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.

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).

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

Directory of Open Access Journals (Sweden)

Y. Fu

2017-11-01

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

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.

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

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 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.

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 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).

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 %.

Spatial variation of mercury bioaccumulation in bats of Canada linked to atmospheric mercury deposition.

Science.gov (United States)

Chételat, John; Hickey, M Brian C; Poulain, Alexandre J; Dastoor, Ashu; Ryjkov, Andrei; McAlpine, Donald; Vanderwolf, Karen; Jung, Thomas S; Hale, Lesley; Cooke, Emma L L; Hobson, Dave; Jonasson, Kristin; Kaupas, Laura; McCarthy, Sara; McClelland, Christine; Morningstar, Derek; Norquay, Kaleigh J O; Novy, Richard; Player, Delanie; Redford, Tony; Simard, Anouk; Stamler, Samantha; Webber, Quinn M R; Yumvihoze, Emmanuel; Zanuttig, Michelle

2018-06-01

Wildlife are exposed to neurotoxic mercury at locations distant from anthropogenic emission sources because of long-range atmospheric transport of this metal. In this study, mercury bioaccumulation in insectivorous bat species (Mammalia: Chiroptera) was investigated on a broad geographic scale in Canada. Fur was analyzed (n=1178) for total mercury from 43 locations spanning 20° latitude and 77° longitude. Total mercury and methylmercury concentrations in fur were positively correlated with concentrations in internal tissues (brain, liver, kidney) for a small subset (n=21) of little brown bats (Myotis lucifugus) and big brown bats (Eptesicus fuscus), validating the use of fur to indicate internal mercury exposure. Brain methylmercury concentrations were approximately 10% of total mercury concentrations in fur. Three bat species were mainly collected (little brown bats, big brown bats, and northern long-eared bats [M. septentrionalis]), with little brown bats having lower total mercury concentrations in their fur than the other two species at sites where both species were sampled. On average, juvenile bats had lower total mercury concentrations than adults but no differences were found between males and females of a species. Combining our dataset with previously published data for eastern Canada, median total mercury concentrations in fur of little brown bats ranged from 0.88-12.78μg/g among 11 provinces and territories. Highest concentrations were found in eastern Canada where bats are most endangered from introduced disease. Model estimates of atmospheric mercury deposition indicated that eastern Canada was exposed to greater mercury deposition than central and western sites. Further, mean total mercury concentrations in fur of adult little brown bats were positively correlated with site-specific estimates of atmospheric mercury deposition. This study provides the largest geographic coverage of mercury measurements in bats to date and indicates that atmospheric

Oceanic Emissions and Atmospheric Depositions of Volatile Organic Compounds

Science.gov (United States)

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

2015-12-01

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

Attributes for MRB_E2RF1 Catchments by Major River Basins in the Conterminous United States: Normalized Atmospheric Deposition for 2002, Total Inorganic Nitrogen

Science.gov (United States)

Wieczorek, Michael; LaMotte, Andrew E.

2010-01-01

This tabular data set represents the average normalized atmospheric (wet) deposition, in kilograms per square kilometer multiplied by 100, of Total Inorganic Nitrogen for the year 2002 compiled for every MRB_E2RF1 catchment of selected Major River Basins (MRBs, Crawford and others, 2006). Estimates of Total Inorganic Nitrogen deposition are based on National Atmospheric Deposition Program (NADP) measurements (B. Larsen, U.S. Geological Survey, written. commun., 2007). De-trending methods applied to the year 2002 are described in Alexander and others, 2001. NADP site selection met the following criteria: stations must have records from 1995 to 2002 and have a minimum of 30 observations. The MRB_E2RF1 catchments are based on a modified version of the U.S. Environmental Protection Agency's (USEPA) ERF1_2 and include enhancements to support national and regional-scale surface-water quality modeling (Nolan and others, 2002; Brakebill and others, 2011). Data were compiled for every MRB_E2RF1 catchment for the conterminous United States covering New England and Mid-Atlantic (MRB1), South Atlantic-Gulf and Tennessee (MRB2), the Great Lakes, Ohio, Upper Mississippi, and Souris-Red-Rainy (MRB3), the Missouri (MRB4), the Lower Mississippi, Arkansas-White-Red, and Texas-Gulf (MRB5), the Rio Grande, Colorado, and the Great basin (MRB6), the Pacific Northwest (MRB7) river basins, and California (MRB8).

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.

Nitrogen concentrations in mosses indicate the spatial distribution of atmospheric nitrogen deposition in Europe

International Nuclear Information System (INIS)

Harmens, H.; Norris, D.A.; Cooper, D.M.; Mills, G.; Steinnes, E.; Kubin, E.; Thoeni, L.; Aboal, J.R.; Alber, R.; Carballeira, A.; Coskun, M.; De Temmerman, L.; Frolova, M.; Gonzalez-Miqueo, L.

2011-01-01

In 2005/6, nearly 3000 moss samples from (semi-)natural location across 16 European countries were collected for nitrogen analysis. The lowest total nitrogen concentrations in mosses ( 2 = 0.91) linear relationship was found between the total nitrogen concentration in mosses and measured site-specific bulk nitrogen deposition rates. The total nitrogen concentrations in mosses complement deposition measurements, helping to identify areas in Europe at risk from high nitrogen deposition at a high spatial resolution. - Highlights: → Nitrogen concentrations in mosses were determined at ca. 3000 sites across Europe. → Moss concentrations were compared with EMEP modelled nitrogen deposition. → The asymptotic relationship for Europe showed saturation at ca. 15 kg N ha -1 y -1 . → Linear relationships were found with measured nitrogen deposition in some countries. → Moss concentrations complement deposition measurements at high spatial resolution. - Mosses as biomonitors of atmospheric nitrogen deposition in Europe.

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 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

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

Atmospheric Deposition Modeling Results

Data.gov (United States)

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

Mapping background values of atmospheric nitrogen total depositions in Germany based on EMEP deposition modelling and the European Moss Survey 2005; Kartierung der Hintergrundwerte atmosphaerischer Stickstoff-Gesamtdepositionen in Deutschland anhand von Daten des EMEP-Messnetzes und des ICP Vegetation Moos-Monitoring 2005

Energy Technology Data Exchange (ETDEWEB)

Schroeder, Winfried; Holy, Marcel; Pesch, Roland [University of Vechta, Chair of Landscape Ecology, P.O.B. 1553, Vechta (Germany); Harmens, Harry [Environment Centre Wales, Centre for Ecology and Hydrology, Bangor, Gwynedd (United Kingdom); Fagerli, Hilde [Norwegian Meteorological Institute, Meteorological Synthesizing Centre-West of EMEP, P.O. Box 43-Blindern, Oslo (Norway)

2011-12-15

In order to map exceedances of critical atmospheric deposition loads for nitrogen (N) surface data on the atmospheric deposition of N compounds to terrestrial ecosystems are needed. Across Europe such information is provided by the international European Monitoring and Evaluation Programme (EMEP) in a resolution of 50 km by 50 km, relying on both emission data and measurement data on atmospheric depositions. The objective of the article at hand is on the improvement of the spatial resolution of the EMEP maps by combining them with data on the N concentration in mosses provided by the International Cooperative Programme on Effects of Air Pollution on Natural Vegetation and Crops (ICP Vegetation) of the United Nations Economic Commission for Europe (UNECE) Long-range Transboundary Air Pollution (LTRAP). Methods The map on atmospheric depositions of total N as modelled by EMEP was intersected with geostatistical surface estimations on the N concentration in mosses at a resolution of 5 km by 5 km. The medians of the N estimations in mosses were then calculated for each 50 km by 50 km grid cell. Both medians of moss estimations and corresponding modelled deposition values were ln-transformed and their relationship investigated and modelled by linear regression analysis. The regression equations were applied on the moss kriging estimates of the N concentration in mosses. The respective residuals were projected onto the centres of the EMEP grid cells and were mapped using variogram analysis and kriging procedures. Finally, the residual and the regression map were summed up to the map of total N deposition in terrestrial ecosystems throughout Europe. The regression analysis of the estimated N concentrations in mosses and the modelled EMEP depositions resulted in clear linear regression patterns with coefficients of determination of r{sup 2}=0.62 and Pearson correlations of r{sub p}=0.79 and Spearman correlations of r{sub s}=0.70, respectively. Regarding the German

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.

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.

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.

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)

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

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

Science.gov (United States)

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

2018-03-01

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

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

Science.gov (United States)

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

2012-08-01

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

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

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.

Total Sulfur Deposition (wet+dry) from the Atmosphere

Data.gov (United States)

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

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

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....

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.

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

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

Directory of Open Access Journals (Sweden)

Garth W. Redfield

2002-01-01

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

Atmospheric deposition 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

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

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.

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)

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

Nitrogen concentrations in mosses indicate the spatial distribution of atmospheric nitrogen deposition in Europe

Energy Technology Data Exchange (ETDEWEB)

Harmens, H., E-mail: hh@ceh.ac.uk [Centre for Ecology and Hydrology, Environment Centre Wales, Deiniol Road, Bangor, Gwynedd LL57 2UW (United Kingdom); Norris, D.A., E-mail: danor@ceh.ac.uk [Centre for Ecology and Hydrology, Environment Centre Wales, Deiniol Road, Bangor, Gwynedd LL57 2UW (United Kingdom); Cooper, D.M., E-mail: cooper@ceh.ac.uk [Centre for Ecology and Hydrology, Environment Centre Wales, Deiniol Road, Bangor, Gwynedd LL57 2UW (United Kingdom); Mills, G., E-mail: gmi@ceh.ac.uk [Centre for Ecology and Hydrology, Environment Centre Wales, Deiniol Road, Bangor, Gwynedd LL57 2UW (United Kingdom); Steinnes, E., E-mail: Eiliv.Steinnes@chem.ntnu.no [Department of Chemistry, Norwegian University of Science and Technology, 7491 Trondheim (Norway); Kubin, E., E-mail: Eero.Kubin@metla.fi [Finnish Forest Research Institute, Kirkkosaarentie 7, 91500 Muhos (Finland); Thoeni, L., E-mail: lotti.thoeni@fub-ag.ch [FUB-Research Group for Environmental Monitoring, Alte Jonastrasse 83, 8640 Rapperswil (Switzerland); Aboal, J.R., E-mail: jesusramon.aboal@usc.es [University of Santiago de Compostela, Faculty of Biology, Department of Ecology, 15782 Santiago de Compostela (Spain); Alber, R., E-mail: Renate.Alber@provinz.bz.it [Environmental Agency of Bolzano, 39055 Laives (Italy); Carballeira, A., E-mail: alejo.carballeira@usc.es [University of Santiago de Compostela, Faculty of Biology, Department of Ecology, 15782 Santiago de Compostela (Spain); Coskun, M., E-mail: coskunafm@yahoo.com [Canakkale Onsekiz Mart University, Faculty of Medicine, Department of Medical Biology, 17100 Canakkale (Turkey); De Temmerman, L., E-mail: ludet@var.fgov.be [Veterinary and Agrochemical Research Centre, Tervuren (Belgium); Frolova, M., E-mail: marina.frolova@lvgma.gov.lv [Latvian Environment, Geology and Meteorology Agency, Riga (Latvia); Gonzalez-Miqueo, L., E-mail: lgonzale2@alumni.unav.es [Univ. of Navarra, Irunlarrea No 1, 31008 Pamplona (Spain)

2011-10-15

In 2005/6, nearly 3000 moss samples from (semi-)natural location across 16 European countries were collected for nitrogen analysis. The lowest total nitrogen concentrations in mosses (<0.8%) were observed in northern Finland and northern UK. The highest concentrations ({>=}1.6%) were found in parts of Belgium, France, Germany, Slovakia, Slovenia and Bulgaria. The asymptotic relationship between the nitrogen concentrations in mosses and EMEP modelled nitrogen deposition (averaged per 50 km x 50 km grid) across Europe showed less scatter when there were at least five moss sampling sites per grid. Factors potentially contributing to the scatter are discussed. In Switzerland, a strong (r{sup 2} = 0.91) linear relationship was found between the total nitrogen concentration in mosses and measured site-specific bulk nitrogen deposition rates. The total nitrogen concentrations in mosses complement deposition measurements, helping to identify areas in Europe at risk from high nitrogen deposition at a high spatial resolution. - Highlights: > Nitrogen concentrations in mosses were determined at ca. 3000 sites across Europe. > Moss concentrations were compared with EMEP modelled nitrogen deposition. > The asymptotic relationship for Europe showed saturation at ca. 15 kg N ha{sup -1} y{sup -1}. > Linear relationships were found with measured nitrogen deposition in some countries. > Moss concentrations complement deposition measurements at high spatial resolution. - Mosses as biomonitors of atmospheric nitrogen deposition in Europe.

Net atmospheric mercury deposition to Svalbard: Estimates from lacustrine sediments

Science.gov (United States)

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

2012-11-01

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

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

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

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.

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

Science.gov (United States)

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

2012-09-01

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

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

Science.gov (United States)

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

2017-12-01

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

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...

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)

Atmospheric transport, diffusion, and deposition of radioactivity

International Nuclear Information System (INIS)

Crawford, T.V.

1969-01-01

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

Atmospheric transport, diffusion, and deposition of radioactivity

Energy Technology Data Exchange (ETDEWEB)

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

1969-07-01

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

Deposition 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.

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

Science.gov (United States)

Jiao, Linlin; Wang, Xunming; Li, Danfeng

2018-06-01

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

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.

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

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)

Depositional characteristics of atmospheric polybrominated diphenyl ethers on tree barks.

Science.gov (United States)

Chun, Man Young

2014-07-17

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

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.

Modelling atmospheric deposition flux of Cadmium and Lead in urban areas

International Nuclear Information System (INIS)

Cherin, Nicolas

2017-01-01

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

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.

Global Atmosphere Watch Workshop on Measurement-Model Fusion for Global Total Atmospheric Deposition (MMF-GTAD)

Science.gov (United States)

The World Meteorological Organization’s (WMO) Global Atmosphere Watch (GAW) Programme coordinates high-quality observations of atmospheric composition from global to local scales with the aim to drive high-quality and high-impact science while co-producing a new generation of pro...

Global Atmosphere Watch Workshop on Measurement-Model ...

Science.gov (United States)

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

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

A Heavy Metal Atmospheric Deposition Study in the South Ural Mountains

CERN Document Server

Frontasyeva, M V; Steinnes, E; Lyapunov, S M; Cherchintsev, V D

2002-01-01

Samples of the mosses Hylocomium splendens and Pleurozium schreberi, collected in the summer of 1998, were used to study the atmospheric deposition of heavy metals and other toxic elements in the Chelyabinsk Region situated in the South Ural, one of the most heavily polluted industrial areas of the Russian Federation. Samples of natural soils were collected simultaneously with moss at the same 30 sites in order to investigate surface accumulation of heavy metals and to examine the correlation of elements in moss and soil samples in order to separate contributions from atmospheric deposition and from soil minerals. A total of 38 elements (Na, Mg, Al, K, Ca, Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Zn, As, Se, Rb, Sr, Zr, Mo, Sb, Cs, Ba, La, Ce, Nd, Sm, Eu, Gd, Tb, Dy, Yb, Hf, Ta, W, Au, Th, U) in soil and 33 elements (Na, Mg, Al, Cl, K, Ca, Sc, V, Cr, Mn, Fe, Co, Ni, Zn, As, Se, Br, Rb, Ag, Sb, Cs, Ba, La, Ce, Sm, Tb, Yb, Hf, Ta, W, Au, Th, U) in mosses were determined by epithermal neutron activation analysis. The elem...

NKS NordRisk II: Atlas of long-range atmospheric dispersion and deposition of radionuclides from selected risk sites in the Northern Hemisphere

International Nuclear Information System (INIS)

Smith Korsholm, U.; Havskov Soerensen, J.; Astrup, P.; Lauritzen, B.

2011-04-01

The present atlas has been developed within the NKS/NordRisk-II project 'Nuclear risk from atmospheric dispersion in Northern Europe'. The atlas describes risks from hypothetical long-range dispersion and deposition of radionuclides from 16 nuclear risk sites on the Northern Hemisphere. The atmospheric dispersion model calculations cover a period of 30 days following each release to ensure almost complete deposition of the dispersed material. The atlas contains maps showing the total deposition and time-integrated air concentration of Cs-137 and I-131 based on three years of meteorological data spanning the climate variability associated with the North Atlantic Oscillation, and corresponding time evolution of the ensemble mean atmospheric dispersion. (Author)

NKS NordRisk II: Atlas of long-range atmospheric dispersion and deposition of radionuclides from selected risk sites in the Northern Hemisphere

Energy Technology Data Exchange (ETDEWEB)

Smith Korsholm, U.; Havskov Soerensen, J. (Danish Meteorological Institute (DMI), Copenhagen (Denmark)); Astrup, P.; Lauritzen, B. (Technical Univ. of Denmark, Risoe National Lab. for Sustainable Energy. Radiation Research Div., Roskilde (Denmark))

2011-04-15

The present atlas has been developed within the NKS/NordRisk-II project 'Nuclear risk from atmospheric dispersion in Northern Europe'. The atlas describes risks from hypothetical long-range dispersion and deposition of radionuclides from 16 nuclear risk sites on the Northern Hemisphere. The atmospheric dispersion model calculations cover a period of 30 days following each release to ensure almost complete deposition of the dispersed material. The atlas contains maps showing the total deposition and time-integrated air concentration of Cs-137 and I-131 based on three years of meteorological data spanning the climate variability associated with the North Atlantic Oscillation, and corresponding time evolution of the ensemble mean atmospheric dispersion. (Author)

Current state and temporal evolution of the chemical composition of atmospheric depositions in forest areas of the CONECOFOR network

Directory of Open Access Journals (Sweden)

Marchetto A

2014-04-01

Full Text Available Current state and temporal evolution of the chemical composition of atmospheric depositions in forest areas of the CONECOFOR network. Since 1997, atmospheric deposition was sampled and analyzed in the permanent plots of the Italian network for the evaluation of forest health (CONECOFOR, under the coordination of the Italian Forest Service. This paper presents the results of the activity carried out in 2009, when the EU-funded LIFE+ “FutMon” project allowed to extend the sampling network to 22 sites. Long-term trends will also be evaluated for the sampling sites with the longest time series. The sampling of open field bulk deposition was performed in a clearance close to the CONECOFOR permanent plots, while throughfall deposition and stemflow (in beech stand, only were sampled in the plot. Deposition samples were collected weekly and sent to the laboratories, where they were analyzed for pH, conductivity, major ions, and total carbon and nitrogen. Most measured variables showed a strong geographical gradient. For example, nitrogen deposition was relatively high in the Po plain (where the emissions of nitrogen oxides and ammonia are the highest and surrounding hills, reaching 10-20 kgN ha-1 y-1 in the open field and 13-25 kgN ha-1 y-1 in the throughfall. Sulphate deposition also showed a marked geographical gradient. Deposition of marine aerosol also had an important impact on the chemical composition of atmospheric deposition in Italy, together with the episodic deposition of Saharan dust, which showed a marked gradient, with highest values in the southernmost plots. Trend analysis was carried out on 10 sites running since the beginning of the program. A general negative trend in sulphate concentration was detected, paralleled in most plots by a positive trend in deposition pH, in good agreement with the strong reduction in the emission of sulphur dioxide recorded in the last decades. Nitrogen concentration also showed a significant decrease

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.

Deposition of radionuclides and their subsequent relocation in the environment following an accidental release to the atmosphere

International Nuclear Information System (INIS)

Underwood, B.Y.; Roed, J.; Paretzke, H.G.

1993-01-01

The objective of the project is to improve, as necessary, the models and parameterizations used in estimating the intensity and spatial distribution of deposited activity, and the total health/economic impact of such deposits in assessments of the consequences of accidental releases of radioactivity. The study comprises the influence of various weather conditions on deposition; the resuspension of deposited 137 Cs activity; the weathering of deposits in urban and rural environments; the ultimate fate and dosimetric impact of radionuclides carried by urban run-off water; the impact of the atmosphere's dispersion capabilities. Objectives and results of the four contributions to the project for the reporting period are presented. (R.P.) 5 refs., 4 figs., 1 tab

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

Science.gov (United States)

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

2016-09-19

-stage arrangement. With the modified IEC design, ammonium, nitrate, and sulfate ions were determined with a precision of between 5 and 10 percent relative standard deviation for the low loads that happen in remote areas of Alaska. Results from 2012 field studies demonstrated that the targeted ions were stable and fully retained on the IEC during field deployment and could be fully recovered by extraction in the laboratory. Importantly, measurements of annual loads determined by combining snowpack and IEC sampling at sites near National Atmospheric Deposition Program monitoring stations was comparable to results obtained by the National Atmospheric Deposition Program.Field studies completed in 2014 included snowpack and IEC samples to measure depositional loads; the results were compared to concentrations of similar substances in co-located moss samples. Analyses of constituents in snow and IECs included ammonium, nitrate, and sulfate ions; and a suite of trace metals. Constituent measurements in Hylocomium splendens moss included total nitrogen, phosphorous, and sulfur, and trace metals. To recover ammonium ions and metal ions from the upper cation-exchange column, a two-step extraction procedure was developed from laboratory spiking experiments. The 2014 studies determined that concentrations of certain metals, nitrogen, and sulfur in tissues of Hylocomium splendens moss reflected differences in presumptive deposition from local atmospheric sources. Moss tissues collected from two sites farthest from urban locales had the lowest levels of total nitrogen and sulfur, whereas tissues collected from three of the urban sites had the greatest concentrations of many of the trace metals. Moss tissue concentrations of three trace metals (cobalt, chromium, and nickel) were strongly (positively) Spearman’s rank correlated (presearch documents how the methodology can be used for future monitoring efforts in remote regions of Alaska and elsewhere.

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

Bioaccumulation behaviour of transplants of the lichen Flavoparmelia caperata in relation to total deposition at a polluted location in Portugal

International Nuclear Information System (INIS)

Godinho, R.M.; Wolterbeek, H.Th.; Verburg, T.; Freitas, M.C.

2008-01-01

This experiment compares the short and long time element accumulation behaviour of transplants of Flavoparmelia caperata lichen thalli and total deposition in an atmospheric polluted area. It was found that lichens exposed for a short time behaved differently from lichens in cumulative exposition suggesting the presence of acclimatization behaviour. The lichen transplant elemental content does not unequivocally represent the average or cumulative environmental availability of the exposure period. Reflection characteristics depend on the element and the lichen physiological conditions. Good correlations between lichen elemental contents and total deposition were obtained when a physiological lichen parameter was introduced in a mathematical model, suggesting that metabolically mediated accumulation is important. - The length of the foregoing atmospheric availability period reflected by lichen elemental contents is element-specific and depends on lichen physiological conditions

Depositional characteristics of atmospheric polybrominated diphenyl ethers on tree barks

Directory of Open Access Journals (Sweden)

Man Young Chun

2014-07-01

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

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

Science.gov (United States)

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

2014-01-01

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

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.

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...

Heavy metal atmospheric deposition study in the South Ural Mountains

International Nuclear Information System (INIS)

Frontasyeva, M.V.; Smirnov, L.I.; Lyapunov, S.M.

2004-01-01

Samples of the mosses Hylocomium splendens and Pleurozium schreberi, collected in the summer of 1998, were used to study the atmospheric deposition of heavy metals and other toxic elements in the Chelyabinsk Region situated in the South Urals, one of the most heavily polluted industrial areas of the Russian Federation. Samples of natural soils were collected simultaneously with moss at the same 30 sites in order to investigate surface accumulation of heavy metals and to examine the correlation of elements in moss and soil samples in order to separate contributions from atmospheric deposition and from soil minerals. A total of 38 elements (Na, Mg, Al, K, Ca, Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Zn, As, Se, Rb, Sr, Zr, Mo, Sb, Cs, Ba, La, Ce, Nd, Sm, Eu, Gd, Tb, Dy, Yb, Hf, Ta, W, Au, Th, U) in soil and 33 elements Na, Mg, Al, Cl, K, Ca, Sc, V, Cr, Mn, Fe, Co, Ni, Zn, As, Se, Br, Rb, Ag, Sb, Cs, Ba, La, Ce, Sm, Tb, Yb, Hf, Ta, W, Au, Th, U) were determined by epithermal neutron activation analysis. The elements Cu, Cd and Pb (in moss samples only) were obtained by atomic absorption spectrometry. VARIMAX rotated principal component analysis was used to identify and characterize different pollution sources and to point out the most polluted areas. (author)

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.

Mobility and contamination assessment of mercury in coal fly ash, atmospheric deposition, and soil collected from Tianjin, China.

Science.gov (United States)

Wei, Zheng; Wu, Guanghong; Su, Ruixian; Li, Congwei; Liang, Peiyu

2011-09-01

Samples of class F coal fly ash (levels I, II, and III), slag, coal, atmospheric deposition, and soils collected from Tianjin, China, were analyzed using U.S. Environmental Protection Agency (U.S. EPA) Method 3052 and a sequential extraction procedure, to investigate the pollution status and mobility of Hg. The results showed that total mercury (HgT) concentrations were higher in level I fly ash (0.304 µg/g) than in level II and level III fly ash and slag (0.142, 0.147, and 0.052 µg/g, respectively). Total Hg in the atmospheric deposition was higher during the heating season (0.264 µg/g) than the nonheating season (0.135 µg/g). Total Hg contents were higher in suburban area soils than in rural and agricultural areas. High HgT concentrations in suburban area soils may be a result of the deposition of Hg associated with particles emitted from coal-fired power plants. Mercury in fly ash primarily existed as elemental Hg, which accounted for 90.1, 85.3, and 90.6% of HgT in levels I, II, and III fly ash, respectively. Mercury in the deposition existed primarily as sulfide Hg, which accounted for 73.8% (heating season) and 74.1% (nonheating season) of HgT. However, Hg in soils existed primarily as sulfide Hg, organo-chelated Hg and elemental Hg, which accounted for 37.8 to 50.0%, 31.7 to 41.8%, and 13.0 to 23.9% of HgT, respectively. The percentage of elemental Hg in HgT occurred in the order fly ash > atmospheric deposition > soils, whereas organo-chelated Hg and sulfide Hg occurred in the opposite order. The present approach can provide a window for understanding and tracing the source of Hg in the environment in Tianjin and the risk associated with Hg bioaccessibility. Copyright © 2011 SETAC.

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

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,...

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

Energy Technology Data Exchange (ETDEWEB)

Azimi, S

2004-07-15

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

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

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.

