERONET retrievals. Our analysis of the AERONET data show that Shettle and Fenn's aerosol models are not representative of the aerosols generally found over the coastal region of the Eastern United States. We show that use of wrong aerosol models often results in negative water-leaving radiances. Also, the backscattering of the solar irradiance in the near IR bands by phytoplankton and non-algal suspended particles results in overestimation of AOT. Based on the AERONET data, we have developed a set of new aerosol models for the atmospheric correction over Chesapeake Bay. Results from the new aerosol models, including comparison of satellite-derived AOT and the AERONET in the visible and near IR bands, will be presented.

  19. What drives the aerosol distribution in Guangdong - the most developed province in Southern China?

    NASA Astrophysics Data System (ADS)

    Li, Lili; Wang, Yunpeng

    2014-08-01

    This paper uses Moderate Resolution Imaging Spectroradiometer (MODIS) data to investigate the spatial and temporal variations of aerosol optical thickness (AOT) over Guangdong, the most developed province in China, during 2010-2012. Linear regression and self-organizing maps (SOM) are used to investigate the relationship between AOT and its affecting factors, including Normalized Difference Vegetation Index (NDVI), elevation, urbanized land fraction, and several socio-economic variables. Results show that the highest values of τ0.55 mainly occur over the rapidly-developing Pearl River Delta (PRD) region and the eastern coast. Seasonal averaged AOT is highest in summer (0.416), followed by spring (0.351), winter (0.292), and autumn (0.254). From unary linear regression and SOM analysis, AOT is shown to be strongly negatively correlated to NDVI (R2 = 0.782) and elevation (R2 = 0.731), and positively correlated with socio-economic factors, especially GDP, industry and vehicle density (R2 above 0.73), but not primary industry. Multiple linear regression between AOT and the contributing factors shows much higher R2 values (>0.8), indicative of the clear relationships between AOT and variables. This study illustrates that human activities have strong impacts on aerosols distribution in Guangdong Province. Economic and industrial developments, as well as vehicle density, are the main controlling factors on aerosol distribution.

  20. A new method for evaluating the impact of vertical distribution on aerosol radiative forcing in general circulation models

    NASA Astrophysics Data System (ADS)

    Vuolo, M. R.; Schulz, M.; Balkanski, Y.; Takemura, T.

    2013-07-01

    The quantification and understanding of direct aerosol forcing is essential in the study of climate. One of the main issues that makes its quantification difficult is the lack of a complete comprehension of the role of the aerosol and clouds vertical distribution. This work aims at reducing the incertitude of aerosol forcing due to the vertical superposition of several short-lived atmospheric components, in particular different aerosols species and clouds. We propose a method to quantify the contribution of different parts of the atmospheric column to the forcing, and to evaluate model differences by isolating the effect of radiative interactions only. Any microphysical or thermo-dynamical interactions between aerosols and clouds are deactivated in the model, to isolate the effects of radiative flux coupling. We investigate the contribution of aerosol above, below and in clouds, by using added diagnostics in the aerosol-climate model LMDz. We also compute the difference between the forcing of the ensemble of the aerosols and the sum of the forcings from individual species, in clear-sky. This difference is found to be moderate on global average (14%) but can reach high values regionally (up to 100%). The non-additivity of forcing already for clear-sky conditions shows, that in addition to represent well the amount of individual aerosol species, it is critical to capture the vertical distribution of all aerosols. Nonlinear effects are even more important when superposing aerosols and clouds. Four forcing computations are performed, one where the full aerosol 3-D distribution is used, and then three where aerosols are confined to regions above, inside and below clouds respectively. We find that the forcing of aerosols depends crucially on the presence of clouds and on their position relative to that of the aerosol, in particular for black carbon (BC). We observe a strong enhancement of the forcing of BC above clouds, attenuation for BC below clouds, and a moderate

  1. Aerosols, clouds, and precipitation in the North Atlantic trades observed during the Barbados aerosol cloud experiment - Part 1: Distributions and variability

    NASA Astrophysics Data System (ADS)

    Jung, Eunsil; Albrecht, Bruce A.; Feingold, Graham; Jonsson, Haflidi H.; Chuang, Patrick; Donaher, Shaunna L.

