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

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.

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.

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.

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.

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)

Atmospheric wet and dry deposition of trace elements at 10 sites in Northern China

Science.gov (United States)

Pan, Y. P.; Wang, Y. S.

2015-01-01

Atmospheric deposition is considered to be a major process that removes pollutants from the atmosphere and an important source of nutrients and contaminants for ecosystems. Trace elements (TEs), especially toxic metals deposited on plants and into soil or water, can cause substantial damage to the environment and human health due to their transfer and accumulation in food chains. Despite public concerns, quantitative knowledge of metal deposition from the atmosphere to ecosystems remains scarce. To advance our understanding of the spatiotemporal variations in the magnitudes, pathways, compositions and impacts of atmospherically deposited TEs, precipitation (rain and snow) and dry-deposited particles were collected simultaneously at 10 sites in Northern China from December 2007 to November 2010. The measurements showed that the wet and dry depositions of TEs in the target areas were orders of magnitude higher than previous observations within and outside China, generating great concern over the potential risks. The spatial distribution of the total (wet plus dry) deposition flux was consistent with that of the dry deposition, with a significant decrease from industrial and urban areas to suburban, agricultural and rural sites, while the wet deposition exhibited less spatial variation. In addition, the seasonal variation of wet deposition was also different from that of dry deposition, although they were both governed by the precipitation and emission patterns. For the majority of TEs that exist as coarse particles, dry deposition dominated the total flux at each site. This was not the case for potassium, nickel, arsenic, lead, zinc, cadmium, selenium, silver and thallium, for which the relative importance between wet and dry deposition fluxes varied by site. Whether wet deposition is the major atmospheric cleansing mechanism for the TEs depends on the size distribution of the particles. We found that atmospheric inputs of copper, lead, zinc, cadmium, arsenic and

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).

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.

Atmospheric and oceanic dust fluxes in the northeastern tropical Atlantic Ocean: how close a coupling?

Directory of Open Access Journals (Sweden)

A. Bory

2002-12-01

Full Text Available Atmospheric inputs to the ocean of dust originating from Africa are compared with downward dust flux in the oceanic water column. Atmospheric fluxes were estimated using remote-sensing-derived dust optical thickness and parameters from a transport/deposition model (TM2z. Oceanic fluxes were measured directly over/in two regions of contrasting primary productivity of the northeastern tropical Atlantic (one mesotrophic and one oligotrophic, located at about 500 and 1500 km off Mauritania underlying the offshore dust plume. In both regions, estimates of annual atmospheric dust inputs to the ocean surface are lower than, but of the same order of magnitude as, oceanic fluxes (49.5 and 8.8 mg.m-2 .d-1 in the mesotrophic and oligotrophic regions. Part of this mismatch may reflect both a general flaw in the dust grain size distribution used in transport models, which likely underestimates large particles, and/or lateral advection to each region of dustier surface waters from upstream, where dust deposition is higher. Higher-frequency temporal coupling between atmospheric and oceanic fluxes seems to be primary-productivity dependent, as hypothesized in previously reported studies.Key words. Atmospheric composition and structure (aerosols and particles; geochemical cycles Oceanography: biological and chemical (geochemistry

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.

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

with these standard collectors in a region will not reduce the large uncertainty in rates derived from existing data. Calibrated surface accumulation methods hold promise as a primary means to estimate P flux in future monitoring. New methods for long-term P deposition monitoring will require an intercomparison of P flux estimates from surrogate surfaces, impactor sampling of particle concentrations combined with deposition models, and “throughfall” estimates for natural canopies. With better sampling methods and more long-term monitoring data, the importance of atmospheric P deposition in ecosystem dynamics and management can be better understood and predicted.

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 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 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.

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

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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.

Forest vegetation as a sink for atmospheric particulates: Quantitative studies in rain and dry deposition

International Nuclear Information System (INIS)

Russel, I.J.; Choquette, C.E.; Fang, S.; Dundulis, W.P.; Pao, A.A.; Pszenny, A.A.P.

1981-01-01

Radionuclides in the atmosphere are associated with nonradioactive air particulates and hence serve to trace the fluxes of air particulates to various surfaces. Natural and artificial radioactivities found in the atmosphere have been measured in vegetation for 10 years to elucidate some of the mechanisms of acquirement by forest trees of atmospheric particulates. Whole tree analysis, in conjunction with soil assay, have served to establish the fraction of the flux of radionuclides retained by above-ground tissues of a forest stand. Interpretation is facilitated because most radionuclides in the atmosphere are superficially acquired. Typically 5--20% of the total open field flux is retained by the forest canopy in a moderately rainy climate (120 cm/year). Short-lived daughters of radon give a dry deposition velocity of particulates in the Aitken size range of 0.03--0.05 cm/s, thus permitting an estimate of transient removal by forest canopies by dry deposition of this size fraction

HyFlux - Part I: Regional Modeling of Methane Flux From Near-Seafloor Gas Hydrate Deposits on Continental Margins

Science.gov (United States)

MacDonald, I. R.; Asper, V.; Garcia, O. P.; Kastner, M.; Leifer, I.; Naehr, T.; Solomon, E.; Yvon-Lewis, S.; Zimmer, B.

2008-12-01

HyFlux - Part I: Regional modeling of methane flux from near-seafloor gas hydrate deposits on continental margins MacDonald, I.R., Asper, V., Garcia, O., Kastner, M., Leifer, I., Naehr, T.H., Solomon, E., Yvon-Lewis, S., and Zimmer, B. The Dept. of Energy National Energy Technology Laboratory (DOE/NETL) has recently awarded a project entitled HyFlux: "Remote sensing and sea-truth measurements of methane flux to the atmosphere." The project will address this problem with a combined effort of satellite remote sensing and data collection at proven sites in the Gulf of Mexico where gas hydrate releases gas to the water column. Submarine gas hydrate is a large pool of greenhouse gas that may interact with the atmosphere over geologic time to affect climate cycles. In the near term, the magnitude of methane reaching the atmosphere from gas hydrate on continental margins is poorly known because 1) gas hydrate is exposed to metastable oceanic conditions in shallow, dispersed deposits that are poorly imaged by standard geophysical techniques and 2) the consumption of methane in marine sediments and in the water column is subject to uncertainty. The northern GOM is a prolific hydrocarbon province where rapid migration of oil, gases, and brines from deep subsurface petroleum reservoirs occurs through faults generated by salt tectonics. Focused expulsion of hydrocarbons is manifested at the seafloor by gas vents, gas hydrates, oil seeps, chemosynthetic biological communities, and mud volcanoes. Where hydrocarbon seeps occur in depths below the hydrate stability zone (~500m), rapid flux of gas will feed shallow deposits of gas hydrate that potentially interact with water column temperature changes; oil released from seeps forms sea-surface features that can be detected in remote-sensing images. The regional phase of the project will quantify verifiable sources of methane (and oil) the Gulf of Mexico continental margin and selected margins (e.g. Pakistan Margin, South China Sea

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....

Stomatal and Non-Stomatal Turbulent Deposition Flux of Ozone to a Managed Peatland

Directory of Open Access Journals (Sweden)

Tarek S. El-Madany

2017-09-01

Full Text Available Ozone is a key trace gas in the troposphere; because it is a greenhouse gas, it is very reactive, and it is potentially toxic to humans, fauna, and vegetation. The main sink processes for ozone are chemical reactions and the turbulent deposition flux to the earth’s surface. The deposition process itself is rather complex: The interactions between co-varying drivers such as the tropospheric ozone concentration, turbulence, and chemical reactions are not well understood. In the case of ozone deposition to vegetation, another aspect that must be studied is the role of stomatal regulation for a wide range of conditions. Therefore, we measured turbulent deposition fluxes of ozone with the eddy covariance technique during the peak of the growing season in 2014 over a managed, rewetted peatland in NW Germany. The deposition flux was large during the day (up to −15 nmol m−2 s−1 and relatively small during the night (between −1 and −2 nmol m−2 s−1. Flux partitioning by applying the surface resistance analogy and further analysis showed that the stomatal uptake was smaller than non-stomatal deposition. The correction of stomatal conductance with the gross primary production (GPP improved the estimation of day- and nighttime stomatal deposition fluxes. Statistical analysis confirmed that the friction velocity (u* was the single most important driver of non-stomatal ozone deposition and that relationships with other environmental drivers are not linear and highly variable. Further research is needed to develop a better process understanding of non-stomatal ozone deposition, to quantify the role of surface deposition to the ozone budget of the atmospheric boundary layer, and to estimate uncertainties associated with the partitioning of ozone deposition into stomatal and non-stomatal fluxes.

Determination of the Atmospheric Neutrino Fluxes from Atmospheric Neutrino Data

NARCIS (Netherlands)

Gonzalez-Garcia, M. C.; Maltoni, M.; Rojo, J.

2006-01-01

The precise knowledge of the atmospheric neutrino fluxes is a key ingredient in the interpretation of the results from any atmospheric neutrino experiment. In the standard atmospheric neutrino data analysis, these fluxes are theoretical inputs obtained from sophisticated numerical calculations based

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.

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.

[Characteristics of mercury exchange flux between soil and atmosphere under the snow retention and snow melting control].

Science.gov (United States)

Zhang, Gang; Wang, Ning; Ai, Jian-Chao; Zhang, Lei; Yang, Jing; Liu, Zi-Qi

2013-02-01

Jiapigou gold mine, located in the upper Songhua River, was once the largest mine in China due to gold output, where gold extraction with algamation was widely applied to extract gold resulting in severe mercury pollution to ambient environmental medium. In order to study the characteristics of mercury exchange flux between soil (snow) and atmosphere under the snow retention and snow melting control, sampling sites were selected in equal distances along the slope which is situated in the typical hill-valley terrain unit. Mercury exchange flux between soil (snow) and atmosphere was determined with the method of dynamic flux chamber and in all sampling sites the atmosphere concentration from 0 to 150 cm near to the earth in the vertical direction was measured. Furthermore, the impact factors including synchronous meteorology, the surface characteristics under the snow retention and snow melting control and the mercury concentration in vertical direction were also investigated. The results are as follows: During the period of snow retention and melting the air mercury tends to gather towards valley bottom along the slope and an obvious deposit tendency process was found from air to the earth's surface under the control of thermal inversion due to the underlying surface of cold source (snow surface). However, during the period of snow melting, mercury exchange flux between the soil and atmosphere on the surface of the earth with the snow being melted demonstrates alternative deposit and release processes. As for the earth with snow covered, the deposit level of mercury exchange flux between soil and atmosphere is lower than that during the period of snow retention. The relationship between mercury exchange flux and impact factors shows that in snow retention there is a remarkable negative linear correlation between mercury exchange flux and air mercury concentration as well as between the former and the air temperature. In addition, in snow melting mercury exchange

Control of Toxic Chemicals in Puget Sound, Phase 3: Study of Atmospheric Deposition of Air Toxics to the Surface of Puget Sound

Energy Technology Data Exchange (ETDEWEB)

Brandenberger, Jill M.; Louchouarn, Patrick; Kuo, Li-Jung; Crecelius, Eric A.; Cullinan, Valerie I.; Gill, Gary A.; Garland, Charity R.; Williamson, J. B.; Dhammapala, R.

2010-07-05

The results of the Phase 1 Toxics Loading study suggested that runoff from the land surface and atmospheric deposition directly to marine waters have resulted in considerable loads of contaminants to Puget Sound (Hart Crowser et al. 2007). The limited data available for atmospheric deposition fluxes throughout Puget Sound was recognized as a significant data gap. Therefore, this study provided more recent or first reported atmospheric deposition fluxes of PAHs, PBDEs, and select trace elements for Puget Sound. Samples representing bulk atmospheric deposition were collected during 2008 and 2009 at seven stations around Puget Sound spanning from Padilla Bay south to Nisqually River including Hood Canal and the Straits of Juan de Fuca. Revised annual loading estimates for atmospheric deposition to the waters of Puget Sound were calculated for each of the toxics and demonstrated an overall decrease in the atmospheric loading estimates except for polybrominated diphenyl ethers (PBDEs) and total mercury (THg). The median atmospheric deposition flux of total PBDE (7.0 ng/m2/d) was higher than that of the Hart Crowser (2007) Phase 1 estimate (2.0 ng/m2/d). The THg was not significantly different from the original estimates. The median atmospheric deposition flux for pyrogenic PAHs (34.2 ng/m2/d; without TCB) shows a relatively narrow range across all stations (interquartile range: 21.2- 61.1 ng/m2/d) and shows no influence of season. The highest median fluxes for all parameters were measured at the industrial location in Tacoma and the lowest were recorded at the rural sites in Hood Canal and Sequim Bay. Finally, a semi-quantitative apportionment study permitted a first-order characterization of source inputs to the atmosphere of the Puget Sound. Both biomarker ratios and a principal component analysis confirmed regional data from the Puget Sound and Straits of Georgia region and pointed to the predominance of biomass and fossil fuel (mostly liquid petroleum products such

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.

Deposition pattern and throughfall fluxes in secondary cool temperate forest, South Korea

Science.gov (United States)

Kumar Gautam, Mukesh; Lee, Kwang-Sik; Song, Byeong-Yeol

2017-07-01

Chemistry and deposition fluxes in the rainfall and throughfall of red pine (Pinus densiflora), black locust (Robinia pseudoacacia), and chestnut (Castanea crenata) monocultures, and mixed red pine-black locust-chestnut stands were examined in a nutrient-limited cool temperate forest of central South Korea. Throughfall was enriched in both basic and acidic constituents relative to rainfall, suggesting that both dry deposition and canopy leaching are important sources of throughfall constituents. Net throughfall fluxes (NTFs) of cations and anions significantly differed among four different stands as well as seasonally. Red pine exhibited highest fluxes (TF and NTF) for Ca2+, black locust for K+, mixed stands for Mg2+, and chestnut for Na+. In contrast, NTF of SO42-, NO3-, and NH4+was highest in the red pine, intermediate in the chestnut and mixed stands, and lowest in the black locust. In general, canopy uptake of H+ and NH4+ for all stands was higher in summer than in winter. Dry deposition appears to play a major role in atmospheric deposition to this cool temperate forest, especially in summer. Dry deposition for both cations and anions displayed high spatial variability, even though stands were adjacent to one another and experienced identical atmospheric deposition loads. Canopy leaching of K+ (95-78% of NTF), Mg2+ (92-23% of NTF), and Ca2+ (91-12% of NTF) was highest for the black locust, lowest for chestnut, and intermediate for the red pine and mixed stands. The present study documented significant changes in throughfall chemistry and NTF among different forest stands, which presumably be related with the differences in the canopy characteristics and differences in their scavenging capacity for dry deposition and canopy exchange. Difference in the canopy retention of H+ and base cation leaching suggests that canopy exchange was mainly driven by weak acid excretion and lesser by H+ exchange reaction. Our results indicate that despite a high base cation

Impact of acid atmosphere deposition on soils : field monitoring and aluminum chemistry

NARCIS (Netherlands)

Mulder, J.

1988-01-01

The effect of acid atmospheric deposition on concentrations and transfer of major solutes in acid, sandy soils was studied. Emphasis was given to mobilization and transport of potentially toxic aluminum. Data on solute concentrations and fluxes in meteoric water as well as soil solutions

Determination of the atmospheric neutrino fluxes from atmospheric neutrino data

International Nuclear Information System (INIS)

Gonzalez-Garcia, C.; Maltoni, M.; Rojo, J.

2006-06-01

The precise knowledge of the atmospheric neutrino fluxes is a key ingredient in the interpretation of the results from any atmospheric neutrino experiment. In the standard data analysis, these fluxes are theoretical inputs obtained from sophisticated numerical calculations based on the convolution of the primary cosmic ray spectrum with the expected yield of neutrinos per incident cosmic ray. In this work we present an alternative approach to the determination of the atmospheric neutrino fluxes based on the direct extraction from the experimental data on neutrino event rates. The extraction is achieved by means of a combination of artificial neural networks as interpolants and Monte Carlo methods for faithful error estimation. (author)

Determination of the atmospheric neutrino fluxes from atmospheric neutrino data

International Nuclear Information System (INIS)

Gonzalez-Garcia, Concepcion; Maltoni, Michele; Rojo, Joan

2006-01-01

The precise knowledge of the atmospheric neutrino fluxes is a key ingredient in the interpretation of the results from any atmospheric neutrino experiment. In the standard data analysis, these fluxes are theoretical inputs obtained from sophisticated numerical calculations based on the convolution of the primary cosmic ray spectrum with the expected yield of neutrinos per incident cosmic ray. In this work we present an alternative approach to the determination of the atmospheric neutrino fluxes based on the direct extraction from the experimental data on neutrino event rates. The extraction is achieved by means of a combination of artificial neural networks as interpolants and Monte Carlo methods for faithful error estimation

Atmospheric organic nitrogen deposition: analysis of nationwide data and a case study in Northeast China.

Science.gov (United States)

Jiang, C M; Yu, W T; Ma, Q; Xu, Y G; Zou, H; Zhang, S C; Sheng, W P

2013-11-01

The origin of atmospheric dissolved organic nitrogen (DON) deposition is not very clear at present. Across China, the DON deposition was substantially larger than that of world and Europe, and we found significant positive correlation between contribution of DON and the deposition flux with pristine site data lying in outlier, possibly reflecting the acute air quality problems in China. For a case study in Northeast China, we revealed the deposited DON was mainly derived from intensive agricultural activities rather than the natural sources by analyzing the compiled dataset across China and correlating DON flux with NH4(+)-N and NO3(-)-N. Crop pollens and combustion of fossil fuels for heating probably contributed to summer and autumn DON flux respectively. Overall, in Northeast China, DON deposition could exert important roles in agro-ecosystem nutrient management and carbon sequestration of natural ecosystems; nationally, it was suggested to found rational network for monitoring DON deposition. Crown Copyright © 2013. Published by Elsevier Ltd. All rights reserved.

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 FLUKA atmospheric neutrino flux calculation

CERN Document Server

Battistoni, G.; Montaruli, T.; Sala, P.R.

2003-01-01

The 3-dimensional (3-D) calculation of the atmospheric neutrino flux by means of the FLUKA Monte Carlo model is here described in all details, starting from the latest data on primary cosmic ray spectra. The importance of a 3-D calculation and of its consequences have been already debated in a previous paper. Here instead the focus is on the absolute flux. We stress the relevant aspects of the hadronic interaction model of FLUKA in the atmospheric neutrino flux calculation. This model is constructed and maintained so to provide a high degree of accuracy in the description of particle production. The accuracy achieved in the comparison with data from accelerators and cross checked with data on particle production in atmosphere certifies the reliability of shower calculation in atmosphere. The results presented here can be already used for analysis by current experiments on atmospheric neutrinos. However they represent an intermediate step towards a final release, since this calculation does not yet include the...

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 neutrino fluxes

International Nuclear Information System (INIS)

Honda, M.; Kasahara, K.; Hidaka, K.; Midorikawa, S.

1990-02-01

A detailed Monte Carlo simulation of neutrino fluxes of atmospheric origin is made taking into account the muon polarization effect on neutrinos from muon decay. We calculate the fluxes with energies above 3 MeV for future experiments. There still remains a significant discrepancy between the calculated (ν e +antiν e )/(ν μ +antiν μ ) ratio and that observed by the Kamiokande group. However, the ratio evaluated at the Frejus site shows a good agreement with the data. (author)

Five-year records of mercury wet deposition flux at GMOS sites in the Northern and Southern hemispheres

Science.gov (United States)

Sprovieri, Francesca; Pirrone, Nicola; Bencardino, Mariantonia; D'Amore, Francesco; Angot, Helene; Barbante, Carlo; Brunke, Ernst-Günther; Arcega-Cabrera, Flor; Cairns, Warren; Comero, Sara; Diéguez, María del Carmen; Dommergue, Aurélien; Ebinghaus, Ralf; Feng, Xin Bin; Fu, Xuewu; Garcia, Patricia Elizabeth; Gawlik, Bernd Manfred; Hageström, Ulla; Hansson, Katarina; Horvat, Milena; Kotnik, Jože; Labuschagne, Casper; Magand, Olivier; Martin, Lynwill; Mashyanov, Nikolay; Mkololo, Thumeka; Munthe, John; Obolkin, Vladimir; Ramirez Islas, Martha; Sena, Fabrizio; Somerset, Vernon; Spandow, Pia; Vardè, Massimiliano; Walters, Chavon; Wängberg, Ingvar; Weigelt, Andreas; Yang, Xu; Zhang, Hui

2017-02-01

The atmospheric deposition of mercury (Hg) occurs via several mechanisms, including dry and wet scavenging by precipitation events. In an effort to understand the atmospheric cycling and seasonal depositional characteristics of Hg, wet deposition samples were collected for approximately 5 years at 17 selected GMOS monitoring sites located in the Northern and Southern hemispheres in the framework of the Global Mercury Observation System (GMOS) project. Total mercury (THg) exhibited annual and seasonal patterns in Hg wet deposition samples. Interannual differences in total wet deposition are mostly linked with precipitation volume, with the greatest deposition flux occurring in the wettest years. This data set provides a new insight into baseline concentrations of THg concentrations in precipitation worldwide, particularly in regions such as the Southern Hemisphere and tropical areas where wet deposition as well as atmospheric Hg species were not investigated before, opening the way for future and additional simultaneous measurements across the GMOS network as well as new findings in future modeling studies.

Fluxes of total reactive atmospheric nitrogen (ΣNr using eddy covariance above arable land

Directory of Open Access Journals (Sweden)

Christophe R. Flechard

2013-02-01

Full Text Available The amount and timing of reactive nitrogen exchange between agricultural land and the atmosphere play a key role in evaluating ecosystem productivity and in addressing atmospheric nitrogen budgets and transport. With the recent development of the Total Reactive Atmospheric Nitrogen Converter (TRANC apparatus, a methodology has been provided for continuous measurement of the sum of all airborne nitrogen containing species (ΣNr allowing for diurnal and seasonal investigations. We present ΣNr concentration and net flux data from an 11-month field campaign conducted at an arable field using the TRANC system within an eddy-covariance setup. Clear diurnal patterns of both ΣNr concentrations and fluxes with significant dependencies on atmospheric stability and stomatal regulation were observed in the growing season. TRANC data were compared with monthly-averaged concentrations and dry deposition rates of selected Nr compounds using DELTA denuders and ensemble-averages of four inferential models, respectively. Similar seasonal trends were found for Nr concentrations from DELTA and TRANC measurements with values from the latter being considerably higher than those of DELTA denuders. The variability of the difference between these two systems could be explained by seasonally changing source locations of NOx contributions to the TRANC signal. As soil and vegetation Nr emissions to the atmosphere are generally not treated by inferential (dry deposition models, TRANC data showed lower monthly deposition rates than those obtained from inferential modelling. Net ΣNr exchange was almost neutral (~0.072 kg N ha−1 at the end of the observation period. However, during most parts of the year, slight but permanent net ΣNr deposition was found. Our measurements demonstrate that fertilizer addition followed by substantial ΣNr emissions plays a crucial role in a site's annual atmospheric nitrogen budget. As long-term Nr measurements with high temporal

Long-term atmospheric wet deposition of dissolved organic nitrogen in a typical red-soil agro-ecosystem, Southeastern China.

Science.gov (United States)

Cui, Jian; Zhou, Jing; Peng, Ying; He, Yuan Q; Yang, Hao; Xu, Liang J; Chan, Andy

2014-05-01

Dissolved organic nitrogen (DON) from atmospheric deposition has been a growing concern in the world and atmospheric nitrogen (N) deposition is increasing quickly in China especially Southeastern China. In our study, DON wet deposition was estimated by collecting and analyzing rainwater samples continuously over eight years (2005-2012) in a typical red-soil farmland ecosystem, Southeast China. Results showed that the volume-weighted-average DON concentration varied from 0.2 to 3.3 mg N L(-1) with an average of 1.2 mg N L(-1). DON flux ranged from 5.7 to 71.6 kg N ha(-1) year(-1) and averaged 19.7 kg N ha(-1) year(-1) which accounted for 34.6% of the total dissolved nitrogen (TDN) in wet deposition during the eight-year period. Analysis of DON concentration and flux, contribution of DON to TDN, rainfall, rain frequency, air temperature and wind frequency and the application of pig manure revealed possible pollution sources. Significant positive linear relation of annual DON flux and usage of pig manure (Pcycle in the red-soil agro-ecosystem in the future.

Atmospheric organic nitrogen deposition: Analysis of nationwide data and a case study in Northeast China

International Nuclear Information System (INIS)

Jiang, C.M.; Yu, W.T.; Ma, Q.; Xu, Y.G.; Zou, H.; Zhang, S.C.; Sheng, W.P.

2013-01-01

The origin of atmospheric dissolved organic nitrogen (DON) deposition is not very clear at present. Across China, the DON deposition was substantially larger than that of world and Europe, and we found significant positive correlation between contribution of DON and the deposition flux with pristine site data lying in outlier, possibly reflecting the acute air quality problems in China. For a case study in Northeast China, we revealed the deposited DON was mainly derived from intensive agricultural activities rather than the natural sources by analyzing the compiled dataset across China and correlating DON flux with NH 4 + –N and NO 3 − –N. Crop pollens and combustion of fossil fuels for heating probably contributed to summer and autumn DON flux respectively. Overall, in Northeast China, DON deposition could exert important roles in agro-ecosystem nutrient management and carbon sequestration of natural ecosystems; nationally, it was suggested to found rational network for monitoring DON deposition. -- Highlights: •Contribution and deposition flux of DON across China was positively correlated. •Deposited DON was more influenced by human in China than across the world and Europe. •DON of a farmland in Northeast China was mainly derived from agricultural activities. •Crop pollen and combustion of fossil fuels contributed to summer and autumn DON. •Deposited DON should not be neglected when evaluating its ecological impacts. -- Synthesis of DON deposition across China implied regional importance of anthropogenic sources, and an observation in Northeast China suggested the ecological significances of the DON flux should be considered

Particle concentration and flux dynamics in the atmospheric boundary layer as the indicator of formation mechanism

DEFF Research Database (Denmark)

Lauros, J.; Sogachev, Andrey; Smolander, S.

2011-01-01

the atmospheric boundary layer during nucleation event days shows a highly dynamical picture, where particle formation is coupled with chemistry and turbulent transport. We have demonstrated the suitability of our turbulent mixing scheme in reproducing the most important characteristics of particle dynamics...... within the boundary layer. Deposition and particle flux simulations show that deposition affects noticeably only the smallest particles...

Atmospheric neutrino fluxes

International Nuclear Information System (INIS)

Perkins, D.H.

1984-01-01

The atmospheric neutrino fluxes, which are responsible for the main background in proton decay experiments, have been calculated by two independent methods. There are discrepancies between the two sets of results regarding latitude effects and up-down asymmetries, especially for neutrino energies Esub(ν) < 1 GeV. (author)

Characterization of the atmospheric muon flux in IceCube

Science.gov (United States)

Aartsen, M. G.; Abraham, K.; Ackermann, M.; Adams, J.; Aguilar, J. A.; Ahlers, M.; Ahrens, M.; Altmann, D.; Anderson, T.; Archinger, M.; Argüelles, C.; Arlen, T. C.; Auffenberg, J.; Bai, X.; Barwick, S. W.; Baum, V.; Bay, R.; Beatty, J. J.; Becker Tjus, J.; Becker, K.-H.; Beiser, E.; BenZvi, S.; Berghaus, P.; Berley, D.; Bernardini, E.; Bernhard, A.; Besson, D. Z.; Binder, G.; Bindig, D.; Bissok, M.; Blaufuss, E.; Blumenthal, J.; Boersma, D. J.; Bohm, C.; Börner, M.; Bos, F.; Bose, D.; Böser, S.; Botner, O.; Braun, J.; Brayeur, L.; Bretz, H.-P.; Brown, A. M.; Buzinsky, N.; Casey, J.; Casier, M.; Cheung, E.; Chirkin, D.; Christov, A.; Christy, B.; Clark, K.; Classen, L.; Coenders, S.; Cowen, D. F.; Cruz Silva, A. H.; Daughhetee, J.; Davis, J. C.; Day, M.; de André, J. P. A. M.; De Clercq, C.; Dembinski, H.; De Ridder, S.; Desiati, P.; de Vries, K. D.; de Wasseige, G.; de With, M.; DeYoung, T.; Díaz-Vélez, J. C.; Dumm, J. P.; Dunkman, M.; Eagan, R.; Eberhardt, B.; Ehrhardt, T.; Eichmann, B.; Euler, S.; Evenson, P. A.; Fadiran, O.; Fahey, S.; Fazely, A. R.; Fedynitch, A.; Feintzeig, J.; Felde, J.; Filimonov, K.; Finley, C.; Fischer-Wasels, T.; Flis, S.; Fuchs, T.; Glagla, M.; Gaisser, T. K.; Gaior, R.; Gallagher, J.; Gerhardt, L.; Ghorbani, K.; Gier, D.; Gladstone, L.; Glüsenkamp, T.; Goldschmidt, A.; Golup, G.; Gonzalez, J. G.; Góra, D.; Grant, D.; Gretskov, P.; Groh, J. C.; Groß, A.; Ha, C.; Haack, C.; Haj Ismail, A.; Hallgren, A.; Halzen, F.; Hansmann, B.; Hanson, K.; Hebecker, D.; Heereman, D.; Helbing, K.; Hellauer, R.; Hellwig, D.; Hickford, S.; Hignight, J.; Hill, G. C.; Hoffman, K. D.; Hoffmann, R.; Holzapfel, K.; Homeier, A.; Hoshina, K.; Huang, F.; Huber, M.; Huelsnitz, W.; Hulth, P. O.; Hultqvist, K.; In, S.; Ishihara, A.; Jacobi, E.; Japaridze, G. S.; Jero, K.; Jurkovic, M.; Kaminsky, B.; Kappes, A.; Karg, T.; Karle, A.; Kauer, M.; Keivani, A.; Kelley, J. L.; Kemp, J.; Kheirandish, A.; Kiryluk, J.; Kläs, J.; Klein, S. R.; Kohnen, G.; Koirala, R.; Kolanoski, H.; Konietz, R.; Koob, A.; Köpke, L.; Kopper, C.; Kopper, S.; Koskinen, D. J.; Kowalski, M.; Krings, K.; Kroll, G.; Kroll, M.; Kunnen, J.; Kurahashi, N.; Kuwabara, T.; Labare, M.; Lanfranchi, J. L.; Larson, M. J.; Lesiak-Bzdak, M.; Leuermann, M.; Leuner, J.; Lünemann, J.; Madsen, J.; Maggi, G.; Mahn, K. B. M.; Maruyama, R.; Mase, K.; Matis, H. S.; Maunu, R.; McNally, F.; Meagher, K.; Medici, M.; Meli, A.; Menne, T.; Merino, G.; Meures, T.; Miarecki, S.; Middell, E.; Middlemas, E.; Miller, J.; Mohrmann, L.; Montaruli, T.; Morse, R.; Nahnhauer, R.; Naumann, U.; Niederhausen, H.; Nowicki, S. C.; Nygren, D. R.; Obertacke, A.; Olivas, A.; Omairat, A.; O'Murchadha, A.; Palczewski, T.; Pandya, H.; Paul, L.; Pepper, J. A.; Pérez de los Heros, C.; Pfendner, C.; Pieloth, D.; Pinat, E.; Posselt, J.; Price, P. B.; Przybylski, G. T.; Pütz, J.; Quinnan, M.; Rädel, L.; Rameez, M.; Rawlins, K.; Redl, P.; Reimann, R.; Relich, M.; Resconi, E.; Rhode, W.; Richman, M.; Richter, S.; Riedel, B.; Robertson, S.; Rongen, M.; Rott, C.; Ruhe, T.; Ryckbosch, D.; Saba, S. M.; Sabbatini, L.; Sander, H.-G.; Sandrock, A.; Sandroos, J.; Sarkar, S.; Schatto, K.; Scheriau, F.; Schimp, M.; Schmidt, T.; Schmitz, M.; Schoenen, S.; Schöneberg, S.; Schönwald, A.; Schukraft, A.; Schulte, L.; Seckel, D.; Seunarine, S.; Shanidze, R.; Smith, M. W. E.; Soldin, D.; Spiczak, G. M.; Spiering, C.; Stahlberg, M.; Stamatikos, M.; Stanev, T.; Stanisha, N. A.; Stasik, A.; Stezelberger, T.; Stokstad, R. G.; Stößl, A.; Strahler, E. A.; Ström, R.; Strotjohann, N. L.; Sullivan, G. W.; Sutherland, M.; Taavola, H.; Taboada, I.; Ter-Antonyan, S.; Terliuk, A.; Tešić, G.; Tilav, S.; Toale, P. A.; Tobin, M. N.; Tosi, D.; Tselengidou, M.; Turcati, A.; Unger, E.; Usner, M.; Vallecorsa, S.; van Eijndhoven, N.; Vandenbroucke, J.; van Santen, J.; Vanheule, S.; Veenkamp, J.; Vehring, M.; Voge, M.; Vraeghe, M.; Walck, C.; Wallraff, M.; Wandkowsky, N.; Weaver, Ch.; Wendt, C.; Westerhoff, S.; Whelan, B. J.; Whitehorn, N.; Wichary, C.; Wiebe, K.; Wiebusch, C. H.; Wille, L.; Williams, D. R.; Wissing, H.; Wolf, M.; Wood, T. R.; Woschnagg, K.; Xu, D. L.; Xu, X. W.; Xu, Y.; Yáñez, J. P.; Yodh, G.; Yoshida, S.; Zarzhitsky, P.; Zoll, M.

2016-05-01

Muons produced in atmospheric cosmic ray showers account for the by far dominant part of the event yield in large-volume underground particle detectors. The IceCube detector, with an instrumented volume of about a cubic kilometer, has the potential to conduct unique investigations on atmospheric muons by exploiting the large collection area and the possibility to track particles over a long distance. Through detailed reconstruction of energy deposition along the tracks, the characteristics of muon bundles can be quantified, and individual particles of exceptionally high energy identified. The data can then be used to constrain the cosmic ray primary flux and the contribution to atmospheric lepton fluxes from prompt decays of short-lived hadrons. In this paper, techniques for the extraction of physical measurements from atmospheric muon events are described and first results are presented. The multiplicity spectrum of TeV muons in cosmic ray air showers for primaries in the energy range from the knee to the ankle is derived and found to be consistent with recent results from surface detectors. The single muon energy spectrum is determined up to PeV energies and shows a clear indication for the emergence of a distinct spectral component from prompt decays of short-lived hadrons. The magnitude of the prompt flux, which should include a substantial contribution from light vector meson di-muon decays, is consistent with current theoretical predictions. The variety of measurements and high event statistics can also be exploited for the evaluation of systematic effects. In the course of this study, internal inconsistencies in the zenith angle distribution of events were found which indicate the presence of an unexplained effect outside the currently applied range of detector systematics. The underlying cause could be related to the hadronic interaction models used to describe muon production in air showers.

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

Background concentrations and fluxes of atmospheric ammonia over a deciduous forest

DEFF Research Database (Denmark)

Hansen, K.; Pryor, S. C.; Boegh, E.

2015-01-01

. In this study, we present two months of half-hourly NH3 fluxes and concentrations measured using a Relaxed Eddy Accumulation system during late summer and fall 2013 above a remote forest site in the central Midwest in USA. Supplementary nitric acid (HNO3) flux and size-resolved aerosol-N measurements are used.......11 μg NH3-N m−2 s−1. The wetness of the forest surfaces (assessed using a proxy of time since precipitation) was found to be crucial in controlling both deposition and emission of atmospheric NH3. Size resolved aerosol concentrations (of NH4+, NO3−, Cl− and SO42−) indicated that the aerosol and gas...

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.