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 Influence of Climate Change on Atmospheric Deposition of Mercury in the Arctic—A Model Sensitivity Study

Science.gov (United States)

Hansen, Kaj M.; Christensen, Jesper H.; Brandt, Jørgen

2015-01-01

Mercury (Hg) is a global pollutant with adverse health effects on humans and wildlife. It is of special concern in the Arctic due to accumulation in the food web and exposure of the Arctic population through a rich marine diet. Climate change may alter the exposure of the Arctic population to Hg. We have investigated the effect of climate change on the atmospheric Hg transport to and deposition within the Arctic by making a sensitivity study of how the atmospheric chemistry-transport model Danish Eulerian Hemispheric Model (DEHM) reacts to climate change forcing. The total deposition of Hg to the Arctic is 18% lower in the 2090s compared to the 1990s under the applied Special Report on Emissions Scenarios (SRES-A1B) climate scenario. Asia is the major anthropogenic source area (25% of the deposition to the Arctic) followed by Europe (6%) and North America (5%), with the rest arising from the background concentration, and this is independent of the climate. DEHM predicts between a 6% increase (Status Quo scenario) and a 37% decrease (zero anthropogenic emissions scenario) in Hg deposition to the Arctic depending on the applied emission scenario, while the combined effect of future climate and emission changes results in up to 47% lower Hg deposition. PMID:26378551

Atmospheric nitrogen deposition influences denitrification and nitrous oxide production in lakes.

Science.gov (United States)

McCrackin, Michelle L; Elser, James J

2010-02-01

Microbially mediated denitrification is an important process that may ameliorate the effects of nitrogen (N) loading by permanently removing excess N inputs. In this study, we measured the rate of denitrification and nitrous oxide (N2O) production during denitrification in sediments from 32 Norwegian lakes at the high and low ends of a gradient of atmospheric N deposition. Denitrification and N2O production rates averaged 41.7 and 1.1 micromol N x m(-2) x h(-1), respectively, for high-deposition lakes. There was no detectable denitrification or N2O production in low-deposition lakes. Epilimnetic nitrate concentration was strongly correlated with denitrification rate (r2 = 0.67). We also measured the denitrification rate in response to experimental additions of organic carbon, nitrate, and phosphorus. Experimental nitrate additions stimulated denitrification in sediments of all lakes, regardless of N deposition level. In fact, the rate of denitrification in nitrate-amended treatments was the same magnitude for lakes in both deposition areas. These findings suggest that lake sediments possess considerable capacity to remove nitrate and that this capacity has not been saturated under conditions of chronic N loading. Further, nitrous oxide was nearly 3% of the total gaseous product during denitrification in high-deposition lakes, a fraction that is comparable to polluted marine sediments. Our findings suggest that, while lakes play an important role in N removal in the landscape, they may be a source of N2O emissions, especially in areas subject to elevated N inputs.

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

Directory of Open Access Journals (Sweden)

M. Amodio

2014-01-01

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

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...

Tracing the fate of atmospheric nitrate deposited onto a forest ecosystem in Eastern Asia using Δ17O

Directory of Open Access Journals (Sweden)

I. Noguchi

2010-02-01

Full Text Available The stable isotopic compositions of nitrate in precipitation (wet deposition and groundwater (spring, lake, and stream water were determined for the island of Rishiri, Japan, so as to use the 17O anomalies (Δ17O to trace the fate of atmospheric nitrate that had deposited onto the island ecosystem, which is a representative background forest ecosystem for eastern Asia. The deposited nitrate had large 17O anomalies with Δ17O values ranging from +20.8‰ to +34.5‰ (n = 32 with +26.2‰ being the annual average. The maximum Δ17O value of +34.5‰, obtained for precipitation on the 23rd to 24th of February 2007, was an extraordinarily large value among values for all samples of precipitation in Rishiri. Most nitrate in the sample might have been produced via NO3 radical in a highly polluted air mass that had been supplied from megacities on the eastern coast of the Asian continent. On the other hand, nitrate in groundwater had small Δ17O values ranging from +0.9‰ to 3.2‰ (n = 19, which corresponds to an mixing ratio of atmospheric nitrate to total nitrate of (7.4±2.6%. Comparing the inflow and outflow of atmospheric nitrate in groundwater within the island, we estimated that the direct drainage accounts for (8.8±4.6% of atmospheric nitrate that has deposited on the island and that the residual portion has undergone biological processing before being exported from the forest ecosystem.

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

International Nuclear Information System (INIS)

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

2002-01-01

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

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)

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.

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 ammonia measurements along the coastal lines of Southeastern China: Implications for inorganic nitrogen deposition to coastal waters

Science.gov (United States)

Wu, Shui-Ping; Dai, Lu-Hong; Wei, Ya; Zhu, Heng; Zhang, Yin-Ju; Schwab, James J.; Yuan, Chung-Shin

2018-03-01

Ambient NH3 concentrations were determined using Ogawa passive samplers along the coastal lines of southeast China from June 2015 to May 2017. Additional monitoring of PM2.5 and precipitation around Xiamen Bay during the period from November 2015 to May 2017 were carried out to estimate atmospheric inorganic nitrogen (IN) deposition to the bay. Distinct seasonal variations of ambient NH3 were observed with summer averages 1.41-5.56 times higher than winter, which agreed well with the seasonal trend of air temperature. Nitrate concentrations (pNO3-) in PM2.5 were significantly higher than ammonium concentrations (pNH4+), and both species showed higher concentrations in winter and spring and lower values in summer and fall which were influenced mainly by the monsoon cycle, gas-to-particle transformation process and rain washout. Paired t-testing revealed that no significant differences of pNO3- and pNH4+ between the urban and suburban sites around the Xiamen Bay. Unlike pNO3- and pNH4+, there were no clear seasonal trends for NH4+ and NO3- concentrations in precipitation samples (wNH4+ and wNO3-). On average, the deposition of IN consisted of NH3-N (27.4-28.2%) and pNO3--N (25.9-26.8%), followed by pNH4+-N (17.0-17.7%), wNH4+-N (14.5%), wNO3--N (13.3-13.8%) and NO2-N (0.35-0.46%); and showed distinct seasonal trends with higher values in winter/spring and lower values in summer/fall. In 2016, the total IN deposition was determined to be 36.45 and 35.92 kg N ha-1 at the urban and suburban sites around the Xiamen Bay, respectively. The proportion of IN deposition to total IN loads (terrestrial + atmospheric), varied over the range of 7.1-13.3% depending on the data source of riverine influx. Our observations revealed that the total IN deposition could account for 9.6-25.1% (based on primary productivity over Taiwan Strait) and 1.7-5.3% (based on primary productivity in Guangdong coastal region) of new productivity in Xiamen Bay, respectively. As an important nutrient

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.

Dispersion, deposition and resuspension of atmospheric contaminants

International Nuclear Information System (INIS)

Anon.

1985-01-01

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

Atmospheric aerosol in an urban area: Comparison of measurement instruments and methodologies and pulmonary deposition assessment

International Nuclear Information System (INIS)

Berico, M.; Luciani, A.; Formignani, M.

1996-07-01

In March 1995 a measurement campaign of atmospheric aerosol in the Bologna urban area (Italy) was carried out. A transportable laboratory, set up by ENEA (Italian national Agency for New Technologies, Energy and the Environment) Environmental Department (Bologna), was utilized with instruments for measurement of atmospheric aerosol and meteorological parameters. The aim of this campaign was of dual purpose: to characterize aerosol in urban area and to compare different instruments and methodologies of measurements. Mass concentrations measurements, evaluated on a 23-hour period with total filter, PM10 dichotomous sampler and low pressure impactor (LPI Berner), have provided information respectively about total suspended particles, respirable fraction and granulometric parameters of aerosol. Eight meteorologic parameters, number concentration of submicromic fraction of aerosol and mass concentration of micromic fraction have been continually measured. Then, in a daytime period, several number granulometries of atmospheric aerosol have also been estimated by means of diffusion battery system. Results related to different measurement methodologies and granulometric characteristics of aerosol are presented here. Pulmonary deposition of atmospheric aerosol is finally calculated, using granulometries provided by LPI Brener and ICRP 66 human respiratory tract model

A heavy metal atmospheric deposition study in the South Ural mountains

International Nuclear Information System (INIS)

Frontas'eva, M.V.; Smirnov, L.I.; Steinnes, E.; Lyapunov, S.M.; Cherchintsev, V.D.

2002-01-01

Samples of the mosses Hylocomium splendens and Pleurozium schreberi, collected in the summer of 1998, were used to study the atmospheric deposition of heavy metals and other toxic elements in the Chelyabinsk Region situated in the South Ural, one of the most heavily poluted industrial areas of the Russian Federation. Samples of natural soils were collected simultaneously with moss at the same 30 sites in order to investigate surface accumulation of heavy metals and to examine the correlation of elements in moss and soil samples in order to separate contributions from atmospheric deposition and from soil minerals. A total of 38 elements (Na, Mg, Al, K, Ca, Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Zn, As, Se, Rb, Sr, Zr, Mo, Sb, Cs, Ba, La, Ce, Nd, Sm, Eu, Gd, Tb, Dy, Yb, Hf, Tf, W, Au, Th, U) in soil and 33 elements (Na, Mg, Al, Cl, K, Ca, Sc, V, Cr, Mn, Fe, Co, Ni, Zn, As, Se, Br, Rb, Ag, Sb, Cs, Ba, La, Ce, Sm, Tb, Yb, Hf, Ta, W, Au, Th, U) in mosses were determined by epithermal neutron activation analysis, The elements Cu, Cd and Pb (in moss samples only) were obtained by atomic absorption spectrometry. The element concentrations were compared to those for copper basins in Poland and Serbia as well as to baseline concentrations in Norway. VARIMAX rotated principal component analysis was used to identify and characterise different pollution sources and to point out the most polluted areas

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....

External quality-assurance project report for the National Atmospheric Deposition Program/National Trends Network and Mercury Deposition Network, 2009-2010

Science.gov (United States)

Wetherbee, Gregory A.; Martin, RoseAnn; Rhodes, Mark F.; Chesney, Tanya A.

2014-01-01

The U.S. Geological Survey operated six distinct programs to provide external quality-assurance monitoring for the National Atmospheric Deposition Program/National Trends Network (NTN) and Mercury Deposition Network (MDN) during 2009–2010. The field-audit program assessed the effects of onsite exposure, sample handling, and shipping on the chemistry of NTN samples; a system-blank program assessed the same effects for MDN. Two interlaboratory-comparison programs assessed the bias and variability of the chemical analysis data from the Central Analytical Laboratory (CAL) and Mercury (Hg) Analytical Laboratory (HAL). The blind-audit program was also implemented for the MDN to evaluate analytical bias in total Hg concentration data produced by the HAL. The co-located-sampler program was used to identify and quantify potential shifts in NADP data resulting from replacement of original network instrumentation with new electronic recording rain gages (E-gages) and precipitation collectors that use optical sensors. The results indicate that NADP data continue to be of sufficient quality for the analysis of spatial distributions and time trends of chemical constituents in wet deposition across the United States. Results also suggest that retrofit of the NADP networks with the new precipitation collectors could cause –8 to +14 percent shifts in NADP annual precipitation-weighted mean concentrations and total deposition values for ammonium, nitrate, sulfate, and hydrogen ion, and larger shifts (+13 to +74 percent) for calcium, magnesium, sodium, potassium, and chloride. The prototype N-CON Systems bucket collector is more efficient in the catch of precipitation in winter than Aerochem Metrics Model 301 collector, especially for light snowfall.

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

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

Science.gov (United States)

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

2016-03-01

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

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

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

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

Xenon-133 and caesium-137 releases into the atmosphere from the Fukushima Dai-ichi nuclear power plant: determination of the source term, atmospheric dispersion, and deposition

Science.gov (United States)

Stohl, A.; Seibert, P.; Wotawa, G.; Arnold, D.; Burkhart, J. F.; Eckhardt, S.; Tapia, C.; Vargas, A.; Yasunari, T. J.

2012-04-01

This presentation will show the results of a paper currently under review in ACPD and some additional new results, including more data and with an independent box modeling approach to support some of the findings of the ACPD paper. On 11 March 2011, an earthquake occurred about 130 km off the Pacific coast of Japan's main island Honshu, followed by a large tsunami. The resulting loss of electric power at the Fukushima Dai-ichi nuclear power plant (FD-NPP) developed into a disaster causing massive release of radioactivity into the atmosphere. In this study, we determine the emissions of two isotopes, the noble gas xenon-133 (133Xe) and the aerosol-bound caesium-137 (137Cs), which have very different release characteristics as well as behavior in the atmosphere. To determine radionuclide emissions as a function of height and time until 20 April, we made a first guess of release rates based on fuel inventories and documented accident events at the site. This first guess was subsequently improved by inverse modeling, which combined the first guess with the results of an atmospheric transport model, FLEXPART, and measurement data from several dozen stations in Japan, North America and other regions. We used both atmospheric activity concentration measurements as well as, for 137Cs, measurements of bulk deposition. Regarding 133Xe, we find a total release of 16.7 (uncertainty range 13.4-20.0) EBq, which is the largest radioactive noble gas release in history not associated with nuclear bomb testing. There is strong evidence that the first strong 133Xe release started early, before active venting was performed. The entire noble gas inventory of reactor units 1-3 was set free into the atmosphere between 11 and 15 March 2011. For 137Cs, the inversion results give a total emission of 35.8 (23.3-50.1) PBq, or about 42% of the estimated Chernobyl emission. Our results indicate that 137Cs emissions peaked on 14-15 March but were generally high from 12 until 19 March, when they

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

A Hybrid Approach for Estimating Total Deposition in the United States

Science.gov (United States)

Atmospheric deposition of nitrogen and sulfur causes many deleterious effects on ecosystems including acidification and excess eutrophication. Assessments to support development of strategies to mitigate these effects require spatially and temporally continuous values of nitrogen...

Meridional transport and deposition of atmospheric 10Be

Directory of Open Access Journals (Sweden)

J. Feichter

2009-01-01

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

A 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.

Comparison of annual dry and wet deposition fluxes of selected pesticides in Strasbourg, France

International Nuclear Information System (INIS)

Sauret, Nathalie; Wortham, Henri; Strekowski, Rafal; Herckes, Pierre; Nieto, Laura Ines

2009-01-01

This work summarizes the results of a study of atmospheric wet and dry deposition fluxes of Deisopropyl-atrazine (DEA), Desethyl-atrazine (DET), Atrazine, Terbuthylazine, Alachlor, Metolachlor, Diflufenican, Fenoxaprop-p-ethyl, Iprodione, Isoproturon and Cymoxanil pesticides conducted in Strasbourg, France, from August 2000 through August 2001. The primary objective of this work was to calculate the total atmospheric pesticide deposition fluxes induced by atmospheric particles. To do this, a modified one-dimensional cloud water deposition model was used. All precipitation and deposition samples were collected at an urban forested park environment setting away from any direct point pesticide sources. The obtained deposition fluxes induced by atmospheric particles over a forested area showed that the dry deposition flux strongly contributes to the total deposition flux. The dry particle deposition fluxes are shown to contribute from 4% (DET) to 60% (cymoxanil) to the total deposition flux (wet + dry). - A modified one-dimensional cloud water deposition model is used to estimate the deposition fluxes of pesticides in the particle phase and compare the relative importance of dry and wet depositions

Comparison of annual dry and wet deposition fluxes of selected pesticides in Strasbourg, France

Energy Technology Data Exchange (ETDEWEB)

Sauret, Nathalie [Marseilles University, Laboratoire Chimie Provence - UMR 6264, Campus Saint Charles, Case 29, 3 Place Victor Hugo, 13331 Marseilles Cedex 03 (France); Wortham, Henri [Marseilles University, Laboratoire Chimie Provence - UMR 6264, Campus Saint Charles, Case 29, 3 Place Victor Hugo, 13331 Marseilles Cedex 03 (France)], E-mail: Henri.Wortham@univ-provence.fr; Strekowski, Rafal [Marseilles University, Laboratoire Chimie Provence - UMR 6264, Campus Saint Charles, Case 29, 3 Place Victor Hugo, 13331 Marseilles Cedex 03 (France); Herckes, Pierre [Arizona State University, Department of Chemistry and Biochemistry, Tempe, AZ 85287-1604 (United States); Nieto, Laura Ines [Marseilles University, Laboratoire Chimie Provence - UMR 6264, Campus Saint Charles, Case 29, 3 Place Victor Hugo, 13331 Marseilles Cedex 03 (France)

2009-01-15

This work summarizes the results of a study of atmospheric wet and dry deposition fluxes of Deisopropyl-atrazine (DEA), Desethyl-atrazine (DET), Atrazine, Terbuthylazine, Alachlor, Metolachlor, Diflufenican, Fenoxaprop-p-ethyl, Iprodione, Isoproturon and Cymoxanil pesticides conducted in Strasbourg, France, from August 2000 through August 2001. The primary objective of this work was to calculate the total atmospheric pesticide deposition fluxes induced by atmospheric particles. To do this, a modified one-dimensional cloud water deposition model was used. All precipitation and deposition samples were collected at an urban forested park environment setting away from any direct point pesticide sources. The obtained deposition fluxes induced by atmospheric particles over a forested area showed that the dry deposition flux strongly contributes to the total deposition flux. The dry particle deposition fluxes are shown to contribute from 4% (DET) to 60% (cymoxanil) to the total deposition flux (wet + dry). - A modified one-dimensional cloud water deposition model is used to estimate the deposition fluxes of pesticides in the particle phase and compare the relative importance of dry and wet depositions.

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

Science.gov (United States)

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

2009-01-01

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

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.

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 .

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

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

International Nuclear Information System (INIS)

Singh, Raj Kumar; Agrawal, Madhoolika

2005-01-01

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

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

Science.gov (United States)

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

2013-12-01

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

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.

[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 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

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

Science.gov (United States)

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

2014-06-01

release rates associated with reactor pressure changes in Units 2 and 3. The modified WSPEEDI-II simulation using the new source term reproduced local and regional patterns of cumulative surface deposition of total 131I and 137Cs and air dose rate obtained by airborne surveys. The new source term was also tested using three atmospheric dispersion models (MLDP0, HYSPLIT, and NAME) for regional and global calculations and showed good agreement between calculated and observed air concentration and surface deposition of 137Cs in East Japan. Moreover, HYSPLIT model using the new source term also reproduced the plume arrivals at several countries abroad showing a good correlation with measured air concentration data. A large part of deposition pattern of total 131I and 137Cs in East Japan was explained by in-cloud particulate scavenging. However, for the regional scale contaminated areas, there were large uncertainties due to the overestimation of rainfall amounts and the underestimation of fogwater and drizzle depositions. The computations showed that approximately 27% of 137Cs discharged from FNPS1 deposited to the land in East Japan, mostly in forest areas.

Xenon-133 and caesium-137 releases into the atmosphere from the Fukushima Dai-ichi nuclear power plant: determination of the source term, atmospheric dispersion, and deposition

Directory of Open Access Journals (Sweden)

A. Stohl

2012-03-01

Full Text Available On 11 March 2011, an earthquake occurred about 130 km off the Pacific coast of Japan's main island Honshu, followed by a large tsunami. The resulting loss of electric power at the Fukushima Dai-ichi nuclear power plant developed into a disaster causing massive release of radioactivity into the atmosphere. In this study, we determine the emissions into the atmosphere of two isotopes, the noble gas xenon-133 (¹³³Xe and the aerosol-bound caesium-137 (¹³⁷Cs, which have very different release characteristics as well as behavior in the atmosphere. To determine radionuclide emissions as a function of height and time until 20 April, we made a first guess of release rates based on fuel inventories and documented accident events at the site. This first guess was subsequently improved by inverse modeling, which combined it with the results of an atmospheric transport model, FLEXPART, and measurement data from several dozen stations in Japan, North America and other regions. We used both atmospheric activity concentration measurements as well as, for ¹³⁷Cs, measurements of bulk deposition. Regarding ¹³³Xe, we find a total release of 15.3 (uncertainty range 12.2–18.3 EBq, which is more than twice as high as the total release from Chernobyl and likely the largest radioactive noble gas release in history. The entire noble gas inventory of reactor units 1–3 was set free into the atmosphere between 11 and 15 March 2011. In fact, our release estimate is higher than the entire estimated ¹³³Xe inventory of the Fukushima Dai-ichi nuclear power plant, which we explain with the decay of iodine-133 (half-life of 20.8 h into ¹³³Xe. There is strong evidence that the ¹³³Xe release started before the first active venting was made, possibly indicating structural damage to reactor components and/or leaks due to overpressure which would have allowed early release of noble gases. For ¹³⁷

Xenon-133 and caesium-137 releases into the atmosphere from the Fukushima Dai-ichi nuclear power plant. Determination of the source term, atmospheric dispersion, and deposition

International Nuclear Information System (INIS)

Stohl, A.; Burkhart, J.F.; Eckhardt, S.; Seibert, P.; Arnold, D.; Technical Univ. of Catalonia, Barcelona; Tapia, C.; Vargas, A.; Yasunari, T.J.

2012-01-01

On 11 March 2011, an earthquake occurred about 130 km off the Pacific coast of Japan's main island Honshu, followed by a large tsunami. The resulting loss of electric power at the Fukushima Dai-ichi nuclear power plant developed into a disaster causing massive release of radioactivity into the atmosphere. In this study, we determine the emissions into the atmosphere of two isotopes, the noble gas xenon-133 ("1"3"3Xe) and the aerosol-bound caesium-137 ("1"3"7Cs), which have very different release characteristics as well as behavior in the atmosphere. To determine radionuclide emissions as a function of height and time until 20 April, we made a first guess of release rates based on fuel inventories and documented accident events at the site. This first guess was subsequently improved by inverse modeling, which combined it with the results of an atmospheric transport model, FLEXPART, and measurement data from several dozen stations in Japan, North America and other regions. We used both atmospheric activity concentration measurements as well as, for "1"3"7Cs, measurements of bulk deposition. Regarding "1"3"3Xe, we find a total release of 15.3 (uncertainty range 12.2-18.3) EBq, which is more than twice as high as the total release from Chernobyl and likely the largest radioactive noble gas release in history. The entire noble gas inventory of reactor units 1-3 was set free into the atmosphere between 11 and 15 March 2011. In fact, our release estimate is higher than the entire estimated "1"3"3Xe inventory of the Fukushima Dai-ichi nuclear power plant, which we explain with the decay of iodine-133 (half-life of 20.8 h) into "1"3"3Xe. There is strong evidence that the "1"3"3Xe release started before the first active venting was made, possibly indicating structural damage to reactor components and/or leaks due to overpressure which would have allowed early release of noble gases. For "1"3"7Cs, the inversion results give a total emission of 36.6 (20.1-53.1) PBq, or about

Xenon-133 and caesium-137 releases into the atmosphere from the Fukushima Dai-ichi nuclear power plant. Determination of the source term, atmospheric dispersion, and deposition

Energy Technology Data Exchange (ETDEWEB)

Stohl, A.; Burkhart, J.F.; Eckhardt, S. [NILU - Norwegian Institute for Air Research, Kjeller (Norway); Seibert, P. [Univ. of Natural Resources and Life Sciences, Vienna (Austria). Inst. of Meteorology; Wotawa, G. [Central Institute for Meteorology and Geodynamics, Vienna (Austria); Arnold, D. [Univ. of Natural Resources and Life Sciences, Vienna (Austria). Inst. of Meteorology; Technical Univ. of Catalonia, Barcelona (Spain). Inst. of Energy Technologies; Tapia, C. [Technical Univ. of Catalonia, Barcelona (Spain). Dept. of Physics and Nucelar Engineering; Vargas, A. [Technical Univ. of Catalonia, Barcelona (Spain). Inst. of Energy Technologies; Yasunari, T.J. [Univs. Space Research Association, Columbia, MD (United States). Goddard Earth Sciences and Technology and Research

2012-07-01

On 11 March 2011, an earthquake occurred about 130 km off the Pacific coast of Japan's main island Honshu, followed by a large tsunami. The resulting loss of electric power at the Fukushima Dai-ichi nuclear power plant developed into a disaster causing massive release of radioactivity into the atmosphere. In this study, we determine the emissions into the atmosphere of two isotopes, the noble gas xenon-133 ({sup 133}Xe) and the aerosol-bound caesium-137 ({sup 137}Cs), which have very different release characteristics as well as behavior in the atmosphere. To determine radionuclide emissions as a function of height and time until 20 April, we made a first guess of release rates based on fuel inventories and documented accident events at the site. This first guess was subsequently improved by inverse modeling, which combined it with the results of an atmospheric transport model, FLEXPART, and measurement data from several dozen stations in Japan, North America and other regions. We used both atmospheric activity concentration measurements as well as, for {sup 137}Cs, measurements of bulk deposition. Regarding {sup 133}Xe, we find a total release of 15.3 (uncertainty range 12.2-18.3) EBq, which is more than twice as high as the total release from Chernobyl and likely the largest radioactive noble gas release in history. The entire noble gas inventory of reactor units 1-3 was set free into the atmosphere between 11 and 15 March 2011. In fact, our release estimate is higher than the entire estimated {sup 133}Xe inventory of the Fukushima Dai-ichi nuclear power plant, which we explain with the decay of iodine-133 (half-life of 20.8 h) into {sup 133}Xe. There is strong evidence that the {sup 133}Xe release started before the first active venting was made, possibly indicating structural damage to reactor components and/or leaks due to overpressure which would have allowed early release of noble gases. For {sup 137}Cs, the inversion results give a total emission of 36

A Novel Hybrid Approach for Estimating Total Deposition in the United States

Science.gov (United States)

Atmospheric deposition of nitrogen and sulfur causes many deleterious effects on ecosystems including acidification and excess eutrophication. Assessments to support development of strategies to mitigate these effects require spatially and temporally continuous values of nitrogen...

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)

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

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.

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

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

Energy Technology Data Exchange (ETDEWEB)

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

2015-07-01

cumulative surface deposition of total {sup 131}I and {sup 137}Cs and air dose rate obtained by airborne surveys. The new source term was also tested using three atmospheric dispersion models (Modele Lagrangien de Dispersion de Particules d'ordre zero: MLDP0, Hybrid Single Particle Lagrangian Integrated Trajectory Model: HYSPLIT, and Met Office's Numerical Atmospheric-dispersion Modelling Environment: NAME) for regional and global calculations, and the calculated results showed good agreement with observed air concentration and surface deposition of {sup 137}Cs in eastern Japan.