    2016-07-01

    Shallow marine cumulus clouds are by far the most frequently observed cloud type over the Earth's oceans; but they are poorly understood and have not been investigated as extensively as stratocumulus clouds. This study describes and discusses the properties and variations of aerosol, cloud, and precipitation associated with shallow marine cumulus clouds observed in the North Atlantic trades during a field campaign (Barbados Aerosol Cloud Experiment- BACEX, March-April 2010), which took place off Barbados where African dust periodically affects the region. The principal observing platform was the Center for Interdisciplinary Remotely Piloted Aircraft Studies (CIRPAS) Twin Otter (TO) research aircraft, which was equipped with standard meteorological instruments, a zenith pointing cloud radar and probes that measured aerosol, cloud, and precipitation characteristics.The temporal variation and vertical distribution of aerosols observed from the 15 flights, which included the most intense African dust event during all of 2010 in Barbados, showed a wide range of aerosol conditions. During dusty periods, aerosol concentrations increased substantially in the size range between 0.5 and 10 µm (diameter), particles that are large enough to be effective giant cloud condensation nuclei (CCN). The 10-day back trajectories showed three distinct air masses with distinct vertical structures associated with air masses originating in the Atlantic (typical maritime air mass with relatively low aerosol concentrations in the marine boundary layer), Africa (Saharan air layer), and mid-latitudes (continental pollution plumes). Despite the large differences in the total mass loading and the origin of the aerosols, the overall shapes of the aerosol particle size distributions were consistent, with the exception of the transition period.The TO was able to sample many clouds at various phases of growth. Maximum cloud depth observed was less than ˜ 3 km, while most clouds were less than 1 km

  2. Spatial distribution of aerosol black carbon over India during pre-monsoon season

    NASA Astrophysics Data System (ADS)

    Beegum, S. Naseema; Moorthy, K. Krishna; Babu, S. Suresh; Satheesh, S. K.; Vinoj, V.; Badarinath, K. V. S.; Safai, P. D.; Devara, P. C. S.; Singh, Sacchidanand; Vinod; Dumka, U. C.; Pant, P.

    Aerosol black carbon (BC) mass concentrations ([BC]), measured continuously during a mutli-platform field experiment, Integrated Campaign for Aerosols gases and Radiation Budget (ICARB, March-May 2006), from a network of eight observatories spread over geographically distinct environments of India, (which included five mainland stations, one highland station, and two island stations (one each in Arabian Sea and Bay of Bengal)) are examined for their spatio-temporal characteristics. During the period of study, [BC] showed large variations across the country, with values ranging from 27 μg m -3 over industrial/urban locations to as low as 0.065 μg m -3 over the Arabian Sea. For all mainland stations, [BC] remained high compared to highland as well as island stations. Among the island stations, Port Blair (PBR) had higher concentration of BC, compared to Minicoy (MCY), implying more absorbing nature of Bay of Bengal aerosols than Arabian Sea. The highland station Nainital (NTL), in the central Himalayas, showed low values of [BC], comparable or even lower than that of the island station PBR, indicating the prevalence of cleaner environment over there. An examination of the changes in the mean temporal features, as the season advances from winter (December-February) to pre-monsoon (March-May), revealed that: (a) Diurnal variations were pronounced over all the mainland stations, with an afternoon low and a nighttime high; (b) At the islands, the diurnal variations, though resembled those over the mainlands, were less pronounced; and (c) In contrast to this, highland station showed an opposite pattern with an afternoon high and a late night or early morning low. The diurnal variations at all stations are mainly caused by the dynamics of local Atmospheric Boundary Layer (ABL). At the entire mainland as well as island stations (except HYD and DEL), [BC] showed a decreasing trend from January to May. This is attributed to the increased convective mixing and to the

  3. Measuring Bipolar Charge and Mass Distributions of Powder Aerosols by a Novel Tool (BOLAR).

    PubMed

    Wong, Jennifer; Lin, Yu-Wei; Kwok, Philip Chi Lip; Niemelä, Ville; Crapper, John; Chan, Hak-Kim

    2015-09-01

    The Bipolar Charge Analyzer (BOLAR) was evaluated for measuring bipolar electrostatic charge and mass distributions of powder aerosols generated from a dry powder inhaler. Mannitol powder (5, 10, and 20 mg) was dispersed using an Osmohaler inhaler into the BOLAR at air flow rates of 30 or 60 L/min. As the aerosol sample was drawn through the BOLAR, the air flow was divided into six equal fractions. Five of them entered individual detection tubes with a defined cutoff diameter in the range of 0.95 to 16.36 μm (depending on the flow rate) and the remaining (i.e., the sixth) fraction passed through a reference chamber. The aerosols that entered the detection tubes were separated according to the particle charge polarity (positive, negative, or neutral) and charge was measured by separate electrometers. The deposited powder of a single actuation from the inhaler was chemically assayed using high performance liquid chromatography. Additionally, the aerosol measurements were conducted on a modified Classic Electrical Low Pressure Impactor (ELPI) for comparison of the net specific charge per size fraction. Spray-dried mannitol carried significantly different positively and negatively charged particles in each of the five defined particle size fractions. The charge-to-mass ratio (q/m) of positively charged particles ranged from +1.11 to +32.57 pC/μg and negatively charged particles ranged from -1.39 to -9.25 pC/μg, resulting in a net q/m of -3.08 to +13.34 pC/μg. The net q/m values obtained on the modified ELPI ranged from -5.18 to +4.81 pC/μg, which were comparable to the BOLAR measurements. This is the first full report to utilize the BOLAR to measure bipolar charge and mass distributions of a powder aerosol. Positively and negatively charged particles were observed within each size fraction, and their corresponding q/m profiles were successfully characterized. Despite some potential drawbacks, the BOLAR has provided a new platform for investigating bipolar charge

  4. 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

  5. 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.