The concentration, source and deposition flux of ammonium and nitrate in atmospheric particles during dust events at a coastal site in northern China

Science.gov (United States)

Qi, Jianhua; Liu, Xiaohuan; Yao, Xiaohong; Zhang, Ruifeng; Chen, Xiaojing; Lin, Xuehui; Gao, Huiwang; Liu, Ruhai

2018-01-01

Asian dust has been reported to carry anthropogenic reactive nitrogen during transport from source areas to the oceans. In this study, we attempted to characterize NH4+ and NO3- in atmospheric particles collected at a coastal site in northern China during spring dust events from 2008 to 2011. Based on the mass concentrations of NH4+ and NO3- in each total suspended particle (TSP) sample, the samples can be classified into increasing or decreasing types. In Category 1, the concentrations of NH4+ and NO3- were 20-440 % higher in dust day samples relative to samples collected immediately before or after a dust event. These concentrations decreased by 10-75 % in the dust day samples in Categories 2 and 3. Back trajectory analysis suggested that multiple factors, such as the transport distance prior to the reception site, the mixing layer depth on the transport route and the residence time across highly polluted regions, might affect the concentrations of NH4+ and NO3-. NH4+ in the dust day samples was likely either in the form of ammonium salts existing separately to dust aerosols or as the residual of incomplete reactions between ammonium salts and carbonate salts. NO3- in the dust day samples was attributed to various formation processes during the long-range transport. The positive matrix factorization (PMF) receptor model results showed that the contribution of soil dust increased from 23 to 36 % on dust days, with decreasing contributions from local anthropogenic inputs and associated secondary aerosols. The estimated deposition flux of NNH4++NO3- varied greatly from event to event; e.g., the dry deposition flux of NNH4++NO3- increased by 9-285 % in Category 1 but decreased by 46-73 % in Category 2. In Category 3, the average dry deposition fluxes of particulate nitrate and ammonium decreased by 46 % and increased by 10 %, respectively, leading to 11-48 % decrease in the fluxes of NNH4++NO3-.

Seasonal variability in 7Be depositional fluxes at Granada, Spain

International Nuclear Information System (INIS)

Gonzalez-Gomez, C.; Azahra, M.; Lopez-Penalver, J.J.; Camacho-Garcia, A.; Bardouni, T.El.; Boukhal, H.

2006-01-01

Measurement of 7 Be depositional fluxes at Granada, Spain (37 o 10'50''N-3 o 35'44''W, altitude 670 m) in the period 1995 through 1998 indicates substantial variations between the four seasons and also between corresponding seasons in different years, ranging from 23.6 to 242 Bq m -2 per season. A strongly positive correlation with precipitation is shown, which explains about 70% of the variations in the 7 Be depositional fluxes over the 16 seasons studied. The depositional 7 Be flux is on the average highest in the fall and lowest in the summer. The study shows that precipitation primarily controls the 7 Be depositional flux and plays a dominant role in the removal of 7 Be from the troposphere. The average annual 7 Be depositional flux at Granada amounts to 469+145 Bq m -2

Fission products in National Atmospheric Deposition Program—Wet deposition samples prior to and following the Fukushima Dai-Ichi Nuclear Power Plant incident, March 8?April 5, 2011

Science.gov (United States)

Wetherbee, Gregory A.; Debey, Timothy M.; Nilles, Mark A.; Lehmann, Christopher M.B.; Gay, David A.

2012-01-01

Radioactive isotopes I-131, Cs-134, or Cs-137, products of uranium fission, were measured at approximately 20 percent of 167 sampled National Atmospheric Deposition Program monitoring sites in North America (primarily in the contiguous United States and Alaska) after the Fukushima Dai-Ichi Nuclear Power Plant incident on March 12, 2011. Samples from the National Atmospheric Deposition Program were analyzed for the period of March 8-April 5, 2011. Calculated 1- or 2-week radionuclide deposition fluxes at 35 sites from Alaska to Vermont ranged from 0.47 to 5,100 Becquerels per square meter during the sampling period of March 15-April 5, 2011. No fission-product isotopes were measured in National Atmospheric Deposition Program samples obtained during March 8-15, 2011, prior to the arrival of contaminated air in North America.

Calculation of atmospheric neutrino flux using the interaction model calibrated with atmospheric muon data

International Nuclear Information System (INIS)

Honda, M.; Kajita, T.; Kasahara, K.; Midorikawa, S.; Sanuki, T.

2007-01-01

Using the 'modified DPMJET-III' model explained in the previous paper [T. Sanuki et al., preceding Article, Phys. Rev. D 75, 043005 (2007).], we calculate the atmospheric neutrino flux. The calculation scheme is almost the same as HKKM04 [M. Honda, T. Kajita, K. Kasahara, and S. Midorikawa, Phys. Rev. D 70, 043008 (2004).], but the usage of the 'virtual detector' is improved to reduce the error due to it. Then we study the uncertainty of the calculated atmospheric neutrino flux summarizing the uncertainties of individual components of the simulation. The uncertainty of K-production in the interaction model is estimated using other interaction models: FLUKA'97 and FRITIOF 7.02, and modifying them so that they also reproduce the atmospheric muon flux data correctly. The uncertainties of the flux ratio and zenith angle dependence of the atmospheric neutrino flux are also studied

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.

Atmospheric deposition of mercury in central Poland: Sources and seasonal trends

Science.gov (United States)

Siudek, Patrycja; Kurzyca, Iwona; Siepak, Jerzy

2016-03-01

Atmospheric deposition of total mercury was studied at two sites in central Poland, between April 2013 and October 2014. Hg in rainwater (bulk deposition) was analyzed in relation to meteorological parameters and major ions (H+, NO3-, Cl-, SO42 -) in order to investigate seasonal variation, identify sources and determine factors affecting atmospheric Hg chemistry and deposition. Total mercury concentrations varied between 1.24 and 22.1 ng L- 1 at the urban sampling site (Poznań) and between 0.57 and 18.3 ng L- 1 in the woodland protected area (Jeziory), with quite similar mean values of 6.96 and 6.37 ng L- 1, respectively. Mercury in precipitation exhibited lower spatial variability within the study domain (urban/forest transect) than the concentrations determined during other similar observations, reflecting the predominant influence of the same local sources. In our study, a significant seasonal pattern of Hg deposition was observed at both sampling sites, with higher and more variable concentrations of Hg reported for the urban area. In particular, deposition values of Hg were higher in the samples attributed to relatively large precipitation amounts in the summer and in those collected during the winter season (the result of higher contributions from combustion sources, i.e. intensive combustion of fossil fuels in residential and commercial boilers, individual power/heat-generating plants). In addition, a significant relationship between Hg concentration and precipitation amount was found while considering different types of wintertime samples (i.e. rain, snow and mixed precipitation). The analysis of backward trajectories showed that air masses arriving from polluted regions of western Europe and southern Poland largely affected the amount of Hg in rainwater. A seasonal variation in Hg deposition fluxes was also observed, with the maximum value of Hg in spring and minimum in winter. Our results indicated that rainwater Hg and, consequently, the wet deposition

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.

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

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.

In Situ Denitrification and Biological Nitrogen Fixation Under Enhanced Atmospheric Reactive Nitrogen Deposition in UK Peatlands

Science.gov (United States)

Ullah, Sami; Saiz Val, Ernesto; Sgouridis, Fotis; Peichl, Matthias; Nilsson, Mats

2017-04-01

Dinitrogen (N2) and nitrous oxide (N2O) losses due to denitrification and biological N2 fixation (BNF) are the most uncertain components of the nitrogen (N) cycle in peatlands under enhanced atmospheric reactive nitrogen (Nr) deposition. This uncertainty hampers our ability to assess the contribution of denitrification to the removal of biologically fixed and/or atmospherically deposited Nr in peatlands. This uncertainty emanates from the difficulty in measuring in situ soil N2 and N2O production and consumption in peatlands. In situ denitrification and its contribution to total N2O flux was measured monthly between April 2013 and October 2014 in peatlands in two UK catchments. An adapted 15N-Gas Flux method1 with low level addition of 15N tracer (0.03 ± 0.005 kg 15N ha-1) was used to measure denitrification and its contribution to net N2O production (DN2O/TN2O). BNF was measured in situ through incubation of selected sphagnum species under 15N2 gas tracer. Denitrification2 varied temporally and averaged 8 kg N-N2 ha-1 y-1. The contribution of denitrification was about 48% to total N2O flux3 of 0.05 kg N ha-1 y-1. Soil moisture, temperature, ecosystem respiration, pH and mineral N content mainly regulated the flux of N2 and N2O. Preliminary results showed suppression of BNF, which was 1.8 to 7 times lower in peatland mosses exposed to ˜15 to 20 kg N ha-1 y-1 Nr deposition in the UK than in peatland mosses in northern Sweden with background Nr deposition. Overall, the contribution of denitrification to Nr removal in the selected peatlands was ˜50% of the annual Nr deposition rates, making these ecosystems vulnerable to chronic N saturation. These results point to a need for a more comprehensive annual BNF measurement to more accurately account for total Nr input into peatlands and its atmospheric loss due to denitrification. References Sgouridis F, Stott A & Ullah S, 2016. Application of the 15N-Gas Flux method for measuring in situ N2 and N2O fluxes due to

Wet deposition flux of trace elements to the Adirondack region

International Nuclear Information System (INIS)

Huang, X.; Keskin, S.S.; Gullu, G.; Olmez, I.

2001-01-01

Wet deposition samples from two locations in the Adirondack region of New York were analyzed for trace elemental composition by instrumental neutron activation analysis. Annual fluxes of the measured species were determined by precipitation-weighted and linear-regression methods. Despite several episodes of high deposition fluxes, the cumulative areal wet deposition of trace elements increased fairly linearly (r 2 > 0.9) over the two year sampling period at both sites. This implies that short duration sampling programs may be used to estimate long-term fluxes and cumulative wet deposition impacts. Based on the magnitude of their fluxes, the measured species have been divided into four groups: acidic anions, electroneutral balancing cations, and minor and trace elements of anthropogenic origin. (author)

On extreme atmospheric and marine nitrogen fluxes and chlorophyll-a levels in the Kattegat Strait

Directory of Open Access Journals (Sweden)

C. B. Hasager

2003-01-01

Full Text Available A retrospective analysis is carried out to investigate the importance of the vertical fluxes of nitrogen to the marine sea surface layer in which high chlorophyll a levels may cause blooms of harmful algae and subsequent turn over and oxygen depletion at the bottom of the sea. Typically nitrogen is the limiting factor for phytoplankton in the Kattegat Strait during summer periods (May to August and the major nitrogen inputs come from the atmosphere and deep-water entrainment. The extreme reoccurrence values of nitrogen from atmospheric wet and dry deposition and deep-water flux entrainments are calculated by the periodic maximum method and the results are successfully compared to a map of chlorophyll return periods based on in-situ observations. The one-year return of extreme atmospheric wet deposition is around 60 mg N m-2 day-1 and 30 mg N m-2 day-1 for deep-water entrainment. Atmospheric nitrogen dry deposition is insignificant in the context of algal blooms. At longer time-scales e.g. at 10-year return, the nitrogen deep-water entrainment is larger than the extreme of atmospheric wet deposition. This indicates that the pool of nitrogen released from the sea bottom by deep-water entrainment forced by high winds greatly exceeds the atmospheric pool of nitrogen washed out by precipitation. At the frontal zone of the Kattegat Strait and Skagerrak, the nitrogen deep-water entrainment is very high and this explains the high 10-year return chlorophyll level at 8 mg m-3 in the Kattegat Strait. In the southern part, the extreme chlorophyll level is only 4 mg m-3 according to the statistics of a multi-year time-series of water samples. The chlorophyll level varies greatly in time and space as documented by a series of SeaWiFS satellite maps (OC4v4 algorithm of chlorophyll ScanFish and buoy observations from an experimental period in the Kattegat Strait. It is recommended to sample in-situ chlorophyll observation collocated in time to the satellite

Mercury fluxes over an Australian alpine grassland and observation of nocturnal atmospheric mercury depletion events

Directory of Open Access Journals (Sweden)

D. Howard

2018-01-01

Full Text Available Aerodynamic gradient measurements of the air–surface exchange of gaseous elemental mercury (GEM were undertaken over a 40 ha alpine grassland in Australia's Snowy Mountains region across a 3-week period during the late austral summer. Bi-directional GEM fluxes were observed throughout the study, with overall mean value of 0.2 ± 14.5 ng m−2 h−1 and mean nocturnal fluxes of −1.5 ± 7.8 ng m−2 h−1 compared to diurnal fluxes of 1.8 ± 18.6 ng m−2 h−1. Deposition velocities ranged from −2.2 to 2.9 cm s−1, whilst ambient GEM concentrations throughout the study were 0.59 ± 0.10 ng m−3. Cumulative GEM fluxes correlated well with 24 h running mean soil temperatures, and one precipitation event was shown to have a positive impact on diurnal emission fluxes. The underlying vegetation had largely senesced and showed little stomatal control on fluxes. Nocturnal atmospheric mercury depletion events (NAMDEs were observed concomitant with O3 depletion and dew formation under shallow, stable nocturnal boundary layers. A mass balance box model was able to reproduce ambient GEM concentration patterns during NAMDE and non-NAMDE nights without invoking chemical oxidation of GEM throughout the column, indicating a significant role of surface processes controlling deposition in these events. Surface deposition was enhanced under NAMDE nights, though uptake to dew likely represents less than one-fifth of this enhanced deposition. Instead, enhancement of the surface GEM gradient as a result of oxidation at the surface in the presence of dew is hypothesised to be responsible for a large portion of GEM depletion during these particular events. GEM emission pulses following nights with significant deposition provide evidence for the prompt recycling of 17 % of deposited mercury, with the remaining portion retained in surface sinks. The long-term impacts of any sinks are however likely to be minimal, as

Trends of deposition fluxes and loadings of sulfur dioxide and nitrogen oxides in the artificial Three Northern Regions Shelter Forest across northern China

International Nuclear Information System (INIS)

Zhang, Xiaodong; Huang, Tao; Zhang, Leiming; Gao, Hong; Shen, Yanjie; Ma, Jianmin

2015-01-01

This study provides the first estimate of dry deposition fluxes of criteria air pollutants (SO_2 and NO_x) across the Three Northern Regions Shelter Forest (TNRSF) region in Northern China and their long-term trends from 1982 to 2010 using the inferential method. Dry deposition velocities of SO_2 and NO_x increased in many places of the TNRSF up to 118.2% for SO_2 and 112.1% for NO_x over the last three decades due to the increased vegetation coverage over the TNRSF. The highest atmospheric deposition fluxes of SO_2 and NO_x were found in the Central-North China region, followed by the Northeast and the Northwest China regions of the TNRSF. A total of 820,000 t SO_2 and 218,000 t NO_x was estimated to be removed from the atmosphere through dry deposition process over the TNRSF from 1982 to 2010. About 50% of the total removal occurred in the Central-North China region. The estimated total SO_2 and NO_x dry deposition fluxes from 1982 to 2010 between a TNRSF site in this region and an adjacent farmland outside the TNRSF showed that the fluxes of these two chemicals at the TNRSF site were the factors of 2–3 greater than their fluxes in the farmland. - Highlights: • We investigate removal of air pollutants by the Three-North Shelter Forest (Green Great Wall) in China. • The trend of SO_2 and NO_x dry deposition velocity and flux over the TNRSF increase over the last three decades. • Increasing trends of deposition fluxes of SO_2 and NO_x are more evident in Central-North and Northeast China. • We show higher deposition fluxes of SO_2 and NO_x within the TNSF than outside TNRSF. • Stronger removal of air pollutants by the TNRSF is expected when other criteria air pollutants are taken into account. - The TNRSF is demonstrated to be an effective sink for SO_2 and NO_x and has increased the removal of air pollutants from Northern China.

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

Determination of depositional beryllium-10 fluxes in the area of the Laptev sea

Energy Technology Data Exchange (ETDEWEB)

Strobl, C.; Schulz, V.; Schaeper, S.; Molnar, M.; Baumann, S.; Mangini [Heidelberger Akademie der Wissenschaften, Heidelberg (Germany); Kubik, P.W. [Paul Scherrer Inst. (PSI), Villigen (Switzerland)

1997-09-01

A huge amount of continental {sup 10}Be is delivered to the Arctic Ocean through the rivers. Our investigations show that the most extensive part of it is deposited directly in the shelf areas. The determined sedimentation flux densities in the continental slope and in the Central Arctic Ocean are in the range of the assumed atmospheric input of {sup 10}Be and therefore clearly lower than in the shelf areas. (author) 1 fig., 2 refs.

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.

Atmospheric deposition of methanol over the Atlantic Ocean

Science.gov (United States)

Yang, Mingxi; Nightingale, Philip D.; Beale, Rachael; Liss, Peter S.; Blomquist, Byron; Fairall, Christopher

2013-01-01

In the troposphere, methanol (CH3OH) is present ubiquitously and second in abundance among organic gases after methane. In the surface ocean, methanol represents a supply of energy and carbon for marine microbes. Here we report direct measurements of air–sea methanol transfer along a ∼10,000-km north–south transect of the Atlantic. The flux of methanol was consistently from the atmosphere to the ocean. Constrained by the aerodynamic limit and measured rate of air–sea sensible heat exchange, methanol transfer resembles a one-way depositional process, which suggests dissolved methanol concentrations near the water surface that are lower than what were measured at ∼5 m depth, for reasons currently unknown. We estimate the global oceanic uptake of methanol and examine the lifetimes of this compound in the lower atmosphere and upper ocean with respect to gas exchange. We also constrain the molecular diffusional resistance above the ocean surface—an important term for improving air–sea gas exchange models. PMID:24277830

Wet deposition of mercury in Qingdao, a coastal urban city in China: Concentrations, fluxes, and influencing factors

Science.gov (United States)

Chen, Lufeng; Li, Yanbin; Liu, Chang; Guo, Lina; Wang, Xiulin

2018-02-01

Mercury (Hg) is a global pollutant of public concern because of its high toxicity and capability for worldwide distribution via long-range atmospheric transportation. Wet atmospheric deposition is an important source of Hg in both terrestrial and aquatic environments. Concentrations of various Hg species in precipitation were monitored from March 2016 to February 2017 in a coastal urban area of Qingdao, and their wet deposition fluxes were estimated. The results showed that the volume-weighted mean (VWM) concentrations of total mercury (THg), reactive mercury (RHg), dissolved THg (DTHg), particulate THg (PTHg), total methylmercury (TMeHg), and dissolved and particulate MeHg (DMeHg and PMeHg) in Qingdao's precipitation were 13.6, 1.5, 5.4, 8.2, 0.38, 0.15, and 0.22 ng L-1, respectively, and their annual deposition fluxes were estimated to be 5703.0 (THg), 666.6 (RHg), 2304.0 (DTHg), 3470.4 (PTHg), 161.6 (TMeHg), 64.0 (DMeHg), and 95.7 (PMeHg) ng m-2 y-1, respectively. A relatively high proportion of MeHg in THg was observed in precipitation (3.0 ± 2.6%) possibly due to higher methylation and contributions from an oceanic source to MeHg in the precipitation. Obvious seasonal variations in Hg concentrations and deposition fluxes were observed in the precipitation in Qingdao. Correlation analyses and multiple regression analyses showed that SO2, pH, and NO3- were the controlling factors for THg in precipitation, whereas the MeHg concentration was primarily controlled by the SO2, WS, Cl-, and THg concentrations. PM2.5 and Cl- were the major controlling factors for PMeHg/TMeHg, whereas the TMeHg/THg ratio was mainly influenced by Cl-. The THg and MeHg fluxes were primarily controlled by precipitation, whereas Cl- was also an important factor for the MeHg wet deposition flux. The results of a 72-h backward trajectory analysis in the study region with the Hybrid Single Particle Lagrangian Integrated Trajectory (HYSPLIT) model indicated that Hg deposition in Qingdao mainly

Effects of atmospheric deposition nitrogen flux and its composition on soil solution chemistry from a red soil farmland, southeast China.

Science.gov (United States)

Cui, Jian; Zhou, Jing; Peng, Ying; Chan, Andrew; Mao, Jingdong

2015-12-01

A detailed study on the solution chemistry of red soil in South China is presented. Data are collected from two simulated column-leaching experiments with an improved setup to evaluate the effects of atmospheric N deposition (ADN) composition and ADN flux on agricultural soil acidification using a (15)N tracer technique and an in situ soil solution sampler. The results show that solution pH values decline regardless of the increase of the NH4(+)/NO3(-) ratio in the ADN composition or ADN flux, while exchangeable Al(3+), Ca(2+), Mg(2+), and K(+) concentrations increase at different soil depths (20, 40, and 60 cm). Compared with the control, ADN (60 kg per ha per year N, NH4(+)/NO3(-) ratio of 2 : 1) decreases solution pH values, increases solution concentrations of NO3(-)-N, Al(3+), Ca(2+) and Mg(2+) at the middle and lower soil depths, and promotes their removal. NH4(+)-N was not detected in red soil solutions of all the three soil layers, which might be attributed to effects of nitrification, absorption and fixation in farmland red soil. Some of the NO3(-)-N concentrations at 40-60 cm soil depth exceed the safe drinking level of 10 mg L(-1), especially when the ADN flux is beyond 60 kg ha(-1) N. These features are critical for understanding the ADN agro-ecological effects, and for future assessment of ecological critical loads of ADN in red soil farmlands.

Extraction of the atmospheric neutrino fluxes from experimental event rate data

NARCIS (Netherlands)

Gonzalez-Garcia, M. C.; Maltoni, M.; Rojo, J.

2007-01-01

The precise knowledge of the atmospheric neutrino fluxes is a key ingredient in the interpretation of the results from any atmospheric neutrino experiment. In the standard atmospheric neutrino data analysis, these fluxes are theoretical inputs obtained from sophisticated numerical calculations. In

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

Spatial pattern of nitrogen deposition flux over Czech forests: a novel approach accounting for unmeasured nitrogen species

Science.gov (United States)

Hůnová, Iva; Stoklasová, Petra; Kurfürst, Pavel; Vlček, Ondřej; Schovánková, Jana; Stráník, Vojtěch

2015-04-01

atmospheric nitrogen deposition flux over the Czech forests collating all available data and model results. The aim of the presented study is to provide an improved, more reliable and more realistic estimate of spatial pattern of nitrogen deposition flux over one country. This has so far been based standardly on measurements of ambient N/NOx concentrations as dry deposition proxy, and N/NH4+ and N/NO3- as wet deposition proxy. For estimate of unmeasured species contributing to dry deposition, we used an Eulerian photochemical dispersion model CAMx, the Comprehensive Air Quality Model with extensions (ESSS, 2011), coupled with a high resolution regional numeric weather prediction model Aladin (Vlček, Corbet, 2011). Contribution of fog was estimated using a geostatistical data driven model. Final maps accounting for unmeasured species clearly indicate, that so far used approach results in substantial underestimation of nitrogen deposition flux. Substitution of unmeasured nitrogen species by modeled values seems to be a plausible way for approximation of total nitrogen deposition, and getting more realistic spatial pattern as input for further studies of likely nitrogen impacts on ecosystems. Acknowledgements: We would like to acknowledge the grants GA14-12262S - Effects of changing growth conditions on tree increment, stand production and vitality - danger or opportunity for the Central-European forestry?, and NAZV QI112A168 (ForSoil) of the Czech Ministry for Agriculture for support of this contribution. The input data used for the analysis were provided by the Czech Hydrometeorological Institute. References: Bobbink, R., Hicks, K., Galloway, J., Spranger, T., Alkemade, R. et al. (2010): Global Assessment of Nitrogen Deposition Effects on Terrestrial Plant Diversity: a Synthesis. Ecological Applications 20 (1), 30-59. Fowler D., O'Donoghue M., Muller J.B.A, et al. (2005): A chronology of nitrogen deposition in the UK between 1900 and 2000. Watter, Air & Soil Pollution: Focus

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

Atmospheric deposition of trace elements recorded in snow from the Mt. Nyainqêntanglha region, southern Tibetan Plateau.

Science.gov (United States)

Huang, Jie; Kang, Shichang; Zhang, Qianggong; Guo, Junming; Chen, Pengfei; Zhang, Guoshuai; Tripathee, Lekhendra

2013-08-01

In May 2009, snowpit samples were collected from a high-elevation glacier in the Mt. Nyainqêntanglha region on the southern Tibetan Plateau. A set of elements (Al, V, Cr, Mn, Co, Ni, Cu, Zn, Cd, Hg and Pb) was analyzed to investigate the concentrations, deposition fluxes of trace elements, and the relative contributions from anthropogenic and natural sources deposited on the southern Tibetan Plateau. Concentrations of most of the trace elements in snowpit samples from the Zhadang glacier are significantly lower than those examined from central Asia (e.g., eastern Tien Shan), with higher concentrations during the non-monsoon season than during the monsoon season. The elements of Al, V, Cr, Mn, Co, and Ni display low crustal enrichment factors (EFs), while Cu, Zn, Cd, Hg, and Pb show high EF values in the snow samples, suggesting anthropogenic inputs are potentially important for these elements in the remote, high-elevation atmosphere on the southern Tibetan Plateau. Together with the fact that the concentration levels of such elements in the Mt. Nyainqêntanglha region are significantly higher than those observed on the south edge of the Tibetan Plateau, our results suggest that the high-elevation atmosphere on the southern Tibetan Plateau may be more sensitive to variations in the anthropogenic emissions of atmospheric trace elements than that in the central Himalayas. Moreover, the major difference between deposition fluxes estimated in our snow samples and those recently measured at Nam Co Station for elements such as Cr and Cu may suggest that atmospheric deposition of some of trace elements reconstructed from snowpits and ice cores could be grossly underestimated on the Tibetan Plateau. Copyright © 2013 Elsevier Ltd. All rights reserved.

Heavy metals in atmospheric surrogate dry deposition

Science.gov (United States)

Morselli; Cecchini; Grandi; Iannuccilli; Barilli; Olivieri

1999-02-01

This paper describes a methodological approach for the assessment of the amount of surrogate dry deposition of several toxic heavy metals (Cd, Cr, Cu, Ni, Pb, V, Zn) associated with atmospheric particulate matter at ground level. The objectives of the study were twofold: i) the evaluation of several techniques for the digestion of dry deposition samples for trace metal analysis; ii) the comparison of the results from two samplers with different collecting surfaces. A dry solid surface sampler (DRY sampler, Andersen--USA) and a water layer surface sampler (DAS sampler--MTX Italy) were employed. The samples were collected over a one-year period in an urban site of Bologna (northern Italy). A description is given of the complete procedure, from sampling to data elaboration, including sample storage, digestion and analytical methods. According to the results obtained with three different digestion techniques (Teflon bomb, microwave digester and Teflon flask with vapour cooling system), the highest recovery rate was achieved by the Teflon bomb procedure employing an NBS 1648 Standard Reference Material; 90-95% of the elements considered were recovered by dissolution in a pressurized Teflon bomb with an HNO3-HF mixture. Given these results, the technique was adopted for dry deposition sample digestion. On the basis of the amount of heavy metals measured as monthly deposition fluxes (microg/m2), the collecting efficiency of the DAS sampler for a number of elements was found to be as much as two to three times greater than that of the DRY sampler.

Chromium speciation in rainwater: temporal variability and atmospheric deposition

Energy Technology Data Exchange (ETDEWEB)

Kieber, R.J.; Willey, J.D.; Zvalaren, S.D. [University of North Carolina at Wilmington, Wilmington, NC (United States). Dept. of Chemistry

2002-12-15

Chromium is released into the atmosphere by a variety of anthropogenic activities which include steel manufacturing, leather tanning, wood presentation and fossil fuel combustion. The concentrations of the various chromium species were determined in 89 rainwater samples collected in Wilmington, NC from October 1, 1999 to December 31, 2001. Volume weighted annual average concentrations of Cr{sub total}, particulate Cr, Cr(III)(aq), and Cr(VI)(aq) were 4.6, 2.2, 0.8 and 1.2 nM, respectively. There was distinct seasonal and diurnal variability in the concentrations of the various chromium species. Chromium emissions to the global atmosphere by both natural and anthropogenic sources are estimated to be 2.2 x 10{sup 9} mol/yr. Using rainwater concentration data along with other published rainwater Cr concentrations and an estimate for total global annual rain, the total global flux of chromium removed from the atmosphere via wet deposition is 2.1 x 10{sup 9} mol/yr. This represents complete removal of Cr and indicates that essentially all chromium released into the global atmosphere is removed via rain. About half this chromium is dissolved with roughly equal concentrations of toxic Cr(VI) and relatively harmless Cr(III) species. 48 refs., 4 figs., 3 tabs.

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

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.

Modeling the biogeochemical impact of atmospheric phosphate deposition from desert dust and combustion sources to the Mediterranean Sea

Science.gov (United States)

Richon, Camille; Dutay, Jean-Claude; Dulac, François; Wang, Rong; Balkanski, Yves

2018-04-01

Daily modeled fields of phosphate deposition to the Mediterranean from natural dust, anthropogenic combustion and wildfires were used to assess the effect of this external nutrient on marine biogeochemistry. The ocean model used is a high-resolution (1/12°) regional coupled dynamical-biogeochemical model of the Mediterranean Sea (NEMO-MED12/PISCES). The input fields of phosphorus are for 2005, which are the only available daily resolved deposition fields from the global atmospheric chemical transport model LMDz-INCA. Traditionally, dust has been suggested to be the main atmospheric source of phosphorus, but the LMDz-INCA model suggests that combustion is dominant over natural dust as an atmospheric source of phosphate (PO4, the bioavailable form of phosphorus in seawater) for the Mediterranean Sea. According to the atmospheric transport model, phosphate deposition from combustion (Pcomb) brings on average 40.5×10-6 mol PO4 m-2 yr-1 over the entire Mediterranean Sea for the year 2005 and is the primary source over the northern part (e.g., 101×10-6 mol PO4 m-2 yr-1 from combustion deposited in 2005 over the north Adriatic against 12.4×10-6 from dust). Lithogenic dust brings 17.2×10-6 mol PO4 m-2 yr-1 on average over the Mediterranean Sea in 2005 and is the primary source of atmospheric phosphate to the southern Mediterranean Basin in our simulations (e.g., 31.8×10-6 mol PO4 m-2 yr-1 from dust deposited in 2005 on average over the south Ionian basin against 12.4×10-6 from combustion). The evaluation of monthly averaged deposition flux variability of Pdust and Pcomb for the 1997-2012 period indicates that these conclusions may hold true for different years. We examine separately the two atmospheric phosphate sources and their respective flux variability and evaluate their impacts on marine surface biogeochemistry (phosphate concentration, chlorophyll a, primary production). The impacts of the different phosphate deposition sources on the biogeochemistry of the

Powder Flux Regulation in the Laser Material Deposition Process

Science.gov (United States)

Arrizubieta, Jon Iñaki; Wegener, Maximiliam; Arntz, Kristian; Lamikiz, Aitzol; Ruiz, Jose Exequiel

In the present research work a powder flux regulation system has been designed, developed and validated with the aim of improving the Laser Material Deposition (LMD) process. In this process, the amount of deposited material per substrate surface unit area depends on the real feed rate of the nozzle. Therefore, a regulation system based on a solenoid valve has been installed at the nozzle entrance in order to control the powder flux. The powder flux control has been performed based on the machine real feed rate, which is compared with the programmed feed rate. An instantaneous velocity error is calculated and the powder flow is controlled as a function of this variation using Pulse Width Modulation (PWM) signals. Thereby, in zones where the Laser Material Deposition machine reduces the feed rate due to a trajectory change, powder accumulation can be avoided and the generated clads would present a homogeneous shape.

Atmospheric pressure plasma enhanced chemical vapor deposition of zinc oxide and aluminum zinc oxide

International Nuclear Information System (INIS)

Johnson, Kyle W.; Guruvenket, Srinivasan; Sailer, Robert A.; Ahrenkiel, S. Phillip; Schulz, Douglas L.

2013-01-01

Zinc oxide (ZnO) and aluminum-doped zinc oxide (AZO) thin films were deposited via atmospheric pressure plasma enhanced chemical vapor deposition. A second-generation precursor, bis(1,1,1,5,5,5-hexafluoro-2,4-pentanedionato)(N,N′-diethylethylenediamine) zinc, exhibited significant vapor pressure and good stability at one atmosphere where a vaporization temperature of 110 °C gave flux ∼ 7 μmol/min. Auger electron spectroscopy confirmed that addition of H 2 O to the carrier gas stream mitigated F contamination giving nearly 1:1 metal:oxide stoichiometries for both ZnO and AZO with little precursor-derived C contamination. ZnO and AZO thin film resistivities ranged from 14 to 28 Ω·cm for the former and 1.1 to 2.7 Ω·cm for the latter. - Highlights: • A second generation precursor was utilized for atmospheric pressure film growth. • Addition of water vapor to the carrier gas stream led to a marked reduction of ZnF 2 . • Carbonaceous contamination from the precursor was minimal

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

Uncertainties in (E)UV model atmosphere fluxes

Science.gov (United States)

Rauch, T.

2008-04-01

Context: During the comparison of synthetic spectra calculated with two NLTE model atmosphere codes, namely TMAP and TLUSTY, we encounter systematic differences in the EUV fluxes due to the treatment of level dissolution by pressure ionization. Aims: In the case of Sirius B, we demonstrate an uncertainty in modeling the EUV flux reliably in order to challenge theoreticians to improve the theory of level dissolution. Methods: We calculated synthetic spectra for hot, compact stars using state-of-the-art NLTE model-atmosphere techniques. Results: Systematic differences may occur due to a code-specific cutoff frequency of the H I Lyman bound-free opacity. This is the case for TMAP and TLUSTY. Both codes predict the same flux level at wavelengths lower than about 1500 Å for stars with effective temperatures (T_eff) below about 30 000 K only, if the same cutoff frequency is chosen. Conclusions: The theory of level dissolution in high-density plasmas, which is available for hydrogen only should be generalized to all species. Especially, the cutoff frequencies for the bound-free opacities should be defined in order to make predictions of UV fluxes more reliable.

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

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

Does historical wildfire activity alter metal fluxes to northern lakes?

Science.gov (United States)

Pelletier, N.; Chetelat, J.; Vermaire, J. C.; Palmer, M.; Black, J.; Pellisey, J.; Tracz, B.; van der Wielen, S.

2017-12-01

Current drought conditions in northwestern Canada are conducive to more frequent and severe wildfires that may mobilize mercury and other metals accumulated in soil and biomass. There is evidence that wildfires can remobilize and transport mercury within and outside catchments by atmospheric volatilization, particulate emissions and catchment soil erosion. However, the effect of fires on mercury fluxes to nearby lake sediments remains unclear. In this study, we use a combination of 10 dated lake sediment cores and four nearby ombrotrophic peatland cores to investigate the effects of wildfires on mercury fluxes to lake sediments. Lakes varying in catchment size and distance from recent fire events were sampled. Mercury concentrations in the environmental archives were measured, and macroscopic charcoal particles (>100 um) were counted at high resolution in the sediments to observe the co-variation of the local fire history and mercury fluxes. Mercury flux recorded in ombrotrophic peat cores provided an estimate of the historical atmospheric mercury flux from local and regional atmospheric deposition. The mercury flux recorded in lake sediments corresponds to the sum of direct atmospheric deposition and catchment transport. In combination, these archives will allow for the partitioning of mercury loading attributable to catchment transport from direct atmospheric deposition. After correcting the fluxes for particle focusing and terragenic elements input, flux from different lakes will be compared based on their catchment size and their temporal and spatial proximity known fire events. Altogether, our preliminary results using these paleolimnological methods will provide new insights on mercury transport processes that are predicted to become more important under a changing climate.

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

Crustal tracers in the atmosphere and ocean: Relating their concentrations, fluxes, and ages

Science.gov (United States)

Han, Qin

Crustal tracers are important sources of key limiting nutrients (e.g., iron) in remote ocean regions where they have a large impact on global biogeochemical cycles. However, the atmospheric delivery of bio-available iron to oceans via mineral dust aerosol deposition is poorly constrained. This dissertation aims to improve understanding and model representation of oceanic dust deposition and to provide soluble iron flux maps by testing observations of crustal tracer concentrations and solubilities against predictions from two conceptual solubility models. First, we assemble a database of ocean surface dissolved Al and incorporate Al cycling into the global Biogeochemical Elemental Cycling (BEC) model. The observed Al concentrations show clear basin-scale differences that are useful for constraining dust deposition. The dynamic mixed layer depth and Al residence time in the BEC model significantly improve the simulated dissolved Al field. Some of the remaining model-data discrepancies appear related to the neglect of aerosol size, age, and air mass characteristics in estimating tracer solubility. Next, we develop the Mass-Age Tracking method (MAT) to efficiently and accurately estimate the mass-weighted age of tracers. We apply MAT to four sizes of desert dust aerosol and simulate, for the first time, global distributions of aerosol age in the atmosphere and at deposition. These dust size and age distributions at deposition, together with independent information on air mass acidity, allow us to test two simple yet plausible models for predicting the dissolution of mineral dust iron and aluminum during atmospheric transport. These models represent aerosol solubility as controlled (1) by a diffusive process leaching nutrients from the dust into equilibrium with the liquid water coating or (2) by a process that continually dissolves nutrients in proportion to the particle surface area. The surface-controlled model better captures the spatial pattern of observed

Sensitivity of upper atmospheric emissions calculations to solar/stellar UV flux

Directory of Open Access Journals (Sweden)

Barthelemy Mathieu

2014-01-01

Full Text Available The solar UV (UltraViolet flux, especially the EUV (Extreme UltraViolet and FUV (Far UltraViolet components, is one of the main energetic inputs for planetary upper atmospheres. It drives various processes such as ionization, or dissociation which give rise to upper atmospheric emissions, especially in the UV and visible. These emissions are one of the main ways to investigate the upper atmospheres of planets. However, the uncertainties in the flux measurement or modeling can lead to biased estimates of fundamental atmospheric parameters, such as concentrations or temperatures in the atmospheres. We explore the various problems that can be identified regarding the uncertainties in solar/stellar UV flux by considering three examples. The worst case appears when the solar reflection component is dominant in the recorded spectrum as is seen for outer solar system measurements from HST (Hubble Space Telescope. We also show that the estimation of some particular line parameters (intensity and shape, especially Lyman α, is crucial, and that both total intensity and line profile are useful. In the case of exoplanets, the problem is quite critical since the UV flux of their parent stars is often very poorly known.