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

Directory of Open Access Journals (Sweden)

X. W. Fu

2010-03-01

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

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

International Nuclear Information System (INIS)

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

2011-01-01

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

Ammonia volatilization and atmospheric N deposition following straw and urea application from a rice-wheat rotation in southeastern China

Science.gov (United States)

Sun, Liying; Wu, Zhen; Ma, Yuchun; Liu, Yinglie; Xiong, Zhengqin

2018-05-01

Ammonia is a vital component of the nitrogen (N) cycle of terrestrial ecosystems in terms of volatilization and deposition. Here, a field experiment was undertaken to simultaneously investigate the effects of rice straw and urea incorporation on ammonia volatilization, atmospheric N deposition, yields and agronomic nitrogen use efficiency (NUE) under a rice-wheat system in China. The experiment involved four treatments: control (0 N, 0 straw), NS0 (250 kg N ha-1 season-1, 0 straw), NS1 (250 kg N ha-1 season-1, 3 t ha-1 yr-1 straw), and NS2 (250 kg N ha-1 season-1, 6 t ha-1 yr-1 straw) in the rice-wheat annual rotation system. The results indicated that the NS0, NS1 and NS2 treatments emitted cumulative ammonia of 14.0%, 16.4%, and 19.2%, respectively in the rice season and 7.6%, 11.1%, and 12.3%, respectively in the wheat season among the total urea-N application. Compared to the NS0 treatment, the NS1 and NS2 treatments significantly increased the cumulative ammonia emissions by 15.5% (p NH4+-N deposition accounted for 56.1% of the total inorganic N deposition during the whole rice-wheat system. The bulk NH4+-N deposition during the period of fertilization contributed 73.9% and 5.7% to the total NH4+-N deposition in the rice and wheat season, respectively. Overall, straw incorporation increased ammonia volatilization, not affecting the crop grain yield or NUE. The seasonal variation in NH4+-N bulk deposition was closely related to N fertilizer application.

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)

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.

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

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.

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

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

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

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)

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

Science.gov (United States)

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

2017-07-01

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

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

Science.gov (United States)

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

2013-12-01

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

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

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...

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

Science.gov (United States)

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

2009-01-01

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

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.

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.

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)

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

Science.gov (United States)

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. Copyright © 2017. Published by Elsevier Ltd.

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

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

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.

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

Directory of Open Access Journals (Sweden)

Stuart J. Piketh

2011-03-01

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

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

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

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

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

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

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)

NKS NordRisk. Atlas of long-range atmospheric dispersion and deposition of radionuclides from selected risk sites in the Northern Hemisphere

International Nuclear Information System (INIS)

Havskov Soerensen, J.; Baklanov, A.; Mahura, A.; Lauritzen, Bent; Mikkelsen, Torben

2008-07-01

Within the NKS NordRisk project, 'Nuclear risk from atmospheric dispersion in Northern Europe', the NKS NordRisk Atlas has been developed. The atlas describes risks from hypothetical long-range atmospheric dispersion and deposition of radionuclides from selected nuclear risk sites in the Northern Hemisphere. A number of case studies of long-term long-range atmospheric transport and deposition of radionuclides has been developed, based on two years of meteorological data. Radionuclide concentrations in air and radionuclide depositions have been evaluated and examples of long-term averages of the dispersion and deposition and of the variability around these mean values are provided. (au)

Impacts of atmospheric nitrogen deposition on vegetation and soils in Joshua Tree National Park

Science.gov (United States)

E.B. Allen; L. Rao; R.J. Steers; A. Bytnerowicz; M.E. Fenn

2009-01-01

The western Mojave Desert is downwind of nitrogen emissions from coastal and inland urban sources, especially automobiles. The objectives of this research were to measure reactive nitrogen (N) in the atmosphere and soils along a N-deposition gradient at Joshua Tree National Park and to examine its effects on invasive and native plant species. Atmospheric nitric acid (...

Indirect N2O emission due to atmospheric N deposition for the Netherlands

International Nuclear Information System (INIS)

Denier van der Gon, H.; Bleeker, A.

2005-10-01

Nitrous oxide (N2O) is a potent greenhouse gas produced in soils and aquatic systems. The UNFCCC requires participants to report 'indirect' N2O emissions, following from agricultural N losses to ground- and surface water and N deposition on (other) ecosystems due to agricultural sources. Indirect N2O emission due to atmospheric N deposition is presently not reported by the Netherlands. In this paper, we quantify the consequences of various tiers to estimate indirect N2O due to deposition for a country with a high agricultural N use and discuss the reliability and potential errors in the IPCC methodology. A literature review suggests that the current IPCC default emission factor for indirect N2O from N deposition is underestimated by a factor 2. Moreover, considering anthropogenic N emissions from agriculture only and not from e.g., traffic and industry, results in further underestimation of indirect N2O emissions. We calculated indirect N2O emissions due to Dutch anthropogenic N emissions to air by using official Dutch N emission data as input in an atmospheric transport and deposition model in combination with land use databases. Next, land use-specific emission factors were used to estimate the indirect N2O emission. This revealed that (1) for some countries, like the Netherlands, most agricultural N emitted will be deposited on agricultural soils, not on natural ecosystems and, (2) indirect N2O emissions are at least 20% higher because more specific emission factors can be applied that are higher than the IPCC default. The results suggest that indirect N2O emission due to deposition is underestimated in current N2O budgets

Modelling the impact of climate change and atmospheric N deposition on French forests biodiversity

International Nuclear Information System (INIS)

Rizzetto, Simon; Belyazid, Salim; Gégout, Jean-Claude; Nicolas, Manuel; Alard, Didier; Corcket, Emmanuel; Gaudio, Noémie; Sverdrup, Harald; Probst, Anne

2016-01-01

A dynamic coupled biogeochemical–ecological model was used to simulate the effects of nitrogen deposition and climate change on plant communities at three forest sites in France. The three sites had different forest covers (sessile oak, Norway spruce and silver fir), three nitrogen loads ranging from relatively low to high, different climatic regions and different soil types. Both the availability of vegetation time series and the environmental niches of the understory species allowed to evaluate the model for predicting the composition of the three plant communities. The calibration of the environmental niches was successful, with a model performance consistently reasonably high throughout the three sites. The model simulations of two climatic and two deposition scenarios showed that climate change may entirely compromise the eventual recovery from eutrophication of the simulated plant communities in response to the reductions in nitrogen deposition. The interplay between climate and deposition was strongly governed by site characteristics and histories in the long term, while forest management remained the main driver of change in the short term. - Highlights: • The effects of N atmospheric deposition and climate change on vegetation were simulated. • The model ForSAFE-Veg was calibrated and validated carefully for three forests in France. • Climate has a greater influence on vegetation than N deposition in conifer forests. • N-poor ecosystems are, however, more sensitive to N deposition than to climate change. - Compared to nitrogen atmospheric deposition, climate appears to be the main driver of change in forest plant biodiversity on a century scale, except in N-poor ecosystems.

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

Science.gov (United States)

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

2000-01-01

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

UFOMOD - atmospheric dispersion and deposition

International Nuclear Information System (INIS)

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

1989-10-01

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

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

Epiphytic lichens as quantitative biomonitors for atmospheric element deposition

International Nuclear Information System (INIS)

Jeran, Z.; Jacimovic, J.; Smodis, B.; Batic, F.

2000-01-01

Epiphytic lichens are being used as passive and active biomonitors of trace elements in Slovenia. The lichen Hypogymnia physodes (L.) Nyl. was exposed at three locations (two in the vicinity of a coal fired-power plant, and one at a reference location) for 8 months. At the same locations air particulate matter and total deposition were collected on a monthly basis. The k 0 -method of neutron activation analysis, using the TRIGA Mark II reactor at the 'Jozef Stefan' Institute, was employed for multielemental nondestructive analysis of all samples. The influence of the power plant on the concentration levels of some elements in the transplanted lichens, air particulates and total deposition is discussed and their correlation presented. (author)

Atmospheric deposition of inorganic nitrogen in Spanish forests of Quercus ilex measured with ion-exchange resins and conventional collectors

Science.gov (United States)

Héctor García-Gomez; Sheila Izquieta-Rojano; Laura Aguillaume; Ignacio González-Fernández; Fernando Valiño; David Elustondo; Jesús M. Santamaría; Anna Àvila; Mark E. Fenn; Rocío Alonso

2016-01-01

Atmospheric nitrogen deposition is one of the main threats for biodiversity and ecosystem functioning. Measurement techniques like ion-exchange resin collectors (IECs), which are less expensive and time-consuming than conventional methods, are gaining relevance in the study of atmospheric deposition and are recommended to expand monitoring networks. In the present work...

Oxygen in the Martian atmosphere: Regulation of PO2 by the deposition of iron formations on Mars

Science.gov (United States)

Burns, Roger G.

1992-01-01

During Earth's early history, and prior to the evolution of its present day oxygenated atmosphere, extensive iron rich siliceous sedimentary rocks were deposited, consisting of alternating layers of silica (chert) and iron oxide minerals (hematite and magnetite). The banding in iron formations recorded changes of atmosphere-hydrosphere interactions near sea level in the ancient ocean, which induced the oxidation of dissolved ferrous iron, precipitation of insoluble ferric oxides and silica, and regulation of oxygen in Earth's early atmosphere. Similarities between the Archean Earth and the composition of the present day atmosphere on Mars, together with the pervasive presence of ferric oxides in the Martian regolith suggest that iron formation might also have been deposited on Mars and influenced the oxygen content of the Martian atmosphere. Such a possibility is discussed here with a view to assessing whether the oxygen content of the Martian atmosphere has been regulated by the chemical precipitation of iron formations on Mars.

Temporal and spatial trends studied by lichen analysis: atmospheric deposition of trace elements in Mexico

Energy Technology Data Exchange (ETDEWEB)

Aspiazu, J.; Cervantes, L.; Ramirez, J.; Lopez, J.; Villasenor, P. [ININ, 52045 Ocoyoacac, Estado de Mexico (Mexico); Ramos, R.; Munoz, R. [Secretaria del Medio Ambiente, Gestion Ambiental del Aire, Mexico City (Mexico)

2007-07-01

Ball moss on Tillandsia recurvata (Bromeliaceae), collected in an area previously identified as unpolluted, was transplanted to thirteen bio-monitoring sites in the downtown and metropolitan areas of Mexico City (which cover a surface of 9,560 km{sup 2}) during the periods August 2002 - January 2003 and July 2003 - October 2003. A total of 52 lichens (weighing 300 g) were transplanted to each place. Two were analysed as zero or reference, El Chico National Park, a location 100 Km upwind from the city and the remaining 26 were hung in nylon net bags in order to be able to collect two transplanted tree month, out of every season over a one-year period. The concentrations were measured by the quantitative PIXE method based on an extemal beam facility. The atmospheric deposition for trace elements was inferred by its concentration in lichen samples collected in 2002 from 13 sites in Mexico and compared with data from a similar survey in 2003. The concentration of Cr, Cu, Co, Fe, Mn, Ni, Pb and Zn and other elements was determined for each sample. Maps for each element were drawn after a geostatistical estimate of the metal concentration in the sample was made. Maps were drawn for all elements with the estimated values. Geographical distribution patterns were obtained for the different metals, reflecting the contribution of natural and anthropogenic emission sources. The deposition patterns of V, As, Se, Cd and Pb are substantially influenced by long-range transport from other parts of Mexico City. For Cr, Fe, Co, Ni, and Cu, the deposition patterns are largely determined by contribution from point sources within Mexico and in the metropolitan area. The lichen data for Br and, in part, Se reflect an airborne supply from the environment. Contributions to trace element concentrations in lichen sources other than atmospheric deposition are identified and discussed. The Spatial and temporal variations in the distribution of metal concentration are discussed. (Author)

Temporal and spatial trends studied by lichen analysis: atmospheric deposition of trace elements in Mexico

International Nuclear Information System (INIS)

Aspiazu, J.; Cervantes, L.; Ramirez, J.; Lopez, J.; Villasenor, P.; Ramos, R.; Munoz, R.

2007-01-01

Ball moss on Tillandsia recurvata (Bromeliaceae), collected in an area previously identified as unpolluted, was transplanted to thirteen bio-monitoring sites in the downtown and metropolitan areas of Mexico City (which cover a surface of 9,560 km 2 ) during the periods August 2002 - January 2003 and July 2003 - October 2003. A total of 52 lichens (weighing 300 g) were transplanted to each place. Two were analysed as zero or reference, El Chico National Park, a location 100 Km upwind from the city and the remaining 26 were hung in nylon net bags in order to be able to collect two transplanted tree month, out of every season over a one-year period. The concentrations were measured by the quantitative PIXE method based on an extemal beam facility. The atmospheric deposition for trace elements was inferred by its concentration in lichen samples collected in 2002 from 13 sites in Mexico and compared with data from a similar survey in 2003. The concentration of Cr, Cu, Co, Fe, Mn, Ni, Pb and Zn and other elements was determined for each sample. Maps for each element were drawn after a geostatistical estimate of the metal concentration in the sample was made. Maps were drawn for all elements with the estimated values. Geographical distribution patterns were obtained for the different metals, reflecting the contribution of natural and anthropogenic emission sources. The deposition patterns of V, As, Se, Cd and Pb are substantially influenced by long-range transport from other parts of Mexico City. For Cr, Fe, Co, Ni, and Cu, the deposition patterns are largely determined by contribution from point sources within Mexico and in the metropolitan area. The lichen data for Br and, in part, Se reflect an airborne supply from the environment. Contributions to trace element concentrations in lichen sources other than atmospheric deposition are identified and discussed. The Spatial and temporal variations in the distribution of metal concentration are discussed. (Author)

NKS NordRisk. Atlas of long-range atmospheric dispersion and deposition of radionuclides from selected risk sites in the Northern Hemisphere

Energy Technology Data Exchange (ETDEWEB)

Havskov Soerensen, J.; Baklanov, A.; Mahura, A. (Danish Meteorological Institute, Copenhagen (Denmark)); Lauritzen, Bent; Mikkelsen, Torben (Technical Univ. of Denmark, Risoe National Lab. for Sustainable Energy, Roskilde (Denmark))

2008-07-15

Within the NKS NordRisk project, 'Nuclear risk from atmospheric dispersion in Northern Europe', the NKS NordRisk Atlas has been developed. The atlas describes risks from hypothetical long-range atmospheric dispersion and deposition of radionuclides from selected nuclear risk sites in the Northern Hemisphere. A number of case studies of long-term long-range atmospheric transport and deposition of radionuclides has been developed, based on two years of meteorological data. Radionuclide concentrations in air and radionuclide depositions have been evaluated and examples of long-term averages of the dispersion and deposition and of the variability around these mean values are provided. (au)

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

International Nuclear Information System (INIS)

Tateda, Yutaka; Iwao, Kenji

2008-01-01

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

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

Energy Technology Data Exchange (ETDEWEB)

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

2013-09-01

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

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

International Nuclear Information System (INIS)

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

2013-01-01

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

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

Energy Technology Data Exchange (ETDEWEB)

Cao Zongze; Yang Yuhua [Key Laboratory of Analytical Chemistry for Life Science of Shaanxi Province, School of Chemistry and Materials Science, Shaanxi Normal University, Xi' an, 710062 (China); Department of Chemistry and Biology, Ryerson University, 350 Victoria Street, Toronto, Ontario, M5B 2K3 (Canada); Lu, Julia, E-mail: julialu@ryerson.c [Department of Chemistry and Biology, Ryerson University, 350 Victoria Street, Toronto, Ontario, M5B 2K3 (Canada); Key Laboratory of Analytical Chemistry for Life Science of Shaanxi Province, School of Chemistry and Materials Science, Shaanxi Normal University, Xi' an, 710062 (China); Zhang Chengxiao, E-mail: cxzhang@snnu.edu.c [Key Laboratory of Analytical Chemistry for Life Science of Shaanxi Province, School of Chemistry and Materials Science, Shaanxi Normal University, Xi' an, 710062 (China)

2011-02-15

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{sup -2} yr{sup -1}. The average deposition rate (76.7 g m{sup -2} yr{sup -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), {approx}10% of the settled dusts having size <2.6, {approx}30% having size <10.5, and >70% having size <30 {mu}m; (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.

Improvements to the treatment of organic nitrogen chemistry & deposition in CMAQ

Science.gov (United States)

Excess atmospheric nitrogen deposition can cause significant harmful effects to ecosystems. Organic nitrogen deposition can be an important contributor to the total nitrogen budget, contributing 10-30%, however there are large uncertainties in the chemistry and deposition of thes...

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

Accounting for the effect of temperature in clarifying the response of foliar nitrogen isotope ratios to atmospheric nitrogen deposition.

Science.gov (United States)

Chen, Chongjuan; Li, Jiazhu; Wang, Guoan; Shi, Minrui

2017-12-31

Atmospheric nitrogen deposition affects nitrogen isotope composition (δ 15 N) in plants. However, both negative effect and positive effect have been reported. The effects of climate on plant δ 15 N have not been corrected for in previous studies, this has impeded discovery of a true effect of atmospheric N deposition on plant δ 15 N. To obtain a more reliable result, it is necessary to correct for the effects of climatic factors. Here, we measured δ 15 N and N contents of plants and soils in Baiwangshan and Mount Dongling, north China. Atmospheric N deposition in Baiwangshan was much higher than Mount Dongling. Generally, however, foliar N contents showed no difference between the two regions and foliar δ 15 N was significantly lower in Baiwangshan than Mount Dongling. The corrected foliar δ 15 N after accounting for a predicted value assumed to vary with temperature was obviously more negative in Baiwangshan than Mount Dongling. Thus, this suggested the necessity of temperature correction in revealing the effect of N deposition on foliar δ 15 N. Temperature, soil N sources and mycorrhizal fungi could not explain the difference in foliar δ 15 N between the two regions, this indicated that atmospheric N deposition had a negative effect on plant δ 15 N. Additionally, this study also showed that the corrected foliar δ 15 N of bulk data set increased with altitude above 1300m in Mount Dongling, this provided an another evidence for the conclusion that atmospheric N deposition could cause 15 N-depletion in plants. Copyright © 2017 Elsevier B.V. All rights reserved.

Deposition and surface characterization of nanoparticles of zinc oxide using dense plasma focus device in nitrogen atmosphere

International Nuclear Information System (INIS)

Malhotra, Yashi; Srivastava, M P; Roy, Savita

2010-01-01

Nanoparticles of zinc oxide from zinc oxide pellets in the nitrogen plasma atmosphere are deposited on n and p type silicon substrates using Dense Plasma Focus device. The hot and dense nitrogen plasma formed during the focus phase ionizes the ZnO pellet, which then move upward in a fountain like shape and gets deposited on substrates which are placed above the top of the anode. Structural and surface properties of the deposited ZnO are investigated using X-ray diffraction and Atomic force microscope (AFM). X-ray spectra shows the diffraction plane (002) of ZnO nanoparticles deposited on Si with few shots in nitrogen atmosphere. AFM investigations revealed that there are nanoparticles of size between 15-80 nm on n-Si and p-Si substrates. The deposition on n-type Si is better than the p-type Si can be seen from AFM images, this may be due to different orientation of silicon.

Two high resolution terrestrial records of atmospheric Pb deposition from New Brunswick, Canada, and Loch Laxford, Scotland

International Nuclear Information System (INIS)

Kylander, Malin E.; Weiss, Domink J.; Kober, Bernd

2009-01-01

Environmental archives like peat deposits allow for the reconstruction of both naturally and anthropogenically forced changes in the biogeochemical cycle of Pb as well as the quantification of past and present atmospheric Pb pollution. However, records of atmospheric Pb deposition from pre-industrial times are lacking. In a publication by Weiss et al. [Weiss, D., Shotyk, W., Boyle, E.A., Kramers, J.D., Appleby, P.G., Cheburkin, A.K., Comparative study of the temporal evolution of atmospheric lead deposition in Scotland and eastern Canada using blanket peat bogs. Sci Total Environ 2002;292:7-18]. Pb isotopes data measured by Q-ICP-MS and TIMS, concentration and enrichment data was presented for sites in eastern Canada (PeW1) and northwestern Scotland (LL7c), dating to 1586 A.D and 715 A.D., respectively. Here these same cores are re-analysed for Pb isotopes by MC-ICP-MS thereby acquiring 204 Pb data and improving on the original data in terms of resolution and temporal coverage. Significant differences were found between the Q-ICP-MS/TIMS and MC-ICP-MS measurements, particularly at PeW1. These discrepancies are attributed to the problematic presence of organic matter during sample preparation and analysis complicated by the heterogeneity of the organic compounds that survived sample preparation steps. The precision and accuracy of Pb isotopes in complex matrices like peat is not always well estimated by industrial standards like NIST-SRM 981 Pb. Lead pollution histories at each site were constructed using the MC-ICP-MS data. The entire LL7c record is likely subject to anthropogenic additions. Contributions from local mining were detected in Medieval times. Later, coal use and mining in Scotland, Wales and England became important. After industrialization (ca. 1885 A.D.) contributions from Broken Hill type ores and hence, leaded petrol, dominate atmospheric Pb signatures right up to modern times. At PeW1 anthropogenic impacts are first distinguishable in the late 17

Atmospheric deposition of trace elements around Ulan Bator city studied by moss and lichen biomonitoring technique and INAA

International Nuclear Information System (INIS)

Ganbold, G.; Gehrbish, Sh.; Tsehndehehkhuu, Ts.; Gundorina, S.F.; Frontas'eva, M.V.; Ostrovnaya, T.M.; Pavlov, S.S.

2005-01-01

For the first time the moss and lichen biomonitoring technique has been applied to air pollution in Mongolia (Ulan-Bator, the capital city). INAA at the IBR-2 reactor has made it possible to determine the content of 35 elements in moss and lichen biomonitors. Samples collected at sites located 10-15 km from the center of Ulan-Bator were analyzed by Instrumental Neutron Activation Analysis (INAA) using epithermal neutrons. The mosses (Rhytidium rugosum, Thuidium abietinum, Entodon concinnus) and lichens (Cladonia stellaris, Parmelia separata) were used to study the atmospheric deposition of trace elements. It was shown that the suggested types of mosses could be used as suitable biomonitors to estimate the concentration levels of heavy metals and trace elements in Ulan-Bator atmospheric deposition. The results are compared to the data of atmospheric deposition of some European countries

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

International Nuclear Information System (INIS)

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

1996-01-01

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

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

International Nuclear Information System (INIS)

Jonas, R.

1984-09-01

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

Atmospheric Deposition Effects on Plankton Communities in the Eastern Mediterranean: A Mesocosm Experimental Approach

Directory of Open Access Journals (Sweden)

Tatiana M. Tsagaraki

2017-07-01

Full Text Available The effects of atmospheric deposition on plankton community structure were examined during a mesocosm experiment using water from the Cretan Sea (Eastern Mediterranean, an area with a high frequency of atmospheric aerosol deposition events. The experiment was carried out under spring-summer conditions (May 2012. The main objective was to study the changes induced from a single deposition event, on the autotrophic and heterotrophic surface microbial populations, from viruses to zooplankton. To this end, the effects of Saharan dust addition were compared to the effects of mixed aerosol deposition on the plankton community over 9 days. The effects of the dust addition seemed to propagate throughout the food-web, with changes observed in nearly all of the measured parameters up to copepods. The dust input stimulated increased productivity, both bacterial and primary. Picoplankton, both autotrophic and heterotrophic capitalized on the changes in nutrient availability and microzooplankton abundance also increased due to increased availability of prey. Five days after the simulated deposition, copepods also responded, with an increase in egg production. The results suggest that nutrients were transported up the food web through autotrophs, which were favored by the Nitrogen supplied through both treatments. Although, the effects of individual events are generally short lived, increased deposition frequency and magnitude of events is expected in the area, due to predicted reduction in rainfall and increase in temperature, which can lead to more persistent changes in plankton community structure. Here we demonstrate how a single dust deposition event leads to enhancement of phytoplankton and microzooplankton and can eventually, through copepods, transport more nutrients up the food web in the Eastern Mediterranean Sea.

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.

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

Atmospheric Responses from Radiosonde Observations of the 2017 Total Solar Eclipse

Science.gov (United States)

Fowler, J.

2017-12-01

The Atmospheric Responses from Radiosonde Observations project during the August 21st, 2017 Total Solar Eclipse was to observe the atmospheric response under the shadow of the Moon using both research and operational earth science instruments run primarily by undergraduate students not formally trained in atmospheric science. During the eclipse, approximately 15 teams across the path of totality launched radiosonde balloon platforms in very rapid, serial sonde deployment. Our strategy was to combine a dense ground observation network with multiple radiosonde sites, located within and along the margins of the path of totality. This can demonstrate how dense observation networks leveraged among various programs can "fill the gaps" in data sparse regions allowing research ideas and questions that previously could not be approached with courser resolution data and improving the scientific understanding and prediction of geophysical and hazardous phenomenon. The core scientific objectives are (1) to make high-resolution surface and upper air observations in several sites along the eclipse path (2) to quantitatively study atmospheric responses to the rapid disappearance of the Sun across the United States, and (3) to assess the performance of high-resolution weather forecasting models in simulating the observed response. Such a scientific campaign, especially unique during a total solar eclipse, provides a rare but life-altering opportunity to attract and enable next-generation of observational scientists. It was an ideal "laboratory" for graduate, undergraduate, citizen scientists and k-12 students and staff to learn, explore and research in STEM.

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

International Nuclear Information System (INIS)

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

1989-01-01

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

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

Deposition of hybrid organic-inorganic composite coatings using an atmospheric plasma jet system.

Science.gov (United States)

Dembele, Amidou; Rahman, Mahfujur; Reid, Ian; Twomey, Barry; MacElroy, J M Don; Dowling, Denis P

2011-10-01

The objective of this study is to investigate the influence of alcohol addition on the incorporation of metal oxide nanoparticles into nm thick siloxane coatings. Titanium oxide (TiO2) nanoparticles with diameters of 30-80 nm were incorporated into an atmospheric plasma deposited tetramethylorthosilicate (TMOS) siloxane coating. The TMOS/TiO2 coating was deposited using the atmospheric plasma jet system known as PlasmaStream. In this system the liquid precursor/nanoparticle mixture is nebulised into the plasma. It was observed that prior to being nebulised the TiO2 particles agglomerated and settled over time in the TMOS/TiO2 mixture. In order to obtain a more stable nanoparticle/TMOS suspension the addition of the alcohols methanol, octanol and pentanol to this mixture was investigated. The addition of each of these alcohols was found to stabilise the nanoparticle suspension. The effect of the alcohol was therefore assessed with respect to the properties of the deposited coatings. It was observed that coatings deposited from TMOS/TiO2, with and without the addition of methanol were broadly similar. In contrast the coatings deposited with octanol and pentanol addition to the TMOS/TiO2 mixture were significantly thicker, for a given set of deposition parameters and were also more homogeneous. This would indicate that the alcohol precursor was incorporated into the plasma polymerised siloxane. The incorporation of the organic functionality from the alcohols was confirmed from FTIR spectra of the coatings. The difference in behaviour with alcohol type is likely to be due to the lower boiling point of methanol (65 degrees C), which is lower than the maximum plasma temperature measured at the jet orifice (77 degrees C). This temperature is significantly lower than the 196 degrees C and 136 degrees C boiling points of octanol and pentanol respectively. The friction of the coatings was determined using the Pin-on-disc technique. The more organic coatings deposited with

Reconstruction of historical atmospheric deposition of DDT in the Zempoala Lagoon, in the center of Mexico

Science.gov (United States)

van, Afferden M.; Hansen, A.M.; Fuller, C.C.