  6. The weather dependence of particle size distribution of indoor radioactive aerosol associated with radon decay products.

    PubMed

    Mostafa, A M A; Tamaki, K; Moriizumi, J; Yamazawa, H; Iida, T

    2011-07-01

    This study was performed to measure the activity size distribution of aerosol particles associated with short-lived radon decay products in indoor air at Nagoya University, Nagoya, Japan. The measurements were performed using a low pressure Andersen cascade impactor under variable meteorological conditions. The results showed that the greatest activity fraction was associated with aerosol particles in the accumulation size range (100-1000 nm) with a small fraction of nucleation mode (10-100 nm). Regarding the influence of the weather conditions, the decrease in the number of accumulation particles was observed clearly after rainfall without significant change in nucleation particles, which may be due to a washout process for the large particles.

  7. Global and regional trends of aerosol optical depth over land and ocean using SeaWiFS measurements from 1997 to 2010

    NASA Astrophysics Data System (ADS)

    Hsu, N. C.; Gautam, R.; Sayer, A. M.; Bettenhausen, C.; Li, C.; Jeong, M. J.; Tsay, S.-C.; Holben, B. N.

    2012-09-01

    Both sensor calibration and satellite retrieval algorithm play an important role in the ability to determine accurately long-term trends from satellite data. Owing to the unprecedented accuracy and long-term stability of its radiometric calibration, SeaWiFS measurements exhibit minimal uncertainty with respect to sensor calibration. In this study, we take advantage of this well-calibrated set of measurements by applying a newly-developed aerosol optical depth (AOD) retrieval algorithm over land and ocean to investigate the distribution of AOD, and to identify emerging patterns and trends in global and regional aerosol loading during its 13-yr mission. Our correlation analysis between climatic indices (such as ENSO) and AOD suggests strong relationships for Saharan dust export as well as biomass-burning activity in the tropics, associated with large-scale feedbacks. The results also indicate that the averaged AOD trend over global ocean is weakly positive from 1998 to 2010 and comparable to that observed by MODIS but opposite in sign to that observed by AVHRR during overlapping years. On regional scales, distinct tendencies are found for different regions associated with natural and anthropogenic aerosol emission and transport. For example, large upward trends are found over the Arabian Peninsula that indicate a strengthening of the seasonal cycle of dust emission and transport processes over the whole region as well as over downwind oceanic regions. In contrast, a negative-neutral tendency is observed over the desert/arid Saharan region as well as in the associated dust outflow over the north Atlantic. Additionally, we found decreasing trends over the eastern US and Europe, and increasing trends over countries such as China and India that are experiencing rapid economic development. In general, these results are consistent with those derived from ground-based AERONET measurements.

  8. Dependence of aerosol scattering coefficients on relative humidity observed at two coastal sites on the East China Sea: Comparison to remote observations and influence of chemical composition

    NASA Astrophysics Data System (ADS)

    Kanaya, Y.; Taketani, F.; Irie, H.; Komazaki, Y.; Takashima, H.; Xiaole, P.; Takami, A.; Wang, Z.

    2011-12-01

    We employed an integrating nephelometer equipped with a humidifier (where the relative humidity (RH) was scanned between 40 and 90%) to measure the aerosol scattering coefficients and their dependence on RH at Fukue Island (32.75N, 128.68E), west of Japan, in May 2009 and at Rudong, Jiangsu, China (32.26N, 121.37E) in May/June 2010, aiming at better characterization of optical properties of the regional-scale aerosol pollution over East Asia. The two coastal sites are located east and west of the East China Sea and are separated by about 700 km. The observed scattering coefficients are normalized by the concurrently measured PM2.5 mass concentrations and thereby behaviors of the mass scattering coefficients are discussed. At Fukue, the mass scattering coefficients under the ambient RH conditions were >1.5 times higher than those observed under the dry condition (RH = 40%), suggesting that the RH effect was crucial in determining optical properties under ambient conditions. The coefficients under the ambient RH conditions, rather than the dry values, agreed better with the extinction coefficients determined by MAX-DOAS (Multi-Axis Differential Optical Absorption Spectroscopy) technique based on remote measurements of O4 optical depths. The single-scattering albedo (SSA), estimated in combination to the absorption coefficients determined by a MAAP (Multi-Angle Absorption Photometer) instrument, had similar average values (~0.95) at the two sites. The SSA values at the two sites were commonly lowered (to below 0.90) when the air traveled from the North China Plain region. At Fukue, the RH dependence was found to be weakened when the organics/sulfate ratio increased (as observed by an Aerodyne Aerosol Mass Spectrometer), while such influence of chemical composition was less clear at Rudong, possibly masked by large temporal variations in the particle size distributions.