Atmospheric gamma-ray observation with the BETS detectorfor calibrating atmospheric neutrino flux calculations

CERN Document Server

Kasahara, K.; Torii, S.; Tamura, T.; Tateyama, N.; Yoshida, K.; Yamagami, T.; Saito, Y.; Nishimura, J.; Murakami, H.; Kobayashi, T.; Komori, Y.; Honda, M.; Ohuchi, T.; Midorikawa, S.; Yuda, T.

2002-01-01

We observed atmospheric gamma-rays around 10 GeV at balloon altitudes (15~25 km) and at a mountain (2770 m a.s.l). The observed results were compared with Monte Carlo calculations to find that an interaction model (Lund Fritiof1.6) used in an old neutrino flux calculation was not good enough for describing the observed values. In stead, we found that two other nuclear interaction models, Lund Fritiof7.02 and dpmjet3.03, gave much better agreement with the observations. Our data will serve for examining nuclear interaction models and for deriving a reliable absolute atmospheric neutrino flux in the GeV region.

Source contribution to the bulk atmospheric deposition of minor and trace elements in a Northern Spanish coastal urban area

Science.gov (United States)

Fernández-Olmo, Ignacio; Puente, Mariano; Montecalvo, Lucia; Irabien, Angel

2014-08-01

The bulk atmospheric deposition of the minor and trace elements As, Cd, Cr, Cu, Mn, Mo, Ni, Pb, Ti, V and Zn was investigated in Santander, a Northern Spanish coastal city. Bulk deposition samples were collected monthly for three years using a bottle/funnel device. Taking into account that heavy metals are bioavailable only in their soluble forms, water-soluble and water-insoluble fractions were evaluated separately for element concentration. The fluxes of the studied elements in the bulk deposition exhibited the following order: Zn > Mn ≫ Cu > Cr > Pb > V > Ni ≫ As > Mo > Cd. The fluxes of Zn and Mn were more than 10 times higher than those of the other elements, with maximum values of 554.5 and 334.1 μg m- 2 day- 1, respectively. Low solubilities (below 22%) were found for Cr, Ti and Pb, whereas the highest solubility was found for Zn (78%). With the exception of Cu, all of the studied metals in the water-soluble fraction of the atmospheric deposition showed seasonal dependence, due to the seasonal variability of precipitation. The enrichment factors (EFs) of Cu, Cd and Zn were higher than 100, indicating a clear anthropogenic origin. The EF of Mn (50) was below 100, but an exclusively industrial origin is suggested. Positive Matrix Factorisation (PMF) was used for the source apportionment of the studied minor and trace elements in the soluble fraction. Four factors were identified from PMF, and their chemical profiles were compared with those calculated from known sources that were previously identified in Santander Bay: two industrial sources, the first of which was characterised by Zn and Mn, which contributes 62.5% of the total deposition flux of the studied elements; a traffic source; and a maritime source. Zinc and Mn are considered to be the most characteristic pollutants of the studied area.

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

Science.gov (United States)

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.

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

Simulated Nitrogen Deposition has Minor Effects on Ecosystem Pools and Fluxes of Energy, Elements, and Biochemicals in a Northern Hardwoods Forest

Science.gov (United States)

Talhelm, A. F.; Pregitzer, K. S.; Burton, A. J.; Xia, M.; Zak, D. R.

2017-12-01

The elemental and biochemical composition of plant tissues is an important influence on primary productivity, decomposition, and other aspects of biogeochemistry. Human activity has greatly altered biogeochemical cycles in ecosystems downwind of industrialized regions through atmospheric nitrogen deposition, but most research on these effects focuses on individual elements or steps in biogeochemical cycles. Here, we quantified pools and fluxes of biomass, the four major organic elements (carbon, oxygen, hydrogen, nitrogen), four biochemical fractions (lignin, structural carbohydrates, cell walls, and soluble material), and energy in a mature northern hardwoods forest in Michigan. We sampled the organic and mineral soil, fine and coarse roots, leaf litter, green leaves, and wood for chemical analyses. We then combined these data with previously published and archival information on pools and fluxes within this forest, which included replicated plots receiving either ambient deposition or simulated nitrogen deposition (3 g N m-2 yr-1 for 18 years). Live wood was the largest pool of energy and all elements and biochemical fractions. However, the production of wood, leaf litter, and fine roots represented similar fluxes of carbon, hydrogen, oxygen, cell wall material, and energy, while nitrogen fluxes were dominated by leaf litter and fine roots. Notably, the flux of lignin via fine roots was 70% higher than any other flux. Experimental nitrogen deposition had relatively few significant effects, increasing foliar nitrogen, increasing the concentration of lignin in the soil organic horizon and decreasing pools of all elements and biochemical fractions in the soil organic horizon except nitrogen, lignin, and structural carbohydrates. Overall, we found that differences in tissue chemistry concentrations were important determinants of ecosystem-level pools and fluxes, but that nitrogen deposition had little effect on concentrations, pools, or fluxes in this mature forest

A climatological model for risk computations incorporating site- specific dry deposition influences

International Nuclear Information System (INIS)

Droppo, J.G. Jr.

1991-07-01

A gradient-flux dry deposition module was developed for use in a climatological atmospheric transport model, the Multimedia Environmental Pollutant Assessment System (MEPAS). The atmospheric pathway model computes long-term average contaminant air concentration and surface deposition patterns surrounding a potential release site incorporating location-specific dry deposition influences. Gradient-flux formulations are used to incorporate site and regional data in the dry deposition module for this atmospheric sector-average climatological model. Application of these formulations provide an effective means of accounting for local surface roughness in deposition computations. Linkage to a risk computation module resulted in a need for separate regional and specific surface deposition computations. 13 refs., 4 figs., 2 tabs

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 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

Determination of soluble ultra-trace metals and metalloids in rainwater and atmospheric deposition fluxes: a 2-year survey and assessment.

Science.gov (United States)

Montoya-Mayor, R; Fernández-Espinosa, A J; Seijo-Delgado, I; Ternero-Rodríguez, M

2013-08-01

The present work investigates the relationships between composition of rainwater and dry deposition fluxes by trace metals and metalloids. A modification in automatic "wet-only" and "dry-only" samplers was applied, which allowed the collection and conservation of samples separately. ICP-MS technique was used for the determination of analytes in samples. Concentrations of soluble elements in rainwater were measured directly in filtered samples. A sequential acid treatment with nitric, hydrofluoric and finally perchloric acids was used to measure the total contents of metals and metalloids in coarse particles. Variation between periods of heavy and light rains was assessed. Almost all of the metals and metalloids - B, Tl, Th, U, Al, Cs, Be, Ti and others - studied in dry deposition showed important decreases in concentrations (40-92%) during periods of heavy rainfall. Most of these metals and metalloids - As, Cr, Co, Ni - presented their highest levels (53-90%) in heavy rainfall periods in rainwater samples. Sources were identified in both types of samples collected using a new chemometric tool (SPCA). Urban traffic, surrounding contaminated soils and local anthropogenic sources were identified for rainwater samples. Natural and contaminated soils and general anthropogenic emissions were the sources identified for dry deposition fluxes. Copyright © 2013 Elsevier Ltd. All rights reserved.

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)

Study of antiproton flux of atmospheric origin in neighbourhood of the earth

International Nuclear Information System (INIS)

Huang, Ching-Yuan

2002-01-01

Secondary atmospheric antiprotons are studied. A parametrisation of the inclusive cross section for the p-bar production in p + p and p + A collisions is developed, based on the Quark Counting Rule, the Regge Phenomenology and data fitting. This parametrisation is shown to have a good agreement with experimental data for incident nucleon energy at least up to 24 GeV/n in the laboratory frame. By the analysis of the p-bar mean multiplicity distribution, this parametrisation can extend at least up to the centre of mass energy √s ∼ 25 GeV. Based on this well developed parametrisation, the Wounded Nucleon Model is applied to obtain the p-bar production cross section in A + A collisions. By including cosmic protons and α particles, the atmospheric p-bar flux at high balloon and satellite altitudes are calculated. The He-induced collisions are shown to contribute about 30 % in the total secondary atmospheric p-bar flux. It is observed that, for the search of the p-bar exotic origins such as the annihilation of supersymmetric dark matter (neutralino) and the evaporation of primordial black holes, the energy range up to E = 200 GeV/n for cosmic particles generating the secondary atmospheric p-bar production is the most important. It is shown that the secondary atmospheric p-bar flux used to correct the p-bar flux at TOA was underestimated in the previous works. In this work, the p-bar flux at TOA is then modified 10-15 % lower than the originally deduced, for the energy range E k > 1 GeV. A p-bar measurement experiment at the ground level is used to test the accuracy of secondary atmospheric p-bar production calculated by different works. The results of the BESS 1999 experiment at 2.77 km have confirmed the correctness of the present approach. At the AMS altitude, it is shown that the p-bar flux measured by AMS is almost the exact p-bar flux at TOA, with only 2-3 % of the atmospheric p-bar component. It is found that, even at very high altitudes, thousands of

Analysis of Atmospheric Nitrate Deposition in Lake Tahoe Using Multiple Oxygen Isotopes

Science.gov (United States)

McCabe, J. R.; Michalski, G. M.; Hernandez, L. P.; Thiemens, M. H.; Taylor, K.; Kendall, C.; Wankel, S. D.

2002-12-01

Lake Tahoe in the Sierra Nevada Mountain Range is world renown for its depth and water clarity bringing 2.2 million visitors per year resulting in annual revenue of \\1.6 billion from tourism. In past decades the lake has suffered from decreased water clarity (from 32 m plate depth to less than 20), which is believed to be largely the result of algae growth initiated by increased nutrient loading. Lake nutrients have also seen a shift from a nitrogen limited to a phosphorous limited system indicating a large increase in the flux of fixed nitrogen. Several sources of fixed nitrogen of have been suggested including surface runoff, septic tank seepage from ground water and deposition from the atmosphere. Bio-available nitrogen in the form of nitrate (NO_{3}$-) is a main component of this system. Recent studies have estimated that approximately 50% of the nitrogen input into the lake is of atmospheric origin (Allison et al. 2000). However, the impact and magnitude of atmospheric deposition is still one of the least understood aspects of the relationship between air and water quality in the Basin (TRPA Threshold Assessment 2002). The utility of stable isotopes as tracers of nitrate reservoirs has been shown in several studies (Bohlke et al. 1997, Kendall and McDonnell 1998, Durka et al. 1994). Stable nitrogen (δ15N) and oxygen (δ18O) isotopes have been implemented in a dual isotope approach to characterize the various nitrate sources to an ecosystem. While δ18O distinguishes between atmospheric and soil sources of nitrate, processes such as denitrification can enrich the residual nitrate in δ18O leaving a misleading atmospheric signature. The benefit of δ15N as a tracer for NO3- sources is the ability to differentiate natural soil, fertilizer, and animal or septic waste, which contain equivalent δ18O values. The recent implementation of multiple oxygen isotopes to measure Δ17O in nitrate has proven to be a more sensitive tracer of atmospheric deposition. The

Quantifying the Fluxes of Atmospherically Derived Trace Elements in the Arctic Ocean/Ice System using 7Be

Science.gov (United States)

Landing, W. M.; Kadko, D. C.; Shelley, R.; Galfond, B.

2016-02-01

Aerosol deposition is an important pathway for delivering biologically-essential and anthropogenically-derived trace elements to the Arctic Ocean. Limited field study in the harsh Arctic environment has forced a reliance on poorly constrained models for the atmospheric deposition of trace elements. Here we use the cosmic ray produced radioisotope 7Be to link aerosol concentrations to flux to the Arctic water/ice system. Seawater, ice, snow, melt pond, and aerosol samples were collected during late summer 2011 as part of the RV Polarstern ARK-XXVI/3 campaign. The average 7Be aerosol loading was 0.018 dpm m-3 and we determined an average 7Be flux of 125 dpm m-2 d-1, consistent with results from previous studies in the region. None of the lithogenic aerosol elements showed any significant enrichment above crustal composition, while the pollution-type elements showed varying degrees of enrichment relative to crustal values. In addition to our own measurements, we use two years of continuous aerosol 7Be and trace element data from the Alert (Canada) monitoring site to generate seasonal and annual estimates for the fluxes of 7Be and trace elements to the Arctic water/ice system. Fluxes of 7Be are 30% higher in Winter (Nov-May) than in Summer (Jun-Oct) due to the strong seasonality in aerosol 7Be concentrations. Fluxes of lithogenic elements (Al, Mn, Fe) are 2-3 times higher in Summer, possibly due to local dust sources on Ellesmere Island. Fluxes of V and Pb are strongly correlated and are 2-3 times higher in Winter, while fluxes of Ni, Cu, and Zn are relatively uniform for both seasons.

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....

Free atmospheric phosphine concentrations and fluxes in different wetland ecosystems, China

International Nuclear Information System (INIS)

Han Chao; Geng Jinju; Hong Yuning; Zhang Rui; Gu Xueyuan; Wang Xiaorong; Gao Shixiang; Glindemann, Dietmar

2011-01-01

Atmospheric phosphine (PH 3 ) fluxes from typical types of wetlands and PH 3 concentrations in adjacent atmospheric air were measured. The seasonal distribution of PH 3 in marsh and paddy fields were observed. Positive PH 3 fluxes are significantly related to high air temperature (summer season) and increased vegetation. It is concluded that vegetation speeds up the liberation of PH 3 from soils, while water coverage might function as a diffusion barrier from soils or sediments to the atmosphere. The concentrations of atmospheric PH 3 (ng m -3 ) above different wetlands decrease in the order of paddy fields (51.8 ± 3.1) > marsh (46.5 ± 20.5) > lake (37.0 ± 22.7) > coastal wetland (1.71 ± 0.73). Highest atmospheric PH 3 levels in marsh are found in summer. In paddy fields, atmospheric PH 3 concentrations in flourishing stages are higher than those in slowly growing stages. - Research highlights: → P could migrate as PH 3 gas in different wetland ecosystems. → Wetlands act as a source and sink of atmospheric PH 3 . → Positive PH 3 fluxes are significantly related to high temperature and increased vegetation. → Environmental PH 3 concentrations in China are generally higher. - Environmental PH 3 concentrations in China are generally higher compared to other parts of the world.

A new calculation of atmospheric neutrino flux: the FLUKA approach

International Nuclear Information System (INIS)

Battistoni, G.; Bloise, C.; Cavalli, D.; Ferrari, A.; Montaruli, T.; Rancati, T.; Resconi, S.; Ronga, F.; Sala, P.R.

1999-01-01

Preliminary results from a full 3-D calculation of atmospheric neutrino fluxes using the FLUKA interaction model are presented and compared to previous existing calculations. This effort is motivated mainly by the 3-D capability and the satisfactory degree of accuracy of the hadron-nucleus models embedded in the FLUKA code. Here we show examples of benchmarking tests of the model with cosmic ray experiment results. A comparison of our calculation of the atmospheric neutrino flux with that of the Bartol group, for E ν > 1 GeV, is presented

Experimental study of the atmospheric neutrino flux

International Nuclear Information System (INIS)

Hirata, K.S.; Kajita, T.; Koshiba, M.

1988-01-01

We have observed 277 fully contained events in the KAMIOKANDE detector. The number of electron-like single prong events is in good agreement with the predictions of a Monte Carlo calculation based on atmospheric neutrino interactions in the detector. On the other hand, the number of muon-like single prong events is 59 ± 7 %(statistical error) of the predicted number of the Monte Carlo calculation. We are unable to explain the data as the result of systematic detector effects or uncertainties in the atmospheric neutrino fluxes. (author)

Decadal trends in atmospheric deposition in a high elevation station: Effects of climate and pollution on the long-range flux of metals and trace elements over SW Europe

Science.gov (United States)

Camarero, Lluís; Bacardit, Montserrat; de Diego, Alberto; Arana, Gorka

2017-10-01

Atmospheric deposition collected at remote, high elevation stations is representative of long-range transport of elements. Here we present time-series of Al, Fe, Ti, Mn, Zn, Ni, Cu, As, Cd and Pb deposition sampled in the Central Pyrenees at 2240 m a.s.l, representative of the fluxes of these elements over South West Europe. Trace element deposition did not show a simple trend. Rather, there was statistical evidence of several underlying factors governing the variability of the time-series recorded: seasonal cycles, trends, the effects of the amount of precipitation, climate-controlled export of dust, and changes in anthropogenic emissions. Overall, there were three main modes of variation in deposition. The first mode was related to North Atlantic Oscillation (NAO), and affected Al, Fe, Ti, Mn and Pb. We interpret this as changes in the dust export from Northern Africa under the different meteorological conditions that the NAO index indicates. The second mode was an upward trend related to a rise in the frequency of precipitation events (that also lead to an increase in the amount). More frequent events might cause a higher efficiency in the scavenging of aerosols. As, Cu and Ni responded to this. And finally, the third mode of variation was related to changes in anthropogenic emissions of Pb and Zn.

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

The prompt atmospheric neutrino flux in the light of LHCb

International Nuclear Information System (INIS)

Gauld, Rhorry; Rojo, Juan; Rottoli, Luca; Sarkar, Subir; Talbert, Jim

2016-01-01

The recent observation of very high energy cosmic neutrinos by IceCube heralds the beginning of neutrino astronomy. At these energies, the dominant background to the astrophysical signal is the flux of ‘prompt’ neutrinos, arising from the decay of charmed mesons produced by cosmic ray collisions in the atmosphere. In this work we provide predictions for the prompt atmospheric neutrino flux in the framework of perturbative QCD, using state-of-the-art Monte Carlo event generators. Our calculation includes the constraints set by charm production measurements from the LHCb experiment at 7 TeV, recently validated with the corresponding 13 TeV data. Our result for the prompt flux is a factor of about 2 below the previous benchmark calculation, in general agreement with other recent estimates, but with an improved estimate of the uncertainty. This alleviates the existing tension between the theoretical prediction and IceCube limits, and suggests that a direct detection of the prompt flux is imminent.

Modelling stomatal ozone flux and deposition to grassland communities across Europe

International Nuclear Information System (INIS)

Ashmore, M.R.; Bueker, P.; Emberson, L.D.; Terry, A.C.; Toet, S.

2007-01-01

Regional scale modelling of both ozone deposition and the risk of ozone impacts is poorly developed for grassland communities. This paper presents new predictions of stomatal ozone flux to grasslands at five different locations in Europe, using a mechanistic model of canopy development for productive grasslands to generate time series of leaf area index and soil water potential as inputs to the stomatal component of the DO 3 SE ozone deposition model. The parameterisation of both models was based on Lolium perenne, a dominant species of productive pasture in Europe. The modelled seasonal time course of stomatal ozone flux to both the whole canopy and to upper leaves showed large differences between climatic zones, which depended on the timing of the start of the growing season, the effect of soil water potential, and the frequency of hay cuts. Values of modelled accumulated flux indices and the AOT40 index showed a five-fold difference between locations, but the locations with the highest flux differed depending on the index used; the period contributing to the accumulation of AOT40 did not always coincide with the modelled period of active ozone canopy uptake. Use of a fixed seasonal profile of leaf area index in the flux model produced very different estimates of annual accumulated total canopy and leaf ozone flux when compared with the flux model linked to a simulation of canopy growth. Regional scale model estimates of both the risks of ozone impacts and of total ozone deposition will be inaccurate unless the effects of climate and management in modifying grass canopy growth are incorporated. - Modelled stomatal flux of ozone to productive grasslands in Europe shows different spatial and temporal variation to AOT40, and is modified by management and soil water status

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)

Determination of lead 210 atmospheric fluxes in Syria

International Nuclear Information System (INIS)

Al-Masri, M. S.; Shaik Khalil, H.

2001-01-01

Lead 210 atmospheric fluxes were determined by collecting 51 profiles from Syrian soil during 1998. Lead 210 fluxes in Syria calculated from lead 210 inventory in soil ranged from 15 Bq.m -2 .y -1 and 407 Bq.m -2 .y -1 with an average value of 128 Bq.m -2 .y -1 . the highest fluxes were found to be in Hama area due to the Gaab fault, which is considered as a radon source in the area. In addition, fluxes were also high in most sites, which are located in Syria valleys and around the lakes. Moreover, the study has indicated that there is no linear relation between lead 210 flux values and other parameters such as annual rainfall and bulk density of the soil. On the other hand, an effect, of those two factors on lead 210 distribution with depth has been observed. In addition, the results of variable lead 210 fluxes from site to another have proved that it is necessary, in order to obtain a representative mean value of lead 210 flux obtained in this study is within the worldwide range for lead 210 flux. (Author)

Study of cosmic ray interaction model based on atmospheric muons for the neutrino flux calculation

International Nuclear Information System (INIS)

Sanuki, T.; Honda, M.; Kajita, T.; Kasahara, K.; Midorikawa, S.

2007-01-01

We have studied the hadronic interaction for the calculation of the atmospheric neutrino flux by summarizing the accurately measured atmospheric muon flux data and comparing with simulations. We find the atmospheric muon and neutrino fluxes respond to errors in the π-production of the hadronic interaction similarly, and compare the atmospheric muon flux calculated using the HKKM04 [M. Honda, T. Kajita, K. Kasahara, and S. Midorikawa, Phys. Rev. D 70, 043008 (2004).] code with experimental measurements. The μ + +μ - data show good agreement in the 1∼30 GeV/c range, but a large disagreement above 30 GeV/c. The μ + /μ - ratio shows sizable differences at lower and higher momenta for opposite directions. As the disagreements are considered to be due to assumptions in the hadronic interaction model, we try to improve it phenomenologically based on the quark parton model. The improved interaction model reproduces the observed muon flux data well. The calculation of the atmospheric neutrino flux will be reported in the following paper [M. Honda et al., Phys. Rev. D 75, 043006 (2007).

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

Simultaneous coastal measurements of ozone deposition fluxes and iodine-mediated particle emission fluxes with subsequent CCN formation

Directory of Open Access Journals (Sweden)

J. D. Whitehead

2010-01-01

Full Text Available Here we present the first observations of simultaneous ozone deposition fluxes and ultrafine particle emission fluxes over an extensive infra-littoral zone. Fluxes were measured by the eddy covariance technique at the Station Biologique de Roscoff, on the coast of Brittany, north-west France. This site overlooks a very wide (3 km littoral zone controlled by very deep tides (9.6 m exposing extensive macroalgae beds available for significant iodine mediated photochemical production of ultrafine particles. The aspect at the Station Biologique de Roscoff provides an extensive and relatively flat, uniform fetch within which micrometeorological techniques may be utilized to study links between ozone deposition to macroalgae (and sea water and ultrafine particle production.

Ozone deposition to seawater at high tide was significantly slower (v_d[O₃]=0.302±0.095 mm s⁻¹ than low tidal deposition. A statistically significant difference in the deposition velocities to macroalgae at low tide was observed between night time (v_d[O₃]=1.00±0.10 mm s⁻¹ and daytime (v_d[O₃]=2.05±0.16 mm s⁻¹ when ultrafine particle formation results in apparent particle emission. Very high emission fluxes of ultrafine particles were observed during daytime periods at low tides ranging from 50 000 particles cm⁻² s⁻¹ to greater than 200 000 particles cm⁻² s⁻¹ during some of the lowest tides. These emission fluxes exhibited a significant relationship with particle number concentrations comparable with previous observations at another location. Apparent particle growth rates were estimated to be in the range 17–150 nm h⁻¹ for particles in the size range 3–10 nm. Under certain conditions, particle growth may be inferred to continue to greater than 120 nm over tens

Experimentally guided Monte Carlo calculations of the atmospheric muon flux for interdisciplinary applications

International Nuclear Information System (INIS)

Mitrica, B.; Brancus, I.M.; Toma, G.; Bercuci, A.; Aiftimiei, C.; Wentz, J.; Rebel, H.

2004-01-01

Atmospheric muons are produced in the interactions of primary cosmic rays particle with Earth's atmosphere, mainly by the decay of pions and kaons generated in hadronic interactions. They decay further in electrons and positrons and electron and muon neutrinos. Being the penetrating cosmic rays component, the muons manage to pass entirely through the atmosphere and can pass even larger absorbers before they interact with the material at the Earth's surface, and due to cosmogenic production of isotopes by atmospheric muons, information of astrophysical, environmental and material research interest can be obtained. Up to now, mainly semi-analytical approximations have been used to calculate the muon flux for estimating the cosmogenic isotope production, necessary for different applications. Our estimation of the atmospheric muon flux is based on a Monte-Carlo simulation program CORSIKA, in which we simulate the development in the atmosphere of the extensive air showers, using different models for the description of the hadronic interaction. Atmospheric muons are produced in the interactions of primary cosmic rays particle with Earth's atmosphere, mainly by the decay of pions and kaons generated in hadronic interactions. They decay further in electrons and positrons and electron and muon neutrinos. Being the penetrating cosmic rays component, the muons manage to pass entirely through the atmosphere and can pass even larger absorbers before they interact with the material at the Earth's surface, and due to cosmogenic production of isotopes by atmospheric muons, information of astrophysical, environmental and material research interest can be obtained. Up to now, mainly semi-analytical approximations have been used to calculate the muon flux for estimating the cosmogenic isotope production, necessary for different applications. Our estimation of the atmospheric muon flux is based on a Monte-Carlo simulation program CORSIKA, in which we simulates the development in the

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.

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

Role of plasma enhanced atomic layer deposition reactor wall conditions on radical and ion substrate fluxes

Energy Technology Data Exchange (ETDEWEB)

Sowa, Mark J., E-mail: msowa@ultratech.com [Ultratech/Cambridge NanoTech, 130 Turner Street, Building 2, Waltham, Massachusetts 02453 (United States)

2014-01-15

Chamber wall conditions, such as wall temperature and film deposits, have long been known to influence plasma source performance on thin film processing equipment. Plasma physical characteristics depend on conductive/insulating properties of chamber walls. Radical fluxes depend on plasma characteristics as well as wall recombination rates, which can be wall material and temperature dependent. Variations in substrate delivery of plasma generated species (radicals, ions, etc.) impact the resulting etch or deposition process resulting in process drift. Plasma enhanced atomic layer deposition is known to depend strongly on substrate radical flux, but film properties can be influenced by other plasma generated phenomena, such as ion bombardment. In this paper, the chamber wall conditions on a plasma enhanced atomic layer deposition process are investigated. The downstream oxygen radical and ion fluxes from an inductively coupled plasma source are indirectly monitored in temperature controlled (25–190 °C) stainless steel and quartz reactors over a range of oxygen flow rates. Etch rates of a photoresist coated quartz crystal microbalance are used to study the oxygen radical flux dependence on reactor characteristics. Plasma density estimates from Langmuir probe ion saturation current measurements are used to study the ion flux dependence on reactor characteristics. Reactor temperature was not found to impact radical and ion fluxes substantially. Radical and ion fluxes were higher for quartz walls compared to stainless steel walls over all oxygen flow rates considered. The radical flux to ion flux ratio is likely to be a critical parameter for the deposition of consistent film properties. Reactor wall material, gas flow rate/pressure, and distance from the plasma source all impact the radical to ion flux ratio. These results indicate maintaining chamber wall conditions will be important for delivering consistent results from plasma enhanced atomic layer deposition

Intercomparison of oceanic and atmospheric forced and coupled mesoscale simulations Part I: Surface fluxes

Directory of Open Access Journals (Sweden)

P. Josse

1999-04-01

Full Text Available A mesoscale non-hydrostatic atmospheric model has been coupled with a mesoscale oceanic model. The case study is a four-day simulation of a strong storm event observed during the SEMAPHORE experiment over a 500 × 500 km2 domain. This domain encompasses a thermohaline front associated with the Azores current. In order to analyze the effect of mesoscale coupling, three simulations are compared: the first one with the atmospheric model forced by realistic sea surface temperature analyses; the second one with the ocean model forced by atmospheric fields, derived from weather forecast re-analyses; the third one with the models being coupled. For these three simulations the surface fluxes were computed with the same bulk parametrization. All three simulations succeed well in representing the main oceanic or atmospheric features observed during the storm. Comparison of surface fields with in situ observations reveals that the winds of the fine mesh atmospheric model are more realistic than those of the weather forecast re-analyses. The low-level winds simulated with the atmospheric model in the forced and coupled simulations are appreciably stronger than the re-analyzed winds. They also generate stronger fluxes. The coupled simulation has the strongest surface heat fluxes: the difference in the net heat budget with the oceanic forced simulation reaches on average 50 Wm-2 over the simulation period. Sea surface-temperature cooling is too weak in both simulations, but is improved in the coupled run and matches better the cooling observed with drifters. The spatial distributions of sea surface-temperature cooling and surface fluxes are strongly inhomogeneous over the simulation domain. The amplitude of the flux variation is maximum in the coupled run. Moreover the weak correlation between the cooling and heat flux patterns indicates that the surface fluxes are not responsible for the whole cooling and suggests that the response of the ocean mixed layer

Intercomparison of oceanic and atmospheric forced and coupled mesoscale simulations Part I: Surface fluxes

Directory of Open Access Journals (Sweden)

H. Giordani

Full Text Available A mesoscale non-hydrostatic atmospheric model has been coupled with a mesoscale oceanic model. The case study is a four-day simulation of a strong storm event observed during the SEMAPHORE experiment over a 500 × 500 km2 domain. This domain encompasses a thermohaline front associated with the Azores current. In order to analyze the effect of mesoscale coupling, three simulations are compared: the first one with the atmospheric model forced by realistic sea surface temperature analyses; the second one with the ocean model forced by atmospheric fields, derived from weather forecast re-analyses; the third one with the models being coupled. For these three simulations the surface fluxes were computed with the same bulk parametrization. All three simulations succeed well in representing the main oceanic or atmospheric features observed during the storm. Comparison of surface fields with in situ observations reveals that the winds of the fine mesh atmospheric model are more realistic than those of the weather forecast re-analyses. The low-level winds simulated with the atmospheric model in the forced and coupled simulations are appreciably stronger than the re-analyzed winds. They also generate stronger fluxes. The coupled simulation has the strongest surface heat fluxes: the difference in the net heat budget with the oceanic forced simulation reaches on average 50 Wm-2 over the simulation period. Sea surface-temperature cooling is too weak in both simulations, but is improved in the coupled run and matches better the cooling observed with drifters. The spatial distributions of sea surface-temperature cooling and surface fluxes are strongly inhomogeneous over the simulation domain. The amplitude of the flux variation is maximum in the coupled run. Moreover the weak correlation between the cooling and heat flux patterns indicates that the surface fluxes are not responsible for the whole cooling and suggests that the response of the ocean mixed layer

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...

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)

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, 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)

Heavy metal deposition fluxes affecting an Atlantic coastal area in the southwest of Spain

Science.gov (United States)

Castillo, Sonia; de la Rosa, Jesús D.; Sánchez de la Campa, Ana M.; González-Castanedo, Yolanda; Fernández-Camacho, Rocío

2013-10-01

The present study seeks to estimate the impact of industrial emissions and harbour activities on total atmospheric deposition in an Atlantic coastal area in the southwest of the Iberian Peninsula. Three large industrial estates and a busy harbour have a notable influence on air quality in the city of Huelva and the surrounding area. The study is based on a geochemical characterization of trace elements deposited (soluble and insoluble fractions) in samples collected at a rate of 15 days/sample from June 2008 to May 2011 in three sampling sites, one in the principal industrial belt, another in the city of Huelva, and the last, 56 km outside Huelva city in an area of high ecological interest. The industrial emissions emitted by the Huelva industrial belt exert a notable influence on atmospheric deposition. Major deposition fluxes were registered for Fe, Cu, V, Ni, P, Pb, As, Sn, Sb, Se and Bi, principally in the insoluble fraction, derived from industrial funnel emissions and from harbour activities. Metals such as Mn, Ni, Cu and Zn, and elements such as P also have a significant presence in the soluble fraction converting them into potentially bio-available nutrients for the living organism in the ocean. A principal component analysis certifies three common emissions sources in the area: 1) a mineral factor composed mainly of elements derived from silicate minerals mixed with certain anthropogenic species (Mg, K, Sr, Na, Al, Ba, LREE, Li, Mn, HREE, Ti, Fe, Se, V, SO-, Ni, Ca and P); 2) an industrial factor composed of the same trace elements in the three areas (Sb, Mo, Bi, As, Pb, Sn and Cd) thus confirming the impact of the emissions from the Huelva industrial belt on remote areas; and 3) a marine factor composed of Na, Cl, Mg and SO.

Intercomparison of oceanic and atmospheric forced and coupled mesoscale simulations. Part I: Surface fluxes

Science.gov (United States)

Josse, P.; Caniaux, G.; Giordani, H.; Planton, S.

1999-04-01

A mesoscale non-hydrostatic atmospheric model has been coupled with a mesoscale oceanic model. The case study is a four-day simulation of a strong storm event observed during the SEMAPHORE experiment over a 500 × 500 km2 domain. This domain encompasses a thermohaline front associated with the Azores current. In order to analyze the effect of mesoscale coupling, three simulations are compared: the first one with the atmospheric model forced by realistic sea surface temperature analyses; the second one with the ocean model forced by atmospheric fields, derived from weather forecast re-analyses; the third one with the models being coupled. For these three simulations the surface fluxes were computed with the same bulk parametrization. All three simulations succeed well in representing the main oceanic or atmospheric features observed during the storm. Comparison of surface fields with in situ observations reveals that the winds of the fine mesh atmospheric model are more realistic than those of the weather forecast re-analyses. The low-level winds simulated with the atmospheric model in the forced and coupled simulations are appreciably stronger than the re-analyzed winds. They also generate stronger fluxes. The coupled simulation has the strongest surface heat fluxes: the difference in the net heat budget with the oceanic forced simulation reaches on average 50 Wm-2 over the simulation period. Sea surface-temperature cooling is too weak in both simulations, but is improved in the coupled run and matches better the cooling observed with drifters. The spatial distributions of sea surface-temperature cooling and surface fluxes are strongly inhomogeneous over the simulation domain. The amplitude of the flux variation is maximum in the coupled run. Moreover the weak correlation between the cooling and heat flux patterns indicates that the surface fluxes are not responsible for the whole cooling and suggests that the response of the ocean mixed layer to the atmosphere is

Greenhouse gases regional fluxes estimated from atmospheric measurements

International Nuclear Information System (INIS)

Messager, C.

2007-07-01

build up a new system to measure continuously CO 2 (or CO), CH 4 , N 2 O and SF 6 mixing ratios. It is based on a commercial gas chromatograph (Agilent 6890N) which have been modified to reach better precision. Reproducibility computed with a target gas on a 24 hours time step gives: 0.06 ppm for CO 2 , 1.4 ppb for CO, 0.7 ppb for CH 4 , 0.2 ppb for N 2 O and 0.05 ppt for SF 6 . The instrument's run is fully automated, an air sample analysis takes about 5 minutes. In July 2006, I install instrumentation on a telecommunication tall tower (200 m) situated near Orleans forest in Trainou, to monitor continuously greenhouse gases (CO 2 , CH 4 , N 2 O, SF 6 ), atmospheric tracers (CO, Radon-222) and meteorological parameters. Intake lines were installed at 3 levels (50, 100 and 180 m) and allow us to sample air masses along the vertical. Continuous measurement started in January 2007. I used Mace Head (Ireland) and Gif-sur-Yvette continuous measurements to estimate major greenhouse gases emission fluxes at regional scale. To make the link between atmospheric measurements and surface fluxes, we need to quantify dilution due to atmospheric transport. I used Radon-222 as tracer (radon tracer method) and planetary boundary layer heights estimates from ECMWF model (boundary layer budget method) to parameterize atmospheric transport. In both cases I compared results to available emission inventories. (author)

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)

Study of heat flux deposition in the Tore Supra Tokamak

International Nuclear Information System (INIS)

Carpentier, S.