2005-01-01

Historical trend in deposition of DDT and its metabolites has been reconstructed by analyzing sediment cores of the Zempoala Lagoon, in the center of Mexico. The small watershed of this mountain lagoon is closed, and it is located between 2.800 and 3.700 masl. It ls neither affected by agriculture nor by permanent populations. The Zempoala Lagoon has an average depth of 3.9 mand a maximum depth of 8.8 m. Sediments were extracted with a eore sampler and analyzed by isotope methods (137CS and 2'OPb) for dating. Average sedimentation rate was determined in 0.129 9 cm" yr', corresponding to a maximum age of the 44 cm eore of approximately 60 years. The first presence of total-DDT oecurs in a depth between 28 and 32 cm of the sediment profile, corresponding to the 1960's, with a concentration of 5.3 I1g kg-'. The maximum eoncentration of total-DDT (13.0I1g kg-') occurs in sediment layers representing the late 1970's and beginning 1980's. More recently the concentration decreases towards the present concentration of 1.6 I1g kg-'. This concentration is below most DDT levels reported in recent sediment studies in the USA. The results indicate that the Zempoala Lagoon represents a natural reeipient for studies of the reconstruction of historical trends of atmospheric contaminant deposition in this region. The limitations of the methodology applied, due to the influenee of biodegradation on the definition of correct historical coneentrations of DDT depositions, are demonstrated.

Improvements to the characterization of organic nitrogen chemistry and deposition in CMAQ

Science.gov (United States)

Excess atmospheric nitrogen deposition can cause significant harmful effects to ecosystems. Organic nitrogen deposition can be an important contributor to the total nitrogen budget, contributing 10-30%, however there are large uncertainties in the chemistry and deposition of thes...

Impact of acid atmospheric deposition on soils : quantification of chemical and hydrologic processes

NARCIS (Netherlands)

Grinsven, van J.J.M.

1988-01-01

Atmospheric deposition of SO _x , NOx and NHx will cause major changes in the chemical composition of solutions in acid soils, which may affect the biological functions of the soil. This thesis deals with quantification of soil acidification by means of chemical

Atmospheric Deposition of Trace Elements Around Ulan-Bator City Studied by Moss and Lichen Biomonitoring Technique and INAA

CERN Document Server

Ganbold, G; Gundorina, S F; Frontasyeva, M V; Ostrovnaya, T M; Pavlov, S S; Tsendeekhuu, T

2005-01-01

For the first time the moss and lichen biomonitoring technique has been applied to air pollution in Mongolia (Ulan-Bator, the capital city). INAA at the IBR-2 reactor has made it possible to determine the content of 35 elements in moss and lichen biomonitors. Samples collected at sites located 10-15 km from the center of Ulan-Bator were analyzed by Instrumental Neutron Activation Analysis (INAA) using epithermal neutrons. The mosses (\\textit{Rhytidium rugosum}, \\textit{Thuidium abietinum}, \\textit{Entodon concinnus}) and lichens (\\textit{Cladonia stellaris}, \\textit{Parmelia separata}) were used to study the atmospheric deposition of trace elements. It was shown that the suggested types of mosses could be used as suitable biomonitors to estimate the concentration levels of heavy metals and trace elements in Ulan-Bator atmospheric deposition. The results are compared to the data of atmospheric deposition of some European countries.

Atmospheric Energy Deposition Modeling and Inference for Varied Meteoroid Structures

Science.gov (United States)

Wheeler, Lorien; Mathias, Donovan; Stokan, Edward; Brown, Peter

2018-01-01

Asteroids populations are highly diverse, ranging from coherent monoliths to loosely-bound rubble piles with a broad range of material and compositional properties. These different structures and properties could significantly affect how an asteroid breaks up and deposits energy in the atmosphere, and how much ground damage may occur from resulting blast waves. We have previously developed a fragment-cloud model (FCM) for assessing the atmospheric breakup and energy deposition of asteroids striking Earth. The approach represents ranges of breakup characteristics by combining progressive fragmentation with releases of variable fractions of debris and larger discrete fragments. In this work, we have extended the FCM to also represent asteroids with varied initial structures, such as rubble piles or fractured bodies. We have used the extended FCM to model the Chelyabinsk, Benesov, Kosice, and Tagish Lake meteors, and have obtained excellent matches to energy deposition profiles derived from their light curves. These matches provide validation for the FCM approach, help guide further model refinements, and enable inferences about pre-entry structure and breakup behavior. Results highlight differences in the amount of small debris vs. discrete fragments in matching the various flare characteristics of each meteor. The Chelyabinsk flares were best represented using relatively high debris fractions, while Kosice and Benesov cases were more notably driven by their discrete fragmentation characteristics, perhaps indicating more cohesive initial structures. Tagish Lake exhibited a combination of these characteristics, with lower-debris fragmentation at high altitudes followed by sudden disintegration into small debris in the lower flares. Results from all cases also suggest that lower ablation coefficients and debris spread rates may be more appropriate for the way in which debris clouds are represented in FCM, offering an avenue for future model refinement.

Lichens as biomonitors of atmospheric ammonium/ammonia deposition in Portugal

International Nuclear Information System (INIS)

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

2000-01-01

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

Assessment of atmospheric heavy metal deposition in the Tarkwa gold mining area of Ghana using epiphytic lichens

Energy Technology Data Exchange (ETDEWEB)

Boamponsem, L.K. [Department of Theoretical and Applied Biology, College of Science, Kwame Nkrumah University of Science and Technology, University Post Office, Kumasi (Ghana); Department of Laboratory Technology, School of Physical Sciences, University of Cape Coast, Cape Coast (Ghana); Adam, J.I. [Department of Theoretical and Applied Biology, College of Science, Kwame Nkrumah University of Science and Technology, University Post Office, Kumasi (Ghana); Dampare, S.B., E-mail: dampare@cc.okayama-u.ac.j [National Nuclear Research Institute, Ghana Atomic Energy Commission, P.O. Box LG 80, Legon-Accra (Ghana); Department of Earth Sciences, Okayama University, 1-1, Tsushima-Naka 3-Chome, Okayama 700-8530 (Japan); Nyarko, B.J.B. [National Nuclear Research Institute, Ghana Atomic Energy Commission, P.O. Box LG 80, Legon-Accra (Ghana); Essumang, D.K. [Department of Laboratory Technology, School of Physical Sciences, University of Cape Coast, Cape Coast (Ghana)

2010-05-01

In situ lichens (Parmelia sulcata) have been used to assess atmospheric heavy metal deposition in the Tarkwa gold mining area of Ghana. Total heavy metal concentrations obtained by instrumental neutron activation analysis (INAA) were processed by positive matrix factorization (PMF), principal component (PCA) and cluster (CA) analyses. The pollution index factor (PIF) and pollution load index (PLI) criteria revealed elevated levels of Sb, Mn, Cu, V, Al, Co, Hg, Cd and As in excess of the background values. The PCA and CA classified the examined elements into anthropogenic and natural sources, and PMF resolved three primary sources/factors: agricultural activities and other non-point anthropogenic origins, natural soil dust, and gold mining activities. Gold mining activities, which are characterized by dominant species of Sb, Th, As, Hg, Cd and Co, and significant contributions of Cu, Al, Mn and V, are the main contributors of heavy metals in the atmosphere of the study area.

Assessment of atmospheric heavy metal deposition in the Tarkwa gold mining area of Ghana using epiphytic lichens

International Nuclear Information System (INIS)

Boamponsem, L.K.; Adam, J.I.; Dampare, S.B.; Nyarko, B.J.B.; Essumang, D.K.

2010-01-01

In situ lichens (Parmelia sulcata) have been used to assess atmospheric heavy metal deposition in the Tarkwa gold mining area of Ghana. Total heavy metal concentrations obtained by instrumental neutron activation analysis (INAA) were processed by positive matrix factorization (PMF), principal component (PCA) and cluster (CA) analyses. The pollution index factor (PIF) and pollution load index (PLI) criteria revealed elevated levels of Sb, Mn, Cu, V, Al, Co, Hg, Cd and As in excess of the background values. The PCA and CA classified the examined elements into anthropogenic and natural sources, and PMF resolved three primary sources/factors: agricultural activities and other non-point anthropogenic origins, natural soil dust, and gold mining activities. Gold mining activities, which are characterized by dominant species of Sb, Th, As, Hg, Cd and Co, and significant contributions of Cu, Al, Mn and V, are the main contributors of heavy metals in the atmosphere of the study area.

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

International Nuclear Information System (INIS)

Huebschmann, W.G.; Vogt, S.

1980-01-01

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

Dynamic modelling of atmospherically-deposited Ni, Cu, Zn, Cd and Pb in Pennine catchments (northern England)

International Nuclear Information System (INIS)

Tipping, E.; Rothwell, J.J.; Shotbolt, L.; Lawlor, A.J.

2010-01-01

Simulation modelling with CHUM-AM was carried out to investigate the accumulation and release of atmospherically-deposited heavy metals (Ni, Cu, Zn, Cd and Pb) in six moorland catchments, five with organic-rich soils, one with calcareous brown earths, in the Pennine chain of northern England. The model considers two soil layers and a third layer of weathering mineral matter, and operates on a yearly timestep, driven by deposition scenarios covering the period 1400-2010. The principal processes controlling heavy metals are competitive solid-solution partitioning of solutes, chemical interactions in solution, and chemical weathering. Agreement between observed and simulated soil metal pools and surface water concentrations for recent years was generally satisfactory, the results confirming that most contemporary soil metal is from atmospheric pollution. Metals in catchments with organic-rich soils show some mobility, especially under more acid conditions, but the calcareous mineral soils have retained nearly all anthropogenic metal inputs. Complexation by dissolved organic matter and co-transport accounts for up to 80% of the Cu in surface waters. - CHUM-AM is applied to six differing moorland catchments to account for the accumulation and leaching of atmospherically-deposited trace metals over the past several centuries.

Dynamic modelling of atmospherically-deposited Ni, Cu, Zn, Cd and Pb in Pennine catchments (northern England)

Energy Technology Data Exchange (ETDEWEB)

Tipping, E., E-mail: et@ceh.ac.u [Centre for Ecology and Hydrology, Lancaster Environment Centre, Library Avenue, Bailrigg, Lancaster LA1 4AP (United Kingdom); Rothwell, J.J. [Upland Environments Research Unit, School of Environment and Development, University of Manchester, Manchester M13 9PL (United Kingdom); Shotbolt, L. [Geography Department, Queen Mary, University of London, Mile End Road, London E1 4NS (United Kingdom); Lawlor, A.J. [Centre for Ecology and Hydrology, Lancaster Environment Centre, Library Avenue, Bailrigg, Lancaster LA1 4AP (United Kingdom)

2010-05-15

Simulation modelling with CHUM-AM was carried out to investigate the accumulation and release of atmospherically-deposited heavy metals (Ni, Cu, Zn, Cd and Pb) in six moorland catchments, five with organic-rich soils, one with calcareous brown earths, in the Pennine chain of northern England. The model considers two soil layers and a third layer of weathering mineral matter, and operates on a yearly timestep, driven by deposition scenarios covering the period 1400-2010. The principal processes controlling heavy metals are competitive solid-solution partitioning of solutes, chemical interactions in solution, and chemical weathering. Agreement between observed and simulated soil metal pools and surface water concentrations for recent years was generally satisfactory, the results confirming that most contemporary soil metal is from atmospheric pollution. Metals in catchments with organic-rich soils show some mobility, especially under more acid conditions, but the calcareous mineral soils have retained nearly all anthropogenic metal inputs. Complexation by dissolved organic matter and co-transport accounts for up to 80% of the Cu in surface waters. - CHUM-AM is applied to six differing moorland catchments to account for the accumulation and leaching of atmospherically-deposited trace metals over the past several centuries.

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

Science.gov (United States)

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

2014-05-20

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

Atmospheric Metal Pollutants-Archives, Methods, and History

International Nuclear Information System (INIS)

Norton, Stephen A.

2007-01-01

Pollution of the atmosphere with cadmium (Cd), mercury (Hg), and lead (Pb) is a consequence of human activities. Natural archives are necessary to reconstruct the long-term history of metal deposition because accurate measurement of atmospheric deposition is a recent accomplishment. Reconstructions require: (1) accurate determination of concentrations of elements and isotopes, (2) accurate chronology of archives, and (3) archives that faithfully record atmosphere deposition. The most useful long-term archives are accumulations of ice and snow, peat, and lake sediment. Quantification of Cd deposition is uncommon because of its low concentration and substantial chemical mobility. Nonetheless, trends in peat and lake sediment are similar to those of Hg and Pb since ca. 1800 a.d. Both Hg and Pb are relatively chemically immobile and thus the peat and lake archives are believed to record historic trends of atmospheric deposition. Isotopic and concentration studies of Pb indicate a history of northern hemisphere atmospheric pollution extending back prior to 0 a.d. Although measurements of Hg concentration are now routine, isotopic measurements are in their infancy. Some Hg pollution sources have unique isotopic ratios, thereby contributing unique signals to the total Hg. Maximum accumulation rates of Hg and Pb occur up to 10 years later than for Cd (1970s versus 1960s in eastern North America, perhaps slightly later in Europe). By 2004, deposition of Cd, Hg, and Pb had declined from peak values in eastern North America more than 75, 75, and 90%, respectively

Resistive vs. total power depositions by Alfven modes in pre-heated low aspect ratio tokamaks

International Nuclear Information System (INIS)

Cuperman, S.; Bruma, C.; Komoshvili, K.

2004-01-01

The power deposition of fast waves launched by a LFS located antenna in a pre-heated, strongly non-uniform low aspect ratio tokamak (START) is investigated. The rigorous computational results indicate a total power deposition by far larger than that predicted for Alfven continuum eigenmodes in cylindrical plasmas. For toroidal wave numbers |N| > 1, the resistive and total power depositions are almost equal. (author)

Variability of atmospheric depositions of artificial radioelements and their transfer into soils

International Nuclear Information System (INIS)

Pourcelot, Laurent

2008-01-01

In this Habilitation thesis, I present the results and prospects of the main research topics that contribute to bettering our knowledge of the behaviour of artificial radioelements in the geosphere and biosphere. In the first chapter I present a summary of the research carried out for my thesis on the Oklo reactors. In the subsequent chapters I present my research work at the IRSN. The second chapter concerns the atmospheric depositions of radioactive contaminants. I have studied the principal environmental parameters involved in the empirical modelling of the transfer of artificial radioelements from the atmosphere to the soil. Here I essentially use measurements of artificial radioelements ( 137 Cs, plutonium, americium) in soils that reveal the variability of accidental depositions further to the Chernobyl disaster (paragraph 2.1) and chronic radioactive depositions coming from the atmospheric testing of nuclear weapons (paragraph 2.2). In the third chapter I address the problem of transfers of artificial radioelements into the soil. The interest of this lies in the fact that these transfers represent serious risks for man. Taken over the long term (in the months and years that follow the depositing of radioactive elements on the ground and plants), the transfers of radioactive pollutants into the soil are responsible for the contamination of both plants (transfer via the roots) and underground water and surface water (transfer after vertical migration). My research work into the transfers of radioactive pollutants in soils is centred on vertical migrations and root transfers, as both these processes can be studied through environmental samplings and measurements. More precisely, I have studied the migrations of radioactive pollutants and their geochemical analogues in different types of soils (paragraph 3.1) and the variability of the activities of radiostrontium and radiocesium in the compartments of permanent grassland zones (soil, grass, milk and cheese

Acid Deposition Phenomena

International Nuclear Information System (INIS)

Ramadan, A.E.K.

2004-01-01

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

Challenges in tracing the fate and effects of atmospheric polycyclic aromatic hydrocarbon deposition in vascular plants.

Science.gov (United States)

Desalme, Dorine; Binet, Philippe; Chiapusio, Geneviève

2013-05-07

Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous organic pollutants that raise environmental concerns because of their toxicity. Their accumulation in vascular plants conditions harmful consequences to human health because of their position in the food chain. Consequently, understanding how atmospheric PAHs are taken up in plant tissues is crucial for risk assessment. In this review we synthesize current knowledge about PAH atmospheric deposition, accumulation in both gymnosperms and angiosperms, mechanisms of transfer, and ecological and physiological effects. PAHs emitted in the atmosphere partition between gas and particulate phases and undergo atmospheric deposition on shoots and soil. Most PAH concentration data from vascular plant leaves suggest that contamination occurs by both direct (air-leaf) and indirect (air-soil-root) pathways. Experimental studies demonstrate that PAHs affect plant growth, interfering with plant carbon allocation and root symbioses. Photosynthesis remains the most studied physiological process affected by PAHs. Among scientific challenges, identifying specific physiological transfer mechanisms and improving the understanding of plant-symbiont interactions in relation to PAH pollution remain pivotal for both fundamental and applied environmental sciences.

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.

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

International Nuclear Information System (INIS)

Likuku, A. S.; Branford, D.

2011-01-01

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

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)

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

Science.gov (United States)

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

2017-03-01

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

New system for vacuum deposition of refractory materials using an atmospheric-pressure inductively coupled plasma

International Nuclear Information System (INIS)

Merkle, B.D.; Kniseley, R.N.; Schmidt, F.A.

1987-01-01

We have successfully developed a technique utilizing an atmospheric-pressure inductively coupled plasma combined with a low-pressure deposition chamber for deposition of thin films. The equipment and method of operation are discussed. Refractory powders (Nb and Y 2 O 3 ) were injected into the plasma and deposited as Nb and substoichiometric yttrium oxide, YO/sub 1.49/, onto Fe and Cu substrates. The substoichiometric yttrium oxide deposit adhered well to the Fe and Cu substrates, while the Nb deposit adhered well to the Fe only. The Nb deposit on the Cu substrate flaked and peeled probably because of stresses induced from the thermal expansion mismatch between the Nb and Cu. Further studies will be undertaken to better understand the processes occurring in this type of plasma-coating system in order to optimize the instrumental parameters for particular coating applications

Pre-industrial and recent (1970-2010) atmospheric deposition of sulfate and mercury in snow on southern Baffin Island, Arctic Canada.

Science.gov (United States)

Zdanowicz, Christian; Kruemmel, Eva; Lean, David; Poulain, Alexandre; Kinnard, Christophe; Yumvihoze, Emmanuel; Chen, JiuBin; Hintelmann, Holger

2015-03-15

Sulfate (SO4(2-)) and mercury (Hg) are airborne pollutants transported to the Arctic where they can affect properties of the atmosphere and the health of marine or terrestrial ecosystems. Detecting trends in Arctic Hg pollution is challenging because of the short period of direct observations, particularly of actual deposition. Here, we present an updated proxy record of atmospheric SO4(2-) and a new 40-year record of total Hg (THg) and monomethyl Hg (MeHg) deposition developed from a firn core (P2010) drilled from Penny Ice Cap, Baffin Island, Canada. The updated P2010 record shows stable mean SO4(2-) levels over the past 40 years, which is inconsistent with observations of declining atmospheric SO4(2-) or snow acidity in the Arctic during the same period. A sharp THg enhancement in the P2010 core ca 1991 is tentatively attributed to the fallout from the eruption of the Icelandic volcano Hekla. Although MeHg accumulation on Penny Ice Cap had remained constant since 1970, THg accumulation increased after the 1980s. This increase is not easily explained by changes in snow accumulation, marine aerosol inputs or air mass trajectories; however, a causal link may exist with the declining sea-ice cover conditions in the Baffin Bay sector. The ratio of THg accumulation between pre-industrial times (reconstructed from archived ice cores) and the modern industrial era is estimated at between 4- and 16-fold, which is consistent with estimates from Arctic lake sediment cores. The new P2010 THg record is the first of its kind developed from the Baffin Island region of the eastern Canadian Arctic and one of very few such records presently available in the Arctic. As such, it may help to bridge the knowledge gap linking direct observation of gaseous Hg in the Arctic atmosphere and actual net deposition and accumulation in various terrestrial media. Copyright © 2014 Elsevier B.V. All rights reserved.

Atmospheric deposition, resuspension and root uptake of plutonium in corn and other grain-producing agroecosystems near a nuclear fuel facility

International Nuclear Information System (INIS)

Pinder, J.E. III; McLeod, K.W.; Adriano, D.C.; Corey, J.C.; Boni, A.L.

1989-01-01

Plutonium released to the environment may contribute to dose to humans through inhalation or ingestion of contaminated foodstuffs. Plutonium contamination of agricultural plants may result from interception and retention of atmospheric deposition, resuspension of Pu-bearing soil particles to plant surfaces, and root uptake and translocation to grain. Plutonium on vegetation surfaces may be transferred to grain surfaces during mechanical harvesting. Data obtained from corn grown near the US Department of Energy's H-Area nuclear fuel chemical separations facility on the Savannah River Site was used to estimated parameters of a simple model of Pu transport in agroecosystems. The parameter estimates for corn were compared to those previously obtained for wheat and soybeans. Despite some differences in parameter estimates among crops, the relative importances of atmospheric deposition, resuspension and root uptake were similar among crops. For even small deposition rates, the relative importances of processes for Pu contamination of corn grain should be: transfer of atmospheric deposition from vegetation surfaces to grain surfaces during combining > resuspension of soil to grain surfaces > root uptake. Approximately 3.9 x 10 -5 of a year's atmospheric deposition is transferred to grain. Approximately 6.2 x 10 -9 of the Pu inventory in the soil is resuspended to corn grain, and a further 7.3 x 10 -10 of the soil inventory is absorbed by roots and translocated to grains

Trace organic compounds in wet atmospheric deposition: an overview

Science.gov (United States)

Steinheimer, T.R.; Johnson, S.M.

1987-01-01

An overview of the occurrence of organic compounds in wet atmospheric deposition is given. Multiplicity of sources and problems associated with source identification are discussed. Available literature is reviewed by using citations from Chemical Abstracts and Water Resources Abstracts through June 1985 and includes reports published through December 1984 that summarize current knowledge. Approaches to the chemical determination of organic compounds in precipitation are examined in addition to aspects of sampling protocols. Best methods for sample collection and preparation for instrumental analysis continue to be discussed among various investigators. Automatic wet-deposition-only devices for collection and extraction are preferred. Classes of organic compounds that have been identified in precipitation include a spectrum of compounds with differing properties of acidity or basicity, polarity, and water solubility. Those compounds that have been reported in rainfall, snowfall, and ice include hydrocarbons (both aromatic and nonaromatic), chlorinated derivatives of these hydrocarbons, carbonyl compounds (both acidic and nonacidic), and carboxylic acids and esters. Formic and acetic are the most abundant organic acids present. Cloudwater, fogwater, and mist also have been collected and analyzed for organic composition.

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.

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

Science.gov (United States)

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

2010-12-01

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

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.

Neutrons and gamma transport in atmosphere by Tripoli-2 code. Energy deposit and electron current time function

International Nuclear Information System (INIS)

Vergnaud, T.; Nimal, J.C.; Ulpat, J.P.; Faucheux, G.

1988-01-01

The Tripoli-2 computer code has been adapted to calculate, in addition to energy deposit in matter by neutrons (Kerma) the energy deposit by gamma produced in neutronic impacts and the induced recoil electron current. The energy deposit conduces at air ionization, consequently at a conductibility. This knowledge added at that of electron current permit to resolve the Maxwell equations of electromagnetic field. The study is realized for an atmospheric explosion 100 meters high. The calculations of energy deposit and electron current have been conducted as far as 2.5km [fr

Atmospheric behavior, deposition, and budget of radioactive materials from the Fukushima Daiichi nuclear power plant in March 2011

Science.gov (United States)

Morino, Y.; Ohara, T.; Nishizawa, M.

2011-12-01

To understand the atmospheric behavior of radioactive materials emitted from the Fukushima Daiichi nuclear power plant after the nuclear accident that accompanied the great Tohoku earthquake and tsunami on 11 March 2011, we simulated the transport and deposition of iodine-131 and cesium-137 using a chemical transport model. The model roughly reproduced the observed temporal and spatial variations of deposition rates over 15 Japanese prefectures (60-400 km from the plant), including Tokyo, although there were some discrepancies between the simulated and observed rates. These discrepancies were likely due to uncertainties in the simulation of emission, transport, and deposition processes in the model. A budget analysis indicated that approximately 13% of iodine-131 and 22% of cesium-137 were deposited over land in Japan, and the rest was deposited over the ocean or transported out of the model domain (700 × 700 km2). Radioactivity budgets are sensitive to temporal emission patterns. Accurate estimation of emissions to the air is important for estimation of the atmospheric behavior of radionuclides and their subsequent behavior in land water, soil, vegetation, and the ocean.

Improvements to the characterization of organic nitrogen chemistry and deposition in CMAQ (CMAS Presentation)

Science.gov (United States)

Excess atmospheric nitrogen deposition can cause significant harmful effects to ecosystems. Organic nitrogen deposition can be an important contributor to the total nitrogen budget, contributing 10-30%, however there are large uncertainties in the chemistry and deposition of thes...

Elemental tritium deposition and conversion in the terrestrial environment

International Nuclear Information System (INIS)

Dunstall, T.G.; Ogram, G.L.; Spencer, F.S.

1985-01-01

Studies were undertaken to determine the deposition and conversion of atmospheric elemental tritium in soils and vegetation. In the field tritium deposition velocities ranged between 0.007 and 0.07 cm s -1 during the summer and autumn and were less than 0.0005 cm s -1 during the winter. Deposition velocity was found to depend significantly on soil water content, total pore space and organic content in controlled laboratory experiments. In contrast to soils, exposure of vegetation to atmospheric elemental tritium resulted in negligible uptake and conversion in foliage. These studies are of significance to the assessment of behaviour and impact of elemental tritium releases

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 wet deposition of mercury and other trace elements in Pensacola, Florida

Directory of Open Access Journals (Sweden)

W. M. Landing

2010-05-01

Full Text Available In an effort to understand and quantify the impact of local, regional, and far-distant atmospheric mercury sources to rainfall mercury deposition in the Pensacola, Florida watershed, a program of event-based rainfall sampling was started in late 2004. Modified Aerochem-Metrics wet/dry rainfall samplers were deployed at three sites in the region around the Crist coal-fired power plant and event-based samples were collected continuously for three years. Samples were analyzed for total Hg and a suite of trace elements including Al, As, Ba, Bi, Cd, Ce, Co, Cr, Cs, Cu, Fe, Ga, La, Li, Mg, Mn, Na, Nb, Ni, P, Pb, Sb, Se, Si, Sn, Sr, Th, U, V, and Zn. Nutrients (ammonia and nitrate and major anions (chloride and sulfate were also measured on each sample. Multivariate statistical methods were used to sort these tracers into factors that represent potential source categories contributing to the rainfall chemistry. As, Hg, Sb, Se, Sn, and non sea-salt sulfate were all significantly correlated (R>0.6 with one factor which we interpret as an anthropogenic source term reflecting input from coal combustion throughout the southeastern US. Using ratios of total Hg to volatile elements, we estimate that 22–33% of the rainfall Hg results from coal combustion in the southeastern US with the majority coming from the global background.