  9. Size distribution and optical properties of mineral dust aerosols transported in the western Mediterranean

    NASA Astrophysics Data System (ADS)

    Denjean, C.; Cassola, F.; Mazzino, A.; Triquet, S.; Chevaillier, S.; Grand, N.; Bourrianne, T.; Momboisse, G.; Sellegri, K.; Schwarzenbock, A.; Freney, E.; Mallet, M.; Formenti, P.

    2016-02-01

    This study presents in situ aircraft measurements of Saharan mineral dust transported over the western Mediterranean basin in June-July 2013 during the ChArMEx/ADRIMED (the Chemistry-Aerosol Mediterranean Experiment/Aerosol Direct Radiative Impact on the regional climate in the MEDiterranean region) airborne campaign. Dust events differing in terms of source region (Algeria, Tunisia and Morocco), time of transport (1-5 days) and height of transport were sampled. Mineral dust were transported above the marine boundary layer, which conversely was dominated by pollution and marine aerosols. The dust vertical structure was extremely variable and characterized by either a single layer or a more complex and stratified structure with layers originating from different source regions. Mixing of mineral dust with pollution particles was observed depending on the height of transport of the dust layers. Dust layers carried a higher concentration of pollution particles below 3 km above sea level (a.s.l.) than above 3 km a.s.l., resulting in a scattering Ångström exponent up to 2.2 below 3 km a.s.l. However, the optical properties of the dust plumes remained practically unchanged with respect to values previously measured over source regions, regardless of the altitude. Moderate absorption of light by the dust plumes was observed with values of aerosol single scattering albedo at 530 nm ranging from 0.90 to 1.00. Concurrent calculations from the aerosol chemical composition revealed a negligible contribution of pollution particles to the absorption properties of the dust plumes that was due to a low contribution of refractory black carbon in regards to the fraction of dust and sulfate particles. This suggests that, even in the presence of moderate pollution, likely a persistent feature in the Mediterranean, the optical properties of the dust plumes could be assumed similar to those of native dust in radiative transfer simulations, modelling studies and satellite retrievals

  10. Multi-peak accumulation and coarse modes observed from AERONET retrieved aerosol volume size distribution in Beijing

    NASA Astrophysics Data System (ADS)

    Zhang, Ying; Li, Zhengqiang; Zhang, Yuhuan; Chen, Yu; Cuesta, Juan; Ma, Yan

    2016-08-01

    We present characteristic peaks of atmospheric columnar aerosol volume size distribution retrieved from the AErosol RObotic NETwork (AERONET) ground-based Sun-sky radiometer observation, and their correlations with aerosol optical properties and meteorological conditions in Beijing over 2013. The results show that the aerosol volume particle size distribution (VPSD) can be decomposed into up to four characteristic peaks, located in accumulation and coarse modes, respectively. The mean center radii of extra peaks in accumulation and coarse modes locate around 0.28 (±0.09) to 0.38 (±0.11) and 1.25 (±0.56) to 1.47 (±0.30) μm, respectively. The multi-peak size distributions are found in different aerosol loading conditions, with the mean aerosol optical depth (440 nm) of 0.58, 0.49, 1.18 and 1.04 for 2-, 3-I/II and 4-peak VPSD types, while the correspondingly mean relative humidity values are 58, 54, 72 and 67 %, respectively. The results also show the significant increase (from 0.25 to 0.40 μm) of the mean extra peak median radius in the accumulation mode for the 3-peak-II cases, which agrees with aerosol hygroscopic growth related to relative humidity and/or cloud or fog processing.

  11. Individual Aerosol Particles from Biomass Burning in Southern Africa. 1; Compositions and Size Distributions of Carbonaceous Particles

    NASA Technical Reports Server (NTRS)

    Posfai, Mihaly; Simonics, Renata; Li, Jia; Hobbs, Peter V.; Buseck, Peter R.

