scholarly journals Modeling and sensitivity analysis of transport and deposition of radionuclides from the Fukushima Dai-ichi accident

2014 ◽  
Vol 14 (20) ◽  
pp. 11065-11092 ◽  
Author(s):  
X. Hu ◽  
D. Li ◽  
H. Huang ◽  
S. Shen ◽  
E. Bou-Zeid
Keyword(s):  
Size Distribution ◽  
Dry Deposition ◽  
Wet Deposition ◽  
Emission Rate ◽  
Radioactive Decay ◽  
Radioactive Isotopes ◽  
Wind Fields ◽  
Total Deposition ◽  
Horizontal Diffusion ◽  
Ground Deposition

Abstract. The atmospheric transport and ground deposition of radioactive isotopes 131I and 137Cs during and after the Fukushima Dai-ichi Nuclear Power Plant (FDNPP) accident (March 2011) are investigated using the Weather Research and Forecasting-Chemistry (WRF-Chem) model. The aim is to assess the skill of WRF in simulating these processes and the sensitivity of the model's performance to various parameterizations of unresolved physics. The WRF-Chem model is first upgraded by implementing a radioactive decay term into the advection–diffusion solver and adding three parameterizations for dry deposition and two parameterizations for wet deposition. Different microphysics and horizontal turbulent diffusion schemes are then tested for their ability to reproduce observed meteorological conditions. Subsequently, the influence of emission characteristics (including the emission rate, the gas partitioning of 131I and the size distribution of 137Cs) on the simulated transport and deposition is examined. The results show that the model can predict the wind fields and rainfall realistically and that the ground deposition of the radionuclides can also be captured reasonably well. The modeled precipitation is largely influenced by the microphysics schemes, while the influence of the horizontal diffusion schemes on the wind fields is subtle. However, the ground deposition of radionuclides is sensitive to both horizontal diffusion schemes and microphysical schemes. Wet deposition dominated over dry deposition at most of the observation stations, but not at all locations in the simulated domain. To assess the sensitivity of the total daily deposition to all of the model physics and inputs, the averaged absolute value of the difference (AAD) is proposed. Based on AAD, the total deposition is mainly influenced by the emission rate for both 131I and 137Cs; while it is not sensitive to the dry deposition parameterizations since the dry deposition is just a minor fraction of the total deposition. Moreover, for 131I, the deposition is moderately sensitive (AAD between 10 and 40% between different runs) to the microphysics schemes, the horizontal diffusion schemes, gas-partitioning and wet deposition parameterizations. For 137Cs, the deposition is very sensitive (AAD exceeding 40% between different runs) to the microphysics schemes and wet deposition parameterizations, but moderately sensitive to the horizontal diffusion schemes and the size distribution.

scholarly journals Modeling and sensitivity analysis of transport and deposition of radionuclides from the Fukushima Daiichi accident

2014 ◽  
Vol 14 (2) ◽  
pp. 2113-2173
Author(s):  
X. Hu ◽  
D. Li ◽  
H. Huang ◽  
S. Shen ◽  
E. Bou-Zeid
Keyword(s):  
Size Distribution ◽  
Dry Deposition ◽  
Wet Deposition ◽  
Nuclear Power ◽  
Emission Rate ◽  
Radioactive Decay ◽  
Radioactive Isotopes ◽  
Horizontal Diffusion ◽  
Fukushima Daiichi ◽  
Ground Deposition