Diamond synthesis at atmospheric pressure by microwave capillary plasma chemical vapor deposition

Energy Technology Data Exchange (ETDEWEB)

Hemawan, Kadek W.; Gou, Huiyang; Hemley, Russell J. [Geophysical Laboratory, Carnegie Institution of Washington, 5251 Broad Branch Rd., NW, Washington, DC 20015 (United States)

2015-11-02

Polycrystalline diamond has been synthesized on silicon substrates at atmospheric pressure, using a microwave capillary plasma chemical vapor deposition technique. The CH{sub 4}/Ar plasma was generated inside of quartz capillary tubes using 2.45 GHz microwave excitation without adding H{sub 2} into the deposition gas chemistry. Electronically excited species of CN, C{sub 2}, Ar, N{sub 2}, CH, H{sub β}, and H{sub α} were observed in the emission spectra. Raman measurements of deposited material indicate the formation of well-crystallized diamond, as evidenced by the sharp T{sub 2g} phonon at 1333 cm{sup −1} peak relative to the Raman features of graphitic carbon. Field emission scanning electron microscopy images reveal that, depending on the growth conditions, the carbon microstructures of grown films exhibit “coral” and “cauliflower-like” morphologies or well-facetted diamond crystals with grain sizes ranging from 100 nm to 10 μm.

Rapid Chemical Vapor Infiltration of Silicon Carbide Minicomposites at Atmospheric Pressure.

Science.gov (United States)

Petroski, Kenneth; Poges, Shannon; Monteleone, Chris; Grady, Joseph; Bhatt, Ram; Suib, Steven L

2018-02-07

The chemical vapor infiltration technique is one of the most popular for the fabrication of the matrix portion of a ceramic matrix composite. This work focuses on tailoring an atmospheric pressure deposition of silicon carbide onto carbon fiber tows using the methyltrichlorosilane (CH 3 SiCl 3 ) and H 2 deposition system at atmospheric pressure to create minicomposites faster than low pressure systems. Adjustment of the flow rate of H 2 bubbled through CH 3 SiCl 3 will improve the uniformity of the deposition as well as infiltrate the substrate more completely as the flow rate is decreased. Low pressure depositions conducted at 50 Torr deposit SiC at a rate of approximately 200 nm*h -1 , while the atmospheric pressure system presented has a deposition rate ranging from 750 nm*h -1 to 3.88 μm*h -1 . The minicomposites fabricated in this study had approximate total porosities of 3 and 6% for 10 and 25 SCCM infiltrations, respectively.

Long-term trends in total inorganic nitrogen and sulfur deposition in the US from 1990 to 2010

Directory of Open Access Journals (Sweden)

Y. Zhang

2018-06-01

Full Text Available Excess deposition (including both wet and dry deposition of nitrogen and sulfur is detrimental to ecosystems. Recent studies have investigated the spatial patterns and temporal trends of nitrogen and sulfur wet deposition, but few studies have focused on dry deposition due to the scarcity of dry deposition measurements. Here, we use long-term model simulations from the coupled Weather Research and Forecasting and the Community Multiscale Air Quality (WRF-CMAQ model covering the period from 1990 to 2010 to study changes in spatial distribution as well as temporal trends in total (TDEP, wet (WDEP, and dry deposition (DDEP of total inorganic nitrogen (TIN and sulfur (TS in the United States (US. We first evaluate the model's performance in simulating WDEP over the US by comparing the model results with observational data from the US National Atmospheric Deposition Program. The coupled model generally underestimates the WDEP of both TIN (including both the oxidized nitrogen deposition, TNO3, and the reduced nitrogen deposition, NHx and TS, with better performance in the eastern US than the western US. The underestimation of the wet deposition by the model is mainly caused by the coarse model grid resolution, missing lightning NOx emissions, and the poor temporal and spatial representation of NH3 emissions. TDEP of both TIN and TS shows significant decreases over the US, especially in the east, due to the large emission reductions that occurred in that region. The decreasing trends of TIN TDEP are caused by decreases in TNO3, and the increasing trends of TIN deposition over the Great Plains and Tropical Wet Forests (Southern Florida Coastal Plain regions are caused by increases in NH3 emissions, although it should be noted that these increasing trends are not significant. TIN WDEP shows decreasing trends throughout the US, except for the Marine West Coast Forest region. TIN DDEP shows significant decreasing trends in the Eastern Temperate Forests

Atmospheric deposition having been one of the major source of Pb in Jiaozhou Bay

Science.gov (United States)

Yang, Dongfang; Miao, Zhenqing; Zhang, Xiaolong; Wang, Qi; Li, Haixia

2018-03-01

Many marine bays have been polluted by Pb due to the rapid development of industry, and identifying the major source of Pb is essential to pollution control. This paper analyzed the distribution and pollution source of Pb in Jiaozhou Bay in 1988. Results showed that Pb contents in surface waters in Jiaozhou Bay in April, July and October 1988 were 5.52-24.61 μg L‑1, 7.66-38.62 μg L‑1 and 6.89-19.30 μg L‑1, respectively. The major Pb sources in this bay were atmospheric deposition, and marine current, whose source strengths were 19.30-24.61μg L‑1 and 38.62 μg L‑1, respectively. Atmospheric deposition had been one of the major Pb sources in Jiaozhou Bay, and the source strengths were stable and strong. The pollution level of Pb in this bay in 1988 was moderate to heavy, and the source control measurements were necessary.

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

International Nuclear Information System (INIS)

Stopper, S.

2001-12-01

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

Atmospheric 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.

Development of atmospheric acid deposition in China from the 1990s to the 2010s

International Nuclear Information System (INIS)

Yu, Haili; He, Nianpeng; Wang, Qiufeng; Zhu, Jianxing; Gao, Yang; Zhang, Yunhai; Jia, Yanlong; Yu, Guirui

2017-01-01

Atmospheric acid deposition is a global environmental issue. China has been experiencing serious acid deposition, which is anticipated to become more severe with the country's economic development and increasing consumption of fossil fuels in recent decades. We explored the spatiotemporal variations of acid deposition (wet acid deposition) and its influencing factors by collecting nationwide data on pH and concentrations of sulfate (SO 4 2− ) and nitrate (NO 3 − ) in precipitation between 1980 and 2014 in China. Our results showed that average precipitation pH values were 4.59 and 4.70 in the 1990s and 2010s, respectively, suggesting that precipitation acid deposition in China has not seriously worsened. Average SO 4 2− deposition declined from 40.54 to 34.87 kg S ha −1 yr −1 but average NO 3 − deposition increased from 4.44 to 7.73 kg N ha −1 yr −1 . Specifically, the area of severe precipitation acid deposition in southern China has shrunk to some extent as a result of controlling the pollutant emissions; but the area of moderate precipitation acid deposition has expanded in northern China, associated with rapid industrial and transportation development. Furthermore, we found significant positive correlations between precipitation acid deposition, energy consumption, and rainfall. Our findings provide a relatively comprehensive evaluation of the spatiotemporal dynamics of precipitation acid deposition in China over past three decades, and confirm the idea that strategies implemented to save energy and control pollutant emissions in China have been effective in alleviating precipitation acid deposition. These findings might be used to demonstrate how developing countries could achieve economic development and environmental protection through the implementation of advanced technologies to reduce pollutant emissions. - Highlights: • Explore spatial and temporal dynamics of wet acid deposition during three decades in China. • Acid

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.

Mercury Deposition Network Site Operator Training for the System Blank and Blind Audit Programs

Science.gov (United States)

Wetherbee, Gregory A.; Lehmann, Christopher M.B.

2008-01-01

The U.S. Geological Survey operates the external quality assurance project for the National Atmospheric Deposition Program/Mercury Deposition Network. The project includes the system blank and blind audit programs for assessment of total mercury concentration data quality for wet-deposition samples. This presentation was prepared to train new site operators and to refresh experienced site operators to successfully process and submit system blank and blind audit samples for chemical analysis. Analytical results are used to estimate chemical stability and contamination levels of National Atmospheric Deposition Program/Mercury Deposition Network samples and to evaluate laboratory variability and bias.

Synoptic evaluation of modelled and bioindicated atmospheric deposition of heavy metals in forests; Synoptische Auswertung modellierter atmosphaerischer Eintraege von Schwermetallen und deren Indikation durch Biomonitore in Waeldern

Energy Technology Data Exchange (ETDEWEB)

Nickel, Stefan; Schroeder, Winfried [Vechta Univ. (Germany). Lehrstuhl fuer Landschaftsoekologie; Fries, Caroline [PlanWerk - Buero fuer oekologische Fachplanungen, Nidda (Germany)

2017-03-15

Heavy metals (HM) concentrations in moss, leaves and needles and organic surface soil layers, derived from the European Moss Survey, the German Environmental Specimen Bank (ESB) and the ICP Forests were compared with those from deposition modelling by use of LOTOS-EUROS (LE) and EMEP/MSCE-HM in terms of their spatial patterns and temporal trends. The total atmospheric deposition differs considerably between the two models. HM concentrations in biomonitors (moss, leaves, and needles) were found to be predominantly higher correlated to deposition modelled by LE compared to EMEP. For Cd, strongest correlations could be found between deposition data calculated by LE and concentrations in moss (Europe, geostatistically estimated) and in needles (Germany). Regarding Pb, the coefficients of correlation came out to be the highest for EMEP deposition and measured element concentrations in moss (Europe) as well as for LE deposition and needles from ICP Forests Level II (Germany) and, respectively, leaves from ESB (Germany).

Study on the total amount control of atmospheric pollutant based on GIS.

Science.gov (United States)

Wang, Jian-Ping; Guo, Xi-Kun

2005-08-01

To provide effective environmental management for total amount control of atmospheric pollutants. An atmospheric diffusion model of sulfur dioxide on the surface of the earth was established and tested in Shantou of Guangdong Province on the basis of an overall assessment of regional natural environment, social economic state of development, pollution sources and atmospheric environmental quality. Compared with actual monitoring results in a studied region, simulation values fell within the range of two times of error and were evenly distributed in the two sides of the monitored values. Predicted with the largest emission model method, the largest emission of sulfur dioxide would be 54,279.792 tons per year in 2010. The mathematical model established and revised on the basis of GIS is more rational and suitable for the regional characteristics of total amount control of air pollutants.

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

Science.gov (United States)

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

2015-05-01

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

Atmospheric 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.

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.

Nitrogen accumulation and partitioning in a High Arctic tundra ecosystem from extreme atmospheric N deposition events

International Nuclear Information System (INIS)

Choudhary, Sonal; Blaud, Aimeric; Osborn, A. Mark; Press, Malcolm C.; Phoenix, Gareth K.

2016-01-01

Arctic ecosystems are threatened by pollution from recently detected extreme atmospheric nitrogen (N) deposition events in which up to 90% of the annual N deposition can occur in just a few days. We undertook the first assessment of the fate of N from extreme deposition in High Arctic tundra and are presenting the results from the whole ecosystem "1"5N labelling experiment. In 2010, we simulated N depositions at rates of 0, 0.04, 0.4 and 1.2 g N m"−"2 yr"−"1, applied as "1"5NH_4"1"5NO_3 in Svalbard (79"°N), during the summer. Separate applications of "1"5NO_3"− and "1"5NH_4"+ were also made to determine the importance of N form in their retention. More than 95% of the total "1"5N applied was recovered after one growing season (~ 90% after two), demonstrating a considerable capacity of Arctic tundra to retain N from these deposition events. Important sinks for the deposited N, regardless of its application rate or form, were non-vascular plants > vascular plants > organic soil > litter > mineral soil, suggesting that non-vascular plants could be the primary component of this ecosystem to undergo measurable changes due to N enrichment from extreme deposition events. Substantial retention of N by soil microbial biomass (70% and 39% of "1"5N in organic and mineral horizon, respectively) during the initial partitioning demonstrated their capacity to act as effective buffers for N leaching. Between the two N forms, vascular plants (Salix polaris) in particular showed difference in their N recovery, incorporating four times greater "1"5NO_3"− than "1"5NH_4"+, suggesting deposition rich in nitrate will impact them more. Overall, these findings show that despite the deposition rates being extreme in statistical terms, biologically they do not exceed the capacity of tundra to sequester pollutant N during the growing season. Therefore, current and future extreme events may represent a major source of eutrophication. - Highlights: • High Arctic tundra demonstrated a

Chemical cycling and deposition of atmospheric mercury in polar regions: review of recent measurements and comparison with models

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H. Angot

2016-08-01

Full Text Available Mercury (Hg is a worldwide contaminant that can cause adverse health effects to wildlife and humans. While atmospheric modeling traces the link from emissions to deposition of Hg onto environmental surfaces, large uncertainties arise from our incomplete understanding of atmospheric processes (oxidation pathways, deposition, and re-emission. Atmospheric Hg reactivity is exacerbated in high latitudes and there is still much to be learned from polar regions in terms of atmospheric processes. This paper provides a synthesis of the atmospheric Hg monitoring data available in recent years (2011–2015 in the Arctic and in Antarctica along with a comparison of these observations with numerical simulations using four cutting-edge global models. The cycle of atmospheric Hg in the Arctic and in Antarctica presents both similarities and differences. Coastal sites in the two regions are both influenced by springtime atmospheric Hg depletion events and by summertime snowpack re-emission and oceanic evasion of Hg. The cycle of atmospheric Hg differs between the two regions primarily because of their different geography. While Arctic sites are significantly influenced by northern hemispheric Hg emissions especially in winter, coastal Antarctic sites are significantly influenced by the reactivity observed on the East Antarctic ice sheet due to katabatic winds. Based on the comparison of multi-model simulations with observations, this paper discusses whether the processes that affect atmospheric Hg seasonality and interannual variability are appropriately represented in the models and identifies research gaps in our understanding of the atmospheric Hg cycling in high latitudes.

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

Directory of Open Access Journals (Sweden)

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.

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

Projecting Soil Feedbacks to Atmospheric CO2 Following Erosion and Deposition on Centennial Timescales in Two Contrasting Forests: A Study of Critical Zone-Atmosphere Exchange

Science.gov (United States)

Billings, S. A.; Richter, D., Jr.; Ziegler, S. E.; Prestegaard, K. L.

2016-12-01

For almost 20 y there has been a growing recognition that erosion and associated lateral movement of SOC does not necessarily result in a net CO2 source from terrestrial sources to the atmosphere. Eroded SOC may undergo mineralization to CO2 at a more rapid pace than it would have in situ, but the eroding ecosystem continues to generate SOC at a potentially modified rate, and the eroding profile may also experience changing SOC mineralization rates. No one knows how these process rates may change upon erosion. Years ago, we introduced a model that computes the influence of erosion on biosphere-atmosphere CO2 exchange for any profile of interest. The model permits the user to test how assumptions of changing SOC production and mineralization can influence the degree to which erosion induces a net CO2 sink or source. Here we present an analogous model depicting how deposition of eroded SOC also can result in altered biosphere-atmosphere CO2 exchange. We employ both models to investigate how erosion and deposition in two contrasting forested regions may influence regional C budgets. Runoff-induced erosion in a boreal forest occurs at low rates, but removes C-rich, organic material; anthropogenically-enhanced erosion in a warm temperate forest removed both O- and mineral-rich A-horizons. Model runs (100 y) suggest that even though the great volume of mineral soil eroded from the temperate forest was relatively low-SOC, high erosion rates prompted greater potential for erosion to serve as a net CO2 sink compared to the boreal forest where C-rich material was lost but erosion rates remained low. The models further suggest that changes in SOC production and mineralization at eroding sites in both forest types are a greater influence on CO2 source or sink strength than analogous changes at depositional sites. The fate of eroded material and the influence of erosion and deposition on SOC dynamics remain knowledge gaps critical for projecting atmospheric CO2.

Further promotion of the use of mosses and lichens for studies of atmospheric deposition of trace elements

International Nuclear Information System (INIS)

Steinnes, Eiliv

2001-01-01

Some recent and ongoing studies related to the use of mosses as biomonitors of atmospheric metal deposition are briefly reviewed. Issues discussed in particular are the conversion of concentration in moss to absolute deposition values, introduction of a second-generation ICP-MS instrument for moss analysis, determination of stable lead isotope ratios in mosses for source apportionment, and temporal trends of lead and cadmium deposition in Norway. A novel nuclear technique for the determination of fluorine in mosses surrounding an aluminium smelter is presented. (author)

Quantitative biomonitoring of nitrogen deposition with TONIS (Total N Input Biomonitoring System)

International Nuclear Information System (INIS)

Mohr, Karsten; Suda, Jerzy

2017-01-01

Monitoring of air pollutants is an important instrument to detect threats and to observe temporal trends of emissions. Determining the spatial distribution of oxidized and reduced N species via modelling requires sufficient knowledge about innumerous small sources from traffic, settlements and agriculture. Empirical studies are required to validate the model data but measurements of the total N deposition (e.g. micrometeorological measurements) are very expensive. Against this background, the TONIS, a new suitable technique which combines a biomonitoring with plants and technical measurements was developed. During 6 exposures between 2012 and 2016 at different polluted sites in Northwest Germany, TONIS accumulated between 17 and 25 kg N ha-1 yr −1 t. The results are feasible compared to simultaneously measured NH 3 and NO 2 concentration and bulk N deposition. At one site within a peat bog the accumulated N in TONIS was found to be in the range of total N deposition derived from a micrometeorological approach. - Highlights: • A new suitable biomonitoring technique is presented to determine N deposition rates relating to low-growing vegetation on nutrient-poor sites. • TONIS combines the advantages of biomonitoring and technical measurements. • The results of 6 exposures between 2012 and 2016 are feasible compared to technical measurements and modelled data.

Nitrogen deposition and its contribution to nutrient inputs to intensively managed agricultural ecosystems.

Science.gov (United States)

He, Chun-E; Wang, Xin; Liu, Xuejun; Fangmeier, Andreas; Christie, Peter; Zhang, Fusuo

2010-01-01

Interest in nitrogen inputs via atmospheric deposition to agricultural ecosystems has increased recently, especially on the North China Plain because of extremely intensive agricultural systems and rapid urbanization in this region. Nitrogen deposition may make a significant contribution to crop N requirements but may also impose a considerable nutrient burden on the environment in general. We quantified total N deposition at two locations, Dongbeiwang near Beijing and Quzhou in Hebei province, over a two-year period from 2005 to 2007 using an 15N tracer method, the integrated total N input (ITNI) system. Total airborne N inputs to a maize wheat rotation system at both locations ranged from 99 to 117 kg N x ha(-1) x yr(-1), with higher N deposition during the maize season (57-66 kg N/ha) than the wheat season (42-51 kg N/ha). Plant available N from deposition for maize and wheat was about 52 kg N x ha(-1) x yr(-1), accounting for 50% of the total N deposition or 31% of total N uptake by the two crop species. In addition, a correction factor was derived for the maize season to adjust values obtained from small pots (0.057 m2) compared with field trays (0.98 m2) because of higher plant density in the pots. The results indicate that atmospheric N deposition is a very important N input and must be taken into account when calculating nutrient budgets in very intensively managed agricultural ecosystems.

Emission, transport, deposition, and re-suspension of radionuclides from Fukushima Dai-ichi Nuclear Power Plant in the atmosphere - Overview of 2-year investigations in Japan

Science.gov (United States)

Kita, Kazuyuki; Igarashi, Yasuhiro; Yoshida, Naohiro; Nakajima, Teruyuki

2013-04-01

Following a huge earthquake and tsunami in Eastern Japan on 11 March, 2011, the accident in Fukushima Dai-ichi Nuclear Power Plant (FDNPP) occurred to emit a large amount of artificial radionuclides to the environment. Soon after the FDNPP accident, many Japanese researchers, as well as researchers in other countries, started monitoring radionuclides in various environmental fields and/or model calculations to understand extent and magnitude of radioactive pollution. In this presentation, we overview these activities for the atmospheric radionuclides in Japan as followings: 1. Investigations to evaluate radionuclide emissions by explosions at FNDPP in March 2011 and to estimate the respiration dose of the radiation at this stage. 2. Investigations to evaluate atmospheric transport and deposition processes of atmospheric radionuclide to determine the extent of radionuclide pollution. -- Based on results of the regular and urgent monitoring results, as well as the mapping of the distribution of radionuclide s accumulated by the deposition to the ground, restoration of their time-dependent emission rates has been tried, and processes determining atmospheric concentration and deposition to the ground have been investigated by using the model calculations. 3. Monitoring of the atmospheric concentrations of radionuclide after the initial, surge phase of FNDPP accident. 4. Investigations to evaluate re-suspension of radionuclide from the ground, including the soil and the vegetation. -- Intensive monitoring of the atmospheric concentrations and deposition amount of radionuclide after the initial, surge phase of the accident enable us to evaluate emission history from FNDPP, atmospheric transport and deposition processes, chemical and physical characteristics of atmospheric radionuclide especially of radio cesium, and re-suspension processes which has become dominant process to supply radio cesium to the atmosphere recently.

Potassium limits potential growth of bog vegetation under elevated atmospheric CO2 and N deposition

NARCIS (Netherlands)

Hoosbeek, M.R.; Breemen, van N.; Vasander, H.; Buttlers, A.; Berendse, F.

2002-01-01

The free air carbon dioxide enrichment (FACE) and N deposition experiments on four ombrotrophic bogs in Finland, Sweden, the Netherlands and Switzerland, revealed that after three years of treatment: (1) elevated atmospheric CO2 concentration had no significant effect on the biomass growth of

Atmospheric deposition and surface stratification as controls of contrasting chlorophyll abundance in the North Indian Ocean

Digital Repository Service at National Institute of Oceanography (India)

Patra, P.K.; DileepKumar, M.; Mahowald, N.; Sarma, V.V.S.S.

Intense upwelling during summer and convection in winter are believed to drive higher biological productivity in the Arabian Sea than in the Bay of Bengal. Although the Arabian Sea receives substantial atmospheric deposition of dust aerosols, its...

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.

Sensitivity of modeled atmospheric nitrogen species and nitrogen deposition to variations in sea salt emissions in the North Sea and Baltic Sea regions

Directory of Open Access Journals (Sweden)

D. Neumann

2016-03-01

underestimated by the model at most stations. In coastal regions, the total nitrogen deposition (wet and dry is considerably affected by sea salt particles. Approximately 3–7 % of atmospheric nitrogen deposition into the North Sea is caused by sea salt particles. The contribution is lower in the Baltic Sea region. The stations in the EMEP network provide a solid basis for model evaluation and validation. However, for a more detailed analysis of the impact of sea salt particles on atmospheric nitrogen species, size-resolved measurements of Na+, NH4+, and NO3− are needed.

Characterization of atmospheric deposition and runoff water on a small suburban catchment

OpenAIRE

LAMPREA, Diana Katerine; RUBAN, Véronique

2011-01-01

A study of air quality and atmospheric deposition on a small urban catchment (Pin Sec catchment) has been carried out in Nantes, France, in 2007 and 2008 in the frame of a federative project aimed at understanding the origin of pollution in urban environments. Carbon monoxide, nitrogen monoxide, nitrogen dioxide, ozone, sulphur dioxide and particles less than 10 µm (PM 10) were monitored for air quality, whereas heavy metals, Polycyclic aromatic hydrocarbons (PAHs) and pesticides were analyze...

Expanding atmospheric acid deposition in China from the 1990s to the 2010s

Science.gov (United States)

Yu, Haili; Wang, Qiufeng

2017-04-01

Atmospheric acid deposition is considered a global environmental issue. China has been experiencing serious acid deposition, which is anticipated to be more serious with the country's economic development and increasing consumption of fossil fuels in recent decades. By collecting nationwide data on pH and concentrations of sulfate (SO42-) and nitrate (NO3-) in precipitation between 1980 and 2014 in China, we explored the spatiotemporal variations of precipitation acid deposition (bulk deposition) and their influencing factors. Our results showed that average precipitation pH values were 4.86 and 4.84 in the 1990s and 2010s, respectively. This suggests that precipitation acid deposition in China has not seriously changes. Average SO42- deposition declined from 30.73 to 28.61 kg S ha-1 yr-1 but average NO3- deposition increased from 4.02 to 6.79 kg N ha-1 yr-1. Specifically, the area of severe precipitation acid deposition in southern China has shrunk to some extent as a result of decreasing pollutant emissions, whereas the area of moderate precipitation acid deposition has expanded in northern China, associated with rapid industrial and transportation development. Significant positive correlations have been found between precipitation acid deposition, energy consumption, and rainfall. Our findings provide a comprehensive evaluation of the spatiotemporal dynamics of precipitation acid deposition in China over past three decades, and confirm the idea that strategies implemented to save energy and reduce pollutant emissions in China have been effective in alleviating precipitation acid deposition. These findings might be used to demonstrate how developing countries could achieve economic development and environmental protection through the implementation of advanced technologies to reduce pollutant emissions.

Atmospheric Pressure Spray Chemical Vapor Deposited CuInS2 Thin Films for Photovoltaic Applications

Science.gov (United States)

Harris, J. D.; Raffaelle, R. P.; Banger, K. K.; Smith, M. A.; Scheiman, D. A.; Hepp, A. F.

2002-01-01

Solar cells have been prepared using atmospheric pressure spray chemical vapor deposited CuInS2 absorbers. The CuInS2 films were deposited at 390 C using the single source precursor (PPh3)2CuIn(SEt)4 in an argon atmosphere. The absorber ranges in thickness from 0.75 - 1.0 micrometers, and exhibits a crystallographic gradient, with the leading edge having a (220) preferred orientation and the trailing edge having a (112) orientation. Schottky diodes prepared by thermal evaporation of aluminum contacts on to the CuInS2 yielded diodes for films that were annealed at 600 C. Solar cells were prepared using annealed films and had the (top down) composition of Al/ZnO/CdS/CuInS2/Mo/Glass. The Jsc, Voc, FF and (eta) were 6.46 mA per square centimeter, 307 mV, 24% and 0.35%, respectively for the best small area cells under simulated AM0 illumination.

