Modelling atmospheric deposition flux of Cadmium and Lead in urban areas

International Nuclear Information System (INIS)

Cherin, Nicolas

2017-01-01

According to WHO, air pollution is responsible for more than 3.7 million premature deaths each year (OMS, 2014). Moreover, among these deaths, more than 70 within urban areas. Consequently, the health and environmental impacts of pollutants within these urban areas are of great concern in air quality studies. The deposition fluxes of air pollutants, which can be significant near sources of pollution, have rarely been modeled within urban areas. Historically, atmospheric deposition studies have focused mostly on remote areas to assess the potential impacts on ecosystems of acid deposition and nitrogen loading. Therefore, current atmospheric deposition models may not be suitable to simulate deposition fluxes in urban areas, which include complex surface geometries and diverse land use types. Atmospheric dry deposition is typically modeled using an average roughness length, which depends on land use. This classical roughness-length approach cannot account for the spatial variability of dry deposition in complex settings such as urban areas. Urban canopy models have been developed to parameterize momentum and heat transfer. We extend this approach here to mass transfer, and a new dry deposition model based on the urban canyon concept is presented. It uses a local mixing-length parameterization of turbulence within the canopy, and a description of the urban canopy via key parameters to provide spatially distributed dry deposition fluxes. This approach provides spatially distributed dry deposition fluxes depending on surfaces (streets, walls, roofs) and flow regimes (recirculation and ventilation) within the urban area. (author) [fr

Mechanisms and rates of atmospheric deposition of selected trace elements and sulfate to a deciduous forest watershed. [Roles of dry and wet deposition concentrations measured in Walker Branch Watershed

Energy Technology Data Exchange (ETDEWEB)

Lindberg, S.E.; Harriss, R.C.; Turner, R.R.; Shriner, D.S.; Huff, D.D.

1979-06-01

The critical links between anthropogenic emissions to the atmosphere and their effects on ecosystems are the mechanisms and rates of atmospheric deposition. The atmospheric input of several trace elements and sulfate to a deciduous forest canopy is quantified and the major mechanisms of deposition are determined. The study area was Walker Branch Watershed (WBW) in eastern Tennessee. The presence of a significant quantity of fly ash and dispersed soil particles on upward-facing leaf and flat surfaces suggested sedimentation to be a major mechanism of dry deposition to upper canopy elements. The agreement for deposition rates measured to inert, flat surfaces and to leaves was good for Cd, SO/sub 4//sup =/, Zn, and Mn but poor for Pb. The precipitation concentrations of H/sup +/, Pb, Mn, and SO/sub 4//sup =/ reached maximum values during the summer months. About 90% of the wet deposition of Pb and SO/sub 4//sup =/ was attributed to scavenging by in-cloud processes while for Cd and Mn, removal by in-cloud scavenging accounted for 60 to 70% of the deposition. The interception of incoming rain by the forest canopy resulted in a net increase in the concentrations of Cd, Mn, Pb, Zn, and SO/sub 4//sup =/ but a net decrease in the concentration of H/sup +/. The source of these elements in the forest canopy was primarily dry deposited aerosols for Pb, primarily internal plant leaching for Mn, Cd, and Zn, and an approximately equal combination of the two for SO/sub 4//sup =/. Significant fractions of the total annual elemental flux to the forest floor in a representative chestnut oak stand were attributable to external sources for Pb (99%), Zn (44%), Cd (42%), SO/sub 4//sup =/ (39%), and Mn (14%), the remainder being related to internal element cycling mechanisms. On an annual scale the dry deposition process constituted a significant fraction of the total atmospheric input. (ERB)

Methodology and significance of studies of atmospheric deposition in highway runoff

Science.gov (United States)

Colman, John A.; Rice, Karen C.; Willoughby, Timothy C.

2001-01-01

Atmospheric deposition and the processes that are involved in causing and altering atmospheric deposition in relation to highway surfaces and runoff were evaluated nationwide. Wet deposition is more easily monitored than dry deposition, and data on wet deposition are available for major elements and water properties (constituents affecting acid deposition) from the inter-agency National Atmospheric Deposition Program/ National Trends Network (NADP/NTN). Many trace constituents (metals and organic compounds) of interest in highway runoff loads, however, are not included in the NADP/NTN. Dry deposition, which constitutes a large part of total atmospheric deposition for many constituents in highway runoff loads, is difficult to monitor accurately. Dry-deposition rates are not widely available.Many of the highway-runoff investigations that have addressed atmospheric-deposition sources have had flawed investigative designs or problems with methodology. Some results may be incorrect because of reliance on time-aggregated data collected during a period of changing atmospheric emissions. None of the investigations used methods that could accurately quantify the part of highway runoff load that can be attributed to ambient atmospheric deposition. Lack of information about accurate ambient deposition rates and runoff loads was part of the problem. Samples collected to compute the rates and loads were collected without clean-sampling methods or sampler protocols, and without quality-assurance procedures that could validate the data. Massbudget calculations comparing deposition and runoff did not consider loss of deposited material during on-highway processing. Loss of deposited particles from highway travel lanes could be large, as has been determined in labeled particle studies, because of resuspension caused by turbulence from passing traffic. Although a cause of resuspension of large particles, traffic turbulence may increase the rate of deposition for small particles and

Improved Formulations for Air-Surface Exchanges Related to National Security Needs: Dry Deposition Models

Energy Technology Data Exchange (ETDEWEB)

Droppo, James G.

2006-07-01

The Department of Homeland Security and others rely on results from atmospheric dispersion models for threat evaluation, event management, and post-event analyses. The ability to simulate dry deposition rates is a crucial part of our emergency preparedness capabilities. Deposited materials pose potential hazards from radioactive shine, inhalation, and ingestion pathways. A reliable characterization of these potential exposures is critical for management and mitigation of these hazards. A review of the current status of dry deposition formulations used in these atmospheric dispersion models was conducted. The formulations for dry deposition of particulate materials from am event such as a radiological attack involving a Radiological Detonation Device (RDD) is considered. The results of this effort are applicable to current emergency preparedness capabilities such as are deployed in the Interagency Modeling and Atmospheric Assessment Center (IMAAC), other similar national/regional emergency response systems, and standalone emergency response models. The review concludes that dry deposition formulations need to consider the full range of particle sizes including: 1) the accumulation mode range (0.1 to 1 micron diameter) and its minimum in deposition velocity, 2) smaller particles (less than .01 micron diameter) deposited mainly by molecular diffusion, 3) 10 to 50 micron diameter particles deposited mainly by impaction and gravitational settling, and 4) larger particles (greater than 100 micron diameter) deposited mainly by gravitational settling. The effects of the local turbulence intensity, particle characteristics, and surface element properties must also be addressed in the formulations. Specific areas for improvements in the dry deposition formulations are 1) capability of simulating near-field dry deposition patterns, 2) capability of addressing the full range of potential particle properties, 3) incorporation of particle surface retention/rebound processes, and

Toward Synchronous Evaluation of Source Apportionments for Atmospheric Concentration and Deposition of Sulfate Aerosol Over East Asia

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Itahashi, S.

2018-03-01

Source apportionments for atmospheric concentration, dry deposition, and wet deposition of sulfate aerosol (SO42-) were synchronously evaluated over East Asia, a main source of anthropogenic sulfur dioxide (SO2) emissions. Estimating dry deposition was difficult owing to the difficulty of measuring deposition velocity directly; therefore, sensitivity simulations using two dry deposition schemes were conducted. Moreover, sensitivity simulations for different emission inventories, the largest uncertainty source in the air quality model, were also conducted. In total, four experimental settings were used. Model performance was verified for atmospheric concentration and wet deposition using a ground-based observation network in China, Korea, and Japan, and all four model settings captured the observations. The underestimation of wet deposition over China was improved by an adjusted approach that linearly scaled the modeled precipitation values to observations. The synchronous evaluation of source apportionments for atmospheric concentration and dry and wet deposition showed the dominant contribution of anthropogenic emissions from China to the atmospheric concentration and deposition in Japan. The contributions of emissions from volcanoes were more important for wet deposition than for atmospheric concentration. Differences in the dry deposition scheme and emission inventory did not substantially influence the relative ratio of source apportionments over Japan. Because the dry deposition was more attributed to local factors, the differences in dry deposition may be an important determinant of the source contributions from China to Japan. Verification of these findings, including the dry deposition velocity, is necessary for better understanding of the behavior of sulfur compound in East Asia.

Organic micropollutants in wet and dry depositions in the Venice Lagoon.

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Gambaro, Andrea; Radaelli, Marta; Piazza, Rossano; Stortini, Angela Maria; Contini, Daniele; Belosi, Franco; Zangrando, Roberta; Cescon, Paolo

2009-08-01

Atmospheric transport is an important route by which pollutants are conveyed from the continents to both coastal and open sea. The role of aerosol deposition in the transport of polycyclic aromatic hydrocarbons (PAHs), polychlorobiphenyls (PCBs) and polybromodiphenyls ethers (PBDEs) to water and soil systems has been evaluated by measuring their concentrations in wet and dry depositions to the Venice Lagoon. The organic micropollutant flux data indicate that they contribute to the total deposition flux in different ways through wet and dry deposition, showing that the prevalent contribution derives from wet deposition. The fluxes calculated for PBDEs, showed the prevalence of 47, 99, 100 and 183 congeners, both in dry and wet fluxes. With regard to PCBs, the flux of summation operatorPCB for wet deposition is in the same order of magnitude of the diffusive flux at the air-water interface. The PAH fluxes obtained in the present study are similar to those obtained in previous studies on the atmospheric bulk deposition to the Venice Lagoon. The ratios between Phe/Ant and Fl/Py indicate that the pollutants sources are pyrolytic, deriving from combustion fuels.

Atmospheric dry deposition in the vicinity of the Salton Sea, California - I: Air pollution and deposition in a desert environment

Science.gov (United States)

Alonso, R.; Bytnerowicz, A.; Boarman, W.I.

2005-01-01

Air pollutant concentrations and atmospheric dry deposition were monitored seasonally at the Salton Sea, southern California. Measurements of ozone (O 3), nitric acid vapor (HNO3), ammonia (NH3), nitric oxide (NO), nitrogen dioxide (NO2) and sulfur dioxide (SO 2) were performed using passive samplers. Deposition rates of NO 3-, NH4+, Cl-, SO 42-, Na+, K+ and Ca2+ to creosote bush branches and nylon filters as surrogate surfaces were determined for one-week long exposure periods. Maximum O3 values were recorded in spring with 24-h average values of 108.8 ??g m-3. Concentrations of NO and NO2 were low and within ranges of the non-urban areas in California (0.4-5.6 and 3.3-16.2 ??g m-3 ranges, respectively). Concentrations of HNO3 (2.0-6.7 ??g m-3) and NH 3 (6.4-15.7 ??g m-3) were elevated and above the levels typical for remote locations in California. Deposition rates of Cl-, SO42-, Na+, K+ and Ca2+ were related to the influence of sea spray or to suspended soil particles, and no strong enrichments caused by ions originated by human activities were detected. Dry deposition rates of NO3- and NH4+ were similar to values registered in areas where symptoms of nitrogen saturation and changes in species composition have been described. Deposition of nitrogenous compounds might be contributing to eutrophication processes at the Salton Sea. ?? 2005 Elsevier Ltd. All rights reserved.

Dry Deposition of Polycyclic Aromatic Hydrocarbons (PAHs) at a Suburban Site in Beijing, China

Science.gov (United States)

Zhang, Xincheng; Wang, Weiyu; Zhu, Xianlei

2017-04-01

A great amount of polycyclic aromatic hydrocarbons (PAHs) have been generated by industrial production, waste incineration and landfill, traffic and road dust etc. They are emitted into atmosphere and afterwards enter into water body and soil through deposition, resulting in wide distribution of PAHs in environment. However, the dry deposition of PAHs from atmosphere has not been well studied, especially in the aspects of its characteristics, environmental and health effects, sources and mechanism. This study measured PAHs dry deposition in the northwest suburban area of Beijing. Dry deposition samples (i.e. dustfall samples) were collected at the sampling site located in China University of Petroleum - Beijing in 2012-2016. And PAHs in the samples were determined by GC/MS. The dry deposition flux of 16 US EPA priority PAHs (ΣPAH16) was 2.58 μg/(m^2·d), which was lower than those in other regions of North China. Its seasonal variability was more significant than annual variability (p spring > autumn > summer. The amount of ΣPAH16 removed from the atmosphere by dry deposition process accounted for only 1.2% of their emissions, indicating that the atmosphere self-purification capacity was quite limited and emission reduction measures would play a key role in controlling PAHs air pollution. However, PAHs dry deposition would deteriorate soil quality since the content of ΣPAH16 in dustfall was 1-2 orders of magnitude higher than that in soil in the same area. Dermal exposure resulting from PAHs dry deposition was not the major route. The sources of PAHs dry deposition varied with seasons. The profile and specific ratios of PAHs showed that in winter, domestic coal combustion was the main source of PAHs with the contribution up to 77%; in spring and summer, the impact of coal combustion decreased and the contribution of vehicle exhaust increased to 30% - 45%; in fall, in addition to coal combustion and vehicle exhaust, the impact of biomass burning was observed

Evaluation of five dry particle deposition parameterizations for incorporation into atmospheric transport models

Science.gov (United States)

Khan, Tanvir R.; Perlinger, Judith A.

2017-10-01

Despite considerable effort to develop mechanistic dry particle deposition parameterizations for atmospheric transport models, current knowledge has been inadequate to propose quantitative measures of the relative performance of available parameterizations. In this study, we evaluated the performance of five dry particle deposition parameterizations developed by Zhang et al. (2001) (Z01), Petroff and Zhang (2010) (PZ10), Kouznetsov and Sofiev (2012) (KS12), Zhang and He (2014) (ZH14), and Zhang and Shao (2014) (ZS14), respectively. The evaluation was performed in three dimensions: model ability to reproduce observed deposition velocities, Vd (accuracy); the influence of imprecision in input parameter values on the modeled Vd (uncertainty); and identification of the most influential parameter(s) (sensitivity). The accuracy of the modeled Vd was evaluated using observations obtained from five land use categories (LUCs): grass, coniferous and deciduous forests, natural water, and ice/snow. To ascertain the uncertainty in modeled Vd, and quantify the influence of imprecision in key model input parameters, a Monte Carlo uncertainty analysis was performed. The Sobol' sensitivity analysis was conducted with the objective to determine the parameter ranking from the most to the least influential. Comparing the normalized mean bias factors (indicators of accuracy), we find that the ZH14 parameterization is the most accurate for all LUCs except for coniferous forest, for which it is second most accurate. From Monte Carlo simulations, the estimated mean normalized uncertainties in the modeled Vd obtained for seven particle sizes (ranging from 0.005 to 2.5 µm) for the five LUCs are 17, 12, 13, 16, and 27 % for the Z01, PZ10, KS12, ZH14, and ZS14 parameterizations, respectively. From the Sobol' sensitivity results, we suggest that the parameter rankings vary by particle size and LUC for a given parameterization. Overall, for dp = 0.001 to 1.0 µm, friction velocity was one of

Dispersion, deposition and resuspension of atmospheric contaminants

International Nuclear Information System (INIS)

Anon.

1985-01-01

The following topics are discussed: dry deposition, oil shale fugitive air emissions, particle resuspension and translocation, theoretical studies and applications, and processing of emissions by clouds and precipitation. The concentration of contaminant species in air is governed by the rate of input from sources, the rate of dilution or dispersion as a result of air turbulence, and the rate of removal to the surface by wet and dry deposition processes. Once on the surface, contaminants also may be resuspended, depending on meteorological and surface conditions. An understanding of these processes is necessary for accurate prediction of exposures of hazardous or harmful contaminants to humans, animals, and crops. In the field, plume dispersion and plume depletion by dry deposition were studied by the use of tracers. Dry deposition was investigated for particles of both respiration and inhalation interest. Complementary dry deposition studies of particles to rock canopies were conducted under controlled conditions in a wind tunnel. Because of increasing concern about hazardous, organic gases in the atmosphere some limited investigations of the dry deposition of nitrobenzene to a lichen mat were conducted in a stirred chamber. Resuspension was also studied using tracers and contaminated surfaces and in the wind tunnel. The objective of the resuspension studies was to develop and verify models for predicting the airborne concentrations of contaminants over areas with surface contamination, develop resuspension rate predictors for downwind transport, and develop predictors for resuspension input to the food chain. These models will be of particular relevance to the evaluation of deposition and resuspension of both radionuclides and chemical contaminants

Atmospheric deposition of polycyclic aromatic hydrocarbons (PAHs) in Shanghai: the spatio-temporal variation and source identification

Science.gov (United States)

Cheng, Chen; Bi, Chunjuan; Wang, Dongqi; Yu, Zhongjie; Chen, Zhenlou

2018-03-01

This study investigated the dry and wet deposition fluxes of atmospheric polycyclic aromatic hydrocarbons (PAHs) in Shanghai, China. The flux sources were traced based on composition and spatio-temporal variation. The results show that wet deposition concentrations of PAHs ranged from 0.07 to 0.67 mg·L-1 and were correlated with temperature ( P<0.05). Dry deposition of PAHs concentrations ranged from 3.60-92.15 mg·L-1 and were higher in winter and spring than in summer and autumn. The annual PAH average fluxes were 0.631 mg·m-2·d-1 and 4.06 mg·m-2·d-1 for wet and dry deposition, respectively. The highest wet deposition of PAH fluxes was observed in summer, while dry deposition fluxes were higher in winter and spring. Atmospheric PAHs were deposited as dry deposition in spring and winter, yet wet deposition was the dominant pathway during summer. Total atmospheric PAH fluxes were higher in the northern areas than in the southern areas of Shanghai, and were also observed to be higher in winter and spring. Annual deposition of atmospheric PAHs was about 10.8 t in across all of Shanghai. Wet deposition of PAHs was primarily composed of two, three, or four rings, while dry deposition of PAHs was composed of four, five, or six rings. The atmospheric PAHs, composed of four, five, or six rings, primarily existed in the form of particulates. Coal combustion and vehicle emissions were the dominant sources of PAH in the observed area of downtown Shanghai. In suburban areas, industrial pollution, from sources such as coke oven, incinerator, and oil fired power plant, was as significant as vehicle emissions in contributing to the deposition of PAHs.

Characterization of Wet and Dry Deposition in the Downwind of Industrial Sources in a Dry Tropical Area

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Raj K. Singh

2001-01-01

Full Text Available An atmospheric deposition study was conducted in the downwind of Shaktinagar Thermal Power Plant (STPP, Renusagar Thermal Power Plant (RTPP, and Anpara Thermal Power Plant (ATPP, at Singrauli region, Uttar Pradesh (UP, India to characterize dry and wet deposition in relation to different pollution loading. During the study period, dry and wet depositions and levels of gaseous pollutants (SO2 and NO2 were estimated across the sites. Dry deposition was collected on a monthly basis and wet deposition on an event basis. Depositions were analyzed for pH, nitrate (NO3�, ammonium (NH4+, and sulphate (SO42� contents. Dry deposition rate both collected as clearfall and throughfall varied between 0.15 to 2.28 and 0.33 to 3.48 g m�2 day�1, respectively, at control and maximally polluted sites. The pH of dry deposition varied from 5.81 to 6.89 during winter and 6.09 to 7.02 during summer across the sites. During the rainy season, the mean pH of clear wet deposition varied from 6.56 to 7.04 and throughfall varied from 6.81 to 7.22. The concentrations of NO2 and SO2 pollutants were highest during the winter season. Mean SO2 concentrations varied from 18 to 75 �g m�3 at control and differently polluted sites during the winter season. The variation in NO2 concentrations did not show a pattern similar to that of SO2. The highest NO2 concentration during the winter season was 50 �g m�3, observed near RTPP. NO2 concentration did not show much variation among different sites, suggesting that the sources of NO2 emission are evenly distributed along the sites. The concentrations of NH4+, NO3�, and SO42� ions in dry deposition were found to be higher in summer as compared to the winter season. In dry deposition (clearfall the concentrations of NH4+, NO3�, and SO42� varied from 0.13 to 1.0, 0.81 to 1.95, and 0.82 to 3.27 mg l�1, respectively, during winter. In wet deposition (clearfall, the above varied from 0.14 to 0.74, 0.81 to 1.82, and 0

Characterization of wet and dry deposition in the downwind of industrial sources in a dry tropical area.

Science.gov (United States)

Singh, R K; Agrawal, M

2001-12-19

An atmospheric deposition study was conducted in the downwind of Shaktinagar Thermal Power Plant (STPP), Renusagar Thermal Power Plant (RTPP), and Anpara Thermal Power Plant (ATPP), at Singrauli region, Uttar Pradesh (UP), India to characterize dry and wet deposition in relation to different pollution loading. During the study period, dry and wet depositions and levels of gaseous pollutants (SO2 and NO2) were estimated across the sites. Dry deposition was collected on a monthly basis and wet deposition on an event basis. Depositions were analyzed for pH, nitrate (NO3-), ammonium (NH4+), and sulphate (SO4(2-)) contents. Dry deposition rate both collected as clearfall and throughfall varied between 0.15 to 2.28 and 0.33 to 3.48 g m(-2) day(-1), respectively, at control and maximally polluted sites. The pH of dry deposition varied from 5.81 to 6.89 during winter and 6.09 to 7.02 during summer across the sites. During the rainy season, the mean pH of clear wet deposition varied from 6.56 to 7.04 and throughfall varied from 6.81 to 7.22. The concentrations of NO2 and SO2 pollutants were highest during the winter season. Mean SO2 concentrations varied from 18 to 75 g m(-3) at control and differently polluted sites during the winter season. The variation in NO2 concentrations did not show a pattern similar to that of SO2. The highest NO2 concentration during the winter season was 50 g m(-3), observed near RTPP. NO2 concentration did not show much variation among different sites, suggesting that the sources of NO2 emission are evenly distributed along the sites. The concentrations of NH4+, NO3-, and SO4(2-) ions in dry deposition were found to be higher in summer as compared to the winter season. In dry deposition (clearfall) the concentrations of NH4+, NO3-, and SO4(2-) varied from 0.13 to 1.0, 0.81 to 1.95, and 0.82 to 3.27 mg l(-1), respectively, during winter. In wet deposition (clearfall), the above varied from 0.14 to 0.74, 0.81 to 1.82, and 0.67 to 2.70 mg l(-1

Microstructure of oxides in thermal barrier coatings grown under dry/humid atmosphere

International Nuclear Information System (INIS)

Zhou Zhaohui; Guo Hongbo; Wang Juan; Abbas, Musharaf; Gong Shengkai

2011-01-01

Graphical abstract: The presence of water vapor promoted the formation of spinels in the TBC. Highlights: → Thermal barrier coatings are produced by electron beam physical vapour deposition. → Oxidation behaviour of the coatings at 1100 deg. C has been investigated in dry/humid O 2 . → Thermally grown oxides formed in the coatings are characterized. → The presence of water vapour promotes the formation of spinel in the TBCs. - Abstract: The microstructure of thermally grown oxide (TGO) in thermal barrier coatings (TBCs) oxidized under dry/humid atmosphere at 1100 deg. C has been characterized by transmission electron microscopy. A thin and continuous oxide layer is formed in the as-deposited TBCs produced by electron beam physical vapor deposition. The TGO formed in dry atmosphere consists of an outer layer of fine α-alumina, zirconia grains and an inner layer of columnar α-alumina grains. However, a small amount of spinel is observed in the TGO under humid atmosphere. The presence of water vapour promotes the formation of spinel.

Dry deposition of polychlorinated biphenyls in urban areas

International Nuclear Information System (INIS)

Holsen, T.M.; Noll, K.E.; Shiping Liu, Wenjhy Lee

1991-01-01

The PCB dry deposition flux was measured in Chicago with a greased, Mylar-covered smooth plate with a sharp leading edge pointed into the wind. The dry deposition flux of PCBs in Chicago averaged 3.8 μg/m 2 ·day between May and November 1989 and 6.0 μg/m 2 ·day for May and June 1990. A comparison of the PCB flux measured in Chicago to an estimated nonurban PCB flux shows that the flux of PCBs is up to 3 orders of magnitude higher in urban areas than in nonurban areas, indicating that Chicago and other urban areas near the Great Lakes must be considered as major source terms for deposition of PCBs into the lakes. The distribution of atmospheric PCBs between the gas and particle phase and the size distribution of particle-phase PCBs were also measured. The airborne PCB concentration as measured by the Noll rotary impactor (NRI) A stage (particles with aerodynamic diameters of > 6.5 μm) was higher in Chicago (0.94 ng/m 3 ) than in Los Angeles (0.52 ng/m 3 ), as was the mean particle-phase PCB concentration (47 vs 21 μg/g). PCBs were found to be associated with all sizes of atmospheric particles; however, their particle mass normalized concentration decreased with increasing particle size. PCBs associated with particles, particularly coarse particles, represented a significant fraction of the total PCB dry deposition flux even though PCBs in the ambient air were present primarily in the gas phase

Field measurements of the atmospheric dry deposition fluxes and velocities of polycyclic aromatic hydrocarbons to the global oceans.

Science.gov (United States)

González-Gaya, Belén; Zúñiga-Rival, Javier; Ojeda, María-José; Jiménez, Begoña; Dachs, Jordi

2014-05-20

The atmospheric dry deposition fluxes of 16 polycyclic aromatic hydrocarbons (PAHs) have been measured, for the first time, in the tropical and subtropical Atlantic, Pacific, and Indian Oceans. Depositional fluxes for fine (0.7-2.7 μm) and coarse (>2.7 μm) aerosol fractions were simultaneously determined with the suspended aerosol phase concentrations, allowing the determination of PAH deposition velocities (vD). PAH dry deposition fluxes (FDD) bound to coarse aerosols were higher than those of fine aerosols for 83% of the measurements. Average FDD for total (fine + coarse) Σ16PAHs (sum of 16 individual PAHs) ranged from 8.33 ng m(-2)d(-1) to 52.38 ng m(-2)d(-1). Mean FDD for coarse aerosol's individual PAHs ranged between 0.13 ng m(-2)d(-1) (Perylene) and 1.96 ng m(-2)d(-1) (Methyl Pyrene), and for the fine aerosol fraction these ranged between 0.06 ng m(-2)d(-1) (Dimethyl Pyrene) and 1.25 ng m(-2)d(-1) (Methyl Chrysene). The estimated deposition velocities went from the highest mean vD for Methyl Chrysene (0.17-13.30 cm s(-1)), followed by Dibenzo(ah)Anthracene (0.29-1.38 cm s(-1)), and other high MW PAHs to minimum values of vD for Dimethyl Pyrene (oceans.

A MULTILAYER BIOCHEMICAL DRY DEPOSITION MODEL 1. MODEL FORMULATION

Science.gov (United States)

A multilayer biochemical dry deposition model has been developed based on the NOAA Multilayer Model (MLM) to study gaseous exchanges between the soil, plants, and the atmosphere. Most of the parameterizations and submodels have been updated or replaced. The numerical integration ...

Evaluation of five dry particle deposition parameterizations for incorporation into atmospheric transport models

Directory of Open Access Journals (Sweden)

T. R. Khan

2017-10-01

Full Text Available Despite considerable effort to develop mechanistic dry particle deposition parameterizations for atmospheric transport models, current knowledge has been inadequate to propose quantitative measures of the relative performance of available parameterizations. In this study, we evaluated the performance of five dry particle deposition parameterizations developed by Zhang et al. (2001 (Z01, Petroff and Zhang (2010 (PZ10, Kouznetsov and Sofiev (2012 (KS12, Zhang and He (2014 (ZH14, and Zhang and Shao (2014 (ZS14, respectively. The evaluation was performed in three dimensions: model ability to reproduce observed deposition velocities, Vd (accuracy; the influence of imprecision in input parameter values on the modeled Vd (uncertainty; and identification of the most influential parameter(s (sensitivity. The accuracy of the modeled Vd was evaluated using observations obtained from five land use categories (LUCs: grass, coniferous and deciduous forests, natural water, and ice/snow. To ascertain the uncertainty in modeled Vd, and quantify the influence of imprecision in key model input parameters, a Monte Carlo uncertainty analysis was performed. The Sobol' sensitivity analysis was conducted with the objective to determine the parameter ranking from the most to the least influential. Comparing the normalized mean bias factors (indicators of accuracy, we find that the ZH14 parameterization is the most accurate for all LUCs except for coniferous forest, for which it is second most accurate. From Monte Carlo simulations, the estimated mean normalized uncertainties in the modeled Vd obtained for seven particle sizes (ranging from 0.005 to 2.5 µm for the five LUCs are 17, 12, 13, 16, and 27 % for the Z01, PZ10, KS12, ZH14, and ZS14 parameterizations, respectively. From the Sobol' sensitivity results, we suggest that the parameter rankings vary by particle size and LUC for a given parameterization. Overall, for dp  =  0.001 to 1.0�

Occurrence and dry deposition of organophosphate esters in atmospheric particles over the northern South China Sea.

Science.gov (United States)

Lai, Senchao; Xie, Zhiyong; Song, Tianli; Tang, Jianhui; Zhang, Yingyi; Mi, Wenying; Peng, Jinhu; Zhao, Yan; Zou, Shichun; Ebinghaus, Ralf

2015-05-01

Nine organophosphate esters (OPEs) in airborne particles were measured during a cruise campaign over the northern South China Sea (SCS) from September to October 2013. The concentration of the total OPEs (∑OPEs) was 47.1-160.9 pg m(-3), which are lower than previous measurements in marine atmosphere environments. Higher OPE concentrations were observed in terrestrially influenced samples, suggesting that OPE concentrations were significantly influenced by air mass transport. Chlorinated OPEs were the dominant OPEs, accounting for 65.8-83.7% of the ∑OPEs. Tris-(2-chloroethyl) phosphate (TCEP) was the predominant OPE compound in the samples (45.0±12.1%), followed by tris-(1-chloro-2-propyl) phosphates (TCPPs) (28.8±8.9%). Dry particle-bound deposition fluxes ranged from 8.2 to 27.8 ng m(-2) d(-1) for the ∑OPEs. Moreover, the dry deposition input of the ∑OPEs was estimated to be 4.98 ton y(-1) in 2013 in a vast area of northern SCS. About half of the input was found to relate to air masses originating from China. Copyright © 2015 Elsevier Ltd. All rights reserved.

Atmospheric transport, diffusion, and deposition of radioactivity

International Nuclear Information System (INIS)

Crawford, T.V.

1969-01-01

From a meteorological standpoint there are two types of initial sources for atmospheric diffusion from Plowshare applications. One is the continuous point-source plume - a slow, small leak from an underground engineering application. The other is the large cloud produced almost instantaneously from a cratering application. For the purposes of this paper the effluent from neither type has significant fall speed. Both are carried by the prevailing wind, but the statistics of diffusion for each type are different. The use of constant altitude, isobaric and isentropic techniques for predicting the mean path of the effluent is briefly discussed. Limited data are used to assess the accuracy of current trajectory forecast techniques. Diffusion of continuous point-source plumes has been widely studied; only a brief review is given of the technique used and the variability of their results with wind speed and atmospheric stability. A numerical model is presented for computing the diffusion of the 'instantaneously-produced' large clouds. This model accounts for vertical and diurnal changes in atmospheric turbulence, wet and dry deposition, and radioactivity decay. Airborne concentrations, cloud size, and deposition on the ground are calculated. Pre- and post-shot calculations of cloud center, ground level concentration of gross radioactivity, and dry and wet deposition of iodine-131 are compared with measurements on Cabriolet and Buggy. (author)

Atmospheric transport, diffusion, and deposition of radioactivity

Energy Technology Data Exchange (ETDEWEB)

Crawford, T V [Lawrence Radiation Laboratory, Livermore, CA (United States)

1969-07-01

From a meteorological standpoint there are two types of initial sources for atmospheric diffusion from Plowshare applications. One is the continuous point-source plume - a slow, small leak from an underground engineering application. The other is the large cloud produced almost instantaneously from a cratering application. For the purposes of this paper the effluent from neither type has significant fall speed. Both are carried by the prevailing wind, but the statistics of diffusion for each type are different. The use of constant altitude, isobaric and isentropic techniques for predicting the mean path of the effluent is briefly discussed. Limited data are used to assess the accuracy of current trajectory forecast techniques. Diffusion of continuous point-source plumes has been widely studied; only a brief review is given of the technique used and the variability of their results with wind speed and atmospheric stability. A numerical model is presented for computing the diffusion of the 'instantaneously-produced' large clouds. This model accounts for vertical and diurnal changes in atmospheric turbulence, wet and dry deposition, and radioactivity decay. Airborne concentrations, cloud size, and deposition on the ground are calculated. Pre- and post-shot calculations of cloud center, ground level concentration of gross radioactivity, and dry and wet deposition of iodine-131 are compared with measurements on Cabriolet and Buggy. (author)

Deposition to forests in Europe: most important factors influencing dry deposition and models used for generalisation

International Nuclear Information System (INIS)

Erisman, Jan Willem; Draaijers, Geert

2003-01-01

The influence of forest characteristics on deposition can be modelled reasonably well; forest edge effects and dynamical processes are still uncertain. - Dry deposition of gases and particles to forests is influenced by factors influencing the turbulent transport, such as wind speed, tree height, canopy closure, LAI, etc. as well as by factors influencing surface condition, such as precipitation, relative humidity, global radiation, etc. In this paper, an overview of these factors is given and it is shown which are the most important determining temporal and spatial variation of dry deposition of sodium and sulphur. Furthermore, it is evaluated how well current deposition models are able to describe the temporal and spatial variation in dry deposition. It is concluded that the temporal variation is not modelled well enough, because of limited surface-wetness exchange parameterisations. The influence of forest characteristics are modelled reasonably well, provided enough data describing the forests and the spatial variation in concentration is available. For Europe these data are not available. The means to decrease the atmospheric deposition through forest management is discussed

Lichen-based critical loads for atmospheric nitrogen deposition in Western Oregon and Washington forests, USA

Science.gov (United States)

Linda H. Geiser; Sarah E. Jovan; Doug A. Glavich; Matthew K. Porter

2010-01-01

Critical loads (CLs) define maximum atmospheric deposition levels apparently preventative of ecosystem harm. We present first nitrogen CLs for northwestern North America's maritime forests. Using multiple linear regression, we related epiphytic-macrolichen community composition to: 1) wet deposition from the National Atmospheric Deposition Program, 2) wet, dry,...

Effect of Ground Surface Roughness on Atmospheric Dispersion and Dry Deposition of Cs-137 in the UAE Environment

Energy Technology Data Exchange (ETDEWEB)

Kim, Sungyeop; Beeley, Philip A. [Khalifa Univ. of Science, Abu Dhabi (United Arab Emirates); Kim, Sungyeop; Chang, Soonheung; Lee, Kunjai [Korea Advanced Institute of Science and Technology, Daejeon (Korea, Republic of)

2013-05-15

The site of nuclear power plant (NPP) in the UAE has several unique characteristics as a NPP on the desert environment near coastal region. Those characteristics are represented like below: · Arid ground surface · Low ground surface roughness length · Relatively simple (flat) terrain · Extremely low precipitation · Intense solar radiation and high temperature in day time · Sea breeze · Relatively high humidity of atmosphere · Etc. From the review of this desert environment in the UAE, low ground surface roughness is regarded as one of definitively different characteristics from that of other NPP sites. In this context, surface roughness is selected as independent variables for the sensitivity analyses in this research. Another important reason of this selection is that this parameters is less dependent on the day and night change than other parameters. With ground level concentration, dry deposition rate has been chosen as a dependent variable to be considered rather than wet deposition because UAE shows almost zero rainfall especially in summer. Lower ground level concentration of Cs-137 near the site and extremely lower dry deposition of Cs-137 are predicted in the UAE environment because of the lower ground surface roughness of the desert.

Observation- and model-based estimates of particulate dry nitrogen deposition to the oceans

Directory of Open Access Journals (Sweden)

A. R. Baker

2017-07-01

Full Text Available Anthropogenic nitrogen (N emissions to the atmosphere have increased significantly the deposition of nitrate (NO3− and ammonium (NH4+ to the surface waters of the open ocean, with potential impacts on marine productivity and the global carbon cycle. Global-scale understanding of the impacts of N deposition to the oceans is reliant on our ability to produce and validate models of nitrogen emission, atmospheric chemistry, transport and deposition. In this work,  ∼  2900 observations of aerosol NO3− and NH4+ concentrations, acquired from sampling aboard ships in the period 1995–2012, are used to assess the performance of modelled N concentration and deposition fields over the remote ocean. Three ocean regions (the eastern tropical North Atlantic, the northern Indian Ocean and northwest Pacific were selected, in which the density and distribution of observational data were considered sufficient to provide effective comparison to model products. All of these study regions are affected by transport and deposition of mineral dust, which alters the deposition of N, due to uptake of nitrogen oxides (NOx on mineral surfaces. Assessment of the impacts of atmospheric N deposition on the ocean requires atmospheric chemical transport models to report deposition fluxes; however, these fluxes cannot be measured over the ocean. Modelling studies such as the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP, which only report deposition flux, are therefore very difficult to validate for dry deposition. Here, the available observational data were averaged over a 5° × 5° grid and compared to ACCMIP dry deposition fluxes (ModDep of oxidised N (NOy and reduced N (NHx and to the following parameters from the Tracer Model 4 of the Environmental Chemical Processes Laboratory (TM4: ModDep for NOy, NHx and particulate NO3− and NH4+, and surface-level particulate NO3− and NH4+ concentrations. As a model ensemble, ACCMIP can be

Effects of geographical location and land use on atmospheric deposition of nitrogen in the State of Connecticut

International Nuclear Information System (INIS)

Luo, Yuzhou; Yang, Xiusheng; Carley, Robert J.; Perkins, Christopher

2003-01-01

High ambient concentrations of tropospheric nitrogen and dry deposition flux were found in urban areas. - A network of eight monitoring stations was established to study the atmospheric nitrogen concentration and deposition in the State of Connecticut. The stations were classified into urban, rural, coastal and inland categories to represent the geographical location and land use characteristics surrounding the monitoring sites. Nitrogen species including nitrate, ammonium, nitric acid vapor and organic nitrogen in the air and precipitation were collected, analyzed and used to infer nitrogen concentrations and dry and wet deposition flux densities for the sampling period from 1997 through 1999, with independently collected meteorological data. Statistical analyses were conducted to evaluate the spatial variations of atmospheric concentration and deposition fluxes of total nitrogen in Connecticut. A slightly higher atmospheric concentration of total nitrogen was observed along the Connecticut coastline of Long Island Sound compared to inland areas, while the differences of nitrogen deposition fluxes were insignificant between coastal and inland sites. The land use characteristics surrounding the monitoring sites had profound effects on the atmospheric nitrogen concentration and dry deposition flux. The ambient nitrogen concentration over the four urban sites was averaged 38.9% higher than that over the rural sites, resulting a 58.0% higher dry deposition flux in these sites compared to their rural counterparts. The local industrial activities and traffic emissions of nitrogen at urban areas had significant effects on the spatial distribution of atmospheric nitrogen concentration and dry deposition flux in the State. Wet and total deposition fluxes appeared to be invariant between the monitoring sites, except for high flux densities measured at Old Greenwich, a monitoring station near to and downwind of the New York and New Jersey industrial complexes

The sources of trace element pollution of dry depositions nearby a drinking water source.

Science.gov (United States)

Guo, Xinyue; Ji, Hongbing; Li, Cai; Gao, Yang; Ding, Huaijian; Tang, Lei; Feng, Jinguo

2017-02-01

Miyun Reservoir is one of the most important drinking water sources for Beijing. Thirteen atmospheric PM sampling sites were established around this reservoir to analyze the mineral composition, morphological characteristics, element concentration, and sources of atmospheric PM pollution, using transmission electron microscope, X-ray diffraction, and inductively coupled plasma mass spectrometry analyses. The average monthly dry deposition flux of aerosols was 15.18 g/m 2 , with a range of 5.78-47.56 g/m 2 . The maximum flux season was winter, followed by summer, autumn, and spring. Zn and Pb pollution in this area was serious, and some of the sample sites had Cr, Co, Ni, and Cu pollution. Deposition fluxes of Zn/Pb in winter and summer reached 99.77/143.63 and 17.04/33.23 g/(hm 2 month), respectively. Principal component analysis showed two main components in the dry deposition; the first was Cr, Co, Ni, Cu, and Zn, and the other was Pb and Cd. Principal sources of the trace elements were iron mining and other anthropogenic activities in the surrounding areas and mountainous area north of the reservoir. Mineralogy analysis and microscopic conformation results showed many iron minerals and some unweathered minerals in dry deposition and atmospheric particulate matter, which came from an iron ore yard in the northern mountainous area of Miyun County. There was possible iron-rich dry deposition into Miyun Reservoir, affecting its water quality and harming the health of people living in areas around the reservoir and Beijing.

Recent field studies of dry deposition to surfaces in plant canopies

International Nuclear Information System (INIS)

Lindberg, S.E.; Lovett, G.M.; Bondietti, E.A.; Davidson, C.I.

1984-01-01

A variety of field techniques were used to assess the dry deposition of sulfur. In a deciduous forest canopy in eastern Tennessee, inert petri plates and adjacent chestnut oak leaves showed similar SO 4 -2 deposition velocities of about 0.1 cm s -1 . In the same forest, statistical analysis of throughfall yielded a deposition velocity of 0.48 cm s -1 for total sulfur (SO 4 -2 plus SO 2 ). The throughfall technique appears useful for scaling individual surface measurements to larger spatial and temporal scales. On a grassy field in Illinois, flat Teflon plates, petri dishes, and dustfall buckets were exposed side by side. Measured sulfate deposition increased with increasing rim height on the collection surface, and deposition velocities ranged from 0.14 to 0.70 cm s -1 . Much of the deposition to these surfaces can be attributed to large-particle SO 4 -2 . Dry season (summer) deposition velocities of 7 Be in California were found to be similar to dry deposition velocities of 212 Pb in Tennessee, ranging from 0.18 to 0.35 cm s -1 . These natural radionuclides attach to submicron aerosols in the atmosphere and may be useful tracers of submicron SO 4 -2 deposition. 9 references, 5 figures, 4 tables

Atmospheric heavy metal deposition in the Copenhagen area

DEFF Research Database (Denmark)

Andersen, Allan; Hovmand, Mads Frederik; Johnsen, Ib

1978-01-01

Atmospheric dry and wet deposition (bulk precipitation) of the heavy metals Cu, Pb, Zn, Ni, V and Fe over the Copenhagen area was measured by sampling in plastic funnels from 17 stations during a twelve-month period. Epigeic bryophytes from 100 stations in the area were analysed for the heavy...

Phenomenological study of aerosol dry deposition in urban area: surface properties, turbulence and local meteorology influences

International Nuclear Information System (INIS)

Roupsard, P.

2013-01-01

Aerosol dry deposition is not much known for urban areas due to the lack of data. Knowledge on this phenomenon is necessary to understand pollutant fluxes in cities and to estimate inhabitant exposition to ionizing radiation of radioactive aerosols. A data providing could enable to enhance dry deposition models for these areas. An original experimental approach is performed to study submicron aerosol dry deposition on urban surfaces. Wind tunnel coupled to in situ experiments give results to study different physical phenomenon governing dry deposition. Dry deposition velocities are measured using aerosol tracers. These data are associated to turbulent and meteorological measured conditions. This database permits to classify the principal physical phenomenon for each experiment type. Finally, different phenomenon must be considered for chronic and acute exposition of urban surfaces to atmospheric particles. (author)

Atmospheric Deposition of Phosphorus to the Everglades: Concepts, Constraints, and Published Deposition Rates for Ecosystem Management

Directory of Open Access Journals (Sweden)

Garth W. Redfield

2002-01-01

Full Text Available This paper summarizes concepts underlying the atmospheric input of phosphorus (P to ecosystems, published rates of P deposition, measurement methods, and approaches to future monitoring and research. P conveyed through the atmosphere can be a significant nutrient source for some freshwater and marine ecosystems. Particle sources and sinks at the land-air interface produce variation in P deposition from the atmosphere across temporal and spatial scales. Natural plant canopies can affect deposition rates by changing the physical environment and surface area for particle deposition. Land-use patterns can alter P deposition rates by changing particle concentrations in the atmosphere. The vast majority of P in dry atmospheric deposition is conveyed by coarse (2.5 to 10 μm and giant (10 to 100 μm particles, and yet these size fractions represent a challenge for long-term atmospheric monitoring in the absence of accepted methods for routine sampling. Most information on P deposition is from bulk precipitation collectors and wet/dry bucket sampling, both with questionable precision and accuracy. Most published annual rates of P deposition are gross estimates derived from bulk precipitation sampling in locations around the globe and range from about 5 to well over 100 mg P m–2 year–1, although most inland ecosystems receive between 20 and 80 mg P m–2 year–1. Rates below 30 mg P m–2 year–1 are found in remote areas and near coastlines. Intermediate rates of 30 to 50 mg P m–2 year–1 are associated with forests or mixed land use, and rates of 50 to 100 mg P m–2 year–1 or more are often recorded from urban or agricultural settings. Comparison with other methods suggests that these bulk precipitation estimates provide crude boundaries around actual P deposition rates for various land uses. However, data screening cannot remove all positive bias caused by contamination of bucket or bulk collectors. As a consequence, continued sampling

Atmospheric Deposition Modeling Results

Data.gov (United States)

U.S. Environmental Protection Agency — This asset provides data on model results for dry and total deposition of sulfur, nitrogen and base cation species. Components include deposition velocities, dry...

Atmospheric Deposition of Heavy Metals in Soil Affected by Different Soil Uses of Southern Spain

Science.gov (United States)

Acosta, J. A.; Faz, A.; Martínez-Martínez, S.; Bech, J.

2009-04-01

Heavy metals are a natural constituent of rocks, sediments and soils. However, the heavy metal content of top soils is also dependent on other sources than weathering of the indigenous minerals; input from atmospheric deposition seems to be an important pathway. Atmospheric deposition is defined as the process by which atmospheric pollutants are transferred to terrestrial and aquatic surfaces and is commonly classified as either dry or wet. The interest in atmospheric deposition has increased over the past decade due to concerns about the effects of deposited materials on the environment. Dry deposition provides a significant mechanism for the removal of particles from the atmosphere and is an important pathway for the loading of heavy metals into the soil ecosystem. Within the last decade, an intensive effort has been made to determine the atmospheric heavy metal deposition in both urban and rural areas. The main objective of this study was to identification of atmospheric heavy metals deposition in soil affected by different soil uses. Study area is located in Murcia Province (southeast of Spain), in the surroundings of Murcia City. The climate is typically semiarid Mediterranean with an annual average temperature of 18°C and precipitation of 350 mm. In order to determine heavy metals atmospheric deposition a sampling at different depths (0-1 cm, 1-5 cm, 5-15 cm and 15-30 cm) was carried out in 7 sites including agricultural soils, two industrial areas and natural sites. The samples were taken to the laboratory where, dried, passed through a 2 mm sieve, and grinded. For the determination of the moisture the samples were weighed and oven dried at 105 °C for 24 h. The total amounts of metals (Pb, Cu, Pb, Zn, Cd, Mn, Ni and Cr) were determined by digesting the samples with nitric/perchoric acids and measuring with ICP-MS. Results showed that zinc contamination in some samples of industrial areas was detected, even this contamination reaches 30 cm depth; thus it is

Litterfall mercury dry deposition in the eastern USA

International Nuclear Information System (INIS)

Risch, Martin R.; DeWild, John F.; Krabbenhoft, David P.; Kolka, Randall K.; Zhang, Leiming

2012-01-01

Mercury (Hg) in autumn litterfall from predominately deciduous forests was measured in 3 years of samples from 23 Mercury Deposition Network sites in 15 states across the eastern USA. Annual litterfall Hg dry deposition was significantly higher (median 12.3 micrograms per square meter (μg/m 2 ), range 3.5–23.4 μg/m 2 ) than annual Hg wet deposition (median 9.6 μg/m 2 , range 4.4–19.7 μg/m 2 ). The mean ratio of dry to wet Hg deposition was 1.3–1. The sum of dry and wet Hg deposition averaged 21 μg/m 2 per year and 55% was litterfall dry deposition. Methylmercury was a median 0.8% of Hg in litterfall and ranged from 0.6 to 1.5%. Annual litterfall Hg and wet Hg deposition rates differed significantly and were weakly correlated. Litterfall Hg dry deposition differed among forest-cover types. This study demonstrated how annual litterfall Hg dry deposition rates approximate the lower bound of annual Hg dry fluxes. - Highlights: ► Annual litterfall mercury dry deposition was significantly higher than wet deposition. ► The mean ratio of dry to wet mercury deposition was 1.3–1. ► The sum of dry and wet mercury deposition averaged 55% litterfall dry deposition. ► Litterfall mercury deposition was highest in the oak-hickory forest-cover type. ► Methylmercury was a median 0.8% of mercury in litterfall and ranged to 1.5%. - A multi-year study of Mercury Deposition Network sites found that annual mercury dry deposition from litterfall in predominately deciduous forests exceeded annual mercury wet deposition in the eastern USA.

Net atmospheric mercury deposition to Svalbard: Estimates from lacustrine sediments

Science.gov (United States)

Drevnick, Paul E.; Yang, Handong; Lamborg, Carl H.; Rose, Neil L.

2012-11-01

In this study we used lake sediments, which faithfully record Hg inputs, to derive estimates of net atmospheric Hg deposition to Svalbard, Norwegian Arctic. With the exception of one site affected by local pollution, the study lakes show twofold to fivefold increases in sedimentary Hg accumulation since 1850, likely due to long-range atmospheric transport and deposition of anthropogenic Hg. Sedimentary Hg accumulation in these lakes is a linear function of the ratio of catchment area to lake area, and we used this relationship to model net atmospheric Hg flux: preindustrial and modern estimates are 2.5 ± 3.3 μg m-2 y-1 and 7.0 ± 3.0 μg m-2 y-1, respectively. The modern estimate, by comparison with data for Hg wet deposition, indicates that atmospheric mercury depletion events (AMDEs) or other dry deposition processes contribute approximately half (range 0-70%) of the net flux. Hg from AMDEs may be moving in significant quantities into aquatic ecosystems, where it is a concern because of contamination of aquatic food webs.

Dry deposition and soil-air gas exchange of polychlorinated biphenyls (PCBs) in an industrial area.

Science.gov (United States)

Bozlaker, Ayse; Odabasi, Mustafa; Muezzinoglu, Aysen

2008-12-01

Ambient air and dry deposition, and soil samples were collected at the Aliaga industrial site in Izmir, Turkey. Atmospheric total (particle+gas) Sigma(41)-PCB concentrations were higher in summer (3370+/-1617 pg m(-3), average+SD) than in winter (1164+/-618 pg m(-3)), probably due to increased volatilization with temperature. Average particulate Sigma(41)-PCBs dry deposition fluxes were 349+/-183 and 469+/-328 ng m(-2) day(-1) in summer and winter, respectively. Overall average particulate deposition velocity was 5.5+/-3.5 cm s(-1). The spatial distribution of Sigma(41)-PCB soil concentrations (n=48) showed that the iron-steel plants, ship dismantling facilities, refinery and petrochemicals complex are the major sources in the area. Calculated air-soil exchange fluxes indicated that the contaminated soil is a secondary source to the atmosphere for lighter PCBs and as a sink for heavier ones. Comparable magnitude of gas exchange and dry particle deposition fluxes indicated that both mechanisms are equally important for PCB movement between air and soil in Aliaga.

Atmospheric nitrogen deposition budget in a subtropical hydroelectric reservoir (Nam Theun II case study, Lao PDR)

Science.gov (United States)

Adon, Marcellin; Galy-Lacaux, Corinne; Serça, Dominique; Guerin, Frederic; Guedant, Pierre; Vonghamsao, Axay; Rode, Wanidaporn

2016-04-01

With 490 km² at full level of operation, Nam Theun 2 (NT2) is one of the largest hydro-reservoir in South East Asia. NT2 is a trans-basin hydropower project that diverts water from the Nam Theun river (a Mekong tributary) to the Xe Ban Fai river (another Mekong tributary). Atmospheric deposition is an important source of nitrogen (N), and it has been shown that excessive fluxes of N from the atmosphere has resulted in eutrophication of many coastal waters. A large fraction of atmospheric N input is in the form of inorganic N. This study presents an estimation of the atmospheric inorganic nitrogen budget into the NT2 hydroelectric reservoir based on a two-year monitoring (July 2010 to July 2012) including gas concentrations and precipitation. Dry deposition fluxes are calculated from monthly mean surface measurements of NH3, HNO3 and NO2 concentrations (passive samplers) together with simulated deposition velocities, and wet deposition fluxes from NH4+ and NO3- concentrations in single event rain samples (automated rain sampler). Annual rainfall amount was 2500 and 3160 mm for the two years. The average nitrogen deposition flux is estimated at 1.13 kgN.ha-1.yr-1 from dry processes and 5.52 kgN.ha-1.yr-1 from wet ones, i.e., an average annual total nitrogen flux of 6.6 kgN.ha-1.yr-1 deposited into the NT2 reservoir. The wet deposition contributes to 83% of the total N deposition. The nitrogen deposition budget has been also calculated over the rain tropical forest surrounding the reservoir. Due to higher dry deposition velocities above forested ecosystems, gaseous dry deposition flux is estimated at 4.0 kgN.ha-1.yr-1 leading to a total nitrogen deposition about 9.5 kgN.ha-1.yr-1. This result will be compared to nitrogen deposition in the African equatorial forested ecosystems in the framework of the IDAF program (IGAC-DEBITS-AFrica).

Depositional characteristics of atmospheric polybrominated diphenyl ethers on tree barks.

Science.gov (United States)

Chun, Man Young

2014-07-17

This study was conducted to determine the depositional characteristics of several tree barks, including Ginkgo (Ginkgo biloba), Pine (Pinus densiflora), Platanus (Platanus), and Metasequoia (Metasequoia glyptostroboides). These were used as passive air sampler (PAS) of atmospheric polybrominated diphenyl ethers (PBDEs). Tree barks were sampled from the same site. PBDEs were analyzed by highresolution gas chromatography/high-resolution mass spectrometer, and the lipid content was measured using the gravimetric method by n-hexane extraction. Gingko contained the highest lipid content (7.82 mg/g dry), whereas pine (4.85 mg/g dry), Platanus (3.61 mg/g dry), and Metasequoia (0.97 mg/g dry) had relatively lower content. The highest total PBDEs concentration was observed in Metasequoia (83,159.0 pg/g dry), followed by Ginkgo (53,538.4 pg/g dry), Pine (20,266.4 pg/g dry), and Platanus (12,572.0 pg/g dry). There were poor correlations between lipid content and total PBDE concentrations in tree barks (R(2)=0.1011, p =0.682). Among the PBDE congeners, BDE 206, 207 and 209 were highly brominated PBDEs that are sorbed to particulates in ambient air, which accounted for 90.5% (84.3-95.6%) of the concentration and were therefore identified as the main PBDE congener. The concentrations of particulate PBDEs deposited on tree barks were dependent on morphological characteristics such as surface area or roughness of barks. Therefore, when using the tree barks as the PAS of the atmospheric PBDEs, samples belonging to same tree species should be collected to reduce errors and to obtain reliable data.