2009-02-01

Accurate measurements of heat loads on internal tokamak components is essential for protection of the device during steady state operation. The optimisation of experimental scenarios also requires an in depth understanding of the physical mechanisms governing the heat flux deposition on the walls. The objective of this study is a detailed characterisation of the heat flux to plasma facing components (PFC) of the Tore Supra tokamak. The power deposited onto Tore Supra PFCs is calculated using an inverse method, which is applied to both the temperature maps measured by infrared thermography and to the enthalpy signals from calorimetry. The derived experimental heat flux maps calculated on the toroidal pumped limiter (TPL) are then compared with theoretical heat flux density distributions from a standard SOL-model. They are two experimental observations that are not consistent with the model: significant heat flux outside the theoretical wetted area, and heat load peaking close to the tangency point between the TPL and the last closed field surface (LCFS). An experimental analysis for several discharges with variable security factors q is made. In the area consistent with the theoretical predictions, this parametric study shows a clear dependence between the heat flux length λ q (estimated in the SOL (scrape-off layer) from the IR measurements) and the magnetic configuration. We observe that the spreading of heat fluxes on the component is compensated by a reduction of the power decay length λ q in the SOL when q decreases. On the other hand, in the area where the derived experimental heat loads are not consistent with the theoretical predictions, we observe that the spreading of heat fluxes outside the theoretical boundary increases when q decreases, and is thus not counterbalanced. (author)

Critical loads of nitrogen deposition and critical levels of atmospheric ammonia for semi-natural Mediterranean evergreen woodlands

Directory of Open Access Journals (Sweden)

P. Pinho

2012-03-01

Full Text Available Nitrogen (N has emerged in recent years as a key factor associated with global changes, with impacts on biodiversity, ecosystems functioning and human health. In order to ameliorate the effects of excessive N, safety thresholds such as critical loads (deposition fluxes and levels (concentrations can be established. Few studies have assessed these thresholds for semi-natural Mediterranean ecosystems. Our objective was therefore to determine the critical loads of N deposition and long-term critical levels of atmospheric ammonia for semi-natural Mediterranean evergreen woodlands. We have considered changes in epiphytic lichen communities, one of the most sensitive comunity indicators of excessive N in the atmosphere. Based on a classification of lichen species according to their tolerance to N we grouped species into response functional groups, which we used as a tool to determine the critical loads and levels. This was done for a Mediterranean climate in evergreen cork-oak woodlands, based on the relation between lichen functional diversity and modelled N deposition for critical loads and measured annual atmospheric ammonia concentrations for critical levels, evaluated downwind from a reduced N source (a cattle barn. Modelling the highly significant relationship between lichen functional groups and annual atmospheric ammonia concentration showed the critical level to be below 1.9 μg m⁻³, in agreement with recent studies for other ecosystems. Modelling the highly significant relationship between lichen functional groups and N deposition showed that the critical load was lower than 26 kg (N ha⁻¹ yr⁻¹, which is within the upper range established for other semi-natural ecosystems. Taking into account the high sensitivity of lichen communities to excessive N, these values should aid development of policies to protect Mediterranean woodlands from the initial effects of excessive N.

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)

A decade of monitoring at Swiss Long-Term Forest Ecosystem Research (LWF) sites: can we observe trends in atmospheric acid deposition and in soil solution acidity?

Science.gov (United States)

Pannatier, Elisabeth Graf; Thimonier, Anne; Schmitt, Maria; Walthert, Lorenz; Waldner, Peter

2011-03-01

Trends in atmospheric acid deposition and in soil solution acidity from 1995 or later until 2007 were investigated at several forest sites throughout Switzerland to assess the effects of air pollution abatements on deposition and the response of the soil solution chemistry. Deposition of the major elements was estimated from throughfall and bulk deposition measurements at nine sites of the Swiss Long-Term Forest Ecosystem Research network (LWF) since 1995 or later. Soil solution was measured at seven plots at four soil depths since 1998 or later. Trends in the molar ratio of base cations to aluminum (BC/Al) in soil solutions and in concentrations and fluxes of inorganic N (NO(3)-N + NH(4)-N), sulfate (SO(4)-S), and base cations (BC) were used to detect changes in soil solution chemistry. Acid deposition significantly decreased at three out of the nine study sites due to a decrease in total N deposition. Total SO(4)-S deposition decreased at the nine sites, but due to the relatively low amount of SO(4)-S load compared to N deposition, it did not contribute to decrease acid deposition significantly. No trend in total BC deposition was detected. In the soil solution, no trend in concentrations and fluxes of BC, SO(4)-S, and inorganic N were found at most soil depths at five out of the seven sites. This suggests that the soil solution reacted very little to the changes in atmospheric deposition. A stronger reduction in base cations compared to aluminum was detected at two sites, which might indicate that acidification of the soil solution was proceeding faster at these sites.

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.

VALDRIFT 1.0: A valley atmospheric dispersion model with deposition

Energy Technology Data Exchange (ETDEWEB)

Allwine, K.J.; Bian, X.; Whiteman, C.D.

1995-05-01

VALDRIFT version 1.0 is an atmospheric transport and diffusion model for use in well-defined mountain valleys. It is designed to determine the extent of ddft from aedal pesticide spraying activities, but can also be applied to estimate the transport and diffusion of various air pollutants in valleys. The model is phenomenological -- that is, the dominant meteorological processes goveming the behavior of the valley atmosphere are formulated explicitly in the model, albeit in a highly parameterized fashion. The key meteorological processes treated are: (1) nonsteady and nonhomogeneous along-valley winds and turbulent diffusivities, (2) convective boundary layer growth, (3) inversion descent, (4) noctumal temperature inversion breakup, and (5) subsidence. The model is applicable under relatively cloud-free, undisturbed synoptic conditions and is configured to operate through one diumal cycle for a single valley. The inputs required are the valley topographical characteristics, pesticide release rate as a function of time and space, along-valley wind speed as a function of time and space, temperature inversion characteristics at sunrise, and sensible heat flux as a function of time following sunrise. Default values are provided for certain inputs in the absence of detailed observations. The outputs are three-dimensional air concentration and ground-level deposition fields as a function of time.

Size-resolved fluxes of sub-100-nm particles over forests

DEFF Research Database (Denmark)

Pryor, Sara; Barthelmie, Rebecca Jane; Spaulding, A.M.

2009-01-01

Dry deposition of atmospheric particles is critically dependent on particle size and plays a key role in dictating the mass and number distributions of atmospheric particles. However, modeling dry deposition is constrained by a lack of understanding of controlling dependencies and accurate size......-resolved observations. We present size-resolved particle number fluxes for sub-100-nm particle diameters (Dp) over a deciduous forest derived using eddy covariance applied to data from a fast mobility particle sizer. The size-resolved particle number fluxes in 18 diameters between 8 and 100 nm were collected during...... leaf-on and are statistically robust. Particle deposition velocities normalized by friction velocity (v d +) are approximately four times smaller than comparable values for coniferous forests reported elsewhere. Comparison of the data with output from a new one-dimensional mechanistic particle...

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 .

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...

Improvement of low energy atmospheric neutrino flux calculation using the JAM nuclear interaction model

International Nuclear Information System (INIS)

Honda, M.; Kajita, T.; Kasahara, K.; Midorikawa, S.

2011-01-01

We present the calculation of the atmospheric neutrino fluxes with an interaction model named JAM, which is used in PHITS (Particle and Heavy-Ion Transport code System) [K. Niita et al., Radiation Measurements 41, 1080 (2006).]. The JAM interaction model agrees with the HARP experiment [H. Collaboration, Astropart. Phys. 30, 124 (2008).] a little better than DPMJET-III[S. Roesler, R. Engel, and J. Ranft, arXiv:hep-ph/0012252.]. After some modifications, it reproduces the muon flux below 1 GeV/c at balloon altitudes better than the modified DPMJET-III, which we used for the calculation of atmospheric neutrino flux in previous works [T. Sanuki, M. Honda, T. Kajita, K. Kasahara, and S. Midorikawa, Phys. Rev. D 75, 043005 (2007).][M. Honda, T. Kajita, K. Kasahara, S. Midorikawa, and T. Sanuki, Phys. Rev. D 75, 043006 (2007).]. Some improvements in the calculation of atmospheric neutrino flux are also reported.

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

Multi-model Mean Nitrogen and Sulfur Deposition from the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP): Evaluation Historical and Projected Changes

Science.gov (United States)

Lamarque, J.-F.; Dentener, F.; McConnell, J.; Ro, C.-U.; Shaw, M.; Vet, R.; Bergmann, D.; Cameron-Smith, P.; Doherty, R.; Faluvegi, G.;

Patterns of Precipitation and Streamflow Responses to Moisture Fluxes during Atmospheric Rivers

Science.gov (United States)

Henn, B. M.; Wilson, A. M.; Asgari Lamjiri, M.; Ralph, M.

2017-12-01

Precipitation from landfalling atmospheric rivers (ARs) have been shown to dominate the hydroclimate of many parts of the world. ARs are associated with saturated, neutrally-stable profiles in the lower atmosphere, in which forced ascent by topography induces precipitation. Understanding the spatial and temporal variability of precipitation over complex terrain during AR-driven precipitation is critical for accurate forcing of distributed hydrologic models and streamflow forecasts. Past studies using radar wind profilers and radiosondes have demonstrated predictability of precipitation rates based on upslope water vapor flux over coastal terrain, with certain levels of moisture flux exhibiting the greatest influence on precipitation. Additionally, these relationships have been extended to show that streamflow in turn responds predictably to upslope vapor flux. However, past studies have focused on individual pairs of profilers and precipitation gauges; the question of how orographic precipitation in ARs is distributed spatially over complex terrain, at different topographic scales, is less well known. Here, we examine profiles of atmospheric moisture transport from radiosondes and wind profilers, against a relatively dense network of precipitation gauges, as well as stream gauges, to assess relationships between upslope moisture flux and the spatial response of precipitation and streamflow. We focus on California's Russian River watershed in the 2016-2017 cool season, when regular radiosonde launches were made at two locations during an active sequence of landfalling ARs. We examine how atmospheric water vapor flux results in precipitation patterns across gauges with different topographic relationships to the prevailing moisture-bearing winds, and conduct a similar comparison of runoff volume response from several unimpaired watersheds in the upper Russian watershed, taking into account antecedent soil moisture conditions that influence runoff generation. Finally

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

Multi-model Mean Nitrogen and Sulfur Deposition from the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP): Evaluation of Historical and Projected Future Changes

Energy Technology Data Exchange (ETDEWEB)

Lamarque, Jean-Francois; Dentener, Frank; McConnell, J.R.; Ro, C-U; Shaw, Mark; Vet, Robert; Bergmann, D.; Cameron-Smith, Philip; Dalsoren, S.; Doherty, R.; Faluvegi, G.; Ghan, Steven J.; Josse, B.; Lee, Y. H.; MacKenzie, I. A.; Plummer, David; Shindell, Drew; Skeie, R. B.; Stevenson, D. S.; Strode, S.; Zeng, G.; Curran, M.; Dahl-Jensen, D.; Das, S.; Fritzsche, D.; Nolan, M.

2013-08-20

We present multi-model global datasets of nitrogen and sulfate deposition covering time periods from 1850 to 2100, calculated within the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP). The computed deposition fluxes are compared to surface wet deposition and ice-core measurements. We use a new dataset of wet deposition for 2000-2002 based on critical assessment of the quality of existing regional network data. We show that for present-day (year 2000 ACCMIP time-slice), the ACCMIP results perform similarly to previously published multi-model assessments. The analysis of changes between 1980 and 2000 indicates significant differences between model and measurements over the United States, but less so over Europe. This difference points towards misrepresentation of 1980 NH3 emissions over North America. Based on ice-core records, the 1850 deposition fluxes agree well with Greenland ice cores but the change between 1850 and 2000 seems to be overestimated in the Northern Hemisphere for both nitrogen and sulfur species. Using the Representative Concentration Pathways to define the projected climate and atmospheric chemistry related emissions and concentrations, we find large regional nitrogen deposition increases in 2100 in Latin America, Africa and parts of Asia under some of the scenarios considered. Increases in South Asia are especially large, and are seen in all scenarios, with 2100 values more than double 2000 in some scenarios and reaching >1300 mgN/m2/yr averaged over regional to continental scale regions in RCP 2.6 and 8.5, ~30-50% larger than the values in any region currently (2000). Despite known issues, the new ACCMIP deposition dataset provides novel, consistent and evaluated global gridded deposition fields for use in a wide range of climate and ecological studies.

Historical deposition and fluxes of mercury in Narraguinnep Reservoir, southwestern Colorado, USA

International Nuclear Information System (INIS)

Gray, John E.; Fey, David L.; Holmes, Charles W.; Lasorsa, Brenda K.

2005-01-01

Narraguinnep Reservoir has been identified as containing fish with elevated Hg concentrations and has been posted with an advisory recommending against consumption of fish. There are presently no point sources of significant Hg contamination to this reservoir or its supply waters. To evaluate potential historical Hg sources and deposition of Hg to Narraguinnep Reservoir, the authors measured Hg concentrations in sediment cores collected from this reservoir. The cores were dated by the 137 Cs method and these dates were further refined by relating water supply basin hydrological records with core sedimentology. Rates of historical Hg flux were calculated (ng/cm 2 /a) based on the Hg concentrations in the cores, sediment bulk densities, and sedimentation rates. The flux of Hg found in Narraguinnep Reservoir increased by approximately a factor of 2 after about 1970. The 3 most likely sources of Hg to Narraguinnep Reservoir are surrounding bedrocks, upstream inactive Au-Ag mines, and several coal-fired electric power plants in the Four Corners region. Patterns of Hg flux do not support dominant Hg derivation from surrounding bedrocks or upstream mining sources. There are 14 coal-fired power plants within 320 km of Narraguinnep Reservoir that produce over 80 x 10 6 MWH of power and about 1640 kg-Hg/a are released through stack emissions, contributing significant Hg to the surrounding environment. Two of the largest power plants, located within 80 km of the reservoir, emit about 950 kg-Hg/a. Spatial and temporal patterns of Hg fluxes for sediment cores collected from Narraguinnep Reservoir suggest that the most likely source of Hg to this reservoir is from atmospheric emissions from the coal-fired electric power plants, the largest of which began operation in this region in the late-1960s and early 1970s

Effects of elevated CO2 and nitrogen deposition on ecosystem carbon fluxes on the Sanjiang plain wetland in Northeast China.

Science.gov (United States)

Wang, Jianbo; Zhu, Tingcheng; Ni, Hongwei; Zhong, Haixiu; Fu, Xiaoling; Wang, Jifeng

2013-01-01

Increasing atmospheric CO2 and nitrogen (N) deposition across the globe may affect ecosystem CO2 exchanges and ecosystem carbon cycles. Additionally, it remains unknown how increased N deposition and N addition will alter the effects of elevated CO2 on wetland ecosystem carbon fluxes. Beginning in 2010, a paired, nested manipulative experimental design was used in a temperate wetland of northeastern China. The primary factor was elevated CO2, accomplished using Open Top Chambers, and N supplied as NH4NO3 was the secondary factor. Gross primary productivity (GPP) was higher than ecosystem respiration (ER), leading to net carbon uptake (measured by net ecosystem CO2 exchange, or NEE) in all four treatments over the growing season. However, their magnitude had interannual variations, which coincided with air temperature in the early growing season, with the soil temperature and with the vegetation cover. Elevated CO2 significantly enhanced GPP and ER but overall reduced NEE because the stimulation caused by the elevated CO2 had a greater impact on ER than on GPP. The addition of N stimulated ecosystem C fluxes in both years and ameliorated the negative impact of elevated CO2 on NEE. In this ecosystem, future elevated CO2 may favor carbon sequestration when coupled with increasing nitrogen deposition.

Dry deposition of submicron atmospheric aerosol over water surfaces in motion

International Nuclear Information System (INIS)

Nevenick, Calec

2013-01-01

Whether by chronic or accidental releases, the impact of a nuclear installation on the environment mainly depends on atmospheric transfers; and as the accidents at Chernobyl and Fukushima show, affect the contamination of surfaces and impacts in the medium and long-term on the environment and the population. In this context, this work focuses on the characterization and modeling of dry deposition of submicron aerosols on liquid surfaces in motion such as rivers. Unlike wet deposition which is conditioned by washout and rainout (rain and clouds), dry deposition is a phenomenon that depends entirely on the characteristics of aerosols, receiving surfaces, and air flow. In practice, the evaluation of dry deposition is based on the estimation of flux modeling as the product of particle concentration and deposition velocity which can vary over several orders of magnitude depending on the receiving surfaces (forest, snow, urban, grassland...). This topic is motivated by the virtual non-existence of studies on the mechanisms of dry deposition on continental water systems such as rivers; and respect for submicron aerosols. They have the lowest deposition efficiencies and filtration and the longer residence time in the atmosphere. In addition, they are potentially the most dangerous to living beings because they can penetrate deeper into the airway. Due to the lack of data on the dry deposition of submicron aerosols on a liquid surface in motion, the approach was based on two axes: 1) the acquisition of experimental deposition velocities and 2) the analysis and interpretation of results through modeling. The experiments were performed with uranine aerosols released into the IOA wind tunnel (Interface Ocean Atmosphere) of the Institute for Research on Non Equilibrium Phenomena which is configured to study the coupling between the air flow and water. These experiments have given many dry deposition velocities for different configurations characterized according to wind

Dry deposition of submicron atmospheric aerosol over water surfaces in motion

International Nuclear Information System (INIS)

Calec, Nevenick

2013-01-01

Whether by chronic or accidental releases, the impact of a nuclear installation on the environment mainly depends on atmospheric transfers; and as the accidents at Chernobyl and Fukushima show, affect the contamination of surfaces and impacts in the medium and long-term on the environment and the population. In this context, this work focuses on the characterization and modeling of dry deposition of submicron aerosols on liquid surfaces in motion such as rivers. Unlike wet deposition which is conditioned by washout and rainout (rain and clouds), dry deposition is a phenomenon that depends entirely on the characteristics of aerosols, receiving surfaces, and air flow. In practice, the evaluation of dry deposition is based on the estimation of flux modeling as the product of particle concentration and deposition velocity which can vary over several orders of magnitude depending on the receiving surfaces (forest, snow, urban, grassland..). This topic is motivated by the virtual non-existence of studies on the mechanisms of dry deposition on continental water systems such as rivers; and respect for submicron aerosols. They have the lowest deposition efficiencies and filtration and the longer residence time in the atmosphere. In addition, they are potentially the most dangerous to living beings because they can penetrate deeper into the airway. Due to the lack of data on the dry deposition of submicron aerosols on a liquid surface in motion, the approach was based on two axes: 1) the acquisition of experimental deposition velocities and 2) the analysis and interpretation of results through modeling. The experiments were performed with uranine aerosols released into the IOA wind tunnel (Interface Ocean Atmosphere) of the Institute for Research on Non Equilibrium Phenomena which is configured to study the coupling between the air flow and water. These experiments have given many dry deposition velocities for different configurations characterized according to wind

Surface Flux Modeling for Air Quality Applications

Directory of Open Access Journals (Sweden)

Limei Ran

2011-08-01

Full Text Available For many gasses and aerosols, dry deposition is an important sink of atmospheric mass. Dry deposition fluxes are also important sources of pollutants to terrestrial and aquatic ecosystems. The surface fluxes of some gases, such as ammonia, mercury, and certain volatile organic compounds, can be upward into the air as well as downward to the surface and therefore should be modeled as bi-directional fluxes. Model parameterizations of dry deposition in air quality models have been represented by simple electrical resistance analogs for almost 30 years. Uncertainties in surface flux modeling in global to mesoscale models are being slowly reduced as more field measurements provide constraints on parameterizations. However, at the same time, more chemical species are being added to surface flux models as air quality models are expanded to include more complex chemistry and are being applied to a wider array of environmental issues. Since surface flux measurements of many of these chemicals are still lacking, resistances are usually parameterized using simple scaling by water or lipid solubility and reactivity. Advances in recent years have included bi-directional flux algorithms that require a shift from pre-computation of deposition velocities to fully integrated surface flux calculations within air quality models. Improved modeling of the stomatal component of chemical surface fluxes has resulted from improved evapotranspiration modeling in land surface models and closer integration between meteorology and air quality models. Satellite-derived land use characterization and vegetation products and indices are improving model representation of spatial and temporal variations in surface flux processes. This review describes the current state of chemical dry deposition modeling, recent progress in bi-directional flux modeling, synergistic model development research with field measurements, and coupling with meteorological land surface models.

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.

Methane flux to the atmosphere from the Deepwater Horizon oil disaster

Science.gov (United States)

Yvon-Lewis, Shari A.; Hu, Lei; Kessler, John

2011-01-01

The sea-to-air flux of methane from the blowout at the Deepwater Horizon was measured with substantial spatial and temporal resolution over the course of seven days in June 2010. Air and water concentrations were analyzed continuously from a flowing air line and a continuously flowing seawater equilibrator using cavity ring-down spectrometers (CRDS) and a gas chromatograph with a flame ionization detector (GC-FID). The results indicate a low flux of methane to the atmosphere (0.024 μmol m-2 d-1) with atmospheric and seawater equilibrium mixing ratios averaging 1.86 ppm and 2.85 ppm, respectively within the survey area. The oil leak, which was estimated to contain 30.2% methane by weight, was not a significant source of methane to the atmosphere during this study. Most of the methane emitted from the wellhead was dissolved in the deep ocean.

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

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.

PCDD/Fs atmospheric deposition fluxes and soil contamination close to a municipal solid waste incinerator.

Science.gov (United States)

Vassura, Ivano; Passarini, Fabrizio; Ferroni, Laura; Bernardi, Elena; Morselli, Luciano

2011-05-01

Bulk depositions and surface soil were collected in a suburban area, near the Adriatic Sea, in order to assess the contribution of a municipal solid waste incinerator to the area's total contamination with polychlorinated dibenzodioxins and polychlorinated dibenzofurans (PCDDs and PCDFs). Samples were collected at two sites, situated in the area most affected by plant emissions (according to the results of the Calpuff air dispersion model), and at an external site, considered as a reference. Results show that the studied area is subject to low contamination, as far as these compounds are concerned. Deposition fluxes range from 14.3 pg m(-2)d(-1) to 89.9 pg m(-2)d(-1) (0.75 pg-TEQ m(-2)d(-1) to 3.73 pg-TEQ m(-2)d(-1)) and no significant flow differences are observed among the three monitored sites. Total soil concentration amounts to 93.8 ng kg(-1) d.w. and 1.35 ng-TEQ kg(-1)d.w, on average, and confirms a strong homogeneity in the studied area. Furthermore, from 2006 to 2009, no PCDD/Fs enrichment in the soil was noticed. Comparing the relative congener distributions in environmental samples with those found in stack emissions from the incineration plant, significant differences are observed in the PCDD:PCDF ratio and in the contribution of the most chlorinated congeners. From this study we can conclude that the incineration plant is not the main source of PCDD/Fs in the studied area, which is apparently characterized by a homogeneous and widespread contamination situation, typical of an urban area. Copyright © 2011 Elsevier Ltd. All rights reserved.

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

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

Multi-year Estimates of Methane Fluxes in Alaska from an Atmospheric Inverse Model

Science.gov (United States)

Miller, S. M.; Commane, R.; Chang, R. Y. W.; Miller, C. E.; Michalak, A. M.; Dinardo, S. J.; Dlugokencky, E. J.; Hartery, S.; Karion, A.; Lindaas, J.; Sweeney, C.; Wofsy, S. C.

2015-12-01

We estimate methane fluxes across Alaska over a multi-year period using observations from a three-year aircraft campaign, the Carbon Arctic Reservoirs Vulnerability Experiment (CARVE). Existing estimates of methane from Alaska and other Arctic regions disagree in both magnitude and distribution, and before the CARVE campaign, atmospheric observations in the region were sparse. We combine these observations with an atmospheric particle trajectory model and a geostatistical inversion to estimate surface fluxes at the model grid scale. We first use this framework to estimate the spatial distribution of methane fluxes across the state. We find the largest fluxes in the south-east and North Slope regions of Alaska. This distribution is consistent with several estimates of wetland extent but contrasts with the distribution in most existing flux models. These flux models concentrate methane in warmer or more southerly regions of Alaska compared to the estimate presented here. This result suggests a discrepancy in how existing bottom-up models translate wetland area into methane fluxes across the state. We next use the inversion framework to explore inter-annual variability in regional-scale methane fluxes for 2012-2014. We examine the extent to which this variability correlates with weather or other environmental conditions. These results indicate the possible sensitivity of wetland fluxes to near-term variability in climate.

Study of Flux Ratio of C60 to Ar Cluster Ion for Hard DLC Film deposition

International Nuclear Information System (INIS)

Miyauchi, K.; Toyoda, N.; Kanda, K.; Matsui, S.; Kitagawa, T.; Yamada, I.

2003-01-01

To study the influence of the flux ratio of C60 molecule to Ar cluster ion on (diamond like carbon) DLC film characteristics, DLC films deposited under various flux ratios were characterized with Raman spectrometry and Near Edge X-ray Absorption Fine Structure (NEXAFS). From results of these measurements, hard DLC films were deposited when the flux ratio of C60 to Ar cluster ion was between 0.7 and 4. Furthermore the DLC film with constant sp2 content was obtained in the range of the ratio from 0.7 to 4, which contents are lower values than that of conventional films such as RF plasma. DLC films deposited under the ratio from 1 to 4 had hardness from 40 to 45GPa. It was shown that DLC films with stable properties of low sp2 content and high hardness were formed even when the fluxes were varied from 1 to 4 during deposition. It was indicated that this process was useful in the view of industrial application

Chemical characteristics, deposition fluxes and source apportionment of precipitation components in the Jiaozhou Bay, North China

Science.gov (United States)

Xing, Jianwei; Song, Jinming; Yuan, Huamao; Li, Xuegang; Li, Ning; Duan, Liqin; Qu, Baoxiao; Wang, Qidong; Kang, Xuming

2017-07-01

To systematically illustrate the chemical characteristics, deposition fluxes and potential sources of the major components in precipitation, 49 rainwater and snow water samples were collected in the Jiaozhou Bay from June 2015 to May 2016. We determined the pH, electric conductivity (EC) and the concentrations of main ions (Na+, K+, Ca2 +, Mg2 +, NH4+, SO42 -, NO3-, Cl- and F-) as well as analyzed their source contributions and atmospheric transport. The results showed that the precipitation samples were severely acidified with an annual volume-weighted mean (VWM) pH of 4.77. The frequency of acid precipitation (pH pollution level over the Jiaozhou Bay. Surprisingly, NH4+ (40.4%), which is higher than Ca2 + (29.3%), is the dominant species of cations, which is different from that in most areas of China. SO42 - was the most abundant anions, and accounted for 41.6% of the total anions. The wet deposition fluxes of sulfur (S) was 12.98 kg ha- 1 yr- 1. Rainfall, emission intensity and long-range transport of natural and anthropogenic pollutants together control the concentrations and wet deposition fluxes of chemical components in the precipitation. Non-sea-salt SO42 - and NO3- were the primary acid components while NH4+ and non-sea-salt Ca2 + were the dominating neutralizing constituents. The comparatively lower rainwater concentration of Ca2 + in the Jiaozhou Bay than that in other regions in Northern China likely to be a cause for the strong acidity of precipitation. Based on the combined enrichment factor and correlation analysis, the integrated contributions of sea-salt, crustal and anthropogenic sources to the total ions of precipitation were estimated to be 28.7%, 14.5% and 56.8%, respectively. However, the marine source fraction of SO42 - may be underestimated as the contribution from marine phytoplankton was neglected. Therefore, the precipitation components in the Jiaozhou Bay present complex chemical characteristics under the combined effects of natural

Noble Gas Surface Flux Simulations And Atmospheric Transport

Energy Technology Data Exchange (ETDEWEB)

Carrigan, Charles R. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Sun, Yunwei [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Simpson, Matthew D. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)

2017-09-30

Signatures from underground nuclear explosions or UNEs are strongly influenced by the containment regime surrounding them. The degree of gas leakage from the detonation cavity to the surface obviously affects the magnitude of surface fluxes of radioxenon that might be detected during the course of a Comprehensive Test Ban Treaty On-Site Inspection. In turn, the magnitude of surface fluxes will influence the downwind detectability of the radioxenon atmospheric signature from the event. Less obvious is the influence that leakage rates have on the evolution of radioxenon isotopes in the cavity or the downwind radioisotopic measurements that might be made. The objective of this letter report is to summarize our attempt to better understand how containment conditions affect both the detection and interpretation of radioxenon signatures obtained from sampling at the ground surface near an event as well as at greater distances in the atmosphere. In the discussion that follows, we make no attempt to consider other sources of radioactive noble gases such as natural backgrounds or atmospheric contamination and, for simplicity, only focus on detonation-produced radioxenon gases. Summarizing our simulations, they show that the decay of radioxenon isotopes (e.g., Xe-133, Xe-131m, Xe-133m and Xe-135) and their migration to the surface following a UNE means that the possibility of detecting these gases exists within a window of opportunity. In some cases, seeps or venting of detonation gases may allow significant quantities to reach the surface and be released into the atmosphere immediately following a UNE. In other release scenarios – the ones we consider here – hours to days may be required for gases to reach the surface at detectable levels. These release models are most likely more characteristic of “fully contained” events that lack prompt venting, but which still leak gas slowly across the surface for periods of months.

New Constraints on Terrestrial Surface-Atmosphere Fluxes of Gaseous Elemental Mercury Using a Global Database.

Science.gov (United States)

Agnan, Yannick; Le Dantec, Théo; Moore, Christopher W; Edwards, Grant C; Obrist, Daniel

2016-01-19

Despite 30 years of study, gaseous elemental mercury (Hg(0)) exchange magnitude and controls between terrestrial surfaces and the atmosphere still remain uncertain. We compiled data from 132 studies, including 1290 reported fluxes from more than 200,000 individual measurements, into a database to statistically examine flux magnitudes and controls. We found that fluxes were unevenly distributed, both spatially and temporally, with strong biases toward Hg-enriched sites, daytime and summertime measurements. Fluxes at Hg-enriched sites were positively correlated with substrate concentrations, but this was absent at background sites. Median fluxes over litter- and snow-covered soils were lower than over bare soils, and chamber measurements showed higher emission compared to micrometeorological measurements. Due to low spatial extent, estimated emissions from Hg-enriched areas (217 Mg·a(-1)) were lower than previous estimates. Globally, areas with enhanced atmospheric Hg(0) levels (particularly East Asia) showed an emerging importance of Hg(0) emissions accounting for half of the total global emissions estimated at 607 Mg·a(-1), although with a large uncertainty range (-513 to 1353 Mg·a(-1) [range of 37.5th and 62.5th percentiles]). The largest uncertainties in Hg(0) fluxes stem from forests (-513 to 1353 Mg·a(-1) [range of 37.5th and 62.5th percentiles]), largely driven by a shortage of whole-ecosystem fluxes and uncertain contributions of leaf-atmosphere exchanges, questioning to what degree ecosystems are net sinks or sources of atmospheric Hg(0).

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...

Atmospheric inversion of the surface CO2 flux with 13CO2 constraint

Science.gov (United States)

Chen, J. M.; Mo, G.; Deng, F.

2013-10-01

Observations of 13CO2 at 73 sites compiled in the GLOBALVIEW database are used for an additional constraint in a global atmospheric inversion of the surface CO2 flux using CO2 observations at 210 sites for the 2002-2004 period for 39 land regions and 11 ocean regions. This constraint is implemented using the 13CO2/CO2 flux ratio modeled with a terrestrial ecosystem model and an ocean model. These models simulate 13CO2 discrimination rates of terrestrial photosynthesis and respiration and ocean-atmosphere diffusion processes. In both models, the 13CO2 disequilibrium between fluxes to and from the atmosphere is considered due to the historical change in atmospheric 13CO2 concentration. For the 2002-2004 period, the 13CO2 constraint on the inversion increases the total land carbon sink from 3.40 to 3.70 Pg C yr-1 and decreases the total oceanic carbon sink from 1.48 to 1.12 Pg C yr-1. The largest changes occur in tropical areas: a considerable decrease in the carbon source in the Amazon forest, and this decrease is mostly compensated by increases in the ocean region immediately west of the Amazon and the southeast Asian land region. Our further investigation through different treatments of the 13CO2/CO2 flux ratio used in the inversion suggests that variable spatial distributions of the 13CO2 isotopic discrimination rate simulated by the models over land and ocean have considerable impacts on the spatial distribution of the inverted CO2 flux over land and the inversion results are not sensitive to errors in the estimated disequilibria over land and ocean.

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

Distribution, regional sources and deposition fluxes of organochlorine pesticides in precipitation in Guangzhou, South China

Science.gov (United States)

Huang, De-Yin; Peng, Ping'an; Xu, Yi-Gang; Sun, Cui-Xiang; Deng, Hong-Mei; Deng, Yun-Yun

2010-07-01

We analyzed rainwater collected from multiple sites, Guangzhou, China, from March to August 2005, with the aim to characterize the distribution, regional sources and deposition fluxes of organochlorine pesticides (OCPs) in South China. Eight species of organochlorine pesticide were detected, including hexachlorocyclohexanes (HCHs), dichlorodiphenyltrichloroethanes (DDTs), and endosulfans. Volume-weighted mean monthly total concentrations varied from 3.65 ± 0.95 to 9.37 ± 2.63 ng L - 1 , and the estimated total wet deposition flux was about 11.43 ± 3.27 µg m - 2 during the monitoring period. Pesticides were mainly detected in the dissolved phase. Distribution coefficients between particulate and dissolved phases in March and April were generally higher than in other months. HCHs, p,p'-DDD and p,p'-DDT in precipitation were attributed to both the residues and present usage of insecticides in Pearl River Delta. The concentrations of p,p'-DDD + p,p'-DDT were relatively high from April to August, which were related to the usage of antifouling paints containing DDT for fishing ships in seaports of the South China Sea in summer. In contrast, endosulfans were relatively high in March, which was related to their seasonal atmospheric transport from cotton fields in eastern China by the Asian winter monsoon. The consistency of the variation of endosulfans, p,p'-DDD and p,p'-DDT concentrations with the alternation of summer and winter monsoon suggested that the Asian monsoon played an important role in the long-range transport of OCPs. In addition, the wet deposition of OCPs may influence not only Pearl River water but also the surface land distributions of pesticides in the Guangzhou area, especially for endosulfans, p,p'-DDD and p,p'-DDT.

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.

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

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.

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

Methane Fluxes in West Siberia: 3-D Regional Model Simulation

International Nuclear Information System (INIS)

Jagovkina, S. V.; Karol, I. L.; Zubov, V. A.; Lagun, V. E.; Reshetnikov, A. I.; Rozanov, E. V.

2001-01-01

The West Siberian region is one of the main contributors of the atmospheric greenhouse gas methane due to the large areas of wetlands, rivers, lakes and numerous gas deposits situated there.But there are no reliable estimations of integral methane flux from this area into the atmosphere. For assessment of methane fluxes in West Siberia the specially constructed 3-D regional chemical transport model was applied. The 3-D distribution of methane is calculated on the basis of the current meteorological data fields(wind, temperature, geopotential) updated 4 times a day. The methane concentrations measured near the main gas fields of West Siberia in the summer season of 1999, were used for correction of methane flux intensity estimates obtained previously by comparison of measurements carried out in summer 1993 and 1996 with modelled methane mixing ratio distribution. This set of field and model experiments confirmed the preliminary conclusion about low leakage intensity: anthropogenic methane flux does not exceed 5-15% of total summer methane flux, estimated as 11-12 Mt CH 4 in summer from this region, in spite of the large areas of gas deposits located there

Observation of fluxes of electrons scattered by the atmosphere in the second Araks experiment

International Nuclear Information System (INIS)

Lyachov, S.B.; Managadze, G.G.

1980-01-01

This paper describes the results of the USHBA spectrometer measurements of the fluxes of atmospheric scattered electrons in the second Araks experiment. The experimental data are presented for heights from 100 to 140 km. The spectral distributions of the scattered electron fluxes are given and the altitude variation of their intensity is compared with the atmosphere models. The conclusion is made about the possible effect of rocket gassing on the electron scattering processes for definite angles of injection

Effects of elevated CO2 and nitrogen deposition on ecosystem carbon fluxes on the Sanjiang plain wetland in Northeast China.