Wet and dry atmospheric deposition on TiO2 coated glass

International Nuclear Information System (INIS)

Chabas, Anne; Gentaz, Lucile; Lombardo, Tiziana; Sinegre, Romain; Falcone, Roberto; Verita, Marco; Cachier, Helene

2010-01-01

To prevent the soiling of glass window used in the built environment, the use TiO 2 coated products appears an important application matter. To test the cleaning efficiency and the sustainability of self-cleaning glass, a field experiment was conducted under real life condition, on a site representative of the background urban pollution. Samples of float glass, used as reference, and commercialized TiO 2 coated glasses were exposed to dry and wet atmospheric deposition during two years. The crossed optical, chemical and microscopic evaluations performed, after withdrawal, allowed highlighting a sensible difference between the reference and the self-cleaning substrate in terms of accumulation, nature, abundance and geometry of the deposit. This experiment conducted in real site emphasized on the efficacy of self-cleaning glass to reduce the maintenance cost. - This paper evaluates the self-cleaning glass efficiency highlighting its ability to prevent soiling and to be used as a mean of remediation.

Grass species influence on plant N uptake - Determination of atmospheric N deposition to a semi-natural peat bog site using a 15N labelling approach

Science.gov (United States)

Hurkuck, Miriam; Brümmer, Christian; Spott, Oliver; Flessa, Heinz; Kutsch, Werner L.

2014-05-01

Large areas of natural peat bogs in Northwestern Germany have been converted to arable land and were subjected to draining and peat cutting in the past. The few protected peatland areas remaining are affected by high nitrogen (N) deposition. Our study site - a moderately drained raised bog - is surrounded by highly fertilized agricultural land and livestock production. In this study, we used a 15N pool dilution technique called 'Integrated Total Nitrogen Input' (ITNI) to quantify annual deposition of atmospheric N into biomonitoring pots over a two-year period. Since it considers direct N uptake by plants, it was expected to result in higher N input than conventional methods for determination of N deposition (e.g. micrometeorological approaches, bulk N samplers). Using Lolium multiflorum and Eriophorum vaginatum as monitor plants and low, medium and high levels of fertilization, we aimed to simulate increasing N deposition to planted pots and to allocate airborne N after its uptake by the soil-plant system in aboveground biomass, roots and soil. Increasing N fertilization was positively correlated with biomass production of Eriophorum vaginatum, whereas atmospheric plant N uptake decreased and highest airborne N input of 899.8 ± 67.4 µg N d-1 pot-1 was found for low N fertilization. In contrast, Lolium multiflorum showed a clear dependency of N supply on plant N uptake and was highest (688.7 ± 41.4 µg N d-1 pot-1) for highly fertilized vegetation pots. Our results suggest that grass species respond differently to increasing N input. While crop grasses such as Lolium multiflorum take up N according to N availability, species adopted to nutrient-limited conditions like Eriophorum vaginatum show N saturation effects with increasing N supply. Total airborne N input ranged from about 24 to 66 kg N ha-1 yr-1 dependent on the used indicator plant and the amount of added fertilizer. Parallel determination of atmospheric N deposition using a micrometeorological approach

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

Streamwater fluxes of total mercury and methylmercury into and out of Lake Champlain

International Nuclear Information System (INIS)

Shanley, James B.; Chalmers, Ann T.

2012-01-01

From 2000 to 2004, we sampled for total mercury (THg) and methylmercury (MeHg) in inlet streams to Lake Champlain, targeting high flow periods to capture increases in THg and MeHg concentrations with increasing flow. We used these data to model stream THg and MeHg fluxes for Water Years 2001 through 2009. In this mountainous forested basin with a high watershed-to-lake area ratio of 18, fluvial export from the terrestrial watershed was the dominant source of Hg to the lake. Unfiltered THg and MeHg fluxes were dominated by the particulate fraction; about 40% of stream THg was in the filtered ( −2 yr −1 , or about 13% of atmospheric Hg wet and dry deposition to the basin. THg export from the lake represented only about 3% of atmospheric Hg input to the basin. - Highlights: ► We monitored total mercury and methylmercury in major tributaries to Lake Champlain. ► Mercury and methylmercury export was primarily as particulates during high flow. ► Only 13% of atmospheric total mercury input reached the lake via streams. ► Only 3% of atmospheric total mercury input reached the lake outlet. - Eighty-seven percent of total mercury deposition to the Lake Champlain basin is retained in the terrestrial basin; stream export of total and methylmercury to the lake is primarily in the particulate phase.

Characterization of the atmospheric pathway at hazardous waste sites

International Nuclear Information System (INIS)

Droppo, J.G. Jr.; Buck, J.W.

1988-10-01

Evaluation of potential health effects for populations surrounding hazardous waste sites requires consideration of all potential contaminant transport pathways through groundwater, surface water, and the atmosphere. A comprehensive pathway model that includes emission, dispersion, and deposition computations has been developed as a component of the Remedial Action Priority System (RAPS). RAPS is designed to assess the relative potential risks associated with hazardous and radioactive mixed-waste disposal sites. The atmospheric component includes optional volatilization and suspension emission routines. Atmospheric transport, dispersion, and deposition are computed using relatively standard modeling techniques expanded to incorporate topographical influences. This sector-averaged Gaussian model accounts for local channeling, terrain heights, and terrain roughness effects. Long-term total deposition is computed for the terrain surrounding the hazardous waste site. An example is given of applications at a US Department of Energy site, where atmospheric emissions are potentially important. The multiple applications of RAPS have provided information on the relative importance of different constitutent transport pathways from a potential population risk basis. Our results show that the atmospheric pathway is often equally as important as other pathways such as groundwater and direct soil ingestion. 6 refs., 3 figs., 4 tabs

Nitrogen accumulation and partitioning in a High Arctic tundra ecosystem from extreme atmospheric N deposition events

Energy Technology Data Exchange (ETDEWEB)

Choudhary, Sonal, E-mail: S.Choudhary@sheffield.ac.uk [Department of Animal and Plant Sciences, University of Sheffield, Western Bank, Sheffield S10 2TN (United Kingdom); Management School, University of Sheffield, Conduit Road, Sheffield S10 1FL (United Kingdom); Blaud, Aimeric [Department of Animal and Plant Sciences, University of Sheffield, Western Bank, Sheffield S10 2TN (United Kingdom); Osborn, A. Mark [Department of Animal and Plant Sciences, University of Sheffield, Western Bank, Sheffield S10 2TN (United Kingdom); School of Applied Sciences, RMIT University, PO Box 71, Bundoora, VIC 3083 (Australia); Press, Malcolm C. [School of Biosciences, University of Birmingham, Edgbaston, Birmingham B15 2TT (United Kingdom); Manchester Metropolitan University, Manchester, M15 6BH (United Kingdom); Phoenix, Gareth K. [Department of Animal and Plant Sciences, University of Sheffield, Western Bank, Sheffield S10 2TN (United Kingdom)

2016-06-01

Arctic ecosystems are threatened by pollution from recently detected extreme atmospheric nitrogen (N) deposition events in which up to 90% of the annual N deposition can occur in just a few days. We undertook the first assessment of the fate of N from extreme deposition in High Arctic tundra and are presenting the results from the whole ecosystem {sup 15}N labelling experiment. In 2010, we simulated N depositions at rates of 0, 0.04, 0.4 and 1.2 g N m{sup −2} yr{sup −1}, applied as {sup 15}NH{sub 4}{sup 15}NO{sub 3} in Svalbard (79{sup °}N), during the summer. Separate applications of {sup 15}NO{sub 3}{sup −} and {sup 15}NH{sub 4}{sup +} were also made to determine the importance of N form in their retention. More than 95% of the total {sup 15}N applied was recovered after one growing season (~ 90% after two), demonstrating a considerable capacity of Arctic tundra to retain N from these deposition events. Important sinks for the deposited N, regardless of its application rate or form, were non-vascular plants > vascular plants > organic soil > litter > mineral soil, suggesting that non-vascular plants could be the primary component of this ecosystem to undergo measurable changes due to N enrichment from extreme deposition events. Substantial retention of N by soil microbial biomass (70% and 39% of {sup 15}N in organic and mineral horizon, respectively) during the initial partitioning demonstrated their capacity to act as effective buffers for N leaching. Between the two N forms, vascular plants (Salix polaris) in particular showed difference in their N recovery, incorporating four times greater {sup 15}NO{sub 3}{sup −} than {sup 15}NH{sub 4}{sup +}, suggesting deposition rich in nitrate will impact them more. Overall, these findings show that despite the deposition rates being extreme in statistical terms, biologically they do not exceed the capacity of tundra to sequester pollutant N during the growing season. Therefore, current and future extreme events

ENVIRONMENTAL MONITORING USING LINDEN TREE LEAVES AS NATURAL TRAPS OF ATMOSPHERIC DEPOSITION: A PILOT STUDY IN TRANSILVANIA, ROMANIA

Directory of Open Access Journals (Sweden)

MIHÁLY BRAUN

2007-12-01

Full Text Available Atmospheric pollution caused by toxic elements is an emerging problem of concern. Tree leaves have been widely used as indicator of atmospheric pollutions and they are effective alternatives to the moreusual biomonitoring methods. Tree leaves can be used as natural traps of atmospheric deposition. Elemental composition of dust deposited onto leaf surfaces can be used to characterize the urban environment. A pilot survey including 16 Romanian settlements was carried out in order to evaluate the characteristics and sources of air pollutants. Tree leaves (Tilia tomentosa, Tilia cordata, Tilia platyphyllos were collected and used for the measurements. Elemental analyses were carried out by ICP-OES and ICP-MS. Principal component and discriminant analyses were used to characterizing and estimating the level of pollution. Settlements were grouped on the basis of discriminant function values. Multivariate comparison of chemical data ordered the settlements into 3 main groups, which showed a systematic geographic distribution.

Atmospheric deposition study in the area of Kardzhali lead-zinc plant based on moss analysis

International Nuclear Information System (INIS)

Hristozova, G.; Marinova, S.; Strelkova, L.P.; Goryajnova, Z.; Frontas'eva, M.V.; Stafilov, T.

2015-01-01

For the first time the moss biomonitoring technique was used to assess the environmental situation in the area affected by the lead-zinc plant as one of the most hazardous enterprises in Bulgaria. 77 Hypnum cupressiforme moss samples were collected in the Kardzhali municipality in the summer and autumn of 2011. The concentrations of a total of 47 elements were determined by means of instrumental epithermal neutron activation analysis (ENAA), atomic absorption spectrometry (AAS) and inductively coupled plasma-atomic emission spectrometry (ICP-AES). Multivariate statistics was applied to characterize the sources of elements detected in the samples. Four groups of elements were found. In comparison to the data averaged for the area outside of the town, the atmospheric deposition loads for the elements of industrial origin in Kardzhali, where the smelter chimney is located, were found to be much higher. Median levels of the measured concentrations of the most toxic metals (Pb, Zn, Cd, As, Cu, In, Sb) were extremely high in this hot spot when compared to the median Bulgarian cross-country data from the 2010-2011 European moss survey. GIS technology was used to produce element distribution maps illustrating deposition patterns of element pollutants in the study area. The results obtained contribute to the Bulgarian environmental research used to study and control the manufacturing processes of the lead-zinc plant in the town of Kardzhali.

Litter mercury deposition in the Amazonian rainforest

International Nuclear Information System (INIS)

Fostier, Anne Hélène; Melendez-Perez, José Javier; Richter, Larissa

2015-01-01

The objective of this work was to assess the flux of atmospheric mercury transferred to the soil of the Amazonian rainforest by litterfall. Calculations were based on a large survey of published and unpublished data on litterfall and Hg concentrations in litterfall samples from the Amazonian region. Litterfall based on 65 sites located in the Amazon rainforest averaged 8.15 ± 2.25 Mg ha"−"1 y"−"1. Average Hg concentrations were calculated from nine datasets for fresh tree leaves and ten datasets for litter, and a median concentration of 60.5 ng Hg g"−"1 was considered for Hg deposition in litterfall, which averaged 49 ± 14 μg m"−"2 yr"−"1. This value was used to estimate that in the Amazonian rainforest, litterfall would be responsible for the annual removing of 268 ± 77 Mg of Hg, approximately 8% of the total atmospheric Hg deposition to land. The impact of the Amazon deforestation on the Hg biogeochemical cycle is also discussed. - Highlights: • Based on published data we estimated the litterfall in the Amazonian rainforest. • All the published data on Hg concentration in leaves and litter from the region and some unpublished data are presented. • We calculated the litter mercury deposition. • We estimated the contribution of dry, wet and litter Hg deposition in the Amazonian rainforest. • We also discussed the impact of Amazon deforestation on the Hg biogeochemical cycle. - The Amazonian rainforest is responsible for removing at least 268 Mg Hg y"−"1, 8% of the total atmospheric mercury deposition to land.

Sulfur mass loading of the atmosphere from volcanic eruptions: Calibration of the ice core record on basis of sulfate aerosol deposition in polar regions from the 1982 El Chichon eruption

Science.gov (United States)

Sigurdsson, Haraldur; Laj, Paolo

1990-01-01

Major volcanic eruptions disperse large quantities of sulfur compound throughout the Earth's atmosphere. The sulfuric acid aerosols resulting from such eruptions are scavenged by snow within the polar regions and appear in polar ice cores as elevated acidity layers. Glacio-chemical studies of ice cores can, thus, provide a record of past volcanism, as well as the means for understanding the fate of volcanic sulfur in the atmosphere. The primary objectives of this project are to study the chemistry and physical properties of volcanic fallout in a Greenland Ice Core in order to evaluate the impact of the volcanic gases on the atmospheric chemistry and the total atmospheric mass of volcanic aerosols emitted by major volcanic eruptions. We propose to compare the ice core record to other atmospheric records performed during the last 10 years to investigate transport and deposition of volcanic materials.

Growth of aligned ZnO nanowires via modified atmospheric pressure chemical vapor deposition

Energy Technology Data Exchange (ETDEWEB)

Zhao, Yuping; Li, Chengchen [Faculty of Science, Jiangsu University, Zhenjiang, Jiangsu, 212013 (China); Chen, Mingming, E-mail: andychain@live.cn [Faculty of Science, Jiangsu University, Zhenjiang, Jiangsu, 212013 (China); Yu, Xiao; Chang, Yunwei [Faculty of Science, Jiangsu University, Zhenjiang, Jiangsu, 212013 (China); Chen, Anqi [State Key Laboratory of Optoelectronic Materials and Technologies, School of Electronics & Information Technology, Sun Yat-Sen University, Guangzhou Higher Education Mega Center (University Town), Guangzhou, 510006 (China); Zhu, Hai, E-mail: zhuhai5@mail.sysu.edu.cn [State Key Laboratory of Optoelectronic Materials and Technologies, School of Electronics & Information Technology, Sun Yat-Sen University, Guangzhou Higher Education Mega Center (University Town), Guangzhou, 510006 (China); Tang, Zikang, E-mail: zktang@umac.mo [State Key Laboratory of Optoelectronic Materials and Technologies, School of Electronics & Information Technology, Sun Yat-Sen University, Guangzhou Higher Education Mega Center (University Town), Guangzhou, 510006 (China); The Institute of Applied Physics and Materials Engineering, University of Macau, Avenida da Universidade, Taipa, Macau (China)

2016-12-09

In this work, we report the growth of high-quality aligned ZnO nanowires via a facile atmospheric pressure chemical vapor deposition (CVD) method. The CVD reactor chamber used was more complicated than a conventional one due to the quartz boats loaded with sources (ZnO/C) and substrates being inserted into a semi-open quartz tube, and then placed inside the CVD reactor. The semi-open quartz tube played a very important role in growing the ZnO nanowires, and demonstrated that the transportation properties of Zn and O vapor differ from those in the conventional CVD reactor chamber. Aligned ZnO nanowires were successfully obtained, though they were only found at substrates located upstream. The very high crystalline quality of the obtained ZnO nanowires was demonstrated by high-resolution transmission electron microscopy and room temperature photoluminescence investigations. Such ZnO nanowires with high crystalline quality may provide opportunities for the fabrication of ZnO-based nano-devices in future. - Highlights: • High-quality aligned ZnO nanowires were obtained via modified chemical vapor deposition under atmospheric pressure. • The semi-open quartz tube plays very important roles in growing ZnO nanowires. • The transportation properties of Zn and O vapor differ from those in the conventional CVD reactor chamber.

Growth of aligned ZnO nanowires via modified atmospheric pressure chemical vapor deposition

International Nuclear Information System (INIS)

Zhao, Yuping; Li, Chengchen; Chen, Mingming; Yu, Xiao; Chang, Yunwei; Chen, Anqi; Zhu, Hai; Tang, Zikang

2016-01-01

In this work, we report the growth of high-quality aligned ZnO nanowires via a facile atmospheric pressure chemical vapor deposition (CVD) method. The CVD reactor chamber used was more complicated than a conventional one due to the quartz boats loaded with sources (ZnO/C) and substrates being inserted into a semi-open quartz tube, and then placed inside the CVD reactor. The semi-open quartz tube played a very important role in growing the ZnO nanowires, and demonstrated that the transportation properties of Zn and O vapor differ from those in the conventional CVD reactor chamber. Aligned ZnO nanowires were successfully obtained, though they were only found at substrates located upstream. The very high crystalline quality of the obtained ZnO nanowires was demonstrated by high-resolution transmission electron microscopy and room temperature photoluminescence investigations. Such ZnO nanowires with high crystalline quality may provide opportunities for the fabrication of ZnO-based nano-devices in future. - Highlights: • High-quality aligned ZnO nanowires were obtained via modified chemical vapor deposition under atmospheric pressure. • The semi-open quartz tube plays very important roles in growing ZnO nanowires. • The transportation properties of Zn and O vapor differ from those in the conventional CVD reactor chamber.

Influence of variable rates of neritic carbonate deposition on atmospheric carbon dioxide and pelagic sediments

Science.gov (United States)

Walker, J. C.; Opdyke, B. C.

1995-01-01

Short-term imbalances in the global cycle of shallow water calcium carbonate deposition and dissolution may be responsible for much of the observed Pleistocene change in atmospheric carbon dioxide content. However, any proposed changes in the alkalinity balance of the ocean must be reconciled with the sedimentary record of deep-sea carbonates. The possible magnitude of the effect of shallow water carbonate deposition on the dissolution of pelagic carbonate can be tested using numerical simulations of the global carbon cycle. Boundary conditions can be defined by using extant shallow water carbonate accumulation data and pelagic carbonate deposition/dissolution data. On timescales of thousands of years carbonate deposition versus dissolution is rarely out of equilibrium by more than 1.5 x 10(13) mole yr-1. Results indicate that the carbonate chemistry of the ocean is rarely at equilibrium on timescales less than 10 ka. This disequilibrium is probably due to sea level-induced changes in shallow water calcium carbonate deposition/dissolution, an interpretation that does not conflict with pelagic sedimentary data from the central Pacific.

A differential absorption technique to estimate atmospheric total water vapor amounts

Science.gov (United States)

Frouin, Robert; Middleton, Elizabeth

1990-01-01

Vertically integrated water-vapor amounts can be remotely determined by measuring the solar radiance reflected by the earth's surface with satellites or aircraft-based instruments. The technique is based on the method by Fowle (1912, 1913) and utilizes the 0.940-micron water-vapor band to retrieve total-water-vapor data that is independent of surface reflectance properties and other atmospheric constituents. A channel combination is proposed to provide more accurate results, the SE-590 spectrometer is used to verify the data, and the effects of atmospheric photon backscattering is examined. The spectrometer and radiosonde data confirm the accuracy of using a narrow and a wide channel centered on the same wavelength to determine water vapor amounts. The technique is suitable for cloudless conditions and can contribute to atmospheric corrections of land-surface parameters.

Particle deposition and clearance of atmospheric particles in the human respiratory tract during LACE 98

Science.gov (United States)

Bundke, U.; Hänel, G.

2003-04-01

During the LACE 98footnote{Lindenberg Aerosol Characterization Experiment, (Germany) 1998} experiment microphysical, chemical and optical properties of atmospheric particles were measured by several groups. (Bundke et al.). The particle deposition and clearance of the particles in the human respiratory tract was calculated using the ICRP (International Commission on Radiological Protection) deposition and clearance model (ICRP 1994). Particle growth as function of relative humidity outside the body was calculated from measurement data using the model introduced by Bundke et al.. Particle growth inside the body was added using a non-equilibrium particle growth model. As a result of the calculations, time series of the total dry particle mass and -size distribution were obtained for all compartments of the human respiratory tract defined by ICRP 1994. The combined ICRP deposition and clearance model was initialized for different probationers like man, woman, children of different ages and several circumstances like light work, sitting, sleeping etc. Keeping the conditions observed during LACE 98 constant a approximation of the aerosol burdens of the different compartments was calculated up to 4 years of exposure and compared to the results from Snipes et al. for the "Phoenix" and "Philadelphia" aerosol. References: footnotesize{ Bundke, U. et al.,it{Aerosol Optical Properties during the Lindenberg Aerosol Characterization Experiment (LACE 98)} ,10.1029/2000JD000188, JGR, 2002 ICRP,it{Human Respiratory Tract Model for Radiological Protection, Bd. ICRP Publication 66}, Annals of the ICRP, 24,1-3, Elsevier Science, Ocford, 1994 Snipes et al. ,it{The 1994 ICRP66 Human Respiratory Tract Model as a Tool for predicting Lung Burdens from Exposure to Environmental Aerosols}, Appl. Occup. Environ. Hyg., 12, 547-553,1997}

Radionuclides deposition over Antarctica

International Nuclear Information System (INIS)

Pourchet, M.; Magand, O.; Frezzotti, M.; Ekaykin, A.; Winther, J.-G.

2003-01-01

A detailed and comprehensive map of the distribution patterns for both natural and artificial radionuclides over Antarctica has been established. This work integrates the results of several decades of international programs focusing on the analysis of natural and artificial radionuclides in snow and ice cores from this polar region. The mean value (37±20 Bq m -2 ) of 241 Pu total deposition over 28 stations is determined from the gamma emissions of its daughter 241 Am, presenting a long half-life (432.7 yrs). Detailed profiles and distributions of 241 Pu in ice cores make it possible to clearly distinguish between the atmospheric thermonuclear tests of the fifties and sixties. Strong relationships are also found between radionuclide data ( 137 Cs with respect to 241 Pu and 210 Pb with respect to 137 Cs), make it possible to estimate the total deposition or natural fluxes of these radionuclides. Total deposition of 137 Cs over Antarctica is estimated at 760 TBq, based on results from the 90-180 deg. East sector. Given the irregular distribution of sampling sites, more ice cores and snow samples must be analyzed in other sectors of Antarctica to check the validity of this figure

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

Science.gov (United States)

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

2013-06-01

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

Modeling of Atmospheric Transport and Deposition of Heavy Metals in the Katowice Province

OpenAIRE

Uliasz, M.; Olendrzynski, K.

1996-01-01

A large part of Poland's heavy industry, notably hard coal mining, ferrous and nonferrous metallurgy and power generation, is located in the Katowice province. Therefore, this heavy industrialized region, which is populated by four million people, experiences considerable problems with air pollution. In the METKAT study launched by the International Institute for Applied Systems Analysis we attempt to model atmospheric depositions of arsenic (As), cadmium (Cd), lead (Pb) and zinc (Zn) which a...

Atomic layer deposited high-k dielectric on graphene by functionalization through atmospheric plasma treatment

Science.gov (United States)

Shin, Jeong Woo; Kang, Myung Hoon; Oh, Seongkook; Yang, Byung Chan; Seong, Kwonil; Ahn, Hyo-Sok; Lee, Tae Hoon; An, Jihwan

2018-05-01

Atomic layer-deposited (ALD) dielectric films on graphene usually show noncontinuous and rough morphology owing to the inert surface of graphene. Here, we demonstrate the deposition of thin and uniform ALD ZrO2 films with no seed layer on chemical vapor-deposited graphene functionalized by atmospheric oxygen plasma treatment. Transmission electron microscopy showed that the ALD ZrO2 films were highly crystalline, despite a low ALD temperature of 150 °C. The ALD ZrO2 film served as an effective passivation layer for graphene, which was shown by negative shifts in the Dirac voltage and the enhanced air stability of graphene field-effect transistors after ALD of ZrO2. The ALD ZrO2 film on the functionalized graphene may find use in flexible graphene electronics and biosensors owing to its low process temperature and its capacity to improve device performance and stability.

Atmospheric Plasma Deposition of SiO2 Films for Adhesion Promoting Layers on Titanium

Directory of Open Access Journals (Sweden)

Liliana Kotte

2014-12-01

Full Text Available This paper evaluates the deposition of silica layers at atmospheric pressure as a pretreatment for the structural bonding of titanium (Ti6Al4V, Ti15V3Cr3Sn3Al in comparison to an anodizing process (NaTESi process. The SiO2 film was deposited using the LARGE plasma source, a linearly extended DC arc plasma source and applying hexamethyldisiloxane (HMDSO as a precursor. The morphology of the surface was analyzed by means of SEM, while the characterization of the chemical composition of deposited plasma layers was done by XPS and FTIR. The long-term durability of bonded samples was evaluated by means of a wedge test in hot/wet condition. The almost stoichiometric SiO2 film features a good long-term stability and a high bonding strength compared to the films produced with the wet-chemical NaTESi process.

Intra-Urban Variability in Elemental Carbon Deposition to Tree Canopies

Science.gov (United States)

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

2017-12-01

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

Atmospheric aerosol in an urban area: Comparison of measurement instruments and methodologies and pulmonary deposition assessment; Aerosol atmosferico in area urbanae di misura e valutazione di deposizione polmonare

Energy Technology Data Exchange (ETDEWEB)

Berico, M; Luciani, A; Formignani, M [ENEA, Centro Ricerche Bologna (Italy). Dip. Ambiente

1996-07-01

In March 1995 a measurement campaign of atmospheric aerosol in the Bologna urban area (Italy) was carried out. A transportable laboratory, set up by ENEA (Italian national Agency for New Technologies, Energy and the Environment) Environmental Department (Bologna), was utilized with instruments for measurement of atmospheric aerosol and meteorological parameters. The aim of this campaign was of dual purpose: to characterize aerosol in urban area and to compare different instruments and methodologies of measurements. Mass concentrations measurements, evaluated on a 23-hour period with total filter, PM10 dichotomous sampler and low pressure impactor (LPI Berner), have provided information respectively about total suspended particles, respirable fraction and granulometric parameters of aerosol. Eight meteorologic parameters, number concentration of submicromic fraction of aerosol and mass concentration of micromic fraction have been continually measured. Then, in a daytime period, several number granulometries of atmospheric aerosol have also been estimated by means of diffusion battery system. Results related to different measurement methodologies and granulometric characteristics of aerosol are presented here. Pulmonary deposition of atmospheric aerosol is finally calculated, using granulometries provided by LPI Brener and ICRP 66 human respiratory tract model.