Quantifying particulate matter deposition in Niwot Ridge, Colorado: Collection of dry deposition using marble inserts and particle imaging using the FlowCAM

Science.gov (United States)

Goss, Natasha R.; Mladenov, Natalie; Seibold, Christine M.; Chowanski, Kurt; Seitz, Leslie; Wellemeyer, T. Barret; Williams, Mark W.

2013-12-01

Atmospheric wet and dry deposition are important sources of carbon for remote alpine lakes and soils. The carbon inputs from dry deposition in alpine National Atmospheric Deposition Program (NADP) collectors, including aeolian dust and biological material, are not well constrained due to difficulties in retaining particulate matter in the collectors. Here, we developed and tested a marble insert for dry deposition collection at the Niwot Ridge Long Term Ecological Research Station (NWT LTER) Soddie site (3345 m) between 24 May and 8 November 2011. We conducted laboratory tests of the insert's effect on particulate matter (PM) mass and non-purgeable organic carbon (DOC) and found that the insert did not significantly change either measurement. Thus, the insert may enable dry deposition collection of PM and DOC at NADP sites. We then developed a method for enumerating the collected wet and dry deposition with the Flow Cytometer and Microscope (FlowCAM), a dynamic-image particle analysis tool. The FlowCAM has the potential to establish morphology, which affects particle settling and retention, through particle diameter and aspect ratio. Particle images were used to track the abundance of pollen grains over time. Qualitative image examination revealed that most particles were biological in nature, such as intact algal cells and pollen. Dry deposition loading to the Soddie site as determined by FlowCAM measurements was highly variable, ranging from 100 to >230 g ha-1 d-1 in June-August 2011 and peaking in late June. No significant difference in diameter or aspect ratio was found between wet and dry deposition, suggesting fundamental similarities between those deposition types. Although FlowCAM statistics and identification of particle types proved insightful, our total-particle enumeration method had a high variance and underestimated the total number of particles when compared to imaging of relatively large volumes (60-125 mL) from a single sample. We recommend use of

Atmospheric mercury deposition to forests in the eastern USA

International Nuclear Information System (INIS)

Risch, Martin R.; DeWild, John F.; Gay, David A.; Zhang, Leiming; Boyer, Elizabeth W.; Krabbenhoft, David P.

2017-01-01

Atmospheric mercury (Hg) deposition to forests is important because half of the land cover in the eastern USA is forest. Mercury was measured in autumn litterfall and weekly precipitation samples at a total of 27 National Atmospheric Deposition Program (NADP) monitoring sites in deciduous and mixed deciduous-coniferous forests in 16 states in the eastern USA during 2007–2014. These simultaneous, uniform, repeated, annual measurements of forest Hg include the broadest area and longest time frame to date. The autumn litterfall-Hg concentrations and litterfall mass at the study sites each year were combined with annual precipitation-Hg data. Rates of litterfall-Hg deposition were higher than or equal to precipitation-Hg deposition rates in 70% of the annual data, which indicates a substantial contribution from litterfall to total atmospheric-Hg deposition. Annual litterfall-Hg deposition in this study had a median of 11.7 μg per square meter per year (μg/m 2 /yr) and ranged from 2.2 to 23.4 μg/m 2 /yr. It closely matched modeled dry-Hg deposition, based on land cover at selected NADP Hg-monitoring sites. Mean annual atmospheric-Hg deposition at forest study sites exhibited a spatial pattern partly explained by statistical differences among five forest-cover types and related to the mapped density of Hg emissions. Forest canopies apparently recorded changes in atmospheric-Hg concentrations over time because litterfall-Hg concentrations decreased year to year and litterfall-Hg concentrations were significantly higher in 2007–2009 than in 2012–2014. These findings reinforce reported decreases in Hg emissions and atmospheric elemental-Hg concentrations during this same time period. Methylmercury (MeHg) was detected in all litterfall samples at all sites, compared with MeHg detections in less than half the precipitation samples at selected sites during the study. These results indicate MeHg in litterfall is a pathway into the terrestrial food web where it can

Total dissolved atmospheric nitrogen deposition in the anoxic Cariaco basin

Science.gov (United States)

Rasse, R.; Pérez, T.; Giuliante, A.; Donoso, L.

2018-04-01

Atmospheric deposition of total dissolved nitrogen (TDN) is an important source of nitrogen for ocean primary productivity that has increased since the industrial revolution. Thus, understanding its role in the ocean nitrogen cycle will help assess recent changes in ocean biogeochemistry. In the anoxic Cariaco basin, the place of the CARIACO Ocean Time-Series Program, the influence of atmospherically-deposited TDN on marine biogeochemistry is unknown. In this study, we measured atmospheric TDN concentrations as dissolved organic (DON) and inorganic (DIN) nitrogen (TDN = DIN + DON) in atmospheric suspended particles and wet deposition samples at the northeast of the basin during periods of the wet (August-September 2008) and dry (March-April 2009) seasons. We evaluated the potential anthropogenic N influences by measuring wind velocity and direction, size-fractionated suspended particles, chemical traces and by performing back trajectories. We found DIN and DON concentration values that ranged between 0.11 and 0.58 μg-N m-3 and 0.11-0.56 μg-N m-3 in total suspended particles samples and between 0.08 and 0.54 mg-N l-1 and 0.02-1.3 mg-N l-1 in wet deposition samples, respectively. Continental air masses increased DON and DIN concentrations in atmospheric suspended particles during the wet season. We estimate an annual TDN atmospheric deposition (wet + particles) of 3.6 × 103 ton-N year-1 and concluded that: 1) Atmospheric supply of TDN plays a key role in the C and N budget of the basin because replaces a fraction of the C (20% by induced primary production) and N (40%) removed by sediment burial, 2) present anthropogenic N could contribute to 30% of TDN atmospheric deposition in the basin, and 3) reduced DON (gas + particles) should be a significant component of bulk N deposition.

Atmospheric depositions around a heavily industrialized area in a seasonally dry tropical environment of India

International Nuclear Information System (INIS)

Singh, Raj Kumar; Agrawal, Madhoolika

2005-01-01

Clear and throughfall bulk depositions were collected in the downwind of a highly industrialized region in Sonbhadra district of India to estimate the influence of anthropogenic activities on chemical composition of depositions. Significant spatial and temporal variations in depositions of cations and anions were observed. Depositions were higher near the thermal power stations and coalmines as compared to distantly situated site. Seasonally summer samples showed maximum cation and anion depositions followed by winter and minimum in rainy season. The mean pH of the depositions indicates that rainfall in the area is alkaline. Among the anions, maximum deposition was recorded for SO 4 2- followed by NO 3 - and minimum for Cl - . Among the cations, Ca 2+ deposition was maximum followed by NH 4 + . Na + , K + and Mg 2+ deposition rates showed more or less similar values. The depositions of cations and anions as well as pH were higher in throughfall than clearfall samples. Results of the present study suggest that atmospheric depositions are strongly modified due to thermal power stations and coal mines in the area. - Atmospheric abundance of cations have neutralized the acidity of depositions around a heavily industrialized area in India

Direct and indirect atmospheric deposition of PCBs to the Delaware River watershed.

Science.gov (United States)

Totten, Lisa A; Panangadan, Maya; Eisenreich, Steven J; Cavallo, Gregory J; Fikslin, Thomas J

2006-04-01

Atmospheric deposition can be an important source of PCBs to aquatic ecosystems. To develop the total maximum daily load (TMDL) for polychlorinated biphenyls (PCBs) for the tidal Delaware River (water-quality Zones 2-5), estimates of the loading of PCBs to the river from atmospheric deposition were generated from seven air-monitoring sites along the river. This paper presents the atmospheric PCB data from these sites, estimates direct atmospheric deposition fluxes, and assesses the importance of atmospheric deposition relative to other sources of PCBs to the river. Also, the relationship between indirect atmospheric deposition and PCB loads from minor tributaries to the Delaware River is discussed. Data from these sites revealed high atmospheric PCB concentrations in the Philadelphia/Camden urban area and lower regional background concentrations in the more remote areas. Wet, dry particle, and gaseous absorption deposition are estimated to contribute about 0.6, 1.8, and 6.5 kg year-(-1) sigmaPCBs to the River, respectively, exceeding the TMDL of 0.139 kg year(-1) by more than an order of magnitude. Penta-PCB watershed fluxes were obtained by dividing the tributary loads by the watershed area. The lowest of these watershed fluxes are less than approximately 1 ng m(-2) day(-1) for penta-PCB and probably indicates pristine watersheds in which PCB loads are dominated by atmospheric deposition. In these watersheds, the pass-through efficiency of PCBs is estimated to be on the order of 1%.

Zn isotope study of atmospheric emissions and dry depositions within a 5 km radius of a Pb-Zn refinery

Science.gov (United States)

Mattielli, Nadine; Petit, Jérôme C. J.; Deboudt, Karine; Flament, Pascal; Perdrix, Esperanza; Taillez, Aurélien; Rimetz-Planchon, Juliette; Weis, Dominique

The present paper examines the use of zinc isotopes as tracers of atmospheric sources and focuses on the potential fractionation of Zn isotopes through anthropogenic processes. In order to do so, Zn isotopic ratios are measured in enriched ores and airborne particles associated with pyrometallurgical activities of one of the major Pb-Zn refineries in France. Supporting the isotopic investigation, this paper also compares morphological and chemical characteristics of Zn particles collected on dry deposition plates ("environmental samples") placed within a 5 km radius of the smelter, with those of Zn particles collected inside the plant ("process samples"), i.e. dust collected from the main exhaust system of the plant. To ensure a constant isotopic "supply", the refinery processed a specific set of ores during the sampling campaigns, as agreed with the executive staff of the plant. Enriched ores and dust produced by the successive Zn extraction steps show strong isotope fractionation (from -0.66 to +0.22‰) mainly related to evaporation processes within the blast furnaces. Dust from the main chimney displays a δ 66Zn value of -0.67‰. Application of the Rayleigh equation to evaluate the fractionation factor associated with the Zn vapor produced after a free evaporation gives a range of αore/vapor from 1.0004 to 1.0008. The dry deposits, collected on plates downwind of the refinery, display δ 66Zn variations of up to +0.7‰. However, it is to be noted that between 190 and 1250 m from the main chimney of the refinery, the dry deposits show a high level of large (>10 μm) Zn, S, Fe and O bearing aggregates characterized by positive δ 66Zn values (+0.02 to +0.19‰). These airborne particles probably derive from the re-suspension of slag heaps and local emissions from the working-units. In contrast, from 1720 to 4560 m, the dry deposits are comprised of small (PM10) particles, including spherical Zn-bearing aggregates, showing negative δ 66Zn values (-0.52 to -0

Depositional characteristics of atmospheric polybrominated diphenyl ethers on tree barks

Directory of Open Access Journals (Sweden)

Man Young Chun

2014-07-01

Full Text Available Objectives This study was conducted to determine the depositional characteristics of several tree barks, including Ginkgo (Ginkgo biloba, Pine (Pinus densiflora, Platanus (Platanus, and Metasequoia (Metasequoia glyptostroboides. These were used as passive air sampler (PAS of atmospheric polybrominated diphenyl ethers (PBDEs. Methods Tree barks were sampled from the same site. PBDEs were analyzed by highresolution gas chromatography/high-resolution mass spectrometer, and the lipid content was measured using the gravimetric method by n-hexane extraction. Results Gingko contained the highest lipid content (7.82 mg/g dry, whereas pine (4.85 mg/g dry, Platanus (3.61 mg/g dry, and Metasequoia (0.97 mg/g dry had relatively lower content. The highest total PBDEs concentration was observed in Metasequoia (83,159.0 pg/g dry, followed by Ginkgo (53,538.4 pg/g dry, Pine (20,266.4 pg/g dry, and Platanus (12,572.0 pg/g dry. There were poor correlations between lipid content and total PBDE concentrations in tree barks (R2=0.1011, p =0.682. Among the PBDE congeners, BDE 206, 207 and 209 were highly brominated PBDEs that are sorbed to particulates in ambient air, which accounted for 90.5% (84.3-95.6% of the concentration and were therefore identified as the main PBDE congener. The concentrations of particulate PBDEs deposited on tree barks were dependent on morphological characteristics such as surface area or roughness of barks. Conclusions Therefore, when using the tree barks as the PAS of the atmospheric PBDEs, samples belonging to same tree species should be collected to reduce errors and to obtain reliable data.

Diurnal and seasonal variability in size-dependent atmospheric deposition fluxes of polycyclic aromatic hydrocarbons in an urban center

Science.gov (United States)

Zhang, Kai; Zhang, Bao-Zhong; Li, Shao-Meng; Zhang, Lei-Ming; Staebler, Ralf; Zeng, Eddy Y.

2012-09-01

Atmospheric gaseous and size-segregated particle samples were collected from urban Guangzhou at the heights of 100 and 150 m above the ground in daytime and at night in August and December 2010, and were analyzed for polycyclic aromatic hydrocarbons (PAHs). Particulate PAHs were more abundant at night than in daytime, and significantly higher in winter than in summer. The observed vertical, diurnal, and seasonal variability in the occurrences of PAH were attributed to varying meteorological conditions and atmospheric boundary layers. More than 60% of the particulate PAHs were contained in particles in the accumulation mode with an aerodynamic diameter (Dp) in the range of 0.1-1.8 μm. Different mass transfer velocities by volatilization and condensation are considered the main causes for the different particle size distributions among individual PAHs, while combustion at different temperatures and atmospheric transport were probable causes of the observed seasonal variation in the size distribution of PAHs. Based on the modeled size-dependent dry deposition velocities, daily mean dry deposition fluxes of particulate PAHs ranged from 604 to 1190 ng m-2 d-1, with PAHs in coarse particles (Dp > 1.8 μm) accounting for 55-95% of the total fluxes. In addition, gaseous PAHs were estimated to contribute 0.6-3.1% to the total dry deposition fluxes if a conservative dry deposition velocity for gaseous species (2 × 10-4 m s-1) were used. Finally, disequilibrium phase partitioning, meteorological conditions and atmospheric transport were regarded as the main reasons for the variances in dry deposition velocities of individual PAHs.

Dry deposition to vegetated surfaces: parametric dependencies

International Nuclear Information System (INIS)

Underwood, B.Y.

1987-12-01

The dry deposition velocity of airborne pollutants to vegetated surfaces depends on the physico-chemical form of the pollutant, on meteorological conditions (windspeed, atmospheric stability) and on characteristics of the surface cover. This report examines these dependencies, drawing on experimental data and on information from theoretical analyses. A canopy model is outlined which uses first-order closure of the equations for turbulent transport of momentum (or matter), with losses of momentum (or matter) to individual canopy elements parameterised in terms of the mean windspeed: the model has previously been tested against experimental data on an artificial 'grass' canopy. The model is used to elucidate the features of the dependence of deposition velocity on windspeed and on whether the pollutant is in gaseous or particulate form: in the former case, the dependence on the molecular diffusivity of the gas is shown; in the latter case, dependencies on particle diameter and density are deduced. The predictions are related to available measurements. Additional hypotheses are introduced to treat the influence of atmospheric stability on deposition, and the analysis is used to shed light on the somewhat confusing picture that has emerged from past experimental studies. In considering the dependence of deposition velocity on the structural properties of the vegetation, it is established that more parameters than the single one conventionally used -aerodynamic roughness length - are needed to characterise the surface cover. Some indications of the extent of variation in deposition velocity from one type of vegetation to another are elicited from the model. (author)

Quantification of Gaseous Elemental Mercury Dry Deposition to Environmental Surfaces using Mercury Stable Isotopes in a Controlled Environment

Science.gov (United States)

Rutter, A. P.; Schauer, J. J.; Shafer, M. M.; Olson, M.; Robinson, M.; Vanderveer, P.; Creswell, J. E.; Parman, A.; Mallek, J.; Gorski, P.

2009-12-01

Andrew P. Rutter (1) * *, James J, Schauer (1,2) *, Martin M. Shafer(1,2), Michael R. Olson (1), Michael Robinson (1), Peter Vanderveer (3), Joel Creswell (1), Justin L. Mallek (1), Andrew M. Parman (1) (1) Environmental Chemistry and Technology Program, 660 N. Park St, Madison, WI 53705. (2) Wisconsin State Laboratory of Hygiene, 2601 Agriculture Drive, Madison, WI 53718. (3) Biotron, University of Wisconsin - Madison, 2115 Observatory Drive, Madison, WI 53706 * Correspond author(jjschauer@wisc.edu) * *Presenting author (aprutter@wisc.edu) Abstract Gaseous elemental mercury (GEM) is the predominant component of atmospheric mercury outside of arctic depletion events, and locations where anthropogenic point sources are not influencing atmospheric concentrations. GEM constitutes greater than 99% of the mercury mass in most rural and remote locations. While dry and wet deposition of atmospheric mercury is thought to be dominated by oxidized mercury (a.k.a. reactive mercury), only small GEM uptake to environmental surfaces could impact the input of mercury to terrestrial and aquatic ecosystems. Dry deposition and subsequent re-emission of gaseous elemental mercury is a pathway from the atmosphere that remains only partially understood from a mechanistic perspective. In order to properly model GEM dry deposition and re-emission an understanding of its dependence on irradiance, temperature, and relative humidity must be measured and parameterized for a broad spectrum of environmental surfaces colocated with surrogate deposition surfaces used to make field based dry deposition measurements. Measurements of isotopically enriched GEM dry deposition were made with a variety of environmental surfaces in a controlled environment room at the University of Wisconsin Biotron. The experimental set up allowed dry deposition components which are not easily separated in the field to be decoupled. We were able to isolate surface transfer processes from variabilities caused by

Atmospheric deposition of heavy metals due to dry, wet and occult deposition at the altitude profile Achenkirch

International Nuclear Information System (INIS)

Stopper, S.

2001-12-01

The goal of this work was to determine the height dependence of the three types of deposition throughout a one year time period to be able to get information about their elevational and seasonal behavior. In the time period from October 1998 to November 1999 measurements of Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb, V and Zn in aerosol, rain and cloud water were conducted in the Achenkirch-Valley in Tyrol, Austria. Afterwards the dry and occult deposition were modeled. The estimated annual inputs of metals at the two measurement sites Christlumkopf (1758 m a.s.l.) Mueeggerkoel (940 m a.s.l.) and the limits of the national law for protection of forest are shown. The measured depositions at both sites were far below the legal regulations. Due to the much higher occult deposition ratio at the top of the mountain the total annual input at the Christlumkopf was higher than at the Mueeggerkoel. This indicates the potential importance of occult deposition. (author)

Atmospheric mercury deposition to forests in the eastern USA.

Science.gov (United States)

Risch, Martin R; DeWild, John F; Gay, David A; Zhang, Leiming; Boyer, Elizabeth W; Krabbenhoft, David P

2017-09-01

Atmospheric mercury (Hg) deposition to forests is important because half of the land cover in the eastern USA is forest. Mercury was measured in autumn litterfall and weekly precipitation samples at a total of 27 National Atmospheric Deposition Program (NADP) monitoring sites in deciduous and mixed deciduous-coniferous forests in 16 states in the eastern USA during 2007-2014. These simultaneous, uniform, repeated, annual measurements of forest Hg include the broadest area and longest time frame to date. The autumn litterfall-Hg concentrations and litterfall mass at the study sites each year were combined with annual precipitation-Hg data. Rates of litterfall-Hg deposition were higher than or equal to precipitation-Hg deposition rates in 70% of the annual data, which indicates a substantial contribution from litterfall to total atmospheric-Hg deposition. Annual litterfall-Hg deposition in this study had a median of 11.7 μg per square meter per year (μg/m 2 /yr) and ranged from 2.2 to 23.4 μg/m 2 /yr. It closely matched modeled dry-Hg deposition, based on land cover at selected NADP Hg-monitoring sites. Mean annual atmospheric-Hg deposition at forest study sites exhibited a spatial pattern partly explained by statistical differences among five forest-cover types and related to the mapped density of Hg emissions. Forest canopies apparently recorded changes in atmospheric-Hg concentrations over time because litterfall-Hg concentrations decreased year to year and litterfall-Hg concentrations were significantly higher in 2007-2009 than in 2012-2014. These findings reinforce reported decreases in Hg emissions and atmospheric elemental-Hg concentrations during this same time period. Methylmercury (MeHg) was detected in all litterfall samples at all sites, compared with MeHg detections in less than half the precipitation samples at selected sites during the study. These results indicate MeHg in litterfall is a pathway into the terrestrial food web where it can

Atmospheric dry and wet deposition of sulphur and nitrogen species and assessment of critical loads of acidic deposition exceedance in South Africa

Directory of Open Access Journals (Sweden)

Stuart J. Piketh

2011-03-01

Full Text Available We tested the hypothesis that acidic atmospheric pollution deposition, originating from the South African central industrial area, poses an environmental threat across a larger region within the dispersal footprint. A network of 37 passive monitoring sites to measure SO₂ and NO₂ was operated from August 2005 to September 2007. The area extended over the entire northern and eastern interior of South Africa. Monitoring locations were chosen to avoid direct impacts from local sources such as towns, mines and highways. Dry deposition rates of SO₂ and NO₂ were calculated from the measured concentrations. Concentrations of sulphur and nitrogen species in wet deposition from a previous study were used in conjunction with measured rainfall for the years 2006 and 2007 to estimate the wet deposition over the region. The calculated total (non-organic acidic deposition formed the basis for an assessment of exceedance of critical loads based on sensitivity of the regional soils. Regional soil sensitivity was determined by combining two major soil attributes available in the World Inventory of Soil Emission Potentials (International Soil Reference and Information Centre. Results indicate that certain parts of the central pollution source area on the South African Highveld have the potential for critical load exceedance, while limited areas downwind show lower levels of exceedance. Areas upwind and remote areas up and downwind, including forested areas of the Drakensberg escarpment, do not show any exceedance of the critical loads.

Source apportionment of atmospheric bulk deposition in the Belgrade urban area using Positive Matrix factorization

Science.gov (United States)

Tasić, M.; Mijić, Z.; Rajšić, S.; Stojić, A.; Radenković, M.; Joksić, J.

2009-04-01

The primary objective of the present study was to assess anthropogenic impacts of heavy metals to the environment by determination of total atmospheric deposition of heavy metals. Atmospheric depositions (wet + dry) were collected monthly, from June 2002 to December 2006, at three urban locations in Belgrade, using bulk deposition samplers. Concentrations of Fe, Al, Pb, Zn, Cu, Ni, Mn, Cr, V, As and Cd were analyzed using atomic absorption spectrometry. Based upon these results, the study attempted to examine elemental associations in atmospheric deposition and to elucidate the potential sources of heavy metal contaminants in the region by the use of multivariate receptor model Positive Matrix Factorization (PMF).

Source apportionment of atmospheric bulk deposition in the Belgrade urban area using Positive Matrix factorization

International Nuclear Information System (INIS)

Tasic, M; Mijic, Z; Rajsic, S; Stojic, A; Radenkovic, M; Joksic, J

2009-01-01

The primary objective of the present study was to assess anthropogenic impacts of heavy metals to the environment by determination of total atmospheric deposition of heavy metals. Atmospheric depositions (wet + dry) were collected monthly, from June 2002 to December 2006, at three urban locations in Belgrade, using bulk deposition samplers. Concentrations of Fe, Al, Pb, Zn, Cu, Ni, Mn, Cr, V, As and Cd were analyzed using atomic absorption spectrometry. Based upon these results, the study attempted to examine elemental associations in atmospheric deposition and to elucidate the potential sources of heavy metal contaminants in the region by the use of multivariate receptor model Positive Matrix Factorization (PMF).

Speciated particle dry deposition to the sea surface: Results from ASEPS '97

DEFF Research Database (Denmark)

Pryor, S.C.; Barthelmie, R.J.; Geernaert, L.L.S.

1999-01-01

on Precipitation Scavenging and Atmosphere-Surface Exchange Processes. AMS, Richland, Washington, USA, 12pp.) model to calculate size-segregated dry deposition of particle inorganic nitrogen compounds to the western Baltic during the late Spring of 1997 based on data collected as part of the Air-Sea Exchange...

Comparison of mercury mass loading in streams to atmospheric deposition in watersheds of Western North America: Evidence for non-atmospheric mercury sources

Science.gov (United States)

Domagalski, Joseph L.; Majewski, Michael S.; Alpers, Charles N.; Eckley, Chris S.; Eagles-Smith, Collin A.; Schenk, Liam N.; Wherry, Susan

2016-01-01

Annual stream loads of mercury (Hg) and inputs of wet and dry atmospheric Hg deposition to the landscape were investigated in watersheds of the Western United States and the Canadian-Alaskan Arctic. Mercury concentration and discharge data from flow gauging stations were used to compute annual mass loads with regression models. Measured wet and modeled dry deposition were compared to annual stream loads to compute ratios of Hg stream load to total Hg atmospheric deposition. Watershed land uses or cover included mining, undeveloped, urbanized, and mixed. Of 27 watersheds that were investigated, 15 had some degree of mining, either of Hg or precious metals (gold or silver), where Hg was used in the amalgamation process. Stream loads in excess of annual Hg atmospheric deposition (ratio > 1) were observed in watersheds containing Hg mines and in relatively small and medium-sized watersheds with gold or silver mines, however, larger watersheds containing gold or silver mines, some of which also contain large dams that trap sediment, were sometimes associated with lower load ratios (watersheds with natural vegetation tended to have low ratios of stream load to Hg deposition (watersheds (Mackenzie and Yukon Rivers) had a relatively elevated ratio of stream load to atmospheric deposition (0.27 and 0.74), possibly because of melting glaciers or permafrost releasing previously stored Hg to the streams. Overall, our research highlights the important role of watershed characteristics in determining whether a landscape is a net source of Hg or a net sink of atmospheric Hg.

Particle dry deposition to water surfaces: Processes and consequences

DEFF Research Database (Denmark)

Pryor, S.C.; Barthelmie, R.J.

2000-01-01

flux to coastal waters, atmosphere-surface exchange represents a significant component of the total flux and may be particularly critical during the summertime when both the riverine input and ambient nutrient concentrations are often at a minimum. In this chapter, we present an overview...... of the physical and chemical processes which dictate the quantity (and direction) of atmosphere-surface fluxes of trace chemicals to (and above) water surfaces with particular emphasis on the role of particles. Dry deposition (transfer to the surface in the absence of precipitation) of particles is determined...... efforts to simulate and measure fluxes close to the coastline. These arise in part from the complexity of atmospheric flow in this region where energy and chemical fluxes are highly inhomogeneous in space and time and thermally generated atmospheric circulations are commonplace. (C) 2000 Elsevier Science...

HTO deposition by vapor exchange between atmosphere and soil

International Nuclear Information System (INIS)

Bunnenberg, C.

1989-01-01

HTO deposition to soils occurs by vapor exchange between atmosphere and soil-air, when the concentration gradient is directed downwards, and it is principally independent from simultaneous transport of H 2 O. In relatively dry top soil, which is frequently the case, as it tries to attain equilibrium with the air humidity, HTO diffuses into deeper soil driven by the same mechanisms that caused the deposition process. The resulting HTO profile is depending on the atmospheric supply and the soil physical conditions, and it is the source for further tritium pathways, namely root uptake by plants and reemission from soil back into the ground-level air. Simulation experiments with soil columns exposed to HTO labeled atmospheres have proved the theoretical expectation that under certain boundary conditions the HTO profile can be described by an error function. The key parameter is the effective diffusion coefficient, which in turn is a function of the sorption characteristics of the particular soil. (orig.) [de

Evaluating the Contributions of Atmospheric Deposition of Carbon and Other Nutrients to Nitrification in Alpine Environments

Science.gov (United States)

Oldani, K. M.; Mladenov, N.; Williams, M. W.

2013-12-01

The Colorado Front Range of the Rocky Mountains contains undeveloped, barren soils, yet in this environment there is strong evidence for a microbial role in increased nitrogen (N) export. Barren soils in alpine environments are severely carbon-limited, which is the main energy source for microbial activity and sustenance of life. It has been shown that atmospheric deposition can contain high amounts of organic carbon (C). Atmospheric pollutants, dust events, and biological aerosols, such as bacteria, may be important contributors to the atmospheric organic C load. In this stage of the research we evaluated seasonal trends in the chemical composition and optical spectroscopic (fluorescence and UV-vis absorbance) signatures of snow, wet deposition, and dry deposition in an alpine environment at Niwot Ridge in the Rocky Mountains of Colorado to obtain a better understanding of the sources and chemical character of atmospheric deposition. Our results reveal a positive trend between dissolved organic carbon concentrations and calcium, nitrate and sulfate concentrations in wet and dry deposition, which may be derived from such sources as dust and urban air pollution. We also observed the presence of seasonally-variable fluorescent components that may be attributed to fluorescent pigments in bacteria. These results are relevant because atmospheric inputs of carbon and other nutrients may influence nitrification in barren, alpine soils and, ultimately, the export of nitrate to alpine watersheds.

Year-round atmospheric wet and dry deposition of nitrogen and phosphorus on water and land surfaces in Nanjing, China.

Science.gov (United States)

Sun, Liying; Li, Bo; Ma, Yuchun; Wang, Jinyang; Xiong, Zhengqin

2013-06-01

The dry deposition of ammonium, nitrate, and total phosphorus (TP) to both water (DW) and land (DD) surfaces, along with wet deposition, were simultaneously monitored from March 2009 to February 2011 in Nanjing, China. Results showed that wet deposition of total phosphorus was 1.1 kg phosphorus ha (-1)yr(-1), and inorganic nitrogen was 28.7 kg nitrogen ha (-1)yr(-1), with 43% being ammonium nitrogen. Dry deposition of ammonium, nitrate, and total phosphorus, measured by the DW/DD method, was 7.5/2.2 kg nitrogen ha (-1)yr(-1), 6.3/ 4.9 kg nitrogen ha (-1)yr(-1), and 1.9/0.4 kg phosphorus ha (-1)yr(-1), respectively. Significant differences between the DW and DD methods indicated that both methods should be employed simultaneously when analyzing deposition to aquatic and terrestrial ecosystems in watershed areas. The dry deposition of ammonium, nitrate, and total phosphorus contributed 38%, 28%, and 63%, respectively, to the total deposition in the simulated aquatic ecosystem; this has significance for the field of water eutrophication control.

Comparison of snowpack and winter wet-deposition chemistry in the Rocky Mountains, USA: implications for winter dry deposition

Science.gov (United States)

Clow, David W.; Ingersoll, George P.; Mast, M. Alisa; Turk, John T.; Campbell, Donald H.

Depth-integrated snowpack chemistry was measured just prior to maximum snowpack depth during the winters of 1992-1999 at 12 sites co-located with National Atmospheric Deposition Program/National Trend Network (NADP/NTN) sites in the central and southern Rocky Mountains, USA. Winter volume-weighted mean wet-deposition concentrations were calculated for the NADP/NTN sites, and the data were compared to snowpack concentrations using the paired t-test and the Wilcoxon signed-rank test. No statistically significant differences were indicated in concentrations of SO 42- or NO 3- ( p>0.1). Small, but statistically significant differences ( p⩽0.03) were indicated for all other solutes analyzed. Differences were largest for Ca 2+ concentrations, which on average were 2.3 μeq l -1 (43%) higher in the snowpack than in winter NADP/NTN samples. Eolian carbonate dust appeared to influence snowpack chemistry through both wet and dry deposition, and the effect increased from north to south. Dry deposition of eolian carbonates was estimated to have neutralized an average of 6.9 μeq l -1 and a maximum of 12 μeq l -1 of snowpack acidity at the southernmost sites. The good agreement between snowpack and winter NADP/NTN SO 42- and NO 3- concentrations indicates that for those solutes the two data sets can be combined to increase data density in high-elevation areas, where few NADP/NTN sites exist. This combination of data sets will allow for better estimates of atmospheric deposition of SO 42- and NO 3- across the Rocky Mountain region.

Seasonal atmospheric deposition variations of polychlorinated biphenyls (PCBs) and comparison of some deposition sampling techniques.

Science.gov (United States)

Birgül, Askın; Tasdemir, Yücel

2011-03-01

Ambient air and bulk deposition samples were collected between June 2008 and June 2009. Eighty-three polychlorinated biphenyl (PCB) congeners were targeted in the samples. The average gas and particle PCB concentrations were found as 393 ± 278 and 70 ± 102 pg/m(3), respectively, and 85% of the atmospheric PCBs were in the gas phase. Bulk deposition samples were collected by using a sampler made of stainless steel. The average PCB bulk deposition flux value was determined as 6,020 ± 4,350 pg/m(2) day. The seasonal bulk deposition fluxes were not statistically different from each other, but the summer flux had higher values. Flux values differed depending on the precipitation levels. The average flux value in the rainy periods was 7,480 ± 4,080 pg/m(2) day while the average flux value in dry periods was 5,550 ± 4,420 pg/m(2) day. The obtained deposition values were lower than the reported values given for the urban and industrialized areas, yet close to the ones for the rural sites. The reported deposition values were also influenced by the type of the instruments used. The average dry deposition and total deposition velocity values calculated based on deposition and concentration values were found as 0.23 ± 0.21 and 0.13 ± 0.13 cm/s, respectively.

Comparison of mercury mass loading in streams to atmospheric deposition in watersheds of Western North America: Evidence for non-atmospheric mercury sources

Science.gov (United States)

Domagalski, Joseph L.; Majewski, Michael S.; Alpers, Charles N.; Eckley, Chris S.; Eagles-Smith, Collin A.; Schenk, Liam N.; Wherry, Susan

2016-01-01

Annual stream loads of mercury (Hg) and inputs of wet and dry atmospheric Hg deposition to the landscape were investigated in watersheds of the Western United States and the Canadian-Alaskan Arctic. Mercury concentration and discharge data from flow gauging stations were used to compute annual mass loads with regression models. Measured wet and modeled dry deposition were compared to annual stream loads to compute ratios of Hg stream load to total Hg atmospheric deposition. Watershed land uses or cover included mining, undeveloped, urbanized, and mixed. Of 27 watersheds that were investigated, 15 had some degree of mining, either of Hg or precious metals (gold or silver), where Hg was used in the amalgamation process. Stream loads in excess of annual Hg atmospheric deposition (ratio > 1) were observed in watersheds containing Hg mines and in relatively small and medium-sized watersheds with gold or silver mines, however, larger watersheds containing gold or silver mines, some of which also contain large dams that trap sediment, were sometimes associated with lower load ratios (< 0.2). In the non-Arctic regions, watersheds with natural vegetation tended to have low ratios of stream load to Hg deposition (< 0.1), whereas urbanized areas had higher ratios (0.34–1.0) because of impervious surfaces. This indicated that, in ecosystems with natural vegetation, Hg is retained in the soil and may be transported subsequently to streams as a result of erosion or in association with dissolved organic carbon. Arctic watersheds (Mackenzie and Yukon Rivers) had a relatively elevated ratio of stream load to atmospheric deposition (0.27 and 0.74), possibly because of melting glaciers or permafrost releasing previously stored Hg to the streams. Overall, our research highlights the important role of watershed characteristics in determining whether a landscape is a net source of Hg or a net sink of atmospheric Hg.

Short-term variability of 7Be atmospheric deposition and watershed response in a Pacific coastal stream, Monterey Bay, California, USA

International Nuclear Information System (INIS)

Conaway, Christopher H.; Storlazzi, Curt D.; Draut, Amy E.; Swarzenski, Peter W.

2013-01-01

Beryllium-7 is a powerful and commonly used tracer for environmental processes such as watershed sediment provenance, soil erosion, fluvial and nearshore sediment cycling, and atmospheric fallout. However, few studies have quantified temporal or spatial variability of 7 Be accumulation from atmospheric fallout, and parameters that would better define the uses and limitations of this geochemical tracer. We investigated the abundance and variability of 7 Be in atmospheric deposition in both rain events and dry periods, and in stream surface-water samples collected over a ten-month interval at sites near northern Monterey Bay (37°N, 122°W) on the central California coast, a region characterized by a rainy winters, dry summers, and small mountainous streams with flashy hydrology. The range of 7 Be activity in rainwater samples from the main sampling site was 1.3–4.4 Bq L −1 , with a mean (±standard deviation) of 2.2 ± 0.9 Bq L −1 , and a volume-weighted average of 2.0 Bq L −1 . The range of wet atmospheric deposition was 18–188 Bq m −2 per rain event, with a mean of 72 ± 53 Bq m −2 . Dry deposition fluxes of 7 Be ranged from less than 0.01 up to 0.45 Bq m −2 d −1 , with an estimated dry season deposition of 7 Bq m −2 month −1 . Annualized 7 Be atmospheric deposition was approximately 1900 Bq m −2 yr −1 , with most deposition via rainwater (>95%) and little via dry deposition. Overall, these activities and deposition fluxes are similar to values found in other coastal locations with comparable latitude and Mediterranean-type climate. Particulate 7 Be values in the surface water of the San Lorenzo River in Santa Cruz, California, ranged from −1 to 0.6 Bq g −1 , with a median activity of 0.26 Bq g −1 . A large storm event in January 2010 characterized by prolonged flooding resulted in the entrainment of 7 Be-depleted sediment, presumably from substantial erosion in the watershed. There were too few particulate 7 Be data over the storm

Elevated atmospheric deposition and dynamics of mercury in a remote upland forest of southwestern China

International Nuclear Information System (INIS)

Fu Xuewu; Feng Xinbin; Zhu Wanze; Rothenberg, S.; Yao Heng; Zhang Hui

2010-01-01

Mt. Gongga area in southwest China was impacted by Hg emissions from industrial activities and coal combustion, and annual means of atmospheric TGM and PHg concentrations at a regional background station were 3.98 ng m -3 and 30.7 pg m -3 , respectively. This work presents a mass balance study of Hg in an upland forest in this area. Atmospheric deposition was highly elevated in the study area, with the annual mean THg deposition flux of 92.5 μg m -2 yr -1 . Total deposition was dominated by dry deposition (71.8%), and wet deposition accounted for the remaining 28.2%. Forest was a large pool of atmospheric Hg, and nearly 76% of the atmospheric input was stored in forest soil. Volatilization and stream outflow were identified as the two major pathways for THg losses from the forest, which yielded mean output fluxes of 14.0 and 8.6 μg m -2 yr -1 , respectively. - Upland forest ecosystem is a great sink of atmospheric mercury in southwest China.

Dry deposition velocities in the global multi-scale CTM MOCAGE

Science.gov (United States)

Michou, M.; Peuch, V.-H.

2003-04-01

Surface exchanges considered in the MOCAGE multiscale Chemistry and Transport Model (CTM) of Météo-France include dry deposition of gaseous species. To compute realistic time-dependent fluxes at the surface, a 2D interface between MOCAGE and ARPEGE, the French operational numerical weather prediction model, has been developed. Dry deposition of species including ozone, sulfur dioxide, nitrogen-containing compounds, long-lived and short-lived intermediates organic compounds, have been parameterised according to the [Wesely, 1989] scheme. A number of modifications has been made, for instance concerning the deposition against wet surfaces. The formulation of the aerodynamic resistance follows [Louis, 1979], and that of the stomatal resistance, the Interaction Soil Biosphere Atmosphere (ISBA) Météo-France scheme. Resistances are computed using the surface meteorological fields obtained from the analyses or forecasts of ARPEGE. Vegetation fields such as the Leaf Area Index are prescribed with a one-degree spatial resolution at the global scale, and a five-minute resolution over Europe. Calculated dry deposition velocities of ozone, sulfur dioxide and nitric acid have been evaluated against field experimental data at various locations around the world, from tropical regions, rain forest or savannah over Central Africa and Amazonia (EXPRESSO and LBA campaigns), to Mediterranean regions, including forested and crop sites (ESCOMPTE campaign), and temperate areas (deciduous and evergreen forests). Hourly values, monthly and seasonal means have been examined, as well as the impact of the model resolution, from 2 degrees over the globe to 0.08 degrees over regional domains. The contributions to the global budget of ozone of the deposition fluxes in these different regions of the globe will be also presented.

Seasonal and annual variations and regional characteristics of wet and dry deposition amounts in East Asian region

Science.gov (United States)

Sato, K.; Tsuyoshi, O.; Endo, T.; Yagoh, H.; Matsuda, K.

2011-12-01

Emission of sulfur and nitrogen compounds in Asian region has been remarkably increased with recent rapid economical growth (Ohara et al., 2007). To appropriately assess the influence of air pollutants on the ecosystem, it is important to quantitatively determine the atmospheric deposition of air pollutants. Here, Seasonal and annual variations and regional characteristics of estimated wet and dry deposition amounts at 27 monitoring sites of Acid Deposition Monitoring Network in East Asia (EANET) from 2003 to 2009 are discussed. Wet deposition sample was collected every 24 hours or 1 week by a wet only sampler. Wet deposition amounts were calculated by the product of the volume-weighted concentrations of ionic species (SO42-, NO3-, and NH4+) in the precipitation and precipitation amount measured by a standard rain gauge at each site. Dry deposition amount was estimated by the inferential method which was originated the model developed by Wesely and Hicks (1977) and modified by Matsuda (2008). The components examined for dry deposition were sulfur compounds (gaseous SO2 and particulate SO42-) and nitrogen compounds (gaseous HNO3 and NH3, particulate NO3- and NH4+). Dry deposition was calculated by the product of the deposition velocity estimated by the inferential method for forest and grass surfaces and the monitored air concentration of each compound. The mean annual dry deposition amounts for sulfur and nitrogen compounds in Japanese sites were in the range of 5-37 and 7-50 mmol m-2 year-1, respectively. The regional characteristics of dry deposition amounts in Japan were similar between sulfur and nitrogen compounds, which showed higher deposition in the Sea of Japan side and the western Japan. The mean annual total (wet + dry) deposition amounts for sulfur and nitrogen compounds in Japanese sites were in the range of 28-77 and 22-130 mmol m-2 year-1, respectively. The contributions of dry deposition to the total deposition amounts were 10-55% and 13-56% for

Forest canopy uptake of atmospheric nitrogen deposition at eastern U.S. conifer sites: Carbon storage implications?

Science.gov (United States)

Herman Sievering; Ivan Fernandez; John Lee; John Hom; Lindsey Rustad

2000-01-01

Dry deposition determinations, along with wet deposition and throughfall (TF) measurements, at a spruce fir forest in central Maine were used to estimate the effect of atmospherically deposited nitrogen (N) uptake on forest carbon storage. Using nitric acid and particulate N as well as TF ammonium and nitrate data, the growing season (May-October) net canopy uptake of...

Trace elements in rainwater and dry deposition around a smelting complex

Energy Technology Data Exchange (ETDEWEB)

Beavington, F

1977-06-01

A number of plastic raingauges were set up at various distances around a smelting complex (copper smelter and steelworks) in Wollongong, Australia, to determine the pattern of total atmospheric deposition (rainwater and dry deposition) of copper, zinc, lead, cadmium, iron and manganese. At the site nearest the smelter, total deposition of these metals (6N HCl soluble) in kg/ha over a period of twelve months was 30.7 copper, 8.4 zinc, 4.7 lead, 0.19 cadmium, 42.6 iron and 1.5 manganese. These levels were considerably higher than at a distant rural site where background levels were similar to those reported for the United Kingdom. The pattern of deposition of metals over Wollongong accords with levels of metals previously reported in surface soil, herbage and leaf vegetables.

Transfer of gaseous iodine (I2) from atmosphere to rice grains through dry deposition

International Nuclear Information System (INIS)

Uchida, Shigeo; Muramatsu, Yasuyuki; Sumiya, Misako; Ohmomo, Yoichiro

1989-01-01

The report briefly outlines parameters required to determine the transfer of 129 I from the atmosphere to rice grains, and presents results of a study in which the transfer of iodine from the atmosphere to rice grains is calculated using empirically determined parameters. There are four major parameters required for the calculation: (1) the major transfer route (translocation either from leaves or from the surface of hulls to rice grains), (2) rate of deposition onto the surface of leaves or hulls, (3) biological half-life of iodine deposited on leaves or hulls, and (4) either the rate of translocation from leaves to hulls (where the translocation from leaves is the major route) or the ratio of iodine distribution among hulls, unpolished rice grains, and polished rice grains (where the translocation from hulls is the major route). Techniques available to determine the translocation route, deposition rate, biological half-life and distribution ratio are outlined. Chemical forms of iodine, parameters relating to the transfer of gaseous iodine to paddy rice, and calculation models are also described. (N,K.)

Dry deposition fluxes and deposition velocities of trace metals in the Tokyo metropolitan area measured with a water surface sampler.

Science.gov (United States)

Sakata, Masahiro; Marumoto, Kohji

2004-04-01

Dry deposition fluxes and deposition velocities (=deposition flux/atmospheric concentration) for trace metals including Hg, Cd, Cu, Mn, Pb, and Zn in the Tokyo metropolitan area were measured using an improved water surface sampler. Mercury is deposited on the water surface in both gaseous (reactive gaseous mercury, RGM) and particulate (particulate mercury, Hg(p)) forms. The results based on 1 yr observations found that dry deposition plays a significant if not dominant role in trace metal deposition in this urban area, contributing fluxes ranging from 0.46 (Cd) to 3.0 (Zn) times those of concurrent wet deposition fluxes. The deposition velocities were found to be dependent on the deposition of coarse particles larger than approximately 5 microm in diameter on the basis of model calculations. Our analysis suggests that the 84.13% diameter is a more appropriate index for each deposited metal than the 50% diameter in the assumed undersize log-normal distribution, because larger particles are responsible for the flux. The deposition velocities for trace metals other than mercury increased exponentially with an increase in their 84.13% diameters. Using this regression equation, the deposition velocities for Hg(p) were estimated from its 84.13% diameter. The deposition fluxes for Hg(p) calculated from the estimated velocities tended to be close to the mercury fluxes measured with the water surface sampler during the study periods except during summer.

Identification sources of pollen spectra in dry and wet atmospheric deposition in the forest-steppe zone of Altai Krai (Russia)

Science.gov (United States)

Ryabchinskaya, Natalia; Nenasheva, Galina; Malygina, Natalia

2015-04-01

Pollen spectra circulating in the atmosphere contain the important information about primary biological aerosol particles (PBAP), worldwide interest in which has significantly increased in recent decades [Despres, 2012]. It is related to the fact that many researchers suggest primary aerosols as a condensation nucleus significantly affected on the formation of clouds and precipitation and, consequently, on the hydrological cycle and climate, especially at the regional level [Andreae et al., 2008; Poschlet et al., 2010; Prenni et al., 2009]. We present the comparison of pollen spectra obtained during the dry and wet atmospheric deposition in Altai Krai (Russia) and identification of the sources/regions of their receipts. Altai Krai is located in the center of the Eurasian continent, at the border of several natural and climatic zones. A significant part of the region's territory is characterized as a forest-steppe zone with a lot of natural and anthropogenic landscapes, accompanied by continental climate. It provides a rich diversity of natural vegetation and cultural associations. During last 10 years pollen grains has been monitored in the airspace of Barnaul city (the capital of Altai Krai) located in the central part of the forest-steppe zone). During the monitoring, the attempts to determine the origin of pollen spectra (local or introduced) were made as well. In the long-term average dates of the first wave of dusting in the spring season 2014 Burkard pollen traps were used in order to monitor the airspace in Barnaul, namely dry deposition of pollen grains [Nenasheva, 2013]. To estimate the wet deposition PBAP (pollen), which can reach 80% in the middle latitudes, precipitation sampler were installed close to Burkard pollen traps in order to sample precipitation. The samples were filtered through a filter having a pore diameter of 1 µm, then prepared and examined for the presence of pollen grains. The comparison of the results of pollen analysis of 10 samples

Atmospheric Nitrogen Deposition at Two Sites in an Arid Environment of Central Asia.

Science.gov (United States)

Li, Kaihui; Liu, Xuejun; Song, Wei; Chang, Yunhua; Hu, Yukun; Tian, Changyan

2013-01-01

Arid areas play a significant role in the global nitrogen cycle. Dry and wet deposition of inorganic nitrogen (N) species were monitored at one urban (SDS) and one suburban (TFS) site at Urumqi in a semi-arid region of central Asia. Atmospheric concentrations of NH3, NO2, HNO3, particulate ammonium and nitrate (pNH4 (+) and pNO3 (-)) concentrations and NH4-N and NO3-N concentrations in precipitation showed large monthly variations and averaged 7.1, 26.6, 2.4, 6.6, 2.7 µg N m(-3) and 1.3, 1.0 mg N L(-1) at both SDS and TFS. Nitrogen dry deposition fluxes were 40.7 and 36.0 kg N ha(-1) yr(-1) while wet deposition of N fluxes were 6.0 and 8.8 kg N ha(-1) yr(-1) at SDS and TFS, respectively. Total N deposition averaged 45.8 kg N ha(-1) yr(-1)at both sites. Our results indicate that N dry deposition has been a major part of total N deposition (83.8% on average) in an arid region of central Asia. Such high N deposition implies heavy environmental pollution and an important nutrient resource in arid regions.

Analysis of Co, Cr and Mn Concentrations in Atmospheric Dry Deposition in Hamadan City

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P. Shokri Ragheb

2016-07-01

Full Text Available Introduction & Objective: Heavy metals are major pollutants that can spread in the atmosphere with particulate matter and dust and because of the toxic and carcinogenic effects, their meas-urement and control is very important. Therefore, this study was conducted to assess Co, Cr and Mn concentration in the atmospheric dry deposition collected from Hamadan city in 2014. Materials & Methods: After collection of 12 dust samples from 3 sampling stations and their laboratory preparation, metals concentrations were determined using ICP–OES. All statistical analyses were performed using the SPSS statistical package. Results: The results showed that the minimum and maximum mean concentrations of Co were 0.19 and 0.29 mg/kg for high and low traffic intensity sampling stations, respectively. The min and max mean concentrations of Cr were 0.65and 1.02 mg/kg for high traffic intensity and suburb sampling stations, respectively and the min and max mean concentrations of Mn were 7.23and 8.82 mg/kg for high and low traffic intensity sampling stations , respectively. Also comparing the mean concentrations of assessed metals with WHO permissible limits showed a significant difference (P< 0.05. The mean concentrations of metals were signifi-cantly lower than the maximum permissible limits. Conclusion: Although the mean concentrations of Co, Cr and Mn are lower than the standard levels, lack of continuous monitoring of heavy metals concentrations in the dust and particu-late matters in the air can lead to the entrance of various types of toxic pollutants such as heavy metals into the air and result in adverse health effects. (Sci J Hamadan Univ Med Sci 2016; 23 (2:149-156

Dry deposition on urban surfaces

International Nuclear Information System (INIS)

Roed, J.

1985-01-01

In order to facilitate developing a model for deposition in urban areas, beryllium-7, created by cosmic radiation and fall-out cesium-137, have been used as tracers in measurements designed to find the dry deposition velocity on building surfaces. A literature review has revealed that very little work has been done on deposition in urban areas; therefore, a major effort on meausring the deposition parameter is needed to construct reliable models in this field. Deposition velocities in the range from 0.001-0.04 cm/s have been found. (author)

Atmospheric mercury deposition and its contribution of the regional atmospheric transport to mercury pollution at a national forest nature reserve, southwest China.

Science.gov (United States)

Ma, Ming; Wang, Dingyong; Du, Hongxia; Sun, Tao; Zhao, Zheng; Wei, Shiqing

2015-12-01

Atmospheric mercury deposition by wet and dry processes contributes to the transformation of mercury from atmosphere to terrestrial and aquatic systems. Factors influencing the amount of mercury deposited to subtropical forests were identified in this study. Throughfall and open field precipitation samples were collected in 2012 and 2013 using precipitation collectors from forest sites located across Mt. Jinyun in southwest China. Samples were collected approximately every 2 weeks and analyzed for total (THg) and methyl mercury (MeHg). Forest canopy was the primary factor on THg and MeHg deposition. Simultaneously, continuous measurements of atmospheric gaseous elemental mercury (GEM) were carried out from March 2012 to February 2013 at the summit of Mt. Jinyun. Atmospheric GEM concentrations averaged 3.8 ± 1.5 ng m(-3), which was elevated compared with global background values. Sources identification indicated that both regional industrial emissions and long-range transport of Hg from central, northeast, and southwest China were corresponded to the elevated GEM levels. Precipitation deposition fluxes of THg and MeHg in Mt. Jinyun were slightly higher than those reported in Europe and North America, whereas total fluxes of MeHg and THg under forest canopy on Mt. Jiuyun were 3 and 2.9 times of the fluxes of THg in wet deposition in the open. Highly elevated litterfall deposition fluxes suggest that even in remote forest areas of China, deposition of atmospheric Hg(0) via uptake by vegetation leaf may be a major pathway for the deposition of atmospheric Hg. The result illustrates that areas with greater atmospheric pollution can be expected to have greater fluxes of Hg to soils via throughfall and litterfall.

Aerosol dynamics within and above forest in relation to turbulent transport and dry deposition

Directory of Open Access Journals (Sweden)

Ü. Rannik

2016-03-01

Full Text Available A 1-D atmospheric boundary layer (ABL model coupled with a detailed atmospheric chemistry and aerosol dynamical model, the model SOSAA, was used to predict the ABL and detailed aerosol population (characterized by the number size distribution time evolution. The model was applied over a period of 10 days in May 2013 to a pine forest site in southern Finland. The period was characterized by frequent new particle formation events and simultaneous intensive aerosol transformation. The aim of the study was to analyze and quantify the role of aerosol and ABL dynamics in the vertical transport of aerosols. It was of particular interest to what extent the fluxes above the canopy deviate from the particle dry deposition on the canopy foliage due to the above-mentioned processes. The model simulations revealed that the particle concentration change due to aerosol dynamics frequently exceeded the effect of particle deposition by even an order of magnitude or more. The impact was, however, strongly dependent on particle size and time. In spite of the fact that the timescale of turbulent transfer inside the canopy is much smaller than the timescales of aerosol dynamics and dry deposition, leading us to assume well-mixed properties of air, the fluxes at the canopy top frequently deviated from deposition inside the forest. This was due to transformation of aerosol concentration throughout the ABL and resulting complicated pattern of vertical transport. Therefore we argue that the comparison of timescales of aerosol dynamics and deposition defined for the processes below the flux measurement level do not unambiguously describe the importance of aerosol dynamics for vertical transport above the canopy. We conclude that under dynamical conditions reported in the current study the micrometeorological particle flux measurements can significantly deviate from the dry deposition into the canopy. The deviation can be systematic for certain size ranges so that the

Isotope studies to determine dry deposition of sulfate to deciduous and coniferous trees: Final draft

International Nuclear Information System (INIS)

Garten, C.T. Jr.