Directory of Open Access Journals (Sweden)

Jianbo Wang

Full Text Available BACKGROUND: Increasing atmospheric CO2 and nitrogen (N deposition across the globe may affect ecosystem CO2 exchanges and ecosystem carbon cycles. Additionally, it remains unknown how increased N deposition and N addition will alter the effects of elevated CO2 on wetland ecosystem carbon fluxes. METHODOLOGY/PRINCIPAL FINDINGS: Beginning in 2010, a paired, nested manipulative experimental design was used in a temperate wetland of northeastern China. The primary factor was elevated CO2, accomplished using Open Top Chambers, and N supplied as NH4NO3 was the secondary factor. Gross primary productivity (GPP was higher than ecosystem respiration (ER, leading to net carbon uptake (measured by net ecosystem CO2 exchange, or NEE in all four treatments over the growing season. However, their magnitude had interannual variations, which coincided with air temperature in the early growing season, with the soil temperature and with the vegetation cover. Elevated CO2 significantly enhanced GPP and ER but overall reduced NEE because the stimulation caused by the elevated CO2 had a greater impact on ER than on GPP. The addition of N stimulated ecosystem C fluxes in both years and ameliorated the negative impact of elevated CO2 on NEE. CONCLUSION/SIGNIFICANCE: In this ecosystem, future elevated CO2 may favor carbon sequestration when coupled with increasing nitrogen deposition.

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

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,...

The interaction of the flux errors and transport errors in modeled atmospheric carbon dioxide concentrations

Science.gov (United States)

Feng, S.; Lauvaux, T.; Butler, M. P.; Keller, K.; Davis, K. J.; Jacobson, A. R.; Schuh, A. E.; Basu, S.; Liu, J.; Baker, D.; Crowell, S.; Zhou, Y.; Williams, C. A.

2017-12-01

Regional estimates of biogenic carbon fluxes over North America from top-down atmospheric inversions and terrestrial biogeochemical (or bottom-up) models remain inconsistent at annual and sub-annual time scales. While top-down estimates are impacted by limited atmospheric data, uncertain prior flux estimates and errors in the atmospheric transport models, bottom-up fluxes are affected by uncertain driver data, uncertain model parameters and missing mechanisms across ecosystems. This study quantifies both flux errors and transport errors, and their interaction in the CO2 atmospheric simulation. These errors are assessed by an ensemble approach. The WRF-Chem model is set up with 17 biospheric fluxes from the Multiscale Synthesis and Terrestrial Model Intercomparison Project, CarbonTracker-Near Real Time, and the Simple Biosphere model. The spread of the flux ensemble members represents the flux uncertainty in the modeled CO2 concentrations. For the transport errors, WRF-Chem is run using three physical model configurations with three stochastic perturbations to sample the errors from both the physical parameterizations of the model and the initial conditions. Additionally, the uncertainties from boundary conditions are assessed using four CO2 global inversion models which have assimilated tower and satellite CO2 observations. The error structures are assessed in time and space. The flux ensemble members overall overestimate CO2 concentrations. They also show larger temporal variability than the observations. These results suggest that the flux ensemble is overdispersive. In contrast, the transport ensemble is underdispersive. The averaged spatial distribution of modeled CO2 shows strong positive biogenic signal in the southern US and strong negative signals along the eastern coast of Canada. We hypothesize that the former is caused by the 3-hourly downscaling algorithm from which the nighttime respiration dominates the daytime modeled CO2 signals and that the latter

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

Iron fluxes to Talos Dome, Antarctica, over the past 200 kyr

Directory of Open Access Journals (Sweden)

P. Vallelonga

2013-03-01

Full Text Available Atmospheric fluxes of iron (Fe over the past 200 kyr are reported for the coastal Antarctic Talos Dome ice core, based on acid leachable Fe concentrations. Fluxes of Fe to Talos Dome were consistently greater than those at Dome C, with the greatest difference observed during interglacial climates. We observe different Fe flux trends at Dome C and Talos Dome during the deglaciation and early Holocene, attributed to a combination of deglacial activation of dust sources local to Talos Dome and the reorganisation of atmospheric transport pathways with the retreat of the Ross Sea ice shelf. This supports similar findings based on dust particle sizes and fluxes and Rare Earth Element fluxes. We show that Ca and Fe should not be used as quantitative proxies for mineral dust, as they all demonstrate different deglacial trends at Talos Dome and Dome C. Considering that a 20 ppmv decrease in atmospheric CO2 at the coldest part of the last glacial maximum occurs contemporaneously with the period of greatest Fe and dust flux to Antarctica, we confirm that the maximum contribution of aeolian dust deposition to Southern Ocean sequestration of atmospheric CO2 is approximately 20 ppmv.

Canopy uptake of atmospheric N deposition at a conifer forest: part I -canopy N budget, photosynthetic efficiency and net ecosystem exchange

International Nuclear Information System (INIS)

Sievering, H.; Tomaszewski, T.; Torizzo, J.

2007-01-01

Global carbon cycle assessments of anthropogenic nitrogen (N) deposition influences on carbon sequestration often assume enhanced sequestration results. This assumption was evaluated at a Rocky Mountains spruce-fir forest. Forest canopy N uptake (CNU) of atmospheric N deposition was estimated by combining event wet and throughfall N fluxes with gradient measured HNO 3 and NH 3 as well as inferred (NO x and particulate N) dry fluxes. Approximately 80% of the growing-season 3 kg N/ha total deposition is retained in canopy foliage and branches. This CNU constitutes ∼1/3 of canopy growing season new N supply at this conifer forest site. Daytime net ecosystem exchange (NEE) significantly (P = 0.006) and negatively (CO 2 uptake) correlated with CNU. Multiple regression indicates ∼20% of daytime NEE may be attributed to CNU (P < 0.02); more than soil water content. A wet deposition N-amendment study (Tomaszewski and Sievering), at canopy spruce branches, increased their growing-season CNU by 40-50% above ambient. Fluorometry and gas exchange results show N-amended spruce branches had greater photosynthetic efficiency and higher carboxylation rates than control and untreated branches. N-amended branches had 25% less photoinhibition, with a 5-9% greater proportion of foliar-N-in-Rubisco. The combined results provide, partly, a mechanistic explanation for the NEE dependence on CNU

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.

Toward an estimation of daily european CO2 fluxes at high spatial resolution by inversion of atmospheric transport

International Nuclear Information System (INIS)

Carouge, C.

2006-04-01

Since the end of the 1980's, measurements of atmospheric carbon dioxide have been used to estimate global and regional fluxes of CO 2 . This is possible because CO 2 concentration variation is directly linked to flux variation by atmospheric transport. We can find the spatial and temporal distribution of fluxes from concentration measurements by 'inverting' the atmospheric transport. Until recently, most CO 2 inversions have used monthly mean CO 2 atmospheric concentration measurements to infer monthly fluxes. Considering the sparseness of the global CO 2 measurement network, fluxes were a priori aggregated on sub-continental regions and distributed on a fixed spatial pattern within these regions. Only one flux coefficient per month for each region was optimized. With this strong constraint, estimated fluxes can be biased by non-perfect distribution of fluxes within each region (aggregation error). Therefore, flux estimation at model resolution is being developed where the hard constraint of a fixed distribution within a region is replaced by a soft constraint of covariances between flux uncertainties. The use of continuous observations from an increasing number of measurement sites offers a new challenge for inverse modelers. We investigate the use of daily averaged observations to infer daily CO 2 fluxes at model resolution over Europe. We have developed a global synthesis Bayesian inversion to invert daily fluxes at model resolution (50 x 50 km over Europe) from daily averaged CO 2 concentrations. We have obtained estimated fluxes for the year 2001 over Europe using the 10 European continuous sites from the AEROCARB network. The global atmospheric model LMDZt is used with a nested grid over Europe. It is necessary to add a priori spatial and temporal correlations between flux errors to constrain the Bayesian inversion. We present the impact on estimated fluxes of three different spatial correlations based on distance between pixels, climate and vegetation

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 Abundance of Atmospheric CO{sub 2} in Ocean Exoplanets: a Novel CO{sub 2} Deposition Mechanism

Energy Technology Data Exchange (ETDEWEB)

Levi, A.; Sasselov, D. [Harvard-Smithsonian Center for Astrophysics, 60 Garden Street, Cambridge, MA 02138 (United States); Podolak, M., E-mail: amitlevi.planetphys@gmail.com [Dept. of Geosciences, Tel Aviv University, Tel Aviv, 69978 (Israel)

2017-03-20

We consider super-Earth sized planets which have a water mass fraction large enough to form an external mantle composed of high-pressure water-ice polymorphs and also lack a substantial H/He atmosphere. We consider such planets in their habitable zone, so that their outermost condensed mantle is a global, deep, liquid ocean. For these ocean planets, we investigate potential internal reservoirs of CO{sub 2}, the amount of CO{sub 2} dissolved in the ocean for the various saturation conditions encountered, and the ocean-atmosphere exchange flux of CO{sub 2}. We find that, in a steady state, the abundance of CO{sub 2} in the atmosphere has two possible states. When wind-driven circulation is the dominant CO{sub 2} exchange mechanism, an atmosphere of tens of bars of CO{sub 2} results, where the exact value depends on the subtropical ocean surface temperature and the deep ocean temperature. When sea-ice formation, acting on these planets as a CO{sub 2} deposition mechanism, is the dominant exchange mechanism, an atmosphere of a few bars of CO{sub 2} is established. The exact value depends on the subpolar surface temperature. Our results suggest the possibility of a negative feedback mechanism, unique to water planets, where a reduction in the subpolar temperature drives more CO{sub 2} into the atmosphere to increase the greenhouse effect.

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

Surface-air mercury fluxes across Western North America: A synthesis of spatial trends and controlling variables

Energy Technology Data Exchange (ETDEWEB)

Eckley, Chris S., E-mail: eckley.chris@epa.gov [US Environmental Protection Agency, Region-10, Seattle, WA 98101 (United States); Tate, Mike T. [US Geological Survey, Middleton, WI 53562 (United States); Lin, Che-Jen [Center for Advances on Water and Air quality, Lamar University, Beaumont, TX 77710 (United States); Gustin, Mae [Department of Natural Resources & Environmental Science, University of Nevada, Reno, NV 89557 (United States); Dent, Stephen [CDM Smith, Portland, OR 97205 (United States); Eagles-Smith, Collin [US Geological Survey, Corvallis, OR 97331 (United States); Lutz, Michelle A. [US Geological Survey, Middleton, WI 53562 (United States); Wickland, Kimberly P. [US Geological Survey Boulder, CO 80303 (United States); Wang, Bronwen [US Geological Survey, Anchorage, AK 99508 (United States); Gray, John E. [US Geological Survey, Denver, CO 80225 (United States); Edwards, Grant C. [Department of Environment and Geography, Macquarie University, North Ryde, NSW 2109 (Australia); Krabbenhoft, Dave P. [US Geological Survey, Middleton, WI 53562 (United States); Smith, David B. [US Geological Survey, Denver, CO 80225 (United States)

2016-10-15

Mercury (Hg) emission and deposition can occur to and from soils, and are an important component of the global atmospheric Hg budget. This paper focuses on synthesizing existing surface-air Hg flux data collected throughout the Western North American region and is part of a series of geographically focused Hg synthesis projects. A database of existing Hg flux data collected using the dynamic flux chamber (DFC) approach from almost a thousand locations was created for the Western North America region. Statistical analysis was performed on the data to identify the important variables controlling Hg fluxes and to allow spatiotemporal scaling. The results indicated that most of the variability in soil-air Hg fluxes could be explained by variations in soil-Hg concentrations, solar radiation, and soil moisture. This analysis also identified that variations in DFC methodological approaches were detectable among the field studies, with the chamber material and sampling flushing flow rate influencing the magnitude of calculated emissions. The spatiotemporal scaling of soil-air Hg fluxes identified that the largest emissions occurred from irrigated agricultural landscapes in California. Vegetation was shown to have a large impact on surface-air Hg fluxes due to both a reduction in solar radiation reaching the soil as well as from direct uptake of Hg in foliage. Despite high soil Hg emissions from some forested and other heavily vegetated regions, the net ecosystem flux (soil flux + vegetation uptake) was low. Conversely, sparsely vegetated regions showed larger net ecosystem emissions, which were similar in magnitude to atmospheric Hg deposition (except for the Mediterranean California region where soil emissions were higher). The net ecosystem flux results highlight the important role of landscape characteristics in effecting the balance between Hg sequestration and (re-)emission to the atmosphere. - Highlights: • Soil-air Hg fluxes are an important component of the

Surface-air mercury fluxes across Western North America: A synthesis of spatial trends and controlling variables

International Nuclear Information System (INIS)

Eckley, Chris S.; Tate, Mike T.; Lin, Che-Jen; Gustin, Mae; Dent, Stephen; Eagles-Smith, Collin; Lutz, Michelle A.; Wickland, Kimberly P.; Wang, Bronwen; Gray, John E.; Edwards, Grant C.; Krabbenhoft, Dave P.; Smith, David B.

2016-01-01

Mercury (Hg) emission and deposition can occur to and from soils, and are an important component of the global atmospheric Hg budget. This paper focuses on synthesizing existing surface-air Hg flux data collected throughout the Western North American region and is part of a series of geographically focused Hg synthesis projects. A database of existing Hg flux data collected using the dynamic flux chamber (DFC) approach from almost a thousand locations was created for the Western North America region. Statistical analysis was performed on the data to identify the important variables controlling Hg fluxes and to allow spatiotemporal scaling. The results indicated that most of the variability in soil-air Hg fluxes could be explained by variations in soil-Hg concentrations, solar radiation, and soil moisture. This analysis also identified that variations in DFC methodological approaches were detectable among the field studies, with the chamber material and sampling flushing flow rate influencing the magnitude of calculated emissions. The spatiotemporal scaling of soil-air Hg fluxes identified that the largest emissions occurred from irrigated agricultural landscapes in California. Vegetation was shown to have a large impact on surface-air Hg fluxes due to both a reduction in solar radiation reaching the soil as well as from direct uptake of Hg in foliage. Despite high soil Hg emissions from some forested and other heavily vegetated regions, the net ecosystem flux (soil flux + vegetation uptake) was low. Conversely, sparsely vegetated regions showed larger net ecosystem emissions, which were similar in magnitude to atmospheric Hg deposition (except for the Mediterranean California region where soil emissions were higher). The net ecosystem flux results highlight the important role of landscape characteristics in effecting the balance between Hg sequestration and (re-)emission to the atmosphere. - Highlights: • Soil-air Hg fluxes are an important component of the

Atmospheric fall-out of metals around the Murano glass-making district (Venice, Italy).

Science.gov (United States)

Rossini, Paolo; Matteucci, Gabriele; Guerzoni, Stefano

2010-01-01

Murano's glass-makers have held a monopoly on quality glass-making for centuries known all over the world. Artistic glass manufacture entails exposure to complex mixtures of pollutants, including metals. A few studies have reported high levels of trace elements in marine waters, sediments and mussels around Murano and shown that emissions from Murano glass-making workshops significantly influence air quality in the Venice area. Nevertheless, to date, there is very little information on atmospheric concentrations and virtually none on atmospheric deposition fluxes of trace elements around the island. This study presents data on the distribution of trace elements in the air and atmospheric depositions around Murano, based on a 2-year sampling period. Airborne PM10 particulate matter was collected daily in the period December 2001-June 2003 (254 air samples), and atmospheric depositions were collected every 19 +/- 6 days, in the period August 2001-July 2003 (38 samples) on the roof of the Experimental Glass Laboratory on the island of Murano. All samples were analysed by ICP-MS for As, Cd, Cr, Cu, Fe, Mn, Ni, Pb, Sb, Se and Zn contents. Atmospheric concentrations of As, Cd, Cr, Ni, Pb, Se and Zn were 1-2 orders of magnitude greater on the island of Murano than in the nearest urban areas (Venice and Mestre), with values higher than those reported for European industrial sites. The atmospheric deposition fluxes of all elements were also higher in Murano than those detected by other studies in Venice and Mestre and in the Porto Marghera industrial zone, with As, Cd, Sb and Se 1-2 orders of magnitude higher. In order to study the spatial variability of the atmospheric fall-out, data from other sampling stations belonging to Venice atmospheric deposition monitoring networks were used. A decreasing gradient from Murano to the closer leeward stations was observed for As, Cd and Se. Pb and Zn deposition fluxes in Venice were also comparable to those observed in the Porto

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).

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.

Comparison of energy fluxes at the land surface-atmosphere interface in an Alpine valley as simulated with different models

Directory of Open Access Journals (Sweden)

G. Grossi

2003-01-01

Full Text Available Within the framework of a research project coupling meteorological and hydrological models in mountainous areas a distributed Snow-Soil-Vegetation-Atmosphere Transfer model was developed and applied to simulate the energy fluxes at the land surface – atmosphere interface in an Alpine valley (Toce Valley - North Italy during selected flood events in the last decade. Energy fluxes simulated by the distributed energy transfer model were compared with those simulated by a limited area meteorological model for the event of June 1997 and the differences in the spatial and temporal distribution. The Snow/Soil-Vegetation-Atmosphere Transfer model was also applied to simulate the energy fluxes at the land surface-atmosphere interface for a single cell, assumed to be representative of the Siberia site (Toce Valley, where a micro-meteorological station was installed and operated for 2.5 months in autumn 1999. The Siberia site is very close to the Nosere site, where a standard meteorological station was measuring precipitation, air temperature and humidity, global and net radiation and wind speed during the same special observing period. Data recorded by the standard meteorological station were used to force the energy transfer model and simulate the point energy fluxes at the Siberia site, while turbulent fluxes observed at the Siberia site were used to derive the latent heat flux from the energy balance equation. Finally, the hourly evapotranspiration flux computed by this procedure was compared to the evapotranspiration flux simulated by the energy transfer model. Keywords: energy exchange processes, land surface-atmosphere interactions, turbulent fluxes

Effect of inclusions on microstructure and toughness of deposited metals of self-shielded flux cored wires

International Nuclear Information System (INIS)

Zhang, Tianli; Li, Zhuoxin; Kou, Sindo; Jing, Hongyang; Li, Guodong; Li, Hong; Jin Kim, Hee

2015-01-01

The effect of inclusions on the microstructure and toughness of the deposited metals of self-shielded flux cored wires was investigated by optical microscopy, electron microscopy and mechanical testing. The deposited metals of three different wires showed different levels of low temperature impact toughness at −40 °C mainly because of differences in the properties of inclusions. The inclusions formed in the deposited metals as a result of deoxidation caused by the addition of extra Al–Mg alloy and ferromanganese to the flux. The inclusions, spherical in shape, were mixtures of Al 2 O 3 and MgO. Inclusions predominantly Al 2 O 3 and 0.3–0.8 μm in diameter were effective for nucleation of acicular ferrite. However, inclusions predominantly MgO were promoted by increasing Mg in the flux and were more effective than Al 2 O 3 inclusions of the same size. These findings suggest that the control of inclusions can be an effective way to improve the impact toughness of the deposited metal

The Chemistry of Atmosphere-Forest Exchange (CAFE Model – Part 2: Application to BEARPEX-2007 observations

Directory of Open Access Journals (Sweden)

G. M. Wolfe

2011-02-01

Full Text Available In a companion paper, we introduced the Chemistry of Atmosphere-Forest Exchange (CAFE model, a vertically-resolved 1-D chemical transport model designed to probe the details of near-surface reactive gas exchange. Here, we apply CAFE to noontime observations from the 2007 Biosphere Effects on Aerosols and Photochemistry Experiment (BEARPEX-2007. In this work we evaluate the CAFE modeling approach, demonstrate the significance of in-canopy chemistry for forest-atmosphere exchange and identify key shortcomings in the current understanding of intra-canopy processes.

CAFE generally reproduces BEARPEX-2007 observations but requires an enhanced radical recycling mechanism to overcome a factor of 6 underestimate of hydroxyl (OH concentrations observed during a warm (~29 °C period. Modeled fluxes of acyl peroxy nitrates (APN are quite sensitive to gradients in chemical production and loss, demonstrating that chemistry may perturb forest-atmosphere exchange even when the chemical timescale is long relative to the canopy mixing timescale. The model underestimates peroxy acetyl nitrate (PAN fluxes by 50% and the exchange velocity by nearly a factor of three under warmer conditions, suggesting that near-surface APN sinks are underestimated relative to the sources. Nitric acid typically dominates gross dry N deposition at this site, though other reactive nitrogen (NO_y species can comprise up to 28% of the N deposition budget under cooler conditions. Upward NO₂ fluxes cause the net above-canopy NO_y flux to be ~30% lower than the gross depositional flux. CAFE under-predicts ozone fluxes and exchange velocities by ~20%. Large uncertainty in the parameterization of cuticular and ground deposition precludes conclusive attribution of non-stomatal fluxes to chemistry or surface uptake. Model-measurement comparisons of vertical concentration gradients for several emitted species suggests that the lower canopy airspace may be

Deposition of nitrogen into the North Sea

DEFF Research Database (Denmark)

Leeuw, G. de; Skjøth, C.A.; Hertel, O.

2003-01-01

The flux of nitrogen species from the atmosphere into the ocean, with emphasis on coastal waters, was addressed during the ANICE project (Atmospheric Nitrogen Inputs into the Coastal Ecosystem). ANICE focused on quantifying the deposition of atmospheric inputs of inorganic nitrogen compounds (HNO3...... and Harwich/Newcastle. These measurements provided data for sensitivity studies of a variety of problems associated with the coastal region that are not easily evaluated with larger scale models, to constrain models and to test model results. Concentrations of nitrogen compounds over the North Sea...... on experimental results and small-scale model studies. In particular, effects of the aerosol size distribution on the nitrogen deposition are discussed. (C) 2003 Elsevier Ltd. All rights reserved....

Nitrogen distribution and cycling through water flows in a subtropical bamboo forest under high level of atmospheric deposition.

Science.gov (United States)

Tu, Li-hua; Hu, Ting-xing; Zhang, Jian; Huang, Li-hua; Xiao, Yin-long; Chen, Gang; Hu, Hong-ling; Liu, Li; Zheng, Jiang-kun; Xu, Zhen-Feng; Chen, Liang-hua

2013-01-01

The hydrological cycle is an important way of transportation and reallocation of reactive nitrogen (N) in forest ecosystems. However, under a high level of atmospheric N deposition, the N distribution and cycling through water flows in forest ecosystems especially in bamboo ecosystems are not well understood. In order to investigate N fluxes through water flows in a Pleioblastus amarus bamboo forest, event rainfall/snowfall (precipitation, PP), throughfall (TF), stemflow (SF), surface runoff (SR), forest floor leachate (FFL), soil water at the depth of 40 cm (SW1) and 100 cm (SW2) were collected and measured through the whole year of 2009. Nitrogen distribution in different pools in this ecosystem was also measured. Mean N pools in vegetation and soil (0-1 m) were 351.7 and 7752.8 kg ha(-1). Open field nitrogen deposition at the study site was 113.8 kg N ha(-1) yr(-1), which was one of the highest in the world. N-NH4(+), N-NO3(-) and dissolved organic N (DON) accounted for 54%, 22% and 24% of total wet N deposition. Net canopy accumulated of N occurred with N-NO3(-) and DON but not N-NH4(+). The flux of total dissolved N (TDN) to the forest floor was greater than that in open field precipitation by 17.7 kg N ha(-1) yr(-1), due to capture of dry and cloudwater deposition net of canopy uptake. There were significant negative exponential relationships between monthly water flow depths and monthly mean TDN concentrations in PP, TF, SR, FFL and SW1. The open field nitrogen deposition through precipitation is very high over the world, which is the main way of reactive N input in this bamboo ecosystem. The water exchange and N consume mainly occurred in the litter floor layer and topsoil layer, where most of fine roots of bamboo distributed.

Wet and Dry Atmospheric Depositions of Inorganic Nitrogen during Plant Growing Season in the Coastal Zone of Yellow River Delta

Directory of Open Access Journals (Sweden)

Junbao Yu

2014-01-01

Full Text Available The ecological problems caused by dry and wet deposition of atmospheric nitrogen have been widespread concern in the world. In this study, wet and dry atmospheric depositions were monitored in plant growing season in the coastal zone of the Yellow River Delta (YRD using automatic sampling equipment. The results showed that SO42- and Na+ were the predominant anion and cation, respectively, in both wet and dry atmospheric depositions. The total atmospheric nitrogen deposition was ~2264.24 mg m−2, in which dry atmospheric nitrogen deposition was about 32.02%. The highest values of dry and wet atmospheric nitrogen deposition appeared in May and August, respectively. In the studied area, NO3-–N was the main nitrogen form in dry deposition, while the predominant nitrogen in wet atmospheric deposition was NH4+–N with ~56.51% of total wet atmospheric nitrogen deposition. The average monthly attribution rate of atmospheric deposition of NO3-–N and NH4+–N was ~31.38% and ~20.50% for the contents of NO3-–N and NH4+–N in 0–10 cm soil layer, respectively, suggested that the atmospheric nitrogen was one of main sources for soil nitrogen in coastal zone of the YRD.

Wet and dry atmospheric depositions of inorganic nitrogen during plant growing season in the coastal zone of Yellow River Delta.

Science.gov (United States)

Yu, Junbao; Ning, Kai; Li, Yunzhao; Du, Siyao; Han, Guangxuan; Xing, Qinghui; Wu, Huifeng; Wang, Guangmei; Gao, Yongjun

2014-01-01

The ecological problems caused by dry and wet deposition of atmospheric nitrogen have been widespread concern in the world. In this study, wet and dry atmospheric depositions were monitored in plant growing season in the coastal zone of the Yellow River Delta (YRD) using automatic sampling equipment. The results showed that SO4 (2-) and Na(+) were the predominant anion and cation, respectively, in both wet and dry atmospheric depositions. The total atmospheric nitrogen deposition was ~2264.24 mg m(-2), in which dry atmospheric nitrogen deposition was about 32.02%. The highest values of dry and wet atmospheric nitrogen deposition appeared in May and August, respectively. In the studied area, NO3 (-)-N was the main nitrogen form in dry deposition, while the predominant nitrogen in wet atmospheric deposition was NH4 (+)-N with ~56.51% of total wet atmospheric nitrogen deposition. The average monthly attribution rate of atmospheric deposition of NO3 (-)-N and NH4 (+)-N was ~31.38% and ~20.50% for the contents of NO3 (-)-N and NH4 (+)-N in 0-10 cm soil layer, respectively, suggested that the atmospheric nitrogen was one of main sources for soil nitrogen in coastal zone of the YRD.

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)

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...

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

Verification of land-atmosphere coupling in forecast models, reanalyses and land surface models using flux site observations.

Science.gov (United States)

Dirmeyer, Paul A; Chen, Liang; Wu, Jiexia; Shin, Chul-Su; Huang, Bohua; Cash, Benjamin A; Bosilovich, Michael G; Mahanama, Sarith; Koster, Randal D; Santanello, Joseph A; Ek, Michael B; Balsamo, Gianpaolo; Dutra, Emanuel; Lawrence, D M

2018-02-01

We confront four model systems in three configurations (LSM, LSM+GCM, and reanalysis) with global flux tower observations to validate states, surface fluxes, and coupling indices between land and atmosphere. Models clearly under-represent the feedback of surface fluxes on boundary layer properties (the atmospheric leg of land-atmosphere coupling), and may over-represent the connection between soil moisture and surface fluxes (the terrestrial leg). Models generally under-represent spatial and temporal variability relative to observations, which is at least partially an artifact of the differences in spatial scale between model grid boxes and flux tower footprints. All models bias high in near-surface humidity and downward shortwave radiation, struggle to represent precipitation accurately, and show serious problems in reproducing surface albedos. These errors create challenges for models to partition surface energy properly and errors are traceable through the surface energy and water cycles. The spatial distribution of the amplitude and phase of annual cycles (first harmonic) are generally well reproduced, but the biases in means tend to reflect in these amplitudes. Interannual variability is also a challenge for models to reproduce. Our analysis illuminates targets for coupled land-atmosphere model development, as well as the value of long-term globally-distributed observational monitoring.

Increasing atmospheric deposition nitrogen and ammonium reduced microbial activity and changed the bacterial community composition of red paddy soil.

Science.gov (United States)

Zhou, Fengwu; Cui, Jian; Zhou, Jing; Yang, John; Li, Yong; Leng, Qiangmei; Wang, Yangqing; He, Dongyi; Song, Liyan; Gao, Min; Zeng, Jun; Chan, Andy

2018-03-27

Atmospheric deposition nitrogen (ADN) increases the N content in soil and subsequently impacts microbial activity of soil. However, the effects of ADN on paddy soil microbial activity have not been well characterized. In this study, we studied how red paddy soil microbial activity responses to different contents of ADN through a 10-months ADN simulation on well managed pot experiments. Results showed that all tested contents of ADN fluxes (27, 55, and 82kgNha -1 when its ratio of NH 4 + /NO 3 - -N (R N ) was 2:1) enhanced the soil enzyme activity and microbial biomass carbon and nitrogen and 27kgNha -1 ADN had maximum effects while comparing with the fertilizer treatment. Generally, increasing of both ADN flux and R N (1:2, 1:1 and 2:1 with the ADN flux of 55kgNha -1 ) had similar reduced effects on microbial activity. Furthermore, both ADN flux and R N significantly reduced soil bacterial alpha diversity (pADN flux and R N were the main drivers in shaping paddy soil bacteria community. Overall, the results have indicated that increasing ADN flux and ammonium reduced soil microbial activity and changed the soil bacterial community. The finding highlights how paddy soil microbial community response to ADN and provides information for N management in paddy soil. Copyright © 2018 Elsevier B.V. All rights reserved.

Atmospheric Mercury Deposition to a Remote Islet in the Subtropical Northwest Pacific Ocean

Science.gov (United States)

Sheu, G.; Lin, N.

2013-12-01

Thirty-four weekly rainwater samples were collected in 2009 at Pengjiayu, a remote islet in the subtropical Northwest (NW) Pacific Ocean with an area of 1.14 km^2, to study the distribution of rainwater mercury (Hg) concentrations and associated wet deposition fluxes. This is the first study concerning wet Hg deposition to the subtropical NW Pacific Ocean downwind of the East Asian continent, which is the major source region for Hg emissions worldwide. Sample Hg concentrations ranged from 2.25 to 22.33 ng L^-1, with a volume-weighted mean (VWM) concentration of 8.85 ng L^-1. The annual wet Hg deposition flux was 10.18 μg m^-2, about 2.5 times the fluxes measured at sites on the Pacific coast of the USA, supporting the hypothesis that deposition is higher in the western than in the eastern Pacific. Seasonal VWM concentrations were 7.23, 11.58, 7.82, and 9.84 ng L^-1, whereas seasonal wet deposition fluxes were 2.14, 3.45, 2.38, and 2.21 μg m^-2, for spring, summer, fall and winter, respectively. Higher summer wet Hg deposition was a function of both higher rainwater Hg concentration and greater rainfall. The seasonal pattern of rainwater Hg concentrations was the opposite of the general seasonal pattern of the East Asian air pollutant export. Since there is no significant anthropogenic Hg emission source on the islet of Pengjiayu, the observed high summertime rainwater Hg concentration hints at the importance of Hg(0) oxidation and/or scavenging of upper-altitude reactive gaseous Hg (RGM) by deep convection. Direct anthropogenic RGM emissions from the East Asian continent may not contribute significantly to the rainwater Hg concentrations, but anthropogenic Hg(0) emissions could be transported to the upper troposphere or marine boundary layer where they can be oxidized to produce RGM, which will then be effectively scavenged by cloud water and rainwater.

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)

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

Science.gov (United States)

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.

Wet and Dry Atmospheric Mercury Deposition Accumulates in Watersheds of the Northeastern United States

Science.gov (United States)

Boyer, E. W.; Grant, C.; Grimm, J.; Drohan, P. J.; Bennett, J.; Lawler, D.

2013-12-01

Mercury emissions to the atmosphere from coal-fired power plants and other sources such as waste incineration can be deposited to landscapes in precipitation and in dry fallout. Some mercury reaches watersheds and streams, where it can accumulate in sediments and biota. Human exposure to mercury occurs primarily through fish consumption, and currently mercury fish eating advisories are in place for many of the streams and lakes in the state. Here, we explored mercury in air, soils, water, and biota. To quantify atmospheric mercury deposition, we measured both wet and dry mercury deposition at over 10 locations in Pennsylvania, from which we present variation in mercury deposition and initial assessments of factors affecting the patterns. Further, we simulated mercury deposition at unmonitored locations in Pennsylvania and the northeastern United States over space and time with a high-resolution modeling technique that reflects storm tracks and air flow patterns. To consider mercury accumulation in watersheds, we collected data on soil mercury concentrations in a set of soil samples, and collected baseline data on mercury in streams draining 35 forested watersheds across Pennsylvania, spanning gradients of atmospheric deposition, climate and geology. Mercury concentrations were measured in stream water under base-flow conditions, in streambed sediments, aquatic mosses, and in fish tissues from brook trout. Results indicate that wet and dry atmospheric deposition is a primary source of mercury that is accumulating in watersheds of Pennsylvania and the northeastern United States.

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

Atmospheric concentrations and deposition of oxidised sulfur and nitrogen species at Petaling Jaya, Malaysia, 1993-1998

Energy Technology Data Exchange (ETDEWEB)

Ayers, G.P.; Gillett, R.W.; Manins, P.C. [CSIRO Atmospheric Research, Aspendale, VIC (Australia); Peng Leong Chow; Fook Lim Sze [Malaysian Meteorological Service, Petaling Jaya (Malaysia); Kong Cheah Wai [Tenaga Nasional R and D Berhad, Kajang (Malaysia)

2000-02-01

Wet-only rainwater composition, acid-precursor gas mixing ratios and aerosol loading were determined from weekly-averaged samples at Petaling Jaya, Malaysia, over the five year period from March 1993 to March 1998. Annual deposition fluxes of acidic sulfur and nitrogen species estimated from these data show this site to be heavily impacted by acidic deposition, with total oxidised sulfur plus nitrogen deposition in the range 277-480 meq m{sup -2} yr{sup -1}. Average contributions were 56% as sulfur species, 44% as nitrogen species, with wet deposition in this region of high rainfall accounting for 67% of total deposition. Thus total acid deposition fluxes were equivalent to levels that provided motivation for emissions reduction programs in both Europe and North America. The possibility of adverse environmental effects in Malaysia caused by acid deposition therefore merits serious consideration and assessment.

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.

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

Observation-based modelling of permafrost carbon fluxes with accounting for deep carbon deposits and thermokarst activity

Science.gov (United States)

Schneider von Deimling, T.; Grosse, G.; Strauss, J.; Schirrmeister, L.; Morgenstern, A.; Schaphoff, S.; Meinshausen, M.; Boike, J.