    2003-01-01

    Individual aerosol particles in smoke plumes from biomass fires and in regional hazes in southern Africa were studied using analytical transmission electron microscopy (TEM), which allowed detailed characterization of carbonaceous particle types in smoke and determination of changes in particle properties and concentrations during smoke aging. Based on composition, morphology, and microstructure, three distinct types of carbonaceous particles were present in the smoke: organic particles with inorganic (K-salt) inclusions, tar ball particles, and soot. The relative number concentrations of organic particles were largest in young smoke, whereas tar balls were dominant in a slightly aged (1 hour) smoke from a smoldering fire. Flaming fires emitted relatively more soot particles than smoldering fires, but soot was a minor constituent of all studied plumes. Further aging caused the accumulation of sulfate on organic and soot particles, as indicated by the large number of internally mixed organic/sulfate and soot/sulfate particles in the regional haze. Externally mixed ammonium sulfate particles dominated in the boundary layer hazes, whereas organic/sulfate particles were the most abundant type in the upper hazes. Apparently, elevated haze layers were more strongly affected by biomass smoke than those within the boundary layer. Based on size distributions and the observed patterns of internal mixing, we hypothesize that organic and soot particles are the cloud-nucleating constituents of biomass smoke aerosols. Sea-salt particles dominated in the samples taken in stratus clouds over the Atlantic Ocean, off the coast of Namibia, whereas a distinct haze layer above the clouds consisted of aged biomass smoke particles.

  12. Diversity and distribution of deep-sea shrimps in the Ross Sea region of Antarctica.

    PubMed

    Basher, Zeenatul; Bowden, David A; Costello, Mark J

    2014-01-01

    Although decapod crustaceans are widespread in the oceans, only Natantia (shrimps) are common in the Antarctic. Because remoteness, depth and ice cover restrict sampling in the South Ocean, species distribution modelling is a useful tool for evaluating distributions. We used physical specimen and towed camera data to describe the diversity and distribution of shrimps in the Ross Sea region of Antarctica. Eight shrimp species were recorded: Chorismus antarcticus; Notocrangon antarcticus; Nematocarcinus lanceopes; Dendrobranchiata; Pasiphaea scotiae; Pasiphaea cf. ledoyeri; Petalidium sp., and a new species of Lebbeus. For the two most common species, N. antarcticus and N. lanceopes, we used maximum entropy modelling, based on records of 60 specimens and over 1130 observations across 23 sites in depths from 269 m to 3433 m, to predict distributions in relation to environmental variables. Two independent sets of environmental data layers at 0.05° and 0.5° resolution respectively, showed how spatial resolution affected the model. Chorismus antarcticus and N. antarcticus were found only on the continental shelf and upper slopes, while N. lanceopes, Lebbeus n. sp., Dendrobranchiata, Petalidium sp., Pasiphaea cf. ledoyeri, and Pasiphaea scotiae were found on the slopes, seamounts and abyssal plain. The environmental variables that contributed most to models for N. antarcticus were depth, chlorophyll-a concentration, temperature, and salinity, and for N. lanceopes were depth, ice concentration, seabed slope/rugosity, and temperature. The relative ranking, but not the composition of these variables changed in models using different spatial resolutions, and the predicted extent of suitable habitat was smaller in models using the finer-scale environmental layers. Our modelling indicated that shrimps were widespread throughout the Ross Sea region and were thus likely to play important functional role in the ecosystem, and that the spatial resolution of data needs to be

  13. Diversity and distribution of deep-sea shrimps in the Ross Sea region of Antarctica.

    PubMed

    Basher, Zeenatul; Bowden, David A; Costello, Mark J

    2014-01-01

    Although decapod crustaceans are widespread in the oceans, only Natantia (shrimps) are common in the Antarctic. Because remoteness, depth and ice cover restrict sampling in the South Ocean, species distribution modelling is a useful tool for evaluating distributions. We used physical specimen and towed camera data to describe the diversity and distribution of shrimps in the Ross Sea region of Antarctica. Eight shrimp species were recorded: Chorismus antarcticus; Notocrangon antarcticus; Nematocarcinus lanceopes; Dendrobranchiata; Pasiphaea scotiae; Pasiphaea cf. ledoyeri; Petalidium sp., and a new species of Lebbeus. For the two most common species, N. antarcticus and N. lanceopes, we used maximum entropy modelling, based on records of 60 specimens and over 1130 observations across 23 sites in depths from 269 m to 3433 m, to predict distributions in relation to environmental variables. Two independent sets of environmental data layers at 0.05° and 0.5° resolution respectively, showed how spatial resolution affected the model. Chorismus antarcticus and N. antarcticus were found only on the continental shelf and upper slopes, while N. lanceopes, Lebbeus n. sp., Dendrobranchiata, Petalidium sp., Pasiphaea cf. ledoyeri, and Pasiphaea scotiae were found on the slopes, seamounts and abyssal plain. The environmental variables that contributed most to models for N. antarcticus were depth, chlorophyll-a concentration, temperature, and salinity, and for N. lanceopes were depth, ice concentration, seabed slope/rugosity, and temperature. The relative ranking, but not the composition of these variables changed in models using different spatial resolutions, and the predicted extent of suitable habitat was smaller in models using the finer-scale environmental layers. Our modelling indicated that shrimps were widespread throughout the Ross Sea region and were thus likely to play important functional role in the ecosystem, and that the spatial resolution of data needs to be

  14. Diversity and Distribution of Deep-Sea Shrimps in the Ross Sea Region of Antarctica

    PubMed Central

    Basher, Zeenatul; Bowden, David A.; Costello, Mark J.