1988-01-01

Experiments have been conducted at two locations near Oak Ridge, Tennessee, with radioactive 35 S (87 day half-life) to examine the cycling behavior of sulfur in yellow poplar (Liriodendron tulipifera), red maple (Acer rubrum), and loblolly pine (Pinus taeda) trees. Some findings pertain to methods development for estimating dry deposition of sulfur to forest canopies and the magnitude of sulfur emissions from natural sources (Task II). We will determine through field studies, the internal cycling, storage, and biogenic emission of sulfur, as traced by 35 SO 4 2- , in environments impacted by atmospheric sulfate deposition; and will determine through isotope dilution studies, the contribution of foliar leaching and dry deposition to net throughfall (NTF) sulfate concentrations beneath deciduous and coniferous trees in such environments. 3 refs., 2 figs., 1 tab

Chemical Controls of Ozone Dry Deposition to the Sea Surface Microlayer

Science.gov (United States)

Carpenter, L.; Chance, R.; Tinel, L.; Saint, A.; Sherwen, T.; Loades, D.; Evans, M. J.; Boxhall, P.; Hamilton, J.; Stolle, C.; Wurl, O.; Ribas-Ribas, M.; Pereira, R.

2017-12-01

Oceanic dry deposition of atmospheric ozone (O3) is both the largest and most uncertain O3 depositional sink, and is widely acknowledged to be controlled largely by chemical reactions in the sea surface microlayer (SML) involving iodide (I-) and dissolved organic material (DOM). These reactions not only determine how quickly O3 can be removed from the atmosphere, but also result in emissions of trace gases including volatile organic compounds and may constitute a source of secondary organic aerosols to the marine atmosphere. Iodide concentrations at the sea surface vary by approximately an order of magnitude spatially, leading to more than fivefold variation in ozone deposition velocities (and volatile iodine fluxes). Sea-surface temperature is a reasonable predictor of [I-], however two recent parameterisations for surface I- differ by a factor of two at low latitudes. The nature and reactivity of marine DOM to O3 is almost completely unknown, although studies have suggested approximately equivalent chemical control of I- and DOM on ozone deposition. Here we present substantial new measurements of oceanic I- in both bulk seawater and the overlying SML, and show improved estimates of the global sea surface iodide distribution. We also present analyses of water-soluble DOM isolated from the SML and bulk seawater, and corresponding laboratory studies of ozone uptake to bulk and SML seawater, with the aim of characterizing the reactivity of O3 towards marine DOM.

Atmospheric Deposition: Sampling Procedures, Analytical Methods, and Main Recent Findings from the Scientific Literature

Directory of Open Access Journals (Sweden)

M. Amodio

2014-01-01

Full Text Available The atmosphere is a carrier on which some natural and anthropogenic organic and inorganic chemicals are transported, and the wet and dry deposition events are the most important processes that remove those chemicals, depositing it on soil and water. A wide variety of different collectors were tested to evaluate site-specificity, seasonality and daily variability of settleable particle concentrations. Deposition fluxes of POPs showed spatial and seasonal variations, diagnostic ratios of PAHs on deposited particles, allowed the discrimination between pyrolytic or petrogenic sources. Congener pattern analysis and bulk deposition fluxes in rural sites confirmed long-range atmospheric transport of PCDDs/Fs. More and more sophisticated and newly designed deposition samplers have being used for characterization of deposited mercury, demonstrating the importance of rain scavenging and the relatively higher magnitude of Hg deposition from Chinese anthropogenic sources. Recently biological monitors demonstrated that PAH concentrations in lichens were comparable with concentrations measured in a conventional active sampler in an outdoor environment. In this review the authors explore the methodological approaches used for the assessment of atmospheric deposition, from the analysis of the sampling methods, the analytical procedures for chemical characterization of pollutants and the main results from the scientific literature.

Short-term variability of 7Be atmospheric deposition and watershed response in a Pacific coastal stream, Monterey Bay, California, USA

Science.gov (United States)

Conaway, Christopher H.; Storlazzi, Curt D.; Draut, Amy E.; Swarzenski, Peter W.

2013-01-01

Beryllium-7 is a powerful and commonly used tracer for environmental processes such as watershed sediment provenance, soil erosion, fluvial and nearshore sediment cycling, and atmospheric fallout. However, few studies have quantified temporal or spatial variability of 7Be accumulation from atmospheric fallout, and parameters that would better define the uses and limitations of this geochemical tracer. We investigated the abundance and variability of 7Be in atmospheric deposition in both rain events and dry periods, and in stream surface-water samples collected over a ten-month interval at sites near northern Monterey Bay (37°N, 122°W) on the central California coast, a region characterized by a rainy winters, dry summers, and small mountainous streams with flashy hydrology. The range of 7Be activity in rainwater samples from the main sampling site was 1.3–4.4 Bq L−1, with a mean (±standard deviation) of 2.2 ± 0.9 Bq L−1, and a volume-weighted average of 2.0 Bq L−1. The range of wet atmospheric deposition was 18–188 Bq m−2 per rain event, with a mean of 72 ± 53 Bq m−2. Dry deposition fluxes of 7Be ranged from less than 0.01 up to 0.45 Bq m−2 d−1, with an estimated dry season deposition of 7 Bq m−2 month−1. Annualized 7Be atmospheric deposition was approximately 1900 Bq m−2 yr−1, with most deposition via rainwater (>95%) and little via dry deposition. Overall, these activities and deposition fluxes are similar to values found in other coastal locations with comparable latitude and Mediterranean-type climate. Particulate 7Be values in the surface water of the San Lorenzo River in Santa Cruz, California, ranged from −1 to 0.6 Bq g−1, with a median activity of 0.26 Bq g−1. A large storm event in January 2010 characterized by prolonged flooding resulted in the entrainment of 7Be-depleted sediment, presumably from substantial erosion in the watershed. There were too few particulate 7Be data over the storm to accurately model a 7Be load

Forest condition and chemical characteristics of atmospheric depositions: research and monitoring network in Lombardy

Directory of Open Access Journals (Sweden)

Flaminio DI GIROLAMO

2002-09-01

Full Text Available Since 1987, the Regional Forestry Board of Lombardy and the Water Research Institute of the National Research Council have been carrying out surveys of forest conditions and the response of the ecosystem to environmental factors. The study approach is based on a large number of permanent plots for extensive monitoring (Level 1. At this level, crown condition is assessed annually, and soil condition and the nutritional status of forests surveyed. Some of the permanent plots were selected for intensive monitoring (Level 2, focussing mainly on the impact of atmospheric pollution on forest ecosystems. Level 2 monitoring also includes increment analyses, ground vegetation assessment, atmospheric deposition, soil solution analyses and climatic observations. This paper summarises the main results of a pluriannual research, which provides a general picture of the state of forest health in the region and focuses on more detailed investigations, described as case studies. Modified wet and dry samplers which use a water surface to collect dry deposition were used in a pluriannual field campaign at five sites in alpine and prealpine areas, to measure the total atmospheric depositions and to evaluate the nitrogen and sulphate exceedances of critical loads. Throughfall and bulk precipitation chemistry were studied for five years (June 1994-May 1999 at two high elevation forest sites (Val Gerola and Val Masino which were known to differ in terms of tree health, as assessed by live crown condition. Results indicated a higher contribution from the dry deposition of N-NO3 -, N-NH4 + and H+ and considerable canopy leaching of Ca2+, K+ and weak organic acids at Val Gerola, where the symptoms of damage were more evident. In the area of Val Masino (SO, included since 1997 in the national CONECOFOR network, investigations focused on the effectiveness of the biological compartment in modifying fluxes of atmospheric elements, and on the role of nitrogen both as an

Atmospheric heavy metal deposition in the Copenhagen area

Energy Technology Data Exchange (ETDEWEB)

Andersen, A; Hovmand, M F; Johnsen, I

1978-10-01

Transport of heavy metals from the atmosphere to the soil and vegetation takes place by dust fall, bulk precipitation, and gas/aerosol adsorption processes. Atmospheric dry and wet deposition of the heavy metals lead, zinc, nickel, vanadium, iron, and copper over the Copenhagen area was measured by sampling in plastic funnels from 17 stations throughout the area for 12 months. Epigeic bryophytes, epiphytic lichen, and topsoil samples were analyzed. A linear correlation between bulk precipitation and heavy metal concentration in lichens and bryophytes was found. An exponential correlation between bulk precipitation and heavy metal concentration in soil was noted. Regional variation of the heavy metal levels in the Copenhagen area was described, and three sub-areas with high metal burdens were distinguished. (10 diagrams, 8 graphs, 13 references, 2 tables)

Measurements of dry-deposition parameters for the California acid-deposition monitoring program. Final report

International Nuclear Information System (INIS)

Watson, J.G.; Chow, J.C.; Egami, R.T.; Bowen, J.L.; Frazier, C.A.

1991-06-01

The State of California monitors the concentrations of acidic gases and particles at 10 sites throughout the state. Seven sites represent urban areas (South Coast Air Basin - three sites, San Francisco Bay Area, Bakersfield, Santa Barbara, and Sacramento) and three represent forested areas (Sequoia National Park, Yosemite National Park, and Gasquet). Several sites are collocated with monitoring instruments for other air quality and forest response networks. Continuous monitors for the dry deposition network collect hourly average values for ozone, wind speed, wind direction, atmospheric stability, temperature, dew point, time of wetness, and solar radiation. A newly-designed gas/particle sampler collects daytime (6 a.m. to 6 p.m.) and nighttime (6 p.m. to 6 a.m.) samples every sixth day for sulfur dioxide, ammonia, nitrogen dioxide, and nitric acid. Particles are collected on the same day/night schedule in PM(10) and PM(2.5) size ranges, and are analyzed for mass, sulfate, nitrate, chloride, ammonium, sodium, magnesium, potassium, and calcium ions. The sampling schedule follows the regulatory schedule adopted by the EPA and ARB for suspended particulate matter. Wet deposition data are collected at or nearby the dry deposition stations. The first year of the monitoring program included installation of the network, training of technicians, acquisition and validation of data, and transfer of the sampling and analysis technology to Air Resources Board operating divisions. Data have been validated and stored for the period May, 1988 through September, 1989

Simulation of trace metals and PAH atmospheric pollution over Greater Paris: Concentrations and deposition on urban surfaces

Science.gov (United States)

Thouron, L.; Seigneur, C.; Kim, Y.; Legorgeu, C.; Roustan, Y.; Bruge, B.

2017-10-01

Urban areas can be subject not only to poor air quality, but also to contamination of other environmental media by air pollutants. Here, we address the potential transfer of selected air pollutants (two metals and three PAH) to urban surfaces. To that end, we simulate meteorology and air pollution from Europe to a Paris suburban neighborhood, using a four-level one-way nesting approach. The meteorological and air quality simulations use urban canopy sub-models in order to better represent the effect of the urban morphology on the air flow, atmospheric dispersion, and deposition of air pollutants to urban surfaces. This modeling approach allows us to distinguish air pollutant deposition among various urban surfaces (roofs, roads, and walls). Meteorological model performance is satisfactory, showing improved results compared to earlier simulations, although precipitation amounts are underestimated. Concentration simulation results are also satisfactory for both metals, with a fractional bias Paris region. The model simulation results suggest that both wet and dry deposition processes need to be considered when estimating the transfer of air pollutants to other environmental media. Dry deposition fluxes to various urban surfaces are mostly uniform for PAH, which are entirely present in fine particles. However, there is significantly less wall deposition compared to deposition to roofs and roads for trace metals, due to their coarse fraction. Meteorology, particle size distribution, and urban morphology are all important factors affecting air pollutant deposition. Future work should focus on the collection of data suitable to evaluate the performance of atmospheric models for both wet and dry deposition with fine spatial resolution.

Dual Nitrate Isotopes in Dry Deposition: Utility for Partitioning Nox Source Contributions to Landscape Nitrogen Deposition

Science.gov (United States)

Dry deposition is a major component of total nitrogen deposition and thus an important source of bioavailable nitrogen to ecosystems. However, relative to wet deposition, less is known regarding the sources and spatial variability of dry deposition. This is in part due to diffi...

Dry deposition and fate of radionuclides within spruce canopies

International Nuclear Information System (INIS)

Ould-Dada, Z.; Shaw, G.; Kinnersley, R.P.; Minski, M.J.

1997-01-01

The assessment of radiation dose to human populations from the release of radionuclides into the atmosphere following a nuclear accident relies on the use of simulation models. These need to be calibrated and tested using experimental data. In this study, the deposition and resuspension of radionuclides within a forest environment was investigated. Forests were identified in the aftermath of the Chernobyl accident as a specific type of semi-natural ecosystem for which radiological data were lacking within the countries of the European Union. Wind tunnel and field data have been collected for small model canopies of Norwegian spruce saplings using uranium and silica aerosol particles. These have provided quantitative estimates of the potential of a tree canopy to constitute an airborne inhalation hazard and a secondary source of airborne contamination after the initial deposition. Using these results, a multi-layer compartmental model of aerosol flux (CANDEP) has been developed and calibrated. It combines the processes of dry deposition, resuspension and field loss in individual layers of the model canopy. (5 figures; 4 tables; 15 references). (UK)

Dry deposition of gaseous radioiodine and particulate radiocaesium onto leafy vegetables

International Nuclear Information System (INIS)

Tschiersch, Jochen; Shinonaga, Taeko; Heuberger, Heidi

2009-01-01

Radionuclides released to the atmosphere during dry weather (e.g. after a nuclear accident) may contaminate vegetable foods and cause exposure to humans via the food chain. To obtain experimental data for an appropriate assessment of this exposure path, dry deposition of radionuclides to leafy vegetables was studied under homogeneous and controlled greenhouse conditions. Gaseous 131 I-tracer in predominant elemental form and particulate 134 Cs-tracer at about 1 μm diameter were used to identify susceptible vegetable species with regard to contamination by these radionuclides. The persistence was examined by washing the harvested product with water. The vegetables tested were spinach (Spinacia oleracea), butterhead lettuce (Lactuca sativa var. capitata), endive (Cichorium endivia), leaf lettuce (Lactuca sativa var. crispa), curly kale (Brassica oleracea convar. acephala) and white cabbage (Brassica oleracea convar. capitata). The variation of radionuclides deposited onto each vegetable was evaluated statistically using the non-parametric Kruskal-Wallis Test and the U-test of Mann-Whitney. Significant differences in deposited 131 I and 134 Cs activity concentration were found among the vegetable species. For 131 I, the deposition velocity to spinach normalized to the biomass of the vegetation was 0.5-0.9 cm 3 g -1 s -1 which was the highest among all species. The particulate 134 Cs deposition velocity of 0.09 cm 3 g -1 s -1 was the highest for curly kale, which has rough and structured leaves. The lowest deposition velocity was onto white cabbage: 0.02 cm 3 g -1 s -1 (iodine) and 0.003 cm 3 g -1 s -1 (caesium). For all species, the gaseous iodine deposition was significantly higher compared to the particulate caesium deposition. The deposition depends on the sensitive parameters leaf area, stomatal aperture, and plant morphology. Decontamination by washing with water was very limited for iodine but up to a factor of two for caesium.

Dry deposition models for radionuclides dispersed in air: a new approach for deposition velocity evaluation schema

Science.gov (United States)

Giardina, M.; Buffa, P.; Cervone, A.; De Rosa, F.; Lombardo, C.; Casamirra, M.

2017-11-01

In the framework of a National Research Program funded by the Italian Minister of Economic Development, the Department of Energy, Information Engineering and Mathematical Models (DEIM) of Palermo University and ENEA Research Centre of Bologna, Italy are performing several research activities to study physical models and mathematical approaches aimed at investigating dry deposition mechanisms of radioactive pollutants. On the basis of such studies, a new approach to evaluate the dry deposition velocity for particles is proposed. Comparisons with some literature experimental data show that the proposed dry deposition scheme can capture the main phenomena involved in the dry deposition process successfully.

Atmospheric deposition as a source of carbon and nutrients to an alpine catchment of the Colorado Rocky Mountains

Science.gov (United States)

Mladenov, N.; Williams, M. W.; Schmidt, S. K.; Cawley, K.

2012-08-01

illustrated that wet deposition (9.9 kg C ha-1 yr-1) and dry deposition (6.9 kg C ha-1 yr-1) were a combined input of approximately 17 kg C ha-1 yr-1, which could be as high as 24 kg C ha-1 yr-1 in high dust years. This atmospheric C input approached the C input from microbial autotrophic production in barren soils. Atmospheric wet and dry deposition also contributed 4.3 kg N ha-1 yr-1, 0.15 kg P ha-1 yr-1, and 2.7 kg Ca2+ ha-1 yr-1 to this alpine catchment.

Even low to medium nitrogen deposition impacts vegetation of dry, coastal dunes around the Baltic Sea

International Nuclear Information System (INIS)

Remke, Eva; Brouwer, Emiel; Kooijman, Annemieke; Blindow, Irmgard; Esselink, Hans; Roelofs, Jan G.M.

2009-01-01

Coastal dunes around the Baltic Sea have received small amounts of atmospheric nitrogen and are rather pristine ecosystems in this respect. In 19 investigated dune sites the atmospheric wet nitrogen deposition is 3-8 kg N ha -1 yr -1 . The nitrogen content of Cladonia portentosa appeared to be a suitable biomonitor of these low to medium deposition levels. Comparison with EMEP-deposition data showed that Cladonia reflects the deposition history of the last 3-6 years. With increasing nitrogen load, we observed a shift from lichen-rich short grass vegetation towards species-poor vegetation dominated by the tall graminoid Carex arenaria. Plant species richness per field site, however, does not decrease directly with these low to medium N deposition loads, but with change in vegetation composition. Critical loads for acidic, dry coastal dunes might be lower than previously thought, in the range of 4-6 kg N ha -1 yr -1 wet deposition. - Even low to medium nitrogen deposition impacts Baltic dune vegetation promoting a dominance of taller graminoids

Sampling of Atmospheric Precipitation and Deposits for Analysis of Atmospheric Pollution

OpenAIRE

Skarżyńska, K.; Polkowska, Ż; Namieśnik, J.

2006-01-01

This paper reviews techniques and equipment for collecting precipitation samples from the atmosphere (fog and cloud water) and from atmospheric deposits (dew, hoarfrost, and rime) that are suitable for the evaluation of atmospheric pollution. It discusses the storage and preparation of samples for analysis and also presents bibliographic information on the concentration ranges of inorganic and organic compounds in the precipitation and atmospheric deposit samples.

Deposition of aerosols formed by HCDA due to decay heat transport in inner containment atmospheres

International Nuclear Information System (INIS)

Vate, J.F. van de

1976-01-01

Coupling of decay heat transfer by aerosol-laden inner containment atmospheres with aerosol deposition from such atmospheres leads to useful and simple models for calculation of the time dependence of the aerosol mass concentration. Special attention is given to thermophoretic deposition (dry case) and condensation followed by gravitational deposition (wet case). Attractive features of the models are: 1) coagulation can be omitted and therefore complicated and doubtful calculations on coagulation are avoided, 2) material and particle size of the aerosol are not important for the aerosol decay rate, 3) the aerosol decay rate is related to the decay heat production which is known function of time, and the relevant part of it must be assessed usually for other purposes as well. (orig.) [de

Atmospheric dry deposition in the vicinity of the Salton Sea, California - II: Measurement and effects of an enhanced evaporation system

Science.gov (United States)

Alonso, R.; Bytnerowicz, A.; Yee, J.L.; Boarman, W.I.

2005-01-01

A study was conducted to determine the effects of salt spray drift from pilot technologies employed by the US Bureau of Reclamation on deposition rates of various air-born ions. An enhanced evaporation system (EES) was tested in the field at the Salton Sea, California. Dry deposition of NO3-, NH4+, SO42-, Cl-, Ca2+, Na+, K+ and Se was assessed by using nylon filters and branches of natural vegetation exposed for one-week long periods. The simultaneous exposure of both lyophilized branches and branches of live plants offered important information highlighting the dynamics of deposited ions on vegetation. The EES significantly increased the deposition rates of Cl-, SO42- and Na+ in an area of about 639-1062 m surrounding the sprayers. Similarly, higher deposition of Ca 2+ and K+ caused by the EES was detected only when deposition was assessed using nylon filters or lyophilized branches. Deposition fluxes of NO3-, NH4+ and Se were not affected by the spraying system. Techniques for measuring dry deposition and calculating landscape-level depositional loads in non-forested systems need further development. ?? 2005 Elsevier Ltd. All rights reserved.

A revised global ozone dry deposition estimate based on a new two-layer parameterisation for air-sea exchange and the multi-year MACC composition reanalysis

Science.gov (United States)

Luhar, Ashok K.; Woodhouse, Matthew T.; Galbally, Ian E.

2018-03-01

Dry deposition at the Earth's surface is an important sink of atmospheric ozone. Currently, dry deposition of ozone to the ocean surface in atmospheric chemistry models has the largest uncertainty compared to deposition to other surface types, with implications for global tropospheric ozone budget and associated radiative forcing. Most global models assume that the dominant term of surface resistance in the parameterisation of ozone dry deposition velocity at the oceanic surface is constant. There have been recent mechanistic parameterisations for air-sea exchange that account for the simultaneous waterside processes of ozone solubility, molecular diffusion, turbulent transfer, and first-order chemical reaction of ozone with dissolved iodide and other compounds, but there are questions about their performance and consistency. We present a new two-layer parameterisation scheme for the oceanic surface resistance by making the following realistic assumptions: (a) the thickness of the top water layer is of the order of a reaction-diffusion length scale (a few micrometres) within which ozone loss is dominated by chemical reaction and the influence of waterside turbulent transfer is negligible; (b) in the water layer below, both chemical reaction and waterside turbulent transfer act together and are accounted for; and (c) chemical reactivity is present through the depth of the oceanic mixing layer. The new parameterisation has been evaluated against dry deposition velocities from recent open-ocean measurements. It is found that the inclusion of only the aqueous iodide-ozone reaction satisfactorily describes the measurements. In order to better quantify the global dry deposition loss and its interannual variability, modelled 3-hourly ozone deposition velocities are combined with the 3-hourly MACC (Monitoring Atmospheric Composition and Climate) reanalysis ozone for the years 2003-2012. The resulting ozone dry deposition is found to be 98.4 ± 30.0 Tg O3 yr-1 for the ocean

Atmospheric Deposition of Pb, Zn, Cu, and Cd in Amman, Jordan

International Nuclear Information System (INIS)

Momani, K.A.; Jiries, A.G.; Jaradat, Q.M.

1999-01-01

Atmospheric samples were collected by high-volume air sampler and dust fall containers during the summer of 1995 at different sites in Amman City, Jordan. Heavy metal contents in settle able (dust fall) as well as in air particulates (suspended) were analyzed by graphite furnace atomic absorption spectrophotometry. The atmospheric concentrations of Zn, Cu, Pb, and Cd were 344, 170, 291, and 3.8 ng/m 3 , respectively. On the other hand, the levels of these elements in dust fall deposition were 505, 94, 74, and 3.1 μg/g, respectively. The fluxes and dry deposition velocities of these heavy metals were determined and compared with the findings of other investigators worldwide. Significant enrichment coefficients of heavy metals in dust fall were observed. The enrichment coefficients were 12.1, 6.1, 11.7, and 1.1 for Zn, Cu, Pb, and Cd, respectively

A measurement of summertime dry deposition of ambient air particulates and associated metallic pollutants in Central Taiwan.

Science.gov (United States)

Fang, Guor-Cheng; Chiang, Hung-Che; Chen, Yu-Cheng; Xiao, You-Fu; Wu, Chia-Ming; Kuo, Yu-Chen

2015-04-01

The purpose of this study is to characterize metallic elements associated with atmospheric particulate matter in the dry deposition plate, total suspended particulate, fine particles, and coarse particles at Taichung Harbor and Gong Ming Junior High School (airport) in central Taiwan at a sampling site from June 2013 to August 2013. The results indicated that: (1) the average concentrations of the metallic elements Cr and Cd were highest at the Gong Ming Junior High School (airport), and the average concentrations of the metallic elements Ni, Cu, and Pb were highest at the Taichung Harbor sampling site. (2) The high smelting industry density and export/import rate of heavily loaded cargos were the main reasons leading to these findings. (3) The average metallic element dry deposition and metallic element PM(2.5-10) all followed the order of Pb > Cr > Cu > Ni > Cd at the two sampling sites. However, the average metallic elements Cu and Pb were found to have the highest dry deposition velocities and concentrations in PM(2.5) for the two sampling sites in this study. (4) The correlation coefficients of ambient air particle dry deposition and concentration with wind speed at the airport were higher than those from the harbor sampling site. The wind and broad open spaces at Taichung Airport were the possible reasons for the increasing correlation coefficients for ambient air particle concentration and dry deposition with wind speed at the Taichung Airport sampling site.

Dry-spray deposition of TiO2 for a flexible dye-sensitized solar cell (DSSC) using a nanoparticle deposition system (NPDS).

Science.gov (United States)

Kim, Min-Saeng; Chun, Doo-Man; Choi, Jung-Oh; Lee, Jong-Cheon; Kim, Yang Hee; Kim, Kwang-Su; Lee, Caroline Sunyong; Ahn, Sung-Hoon

2012-04-01

TiO2 powders were deposited on indium tin oxide (ITO) coated polyethylene terephthalate (PET) substrates for application to the photoelectrode of a dye-sensitized solar cell (DSSC). In the conventional DSSC manufacturing process, a semiconductor oxide such as TiO2 powder requires a sintering process at higher temperature than the glass transition temperature (T(g)) of polymers, and thus utilization of flexible polymer substrates in DSSC research has been constrained. To overcome this restriction related to sintering, we used a nanoparticle deposition system (NPDS) that could produce a thin coating layer through a dry-spray method under atmospheric pressure at room temperature. The powder was sprayed through a slit-type nozzle having a 0.4 x 10 mm2 rectangular outlet. In order to determine the deposited TiO2 thickness, five kinds of TiO2 layered specimens were prepared, where the specimens have single and double layer structures. Deposited powders on the ITO coated PET substrates were observed using FE-SEM and a scan profiler The thicker TiO2 photoelectrode with a DSSC having a double layer structure showed higher energy efficiency than the single layer case. The highest fabricated flexible DSSC displayed a short circuit current density J(sc) = 1.99 mA cm(-2), open circuit voltage V(oc) = 0.71 V, and energy efficiency eta = 0.94%. These results demonstrate the possibility of utilizing the dry-spray method to fabricate a TiO2 layer on flexible polymer substrates at room temperature under atmospheric pressure.

Measurements of dry-deposition rates on various earth surfaces by 212Pb

International Nuclear Information System (INIS)

Osaki, S.; Sugihara, S.; Maeda, Y.

2004-01-01

Dry deposition rates of 212 Pb on a coniferous forest (Japanese cedar) and a broad-leaf forest (Pasania edulis) have been measured. Those on various kinds of grass fields, various states on artificial surface such as water, paper, and standing paper have been also measured. The dry deposition rates depend on the characteristics of depositing particles and the conditions of deposited surfaces. Dry deposition rates on the forest of Japanese cedar are highest because of the complex and adhesive surface of the leaves. Those on various grass fields are roughly depend on the logarithm of the height of their grasses. The total deposition rates of 7 Be do not depend on the densities or heights of the grasses. 7 Be may be not kept on their leaves or surface soil for a long time. The dry deposition rates of on artificial surface, e.g. paper and water surfaces make clear the mechanism on dry deposition, and suggest that more chances of collision and more adhesive of the surface are important for the dry deposition. About 90% of all deposition on the artificial paper grass was attached on the standing paper. On water surface, 60% of the rate of paper grass was attached, but only about 20% were attached on a dry paper plate. The aerosol particles are deposited by collision with the surface, therefore the deposition velocity depends on the chance of collision and the characteristics of the surface. Therefore the dry deposition rates on forests are larger and those of coniferous forest are largest. (author)

Monitoring the dry deposition of SO2 in the Netherlands

NARCIS (Netherlands)

Erisman JW; Versluis AH; Verplanke TAJW; Haan D de; Anink D; Elzakker BG van; Aalst RM van

1989-01-01

A micrometeorological gradient method has been applied to monitor SO2 dry deposition fluxes on a routine basis. Results of a feasibility study during 1987 to 1989 at a rural site in the Netherlands demonstrated that this method can be used to measure dry deposition flux and deposition velocity

Equipment selection for atmospheric drying

Energy Technology Data Exchange (ETDEWEB)

Sharma, P D; Bhattacharyya, S [Nuclear Power Corporation, Bhabha Atomic Research Centre, Mumbai (India)

1994-06-01

Heavy water management is a major factor in deciding the economics of the PHWRs. Hence it is necessary to have an efficient recovery system, for the heavy water vapour escaping from various process systems and maintain a dry atmosphere in the recovery areas. While the basic objective of the atmospheric drying system is to maximize recovery and to minimize stack losses, it is equally important to optimally design the system with due consideration to operational and maintenance aspects. At present, heavy water vapour recovery in the existing Nuclear Power Plants (NPPs) is carried out by dryers of dual fixed bed design. While moving bed design could have some advantages, this has not been adopted so far because of the cumbersome mechanical design involved and special requirements for nuclear application. Developmental work done in this direction has resulted in compact alternative designs. In one of the designs, the change over from adsorption to regeneration is achieved by rotating the bed slowly. This concept is further refined in another alternative using a dessicant wheel. This paper contains brief equipment description of different designs; enumerates the design requirements of an atmospheric drying system for reactor building; describes steps for designing fixed bed type D{sub 2}O vapour recovery system, and highlights advances in dryer technology. (author). 2 refs., 4 figs., 1 ill.

Acid Deposition Phenomena

International Nuclear Information System (INIS)

Ramadan, A.E.K.

2004-01-01

Acid deposition, commonly known as acid rain, occurs when emissions from the combustion of fossil fuels and other industrial processes undergo complex chemical reactions in the atmosphere and fall to the earth as wet deposition (rain, snow, cloud, fog) or dry deposition (dry particles, gas). Rain and snow are already naturally acidic, but are only considered problematic when less than a ph of 5.0 The main chemical precursors leading to acidic conditions are atmospheric concentrations of sulfur dioxide (SO 2 ) and nitrogen oxides (NO x ). When these two compounds react with water, oxygen, and sunlight in the atmosphere, the result is sulfuric (H 2 SO 4 ) and nitric acids (HNO 3 ), the primary agents of acid deposition which mainly produced from the combustion of fossil fuel and from petroleum refinery. Airborne chemicals can travel long distances from their sources and can therefore affect ecosystems over broad regional scales and in locations far from the sources of emissions. According to the concern of petroleum ministry with the environment and occupational health, in this paper we will discussed the acid deposition phenomena through the following: Types of acidic deposition and its components in the atmosphere Natural and man-made sources of compounds causing the acidic deposition. Chemical reactions causing the acidic deposition phenomenon in the atmosphere. Factors affecting level of acidic deposition in the atmosphere. Impact of acid deposition. Procedures for acidic deposition control in petroleum industry

Atmospheric freeze drying assisted by power ultrasound

International Nuclear Information System (INIS)

Santacatalina, J V; Cárcel, J A; Garcia-Perez, J V; Mulet, A; Simal, S

2012-01-01

Atmospheric freeze drying (AFD) is considered an alternative to vacuum freeze drying to keep the quality of fresh product. AFD allows continuous drying reducing fix and operating costs, but presents, as main disadvantage, a long drying time required. The application of power ultrasound (US) can accelerate AFD process. The main objective of the present study was to evaluate the application of power ultrasound to improve atmospheric freeze drying of carrot. For that purpose, AFD experiments were carried out with carrot cubes (10 mm side) at constant air velocity (2 ms −1 ), temperature (−10°C) and relative humidity (10%) with (20.5 kWm −3 ,USAFD) and without (AFD) ultrasonic application. A diffusion model was used in order to quantify the influence of US in drying kinetics. To evaluate the quality of dry products, rehydration capacity and textural properties were determined. The US application during AFD of carrot involved the increase of drying rate. The effective moisture diffusivity identified in USAFD was 73% higher than in AFD experiments. On the other hand, the rehydration capacity was higher in USAFD than in AFD and the hardness of dried samples did not show significant (p<0.05) differences. Therefore, US application during AFD significantly (p<0.05) sped-up the drying process preserving the quality properties of the dry product.

Atmospheric deposition 2000. NOVA 2003; Atmosfaerisk deposition 2000. NOVA 2003

Energy Technology Data Exchange (ETDEWEB)

Ellermann, T.; Hertel, O.; Hovmand, M.F.; Kemp, K.; Skjoeth, C.A.

2001-11-01

This report presents measurements and calculations from the atmospheric part of NOVA 2003 and covers results for 2000. It summarises the main results concerning concentrations and depositions of nitrogen, phosphorus and sulphur compounds related to eutrophication and acidification. Depositions of atmospheric compounds to Danish marine waters as well as land surface are presented. Measurements: In 2000 the monitoring program consisted of eight stations where wet deposition of ammonium, nitrate, phosphate (semi quantitatively) and sulphate were measured using bulk precipitation samplers. Six of the stations had in addition measurements of atmospheric content of A, nitrogen, phosphorus, and sulphur compounds in gas and particulate phase carried out by use of filter pack samplers. Filters were analysed at the National Environmental Research Institute. Furthermore nitrogen dioxide were measured using nitrogen dioxide filter samplers and monitors. Model calculations: The measurements in the monitoring program were supplemented with model calculations of concentrations and depositions of nitrogen and sulphur compounds to Danish land surface, marine waters, fjords and bays using the ACDEP model (Atmospheric Chemistry and Deposition). The model is a so-called trajectory model and simulates the physical and chemical processes in the atmosphere using meteorological and emission data as input. The advantage of combining measurements with model calculations is that the strengths of both methods is obtained. Conclusions concerning: 1) actual concentration levels at the monitoring stations, 2) deposition at the monitoring stations, 3) seasonal variations and 4) long term trends in concentrations and depositions are mainly based on the direct measurements. These are furthermore used to validate the results of the model calculations. Calculations and conclusions concerning: 1) depositions to land surface and to the individual marine water, 2) contributions from different emission

Achieving uniform layer deposition by atmospheric-pressure plasma-enhanced chemical vapor deposition

Energy Technology Data Exchange (ETDEWEB)

Lee, Jae-Ok [Department of Plasma Engineering, Korea Institute of Machinery & Materials (KIMM), Daejeon 305-343 (Korea, Republic of); Kang, Woo Seok, E-mail: kang@kimm.re.kr [Department of Plasma Engineering, Korea Institute of Machinery & Materials (KIMM), Daejeon 305-343 (Korea, Republic of); Department of Environment & Energy Mechanical Engineering, University of Science & Technology (UST), Daejeon 305-350 (Korea, Republic of); Hur, Min; Lee, Jin Young [Department of Plasma Engineering, Korea Institute of Machinery & Materials (KIMM), Daejeon 305-343 (Korea, Republic of); Song, Young-Hoon [Department of Plasma Engineering, Korea Institute of Machinery & Materials (KIMM), Daejeon 305-343 (Korea, Republic of); Department of Environment & Energy Mechanical Engineering, University of Science & Technology (UST), Daejeon 305-350 (Korea, Republic of)

2015-12-31

This work investigates the use of plasma-enhanced chemical vapor deposition under atmospheric pressure for achieving uniform layer formation. Electrical and optical measurements demonstrated that the counterbalance between oxygen and precursors maintained the homogeneous discharge mode, while creating intermediate species for layer deposition. Several steps of the deposition process of the layers, which were processed on a stationary stage, were affected by flow stream and precursor depletion. This study showed that by changing the flow streamlines using substrate stage motion uniform layer deposition under atmospheric pressure can be achieved. - Highlights: • Zirconium oxide was deposited by atmospheric-pressure plasma-enhanced chemical vapor deposition. • Homogeneous plasma was maintained by counterbalancing between discharge gas and precursors. • Several deposition steps were observed affected by the gas flow stream and precursor depletion. • Thin film layer was uniformly grown when the substrate underwent a sweeping motion.

Active moss biomonitoring of trace elements with Sphagnum girgensohnii moss bags in relation to atmospheric bulk deposition in Belgrade, Serbia

International Nuclear Information System (INIS)

Anicic, M.; Tasic, M.; Frontasyeva, M.V.; Tomasevic, M.; Rajsic, S.; Mijic, Z.; Popovic, A.

2009-01-01

Active biomonitoring with wet and dry moss bags was used to examine trace element atmospheric deposition in the urban area of Belgrade. The element accumulation capability of Sphagnum girgensohnii Russow was tested in relation to atmospheric bulk deposition. Moss bags were mounted for five 3-month periods (July 2005-October 2006) at three representative urban sites. For the same period monthly bulk atmospheric deposition samples were collected. The concentrations of Al, V, Cr, Mn, Fe, Ni, Cu, Zn, As, Cd, and Pb were determined by instrumental neutron activation analyses and atomic absorption spectrometry. Significant accumulation of most elements occurred in the exposed moss bags compared with the initial moss content. High correlations between the elements in moss and bulk deposits were found for V, Cu, As, and Ni. The enrichment factors of the elements for both types of monitor followed the same pattern at the corresponding sites. - Accumulated trace elements in the moss Sphagnum girgensohnii reflect atmospheric deposition

Dry deposition of gaseous radioiodine and particulate radiocaesium onto leafy vegetables

Energy Technology Data Exchange (ETDEWEB)

Tschiersch, Jochen, E-mail: tschiersch@helmholtz-muenchen.de [Helmholtz Zentrum Muenchen, German Research Center for Environmental Health, Institute of Radiation Protection, Ingolstaedter Landstr. 1, 85764 Neuherberg (Germany); Shinonaga, Taeko [Helmholtz Zentrum Muenchen, German Research Center for Environmental Health, Institute of Radiation Protection, Ingolstaedter Landstr. 1, 85764 Neuherberg (Germany); Heuberger, Heidi [TU Muenchen, Center of Life and Food Sciences Weihenstephan, Duernast 2, 85350 Freising (Germany)

2009-10-15

Radionuclides released to the atmosphere during dry weather (e.g. after a nuclear accident) may contaminate vegetable foods and cause exposure to humans via the food chain. To obtain experimental data for an appropriate assessment of this exposure path, dry deposition of radionuclides to leafy vegetables was studied under homogeneous and controlled greenhouse conditions. Gaseous {sup 131}I-tracer in predominant elemental form and particulate {sup 134}Cs-tracer at about 1 {mu}m diameter were used to identify susceptible vegetable species with regard to contamination by these radionuclides. The persistence was examined by washing the harvested product with water. The vegetables tested were spinach (Spinacia oleracea), butterhead lettuce (Lactuca sativa var. capitata), endive (Cichorium endivia), leaf lettuce (Lactuca sativa var. crispa), curly kale (Brassica oleracea convar. acephala) and white cabbage (Brassica oleracea convar. capitata). The variation of radionuclides deposited onto each vegetable was evaluated statistically using the non-parametric Kruskal-Wallis Test and the U-test of Mann-Whitney. Significant differences in deposited {sup 131}I and {sup 134}Cs activity concentration were found among the vegetable species. For {sup 131}I, the deposition velocity to spinach normalized to the biomass of the vegetation was 0.5-0.9 cm{sup 3} g{sup -1} s{sup -1} which was the highest among all species. The particulate {sup 134}Cs deposition velocity of 0.09 cm{sup 3} g{sup -1} s{sup -1} was the highest for curly kale, which has rough and structured leaves. The lowest deposition velocity was onto white cabbage: 0.02 cm{sup 3} g{sup -1} s{sup -1} (iodine) and 0.003 cm{sup 3} g{sup -1} s{sup -1} (caesium). For all species, the gaseous iodine deposition was significantly higher compared to the particulate caesium deposition. The deposition depends on the sensitive parameters leaf area, stomatal aperture, and plant morphology. Decontamination by washing with water was very

Evaluate dry deposition velocity of the nitrogen oxides using Noah-MP physics ensemble simulations for the Dinghushan Forest, Southern China

Science.gov (United States)

Zhang, Qi; Chang, Ming; Zhou, Shengzhen; Chen, Weihua; Wang, Xuemei; Liao, Wenhui; Dai, Jianing; Wu, ZhiYong

2017-11-01

There has been a rapid growth of reactive nitrogen (Nr) deposition over the world in the past decades. The Pearl River Delta region is one of the areas with high loading of nitrogen deposition. But there are still large uncertainties in the study of dry deposition because of its complex processes of physical chemistry and vegetation physiology. At present, the forest canopy parameterization scheme used in WRF-Chem model is a single-layer "big leaf" model, and the simulation of radiation transmission and energy balance in forest canopy is not detailed and accurate. Noah-MP land surface model (Noah-MP) is based on the Noah land surface model (Noah LSM) and has multiple parametric options to simulate the energy, momentum, and material interactions of the vegetation-soil-atmosphere system. Therefore, to investigate the improvement of the simulation results of WRF-Chem on the nitrogen deposition in forest area after coupled with Noah-MP model and to reduce the influence of meteorological simulation biases on the dry deposition velocity simulation, a dry deposition single-point model coupled by Noah- MP and the WRF-Chem dry deposition module (WDDM) was used to simulate the deposition velocity (Vd). The model was driven by the micro-meteorological observation of the Dinghushan Forest Ecosystem Location Station. And a series of numerical experiments were carried out to identify the key processes influencing the calculation of dry deposition velocity, and the effects of various surface physical and plant physiological processes on dry deposition were discussed. The model captured the observed Vd well, but still underestimated the Vd. The self-defect of Wesely scheme applied by WDDM, and the inaccuracy of built-in parameters in WDDM and input data for Noah-MP (e.g. LAI) were the key factors that cause the underestimation of Vd. Therefore, future work is needed to improve model mechanisms and parameterization.

Deposition rates of atmospheric particulates determined from 210Pb measurements in soils and air

International Nuclear Information System (INIS)

Likuku, A. S.; Branford, D.

2011-01-01

Deposition rates of atmospheric particles were determined using previously published 210P b data in soils and air. The dry deposition velocities for moorland and woodland soils were 2.2 ± 1.8 and 9 ± 2 mm · s - 1 , respectively. The 210P b concentration in rain was calculated to be 94 ± 10 mBq · L - 1. The large (∼ 4 times) deposition velocities in woodland relative to moorland soils is an indication of the degree of accumulation of particles, and most possibly contaminants within woodland soils, which is of practical importance in the mitigation of pollutant concentrations in urban areas by planting trees. (authors)

Lichen-based critical loads for atmospheric nitrogen deposition in Western Oregon and Washington Forests, USA

Energy Technology Data Exchange (ETDEWEB)

Geiser, Linda H., E-mail: lgeiser@fs.fed.u [US Forest Service Pacific Northwest Region Air Resource Management Program, Siuslaw National Forest, PO Box 1148, Corvallis, OR 97339 (United States); Jovan, Sarah E. [US Forest Service Forest Inventory and Analysis Program, Pacific Northwest Research Station, 620 SW Main St, Suite 400, Portland, OR 97205 (United States); Glavich, Doug A. [US Forest Service Pacific Northwest Region Air Resource Management Program, Siuslaw National Forest, PO Box 1148, Corvallis, OR 97339 (United States); Porter, Matthew K. [Laboratory for Atmospheric Research, Washington State University, Pullman, WA 99164 (United States)

2010-07-15

Critical loads (CLs) define maximum atmospheric deposition levels apparently preventative of ecosystem harm. We present first nitrogen CLs for northwestern North America's maritime forests. Using multiple linear regression, we related epiphytic-macrolichen community composition to: 1) wet deposition from the National Atmospheric Deposition Program, 2) wet, dry, and total N deposition from the Communities Multi-Scale Air Quality model, and 3) ambient particulate N from Interagency Monitoring of Protected Visual Environments (IMPROVE). Sensitive species declines of 20-40% were associated with CLs of 1-4 and 3-9 kg N ha{sup -1} y{sup -1} in wet and total deposition. CLs increased with precipitation across the landscape, presumably from dilution or leaching of depositional N. Tight linear correlation between lichen and IMPROVE data suggests a simple screening tool for CL exceedance in US Class I areas. The total N model replicated several US and European lichen CLs and may therefore be helpful in estimating other temperate-forest lichen CLs. - Lichen-based critical loads for N deposition in western Oregon and Washington forests ranged from 3 to 9 kg ha{sup -1} y{sup -1}, increasing with mean annual precipitation.

Optimizing best management practices to control anthropogenic sources of atmospheric phosphorus deposition to inland lakes.

Science.gov (United States)

Weiss, Lee; Thé, Jesse; Winter, Jennifer; Gharabaghi, Bahram

2018-04-18

Excessive phosphorus loading to inland freshwater lakes around the globe has resulted in nuisance plant growth along the waterfronts, degraded habitat for cold water fisheries, and impaired beaches, marinas and waterfront property. The direct atmospheric deposition of phosphorus can be a significant contributing source to inland lakes. The atmospheric deposition monitoring program for Lake Simcoe, Ontario indicates roughly 20% of the annual total phosphorus load (2010-2014 period) is due to direct atmospheric deposition (both wet and dry deposition) on the lake. This novel study presents a first-time application of the Genetic Algorithm (GA) methodology to optimize the application of best management practices (BMPs) related to agriculture and mobile sources to achieve atmospheric phosphorus reduction targets and restore the ecological health of the lake. The novel methodology takes into account the spatial distribution of the emission sources in the airshed, the complex atmospheric long-range transport and deposition processes, cost and efficiency of the popular management practices and social constraints related to the adoption of BMPs. The optimization scenarios suggest that the optimal overall capital investment of approximately $2M, $4M, and $10M annually can achieve roughly 3, 4 and 5 tonnes reduction in atmospheric P load to the lake, respectively. The exponential trend indicates diminishing returns for the investment beyond roughly $3M per year and that focussing much of this investment in the upwind, nearshore area will significantly impact deposition to the lake. The optimization is based on a combination of the lowest-cost, most-beneficial and socially-acceptable management practices that develops a science-informed promotion of implementation/BMP adoption strategy. The geospatial aspect to the optimization (i.e. proximity and location with respect to the lake) will help land managers to encourage the use of these targeted best practices in areas that

Experimental determination of submicron aerosol dry deposition velocity onto rural canopies: influence of aerosol size, of micro meteorological parameters and of the substrate

International Nuclear Information System (INIS)

Damay, P.

2010-04-01

To evaluate the impact of accidental or chronic pollutant releases on ecosystems, we must study the dry deposition of aerosols in rural areas. The lack of experimental data on the dry deposition velocity of particle sizes below 1 μm over rural environments leads to uncertainties regarding models and differences between them, which exceed one order of magnitude. The aim of this study is to develop a method, especially using an Electrical Low Pressure Impactor (Outdoor ELPIDEKATI) to determine aerosol dry deposition velocities (Vd) over rural areas through experimental measurements. This method is based on eddy covariance flux calculation and spectral analysis correction. Dry deposition velocities were obtained for atmospheric aerosols sizing from 7 nm to 2 μm, in the South-West of France on a flat terrain under varied meteorological conditions and varied substrates (maize, grass and earth). Vd was analysed as a function of the particle diameters, and the impact of micro meteorological parameters was studied. (author)

Dry Deposition from Sahara Sources Regions of Western Africa

Directory of Open Access Journals (Sweden)

B. Douaiba

2014-01-01

Full Text Available Sahara dust storms during March 2004 have attracted much attention from the dust-research community due to their intensity, wide coverage, and endurance. In the present work, the dry deposition mechanisms of mineral dust are analysed during an event on the 3 March 2004 over the Northwest African coast. This particular case was chosen based on the strong dry removal that occurred, rendering it ideal for examining the deposition processes. The simulation of synoptic conditions and dry deposition of four dust particles including clay, small silt, large silt, and sand was performed with Eta model, coupled with a desert dust cycle module. The results have been compared with surface data from weather stations in North Africa, data of dry metals from stations located in Gran Canaria, and various satellite images such as European Organization for the Exploitation of Meteorological Satellites and Moderate Resolution Imaging Spectroradiometer for the period in question.

Surface ozone seasonality under global change: Influence from dry deposition and isoprene emissions at northern mid-latitudes

Science.gov (United States)

Clifton, O.; Paulot, F.; Fiore, A. M.; Horowitz, L. W.; Malyshev, S.; Shevliakova, E.; Correa, G. J. P.; Lin, M.

2017-12-01

Identifying the contributions of nonlinear chemistry and transport to observed surface ozone seasonal cycles over land using global models relies on an accurate representation of ozone uptake by vegetation (dry deposition). It is well established that in the absence of ozone precursor emission changes, a warming climate will increase surface ozone in polluted regions, and that a rise in temperature-dependent isoprene emissions would exacerbate this "climate penalty". However, the influence of changes in ozone dry deposition, expected to evolve with climate and land use, is often overlooked in air quality projections. With a new scheme that represents dry deposition within the NOAA GFDL dynamic vegetation land model (LM3) coupled to the NOAA GFDL atmospheric chemistry-climate model (AM3), we simulate the impact of 21st century climate and land use on ozone dry deposition and isoprene emissions. This dry deposition parameterization is a version of the Wesely scheme, but uses parameters explicitly calculated by LM3 that respond to climate and land use (e.g., stomatal conductance, canopy interception of water, leaf area index). The parameterization includes a nonstomatal deposition dependence on humidity. We evaluate climatological present-day seasonal cycles of ozone deposition velocities and abundances with those observed at northern mid-latitude sites. With a set of 2010s and 2090s decadal simulations under a high climate warming scenario (RCP8.5) and a sensitivity simulation with well-mixed greenhouse gases following RCP8.5 but air pollutants held at 2010 levels (RCP8.5_WMGG), we examine changes in surface ozone seasonal cycles. We build on our previous findings, which indicate that strong reductions in anthropogenic NOx emissions under RCP8.5 cause the surface ozone seasonal cycle over the NE USA to reverse, shifting from a summer peak at present to a winter peak by 2100. Under RCP8.5_WMGG, we parse the separate effects of climate and land use on ozone dry

Dry deposition of reactive nitrogen to European ecosystems: a comparison of inferential models across the NitroEurope network

Directory of Open Access Journals (Sweden)

C. R. Flechard

2011-03-01

Full Text Available Inferential models have long been used to determine pollutant dry deposition to ecosystems from measurements of air concentrations and as part of national and regional atmospheric chemistry and transport models, and yet models still suffer very large uncertainties. An inferential network of 55 sites throughout Europe for atmospheric reactive nitrogen (N_r was established in 2007, providing ambient concentrations of gaseous NH₃, NO₂, HNO₃ and HONO and aerosol NH₄⁺ and NO₃⁻ as part of the NitroEurope Integrated Project.

Network results providing modelled inorganic N_r dry deposition to the 55 monitoring sites are presented, using four existing dry deposition routines, revealing inter-model differences and providing ensemble average deposition estimates. Dry deposition is generally largest over forests in regions with large ambient NH₃ concentrations, exceeding 30–40 kg N ha⁻¹ yr⁻¹ over parts of the Netherlands and Belgium, while some remote forests in Scandinavia receive less than 2 kg N ha⁻¹ yr⁻¹. Turbulent N_r deposition to short vegetation ecosystems is generally smaller than to forests due to reduced turbulent exchange, but also because NH₃ inputs to fertilised, agricultural systems are limited by the presence of a substantial NH₃ source in the vegetation, leading to periods of emission as well as deposition.

Differences between models reach a factor 2–3 and are often greater than differences between monitoring sites. For soluble N_r gases such as NH₃ and HNO₃, the non-stomatal pathways are responsible for most of the annual uptake over many surfaces, especially the non-agricultural land uses, but parameterisations of the sink strength vary considerably among models. For aerosol NH₄

Lichens as biomonitors of atmospheric ammonium/ammonia deposition in Portugal

International Nuclear Information System (INIS)

Capelao, A.L.; Maguas, C.; Branquinho, C.; Cruz, C.; Martins-Loucao, M.A.

2000-01-01

The aim of the present work was to evaluate the potentiality of lichens as biomonitors of NH 4 + /NH 3 (ammonium/ammonia) and NO 3 - (nitrate) atmospheric deposition. For that, we used as a field station a rice plantation which is submitted, once a year, to air spraying fertilization with a mixture of nitrogen sources. Samples of an epiphytic lichen, Ramalina fastigiata, were collected from an ash-tree bordering the rice-plantation by the Sorraia River Valley (Central Portugal). The study started one month before fertilization and sampling was carried out for five months. The concentration of ammonium in the lichen was highly and significantly correlated with the number of days without precipitation before sampling, and had an inverse correlation with fluorescence values. Under these conditions, the amount of NH 4 + found in the lichen appears to reflect ammonium/ammonia dry deposition. (author)

Steam atmosphere drying concepts using steam exhaust recompression

Energy Technology Data Exchange (ETDEWEB)

DiBella, F.A. (TECOGEN, Inc., Waltham, MA (United States))

1992-08-01

In the US industrial drying accounts for approximately 1.5 quads of energy use per year. Annual industrial dryer expenditures are estimated to be in the $500 million range. Industrial drying is a significant energy and monetary expense. For the thermal drying processes in which water is removed via evaporation from the feedstock, attempts have been made to reduce the consumption of energy using exhaust waste heat recovery techniques, improved dryer designs, or even the deployment of advanced mechanical dewatering techniques. Despite these efforts, it is obvious that a large amount of thermal energy is often still lost if the latent heat of evaporation from the evaporated water cannot be recovered and/or in some way be utilized as direct heat input into the dryer. Tecogen Inc. is conducting research and development on an industrial drying concept. That utilizes a directly or indirectly superheated steam cycle atmosphere with exhaust steam recompression to recover the latent heat in the exhaust that would otherwise be lost. This approach has the potential to save 55 percent of the energy required by a conventional air dryer. Other advantages to the industrial dryer user include: A 35-percent reduction in the yearly cost per kg[sub evap] to dry wet feedstock, Reduced airborne emissions, Reduced dry dust fire/explosion risks, Hot product not exposed to oxygen thus, the product quality is enhanced, Constant rate drying in steam atmosphere, Reduced dryer size and cost, Reduced dryer heat losses due to lower dryer inlet temperatures. Tecogen has projected that the steam atmosphere drying system is most suitable as a replacement technology for state-of-the-art spray, flash, and fluidized bed drying systems. Such systems are utilized in the food and kindred products; rubber products; chemical and allied products; stone, clay, and glass; textiles; and pulp and paper industrial sectors.