2015-06-01

High-latitude soils store vast amounts of perennially frozen and therefore inert organic matter. With rising global temperatures and consequent permafrost degradation, a part of this carbon stock will become available for microbial decay and eventual release to the atmosphere. We have developed a simplified, two-dimensional multi-pool model to estimate the strength and timing of future carbon dioxide (CO2) and methane (CH4) fluxes from newly thawed permafrost carbon (i.e. carbon thawed when temperatures rise above pre-industrial levels). We have especially simulated carbon release from deep deposits in Yedoma regions by describing abrupt thaw under newly formed thermokarst lakes. The computational efficiency of our model allowed us to run large, multi-centennial ensembles under various scenarios of future warming to express uncertainty inherent to simulations of the permafrost carbon feedback. Under moderate warming of the representative concentration pathway (RCP) 2.6 scenario, cumulated CO2 fluxes from newly thawed permafrost carbon amount to 20 to 58 petagrams of carbon (Pg-C) (68% range) by the year 2100 and reach 40 to 98 Pg-C in 2300. The much larger permafrost degradation under strong warming (RCP8.5) results in cumulated CO2 release of 42 to 141 Pg-C and 157 to 313 Pg-C (68% ranges) in the years 2100 and 2300, respectively. Our estimates only consider fluxes from newly thawed permafrost, not from soils already part of the seasonally thawed active layer under pre-industrial climate. Our simulated CH4 fluxes contribute a few percent to total permafrost carbon release yet they can cause up to 40% of total permafrost-affected radiative forcing in the 21st century (upper 68% range). We infer largest CH4 emission rates of about 50 Tg-CH4 per year around the middle of the 21st century when simulated thermokarst lake extent is at its maximum and when abrupt thaw under thermokarst lakes is taken into account. CH4 release from newly thawed carbon in wetland

Observation-based modelling of permafrost carbon fluxes with accounting for deep carbon deposits and thermokarst activity

Directory of Open Access Journals (Sweden)

T. Schneider von Deimling

2015-06-01

Full Text Available High-latitude soils store vast amounts of perennially frozen and therefore inert organic matter. With rising global temperatures and consequent permafrost degradation, a part of this carbon stock will become available for microbial decay and eventual release to the atmosphere. We have developed a simplified, two-dimensional multi-pool model to estimate the strength and timing of future carbon dioxide (CO2 and methane (CH4 fluxes from newly thawed permafrost carbon (i.e. carbon thawed when temperatures rise above pre-industrial levels. We have especially simulated carbon release from deep deposits in Yedoma regions by describing abrupt thaw under newly formed thermokarst lakes. The computational efficiency of our model allowed us to run large, multi-centennial ensembles under various scenarios of future warming to express uncertainty inherent to simulations of the permafrost carbon feedback. Under moderate warming of the representative concentration pathway (RCP 2.6 scenario, cumulated CO2 fluxes from newly thawed permafrost carbon amount to 20 to 58 petagrams of carbon (Pg-C (68% range by the year 2100 and reach 40 to 98 Pg-C in 2300. The much larger permafrost degradation under strong warming (RCP8.5 results in cumulated CO2 release of 42 to 141 Pg-C and 157 to 313 Pg-C (68% ranges in the years 2100 and 2300, respectively. Our estimates only consider fluxes from newly thawed permafrost, not from soils already part of the seasonally thawed active layer under pre-industrial climate. Our simulated CH4 fluxes contribute a few percent to total permafrost carbon release yet they can cause up to 40% of total permafrost-affected radiative forcing in the 21st century (upper 68% range. We infer largest CH4 emission rates of about 50 Tg-CH4 per year around the middle of the 21st century when simulated thermokarst lake extent is at its maximum and when abrupt thaw under thermokarst lakes is taken into account. CH4 release from newly thawed carbon in

Wire-mesh capped deposition sensors: Novel passive tool for coarse fraction flux estimation of radon thoron progeny in indoor environments

International Nuclear Information System (INIS)

Mayya, Y.S.; Mishra, Rosaline; Prajith, Rama; Sapra, B.K.; Kushwaha, H.S.

2010-01-01

Deposition-based 222 Rn and 220 Rn progeny sensors act as unique, passive tools for determining the long time-averaged progeny deposition fluxes in the environment. The use of these deposition sensors as progeny concentration monitors was demonstrated in typical indoor environments as conceptually superior alternatives to gas-based indirect monitoring methods. In the present work, the dependency of these deposition monitors on various environmental parameters is minimized by capping the deposition sensor with a suitable wire mesh. These wire-mesh capped deposition sensors measure the coarse fraction deposition flux, which is less dependent on the change in environmental parameters like ventilation rate and turbulence. The calibration of these wire-mesh capped coarse fraction progeny sensors was carried out by laboratory controlled experiments. These sensors were deployed both in indoor and in occupational environments having widely different ventilation rates. The obtained coarse fraction deposition velocities were fairly constant in these environments, which further confirmed that the signal on the wire-mesh capped sensors show the least dependency on the change in environmental parameters. This technique has the potential to serve as a passive particle sizer in the general context of nanoparticles using progeny species as surrogates. On the whole, there exists a strong case for developing a passive system that responds only to coarse fraction for providing alternative tools for dosimetry and environmental fine particle research. - Research highlights: → Wire-mesh capped deposition sensor measures the coarse fraction deposition flux → Coarse fraction deposition flux less dependent on environmental conditions → Wire-mesh capped deposition sensor as passive particle sizer

Prompt neutrino fluxes in the atmosphere with PROSA parton distribution functions

International Nuclear Information System (INIS)

Garzelli, M.V.; Moch, S.; Placakyte, R.; Sigl, G.; Cooper-Sarkar, A.

2016-11-01

Effects on atmospheric prompt neutrino fluxes of present uncertainties affecting the nucleon composition are studied by using the PROSA fit to parton distribution functions (PDFs). The PROSA fit extends the precision of the PDFs to low x, which is the kinematic region of relevance for high-energy neutrino production, by taking into account LHCb data on charm and bottom hadroproduction. In the range of neutrino energies explored by present Very Large Volume Neutrino Telescopes, it is found that PDF uncertainties are far smaller with respect to those due to renormalization and factorization scale variation and to assumptions on the cosmic ray composition, which at present dominate and limit our knowledge of prompt neutrino fluxes. A discussion is presented on how these uncertainties affect the expected number of atmospheric prompt neutrino events in the analysis of high-energy events characterized by interaction vertices fully contained within the instrumented volume of the detector, performed by the IceCube collaboration.

Nitrogen deposition in precipitation to a monsoon-affected eutrophic embayment: Fluxes, sources, and processes

Science.gov (United States)

Wu, Yunchao; Zhang, Jingping; Liu, Songlin; Jiang, Zhijian; Arbi, Iman; Huang, Xiaoping; Macreadie, Peter Ian

2018-06-01

Daya Bay in the South China Sea (SCS) has experienced rapid nitrogen pollution and intensified eutrophication in the past decade due to economic development. Here, we estimated the deposition fluxes of nitrogenous species, clarified the contribution of nitrogen from precipitation and measured ions and isotopic composition (δ15N and δ18O) of nitrate in precipitation in one year period to trace its sources and formation processes among different seasons. We found that the deposition fluxes of total dissolved nitrogen (TDN), NO3-, NH4+, NO2-, and dissolved organic nitrogen (DON) to Daya Bay were 132.5, 64.4 17.5, 1.0, 49.6 mmol m-2•yr-1, respectively. DON was a significant contributor to nitrogen deposition (37% of TDN), and NO3- accounted for 78% of the DIN in precipitation. The nitrogen deposition fluxes were higher in spring and summer, and lower in winter. Nitrogen from precipitation contributed nearly 38% of the total input of nitrogen (point sources input and dry and wet deposition) in Daya Bay. The δ15N-NO3- abundance, ion compositions, and air mass backward trajectories implicated that coal combustion, vehicle exhausts, and dust from mainland China delivered by northeast monsoon were the main sources in winter, while fossil fuel combustion (coal combustion and vehicle exhausts) and dust from PRD and southeast Asia transported by southwest monsoon were the main sources in spring; marine sources, vehicle exhausts and lightning could be the potential sources in summer. δ18O results showed that OH pathway was dominant in the chemical formation process of nitrate in summer, while N2O5+ DMS/HC pathways in winter and spring.

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.

Methane Flux to the Atmosphere from the Deepwater Horizon Oil Leak

Science.gov (United States)

Yvon-Lewis, S. A.; Hu, L.; Kessler, J. D.; Garcia Tigreros, F.; Chan, E. W.; Du, M.

2010-12-01

The unfortunate blowout at the BP Deepwater Horizon (DWH) oil rig on April 20, which killed 11 people, was releasing oil and methane at an average rate of 58,000 barrels per day into the deep ocean, until it was recently capped resulting in a total of 4.9 million barrels released (National Incident Command Report, 2010). The methane component of the emission was estimated at 40-60%. As part of a NSF funded RAPID award, the sea-to-air flux of methane from the blowout at the Deepwater Horizon was measured on board the R/V Cape Hatteras from June 11-20 with substantial spatial and temporal resolution over the course of seven days in June 2010. Air and water concentrations were analyzed continuously from a flowing air line and a continuously flowing seawater equilibrator using cavity ring-down spectrometers (CRDS) and a gas chromatograph with a flame ionization detector (GC-FID). The results indicate a low flux of methane to the atmosphere (0.024 μmol m^{-2} d^{-1}) with atmospheric and seawater equilibrium mixing ratios averaging 1.86 ppm and 2.85 ppm, respectively within the survey area. Most of the methane emitted from the wellhead was not emitted to the atmosphere. It dissolved into the water column at depth.

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

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.

The flux of ozone to a maize crop and the underlying soil during a growing season

NARCIS (Netherlands)

Pul, van W.A.J.

1992-01-01

To observe the flux or deposition of ozone above a maize crop, experiments were carried out during the growing season of maize in 1988. The flux of ozone was determined using meteorological techniques. The measurements used in the present study were carried out under atmospheric conditions

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

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

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.

Eddy covariance flux measurements of gaseous elemental mercury using cavity ring-down spectroscopy.

Science.gov (United States)

Pierce, Ashley M; Moore, Christopher W; Wohlfahrt, Georg; Hörtnagl, Lukas; Kljun, Natascha; Obrist, Daniel

2015-02-03

A newly developed pulsed cavity ring-down spectroscopy (CRDS) system for measuring atmospheric gaseous elemental mercury (GEM) concentrations at high temporal resolution (25 Hz) was used to successfully conduct the first eddy covariance (EC) flux measurements of GEM. GEM is the main gaseous atmospheric form, and quantification of bidirectional exchange between the Earth's surface and the atmosphere is important because gas exchange is important on a global scale. For example, surface GEM emissions from natural sources, legacy emissions, and re-emission of previously deposited anthropogenic pollution may exceed direct primary anthropogenic emissions. Using the EC technique for flux measurements requires subsecond measurements, which so far has not been feasible because of the slow time response of available instrumentation. The CRDS system measured GEM fluxes, which were compared to fluxes measured with the modified Bowen ratio (MBR) and a dynamic flux chamber (DFC). Measurements took place near Reno, NV, in September and October 2012 encompassing natural, low-mercury (Hg) background soils and Hg-enriched soils. During nine days of measurements with deployment of Hg-enriched soil in boxes within 60 m upwind of the EC tower, the covariance of GEM concentration and vertical wind speed was measured, showing that EC fluxes over an Hg-enriched area were detectable. During three separate days of flux measurements over background soils (without Hg-enriched soils), no covariance was detected, indicating fluxes below the detection limit. When fluxes were measurable, they strongly correlated with wind direction; the highest fluxes occurred when winds originated from the Hg-enriched area. Comparisons among the three methods showed good agreement in direction (e.g., emission or deposition) and magnitude, especially when measured fluxes originated within the Hg-enriched soil area. EC fluxes averaged 849 ng m(-2) h(-1), compared to DFC fluxes of 1105 ng m(-2) h(-1) and MBR fluxes

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

Remote Sensing and Sea-Truth Measurements of Methane Flux to the Atmosphere (HYFLUX project)

Energy Technology Data Exchange (ETDEWEB)

Ian MacDonald

2011-05-31

A multi-disciplinary investigation of distribution and magnitude of methane fluxes from seafloor gas hydrate deposits in the Gulf of Mexico was conducted based on results obtained from satellite synthetic aperture radar (SAR) remote sensing and from sampling conducted during a research expedition to three sites where gas hydrate occurs (MC118, GC600, and GC185). Samples of sediments, water, and air were collected from the ship and from an ROV submersible using sediments cores, niskin bottles attached to the ROV and to a rosette, and an automated sea-air interface collector. The SAR images were used to quantify the magnitude and distribution of natural oil and gas seeps that produced perennial oil slicks on the ocean surface. A total of 176 SAR images were processed using a texture classifying neural network algorithm, which segmented the ocean surface into oil-free and oil-covered water. Geostatistical analysis indicates that there are a total of 1081 seep formations distributed over the entire Gulf of Mexico basin. Oil-covered water comprised an average of 780.0 sq. km (sd 86.03) distributed with an area of 147,370 sq. km. Persistent oil and gas seeps were also detected with SAR sampling on other ocean margins located in the Black Sea, western coast of Africa, and offshore Pakistan. Analysis of sediment cores from all three sites show profiles of sulfate, sulfide, calcium and alkalinity that indicated anaerobic oxidation of methane with precipitation of authigenic carbonates. Difference among the three sampling sites may reflect the relative magnitude of methane flux. Methane concentrations in water column samples collected by ROV and rosette deployments from MC118 ranged from {approx}33,000 nM at the seafloor to {approx}12 nM in the mixed layer with isolated peaks up to {approx}13,670 nM coincident with the top of the gas hydrate stability field. Average plume methane, ethane, and propane concentrations in the mixed layer are 7, 630, and 9,540 times saturation

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

Does Silicate Weathering of Loess Affect Atmospheric CO2?

Science.gov (United States)

Anderson, S. P.

2002-12-01

Weathering of glacial loess may be a significant, yet unrecognized, component of the carbon cycle. Glaciers produce fine-grained sediment, exposing vast amounts of mineral surface area to weathering processes, yet silicate mineral weathering rates at glacier beds and of glacial till are not high. Thus, despite the tremendous potential for glaciers to influence global weathering rates and atmospheric CO2 levels, this effect has not been demonstrated. Loess, comprised of silt-clay sizes, may be the key glacial deposit in which silicate weathering rates are high. Loess is transported by wind off braid plains of rivers, and deposited broadly (order 100 km from the source) in vegetated areas. Both the fine grain size, and hence large mineral surface area, and presence of vegetation should render loess deposits highly susceptible to silicate weathering. These deposits effectively extend the geochemical impact of glaciation in time and space, and bring rock flour into conditions conducive to chemical weathering. A simple 1-d model of silicate weathering fluxes from a soil profile demonstrates the potential of loess deposition to enhance CO2 consumption. At each time step, computed mineral dissolution (using anorthite and field-based rate constants) modifies the size of mineral grains within the soil. In the case of a stable soil surface, this results in a gradual decline in weathering fluxes and CO2 consumption through time, as finer grain sizes dissolve away. Computed weathering fluxes for a typical loess, with an initial mean grain size of 25 μm, are an order of magnitude greater than fluxes from a non-loess soil that differs only in having a mean grain size of 320 μm. High weathering fluxes are maintained through time if loess is continually deposited. Deposition rates as low as 0.01 mm/yr (one loess grain thickness per year) can lead to a doubling of CO2 consumption rates within 5 ka. These results suggest that even modest loess deposition rates can significantly

The Influence of Air-Sea Fluxes on Atmospheric Aerosols During the Summer Monsoon Over the Tropical Indian Ocean

Science.gov (United States)

Zavarsky, Alex; Booge, Dennis; Fiehn, Alina; Krüger, Kirstin; Atlas, Elliot; Marandino, Christa

2018-01-01

During the summer monsoon, the western tropical Indian Ocean is predicted to be a hot spot for dimethylsulfide emissions, the major marine sulfur source to the atmosphere, and an important aerosol precursor. Other aerosol relevant fluxes, such as isoprene and sea spray, should also be enhanced, due to the steady strong winds during the monsoon. Marine air masses dominate the area during the summer monsoon, excluding the influence of continentally derived pollutants. During the SO234-2/235 cruise in the western tropical Indian Ocean from July to August 2014, directly measured eddy covariance DMS fluxes confirm that the area is a large source of sulfur to the atmosphere (cruise average 9.1 μmol m-2 d-1). The directly measured fluxes, as well as computed isoprene and sea spray fluxes, were combined with FLEXPART backward and forward trajectories to track the emissions in space and time. The fluxes show a significant positive correlation with aerosol data from the Terra and Suomi-NPP satellites, indicating a local influence of marine emissions on atmospheric aerosol numbers.

Atmospheric moisture transport and fresh water flux over oceans derived from spacebased sensors

Science.gov (United States)

Liu, W. T.; Tang, W.

2001-01-01

preliminary results will be shown to demonstrate the application of spacebased IMT and fresh water flux in ocean-atmosphere-land interaction studies, such as the hydrologica balance on Amazon rainfall and Indian monsoon.

Constraining Marsh Carbon Budgets Using Long-Term C Burial and Contemporary Atmospheric CO2 Fluxes

Science.gov (United States)

Forbrich, I.; Giblin, A. E.; Hopkinson, C. S.

2018-03-01

Salt marshes are sinks for atmospheric carbon dioxide that respond to environmental changes related to sea level rise and climate. Here we assess how climatic variations affect marsh-atmosphere exchange of carbon dioxide in the short term and compare it to long-term burial rates based on radiometric dating. The 5 years of atmospheric measurements show a strong interannual variation in atmospheric carbon exchange, varying from -104 to -233 g C m-2 a-1 with a mean of -179 ± 32 g C m-2 a-1. Variation in these annual sums was best explained by differences in rainfall early in the growing season. In the two years with below average rainfall in June, both net uptake and Normalized Difference Vegetation Index were less than in the other three years. Measurements in 2016 and 2017 suggest that the mechanism behind this variability may be rainfall decreasing soil salinity which has been shown to strongly control productivity. The net ecosystem carbon balance was determined as burial rate from four sediment cores using radiometric dating and was lower than the net uptake measured by eddy covariance (mean: 110 ± 13 g C m-2 a-1). The difference between these estimates was significant and may be because the atmospheric measurements do not capture lateral carbon fluxes due to tidal exchange. Overall, it was smaller than values reported in the literature for lateral fluxes and highlights the importance of investigating lateral C fluxes in future studies.

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.

Revised estimates of the annual net flux of carbon to the atmosphere from changes in land use and land management 1850-2000

International Nuclear Information System (INIS)

Houghton, R.A.

2003-01-01

Recent analyses of land-use change in the US and China, together with the latest estimates of tropical deforestation and afforestation from the FAO, were used to calculate a portion of the annual flux of carbon between terrestrial ecosystems and the atmosphere. The calculated flux includes only that portion of the flux resulting from direct human activity. In most regions, activities included the conversion of natural ecosystems to cultivated lands and pastures, including shifting cultivation, harvest of wood (for timber and fuel) and the establishment of tree plantations. In the US, woody encroachment and woodland thickening as a result of fire suppression were also included. The calculated flux of carbon does not include increases or decreases in carbon storage as a result of environmental changes (e.g.; increasing concentrations of CO 2 , N deposition, climatic change or pollution). Globally, the long-term (1850-2000) flux of carbon from changes in land use and management released 156 PgC to the atmosphere, about 60% of it from the tropics. Average annual fluxes during the 1980s and 1990s were 2.0 and 2.2 PgC/yr, respectively, dominated by releases of carbon from the tropics. Outside the tropics, the average net flux of carbon attributable to land-use change and management decreased from a source of 0.06 PgC/yr during the 1980s to a sink of 0.02 PgC/yr during the 1990s. According to the analyses summarized here, changes in land use were responsible for sinks in North America and Europe and for small sources in other non-tropical regions. The revisions were as large as 0.3 PgC/yr in individual regions but were largely offsetting, so that the global estimate for the 1980s was changed little from an earlier estimate. Uncertainties and recent improvements in the data used to calculate the flux of carbon from land-use change are reviewed, and the results are compared to other estimates of flux to evaluate the extent to which processes other than land-use change and

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

Differential flux measurement of atmospheric pion, muon, electron and positron energy spectra at balloon altitudes

Energy Technology Data Exchange (ETDEWEB)

Grimani, C.; Brunetti, M.T.; Codino, A. [Perugia Univ. (Italy)]|[INFN, Perugia (Italy); Papini, P.; Massimo Brancaccio, F.; Finetti, N. [Florence Univ. (Italy)]|[INFN, Florence (Italy); Stephens, S.A. [Tata Institute of Fundamental Researc, Bombay (International Commission on Radiation Units and Measurements); Basini, G.; Bongiorno, F. [INFN, Laboratori Nazionali di Frascati, Rome (Italy); Golden, R.L. [New Mexico State Univ. Las Cruces, NM (United States). Particle Astrophysics Lab.

1995-09-01

The fluxes of atmospheric electrons, positrons, positive and negative muons and negative pions have been determined using the NMSU Wizard-MASS2 balloons-borne instrument. The instrument was launched from Fort Sumner, New Mexico, (geomagnetic cut-off about 4.5 GV/c) on september 23, 1991. The flight lasted 9.8 hours and remained above 100.000 ft. Muons and negative pions were observed and their momenta were determined. Since these particles are not a part of the primary component, the measurement of their fluxes provides information regarding production and propagation of secondary particles in the atmosphere. Similarly, observations of electrons and positrons well below the geomagnetic cut-off provides insight into electromagnetic cascade processes in the upper atmosphere. In addition, the determination of the energy spectra of rare particles such as positrons can be used for background subtraction for cosmic ray experiments gathering data below a few g/cm{sup 2} of overlying atmosphere.

B33C-0612: Evaluation of Simulated Biospheric Carbon Dioxide Fluxes and Atmospheric Concentrations Using Global in Situ Observations

Science.gov (United States)

Philip, Sajeev; Johnson, Matthew S.; Potter, Christopher S.; Genovese, Vanessa

2016-01-01

Atmospheric mixing ratios of carbon dioxide (CO2) are largely controlled by anthropogenic emission sources and biospheric sources/sinks. Global biospheric fluxes of CO2 are controlled by complex processes facilitating the exchange of carbon between terrestrial ecosystems and the atmosphere. These processes which play a key role in these terrestrial ecosystem-atmosphere carbon exchanges are currently not fully understood, resulting in large uncertainties in the quantification of biospheric CO2 fluxes. Current models with these inherent deficiencies have difficulties simulating the global carbon cycle with high accuracy. We are developing a new modeling platform, GEOS-Chem-CASA by integrating the year-specific NASA-CASA (National Aeronautics and Space Administration - Carnegie Ames Stanford Approach) biosphere model with the GEOS-Chem (Goddard Earth Observation System-Chemistry) chemical transport model to improve the simulation of atmosphere-terrestrial ecosystem carbon exchange. We use NASA-CASA to explicitly represent the exchange of CO2 between terrestrial ecosystem and atmosphere by replacing the baseline GEOS-Chem land net CO2 flux and forest biomass burning CO2 emissions. We will present the estimation and evaluation of these "bottom-up" land CO2 fluxes, simulated atmospheric mixing ratios, and forest disturbance changes over the last decade. In addition, we will present our initial comparison of atmospheric column-mean dry air mole fraction of CO2 predicted by the model and those retrieved from NASA's OCO-2 (Orbiting Carbon Observatory-2) satellite instrument and model-predicted surface CO2 mixing ratios with global in situ observations. This evaluation is the first step necessary for our future work planned to constrain the estimates of biospheric carbon fluxes through "top-down" inverse modeling, which will improve our understanding of the processes controlling atmosphere-terrestrial ecosystem greenhouse gas exchanges, especially over regions which lack in

Liquid and chemical fluxes in precipitation, throughfall and stemflow

DEFF Research Database (Denmark)

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

2005-01-01

Wet deposition (WD), throughfall (TF) and stemflow (SF) measurements undertaken in a deciduous forest show 85% of the WD liquid flux is observed as TF and approximately 2% as SF. TF and SF were observed to be enriched in base cations and accordingly had an average pH of 6.1 and 5.9, respectively...... composition below sugar maples. The total atmospheric flux of inorganic nitrogen to the forest is approximately 14-18 kg-N ha(-1) yr(-1) supercript stop with approximately half taken up by the canopy. Associated experiments designed to quantify uncertainties in the nutrient fluxes included laboratory tests...

Atmospheric Forcing of the Winter Air–Sea Heat Fluxes over the Northern Red Sea

KAUST Repository

Papadopoulos, Vassilis P.; Abualnaja, Yasser; Josey, Simon A.; Bower, Amy; Raitsos, Dionysios E.; Kontoyiannis, Harilaos; Hoteit, Ibrahim

2013-01-01

The influence of the atmospheric circulation on the winter air–sea heat fluxes over the northern Red Sea is investigated during the period 1985–2011. The analysis based on daily heat flux values reveals that most of the net surface heat exchange variability depends on the behavior of the turbulent components of the surface flux (the sum of the latent and sensible heat). The large-scale composite sea level pressure (SLP) maps corresponding to turbulent flux minima and maxima show distinct atmospheric circulation patterns associated with each case. In general, extreme heat loss (with turbulent flux lower than −400 W m−2) over the northern Red Sea is observed when anticyclonic conditions prevail over an area extending from the Mediterranean Sea to eastern Asia along with a recession of the equatorial African lows system. Subcenters of high pressure associated with this pattern generate the required steep SLP gradient that enhances the wind magnitude and transfers cold and dry air masses from higher latitudes. Conversely, turbulent flux maxima (heat loss minimization with values from −100 to −50 W m−2) are associated with prevailing low pressures over the eastern Mediterranean and an extended equatorial African low that reaches the southern part of the Red Sea. In this case, a smooth SLP field over the northern Red Sea results in weak winds over the area that in turn reduce the surface heat loss. At the same time, southerlies blowing along the main axis of the Red Sea transfer warm and humid air northward, favoring heat flux maxima.

Atmospheric Forcing of the Winter Air–Sea Heat Fluxes over the Northern Red Sea

KAUST Repository

Papadopoulos, Vassilis P.

2013-03-01

The influence of the atmospheric circulation on the winter air–sea heat fluxes over the northern Red Sea is investigated during the period 1985–2011. The analysis based on daily heat flux values reveals that most of the net surface heat exchange variability depends on the behavior of the turbulent components of the surface flux (the sum of the latent and sensible heat). The large-scale composite sea level pressure (SLP) maps corresponding to turbulent flux minima and maxima show distinct atmospheric circulation patterns associated with each case. In general, extreme heat loss (with turbulent flux lower than −400 W m−2) over the northern Red Sea is observed when anticyclonic conditions prevail over an area extending from the Mediterranean Sea to eastern Asia along with a recession of the equatorial African lows system. Subcenters of high pressure associated with this pattern generate the required steep SLP gradient that enhances the wind magnitude and transfers cold and dry air masses from higher latitudes. Conversely, turbulent flux maxima (heat loss minimization with values from −100 to −50 W m−2) are associated with prevailing low pressures over the eastern Mediterranean and an extended equatorial African low that reaches the southern part of the Red Sea. In this case, a smooth SLP field over the northern Red Sea results in weak winds over the area that in turn reduce the surface heat loss. At the same time, southerlies blowing along the main axis of the Red Sea transfer warm and humid air northward, favoring heat flux maxima.

Nitrogen distribution and cycling through water flows in a subtropical bamboo forest under high level of atmospheric deposition.

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Li-hua Tu

Full Text Available BACKGROUND: The hydrological cycle is an important way of transportation and reallocation of reactive nitrogen (N in forest ecosystems. However, under a high level of atmospheric N deposition, the N distribution and cycling through water flows in forest ecosystems especially in bamboo ecosystems are not well understood. METHODOLOGY/PRINCIPAL FINDINGS: In order to investigate N fluxes through water flows in a Pleioblastus amarus bamboo forest, event rainfall/snowfall (precipitation, PP, throughfall (TF, stemflow (SF, surface runoff (SR, forest floor leachate (FFL, soil water at the depth of 40 cm (SW1 and 100 cm (SW2 were collected and measured through the whole year of 2009. Nitrogen distribution in different pools in this ecosystem was also measured. Mean N pools in vegetation and soil (0-1 m were 351.7 and 7752.8 kg ha(-1. Open field nitrogen deposition at the study site was 113.8 kg N ha(-1 yr(-1, which was one of the highest in the world. N-NH4(+, N-NO3(- and dissolved organic N (DON accounted for 54%, 22% and 24% of total wet N deposition. Net canopy accumulated of N occurred with N-NO3(- and DON but not N-NH4(+. The flux of total dissolved N (TDN to the forest floor was greater than that in open field precipitation by 17.7 kg N ha(-1 yr(-1, due to capture of dry and cloudwater deposition net of canopy uptake. There were significant negative exponential relationships between monthly water flow depths and monthly mean TDN concentrations in PP, TF, SR, FFL and SW1. CONCLUSIONS/SIGNIFICANCE: The open field nitrogen deposition through precipitation is very high over the world, which is the main way of reactive N input in this bamboo ecosystem. The water exchange and N consume mainly occurred in the litter floor layer and topsoil layer, where most of fine roots of bamboo distributed.

Impact of snow deposition on major and trace element concentrations and elementary fluxes in surface waters of the Western Siberian Lowland across a 1700 km latitudinal gradient

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Shevchenko, Vladimir P.; Pokrovsky, Oleg S.; Vorobyev, Sergey N.; Krickov, Ivan V.; Manasypov, Rinat M.; Politova, Nadezhda V.; Kopysov, Sergey G.; Dara, Olga M.; Auda, Yves; Shirokova, Liudmila S.; Kolesnichenko, Larisa G.; Zemtsov, Valery A.; Kirpotin, Sergey N.

2017-11-01

In order to better understand the chemical composition of snow and its impact on surface water hydrochemistry in the poorly studied Western Siberia Lowland (WSL), the surface layer of snow was sampled in February 2014 across a 1700 km latitudinal gradient (ca. 56.5 to 68° N). We aimed at assessing the latitudinal effect on both dissolved and particulate forms of elements in snow and quantifying the impact of atmospheric input to element storage and export fluxes in inland waters of the WSL. The concentration of dissolved+colloidal (metalloids (As, Sb), Mo and U in the discontinuous to continuous permafrost zone (64-68° N) can be explained solely by melting of accumulated snow. The impact of snow deposition on riverine fluxes of elements strongly increased northward, in discontinuous and continuous permafrost zones of frozen peat bogs. This was consistent with the decrease in the impact of rock lithology on river chemical composition in the permafrost zone of the WSL, relative to the permafrost-free regions. Therefore, the present study demonstrates significant and previously underestimated atmospheric input of many major and trace elements to their riverine fluxes during spring floods. A broader impact of this result is that current estimations of river water fluxes response to climate warming in high latitudes may be unwarranted without detailed analysis of winter precipitation.

Development and analysis of prognostic equations for mesoscale kinetic energy and mesoscale (subgrid scale) fluxes for large-scale atmospheric models

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Avissar, Roni; Chen, Fei

1993-01-01

Generated by landscape discontinuities (e.g., sea breezes) mesoscale circulation processes are not represented in large-scale atmospheric models (e.g., general circulation models), which have an inappropiate grid-scale resolution. With the assumption that atmospheric variables can be separated into large scale, mesoscale, and turbulent scale, a set of prognostic equations applicable in large-scale atmospheric models for momentum, temperature, moisture, and any other gaseous or aerosol material, which includes both mesoscale and turbulent fluxes is developed. Prognostic equations are also developed for these mesoscale fluxes, which indicate a closure problem and, therefore, require a parameterization. For this purpose, the mean mesoscale kinetic energy (MKE) per unit of mass is used, defined as E-tilde = 0.5 (the mean value of u'(sub i exp 2), where u'(sub i) represents the three Cartesian components of a mesoscale circulation (the angle bracket symbol is the grid-scale, horizontal averaging operator in the large-scale model, and a tilde indicates a corresponding large-scale mean value). A prognostic equation is developed for E-tilde, and an analysis of the different terms of this equation indicates that the mesoscale vertical heat flux, the mesoscale pressure correlation, and the interaction between turbulence and mesoscale perturbations are the major terms that affect the time tendency of E-tilde. A-state-of-the-art mesoscale atmospheric model is used to investigate the relationship between MKE, landscape discontinuities (as characterized by the spatial distribution of heat fluxes at the earth's surface), and mesoscale sensible and latent heat fluxes in the atmosphere. MKE is compared with turbulence kinetic energy to illustrate the importance of mesoscale processes as compared to turbulent processes. This analysis emphasizes the potential use of MKE to bridge between landscape discontinuities and mesoscale fluxes and, therefore, to parameterize mesoscale fluxes

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

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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.

Coastal upwelling fluxes of O2, N2O, and CO2 assessed from continuous atmospheric observations at Trinidad, California

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T. J. Lueker

2004-01-01

Full Text Available Continuous atmospheric records of O2/N2, CO2 and N2O obtained at Trinidad, California document the effects of air-sea exchange during coastal upwelling and plankton bloom events. The atmospheric records provide continuous observations of air-sea fluxes related to synoptic scale upwelling events over several upwelling seasons. Combined with satellite, buoy and local meteorology data, calculated anomalies in O2/N2 and N2O were utilized in a simple atmospheric transport model to compute air-sea fluxes during coastal upwelling. CO2 fluxes were linked to the oceanic component of the O2 fluxes through local hydrographic data and estimated as a function of upwelling intensity (surface ocean temperature and wind speed. Regional air-sea fluxes of O2/N2, N2O, and CO2 during coastal upwelling were estimated with the aid of satellite wind and SST data. Upwelling CO2 fluxes were found to represent ~10% of export production along the northwest coast of North America. Synoptic scale upwelling events impact the net exchange of atmospheric CO2 along the coastal margin, and will vary in response to the frequency and duration of alongshore winds that are subject to climate change.

Bioavailable atmospheric phosphorous supply to the global ocean: a 3-D global modeling study

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Myriokefalitakis, Stelios; Nenes, Athanasios; Baker, Alex R.; Mihalopoulos, Nikolaos; Kanakidou, Maria

2016-12-01

The atmospheric cycle of phosphorus (P) is parameterized here in a state-of-the-art global 3-D chemistry transport model, taking into account primary emissions of total P (TP) and soluble P (DP) associated with mineral dust, combustion particles from natural and anthropogenic sources, bioaerosols, sea spray and volcanic aerosols. For the present day, global TP emissions are calculated to be roughly 1.33 Tg-P yr-1, with the mineral sources contributing more than 80 % to these emissions. The P solubilization from mineral dust under acidic atmospheric conditions is also parameterized in the model and is calculated to contribute about one-third (0.14 Tg-P yr-1) of the global DP atmospheric source. To our knowledge, a unique aspect of our global study is the explicit modeling of the evolution of phosphorus speciation in the atmosphere. The simulated present-day global annual DP deposition flux is 0.45 Tg-P yr-1 (about 40 % over oceans), showing a strong spatial and temporal variability. Present-day simulations of atmospheric P aerosol concentrations and deposition fluxes are satisfactory compared with available observations, indicating however an underestimate of about 70 % on current knowledge of the sources that drive the P atmospheric cycle. Sensitivity simulations using preindustrial (year 1850) anthropogenic and biomass burning emission scenarios showed a present-day increase of 75 % in the P solubilization flux from mineral dust, i.e., the rate at which P is converted into soluble forms, compared to preindustrial times, due to increasing atmospheric acidity over the last 150 years. Future reductions in air pollutants due to the implementation of air-quality regulations are expected to decrease the P solubilization flux from mineral dust by about 30 % in the year 2100 compared to the present day. Considering, however, that all the P contained in bioaerosols is readily available for uptake by marine organisms, and also accounting for all other DP sources, a total

Comparison of mesoscale model and tower measurements of surface fluxes during Winter Icing and Storms Program/Atmospheric Radiation Measurement 91

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Oncley, S.P.; Dudhia, J.

1994-01-01

This study is an evaluation of the ability of the Pennsylvania State University/National Center for Atmospheric Research (NCAR) mesoscale model (MM4) to determine surface fluxes to see if measured fluxes should be assimilated into model runs. Fluxes were compared from a high-resolution (5 km grid spacing) MM4 run during one day of the Winter Icing and Storms Programs/Atmospheric Radiation Measurement (WISP/ARM) experiment (over NE Colorado in winter 1991) with direct flux measurements made from a tower over a representative site by a three-dimensional sonic anemometer and fast response temperature and humidity sensors. This tower was part of the NCAR Atmosphere-Surface Turbulent Exchange Research (ASTER) facility. Also, mean values were compared to check whether any differences were due to the model parameterization or model variables

An Inverse Modeling Approach to Investigate Past Lead Atmospheric Deposition in Southern Greenland

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Massa, C.; Monna, F.; Bichet, V.; Gauthier, E.; Richard, H.

2013-12-01

The aim of this study is to model atmospheric pollution lead fluxes using two different paleoenvironmental records, covering the last 2000 years, located in southern Greenland. Fifty five sediment samples from the Lake Igaliku sequence (61°00.403'N, 45°26.494'W) were analyzed for their Pb and Al contents, and for lead isotopic compositions. The second archive consists in a previously published dataset (Shotyk et al., 2003), including Zr and Pb concentrations, and lead isotopic compositions, obtained from a minerogenic peat deposit located 16 km northwest of Lake Igaliku (61°08.314'N, 45°33.703'W). As natural background concentrations are high and obliterate most of the airborne anthropogenic lead, it is not possible to isolate this anthropogenic contribution through time with classical methods (i.e. Pb is normalized to a lithogenic and conservative element). Moreover, the background 206Pb/207Pb ratio is rather noisy because of the wide geological heterogeneity of sediment sources, which further complicated unambiguous detection of the lead pollution. To overcome these difficulties, an inverse modeling approach based on assumptions about past lead inputs was applied. This method consists of simulating a range of anthropogenic fluxes to determine the best match between measured and simulated data, both for Pb concentrations and isotopic compositions. The model is validated by the coherence of the results obtained from the two independent datasets that must reflect a similar pollution history. Although notable 206Pb/207Pb ratio shifts suggest that the first signs of anthropogenic inputs may have occurred in the 15th century, the signal-to-noise ratio was too low to significantly influence the sediment composition. Nevertheless we were able to estimate that anthropogenic lead fluxes did not exceed 2700 μg m-2 yr-1, a maximum value recorded during the 1960s. The comparison with other records from the North Atlantic Islands reveals a spatial gradient most likely due

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

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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

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

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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.