Total quality index of Agaricus bisporus mushrooms packed in modified atmosphere.

Science.gov (United States)

Djekic, Ilija; Vunduk, Jovana; Tomašević, Igor; Kozarski, Maja; Petrovic, Predrag; Niksic, Miomir; Pudja, Predrag; Klaus, Anita

2017-07-01

The aim of this study was to develop a total quality index and examine the effects of modified atmosphere packaging (MAP) on the quality of Agaricus bisporus mushrooms stored for 22 days at 4 °C. Mushrooms were packaged under three MAPs: high nitrogen packaging (HNP), low carbon dioxide packaging (LCP) and low oxygen packaging (LOP). Passive MAP with air inside initially was used as the atmosphere treatment (AIR). This research revealed two phases in quality deterioration of A. bisporus mushrooms. During the first week, most of the quality parameters were not statistically different. Thereafter, odor intensities were stronger for all four types of packaging. Color difference and browning index values showed significantly lower color changes for AIR and LOP compared with HNP and LCP mushrooms. The best total quality index was calculated for LOP, followed by LCP and AIR. The findings of this study are useful with respect to examining two-component MAPs, separating the limiting factors (O 2 and CO 2 ) and evaluating quality deterioration effects and the total quality index of A. bisporus mushrooms. © 2016 Society of Chemical Industry. © 2016 Society of Chemical Industry.

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

Science.gov (United States)

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

2017-04-15

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

The theory of the interaction of atmospheric aerosol with underlying surface

International Nuclear Information System (INIS)

Buikov, M.V.

1993-01-01

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

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

Atmospheric deposition, water-quality, and sediment data for selected lakes in Mount Rainer, North Cascades, and Olympic National Parks, Washington, 2008-10

Science.gov (United States)

Sheibley, Rich W.; Foreman, James R.; Moran, Patrick W.; Swarzenski, Peter W.

2012-01-01

To evaluate the potential effect from atmospheric deposition of nitrogen to high-elevation lakes, the U.S. Geological Survey partnered with the National Park Service to develop a "critical load" of nitrogen for sediment diatoms. A critical load is defined as the level of a given pollutant (in this case, nitrogen) at which detrimental effects to a target endpoint (sediment diatoms) result. Because sediment diatoms are considered one of the "first responders" to ecosystem changes from nitrogen, they are a sensitive indicator for nitrogen deposition changes in natural areas. This report presents atmospheric deposition, water quality, sediment geochronology, and sediment diatom data collected from July 2008 through August 2010 in support of this effort.

ATMOSPHERIC DISPERSAL AND DEPOSITION OF TEPHRA FROM A POTENTIAL VOLCANIC ERUPTION AT YUCCA MOUNTAIN, NEVADA

International Nuclear Information System (INIS)

C. Harrington

2004-01-01

The purpose of this model report is to provide documentation of the conceptual and mathematical model (Ashplume) for atmospheric dispersal and subsequent deposition of ash on the land surface from a potential volcanic eruption at Yucca Mountain, Nevada. This report also documents the ash (tephra) redistribution conceptual model. These aspects of volcanism-related dose calculation are described in the context of the entire igneous disruptive events conceptual model in ''Characterize Framework for Igneous Activity'' (BSC 2004 [DIRS 169989], Section 6.1.1). The Ashplume conceptual model accounts for incorporation and entrainment of waste fuel particles associated with a hypothetical volcanic eruption through the Yucca Mountain repository and downwind transport of contaminated tephra. The Ashplume mathematical model describes the conceptual model in mathematical terms to allow for prediction of radioactive waste/ash deposition on the ground surface given that the hypothetical eruptive event occurs. This model report also describes the conceptual model for tephra redistribution from a basaltic cinder cone. Sensitivity analyses and model validation activities for the ash dispersal and redistribution models are also presented. Analyses documented in this model report update the previous documentation of the Ashplume mathematical model and its application to the Total System Performance Assessment (TSPA) for the License Application (TSPA-LA) igneous scenarios. This model report also documents the redistribution model product outputs based on analyses to support the conceptual model. In this report, ''Ashplume'' is used when referring to the atmospheric dispersal model and ''ASHPLUME'' is used when referencing the code of that model. Two analysis and model reports provide direct inputs to this model report, namely ''Characterize Eruptive Processes at Yucca Mountain, Nevada and Number of Waste Packages Hit by Igneous Intrusion''. This model report provides direct inputs to

An Evaluation of Atmospheric-pressure Plasma for the Cost-Effective Deposition of Antireflection Coatings

Energy Technology Data Exchange (ETDEWEB)

Rob Sailer; Guruvenket Srinivasan; Kyle W. Johnson; Douglas L. Schulz

2010-04-01

Atmospheric-pressure plasma deposition (APPD) has previously been used to deposit various functional materials including polymeric surface modification layers, transparent conducting oxides, and photo catalytic materials. For many plasma polymerized coatings, reaction occurs via free radical mechanism where the high energy electrons from the plasma activate the olefinic carbon-carbon double bonds - a typical functional group in such precursors. The precursors for such systems are typically inexpensive and readily available and have been used in vacuum PECVD previously. The objectives are to investigate: (1) the effect of plasma power, gas composition and substrate temperature on the Si-based film properties using triethylsilane(TES) as the precursor; and (2) the chemical, mechanical, and optical properties of several experimental matrices based on Design of Experiment (DOE) principals. A simple APPD route has been utilized to deposit Si based films from an inexpensive precursor - Triethylsilane (TES). Preliminary results indicates formation of Si-C & Si-O and Si-O, Si-C & Si-N bonds with oxygen and nitrogen plasmas respectively. N{sub 2}-O{sub 2} plasma showed mixed trend; however oxygen remains a significant portion of all films, despite attempts to minimize exposure to atmosphere. SiN, SiC, and SiO ratios can be modified by the reaction conditions resulting in differing film properties. SE studies revealed that films with SiN bond possess refractive index higher than coatings with Si-O/Si-C bonds. Variable angle reflectance studies showed that SiOCN coatings offer AR properties; however thickness and refractive index optimization of these coatings remains necessary for application as potential AR coatings.

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

Ahead of his time: Jacob Lipman's 1930 estimate of atmospheric sulfur deposition for the conterminous United States

Science.gov (United States)

Landa, Edward R.; Shanley, James B.

2015-01-01

A 1936 New Jersey Agricultural Experiment Station Bulletin provided an early quantitative assessment of atmospheric deposition of sulfur for the United States that has been compared in this study with more recent assessments. In the early 20th century, anthropogenic sulfur additions from the atmosphere to the soil by the combustion of fossil fuels were viewed as part of the requisite nutrient supply of crops. Jacob G. Lipman, the founding editor of Soil Science, and his team at Rutgers University, made an inventory of such additions to soils of the conterminous United States during the economic depression of the 1930s as part of a federally funded project looking at nutrient balances in soils. Lipman's team gathered data compiled by the US Bureau of Mines on coal and other fuel consumption by state and calculated the corresponding amounts of sulfur emitted. Their work pioneered a method of assessment that became the norm in the 1970s to 1980s—when acid rain emerged as a national issue. Lipman's estimate of atmospheric sulfur deposition in the 1930 is in reasonable agreement with recent historic reconstructions.

Atmospheric pressure chemical vapor deposition (APCVD) grown bi-layer graphene transistor characteristics at high temperature

KAUST Repository

Qaisi, Ramy M.; Smith, Casey; Hussain, Muhammad Mustafa

2014-01-01

We report the characteristics of atmospheric chemical vapor deposition grown bilayer graphene transistors fabricated on ultra-scaled (10 nm) high-κ dielectric aluminum oxide (Al2O3) at elevated temperatures. We observed that the drive current increased by >400% as temperature increased from room temperature to 250 °C. Low gate leakage was maintained for prolonged exposure at 100 °C but increased significantly at temperatures >200 °C. These results provide important insights for considering chemical vapor deposition graphene on aluminum oxide for high temperature applications where low power and high frequency operation are required. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Atmospheric pressure chemical vapor deposition (APCVD) grown bi-layer graphene transistor characteristics at high temperature

KAUST Repository

Qaisi, Ramy M.

2014-05-15

We report the characteristics of atmospheric chemical vapor deposition grown bilayer graphene transistors fabricated on ultra-scaled (10 nm) high-κ dielectric aluminum oxide (Al2O3) at elevated temperatures. We observed that the drive current increased by >400% as temperature increased from room temperature to 250 °C. Low gate leakage was maintained for prolonged exposure at 100 °C but increased significantly at temperatures >200 °C. These results provide important insights for considering chemical vapor deposition graphene on aluminum oxide for high temperature applications where low power and high frequency operation are required. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Atmospheric mercury in northern Wisconsin: sources and species

International Nuclear Information System (INIS)

Lamborg, C.H.; Fitzgerald, W.F.; Vandal, G.M.; Rolfhus, K.R.

1995-01-01

The atmospheric chemistry, deposition and transport of mercury (Hg) in the Upper Great Lakes region is being investigated at a near-remote sampling location in northern Wisconsin. Intensive sampling over two years has been completed. A multi-phase collection strategy was used to gain insight into the processes controlling concentrations and chemical/physical speciation of atmospheric Hg. Additional chemical and physical atmospheric determinations were also made during these periods to aid in the interpretation of the Hg determinations. For example, correlations of Hg with ozone, sulfur dioxide and synopticscale meteorological features suggest a regionally discernible signal in Hg. Comparison to isosigma backward air parcel trajectories confirms this regionality and implicates the areas south, southeast and northwest of the size to be source for Hg. Particle-phase Hg (Hg p ) was found to be approximately 40% in an oxidized form, or operationally defined as reactive but was variable. Hg p and other particle constituents show significant correlation and similarity in behavior. These observations support the hypothesis that precipitation-phase Hg arises from the scavenging of atmospheric particulates bearing Hg. Observed concentrations of rain and particle-Hg fit the theoretical expectations for nucleation and below-cloud scavenging. Increases in the Hg/aerosol mass ratio appear to take place during transport. Enrichment of aerosols is taken as evidence of gas/particle conversion which could represent the step linking gas-phase Hg with rain. The refined budget indicates ca. 24% of total deposition is from summer particle dry deposition, and that this deposition also contributes ca. 24% of all reactive Hg deposition. Most deposition occurs during the summer months. 40 refs., 4 figs., 7 tabs

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

Model analyses of atmospheric mercury: present air quality and effects of transpacific transport on the United States

Science.gov (United States)

Lei, H.; Liang, X.-Z.; Wuebbles, D. J.; Tao, Z.

2013-11-01

Atmospheric mercury is a toxic air and water pollutant that is of significant concern because of its effects on human health and ecosystems. A mechanistic representation of the atmospheric mercury cycle is developed for the state-of-the-art global climate-chemistry model, CAM-Chem (Community Atmospheric Model with Chemistry). The model simulates the emission, transport, transformation and deposition of atmospheric mercury (Hg) in three forms: elemental mercury (Hg(0)), reactive mercury (Hg(II)), and particulate mercury (PHg). Emissions of mercury include those from human, land, ocean, biomass burning and volcano related sources. Land emissions are calculated based on surface solar radiation flux and skin temperature. A simplified air-sea mercury exchange scheme is used to calculate emissions from the oceans. The chemistry mechanism includes the oxidation of Hg(0) in gaseous phase by ozone with temperature dependence, OH, H2O2 and chlorine. Aqueous chemistry includes both oxidation and reduction of Hg(0). Transport and deposition of mercury species are calculated through adapting the original formulations in CAM-Chem. The CAM-Chem model with mercury is driven by present meteorology to simulate the present mercury air quality during the 1999-2001 period. The resulting surface concentrations of total gaseous mercury (TGM) are then compared with the observations from worldwide sites. Simulated wet depositions of mercury over the continental United States are compared to the observations from 26 Mercury Deposition Network stations to test the wet deposition simulations. The evaluations of gaseous concentrations and wet deposition confirm a strong capability for the CAM-Chem mercury mechanism to simulate the atmospheric mercury cycle. The general reproduction of global TGM concentrations and the overestimation on South Africa indicate that model simulations of TGM are seriously affected by emissions. The comparison to wet deposition indicates that wet deposition patterns

A seasonal nitrogen deposition budget for Rocky Mountain National Park.

Science.gov (United States)

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

2013-07-01

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

The contribution to nitrogen deposition and ozone formation in South Norway from atmospheric emissions related to the petroleum activity in the North Sea

Energy Technology Data Exchange (ETDEWEB)

Solberg, S; Walker, S -E; Knudsen, S; Lazaridis, M; Beine, H J; Semb, A

1999-03-01

A photochemical plume model has been developed and refined. The model is designed to simulate the advection and photochemistry for several simultaneous point sources as well as the atmospheric mixing. the model has been used to calculate nitrogen deposition and ozone formation due to offshore emissions in the North Sea. Based on meteorological data for 1992 the calculations give a total contribution of 60-80 mg (N)/m{sub 2} at most in South Norway. Emission from British and Norwegian sector is calculated to contribute less than 5% each to the AOT40 index for ozone. (author)

The contribution to nitrogen deposition and ozone formation in South Norway from atmospheric emissions related to the petroleum activity in the North Sea

International Nuclear Information System (INIS)

Solberg, S.; Walker, S.-E.; Knudsen, S.; Lazaridis, M.; Beine, H.J.; Semb, A.

1999-03-01

A photochemical plume model has been developed and refined. The model is designed to simulate the advection and photochemistry for several simultaneous point sources as well as the atmospheric mixing. the model has been used to calculate nitrogen deposition and ozone formation due to offshore emissions in the North Sea. Based on meteorological data for 1992 the calculations give a total contribution of 60-80 mg (N)/m 2 at most in South Norway. Emission from British and Norwegian sector is calculated to contribute less than 5% each to the AOT40 index for ozone. (author)

Distributed emergency response system to model dispersion and deposition of atmospheric releases

International Nuclear Information System (INIS)

Taylor, S.S.

1985-04-01

Aging hardware and software and increasing commitments by the Departments of Energy and Defense have led us to develop a new, expanded system to replace the existing Atmospheric Release Advisory Capability (ARAC) system. This distributed, computer-based, emergency response system is used by state and federal agencies to assess the environmental health hazards resulting from an accidental release of radioactive material into the atmosphere. Like its predecessor, the expanded system uses local meteorology (e.g., wind speed and wind direction), as well as terrain information, to simulate the transport and dispersion of the airborne material. The system also calculates deposition and dose and displays them graphically over base maps of the local geography for use by on-site authorities. This paper discusses the limitations of the existing ARAC system. It also discusses the components and functionality of the new system, the technical difficulties encountered and resolved in its design and implementation, and the software methodologies and tools employed in its development

Fate of Deposited Nitrogen in Tropical Forests in Southern China

DEFF Research Database (Denmark)

Gurmesa, Geshere Abdisa

and denitrification from the ecosystem. Loss of N, in turn, has many negative consequences, including soil and surface water acidification, plant nutrient imbalances and related adverse effects on biological diversities. Increased atmospheric N deposition that is anticipated for tropical regions may further aggravate...... as N export in soil water in tropical forests. Total annual atmospheric deposition of N to the forest in the study period was 51 kg N ha-1yr-1. Nitrogen deposition was dominated by NH4-N due to intensive agricultural NH3 emissions in nearby areas. Nitrate dominated leaching loss from the soil...... after the last addition and by monitoring leaching of 15N in soil water on a monthly basis. The result showed that deposited N is effectively retained in plant and soil pools resembling and exceeding that observed for temperate forests. Furthermore, increased N input decreased the N retention efficiency...

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

Science.gov (United States)

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

2005-01-01

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

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

Multiscale Framework for Assessing Critical Loads of Atmospheric Nitrogen Deposition for Aquatic Ecosystems in Wilderness Areas of the Western United States

Science.gov (United States)

Nanus, Leora; Clow, David; Saros, Jasmine; McMurray, Jill; Blett, Tamara; Sickman, James

2017-04-01

High-elevation aquatic ecosystems in Wilderness areas of the western United States are impacted by current and historic 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. A predictive framework was developed for sensitive high-elevation basins across the western United States at multiple spatial scales including the Rocky Mountain Region (Rockies), the Greater Yellowstone Area (GYA), and Yosemite (YOSE) and Sequoia & Kings Canyon (SEKI) National Parks. Spatial trends in critical loads of N deposition for nutrient enrichment of aquatic ecosystems were quantified and mapped using a geostatistical approach, with modeled 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 for better quantification of uncertainty and identification of areas most sensitive to high atmospheric N deposition (> 3 kg N ha-1 yr-1). For multiple spatial scales, the lowest critical loads estimates (1.5 + 1 kg N ha-1 yr-1) correspond with areas of high N deposition and vary spatially ranging from less than 20% to over 40% of the study area for the Rockies, GYA, YOSE, and SEKI. These predictive models and maps identify sensitive aquatic ecosystems that may be impacted by excess atmospheric N deposition and can be used to help protect against future anthropogenic disturbance. The approach presented here may be transferable to other remote and protected high-elevation ecosystems at multiple spatial scales that are sensitive to adverse effects of pollutant loading in the US and around the world.

Modelling and tracer studies of atmospheric dispersion and deposition in regions of complex topography

International Nuclear Information System (INIS)

Norden, C.E.

1981-11-01

An indium tracer aerosol generating apparatus based on an alcohol/oxygen burner, and an analytical procedure by which filter samples containing tracer material could be analysed quantitatively by means of neutron activation analysis, were developed for use in atmospheric dispersion and deposition studies. A number of series of atmospheric dispersion experiments were conducted in the Richards Bay and Koeberg- Cape Town areas. The results are given, comparing the airbone tracer concentrations measured at ground level with values predicted by means of a numerical model, utilising two to three schemes, varying in sophistication, for calculating the dispersion coefficients. Recommendations are given regarding a dispersion model and dispersion coefficients for regular use in the Koeberg area, and ways for estimating plume trajectories

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.

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.

Observations of atmospheric Hg species and depositions in remote areas of China

Directory of Open Access Journals (Sweden)

Feng X.

2013-04-01

Full Text Available From September 2007, we conducted continuous measurements of speciated atmospheric mercury (Hg and atmospheric mercury depositions at five remote sites in China. Four of these sites were involved in the Global Mercury Observation System (GMOS as ground-based stations. These stations were located in the northwest, southwest, northeast, and east part of China, respectively, which represent the regional atmospheric Hg budgets in different areas of China. The preliminary results showed that mean TGM concentrations were in the range of 1.60 – 2.88 ng m-3, with relatively higher levels observed at sites in Eastern China and Southwestern China and lower levels at sites in Northeastern and Northwestern China. TGM concentrations at remote sites of China were also higher than those reported from background sites in North America and Europe, and this is corresponding very well with the Chinese great anthropogenic Hg emissions. Gaseous oxidized mercury (GOM and particulate bounded mercury (PBM were in the ranges of 3.2 – 7.4 pg m−3 and 19.4 – 43.5 pg m-3, respectively. The preliminary result on precipitation showed mean precipitation THg concentrations were in the range of 2.7 – 18.0 ng L-1.

Seasonal and diel patterns of total gaseous mercury concentration in the atmosphere of the Central Valley of Costa Rica

International Nuclear Information System (INIS)

Castillo, Aylin; Valdes, Juan; Sibaja, Jose; Vega, Ilena; Alfaro, Rosa; Morales, Jose; Esquivel, Germain; Barrantes, Elisa; Black, Paleah; Lean, David

2011-01-01

Research highlights: → Elevated seasonal and daily patterns of total gaseous mercury (TGM) were observed in the Central Valley of Costa Rica 27 km south-east of the Poas volcano. → With the onset of the wet season TGM in late April, values increased from typical values near 10 to 905 ng m -3 . → During the day, TGM values increased until midday along with temperature and radiation but relative humidity showed a reciprocal pattern. → We conclude that elemental mercury from the volcano may react with atmospheric oxidants especially during the dry season and the mercury would be deposited to the ground. → With the onset of heavy rains, mercury in the soil is reduced and re-volatilized resulting in the high levels in atmospheric air at the end of April. - Abstract: Monitoring of Hg in the atmosphere near volcanoes is limited with no previous data for Costa Rica. Seasonal and daily patterns of total gaseous mercury (TGM) were observed at the main sampling location at the Universidad Nacional, Heredia, Costa Rica. The area (lat. 10.000230 long. -84.109499) is located in the Central Valley of Costa Rica and is 27 km SE of the Poas volcano (lat. 10.199486 long. -84.231388). Measurements were made from May 2008 to May 2009 at this location with some additional values obtained at other sites near the Poas volcano including San Luis and Grecia as well as near, Turrialba and Irazu volcanoes. Total gaseous Hg was determined in samples collected at a height of 2 m using the Tekran 2537A (Tekran Inc.) gas-phase Hg vapor analyzer. Meteorological data (temperature, relative humidity, wind speed, wind direction, radiation and precipitation) were obtained from the airport weather station located at Alajuela. Monthly precipitation is typically 85 mm during the dry season (December to April) with winds from the west. The wet season begins in late April and continues to December with monthly rainfall of 328 mm and winds from the NE. The annual mean temperature is 20 deg. C

Seasonal and diel patterns of total gaseous mercury concentration in the atmosphere of the Central Valley of Costa Rica

Energy Technology Data Exchange (ETDEWEB)

Castillo, Aylin; Valdes, Juan; Sibaja, Jose; Vega, Ilena; Alfaro, Rosa; Morales, Jose; Esquivel, Germain; Barrantes, Elisa [Laboratory for Atmospheric Chemistry, LAQAT-UNA, Universidad Nacional, P.O. Box 86-3000, Heredia (Costa Rica); Black, Paleah [Department of Biology, University of Ottawa, P.O. Box 450 Station A, Ottawa, Ontario, K1N 6N5 (Canada); Lean, David, E-mail: drslean@gmail.com [P.O. Box 309, Apsley, Ontario, K0L 1A0 (Canada)

2011-02-15

Research highlights: {yields} Elevated seasonal and daily patterns of total gaseous mercury (TGM) were observed in the Central Valley of Costa Rica 27 km south-east of the Poas volcano. {yields} With the onset of the wet season TGM in late April, values increased from typical values near 10 to 905 ng m{sup -3}. {yields} During the day, TGM values increased until midday along with temperature and radiation but relative humidity showed a reciprocal pattern. {yields} We conclude that elemental mercury from the volcano may react with atmospheric oxidants especially during the dry season and the mercury would be deposited to the ground. {yields} With the onset of heavy rains, mercury in the soil is reduced and re-volatilized resulting in the high levels in atmospheric air at the end of April. - Abstract: Monitoring of Hg in the atmosphere near volcanoes is limited with no previous data for Costa Rica. Seasonal and daily patterns of total gaseous mercury (TGM) were observed at the main sampling location at the Universidad Nacional, Heredia, Costa Rica. The area (lat. 10.000230 long. -84.109499) is located in the Central Valley of Costa Rica and is 27 km SE of the Poas volcano (lat. 10.199486 long. -84.231388). Measurements were made from May 2008 to May 2009 at this location with some additional values obtained at other sites near the Poas volcano including San Luis and Grecia as well as near, Turrialba and Irazu volcanoes. Total gaseous Hg was determined in samples collected at a height of 2 m using the Tekran 2537A (Tekran Inc.) gas-phase Hg vapor analyzer. Meteorological data (temperature, relative humidity, wind speed, wind direction, radiation and precipitation) were obtained from the airport weather station located at Alajuela. Monthly precipitation is typically 85 mm during the dry season (December to April) with winds from the west. The wet season begins in late April and continues to December with monthly rainfall of 328 mm and winds from the NE. The annual mean

Spatial and temporal variation in sources of atmospheric nitrogen deposition in the Rocky Mountains using nitrogen isotopes

Science.gov (United States)

Nanus, Leora; Campbell, Donald H.; Lehmann, Christopher M. B.; Mast, M. Alisa

2018-03-01

Variation in source areas and source types of atmospheric nitrogen (N) deposition to high-elevation ecosystems in the Rocky Mountains were evaluated using spatially and temporally distributed N isotope data from atmospheric deposition networks for 1995-2016. This unique dataset links N in wet deposition and snowpack to mobile and stationary emissions sources, and enhances understanding of the impacts of anthropogenic activities and environmental policies that mitigate effects of accelerated N cycling across the Rocky Mountain region. δ15N-NO3- at 50 U.S. Geological Survey Rocky Mountain Snowpack (Snowpack) sites ranged from -3.3‰ to +6.5‰, with a mean value of +1.4‰. At 15 National Atmospheric Deposition Program (NADP)/National Trends Network wet deposition (NADP Wetfall) sites, summer δ15N-NO3- is significantly lower ranging from -7.6‰ to -1.3‰ while winter δ15N-NO3- ranges from -2.6‰ to +5.5‰, with a mean value of +0.7‰ during the cool season. The strong seasonal difference in NADP Wetfall δ15N-NO3- is due in part to variation in the proportion of N originating from source regions at different times of the year due to seasonal changes in weather patterns. Snowpack NO3- and δ15N-NO3- are significantly related to NADP Wetfall (fall and winter) suggesting that bulk snowpack samples provide a reliable estimate at high elevations. Spatial trends show higher NO3- concentrations and δ15N-NO3- in the Southern Rocky Mountains located near larger anthropogenic N emission sources compared to the Northern Rocky Mountains. NADP Wetfall δ15N-NH4+ ranged from -10‰ to 0‰, with no observed spatial pattern. However, the lowest δ15N-NH4+(-9‰), and the highest NH4+ concentration (35 μeq/L) were observed at a Utah site dominated by local agricultural activities, whereas the higher δ15N-NH4+ observed in Colorado and Wyoming are likely due to mixed sources, including fossil fuel combustion and agricultural sources. These findings show spatial and

Spatial and temporal variation in sources of atmospheric nitrogen deposition in the Rocky Mountains using nitrogen isotopes

Science.gov (United States)

Nanus, Leora; Campbell, Donald H.; Lehmann, Christopher M.B.; Mast, M. Alisa

2018-01-01

Variation in source areas and source types of atmospheric nitrogen (N) deposition to high-elevation ecosystems in the Rocky Mountains were evaluated using spatially and temporally distributed N isotope data from atmospheric deposition networks for 1995-2016. This unique dataset links N in wet deposition and snowpack to mobile and stationary emissions sources, and enhances understanding of the impacts of anthropogenic activities and environmental policies that mitigate effects of accelerated N cycling across the Rocky Mountain region. δ15N−NO3− at 50 U.S. Geological Survey Rocky Mountain Snowpack (Snowpack) sites ranged from −3.3‰ to +6.5‰, with a mean value of +1.4‰. At 15 National Atmospheric Deposition Program (NADP)/National Trends Network wet deposition (NADP Wetfall) sites, summer δ15N−NO3− is significantly lower ranging from −7.6‰ to −1.3‰ while winter δ15N−NO3− ranges from −2.6‰ to +5.5‰, with a mean value of +0.7‰ during the cool season. The strong seasonal difference in NADP Wetfall δ15N−NO3− is due in part to variation in the proportion of N originating from source regions at different times of the year due to seasonal changes in weather patterns. Snowpack NO3− and δ15N−NO3− are significantly related to NADP Wetfall (fall and winter) suggesting that bulk snowpack samples provide a reliable estimate at high elevations. Spatial trends show higher NO3−concentrations and δ15N−NO3− in the Southern Rocky Mountains located near larger anthropogenic N emission sources compared to the Northern Rocky Mountains. NADP Wetfall δ15N−NH4+ ranged from −10‰ to 0‰, with no observed spatial pattern. However, the lowest δ15N−NH4+(−9‰), and the highest NH4+ concentration (35 μeq/L) were observed at a Utah site dominated by local agricultural activities, whereas the higher δ15N−NH4+observed in Colorado and Wyoming are likely due to mixed sources, including fossil fuel combustion and

Reactive nitrogen deposition to South East Asian rainforest

Science.gov (United States)

di Marco, Chiara F.; Phillips, Gavin J.; Thomas, Rick; Tang, Sim; Nemitz, Eiko; Sutton, Mark A.; Fowler, David; Lim, Sei F.