Steam atmosphere drying concepts using steam exhaust recompression

Energy Technology Data Exchange (ETDEWEB)

DiBella, F.A. [TECOGEN, Inc., Waltham, MA (United States)

1992-08-01

In the US industrial drying accounts for approximately 1.5 quads of energy use per year. Annual industrial dryer expenditures are estimated to be in the $500 million range. Industrial drying is a significant energy and monetary expense. For the thermal drying processes in which water is removed via evaporation from the feedstock, attempts have been made to reduce the consumption of energy using exhaust waste heat recovery techniques, improved dryer designs, or even the deployment of advanced mechanical dewatering techniques. Despite these efforts, it is obvious that a large amount of thermal energy is often still lost if the latent heat of evaporation from the evaporated water cannot be recovered and/or in some way be utilized as direct heat input into the dryer. Tecogen Inc. is conducting research and development on an industrial drying concept. That utilizes a directly or indirectly superheated steam cycle atmosphere with exhaust steam recompression to recover the latent heat in the exhaust that would otherwise be lost. This approach has the potential to save 55 percent of the energy required by a conventional air dryer. Other advantages to the industrial dryer user include: A 35-percent reduction in the yearly cost per kg{sub evap} to dry wet feedstock, Reduced airborne emissions, Reduced dry dust fire/explosion risks, Hot product not exposed to oxygen thus, the product quality is enhanced, Constant rate drying in steam atmosphere, Reduced dryer size and cost, Reduced dryer heat losses due to lower dryer inlet temperatures. Tecogen has projected that the steam atmosphere drying system is most suitable as a replacement technology for state-of-the-art spray, flash, and fluidized bed drying systems. Such systems are utilized in the food and kindred products; rubber products; chemical and allied products; stone, clay, and glass; textiles; and pulp and paper industrial sectors.

MEAD Marine Effects of Atmospheric Deposition

Science.gov (United States)

Jickells, T.; Spokes, L.

2003-04-01

The coastal seas are one of the most valuable resources on the planet but they are threatened by human activity. We rely on the coastal area for mineral resources, waste disposal, fisheries and recreation. In Europe, high population densities and high levels of industrial activity mean that the pressures arising from these activities are particularly acute. One of the main problems concerning coastal seas is the rapid increase in the amounts of nitrogen-based pollutants entering the water. They come from many sources, the most important ones being traffic, industry and agriculture. These pollutants can be used by algae as nutrients. The increasing concentrations of these nutrients have led to excessive growth of algae, some of which are harmful. When algae die and decay, oxygen in the water is used up and the resulting lower levels of oxygen may lead to fish kills. Human activity has probably doubled the amount of chemically and biologically reactive nitrogen present globally. In Europe the increases have been greater than this, leading to real concern over the health of coastal waters. Rivers have, until recently, been thought to be the most important source of reactive nitrogen to the coastal seas but we now know that inputs from the atmosphere are large and can equal, or exceed, those from the rivers. Our initial hypothesis was that atmospheric inputs are important and potentially different in their effect on coastal ecosystems to riverine inputs and hence require different management strategies. However, we had almost no information on the direct effects of atmospheric deposition on marine ecosystems, though clearly such a large external nitrogen input should lead to enhanced phytoplankton growth The aim of this European Union funded MEAD project has been to determine how inputs of nitrogen from the atmosphere affect the chemistry and biology of coastal waters. To try to answer this, we have conducted field experiments in the Kattegat, an area where we know

Size distribution of atmospheric Pb and 210Pb in rural New Jersey: implications for wet and dry deposition

International Nuclear Information System (INIS)

Knuth, R.H.; Knutson, E.O.; Feely, H.W.; Volchok, H.L.

1983-01-01

High volume cascade impactor samples taken during spring, 1980, at the Chester sampling station in northern New Jersey showed a small but persistent difference in the size distributions of Pb and 210 Pb. On the average, 69% of Pb was below 0.58 μm and 12% was above 3.45 μm. For 210 Pb, the corresponding figures were 71% and 2.8%. These 210 Pb data indicate larger particles than found in Colorado, but smaller than those found over the Mediterranean Sea. The average air concentrations for the two species were 111 ng/m 3 (Pb) and 10.9 fCi/m 3 ( 210 Pb), in good agreement with other reported results for rural northeast areas. Experimental results imply a factor of three difference in dry deposition velocity between the two species, providing a qualitative explanation of a previously observed difference in wet/dry deposition of the two species. 19 references, 1 figure, 6 tables

Simulated dry deposition of nitric acid near forest edges

NARCIS (Netherlands)

DeJong, JJM; Klaassen, W; Jong, J.J.M. de

1997-01-01

Dry deposition is simulated to understand and generalize observations of enhanced deposition of air pollution near forest edges. Nitric acid is taken as an example as its deposition velocity is often assumed to be determined by turbulent transport only. The simulations are based on the

DRY DEPOSITION OF POLLUTANTS TO FORESTS

Science.gov (United States)

We report on the results of an extensive field campaign to measure dry deposition of ozone and sulfur dioxide to a sample of forest types in the United States. Measurements were made for full growing seasons over a deciduous forest in Pennsylvania and a mixed deciduous-conifer...

Deposition and retention of air pollutants on vegetation and other atmospheric interfaces

International Nuclear Information System (INIS)

Jonas, R.

1984-09-01

The question of the deposition of aerosols and gases are applied to biological and ecological problems concerning the filtering aspect of atmospheric interfaces, especially vegetation, with respect to air pollution, and also the resulting pollutant effect. In order to determine the deposition of aerosols, numerous field experiments were carried out. The deposition of gases was treated on the basis of current literature data. The experiments indicate that the deposition of aerosols on grass largely depends on aerosol diameter, dry weight per unit area and the wind velocity or turbulence of the air layer near the ground. Of the interfaces studied, namely soil without vegetation, water, filter paper, smooth and structured metals, grass, clover and trees, the latter had the greatest dust collecting capability. It is recommended that in the afforestation of areas in the close proximity of industrial regions the common beech, silver birch and Japanese larch should be taken into particular consideration due to their great deposition effectiveness with respect to dusts and their comparatively high resistance to pollutant gases. Silver birch and moreover red horse chestnut should be considered for filtering the air in urban regions because of the high aerosol deposition. (orig./HP) [de

Patterned deposition by atmospheric pressure plasma-enhanced spatial atomic layer deposition

NARCIS (Netherlands)

Poodt, P.; Kniknie, B.J.; Branca, A.; Winands, G.J.J.; Roozeboom, F.

2011-01-01

An atmospheric pressure plasma enhanced atomic layer deposition reactor has been developed, to deposit Al2O3 films from trimethyl aluminum and an He/O2 plasma. This technique can be used for 2D patterned deposition in a single in-line process by making use of switched localized plasma sources. It

Long-term effects of changing atmospheric pollution on throughfall, bulk deposition and streamwaters in a Mediterranean forest.

Science.gov (United States)

Aguillaume, Laura; Rodrigo, Anselm; Avila, Anna

2016-02-15

The abatement programs implanted in Europe to reduce SO2, NO2 and NH3 emissions are here evaluated by analyzing the relationships between emissions in Spain and neighboring countries and atmospheric deposition in a Mediterranean forest in the Montseny mountains (NE Spain) for the last 3decades. A canopy budget model was applied to throughfall data measured during a period of high emissions (1995-1996) and a period of lower emissions (2011-2013) to estimate the changes in dry deposition over this time span. Emissions of SO2 in Spain strongly decreased (77%) and that was reflected in reductions for nssSO4(2-) in precipitation (65% for concentrations and 62% for SO4(2)-S deposition). A lower decline was found for dry deposition (29%). Spanish NO2 emissions increased from 1980 to 1991, remained constant until 2005, and decreased thereafter, a pattern that was paralleled by NO3(-) concentrations in bulk precipitation at Montseny. This pattern seems to be related to a higher share of renewable energies in electricity generation in Spain in recent years. However, dry deposition increased markedly between 1995 and 2012, from 1.3 to 6.7 kg ha(-1) year(-)(1). Differences in meteorology between periods may have had a role, since the recent period was drier thus probably favoring dry deposition. Spanish NH3 emissions increased by 13% between 1980 and 2012 in Spain but NH4(+) concentrations in precipitation and NH4(+)-N deposition showed a decreasing trend (15% reduction) at Montseny, probably linked to the reduction ammonium sulfate and nitrate aerosols to be scavenged by rainfall. NH4(+)-N dry deposition was similar between the compared periods. The N load at Montseny (15-17 kg ha(-1)y ear(-1)) was within the critical load range proposed for Mediterranean sclerophyllous forests (15-17.5 kg ha(-1) year(-1)). The onset of N saturation is suggested by the observed increasing N export in streamwaters. Copyright © 2015 Elsevier B.V. All rights reserved.

Dry deposition of sulfate to Quercus rubra and Liriodendron tulipifera foliage

International Nuclear Information System (INIS)

Vandenberg, J.J.

1987-01-01

Estimates were made of the rate of dry deposition to red oak (Quercus rubra) and tulip poplar (Liriodendron tulipifera) foliage. In the laboratory, radioactive ammonium sulfate aerosols were generated in an exposure chamber. These aerosols were dry deposited onto leaves that were sequentially washed to examine the efficacy of washing procedures in removal of surface deposits. Over 90% of dry deposited sulfate was removed after a 30 second wash duration. Laboratory procedures also estimated the magnitude of foliar sulfur that leached into leaf wash solutions. The majority of laboratory leaves demonstrated no leaching of sulfur from the internal pool. However, some leaves showed significant sulfur leaching. It was concluded that leaching of internal sulfur was highly leaf specific. This indicated that each leaf used in field experiments needed to be individually examined for leaching

Image analysis of epicuticular damage to foliage caused by dry deposition of the air pollutant nitric acid.

Science.gov (United States)

Padgett, Pamela E; Parry, Sally D; Bytnerowicz, Andrzej; Heath, Robert L

2009-01-01

Nitric acid vapor is produced by the same photochemical processes that produce ozone. In the laboratory, concentrated nitric acid is a strong acid and a powerful oxidant. In the environment, where the concentrations are much lower, it is an innocuous source of plant nitrogen. As an air pollutant, which mode of action does dry deposition of nitric acid follow? We investigated the effects of dry deposition of nitric acid on the foliage of four tree species native to the western United States. A novel controlled environment, fumigation system enabled a four-week exposure at concentrations consistent with ambient diurnal patterns. Scanning electron microscopy and automated image analysis revealed changes in the epicuticular wax layer during fumigation. Exposure to nitric acid resulted in a reproducible suite of damage symptoms that increased with increasing dose. Each tree species tested exhibited a unique set of damage features, including cracks, lesions, and conformation changes to epicuticular crystallite structures. Dry deposition of atmospheric nitric acid caused substantial perturbation to the epicuticular surface of all four tree species investigated, consistent with the chemical oxidation of epicuticular waxes. Automated image analysis eliminated many biases that can trouble microscopy studies. Trade names and commercial enterprises or products are mentioned solely for information. No endorsements by the U.S. Department of Agriculture are implied.

Development of the aerosol generation system for simulating the dry deposition behavior of radioaerosol emitted by the accident of FDNPP

Science.gov (United States)

Zhang, Z.

2015-12-01

A large amount of radioactivity was discharged by the accident of FDNPP. The long half-life radionuclide, 137Cs was transported through the atmosphere mainly as the aerosol form and deposited to the forests in Fukushima prefecture. After the dry deposition of the 137Cs, the foliar uptake process would occur. To evaluate environmental transfer of radionuclides, the dry deposition and following foliar uptake is very important. There are some pioneering studies for radionuclide foliar uptake with attaching the solution containing stable target element on the leaf, however, cesium oxide aerosols were used for these deposition study [1]. In the FDNPP case, 137Cs was transported in sulfate aerosol form [2], so the oxide aerosol behaviors could not represent the actual deposition behavior in this accident. For evaluation of whole behavior of 137Cs in vegetation system, fundamental data for deposition and uptake process of sulfate aerosol was desired. In this study, we developed aerosol generation system for simulating the dry deposition and the foliar uptake behaviors of aerosol in the different chemical constitutions. In this system, the method of aerosol generation based on the spray drying. Solution contained 137Cs was send to a nozzle by a syringe pump and spraying with a high speed air flow. The sprayed mist was generated in a chamber in the relatively high temperature. The solution in the mist was dried quickly, and micro size solid aerosols consisting 137Cs were generated. The aerosols were suctioned by an ejector and transported inside a tube by the dry air flow, then were directly blown onto the leaves. The experimental condition, such as the size of chamber, chamber temperature, solution flow rate, air flow rate and so on, were optimized. In the deposition experiment, the aerosols on leaves were observed by a SEM/EDX system and the deposition amount was evaluated by measuring the stable Cs remaining on leaf. In the presentation, we will discuss the detail

NDE to Manage Atmospheric SCC in Canisters for Dry Storage of Spent Fuel: An Assessment

Energy Technology Data Exchange (ETDEWEB)

Meyer, Ryan M. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Pardini, Allan F. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Cuta, Judith M. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Adkins, Harold E. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Casella, Andrew M. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Qiao, Hong [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Larche, Michael R. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Diaz, Aaron A. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Doctor, Steven R. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

2013-09-01

This report documents efforts to assess representative horizontal (Transuclear NUHOMS®) and vertical (Holtec HI-STORM) storage systems for the implementation of non-destructive examination (NDE) methods or techniques to manage atmospheric stress corrosion cracking (SCC) in canisters for dry storage of used nuclear fuel. The assessment is conducted by assessing accessibility and deployment, environmental compatibility, and applicability of NDE methods. A recommendation of this assessment is to focus on bulk ultrasonic and eddy current techniques for direct canister monitoring of atmospheric SCC. This assessment also highlights canister regions that may be most vulnerable to atmospheric SCC to guide the use of bulk ultrasonic and eddy current examinations. An assessment of accessibility also identifies canister regions that are easiest and more difficult to access through the ventilation paths of the concrete shielding modules. A conceivable sampling strategy for canister inspections is to sample only the easiest to access portions of vulnerable regions. There are aspects to performing an NDE inspection of dry canister storage system (DCSS) canisters for atmospheric SCC that have not been addressed in previous performance studies. These aspects provide the basis for recommendations of future efforts to determine the capability and performance of eddy current and bulk ultrasonic examinations for atmospheric SCC in DCSS canisters. Finally, other important areas of investigation are identified including the development of instrumented surveillance specimens to identify when conditions are conducive for atmospheric SCC, characterization of atmospheric SCC morphology, and an assessment of air flow patterns over canister surfaces and their influence on chloride deposition.

Atmospheric deposition of nitrogen at five subtropical forested sites in South China

International Nuclear Information System (INIS)

Chen, Xi Yun; Mulder, Jan

2007-01-01

Elevated concentrations of reactive nitrogen (N) in precipitation have been reported for many cities in China. Due to increased use of fossil fuels and expansion in agriculture, further increases in deposition of ammonia (NH x ) and reactive N oxides (NO y ) are predicted. Increased deposition of reactive N is likely to affect N dynamics and N runoff in forest ecosystems. Yet, in China little work has been done to quantify the levels of atmospheric N deposition in such systems. Here, we assess the deposition of inorganic N (ammonium, NH 4 + and nitrate, NO 3 - ) for five subtropical forest ecosystems in remote and urban areas of South China. Annual volume-weighted concentrations in bulk precipitation range from 0.18 to 1.55 mg NH 4 + -N L - 1 and from 0.12 to 0.74 mg NO 3 - -N L - 1 . These values are large and several times greater than those reported for remote sites of the world. The fluxes of total inorganic N (TIN) in wet-only deposition range from 0.8 to 2.3 g N m - 2 yr - 1 , with NH 4 + -N contributing 54% to 77%. Both the tree canopy and the ground vegetation layer are important in determining the net N flux reaching the forest floor, but the net effect varies from site to site. At TieShanPing (TSP), close to Chongqing city, and at CaiJiaTang (CJT), near Shaoshan (Hunan province), the canopy represents a net source of N, probably due to dry deposition. At the other three sites (LiuChongGuan (LCG), LeiGongShan (LGS), both in Guizhou province, and LiuXiHe (LXH) in Guangdong), a net loss of reactive N from precipitation water occurs in the canopy, probably due to uptake processes. The total annual atmospheric TIN load is estimated to range from at least 0.8 g N m - 2 yr - 1 to 4.0 g N m - 2 yr - 1 , with a considerable contribution from dry deposition. Concentrations and fluxes of inorganic N in tree canopy throughfall are greater than those in North America. Also the contribution of NH 4 + -N to TIN fluxes in throughfall (40% to 70%) is greater than in North

Atmospheric deposition of organochlorine contaminants to Galveston Bay, Texas

Science.gov (United States)

Park, June-Soo; Wade, Terry L.; Sweet, Stephen

Atmospheric monitoring of PCBs and chlorinated pesticides (e.g., HCHs, chlordanes, and DDTs) in Galveston Bay was conducted at Seabrook, Texas. Air and wet deposition samples were collected from 2 February 1995 and continued through 6 August 1996. Vapor total PCB ( tPCB) concentrations in air ranged from 0.21 to 4.78 ng m -3 with a dominance of tri-chlorinated PCBs. Dissolved tPCBs in rain ranged from 0.08 to 3.34 ng l -1, with tetra-chlorinated PCBs predominating. The predominant isomers found in air and rain were α- and γ-HCH, α- and γ-chlordanes, 4,4'-DDT, and dieldrin. The concentrations of PCBs and pesticides in the air and rain revealed no clear seasonal trend. Elevated levels of PCBs in the air occurred when temperatures were high and wind came from urban and industrialized areas (S, SW, NW, and W of the site). Concentrations of HCHs were elevated in April, May, and October, perhaps due to local and/or regional applications of γ-HCH (lindane). Other pesticides showed no notable temporal variation. When winds originated from the Gulf of Mexico (southeasterly), lower concentrations of organochlorines were detected in the air. The direct deposition rate (wet+dry) of PCBs to Galveston Bay (6.40 μg m -2 yr -1) was significantly higher than that of pesticides by a factor of 5-10. The net flux from gas exchange estimated for PCBs was from Galveston Bay water to the atmosphere (78 μg m -2 yr -1). Gas exchange of PCBs from bay water to the atmosphere was the dominant flux.

High 210Po atmospheric deposition flux in the subtropical coastal area of Japan

International Nuclear Information System (INIS)

Tateda, Yutaka; Iwao, Kenji

2008-01-01

Bulk atmospheric deposition fluxes of 210 Po and 210 Pb were measured at three coastal regions of Japan, the Pacific Ocean coastal area of the Japanese mainland (Odawa Bay), the Chinese continental side of Japanese coastal area (Tsuyazaki), and an isolated island near Okinawa (Akajima). Wet and dry fallout collectors were continuously deployed from September 1997 through August 1998 for periods of 3 to 31 days depending on the frequency of precipitation events. Annual 210 Pb deposition fluxes at Odawa Bay (35 o N 139 o E), Tsuyazaki (33 o N 130 o E) and Akajima (26 o N 127 o E) were 73.3 ± 8.0, 197 ± 35 and 78.5 ± 8.0 Bq m -2 y -1 , respectively. Higher 210 Pb deposition was observed at the Chinese continental side of Japanese coast than at the Pacific Ocean coastal site. The high 210 Pb atmospheric flux at the Chinese continental side coast was thought to be attributable to 222 Rn-rich air-mass transport from the Chinese continent during the winter monsoon. In contrast, the annual 210 Po deposition fluxes at the three study sites were 13.0 ± 2.3 (Odawa Bay), 21.9 ± 4.4 (Tsuyazaki) and 58.4 ± 7.7 (Akajima) Bq m -2 y -1 , respectively, indicating unusual high 210 Po deposition at Akajima during winter. Anomalous unsupported 210 Po input was observed during summer 1997, suggesting unknown source of 210 Po at this area

Total Sulfur Deposition (wet+dry) from the Atmosphere

Data.gov (United States)

U.S. Environmental Protection Agency — Sulfur Dioxide (SO2) is emitted primarily as a by-product of coal combustion from power plants. Sulfur Dioxide reacts in the atmosphere to form other chemical such...

Evaluation and intercomparison of five major dry deposition algorithms in North America

Science.gov (United States)

Dry deposition of various pollutants needs to be quantified in air quality monitoring networks as well as in chemical transport models. The inferential method is the most commonly used approach in which the dry deposition velocity (Vd) is empirically parameterized as a function o...

Seasonal Patterns of Dry Deposition at a High-Elevation Site in the Colorado Rocky Mountains

Science.gov (United States)

Oldani, Kaley M.; Mladenov, Natalie; Williams, Mark W.; Campbell, Cari M.; Lipson, David A.

2017-10-01

In the Colorado Rocky Mountains, high-elevation barren soils are deficient in carbon (C) and phosphorus (P) and enriched in nitrogen (N). The seasonal variability of dry deposition and its contributions to alpine elemental budgets is critical to understanding how dry deposition influences biogeochemical cycling in high-elevation environments. In this 2 year study, we evaluated dry and wet deposition inputs to the Niwot Ridge Long Term Ecological Research (NWT LTER) site in the Colorado Rocky Mountains. The total organic C flux in wet + dry (including soluble and particulate C) deposition was >30 kg C ha-1 yr-1 and represents a substantial input for this C-limited environment. Our side-by-side comparison of dry deposition collectors with and without marble insert indicated that the insert improved retention of dry deposition by 28%. Annual average dry deposition fluxes of water-soluble organic carbon (4.25 kg C ha-1 yr-1) and other water-soluble constituents, including ammonium (0.16 kg NH4+ha-1 yr-1), nitrate (1.99 kg NO3- ha-1 yr-1), phosphate (0.08 kg PO43- ha-1 yr-1), and sulfate (1.20 kg SO42- ha-1 yr-1), were comparable to those in wet deposition, with highest values measured in the summer. Backward trajectory analyses implicate air masses passing through the arid west and Four Corners, USA, as dominant source areas for dry deposition, especially in spring months. Synchronous temporal patterns of deposition observed at the NWT LTER site and a distant Rocky Mountain National Park Clean Air Status and Trends Network site indicate that seasonal dry deposition patterns are regional phenomena with important implications for the larger Rocky Mountain region.

UFOMOD - atmospheric dispersion and deposition

International Nuclear Information System (INIS)

Panitz, H.J.; Matzerath, C.; Paesler-Sauer, J.

1989-10-01

The report gives an introduction into the modelling of atmospheric dispersion and deposition which has been implemented in the new program system UFOMOD for assessing the consequences after nuclear accidents. According to the new structure of UFOMOD, different trajectory models with ranges of validity near to the site and at far distances are applied. Emphasis is laid on the description of the segmented plume model MUSEMET and its affilated submodels, being the removal of activity from the cloud by dry and wet deposition, and special effects like plume rise and the behaviour of plumes released into building wakes. In addition, the evaluation of γ-dose correction factors to take account of the finite extent of the radioactive plume in the near range (up to about 20 km) are described. Only brief introductions are given into the principles of the other models available: the puff model RIMPUFF, the long-range puff model MESOS, and the special straight-line Gaussian model ISOLA which are used if low-level long-duration releases are considered. To define starting times of weather sequences and the probabilities of occurrence of these sequences, it is convenient to perform stratified sampling. Therefore, the preprocessing program package METSAM has been developed to perform for generic ACAs a random sampling of weather sequences out off a population of classified weather conditions. The sampling procedure and a detailed input/output (I/O) description is presented and an additional appendix, respectively. A general overview on the I/O structure of MUSEMET as well as a brief user guide to run the KfK version of the MESOS code are also given in the appendix. (orig.) [de

Decreased atmospheric sulfur deposition across the southeastern U.S.: When will watersheds release stored sulfate?

Science.gov (United States)

Rice, Karen C.; Scanlon, Todd M.; Lynch, Jason A.; Cosby, Bernard J.

2014-01-01

Emissions of sulfur dioxide (SO2) to the atmosphere lead to atmospheric deposition of sulfate (SO42-), which is the dominant strong acid anion causing acidification of surface waters and soils in the eastern United States (U.S.). Since passage of the Clean Air Act and its Amendments, atmospheric deposition of SO2 in this region has declined by over 80%, but few corresponding decreases in stream-water SO42- concentrations have been observed in unglaciated watersheds. We calculated SO42- mass balances for 27 forested, unglaciated watersheds from Pennsylvania to Georgia, by using total atmospheric deposition (wet plus dry) as input. Many of these watersheds still retain SO42-, unlike their counterparts in the northeastern U.S. and southern Canada. Our analysis showed that many of these watersheds should convert from retaining to releasing SO42- over the next two decades. The specific years when the watersheds crossover from retaining to releasing SO42- correspond to a general geographical pattern of later net watershed release from north to south. The single most important variable that explained the crossover year was the runoff ratio, defined as the ratio of annual mean stream discharge to precipitation. Percent clay content and mean soil depth were secondary factors in predicting crossover year. The conversion of watersheds from net SO42- retention to release anticipates more widespread reductions in stream-water SO42- concentrations in this region.

An Artificial Turf-Based Surrogate Surface Collector for the Direct Measurement of Atmospheric Mercury Dry Deposition

Directory of Open Access Journals (Sweden)

Naima L. Hall

2017-02-01

Full Text Available This paper describes the development of a new artificial turf surrogate surface (ATSS sampler for use in the measurement of mercury (Hg dry deposition. In contrast to many existing surrogate surface designs, the ATSS utilizes a three-dimensional deposition surface that may more closely mimic the physical structure of many natural surfaces than traditional flat surrogate surface designs (water, filter, greased Mylar film. The ATSS has been designed to overcome several complicating factors that can impact the integrity of samples with other direct measurement approaches by providing a passive system which can be deployed for both short and extended periods of time (days to weeks, and is not contaminated by precipitation and/or invalidated by strong winds. Performance characteristics including collocated precision, in-field procedural and laboratory blanks were evaluated. The results of these performance evaluations included a mean collocated precision of 9%, low blanks (0.8 ng, high extraction efficiency (97%–103%, and a quantitative matrix spike recovery (100%.

Atmospheric deposition and air-sea gas exchange fluxes of DDT and HCH in the Yangtze River Estuary, East China Sea

Science.gov (United States)

Li, Zhongxia; Lin, Tian; Li, Yuanyuan; Jiang, Yuqing; Guo, Zhigang

2017-07-01

The Yangtze River Estuary (YRE) is strongly influenced by the Yangtze River and lies on the pathway of the East Asian Monsoon. This study examined atmospheric deposition and air-sea gas exchange fluxes of dichlorodiphenyltrichloroethane (DDT) and hexachlorocyclohexane (HCH) to determine whether the YRE is a sink or source of selected pesticides at the air-water interface under the influences of river input and atmospheric transport. The air-sea gas exchange of DDT was characterized by net volatilization with a marked difference in its fluxes between summer (140 ng/m2/d) and the other three seasons (12 ng/m2/d), possibly due to the high surface seawater temperatures and larger riverine input in summer. However, there was no obvious seasonal variation in the atmospheric HCH deposition, and the air-sea gas exchange reached equilibrium because of low HCH levels in the air and seawater after the long-term banning of HCH and the degradation. The gas exchange flux of HCH was comparable to the dry and wet deposition fluxes at the air-water interface. This suggests that the influences from the Yangtze River input and East Asian continental outflow on the fate of HCH in the YRE were limited. The gas exchange flux of DDT was about fivefold higher than the total dry and wet deposition fluxes. DDT residues in agricultural soil transported by enhanced riverine runoff were responsible for sustaining such a high net volatilization in summer. Moreover, our results indicated that there were fresh sources of DDT from the local environment to sustain net volatilization throughout the year.

Global Atmosphere Watch Workshop on Measurement-Model ...

Science.gov (United States)

The World Meteorological Organization’s (WMO) Global Atmosphere Watch (GAW) Programme coordinates high-quality observations of atmospheric composition from global to local scales with the aim to drive high-quality and high-impact science while co-producing a new generation of products and services. In line with this vision, GAW’s Scientific Advisory Group for Total Atmospheric Deposition (SAG-TAD) has a mandate to produce global maps of wet, dry and total atmospheric deposition for important atmospheric chemicals to enable research into biogeochemical cycles and assessments of ecosystem and human health effects. The most suitable scientific approach for this activity is the emerging technique of measurement-model fusion for total atmospheric deposition. This technique requires global-scale measurements of atmospheric trace gases, particles, precipitation composition and precipitation depth, as well as predictions of the same from global/regional chemical transport models. The fusion of measurement and model results requires data assimilation and mapping techniques. The objective of the GAW Workshop on Measurement-Model Fusion for Global Total Atmospheric Deposition (MMF-GTAD), an initiative of the SAG-TAD, was to review the state-of-the-science and explore the feasibility and methodology of producing, on a routine retrospective basis, global maps of atmospheric gas and aerosol concentrations as well as wet, dry and total deposition via measurement-model

Magma ascent, fragmentation and depositional characteristics of "dry" maar volcanoes: Similarities with vent-facies kimberlite deposits

Science.gov (United States)

Berghuijs, Jaap F.; Mattsson, Hannes B.

2013-02-01

Several maar craters within the Lake Natron-Engaruka monogenetic volcanic field (LNE-MVF) of northern Tanzania show compelling evidence for magmatic fragmentation and dry deposition. This is in contradiction of the common belief that most maars are formed through the explosive interaction between ascending magma and ground- or surface water. We here present a detailed study on the eruptive and depositional characteristics of the Loolmurwak and Eledoi maar volcanoes, two of the largest craters in the LNE-MVF, focusing on high-resolution stratigraphy, sedimentology, grain size distribution, pyroclast textures and morphologies, bulk geochemistry and mineral chemistry. At both maars, ejected material has been emplaced by a combination of pyroclastic surges and fallout. Indicators of phreatomagmatic fragmentation and wet deposition, such as impact sags, accretionary lapilli, vesiculated tuffs and plastering against obstacles, are absent in the deposits. Juvenile material predominantly occurs as fluidal-shaped vesicular melt droplets and contains no glass shards produced by the breakage of bubble walls. The Eledoi deposits comprise a large amount of inversely graded beds and lenses, which result from grain flow in a dry depositional environment. Preferential deposition of fine material toward the northern side of its crater can be related to effective wind winnowing in a dry eruption plume. This large variety of observations testifies to the dominance of magmatic fragmentation as well as dry deposition at the Loolmurwak and Eledoi maars, which is in line with what has been found for other structures in the LNE-MVF but contrasts with current ideas on maar formation. We infer that a volatile-rich, olivine melilitic magma was formed by small amounts of partial melting at upper mantle depths. With minimum average ascent rates of 5.3 m s- 1 for Loolmurwak and 26.2 m s- 1 for Eledoi, this magma rapidly moved toward the surface and exsolved a substantial amount of volatiles

Atmospheric deposition of beryllium in Central Europe: Comparison of soluble and insoluble fractions in rime and snow across a pollution gradient

International Nuclear Information System (INIS)

Bohdalkova, Leona; Novak, Martin; Voldrichova, Petra; Prechova, Eva; Veselovsky, Frantisek; Erbanova, Lucie; Krachler, Michael; Komarek, Arnost; Mikova, Jitka

2012-01-01

Little is known about atmospheric input of beryllium (Be) into ecosystems, despite its highly toxic behavior. For three consecutive winters (2009–2011), we measured Be concentrations in horizontal deposition (rime) and vertical deposition (snow) at 10 remote mountain-top locations in the Czech Republic, Central Europe. Beryllium was determined both in filtered waters, and in HF digests of insoluble particles. Across the sites, soluble Be concentrations in rime were 7 times higher, compared to snow (6.1 vs. 0.9 ng·L −1 ). Rime scavenged the pollution-rich lower segments of clouds. The lowest Be concentrations were detected in the soluble fraction of snow. Across the sites, 34% of total Be deposition occurred in the form of soluble (bioavailable) Be, the rest were insoluble particles. Beryllium fluxes decreased in the order: vertical dry deposition insoluble > vertical dry deposition soluble > horizontal deposition soluble > vertical wet deposition insoluble > vertical wet deposition soluble > horizontal deposition insoluble. The average contributions of these Be forms to total deposition were 56, 21, 8, 7, 5 and 3%, respectively. Sites in the northeast were more Be-polluted than the rest of the country with sources of pollution in industrial Silesia. -- Highlights: ► We measured Be concentrations in rime and snow in the Czech Republic. ► Soluble Be concentrations in rime were 7 times higher than in snow. ► 34% of total Be deposition occurred in the form of soluble (bioavailable) Be. ► Dry-deposited fluxes dominated Be inputs. ► Soluble Be concentrations only rarely exceeded 30 ng·L −1 .

Laboratory study of SO2 dry deposition on limestone and marble: Effects of humidity and surface variables

Science.gov (United States)

Spiker, E. C.; Hosker, R.P.; Weintraub, V.C.; Sherwood, S.I.

1995-01-01

The dry deposition of gaseous air pollutants on stone and other materials is influenced by atmospheric processes and the chemical characteristics of the deposited gas species and of the specific receptor material. Previous studies have shown that relative humidity, surface moisture, and acid buffering capability of the receptor surface are very important factors. To better quantify this behavior, a special recirculating wind tunnel/environmental chamber was constructed, in which wind speed, turbulence, air temperature, relative humidity, and concentrations of several pollutants (SO2, O3, nitrogen oxides) can be held constant. An airfoil sample holder holds up to eight stone samples (3.8 cm in diameter and 1 cm thick) in nearly identical exposure conditions. SO2 deposition on limestone was found to increase exponentially with increasing relative humidity (RH). Marble behaves similarly, but with a much lower deposition rate. Trends indicate there is little deposition below 20% RH on clean limestone and below 60% RH on clean marble. This large difference is due to the limestone's greater porosity, surface roughness, and effective surface area. These results indicate surface variables generally limit SO2 deposition below about 70% RH on limestone and below at least 95% RH on marble. Aerodynamic variables generally limit deposition at higher relative humidity or when the surface is wet.The dry deposition of gaseous air pollutants on stone and other materials is influenced by atmospheric processes and the chemical characteristics of the deposited gas species and of the specific receptor material. Previous studies have shown that relative humidity, surface moisture, and acid buffering capability of the receptor surface are very important factors. To better quantify this behavior, a special recirculating wind tunnel/environmental chamber was constructed, in which wind speed, turbulence, air temperature, relative humidity, and concentrations of several pollutants (SO2, O3

Tracing the Sources of Atmospheric Phosphorus Deposition to a Tropical Rain Forest in Panama Using Stable Oxygen Isotopes.

Science.gov (United States)

Gross, A; Turner, B L; Goren, T; Berry, A; Angert, A

2016-02-02

Atmospheric dust deposition can be a significant source of phosphorus (P) in some tropical forests, so information on the origins and solubility of atmospheric P is needed to understand and predict patterns of forest productivity under future climate scenarios. We characterized atmospheric dust P across a seasonal cycle in a tropical lowland rain forest on Barro Colorado Nature Monument (BCNM), Republic of Panama. We traced P sources by combining remote sensing imagery with the first measurements of stable oxygen isotopes in soluble inorganic phosphate (δ(18)OP) in dust. In addition, we measured soluble inorganic and organic P concentrations in fine (1 μm) aerosol fractions and used this data to estimate the contribution of P inputs from dust deposition to the forest P budget. Aerosol dry mass was greater in the dry season (December to April, 5.6-15.7 μg m(-3)) than the wet season (May to November, 3.1-7.1 μg m(-3)). In contrast, soluble P concentrations in the aerosols were lower in the dry season (980-1880 μg P g(-1)) than the wet season (1170-3380 μg P g(-1)). The δ(18)OP of dry-season aerosols resembled that of nearby forest soils (∼19.5‰), suggesting a local origin. In the wet season, when the Trans-Atlantic Saharan dust belt moves north close to Panama, the δ(18)OP of aerosols was considerably lower (∼15.5‰), suggesting a significant contribution of long-distance dust P transport. Using satellite retrieved aerosol optical depth (AOD) and the P concentrations in aerosols we sampled in periods when Saharan dust was evident we estimate that the monthly P input from long distance dust transport during the period with highest Saharan dust deposition is 88 ± 31 g P ha(-1) month(-1), equivalent to between 10 and 29% of the P in monthly litter fall in nearby forests. These findings have important implications for our understanding of modern nutrient budgets and the productivity of tropical forests in the region under future climate scenarios.

High nitrogen deposition in an agricultural ecosystem of Shaanxi, China.

Science.gov (United States)

Liang, Ting; Tong, Yan'an; Liu, Xuejun; Xu, Wen; Luo, Xiaosheng; Christie, Peter

2016-07-01

Atmospheric nitrogen (N) deposition plays an important role in the global N cycle. Data for dry and wet N deposition in agricultural ecosystem of Shaanxi in China is still imperfect; in this study, we continuously measured concentrations and fluxes of dry N deposition from 2010 to 2013 in Yangling district of Shaanxi province and wet N deposition from 2010 to 2012. The average annual concentrations of NH3, NO2, HNO3, particulate ammonium, and nitrate (pNH4 (+) and pNO3 (-)) varied among 3.9-9.1, 6.6-8.0, 1.2-1.4, 3.1-4.3, and 3.3-4.8 μg N m(-3), respectively, with mean values of 6.0, 7.2, 1.3, 3.8, and 4.1 μg N m(-3), respectively, during the entire monitoring period. The annual NH4 (+)-N and NO3 (-)-N concentrations in precipitation ranged 3.9-4.3 and 2.8-3.4 mg N L(-1) with the mean values of 4.1 and 3.3 mg N L(-1). The NH4 (+)-N/NO3 (-)-N ratio in rainfall averaged 1.2. Dry N deposition flux was determined to be 19.2 kg N ha(-1) year(-1) and the wet N deposition flux was 27.2 kg N ha(-1) year(-1). The amount of total atmospheric N deposition (dry plus wet) reached 46.4 kg N ha(-1) year(-1), in which dry deposition accounted 41 %. Gaseous N deposition comprised over 75 % of the dry deposition, and the proportion of oxidized N in dry deposition was equal to the reduced N. Therefore, the results suggest that more stringent regional air pollution control policies are required in the target area and that N deposition is an important nutrient resource from the atmosphere that must be taken into consideration in nutrient management planning of agricultural ecosystems.

The distribution on trees of dry deposited material from the Chernobyl accident

International Nuclear Information System (INIS)

Roed, J.

1988-01-01

The distribution of material from the Chernobyl accident that has been dry deposited on forest trees near Roskilde (Denmark) and on trees in a suburban area of Roskilde are investigated. The dry deposition velocities on the plan-projected area covered by the trees are found and compared with those on paved surfaces. The conclusion is that the deposited material is distributed fairly uniformly on the trees, and that the deposition velocities on trees are more than 10 times higher than on paved surfaces. A bulk deposition constant is defined and proposed to be used for modelling the deposition on trees in an urban environment. This work was supported by the EEC Radiation Protection Programme under contract No. B16-107-DK and by NKA, the Nordic Liaison Committee for Atomic Energy

Atmospheric dispersion and deposition of 131I released from the Hanford Site

International Nuclear Information System (INIS)

Ramsdell, J.V. Jr.; Simonen, C.A.; Burk, K.W.; Stage, S.A.

1996-01-01

Approximately 2.6 x 10 4 TBq (700,000 Ci) of 131 I were released to the air from reactor fuel processing plants on the Hanford Site in southcentral Washington State from December 1944 through December 1949. The Hanford Environmental Dose Reconstruction Project developed a suite of codes to estimate the doses that might have resulted from these releases. The Regional Atmospheric Transport Code for Hanford Emission Tracking (RATCHET) computer code is part of this suite. The RATCHET code implements a Lagrangian-trajectory, Gaussian-puff dispersion model that uses hourly meterological and release rate data to estimate daily time-integrated air concentrations and surface contamination for use, in dose estimates. In this model, iodine is treated as a mixture of three species (inorganic gases, organic gases, and particles). Model deposition parameters are functions of the mixture and meterological conditions. A resistance model is used to calculate dry deposition velocities. Equilibrium between concentrations in the precipitation and the air near the ground is assumed in calculating wet deposition of gases, and irreversible washout of the particles is assumed. RATCHET explicitly treats the uncertainties in model parameters and meteorological conditions. Uncertainties in 131 I release rates and partitioning among the nominal species are treated by varying model input. The results of 100 model runs for December 1944 through December 1949 indicate that monthly average air concentrations and deposition have uncertainties ranging from a factor of two near the center of the time-integrated plume to more than an order of magnitude near the edge. These results indicate that ∼10% of the 131 I released to the atmosphere decayed during transit in the study area, ∼56% was deposited within the study area, and the remaining 34% was transported out of the study area while still in the air

Atmospheric heavy metal deposition accumulated in rural forest soils of southern Scandinavia

DEFF Research Database (Denmark)

Hovmand, Mads Frederik; Kemp, Kaare; Kystol, J.

2008-01-01

Thirty-three years of measurements of atmospheric heavy metal (HM) deposition (bulk precipitation) in Denmark combined with European emission inventories form the basis for calculating a 50-year accumulated atmospheric input to a remote forest plantation on the island of Laesoe. Soil samples taken...... in atmospheric deposition and in soils. The accumulated atmospheric deposition is of the same magnitude as the increase of these metals in the top soil....

Dry deposition of sulfur: a 23-year record for the Hubbard Brook Forest ecosystem

Energy Technology Data Exchange (ETDEWEB)

Likens, G E; Eaton, J S [Inst. of Ecosystem Studies, The New York Botanical Garden, NY (US); Bormann, F H [School of Forestry and Environmental Studies Yale Univ., New Haven, CT (US); Hedin, L O [Dept. of Biology, Yale Univ., New Haven, CT (US); Driscoll, C T [Dept. of Civil and Environmental Engineering, Syracuse, NY (US)

1990-01-01

Dry deposition of S was estimated for watershed-ecosystems of the Hubbard Brook Experimental Forest from 1964-65 through 1986-87. Two approaches, a regression analysis of bulk precipitation inputs and stream outputs and a mass-balance method, gave similar average values for Watershed 6 430 and 410 eq SO{sub 4}{sup =}/ha-yr, respectively, for this 23-year period. Dry deposition contributed about 37% of total S deposition, varying from 12% in 1964-65 to 61% in 1983-84. Long-term data from 'replicated' watershed-ecosystems showed that temporal variability in estimates of dry deposition was considerably greater than spatial (between watersheds) variability.

Effect of deposition temperature and thermal annealing on the dry etch rate of a-C: H films for the dry etch hard process of semiconductor devices

International Nuclear Information System (INIS)

Lee, Seung Moo; Won, Jaihyung; Yim, Soyoung; Park, Se Jun; Choi, Jongsik; Kim, Jeongtae; Lee, Hyeondeok; Byun, Dongjin

2012-01-01

The effect of deposition and thermal annealing temperatures on the dry etch rate of a-C:H films was investigated to increase our fundamental understanding of the relationship between thermal annealing and dry etch rate and to obtain a low dry etch rate hard mask. The hydrocarbon contents and hydrogen concentration were decreased with increasing deposition and annealing temperatures. The I(D)/I(G) intensity ratio and extinction coefficient of the a-C:H films were increased with increasing deposition and annealing temperatures because of the increase of sp 2 bonds in the a-C:H films. There was no relationship between the density of the unpaired electrons and the deposition temperature, or between the density of the unpaired electrons and the annealing temperature. However, the thermally annealed a-C:H films had fewer unpaired electrons compared with the as-deposited ones. Transmission electron microscopy analysis showed the absence of any crystallographic change after thermal annealing. The density of the as-deposited films was increased with increasing deposition temperature. The density of the 600 °C annealed a-C:H films deposited under 450 °C was decreased but at 550 °C was increased, and the density of all 800 °C annealed films was increased. The dry etch rate of the as-deposited a-C:H films was negatively correlated with the deposition temperature. The dry etch rate of the 600 °C annealed a-C:H films deposited at 350 °C and 450 °C was faster than that of the as-deposited film and that of the 800 °C annealed a-C:H films deposited at 350 °C and 450 °C was 17% faster than that of the as-deposited film. However, the dry etch rate of the 550 °C deposited a-C:H film was decreased after annealing at 600 °C and 800 °C. The dry etch rate of the as-deposited films was decreased with increasing density but that of the annealed a-C:H films was not. These results indicated that the dry etch rate of a-C:H films for dry etch hard masks can be further decreased by

Atmospheric deposition of beryllium in Central Europe: comparison of soluble and insoluble fractions in rime and snow across a pollution gradient.

Science.gov (United States)

Bohdalkova, Leona; Novak, Martin; Voldrichova, Petra; Prechova, Eva; Veselovsky, Frantisek; Erbanova, Lucie; Krachler, Michael; Komarek, Arnost; Mikova, Jitka

2012-11-15

Little is known about atmospheric input of beryllium (Be) into ecosystems, despite its highly toxic behavior. For three consecutive winters (2009-2011), we measured Be concentrations in horizontal deposition (rime) and vertical deposition (snow) at 10 remote mountain-top locations in the Czech Republic, Central Europe. Beryllium was determined both in filtered waters, and in HF digests of insoluble particles. Across the sites, soluble Be concentrations in rime were 7 times higher, compared to snow (6.1 vs. 0.9ng·L(-1)). Rime scavenged the pollution-rich lower segments of clouds. The lowest Be concentrations were detected in the soluble fraction of snow. Across the sites, 34% of total Be deposition occurred in the form of soluble (bioavailable) Be, the rest were insoluble particles. Beryllium fluxes decreased in the order: vertical dry deposition insoluble>vertical dry deposition soluble>horizontal deposition soluble>vertical wet deposition insoluble>vertical wet deposition soluble>horizontal deposition insoluble. The average contributions of these Be forms to total deposition were 56, 21, 8, 7, 5 and 3%, respectively. Sites in the northeast were more Be-polluted than the rest of the country with sources of pollution in industrial Silesia. Copyright © 2012 Elsevier B.V. All rights reserved.

Sulfur accumulation and atmospherically deposited sulfate in the Lake States.

Science.gov (United States)

Mark B. David; George Z. Gernter; David F. Grigal; Lewis F. Ohmann

1989-01-01

Characterizes the mass of soil sulfur (adjusted for nitrogen), and atmospherically deposited sulfate along an acid precipitation gradient from Minnesota to Michigan. The relationship of these variables, presented graphically through contour mapping, suggests that patterns of atmospheric wet sulfate deposition are reflected in soil sulfur pools.

Loess as an environmental archive of atmospheric trace element deposition

Science.gov (United States)

Blazina, T.; Winkel, L. H.

2013-12-01

Environmental archives such as ice cores, lake sediment cores, and peat cores have been used extensively to reconstruct past atmospheric deposition of trace elements. These records have provided information about how anthropogenic activities such as mining and fossil fuel combustion have disturbed the natural cycles of various atmospherically transported trace elements (e.g. Pb, Hg and Se). While these records are invaluable for tracing human impacts on such trace elements, they often provide limited information about the long term natural cycles of these elements. An assumption of these records is that the observed variations in trace element input, prior to any assumed anthropogenic perturbations, represent the full range of natural variations. However, records such as those mentioned above which extend back to a maximum of ~400kyr may not capture the potentially large variations of trace element input occurring over millions of years. Windblown loess sediments, often representing atmospheric deposition over time scales >1Ma, are the most widely distributed terrestrial sediments on Earth. These deposits have been used extensively to reconstruct continental climate variability throughout the Quaternary and late Neogene periods. In addition to being a valuable record of continental climate change, loess deposits may represent a long term environmental archive of atmospheric trace element deposition and may be combined with paleoclimate records to elucidate how fluctuations in climate have impacted the natural cycle of such elements. Our research uses the loess-paleosol deposits on the Chinese Loess Plateau (CLP) to quantify how atmospheric deposition of trace elements has fluctuated in central China over the past 6.8Ma. The CLP has been used extensively to reconstruct past changes of East Asian monsoon system (EAM). We present a suite of trace element concentration records (e.g. Pb, Hg, and Se) from the CLP which exemplifies how loess deposits can be used as an

Polycyclic aromatic hydrocarbon (PAH) deposition to and exchange at the air-water interface of Luhu, an urban lake in Guangzhou, China

International Nuclear Information System (INIS)

Li Jun; Cheng Hairong; Zhang Gan; Qi Shihua; Li Xiangdong

2009-01-01

Urban lakes are vulnerable to the accumulation of semivolatile organic compounds, such as PAHs from wet and dry atmospheric deposition. Little was reported on the seasonal patterns of atmospheric deposition of PAHs under Asian monsoon climate. Bulk (dry + wet) particle deposition, air-water diffusion exchange, and vapour wet deposition of PAHs in a small urban lake in Guangzhou were estimated based on a year-round monitoring. The total PAH particle deposition fluxes observed were 0.44-3.46 μg m -2 day -1 . The mean air-water diffusive exchange flux was 20.7 μg m -2 day -1 . The vapour deposition fluxes of PAHs ranged 0.15-8.26 μg m -2 day -1 . Remarkable seasonal variations of particulate PAH deposition, air-water exchange fluxes and vapour wet deposition were influenced by seasonal changes in meteorological parameters. The deposition fluxes were predominantly controlled by the precipitation intensity in wet season whereas by atmospheric concentration in dry season. - The PAH deposition fluxes were predominantly controlled by the precipitation intensity in wet season whereas by atmospheric concentration in dry season

Assessing atmospheric nitrogen deposition to natural and semi-natural ecosystems – experience from Danish studies using the DAMOS system

DEFF Research Database (Denmark)

Hertel, Ole; Geels, Camilla; Frohn, Lise

2013-01-01

and ammonium (reaction products of nitrogen oxides and ammonia), but also dry deposition of other reactive nitrogen compounds (mainly nitrogen oxides in the form of gas phase nitric acid and nitrogen dioxide). In Denmark's environmental management of the sensitive terrestrial ecosystems modelling tools...... are required that account for both the local and the long-range transported contributions. This motivated development of the Danish Ammonia MOdelling System (DAMOS) that has been successfully applied to the assessment of atmospheric nitrogen loadings to sensitive Danish ecosystems. We present here three...... different examples of such assessments. Our results show that ecosystems located in Western Denmark (Case 1) receive the highest loads of atmospheric nitrogen depositions which generally exceed the critical load. This part of the country has the highest livestock density. In the Eastern part of the country...

Air pollution dry deposition: radioisotopes as particles and volatiles

International Nuclear Information System (INIS)

Anon.

1981-01-01

This study focuses on determining volcanic ash and ambient airborne solids concentrations at various sampling sites subsequent to the Mt. St. Helens' eruption in order to develop an experimental basis for models predicting removal of airborne particles and gases by dry deposition onto outdoor surfaces. In addition, deposition rates were determined using dual tracer techniques in the field and in a wind tunnel in the laboratory

Atmospheric heavy metal deposition in Europe estimated by moss analysis

Energy Technology Data Exchange (ETDEWEB)

Ruehling, Aa. [Swedish Environmental Research Inst., Lund (Sweden). Dept. of Ecology

1995-12-31

Atmospheric heavy metal deposition in Europe including 21 countries was monitored in 1990-1992 by the moss technique. This technique is based on the fact that the concentrations of heavy metals in moss are closely correlated to atmospheric deposition. This was the first attempt to map heavy metal deposition in this large area. The objectives of the project were to characterise qualitatively and quantitatively the regional atmospheric deposition pattern of heavy metals in background areas in Europe, to indicate the location of important heavy metal pollution sources and to allow retrospective comparisons with similar studies. The present survey is a follow-up of a joint Danish and Swedish project in 1980 and an extended survey in 1985 within the framework of the Nordic Council of Ministers. In Sweden, heavy-metal deposition was first mapped on a nation-wide scale in 1968-1971 and 1975. (author)

Atmospheric heavy metal deposition in Europe estimated by moss analysis

Energy Technology Data Exchange (ETDEWEB)

Ruehling, Aa [Swedish Environmental Research Inst., Lund (Sweden). Dept. of Ecology

1996-12-31

Atmospheric heavy metal deposition in Europe including 21 countries was monitored in 1990-1992 by the moss technique. This technique is based on the fact that the concentrations of heavy metals in moss are closely correlated to atmospheric deposition. This was the first attempt to map heavy metal deposition in this large area. The objectives of the project were to characterise qualitatively and quantitatively the regional atmospheric deposition pattern of heavy metals in background areas in Europe, to indicate the location of important heavy metal pollution sources and to allow retrospective comparisons with similar studies. The present survey is a follow-up of a joint Danish and Swedish project in 1980 and an extended survey in 1985 within the framework of the Nordic Council of Ministers. In Sweden, heavy-metal deposition was first mapped on a nation-wide scale in 1968-1971 and 1975. (author)

Inorganic nitrogenous air pollutants, atmospheric nitrogen deposition and their potential ecological impacts in remote areas of western North America (Invited)

Science.gov (United States)

Bytnerowicz, A.; Fenn, M. E.; Fraczek, W.; Johnson, R.; Allen, E. B.