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

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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.

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

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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.

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

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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.

Top-of-atmosphere radiative fluxes - Validation of ERBE scanner inversion algorithm using Nimbus-7 ERB data

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Suttles, John T.; Wielicki, Bruce A.; Vemury, Sastri

1992-01-01

The ERBE algorithm is applied to the Nimbus-7 earth radiation budget (ERB) scanner data for June 1979 to analyze the performance of an inversion method in deriving top-of-atmosphere albedos and longwave radiative fluxes. The performance is assessed by comparing ERBE algorithm results with appropriate results derived using the sorting-by-angular-bins (SAB) method, the ERB MATRIX algorithm, and the 'new-cloud ERB' (NCLE) algorithm. Comparisons are made for top-of-atmosphere albedos, longwave fluxes, viewing zenith-angle dependence of derived albedos and longwave fluxes, and cloud fractional coverage. Using the SAB method as a reference, the rms accuracy of monthly average ERBE-derived results are estimated to be 0.0165 (5.6 W/sq m) for albedos (shortwave fluxes) and 3.0 W/sq m for longwave fluxes. The ERBE-derived results were found to depend systematically on the viewing zenith angle, varying from near nadir to near the limb by about 10 percent for albedos and by 6-7 percent for longwave fluxes. Analyses indicated that the ERBE angular models are the most likely source of the systematic angular dependences. Comparison of the ERBE-derived cloud fractions, based on a maximum-likelihood estimation method, with results from the NCLE showed agreement within about 10 percent.

[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.

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

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

2012-08-01

Many alpine areas are experiencing deglaciation, biogeochemical changes driven by temperature rise, and changes in atmospheric deposition. There is mounting evidence that the water quality of alpine streams may be related to these changes, including rising atmospheric deposition of carbon (C) and nutrients. Given that barren alpine soils can be severely C limited, atmospheric deposition sources may be an important source of C and nutrients for these environments. We evaluated the magnitude of atmospheric deposition of C and nutrients to an alpine site, the Green Lake 4 catchment in the Colorado Rocky Mountains. Using a long-term dataset (2002-2010) of weekly atmospheric wet deposition and snowpack chemistry, we found that volume weighted mean dissolved organic carbon (DOC) concentrations were 1.12 ± 0.19 mg l-1, and weekly concentrations reached peaks as high at 6-10 mg l-1 every summer. Total dissolved nitrogen concentration also peaked in the summer, whereas total dissolved phosphorus and calcium concentrations were highest in the spring. To investigate potential sources of C in atmospheric deposition, we evaluated the chemical quality of dissolved organic matter (DOM) and relationships between DOM and other solutes in wet deposition. Relationships between DOC concentration, fluorescence, and nitrate and sulfate concentrations suggest that pollutants from nearby urban and agricultural sources and organic aerosols derived from sub-alpine vegetation may influence high summer DOC wet deposition concentrations. Interestingly, high DOC concentrations were also recorded during "dust-in-snow" events in the spring, which may reflect an association of DOM with dust. Detailed chemical and spectroscopic analyses conducted for samples collected in 2010 revealed that the DOM in many late spring and summer samples was less aromatic and polydisperse and of lower molecular weight than that of winter and fall samples. Our C budget estimates for the Green Lake 4 catchment

The Boston Methane Project: Mapping Surface Emissions to Inform Atmospheric Estimation of Urban Methane Flux

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Phillips, N.; Crosson, E.; Down, A.; Hutyra, L.; Jackson, R. B.; McKain, K.; Rella, C.; Raciti, S. M.; Wofsy, S. C.

2012-12-01

Lost and unaccounted natural gas can amount to over 6% of Massachusetts' total annual greenhouse gas inventory (expressed as equivalent CO2 tonnage). An unknown portion of this loss is due to natural gas leaks in pipeline distribution systems. The objective of the Boston Methane Project is to estimate the overall leak rate from natural gas systems in metropolitan Boston, and to compare this flux with fluxes from the other primary methane emissions sources. Companion talks at this meeting describe the atmospheric measurement and modeling framework, and chemical and isotopic tracers that can partition total atmospheric methane flux into natural gas and non-natural gas components. This talk focuses on estimation of surface emissions that inform the atmospheric modeling and partitioning. These surface emissions include over 3,300 pipeline natural gas leaks in Boston. For the state of Massachusetts as a whole, the amount of natural gas reported as lost and unaccounted for by utility companies was greater than estimated landfill emissions by an order of magnitude. Moreover, these landfill emissions were overwhelmingly located outside of metro Boston, while gas leaks are concentrated in exactly the opposite pattern, increasing from suburban Boston toward the urban core. Work is in progress to estimate spatial distribution of methane emissions from wetlands and sewer systems. We conclude with a description of how these spatial data sets will be combined and represented for application in atmospheric modeling.

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

Surface-Air Mercury Fluxes Across Western North America: A Synthesis of Spatial Trends and Controlling Variables.

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Eckley, C.; Tate, M.; Lin, C. J.; Gustin, M. S.; Dent, S.; Eagles-Smith, C.; Lutz, M.; Wickland, K.; Wang, B.; Gray, J.; Edwards, G. C.; Krabbenhoft, D. P.; Smith, D. B.

2016-12-01

Mercury (Hg) emission and deposition can occur to and from soils and are an important component of the global atmospheric Hg budget. This presentation focuses on synthesizing existing surface-air Hg flux data collected throughout the Western North American region and is part of a series of geographically focused Hg synthesis projects. A database of existing Hg flux data collected using the dynamic flux chamber (DFC) approach from almost a thousand locations was created for the Western North America region. Statistical analysis was performed on the data to identify the important variables controlling Hg fluxes and to allow spatiotemporal scaling. The results indicated that most of the variability in soil-air Hg fluxes could be explained by variations in soil-Hg concentrations, solar radiation, and soil moisture. This analysis also identified that variations in DFC methodological approaches were detectable among the field studies, with the chamber material and sampling flushing flow rate influencing the magnitude of calculated emissions. The spatiotemporal scaling of soil-air Hg fluxes identified that the largest emissions occurred from irrigated agricultural landscapes in California. Vegetation was shown to have a large impact on surface-air Hg fluxes due to both a reduction in solar radiation reaching the soil as well as from direct uptake of Hg in foliage. Despite high soil Hg emissions from some forested and other heavily vegetated regions, the net ecosystem flux (soil flux + vegetation uptake) was low. Conversely, sparsely vegetated regions showed larger net ecosystem emissions, which were similar in magnitude to atmospheric Hg deposition (except for the Mediterranean California region where soil emissions were higher). The net ecosystem flux results highlight the important role of landscape characteristics in effecting the balance between Hg sequestration and (re-)emission to the atmosphere.

Surface-air mercury fluxes across Western North America: A synthesis of spatial trends and controlling variables

Science.gov (United States)

Eckley, Chris S.; Tate, Michael T.; Lin, Che-Jen; Gustin, Mae S.; Dent, Stephen; Eagles-Smith, Collin A.; Lutz, Michelle A; Wickland, Kimberly; Wang, Bronwen; Gray, John E.; Edwards, Grant; Krabbenhoft, David P.; Smith, David

2016-01-01

Mercury (Hg) emission and deposition can occur to and from soils, and are an important component of the global atmospheric Hg budget. This paper focuses on synthesizing existing surface-air Hg flux data collected throughout the Western North American region and is part of a series of geographically focused Hg synthesis projects. A database of existing Hg flux data collected using the dynamic flux chamber (DFC) approach from almost a thousand locations was created for the Western North America region. Statistical analysis was performed on the data to identify the important variables controlling Hg fluxes and to allow spatiotemporal scaling. The results indicated that most of the variability in soil-air Hg fluxes could be explained by variations in soil-Hg concentrations, solar radiation, and soil moisture. This analysis also identified that variations in DFC methodological approaches were detectable among the field studies, with the chamber material and sampling flushing flow rate influencing the magnitude of calculated emissions. The spatiotemporal scaling of soil-air Hg fluxes identified that the largest emissions occurred from irrigated agricultural landscapes in California. Vegetation was shown to have a large impact on surface-air Hg fluxes due to both a reduction in solar radiation reaching the soil as well as from direct uptake of Hg in foliage. Despite high soil Hg emissions from some forested and other heavily vegetated regions, the net ecosystem flux (soil flux + vegetation uptake) was low. Conversely, sparsely vegetated regions showed larger net ecosystem emissions, which were similar in magnitude to atmospheric Hg deposition (except for the Mediterranean California region where soil emissions were higher). The net ecosystem flux results highlight the important role of landscape characteristics in effecting the balance between Hg sequestration and (re-)emission to the atmosphere.

SiB3 Modeled Global 1-degree Hourly Biosphere-Atmosphere Carbon Flux, 1998-2006

Data.gov (United States)

National Aeronautics and Space Administration — The Simple Biosphere Model, Version 3 (SiB3) was used to produce a global data set of hourly carbon fluxes between the atmosphere and the terrestrial biosphere for...

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)

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.

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

Sea ice-atmospheric interaction: Application of multispectral satellite data in polar surface energy flux estimates

Science.gov (United States)

Steffen, Konrad; Key, J.; Maslanik, J.; Schweiger, A.

1993-01-01

This is the third annual report on: Sea Ice-Atmosphere Interaction - Application of Multispectral Satellite Data in Polar Surface Energy Flux Estimates. The main emphasis during the past year was on: radiative flux estimates from satellite data; intercomparison of satellite and ground-based cloud amounts; radiative cloud forcing; calibration of the Advanced Very High Resolution Radiometer (AVHRR) visible channels and comparison of two satellite derived albedo data sets; and on flux modeling for leads. Major topics covered are arctic clouds and radiation; snow and ice albedo, and leads and modeling.

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.

Impact of air-sea drag coefficient for latent heat flux on large scale climate in coupled and atmosphere stand-alone simulations

Science.gov (United States)

Torres, Olivier; Braconnot, Pascale; Marti, Olivier; Gential, Luc

2018-05-01

The turbulent fluxes across the ocean/atmosphere interface represent one of the principal driving forces of the global atmospheric and oceanic circulation. Despite decades of effort and improvements, representation of these fluxes still presents a challenge due to the small-scale acting turbulent processes compared to the resolved scales of the models. Beyond this subgrid parameterization issue, a comprehensive understanding of the impact of air-sea interactions on the climate system is still lacking. In this paper we investigates the large-scale impacts of the transfer coefficient used to compute turbulent heat fluxes with the IPSL-CM4 climate model in which the surface bulk formula is modified. Analyzing both atmosphere and coupled ocean-atmosphere general circulation model (AGCM, OAGCM) simulations allows us to study the direct effect and the mechanisms of adjustment to this modification. We focus on the representation of latent heat flux in the tropics. We show that the heat transfer coefficients are highly similar for a given parameterization between AGCM and OAGCM simulations. Although the same areas are impacted in both kind of simulations, the differences in surface heat fluxes are substantial. A regional modification of heat transfer coefficient has more impact than uniform modification in AGCM simulations while in OAGCM simulations, the opposite is observed. By studying the global energetics and the atmospheric circulation response to the modification, we highlight the role of the ocean in dampening a large part of the disturbance. Modification of the heat exchange coefficient modifies the way the coupled system works due to the link between atmospheric circulation and SST, and the different feedbacks between ocean and atmosphere. The adjustment that takes place implies a balance of net incoming solar radiation that is the same in all simulations. As there is no change in model physics other than drag coefficient, we obtain similar latent heat flux

Low temperature magnetron sputter deposition of polycrystalline silicon thin films using high flux ion bombardment

International Nuclear Information System (INIS)

Gerbi, Jennifer E.; Abelson, John R.

2007-01-01

We demonstrate that the microstructure of polycrystalline silicon thin films depends strongly on the flux of low energy ions that bombard the growth surface during magnetron sputter deposition. The deposition system is equipped with external electromagnetic coils which, through the unbalanced magnetron effect, provide direct control of the ion flux independent of the ion energy. We report the influence of low energy ( + on the low temperature ( + ions to silicon neutrals (J + /J 0 ) during growth by an order of magnitude (from 3 to 30) enables the direct nucleation of polycrystalline Si on glass and SiO 2 coated Si at temperatures below 400 degree sign C. We discuss possible mechanisms for this enhancement of crystalline microstructure, including the roles of enhanced adatom mobility and the formation of shallow, mobile defects

Atmospheric nitrogen deposition in the Yangtze River basin: Spatial pattern and source attribution

International Nuclear Information System (INIS)

Xu, Wen; Zhao, Yuanhong; Liu, Xuejun; Dore, Anthony J.; Zhang, Lin; Liu, Lei; Cheng, Miaomiao

2018-01-01

The Yangtze River basin is one of the world's hotspots for nitrogen (N) deposition and likely plays an important role in China's riverine N output. Here we constructed a basin-scale total dissolved inorganic N (DIN) deposition (bulk plus dry) pattern based on published data at 100 observational sites between 2000 and 2014, and assessed the relative contributions of different reactive N (N r ) emission sectors to total DIN deposition using the GEOS-Chem model. Our results show a significant spatial variation in total DIN deposition across the Yangtze River basin (33.2 kg N ha −1 yr −1 on average), with the highest fluxes occurring mainly in the central basin (e.g., Sichuan, Hubei and Hunan provinces, and Chongqing municipality). This indicates that controlling N deposition should build on mitigation strategies according to local conditions, namely, implementation of stricter control of N r emissions in N deposition hotspots but moderate control in the areas with low N deposition levels. Total DIN deposition in approximately 82% of the basin area exceeded the critical load of N deposition for semi-natural ecosystems along the basin. On the basin scale, the dominant source of DIN deposition is fertilizer use (40%) relative to livestock (11%), industry (13%), power plant (9%), transportation (9%), and others (18%, which is the sum of contributions from human waste, residential activities, soil, lighting and biomass burning), suggesting that reducing NH 3 emissions from improper fertilizer (including chemical and organic fertilizer) application should be a priority in curbing N deposition. This, together with distinct spatial variations in emission sector contributions to total DIN deposition also suggest that, in addition to fertilizer, major emission sectors in different regions of the basin should be considered when developing synergistic control measures. - Highlights: • Total DIN deposition fluxes showed a significant spatial variation in the

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

Atmospheric Inputs of Nitrogen, Carbon, and Phosphorus across an Urban Area: Unaccounted Fluxes and Canopy Influences

Science.gov (United States)

Decina, Stephen M.; Templer, Pamela H.; Hutyra, Lucy R.

2018-02-01

Rates of atmospheric deposition are declining across the United States, yet urban areas remain hotspots of atmospheric deposition. While past studies show elevated rates of inorganic nitrogen (N) deposition in cities, less is known about atmospheric inputs of organic N, organic carbon (C), and organic and inorganic phosphorus (P), all of which can affect ecosystem processes, water quality, and air quality. Further, the effect of the tree canopy on amounts and forms of nutrients reaching urban ground surfaces is not well-characterized. We measured growing season rates of total N, organic C, and total P in bulk atmospheric inputs, throughfall, and soil solution around the greater Boston area. We found that organic N constitutes a third of total N inputs, organic C inputs are comparable to rural inputs, and inorganic P inputs are 1.2 times higher than those in sewage effluent. Atmospheric inputs are enhanced two-to-eight times in late spring and are elevated beneath tree canopies, suggesting that trees augment atmospheric inputs to ground surfaces. Additionally, throughfall inputs may directly enter runoff when trees extend above impervious surfaces, as is the case with 26.1% of Boston's tree canopy. Our results indicate that the urban atmosphere is a significant source of elemental inputs that may impact urban ecosystems and efforts to improve water quality, particularly in terms of P. Further, as cities create policies encouraging tree planting to provide ecosystem services, locating trees above permeable surfaces to reduce runoff nutrient loads may be essential to managing urban biogeochemical cycling and water quality.

A Long-term Forest Fertilization Experiment to Understand Ecosystem Responses to Atmospheric Nitrogen Deposition

Science.gov (United States)

Baron, J.; Advani, S. M.; Allen, J.; Boot, C.; Denef, K.; Denning, S.; Hall, E.; Moore, J. C.; Reuth, H.; Ryan, M. G.; Shaw, E.

2016-12-01

Long-term field experiments can reveal changes in ecosystem processes that may not be evident in short-term studies. Short-term measurements or experiments may have narrower objectives or unrealistic treatments in order to see a change, whereas long-term studies can reveal complex interactions that take longer to manifest. We report results from a long-term experiment (1996 to present) in subalpine forests to simulate the consequences of sustained atmospheric nitrogen (N) deposition. Loch Vale watershed in Rocky Mountain National Park, the location of the experiment, has received an order of magnitude greater atmospheric N deposition than estimated background since mid-20th Century. Augmenting that, in 1996 we began adding 25 kg NH4NO3 ha-1 yr-1 to three 30m x 30m old-growth Engelmann spruce and subalpine fir plots. Treated stands were matched by nearby controls. N addition caused rapid leaching of nitrate and cations from soils, and increased N mineralization and nitrification rates. These observations in the fertilized plots have been sustained over time. Soluble aluminum concentrations do not differ significantly between fertilized and control plots, but treated soils are now markedly more acidic (pH of 4.7) than original soil and controls (pH of 5.1); further acidification might increase aluminum leaching. Effects on soil carbon were complex, mediated by reductions in total microbial biomass, decreases in arbuscular mychorrizal and saprotropic fungi, and increased potential rates of N enzyme degrading activities. Initial soil C:N of 24 was lower than similar soils in low N deposition stands (C:N of 36). The C:N declined to 22 with treatment. Fertilized plots lost 11% soil C, but the mechanism is unclear. We did not measure changes in C inputs from litter, microbial biomass, or plant uptake, but there was no change in summer CO2 flux, measured in 2003, 2004, and 2014. Leaching of DOC from fertilized plots was elevated throughout the experiment, providing one

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)

Scaling in situ cosmogenic nuclide production rates using analytical approximations to atmospheric cosmic-ray fluxes

Science.gov (United States)

Lifton, Nathaniel; Sato, Tatsuhiko; Dunai, Tibor J.

2014-01-01

Several models have been proposed for scaling in situ cosmogenic nuclide production rates from the relatively few sites where they have been measured to other sites of interest. Two main types of models are recognized: (1) those based on data from nuclear disintegrations in photographic emulsions combined with various neutron detectors, and (2) those based largely on neutron monitor data. However, stubborn discrepancies between these model types have led to frequent confusion when calculating surface exposure ages from production rates derived from the models. To help resolve these discrepancies and identify the sources of potential biases in each model, we have developed a new scaling model based on analytical approximations to modeled fluxes of the main atmospheric cosmic-ray particles responsible for in situ cosmogenic nuclide production. Both the analytical formulations and the Monte Carlo model fluxes on which they are based agree well with measured atmospheric fluxes of neutrons, protons, and muons, indicating they can serve as a robust estimate of the atmospheric cosmic-ray flux based on first principles. We are also using updated records for quantifying temporal and spatial variability in geomagnetic and solar modulation effects on the fluxes. A key advantage of this new model (herein termed LSD) over previous Monte Carlo models of cosmogenic nuclide production is that it allows for faster estimation of scaling factors based on time-varying geomagnetic and solar inputs. Comparing scaling predictions derived from the LSD model with those of previously published models suggest potential sources of bias in the latter can be largely attributed to two factors: different energy responses of the secondary neutron detectors used in developing the models, and different geomagnetic parameterizations. Given that the LSD model generates flux spectra for each cosmic-ray particle of interest, it is also relatively straightforward to generate nuclide-specific scaling

Spatial variation in atmospheric nitrogen deposition on low canopy vegetation

International Nuclear Information System (INIS)

Verhagen, Rene; Diggelen, Rudy van

2006-01-01

Current knowledge about the spatial variation of atmospheric nitrogen deposition on a local scale is limited, especially for vegetation with a low canopy. We measured nitrogen deposition on artificial vegetation at variable distances of local nitrogen emitting sources in three nature reserves in the Netherlands, differing in the intensity of agricultural practices in the surroundings. In the nature reserve located in the most intensive agricultural region nitrogen deposition decreased with increasing distance to the local farms, until at a distance of 1500 m from the local nitrogen emitting sources the background level of 15 kg N ha -1 yr -1 was reached. No such trend was observed in the other two reserves. Interception was considerably lower than in woodlands and hence affected areas were larger. The results are discussed in relation to the prospects for the conservation or restoration of endangered vegetation types of nutrient-poor soil conditions. - Areas with low canopy vegetation are affected over much larger distances by nitrogen deposition than woodlands

Global observations and modeling of atmosphere-surface exchange of elemental mercury: a critical review

Science.gov (United States)

Zhu, Wei; Lin, Che-Jen; Wang, Xun; Sommar, Jonas; Fu, Xuewu; Feng, Xinbin

2016-04-01

Reliable quantification of air-surface fluxes of elemental Hg vapor (Hg0) is crucial for understanding mercury (Hg) global biogeochemical cycles. There have been extensive measurements and modeling efforts devoted to estimating the exchange fluxes between the atmosphere and various surfaces (e.g., soil, canopies, water, snow, etc.) in the past three decades. However, large uncertainties remain due to the complexity of Hg0 bidirectional exchange, limitations of flux quantification techniques and challenges in model parameterization. In this study, we provide a critical review on the state of science in the atmosphere-surface exchange of Hg0. Specifically, the advancement of flux quantification techniques, mechanisms in driving the air-surface Hg exchange and modeling efforts are presented. Due to the semi-volatile nature of Hg0 and redox transformation of Hg in environmental media, Hg deposition and evasion are influenced by multiple environmental variables including seasonality, vegetative coverage and its life cycle, temperature, light, moisture, atmospheric turbulence and the presence of reactants (e.g., O3, radicals, etc.). However, the effects of these processes on flux have not been fundamentally and quantitatively determined, which limits the accuracy of flux modeling. We compile an up-to-date global observational flux database and discuss the implication of flux data on the global Hg budget. Mean Hg0 fluxes obtained by micrometeorological measurements do not appear to be significantly greater than the fluxes measured by dynamic flux chamber methods over unpolluted surfaces (p = 0.16, one-tailed, Mann-Whitney U test). The spatiotemporal coverage of existing Hg0 flux measurements is highly heterogeneous with large data gaps existing in multiple continents (Africa, South Asia, Middle East, South America and Australia). The magnitude of the evasion flux is strongly enhanced by human activities, particularly at contaminated sites. Hg0 flux observations in East

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

Fog deposition fluxes of water and ions to a mountainous site in Central Europe

Science.gov (United States)

Klemm, Otto; Wrzesinsky, Thomas

2007-09-01

Fog and precipitation composition and deposition were measured over a 1-yr period. Ion concentrations were higher in fog than in precipitation by factors of between 6 and 18. The causes of these differences were less dilution of fog water due to non-availability of condensable water vapour, and more efficient transfer of surface emissions to fog water as compared to rain water or snow. Fogwater and dissolved ions depositions were measured with eddy covariance in combination with a bulk fogwater collector. Annual fogwater deposition was 9.4% that of precipitation. The annual deposition of ions through fog was of the same order as that for precipitation. Ammonium, representing local emission sources, had 46% more annual deposition through fog than through precipitation. The fog droplet number and mass size distributions are reported. Fog droplets of 15 μm diameter contribute most to the deposition flux. The variability of processes and parameters contributing to deposition of ions through fog (ion concentrations in fog water, liquid water content in air, fog duration and turbulence) is high.

The Effects of Atmospheric Nitrogen Deposition on Terrestrial and Freshwater Biodiversity

NARCIS (Netherlands)

Baron, J.S.; Barber, M.; Adams, M.; Dobben, van H.F.

2014-01-01

This chapter reports the findings of a Working Group on how atmospheric nitrogen (N) deposition affects both terrestrial and freshwater biodiversity. Regional and global scale impacts on biodiversity are addressed, together with potential indicators. Key conclusions are that: the rates of loss in

Comparative pick-up ion distributions at Mars and Venus: Consequences for atmospheric deposition and escape

Science.gov (United States)

Curry, Shannon M.; Luhmann, Janet; Ma, Yingjuan; Liemohn, Michael; Dong, Chuanfei; Hara, Takuya

2015-09-01

Without the shielding of a substantial intrinsic dipole magnetic field, the atmospheres of Mars and Venus are particularly susceptible to similar atmospheric ion energization and scavenging processes. However, each planet has different attributes and external conditions controlling its high altitude planetary ion spatial and energy distributions. This paper describes analogous test particle simulations in background MHD fields that allow us to compare the properties and fates, precipitation or escape, of the mainly O+ atmospheric pick-up ions at Mars and Venus. The goal is to illustrate how atmospheric and planetary scales affect the upper atmospheres and space environments of our terrestrial planet neighbors. The results show the expected convection electric field-related hemispheric asymmetries in both precipitation and escape, where the degree of asymmetry at each planet is determined by the planetary scale and local interplanetary field strength. At Venus, the kinetic treatment of O+ reveals a strong nightside source of precipitation while Mars' crustal fields complicate the simple asymmetry in ion precipitation and drive a dayside source of precipitation. The pickup O+ escape pattern at both Venus and Mars exhibits low energy tailward escape, but Mars exhibits a prominent, high energy 'polar plume' feature in the hemisphere of the upward convection electric field while the Venus ion wake shows only a modest poleward concentration. The overall escape is larger at Venus than Mars (2.1 ×1025 and 4.3 ×1024 at solar maximum, respectively), but the efficiency (likelihood) of O+ escaping is 2-3 times higher at Mars. The consequences of these comparisons for pickup ion related atmospheric energy deposition, loss rates, and detection on spacecraft including PVO, VEX, MEX and MAVEN are considered. In particular, both O+ precipitation and escape show electric field controlled asymmetries that grow with energy, while the O+ fluxes and energy spectra at selected spatial

Atmospheric Nitrogen Deposition and the Properties of Soils in Forests of Vologda Region

Science.gov (United States)

Kudrevatykh, I. Yu.; Ivashchenko, K. V.; Ananyeva, N. D.; Ivanishcheva, E. A.

2018-02-01

Twenty plots (20 m2 each) were selected in coniferous and mixed forests of the industrial Vologda district and the Vytegra district without developed industries in Vologda region. In March, snow cores corresponding to the snow cover depth were taken on these plots. In August, soil samples from the 0- to 20-cm layer of litter-free soddy-podzolic soil (Albic Retisol (Ochric)) were taken on the same plots in August. The content of mineral nitrogen (Nmin), including its ammonium (NH+ 4) and nitrate (NO- 3) forms, was determined in the snow (meltwater) and soil. The contents of total organic carbon, total nitrogen, and elements (Al, Ca); pH; particle size distribution; and microbiological parameters―carbon of microbial biomass (Cmic) and microbial respiration (MR)―were determined in the soil. The ratio MR/Cmic = qCO2 (specific respiration of microbial biomass, or soil microbial metabolic quotient) was calculated. The content of Nmic in meltwater of two districts was 1.7 mg/L on the average (1.5 and 0.3 mg/L for the NH+ 4 and NO- 3 forms, respectively). The annual atmospheric deposition was 0.6-8.9 kg Nmin/ha, the value of which in the Vologda district was higher than in the Vytegra district by 40%. Reliable correlations were found between atmospheric NH+ 4 depositions and Cmic (-0.45), between NH+ 4 and qCO2 (0.56), between atmospheric NO- 3 depositions and the soil NO- 3 (-0.45), and between NO- 3 and qCO2 (-0.58). The content of atmospheric Nmin depositions correlated with the ratios C/N (-0.46) and Al/Ca (-0.52) in the soil. In forests with the high input of atmospheric nitrogen (>2.0 kg NH+ 4/(ha yr) and >6.4 kg Nmin/(ha yr)), a tendency of decreasing Cmic, C/N, and Al/Ca, as well as increasing qCO2, was revealed, which could be indicative of deterioration in the functioning of microbial community and the chemical properties of the soil.

Atmospheric deposition of selected chemicals and their effect on nonpoint-source pollution in the Twin Cities Metropolitan Area, Minnesota

Science.gov (United States)

Brown, R.G.

1984-01-01

Atmospheric deposition and subsequent runoff concentrations of total Kjeldahl nitrogen, dissolved nitrite-plus-nitrate nitrogen, total phosphorus, total sulfate (only for atmospheric deposition), total chloride, and total lead were studied from April 1 to October 31, 1980, in one rural and three urban watersheds in the Twin Cities Metropolitan Area, Minnesota. Seasonal patterns of wetfall and dryfall generally were similar for all constituents except chloride in both rural and urban watersheds. Similarity between constituents and between rural and urban watersheds suggested that regional air masses transported from the Gulf of Mexico by frontal storm movements influence seasonal patterns of atmospheric deposition in the metropolitan area. Local influences such as industrial, agricultural, and vehicular air pollutants were found to influence the magnitude or rate of atmospheric deposition rather than the seasonal pattern. Chloride was primarily influenced by northwest frontal storms laden with coastal chloride. Local influences such as dust from road deicing salt dust are thought to have caused an increase in atmospheric chloride during June.

Responses of Carbon Dynamics to Nitrogen Deposition in Typical Freshwater Wetland of Sanjiang Plain

Directory of Open Access Journals (Sweden)

Yang Wang

2014-01-01

Full Text Available The effects of nitrogen deposition (N-deposition on the carbon dynamics in typical Calamagrostis angustifolia wetland of Sanjiang Plain were studied by a pot-culture experiment during two continuous plant growing seasons. Elevated atmospheric N-deposition caused significant increases in the aboveground net primary production and root biomass; moreover, a preferential partition of carbon to root was also observed. Different soil carbon fractions gained due to elevated N-deposition and their response intensities followed the sequence of labile carbon > dissolved organic carbon > microbial biomass carbon, and the interaction between N-deposition and flooded condition facilitated the release of different carbon fractions. Positive correlations were found between CO2 and CH4 fluxes and liable carbon contents with N-deposition, and flooded condition also tended to facilitate CH4 fluxes and to inhibit the CO2 fluxes with N-deposition. The increases in soil carbon fractions occurring in the nitrogen treatments were significantly correlated with increases in root, aboveground parts, total biomass, and their carbon uptake. Our results suggested that N-deposition could enhance the contents of active carbon fractions in soil system and carbon accumulation in plant of the freshwater wetlands.

An evaluation of dry deposition from the long range atmospheric dispersion

International Nuclear Information System (INIS)

Suh, K.S.; Kim, E.H.; Hwang, W.T.; Han, M.H.; Lee, H.S.; Lee, C.W.

2003-01-01

The dry deposition of pollutants released into the atmosphere must be evaluated to estimate the radiological dose of terrestrial plants and foodstuffs in the ecosystem. Especially, the atmospheric dispersion and dry deposition models have been widely developed to predict and minimize the radiological damage for the surrounding environment after the TMI-2 and the Chernobyl accidents. A Lagrangian particle model for the evaluation the long-range dispersion has been firstly developed in Korea since 2001. The particle tracking method was used for the estimation of the concentration distribution of the radioactive materials released into the atmosphere. The model is designed to estimate air concentration and ground deposition at distances up to some thousands of kilometers from the source point in the horizontal direction. The turbulent motion is considered to separate the treatment of particles within the mixing layer and above the mixing layer. Also, the dispersion model is designed to receive the results of the MM5 model being operated by KMA (Korea Meteorological Administration). The test run of the long-range dispersion model has been performed in the area which covered extends from 102.47deg E to 173.34deg E and from 12.27deg N to 53.72deg N in Northeast Asia. The release point of Cs-137 assumed in the east part of the China. The long range dispersion model has been firstly developed to estimate the radiological consequences against a nuclear accident. The model will be supplemented by the comparative study using the data of the ETEX experiments. (author)

Dissolved organic carbon in the precipitation of Seoul, Korea: Implications for global wet depositional flux of fossil-fuel derived organic carbon

Science.gov (United States)

Yan, Ge; Kim, Guebuem

2012-11-01

Precipitation was sampled in Seoul over a one-year period from 2009 to 2010 to investigate the sources and fluxes of atmospheric dissolved organic carbon (DOC). The concentrations of DOC varied from 15 μM to 780 μM, with a volume-weighted average of 94 μM. On the basis of correlation analysis using the commonly acknowledged tracers, such as vanadium, the combustion of fossil-fuels was recognized to be the dominant source. With the aid of air mass backward trajectory analyses, we concluded that the primary fraction of DOC in our precipitation samples originated locally in Korea, albeit the frequent long-range transport from eastern and northeastern China might contribute substantially. In light of the relatively invariant organic carbon to sulfur mass ratios in precipitation over Seoul and other urban regions around the world, the global magnitude of wet depositional DOC originating from fossil-fuels was calculated to be 36 ± 10 Tg C yr-1. Our study further underscores the potentially significant environmental impacts that might be brought about by this anthropogenically derived component of organic carbon in the atmosphere.

Effects of historical and modern mining on mercury deposition in southeastern Peru.

Science.gov (United States)

Beal, Samuel A; Jackson, Brian P; Kelly, Meredith A; Stroup, Justin S; Landis, Joshua D

2013-11-19

Both modern anthropogenic emissions of mercury (Hg), primarily from artisanal and small-scale gold mining (ASGM), and preindustrial anthropogenic emissions from mining are thought to have a large impact on present-day atmospheric Hg deposition. We study the spatial distribution of Hg and its depositional history over the past ∼400 years in sediment cores from lakes located regionally proximal (∼90-150 km) to the largest ASGM in Peru and distal (>400 km) to major preindustrial mining centers. Total Hg concentrations in surface sediments from fourteen lakes are typical of remote regions (10-115 ng g(-1)). Hg fluxes in cores from four lakes demonstrate preindustrial Hg deposition in southeastern Peru was spatially variable and at least an order of magnitude lower than previously reported fluxes in lakes located closer to mining centers. Average modern (A.D. 2000-2011) Hg fluxes in these cores are 3.4-6.9 μg m(-2) a(-1), compared to average preindustrial (A.D. 1800-1850) fluxes of 0.8-2.5 μg m(-2) a(-1). Modern Hg fluxes determined from the four lakes are on average 3.3 (±1.5) times greater than their preindustrial fluxes, similar to those determined in other remote lakes around the world. This agreement suggests that Hg emissions from ASGM are likely not significantly deposited in nearby down-wind regions.

Micrometeorological measurement of the dry deposition flux of sulphate and nitrate aerosols to coniferous forest

NARCIS (Netherlands)

Wyers, G.P.; Duyzer, J.H.

1997-01-01

Dry deposition fluxes of sulphate and nitrate have been determined over a coniferous canopy using the aerodynamic gradient technique. Vertical concentration gradients of sulphate and nitrate were measured with filters; the gradient of ammonium bisulphate was measured with thermodenuders. Filter

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.

Uncertainty analysis of atmospheric deposition simulation of radiocesium and radioiodine from Fukushima Daiichi Nuclear Power Plant

Science.gov (United States)

Morino, Yu; Ohara, Toshimasa; Yumimoto, Keiya

2014-05-01

Chemical transport models (CTM) played key roles in understanding the atmospheric behaviors and deposition patterns of radioactive materials emitted from the Fukushima Daiichi nuclear power plant (FDNPP) after the nuclear accident that accompanied the great Tohoku earthquake and tsunami on 11 March 2011. In this study, we assessed uncertainties of atmospheric simulation by comparing observed and simulated deposition of radiocesium (137Cs) and radioiodine (131I). Airborne monitoring survey data were used to assess the model performance of 137Cs deposition patterns. We found that simulation using emissions estimated with a regional-scale (~500 km) CTM better reproduced the observed 137Cs deposition pattern in eastern Japan than simulation using emissions estimated with local-scale (~50 km) or global-scale CTM. In addition, we estimated the emission amount of 137Cs from FDNPP by combining a CTM, a priori source term, and observed deposition data. This is the first use of airborne survey data of 137Cs deposition (more than 16,000 data points) as the observational constraints in inverse modeling. The model simulation driven by a posteriori source term achieved better agreements with 137Cs depositions measured by aircraft survey and at in-situ stations over eastern Japan. Wet deposition module was also evaluated. Simulation using a process-based wet deposition module reproduced the observations well, whereas simulation using scavenging coefficients showed large uncertainties associated with empirical parameters. The best-available simulation reproduced the observed 137Cs deposition rates in high-deposition areas (≥10 kBq m-2) within one order of magnitude. Recently, 131I deposition map was released and helped to evaluate model performance of 131I deposition patterns. Observed 131I/137Cs deposition ratio is higher in areas southwest of FDNPP than northwest of FDNPP, and this behavior was roughly reproduced by a CTM if we assume that released 131I is more in gas phase

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

Science.gov (United States)

Nelson, David M.; Tsunogai, Urumu; Ding, Dong; Ohyama, Takuya; Komatsu, Daisuke D.; Nakagawa, Fumiko; Noguchi, Izumi; Yamaguchi, Takashi

2018-05-01

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 be transported 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 ˜ +23 and +31 ‰ with higher values during winter and lower values in summer, which suggests the 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 and dry deposition in rural environments and wet deposition in urban 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

Return of the coral reef hypothesis: basin to shelf partitioning of CaCO3 and its effect on atmospheric CO2.