    2014-01-01

    Although decapod crustaceans are widespread in the oceans, only Natantia (shrimps) are common in the Antarctic. Because remoteness, depth and ice cover restrict sampling in the South Ocean, species distribution modelling is a useful tool for evaluating distributions. We used physical specimen and towed camera data to describe the diversity and distribution of shrimps in the Ross Sea region of Antarctica. Eight shrimp species were recorded: Chorismus antarcticus; Notocrangon antarcticus; Nematocarcinus lanceopes; Dendrobranchiata; Pasiphaea scotiae; Pasiphaea cf. ledoyeri; Petalidium sp., and a new species of Lebbeus. For the two most common species, N. antarcticus and N. lanceopes, we used maximum entropy modelling, based on records of 60 specimens and over 1130 observations across 23 sites in depths from 269 m to 3433 m, to predict distributions in relation to environmental variables. Two independent sets of environmental data layers at 0.05° and 0.5° resolution respectively, showed how spatial resolution affected the model. Chorismus antarcticus and N. antarcticus were found only on the continental shelf and upper slopes, while N. lanceopes, Lebbeus n. sp., Dendrobranchiata, Petalidium sp., Pasiphaea cf. ledoyeri, and Pasiphaea scotiae were found on the slopes, seamounts and abyssal plain. The environmental variables that contributed most to models for N. antarcticus were depth, chlorophyll-a concentration, temperature, and salinity, and for N. lanceopes were depth, ice concentration, seabed slope/rugosity, and temperature. The relative ranking, but not the composition of these variables changed in models using different spatial resolutions, and the predicted extent of suitable habitat was smaller in models using the finer-scale environmental layers. Our modelling indicated that shrimps were widespread throughout the Ross Sea region and were thus likely to play important functional role in the ecosystem, and that the spatial resolution of data needs to be

  15. Distributions and sea-to-air fluxes of nitrous oxide in the South China Sea and the West Philippines Sea

    NASA Astrophysics Data System (ADS)

    Tseng, Hsiao-Chun; Chen, Chen-Tung Arthur; Borges, Alberto V.; DelValls, T. Angel; Lai, Chao-Ming; Chen, Ting-Yu

    2016-09-01

    Approximately 600 water samples from the South China Sea (SCS) and 250 water samples from the West Philippines Sea (WPS) were collected during seven cruises from August 2003 to July 2007 to determine nitrous oxide (N2O) distributions between the surface and a maximum depth of 4250 m. In the SCS, the average surface N2O concentration exceeded the atmospheric equilibrium concentration (on average 132±23%); however in the WPS, the surface N2O concentration was lower than the atmospheric equilibrium concentration (on average 90±22%). The N2O concentration reached a maximum (~23 nmol L-1) in the WPS at 800-1000 m, and (~28 nmol L-1) at a shallower depth of around 600-800 m in the SCS, owing to vertical mixing and intensive upwelling in the SCS. In the SCS, the surface N2O concentration was 7.59±1.32 nmol L-1 and the calculated sea-to-air flux was 5.5±3.9 μmol m-2 d-1. The surface N2O concentration in the WPS, 5.19±1.26 nmol L-1, was lower than that in the SCS. The WPS is a sink for N2O and the calculated sea-to-air flux was -1.7±3.9 μmol m-2 d-1. The SCS emitted 19.3×106 mol d-1 N2O to the atmosphere and exported 8.5×106 mol d-1 N2O to the WPS during the wet season.

  16. Vertical distribution of marine cyanobacteria Synechococcus spp. in the Black, Marmara, Aegean, and eastern Mediterranean seas

    NASA Astrophysics Data System (ADS)

    Uysal, Zahit

    2006-08-01

    The vertical distributions of the unicellular cyanobacteria Synechococcus were studied in several highly contrasting seas: the Black Sea, Sea of Marmara, Aegean Sea, and Mediterranean Sea. Cell abundances varied significantly on both vertical and horizontal scales in all physically and spatially discrete water masses. Epifluorescence microscope cell counts from all seas clearly showed that majority of the population remains suspended in the surface-mixed layer and decreases gradually towards the base of the euphotic zone. Surface spatial distributions in the Black Sea were heterogeneous. Salinity, rather than temperature, seemed to have the greatest impact on the surface distribution of cells in this highly eutrophic sea. Changes in abundance in the mixed layer were small compared to the abrupt changes below the halocline, especially in the Black Sea and the Sea of Marmara. In contrast to the Black Sea, the major population remains suspended above the depth of fluorescence maximum in the Aegean and eastern Mediterranean seas. Significant correlations ( r>P0.01) were observed between cell counts and physical and chemical parameters with depth in the Black Sea. In all seas, cells at subsurface chlorophyll- a maximum layer (SCML) reflected brighter and longer fluorescence than those present at the surface and below. Cell size derived from flow cytometry indicated the presence of larger cells at the surface mixed layer compared to those at depth.