2013-12-01

Dry deposition of gaseous inorganic nitrogenous (N) air pollutants plays an important role in total atmospheric N deposition and its ecological effects in the arid and semi-arid ecosystems. Passive samplers and denuder/ filter pack systems have been used for determining ambient concentrations of ammonia (NH3), nitric oxide (NO), nitrogen dioxide (NO2), and nitric acid vapor (HNO3) in the topographically complex remote areas of the western United States and Canada. Concentrations of the measured pollutants varied significantly between the monitoring areas. Highest NH3, NO2 and HNO3 levels occurred in southern California areas downwind of the Los Angeles Basin and in the western Sierra Nevada impacted by emissions from the California Central Valley and the San Francisco Bay area. Strong spatial gradients of N pollutants were also present in southeastern Alaska due to cruise ship emissions and in the Athabasca Oil Sands Region in Canada affected by oil exploitation. Distribution of these pollutants has been depicted by maps generated by several geostatistical methodologies within the ArcGIS Geostatistical Analyst (ESRI, USA). Such maps help to understand spatial and temporal changes of air pollutants caused by various anthropogenic activities and locally-generated vs. long range-transported air pollutants. Pollution distribution maps for individual N species and gaseous inorganic reactive nitrogen (Nr) have been developed for the southern portion of the Sierra Nevada, Lake Tahoe Basin, San Bernardino Mountains, Joshua Tree National Park and the Athabasca Oil Sands Region. The N air pollution data have been utilized for estimates of dry and total N deposition by a GIS-based inferential method specifically developed for understanding potential ecological impacts in arid and semi-arid areas. The method is based on spatial and temporal distribution of concentrations of major drivers of N dry deposition, their surface deposition velocities and stomatal conductance values

Chemical characteristics of atmospheric deposition collected at two ENEA stations near Bologna

International Nuclear Information System (INIS)

Barilli, L.; Olivieri, P.; Salvi, S.; Morselli, L.; Grandi, E.; Ianuccilli, A.

1997-06-01

This article presents the results of the measurements of the water quality in acid rains, collected by a Wet and Dry Sampler in 1994 and in 1995 at two ENEA stations, Brasimone and Bologna town, belonging to the RIDEP network and characterized by different geography and different anthropogenic sources. In the Bologna station from April 95 an innovative sampler DAS (Dry Deposition on Aquatic Surface) has been activated. The monitoring has allowed determining the wet deposition fluxes in both the stations and pointing out the differences between two areas characterized by different topology. Besides the DAS sampler has allowed evaluating the total deposition fluxes (wet and dry deposition) in the Bologna station and comparing them with the ''critical loads'' pertaining to the examined territory

Concentration, size distribution and dry deposition of amines in atmospheric particles of urban Guangzhou, China

Science.gov (United States)

Liu, Fengxian; Bi, Xinhui; Zhang, Guohua; Peng, Long; Lian, Xiufeng; Lu, Huiying; Fu, Yuzhen; Wang, Xinming; Peng, Ping'an; Sheng, Guoying

2017-12-01

Size-segregated PM10 samples were collected in Guangzhou, China during autumn of 2014. Nine amines, including seven aliphatic amines and two heterocyclic amines, were detected using a gas chromatography-mass spectrometer after derivatization by benzenesulfonyl chloride. The total concentration of the nine amines (Ʃamines) was 79.6-140.9 ng m-3 in PM10. The most abundant species was methylamine (MA), which had a concentration of 29.2-70.1 ng m-3. MA, dimethylamine (DMA), diethylamine (DEA) and dibutylamine (DBA) were the predominant amines in the samples and accounted for approximately 80% of Ʃamines in each size segment. Two heterocyclic amines, pyrrolidine (PYR) and morpholine (MOR), were detected in all samples and had average concentrations of 1.14 ± 0.37 and 1.89 ± 0.64 ng m-3, respectively, in particles with aerodynamic diameters ammonium ranged from 0.0068 to 0.0107 in particles with diameters <1.5 μm, and the maximum ratio occurred in the smallest particles (diameter< 0.49 μm). The average dry deposition flux and velocity of Ʃamines in PM10 were 7.9 ± 1.6 μg m-2 d-1 and 0.084 ± 0.0021 cm s-1, respectively. The results of this study provide essential information on the contribution of amines to secondary organic aerosols and dry removal mechanisms in urban areas.

Influence of atmospheric dry deposition of inorganic nutrients on phytoplankton biomass in the coastal Bay of Bengal

Digital Repository Service at National Institute of Oceanography (India)

Yadav, K.; Sarma, V.V.S.S.; Rao, D.B.; DileepKumar, M.

mixing due to weak stratification and wind driven mixing supplies significant amount of nutrients to the surface (Prasanna Kumar and Prasad, 1996; de Sousa et al., 1996). Though strong stratification hinders the vertical supply of nutrients during....C; Mahowald ,N., Lima. I; Feely, R.A., Mackenzie, F.T., et al., 2007.Impact of anthropogenic atmospheric nitrogen and sulfur deposition on ocean acidification and the inorganic carbon system. Proc. Natl. Acad. Sci. USA 104:14580–85. Duce, R. A., et al. 2008...

Atmospheric deposition of polycyclic aromatic hydrocarbons near New England coastal waters

Science.gov (United States)

Golomb, D.; Barry, E.; Fisher, G.; Varanusupakul, P.; Koleda, M.; Rooney, T.

Wet and dry deposition of polycyclic aromatic hydrocarbons (PAHs) was measured at Nahant, Massachusetts, a peninsula jutting into Massachusetts Bay and Wolf Neck, a peninsula jutting into Casco Bay, Maine. Wet deposition (rain and snow) was collected in a funnel which drains into a shielded, temperature controlled receiving bottle. Dry deposition of gaseous and particulate PAHs was collected onto an exposed water surface. PAHs were analyzed by solid phase extraction and gas chromatography-mass spectrometry. Sixteen PAH species were analyzed, ranging from acenaphthylene to coronene. The mean wet deposition rate of the sum of the 16 species is 720 ng m -2 cm -1 precipitation at Nahant, and 831 ng m -2 cm -1 precipitation at Wolf Neck. Wet deposition is attributed to regional PAH emitting sources. Storm patterns appear to bring somewhat higher wet deposition of PAHs to Wolf Neck than to Nahant. The mean dry deposition rate is 95 ng m -2 h -1 at Nahant and 9.3 ng m -2 h -1 at Wolf Neck. The large difference is attributed to the fact that Nahant is close to the urban-industrial metropolitan Boston area and Logan International Airport, whereas Wolf Neck has no major PAH-emitting sources nearby. Individual measurements have an error bracket of ±30%. The Chemical Mass Balance model was used to apportion the dry deposition to source categories. At Nahant, nine samples gave valid statistical attributes with a mean apportionment: jet exhaust 35%, gasoline fueled vehicles 32%, diesel fueled vehicles 17%, wood combustion 13%, others 3%. At Wolf Neck, six samples yielded a mean apportionment: jet exhaust 30%, gasoline vehicles 28%, diesel vehicles 18%, wood combustion 16%, others 8%. There is a considerable variation between the samples. The apportionment is greatly dependent on the quality and selection of the model inputs, i.e. source signatures, which for PAHs are questionable.

Magnitudes and sources of precipitation and dry deposition fluxes of industrial and natural leads to the North Pacific at Enewetak

International Nuclear Information System (INIS)

Settle, D.M.; Patterson, C.C.

1982-01-01

A total atmospheric PB input flux of 7 ng Pb cm - 2 yr - 1 was measured in the North Pacific Easterlies at Enewetak. Parameters used to measure this flux were ratio of dry deposition flux to precipitation flux; Pb/ 210 Pb in precipitation and seawater; 210 Pb flux; washout factor; and Pb concentrations in air, rain, and dry deposition deposits. Relations among these parameters estabilished at Enewetak were used to recompute and comfirm previous estimates of lead fluxes to the oceans (ng Pb cm - 2 yr - 1 ) at the following locations: North Altantic Westerlies, 170; North Pacific Westerlies, 50; and South Pacific Easterlies, 3. Prehistoric lead output fluxes to sediments (ng Pb cm - 2 yr - 1 ) at these locations have been previously measured and were 4 (Enewetak); 30 North Atlantic Westerlies; 3 North Pacific Westerlies; 4 South Pacific Easterlies. These data show that the rates of atmospheric imputs of lead to the oceans vary directly with variations in rates of upwind emission of industrial lead from urban complexes on land. In the North Pacific and North Atlantic, present rates of atmospheric lead inputs are 10-fold greater than prehistoric outputs. In equatorial regions, present inputs and past outputs are more nearly equal. These observations disclose the effects of intense industrial atmospheric emissions of lead in the northern hemisphere westerlies which have overwhelmed prehistoric natural fluxes of lead to the oceans. The average concentration of lead in marine air at Enewetak is 170n pg m - 3 and varies less than a factor of 2 from that mean. One to 15% of this lead comes from seaspray, while the remainder comes from sources on land. About 90% of the seaspray lead is industrial, while 80 to 99% of that originating from land sources is industrial. Concentrations of lead in rain at Enewetak range from 6 to 63 pg/g with a mean value of 28

Interactions between atmospheric circulation, nutrient deposition, and tropical forest primary production (Invited)

Science.gov (United States)

Randerson, J. T.; Chen, Y.; Rogers, B. M.; Morton, D. C.; van der Werf, G.; Mahowald, N. M.

2010-12-01

Tropical forests influence regional and global climate by means of several pathways, including by modifying surface energy exchange and by forming clouds. High levels of precipitation, leaching, and soil weathering limit nutrient availability in these ecosystems. Phosphorus (P) is a key element limiting net primary production, and in some areas, including forests recovering from prior disturbance, nitrogen (N) also may limit some components of production. Here we quantified atmospheric P and N inputs to these forests from fires using satellite-derived estimates of emissions and atmospheric models. In Africa and South America, cross-biome transport of fire-emitted aerosols and reactive N gases from savannas and areas near the deforestation frontier increased deposition of P and N in interior forests. Equatorward atmospheric transport during the dry (fire) season in one hemisphere was linked with surface winds moving toward the inter-tropical convergence zone (ITCZ) in the other hemisphere. Deposition levels were higher in tropical forests in Africa than in South America because of large savanna areas with high levels of fire emissions in both southern and northern Africa. We conclude by describing a potential feedback loop by which equatorward transport of fire emissions, dust, and spores sustains the productivity of tropical forests. We specifically assessed evidence that savanna-to-forest atmospheric transport of nutrients increases forest productivity, height, and rates of evapotranspiration (ET). In parallel, we examined the degree to which increases in ET and surface roughness in tropical forests have the potential to strengthen several components of the Hadley circulation, including deep convection, equatorward return flow (near the surface), and the intensity of seasonal drought in the subtropics (thereby increasing fires). These interactions are important for understanding biogeochemical - climate interactions on millennial timescales and for quantifying how

Removal of Atmospheric Ethanol by Wet Deposition: A Global Flux Estimate

Science.gov (United States)

Felix, J. D. D.; Willey, J. D.; Avery, B.; Thomas, R.; Mullaugh, K.; Kieber, R. J.; Mead, R. N.; Helms, J. R.; Campos, L.; Shimizu, M. S.; Guibbina, F.

2017-12-01

Global ethanol fuel consumption has increased exponentially over the last two decades and the US plans to double annual renewable fuel production in the next five years as required by the renewable fuel standard. Regardless of the technology or feedstock used to produce the renewable fuel, the primary end product will be ethanol. Increasing ethanol fuel consumption will have an impact on the oxidizing capacity of the atmosphere and increase atmospheric concentrations of the secondary pollutant peroxyacetyl nitrate as well a variety of VOCs with relatively high ozone reactivities (e.g. ethanol, formaldehyde, acetaldehyde). Despite these documented effects of ethanol emissions on atmospheric chemistry, current global atmospheric ethanol budget models have large uncertainties in the magnitude of ethanol sources and sinks. The presented work investigates the global wet deposition sink by providing the first estimate of the global wet deposition flux of ethanol (2.4 ± 1.6 Tg/yr) based on empirical wet deposition data (219 samples collected at 12 locations). This suggests the wet deposition sink removes between 6 and 17% of atmospheric ethanol annually. Concentrations of ethanol in marine wet deposition (25 ± 6 nM) were an order of magnitude less than in the majority of terrestrial deposition (345 ± 280 nM). Terrestrial deposition collected in locations impacted by high local sources of biofuel usage and locations downwind from ethanol distilleries were an order of magnitude higher in ethanol concentration (3090 ± 448 nM) compared to deposition collected in terrestrial locations not impacted by these sources. These results indicate that wet deposition of ethanol is heavily influenced by local sources and ethanol emission impacts on air quality may be more significant in highly populated areas. As established and developing countries continue to rapidly increase ethanol fuel consumption and subsequent emissions, understanding the magnitude of all ethanol sources and

Modeling Dry Deposition of Aerosol Particles on Rough Surfaces

Czech Academy of Sciences Publication Activity Database

Hussein, T.; Smolík, Jiří; Kerminen, V.-M.; Kulmala, M.

2012-01-01

Roč. 46, č. 1 (2012), s. 44-59 ISSN 0278-6826 Institutional research plan: CEZ:AV0Z40720504 Keywords : aerosol particles * dry deposition * transport Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 2.780, year: 2012

Effects of atmospheric inorganic nitrogen deposition on ocean biogeochemistry

OpenAIRE

Krishnamurthy, Aparna; Moore, J. Keith; Zender, Charles S; Luo, Chao

2007-01-01

 We perform a sensitivity study with the Biogeochemical Elemental Cycling (BEC) ocean model to understand the impact of atmospheric inorganic nitrogen deposition on marine biogeochemistry and air-sea CO2 exchange. Simulations involved examining the response to three different atmospheric inorganic nitrogen deposition scenarios namely, Pre-industrial (22 Tg N/year), 1990s (39 Tg N/year), and an Intergovernmental Panel on Climate Change (IPCC) prediction for 2100, IPCC-A1FI (69 Tg N/year). Glob...

Dry deposition of radionuclides on leafy vegetables

International Nuclear Information System (INIS)

Heuberger, H.; Tschiersch, J.; Shinonaga, T.; Bunzl, K.; Pliml, A.; Dietl, F.; Keusch, M.

2004-01-01

The dry deposition of gaseous elemental radio-iodine and particulate radio-caesium on mature leafy vegetable was studied in chamber experiments. The simultaneous exposition of endive, head lettuce, red oak leaf lettuce and spinach (spring leafy vegetable) rsp. curly kale, white cabbage and spinach (summer leafy vegetable) was performed under homogeneous and controlled conditions. The sample collective of each species was such large that for the expected variation of the results a statistically firm analysis was possible. Significant differences were observed for the 131 I deposition on spring vegetable: the deposition on spinach was roughly 3times that on leaf lettuce, 4times that on endive and 9times that on head lettuce. For 134 Cs, there was no significant difference between spinach and leaf lettuce, about twice the amount was deposited on both species as on endive and 3times as on head lettuce. All summer vegetables showed differences in deposition. For lodine, the deposition on spinach was roughly 3times (6times) that on curly kale and 35times (100times) that on white cabbage in the 2 experiments. For caesium, the deposition to curly kale was highest, about twice that on spinach and 35times (80times) that on white cabbage. The deposition velocity could be estimated, in average it was about 8times higher for 131 I than for 134 Cs. The influence of the particle size on the deposition velocity was small in the considered size range. Washing could reduce the contamination by about 10% for 131 I and 45% for 134 Cs. (orig.)

Atmospheric deposition, operational report for air pollution 2003. NOVA 2003; Atmosfaerisk deposition, driftsrapport for Luftforurening i 2003 NOVA 2003

Energy Technology Data Exchange (ETDEWEB)

Ellermann, T.; Hertel, O.; Ambelas Skjoeth, C.; Kemp, K.; Monies, C.

2004-12-01

This report presents measurements and calculations from the atmospheric part of NOVA 2003 and covers results for 2003. It summarises the main results concerning concentrations and depositions of nitrogen, phosphorous and sulphur compounds related to eutrofication and acidification and selected heavy metals. Depositions of atmospheric compounds to Danish marine waters as well as land surface are presented. The measurements in the monitoring programme are supplemented with model calculations of concentrations and depositions of nitrogen and sulphur compounds to Danish land surfaces as well as marine waters, fjords and bays using the ACDEP model (Atmospheric Chemistry and Deposition). The model is a so-called trajectory model and simulates the physical and chemical processes in the atmosphere using meteorological and emission data input. (BA)

Litterfall mercury dry deposition in the eastern USA

Science.gov (United States)

Martin R. Risch; John F. DeWild; David P. Krabbenhoft; Randall K. Kolka; Leiming. Zhang

2012-01-01

Mercury (Hg) in autumn litterfall frompredominately deciduous forestswas measured in 3 years of samples from 23 Mercury Deposition Network sites in 15 states across the eastern USA. Annual litterfall Hg dry depositionwas significantly higher (median 12.3 micrograms per square meter (µg/m2), range 3.5-23.4 µg/m2...

Studies of dry deposition of trace elements and diesel soot onto Lake Michigan and the Chesapeake Bay

International Nuclear Information System (INIS)

Ondov, J.M.; Caffrey, P.F.; Suarez, A.E.; Han, M.; Borgoul, P.V.

1995-01-01

As part of the Atmospheric Exchange Over Lakes and Oceans Study (AEOLOS) study, the University of Maryland participated in four intensive field campaigns, three on Lake Michigan (LM) and one on the Chesapeake Bay (CB), to determine the size distributions of potentially toxic elemental aerosol constituents, determine their sources, and their dry deposition loadings to surface waters. The work further seeks to elucidate the relative importance of constituents of fine- and coarse particles, as differentiation of these modes is essential to the eventual formation of control strategies. Unique components of the UMCP studies include (1) resolution of toxic elemental components of aerosol particles depositing to LM and CB by particle size and by source and (2) a Lake-wide evaluation of the importance of fine and coarse particle deposition to inorganic contamination of LM surface waters. In addition, a unique component of the Baltimore Study was the application of a sensitive iridium tracer to intentionally tag emissions form the City of Baltimore's sanitation truck fleet to tag the Baltimore urban plume and to determine the atmospheric behavior of diesel soot particles, a major source of urban carbon aerosol and the principle carrier of toxic polynuclear aromatic hydrocarbons. The work encompasses results for >40 elements by X-ray fluorescence and instrumental neutron activation analyses of more than 700 individual size-segregated aerosol, deposition, urban dust, and surface-water-suspended particulate samples. An overview of the results of these studies will be presented

Surface deposition from radioactive plumes

International Nuclear Information System (INIS)

Garland, J.A.

1980-01-01

Accidents involving nuclear plants may release radioactive particles and gases to the atmosphere. Dry deposition of particles has been investigated mainly in the laboratory and a general understanding of the transfer mechanisms has been established. However there is apparently a substantial discrepancy between the few field observations of dry deposition of particles and laboratory measurements, particularly for 0.1 - 1 μm particles for which laboratory work shows very small deposition rates. In addition there are few estimates of deposition rates for forest and some other kinds of terrain. The most important gas in the context of a nuclear accident is I-131 and the behaviour of this gas at grass surfaces has received much attention. However smaller quantities of other gases and vapours may be released and the surface absorption of these species may require further investigation. In addition there is little knowledge of the behaviour of gases over many types of surface. The rate of deposition of particles and gases is influenced by many parameters including wind speed and the temperature stratification of the lower atmosphere. Conditions which give poor atmospheric dispersion usually give lower deposition velocities. Transfer to man depends on the availability of deposited materials on crops and grass. A wide range of isotopes including iodine and several metallic fission products are lost with a half life for residence on grass ranging from a few days to a few tens days, depending on climatic conditions

Atmospheric deposition and soil vertical distribution of {sup 7}Be in a semiarid region of central Argentina

Energy Technology Data Exchange (ETDEWEB)

Lohaiza, Flavia A.; Velasco, Hugo; Ayub, Jimena Juri; Rizzotto, Marcos; Valladares, Diego L. [Grupo de Estudios Ambientales, Instituto de Matematica Aplicada San Luis, Universidad Nacional de San Luis - CONICET, Ejercito de los Andes 950, D5700HHW San Luis (Argentina)

2014-07-01

Beryllium-7 is a potentially powerful tracer of soil erosion but poor information on {sup 7}Be atmospheric deposition and associated soil inventories in a semiarid region of Central Argentina exists. We estimated the {sup 7}Be atmospheric wet deposition and {sup 7}Be inventory in undisturbed soils north of the City of San Luis (S 33 deg. 9'; W 66 deg. 16') and explored its seasonal variation. Rain and soil samples were collected during 2006-2008 and 2009-2012, respectively. The atmospheric wet deposition was estimated considering both the mean activity concentration in rainwater and the precipitation regime of the region. Using the assessed monthly wet deposition of {sup 7}Be, the expected {sup 7}Be areal activity in soil was estimated applying a simple model. These estimated values were confronted with the experimental measurements in soil. The {sup 7}Be rainwater activity concentration ranged from 0.7 to 3.2 Bq l{sup -1}, with a mean of 1.7 Bq l{sup -1} (sd = 0.53 Bq l{sup -1}). A good linear relationship between {sup 7}Be wet deposition and rain magnitude was obtained (R=0.92, p<0.0001). The wet deposition on soil ranged from 1.1 to 120 Bq m{sup -2} with a mean value of 32.7 Bq m-2 (sd = 29.9 Bq m-2). The annual depositional flux was estimated at 1140 ± 120 Bq m{sup -2} y{sup -1}. The {sup 7}Be mass activity (Bq kg{sup -1}) values in soil samples in the wet period (November-April) were higher than in the dry period (May-October). A typical decreasing exponential function of {sup 7}Be areal activity (Bq m{sup -2}) with soil mass depth (kg m{sup -2}) was found and the distribution parameters for each month were determined. The minimum value of areal activity was 51 Bq m{sup -2} in August, reaching the maximum of 438 Bq m{sup -2} in February. The relaxation mass depth ranged from 2.9 kg m{sup -2} in March to 1.3 kg m{sup -2} in August. The confrontation of experimental measurements in soil with the estimated values using the model showed a good agreement

Deposition rates of viruses and bacteria above the atmospheric boundary layer.

Science.gov (United States)

Reche, Isabel; D'Orta, Gaetano; Mladenov, Natalie; Winget, Danielle M; Suttle, Curtis A

2018-04-01

Aerosolization of soil-dust and organic aggregates in sea spray facilitates the long-range transport of bacteria, and likely viruses across the free atmosphere. Although long-distance transport occurs, there are many uncertainties associated with their deposition rates. Here, we demonstrate that even in pristine environments, above the atmospheric boundary layer, the downward flux of viruses ranged from 0.26 × 10 9 to >7 × 10 9  m -2 per day. These deposition rates were 9-461 times greater than the rates for bacteria, which ranged from 0.3 × 10 7 to >8 × 10 7  m -2 per day. The highest relative deposition rates for viruses were associated with atmospheric transport from marine rather than terrestrial sources. Deposition rates of bacteria were significantly higher during rain events and Saharan dust intrusions, whereas, rainfall did not significantly influence virus deposition. Virus deposition rates were positively correlated with organic aerosols 0.7 μm, implying that viruses could have longer residence times in the atmosphere and, consequently, will be dispersed further. These results provide an explanation for enigmatic observations that viruses with very high genetic identity can be found in very distant and different environments.

Dry deposition and resuspension of particulate matter in city environments

International Nuclear Information System (INIS)

Jensen, N.O.

1984-06-01

The report describes, mostly in qualitative terms, the deposition and resuspension of particles and how the mechanics depend on particle size. The effect of rough surfaces is discussed. It is concluded that knowledge on the subject, at relevant large Reynolds numbers, is indeed lacking. Various methods for measurements of deposition is mentioned and further the report gives some general ideas on how a suitable full scale experiment should be laid out in order to produce some data on the problems of dry deposition to city surfaces. (author)

Mechanistic study of aerosol dry deposition on vegetated canopies

International Nuclear Information System (INIS)

Petroff, A.

2005-04-01

The dry deposition of aerosols onto vegetated canopies is modelled through a mechanistic approach. The interaction between aerosols and vegetation is first formulated by using a set of parameters, which are defined at the local scale of one surface. The overall deposition is then deduced at the canopy scale through an up-scaling procedure based on the statistic distribution parameters. This model takes into account the canopy structural and morphological properties, and the main characteristics of the turbulent flow. Deposition mechanisms considered are Brownian diffusion, interception, initial and turbulent impaction, initially with coniferous branches and then with entire canopies of different roughness, such as grass, crop field and forest. (author)

A MULTILAYER BIOCHEMICAL DRY DEPOSITION MODEL 2. MODEL EVALUATION

Science.gov (United States)

The multilayer biochemical dry deposition model (MLBC) described in the accompanying paper was tested against half-hourly eddy correlation data from six field sites under a wide range of climate conditions with various plant types. Modeled CO2, O3, SO2<...

Deposition of atmospheric 210Pb and total beta activity in Finland

International Nuclear Information System (INIS)

Jussi Paatero; Murat Buyukay; Juha Hatakka; Kaisa Vaaramaa; Jukka Lehto

2015-01-01

The seasonal and regional variation of the atmospheric 210 Pb deposition in Finland was studied. The 210 Pb activity concentration in precipitation shows a decreasing trend from southeastern Finland north-westwards. An average deposition of 40 Bq/m 2 during a 12 months period was observed. The deposition of 210 Pb shows a seasonal variation with minimum in spring and maximum in autumn and winter. The specific activity of 210 Pb (activity of 210 Pb per unit mass of stable lead) in the atmosphere has returned to the level prior to World War II owing to the reduced lead emissions into the atmosphere. (author)

Atmospheric deposition as an important nitrogen load to a typical agro-ecosystem in the Huang-Huai-Hai Plain. 2. Seasonal and inter-annual variations and their implications (2008-2012)

Science.gov (United States)

Huang, Ping; Zhang, Jiabao; Ma, Donghao; Wen, Zhaofei; Wu, Shengjun; Garland, Gina; Pereira, Engil Isadora Pujol; Zhu, Anning; Xin, Xiuli; Zhang, Congzhi

2016-03-01

Atmospheric nitrogen (N) deposition, an important N source to agro-ecosystems, has increased intensively in China during recent decades. However, knowledge on temporal variations of total N deposition and their influencing factors is limited due to lack of systematic monitoring data. In this study, total N deposition, including dry and wet components, was monitored using the water surrogate surface method for a typical agro-ecosystem with a winter wheat (Triticum aestivum L.) and summer maize (Zea mays L.) rotation system in the Huang-Huai-Hai Plain from May 2008 to April 2012. The results indicated that annual total N deposition ranged from 23.8 kg N ha-1 (2009-2010) to 40.3 kg N ha-1 (2008-2009) and averaged 31.8 kg N ha-1. Great inter-annual variations were observed during the sampling period, due to differences in annual rainfall and gaseous N losses from farmlands. Monthly total N deposition varied greatly, from less than 0.6 kg N ha-1 (January, 2010) to over 8.0 kg N ha-1 (August, 2008), with a mean value of 2.6 kg N ha-1. In contrast to wet deposition, dry portions generally contributed more to the total, except in the precipitation-intensive months, accounting for 65% in average. NH4+ -N was the dominant species in N deposition and its contribution to total deposition varied from 6% (December, 2009) to 79% (July, 2008), averaging 53%. The role of organic N (O-N) in both dry and wet deposition was equal to or even greater than that of NO3- -N. Influencing factors such as precipitation and its seasonal distribution, reactive N sources, vegetation status, field management practices, and weather conditions were responsible for the temporal variations of atmospheric N deposition and its components. These results are helpful for reducing the knowledge gaps in the temporal variations of atmospheric N deposition and their influencing factors in different ecosystems, to improve the understandings on N budget in the typical agro-ecosystem, and to provide references

Spatial variation in the flux of atmospheric deposition and its ecological effects in arid Asia

Science.gov (United States)

Jiao, Linlin; Wang, Xunming; Li, Danfeng

2018-06-01

Atmospheric deposition is one of the key land surface processes, and plays important roles in regional ecosystems and global climate change. Previous studies have focused on the magnitude of and the temporal and spatial variations in the flux of atmospheric deposition, and the composition of atmospheric deposition on a local scale. However, there have been no comprehensive studies of atmospheric deposition on a regional scale and its ecological effects in arid Asia. The temporal and spatial patterns, composition of atmospheric deposition, and its potential effects on regional ecosystems in arid Asia are investigated in this study. The results show that the annual deposition flux is high on the Turan Plain, Aral Sea Desert, and Tarim Basin. The seasonal deposition flux also varies remarkably among different regions. The Tarim Basin shows higher deposition flux in both spring and summer, southern Mongolian Plateau has a higher deposition flux in spring, and the deposition flux of Iran Plateau is higher in summer. Multiple sources of elements in deposited particles are identified. Calcium, iron, aluminum, and magnesium are mainly derived from remote regions, while zinc, copper and lead have predominantly anthropogenic sources. Atmospheric deposition can provide abundant nutrients to vegetation and consequently play a role in the succession of regional ecosystems by affecting the structure, function, diversity, and primary production of the vegetation, especially the exotic or short-lived opportunistic species in arid Asia. Nevertheless, there is not much evidence of the ecological effects of atmospheric deposition on the regional and local scale. The present results may help in further understanding the mechanism of atmospheric deposition as well as providing a motivation for the protection of the ecological environment in arid Asia.

Dry Deposition of Reactive Nitrogen From Satellite Observations of Ammonia and Nitrogen Dioxide Over North America

Science.gov (United States)

Kharol, S. K.; Shephard, M. W.; McLinden, C. A.; Zhang, L.; Sioris, C. E.; O'Brien, J. M.; Vet, R.; Cady-Pereira, K. E.; Hare, E.; Siemons, J.; Krotkov, N. A.

2018-01-01

Reactive nitrogen (Nr) is an essential nutrient to plants and a limiting element for growth in many ecosystems, but it can have harmful effects on ecosystems when in excess. Satellite-derived surface observations are used together with a dry deposition model to estimate the dry deposition flux of the most abundant short-lived nitrogen species, NH3 and NO2, over North America during the 2013 warm season. These fluxes demonstrate that the NH3 contribution dominates over NO2 for most regions (comprising 85% of their sum in Canada and 65% in the U.S.), with some regional exceptions (e.g. Alberta and northeastern U.S.). Nationwide, 51 t of N from these species were dry deposited in the U.S., approximately double the 28 t in Canada over this period. Forest fires are shown to be the major contributor of dry deposition of Nr from NH3 in northern latitudes, leading to deposition fluxes 2-3 times greater than from expected amounts without fires.

Sulphur and nitrogen in the atmosphere

International Nuclear Information System (INIS)

Legge, A.H.

1990-01-01

The author discusses sulfur and nitrogen compounds in the atmosphere. Both dry and wet deposition of these compounds are reported on. Characteristics of air pollutant exposure dynamics are described. Environmental responses to the deposition of sulfur and nitrogen compounds, as well as to other pollutants, are detailed

The annual averaged atmospheric dispersion factor and deposition factor according to methods of atmospheric stability classification

Energy Technology Data Exchange (ETDEWEB)

Jeong, Hae Sun; Jeong, Hyo Joon; Kim, Eun Han; Han, Moon Hee; Hwang, Won Tae [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

2016-09-15

This study analyzes the differences in the annual averaged atmospheric dispersion factor and ground deposition factor produced using two classification methods of atmospheric stability, which are based on a vertical temperature difference and the standard deviation of horizontal wind direction fluctuation. Daedeok and Wolsong nuclear sites were chosen for an assessment, and the meteorological data at 10 m were applied to the evaluation of atmospheric stability. The XOQDOQ software program was used to calculate atmospheric dispersion factors and ground deposition factors. The calculated distances were chosen at 400 m, 800 m, 1,200 m, 1,600 m, 2,400 m, and 3,200 m away from the radioactive material release points. All of the atmospheric dispersion factors generated using the atmospheric stability based on the vertical temperature difference were shown to be higher than those from the standard deviation of horizontal wind direction fluctuation. On the other hand, the ground deposition factors were shown to be same regardless of the classification method, as they were based on the graph obtained from empirical data presented in the Nuclear Regulatory Commission's Regulatory Guide 1.111, which is unrelated to the atmospheric stability for the ground level release. These results are based on the meteorological data collected over the course of one year at the specified sites; however, the classification method of atmospheric stability using the vertical temperature difference is expected to be more conservative.

Chemically and size-resolved particulate matter dry deposition on stone and surrogate surfaces inside and outside the low emission zone of Milan: application of a newly developed "Deposition Box".

Science.gov (United States)

Ferrero, Luca; Casati, Marco; Nobili, Lara; D'Angelo, Luca; Rovelli, Grazia; Sangiorgi, Giorgia; Rizzi, Cristiana; Perrone, Maria Grazia; Sansonetti, Antonio; Conti, Claudia; Bolzacchini, Ezio; Bernardi, Elena; Vassura, Ivano

2018-04-01

The collection of atmospheric particles on not-filtering substrates via dry deposition, and the subsequent study of the particle-induced material decay, is trivial due to the high number of variables simultaneously acting on the investigated surface. This work reports seasonally resolved data of chemical composition and size distribution of particulate matter deposed on stone and surrogate surfaces obtained using a new method, especially developed at this purpose. A "Deposition Box" was designed allowing the particulate matter dry deposition to occur selectively removing, at the same time, variables that can mask the effect of airborne particles on material decay. A pitched roof avoided rainfall and wind variability; a standardised gentle air exchange rate ensured a continuous "sampling" of ambient air leaving unchanged the sampled particle size distribution and, at the same time, leaving quite calm condition inside the box, allowing the deposition to occur. Thus, the "Deposition Box" represents an affordable tool that can be used complementary to traditional exposure systems. With this system, several exposure campaigns, involving investigated stone materials (ISMs) (Carrara Marble, Botticino limestone, Noto calcarenite and Granite) and surrogate (Quartz, PTFE, and Aluminium) substrates, have been performed in two different sites placed in Milan (Italy) inside and outside the low emission zone. Deposition rates (30-90 μg cm -2  month -1 ) showed significant differences between sites and seasons, becoming less evident considering long-period exposures due to a positive feedback on the deposition induced by the deposited particles. Similarly, different stone substrates influenced the deposition rates too. The collected deposits have been observed with optical and scanning electron microscopes and analysed by ion chromatography. Ion deposition rates were similar in the two sites during winter, whereas it was greater outside the low emission zone during summer and

The use of a large-strain consolidation model to optimise multilift tailing deposits

NARCIS (Netherlands)

Vardon, P.J.; Yao, Y.; Van Paassen, L.A.; Van Tol, A.F.

2015-01-01

Thin-lift atmospheric fine drying (AFD) is a technique used to dewater mine and oil sand tailings, which utilises both self-weight consolidation and atmospheric evaporation. The disposed layers undergo a cyclic drying and rewetting process due to precipitation and deposition of additional lifts on

Note: Influence of rinsing and drying routines on growth of multilayer thin films using automated deposition system.

Science.gov (United States)

Gamboa, Daniel; Priolo, Morgan A; Ham, Aaron; Grunlan, Jaime C

2010-03-01

A versatile, high speed robot for layer-by-layer deposition of multifunctional thin films, which integrates concepts from previous dipping systems, has been designed with dramatic improvements in software, positioning, rinsing, drying, and waste removal. This system exploits the electrostatic interaction of oppositely charged species to deposit nanolayers (1-10 nm thick) from water onto the surface of a substrate. Dip times and number of deposited layers are adjustable through a graphical user interface. In between dips the system spray rinses and dries the substrate by positioning it in the two-tiered rinse-dry station. This feature significantly reduces processing time and provides the flexibility to choose from four different procedures for rinsing and drying. Assemblies of natural montmorillonite clay and polyethylenimine are deposited onto 175 microm poly(ethylene terephthalate) film to demonstrate the utility of this automated deposition system. By altering the type of rinse-dry procedure, these clay-based assemblies are shown to exhibit variations in film thickness and oxygen transmission rate. This type of system reproducibly deposits films containing 20 or more layers and may also be useful for other types of coatings that make use of dipping.

Dry deposition on smooth and rough urban surfaces

International Nuclear Information System (INIS)

Roed, J.

1987-01-01

Following the Chernobyl accident, dry deposition velocities on smooth surfaces indoors and outdoors have been measured in Denmark. Internal wall surfaces gave deposition velocities of 0.0008-0.0009 cm/s for 131I and 0.0001-0.0002 cm/s for 134Cs and 103Ru. Internal floor surfaces gave higher values for the deposition velocities: for 131I, 0.002 cm/s and for 134Cs and 103Ru, 0.0005-0.0013 cm/s. The deposition velocities on vertical and horizontal external surfaces were nearly equal. Those for 131I were found as 0.02-0.03 cm/s and for 137Cs as 0.001-0.002 cm/s. On external rough surfaces such as grass and corrugated roof material the deposition velocities for 134Cs and 103Ru were 0.03-0.05 cm/s. For iodine, however, deposition velocities were higher for clipped grass (2 cm/s) than for roof material (0.2-0.4 cm/s). The results show that internal deposition velocities are considerably lower than those on external smooth surfaces, and that the deposition velocities on rough surfaces are an order of magnitude higher than on smooth surfaces. It was also shown that the deposition velocities of iodine are considerably higher than those of cesium and ruthenium. This work was supported by EEC Radiation Protection Programme No B16-107-DK and by NKA, The Nordic Liaison Committee for Atomic Energy. (author)

Trends in the chemistry of atmospheric deposition and surface waters in the Lake Maggiore catchment

Directory of Open Access Journals (Sweden)

M. Rogora

2001-01-01

Full Text Available The Lake Maggiore catchment is the area of Italy most affected by acid deposition. Trend analysis was performed on long-term (15-30 years series of chemical analyses of atmospheric deposition, four small rivers draining forested catchments and four high mountain lakes. An improvement in the quality of atmospheric deposition was detected, due to decreasing sulphate concentration and increasing pH. Similar trends were also found in high mountain lakes and in small rivers. Atmospheric deposition, however, is still providing a large and steady flux of nitrogen compounds (nitrate and ammonium which is causing increasing nitrogen saturation in forest ecosystems and increasing nitrate levels in rivers. Besides atmospheric deposition, an important factor controlling water acidification and recovery is the weathering of rocks and soils which may be influenced by climate warming. A further factor is the episodic deposition of Saharan calcareous dust which contributes significantly to base cation deposition. Keywords: trend, atmospheric deposition, nitrogen, stream water chemistry.

Nitrogen mineralization across an atmospheric nitrogen deposition gradient in Southern California deserts

Science.gov (United States)

L.E. Rao; D.R. Parker; Andrzej Bytnerowicz; E.B. Allen

2009-01-01

Dry nitrogen deposition is common in arid ecosystems near urban and agricultural centers, yet its impacts on natural environments are relatively understudied. We examined the effects of N deposition on soil N mineralization across a depositional gradient at Joshua Tree National Park. We hypothesized that N deposition affects N mineralization by promoting...

Spatial atmospheric atomic layer deposition of alxzn1-xo

NARCIS (Netherlands)

Illiberi, A.; Scherpenborg, R.; Wu, Y.; Roozeboom, F.; Poodt, P.

2013-01-01

The possibility of growing multicomponent oxides by spatial atmospheric atomic layer deposition has been investigated. To this end, Al xZn1-xO films have been deposited using diethyl zinc (DEZ), trimethyl aluminum (TMA), and water as Zn, Al, and O precursors, respectively. When the metal precursors

Trade-Induced Atmospheric Mercury Deposition over China and Implications for Demand-Side Controls.

Science.gov (United States)

Chen, Long; Meng, Jing; Liang, Sai; Zhang, Haoran; Zhang, Wei; Liu, Maodian; Tong, Yindong; Wang, Huanhuan; Wang, Wei; Wang, Xuejun; Shu, Jiong

2018-02-20

Mercury (Hg) is of global concern because of its adverse effects on humans and the environment. In addition to long-range atmospheric transport, Hg emissions can be geographically relocated through economic trade. Here, we investigate the effect of China's interregional trade on atmospheric Hg deposition over China, using an atmospheric transport model and multiregional input-output analysis. In general, total atmospheric Hg deposition over China is 408.8 Mg yr -1 , and 32% of this is embodied in China's interregional trade, with the hotspots occurring over Gansu, Henan, Hebei, and Yunnan provinces. Interprovincial trade considerably redistributes atmospheric Hg deposition over China, with a range in deposition flux from -104% to +28%. Developed regions, such as the Yangtze River Delta (Shanghai, Jiangsu, and Zhejiang) and Guangdong, avoid Hg deposition over their geographical boundaries, instead causing additional Hg deposition over developing provinces. Bilateral interaction among provinces is strong over some regions, suggesting a need for joint mitigation, such as the Jing-Jin-Ji region (Beijing, Tianjin, and Hebei) and the Yangtze River Delta. Transferring advanced technology from developed regions to their developing trade partners would be an effective measure to mitigate China's Hg pollution. Our findings are relevant to interprovincial efforts to reduce trans-boundary Hg pollution in China.

Instrumental neutron activation analysis of dry atmospheric fall-out and rain-water

International Nuclear Information System (INIS)

Schutyser, P.; Maenhaut, W.; Dams, R.

1978-01-01

An automated precipitation sampler and an instrumental neutron activation analysis (i.n.a.a.) method for the determination of some major and trace elements in dry atmospheric fall-out and rain-water are presented. The sampler features a rain detector which makes separate collections of dry atmospheric fall-out and rain-water possible. The sampler is equipped with u.v. lamps in order to avoid algal growth during extended collection periods. After collection, the samples are separated into water-soluble and insoluble fractions. The soluble fraction is preconcentrated before analysis by freeze-drying. The i.n.a.a. method involves the measurement of both short- and long-lived radioactivities so that a total of 35 elements can be determined. The possibility of losses during freeze-drying and the accuracy of the i.n.a.a. method were investigated for 7 elements by analysis of a soluble fraction with an independent method, viz. inductively coupled plasma atomic emission spectrometry. (Auth.)

Microorganisms and heavy metals associated with atmospheric deposition in a congested urban environment of a developing country: Sri Lanka.

Science.gov (United States)

Weerasundara, Lakshika; Amarasekara, R W K; Magana-Arachchi, D N; Ziyath, Abdul M; Karunaratne, D G G P; Goonetilleke, Ashantha; Vithanage, Meththika

2017-04-15

The presence of bacteria and heavy metals in atmospheric deposition were investigated in Kandy, Sri Lanka, which is a typical city in the developing world with significant traffic congestion. Atmospheric deposition samples were analyzed for Al, Cr, Mn, Fe, Ni, Cu, Zn, Cd and Pb which are heavy metals common to urban environments. Al and Fe were found in high concentrations due to the presence of natural sources, but may also be re-suspended by vehicular traffic. Relatively high concentrations of toxic metals such as Cr and Pb in dissolved form were also found. High Zn loads can be attributed to vehicular emissions and the wide use of Zn coated roofing materials. The metal loads in wet deposition showed higher concentrations compared to dry deposition. The metal concentrations among the different sampling sites significantly differ from each other depending on the traffic conditions. Industrial activities are not significant in Kandy City. Consequently, the traffic exerts high influence on heavy metal loadings. As part of the bacterial investigations, nine species of culturable bacteria, namely; Sphingomonas sp., Pseudomonas aeruginosa, Pseudomonas monteilii, Klebsiella pneumonia, Ochrobactrum intermedium, Leclercia adecarboxylata, Exiguobacterium sp., Bacillus pumilus and Kocuria kristinae, which are opportunistic pathogens, were identified. This is the first time Pseudomonas monteilii and Ochrobactrum intermedium has been reported from a country in Asia. The culturable fraction constituted ~0.01 to 10%. Pigmented bacteria and endospore forming bacteria were copious in the atmospheric depositions due to their capability to withstand harsh environmental conditions. The presence of pathogenic bacteria and heavy metals creates potential human and ecosystem health risk. Copyright © 2017 Elsevier B.V. All rights reserved.

The theory of the interaction of atmospheric aerosol with underlying surface

International Nuclear Information System (INIS)

Buikov, M.V.

1993-01-01

The interaction of wind with underlying surfaces through resuspension makes a great contribution to the total amount of atmospheric aerosols. The dry deposition process results in cleaning of the atmosphere and contamination of near-surface air layers of soil and vegetation. This paper examines the theory leading to an exact solution of the problem of turbulent transportation of pollution taking into account resuspension and dry-deposition. This may be useful for the interpretation of observational data and for the improvement of calculation methods to describe aerosol exchange at surfaces in air. (author)

Development of ion-exchange collectors for monitoring atmospheric deposition of inorganic pollutants in Alaska parklands

Science.gov (United States)

Brumbaugh, William G.; Arms, Jesse W.; Linder, Greg L.; Melton, Vanessa D.

2016-09-19

Between 2010 and 2014, the U.S. Geological Survey completed a series of laboratory and field experiments designed to develop methodology to support the National Park Service’s long-term atmospheric pollutant monitoring efforts in parklands of Arctic Alaska. The goals of this research were to develop passive sampling methods that could be used for long-term monitoring of inorganic pollutants in remote areas of arctic parklands and characterize relations between wet and dry deposition of atmospheric pollutants to that of concentrations accumulated by mosses, specifically the stair-step, splendid feather moss, Hylocomium splendens. Mosses and lichens have been used by National Park Service managers as atmospheric pollutant biomonitors since about 1990; however, additional research is needed to better characterize the dynamics of moss bioaccumulation for various classes of atmospheric pollutants. To meet these research goals, the U.S. Geological Survey investigated the use of passive ionexchange collectors (IECs) that were adapted from the design of Fenn and others (2004). Using a modified IEC configuration, mulitple experiments were completed that included the following: (a) preliminary laboratory and development testing of IECs, (b) pilot-scale validation field studies during 2012 with IECs at sites with instrumental monitoring stations, and (c) deployment of IECs in 2014 at sites in Alaska having known or suspected regional sources of atmospheric pollutants where samples of Hylocomium splendens moss also could be collected for comparison. The targeted substances primarily included ammonium, nitrate, and sulfate ions, and certain toxicologically important trace metals, including cadmium, cobalt, copper, nickel, lead, and zinc.Deposition of atmospheric pollutants is comparatively low throughout most of Alaska; consequently, modifications of the original IEC design were needed. The most notable modification was conversion from a single-stage mixed-bed column to a two

Atmospheric Nitrogen Deposition in the Western United States: Sources, Sinks and Changes over Time

Science.gov (United States)

Anderson, Sarah Marie

Anthropogenic activities have greatly modified the way nitrogen moves through the atmosphere and terrestrial and aquatic environments. Excess reactive nitrogen generated through fossil fuel combustion, industrial fixation, and intensification of agriculture is not confined to anthropogenic systems but leaks into natural ecosystems with consequences including acidification, eutrophication, and biodiversity loss. A better understanding of where excess nitrogen originates and how that changes over time is crucial to identifying when, where, and to what degree environmental impacts occur. A major route into ecosystems for excess nitrogen is through atmospheric deposition. Excess nitrogen is emitted to the atmosphere where it can be transported great distances before being deposited back to the Earth's surface. Analyzing the composition of atmospheric nitrogen deposition and biological indicators that reflect deposition can provide insight into the emission sources as well as processes and atmospheric chemistry that occur during transport and what drives variation in these sources and processes. Chapter 1 provides a review and proof of concept of lichens to act as biological indicators and how their elemental and stable isotope composition can elucidate variation in amounts and emission sources of nitrogen over space and time. Information on amounts and emission sources of nitrogen deposition helps inform natural resources and land management decisions by helping to identify potentially impacted areas and causes of those impacts. Chapter 2 demonstrates that herbaria lichen specimens and field lichen samples reflect historical changes in atmospheric nitrogen deposition from urban and agricultural sources across the western United States. Nitrogen deposition increases throughout most of the 20 th century because of multiple types of emission sources until the implementation of the Clean Air Act Amendments of 1990 eventually decrease nitrogen deposition around the turn of

Study of particulate matter from Primary/Secondary Marine Aerosol and anthropogenic sources collected by a self-made passive sampler for the evaluation of the dry deposition impact on built heritage.

Science.gov (United States)

Morillas, Héctor; Maguregui, Maite; García-Florentino, Cristina; Marcaida, Iker; Madariaga, Juan Manuel

2016-04-15

Dry deposition is one of the most dangerous processes that can take place in the environment where the compounds that are suspended in the atmosphere can react directly on different surrounding materials, promoting decay processes. Usually this process is related with industrial/urban fog and/or marine aerosol in the coastal areas. Particularly, marine aerosol transports different types of salts which can be deposited on building materials and by dry deposition promotes different decay pathways. A new analytical methodology based on the combined use of Raman Spectroscopy and SEM-EDS (point-by-point and imaging) was applied. For that purpose, firstly evaporated seawater (presence of Primary Marine Aerosol (PMA)) was analyzed. After that, using a self-made passive sampler (SMPS), different suspended particles coming from marine aerosol (transformed particles in the atmosphere (Secondary Marine Aerosol (SMA)) and metallic airborne particulate matter coming from anthropogenic sources, were analyzed. Finally in order to observe if SMA and metallic particles identified in the SMPS can be deposited on a building, sandstone samples from La Galea Fortress (Getxo, north of Spain) located in front of the sea and in the place where the passive sampler was mounted were analyzed. Copyright © 2016 Elsevier B.V. All rights reserved.

Atmospheric deposition exposes Qinling pandas to toxic pollutants.

Science.gov (United States)

Chen, Yi-Ping; Zheng, Ying-Juan; Liu, Qiang; Song, Yi; An, Zhi-Sheng; Ma, Qing-Yi; Ellison, Aaron M

2017-03-01

The giant panda (Ailuropoda melanoleuca) is one of the most endangered animals in the world, and it is recognized worldwide as a symbol for conservation. A previous study showed that wild and captive pandas, especially those of the Qinling subspecies, were exposed to toxicants in their diet of bamboo; the ultimate origin of these toxicants is unknown. Here we show that atmospheric deposition is the most likely origin of heavy metals and persistent organic pollutants (POPs) in the diets of captive and wild Qinling pandas. Average atmospheric deposition was 199, 115, and 49 g·m -2 ·yr -1 in the center of Xi'an City, at China's Shaanxi Wild Animal Research Center (SWARC), and at Foping National Nature Reserve (FNNR), respectively. Atmospheric deposition of heavy metals (As, Cd, Cr, Pb, Hg, Co, Cu, Zn, Mn, and Ni) and POPs was highest at Xi'an City, intermediate at SWARC, and lowest at FNNR. Soil concentrations of the aforementioned heavy metals other than As and Zn also were significantly higher at SWARC than at FNNR. Efforts to conserve Qinling pandas may be compromised by air pollution attendant to China's economic development. Improvement of air quality and reductions of toxic emissions are urgently required to protect China's iconic species. © 2017 by the Ecological Society of America.

Gaseous Oxidized Mercury Dry Deposition Measurements in the Southwestern USA: A Comparison between Texas, Eastern Oklahoma, and the Four Corners Area

Directory of Open Access Journals (Sweden)

Mark E. Sather

2014-01-01

Full Text Available Gaseous oxidized mercury (GOM dry deposition measurements using aerodynamic surrogate surface passive samplers were collected in central and eastern Texas and eastern Oklahoma, from September 2011 to September 2012. The purpose of this study was to provide an initial characterization of the magnitude and spatial extent of ambient GOM dry deposition in central and eastern Texas for a 12-month period which contained statistically average annual results for precipitation totals, temperature, and wind speed. The research objective was to investigate GOM dry deposition in areas of Texas impacted by emissions from coal-fired utility boilers and compare it with GOM dry deposition measurements previously observed in eastern Oklahoma and the Four Corners area. Annual GOM dry deposition rate estimates were relatively low in Texas, ranging from 0.1 to 0.3 ng/m2h at the four Texas monitoring sites, similar to the 0.2 ng/m2h annual GOM dry deposition rate estimate recorded at the eastern Oklahoma monitoring site. The Texas and eastern Oklahoma annual GOM dry deposition rate estimates were at least four times lower than the highest annual GOM dry deposition rate estimate previously measured in the more arid bordering western states of New Mexico and Colorado in the Four Corners area.

Modeling the global atmospheric transport and deposition of mercury to the Great Lakes

Directory of Open Access Journals (Sweden)

Mark D. Cohen

2016-07-01

Full Text Available Abstract Mercury contamination in the Great Lakes continues to have important public health and wildlife ecotoxicology impacts, and atmospheric deposition is a significant ongoing loading pathway. The objective of this study was to estimate the amount and source-attribution for atmospheric mercury deposition to each lake, information needed to prioritize amelioration efforts. A new global, Eulerian version of the HYSPLIT-Hg model was used to simulate the 2005 global atmospheric transport and deposition of mercury to the Great Lakes. In addition to the base case, 10 alternative model configurations were used to examine sensitivity to uncertainties in atmospheric mercury chemistry and surface exchange. A novel atmospheric lifetime analysis was used to characterize fate and transport processes within the model. Model-estimated wet deposition and atmospheric concentrations of gaseous elemental mercury (Hg(0 were generally within ∼10% of measurements in the Great Lakes region. The model overestimated non-Hg(0 concentrations by a factor of 2–3, similar to other modeling studies. Potential reasons for this disagreement include model inaccuracies, differences in atmospheric Hg fractions being compared, and the measurements being biased low. Lake Erie, downwind of significant local/regional emissions sources, was estimated by the model to be the most impacted by direct anthropogenic emissions (58% of the base case total deposition, while Lake Superior, with the fewest upwind local/regional sources, was the least impacted (27%. The U.S. was the largest national contributor, followed by China, contributing 25% and 6%, respectively, on average, for the Great Lakes. The contribution of U.S. direct anthropogenic emissions to total mercury deposition varied between 46% for the base case (with a range of 24–51% over all model configurations for Lake Erie and 11% (range 6–13% for Lake Superior. These results illustrate the importance of atmospheric

Development of a distributed air pollutant dry deposition modeling framework

International Nuclear Information System (INIS)

Hirabayashi, Satoshi; Kroll, Charles N.; Nowak, David J.

2012-01-01

A distributed air pollutant dry deposition modeling system was developed with a geographic information system (GIS) to enhance the functionality of i-Tree Eco (i-Tree, 2011). With the developed system, temperature, leaf area index (LAI) and air pollutant concentration in a spatially distributed form can be estimated, and based on these and other input variables, dry deposition of carbon monoxide (CO), nitrogen dioxide (NO 2 ), sulfur dioxide (SO 2 ), and particulate matter less than 10 microns (PM10) to trees can be spatially quantified. Employing nationally available road network, traffic volume, air pollutant emission/measurement and meteorological data, the developed system provides a framework for the U.S. city managers to identify spatial patterns of urban forest and locate potential areas for future urban forest planting and protection to improve air quality. To exhibit the usability of the framework, a case study was performed for July and August of 2005 in Baltimore, MD. - Highlights: ► A distributed air pollutant dry deposition modeling system was developed. ► The developed system enhances the functionality of i-Tree Eco. ► The developed system employs nationally available input datasets. ► The developed system is transferable to any U.S. city. ► Future planting and protection spots were visually identified in a case study. - Employing nationally available datasets and a GIS, this study will provide urban forest managers in U.S. cities a framework to quantify and visualize urban forest structure and its air pollution removal effect.