2010-05-01

Deposition Network to estimate the total annual atmospheric reactive nitrogen deposition to this tropical forest ecosystem and to quantify the relative contribution of the different chemical compounds.

Investigation of spatial and temporal metal atmospheric deposition in France through lichen and moss bioaccumulation over one century

Energy Technology Data Exchange (ETDEWEB)

Agnan, Y., E-mail: yannick.agnan@biogeochimie.fr; Séjalon-Delmas, N.; Claustres, A.; Probst, A., E-mail: anne.probst@ensat.fr

2015-10-01

Lichens and mosses were used as biomonitors to assess the atmospheric deposition of metals in forested ecosystems in various regions of France. The concentrations of 17 metals/metalloids (Al, As, Cd, Co, Cr, Cs, Cu, Fe, Mn, Ni, Pb, Sb, Sn, Sr, Ti, V, and Zn) indicated overall low atmospheric contamination in these forested environments, but a regionalism emerged from local contributions (anthropogenic activities, as well as local lithology). Taking into account the geochemical background and comparing to Italian data, the elements from both natural and anthropogenic activities, such as Cd, Pb, or Zn, did not show any obvious anomalies. However, elements mainly originating from lithogenic dust (e.g., Al, Fe, Ti) were more prevalent in sparse forests and in the Southern regions of France, whereas samples from dense forests showed an accumulation of elements from biological recycling (Mn and Zn). The combination of enrichment factors and Pb isotope ratios between current and herbarium samples indicated the historical evolution of metal atmospheric contamination: the high contribution of coal combustion beginning 150 years ago decreased at the end of the 20th century, and the influence of car traffic during the latter observed period decreased in the last few decades. In the South of France, obvious local influences were well preserved during the last century. - Highlights: • A century of metal deposition was assessed by lichens and mosses in France. • A regional forest cover-dependent geochemical background signature was evidenced. • The anthropogenic contribution was low but stronger in the North-Eastern region. • Changes in the nature of atmospheric deposition were evidenced since the 19th century. • Pb isotopes traced a conservative specific contamination in SW France over a century.

Investigation of spatial and temporal metal atmospheric deposition in France through lichen and moss bioaccumulation over one century

International Nuclear Information System (INIS)

Agnan, Y.; Séjalon-Delmas, N.; Claustres, A.; Probst, A.

2015-01-01

Lichens and mosses were used as biomonitors to assess the atmospheric deposition of metals in forested ecosystems in various regions of France. The concentrations of 17 metals/metalloids (Al, As, Cd, Co, Cr, Cs, Cu, Fe, Mn, Ni, Pb, Sb, Sn, Sr, Ti, V, and Zn) indicated overall low atmospheric contamination in these forested environments, but a regionalism emerged from local contributions (anthropogenic activities, as well as local lithology). Taking into account the geochemical background and comparing to Italian data, the elements from both natural and anthropogenic activities, such as Cd, Pb, or Zn, did not show any obvious anomalies. However, elements mainly originating from lithogenic dust (e.g., Al, Fe, Ti) were more prevalent in sparse forests and in the Southern regions of France, whereas samples from dense forests showed an accumulation of elements from biological recycling (Mn and Zn). The combination of enrichment factors and Pb isotope ratios between current and herbarium samples indicated the historical evolution of metal atmospheric contamination: the high contribution of coal combustion beginning 150 years ago decreased at the end of the 20th century, and the influence of car traffic during the latter observed period decreased in the last few decades. In the South of France, obvious local influences were well preserved during the last century. - Highlights: • A century of metal deposition was assessed by lichens and mosses in France. • A regional forest cover-dependent geochemical background signature was evidenced. • The anthropogenic contribution was low but stronger in the North-Eastern region. • Changes in the nature of atmospheric deposition were evidenced since the 19th century. • Pb isotopes traced a conservative specific contamination in SW France over a century

Trends in atmospheric deposition fluxes of sulphur and nitrogen in Czech forests

International Nuclear Information System (INIS)

Hůnová, Iva; Maznová, Jana; Kurfürst, Pavel

2014-01-01

We present the temporal trends and spatial changes of deposition of sulphur and nitrogen in Czech forests based on records from long-term monitoring. A statistically significant trend for sulphur was detected at most of the sites measuring for wet, dry, and total deposition fluxes and at many of these the trend was also present for the period after 2000. The spatial pattern of the changes in sulphur deposition flux between 1995 and 2011 shows the decrease over the entire forested area in a wide range of 18.1–0.2 g m −2 year −1 with the most pronounced improvement in formerly most impacted regions. Nitrogen still represents a considerable stress in many areas. The value of nitrogen deposition flux of 1 g m −2 year −1 is exceeded over a significant portion of the country. On an equivalent basis, the ion ratios of NO 3 − /SO 4 2− and NH 4 + /SO 4 2− in precipitation show significantly increasing trends in time similarly to those of pH. -- Highlights: • Significant decrease of sulphur deposition at most of sites has been recorded. • Nitrogen deposition still represents a considerable stress in Czech forests. • Significantly increasing trends of NO 3 − /SO 4 2− , NH 4 + /SO 4 2− , and pH in precipitation. -- While sulphur deposition significantly decreased with the highest improvement in formerly most affected areas, nitrogen deposition still represents a considerable stress in Czech forests

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

DEFF Research Database (Denmark)

Hertel, Ole; Geels, Camilla; Frohn, Lise

2013-01-01

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

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

Science.gov (United States)

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

2015-01-01

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

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

International Nuclear Information System (INIS)

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

2000-01-01

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

Atmospheric deposition of heavy metals in Serbia studied by moss biomonitoring, neutron activation analysis and GIS technology

International Nuclear Information System (INIS)

Frontas'eva, M.V.; Galinskaya, T.E.; Pavlov, S.S.; Kumar, M.; Matavuly, M.; Radnovic, D.; Steinnes, E.

2002-01-01

The results of a pilot study on atmospheric deposition of heavy metals and other trace elements using the moss biomonitoring technique in the northern part of Serbia and some areas of Bosnia are presented. Samples of Hypnum cupressiforme along with some other moss types were collected at 92 sites during the summer of 2000. A total of 44 elements were determined by instrumental neutron activation analysis using epithermal neutrons. The observed levels of Cu, Zn, As, Ag, Cd, In, Sb, etc. in the area surrounding the town of Bor (Serbia) are comparable to those reported from similar industrial areas in other countries such as the Copper Basin in Poland and the South Urals of Russia. In the same region the maximum Se and Mo concentrations are the highest ever recorded in biomonitoring studies using mosses. High median concentrations of Fe and Ni in Serbian mosses are associated with a crustal component as apparent from factor analysis of the moss data. This component could be a result of windblown soil dust (most of the samples were taken from agricultural regions) or deposition of ash from coal-burning power stations. Some specific elements such as Cl and V may originate from known industrial sources, but at certain places high values in the moss samples are suspected to be associated with fires in oil refineries damaged during the 1999 NATO military action

Trace elements in rainwater and dry deposition around a smelting complex

Energy Technology Data Exchange (ETDEWEB)

Beavington, F

1977-06-01

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

Atmospheric deposition of heavy metals in Norway. Nationwide survey 2010

International Nuclear Information System (INIS)

Steinnes, Eiliv; Berg, Torunn; Uggerud, Hilde Thelle; Pfaffhuber, Katrine Aspmo

2011-01-01

The geographical distribution of atmospheric deposition of heavy metals in Norway was mapped in 2010 by analysis of moss samples from 464 sites all over the country. This report provides a presentation of the results and a comparison with data from a series of corresponding moss surveys starting 1977. The survey is part of an international program comprising large parts of Europe. The survey primarily concerns the ten metals of priority in the European program: vanadium, chromium, iron, nickel, copper, zinc, arsenic, cadmium, mercury, and lead. In addition data are reported for another 42 elements in the moss. The discussion of the obtained data mainly refers to contributions from air pollution. In addition influence from natural processes to the elemental composition of the moss and how it may influence the interpretation of the data is discussed. (Author)

Multielement atmospheric deposition study in Croatia using moss biomonitoring, NAA, AAS and GIS technologies

International Nuclear Information System (INIS)

Spiric, Z.; Frontas'eva, M.V.; Gundorina, S.F.; Ostrovnaya, T.M.; Stafilov, T.; Enimiteva, V.; Steinnes, E.; Bukovec, D.

2009-01-01

For the first time the moss biomonitoring technique and two complementary analytical techniques - neutron activation analysis (NAA) and atomic absorption spectrometry (AAS) - were applied to study multielement atmospheric deposition in the Republic of Croatia. Moss samples were collected during the summer 2006 from 98 sites evenly distributed over the country. Sampling was performed in accordance with the LRTAP Convention - ICP Vegetation protocol and sampling strategy of the European Programme on Biomonitoring of Heavy Metal Atmospheric Deposition. Conventional and epithermal neutron activation analyses made it possible to determine concentrations of 41 elements including key heavy metals such as Pb, Cd, Hg, and Cu determined by AAS. Principal component analysis (factor analysis with VARIMAX rotation) was applied to distinguish elements mainly of anthropogenic origin from those predominantly originating from natural sources. Geographical distribution maps of the elements over the sampled territory were constructed using GIS technology. The median values for Croatia are consistent with the corresponding values for all Europe for most elements. It was shown that the Adriatic coastline of Croatia may be considered as an environmentally pristine area. This study was conducted for providing reliable assessment of air quality throughout Croatia and producing information needed for better identification of pollution sources and improving the potential for assessing environmental and health risks in Croatia associated with toxic metals

Atmospheric deposition inputs and effects on lichen chemistry and indicator species in the Columbia River Gorge, USA

International Nuclear Information System (INIS)

Fenn, M.E.; Geiser, L.; Bachman, R.; Blubaugh, T.J.; Bytnerowicz, A.

2007-01-01

Topographic and meteorological conditions make the Columbia River Gorge (CRG) an 'exhaust pipe' for air pollutants generated by the Portland-Vancouver metropolis and Columbia Basin. We sampled fog, bulk precipitation, throughfall, airborne particulates, lichen thalli, and nitrophytic lichen distribution. Throughfall N and S deposition were high, 11.5-25.4 and 3.4-6.7 kg ha -1 over 4.5 months at all 9 and 4/9 sites, respectively. Deposition and lichen thallus N were highest at eastern- and western-most sites, implicating both agricultural and urban sources. Fog and precipitation pH were frequently as low as 3.7-5.0. Peak NO x , NH 3 , and SO 2 concentrations in the eastern CRG were low, suggesting enhanced N and S inputs were largely from particulate deposition. Lichens indicating nitrogen-enriched environments were abundant and lichen N and S concentrations were 2x higher in the CRG than surrounding national forests. The atmospheric deposition levels detected likely threaten Gorge ecosystems and cultural resources. - Nitrogen, sulfur and acidic deposition threaten natural and cultural resources in the Columbia River Gorge National Scenic Area

Huguangyan Maar Lake (SE China): A solid record of atmospheric mercury pollution history in a non-remote region

Science.gov (United States)

Zeng, Yan; Chen, Jingan; Yang, Yongqiong; Wang, Jianxu; Zhu, Zhengjie; Li, Jian

2017-10-01

Mercury is a highly toxic metal that can cause harm to environment and human health. As atmospheric deposition is the main source of total Hg input to aquatic system in remote and pristine regions, almost all the studies on atmospheric Hg pollution history concentrated in these areas, while the studies in non-remote areas are much limited, especially for the long history records. In this study, Huguangyan Maar Lake, an undisturbed lake system at low altitude in China, was selected to reconstruct the atmospheric mercury pollution history. Variation patterns of TOC, Hg and non-residual Sr in the sediment core indicated that, compared to the direct atmospheric Hg deposition, the effect of either Hg scavenging from water column by algae or the catchment inputs of previously deposited Hg on the Hg accumulation in the lake sediment was limited. The sediment Hg content in Huguangyan Lake was mainly controlled by the atmospheric Hg deposition, and thus accurately reflected the atmospheric Hg pollution history. The Hga (Hg content from atmospheric deposition) in Huguangyan Lake presented a comparable variation pattern to that in remote sites. It had the same variation trend as the global atmospheric Hg before 1950 CE, which could be attributed to the Industrial Revolution. After that, it was mainly controlled by Hg emissions from Asian countries. The variation of Hga also indicated that atmospheric Hg deposition accelerated significantly since 2000 CE. This study, along with other investigations in remote sites in China, showed that the sediment Hg in Huguangyan Lake responded to the atmospheric Hg pollution more sensitively than in the alpine regions. It should be noted that, the more intensive acceleration of Hg deposition in Huguangyan Lake may imply that the South of China suffered from much more serious atmospheric Hg pollution than previous studies revealed.

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.

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

Phytoextraction of arsenic-contaminated soil with Pteris vittata in Henan Province, China: comprehensive evaluation of remediation efficiency correcting for atmospheric depositions.

Science.gov (United States)

Lei, Mei; Wan, Xiaoming; Guo, Guanghui; Yang, Junxing; Chen, Tongbin

2018-01-01

Research on the appropriate method for evaluating phytoremediation efficiency is limited. A 2-year field experiment was conducted to investigate phytoremediation efficiency using the hyperaccumulator Pteris vittata on an arsenic (As)-contaminated site. The remediation efficiency was evaluated through the removal rate of As in soils and extraction rate of heavy metals in plants. After 2 years of remediation, the concentration of total As in soils decreased from 16.27 mg kg -1 in 2012 to 14.58 mg kg -1 in 2014. The total remediation efficiency of As was 10.39% in terms of the removal rate of heavy metals calculated for soils, whereas the remediation efficiency calculated from As uptake by P. vittata was 16.09%. Such a discrepancy aroused further consideration on the potential input of As. A large amount of As was brought in by atmospheric emissions, which possibly biased the calculation of remediation efficiency. In fact, considering also the atmospheric depositions of As, the corrected removal rate of As from soil was 16.57%. Therefore, the results of this work suggest that (i) when evaluating the phytoextraction efficiency, the whole input and output cycle of the element of interest in the targeted ecosystem must be considered, and (ii) P. vittata has the potential to be used to remediate As-contaminated soils in Henan Province, China.

ATMOSPHERIC DISPERSAL AND DEPOSITION OF TEPHRA FROM A POTENTIAL VOLCANIC ERUPTION AT YUCCA MOUNTAIN, NEVADA

Energy Technology Data Exchange (ETDEWEB)

C. Harrington

2004-10-25

The purpose of this model report is to provide documentation of the conceptual and mathematical model (Ashplume) for atmospheric dispersal and subsequent deposition of ash on the land surface from a potential volcanic eruption at Yucca Mountain, Nevada. This report also documents the ash (tephra) redistribution conceptual model. These aspects of volcanism-related dose calculation are described in the context of the entire igneous disruptive events conceptual model in ''Characterize Framework for Igneous Activity'' (BSC 2004 [DIRS 169989], Section 6.1.1). The Ashplume conceptual model accounts for incorporation and entrainment of waste fuel particles associated with a hypothetical volcanic eruption through the Yucca Mountain repository and downwind transport of contaminated tephra. The Ashplume mathematical model describes the conceptual model in mathematical terms to allow for prediction of radioactive waste/ash deposition on the ground surface given that the hypothetical eruptive event occurs. This model report also describes the conceptual model for tephra redistribution from a basaltic cinder cone. Sensitivity analyses and model validation activities for the ash dispersal and redistribution models are also presented. Analyses documented in this model report update the previous documentation of the Ashplume mathematical model and its application to the Total System Performance Assessment (TSPA) for the License Application (TSPA-LA) igneous scenarios. This model report also documents the redistribution model product outputs based on analyses to support the conceptual model. In this report, ''Ashplume'' is used when referring to the atmospheric dispersal model and ''ASHPLUME'' is used when referencing the code of that model. Two analysis and model reports provide direct inputs to this model report, namely ''Characterize Eruptive Processes at Yucca Mountain, Nevada and Number of Waste Packages Hit

Control and enhancement of the oxygen storage capacity of ceria films by variation of the deposition gas atmosphere during pulsed DC magnetron sputtering

Science.gov (United States)

Eltayeb, Asmaa; Vijayaraghavan, Rajani K.; McCoy, Anthony; Venkatanarayanan, Anita; Yaremchenko, Aleksey A.; Surendran, Rajesh; McGlynn, Enda; Daniels, Stephen

2015-04-01

In this study, nanostructured ceria (CeO2) films are deposited on Si(100) and ITO coated glass substrates by pulsed DC magnetron sputtering using a CeO2 target. The influence on the films of using various gas ambients, such as a high purity Ar and a gas mixture of high purity Ar and O2, in the sputtering chamber during deposition are studied. The film compositions are studied using XPS and SIMS. These spectra show a phase transition from cubic CeO2 to hexagonal Ce2O3 due to the sputtering process. This is related to the transformation of Ce4+ to Ce3+ and indicates a chemically reduced state of CeO2 due to the formation of oxygen vacancies. TGA and electrochemical cyclic voltammetry (CV) studies show that films deposited in an Ar atmosphere have a higher oxygen storage capacity (OSC) compared to films deposited in the presence of O2. CV results specifically show a linear variation with scan rate of the anodic peak currents for both films and the double layer capacitance values for films deposited in Ar/O2 mixed and Ar atmosphere are (1.6 ± 0.2) × 10-4 F and (4.3 ± 0.5) × 10-4 F, respectively. Also, TGA data shows that Ar sputtered samples have a tendency to greater oxygen losses upon reduction compared to the films sputtered in an Ar/O2 mixed atmosphere.

A study of wet deposition of atmospheric tritium releases at the Ontario Power Generation, Pickering Nuclear Generating Station

International Nuclear Information System (INIS)

Crooks, G.; DeWilde, J.; Yu, L.

2001-01-01

The Ontario Power Generation,Pickering Nuclear Generating Station (PNGS) has been investigating deposition of atmospheric releases of tritium on their site. This study has included numerical dispersion modelling studies conducted over the past three years, as well as an ongoing field monitoring study. The following paper will present results of the field monitoring study and make comparisons to the numerical modelling. The results of this study could be of potential use to nuclear stations in quantifying tritium deposition in near field regions where building wake effects dominate pollutant dispersion

Geochemistry of the Nsuta Mn deposit in Ghana: Implications for the Paleoproterozoic atmosphere and ocean chemistry

Science.gov (United States)

Goto, K. T.; Ito, T.; Suzuki, K.; Kashiwabara, T.; Takaya, Y.; Shimoda, G.; Nozaki, T.; Kiyokawa, S.; Tetteh, G. M.; Nyame, F. K.

2013-12-01

Oxygenation of the atmosphere and oceans has influenced the evolution of ocean chemistry and diversification of early life. A number of large manganese (Mn) deposits are distributed in the Paleoproterozoic sedimentary successions that were formed during the great oxidation event (GOE) around 2.4-2.2 Ga (Meynard, 2010). Due to the high redox potential of Mn, occurrences of Mn deposits have been regarded as important evidence for a highly oxidized environment during the Paleoproterozoic (Kirschvink et al., 2000). Furthermore, because Mn oxides strongly adsorb various elements, including bioessential elements such as Mo, formation of large Mn deposits may have affected the seawater chemical composition and ecology during the Paleoproterozoic. However, the genesis of each Mn deposit is poorly constrained, and the relationships among the formation of Mn deposits, the evolution of atmospheric and ocean chemistry, and the diversification of early life are still ambiguous. In this study, we report the Re-Os isotope compositions, rare earth element (REE) compositions, and abundance of manganophile elements in the Mn carbonate ore and host sedimentary rock samples collected from the Nsuta Mn deposit of the Birimian Supergroup, Ghana. The Nsuta deposit is one of the largest Paleoproterozoic Mn deposits, although its genesis remains controversial (Melcher et al., 1995; Mucke et al., 1999). The composite Re-Os isochron age (2149 × 130 Ma) of the Mn carbonate and sedimentary rock samples was consistent with the depositional age of the sedimentary rocks (~2.2 Ga) presumed from the U-Pb zircon age of volcanic rocks (Hirdes and Davis, 1998), suggesting that the timing of Mn ore deposition was almost equivalent to the host rock sedimentation. The PAAS-normalized REE pattern showed a positive Eu anomaly in all samples and a positive Ce anomaly only in the Mn carbonate ore. These REE patterns indicate the possible contribution of Eu-enriched fluids derived from hydrothermal activity

Acidic deposition and global climate change

International Nuclear Information System (INIS)

Nikolaidis, N.P.; Ecsedy, C.; Olem, H.; Nikolaidis, V.S.

1990-01-01

A literature is presented which examines the research published on understanding ecosystem acidification and the effects of acidic deposition on freshwaters. Topics of discussion include the following: acidic deposition; regional assessments; atmospheric deposition and transport; aquatic effects; mathematical modeling; liming acidic waters; global climate change; atmospheric changes; climate feedbacks; and aquatic effects

[Pollution Evaluation and Risk Assessment of Heavy Metals from Atmospheric Deposition in the Parks of Nanjing].

Science.gov (United States)

Wang, Cheng; Qian, Xin; Li, Hui-ming; Sun, Yi-xuan; Wang, Jin-hua

2016-05-15

Contents of heavy metals involving As, Cd, Cr, Cu, Ni, Pb and Zn from atmospheric deposition in 10 parks of Nanjing were analyzed. The pollution level, ecological risk and health risk were evaluated using Geoaccumulation Index, Potential Ecological Risk Index and the US EPA Health Risk Assessment Model, respectively. The results showed that the pollution levels of heavy metals in Swallow Rock Park, Swallow Rock Park and Mochou Lake Park were higher than the others. Compared to other cities such as Changchun, Wuhan and Beijing, the contents of heavy metals in atmospheric deposition of parks in Nanjing were higher. The evaluation results of Geoaccumulation Index showed that Pb was at moderate pollution level, Zn and Cu were between moderate and serious levels, while Cd was between serious and extreme levels. The ecological risk level of Cd was high. The assessment results of Health Risk Assessment Model indicated that there was no non-carcinogenic risk for all the seven heavy metals. For carcinogenic risk, the risks of Cd, Cr and Ni were all negligible (Risk < 1 x 10⁻⁶), whereas As had carcinogenic risk possibility but was considered to be acceptable (10⁻⁶ < Risk < 10⁻⁴).

Does nitrogen and sulfur deposition affect forest productivity?

Science.gov (United States)

Brittany A. Johnson; Kathryn B. Piatek; Mary Beth Adams; John R. Brooks

2010-01-01

We studied the effects of atmospheric nitrogen and sulfur deposition on forest productivity in a 10-year-old, aggrading forest stand at the Fernow Experimental Forest in Tucker County, WV. Forest productivity was expressed as total aboveground wood biomass, which included stem and branch weight of standing live trees. Ten years after stand regeneration and treatment...

Research Update: Atmospheric pressure spatial atomic layer deposition of ZnO thin films: Reactors, doping, and devices

Energy Technology Data Exchange (ETDEWEB)

Hoye, Robert L. Z., E-mail: rlzh2@cam.ac.uk, E-mail: jld35@cam.ac.uk; MacManus-Driscoll, Judith L., E-mail: rlzh2@cam.ac.uk, E-mail: jld35@cam.ac.uk [Department of Materials Science and Metallurgy, University of Cambridge, 27 Charles Babbage Road, Cambridge CB3 0FS (United Kingdom); Muñoz-Rojas, David [LMGP, University Grenoble-Alpes, CNRS, F-3800 Grenoble (France); Nelson, Shelby F. [Kodak Research Laboratories, Eastman Kodak Company, Rochester, New York 14650 (United States); Illiberi, Andrea; Poodt, Paul [Holst Centre/TNO Thin Film Technology, Eindhoven, 5656 AE (Netherlands); Roozeboom, Fred [Holst Centre/TNO Thin Film Technology, Eindhoven, 5656 AE (Netherlands); Department of Applied Physics, Eindhoven University of Technology, P.O. Box 513, Eindhoven, 5600 MB (Netherlands)

2015-04-01

Atmospheric pressure spatial atomic layer deposition (AP-SALD) has recently emerged as an appealing technique for rapidly producing high quality oxides. Here, we focus on the use of AP-SALD to deposit functional ZnO thin films, particularly on the reactors used, the film properties, and the dopants that have been studied. We highlight how these films are advantageous for the performance of solar cells, organometal halide perovskite light emitting diodes, and thin-film transistors. Future AP-SALD technology will enable the commercial processing of thin films over large areas on a sheet-to-sheet and roll-to-roll basis, with new reactor designs emerging for flexible plastic and paper electronics.

Application of spherical fly-ash particles to study spatial deposition of atmospheric pollutants in northen-eastern Estonia

International Nuclear Information System (INIS)

Alliksaar, T.

2000-01-01

Spherical fly-ash particles, emitted to the atmosphere in the high-temperature combustion process of fossil fuels, were found in considerable amounts in analysed snow samples of north-eastern Estonia. Spatial deposition of particles in snow cover is compared with the results of surface sediment samples of lakes. The results from snow characterise well the distribution of pollution sources and the distance from the main power plants in north eastern Estonia. Variations in particle deposition of closely situated snow samples were found to be negligible. Fly-ash particle influxes in snow samples correlate well with modelled maximum concentration fields of flyash in the near-surface air layer. (author)

Atmospheric radionuclide deposits biomonitoring in the neighbourhood of NPP Temelin in the year 2000