Abstract. The atmospheric transport and ground deposition of radioactive isotopes 131I and 137Cs during and after the Fukushima Daiichi Nuclear Power Plant (FDNPP) accident (March 2011) are investigated using the Weather Research and Forecasting/Chemistry (WRF/Chem) model. The aim is to assess the skill of WRF in simulating these processes and the sensitivity of the model's performance to various parameterizations of unresolved physics. The WRF/Chem model is first upgraded by implementing a radioactive decay term into the advection-diffusion solver and adding three parameterizations for dry deposition and two parameterizations for wet deposition. Different microphysics and horizontal turbulent diffusion schemes are then tested for their ability to reproduce observed meteorological conditions. Subsequently, the influence on the simulated transport and deposition of the characteristics of the emission source, including the emission rate, the gas partitioning of 131I and the size distribution of 137Cs, is examined. The results show that the model can predict the wind fields and rainfall realistically. The ground deposition of the radionuclides can also potentially be captured well but it is very sensitive to the emission characterization. It is found that the total deposition is most influenced by the emission rate for both 131I and 137Cs; while it is less sensitive to the dry deposition parameterizations. Moreover, for 131I, the deposition is also sensitive to the microphysics schemes, the horizontal diffusion schemes, gas partitioning and wet deposition parameterizations; while for 137Cs, the deposition is very sensitive to the microphysics schemes and wet deposition parameterizations, and it is also sensitive to the horizontal diffusion schemes and the size distribution.

Atmospheric deposition and canopy interactions of nitrogen in forests

1993 ◽  
Vol 23 (8) ◽  
pp. 1603-1616 ◽  
Author(s):  
Gary M. Lovett ◽  
Steven E. Lindberg
Keyword(s):  
Linear Function ◽  
Dry Deposition ◽  
Wet Deposition ◽  
Particle Deposition ◽  
Cloud Water ◽  
Organic N ◽  
Total System ◽  
Inorganic N ◽  
Deposition Rates ◽  
Total Deposition

Wet deposition of nitrogen compounds was measured and dry and cloud water deposition were estimated at 11 forested sites in North America and one site in Europe. Dry deposition was a significant pathway of N input to all the forests, averaging 46% of the total deposition. At most of these sites, NH4+ was the dominant form of fixed N in the air, but HNO3 vapor dominated the dry deposition of N. Coarse-particle deposition was often important, but fine-particle deposition usually contributed only a small amount of the dry-deposited N. The deposition rates of inorganic N, which ranged between 4.8 and 27 kg N•ha−1•year−1, were generally much higher than has been reported by other studies measuring only wet or bulk deposition. The highest deposition rates were at the high-elevation sites in the southeastern and northeastern United States and much of the deposition at these sites was attributed to cloud water. Throughfall and stemflow (TF + SF) flux was also measured at all sites, and the net canopy exchange (NCE = (TF + SF)–total deposition) was found to be negative (indicating consumption of N in the canopy) for NH4+ and NO3−, and positive (indicating canopy release) for organic N. Past reports of canopy release of NO3− can probably be attributed to washoff of dry-deposited NO3− species. Consumption of inorganic N in the canopy ranged from 1 to 12 kg N•ha−1•year−1, and was highest in the spruce and spruce–fir stands. When organic N was included in the canopy N balance, the net canopy uptake of N was generally < 15% of the total system N requirement. Total N deposition was a linear function of wet deposition for low-elevation sites, and dry deposition was a linear function of the net throughfall flux for NO3−.

scholarly journals Modelling transport and deposition of caesium and iodine from the Chernobyl accident using the DREAM model

2002 ◽  
Vol 2 (5) ◽  
pp. 397-417 ◽  
Author(s):  
J. Brandt ◽  
J. H. Christensen ◽  
L. M. Frohn
Keyword(s):  
Chernobyl Accident ◽  
Dry Deposition ◽  
Wet Deposition ◽  
Statistical Tests ◽  
Model Performance ◽  
Radioactive Material ◽  
Subgrid Scale ◽  
Simple Method ◽  
Total Deposition ◽  
Cloud Scavenging