Dry deposition of particulate Cs-134 to several leafy vegetable species and comparison to deposition of gaseous radioiodine

International Nuclear Information System (INIS)

Tschiersch, J.; Shinonaga, T.; Heuberger, H.

2004-01-01

The height of the dry deposition of particulate radionuclides to leafy vegetable is quite uncertain because of the different habit, surface texture and leaf uptake of the different species. There is no comparative data on the deposition to various species, but leafy vegetables are taken as reference plants for the estimation of the height of contamination of vegetable foods after a nuclear accident. Therefore new chamber experiments were performed to determine under homogeneous and controlled conditions the dry deposition of particulate radio-caesium on mature leafy vegetable. The simultaneous exposition of endive, head lettuce, red oak leaf lettuce and spinach (spring leafy vegetable) rsp. curly kale, white cabbage and spinach (summer leafy vegetable) was arranged. The sample collective of each species was such large that for the expected variation of the results a statistically firm analysis was possible. For spring vegetable, there was no significant difference observed in deposition of 134 Cs between spinach and leaf lettuce, about twice the amount was deposited on both species as on endive and 3 times as on head lettuce. All summer vegetables showed differences in deposition for Caesium, the deposition to curly kale was highest, about twice that on spinach and 35 times (80 times) that on white cabbage. The normalized deposition velocity could be estimated, in average it was about 8 times lower for 134 Cs than for gaseous elemental 131 I. The influence of the particle size on the deposition velocity was small in the considered size range of 0.58-1.1μm (AMAD) of the monodisperse aerosol. Washing could reduce the contamination by about 45% for 134 Cs. (author)

Human health risk assessment of lead pollution in atmospheric deposition in Baoshan District, Shanghai.

Science.gov (United States)

Chen, Yuanyuan; Wang, Jun; Shi, Guitao; Sun, Xiaojing; Chen, Zhenlou; Xu, Shiyuan

2011-12-01

The lead (Pb) content in atmospheric deposition was determined at 42 sampling sites in Baoshan District of Shanghai, China. Based on exposure and dose-response assessments, the health risk caused by Pb exposure in atmospheric deposition was investigated. The results indicated that Pb was significantly accumulated in atmospheric deposition. The spatial distribution of Pb was mapped by geostatistical analysis, and the results showed that pollution hotspots were present at traffic and industrial zones. Ingestion was the main route of Pb exposure in both adults and children. For children the risk value was above 1, whereas it was below 1 for the adult group. Therefore, children belong to the high-risk group for Pb exposure from atmospheric deposition in the observed area of Shanghai, China.

Contribution of Asian dust to atmospheric deposition of radioactive cesium (137Cs)

International Nuclear Information System (INIS)

Fukuyama, Taijiro; Fujiwara, Hideshi

2008-01-01

Both Asian dust (kosa) transported from the East Asian continent and locally suspended dust near monitoring sites contribute to the observed atmospheric deposition of 137 Cs in Japan. To estimate the relative contribution of these dust phenomena to the total 137 Cs deposition, we monitored weekly deposition of mineral particles and 137 Cs in spring. Deposition of 137 Cs from a single Asian dust event was 62.3 mBq m -2 and accounted for 67% of the total 137 Cs deposition during the entire monitoring period. Furthermore, we found high 137 Cs specific activity in the Asian dust deposition sample. Although local dust events contributed to 137 Cs deposition, their contribution was considerably smaller than that of Asian dust. We conclude that the primary source of atmospheric 137 Cs in Japan is dust transported from the East Asian continent

Measurement of forest condition and response along the Pennsylvania atmospheric deposition gradent

Science.gov (United States)

D.D. David; J.M. Skelly; J.A. Lynch; L.H. McCormick; B.L. Nash; M. Simini; E.A. Cameron; J.R. McClenahen; R.P. Long

1991-01-01

Research in the oak-hickory forest of northcentral Pennsylvania is being conducted to detect anomalies in forest condition that may be due to atmospheric deposition, with the intent that such anomalies will be further studied to determine the role, if any, of atmospheric deposition. This paper presents the status of research along a 160-km gradient of sulfate/nitrate...

Assessment of nitrogen as an atmosphere for dry storage of spent LWR fuel

International Nuclear Information System (INIS)

Gilbert, E.R.; Knox, C.A.; White, G.D.

1985-09-01

Interim dry storage of spent light-water reactor (LWR) fuel is being developed as a licensed technology in the United States. Because it is anticipated that license agreements will specify dry storage atmospheres, the behavior of spent LWR fuel in a nitrogen atmosphere during dry storage was investigated. In particular, the thermodynamics of reaction of nitrogen compounds (expected to form in the cover gas during dry storage) and residual impurities (such as moisture and oxygen) with Zircaloy cladding and with spent fuel at sites of cladding breaches were examined. The kinetics of reaction were not considered it was assumed that the 20 to 40 years of interim dry storage would be sufficient for reactions to proceed to completion. The primary thermodynamics reactants were found to be NO 2 , N 2 O, H 2 O 2 , and O 2 . The evaluation revealed that the limited inventories of these reactants produced by the source terms in hermetically sealed dry storage systems would be too low to cause significant spent fuel degradation. Furthermore, the oxidation of spent fuel to degrading O/U ratios is unlikely because the oxidation potential in moist nitrogen limits O/U ratios to values less than UO/sub 2.006/ (the equilibrium stoichiometric form in equilibrium with moist nitrogen). Tests were performed with bare spent UO 2 fuel and nonirradiated UO 2 pellets (with no Zircaloy cladding) in a nitrogen atmosphere containing moisture concentrations greater than encountered under dry storage conditions. These tests were performed for at least 1100 h at temperatures as high as 380 0 C, where oxidation reactions proceed in a matter of minutes. No visible degradation was detected, and weight changes were negligible

Deposition of radionuclides and stable elements in Tokai-mura

Energy Technology Data Exchange (ETDEWEB)

Ueno, Takashi; Amano, Hikaru [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment

2003-03-01

This report presents the data of deposition of radionuclides (Sep. 1993-March 2001) and stable elements (Sep. 1993-Oct. 1995) in Tokai-mura. To evaluate the migration of radionuclides and stable elements from the atmosphere to the ground surface, atmospheric deposition samples were collected from Sep. 1993 to March 2001 with three basins (distance to grand surface were 1.5 m, 4 m, 10 m) set up in the enclosure of JAERI in Tokai-mura, Ibaraki-ken, Japan. Monthly samples were evaporated to dryness to obtain residual samples and measured with a well type Ge detector for {sup 7}Be, {sup 40}K, {sup 137}Cs and {sup 210}Pb. According to the analysis of radioactivity, clear seasonal variations with spring peaks of deposition weight (dry) and deposition amounts of all objective radionuclides were found. Correlation analysis of deposition data also showed that these radionuclides can be divided into two groups. A part of dried sample was irradiated to reactor neutrons at JRR-4 for determination of stable element's deposition. (author)

Atmospheric wet deposition of mercury in North America

Energy Technology Data Exchange (ETDEWEB)

Sweet, C.W.; Prestbo, E.; Brunette, B.

1999-07-01

Currently, 39 states in the US and 5 Canadian provinces have issued advisories about the dangers of eating mercury-contaminated fish taken from waters within their boundaries. The problem is most severe in the Great Lakes region, the Northeast US states, the Canadian maritime provinces, and in south Florida where many lakes and streams contain fish with concentrations of 1 ppm or higher. For many rural and remote locations, atmospheric deposition is the primary source of mercury. In 1995, the National Atmospheric Deposition Program (NADP) initiated a program to monitor total mercury and methylmercury (MMHg) in wet deposition (rain and snow) in North America. In this program, the Mercury Deposition Network (MDN), individual monitoring sites are funded and operated by a variety of local, state, and federal agencies. However, sampling and analysis are coordinated through a central laboratory so that all of the samples are collected and analyzed using the same protocols. Weekly wet-only precipitation samples are collected using an all-glass sampling train and special handling techniques. Analysis is by cold vapor atomic fluorescence spectrometry using USEPA Method 1631 for total mercury. Nearly 40 MDN sites are in operation in 1999. Most of the sites are in the eastern US and Canada. During 1996 and 1997, the volume-weighted mean concentration of total mercury in precipitation collected at 22 sites ranged from 6.0 to 18.9 ng/L. Annual deposition varied between 2.1 and 25.3 {micro} g/m{sup 2}. The average weekly wet deposition of total mercury is more than three times higher in the summer (June-August) than in the winter (December-February). This increase is due to both higher amounts of precipitation and higher concentrations of mercury in precipitation during the summer. The highest values for mercury concentration in precipitation and wet deposition of mercury were measured in the southeastern US.

Oceanic Emissions and Atmospheric Depositions of Volatile Organic Compounds

Science.gov (United States)

Yang, M.; Blomquist, B.; Beale, R.; Nightingale, P. D.; Liss, P. S.

2015-12-01

Atmospheric volatile organic compounds (VOCs) affect the tropospheric oxidative capacity due to their ubiquitous abundance and relatively high reactivity towards the hydroxyal radical. Over the ocean and away from terrestrial emission sources, oxygenated volatile organic compounds (OVOCs) make up a large fraction of VOCs as airmasses age and become more oxidized. In addition to being produced or destroyed in the marine atmosphere, OVOCs can also be emitted from or deposited to the surface ocean. Here we first present direct air-sea flux measurements of three of the most abundant OVOCs - methanol, acetone, and acetaldehyde, by the eddy covariance technique from two cruises in the Atlantic: the Atlantic Meridional Transect in 2012 and the High Wind Gas Exchange Study in 2013. The OVOC mixing ratios were quantified by a high resolution proton-reaction-transfer mass spectrometer with isotopically labeled standards and their air-sea (net) fluxes were derived from the eddy covariance technique. Net methanol flux was consistently from the atmosphere to the surface ocean, while acetone varied from supersaturation (emission) in the subtropics to undersaturation (deposition) in the higher latitudes of the North Atlantic. The net air-sea flux of acetaldehyde is near zero through out the Atlantic despite the apparent supersaturation of this compound in the surface ocean. Knowing the dissolved concentrations and in situ production rates of these compounds in seawater, we then estimate their bulk atmospheric depositions and oceanic emissions. Lastly, we summarize the state of knowledge on the air-sea transport of a number of organic gasses, and postulate the magnitude and environmental impact of total organic carbon transfer between the ocean and the atmosphere.

Standard test method for determining atmospheric chloride deposition rate by wet candle method

CERN Document Server

American Society for Testing and Materials. Philadelphia

2002-01-01

1.1 This test method covers a wet candle device and its use in measuring atmospheric chloride deposition (amount of chloride salts deposited from the atmosphere on a given area per unit time). 1.2 Data on atmospheric chloride deposition can be useful in classifying the corrosivity of a specific area, such as an atmospheric test site. Caution must be exercised, however, to take into consideration the season because airborne chlorides vary widely between seasons. 1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

Recent Advances in Atmospheric Vapor-Phase Deposition of Transparent and Conductive Zinc Oxide

NARCIS (Netherlands)

Illiberi, A.; Poodt, P.; Roozeboom, F.

2014-01-01

The industrial need for high-throughput and low-cost ZnO deposition processes has triggered the development of atmospheric vapor-phase deposition techniques which can be easily applied to continuous, in-line manufacturing. While atmospheric CVD is a mature technology, new processes for the growth of

Seasonal phosphatase activity in three characteristic soils of the English uplands polluted by long-term atmospheric nitrogen deposition

International Nuclear Information System (INIS)

Turner, B.L.; Baxter, Robert; Whitton, B.A.

2002-01-01

High soil phosphatase activities confirm strong biological phosphorus limitations due to nitrogen deposition. - Phosphomonoesterase activities were determined monthly during a seasonal cycle in three characteristic soil types of the English uplands that have been subject to long-term atmospheric nitrogen deposition. Activities (μmol para-nitrophenol g -1 soil dry wt. h -1 ) ranged between 83.9 and 307 in a blanket peat (total carbon 318 mg g -1 , pH 3.9), 45.2-86.4 in an acid organic grassland soil (total carbon 354 mg g -1 , pH 3.7) and 10.4-21.1 in a calcareous grassland soil (total carbon 140 mg g -1 , pH 7.3). These are amongst the highest reported soil phosphomonoesterase activities and confirm the strong biological phosphorus limitation in this environment

Organic nitrogen and carbon in atmospheric dry and wet depositions in the southern East China Sea: its implication for new production in coastal region

Science.gov (United States)

Chen, H. Y.; Yeh, J. X.; Lin, C. T.

2016-02-01

We collected 11 sets of size-segregated particulate aerosol (include coarse and fine particles) and 53 rain samples from January to December 2014 at a coastal city (Keelung) on the southern East China Sea. Here we present measurements of water-soluble inorganic/organic nitrogen and carbon (WSIN/WSON and WSIC/WSOC, respectively) in aerosol samples and dissolved inorganic/organic nitrogen and carbon (DIN/DON and DIC/DOC, respectively) in rain samples. In addition, 4-d back trajectories of air masses arriving daily at the sampling site were calculated to determine the potential aerosol source regions. The concentrations of water-soluble species in particulate aerosols were relatively high in March (WSON: 223±48 nmol m-3; WSOC: 203±51 nmol m-3) and dissolved species in rain samples were high in December (DON: 157±69 μM; DOC: 294±168 μM), which occur frequently during the spring and winter. The monsoon system of East Asia play a key role on the atmospheric composition of nitrogen and carbon, with higher loadings in northerly (winter to spring) than southerly (summer to autumn) monsoon periods, owing to strong emissions from the East Asian continent. Our results indicate that biomass burning and dust events yielded the largest concentrations of ON and OC not only on particulate aerosols but also in precipitations. For aerosols, the amounts of WSON and WSOC accounted for 42±8% and 80±7% of the water-soluble total nitrogen (WSTN) and carbon (WSTC), respectively. Additionally, the concentrations of DON and DOC accounted for 40±5% and 75±3% of total dissolved nitrogen (TDN) and carbon (TDC), respectively, for precipitations. By using dry and wet deposition flux estimations, we estimated that the fluxes of WSTN/TDN and WSTC/TDC were 47.1±24.4 / 266±20 mmol m-2 yr-1 and 23±9 / 153±3 mmol m-2 yr-1, respectively. These results suggest that atmospheric deposition contributed approximately 25-34% of the annual biological new production in the southern East China Sea.

Evaluating Ammonia Deposition Rates for Deciduous Forest using Measurements and Modelling

DEFF Research Database (Denmark)

Hansen, Kristina; Geels, Camilla; Hertel, Ole

). However, there are relatively few datasets of atmospheric NH3 fluxes available for forests which can contribute verifying model results. The atmospheric dry deposition of NH3 for the beech (Fagus sylvatica) forest, Lille Bøgeskov, in Sorø, Denmark, is investigated using the high resolution...... these impacts, quantifying the magnitude of the NH3 flux in the biosphere atmosphere system is essential. Model simulations using the Danish Ammonia Modelling System (DAMOS) have recently indicated that particular forest ecosystems are exposed to critical load exceedances of N (Geels et al., not yet submitted......-agricultural areas (Skjøth et al. 2011, ACPD). New atmospheric NH3 flux measurements for Lille Bøgeskov have been conducted throughout 2011 and these data are presented and discussed in relation to the 2010 data of atmospheric NH3. Future studies aim to improve the description of dry deposition of NH3 for vegetative...

Atmospheric deposition of 137Cs between 1994 and 2002 at Cienfuegos, Cuba

International Nuclear Information System (INIS)

Alonso-Hernandez, C.M.; Cartas-Aguila, H.; Diaz-Asencio, M.; Munoz-Caravaca, A.; Martin-Perez, J.; Sibello-Hernandez, R.

2006-01-01

Levels of 137 Cs in total atmospheric deposition have been measured in the Cienfuegos region (Cuba) between 1994 and 2002. Samples were collected every three months, evaporated to dryness to obtain residual samples, and measured by gamma spectrometry. The 137 Cs mean concentration in total deposition was 0.24 Bq m -2 and data ranged between -2 . Precipitation rates and raintime have proved to be the most important factors controlling the concentration and depositional flux of 137 Cs in the atmosphere over Cienfuegos, showing a high correlation coefficient (R = 0.93)

Atmospheric bulk deposition of polycyclic aromatic hydrocarbons in Shanghai: Temporal and spatial variation, and global comparison

International Nuclear Information System (INIS)

Feng, Daolun; Liu, Ying; Gao, Yi; Zhou, Jinxing; Zheng, Lirong; Qiao, Gang; Ma, Liming; Lin, Zhifen; Grathwohl, Peter

2017-01-01

Atmospheric deposition leads to accumulation of atmospheric polycyclic aromatic hydrocarbons (PAHs) on urban surfaces and topsoils. To capture the inherent variability of atmospheric deposition of PAHs in Shanghai's urban agglomeration, 85 atmospheric bulk deposition samples and 7 surface soil samples were collected from seven sampling locations during 2012–2014. Total fluxes of 17 PAHs were 587-32,300 ng m −2 day −1 , with a geometric mean of 2600 ng m −2 day −1 . The deposition fluxes were categorized as moderate to high on a global scale. Phenanthrene, fluoranthene and pyrene were major contributors. The spatial distribution of deposition fluxes revealed the influence of urbanization/industrialization and the relevance of local emissions. Meteorological conditions and more heating demand in cold season lead to a significant increase of deposition rates. Atmospheric deposition is the principal pathway of PAHs input to topsoils and the annual deposition load in Shanghai amounts to ∼4.5 tons (0.7 kg km −2 ) with a range of 2.5–10 tons (0.4–1.6 kg km −2 ). - Highlights: • PAH deposition flux in Shanghai is categorized as moderate to high on global scale. • Their spatial distribution reveals the influence of urbanization/industrialization. • Atmospheric deposition is the principal pathway of PAHs input to local topsoils. • Other pathways have to be considered for PAH input in urban soil. - Atmospheric deposition of PAHs revealed the influence of urbanization and industrialization and the relevance of local emissions on Shanghai topsoils.

Accounting for Field-Scale Dry Deposition in Backward Lagrangian Stochastic Dispersion Modelling of NH3 Emissions

Directory of Open Access Journals (Sweden)

Christoph Häni

2018-04-01

Full Text Available A controlled ammonia (NH3 release experiment was performed at a grassland site. The aim was to quantify the effect of dry deposition between the source and the receptors (NH3 measurement locations on emission rate estimates by means of inverse dispersion modelling. NH3 was released for three hours at a constant rate of Q = 6.29 mg s−1 from a grid of 36 orifices spread over an area of 250 m2. The increase in line-integrated NH3 concentration was measured with open-path optical miniDOAS devices at different locations downwind of the artificial source. Using a backward Lagrangian stochastic (bLS dispersion model (bLSmodelR, the fraction of the modelled release rate to the emitted NH3 ( Q bLS / Q was calculated from the measurements of the individual instruments. Q bLS / Q was found to be systematically lower than 1, on average between 0.69 and 0.91, depending on the location of the receptor. We hypothesized that NH3 dry deposition to grass and soil surfaces was the main factor responsible for the observed depletion of NH3 between source and receptor. A dry deposition algorithm based on a deposition velocity approach was included in the bLS modelling. Model deposition velocities were evaluated from a ‘big-leaf’ canopy resistance analogy. Canopy resistances (generally termed R c that provided Q bLS / Q = 1 ranged from 75 to 290 s m−1, showing that surface removal of NH3 by dry deposition can plausibly explain the original underestimation of Q bLS / Q . The inclusion of a dry deposition process in dispersion modelling is crucial for emission estimates, which are based on concentration measurements of depositing tracers downwind of homogeneous area sources or heterogeneously-distributed hot spots, such as, e.g., urine patches on pastures in the case of NH3.

Consolidation and atmospheric drying of fine oil sand tailings : Comparison of blind simulations and field scale results

NARCIS (Netherlands)

Vardon, P.J.; Yao, Y.; van Paassen, L.A.; van Tol, A.F.; Sego, D.C.; Wilson, G.W.; Beier, N.A.

2016-01-01

This paper presents a comparison between blind predictions of field tests of atmospheric drying of mature fine tailings (MFT) presented in IOSTC 2014 and field results. The numerical simulation of the consolidation and atmospheric drying of selfweight consolidating fine material is challenging and

The measurement of dry deposition and surface runoff to quantify urban road pollution in Taipei, Taiwan.

Science.gov (United States)

Wang, Yunn-Jinn; Chen, Chi-Feng; Lin, Jen-Yang

2013-10-16

Pollutants deposited on road surfaces and distributed in the environment are a source of nonpoint pollution. Field data are traditionally hard to collect from roads because of constant traffic. In this study, in cooperation with the traffic administration, the dry deposition on and road runoff from urban roads was measured in Taipei City and New Taipei City, Taiwan. The results showed that the dry deposition is 2.01-5.14 g/m(2) · day and 78-87% of these solids are in the 75-300 µm size range. The heavy metals in the dry deposited particles are mainly Fe, Zn, and Na, with average concentrations of 34,978, 1,519 and 1,502 ppm, respectively. Elevated express roads show the highest heavy metal concentrations. Not only the number of vehicles, but also the speed of the traffic should be considered as factors that influence road pollution, as high speeds may accelerate vehicle wear and deposit more heavy metals on road surfaces. In addition to dry deposition, the runoff and water quality was analyzed every five minutes during the first two hours of storm events to capture the properties of the first flush road runoff. The sample mean concentration (SMC) from three roads demonstrated that the first flush runoff had a high pollution content, notably for suspended solid (SS), chemical oxygen demand (COD), oil and grease, Pb, and Zn. Regular sweeping and onsite water treatment facilities are suggested to minimize the pollution from urban roads.

Source, flux and balance of atmospheric deposition of metals at Ile-de-France; Source, flux et bilan des retombees atmospheriques de metaux en Ile de France

Energy Technology Data Exchange (ETDEWEB)

Azimi, S

2004-07-15

The urban atmosphere is submitted to large inputs of anthropogenic contaminants arising from both stationary (power plants, industries, etc.) and mobile (road traffic) sources. These small particles may be transported over long distances and affect ecosystems. Significant dry and wet atmospheric deposition also occurs locally and contributes to the contamination of urban runoff. The aim of this study is to compare heavy metal and hydrocarbon atmospheric deposition fluxes to other input ways on agricultural and urban areas to assess their importance. Moreover, a source investigation has been done to identify the main origins of these pollutants. Before the quantification of pollutant fluxes, a comparison of several sampling procedures was performed. As a result, the sampling of total atmospheric deposition is not affected by the funnel material (Teflon and polyethylene) or by the sampling duration (7 and 28 days). However, the rinsing step of the funnel walls showed a higher relative importance during short sampling periods. The relative amount contained in these solutions reached 24 to 40 % of the total flux during weekly sampling periods and 8 to 18 % during monthly sampling periods, whatever the element considered. The temporal evolution of atmospheric deposition showed no seasonal influence on flux variations during the 2001-2002 period. Considering an 8-year period behaviour, between 1994 and 2002, a significant decrease of the deposition fluxes of Cd, Cu, Pb and Zn occurred at the Creteil site which is placed in an industrialized area of the Paris suburb. The decreasing factor reached 16, 2.5, 4 and 7.5 for these elements respectively. At the Ile-de-France scale, the deposition flux levels on urban and semi-urban areas were of the same order of magnitude (?20 tonnes per year for Ba, Cu, Pb and Sr). Since semi-urban surface area is four times higher than urban ones, the important influence of anthropogenic activities on atmospheric deposition of urban areas is

Methods, quality assurance, and data for assessing atmospheric deposition of pesticides in the Central Valley of California

Science.gov (United States)

Zamora, Celia; Majewski, Michael S.; Foreman, William T.

2013-01-01

The U.S. Geological Survey monitored atmospheric deposition of pesticides in the Central Valley of California during two studies in 2001 and 2002–04. The 2001 study sampled wet deposition (rain) and storm-drain runoff in the Modesto, California, area during the orchard dormant-spray season to examine the contribution of pesticide concentrations to storm runoff from rainfall. In the 2002–04 study, the number and extent of collection sites in the Central Valley were increased to determine the areal distribution of organophosphate insecticides and other pesticides, and also five more sample types were collected. These were dry deposition, bulk deposition, and three sample types collected from a soil box: aqueous phase in runoff, suspended sediment in runoff, and surficial-soil samples. This report provides concentration data and describes methods and quality assurance of sample collection and laboratory analysis for pesticide compounds in all samples collected from 16 sites. Each sample was analyzed for 41 currently used pesticides and 23 pesticide degradates, including oxygen analogs (oxons) of 9 organophosphate insecticides. Analytical results are presented by sample type and study period. The median concentrations of both chloryprifos and diazinon sampled at four urban (0.067 micrograms per liter [μg/L] and 0.515 μg/L, respectively) and four agricultural sites (0.079 μg/L and 0.583 μg/L, respectively) during a January 2001 storm event in and around Modesto, Calif., were nearly identical, indicating that the overall atmospheric burden in the region appeared to be fairly similar during the sampling event. Comparisons of median concentrations in the rainfall to those in the McHenry storm-drain runoff showed that, for some compounds, rainfall contributed a substantial percentage of the concentration in the runoff; for other compounds, the concentrations in rainfall were much greater than in the runoff. For example, diazinon concentrations in rainfall were about

Rapid Deposition of Oxidized Biogenic Compounds to a Temperate Forest

Science.gov (United States)

Nguyen, Tran B.; Crounse, John D.; Teng, Alex P.; St. Clair, Jason M.; Paulot, Fabien; Wolfe, Glenn M.; Wennberg, Paul O.

2015-01-01

We report fluxes and dry deposition velocities for 16 atmospheric compounds above a southeastern United States forest, including: hydrogen peroxide (H2O2), nitric acid (HNO3), hydrogen cyanide (HCN), hydroxymethyl hydroperoxide, peroxyacetic acid, organic hydroxy nitrates, and other multifunctional species derived from the oxidation of isoprene and monoterpenes. The data suggest that dry deposition is the dominant daytime sink for small, saturated oxygenates. Greater than 6 wt %C emitted as isoprene by the forest was returned by dry deposition of its oxidized products. Peroxides account for a large fraction of the oxidant flux, possibly eclipsing ozone in more pristine regions. The measured organic nitrates comprise a sizable portion (15%) of the oxidized nitrogen input into the canopy, with HNO3 making up the balance. We observe that water-soluble compounds (e.g., strong acids and hydroperoxides) deposit with low surface resistance whereas compounds with moderate solubility (e.g., organic nitrates and hydroxycarbonyls) or poor solubility (e.g., HCN) exhibited reduced uptake at the surface of plants. To first order, the relative deposition velocities of water-soluble compounds are constrained by their molecular diffusivity. From resistance modeling, we infer a substantial emission flux of formic acid at the canopy level (approx. 1 nmol m(exp.-2)·s(exp.-1)). GEOS-Chem, awidely used atmospheric chemical transport model, currently underestimates dry deposition for most molecules studied in this work. Reconciling GEOS-Chem deposition velocities with observations resulted in up to a 45% decrease in the simulated surface concentration of trace gases.

Assessment of Global Mercury Deposition through Litterfall.

Science.gov (United States)

Wang, Xun; Bao, Zhengduo; Lin, Che-Jen; Yuan, Wei; Feng, Xinbin

2016-08-16

There is a large uncertainty in the estimate of global dry deposition of atmospheric mercury (Hg). Hg deposition through litterfall represents an important input to terrestrial forest ecosystems via cumulative uptake of atmospheric Hg (most Hg(0)) to foliage. In this study, we estimate the quantity of global Hg deposition through litterfall using statistical modeling (Monte Carlo simulation) of published data sets of litterfall biomass production, tree density, and Hg concentration in litter samples. On the basis of the model results, the global annual Hg deposition through litterfall is estimated to be 1180 ± 710 Mg yr(-1), more than two times greater than the estimate by GEOS-Chem. Spatial distribution of Hg deposition through litterfall suggests that deposition flux decreases spatially from tropical to temperate and boreal regions. Approximately 70% of global Hg(0) dry deposition occurs in the tropical and subtropical regions. A major source of uncertainty in this study is the heterogeneous geospatial distribution of available data. More observational data in regions (Southeast Asia, Africa, and South America) where few data sets exist will greatly improve the accuracy of the current estimate. Given that the quantity of global Hg deposition via litterfall is typically 2-6 times higher than Hg(0) evasion from forest floor, global forest ecosystems represent a strong Hg(0) sink.

Atmospheric bulk deposition of polycyclic aromatic hydrocarbons in Shanghai: Temporal and spatial variation, and global comparison.

Science.gov (United States)

Feng, Daolun; Liu, Ying; Gao, Yi; Zhou, Jinxing; Zheng, Lirong; Qiao, Gang; Ma, Liming; Lin, Zhifen; Grathwohl, Peter

2017-11-01

Atmospheric deposition leads to accumulation of atmospheric polycyclic aromatic hydrocarbons (PAHs) on urban surfaces and topsoils. To capture the inherent variability of atmospheric deposition of PAHs in Shanghai's urban agglomeration, 85 atmospheric bulk deposition samples and 7 surface soil samples were collected from seven sampling locations during 2012-2014. Total fluxes of 17 PAHs were 587-32,300 ng m -2 day -1 , with a geometric mean of 2600 ng m -2 day -1 . The deposition fluxes were categorized as moderate to high on a global scale. Phenanthrene, fluoranthene and pyrene were major contributors. The spatial distribution of deposition fluxes revealed the influence of urbanization/industrialization and the relevance of local emissions. Meteorological conditions and more heating demand in cold season lead to a significant increase of deposition rates. Atmospheric deposition is the principal pathway of PAHs input to topsoils and the annual deposition load in Shanghai amounts to ∼4.5 tons (0.7 kg km -2 ) with a range of 2.5-10 tons (0.4-1.6 kg km -2 ). Copyright © 2017 Elsevier Ltd. All rights reserved.

Atmospheric metal deposition in France: Estimation based on moss analysis. First results

International Nuclear Information System (INIS)

Galsomies, L.; Letrouit-Galinou, M.A.; Avnaim, M.; Duclaux, G.; Deschamps, C.; Savanne, D.

2000-01-01

The aim of this programme set up by University Pierre and Marie Curie-Paris VI and ADEME (French Agency for the Environment and Energy Management) is to obtain information on the atmospheric deposition of 36 elements (most being heavy metals) all over France, using 5 common mosses as bioaccumulators: Pleurozium schreberi, Hylocomium splendens, Hypnum cupressiforme, Scleropodium purum and Thuidium tamariscinum. Sampling was performed in 1996 from April to November thanks to 43 collectors. One sample of moss at least has been collected in 512 sites distributed over France, with an average density of one site each 1000 km 2 . Procedures for sampling, drying, cleaning, sorting are strictly codified based on Scandinavian guidelines. Analyses are performed according to two procedures: ICP-MS (Inductively Coupled Plasma, Mass Spectrometry) for Pb, Ni specialty and INAA (instrumental Neutron Activation Analysis for other elements. Data concerning As, Cd, Cr, Cu, Fe, Hg, Pb. Ni, V, Zn will be incorporated into the 1995-1996 European Programme 'Atmospheric Heavy Metal Deposition in Europe - estimation based on moss analysis' coordinated by the Nordic Council. The analyses are in progress, but preliminary results from Ile-de-France have been achieved for 34 elements in INAA. A preliminary study has shown that interspecies calibration could be possible for some heavy metals and that saturation effects in one species could be present when the intercalibration between species is not possible. Such a programme is made possible thanks to the financial support of the French Ministry of Environment and ADEME and with the active cooperation of several national organisations, especially the Laboratory Pierre Sue (CNRS-CEA). (author)

Carbonaceous species in atmospheric aerosols from the Krakow area (Malopolska District: carbonaceous species dry deposition analysis

Directory of Open Access Journals (Sweden)

Szramowiat Katarzyna

2016-01-01

Full Text Available Organic and elemental carbon content in PM10 was studied at three sites in Malopolska District representing the city centre (Krakow, rural/residential (Bialka and residential/industrial environments (Krakow. The PM10 samples were collected during the winter time study. The highest concentrations of carbonaceous species were observed in Skawina (36.9 μg·m-3 of OC and 9.6 μg·m-3 of EC. The lowest OC and EC concentrations were reported in Krakow (15.2 μg·m-3 and 3.9 μg·m-3, respectively. The highest concentration of carbonaceous species and the highest wind velocities in Skawina influenced the highest values of the dry deposition fluxes. Correlations between OC, EC and chemical constituents and meteorological parameters suggest that a Krakow was influenced by local emission sources and temperature inversion occurrence; b Bialka was under the influence of local emission sources and long-range transport of particles; c Skawina was impacted by local emission sources.

Detailed source term estimation of the atmospheric release for the Fukushima Daiichi Nuclear Power Station accident by coupling simulations of an atmospheric dispersion model with an improved deposition scheme and oceanic dispersion model

Energy Technology Data Exchange (ETDEWEB)

Katata, G.; Chino, M.; Kobayashi, T. [Japan Atomic Energy Agency (JAEA), Ibaraki (Japan); and others

2015-07-01

Temporal variations in the amount of radionuclides released into the atmosphere during the Fukushima Daiichi Nuclear Power Station (FNPS1) accident and their atmospheric and marine dispersion are essential to evaluate the environmental impacts and resultant radiological doses to the public. In this paper, we estimate the detailed atmospheric releases during the accident using a reverse estimation method which calculates the release rates of radionuclides by comparing measurements of air concentration of a radionuclide or its dose rate in the environment with the ones calculated by atmospheric and oceanic transport, dispersion and deposition models. The atmospheric and oceanic models used are WSPEEDI-II (Worldwide version of System for Prediction of Environmental Emergency Dose Information) and SEA-GEARN-FDM (Finite difference oceanic dispersion model), both developed by the authors. A sophisticated deposition scheme, which deals with dry and fog-water depositions, cloud condensation nuclei (CCN) activation, and subsequent wet scavenging due to mixed-phase cloud microphysics (in-cloud scavenging) for radioactive iodine gas (I{sub 2} and CH{sub 3}I) and other particles (CsI, Cs, and Te), was incorporated into WSPEEDI-II to improve the surface deposition calculations. The results revealed that the major releases of radionuclides due to the FNPS1 accident occurred in the following periods during March 2011: the afternoon of 12 March due to the wet venting and hydrogen explosion at Unit 1, midnight of 14 March when the SRV (safety relief valve) was opened three times at Unit 2, the morning and night of 15 March, and the morning of 16 March. According to the simulation results, the highest radioactive contamination areas around FNPS1 were created from 15 to 16 March by complicated interactions among rainfall, plume movements, and the temporal variation of release rates. The simulation by WSPEEDI-II using the new source term reproduced the local and regional patterns of

Three air quality studies: Great Lakes ozone formation and nitrogen dry deposition; and Tucson aerosol chemical characterization

Science.gov (United States)

Foley, Theresa

(arsenic, beryllium, cadmium, chromium, cobalt, lead, manganese, and nickel) in the southern Tucson metropolitan area. A Tucson company that uses beryllium oxide to manufacture thermally conductive ceramics has prompted strong citizen concern. This study found that the study area has good air quality with respect to PM10 and metals, with ambient concentrations meeting US Environmental Protection Agency and World Health Organization standards. Beryllium was detected only once (during a dust storm) and was ascribed to naturally-occurring beryllium in the suspended soil. The third paper (to be submitted to the Journal of Great Lakes Research) studies nitrogen dry deposition over Lake Michigan and Lake Superior. Numerous studies have shown that wet and dry deposition of nitrogen has contributed to the eutrophication of coastal waters and declining productivity of marine fisheries. Nitrogen dry deposition over the Great Lakes themselves, as opposed to the shorelines, has not been documented in the peer-reviewed literature. This paper calculates nitrogen dry deposition over Lake Michigan and Lake Superior, using aircraft measurements from the LADCO Aircraft Study, and finds that over-water, nitrogen dry deposition is a significant source of nitrogen to Lake Michigan and Lake Superior.

A seasonal nitrogen deposition budget for Rocky Mountain National Park.

Science.gov (United States)

Benedict, K B; Carrico, C M; Kreidenweis, S M; Schichtel, B; Malm, W C; Collett, J L

2013-07-01

Nitrogen deposition is a concern in many protected ecosystems around the world, yet few studies have quantified a complete reactive nitrogen deposition budget including all dry and wet, inorganic and organic compounds. Critical loads that identify the level at which nitrogen deposition negatively affects an ecosystem are often defined using incomplete reactive nitrogen budgets. Frequently only wet deposition of ammonium and nitrate are considered, despite the importance of other nitrogen deposition pathways. Recently, dry deposition pathways including particulate ammonium and nitrate and gas phase nitric acid have been added to nitrogen deposition budgets. However, other nitrogen deposition pathways, including dry deposition of ammonia and wet deposition of organic nitrogen, still are rarely included. In this study, a more complete seasonal nitrogen deposition budget was constructed based on observations during a year-long study period from November 2008 to November 2009 at a location on the east side of Rocky Mountain National Park (RMNP), Colorado, USA. Measurements included wet deposition of ammonium, nitrate, and organic nitrogen, PM2.5 (particulate matter with an aerodynamic diameter less than 2.5 microm, nitrate, and ammonium) concentrations of ammonium, nitrate, and organic nitrogen, and atmospheric gas phase concentrations of ammonia, nitric acid, and NO2. Dry deposition fluxes were determined from measured ambient concentrations and modeled deposition velocities. Total reactive nitrogen deposition by all included pathways was found to be 3.65 kg N x ha(-1) yr(-1). Monthly deposition fluxes ranged from 0.06 to 0.54 kg N x ha(-1)yr(-1), with peak deposition in the month of July and the least deposition in December. Wet deposition of ammonium and nitrate were the two largest deposition pathways, together contributing 1.97 kg N x ha(-1)yr(-1) or 54% of the total nitrogen deposition budget for this region. The next two largest deposition pathways were wet

Transport and solubility of Hetero-disperse dry deposition particulate matter subject to urban source area rainfall-runoff processes

Science.gov (United States)

Ying, G.; Sansalone, J.

2010-03-01

SummaryWith respect to hydrologic processes, the impervious pavement interface significantly alters relationships between rainfall and runoff. Commensurate with alteration of hydrologic processes the pavement also facilitates transport and solubility of dry deposition particulate matter (PM) in runoff. This study examines dry depositional flux rates, granulometric modification by runoff transport, as well as generation of total dissolved solids (TDS), alkalinity and conductivity in source area runoff resulting from PM solubility. PM is collected from a paved source area transportation corridor (I-10) in Baton Rouge, Louisiana encompassing 17 dry deposition and 8 runoff events. The mass-based granulometric particle size distribution (PSD) is measured and modeled through a cumulative gamma function, while PM surface area distributions across the PSD follow a log-normal distribution. Dry deposition flux rates are modeled as separate first-order exponential functions of previous dry hours (PDH) for PM and suspended, settleable and sediment fractions. When trans-located from dry deposition into runoff, PSDs are modified, with a d50m decreasing from 331 to 14 μm after transport and 60 min of settling. Solubility experiments as a function of pH, contact time and particle size using source area rainfall generate constitutive models to reproduce pH, alkalinity, TDS and alkalinity for historical events. Equilibrium pH, alkalinity and TDS are strongly influenced by particle size and contact times. The constitutive leaching models are combined with measured PSDs from a series of rainfall-runoff events to demonstrate that the model results replicate alkalinity and TDS in runoff from the subject watershed. Results illustrate the granulometry of dry deposition PM, modification of PSDs along the drainage pathway, and the role of PM solubility for generation of TDS, alkalinity and conductivity in urban source area rainfall-runoff.

Spatial patterns of atmospheric deposition of nitrogen and sulfur using ion-exchange resin collectors in Rocky Mountain National Park, USA

Science.gov (United States)

Clow, David W.; Roop, Heidi; Nanus, Leora; Fenn, Mark; Sexstone, Graham A.

2015-01-01

Lakes and streams in Class 1 wilderness areas in the western United States (U.S.) are at risk from atmospheric deposition of nitrogen (N) and sulfur (S), and protection of these resources is mandated under the Federal Clean Air Act and amendments. Assessment of critical loads, which are the maximum exposure to pollution an area can receive without adverse effects on sensitive ecosystems, requires accurate deposition estimates. However, deposition is difficult and expensive to measure in high-elevation wilderness, and spatial patterns in N and S deposition in these areas remain poorly quantified. In this study, ion-exchange resin (IER) collectors were used to measure dissolved inorganic N (DIN) and S deposition during June 2006–September 2007 at approximately 20 alpine/subalpine sites spanning the Continental Divide in Rocky Mountain National Park. Results indicated good agreement between deposition estimated from IER collectors and commonly used wet + dry methods during summer, but poor agreement during winter. Snowpack sampling was found to be a more accurate way of quantifying DIN and S deposition during winter. Summer DIN deposition was significantly greater on the east side of the park than on the west side (25–50%; p ≤ 0.03), consistent with transport of pollutants to the park from urban and agricultural areas to the east. Sources of atmospheric nitrate (NO3−) were examined using N isotopes. The average δ15N of NO3− from IER collectors was 3.5‰ higher during winter than during summer (p model critical loads by filling gaps in geographic coverage of deposition monitoring/modeling programs and thus may enable policy makers to better protect sensitive natural resources in Class 1 Wilderness areas.

Development of a dual-tracer real-time particle dry-deposition measurement technique for simple and complex terrain

International Nuclear Information System (INIS)

Sehmel, G.A.; Hodgson, W.H.; Campbell, J.A.

1979-01-01

Detectors are being developed and tested for measuring the airborne concentrations of lithium particles and SF 6 gas in real time. The airborne lithium detector will be used for real-time measurements of both particle dry-deposition velocities and resuspension rates. Both the lithium and SF 6 detectors will be used for measuring dry deposition in field experiments

Measured and modeled dry deposition velocities over the ESCOMPTE area

Science.gov (United States)

Michou, M.; Laville, P.; Serça, D.; Fotiadi, A.; Bouchou, P.; Peuch, V.-H.

2005-03-01

Measurements of the dry deposition velocity of ozone have been made by the eddy correlation method during ESCOMPTE (Etude sur Site pour COntraindre les Modèles de Pollution atmosphérique et de Transport d'Emissions). The strong local variability of natural ecosystems was sampled over several weeks in May, June and July 2001 for four sites with varying surface characteristics. The sites included a maize field, a Mediterranean forest, a Mediterranean shrub-land, and an almost bare soil. Measurements of nitrogen oxide deposition fluxes by the relaxed eddy correlation method have also been carried out at the same bare soil site. An evaluation of the deposition velocities computed by the surface module of the multi-scale Chemistry and Transport Model MOCAGE is presented. This module relies on a resistance approach, with a detailed treatment of the stomatal contribution to the surface resistance. Simulations at the finest model horizontal resolution (around 10 km) are compared to observations. If the seasonal variations are in agreement with the literature, comparisons between raw model outputs and observations, at the different measurement sites and for the specific observing periods, are contrasted. As the simulated meteorology at the scale of 10 km nicely captures the observed situations, the default set of surface characteristics (averaged at the resolution of a grid cell) appears to be one of the main reasons for the discrepancies found with observations. For each case, sensitivity studies have been performed in order to see the impact of adjusting the surface characteristics to the observed ones, when available. Generally, a correct agreement with the observations of deposition velocities is obtained. This advocates for a sub-grid scale representation of surface characteristics for the simulation of dry deposition velocities over such a complex area. Two other aspects appear in the discussion. Firstly, the strong influence of the soil water content to the plant

Dust cloud evolution in sub-stellar atmospheres via plasma deposition and plasma sputtering

Science.gov (United States)

Stark, C. R.; Diver, D. A.

2018-04-01

Context. In contemporary sub-stellar model atmospheres, dust growth occurs through neutral gas-phase surface chemistry. Recently, there has been a growing body of theoretical and observational evidence suggesting that ionisation processes can also occur. As a result, atmospheres are populated by regions composed of plasma, gas and dust, and the consequent influence of plasma processes on dust evolution is enhanced. Aim. This paper aims to introduce a new model of dust growth and destruction in sub-stellar atmospheres via plasma deposition and plasma sputtering. Methods: Using example sub-stellar atmospheres from DRIFT-PHOENIX, we have compared plasma deposition and sputtering timescales to those from neutral gas-phase surface chemistry to ascertain their regimes of influence. We calculated the plasma sputtering yield and discuss the circumstances where plasma sputtering dominates over deposition. Results: Within the highest dust density cloud regions, plasma deposition and sputtering dominates over neutral gas-phase surface chemistry if the degree of ionisation is ≳10-4. Loosely bound grains with surface binding energies of the order of 0.1-1 eV are susceptible to destruction through plasma sputtering for feasible degrees of ionisation and electron temperatures; whereas, strong crystalline grains with binding energies of the order 10 eV are resistant to sputtering. Conclusions: The mathematical framework outlined sets the foundation for the inclusion of plasma deposition and plasma sputtering in global dust cloud formation models of sub-stellar atmospheres.

Acid atmospheric deposition in a forested mountain catchment

Czech Academy of Sciences Publication Activity Database

Křeček, J.; Palán, L.; Stuchlík, Evžen

2017-01-01

Roč. 10, č. 4 (2017), s. 680-686 ISSN 1971-7458 Institutional support: RVO:60077344 Keywords : mountain water shed * spruce forests * acid atmospheric deposition * water resources recharge Subject RIV: DA - Hydrology ; Limnology OBOR OECD: Marine biology, freshwater biology, limnology Impact factor: 1.623, year: 2016

The Measurement of Dry Deposition and Surface Runoff to Quantify Urban Road Pollution in Taipei, Taiwan

Science.gov (United States)

Wang, Yunn-Jinn; Chen, Chi-Feng; Lin, Jen-Yang

2013-01-01

Pollutants deposited on road surfaces and distributed in the environment are a source of nonpoint pollution. Field data are traditionally hard to collect from roads because of constant traffic. In this study, in cooperation with the traffic administration, the dry deposition on and road runoff from urban roads was measured in Taipei City and New Taipei City, Taiwan. The results showed that the dry deposition is 2.01–5.14 g/m2·day and 78–87% of these solids are in the 75–300 µm size range. The heavy metals in the dry deposited particles are mainly Fe, Zn, and Na, with average concentrations of 34,978, 1,519 and 1,502 ppm, respectively. Elevated express roads show the highest heavy metal concentrations. Not only the number of vehicles, but also the speed of the traffic should be considered as factors that influence road pollution, as high speeds may accelerate vehicle wear and deposit more heavy metals on road surfaces. In addition to dry deposition, the runoff and water quality was analyzed every five minutes during the first two hours of storm events to capture the properties of the first flush road runoff. The sample mean concentration (SMC) from three roads demonstrated that the first flush runoff had a high pollution content, notably for suspended solid (SS), chemical oxygen demand (COD), oil and grease, Pb, and Zn. Regular sweeping and onsite water treatment facilities are suggested to minimize the pollution from urban roads. PMID:24135820

Seasonal and spatial variations of atmospheric trace elemental deposition in the Aliaga industrial region, Turkey

Science.gov (United States)

Kara, Melik; Dumanoglu, Yetkin; Altiok, Hasan; Elbir, Tolga; Odabasi, Mustafa; Bayram, Abdurrahman

2014-11-01

Atmospheric bulk deposition (wet + dry deposition) samples (n = 40) were collected concurrently at ten sites in four seasons between June 2009 and April 2010 in the Aliaga heavily industrialized region, Turkey, containing a number of significant air pollutant sources. Analyses of trace elements were carried out using inductively coupled plasma-mass spectrometry (ICP-MS). While there were significant differences in the particulate matter (PM) deposition fluxes among the sampling sites, seasonal variations were not statistically significant (Kruskal-Wallis test, p < 0.05). Both PM deposition and elemental fluxes were increased at the sampling sites in the vicinity of industrial activities. The crustal elements (i.e., Ca, Mg) and some anthropogenic elements (such as Fe, Zn, Mn, Pb, Cu, and Cr) were high, and the highest fluxes were mostly measured in summer and winter seasons. The enrichment factor (EF) and principal component analysis (PCA) was applied to the data to determine the possible sources in the study area. High EF values were obtained for the anthropogenic elements such as Ag, Cd, Zn, Pb, Cu and Sb. The possible sources were identified as anthropogenic sources (i.e., iron-steel production) (45.4%), crustal and re-suspended dust (27.1%), marine aerosol (7.9%), and coal and wood combustion (8.2%). Thus, the iron-steel production and its related activities were found to be the main pollutant sources for this region.

Estimating chemical composition of atmospheric deposition fluxes from mineral insoluble particles deposition collected in the western Mediterranean region

Directory of Open Access Journals (Sweden)

Y. Fu

2017-11-01

Full Text Available In order to measure the mass flux of atmospheric insoluble deposition and to constrain regional models of dust simulation, a network of automatic deposition collectors (CARAGA has been installed throughout the western Mediterranean Basin. Weekly samples of the insoluble fraction of total atmospheric deposition were collected concurrently on filters at five sites including four on western Mediterranean islands (Frioul and Corsica, France; Mallorca, Spain; and Lampedusa, Italy and one in the southern French Alps (Le Casset, and a weighing and ignition protocol was applied in order to quantify their mineral fraction. Atmospheric deposition is both a strong source of nutrients and metals for marine ecosystems in this area. However, there are few data on trace-metal deposition in the literature, since their deposition measurement is difficult to perform. In order to obtain more information from CARAGA atmospheric deposition samples, this study aimed to test their relevance in estimating elemental fluxes in addition to total mass fluxes. The elemental chemical analysis of ashed CARAGA filter samples was based on an acid digestion and an elemental analysis by inductively coupled plasma atomic emission spectroscopy (ICP-AES and mass spectrometry (MS in a clean room. The sampling and analytical protocols were tested to determine the elemental composition for mineral dust tracers (Al, Ca, K, Mg and Ti, nutrients (P and Fe and trace metals (Cd, Co, Cr, Cu, Mn, Ni, V and Zn from simulated wet deposition of dust analogues and traffic soot. The relative mass loss by dissolution in wet deposition was lower than 1 % for Al and Fe, and reached 13 % for P due to its larger solubility in water. For trace metals, this loss represented less than 3 % of the total mass concentration, except for Zn, Cu and Mn for which it could reach 10 %, especially in traffic soot. The chemical contamination during analysis was negligible for all the elements except for Cd

Continuous wet-only and dry-only deposition measurements of 137Cs and 7Be: an indicator of their origin

International Nuclear Information System (INIS)

Rosner, G.; Hoetzl, H.; Winkler, R.

1996-01-01

Series of monthly values of 137 Cs and 7 Be wet and dry deposition were measured with a wet-only and a dry-only collector each having an area of 2.25 m 2 . The results are presented for the period from November 1991 to May 1995. The behaviour of resuspended, Chernobyl-derived radiocesium is shown to be significantly different from that of cosmogenic 7 Be and from that of global fallout 137 Cs from nuclear weapons testing. The dry-to-total ratio of 0.65, the dry deposition velocity of 1.5 cm s -1 , the close correlation to the total amount of solids collected and the absence of a correlation between activity deposition and amount of rainfall point to a strong similarity in the deposition behaviour of present radiocesium and that of stable elements of terrestrial origin. (author)

Measurements of dry deposition rates of 212Pb from aerosols on various natural and artificial surfaces

International Nuclear Information System (INIS)

Osaki, S.; Sugihara, S.; Maeda, Y.; Osaki, T.

2007-01-01

The dry deposition rates on various grass fields and two forests have been measured by the use of 212 Pb (T 1/2 = 10.6 hours). The deposition rate on grass fields (average: 7 mm x s -1 ) roughly depends on the logarithms of the heights or densities of the grasses. The dry deposition rates on a broadleaved forest (Lithocarpus edulis) and a coniferous forest (Cryptomeria Japonica) were also measured. The highest (ave. 26 mm x s -1 ) was on the forest of C. Japonica because of the dense and adhesive surfaces of the leaves. (author)

Modeling of ammonia dry deposition downwind of a large poultry facility

Science.gov (United States)

This report describes a study investigating dry deposition of ammonia downwind of a poultry facility located on the southern perimeter of the Pocosin Lakes National Wildlife Refuge. This work is a component of a larger project conducted by the U.S. Fish and Wildlife Service: "Imp...

Compilation of information on uncertainties involved in deposition modeling

International Nuclear Information System (INIS)

Lewellen, W.S.; Varma, A.K.; Sheng, Y.P.

1985-04-01

The current generation of dispersion models contains very simple parameterizations of deposition processes. The analysis here looks at the physical mechanisms governing these processes in an attempt to see if more valid parameterizations are available and what level of uncertainty is involved in either these simple parameterizations or any more advanced parameterization. The report is composed of three parts. The first, on dry deposition model sensitivity, provides an estimate of the uncertainty existing in current estimates of the deposition velocity due to uncertainties in independent variables such as meteorological stability, particle size, surface chemical reactivity and canopy structure. The range of uncertainty estimated for an appropriate dry deposition velocity for a plume generated by a nuclear power plant accident is three orders of magnitude. The second part discusses the uncertainties involved in precipitation scavenging rates for effluents resulting from a nuclear reactor accident. The conclusion is that major uncertainties are involved both as a result of the natural variability of the atmospheric precipitation process and due to our incomplete understanding of the underlying process. The third part involves a review of the important problems associated with modeling the interaction between the atmosphere and a forest. It gives an indication of the magnitude of the problem involved in modeling dry deposition in such environments. Separate analytics have been done for each section and are contained in the EDB

Permissible annual depositions and radionuclide concentrations in air

International Nuclear Information System (INIS)

Belyaev, V.A.; Golovko, M.Yu.

1993-01-01

It is established that it necessary to take into account the other ways of radionuclide intake apart from the inhalation one when determining the standards for radionuclide contamination of the atmospheric air. Whereby it is proposed to standardize annual depositions rather than permissible concentration in the atmospheric air for the ways related to radionuclide releases on the ground surface, which is explained by ambiguity of their dry deposition rate from the air. Formulae and results of calculation of standard characteristics are presented. The permissible radionuclide depositions, related to the intake through food chains are calculated with account for diet diversity, agroclimatic and phenological parameters in different regions of the country

Atmospheric deposition and environmental quality in Italy

International Nuclear Information System (INIS)

Mosello, R.

1993-01-01

For Italy's Po River hydrological basin, artificial reservoirs have a great importance; water reserve is about 1600 million cubic meters for the hydroelectric reservoirs and about 76 million cubic meters for irrigation. Relevant to studies on water quality and acidification in the Po River Basin, this paper reviews some aspects of research on atmospheric deposition, i.e., geographical variability, long term trends, and effects on surface waters

The deposition of radioiodine onto rice plant from atmosphere

International Nuclear Information System (INIS)

Uchida, Shigeo; Muramatsu, Yasuyuki; Yoshida, Satoshi; Sumiya, Misako; Ohmomo, Yoichiro.