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

    NASA Astrophysics Data System (ADS)

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

    2015-12-01

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

  18. On the correlation of atmospheric aerosol components of mass size distributions in the larger region of a central European city

    NASA Astrophysics Data System (ADS)

    Berner, A.; Galambos, Z.; Ctyroky, P.; Frühauf, P.; Hitzenberger, R.; Gomišček, B.; Hauck, H.; Preining, O.; Puxbaum, H.

    Mass size distributions of atmospheric aerosols have been sampled in the region of Vienna, a typical city in central Europe, at an urban and a rural site. The aerosol was collected simultaneously by cascade impactors. Two experiments which had a duration of 4 weeks each, were performed in August 1999 and in January/February 2000. Daily sampling periods were from 8:00 to 20:00, and from 20:00 to 8:00. An evaluation of the mass size distributions is represented in this paper. Emphasis is on the relationships of different aerosol components in a local and a regional context. The main results are as follows. The main components of the atmospheric aerosol are a fine aerosol, the accumulation aerosol, and a coarse aerosol. Specific coarse modes with modal diameters of 4.7 μm average and geometric standard deviations of about 3 occur at the urban and at the rural site, some times surprisingly strong. The fine and the coarse modes are very likely related to motor-car traffic. Usually the PM 2.5 and PM 10 aerosols are regionally strongly correlated. Occasionally, this correlation is effectively disturbed by local and/or regional emissions. Time series of correlation coefficients reveal an episodic character of the atmospheric aerosol. Periods of strong inter-site correlations of PM 2.5 and PM 10 indicate the dominance and the co-variation of the accumulation aerosols or the dominance and the co-variation of the coarse modes.

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

    NASA Astrophysics Data System (ADS)

    Hitzenberger, R.; Tohno, S.

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

  20. A statistical analysis of North East Atlantic (submicron) aerosol size distributions

    NASA Astrophysics Data System (ADS)

    Dall'Osto, M.; Monahan, C.; Greaney, R.; Beddows, D. C. S.; Harrison, R. M.; Ceburnis, D.; O'Dowd, C. D.

    2011-08-01

    The Global Atmospheric Watch research station at Mace Head (Ireland) offers the possibility to sample some of the cleanest air masses being imported into Europe as well as some of the most polluted being exported out of Europe. We present a statistical Cluster~analysis of the physical characteristics of aerosol size distributions in air ranging from the cleanest to the most polluted for the year 2008. Data coverage achieved was 75 % throughout the year. By applying the Hartigan-Wong k-Means method, 12 Clusters were identified as systematically occurring and these 12 Clusters could be further combined into 4 categories with similar characteristics, namely: coastal nucleation category (occurring 21.3 % of the time), open ocean nucleation category (occurring 32.6 % of the time), background clean marine category (occurring 26.1 % of the time) and anthropogenic category (occurring 20 % of the time) aerosol size distributions. The coastal nucleation category is characterised by a clear and dominant nucleation mode at sizes less that 10 nm while the open ocean nucleation category is characterised by a dominant Aitken mode between 15 nm and 50 nm. The background clean marine characteristic is a clear bimodality in the size distribution, although it should be noted that either the Aitken mode or the Accumulation mode may dominate the number concentration. By contrast, the continentally-influenced size distributions are generally more mono-modal, albeit with traces of bi-modality. The open ocean category occurs more often during May, June and July, corresponding with the N. E. Atlantic high biological period. Combined with the relatively high percentage frequency of occurrence (32.6 %), this suggests that the marine biota is an important source of new aerosol particles in N. E. Atlantic Air.

  1. Size distribution dynamics reveal particle-phase chemistry in organic aerosol formation

    NASA Astrophysics Data System (ADS)

    Shiraiwa, M.; Yee, L. D.; Schilling, K.; Loza, C. L.; Craven, J. S.; Zuend, A.; Ziemann, P. J.; Seinfeld, J.