Abstract. A tracer model, DREAM (the Danish Rimpuff and Eulerian Accidental release Model), has been developed for modelling transport, dispersion and deposition (wet and dry) of radioactive material from accidental releases, as the Chernobyl accident. The model is a combination of a Lagrangian model, that includes the near source dispersion, and an Eulerian model describing the long-range transport. The performance of the transport model has previously been tested within the European Tracer Experiment, ETEX, which included transport and dispersion of an inert, non-depositing tracer from a controlled release. The focus of this paper is the model performance with respect to the total deposition of  137Cs, 134Cs and 131I from the Chernobyl accident, using different relatively simple and comprehensive parameterizations for dry- and wet deposition. The performance, compared to measurements, of using different combinations of two different wet deposition parameterizations and three different parameterizations of dry deposition has been evaluated, using different statistical tests. The best model performance, compared to measurements, is obtained when parameterizing the total deposition combined of a simple method for dry deposition and a subgrid-scale averaging scheme for wet deposition based on relative humidities. The same major conclusion is obtained for all the three different radioactive isotopes and using two different deposition measurement databases. Large differences are seen in the results obtained by using the two different parameterizations of wet deposition based on precipitation rates and relative humidities, respectively. The parameterization based on subgrid-scale averaging is, in all cases, performing better than the parameterization based on precipitation rates. This indicates that the in-cloud scavenging process is more important than the below cloud scavenging process for the submicron particles and that the precipitation rates are relatively uncertain in the meteorological model compared to the relative humidity. Relatively small differences are, however, seen in the statistical tests between the three different parameterizations of dry deposition.

scholarly journals Triple oxygen isotopes indicate urbanization affects sources of nitrate in wet and dry atmospheric deposition

2018 ◽  
Author(s):  
David M. Nelson ◽  
Urumu Tsunogai ◽  
Ding Dong ◽  
Takuya Ohyama ◽  
Daisuke D. Komatsu ◽  
...  
Keyword(s):  
Dry Deposition ◽  
Wet Deposition ◽  
Urban Environments ◽  
Rural Site ◽  
Urban Site ◽  
Peroxy Radicals ◽  
Long Distance ◽  
Wet And Dry Deposition ◽  
Atmospheric Nitrate ◽  
Nitrate Deposition

Abstract. Atmospheric nitrate deposition resulting from anthropogenic activities negatively affects human and environmental health. Identifying deposited nitrate that is produced locally vs. that originating from long-distance transport would help inform efforts to mitigate such impacts. However, distinguishing the relative transport distances of atmospheric nitrate in urban areas remains a major challenge since it may be produced locally and/or come from upwind regions. To address this uncertainty we assessed spatiotemporal variation in monthly weighted-average Δ17O and δ15N values of wet and dry nitrate deposition during one year at urban and rural sites along the western coast of the northern Japanese island of Hokkaido, downwind of the East Asian continent. Δ17O values of nitrate in wet deposition at the urban site mirrored those of wet and dry deposition at the rural site, ranging between ~ +22 and +30 ‰ with higher values during winter and lower values in summer, which suggests greater relative importance of oxidation of NO2 by O3 during winter and OH during summer. In contrast, Δ17O values of nitrate in dry deposition at the urban site were lower (+19–+25 ‰) and displayed less distinct seasonal variation. Furthermore, the difference between δ15N values of nitrate in wet and dry nitrate deposition was, on average, 3 ‰ greater at the urban than rural site, and Δ17O and δ15N values were correlated for both forms of deposition at both sites with the exception of dry deposition at the urban site. These results suggest that, relative to nitrate in wet deposition in urban environments and wet and dry deposition in rural environments, nitrate in dry deposition in urban environments forms from relatively greater oxidation of NO by peroxy radicals and/or oxidation of NO2 by OH. Given greater concentrations of peroxy radicals and OH in cities, these results imply that dry nitrate deposition results from local NOx emissions more so than wet deposition, which is transported longer distances. These results illustrate the value of stable isotope data for distinguishing the transport distances and reaction pathways of atmospheric nitrate pollution.