1994-01-01

Radiation dose estimations are usually made with the aid of assessment models in which model parameters such as the transfer factors of radionuclides from one environmental compartment to another are involved. In simple models the parameters are often described as the concentration ratio of a radionuclide between two compartments, when the system is under equilibrium condition. In this paper, the authors introduce the values of the parameters of radioiodine obtained by tracer experiments. Laboratory experiments on the transfer parameters of radionuclides from the atmosphere to rice plant were carried out in the atmosphere-to-crops system (deposition pathway). It is known that the typical chemical species of gaseous iodine in the atmosphere are elemental iodine (I 2 ) and methyliodide (CH 3 I). The deposition characteristics of both chemical species of gaseous iodine to rice grains were obtained. Mass normalized deposition velocity (V D ) and grain number normalized deposition velocity (V S ) of gaseous elemental iodine (I 2 ) and also methyliodide (CH 3 I) on unhulled rice were measured. Both V D and V S of methyliodide were about one percent of those of elemental iodine. Distribution pattern of methyliodide between unhulled rice and brown rice was significantly lower than that of elemental one. For wet deposition, we investigated the retention of radioiodines (iodide [I - ] and iodate [IO 3 - ] on rice grains and their translocation from the surface of the grains to brown rice. Though the ears were dipped into the solution containing 125 I - or 125 IO 3 - more than 15 min., both iodine species in the solutions were hardly taken up to the rice grains. The transfer rates of iodide and iodate, which are defined as 'the amount of the iodine in brown rice' divided by 'the amount of iodide in unhulled rice' were about 0.015 and 0.04, respectively. The rates were not changed with time after the radioiodine application. (author)

Potential geographic distribution of atmospheric nitrogen deposition from intensive livestock production in North Carolina, USA

International Nuclear Information System (INIS)

Costanza, Jennifer K.; Marcinko, Sarah E.; Goewert, Ann E.; Mitchell, Charles E.

2008-01-01

To examine the consequences of increased spatial aggregation of livestock production facilities, we estimated the annual production of nitrogen in livestock waste in North Carolina, USA, and analyzed the potential distribution of atmospheric nitrogen deposition from confined animal feeding operations ('CAFO') lagoons. North Carolina is a national center for industrial livestock production. Livestock is increasingly being raised in CAFOs, where waste is frequently held, essentially untreated, in open-air lagoons. Reduced nitrogen in lagoons is volatilized as ammonia (NH 3 ), transported atmospherically, and deposited to other ecosystems. The Albemarle-Pamlico Sound, NC, is representative of nitrogen-sensitive coastal waters, and is a major component of the second largest estuarine complex in the U.S. We used GIS to model the area of water in the Sound within deposition range of CAFOs. We also evaluated the number of lagoons within deposition range of each 1 km 2 grid cell of the state. We considered multiple scenarios of atmospheric transport by varying distance and directionality. Modeled nitrogen deposition rates were particularly elevated for the Coastal Plain. This pattern matches empirical data, suggesting that observed regional patterns of reduced nitrogen deposition can be largely explained by two factors: limited atmospheric transport distance, and spatial aggregation of CAFOs. Under our medium-distance scenario, a small portion (roughly 22%) of livestock production facilities contributes disproportionately to atmospheric deposition of nitrogen to the Albemarle-Pamlico Sound. Furthermore, we estimated that between 14-37% of the state receives 50% of the state's atmospheric nitrogen deposition from CAFO lagoons. The estimated total emission from livestock is 134,000 t NH 3 yr -1 , 73% of which originates from the Coastal Plain. Stronger waste management and emission standards for CAFOs, particularly those on the Coastal Plain nearest to sensitive water bodies

Wet and dry deposition and resuspension of AFCT/TFCT fuel processing radionuclides. Final report

International Nuclear Information System (INIS)

Slinn, W.G.N.; Katen, P.C.; Wolf, M.A.; Loveland, W.D.; Radke, L.F.; Miller, E.L.; Ghannam, L.J.; Reynolds, B.W.; Vickers, D.

1979-09-01

After short summary and introductory chapters, Chapter IV contains a critical analysis of available parameterizations for resuspension and for wet and dry removal processes and recommends interim parameterizations for use in radiation dose calculations. Chapter V describes methods and experimental results from field studies of in-cloud vs below-cloud scavenging, precipitation efficiency, and modifications of aerosols by clouds. In Chapter VI are contained descriptions of methods and results from four different approaches to the problem of measuring the dry deposition velocities of submicron aerosol particles depositing on vegetation. Chapter VII describes experimental results from a study of resuspension and weathering of tracer aerosol particles deposited on soil, grass and gravel; typical resuspension rates were found to be of the order of 10 -8 s -1 and it is recommended that the concept of weathering be reassessed. In Chapter VIII, National Weather Service data are used to obtain Lagrangian statistics for use in a regional-scale study of wet and dry removal. Chapter IX develops new concepts in reservoir models for application at regional to global scales. In the final chapter are some comments about the results found in this study and recommendations for future research

Effect of argon addition into oxygen atmosphere on YBCO thin films deposition

International Nuclear Information System (INIS)

Mozhaev, P. B.; Borisenko, I. V.; Ovsyannikov, G. A.; Kuehle, A.; Bindslev-Hansen, J.; Johannes, L.; Skov, J. L.

2002-01-01

Multicomponent nature of the YBa 2 Cu 3 O x (YBCO) high-temperature superconductor makes difficult fabrication of smooth thin films: every local deviation from stoichiometry can result in seeding of a non-superconducting oxide particle. High density of such particles on typical YBCO thin film surface, however, presumes overall non-stoichiometry of the film. Such an effect can result from (i) non-uniform material transport from target to substrate, and (ii) re-evaporation or re-sputtering from the growing film surface. The first reason is more usual for laser ablation deposition technique, the second is typical for long sputtering deposition processes. Substitution of oxygen with argon in the deposition atmosphere improves surface quality of YBCO thin films deposited both by laser ablation and DC-sputtering at high pressure techniques. In the first case, the ablated species are scattered different ways in the oxygen atmosphere. Addition of argon decreases the inelastic scattering of barium; the proper part of Ar in the deposition atmosphere makes scattering and, hence, transport of all atoms uniform. The YBCO films deposited by DC-sputtering at high pressure technique are Ba-deficient also, but the reason is re-sputtering of Ba from the growing film as a result of negative oxygen ions bombardment. Such bombardment can lead also to chemical interaction of the deposited material with the substrate, as in the case of deposition of YBCO thin film on the CeO 2 buffer layer on sapphire. Substitution of oxygen with argon not only suppresses ion bombardment of the film, but also increases discharge stability due to presence of positive Ar + ions. The limiting factor of argon substitution is sufficient oxygenation of the growing oxide film. When oxygen partial pressure is too small, the superconducting quality of the YBCO thin film decreases and such a decrease cannot be overcome by prolonged oxygenation after deposition. (Authors)

Dry deposition of O_3 and SO_2 estimated from gradient measurements above a temperate mixed forest

International Nuclear Information System (INIS)

Wu, Zhiyong; Staebler, Ralf; Vet, Robert; Zhang, Leiming

2016-01-01

Vertical profiles of O_3 and SO_2 concentrations were monitored at the Borden Forest site in southern Ontario, Canada from May 2008 to April 2013. A modified gradient method (MGM) was applied to estimate O_3 and SO_2 dry deposition fluxes using concentration gradients between a level above and a level below the canopy top. The calculated five-year mean (median) dry deposition velocity (V_d) were 0.35 (0.27) and 0.59 (0.54) cm s"−"1, respectively, for O_3 and SO_2. V_d(O_3) exhibited large seasonal variations with the highest monthly mean of 0.68 cm s"−"1 in August and the lowest of 0.09 cm s"−"1 in February. In contrast, seasonal variations of V_d(SO_2) were smaller with monthly means ranging from 0.48 (May) to 0.81 cm s"−"1 (December). The different seasonal variations between O_3 and SO_2 were caused by the enhanced SO_2 uptake by snow surfaces in winter. Diurnal variations showed a peak value of V_d in early morning in summer months for both O_3 and SO_2. Canopy wetness increased the non-stomatal uptake of O_3 while decreasing the stomatal uptake. This also applied to SO_2, but additional factors such as surface acidity also played an important role on the overall uptake. - Highlights: • Application of a modified gradient-method for quantifying dry deposition is demonstrated. • A five-year dry deposition database is developed for O_3 and SO_2 over a mixed forest. • Canopy wetness enhances non-stomatal O_3 uptake while inhibits stomatal uptake. • High surface acidity reduces SO_2 dry deposition. - Capsule: A five-year dataset of O_3 and SO_2 dry deposition velocities was generated from concentration gradient measurement data using a modified gradient method.

Estimation of nitrogen balance between the atmosphere and Lake Balaton and a semi natural grassland in Hungary

International Nuclear Information System (INIS)

Kugler, Sz.; Horvath, L.; Machon, A.

2008-01-01

The paper summarises the results to determine the fluxes of different N-compounds within the atmosphere and an aquatic and a terrestrial ecosystems, in Hungary. In the exchange processes of N-compounds between atmosphere and various ecosystems the deposition dominates. The net deposition fluxes are -730, -1 270 and -1530 mg N m -2 yr -1 for water, grassland, and forest ecosystems, respectively. For water, the main source of nitrogen compounds is the wet deposition. Ammonia gas is close to the equilibrium between the water and the air. For grassland the dry flux of nitric acid and ammonia is also an important term beside the wet deposition. Dry deposition to terrestrial ecosystems is roughly two times higher than wet deposition. A total of 8-10% of the nitrates and NH x deposited to terrestrial ecosystems are re-emitted into the air in the form of nitrous oxide (N 2 O) greenhouse gas. - The paper summarises the results of works to determine the N-flux between atmosphere and terrestrial/aquatic ecosystems in Hungary

Two dimensional radial gas flows in atmospheric pressure plasma-enhanced chemical vapor deposition

Science.gov (United States)

Kim, Gwihyun; Park, Seran; Shin, Hyunsu; Song, Seungho; Oh, Hoon-Jung; Ko, Dae Hong; Choi, Jung-Il; Baik, Seung Jae

2017-12-01

Atmospheric pressure (AP) operation of plasma-enhanced chemical vapor deposition (PECVD) is one of promising concepts for high quality and low cost processing. Atmospheric plasma discharge requires narrow gap configuration, which causes an inherent feature of AP PECVD. Two dimensional radial gas flows in AP PECVD induces radial variation of mass-transport and that of substrate temperature. The opposite trend of these variations would be the key consideration in the development of uniform deposition process. Another inherent feature of AP PECVD is confined plasma discharge, from which volume power density concept is derived as a key parameter for the control of deposition rate. We investigated deposition rate as a function of volume power density, gas flux, source gas partial pressure, hydrogen partial pressure, plasma source frequency, and substrate temperature; and derived a design guideline of deposition tool and process development in terms of deposition rate and uniformity.

Atmospheric pulsed laser deposition of plasmonic nanoparticle films of silver with flowing gas and flowing atmospheric plasma

Science.gov (United States)

Khan, T. M.; Pokle, A.; Lunney, J. G.

2018-04-01

Two methods of atmospheric pulsed laser deposition of plasmonic nanoparticle films of silver are described. In both methods the ablation plume, produced by a 248 nm, 20 ns excimer laser in gas, is strongly confined near the target and forms a nanoparticle aerosol. For both the flowing gas, and the atmospheric plasma from a dielectric barrier discharge plasma source, the aerosol is entrained in the flow and carried to a substrate for deposition. The nanoparticle films produced by both methods were examined by electron microscopy and optical absorption spectroscopy. With plasma assistance, the deposition rate was significantly enhanced and the film morphology altered. With argon gas, isolated nanoparticles of 20 nm size were obtained, whereas in argon plasma, the nanoparticles are aggregated in clusters of 90 nm size. Helium gas also leads to the deposition of isolated nanoparticles, but with helium plasma, two populations of nanoparticles are observed: one of rounded particles with a mean size of 26 nm and the other of faceted particles with a mean size 165 nm.

Atmospheric deposition of radioactive cesium (137Cs) associated with dust events in East Asia

International Nuclear Information System (INIS)

Fujiwara, H.

2010-01-01

Since the cessation of atmospheric nuclear testing in 1980, there has been no known serious atmospheric contamination by radioactive cesium (sup(137)Cs) apart from the Chernobyl nuclear reactor accident in 1986. There now remain only small amounts of anthropogenic radionuclides in the atmosphere that can be directly related to past testing. However, sup(137)Cs is still regularly found in atmospheric deposition samples in Japan. In this study, we analyzed sup(137)Cs monitoring data, meteorological data, and field survey results to investigate the recent transport and deposition of sup(137)Cs associated with dust phenomena. Monthly records of nationwide sup(137)Cs deposition in Japan during the 1990s show a consistent seasonal variation, with higher levels of deposition occurring in spring. In March 2002, an unexpectedly high amount of sup(137)Cs was deposited in the northwestern coastal area of Japan at the same time as an Asian dust event was observed. Analysis of land-based weather data showed that sandstorms and other dust-raising phenomena also occurred in March 2002 over areas of Mongolia and northeastern China where grassland and shrubs predominated. Furthermore, radioactivity measurements showed sup(137)Cs enrichment in the surface layer of grassland soils in the areas affected by these sandstorms. These results suggest that grasslands are potential sources of sup(137)Cs-bearing dust. Continued desertification of the East Asian continent in response to recent climate change can be expected to result in an increase in sup(137)Cs-bearing soil particles in the atmosphere, and their subsequent re-deposition in Japan. However, soil dust is also raised around Japanese monitoring sites by the strong winds that are common in Japan in spring, and this local dust might also contribute to sup(137)Cs deposition in Japan. To estimate the relative contributions of local and distant dust events to the total sup(137)Cs deposition, we monitored deposition of mineral particles

Characterization of soil fauna under the influence of mercury atmospheric deposition in Atlantic Forest, Rio de Janeiro, Brazil.

Science.gov (United States)

Buch, Andressa Cristhy; Correia, Maria Elizabeth Fernandes; Teixeira, Daniel Cabral; Silva-Filho, Emmanoel Vieira

2015-06-01

The increasing levels of mercury (Hg) found in the atmosphere arising from anthropogenic sources, have been the object of great concern in the past two decades in industrialized countries. Brazil is the seventh country with the highest rate of mercury in the atmosphere. The major input of Hg to ecosystems is through atmospheric deposition (wet and dry), being transported in the atmosphere over large distances. The forest biomes are of strong importance in the atmosphere/soil cycling of elemental Hg through foliar uptake and subsequent transference to the soil through litter, playing an important role as sink of this element. Soil microarthropods are keys to understanding the soil ecosystem, and for such purpose were characterized by the soil fauna of two Units of Forest Conservation of the state of the Rio de Janeiro, inwhich one of the areas suffer quite interference from petrochemicals and industrial anthropogenic activities and other area almost exempts of these perturbations. The results showed that soil and litter of the Atlantic Forest in Brazil tend to stock high mercury concentrations, which could affect the abundance and richness of soil fauna, endangering its biodiversity and thereby the functioning of ecosystems. Copyright © 2015. Published by Elsevier B.V.

Contribution of foliar leaching and dry deposition to sulfate in net throughfall below deciduous trees

International Nuclear Information System (INIS)

Garten, C.T. Jr.; Bondietti, E.A.; Lomax, R.D.

1988-01-01

Experiments were conducted at Walker Branch Watershed, Tennessee in 1986 with radioactive 35 S to quantify the contribution of foliar leaching and dry deposition to sulfate (SO 4 2- ) in net throughfall (NTF). Two red maple (Acer rubrum) and two yellow poplar (Liriodendron tulipifera) trees (12-15 m tall) were radiolabeled by stem well injection. Total S and 35 S were measured in leaves; 35 S and SO 4 2- were measured in throughfall (THF). The contribution of foliar leaching to SO 4 2- in NTF, THF minus incident precipitation, was estimated by isotope dilution of 35 S in NTF arising from nonradioactive S in dry deposition. The per cent contribution of foliar leaching to SO 4 2- in NTF was greatest during the week following isotope labeling and during the period of autumn leaf fall. During the growing season, foliar leaching accounted for 80% of the SO 4 2- in NTF beneath the study trees. Dry deposition of S to these tree species can be reasonably approximated during summer from the measurement of SO 4 2- flux in NTF. (author)

Foliar loading and metabolic assimilation of dry deposited nitric acid air pollutants by trees

Science.gov (United States)

Pamela E. Padgett; Hillary Cook; Andrzej Bytnerowicz; Robert L. Heath

2009-01-01

Dry deposition of nitric acid vapor (HNO(3)) is a major contributor to eutrophication of natural ecosystems. Although soil fertilization by nitrogen deposition is considered to be the primary pathway for changes in plant nutrient status and shifts in ecological structure, the aerial portion of plants offer many times the surface area in which to...

Letter to the editor: Critical assessments of the current state of scientific knowledge, terminology, and research needs concerning the ecological effects of elevated atmospheric nitrogen deposition in China

Science.gov (United States)

Pan, Yuepeng; Liu, Yongwen; Wentworth, Gregory R.; Zhang, Lin; Zhao, Yuanhong; Li, Yi; Liu, Xuejun; Du, Enzai; Fang, Yunting; Xiao, Hongwei; Ma, Hongyuan; Wang, Yuesi

2017-03-01

In a publication in Atmospheric Environment (http://dx.doi.org/10.1016/j.atmosenv.2015.10.081), Gu et al. (2015) estimated that "the total nitrogen (N) deposition in 2010 was 2.32 g N m-2 yr-1" in China. This value is comparable with previous estimations based on a synthesized dataset of wet/bulk inorganic N deposition observations, which underestimates the total N deposition since their algorithm (equations (2) and (3) in their paper) does not account for dry deposition of NH3, HNO3, NOx and wet/dry deposition of HONO and organic nitrogen (e.g. amines, amides, PAN). Indeed, Gu et al. (2015) mixed the terminology of wet/bulk deposition and total deposition. Another flawed assumption by Gu et al. (2015) is that all inorganic N in precipitation estimated by their algorithm originates from fertilizer and coal combustion. This is incorrect and almost certainly causes biases in the spatial and temporal distribution of estimated wet/bulk inorganic N deposition (Fig. 5 in their paper), further considering the fact that they neglected important N sources like livestock and they did not consider the nonlinearity between various sources and deposition. Besides the input data on N deposition, the model validation (Sect. 2.3.2) described in their paper also requires clarification because the detailed validation information about the time series of observational dataset versus modeling results was not given. As a result of these combined uncertainties in their estimation of N deposition and the lack of detail for model-measurement comparison, their estimates of the impacts of N deposition on carbon storage in Chinese forests may need further improvement. We suggest the clarification of the terminology regarding N deposition, especially for wet deposition, bulk deposition, gaseous and particulate dry deposition or total deposition since the accurate distinction between these terms is crucial to investigating and estimating the effects of N deposition on ecosystems.

Seasonal atmospheric deposition and air-sea gas exchange of polycyclic aromatic hydrocarbons over the Yangtze River Estuary, East China Sea: Implications for source-sink processes

Science.gov (United States)

Jiang, Yuqing; Lin, Tian; Wu, Zilan; Li, Yuanyuan; Li, Zhongxia; Guo, Zhigang; Yao, Xiaohong

2018-04-01

In this work, air samples and surface seawater samples covering four seasons from March 2014 to January 2015 were collected from a background receptor site in the YRE to explore the seasonal fluxes of air-sea gas exchange and dry and wet deposition of 15 polycyclic aromatic hydrocarbons (PAHs) and their source-sink processes at the air-sea interface. The average dry and wet deposition fluxes of 15 PAHs were estimated as 879 ± 1393 ng m-2 d-1 and 755 ± 545 ng m-2 d-1, respectively. Gaseous PAH release from seawater to the atmosphere averaged 3114 ± 1999 ng m-2 d-1 in a year round. The air-sea gas exchange of PAHs was the dominant process at the air-sea interface in the YRE as the magnitude of volatilization flux of PAHs exceeded that of total dry and wet deposition. The gas PAH exchange flux was dominated by three-ring PAHs, with the highest value in summer and lowest in winter, indicating a marked seasonal variation owing to differences in Henry's law constants associated with temperature, as well as wind speed and gaseous-dissolved gradient among seasons. Based on the simplified mass balance estimation, a net 11 tons y-1 of PAHs (mainly three-ring PAHs) were volatilized from seawater to the atmosphere in a ∼20,000 km2 area in the YRE. Other than the year-round Yangtze River input and ocean ship emissions, the selective release of low-molecular-weight PAHs from bottom sediments in winter due to resuspension triggered by the East Asian winter monsoon is another potential source of PAHs. This work suggests that the source-sink processes of PAHs at the air-sea interface in the YRE play a crucial role in regional cycling of PAHs.

Mosses as an integrating tool for monitoring PAH atmospheric deposition: comparison with total deposition and evaluation of bioconcentration factors. A year-long case-study.

Science.gov (United States)

Foan, Louise; Domercq, Maria; Bermejo, Raúl; Santamaría, Jesús Miguel; Simon, Valérie

2015-01-01

Polycyclic aromatic hydrocarbon (PAH) atmospheric deposition was evaluated at a remote site in Northern Spain using moss biomonitoring with Hylocomium splendens (Hedw.) Schimp., and by measuring the total deposition fluxes of PAHs. The year-long study allowed seasonal variations of PAH content in mosses to be observed, and these followed a similar trend to those of PAH fluxes in total deposition. Generally, atmospheric deposition of PAHs is greater in winter than in summer, due to more PAH emissions from domestic heating, less photoreactivity of the compounds, and intense leaching of the atmosphere by wet deposition. However, fractionation of these molecules between the environmental compartments occurs: PAH fluxes in total deposition and PAH concentrations in mosses are correlated with their solubility (r=0.852, pPAH fluxes can be estimated with moss biomonitoring data if the bioconcentration or 'enriching' factors are known. Copyright © 2014 Elsevier Ltd. All rights reserved.

Comparison between dry deposition fluxes measured with water and solid surfaces, and estimated by an inferential model

Energy Technology Data Exchange (ETDEWEB)

Balestrini, R.; Consuma, A.; Polesello, S.; Tartari, G. [Istituto di Ricerca sulle Acque, Brugherio, MI (Italy)

2000-08-01

The quantification of the dry atmospheric input to natural surfaces is currently a complete task. In this study a water surface sampler (Das) was used contemporary to conventional solid surface samplers (wet and dry and bulk) to monitor the dry deposition in a densely inhabited and industrialised area. The dry contribution to the total deposition was 33-56% for sulfate, 11-39% for ammonium and 18-28% for nitrate ion, depending on the measurement technique. Among the three samplers, the Das one was the most efficient to collect sulfate, ammonium and nitrate. The comparison of the seasonal trends showed that the dry collector using a polyethylene surface, collected mainly aerosol particles of ammonium sulfate, while the aqueous surface of Das sampler was able to sample also the gaseous form of the pollutants. Sulfate and nitrate flux values determined from direct measurements were also compared with those obtained by a resistance model. The sulphate measured values fitted quite well with those predicted from the model showing similar seasonal variations. The quantitative differences observed in winter could be due to an increase in the acidity of water, used as collecting medium, which lowered the solubility of gaseous sulphur dioxide. In order to investigate the effect of water acidity on the deposition on a water body, a series of experiments were carried out. [Italian] La quantificazione della deposizione secca costituisce, ancora oggi, un'operazione complessa. Tre tipi di campionatori, rispettivamente con una superficie acquosa (Das) e con superfici solide in polietilene (wet and dry e bulk) sono stati impiegati per misurare la deposizione secca in un'area densamente antropizzata. Il contributo della deposizione secca alla deposizione totale e' risultato compreso tra 33 e 56% per i solfati, tra 11 e 39% per l'ammonio e tra 18 e il 28% per i nitrati, secondo la tecnica di campionamento. Il campionatore Das si e' dimostrato il piu

Aerosol dynamics within and above forest in relation to turbulent transport and dry deposition

DEFF Research Database (Denmark)

Rannik, Üllar; Zhou, Luxi; Zhou, Putian

2016-01-01

of 10 days in May 2013 to a pine forest site in southern Finland. The period was characterized by frequent new particle formation events and simultaneous intensive aerosol transformation. The aim of the study was to analyze and quantify the role of aerosol and ABL dynamics in the vertical transport...... of aerosols. It was of particular interest to what extent the fluxes above the canopy deviate from the particle dry deposition on the canopy foliage due to the above-mentioned processes. The model simulations revealed that the particle concentration change due to aerosol dynamics frequently exceeded...... the effect of particle deposition by even an order of magnitude or more. The impact was, however, strongly dependent on particle size and time. In spite of the fact that the timescale of turbulent transfer inside the canopy is much smaller than the timescales of aerosol dynamics and dry deposition, leading...

Atmospheric deposition, CO2, and change in the land carbon sink

DEFF Research Database (Denmark)

Martinez-Fernandez, Cristina; Vicca, Sara; Janssens, Ivan A.

2017-01-01

Concentrations of atmospheric carbon dioxide (CO2) have continued to increase whereas atmospheric deposition of sulphur and nitrogen has declined in Europe and the USA during recent decades. Using time series of flux observations from 23 forests distributed throughout Europe and the USA, and gene...... show the need to include the effects of changing atmospheric composition, beyond CO2, to assess future dynamics of carbon-climate feedbacks not currently considered in earth system/climate modelling....

Worldwide dispersion and deposition of radionuclides produced in atmospheric tests.

Science.gov (United States)

Bennett, Burton G

2002-05-01

Radionuclides produced in atmospheric nuclear tests were widely dispersed in the global environment. From the many measurements of the concentrations in air and the deposition amounts, much was learned of atmospheric circulation and environmental processes. Based on these results and the reported fission and total yields of individual tests, it has been possible to devise an empirical model of the movement and residence times of particles in the various atmospheric regions. This model, applied to all atmospheric weapons tests, allows extensive calculations of air concentrations and deposition amounts for the entire range of radionuclides produced throughout the testing period. Especially for the shorter-lived fission radionuclides, for which measurement results at the time of the tests are less extensive, a more complete picture of levels and isotope ratios can be obtained, forming a basis for improved dose estimations. The contributions to worldwide fallout can be inferred from individual tests, from tests at specific sites, or by specific countries. Progress was also made in understanding the global hydrological and carbon cycles from the tritium and 14C measurements. A review of the global measurements and modeling results is presented in this paper. In the future, if injections of materials into the atmosphere occur, their anticipated motions and fates can be predicted from the knowledge gained from the fallout experience.

Characterisation of atmospheric deposited particles during a dust storm in urban areas of Eastern Australia

Energy Technology Data Exchange (ETDEWEB)

Gunawardena, Janaka, E-mail: j.gunawardena@qut.edu.au; Ziyath, Abdul M., E-mail: mohamed.ziyath@qut.edu.au; Bostrom, Thor E., E-mail: t.bostrom@qut.edu.au; Bekessy, Lambert K., E-mail: l.bekessy@qut.edu.au; Ayoko, Godwin A., E-mail: g.ayoko@qut.edu.au; Egodawatta, Prasanna, E-mail: p.egodawatta@qut.edu.au; Goonetilleke, Ashantha, E-mail: a.goonetilleke@qut.edu.au

2013-09-01

The characteristics of dust particles deposited during the 2009 dust storm in the Gold Coast and Brisbane regions of Australia are discussed in this paper. The study outcomes provide important knowledge in relation to the potential impacts of dust storm related pollution on ecosystem health in the context that the frequency of dust storms is predicted to increase due to anthropogenic desert surface modifications and climate change impacts. The investigated dust storm contributed a large fraction of fine particles to the environment with an increased amount of total suspended solids, compared to dry deposition under ambient conditions. Although the dust storm passed over forested areas, the organic carbon content in the dust was relatively low. The primary metals present in the dust storm deposition were aluminium, iron and manganese, which are common soil minerals in Australia. The dust storm deposition did not contain significant loads of nickel, cadmium, copper and lead, which are commonly present in the urban environment. Furthermore, the comparison between the ambient and dust storm chromium and zinc loads suggested that these metals were contributed to the dust storm by local anthropogenic sources. The potential ecosystem health impacts of the 2009 dust storm include, increased fine solids deposition on ground surfaces resulting in an enhanced capacity to adsorb toxic pollutants as well as increased aluminium, iron and manganese loads. In contrast, the ecosystem health impacts related to organic carbon and other metals from dust storm atmospheric deposition are not considered to be significant. - Highlights: • The dust storm contributed a large fraction of fine particles to pollutant build-up. • The dust storm increased TSS, Al, Fe and Mn loads in build-up on ground surfaces. • Dust storm did not significantly increase TOC, Ni, Cu, Pb and Cd loads in build-up. • Cr and Zn in dust storm deposition were contributed by local anthropogenic sources.

Characterisation of atmospheric deposited particles during a dust storm in urban areas of Eastern Australia

International Nuclear Information System (INIS)

Gunawardena, Janaka; Ziyath, Abdul M.; Bostrom, Thor E.; Bekessy, Lambert K.; Ayoko, Godwin A.; Egodawatta, Prasanna; Goonetilleke, Ashantha

2013-01-01

The characteristics of dust particles deposited during the 2009 dust storm in the Gold Coast and Brisbane regions of Australia are discussed in this paper. The study outcomes provide important knowledge in relation to the potential impacts of dust storm related pollution on ecosystem health in the context that the frequency of dust storms is predicted to increase due to anthropogenic desert surface modifications and climate change impacts. The investigated dust storm contributed a large fraction of fine particles to the environment with an increased amount of total suspended solids, compared to dry deposition under ambient conditions. Although the dust storm passed over forested areas, the organic carbon content in the dust was relatively low. The primary metals present in the dust storm deposition were aluminium, iron and manganese, which are common soil minerals in Australia. The dust storm deposition did not contain significant loads of nickel, cadmium, copper and lead, which are commonly present in the urban environment. Furthermore, the comparison between the ambient and dust storm chromium and zinc loads suggested that these metals were contributed to the dust storm by local anthropogenic sources. The potential ecosystem health impacts of the 2009 dust storm include, increased fine solids deposition on ground surfaces resulting in an enhanced capacity to adsorb toxic pollutants as well as increased aluminium, iron and manganese loads. In contrast, the ecosystem health impacts related to organic carbon and other metals from dust storm atmospheric deposition are not considered to be significant. - Highlights: • The dust storm contributed a large fraction of fine particles to pollutant build-up. • The dust storm increased TSS, Al, Fe and Mn loads in build-up on ground surfaces. • Dust storm did not significantly increase TOC, Ni, Cu, Pb and Cd loads in build-up. • Cr and Zn in dust storm deposition were contributed by local anthropogenic sources

Watershed-scale changes in terrestrial nitrogen cycling during a period of decreased atmospheric nitrate and sulfur deposition

Science.gov (United States)

Sabo, Robert D.; Scanga, Sara E.; Lawrence, Gregory B.; Nelson, David M.; Eshleman, Keith N.; Zabala, Gabriel A.; Alinea, Alexandria A.; Schirmer, Charles D.

2016-01-01

Recent reports suggest that decreases in atmospheric nitrogen (N) deposition throughout Europe and North America may have resulted in declining nitrate export in surface waters in recent decades, yet it is unknown if and how terrestrial N cycling was affected. During a period of decreased atmospheric N deposition, we assessed changes in forest N cycling by evaluating trends in tree-ring δ15N values (between 1980 and 2010; n = 20 trees per watershed), stream nitrate yields (between 2000 and 2011), and retention of atmospherically-deposited N (between 2000 and 2011) in the North and South Tributaries (North and South, respectively) of Buck Creek in the Adirondack Mountains, USA. We hypothesized that tree-ring δ15N values would decline following decreases in atmospheric N deposition (after approximately 1995), and that trends in stream nitrate export and retention of atmospherically deposited N would mirror changes in tree-ring δ15N values. Three of the six sampled tree species and the majority of individual trees showed declining linear trends in δ15N for the period 1980–2010; only two individual trees showed increasing trends in δ15N values. From 1980 to 2010, trees in the watersheds of both tributaries displayed long-term declines in tree-ring δ15N values at the watershed scale (R = −0.35 and p = 0.001 in the North and R = −0.37 and p <0.001 in the South). The decreasing δ15N trend in the North was associated with declining stream nitrate concentrations (−0.009 mg N L−1 yr−1, p = 0.02), but no change in the retention of atmospherically deposited N was observed. In contrast, nitrate yields in the South did not exhibit a trend, and the watershed became less retentive of atmospherically deposited N (−7.3% yr−1, p < 0.001). Our δ15N results indicate a change in terrestrial N availability in both watersheds prior to decreases in atmospheric N deposition, suggesting that decreased atmospheric N deposition was not the sole driver of

Tracing the Atmospheric Source of Desert Nitrates Using Δ 17O

Science.gov (United States)

Michalski, G. M.; Holve, M.; Feldmeier, J.; Bao, H.; Reheis, M.; Bockheim, J. G.; Thiemens, M. H.

2001-05-01

Mineral, caliche, and soil nitrates are found throughout the worlds deserts, including the cold dry Wright Valley of Antarctica, the Atacama desert in Chile and the Mojave desert in the southwest United States. Several authors have suggested biologic sources of these nitrates while others have postulated atmospheric deposition. A recent study utilizing 18O indicated that 30%, and perhaps 100%, of nitrates found in the Atacama and Mojave were of atmospheric origin [1]. A more quantitative assessment of the source strength of atmospheric nitrates was impossible because of the high variability of δ 18 18O of atmospheric nitrates and uncertainties in conditions of biologic production. Mass independently fractionated (MIF) processes are defined and quantified by the equation Δ 17O = δ 17O - .52x δ 18O. MIF processes are associated with the photochemistry of trace gases in the atmosphere and have been found in O3, N2O, CO, and sulfate aerosols . A large MIF (Δ 17O ~ 28 ‰ ) in nitrate aerosols collected in polluted regions was recently reported [2]. Here we extend measurements of MIF in nitrate to the dry deposition of nitrate in less polluted areas (Mojave desert). In addition we trace the MIF signal as it accumulates in the regolith as nitrate salts and minerals and is mixed with biologically produced nitrate (nitrification). Also examined were the isotopic composition of soil nitrates from Antarctic dry valleys. Dust samples were collected as part of the NADP program and soils were collected throughout the Mojave and Death Valley regions of California. Isotope analysis was done in addition to soluble ion content (Cl, NO3, SO4). Dust samples collected by dry deposition samplers showed a large MIF > 20‰ approaching values measured in urban nitrate aerosol. Soils collected throughout the region showed large variations in Δ 17O from ~ 0 to 18 ‰ . The low Δ 17O values are nitrates dominated by biologic nitrification and higher values are nitrates derived by

Responses of Surface Ozone Air Quality to Anthropogenic Nitrogen Deposition

Science.gov (United States)

Zhang, L.; Zhao, Y.; Tai, A. P. K.; Chen, Y.; Pan, Y.

2017-12-01

Human activities have substantially increased atmospheric deposition of reactive nitrogen to the Earth's surface, inducing unintentional effects on ecosystems with complex environmental and climate consequences. One consequence remaining unexplored is how surface air quality might respond to the enhanced nitrogen deposition through surface-atmosphere exchange. We combine a chemical transport model (GEOS-Chem) and a global land model (Community Land Model) to address this issue with a focus on ozone pollution in the Northern Hemisphere. We consider three processes that are important for surface ozone and can be perturbed by addition of atmospheric deposited nitrogen: emissions of biogenic volatile organic compounds (VOCs), ozone dry deposition, and soil nitrogen oxide (NOx) emissions. We find that present-day anthropogenic nitrogen deposition (65 Tg N a-1 to the land), through enhancing plant growth (represented as increases in vegetation leaf area index (LAI) in the model), could increase surface ozone from increased biogenic VOC emissions, but could also decrease ozone due to higher ozone dry deposition velocities. Meanwhile, deposited anthropogenic nitrogen to soil enhances soil NOx emissions. The overall effect on summer mean surface ozone concentrations show general increases over the globe (up to 1.5-2.3 ppbv over the western US and South Asia), except for some regions with high anthropogenic NOx emissions (0.5-1.0 ppbv decreases over the eastern US, Western Europe, and North China). We compare the surface ozone changes with those driven by the past 20-year climate and historical land use changes. We find that the impacts from anthropogenic nitrogen deposition can be comparable to the climate and land use driven surface ozone changes at regional scales, and partly offset the surface ozone reductions due to land use changes reported in previous studies. Our study emphasizes the complexity of biosphere-atmosphere interactions, which can have important

Measurements of ammonia concentrations, fluxes and dry deposition velocities to a spruce forest 1991-1995

DEFF Research Database (Denmark)

Andersen, H.V.; Hovmand, M.F.; Hummelshøj, P.

1999-01-01

The dry deposition velocities and fluxes of ammonia have been estimated from measurements of the vertical gradient of ammonia and micrometeorology above a spruce forest in western Jutland, Denmark. Measurements have been made in seven periods, each lasting about one week and covering all seasons...... measuring period characterized by easterly winds with dry conditions and high ammonia concentrations, and the emissions might relate to evaporation from ammonia saturated surfaces or emission from mineralization in the forest soil. In general, relatively high net deposition velocities were observed during...... at conditions with easterly winds, the air have passed central Jutland with large emission areas. Some of the relatively low deposition velocities or emissions were observed during conditions with low ammonia concentration and westerly winds. These observations might relate to a compensation point of the forest...

Atmospheric nitrogen deposition in world biodiversity hotspots: the need for a greater global perspective in assessing N deposition impacts

NARCIS (Netherlands)

Phoenix, G.K.; Hicks, W.K.; Cinderby, S.; Kuylenstierna, J.C.I.; Stock, W.D.; Dentener, F.J.; Giller, K.E.; Austin, A.T.; Lefroy, R.D.B.; Gimeno, B.S.; Ashmore, M.R.; Ineson, P.

2006-01-01

Increased atmospheric nitrogen (N) deposition is known to reduce plant diversity in natural and semi-natural ecosystems, yet our understanding of these impacts comes almost entirely from studies in northern Europe and North America. Currently, we lack an understanding of the threat of N deposition

Parallel measurements of organic and elemental carbon dry (PM1, PM2.5) and wet (rain, snow, mixed) deposition into the Baltic Sea.

Science.gov (United States)

Witkowska, Agnieszka; Lewandowska, Anita; Falkowska, Lucyna M

2016-03-15

Parallel studies on organic and elemental carbon in PM1 and PM2.5 aerosols and in wet deposition in various forms of its occurrence were conducted in the urbanised coastal zone of the Baltic Sea. The carbon load introduced into the sea water was mainly affected by the form of precipitation. Dry deposition load of carbon was on average a few orders of magnitude smaller than wet deposition. The suspended organic carbon was more effectively removed from the air with rain than snow, while an inverse relationship was found for elemental carbon. However the highest flux of water insoluble organic carbon was recorded in precipitation of a mixed nature. The atmospheric cleaning of highly dissolved organic carbon was observed to be the most effective on the first day of precipitation, while the hydrophobic elemental carbon was removed more efficiently when the precipitation lasted longer than a day. Copyright © 2016 Elsevier Ltd. All rights reserved.

The model of atmospheric diffusion and deposition adopted for the German reactor risk study (phase A)

International Nuclear Information System (INIS)

Huebschmann, W.G.; Vogt, S.

1980-01-01

The consequence model of the German reactor risk study comprises the release of radioactivity and thermal energy from the containment, the atmospheric diffusion, and the deposition of activity on the ground, the calculation of dose equivalents induced via the main exposure pathways, and the calculation of early and late health effects to the population, taking into account emergency actions for the protection of the public. The following exposure pathways are included in the model: external irradiation from the passing cloud and from the activity deposited on the ground, inhalation of the cloud activity and of resuspended material, and ingestion of contaminated food. Account is taken of the following effects: building wake, plume rise to thermal energy release, dynamic change of diffusion parameters, and plume depletion due to radioactive decay, dry and wet deposition. The calculations are performed for 115 weather sequences with starting times evenly distributed over one year. It is shown that such a choice of weather sequences reflects the total variety of meteorological situations, including precipitation, in a statistically adequate way. The area of the Federal Republic of Germany is divided into four meteorological site-regions, each with typical meteorological characteristics. Each power reactor site is assigned to one of the meteorological site-regions

Effects of atmospheric deposition of pesticides on terrestrial organisms in the Netherlands

NARCIS (Netherlands)

Jong FMW de; Luttik R; SEC

2004-01-01

At present there is much focus on the atmospheric dispersal of pesticides. However, there is very little known about the effects of atmospheric deposition, especially in terrestrial ecosystems. In the study described here, a start has been made to clarify the possible effects on terrestrial

Influence of radioactive contamination to agricultural products due to dry and wet deposition processes during a nuclear emergency

International Nuclear Information System (INIS)

Hwang, Won Tae; Kim, Eun Han; Suh, Kyung Suk; Han, Moon Hee; Choi, Yong Ho; Lee, Chang Woo

2002-01-01

Combined with deposition model onto the ground of radionuclides, the influence of radioactive contamination to agricultural products was analyzed due to wet deposition as well as dry deposition from radioactive air concentration during a nuclear emergency. The previous dynamic food chain model, in which initial input parameter is only radionuclide concentrations on the ground, was improved for the evaluating of radioactive contamination to agricultural products from either radionuclide concentrations in air or radionuclide concentrations on the ground. As the results, in case of deposition onto the ground, wet deposition was more dominant process than dry deposition. While the contamination levels of agricultural products were dependent on the a variety of factors such as radionuclides and rainfall rate. It means that the contamination levels of agricultural products are determined from which is more dominant process between deposition on the ground and interception onto agricultural plants

CO2 deficit in temperate forest soils receiving high atmospheric N-deposition.

Science.gov (United States)

Fleischer, Siegfried

2003-02-01

Evidence is provided for an internal CO2 sink in forest soils, that may have a potential impact on the global CO2-budget. Lowered CO2 fraction in the soil atmosphere, and thus lowered CO2 release to the aboveground atmosphere, is indicated in high N-deposition areas. Also at forest edges, especially of spruce forest, where additional N-deposition has occurred, the soil CO2 is lowered, and the gradient increases into the closed forest. Over the last three decades the capacity of the forest soil to maintain the internal sink process has been limited to a cumulative supply of approximately 1000 and 1500 kg N ha(-1). Beyond this limit the internal soil CO2 sink becomes an additional CO2 source, together with nitrogen leaching. This stage of "nitrogen saturation" is still uncommon in closed forests in southern Scandinavia, however, it occurs in exposed forest edges which receive high atmospheric N-deposition. The soil CO2 gradient, which originally increases from the edge towards the closed forest, becomes reversed.

Investigation of deposition characteristics and properties of high-rate deposited silicon nitride films prepared by atmospheric pressure plasma chemical vapor deposition

International Nuclear Information System (INIS)

Kakiuchi, H.; Nakahama, Y.; Ohmi, H.; Yasutake, K.; Yoshii, K.; Mori, Y.

2005-01-01

Silicon nitride (SiN x ) films have been prepared at extremely high deposition rates by the atmospheric pressure plasma chemical vapor deposition (AP-PCVD) technique on Si(001) wafers from gas mixtures containing He, H 2 , SiH 4 and N 2 or NH 3 . A 150 MHz very high frequency (VHF) power supply was used to generate high-density radicals in the atmospheric pressure plasma. Deposition rate, composition and morphology of the SiN x films prepared with various deposition parameters were studied by scanning electron microscopy and Auger electron spectroscopy. Fourier transformation infrared (FTIR) absorption spectroscopy was also used to characterize the structure and the chemical bonding configurations of the films. Furthermore, etching rate with buffered hydrofluoric acid (BHF) solution, refractive index and capacitance-voltage (C-V) characteristics were measured to evaluate the dielectric properties of the films. It was found that effective passivation of dangling bonds and elimination of excessive hydrogen atoms at the film-growing surface seemed to be the most important factor to form SiN x film with a dense Si-N network. The C-V curve of the optimized film showed good interface properties, although further improvement was necessary for use in the industrial metal-insulator-semiconductor (MIS) applications

Deposition velocity of gaseous organic iodine from the atmosphere to rice plants

International Nuclear Information System (INIS)

Muramatsu, Yasuyuki; Shigeo-Uchida; Sumiya, Misako; Ohmomo, Yoichiro

1996-01-01

To obtain parameter values for the assessment of 129 I transfer from the atmosphere to rice, deposition of CH 3 I to rice plants has been studied. The mass normalized deposition velocity (V D ) of CH 3 I for rough (unhulled) rice was 0.00048 cm 3 g -1 s -1 , which is about 1/300 of that of I 2 . Translocation of iodine, deposited as CH 3 I on leaves and stems, to rice grain was negligibly small. Distribution of iodine between hull and inner part of the grain was found to depend also on the chemical forms of atmospheric iodine to be deposited. The ratio of the iodine distribution in a grain exposed to CH 3 I was as follows: rough rice: brown rice (hulled rice):polished rice = 1.0:0.49:0.38. The distribution ratio in polished grains for CH 3 I exposed rice was about 20 times higher than that for I 2 . 22 refs., 1 fig., 6 tabs

Heavy metals in bark of Pinus massoniana (Lamb.) as an indicator of atmospheric deposition near a smeltery at Qujiang, China.

Science.gov (United States)

Kuang, Yuan Wen; Zhou, Guo Yi; Da Wen, Zhi; Liu, Shi Zhong

2007-06-01

Rapid urbanization and the expansion of industrial activities in the past several decades have led to large increases in emissions of pollutants in the Pearl River Delta of south China. Recent reports have suggested that industrial emission is a major factor contributing to the damages in current natural ecosystem in the Delta area. Tree barks have been used successfully to monitor the levels of atmospheric metal deposition in many areas, but rarely in China. This study aimed at determining whether atmospheric heavy metal deposition from a Pb-Zn smeltery at Qujiang, Guangdong province, could be accurately reflected both in the inner bark and the outer bark of Masson pine (Pinus massoniana L.). The impact of the emission from smeltery on the soils beneath the trees and the relationships of the concentrations between the soils and the barks were also analyzed. Barks around the bole of Pinus massoniana from a pine forest near a Pb-Zn smeltery at Qujiang and a reference forest at Dinghushan natural reserve were sampled with a stainless knife at an average height of 1.5 m above the ground. Mosses and lichens on the surface barks were cleaned prior to sampling. The samples were carefully divided into the inner bark (living part) and the outer bark (dead part) in the laboratory, and dried and ground, respectively. After being dry-ashed, the powder of the barks was dissolved in HNO3. The solutions were analyzed for iron (Fe), manganese (Mn), copper (Cu), zinc (Zn), chromium (Cr), nickel (Ni) and cobalt (Co) by inductively coupled plasmas emission spectrometry (ICP, PS-1000AT, USA) and Cadmium (Cd) and lead (Pb) by graphite furnace atomic absorption spectrometry (GFAAS, ZEENIT 60, Germany). Surface soils (0-10 cm) beneath the sample trees were also collected and analyzed for the selected metals. Concentrations of the selected metals in soils at Qujiang were far above their environmental background values in the area, except for Fe and Mn, whilst at Dinghushan, they were far

Atmospheric mercury in Changbai Mountain area, northeastern China II. The distribution of reactive gaseous mercury and particulate mercury and mercury deposition fluxes.

Science.gov (United States)

Wan, Qi; Feng, Xinbin; Lu, Julia; Zheng, Wei; Song, Xinjie; Li, Ping; Han, Shijie; Xu, Hao

2009-08-01

Reactive gaseous mercury (RGM) and particulate mercury (Hgp) concentrations in ambient air from a remote site at Changbai Mountain area in northeastern China were intermittently monitored from August 2005 to July 2006 totaling 93 days representing fall, winter-spring and summer season, respectively. Rainwater and snow samples were collected during a whole year, and total mercury (THg) in rain samples were used to calculate wet depositional flux. A throughfall method and a model method were used to estimate dry depositional flux. Results showed mean concentrations of RGM and Hgp are 65 and 77 pg m(-3). Compared to background concentrations of atmospheric mercury species in Northern Hemisphere, RGM and Hgp are significantly elevated in Changbai area. Large values for standard deviation indicated fast reactivity and a low residence time for these mercury species. Seasonal variability is also important, with lower mercury levels in summer compared to other seasons, which is attributed to scavenging by rainfall and low local mercury emissions in summer. THg concentrations ranged from 11.5 to 15.9 ng L(-1) in rainwater samples and 14.9-18.6 ng L(-1) in throughfall samples. Wet depositional flux in Changbai area is calculated to be 8.4 microg m(-2) a(-1), and dry deposition flux is estimated to be 16.5 microg m(-2) a(-1) according to a throughfall method and 20.2 microg m(-2) a(-1) using a model method.

Differences in the dry deposition of gaseous elemental I-131 to several leafy vegetable species

International Nuclear Information System (INIS)

Shinonaga, T.; Heuberger, H.; Tschiersch, J.

2004-01-01

The height of the dry deposition of gaseous elemental 131 I to leafy vegetable is quite uncertain because of the different habit, surface texture and leaf uptake of the different plant species. There is no comparative data on the deposition to various species, but leafy vegetables are taken as reference plants for the estimation of the height of contamination of vegetable foods after a nuclear accident. Therefore new chamber experiments were performed to determine under homogeneous and controlled conditions the dry deposition of gaseous elemental 131 I on mature leafy vegetable. The simultaneous exposition of endive, head lettuce, red oak leaf lettuce and spinach (spring leafy vegetable) rsp. curly kale, white cabbage and spinach (summer leafy vegetable) was arranged. The sample collective of each species was such large that for the expected variation of the results a statistically firm analysis was possible. Significant differences were observed for the 131 I deposition on spring vegetable: the deposition on spinach was roughly 3 times that on leaf lettuce, 4 times that on endive and 9 times that on head lettuce. All summer vegetables showed differences in deposition. For Iodine, the deposition on spinach was roughly 3 times (6 times) that on curly kale and 35 times (100 times) that on white cabbage in the 2 experiments. Washing by deionised water could reduce the contamination only by about 10% for 131 I. (author)

Deposition of particle-bound radionuclides in dry weather, fog, rain and snowfall

International Nuclear Information System (INIS)

Oberschachtsiek, D.; Sparmacher, H.; Kreh, R.; Adam, M.; Fuelber, K.; Stegger, J.; Bonka, H.

1992-01-01

Radionuclides emitted from nuclear plants and installations are transported in dry weather, because of turbulences and sedimentations, to plant parts above ground and near the ground and to other areas, and deposited there. The deposited activity is proportional to the activity concentration near the deposition area. In the case of particle-bound radionuclides it depends on the aerodynamic particle diameter, surface quality and other factors. In a large number of experiments deposition velocity was measured. In fog the particles to which radionuclides are bound grow by coagulation and condensation. The aerosol size spectrum changes with increasing distance from the place of emission. The type of the fog and the form of the emitted spectrum are important factors which influence this process. With normal activity distributions as a function of the aerodynamic particle diameter, the deposition velocity increases with the distance from the place of emission, up to a final value, due to the shift of the spectrum to larger diameters. (orig.) [de

Meridional transport and deposition of atmospheric 10Be

Directory of Open Access Journals (Sweden)

J. Feichter

2009-01-01

Full Text Available 10Be concentrations measured in ice cores exhibit larger temporal variability than expected based on theoretical production calculations. To investigate whether this is due to atmospheric transport a general circulation model study is performed with the 10Be production divided into stratospheric, tropospheric tropical, tropospheric subtropical and tropospheric polar sources. A control run with present day 10Be production rate is compared with a run during a geomagnetic minimum. The present 10Be production rate is 4–5 times higher at high latitudes than in the tropics whereas during a period of no geomagnetic dipole field it is constant at all latitudes. The 10Be deposition fluxes, however, show a very similar latitudinal distribution in both the present day and the geomagnetic minimum run indicating that 10Be is well mixed in the atmosphere before its deposition. This is also confirmed by the fact that the contribution of 10Be produced in the stratosphere is dominant (55%–70% and relatively constant at all latitudes. The contribution of stratospheric 10Be is approximately 70% in Greenland and 60% in Antarctica reflecting the weaker stratosphere-troposphere air exchange in the Southern Hemisphere.

A 20-year simulated climatology of global dust aerosol deposition.