    2013-12-01

    Organic aerosols are ubiquitous in the atmosphere and play a central role in climate, air quality and public health. The aerosol size distribution is key in determining its optical properties and cloud condensation nucleus activity. The dominant portion of organic aerosol is formed through gas-phase oxidation of volatile organic compounds, so-called secondary organic aerosol (SOA). Typical experimental measurements of SOA formation include total SOA mass and atomic oxygen-to-carbon ratio. These measurements, alone, are generally insufficient to reveal the extent to which condensed-phase reactions occur in conjunction with the multi-generation gas-phase photooxidation. Combining laboratory chamber experiments and kinetic gas-particle modeling for the dodecane SOA system, here we show that the presence of particle-phase chemistry is reflected in the evolution of the SOA size distribution as well as its mass concentration. Particle-phase reactions are predicted to occur mainly at the particle surface and the reaction products contribute more than half of the SOA mass. Chamber photooxidation with a mid-experiment aldehyde injection confirms that heterogeneous reaction of aldehydes with organic hydroperoxides forming peroxyhemiacetals can lead to a large increase in SOA mass. The results of the current work have a number of implications for SOA models. While the dynamics of an aerosol size distribution reflects the mechanism of growth, we demonstrate here that it provides a key constraint in interpreting laboratory and ambient SOA formation. This work, although carried out specifically for the long chain alkane, dodecane, is expected to be widely applicable to other major classes of SOA precursors. SOA consists of a myriad of organic compounds containing various functional groups, which can generally undergo heterogeneous/multiphase reactions forming low-volatility products such as oligomers and other high molecular mass compounds. If particle-phase chemistry is indeed

  2. Distribution of phosphorus in the eastern Adriatic Sea sediments (Croatia)

    NASA Astrophysics Data System (ADS)

    Matijević, Slavica; Bogner, Danijela; Kušpilić, Grozdan; Veža, Jere

    2014-05-01

    Phosphorus (P) is very important nutrient for the eastern Adriatic Sea owing to its limiting role in the primary production. Orthophosphate concentrations are low (median HPO42- value: 0.039 µmol dm-3) as a consequence of relatively small number of freshwater inflows and cyclonic circulation of oligotrophic eastern Mediterranean water masses. Due to anthropogenic influence in coastal areas such as bays, estuaries and channel waters, P concentrations increment occurred leading to the formation of trophic gradient from the open sea towards the coast. As marine sediment presents the ultimate sink for particulate organic P from the water column, as well as for inorganic P forms, knowledge about distribution of different sediment P species is of great importance for understanding the burial, diagenesis and environmental geochemical significance of P. This paper presents results of P distribution at the eastern Adriatic sites of different trophic status (open sea, channel, estuary, semi-enclosed bay under the anthropogenic influence and fish farms) during 2002-2012. In the water column dissolved and particulate inorganic and organic P were analyzed. In all sediments total phosphorus (organic and inorganic P) was determined, while at certain sites beside organic P, inorganic P forms were examined using modified SEDEX methods (P in biogenic - P-FD; authigenic - P-AUT and in detrital apatite - P-DET; phosphorus bound to iron oxides and hydroxides - P-Fe). Various geochemical variables in the water column and sediment (HPO42- concentration, sediment redox potential, granulometric composition, carbonate content, iron, organic carbon and total nitrogen content) were also investigated. Results proved total P concentrations range between 3 and 161 µmol g-1, with highest values at sites under the strong anthropogenic impact including fish farms, estuaries and bay areas. Major inorganic P species in the eastern Adriatic was P-Fe form. Fish debris P species P-FD, prevailed in

  3. Particle size distribution of radioactive aerosols after the Fukushima and the Chernobyl accidents.

    PubMed

    Malá, Helena; Rulík, Petr; Bečková, Vera; Mihalík, Ján; Slezáková, Miriam

    2013-12-01

    Following the Fukushima accident, a series of aerosol samples were taken between 24th March and 13th April 2011 by cascade impactors in the Czech Republic to obtain the size distribution of (131)I, (134)Cs, (137)Cs, and (7)Be aerosols. All distributions could be considered monomodal. The arithmetic means of the activity median aerodynamic diameters (AMADs) for artificial radionuclides and for (7)Be were 0.43 and 0.41 μm with GDSs 3.6 and 3.0, respectively. The time course of the AMADs of (134)Cs, (137)Cs and (7)Be in the sampled period showed a slight decrease at a significance level of 0.05, whereas the AMAD pertaining to (131)I increased at a significance level of 0.1. Results obtained after the Fukushima accident were compared with results obtained after the Chernobyl accident. The radionuclides released during the Chernobyl accident for which we determined the AMAD fell into two categories: refractory radionuclides ((140)Ba, (140)La (141)Ce, (144)Ce, (95)Zr and (95)Nb) and volatile radionuclides ((134)Cs, (137)Cs, (103)Ru, (106)Ru, (131)I, and (132)Te). The AMAD of the refractory radionuclides was approximately 3 times higher than the AMAD of the volatile radionuclides; nevertheless, the size distributions for volatile radionuclides having a mean AMAD value of 0.51 μm were very close to the distributions after the Fukushima accident.

  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.

    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

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