Dry deposition of ammonia gas drives species change faster than wet deposition of ammonium ions: evidence from a long-term field manipulation

2011 ◽  
Vol 17 (12) ◽  
pp. 3589-3607 ◽  
Author(s):  
Lucy J. Sheppard ◽  
Ian D. Leith ◽  
Toshie Mizunuma ◽  
John Neil Cape ◽  
Alan Crossley ◽  
...  
Keyword(s):  
Dry Deposition ◽  
Wet Deposition ◽  
Ammonium Ions ◽  
Ammonia Gas ◽  
Species Change ◽  
Field Manipulation ◽  
Term Field

scholarly journals Characteristics of atmospheric mercury deposition and size-fractionated particulate mercury in urban Nanjing, China

2014 ◽  
Vol 14 (5) ◽  
pp. 2233-2244 ◽  
Author(s):  
J. Zhu ◽  
T. Wang ◽  
R. Talbot ◽  
H. Mao ◽  
X. Yang ◽  
...  
Keyword(s):  
Dry Deposition ◽  
Wet Deposition ◽  
Fine Particles ◽  
Unit Area ◽  
Atmospheric Mercury ◽  
Anthropogenic Sources ◽  
Deposition Flux ◽  
Coarse Particles ◽  
Mercury Deposition ◽  
Particulate Mercury

Abstract. A comprehensive measurement study of mercury wet deposition and size-fractionated particulate mercury (HgP) concurrent with meteorological variables was conducted from June 2011 to February 2012 to evaluate the characteristics of mercury deposition and particulate mercury in urban Nanjing, China. The volume-weighted mean (VWM) concentration of mercury in rainwater was 52.9 ng L−1 with a range of 46.3–63.6 ng L−1. The wet deposition per unit area was averaged 56.5 μg m−2 over 9 months, which was lower than that in most Chinese cities, but much higher than annual deposition in urban North America and Japan. The wet deposition flux exhibited obvious seasonal variation strongly linked with the amount of precipitation. Wet deposition in summer contributed more than 80% to the total amount. A part of contribution to wet deposition of mercury from anthropogenic sources was evidenced by the association between wet deposition and sulfates, as well as nitrates in rainwater. The ions correlated most significantly with mercury were formate, calcium, and potassium, which suggested that natural sources including vegetation and resuspended soil should be considered as an important factor to affect the wet deposition of mercury in Nanjing. The average HgP concentration was 1.10 ± 0.57 ng m−3. A distinct seasonal distribution of HgP concentrations was found to be higher in winter as a result of an increase in the PM10 concentration. Overall, more than half of the HgP existed in the particle size range less than 2.1 μm. The highest concentration of HgP in coarse particles was observed in summer, while HgP in fine particles dominated in fall and winter. The size distribution of averaged mercury content in particulates was bimodal, with two peaks in the bins of < 0.7 μm and 4.7–5.8 μm. Dry deposition per unit area of HgP was estimated to be 47.2 μg m−2 using meteorological conditions and a size-resolved particle dry deposition model. This was 16.5% less than mercury wet deposition. Compared to HgP in fine particles, HgP in coarse particles contributed more to the total dry deposition due to higher deposition velocities. Negative correlation between precipitation and the HgP concentration reflected the effect of scavenging of HgP by precipitation.

scholarly journals Temporal and Spatial variation of Contribution from Ship Emissions to the concentration and deposition of air pollutants in the Baltic Sea

2016 ◽  
Author(s):  
Karin Haglund ◽  
Björn Claremar ◽  
Anna Rutgersson
Keyword(s):  
Atmospheric Deposition ◽  
Baltic Sea ◽  
Dry Deposition ◽  
Air Pollutants ◽  
Wet Deposition ◽  
Sulphur Content ◽  
The Baltic Sea ◽  
Near Surface ◽  
Baltic Sea Region ◽  
The Baltic