Science.gov (United States)

Opdyke, B N; Walker, J C

1992-08-01

Differences in the rate of coral reef carbonate deposition from the Pleistocene to the Holocene may account for the Quaternary variation of atmospheric CO2. Volumes of carbonate associated with Holocene reefs require an average deposition rate of 2.0 x 10(13) mol/yr for the past 5 ka. In light of combined riverine, midocean ridge, and ground-water fluxes of calcium to the oceans of 2.3 x 10(13) mol/yr, the current flux of calcium carbonate to pelagic sediments must be far below the Pleistocene average of 1.2 x 10(13) mol/yr. We suggest that sea-level change shifts the locus of carbonate deposition from the deep sea to the shelves as the normal glacial-interglacial pattern of deposition for Quaternary global carbonates. To assess the impact of these changes on atmospheric CO2, a simple numerical simulation of the global carbon cycle was developed. Atmospheric CO2 as well as calcite saturation depth and sediment responses to these carbonate deposition changes are examined. Atmospheric CO2 changes close to those observed in the Vostok ice core, approximately 80 ppm CO2, for the Quaternary are observed as well as the approximate depth changes in percent carbonate of sediments measured in the Pacific Ocean over the same time interval.

Prompt atmospheric neutrino fluxes: perturbative QCD models and nuclear effects

Energy Technology Data Exchange (ETDEWEB)

Bhattacharya, Atri [Department of Physics, University of Arizona,1118 E. 4th St. Tucson, AZ 85704 (United States); Space sciences, Technologies and Astrophysics Research (STAR) Institute,Université de Liège,Bât. B5a, 4000 Liège (Belgium); Enberg, Rikard [Department of Physics and Astronomy, Uppsala University,Box 516, SE-75120 Uppsala (Sweden); Jeong, Yu Seon [Department of Physics and IPAP, Yonsei University,50 Yonsei-ro Seodaemun-gu, Seoul 03722 (Korea, Republic of); National Institute of Supercomputing and Networking, KISTI,245 Daehak-ro, Yuseong-gu, Daejeon 34141 (Korea, Republic of); Kim, C.S. [Department of Physics and IPAP, Yonsei University,50 Yonsei-ro Seodaemun-gu, Seoul 03722 (Korea, Republic of); Reno, Mary Hall [Department of Physics and Astronomy, University of Iowa,Iowa City, Iowa 52242 (United States); Sarcevic, Ina [Department of Physics, University of Arizona,1118 E. 4th St. Tucson, AZ 85704 (United States); Department of Astronomy, University of Arizona,933 N. Cherry Ave., Tucson, AZ 85721 (United States); Stasto, Anna [Department of Physics, 104 Davey Lab, The Pennsylvania State University,University Park, PA 16802 (United States)

2016-11-28

We evaluate the prompt atmospheric neutrino flux at high energies using three different frameworks for calculating the heavy quark production cross section in QCD: NLO perturbative QCD, k{sub T} factorization including low-x resummation, and the dipole model including parton saturation. We use QCD parameters, the value for the charm quark mass and the range for the factorization and renormalization scales that provide the best description of the total charm cross section measured at fixed target experiments, at RHIC and at LHC. Using these parameters we calculate differential cross sections for charm and bottom production and compare with the latest data on forward charm meson production from LHCb at 7 TeV and at 13 TeV, finding good agreement with the data. In addition, we investigate the role of nuclear shadowing by including nuclear parton distribution functions (PDF) for the target air nucleus using two different nuclear PDF schemes. Depending on the scheme used, we find the reduction of the flux due to nuclear effects varies from 10% to 50% at the highest energies. Finally, we compare our results with the IceCube limit on the prompt neutrino flux, which is already providing valuable information about some of the QCD models.

Modelling land surface fluxes of CO2 in response to climate change and nitrogen deposition

DEFF Research Database (Denmark)

Hansen, Kristina; Ambelas Skjøth, Carsten; Geels, Camilla

Climate change, land use variations, and impacts of atmospheric nitrogen (N) deposition represent uncertainties for the prediction of future greenhouse gas exchange between land surfaces and the atmosphere as the mechanisms describing nutritional effects are not well developed in climate...... climate feedback mechanisms of CO2 between changes in management, land use practise, and climate change....

Atmospheric deposition of nitrogen to the Baltic Sea in the period 1995–2006

Directory of Open Access Journals (Sweden)

J. Bartnicki

2011-10-01

Full Text Available The EMEP/MSC-W model has been used to compute atmospheric nitrogen deposition into the Baltic Sea basin for the period of 12 yr: 1995–2006. The level of annual total nitrogen deposition into the Baltic Sea basin has changed from 230 Gg N in 1995 to 199 Gg N in 2006, decreasing 13 %. This value corresponds well with the total nitrogen emission reduction (11 % in the HELCOM Contracting Parties. However, inter-annual variability of nitrogen deposition to the Baltic Sea basin is relatively large, ranging from −13 % to +17 % of the averaged value. It is mainly caused by the changing meteorological conditions and especially precipitation in the considered period. The calculated monthly deposition pattern is similar for most of the years showing maxima in the autumn months October and November. The source allocation budget for atmospheric nitrogen deposition to the Baltic Sea basin was calculated for each year of the period 1997–2006. The main emission sources contributing to total nitrogen deposition are: Germany 18–22 %, Poland 11–13 % and Denmark 8–11 %. There is also a significant contribution from distant sources like the United Kingdom 6–9 %, as well as from the international ship traffic on the Baltic Sea 4–5 %.

Terrestrial mosses as biomonitors of atmospheric POPs pollution: a review.

Science.gov (United States)

Harmens, H; Foan, L; Simon, V; Mills, G

2013-02-01

Worldwide there is concern about the continuing release of persistent organic pollutants (POPs) into the environment. In this study we review the application of mosses as biomonitors of atmospheric deposition of POPs. Examples in the literature show that mosses are suitable organisms to monitor spatial patterns and temporal trends of atmospheric concentrations or deposition of POPs. These examples include polycyclic aromatic hydrocarbons (PAHs), polychlorobiphenyls (PCBs), dioxins and furans (PCDD/Fs), and polybrominated diphenyl ethers (PBDEs). The majority of studies report on PAHs concentrations in mosses and relative few studies have been conducted on other POPs. So far, many studies have focused on spatial patterns around pollution sources or the concentration in mosses in remote areas such as the polar regions, as an indication of long-range transport of POPs. Very few studies have determined temporal trends or have directly related the concentrations in mosses with measured atmospheric concentrations and/or deposition fluxes. Copyright © 2012 Elsevier Ltd. All rights reserved.

Atmospheric transport and deposition of pesticides: An assessment of current knowledge

DEFF Research Database (Denmark)

Pul, W.A.J. van; Bidleman, T.F.; Brorström-Lunden, E.

1999-01-01

The current knowledge on atmospheric transport and deposition of pesticides is reviewed and discussed by a working group of experts during the Workshop on Fate of pesticides in the atmosphere; implications for risk assessment, held in Driebergen, the Netherlands, 22-24 April, 1998. In general...... in the exchange processes at the interface between air and soil/water/vegetation. In all process descriptions the uncertainty in the physicochemical properties play an important role. Particularly those in the vapour pressure, Henry's law constant and its temperature dependency. More accurate data...

Rapid atmospheric transport and large-scale deposition of recently synthesized plant waxes

Science.gov (United States)

Nelson, Daniel B.; Ladd, S. Nemiah; Schubert, Carsten J.; Kahmen, Ansgar

2018-02-01

Sedimentary plant wax 2H/1H ratios are important tools for understanding hydroclimate and environmental changes, but large spatial and temporal uncertainties exist about transport mechanisms from ecosystem to sediments. To assess atmospheric pathways, we collected aerosol samples for two years at four locations within a ∼60 km radius in northern Switzerland. We measured n-alkane distributions and 2H/1H ratios in these samples, and from local plants, leaf litter, and soil, as well as surface sediment from six nearby lakes. Increased concentrations and 2H depletion of long odd chain n-alkanes in early summer aerosols indicate that most wax aerosol production occurred shortly after leaf unfolding, when plants synthesize waxes in large quantities. During autumn and winter, aerosols were characterized by degraded n-alkanes lacking chain length preferences diagnostic of recent biosynthesis, and 2H/1H values that were in some cases more than 100‰ higher than growing season values. Despite these seasonal shifts, modeled deposition-weighted average 2H/1H values of long odd chain n-alkanes primarily reflected summer values. This was corroborated by n-alkane 2H/1H values in lake sediments, which were similar to deposition-weighted aerosol values at five of six sites. Atmospheric deposition rates for plant n-alkanes on land were ∼20% of accumulation rates in lakes, suggesting a role for direct deposition to lakes or coastal oceans near similar production sources, and likely a larger role for deposition on land and transport in river systems. This mechanism allows mobilization and transport of large quantities of recently produced waxes as fine-grained material to low energy sedimentation sites over short timescales, even in areas with limited topography. Widespread atmospheric transfer well before leaf senescence also highlights the importance of the isotopic composition of early season source water used to synthesize waxes for the geologic record.

Critical Loads of Atmospheric Nitrogen Deposition for Aquatic Ecosystems in Yosemite and Sequoia and Kings Canyon National Parks

Science.gov (United States)

Nanus, L.; Clow, D. W.; Sickman, J. O.

2016-12-01

High-elevation aquatic ecosystems in Yosemite (YOSE) and Sequoia and Kings Canyon (SEKI) National Parks are impacted by atmospheric nitrogen (N) deposition associated with local and regional air pollution. Documented effects include elevated surface water nitrate concentrations, increased algal productivity, and changes in diatom species assemblages. Annual wet inorganic N deposition maps, developed at 1-km resolution for YOSE and SEKI to quantify N deposition to sensitive high-elevation ecosystems, range from 1.0 to over 5.0 kg N ha-1 yr-1. Critical loads of N deposition for nutrient enrichment of aquatic ecosystems were quantified and mapped using a geostatistical approach, with N deposition, topography, vegetation, geology, and climate as potential explanatory variables. Multiple predictive models were created using various combinations of explanatory variables; this approach allowed us to better quantify uncertainty and more accurately identify the areas most sensitive to atmospherically deposited N. The lowest critical loads estimates and highest exceedances identified within YOSE and SEKI occurred in high-elevation basins with steep slopes, sparse vegetation, and areas of neoglacial till and talus. These results are consistent with previous analyses in the Rocky Mountains, and highlight the sensitivity of alpine ecosystems to atmospheric N deposition.

Atmospheric CO2 inversions on the mesoscale using data-driven prior uncertainties: quantification of the European terrestrial CO2 fluxes

Science.gov (United States)

Kountouris, Panagiotis; Gerbig, Christoph; Rödenbeck, Christian; Karstens, Ute; Koch, Thomas F.; Heimann, Martin

2018-03-01

Optimized biogenic carbon fluxes for Europe were estimated from high-resolution regional-scale inversions, utilizing atmospheric CO2 measurements at 16 stations for the year 2007. Additional sensitivity tests with different data-driven error structures were performed. As the atmospheric network is rather sparse and consequently contains large spatial gaps, we use a priori biospheric fluxes to further constrain the inversions. The biospheric fluxes were simulated by the Vegetation Photosynthesis and Respiration Model (VPRM) at a resolution of 0.1° and optimized against eddy covariance data. Overall we estimate an a priori uncertainty of 0.54 GtC yr-1 related to the poor spatial representation between the biospheric model and the ecosystem sites. The sink estimated from the atmospheric inversions for the area of Europe (as represented in the model domain) ranges between 0.23 and 0.38 GtC yr-1 (0.39 and 0.71 GtC yr-1 up-scaled to geographical Europe). This is within the range of posterior flux uncertainty estimates of previous studies using ground-based observations.

Evaluating the Capacity of Global CO2 Flux and Atmospheric Transport Models to Incorporate New Satellite Observations

Science.gov (United States)

Kawa, S. R.; Collatz, G. J.; Erickson, D. J.; Denning, A. S.; Wofsy, S. C.; Andrews, A. E.

2007-01-01

As we enter the new era of satellite remote sensing for CO2 and other carbon cyclerelated quantities, advanced modeling and analysis capabilities are required to fully capitalize on the new observations. Model estimates of CO2 surface flux and atmospheric transport are required for initial constraints on inverse analyses, to connect atmospheric observations to the location of surface sources and sinks, and ultimately for future projections of carbon-climate interactions. For application to current, planned, and future remotely sensed CO2 data, it is desirable that these models are accurate and unbiased at time scales from less than daily to multi-annual and at spatial scales from several kilometers or finer to global. Here we focus on simulated CO2 fluxes from terrestrial vegetation and atmospheric transport mutually constrained by analyzed meteorological fields from the Goddard Modeling and Assimilation Office for the period 1998 through 2006. Use of assimilated meteorological data enables direct model comparison to observations across a wide range of scales of variability. The biospheric fluxes are produced by the CASA model at lxi degrees on a monthly mean basis, modulated hourly with analyzed temperature and sunlight. Both physiological and biomass burning fluxes are derived using satellite observations of vegetation, burned area (as in GFED-2), and analyzed meteorology. For the purposes of comparison to CO2 data, fossil fuel and ocean fluxes are also included in the transport simulations. In this presentation we evaluate the model's ability to simulate CO2 flux and mixing ratio variability in comparison to in situ observations at sites in Northern mid latitudes and the continental tropics. The influence of key process representations is inferred. We find that the model can resolve much of the hourly to synoptic variability in the observations, although there are limits imposed by vertical resolution of boundary layer processes. The seasonal cycle and its

Long-Term Simulated Atmospheric Nitrogen Deposition Alters Leaf and Fine Root Decomposition

Science.gov (United States)

Atmospheric nitrogen deposition has been suggested to increase forest carbon sequestration across much of the Northern Hemisphere; slower organic matter decomposition could contribute to this increase. At four sugar maple (Acer saccharum)-dominated northern hardwood forests, we p...

Atmospheric particle characterization, distribution, and deposition in Xi'an, Shaanxi Province, Central China

International Nuclear Information System (INIS)

Cao Zongze; Yang Yuhua; Lu, Julia; Zhang Chengxiao

2011-01-01

Physical characterization and chemical analysis of settled dusts collected in Xi'an from November 2007 to December 2008 show that (1) dust deposition rates ranged from 14.6 to 350.4 g m -2 yr -1 . The average deposition rate (76.7 g m -2 yr -1 ) ranks the 11th out of 56 dust deposition rates observed throughout the world. The coal-burning power was the major particle source; (2) on average (except site 4), ∼10% of the settled dusts having size 70% having size <30 μm; (3) the concentrations for 20 out of 27 elements analyzed were upto 18 times higher than their soil background values in China. With such high deposition rates of dusts that contain elevated levels of toxic elements, actions should be taken to reduce emission and studies are needed to assess the potential impacts of settled particles on surface ecosystem, water resource, and human health in the area. - Research highlights: → High atmospheric dust deposition rate in Xi'an, Shaanxi, China. → Coal-burning power plan being a major source of particulate matter in Xi'an area. → High levels of toxic elements in the settled dusts. → Enrichment of heavy metals (e.g., Pb, Ni, Cu) in fine particles. - Atmospheric dust deposition rate is high and the levels of toxic elements associated with the settled dusts are elevated in Xi'an, Shaanxi, China.

Atmospheric mercury accumulation between 5900 and 800 calibrated years BP in the high arctic of Canada recorded by Peat Hummocks

DEFF Research Database (Denmark)

Givelet, N.; Roos-Barraclough, F.; Goodsite, Michael Evan

2004-01-01

In this paper, we present the first comprehensive long-term record of preanthropogenic rates of atmospheric mercury accumulation in dated peat deposits for the High Arctic of Canada. Geochemical studies of two peat hummocks from Bathurst Island, Nunavut reveal substantial inputs from soil dust...... (titanium), marine aerosols (bromine), and mineral-water interactions (uranium). Mercury, however, was supplied to these peat mounds exclusively by atmospheric deposition. Mercury concentration measurements and age dating of the peat profiles indicate rather constant natural "background" mercury flux of ca....... 1 microgram per square meter per year from 5900 to 800 calibrated years BP. These values are well within the range of the mercury fluxes reported from other Arctic locations, but also by peat cores from southern Canada that provide a record of atmospheric Hg accumulation extending back 8000 years...

The atmospheric chemical vapour deposition of coatings on glass

International Nuclear Information System (INIS)

Sanderson, Kevin David

1996-01-01

The deposition of thin films of indium oxide, tin doped indium oxide (ITO) and titanium nitride for solar control applications have been investigated by Atmospheric Chemical Vapour Deposition (APCVD). Experimental details of the deposition system and the techniques used to characterise the films are presented. Results from investigations into the deposition parameters, the film microstructure and film material properties are discussed. A range of precursors were investigated for the deposition of indium oxide. The effect of pro-mixing the vaporised precursor with an oxidant source and the deposition temperature has been studied. Polycrystalline In 2 O 3 films with a resistivity of 1.1 - 3x10 -3 Ω cm were obtained with ln(thd) 3 , oxygen and nitrogen. The growth of ITO films from ln(thd) 3 , oxygen and a range of tin dopants is also presented. The effect of the dopant precursor, the doping concentration, deposition temperature and the effect of additives on film growth and microstructure is discussed. Control over the preferred orientation growth of ITO has been achieved by the addition of acetate species during film growth. Insitu infra-red spectroscopy has been used to identify the gas phase species and identify the species responsible for the film modification. ITO films with a resistivities of 1.5 - 4x10 -4 Ω cm have been achieved. The deposition of titanium nitride by the APCVD of Ti(NMe 2 ) 4 and a mixture of Ti(NMe 2 ) 4 and ammonia is reported. Contamination of the films and pro-reaction between the precursors in the gas phase is discussed, and the synthesis of new precursors for the deposition of titanium nitride is reported. New precursors have been synthesised under anaerobic conditions and characterised by infra-red spectroscopy, 1 H and 13 C NMR, mass spectrometry, thermal gravemetric analysis and three by single crystal X-ray diffraction. Deposition of titanium nitride utilising two new precursors is reported. (author)

Testing the FOODBANCS hypothesis: Seasonal variations in near-bottom particle flux, bioturbation intensity, and deposit feeding based on 234Th measurements

Science.gov (United States)

McClintic, Mark A.; DeMaster, David J.; Thomas, Carrie J.; Smith, Craig R.

2008-11-01

Naturally occurring 234Th (24-d half-life) was used on the West Antarctic continental shelf to evaluate temporal variations in the flux of particulate material reaching the seabed, bioturbation intensity, the seasonal continuity of feeding by benthic fauna, and trends in particle selection during ingestion for six common detritivores (four surface deposit feeders and two subsurface deposit feeders). These measurements were made at three stations during the five FOODBANCS cruises (December 1999, March, June, and October 2000, and March 2001) to assess the nature of pelagic-benthic coupling on the shelf and to evaluate the seabed as a potential food bank for deposit feeders when surface primary production is minimal. Two summer regimes were sampled (March 2000 and March 2001) with the latter exhibiting a distinct 1-2-cm-thick phytodetritus layer in nearly all sediment core samples. At site B, the 234Th fluxes into the near-bottom (150/170 mab) sediment traps were indistinguishable for the December-March 2000, March-June 2000, and June-October 2000 sampling intervals (fluxes ranging from 170 to 280 dpm m -2 d -1). However, the sediment-trap 234Th flux measured for the October 2000-March 2001 interval (1000 dpm m -2 d -1) was ˜5-fold greater than during the other three sampling periods, consistent with the deposition of a phytodetritus layer. The steady-state 234Th fluxes derived from seabed inventories at site B were 2.4-2.7 times greater than the sediment-trap 234Th fluxes, indicating substantial scavenging of this particle-reactive radiotracer in the bottom 150 m of the water column and/or lateral transport near the seabed. The seabed 234Th inventories at the three stations showed no variation during the first four cruises, but were significantly greater during cruise FB-V (March 2001), when the phytodetritus layer occurred. Based on 234Th distributions in the seabed, bioturbation intensities (quantified using the diffusive mixing coefficient, Db) varied from 0

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

The long term recovery of heat and moisture fluxes to the atmosphere following fire in Australia's tropical savanna

Science.gov (United States)

Tapper, N.; Beringer, J.; Hutley, L.; Coutts, A.

2003-04-01

Fire is probably the greatest natural and anthropogenic environmental disturbance in Australia's tropical savannas, with the vast area burned each year (up to 250,000 km^2) likely to increase with predicted regional climate change. Globally savanna ecosystems cover 11.5% of the global landscape (Scholes and Hall 1996). As much as 75% of this landscape burns annually (Hao et al., 1990), accounting for more than 40% of all global biomass consumed (Hao and Ward 1993). These landscape-scale fires undoubtedly have massive impacts on regional water, energy and carbon dioxide exchanges and as a result may have important feedbacks to the atmosphere and regional climate. Fire may influence climate directly through the emission of smoke and trace gases from burning, but there are other important impacts of fire that may affect the atmosphere. Fire and the subsequent fire scars are likely to radically alter the surface energy budgets of tropical savannas through reduced surface albedo, increased available energy for partitioning into the convective fluxes, and increased substrate heat flux. The aerodynamic and biological properties of the ecosystem may also change, affecting surface-atmosphere coupling. There is a clear potential to influence atmospheric motion and moist convection at a range of scales. Potential fire scar impacts such as those mentioned above have previously been largely ignored and are the focus of the Savanna Fire Experiment (SAFE). Tower measurements of radiation, heat, moisture and CO_2 fluxes above burned and unburned savanna near Darwin, Australia, were initiated in August 2001 to observe the impacts of fire and fire scarring on flux exchange with the atmosphere, along with the longer term post-fire recovery of fluxes. Intensive field campaigns were mounted in the dry (fire) seasons of both 2001 and 2002, with flux recovery observed into the each of the subsequent monsoon seasons. Results and an early analysis of the time series of heat and moisture

Contribution of atmospheric nitrogen deposition to diffuse pollution in a typical hilly red soil catchment in southern China.

Science.gov (United States)

Shen, Jianlin; Liu, Jieyun; Li, Yong; Li, Yuyuan; Wang, Yi; Liu, Xuejun; Wu, Jinshui

2014-09-01

Atmospheric nitrogen (N) deposition is currently high and meanwhile diffuse N pollution is also serious in China. The correlation between N deposition and riverine N export and the contribution of N deposition to riverine N export were investigated in a typical hilly red soil catchment in southern China over a two-year period. N deposition was as high as 26.1 to 55.8kgN/(ha·yr) across different land uses in the studied catchment, while the riverine N exports ranged from 7.2 to 9.6kgN/(ha·yr) in the forest sub-catchment and 27.4 to 30.3kgN/(ha·yr) in the agricultural sub-catchment. The correlations between both wet N deposition and riverine N export and precipitation were highly positive, and so were the correlations between NH4(+)-N or NO3(-)-N wet deposition and riverine NH4(+)-N or NO3(-)-N exports except for NH4(+)-N in the agricultural sub-catchment, indicating that N deposition contributed to riverine N export. The monthly export coefficients of atmospheric deposited N from land to river in the forest sub-catchment (with a mean of 14%) presented a significant positive correlation with precipitation, while the monthly contributions of atmospheric deposition to riverine N export (with a mean of 18.7% in the agricultural sub-catchment and a mean of 21.0% in the whole catchment) were significantly and negatively correlated with precipitation. The relatively high contribution of N deposition to diffuse N pollution in the catchment suggests that efforts should be done to control anthropogenic reactive N emissions to the atmosphere in hilly red soil regions in southern China. Copyright © 2014. Published by Elsevier B.V.

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

Carbon Flux to the Atmosphere from Land-Use Changes: 1850 to 1990

Energy Technology Data Exchange (ETDEWEB)

Houghton, R.A.

2001-02-22

The database documented in this numeric data package, a revision to a database originally published by the Carbon Dioxide Information Analysis Center (CDIAC) in 1995, consists of annual estimates, from 1850 through 1990, of the net flux of carbon between terrestrial ecosystems and the atmosphere resulting from deliberate changes in land cover and land use, especially forest clearing for agriculture and the harvest of wood for wood products or energy. The data are provided on a year-by-year basis for nine regions (North America, South and Central America, Europe, North Africa and the Middle East, Tropical Africa, the Former Soviet Union, China, South and Southeast Asia, and the Pacific Developed Region) and the globe. Some data begin earlier than 1850 (e.g., for six regions, areas of different ecosystems are provided for the year 1700) or extend beyond 1990 (e.g., fuelwood harvest in South and Southeast Asia, by forest type, is provided through 1995). The global net flux during the period 1850 to 1990 was 124 Pg of carbon (1 petagram = 10{sup 15} grams). During this period, the greatest regional flux was from South and Southeast Asia (39 Pg of carbon), while the smallest regional flux was from North Africa and the Middle East (3 Pg of carbon). For the year 1990, the global total net flux was estimated to be 2.1 Pg of carbon.

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.

A Carbon Flux Super Site. New Insights and Innovative Atmosphere-Terrestrial Carbon Exchange Measurements and Modeling

Energy Technology Data Exchange (ETDEWEB)

Leclerc, Monique Y. [The University of Georgia Research Foundation, Athens, GA (United States)

2014-11-17

This final report presents the main activities and results of the project “A Carbon Flux Super Site: New Insights and Innovative Atmosphere-Terrestrial Carbon Exchange Measurements and Modeling” from 10/1/2006 to 9/30/2014. It describes the new AmeriFlux tower site (Aiken) at Savanna River Site (SC) and instrumentation, long term eddy-covariance, sodar, microbarograph, soil and other measurements at the site, and intensive field campaigns of tracer experiment at the Carbon Flux Super Site, SC, in 2009 and at ARM-CF site, Lamont, OK, and experiments in Plains, GA. The main results on tracer experiment and modeling, on low-level jet characteristics and their impact on fluxes, on gravity waves and their influence on eddy fluxes, and other results are briefly described in the report.

Puff-plume atmospheric deposition model for use at SRP in emergency-response situations

International Nuclear Information System (INIS)

Garrett, A.J.; Murphy, C.E. Jr.

1981-05-01

An atmospheric transport and diffusion model developed for real-time calculation of the location and concentration of toxic or radioactive materials during an accidental release was improved by including deposition calculations

Atmospheric deposition as a source of carbon and nutrients to barren, alpine soils of the Colorado Rocky Mountains

Science.gov (United States)

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

2012-03-01

Many alpine areas are experiencing intense deglaciation, biogeochemical changes driven by temperature rise, and changes in atmospheric deposition. There is mounting evidence that the water quality of alpine streams may be related to these changes, including rising atmospheric deposition of carbon (C) and nutrients. Given that barren alpine soils can be severely C limited, we evaluated the magnitude and chemical quality of atmospheric deposition of C and nutrients to an alpine site, the Green Lake 4 catchment in the Colorado Rocky Mountains. Using a long term dataset (2002-2010) of weekly atmospheric wet deposition and snowpack chemistry, we found that volume weighted mean dissolved organic carbon (DOC) concentrations were approximately 1.0 mg L-1and weekly concentrations reached peaks as high at 6-10 mg L-1 every summer. Total dissolved nitrogen concentration also peaked in the summer, whereas total dissolved phosphorus and calcium concentrations were highest in the spring. Relationships among DOC concentration, dissolved organic matter (DOM) fluorescence properties, and nitrate and sulfate concentrations suggest that pollutants from nearby urban and agricultural sources and organic aerosols derived from sub-alpine vegetation may influence high summer DOC wet deposition concentrations. Interestingly, high DOC concentrations were also recorded during "dust-in-snow" events in the spring. Detailed chemical and spectroscopic analyses conducted for samples collected in 2010 revealed that the DOM in many late spring and summer samples was less aromatic and polydisperse and of lower molecular weight than that of winter and fall samples and, therefore, likely to be more bioavailable to microbes in barren alpine soils. Bioavailability experiments with different types of atmospheric C sources are needed to better evaluate the substrate quality of atmospheric C inputs. Our C budget estimates for the Green Lake 4 catchment suggest that atmospheric deposition represents an

Interlaboratory model comparisons of atmospheric concentrations with and without deposition

International Nuclear Information System (INIS)

Kern, C.D.; Cooper, R.E.

1978-01-01

To calculate the dose to the regional and U.S. populations, the pollutant concentration both with and without deposition and the amount of material deposited on the ground and watersheds around such a facility must be known. The following report (Article 50) of this document contains some initial estimates of population exposure from atmospheric effluents. The expertise of laboratories supported by U.S. Department of Energy funds ensures that the latest methods and data are available. Lawrence Livermore Laboratory (LLL) performed regional calculations (out to distances of the order of 200 km from a hypothetical fuel reprocessing plant). The Air Resources Laboratory (ARL) of the National Oceanic and Atmospheric Administration (NOAA), and Battelle Pacific Northwest Laboratories (PNL) performed U.S. scale calculations, and ARL also did the global calculations. Data from a winter and summer period were used to make comparisons of calculations by LLL, ARL, and PNL to determine which model should be used for the final calculations and to determine if a 200-km square area centered on the site would be large enough for dose calculations via the water and food pathways

Stable isotope evidence for an atmospheric origin of desert nitrate deposits in northern Chile and southern California, U.S.A.

Science.gov (United States)

Böhlke, J.K.; Ericksen, G.E.; Revesz, K.

1997-01-01

Natural surficial accumulations of nitrate-rich salts in the Atacama Desert, northern Chile, and in the Death Valley region of the Mojave Desert, southern California, are well known, but despite many geologic and geochemical studies, the origins of the nitrates have remained controversial. N and O isotopes in nitrate, and S isotopes in coexisting soluble sulfate, were measured to determine if some proposed N sources could be supported or rejected, and to determine if the isotopic signature of these natural deposits could be used to distinguish them from various types of anthropogenic nitrate contamination that might be found in desert groundwaters. High-grade caliche-type nitrate deposits from both localities have ??15N values that range from -5 to +5???, but are mostly near 0???. Values of ??15N near 0??? are consistent with either bulk atmospheric N deposition or microbial N fixation as major sources of the N in the deposits. ??18O values of those desert nitrates with ??15N near 0??? range from about +31 to + 50??? (V-SMOW), significantly higher than that of atmospheric O2 (+ 23.5???). Such high values of ??18O are considered unlikely to result entirely from nitrification of reduced N, but rather resemble those of modern atmospheric nitrate in precipitation from some other localities. Assuming that limited modern atmospheric isotope data are applicable to the deposits, and allowing for nitrification of co-deposited ammonium, it is estimated that the fraction of the nitrate in the deposits that could be accounted for isotopically by atmospheric N deposition may be at least 20% and possibly as much as 100%. ??34S values are less diagnostic but could also be consistent with atmospheric components in some of the soluble sulfates associated with the deposits. The stable isotope data support the hypothesis that some high-grade caliche-type nitrate-rich salt deposits in some of the Earth's hyperarid deserts represent long-term accumulations of atmospheric deposition

GEM-CEDAR Challenge: Poynting Flux at DMSP and Modeled Joule Heat

Science.gov (United States)

Rastaetter, Lutz; Shim, Ja Soon; Kuznetsova, Maria M.; Kilcommons, Liam M.; Knipp, Delores J.; Codrescu, Mihail; Fuller-Rowell, Tim; Emery, Barbara; Weimer, Daniel R.; Cosgrove, Russell;

Trace-element evidence for the origin of desert varnish by direct aqueous atmospheric deposition

Science.gov (United States)

Thiagarajan, Nivedita; Aeolus Lee, Cin-Ty

2004-07-01

Smooth rock surfaces in arid environments are often covered with a thin coating of Fe-Mn oxyhydroxides known as desert varnish. It is debated whether such varnish is formed (a) by slow diagenesis of dust particles deposited on rock surfaces, (b) by leaching from the underlying rock substrate, or (c) by direct deposition of dissolved constituents in the atmosphere. Varnishes collected from smooth rock surfaces in the Mojave Desert and Death Valley, California are shown here to have highly enriched and fractionated trace-element abundances relative to upper continental crust (UCC). They are highly enriched in Co, Ni, Pb and the rare-earth elements (REEs). In particular, they have anomalously high Ce/La and low Y/Ho ratios. These features can only be explained by preferential scavenging of Co, Ni, Pb and the REEs by Fe-Mn oxyhydroxides in an aqueous environment. High field strength elements (HFSEs: Zr, Hf, Ta, Nb, Th), however, show only small enrichments despite the fact that these elements should also be strongly scavenged by Fe-Mn oxyhydroxides. This suggests that their lack of enrichment is a feature inherited from a solution initially poor in HFSEs. The first two scenarios for varnish formation can be ruled out as follows. The high enrichment factors of Fe, Mn and many trace elements cannot be generated by mass loss associated with post-depositional diagenesis of dust particles because such a process predicts only a small increase in concentration. In addition, the highly fractionated abundance patterns of particle reactive element pairs (e.g., Ce/La and Y/Ho) rules out leaching of the rock substrate. This is because if leaching were to occur, varnishes would grow from the inside to the outside, and thus any particle-reactive trace element leached from the substrate would be quantitatively sequestered in the Fe-Mn oxyhydroxide layers, prohibiting any significant elemental fractionations. One remaining possibility is that the Fe, Mn and trace metals in varnish are

The effects of atmospheric nitrogen deposition on terrestrial and freshwater biodiversity

Science.gov (United States)

Baron, Jill S.; Barber, Mary C.; Adams, Mark; Agboola, Julius I.; Allen, Edith B.; Bealey, William J.; Bobbink, Roland; Bobrovsky, Maxim V.; Bowman, William D.; Branquinho, Cristina; Bustamente, Mercedes M. C.; Clark, Christopher M.; Cocking, Edward C.; Cruz, Cristina; Davidson, Eric A.; Denmead, O. Tom; Dias, Teresa; Dise, Nancy B.; Feest, Alan; Galloway, James N.; Geiser, Linda H.; Gilliam, Frank S.; Harrison, Ian J.; Khanina, Larisa G.; Lu, Xiankai; Manrique, Esteban; Ochoa-Hueso, Raul; Ometto, Jean P. H. B.; Payne, Richard; Scheuschner, Thomas; Sheppard, Lucy J.; Simpson, Gavin L.; Singh, Y. V.; Stevens, Carly J.; Strachan, Ian; Sverdrup, Harald; Tokuchi, Naoko; van Dobben, Hans; Woodin, Sarah

2014-01-01

This chapter reports the findings of a Working Group on how atmospheric nitrogen (N) deposition affects both terrestrial and freshwater biodiversity. Regional and global scale impacts on biodiversity are addressed, together with potential indicators. Key conclusions are that: the rates of loss in biodiversity are greatest at the lowest and initial stages of N deposition increase; changes in species compositions are related to the relative amounts of N, carbon (C) and phosphorus (P) in the plant soil system; enhanced N inputs have implications for C cycling; N deposition is known to be having adverse effects on European and North American vegetation composition; very little is known about tropical ecosystem responses, while tropical ecosystems are major biodiversity hotspots and are increasingly recipients of very high N deposition rates; N deposition alters forest fungi and mycorrhyzal relations with plants; the rapid response of forest fungi and arthropods makes them good indicators of change; predictive tools (models) that address ecosystem scale processes are necessary to address complex drivers and responses, including the integration of N deposition, climate change and land use effects; criteria can be identified for projecting sensitivity of terrestrial and aquatic ecosystems to N deposition. Future research and policy-relevant recommendations are identified.

Use of mosses as biomonitors of atmospheric deposition of trace elements

International Nuclear Information System (INIS)

Steinnes, E.

2000-01-01

Some basic facts about the use of mosses as biomonitors of atmospheric trace element deposition are reviewed, and advantages and limitations of this approach are discussed, largely on the basis of experience from regular use of this technique in Norway over the last 20 years. Topics discussed include different versions of the moss technique, mechanisms and efficiencies of trace element uptake, conversion of concentrations in moss to bulk deposition rates, and contribution from sources other than air pollution to the elemental composition of different elements. Suggestions are presented for further work in order to extend the use of mosses as biomonitors. (author)