Science.gov (United States)

Zheng, Yu; Zhao, Tianliang; Che, Huizheng; Liu, Yu; Han, Yongxiang; Liu, Chong; Xiong, Jie; Liu, Jianhui; Zhou, Yike

2016-07-01

Based on a 20-year (1991-2010) simulation of dust aerosol deposition with the global climate model CAM5.1 (Community Atmosphere Model, version 5.1), the spatial and temporal variations of dust aerosol deposition were analyzed using climate statistical methods. The results indicated that the annual amount of global dust aerosol deposition was approximately 1161±31Mt, with a decreasing trend, and its interannual variation range of 2.70% over 1991-2010. The 20-year average ratio of global dust dry to wet depositions was 1.12, with interannual variation of 2.24%, showing the quantity of dry deposition of dust aerosol was greater than dust wet deposition. High dry deposition was centered over continental deserts and surrounding regions, while wet deposition was a dominant deposition process over the North Atlantic, North Pacific and northern Indian Ocean. Furthermore, both dry and wet deposition presented a zonal distribution. To examine the regional changes of dust aerosol deposition on land and sea areas, we chose the North Atlantic, Eurasia, northern Indian Ocean, North Pacific and Australia to analyze the interannual and seasonal variations of dust deposition and dry-to-wet deposition ratio. The deposition amounts of each region showed interannual fluctuations with the largest variation range at around 26.96% in the northern Indian Ocean area, followed by the North Pacific (16.47%), Australia (9.76%), North Atlantic (9.43%) and Eurasia (6.03%). The northern Indian Ocean also had the greatest amplitude of interannual variation in dry-to-wet deposition ratio, at 22.41%, followed by the North Atlantic (9.69%), Australia (6.82%), North Pacific (6.31%) and Eurasia (4.36%). Dust aerosol presented a seasonal cycle, with typically strong deposition in spring and summer and weak deposition in autumn and winter. The dust deposition over the northern Indian Ocean exhibited the greatest seasonal change range at about 118.00%, while the North Atlantic showed the lowest seasonal

Multi-year Surface Deposition of {sup 210}Pb and {sup 210}Po at Lisbon - Atmospheric Depositions of {sup 210}Pb and {sup 210}Po in Lisbon, Portugal

Energy Technology Data Exchange (ETDEWEB)

Carvalho, Fernando P.; Oliveira, Joao M.; Alberto, G. [Instituto Superior Tecnico/ Campus Tecnologico e Nuclear, Universidade Tecnica de Lisboa, E.N. 10, 2686-953 Sacavem (Portugal)

2014-07-01

The long lived radon daughters {sup 210}Pb and {sup 210}Po were determined in samples of total atmospheric depositions obtained with surface collectors continuously operated during 5 years, near Lisbon. The average annual {sup 210}Pb flux was 66±12 Bq m{sup -2}, and the average annual {sup 210}Po flux was 8±3 Bq m{sup -2}, with an overall {sup 210}Po/{sup 210}Pb activity ratio of 0.15±0.06. Direct determination of the {sup 210}Pb atmospheric flux was compared with the {sup 210}Pb excess determined in soil surface layers along with atmospheric depositions of {sup 137}Cs. The deposition of atmospheric {sup 210}Pb was positively correlated with seasonal rainfall, while {sup 210}Po was mainly originated in soil particles re-suspension throughout the year and also in seasonal forest fires. Unusually high {sup 210}Po/{sup 210}Pb activity ratios, higher than unity, were occasionally recorded in atmospheric depositions and the sources and causes are discussed. Long time-series of {sup 210}Pb and {sup 210}Po deposition fluxes, as presented herein are useful to test and constrain parameters of the atmospheric Global Circulation Models. (authors)

Nitrogen emission and deposition budget in West and Central Africa

International Nuclear Information System (INIS)

Galy-Lacaux, C; Delon, C

2014-01-01

Atmospheric nitrogen depends on land surface exchanges of nitrogen compounds. In Sub Saharan Africa, deposition and emission fluxes of nitrogen compounds are poorly quantified, and are likely to increase in the near future due to land use change and anthropogenic pressure. This work proposes an estimate of atmospheric N compounds budget in West and Central Africa, along an ecosystem transect, from dry savanna to wet savanna and forest, for years 2000−2007. The budget may be considered as a one point in time budget, to be included in long term studies as one of the first reference point for Sub Saharan Africa. Gaseous dry deposition fluxes are estimated by considering N compounds concentrations measured in the frame of the IDAF network (IGAC/DEBITS/AFrica) at the monthly scale and modeling of deposition velocities at the IDAF sites, taking into account the bi directional exchange of ammonia. Particulate dry deposition fluxes are calculated using the same inferential method. Wet deposition fluxes are calculated from measurements of ammonium and nitrate chemical content in precipitations at the IDAF sites combined with the annual rainfall amount. In terms of emission, biogenic NO emissions are simulated at each IDAF site with a surface model coupled to an emission module elaborated from an artificial neural network equation. Ammonia emissions from volatilization are calculated from literature data on livestock quantity in each country and N content in manure. NO x and NH 3 emission from biomass burning and domestic fires are estimated from satellite data and emission factors. The total budget shows that emission sources of nitrogen compounds are in equilibrium with deposition fluxes in dry and wet savannas, with respectively 7.40 (±1.90) deposited and 9.01 (±3.44) kgN ha −1 yr −1 emitted in dry savanna, 8.38 (±2.04) kgN ha −1 yr −1 deposited and 9.60 (±0.69) kgN ha −1 yr −1 emitted in wet savanna. In forested ecosystems, the total budget is dominated

Atmospheric Spray Freeze-Drying: Numerical Modeling and Comparison With Experimental Measurements.

Science.gov (United States)

Borges Sebastião, Israel; Robinson, Thomas D; Alexeenko, Alina

2017-01-01

Atmospheric spray freeze-drying (ASFD) represents a novel approach to dry thermosensitive solutions via sublimation. Tests conducted with a second-generation ASFD equipment, developed for pharmaceutical applications, have focused initially on producing a light, fine, high-grade powder consistently and reliably. To better understand the heat and mass transfer physics and drying dynamics taking place within the ASFD chamber, 3 analytical models describing the key processes are developed and validated. First, by coupling the dynamics and heat transfer of single droplets sprayed into the chamber, the velocity, temperature, and phase change evolutions of these droplets are estimated for actual operational conditions. This model reveals that, under typical operational conditions, the sprayed droplets require less than 100 ms to freeze. Second, because understanding the heat transfer throughout the entire freeze-drying process is so important, a theoretical model is proposed to predict the time evolution of the chamber gas temperature. Finally, a drying model, calibrated with hygrometer measurements, is used to estimate the total time required to achieve a predefined final moisture content. Results from these models are compared with experimental data. Copyright © 2016 American Pharmacists Association®. Published by Elsevier Inc. All rights reserved.

Continuous wet-only and dry-only deposition measurements of {sup 137}Cs and {sup 7}Be: an indicator of their origin

Energy Technology Data Exchange (ETDEWEB)

Rosner, G.; Hoetzl, H.; Winkler, R. [GSF - Forschungszentrum fuer Umwelt und Gesundheit Neuherberg GmbH, Oberschleissheim (Germany). Inst. fuer Strahlenschutz

1996-09-01

Series of monthly values of {sup 137}Cs and {sup 7}Be wet and dry deposition were measured with a wet-only and a dry-only collector each having an area of 2.25 m{sup 2}. The results are presented for the period from November 1991 to May 1995. The behaviour of resuspended, Chernobyl-derived radiocesium is shown to be significantly different from that of cosmogenic {sup 7}Be and from that of global fallout {sup 137}Cs from nuclear weapons testing. The dry-to-total ratio of 0.65, the dry deposition velocity of 1.5 cm s{sup -1}, the close correlation to the total amount of solids collected and the absence of a correlation between activity deposition and amount of rainfall point to a strong similarity in the deposition behaviour of present radiocesium and that of stable elements of terrestrial origin. (author).

Changes in the atmospheric deposition of minor and rare elements between 1975 and 2000 in south Sweden, as measured by moss analysis

International Nuclear Information System (INIS)

Ruehling, Aake; Tyler, Germund

2004-01-01

Elements emitted to the atmosphere are partly exported to more remote areas and contribute to the regional and territorial deposition rates. This study is based on the principle that carpet-forming bryophytes (pleurocarpic mosses) absorb elements and particles from rain, melting snow and dry deposition. We compare the concentrations of 60 elements in carpets of the forest moss Pleurozium schreberi sampled in 1975 and 2000 within a sparsely inhabited area dominated by forest and bogland in south Sweden. As an average for all the 60 elements, the median concentration was 2.7 times higher in 1975 than in 2000. The greatest difference was measured for Pb, although In, Bi, Ge, V, Sn, As and Ag had more than 5 times higher concentrations in 1975 than in 2000. Somewhat lower 1975/2000 concentration ratios (3.0-3.8) were measured for U, Sb, Cd, W, Ga, Fe, Li, and Be. The rare-earth elements (Y, La, Ce, Pr, Nd, Sm, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu), except Eu as well as Th, Ni, Al, Ti, Hf, Nb, and Zr, had concentration ratios around the average (2.5-2.8). Possible causes of these changes are discussed. We conclude that reductions in anthropogenic dust emissions during recent decades have decreased the atmospheric deposition over northern Europe of most elements in the periodical system, as previously reported for a limited number of transition and heavy metals. Changes in the deposition of soil dust would be of minor importance to the decreased deposition rates

Changes in the atmospheric deposition of minor and rare elements between 1975 and 2000 in south Sweden, as measured by moss analysis.

Science.gov (United States)

Rühling, Ake; Tyler, Germund

2004-10-01

Elements emitted to the atmosphere are partly exported to more remote areas and contribute to the regional and territorial deposition rates. This study is based on the principle that carpet-forming bryophytes (pleurocarpic mosses) absorb elements and particles from rain, melting snow and dry deposition. We compare the concentrations of 60 elements in carpets of the forest moss Pleurozium schreberi sampled in 1975 and 2000 within a sparsely inhabited area dominated by forest and bogland in south Sweden. As an average for all the 60 elements, the median concentration was 2.7 times higher in 1975 than in 2000. The greatest difference was measured for Pb, although In, Bi, Ge, V, Sn, As and Ag had more than 5 times higher concentrations in 1975 than in 2000. Somewhat lower 1975/2000 concentration ratios (3.0-3.8) were measured for U, Sb, Cd, W, Ga, Fe, Li, and Be. The rare-earth elements (Y, La, Ce, Pr, Nd, Sm, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu), except Eu as well as Th, Ni, Al, Ti, Hf, Nb, and Zr, had concentration ratios around the average (2.5-2.8). Possible causes of these changes are discussed. We conclude that reductions in anthropogenic dust emissions during recent decades have decreased the atmospheric deposition over northern Europe of most elements in the periodical system, as previously reported for a limited number of transition and heavy metals. Changes in the deposition of soil dust would be of minor importance to the decreased deposition rates.

Shifts in lake N: P stoichiometry and nutrient limitation driven by atmospheric nitrogen deposition

Science.gov (United States)

Elser, J.J.; Andersen, T.; Baron, Jill S.; Bergstrom, A.-K.; Jansson, M.; Kyle, M.; Nydick, K.R.; Steger, L.; Hessen, D.O.

2009-01-01

Human activities have more than doubled the amount of nitrogen (N) circulating in the biosphere. One major pathway of this anthropogenic N input into ecosystems has been increased regional deposition from the atmosphere. Here we show that atmospheric N deposition increased the stoichiometric ratio of N and phosphorus (P) in lakes in Norway, Sweden, and Colorado, United States, and, as a result, patterns of ecological nutrient limitation were shifted. Under low N deposition, phytoplankton growth is generally N-limited; however, in high-N deposition lakes, phytoplankton growth is consistently P-limited. Continued anthropogenic amplification of the global N cycle will further alter ecological processes, such as biogeochemical cycling, trophic dynamics, and biological diversity, in the world's lakes, even in lakes far from direct human disturbance.

Modeling of air pollutant removal by dry deposition to urban trees using a WRF/CMAQ/i-Tree Eco coupled system

Science.gov (United States)

Maria Theresa I. Cabaraban; Charles N. Kroll; Satoshi Hirabayashi; David J. Nowak

2013-01-01

A distributed adaptation of i-Tree Eco was used to simulate dry deposition in an urban area. This investigation focused on the effects of varying temperature, LAI, and NO2 concentration inputs on estimated NO2 dry deposition to trees in Baltimore, MD. A coupled modeling system is described, wherein WRF provided temperature...

Radionuclide ratios in wet and dry deposition samples from June 1976 through December 1977

International Nuclear Information System (INIS)

Gavini, M.B.

1978-01-01

238 Pu, 239 Pu and 137 Cs in rain and dry fallout and 90 Sr in rain samples were measured at Woods Hole, Massachusetts, from June 1976 through December 1977. The dry fallout was estimated to be about 7.8% of the total deposition of 239 Pu and 137 Cs. 239 Pu/ 137 Cs ratios, almost constant at about 0.011 in rain or dry fallout, February through December 1977, suggested that fractionation between the refractory and volatile radionuclides is insignificant in stratospheric fallout. This supports the idea of regional homogeneity of radionuclide ratios in fallout. (Auth.)

Seasonal atmospheric deposition and air-sea gaseous exchange of polycyclic aromatic hydrocarbons over the Yangtze River Estuary, East China Sea: Implication for the source-sink processes

Science.gov (United States)

Jiang, Y.; Guo, Z.

2017-12-01

As the home of the largest port in the world, the Yangtze River Estuary (YRE) in the East China Sea (ECS) is adjacent to the largest economic zone in China with more than 10% of Chinese population and provides one-fifth of national GDP. The YRE is under the path of contaminated East Asian continental outflow. These make the YRE unique for the pollutant biogeochemical cycling in the world. In this work, 94 pairs of air samples and 20 surface seawater samples covering four seasons were collected from a remote receptor site in the YRE from March 2014 to January 2015, in order to explore the seasonal fluxes of air-sea gaseous exchange and atmospheric dry and wet deposition of 15 polycyclic aromatic hydrocarbons (PAHs) and their source-sink processes at the air-sea interface. The average dry and wet deposition fluxes of 15 PAHs were estimated as 879 ± 1393 ng m-2 d-1 and 755 ± 545 ng m-2 d-1, respectively. The gaseous PAHs were released from seawater to atmosphere during the whole year with an average of 3039 ± 2030 ng m-2 d-1. The gaseous exchange of PAHs was referred as the dominant process at the air-sea interface in the YRE as the magnitude of volatilization flux of PAHs exceeded that of the total dry and wet deposition. The gaseous PAH exchange flux was dominated by 3-ring PAHs, with the highest value in summer while lowest in winter, depicting a strong seasonal variation due to temperature, wind speed and air-sea concentration gradient difference among seasons. Based on the simplified mass balance estimation, net 9.6 tons/y of PAHs was volatilized from seawater to atmosphere with an area of approximately 20000 km2 in the YRE. Apart from Yangtze River input and ocean ship emissions in the entire year, the selective release of low molecular weight PAHs from sediments in winter due to re-suspension triggered by the East Asian winter monsoon could be another possible source for dissolved PAHs. This work suggests that the source-sink processes of PAHs at air

Direct dry transfer of chemical vapor deposition graphene to polymeric substrates

OpenAIRE

Fechine, Guilhermino J. M.; Martin-Fernandez, Inigo; Yiapanis, George; de Oliveira, Ricardo V. Bof; Hu, Xiao; Yarovsky, Irene; Neto, Antonio H. Castro; Ozyilmaz, Barbaros

2014-01-01

We demonstrate the direct dry transfer of large area Chemical Vapor Deposition graphene to several polymers (low density polyethylene, high density polyethylene, polystyrene, polylactide acid and poly(vinylidenefluoride-co-trifluoroethylene) by means of only moderate heat and pressure, and the later mechanical peeling of the original graphene substrate. Simulations of the graphene-polymer interactions, rheological tests and graphene transfer at various experimental conditions show that contro...

An enhanced approach for the use of satellite-derived leaf area index values in dry deposition modeling in the Athabasca oil sands region.

Science.gov (United States)

Davies, Mervyn; Cho, Sunny; Spink, David; Pauls, Ron; Desilets, Michael; Shen, Yan; Bajwa, Kanwardeep; Person, Reid

2016-12-15

In the Athabasca oil sands region (AOSR) of Northern Alberta, the dry deposition of sulphur and nitrogen compounds represents a major fraction of total (wet plus dry) deposition due to oil sands emissions. The leaf area index (LAI) is a critical parameter that affects the dry deposition of these gaseous and particulate compounds to the surrounding boreal forest canopy. For this study, LAI values based on Moderate Resolution Imaging Spectroradiometer satellite imagery were obtained and compared to ground-based measurements, and two limitations with the satellite data were identified. The satellite LAI data firstly represents one-sided LAI values that do not account for the enhanced LAI associated with needle leaf geometry, and secondly, underestimates LAI in winter-time northern latitude regions. An approach for adjusting satellite LAI values for different boreal forest cover types, as a function of time of year, was developed to produce more representative LAI values that can be used by air quality sulphur and nitrogen deposition models. The application of the approach increases the AOSR average LAI for January from 0.19 to 1.40, which represents an increase of 637%. Based on the application of the CALMET/CALPUFF model system, this increases the predicted regional average dry deposition of sulphur and nitrogen compounds for January by factors of 1.40 to 1.30, respectively. The corresponding AOSR average LAI for July increased from 2.8 to 4.0, which represents an increase of 43%. This increases the predicted regional average dry deposition of sulphur and nitrogen compounds for July by factors of 1.28 to 1.22, respectively. These findings reinforce the importance of the LAI metric for predicting the dry deposition of sulphur and nitrogen compounds. While satellite data can provide enhanced spatial and temporal resolution, adjustments are identified to overcome associated limitations. This work is considered to have application for other deposition model studies where

Detailed source term estimation of the atmospheric release for the Fukushima Daiichi Nuclear Power Station accident by coupling simulations of atmospheric dispersion model with improved deposition scheme and oceanic dispersion model

Science.gov (United States)

Katata, G.; Chino, M.; Kobayashi, T.; Terada, H.; Ota, M.; Nagai, H.; Kajino, M.; Draxler, R.; Hort, M. C.; Malo, A.; Torii, T.; Sanada, Y.

2014-06-01

Temporal variations in the amount of radionuclides released into the atmosphere during the Fukushima Dai-ichi Nuclear Power Station (FNPS1) accident and their atmospheric and marine dispersion are essential to evaluate the environmental impacts and resultant radiological doses to the public. In this paper, we estimate a detailed time trend of atmospheric releases during the accident by combining environmental monitoring data with atmospheric model simulations from WSPEEDI-II (Worldwide version of System for Prediction of Environmental Emergency Dose Information), and simulations from the oceanic dispersion model SEA-GEARN-FDM, both developed by the authors. A sophisticated deposition scheme, which deals with dry and fogwater depositions, cloud condensation nuclei (CCN) activation and subsequent wet scavenging due to mixed-phase cloud microphysics (in-cloud scavenging) for radioactive iodine gas (I2 and CH3I) and other particles (CsI, Cs, and Te), was incorporated into WSPEEDI-II to improve the surface deposition calculations. The fallout to the ocean surface calculated by WSPEEDI-II was used as input data for the SEA-GEARN-FDM calculations. Reverse and inverse source-term estimation methods based on coupling the simulations from both models was adopted using air dose rates and concentrations, and sea surface concentrations. The results revealed that the major releases of radionuclides due to FNPS1 accident occurred in the following periods during March 2011: the afternoon of 12 March due to the wet venting and hydrogen explosion at Unit 1, the morning of 13 March after the venting event at Unit 3, midnight of 14 March when the SRV (Safely Relief Valve) at Unit 2 was opened three times, the morning and night of 15 March, and the morning of 16 March. According to the simulation results, the highest radioactive contamination areas around FNPS1 were created from 15 to 16 March by complicated interactions among rainfall, plume movements, and the temporal variation of

The Use of Biomonitors to Monitor Atmospheric Deposition of 210Pb

International Nuclear Information System (INIS)

Jeran, Z.; Jacimovic, R.

1998-01-01

The main source of 210 Pb in the environment is the exhalation of 222 Rn gas from the ground to the atmosphere during the radioactive decay of natural uranium - radium chain. In the atmosphere this radionuclide is rapidly attached to small particles - aerosols, predominantly on those particles below 0.3 mm. The half-life of 210 Pb is longer than the atmospheric residence time of the aerosols on which it resides (1). By sedimentation and washout of aerosols this nuclide is then transferred to the soil or vegetation. The other main sources include burning of fossil fuels and phosphate fertilizers. The usual way to determine the levels of 210 Pb and other radionuclides in the atmosphere is the use of a high volume filter system, which should operate for a long time to collect enough material for analysis. An other approach to determining the outdoor levels of radionuclides is the use of suitable biomonitors such as lichens or mosses. These organisms, although neither evolutionarie nor taxonomically related, have some common characteristics which enable them to be used as monitors for atmospheric pollution. They lack roots and protective organs against the substances derived from the atmosphere (stomata and cuticle) and are very efficient accumulators of atmospheric particulate material and chemical substances such as radionuclides or heavy metals (2). The levels of these substances in lichens and mosses are usually much higher than in air particulates or precipitation and for these reason the analysis is much easier. Another advantage of biomonitors over conventional sampling of air particulates or precipitation is that the collection of lichens or mosses is very cheap therefore allows a very large number of sites to be included in the same survey and permits detailed geographical deposition patterns to be drawn (3). It must be emphasised that concentration data on elements or radionuclides in lichens or mosses represent the relative deposition patterns over a certain

Atmospheric corrosion tests along the Norwegian-Russian border. Part II

Energy Technology Data Exchange (ETDEWEB)

Henriksen, J.F.; Mikhailov, A.A.

1997-12-31

A bilateral exposure programme was carried out along the Norwegian-Russian border in 1990-1991, 1992-1993 and 1993-1994 to evaluate quantitatively the effect of sulphur pollutants on the atmospheric corrosion of important materials in sub-arctic climate. The first part of the programme demonstrated that also in subarctic climate do metals corrode depending on the atmospheric corrosivity, and dose-response functions were derived which combined the effects of SO{sub 2} and time of wetness. The second part of the programme, which is described in this report, involved exposures of carbon steel, zinc and copper at two sites in Norway and three sites in Russia. It is concluded that the accelerated atmospheric corrosion of metals in regions along the border is mainly due to dry deposition of sulphur. At some sites, dry deposition of Cl contributes because of sea-salt aerosols. The corrosivity of acid precipitation is certain but could not be represented as a function because of the small differences observed in the pH values at the different sites. At all test sites the kinetics of corrosion of steel, zinc and copper are characterized by a reduced corrosion rate after one year of exposure. Time of wetness is an important parameter in predicting atmospheric corrosion of metals even on a regional scale. Hence, for monitoring and for trend-effect analysis, it is very important to determine the corrosivity of SO{sub 2} with time of wetness. In accordance with dose-response functions obtained, the yearly corrosion rate for steel and zinc are higher for the areas with higher amounts of dry deposition of Cl than for areas with analogous but only SO{sub 2}-containing atmosphere. 6 refs., 8 figs., 15 tabs.

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

Directory of Open Access Journals (Sweden)

C. Knote

2015-01-01

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

Atmospheric deposition and canopy exchange processes in alpine forest ecosystems (northern Italy)

Energy Technology Data Exchange (ETDEWEB)

Balestrini, R. [Water Research Institute, Brugherio (Italy); Tagliaferri, A. [Regional Forestry Board (Italy)

2001-07-01

Throughfall and bulk precipitation chemistry were studied for five years (June 1994-May 1999) at two high elevation forest sites (Val Gerola and Val Masino) which were known to differ in terms of tree health, as assessed by live crown condition. The ion concentration of bulk precipitation samples did not differ significantly between sites, except for Mg{sup 2+}, while the throughfall concentrations differed in the measured values of H{sup +}, N-NO{sub 3}{sup -}, Cl{sup -}, Na{sup +}, K{sup +}, DOC and weak organic acids. The results of the application of the canopy exchange model indicated a higher contribution from the dry deposition of N-NO{sub 3}{sup -}, N-NH{sub 4}{sup +} and H{sup +} at Val Gerola, where the damage symptoms were more evident. In addition, the canopy leaching of Ca{sup 2+}, K{sup +} and weak organic acids were 47%, 21% and 27% higher at Val Gerola than at Val Masino. Annual SO{sub 4}{sup 2-} deposition fluxes (21.3kg ha{sup -1}yr{sup -1} at Val Masino and 23.6kgha{sup -1}yr{sup -1} at Val Gerola) were similar to those reported for moderately polluted European and U.S. sites. Annual N loads were 13.6 and 13.1kgha{sup -1}yr{sup -1} in the bulk input, and 15.0 and 18.0kgha{sup -1}yr{sup -1} in throughfall inputs, at Val Masino and Val Gerola, respectively. The contribution of the organic fraction to the total N atmospheric deposition load is significant, constituting 17% of the bulk flux and 40% of the throughfall flux. Measured nitrogen loads exceed the critical nutrient loads by several kgNha{sup -1} at both stations. In particular the nitrogen throughfall load at Val Gerola was about 3 times higher than the critical values. (author)

GCM simulations of cold dry Snowball Earth atmospheres

Science.gov (United States)

Voigt, A.; Held, I.; Marotzke, J.

2009-12-01

We use the full-physics atmospheric general circulation model ECHAM5 to investigate cold and virtually dry Snowball Earth atmospheres. These result from specifying sea ice as the surface boundary condition everywhere, corresponding to a frozen aquaplanet, while keeping total solar irradiance at its present-day value of 1365 Wm-2 and setting atmospheric carbon dioxide to 300 ppmv. Here, we present four simulations corresponding to the four possible combinations of enabled or disabled diurnal and seasonal cycles. The aim of this study is twofold. First, we focus on the zonal-mean circulation of Snowball Earth atmospheres, which, due to missing moisture, might constitute an ideal though yet unexplored testbed for theories of atmospheric dynamics. Second, we investigate tropical surface temperatures with an emphasis on the impact of the diurnal and seasonal cycles. This will indicate whether the presence of the diurnal or seasonal cycle would facilitate or anticipate the escape from Snowball Earth conditions when total solar irradiance or atmospheric CO2 levels were increased. The dynamics of the tropical circulation in Snowball Earth atmospheres differs substantially from that in the modern atmosphere. The analysis of the mean zonal momentum budget reveals that the mean flow meridional advection of absolute vorticity is primarily balanced by vertical diffusion of zonal momentum. The contribution of eddies is found to be even smaller than the contribution of mean flow vertical advection of zonal momentum, the latter being usually neglected in theories for the Hadley circulation, at least in its upper tropospheric branch. Suppressing vertical diffusion of horizontal momentum above 850 hPa leads to a stronger Hadley circulation. This behaviour cannot be understood from axisymmetric models of the atmosphere, nor idealized atmospheric general circulation models, which both predict a weakening of the Hadley circulation when the vertical viscosity is decreased globally. We

Atmospheric deposition patterns of (210)Pb and (7)Be in Cienfuegos, Cuba.

Science.gov (United States)

Alonso-Hernández, Carlos M; Morera-Gómez, Yasser; Cartas-Águila, Héctor; Guillén-Arruebarrena, Aniel

2014-12-01

The radiometric composition of bulk deposition samples, collected monthly for one year, February 2010 until January 2011, at a site located in Cienfuegos (22° 03' N, 80° 29' W) (Cuba), are analysed in this paper. Measurement of (7)Be and (210)Pb activity concentrations were carried out in 12 bulk deposition samples. The atmospheric deposition fluxes of (7)Be and (210)Pb are in the range of 13.2-132 and 1.24-8.29 Bq m(-2), and their mean values are: 56.6 and 3.97 Bq m(-2), respectively. The time variations of the different radionuclide have been discussed in relation with meteorological factors and the mean values have been compared to those published in recent literature from other sites located at different latitudes. The annual average flux of (210)Pb and (7)Be were 47 and 700 Bq m(-2) y(-1), respectively. Observed seasonal variations of deposition data are explained in terms of different environmental features. The atmospheric deposition fluxes of (7)Be and (210)Pb were moderately well correlated with precipitation and well correlated with one another. The (210)Pb/(7)Be ratios in the monthly depositions samples varied in the range of 0.05-0.10 and showed a strong correlation with the number of rainy days. Copyright © 2014 Elsevier Ltd. All rights reserved.

Evidence for the Importance of Atmospheric Nitrogen Deposition to Eutrophic Lake Dianchi, China

Science.gov (United States)

Zhan, X.; Bo, Y.; Zhou, F.; Liu, X.; Paerl, H. W.; Shen, J.; Wang, R.; Li, F. R.; Tao, S.; Yanjun, D.; Tang, X.

2017-12-01

Elevated atmospheric nitrogen (N) deposition has significantly influenced aquatic ecosystems, especially with regard to their N budgets and phytoplankton growth potentials. Compared to a considerable number of studies on oligotrophic lakes and oceanic waters, little evidence for the importance of N deposition has been generated for eutrophic lakes, even though emphasis has been placed on reducing external N inputs to control eutrophication in these lakes. Our high-resolution observations of atmospheric depositions and riverine inputs of biologically reactive N species into eutrophic Lake Dianchi (the sixth largest freshwater lake in China) shed new light onto the contribution of N deposition to total N loads. Annual N deposition accounted for 15.7% to 16.6% of total N loads under variable precipitation conditions, 2-fold higher than previous estimates (7.6%) for the Lake Dianchi. The proportion of N deposition to total N loads further increased to 27-48% in May and June when toxic blooms of the ubiquitous non-N2 fixing cyanobacteria Microcystis spp. are initiated and proliferate. Our observations reveal that reduced N (59%) contributes a greater amount than oxidized N to total N deposition, reaching 56-83% from late spring to summer. Progress toward mitigating eutrophication in Lake Dianchi and other bloom-impacted eutrophic lakes will be difficult without reductions in ammonia emissions and subsequent N deposition.

Atmospheric deposition of nutrients to north Florida rivers: A multivariate statistical analysis. Final report. Master's thesis

International Nuclear Information System (INIS)

Fu, J.

1991-01-01

Atmospheric nutrient input to the Apalachicola Bay estuary was studied because it has been demonstrated that atmospheric deposition can be a major source of nutrients to eastern U.S. estuaries. Besides the Apalachicola River, the Sopchoppy and the Ochlockonee were also selected for a comparative analysis. Receptor model, absolute principal of component analysis (APCA), and mass balance methods were applied in the study. The results of the study show that nitrogen is probably not a limiting nutrient in the three rivers because their N:P mole ratios are nearly 3 times higher than the Redfield ratio for photosynthesis. The total atmospheric nitrogen depositions in the three river watershed are at least as great as their river fluxes. In the Apalachicola River, the atmospheric source of nitrogen is found to be several times higher than the largest possible input of urban sewage. Atmospheric deposition, therefore, might be the dominant nitrogen source entering the estuary. The results of APCA show that Apalachicola River water is mainly a mixture of components that correspond in their compositions to aged rain, ground water, and fresh rain. Atmospheric nitrate deposition is the result of the air pollution, i.e., acid rain. The studies also show that the annual average deposition of nitrate has a narrow range, mainly from 5.8 to 11.5 kg/ha/yr in most of the NADP sites in the 8 southeastern states. Since all the software and data sets employed in the study are accessible nationwide, the methods could be applied in other watersheds

Atmospheric deposition of 7Be by rain events, incentral Argentina

Science.gov (United States)

Ayub, J. Juri; Di Gregorio, D. E.; Huck, H.; Velasco, H.; Rizzotto, M.

2008-08-01

Beryllium-7 is a natural radionuclide that enters into the ecosystems through wet and dry depositions and has numerous environmental applications in terrestrial and aquatic ecosystems. Atmospheric wet deposition of 7Be was measured in central Argentina. Rain traps were installed (1 m above ground) and individual rain events have been collected. Rain samples were filtered and analyzed by gamma spectrometry. The gamma counting was undertaken using a 40%-efficient p-type coaxial intrinsic high-purity natural germanium crystal built by Princeton Gamma-Tech. The cryostat was made from electroformed high-purity copper using ultralow-background technology. The detector was surrounded by 50 cm of lead bricks to provide shielding against radioactive background. The detector gamma efficiency was determined using a water solution with known amounts of chemical compounds containing long-lived naturally occurring radioisotopes, 176Lu, 138La and 40K. Due to the geometry of the sample and its position close to the detector, the efficiency points from the 176Lu decay, had to be corrected for summing effects. The measured samples were 400 ml in size and were counted curing one day. The 7Be detection limit for the present measurements was as low as 0.2 Bq l-1. Thirty two rain events were sampled and analyzed (November 2006-May 2007). The measured values show that the events corresponding to low rainfall (<20 mm) are characterized by significantly higher activity concentrations (Bq l-1). The activity concentration of each individual event varied from 0.8 to 3.5 Bq l-1, while precipitations varied between 4 and 70 mm. The integrated activity by event of 7Be was fitted with a model that takes into account the precipitation amount and the elapsed time between two rain events. The integrated activities calculated with this model show a good agreement with experimental values.

[Pollution evaluation and health risk assessment of heavy metals from atmospheric deposition in Lanzhou].

Science.gov (United States)

Li, Ping; Xue, Su-Yin; Wang, Sheng-Li; Nan, Zhong-Ren

2014-03-01

In order to evaluate the contamination and health risk of heavy metals from atmospheric deposition in Lanzhou, samples of atmospheric deposition were collected from 11 sampling sites respectively and their concentrations of heavy metals were determined. The results showed that the average contents of Cu, Pb, Cd, Cr, Ni, Zn and Mn were 82.22, 130.31, 4.34, 88.73, 40.64, 369.23 and 501.49 mg x kg(-1), respectively. There was great difference among different functional areas for all elements except Mn. According to the results, the enrichment factor score of Mn was close to 1, while the enrichment of Zn, Ni, Cu and Cr was more serious, and Pb and Cd were extremely enriched. The assessment results of geoaccumulation index of potential ecological risk indicated that the pollution of Cd in the atmospheric deposition of Lanzhou should be classified as extreme degree, and that of Cu, Ni, Zn, Pb as between slight and extreme degrees, and Cr as practically uncontaminated. Contaminations of atmospheric dust by heavy metals in October to the next March were more serious than those from April to August. Health risk assessment indicated that the heavy metals in atmospheric deposition were mainly ingested by human bodies through hand-mouth ingestion. The non-cancer risk was higher for children than for adults. The order of non-cancer hazard indexes of heavy metals was Pb > Cr > Cd > Cu > Ni > Zn. The non-cancer hazard indexes and carcinogen risks of heavy metals were both lower than their threshold values, suggesting that they will not harm the health.

Spatial patterns and temporal changes in atmospheric-mercury deposition for the midwestern USA, 2001–2016

Science.gov (United States)

Risch, Martin R.; Kenski, Donna M.

2018-01-01

Spatial patterns and temporal changes in atmospheric-mercury (Hg) deposition were examined in a five-state study area in the Midwestern USA where 32% of the stationary sources of anthropogenic Hg emissions in the continental USA were located. An extensive monitoring record for wet and dry Hg deposition was compiled for 2001–2016, including 4666 weekly precipitation samples at 13 sites and 27 annual litterfall-Hg samples at 7 sites. This study is the first to examine these Hg data for the Midwestern USA. The median annual precipitation-Hg deposition at the study sites was 10.4 micrograms per square meter per year (ug/m2/year) and ranged from 5.8 ug/m2/year to 15.0 ug/m2/year. The median annual Hg concentration was 9.4 ng/L. Annual litterfall-Hg deposition had a median of 16.1 ug/m2/year and ranged from 9.7 to 23.4 ug/m2/year. Isopleth maps of annual precipitation-Hg deposition indicated a recurring spatial pattern similar to one revealed by statistical analysis of weekly precipitation-Hg deposition. In that pattern, high Hg deposition in southeastern Indiana was present each year, frequently extending to southern Illinois. Most of central Indiana and central Illinois had similar Hg deposition. Areas with comparatively lower annual Hg deposition were observed in Michigan and Ohio for many years and frequently included part of northern Indiana. The area in southern Indiana where high Hg deposition predominated had the highest number of extreme episodes of weekly Hg deposition delivering up to 15% of the annual Hg load from precipitation in a single week. Modeled 48-h back trajectories indicated air masses for these episodes often arrived from the south and southwest, crossing numerous stationary sources of Hg emissions releasing from 23 to more than 300 kg Hg per year. This analysis suggests that local and regional, rather than exclusively continental or global Hg emissions were likely contributing to the extreme episodes and at least in part, to the spatial

Surface - atmosphere exchange of ammonia over grazed pasture

NARCIS (Netherlands)

Plantaz, M.A.H.G.

1998-01-01

This thesis deals with the exchange of ammonia between the atmosphere and grazed pasture in an area of intensive livestock breeding. The term exchange is used because gaseous ammonia can be taken up (dry deposition) as well as released (emission) by this type of surface.
Ammonia exchange

Tritium gas and tritiated water vapour behaviour in the environment from releases into the atmosphere from fusion reactors

International Nuclear Information System (INIS)

Velarde, Marta; Perlado, Manuel

2001-01-01

The diffusion of tritium from fusion reactors follows different ways according to the present chemical form, tritium gas or tritiated water vapour. The atmospheric conditions, speed and direction of the wind, rain intensity or stability class, are key factors in the dry and wet deposition. The obtained results demonstrate that the wet deposition is critical for the incorporation of the tritiated water vapour to the natural biological chain. However, the dry deposition is the factor that influences in the tritium gas form. The conversion of HT into HTO in the soil is rapid (1-7 days), and 20% of HT deposited in the soil is reemitted to the atmosphere in the form HTO, while the rest incorporates into the biological cycle. The rain factor accelerates the incorporation of tritium to the ground, the superficial waters and the underground waters

The effects of atmospheric nitrogen deposition in the Rocky Mountains of Colorado and southern Wyoming, USA-a critical review

International Nuclear Information System (INIS)

Burns, Douglas A.

2004-01-01

The Rocky Mountains of Colorado and southern Wyoming receive atmospheric nitrogen (N) deposition that ranges from 2 to 7 kg ha -1 yr -1 , and some previous research indicates pronounced ecosystem effects at the highest rates of deposition. This paper provides a critical review of previously published studies on the effects of atmospheric N deposition in the region. Plant community changes have been demonstrated through N fertilization studies, however, N limitation is still widely reported in alpine tundra and subalpine forests of the Front Range, and sensitivity to changes in snow cover alone indicate the importance of climate sensitivity in these ecosystems. Retention of N in atmospheric wet deposition is 3 - concentrations have not been demonstrated, and future trend analyses must consider the role of climate as well as N deposition. Relatively high rates of atmospheric N deposition east of the Divide may have altered nutrient limitation of phytoplankton, species composition of diatoms, and amphibian populations, but most of these effects have been inconclusive to date, and additional studies are needed to confirm hypothesized cause and effect relations. Projected future population growth and energy use in Colorado and the west increase the likelihood that the subtle effects of atmospheric N deposition now evident in the Front Range will become more pronounced and widespread in the future. - The effects of nitrogen deposition will become more evident as growth increases

Monitoring and modelling of biosphere/atmosphere exchange of gases and aerosols in Europe

Energy Technology Data Exchange (ETDEWEB)

Erisman, Jan Willem [Energy Research Centre of the Netherlands (ECN), P.O. Box 1, 1755 ZG Petten (Netherlands)]. E-mail: erisman@ecn.nl; Vermeulen, Alex [Energy Research Centre of the Netherlands (ECN), P.O. Box 1, 1755 ZG Petten (Netherlands); Hensen, Arjan [Energy Research Centre of the Netherlands (ECN), P.O. Box 1, 1755 ZG Petten (Netherlands); Flechard, Chris [Energy Research Centre of the Netherlands (ECN), P.O. Box 1, 1755 ZG Petten (Netherlands); Daemmgen, Ulrich [Federal Agricultural Research Centre, Institute of Agroecology, D-38116 Braunschweig, (Germany); Fowler, David [CEH, Bush Estate, Penicuik, Midlothian EH26 0QB (United Kingdom); Sutton, Mark [CEH, Bush Estate, Penicuik, Midlothian EH26 0QB (United Kingdom); Gruenhage, Ludger [Institute for Plant Ecology, Justus-Liebig-University, D-35392 Giessen (Germany); Tuovinen, Juha-Pekka [Finnish Meteorological Institute, FIN-00810 Helsinki (Finland)

2005-02-01

Monitoring and modelling of deposition of air pollutants is essential to develop and evaluate policies to abate the effects related to air pollution and to determine the losses of pollutants from the atmosphere. Techniques for monitoring wet deposition fluxes are widely applied. A recent intercomparison experiment, however, showed that the uncertainty in wet deposition is relatively high, up to 40%, apart from the fact that most samplers are biased because of a dry deposition contribution. Wet deposition amounts to about 80% of the total deposition in Europe with a range of 10-90% and uncertainty should therefore be decreased. During recent years the monitoring of dry deposition has become possible. Three sites have been operational for 5 years. The data are useful for model development, but also for model evaluation and monitoring of progress in policy. Data show a decline in SO{sub 2} dry deposition, whereas nitrogen deposition remained constant. Furthermore, surface affinities for pollutants changed leading to changes in deposition. Deposition models have been further developed and tested with dry deposition measurements and total deposition measurements on forests as derived from throughfall data. The comparison is reasonable given the measurement uncertainties. Progress in ozone surface exchange modelling and monitoring shows that stomatal uptake can be quantified with reasonable accuracy, but external surface uptake yields highest uncertainty. - Monitoring and modelling of the deposition of sulphur and nitrogen components and the exposure of ozone has gained much progress through the research within BIATEX.

Atmospheric nitrogen deposition: Revisiting the question of the importance of the organic component

International Nuclear Information System (INIS)

Cornell, Sarah E.

2011-01-01

The organic component of atmospheric reactive nitrogen plays a role in biogeochemical cycles, climate and ecosystems. Although its deposition has long been known to be quantitatively significant, it is not routinely assessed in deposition studies and monitoring programmes. Excluding this fraction, typically 25-35%, introduces significant uncertainty in the determination of nitrogen deposition, with implications for the critical loads approach. The last decade of rainwater studies substantially expands the worldwide dataset, giving enough global coverage for specific hypotheses to be considered about the distribution, composition, sources and effects of organic-nitrogen deposition. This data collation and meta-analysis highlights knowledge gaps, suggesting where data-gathering efforts and process studies should be focused. New analytical techniques allow long-standing conjectures about the nature and sources of organic N to be investigated, with tantalising indications of the interplay between natural and anthropogenic sources, and between the nitrogen and carbon cycles. - Highlights: → Organic-nitrogen deposition is globally ubiquitous. → Geographic patterns can now be seen in the near-global dataset. → Organic N can be formed through interactions of biogenic and anthropogenic compounds. → Neglecting organic N in deposition assessments increases critical loads uncertainty - Routinely including the organic component of atmospheric deposition (known to be around 25-35% worldwide) would make the understanding and prediction of nitrogen biogeochemistry more robust. This paper makes a preliminary global synthesis based on literature reports.

Measurement of the dry deposition flux of NH3 on to coniferous forest

NARCIS (Netherlands)

Duyzer, J.H.; Verhagen, H.L.M.; Weststrate, J.H.; Bosveld, F.C.

1992-01-01

The dry deposition flux of NH3 to coniferous forest was determined by the micrometeorological gradient method using a 36m high tower. Aerodynamic characteristics of the site were studied, using a second tower erected in the forest 100m from the first. Fluxes and gradients of heat and momentum

Model Titan atmospheric hydrocarbon analysis by Ion Mobility Spectrometry in dry helium

International Nuclear Information System (INIS)

Kojiro, D.R.; Stimac, R.M.; Wernlund, R.F.; Cohen, M.J.

1990-01-01

Ion Mobility Spectrometry (IMS) is one analytical technique being investigated for the in situ analysis of the atmosphere of Titan. Any hydrocarbon ions that may form react immediately, in microseconds, with the high concentration of water vapor normally present in conventional IMS. By reducing the water concentration to the parts-per-billion range, the lifetime of the hydrocarbon ions may be increased to the milliseconds required for measurement. At low water level concentrations, other species may become the reactant ion. This study focuses on IMS analysis of expected Titan atmospheric hydrocarbons under very dry, low water concentration conditions

Recent atmospheric lead deposition recorded in an ombrotrophic peat bog of Great Hinggan Mountains, Northeast China, from 210Pb and 137Cs dating

International Nuclear Information System (INIS)

Bao, K.; Xia, W.; Lu, X.; Wang, G.

2010-01-01

Radioactive markers are useful in dating lead deposition patterns from industrialization in peat archive. Peat cores were collected in an ombrotrophic peat bog in the Great Hinggan Mountains in Northeast China in September 2008 and dated using 210 Pb and 137 Cs radiometric techniques. The mosses in both cores were examined systematically for dry bulk density, water and ash content. Lead also was measured using atomic emission spectroscopy with inductively coupled plasma (ICP-AES). Both patterned peat profiles were preserved well without evident anthropogenic disturbance. Unsupported 210 Pb and 137 Cs decreased with the depth in both of the two sample cores. The 210 Pb chronologies were established using the constant rate of supply model (CRS) and are in good agreement with the 137 Cs time marker. Recent atmospheric 210 Pb flux in Great Hinggan Mountains peat bog was estimated to be 337 Bq m -2 y -1 , which is consistent with published data for the region. Lead deposition rate in this region was also derived from these two peat cores and ranged from 24.6 to 55.8 mg m -2 y -1 with a range of Pb concentration of 14-262 μg g -1 . The Pb deposition patterns were consistent with increasing industrialization over the last 135-170 y, with a peak of production and coal burning in the last 50 y in Northeast China. This work presents a first estimation of atmospheric Pb deposition rate in peatlands in China and suggests an increasing trend of environmental pollution due to anthropogenic contaminants in the atmosphere. More attention should be paid to current local pollution problems, and society should take actions to seek a balance between economic development and environmental protection.

Concentrations, Deposition, and Effects of Nitrogenous Pollutants in Selected California Ecosystems

Directory of Open Access Journals (Sweden)

Andrzej Bytnerowicz

2001-01-01

Full Text Available Atmospheric deposition of nitrogen (N in California ecosystems is ecologically significant and highly variable, ranging from about 1 to 45 kg/ha/year. The lowest ambient concentrations and deposition values are found in the eastern and northern parts of the Sierra Nevada Mountains and the highest in parts of the San Bernardino and San Gabriel Mountains that are most exposed to the Los Angeles air pollution plume. In the Sierra Nevada Mountains, N is deposited mostly in precipitation, although dry deposition may also provide substantial amounts of N. On the western slopes of the Sierra Nevada, the majority of airborne N is in reduced forms as ammonia (NH3 and particulate ammonium (NH4+ from agricultural activities in the California Central Valley. In southern California, most of the N air pollution is in oxidized forms as nitrogen oxides (NOx, nitric acid (HNO3, and particulate nitrate (NO3– resulting from fossil fuel combustion and subsequent complex photochemical reactions. In southern California, dry deposition of gases and particles provides most (up to 95% of the atmospheric N to forests and other ecosystems. In the mixed-conifer forest zone, elevated deposition of N may initially benefit growth of vegetation, but chronic effects may be expressed as deterioration of forest health and sustainability. HNO3 vapor alone has a potential for toxic effects causing damage of foliar surfaces of pines and oaks. In addition, dry deposition of predominantly HNO3 has lead to changes in vegetation composition and contamination of ground- and stream water where terrestrial N loading is high. Long-term, complex interactions between N deposition and other environmental stresses such as elevated ozone (O3, drought, insect infestations, fire suppression, or intensive land management practices may affect water quality and sustainability of California forests and other ecosystems.

Atmospheric spatial atomic layer deposition of in-doped ZnO

NARCIS (Netherlands)

Illiberi, A.; Scherpenborg, R.; Roozeboom, F.; Poodt, P.

2014-01-01

Indium-doped zinc oxide (ZnO:In) has been grown by spatial atomic layer deposition at atmospheric pressure (spatial-ALD). Trimethyl indium (TMIn), diethyl zinc (DEZ) and deionized water have been used as In, Zn and O precursor, respectively. The metal content of the films is controlled in the range

Intra-Urban Variability in Elemental Carbon Deposition to Tree Canopies

Science.gov (United States)

Barrett, T. E.; Ponette-González, A.; Rindy, J. E.; Sheesley, R. J.

2017-12-01

Urban areas cover biomass combustion, EC is a powerful climate-forcing agent and a significant component of fine particulate matter in urban atmospheres. Thus, understanding the factors that govern EC removal in urban areas could help mitigate climate change, while improving air quality for urban residents. EC particles can be removed from the atmosphere in precipitation (wet and fog deposition) or they can settle directly onto receptor surfaces (dry deposition). Only limited measurements indicate that EC deposition is higher in urban than in rural and remote regions. However, EC deposition likely exhibits considerable intra-urban variability, with tree canopies serving as potentially important sinks for EC on the cityscape. The goal of this research is to quantify spatial variability in total (wet + dry) EC deposition to urban tree canopies in the Dallas-Fort Worth Metroplex. Using a stratified non-random sampling design, 41 oak trees (22 post oak (Quercus stellata) and 19 live oak (Quercus virginiana)) were selected near (100 m) for measurements of throughfall (water that falls from the canopy to the forest floor). Additionally, 16 bulk rainfall samplers were deployed in grassy areas with no canopy cover. Results from one rain event indicate a volume weighted mean concentration of 83 µg EC L-1 in post oak throughfall, 36 µg EC L-1 in live oak throughfall, and 4 µg EC L-1 in bulk rainfall. Total EC deposition to oak tree canopies was 2.0 ± 2.1 (SD) mg m-2 for post oak and 0.7 ± 0.3 mg m-2 for live oak. Bulk rainfall deposition was 0.08 ± 0.1 mg m-2. Our preliminary findings show that trees are effective urban air filters, removing 9-25 times more EC from the atmosphere than rainwater alone. Resolving surface controls on atmospheric EC removal is key to developing and assessing near-term climate and air quality mitigation strategies.

A field study of pollutant deposition in radiation fog

Energy Technology Data Exchange (ETDEWEB)

Waldman, J.M.; Jacob, D.J.; Munger, J.W.; Hoffman, M.R.

1986-04-01

Deposition during fog episodes can make a significant contribution to the overall flux of pollutants in certain ecosystems. Furthermore, when atmospheric stagnation prevents normal ventilation in a region, fog deposition may become the main route of pollutant removal. Fogs can consequently exert dominant control over pollutant levels in certain atmospheres. The southern San Joaquin Valley (SJV) of California is a region prone to wintertime episodes of atmospheric stagnation. These lead to elevated pollutant concentrations and/or dense, widespread fogs. Major oil-recovery operations plus widespread agricultural and livestock feeding activities are important sources of SO/sub 2/, NO/sub X/ and NH/sub 3/ in the valley. A multifaceted program of field monitoring was conducted in the SJV during the winter 1984-1985, focusing on aspects of pollutant scavenging and removal in the fog-laden atmosphere. Concentrations of major species were measured in gas, dry aerosol and fogwater phases. In addition, depositional fluxes were monitored by surrogate-surface methods. These measurements were employed to directly assess the magnitude of removal enhancement by fog.

Atmospheric gaseous elemental mercury (GEM concentrations and mercury depositions at a high-altitude mountain peak in south China

Directory of Open Access Journals (Sweden)

X. W. Fu

2010-03-01

Full Text Available China is regarded as the largest contributor of mercury (Hg to the global atmospheric Hg budget. However, concentration levels and depositions of atmospheric Hg in China are poorly known. Continuous measurements of atmospheric gaseous elemental mercury (GEM were carried out from May 2008 to May 2009 at the summit of Mt. Leigong in south China. Simultaneously, deposition fluxes of THg and MeHg in precipitation, throughfall and litterfall were also studied. Atmospheric GEM concentrations averaged 2.80±1.51 ng m⁻³, which was highly elevated compared to global background values but much lower than semi-rural and industrial/urban areas in China. Sources identification indicates that both regional industrial emissions and long range transport of Hg from central, south and southwest China were corresponded to the elevated GEM level. Seasonal and diurnal variations of GEM were observed, which reflected variations in source intensity, deposition processes and meteorological factors. Precipitation and throughfall deposition fluxes of THg and MeHg in Mt. Leigong were comparable or lower compared to those reported in Europe and North America, whereas litterfall deposition fluxes of THg and MeHg were higher compared to Europe and North America. This highlights the importance of vegetation to Hg atmospheric cycling. In th remote forest ecosystem of China, deposition of GEM via uptake of foliage followed by litterfall was very important for the depletion of atmospheric Hg. Elevated GEM level in ambient air may accelerate the foliar uptake of Hg through air which may partly explain the elevated litterfall deposition fluxes of Hg observed in Mt. Leigong.

Atmospheric deposition, retention, and stream export of dioxins and PCBs in a pristine boreal catchment

International Nuclear Information System (INIS)

Bergknut, Magnus; Laudon, Hjalmar; Jansson, Stina; Larsson, Anna; Gocht, Tilman; Wiberg, Karin

2011-01-01

The mass-balance between diffuse atmospheric deposition of organic pollutants, amount of pollutants retained by the terrestrial environment, and levels of pollutants released to surface stream waters was studied in a pristine northern boreal catchment. This was done by comparing the input of atmospheric deposition of polychlorinated dibenzo-p-dioxins and furans (PCDD/Fs) and PCBs with the amounts exported to surface waters. Two types of deposition samplers were used, equipped with a glass fibre thimble and an Amberlite sampler respectively. The measured fluxes showed clear seasonality, with most of the input and export occurring during winter and spring flood, respectively. The mass balance calculations indicates that the boreal landscape is an effective sink for PCDD/Fs and PCBs, as 96.0-99.9 % of received bulk deposition was retained, suggesting that organic pollutants will continue to impact stream water in the region for an extended period of time. - Graphical abstract: Display Omitted Highlights: → The fluxes of organic pollutants in a pristine boreal catchment were measured. → Most of the input and export occurred during winter and spring flood. → 96.0-99.9% of received bulk deposition was retained by the landscape. → Organic pollutants will impact boreal stream waters for an extended period of time. - The boreal landscape is effective in retaining diffuse atmospheric deposition of dioxins and PCBs, slowly releasing these pollutants into nearby streams.

The estimation of areas of ground that may be contaminated after an accidental release of pollutant to the atmosphere

International Nuclear Information System (INIS)

Corbett, J.O.

1979-01-01

A method is developed for calculating the area of ground contaminated above a prescribed level after an accidental release of radioactivity or any other pollutant to the atmosphere. Numerical calculations are made for a wide range of releases, atmospheric conditions and rates of wet and dry deposition. It is shown that high atmospheric stability and rain both tend to maximize the area of significant contamination for most of the plausible range of releases. However, for very large hypothetical releases, dry conditions with an unstable atmosphere spread significant contamination furthest afield. (author)

Influence of the forest canopy on total and methyl mercury deposition in the boreal forest

Science.gov (United States)

E.L. Witt; R.K. Kolka; E.A. Nater; T.R. Wickman

2009-01-01

Atmospheric mercury deposition by wet and dry processes contributes mercury to terrestrial and aquatic systems. Factors influencing the amount of mercury deposited to boreal forests were identified in this study. Throughfall and open canopy precipitation samples were collected in 2005 and 2006 using passive precipitation collectors from pristine sites located across...

Atmospheric deposition of long-lived Beta radionuclides over the territory of Bulgaria during the last decades

Energy Technology Data Exchange (ETDEWEB)

Veleva, B. [National Institute of Meteorology and Hydrology, Bulgarian Academy of Sciences, Sofia (Bulgaria)

2013-07-01

The sources of atmospheric radioactivity are discussed and compared. Radon isotopes and their daughters' dominate the natural background of beta activity in the surface air. The man-made radionuclides, much of them beta emitters, started to contaminate regionally and globally the environment after 1940's due to the atmospheric nuclear bomb tests. Additional significant sources of technogenic radionuclides in the atmosphere were nuclear accidents with pronounced examples of Chernobyl and Fukushima. The Bulgarian network for atmospheric radioactivity monitoring has been developing since 1959 in the frame of the state Hydro-meteorological service, now National Institute of Meteorology and Hydrology. It includes daily measurements of aerosol beta activity and deposition immediately and 120h after the sampling. The time and space variations of deposited beta activity, based on long term data records are presented and impact assessment of the different sources is given. The role of precipitation in deposition of radionuclides is evaluated. (author)