Abstract. The shipping sector contributes significantly to increasing emissions of air pollutants. In order to achieve sustainable shipping, primarily through new regulations and techniques, greater knowledge of dispersion and deposition of air pollutants is required. Regional model calculations of the dispersion and deposition of sulphur, nitrogen and particulate matter from the international maritime sector in the Baltic Sea and the North Sea have been made for the years 2009 to 2013. In some areas in the Baltic Sea region the contribution of sulphur dioxide, nitrogen oxide and nitrogen dioxide from international shipping represented up to 80 % of the total near surface concentration of the pollutants. Contributions from shipping of PM2,5 and PM10 were calculated to a maximum of 21 % and 13 % respectively. The contribution of wet deposition of sulphur from shipping was maximum 29 % of the total wet deposition, and for dry deposition the contribution from shipping was maximum 84 %. The highest percentage contribution of wet deposition of nitrogen from shipping reached 28 % and for dry deposition 47 %. The highest concentrations and deposition of the pollutants in the study were found near large ports and shipping lanes. High concentrations were also found over larger areas at sea and over land where many people are exposed. With enhanced regulations for sulphur content in maritime fuel, the cleaning of exhausts through scrubbers has become a possible economic solution. Wet scrubbers meet the air quality criteria but their consequences for the marine environment are largely unknown. The resulting potential of future acidification in the Baltic Sea, both from atmospheric deposition and from open-loop scrubber water along the shipping lanes, based on different assumptions about sulphur content in fuel and scrubber usage has been assessed. Shipping is expected to increase globally and in the Baltic Sea region, deposition of sulphur due to shipping will depend on traffic density, emission regulations and technology choices for the emission controls. To evaluate future changes scenarios are developed considering the amount of scrubber technology used. The increase in deposition for the different scenarios differs slightly for the basins in the Baltic Sea. The proportion of ocean acidifying sulphur from ships increases when taking scrubber water into account and the major reason to increasing acidifying nitrogen from ships are due to increasing ship traffic. This study also generates a database of scenarios for atmospheric deposition and scrubber exhaust from the period 2011 to 2050.

scholarly journals Preliminary estimation of black carbon deposition from Nepal Climate Observatory-Pyramid data and its possible impact on snow albedo changes over Himalayan glaciers during the pre-monsoon season

2010 ◽  
Vol 10 (4) ◽  
pp. 9291-9328 ◽  
Author(s):  
T. J. Yasunari ◽  
P. Bonasoni ◽  
P. Laj ◽  
K. Fujita ◽  
E. Vuillermoz ◽  
...  
Keyword(s):  
Lower Bound ◽  
Size Distribution ◽  
Black Carbon ◽  
Dry Deposition ◽  
Monsoon Season ◽  
Deposition Velocity ◽  
Himalayan Region ◽  
Snow Surface ◽  
Concentration Data ◽  
Snow Albedo

Abstract. The possible minimal range of reduction in snow surface albedo due to dry deposition of black carbon (BC) in the pre-monsoon period (March–May) was estimated as a lower bound together with the estimation of its accuracy, based on atmospheric observations at the Nepal Climate Observatory-Pyramid (NCO-P) sited at 5079 m a.s.l. in the Himalayan region. We estimated a total BC deposition rate of 2.89 μg m−2 day−1 providing a total deposition of 266 μg m−2 for March–May at the site, based on a calculation with a minimal deposition velocity of 1.0×10−4 m s−1 with atmospheric data of equivalent BC concentration. Main BC size at NCO-P site was determined as 103.1–669.8 nm by correlation analysis between equivalent BC concentration and particulate size distribution in the atmosphere. We also estimated BC deposition from the size distribution data and found that 8.7% of the estimated dry deposition corresponds to the estimated BC deposition from equivalent BC concentration data. If all the BC is deposited uniformly on the top 2-cm pure snow, the corresponding BC concentration is 26.0–68.2 μg kg−1 assuming snow density variations of 195–512 kg m−3 of Yala Glacier close to NCO-P site. Such a concentration of BC in snow could result in 2.0–5.2% albedo reductions. From a simple numerical calculations and if assuming these albedo reductions continue throughout the year, this would lead to a runoff increases of 70–204 mm of water drainage equivalent of 11.6–33.9% of the annual discharge of a typical Tibetan glacier. Our estimates of BC concentration in snow surface for pre-monsoon season can be considered comparable to those at similar altitude in the Himalayan region, where glaciers and perpetual snow region starts in the vicinity of NCO-P. Our estimates from only BC are likely to represent a lower bound for snow albedo reductions, since a fixed slower deposition velocity was used and atmospheric wind and turbulence effects, snow aging, dust deposition, and snow albedo feedbacks were not considered. This study represents the first investigation about BC deposition on snow from atmospheric aerosol data in Himalayas and related albedo effect is especially the first track at the southern slope of Himalayas.

scholarly journals Wet and dry deposition of mineral dust particles in Japan: factors related to temporal variation and spatial distribution

2013 ◽  
Vol 13 (8) ◽  
pp. 21801-21835
Author(s):  
K. Osada ◽  
S. Ura ◽  
M. Kagawa ◽  
M. Mikami ◽  
T. Y. Tanaka ◽  
...  
Keyword(s):  
Dry Deposition ◽  
Wet Deposition ◽  
Mineral Dust ◽  
Temporal Variations ◽  
Dust Particles ◽  
Insoluble Residue ◽  
Spatial Distributions ◽  
Dust Deposition ◽  
Deposition Fluxes ◽  
Deposition Amount

Abstract. Data of temporal variations and spatial distributions of mineral dust deposition fluxes are very limited in terms of duration, location, and processes of deposition. To ascertain temporal variations and spatial distributions of mineral dust deposition by wet and dry processes, weekly deposition samples were obtained at Sapporo, Toyama, Nagoya, Tottori, Fukuoka, and Cape Hedo (Okinawa) in Japan during October 2008–December 2010 using automatic wet and dry separating samplers. Mineral dust weights in water-insoluble residue were estimated from Fe contents measured using an X-ray fluorescence analyzer. For wet deposition, highest and lowest annual dust fluxes were found at Toyama (9.6 g m−2 yr−1) and at Cape Hedo (1.7 g m−2 yr−1) as average values in 2009 and 2010. Higher wet deposition fluxes were observed at Toyama and Tottori, where frequent precipitation (>60% days per month) was observed during dusty seasons. For dry deposition among Toyama, Tottori, Fukuoka, and Cape Hedo, the highest and lowest annual dust fluxes were found respectively at Fukuoka (5.2 g m−2 yr−1) and at Cape Hedo (2.0 g m−2 yr−1) as average values in 2009 and 2010. Although the seasonal tendency of the monthly dry deposition amount roughly resembled that of monthly days of Kosa dust events, the monthly amount of dry deposition was not proportional to monthly days of the events. Comparison of dry deposition fluxes with vertical distribution of dust particles deduced from Lidar data and coarse particle concentrations suggested that the maximum dust layer height or thickness is an important factor for controlling the dry deposition amount after long-range transport of dust particles. Size distributions of refractory dust particles were obtained using four-stage filtration: >20, >10, >5, and >1 μm diameter. Weight fractions of the sum of >20 μm and 10–20 μm (giant fraction) were higher than 50% for most of the event samples. Irrespective of the deposition type, the giant dust fractions were decreasing generally with increasing distance from the source area, suggesting the selective depletion of larger giant particles during atmospheric transport. Because giant dust particles are an important mass fraction of dust accumulation, especially in the north Pacific where is known as a high-nutrient, low-chlorophyll (HNLC) region, the transport height of giant dust particles is an important factor for studying dust budgets in the atmosphere and their role in biogeochemical cycles.

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